diff --git "a/dict_new/word_id_map.json" "b/dict_new/word_id_map.json" new file mode 100644--- /dev/null +++ "b/dict_new/word_id_map.json" @@ -0,0 +1,146928 @@ +{ + "all": [ + "HP:0000001" + ], + "abnormality of body height": [ + "HP:0000002" + ], + "multicystic kidney dysplasia": [ + "HP:0000003" + ], + "multicystic dysplastic kidney": [ + "HP:0000003" + ], + "multicystic kidney": [ + "HP:0000003" + ], + "multicystic kidneys": [ + "HP:0000003" + ], + "multicystic renal dysplasia": [ + "HP:0000003" + ], + "mode of inheritance": [ + "HP:0000005" + ], + "inheritance": [ + "HP:0000005" + ], + "autosomal dominant inheritance": [ + "HP:0000006" + ], + "autosomal dominant": [ + "HP:0000006" + ], + "autosomal dominant form": [ + "HP:0000006" + ], + "autosomal dominant type": [ + "HP:0000006" + ], + "autosomal recessive inheritance": [ + "HP:0000007" + ], + "autosomal recessive": [ + "HP:0000007" + ], + "autosomal recessive form": [ + "HP:0000007" + ], + "autosomal recessive predisposition": [ + "HP:0000007" + ], + "abnormal morphology of female internal genitalia": [ + "HP:0000008" + ], + "abnormality of female internal genitalia": [ + "HP:0000008" + ], + "functional abnormality of the bladder": [ + "HP:0000009" + ], + "poor bladder function": [ + "HP:0000009" + ], + "recurrent urinary tract infection": [ + "HP:0000010" + ], + "recurrent urinary tract infections": [ + "HP:0000010" + ], + "frequent urinary tract infection": [ + "HP:0000010" + ], + "frequent urinary tract infections": [ + "HP:0000010" + ], + "recurrent utis": [ + "HP:0000010" + ], + "repeat bladder infection": [ + "HP:0000010" + ], + "repeated bladder infections": [ + "HP:0000010" + ], + "repeat urinary tract infection": [ + "HP:0000010" + ], + "repeated urinary tract infections": [ + "HP:0000010" + ], + "urinary tract infection": [ + "HP:0000010" + ], + "urinary tract infections": [ + "HP:0000010" + ], + "urinary tract infection , recurrent": [ + "HP:0000010" + ], + "urinary tract infections , recurrent": [ + "HP:0000010" + ], + "neurogenic bladder": [ + "HP:0000011" + ], + "lack of bladder control due to nervous system injury": [ + "HP:0000011" + ], + "urinary urgency": [ + "HP:0000012" + ], + "overactive bladder": [ + "HP:0000012" + ], + "overactive bladder syndrome": [ + "HP:0000012" + ], + "urgency frequency syndrome": [ + "HP:0000012" + ], + "hypoplasia of the uterus": [ + "HP:0000013" + ], + "hypoplastic uterus": [ + "HP:0000013" + ], + "rudimentary uterus": [ + "HP:0000013" + ], + "small uterus": [ + "HP:0000013" + ], + "underdeveloped uterus": [ + "HP:0000013" + ], + "abnormality of the bladder": [ + "HP:0000014" + ], + "bladder diverticulum": [ + "HP:0000015" + ], + "bladder diverticula": [ + "HP:0000015" + ], + "urinary retention": [ + "HP:0000016" + ], + "increase post - void residual urine volume": [ + "HP:0000016" + ], + "increased post - void residual urine volume": [ + "HP:0000016" + ], + "nocturia": [ + "HP:0000017" + ], + "nycturia": [ + "HP:0000017" + ], + "urinary hesitancy": [ + "HP:0000019" + ], + "difficulty with flow": [ + "HP:0000019" + ], + "urinary incontinence": [ + "HP:0000020" + ], + "bladder incontinence": [ + "HP:0000020" + ], + "loss of bladder control": [ + "HP:0000020" + ], + "megacystis": [ + "HP:0000021" + ], + "abnormality of male internal genitalia": [ + "HP:0000022" + ], + "inguinal hernia": [ + "HP:0000023" + ], + "prostatitis": [ + "HP:0000024" + ], + "inflammation of the prostate": [ + "HP:0000024" + ], + "functional abnormality of male internal genitalia": [ + "HP:0000025" + ], + "male hypogonadism": [ + "HP:0000026" + ], + "decrease function of male gonad": [ + "HP:0000026" + ], + "decreased function of male gonad": [ + "HP:0000026" + ], + "azoospermia": [ + "HP:0000027" + ], + "absent sperm in semen": [ + "HP:0000027" + ], + "cryptorchidism": [ + "HP:0000028" + ], + "cryptorchism": [ + "HP:0000028" + ], + "undescended testis": [ + "HP:0000028" + ], + "undescended testes": [ + "HP:0000028" + ], + "testicular atrophy": [ + "HP:0000029" + ], + "testicular degeneration": [ + "HP:0000029" + ], + "testicular gonadoblastoma": [ + "HP:0000030" + ], + "gonadoblastoma , male": [ + "HP:0000030" + ], + "epididymitis": [ + "HP:0000031" + ], + "abnormality of male external genitalia": [ + "HP:0000032" + ], + "ambiguous genitalia , male": [ + "HP:0000033" + ], + "ambiguous genitalia in male": [ + "HP:0000033" + ], + "ambiguous genitalia in males": [ + "HP:0000033" + ], + "hydrocele testis": [ + "HP:0000034" + ], + "hydrocele": [ + "HP:0000034" + ], + "testicular hydrocele": [ + "HP:0000034" + ], + "abnormal testis morphology": [ + "HP:0000035" + ], + "abnormality of the testis": [ + "HP:0000035" + ], + "anomaly of the testis": [ + "HP:0000035" + ], + "anomaly of the testes": [ + "HP:0000035" + ], + "abnormal penis morphology": [ + "HP:0000036" + ], + "abnormality of the penis": [ + "HP:0000036" + ], + "male pseudohermaphroditism": [ + "HP:0000037" + ], + "epispadias": [ + "HP:0000039" + ], + "long penis": [ + "HP:0000040" + ], + "enlarge penis": [ + "HP:0000040" + ], + "enlarged penis": [ + "HP:0000040" + ], + "chordee": [ + "HP:0000041" + ], + "absent external genitalia": [ + "HP:0000042" + ], + "hypogonadotropic hypogonadism": [ + "HP:0000044" + ], + "hypogonadotrophic hypogonadism": [ + "HP:0000044" + ], + "isolated hypogonadotropic hypogonadism": [ + "HP:0000044" + ], + "low gonadotropin ( secondary hypogonadism )": [ + "HP:0000044" + ], + "low gonadotropins ( secondary hypogonadism )": [ + "HP:0000044" + ], + "abnormality of the scrotum": [ + "HP:0000045" + ], + "scrotal hypoplasia": [ + "HP:0000046" + ], + "hypoplastic scrotum": [ + "HP:0000046" + ], + "small than typical growth of scrotum": [ + "HP:0000046" + ], + "smaller than typical growth of scrotum": [ + "HP:0000046" + ], + "hypospadias": [ + "HP:0000047" + ], + "hypospadia": [ + "HP:0000047" + ], + "bifid scrotum": [ + "HP:0000048" + ], + "cleft of scrotum": [ + "HP:0000048" + ], + "scrotal cleft": [ + "HP:0000048" + ], + "shawl scrotum": [ + "HP:0000049" + ], + "override scrotum": [ + "HP:0000049" + ], + "overriding scrotum": [ + "HP:0000049" + ], + "scrotum surround penis": [ + "HP:0000049" + ], + "scrotum surrounds penis": [ + "HP:0000049" + ], + "hypoplastic male external genitalia": [ + "HP:0000050" + ], + "hypoplastic male genitalia": [ + "HP:0000050" + ], + "small male external genitalia": [ + "HP:0000050" + ], + "underdeveloped male genitalia": [ + "HP:0000050" + ], + "perineal hypospadias": [ + "HP:0000051" + ], + "urethral atresia , male": [ + "HP:0000052" + ], + "macroorchidism": [ + "HP:0000053" + ], + "large testicle": [ + "HP:0000053" + ], + "large testicles": [ + "HP:0000053" + ], + "large testis": [ + "HP:0000053" + ], + "micropenis": [ + "HP:0000054" + ], + "short penis": [ + "HP:0000054" + ], + "small penis": [ + "HP:0000054" + ], + "abnormality of female external genitalia": [ + "HP:0000055" + ], + "abnormal female external genitalia": [ + "HP:0000055" + ], + "abnormality of the clitoris": [ + "HP:0000056" + ], + "abnormality of the clit": [ + "HP:0000056" + ], + "obsolete clitoromegaly": [ + "HP:0000057" + ], + "abnormal labium morphology": [ + "HP:0000058" + ], + "abnormal labia morphology": [ + "HP:0000058" + ], + "abnormality of the labium": [ + "HP:0000058" + ], + "abnormality of the labia": [ + "HP:0000058" + ], + "hypoplastic labium majora": [ + "HP:0000059" + ], + "hypoplastic labia majora": [ + "HP:0000059" + ], + "hypoplasia of labium majora": [ + "HP:0000059" + ], + "hypoplasia of labia majora": [ + "HP:0000059" + ], + "small labium majora": [ + "HP:0000059" + ], + "small labia majora": [ + "HP:0000059" + ], + "underdeveloped vaginal lip": [ + "HP:0000059" + ], + "underdeveloped vaginal lips": [ + "HP:0000059" + ], + "clitoral hypoplasia": [ + "HP:0000060" + ], + "hypoplastic clitoris": [ + "HP:0000060" + ], + "small clitoris": [ + "HP:0000060" + ], + "underdeveloped clit": [ + "HP:0000060" + ], + "ambiguous genitalia , female": [ + "HP:0000061" + ], + "ambiguous genitalia due to virilization": [ + "HP:0000061" + ], + "atypical appearance of female genitals": [ + "HP:0000061" + ], + "ambiguous genitalia": [ + "HP:0000062" + ], + "ambiguous external genitalia": [ + "HP:0000062" + ], + "ambiguous external genitalia at birth": [ + "HP:0000062" + ], + "intersex genitalia": [ + "HP:0000062" + ], + "fuse labium minora": [ + "HP:0000063" + ], + "fused labia minora": [ + "HP:0000063" + ], + "fused inner lip": [ + "HP:0000063" + ], + "fused inner lips": [ + "HP:0000063" + ], + "hypoplastic labium minora": [ + "HP:0000064" + ], + "hypoplastic labia minora": [ + "HP:0000064" + ], + "underdeveloped inner lip": [ + "HP:0000064" + ], + "underdeveloped inner lips": [ + "HP:0000064" + ], + "labial hypertrophy": [ + "HP:0000065" + ], + "enlarge vaginal lip": [ + "HP:0000065" + ], + "enlarged vaginal lips": [ + "HP:0000065" + ], + "enlargement of the labium": [ + "HP:0000065" + ], + "enlargement of the labia": [ + "HP:0000065" + ], + "enlargement of the vaginal lip": [ + "HP:0000065" + ], + "enlargement of the vaginal lips": [ + "HP:0000065" + ], + "labial hypoplasia": [ + "HP:0000066" + ], + "hypoplastic labium": [ + "HP:0000066" + ], + "hypoplastic labia": [ + "HP:0000066" + ], + "underdeveloped labium": [ + "HP:0000066" + ], + "underdeveloped labia": [ + "HP:0000066" + ], + "urethral atresia , female": [ + "HP:0000067" + ], + "urethral atresia": [ + "HP:0000068" + ], + "absent urethral opening": [ + "HP:0000068" + ], + "urethral opening absent": [ + "HP:0000068" + ], + "abnormality of the ureter": [ + "HP:0000069" + ], + "abnormality of the ureters": [ + "HP:0000069" + ], + "ureter issue": [ + "HP:0000069" + ], + "ureteral anomaly": [ + "HP:0000069" + ], + "ureteral anomalies": [ + "HP:0000069" + ], + "ureterocele": [ + "HP:0000070" + ], + "ureteral stenosis": [ + "HP:0000071" + ], + "narrowing of the ureter": [ + "HP:0000071" + ], + "hydroureter": [ + "HP:0000072" + ], + "dilate ureter": [ + "HP:0000072" + ], + "dilated ureter": [ + "HP:0000072" + ], + "megaureter": [ + "HP:0000072" + ], + "swell of ureter": [ + "HP:0000072" + ], + "swelling of ureter": [ + "HP:0000072" + ], + "ureteral dilatation": [ + "HP:0000072" + ], + "uroureter": [ + "HP:0000072" + ], + "wide ureter": [ + "HP:0000072" + ], + "ureteral duplication": [ + "HP:0000073" + ], + "double ureter": [ + "HP:0000073" + ], + "ureteropelvic junction obstruction": [ + "HP:0000074" + ], + "pelviureteric junction obstruction": [ + "HP:0000074" + ], + "ureteropelvic junction stenosis": [ + "HP:0000074" + ], + "renal duplication": [ + "HP:0000075" + ], + "extra kidney": [ + "HP:0000075" + ], + "supernumerary kidney": [ + "HP:0000075" + ], + "vesicoureteral reflux": [ + "HP:0000076" + ], + "ureteral reflux": [ + "HP:0000076" + ], + "ureteric reflux": [ + "HP:0000076" + ], + "vesico - ureteral reflux": [ + "HP:0000076" + ], + "vesicoureteric reflux": [ + "HP:0000076" + ], + "abnormality of the kidney": [ + "HP:0000077" + ], + "abnormal kidney": [ + "HP:0000077" + ], + "renal anomaly": [ + "HP:0000077" + ], + "renal anomalies": [ + "HP:0000077" + ], + "abnormality of the genital system": [ + "HP:0000078" + ], + "abnormality of the reproductive system": [ + "HP:0000078" + ], + "genital abnormality": [ + "HP:0000078" + ], + "genital abnormalities": [ + "HP:0000078" + ], + "genital anomaly": [ + "HP:0000078" + ], + "genital anomalies": [ + "HP:0000078" + ], + "genital defect": [ + "HP:0000078" + ], + "genital defects": [ + "HP:0000078" + ], + "abnormality of the urinary system": [ + "HP:0000079" + ], + "urinary tract abnormality": [ + "HP:0000079" + ], + "urinary tract abnormalities": [ + "HP:0000079" + ], + "urinary tract anomaly": [ + "HP:0000079" + ], + "urinary tract anomalies": [ + "HP:0000079" + ], + "abnormality of reproductive system physiology": [ + "HP:0000080" + ], + "abnormality of genital physiology": [ + "HP:0000080" + ], + "genital functional abnormality": [ + "HP:0000080" + ], + "duplicate collecting system": [ + "HP:0000081" + ], + "duplicated collecting system": [ + "HP:0000081" + ], + "double collect system": [ + "HP:0000081" + ], + "double collecting system": [ + "HP:0000081" + ], + "double urinary collect system on intravenous pyelography": [ + "HP:0000081" + ], + "double urinary collecting systems on intravenous pyelography": [ + "HP:0000081" + ], + "duplex collect system": [ + "HP:0000081" + ], + "duplex collecting system": [ + "HP:0000081" + ], + "duplicate renal collecting system": [ + "HP:0000081" + ], + "duplicated renal collecting system": [ + "HP:0000081" + ], + "renal insufficiency": [ + "HP:0000083" + ], + "renal failure": [ + "HP:0000083" + ], + "renal failure in adulthood": [ + "HP:0000083" + ], + "horseshoe kidney": [ + "HP:0000085" + ], + "fuse kidney": [ + "HP:0000085" + ], + "fused kidneys": [ + "HP:0000085" + ], + "horseshoe kidneys": [ + "HP:0000085" + ], + "ectopic kidney": [ + "HP:0000086" + ], + "abnormal kidney location": [ + "HP:0000086" + ], + "displace kidney": [ + "HP:0000086" + ], + "displaced kidney": [ + "HP:0000086" + ], + "ectopic kidneys": [ + "HP:0000086" + ], + "renal ectopia": [ + "HP:0000086" + ], + "renal hypoplasia": [ + "HP:0000089" + ], + "hypoplastic kidney": [ + "HP:0000089" + ], + "hypoplastic kidneys": [ + "HP:0000089" + ], + "small kidney": [ + "HP:0000089" + ], + "small kidneys": [ + "HP:0000089" + ], + "underdeveloped kidney": [ + "HP:0000089" + ], + "underdeveloped kidneys": [ + "HP:0000089" + ], + "nephronophthisis": [ + "HP:0000090" + ], + "juvenile nephronophthisis": [ + "HP:0000090" + ], + "abnormal renal tubule morphology": [ + "HP:0000091" + ], + "abnormality of the renal tubule": [ + "HP:0000091" + ], + "morphologic abnormality of the renal tubule": [ + "HP:0000091" + ], + "morphologic abnormality of the renal tubules": [ + "HP:0000091" + ], + "renal tubular atrophy": [ + "HP:0000092" + ], + "renal tubular cell atrophy": [ + "HP:0000092" + ], + "tubular atrophy": [ + "HP:0000092" + ], + "proteinuria": [ + "HP:0000093" + ], + "high urine protein level": [ + "HP:0000093" + ], + "high urine protein levels": [ + "HP:0000093" + ], + "protein in urine": [ + "HP:0000093" + ], + "abnormal renal glomerulus morphology": [ + "HP:0000095" + ], + "abnormality of renal glomerulus morphology": [ + "HP:0000095" + ], + "morphologic abnormality of the renal glomerulus": [ + "HP:0000095" + ], + "glomerular sclerosis": [ + "HP:0000096" + ], + "glomerulosclerosis": [ + "HP:0000096" + ], + "renal glomerular fibrosis": [ + "HP:0000096" + ], + "focal segmental glomerulosclerosis": [ + "HP:0000097" + ], + "focal and segmental glomerular sclerosis": [ + "HP:0000097" + ], + "focal and segmental glomerulosclerosis": [ + "HP:0000097" + ], + "focal glomerulosclerosis": [ + "HP:0000097" + ], + "tall stature": [ + "HP:0000098" + ], + "accelerate linear growth": [ + "HP:0000098" + ], + "accelerated linear growth": [ + "HP:0000098" + ], + "increase body height": [ + "HP:0000098" + ], + "increased body height": [ + "HP:0000098" + ], + "increase linear growth": [ + "HP:0000098" + ], + "increased linear growth": [ + "HP:0000098" + ], + "glomerulonephritis": [ + "HP:0000099" + ], + "glomerular nephritis": [ + "HP:0000099" + ], + "nephrotic syndrome": [ + "HP:0000100" + ], + "nephrosis": [ + "HP:0000100" + ], + "polyuria": [ + "HP:0000103" + ], + "increase urine output": [ + "HP:0000103" + ], + "increased urine output": [ + "HP:0000103" + ], + "renal agenesis": [ + "HP:0000104" + ], + "absent kidney": [ + "HP:0000104" + ], + "miss kidney": [ + "HP:0000104" + ], + "missing kidney": [ + "HP:0000104" + ], + "renal aplasia": [ + "HP:0000104" + ], + "enlarge kidney": [ + "HP:0000105" + ], + "enlarged kidney": [ + "HP:0000105" + ], + "large kidney": [ + "HP:0000105" + ], + "large kidneys": [ + "HP:0000105" + ], + "nephromegaly": [ + "HP:0000105" + ], + "renal enlargement": [ + "HP:0000105" + ], + "renal cyst": [ + "HP:0000107" + ], + "cystic kidney disease": [ + "HP:0000107" + ], + "cystic kidney": [ + "HP:0000107" + ], + "cystic kidneys": [ + "HP:0000107" + ], + "kidney cyst": [ + "HP:0000107" + ], + "renal cysts": [ + "HP:0000107" + ], + "renal corticomedullary cyst": [ + "HP:0000108" + ], + "renal corticomedullary cysts": [ + "HP:0000108" + ], + "corticomedullary renal cyst": [ + "HP:0000108" + ], + "corticomedullary renal cysts": [ + "HP:0000108" + ], + "renal corticomedullary cystic disease": [ + "HP:0000108" + ], + "renal dysplasia": [ + "HP:0000110" + ], + "dysplastic kidney": [ + "HP:0000110" + ], + "dysplastic kidneys": [ + "HP:0000110" + ], + "renal adysplasia": [ + "HP:0000110" + ], + "renal juxtaglomerular cell hypertrophy / hyperplasia": [ + "HP:0000111" + ], + "nephropathy": [ + "HP:0000112" + ], + "kidney damage": [ + "HP:0000112" + ], + "kidney disease": [ + "HP:0000112" + ], + "polycystic kidney dysplasia": [ + "HP:0000113" + ], + "enlarge polycystic kidney": [ + "HP:0000113" + ], + "enlarged polycystic kidneys": [ + "HP:0000113" + ], + "polycystic kidney disease": [ + "HP:0000113" + ], + "polycystic kidney": [ + "HP:0000113" + ], + "polycystic kidneys": [ + "HP:0000113" + ], + "proximal tubulopathy": [ + "HP:0000114" + ], + "proximal renal tubule defect": [ + "HP:0000114" + ], + "proximal renal tubulopathy": [ + "HP:0000114" + ], + "proximal tubular defect": [ + "HP:0000114" + ], + "proximal tubule dysfunction": [ + "HP:0000114" + ], + "selective proximal tubular damage": [ + "HP:0000114" + ], + "renal phosphate wasting": [ + "HP:0000117" + ], + "decrease renal tubular phosphate reabsorption": [ + "HP:0000117" + ], + "decreased renal tubular phosphate reabsorption": [ + "HP:0000117" + ], + "decrease tubular maximum for phosphate reabsorption per glomerular filtration rate": [ + "HP:0000117" + ], + "decreased tubular maximum for phosphate reabsorption per glomerular filtration rate": [ + "HP:0000117" + ], + "tubular phosphate reabsorption low": [ + "HP:0000117" + ], + "phenotypic abnormality": [ + "HP:0000118" + ], + "organ abnormality": [ + "HP:0000118" + ], + "abnormality of the genitourinary system": [ + "HP:0000119" + ], + "abnormality of the gu system": [ + "HP:0000119" + ], + "genitourinary abnormality": [ + "HP:0000119" + ], + "genitourinary disease": [ + "HP:0000119" + ], + "genitourinary dysplasia": [ + "HP:0000119" + ], + "genitourinary tract anomaly": [ + "HP:0000119" + ], + "genitourinary tract anomalies": [ + "HP:0000119" + ], + "genitourinary tract malformation": [ + "HP:0000119" + ], + "urogenital abnormality": [ + "HP:0000119" + ], + "urogenital abnormalities": [ + "HP:0000119" + ], + "urogenital anomaly": [ + "HP:0000119" + ], + "urogenital anomalies": [ + "HP:0000119" + ], + "nephrocalcinosis": [ + "HP:0000121" + ], + "increased calcium level in kidney": [ + "HP:0000121" + ], + "too much calcium deposit in kidney": [ + "HP:0000121" + ], + "too much calcium deposited in kidneys": [ + "HP:0000121" + ], + "unilateral renal agenesis": [ + "HP:0000122" + ], + "absent kidney on one side": [ + "HP:0000122" + ], + "miss one kidney": [ + "HP:0000122" + ], + "missing one kidney": [ + "HP:0000122" + ], + "single kidney": [ + "HP:0000122" + ], + "unilateral kidney agenesis": [ + "HP:0000122" + ], + "nephritis": [ + "HP:0000123" + ], + "kidney inflammation": [ + "HP:0000123" + ], + "renal tubular dysfunction": [ + "HP:0000124" + ], + "abnormal function of filtrate structure in kidney": [ + "HP:0000124" + ], + "abnormal function of filtrating structures in kidney": [ + "HP:0000124" + ], + "renal tubular defect": [ + "HP:0000124" + ], + "renal tubular disease": [ + "HP:0000124" + ], + "pelvic kidney": [ + "HP:0000125" + ], + "sacral kidney": [ + "HP:0000125" + ], + "hydronephrosis": [ + "HP:0000126" + ], + "renal salt waste": [ + "HP:0000127" + ], + "renal salt wasting": [ + "HP:0000127" + ], + "loss of salt in urine": [ + "HP:0000127" + ], + "renal salt - wasting": [ + "HP:0000127" + ], + "salt waste": [ + "HP:0000127" + ], + "salt wasting": [ + "HP:0000127" + ], + "salt - wasting": [ + "HP:0000127" + ], + "renal potassium wasting": [ + "HP:0000128" + ], + "renal k waste": [ + "HP:0000128" + ], + "renal k wasting": [ + "HP:0000128" + ], + "abnormality of the uterus": [ + "HP:0000130" + ], + "uterine abnormality": [ + "HP:0000130" + ], + "uterine abnormalities": [ + "HP:0000130" + ], + "uterine malformation": [ + "HP:0000130" + ], + "uterine malformations": [ + "HP:0000130" + ], + "uterine leiomyoma": [ + "HP:0000131" + ], + "benign uterine leiomyoma": [ + "HP:0000131" + ], + "benign uterine leiomyomas": [ + "HP:0000131" + ], + "uterine fibroid": [ + "HP:0000131" + ], + "menorrhagia": [ + "HP:0000132" + ], + "abnormally heavy bleeding during menstruation": [ + "HP:0000132" + ], + "abnormally heavy period": [ + "HP:0000132" + ], + "abnormally heavy periods": [ + "HP:0000132" + ], + "hypermenorrhea": [ + "HP:0000132" + ], + "gonadal dysgenesis": [ + "HP:0000133" + ], + "mixed gonadal dysgenesis": [ + "HP:0000133" + ], + "pure gonadal dysgenesis": [ + "HP:0000133" + ], + "female hypogonadism": [ + "HP:0000134" + ], + "hypogonadism , female": [ + "HP:0000134" + ], + "hypogonadism": [ + "HP:0000135" + ], + "decreased activity of gonad": [ + "HP:0000135" + ], + "decreased activity of gonads": [ + "HP:0000135" + ], + "bifid uterus": [ + "HP:0000136" + ], + "abnormality of the ovary": [ + "HP:0000137" + ], + "abnormality of the ovaries": [ + "HP:0000137" + ], + "ovarian disease": [ + "HP:0000137" + ], + "ovarian cyst": [ + "HP:0000138" + ], + "cystic abnormality of the ovary": [ + "HP:0000138" + ], + "cystic abnormalities of the ovaries": [ + "HP:0000138" + ], + "cystic ovary": [ + "HP:0000138" + ], + "cystic ovaries": [ + "HP:0000138" + ], + "ovarian cystic abnormality": [ + "HP:0000138" + ], + "uterine prolapse": [ + "HP:0000139" + ], + "sag uterus": [ + "HP:0000139" + ], + "sagging uterus": [ + "HP:0000139" + ], + "abnormality of the menstrual cycle": [ + "HP:0000140" + ], + "menstrual abnormality": [ + "HP:0000140" + ], + "menstrual abnormalities": [ + "HP:0000140" + ], + "amenorrhea": [ + "HP:0000141" + ], + "abnormal absence of menstruation": [ + "HP:0000141" + ], + "abnormal vagina morphology": [ + "HP:0000142" + ], + "vaginal malformation": [ + "HP:0000142" + ], + "rectovaginal fistula": [ + "HP:0000143" + ], + "abnormal connection between rectum and vagina": [ + "HP:0000143" + ], + "decrease fertility": [ + "HP:0000144" + ], + "decreased fertility": [ + "HP:0000144" + ], + "abnormal fertility": [ + "HP:0000144" + ], + "transverse vaginal septum": [ + "HP:0000145" + ], + "transverse vaginal membrane": [ + "HP:0000145" + ], + "polycystic ovary": [ + "HP:0000147" + ], + "polycystic ovaries": [ + "HP:0000147" + ], + "polycystic ovary disease": [ + "HP:0000147" + ], + "sclerocystic ovary": [ + "HP:0000147" + ], + "sclerocystic ovaries": [ + "HP:0000147" + ], + "vaginal atresia": [ + "HP:0000148" + ], + "abnormally close or absent vagina": [ + "HP:0000148" + ], + "abnormally closed or absent vagina": [ + "HP:0000148" + ], + "ovarian 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mouth": [ + "HP:0000160" + ], + "small oral aperture": [ + "HP:0000160" + ], + "median cleft lip": [ + "HP:0000161" + ], + "central cleft upper lip": [ + "HP:0000161" + ], + "midline cleft lip": [ + "HP:0000161" + ], + "glossoptosis": [ + "HP:0000162" + ], + "lingual retraction": [ + "HP:0000162" + ], + "posterior displacement of the tongue": [ + "HP:0000162" + ], + "retraction of the tongue": [ + "HP:0000162" + ], + "abnormal oral cavity morphology": [ + "HP:0000163" + ], + "abnormality of the oral cavity": [ + "HP:0000163" + ], + "abnormality of the dentition": [ + "HP:0000164" + ], + "abnormal dentition": [ + "HP:0000164" + ], + "abnormal teeth": [ + "HP:0000164" + ], + "abnormality of the teeth": [ + "HP:0000164" + ], + "dental abnormality": [ + "HP:0000164" + ], + "dental abnormalities": [ + "HP:0000164" + ], + "dental anomaly": [ + "HP:0000164" + ], + "dental anomalies": [ + "HP:0000164" + ], + "dental problem": [ + "HP:0000164" + ], + "dental problems": [ + "HP:0000164" + ], + 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closing fontanelles": [ + "HP:0000270" + ], + "late closure of fontanelle": [ + "HP:0000270" + ], + "late - closing fontanelle": [ + "HP:0000270" + ], + "open suture": [ + "HP:0000270" + ], + "open sutures": [ + "HP:0000270" + ], + "abnormality of the face": [ + "HP:0000271" + ], + "abnormal face": [ + "HP:0000271" + ], + "abnormality of the countenance": [ + "HP:0000271" + ], + "abnormality of the physiognomy": [ + "HP:0000271" + ], + "abnormality of the visage": [ + "HP:0000271" + ], + "anomaly of face": [ + "HP:0000271" + ], + "anomaly of the face": [ + "HP:0000271" + ], + "disorder of face": [ + "HP:0000271" + ], + "disorder of the face": [ + "HP:0000271" + ], + "facial abnormality": [ + "HP:0000271" + ], + "facial anomaly": [ + "HP:0000271" + ], + "malar flattening": [ + "HP:0000272" + ], + "decreased size of malar bone": [ + "HP:0000272" + ], + "depressed malar region": [ + "HP:0000272" + ], + "flat cheekbone": [ + "HP:0000272" + ], + "hypotrophic malar bone": [ + "HP:0000272" + 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[ + "HP:0000298" + ], + "expressionless face": [ + "HP:0000298" + ], + "lack of facial expression": [ + "HP:0000298" + ], + "mask - like facial appearance": [ + "HP:0000298" + ], + "masklike facies": [ + "HP:0000298" + ], + "oval face": [ + "HP:0000300" + ], + "oval facial shape": [ + "HP:0000300" + ], + "oval facies": [ + "HP:0000300" + ], + "abnormality of facial musculature": [ + "HP:0000301" + ], + "abnormality of facial muscle": [ + "HP:0000301" + ], + "abnormality of facial muscles": [ + "HP:0000301" + ], + "facial muscle issue": [ + "HP:0000301" + ], + "mandibular prognathia": [ + "HP:0000303" + ], + "big low jaw": [ + "HP:0000303" + ], + "big lower jaw": [ + "HP:0000303" + ], + "big mandible": [ + "HP:0000303" + ], + "enlarge mandible": [ + "HP:0000303" + ], + "enlarged mandible": [ + "HP:0000303" + ], + "enlargement of mandible": [ + "HP:0000303" + ], + "hyperplasia of low jaw": [ + "HP:0000303" + ], + "hyperplasia of lower jaw": [ + "HP:0000303" + ], + "hypertrophy of low 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excess": [ + "HP:0000303" + ], + "mandibular hyperplasia": [ + "HP:0000303" + ], + "mandibular macrognathia": [ + "HP:0000303" + ], + "mandibular prognathism": [ + "HP:0000303" + ], + "prognathia": [ + "HP:0000303" + ], + "prognathism": [ + "HP:0000303" + ], + "prominent chin": [ + "HP:0000303" + ], + "prominent jaw": [ + "HP:0000303" + ], + "prominent low jaw": [ + "HP:0000303" + ], + "prominent lower jaw": [ + "HP:0000303" + ], + "prominent mandible": [ + "HP:0000303" + ], + "relative mandibular prognathism": [ + "HP:0000303" + ], + "abnormality of the chin": [ + "HP:0000306" + ], + "abnormality of the menton": [ + "HP:0000306" + ], + "anomaly of the chin": [ + "HP:0000306" + ], + "deformity of the chin": [ + "HP:0000306" + ], + "malformation of the chin": [ + "HP:0000306" + ], + "point chin": [ + "HP:0000307" + ], + "pointed chin": [ + "HP:0000307" + ], + "point mention region": [ + "HP:0000307" + ], + "pointed mention region": [ + "HP:0000307" + ], + "pointy chin": [ + "HP:0000307" + ], + "small point chin": [ + "HP:0000307" + ], + "small pointed chin": [ + "HP:0000307" + ], + "witch 's chin": [ + "HP:0000307" + ], + "microretrognathia": [ + "HP:0000308" + ], + "retromicrognathia": [ + "HP:0000308" + ], + "small retruded chin": [ + "HP:0000308" + ], + "abnormality of the midface": [ + "HP:0000309" + ], + "anomaly of the midface": [ + "HP:0000309" + ], + "deformity of the midface": [ + "HP:0000309" + ], + "malformation of the midface": [ + "HP:0000309" + ], + "round face": [ + "HP:0000311" + ], + "circular face": [ + "HP:0000311" + ], + "round facial appearance": [ + "HP:0000311" + ], + "round facial shape": [ + "HP:0000311" + ], + "round facies": [ + "HP:0000311" + ], + "round , full face": [ + "HP:0000311" + ], + "abnormality of the orbital region": [ + "HP:0000315" + ], + "abnormality of the eye region": [ + "HP:0000315" + ], + "abnormality of the region around the eye": [ + "HP:0000315", + "HP:0000606" + ], + "abnormality of the region around the eyes": [ + "HP:0000315" + ], + "anomaly of the orbital region of the face": [ + "HP:0000315" + ], + "deformity of the orbital region of the face": [ + "HP:0000315" + ], + "malformation of the orbital region of the face": [ + "HP:0000315" + ], + "hypertelorism": [ + "HP:0000316" + ], + "excessive orbital separation": [ + "HP:0000316" + ], + "increase distance between eye socket": [ + "HP:0000316" + ], + "increased distance between eye sockets": [ + "HP:0000316" + ], + "increase distance between eye": [ + "HP:0000316" + ], + "increased distance between eyes": [ + "HP:0000316" + ], + "increase interpupillary distance": [ + "HP:0000316" + ], + "increased interpupillary distance": [ + "HP:0000316" + ], + "ocular hypertelorism": [ + "HP:0000316" + ], + "wide - set eye": [ + "HP:0000316" + ], + "wide - set eyes": [ + "HP:0000316" + ], + "widely space eye": [ + "HP:0000316" + ], + "widely spaced eyes": [ + "HP:0000316" + ], + "widen interpupillary distance": [ + "HP:0000316" + ], + "widened 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"abnormality of the maxilla": [ + "HP:0000326" + ], + "abnormality of the upper jaw bone": [ + "HP:0000326" + ], + "abnormality of the upper jaw bones": [ + "HP:0000326" + ], + "anomaly of the maxilla": [ + "HP:0000326" + ], + "deformity of the maxilla": [ + "HP:0000326" + ], + "deformity of the upper jaw bone": [ + "HP:0000326" + ], + "deformity of the upper jaw bones": [ + "HP:0000326" + ], + "malformation of the maxilla": [ + "HP:0000326" + ], + "malformation of the upper jaw bone": [ + "HP:0000326" + ], + "malformation of the upper jaw bones": [ + "HP:0000326" + ], + "hypoplasia of the maxilla": [ + "HP:0000327" + ], + "decreased projection of maxilla": [ + "HP:0000327" + ], + "decreased projection of upper jaw": [ + "HP:0000327" + ], + "decreased size of maxilla": [ + "HP:0000327" + ], + "decreased size of upper jaw": [ + "HP:0000327" + ], + "deficiency of upper jaw bone": [ + "HP:0000327" + ], + "deficiency of upper jaw bones": [ + "HP:0000327" + ], + "hypoplasia of upper jaw bone": [ + "HP:0000327" + ], + "hypoplasia of upper jaw bones": [ + "HP:0000327" + ], + "hypoplastic maxillary bone": [ + "HP:0000327" + ], + "hypoplastic maxillary bones": [ + "HP:0000327" + ], + "hypotrophic maxilla": [ + "HP:0000327" + ], + "hypotrophic upper jaw bone": [ + "HP:0000327" + ], + "hypotrophic upper jaw bones": [ + "HP:0000327" + ], + "maxillary deficiency": [ + "HP:0000327" + ], + "maxillary hypoplasia": [ + "HP:0000327" + ], + "maxillary micrognathia": [ + "HP:0000327" + ], + "maxillary retrognathia": [ + "HP:0000327" + ], + "maxillary retrusion": [ + "HP:0000327" + ], + "micromaxilla": [ + "HP:0000327" + ], + "retrognathia of upper jaw": [ + "HP:0000327" + ], + "retrusion of upper jaw bone": [ + "HP:0000327" + ], + "retrusion of upper jaw bones": [ + "HP:0000327" + ], + "small maxilla": [ + "HP:0000327" + ], + "small upper jaw": [ + "HP:0000327" + ], + "small upper jaw bone": [ + "HP:0000327" + ], + "small upper jaw bones": [ + "HP:0000327" + ], + "upper jaw deficiency": [ + "HP:0000327" + ], + "upper jaw retrusion": [ + "HP:0000327" + ], + "facial hemangioma": [ + "HP:0000329" + ], + "facial hemangiomata": [ + "HP:0000329" + ], + "short chin": [ + "HP:0000331" + ], + "decreased height of chin": [ + "HP:0000331" + ], + "short low third of face": [ + "HP:0000331" + ], + "short lower third of face": [ + "HP:0000331" + ], + "small chin": [ + "HP:0000331" + ], + "vertical deficiency of chin": [ + "HP:0000331" + ], + "vertical hypoplasia of chin": [ + "HP:0000331" + ], + "prominent supraorbital ridge": [ + "HP:0000336" + ], + "prominent supraorbital ridges": [ + "HP:0000336" + ], + "hyperplasia of supraorbital margin": [ + "HP:0000336" + ], + "hyperplasia of supraorbital margins": [ + "HP:0000336" + ], + "hyperplasia of supraorbital ridge": [ + "HP:0000336" + ], + "hypertrophy of supraorbital margin": [ + "HP:0000336" + ], + "hypertrophy of supraorbital margins": [ + "HP:0000336" + ], + "hypertrophy of supraorbital ridge": [ + "HP:0000336" + ], 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"decrease facial muscle movement": [ + "HP:0000338" + ], + "decreased facial muscle movement": [ + "HP:0000338" + ], + "dull facial expression": [ + "HP:0000338" + ], + "hypomimia": [ + "HP:0000338" + ], + "pugilistic facies": [ + "HP:0000339" + ], + "boxer - like facial appearance": [ + "HP:0000339" + ], + "pugilistic facial appearance": [ + "HP:0000339" + ], + "slop forehead": [ + "HP:0000340" + ], + "sloping forehead": [ + "HP:0000340" + ], + "incline forehead": [ + "HP:0000340" + ], + "inclined forehead": [ + "HP:0000340" + ], + "posteriorly slop forehead": [ + "HP:0000340" + ], + "posteriorly sloping forehead": [ + "HP:0000340" + ], + "recede forehead": [ + "HP:0000340" + ], + "receding forehead": [ + "HP:0000340" + ], + "narrow forehead": [ + "HP:0000341" + ], + "bitemporal narrowing": [ + "HP:0000341" + ], + "bitemporal narrowness": [ + "HP:0000341" + ], + "bitemporal skull narrowing": [ + "HP:0000341" + ], + "decrease width of the forehead": [ + "HP:0000341" + ], + "decreased width of the forehead": [ + "HP:0000341" + ], + "intertemporal narrowing": [ + "HP:0000341" + ], + "narrow bitemporal diameter": [ + "HP:0000341" + ], + "narrow bitemporal width": [ + "HP:0000341" + ], + "temporal narrowness": [ + "HP:0000341" + ], + "long philtrum": [ + "HP:0000343" + ], + "elongate philtrum": [ + "HP:0000343" + ], + "elongated philtrum": [ + "HP:0000343" + ], + "increase height of philtrum": [ + "HP:0000343" + ], + "increased height of philtrum": [ + "HP:0000343" + ], + "increased length of philtrum": [ + "HP:0000343" + ], + "increased vertical dimension of philtrum": [ + "HP:0000343" + ], + "vertical hyperplasia of philtrum": [ + "HP:0000343" + ], + "whistle appearance": [ + "HP:0000346" + ], + "whistling appearance": [ + "HP:0000346" + ], + "whistle facial appearance": [ + "HP:0000346" + ], + "whistling facial appearance": [ + "HP:0000346" + ], + "micrognathia": [ + "HP:0000347" + ], + "decreased projection of low jaw": [ + "HP:0000347" + ], + "decreased projection of lower jaw": [ + "HP:0000347" + ], + "decreased projection of mandible": [ + "HP:0000347" + ], + "decreased size of low jaw": [ + "HP:0000347" + ], + "decreased size of lower jaw": [ + "HP:0000347" + ], + "decreased size of mandible": [ + "HP:0000347" + ], + "deficiency of low jaw": [ + "HP:0000347" + ], + "deficiency of lower jaw": [ + "HP:0000347" + ], + "hypoplasia of low jaw": [ + "HP:0000347" + ], + "hypoplasia of lower jaw": [ + "HP:0000347" + ], + "hypoplasia of mandible": [ + "HP:0000347" + ], + "hypoplastic mandible": [ + "HP:0000347" + ], + "hypoplastic mandible condyle": [ + "HP:0000347" + ], + "hypotrophic low jaw": [ + "HP:0000347" + ], + "hypotrophic lower jaw": [ + "HP:0000347" + ], + "hypotrophic mandible": [ + "HP:0000347" + ], + "little low jaw": [ + "HP:0000347" + ], + "little lower jaw": [ + "HP:0000347" + ], + "little mandible": [ + "HP:0000347" + ], + "low jaw deficiency": [ + "HP:0000347" + ], + "lower jaw deficiency": [ + "HP:0000347" + ], + "low jaw hypoplasia": [ + "HP:0000347" + ], + "lower jaw hypoplasia": [ + "HP:0000347" + ], + "low jaw retrusion": [ + "HP:0000347" + ], + "lower jaw retrusion": [ + "HP:0000347" + ], + "mandibular deficiency": [ + "HP:0000347" + ], + "mandibular hypoplasia": [ + "HP:0000347" + ], + "mandibular micrognathia": [ + "HP:0000347" + ], + "mandibular retrognathia": [ + "HP:0000347" + ], + "mandibular retrusion": [ + "HP:0000347" + ], + "micrognathia of low jaw": [ + "HP:0000347" + ], + "micrognathia of lower jaw": [ + "HP:0000347" + ], + "micromandible": [ + "HP:0000347" + ], + "retrusion of low jaw": [ + "HP:0000347" + ], + "retrusion of lower jaw": [ + "HP:0000347" + ], + "robin mandible": [ + "HP:0000347" + ], + "severe hypoplasia of mandible": [ + "HP:0000347" + ], + "small jaw": [ + "HP:0000347" + ], + "small low jaw": [ + "HP:0000347" + ], + "small lower jaw": [ + "HP:0000347" + ], + "small mandible": [ + "HP:0000347" + ], + "underdevelopment of low jaw": [ + "HP:0000347" + ], + "underdevelopment of lower jaw": [ + "HP:0000347" + ], + "underdevelopment of mandible": [ + "HP:0000347" + ], + "high forehead": [ + "HP:0000348" + ], + "tall forehead": [ + "HP:0000348" + ], + "widow 's peak": [ + "HP:0000349" + ], + "hairline peak": [ + "HP:0000349" + ], + "hairline point": [ + "HP:0000349" + ], + "point frontal hairline": [ + "HP:0000349" + ], + "pointed frontal hairline": [ + "HP:0000349" + ], + "point hairline at front of head": [ + "HP:0000349" + ], + "pointed hairline at front of head": [ + "HP:0000349" + ], + "v - shaped frontal hairline": [ + "HP:0000349" + ], + "small forehead": [ + "HP:0000350" + ], + "decreased size of forehead": [ + "HP:0000350" + ], + "decreased size of frontal region of face": [ + "HP:0000350" + ], + "hypoplasia of forehead": [ + "HP:0000350" + ], + "hypotrophic forehead": [ + "HP:0000350" + ], + "abnormality of the outer ear": [ + "HP:0000356" + ], + "abnormal pinna": [ + "HP:0000356" + ], + "abnormal pinnae": [ + "HP:0000356" + ], + "abnormality of the auricle": [ + "HP:0000356" + ], + "abnormality of the external ear": [ + "HP:0000356" + ], + "ear anomaly": [ + "HP:0000356", + "HP:0000598" + ], + "ear anomalies": [ + "HP:0000356" + ], + "external ear malformation": [ + "HP:0008572" + ], + "external ear malformations": [ + "HP:0000356" + ], + "malformed pinna": [ + "HP:0000356" + ], + "malformed pinnae": [ + "HP:0000356" + ], + "outer ear abnormality": [ + "HP:0000356" + ], + "abnormal location of ear": [ + "HP:0000357" + ], + "abnormal location of ears": [ + "HP:0000357" + ], + "external ear position defect": [ + "HP:0000357" + ], + "posteriorly rotate ear": [ + "HP:0000358" + ], + "posteriorly rotated ears": [ + "HP:0000358" + ], + "ear , posterior angulation , increase": [ + "HP:0000358" + ], + "ear , posterior angulation , increased": [ + "HP:0000358" + ], + "ear rotate toward back of head": [ + "HP:0000358" + ], + "ears rotated toward back of head": [ + "HP:0000358" + ], + "posteriorly angulate ear": [ + "HP:0000358" + ], + "posteriorly angulated ears": [ + "HP:0000358" + ], + "posteriorly rotate": [ + "HP:0000358" + ], + "posteriorly rotated": [ + "HP:0000358" + ], + "posteriorly rotate auricle": [ + "HP:0000358" + ], + "posteriorly rotated auricles": [ + "HP:0000358" + ], + "posteriorly - angulated ear": [ + "HP:0000358" + ], + "posteriorly - angulated ears": [ + "HP:0000358" + ], + "posteriorly - rotate ear": [ + "HP:0000358" + ], + "posteriorly - rotated ears": [ + "HP:0000358" + ], + "abnormality of the inner ear": [ + "HP:0000359" + ], + "inner ear abnormality": [ + "HP:0000359" + ], + "tinnitus": [ + "HP:0000360" + ], + "ring in ear": [ + "HP:0000360" + ], + "ringing in ears": [ + "HP:0000360" + ], + "ring in the ear": [ + "HP:0000360" + ], + "ringing in the ears": [ + "HP:0000360" + ], + "obsolete pulsatile tinnitus ( tympanic paraganglioma )": [ + "HP:0000361" + ], + "otosclerosis": [ + "HP:0000362" + ], + "abnormality of earlobe": [ + "HP:0000363" + ], + "abnormal earlobe": [ 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+ "low - set , posteriorly rotate ear": [ + "HP:0000368" + ], + "low - set , posteriorly rotated ears": [ + "HP:0000368" + ], + "low - set posteriorly rotated ear": [ + "HP:0000368" + ], + "low - set posteriorly rotated ears": [ + "HP:0000368" + ], + "low - set ear": [ + "HP:0000369" + ], + "low - set ears": [ + "HP:0000369" + ], + "low set ear": [ + "HP:0000369" + ], + "low set ears": [ + "HP:0000369" + ], + "low - set pinna": [ + "HP:0000369" + ], + "low - set pinnae": [ + "HP:0000369" + ], + "lowset ear": [ + "HP:0000369" + ], + "lowset ears": [ + "HP:0000369" + ], + "melotia": [ + "HP:0000369" + ], + "abnormality of the middle ear": [ + "HP:0000370" + ], + "middle ear abnormality": [ + "HP:0000370" + ], + "middle ear abnormalities": [ + "HP:0000370" + ], + "acute otitis medium": [ + "HP:0000371" + ], + "acute otitis media": [ + "HP:0000371" + ], + "acute middle ear infection": [ + "HP:0000371" + ], + "abnormality of the auditory canal": [ + "HP:0000372" + ], + "auditory canal abnormality": [ + "HP:0000372" + ], + "abnormal cochlea morphology": [ + "HP:0000375" + ], + "abnormality of cochlea": [ + "HP:0000375" + ], + "incomplete partition of the cochlea type ii": [ + "HP:0000376" + ], + "mondini malformation": [ + "HP:0000376" + ], + "abnormality of the pinna": [ + "HP:0000377" + ], + "abnormal form of ear": [ + "HP:0000377" + ], + "abnormal form of ears": [ + "HP:0000377" + ], + "abnormally shaped ear": [ + "HP:0000377" + ], + "abnormally shaped ears": [ + "HP:0000377" + ], + "auricular malformation": [ + "HP:0000377" + ], + "deform auricle": [ + "HP:0000377" + ], + "deformed auricles": [ + "HP:0000377" + ], + "deform ear": [ + "HP:0000377" + ], + "deformed ears": [ + "HP:0000377" + ], + "dysplastic ear": [ + "HP:0000377" + ], + "dysplastic ears": [ + "HP:0000377" + ], + "malformation of auricle": [ + "HP:0000377" + ], + "malformed auricle": [ + "HP:0000377" + ], + "malformed auricles": [ + "HP:0000377" + ], + "malformed ear": [ + "HP:0000377" + ], + "malformed ears": [ + "HP:0000377" + ], + "malformed external ear": [ + "HP:0000377" + ], + "malformed external ears": [ + "HP:0000377" + ], + "minor malformation of the auricle": [ + "HP:0000377" + ], + "minor malformation of the auricles": [ + "HP:0000377" + ], + "poorly define concha": [ + "HP:0000377" + ], + "poorly defined conchae": [ + "HP:0000377" + ], + "cup ear": [ + "HP:0000378" + ], + "cupped ear": [ + "HP:0000378" + ], + "capuchin ear": [ + "HP:0000378" + ], + "capuchin ears": [ + "HP:0000378" + ], + "cup - shaped ear": [ + "HP:0000378" + ], + "cup - shaped ears": [ + "HP:0000378" + ], + "cupped ears": [ + "HP:0000378" + ], + "simple , cup - shaped ear": [ + "HP:0000378" + ], + "simple , cup - shaped ears": [ + "HP:0000378" + ], + "stapes ankylosis": [ + "HP:0000381" + ], + "stapes fixation": [ + "HP:0000381" + ], + "abnormality of periauricular region": [ + "HP:0000383" + ], + "abnormality of the region around the ear": [ + "HP:0000383" + ], + "anomaly of the periauricular region": [ + "HP:0000383" + ], + "deformity of the periauricular region": [ + "HP:0000383" + ], + "malformation of the periauricular region": [ + "HP:0000383" + ], + "preauricular skin tag": [ + "HP:0000384" + ], + "ear tag": [ + "HP:0000384" + ], + "periauricular skin tag": [ + "HP:0000384" + ], + "preauricular acrochordon": [ + "HP:0000384" + ], + "preauricular fibroepithelial polyp": [ + "HP:0000384" + ], + "preauricular skin tags": [ + "HP:0000384" + ], + "preauricular tag": [ + "HP:0000384" + ], + "preauricular tags": [ + "HP:0000384" + ], + "skin tag in front of the ear": [ + "HP:0000384" + ], + "skin tag on the posterior cheek": [ + "HP:0000384" + ], + "small earlobe": [ + "HP:0000385" + ], + "hypoplastic earlobe": [ + "HP:0000385" + ], + "hypoplastic earlobes": [ + "HP:0000385" + ], + "hypoplastic lobule": [ + "HP:0000385" + ], + "hypoplastic lobules": [ + "HP:0000385" + ], + "small earlobes": [ + "HP:0000385" + ], + "absent earlobe": [ + "HP:0000387" + ], + "absent ear lobe": [ + "HP:0000387" + ], + "absent ear lobes": [ + "HP:0000387" + ], + "earlobe , absent": [ + "HP:0000387" + ], + "lobeless ear": [ + "HP:0000387" + ], + "lobeless ears": [ + "HP:0000387" + ], + "otitis medium": [ + "HP:0000388" + ], + "otitis media": [ + "HP:0000388" + ], + "middle ear infection": [ + "HP:0000388" + ], + "chronic otitis medium": [ + "HP:0000389" + ], + "chronic otitis media": [ + "HP:0000389" + ], + "chronic ear infection": [ + "HP:0000389" + ], + "chronic infection of the middle ear": [ + "HP:0000389" + ], + "chronic infections of the middle ear": [ + "HP:0000389" + ], + "chronic middle ear infection": [ + "HP:0000389" + ], + "otitis medium , chronic": [ + "HP:0000389" + ], + "otitis media , chronic": [ + "HP:0000389" + ], + "thicken helix": [ + "HP:0000391" + ], + "thickened helices": [ + "HP:0000391" + ], + "thick helix": [ + "HP:0000391" + ], + "lop ear": [ + "HP:0000394" + ], + "prominent antihelix": [ + "HP:0000395" + ], + "overfolded helix": [ + "HP:0000396" + ], + "over - folded helix": [ + "HP:0000396" + ], + "over - folded helices": [ + "HP:0000396" + ], + "overfolded ear": [ + "HP:0000396" + ], + "overfolded ears": [ + "HP:0000396" + ], + "overfolded helices": [ + "HP:0000396" + ], + "prelingual sensorineural hearing impairment": [ + "HP:0000399" + ], + "deafness , sensorineural , prelingual": [ + "HP:0000399" + ], + "prelingual sensorineural deafness": [ + "HP:0000399" + ], + "macrotia": [ + "HP:0000400" + ], + "large ear": [ + "HP:0000400" + ], + "large ears": [ + "HP:0000400" + ], + "large pinna": [ + "HP:0000400" + ], + "large pinnae": [ + "HP:0000400" + ], + "stenosis of the external auditory canal": [ + "HP:0000402" + ], + "external auditory canal stenosis": [ + "HP:0000402" + ], + "narrow auditory canal": [ + "HP:0000402" + ], + "narrow auditory canals": [ + "HP:0000402" + ], + "narrow ear canal": [ + "HP:0000402" + ], + "narrow external auditory canal": [ + "HP:0000402" + ], + "narrow external auditory canals": [ + "HP:0000402" + ], + "narrow external auditory meatus": [ + "HP:0000402" + ], + "narrowing of passageway from out ear to middle ear": [ + "HP:0000402" + ], + "narrowing of passageway from outer ear to middle ear": [ + "HP:0000402" + ], + "stenotic external auditory canal": [ + "HP:0000402" + ], + "recurrent otitis medium": [ + "HP:0000403" + ], + "recurrent otitis media": [ + "HP:0000403" + ], + "frequent otitis medium": [ + "HP:0000403" + ], + "frequent otitis media": [ + "HP:0000403" + ], + "multiple episode of otitis medium": [ + "HP:0000403" + ], + "multiple episodes of otitis media": [ + "HP:0000403" + ], + "otitis medium , recurrent": [ + "HP:0000403" + ], + "otitis media , recurrent": [ + "HP:0000403" + ], + "recurrent episode of otitis medium": [ + "HP:0000403" + ], + "recurrent episodes of otitis media": [ + "HP:0000403" + ], + "recurrent middle ear infection": [ + "HP:0000403" + ], + "susceptibility to otitis medium": [ + "HP:0000403" + ], + "susceptibility to otitis media": [ + "HP:0000403" + ], + "conductive hearing impairment": [ + "HP:0000405" + ], + "conduction deafness": [ + "HP:0000405" + ], + "conductive deafness": [ + "HP:0000405" + ], + "conductive hearing loss": [ + "HP:0000405" + ], + "hearing loss , conductive": [ + "HP:0000405" + ], + "sensorineural hearing impairment": [ + "HP:0000407" + ], + "hearing loss , sensorineural": [ + "HP:0000407" + ], + "sensorineural deafness": [ + "HP:0000407" + ], + "sensorineural hearing loss": [ + "HP:0000407" + ], + "progressive sensorineural hearing impairment": [ + "HP:0000408" + ], + "bilateral progressive sensorineural hearing loss": [ + "HP:0000408" + ], + "hearing loss , progressive sensorineural": [ + "HP:0000408" + ], + "hearing loss , sensorineural , bilateral , progressive": [ + "HP:0000408" + ], + "hearing loss , sensorineural , progressive": [ + "HP:0000408" + ], + "progressive bilateral sensorineural hearing loss": [ + "HP:0000408" + ], + "sensorineural hearing loss , progressive": [ + "HP:0000408" + ], + "mixed hearing impairment": [ + "HP:0000410" + ], + "hearing loss , mixed": [ + "HP:0000410" + ], + "mixed hearing loss": [ + "HP:0000410" + ], + "protrude ear": [ + "HP:0000411" + ], + "protruding ear": [ + "HP:0000411" + ], + "prominent ear": [ + "HP:0000411" + ], + "prominent ears": [ + "HP:0000411" + ], + "protruding ears": [ + "HP:0000411" + ], + "atresia of the external auditory canal": [ + "HP:0000413" + ], + "absent auditory canal": [ + "HP:0000413" + ], + "absent auditory canals": [ + "HP:0000413" + ], + "absent ear canal": [ + "HP:0000413" + ], + "absent external auditory canal": [ + "HP:0000413" + ], + "absent external auditory canals": [ + "HP:0000413" + ], + "atresia of the external auditory canals": [ + "HP:0000413" + ], + "atretic auditory canal": [ + "HP:0000413" + ], + "atretic auditory canals": [ + "HP:0000413" + ], + "atretic external auditory canal": [ + "HP:0000413" + ], + "atretic external auditory canals": [ + "HP:0000413" + ], + "auditory canal atresia": [ + "HP:0000413" + ], + "external acoustic meatus atresia": [ + "HP:0000413" + ], + "external auditory canal atresia": [ + "HP:0000413" + ], + "external auditory meatal atresia": [ + "HP:0000413" + ], + "external auditory meatus atresia": [ + "HP:0000413" + ], + "bulbous nose": [ + "HP:0000414" + ], + "bulbous nasal tip": [ + "HP:0000414" + ], + "potato nose": [ + "HP:0000414" + ], + "abnormality of the choanae": [ + "HP:0000415" + ], + "slender nose": [ + "HP:0000417" + ], + "narrow nasal ridge": [ + "HP:0000418" + ], + "decrease width of dorsum of nose": [ + "HP:0000418" + ], + "decreased width of dorsum of nose": [ + "HP:0000418" + ], + "decrease width of nasal dorsum": [ + "HP:0000418" + ], + "decreased width of nasal dorsum": [ + "HP:0000418" + ], + "decrease width of nasal ridge": [ + "HP:0000418" + ], + "decreased width of nasal ridge": [ + "HP:0000418" + ], + "narrow dorsum of nose": [ + "HP:0000418" + ], + "narrow nasal dorsum": [ + "HP:0000418" + ], + "pinch nose": [ + "HP:0000418" + ], + "pinched nose": [ + "HP:0000418" + ], + "thin dorsum of nose": [ + "HP:0000418" + ], + "thin nasal dorsum": [ + "HP:0000418" + ], + "thin nasal ridge": [ + "HP:0000418" + ], + "abnormality of the nasal septum": [ + "HP:0000419" + ], + "abnormality of septum of nose": [ + "HP:0000419" + ], + "anomaly of nasal septum": [ + "HP:0000419" + ], + "anomaly of septum of nose": [ + "HP:0000419" + ], + "short nasal septum": [ + "HP:0000420" + ], + "decreased length of nasal septum": [ + "HP:0000420" + ], + "decreased length of septum of nose": [ + "HP:0000420" + ], + "short septum of nose": [ + "HP:0000420" + ], + "epistaxis": [ + "HP:0000421" + ], + "bloody nose": [ + "HP:0000421" + ], + "frequent nosebleed": [ + "HP:0000421" + ], + "frequent nosebleeds": [ + "HP:0000421" + ], + "nasal haemorrhage": [ + "HP:0000421" + ], + "nasal hemorrhage": [ + "HP:0000421" + ], + "nose bleed": [ + "HP:0000421" + ], + "nose bleeding": [ + "HP:0000421" + ], + "nosebleed": [ + "HP:0000421" + ], + "abnormal nasal bridge morphology": [ + "HP:0000422" + ], + "abnormality of the bridge of the nose": [ + "HP:0000422" + ], + "abnormality of the nasal bridge": [ + "HP:0000422" + ], + "abnormality of the nasal root": [ + "HP:0000422" + ], + "deformity of the bridge of the nose": [ + "HP:0000422" + ], + "deformity of the nasal bridge": [ + "HP:0000422" + ], + "malformation of the bridge of the nose": [ + "HP:0000422" + ], + "malformation of the nasal bridge": [ + "HP:0000422" + ], + "prominent nasal bridge": [ + "HP:0000426" + ], + "convex bridge of nose": [ + "HP:0000426" + ], + "convex nasal bridge": [ + "HP:0000426" + ], + "elevate nasal bridge": [ + "HP:0000426" + ], + "elevated nasal bridge": [ + "HP:0000426" + ], + "high nasal bridge": [ + "HP:0000426" + ], + "prominent bridge of nose": [ + "HP:0000426" + ], + "prominent nasal root": [ + "HP:0000426" + ], + "protrude bridge of nose": [ + "HP:0000426" + ], + "protruding bridge of nose": [ + "HP:0000426" + ], + "protrude nasal bridge": [ + "HP:0000426" + ], + "protruding nasal bridge": [ + "HP:0000426" + ], + "abnormality of the nasal ala": [ + "HP:0000429" + ], + "abnormality of the nasal alae": [ + "HP:0000429" + ], + "abnormality of the nasal alar cartilage": [ + "HP:0000429" + ], + "deformity of the nasal ala": [ + "HP:0000429" + ], + "deformity of the nasal alar cartilage": [ + "HP:0000429" + ], + "malformation of the nasal ala": [ + "HP:0000429" + ], + "malformation of the nasal alar cartilage": [ + "HP:0000429" + ], + "underdeveloped nasal ala": [ + "HP:0000430" + ], + "underdeveloped nasal alae": [ + "HP:0000430" + ], + "ala nasi , underdevelop": [ + "HP:0000430" + ], + "ala nasi , underdeveloped": [ + "HP:0000430" + ], + "alar cartilage hypoplasia": [ + "HP:0000430" + ], + "decreased size of nasal ala": [ + "HP:0000430" + ], + "decreased size of nasal alae": [ + "HP:0000430" + ], + "hypoplastic ala nasae": [ + "HP:0000430" + ], + "hypoplastic alae nasae": [ + "HP:0000430" + ], + "hypoplastic ala nasi": [ + "HP:0000430" + ], + "hypoplastic alae nasi": [ + "HP:0000430" + ], + "hypoplastic alar cartilage": [ + "HP:0000430" + ], + "hypoplastic alar nasae": [ + "HP:0000430" + ], + "hypoplastic naris": [ + "HP:0000430" + ], + "hypoplastic nares": [ + "HP:0000430" + ], + "hypoplastic nasal ala": [ + "HP:0000430" + ], + "hypoplastic nasal alae": [ + "HP:0000430" + ], + "hypoplastic nasal wing": [ + "HP:0000430" + ], + "hypoplastic nasal wings": [ + "HP:0000430" + ], + "hypoplastic nostril": [ + "HP:0000430" + ], + "hypoplastic nostrils": [ + "HP:0000430" + ], + "nasal cartilage hypoplasia": [ + "HP:0000430" + ], + "small nasal ala": [ + "HP:0000430" + ], + "small nasal alae": [ + "HP:0000430" + ], + "thin hypoplastic ala nasi": [ + "HP:0000430" + ], + "thin hypoplastic alae nasi": [ + "HP:0000430" + ], + "underdeveloped tissue around nostril": [ + "HP:0000430" + ], + "wide nasal bridge": [ + "HP:0000431" + ], + "broad flat nasal bridge": [ + "HP:0000431" + ], + "broad nasal bridge": [ + "HP:0000431" + ], + "broad nasal root": [ + "HP:0000431" + ], + "broaden nasal bridge": [ + "HP:0000431" + ], + "broadened nasal bridge": [ + "HP:0000431" + ], + "increase breadth of bridge of nose": [ + "HP:0000431" + ], + "increased breadth of bridge of nose": [ + "HP:0000431" + ], + "increase breadth of nasal bridge": [ + "HP:0000431" + ], + "increased breadth of nasal bridge": [ + "HP:0000431" + ], + "increase width of bridge of nose": [ + "HP:0000431" + ], + "increased width of bridge of nose": [ + "HP:0000431" + ], + "increase width of nasal bridge": [ + "HP:0000431" + ], + "increased width of nasal bridge": [ + "HP:0000431" + ], + "nasal bridge broad": [ + "HP:0000431" + ], + "nasal bridge , wide": [ + "HP:0000431" + ], + "wide bridge of nose": [ + "HP:0000431" + ], + "widen nasal bridge": [ + "HP:0000431" + ], + "widened nasal bridge": [ + "HP:0000431" + ], + "abnormal nasal mucosa morphology": [ + "HP:0000433" + ], + "abnormality of mucosa of nose": [ + "HP:0000433" + ], + "abnormality of mucous membrane of nose": [ + "HP:0000433" + ], + "abnormality of nasal mucous membrane": [ + "HP:0000433" + ], + "abnormality of the nasal mucosa": [ + "HP:0000433" + ], + "nasal mucosa telangiectasia": [ + "HP:0000434" + ], + "angioectasia of mucosa of nose": [ + "HP:0000434" + ], + "angioectasia of mucous membrane of nose": [ + "HP:0000434" + ], + "angioectasia of nasal mucous membrane": [ + "HP:0000434" + ], + "nasal mucous membrane telangiectasia": [ + "HP:0000434" + ], + "spider vein of mucosa of nose": [ + "HP:0000434" + ], + "spider veins of mucosa of nose": [ + "HP:0000434" + ], + "spider vein of mucous membrane of nose": [ + "HP:0000434" + ], + "spider veins of mucous membrane of nose": [ + "HP:0000434" + ], + "spider vein of nasal mucous membrane": [ + "HP:0000434" + ], + "spider veins of nasal mucous membrane": [ + "HP:0000434" + ], + "telangiectasia of mucosa of nose": [ + "HP:0000434" + ], + "telangiectasia of mucous membrane of nose": [ + "HP:0000434" + ], + "telangiectasia of nasal mucous membrane": [ + "HP:0000434" + ], + "abnormality of the nasal tip": [ + "HP:0000436" + ], + "abnormality of tip of nose": [ + "HP:0000436" + ], + "deformity of the nasal tip": [ + "HP:0000436" + ], + "deformity of tip of nose": [ + "HP:0000436" + ], + "malformation of the nasal tip": [ + "HP:0000436" + ], + "malformation of tip of nose": [ + "HP:0000436" + ], + "depress nasal tip": [ + "HP:0000437" + ], + "depressed nasal tip": [ + "HP:0000437" + ], + "cave in nasal tip": [ + "HP:0000437" + ], + "caved in nasal tip": [ + "HP:0000437" + ], + "depressed tip of nose": [ + "HP:0000437" + ], + "flat nasal tip": [ + "HP:0000437" + ], + "flat tip of nose": [ + "HP:0000437" + ], + "flatten nasal tip": [ + "HP:0000437" + ], + "flattened nasal tip": [ + "HP:0000437" + ], + "nasal tip , depress": [ + "HP:0000437" + ], + "nasal tip , depressed": [ + "HP:0000437" + ], + "nasal tip , recess": [ + "HP:0000437" + ], + "nasal tip , recessed": [ + "HP:0000437" + ], + "nasal tip , retruded": [ + "HP:0000437" + ], + "retruded tip of nose": [ + "HP:0000437" + ], + "convex nasal ridge": [ + "HP:0000444" + ], + "beak nose": [ + "HP:0000444" + ], + "beaked nose": [ + "HP:0000444" + ], + "beaklike protrusion": [ + "HP:0000444" + ], + "convex dorsum of nose": [ + "HP:0000444" + ], + "convex nasal dorsum": [ + "HP:0000444" + ], + "hook nose": [ + "HP:0000444" + ], + "hooked nose": [ + "HP:0000444" + ], + "polly beak nasal deformity": [ + "HP:0000444" + ], + "wide nose": [ + "HP:0000445" + ], + "broad nose": [ + "HP:0000445" + ], + "increase breadth of nose": [ + "HP:0000445" + ], + "increased breadth of nose": [ + "HP:0000445" + ], + "increase nasal breadth": [ + "HP:0000445" + ], + "increased nasal breadth": [ + "HP:0000445" + ], + "increase nasal width": [ + "HP:0000445" + ], + "increased nasal width": [ + "HP:0000445" + ], + "increase width of nose": [ + "HP:0000445" + ], + "increased width of nose": [ + "HP:0000445" + ], + "narrow nasal bridge": [ + "HP:0000446" + ], + "narrow bridge of nose": [ + "HP:0000446" + ], + "narrow nasal root": [ + "HP:0000446" + ], + "nasal bridge , narrow": [ + "HP:0000446" + ], + "nasal bridge , thin": [ + "HP:0000446" + ], + "pinch bridge of nose": [ + "HP:0000446" + ], + "pinched bridge of nose": [ + "HP:0000446" + ], + "pinch nasal bridge": [ + "HP:0000446" + ], + "pinched nasal bridge": [ + "HP:0000446" + ], + "pear - shape nose": [ + "HP:0000447" + ], + "pear - shaped nose": [ + "HP:0000447" + ], + "prominent nose": [ + "HP:0000448" + ], + "big nose": [ + "HP:0000448" + ], + "disproportionately large nose": [ + "HP:0000448" + ], + "hyperplasia of nose": [ + "HP:0000448" + ], + "hypertrophy of nose": [ + "HP:0000448" + ], + "increase nasal size": [ + "HP:0000448" + ], + "increased nasal size": [ + "HP:0000448" + ], + "increase size of nose": [ + "HP:0000448" + ], + "increased size of nose": [ + "HP:0000448" + ], + "large nose": [ + "HP:0000448" + ], + "nasal hyperplasia": [ + "HP:0000448" + ], + "nasal hypertrophy": [ + "HP:0000448" + ], + "pronounce nose": [ + "HP:0000448" + ], + "pronounced nose": [ + "HP:0000448" + ], + "triangular nasal tip": [ + "HP:0000451" + ], + "triangular shape tip of nose": [ + "HP:0000451" + ], + "triangular shaped tip of nose": [ + "HP:0000451" + ], + "choanal stenosis": [ + "HP:0000452" + ], + "coanal stenosis": [ + "HP:0000452" + ], + "narrowing of the rear opening of the nasal cavity": [ + "HP:0000452" + ], + "choanal atresia": [ + "HP:0000453" + ], + "blockage of the rear opening of the nasal cavity": [ + "HP:0000453" + ], + "obstruction of the rear opening of the nasal cavity": [ + "HP:0000453" + ], + "flare nostril": [ + "HP:0000454" + ], + "flared nostrils": [ + "HP:0000454" + ], + "flare nasal ala": [ + "HP:0000454" + ], + "flared nasal alae": [ + "HP:0000454" + ], + "broad nasal tip": [ + "HP:0000455" + ], + "broad tip of nose": [ + "HP:0000455" + ], + "broad upturned nose": [ + "HP:0000455" + ], + "broad , upturned nose": [ + "HP:0000455" + ], + "increase breadth of nasal tip": [ + "HP:0000455" + ], + "increased breadth of nasal tip": [ + "HP:0000455" + ], + "increase breadth of tip of nose": [ + "HP:0000455" + ], + "increased breadth of tip of nose": [ + "HP:0000455" + ], + "increase width of nasal tip": [ + "HP:0000455" + ], + "increased width of nasal tip": [ + "HP:0000455" + ], + "increase width of tip of nose": [ + "HP:0000455" + ], + "increased width of tip of nose": [ + "HP:0000455" + ], + "nasal tip , broad": [ + "HP:0000455" + ], + "nasal tip , wide": [ + "HP:0000455" + ], + "wide tip of nose": [ + "HP:0000455" + ], + "bifid nasal tip": [ + "HP:0000456" + ], + "bifid tip of nose": [ + "HP:0000456" + ], + "cleft nasal tip": [ + "HP:0000456" + ], + "cleft tip of nose": [ + "HP:0000456" + ], + "notch nasal tip": [ + "HP:0000456" + ], + "notched nasal tip": [ + "HP:0000456" + ], + "notched tip of nose": [ + "HP:0000456" + ], + "depress nasal ridge": [ + "HP:0000457" + ], + "depressed nasal ridge": [ + "HP:0000457" + ], + "depressed dorsum of nose": [ + "HP:0000457" + ], + "depress nasal dorsum": [ + "HP:0000457" + ], + "depressed nasal dorsum": [ + "HP:0000457" + ], + "flat dorsum of nose": [ + "HP:0000457" + ], + "flat nasal dorsum": [ + "HP:0000457" + ], + "flat nose": [ + "HP:0000457" + ], + "recess dorsum of nose": [ + "HP:0000457" + ], + "recessed dorsum of nose": [ + "HP:0000457" + ], + "recess nasal dorsum": [ + "HP:0000457" + ], + "recessed nasal dorsum": [ + "HP:0000457" + ], + "recess nasal ridge": [ + "HP:0000457" + ], + "recessed nasal ridge": [ + "HP:0000457" + ], + "retruded dorsum of nose": [ + "HP:0000457" + ], + "retruded nasal dorsum": [ + "HP:0000457" + ], + "retruded nasal ridge": [ + "HP:0000457" + ], + "anosmia": [ + "HP:0000458" + ], + "loss of smell": [ + "HP:0000458" + ], + "lose smell": [ + "HP:0000458" + ], + "lost smell": [ + "HP:0000458" + ], + "narrow nose": [ + "HP:0000460" + ], + "decrease nasal breadth": [ + "HP:0000460" + ], + "decreased nasal breadth": [ + "HP:0000460" + ], + "decrease nasal width": [ + "HP:0000460" + ], + "decreased nasal width": [ + "HP:0000460" + ], + "thin nose": [ + "HP:0000460" + ], + "anteverted naris": [ + "HP:0000463" + ], + "anteverted nares": [ + "HP:0000463" + ], + "anteverted nose": [ + "HP:0000463" + ], + "anteverted nostril": [ + "HP:0000463" + ], + "anteverted nostrils": [ + "HP:0000463" + ], + "nasal tip , upturned": [ + "HP:0000463" + ], + "nostril anteverted": [ + "HP:0000463" + ], + "nostrils anteverted": [ + "HP:0000463" + ], + "upturned naris": [ + "HP:0000463" + ], + "upturned nares": [ + "HP:0000463" + ], + "upturned nasal tip": [ + "HP:0000463" + ], + "upturned nasal tips": [ + "HP:0000463" + ], + "upturned nose": [ + "HP:0000463" + ], + "upturned nostril": [ + "HP:0000463" + ], + "upturned nostrils": [ + "HP:0000463" + ], + "abnormality of the neck": [ + "HP:0000464" + ], + "anomaly of the neck": [ + "HP:0000464" + ], + "deformity of the neck": [ + "HP:0000464" + ], + "malformation of the neck": [ + "HP:0000464" + ], + "web neck": [ + "HP:0000465" + ], + "webbed neck": [ + "HP:0000465" + ], + "neck web": [ + "HP:0000465" + ], + "neck webbing": [ + "HP:0000465" + ], + "pterygium colli": [ + "HP:0000465" + ], + "limited neck range of motion": [ + "HP:0000466" + ], + "limited cervical range of motion": [ + "HP:0000466" + ], + "neck muscle weakness": [ + "HP:0000467" + ], + "flaccid neck": [ + "HP:0000467" + ], + "floppy neck": [ + "HP:0000467" + ], + "increase adipose tissue around the neck": [ + "HP:0000468" + ], + "increased adipose tissue around the neck": [ + "HP:0000468" + ], + "increase fat around the neck": [ + "HP:0000468" + ], + "increased fat around the neck": [ + "HP:0000468" + ], + "short neck": [ + "HP:0000470" + ], + "cervical shortening": [ + "HP:0000470" + ], + "decreased cervical height": [ + "HP:0000470" + ], + "decreased cervical length": [ + "HP:0000470" + ], + "decreased length of neck": [ + "HP:0000470" + ], + "gastrointestinal angiodysplasia": [ + "HP:0000471" + ], + "gi angiodysplasia": [ + "HP:0000471" + ], + "long neck": [ + "HP:0000472" + ], + "cervical elongation": [ + "HP:0000472" + ], + "elongate neck": [ + "HP:0000472" + ], + "elongated neck": [ + "HP:0000472" + ], + "increased cervical length": [ + "HP:0000472" + ], + "increased length of neck": [ + "HP:0000472" + ], + "torticollis": [ + "HP:0000473" + ], + "cervical dystonia": [ + "HP:0000473" + ], + "loxia": [ + "HP:0000473" + ], + "spasmodic torticollis": [ + "HP:0000473" + ], + "wry neck": [ + "HP:0000473" + ], + "thicken nuchal skin fold": [ + "HP:0000474" + ], + "thickened nuchal skin fold": [ + "HP:0000474" + ], + "excess nuchal skin": [ + "HP:0000474" + ], + "increase nuchal fold thickness": [ + "HP:0000474" + ], + "increased nuchal fold thickness": [ + "HP:0000474" + ], + "thicken nuchal skin": [ + "HP:0000474" + ], + "thickened nuchal skin": [ + "HP:0000474" + ], + "thicken skin fold of neck": [ + "HP:0000474" + ], + "thickened skin folds of neck": [ + "HP:0000474" + ], + "thicken skin over the neck": [ + "HP:0000474" + ], + "thickened skin over the neck": [ + "HP:0000474" + ], + "broad neck": [ + "HP:0000475" + ], + "increase width of neck": [ + "HP:0000475" + ], + "increased width of neck": [ + "HP:0000475" + ], + "thick neck": [ + "HP:0000475" + ], + "wide neck": [ + "HP:0000475" + ], + "cystic hygroma": [ + "HP:0000476" + ], + "cystic hygroma of the neck": [ + "HP:0000476" + ], + "abnormality of the eye": [ + "HP:0000478" + ], + "abnormal eye": [ + "HP:0000478" + ], + "eye disease": [ + "HP:0000478" + ], + "abnormal retinal morphology": [ + "HP:0000479" + ], + "abnormal retina": [ + "HP:0000479" + ], + "abnormality of the retina": [ + "HP:0000479" + ], + "anomaly of the retina": [ + "HP:0000479" + ], + "retina issue": [ + "HP:0000479" + ], + "retinal disease": [ + "HP:0000479" + ], + "retinal coloboma": [ + "HP:0000480" + ], + "hole in the back of the eye": [ + "HP:0000480" + ], + "abnormal cornea morphology": [ + "HP:0000481" + ], + "abnormality of the cornea": [ + "HP:0000481" + ], + "corneal abnormality": [ + "HP:0000481" + ], + "corneal abnormalities": [ + "HP:0000481" + ], + "cornela disease": [ + "HP:0000481" + ], + "microcornea": [ + "HP:0000482" + ], + "cornea of eye less than 10mm in diameter": [ + "HP:0000482" + ], + "decrease corneal diameter": [ + "HP:0000482" + ], + "decreased corneal diameter": [ + "HP:0000482" + ], + "astigmatism": [ + "HP:0000483" + ], + "abnormal curving of the cornea or lens of the eye": [ + "HP:0000483" + ], + "hyperopic astigmatism": [ + "HP:0000484" + ], + "megalocornea": [ + "HP:0000485" + ], + "anterior megalophthalmos": [ + "HP:0000485" + ], + "enlarge cornea": [ + "HP:0000485" + ], + "enlarged cornea": [ + "HP:0000485" + ], + "increase corneal diameter": [ + "HP:0000485" + ], + "increased corneal diameter": [ + "HP:0000485" + ], + "macrocornea": [ + "HP:0000485" + ], + "strabismus": [ + "HP:0000486" + ], + "cross - eyed": [ + "HP:0000486" + ], + "squint": [ + "HP:0000486" + ], + "squint eye": [ + "HP:0000486" + ], + "squint eyes": [ + "HP:0000486" + ], + "obsolete congenital strabismus": [ + "HP:0000487" + ], + "retinopathy": [ + "HP:0000488" + ], + "noninflammatory retina disease": [ + "HP:0000488" + ], + "obsolete abnormality of globe location or size": [ + "HP:0000489" + ], + "deeply set eye": [ + "HP:0000490" + ], + "deep set eye": [ + "HP:0000490" + ], + "deep - set eye": [ + "HP:0000490" + ], + "deep - set eyes": [ + "HP:0000490" + ], + "enophthalmos": [ + "HP:0000490" + ], + "ocular depression": [ + "HP:0000490" + ], + "sink eye": [ + "HP:0000490" + ], + "sunken eye": [ + "HP:0000490" + ], + "sunken eyes": [ + "HP:0000490" + ], + "keratitis": [ + "HP:0000491" + ], + "corneal inflammation": [ + "HP:0000491" + ], + "abnormal eyelid morphology": [ + "HP:0000492" + ], + "abnormality of the eyelid": [ + "HP:0000492" + ], + "abnormality of the eyelids": [ + "HP:0000492" + ], + "abnormal foveal morphology": [ + "HP:0000493" + ], + "abnormality of the fovea": [ + "HP:0000493" + ], + "downslanted palpebral fissure": [ + "HP:0000494" + ], + "downslanted palpebral fissures": [ + "HP:0000494" + ], + "antimongoloid eye slant": [ + "HP:0000494" + ], + "antimongoloid slant of palpebral fissure": [ + "HP:0000494" + ], + "antimongoloid slant of palpebral fissures": [ + "HP:0000494" + ], + "antimongoloid slant palpebral fissure": [ + "HP:0000494" + ], + "antimongoloid slanted palpebral fissures": [ + "HP:0000494" + ], + "down slant palpebral fissure": [ + "HP:0000494" + ], + "down slanting palpebral fissures": [ + "HP:0000494" + ], + "down - slanted palpebral fissure": [ + "HP:0000494" + ], + "down - slanted palpebral fissures": [ + "HP:0000494" + ], + "down - slant palpebral fissure": [ + "HP:0000494" + ], + "down - slanting palpebral fissure": [ + "HP:0000494" + ], + "down - slanting palpebral fissures": [ + "HP:0000494" + ], + "downslanting palpebral fissure": [ + "HP:0000494" + ], + "downslanting palpebral fissures": [ + "HP:0000494" + ], + "downward slant palpebral fissure": [ + "HP:0000494" + ], + "downward slanted palpebral fissures": [ + "HP:0000494" + ], + "downward slanting of the opening between the eyelid": [ + "HP:0000494" + ], + "downward slanting of the opening between the eyelids": [ + "HP:0000494" + ], + "downward slanting palpebral fissures": [ + "HP:0000494" + ], + "downward - slant palpebral fissure": [ + "HP:0000494" + ], + "downward - slanting palpebral fissures": [ + "HP:0000494" + ], + "palpebral fissure down - slanted": [ + "HP:0000494" + ], + "palpebral fissures down - slanted": [ + "HP:0000494" + ], + "recurrent corneal erosion": [ + "HP:0000495" + ], + "recurrent corneal erosions": [ + "HP:0000495" + ], + "corneal erosion , recurrent": [ + "HP:0000495" + ], + "corneal erosions , recurrent": [ + "HP:0000495" + ], + "epithelial corneal erosion": [ + "HP:0000495" + ], + "epithelial corneal erosions": [ + "HP:0000495" + ], + "recurrent breakdown of clear protective layer of eye": [ + "HP:0000495" + ], + "recurrent corneal ulceration": [ + "HP:0000495" + ], + "recurrent corneal ulcerations": [ + "HP:0000495" + ], + "abnormality of eye movement": [ + "HP:0000496" + ], + "abnormal extraocular movement": [ + "HP:0000496" + ], + "abnormal extraocular movements": [ + "HP:0000496" + ], + "abnormal eye motility": [ + "HP:0000496" + ], + "abnormal eye movement": [ + "HP:0000496" + ], + "abnormal eye movements": [ + "HP:0000496" + ], + "abnormal motility of the globe of the eye": [ + "HP:0000496" + ], + "abnormal movement of the globe of the eye": [ + "HP:0000496" + ], + "abnormal ocular movement": [ + "HP:0000496" + ], + "abnormal ocular movements": [ + "HP:0000496" + ], + "eye movement abnormality": [ + "HP:0000496" + ], + "eye movement abnormalities": [ + "HP:0000496" + ], + "eye movement issue": [ + "HP:0000496" + ], + "ocular movement abnormality": [ + "HP:0000496" + ], + "ocular movement abnormalities": [ + "HP:0000496" + ], + "oculomotor abnormality": [ + "HP:0000496" + ], + "oculomotor abnormalities": [ + "HP:0000496" + ], + "globe retraction and deviation on abduction": [ + "HP:0000497" + ], + "blepharitis": [ + "HP:0000498" + ], + "cellulitis of eyelid": [ + "HP:0000498" + ], + "cellulitis of eyelids": [ + "HP:0000498" + ], + "inflammation of eyelid": [ + "HP:0000498" + ], + "inflammation of eyelids": [ + "HP:0000498" + ], + "abnormal eyelash morphology": [ + "HP:0000499" + ], + "abnormal eyelash": [ + "HP:0000499" + ], + "abnormal eyelashes": [ + "HP:0000499" + ], + "abnormality of the eyelash": [ + "HP:0000499" + ], + "abnormality of the eyelashes": [ + "HP:0000499" + ], + "eyelash abnormality": [ + "HP:0000499" + ], + "glaucoma": [ + "HP:0000501" + ], + "abnormal conjunctiva morphology": [ + "HP:0000502" + ], + "tortuosity of conjunctival vessel": [ + "HP:0000503" + ], + "tortuosity of conjunctival vessels": [ + "HP:0000503" + ], + "abnormality of vision": [ + "HP:0000504" + ], + "abnormality of sight": [ + "HP:0000504" + ], + "vision issue": [ + "HP:0000504" + ], + "visual impairment": [ + "HP:0000505" + ], + "impaired vision": [ + "HP:0000505" + ], + "loss of eyesight": [ + "HP:0000505" + ], + "poor vision": [ + "HP:0000505" + ], + "telecanthus": [ + "HP:0000506" + ], + "corner of eye widely separate": [ + "HP:0000506" + ], + "corners of eye widely separated": [ + "HP:0000506" + ], + "dystopia canthorum": [ + "HP:0000506" + ], + "increase distance between medial canthus": [ + "HP:0000506" + ], + "increased distance between medial canthi": [ + "HP:0000506" + ], + "increase intercanthal distance": [ + "HP:0000506" + ], + "increased intercanthal distance": [ + "HP:0000506" + ], + "ptosis": [ + "HP:0000508" + ], + "blepharoptosis": [ + "HP:0000508" + ], + "droop upper eyelid": [ + "HP:0000508" + ], + "drooping upper eyelid": [ + "HP:0000508" + ], + "eye drop": [ + "HP:0000508" + ], + "eyelid ptosis": [ + "HP:0000508" + ], + "conjunctivitis": [ + "HP:0000509" + ], + "conjunctivitis , recurrent": [ + "HP:0000509" + ], + "pink eye": [ + "HP:0000509" + ], + "rod - cone dystrophy": [ + "HP:0000510" + ], + "retinitis pigmentosa": [ + "HP:0000510" + ], + "rod cone dystrophy": [ + "HP:0000510" + ], + "vertical supranuclear gaze palsy": [ + "HP:0000511" + ], + "vertical gaze palsy": [ + "HP:0000511" + ], + "abnormal electroretinogram": [ + "HP:0000512" + ], + "abnormal electroretinography": [ + "HP:0000512" + ], + "abnormal erg": [ + "HP:0000512" + ], + "erg abnormal": [ + "HP:0000512" + ], + "slow saccadic eye movement": [ + "HP:0000514" + ], + "slow saccadic eye movements": [ + "HP:0000514" + ], + "slow eye movement": [ + "HP:0000514" + ], + "slow eye movements": [ + "HP:0000514" + ], + "slow saccade": [ + "HP:0000514" + ], + "slow saccades": [ + "HP:0000514" + ], + "slow visual tracking": [ + "HP:0000514" + ], + "abnormality of the lens": [ + "HP:0000517" + ], + "lens disease": [ + "HP:0000517" + ], + "lens issue": [ + "HP:0000517" + ], + "cataract": [ + "HP:0000518" + ], + "cataracts": [ + "HP:0000518" + ], + "clouding of the lens of the eye": [ + "HP:0000518" + ], + "cloudy lens": [ + "HP:0000518" + ], + "lens opacity": [ + "HP:0000518" + ], + "lens opacities": [ + "HP:0000518" + ], + "developmental cataract": [ + "HP:0000519" + ], + "bilateral congenital cataract": [ + "HP:0000519" + ], + "bilateral congenital cataracts": [ + "HP:0000519" + ], + "cataract , congenital": [ + "HP:0000519" + ], + "clouding of the lens of the eye at birth": [ + "HP:0000519" + ], + "congenital cataract": [ + "HP:0000519" + ], + "congenital cataracts": [ + "HP:0000519" + ], + "congenital cataract , bilateral": [ + "HP:0000519" + ], + "congenital cataracts , bilateral": [ + "HP:0000519" + ], + "proptosis": [ + "HP:0000520" + ], + "anterior bulging of the globe": [ + "HP:0000520" + ], + "anterior bulging of the globe of eye": [ + "HP:0000520" + ], + "bulge eye": [ + "HP:0000520" + ], + "bulging eye": [ + "HP:0000520" + ], + "exophthalmos": [ + "HP:0000520" + ], + "eyeball bulge out": [ + "HP:0000520" + ], + "eyeballs bulging out": [ + "HP:0000520" + ], + "ocular proptosis": [ + "HP:0000520" + ], + "prominent eye": [ + "HP:0000520" + ], + "prominent eyes": [ + "HP:0000520" + ], + "prominent globe": [ + "HP:0000520" + ], + "prominent globes": [ + "HP:0000520" + ], + "protrude eye": [ + "HP:0000520" + ], + "protruding eyes": [ + "HP:0000520" + ], + "protrusio bulbi": [ + "HP:0000520" + ], + "alacrima": [ + "HP:0000522" + ], + "absence of tear in the eye": [ + "HP:0000522" + ], + "absence of tears in the eyes": [ + "HP:0000522" + ], + "absent lacrimal fluid": [ + "HP:0000522" + ], + "absent lacrimal fluids": [ + "HP:0000522" + ], + "absent tear secretion": [ + "HP:0000522" + ], + "subcapsular cataract": [ + "HP:0000523" + ], + "subcapsular cataracts": [ + "HP:0000523" + ], + "subcapsular lenticular cataract": [ + "HP:0000523" + ], + "subcapsular lenticular cataracts": [ + "HP:0000523" + ], + "subcapsular opacity": [ + "HP:0000523" + ], + "subcapsular opacities": [ + "HP:0000523" + ], + "conjunctival telangiectasia": [ + "HP:0000524" + ], + "conjunctival telangiectases": [ + "HP:0000524" + ], + "small dilate blood vessel near membrane cover front of eye and eyelid": [ + "HP:0000524" + ], + "small dilated blood vessels near membrane covering front of eye and eyelids": [ + "HP:0000524" + ], + "telangiectasia , conjunctival": [ + "HP:0000524" + ], + "abnormality iris morphology": [ + "HP:0000525" + ], + "abnormality of the iris": [ + "HP:0000525" + ], + "aniridia": [ + "HP:0000526" + ], + "absent iris": [ + "HP:0000526" + ], + "long eyelash": [ + "HP:0000527" + ], + "long eyelashes": [ + "HP:0000527" + ], + "ciliary trichomegaly": [ + "HP:0000527" + ], + "eyelash trichomegaly": [ + "HP:0000527" + ], + "increased length of eyelash": [ + "HP:0000527" + ], + "increased length of eyelashes": [ + "HP:0000527" + ], + "unusually long eyelash": [ + "HP:0000527" + ], + "unusually long eyelashes": [ + "HP:0000527" + ], + "anophthalmia": [ + "HP:0000528" + ], + "absence of eyeball": [ + "HP:0000528" + ], + "absence of eyeballs": [ + "HP:0000528" + ], + "absence of globe of eye": [ + "HP:0000528" + ], + "absence of globes of eyes": [ + "HP:0000528" + ], + "anophthalmia , clinical": [ + "HP:0000528" + ], + "clinical anophthalmia , unilateral / bilateral": [ + "HP:0000528" + ], + "failure of development of eyeball": [ + "HP:0000528" + ], + "miss eyeball": [ + "HP:0000528" + ], + "missing eyeball": [ + "HP:0000528" + ], + "miss globe of eye": [ + "HP:0000528" + ], + "missing globe of eye": [ + "HP:0000528" + ], + "no eyeball": [ + "HP:0000528" + ], + "no globe of eye": [ + "HP:0000528" + ], + "ocular absence": [ + "HP:0000528" + ], + "progressive visual loss": [ + "HP:0000529" + ], + "decrease visual acuity , progressive": [ + "HP:0000529" + ], + "decreased visual acuity , progressive": [ + "HP:0000529" + ], + "loss of visual acuity": [ + "HP:0000529" + ], + "progressive loss of vision": [ + "HP:0000529" + ], + "progressive vision loss": [ + "HP:0000529" + ], + "progressive visual acuity loss": [ + "HP:0000529" + ], + "progressive visual impairment": [ + "HP:0000529" + ], + "slowly progressive visual loss": [ + "HP:0000529" + ], + "vision loss , progressive": [ + "HP:0000529" + ], + "visual loss , progressive": [ + "HP:0000529" + ], + "corneal crystal": [ + "HP:0000531" + ], + "corneal crystals": [ + "HP:0000531" + ], + "corneal deposit": [ + "HP:0000531" + ], + "corneal deposits": [ + "HP:0000531" + ], + "abnormal chorioretinal morphology": [ + "HP:0000532" + ], + "chorioretinal abnormality": [ + "HP:0000532" + ], + "chorioretinal atrophy": [ + "HP:0000533" + ], + "chorioretinal thinning": [ + "HP:0000533" + ], + "abnormal eyebrow morphology": [ + "HP:0000534" + ], + "abnormality of the eyebrow": [ + "HP:0000534" + ], + "sparse and thin eyebrow": [ + "HP:0000535" + ], + "thin , sparse eyebrow": [ + "HP:0000535" + ], + "thin , sparse eyebrows": [ + "HP:0000535" + ], + "epicanthus inversus": [ + "HP:0000537" + ], + "pseudopapilledema": [ + "HP:0000538" + ], + "abnormality of refraction": [ + "HP:0000539" + ], + "hypermetropia": [ + "HP:0000540" + ], + "farsightedness": [ + "HP:0000540" + ], + "hyperopia": [ + "HP:0000540" + ], + "long - sightedness": [ + "HP:0000540" + ], + "retinal detachment": [ + "HP:0000541" + ], + "detach retina": [ + "HP:0000541" + ], + "detached retina": [ + "HP:0000541" + ], + "impaired ocular adduction": [ + "HP:0000542" + ], + "optic disc pallor": [ + "HP:0000543" + ], + "disc pallor": [ + "HP:0000543" + ], + "optic disk pallor": [ + "HP:0000543" + ], + "pale optic disc": [ + "HP:0000543" + ], + "pale optic discs": [ + "HP:0000543" + ], + "pale optic disk": [ + "HP:0000543" + ], + "external ophthalmoplegia": [ + "HP:0000544" + ], + "chronic progressive external ophthalmoplegia": [ + "HP:0000544" + ], + "ophthalmoplegia externa": [ + "HP:0000544" + ], + "paralysis or weakness of muscle within or surround out part of eye": [ + "HP:0000544" + ], + "paralysis or weakness of muscles within or surrounding outer part of eye": [ + "HP:0000544" + ], + "progressive paralysis or weakness of muscle of eye motility": [ + "HP:0000544" + ], + "progressive paralysis or weakness of muscles of eye motility": [ + "HP:0000544" + ], + "progressive paralysis or weakness of muscle of eye movement": [ + "HP:0000544" + ], + "progressive paralysis or weakness of muscles of eye movement": [ + "HP:0000544" + ], + "myopia": [ + "HP:0000545" + ], + "close sight": [ + "HP:0000545" + ], + "close sighted": [ + "HP:0000545" + ], + "near sight": [ + "HP:0000545" + ], + "near sighted": [ + "HP:0000545" + ], + "near sightedness": [ + "HP:0000545" + ], + "nearsightedness": [ + "HP:0000545" + ], + "retinal degeneration": [ + "HP:0000546" + ], + "retina degeneration": [ + "HP:0000546" + ], + "obsolete tapetoretinal degeneration": [ + "HP:0000547" + ], + "retinotapetal degeneration": [ + "HP:0000547" + ], + "cone / cone - rod dystrophy": [ + "HP:0000548" + ], + "cone rod dystrophy": [ + "HP:0000548" + ], + "cone - rod retinal dystrophy": [ + "HP:0000548" + ], + "abnormal conjugate eye movement": [ + "HP:0000549" + ], + "disconjugate eye movement": [ + "HP:0000549" + ], + "disconjugate eye movements": [ + "HP:0000549" + ], + "undetectable electroretinogram": [ + "HP:0000550" + ], + "abolish electroretinogram": [ + "HP:0000550" + ], + "abolished electroretinogram": [ + "HP:0000550" + ], + "absent electroretinogram": [ + "HP:0000550" + ], + "extinction of electroretinogram": [ + "HP:0000550" + ], + "extinguish electroretinogram": [ + "HP:0000550" + ], + "extinguished electroretinogram": [ + "HP:0000550" + ], + "no light - evoked response on electroretinogram": [ + "HP:0000550" + ], + "undetectable erg": [ + "HP:0000550" + ], + "color vision defect": [ + "HP:0000551" + ], + "abnormal color vision": [ + "HP:0000551" + ], + "abnormal colour vision": [ + "HP:0000551" + ], + "abnormality of color vision": [ + "HP:0000551" + ], + "abnormality of 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"white pupillary reflex": [ + "HP:0000555" + ], + "retinal dystrophy": [ + "HP:0000556" + ], + "breakdown of light - sensitive cell in back of eye": [ + "HP:0000556" + ], + "breakdown of light - sensitive cells in back of eye": [ + "HP:0000556" + ], + "buphthalmos": [ + "HP:0000557" + ], + "enlarge eyeball": [ + "HP:0000557" + ], + "enlarged eyeball": [ + "HP:0000557" + ], + "rieger anomaly": [ + "HP:0000558" + ], + "corneal scar": [ + "HP:0000559" + ], + "corneal scarring": [ + "HP:0000559" + ], + "absent eyelash": [ + "HP:0000561" + ], + "absent eyelashes": [ + "HP:0000561" + ], + "agenesis of eyelash": [ + "HP:0000561" + ], + "agenesis of eyelashes": [ + "HP:0000561" + ], + "aplasia of eyelash": [ + "HP:0000561" + ], + "aplasia of eyelashes": [ + "HP:0000561" + ], + "atrichia of eyelash": [ + "HP:0000561" + ], + "atrichia of eyelashes": [ + "HP:0000561" + ], + "failure of development of eyelash": [ + "HP:0000561" + ], + "failure of development of eyelashes": [ + "HP:0000561" + ], + "keratoconus": [ + "HP:0000563" + ], + "bulge cornea": [ + "HP:0000563" + ], + "bulging cornea": [ + "HP:0000563" + ], + "conical cornea": [ + "HP:0000563" + ], + "lacrimal duct atresia": [ + "HP:0000564" + ], + "imperforate nasolacrimal duct": [ + "HP:0000564" + ], + "imperforate nasolacrimal ducts": [ + "HP:0000564" + ], + "nasolacrimal duct atresia": [ + "HP:0000564" + ], + "unopened tear duct": [ + "HP:0000564" + ], + "esotropia": [ + "HP:0000565" + ], + "inward turn cross eye": [ + "HP:0000565" + ], + "inward turning cross eyed": [ + "HP:0000565" + ], + "chorioretinal coloboma": [ + "HP:0000567" + ], + "birth defect that cause a hole in the innermost layer at the back of the eye": [ + "HP:0000567" + ], + "birth defect that causes a hole in the innermost layer at the back of the eye": [ + "HP:0000567" + ], + "choroid coloboma": [ + "HP:0000567" + ], + "choroidal coloboma": [ + "HP:0000567" + ], + "choroidoretinal coloboma": [ + "HP:0000567" + ], + "coloboma of choroid": [ + "HP:0000567" + ], + "microphthalmia": [ + "HP:0000568" + ], + "abnormally small eyeball": [ + "HP:0000568" + ], + "abnormally small globe of eye": [ + "HP:0000568" + ], + "decreased size of eyeball": [ + "HP:0000568", + "HP:0007633" + ], + "decreased size of globe of eye": [ + "HP:0000568", + "HP:0007633" + ], + "microphthalmos": [ + "HP:0000568" + ], + "nanophthalmos": [ + "HP:0000568" + ], + "abnormal saccadic eye movement": [ + "HP:0000570" + ], + "abnormal saccadic eye movements": [ + "HP:0000570" + ], + "abnormality of saccadic eye movement": [ + "HP:0000570" + ], + "abnormality of saccadic eye movements": [ + "HP:0000570" + ], + "impaired saccade": [ + "HP:0000570" + ], + "impaired saccades": [ + "HP:0000570" + ], + "hypometric saccade": [ + "HP:0000571" + ], + "hypometric saccades": [ + "HP:0000571" + ], + "visual loss": [ + "HP:0000572" + ], + "loss of vision": [ + "HP:0000572" + ], + "vision loss": [ + "HP:0000572" + ], + "retinal hemorrhage": [ + "HP:0000573" + ], + "retinal bleeding": [ + "HP:0000573" + ], + "retinal haemorrhage": [ + "HP:0000573" + ], + "retinal haemorrhages": [ + "HP:0000573" + ], + "retinal hemorrhages": [ + "HP:0000573" + ], + "thick eyebrow": [ + "HP:0000574" + ], + "bushy eyebrow": [ + "HP:0000574" + ], + "bushy eyebrows": [ + "HP:0000574" + ], + "dense eyebrow": [ + "HP:0000574" + ], + "heavy eyebrow": [ + "HP:0000574" + ], + "heavy eyebrows": [ + "HP:0000574" + ], + "hypertrichosis of the eyebrow": [ + "HP:0000574" + ], + "hypertrichosis of the eyebrows": [ + "HP:0000574" + ], + "prominent eyebrow": [ + "HP:0000574" + ], + "prominent eyebrows": [ + "HP:0000574" + ], + "thick eyebrows": [ + "HP:0000574" + ], + "scotoma": [ + "HP:0000575" + ], + "blind spot": [ + "HP:0000575" + ], + "centrocecal scotoma": [ + "HP:0000576" + ], + "exotropia": [ + "HP:0000577" + ], + "outward face eye ball": [ + "HP:0000577" + ], + "outward facing eye ball": [ + "HP:0000577" + ], + "nasolacrimal duct obstruction": [ + "HP:0000579" + ], + "block tear duct": [ + "HP:0000579" + ], + "blocked tear duct": [ + "HP:0000579" + ], + "lacrimal duct obstruction": [ + "HP:0000579" + ], + "pigmentary retinopathy": [ + "HP:0000580" + ], + "pigmentary retinal deposit": [ + "HP:0000580" + ], + "pigmentary retinal deposits": [ + "HP:0000580" + ], + "retinal pigment clump": [ + "HP:0000580" + ], + "retinal pigment clumping": [ + "HP:0000580" + ], + "retinal pigmentary clumping": [ + "HP:0000580" + ], + "retinal pigmentary degeneration": [ + "HP:0000580" + ], + "blepharophimosis": [ + "HP:0000581" + ], + "decrease width of palpebral fissure": [ + "HP:0000581" + ], + "decreased width of palpebral fissure": [ + "HP:0000581" + ], + "narrow opening between the eyelid": [ + "HP:0000581" + ], + "narrow opening between the eyelids": [ + "HP:0000581" + ], + "upslanted palpebral fissure": [ + "HP:0000582" + ], + "mongoloid slant": [ + "HP:0000582" + ], + "upslanted palpebral fissures": [ + "HP:0000582" + ], + "upslanting palpebral fissure": [ + "HP:0000582" + ], + "upslanting palpebral fissures": [ + "HP:0000582" + ], + "upward slant palpebral fissure": [ + "HP:0000582" + ], + "upward slanted palpebral fissures": [ + "HP:0000582" + ], + "upward slanting of palpebral fissure": [ + "HP:0000582" + ], + "upward slanting of palpebral fissures": [ + "HP:0000582" + ], + "upward slanting of the opening between the eyelid": [ + "HP:0000582" + ], + "upward slanting of the opening between the eyelids": [ + "HP:0000582" + ], + "upward slanting palpebral fissures": [ + "HP:0000582" + ], + "punctate corneal epithelial erosion": [ + "HP:0000584" + ], + "punctate corneal epithelial erosions": [ + "HP:0000584" + ], + "band keratopathy": [ + "HP:0000585" + ], + "calcific band keratopathy": [ + "HP:0000585" + ], + "shallow orbit": [ + "HP:0000586" + ], + "shallow orbits": [ + "HP:0000586" + ], + "decrease depth of eye socket": [ + "HP:0000586" + ], + "decreased depth of eye sockets": [ + "HP:0000586" + ], + "decrease depth of orbit": [ + "HP:0000586" + ], + "decreased depth of orbits": [ + "HP:0000586" + ], + "shallow eye socket": [ + "HP:0000586" + ], + "shallow eye sockets": [ + "HP:0000586" + ], + "small shallow orbit": [ + "HP:0000586" + ], + "small shallow orbits": [ + "HP:0000586" + ], + "abnormality of the optic nerve": [ + "HP:0000587" + ], + "optic nerve abnormality": [ + "HP:0000587" + ], + "optic nerve abnormalities": [ + "HP:0000587" + ], + "optic nerve issue": [ + "HP:0000587" + ], + "optic disc coloboma": [ + "HP:0000588" + ], + "coloboma of optic nerve": [ + "HP:0000588" + ], + "optic disk coloboma": [ + "HP:0000588" + ], + "optic nerve coloboma": [ + "HP:0000588" + ], + "coloboma": [ + "HP:0000589" + ], + "notch pupil": [ + "HP:0000589" + ], + "notched pupil": [ + "HP:0000589" + ], + "ocular coloboma": [ + "HP:0000589" + ], + "ocular colobomas": [ + "HP:0000589" + ], + "progressive external ophthalmoplegia": [ + "HP:0000590" + ], + "external ophthalmoplegia , progressive": [ + "HP:0000590" + ], + "abnormal sclera morphology": [ + "HP:0000591" + ], + "abnormality of the outer white part of eyeball": [ + "HP:0000591" + ], + "abnormality of the sclera": [ + "HP:0000591" + ], + "blue sclerae": [ + "HP:0000592" + ], + "blue out white part of eyeball": [ + "HP:0000592" + ], + "blue outer white part of eyeball": [ + "HP:0000592" + ], + "blue sclera": [ + "HP:0000592" + ], + "bluish sclerae": [ + "HP:0000592" + ], + "white of eye be a bluish - gray color": [ + "HP:0000592" + ], + "whites of eyes are a bluish - gray color": [ + "HP:0000592" + ], + "white of eye be a bluish - gray colour": [ + "HP:0000592" + ], + "whites of eyes are a bluish - gray colour": [ + "HP:0000592" + ], + "abnormal anterior chamber morphology": [ + "HP:0000593" + ], + "abnormality of the anterior chamber": [ + "HP:0000593" + ], + "anterior chamber anomaly": [ + "HP:0000593" + ], + "anterior chamber anomalies": [ + "HP:0000593" + ], + "ocular anterior chamber abnormality": [ + "HP:0000593" + ], + "shallow anterior chamber": [ + "HP:0000594" + ], + "ophthalmoparesis": [ + "HP:0000597" + ], + "extraocular muscle palsy": [ + "HP:0000597" + ], + "extraocular muscle paralysis": [ + "HP:0000597" + ], + "weakness of extraocular eye movement": [ + "HP:0000597" + ], + "weakness of muscle control eye movement": [ + "HP:0000597" + ], + "weakness of muscles controlling eye movement": [ + "HP:0000597" + ], + "abnormality of the ear": [ + "HP:0000598" + ], + "abnormality of the frontal hairline": [ + "HP:0000599" + ], + "abnormality of hairline at front of head": [ + "HP:0000599" + ], + "abnormality of the pharynx": [ + "HP:0000600" + ], + "hypotelorism": [ + "HP:0000601" + ], + "abnormally close eye": [ + "HP:0000601" + ], + "abnormally close eyes": [ + "HP:0000601" + ], + "closely spaced eye": [ + "HP:0000601" + ], + "closely spaced eyes": [ + "HP:0000601" + ], + "decrease distance between eye socket": [ + "HP:0000601" + ], + "decreased distance between eye sockets": [ + "HP:0000601" + ], + "decrease distance between eye": [ + "HP:0000601" + ], + "decreased distance between eyes": [ + "HP:0000601" + ], + "decrease interpupillary distance": [ + "HP:0000601" + ], + "decreased interpupillary distance": [ + "HP:0000601" + ], + "decrease orbital separation": [ + "HP:0000601" + ], + "decreased orbital separation": [ + "HP:0000601" + ], + "ocular hypotelorism": [ + "HP:0000601" + ], + "ophthalmoplegia": [ + "HP:0000602" + ], + "eye muscle paralysis": [ + "HP:0000602" + ], + "paralysis of extraocular eye movement": [ + "HP:0000602" + ], + "central scotoma": [ + "HP:0000603" + ], + "blind spot locate at fixation point": [ + "HP:0000603" + ], + "blind spot located at fixation point": [ + "HP:0000603" + ], + "central blind spot": [ + "HP:0000603" + ], + "central scotomata": [ + "HP:0000603" + ], + "supranuclear gaze palsy": [ + "HP:0000605" + ], + "supranuclear gaze paralysis": [ + "HP:0000605" + ], + "abnormality of the periorbital region": [ + "HP:0000606" + ], + "abnormality of the region around the eye socket": [ + "HP:0000606" + ], + "anomaly of the periorbital region": [ + "HP:0000606" + ], + "deformity of the periorbital region": [ + "HP:0000606" + ], + "malformation of the periorbital region": [ + "HP:0000606" + ], + "periorbital wrinkle": [ + "HP:0000607" + ], + "periorbital wrinkles": [ + "HP:0000607" + ], + "excess periorbital skin wrinkling": [ + "HP:0000607" + ], + "periorbital rhytids": [ + "HP:0000607" + ], + "periorbital wrinkling": [ + "HP:0000607" + ], + "wrinkle around the eye": [ + "HP:0000607" + ], + "wrinkles around the eyes": [ + "HP:0000607" + ], + "macular degeneration": [ + "HP:0000608" + ], + "pigment macular degeneration": [ + "HP:0000608" + ], + "pigmented macular degeneration": [ + "HP:0000608" + ], + "optic nerve hypoplasia": [ + "HP:0000609" + ], + "hypoplastic optic nerve": [ + "HP:0000609" + ], + "hypoplastic optic nerves": [ + "HP:0000609" + ], + "underdeveloped optic nerve": [ + "HP:0000609" + ], + "underdeveloped optic nerves": [ + "HP:0000609" + ], + "abnormal choroid morphology": [ + "HP:0000610" + ], + "abnormality of the choroid": [ + "HP:0000610" + ], + "choroid disease": [ + "HP:0000610" + ], + "obsolete choroid coloboma": [ + "HP:0000611" + ], + "iris coloboma": [ + "HP:0000612" + ], + "cat eye": [ + "HP:0000612" + ], + "coloboma of iris": [ + "HP:0000612" + ], + "coloboma of the iris": [ + "HP:0000612" + ], + "keyhole iris": [ + "HP:0000612" + ], + "photophobia": [ + "HP:0000613" + ], + "extreme sensitivity of the eye to light": [ + "HP:0000613" + ], + "extreme sensitivity of the eyes to light": [ + "HP:0000613" + ], + "light hypersensitivity": [ + "HP:0000613" + ], + "photodysphoria": [ + "HP:0000613" + ], + "abnormal nasolacrimal system morphology": [ + "HP:0000614" + ], + "abnormality of the nasolacrimal system": [ + "HP:0000614" + ], + "abnormal pupil morphology": [ + "HP:0000615" + ], + "abnormal pupillary morphology": [ + "HP:0000615" + ], + "abnormality of the pupil": [ + "HP:0000615" + ], + "pupillary abnormality": [ 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"HP:0000619" + ], + "dacryocystitis": [ + "HP:0000620" + ], + "dacrocystitis": [ + "HP:0000620" + ], + "infection of the lacrimal sac": [ + "HP:0000620" + ], + "entropion": [ + "HP:0000621" + ], + "eyelid fold in": [ + "HP:0000621" + ], + "eyelid folded in": [ + "HP:0000621" + ], + "eyelid turn in": [ + "HP:0000621" + ], + "eyelid turned in": [ + "HP:0000621" + ], + "invert eyelid": [ + "HP:0000621" + ], + "inverted eyelid": [ + "HP:0000621" + ], + "blur vision": [ + "HP:0000622" + ], + "blurred vision": [ + "HP:0000622" + ], + "supranuclear ophthalmoplegia": [ + "HP:0000623" + ], + "eyelid coloboma": [ + "HP:0000625" + ], + "cleft eyelid": [ + "HP:0000625" + ], + "full thickness defect of the eyelid": [ + "HP:0000625" + ], + "notch eyelid": [ + "HP:0000625" + ], + "notched eyelid": [ + "HP:0000625" + ], + "posterior embryotoxon": [ + "HP:0000627" + ], + "embryotoxon": [ + "HP:0000627" + ], + "periorbital fullness": [ + "HP:0000629" + ], + "fullness around the eye": [ + "HP:0000629" + ], + "fullness around the eyes": [ + "HP:0000629" + ], + "periorbital puffiness": [ + "HP:0000629" + ], + "periorbital swell": [ + "HP:0000629" + ], + "periorbital swelling": [ + "HP:0000629" + ], + "puffiness around eye": [ + "HP:0000629" + ], + "puffy eye": [ + "HP:0000629" + ], + "puffy eyes": [ + "HP:0000629" + ], + "swell around the eye": [ + "HP:0000629" + ], + "swelling around the eyes": [ + "HP:0000629" + ], + "abnormal retinal artery morphology": [ + "HP:0000630" + ], + "abnormality of retinal artery": [ + "HP:0000630" + ], + "abnormality of retinal arteries": [ + "HP:0000630" + ], + "retinal arterial abnormality": [ + "HP:0000630" + ], + "retinal arterial tortuosity": [ + "HP:0000631" + ], + "retinal artery tortuousity": [ + "HP:0000631" + ], + "lacrimation abnormality": [ + "HP:0000632" + ], + "abnormality of tear production": [ + "HP:0000632" + ], + "decrease lacrimation": [ + "HP:0000633" + ], + "decreased lacrimation": [ + "HP:0000633" + ], + "decrease tear secretion": [ 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fissures": [ + "HP:0000637" + ], + "wide opening between the eyelid": [ + "HP:0000637" + ], + "wide opening between the eyelids": [ + "HP:0000637" + ], + "wide palpebral fissure": [ + "HP:0000637" + ], + "wide palpebral fissures": [ + "HP:0000637" + ], + "nystagmus": [ + "HP:0000639" + ], + "involuntary , rapid , rhythmic eye movement": [ + "HP:0000639" + ], + "involuntary , rapid , rhythmic eye movements": [ + "HP:0000639" + ], + "gaze - evoke nystagmus": [ + "HP:0000640" + ], + "gaze - evoked nystagmus": [ + "HP:0000640" + ], + "dysmetric saccade": [ + "HP:0000641" + ], + "dysmetric saccades": [ + "HP:0000641" + ], + "dysmetric eye movement": [ + "HP:0000641" + ], + "dysmetric eye movements": [ + "HP:0000641" + ], + "dysmetric eye saccade": [ + "HP:0000641" + ], + "dysmetric eye saccades": [ + "HP:0000641" + ], + "uncoordinated eye movement": [ + "HP:0000641" + ], + "red - green dyschromatopsia": [ + "HP:0000642" + ], + "dyschromatopsia with red - green confusion": [ + "HP:0000642" + 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space": [ + "HP:0000692" + ], + "abnormal teeth spacing": [ + "HP:0000692" + ], + "abnormality of alignment of teeth": [ + "HP:0000692" + ], + "abnormality of position of teeth": [ + "HP:0000692" + ], + "abnormality of teeth space": [ + "HP:0000692" + ], + "abnormality of teeth spacing": [ + "HP:0000692" + ], + "crook teeth": [ + "HP:0000692" + ], + "crooked teeth": [ + "HP:0000692" + ], + "malaligned teeth": [ + "HP:0000692" + ], + "malposition of teeth": [ + "HP:0000692" + ], + "malpositioned teeth": [ + "HP:0000692" + ], + "misalignment of teeth": [ + "HP:0000692" + ], + "teeth , malposition": [ + "HP:0000692" + ], + "odontodysplasia": [ + "HP:0000694" + ], + "ghost teeth": [ + "HP:0000694" + ], + "shell teeth": [ + "HP:0000694" + ], + "teeth with dentinal dysplasia": [ + "HP:0000694" + ], + "teeth with thin dentin and large pulp chamber": [ + "HP:0000694" + ], + "teeth with thin dentin and large pulp chambers": [ + "HP:0000694" + ], + "teeth with type iii dentinogenesis 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lymphocytic thyroiditis": [ + "HP:0000872" + ], + "hashimoto 's thyroiditis": [ + "HP:0000872" + ], + "diabetes insipidus": [ + "HP:0000873" + ], + "episodic hypertension": [ + "HP:0000875" + ], + "intermittent high blood pressure": [ + "HP:0000875" + ], + "oligomenorrhea": [ + "HP:0000876" + ], + "light or infrequent menstrual period": [ + "HP:0000876" + ], + "light or infrequent menstrual periods": [ + "HP:0000876" + ], + "insulin - resistant diabetes mellitus at puberty": [ + "HP:0000877" + ], + "11 pair of rib": [ + "HP:0000878" + ], + "11 pairs of ribs": [ + "HP:0000878" + ], + "short sternum": [ + "HP:0000879" + ], + "hypoplastic sternum": [ + "HP:0000879" + ], + "hypoplastic scapula": [ + "HP:0000882" + ], + "hypoplastic scapulae": [ + "HP:0000882" + ], + "scapular hypoplasia": [ + "HP:0000882" + ], + "short scapula": [ + "HP:0000882" + ], + "short scapulae": [ + "HP:0000882" + ], + "small scapula": [ + "HP:0000882" + ], + "small scapulae": [ + "HP:0000882" + ], + "small shoulder blade": [ + "HP:0000882" + ], + "thin rib": [ + "HP:0000883" + ], + "thin ribs": [ + "HP:0000883" + ], + "slender rib": [ + "HP:0000883" + ], + "slender ribs": [ + "HP:0000883" + ], + "prominent sternum": [ + "HP:0000884" + ], + "sternal protrusion": [ + "HP:0000884" + ], + "broad rib": [ + "HP:0000885" + ], + "broad ribs": [ + "HP:0000885" + ], + "wide rib": [ + "HP:0000885" + ], + "wide ribs": [ + "HP:0000885" + ], + "deform rib cage": [ + "HP:0000886" + ], + "deformed rib cage": [ + "HP:0000886" + ], + "cup rib": [ + "HP:0000887" + ], + "cupped ribs": [ + "HP:0000887" + ], + "rib cup": [ + "HP:0000887" + ], + "rib cupping": [ + "HP:0000887" + ], + "rib flaring": [ + "HP:0000887" + ], + "horizontal rib": [ + "HP:0000888" + ], + "horizontal ribs": [ + "HP:0000888" + ], + "abnormal clavicle morphology": [ + "HP:0000889" + ], + "abnormal clavicle": [ + "HP:0000889" + ], + "abnormal clavicles": [ + "HP:0000889" + ], + "abnormal collarbone": [ + "HP:0000889" + ], + "abnormality 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"HP:0000894" + ], + "lateral clavicle hook": [ + "HP:0000895" + ], + "handlebar clavicle": [ + "HP:0000895" + ], + "hook - shaped clavicle": [ + "HP:0000895" + ], + "hook - shape collarbone": [ + "HP:0000895" + ], + "hook - shaped collarbone": [ + "HP:0000895" + ], + "hooked clavicle": [ + "HP:0000895" + ], + "rib exostosis": [ + "HP:0000896" + ], + "rib exostoses": [ + "HP:0000896" + ], + "rachitic rosary": [ + "HP:0000897" + ], + "thicken rib": [ + "HP:0000900" + ], + "thickened ribs": [ + "HP:0000900" + ], + "rib fusion": [ + "HP:0000902" + ], + "fuse rib": [ + "HP:0000902" + ], + "fused ribs": [ + "HP:0000902" + ], + "flaring of rib cage": [ + "HP:0000904" + ], + "anterior flaring of rib": [ + "HP:0000904" + ], + "anterior flaring of ribs": [ + "HP:0000904" + ], + "progressive clavicular acroosteolysis": [ + "HP:0000905" + ], + "progressive acroosteolysis of the clavicle": [ + "HP:0000905" + ], + "anterior rib cup": [ + "HP:0000907" + ], + "anterior rib cupping": [ + "HP:0000907" + ], + "anterior cupping of rib": [ + "HP:0000907" + ], + "anterior cupping of ribs": [ + "HP:0000907" + ], + "anteriorly splay rib": [ + "HP:0000907" + ], + "anteriorly splayed ribs": [ + "HP:0000907" + ], + "wide - cupped costochondral junction": [ + "HP:0000910" + ], + "wide - cupped costochondral junctions": [ + "HP:0000910" + ], + "flat glenoid fossa": [ + "HP:0000911" + ], + "sprengel anomaly": [ + "HP:0000912" + ], + "congenital , upward displacement of the scapula": [ + "HP:0000912" + ], + "high scapula": [ + "HP:0000912" + ], + "high shoulder blade": [ + "HP:0000912" + ], + "sprengel deformity": [ + "HP:0000912" + ], + "posterior rib fusion": [ + "HP:0000913" + ], + "shield chest": [ + "HP:0000914" + ], + "broad chest": [ + "HP:0000914" + ], + "pectus excavatum of inferior sternum": [ + "HP:0000915" + ], + "pectus excavatum inferiorly": [ + "HP:0000915" + ], + "broad clavicle": [ + "HP:0000916" + ], + "broad clavicles": [ + "HP:0000916" + ], + "broad collarbone": [ + "HP:0000916" + ], + "superior pectus carinatum": [ + "HP:0000917" + ], + "pectus carinatum superiorly": [ + "HP:0000917" + ], + "scapular exostosis": [ + "HP:0000918" + ], + "scapular exostoses": [ + "HP:0000918" + ], + "scapula exostosis": [ + "HP:0000918" + ], + "scapulae exostoses": [ + "HP:0000918" + ], + "shoulder bone exostoes": [ + "HP:0000918" + ], + "abnormality of the costochondral junction": [ + "HP:0000919" + ], + "costochondral juctions abnormal": [ + "HP:0000919" + ], + "enlargement of the costochondral junction": [ + "HP:0000920" + ], + "costochondral thickening": [ + "HP:0000920" + ], + "enlarged costochondral junction": [ + "HP:0000920" + ], + "enlarged costochondral junctions": [ + "HP:0000920" + ], + "prominent costochondral junction": [ + "HP:0000920" + ], + "wide costochondral junction": [ + "HP:0000920" + ], + "wide costochondral junctions": [ + "HP:0000920" + ], + "widen costochondral junction": [ + "HP:0000920" + ], + "widened costochondral junction": [ + "HP:0000920" + ], + "miss rib": [ + "HP:0000921" + ], + "missing ribs": [ + "HP:0000921" + ], + "absent rib": [ + "HP:0000921" + ], + "absent ribs": [ + "HP:0000921" + ], + "decrease rib number": [ + "HP:0000921" + ], + "decreased rib number": [ + "HP:0000921" + ], + "posterior rib cup": [ + "HP:0000922" + ], + "posterior rib cupping": [ + "HP:0000922" + ], + "anterior and posterior rib cup": [ + "HP:0000922" + ], + "anterior and posterior rib cupping": [ + "HP:0000922" + ], + "bead rib": [ + "HP:0000923" + ], + "beaded ribs": [ + "HP:0000923" + ], + "abnormality of the skeletal system": [ + "HP:0000924" + ], + "skeletal abnormality": [ + "HP:0000924" + ], + "skeletal abnormalities": [ + "HP:0000924" + ], + "skeletal anomaly": [ + "HP:0000924" + ], + "skeletal anomalies": [ + "HP:0000924" + ], + "abnormality of the vertebral column": [ + "HP:0000925" + ], + "abnormal spine": [ + "HP:0000925" + ], + "abnormal vertebral column": [ + "HP:0000925" + ], + "abnormality of the backbone": [ + 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long bones": [ + "HP:0000935" + ], + "osteopenia": [ + "HP:0000938" + ], + "generalise osteopenia": [ + "HP:0000938" + ], + "generalised osteopenia": [ + "HP:0000938" + ], + "generalize osteopenia": [ + "HP:0000938" + ], + "generalized osteopenia": [ + "HP:0000938" + ], + "osteopaenia": [ + "HP:0000938" + ], + "osteoporosis": [ + "HP:0000939" + ], + "abnormal diaphysis morphology": [ + "HP:0000940" + ], + "abnormal shape of shaft of long bone": [ + "HP:0000940" + ], + "abnormality involve the diaphysis of the limb": [ + "HP:0000940" + ], + "abnormality involving the diaphyses of the limbs": [ + "HP:0000940" + ], + "abnormality of shaft of long bone of the limb": [ + "HP:0000940", + "HP:0006504" + ], + "abnormality of shaft of long bone of the limbs": [ + "HP:0000940", + "HP:0006504" + ], + "abnormality of the diaphysis": [ + "HP:0000940" + ], + "abnormality of the diaphyses": [ + "HP:0000940" + ], + "anomaly of the limb diaphysis": [ + "HP:0000940" + ], + "anomaly of the limb diaphyses": [ + "HP:0000940" + ], + "anomaly of the limb diaphyses morphology": [ + "HP:0000940" + ], + "short diaphysis": [ + "HP:0000941" + ], + "short diaphyses": [ + "HP:0000941" + ], + "short shaft of long bone": [ + "HP:0000941" + ], + "dysostosis multiplex": [ + "HP:0000943" + ], + "abnormality of the metaphysis": [ + "HP:0000944" + ], + "abnormality of the wide portion of a long bone": [ + "HP:0000944" + ], + "hypoplastic ilium": [ + "HP:0000946" + ], + "hypoplastic ilia": [ + "HP:0000946" + ], + "short and small iliac bone": [ + "HP:0000946" + ], + "short and small iliac bones": [ + "HP:0000946" + ], + "small iliac bone": [ + "HP:0000946" + ], + "small iliac bones": [ + "HP:0000946" + ], + "small wing of the pelvic girdle": [ + "HP:0000946" + ], + "small wings of the pelvic girdle": [ + "HP:0000946" + ], + "dumbbell - shape long bone": [ + "HP:0000947" + ], + "dumbbell - shaped long bone": [ + "HP:0000947" + ], + "dumbbell widening of long bone metaphyses": [ + "HP:0000947" + 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[ + "HP:0000960" + ], + "spinal dimple": [ + "HP:0000960" + ], + "cyanosis": [ + "HP:0000961" + ], + "blue discoloration of the skin": [ + "HP:0000961" + ], + "hyperkeratosis": [ + "HP:0000962" + ], + "thin skin": [ + "HP:0000963" + ], + "eczema": [ + "HP:0000964" + ], + "cutis marmorata": [ + "HP:0000965" + ], + "hypohidrosis": [ + "HP:0000966" + ], + "decrease ability to sweat": [ + "HP:0000966" + ], + "decreased ability to sweat": [ + "HP:0000966" + ], + "decrease sweating": [ + "HP:0000966" + ], + "decreased sweating": [ + "HP:0000966" + ], + "inadequate sweating": [ + "HP:0000966" + ], + "oligohidrosis": [ + "HP:0000966" + ], + "sweating , decrease": [ + "HP:0000966" + ], + "sweating , decreased": [ + "HP:0000966" + ], + "petechia": [ + "HP:0000967" + ], + "petechiae": [ + "HP:0000967" + ], + "ectodermal dysplasia": [ + "HP:0000968" + ], + "edema": [ + "HP:0000969" + ], + "dropsy": [ + "HP:0000969" + ], + "fluid retention": [ + "HP:0000969" + ], + "hydrops": [ + "HP:0000969" + ], 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"palmoplantar keratosis": [ + "HP:0000972" + ], + "thick palm and sol": [ + "HP:0000972" + ], + "thick palms and soles": [ + "HP:0000972" + ], + "thicken palm and sol": [ + "HP:0000972" + ], + "thickened palms and soles": [ + "HP:0000972" + ], + "thickening of the outer layer of the skin of the palm and sol": [ + "HP:0000972" + ], + "thickening of the outer layer of the skin of the palms and soles": [ + "HP:0000972" + ], + "cutis laxa": [ + "HP:0000973" + ], + "chalazoderma": [ + "HP:0000973" + ], + "cutaneous laxity": [ + "HP:0000973" + ], + "dermatochalasia": [ + "HP:0000973" + ], + "dermatomegaly": [ + "HP:0000973" + ], + "elastolysis": [ + "HP:0000973" + ], + "generalise elastolysis": [ + "HP:0000973" + ], + "generalised elastolysis": [ + "HP:0000973" + ], + "generalize elastolysis": [ + "HP:0000973" + ], + "generalized elastolysis": [ + "HP:0000973" + ], + "hang skin": [ + "HP:0000973" + ], + "hanging skin": [ + "HP:0000973" + ], + "hypoelastic skin": [ + "HP:0000973" + ], + "inelastic skin": [ + "HP:0000973" + ], + "lax skin": [ + "HP:0000973" + ], + "loose and inelastic skin": [ + "HP:0000973" + ], + "loose skin": [ + "HP:0000973" + ], + "skin laxity": [ + "HP:0000973" + ], + "hyperextensible skin": [ + "HP:0000974" + ], + "hyperelastic skin": [ + "HP:0000974" + ], + "skin hyperelasticity": [ + "HP:0000974" + ], + "skin hyperextensibility": [ + "HP:0000974" + ], + "stretchable skin": [ + "HP:0000974" + ], + "hyperhidrosis": [ + "HP:0000975" + ], + "diaphoresis": [ + "HP:0000975" + ], + "excessive sweating": [ + "HP:0000975" + ], + "increase sweating": [ + "HP:0000975" + ], + "increased sweating": [ + "HP:0000975" + ], + "profuse sweat": [ + "HP:0000975" + ], + "profuse sweating": [ + "HP:0000975" + ], + "sweat": [ + "HP:0000975" + ], + "sweating": [ + "HP:0000975" + ], + "sweat profusely": [ + "HP:0000975" + ], + "sweating profusely": [ + "HP:0000975" + ], + "sweating , increase": [ + "HP:0000975" + ], + "sweating , increased": [ + "HP:0000975" + ], + "eczematoid dermatitis": [ + "HP:0000976" + ], + "soft skin": [ + "HP:0000977" + ], + "velvety skin": [ + "HP:0000977" + ], + "velvety skin texture": [ + "HP:0000977" + ], + "bruise susceptibility": [ + "HP:0000978" + ], + "bruising susceptibility": [ + "HP:0000978" + ], + "bruisability": [ + "HP:0000978" + ], + "bruise easily": [ + "HP:0000978" + ], + "easy bruisability": [ + "HP:0000978" + ], + "easy bruising": [ + "HP:0000978" + ], + "purpura": [ + "HP:0000979" + ], + "blood spot": [ + "HP:0000979" + ], + "blood spots": [ + "HP:0000979" + ], + "red or purple spot on the skin": [ + "HP:0000979" + ], + "red or purple spots on the skin": [ + "HP:0000979" + ], + "pallor": [ + "HP:0000980" + ], + "paleness": [ + "HP:0000980" + ], + "skin paleness": [ + "HP:0000980" + ], + "palmoplantar keratoderma": [ + "HP:0000982" + ], + "palmar and plantar keratoderma": [ + "HP:0000982" + ], + "thickening of palm and sol": [ + "HP:0000982" + ], + "thickening of palms and soles": [ + "HP:0000982" + ], 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pseudotumors": [ + "HP:0000993" + ], + "molluscoid pseudotumor": [ + "HP:0000993" + ], + "melanocytic nevus": [ + "HP:0000995" + ], + "beauty mark": [ + "HP:0000995" + ], + "melanocytic naevus": [ + "HP:0000995" + ], + "melanocytic nevi": [ + "HP:0000995" + ], + "nevocellular nevus": [ + "HP:0000995" + ], + "nevocellular nevi": [ + "HP:0000995" + ], + "noncancerous mole": [ + "HP:0000995" + ], + "pigment naevi": [ + "HP:0000995" + ], + "pigmented naevi": [ + "HP:0000995" + ], + "pigment nevus": [ + "HP:0000995" + ], + "pigmented nevi": [ + "HP:0000995" + ], + "facial capillary hemangioma": [ + "HP:0000996" + ], + "axillary freckling": [ + "HP:0000997" + ], + "hypertrichosis": [ + "HP:0000998" + ], + "excessive hair growth": [ + "HP:0000998" + ], + "increase hair growth on body": [ + "HP:0000998" + ], + "increased hair growth on body": [ + "HP:0000998" + ], + "pyoderma": [ + "HP:0000999" + ], + "pu - fill lesion": [ + "HP:0000999" + ], + "pus - filled lesion": [ + "HP:0000999" + ], + 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"HP:0001010" + ], + "hypopigmentation": [ + "HP:0001010" + ], + "hypopigmented skin": [ + "HP:0001010" + ], + "patchy lighten skin": [ + "HP:0001010" + ], + "patchy lightened skin": [ + "HP:0001010" + ], + "skin hypopigmentation": [ + "HP:0001010" + ], + "obsolete diaphoresis ( with pheochromocytoma )": [ + "HP:0001011" + ], + "multiple lipoma": [ + "HP:0001012" + ], + "multiple lipomas": [ + "HP:0001012" + ], + "lipoma": [ + "HP:0012032" + ], + "lipomas": [ + "HP:0001012" + ], + "lipomatosis": [ + "HP:0001012" + ], + "multiple fatty lump": [ + "HP:0001012" + ], + "multiple fatty lumps": [ + "HP:0001012" + ], + "eruptive xanthoma": [ + "HP:0001013" + ], + "eruptive xanthomas": [ + "HP:0001013" + ], + "angiokeratoma": [ + "HP:0001014" + ], + "angiokeratomas": [ + "HP:0001014" + ], + "prominent superficial vein": [ + "HP:0001015" + ], + "prominent superficial veins": [ + "HP:0001015" + ], + "prominent vein": [ + "HP:0001015" + ], + "prominent veins": [ + "HP:0001015" + ], + "anemic pallor": [ + "HP:0001017" + ], + "anaemic pallor": [ + "HP:0001017" + ], + "abnormal palmar dermatoglyphic": [ + "HP:0001018" + ], + "abnormal palmar dermatoglyphics": [ + "HP:0001018" + ], + "erythroderma": [ + "HP:0001019" + ], + "exfoliative dermititis": [ + "HP:0001019" + ], + "generalise erythroderma": [ + "HP:0001019" + ], + "generalised erythroderma": [ + "HP:0001019" + ], + "generalise erythrodermia": [ + "HP:0001019" + ], + "generalised erythrodermia": [ + "HP:0001019" + ], + "generalize erythroderma": [ + "HP:0001019" + ], + "generalized erythroderma": [ + "HP:0001019" + ], + "generalize erythrodermia": [ + "HP:0001019" + ], + "generalized erythrodermia": [ + "HP:0001019" + ], + "red scaly skin cause by inflammatory skin disease": [ + "HP:0001019" + ], + "red scaly skin caused by inflammatory skin disease": [ + "HP:0001019" + ], + "albinism": [ + "HP:0001022" + ], + "achromasia": [ + "HP:0001022" + ], + "skin dimple over apex of long bone angulation": [ + "HP:0001024" + ], + "urticaria": [ + "HP:0001025" + ], + "hive": [ + "HP:0001025" + ], + "hives": [ + "HP:0001025" + ], + "penetrate foot ulcer": [ + "HP:0001026" + ], + "penetrating foot ulcers": [ + "HP:0001026" + ], + "soft , doughy skin": [ + "HP:0001027" + ], + "hemangioma": [ + "HP:0001028" + ], + "hemangiomata": [ + "HP:0001028" + ], + "strawberry mark": [ + "HP:0001028" + ], + "poikiloderma": [ + "HP:0001029" + ], + "fragile skin": [ + "HP:0001030" + ], + "skin fragility": [ + "HP:0001030" + ], + "subcutaneous lipoma": [ + "HP:0001031" + ], + "absent distal interphalangeal crease": [ + "HP:0001032" + ], + "absent distal interphalangeal creases": [ + "HP:0001032" + ], + "absence of skin crease over distal interphalangeal joint": [ + "HP:0001032" + ], + "absence of skin creases over distal interphalangeal joints": [ + "HP:0001032" + ], + "aplasia of the distal interphalangeal crease": [ + "HP:0001032" + ], + "aplasia of the distal interphalangeal creases": [ + "HP:0001032" + ], + "distal finger flexion crease absent": [ + "HP:0001032" + ], + "distal finger flexion creases absent": [ + "HP:0001032" + ], + "facial flushing after alcohol intake": [ + "HP:0001033" + ], + "hypermelanotic macule": [ + "HP:0001034" + ], + "hyperpigmented macule": [ + "HP:0001034" + ], + "hyperpigmented macules": [ + "HP:0001034" + ], + "hyperpigmented skin patch": [ + "HP:0001034" + ], + "hyperpigmented skin patches": [ + "HP:0001034" + ], + "hyperpigmented spot": [ + "HP:0001034" + ], + "hyperpigmented spots": [ + "HP:0001034" + ], + "parakeratosis": [ + "HP:0001036" + ], + "warfarin - induced skin necrosis": [ + "HP:0001038" + ], + "atheroeruptive xanthoma": [ + "HP:0001039" + ], + "multiple pterygium": [ + "HP:0001040" + ], + "multiple pterygia": [ + "HP:0001040" + ], + "facial erythema": [ + "HP:0001041" + ], + "blush cheek": [ + "HP:0001041" + ], + "blushed cheeks": [ + "HP:0001041" + ], + "blushing": [ + "HP:0001041" + ], + "red face": [ + "HP:0001041" + ], + "red in the face": [ + "HP:0001041" + ], + "rosacea": [ + "HP:0001041" + ], + "ruddy face": [ + "HP:0001041" + ], + "high axial triradius": [ + "HP:0001042" + ], + "prominent scalp vein": [ + "HP:0001043" + ], + "prominent scalp veins": [ + "HP:0001043" + ], + "vitiligo": [ + "HP:0001045" + ], + "blotchy loss of skin color": [ + "HP:0001045" + ], + "blotchy loss of skin colour": [ + "HP:0001045" + ], + "intermittent jaundice": [ + "HP:0001046" + ], + "intermittent icterus": [ + "HP:0001046" + ], + "intermittent yellow skin": [ + "HP:0001046" + ], + "intermittent yellowing of skin": [ + "HP:0001046" + ], + "atopic dermatitis": [ + "HP:0001047" + ], + "atopic dermatitis , chronic": [ + "HP:0001047" + ], + "baby eczema": [ + "HP:0001047" + ], + "dermatitis , atopic": [ + "HP:0001047" + ], + "cavernous hemangioma": [ + "HP:0001048" + ], + "cavernous angioma": [ + "HP:0001048" + ], + "cavernous haemangioma": [ + "HP:0001048" + ], + "collection of dilated blood vessel that form mass": [ + "HP:0001048" + ], + "collection of dilated blood vessels that forms mass": [ + "HP:0001048" + ], + "absent dorsal skin crease over affected joint": [ + "HP:0001049" + ], + "absent dorsal skin creases over affected joints": [ + "HP:0001049" + ], + "plethora": [ + "HP:0001050" + ], + "seborrheic dermatitis": [ + "HP:0001051" + ], + "dysseborrheic dermatitis": [ + "HP:0001051" + ], + "seborrhea": [ + "HP:0001051" + ], + "seborrheic eczema": [ + "HP:0001051" + ], + "nevus flammeus": [ + "HP:0001052" + ], + "nevus simplex": [ + "HP:0001052" + ], + "port - wine stain": [ + "HP:0001052" + ], + "hypopigmented skin patch": [ + "HP:0001053" + ], + "hypopigmented skin patches": [ + "HP:0001053" + ], + "patchy loss of skin color": [ + "HP:0001053" + ], + "patchy loss of skin colour": [ + "HP:0001053" + ], + "numerous nevus": [ + "HP:0001054" + ], + "numerous nevi": [ + "HP:0001054" + ], + "multiple pigment nevus": [ + "HP:0001054" + ], + "multiple pigmented nevi": [ + "HP:0001054" + ], + "numerous mole": [ + "HP:0001054" + ], + "numerous moles": [ + "HP:0001054" + ], + "erysipelas": [ + "HP:0001055" + ], + "st. anthony 's fire": [ + "HP:0001055" + ], + "milium": [ + "HP:0001056" + ], + "milia": [ + "HP:0001056" + ], + "milk spot": [ + "HP:0001056" + ], + "millium cyst": [ + "HP:0001056" + ], + "aplasia cutis congenita": [ + "HP:0001057" + ], + "absence of part of skin at birth": [ + "HP:0001057" + ], + "congenital absence of skin": [ + "HP:0001057" + ], + "congenital scar": [ + "HP:0001057" + ], + "congenital scars": [ + "HP:0001057" + ], + "cutis aplasia": [ + "HP:0001057" + ], + "poor wind heal": [ + "HP:0001058" + ], + "poor wound healing": [ + "HP:0001058" + ], + "pterygium": [ + "HP:0001059" + ], + "pterygia": [ + "HP:0001059" + ], + "surfer 's eye": [ + "HP:0001059" + ], + "axillary pterygium": [ + "HP:0001060" + ], + "axillary pterygia": [ + "HP:0001060" + ], + "acne": [ + "HP:0001061" + ], + "break out": [ + "HP:0001061" + ], + "breaking out": [ + "HP:0001061" + ], + "atypical nevus": [ + "HP:0001062" + ], + "atypical mole": [ + "HP:0001062" + ], + "dysplastic nevus": [ + "HP:0001062" + ], + "acrocyanosis": [ + "HP:0001063" + ], + "persistent blue color of hand or foot": [ + "HP:0001063" + ], + "persistent blue color of hands or feet": [ + "HP:0001063" + ], + "persistent blue colour of hand or foot": [ + "HP:0001063" + ], + "persistent blue colour of hands or feet": [ + "HP:0001063" + ], + "stria distensae": [ + "HP:0001065" + ], + "striae distensae": [ + "HP:0001065" + ], + "purplish stria": [ + "HP:0001065" + ], + "purplish striae": [ + "HP:0001065" + ], + "stretch mark": [ + "HP:0001065" + ], + "stretch marks": [ + "HP:0001065" + ], + "stria": [ + "HP:0001065" + ], + "striae": [ + "HP:0001065" + ], + "stria atrophicae": [ + "HP:0001065" + ], + "striae atrophicae": [ + "HP:0001065" + ], + "stria cutis distensae": [ + "HP:0001065" + ], + "striae cutis distensae": [ + "HP:0001065" + ], + "neurofibroma": [ + "HP:0001067" + ], + "neurofibromas": [ + "HP:0001067" + ], + "multiple neurofibroma": [ + "HP:0001067" + ], + "multiple neurofibromas": [ + "HP:0001067" + ], + "neurofibromata": [ + "HP:0001067" + ], + "neurofibromatosis": [ + "HP:0001067" + ], + "episodic hyperhidrosis": [ + "HP:0001069" + ], + "hyperhidrosis , episodic": [ + "HP:0001069" + ], + "sporadic excessive sweating": [ + "HP:0001069" + ], + "mottle pigmentation": [ + "HP:0001070" + ], + "mottled pigmentation": [ + "HP:0001070" + ], + "mottle skin color": [ + "HP:0001070" + ], + "mottled skin coloring": [ + "HP:0001070" + ], + "mottle skin colour": [ + "HP:0001070" + ], + "mottled skin colouring": [ + "HP:0001070" + ], + "stipple pigmentation": [ + "HP:0001070" + ], + "stippled pigmentation": [ + "HP:0001070" + ], + "angiokeratoma corporis diffusum": [ + "HP:0001071" + ], + "fabry syndrome": [ + "HP:0001071" + ], + "thicken skin": [ + "HP:0001072" + ], + "thickened skin": [ + "HP:0001072" + ], + "diffusely thicken skin": [ + "HP:0001072" + ], + "diffusely thickened skin": [ + "HP:0001072" + ], + "pachydermia": [ + "HP:0001072" + ], + "thick skin": [ + "HP:0001072" + ], + "cigarette - paper scar": [ + "HP:0001073" + ], + "cigarette - paper scars": [ + "HP:0001073" + ], + "'cigarette paper scarring '": [ + "HP:0001073" + ], + "cigarette paper scar": [ + "HP:0001073" + ], + "cigarette paper scarring": [ + "HP:0001073" + ], + "atypical nevus in non - sun expose area": [ + "HP:0001074" + ], + "atypical nevi in non - sun exposed areas": [ + "HP:0001074" + ], + "atrophic scar": [ + "HP:0001075" + ], + "atrophic scars": [ + "HP:0001075" + ], + "sunken or indent skin due to damage": [ + "HP:0001075" + ], + "sunken or indented skin due to damage": [ + "HP:0001075" + ], + "thin , atrophic scar": [ + "HP:0001075" + ], + "thin , atrophic scars": [ + "HP:0001075" + ], + "glabellar hemangioma": [ + "HP:0001076" + ], + "glabellar capillary hemangioma": [ + "HP:0001076" + ], + "biliary tract abnormality": [ + "HP:0001080" + ], + "biliary tract disease": [ + "HP:0001080" + ], + "cholelithiasis": [ + "HP:0001081" + ], + "gallstone": [ + "HP:0001081" + ], + "gallstones": [ + "HP:0001081" + ], + "cholecystitis": [ + "HP:0001082" + ], + "gallbladder inflammation": [ + "HP:0001082" + ], + "ectopia lentis": [ + "HP:0001083" + ], + "abnormality of lens position": [ + "HP:0001083" + ], + "lens dislocation": [ + "HP:0001083" + ], + "corneal arcus": [ + "HP:0001084" + ], + "anterior embryotoxon": [ + "HP:0001084" + ], + "arcus juvenilis": [ + "HP:0001084" + ], + "arcus lipoidis": [ + "HP:0001084" + ], + "arcus senilis": [ + "HP:0001084" + ], + "corneal annulus": [ + "HP:0001084" + ], + "gerontoxon": [ + "HP:0001084" + ], + "papilledema": [ + "HP:0001085" + ], + "developmental glaucoma": [ + "HP:0001087" + ], + "childhood glaucoma": [ + "HP:0001087" + ], + "infantile glaucoma": [ + "HP:0001087" + ], + "paediatric glaucoma": [ + "HP:0001087" + ], + "pediatric glaucoma": [ + "HP:0001087" + ], + "brushfield spot": [ + "HP:0001088" + ], + "brushfield spots": [ + "HP:0001088" + ], + "iris brushfield spot": [ + "HP:0001088" + ], + "iris brushfield spots": [ + "HP:0001088" + ], + "speckle iris": [ + "HP:0001088" + ], + "speckled iris": [ + "HP:0001088" + ], + "iris atrophy": [ + "HP:0001089" + ], + "iris degeneration": [ + "HP:0001089" + ], + "abnormally large globe": [ + "HP:0001090" + ], + "increase size of eye": [ + "HP:0001090" + ], + "increased size of eyes": [ + "HP:0001090" + ], + "increase size of palpebral fissure": [ + "HP:0001090" + ], + "increased size of palpebral fissures": [ + "HP:0001090" + ], + "large eyeball": [ + "HP:0001090" + ], + "large eyeballs": [ + "HP:0001090" + ], + "large eye": [ + "HP:0001090" + ], + "large eyes": [ + "HP:0001090" + ], + "large of palpebral fissure": [ + "HP:0001090" + ], + "large of palpebral fissures": [ + "HP:0001090" + ], + "megalophthalmos": [ + "HP:0001090" + ], + "absent lacrimal punctum": [ + "HP:0001092" + ], + "absent lacrimal gland puncta": [ + "HP:0001092" + ], + "absent lacrimal opening": [ + "HP:0001092" + ], + "absent lacrimal openings": [ + "HP:0001092" + ], + "absent lacrimal puncta": [ + "HP:0001092" + ], + "agenesis of the lacrimal punctum": [ + "HP:0001092" + ], + "aplasia of lacrimal puncta": [ + "HP:0001092" + ], + "lacrimal puncta aplasia": [ + "HP:0001092" + ], + "lacrimal punctum , absence": [ + "HP:0001092" + ], + "optic nerve dysplasia": [ + "HP:0001093" + ], + "iridocyclitis": [ + "HP:0001094" + ], + "hypertensive retinopathy": [ + "HP:0001095" + ], + "keratoconjunctivitis": [ + "HP:0001096" + ], + "keratoconjunctivitis sicca": [ + "HP:0001097" + ], + "dry eye syndrome": [ + "HP:0001097" + ], + "dry eye": [ + "HP:0001097" + ], + "dry eyes": [ + "HP:0001097" + ], + "keratitis sicca": [ + "HP:0001097" + ], + "xerophthalmia": [ + "HP:0001097" + ], + "abnormal fundus morphology": [ + "HP:0001098" + ], + "abnormality of the fundus": [ + "HP:0001098" + ], + "fundus atrophy": [ + "HP:0001099" + ], + "heterochromia iridis": [ + "HP:0001100" + ], + "different color eye": [ + "HP:0001100" + ], + "different colored eyes": [ + "HP:0001100" + ], + "different colour eye": [ + "HP:0001100" + ], + "different coloured eyes": [ + "HP:0001100" + ], + "heterochromia iris": [ + "HP:0001100" + ], + "heterochromia irides": [ + "HP:0001100" + ], + "iritis": [ + "HP:0001101" + ], + "inflammation of iris": [ + "HP:0001101" + ], + "angioid streak of the fundus": [ + "HP:0001102" + ], + "angioid streaks of the fundus": [ + "HP:0001102" + ], + "angioid streak": [ + "HP:0001102" + ], + "angioid streaks": [ + "HP:0001102" + ], + "angioid streak of the retina": [ + "HP:0001102" + ], + "angioid streaks of the retina": [ + "HP:0001102" + ], + "angioid streak , retina": [ + "HP:0001102" + ], + "angioid streaks , retina": [ + "HP:0001102" + ], + "knapp streak": [ + "HP:0001102" + ], + "knapp streaks": [ + "HP:0001102" + ], + "laquer crack of the retina": [ + "HP:0001102" + ], + "laquer cracks of the retina": [ + "HP:0001102" + ], + "abnormal macular morphology": [ + "HP:0001103" + ], + "abnormality of the macula": [ + "HP:0001103" + ], + "macula abnormality": [ + "HP:0001103" + ], + "macular abnormality": [ + "HP:0001103" + ], + "macular hypoplasia": [ + "HP:0001104" + ], + "retinal atrophy": [ + "HP:0001105" + ], + "periorbital hyperpigmentation": [ + "HP:0001106" + ], + "dark circle around the eye": [ + "HP:0001106" + ], + "dark circles around the eyes": [ + "HP:0001106" + ], + "dark circle under the eye": [ + "HP:0001106" + ], + "dark circles under the eyes": [ + "HP:0001106" + ], + "darken around the eye": [ + "HP:0001106" + ], + "darkening around the eyes": [ + "HP:0001106" + ], + "idiopathic cutaneous hyperchromia at the orbital region": [ + "HP:0001106" + ], + "infraorbital pigmentation": [ + "HP:0001106" + ], + "periorbital melanosis": [ + "HP:0001106" + ], + "pigmentation around the eye": [ + "HP:0001106" + ], + "pigmentation around the eyes": [ + "HP:0001106" + ], + "ocular albinism": [ + "HP:0001107" + ], + "absent pigmentation in the eye": [ + "HP:0001107" + ], + "albinism , ocular": [ + "HP:0001107" + ], + "leber optic atrophy": [ + "HP:0001112" + ], + "leber optic atrophy feature": [ + "HP:0001112" + ], + "leber optic atrophy features": [ + "HP:0001112" + ], + "leber optic degeneration": [ + "HP:0001112" + ], + "obsolete early cataract": [ + "HP:0001113" + ], + "obsolete early cataracts": [ + "HP:0001113" + ], + "xanthelasma": [ + "HP:0001114" + ], + "fatty deposit in skin around the eye": [ + "HP:0001114" + ], + "fatty deposits in skin around the eyes": [ + "HP:0001114" + ], + "fatty deposit on eyelid": [ + "HP:0001114" + ], + "fatty deposits on eyelids": [ + "HP:0001114" + ], + "xanthelasma of eyelid": [ + "HP:0001114" + ], + "xanthelasma of periocular region": [ + "HP:0001114" + ], + "xanthelasma palpebrarum": [ + "HP:0001114" + ], + "xanthoma": [ + "HP:0001114" + ], + "xanthoma of eyelid": [ + "HP:0001114" + ], + "xanthoma of periocular region": [ + "HP:0001114" + ], + "posterior polar cataract": [ + "HP:0001115" + ], + "polar cataract , posterior": [ + "HP:0001115" + ], + "macular coloboma": [ + "HP:0001116" + ], + "coloboma of the macula": [ + "HP:0001116" + ], + "sudden loss of visual acuity": [ + "HP:0001117" + ], + "sudden central visual loss": [ + "HP:0001117" + ], + "sudden decrease in vision": [ + "HP:0001117" + ], + "juvenile cataract": [ + "HP:0001118" + ], + "keratoglobus": [ + "HP:0001119" + ], + "abnormality of corneal size": [ + "HP:0001120" + ], + "obsolete aplasia / hypoplasia of the choroid": [ + "HP:0001122" + ], + "visual field defect": [ + "HP:0001123" + ], + "partial loss of field of vision": [ + "HP:0001123" + ], + "visual field defects": [ + "HP:0001123" + ], + "transient unilateral blurring of vision": [ + "HP:0001125" + ], + "hemianopic blurring": [ + "HP:0001125" + ], + "hemianoptic blurring of vision": [ + "HP:0001125" + ], + "transient unilateral blur vision": [ + "HP:0001125" + ], + "transient unilateral blurred vision": [ + "HP:0001125" + ], + "cryptophthalmos": [ + "HP:0001126" + ], + "trichiasis": [ + "HP:0001128" + ], + "ingrown eyelash": [ + "HP:0001128" + ], + "ingrown eyelashes": [ + "HP:0001128" + ], + "introversion of eyelash": [ + "HP:0001128" + ], + "introversion of eyelashes": [ + "HP:0001128" + ], + "trichiasis of eyelid eyelash": [ + "HP:0001128" + ], + "trichiasis of eyelid eyelashes": [ + "HP:0001128" + ], + "large central visual field defect": [ + "HP:0001129" + ], + "large central loss of field of vision": [ + "HP:0001129" + ], + "corneal dystrophy": [ + "HP:0001131" + ], + "lens subluxation": [ + "HP:0001132" + ], + "partially dislocate lens": [ + "HP:0001132" + ], + "partially dislocated lens": [ + "HP:0001132" + ], + "constriction of peripheral visual field": [ + "HP:0001133" + ], + "concentric narrowing of visual field": [ + "HP:0001133" + ], + "constrict visual field": [ + "HP:0001133" + ], + "constricted visual field": [ + "HP:0001133" + ], + "constricted visual fields": [ + "HP:0001133" + ], + "limited peripheral vision": [ + "HP:0001133" + ], + "visual field constriction": [ + "HP:0001133" + ], + "anterior polar cataract": [ + "HP:0001134" + ], + "polar cataract , anterior": [ + "HP:0001134" + ], + "chorioretinal dystrophy": [ + "HP:0001135" + ], + "retinal arteriolar tortuosity": [ + "HP:0001136" + ], + "tortuous retinal arteriole": [ + "HP:0001136" + ], + "tortuous retinal arterioles": [ + "HP:0001136" + ], + "alternate esotropia": [ + "HP:0001137" + ], + "alternating esotropia": [ + "HP:0001137" + ], + "alternate cross eye": [ + "HP:0001137" + ], + "alternating cross eyes": [ + "HP:0001137" + ], + "optic neuropathy": [ + "HP:0001138" + ], + "damage optic nerve": [ + "HP:0001138" + ], + "damaged optic nerve": [ + "HP:0001138" + ], + "choroideremia": [ + "HP:0001139" + ], + "limbal dermoid": [ + "HP:0001140" + ], + "benign eye tumor": [ + "HP:0001140" + ], + "benign eye tumour": [ + "HP:0001140" + ], + "epibulbar dermoid": [ + "HP:0001140" + ], + "epibulbar dermoids": [ + "HP:0001140" + ], + "severely reduce visual acuity": [ + "HP:0001141" + ], + "severely reduced visual acuity": [ + "HP:0001141" + ], + "mark vision impairment": [ + "HP:0001141" + ], + "marked vision impairment": [ + "HP:0001141" + ], + "severe reduction in visual acuity": [ + "HP:0001141" + ], + "severe vision loss": [ + "HP:0001141" + ], + "severe visual impairment": [ + "HP:0001141" + ], + "severe visual loss": [ + "HP:0001141" + ], + "severely impaired vision": [ + "HP:0001141" + ], + "lenticonus": [ + "HP:0001142" + ], + "orbital cyst": [ + "HP:0001144" + ], + "cyst of eye socket": [ + "HP:0001144" + ], + "orbital cysts": [ + "HP:0001144" + ], + "obsolete chorioretinopathy": [ + "HP:0001145" + ], + "obsolete pigmentary retinal degeneration": [ + "HP:0001146" + ], + "retinal exudate": [ + "HP:0001147" + ], + "retinal exudates": [ + "HP:0001147" + ], + "lattice corneal dystrophy": [ + "HP:0001149" + ], + "biber haab dimmer dystrophy": [ + "HP:0001149" + ], + "obsolete choroidal sclerosis": [ + "HP:0001150" + ], + "impaired horizontal smooth pursuit": [ + "HP:0001151" + ], + "abnormal horizontal ocular pursuit": [ + "HP:0001151" + ], + "impaired horizontal visual pursuit": [ + "HP:0001151" + ], + "saccadic smooth pursuit": [ + "HP:0001152" + ], + "saccadic pursuit movement": [ + "HP:0001152" + ], + "saccadic pursuit movements": [ + "HP:0001152" + ], + "saccadic slow pursuit": [ + "HP:0001152" + ], + "septate vagina": [ + "HP:0001153" + ], + "double vagina": [ + "HP:0001153" + ], + "abnormality of the hand": [ + "HP:0001155" + ], + "abnormal hand": [ + "HP:0001155" + ], + "abnormal hands": [ + "HP:0001155" + ], + "hand anomaly": [ + "HP:0001155" + ], + "hand anomalies": [ + "HP:0001155" + ], + "hand deformity": [ + "HP:0001155" + ], + "hand deformities": [ + "HP:0001155" + ], + "brachydactyly": [ + "HP:0001156" + ], + "brachydactyly syndrome": [ + "HP:0001156" + ], + "short finger or toe": [ + "HP:0001156" + ], + "short fingers or toes": [ + "HP:0001156" + ], + "syndactyly": [ + "HP:0001159" + ], + "webbed finger or toe": [ + "HP:0001159" + ], + "webbed fingers or toes": [ + "HP:0001159" + ], + "hand polydactyly": [ + "HP:0001161" + ], + "extra finger": [ + "HP:0001161" + ], + "finger polydactyly": [ + "HP:0001161" + ], + "polydactyly of the hand": [ + "HP:0001161" + ], + "supernumerary finger": [ + "HP:0001161" + ], + "postaxial hand polydactyly": [ + "HP:0001162" + ], + "extra little finger": [ + "HP:0001162" + ], + "extra pinkie finger": [ + "HP:0001162" + ], + "extra pinky finger": [ + "HP:0001162" + ], + "polydactyly affect the 5th finger": [ + "HP:0001162" + ], + "polydactyly affecting the 5th finger": [ + "HP:0001162" + ], + "postaxial polydactyly of finger": [ + "HP:0001162" + ], + "postaxial polydactyly of fingers": [ + "HP:0001162" + ], + "postaxial polydactyly of hand": [ + "HP:0001162" + ], + "postaxial polydactyly of hands": [ + "HP:0001162" + ], + "abnormality of the metacarpal bone": [ + "HP:0001163" + ], + "abnormality of the metacarpal bones": [ + "HP:0001163" + ], + "abnormality of the long bone of hand": [ + "HP:0001163" + ], + "anomaly of the metacarpal bone": [ + "HP:0001163" + ], + "anomaly of the metacarpal bones": [ + "HP:0001163" + ], + "arachnodactyly": [ + "HP:0001166" + ], + "long slender finger": [ + "HP:0001166" + ], + "long slender fingers": [ + "HP:0001166" + ], + "long , slender finger": [ + "HP:0001166" + ], + "long , slender fingers": [ + "HP:0001166" + ], + "spider finger": [ + "HP:0001166" + ], + "spider fingers": [ + "HP:0001166" + ], + "abnormality of finger": [ + "HP:0001167" + ], + "abnormality of the finger": [ + "HP:0001167" + ], + "abnormalities of the fingers": [ + "HP:0001167" + ], + "broad palm": [ + "HP:0001169" + ], + "broad hand": [ + "HP:0001169" + ], + "broad hands": [ + "HP:0001169" + ], + "wide palm": [ + "HP:0001169" + ], + "split hand": [ + "HP:0001171" + ], + "claw hand": [ + "HP:0001171" + ], + "claw hand deformity": [ + "HP:0001171" + ], + "claw hand deformities": [ + "HP:0001171" + ], + "claw hands": [ + "HP:0001171" + ], + "claw - hand deformity": [ + "HP:0001171" + ], + "claw - hand deformities": [ + "HP:0001171" + ], + "ectrodactyly of the hand": [ + "HP:0001171" + ], + "hand ectrodactyly": [ + "HP:0001171" + ], + "split - hand": [ + "HP:0001171" + ], + "abnormal thumb morphology": [ + "HP:0001172" + ], + "abnormality of the thumb": [ + "HP:0001172" + ], + "abnormality of the thumbs": [ + "HP:0001172" + ], + "thumb deformity": [ + "HP:0001172" + ], + "large hand": [ + "HP:0001176" + ], + "large hands": [ + "HP:0001176" + ], + "disproportionately large hand": [ + "HP:0001176" + ], + "disproportionately large hands": [ + "HP:0001176" + ], + "preaxial hand polydactyly": [ + "HP:0001177" + ], + "extra thumb": [ + "HP:0001177" + ], + "polydactyly affect the thumb": [ + "HP:0001177" + ], + "polydactyly affecting the thumb": [ + "HP:0001177" + ], + "preaxial polydactyly of hand": [ + "HP:0001177" + ], + "preaxial polydactyly of hands": [ + "HP:0001177" + ], + "supernumerary thumb": [ + "HP:0001177" + ], + "thumb polydactyly": [ + "HP:0001177" + ], + "ulnar claw": [ + "HP:0001178" + ], + "hand oligodactyly": [ + "HP:0001180" + ], + "hand have less than 5 finger": [ + "HP:0001180" + ], + "hand has less than 5 fingers": [ + "HP:0001180" + ], + "adduct thumb": [ + "HP:0001181" + ], + "adducted thumb": [ + "HP:0001181" + ], + "adducted thumbs": [ + "HP:0001181" + ], + "inward turn thumb": [ + "HP:0001181" + ], + "inward turned thumb": [ + "HP:0001181" + ], + "taper finger": [ + "HP:0001182" + ], + "tapered finger": [ + "HP:0001182" + ], + "distally taper finger": [ + "HP:0001182" + ], + "distally tapering fingers": [ + "HP:0001182" + ], + "tapered fingers": [ + "HP:0001182" + ], + "taper fingertip": [ + "HP:0001182" + ], + "tapered fingertips": [ + "HP:0001182" + ], + "tapering fingers": [ + "HP:0001182" + ], + "hyperextensibility of the finger joint": [ + "HP:0001187" + ], + "hyperextensibility of the finger joints": [ + "HP:0001187" + ], + "finger joint hyperextensibility": [ + "HP:0001187" + ], + "hyperextensible digit": [ + "HP:0001187" + ], + "hyperextensible digits": [ + "HP:0001187" + ], + "hyperextensible finger": [ + "HP:0001187" + ], + "hyperextensible fingers": [ + "HP:0001187" + ], + "hand clench": [ + "HP:0001188" + ], + "hand clenching": [ + "HP:0001188" + ], + "clench hand": [ + "HP:0001188" + ], + "clenched hands": [ + "HP:0001188" + ], + "abnormality of the carpal bone": [ + "HP:0001191" + ], + "abnormality of the carpal bones": [ + "HP:0001191" + ], + "abnormal carpal bone": [ + "HP:0001191" + ], + "abnormal carpal bones": [ + "HP:0001191" + ], + "abnormal wrist bone": [ + "HP:0001191" + ], + "abnormal wrist bones": [ + "HP:0001191" + ], + "anomalous carpal bone": [ + "HP:0001191" + ], + "anomalous carpal bones": [ + "HP:0001191" + ], + "carpal bone anomaly": [ + "HP:0001191" + ], + "carpal bone anomalies": [ + "HP:0001191" + ], + "ulnar deviation of the hand or of finger of the hand": [ + "HP:0001193" + ], + "ulnar deviation of the hand or of fingers of the hand": [ + "HP:0001193" + ], + "abnormality of placenta or umbilical cord": [ + "HP:0001194" + ], + "abnormalities of placenta or umbilical cord": [ + "HP:0001194" + ], + "single umbilical artery": [ + "HP:0001195" + ], + "2 vessel cord": [ + "HP:0001195" + ], + "2 vessel umbilical cord": [ + "HP:0001195" + ], + "only one artery in umbilical cord instead of two": [ + "HP:0001195" + ], + "two vessel cord": [ + "HP:0001195" + ], + "two vessel umbilical cord": [ + "HP:0001195" + ], + "two - vessel cord": [ + "HP:0001195" + ], + "short umbilical cord": [ + "HP:0001196" + ], + "abnormality of prenatal development or birth": [ + "HP:0001197" + ], + "triphalangeal thumb": [ + "HP:0001199" + ], + "accessory phalanx of the thumb": [ + "HP:0001199" + ], + "digitalize thumb": [ + "HP:0001199" + ], + "digitalized thumb": [ + "HP:0001199" + ], + "finger - like thumb": [ + "HP:0001199" + ], + "triphalangeal thumbs": [ + "HP:0001199" + ], + "triphalangy of thumb": [ + "HP:0001199" + ], + "distal symphalangism of hand": [ + "HP:0001204" + ], + "distal symphalangism of hands": [ + "HP:0001204" + ], + "fuse outermost bone of hand": [ + "HP:0001204" + ], + "fused outermost bones of hand": [ + "HP:0001204" + ], + "symphalangism affect the distal phalanx of the hand": [ + "HP:0001204" + ], + "symphalangism affecting the distal phalanges of the hand": [ + "HP:0001204" + ], + "synostosis of distal phalanx": [ + "HP:0001204" + ], + "synostosis of distal phalanges": [ + "HP:0001204" + ], + "terminal symphalangism": [ + "HP:0001204" + ], + "abnormal fingertip morphology": [ + "HP:0001211" + ], + "abnormality of the fingertip": [ + "HP:0001211" + ], + "abnormality of the fingertips": [ + "HP:0001211" + ], + "prominent fingertip pad": [ + "HP:0001212" + ], + "prominent fingertip pads": [ + "HP:0001212" + ], + "persistence of fingerpads": [ + "HP:0001212" + ], + "persistent fetal fingertip pad": [ + "HP:0001212" + ], + "persistent fetal fingertip pads": [ + "HP:0001212" + ], + "persistent foetal fingertip pad": [ + "HP:0001212" + ], + "persistent foetal fingertip pads": [ + "HP:0001212" + ], + "prominent finger pad": [ + "HP:0001212" + ], + "prominent finger pads": [ + "HP:0001212" + ], + "camptodactyly of 2nd - 5th finger": [ + "HP:0001215" + ], + "camptodactyly of 2nd - 5th fingers": [ + "HP:0001215" + ], + "delay ossification of carpal bone": [ + "HP:0001216" + ], + "delayed ossification of carpal bones": [ + "HP:0001216" + ], + "carpal delay ossification": [ + "HP:0001216" + ], + "carpal delayed ossification": [ + "HP:0001216" + ], + "delay carpal bone age": [ + "HP:0001216" + ], + "delayed carpal bone age": [ + "HP:0001216" + ], + "delay carpal ossification": [ + "HP:0001216" + ], + "delayed carpal ossification": [ + "HP:0001216" + ], + "delay maturation of carpal bone": [ + "HP:0001216" + ], + "delayed maturation of carpal bones": [ + "HP:0001216" + ], + "delay maturation of wrist bone": [ + "HP:0001216" + ], + "delayed maturation of wrist bone": [ + "HP:0001216" + ], + "club": [ + "HP:0001217" + ], + "clubbing": [ + "HP:0001217" + ], + "clubbing of finger and toe": [ + "HP:0001217" + ], + "clubbing of fingers and toes": [ + "HP:0001217" + ], + "digital clubbing": [ + "HP:0001217" + ], + "autoamputation": [ + "HP:0001218" + ], + "interphalangeal joint contracture of finger": [ + "HP:0001220" + ], + "interphalangeal joint flexion contracture": [ + "HP:0001220" + ], + "interphalangeal joint flexion contractures": [ + "HP:0001220" + ], + "spatulate thumb": [ + "HP:0001222" + ], + "spatulate thumbs": [ + "HP:0001222" + ], + "spoon shape thumb": [ + "HP:0001222" + ], + "spoon shaped thumbs": [ + "HP:0001222" + ], + "point proximal second through fifth metacarpal": [ + "HP:0001223" + ], + "pointed proximal second through fifth metacarpals": [ + "HP:0001223" + ], + "wrist swell": [ + "HP:0001225" + ], + "wrist swelling": [ + "HP:0001225" + ], + "obsolete acral ulceration and osteomyelitis lead to autoamputation of digit": [ + "HP:0001226" + ], + "obsolete acral ulceration and osteomyelitis leading to autoamputation of digits": [ + "HP:0001226" + ], + "abnormality of the thenar eminence": [ + "HP:0001227" + ], + "thenar abnormality": [ + "HP:0001227" + ], + "broad metacarpal": [ + "HP:0001230" + ], + "broad metacarpals": [ + "HP:0001230" + ], + "wide long bone of hand": [ + "HP:0001230" + ], + "wide long bones of hand": [ + "HP:0001230" + ], + "wide metacarpal": [ + "HP:0001230" + ], + "wide metacarpals": [ + "HP:0001230" + ], + "abnormal fingernail morphology": [ + "HP:0001231" + ], + "abnormal fingernail": [ + "HP:0001231" + ], + "abnormal fingernails": [ + "HP:0001231" + ], + "abnormality of the fingernail": [ + "HP:0001231" + ], + "abnormality of the fingernails": [ + "HP:0001231" + ], + "nail bed telangiectasia": [ + "HP:0001232" + ], + "nail bed telangiectases": [ + "HP:0001232" + ], + "2 - 3 finger syndactyly": [ + "HP:0001233" + ], + "syndactyly 2nd - 3rd finger": [ + "HP:0001233" + ], + "syndactyly 2nd - 3rd fingers": [ + "HP:0001233" + ], + "syndactyly , 2 - 3 finger": [ + "HP:0001233" + ], + "web 2nd - 3rd finger": [ + "HP:0001233" + ], + "webbed 2nd - 3rd fingers": [ + "HP:0001233" + ], + "hitchhiker thumb": [ + "HP:0001234" + ], + "abduct thumb": [ + "HP:0001234" + ], + "abducted thumb": [ + "HP:0001234" + ], + "slender finger": [ + "HP:0001238" + ], + "narrow finger": [ + "HP:0001238" + ], + "narrow fingers": [ + "HP:0001238" + ], + "slender fingers": [ + "HP:0001238" + ], + "thin finger": [ + "HP:0001238" + ], + "thin fingers": [ + "HP:0001238" + ], + "wrist flexion contracture": [ + "HP:0001239" + ], + "wrist contracture": [ + "HP:0001239" + ], + "wrist flexion deformity": [ + "HP:0001239" + ], + "capitate - hamate fusion": [ + "HP:0001241" + ], + "capitate - hamate fusions": [ + "HP:0001241" + ], + "fuse capitate and hamate": [ + "HP:0001241" + ], + "fused capitate and hamate": [ + "HP:0001241" + ], + "fusion of capitate and hamate": [ + "HP:0001241" + ], + "fusion of hamate and capitate": [ + "HP:0001241" + ], + "small thenar eminence": [ + "HP:0001245" + ], + "decrease thenar eminence": [ + "HP:0001245" + ], + "decreased thenar eminence": [ + "HP:0001245" + ], + "hypoplastic thenar eminence": [ + "HP:0001245" + ], + "hypoplastic thenar eminences": [ + "HP:0001245" + ], + "thenar hypoplasia": [ + "HP:0001245" + ], + "thenar muscle hypoplasia": [ + "HP:0001245" + ], + "short tubular bone of the hand": [ + "HP:0001248" + ], + "short tubular bones of the hand": [ + "HP:0001248" + ], + "shorten short tubular bone of the hand": [ + "HP:0001248" + ], + "shortened short tubular bones of the hand": [ + "HP:0001248" + ], + "intellectual disability": [ + "HP:0001249" + ], + "dull intelligence": [ + "HP:0001249" + ], + "low intelligence": [ + "HP:0001249" + ], + "mental deficiency": [ + "HP:0001249" + ], + "mental retardation": [ + "HP:0001249" + ], + "mental retardation , nonspecific": [ + "HP:0001249" + ], + "mental - retardation": [ + "HP:0001249" + ], + "nonprogressive intellectual disability": [ + "HP:0001249" + ], + "nonprogressive mental retardation": [ + "HP:0001249" + ], + "poor school performance": [ + "HP:0001249" + ], + "seizure": [ + "HP:0001250" + ], + "epilepsy": [ + "HP:0001250" + ], + "epileptic seizure": [ + "HP:0001250" + ], + "seizures": [ + "HP:0001250" + ], + "ataxia": [ + "HP:0001251" + ], + "cerebellar ataxia": [ + "HP:0001251" + ], + "hypotonia": [ + "HP:0001252" + ], + "central hypotonia": [ + "HP:0001252" + ], + "low muscle tone": [ + "HP:0001252" + ], + "low or weak muscle tone": [ + "HP:0001252" + ], + "muscle hypotonia": [ + "HP:0001252" + ], + "muscular hypotonia": [ + "HP:0001252" + ], + "peripheral hypotonia": [ + "HP:0001252" + ], + "lethargy": [ + "HP:0001254" + ], + "intellectual disability , mild": [ + "HP:0001256" + ], + "mental retardation , borderline - mild": [ + "HP:0001256" + ], + "mental retardation , mild": [ + "HP:0001256" + ], + "mild and nonprogressive mental retardation": [ + "HP:0001256" + ], + "mild mental retardation": [ + "HP:0001256" + ], + "spasticity": [ + "HP:0001257" + ], + "involuntary muscle stiffness , contraction , or spasm": [ + "HP:0001257" + ], + "muscle spasticity": [ + "HP:0001257" + ], + "muscular spasticity": [ + "HP:0001257" + ], + "spastic paraplegia": [ + "HP:0001258" + ], + "spastic paraplegia , low limb": [ + "HP:0001258" + ], + "spastic paraplegia , lower limb": [ + "HP:0001258" + ], + "coma": [ + "HP:0001259" + ], + "dysarthria": [ + "HP:0001260" + ], + "difficulty articulate speech": [ + "HP:0001260" + ], + "difficulty articulating speech": [ + "HP:0001260" + ], + "dysarthric speech": [ + "HP:0001260" + ], + "excessive daytime somnolence": [ + "HP:0001262" + ], + "excessive daytime sleepiness": [ + "HP:0001262" + ], + "more than typical sleepiness during day": [ + "HP:0001262" + ], + "global developmental delay": [ + "HP:0001263" + ], + "cognitive delay": [ + "HP:0001263" + ], + "delay 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hip since birth": [ + "HP:0001374" + ], + "limitation of joint mobility": [ + "HP:0001376" + ], + "decrease joint mobility": [ + "HP:0001376" + ], + "decreased joint mobility": [ + "HP:0001376" + ], + "decreased mobility of joint": [ + "HP:0001376" + ], + "decreased mobility of joints": [ + "HP:0001376" + ], + "limited joint mobility": [ + "HP:0001376" + ], + "limited joint motion": [ + "HP:0001376" + ], + "limited elbow extension": [ + "HP:0001377" + ], + "decrease elbow extension": [ + "HP:0001377" + ], + "decreased elbow extension": [ + "HP:0001377" + ], + "elbow limited extension": [ + "HP:0001377" + ], + "limitation of elbow extension": [ + "HP:0001377" + ], + "limited extension at elbow": [ + "HP:0001377" + ], + "limited extension at elbows": [ + "HP:0001377" + ], + "limited forearm extension": [ + "HP:0001377" + ], + "restrict elbow extension": [ + "HP:0001377" + ], + "restricted elbow extension": [ + "HP:0001377" + ], + "obsolete degenerative joint disease": [ + "HP:0001379" + ], + "obsolete ligamentous laxity": [ + "HP:0001380" + ], + "joint hypermobility": [ + "HP:0001382" + ], + "double - joint": [ + "HP:0001382" + ], + "double - jointed": [ + "HP:0001382" + ], + "extensible joint": [ + "HP:0001382" + ], + "extensible joints": [ + "HP:0001382" + ], + "flexible joint": [ + "HP:0001382" + ], + "flexible joints": [ + "HP:0001382" + ], + "hyperextensible joint": [ + "HP:0001382" + ], + "hyperextensible joints": [ + "HP:0001382" + ], + "increase joint mobility": [ + "HP:0001382" + ], + "increased joint mobility": [ + "HP:0001382" + ], + "increase mobility of joint": [ + "HP:0001382" + ], + "increased mobility of joints": [ + "HP:0001382" + ], + "joint hyperextensibility": [ + "HP:0001382" + ], + "abnormal hip joint morphology": [ + "HP:0001384" + ], + "abnormality of the hip joint": [ + "HP:0001384" + ], + "abnormality of the hip joints": [ + "HP:0001384" + ], + "hip dysplasia": [ + "HP:0001385" + ], + "abnormal formation of the hip": [ + "HP:0001385" + ], + "congenital hip dysplasia": [ + "HP:0001385" + ], + "joint swell": [ + "HP:0001386" + ], + "joint swelling": [ + "HP:0001386" + ], + "joint stiffness": [ + "HP:0001387" + ], + "stiff joint": [ + "HP:0001387" + ], + "stiff joints": [ + "HP:0001387" + ], + "joint laxity": [ + "HP:0001388" + ], + "hyperlaxity": [ + "HP:0001388" + ], + "joint instability": [ + "HP:0001388" + ], + "joint ligamentous laxity": [ + "HP:0001388" + ], + "lax joint": [ + "HP:0001388" + ], + "lax joints": [ + "HP:0001388" + ], + "ligamentous laxity": [ + "HP:0001388" + ], + "loose - jointedness": [ + "HP:0001388" + ], + "loosejointedness": [ + "HP:0001388" + ], + "abnormality of the liver": [ + "HP:0001392" + ], + "abnormal liver": [ + "HP:0001392" + ], + "liver abnormality": [ + "HP:0001392" + ], + "liver disease": [ + "HP:0001392" + ], + "cirrhosis": [ + "HP:0001394" + ], + "hepatic cirrhosis": [ + "HP:0001394" + ], + "liver cirrhosis": [ + "HP:0001394" + ], + "scar tissue replace healthy tissue in the liver": [ + "HP:0001394" + ], + "scar tissue replaces healthy tissue in the liver": [ + "HP:0001394" + ], + "hepatic fibrosis": [ + "HP:0001395" + ], + "liver fibrosis": [ + "HP:0001395" + ], + "cholestasis": [ + "HP:0001396" + ], + "slow or block flow of bile from liver": [ + "HP:0001396" + ], + "slowed or blocked flow of bile from liver": [ + "HP:0001396" + ], + "hepatic steatosis": [ + "HP:0001397" + ], + "fatty infiltration of liver": [ + "HP:0001397" + ], + "fatty liver": [ + "HP:0001397" + ], + "liver steatosis": [ + "HP:0001397" + ], + "steatosis": [ + "HP:0001397" + ], + "hepatic failure": [ + "HP:0001399" + ], + "liver failure": [ + "HP:0001399" + ], + "obsolete hepatic abscess due to immunodeficiency": [ + "HP:0001400" + ], + "obsolete hepatic abscesses due to immunodeficiency": [ + "HP:0001400" + ], + "intrahepatic biliary dysgenesis": [ + "HP:0001401" + ], + "hepatocellular carcinoma": [ + "HP:0001402" + ], + "increase hepatocellular carcinoma risk": [ + "HP:0001402" + ], + "increased hepatocellular carcinoma risk": [ + "HP:0001402" + ], + "increase incidence of hepatocellular carcinoma": [ + "HP:0001402" + ], + "increased incidence of hepatocellular carcinoma": [ + "HP:0001402" + ], + "macrovesicular hepatic steatosis": [ + "HP:0001403" + ], + "macrovesicular steatosis": [ + "HP:0001403" + ], + "hepatocellular necrosis": [ + "HP:0001404" + ], + "death of liver cell": [ + "HP:0001404" + ], + "death of liver cells": [ + "HP:0001404" + ], + "hepatocellular loss": [ + "HP:0001404" + ], + "periportal fibrosis": [ + "HP:0001405" + ], + "intrahepatic cholestasis": [ + "HP:0001406" + ], + "impaired release of bile from liver": [ + "HP:0001406" + ], + "hepatic cyst": [ + "HP:0001407" + ], + "hepatic cysts": [ + "HP:0001407" + ], + "liver cyst": [ + "HP:0001407" + ], + "liver cysts": [ + "HP:0001407" + ], + "bile duct proliferation": [ + "HP:0001408" + ], + "proliferation of bile canaliculus": [ + "HP:0001408" + ], + "proliferation of bile canaliculi": [ + "HP:0001408" + ], + "portal hypertension": [ + "HP:0001409" + ], + "decrease liver function": [ + "HP:0001410" + ], + "decreased liver function": [ + "HP:0001410" + ], + "hepatopathy": [ + "HP:0001410" + ], + "liver dysfunction": [ + "HP:0001410" + ], + "liver dysfunction , mild": [ + "HP:0001410" + ], + "enteroviral hepatitis": [ + "HP:0001412" + ], + "micronodular cirrhosis": [ + "HP:0001413" + ], + "microvesicular hepatic steatosis": [ + "HP:0001414" + ], + "microvesicular steatosis": [ + "HP:0001414" + ], + "x - link inheritance": [ + "HP:0001417" + ], + "x - linked inheritance": [ + "HP:0001417" + ], + "x - link": [ + "HP:0001417" + ], + "x - linked": [ + "HP:0001417" + ], + "x - link form": [ + "HP:0001417" + ], + "x - linked form": [ + "HP:0001417" + ], + "x - link recessive inheritance": [ + "HP:0001419" + ], + "x - linked recessive inheritance": [ + "HP:0001419" + ], + "x - link recessive": [ + "HP:0001419" + ], + "x - linked recessive": [ + "HP:0001419" + ], + "abnormality of the musculature of the hand": [ + "HP:0001421" + ], + "abnormal hand muscle": [ + "HP:0001421" + ], + "abnormal hand muscles": [ + "HP:0001421" + ], + "x - link dominant inheritance": [ + "HP:0001423" + ], + "x - linked dominant inheritance": [ + "HP:0001423" + ], + "x - link dominant": [ + "HP:0001423" + ], + "x - linked dominant": [ + "HP:0001423" + ], + "heterogeneous": [ + "HP:0001425" + ], + "genetic heterogeneity": [ + "HP:0001425" + ], + "heterogeneity": [ + "HP:0001425" + ], + "multifactorial inheritance": [ + "HP:0001426" + ], + "familial predisposition": [ + "HP:0001426" + ], + "mitochondrial inheritance": [ + "HP:0001427" + ], + "mitochondrial": [ + "HP:0001427" + ], + "somatic mutation": [ + "HP:0001428" + ], + "abnormality of the calf musculature": [ + "HP:0001430" + ], + "abnormal calf muscle": [ + "HP:0001430" + ], + "abnormal calf muscles": [ + "HP:0001430" + ], + "abnormality of calf musculature": [ + "HP:0001430" + ], + "hepatosplenomegaly": [ + "HP:0001433" + ], + "enlarge liver and spleen": [ + "HP:0001433" + ], + "enlarged liver and spleen": [ + "HP:0001433" + ], + "abnormality of the shoulder girdle musculature": [ + "HP:0001435" + ], + "abnormality of shoulder musculature": [ + "HP:0001435" + ], + "abnormality of the foot musculature": [ + "HP:0001436" + ], + "abnormal foot muscle": [ + "HP:0001436" + ], + "abnormal foot muscles": [ + "HP:0001436" + ], + "abnormality of the musculature of the low limb": [ + "HP:0001437" + ], + "abnormality of the musculature of the lower limbs": [ + "HP:0001437" + ], + "abnormal abdomen morphology": [ + "HP:0001438" + ], + "abdomen abnormality": [ + "HP:0001438" + ], + "abnormality of abdomen morphology": [ + "HP:0001438" + ], + "abnormality of abdomen structure": [ + "HP:0001438" + ], + "abnormality of the abdomen": [ + "HP:0001438" + ], + "metatarsal synostosis": [ + "HP:0001440" + ], + "fusion of metatarsal": [ + "HP:0001440" + ], + "fusion of metatarsals": [ + "HP:0001440" + ], + "fusion of the long bone of the foot": [ + "HP:0001440" + ], + "fusion of the long bones of the feet": [ + "HP:0001440" + ], + "synostosis involve metatarsal bone": [ + "HP:0001440" + ], + "synostosis involving metatarsal bones": [ + "HP:0001440" + ], + "abnormality of the musculature of the thigh": [ + "HP:0001441" + ], + "abnormal thigh muscle": [ + "HP:0001441" + ], + "abnormal thigh muscles": [ + "HP:0001441" + ], + "somatic mosaicism": [ + "HP:0001442" + ], + "abnormality of the gluteal musculature": [ + "HP:0001443" + ], + "abnormality of glute": [ + "HP:0001443" + ], + "abnormality of glutes": [ + "HP:0001443" + ], + "autosomal dominant somatic cell mutation": [ + "HP:0001444" + ], + "abnormality of the hip - girdle musculature": [ + "HP:0001445" + ], + "abnormality of the musculature of the upper limb": [ + "HP:0001446" + ], + "abnormality of the musculature of the upper limbs": [ + "HP:0001446" + ], + "abnormal upper limb muscle": [ + "HP:0001446" + ], + "abnormal upper limb muscles": [ + "HP:0001446" + ], + "duplication of metatarsal bone": [ + "HP:0001449" + ], + "duplication of metatarsal bones": [ + "HP:0001449" + ], + "duplication of long bone of foot": [ + "HP:0001449" + ], + "duplication of long bones of foot": [ + "HP:0001449" + ], + "y - link inheritance": [ + "HP:0001450" + ], + "y - linked inheritance": [ + "HP:0001450" + ], + "y - link": [ + "HP:0001450" + ], + "y - linked": [ + "HP:0001450" + ], + "autosomal dominant contiguous gene syndrome": [ + "HP:0001452" + ], + "abnormality of the upper arm": [ + "HP:0001454" + ], + "abnormality of the musculature of the upper arm": [ + "HP:0001457" + ], + "1 - 3 toe syndactyly": [ + "HP:0001459" + ], + "web 1st - 3rd toe": [ + "HP:0001459" + ], + "webbed 1st - 3rd toes": [ + "HP:0001459" + ], + "aplasia / hypoplasia involve the skeletal musculature": [ + "HP:0001460" + ], + "aplasia / hypoplasia involving the skeletal musculature": [ + "HP:0001460" + ], + "absent / small skeletal muscle": [ + "HP:0001460" + ], + "absent / small skeletal muscles": [ + "HP:0001460" + ], + "absent / underdevelop skeletal muscle": [ + "HP:0001460" + ], + "absent / underdeveloped skeletal muscles": [ + "HP:0001460" + ], + "aplasia / hypoplasia involve the shoulder musculature": [ + "HP:0001464" + ], + "aplasia / hypoplasia involving the shoulder musculature": [ + "HP:0001464" + ], + "absent / small shoulder muscle": [ + "HP:0001464" + ], + "absent / small shoulder muscles": [ + "HP:0001464" + ], + "absent / underdevelop shoulder muscle": [ + "HP:0001464" + ], + "absent / underdeveloped shoulder muscles": [ + "HP:0001464" + ], + "amyotrophy involve the shoulder musculature": [ + "HP:0001465" + ], + "amyotrophy involving the shoulder musculature": [ + "HP:0001465" + ], + "shoulder muscle degeneration": [ + "HP:0001465" + ], + "wasting of shoulder muscle": [ + "HP:0001465" + ], + "wasting of shoulder muscles": [ + "HP:0001465" + ], + "contiguous gene syndrome": [ + "HP:0001466" + ], + "aplasia / hypoplasia involve the musculature of the upper limb": [ + "HP:0001467" + ], + "aplasia / hypoplasia involving the musculature of the upper limbs": [ + "HP:0001467" + ], + "absent / small upper limb muscle": [ + "HP:0001467" + ], + "absent / small upper limb muscles": [ + "HP:0001467" + ], + "absent / underdevelop upper limb muscle": [ + "HP:0001467" + ], + "absent / underdeveloped upper limb muscles": [ + "HP:0001467" + ], + "aplasia / hypoplasia involve the musculature of the upper arm": [ + "HP:0001468" + ], + "aplasia / hypoplasia involving the musculature of the upper arm": [ + "HP:0001468" + ], + "absent / small upper arm muscle": [ + "HP:0001468" + ], + "absent / small upper arm muscles": [ + "HP:0001468" + ], + "absent / underdevelop upper arm muscle": [ + "HP:0001468" + ], + "absent / underdeveloped upper arm muscles": [ + "HP:0001468" + ], + "abnormal morphology of the pelvis musculature": [ + "HP:0001469" + ], + "abnormality of the musculature of the pelvis": [ + "HP:0001469" + ], + "sex - limited autosomal dominant": [ + "HP:0001470" + ], + "aplasia / hypoplasia of the musculature of the pelvis": [ + "HP:0001471" + ], + "absent / small pelvis muscle": [ + "HP:0001471" + ], + "absent / small pelvis muscles": [ + "HP:0001471" + ], + "absent / underdevelop pelvis muscle": [ + "HP:0001471" + ], + "absent / underdeveloped pelvis muscles": [ + "HP:0001471" + ], + "obsolete familial predisposition": [ + "HP:0001472" + ], + "metatarsal osteolysis": [ + "HP:0001473" + ], + "osteolysis involve metatarsal bone": [ + "HP:0001473" + ], + "osteolysis involving metatarsal bones": [ + "HP:0001473" + ], + "sclerotic scapula": [ + "HP:0001474" + ], + "sclerotic scapulae": [ + "HP:0001474" + ], + "male - limited autosomal dominant": [ + "HP:0001475" + ], + "delayed closure of the anterior fontanelle": [ + "HP:0001476" + ], + "delay closure anterior fontanel": [ + "HP:0001476" + ], + "delayed closure anterior fontanel": [ + "HP:0001476" + ], + "delayed closure of anterior fontanelle": [ + "HP:0001476" + ], + "delayed closure of the bregma suture": [ + "HP:0001476" + ], + "delayed closure of the bregma sutures": [ + "HP:0001476" + ], + "delayed closure of the soft spot on the skull": [ + "HP:0001476" + ], + "late closure of anterior fontanelle": [ + "HP:0001476" + ], + "late closure of large anterior fontanel": [ + "HP:0001476" + ], + "late closure of soft spot on the skull": [ + "HP:0001476" + ], + "late closure of the bregma suture": [ + "HP:0001476" + ], + "late closure of the bregma sutures": [ + "HP:0001476" + ], + "later than typical closing of soft spot of skull": [ + "HP:0001476" + ], + "persistent anterior fontanelle": [ + "HP:0001476" + ], + "compensatory chin elevation": [ + "HP:0001477" + ], + "compensatory head tilt / chin elevation": [ + "HP:0001477" + ], + "freckle": [ + "HP:0001480" + ], + "freckling": [ + "HP:0001480" + ], + "subcutaneous nodule": [ + "HP:0001482" + ], + "firm lump under the skin": [ + "HP:0001482" + ], + "growth of abnormal tissue under the skin": [ + "HP:0001482" + ], + "multiple , subcutaneous nodule": [ + "HP:0001482" + ], + "multiple , subcutaneous nodules": [ + "HP:0001482" + ], + "nodule below the skin": [ + "HP:0001482" + ], + "subcutaneous nodules": [ + "HP:0001482" + ], + "eye poking": [ + "HP:0001483" + ], + "obsolete hypopigmented fundus": [ + "HP:0001487" + ], + "obsolete hypopigmented fundi": [ + "HP:0001487" + ], + "bilateral ptosis": [ + "HP:0001488" + ], + "drooping of both upper eyelid": [ + "HP:0001488" + ], + "drooping of both upper eyelids": [ + "HP:0001488" + ], + "posterior vitreous detachment": [ + "HP:0001489" + ], + "vitreous detachment": [ + "HP:0001489" + ], + "congenital fibrosis of extraocular muscle": [ + "HP:0001491" + ], + "congenital fibrosis of extraocular muscles": [ + "HP:0001491" + ], + "congenital fibrosis of the extraocular muscle": [ + "HP:0001491" + ], + "congenital fibrosis of the extraocular muscles": [ + "HP:0001491" + ], + "congenital ophthalmoplegia": [ + "HP:0001491" + ], + "axenfeld anomaly": [ + "HP:0001492" + ], + "falciform retinal fold": [ + "HP:0001493" + ], + "congenital retinal fold": [ + "HP:0001493" + ], + "carpal osteolysis": [ + "HP:0001495" + ], + "carpal bone osteolysis": [ + "HP:0001495" + ], + "carpal bone hypoplasia": [ + "HP:0001498" + ], + "hypoplasia of carpal bone": [ + "HP:0001498" + ], + "hypoplasia of carpal bones": [ + "HP:0001498" + ], + "hypoplastic carpal bone": [ + "HP:0001498" + ], + "hypoplastic carpal bones": [ + "HP:0001498" + ], + "small carpal bone": [ + "HP:0001498" + ], + "small carpal bones": [ + "HP:0001498" + ], + "small carpal": [ + "HP:0001498" + ], + "small carpals": [ + "HP:0001498" + ], + "small wrist bone": [ + "HP:0001498" + ], + "small wrist bones": [ + "HP:0001498" + ], + "broad finger": [ + "HP:0001500" + ], + "broad fingers": [ + "HP:0001500" + ], + "wide finger": [ + "HP:0001500" + ], + "wide fingers": [ + "HP:0001500" + ], + "6 metacarpal": [ + "HP:0001501" + ], + "6 metacarpals": [ + "HP:0001501" + ], + "6 long bone of hand": [ + "HP:0001501" + ], + "6 long bones of hand": [ + "HP:0001501" + ], + "metacarpal osteolysis": [ + "HP:0001504" + ], + "metacarpals osteolysis": [ + "HP:0001504" + ], + "growth abnormality": [ + "HP:0001507" + ], + "abnormal growth": [ + "HP:0001507" + ], + "growth issue": [ + "HP:0001507" + ], + "failure to thrive": [ + "HP:0001508" + ], + "falter weight": [ + "HP:0001508" + ], + "faltering weight": [ + "HP:0001508" + ], + "poor weight gain": [ + "HP:0001508" + ], + "postnatal failure to thrive": [ + "HP:0001508" + ], + "undergrowth": [ + "HP:0001508" + ], + "weight falter": [ + "HP:0001508" + ], + "weight faltering": [ + "HP:0001508" + ], + "growth delay": [ + "HP:0001510" + ], + "delay growth": [ + "HP:0001510" + ], + "delayed growth": [ + "HP:0001510" + ], + "growth deficiency": [ + "HP:0001510" + ], + "growth failure": [ + "HP:0001510" + ], + "growth retardation": [ + "HP:0001510" + ], + "poor growth": [ + "HP:0001510" + ], + "retarded growth": [ + "HP:0001510" + ], + "very poor growth": [ + "HP:0001510" + ], + "intrauterine growth retardation": [ + "HP:0001511" + ], + "in utero growth retardation": [ + "HP:0001511" + ], + "intrauterine growth failure": [ + "HP:0001511" + ], + "intrauterine growth restriction": [ + "HP:0001511" + ], + "intrauterine growth retardation , iugr": [ + "HP:0001511" + ], + "intrauterine retardation": [ + "HP:0001511" + ], + "prenatal growth deficiency": [ + "HP:0001511" + ], + "prenatal growth failure": [ + "HP:0001511" + ], + "prenatal growth retardation": [ + "HP:0001511" + ], + "prenatal onset growth retardation": [ + "HP:0001511" + ], + "prenatal - onset growth retardation": [ + "HP:0001511" + ], + "small for gestational age infant": [ + "HP:0001511" + ], + "obesity": [ + "HP:0001513" + ], + "have too much body fat": [ + "HP:0001513" + ], + "having too much body fat": [ + "HP:0001513" + ], + "small for gestational age": [ + "HP:0001518" + ], + "birth weight less than 10th percentile": [ + "HP:0001518" + ], + "low birth weight": [ + "HP:0001518" + ], + "disproportionate tall stature": [ + "HP:0001519" + ], + "dolichostenomelia": [ + "HP:0001519" + ], + "marfanoid body habitus": [ + "HP:0001519" + ], + "marfanoid habitus": [ + "HP:0001519" + ], + "reduce upper - low segment ratio": [ + "HP:0001519" + ], + "reduced upper - lower segment ratio": [ + "HP:0001519" + ], + "large for gestational age": [ + "HP:0001520" + ], + "birth weight > 90th percentile": [ + "HP:0001520" + ], + "birthweight > 90th percentile": [ + "HP:0001520" + ], + "fetal macrosomia": [ + "HP:0001520" + ], + "foetal macrosomia": [ + "HP:0001520" + ], + "macrosomia": [ + "HP:0001520" + ], + "macrosomia , neonatal": [ + "HP:0001520" + ], + "death in infancy": [ + "HP:0001522" + ], + "death in early childhood": [ + "HP:0001522" + ], + "infantile death": [ + "HP:0001522" + ], + "lethal in infancy": [ + "HP:0001522" + ], + "severe failure to thrive": [ + "HP:0001525" + ], + "marked failure to thrive": [ + "HP:0001525" + ], + "severe falter weight": [ + "HP:0001525" + ], + "severe faltering weight": [ + "HP:0001525" + ], + "severe postnatal failure to thrive": [ + "HP:0001525" + ], + "severe weight faltering": [ + "HP:0001525" + ], + "hemihypertrophy": [ + "HP:0001528" + ], + "asymmetric limb hypertrophy": [ + "HP:0001528" + ], + "asymmetric overgrowth": [ + "HP:0001528" + ], + "mild postnatal growth retardation": [ + "HP:0001530" + ], + "mild growth deficiency": [ + "HP:0001530" + ], + "postnatal onset of mild growth retardation": [ + "HP:0001530" + ], + "failure to thrive in infancy": [ + "HP:0001531" + ], + "failure to thrive in first year of life": [ + "HP:0001531" + ], + "falter weight in infancy": [ + "HP:0001531" + ], + "faltering weight in infancy": [ + "HP:0001531" + ], + "weight falter in infancy": [ + "HP:0001531" + ], + "weight faltering in infancy": [ + "HP:0001531" + ], + "slender build": [ + "HP:0001533" + ], + "asthenic habitus": [ + "HP:0001533" + ], + "thin body habitus": [ + "HP:0001533" + ], + "thin build": [ + "HP:0001533" + ], + "umbilical hernia": [ + "HP:0001537" + ], + "umbilical hernias": [ + "HP:0001537" + ], + "protuberant abdomen": [ + "HP:0001538" + ], + "abdominal protuberance": [ + "HP:0001538" + ], + "belly stick out": [ + "HP:0001538" + ], + "belly sticks out": [ + "HP:0001538" + ], + "extend belly": [ + "HP:0001538" + ], + "extended belly": [ + "HP:0001538" + ], + "omphalocele": [ + "HP:0001539" + ], + "omphalocoele": [ + "HP:0001539" + ], + "diastasis rectus": [ + "HP:0001540" + ], + "diastasis recti": [ + "HP:0001540" + ], + "gap between large left and right abdominal muscle": [ + "HP:0001540" + ], + "gap between large left and right abdominal muscles": [ + "HP:0001540" + ], + "ascites": [ + "HP:0001541" + ], + "accumulation of fluid in the abdomen": [ + "HP:0001541" + ], + "gastroschisis": [ + "HP:0001543" + ], + "prominent umbilicus": [ + "HP:0001544" + ], + "prominent belly button": [ + "HP:0001544" + ], + "prominent navel": [ + "HP:0001544" + ], + "anteriorly place anus": [ + "HP:0001545" + ], + "anteriorly placed anus": [ + "HP:0001545" + ], + "anteriorly displace anus": [ + "HP:0001545" + ], + "anteriorly displaced anus": [ + "HP:0001545" + ], + "anus anteposition": [ + "HP:0001545" + ], + "abnormal rib cage morphology": [ + "HP:0001547" + ], + "abnormality of the rib cage": [ + "HP:0001547" + ], + "overgrowth": [ + "HP:0001548" + ], + "general overgrowth": [ + "HP:0001548" + ], + "generalise overgrowth": [ + "HP:0001548" + ], + "generalised overgrowth": [ + "HP:0001548" + ], + "generalize overgrowth": [ + "HP:0001548" + ], + "generalized overgrowth": [ + "HP:0001548" + ], + "abnormal ileum morphology": [ + "HP:0001549" + ], + "abnormality of the ileum": [ + "HP:0001549" + ], + "abnormal umbilicus morphology": [ + "HP:0001551" + ], + "abnormal belly button": [ + "HP:0001551" + ], + "abnormal navel": [ + "HP:0001551" + ], + "abnormal umbilicus": [ + "HP:0001551" + ], + "barrel - shape chest": [ + "HP:0001552" + ], + "barrel - shaped chest": [ + "HP:0001552" + ], + "barrel chest": [ + "HP:0001552" + ], + "asymmetry of the thorax": [ + "HP:0001555" + ], + "asymmetric chest": [ + "HP:0001555" + ], + "prenatal movement abnormality": [ + "HP:0001557" + ], + "abnormal intrauterine movement": [ + "HP:0001557" + ], + "abnormal intrauterine movements": [ + "HP:0001557" + ], + "decrease fetal movement": [ + "HP:0001558" + ], + "decreased fetal movement": [ + "HP:0001558" + ], + "decreased fetal activity": [ + "HP:0001558" + ], + "decreased fetal movements": [ + "HP:0001558" + ], + "decreased foetal activity": [ + "HP:0001558" + ], + "decrease foetal movement": [ + "HP:0001558" + ], + "decreased foetal movement": [ + "HP:0001558" + ], + "decreased foetal movements": [ + "HP:0001558" + ], + "decrease movement in utero": [ + "HP:0001558" + ], + "decreased movement in utero": [ + "HP:0001558" + ], + "fetal hypokinesia": [ + "HP:0001558" + ], + "foetal hypokinesia": [ + "HP:0001558" + ], + "less than 10 fetal movement in 12 hour": [ + "HP:0001558" + ], + "less than 10 fetal movements in 12 hours": [ + "HP:0001558" + ], + "less than 10 foetal movement in 12 hour": [ + "HP:0001558" + ], + "less than 10 foetal movements in 12 hours": [ + "HP:0001558" + ], + "reduce fetal movement": [ + "HP:0001558" + ], + "reduced fetal movement": [ + "HP:0001558" + ], + "reduced fetal movements": [ + "HP:0001558" + ], + "reduce foetal movement": [ + "HP:0001558" + ], + "reduced foetal movement": [ + "HP:0001558" + ], + "reduced foetal movements": [ + "HP:0001558" + ], + "abnormality of the amniotic fluid": [ + "HP:0001560" + ], + "abnormal amniotic fluid": [ + "HP:0001560" + ], + "polyhydramnios": [ + "HP:0001561" + ], + "high level of amniotic fluid": [ + "HP:0001561" + ], + "high levels of amniotic fluid": [ + "HP:0001561" + ], + "hydramnios": [ + "HP:0001561" + ], + "oligohydramnios": [ + "HP:0001562" + ], + "low level of amniotic fluid": [ + "HP:0001562" + ], + "low levels of amniotic fluid": [ + "HP:0001562" + ], + "maternal oligohydramnios": [ + "HP:0001562" + ], + "fetal polyuria": [ + "HP:0001563" + ], + "foetal polyuria": [ + "HP:0001563" + ], + "widely - space maxillary central incisor": [ + "HP:0001566" + ], + "widely - spaced maxillary central incisors": [ + "HP:0001566" + ], + "central incisor gap": [ + "HP:0001566" + ], + "diastasis of the central incisor": [ + "HP:0001566" + ], + "diastasis of the central incisors": [ + "HP:0001566" + ], + "diastema between maxillary central incisor": [ + "HP:0001566" + ], + "diastema between maxillary central incisors": [ + "HP:0001566" + ], + "diastema between upper front teeth": [ + "HP:0001566" + ], + "diastema between upper incisor": [ + "HP:0001566" + ], + "diastema between upper incisors": [ + "HP:0001566" + ], + "gap between upper front teeth": [ + "HP:0001566" + ], + "separate superior central incisor": [ + "HP:0001566" + ], + "separated superior central incisors": [ + "HP:0001566" + ], + "wide gap between upper central incisor": [ + "HP:0001566" + ], + "wide gap between upper central incisors": [ + "HP:0001566" + ], + "wide upper central incisor": [ + "HP:0001566" + ], + "wide upper central incisors": [ + "HP:0001566" + ], + "widely space upper incisor": [ + "HP:0001566" + ], + "widely spaced upper incisors": [ + "HP:0001566" + ], + "multiple impacted teeth": [ + "HP:0001571" + ], + "impact teeth": [ + "HP:0001571" + ], + "impacted teeth": [ + "HP:0001571" + ], + "multiple bury teeth": [ + "HP:0001571" + ], + "multiple buried teeth": [ + "HP:0001571" + ], + "multiple retain teeth": [ + "HP:0001571" + ], + "multiple retained teeth": [ + "HP:0001571" + ], + "macrodontia": [ + "HP:0001572" + ], + "hyperplasia of tooth": [ + "HP:0001572" + ], + "hypertrophy of tooth": [ + "HP:0001572" + ], + "increase size of tooth": [ + "HP:0001572" + ], + "increased size of tooth": [ + "HP:0001572" + ], + "increase width of tooth": [ + "HP:0001572" + ], + "increased width of tooth": [ + "HP:0001572" + ], + "large tooth": [ + "HP:0001572" + ], + "megalodontia": [ + "HP:0001572" + ], + "tooth mass excess": [ + "HP:0001572" + ], + "abnormality of the integument": [ + "HP:0001574" + ], + "obsolete mood change": [ + "HP:0001575" + ], + "obsolete mood changes": [ + "HP:0001575" + ], + "primary hypercortisolism": [ + "HP:0001579" + ], + "acth - independent hypercortisolemia": [ + "HP:0001579" + ], + "pigment micronodular adrenocortical disease": [ + "HP:0001580" + ], + "pigmented micronodular adrenocortical disease": [ + "HP:0001580" + ], + "recurrent skin infection": [ + "HP:0001581" + ], + "recurrent skin infections": [ + "HP:0001581" + ], + "cutaneous infection": [ + "HP:0001581" + ], + "cutaneous infections": [ + "HP:0001581" + ], + "skin infection , recurrent": [ + "HP:0001581" + ], + "skin infections , recurrent": [ + "HP:0001581" + ], + "redundant skin": [ + "HP:0001582" + ], + "loose redundant skin": [ + "HP:0001582" + ], + "redundant skin fold": [ + "HP:0001582" + ], + "redundant skin folds": [ + "HP:0001582" + ], + "sagging , redundant skin": [ + "HP:0001582" + ], + "rotary nystagmus": [ + "HP:0001583" + ], + "rotatory nystagmus": [ + "HP:0001583" + ], + "vesicovaginal fistula": [ + "HP:0001586" + ], + "obsolete primary ovarian failure": [ + "HP:0001587" + ], + "bell - shape thorax": [ + "HP:0001591" + ], + "bell - shaped thorax": [ + "HP:0001591" + ], + "bell - shape chest": [ + "HP:0001591" + ], + "bell - shaped chest": [ + "HP:0001591" + ], + "constrict , bell - shape thorax": [ + "HP:0001591" + ], + "constricted , bell - shaped thorax": [ + "HP:0001591" + ], + "narrow , bell - shape thorax": [ + "HP:0001591" + ], + "narrow , bell - shaped thorax": [ + "HP:0001591" + ], + "selective tooth agenesis": [ + "HP:0001592" + ], + "absence of a tooth": [ + "HP:0001592" + ], + "agenesis of a tooth": [ + "HP:0001592" + ], + "failure of development of a tooth": [ + "HP:0001592" + ], + "miss a tooth": [ + "HP:0001592" + ], + "missing a tooth": [ + "HP:0001592" + ], + "maxillary lateral incisor microdontia": [ + "HP:0001593" + ], + "decreased size of maxillary lateral incisor": [ + "HP:0001593" + ], + "decreased size of upper lateral incisor": [ + "HP:0001593" + ], + "decrease width of upper lateral incisor": [ + "HP:0001593" + ], + "decreased width of upper lateral incisor": [ + "HP:0001593" + ], + "hypotrophic maxillary lateral incisor": [ + "HP:0001593" + ], + "hypotrophic upper lateral incisor": [ + "HP:0001593" + ], + "small maxillary lateral incisor": [ + "HP:0001593" + ], + "small upper lateral incisor": [ + "HP:0001593" + ], + "abnormal hair morphology": [ + "HP:0001595" + ], + "abnormality of the hair": [ + "HP:0001595" + ], + "abnormality of the hair shaft": [ + "HP:0001595" + ], + "hair abnormality": [ + "HP:0001595" + ], + "alopecia": [ + "HP:0001596" + ], + "hair loss": [ + "HP:0001596" + ], + "abnormality of the nail": [ + "HP:0001597" + ], + "nail disease": [ + "HP:0001597" + ], + "concave nail": [ + "HP:0001598" + ], + "koilonychia": [ + "HP:0001598" + ], + "spoon - shape nail": [ + "HP:0001598" + ], + "spoon - shaped nails": [ + "HP:0001598" + ], + "abnormality of the larynx": [ + "HP:0001600" + ], + "laryngeal abnormality": [ + "HP:0001600" + ], + "laryngeal abnormalities": [ + "HP:0001600" + ], + "laryngeal anomaly": [ + "HP:0001600" + ], + "laryngeal anomalies": [ + "HP:0001600" + ], + "laryngomalacia": [ + "HP:0001601" + ], + "softening of voice box tissue": [ + "HP:0001601" + ], + "laryngeal stenosis": [ + "HP:0001602" + ], + "vocal cord paresis": [ + "HP:0001604" + ], + "hoarse voice due to vocal cord paresis": [ + "HP:0001604" + ], + "vocal cord paresis in severe case": [ + "HP:0001604" + ], + "vocal cord paresis in severe cases": [ + "HP:0001604" + ], + "weakness of the vocal cord": [ + "HP:0001604" + ], + "weakness of the vocal cords": [ + "HP:0001604" + ], + "vocal cord paralysis": [ + "HP:0001605" + ], + "inability to move vocal cord": [ + "HP:0001605" + ], + "inability to move vocal cords": [ + "HP:0001605" + ], + "laryngeal paralysis": [ + "HP:0001605" + ], + "obsolete vocal cord paralysis ( cause by tumor impingement )": [ + "HP:0001606" + ], + "obsolete vocal cord paralysis ( caused by tumor impingement )": [ + "HP:0001606" + ], + "subglottic stenosis": [ + "HP:0001607" + ], + "abnormality of the voice": [ + "HP:0001608" + ], + "voice abnormality": [ + "HP:0001608" + ], + "hoarse voice": [ + "HP:0001609" + ], + "hoarseness": [ + "HP:0001609" + ], + "husky voice": [ + "HP:0001609" + ], + "nasal speech": [ + "HP:0001611" + ], + "hypernasal speech": [ + "HP:0001611" + ], + "hypernasal voice": [ + "HP:0001611" + ], + "nasal voice": [ + "HP:0001611" + ], + "weak cry": [ + "HP:0001612" + ], + "obsolete hoarse voice ( cause by tumor impingement )": [ + "HP:0001613" + ], + "obsolete hoarse voice ( caused by tumor impingement )": [ + "HP:0001613" + ], + "hoarse cry": [ + "HP:0001615" + ], + "dysphonia": [ + "HP:0001618" + ], + "inability to produce voice sound": [ + "HP:0001618" + ], + "inability to produce voice sounds": [ + "HP:0001618" + ], + "voice change": [ + "HP:0001618" + ], + "high pitch voice": [ + "HP:0001620" + ], + "high pitched voice": [ + "HP:0001620" + ], + "high - pitched voice": [ + "HP:0001620" + ], + "weak voice": [ + "HP:0001621" + ], + "hypophonia": [ + "HP:0001621" + ], + "soft voice": [ + "HP:0001621" + ], + "premature birth": [ + "HP:0001622" + ], + "premature delivery": [ + "HP:0001622" + ], + "premature delivery of affected infant": [ + "HP:0001622" + ], + "premature delivery of affected infants": [ + "HP:0001622" + ], + "preterm delivery": [ + "HP:0001622" + ], + "shorten gestation time": [ + "HP:0001622" + ], + "shortened gestation time": [ + "HP:0001622" + ], + "breech presentation": [ + "HP:0001623" + ], + "breech presentation at birth": [ + "HP:0001623" + ], + "foot or buttock of fetus position near opening of uterus": [ + "HP:0001623" + ], + "feet or buttocks of fetus positioned near opening of uterus": [ + "HP:0001623" + ], + "foot or buttock of foetus position near opening of uterus": [ + "HP:0001623" + ], + "feet or buttocks of foetus positioned near opening of uterus": [ + "HP:0001623" + ], + "abnormality of the cardiovascular system": [ + "HP:0001626" + ], + "cardiovascular abnormality": [ + "HP:0001626" + ], + "cardiovascular disease": [ + "HP:0001626" + ], + "abnormal heart morphology": [ + "HP:0001627" + ], + "abnormality of cardiac morphology": [ + "HP:0001627" + ], + "abnormality of the heart": [ + "HP:0001627" + ], + "abnormally shaped heart": [ + "HP:0001627" + ], + "cardiac abnormality": [ + "HP:0001627" + ], + "cardiac anomaly": [ + "HP:0001627" + ], + "cardiac anomalies": [ + "HP:0001627" + ], + "congenital heart defect": [ + "HP:0001627" + ], + "congenital heart defects": [ + "HP:0001627" + ], + "heart defect": [ + "HP:0001627" + ], + "ventricular septal defect": [ + "HP:0001629" + ], + "hole in heart wall separate two low heart chamber": [ + "HP:0001629" + ], + "hole in heart wall separating two lower heart chambers": [ + "HP:0001629" + ], + "ventricular septal defects": [ + "HP:0001629" + ], + "ventriculoseptal defect": [ + "HP:0001629" + ], + "atrial septal defect": [ + "HP:0001631" + ], + "an opening in the wall separate the top two chamber of the heart": [ + "HP:0001631" + ], + "an opening in the wall separating the top two chambers of the heart": [ + "HP:0001631" + ], + "atrium septal defect": [ + "HP:0001631" + ], + "atria septal defect": [ + "HP:0001631" + ], + "atrial septum defect": [ + "HP:0001631" + ], + "atrioseptal defect": [ + "HP:0001631" + ], + "defect in the atrial septum": [ + "HP:0001631" + ], + "hole in heart wall separate two upper heart chamber": [ + "HP:0001631" + ], + "hole in heart wall separating two upper heart chambers": [ + "HP:0001631" + ], + "abnormal mitral valve morphology": [ + "HP:0001633" + ], + "abnormality of the mitral valve": [ + "HP:0001633" + ], + "mitral valve prolapse": [ + "HP:0001634" + ], + "congestive heart failure": [ + "HP:0001635" + ], + "cardiac failure": [ + "HP:0001635" + ], + "cardiac failures": [ + "HP:0001635" + ], + "cardiac insufficiency": [ + "HP:0001635" + ], + "chronic heart failure": [ + "HP:0001635" + ], + "heart failure": [ + "HP:0001635" + ], + "tetralogy of fallot": [ + "HP:0001636" + ], + "tetrology of fallot": [ + "HP:0001636" + ], + "abnormal myocardium morphology": [ + "HP:0001637" + ], + "abnormality of the myocardium": [ + "HP:0001637" + ], + "cardiomyopathy": [ + "HP:0001638" + ], + "disease of the heart muscle": [ + "HP:0001638" + ], + "hypertrophic cardiomyopathy": [ + "HP:0001639" + ], + "cardiomyopathy , hypertrophic": [ + "HP:0001639" + ], + "enlarge and thicken heart muscle": [ + "HP:0001639" + ], + "enlarged and thickened heart muscle": [ + "HP:0001639" + ], + "cardiomegaly": [ + "HP:0001640" + ], + "enlarge heart": [ + "HP:0001640" + ], + "enlarged heart": [ + "HP:0001640" + ], + "increase heart size": [ + "HP:0001640" + ], + "increased heart size": [ + "HP:0001640" + ], + "abnormal pulmonary valve morphology": [ + "HP:0001641" + ], + "abnormality of the pulmonary valve": [ + "HP:0001641" + ], + "anomaly of the pulmonary valve": [ + "HP:0001641" + ], + "pulmonic stenosis": [ + "HP:0001642" + ], + "narrowing of pulmonic valve": [ + "HP:0001642" + ], + "pulmonary stenosis": [ + "HP:0001642" + ], + "pulmonary valve stenosis": [ + "HP:0001642" + ], + "pulmonic valve stenosis": [ + "HP:0001642" + ], + "patent ductus arteriosus": [ + "HP:0001643" + ], + "ductus arteriosus": [ + "HP:0001643" + ], + "persistent arterial duct": [ + "HP:0001643" + ], + "persistent ductus arteriosus": [ + "HP:0001643" + ], + "dilate cardiomyopathy": [ + "HP:0001644" + ], + "dilated cardiomyopathy": [ + "HP:0001644" + ], + "cardiomyopathy , dilate": [ + "HP:0001644" + ], + "cardiomyopathy , dilated": [ + "HP:0001644" + ], + "congestive cardiomyopathy": [ + "HP:0001644" + ], + "stretch and thin heart muscle": [ + "HP:0001644" + ], + "stretched and thinned heart muscle": [ + "HP:0001644" + ], + "sudden cardiac death": [ + "HP:0001645" + ], + "premature sudden cardiac death": [ + "HP:0001645" + ], + "abnormal aortic valve morphology": [ + "HP:0001646" + ], + "abnormality of the aortic valve": [ + "HP:0001646" + ], + "bicuspid aortic valve": [ + "HP:0001647" + ], + "aortic valve have two leaflet rather than three": [ + "HP:0001647" + ], + "aortic valve has two leaflets rather than three": [ + "HP:0001647" + ], + "cor pulmonale": [ + "HP:0001648" + ], + "tachycardia": [ + "HP:0001649" + ], + "elevate heart rate": [ + "HP:0001649" + ], + "elevated heart rate": [ + "HP:0001649" + ], + "fast heart rate": [ + "HP:0001649" + ], + "heart race": [ + "HP:0001649" + ], + "heart racing": [ + "HP:0001649" + ], + "increase heart rate": [ + "HP:0001649" + ], + "increased heart rate": [ + "HP:0001649" + ], + "race heart": [ + "HP:0001649" + ], + "racing heart": [ + "HP:0001649" + ], + "rapid heart beat": [ + "HP:0001649" + ], + "aortic valve stenosis": [ + "HP:0001650" + ], + "aortic stenosis": [ + "HP:0001650" + ], + "narrowing of aortic valve": [ + "HP:0001650" + ], + "valvular aortic stenosis": [ + "HP:0001650" + ], + "dextrocardia": [ + "HP:0001651" + ], + "heart tip and four chamber point towards right side of body": [ + "HP:0001651" + ], + "heart tip and four chambers point towards right side of body": [ + "HP:0001651" + ], + "thoracic situs inversus": [ + "HP:0001651" + ], + "mitral regurgitation": [ + "HP:0001653" + ], + "mitral incompetence": [ + "HP:0001653" + ], + "mitral insufficiency": [ + "HP:0001653" + ], + "mitral regurgitation , mild": [ + "HP:0001653" + ], + "mitral valve insufficiency": [ + "HP:0001653" + ], + "mitral valve regurgitation": [ + "HP:0001653" + ], + "abnormal heart valve morphology": [ + "HP:0001654" + ], + "abnormality of the heart valve": [ + "HP:0001654" + ], + "abnormality of the heart valves": [ + "HP:0001654" + ], + "valvular abnormality": [ + "HP:0001654" + ], + "valvular heart disease": [ + "HP:0001654" + ], + "patent foramen ovale": [ + "HP:0001655" + ], + "persistent foramen ovale": [ + "HP:0001655" + ], + "prolonged qt interval": [ + "HP:0001657" + ], + "long q - t syndrome": [ + "HP:0001657" + ], + "long qt syndrome": [ + "HP:0001657" + ], + "prolong qt interval on ekg": [ + "HP:0001657" + ], + "myocardial infarction": [ + "HP:0001658" + ], + "heart attack": [ + "HP:0001658" + ], + "aortic regurgitation": [ + "HP:0001659" + ], + "aortic insufficiency": [ + "HP:0001659" + ], + "aortic valve regurgitation": [ + "HP:0001659" + ], + "truncus arteriosus": [ + "HP:0001660" + ], + "common arterial trunk": [ + "HP:0001660" + ], + "persistant truncus arteriosus": [ + "HP:0001660" + ], + "bradycardia": [ + "HP:0001662" + ], + "brachycardia": [ + "HP:0001662" + ], + "slow heartbeat": [ + "HP:0001662" + ], + "slow heartbeats": [ + "HP:0001662" + ], + "ventricular fibrillation": [ + "HP:0001663" + ], + "torsade de pointes": [ + "HP:0001664" + ], + "torsades de pointes": [ + "HP:0001664" + ], + "right ventricular hypertrophy": [ + "HP:0001667" + ], + "heart right ventricle hypertrophy": [ + "HP:0001667" + ], + "transposition of the great artery": [ + "HP:0001669" + ], + "transposition of the great arteries": [ + "HP:0001669" + ], + "transposition of great vessel": [ + "HP:0001669" + ], + "transposition of great vessels": [ + "HP:0001669" + ], + "asymmetric septal hypertrophy": [ + "HP:0001670" + ], + "abnormal cardiac septum morphology": [ + "HP:0001671" + ], + "abnormality of the cardiac septum": [ + "HP:0001671" + ], + "abnormality of the cardiac septa": [ + "HP:0001671" + ], + "heart septal defect": [ + "HP:0001671" + ], + "septal defect": [ + "HP:0001671" + ], + "septal defects": [ + "HP:0001671" + ], + "obsolete tachycardia ( with pheochromocytoma )": [ + "HP:0001673" + ], + "complete atrioventricular canal defect": [ + "HP:0001674" + ], + "atrioventricular canal": [ + "HP:0001674" + ], + "common atrioventricular canal": [ + "HP:0001674" + ], + "complete atrioventricular septal defect": [ + "HP:0001674" + ], + "complete common av canal": [ + "HP:0001674" + ], + "obsolete rhythm disturbance associate with pheochromocytoma": [ + "HP:0001675" + ], + "obsolete rhythm disturbances associated with pheochromocytoma": [ + "HP:0001675" + ], + "obsolete palpitation ( with pheochromocytoma )": [ + "HP:0001676" + ], + "obsolete palpitations ( with pheochromocytoma )": [ + "HP:0001676" + ], + "coronary artery atherosclerosis": [ + "HP:0001677" + ], + "coronary atherosclerosis": [ + "HP:0001677" + ], + "coronary disease": [ + "HP:0001677" + ], + "plaque build - up in artery supply blood to heart": [ + "HP:0001677" + ], + "plaque build - up in arteries supplying blood to heart": [ + "HP:0001677" + ], + "atrioventricular block": [ + "HP:0001678" + ], + "atrioventricular nodal disease": [ + "HP:0001678" + ], + "interruption of electrical communication between upper and low chamber of heart": [ + "HP:0001678" + ], + "interruption of electrical communication between upper and lower chambers of heart": [ + "HP:0001678" + ], + "abnormal aortic morphology": [ + "HP:0001679" + ], + "abnormal aorta morphology": [ + "HP:0001679" + ], + "abnormality of the aorta": [ + "HP:0001679" + ], + "coarctation of aorta": [ + "HP:0001680" + ], + "aortic coarctation": [ + "HP:0001680" + ], + "coarctation of the aorta": [ + "HP:0001680" + ], + "narrowing of aorta": [ + "HP:0001680" + ], + "narrowing of the aorta": [ + "HP:0001680" + ], + "angina pectoris": [ + "HP:0001681" + ], + "subvalvular aortic stenosis": [ + "HP:0001682" + ], + "narrowing of blood vessel below aortic heart valve": [ + "HP:0001682" + ], + "subaortic stenosis": [ + "HP:0001682" + ], + "ectopia cordis": [ + "HP:0001683" + ], + "secundum atrial septal defect": [ + "HP:0001684" + ], + "atrial septal defect , ostium secundum type": [ + "HP:0001684" + ], + "ostium secundum atrial septal defect": [ + "HP:0001684" + ], + "patent ostium secundum": [ + "HP:0001684" + ], + "myocardial fibrosis": [ + "HP:0001685" + ], + "loss of voice": [ + "HP:0001686" + ], + "aphonia": [ + "HP:0001686" + ], + "sinus bradycardia": [ + "HP:0001688" + ], + "muscular subvalvular aortic stenosis": [ + "HP:0001691" + ], + "muscular subaortic stenosis": [ + "HP:0001691" + ], + "atrial arrhythmia": [ + "HP:0001692" + ], + "primary atrial arrhythmia": [ + "HP:0001692" + ], + "cardiac shunt": [ + "HP:0001693" + ], + "right - to - left shunt": [ + "HP:0001694" + ], + "cardiac arrest": [ + "HP:0001695" + ], + "heart stop beat": [ + "HP:0001695" + ], + "heart stops beating": [ + "HP:0001695" + ], + "situs inversus totalis": [ + "HP:0001696" + ], + "all organ on wrong side of body": [ + "HP:0001696" + ], + "all organs on wrong side of body": [ + "HP:0001696" + ], + "situs inversus": [ + "HP:0001696" + ], + "situs oppositus": [ + "HP:0001696" + ], + "situs transversus": [ + "HP:0001696" + ], + "abnormal pericardium morphology": [ + "HP:0001697" + ], + "abnormality of the pericardium": [ + "HP:0001697" + ], + "pericardial effusion": [ + "HP:0001698" + ], + "fluid around heart": [ + "HP:0001698" + ], + "pericardial effusions": [ + "HP:0001698" + ], + "sudden death": [ + "HP:0001699" + ], + "myocardial necrosis": [ + "HP:0001700" + ], + "pericarditis": [ + "HP:0001701" + ], + "swell or irritation of membrane around heart": [ + "HP:0001701" + ], + "swelling or irritation of membrane around heart": [ + "HP:0001701" + ], + "abnormal tricuspid valve morphology": [ + "HP:0001702" + ], + "abnormality of the tricuspid valve": [ + "HP:0001702" + ], + "tricuspid valve prolapse": [ + "HP:0001704" + ], + "right ventricular outlet tract obstruction": [ + "HP:0001705" + ], + "right ventricular outlet obstruction": [ + "HP:0001705" + ], + "endocardial fibroelastosis": [ + "HP:0001706" + ], + "abnormal right ventricle morphology": [ + "HP:0001707" + ], + "abnormality of the right ventricle": [ + "HP:0001707" + ], + "right ventricular abnormality": [ + "HP:0001707" + ], + "right ventricular failure": [ + "HP:0001708" + ], + "impaired right ventricular function": [ + "HP:0001708" + ], + "right ventricular impairment": [ + "HP:0001708" + ], + "right - side heart failure": [ + "HP:0001708" + ], + "right - sided heart failure": [ + "HP:0001708" + ], + "third degree atrioventricular block": [ + "HP:0001709" + ], + "complete heart block": [ + "HP:0001709" + ], + "third - degree heart block": [ + "HP:0001709" + ], + "conotruncal defect": [ + "HP:0001710" + ], + "conotruncal heart defect": [ + "HP:0001710" + ], + "conotruncal heart defects": [ + "HP:0001710" + ], + "abnormal leave ventricle morphology": [ + "HP:0001711" + ], + "abnormal left ventricle morphology": [ + "HP:0001711" + ], + "abnormal heart leave ventricle morphology": [ + "HP:0001711" + ], + "abnormal heart left ventricle morphology": [ + "HP:0001711" + ], + "abnormality of the left ventricle": [ + "HP:0001711" + ], + "leave ventricular abnormality": [ + "HP:0001711" + ], + "left ventricular abnormality": [ + "HP:0001711" + ], + "leave ventricular hypertrophy": [ + "HP:0001712" + ], + "left ventricular hypertrophy": [ + "HP:0001712" + ], + "heart leave ventricle hypertrophy": [ + "HP:0001712" + ], + "heart left ventricle hypertrophy": [ + "HP:0001712" + ], + "leave ventricular wall hypertrophy": [ + "HP:0001712" + ], + "left ventricular wall hypertrophy": [ + "HP:0001712" + ], + "abnormal cardiac ventricle morphology": [ + "HP:0001713" + ], + "abnormality of cardiac ventricle": [ + "HP:0001713" + ], + "ventricular hypertrophy": [ + "HP:0001714" + ], + "wolff - parkinson - white syndrome": [ + "HP:0001716" + ], + "coronary artery calcification": [ + "HP:0001717" + ], + "mitral stenosis": [ + "HP:0001718" + ], + "mitral valve stenosis": [ + "HP:0001718" + ], + "double outlet right ventricle": [ + "HP:0001719" + ], + "double - outlet right ventricle": [ + "HP:0001719" + ], + "high - output congestive heart failure": [ + "HP:0001722" + ], + "restrictive cardiomyopathy": [ + "HP:0001723" + ], + "obsolete aortic dilatation": [ + "HP:0001724" + ], + "obsolete increase prevalence of valvular disease": [ + "HP:0001726" + ], + "obsolete increased prevalence of valvular disease": [ + "HP:0001726" + ], + "thromboembolic stroke": [ + "HP:0001727" + ], + "progressive hearing impairment": [ + "HP:0001730" + ], + "progressive hearing loss": [ + "HP:0001730" + ], + "abnormality of the pancreas": [ + "HP:0001732" + ], + "pancreatic disease": [ + "HP:0001732" + ], + "pancreatitis": [ + "HP:0001733" + ], + "pancreatic inflammation": [ + "HP:0001733" + ], + "annular pancreas": [ + "HP:0001734" + ], + "acute pancreatitis": [ + "HP:0001735" + ], + "acute pancreatic inflammation": [ + "HP:0001735" + ], + "pancreatitis , acute": [ + "HP:0001735" + ], + "pancreatic cyst": [ + "HP:0001737" + ], + "pancreatic cysts": [ + "HP:0001737" + ], + "multiple pancreatic cyst": [ + "HP:0001737" + ], + "multiple pancreatic cysts": [ + "HP:0001737" + ], + "exocrine pancreatic insufficiency": [ + "HP:0001738" + ], + "inability to properly digest food due to lack of pancreatic digestive enzyme": [ + "HP:0001738" + ], + "inability to properly digest food due to lack of pancreatic digestive enzymes": [ + "HP:0001738" + ], + "pancreatic insufficiency": [ + "HP:0001738" + ], + "abnormal nasopharynx morphology": [ + "HP:0001739" + ], + "abnormality of the nasopharynx": [ + "HP:0001739" + ], + "phimosis": [ + "HP:0001741" + ], + "nasal congestion": [ + "HP:0001742" + ], + "blockage of nose": [ + "HP:0001742" + ], + "congestion of nose": [ + "HP:0001742" + ], + "nasal blockage": [ + "HP:0001742" + ], + "nasal obstruction": [ + "HP:0001742" + ], + "obstruction of nose": [ + "HP:0001742" + ], + "stuffy nose": [ + "HP:0001742" + ], + "abnormality of the spleen": [ + "HP:0001743" + ], + "splenomegaly": [ + "HP:0001744" + ], + "increase spleen size": [ + "HP:0001744" + ], + "increased spleen size": [ + "HP:0001744" + ], + "asplenia": [ + "HP:0001746" + ], + "absent spleen": [ + "HP:0001746" + ], + "accessory spleen": [ + "HP:0001747" + ], + "polysplenia": [ + "HP:0001748" + ], + "accessory spleens": [ + "HP:0001748" + ], + "multiple accessory spleen": [ + "HP:0001748" + ], + "multiple accessory spleens": [ + "HP:0001748" + ], + "multiple small spleen": [ + "HP:0001748" + ], + "multiple small spleens": [ + "HP:0001748" + ], + "single ventricle": [ + "HP:0001750" + ], + "common ventricle": [ + "HP:0001750" + ], + "vestibular dysfunction": [ + "HP:0001751" + ], + "impaired vestibular function": [ + "HP:0001751" + ], + "interictal vestibular dysfunction": [ + "HP:0001751" + ], + "vestibular function defect": [ + "HP:0001751" + ], + "vestibular hypofunction": [ + "HP:0001756" + ], + "high - frequency sensorineural hearing impairment": [ + "HP:0001757" + ], + "high frequency sensorineural hearing impairment": [ + "HP:0001757" + ], + "high - tone sensorineural deafness": [ + "HP:0001757" + ], + "high - tone sensorineural hearing impairment": [ + "HP:0001757" + ], + "abnormal foot morphology": [ + "HP:0001760" + ], + "abnormal foot structure": [ + "HP:0001760" + ], + "abnormal feet structure": [ + "HP:0001760" + ], + "abnormality of the foot": [ + "HP:0001760" + ], + "abnormality of the feet": [ + "HP:0001760" + ], + "foot deformity": [ + "HP:0001760" + ], + "foot deformities": [ + "HP:0001760" + ], + "pe cavus": [ + "HP:0001761" + ], + "pes cavus": [ + "HP:0001761" + ], + "high - arched foot": [ + "HP:0001761" + ], + "talipes equinovarus": [ + "HP:0001762" + ], + "club foot": [ + "HP:0001762" + ], + "club feet": [ + "HP:0001762" + ], + "clubbing of foot": [ + "HP:0001762" + ], + "clubbing of feet": [ + "HP:0001762" + ], + "clubfeet": [ + "HP:0001762" + ], + "clubfoot": [ + "HP:0001762" + ], + "equinovarus": [ + "HP:0001762" + ], + "foot , talipes equinovarus": [ + "HP:0001762" + ], + "pe equinovarus": [ + "HP:0001762" + ], + "pes equinovarus": [ + "HP:0001762" + ], + "pe equinus": [ + "HP:0001762" + ], + "pes equinus": [ + "HP:0001762" + ], + "talipes varus": [ + "HP:0001762" + ], + "pe planus": [ + "HP:0001763" + ], + "pes planus": [ + "HP:0001763" + ], + "drop arch": [ + "HP:0001763" + ], + "dropped arches": [ + "HP:0001763" + ], + "fall arch": [ + "HP:0001763" + ], + "fallen arches": [ + "HP:0001763" + ], + "flat foot": [ + "HP:0001763" + ], + "flat feet": [ + "HP:0001763" + ], + "hammertoe": [ + "HP:0001765" + ], + "hammer toe": [ + "HP:0001765" + ], + "hammertoes": [ + "HP:0001765" + ], + "broad foot": [ + "HP:0001769" + ], + "broad feet": [ + "HP:0001769" + ], + "wide foot": [ + "HP:0001769" + ], + "toe syndactyly": [ + "HP:0001770" + ], + "foot syndactyly": [ + "HP:0001770" + ], + "fuse toe": [ + "HP:0001770" + ], + "fused toes": [ + "HP:0001770" + ], + "syndactyly of foot": [ + "HP:0001770" + ], + "syndactyly of feet": [ + "HP:0001770" + ], + "syndactyly of toe": [ + "HP:0001770" + ], + "syndactyly of toes": [ + "HP:0001770" + ], + "webbed toe": [ + "HP:0001770" + ], + "webbed toes": [ + "HP:0001770" + ], + "achilles tendon contracture": [ + "HP:0001771" + ], + "achilles tendon contractures": [ + "HP:0001771" + ], + "contracture of the achilles tendon": [ + "HP:0001771" + ], + "contractures of the achilles tendon": [ + "HP:0001771" + ], + "shortening of the achilles tendon": [ + "HP:0001771" + ], + "tight achilles tendon": [ + "HP:0001771" + ], + "talipes equinovalgus": [ + "HP:0001772" + ], + "equinovalgus deformity": [ + "HP:0001772" + ], + "short foot": [ + "HP:0001773" + ], + "hypoplastic foot": [ + "HP:0001773" + ], + "hypoplastic feet": [ + "HP:0001773" + ], + "short feet": [ + "HP:0001773" + ], + "small foot": [ + "HP:0001773" + ], + "small feet": [ + "HP:0001773" + ], + "tarsal osteovalgus": [ + "HP:0001775" + ], + "bilateral talipes equinovarus": [ + "HP:0001776" + ], + "bilateral clubfeet": [ + "HP:0001776" + ], + "bilateral clubfoot": [ + "HP:0001776" + ], + "club foot on both side": [ + "HP:0001776" + ], + "club foot on both sides": [ + "HP:0001776" + ], + "abnormality of toe": [ + "HP:0001780" + ], + "abnormality of the toe": [ + "HP:0001780" + ], + "abnormalities of the toes": [ + "HP:0001780" + ], + "bulbous tip of toe": [ + "HP:0001782" + ], + "bulbous tips of toes": [ + "HP:0001782" + ], + "broad metatarsal": [ + "HP:0001783" + ], + "broad metatarsals": [ + "HP:0001783" + ], + "wide long bone of foot": [ + "HP:0001783" + ], + "widen metatarsal shaft": [ + "HP:0001783" + ], + "widened metatarsal shaft": [ + "HP:0001783" + ], + "ankle swell": [ + "HP:0001785" + ], + "ankle swelling": [ + "HP:0001785" + ], + "narrow foot": [ + "HP:0001786" + ], + "slender foot": [ + "HP:0001786" + ], + "slender feet": [ + "HP:0001786" + ], + "abnormal delivery": [ + "HP:0001787" + ], + "delivery complication": [ + "HP:0001787" + ], + "premature rupture of membrane": [ + "HP:0001788" + ], + "premature rupture of membranes": [ + "HP:0001788" + ], + "hydrops fetalis": [ + "HP:0001789" + ], + "nonimmune hydrops fetalis": [ + "HP:0001790" + ], + "hydrops fetalis , non - immune": [ + "HP:0001790" + ], + "hydrops fetalis , nonimmune": [ + "HP:0001790" + ], + "non - immune fetal hydrops": [ + "HP:0001790" + ], + "non - immune foetal hydrops": [ + "HP:0001790" + ], + "nonimmune hydrops": [ + "HP:0001790" + ], + "fetal ascites": [ + "HP:0001791" + ], + "foetal ascites": [ + "HP:0001791" + ], + "small nail": [ + "HP:0001792" + ], + "hypoplastic nail": [ + "HP:0001792" + ], + "hypoplastic nails": [ + "HP:0001792" + ], + "nail hypoplasia": [ + "HP:0001792" + ], + "small nails": [ + "HP:0001792" + ], + "hyperconvex nail": [ + "HP:0001795" + ], + "increase nail curvature": [ + "HP:0001795" + ], + "increased nail curvature": [ + "HP:0001795" + ], + "nail overcurvature": [ + "HP:0001795" + ], + "anonychia": [ + "HP:0001798" + ], + "absent nail": [ + "HP:0001798" + ], + "absent nails": [ + "HP:0001798" + ], + "aplastic nail": [ + "HP:0001798" + ], + "aplastic nails": [ + "HP:0001798" + ], + "short nail": [ + "HP:0001799" + ], + "short nails": [ + "HP:0001799" + ], + "hypoplastic toenail": [ + "HP:0001800" + ], + "hypoplastic toenails": [ + "HP:0001800" + ], + "underdeveloped toenail": [ + "HP:0001800" + ], + "underdeveloped toenails": [ + "HP:0001800" + ], + "absent toenail": [ + "HP:0001802" + ], + "absent toenails": [ + "HP:0001802" + ], + "absent toenail ( anonychia )": [ + "HP:0001802" + ], + "absent toenails ( anonychia )": [ + "HP:0001802" + ], + "anonychia of toenail": [ + "HP:0001802" + ], + "anonychia of toenails": [ + "HP:0001802" + ], + "nail pit": [ + "HP:0001803" + ], + "nail pits": [ + "HP:0001803" + ], + "nail pitting": [ + "HP:0001803" + ], + "pit nail": [ + "HP:0001803" + ], + "pitted nails": [ + "HP:0001803" + ], + "hypoplastic fingernail": [ + "HP:0001804" + ], + "small fingernail": [ + "HP:0001804" + ], + "underdeveloped fingernail": [ + "HP:0001804" + ], + "onychogryposis": [ + "HP:0001805" + ], + "dystrophic thicken nail": [ + "HP:0001805" + ], + "dystrophic thickened nails": [ + "HP:0001805" + ], + "thick nail": [ + "HP:0001805" + ], + "thicken nail": [ + "HP:0001805" + ], + "thickened nails": [ + "HP:0001805" + ], + "onycholysis": [ + "HP:0001806" + ], + "detachment of nail": [ + "HP:0001806" + ], + "oncholysis": [ + "HP:0001806" + ], + "ridge nail": [ + "HP:0001807" + ], + "ridged nail": [ + "HP:0001807" + ], + "groove nail": [ + "HP:0001807" + ], + "grooved nails": [ + "HP:0001807" + ], + "longitudinal ridging": [ + "HP:0001807" + ], + "nail ridging": [ + "HP:0001807" + ], + "ridged nails": [ + "HP:0001807" + ], + "fragile nail": [ + "HP:0001808" + ], + "fragile nails": [ + "HP:0001808" + ], + "brittle nail": [ + "HP:0001808" + ], + "brittle nails": [ + "HP:0001808" + ], + "split nail": [ + "HP:0001809" + ], + "longitudinal splitting of nail": [ + "HP:0001809" + ], + "dystrophic toenail": [ + "HP:0001810" + ], + "dystrophic toenail change": [ + "HP:0001810" + ], + "dystrophic toenail changes": [ + "HP:0001810" + ], + "dystrophic toenails": [ + "HP:0001810" + ], + "poor toenail formation": [ + "HP:0001810" + ], + "hyperconvex fingernail": [ + "HP:0001812" + ], + "hyperconvex fingernails": [ + "HP:0001812" + ], + "tubular fingernail": [ + "HP:0001812" + ], + "tubular fingernails": [ + "HP:0001812" + ], + "deep - set nail": [ + "HP:0001814" + ], + "deep - set nails": [ + "HP:0001814" + ], + "thin nail": [ + "HP:0001816" + ], + "thin nails": [ + "HP:0001816" + ], + "absent fingernail": [ + "HP:0001817" + ], + "anonychia of fingernail": [ + "HP:0001817" + ], + "anonychia of fingernails": [ + "HP:0001817" + ], + "aplasia of the fingernail": [ + "HP:0001817" + ], + "paronychia": [ + "HP:0001818" + ], + "leukonychia": [ + "HP:0001820" + ], + "white discoloration of nail": [ + "HP:0001820" + ], + "white discoloration of nails": [ + "HP:0001820" + ], + "broad nail": [ + "HP:0001821" + ], + "broad fingernail": [ + "HP:0001821" + ], + "broad fingernails": [ + "HP:0001821" + ], + "wide fingernail": [ + "HP:0001821" + ], + "wide fingernails": [ + "HP:0001821" + ], + "hallux valgus": [ + "HP:0001822" + ], + "bunion": [ + "HP:0001822" + ], + "lateral deviation of great toe": [ + "HP:0001822" + ], + "lateral deviation of hallux": [ + "HP:0001822" + ], + "lateral deviation of halluces": [ + "HP:0001822" + ], + "weight loss": [ + "HP:0001824" + ], + "loss of weight": [ + "HP:0001824" + ], + "genital tract atresia": [ + "HP:0001827" + ], + "foot polydactyly": [ + "HP:0001829" + ], + "duplication of bone of the toe": [ + "HP:0001829" + ], + "duplication of bones of the toes": [ + "HP:0001829" + ], + "polydactyly of foot": [ + "HP:0001829" + ], + "polydactyly of feet": [ + "HP:0001829" + ], + "polydactyly of the foot": [ + "HP:0001829" + ], + "postaxial foot polydactyly": [ + "HP:0001830" + ], + "extra toe attach near the little toe": [ + "HP:0001830" + ], + "extra toe attached near the little toe": [ + "HP:0001830" + ], + "fibular polydactyly": [ + "HP:0001830" + ], + "polydactyly affect the 5th toe": [ + "HP:0001830" + ], + "polydactyly affecting the 5th toe": [ + "HP:0001830" + ], + "postaxial polydactyly of foot": [ + "HP:0001830" + ], + "postaxial polydactyly of feet": [ + "HP:0001830" + ], + "posterior polydactyly of foot": [ + "HP:0001830" + ], + "short toe": [ + "HP:0001831" + ], + "brachydactyly of the foot": [ + "HP:0001831" + ], + "hypoplasia of the toe": [ + "HP:0001831" + ], + "hypoplastic toe": [ + "HP:0001831" + ], + "hypoplastic toes": [ + "HP:0001831" + ], + "short foot phalanx": [ + "HP:0001831" + ], + "short foot phalanges": [ + "HP:0001831" + ], + "short toes": [ + "HP:0001831" + ], + "stubby toe": [ + "HP:0001831" + ], + "stubby toes": [ + "HP:0001831" + ], + "abnormal metatarsal morphology": [ + "HP:0001832" + ], + "abnormality of the long bone of foot": [ + "HP:0001832" + ], + "long foot": [ + "HP:0001833" + ], + "disproportionately large foot": [ + "HP:0001833" + ], + "disproportionately large feet": [ + "HP:0001833" + ], + "large foot": [ + "HP:0001833" + ], + "large feet": [ + "HP:0001833" + ], + "long feet": [ + "HP:0001833" + ], + "camptodactyly of toe": [ + "HP:0001836" + ], + "camptodactyly of foot": [ + "HP:0001836" + ], + "camptodactyly of feet": [ + "HP:0001836" + ], + "broad toe": [ + "HP:0001837" + ], + "wide toe": [ + "HP:0001837" + ], + "rocker bottom foot": [ + "HP:0001838" + ], + "congenital vertical talus": [ + "HP:0001838" + ], + "rocker bottom feet": [ + "HP:0001838" + ], + "rocker - bottom foot": [ + "HP:0001838" + ], + "rocker - bottom feet": [ + "HP:0001838" + ], + "rockerbottom foot": [ + "HP:0001838" + ], + "rockerbottom feet": [ + "HP:0001838" + ], + "split foot": [ + "HP:0001839" + ], + "foot ectrodactyly": [ + "HP:0001839" + ], + "lobster - claw foot deformity": [ + "HP:0001839" + ], + "split - foot": [ + "HP:0001839" + ], + "metatarsus adductus": [ + "HP:0001840" + ], + "forefoot varus": [ + "HP:0001840" + ], + "front half of foot turn inward": [ + "HP:0001840" + ], + "front half of foot turns inward": [ + "HP:0001840" + ], + "intoe": [ + "HP:0001840" + ], + "metatarsus adductovarsus": [ + "HP:0001840" + ], + "metatarsus varus": [ + "HP:0001840" + ], + "preaxial foot polydactyly": [ + "HP:0001841" + ], + "partial / complete duplication of the phalanx of the big toe": [ + "HP:0001841" + ], + "partial / complete duplication of the phalanges of the big toe": [ + "HP:0001841" + ], + "polydactyly affect the hallux": [ + "HP:0001841" + ], + "polydactyly affecting the hallux": [ + "HP:0001841" + ], + "preaxial hallucal polydactyly": [ + "HP:0001841" + ], + "preaxial polydactyly of foot": [ + "HP:0001841" + ], + "preaxial polydactyly of feet": [ + "HP:0001841" + ], + "preaxial polydactyly of the foot": [ + "HP:0001841" + ], + "preaxial polydactyly of the feet": [ + "HP:0001841" + ], + "preaxial polydactyly , foot": [ + "HP:0001841" + ], + "preaxial polydactyly , feet": [ + "HP:0001841" + ], + "foot acroosteolysis": [ + "HP:0001842" + ], + "acroosteolysis of foot": [ + "HP:0001842" + ], + "acroosteolysis of feet": [ + "HP:0001842" + ], + "abnormality of the hallux": [ + "HP:0001844" + ], + "abnormalities of the hallux": [ + "HP:0001844" + ], + "abnormality of the big toe": [ + "HP:0001844" + ], + "overlap toe": [ + "HP:0001845" + ], + "overlapping toe": [ + "HP:0001845" + ], + "crossover toe": [ + "HP:0001845" + ], + "overlapping toes": [ + "HP:0001845" + ], + "override toe": [ + "HP:0001845" + ], + "overriding toes": [ + "HP:0001845" + ], + "long hallux": [ + "HP:0001847" + ], + "increased length of the hallux": [ + "HP:0001847" + ], + "large hallux": [ + "HP:0001847" + ], + "large halluces": [ + "HP:0001847" + ], + "long big toe": [ + "HP:0001847" + ], + "long halluces": [ + "HP:0001847" + ], + "calcaneovalgus deformity": [ + "HP:0001848" + ], + "calcaneovalgus": [ + "HP:0001848" + ], + "calcaneovalgus foot": [ + "HP:0001848" + ], + "foot and ankle bend up toward shin of leg": [ + "HP:0001848" + ], + "valgus position of the calcaneus": [ + "HP:0001848" + ], + "foot oligodactyly": [ + "HP:0001849" + ], + "miss toe": [ + "HP:0001849" + ], + "missing toes": [ + "HP:0001849" + ], + "oligodactyly of foot": [ + "HP:0001849" + ], + "oligodactyly of feet": [ + "HP:0001849" + ], + "abnormality of the tarsal bone": [ + "HP:0001850" + ], + "abnormality of the tarsal bones": [ + "HP:0001850" + ], + "abnormal ankle bone": [ + "HP:0001850" + ], + "abnormal ankle bones": [ + "HP:0001850" + ], + "abnormal tarsal": [ + "HP:0001850" + ], + "abnormal tarsals": [ + "HP:0001850" + ], + "sandal gap": [ + "HP:0001852" + ], + "gap between 1st and 2nd toe": [ + "HP:0001852" + ], + "gap between 1st and 2nd toes": [ + "HP:0001852" + ], + "gap between first and second toe": [ + "HP:0001852" + ], + "increase space between first and second toe": [ + "HP:0001852" + ], + "increased space between first and second toes": [ + "HP:0001852" + ], + "sandal gap between first and second toe": [ + "HP:0001852" + ], + "sandal gap between first and second toes": [ + "HP:0001852" + ], + "space between great toe and second toe": [ + "HP:0001852" + ], + "wide space between 1st , 2nd toe": [ + "HP:0001852" + ], + "wide space between 1st , 2nd toes": [ + "HP:0001852" + ], + "wide space between first and second toe": [ + "HP:0001852" + ], + "wide space between first and second toes": [ + "HP:0001852" + ], + "wide - space big toe": [ + "HP:0001852" + ], + "wide - spaced big toe": [ + "HP:0001852" + ], + "widely space 1st - 2nd toe": [ + "HP:0001852" + ], + "widely spaced 1st - 2nd toes": [ + "HP:0001852" + ], + "widely space first and second toe": [ + "HP:0001852" + ], + "widely spaced first and second toes": [ + "HP:0001852" + ], + "widen gap 1st - 2nd toe": [ + "HP:0001852" + ], + "widened gap 1st - 2nd toes": [ + "HP:0001852" + ], + "widen gap first and second toe": [ + "HP:0001852" + ], + "widened gap first and second toe": [ + "HP:0001852" + ], + "bifid distal phalanx of toe": [ + "HP:0001853" + ], + "bifid distal phalanges of toes": [ + "HP:0001853" + ], + "bifid terminal phalanx of toe": [ + "HP:0001853" + ], + "notch outermost bone of toe": [ + "HP:0001853" + ], + "notched outermost bones of toes": [ + "HP:0001853" + ], + "podagra": [ + "HP:0001854" + ], + "gout of big toe": [ + "HP:0001854" + ], + "short distal phalanx of toe": [ + "HP:0001857" + ], + "hypoplastic distal phalanx of foot": [ + "HP:0001857" + ], + "hypoplastic distal phalanges of feet": [ + "HP:0001857" + ], + "short outermost bone of toe": [ + "HP:0001857" + ], + "distal foot symphalangism": [ + "HP:0001859" + ], + "obsolete acral ulceration and osteomyelitis lead to autoamputation of the digit ( foot )": [ + "HP:0001862" + ], + "obsolete acral ulceration and osteomyelitis leading to autoamputation of the digits ( feet )": [ + "HP:0001862" + ], + "toe clinodactyly": [ + "HP:0001863" + ], + "clinodactyly of foot": [ + "HP:0001863" + ], + "clinodactyly of feet": [ + "HP:0001863" + ], + "toe curvature": [ + "HP:0001863" + ], + "clinodactyly of the 5th toe": [ + "HP:0001864" + ], + "curvature of the little toe": [ + "HP:0001864" + ], + "curvature of the pinkie toe": [ + "HP:0001864" + ], + "curvature of the pinky toe": [ + "HP:0001864" + ], + "autoamputation of foot": [ + "HP:0001868" + ], + "deep plantar crease": [ + "HP:0001869" + ], + "deep plantar creases": [ + "HP:0001869" + ], + "deep wrinkle in sol of foot": [ + "HP:0001869" + ], + "deep wrinkles in soles of feet": [ + "HP:0001869" + ], + "acroosteolysis of distal phalanx ( foot )": [ + "HP:0001870" + ], + "acroosteolysis of distal phalanges ( feet )": [ + "HP:0001870" + ], + "acroosteolysis of distal phalanx of foot": [ + "HP:0001870" + ], + "acroosteolysis of distal phalanges of feet": [ + "HP:0001870" + ], + "abnormality of blood and blood - forming tissue": [ + "HP:0001871" + ], + "abnormality of blood and blood - forming tissues": [ + "HP:0001871" + ], + "abnormality of the haematopoietic system": [ + "HP:0001871" + ], + "abnormality of the hematopoietic system": [ + "HP:0001871" + ], + "haematological abnormality": [ + "HP:0001871" + ], + "hematologic disease": [ + "HP:0001871" + ], + "hematological abnormality": [ + "HP:0001871" + ], + "abnormal thrombocyte morphology": [ + "HP:0001872" + ], + "blood platelet disease": [ + "HP:0001872" + ], + "platelet abnormality": [ + "HP:0001872" + ], + "platelet abnormalities": [ + "HP:0001872" + ], + "thrombasthenia": [ + "HP:0001872" + ], + "thrombocytopenia": [ + "HP:0001873" + ], + "low platelet count": [ + "HP:0001873" + ], + "abnormality of neutrophil": [ + "HP:0001874" + ], + "abnormality of neutrophils": [ + "HP:0001874" + ], + "abnormality of polymorphonuclear neutrophil": [ + "HP:0001874" + ], + "abnormality of polymorphonuclear neutrophils": [ + "HP:0001874" + ], + "neutropenia": [ + "HP:0001875" + ], + "low blood neutrophil count": [ + "HP:0001875" + ], + "low neutrophil count": [ + "HP:0001875" + ], + "neutropoenia": [ + "HP:0001875" + ], + "peripheral neutropenia": [ + "HP:0001875" + ], + "pancytopenia": [ + "HP:0001876" + ], + "low blood cell count": [ + "HP:0001876" + ], + "pancytopaenia": [ + "HP:0001876" + ], + "abnormal erythrocyte morphology": [ + "HP:0001877" + ], + "abnormality of erythrocyte": [ + "HP:0001877" + ], + "abnormality of erythrocytes": [ + "HP:0001877" + ], + "abnormality of erythroid lineage cell": [ + "HP:0001877" + ], + "abnormality of red blood cell": [ + "HP:0001877" + ], + "abnormality of red blood cells": [ + "HP:0001877" + ], + "hemolytic anemia": [ + "HP:0001878" + ], + "haemolytic anaemia": [ + "HP:0001878" + ], + "hemolytic anaemia": [ + "HP:0001878" + ], + "increase hemolysis": [ + "HP:0001878" + ], + "increased hemolysis": [ + "HP:0001878" + ], + "abnormal eosinophil morphology": [ + "HP:0001879" + ], + "abnormality of eosinophil": [ + "HP:0001879" + ], + "abnormality of eosinophils": [ + "HP:0001879" + ], + "eosinophilia": [ + "HP:0001880" + ], + "high blood eosinophil count": [ + "HP:0001880" + ], + "abnormal leukocyte morphology": [ + "HP:0001881" + ], + "abnormality of leukocyte": [ + "HP:0001881" + ], + "abnormality of leukocytes": [ + "HP:0001881" + ], + "leukopenia": [ + "HP:0001882" + ], + "decrease blood leukocyte number": [ + "HP:0001882" + ], + "decreased blood leukocyte number": [ + "HP:0001882" + ], + "low white blood cell count": [ + "HP:0001882" + ], + "talipes": [ + "HP:0001883" + ], + "talipes foot deformity": [ + "HP:0001883" + ], + "talipes foot deformities": [ + "HP:0001883" + ], + "talipes calcaneovalgus": [ + "HP:0001884" + ], + "pe calcaneovarus": [ + "HP:0001884" + ], + "pes calcaneovarus": [ + "HP:0001884" + ], + "short 2nd toe": [ + "HP:0001885" + ], + "short second toe": [ + "HP:0001885" + ], + "foot osteomyelitis": [ + "HP:0001886" + ], + "foot bone infection": [ + "HP:0001886" + ], + "lymphopenia": [ + "HP:0001888" + ], + "absolute lymphocyte count decrease": [ + "HP:0001888" + ], + "decrease blood lymphocyte number": [ + "HP:0001888" + ], + "decreased blood lymphocyte number": [ + "HP:0001888" + ], + "low lymphocyte number": [ + "HP:0001888" + ], + "lymphocytopenia": [ + "HP:0001888" + ], + "megaloblastic anemia": [ + "HP:0001889" + ], + "megaloblastic anaemia": [ + "HP:0001889" + ], + "autoimmune hemolytic anemia": [ + "HP:0001890" + ], + "autoimmune haemolytic anaemia": [ + "HP:0001890" + ], + "autoimmune hemolytic anaemia": [ + "HP:0001890" + ], + "hemolytic anemia , autoimmune": [ + "HP:0001890" + ], + "iron deficiency anemia": [ + "HP:0001891" + ], + "ferropenic": [ + "HP:0001891" + ], + "iron deficiency anaemia": [ + "HP:0001891" + ], + "iron - deficiency anaemia": [ + "HP:0001891" + ], + "iron - deficiency anemia": [ + "HP:0001891" + ], + "abnormal bleeding": [ + "HP:0001892" + ], + "bleed diathesis": [ + "HP:0001892" + ], + "bleeding diathesis": [ + "HP:0001892" + ], + "bleeding tendency": [ + "HP:0001892" + ], + "hemorrhagic diathesis": [ + "HP:0001892" + ], + "thrombocytosis": [ + "HP:0001894" + ], + "increased number of platelet in blood": [ + "HP:0001894" + ], + "increased number of platelets in blood": [ + "HP:0001894" + ], + "increase platelet count": [ + "HP:0001894" + ], + "increased platelet count": [ + "HP:0001894" + ], + "thrombocythaemia": [ + "HP:0001894" + ], + "thrombocythemia": [ + "HP:0001894" + ], + "normochromic anemia": [ + "HP:0001895" + ], + "normochromic anaemia": [ + "HP:0001895" + ], + "reticulocytopenia": [ + "HP:0001896" + ], + "normocytic anemia": [ + "HP:0001897" + ], + "normocytic anaemia": [ + "HP:0001897" + ], + "increase red blood cell mass": [ + "HP:0001898" + ], + "increased red blood cell mass": [ + "HP:0001898" + ], + "increase rbc mass": [ + "HP:0001898" + ], + "increased rbc mass": [ + "HP:0001898" + ], + "increase hematocrit": [ + "HP:0001899" + ], + "increased hematocrit": [ + "HP:0001899" + ], + "increase hct": [ + "HP:0001899" + ], + "increased hct": [ + "HP:0001899" + ], + "increase hemoglobin": [ + "HP:0001900" + ], + "increased hemoglobin": [ + "HP:0001900" + ], + "increase haemoglobin": [ + "HP:0001900" + ], + "increased haemoglobin": [ + "HP:0001900" + ], + "increase hb": [ + "HP:0001900" + ], + "increased hb": [ + "HP:0001900" + ], + "polycythemia": [ + "HP:0001901" + ], + "abnormally shape erythrocyte": [ + "HP:0001901" + ], + "abnormally shaped erythrocytes": [ + "HP:0001901" + ], + "erythrocytosis": [ + "HP:0001901" + ], + "increase red blood cell": [ + "HP:0001901" + ], + "increased red blood cells": [ + "HP:0001901" + ], + "polyglobulia": [ + "HP:0001901" + ], + "giant platelet": [ + "HP:0001902" + ], + "giant platelets": [ + "HP:0001902" + ], + "anemia": [ + "HP:0001903" + ], + "anaemia": [ + "HP:0001903" + ], + "decrease haemoglobin": [ + "HP:0001903" + ], + "decreased haemoglobin": [ + "HP:0001903" + ], + "decrease hemoglobin": [ + "HP:0001903" + ], + "decreased hemoglobin": [ + "HP:0001903" + ], + "low number of red blood cell or haemoglobin": [ + "HP:0001903" + ], + "low number of red blood cells or haemoglobin": [ + "HP:0001903" + ], + "low number of red blood cell or hemoglobin": [ + "HP:0001903" + ], + "low number of red blood cells or hemoglobin": [ + "HP:0001903" + ], + "neutropenia in presence of anti - neutropil antibody": [ + "HP:0001904" + ], + "neutropenia in presence of anti - neutropil antibodies": [ + "HP:0001904" + ], + "autoimmune neutropenia": [ + "HP:0001904" + ], + "congenital thrombocytopenia": [ + "HP:0001905" + ], + "thrombocytopenia , congenital": [ + "HP:0001905" + ], + "thromboembolism": [ + "HP:0001907" + ], + "blood clot in blood vessel": [ + "HP:0001907" + ], + "embolism and thrombosis": [ + "HP:0001907" + ], + "thromboembolic disease": [ + "HP:0001907" + ], + "thromboembolic event": [ + "HP:0001907" + ], + "thromboembolic events": [ + "HP:0001907" + ], + "hypoplastic anemia": [ + "HP:0001908" + ], + "hypoplastic anaemia": [ + "HP:0001908" + ], + "leukemia": [ + "HP:0001909" + ], + "blood cancer": [ + "HP:0001909" + ], + "leukaemia": [ + "HP:0001909" + ], + "abnormal granulocyte morphology": [ + "HP:0001911" + ], + "abnormality of granulocyte": [ + "HP:0001911" + ], + "abnormality of granulocytes": [ + "HP:0001911" + ], + "abnormal basophil morphology": [ + "HP:0001912" + ], + "abnormality of basophil": [ + "HP:0001912" + ], + "abnormality of basophils": [ + "HP:0001912" + ], + "granulocytopenia": [ + "HP:0001913" + ], + "aplastic anemia": [ + "HP:0001915" + ], + "aplastic anaemia": [ + "HP:0001915" + ], + "renal amyloidosis": [ + "HP:0001917" + ], + "acute kidney injury": [ + "HP:0001919" + ], + "acute kidney failure": [ + "HP:0001919" + ], + "acute renal failure": [ + "HP:0001919" + ], + "renal artery stenosis": [ + "HP:0001920" + ], + "narrowing of kidney artery": [ + "HP:0001920" + ], + "vacuolated lymphocyte": [ + "HP:0001922" + ], + "vacuolated lymphocytes": [ + "HP:0001922" + ], + "enlarge lysosomal vacuole in lymphocyte": [ + "HP:0001922" + ], + "enlarged lysosomal vacuoles in lymphocytes": [ + "HP:0001922" + ], + "vacuolated blood lymphocyte": [ + "HP:0001922" + ], + "vacuolated blood lymphocytes": [ + "HP:0001922" + ], + "reticulocytosis": [ + "HP:0001923" + ], + "increased immature red blood cell": [ + "HP:0001923" + ], + "increased immature red blood cells": [ + "HP:0001923" + ], + "increased number of immature red blood cell": [ + "HP:0001923" + ], + "increased number of immature red blood cells": [ + "HP:0001923" + ], + "increase reticulocyte count": [ + "HP:0001923" + ], + "increased reticulocyte count": [ + "HP:0001923" + ], + "increase reticulocyte": [ + "HP:0001923" + ], + "increased reticulocytes": [ + "HP:0001923" + ], + "polychromasia": [ + "HP:0001923" + ], + "sideroblastic anemia": [ + "HP:0001924" + ], + "hypersideremic anaemia": [ + "HP:0001924" + ], + "hypersideremic anemia": [ + "HP:0001924" + ], + "sideroblastic anaemia": [ + "HP:0001924" + ], + "acanthocytosis": [ + "HP:0001927" + ], + "acanthocyte": [ + "HP:0001927" + ], + "acanthocytes": [ + "HP:0001927" + ], + "red cell acanthocytosis": [ + "HP:0001927" + ], + "abnormality of coagulation": [ + "HP:0001928" + ], + "abnormal blood coagulation study": [ + "HP:0001928" + ], + "abnormal blood coagulation studies": [ + "HP:0001928" + ], + "blood coagulation disorder": [ + "HP:0001928" + ], + "coagulation abnormality": [ + "HP:0001928" + ], + "coagulation abnormalities": [ + "HP:0001928" + ], + "haemorrhagic disorder": [ + "HP:0001928" + ], + "haemorrhagic disorders": [ + "HP:0001928" + ], + "reduce factor xi activity": [ + "HP:0001929" + ], + "reduced factor xi activity": [ + "HP:0001929" + ], + "factor xi deficiency": [ + "HP:0001929" + ], + "low factor xi activity": [ + "HP:0001929" + ], + "nonspherocytic hemolytic anemia": [ + "HP:0001930" + ], + "nonspherocytic hemolytic anaemia": [ + "HP:0001930" + ], + "hypochromic anemia": [ + "HP:0001931" + ], + "hypochromic anaemia": [ + "HP:0001931" + ], + "subcutaneous hemorrhage": [ + "HP:0001933" + ], + "bleed below the skin": [ + "HP:0001933" + ], + "bleeding below the skin": [ + "HP:0001933" + ], + "subcutaneous haemorrhage": [ + "HP:0001933" + ], + "persistent bleeding after trauma": [ + "HP:0001934" + ], + "excessive bleeding after minor trauma": [ + "HP:0001934" + ], + "frequent bleed with trauma": [ + "HP:0001934" + ], + "frequent bleeding with trauma": [ + "HP:0001934" + ], + "prolong bleeding after minor trauma": [ + "HP:0001934" + ], + "prolonged bleeding after minor trauma": [ + "HP:0001934" + ], + "microcytic anemia": [ + "HP:0001935" + ], + "microcytic anaemia": [ + "HP:0001935" + ], + "microangiopathic hemolytic anemia": [ + "HP:0001937" + ], + "microangiopathic hemolytic anaemia": [ + "HP:0001937" + ], + "abnormality of metabolism / homeostasis": [ + "HP:0001939" + ], + "laboratory abnormality": [ + "HP:0001939" + ], + "metabolism abnormality": [ + "HP:0001939" + ], + "acidosis": [ + "HP:0001941" + ], + "metabolic acidosis": [ + "HP:0001942" + ], + "hypoglycemia": [ + "HP:0001943" + ], + "hypoglycaemia": [ + "HP:0001943" + ], + "low blood sugar": [ + "HP:0001943" + ], + "dehydration": [ + "HP:0001944" + ], + "exsiccosis": [ + "HP:0001944" + ], + "fever": [ + "HP:0001945" + ], + "hyperthermia": [ + "HP:0001945" + ], + "pyrexia": [ + "HP:0001945" + ], + "ketosis": [ + "HP:0001946" + ], + "high level of ketone body": [ + "HP:0001946" + ], + "high levels of ketone bodies": [ + "HP:0001946" + ], + "hyperketosis": [ + "HP:0001946" + ], + "renal tubular acidosis": [ + "HP:0001947" + ], + "accumulation of acid in body due to kidney problem": [ + "HP:0001947" + ], + "alkalosis": [ + "HP:0001948" + ], + "hypokalemic alkalosis": [ + "HP:0001949" + ], + "respiratory alkalosis": [ + "HP:0001950" + ], + "episodic ammonia intoxication": [ + "HP:0001951" + ], + "glucose intolerance": [ + "HP:0001952" + ], + "abnormal glucose tolerance": [ + "HP:0001952" + ], + "diabetic ketoacidosis": [ + "HP:0001953" + ], + "diabetic ketosis": [ + "HP:0001953" + ], + "recurrent fever": [ + "HP:0001954" + ], + "episodic fever": [ + "HP:0001954" + ], + "hyperthermia , episodic": [ + "HP:0001954" + ], + "increase body temperature , episodic": [ + "HP:0001954" + ], + "increased body temperature , episodic": [ + "HP:0001954" + ], + "intermittent fever": [ + "HP:0001954" + ], + "unexplained fever": [ + "HP:0001955" + ], + "unexplained fevers": [ + "HP:0001955" + ], + "truncal obesity": [ + "HP:0001956" + ], + "centripetal obesity": [ + "HP:0001956" + ], + "nonketotic hypoglycemia": [ + "HP:0001958" + ], + "polydipsia": [ + "HP:0001959" + ], + "extreme thirst": [ + "HP:0001959" + ], + "hypokalemic metabolic alkalosis": [ + "HP:0001960" + ], + "hypoplastic heart": [ + "HP:0001961" + ], + "small heart": [ + "HP:0001961" + ], + "underdeveloped heart": [ + "HP:0001961" + ], + "palpitation": [ + "HP:0001962" + ], + "palpitations": [ + "HP:0001962" + ], + "heart palpitation": [ + "HP:0001962" + ], + "heart palpitations": [ + "HP:0001962" + ], + "missed heart beat": [ + "HP:0001962" + ], + "skipped heart beat": [ + "HP:0001962" + ], + "abnormal speech discrimination": [ + "HP:0001963" + ], + "poor speech discrimination": [ + "HP:0001963" + ], + "aplasia / hypoplasia of metatarsal bone": [ + "HP:0001964" + ], + "aplasia / hypoplasia of metatarsal bones": [ + "HP:0001964" + ], + "absent or hypoplastic metatarsal": [ + "HP:0001964" + ], + "absent / hypoplastic metacarpal": [ + "HP:0001964" + ], + "absent / hypoplastic metacarpals": [ + "HP:0001964" + ], + "absent / hypoplastic metatarsal": [ + "HP:0001964" + ], + "absent / hypoplastic metatarsals": [ + "HP:0001964" + ], + "absent / small long bone of foot": [ + "HP:0001964" + ], + "absent / underdevelop long bone of foot": [ + "HP:0001964" + ], + "absent / underdeveloped long bone of foot": [ + "HP:0001964" + ], + "aplastic / hypoplastic metatarsal": [ + "HP:0001964" + ], + "aplastic / hypoplastic metatarsals": [ + "HP:0001964" + ], + "abnormal scalp morphology": [ + "HP:0001965" + ], + "abnormality of the scalp": [ + "HP:0001965" + ], + "anomaly of scalp": [ + "HP:0001965" + ], + "abnormal glomerular mesangium morphology": [ + "HP:0001966" + ], + "abnormality glomerular mesangium morphology": [ + "HP:0001966" + ], + "abnormality of the glomerular mesangium": [ + "HP:0001966" + ], + "mesangial abnormality": [ + "HP:0001966" + ], + "diffuse mesangial sclerosis": [ + "HP:0001967" + ], + "diffuse mesangial sclerosis glomerulopathy": [ + "HP:0001967" + ], + "mesangial sclerosis": [ + "HP:0001967" + ], + "abnormal tubulointerstitial morphology": [ + "HP:0001969" + ], + "tubulointerstitial abnormality": [ + "HP:0001969" + ], + "tubulointerstitial nephropathy": [ + "HP:0001969" + ], + "tubulointerstitial nephritis": [ + "HP:0001970" + ], + "interstitial nephritis": [ + "HP:0001970" + ], + "nephritis , tubulointerstitial": [ + "HP:0001970" + ], + "hypersplenism": [ + "HP:0001971" + ], + "macrocytic anemia": [ + "HP:0001972" + ], + "macrocytic anaemia": [ + "HP:0001972" + ], + "autoimmune thrombocytopenia": [ + "HP:0001973" + ], + "idiopathic thrombocytopenia": [ + "HP:0001973" + ], + "idiopathic thrombocytopenic purpura": [ + "HP:0001973" + ], + "immune thrombocytopenia": [ + "HP:0001973" + ], + "leukocytosis": [ + "HP:0001974" + ], + "elevate white blood count": [ + "HP:0001974" + ], + "elevated white blood count": [ + "HP:0001974" + ], + "high white blood count": [ + "HP:0001974" + ], + "increase blood leukocyte number": [ + "HP:0001974" + ], + "increased blood leukocyte number": [ + "HP:0001974" + ], + "decrease platelet glycoprotein iib - iiia": [ + "HP:0001975" + ], + "decreased platelet glycoprotein iib - iiia": [ + "HP:0001975" + ], + "glanzmann thrombasthenia": [ + "HP:0001975" + ], + "reduce level of platelet glycoprotein iib / iiia complex": [ + "HP:0001975" + ], + "reduced level of platelet glycoprotein iib / iiia complex": [ + "HP:0001975" + ], + "reduce antithrombin iii activity": [ + "HP:0001976" + ], + "reduced antithrombin iii activity": [ + "HP:0001976" + ], + "anti - thrombin iii deficiency": [ + "HP:0001976" + ], + "antithrombin iii deficiency": [ + "HP:0001976" + ], + "decrease antithrombin iii": [ + "HP:0001976" + ], + "decreased antithrombin iii": [ + "HP:0001976" + ], + "abnormal thrombosis": [ + "HP:0001977" + ], + "abnormal blood clot": [ + "HP:0001977" + ], + "abnormal blood clotting": [ + "HP:0001977" + ], + "extramedullary hematopoiesis": [ + "HP:0001978" + ], + "extramedullary erythropoiesis": [ + "HP:0001978" + ], + "megaloblastic bone marrow": [ + "HP:0001980" + ], + "schistocytosis": [ + "HP:0001981" + ], + "schistocytes": [ + "HP:0001981" + ], + "sea - blue histiocytosis": [ + "HP:0001982" + ], + "'sea blue ' histiocyte": [ + "HP:0001982" + ], + "'sea blue ' histiocytes": [ + "HP:0001982" + ], + "sea - blue histiocyte": [ + "HP:0001982" + ], + "reduce lymphocyte surface expression of cd43": [ + "HP:0001983" + ], + "reduced lymphocyte surface expression of cd43": [ + "HP:0001983" + ], + "cd43 defectively express on surface of blood cell": [ + "HP:0001983" + ], + "cd43 defectively expressed on surface of blood cells": [ + "HP:0001983" + ], + "reduce lymphocyte surface expression of sialophorin": [ + "HP:0001983" + ], + "reduced lymphocyte surface expression of sialophorin": [ + "HP:0001983" + ], + "intolerance to protein": [ + "HP:0001984" + ], + "hypoketotic hypoglycemia": [ + "HP:0001985" + ], + "hypoglycemia , hypoketotic": [ + "HP:0001985" + ], + "hypertonic dehydration": [ + "HP:0001986" + ], + "hyperosmolar dehydration": [ + "HP:0001986" + ], + "hyperammonemia": [ + "HP:0001987" + ], + "high blood ammonia level": [ + "HP:0001987" + ], + "high blood ammonia levels": [ + "HP:0001987" + ], + "recurrent hypoglycemia": [ + "HP:0001988" + ], + "hypoglycaemia , recurrent": [ + "HP:0001988" + ], + "hypoglycemia , recurrent": [ + "HP:0001988" + ], + "hypoglycemic episode": [ + "HP:0001988" + ], + "hypoglycemic episodes": [ + "HP:0001988" + ], + "recurrent hypoglycaemia": [ + "HP:0001988" + ], + "recurrent hypoglycemic episode": [ + "HP:0001988" + ], + "recurrent hypoglycemic episodes": [ + "HP:0001988" + ], + "recurrent low blood sugar level": [ + "HP:0001988" + ], + "recurrent low blood sugar levels": [ + "HP:0001988" + ], + "fetal akinesia sequence": [ + "HP:0001989" + ], + "early severe fetal akinesia sequence": [ + "HP:0001989" + ], + "early severe foetal akinesia sequence": [ + "HP:0001989" + ], + "fetal akinesia": [ + "HP:0001989" + ], + "foetal akinesia": [ + "HP:0001989" + ], + "foetal akinesia sequence": [ + "HP:0001989" + ], + "aplasia / hypoplasia of toe": [ + "HP:0001991" + ], + "absent / hypoplastic toe": [ + "HP:0001991" + ], + "absent / hypoplastic toes": [ + "HP:0001991" + ], + "absent / small toe": [ + "HP:0001991" + ], + "absent / underdevelop toe": [ + "HP:0001991" + ], + "absent / underdeveloped toe": [ + "HP:0001991" + ], + "aplastic / hypoplastic toe phalanx": [ + "HP:0001991" + ], + "aplastic / hypoplastic toe phalanges": [ + "HP:0001991" + ], + "organic aciduria": [ + "HP:0001992" + ], + "ketoacidosis": [ + "HP:0001993" + ], + "renal fanconi syndrome": [ + "HP:0001994" + ], + "'de toni - fanconi - debre ' syndrome": [ + "HP:0001994" + ], + "renal tubular fanconi syndrome": [ + "HP:0001994" + ], + "hyperchloremic acidosis": [ + "HP:0001995" + ], + "chronic metabolic acidosis": [ + "HP:0001996" + ], + "gout": [ + "HP:0001997" + ], + "gouty arthritis": [ + "HP:0001997" + ], + "neonatal hypoglycemia": [ + "HP:0001998" + ], + "low blood sugar in newborn": [ + "HP:0001998" + ], + "abnormal facial shape": [ + "HP:0001999" + ], + "abnormal morphology of the face": [ + "HP:0001999" + ], + "deformity of face": [ + "HP:0001999" + ], + "distinctive facies": [ + "HP:0001999" + ], + "distortion of face": [ + "HP:0001999" + ], + "dysmorphic facial feature": [ + "HP:0001999" + ], + "dysmorphic facial features": [ + "HP:0001999" + ], + "dysmorphic facies": [ + "HP:0001999" + ], + "facial dysmorphism": [ + "HP:0001999" + ], + "funny look face": [ + "HP:0001999" + ], + "funny looking face": [ + "HP:0001999" + ], + "malformation of face": [ + "HP:0001999" + ], + "unusual facial appearance": [ + "HP:0001999" + ], + "unusual facies": [ + "HP:0001999" + ], + "short columella": [ + "HP:0002000" + ], + "columella , short": [ + "HP:0002000" + ], + "decreased length of columella": [ + "HP:0002000" + ], + "hypoplasia of columella": [ + "HP:0002000" + ], + "deep philtrum": [ + "HP:0002002" + ], + "depressed philtrum": [ + "HP:0002002" + ], + "increase depth of philtrum": [ + "HP:0002002" + ], + "increased depth of philtrum": [ + "HP:0002002" + ], + "philtrum , deep": [ + "HP:0002002" + ], + "prominent philtrum": [ + "HP:0002002" + ], + "pronounce philtrum": [ + "HP:0002002" + ], + "pronounced philtrum": [ + "HP:0002002" + ], + "large forehead": [ + "HP:0002003" + ], + "hyperplasia of forehead": [ + "HP:0002003" + ], + "hypertrophy of forehead": [ + "HP:0002003" + ], + "increase size of forehead": [ + "HP:0002003" + ], + "increased size of forehead": [ + "HP:0002003" + ], + "increase size of frontal region of face": [ + "HP:0002003" + ], + "increased size of frontal region of face": [ + "HP:0002003" + ], + "facial cleft": [ + "HP:0002006" + ], + "cleft of the face": [ + "HP:0002006" + ], + "facial clefts": [ + "HP:0002006" + ], + "tessier facial cleft": [ + "HP:0002006" + ], + "frontal bossing": [ + "HP:0002007" + ], + "frontal protruberance": [ + "HP:0002007" + ], + "skull bossing": [ + "HP:0002007" + ], + "potter facies": [ + "HP:0002009" + ], + "narrow maxilla": [ + "HP:0002010" + ], + "decrease breadth of upper jaw bone": [ + "HP:0002010" + ], + "decreased breadth of upper jaw bones": [ + "HP:0002010" + ], + "decreased transverse dimension of maxilla": [ + "HP:0002010" + ], + "decrease width of maxilla": [ + "HP:0002010" + ], + "decreased width of maxilla": [ + "HP:0002010" + ], + "decrease width of upper jaw bone": [ + "HP:0002010" + ], + "decreased width of upper jaw bones": [ + "HP:0002010" + ], + "narrow upper jaw bone": [ + "HP:0002010" + ], + "narrow upper jaw bones": [ + "HP:0002010" + ], + "transverse hypoplasia of maxilla": [ + "HP:0002010" + ], + "transverse maxillary deficiency": [ + "HP:0002010" + ], + "transverse maxillary insufficiency": [ + "HP:0002010" + ], + "morphological central nervous system abnormality": [ + "HP:0002011" + ], + "abnormality of the central nervous system": [ + "HP:0002011" + ], + "central nervous system disease": [ + "HP:0002011" + ], + "morphological abnormality of the central nervous system": [ + "HP:0002011" + ], + "morphological abnormality of the cns": [ + "HP:0002011" + ], + "abnormality of the abdominal organ": [ + "HP:0002012" + ], + "abnormality of the abdominal organs": [ + "HP:0002012" + ], + "gastrointestinal tract defect": [ + "HP:0002012" + ], + "gastrointestinal tract defects": [ + "HP:0002012" + ], + "vomit": [ + "HP:0002013" + ], + "vomiting": [ + "HP:0002013" + ], + "emesis": [ + "HP:0002013" + ], + "throw up": [ + "HP:0002013" + ], + "throwing up": [ + "HP:0002013" + ], + "diarrhea": [ + "HP:0002014" + ], + "diarrhoea": [ + "HP:0002014" + ], + "watery stool": [ + "HP:0002014" + ], + "dysphagia": [ + "HP:0002015" + ], + "deglutition disorder": [ + "HP:0002015" + ], + "difficulty swallow": [ + "HP:0002015" + ], + "difficulty swallowing": [ + "HP:0002015" + ], + "poor swallowing": [ + "HP:0002015" + ], + "swallow difficulty": [ + "HP:0002015" + ], + "swallowing difficulties": [ + "HP:0002015" + ], + "swallowing difficulty": [ + "HP:0002015" + ], + "nausea and vomiting": [ + "HP:0002017" + ], + "nausea": [ + "HP:0002018" + ], + "constipation": [ + "HP:0002019" + ], + "costiveness": [ + "HP:0002019" + ], + "dyschezia": [ + "HP:0002019" + ], + "gastroesophageal reflux": [ + "HP:0002020" + ], + "acid reflux": [ + "HP:0002020" + ], + "acid reflux disease": [ + "HP:0002020" + ], + "gastro - esophageal reflux": [ + "HP:0002020" + ], + "gastro - oesophageal reflux": [ + "HP:0002020" + ], + "gastroesophageal reflux disease": [ + "HP:0002020" + ], + "heartburn": [ + "HP:0002020" + ], + "pyloric stenosis": [ + "HP:0002021" + ], + "anal atresia": [ + "HP:0002023" + ], + "absent anus": [ + "HP:0002023" + ], + "imperforate anus": [ + "HP:0002023" + ], + "malabsorption": [ + "HP:0002024" + ], + "intestinal malabsorption": [ + "HP:0002024" + ], + "anal stenosis": [ + "HP:0002025" + ], + "narrowing of anal opening": [ + "HP:0002025" + ], + "abdominal pain": [ + "HP:0002027" + ], + "abdominal discomfort": [ + "HP:0002027" + ], + "gastro pain": [ + "HP:0002027" + ], + "gastrointestinal pain": [ + "HP:0002027" + ], + "pain in stomach": [ + "HP:0002027" + ], + "stomach pain": [ + "HP:0002027" + ], + "upset stomach": [ + "HP:0002027" + ], + "chronic diarrhea": [ + "HP:0002028" + ], + "chronic diarrhoea": [ + "HP:0002028" + ], + "diarrhea , recurrent": [ + "HP:0002028" + ], + "recurrent diarrhea": [ + "HP:0002028" + ], + "recurrent diarrhoea": [ + "HP:0002028" + ], + "abnormal esophagus morphology": [ + "HP:0002031" + ], + "abnormal oesophagus morphology": [ + "HP:0002031" + ], + "abnormality of esophagus structure": [ + "HP:0002031" + ], + "abnormality of oesophagus structure": [ + "HP:0002031" + ], + "anomaly of the esophagus": [ + "HP:0002031" + ], + "anomaly of the oesophagus": [ + "HP:0002031" + ], + "esophageal atresia": [ + "HP:0002032" + ], + "birth defect in which part of esophagus do not develop": [ + "HP:0002032" + ], + "birth defect in which part of esophagus did not develop": [ + "HP:0002032" + ], + "birth defect in which part of oesophagus do not develop": [ + "HP:0002032" + ], + "birth defect in which part of oesophagus did not develop": [ + "HP:0002032" + ], + "poor suck": [ + "HP:0002033" + ], + "poor sucking": [ + "HP:0002033" + ], + "suck weakness": [ + "HP:0002033" + ], + "sucking weakness": [ + "HP:0002033" + ], + "abnormal rectum morphology": [ + "HP:0002034" + ], + "abnormality of the rectum": [ + "HP:0002034" + ], + "anomaly of the rectum": [ + "HP:0002034" + ], + "rectal prolapse": [ + "HP:0002035" + ], + "rectal prolapsed": [ + "HP:0002035" + ], + "rectum protrudes through anus": [ + "HP:0002035" + ], + "hiatus hernia": [ + "HP:0002036" + ], + "hiatal hernia": [ + "HP:0002036" + ], + "stomach hernia": [ + "HP:0002036" + ], + "inflammation of the large intestine": [ + "HP:0002037" + ], + "inflammatory bowel disease": [ + "HP:0002037" + ], + "protein avoidance": [ + "HP:0002038" + ], + "anorexia": [ + "HP:0002039" + ], + "esophageal varix": [ + "HP:0002040" + ], + "enlarge vein in esophagus": [ + "HP:0002040" + ], + "enlarged vein in esophagus": [ + "HP:0002040" + ], + "enlarge vein in oesophagus": [ + "HP:0002040" + ], + "enlarged vein in oesophagus": [ + "HP:0002040" + ], + "esophageal varices": [ + "HP:0002040" + ], + "intractable diarrhea": [ + "HP:0002041" + ], + "intractable diarrhoea": [ + "HP:0002041" + ], + "esophageal stricture": [ + "HP:0002043" + ], + "narrowing of esophagus due to inflammation and scar tissue": [ + "HP:0002043" + ], + "narrowing of oesophagus due to inflammation and scar tissue": [ + "HP:0002043" + ], + "zollinger - ellison syndrome": [ + "HP:0002044" + ], + "hypothermia": [ + "HP:0002045" + ], + "abnormally low body temperature": [ + "HP:0002045" + ], + "heat intolerance": [ + "HP:0002046" + ], + "intolerance to heat and fever": [ + "HP:0002046" + ], + "intolerance to heat and fevers": [ + "HP:0002046" + ], + "malignant hyperthermia": [ + "HP:0002047" + ], + "malignant hyperthermia with anaesthesia": [ + "HP:0002047" + ], + "malignant hyperthermia with anesthesia": [ + "HP:0002047" + ], + "renal cortical atrophy": [ + "HP:0002048" + ], + "proximal renal tubular acidosis": [ + "HP:0002049" + ], + "proximal tubular acidosis": [ + "HP:0002049" + ], + "renal tubular acidosis , proximal": [ + "HP:0002049" + ], + "renal tubular acidosis , type ii": [ + "HP:0002049" + ], + "macroorchidism , postpubertal": [ + "HP:0002050" + ], + "heavy supraorbital ridge": [ + "HP:0002054" + ], + "heavy supraorbital ridges": [ + "HP:0002054" + ], + "heavy brow of the face": [ + "HP:0002054" + ], + "curve linear dimple below the low lip": [ + "HP:0002055" + ], + "curved linear dimple below the lower lip": [ + "HP:0002055" + ], + "abnormality of the glabella": [ + "HP:0002056" + ], + "abnormality of the area between the eyebrow": [ + "HP:0002056" + ], + "abnormality of the area between the eyebrows": [ + "HP:0002056" + ], + "deformity of the area between the eyebrow": [ + "HP:0002056" + ], + "deformity of the area between the eyebrows": [ + "HP:0002056" + ], + "glabellar abnormality": [ + "HP:0002056" + ], + "malformation of the area between the eyebrow": [ + "HP:0002056" + ], + "malformation of the area between the eyebrows": [ + "HP:0002056" + ], + "prominent glabella": [ + "HP:0002057" + ], + "convex glabella": [ + "HP:0002057" + ], + "hyperplasia of glabella": [ + "HP:0002057" + ], + "prominent area between the eyebrow": [ + "HP:0002057" + ], + "prominent area between the eyebrows": [ + "HP:0002057" + ], + "protrude area between the eyebrow": [ + "HP:0002057" + ], + "protruding area between the eyebrows": [ + "HP:0002057" + ], + "myopathic facies": [ + "HP:0002058" + ], + "myopathic face": [ + "HP:0002058" + ], + "myopathic facial appearance": [ + "HP:0002058" + ], + "cerebral atrophy": [ + "HP:0002059" + ], + "degeneration of cerebrum": [ + "HP:0002059" + ], + "supratentorial atrophy": [ + "HP:0002059" + ], + "abnormal cerebral morphology": [ + "HP:0002060" + ], + "abnormality of the cerebrum": [ + "HP:0002060" + ], + "abnormality of the telencephalon": [ + "HP:0002060" + ], + "cerebral lesion": [ + "HP:0002060" + ], + "low limb spasticity": [ + "HP:0002061" + ], + "lower limb spasticity": [ + "HP:0002061" + ], + "morphological abnormality of the pyramidal tract": [ + "HP:0002062" + ], + "abnormality of the pyramidal tract": [ + "HP:0002062" + ], + "abnormality of the pyramidal tracts": [ + "HP:0002062" + ], + "pyramidal tract disease": [ + "HP:0002062" + ], + "rigidity": [ + "HP:0002063" + ], + "muscle rigidity": [ + "HP:0002063" + ], + "spastic gait": [ + "HP:0002064" + ], + "spastic walk": [ + "HP:0002064" + ], + "gait ataxia": [ + "HP:0002066" + ], + "ataxia of gait": [ + "HP:0002066" + ], + "ataxic gait": [ + "HP:0002066" + ], + "inability to coordinate movement when walk": [ + "HP:0002066" + ], + "inability to coordinate movements when walking": [ + "HP:0002066" + ], + "bradykinesia": [ + "HP:0002067" + ], + "slow movement": [ + "HP:0002067" + ], + "slow movements": [ + "HP:0002067" + ], + "slowness of movement": [ + "HP:0002067" + ], + "slowness of movements": [ + "HP:0002067" + ], + "neuromuscular dysphagia": [ + "HP:0002068" + ], + "bilateral tonic - clonic seizure": [ + "HP:0002069" + ], + "bilateral convulsive seizure": [ + "HP:0002069" + ], + "bilateral convulsive seizures": [ + "HP:0002069" + ], + "generalise convulsion": [ + "HP:0002069" + ], + "generalised convulsion": [ + "HP:0002069" + ], + "generalise tonic - clonic seizure ( without specification of onset )": [ + "HP:0002069" + ], + "generalised tonic - clonic seizure ( without specification of onset )": [ + "HP:0002069" + ], + "generalize convulsion": [ + "HP:0002069" + ], + "generalized convulsion": [ + "HP:0002069" + ], + "generalize tonic - clonic seizure ( without specification of onset )": [ + "HP:0002069" + ], + "generalized tonic - clonic seizure ( without specification of onset )": [ + "HP:0002069" + ], + "grand mal": [ + "HP:0002069" + ], + "grand mal seizure": [ + "HP:0002069" + ], + "grand mal seizures": [ + "HP:0002069" + ], + "seizure , tonic - clonic": [ + "HP:0002069" + ], + "seizures , tonic - clonic": [ + "HP:0002069" + ], + "tonic - clonic convulsion": [ + "HP:0002069" + ], + "tonic - clonic convulsions": [ + "HP:0002069" + ], + "limb ataxia": [ + "HP:0002070" + ], + "appendicular ataxia": [ + "HP:0002070" + ], + "abnormality of extrapyramidal motor function": [ + "HP:0002071" + ], + "extrapyramidal dysfunction": [ + "HP:0002071" + ], + "extrapyramidal sign": [ + "HP:0002071" + ], + "extrapyramidal signs": [ + "HP:0002071" + ], + "extrapyramidal symptom": [ + "HP:0002071" + ], + "extrapyramidal symptoms": [ + "HP:0002071" + ], + "extrapyramidal syndrome": [ + "HP:0002071" + ], + "extrapyramidal tract sign": [ + "HP:0002071" + ], + "extrapyramidal tract signs": [ + "HP:0002071" + ], + "chorea": [ + "HP:0002072" + ], + "choreatic disease": [ + "HP:0002072" + ], + "choreic movement": [ + "HP:0002072" + ], + "choreic movements": [ + "HP:0002072" + ], + "choreiform movement": [ + "HP:0002072" + ], + "choreiform movements": [ + "HP:0002072" + ], + "progressive cerebellar ataxia": [ + "HP:0002073" + ], + "cerebellar ataxia , progressive": [ + "HP:0002073" + ], + "progressive ataxia": [ + "HP:0002073" + ], + "increase neuronal autofluorescent lipopigment": [ + "HP:0002074" + ], + "increased neuronal autofluorescent lipopigment": [ + "HP:0002074" + ], + "neuronal lipopigments": [ + "HP:0002074" + ], + "dysdiadochokinesis": [ + "HP:0002075" + ], + "difficulty perform quick and alternate movement": [ + "HP:0002075" + ], + "difficulty performing quick and alternating movements": [ + "HP:0002075" + ], + "dysdiadochokinesia": [ + "HP:0002075" + ], + "migraine": [ + "HP:0002076" + ], + "intermittent migraine headache": [ + "HP:0002076" + ], + "intermittent migraine headaches": [ + "HP:0002076" + ], + "migraine headache": [ + "HP:0002076" + ], + "migraine headaches": [ + "HP:0002076" + ], + "migraine with aura": [ + "HP:0002077" + ], + "truncal ataxia": [ + "HP:0002078" + ], + "instability or lack of coordination of central trunk muscle": [ + "HP:0002078" + ], + "instability or lack of coordination of central trunk muscles": [ + "HP:0002078" + ], + "trunk ataxia": [ + "HP:0002078" + ], + "hypoplasia of the corpus callosum": [ + "HP:0002079" + ], + "corpus callosum hypoplasia": [ + "HP:0002079" + ], + "hypoplasia of corpus callosum": [ + "HP:0002079" + ], + "hypoplastic corpus callosum": [ + "HP:0002079" + ], + "underdevelopment of part of brain call corpus callosum": [ + "HP:0002079" + ], + "underdevelopment of part of brain called corpus callosum": [ + "HP:0002079" + ], + "intention tremor": [ + "HP:0002080" + ], + "cerebellar tremor": [ + "HP:0002080" + ], + "terminal tremor": [ + "HP:0002080" + ], + "migraine without aura": [ + "HP:0002083" + ], + "encephalocele": [ + "HP:0002084" + ], + "bifid skull": [ + "HP:0002084" + ], + "cranium bifidum": [ + "HP:0002084" + ], + "occipital encephalocele": [ + "HP:0002085" + ], + "brain tissue stick out through back of skull": [ + "HP:0002085" + ], + "brain tissue sticks out through back of skull": [ + "HP:0002085" + ], + "occipital meningoencephalocele": [ + "HP:0002085" + ], + "posterior encephalocele": [ + "HP:0002085" + ], + "abnormality of the respiratory system": [ + "HP:0002086" + ], + "respiratory abnormality": [ + "HP:0002086" + ], + "abnormality of the upper respiratory tract": [ + "HP:0002087" + ], + "upper respiratory tract issue": [ + "HP:0002087" + ], + "upper respiratory tract issues": [ + "HP:0002087" + ], + "abnormal lung morphology": [ + "HP:0002088" + ], + "abnormality of lung structure": [ + "HP:0002088" + ], + "abnormality of the lung": [ + "HP:0002088" + ], + "abnormality of the lungs": [ + "HP:0002088" + ], + "abnormally shape lung": [ + "HP:0002088" + ], + "abnormally shaped lung": [ + "HP:0002088" + ], + "lung disease": [ + "HP:0002088" + ], + "unusal lung shape": [ + "HP:0002088" + ], + "pulmonary hypoplasia": [ + "HP:0002089" + ], + "hypoplastic lung": [ + "HP:0002089" + ], + "hypoplastic lungs": [ + "HP:0002089" + ], + "lung hypoplasia": [ + "HP:0002089" + ], + "poorly develop lung": [ + "HP:0002089" + ], + "poorly developed lungs": [ + "HP:0002089" + ], + "small lung": [ + "HP:0002089" + ], + "underdeveloped lung": [ + "HP:0002089" + ], + "pneumonia": [ + "HP:0002090" + ], + "restrictive ventilatory defect": [ + "HP:0002091" + ], + "restrictive deficit on pulmonary function test": [ + "HP:0002091" + ], + "restrictive deficit on pulmonary function testing": [ + "HP:0002091" + ], + "restrictive deficit on pulmonary function tests": [ + "HP:0002091" + ], + "restrictive lung disease": [ + "HP:0002091" + ], + "restrictive respiratory disease": [ + "HP:0002091" + ], + "restrictive respiratory insufficiency": [ + "HP:0002091" + ], + "restrictive respiratory syndrome": [ + "HP:0002091" + ], + "spirometric restriction": [ + "HP:0002091" + ], + "stiff lung or chest wall causing decrease lung volume": [ + "HP:0002091" + ], + "stiff lung or chest wall causing decreased lung volume": [ + "HP:0002091" + ], + "pulmonary arterial hypertension": [ + "HP:0002092" + ], + "increase blood pressure in blood vessel of lung": [ + "HP:0002092" + ], + "increased blood pressure in blood vessels of lungs": [ + "HP:0002092" + ], + "primary pulmonary hypertension": [ + "HP:0002092" + ], + "pulmonary artery hypertension": [ + "HP:0002092" + ], + "respiratory insufficiency": [ + "HP:0002093" + ], + "progressive respiratory failure": [ + "HP:0002093" + ], + "respiratory function loss": [ + "HP:0002093" + ], + "respiratory impairment": [ + "HP:0002093" + ], + "dyspnea": [ + "HP:0002094" + ], + "abnormal breathing": [ + "HP:0002094" + ], + "breathe difficulty": [ + "HP:0002094", + "HP:0002098" + ], + "breathing difficulty": [ + "HP:0002094" + ], + "difficult to breathe": [ + "HP:0002094" + ], + "difficulty breathe": [ + "HP:0002094" + ], + "difficulty breathing": [ + "HP:0002094" + ], + "dyspnoea": [ + "HP:0002094" + ], + "pant": [ + "HP:0002094" + ], + "panting": [ + "HP:0002094" + ], + "shortness of breath": [ + "HP:0002094" + ], + "trouble breathe": [ + "HP:0002094" + ], + "trouble breathing": [ + "HP:0002094" + ], + "emphysema": [ + "HP:0002097" + ], + "pulmonary emphysema": [ + "HP:0002097" + ], + "respiratory distress": [ + "HP:0002098" + ], + "breathing difficulties": [ + "HP:0002098" + ], + "labor breathing": [ + "HP:0002098" + ], + "labored breathing": [ + "HP:0002098" + ], + "respiratory difficulty": [ + "HP:0002098" + ], + "respiratory difficulties": [ + "HP:0002098" + ], + "asthma": [ + "HP:0002099" + ], + "bronchial asthma": [ + "HP:0002099" + ], + "reactive airway disease": [ + "HP:0002099" + ], + "recurrent aspiration pneumonia": [ + "HP:0002100" + ], + "recurrent pneumonia due to aspiration ,": [ + "HP:0002100" + ], + "abnormal lung lobation": [ + "HP:0002101" + ], + "defective lung lobation": [ + "HP:0002101" + ], + "lung segmentation defect": [ + "HP:0002101" + ], + "lung segmentation defects": [ + "HP:0002101" + ], + "pleuritis": [ + "HP:0002102" + ], + "inflammation of tissue line lung and chest": [ + "HP:0002102" + ], + "inflammation of tissues lining lungs and chest": [ + "HP:0002102" + ], + "pleurisy": [ + "HP:0002102" + ], + "abnormal pleura morphology": [ + "HP:0002103" + ], + "abnormality of the pleura": [ + "HP:0002103" + ], + "apnea": [ + "HP:0002104" + ], + "absence of spontaneous respiration": [ + "HP:0002104" + ], + "apneic episode": [ + "HP:0002104" + ], + "apneic episodes": [ + "HP:0002104" + ], + "apnoea": [ + "HP:0002104" + ], + "hemoptysis": [ + "HP:0002105" + ], + "cough up blood": [ + "HP:0002105" + ], + "coughing up blood": [ + "HP:0002105" + ], + "cough up blood or blood - stain mucus": [ + "HP:0002105" + ], + "coughing up blood or blood - stained mucus": [ + "HP:0002105" + ], + "haemoptysis": [ + "HP:0002105" + ], + "pneumothorax": [ + "HP:0002107" + ], + "collapse lung": [ + "HP:0002107" + ], + "collapsed lung": [ + "HP:0002107" + ], + "spontaneous pneumothorax": [ + "HP:0002108" + ], + "spontaneous collapse lung": [ + "HP:0002108" + ], + "spontaneous collapsed lung": [ + "HP:0002108" + ], + "obsolete abnormality of the bronchus": [ + "HP:0002109" + ], + "obsolete abnormality of the bronchi": [ + "HP:0002109" + ], + "bronchiectasis": [ + "HP:0002110" + ], + "permanent enlargement of the airway of the lung": [ + "HP:0002110" + ], + "permanent enlargement of the airways of the lungs": [ + "HP:0002110" + ], + "obsolete restrictive deficit on pulmonary function test": [ + "HP:0002111" + ], + "obsolete restrictive deficit on pulmonary function testing": [ + "HP:0002111" + ], + "pulmonary infiltrates": [ + "HP:0002113" + ], + "lung infiltrates": [ + "HP:0002113" + ], + "pulmonic infiltration": [ + "HP:0002113" + ], + "abnormal cerebral ventricle morphology": [ + "HP:0002118" + ], + "abnormality of the cerebral ventricle": [ + "HP:0002118" + ], + "abnormality of the cerebral ventricles": [ + "HP:0002118" + ], + "ventriculomegaly": [ + "HP:0002119" + ], + "cerebral ventricular dilatation": [ + "HP:0002119" + ], + "dilate cerebral ventricle": [ + "HP:0002119" + ], + "dilated cerebral ventricle": [ + "HP:0002119" + ], + "dilated cerebral ventricles": [ + "HP:0002119" + ], + "dilate ventricle": [ + "HP:0002119" + ], + "dilated ventricles": [ + "HP:0002119" + ], + "enlarged cerebral ventricle": [ + "HP:0002119" + ], + "enlarged cerebral ventricles": [ + "HP:0002119" + ], + "enlarge ventricle": [ + "HP:0002119" + ], + "enlarged ventricles": [ + "HP:0002119" + ], + "enlarge ventricular system": [ + "HP:0002119" + ], + "enlarged ventricular system": [ + "HP:0002119" + ], + "large cerebral ventricle and cisterna": [ + "HP:0002119" + ], + "large cerebral ventricles and cisternae": [ + "HP:0002119" + ], + "ventricular dilatation": [ + "HP:0002119" + ], + "cerebral cortical atrophy": [ + "HP:0002120" + ], + "cerebral cortex atrophy": [ + "HP:0002120" + ], + "cortical atrophy": [ + "HP:0002120" + ], + "decrease in size of the outer layer of the brain due to loss of brain cell": [ + "HP:0002120" + ], + "decrease in size of the outer layer of the brain due to loss of brain cells": [ + "HP:0002120" + ], + "generalize non - motor ( absence ) seizure": [ + "HP:0002121" + ], + "generalized non - motor ( absence ) seizure": [ + "HP:0002121" + ], + "absence seizure": [ + "HP:0002121" + ], + "absence seizures": [ + "HP:0002121" + ], + "brief seizure with star spell": [ + "HP:0002121" + ], + "brief seizures with staring spells": [ + "HP:0002121" + ], + "generalise non - motor ( absence ) seizure": [ + "HP:0002121" + ], + "generalised non - motor ( absence ) seizure": [ + "HP:0002121" + ], + "generalise non - motor seizure": [ + "HP:0002121" + ], + "generalised non - motor seizure": [ + "HP:0002121" + ], + "petit mal": [ + "HP:0002121" + ], + "petit mal seizure": [ + "HP:0002121" + ], + "petit mal seizures": [ + "HP:0002121" + ], + "generalize myoclonic seizure": [ + "HP:0002123" + ], + "generalized myoclonic seizure": [ + "HP:0002123" + ], + "generalise epileptic myoclonus": [ + "HP:0002123" + ], + "generalised epileptic myoclonus": [ + "HP:0002123" + ], + "generalise myoclonic seizure": [ + "HP:0002123" + ], + "generalised myoclonic seizure": [ + "HP:0002123" + ], + "generalised myoclonic seizures": [ + "HP:0002123" + ], + "generalize epileptic myoclonus": [ + "HP:0002123" + ], + "generalized epileptic myoclonus": [ + "HP:0002123" + ], + "generalized myoclonic seizures": [ + "HP:0002123" + ], + "myoclonic epilepsy , progressive": [ + "HP:0002123" + ], + "myoclonus seizure": [ + "HP:0002123" + ], + "myoclonus seizures": [ + "HP:0002123" + ], + "polymicrogyria": [ + "HP:0002126" + ], + "more groove in brain": [ + "HP:0002126" + ], + "more grooves in brain": [ + "HP:0002126" + ], + "abnormal upper motor neuron morphology": [ + "HP:0002127" + ], + "abnormal shape of upper motor neuron": [ + "HP:0002127" + ], + "episodic ataxia": [ + "HP:0002131" + ], + "intermittent cerebellar ataxia": [ + "HP:0002131" + ], + "paroxysmal ataxia": [ + "HP:0002131" + ], + "porencephalic cyst": [ + "HP:0002132" + ], + "cavity within brain": [ + "HP:0002132" + ], + "status epilepticus": [ + "HP:0002133" + ], + "prolonged seizure": [ + "HP:0002133" + ], + "repeat seizure without recovery": [ + "HP:0002133" + ], + "repeated seizure without recovery": [ + "HP:0002133" + ], + "repeat seizure without recovery between them": [ + "HP:0002133" + ], + "repeated seizures without recovery between them": [ + "HP:0002133" + ], + "abnormality of the basal ganglion": [ + "HP:0002134" + ], + "abnormality of the basal ganglia": [ + "HP:0002134" + ], + "anomaly of the basal ganglion": [ + "HP:0002134" + ], + "anomaly of the basal ganglia": [ + "HP:0002134" + ], + "basal ganglion disease": [ + "HP:0002134" + ], + "basal ganglia disease": [ + "HP:0002134" + ], + "basal ganglion calcification": [ + "HP:0002135" + ], + "basal ganglia calcification": [ + "HP:0002135" + ], + "basal ganglia calcifications": [ + "HP:0002135" + ], + "calcification of the basal ganglion": [ + "HP:0002135" + ], + "calcification of the basal ganglia": [ + "HP:0002135" + ], + "broad - base gait": [ + "HP:0002136" + ], + "broad - based gait": [ + "HP:0002136" + ], + "broad base gait": [ + "HP:0002136" + ], + "broad based gait": [ + "HP:0002136" + ], + "wide base gait": [ + "HP:0002136" + ], + "wide based gait": [ + "HP:0002136" + ], + "wide base walk": [ + "HP:0002136" + ], + "wide based walk": [ + "HP:0002136" + ], + "wide - base gait": [ + "HP:0002136" + ], + "wide - based gait": [ + "HP:0002136" + ], + "subarachnoid hemorrhage": [ + "HP:0002138" + ], + "subarachnoid haemorrhage": [ + "HP:0002138" + ], + "arrhinencephaly": [ + "HP:0002139" + ], + "ischemic stroke": [ + "HP:0002140" + ], + "ischaemic stroke": [ + "HP:0002140" + ], + "gait imbalance": [ + "HP:0002141" + ], + "abnormality of balance": [ + "HP:0002141" + ], + "abnormality of equilibrium": [ + "HP:0002141" + ], + "imbalanced walk": [ + "HP:0002141" + ], + "abnormality of the spinal cord": [ + "HP:0002143" + ], + "spinal cord disease": [ + "HP:0002143" + ], + "spinal cord pathology": [ + "HP:0002143" + ], + "tether cord": [ + "HP:0002144" + ], + "tethered cord": [ + "HP:0002144" + ], + "occult spinal dysraphism": [ + "HP:0002144" + ], + "frontotemporal dementia": [ + "HP:0002145" + ], + "hypophosphatemia": [ + "HP:0002148" + ], + "hypophosphataemia": [ + "HP:0002148" + ], + "low blood phosphate level": [ + "HP:0002148" + ], + "hyperuricemia": [ + "HP:0002149" + ], + "high blood uric acid level": [ + "HP:0002149" + ], + "hyperuricaemia": [ + "HP:0002149" + ], + "hypercalciuria": [ + "HP:0002150" + ], + "elevate urine calcium level": [ + "HP:0002150" + ], + "elevated urine calcium levels": [ + "HP:0002150" + ], + "hypercalcinuria": [ + "HP:0002150" + ], + "increase serum lactate": [ + "HP:0002151" + ], + "increased serum lactate": [ + "HP:0002151" + ], + "high than normal level of lactate in blood": [ + "HP:0002151" + ], + "higher than normal levels of lactate in blood": [ + "HP:0002151" + ], + "increase blood lactate": [ + "HP:0002151" + ], + "increased blood lactate": [ + "HP:0002151" + ], + "hyperproteinemia": [ + "HP:0002152" + ], + "hyperkalemia": [ + "HP:0002153" + ], + "elevate serum potassium level": [ + "HP:0002153" + ], + "elevated serum potassium levels": [ + "HP:0002153" + ], + "hyperglycinemia": [ + "HP:0002154" + ], + "elevate blood glycine level": [ + "HP:0002154" + ], + "elevated blood glycine levels": [ + "HP:0002154" + ], + "hyperglycinaemia": [ + "HP:0002154" + ], + "hypertriglyceridemia": [ + "HP:0002155" + ], + "increase circulate tg level": [ + "HP:0002155" + ], + "increased circulating tg levels": [ + "HP:0002155" + ], + "increase plasma tg level": [ + "HP:0002155" + ], + "increased plasma tg levels": [ + "HP:0002155" + ], + "increase plasma triglyceride": [ + "HP:0002155" + ], + "increased plasma triglycerides": [ + "HP:0002155" + ], + "increase serum triglyceride": [ + "HP:0002155" + ], + "increased serum triglycerides": [ + "HP:0002155" + ], + "increase triglyceride": [ + "HP:0002155" + ], + "increased triglycerides": [ + "HP:0002155" + ], + "homocystinuria": [ + "HP:0002156" + ], + "high urine homocystine level": [ + "HP:0002156" + ], + "high urine homocystine levels": [ + "HP:0002156" + ], + "azotemia": [ + "HP:0002157" + ], + "azotaemia": [ + "HP:0002157" + ], + "heparan sulfate excretion in urine": [ + "HP:0002159" + ], + "heparan sulphate excretion in urine": [ + "HP:0002159" + ], + "hyperhomocystinemia": [ + "HP:0002160" + ], + "elevate blood homocystine": [ + "HP:0002160" + ], + "elevated blood homocystine": [ + "HP:0002160" + ], + "homocystinemia": [ + "HP:0002160" + ], + "hyperlysinemia": [ + "HP:0002161" + ], + "elevate blood lysine": [ + "HP:0002161" + ], + "elevated blood lysine": [ + "HP:0002161" + ], + "low posterior hairline": [ + "HP:0002162" + ], + "low hairline at back of neck": [ + "HP:0002162" + ], + "low posterior hair line": [ + "HP:0002162" + ], + "nail dysplasia": [ + "HP:0002164" + ], + "atypical nail growth": [ + "HP:0002164" + ], + "dysplastic nail": [ + "HP:0002164" + ], + "dysplastic nails": [ + "HP:0002164" + ], + "onychodysplasia": [ + "HP:0002164" + ], + "pterygium of nail": [ + "HP:0002165" + ], + "pterygium of nails": [ + "HP:0002165" + ], + "nail pterygium": [ + "HP:0002165" + ], + "impaired vibration sensation in the low limb": [ + "HP:0002166" + ], + "impaired vibration sensation in the lower limbs": [ + "HP:0002166" + ], + "decrease low limb vibratory sense": [ + "HP:0002166" + ], + "decreased lower limb vibratory sense": [ + "HP:0002166" + ], + "decreased vibratory sense in low limb": [ + "HP:0002166" + ], + "decreased vibratory sense in lower limbs": [ + "HP:0002166" + ], + "decreased vibratory sense in the low extremity": [ + "HP:0002166" + ], + "decreased vibratory sense in the lower extremities": [ + "HP:0002166" + ], + "decreased vibratory sense in the low limb": [ + "HP:0002166" + ], + "decreased vibratory sense in the lower limbs": [ + "HP:0002166" + ], + "diminished vibratory sensation in the leg": [ + "HP:0002166" + ], + "diminished vibratory sensation in the legs": [ + "HP:0002166" + ], + "distal sensory loss , especially vibratory sense": [ + "HP:0002166" + ], + "distal vibratory impairment of the low limb": [ + "HP:0002166" + ], + "distal vibratory impairment of the lower limbs": [ + "HP:0002166" + ], + "neurological speech impairment": [ + "HP:0002167" + ], + "speech disorder": [ + "HP:0002167" + ], + "speech impairment": [ + "HP:0002167" + ], + "speech impediment": [ + "HP:0002167" + ], + "scan speech": [ + "HP:0002168" + ], + "scanning speech": [ + "HP:0002168" + ], + "explosive speech": [ + "HP:0002168" + ], + "clonus": [ + "HP:0002169" + ], + "involuntary rhythmic muscular contraction and relaxation": [ + "HP:0002169" + ], + "involuntary rhythmic muscular contractions and relaxations": [ + "HP:0002169" + ], + "intracranial hemorrhage": [ + "HP:0002170" + ], + "bleed within the skull": [ + "HP:0002170" + ], + "bleeding within the skull": [ + "HP:0002170" + ], + "intracranial haemorrhage": [ + "HP:0002170" + ], + "gliosis": [ + "HP:0002171" + ], + "cerebral gliosis": [ + "HP:0002171" + ], + "excess astrocyte in brain": [ + "HP:0002171" + ], + "excess astrocytes in brain": [ + "HP:0002171" + ], + "postural instability": [ + "HP:0002172" + ], + "abnormal retropulsion test": [ + "HP:0002172" + ], + "balance impairment": [ + "HP:0002172" + ], + "imbalance": [ + "HP:0002172" + ], + "hypoglycemic seizure": [ + "HP:0002173" + ], + "hypoglycemic seizures": [ + "HP:0002173" + ], + "postural tremor": [ + "HP:0002174" + ], + "tremor , postural": [ + "HP:0002174" + ], + "spinal cord compression": [ + "HP:0002176" + ], + "pressure on spinal cord": [ + "HP:0002176" + ], + "opisthotonus": [ + "HP:0002179" + ], + "opisthotonos": [ + "HP:0002179" + ], + "neurodegeneration": [ + "HP:0002180" + ], + "neuro - degenerative disease": [ + "HP:0002180" + ], + "neurodegenerative disease": [ + "HP:0002180" + ], + "ongoing loss of nerve cell": [ + "HP:0002180" + ], + "ongoing loss of nerve cells": [ + "HP:0002180" + ], + "progressive neurodegenerative disorder": [ + "HP:0002180" + ], + "cerebral edema": [ + "HP:0002181" + ], + "brain edema": [ + "HP:0002181" + ], + "brain oedema": [ + "HP:0002181" + ], + "brain swelling": [ + "HP:0002181" + ], + "cerebral oedema": [ + "HP:0002181" + ], + "swell of brain": [ + "HP:0002181" + ], + "swelling of brain": [ + "HP:0002181" + ], + "phonophobia": [ + "HP:0002183" + ], + "fear of loud sound": [ + "HP:0002183" + ], + "fear of loud sounds": [ + "HP:0002183" + ], + "neurofibrillary tangle": [ + "HP:0002185" + ], + "neurofibrillary tangles": [ + "HP:0002185" + ], + "neurofibrillary tangle compose of disordered microtubule in neuron": [ + "HP:0002185" + ], + "neurofibrillary tangles composed of disordered microtubules in neurons": [ + "HP:0002185" + ], + "paired helical filament": [ + "HP:0002185" + ], + "paired helical filaments": [ + "HP:0002185" + ], + "apraxia": [ + "HP:0002186" + ], + "apraxias": [ + "HP:0002186" + ], + "intellectual disability , profound": [ + "HP:0002187" + ], + "iq less than 20": [ + "HP:0002187" + ], + "mental retardation , profound": [ + "HP:0002187" + ], + "profound mental retardation": [ + "HP:0002187" + ], + "delay cns myelination": [ + "HP:0002188" + ], + "delayed cns myelination": [ + "HP:0002188" + ], + "delay in central nervous system myelination": [ + "HP:0002188" + ], + "obsolete excessive daytime sleepiness": [ + "HP:0002189" + ], + "choroid plexus cyst": [ + "HP:0002190" + ], + "progressive spasticity": [ + "HP:0002191" + ], + "spasticity , progressive": [ + "HP:0002191" + ], + "pseudobulbar behavioral symptom": [ + "HP:0002193" + ], + "pseudobulbar behavioral symptoms": [ + "HP:0002193" + ], + "pseudobulbar behavioural symptom": [ + "HP:0002193" + ], + "pseudobulbar behavioural symptoms": [ + "HP:0002193" + ], + "delay gross motor development": [ + "HP:0002194" + ], + "delayed gross motor development": [ + "HP:0002194" + ], + "delay gross motor skill": [ + "HP:0002194" + ], + "delayed gross motor skills": [ + "HP:0002194" + ], + "delay motor skill": [ + "HP:0002194" + ], + "delayed motor skills": [ + "HP:0002194" + ], + "developmental delay , gross motor": [ + "HP:0002194" + ], + "gross motor delay": [ + "HP:0002194" + ], + "limited gross motor development": [ + "HP:0002194" + ], + "dysgenesis of the cerebellar vermis": [ + "HP:0002195" + ], + "myelopathy": [ + "HP:0002196" + ], + "generalize - onset seizure": [ + "HP:0002197" + ], + "generalized - onset seizure": [ + "HP:0002197" + ], + "generalise onset seizure": [ + "HP:0002197" + ], + "generalised onset seizure": [ + "HP:0002197" + ], + "generalise seizure": [ + "HP:0002197" + ], + "generalised seizures": [ + "HP:0002197" + ], + "generalise - onset seizure": [ + "HP:0002197" + ], + "generalised - onset seizure": [ + "HP:0002197" + ], + "generalize onset seizure": [ + "HP:0002197" + ], + "generalized onset seizure": [ + "HP:0002197" + ], + "generalize seizure": [ + "HP:0002197" + ], + "generalized seizures": [ + "HP:0002197" + ], + "generalized - onset seizures": [ + "HP:0002197" + ], + "primary generalise seizure": [ + "HP:0002197" + ], + "primary generalised seizure": [ + "HP:0002197" + ], + "primary generalize seizure": [ + "HP:0002197" + ], + "primary generalized seizure": [ + "HP:0002197" + ], + "dilate fourth ventricle": [ + "HP:0002198" + ], + "dilated fourth ventricle": [ + "HP:0002198" + ], + "enlarge fourth ventricle": [ + "HP:0002198" + ], + "enlarged fourth ventricle": [ + "HP:0002198" + ], + "hypocalcemic seizure": [ + "HP:0002199" + ], + "hypocalcemic seizures": [ + "HP:0002199" + ], + "low calcium seizure": [ + "HP:0002199" + ], + "low calcium seizures": [ + "HP:0002199" + ], + "seizure due to hypocalcemia": [ + "HP:0002199" + ], + "seizures due to hypocalcemia": [ + "HP:0002199" + ], + "pseudobulbar sign": [ + "HP:0002200" + ], + "pseudobulbar signs": [ + "HP:0002200" + ], + "pseudobulbar symptom": [ + "HP:0002200" + ], + "pseudobulbar symptoms": [ + "HP:0002200" + ], + "pleural effusion": [ + "HP:0002202" + ], + "fluid around lung": [ + "HP:0002202" + ], + "fluid around lungs": [ + "HP:0002202" + ], + "respiratory paralysis": [ + "HP:0002203" + ], + "pulmonary embolism": [ + "HP:0002204" + ], + "blood clot in artery of lung": [ + "HP:0002204" + ], + "recurrent respiratory infection": [ + "HP:0002205" + ], + "recurrent respiratory infections": [ + "HP:0002205" + ], + "frequent respiratory infection": [ + "HP:0002205" + ], + "frequent respiratory infections": [ + "HP:0002205" + ], + "multiple respiratory infection": [ + "HP:0002205" + ], + "multiple respiratory infections": [ + "HP:0002205" + ], + "respiratory infection , recurrent": [ + "HP:0002205" + ], + "respiratory infections , recurrent": [ + "HP:0002205" + ], + "susceptibility to respiratory infection": [ + "HP:0002205" + ], + "susceptibility to respiratory infections": [ + "HP:0002205" + ], + "pulmonary fibrosis": [ + "HP:0002206" + ], + "diffuse reticular or finely nodular infiltration": [ + "HP:0002207" + ], + "diffuse reticular or finely nodular infiltrations": [ + "HP:0002207" + ], + "coarse hair": [ + "HP:0002208" + ], + "coarse hair texture": [ + "HP:0002208" + ], + "rough hair texture": [ + "HP:0002208" + ], + "sparse scalp hair": [ + "HP:0002209" + ], + "decreased number of scalp follicle": [ + "HP:0002209" + ], + "decreased number of scalp follicles": [ + "HP:0002209" + ], + "hypotrichosis on scalp": [ + "HP:0002209" + ], + "reduce / lack of hair on scalp": [ + "HP:0002209" + ], + "reduced / lack of hair on scalp": [ + "HP:0002209" + ], + "reduction in the number of scalp follicle": [ + "HP:0002209" + ], + "reduction in the number of scalp follicles": [ + "HP:0002209" + ], + "scalp hair , thin": [ + "HP:0002209" + ], + "scalp hair , thinning": [ + "HP:0002209" + ], + "scalp hypotrichosis": [ + "HP:0002209" + ], + "sparse , thin scalp hair": [ + "HP:0002209" + ], + "sparse - absent scalp hair": [ + "HP:0002209" + ], + "thin scalp hair": [ + "HP:0002209" + ], + "white forelock": [ + "HP:0002211" + ], + "poliosis of anterior hair": [ + "HP:0002211" + ], + "poliosis of forelock hair": [ + "HP:0002211" + ], + "white part of hair above forehead": [ + "HP:0002211" + ], + "curly hair": [ + "HP:0002212" + ], + "fine hair": [ + "HP:0002213" + ], + "fine hair shaft": [ + "HP:0002213" + ], + "fine hair texture": [ + "HP:0002213" + ], + "thin hair": [ + "HP:0002213" + ], + "thin hair shaft": [ + "HP:0002213" + ], + "thin hair texture": [ + "HP:0002213" + ], + "thinned hair": [ + "HP:0002213" + ], + "sparse axillary hair": [ + "HP:0002215" + ], + "limited armpit hair": [ + "HP:0002215" + ], + "little underarm hair": [ + "HP:0002215" + ], + "sparse axillary and pubic hair": [ + "HP:0002215" + ], + "sparse scalp , axillary , and pubic hair": [ + "HP:0002215" + ], + "sparse to absent axillary hair": [ + "HP:0002215" + ], + "premature graying of hair": [ + "HP:0002216" + ], + "early graying": [ + "HP:0002216" + ], + "early greying": [ + "HP:0002216" + ], + "premature gray": [ + "HP:0002216" + ], + "premature graying": [ + "HP:0002216" + ], + "premature graying of the hair": [ + "HP:0002216" + ], + "premature grey": [ + "HP:0002216" + ], + "premature greying": [ + "HP:0002216" + ], + "premature greying of hair": [ + "HP:0002216" + ], + "premature greying of the hair": [ + "HP:0002216" + ], + "premature hair gray": [ + "HP:0002216" + ], + "premature hair graying": [ + "HP:0002216" + ], + "premature hair grey": [ + "HP:0002216" + ], + "premature hair greying": [ + "HP:0002216" + ], + "slow - grow hair": [ + "HP:0002217" + ], + "slow - growing hair": [ + "HP:0002217" + ], + "slow grow hair": [ + "HP:0002217" + ], + "slow growing hair": [ + "HP:0002217" + ], + "slow rate of hair growth": [ + "HP:0002217" + ], + "slow speed of hair growth": [ + "HP:0002217" + ], + "silver - gray hair": [ + "HP:0002218" + ], + "silver - gray hair color": [ + "HP:0002218" + ], + "silver - gray hair colour": [ + "HP:0002218" + ], + "silvery - gray hair": [ + "HP:0002218" + ], + "facial hypertrichosis": [ + "HP:0002219" + ], + "increase facial hair growth": [ + "HP:0002219" + ], + "increased facial hair growth": [ + "HP:0002219" + ], + "melanin pigment aggregation in hair shaft": [ + "HP:0002220" + ], + "melanin pigment aggregation in hair shafts": [ + "HP:0002220" + ], + "absent axillary hair": [ + "HP:0002221" + ], + "absent eyebrow": [ + "HP:0002223" + ], + "absent eyebrows": [ + "HP:0002223" + ], + "agenesis of eyebrow": [ + "HP:0002223", + "HP:0100840" + ], + "agenesis of eyebrows": [ + "HP:0002223" + ], + "aplasia of eyebrow": [ + "HP:0002223" + ], + "aplasia of eyebrows": [ + "HP:0002223" + ], + "failure of development of eyebrow": [ + "HP:0002223" + ], + "failure of development of eyebrows": [ + "HP:0002223" + ], + "loss of eyebrow": [ + "HP:0002223" + ], + "loss of eyebrows": [ + "HP:0002223" + ], + "miss eyebrow": [ + "HP:0002223", + "HP:0100840" + ], + "missing eyebrows": [ + "HP:0002223" + ], + "woolly hair": [ + "HP:0002224" + ], + "afro - textured hair": [ + "HP:0002224" + ], + "kink hair": [ + "HP:0002224" + ], + "kinked hair": [ + "HP:0002224" + ], + "kinky hair texture": [ + "HP:0002224" + ], + "nappy hair texture": [ + "HP:0002224" + ], + "wooly hair": [ + "HP:0002224" + ], + "sparse pubic hair": [ + "HP:0002225" + ], + "decrease sexual hair": [ + "HP:0002225" + ], + "decreased sexual hair": [ + "HP:0002225" + ], + "sparse to absent pubic hair": [ + "HP:0002225" + ], + "white eyebrow": [ + "HP:0002226" + ], + "blonde eyebrow": [ + "HP:0002226" + ], + "depigmented eyebrow": [ + "HP:0002226" + ], + "grey eyebrow": [ + "HP:0002226" + ], + "hypopigmented eyebrow": [ + "HP:0002226" + ], + "pale eyebrow": [ + "HP:0002226" + ], + "white eyelash": [ + "HP:0002227" + ], + "white eyelashes": [ + "HP:0002227" + ], + "blonde eyelash": [ + "HP:0002227" + ], + "blonde eyelashes": [ + "HP:0002227" + ], + "depigmented eyelash": [ + "HP:0002227" + ], + "depigmented eyelashes": [ + "HP:0002227" + ], + "grey eyelash": [ + "HP:0002227" + ], + "grey eyelashes": [ + "HP:0002227" + ], + "pale eyelash": [ + "HP:0002227" + ], + "pale eyelashes": [ + "HP:0002227" + ], + "obsolete alopecia areata": [ + "HP:0002229" + ], + "generalize hirsutism": [ + "HP:0002230" + ], + "generalized hirsutism": [ + "HP:0002230" + ], + "excessive hairiness over body": [ + "HP:0002230" + ], + "generalise hirsutism": [ + "HP:0002230" + ], + "generalised hirsutism": [ + "HP:0002230" + ], + "sparse body hair": [ + "HP:0002231" + ], + "limited body hair": [ + "HP:0002231" + ], + "little body hair": [ + "HP:0002231" + ], + "sparse to absent body hair": [ + "HP:0002231" + ], + "patchy alopecia": [ + "HP:0002232" + ], + "alopecia areata": [ + "HP:0002232" + ], + "patchy baldness": [ + "HP:0002232" + ], + "early balding": [ + "HP:0002234" + ], + "pili canaliculus": [ + "HP:0002235" + ], + "pili canaliculi": [ + "HP:0002235" + ], + "frontal upsweep of hair": [ + "HP:0002236" + ], + "cowlick": [ + "HP:0002236" + ], + "frontal cowlick": [ + "HP:0002236" + ], + "upswept frontal hair": [ + "HP:0002236" + ], + "upswept frontal hair pattern": [ + "HP:0002236" + ], + "upswept frontal hairline": [ + "HP:0002236" + ], + "gastrointestinal hemorrhage": [ + "HP:0002239" + ], + "gastrointestinal bleeding": [ + "HP:0002239" + ], + "gastrointestinal haemorrhage": [ + "HP:0002239" + ], + "gi haemorrhage": [ + "HP:0002239" + ], + "gi hemorrhage": [ + "HP:0002239" + ], + "hepatomegaly": [ + "HP:0002240" + ], + "enlarge liver": [ + "HP:0002240" + ], + "enlarged liver": [ + "HP:0002240" + ], + "abnormal intestine morphology": [ + "HP:0002242" + ], + "abnormality of the intestine": [ + "HP:0002242" + ], + "enteropathy": [ + "HP:0002242" + ], + "protein - losing enteropathy": [ + "HP:0002243" + ], + "abnormality of the small intestine": [ + "HP:0002244" + ], + "meckel diverticulum": [ + "HP:0002245" + ], + "abnormal duodenum morphology": [ + "HP:0002246" + ], + "abnormality of the duodenum": [ + "HP:0002246" + ], + "duodenal atresia": [ + "HP:0002247" + ], + "absence or narrowing of first part of small bowel": [ + "HP:0002247" + ], + "hematemesis": [ + "HP:0002248" + ], + "vomitting blood": [ + "HP:0002248" + ], + "melena": [ + "HP:0002249" + ], + "black faeces": [ + "HP:0002249" + ], + "black feces": [ + "HP:0002249" + ], + "abnormal large intestine morphology": [ + "HP:0002250" + ], + "abnormality of the large intestine": [ + "HP:0002250" + ], + "aganglionic megacolon": [ + "HP:0002251" + ], + "congenital megacolon": [ + "HP:0002251" + ], + "enlarge colon lack nerve cell": [ + "HP:0002251" + ], + "enlarged colon lacking nerve cells": [ + "HP:0002251" + ], + "hirschsprung disease": [ + "HP:0002251" + ], + "hirschsprung megacolon": [ + "HP:0002251" + ], + "megacolon": [ + "HP:0002251" + ], + "colonic diverticulum": [ + "HP:0002253" + ], + "colonic diverticula": [ + "HP:0002253" + ], + "colon diverticulum": [ + "HP:0002253" + ], + "colon diverticula": [ + "HP:0002253" + ], + "colonic diverticulosis": [ + "HP:0002253" + ], + "intermittent diarrhea": [ + "HP:0002254" + ], + "episodic diarrhea": [ + "HP:0002254" + ], + "episodic diarrhoea": [ + "HP:0002254" + ], + "intermittent diarrhoea": [ + "HP:0002254" + ], + "small bowel diverticulum": [ + "HP:0002256" + ], + "small bowel diverticula": [ + "HP:0002256" + ], + "chronic rhinitis": [ + "HP:0002257" + ], + "exaggerated cupid 's bow": [ + "HP:0002263" + ], + "cupid bow upper lip": [ + "HP:0002263" + ], + "cupid 's bow , accentuate": [ + "HP:0002263" + ], + "cupid 's bow , accentuated": [ + "HP:0002263" + ], + "cupid - bow shape upper lip": [ + "HP:0002263" + ], + "cupid - bow shaped upper lip": [ + "HP:0002263" + ], + "prominent cupid - bow of upper lip": [ + "HP:0002263" + ], + "large fleshy ear": [ + "HP:0002265" + ], + "large fleshy ears": [ + "HP:0002265" + ], + "focal clonic seizure": [ + "HP:0002266" + ], + "focal clonic seizures": [ + "HP:0002266" + ], + "localise clonic seizure": [ + "HP:0002266" + ], + "localised clonic seizure": [ + "HP:0002266" + ], + "localize clonic seizure": [ + "HP:0002266" + ], + "localized clonic seizure": [ + "HP:0002266" + ], + "partial clonic seizure": [ + "HP:0002266" + ], + "segmental clonic seizure": [ + "HP:0002266" + ], + "exaggerated startle response": [ + "HP:0002267" + ], + "exaggerated acoustic startle response": [ + "HP:0002267" + ], + "hyperekplexia": [ + "HP:0002267" + ], + "increase startle response": [ + "HP:0002267" + ], + "increased startle response": [ + "HP:0002267" + ], + "paroxysmal dystonia": [ + "HP:0002268" + ], + "episodic dystonia": [ + "HP:0002268" + ], + "abnormality of neuronal migration": [ + "HP:0002269" + ], + "abnormal neuronal migration": [ + "HP:0002269" + ], + "heterotopias / abnormal migration": [ + "HP:0002269" + ], + "migrational brain disorder": [ + "HP:0002269" + ], + "neuronal migration disorder": [ + "HP:0002269" + ], + "abnormality of the autonomic nervous system": [ + "HP:0002270" + ], + "obsolete autonomic dysregulation": [ + "HP:0002271" + ], + "tetraparesis": [ + "HP:0002273" + ], + "quadriparesis": [ + "HP:0002273" + ], + "poor motor coordination": [ + "HP:0002275" + ], + "horner syndrome": [ + "HP:0002277" + ], + "horner 's syndrome": [ + "HP:0002277" + ], + "oculosympathetic palsy": [ + "HP:0002277" + ], + "enlarge cisterna magna": [ + "HP:0002280" + ], + "enlarged cisterna magna": [ + "HP:0002280" + ], + "large cisterna magna": [ + "HP:0002280" + ], + "mega cisterna magna": [ + "HP:0002280" + ], + "obsolete gray matter heterotopias": [ + "HP:0002281" + ], + "gray matter heterotopia": [ + "HP:0002282" + ], + "gray matter heterotopias": [ + "HP:0002282" + ], + "grey matter heterotopia": [ + "HP:0002282" + ], + "grey matter heterotopias": [ + "HP:0002282" + ], + "heterotopia": [ + "HP:0002282" + ], + "heterotopias": [ + "HP:0002282" + ], + "neuronal heterotopia": [ + "HP:0002282" + ], + "global brain atrophy": [ + "HP:0002283" + ], + "diffuse brain atrophy": [ + "HP:0002283" + ], + "generalise brain atrophy": [ + "HP:0002283" + ], + "generalised brain atrophy": [ + "HP:0002283" + ], + "generalise brain degeneration": [ + "HP:0002283" + ], + "generalised brain degeneration": [ + "HP:0002283" + ], + "generalised cerebral atrophy": [ + "HP:0002283" + ], + "generalize brain atrophy": [ + "HP:0002283" + ], + "generalized brain atrophy": [ + "HP:0002283" + ], + "generalize brain degeneration": [ + "HP:0002283" + ], + "generalized brain degeneration": [ + "HP:0002283" + ], + "generalize cerebral atrophy": [ + "HP:0002283" + ], + "generalized cerebral atrophy": [ + "HP:0002283" + ], + "fair hair": [ + "HP:0002286" + ], + "blond hair": [ + "HP:0002286" + ], + "fair hair color": [ + "HP:0002286" + ], + "fair hair colour": [ + "HP:0002286" + ], + "flaxen hair color": [ + "HP:0002286" + ], + "flaxen hair colour": [ + "HP:0002286" + ], + "light color hair": [ + "HP:0002286" + ], + "light colored hair": [ + "HP:0002286" + ], + "light colour hair": [ + "HP:0002286" + ], + "light coloured hair": [ + "HP:0002286" + ], + "sandy hair color": [ + "HP:0002286" + ], + "sandy hair colour": [ + "HP:0002286" + ], + "straw color hair": [ + "HP:0002286" + ], + "straw colored hair": [ + "HP:0002286" + ], + "straw colour hair": [ + "HP:0002286" + ], + "straw coloured hair": [ + "HP:0002286" + ], + "towhead ( hair color )": [ + "HP:0002286" + ], + "progressive alopecia": [ + "HP:0002287" + ], + "alopecia universalis": [ + "HP:0002289" + ], + "alopecia , complete": [ + "HP:0002289" + ], + "universal alopecia": [ + "HP:0002289" + ], + "poliosis": [ + "HP:0002290" + ], + "patch of white hair": [ + "HP:0002290" + ], + "white patch": [ + "HP:0002290" + ], + "frontal balding": [ + "HP:0002292" + ], + "male pattern baldness": [ + "HP:0002292" + ], + "alopecia of scalp": [ + "HP:0002293" + ], + "absence of scalp hair": [ + "HP:0002293" + ], + "baldness": [ + "HP:0002293" + ], + "miss scalp hair": [ + "HP:0002293" + ], + "missing scalp hair": [ + "HP:0002293" + ], + "pathologic hair loss from scalp": [ + "HP:0002293" + ], + "scalp hair loss": [ + "HP:0002293" + ], + "progressive hypotrichosis": [ + "HP:0002296" + ], + "red hair": [ + "HP:0002297" + ], + "ginger hair color": [ + "HP:0002297" + ], + "ginger hair colour": [ + "HP:0002297" + ], + "red hair color": [ + "HP:0002297" + ], + "red hair colour": [ + "HP:0002297" + ], + "red head ( hair color )": [ + "HP:0002297" + ], + "absent hair": [ + "HP:0002298" + ], + "brittle hair": [ + "HP:0002299" + ], + "easily breakable hair": [ + "HP:0002299" + ], + "fracture hair": [ + "HP:0002299" + ], + "fractured hair": [ + "HP:0002299" + ], + "fragile hair": [ + "HP:0002299" + ], + "reduce tensile strength of hair": [ + "HP:0002299" + ], + "reduced tensile strength of hair": [ + "HP:0002299" + ], + "mutism": [ + "HP:0002300" + ], + "inability to speak": [ + "HP:0002300" + ], + "muteness": [ + "HP:0002300" + ], + "hemiplegia": [ + "HP:0002301" + ], + "paralysis on one side of body": [ + "HP:0002301" + ], + "akinesia": [ + "HP:0002304" + ], + "athetosis": [ + "HP:0002305" + ], + "athetoid movement": [ + "HP:0002305" + ], + "athetoid movements": [ + "HP:0002305" + ], + "involuntary writhing movement": [ + "HP:0002305" + ], + "involuntary writhing movements": [ + "HP:0002305" + ], + "involuntary writhe movement in finger , hand , toe , and foot": [ + "HP:0002305" + ], + "involuntary writhing movements in fingers , hands , toes , and feet": [ + "HP:0002305" + ], + "drool": [ + "HP:0002307" + ], + "drooling": [ + "HP:0002307" + ], + "dribble": [ + "HP:0002307" + ], + "dribbling": [ + "HP:0002307" + ], + "sialorrhea": [ + "HP:0002307" + ], + "arnold - chiari malformation": [ + "HP:0002308" + ], + "chiari malformation": [ + "HP:0002308" + ], + "orofacial dyskinesia": [ + "HP:0002310" + ], + "orofacial dyskinesias": [ + "HP:0002310" + ], + "incoordination": [ + "HP:0002311" + ], + "difficulty in coordination": [ + "HP:0002311" + ], + "difficulties in coordination": [ + "HP:0002311" + ], + "incoordination of limb movement": [ + "HP:0002311" + ], + "incoordination of limb movements": [ + "HP:0002311" + ], + "limb incoordination": [ + "HP:0002311" + ], + "clumsiness": [ + "HP:0002312" + ], + "spastic paraparesis": [ + "HP:0002313" + ], + "degeneration of the lateral corticospinal tract": [ + "HP:0002314" + ], + "degeneration of the lateral corticospinal tracts": [ + "HP:0002314" + ], + "degeneration of lateral corticospinal tract": [ + "HP:0002314" + ], + "degeneration of lateral corticospinal tracts": [ + "HP:0002314" + ], + "headache": [ + "HP:0002315" + ], + "headaches": [ + "HP:0002315" + ], + "unsteady gait": [ + "HP:0002317" + ], + "gait instability": [ + "HP:0002317" + ], + "unsteady walk": [ + "HP:0002317" + ], + "cervical myelopathy": [ + "HP:0002318" + ], + "vertigo": [ + "HP:0002321" + ], + "dizziness": [ + "HP:0002321" + ], + "dizzy spell": [ + "HP:0002321" + ], + "rest tremor": [ + "HP:0002322" + ], + "resting tremor": [ + "HP:0002322" + ], + "parkinsonian tremor": [ + "HP:0002322" + ], + "tremor at rest": [ + "HP:0002322" + ], + "anencephaly": [ + "HP:0002323" + ], + "embryonic anencephaly": [ + "HP:0002323" + ], + "fetal anencephaly": [ + "HP:0002323" + ], + "foetal anencephaly": [ + "HP:0002323" + ], + "hydranencephaly": [ + "HP:0002324" + ], + "hydrancephaly": [ + "HP:0002324" + ], + "transient ischemic attack": [ + "HP:0002326" + ], + "mini stroke": [ + "HP:0002326" + ], + "transient ischaemic attack": [ + "HP:0002326" + ], + "transient ischaemic attacks": [ + "HP:0002326" + ], + "transient ischemic attacks": [ + "HP:0002326" + ], + "drowsiness": [ + "HP:0002329" + ], + "sleepy": [ + "HP:0002329" + ], + "paroxysmal drowsiness": [ + "HP:0002330" + ], + "recurrent paroxysmal headache": [ + "HP:0002331" + ], + "lack of peer relationship": [ + "HP:0002332" + ], + "lack of peer relationships": [ + "HP:0002332" + ], + "motor deterioration": [ + "HP:0002333" + ], + "progressive degeneration of movement": [ + "HP:0002333" + ], + "abnormal cerebellar vermis morphology": [ + "HP:0002334" + ], + "abnormality of the cerebellar vermis": [ + "HP:0002334" + ], + "agenesis of cerebellar vermis": [ + "HP:0002335" + ], + "cerebellar vermis aplasia": [ + "HP:0002335" + ], + "vermian agenesis": [ + "HP:0002335" + ], + "abnormal caudate nucleus morphology": [ + "HP:0002339" + ], + "abnormality of the caudate nucleus": [ + "HP:0002339" + ], + "caudate atrophy": [ + "HP:0002340" + ], + "caudate degeneration": [ + "HP:0002340" + ], + "cervical cord compression": [ + "HP:0002341" + ], + "cervical cord compression myelopathy": [ + "HP:0002341" + ], + "intellectual disability , moderate": [ + "HP:0002342" + ], + "iq between 34 and 49": [ + "HP:0002342" + ], + "mental retardation , moderate": [ + "HP:0002342" + ], + "moderate mental deficiency": [ + "HP:0002342" + ], + "moderate mental retardation": [ + "HP:0002342" + ], + "normal pressure hydrocephalus": [ + "HP:0002343" + ], + "normal - pressure hydrocephalus": [ + "HP:0002343" + ], + "progressive neurologic deterioration": [ + "HP:0002344" + ], + "neurologic deterioration": [ + "HP:0002344" + ], + "neurologic deterioration , progressive": [ + "HP:0002344" + ], + "progressive mental deterioration": [ + "HP:0002344" + ], + "progressive neurodegeneration": [ + "HP:0002344" + ], + "worsen neurological symptom": [ + "HP:0002344" + ], + "worsening neurological symptoms": [ + "HP:0002344" + ], + "action tremor": [ + "HP:0002345" + ], + "ataxic tremor": [ + "HP:0002345" + ], + "head tremor": [ + "HP:0002346" + ], + "focal aware seizure": [ + "HP:0002349" + ], + "focal aware seizures": [ + "HP:0002349" + ], + "focal seizure with retained awareness": [ + "HP:0002349" + ], + "focal seizure without impairment of awareness": [ + "HP:0002349" + ], + "focal seizure without impairment of consciousness or awareness": [ + "HP:0002349" + ], + "focal seizures without impairment of consciousness or awareness": [ + "HP:0002349" + ], + "partial seizure with retained awareness": [ + "HP:0002349" + ], + "partial seizure without impairment of awareness": [ + "HP:0002349" + ], + "simple partial seizure": [ + "HP:0002349" + ], + "simple partial seizures": [ + "HP:0002349" + ], + "cerebellar cyst": [ + "HP:0002350" + ], + "cerebellar cysts": [ + "HP:0002350" + ], + "leukoencephalopathy": [ + "HP:0002352" + ], + "eeg abnormality": [ + "HP:0002353" + ], + "abnormal eeg": [ + "HP:0002353" + ], + "abnormal electroencephalogram": [ + "HP:0002353" + ], + "eeg abnormalities": [ + "HP:0002353" + ], + "electroencephalogram abnormal": [ + "HP:0002353" + ], + "electroencephalogram abnormality": [ + "HP:0002353" + ], + 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"persistent cavum septum pellucidum": [ + "HP:0002389" + ], + "widen cavum septum pellucidum": [ + "HP:0002389" + ], + "widened cavum septum pellucidum": [ + "HP:0002389" + ], + "spinal arteriovenous malformation": [ + "HP:0002390" + ], + "eeg with polyspike wave complex": [ + "HP:0002392" + ], + "eeg with polyspike wave complexes": [ + "HP:0002392" + ], + "eeg : spike and multispike wave , 3 - 4 hz": [ + "HP:0002392" + ], + "eeg : spike and multispike waves , 3 - 4 hz": [ + "HP:0002392" + ], + "low limb hyperreflexia": [ + "HP:0002395" + ], + "lower limb hyperreflexia": [ + "HP:0002395" + ], + "brisk low extremity reflex": [ + "HP:0002395" + ], + "brisk lower extremity reflexes": [ + "HP:0002395" + ], + "hyperreflexia in low limb": [ + "HP:0002395" + ], + "hyperreflexia in lower limbs": [ + "HP:0002395" + ], + "hyperreflexia in the low limb": [ + "HP:0002395" + ], + "hyperreflexia in the lower limbs": [ + "HP:0002395" + ], + "increase deep tendon reflex in the low limb": [ + 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sign": [ + "HP:0002423" + ], + "long - tract signs": [ + "HP:0002423" + ], + "long tract sign": [ + "HP:0002423" + ], + "long tract signs": [ + "HP:0002423" + ], + "anarthria": [ + "HP:0002425" + ], + "loss of articulate speech": [ + "HP:0002425" + ], + "expressive aphasia": [ + "HP:0002427" + ], + "broca 's aphasia": [ + "HP:0002427" + ], + "loss of expressive speech": [ + "HP:0002427" + ], + "motor aphasia": [ + "HP:0002427" + ], + "non - fluent aphasia": [ + "HP:0002427" + ], + "meningocele": [ + "HP:0002435" + ], + "occipital meningocele": [ + "HP:0002436" + ], + "cerebellar malformation": [ + "HP:0002438" + ], + "frontolimbic dementia": [ + "HP:0002439" + ], + "dyscalculia": [ + "HP:0002442" + ], + "difficulty make arithmetical calculation": [ + "HP:0002442" + ], + "difficulty making arithmetical calculations": [ + "HP:0002442" + ], + "hypothalamic hamartoma": [ + "HP:0002444" + ], + "tetraplegia": [ + "HP:0002445" + ], + "paralysis of all four limb": [ + "HP:0002445" + ], + "paralysis of all four limbs": [ + "HP:0002445" + ], + "quadriplegia": [ + "HP:0002445" + ], + "astrocytosis": [ + "HP:0002446" + ], + "increase in astrocyte number": [ + "HP:0002446" + ], + "progressive encephalopathy": [ + "HP:0002448" + ], + "progressive brain disease": [ + "HP:0002448" + ], + "abnormal motor neuron morphology": [ + "HP:0002450" + ], + "abnormal shape of motor neuron": [ + "HP:0002450" + ], + "limb dystonia": [ + "HP:0002451" + ], + "abnormal globus pallidus morphology": [ + "HP:0002453" + ], + "eye of the tiger anomaly of globus pallidus": [ + "HP:0002454" + ], + "abnormal head movement": [ + "HP:0002457" + ], + "abnormal head movements": [ + "HP:0002457" + ], + "obsolete dysautonomia": [ + "HP:0002459" + ], + "distal muscle weakness": [ + "HP:0002460" + ], + "distal limb muscle weakness": [ + "HP:0002460" + ], + "distal limb muscle weakness due to peripheral neuropathy": [ + "HP:0002460" + ], + "distal limb weakness": [ + "HP:0002460" + ], + "distal muscular weakness": [ + "HP:0002460" + ], + "distal paresis": [ + "HP:0002460" + ], + "muscle weakness , distal": [ + "HP:0002460" + ], + "muscle weakness , distal limb , due to neuronopathy": [ + "HP:0002460" + ], + "muscle weakness , distal limbs , due to neuronopathy": [ + "HP:0002460" + ], + "weakness of distal muscle": [ + "HP:0002460" + ], + "weakness of distal muscles": [ + "HP:0002460" + ], + "weakness of outermost muscle": [ + "HP:0002460" + ], + "weakness of outermost muscles": [ + "HP:0002460" + ], + "dense calcification in the cerebellar dentate nucleus": [ + "HP:0002461" + ], + "dense calcifications in the cerebellar dentate nucleus": [ + "HP:0002461" + ], + "language impairment": [ + "HP:0002463" + ], + "language disorder": [ + "HP:0002463" + ], + "spastic dysarthria": [ + "HP:0002464" + ], + "rigid dysarthria": [ + "HP:0002464" + ], + "poor speech": [ + "HP:0002465" + ], + "difficulty speaking": [ + "HP:0002465" + ], + "problem speak": [ + "HP:0002465" + ], + "problems speaking": 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relaxation of muscle fibers after contraction": [ + "HP:0002486" + ], + "delay relaxation of muscle fibre after contraction": [ + "HP:0002486" + ], + "delayed relaxation of muscle fibres after contraction": [ + "HP:0002486" + ], + "hyperkinetic movement": [ + "HP:0002487" + ], + "hyperkinetic movements": [ + "HP:0002487" + ], + "hyperkinesia": [ + "HP:0002487" + ], + "hyperkinesis": [ + "HP:0002487" + ], + "muscle spasm": [ + "HP:0003394" + ], + "muscle spasms": [ + "HP:0002487" + ], + "acute leukemia": [ + "HP:0002488" + ], + "acute blood cancer": [ + "HP:0002488" + ], + "acute leukaemia": [ + "HP:0002488" + ], + "acute leukemias": [ + "HP:0002488" + ], + "increase csf lactate": [ + "HP:0002490" + ], + "increased csf lactate": [ + "HP:0002490" + ], + "hyperlactatorachia": [ + "HP:0002490" + ], + "increase cerebrospinal fluid lactate": [ + "HP:0002490" + ], + "increased cerebrospinal fluid lactate": [ + "HP:0002490" + ], + "increase csf lactic acid": [ + "HP:0002490" + ], + "increased csf lactic acid": [ + "HP:0002490" + ], + "spasticity of facial muscle": [ + "HP:0002491" + ], + "spasticity of facial muscles": [ + "HP:0002491" + ], + "increased stiffness of facial muscle": [ + "HP:0002491" + ], + "increased stiffness of facial muscles": [ + "HP:0002491" + ], + "increase tone of facial muscle": [ + "HP:0002491" + ], + "increased tone of facial muscles": [ + "HP:0002491" + ], + "spasticity of the facial muscle": [ + "HP:0002491" + ], + "spasticity of the facial muscles": [ + "HP:0002491" + ], + "morphological abnormality of the corticospinal tract": [ + "HP:0002492" + ], + "abnormality of the corticospinal tract": [ + "HP:0002492" + ], + "involvement of the corticospinal pathway": [ + "HP:0002492" + ], + "involvement of the corticospinal pathways": [ + "HP:0002492" + ], + "upper motor neuron dysfunction": [ + "HP:0002493" + ], + "corticospinal tract dysfunction": [ + "HP:0002493" + ], + "pyramidal tract dysfunction": [ + "HP:0002493" + ], + "abnormal rapid eye movement sleep": [ + "HP:0002494" + ], + "abnormal rem sleep": [ + "HP:0002494" + ], + "impaired vibratory sensation": [ + "HP:0002495" + ], + "decrease vibration sense": [ + "HP:0002495" + ], + "decreased vibration sense": [ + "HP:0002495" + ], + "decreased vibratory sense": [ + "HP:0002495" + ], + "diminished vibratory sense": [ + "HP:0002495" + ], + "hypopallesthesia": [ + "HP:0002495" + ], + "impaired vibratory sense": [ + "HP:0002495" + ], + "spastic ataxia": [ + "HP:0002497" + ], + "abnormal cerebral white matter morphology": [ + "HP:0002500" + ], + "abnormality of subcortical white matter": [ + "HP:0002500" + ], + "abnormality of the cerebral white matter": [ + "HP:0002500" + ], + "cerebral white matter abnormality": [ + "HP:0002500" + ], + "cerebral white matter abnormalities": [ + "HP:0002500" + ], + "cortical white matter abnormality see on mri": [ + "HP:0002500" + ], + "cortical white matter abnormalities seen on mri": [ + "HP:0002500" + ], + "leukoaraiosis": [ + "HP:0002500" + ], + "white matter abnormality": [ + "HP:0002500" + ], + "white matter abnormalities": [ + "HP:0002500" + ], + "white matter alteration": [ + "HP:0002500" + ], + "white matter alterations": [ + "HP:0002500" + ], + "spasticity of pharyngeal muscle": [ + "HP:0002501" + ], + "spasticity of pharyngeal muscles": [ + "HP:0002501" + ], + "spinocerebellar tract degeneration": [ + "HP:0002503" + ], + "degeneration of the spinocerebellar tract": [ + "HP:0002503" + ], + "degeneration of the spinocerebellar tracts": [ + "HP:0002503" + ], + "spinocerebellar degeneration": [ + "HP:0002503" + ], + "calcification of the small brain vessel": [ + "HP:0002504" + ], + "calcification of the small brain vessels": [ + "HP:0002504" + ], + "progressive inability to walk": [ + "HP:0002505" + ], + "diffuse cerebral atrophy": [ + "HP:0002506" + ], + "cerebral atrophy , diffuse": [ + "HP:0002506" + ], + "semilobar holoprosencephaly": [ + "HP:0002507" + ], + "brainstem dysplasia": [ + "HP:0002508" + ], + "brainstem hypoplasia / dysplasia": [ + "HP:0002508" + ], + "malformation of brainstem structure": [ + "HP:0002508" + ], + "malformation of brainstem structures": [ + "HP:0002508" + ], + "limb hypertonia": [ + "HP:0002509" + ], + "increased muscle tone of arm or leg": [ + "HP:0002509" + ], + "spastic tetraplegia": [ + "HP:0002510" + ], + "spastic quadriplegia": [ + "HP:0002510" + ], + "alzheimer disease": [ + "HP:0002511" + ], + "late - onset form of familial alzheimer disease": [ + "HP:0002511" + ], + "brain stem compression": [ + "HP:0002512" + ], + "cerebral calcification": [ + "HP:0002514" + ], + "abnormal deposit of calcium in the brain": [ + "HP:0002514" + ], + "abnormal deposits of calcium in the brain": [ + "HP:0002514" + ], + "brain calcification": [ + "HP:0002514" + ], + "intracerebral calcification": [ + "HP:0002514" + ], + "intracerebral calcifications": [ + "HP:0002514" + ], + "intracranial calcification": [ + "HP:0002514" + ], + "intracranial calcifications": [ + "HP:0002514" + ], + "waddle gait": [ + "HP:0002515" + ], + "waddling gait": [ + "HP:0002515" + ], + "'waddling ' gait": [ + "HP:0002515" + ], + "waddle walk": [ + "HP:0002515" + ], + "waddling walk": [ + "HP:0002515" + ], + "increase intracranial pressure": [ + "HP:0002516" + ], + "increased intracranial pressure": [ + "HP:0002516" + ], + "intracranial hypertension": [ + "HP:0002516" + ], + "intracranial pressure elevation": [ + "HP:0002516" + ], + "rise in pressure inside skull": [ + "HP:0002516" + ], + "abnormal periventricular white matter morphology": [ + "HP:0002518" + ], + "abnormality of the periventricular white matter": [ + "HP:0002518" + ], + "periventricular white matter abnormality": [ + "HP:0002518" + ], + "periventricular white matter abnormalities": [ + "HP:0002518" + ], + "hypnagogic hallucination": [ + "HP:0002519" + ], + "hypnagogic hallucinations": [ + "HP:0002519" + ], + "hypsarrhythmia": [ + "HP:0002521" + ], + "hypsarrhythmia by eeg": [ + "HP:0002521" + ], + "areflexia of low limb": [ + "HP:0002522" + ], + "areflexia of lower limbs": [ + "HP:0002522" + ], + "absent low limb tendon reflex": [ + "HP:0002522" + ], + "absent lower limb tendon reflexes": [ + "HP:0002522" + ], + "areflexia in low limb": [ + "HP:0002522" + ], + "areflexia in lower limbs": [ + "HP:0002522" + ], + "areflexia of the low limb": [ + "HP:0002522" + ], + "areflexia of the lower limbs": [ + "HP:0002522" + ], + "areflexia , low limb": [ + "HP:0002522" + ], + "areflexia , lower limbs": [ + "HP:0002522" + ], + "cataplexy": [ + "HP:0002524" + ], + "deficit in nonword repetition": [ + "HP:0002526" + ], + "fall": [ + "HP:0002527" + ], + "falls": [ + "HP:0002527" + ], + "granulovacuolar degeneration": [ + "HP:0002528" + ], + "neuronal loss in central nervous system": [ + "HP:0002529" + ], + "loss of brain cell": [ + "HP:0002529" + ], + "loss of brain cells": [ + "HP:0002529" + ], + "neuronal loss": [ + "HP:0002529" + ], + "neuronal loss in cns": [ + "HP:0002529" + ], + "axial dystonia": [ + "HP:0002530" + ], + "truncal dystonia": [ + "HP:0002530" + ], + "abnormal posturing": [ + "HP:0002533" + ], + "abnormal cortical gyration": [ + "HP:0002536" + ], + "abnormal gyration": [ + "HP:0002536" + ], + "cerebral gyral anomaly": [ + "HP:0002536" + ], + "cerebral gyral anomalies": [ + "HP:0002536" + ], + "abnormal cerebral cortex morphology": [ + "HP:0002538" + ], + "abnormality of the cerebral cortex": [ + "HP:0002538" + ], + "cortical dysplasia": [ + "HP:0002539" + ], + "neocortical dysplasia": [ + "HP:0002539" + ], + "inability to walk": [ + "HP:0002540" + ], + "non - ambulatory": [ + "HP:0002540" + ], + "olivopontocerebellar atrophy": [ + "HP:0002542" + ], + "olivopontocerebellar degeneration": [ + "HP:0002542" + ], + "retrocollis": [ + "HP:0002544" + ], + "patchy demyelination of subcortical white matter": [ + "HP:0002545" + ], + "incomprehensible speech": [ + "HP:0002546" + ], + "parkinsonism with favorable response to dopaminergic medication": [ + "HP:0002548" + ], + "favorable response to levodopa": [ + "HP:0002548" + ], + "favourable response to levodopa": [ + "HP:0002548" + ], + "parkinsonism with favourable response to dopaminergic medication": [ + "HP:0002548" + ], + "deficit in phonologic short - term memory": [ + "HP:0002549" + ], + "deficit in non - word repetition": [ + "HP:0002549" + ], + "impaired non - word repetition": [ + "HP:0002549" + ], + "absent facial hair": [ + "HP:0002550" + ], + "trichodysplasia": [ + "HP:0002552" + ], + "generalise trichodysplasia": [ + "HP:0002552" + ], + "generalised trichodysplasia": [ + "HP:0002552" + ], + "generalize trichodysplasia": [ + "HP:0002552" + ], + "generalized trichodysplasia": [ + "HP:0002552" + ], + "highly arch eyebrow": [ + "HP:0002553" + ], + "highly arched eyebrow": [ + "HP:0002553" + ], + "arch eyebrow": [ + "HP:0002553" + ], + "arched eyebrows": [ + "HP:0002553" + ], + "bow and upward slanting eyebrow": [ + "HP:0002553" + ], + "bowed and upward slanting eyebrows": [ + "HP:0002553" + ], + "broad , arch eyebrow": [ + "HP:0002553" + ], + "broad , arched eyebrows": [ + "HP:0002553" + ], + "high arch eyebrow": [ + "HP:0002553" + ], + "high arched eyebrows": [ + "HP:0002553" + ], + "high , round eyebrow": [ + "HP:0002553" + ], + "high , rounded eyebrows": [ + "HP:0002553" + ], + "high - arch eyebrow": [ + "HP:0002553" + ], + "high - arched eyebrows": [ + "HP:0002553" + ], + "thick , flare eyebrow": [ + "HP:0002553" + ], + "thick , flared eyebrows": [ + "HP:0002553" + ], + "absent pubic hair": [ + "HP:0002555" + ], + "hypoplastic nipple": [ + "HP:0002557" + ], + "hypoplastic nipples": [ + "HP:0002557" + ], + "nipple hypoplasia": [ + "HP:0002557" + ], + "small nipple": [ + "HP:0002557" + ], + "small nipples": [ + "HP:0002557" + ], + "supernumerary nipple": [ + "HP:0002558" + ], + "accessory mamilla": [ + "HP:0002558" + ], + "accessory mamillas": [ + "HP:0002558" + ], + "accessory nipple": [ + "HP:0002558" + ], + "accessory nipples": [ + "HP:0002558" + ], + "increase nipple number": [ + "HP:0002558" + ], + "increased nipple number": [ + "HP:0002558" + ], + "supernumerary nipples": [ + "HP:0002558" + ], + "absent nipple": [ + "HP:0002561" + ], + "absent nipples": [ + "HP:0002561" + ], + "athelia": [ + "HP:0002561" + ], + "low - set nipple": [ + "HP:0002562" + ], + "low - set nipples": [ + "HP:0002562" + ], + "constrictive pericarditis": [ + "HP:0002563" + ], + "obsolete malformation of the heart and great vessel": [ + "HP:0002564" + ], + "obsolete malformation of the heart and great vessels": [ + "HP:0002564" + ], + "intestinal malrotation": [ + "HP:0002566" + ], + "gut malrotation": [ + "HP:0002566" + ], + "malrotation": [ + "HP:0002566" + ], + "steatorrhea": [ + "HP:0002570" + ], + "fat in faeces": [ + "HP:0002570" + ], + "fat in feces": [ + "HP:0002570" + ], + "fatty stool": [ + "HP:0002570" + ], + "achalasia": [ + "HP:0002571" + ], + "achalasia of the esophagus": [ + "HP:0002571" + ], + "achalasia of the oesophagus": [ + "HP:0002571" + ], + "episodic vomit": [ + "HP:0002572" + ], + "episodic vomiting": [ + "HP:0002572" + ], + "frequent vomit": [ + "HP:0002572" + ], + "frequent vomiting": [ + "HP:0002572" + ], + "hematochezia": [ + "HP:0002573" + ], + "rectal bleeding": [ + "HP:0002573" + ], + "recurrent rectal bleeding": [ + "HP:0002573" + ], + "episodic abdominal pain": [ + "HP:0002574" + ], + "intermittent abdominal pain": [ + "HP:0002574" + ], + "tracheoesophageal fistula": [ + "HP:0002575" + ], + "abnormal connection between trachea and esophagus": [ + "HP:0002575" + ], + "abnormal connection between trachea and oesophagus": [ + "HP:0002575" + ], + "intussusception": [ + "HP:0002576" + ], + "abnormal stomach morphology": [ + "HP:0002577" + ], + "abnormality of the stomach": [ + "HP:0002577" + ], + "gastroparesis": [ + "HP:0002578" + ], + "delay gastric empty": [ + "HP:0002578" + ], + "delayed gastric emptying": [ + "HP:0002578" + ], + "gastrointestinal dysmotility": [ + "HP:0002579" + ], + "gi dysmotility": [ + "HP:0002579" + ], + "volvulus": [ + "HP:0002580" + ], + "chronic atrophic gastritis": [ + "HP:0002582" + ], + "colitis": [ + "HP:0002583" + ], + "intestinal bleeding": [ + "HP:0002584" + ], + "intestinal haemorrhage": [ + "HP:0002584" + ], + "intestinal hemorrhage": [ + "HP:0002584" + ], + "abnormality of the peritoneum": [ + "HP:0002585" + ], + "peritonitis": [ + "HP:0002586" + ], + "inflammation of the peritoneum": [ + "HP:0002586" + ], + "projectile vomit": [ + "HP:0002587" + ], + "projectile vomiting": [ + "HP:0002587" + ], + "duodenal ulcer": [ + "HP:0002588" + ], + "gastrointestinal atresia": [ + "HP:0002589" + ], + "gi atresia": [ + "HP:0002589" + ], + "paralytic ileus": [ + "HP:0002590" + ], + "polyphagia": [ + "HP:0002591" + ], + "hyperphagia": [ + "HP:0002591" + ], + "increase appetite": [ + "HP:0002591" + ], + "increased appetite": [ + "HP:0002591" + ], + "voracious appetite": [ + "HP:0002591" + ], + "gastric ulcer": [ + "HP:0002592" + ], + "stomach ulcer": [ + "HP:0002592" + ], + "intestinal lymphangiectasia": [ + "HP:0002593" + ], + "pancreatic hypoplasia": [ + "HP:0002594" + ], + "hypoplastic pancreas": [ + "HP:0002594" + ], + "underdeveloped pancreas": [ + "HP:0002594" + ], + "ileus": [ + "HP:0002595" + ], + "gastrointestinal atony": [ + "HP:0002595" + ], + "abnormality of the vasculature": [ + "HP:0002597" + ], + "abnormality of blood vessel": [ + "HP:0002597" + ], + "abnormality of blood vessels": [ + "HP:0002597" + ], + "vascular abnormality": [ + "HP:0002597" + ], + "vascular abnormalities": [ + "HP:0002597" + ], + "head titubation": [ + "HP:0002599" + ], + "hyporeflexia of low limb": [ + "HP:0002600" + ], + "hyporeflexia of lower limbs": [ + "HP:0002600" + ], + "hyporeflexia in low limb": [ + "HP:0002600" + ], + "hyporeflexia in lower limbs": [ + "HP:0002600" + ], + "hyporeflexia of the low limb": [ + "HP:0002600" + ], + "hyporeflexia of the lower limbs": [ + "HP:0002600" + ], + "hyporeflexia , low limb": [ + "HP:0002600" + ], + "hyporeflexia , lower limbs": [ + "HP:0002600" + ], + "hyporeflexia / areflexia in low limb": [ + "HP:0002600" + ], + "hyporeflexia / areflexia in lower limbs": [ + "HP:0002600" + ], + "paresis of extensor muscle of the big toe": [ + "HP:0002601" + ], + "paresis of extensor muscles of the big toe": [ + "HP:0002601" + ], + "gastrointestinal telangiectasia": [ + "HP:0002604" + ], + "gi telangiectasia": [ + "HP:0002604" + ], + "small , enlarge blood vessel near skin": [ + "HP:0002604" + ], + "small , enlarged blood vessels near skin": [ + "HP:0002604" + ], + "hepatic necrosis": [ + "HP:0002605" + ], + "bowel incontinence": [ + "HP:0002607" + ], + "anal incontinence": [ + "HP:0002607" + ], + "faecal incontinence": [ + "HP:0002607" + ], + "fecal incontinence": [ + "HP:0002607" + ], + "loss of bowel control": [ + "HP:0002607" + ], + "celiac disease": [ + "HP:0002608" + ], + "celiac sprue": [ + "HP:0002608" + ], + "coeliac disease": [ + "HP:0002608" + ], + "coeliac sprue": [ + "HP:0002608" + ], + "cholestatic liver disease": [ + "HP:0002611" + ], + "congenital hepatic fibrosis": [ + "HP:0002612" + ], + "congenital liver fibrosis": [ + "HP:0002612" + ], + "excessive buildup of connective tissue and scarring of liver at birth": [ + "HP:0002612" + ], + "biliary cirrhosis": [ + "HP:0002613" + ], + "primary biliary cirrhosis": [ + "HP:0002613" + ], + "hepatic periportal necrosis": [ + "HP:0002614" + ], + "hypotension": [ + "HP:0002615" + ], + "arterial hypotension": [ + "HP:0002615" + ], + "low blood pressure": [ + "HP:0002615" + ], + "aortic root aneurysm": [ + "HP:0002616" + ], + "aortic root dilatation": [ + "HP:0002616" + ], + "bulge in wall of root of large artery that carry blood away from heart": [ + "HP:0002616" + ], + "bulge in wall of root of large artery that carries blood away from heart": [ + "HP:0002616" + ], + "increase aortic root diameter": [ + "HP:0002616" + ], + "increased aortic root diameter": [ + "HP:0002616" + ], + "vascular dilatation": [ + "HP:0002617" + ], + "aneurysm": [ + "HP:0002617" + ], + "aneurysmal dilatation": [ + "HP:0002617" + ], + "aneurysmal disease": [ + "HP:0002617" + ], + "aneurysms": [ + "HP:0002617" + ], + "wide than typical opening or gap": [ + "HP:0002617" + ], + "wider than typical opening or gap": [ + "HP:0002617" + ], + "varicose vein": [ + "HP:0002619" + ], + "varicose veins": [ + "HP:0002619" + ], + "atherosclerosis": [ + "HP:0002621" + ], + "atherosclerotic cardiovascular disease": [ + "HP:0002621" + ], + "narrowing and hardening of artery": [ + "HP:0002621" + ], + "narrowing and hardening of arteries": [ + "HP:0002621" + ], + "plaque build - up in artery": [ + "HP:0002621" + ], + "plaque build - up in arteries": [ + "HP:0002621" + ], + "obsolete dissect aortic dilatation": [ + "HP:0002622" + ], + "obsolete dissecting aortic dilatation": [ + "HP:0002622" + ], + "override aorta": [ + "HP:0002623" + ], + "overriding aorta": [ + "HP:0002623" + ], + "dextroposition of aorta": [ + "HP:0002623" + ], + "override aortic valve": [ + "HP:0002623" + ], + "overriding aortic valve": [ + "HP:0002623" + ], + "abnormal venous morphology": [ + "HP:0002624" + ], + "abnormal vein": [ + "HP:0002624" + ], + "venous abnormality": [ + "HP:0002624" + ], + "deep venous thrombosis": [ + "HP:0002625" + ], + "blood clot in a deep vein": [ + "HP:0002625" + ], + "deep vein thrombosis": [ + "HP:0002625" + ], + "multiple deep venous thrombosis": [ + "HP:0002625" + ], + "venous varicosity of celiac and mesenteric vessel": [ + "HP:0002626" + ], + "venous varicosities of celiac and mesenteric vessels": [ + "HP:0002626" + ], + "venous varicosity of coeliac and mesenteric vessel": [ + "HP:0002626" + ], + "venous varicosities of coeliac and mesenteric vessels": [ + "HP:0002626" + ], + "right aortic arch with mirror image branching": [ + "HP:0002627" + ], + "gastrointestinal arteriovenous malformation": [ + "HP:0002629" + ], + "gi arteriovenous malformation": [ + "HP:0002629" + ], + "fat malabsorption": [ + "HP:0002630" + ], + "obsolete dilatation of ascend aorta": [ + "HP:0002631" + ], + "obsolete dilatation of ascending aorta": [ + "HP:0002631" + ], + "low - to - normal blood pressure": [ + "HP:0002632" + ], + "low - to - normal bp": [ + "HP:0002632" + ], + "vasculitis": [ + "HP:0002633" + ], + "angiitis": [ + "HP:0002633" + ], + "inflammation of blood vessel": [ + "HP:0002633" + ], + "arteriosclerosis": [ + "HP:0002634" + ], + "harden artery wall": [ + "HP:0002634" + ], + "hardened artery wall": [ + "HP:0002634" + ], + "type iv atherosclerotic lesion": [ + "HP:0002635" + ], + "atheromatosis": [ + "HP:0002635" + ], + "dilatation of an abdominal artery": [ + "HP:0002636" + ], + "aneurysm of an abdominal artery": [ + "HP:0002636" + ], + "cerebral ischemia": [ + "HP:0002637" + ], + "brain ischemia": [ + "HP:0002637" + ], + "cerebrovascular ischemia": [ + "HP:0002637" + ], + "disruption of blood oxygen supply to brain": [ + "HP:0002637" + ], + "superficial thrombophlebitis": [ + "HP:0002638" + ], + "budd - chiari syndrome": [ + "HP:0002639" + ], + "hypertension associate with pheochromocytoma": [ + "HP:0002640" + ], + "hypertension associated with pheochromocytoma": [ + "HP:0002640" + ], + "peripheral thrombosis": [ + "HP:0002641" + ], + "peripheral blood clot": [ + "HP:0002641" + ], + "arteriovenous fistula of celiac and mesenteric vessel": [ + "HP:0002642" + ], + "arteriovenous fistulas of celiac and mesenteric vessels": [ + "HP:0002642" + ], + "arteriovenous fistula of coeliac and mesenteric vessel": [ + "HP:0002642" + ], + "arteriovenous fistulas of coeliac and mesenteric vessels": [ + "HP:0002642" + ], + "neonatal respiratory distress": [ + "HP:0002643" + ], + "infantile respiratory distress": [ + "HP:0002643" + ], + "newborn respiratory distress": [ + "HP:0002643" + ], + "respiratory distress , neonatal": [ + "HP:0002643" + ], + "abnormality of pelvic girdle bone morphology": [ + "HP:0002644" + ], + "abnormal shape of pelvic girdle bone": [ + "HP:0002644" + ], + "abnormality of the pelvic girdle": [ + "HP:0002644" + ], + "wormian bone": [ + "HP:0002645" + ], + "wormian bones": [ + "HP:0002645" + ], + "extra bone within cranial suture": [ + "HP:0002645" + ], + "extra bones within cranial sutures": [ + "HP:0002645" + ], + "intra sutural bone": [ + "HP:0002645" + ], + "intra sutural bones": [ + "HP:0002645" + ], + "intrasutural bone": [ + "HP:0002645" + ], + "intrasutural bones": [ + "HP:0002645" + ], + "island of bone within cranial suture": [ + "HP:0002645" + ], + "islands of bone within cranial sutures": [ + "HP:0002645" + ], + "aortic dissection": [ + "HP:0002647" + ], + "tear in inner wall of large artery that carry blood away from heart": [ + "HP:0002647" + ], + "tear in inner wall of large artery that carries blood away from heart": [ + "HP:0002647" + ], + "abnormality of calvarial morphology": [ + "HP:0002648" + ], + "abnormal cranium morphology": [ + "HP:0002648" + ], + "abnormality of cranial bone morphology": [ + "HP:0002648" + ], + "abnormality of skull bone morphology": [ + "HP:0002648" + ], + "abnormality of the shape of calvarium": [ + "HP:0002648" + ], + "abnormality of the shape of cranium": [ + "HP:0002648" + ], + "abnormality of the shape of skull bone": [ + "HP:0002648" + ], + "abnormality of the shape of skull bones": [ + "HP:0002648" + ], + "abnormally shape skull": [ + "HP:0002648" + ], + "abnormally shaped skull": [ + "HP:0002648" + ], + "scoliosis": [ + "HP:0002650" + ], + "spondyloepimetaphyseal dysplasia": [ + "HP:0002651" + ], + "skeletal dysplasia": [ + "HP:0002652" + ], + "abnormal skeletal development": [ + "HP:0002652" + ], + "bone pain": [ + "HP:0002653" + ], + "multiple epiphyseal dysplasia": [ + "HP:0002654" + ], + "spondyloepiphyseal dysplasia": [ + "HP:0002655" + ], + "spondyloepiphyseal dysplasia tarda": [ + "HP:0002655" + ], + "epiphyseal dysplasia": [ + "HP:0002656" + ], + "abnormal development of end part of bone": [ + "HP:0002656" + ], + "abnormal development of the end of long bone in arm and leg": [ + "HP:0002656" + ], + "abnormal development of the ends of long bones in arms and legs": [ + "HP:0002656" + ], + "spondylometaphyseal dysplasia": [ + "HP:0002657" + ], + "increase susceptibility to fracture": [ + "HP:0002659" + ], + "increased susceptibility to fractures": [ + "HP:0002659" + ], + "abnormal susceptibility to fracture": [ + "HP:0002659" + ], + "abnormal susceptibility to fractures": [ + "HP:0002659" + ], + "bone fragility": [ + "HP:0002659" + ], + "frequent break bone": [ + "HP:0002659" + ], + "frequent broken bones": [ + "HP:0002659" + ], + "increase bone fragility": [ + "HP:0002659" + ], + "increased bone fragility": [ + "HP:0002659" + ], + "increase tendency to fracture": [ + "HP:0002659" + ], + "increased tendency to fractures": [ + "HP:0002659" + ], + "painless fracture due to injury": [ + "HP:0002661" + ], + "painless fractures due to injury": [ + "HP:0002661" + ], + "delay epiphyseal ossification": [ + "HP:0002663" + ], + "delayed epiphyseal ossification": [ + "HP:0002663" + ], + "delay epiphyseal maturation": [ + "HP:0002663" + ], + "delayed epiphyseal maturation": [ + "HP:0002663" + ], + "delay maturation of end part of long bone": [ + "HP:0002663" + ], + "delayed maturation of end part of long bone": [ + "HP:0002663" + ], + "delay opacification of the epiphysis": [ + "HP:0002663" + ], + "delayed opacification of the epiphyses": [ + "HP:0002663" + ], + "epiphyseal ossification delay": [ + "HP:0002663" + ], + "neoplasm": [ + "HP:0002664" + ], + "abnormal tissue mass": [ + "HP:0002664" + ], + "cancer": [ + "HP:0002664" + ], + "neoplasia": [ + "HP:0002664" + ], + "oncological abnormality": [ + "HP:0002664" + ], + "oncology": [ + "HP:0002664" + ], + "tumor": [ + "HP:0002664" + ], + "tumour": [ + "HP:0002664" + ], + "lymphoma": [ + "HP:0002665" + ], + "cancer of lymphatic system": [ + "HP:0002665" + ], + "pheochromocytoma": [ + "HP:0002666" + ], + "chromaffin tumor": [ + "HP:0002666" + ], + "chromaffin tumors": [ + "HP:0002666" + ], + "chromaffin tumour": [ + "HP:0002666" + ], + "chromaffin tumours": [ + "HP:0002666" + ], + "nephroblastoma": [ + "HP:0002667" + ], + "wilm 's tumor": [ + "HP:0002667" + ], + "wilm 's tumour": [ + "HP:0002667" + ], + "wilms tumor": [ + "HP:0002667" + ], + "wilms tumour": [ + "HP:0002667" + ], + "paraganglioma": [ + "HP:0002668" + ], + "carotid body tumor": [ + "HP:0002668" + ], + "carotid body tumors": [ + "HP:0002668" + ], + "carotid body tumour": [ + "HP:0002668" + ], + "carotid body tumours": [ + "HP:0002668" + ], + "paragangliomas": [ + "HP:0002668" + ], + "osteosarcoma": [ + "HP:0002669" + ], + "bone cell cancer": [ + "HP:0002669" + ], + "osteogenic sarcoma": [ + "HP:0002669" + ], + "basal cell carcinoma": [ + "HP:0002671" + ], + "basal cell carcinomas": [ + "HP:0002671" + ], + "basal cell epithelioma": [ + "HP:0002671" + ], + "basal cell nevus": [ + "HP:0002671" + ], + "basalioma": [ + "HP:0002671" + ], + "gastrointestinal carcinoma": [ + "HP:0002672" + ], + "gi carcinoma": [ + "HP:0002672" + ], + "coxa valga": [ + "HP:0002673" + ], + "coxa valga deformity": [ + "HP:0002673" + ], + "cloverleaf skull": [ + "HP:0002676" + ], + "cloverleaf cranium shape": [ + "HP:0002676" + ], + "cloverleaf skull shape": [ + "HP:0002676" + ], + "kleeblattschaedel": [ + "HP:0002676" + ], + "trilobar cranium shape": [ + "HP:0002676" + ], + "trilobar skull shape": [ + "HP:0002676" + ], + "small foramen magnum": [ + "HP:0002677" + ], + "foramen magnum stenosis": [ + "HP:0002677" + ], + "hypoplasia of foramen magnum": [ + "HP:0002677" + ], + "little foramen magnum": [ + "HP:0002677" + ], + "narrow foramen magnum": [ + "HP:0002677" + ], + "stenosis of foramen magnum": [ + "HP:0002677" + ], + "skull asymmetry": [ + "HP:0002678" + ], + "abnormality of skull shape": [ + "HP:0002678" + ], + "asymmetry of skull": [ + "HP:0002678" + ], + "malformation of skull shape": [ + "HP:0002678" + ], + "unequal skull shape": [ + "HP:0002678" + ], + "uneven skull shape": [ + "HP:0002678" + ], + "abnormal sella turcica morphology": [ + "HP:0002679" + ], + "abnormality of the hypophysial fossa": [ + "HP:0002679" + ], + "abnormality of the pituitary fossa": [ + "HP:0002679" + ], + "abnormality of the sella turcica": [ + "HP:0002679" + ], + "anomaly of the hypophysial fossa": [ + "HP:0002679" + ], + "anomaly of the pituitary fossa": [ + "HP:0002679" + ], + "anomaly of the sella turcica": [ + "HP:0002679" + ], + "j - shaped sella turcica": [ + "HP:0002680" + ], + "hour glass shape hypophysial fossa": [ + "HP:0002680" + ], + "hour glass shaped hypophysial fossa": [ + "HP:0002680" + ], + "hour glass shape pituitary fossa": [ + "HP:0002680" + ], + "hour glass shaped pituitary fossa": [ + "HP:0002680" + ], + "hour glass shape sella turcica": [ + "HP:0002680" + ], + "hour glass shaped sella turcica": [ + "HP:0002680" + ], + "j - shape hypophysial fossa": [ + "HP:0002680" + ], + "j - shaped hypophysial fossa": [ + "HP:0002680" + ], + "j - shape pituitary fossa": [ + "HP:0002680" + ], + "j - shaped pituitary fossa": [ + "HP:0002680" + ], + "j - shape sella": [ + "HP:0002680" + ], + "j - shaped sella": [ + "HP:0002680" + ], + "omega shape hypophysial fossa": [ + "HP:0002680" + ], + "omega shaped hypophysial fossa": [ + "HP:0002680" + ], + "omega shape pituitary fossa": [ + "HP:0002680" + ], + "omega shaped pituitary fossa": [ + "HP:0002680" + ], + "omega shape sella turcica": [ + "HP:0002680" + ], + "omega shaped sella turcica": [ + "HP:0002680" + ], + "deform sella turcica": [ + "HP:0002681" + ], + "deformed sella turcica": [ + "HP:0002681" + ], + "abnormal shape of hypophysial fossa": [ + "HP:0002681" + ], + "abnormal shape of pituitary fossa": [ + "HP:0002681" + ], + "abnormal shape of sella turcica": [ + "HP:0002681" + ], + "deformity of hypophysial fossa": [ + "HP:0002681" + ], + "deformity of pituitary fossa": [ + "HP:0002681" + ], + "malformation of hypophysial fossa": [ + "HP:0002681" + ], + "malformation of pituitary fossa": [ + "HP:0002681" + ], + "malformation of sella turcica": [ + "HP:0002681" + ], + "broad skull": [ + "HP:0002682" + ], + "broad cranium": [ + "HP:0002682" + ], + "increase width of cranium": [ + "HP:0002682" + ], + "increased width of cranium": [ + "HP:0002682" + ], + "increase width of skull": [ + "HP:0002682" + ], + "increased width of skull": [ + "HP:0002682" + ], + "wide cranium": [ + "HP:0002682" + ], + "wide skull": [ + "HP:0002682" + ], + "abnormality of the calvaria": [ + "HP:0002683" + ], + "abnormality of calvarium": [ + "HP:0002683" + ], + "abnormality of cranial vault": [ + "HP:0002683" + ], + "abnormality of cranium": [ + "HP:0002683" + ], + "abnormality of the skull cap": [ + "HP:0002683" + ], + "abnormality of the skullcap": [ + "HP:0002683" + ], + "thicken calvaria": [ + "HP:0002684" + ], + "thickened calvaria": [ + "HP:0002684" + ], + "calvarial thickening": [ + "HP:0002684" + ], + "calvarium thicken": [ + "HP:0002684" + ], + "calvarium thickened": [ + "HP:0002684" + ], + "increase calvarial thickness": [ + "HP:0002684" + ], + "increased calvarial thickness": [ + "HP:0002684" + ], + "increased thickness of calvaria": [ + "HP:0002684" + ], + "increased thickness of calvarium": [ + "HP:0002684" + ], + "increased thickness of cranial vault": [ + "HP:0002684" + ], + "increased thickness of cranium": [ + "HP:0002684" + ], + "increased thickness of skull cap": [ + "HP:0002684" + ], + "thick calvaria": [ + "HP:0002684" + ], + "thick calvarium": [ + "HP:0002684" + ], + "thicken calvarium": [ + "HP:0002684" + ], + "thickened calvarium": [ + "HP:0002684" + ], + "thicken cranial vault": [ + "HP:0002684" + ], + "thickened cranial vault": [ + "HP:0002684" + ], + "thicken cranium": [ + "HP:0002684" + ], + "thickened cranium": [ + "HP:0002684" + ], + "thicken skull cap": [ + "HP:0002684" + ], + "thickened skull cap": [ + "HP:0002684" + ], + "thickening of the calvaria": [ + "HP:0002684" + ], + "prenatal maternal abnormality": [ + "HP:0002686" + ], + "maternal health problem": [ + "HP:0002686" + ], + "abnormality of frontal sinus": [ + "HP:0002687" + ], + "abnormality of sinus frontalis": [ + "HP:0002687" + ], + "abnormality of the forehead sinus": [ + "HP:0002687" + ], + "absent frontal sinus": [ + "HP:0002688" + ], + "absent frontal sinuses": [ + "HP:0002688" + ], + "absence of frontal sinus": [ + "HP:0002688" + ], + "absence of frontal sinuses": [ + "HP:0002688" + ], + "aplasia of frontal sinus": [ + "HP:0002688" + ], + "aplasia sinus frontalis": [ + "HP:0002688" + ], + "miss frontal sinus": [ + "HP:0002688" + ], + "missing frontal sinus": [ + "HP:0002688" + ], + "absent paranasal sinus": [ + "HP:0002689" + ], + "absent paranasal sinuses": [ + "HP:0002689" + ], + "absence of paranasal sinus": [ + "HP:0002689" + ], + "absence of paranasal sinuses": [ + "HP:0002689" + ], + "aplasia of paranasal sinus": [ + "HP:0002689" + ], + "aplasia of paranasal sinuses": [ + "HP:0002689" + ], + "miss paranasal sinus": [ + "HP:0002689" + ], + "missing paranasal sinuses": [ + "HP:0002689" + ], + "miss sinus": [ + "HP:0002689" + ], + "missing sinuses": [ + "HP:0002689" + ], + "large sella turcica": [ + "HP:0002690" + ], + "big sella turcica": [ + "HP:0002690" + ], + "enlarge sella turcica": [ + "HP:0002690" + ], + "enlarged sella turcica": [ + "HP:0002690" + ], + "hyperplasia of hypophysial fossa": [ + "HP:0002690" + ], + "hyperplasia of pituitary fossa": [ + "HP:0002690" + ], + "hyperplasia of sella turcica": [ + "HP:0002690" + ], + "large hypophysial fossa": [ + "HP:0002690" + ], + "large pituitary fossa": [ + "HP:0002690" + ], + "prominent sella turcica": [ + "HP:0002690" + ], + "platybasia": [ + "HP:0002691" + ], + "flattening of the skull base": [ + "HP:0002691" + ], + "increase basal angle of skull base": [ + "HP:0002691" + ], + "increased basal angle of skull base": [ + "HP:0002691" + ], + "obtuse basal angle of skull base": [ + "HP:0002691" + ], + "hypoplastic facial bone": [ + "HP:0002692" + ], + "hypoplastic facial bones": [ + "HP:0002692" + ], + "decreased size of facial bone": [ + "HP:0002692" + ], + "decreased size of facial bones": [ + "HP:0002692" + ], + "decreased size of facial skeleton": [ + "HP:0002692" + ], + "flattening of facial bone": [ + "HP:0002692" + ], + "flattening of facial bones": [ + "HP:0002692" + ], + "flattening of facial skeleton": [ + "HP:0002692" + ], + "hypoplasia of facial skeleton": [ + "HP:0002692" + ], + "hypotrophic facial bone": [ + "HP:0002692" + ], + "hypotrophic facial bones": [ + "HP:0002692" + ], + "hypotrophic facial skeleton": [ + "HP:0002692" + ], + "small facial bone": [ + "HP:0002692" + ], + "small facial bones": [ + "HP:0002692" + ], + "small facial skeleton": [ + "HP:0002692" + ], + "underdevelopment of facial bone": [ + "HP:0002692" + ], + "underdevelopment of facial bones": [ + "HP:0002692" + ], + "underdevelopment of facial skeleton": [ + "HP:0002692" + ], + "abnormality of the skull base": [ + "HP:0002693" + ], + "abnormality of cranial base": [ + "HP:0002693" + ], + "sclerosis of skull base": [ + "HP:0002694" + ], + "dense bone of skull base": [ + "HP:0002694" + ], + "hypercalcification of skull base": [ + "HP:0002694" + ], + "hypermineralization of skull base": [ + "HP:0002694" + ], + "hyperossification of skull base": [ + "HP:0002694" + ], + "hyperostosis of skull base": [ + "HP:0002694" + ], + "marked sclerosis of skull base": [ + "HP:0002694" + ], + "sclerosis of cranial base": [ + "HP:0002694" + ], + "sclerosis of the skull base": [ + "HP:0002694" + ], + "sclerotic skull base": [ + "HP:0002694" + ], + "symmetrical , oval parietal bone defect": [ + "HP:0002695" + ], + "symmetrical , oval parietal bone defects": [ + "HP:0002695" + ], + "symmetrical , oval defect in the parietal bone": [ + "HP:0002695" + ], + "symmetrical , oval defects in the parietal bone": [ + "HP:0002695" + ], + "abnormal parietal bone morphology": [ + "HP:0002696" + ], + "abnormality of the parietal bone": [ + "HP:0002696" + ], + "abnormality of the parietal bone of skull": [ + "HP:0002696" + ], + "parietal foramen": [ + "HP:0002697" + ], + "parietal foramina": [ + "HP:0002697" + ], + "hole in parietal bone": [ + "HP:0002697" + ], + "holes in parietal bones": [ + "HP:0002697" + ], + "opening in parietal bone": [ + "HP:0002697" + ], + "openings in parietal bones": [ + "HP:0002697" + ], + "persistent foramen of the parietal bone": [ + "HP:0002697" + ], + "persistent foramina of the parietal bones": [ + "HP:0002697" + ], + "abnormal foramen magnum morphology": [ + "HP:0002699" + ], + "abnormality of the foramen magnum": [ + "HP:0002699" + ], + "large foramen magnum": [ + "HP:0002700" + ], + "big foramen magnum": [ + "HP:0002700" + ], + "dilation of foramen magnum": [ + "HP:0002700" + ], + "enlarge foramen magnum": [ + "HP:0002700" + ], + "enlarged foramen magnum": [ + "HP:0002700" + ], + "hyperplasia of foramen magnum": [ + "HP:0002700" + ], + "increase circumference of foramen magnum": [ + "HP:0002700" + ], + "increased circumference of foramen magnum": [ + "HP:0002700" + ], + "increase diameter of foramen magnum": [ + "HP:0002700" + ], + "increased diameter of foramen magnum": [ + "HP:0002700" + ], + "wide foramen magnum": [ + "HP:0002700" + ], + "abnormality of skull ossification": [ + "HP:0002703" + ], + "abnormality of bone calcification of calvarium": [ + "HP:0002703" + ], + "abnormality of bone calcification of cranium": [ + "HP:0002703" + ], + "abnormality of bone calcification of skull": [ + "HP:0002703" + ], + "abnormality of bone formation of calvarium": [ + "HP:0002703" + ], + "abnormality of bone formation of cranium": [ + "HP:0002703" + ], + "abnormality of bone mineralization of calvarium": [ + "HP:0002703" + ], + "abnormality of bone mineralization of cranium": [ + "HP:0002703" + ], + "abnormality of bone mineralization of skull": [ + "HP:0002703" + ], + "abnormality of ossification of calvarium": [ + "HP:0002703" + ], + "abnormality of ossification of cranium": [ + "HP:0002703" + ], + "abnormality of skull bone formation": [ + "HP:0002703" + ], + "high , narrow palate": [ + "HP:0002705" + ], + "gothic palate": [ + "HP:0002705" + ], + "high narrow palate": [ + "HP:0002705" + ], + "high vault palate": [ + "HP:0002705" + ], + "high vaulted palate": [ + "HP:0002705" + ], + "narrow and high arch palate": [ + "HP:0002705" + ], + "narrow and high arched palate": [ + "HP:0002705" + ], + "narrow , high - arched palate": [ + "HP:0002705" + ], + "narrow , high - arch roof of mouth": [ + "HP:0002705" + ], + "narrow , high - arched roof of mouth": [ + "HP:0002705" + ], + "narrow , highly arched palate": [ + "HP:0002705" + ], + "narrow , highly arched roof of mouth": [ + "HP:0002705" + ], + "palate telangiectasia": [ + "HP:0002707" + ], + "palatal angioectasia": [ + "HP:0002707" + ], + "palatal spider vein": [ + "HP:0002707" + ], + "palatal spider veins": [ + "HP:0002707" + ], + "palatal telangiectasia": [ + "HP:0002707" + ], + "palate telangiectases": [ + "HP:0002707" + ], + "palate teleangiectases": [ + "HP:0002707" + ], + "spider vein of the roof of the mouth": [ + "HP:0002707" + ], + "spider veins of the roof of the mouth": [ + "HP:0002707" + ], + "telangiectasia of the roof of the mouth": [ + "HP:0002707" + ], + "prominent median palatal raphe": [ + "HP:0002708" + ], + "prominent central palatal ridge": [ + "HP:0002708" + ], + "prominent central ridge on roof of the mouth": [ + "HP:0002708" + ], + "prominent medial palatal suture": [ + "HP:0002708" + ], + "commissural lip pit": [ + "HP:0002710" + ], + "commissural labial pit": [ + "HP:0002710" + ], + "commissural labial pits": [ + "HP:0002710" + ], + "commissural pit": [ + "HP:0002710" + ], + "lip pit at corner of the mouth": [ + "HP:0002710" + ], + "lip pits at corners of the mouth": [ + "HP:0002710" + ], + "pit at the corner of the lip": [ + "HP:0002710" + ], + "pits at the corners of the lips": [ + "HP:0002710" + ], + "exaggerated median tongue furrow": [ + "HP:0002711" + ], + "deep central lingual furrow": [ + "HP:0002711" + ], + "deep central lingual groove": [ + "HP:0002711" + ], + "deep central tongue furrow": [ + "HP:0002711" + ], + "deep central tongue groove": [ + "HP:0002711" + ], + "deep median lingual furrow": [ + "HP:0002711" + ], + "deep median lingual groove": [ + "HP:0002711" + ], + "deep median tongue furrow": [ + "HP:0002711" + ], + "deep median tongue groove": [ + "HP:0002711" + ], + "exaggerated median lingual furrow": [ + "HP:0002711" + ], + "downturned corner of mouth": [ + "HP:0002714" + ], + "downturned corners of mouth": [ + "HP:0002714" + ], + "downturned corner of the mouth": [ + "HP:0002714" + ], + "downturned corners of the mouth": [ + "HP:0002714" + ], + "downturned mouth": [ + "HP:0002714" + ], + "downturned oral commisures": [ + "HP:0002714" + ], + "abnormality of the immune system": [ + "HP:0002715" + ], + "immunological abnormality": [ + "HP:0002715" + ], + "lymphadenopathy": [ + "HP:0002716" + ], + "lymph node hyperplasia": [ + "HP:0002716" + ], + "swollen lymph node": [ + "HP:0002716" + ], + "swollen lymph nodes": [ + "HP:0002716" + ], + "adrenal overactivity": [ + "HP:0002717" + ], + "recurrent bacterial infection": [ + "HP:0002718" + ], + "recurrent bacterial infections": [ + "HP:0002718" + ], + "bacterial infection , recurrent": [ + "HP:0002718" + ], + "bacterial infections , recurrent": [ + "HP:0002718" + ], + "frequent bacterial infection": [ + "HP:0002718" + ], + "frequent bacterial infections": [ + "HP:0002718" + ], + "frequent pyogenic infection": [ + "HP:0002718" + ], + "frequent pyogenic infections": [ + "HP:0002718" + ], + "increase susceptibility to bacterial infection": [ + "HP:0002718" + ], + "increased susceptibility to bacterial infections": [ + "HP:0002718" + ], + "prone to bacterial infection": [ + "HP:0002718" + ], + "recurrent major bacterial infection": [ + "HP:0002718" + ], + "recurrent major bacterial infections": [ + "HP:0002718" + ], + "recurrent pyogenic infection": [ + "HP:0002718" + ], + "recurrent pyogenic infections": [ + "HP:0002718" + ], + "susceptibility to pyogenic infection": [ + "HP:0002718" + ], + "recurrent infection": [ + "HP:0002719" + ], + "recurrent infections": [ + "HP:0002719" + ], + "frequent infection": [ + "HP:0002719" + ], + "frequent infections": [ + "HP:0002719" + ], + "frequent , severe infection": [ + "HP:0002719" + ], + "frequent , severe infections": [ + "HP:0002719" + ], + "increased frequency of infection": [ + "HP:0002719" + ], + "infection , recurrent": [ + "HP:0002719" + ], + "infections , recurrent": [ + "HP:0002719" + ], + "predisposition to infection": [ + "HP:0002719" + ], + "predisposition to infections": [ + "HP:0002719" + ], + "susceptibility to infection": [ + "HP:0002719" + ], + "decrease circulate iga level": [ + "HP:0002720" + ], + "decreased circulating iga level": [ + "HP:0002720" + ], + "decrease iga": [ + "HP:0002720" + ], + "decreased iga": [ + "HP:0002720" + ], + "decrease immunoglobulin a": [ + "HP:0002720" + ], + "decreased immunoglobulin a": [ + "HP:0002720" + ], + "gamma - a globulin deficiency": [ + "HP:0002720" + ], + "iga deficiency": [ + "HP:0002720" + ], + "low level of immunoglobulin a": [ + "HP:0002720" + ], + "low levels of immunoglobulin a": [ + "HP:0002720" + ], + "reduce iga level": [ + "HP:0002720" + ], + "reduced iga levels": [ + "HP:0002720" + ], + "immunodeficiency": [ + "HP:0002721" + ], + "decrease immune function": [ + "HP:0002721" + ], + "decreased immune function": [ + "HP:0002721" + ], + "immune deficiency": [ + "HP:0002721" + ], + "recurrent abscess formation": [ + "HP:0002722" + ], + "absence of bactericidal oxidative respiratory burst in phagocyte": [ + "HP:0002723" + ], + "absence of bactericidal oxidative respiratory burst in phagocytes": [ + "HP:0002723" + ], + "recurrent aspergillus infection": [ + "HP:0002724" + ], + "recurrent aspergillus infections": [ + "HP:0002724" + ], + "aspergillus infection , recurrent": [ + "HP:0002724" + ], + "aspergillus infections , recurrent": [ + "HP:0002724" + ], + "systemic lupus erythematosus": [ + "HP:0002725" + ], + "recurrent staphylococcus aureus infection": [ + "HP:0002726" + ], + "recurrent staphylococcus aureus infections": [ + "HP:0002726" + ], + "staphylococcus aureus infection , recurrent": [ + "HP:0002726" + ], + "staphylococcus aureus infections , recurrent": [ + "HP:0002726" + ], + "chronic mucocutaneous candidiasis": [ + "HP:0002728" + ], + "chronic candidiasis of mucosa , skin and nail": [ + "HP:0002728" + ], + "chronic candidiasis of mucosa , skin and nails": [ + "HP:0002728" + ], + "mucocutaneous candidiasis": [ + "HP:0002728" + ], + "follicular hyperplasia": [ + "HP:0002729" + ], + "chronic noninfectious lymphadenopathy": [ + "HP:0002730" + ], + "decrease lymphocyte apoptosis": [ + "HP:0002731" + ], + "decreased lymphocyte apoptosis": [ + "HP:0002731" + ], + "defective lymphocyte apoptosis": [ + "HP:0002731" + ], + "lymph node hypoplasia": [ + "HP:0002732" + ], + "small lymph node": [ + "HP:0002732" + ], + "small lymph nodes": [ + "HP:0002732" + ], + "abnormality of the lymph node": [ + "HP:0002733" + ], + "abnormality of the lymph nodes": [ + "HP:0002733" + ], + "abnormal lymph node histology": [ + "HP:0002733" + ], + "thick skull base": [ + "HP:0002737" + ], + "increased thickness of bone of skull base": [ + "HP:0002737" + ], + "increased thickness of skull base": [ + "HP:0002737" + ], + "hypoplastic frontal sinus": [ + "HP:0002738" + ], + "hypoplastic frontal sinuses": [ + "HP:0002738" + ], + "decreased pneumatization of frontal sinus": [ + "HP:0002738" + ], + "decreased volume of frontal sinus": [ + "HP:0002738" + ], + "decreased volume of frontal sinuses": [ + "HP:0002738" + ], + "hypotrophic frontal sinus": [ + "HP:0002738" + ], + "small frontal sinus": [ + "HP:0002738" + ], + "small frontal sinuses": [ + "HP:0002738" + ], + "underdeveloped frontal sinus": [ + "HP:0002738" + ], + "underdeveloped frontal sinuses": [ + "HP:0002738" + ], + "recurrent e. coli infection": [ + "HP:0002740" + ], + "recurrent e. coli infections": [ + "HP:0002740" + ], + "e coli infection": [ + "HP:0002740" + ], + "e coli infections": [ + "HP:0002740" + ], + "e coli infection , recurrent": [ + "HP:0002740" + ], + "e coli infections , recurrent": [ + "HP:0002740" + ], + "recurrent serratia marcescens infection": [ + "HP:0002741" + ], + "recurrent serratia marcescens infections": [ + "HP:0002741" + ], + "recurrent klebsiella infection": [ + "HP:0002742" + ], + "recurrent klebsiella infections": [ + "HP:0002742" + ], + "klebsiella infection , recurrent": [ + "HP:0002742" + ], + "klebsiella infections , recurrent": [ + "HP:0002742" + ], + "recurrent enteroviral infection": [ + "HP:0002743" + ], + "recurrent enteroviral infections": [ + "HP:0002743" + ], + "bilateral cleft lip and palate": [ + "HP:0002744" + ], + "bilateral cleft lip and cleft palate": [ + "HP:0002744" + ], + "right and leave cleft lip and palate": [ + "HP:0002744" + ], + "right and left cleft lip and palate": [ + "HP:0002744" + ], + "oral leukoplakia": [ + "HP:0002745" + ], + "leukokeratosis": [ + "HP:0002745" + ], + "oral idiopathic keratosis": [ + "HP:0002745" + ], + "oral idiopathic leukoplakia": [ + "HP:0002745" + ], + "oral idiopathic white patch": [ + "HP:0002745" + ], + "oral leucoplakia": [ + "HP:0002745" + ], + "oral leukokeratosis": [ + "HP:0002745" + ], + "oral leukoplasia": [ + "HP:0002745" + ], + "oral white patch": [ + "HP:0002745" + ], + "oral white plaque": [ + "HP:0002745" + ], + "respiratory insufficiency due to muscle weakness": [ + "HP:0002747" + ], + "decrease lung function due to weak breathing muscle": [ + "HP:0002747" + ], + "decreased lung function due to weak breathing muscles": [ + "HP:0002747" + ], + "decreased respiratory function due to muscle weakness": [ + "HP:0002747" + ], + "respiratory distress due to muscle weakness": [ + "HP:0002747" + ], + "respiratory failure due to muscle weakness": [ + "HP:0002747" + ], + "respiratory muscle weakness": [ + "HP:0002747" + ], + "rickets": [ + "HP:0002748" + ], + "weak and soft bone": [ + "HP:0002748" + ], + "weak and soft bones": [ + "HP:0002748" + ], + "osteomalacia": [ + "HP:0002749" + ], + "softening of the bone": [ + "HP:0002749" + ], + "softening of the bones": [ + "HP:0002749" + ], + "delay skeletal maturation": [ + "HP:0002750" + ], + "delayed skeletal maturation": [ + "HP:0002750" + ], + "delay bone age": [ + "HP:0002750" + ], + "delayed bone age": [ + "HP:0002750" + ], + "delay bone age before puberty": [ + "HP:0002750" + ], + "delayed bone age before puberty": [ + "HP:0002750" + ], + "delay bone maturation": [ + "HP:0002750" + ], + "delayed bone maturation": [ + "HP:0002750" + ], + "delay skeletal development": [ + "HP:0002750" + ], + "delayed skeletal development": [ + "HP:0002750" + ], + "retard bone age": [ + "HP:0002750" + ], + "retarded bone age": [ + "HP:0002750" + ], + "retard ossification": [ + "HP:0002750" + ], + "retarded ossification": [ + "HP:0002750" + ], + "skeletal maturation retardation": [ + "HP:0002750" + ], + "kyphoscoliosis": [ + "HP:0002751" + ], + "sparse bone trabecula": [ + "HP:0002752" + ], + "sparse bone trabeculae": [ + "HP:0002752" + ], + "thin bony cortex": [ + "HP:0002753" + ], + "thin cortex": [ + "HP:0002753" + ], + "thin cortices": [ + "HP:0002753" + ], + "osteomyelitis": [ + "HP:0002754" + ], + "bone infection": [ + "HP:0002754" + ], + "obsolete osteomyelitis due to immunodeficiency": [ + "HP:0002755" + ], + "pathologic fracture": [ + "HP:0002756" + ], + "pathologic fractures": [ + "HP:0002756" + ], + "spontaneous fracture": [ + "HP:0002756" + ], + "spontaneous fractures": [ + "HP:0002756" + ], + "recurrent fracture": [ + "HP:0002757" + ], + "recurrent fractures": [ + "HP:0002757" + ], + "frequent fracture": [ + "HP:0002757" + ], + "frequent fractures": [ + "HP:0002757" + ], + "increased fracture rate": [ + "HP:0002757" + ], + "increase fracture": [ + "HP:0002757" + ], + "increased fractures": [ + "HP:0002757" + ], + "multiple fracture": [ + "HP:0002757" + ], + "multiple fractures": [ + "HP:0002757" + ], + "multiple spontaneous fracture": [ + "HP:0002757" + ], + "multiple spontaneous fractures": [ + "HP:0002757" + ], + "vary degree of multiple fracture": [ + "HP:0002757" + ], + "varying degree of multiple fractures": [ + "HP:0002757" + ], + "osteoarthritis": [ + "HP:0002758" + ], + "degenerative joint disease": [ + "HP:0002758" + ], + "generalize joint laxity": [ + "HP:0002761" + ], + "generalized joint laxity": [ + "HP:0002761" + ], + "generalise joint laxity": [ + "HP:0002761" + ], + "generalised joint laxity": [ + "HP:0002761" + ], + "hypermobility of all joint": [ + "HP:0002761" + ], + "hypermobility of all joints": [ + "HP:0002761" + ], + "joint laxity , generalise": [ + "HP:0002761" + ], + "joint laxity , generalised": [ + "HP:0002761" + ], + "joint laxity , generalize": [ + "HP:0002761" + ], + "joint laxity , generalized": [ + "HP:0002761" + ], + "multiple exostosis": [ + "HP:0002762" + ], + "multiple exostoses": [ + "HP:0002762" + ], + "abnormal cartilage morphology": [ + "HP:0002763" + ], + "abnormal shape of cartilage": [ + "HP:0002763" + ], + "abnormality of cartilage morphology": [ + "HP:0002763" + ], + "stipple chondral calcification": [ + "HP:0002764" + ], + "stippled chondral calcification": [ + "HP:0002764" + ], + "relatively short spine": [ + "HP:0002766" + ], + "obsolete small vertebral body": [ + "HP:0002773" + ], + "obsolete small vertebral bodies": [ + "HP:0002773" + ], + "tracheal stenosis": [ + "HP:0002777" + ], + "narrowing of windpipe": [ + "HP:0002777" + ], + "abnormal tracheal morphology": [ + "HP:0002778" + ], + "abnormal trachea morphology": [ + "HP:0002778" + ], + "abnormality of the trachea": [ + "HP:0002778" + ], + "tracheal disease": [ + "HP:0002778" + ], + "tracheomalacia": [ + "HP:0002779" + ], + "floppy windpipe": [ + "HP:0002779" + ], + "bronchomalacia": [ + "HP:0002780" + ], + "upper airway obstruction": [ + "HP:0002781" + ], + "recurrent low respiratory tract infection": [ + "HP:0002783" + ], + "recurrent lower respiratory tract infections": [ + "HP:0002783" + ], + "chronic lung infection": [ + "HP:0002783" + ], + "chronic lung infections": [ + "HP:0002783" + ], + "low respiratory tract infection": [ + "HP:0002783" + ], + "lower respiratory tract infections": [ + "HP:0002783" + ], + "recurrent chest infection": [ + "HP:0002783" + ], + "recurrent chest infections": [ + "HP:0002783" + ], + "tracheobronchomalacia": [ + "HP:0002786" + ], + "tracheal calcification": [ + "HP:0002787" + ], + "calcification of the trachea": [ + "HP:0002787" + ], + "tracheal calcifications": [ + "HP:0002787" + ], + "tracheal ectopic calcification": [ + "HP:0002787" + ], + "recurrent upper respiratory tract infection": [ + "HP:0002788" + ], + "recurrent upper respiratory tract infections": [ + "HP:0002788" + ], + "frequent upper respiratory infection": [ + "HP:0002788" + ], + "frequent upper respiratory infections": [ + "HP:0002788" + ], + "frequent upper respiratory tract infection": [ + "HP:0002788" + ], + "frequent upper respiratory tract infections": [ + "HP:0002788" + ], + "recurrent cold": [ + "HP:0002788" + ], + "recurrent colds": [ + "HP:0002788" + ], + "recurrent upper respiratory and low respiratory infection": [ + "HP:0002788" + ], + "recurrent upper respiratory and lower respiratory infections": [ + "HP:0002788" + ], + "recurrent upper respiratory infection": [ + "HP:0002788" + ], + "recurrent upper respiratory infections": [ + "HP:0002788" + ], + "recurrent uri": [ + "HP:0002788" + ], + "upper respiratory tract infection": [ + "HP:0002788" + ], + "upper respiratory tract infections": [ + "HP:0002788" + ], + "upper respiratory tract infection , recurrent": [ + "HP:0002788" + ], + "upper respiratory tract infections , recurrent": [ + "HP:0002788" + ], + "tachypnea": [ + "HP:0002789" + ], + "increase respiratory rate or depth of breathe": [ + "HP:0002789" + ], + "increased respiratory rate or depth of breathing": [ + "HP:0002789" + ], + "polypnea": [ + "HP:0002789" + ], + "neonatal breathing dysregulation": [ + "HP:0002790" + ], + "impaired breathing in newborn": [ + "HP:0002790" + ], + "hypoventilation": [ + "HP:0002791" + ], + "alveolar hypoventilation": [ + "HP:0002791" + ], + "respiratory depression": [ + "HP:0002791" + ], + "slow breathing": [ + "HP:0002791" + ], + "under breathe": [ + "HP:0002791" + ], + "under breathing": [ + "HP:0002791" + ], + "reduce vital capacity": [ + "HP:0002792" + ], + "reduced vital capacity": [ + "HP:0002792" + ], + "decrease vital capacity": [ + "HP:0002792" + ], + "decreased vital capacity": [ + "HP:0002792" + ], + "abnormal pattern of respiration": [ + "HP:0002793" + ], + "abnormal respiratory pattern": [ + "HP:0002793" + ], + "abnormal respiratory patterns": [ + "HP:0002793" + ], + "unusual breathing pattern": [ + "HP:0002793" + ], + "unusual breathing patterns": [ + "HP:0002793" + ], + "abnormal respiratory system physiology": [ + "HP:0002795" + ], + "abnormal respiration": [ + "HP:0002795" + ], + "functional respiratory abnormality": [ + "HP:0002795" + ], + "respiratory problem": [ + "HP:0002795" + ], + "osteolysis": [ + "HP:0002797" + ], + "breakdown of bone": [ + "HP:0002797" + ], + "increase bone resorption": [ + "HP:0002797" + ], + "increased bone resorption": [ + "HP:0002797" + ], + "osteolytic defect of bone": [ + "HP:0002797" + ], + "osteolytic defects of bones": [ + "HP:0002797" + ], + "congenital contracture": [ + "HP:0002803" + ], + "congenital contractures": [ + "HP:0002803" + ], + "congenital joint contracture": [ + "HP:0002803" + ], + "congenital joint contractures": [ + "HP:0002803" + ], + "arthrogryposis multiplex congenita": [ + "HP:0002804" + ], + "arthrogryposis": [ + "HP:0002804" + ], + "arthrogryposis multiplex": [ + "HP:0002804" + ], + "arthrogryposis , congenital": [ + "HP:0002804" + ], + "multiple congenital contracture": [ + "HP:0002804" + ], + "multiple congenital contractures": [ + "HP:0002804" + ], + "accelerate bone age after puberty": [ + "HP:0002805" + ], + "accelerated bone age after puberty": [ + "HP:0002805" + ], + "kyphosis": [ + "HP:0002808" + ], + "gibbus deformity": [ + "HP:0002808" + ], + "hunch back": [ + "HP:0002808" + ], + "hunched back": [ + "HP:0002808" + ], + "hyperkyphosis": [ + "HP:0002808" + ], + "round back": [ + "HP:0002808" + ], + "dumbbell - shaped metaphyses": [ + "HP:0002810" + ], + "dumbbell shape metaphyses": [ + "HP:0002810" + ], + "dumbbell shaped metaphyses": [ + "HP:0002810" + ], + "dumbbell shape metaphysis": [ + "HP:0002810" + ], + "dumbbell shaped metaphysis": [ + "HP:0002810" + ], + "dumbbell shape wide portion of long bone": [ + "HP:0002810" + ], + "dumbbell shaped wide portion of long bone": [ + "HP:0002810" + ], + "coxa vara": [ + "HP:0002812" + ], + "abnormality of limb bone morphology": [ + "HP:0002813" + ], + "abnormal shape of limb bone": [ + "HP:0002813" + ], + "arm and / or leg bone difference": [ + "HP:0002813" + ], + "arm and / or leg bone differences": [ + "HP:0002813" + ], + "limb abnormality": [ + "HP:0002813" + ], + "abnormality of the low limb": [ + "HP:0002814" + ], + "abnormality of the lower limb": [ + "HP:0002814" + ], + "abnormality of the leg": [ + "HP:0002814" + ], + "low limb deformity": [ + "HP:0002814" + ], + "lower limb deformities": [ + "HP:0002814" + ], + "abnormality of the knee": [ + "HP:0002815" + ], + "genu recurvatum": [ + "HP:0002816" + ], + "back knee": [ + "HP:0002816" + ], + "genu recurvata": [ + "HP:0002816" + ], + "knee hyperextension": [ + "HP:0002816" + ], + "abnormality of the upper limb": [ + "HP:0002817" + ], + "abnormality of the arm": [ + "HP:0002817" + ], + "abnormality of the radius": [ + "HP:0002818" + ], + "neuropathic arthropathy": [ + "HP:0002821" + ], + "charcot arthropathy": [ + "HP:0002821" + ], + "charcot joint": [ + "HP:0002821" + ], + "hyperplasia of the femoral trochanter": [ + "HP:0002822" + ], + "hyperplasia of the femoral trochanters": [ + "HP:0002822" + ], + "hyperplastic femoral trochanter": [ + "HP:0002822" + ], + "hyperplastic femoral trochanters": [ + "HP:0002822" + ], + "abnormality of femur morphology": [ + "HP:0002823" + ], + "abnormality of the femur": [ + "HP:0002823" + ], + "abnormality of the femora": [ + "HP:0002823" + ], + "abnormality of the thighbone": [ + "HP:0002823" + ], + "caudal appendage": [ + "HP:0002825" + ], + "coccygeal tail": [ + "HP:0002825" + ], + "human tail": [ + "HP:0002825" + ], + "halberd - shape pelvis": [ + "HP:0002826" + ], + "halberd - shaped pelvis": [ + "HP:0002826" + ], + "halberd - shape pelvis bone": [ + "HP:0002826" + ], + "halberd - shaped pelvis bone": [ + "HP:0002826" + ], + "hip dislocation": [ + "HP:0002827" + ], + "dislocate hip": [ + "HP:0002827" + ], + "dislocated hips": [ + "HP:0002827" + ], + "dislocation of hip": [ + "HP:0002827" + ], + "multiple joint contracture": [ + "HP:0002828" + ], + "multiple joint contractures": [ + "HP:0002828" + ], + "arthralgia": [ + "HP:0002829" + ], + "arthralgias": [ + "HP:0002829" + ], + "arthritic pain": [ + "HP:0002829" + ], + "joint pain": [ + "HP:0002829" + ], + "joint pains": [ + "HP:0002829" + ], + "long coccyx": [ + "HP:0002831" + ], + "long tailbone": [ + "HP:0002831" + ], + "calcific stipple": [ + "HP:0002832" + ], + "calcific stippling": [ + "HP:0002832" + ], + "discrete calcific stipple": [ + "HP:0002832" + ], + "discrete calcific stippling": [ + "HP:0002832" + ], + "cystic angiomatosis of bone": [ + "HP:0002833" + ], + "lytic cystic lesion in appendicular bone": [ + "HP:0002833" + ], + "lytic cystic lesions in appendicular bones": [ + "HP:0002833" + ], + "flared femoral metaphysis": [ + "HP:0002834" + ], + "flared metaphysis of thigh bone": [ + "HP:0002834" + ], + "aspiration": [ + "HP:0002835" + ], + "pulmonary aspiration": [ + "HP:0002835" + ], + "bladder exstrophy": [ + "HP:0002836" + ], + "ectopia vesica": [ + "HP:0002836" + ], + "ectopia vesicae": [ + "HP:0002836" + ], + "recurrent bronchitis": [ + "HP:0002837" + ], + "bronchitis , recurrent": [ + "HP:0002837" + ], + "urinary bladder sphincter dysfunction": [ + "HP:0002839" + ], + "sphincter disturbance": [ + "HP:0002839" + ], + "sphincter disturbances": [ + "HP:0002839" + ], + "lymphadenitis": [ + "HP:0002840" + ], + "inflammation of the lymph node": [ + "HP:0002840" + ], + "inflammation of the lymph nodes": [ + "HP:0002840" + ], + "recurrent fungal infection": [ + "HP:0002841" + ], + "recurrent fungal infections": [ + "HP:0002841" + ], + "recurrent burkholderia cepacia infection": [ + "HP:0002842" + ], + "recurrent burkholderia cepacia infections": [ + "HP:0002842" + ], + "abnormal t cell morphology": [ + "HP:0002843" + ], + "abnormal t cell": [ + "HP:0002843" + ], + "abnormal t cells": [ + "HP:0002843" + ], + "abnormality of t cell": [ + "HP:0002843" + ], + "abnormality of t cells": [ + "HP:0002843" + ], + "cellular immune defect": [ + "HP:0002843" + ], + "defective cellular immunity": [ + "HP:0002843" + ], + "obsolete increase proportion of peripheral cd3+ t cell": [ + "HP:0002845" + ], + "obsolete increased proportion of peripheral cd3+ t cells": [ + "HP:0002845" + ], + "abnormal b cell morphology": [ + "HP:0002846" + ], + "abnormal b cell": [ + "HP:0002846" + ], + "abnormal b cells": [ + "HP:0002846" + ], + "abnormality of b cell": [ + "HP:0002846" + ], + "abnormality of b cells": [ + "HP:0002846" + ], + "impaired memory b cell generation": [ + "HP:0002847" + ], + "decrease specific anti - polysaccharide antibody level": [ + "HP:0002848" + ], + "decreased specific anti - polysaccharide antibody level": [ + "HP:0002848" + ], + "depress antibody response to polysaccharide antigen": [ + "HP:0002848" + ], + "depressed antibody response to polysaccharide antigens": [ + "HP:0002848" + ], + "low specific anti - polysaccharide antibody titer": [ + "HP:0002848" + ], + "specific anti - polysaccharide antibody deficiency": [ + "HP:0002848" + ], + "absence of lymph node germinal center": [ + "HP:0002849" + ], + "absence of lymph node germinal centre": [ + "HP:0002849" + ], + "lymph node lack germinal center": [ + "HP:0002849" + ], + "lymph nodes lack germinal center": [ + "HP:0002849" + ], + "lymph node lack germinal centre": [ + "HP:0002849" + ], + "lymph nodes lack germinal centre": [ + "HP:0002849" + ], + "lymphoid germinal center defect": [ + "HP:0002849" + ], + "lymphoid germinal centre defect": [ + "HP:0002849" + ], + "decrease circulate total igm": [ + "HP:0002850" + ], + "decreased circulating total igm": [ + "HP:0002850" + ], + "decrease igm": [ + "HP:0002850" + ], + "decreased igm": [ + "HP:0002850" + ], + "decrease igm level": [ + "HP:0002850" + ], + "decreased igm level": [ + "HP:0002850" + ], + "igm deficiency": [ + "HP:0002850" + ], + "reduce igm level": [ + "HP:0002850" + ], + "reduced igm levels": [ + "HP:0002850" + ], + "elevate proportion of cd4 - negative , cd8 - negative , alpha - beta regulatory t cell": [ + "HP:0002851" + ], + "elevated proportion of cd4 - negative , cd8 - negative , alpha - beta regulatory t cells": [ + "HP:0002851" + ], + "increased number of cd4 - / cd8 - t cell express alpha / beta t - cell receptor": [ + "HP:0002851" + ], + "increased number of cd4 - / cd8 - t cells expressing alpha / beta t - cell receptors": [ + "HP:0002851" + ], + "increase proportion of hla dr+ t cell": [ + "HP:0002853" + ], + "increased proportion of hla dr+ t cells": [ + "HP:0002853" + ], + "genu valgum": [ + "HP:0002857" + ], + "genu valga": [ + "HP:0002857" + ], + "genu valgus": [ + "HP:0002857" + ], + "genua valga": [ + "HP:0002857" + ], + "knee joint valgus deformity": [ + "HP:0002857" + ], + "knock knee": [ + "HP:0002857" + ], + "knock knees": [ + "HP:0002857" + ], + "meningioma": [ + "HP:0002858" + ], + "noncancerous growth of membrane cover brain": [ + "HP:0002858" + ], + "noncancerous growth of membranes covering brain": [ + "HP:0002858" + ], + "rhabdomyosarcoma": [ + "HP:0002859" + ], + "squamous cell carcinoma": [ + "HP:0002860" + ], + "squamous cell cancer": [ + "HP:0002860" + ], + "melanoma": [ + "HP:0002861" + ], + "cancer of skin pigment cell": [ + "HP:0002861" + ], + "cancer of skin pigment cells": [ + "HP:0002861" + ], + "malignant melanoma": [ + "HP:0002861" + ], + "skin cancer ( melanoma )": [ + "HP:0002861" + ], + "bladder carcinoma": [ + "HP:0002862" + ], + "myelodysplasia": [ + "HP:0002863" + ], + "hypoplastic myelodysplasia": [ + "HP:0002863" + ], + "myelodysplastic syndrome": [ + "HP:0002863" + ], + "paraganglioma of head and neck": [ + "HP:0002864" + ], + "paragangliomas , head and neck": [ + "HP:0002864" + ], + "medullary thyroid carcinoma": [ + "HP:0002865" + ], + "medullary thyroid cancer": [ + "HP:0002865" + ], + "hypoplastic iliac wing": [ + "HP:0002866" + ], + "hypoplastic iliac ala": [ + "HP:0002866" + ], + "hypoplastic iliac alae": [ + "HP:0002866" + ], + "hypoplastic iliac wings": [ + "HP:0002866" + ], + "small iliac wing": [ + "HP:0002866" + ], + "small iliac wings": [ + "HP:0002866" + ], + "abnormal ilium morphology": [ + "HP:0002867" + ], + "abnormality of the ilium": [ + "HP:0002867" + ], + "iliac abnormality": [ + "HP:0002867" + ], + "iliac abnormalities": [ + "HP:0002867" + ], + "narrow iliac wing": [ + "HP:0002868" + ], + "narrow iliac wings": [ + "HP:0002868" + ], + "flare iliac wing": [ + "HP:0002869" + ], + "flared iliac wing": [ + "HP:0002869" + ], + "flared iliac wings": [ + "HP:0002869" + ], + "obstructive sleep apnea": [ + "HP:0002870" + ], + "obstructive sleep apnoea": [ + "HP:0002870" + ], + "central apnea": [ + "HP:0002871" + ], + "central apnoea": [ + "HP:0002871" + ], + "apneic episode precipitate by illness , fatigue , stress": [ + "HP:0002872" + ], + "apneic episodes precipitated by illness , fatigue , stress": [ + "HP:0002872" + ], + "episodic apnea induce by febrile illness or stress": [ + "HP:0002872" + ], + "episodic apnea induced by febrile illness or stress": [ + "HP:0002872" + ], + "exertional dyspnea": [ + "HP:0002875" + ], + "exertional breathlessness": [ + "HP:0002875" + ], + "exertional dyspnoea": [ + "HP:0002875" + ], + "shortness of breathe upon physical activity": [ + "HP:0002875" + ], + "shortness of breathing upon physical activity": [ + "HP:0002875" + ], + "episodic tachypnea": [ + "HP:0002876" + ], + "hyperpnea , episodic": [ + "HP:0002876" + ], + "nocturnal hypoventilation": [ + "HP:0002877" + ], + "hypoventilation during sleep": [ + "HP:0002877" + ], + "nocturnal hypopnea": [ + "HP:0002877" + ], + "nocturnal slow breathing": [ + "HP:0002877" + ], + "nocturnal under breathe": [ + "HP:0002877" + ], + "nocturnal under breathing": [ + "HP:0002877" + ], + "respiratory failure": [ + "HP:0002878" + ], + "anisospondyly": [ + "HP:0002879" + ], + "obsolete respiratory difficulty": [ + "HP:0002880" + ], + "obsolete respiratory difficulties": [ + "HP:0002880" + ], + "sudden episodic apnea": [ + "HP:0002882" + ], + "hyperventilation": [ + "HP:0002883" + ], + "rapid breathing": [ + "HP:0002883" + ], + "hepatoblastoma": [ + "HP:0002884" + ], + "medulloblastoma": [ + "HP:0002885" + ], + "vagal paraganglioma": [ + "HP:0002886" + ], + "glomus vagale paraganglioma": [ + "HP:0002886" + ], + "glomus vagale tumor": [ + "HP:0002886" + ], + "glomus vagale tumour": [ + "HP:0002886" + ], + "vagal nerve tumor": [ + "HP:0002886" + ], + "vagal nerve tumors": [ + "HP:0002886" + ], + "vagal nerve tumour": [ + "HP:0002886" + ], + "vagal nerve tumours": [ + "HP:0002886" + ], + "ependymoma": [ + "HP:0002888" + ], + "thyroid carcinoma": [ + "HP:0002890" + ], + "uterine leiomyosarcoma": [ + "HP:0002891" + ], + "pituitary adenoma": [ + "HP:0002893" + ], + "noncancerous tumor in pituitary gland": [ + "HP:0002893" + ], + "noncancerous tumour in pituitary gland": [ + "HP:0002893" + ], + "neoplasm of the pancreas": [ + "HP:0002894" + ], + "cancer of the pancreas": [ + "HP:0002894" + ], + "increase risk of pancreatic cancer": [ + "HP:0002894" + ], + "increased risk of pancreatic cancer": [ + "HP:0002894" + ], + "neoplasia of the pancreas": [ + "HP:0002894" + ], + "pancreatic cancer": [ + "HP:0002894" + ], + "pancreatic tumor": [ + "HP:0002894" + ], + "pancreatic tumour": [ + "HP:0002894" + ], + "papillary thyroid carcinoma": [ + "HP:0002895" + ], + "papillary carcinoma of thyroid": [ + "HP:0002895" + ], + "thyroid papillary carcinoma": [ + "HP:0002895" + ], + "neoplasm of the liver": [ + "HP:0002896" + ], + "liver cancer": [ + "HP:0002896" + ], + "liver tumor": [ + "HP:0002896" + ], + "liver tumour": [ + "HP:0002896" + ], + "parathyroid adenoma": [ + "HP:0002897" + ], + "parathyroid adenomas": [ + "HP:0002897" + ], + "embryonal neoplasm": [ + "HP:0002898" + ], + "embryonal neoplasia": [ + "HP:0002898" + ], + "embryonal tumor": [ + "HP:0002898" + ], + "embryonal tumors": [ + "HP:0002898" + ], + "embryonal tumour": [ + "HP:0002898" + ], + "embryonal tumours": [ + "HP:0002898" + ], + "hypokalemia": [ + "HP:0002900" + ], + "low blood potassium level": [ + "HP:0002900" + ], + "low blood potassium levels": [ + "HP:0002900" + ], + 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"generalize aminoaciduria": [ + "HP:0002909" + ], + "generalized aminoaciduria": [ + "HP:0002909" + ], + "generalise aminoaciduria": [ + "HP:0002909" + ], + "generalised aminoaciduria": [ + "HP:0002909" + ], + "generalise nonspecific aminoaciduria": [ + "HP:0002909" + ], + "generalised nonspecific aminoaciduria": [ + "HP:0002909" + ], + "generalize nonspecific aminoaciduria": [ + "HP:0002909" + ], + "generalized nonspecific aminoaciduria": [ + "HP:0002909" + ], + "elevate hepatic transaminase": [ + "HP:0002910" + ], + "elevated hepatic transaminase": [ + "HP:0002910" + ], + "abnormal liver enzyme": [ + "HP:0002910" + ], + "abnormal liver enzymes": [ + "HP:0002910" + ], + "abnormal liver function": [ + "HP:0002910" + ], + "abnormal liver function test": [ + "HP:0002910" + ], + "abnormal liver function tests": [ + "HP:0002910" + ], + "elevate liver enzyme": [ + "HP:0002910" + ], + "elevated liver enzymes": [ + "HP:0002910" + ], + "elevate liver function test": [ + "HP:0002910" + ], + "elevated liver function tests": [ + "HP:0002910" + ], + "elevate serum transaminase": [ + "HP:0002910" + ], + "elevated serum transaminases": [ + "HP:0002910" + ], + "elevate transaminase": [ + "HP:0002910" + ], + "elevated transaminases": [ + "HP:0002910" + ], + "high liver enzyme": [ + "HP:0002910" + ], + "high liver enzymes": [ + "HP:0002910" + ], + "increase liver enzyme": [ + "HP:0002910" + ], + "increased liver enzymes": [ + "HP:0002910" + ], + "increase liver function test": [ + "HP:0002910" + ], + "increased liver function tests": [ + "HP:0002910" + ], + "increase transaminase": [ + "HP:0002910" + ], + "increased transaminases": [ + "HP:0002910" + ], + "raise liver enzyme": [ + "HP:0002910" + ], + "raised liver enzymes": [ + "HP:0002910" + ], + "subclinical abnormal liver function test": [ + "HP:0002910" + ], + "subclinical abnormal liver function tests": [ + "HP:0002910" + ], + "methylmalonic acidemia": [ + "HP:0002912" + ], + "elevate circulate methylmalonic acid concentration": [ + "HP:0002912" + ], + "elevated circulating methylmalonic acid concentration": [ + "HP:0002912" + ], + "myoglobinuria": [ + "HP:0002913" + ], + "hyperchloriduria": [ + "HP:0002914" + ], + "increase urinary chloride": [ + "HP:0002914" + ], + "increased urinary chloride": [ + "HP:0002914" + ], + "abnormality of chromosome segregation": [ + "HP:0002916" + ], + "hypomagnesemia": [ + "HP:0002917" + ], + "low blood magnesium level": [ + "HP:0002917" + ], + "low blood magnesium levels": [ + "HP:0002917" + ], + "low blood mg level": [ + "HP:0002917" + ], + "low blood mg levels": [ + "HP:0002917" + ], + "hypermagnesemia": [ + "HP:0002918" + ], + "high blood magnesium level": [ + "HP:0002918" + ], + "high blood magnesium levels": [ + "HP:0002918" + ], + "high blood mg level": [ + "HP:0002918" + ], + "high blood mg levels": [ + "HP:0002918" + ], + "ketonuria": [ + "HP:0002919" + ], + "acetonuria": [ + "HP:0002919" + ], + "ketoaciduria": [ + "HP:0002919" + ], + "ketonaciduria": [ + "HP:0002919" + ], + "ketone body in urine": [ + "HP:0002919" + ], + "ketone bodies in urine": [ + "HP:0002919" + ], + "decrease circulate acth level": [ + "HP:0002920" + ], + "decreased circulating acth level": [ + "HP:0002920" + ], + "abnormality of the cerebrospinal fluid": [ + "HP:0002921" + ], + "abnormal csf finding": [ + "HP:0002921" + ], + "abnormal csf findings": [ + "HP:0002921" + ], + "abnormality of the csf": [ + "HP:0002921" + ], + "increase csf protein": [ + "HP:0002922" + ], + "increased csf protein": [ + "HP:0002922" + ], + "cerebrospinal fluid protein increase": [ + "HP:0002922" + ], + "cerebrospinal fluid protein increased": [ + "HP:0002922" + ], + "cerebrospinal fluid with increased protein": [ + "HP:0002922" + ], + "elevate cerebrospinal fluid protein": [ + "HP:0002922" + ], + "elevated cerebrospinal fluid protein": [ + "HP:0002922" + ], + "elevate csf protein": [ + "HP:0002922" + ], + "elevated csf protein": [ + "HP:0002922" + ], + "hyperproteinorrhachia": [ + "HP:0002922" + ], + "increase protein in csf": [ + "HP:0002922" + ], + "increased protein in csf": [ + "HP:0002922" + ], + "spinal fluid protein elevate": [ + "HP:0002922" + ], + "spinal fluid protein elevated": [ + "HP:0002922" + ], + "rheumatoid factor positive": [ + "HP:0002923" + ], + "obsolete decrease circulate aldosterone level": [ + "HP:0002924" + ], + "obsolete decreased circulating aldosterone level": [ + "HP:0002924" + ], + "elevate circulate thyroid - stimulate hormone concentration": [ + "HP:0002925" + ], + "elevated circulating thyroid - stimulating hormone concentration": [ + "HP:0002925" + ], + "elevate thyroid stimulate hormone": [ + "HP:0002925" + ], + "elevated thyroid stimulating hormone": [ + "HP:0002925" + ], + "elevate thyroid stimulate hormone level": [ + "HP:0002925" + ], + "elevated thyroid stimulating hormone levels": [ + "HP:0002925" + ], + "high tsh": [ + "HP:0002925" + ], + "increase serum thyroid - stimulating hormone": [ + "HP:0002925" + ], + "increased serum thyroid - stimulating hormone": [ + "HP:0002925" + ], + "increase thyroid - stimulate hormone": [ + "HP:0002925" + ], + "increased thyroid - stimulating hormone": [ + "HP:0002925" + ], + "increase thyroid - stimulate hormone level": [ + "HP:0002925" + ], + "increased thyroid - stimulating hormone level": [ + "HP:0002925" + ], + "increase thyrotropin level": [ + "HP:0002925" + ], + "increased thyrotropin level": [ + "HP:0002925" + ], + "thyroid - stimulate hormone excess": [ + "HP:0002925" + ], + "thyroid - stimulating hormone excess": [ + "HP:0002925" + ], + "tsh excess": [ + "HP:0002925" + ], + "abnormality of thyroid physiology": [ + "HP:0002926" + ], + "abnormal thyroid function": [ + "HP:0002926" + ], + "histidinuria": [ + "HP:0002927" + ], + "elevate histidine in urine": [ + "HP:0002927" + ], + "elevated histidine in urine": [ + "HP:0002927" + ], + "high urine histidine level": [ + "HP:0002927" + ], + "high urine histidine levels": [ + "HP:0002927" + ], + "decreased activity of the pyruvate dehydrogenase complex": [ + "HP:0002928" + ], + "decreased activity of the pdh complex": [ + "HP:0002928" + ], + "pyruvate dehydrogenase complex deficiency": [ + "HP:0002928" + ], + "leydig cell insensitivity to gonadotropin": [ + "HP:0002929" + ], + "impaired sensitivity to thyroid hormone": [ + "HP:0002930" + ], + "elevate serum level of free thyroid hormone with nonsuppressed tsh": [ + "HP:0002930" + ], + "elevated serum levels of free thyroid hormone with nonsuppressed tsh": [ + "HP:0002930" + ], + "end - organ unresponsiveness to thyroid hormone": [ + "HP:0002930" + ], + "resistance to thyroid hormone": [ + "HP:0002930" + ], + "thyroid hormone receptor defect": [ + "HP:0002930" + ], + "thyroid hormone resistance": [ + "HP:0002930" + ], + "aldehyde oxidase deficiency": [ + "HP:0002932" + ], + "ventral hernia": [ + "HP:0002933" + ], + "distal sensory impairment": [ + "HP:0002936" + ], + "decrease distal sensation": [ + "HP:0002936" + ], + "decreased distal sensation": [ + "HP:0002936" + ], + "decrease sensation in extremity": [ + "HP:0002936" + ], + "decreased sensation in extremities": [ + "HP:0002936" + ], + "distal sensation loss": [ + "HP:0002936" + ], + "distal sensory impairment in low limb": [ + "HP:0002936" + ], + "distal sensory impairment in lower limbs": [ + "HP:0002936" + ], + "distal sensory impairment of the low extremity": [ + "HP:0002936" + ], + "distal sensory impairment of the lower extremities": [ + "HP:0002936" + ], + "distal sensory loss": [ + "HP:0002936" + ], + "distal sensory loss , upper and low limb": [ + "HP:0002936" + ], + "distal sensory loss , upper and lower limbs": [ + "HP:0002936" + ], + "loss of distal sensation": [ + "HP:0002936" + ], + "hemivertebrae": [ + "HP:0002937" + ], + "hemi - vertebra": [ + "HP:0002937" + ], + "hemi - vertebrae": [ + "HP:0002937" + ], + "hemivertebra": [ + "HP:0002937" + ], + "miss part of vertebra": [ + "HP:0002937" + ], + "missing part of vertebrae": [ + "HP:0002937" + ], + "lumbar hyperlordosis": [ + "HP:0002938" + ], + "exaggerated lumbar lordosis": [ + "HP:0002938" + ], + "excessive inward curvature of low spine": [ + "HP:0002938" + ], + "excessive inward curvature of lower spine": [ + "HP:0002938" + ], + "increase lumbar lordosis": [ + "HP:0002938" + ], + "increased lumbar lordosis": [ + "HP:0002938" + ], + "lumbar lordosis": [ + "HP:0002938" + ], + "prominent lumbar lordosis": [ + "HP:0002938" + ], + "thoracic kyphosis": [ + "HP:0002942" + ], + "accentuate thoracic kyphosis": [ + "HP:0002942" + ], + "accentuated thoracic kyphosis": [ + "HP:0002942" + ], + "exaggerated thoracic kyphosis": [ + "HP:0002942" + ], + "thoracic scoliosis": [ + "HP:0002943" + ], + "thoracolumbar scoliosis": [ + "HP:0002944" + ], + "scoliosis , thoracolumbar": [ + "HP:0002944" + ], + "intervertebral space narrowing": [ + "HP:0002945" + ], + "narrow intervertebral disc space": [ + "HP:0002945" + ], + "narrow intervertebral disc spaces": [ + "HP:0002945" + ], + "narrow intervertebral space": [ + "HP:0002945" + ], + "narrow intervertebral spaces": [ + "HP:0002945" + ], + "supernumerary vertebra": [ + "HP:0002946" + ], + "supernumerary vertebrae": [ + "HP:0002946" + ], + "cervical kyphosis": [ + "HP:0002947" + ], + "round neck": [ + "HP:0002947" + ], + "rounded neck": [ + "HP:0002947" + ], + "vertebral fusion": [ + "HP:0002948" + ], + "fuse vertebra": [ + "HP:0002948" + ], + "fused vertebrae": [ + "HP:0002948" + ], + "fusion of vertebral body": [ + "HP:0002948" + ], + "fusion of vertebral bodies": [ + "HP:0002948" + ], + "spinal fusion": [ + "HP:0002948" + ], + "vertebral body fusion": [ + "HP:0002948" + ], + "fused cervical vertebra": [ + "HP:0002949" + ], + "fused cervical vertebrae": [ + "HP:0002949" + ], + "cervical spine fusion": [ + "HP:0002949" + ], + "cervical vertebral fusion": [ + "HP:0002949" + ], + "fuse neck": [ + "HP:0002949" + ], + "fused neck": [ + "HP:0002949" + ], + "fusion of cervical vertebra": [ + "HP:0002949" + ], + "fusion of cervical vertebrae": [ + "HP:0002949" + ], + "partial absence of cerebellar vermis": [ + "HP:0002951" + ], + "vertebral compression fracture": [ + "HP:0002953" + ], + "compression fracture of a vertebral body": [ + "HP:0002953" + ], + "fracture of vertebral body": [ + "HP:0002953" + ], + "fractures of vertebral bodies": [ + "HP:0002953" + ], + "vertebral body compression": [ + "HP:0002953" + ], + "vertebral collapse": [ + "HP:0002953" + ], + "vertebral compression": [ + "HP:0002953" + ], + "vertebral compression fractures": [ + "HP:0002953" + ], + "vertebral compression or collapse": [ + "HP:0002953" + ], + "granulomatosis": [ + "HP:0002955" + ], + "immune dysregulation": [ + "HP:0002958" + ], + "unregulated immune response": [ + "HP:0002958" + ], + "impaired ig class switch recombination": [ + "HP:0002959" + ], + "impaired b - lymphocyte isotype switching": [ + "HP:0002959" + ], + "autoimmunity": [ + "HP:0002960" + ], + "autoimmune condition": [ + "HP:0002960" + ], + "autoimmune disease": [ + "HP:0002960" + ], + "autoimmune disorder": [ + "HP:0002960" + ], + "dysgammaglobulinemia": [ + "HP:0002961" + ], + "abnormal delay hypersensitivity skin test": [ + "HP:0002963" + ], + "abnormal delayed hypersensitivity skin test": [ + "HP:0002963" + ], + "cutaneous anergy": [ + "HP:0002965" + ], + "absence of delayed hypersensitivity skin test": [ + "HP:0002965" + ], + "lack of delayed skin hypersensitivity reaction": [ + "HP:0002965" + ], + "cubitus valgus": [ + "HP:0002967" + ], + "outward turn elbow": [ + "HP:0002967" + ], + "outward turned elbows": [ + "HP:0002967" + ], + "genu varum": [ + "HP:0002970" + ], + "genu vara": [ + "HP:0002970" + ], + "genua vara": [ + "HP:0002970" + ], + "outward bow - leggedness": [ + "HP:0002970" + ], + "outward bow at knee": [ + "HP:0002970" + ], + "outward bowing at knees": [ + "HP:0002970" + ], + "absent microvilli on the surface of peripheral blood lymphocyte": [ + "HP:0002971" + ], + "absent microvilli on the surface of peripheral blood lymphocytes": [ + "HP:0002971" + ], + "reduce delayed hypersensitivity": [ + "HP:0002972" + ], + "reduced delayed hypersensitivity": [ + "HP:0002972" + ], + "decrease reactivity to skin test antigen": [ + "HP:0002972" + ], + "decreased reactivity to skin test antigens": [ + "HP:0002972" + ], + "deficiency of delayed skin hypersensitivity": [ + "HP:0002972" + ], + "impaired delay hypersensitivity": [ + "HP:0002972" + ], + "impaired delayed hypersensitivity": [ + "HP:0002972" + ], + "abnormality of the forearm": [ + "HP:0002973" + ], + "radioulnar synostosis": [ + "HP:0002974" + ], + "fuse forearm bone": [ + "HP:0002974" + ], + "fused forearm bones": [ + "HP:0002974" + ], + "aplasia / hypoplasia involve the central nervous system": [ + "HP:0002977" + ], + "aplasia / hypoplasia involving the central nervous system": [ + "HP:0002977" + ], + "absent / underdeveloped central nervous system tissue": [ + "HP:0002977" + ], + "aplasia / hypoplasia involve the cns": [ + "HP:0002977" + ], + "aplasia / hypoplasia involving the cns": [ + "HP:0002977" + ], + "bowing of the leg": [ + "HP:0002979" + ], + "bowing of the legs": [ + "HP:0002979" + ], + "bow leg": [ + "HP:0002979" + ], + "bow legs": [ + "HP:0002979" + ], + "bow - leggedness": [ + "HP:0002979" + ], + "bowed legs": [ + "HP:0002979" + ], + "bow low limb": [ + "HP:0002979" + ], + "bowed lower limbs": [ + "HP:0002979" + ], + "femoral bowing": [ + "HP:0002980" + ], + "bow femur": [ + "HP:0002980" + ], + "bowed femur": [ + "HP:0002980" + ], + "bow femura": [ + "HP:0002980" + ], + "bowed femura": [ + "HP:0002980" + ], + "bowed femurs": [ + "HP:0002980" + ], + "bow thighbone": [ + "HP:0002980" + ], + "bowed thighbone": [ + "HP:0002980" + ], + "abnormality of the calf": [ + "HP:0002981" + ], + "tibial bowing": [ + "HP:0002982" + ], + "bow shankbone": [ + "HP:0002982" + ], + "bowed shankbone": [ + "HP:0002982" + ], + "bow shinbone": [ + "HP:0002982" + ], + "bowed shinbone": [ + "HP:0002982" + ], + "bow tibia": [ + "HP:0002982" + ], + "bowed tibia": [ + "HP:0002982" + ], + "bowing of the tibia": [ + "HP:0002982" + ], + "micromelia": [ + "HP:0002983" + ], + "small or short than typical limb": [ + "HP:0002983" + ], + "smaller or shorter than typical limbs": [ + "HP:0002983" + ], + "hypoplasia of the radius": [ + "HP:0002984" + ], + "hypoplastic radius": [ + "HP:0002984" + ], + "hypoplastic radii": [ + "HP:0002984" + ], + "radial hypoplasia": [ + "HP:0002984" + ], + "radial ray hypoplasia": [ + "HP:0002984" + ], + "short radius": [ + "HP:0002984" + ], + "short radii": [ + "HP:0002984" + ], + "shortening of radius": [ + "HP:0002984" + ], + "underdeveloped out large forearm bone": [ + "HP:0002984" + ], + "underdeveloped outer large forearm bone": [ + "HP:0002984" + ], + "radial bowing": [ + "HP:0002986" + ], + "bow radius": [ + "HP:0002986" + ], + "bowed radii": [ + "HP:0002986" + ], + "bowed radius": [ + "HP:0002986" + ], + "bowing of out large bone of the forearm": [ + "HP:0002986" + ], + "bowing of outer large bone of the forearm": [ + "HP:0002986" + ], + "bowing of radius bone of the forearm": [ + "HP:0002986" + ], + "elbow flexion contracture": [ + "HP:0002987" + ], + "contracture of elbow joint": [ + "HP:0002987" + ], + "contracture of elbow": [ + "HP:0002987" + ], + "contractures of elbows": [ + "HP:0002987" + ], + "contracture of the elbow": [ + "HP:0002987" + ], + "contractures of the elbows": [ + "HP:0002987" + ], + "elbow contracture": [ + "HP:0002987" + ], + "elbow contractures": [ + "HP:0002987" + ], + "elbow flexion contractures": [ + "HP:0002987" + ], + "elbow flexion deformity": [ + "HP:0002987" + ], + "fix flexion at the elbow joint": [ + "HP:0002987" + ], + "fixed flexion at the elbow joint": [ + "HP:0002987" + ], + "fibular aplasia": [ + "HP:0002990" + ], + "absent calf bone": [ + "HP:0002990" + ], + "absent fibula": [ + "HP:0002990" + ], + "absent fibulae": [ + "HP:0002990" + ], + "absent - hypoplastic fibula": [ + "HP:0002990" + ], + "absent - hypoplastic fibulae": [ + "HP:0002990" + ], + "abnormality of fibula morphology": [ + "HP:0002991" + ], + "abnormality of the calf bone": [ + "HP:0002991" + ], + "abnormality of tibia morphology": [ + "HP:0002992" + ], + "abnormality of the shankbone": [ + "HP:0002992" + ], + "abnormality of the shinbone": [ + "HP:0002992" + ], + "limited elbow movement": [ + "HP:0002996" + ], + "decrease elbow mobility": [ + "HP:0002996" + ], + "decreased elbow mobility": [ + "HP:0002996" + ], + "limited elbow mobility": [ + "HP:0002996" + ], + "restrict elbow motion": [ + "HP:0002996" + ], + "restricted elbow motion": [ + "HP:0002996" + ], + "abnormality of the ulna": [ + "HP:0002997" + ], + "patellar dislocation": [ + "HP:0002999" + ], + "dislocate kneecap": [ + "HP:0002999" + ], + "dislocated kneecap": [ + "HP:0002999" + ], + "dislocate patella": [ + "HP:0002999" + ], + "dislocated patellae": [ + "HP:0002999" + ], + "dislocation of patella": [ + "HP:0002999" + ], + "glomus jugular tumor": [ + "HP:0003001" + ], + "glomus jugular tumour": [ + "HP:0003001" + ], + "glomus jugulare tumor": [ + "HP:0003001" + ], + "glomus jugulare tumors": [ + "HP:0003001" + ], + "glomus jugulare tumour": [ + "HP:0003001" + ], + "glomus jugulare tumours": [ + "HP:0003001" + ], + "breast carcinoma": [ + "HP:0003002" + ], + "breast cancer": [ + "HP:0003002" + ], + "colon cancer": [ + "HP:0003003" + ], + "ganglioneuroma": [ + "HP:0003005" + ], + "neuroblastoma": [ + "HP:0003006" + ], + "cancer of early nerve cell": [ + "HP:0003006" + ], + "cancer of early nerve cells": [ + "HP:0003006" + ], + "enhanced neurotoxicity of vincristine": [ + "HP:0003009" + ], + "prolong bleeding time": [ + "HP:0003010" + ], + "prolonged bleeding time": [ + "HP:0003010" + ], + "increase bleeding time": [ + "HP:0003010" + ], + "increased bleeding time": [ + "HP:0003010" + ], + "abnormality of the musculature": [ + "HP:0003011" + ], + "muscular abnormality": [ + "HP:0003011" + ], + "bulging epiphysis": [ + "HP:0003013" + ], + "bulging epiphyses": [ + "HP:0003013" + ], + "bulge end part of bone": [ + "HP:0003013" + ], + "bulging end part of bone": [ + "HP:0003013" + ], + "flare metaphysis": [ + "HP:0003015" + ], + "flared metaphysis": [ + "HP:0003015" + ], + "flare wide portion of long bone": [ + "HP:0003015" + ], + "flared wide portion of long bone": [ + "HP:0003015" + ], + "flare , widen metaphyses": [ + "HP:0003015" + ], + "flared , widened metaphyses": [ + "HP:0003015" + ], + "mark metaphyseal flaring of long bone": [ + "HP:0003015" + ], + "marked metaphyseal flaring of long bones": [ + "HP:0003015" + ], + "metaphyseal flaring": [ + "HP:0003015" + ], + "metaphyseal flaring of long bone": [ + "HP:0003015" + ], + "metaphyseal flaring of long bones": [ + "HP:0003015" + ], + "metaphyseal splay": [ + "HP:0003015" + ], + "metaphyseal splaying": [ + "HP:0003015" + ], + "metaphyses flare": [ + "HP:0003015" + ], + "metaphyses flared": [ + "HP:0003015" + ], + "splay metaphyses": [ + "HP:0003015" + ], + "splayed metaphyses": [ + "HP:0003015" + ], + "metaphyseal widening": [ + "HP:0003016" + ], + "broad wide portion of long bone": [ + "HP:0003016" + ], + "wide metaphyses": [ + "HP:0003016" + ], + "widen long bone metaphyses": [ + "HP:0003016" + ], + "widened long bone metaphyses": [ + "HP:0003016" + ], + "widen metaphyses": [ + "HP:0003016" + ], + "widened metaphyses": [ + "HP:0003016" + ], + "abnormality of the wrist": [ + "HP:0003019" + ], + "abnormalities of the wrists": [ + "HP:0003019" + ], + "enlargement of the wrist": [ + "HP:0003020" + ], + "enlargement of the wrists": [ + "HP:0003020" + ], + "metaphyseal cup": [ + "HP:0003021" + ], + "metaphyseal cupping": [ + "HP:0003021" + ], + "hypoplasia of the ulna": [ + "HP:0003022" + ], + "hypoplastic ulna": [ + "HP:0003022" + ], + "short ulna": [ + "HP:0003022" + ], + "short ulnae": [ + "HP:0003022" + ], + "ulnar hypoplasia": [ + "HP:0003022" + ], + "underdeveloped inner large forearm bone": [ + "HP:0003022" + ], + "underdeveloped ulna": [ + "HP:0003022" + ], + "bowing of limb due to multiple fracture": [ + "HP:0003023" + ], + "bowing of limbs due to multiple fractures": [ + "HP:0003023" + ], + "bow limb due to multiple fracture": [ + "HP:0003023" + ], + "bowed limbs due to multiple fractures": [ + "HP:0003023" + ], + "metaphyseal irregularity": [ + "HP:0003025" + ], + "fray , irregular metaphyses": [ + "HP:0003025" + ], + "frayed , irregular metaphyses": [ + "HP:0003025" + ], + "fray , irregular , metaphyses": [ + "HP:0003025" + ], + "frayed , irregular , metaphyses": [ + "HP:0003025" + ], + "irregular metaphyses": [ + "HP:0003025" + ], + "irregular wide portion of a long bone": [ + "HP:0003025" + ], + "metaphyseal fraying": [ + "HP:0003025" + ], + "metaphyseal irregularities": [ + "HP:0003025" + ], + "short long bone": [ + "HP:0003026" + ], + "long bone shortening": [ + "HP:0003026" + ], + "short tubular bone": [ + "HP:0003026" + ], + "short tubular bones": [ + "HP:0003026" + ], + "shorten long tubular bone": [ + "HP:0003026" + ], + "shortened long tubular bones": [ + "HP:0003026" + ], + "mesomelia": [ + "HP:0003027" + ], + "disproportionately short middle portion of limb": [ + "HP:0003027" + ], + "mesomelic limb shorten": [ + "HP:0003027" + ], + "mesomelic limb shortening": [ + "HP:0003027" + ], + "mesomelic shortening of limb": [ + "HP:0003027" + ], + "mesomelic shortening of limbs": [ + "HP:0003027" + ], + "symmetric mesomelic limb shortness": [ + "HP:0003027" + ], + "abnormality of the ankle": [ + "HP:0003028" + ], + "abnormality of the ankles": [ + "HP:0003028" + ], + "enlargement of the ankle": [ + "HP:0003029" + ], + "enlargement of the ankles": [ + "HP:0003029" + ], + "ulnar bowing": [ + "HP:0003031" + ], + "bow ulna": [ + "HP:0003031" + ], + "bowed ulna": [ + "HP:0003031" + ], + "curve ulna": [ + "HP:0003031" + ], + "curved ulna": [ + "HP:0003031" + ], + "curving of inner forearm bone": [ + "HP:0003031" + ], + "diaphyseal sclerosis": [ + "HP:0003034" + ], + "craniodiaphyseal osteosclerosis": [ + "HP:0003034" + ], + "diaphyseal osteosclerosis": [ + "HP:0003034" + ], + "increase bone density in shaft of long bone": [ + "HP:0003034" + ], + "increased bone density in shaft of long bone": [ + "HP:0003034" + ], + "enlarged joint": [ + "HP:0003037" + ], + "enlarged joints": [ + "HP:0003037" + ], + "prominent joint": [ + "HP:0003037" + ], + "prominent joints": [ + "HP:0003037" + ], + "fibular hypoplasia": [ + "HP:0003038" + ], + "hypoplastic fibula": [ + "HP:0003038" + ], + "short calf bone": [ + "HP:0003038" + ], + "short fibula": [ + "HP:0003038" + ], + "short fibulae": [ + "HP:0003038" + ], + "arthropathy": [ + "HP:0003040" + ], + "disease of the joint": [ + "HP:0003040" + ], + "disease of the joints": [ + "HP:0003040" + ], + "humeroradial synostosis": [ + "HP:0003041" + ], + "fusion of upper and low arm bone": [ + "HP:0003041" + ], + "fusion of upper and lower arm bones": [ + "HP:0003041" + ], + "humeral radial synostosis": [ + "HP:0003041" + ], + "humeral - radial synostosis": [ + "HP:0003041" + ], + "radiohumeral synostosis of elbow": [ + "HP:0003041" + ], + "synostosis of radius and humerus": [ + "HP:0003041" + ], + "elbow dislocation": [ + "HP:0003042" + ], + "dislocation of the elbow": [ + "HP:0003042" + ], + "dislocations of the elbows": [ + "HP:0003042" + ], + "elbow dislocations": [ + "HP:0003042" + ], + "radiocapitellar dislocation": [ + "HP:0003042" + ], + "radiohumeral dislocation": [ + "HP:0003042" + ], + "ulnohumeral dislocation": [ + "HP:0003042" + ], + "abnormal shoulder morphology": [ + "HP:0003043" + ], + "abnormality of the shoulder": [ + "HP:0003043" + ], + "shoulder flexion contracture": [ + "HP:0003044" + ], + "abnormal patella morphology": [ + "HP:0003045" + ], + "abnormal kneecap": [ + "HP:0003045" + ], + "abnormality of the patella": [ + "HP:0003045" + ], + "patellar abnormality": [ + "HP:0003045" + ], + "radial head subluxation": [ + "HP:0003048" + ], + "radial subluxation": [ + "HP:0003048" + ], + "radial - head subluxation": [ + "HP:0003048" + ], + "ulnar deviation of the wrist": [ + "HP:0003049" + ], + "ulnar deviation of wrist": [ + "HP:0003049" + ], + "ulnar deviation of wrists": [ + "HP:0003049" + ], + "enlarge metaphyses": [ + "HP:0003051" + ], + "enlarged metaphyses": [ + "HP:0003051" + ], + "enlarge wide portion of a long bone": [ + "HP:0003051" + ], + "enlarged wide portion of a long bone": [ + "HP:0003051" + ], + "epiphyseal deformity of tubular bone": [ + "HP:0003053" + ], + "epiphyseal deformities of tubular bones": [ + "HP:0003053" + ], + "tetraamelia": [ + "HP:0003057" + ], + "tetra - amelia": [ + "HP:0003057" + ], + "abnormality of the radioulnar joint": [ + "HP:0003059" + ], + "abnormality of the radioulnar joints": [ + "HP:0003059" + ], + "abnormality of the humerus": [ + "HP:0003063" + ], + "abnormality of the humeri": [ + "HP:0003063" + ], + "patellar hypoplasia": [ + "HP:0003065" + ], + "hypoplastic patella": [ + "HP:0003065" + ], + "hypoplastic patellae": [ + "HP:0003065" + ], + "small kneecap": [ + "HP:0003065" + ], + "small patella": [ + "HP:0003065" + ], + "small patellae": [ + "HP:0003065" + ], + "underdeveloped kneecap": [ + "HP:0003065" + ], + "limited knee extension": [ + "HP:0003066" + ], + "madelung deformity": [ + "HP:0003067" + ], + "madelung wrist deformity": [ + "HP:0003067" + ], + "madelung - like forearm deformity": [ + "HP:0003068" + ], + "madelung - like forearm deformities": [ + "HP:0003068" + ], + "elbow ankylosis": [ + "HP:0003070" + ], + "flatten epiphysis": [ + "HP:0003071" + ], + "flattened epiphysis": [ + "HP:0003071" + ], + "flat end part of bone": [ + "HP:0003071" + ], + "flat epiphysis": [ + "HP:0003071" + ], + "flat epiphyses": [ + "HP:0003071" + ], + "hypercalcemia": [ + "HP:0003072" + ], + "high blood calcium level": [ + "HP:0003072" + ], + "high blood calcium levels": [ + "HP:0003072" + ], + "hypercalcaemia": [ + "HP:0003072" + ], + "increased calcium in blood": [ + "HP:0003072" + ], + "hypoalbuminemia": [ + "HP:0003073" + ], + "hypoalbuminaemia": [ + "HP:0003073" + ], + "low albumin": [ + "HP:0003073" + ], + "low blood albumin": [ + "HP:0003073" + ], + "hyperglycemia": [ + "HP:0003074" + ], + "high blood glucose": [ + "HP:0003074" + ], + "high blood sugar": [ + "HP:0003074" + ], + "hypoproteinemia": [ + "HP:0003075" + ], + "decrease protein level in blood": [ + "HP:0003075" + ], + "decreased protein levels in blood": [ + "HP:0003075" + ], + "glycosuria": [ + "HP:0003076" + ], + "glucose in urine": [ + "HP:0003076" + ], + "glucosuria": [ + "HP:0003076" + ], + "hyperlipidemia": [ + "HP:0003077" + ], + "elevated lipid in blood": [ + "HP:0003077" + ], + "elevated lipids in blood": [ + "HP:0003077" + ], + "defective dna repair after ultraviolet radiation damage": [ + "HP:0003079" + ], + "hydroxyprolinuria": [ + "HP:0003080" + ], + "elevate urinary hydroxyproline": [ + "HP:0003080" + ], + "elevated urinary hydroxyproline": [ + "HP:0003080" + ], + "increase urinary potassium": [ + "HP:0003081" + ], + "increased urinary potassium": [ + "HP:0003081" + ], + "hyperkaliuresis": [ + "HP:0003081" + ], + "increase urinary k": [ + "HP:0003081" + ], + "increased urinary k": [ + "HP:0003081" + ], + "dislocate radial head": [ + "HP:0003083" + ], + "dislocated radial head": [ + "HP:0003083" + ], + "congenital radial head dislocation": [ + "HP:0003083" + ], + "dislocated radial heads": [ + "HP:0003083" + ], + "dislocate radius": [ + "HP:0003083" + ], + "dislocated radius": [ + "HP:0003083" + ], + "dislocation of radial head": [ + "HP:0003083" + ], + "dislocation of the radial head": [ + "HP:0003083" + ], + "radial dislocation": [ + "HP:0003083" + ], + "radial head dislocation": [ + "HP:0003083" + ], + "radial head dislocation / subluxation": [ + "HP:0003083" + ], + "fracture of the long bone": [ + "HP:0003084" + ], + "fractures of the long bones": [ + "HP:0003084" + ], + "increase long bone fracture rate": [ + "HP:0003084" + ], + "increased long bone fracture rate": [ + "HP:0003084" + ], + "long fibula": [ + "HP:0003085" + ], + "disproportionately long fibula": [ + "HP:0003085" + ], + "long calf bone": [ + "HP:0003085" + ], + "acromesomelia": [ + "HP:0003086" + ], + "premature osteoarthritis": [ + "HP:0003088" + ], + "premature arthritis": [ + "HP:0003088" + ], + "hamstring contracture": [ + "HP:0003089" + ], + "hamstring contractures": [ + "HP:0003089" + ], + "hypoplasia of the capital femoral epiphysis": [ + "HP:0003090" + ], + "small capital femoral epiphysis": [ + "HP:0003090" + ], + "small capital femoral epiphyses": [ + "HP:0003090" + ], + "small femoral capital epiphysis": [ + "HP:0003090" + ], + "small femoral capital epiphyses": [ + "HP:0003090" + ], + "small innermost thighbone end part": [ + "HP:0003090" + ], + "small proximal femoral epiphysis": [ + "HP:0003090" + ], + "small proximal femoral epiphyses": [ + "HP:0003090" + ], + "underdevelopment of the innermost thighbone end part": [ + "HP:0003090" + ], + "trophic limb change": [ + "HP:0003091" + ], + "trophic limb changes": [ + "HP:0003091" + ], + "limited hip extension": [ + "HP:0003093" + ], + "restrict hip extension": [ + "HP:0003093" + ], + "restricted hip extension": [ + "HP:0003093" + ], + "septic arthritis": [ + "HP:0003095" + ], + "infect joint": [ + "HP:0003095" + ], + "infected joint": [ + "HP:0003095" + ], + "short femur": [ + "HP:0003097" + ], + "femoral hypoplasia": [ + "HP:0003097" + ], + "hypoplasia of the femur": [ + "HP:0003097" + ], + "hypoplasia of the femora": [ + "HP:0003097" + ], + "short femurs": [ + "HP:0003097" + ], + "short thighbone": [ + "HP:0003097" + ], + "fibular overgrowth": [ + "HP:0003099" + ], + "overgrowth of calf bone": [ + "HP:0003099" + ], + "slender long bone": [ + "HP:0003100" + ], + "gracile long bone": [ + "HP:0003100" + ], + "gracile long bones": [ + "HP:0003100" + ], + "long bone slender": [ + "HP:0003100" + ], + "long bones slender": [ + "HP:0003100" + ], + "slender long bones": [ + "HP:0003100" + ], + "slender , gracile long tubular bone": [ + "HP:0003100" + ], + "slender , gracile long tubular bones": [ + "HP:0003100" + ], + "thin gracile long bone": [ + "HP:0003100" + ], + "thin gracile long bones": [ + "HP:0003100" + ], + "thin long bone": [ + "HP:0003100" + ], + "thin long bones": [ + "HP:0003100" + ], + "thin , gracile long bone": [ + "HP:0003100" + ], + "thin , gracile long bones": [ + "HP:0003100" + ], + "increase carry angle": [ + "HP:0003102" + ], + "increased carrying angle": [ + "HP:0003102" + ], + "abnormal cortical bone morphology": [ + "HP:0003103" + ], + "abnormal compact bone morphology": [ + "HP:0003103" + ], + "abnormality of cortical bone": [ + "HP:0003103" + ], + "protuberance at end of long bone": [ + "HP:0003105" + ], + "protuberances at ends of long bones": [ + "HP:0003105" + ], + "subperiosteal bone resorption": [ + "HP:0003106" + ], + "subperiosteal erosion": [ + "HP:0003106" + ], + "subperiosteal erosions": [ + "HP:0003106" + ], + "abnormal circulate cholesterol concentration": [ + "HP:0003107" + ], + "abnormal circulating cholesterol concentration": [ + "HP:0003107" + ], + "abnormal cholesterol homeostasis": [ + "HP:0003107" + ], + "abnormality of cholesterol metabolism": [ + "HP:0003107" + ], + "hyperglycinuria": [ + "HP:0003108" + ], + "glycinuria": [ + "HP:0003108" + ], + "high urine glycine level": [ + "HP:0003108" + ], + "high urine glycine levels": [ + "HP:0003108" + ], + "hyperphosphaturia": [ + "HP:0003109" + ], + "high urine phosphate level": [ + "HP:0003109" + ], + "high urine phosphate levels": [ + "HP:0003109" + ], + "phosphaturia": [ + "HP:0003109" + ], + "abnormality of urine homeostasis": [ + "HP:0003110" + ], + "pee issue": [ + "HP:0003110" + ], + "pee issues": [ + "HP:0003110" + ], + "urine issue": [ + "HP:0003110" + ], + "urine issues": [ + "HP:0003110" + ], + "abnormal blood ion concentration": [ + "HP:0003111" + ], + "abnormality of ion homeostasis": [ + "HP:0003111" + ], + "electrolyte disorder": [ + "HP:0003111" + ], + "electrolyte disorders": [ + "HP:0003111" + ], + "electrolyte disturbance": [ + "HP:0003111" + ], + "abnormal circulate amino acid concentration": [ + "HP:0003112" + ], + "abnormal circulating amino acid concentration": [ + "HP:0003112" + ], + "abnormality of serum amino acid level": [ + "HP:0003112" + ], + "abnormality of serum amino acid levels": [ + "HP:0003112" + ], + "hypochloremia": [ + "HP:0003113" + ], + "low blood chloride level": [ + "HP:0003113" + ], + "low blood chloride levels": [ + "HP:0003113" + ], + "obsolete abnormal cardiological finding": [ + "HP:0003114" + ], + "obsolete abnormal cardiological findings": [ + "HP:0003114" + ], + "abnormal ekg": [ + "HP:0003115" + ], + "abnormal ecg": [ + "HP:0003115" + ], + "abnormal electrocardiogram": [ + "HP:0003115" + ], + "ekg abnormality": [ + "HP:0003115" + ], + "abnormal echocardiogram": [ + "HP:0003116" + ], + "abnormal echocardiography": [ + "HP:0003116" + ], + "abnormal circulate hormone concentration": [ + "HP:0003117" + ], + "abnormal circulating hormone concentration": [ + "HP:0003117" + ], + "abnormal circulate hormone level": [ + "HP:0003117" + ], + "abnormal circulating hormone level": [ + "HP:0003117" + ], + "abnormality of circulate hormone level": [ + "HP:0003117" + ], + "abnormality of circulating hormone level": [ + "HP:0003117" + ], + "increase circulate cortisol level": [ + "HP:0003118" + ], + "increased circulating cortisol level": [ + "HP:0003118" + ], + "cushing syndrome": [ + "HP:0003118" + ], + "hypercortisolism": [ + "HP:0003118" + ], + "increase cortisol production": [ + "HP:0003118" + ], + "increased cortisol production": [ + "HP:0003118" + ], + "abnormal circulate lipid concentration": [ + "HP:0003119" + ], + "abnormal circulating lipid concentration": [ + "HP:0003119" + ], + "dyslipidaemia": [ + "HP:0003119" + ], + "dyslipidemia": [ + "HP:0003119" + ], + "limb joint contracture": [ + "HP:0003121" + ], + "limb contracture": [ + "HP:0003121" + ], + "limb contractures": [ + "HP:0003121" + ], + "hypercholesterolemia": [ + "HP:0003124" + ], + "elevate serum cholesterol": [ + "HP:0003124" + ], + "elevated serum cholesterol": [ + "HP:0003124" + ], + "elevate total cholesterol": [ + "HP:0003124" + ], + "elevated total cholesterol": [ + "HP:0003124" + ], + "high cholesterol": [ + "HP:0003124" + ], + "increase total cholesterol": [ + "HP:0003124" + ], + "increased total cholesterol": [ + "HP:0003124" + ], + "reduce factor viii activity": [ + "HP:0003125" + ], + "reduced factor viii activity": [ + "HP:0003125" + ], + "factor viii deficiency": [ + "HP:0003125" + ], + "low - molecular - weight proteinuria": [ + "HP:0003126" + ], + "tubular proteinuria": [ + "HP:0003126" + ], + "hypocalciuria": [ + "HP:0003127" + ], + "low urine calcium level": [ + "HP:0003127" + ], + "low urine calcium levels": [ + "HP:0003127" + ], + "lactic acidosis": [ + "HP:0003128" + ], + "hyperlacticacidemia": [ + "HP:0003128" + ], + "increase lactate in body": [ + "HP:0003128" + ], + "increased lactate in body": [ + "HP:0003128" + ], + "lactic acidemia": [ + "HP:0003128" + ], + "lacticacidemia": [ + "HP:0003128" + ], + "lacticacidosis": [ + "HP:0003128" + ], + "abnormal peripheral myelination": [ + "HP:0003130" + ], + "cystinuria": [ + "HP:0003131" + ], + "high urine cystine level": [ + "HP:0003131" + ], + "high urine cystine levels": [ + "HP:0003131" + ], + "abnormality of the spinocerebellar tract": [ + "HP:0003133" + ], + "abnormality of the spinocerebellar tracts": [ + "HP:0003133" + ], + "abnormality of peripheral nerve conduction": [ + "HP:0003134" + ], + "abnormal peripheral nerve transmission": [ + "HP:0003134" + ], + "sensory and motor nerve conduction abnormality": [ + "HP:0003134" + ], + "sensory and motor nerve conduction abnormalities": [ + "HP:0003134" + ], + "prolinuria": [ + "HP:0003137" + ], + "increase blood urea nitrogen": [ + "HP:0003138" + ], + "increased blood urea nitrogen": [ + "HP:0003138" + ], + "increase bun": [ + "HP:0003138" + ], + "increased bun": [ + "HP:0003138" + ], + "panhypogammaglobulinemia": [ + "HP:0003139" + ], + "panypogammaglobulinemia": [ + "HP:0003139" + ], + "t - wave inversion in the right precordial lead": [ + "HP:0003140" + ], + "t - wave inversion in the right precordial leads": [ + "HP:0003140" + ], + "increase ldl cholesterol concentration": [ + "HP:0003141" + ], + "increased ldl cholesterol concentration": [ + "HP:0003141" + ], + "hyperbetalipoproteinemia": [ + "HP:0003141" + ], + "increase beta - lipoprotein": [ + "HP:0003141" + ], + "increased beta - lipoproteins": [ + "HP:0003141" + ], + "increase circulate ldl level": [ + "HP:0003141" + ], + "increased circulating ldl level": [ + "HP:0003141" + ], + "increase circulate low - density lipoprotein cholesterol": [ + "HP:0003141" + ], + "increased circulating low - density lipoprotein cholesterol": [ + "HP:0003141" + ], + "increase circulate low - density lipoprotein level": [ + "HP:0003141" + ], + "increased circulating low - density lipoprotein levels": [ + "HP:0003141" + ], + "increase ldl cholesterol": [ + "HP:0003141" + ], + "increased ldl cholesterol": [ + "HP:0003141" + ], + "increase ldlc concentration": [ + "HP:0003141" + ], + "increased ldlc concentration": [ + "HP:0003141" + ], + "increase plasma ldl level": [ + "HP:0003141" + ], + "increased plasma ldl levels": [ + "HP:0003141" + ], + "excessive purine production": [ + "HP:0003142" + ], + "increase serum serotonin": [ + "HP:0003144" + ], + "increased serum serotonin": [ + "HP:0003144" + ], + "decrease adenosylcobalamin": [ + "HP:0003145" + ], + "decreased adenosylcobalamin": [ + "HP:0003145" + ], + "decrease adocbl": [ + "HP:0003145" + ], + "decreased adocbl": [ + "HP:0003145" + ], + "hypocholesterolemia": [ + "HP:0003146" + ], + "decrease circulate cholesterol level": [ + "HP:0003146" + ], + "decreased circulating cholesterol level": [ + "HP:0003146" + ], + "elevate serum acid phosphatase": [ + "HP:0003148" + ], + "elevated serum acid phosphatase": [ + "HP:0003148" + ], + "acid phosphatase elevate": [ + "HP:0003148" + ], + "acid phosphatase elevated": [ + "HP:0003148" + ], + "hyperuricosuria": [ + "HP:0003149" + ], + "high urine uric acid level": [ + "HP:0003149" + ], + "glutaric aciduria": [ + "HP:0003150" + ], + "glutarate aciduria": [ + "HP:0003150" + ], + "glutaricaciduria": [ + "HP:0003150" + ], + "increase glutarate level in urine": [ + "HP:0003150" + ], + "increased glutarate level in urine": [ + "HP:0003150" + ], + "obsolete increase serum 1,25 - dihydroxyvitamin d3": [ + "HP:0003152" + ], + "obsolete increased serum 1,25 - dihydroxyvitamin d3": [ + "HP:0003152" + ], + "cystathioninuria": [ + "HP:0003153" + ], + "high urine cystathionine level": [ + "HP:0003153" + ], + "high urine cystathionine levels": [ + "HP:0003153" + ], + "increase circulate acth level": [ + "HP:0003154" + ], + "increased circulating acth level": [ + "HP:0003154" + ], + "high blood corticotropin level": [ + "HP:0003154" + ], + "high blood corticotropin levels": [ + "HP:0003154" + ], + "increase plasma acth": [ + "HP:0003154" + ], + "increased plasma acth": [ + "HP:0003154" + ], + "elevate circulate alkaline phosphatase concentration": [ + "HP:0003155" + ], + "elevated circulating alkaline phosphatase concentration": [ + "HP:0003155" + ], + "elevate alkaline phosphatase": [ + "HP:0003155" + ], + "elevated alkaline phosphatase": [ + "HP:0003155" + ], + "elevate alp": [ + "HP:0003155" + ], + "elevated alp": [ + "HP:0003155" + ], + "greatly elevate alkaline phosphatase": [ + "HP:0003155" + ], + "greatly elevated alkaline phosphatase": [ + "HP:0003155" + ], + "high serum alkaline phosphatase": [ + "HP:0003155" + ], + "hyperphosphatasemia": [ + "HP:0003155" + ], + "hyperphosphatasia": [ + "HP:0003155" + ], + "increase alkaline phosphatase": [ + "HP:0003155" + ], + "increased alkaline phosphatase": [ + "HP:0003155" + ], + "increase serum alkaline phosphatase": [ + "HP:0003155" + ], + "increased serum alkaline phosphatase": [ + "HP:0003155" + ], + "hyposthenuria": [ + "HP:0003158" + ], + "reduce urinary osmolality": [ + "HP:0003158" + ], + "reduced urinary osmolality": [ + "HP:0003158" + ], + "hyperoxaluria": [ + "HP:0003159" + ], + "high urine oxalate level": [ + "HP:0003159" + ], + "high urine oxalate levels": [ + "HP:0003159" + ], + "increase level of oxalate in urine": [ + "HP:0003159" + ], + "increased level of oxalate in urine": [ + "HP:0003159" + ], + "abnormal isoelectric focusing of serum transferrin": [ + "HP:0003160" + ], + "abnormal transferrin isoelectric focusing": [ + "HP:0003160" + ], + "4 - hydroxyphenylpyruvic aciduria": [ + "HP:0003161" + ], + "hydroxyphenylpyruvic aciduria": [ + "HP:0003161" + ], + "fast hypoglycemia": [ + "HP:0003162" + ], + "fasting hypoglycemia": [ + "HP:0003162" + ], + "low blood sugar when fasting": [ + "HP:0003162" + ], + "elevate urinary delta - aminolevulinic acid": [ + "HP:0003163" + ], + "elevated urinary delta - aminolevulinic acid": [ + "HP:0003163" + ], + "hypothalamic gonadotropin - release hormone deficiency": [ + "HP:0003164" + ], + "hypothalamic gonadotropin - releasing hormone deficiency": [ + "HP:0003164" + ], + "hypothalamic gnrh deficiency": [ + "HP:0003164" + ], + "elevate circulate parathyroid hormone level": [ + "HP:0003165" + ], + "elevated circulating parathyroid hormone level": [ + "HP:0003165" + ], + "elevate circulate pth level": [ + "HP:0003165" + ], + "elevated circulating pth level": [ + "HP:0003165" + ], + "elevate serum parathyroid hormone": [ + "HP:0003165" + ], + "elevated serum parathyroid hormone": [ + "HP:0003165" + ], + "elevate serum parathyroid hormone level": [ + "HP:0003165" + ], + "elevated serum parathyroid hormone level": [ + "HP:0003165" + ], + "elevate serum pth": [ + "HP:0003165" + ], + "elevated serum pth": [ + "HP:0003165" + ], + "increase serum parathyroid hormone": [ + "HP:0003165" + ], + "increased serum parathyroid hormone": [ + "HP:0003165" + ], + "increase urinary taurine": [ + "HP:0003166" + ], + "increased urinary taurine": [ + "HP:0003166" + ], + "carnosinuria": [ + "HP:0003167" + ], + "high urine carnosine level": [ + "HP:0003167" + ], + "high urine carnosine levels": [ + "HP:0003167" + ], + "dibasicaminoaciduria": [ + "HP:0003168" + ], + "abnormal acetabulum morphology": [ + "HP:0003170" + ], + "abnormality of the acetabulum": [ + "HP:0003170" + ], + "abnormality of the hipbone socket": [ + "HP:0003170" + ], + "acetabular abnormality": [ + "HP:0003170" + ], + "abnormality of the pubic bone": [ + "HP:0003172" + ], + "abnormality of the pubic bones": [ + "HP:0003172" + ], + "abnormality of the pubis": [ + "HP:0003172" + ], + "hypoplastic pubic bone": [ + "HP:0003173" + ], + "hypoplastic pubic bones": [ + "HP:0003173" + ], + "hypoplastic pubis": [ + "HP:0003173" + ], + "abnormality of the ischium": [ + "HP:0003174" + ], + "abnormality of the ischial bone": [ + "HP:0003174" + ], + "abnormality of the ischial bones": [ + "HP:0003174" + ], + "anomaly of the ischium": [ + "HP:0003174" + ], + "hypoplastic ischia": [ + "HP:0003175" + ], + "hypoplastic ischial bone": [ + "HP:0003175" + ], + "hypoplastic ischial bones": [ + "HP:0003175" + ], + "hypoplastic ischii": [ + "HP:0003175" + ], + "hypoplastic ischium": [ + "HP:0003175" + ], + "square iliac bone": [ + "HP:0003177" + ], + "squared iliac bones": [ + "HP:0003177" + ], + "square iliac bones": [ + "HP:0003177" + ], + "squaring of iliac bone": [ + "HP:0003177" + ], + "squaring of iliac bones": [ + "HP:0003177" + ], + "protrusio acetabuli": [ + "HP:0003179" + ], + "abnormally indent hip socket": [ + "HP:0003179" + ], + "abnormally indented hip sockets": [ + "HP:0003179" + ], + "protrusio acetabulae": [ + "HP:0003179" + ], + "flat acetabular roof": [ + "HP:0003180" + ], + "flat acetabular roofs": [ + "HP:0003180" + ], + "flatten acetabular roof": [ + "HP:0003180" + ], + "flattened acetabular roof": [ + "HP:0003180" + ], + "horizontal acetabulae": [ + "HP:0003180" + ], + "horizontal acetabular roof": [ + "HP:0003180" + ], + "horizontal acetabular roofs": [ + "HP:0003180" + ], + "shallow acetabular fossa": [ + "HP:0003182" + ], + "shallow acetabular fossae": [ + "HP:0003182" + ], + "shallow acetabulum": [ + "HP:0003182" + ], + "shallow acetabula": [ + "HP:0003182" + ], + "shallow acetabulae": [ + "HP:0003182" + ], + "wide pubic symphysis": [ + "HP:0003183" + ], + "wide symphysis of pubis": [ + "HP:0003183" + ], + "decrease hip abduction": [ + "HP:0003184" + ], + "decreased hip abduction": [ + "HP:0003184" + ], + "limited hip abduction": [ + "HP:0003184" + ], + "short great sciatic notch": [ + "HP:0003185" + ], + "short greater sciatic notch": [ + "HP:0003185" + ], + "short sacroiliac notch": [ + "HP:0003185" + ], + "shorten sacroiliac notch": [ + "HP:0003185" + ], + "shortened sacroiliac notches": [ + "HP:0003185" + ], + "small sacroiliac notch": [ + "HP:0003185" + ], + "inverted nipple": [ + "HP:0003186" + ], + "inverted nipples": [ + "HP:0003186" + ], + "invaginated nipple": [ + "HP:0003186" + ], + "invaginated nipples": [ + "HP:0003186" + ], + "breast hypoplasia": [ + "HP:0003187" + ], + "underdeveloped breast": [ + "HP:0003187" + ], + "underdeveloped breasts": [ + "HP:0003187" + ], + "long nose": [ + "HP:0003189" + ], + "elongate nose": [ + "HP:0003189" + ], + "elongated nose": [ + "HP:0003189" + ], + "increase height of nose": [ + "HP:0003189" + ], + "increased height of nose": [ + "HP:0003189" + ], + "increased length of nose": [ + "HP:0003189" + ], + "increase nasal height": [ + "HP:0003189" + ], + "increased nasal height": [ + "HP:0003189" + ], + "increase nasal length": [ + "HP:0003189" + ], + "increased nasal length": [ + "HP:0003189" + ], + "nasal elongation": [ + "HP:0003189" + ], + "cleft ala nasi": [ + "HP:0003191" + ], + "ala nasi , cleft": [ + "HP:0003191" + ], + "alar cleft": [ + "HP:0003191" + ], + "alar clefts": [ + "HP:0003191" + ], + "cleft nasal ala": [ + "HP:0003191" + ], + "cleft nasal alae": [ + "HP:0003191" + ], + "cleft nostril": [ + "HP:0003191" + ], + "nostril coloboma": [ + "HP:0003191" + ], + "notch nasal ala": [ + "HP:0003191" + ], + "notched nasal alae": [ + "HP:0003191" + ], + "allergic rhinitis": [ + "HP:0003193" + ], + "hay fever": [ + "HP:0003193" + ], + "hayfever": [ + "HP:0003193" + ], + "nasal allergy": [ + "HP:0003193" + ], + "nasal allergies": [ + "HP:0003193" + ], + "short nasal bridge": [ + "HP:0003194" + ], + "decreased length of bridge of nose": [ + "HP:0003194" + ], + "decreased length of nasal bridge": [ + "HP:0003194" + ], + "short bridge of nose": [ + "HP:0003194" + ], + "short nose": [ + "HP:0003196" + ], + "decreased length of nose": [ + "HP:0003196" + ], + "hypoplastic nose": [ + "HP:0003196" + ], + "nasal hypoplasia": [ + "HP:0003196" + ], + "shorten nose": [ + "HP:0003196" + ], + "shortened nose": [ + "HP:0003196" + ], + "small nose": [ + "HP:0003196" + ], + "myopathy": [ + "HP:0003198" + ], + "muscle tissue disease": [ + "HP:0003198" + ], + "myopathic change": [ + "HP:0003198" + ], + "myopathic changes": [ + "HP:0003198" + ], + "decreased muscle mass": [ + "HP:0003199" + ], + "rag - red muscle fiber": [ + "HP:0003200" + ], + "ragged - red muscle fibers": [ + "HP:0003200" + ], + "mitochondrial proliferation in muscle tissue": [ + "HP:0003200" + ], + "rag red muscle fiber": [ + "HP:0003200" + ], + "ragged red muscle fibers": [ + "HP:0003200" + ], + "rag red muscle fibre": [ + "HP:0003200" + ], + "ragged red muscle fibres": [ + "HP:0003200" + ], + "rag - red fiber": [ + "HP:0003200" + ], + "ragged - red fibers": [ + "HP:0003200" + ], + "rag - red fibre": [ + "HP:0003200" + ], + "ragged - red fibres": [ + "HP:0003200" + ], + "rag - red muscle fibre": [ + "HP:0003200" + ], + "ragged - red muscle fibres": [ + "HP:0003200" + ], + "rhabdomyolysis": [ + "HP:0003201" + ], + "breakdown of skeletal muscle": [ + "HP:0003201" + ], + "skeletal muscle atrophy": [ + "HP:0003202" + ], + "amyotrophy": [ + "HP:0003202" + ], + "amyotrophy involve the extremity": [ + "HP:0003202" + ], + "amyotrophy involving the extremities": [ + "HP:0003202" + ], + "muscle atrophy": [ + "HP:0003202" + ], + "muscle atrophy , neurogenic": [ + "HP:0003202" + ], + "muscle degeneration": [ + "HP:0003202" + ], + "muscle hypotrophy": [ + "HP:0003202" + ], + "muscle waste": [ + "HP:0003202" + ], + "muscle wasting": [ + "HP:0003202" + ], + "muscular atrophy": [ + "HP:0003202" + ], + "neurogenic muscle atrophy": [ + "HP:0003202" + ], + "neurogenic muscle atrophy , especially in the low limb": [ + "HP:0003202" + ], + "neurogenic muscle atrophy , especially in the lower limbs": [ + "HP:0003202" + ], + "neurogenic muscular atrophy": [ + "HP:0003202" + ], + "impaired oxidative burst": [ + "HP:0003203" + ], + "negative nbt reduction test": [ + "HP:0003203" + ], + "negative nitroblue tetrazolium reduction test": [ + "HP:0003203" + ], + "intracellular accumulation of autofluorescent lipopigment storage material": [ + "HP:0003204" + ], + "curvilinear intracellular accumulation of autofluorescent lipopigment storage material": [ + "HP:0003205" + ], + "'curvilinear profile ' ultrastructurally": [ + "HP:0003205" + ], + "'curvilinear profiles ' ultrastructurally": [ + "HP:0003205" + ], + "'curvilinear profile ' ultrastructurally in cell": [ + "HP:0003205" + ], + "'curvilinear profiles ' ultrastructurally in cells": [ + "HP:0003205" + ], + "curvilinear profile ultrastructurally": [ + "HP:0003205" + ], + "curvilinear profiles ultrastructurally": [ + "HP:0003205" + ], + "intracellular curvilinear profile on ultrastructural analysis": [ + "HP:0003205" + ], + "intracellular curvilinear profiles on ultrastructural analysis": [ + "HP:0003205" + ], + "decreased activity of nadph oxidase": [ + "HP:0003206" + ], + "arterial calcification": [ + "HP:0003207" + ], + "fingerprint intracellular accumulation of autofluorescent lipopigment storage material": [ + "HP:0003208" + ], + "'fingerprint profile ' ultrastructurally in cell": [ + "HP:0003208" + ], + "'fingerprint profiles ' ultrastructurally in cells": [ + "HP:0003208" + ], + "fingerprint profile ultrastructurally": [ + "HP:0003208" + ], + "fingerprint profiles ultrastructurally": [ + "HP:0003208" + ], + "decrease pyruvate carboxylase activity": [ + "HP:0003209" + ], + "decreased pyruvate carboxylase activity": [ + "HP:0003209" + ], + "decrease methylmalonyl - coa mutase activity": [ + "HP:0003210" + ], + "decreased methylmalonyl - coa mutase activity": [ + "HP:0003210" + ], + "decrease methylmalonyl coa mutase activity": [ + "HP:0003210" + ], + "decreased methylmalonyl coa mutase activity": [ + "HP:0003210" + ], + "increase circulate ige level": [ + "HP:0003212" + ], + "increased circulating ige level": [ + "HP:0003212" + ], + "elevate immunoglobulin e": [ + "HP:0003212" + ], + "elevated immunoglobulin e": [ + "HP:0003212" + ], + "elevate serum ige": [ + "HP:0003212" + ], + "elevated serum ige": [ + "HP:0003212" + ], + "high immunoglobulin e": [ + "HP:0003212" + ], + "deficient excision of uv - induced pyrimidine dimer in dna": [ + "HP:0003213" + ], + "deficient excision of uv - induced pyrimidine dimers in dna": [ + "HP:0003213" + ], + "prolonged g2 phase of cell cycle": [ + "HP:0003214" + ], + "dicarboxylic aciduria": [ + "HP:0003215" + ], + "generalize amyloid deposition": [ + "HP:0003216" + ], + "generalized amyloid deposition": [ + "HP:0003216" + ], + "generalise amyloid deposition": [ + "HP:0003216" + ], + "generalised amyloid deposition": [ + "HP:0003216" + ], + "hyperglutaminemia": [ + "HP:0003217" + ], + "high plasma glutamine": [ + "HP:0003217" + ], + "oroticaciduria": [ + "HP:0003218" + ], + "high urine orotic acid level": [ + "HP:0003218" + ], + "high urine orotic acid levels": [ + "HP:0003218" + ], + "increase urinary orotic acid concentration": [ + "HP:0003218" + ], + "increased urinary orotic acid concentration": [ + "HP:0003218" + ], + "orotic aciduria": [ + "HP:0003218" + ], + "ethylmalonic aciduria": [ + "HP:0003219" + ], + "abnormality of chromosome stability": [ + "HP:0003220" + ], + "chromosomal breakage induce by crosslinking agent": [ + "HP:0003221" + ], + "chromosomal breakage induced by crosslinking agents": [ + "HP:0003221" + ], + "chromosomal breakage induce by diepoxybutane": [ + "HP:0003221" + ], + "chromosomal breakage induced by diepoxybutane": [ + "HP:0003221" + ], + "chromosomal breakage induce by mitomycin c": [ + "HP:0003221" + ], + "chromosomal breakage induced by mitomycin c": [ + "HP:0003221" + ], + "decrease methylcobalamin": [ + "HP:0003223" + ], + "decreased methylcobalamin": [ + "HP:0003223" + ], + "methylcobalamin deficiency": [ + "HP:0003223" + ], + "increase cellular sensitivity to uv light": [ + "HP:0003224" + ], + "increased cellular sensitivity to uv light": [ + "HP:0003224" + ], + "reduce coagulation factor v activity": [ + "HP:0003225" + ], + "reduced coagulation factor v activity": [ + "HP:0003225" + ], + "factor v deficiency": [ + "HP:0003225" + ], + "reduce factor v activity": [ + "HP:0003225" + ], + "reduced factor v activity": [ + "HP:0003225" + ], + "rectilinear intracellular accumulation of autofluorescent lipopigment storage material": [ + "HP:0003226" + ], + "rectilinear profile ultrastructurally": [ + "HP:0003226" + ], + "rectilinear profiles ultrastructurally": [ + "HP:0003226" + ], + "hypernatremia": [ + "HP:0003228" + ], + "high blood sodium level": [ + "HP:0003228" + ], + "high blood sodium levels": [ + "HP:0003228" + ], + "hypertyrosinemia": [ + "HP:0003231" + ], + "increase tyrosine in blood": [ + "HP:0003231" + ], + "increased tyrosine in blood": [ + "HP:0003231" + ], + "tyrosinemia": [ + "HP:0003231" + ], + "mitochondrial malic enzyme reduce": [ + "HP:0003232" + ], + "mitochondrial malic enzyme reduced": [ + "HP:0003232" + ], + "decrease mitochondrial malic enzyme": [ + "HP:0003232" + ], + "decreased mitochondrial malic enzyme": [ + "HP:0003232" + ], + "decrease hdl cholesterol concentration": [ + "HP:0003233" + ], + "decreased hdl cholesterol concentration": [ + "HP:0003233" + ], + "decrease circulate high - density lipoprotein cholesterol": [ + "HP:0003233" + ], + "decreased circulating high - density lipoprotein cholesterol": [ + "HP:0003233" + ], + "decrease circulate high - density lipoprotein level": [ + "HP:0003233" + ], + "decreased circulating high - density lipoprotein levels": [ + "HP:0003233" + ], + "decrease hdl cholesterol": [ + "HP:0003233" + ], + "decreased hdl cholesterol": [ + "HP:0003233" + ], + "hypoalphalipoproteinemia": [ + "HP:0003233" + ], + "low hdl - cholesterol": [ + "HP:0003233" + ], + "decrease plasma carnitine": [ + "HP:0003234" + ], + "decreased plasma carnitine": [ + "HP:0003234" + ], + "carnitine deficiency": [ + "HP:0003234" + ], + "hypermethioninemia": [ + "HP:0003235" + ], + "increase methionine in blood": [ + "HP:0003235" + ], + "increased methionine in blood": [ + "HP:0003235" + ], + "methioninemia": [ + "HP:0003235" + ], + "elevate circulate creatine kinase concentration": [ + "HP:0003236" + ], + "elevated circulating creatine kinase concentration": [ + "HP:0003236" + ], + "elevate blood creatine phosphokinase": [ + "HP:0003236" + ], + "elevated blood creatine phosphokinase": [ + "HP:0003236" + ], + "elevate circulate creatine phosphokinase": [ + "HP:0003236" + ], + "elevated circulating creatine phosphokinase": [ + "HP:0003236" + ], + "elevate creatine kinase": [ + "HP:0003236" + ], + "elevated creatine kinase": [ + "HP:0003236" + ], + "elevate serum cpk": [ + "HP:0003236" + ], + "elevated serum cpk": [ + "HP:0003236" + ], + "elevate serum creatine kinase": [ + "HP:0003236" + ], + "elevated serum creatine kinase": [ + "HP:0003236" + ], + "elevate serum creatine phosphokinase": [ + "HP:0003236" + ], + "elevated serum creatine phosphokinase": [ + "HP:0003236" + ], + "high serum creatine kinase": [ + "HP:0003236" + ], + "increase cpk": [ + "HP:0003236" + ], + "increased cpk": [ + "HP:0003236" + ], + "increase creatine kinase": [ + "HP:0003236" + ], + "increased creatine kinase": [ + "HP:0003236" + ], + "increase creatine phosphokinase": [ + "HP:0003236" + ], + "increased creatine phosphokinase": [ + "HP:0003236" + ], + "increase serum ck": [ + "HP:0003236" + ], + "increased serum ck": [ + "HP:0003236" + ], + "increase serum creatine kinase": [ + "HP:0003236" + ], + "increased serum creatine kinase": [ + "HP:0003236" + ], + "increase serum creatine phosphokinase": [ + "HP:0003236" + ], + "increased serum creatine phosphokinase": [ + "HP:0003236" + ], + "increase circulate igg level": [ + "HP:0003237" + ], + "increased circulating igg level": [ + "HP:0003237" + ], + "increase igg level": [ + "HP:0003237" + ], + "increased igg level": [ + "HP:0003237" + ], + "increased level of igg": [ + "HP:0003237" + ], + "increased levels of igg": [ + "HP:0003237" + ], + "increase total igg in blood": [ + "HP:0003237" + ], + "increased total igg in blood": [ + "HP:0003237" + ], + "hyperpepsinogenemia i": [ + "HP:0003238" + ], + "phosphoethanolaminuria": [ + "HP:0003239" + ], + "high urine phosphoethanolamine level": [ + "HP:0003239" + ], + "high urine phosphoethanolamine levels": [ + "HP:0003239" + ], + "increase phosphoribosylpyrophosphate synthetase level": [ + "HP:0003240" + ], + "increased phosphoribosylpyrophosphate synthetase level": [ + "HP:0003240" + ], + "increase phosphoribosyl pyrophosphate synthetase activity": [ + "HP:0003240" + ], + "increased phosphoribosyl pyrophosphate synthetase activity": [ + "HP:0003240" + ], + "increase prps1 activity": [ + "HP:0003240" + ], + "increased prps1 activity": [ + "HP:0003240" + ], + "external genital hypoplasia": [ + "HP:0003241" + ], + "hypogenitalism": [ + "HP:0003241" + ], + "small genitalia": [ + "HP:0003241" + ], + "underdevelopment of external reproductive organ": [ + "HP:0003241" + ], + "underdevelopment of external reproductive organs": [ + "HP:0003241" + ], + "penile hypospadias": [ + "HP:0003244" + ], + "prominent scrotal raphe": [ + "HP:0003246" + ], + "prominent perineal raphe": [ + "HP:0003246" + ], + "overgrowth of external genitalia": [ + "HP:0003247" + ], + "gonadal tissue inappropriate for external genitalia or chromosomal sex": [ + "HP:0003248" + ], + "genital ulcer": [ + "HP:0003249" + ], + "genital ulcers": [ + "HP:0003249" + ], + "aplasia of the vagina": [ + "HP:0003250" + ], + "absent vagina": [ + "HP:0003250" + ], + "congenital absence of the vagina": [ + "HP:0003250" + ], + "male infertility": [ + "HP:0003251" + ], + "anteriorly displace genitalia": [ + "HP:0003252" + ], + "anteriorly displaced genitalia": [ + "HP:0003252" + ], + "abnormality of dna repair": [ + "HP:0003254" + ], + "abnormality of the coagulation cascade": [ + "HP:0003256" + ], + "coagulopathy": [ + "HP:0003256" + ], + "glyoxalase deficiency": [ + "HP:0003258" + ], + "elevate circulate creatinine concentration": [ + "HP:0003259" + ], + "elevated circulating creatinine concentration": [ + "HP:0003259" + ], + "elevate creatinine": [ + "HP:0003259" + ], + "elevated creatinine": [ + "HP:0003259" + ], + "elevate serum creatinine": [ + "HP:0003259" + ], + "elevated serum creatinine": [ + "HP:0003259" + ], + "high blood creatinine level": [ + "HP:0003259" + ], + "increase creatinine": [ + "HP:0003259" + ], + "increased creatinine": [ + "HP:0003259" + ], + "increase serum creatinine": [ + "HP:0003259" + ], + "increased serum creatinine": [ + "HP:0003259" + ], + "hydroxyprolinemia": [ + "HP:0003260" + ], + "high blood hydroxyproline level": [ + "HP:0003260" + ], + "high blood hydroxyproline levels": [ + "HP:0003260" + ], + "increase circulate iga level": [ + "HP:0003261" + ], + "increased circulating iga level": [ + "HP:0003261" + ], + "elevate iga": [ + "HP:0003261" + ], + "elevated iga": [ + "HP:0003261" + ], + "elevate serum iga": [ + "HP:0003261" + ], + "elevated serum iga": [ + "HP:0003261" + ], + "iga hypergammaglobulinemia": [ + "HP:0003261" + ], + "increased level of iga": [ + "HP:0003261" + ], + "increased levels of iga": [ + "HP:0003261" + ], + "increase serum iga": [ + "HP:0003261" + ], + "increased serum iga": [ + "HP:0003261" + ], + "smooth muscle antibody positivity": [ + "HP:0003262" + ], + "anti - smooth muscle antibody positivity": [ + "HP:0003262" + ], + "smooth muscle antibody positive": [ + "HP:0003262" + ], + "deficiency of n - acetylglucosamine - 1 - phosphotransferase": [ + "HP:0003264" + ], + "neonatal hyperbilirubinemia": [ + "HP:0003265" + ], + "high blood bilirubin level in neonate": [ + "HP:0003265" + ], + "high blood bilirubin levels in neonate": [ + "HP:0003265" + ], + "hyperbilirubinemia , neonatal": [ + "HP:0003265" + ], + "reduce orotidine 5 - prime phosphate decarboxylase level": [ + "HP:0003267" + ], + "reduced orotidine 5 - prime phosphate decarboxylase level": [ + "HP:0003267" + ], + "orotidine - 5 - prime - phosphate decarboxylase defect": [ + "HP:0003267" + ], + "argininuria": [ + "HP:0003268" + ], + "high urine arginine level": [ + "HP:0003268" + ], + "high urine arginine levels": [ + "HP:0003268" + ], + "sudanophilic leukodystrophy": [ + "HP:0003269" + ], + "abdominal distention": [ + "HP:0003270" + ], + "abdominal bloating": [ + "HP:0003270" + ], + "abdominal distension": [ + "HP:0003270" + ], + "abdominal swelling": [ + "HP:0003270" + ], + "belly bloat": [ + "HP:0003270" + ], + "belly bloating": [ + "HP:0003270" + ], + "bloating": [ + "HP:0003270" + ], + "distend abdomen": [ + "HP:0003270" + ], + "distended abdomen": [ + "HP:0003270" + ], + "visceromegaly": [ + "HP:0003271" + ], + "abnormal hip bone morphology": [ + "HP:0003272" + ], + "abnormality of the hip bone": [ + "HP:0003272" + ], + "abnormality of the hip": [ + "HP:0003272" + ], + "abnormality of the hips": [ + "HP:0003272" + ], + "hip contracture": [ + "HP:0003273" + ], + "flexion contracture of hip": [ + "HP:0003273" + ], + "flexion contracture of hips": [ + "HP:0003273" + ], + "flexion contractures of hips": [ + "HP:0003273" + ], + "hip contractures": [ + "HP:0003273" + ], + "hip flexion contracture": [ + "HP:0003273" + ], + "hip flexion contractures": [ + "HP:0003273" + ], + "hypoplastic acetabulae": [ + "HP:0003274" + ], + "acetabular hypoplasia": [ + "HP:0003274" + ], + "hypoplastic acetabulum": [ + "HP:0003274" + ], + "hypoplastic acetabula": [ + "HP:0003274" + ], + "narrow pelvis bone": [ + "HP:0003275" + ], + "narrow pelvis": [ + "HP:0003275" + ], + "pelvic bone exostosis": [ + "HP:0003276" + ], + "pelvic bone exostoses": [ + "HP:0003276" + ], + "pelvic exostosis": [ + "HP:0003276" + ], + "pelvic exostoses": [ + "HP:0003276" + ], + "constrict iliac wing": [ + "HP:0003277" + ], + "constricted iliac wing": [ + "HP:0003277" + ], + "constricted iliac wings": [ + "HP:0003277" + ], + "square pelvis bone": [ + "HP:0003278" + ], + "square pelvis": [ + "HP:0003278" + ], + "square off pelvis": [ + "HP:0003278" + ], + "squared off pelvis": [ + "HP:0003278" + ], + "coxa magna": [ + "HP:0003279" + ], + "increase circulate ferritin concentration": [ + "HP:0003281" + ], + "increased circulating ferritin concentration": [ + "HP:0003281" + ], + "elevate serum ferritin": [ + "HP:0003281" + ], + "elevated serum ferritin": [ + "HP:0003281" + ], + "high ferritin level": [ + "HP:0003281" + ], + "hyperferritinaemia": [ + "HP:0003281" + ], + "hyperferritinemia": [ + "HP:0003281" + ], + "increase ferritin": [ + "HP:0003281" + ], + "increased ferritin": [ + "HP:0003281" + ], + "increase plasma ferritin": [ + "HP:0003281" + ], + "increased plasma ferritin": [ + "HP:0003281" + ], + "increase serum ferritin level": [ + "HP:0003281" + ], + "increased serum ferritin level": [ + "HP:0003281" + ], + "low alkaline phosphatase": [ + "HP:0003282" + ], + "decrease serum alkaline phosphatase": [ + "HP:0003282" + ], + "decreased serum alkaline phosphatase": [ + "HP:0003282" + ], + "low alp": [ + "HP:0003282" + ], + "cystathioninemia": [ + "HP:0003286" + ], + "high blood cystathionine level": [ + "HP:0003286" + ], + "high blood cystathionine levels": [ + "HP:0003286" + ], + "abnormality of mitochondrial metabolism": [ + "HP:0003287" + ], + "mitochondrial dysfunction": [ + "HP:0003287" + ], + "mitochondrial propionyl - coa carboxylase defect": [ + "HP:0003288" + ], + "mitochondrial pcc defect": [ + "HP:0003288" + ], + "decrease serum leptin": [ + "HP:0003292" + ], + "decreased serum leptin": [ + "HP:0003292" + ], + "reduce circulate leptin level": [ + "HP:0003292" + ], + "reduced circulating leptin level": [ + "HP:0003292" + ], + "obsolete impair fsh and lh secretion": [ + "HP:0003295" + ], + "obsolete impaired fsh and lh secretion": [ + "HP:0003295" + ], + "hyperthreoninuria": [ + "HP:0003296" + ], + "high urine threonine level": [ + "HP:0003296" + ], + "high urine threonine levels": [ + "HP:0003296" + ], + "hyperlysinuria": [ + "HP:0003297" + ], + "high urine lysine level": [ + "HP:0003297" + ], + "high urine lysine levels": [ + "HP:0003297" + ], + "lysinuria": [ + "HP:0003297" + ], + "spina bifida occulta": [ + "HP:0003298" + ], + "ovoid vertebral body": [ + "HP:0003300" + ], + "ovoid vertebral bodies": [ + "HP:0003300" + ], + "bullet vertebral body": [ + "HP:0003300" + ], + "oval vertebral body": [ + "HP:0003300" + ], + "oval vertebral bodies": [ + "HP:0003300" + ], + "ovoid vertebra": [ + "HP:0003300" + ], + "ovoid vertebrae": [ + "HP:0003300" + ], + "ovoid - shaped vertebral body": [ + "HP:0003300" + ], + "ovoid - shaped vertebral bodies": [ + "HP:0003300" + ], + "irregular vertebral endplate": [ + "HP:0003301" + ], + "irregular vertebral endplates": [ + "HP:0003301" + ], + "end - plate irregularity": [ + "HP:0003301" + ], + "end - plate irregularities": [ + "HP:0003301" + ], + "endplate irregularity": [ + "HP:0003301" + ], + "endplate irregularities": [ + "HP:0003301" + ], + "irregular end plate": [ + "HP:0003301" + ], + "irregular end plates": [ + "HP:0003301" + ], + "irregular endplate": [ + "HP:0003301" + ], + "irregular endplates": [ + "HP:0003301" + ], + "irregular vertebral plate": [ + "HP:0003301" + ], + "irregular vertebral plates": [ + "HP:0003301" + ], + "vertebral endplate irregularity": [ + "HP:0003301" + ], + "spondylolisthesis": [ + "HP:0003302" + ], + "displacement of one backbone compare to another": [ + "HP:0003302" + ], + "displacement of one backbone compared to another": [ + "HP:0003302" + ], + "slip backbone": [ + "HP:0003302" + ], + "slipped backbone": [ + "HP:0003302" + ], + "spondylolithesis": [ + "HP:0003302" + ], + "spondylolysis": [ + "HP:0003304" + ], + "block vertebra": [ + "HP:0003305" + ], + "block vertebrae": [ + "HP:0003305" + ], + "spinal rigidity": [ + "HP:0003306" + ], + "reduce spine movement": [ + "HP:0003306" + ], + "reduced spine movement": [ + "HP:0003306" + ], + "rigid spine": [ + "HP:0003306" + ], + "hyperlordosis": [ + "HP:0003307" + ], + "lordosis": [ + "HP:0003307" + ], + "prominent swayback": [ + "HP:0003307" + ], + "cervical subluxation": [ + "HP:0003308" + ], + "ovoid thoracolumbar vertebra": [ + "HP:0003309" + ], + "ovoid thoracolumbar vertebrae": [ + "HP:0003309" + ], + "ovoid thoracic and lumbar vertebra": [ + "HP:0003309" + ], + "ovoid thoracic and lumbar vertebrae": [ + "HP:0003309" + ], + "abnormality of the odontoid process": [ + "HP:0003310" + ], + "abnormal odontoid peg": [ + "HP:0003310" + ], + "abnormal odontoid process": [ + "HP:0003310" + ], + "hypoplasia of the odontoid process": [ + "HP:0003311" + ], + "hypoplastic odontoid process": [ + "HP:0003311" + ], + "odontoid hypoplasia": [ + "HP:0003311" + ], + "small odontoid peg": [ + "HP:0003311" + ], + "small odontoid process": [ + "HP:0003311" + ], + "abnormal form of the vertebral body": [ + "HP:0003312" + ], + "abnormal form of the vertebral bodies": [ + "HP:0003312" + ], + "abnormally shape vertebra": [ + "HP:0003312" + ], + "abnormally shaped vertebrae": [ + "HP:0003312" + ], + "butterfly vertebra": [ + "HP:0003316" + ], + "butterfly vertebrae": [ + "HP:0003316" + ], + "anterior rachischisis": [ + "HP:0003316" + ], + "sagittal clefting of vertebra": [ + "HP:0003316" + ], + "sagittal clefting of vertebrae": [ + "HP:0003316" + ], + "cervical spine hypermobility": [ + "HP:0003318" + ], + "cervical spine joint hypermobility": [ + "HP:0003318" + ], + "abnormality of the cervical spine": [ + "HP:0003319" + ], + "abnormal cervical spine": [ + "HP:0003319" + ], + "abnormality of cervical vertebra": [ + "HP:0003319" + ], + "abnormality of the cervical vertebra": [ + "HP:0003319" + ], + "abnormality of the cervical vertebrae": [ + "HP:0003319" + ], + "cervical spine abnormality": [ + "HP:0003319" + ], + "cervical spine abnormalities": [ + "HP:0003319" + ], + "cervical vertebral abnormality": [ + "HP:0003319" + ], + "cervical vertebral abnormalities": [ + "HP:0003319" + ], + "cervical vertebral anomaly": [ + "HP:0003319" + ], + "cervical vertebral anomalies": [ + "HP:0003319" + ], + "disorder of cervical vertebra": [ + "HP:0003319" + ], + "c1 - c2 subluxation": [ + "HP:0003320" + ], + "biconcave flatten vertebra": [ + "HP:0003321" + ], + "biconcave flattened vertebrae": [ + "HP:0003321" + ], + "progressive muscle weakness": [ + "HP:0003323" + ], + "muscle weakness , progressive": [ + "HP:0003323" + ], + "progressive muscular weakness": [ + "HP:0003323" + ], + "generalize muscle weakness": [ + "HP:0003324" + ], + "generalized muscle weakness": [ + "HP:0003324" + ], + "generalise muscle weakness": [ + "HP:0003324" + ], + "generalised muscle weakness": [ + "HP:0003324" + ], + "generalise weakness": [ + "HP:0003324" + ], + "generalised weakness": [ + "HP:0003324" + ], + "generalize weakness": [ + "HP:0003324" + ], + "generalized weakness": [ + "HP:0003324" + ], + "muscle weakness , diffuse": [ + "HP:0003324" + ], + "muscle weakness , generalise": [ + "HP:0003324" + ], + "muscle weakness , generalised": [ + "HP:0003324" + ], + "muscle weakness , generalize": [ + "HP:0003324" + ], + "muscle weakness , generalized": [ + "HP:0003324" + ], + "limb - girdle muscle weakness": [ + "HP:0003325" + ], + "limb girdle weakness": [ + "HP:0003325" + ], + "muscle weakness , limb - girdle": [ + "HP:0003325" + ], + "muscular weakness , limb - girdle": [ + "HP:0003325" + ], + "myalgia": [ + "HP:0003326" + ], + "muscle ache": [ + "HP:0003326" + ], + "muscle pain": [ + "HP:0003326" + ], + "myalgias": [ + "HP:0003326" + ], + "axial muscle weakness": [ + "HP:0003327" + ], + "abnormal hair laboratory examination": [ + "HP:0003328" + ], + "hair shaft flatten at irregular interval and twist through 180 degree about their ax": [ + "HP:0003329" + ], + "hair shafts flattened at irregular intervals and twisted through 180 degrees about their axes": [ + "HP:0003329" + ], + "abnormal bone structure": [ + "HP:0003330" + ], + "absent primary metaphyseal spongiosa": [ + "HP:0003332" + ], + "increase serum beta - hexosaminidase": [ + "HP:0003333" + ], + "increased serum beta - hexosaminidase": [ + "HP:0003333" + ], + "elevate circulate catecholamine level": [ + "HP:0003334" + ], + "elevated circulating catecholamine level": [ + "HP:0003334" + ], + "obsolete low gonadotropin ( secondary hypogonadism )": [ + "HP:0003335" + ], + "obsolete low gonadotropins ( secondary hypogonadism )": [ + "HP:0003335" + ], + "abnormal enchondral ossification": [ + "HP:0003336" + ], + "reduce prothrombin consumption": [ + "HP:0003337" + ], + "reduced prothrombin consumption": [ + "HP:0003337" + ], + "poor prothrombin consumption": [ + "HP:0003337" + ], + "focal necrosis of right ventricular muscle cell": [ + "HP:0003338" + ], + "focal necrosis of right ventricular muscle cells": [ + "HP:0003338" + ], + "pyrimidine - responsive megaloblastic anemia": [ + "HP:0003339" + ], + "anaemia correct by uridylic acid and cytidylic acid": [ + "HP:0003339" + ], + "anaemia corrected by uridylic acid and cytidylic acid": [ + "HP:0003339" + ], + "anemia correct by uridylic acid and cytidylic acid": [ + "HP:0003339" + ], + "anemia corrected by uridylic acid and cytidylic acid": [ + "HP:0003339" + ], + "pyrimidine - responsive megaloblastic anaemia": [ + "HP:0003339" + ], + "obsolete abnormal dermatological laboratory finding": [ + "HP:0003340" + ], + "obsolete abnormal dermatological laboratory findings": [ + "HP:0003340" + ], + "subepidermal blister with cleavage in the lamina lucida": [ + "HP:0003341" + ], + "subepidermal blistering with cleavage in the lamina lucida": [ + "HP:0003341" + ], + "blister with junctional split": [ + "HP:0003341" + ], + "blistering with junctional split": [ + "HP:0003341" + ], + "junctional split": [ + "HP:0003341" + ], + "reduce glutathione synthetase level": [ + "HP:0003343" + ], + "reduced glutathione synthetase level": [ + "HP:0003343" + ], + "glutathione synthetase deficiency": [ + "HP:0003343" + ], + "3 - methylglutaric aciduria": [ + "HP:0003344" + ], + "3 - methylglutaricaciduria": [ + "HP:0003344" + ], + "elevate urinary norepinephrine": [ + "HP:0003345" + ], + "elevated urinary norepinephrine": [ + "HP:0003345" + ], + "impaired lymphocyte transformation with phytohemagglutinin": [ + "HP:0003347" + ], + "hyperalaninemia": [ + "HP:0003348" + ], + "increase blood alanine": [ + "HP:0003348" + ], + "increased blood alanine": [ + "HP:0003348" + ], + "increase serum alanine": [ + "HP:0003348" + ], + "increased serum alanine": [ + "HP:0003348" + ], + "low cholesterol esterification rate": [ + "HP:0003349" + ], + "decrease circulate renin level": [ + "HP:0003351" + ], + "decreased circulating renin level": [ + "HP:0003351" + ], + "decrease plasma renin activity": [ + "HP:0003351" + ], + "decreased plasma renin activity": [ + "HP:0003351" + ], + "low plasma renin activity": [ + "HP:0003351" + ], + "suppress plasma renin activity": [ + "HP:0003351" + ], + "suppressed plasma renin activity": [ + "HP:0003351" + ], + "endopolyploidy on chromosome study of bone marrow": [ + "HP:0003352" + ], + "endopolyploidy on chromosome studies of bone marrow": [ + "HP:0003352" + ], + "propionyl - coa carboxylase deficiency": [ + "HP:0003353" + ], + "hyperthreoninemia": [ + "HP:0003354" + ], + "elevate circulate threonine": [ + "HP:0003354" + ], + "elevated circulating threonine": [ + "HP:0003354" + ], + "high blood threonine level": [ + "HP:0003354" + ], + "high blood threonine levels": [ + "HP:0003354" + ], + "aminoaciduria": [ + "HP:0003355" + ], + "abnormal urinary amino - acid finding": [ + "HP:0003355" + ], + "abnormal urinary amino - acid findings": [ + "HP:0003355" + ], + "high urine amino acid level": [ + "HP:0003355" + ], + "high urine amino acid levels": [ + "HP:0003355" + ], + "hyperaminoaciduria": [ + "HP:0003355" + ], + "increased level of animo acid in urine": [ + "HP:0003355" + ], + "increased levels of animo acids in urine": [ + "HP:0003355" + ], + "thymic hormone decrease": [ + "HP:0003357" + ], + "thymic hormone decreased": [ + "HP:0003357" + ], + "decrease thymic hormone": [ + "HP:0003357" + ], + "decreased thymic hormone": [ + "HP:0003357" + ], + "elevate intracellular cystine": [ + "HP:0003358" + ], + "elevated intracellular cystine": [ + "HP:0003358" + ], + "decrease urinary sulfate": [ + "HP:0003359" + ], + "decreased urinary sulfate": [ + "HP:0003359" + ], + "decrease urinary sulphate": [ + "HP:0003359" + ], + "decreased urinary sulphate": [ + "HP:0003359" + ], + "tryptophanuria": [ + "HP:0003361" + ], + "high urine tryptophan level": [ + "HP:0003361" + ], + "high urine tryptophan levels": [ + "HP:0003361" + ], + "increase vldl cholesterol concentration": [ + "HP:0003362" + ], + "increased vldl cholesterol concentration": [ + "HP:0003362" + ], + "increase circulate very - low - density lipoprotein cholesterol": [ + "HP:0003362" + ], + "increased circulating very - low - density lipoprotein cholesterol": [ + "HP:0003362" + ], + "increase circulate very - low - density lipoprotein level": [ + "HP:0003362" + ], + "increased circulating very - low - density lipoprotein levels": [ + "HP:0003362" + ], + "increase plasma vldl cholesterol": [ + "HP:0003362" + ], + "increased plasma vldl cholesterol": [ + "HP:0003362" + ], + "abdominal situs inversus": [ + "HP:0003363" + ], + "situs inversus visceralis": [ + "HP:0003363" + ], + "situs inversus viscerum": [ + "HP:0003363" + ], + "arthralgia of the hip": [ + "HP:0003365" + ], + "coxalgia": [ + "HP:0003365" + ], + "hip arthralgia": [ + "HP:0003365" + ], + "hip joint pain": [ + "HP:0003365" + ], + "abnormal femoral neck / head morphology": [ + "HP:0003366" + ], + "abnormal neck or head of thigh bone": [ + "HP:0003366" + ], + "abnormality of the femoral neck or head region": [ + "HP:0003366" + ], + "abnormal femoral neck morphology": [ + "HP:0003367" + ], + "abnormal neck of thigh bone": [ + "HP:0003367" + ], + "abnormality of the femoral neck": [ + "HP:0003367" + ], + "abnormal femoral head morphology": [ + "HP:0003368" + ], + "abnormal head of thigh bone": [ + "HP:0003368" + ], + "abnormality of the femoral head": [ + "HP:0003368" + ], + "flat capital femoral epiphysis": [ + "HP:0003370" + ], + "flat capital femoral epiphyses": [ + "HP:0003370" + ], + "flat end part of innermost thighbone": [ + "HP:0003370" + ], + "flat femoral capital epiphysis": [ + "HP:0003370" + ], + "flat femoral capital epiphyses": [ + "HP:0003370" + ], + "flat proximal femoral epiphysis": [ + "HP:0003370" + ], + "flat proximal femoral epiphyses": [ + "HP:0003370" + ], + "flatten proximal femoral epiphysis": [ + "HP:0003370" + ], + "flattened proximal femoral epiphyses": [ + "HP:0003370" + ], + "enlargement of the proximal femoral epiphysis": [ + "HP:0003371" + ], + "enlarge capital femoral epiphysis": [ + "HP:0003371" + ], + "enlarged capital femoral epiphyses": [ + "HP:0003371" + ], + "enlarged end part of innermost thighbone": [ + "HP:0003371" + ], + "narrow great sciatic notch": [ + "HP:0003375" + ], + "narrow greater sciatic notch": [ + "HP:0003375" + ], + "narrow great sacrosciatic notch": [ + "HP:0003375" + ], + "narrow greater sacrosciatic notches": [ + "HP:0003375" + ], + "narrow sacroiliac notch": [ + "HP:0003375" + ], + "narrow sacrosciatic notch": [ + "HP:0003375" + ], + "narrow sciatic notch": [ + "HP:0003375" + ], + "narrow sciatic notches": [ + "HP:0003375" + ], + "narrowed greater sciatic notch": [ + "HP:0003375" + ], + "narrowed sacrosciatic notch": [ + "HP:0003375" + ], + "small sacrosciatic notch": [ + "HP:0003375" + ], + "small sacrosciatic notches": [ + "HP:0003375" + ], + "steppage gait": [ + "HP:0003376" + ], + "'steppage ' gait": [ + "HP:0003376" + ], + "high stepping": [ + "HP:0003376" + ], + "axonal degeneration / regeneration": [ + "HP:0003378" + ], + "axon degeneration and regeneration": [ + "HP:0003378" + ], + "decreased number of peripheral myelinated nerve fiber": [ + "HP:0003380" + ], + "decreased number of peripheral myelinated nerve fibers": [ + "HP:0003380" + ], + "decreased number of large and small myelinated fiber": [ + "HP:0003380" + ], + "decreased number of large and small myelinated fibers": [ + "HP:0003380" + ], + "decreased number of large and small myelinated fibre": [ + "HP:0003380" + ], + "decreased number of large and small myelinated fibres": [ + "HP:0003380" + ], + "decreased number of peripheral myelinated nerve fibre": [ + "HP:0003380" + ], + "decreased number of peripheral myelinated nerve fibres": [ + "HP:0003380" + ], + "loss of myelinated fiber": [ + "HP:0003380" + ], + "loss of myelinated fibers": [ + "HP:0003380" + ], + "loss of myelinated fibre": [ + "HP:0003380" + ], + "loss of myelinated fibres": [ + "HP:0003380" + ], + "hypertrophic nerve change": [ + "HP:0003382" + ], + "hypertrophic nerve changes": [ + "HP:0003382" + ], + "onion bulb formation": [ + "HP:0003383" + ], + "'onion bulb ' formation": [ + "HP:0003383" + ], + "'onion bulb ' formations": [ + "HP:0003383" + ], + "onion bulb formations": [ + "HP:0003383" + ], + "peripheral axonal atrophy": [ + "HP:0003384" + ], + "decreased number of large peripheral myelinated nerve fiber": [ + "HP:0003387" + ], + "decreased number of large peripheral myelinated nerve fibers": [ + "HP:0003387" + ], + "decreased number of large peripheral myelinated nerve fibre": [ + "HP:0003387" + ], + "decreased number of large 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"generalised hypotonia due to defect at the neuromuscular junction": [ + "HP:0003397" + ], + "abnormal synaptic transmission at the neuromuscular junction": [ + "HP:0003398" + ], + "abnormality of neuromuscular transmission": [ + "HP:0003398" + ], + "basal lamina onion bulb formation": [ + "HP:0003400" + ], + "basal lamina 'onion bulb ' formation on nerve biopsy": [ + "HP:0003400" + ], + "basal lamina 'onion bulb ' formations on nerve biopsy": [ + "HP:0003400" + ], + "paresthesia": [ + "HP:0003401" + ], + "paresthesias": [ + "HP:0003401" + ], + "pin and needle feel": [ + "HP:0003401" + ], + "pins and needles feeling": [ + "HP:0003401" + ], + "tingle": [ + "HP:0003401" + ], + "tingling": [ + "HP:0003401" + ], + "decreased miniature endplate potential": [ + "HP:0003402" + ], + "decreased miniature endplate potentials": [ + "HP:0003402" + ], + "decrease mepp": [ + "HP:0003402" + ], + "decreased mepp": [ + "HP:0003402" + ], + "small miniature endplate current": [ + "HP:0003402" + ], + 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urine trimethylamine levels": [ + "HP:0003614" + ], + "premature separation of centromeric heterochromatin": [ + "HP:0003616" + ], + "juvenile onset": [ + "HP:0003621" + ], + "sign and symptom begin before 15 year of age": [ + "HP:0003621" + ], + "signs and symptoms begin before 15 years of age": [ + "HP:0003621" + ], + "neonatal onset": [ + "HP:0003623" + ], + "onset in first week of life": [ + "HP:0003623" + ], + "onset in first weeks of life": [ + "HP:0003623" + ], + "onset in neonatal period": [ + "HP:0003623" + ], + "amyoplasia": [ + "HP:0003634" + ], + "absent muscle since birth": [ + "HP:0003634" + ], + "absent muscles since birth": [ + "HP:0003634" + ], + "congenital absence of muscle": [ + "HP:0003634" + ], + "congenital absence of muscles": [ + "HP:0003634" + ], + "loss of subcutaneous adipose tissue in limb": [ + "HP:0003635" + ], + "loss of subcutaneous adipose tissue in limbs": [ + "HP:0003635" + ], + "loss of fat tissue below the skin in limb": [ + "HP:0003635" + ], + "loss of fat tissue below the skin in limbs": [ + "HP:0003635" + ], + "loss of subcutaneous adipose tissue from extremity": [ + "HP:0003635" + ], + "loss of subcutaneous adipose tissue from extremities": [ + "HP:0003635" + ], + "reduce 4 - hydroxyphenylpyruvate dioxygenase level": [ + "HP:0003637" + ], + "reduced 4 - hydroxyphenylpyruvate dioxygenase level": [ + "HP:0003637" + ], + "reducted hppd activity": [ + "HP:0003637" + ], + "elevate urinary epinephrine": [ + "HP:0003639" + ], + "elevated urinary epinephrine": [ + "HP:0003639" + ], + "increase urinary epinephrine": [ + "HP:0003639" + ], + "increased urinary epinephrine": [ + "HP:0003639" + ], + "cns foam cell": [ + "HP:0003640" + ], + "cns foam cells": [ + "HP:0003640" + ], + "hemoglobinuria": [ + "HP:0003641" + ], + "haemoglobin in urine": [ + "HP:0003641" + ], + "hemoglobin in urine": [ + "HP:0003641" + ], + "type i transferrin isoform profile": [ + "HP:0003642" + ], + "abnormal isoelectric focusing of serum transferrin , type i pattern": [ + "HP:0003642" + ], + "isoelectric focusing of serum transferrin consistent with cdg type i": [ + "HP:0003642" + ], + "type 1 transferrin isoform profile": [ + "HP:0003642" + ], + "sulfite oxidase deficiency": [ + "HP:0003643" + ], + "prolong partial thromboplastin time": [ + "HP:0003645" + ], + "prolonged partial thromboplastin time": [ + "HP:0003645" + ], + "abnormal partial thromboplastin time": [ + "HP:0003645" + ], + "delay thromboplastin generation": [ + "HP:0003645" + ], + "delayed thromboplastin generation": [ + "HP:0003645" + ], + "partial thromboplastin time prolong": [ + "HP:0003645" + ], + "partial thromboplastin time prolonged": [ + "HP:0003645" + ], + "prolong activate partial thromboplastin time": [ + "HP:0003645" + ], + "prolonged activated partial thromboplastin time": [ + "HP:0003645" + ], + "prolong ptt": [ + "HP:0003645" + ], + "prolonged ptt": [ + "HP:0003645" + ], + "bicarbonaturia": [ + "HP:0003646" + ], + "increase urine bicarbonate concentration": 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foam cell": [ + "HP:0003651" + ], + "presence of foam cells": [ + "HP:0003651" + ], + "recurrent myoglobinuria": [ + "HP:0003652" + ], + "myoglobinuria , episodic": [ + "HP:0003652" + ], + "myoglobinuria , recurrent": [ + "HP:0003652" + ], + "cellular metachromasia": [ + "HP:0003653" + ], + "reduce dihydropyrimidine dehydrogenase level": [ + "HP:0003654" + ], + "reduced dihydropyrimidine dehydrogenase level": [ + "HP:0003654" + ], + "dihydropyrimidine dehydrogenase deficiency": [ + "HP:0003654" + ], + "reduce level of n - acetylglucosaminyltransferase ii": [ + "HP:0003655" + ], + "reduced level of n - acetylglucosaminyltransferase ii": [ + "HP:0003655" + ], + "deficient n - acetylglucosaminyltransferase ii": [ + "HP:0003655" + ], + "decrease beta - glucocerebrosidase level": [ + "HP:0003656" + ], + "decreased beta - glucocerebrosidase level": [ + "HP:0003656" + ], + "decrease lysosomal acid glucosylceramidase activity": [ + "HP:0003656" + ], + "decreased lysosomal acid glucosylceramidase activity": [ + "HP:0003656" + ], + "granular osmiophilic deposit ( grod ) in cell": [ + "HP:0003657" + ], + "granular osmiophilic deposits ( grod ) in cells": [ + "HP:0003657" + ], + "hypomethioninemia": [ + "HP:0003658" + ], + "decrease plasma methionine": [ + "HP:0003658" + ], + "decreased plasma methionine": [ + "HP:0003658" + ], + "decrease serum methionine": [ + "HP:0003658" + ], + "decreased serum methionine": [ + "HP:0003658" + ], + "amyotrophy of the musculature of the pelvis": [ + "HP:0003665" + ], + "onset": [ + "HP:0003674" + ], + "age of onset": [ + "HP:0003674" + ], + "age symptom begin": [ + "HP:0003674" + ], + "age symptoms begin": [ + "HP:0003674" + ], + "progressive": [ + "HP:0003676" + ], + "progressive disorder": [ + "HP:0003676" + ], + "worsens with time": [ + "HP:0003676" + ], + "slowly progressive": [ + "HP:0003677" + ], + "sign and symptom worsen slowly with time": [ + "HP:0003677" + ], + "signs and symptoms worsen slowly with time": [ + 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skeletal muscle fibers": [ + "HP:0003687" + ], + "central nucleus": [ + "HP:0003687" + ], + "central nuclei": [ + "HP:0003687" + ], + "centralise nucleus": [ + "HP:0003687" + ], + "centralised nuclei": [ + "HP:0003687" + ], + "centralise sarcomeric nucleus": [ + "HP:0003687" + ], + "centralised sarcomeric nuclei": [ + "HP:0003687" + ], + "centralize nucleus": [ + "HP:0003687" + ], + "centralized nuclei": [ + "HP:0003687" + ], + "centralize sarcomeric nucleus": [ + "HP:0003687" + ], + "centralized sarcomeric nuclei": [ + "HP:0003687" + ], + "centrally nucleated skeletal muscle fibre": [ + "HP:0003687" + ], + "centrally nucleated skeletal muscle fibres": [ + "HP:0003687" + ], + "cytochrome c oxidase - negative muscle fiber": [ + "HP:0003688" + ], + "cytochrome c oxidase - negative muscle fibers": [ + "HP:0003688" + ], + "cytochrome c oxidase deficiency in skeletal muscle": [ + "HP:0003688" + ], + "cytochrome c oxidase - negative muscle fibre": [ + "HP:0003688" + ], + "cytochrome c oxidase - negative muscle fibres": [ + "HP:0003688" + ], + "decreased activity of cytochrome c oxidase in muscle tissue": [ + "HP:0003688" + ], + "decrease skeletal muscle cytochrome c oxidase activity": [ + "HP:0003688" + ], + "decreased skeletal muscle cytochrome c oxidase activity": [ + "HP:0003688" + ], + "multiple mitochondrial dna deletion": [ + "HP:0003689" + ], + "multiple mitochondrial dna deletions": [ + "HP:0003689" + ], + "multiple mtdna deletion": [ + "HP:0003689" + ], + "multiple mtdna deletions": [ + "HP:0003689" + ], + "limb muscle weakness": [ + "HP:0003690" + ], + "limb weakness": [ + "HP:0003690" + ], + "scapular winging": [ + "HP:0003691" + ], + "scapula alata": [ + "HP:0003691" + ], + "scapular weakness": [ + "HP:0003691" + ], + "wing scapula": [ + "HP:0003691" + ], + "winged scapulae": [ + "HP:0003691" + ], + "winged scapulas": [ + "HP:0003691" + ], + "wing shoulder blade": [ + "HP:0003691" + ], + "winged shoulder blade": [ + "HP:0003691" + ], + "distal amyotrophy": [ + "HP:0003693" + ], + "amyotrophy of distal limb muscle": [ + "HP:0003693" + ], + "amyotrophy of distal limb muscles": [ + "HP:0003693" + ], + "distal amyotrophy , especially of the hand and foot": [ + "HP:0003693" + ], + "distal amyotrophy , especially of the hands and feet": [ + "HP:0003693" + ], + "distal limb muscle atrophy": [ + "HP:0003693" + ], + "distal muscle atrophy": [ + "HP:0003693" + ], + "distal muscle atrophy , upper and low limb": [ + "HP:0003693" + ], + "distal muscle atrophy , upper and lower limbs": [ + "HP:0003693" + ], + "distal muscle degeneration": [ + "HP:0003693" + ], + "distal muscle waste": [ + "HP:0003693" + ], + "distal muscle wasting": [ + "HP:0003693" + ], + "distal muscular atrophy": [ + "HP:0003693" + ], + "muscle atrophy , distal": [ + "HP:0003693" + ], + "late - onset proximal muscle weakness": [ + "HP:0003694" + ], + "absent epiphysis of the distal phalanx of the 5th finger": [ + "HP:0003696" + ], + "absent end part of the outermost bone of the little finger": [ + "HP:0003696" + ], + "absent end part of the outermost bone of the pinkie finger": [ + "HP:0003696" + ], + "absent end part of the outermost bone of the pinky finger": [ + "HP:0003696" + ], + "scapuloperoneal amyotrophy": [ + "HP:0003697" + ], + "scapuloperoneal atrophy": [ + "HP:0003697" + ], + "difficulty stand": [ + "HP:0003698" + ], + "difficulty standing": [ + "HP:0003698" + ], + "difficulty in stand": [ + "HP:0003698" + ], + "difficulty in standing": [ + "HP:0003698" + ], + "stand instability": [ + "HP:0003698" + ], + "standing instability": [ + "HP:0003698" + ], + "generalize amyotrophy": [ + "HP:0003700" + ], + "generalized amyotrophy": [ + "HP:0003700" + ], + "diffuse amyotrophy": [ + "HP:0003700" + ], + "diffuse muscle atrophy": [ + "HP:0003700" + ], + "diffuse muscle waste": [ + "HP:0003700" + ], + "diffuse muscle wasting": [ + "HP:0003700" + ], + "diffuse skeletal muscle waste": [ + "HP:0003700" + ], + "diffuse skeletal muscle wasting": [ + 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exercise": [ + "HP:0003710" + ], + "muscle cramps on exercise": [ + "HP:0003710" + ], + "muscle cramp on exertion": [ + "HP:0003710" + ], + "muscle cramps on exertion": [ + "HP:0003710" + ], + "muscle cramp with exertion": [ + "HP:0003710" + ], + "muscle cramps with exertion": [ + "HP:0003710" + ], + "skeletal muscle hypertrophy": [ + "HP:0003712" + ], + "hypertrophic muscle": [ + "HP:0003712" + ], + "hypertrophic muscles": [ + "HP:0003712" + ], + "increase skeletal muscle cell": [ + "HP:0003712" + ], + "increased skeletal muscle cells": [ + "HP:0003712" + ], + "muscle hypertrophy": [ + "HP:0003712" + ], + "muscular hypertrophy": [ + "HP:0003712" + ], + "muscle fiber necrosis": [ + "HP:0003713" + ], + "muscle fibre necrosis": [ + "HP:0003713" + ], + "myofibrillar myopathy": [ + "HP:0003715" + ], + "myofibrillar change": [ + "HP:0003715" + ], + "myofibrillar changes": [ + "HP:0003715" + ], + "generalize muscular appearance from birth": [ + "HP:0003716" + ], + "generalized muscular appearance from birth": [ + "HP:0003716" + ], + "generalise muscular appearance from birth": [ + "HP:0003716" + ], + "generalised muscular appearance from birth": [ + "HP:0003716" + ], + "minimal subcutaneous fat": [ + "HP:0003717" + ], + "minimal fat below the skin": [ + "HP:0003717" + ], + "muscle mounding": [ + "HP:0003719" + ], + "generalize muscle hypertrophy": [ + "HP:0003720" + ], + "generalized muscle hypertrophy": [ + "HP:0003720" + ], + "generalised increase in muscle cell size": [ + "HP:0003720" + ], + "generalised muscle hypertrophy": [ + "HP:0003720" + ], + "generalized increase in muscle cell size": [ + "HP:0003720" + ], + "neck flexor weakness": [ + "HP:0003722" + ], + "neck flexion weakness": [ + "HP:0003722" + ], + "neck flexor muscle weakness": [ + "HP:0003722" + ], + "shoulder girdle muscle atrophy": [ + "HP:0003724" + ], + "shoulder girdle atrophy": [ + "HP:0003724" + ], + "shoulder girdle muscle waste": [ + "HP:0003724" + ], + "shoulder girdle muscle wasting": [ + "HP:0003724" + ], + "shoulder - girdle muscle atrophy": [ + "HP:0003724" + ], + "firm muscle": [ + "HP:0003725" + ], + "firm muscles": [ + "HP:0003725" + ], + "enteroviral dermatomyositis syndrome": [ + "HP:0003729" + ], + "emg : myotonic run": [ + "HP:0003730" + ], + "emg : myotonic runs": [ + "HP:0003730" + ], + "emg : spontaneous , repetitive electrical activity": [ + "HP:0003730" + ], + "quadriceps muscle weakness": [ + "HP:0003731" + ], + "quadriceps weakness": [ + "HP:0003731" + ], + "thigh hypertrophy": [ + "HP:0003733" + ], + "increase thigh size": [ + "HP:0003733" + ], + "increased thigh size": [ + "HP:0003733" + ], + "autophagic vacuole": [ + "HP:0003736" + ], + "autophagic vacuoles": [ + "HP:0003736" + ], + "mitochondrial myopathy": [ + "HP:0003737" + ], + "exercise - induced myalgia": [ + "HP:0003738" + ], + "exercise - induced muscle pain": [ + "HP:0003738" + ], + "muscle pain on exercise": [ + "HP:0003738" + ], + "muscle pain with exercise": [ + "HP:0003738" + ], + "muscle pain , exercise - induced": [ + "HP:0003738" + ], + "myoclonic spasm": [ + "HP:0003739" + ], + "myoclonic spasms": [ + "HP:0003739" + ], + "myotonia with warm - up phenomenon": [ + "HP:0003740" + ], + "congenital muscular dystrophy": [ + "HP:0003741" + ], + "muscular dystrophy , congenital": [ + "HP:0003741" + ], + "genetic anticipation": [ + "HP:0003743" + ], + "genetic anticipation with paternal anticipation bias": [ + "HP:0003744" + ], + "paternal anticipation bias": [ + "HP:0003744" + ], + "sporadic": [ + "HP:0003745" + ], + "isolated case": [ + "HP:0003745" + ], + "isolated cases": [ + "HP:0003745" + ], + "no previous family history": [ + "HP:0003745" + ], + "pelvic girdle muscle weakness": [ + "HP:0003749" + ], + "hip girdle muscle weakness": [ + "HP:0003749" + ], + "hip girdle weakness": [ + "HP:0003749" + ], + "hip - girdle muscle weakness": [ + "HP:0003749" + ], + "pelvic girdle weakness": [ + "HP:0003749" + ], + "increase muscle fatiguability": [ + "HP:0003750" + ], + "increased muscle fatiguability": [ + "HP:0003750" + ], + "muscle fatigue": [ + "HP:0003750" + ], + "episodic flaccid weakness": [ + "HP:0003752" + ], + "type 1 fiber relatively small than type 2 fiber": [ + "HP:0003755" + ], + "type 1 fibers relatively smaller than type 2 fibers": [ + "HP:0003755" + ], + "type 1 fibre relatively small than type 2 fibre": [ + "HP:0003755" + ], + "type 1 fibres relatively smaller than type 2 fibres": [ + "HP:0003755" + ], + "skeletal myopathy": [ + "HP:0003756" + ], + "reduce subcutaneous adipose tissue": [ + "HP:0003758" + ], + "reduced subcutaneous adipose tissue": [ + "HP:0003758" + ], + "decrease subcutaneous adipose tissue": [ + "HP:0003758" + ], + "decreased subcutaneous adipose tissue": [ + "HP:0003758" + ], + "decrease subcutaneous fat": [ + "HP:0003758" + ], + "decreased subcutaneous fat": [ + "HP:0003758" + ], + "reduce fat tissue below the skin": [ + "HP:0003758" + ], + "reduced fat tissue below the skin": [ + "HP:0003758" + ], + "reduce subcutaneous fat": [ + "HP:0003758" + ], + "reduced subcutaneous fat": [ + "HP:0003758" + ], + "scanty adipose tissue": [ + "HP:0003758" + ], + "hypoplasia of lymphatic vessel": [ + "HP:0003759" + ], + "hypoplasia of lymphatic vessels": [ + "HP:0003759" + ], + "underdeveloped lymphatic vessel": [ + "HP:0003759" + ], + "underdeveloped lymphatic vessels": [ + "HP:0003759" + ], + "percussion - induced rapid roll muscle contraction": [ + "HP:0003760" + ], + "percussion - induced rapid rolling muscle contractions": [ + "HP:0003760" + ], + "calcinosis": [ + "HP:0003761" + ], + "calcium buildup in soft tissue of body": [ + "HP:0003761" + ], + "calcium buildup in soft tissues of body": [ + "HP:0003761" + ], + "uterus didelphys": [ + "HP:0003762" + ], + "double uterus": [ + "HP:0003762" + ], + "bruxism": [ + "HP:0003763" + ], + "teeth grind": [ + "HP:0003763" + ], + "teeth grinding": [ + "HP:0003763" + ], + "nevus": [ + "HP:0003764" + ], + "mole": [ + "HP:0003764" + ], + "naevi": [ + "HP:0003764" + ], + "naevus": [ + "HP:0003764" + ], + "nevi": [ + "HP:0003764" + ], + "psoriasiform dermatitis": [ + "HP:0003765" + ], + "psoriasis": [ + "HP:0003765" + ], + "periodic paralysis": [ + "HP:0003768" + ], + "episodic paralysis": [ + "HP:0003768" + ], + "pulp calcification": [ + "HP:0003771" + ], + "false denticle": [ + "HP:0003771" + ], + "false denticles": [ + "HP:0003771" + ], + "false pulp stone": [ + "HP:0003771" + ], + "false pulp stones": [ + "HP:0003771" + ], + "pulp calcifications": [ + "HP:0003771" + ], + "pulp denticle": [ + "HP:0003771" + ], + "pulp denticles": [ + "HP:0003771" + ], + "pulp stone": [ + "HP:0003771" + ], + "pulp stones": [ + "HP:0003771" + ], + "pulpoliths": [ + "HP:0003771" + ], + "true denticle": [ + "HP:0003771" + ], + "true denticles": [ + "HP:0003771" + ], + "true pulp stone": [ + "HP:0003771" + ], + "true pulp stones": [ + "HP:0003771" + ], + "stage 5 chronic kidney disease": [ + "HP:0003774" + ], + "chronic renal failure": [ + "HP:0003774" + ], + "end stage renal disease": [ + "HP:0003774" + ], + "end stage renal failure": [ + "HP:0003774" + ], + "end - stage renal disease": [ + "HP:0003774" + ], + "end - stage renal failure": [ + "HP:0003774" + ], + "renal failure , endstage": [ + "HP:0003774" + ], + "pili torti": [ + "HP:0003777" + ], + "flatten and twist hair": [ + "HP:0003777" + ], + "flattened and twisted hair": [ + "HP:0003777" + ], + "short mandibular ramus": [ + "HP:0003778" + ], + "short mandibular rami": [ + "HP:0003778" + ], + "decreased height of mandibular ramus": [ + "HP:0003778" + ], + "decreased size of mandibular ramus": [ + "HP:0003778" + ], + "short body and ramus of mandible": [ + "HP:0003778" + ], + "underdeveloped mandibular ramus": [ + "HP:0003778" + ], + "underdeveloped mandibular rami": [ + "HP:0003778" + ], + "antegonial notching of mandible": [ + "HP:0003779" + ], + "deep antegonial notch of mandible": [ + "HP:0003779" + ], + "large antegonial notch of mandible": [ + "HP:0003779" + ], + "excessive salivation": [ + "HP:0003781" + ], + "excessive production of saliva": [ + "HP:0003781" + ], + "hypersalivation": [ + "HP:0003781" + ], + "mouth watering": [ + "HP:0003781" + ], + "oversalivation": [ + "HP:0003781" + ], + "ptyalism": [ + "HP:0003781" + ], + "watery mouth": [ + "HP:0003781" + ], + "eunuchoid habitus": [ + "HP:0003782" + ], + "externally rotate / abduct leg": [ + "HP:0003783" + ], + "externally rotated / abducted legs": [ + "HP:0003783" + ], + "type 1 collagen overmodification": [ + "HP:0003784" + ], + "decrease csf homovanillic acid": [ + "HP:0003785" + ], + "decreased csf homovanillic acid": [ + "HP:0003785" + ], + "type 1 and type 2 muscle fiber minicore region": [ + "HP:0003787" + ], + "type 1 and type 2 muscle fiber minicore regions": [ + "HP:0003787" + ], + "type 1 and type 2 muscle fibre minicore region": [ + "HP:0003787" + ], + "type 1 and type 2 muscle fibre minicore regions": [ + "HP:0003787" + ], + "minicore myopathy": [ + "HP:0003789" + ], + "deposit immunoreactive to beta - amyloid protein": [ + "HP:0003791" + ], + "deposits immunoreactive to beta - amyloid protein": [ + "HP:0003791" + ], + "short middle phalanx of toe": [ + "HP:0003795" + ], + "short middle bone ( foot )": [ + "HP:0003795" + ], + "short middle bones ( feet )": [ + "HP:0003795" + ], + "short middle phalanges of toes": [ + "HP:0003795" + ], + "irregular iliac crest": [ + "HP:0003796" + ], + "limb - girdle muscle atrophy": [ + "HP:0003797" + ], + "limb - girdle myopathy": [ + "HP:0003797" + ], + "wasting of limb - girdle muscle": [ + "HP:0003797" + ], + "nemaline body": [ + "HP:0003798" + ], + "nemaline bodies": [ + "HP:0003798" + ], + "nemaline rod": [ + "HP:0003798" + ], + "nemaline rods": [ + "HP:0003798" + ], + "mark delay in bone age": [ + "HP:0003799" + ], + "marked delay in bone age": [ + "HP:0003799" + ], + "mark retardation in skeletal maturation": [ + "HP:0003799" + ], + "marked retardation in skeletal maturation": [ + "HP:0003799" + ], + "markedly retard bone age": [ + "HP:0003799" + ], + "markedly retarded bone age": [ + "HP:0003799" + ], + "muscle abnormality relate to mitochondrial dysfunction": [ + "HP:0003800" + ], + "muscle abnormality related to mitochondrial dysfunction": [ + "HP:0003800" + ], + "type 1 muscle fiber predominance": [ + "HP:0003803" + ], + "type 1 muscle fibre predominance": [ + "HP:0003803" + ], + "type i muscle fiber predominance": [ + "HP:0003803" + ], + "type i muscle fibre predominance": [ + "HP:0003803" + ], + "rim vacuole": [ + "HP:0003805" + ], + "rimmed vacuoles": [ + "HP:0003805" + ], + "'rimmed vacuole ' on biopsy": [ + "HP:0003805" + ], + "'rimmed vacuoles ' on biopsy": [ + "HP:0003805" + ], + "'rimmed ' vacuole on biopsy": [ + "HP:0003805" + ], + "'rimmed ' vacuoles on biopsy": [ + "HP:0003805" + ], + "abnormal muscle tone": [ + "HP:0003808" + ], + "reduce intrathoracic adipose tissue": [ + "HP:0003809" + ], + "reduced intrathoracic adipose tissue": [ + "HP:0003809" + ], + "late - onset distal muscle weakness": [ + "HP:0003810" + ], + "neonatal death": [ + "HP:0003811" + ], + "neonatal lethal": [ + "HP:0003811" + ], + "phenotypic variability": [ + "HP:0003812" + ], + "clinical heterogeneity": [ + "HP:0003812" + ], + "highly variable clinical phenotype": [ + "HP:0003812" + ], + "highly variable phenotype": [ + "HP:0003812" + ], + "highly variable phenotype and severity": [ + "HP:0003812" + ], + "highly variable phenotype , even within family": [ + "HP:0003812" + ], + "highly variable phenotype , even within families": [ + "HP:0003812" + ], + "variable phenotype": [ + "HP:0003812" + ], + "variable phenotypic severity": [ + "HP:0003812" + ], + "death in childhood": [ + "HP:0003819" + ], + "stillbirth": [ + "HP:0003826" + ], + "fetal death": [ + "HP:0003826" + ], + "foetal death": [ + "HP:0003826" + ], + "stillborn": [ + "HP:0003826" + ], + "variable expressivity": [ + "HP:0003828" + ], + "highly variable severity": [ + "HP:0003828" + ], + "variable severity": [ + "HP:0003828" + ], + "incomplete penetrance": [ + "HP:0003829" + ], + "reduce penetrance": [ + "HP:0003829" + ], + "reduced penetrance": [ + "HP:0003829" + ], + "age - dependent penetrance": [ + "HP:0003831" + ], + "age dependent penetrance": [ + "HP:0003831" + ], + "abnormality of the tibial plateau": [ + "HP:0003832" + ], + "abnormality of the tibial plateaux": [ + "HP:0003832" + ], + "laterally deficient tibial plateau": [ + "HP:0003833" + ], + "laterally deficient tibial plateaux": [ + "HP:0003833" + ], + "shoulder dislocation": [ + "HP:0003834" + ], + "shoulder subluxation": [ + "HP:0003835" + ], + "partial shoulder dislocation": [ + "HP:0003835" + ], + "stipple calcification of the shoulder": [ + "HP:0003836" + ], + "stippled calcification of the shoulder": [ + "HP:0003836" + ], + "soft - tissue ossification around the shoulder": [ + "HP:0003837" + ], + "soft - tissue ossification around the shoulders": [ + "HP:0003837" + ], + "calcification of the soft - tissue around the shoulder": [ + "HP:0003837" + ], + "calcification of the soft - tissue around the shoulders": [ + "HP:0003837" + ], + "abnormality of upper limb epiphysis morphology": [ + "HP:0003839" + ], + "abnormal shape of end part of upper limb long bone": [ + "HP:0003839" + ], + "abnormal shape of end part of upper limb long bones": [ + "HP:0003839" + ], + "abnormality involve the epiphysis of the upper limb": [ + "HP:0003839" + ], + "abnormality involving the epiphyses of the upper limbs": [ + "HP:0003839" + ], + "epihyseal plate abnormality of the upper limb": [ + "HP:0003839" + ], + "epihyseal plate abnormality of the upper limbs": [ + "HP:0003839" + ], + "delay upper limb epiphyseal ossification": [ + "HP:0003840" + ], + "delayed upper limb epiphyseal ossification": [ + "HP:0003840" + ], + "delay maturation fo the end part of the upper limb bone": [ + "HP:0003840" + ], + "delayed maturation fo the end part of the upper limb bone": [ + "HP:0003840" + ], + "fragmented epiphysis of the upper limb": [ + "HP:0003841" + ], + "fragmented epiphyses of the upper limbs": [ + "HP:0003841" + ], + "fragmented end part of upper limb bone": [ + "HP:0003841" + ], + "fragmented end part of upper limb bones": [ + "HP:0003841" + ], + "irregular epiphysis of the upper limb": [ + "HP:0003842" + ], + "irregular epiphyses of the upper limbs": [ + "HP:0003842" + ], + "irregular end part of upper limb bone": [ + "HP:0003842" + ], + "irregular end part of upper limb bones": [ + "HP:0003842" + ], + "round epiphysis of the upper limb": [ + "HP:0003843" + ], + "round epiphyses of the upper limbs": [ + "HP:0003843" + ], + "round end part of upper limb bone": [ + "HP:0003843" + ], + "round end part of upper limb bones": [ + "HP:0003843" + ], + "small epiphysis of the upper limb": [ + "HP:0003844" + ], + "small epiphyses of the upper limbs": [ + "HP:0003844" + ], + "small end part of upper limb bone": [ + "HP:0003844" + ], + "small end part of upper limb bones": [ + "HP:0003844" + ], + "wide epiphyseal plate of the upper limb": [ + "HP:0003846" + ], + "wide epiphyseal plates of the upper limbs": [ + "HP:0003846" + ], + "broad epiphyseal plate of the upper limb": [ + "HP:0003846" + ], + "broad epiphyseal plates of the upper limbs": [ + "HP:0003846" + ], + "broad growth plate of upper limb": [ + "HP:0003846" + ], + "broad growth plates of upper limbs": [ + "HP:0003846" + ], + "cupped metaphyses of the upper limb": [ + "HP:0003848" + ], + "cupped metaphyses of the upper limbs": [ + "HP:0003848" + ], + "cup wide portion of the upper limb bone": [ + "HP:0003848" + ], + "cupped wide portion of the upper limb bone": [ + "HP:0003848" + ], + "flare upper limb metaphysis": [ + "HP:0003849" + ], + "flared upper limb metaphysis": [ + "HP:0003849" + ], + "flared metaphyses of the upper limb": [ + "HP:0003849" + ], + "flared metaphyses of the upper limbs": [ + "HP:0003849" + ], + "flare wide portion of the upper limb bone": [ + "HP:0003849" + ], + "flared wide portion of the upper limb bone": [ + "HP:0003849" + ], + "upper - limb metaphyseal irregularity": [ + "HP:0003850" + ], + "irregular metaphyses of the upper limb": [ + "HP:0003850" + ], + "irregular metaphyses of the upper limbs": [ + "HP:0003850" + ], + "irregular wide portion of upper limb bone": [ + "HP:0003850" + ], + "irregular wide portion of upper limb bones": [ + "HP:0003850" + ], + "lytic defect in metaphyses of the upper limb": [ + "HP:0003851" + ], + "lytic defects in metaphyses of the upper limbs": [ + "HP:0003851" + ], + "normal density transverse band in metaphyses of the upper limb": [ + "HP:0003852" + ], + "normal density transverse bands in metaphyses of the upper limbs": [ + "HP:0003852" + ], + "sclerosis with transverse striation in metaphyses of the upper limb": [ + "HP:0003853" + ], + "sclerosis with transverse striations in metaphyses of the upper limbs": [ + "HP:0003853" + ], + "sclerosis of metaphyses of the upper limb": [ + "HP:0003854" + ], + "sclerosis of metaphyses of the upper limbs": [ + "HP:0003854" + ], + "increase bone density in wide portion of the upper limb bone": [ + "HP:0003854" + ], + "increased bone density in wide portion of the upper limb bones": [ + "HP:0003854" + ], + "spurred metaphyses of the upper limb": [ + "HP:0003855" + ], + "spurred metaphyses of the upper limbs": [ + "HP:0003855" + ], + "spur wide portion of upper limb bone": [ + "HP:0003855" + ], + "spurred wide portion of upper limb bone": [ + "HP:0003855" + ], + "upper limb metaphyseal widening": [ + "HP:0003856" + ], + "broad wide portion of upper limb bone": [ + "HP:0003856" + ], + "wide / broad metaphyses of the upper limb": [ + "HP:0003856" + ], + "wide / broad metaphyses of the upper limbs": [ + "HP:0003856" + ], + "cortical diaphyseal irregularity of the upper limb": [ + "HP:0003858" + ], + "cortical diaphyseal irregularity of the upper limbs": [ + "HP:0003858" + ], + "cortical diaphyseal thickening of the upper limb": [ + "HP:0003859" + ], + "cortical diaphyseal thickening of the upper limbs": [ + "HP:0003859" + ], + "diaphyseal sclerosis of the upper limb": [ + "HP:0003860" + ], + "diaphyseal sclerosis of the upper limbs": [ + "HP:0003860" + ], + "increase bone density in central part of long bone of upper limb": [ + "HP:0003860" + ], + "increased bone density in central part of long bone of upper limbs": [ + "HP:0003860" + ], + "broad diaphysis of the upper limb": [ + "HP:0003861" + ], + "broad diaphyses of the upper limbs": [ + "HP:0003861" + ], + "broad shaft of long bone of the upper limb": [ + "HP:0003861" + ], + "broad shaft of long bone of the upper limbs": [ + "HP:0003861" + ], + "wide diaphysis of the upper limb": [ + "HP:0003861" + ], + "wide diaphyses of the upper limbs": [ + "HP:0003861" + ], + "wide shaft of long bone of the upper limb": [ + "HP:0003861" + ], + "wide shaft of long bone of the upper limbs": [ + "HP:0003861" + ], + "absent humerus": [ + "HP:0003862" + ], + "absent long bone in upper arm": [ + "HP:0003862" + ], + "aplasia of the humerus": [ + "HP:0003862" + ], + "aplastic humerus": [ + "HP:0003862" + ], + "angulate humerus": [ + "HP:0003863" + ], + "angulated humerus": [ + "HP:0003863" + ], + "angulate long bone in upper arm": [ + "HP:0003863" + ], + "angulated long bone in upper arm": [ + "HP:0003863" + ], + "bifid humerus": [ + "HP:0003864" + ], + "notch long bone in upper arm": [ + "HP:0003864" + ], + "notched long bone in upper arm": [ + "HP:0003864" + ], + "bow humerus": [ + "HP:0003865" + ], + "bowed humerus": [ + "HP:0003865" + ], + "bow long bone in upper arm": [ + "HP:0003865" + ], + "bowed long bone in upper arm": [ + "HP:0003865" + ], + "bowing of the humerus": [ + "HP:0003865" + ], + "humeral bowing": [ + "HP:0003865" + ], + "coarse humeral trabecula": [ + "HP:0003866" + ], + "coarse humeral trabeculae": [ + "HP:0003866" + ], + "humeral cortical irregularity": [ + "HP:0003867" + ], + "humeral cortical thickening": [ + "HP:0003868" + ], + "humeral cortical thinning": [ + "HP:0003869" + ], + "crumple humerus": [ + "HP:0003870" + ], + "crumpled humerus": [ + "HP:0003870" + ], + "crumple long bone in upper arm": [ + "HP:0003870" + ], + "crumpled long bone in upper arm": [ + "HP:0003870" + ], + "deform humerus": [ + "HP:0003871" + ], + "deformed humerus": [ + "HP:0003871" + ], + "deform long bone in upper arm": [ + "HP:0003871" + ], + "deformed long bone in upper arm": [ + "HP:0003871" + ], + "humeral exostosis": [ + "HP:0003872" + ], + "humeral exostoses": [ + "HP:0003872" + ], + "humerus varus": [ + "HP:0003874" + ], + "humeral lytic defect": [ + "HP:0003875" + ], + "humeral lytic defects": [ + "HP:0003875" + ], + "lytic defect of the humerus": [ + "HP:0003875" + ], + "lytic defects of the humerus": [ + "HP:0003875" + ], + "osteoporotic humerus": [ + "HP:0003876" + ], + "oval transradiancy of humerus": [ + "HP:0003877" + ], + "humeral oval transradiancy": [ + "HP:0003877" + ], + "periosteal new bone of humerus": [ + "HP:0003878" + ], + "humeral pseudarthrosis": [ + "HP:0003879" + ], + "false joint ( long bone in upper arm )": [ + "HP:0003879" + ], + "sclerotic focus of the humerus": [ + "HP:0003880" + ], + "sclerotic foci of the humerus": [ + "HP:0003880" + ], + "humeral sclerotic focus": [ + "HP:0003880" + ], + "humeral sclerotic foci": [ + "HP:0003880" + ], + "humeral sclerosis": [ + "HP:0003881" + ], + "increase bone density in long bone of upper arm": [ + "HP:0003881" + ], + "increased bone density in long bone of upper arm": [ + "HP:0003881" + ], + "sclerosis of humerus": [ + "HP:0003881" + ], + "slender humerus": [ + "HP:0003882" + ], + "slender long bone of upper arm": [ + "HP:0003882" + ], + "taper humerus": [ + "HP:0003883" + ], + "tapered humerus": [ + "HP:0003883" + ], + "taper long bone of upper arm": [ + "HP:0003883" + ], + "tapered long bone of upper arm": [ + "HP:0003883" + ], + "triangular humerus": [ + "HP:0003884" + ], + "triangular long bone of upper arm": [ + "HP:0003884" + ], + "undermodeled humerus": [ + "HP:0003885" + ], + "wide humerus": [ + "HP:0003886" + ], + "broad humerus": [ + "HP:0003886" + ], + "wide long bone of upper arm": [ + "HP:0003886" + ], + "abnormality of the humeral head": [ + "HP:0003887" + ], + "abnormality of the humeral heads": [ + "HP:0003887" + ], + "abnormal head of long bone in upper arm": [ + "HP:0003887" + ], + "flatten humeral head": [ + "HP:0003888" + ], + "flattened humeral heads": [ + "HP:0003888" + ], + "flattended head of long bone in upper arm": [ + "HP:0003888" + ], + "abnormality of the deltoid tuberosity": [ + "HP:0003889" + ], + "abnormality of the deltoid tuberosities": [ + "HP:0003889" + ], + "prominent deltoid tuberosity": [ + "HP:0003890" + ], + "prominent deltoid tuberosities": [ + "HP:0003890" + ], + "abnormality of the humeral epiphysis": [ + "HP:0003891" + ], + "abnormality of end part of the long bone of the upper arm": [ + "HP:0003891" + ], + "abnormality of the humeral epiphyses": [ + "HP:0003891" + ], + "absent humeral epiphyseal ossification": [ + "HP:0003892" + ], + "absent maturation of end part of long bone in upper arm": [ + "HP:0003892" + ], + "absent ossification of the humeral epiphysis": [ + "HP:0003892" + ], + "absent ossification of the humeral epiphyses": [ + "HP:0003892" + ], + "advanced ossification of the humeral epiphysis": [ + "HP:0003893" + ], + "accelerate maturation of end part of long bone in upper arm": [ + "HP:0003893" + ], + "accelerated maturation of end part of long bone in upper arm": [ + "HP:0003893" + ], + "advanced maturation of the humeral epiphysis": [ + "HP:0003893" + ], + "advanced maturation of the humeral epiphyses": [ + "HP:0003893" + ], + "delay humeral epiphyseal ossification": [ + "HP:0003894" + ], + "delayed humeral epiphyseal ossification": [ + "HP:0003894" + ], + "delay maturation of the end part of the long bone in upper arm": [ + "HP:0003894" + ], + "delayed maturation of the end part of the long bone in upper arm": [ + "HP:0003894" + ], + "delay maturation / delay ossification of the humeral epiphysis": [ + "HP:0003894" + ], + "delayed maturation / delayed ossification of the humeral epiphyses": [ + "HP:0003894" + ], + "flatten humeral epiphysis": [ + "HP:0003895" + ], + "flattened humeral epiphyses": [ + "HP:0003895" + ], + "flatten end part of long bone in upper arm": [ + "HP:0003895" + ], + "flattened end part of long bone in upper arm": [ + "HP:0003895" + ], + "irregular humeral epiphysis": [ + "HP:0003896" + ], + "irregular humeral epiphyses": [ + "HP:0003896" + ], + "irregular end part of long bone in upper arm": [ + "HP:0003896" + ], + "irregular ossification of the humeral epiphysis": [ + "HP:0003897" + ], + "irregular ossification of the humeral epiphyses": [ + "HP:0003897" + ], + "irregular maturation of the end part of the long bone in upper arm": [ + "HP:0003897" + ], + "large humeral epiphysis": [ + "HP:0003898" + ], + "large humeral epiphyses": [ + "HP:0003898" + ], + "large end part of long bone in upper arm": [ + "HP:0003898" + ], + "round humeral epiphysis": [ + "HP:0003899" + ], + "round humeral epiphyses": [ + "HP:0003899" + ], + "round end part of long bone in upper arm": [ + "HP:0003899" + ], + "small humeral epiphysis": [ + "HP:0003900" + ], + "small humeral epiphyses": [ + "HP:0003900" + ], + "small end part of long bone in upper arm": [ + "HP:0003900" + ], + "stipple calcification of the humeral epiphysis": [ + "HP:0003901" + ], + "stippled calcification of the humeral epiphyses": [ + "HP:0003901" + ], + "epiphyseal stippling of the humerus": [ + "HP:0003902" + ], + "stipple ossification of the humeral epiphysis": [ + "HP:0003902" + ], + "stippled ossification of the humeral epiphyses": [ + "HP:0003902" + ], + "broad humeral epiphysis": [ + "HP:0003903" + ], + "broad humeral epiphyses": [ + "HP:0003903" + ], + "wide end part of long bone in upper arm": [ + "HP:0003903" + ], + "wide humeral epiphysis": [ + "HP:0003903" + ], + "wide humeral epiphyses": [ + "HP:0003903" + ], + "wide epiphysis of the upper limb": [ + "HP:0003904" + ], + "wide epiphyses of the upper limbs": [ + "HP:0003904" + ], + "broad epiphysis of the upper limb": [ + "HP:0003904" + ], + "broad epiphyses of the upper limbs": [ + "HP:0003904" + ], + "wide end part of upper limb bone": [ + "HP:0003904" + ], + "wide end part of upper limb bones": [ + "HP:0003904" + ], + "abnormality of the humeral epiphyseal plate": [ + "HP:0003905" + ], + "abnormality of arm long bone growth plate": [ + "HP:0003905" + ], + "broad humeral epiphyseal plate": [ + "HP:0003906" + ], + "wide humeral epiphyseal plate": [ + "HP:0003906" + ], + "wide long bone of arm growth plate": [ + "HP:0003906" + ], + "abnormality of the humeral metaphyses": [ + "HP:0003907" + ], + "abnormality of the wide portion of the long bone in upper arm": [ + "HP:0003907" + ], + "corner fracture of metaphysis": [ + "HP:0003908" + ], + "bucket handle fracture": [ + "HP:0003908" + ], + "metaphyseal corner fracture": [ + "HP:0003908" + ], + "cortical subperiosteal resorption of humeral metaphyses": [ + "HP:0003909" + ], + "enlarged humeral metaphyses": [ + "HP:0003910" + ], + "enlarge wide portion of long bone of upper arm": [ + "HP:0003910" + ], + "enlarged wide portion of long bone of upper arm": [ + "HP:0003910" + ], + "expand humeral metaphyses": [ + "HP:0003910" + ], + "expanded humeral metaphyses": [ + "HP:0003910" + ], + "flared humeral metaphysis": [ + "HP:0003911" + ], + "flare humerus": [ + "HP:0003911" + ], + "flared humerus": [ + "HP:0003911" + ], + "flare wide portion of long bone of upper arm": [ + "HP:0003911" + ], + "flared wide portion of long bone of upper arm": [ + "HP:0003911" + ], + "wide / broad humeral metaphysis": [ + "HP:0003911" + ], + "frayed humeral metaphyses": [ + "HP:0003912" + ], + "humeral metaphyseal irregularity": [ + "HP:0003913" + ], + "irregular humeral metaphyses": [ + "HP:0003913" + ], + "irregular wide portion of long bone in upper arm": [ + "HP:0003913" + ], + "irregular ossification of humeral metaphyses": [ + "HP:0003914" + ], + "irregular bone maturation of the wide portion of the long bone in upper arm": [ + "HP:0003914" + ], + "lytic defect of the humeral metaphysis": [ + "HP:0003915" + ], + "lytic defects of the humeral metaphysis": [ + "HP:0003915" + ], + "normal - density transverse humeral band": [ + "HP:0003916" + ], + "normal - density transverse humeral bands": [ + "HP:0003916" + ], + "point humeral metaphysis": [ + "HP:0003917" + ], + "pointed humeral metaphysis": [ + "HP:0003917" + ], + "point wide portion of long bone of upper arm": [ + "HP:0003917" + ], + "pointed wide portion of long bone of upper arm": [ + "HP:0003917" + ], + "sclerotic humeral metaphysis": [ + "HP:0003918" + ], + "hardening of wide portion of long bone of upper arm": [ + "HP:0003918" + ], + "stiffening of wide portion of long bone of upper arm": [ + "HP:0003918" + ], + "sclerotic humeral metaphysis with longitudinal striation": [ + "HP:0003919" + ], + "sclerotic humeral metaphysis with longitudinal striations": [ + "HP:0003919" + ], + "slop humeral metaphysis": [ + "HP:0003920" + ], + "sloping humeral metaphysis": [ + "HP:0003920" + ], + "slop metaphysis of long bone of upper arm": [ + "HP:0003920" + ], + "sloping metaphysis of long bone of upper arm": [ + "HP:0003920" + ], + "laterally slop humeral metaphysis": [ + "HP:0003921" + ], + "laterally sloping humeral metaphysis": [ + "HP:0003921" + ], + "laterally slop metaphysis of long bone of upper arm": [ + "HP:0003921" + ], + "laterally sloping metaphysis of long bone of upper arm": [ + "HP:0003921" + ], + "spur humeral metaphysis": [ + "HP:0003922" + ], + "spurred humeral metaphysis": [ + "HP:0003922" + ], + "spur metaphysis of long bone of upper arm": [ + "HP:0003922" + ], + "spurred metaphysis of long bone of upper arm": [ + "HP:0003922" + ], + "square humeral metaphysis": [ + "HP:0003923" + ], + "square metaphysis of long bone of upper arm": [ + "HP:0003923" + ], + "stipple calcification of humeral metaphysis": [ + "HP:0003924" + ], + "stippled calcification of humeral metaphysis": [ + "HP:0003924" + ], + "speckle calcification in metaphysis of long bone of upper arm": [ + "HP:0003924" + ], + "speckled calcification in metaphysis of long bone of upper arm": [ + "HP:0003924" + ], + "abnormality of the humeral diaphysis": [ + "HP:0003926" + ], + "abnormality of shaft of long bone in upper arm": [ + "HP:0003926" + ], + "cortical irregularity of humeral diaphysis": [ + "HP:0003927" + ], + "cortical thickening of humeral diaphysis": [ + "HP:0003928" + ], + "ground glass opacity of humeral diaphysis": [ + "HP:0003929" + ], + "lytic defect of humeral diaphysis": [ + "HP:0003930" + ], + "lytic defects of humeral diaphysis": [ + "HP:0003930" + ], + "humeral diaphyseal lysis": [ + "HP:0003930" + ], + "periosteal new bone of humeral diaphysis": [ + "HP:0003931" + ], + "sclerotic focus of humeral diaphysis": [ + "HP:0003932" + ], + "sclerotic foci of humeral diaphysis": [ + "HP:0003932" + ], + "sclerosis of humeral diaphysis": [ + "HP:0003933" + ], + "increase bone density in shaft of long bone in upper arm": [ + "HP:0003933" + ], + "increased bone density in shaft of long bone in upper arm": [ + "HP:0003933" + ], + "slender humeral diaphysis": [ + "HP:0003934" + ], + "slender shaft of long bone in upper arm": [ + "HP:0003934" + ], + "wide humeral diaphysis": [ + "HP:0003935" + ], + "broad humeral diaphysis": [ + "HP:0003935" + ], + "broad shaft of long bone in upper arm": [ + "HP:0003935" + ], + "wide shaft of long bone in upper arm": [ + "HP:0003935" + ], + "synostosis involve the elbow": [ + "HP:0003938" + ], + "synostosis involving the elbow": [ + "HP:0003938" + ], + "bone fusion involve the elbow": [ + "HP:0003938" + ], + "bone fusion involving the elbow": [ + "HP:0003938" + ], + "humeroulnar synostosis": [ + "HP:0003939" + ], + "humeral ulnar synostosis": [ + "HP:0003939" + ], + "osteoarthritis of the elbow": [ + "HP:0003940" + ], + "stipple calcification of the elbow": [ + "HP:0003941" + ], + "stippled calcification of the elbow": [ + "HP:0003941" + ], + "synovial chondromatosis of the elbow": [ + "HP:0003942" + ], + "abnormality of the joint space of the elbow": [ + "HP:0003943" + ], + "abnormality of the joint spaces of the elbow": [ + "HP:0003943" + ], + "narrow joint space of the elbow": [ + "HP:0003944" + ], + "narrow joint spaces of the elbow": [ + "HP:0003944" + ], + "irregular articular surface of the elbow joint": [ + "HP:0003945" + ], + "irregular articular surfaces of the elbow joints": [ + "HP:0003945" + ], + "abnormality of the epiphysis of the elbow": [ + "HP:0003946" + ], + "abnormality of the epiphyses of the elbow": [ + "HP:0003946" + ], + "abnormality of end part of the elbow bone": [ + "HP:0003946" + ], + "delay elbow epiphyseal ossification": [ + "HP:0003947" + ], + "delayed elbow epiphyseal ossification": [ + "HP:0003947" + ], + "delay maturation of the end part of the elbow bone": [ + "HP:0003947" + ], + "delayed maturation of the end part of the elbow bone": [ + "HP:0003947" + ], + "irregular epiphysis of the elbow": [ + "HP:0003948" + ], + "irregular epiphyses of the elbow": [ + "HP:0003948" + ], + "irregular end part of the elbow bone": [ + "HP:0003948" + ], + "abnormality of the elbow metaphyses": [ + "HP:0003949" + ], + "abnormal wide portion of elbow bone": [ + "HP:0003949" + ], + "flare elbow metaphyses": [ + "HP:0003950" + ], + "flared elbow metaphyses": [ + "HP:0003950" + ], + "flare wide portion of elbow bone": [ + "HP:0003950" + ], + "flared wide portion of elbow bone": [ + "HP:0003950" + ], + "distal humeral metaphyseal irregularity": [ + "HP:0003951" + ], + "irregular metaphyses of elbow": [ + "HP:0003951" + ], + "irregular wide portion of elbow bone": [ + "HP:0003951" + ], + "sclerotic focus of metaphyses of the elbow": [ + "HP:0003952" + ], + "sclerotic foci of metaphyses of the elbow": [ + "HP:0003952" + ], + "vertical linear mixed lucent and sclerotic pattern of metaphyses": [ + "HP:0003952" + ], + "absent forearm bone": [ + "HP:0003953" + ], + "aplasia of the forearm bone": [ + "HP:0003953" + ], + "aplasia of the forearm bones": [ + "HP:0003953" + ], + "angulate forearm bone": [ + "HP:0003954" + ], + "angulated forearm bones": [ + "HP:0003954" + ], + "bone - in - a - bone appearance of forearm": [ + "HP:0003955" + ], + "bow forearm bone": [ + "HP:0003956" + ], + "bowed forearm bones": [ + "HP:0003956" + ], + "cortical thickening of the forearm bone": [ + "HP:0003957" + ], + "cortical thickening of the forearm bones": [ + "HP:0003957" + ], + "cross - fusion of the forearm bone": [ + "HP:0003958" + ], + "cross - fusion of the forearm bones": [ + "HP:0003958" + ], + "deform forearm bone": [ + "HP:0003959" + ], + "deformed forearm bones": [ + "HP:0003959" + ], + "exostosis of the forearm bone": [ + "HP:0003960" + ], + "exostoses of the forearm bones": [ + "HP:0003960" + ], + "fracture forearm bone": [ + "HP:0003961" + ], + "fractured forearm bones": [ + "HP:0003961" + ], + "broken forearm": [ + "HP:0003961" + ], + "fracture of the forearm": [ + "HP:0003961" + ], + "lytic defect of the forearm bone": [ + "HP:0003963" + ], + "lytic defects of the forearm bones": [ + "HP:0003963" + ], + "osteoporotic forearm bone": [ + "HP:0003964" + ], + "osteoporotic forearm bones": [ + "HP:0003964" + ], + "pseudarthrosis of the forearm bone": [ + "HP:0003965" + ], + "pseudarthrosis of the forearm bones": [ + "HP:0003965" + ], + "sclerotic focus in forearm bone": [ + "HP:0003966" + ], + "sclerotic foci in forearm bones": [ + "HP:0003966" + ], + "sclerotic forearm bone": [ + "HP:0003967" + ], + "sclerotic forearm bones": [ + "HP:0003967" + ], + "increase bone density of forearm bone": [ + "HP:0003967" + ], + "increased bone density of forearm bones": [ + "HP:0003967" + ], + "slender forearm bone": [ + "HP:0003969" + ], + "slender forearm bones": [ + "HP:0003969" + ], + "undermodelled forearm bone": [ + "HP:0003970" + ], + "undermodelled forearm bones": [ + "HP:0003970" + ], + "broad forearm bone": [ + "HP:0003971" + ], + "broad forearm bones": [ + "HP:0003971" + ], + "wide forearm bone": [ + "HP:0003971" + ], + "wide forearm bones": [ + "HP:0003971" + ], + "wide radioulnar joint": [ + "HP:0003973" + ], + "wide radioulnar joints": [ + "HP:0003973" + ], + "broad radioulnar joint": [ + "HP:0003973" + ], + "broad radioulnar joints": [ + "HP:0003973" + ], + "absent radius": [ + "HP:0003974" + ], + "absence of radius and ulna": [ + "HP:0003974" + ], + "absent ossification / absence of radius": [ + "HP:0003974" + ], + "aplasia of the radius": [ + "HP:0003974" + ], + "miss outer large bone of forearm": [ + "HP:0003974" + ], + "missing outer large bone of forearm": [ + "HP:0003974" + ], + "radial aplasia": [ + "HP:0003974" + ], + "obsolete chevron - shape / cone - shape radius": [ + "HP:0003975" + ], + "obsolete chevron - shaped / cone - shaped radius": [ + "HP:0003975" + ], + "constrict radius": [ + "HP:0003976" + ], + "constricted radius": [ + "HP:0003976" + ], + "deform radius": [ + "HP:0003977" + ], + "deformed radius": [ + "HP:0003977" + ], + "fracture radius": [ + "HP:0003978" + ], + "fractured radius": [ + "HP:0003978" + ], + "lytic defect of the radius": [ + "HP:0003979" + ], + "lytic defects of the radius": [ + "HP:0003979" + ], + "pseudarthrosis of the radius": [ + "HP:0003980" + ], + "broad radius": [ + "HP:0003981" + ], + "wide radius": [ + "HP:0003981" + ], + "aplasia of the ulna": [ + "HP:0003982" + ], + "absent ossification / absent ulna": [ + "HP:0003982" + ], + "absent ulna": [ + "HP:0003982" + ], + "absent ulnae": [ + "HP:0003982" + ], + "posteriorly dislocate ulna": [ + "HP:0003984" + ], + "posteriorly dislocated ulna": [ + "HP:0003984" + ], + "exostosis of the ulna": [ + "HP:0003985" + ], + "exostoses of the ulna": [ + "HP:0003985" + ], + "exostosis of the radius": [ + "HP:0003986" + ], + "exostoses of the radius": [ + "HP:0003986" + ], + "fracture ulna": [ + "HP:0003987" + ], + "fractured ulna": [ + "HP:0003987" + ], + "long ulna": [ + "HP:0003988" + ], + "disproportionately long ulna": [ + "HP:0003988" + ], + "disproportionately long ulnae": [ + "HP:0003988" + ], + "notch ulna": [ + "HP:0003989" + ], + "notched ulna": [ + "HP:0003989" + ], + "point ulna": [ + "HP:0003990" + ], + "pointed ulna": [ + "HP:0003990" + ], + "osteosclerosis of the ulna": [ + "HP:0003991" + ], + "sclerotic ulna": [ + "HP:0003991" + ], + "slender ulna": [ + "HP:0003992" + ], + "broad ulna": [ + "HP:0003993" + ], + "wide ulna": [ + "HP:0003993" + ], + "dislocate wrist": [ + "HP:0003994" + ], + "dislocated wrist": [ + "HP:0003994" + ], + "dislocation of the wrist": [ + "HP:0003994" + ], + "dislocations of the wrists": [ + "HP:0003994" + ], + "abnormality of the radial head": [ + "HP:0003995" + ], + "deformity of radial head": [ + "HP:0003995" + ], + "deformity of radial heads": [ + "HP:0003995" + ], + "flatten radial head": [ + "HP:0003996" + ], + "flattened radial head": [ + "HP:0003996" + ], + "hypoplastic radial head": [ + "HP:0003997" + ], + "small radial head": [ + "HP:0003997" + ], + "constrict radial neck": [ + "HP:0003998" + ], + "constricted radial neck": [ + "HP:0003998" + ], + "abnormality of radial epiphysis": [ + "HP:0003999" + ], + "abnormality of radial epiphyses": [ + "HP:0003999" + ], + "abnormality of radial epiphyseal plate": [ + "HP:0003999" + ], + "abnormality of radial epiphyseal plates": [ + "HP:0003999" + ], + "cone - shaped distal radial epiphysis": [ + "HP:0004000" + ], + "chevron - shaped distal radial epiphysis": [ + "HP:0004000" + ], + "medially deficient radial epiphysis": [ + "HP:0004001" + ], + "medially deficient radial epiphyses": [ + "HP:0004001" + ], + "flatten radial epiphysis": [ + "HP:0004002" + ], + "flattened radial epiphyses": [ + "HP:0004002" + ], + "medially flatten radial epiphysis": [ + "HP:0004003" + ], + "medially flattened radial epiphyses": [ + "HP:0004003" + ], + "irregular radial epiphysis": [ + "HP:0004004" + ], + "irregular radial epiphyses": [ + "HP:0004004" + ], + "large radial epiphysis": [ + "HP:0004005" + ], + "large radial epiphyses": [ + "HP:0004005" + ], + "round radial epiphysis": [ + "HP:0004006" + ], + "round radial epiphyses": [ + "HP:0004006" + ], + "sclerotic radial epiphysis": [ + "HP:0004007" + ], + "sclerotic radial epiphyses": [ + "HP:0004007" + ], + "slop radial epiphysis": [ + "HP:0004008" + ], + "sloping radial epiphyses": [ + "HP:0004008" + ], + "medially slop radial epiphysis": [ + "HP:0004009" + ], + "medially sloping radial epiphyses": [ + "HP:0004009" + ], + "small radial epiphysis": [ + "HP:0004010" + ], + "small radial epiphyses": [ + "HP:0004010" + ], + "premature fusion of the radial epiphyseal plate": [ + "HP:0004012" + ], + "premature fusion of the radial epiphyseal plates": [ + "HP:0004012" + ], + "medially fuse radial epiphyseal plate": [ + "HP:0004013" + ], + "medially fused radial epiphyseal plates": [ + "HP:0004013" + ], + "broad radial epiphyseal plate": [ + "HP:0004014" + ], + "wide radial epiphyseal plate": [ + "HP:0004014" + ], + "wide radial epiphyseal plates": [ + "HP:0004014" + ], + "abnormality of radial metaphyses": [ + "HP:0004015" + ], + "cup radial metaphyses": [ + "HP:0004016" + ], + "cupped radial metaphyses": [ + "HP:0004016" + ], + "exostosis of the radial metaphysis": [ + "HP:0004017" + ], + "exostoses of the radial metaphysis": [ + "HP:0004017" + ], + "flare radial metaphysis": [ + "HP:0004018" + ], + "flared radial metaphysis": [ + "HP:0004018" + ], + "broadening of the distal radius": [ + "HP:0004018" + ], + "radial metaphyseal irregularity": [ + "HP:0004019" + ], + "irregular radial metaphysis": [ + "HP:0004019" + ], + "irregular ossification of the radial metaphysis": [ + "HP:0004020" + ], + "lytic defect of radial metaphysis": [ + "HP:0004021" + ], + "lytic defects of radial metaphysis": [ + "HP:0004021" + ], + "sclerotic radial metaphysis with longitudinal striation": [ + "HP:0004022" + ], + "sclerotic radial metaphysis with longitudinal striations": [ + "HP:0004022" + ], + "slop radial metaphysis": [ + "HP:0004023" + ], + "sloping radial metaphysis": [ + "HP:0004023" + ], + "medially slop radial metaphysis": [ + "HP:0004024" + ], + "medially sloping radial metaphysis": [ + "HP:0004024" + ], + "spur radial metaphysis": [ + "HP:0004025" + ], + "spurred radial metaphysis": [ + "HP:0004025" + ], + "broad radial metaphysis": [ + "HP:0004026" + ], + "wide radial metaphysis": [ + "HP:0004026" + ], + "abnormality of radial diaphysis": [ + "HP:0004027" + ], + "spur of radial diaphysis": [ + "HP:0004028" + ], + "spurs of radial diaphysis": [ + "HP:0004028" + ], + "lytic defect of radial diaphysis": [ + "HP:0004029" + ], + "lytic defects of radial diaphysis": [ + "HP:0004029" + ], + "patchy sclerosis of radial diaphysis": [ + "HP:0004030" + ], + "broad radial diaphysis": [ + "HP:0004031" + ], + "wide radial diaphysis": [ + "HP:0004031" + ], + "abnormality of the olecranon": [ + "HP:0004032" + ], + "curve olecranon": [ + "HP:0004033" + ], + "curved olecranon": [ + "HP:0004033" + ], + "irregular olecranon": [ + "HP:0004034" + ], + "abnormality of the styloid process of ulna": [ + "HP:0004035" + ], + "long styloid process of ulna": [ + "HP:0004036" + ], + "abnormality of the ulnar epiphysis": [ + "HP:0004037" + ], + "abnormality of the ulnar epiphyses": [ + "HP:0004037" + ], + "abnormality of the epiphyseal plate of the ulna": [ + "HP:0004037" + ], + "obsolete bony spicule of ulnar epiphyseal plate": [ + "HP:0004038" + ], + "abnormality of ulnar metaphysis": [ + "HP:0004039" + ], + "corner fragment of ulnar metaphysis": [ + "HP:0004040" + ], + "corner fragments of ulnar metaphysis": [ + "HP:0004040" + ], + "cup ulnar metaphysis": [ + "HP:0004041" + ], + "cupped ulnar metaphysis": [ + "HP:0004041" + ], + "ulnar metaphyseal irregularity": [ + "HP:0004042" + ], + "irregular ulnar metaphysis": [ + "HP:0004042" + ], + "lytic defect of ulnar metaphysis": [ + "HP:0004043" + ], + "lytic defects of ulnar metaphysis": [ + "HP:0004043" + ], + "point ulnar metaphysis": [ + "HP:0004044" + ], + "pointed ulnar metaphysis": [ + "HP:0004044" + ], + "slop ulnar metaphysis": [ + "HP:0004045" + ], + "sloping ulnar metaphysis": [ + "HP:0004045" + ], + "spur ulnar metaphysis": [ + "HP:0004046" + ], + "spurred ulnar metaphysis": [ + "HP:0004046" + ], + "wide ulnar metaphysis": [ + "HP:0004047" + ], + "broad ulnar metaphysis": [ + "HP:0004047" + ], + "narrow joint space of wrist": [ + "HP:0004048" + ], + "narrow joint spaces of wrist": [ + "HP:0004048" + ], + "decrease carpal angle of wrist": [ + "HP:0004049" + ], + "decreased carpal angles of wrist": [ + "HP:0004049" + ], + "absent hand": [ + "HP:0004050" + ], + "acheiria": [ + "HP:0004050" + ], + "advanced ossification of the hand bone": [ + "HP:0004051" + ], + "advanced ossification of the hand bones": [ + "HP:0004051" + ], + "accelerate maturation of hand bone": [ + "HP:0004051" + ], + "accelerated maturation of hand bones": [ + "HP:0004051" + ], + "advanced maturation of the hand bone": [ + "HP:0004051" + ], + "advanced maturation of the hand bones": [ + "HP:0004051" + ], + "delay ossification of the hand bone": [ + "HP:0004052" + ], + "delayed ossification of the hand bones": [ + "HP:0004052" + ], + "delay maturation / delay ossification of the hand": [ + "HP:0004052" + ], + "delay maturation / delayed ossification of the hand": [ + "HP:0004052" + ], + "delay maturation of the hand bone": [ + "HP:0004052" + ], + "delayed maturation of the hand bones": [ + "HP:0004052" + ], + "dysharmonic maturation of the hand bone": [ + "HP:0004053" + ], + "dysharmonic maturation of the hand bones": [ + "HP:0004053" + ], + "disharmonic maturation of the hand bone": [ + "HP:0004053" + ], + "disharmonic maturation of the hand bones": [ + "HP:0004053" + ], + "dysharmonic ossification of the hand bone": [ + "HP:0004053" + ], + "dysharmonic ossification of the hand bones": [ + "HP:0004053" + ], + "sclerosis of hand bone": [ + "HP:0004054" + ], + "generalised sclerosis of hand bone": [ + "HP:0004054" + ], + "generalised sclerosis of hand bones": [ + "HP:0004054" + ], + "generalized sclerosis of hand bone": [ + "HP:0004054" + ], + "generalized sclerosis of hand bones": [ + "HP:0004054" + ], + "hand bone sclerosis": [ + "HP:0004054" + ], + "increase bone density in hand bone": [ + "HP:0004054" + ], + "increased bone density in hand bone": [ + "HP:0004054" + ], + "increased bone density in hand bones": [ + "HP:0004054" + ], + "mitten deformity": [ + "HP:0004057" + ], + "pseudosyndactyly": [ + "HP:0004057" + ], + "hand monodactyly": [ + "HP:0004058" + ], + "radial club hand": [ + "HP:0004059" + ], + "trident hand": [ + "HP:0004060" + ], + "trident abnormality": [ + "HP:0004060" + ], + "trident deformity": [ + "HP:0004060" + ], + "obsolete laterally deviate thumb phalanx": [ + "HP:0004066" + ], + "obsolete laterally deviated thumb phalanges": [ + "HP:0004066" + ], + "obsolete laterally deviate terminal thumb phalanx": [ + "HP:0004083" + ], + "obsolete laterally deviated terminal thumb phalanx": [ + "HP:0004083" + ], + "obsolete advance maturation / advance ossification of terminal thumb phalanx epiphysis": [ + "HP:0004090" + ], + "obsolete advanced maturation / advanced ossification of terminal thumb phalanx epiphysis": [ + "HP:0004090" + ], + "curve finger": [ + "HP:0004095" + ], + "curved fingers": [ + "HP:0004095" + ], + "deviation of finger": [ + "HP:0004097" + ], + "atypical position of finger": [ + "HP:0004097" + ], + "deviate finger": [ + "HP:0004097" + ], + "deviated fingers": [ + "HP:0004097" + ], + "finger point in a different direction than usual": [ + "HP:0004097" + ], + "finger pointing in a different direction than usual": [ + "HP:0004097" + ], + "macrodactyly": [ + "HP:0004099" + ], + "finger overgrowth": [ + "HP:0004099" + ], + "megalodactyly": [ + "HP:0004099" + ], + "abnormal 2nd finger morphology": [ + "HP:0004100" + ], + "abnormality of index finger": [ + "HP:0004100" + ], + "abnormality of the 2nd finger": [ + "HP:0004100" + ], + "obsolete radially deviate index finger phalanx": [ + "HP:0004110" + ], + "obsolete radially deviated index finger phalanges": [ + "HP:0004110" + ], + "midline nasal groove": [ + "HP:0004112" + ], + "central nasal groove": [ + "HP:0004112" + ], + "obsolete radially displace proximal index finger phalanx": [ + "HP:0004121" + ], + "obsolete radially displaced proximal index finger phalanx": [ + "HP:0004121" + ], + "midline defect of the nose": [ + "HP:0004122" + ], + "central cleft of nose": [ + "HP:0004122" + ], + "central defect of nose": [ + "HP:0004122" + ], + "central nasal defect": [ + "HP:0004122" + ], + "midline cleft of nose": [ + "HP:0004122" + ], + "midline nasal defect": [ + "HP:0004122" + ], + "dimple on nasal tip": [ + "HP:0004132" + ], + "dimple tip of nose": [ + "HP:0004132" + ], + "dimpled tip of nose": [ + "HP:0004132" + ], + "obsolete metaphyseal abnormality of middle phalanx of the 2nd finger": [ + "HP:0004138" + ], + "obsolete flare metaphysis of middle phalanx of index finger": [ + "HP:0004139" + ], + "obsolete flared metaphysis of middle phalanx of index finger": [ + "HP:0004139" + ], + "obsolete radially deviate terminal index finger phalanx": [ + "HP:0004143" + ], + "obsolete radially deviated terminal index finger phalanx": [ + "HP:0004143" + ], + "obsolete duplication of terminal index finger phalanx": [ + "HP:0004144" + ], + "abnormal 3rd finger morphology": [ + "HP:0004150" + ], + "abnormality of the 3rd finger": [ + "HP:0004150" + ], + "abnormality of the middle finger": [ + "HP:0004150" + ], + "obsolete overgrowth of middle finger": [ + "HP:0004153" + ], + "obsolete accessory middle - finger phalanx": [ + "HP:0004157" + ], + "obsolete accessory middle - finger phalanges": [ + "HP:0004157" + ], + "obsolete periosteal new bone of middle finger phalanx": [ + "HP:0004161" + ], + "obsolete periosteal new bone of middle finger phalanges": [ + "HP:0004161" + ], + "obsolete radially point middle finger phalanx": [ + "HP:0004162" + ], + "obsolete radially pointed middle finger phalanges": [ + "HP:0004162" + ], + "obsolete radially point proximal middle - finger phalanx": [ + "HP:0004168" + ], + "obsolete radially pointed proximal middle - finger phalanx": [ + "HP:0004168" + ], + "abnormality of the middle phalanx of the 3rd finger": [ + "HP:0004172" + ], + "abnormal middle finger bone of the middle finger": [ + "HP:0004172" + ], + "obsolete accessory middle phalanx of middle finger": [ + "HP:0004174" + ], + "obsolete periosteal new bone of middle phalanx of middle - finger": [ + "HP:0004175" + ], + "short distal phalanx of the 3rd finger": [ + "HP:0004180" + ], + "hypoplastic / small distal phalanx of the 3rd finger": [ + "HP:0004180" + ], + "short distal phalanx of the third finger": [ + "HP:0004180" + ], + "short outermost bone of the middle finger": [ + "HP:0004180" + ], + "short terminal phalanx of middle finger": [ + "HP:0004180" + ], + "obsolete abnormality of the epiphysis of the terminal phalanx of the middle finger": [ + "HP:0004183" + ], + "obsolete abnormality of the epiphyses of the terminal phalanx of the middle finger": [ + "HP:0004183" + ], + "obsolete cone - shaped epiphysis of terminal phalanx of the middle finger": [ + "HP:0004184" + ], + "obsolete fuse epiphysis of terminal phalanx of the middle finger": [ + "HP:0004185" + ], + "obsolete fused epiphysis of terminal phalanx of the middle finger": [ + "HP:0004185" + ], + "obsolete large epiphysis of terminal phalanx of the middle finger": [ + "HP:0004186" + ], + "obsolete prematurely fused epiphysis of terminal phalanx of the middle finger": [ + "HP:0004187" + ], + "abnormal 4th finger morphology": [ + "HP:0004188" + ], + "abnormality of the 4th finger": [ + "HP:0004188" + ], + "abnormality of the ring finger": [ + "HP:0004188" + ], + "obsolete bracket epiphysis of the 4th finger": [ + "HP:0004192" + ], + "obsolete bracket epiphyses of the 4th finger": [ + "HP:0004192" + ], + "obsolete expand phalanx of the ring finger": [ + "HP:0004193" + ], + "obsolete expanded phalanges of the ring finger": [ + "HP:0004193" + ], + "obsolete hypoplastic phalanx of the ring finger": [ + "HP:0004194" + ], + "obsolete hypoplastic phalanges of the ring finger": [ + "HP:0004194" + ], + "osteolytic defect of the phalanx of the 4th finger": [ + "HP:0004195" + ], + "osteolytic defects of the phalanges of the 4th finger": [ + "HP:0004195" + ], + "lytic defect of the phalanx of the ring finger": [ + "HP:0004195" + ], + "lytic defects of the phalanges of the ring finger": [ + "HP:0004195" + ], + "obsolete short phalanx of the ring finger": [ + "HP:0004196" + ], + "obsolete short phalanges of the ring finger": [ + "HP:0004196" + ], + "symphalangism of the 4th finger": [ + "HP:0004197" + ], + "fuse ring finger bone": [ + "HP:0004197" + ], + "fused ring finger bones": [ + "HP:0004197" + ], + "symphalangism of the ring finger": [ + "HP:0004197" + ], + "obsolete wide / broad phalanx of the ring finger": [ + "HP:0004198" + ], + "obsolete wide / broad phalanges of the ring finger": [ + "HP:0004198" + ], + "obsolete expand proximal phalanx of the ring finger": [ + "HP:0004201" + ], + "obsolete expanded proximal phalanx of the ring finger": [ + "HP:0004201" + ], + "obsolete lytic defect of the proximal phalanx of the ring finger": [ + "HP:0004202" + ], + "obsolete lytic defects of the proximal phalanx of the ring finger": [ + "HP:0004202" + ], + "obsolete short proximal phalanx of the ring finger": [ + "HP:0004203" + ], + "abnormal 5th finger morphology": [ + "HP:0004207" + ], + "abnormality of the 5th finger": [ + "HP:0004207" + ], + "abnormality of the little finger": [ + "HP:0004207" + ], + "abnormality of the pinkie finger": [ + "HP:0004207" + ], + "abnormality of the pinky finger": [ + "HP:0004207" + ], + "clinodactyly of the 5th finger": [ + "HP:0004209" + ], + "bilateral fifth digit clinodactyly": [ + "HP:0004209" + ], + "bilateral fifth finger clinodactyly": [ + "HP:0004209" + ], + "clinodactyly of fifth digit": [ + "HP:0004209" + ], + "clinodactyly of the little finger": [ + "HP:0004209" + ], + "curvature of little finger": [ + "HP:0004209" + ], + "curvature of pinkie finger": [ + "HP:0004209" + ], + "curvature of pinky finger": [ + "HP:0004209" + ], + "fifth finger clinodactyly": [ + "HP:0004209" + ], + "permanent curving of the pinkie finger": [ + "HP:0004209" + ], + "abnormal 5th finger phalanx morphology": [ + "HP:0004213" + ], + "abnormality of the little finger bone": [ + "HP:0004213" + ], + "abnormality of the phalanx of the 5th finger": [ + "HP:0004213" + ], + "abnormality of the phalanges of the 5th finger": [ + "HP:0004213" + ], + "abnormality of the pinkie finger bone": [ + "HP:0004213" + ], + "abnormality of the pinky finger bone": [ + "HP:0004213" + ], + "curve phalanx of the 5th finger": [ + "HP:0004214" + ], + "curved phalanges of the 5th finger": [ + "HP:0004214" + ], + "curve little finger bone": [ + "HP:0004214" + ], + "curved little finger bone": [ + "HP:0004214" + ], + "curve pinkie finger bone": [ + "HP:0004214" + ], + "curved pinkie finger bone": [ + "HP:0004214" + ], + "curve pinky finger bone": [ + "HP:0004214" + ], + "curved pinky finger bone": [ + "HP:0004214" + ], + "osteolytic defect of the phalanx of the 5th finger": [ + "HP:0004216" + ], + "osteolytic defects of the phalanges of the 5th finger": [ + "HP:0004216" + ], + "lytic defect of the phalanx of the little finger": [ + "HP:0004216" + ], + "lytic defects of the phalanges of the little finger": [ + "HP:0004216" + ], + "symphalangism of the 5th finger": [ + "HP:0004218" + ], + "fifth finger symphalangism": [ + "HP:0004218" + ], + "fuse little finger bone": [ + "HP:0004218" + ], + "fused little finger bones": [ + "HP:0004218" + ], + "fuse pinkie finger bone": [ + "HP:0004218" + ], + "fused pinkie finger bones": [ + "HP:0004218" + ], + "fuse pinky finger bone": [ + "HP:0004218" + ], + "fused pinky finger bones": [ + "HP:0004218" + ], + "symphalagism of the little finger": [ + "HP:0004218" + ], + "abnormality of the middle phalanx of the 5th finger": [ + "HP:0004219" + ], + "abnormality of the middle bone of little finger": [ + "HP:0004219" + ], + "abnormality of the middle bone of pinkie finger": [ + "HP:0004219" + ], + "abnormality of the middle bone of pinky finger": [ + "HP:0004219" + ], + "short middle phalanx of the 5th finger": [ + "HP:0004220" + ], + "5th finger middle phalangeal hypoplasia": [ + "HP:0004220" + ], + "brachymesophalangism v": [ + "HP:0004220" + ], + "brachymesophalangy v ( finger )": [ + "HP:0004220" + ], + "fifth finger mid - phalanx hypoplasia": [ + "HP:0004220" + ], + "hypoplastic fifth finger middle phalanx": [ + "HP:0004220" + ], + "hypoplastic middle phalanx of the 5th finger": [ + "HP:0004220" + ], + "hypoplastic / small middle phalanx of the 5th finger": [ + "HP:0004220" + ], + "hypoplastic / small middle phalanx of the little finger": [ + "HP:0004220" + ], + "short middle bone of the little finger": [ + "HP:0004220" + ], + "short middle bone of the pinkie finger": [ + "HP:0004220" + ], + "short middle bone of the pinky finger": [ + "HP:0004220" + ], + "short middle phalanx of the little finger": [ + "HP:0004220" + ], + "type a3 brachydactyly": [ + "HP:0004220" + ], + "cone - shaped epiphysis of the distal phalanx of the 5th finger": [ + "HP:0004222" + ], + "cone - shaped end part of the outermost little finger bone": [ + "HP:0004222" + ], + "cone - shaped end part of the outermost pinkie finger bone": [ + "HP:0004222" + ], + "cone - shaped end part of the outermost pinky finger bone": [ + "HP:0004222" + ], + "cone - shaped epiphysis of the distal phalanx of the little finger": [ + "HP:0004222" + ], + "ivory epiphysis of the distal phalanx of the 5th finger": [ + "HP:0004223" + ], + "increase bone density of end part of the outermost little finger bone": [ + "HP:0004223" + ], + "increased bone density of end part of the outermost little finger bone": [ + "HP:0004223" + ], + "increase bone density of end part of the outermost pinkie finger bone": [ + "HP:0004223" + ], + "increased bone density of end part of the outermost pinkie finger bone": [ + "HP:0004223" + ], + "increase bone density of end part of the outermost pinky finger bone": [ + "HP:0004223" + ], + "increased bone density of end part of the outermost pinky finger bone": [ + "HP:0004223" + ], + "ivory epiphysis of the distal phalanx of the little finger": [ + "HP:0004223" + ], + "ivory epiphysis of the terminal phalanx of the little finger": [ + "HP:0004223" + ], + "abnormality of the epiphysis of the middle phalanx of the 5th finger": [ + "HP:0004224" + ], + "abnormality of the end part of middle little finger bone": [ + "HP:0004224" + ], + "abnormality of the end part of middle pinkie finger bone": [ + "HP:0004224" + ], + "abnormality of the end part of middle pinky finger bone": [ + "HP:0004224" + ], + "abnormality of the distal phalanx of the 5th finger": [ + "HP:0004225" + ], + "abnormality of the distal phalanx of the little finger": [ + "HP:0004225" + ], + "abnormality of the outermost little finger bone": [ + "HP:0004225" + ], + "abnormality of the outermost pinkie finger bone": [ + "HP:0004225" + ], + "abnormality of the outermost pinky finger bone": [ + "HP:0004225" + ], + "abnormality of the terminal phalanx of the little finger": [ + "HP:0004225" + ], + "curve distal phalanx of the 5th finger": [ + "HP:0004226" + ], + "curved distal phalanx of the 5th finger": [ + "HP:0004226" + ], + "curve outermost little finger bone": [ + "HP:0004226" + ], + "curved outermost little finger bone": [ + "HP:0004226" + ], + "curve outermost pinkie finger bone": [ + "HP:0004226" + ], + "curved outermost pinkie finger bone": [ + "HP:0004226" + ], + "curve outermost pinky finger bone": [ + "HP:0004226" + ], + "curved outermost pinky finger bone": [ + "HP:0004226" + ], + "curve terminal phalanx of the little finger": [ + "HP:0004226" + ], + "curved terminal phalanx of the little finger": [ + "HP:0004226" + ], + "short distal phalanx of the 5th finger": [ + "HP:0004227" + ], + "brachytelophalangism v": [ + "HP:0004227" + ], + "fifth digit distal phalangeal hypoplasia": [ + "HP:0004227" + ], + "hypoplastic / small terminal phalanx of the little finger": [ + "HP:0004227" + ], + "short distal phalanx of the fifth finger": [ + "HP:0004227" + ], + "short outermost little finger bone": [ + "HP:0004227" + ], + "short outermost pinkie finger bone": [ + "HP:0004227" + ], + "short outermost pinky finger bone": [ + "HP:0004227" + ], + "subluxation of the proximal interphalangeal joint of the little finger": [ + "HP:0004230" + ], + "partially dislocate innermost hinge joint of little finger": [ + "HP:0004230" + ], + "partially dislocated innermost hinge joint of little finger": [ + "HP:0004230" + ], + "partially dislocate innermost hinge joint of pinkie finger": [ + "HP:0004230" + ], + "partially dislocated innermost hinge joint of pinkie finger": [ + "HP:0004230" + ], + "partially dislocate innermost hinge joint of pinky finger": [ + "HP:0004230" + ], + "partially dislocated innermost hinge joint of pinky finger": [ + "HP:0004230" + ], + "carpal bone aplasia": [ + "HP:0004231" + ], + "absent carpal bone": [ + "HP:0004231" + ], + "absent carpal bones": [ + "HP:0004231" + ], + "absent carpal ossification center": [ + "HP:0004231" + ], + "absent carpal ossification centre": [ + "HP:0004231" + ], + "absent wrist bone": [ + "HP:0004231" + ], + "aplastic carpal bone": [ + "HP:0004231" + ], + "miss wrist bone": [ + "HP:0004231" + ], + "missing wrist bone": [ + "HP:0004231" + ], + "accessory carpal bone": [ + "HP:0004232" + ], + "accessory carpal bones": [ + "HP:0004232" + ], + "extra wrist bone": [ + "HP:0004232" + ], + "extra wrist bones": [ + "HP:0004232" + ], + "supernumerary carpal bone": [ + "HP:0004232" + ], + "supernumerary carpal bones": [ + "HP:0004232" + ], + "advanced ossification of carpal bone": [ + "HP:0004233" + ], + "advanced ossification of carpal bones": [ + "HP:0004233" + ], + "accelerate carpal bone maturation": [ + "HP:0004233" + ], + "accelerated carpal bone maturation": [ + "HP:0004233" + ], + "accelerate wrist bone maturation": [ + "HP:0004233" + ], + "accelerated wrist bone maturation": [ + "HP:0004233" + ], + "advanced carpal bone age": [ + "HP:0004233" + ], + "advanced carpal ossification": [ + "HP:0004233" + ], + "precociously ossify carpal bone": [ + "HP:0004233" + ], + "precociously ossified carpal bones": [ + "HP:0004233" + ], + "bone - in - a - bone appearance of carpal bone": [ + "HP:0004234" + ], + "bone - in - a - bone appearance of carpal bones": [ + "HP:0004234" + ], + "bone - in - a - bone appearance of wrist bone": [ + "HP:0004234" + ], + "bone - in - a - bone appearance of wrist bones": [ + "HP:0004234" + ], + "comma - shape carpal bone": [ + "HP:0004235" + ], + "comma - shaped carpal bones": [ + "HP:0004235" + ], + "comma - shaped wrist bone": [ + "HP:0004235" + ], + "comma - shaped wrist bones": [ + "HP:0004235" + ], + "irregular carpal bone": [ + "HP:0004236" + ], + "irregular carpal bones": [ + "HP:0004236" + ], + "irregular wrist bone": [ + "HP:0004236" + ], + "irregular wrist bones": [ + "HP:0004236" + ], + "large carpal bone": [ + "HP:0004237" + ], + "large carpal bones": [ + "HP:0004237" + ], + "large carpal": [ + "HP:0004237" + ], + "large carpals": [ + "HP:0004237" + ], + "large wrist bone": [ + "HP:0004237" + ], + "large wrist bones": [ + "HP:0004237" + ], + "lytic defect of carpal bone": [ + "HP:0004238" + ], + "lytic defects of carpal bones": [ + "HP:0004238" + ], + "proximally place carpal bone": [ + "HP:0004239" + ], + "proximally placed carpal bones": [ + "HP:0004239" + ], + "sclerotic focus within carpal bone": [ + "HP:0004240" + ], + "sclerotic foci within carpal bones": [ + "HP:0004240" + ], + "harden spot within wrist bone": [ + "HP:0004240" + ], + "hardened spots within wrist bones": [ + "HP:0004240" + ], + "stiffen spot within wrist bone": [ + "HP:0004240" + ], + "stiffened spots within wrist bones": [ + "HP:0004240" + ], + "stipple calcification in carpal bone": [ + "HP:0004241" + ], + "stippled calcification in carpal bones": [ + "HP:0004241" + ], + "punctate calcification of carpal": [ + "HP:0004241" + ], + "punctate calcifications of carpals": [ + "HP:0004241" + ], + "broad carpal bone": [ + "HP:0004242" + ], + "broad carpal bones": [ + "HP:0004242" + ], + "wide carpal bone": [ + "HP:0004242" + ], + "wide carpal bones": [ + "HP:0004242" + ], + "wide wrist bone": [ + "HP:0004242" + ], + "wide wrist bones": [ + "HP:0004242" + ], + "abnormality of the scaphoid": [ + "HP:0004243" + ], + "accessory scaphoid": [ + "HP:0004244" + ], + "comma - shape scaphoid": [ + "HP:0004245" + ], + "comma - shaped scaphoid": [ + "HP:0004245" + ], + "delay ossification of the scaphoid": [ + "HP:0004246" + ], + "delayed ossification of the scaphoid": [ + "HP:0004246" + ], + "delay maturation of the scaphoid": [ + "HP:0004246" + ], + "delayed maturation of the scaphoid": [ + "HP:0004246" 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], + "delay maturation of the trapezoid bone": [ + "HP:0004257" + ], + "delayed maturation of the trapezoid bone": [ + "HP:0004257" + ], + "small trapezoid bone": [ + "HP:0004258" + ], + "abnormality of the hamate bone": [ + "HP:0004259" + ], + "large hamate bone": [ + "HP:0004260" + ], + "large unciform bone": [ + "HP:0004260" + ], + "wide hamate bone": [ + "HP:0004261" + ], + "broad hamate bone": [ + "HP:0004261" + ], + "wide unciform bone": [ + "HP:0004261" + ], + "abnormality of the capitate bone": [ + "HP:0004262" + ], + "large capitate bone": [ + "HP:0004263" + ], + "narrow carpal joint space": [ + "HP:0004264" + ], + "narrow carpal joint spaces": [ + "HP:0004264" + ], + "decrease carpal joint angle": [ + "HP:0004264" + ], + "decreased carpal joint angles": [ + "HP:0004264" + ], + "narrow small joint of the hand": [ + "HP:0004267" + ], + "narrow small joints of the hand": [ + "HP:0004267" + ], + "osteoarthritis of the small joint of the hand": [ + "HP:0004268" + ], + "osteoarthritis of the small joints of the hand": [ + "HP:0004268" + ], + "subluxation of the small joint of the hand": [ + "HP:0004269" + ], + "subluxation of the small joints of the hand": [ + "HP:0004269" + ], + "partial dislocation of small joint of hand": [ + "HP:0004269" + ], + "partial dislocation of small joints of hand": [ + "HP:0004269" + ], + "cortical thickening of hand bone": [ + "HP:0004271" + ], + "cortical thickening of hand bones": [ + "HP:0004271" + ], + "cortical thinning of hand bone": [ + "HP:0004272" + ], + "cortical thinning of hand bones": [ + "HP:0004272" + ], + "cupped metaphyses of hand bone": [ + "HP:0004273" + ], + "cupped metaphyses of hand bones": [ + "HP:0004273" + ], + "cupped metaphysis of hand bone": [ + "HP:0004273" + ], + "cupped metaphysis of hand bones": [ + "HP:0004273" + ], + "cup wide portion of hand bone": [ + "HP:0004273" + ], + "cupped wide portion of hand bones": [ + "HP:0004273" + ], + "deficient ossification of hand bone": [ + "HP:0004274" + ], + "deficient ossification of hand bones": [ + "HP:0004274" + ], + "deficient maturation of hand bone": [ + "HP:0004274" + ], + "deficient maturation of hand bones": [ + "HP:0004274" + ], + "duplication of hand bone": [ + "HP:0004275" + ], + "duplication of hand bones": [ + "HP:0004275" + ], + "exostosis of hand bone": [ + "HP:0004276" + ], + "exostoses of hand bones": [ + "HP:0004276" + ], + "fractured hand bone": [ + "HP:0004277" + ], + "fractured hand bones": [ + "HP:0004277" + ], + "broken hand bone": [ + "HP:0004277" + ], + "broken hand bones": [ + "HP:0004277" + ], + "synostosis involve bone of the hand": [ + "HP:0004278" + ], + "synostosis involving bones of the hand": [ + "HP:0004278" + ], + "fused hand bone": [ + "HP:0004278" + ], + "fused hand bones": [ + "HP:0004278" + ], + "short palm": [ + "HP:0004279" + ], + "hypoplastic hand": [ + "HP:0004279" + ], + "hypoplastic hands": [ + "HP:0004279" + ], + "short hand": [ + "HP:0004279" + ], + "short hands": [ + "HP:0004279" + ], + "short palms": [ + "HP:0004279" + ], + "irregular ossification of hand bone": [ + "HP:0004280" + ], + "irregular ossification of hand bones": [ + "HP:0004280" + ], + "irregular maturation of hand bone": [ + "HP:0004280" + ], + "irregular maturation of hand bones": [ + "HP:0004280" + ], + "irregular sclerosis of hand bone": [ + "HP:0004281" + ], + "irregular sclerosis of hand bones": [ + "HP:0004281" + ], + "narrow palm": [ + "HP:0004283" + ], + "narrow hand": [ + "HP:0004283" + ], + "narrow hands": [ + "HP:0004283" + ], + "notched hand bone": [ + "HP:0004284" + ], + "notched hand bones": [ + "HP:0004284" + ], + "overmodelled hand bone": [ + "HP:0004285" + ], + "overmodelled hand bones": [ + "HP:0004285" + ], + "patchy sclerosis of hand bone": [ + "HP:0004286" + ], + "patchy sclerosis of hand bones": [ + "HP:0004286" + ], + "uneven increase in bone density in hand bone": [ + "HP:0004286" + ], + "uneven increase in bone density in hand bones": [ + "HP:0004286" + ], + "point hand bone": [ + "HP:0004287" + ], + "pointed hand bones": [ + "HP:0004287" + ], + "pseudoepiphyses of hand bone": [ + "HP:0004288" + ], + "pseudoepiphyses of hand bones": [ + "HP:0004288" + ], + "sclerotic focus in hand bone": [ + "HP:0004289" + ], + "sclerotic foci in hand bones": [ + "HP:0004289" + ], + "sclerosis of hand bone with transverse striation": [ + "HP:0004290" + ], + "sclerosis of hand bones with transverse striations": [ + "HP:0004290" + ], + "stipple calcification of hand bone": [ + "HP:0004291" + ], + "stippled calcification of hand bones": [ + "HP:0004291" + ], + "undermodelled hand bone": [ + "HP:0004292" + ], + "undermodelled hand bones": [ + "HP:0004292" + ], + "synostosis of second metacarpal - trapezoid": [ + "HP:0004293" + ], + "fusion of second metacarpal - trapezoid": [ + "HP:0004293" + ], + "subluxation of metacarpal phalangeal joint": [ + "HP:0004294" + ], + "subluxation of metacarpal phalangeal joints": [ + "HP:0004294" + ], + "partial knuckle dislocation": [ + "HP:0004294" + ], + "subluxation of metacarpophalangeal joint": [ + "HP:0004294" + ], + "subluxation of metacarpophalangeal joints": [ + "HP:0004294" + ], + "abnormality of the gastric mucosa": [ + "HP:0004295" + ], + "abnormality of the mucous membrane layer of stomach": [ + "HP:0004295" + ], + "abnormality of gastrointestinal vasculature": [ + "HP:0004296" + ], + "abnormality of gi blood vessel": [ + "HP:0004296" + ], + "abnormality of gi blood vessels": [ + "HP:0004296" + ], + "abnormality of gi vasculature": [ + "HP:0004296" + ], + "abnormality of the biliary system": [ + "HP:0004297" + ], + "abnormality of the abdominal wall": [ + "HP:0004298" + ], + "abnormality of external feature of the abdomen": [ + "HP:0004298" + ], + "abnormality of external features of the abdomen": [ + "HP:0004298" + ], + "hernia of the abdominal wall": [ + "HP:0004299" + ], + "herniated abdominal wall": [ + "HP:0004299" + ], + "functional motor deficit": [ + "HP:0004302" + ], + "functional motor problem": [ + "HP:0004302" + ], + "functional motor problems": [ + "HP:0004302" + ], + "abnormal muscle fiber morphology": [ + "HP:0004303" + ], + "abnormal muscle fibre morphology": [ + "HP:0004303" + ], + "abnormal skeletal muscle fiber morphology": [ + "HP:0004303" + ], + "abnormal skeletal muscle fibre morphology": [ + "HP:0004303" + ], + "abnormality of muscle fiber": [ + "HP:0004303" + ], + "abnormality of muscle fibers": [ + "HP:0004303" + ], + "abnormality of muscle fibre": [ + "HP:0004303" + ], + "abnormality of muscle fibres": [ + "HP:0004303" + ], + "involuntary movement": [ + "HP:0004305" + ], + "involuntary movements": [ + "HP:0004305" + ], + "involuntary muscle contraction": [ + "HP:0004305" + ], + "involuntary muscle contractions": [ + "HP:0004305" + ], + "abnormal endocardium morphology": [ + "HP:0004306" + ], + "abnormality of the endocardium": [ + "HP:0004306" + ], + "abnormality of the endomycoardium": [ + "HP:0004306" + ], + "abnormal anatomic location of the heart": [ + "HP:0004307" + ], + "ventricular arrhythmia": [ + "HP:0004308" + ], + "ventricular arrhythmias": [ + "HP:0004308" + ], + "ventricular preexcitation": [ + "HP:0004309" + ], + "pre - excitation syndrome": [ + "HP:0004309" + ], + "preexcitation": [ + "HP:0004309" + ], + "ventricular pre - excitation": [ + "HP:0004309" + ], + "abnormal macrophage morphology": [ + "HP:0004311" + ], + "abnormality of histiocyte": [ + "HP:0004311" + ], + "abnormality of histiocytes": [ + "HP:0004311" + ], + "abnormality of macrophage": [ + "HP:0004311" + ], + "abnormality of macrophages": [ + "HP:0004311" + ], + "abnormal reticulocyte morphology": [ + "HP:0004312" + ], + "abnormality of reticulocyte": [ + "HP:0004312" + ], + "abnormality of reticulocytes": [ + "HP:0004312" + ], + "decrease circulate antibody level": [ + "HP:0004313" + ], + "decreased circulating antibody level": [ + "HP:0004313" + ], + "decrease antibody level in blood": [ + "HP:0004313" + ], + "decreased antibody level in blood": [ + "HP:0004313" + ], + "decrease immunoglobulin level": [ + "HP:0004313" + ], + "decreased immunoglobulin level": [ + "HP:0004313" + ], + "decrease serum immunoglobulin": [ + "HP:0004313" + ], + "decreased serum immunoglobulin": [ + "HP:0004313" + ], + "hypogammaglobulinemia": [ + "HP:0004313" + ], + "immunoglobulin deficiency": [ + "HP:0004313" + ], + "reduce immunoglobulin level": [ + "HP:0004313" + ], + "reduced immunoglobulin levels": [ + "HP:0004313" + ], + "decrease circulate igg level": [ + "HP:0004315" + ], + "decreased circulating igg level": [ + "HP:0004315" + ], + "decrease gamma - globin expression": [ + "HP:0004315" + ], + "decreased gamma - globin expression": [ + "HP:0004315" + ], + "decrease igg level": [ + "HP:0004315" + ], + "decreased igg level": [ + "HP:0004315" + ], + "decrease igg level in blood": [ + "HP:0004315" + ], + "decreased igg level in blood": [ + "HP:0004315" + ], + "decrease immunoglobulin g": [ + "HP:0004315" + ], + "decreased immunoglobulin g": [ + "HP:0004315" + ], + "decrease serum igg": [ + "HP:0004315" + ], + "decreased serum igg": [ + "HP:0004315" + ], + "igg deficiency": [ + "HP:0004315" + ], + "reduce igg level": [ + "HP:0004315" + ], + "reduced igg levels": [ + "HP:0004315" + ], + "decrease circulate aldosterone level": [ + "HP:0004319" + ], + "decreased circulating aldosterone level": [ + "HP:0004319" + ], + "decrease aldosterone": [ + "HP:0004319" + ], + "decreased aldosterone": [ + "HP:0004319" + ], + "decrease aldosterone production": [ + "HP:0004319" + ], + "decreased aldosterone production": [ + "HP:0004319" + ], + "decrease serum aldosterone": [ + "HP:0004319" + ], + "decreased serum aldosterone": [ + "HP:0004319" + ], + "hypoaldosteronism": [ + "HP:0004319" + ], + "low blood aldosterone level": [ + "HP:0004319" + ], + "mineralocorticoid insufficiency": [ + "HP:0004319" + ], + "vaginal fistula": [ + "HP:0004320" + ], + "bladder fistula": [ + "HP:0004321" + ], + "short stature": [ + "HP:0004322" + ], + "decrease body height": [ + "HP:0004322" + ], + "decreased body height": [ + "HP:0004322" + ], + "height less than 3rd percentile": [ + "HP:0004322" + ], + "small stature": [ + "HP:0004322" + ], + "stature below 3rd percentile": [ + "HP:0004322" + ], + "abnormality of body weight": [ + "HP:0004323" + ], + "abnormality of habitus": [ + "HP:0004323" + ], + "increase body weight": [ + "HP:0004324" + ], + "increased body weight": [ + "HP:0004324" + ], + "weight gain": [ + "HP:0004324" + ], + "decrease body weight": [ + "HP:0004325" + ], + "decreased body weight": [ + "HP:0004325" + ], + "decrease weight": [ + "HP:0004325" + ], + "decreased weight": [ + "HP:0004325" + ], + "low body weight": [ + "HP:0004325" + ], + "low weight": [ + "HP:0004325" + ], + "weight less than 3rd percentile": [ + "HP:0004325" + ], + "cachexia": [ + "HP:0004326" + ], + "waste syndrome": [ + "HP:0004326" + ], + "wasting syndrome": [ + "HP:0004326" + ], + "abnormal vitreous humor morphology": [ + "HP:0004327" + ], + "abnormal vitreous humour morphology": [ + "HP:0004327" + ], + "abnormal anterior eye segment morphology": [ + "HP:0004328" + ], + "abnormal anterior segment morphology": [ + "HP:0004328" + ], + "abnormality of the anterior segment of the eye": [ + "HP:0004328" + ], + "abnormality of the anterior segment of the eyeball": [ + "HP:0004328" + ], + "abnormality of the anterior segment of the globe": [ + "HP:0004328" + ], + "abnormal posterior eye segment morphology": [ + "HP:0004329" + ], + "abnormal morphology of the posterior segment of the globe": [ + "HP:0004329" + ], + "abnormality of the posterior segment of the eye": [ + "HP:0004329" + ], + "abnormality of the posterior segment of the eyeball": [ + "HP:0004329" + ], + "abnormality of the posterior segment of the globe": [ + "HP:0004329" + ], + "increase skull ossification": [ + "HP:0004330" + ], + "increased skull ossification": [ + "HP:0004330" + ], + "hyperossification of skull": [ + "HP:0004330" + ], + "hyperostosis of skull": [ + "HP:0004330" + ], + "increase calcification of skull": [ + "HP:0004330" + ], + "increased calcification of skull": [ + "HP:0004330" + ], + "increase mineralization of skull": [ + "HP:0004330" + ], + "increased mineralization of skull": [ + "HP:0004330" + ], + "sclerosis of bone of skull": [ + "HP:0004330" + ], + "sclerosis of bones of skull": [ + "HP:0004330" + ], + "sclerosis of skull": [ + "HP:0004330" + ], + "decrease skull ossification": [ + "HP:0004331" + ], + "decreased skull ossification": [ + "HP:0004331" + ], + "decrease bone formation of skull": [ + "HP:0004331" + ], + "decreased bone formation of skull": [ + "HP:0004331" + ], + "decreased calcification of skull": [ + "HP:0004331" + ], + "decreased mineralization of skull": [ + "HP:0004331" + ], + "deficient skull ossification": [ + "HP:0004331" + ], + "hypoossification of skull": [ + "HP:0004331" + ], + "ossification defect of skull": [ + "HP:0004331" + ], + "poorly mineralize skull": [ + "HP:0004331" + ], + "poorly mineralized skull": [ + "HP:0004331" + ], + "poorly ossify skull": [ + "HP:0004331" + ], + "poorly ossified skull": [ + "HP:0004331" + ], + "poorly ossify skull bone": [ + "HP:0004331" + ], + "poorly ossified skull bones": [ + "HP:0004331" + ], + "abnormal lymphocyte morphology": [ + "HP:0004332" + ], + "abnormal lymphocyte": [ + "HP:0004332" + ], + "abnormal lymphocytes": [ + "HP:0004332" + ], + "abnormality of cell of the lymphoid lineage": [ + "HP:0004332" + ], + "abnormality of cells of the lymphoid lineage": [ + "HP:0004332" + ], + "bone - marrow foam cell": [ + "HP:0004333" + ], + "bone - marrow foam cells": [ + "HP:0004333" + ], + "bone marrow foam cell": [ + "HP:0004333" + ], + "bone marrow foam cells": [ + "HP:0004333" + ], + "large vacuolated foam cell ( 'np cell ' ) on bone marrow biopsy": [ + "HP:0004333" + ], + "large vacuolated foam cells ( 'np cells ' ) on bone marrow biopsy": [ + "HP:0004333" + ], + "large vacuolated foam cell on bone marrow biopsy": [ + "HP:0004333" + ], + "large vacuolated foam cells on bone marrow biopsy": [ + "HP:0004333" + ], + "dermal atrophy": [ + "HP:0004334" + ], + "atrophic skin": [ + "HP:0004334" + ], + "skin atrophy": [ + "HP:0004334" + ], + "skin degeneration": [ + "HP:0004334" + ], + "myelin outfoldings": [ + "HP:0004336" + ], + "excessive focal folding of myelin sheath": [ + "HP:0004336" + ], + "excessive focal folding of myelin sheaths": [ + "HP:0004336" + ], + "irregular myelin folding": [ + "HP:0004336" + ], + "irregular myelin foldings": [ + "HP:0004336" + ], + "abnormality of amino acid metabolism": [ + "HP:0004337" + ], + "amino acid level abnormal": [ + "HP:0004337" + ], + "amino acid levels abnormal": [ + "HP:0004337" + ], + "abnormal circulate aromatic amino acid concentration": [ + "HP:0004338" + ], + "abnormal circulating aromatic amino acid concentration": [ + "HP:0004338" + ], + "abnormality of aromatic amino acid family metabolism": [ + "HP:0004338" + ], + "abnormal circulate sulfur amino acid concentration": [ + "HP:0004339" + ], + "abnormal circulating sulfur amino acid concentration": [ + "HP:0004339" + ], + "abnormal circulate sulphur amino acid concentration": [ + "HP:0004339" + ], + "abnormal circulating sulphur amino acid concentration": [ + "HP:0004339" + ], + "abnormality of sulfur - contain amino acid": [ + "HP:0004339" + ], + "abnormality of sulfur - containing amino acids": [ + "HP:0004339" + ], + "abnormality of vitamin b metabolism": [ + "HP:0004340" + ], + "abnormality of b - vitamin metabolism": [ + "HP:0004340" + ], + "abnormality of vitamin b12 metabolism": [ + "HP:0004341" + ], + "abnormality of the vitamin b12 metabolism": [ + "HP:0004341" + ], + "abnormality of galactoside metabolism": [ + "HP:0004342" + ], + "abnormal glycosphingolipid metabolism": [ + "HP:0004343" + ], + "abnormality of glycosphingolipid metabolism": [ + "HP:0004343" + ], + "abnormality of cerebrosidase metabolism": [ + "HP:0004344" + ], + "ganglioside accumulation": [ + "HP:0004345" + ], + "weakness of muscle of respiration": [ + "HP:0004347" + ], + "weakness of muscles of respiration": [ + "HP:0004347" + ], + "abnormality of bone mineral density": [ + "HP:0004348" + ], + "abnormality of bone mineralisation and ossification": [ + "HP:0004348" + ], + "reduce bone mineral density": [ + "HP:0004349" + ], + "reduced bone mineral density": [ + "HP:0004349" + ], + "decrease bone mineral density": [ + "HP:0004349" + ], + "decreased bone mineral density": [ + "HP:0004349" + ], + "decrease bone mineral density z score": [ + "HP:0004349" + ], + "decreased bone mineral density z score": [ + "HP:0004349" + ], + "low solidness and mass of the bone": [ + "HP:0004349" + ], + "low solidness and mass of the bones": [ + "HP:0004349" + ], + "abnormal circulate purine concentration": [ + "HP:0004352" + ], + "abnormal circulating purine concentration": [ + "HP:0004352" + ], + "abnormal circulate purine level": [ + "HP:0004352" + ], + "abnormal circulating purine level": [ + "HP:0004352" + ], + "abnormal circulate pyrimidine concentration": [ + "HP:0004353" + ], + "abnormal circulating pyrimidine concentration": [ + "HP:0004353" + ], + "abnormal circulate carboxylic acid concentration": [ + "HP:0004354" + ], + "abnormal circulating carboxylic acid concentration": [ + "HP:0004354" + ], + "obsolete abnormality of proteoglycan metabolism": [ + "HP:0004355" + ], + "abnormality of lysosomal metabolism": [ + "HP:0004356" + ], + "abnormal circulate leucine concentration": [ + "HP:0004357" + ], + "abnormal circulating leucine concentration": [ + "HP:0004357" + ], + "abnormality of superoxide metabolism": [ + "HP:0004358" + ], + "abnormal circulate fatty - acid concentration": [ + "HP:0004359" + ], + "abnormal circulating fatty - acid concentration": [ + "HP:0004359" + ], + "abnormality of fatty acid metabolism": [ + "HP:0004359" + ], + "fatty acid abnormal": [ + "HP:0004359" + ], + "fatty acids abnormal": [ + "HP:0004359" + ], + "abnormality of acid - base homeostasis": [ + "HP:0004360" + ], + "acid base imbalance": [ + "HP:0004360" + ], + "abnormality of circulate leptin level": [ + "HP:0004361" + ], + "abnormality of circulating leptin level": [ + "HP:0004361" + ], + "abnormality of enteric ganglion morphology": [ + "HP:0004362" + ], + "abnormality of the enteric ganglion": [ + "HP:0004362" + ], + "abnormality of the enteric ganglia": [ + "HP:0004362" + ], + "abnormal circulate calcium concentration": [ + "HP:0004363" + ], + "abnormal circulating calcium concentration": [ + "HP:0004363" + ], + "abnormal blood calcium concentration": [ + "HP:0004363" + ], + "abnormal blood calcium level": [ + "HP:0004363" + ], + "abnormal blood calcium levels": [ + "HP:0004363" + ], + "abnormal circulate ca concentration": [ + "HP:0004363" + ], + "abnormal circulating ca concentration": [ + "HP:0004363" + ], + "abnormal circulate ca2+ concentration": [ + "HP:0004363" + ], + "abnormal circulating ca2+ concentration": [ + "HP:0004363" + ], + "abnormal circulate nitrogen compound concentration": [ + "HP:0004364" + ], + "abnormal circulating nitrogen compound concentration": [ + "HP:0004364" + ], + "abnormal circulate tryptophan concentration": [ + "HP:0004365" + ], + "abnormal circulating tryptophan concentration": [ + "HP:0004365" + ], + "abnormality of tryptophan metabolism": [ + "HP:0004365" + ], + "abnormality of glycolysis": [ + "HP:0004366" + ], + "obsolete abnormality of glycoprotein metabolism": [ + "HP:0004367" + ], + "increase circulate purine concentration": [ + "HP:0004368" + ], + "increased circulating purine concentration": [ + "HP:0004368" + ], + "increase purine level": [ + "HP:0004368" + ], + "increased purine level": [ + "HP:0004368" + ], + "increased purine levels": [ + "HP:0004368" + ], + "decrease circulate purine concentration": [ + "HP:0004369" + ], + "decreased circulating purine concentration": [ + "HP:0004369" + ], + "decrease purine level": [ + "HP:0004369" + ], + "decreased purine level": [ + "HP:0004369" + ], + "decreased purine levels": [ + "HP:0004369" + ], + "abnormality of temperature regulation": [ + "HP:0004370" + ], + "body temperature change": [ + "HP:0004370" + ], + "body temperature changes": [ + "HP:0004370" + ], + "poor temperature regulation": [ + "HP:0004370" + ], + "abnormality of glycosaminoglycan metabolism": [ + "HP:0004371" + ], + "reduce consciousness / confusion": [ + "HP:0004372" + ], + "reduced consciousness / confusion": [ + "HP:0004372" + ], + "disturbance of consciousness": [ + "HP:0004372" + ], + "disturbances of consciousness": [ + "HP:0004372" + ], + "lower consciousness": [ + "HP:0004372" + ], + "lowered consciousness": [ + "HP:0004372" + ], + "focal dystonia": [ + "HP:0004373" + ], + "hemiplegia / hemiparesis": [ + "HP:0004374" + ], + "paralysis or weakness of one side of body": [ + "HP:0004374" + ], + "neoplasm of the nervous system": [ + "HP:0004375" + ], + "neoplasia of the nervous system": [ + "HP:0004375" + ], + "nervous system cancer": [ + "HP:0004375" + ], + "tumor of the nervous system": [ + "HP:0004375" + ], + "tumour of the nervous system": [ + "HP:0004375" + ], + "neuroblastic tumor": [ + "HP:0004376" + ], + "neuroblastic tumour": [ + "HP:0004376" + ], + "hematological neoplasm": [ + "HP:0004377" + ], + "blood tumor": [ + "HP:0004377" + ], + "blood tumour": [ + "HP:0004377" + ], + "haematological neoplasm": [ + "HP:0004377" + ], + "abnormality of the anus": [ + "HP:0004378" + ], + "abnormality of alkaline phosphatase level": [ + "HP:0004379" + ], + "abnormality of alkaline phosphatase activity": [ + "HP:0004379" + ], + "abnormality of alp level": [ + "HP:0004379" + ], + "alkaline phosphatase abnormal": [ + "HP:0004379" + ], + "aortic valve calcification": [ + "HP:0004380" + ], + "supravalvular aortic stenosis": [ + "HP:0004381" + ], + "mitral valve calcification": [ + "HP:0004382" + ], + "hypoplastic leave heart": [ + "HP:0004383" + ], + "hypoplastic left heart": [ + "HP:0004383" + ], + "heart leave ventricle hypoplasia": [ + "HP:0004383" + ], + "heart left ventricle hypoplasia": [ + "HP:0004383" + ], + "leave ventricular hypoplasia": [ + "HP:0004383" + ], + "left ventricular hypoplasia": [ + "HP:0004383" + ], + "underdeveloped leave heart": [ + "HP:0004383" + ], + "underdeveloped left heart": [ + "HP:0004383" + ], + "type i truncus arteriosus": [ + "HP:0004384" + ], + "persistent truncus arteriosus type i": [ + "HP:0004384" + ], + "type 1 truncus arteriosus": [ + "HP:0004384" + ], + "protract diarrhea": [ + "HP:0004385" + ], + "protracted diarrhea": [ + "HP:0004385" + ], + "protract diarrhoea": [ + "HP:0004385" + ], + "protracted diarrhoea": [ + "HP:0004385" + ], + "gastrointestinal inflammation": [ + "HP:0004386" + ], + "gi inflammation": [ + "HP:0004386" + ], + "enterocolitis": [ + "HP:0004387" + ], + "microcolon": [ + "HP:0004388" + ], + "microcolon on contrast enema": [ + "HP:0004388" + ], + "intestinal pseudo - obstruction": [ + "HP:0004389" + ], + "intestinal pseudoobstruction": [ + "HP:0004389" + ], + "hamartomatous polyposis": [ + "HP:0004390" + ], + "gastrointestinal hamartoma": [ + "HP:0004390" + ], + "gastrointestinal hamartomatous polyp": [ + "HP:0004390" + ], + "gastrointestinal hamartomatous polyps": [ + "HP:0004390" + ], + "hamartomatous polyp": [ + "HP:0004390" + ], + "hamartomatous polyps": [ + "HP:0004390" + ], + "prune belly": [ + "HP:0004392" + ], + "multiple gastric polyp": [ + "HP:0004394" + ], + "multiple gastric polyps": [ + "HP:0004394" + ], + "malnutrition": [ + "HP:0004395" + ], + "poor appetite": [ + "HP:0004396" + ], + "decrease appetite": [ + "HP:0004396" + ], + "decreased appetite": [ + "HP:0004396" + ], + "loss of appetite": [ + "HP:0004396" + ], + "no appetite": [ + "HP:0004396" + ], + "ectopic anus": [ + "HP:0004397" + ], + "abnormal anus position": [ + "HP:0004397" + ], + "anus malposition": [ + "HP:0004397" + ], + "peptic ulcer": [ + "HP:0004398" + ], + "sore in the lining of gastrointestinal tract": [ + "HP:0004398" + ], + "congenital pyloric atresia": [ + "HP:0004399" + ], + "abnormality of the pylorus": [ + "HP:0004400" + ], + "meconium ileus": [ + "HP:0004401" + ], + "distal intestinal obstruction syndrome": [ + "HP:0004401" + ], + "meconium ileus in neonate": [ + "HP:0004401" + ], + "meconium ileus in neonates": [ + "HP:0004401" + ], + "meconium ileus on ultrasonography": [ + "HP:0004401" + ], + "proximal esophageal atresia": [ + "HP:0004403" + ], + "abnormal nipple morphology": [ + "HP:0004404" + ], + "abnormality of the nipple": [ + "HP:0004404" + ], + "prominent nipple": [ + "HP:0004405" + ], + "prominent nipples": [ + "HP:0004405" + ], + "spontaneous , recurrent epistaxis": [ + "HP:0004406" + ], + "recurrent epistaxes": [ + "HP:0004406" + ], + "recurrent epistaxis": [ + "HP:0004406" + ], + "recur nosebleed": [ + "HP:0004406" + ], + "recurring nosebleed": [ + "HP:0004406" + ], + "spontaneous , recurrent nosebleed": [ + "HP:0004406" + ], + "bony paranasal boss": [ + "HP:0004407" + ], + "bony paranasal bossing": [ + "HP:0004407" + ], + "abnormality of the sense of smell": [ + "HP:0004408" + ], + "abnormal sense of smell": [ + "HP:0004408" + ], + "abnormality of olfaction": [ + "HP:0004408" + ], + "smell defect": [ + "HP:0004408" + ], + "hyposmia": [ + "HP:0004409" + ], + "decrease smell sensation": [ + "HP:0004409" + ], + "decreased smell sensation": [ + "HP:0004409" + ], + "sense of smell impair": [ + "HP:0004409" + ], + "sense of smell impaired": [ + "HP:0004409" + ], + "deviate nasal septum": [ + "HP:0004411" + ], + "deviated nasal septum": [ + "HP:0004411" + ], + "crook nasal septum": [ + "HP:0004411" + ], + "crooked nasal septum": [ + "HP:0004411" + ], + "crooked septum of nose": [ + "HP:0004411" + ], + "deviate septum of nose": [ + "HP:0004411" + ], + "deviated septum of nose": [ + "HP:0004411" + ], + "abnormality of the pulmonary artery": [ + "HP:0004414" + ], + "abnormality of lung artery": [ + "HP:0004414" + ], + "pulmonary artery stenosis": [ + "HP:0004415" + ], + "narrowing of lung artery": [ + "HP:0004415" + ], + "precocious atherosclerosis": [ + "HP:0004416" + ], + "premature atherosclerosis": [ + "HP:0004416" + ], + "premature plaque build - up in artery": [ + "HP:0004416" + ], + "premature plaque build - up in arteries": [ + "HP:0004416" + ], + "intermittent claudication": [ + "HP:0004417" + ], + "thrombophlebitis": [ + "HP:0004418" + ], + "recurrent thrombophlebitis": [ + "HP:0004419" + ], + "recurrent phlebitis": [ + "HP:0004419" + ], + "recurrent thrombosis": [ + "HP:0004419" + ], + "arterial thrombosis": [ + "HP:0004420" + ], + "blood clot in artery": [ + "HP:0004420" + ], + "elevate systolic blood pressure": [ + "HP:0004421" + ], + "elevated systolic blood pressure": [ + "HP:0004421" + ], + "elevate systolic bp": [ + "HP:0004421" + ], + "elevated systolic bp": [ + "HP:0004421" + ], + "biparietal narrowing": [ + "HP:0004422" + ], + "decrease width of the skull": [ + "HP:0004422" + ], + "decreased width of the skull": [ + "HP:0004422" + ], + "cranium bifidum occultum": [ + "HP:0004423" + ], + "flat forehead": [ + "HP:0004425" + ], + "flatten forehead": [ + "HP:0004425" + ], + "flattened forehead": [ + "HP:0004425" + ], + "frontal flattening": [ + "HP:0004425" + ], + "abnormality of the cheek": [ + "HP:0004426" + ], + "abnormality of the cheeks": [ + "HP:0004426" + ], + "anomaly of the cheek": [ + "HP:0004426" + ], + "anomaly of the cheeks": [ + "HP:0004426" + ], + "deformity of the cheek": [ + "HP:0004426" + ], + "deformity of the cheeks": [ + "HP:0004426" + ], + "malformation of the cheek": [ + "HP:0004426" + ], + "malformation of the cheeks": [ + "HP:0004426" + ], + "elfin facies": [ + "HP:0004428" + ], + "elf - like facial appearance": [ + "HP:0004428" + ], + "elf - like facial feature": [ + "HP:0004428" + ], + "elf - like facial features": [ + "HP:0004428" + ], + "leprechaun facies": [ + "HP:0004428" + ], + "recurrent viral infection": [ + "HP:0004429" + ], + "recurrent viral infections": [ + "HP:0004429" + ], + "severe combine immunodeficiency": [ + "HP:0004430" + ], + "severe combined immunodeficiency": [ + "HP:0004430" + ], + "immunodeficiency , severe combine": [ + "HP:0004430" + ], + "immunodeficiency , severe combined": [ + "HP:0004430" + ], + "complement deficiency": [ + "HP:0004431" + ], + "agammaglobulinemia": [ + "HP:0004432" + ], + "agammaglobulinaemia": [ + "HP:0004432" + ], + "secretory iga deficiency": [ + "HP:0004433" + ], + "decrease serum complement c8": [ + "HP:0004434" + ], + "decreased serum complement c8": [ + "HP:0004434" + ], + "c8 deficiency": [ + "HP:0004434" + ], + "cranial hyperostosis": [ + "HP:0004437" + ], + "enlargement of skull bone": [ + "HP:0004437" + ], + "enlargement of skull bones": [ + "HP:0004437" + ], + "excessive growth of skull bone": [ + "HP:0004437" + ], + "excessive growth of skull bones": [ + "HP:0004437" + ], + "hyperostosis of cranial bone": [ + "HP:0004437" + ], + "hyperostosis of cranial bones": [ + "HP:0004437" + ], + "hyperostosis of cranial vault": [ + "HP:0004437" + ], + "hypertrophy of cranial bone": [ + "HP:0004437" + ], + "hypertrophy of cranial bones": [ + "HP:0004437" + ], + "increase ossification of cranial bone": [ + "HP:0004437" + ], + "increased ossification of cranial bones": [ + "HP:0004437" + ], + "overgrowth of skull bone": [ + "HP:0004437" + ], + "overgrowth of skull bones": [ + "HP:0004437" + ], + "thick skull bone": [ + "HP:0004437" + ], + "thick skull bones": [ + "HP:0004437" + ], + "hyperostosis frontalis interna": [ + "HP:0004438" + ], + "enlargement of the inner surface of the frontal bone": [ + "HP:0004438" + ], + "excessive growth of inner surface of the frontal bone": [ + "HP:0004438" + ], + "hyperostosis of the internal surface of the frontal bone": [ + "HP:0004438" + ], + "hypertrophy of the internal surface of the frontal bone": [ + "HP:0004438" + ], + "increase ossification of the internal surface of the frontal bone": [ + "HP:0004438" + ], + "increased ossification of the internal surface of the frontal bone": [ + "HP:0004438" + ], + "overgrowth of the inner surface of the frontal bone": [ + "HP:0004438" + ], + "overgrowth of the inside of the frontal bone": [ + "HP:0004438" + ], + "thick inner surface of the frontal bone": [ + "HP:0004438" + ], + "thick internal surface of the frontal bone": [ + "HP:0004438" + ], + "craniofacial dysostosis": [ + "HP:0004439" + ], + "crouzon syndrome": [ + "HP:0004439" + ], + "coronal craniosynostosis": [ + "HP:0004440" + ], + "coronal suture craniosynostosis": [ + "HP:0004440" + ], + "coronal suture synostosis": [ + "HP:0004440" + ], + "craniosynostosis of coronal suture": [ + "HP:0004440" + ], + "sagittal craniosynostosis": [ + "HP:0004442" + ], + "craniosynostosis , sagittal": [ + "HP:0004442" + ], + "craniosynostosis , sagittal suture": [ + "HP:0004442" + ], + "early closure of midline skull joint": [ + "HP:0004442" + ], + "midline skull joint close early": [ + "HP:0004442" + ], + "midline skull joint closes early": [ + "HP:0004442" + ], + "sagittal suture synostosis": [ + "HP:0004442" + ], + "lambdoidal craniosynostosis": [ + "HP:0004443" + ], + "lambdoid suture craniosynostosis": [ + "HP:0004443" + ], + "lambdoid suture synostosis": [ + "HP:0004443" + ], + "spherocytosis": [ + "HP:0004444" + ], + "elliptocytosis": [ + "HP:0004445" + ], + "elliptocyte": [ + "HP:0004445" + ], + "hereditary elliptocytosis": [ + "HP:0004445" + ], + "ovalocytes": [ + "HP:0004445" + ], + "ovalocytosis": [ + "HP:0004445" + ], + "stomatocytosis": [ + "HP:0004446" + ], + "erythrocyte stomatocytes": [ + "HP:0004446" + ], + "red cell stomatocytosis": [ + "HP:0004446" + ], + "poikilocytosis": [ + "HP:0004447" + ], + "fulminant hepatic failure": [ + "HP:0004448" + ], + "preauricular skin furrow": [ + "HP:0004450" + ], + "preauricular skin furrows": [ + "HP:0004450" + ], + "preauricular skin groove": [ + "HP:0004450" + ], + "preauricular skin sulcus": [ + "HP:0004450" + ], + "skin groove in front of the ear": [ + "HP:0004450" + ], + "skin sulcus in front of the ear": [ + "HP:0004450" + ], + "postauricular skin tag": [ + "HP:0004451" + ], + "postauricular acrochordon": [ + "HP:0004451" + ], + "postauricular fibroepithelial polyp": [ + "HP:0004451" + ], + "skin tag behind the ear": [ + "HP:0004451" + ], + "abnormality of the middle ear ossicle": [ + "HP:0004452" + ], + "abnormality of the middle ear ossicles": [ + "HP:0004452" + ], + "malformed ossicle": [ + "HP:0004452" + ], + "malformed ossicles": [ + "HP:0004452" + ], + "ossicular malformation": [ + "HP:0004452" + ], + "overfolding of the superior helix": [ + "HP:0004453" + ], + "overfolding of the superior helices": [ + "HP:0004453" + ], + "overfolding of superior helix": [ + "HP:0004453" + ], + "abnormal middle ear reflex": [ + "HP:0004454" + ], + "abnormal middle ear reflexes": [ + "HP:0004454" + ], + "dilatated internal auditory canal": [ + "HP:0004458" + ], + "bulbous internal auditory canal": [ + "HP:0004458" + ], + "enlarge internal auditory canal": [ + "HP:0004458" + ], + "enlarged internal auditory canal": [ + "HP:0004458" + ], + "exostosis of the external auditory canal": [ + "HP:0004459" + ], + "external auditory canal exostosis": [ + "HP:0004459" + ], + "external auditory canal exostoses": [ + "HP:0004459" + ], + "congenital earlobe sinus": [ + "HP:0004461" + ], + "congenital earlobe sinuses": [ + "HP:0004461" + ], + "absent brainstem auditory response": [ + "HP:0004463" + ], + "absent brainstem auditory responses": [ + "HP:0004463" + ], + "no auditory brainstem response": [ + "HP:0004463" + ], + "postauricular pit": [ + "HP:0004464" + ], + "pit behind the ear": [ + "HP:0004464" + ], + "postauricular earpits": [ + "HP:0004464" + ], + "postauricular fistula": [ + "HP:0004464" + ], + "posterior auricular pit": [ + "HP:0004464" + ], + "posterior auricular sinus": [ + "HP:0004464" + ], + "prolonged brainstem auditory evoke potential": [ + "HP:0004466" + ], + "prolonged brainstem auditory evoked potentials": [ + "HP:0004466" + ], + "preauricular pit": [ + "HP:0004467" + ], + "ear pit": [ + "HP:0004467" + ], + "pit in front of the ear": [ + "HP:0004467" + ], + "preauricular earpits": [ + "HP:0004467" + ], + "preauricular fistula": [ + "HP:0004467" + ], + "preauricular fistulas": [ + "HP:0004467" + ], + "preauricular pits": [ + "HP:0004467" + ], + "preauricular sinus": [ + "HP:0004467" + ], + "anomalous tracheal cartilage": [ + "HP:0004468" + ], + "abnormal tracheal cartilaginous ring": [ + "HP:0004468" + ], + "chronic bronchitis": [ + "HP:0004469" + ], + "atretic occipital cephalocele": [ + "HP:0004470" + ], + "aplasia cutis congenita over the scalp vertex": [ + "HP:0004471" + ], + "absent cutis congenita of vertex": [ + "HP:0004471" + ], + "aplasia cutis congenita of vertex": [ + "HP:0004471" + ], + "mandibular hyperostosis": [ + "HP:0004472" + ], + "excessive growth of mandibular bone": [ + "HP:0004472" + ], + "hyperostosis of low jaw": [ + "HP:0004472" + ], + "hyperostosis of lower jaw": [ + "HP:0004472" + ], + "hyperostosis of mandibular bone": [ + "HP:0004472" + ], + "increase ossification of low jaw": [ + "HP:0004472" + ], + "increased ossification of lower jaw": [ + "HP:0004472" + ], + "increase ossification of mandible": [ + "HP:0004472" + ], + "increased ossification of mandible": [ + "HP:0004472" + ], + "increase ossification of mandibular bone": [ + "HP:0004472" + ], + "increased ossification of mandibular bone": [ + "HP:0004472" + ], + "overgrowth of mandibular bone": [ + "HP:0004472" + ], + "thick low jaw bone": [ + "HP:0004472" + ], + "thick lower jaw bone": [ + "HP:0004472" + ], + "thick mandibular bone": [ + "HP:0004472" + ], + "persistent open anterior fontanelle": [ + "HP:0004474" + ], + "anterior fontanelle open in adult": [ + "HP:0004474" + ], + "anterior fontanelle open in adults": [ + "HP:0004474" + ], + "front fontanelle stay open": [ + "HP:0004474" + ], + "front fontanelle stays open": [ + "HP:0004474" + ], + "persistent , open anterior fontanel": [ + "HP:0004474" + ], + "aplasia cutis congenita over parietal area": [ + "HP:0004476" + ], + "absent cutis congenita over parietal area": [ + "HP:0004476" + ], + "ethmoidal encephalocele": [ + "HP:0004478" + ], + "progressive macrocephaly": [ + "HP:0004481" + ], + "macrocephaly , progressive": [ + "HP:0004481" + ], + "progressively abnormally enlarge cranium": [ + "HP:0004481" + ], + "progressively abnormally enlarging cranium": [ + "HP:0004481" + ], + "progressively abnormally enlarge skull": [ + "HP:0004481" + ], + "progressively abnormally enlarging skull": [ + "HP:0004481" + ], + "relative macrocephaly": [ + "HP:0004482" + ], + "disproportionately large head": [ + "HP:0004482" + ], + "macrocephaly , relative": [ + "HP:0004482" + ], + "relatively large head": [ + "HP:0004482" + ], + "craniofacial asymmetry": [ + "HP:0004484" + ], + "abnormality of craniofacial shape": [ + "HP:0004484" + ], + "malformation of craniofacial shape": [ + "HP:0004484" + ], + "uneven craniofacial structure": [ + "HP:0004484" + ], + "uneven craniofacial structures": [ + "HP:0004484" + ], + "cessation of head growth": [ + "HP:0004485" + ], + "cranium stop grow": [ + "HP:0004485" + ], + "cranium stopped growing": [ + "HP:0004485" + ], + "head stop grow": [ + "HP:0004485" + ], + "head stopped growing": [ + "HP:0004485" + ], + "skull stop grow": [ + "HP:0004485" + ], + "skull stopped growing": [ + "HP:0004485" + ], + "acrobrachycephaly": [ + "HP:0004487" + ], + "macrocephaly at birth": [ + "HP:0004488" + ], + "big cranium present at birth": [ + "HP:0004488" + ], + "big cranium present since birth": [ + "HP:0004488" + ], + "big head present at birth": [ + "HP:0004488" + ], + "big head present since birth": [ + "HP:0004488" + ], + "big skull present at birth": [ + "HP:0004488" + ], + "big skull present since birth": [ + "HP:0004488" + ], + "congenital large cranium": [ + "HP:0004488" + ], + "congenital large head": [ + "HP:0004488" + ], + "congenital large skull": [ + "HP:0004488" + ], + "congenital macrocephaly": [ + "HP:0004488" + ], + "head circumference large for gestational age": [ + "HP:0004488" + ], + "large cranium present at birth": [ + "HP:0004488" + ], + "large cranium present since birth": [ + "HP:0004488" + ], + "large head present at birth": [ + "HP:0004488" + ], + "large head present since birth": [ + "HP:0004488" + ], + "large skull present at birth": [ + "HP:0004488" + ], + "large skull present since birth": [ + "HP:0004488" + ], + "calvarial hyperostosis": [ + "HP:0004490" + ], + "enlargement of calvarial bone": [ + "HP:0004490" + ], + "enlargement of calvarial bones": [ + "HP:0004490" + ], + "excessive growth of calvarial bone": [ + "HP:0004490" + ], + "excessive growth of calvarial bones": [ + "HP:0004490" + ], + "hyperostosis of calvarial bone": [ + "HP:0004490" + ], + "hyperostosis of calvarial bones": [ + "HP:0004490" + ], + "hypertrophy of calvarial bone": [ + "HP:0004490" + ], + "hypertrophy of calvarial bones": [ + "HP:0004490" + ], + "increase ossification of calvarial bone": [ + "HP:0004490" + ], + "increased ossification of calvarial bones": [ + "HP:0004490" + ], + "overgrowth of calvarial bone": [ + "HP:0004490" + ], + "overgrowth of calvarial bones": [ + "HP:0004490" + ], + "overgrowth of skullcap": [ + "HP:0004490" + ], + "thick calvarial bone": [ + "HP:0004490" + ], + "thick calvarial bones": [ + "HP:0004490" + ], + "large posterior fontanelle": [ + "HP:0004491" + ], + "large posterior fontanel": [ + "HP:0004491" + ], + "widely patent fontanelle and suture": [ + "HP:0004492" + ], + "widely patent fontanelles and sutures": [ + "HP:0004492" + ], + "widely patent fontanel and suture": [ + "HP:0004492" + ], + "widely patent fontanels and sutures": [ + "HP:0004492" + ], + "craniofacial hyperostosis": [ + "HP:0004493" + ], + "enlargement of craniofacial bone": [ + "HP:0004493" + ], + "enlargement of craniofacial bones": [ + "HP:0004493" + ], + "excessive bone growth of the skull and face": [ + "HP:0004493" + ], + "excessive growth of craniofacial bone": [ + "HP:0004493" + ], + "excessive growth of craniofacial bones": [ + "HP:0004493" + ], + "hyperostosis of craniofacial bone": [ + "HP:0004493" + ], + "hyperostosis of craniofacial bones": [ + "HP:0004493" + ], + "hypertrophy of craniofacial bone": [ + "HP:0004493" + ], + "hypertrophy of craniofacial bones": [ + "HP:0004493" + ], + "increase ossification of craniofacial bone": [ + "HP:0004493" + ], + "increased ossification of craniofacial bones": [ + "HP:0004493" + ], + "overgrowth of craniofacial bone": [ + "HP:0004493" + ], + "overgrowth of craniofacial bones": [ + "HP:0004493" + ], + "thick craniofacial bone": [ + "HP:0004493" + ], + "thick craniofacial bones": [ + "HP:0004493" + ], + "thin anteverted naris": [ + "HP:0004495" + ], + "thin anteverted nares": [ + "HP:0004495" + ], + "posterior choanal atresia": [ + "HP:0004496" + ], + "chronic rhinitis due to narrow nasal airway": [ + "HP:0004499" + ], + "chronic nasal inflammation due to narrow nasal airway": [ + "HP:0004499" + ], + "bilateral choanal atresia": [ + "HP:0004502" + ], + "bilateral blockage of the rear opening of the nasal cavity": [ + "HP:0004502" + ], + "bilateral obstruction of the rear opening of the nasal cavity": [ + "HP:0004502" + ], + "pancreatic islet - cell hyperplasia": [ + "HP:0004510" + ], + "hyperplastic islet of langerhans": [ + "HP:0004510" + ], + "hyperplastic islets of langerhans": [ + "HP:0004510" + ], + "hypertrophic pancreatic islet": [ + "HP:0004510" + ], + "hypertrophic pancreatic islets": [ + "HP:0004510" + ], + "islet of langerhans hyperplasia": [ + "HP:0004510" + ], + "islet of langerhans hypertrophy": [ + "HP:0004510" + ], + "islets of langerhans hypertrophy": [ + "HP:0004510" + ], + "pancreatic islet - cell hypertrophy": [ + "HP:0004510" + ], + "long eyebrow": [ + "HP:0004523" + ], + "long eyebrows": [ + "HP:0004523" + ], + "elongate eyebrow": [ + "HP:0004523" + ], + "elongated eyebrow": [ + "HP:0004523" + ], + "increase horizontal length of eyebrow": [ + "HP:0004523" + ], + "increased horizontal length of eyebrow": [ + "HP:0004523" + ], + "increased transverse length of eyebrow": [ + "HP:0004523" + ], + "temporal hypotrichosis": [ + "HP:0004524" + ], + "reduce hair growth in temporal region": [ + "HP:0004524" + ], + "reduced hair growth in temporal region": [ + "HP:0004524" + ], + "large clump of pigment irregularly distribute along hair shaft": [ + "HP:0004527" + ], + "large clumps of pigment irregularly distributed along hair shaft": [ + "HP:0004527" + ], + "generalize hypotrichosis": [ + "HP:0004528" + ], + "generalized hypotrichosis": [ + "HP:0004528" + ], + "generalise hypotrichosis": [ + "HP:0004528" + ], + "generalised hypotrichosis": [ + "HP:0004528" + ], + "hypotrichosis , generalise": [ + "HP:0004528" + ], + "hypotrichosis , generalised": [ + "HP:0004528" + ], + "hypotrichosis , generalize": [ + "HP:0004528" + ], + "hypotrichosis , generalized": [ + "HP:0004528" + ], + "atrophic , patchy alopecia": [ + "HP:0004529" + ], + "sacral hypertrichosis": [ + "HP:0004532" + ], + "anterior cervical hypertrichosis": [ + "HP:0004535" + ], + "congenital cervical hypertrichosis": [ + "HP:0004535" + ], + "hypertrichosis , congenital anterior cervical": [ + "HP:0004535" + ], + "congenital , generalize hypertrichosis": [ + "HP:0004540" + ], + "congenital , generalized hypertrichosis": [ + "HP:0004540" + ], + "congenital generalise hypertrichosis": [ + "HP:0004540" + ], + "congenital generalised hypertrichosis": [ + "HP:0004540" + ], + "congenital generalize hypertrichosis": [ + "HP:0004540" + ], + "congenital generalized hypertrichosis": [ + "HP:0004540" + ], + "congenital , generalise hypertrichosis": [ + "HP:0004540" + ], + "congenital , generalised hypertrichosis": [ + "HP:0004540" + ], + "hypertrichosis universalis": [ + "HP:0004540" + ], + "obsolete point frontal hairline": [ + "HP:0004544" + ], + "obsolete pointed frontal hairline": [ + "HP:0004544" + ], + "scar alopecia of scalp": [ + "HP:0004552" + ], + "scarring alopecia of scalp": [ + "HP:0004552" + ], + "cicatricial alopecia": [ + "HP:0004552" + ], + "hair loss on scalp from scar condition": [ + "HP:0004552" + ], + "hair loss on scalp from scarring condition": [ + "HP:0004552" + ], + "generalize hypertrichosis": [ + "HP:0004554" + ], + "generalized hypertrichosis": [ + "HP:0004554" + ], + "generalise hypertrichosis": [ + "HP:0004554" + ], + "generalised hypertrichosis": [ + "HP:0004554" + ], + "anterior vertebral fusion": [ + "HP:0004557" + ], + "cervical platyspondyly": [ + "HP:0004558" + ], + "flatten cervical vertebral body": [ + "HP:0004558" + ], + "flattened cervical vertebral bodies": [ + "HP:0004558" + ], + "beaking of vertebral body t12 - l3": [ + "HP:0004562" + ], + "beaking of vertebral bodies t12 - l3": [ + "HP:0004562" + ], + "increase spinal bone density": [ + "HP:0004563" + ], + "increased spinal bone density": [ + "HP:0004563" + ], + "compact spinal bone": [ + "HP:0004563" + ], + "concrete spinal bone": [ + "HP:0004563" + ], + "dense spinal bone": [ + "HP:0004563" + ], + "eburnation of spinal bone": [ + "HP:0004563" + ], + "increase density of spinal bone": [ + "HP:0004563" + ], + "increased density of spinal bone": [ + "HP:0004563" + ], + "increase spinal bone density z": [ + "HP:0004563" + ], + "increased spinal bone density z": [ + "HP:0004563" + ], + "ivory spinal bone": [ + "HP:0004563" + ], + "sclerosis of spinal bone": [ + "HP:0004563" + ], + "severe platyspondyly": [ + "HP:0004565" + ], + "platyspondyly , extreme": [ + "HP:0004565" + ], + "pear - shape vertebra": [ + "HP:0004566" + ], + "pear - shaped vertebrae": [ + "HP:0004566" + ], + "pear - shaped vertebral body": [ + "HP:0004566" + ], + "pear - shaped vertebral bodies": [ + "HP:0004566" + ], + "beaking of vertebral body": [ + "HP:0004568" + ], + "beaking of vertebral bodies": [ + "HP:0004568" + ], + "anterior beak": [ + "HP:0004568" + ], + "anterior beaking": [ + "HP:0004568" + ], + "anterior beaking of vertebra": [ + "HP:0004568" + ], + "anterior beaking of vertebrae": [ + "HP:0004568" + ], + "anterior beaking of vertebral body": [ + "HP:0004568" + ], + "anterior beaking of vertebral bodies": [ + "HP:0004568" + ], + "beak vertebral body": [ + "HP:0004568" + ], + "beaked vertebral bodies": [ + "HP:0004568" + ], + "vertebral tongue - like protrusion": [ + "HP:0004568" + ], + "increase vertebral height": [ + "HP:0004570" + ], + "increased vertebral height": [ + "HP:0004570" + ], + "tall vertebral body": [ + "HP:0004570" + ], + "tall vertebral bodies": [ + "HP:0004570" + ], + "widening of cervical spinal canal": [ + "HP:0004571" + ], + "anterior wedging of t11": [ + "HP:0004573" + ], + "anterior wedging of the 11th thoracic vertebra": [ + "HP:0004573" + ], + "wedge - shape 11th thoracic vertebra": [ + "HP:0004573" + ], + "wedge - shaped 11th thoracic vertebra": [ + "HP:0004573" + ], + "fusion of midcervical facet joint": [ + "HP:0004575" + ], + "fusion of midcervical facet joints": [ + "HP:0004575" + ], + "sclerotic vertebral endplate": [ + "HP:0004576" + ], + "sclerotic vertebral endplates": [ + "HP:0004576" + ], + "endplate sclerosis": [ + "HP:0004576" + ], + "anterior scalloping of vertebral body": [ + "HP:0004580" + ], + "anterior scalloping of vertebral bodies": [ + "HP:0004580" + ], + "anterior scallop vertebral body": [ + "HP:0004580" + ], + "anterior scalloping vertebral bodies": [ + "HP:0004580" + ], + "increase anterior vertebral height": [ + "HP:0004581" + ], + "increased anterior vertebral height": [ + "HP:0004581" + ], + "irregularity of vertebral body": [ + "HP:0004582" + ], + "irregularity of vertebral bodies": [ + "HP:0004582" + ], + "biconcave vertebral body": [ + "HP:0004586" + ], + "biconcave vertebral bodies": [ + "HP:0004586" + ], + "biconcave 'codfish ' vertebra": [ + "HP:0004586" + ], + "biconcave 'codfish ' vertebrae": [ + "HP:0004586" + ], + "biconcave vertebra": [ + "HP:0004586" + ], + "biconcave vertebrae": [ + "HP:0004586" + ], + "codfish vertebra": [ + "HP:0004586" + ], + "codfish vertebrae": [ + "HP:0004586" + ], + "fish vertebra": [ + "HP:0004586" + ], + "fish vertebrae": [ + "HP:0004586" + ], + "scalloping of vertebral body": [ + "HP:0004586" + ], + "scalloping of vertebral bodies": [ + "HP:0004586" + ], + "dysplasia of second lumbar vertebra": [ + "HP:0004589" + ], + "hypoplastic sacrum": [ + "HP:0004590" + ], + "small sacrum": [ + "HP:0004590" + ], + "disc - like vertebral body": [ + "HP:0004591" + ], + "disc - like vertebral bodies": [ + "HP:0004591" + ], + "thoracic platyspondyly": [ + "HP:0004592" + ], + "hump - shape mound of bone in central and posterior portion of vertebral endplate": [ + "HP:0004594" + ], + "hump - shaped mound of bone in central and posterior portions of vertebral endplate": [ + "HP:0004594" + ], + "supernumerary vertebral ossification center": [ + "HP:0004598" + ], + "supernumerary vertebral ossification centers": [ + "HP:0004598" + ], + "supernumerary vertebral ossification centre": [ + "HP:0004598" + ], + "supernumerary vertebral ossification centres": [ + "HP:0004598" + ], + "absent or minimally ossified vertebral body": [ + "HP:0004599" + ], + "absent or minimally ossified vertebral bodies": [ + "HP:0004599" + ], + "spina bifida occulta at l5": [ + "HP:0004601" + ], + "cervical c2 / c3 vertebral fusion": [ + "HP:0004602" + ], + "fusion of cervical vertebra c2 - 3": [ + "HP:0004602" + ], + "fusion of cervical vertebrae c2 - 3": [ + "HP:0004602" + ], + "klippel - feil anomaly": [ + "HP:0004602" + ], + "klippel - feil syndrome": [ + "HP:0004602" + ], + "hyperconvex vertebral body endplate": [ + "HP:0004603" + ], + "hyperconvex vertebral body endplates": [ + "HP:0004603" + ], + "absent vertebral body mineralization": [ + "HP:0004605" + ], + "unossified vertebral body": [ + "HP:0004606" + ], + "unossified vertebral bodies": [ + "HP:0004606" + ], + "anterior beaking of low thoracic vertebra": [ + "HP:0004607" + ], + "anterior beaking of lower thoracic vertebrae": [ + "HP:0004607" + ], + "anteriorly place odontoid process": [ + "HP:0004608" + ], + "anteriorly placed odontoid process": [ + "HP:0004608" + ], + "patchy distortion of vertebra": [ + "HP:0004609" + ], + "patchy distortion of vertebrae": [ + "HP:0004609" + ], + "lumbar spinal canal stenosis": [ + "HP:0004610" + ], + "lumbar spinal stenosis": [ + "HP:0004610" + ], + "narrow lumbar spinal canal": [ + "HP:0004610" + ], + "anterior concavity of thoracic vertebra": [ + "HP:0004611" + ], + "anterior concavity of thoracic vertebrae": [ + "HP:0004611" + ], + "anteriorly concave vertebra": [ + "HP:0004611" + ], + "anteriorly concave vertebrae": [ + "HP:0004611" + ], + "spina bifida occulta at s1": [ + "HP:0004614" + ], + "cleft vertebral arch": [ + "HP:0004616" + ], + "cleft vertebral arches": [ + "HP:0004616" + ], + "butterfly vertebral arch": [ + "HP:0004617" + ], + "sandwich appearance of vertebral body": [ + "HP:0004618" + ], + "sandwich appearance of vertebral bodies": [ + "HP:0004618" + ], + "lumbar kyphoscoliosis": [ + "HP:0004619" + ], + "enlarged vertebral pedicle": [ + "HP:0004621" + ], + "enlarged vertebral pedicles": [ + "HP:0004621" + ], + "hyperplastic vertebral pedicle": [ + "HP:0004621" + ], + "hyperplastic vertebral pedicles": [ + "HP:0004621" + ], + "progressive intervertebral space narrowing": [ + "HP:0004622" + ], + "biconvex vertebral body": [ + "HP:0004625" + ], + "biconvex vertebral bodies": [ + "HP:0004625" + ], + "lumbar scoliosis": [ + "HP:0004626" + ], + "small cervical vertebral body": [ + "HP:0004629" + ], + "small cervical vertebral bodies": [ + "HP:0004629" + ], + "small cervical vertebra": [ + "HP:0004629" + ], + "small cervical vertebrae": [ + "HP:0004629" + ], + "anterior beaking of thoracic vertebra": [ + "HP:0004630" + ], + "anterior beaking of thoracic vertebrae": [ + "HP:0004630" + ], + "decreased cervical spine flexion due to contracture of posterior cervical muscle": [ + "HP:0004631" + ], + "decreased cervical spine flexion due to contractures of posterior cervical muscles": [ + "HP:0004631" + ], + "contracture of post - cervical muscle": [ + "HP:0004631" + ], + "contracture of post - cervical muscles": [ + "HP:0004631" + ], + "inability to touch chin to chest": [ + "HP:0004631" + ], + "cervical segmentation defect": [ + "HP:0004632" + ], + "cervical spine segmentation defect": [ + "HP:0004632" + ], + "low thoracic kyphosis": [ + "HP:0004633" + ], + "lower thoracic kyphosis": [ + "HP:0004633" + ], + "round mid - back": [ + "HP:0004633" + ], + "cuboid - shaped vertebral body": [ + "HP:0004634" + ], + "cuboid - shaped vertebral bodies": [ + "HP:0004634" + ], + "cuboid vertebral body": [ + "HP:0004634" + ], + "cuboid vertebral bodies": [ + "HP:0004634" + ], + "cervical c5 / c6 vertebra fusion": [ + "HP:0004635" + ], + "cervical c5 / c6 vertebrae fusion": [ + "HP:0004635" + ], + "decreased cervical spine mobility": [ + "HP:0004637" + ], + "limited neck movement": [ + "HP:0004637" + ], + "elevate amniotic fluid alpha - fetoprotein": [ + "HP:0004639" + ], + "elevated amniotic fluid alpha - fetoprotein": [ + "HP:0004639" + ], + "elevate amniotic fluid alpha fetal protein": [ + "HP:0004639" + ], + "elevated amniotic fluid alpha fetal protein": [ + "HP:0004639" + ], + "elevate amniotic fluid alpha foetal protein": [ + "HP:0004639" + ], + "elevated amniotic fluid alpha foetal protein": [ + "HP:0004639" + ], + "elevate amniotic fluid alpha - 1 - fetoprotein": [ + "HP:0004639" + ], + "elevated amniotic fluid alpha - 1 - fetoprotein": [ + "HP:0004639" + ], + "elevate amniotic fluid alpha - fetoglobulin": [ + "HP:0004639" + ], + "elevated amniotic fluid alpha - fetoglobulin": [ + "HP:0004639" + ], + "hypoplasia of the nasal bone": [ + "HP:0004646" + ], + "decreased size of nasal bone": [ + "HP:0004646" + ], + "deficiency of nasal bone": [ + "HP:0004646" + ], + "hypotrophic nasal bone": [ + "HP:0004646" + ], + "nasal bone hypoplasia": [ + "HP:0004646" + ], + "small nasal bone": [ + "HP:0004646" + ], + "underdevelopment of nasal bone": [ + "HP:0004646" + ], + "hypoplasia of facial musculature": [ + "HP:0004660" + ], + "atrophy of facial musculature": [ + "HP:0004660" + ], + "decreased size of facial muscle": [ + "HP:0004660" + ], + "decreased size of facial muscles": [ + "HP:0004660" + ], + "deficiency of facial musculature": [ + "HP:0004660" + ], + "hypotrophic facial musculature": [ + "HP:0004660" + ], + "small facial muscle": [ + "HP:0004660" + ], + "small facial muscles": [ + "HP:0004660" + ], + "underdevelopment of facial muscle": [ + "HP:0004660" + ], + "underdevelopment of facial muscles": [ + "HP:0004660" + ], + "frontalis muscle weakness": [ + "HP:0004661" + ], + "weak frontalis muscle": [ + "HP:0004661" + ], + "weakness of forehead muscle": [ + "HP:0004661" + ], + "facial midline hemangioma": [ + "HP:0004664" + ], + "decreased facial expression": [ + "HP:0004673" + ], + "prominent supraorbital arch in adult": [ + "HP:0004676" + ], + "prominent supraorbital arches in adult": [ + "HP:0004676" + ], + "large tarsal bone": [ + "HP:0004679" + ], + "large tarsal bones": [ + "HP:0004679" + ], + "large ankle bone": [ + "HP:0004679" + ], + "large ankle bones": [ + "HP:0004679" + ], + "deep longitudinal plantar crease": [ + "HP:0004681" + ], + "foot crease": [ + "HP:0004681" + ], + "longitudinal groove on sol": [ + "HP:0004681" + ], + "longitudinal groove on soles": [ + "HP:0004681" + ], + "talipes valgus": [ + "HP:0004684" + ], + "short third metatarsal": [ + "HP:0004686" + ], + "hypoplasia of the 3rd metatarsal bone": [ + "HP:0004686" + ], + "short 3rd long bone of foot": [ + "HP:0004686" + ], + "irregular tarsal bone": [ + "HP:0004688" + ], + "irregular tarsal bones": [ + "HP:0004688" + ], + "abnormal shape of ankle bone": [ + "HP:0004688" + ], + "abnormal shape of ankle bones": [ + "HP:0004688" + ], + "short fourth metatarsal": [ + "HP:0004689" + ], + "bilateral fourth metatarsal shorten": [ + "HP:0004689" + ], + "bilateral fourth metatarsal shortening": [ + "HP:0004689" + ], + "short 4th long bone of foot": [ + "HP:0004689" + ], + "short fourth metatarsals": [ + "HP:0004689" + ], + "short fourth metatarsus": [ + "HP:0004689" + ], + "thicken achilles tendon": [ + "HP:0004690" + ], + "thickened achilles tendon": [ + "HP:0004690" + ], + "2 - 3 toe syndactyly": [ + "HP:0004691" + ], + "2 - 3 syndactyly of foot": [ + "HP:0004691" + ], + "2 - 3 syndactyly of feet": [ + "HP:0004691" + ], + "2 - 3 toe soft tissue syndactyly": [ + "HP:0004691" + ], + "2 - 3 toes syndactyly": [ + "HP:0004691" + ], + "partial or complete syndactyly 2nd - 3rd toe": [ + "HP:0004691" + ], + "partial or complete syndactyly 2nd - 3rd toes": [ + "HP:0004691" + ], + "syndactyly of second and third toe": [ + "HP:0004691" + ], + "syndactyly of second and third toes": [ + "HP:0004691" + ], + "toe syndactyly , 2 - 3": [ + "HP:0004691" + ], + "web 2nd and 3rd toe": [ + "HP:0004691" + ], + "webbed 2nd and 3rd toes": [ + "HP:0004691" + ], + "4 - 5 toe syndactyly": [ + "HP:0004692" + ], + "symmetric syndactyly , toe 4 and 5": [ + "HP:0004692" + ], + "symmetric syndactyly , toes 4 and 5": [ + "HP:0004692" + ], + "syndactyly of toe 4 and 5": [ + "HP:0004692" + ], + "syndactyly of toes 4 and 5": [ + "HP:0004692" + ], + "web 4th - 5th toe": [ + "HP:0004692" + ], + "webbed 4th - 5th toes": [ + "HP:0004692" + ], + "calcaneal epiphyseal stipple": [ + "HP:0004695" + ], + "calcaneal epiphyseal stippling": [ + "HP:0004695" + ], + "talipes cavus equinovarus": [ + "HP:0004696" + ], + "osteoporotic metatarsal": [ + "HP:0004699" + ], + "short fifth metatarsal": [ + "HP:0004704" + ], + "hypoplasia of the fifth metatarsal bone": [ + "HP:0004704" + ], + "short 5th long bone of foot": [ + "HP:0004704" + ], + "renal malrotation": [ + "HP:0004712" + ], + "abnormal rotation of the kidney": [ + "HP:0004712" + ], + "abnormal rotation of the kidneys": [ + "HP:0004712" + ], + "malrotation of the kidney": [ + "HP:0004712" + ], + "reversible renal failure": [ + "HP:0004713" + ], + "reversible kidney failure": [ + "HP:0004713" + ], + "axial malrotation of the kidney": [ + "HP:0004717" + ], + "hyperechogenic kidney": [ + "HP:0004719" + ], + "hyperechogenic kidneys": [ + "HP:0004719" + ], + "echogenic kidney": [ + "HP:0004719" + ], + "echogenic kidneys": [ + "HP:0004719" + ], + "increase echogenicity of the renal parenchyma": [ + "HP:0004719" + ], + "increased echogenicity of the renal parenchyma": [ + "HP:0004719" + ], + "thicken glomerular basement membrane": [ + "HP:0004722" + ], + "thickened glomerular basement membrane": [ + "HP:0004722" + ], + "calcium nephrolithiasis": [ + "HP:0004724" + ], + "ca kidney stone": [ + "HP:0004724" + ], + "ca nephrolithiasis": [ + "HP:0004724" + ], + "ca2+ kidney stone": [ + "HP:0004724" + ], + "ca2+ nephrolithiasis": [ + "HP:0004724" + ], + "calcium kidney stone": [ + "HP:0004724" + ], + "impaired renal concentrating ability": [ + "HP:0004727" + ], + "urine concentrating defect": [ + "HP:0004727" + ], + "urine concentration defect": [ + "HP:0004727" + ], + "acute tubulointerstitial nephritis": [ + "HP:0004729" + ], + "impaired renal uric acid clearance": [ + "HP:0004732" + ], + "renal cortical microcysts": [ + "HP:0004734" + ], + "cortical microcysts": [ + "HP:0004734" + ], + "multiple renal cortical microcysts": [ + "HP:0004734" + ], + "multiple small renal cortical cyst": [ + "HP:0004734" + ], + "multiple small renal cortical cysts": [ + "HP:0004734" + ], + "cross fused renal ectopia": [ + "HP:0004736" + ], + "crossed fused renal ectopia": [ + "HP:0004736" + ], + "ectopic kidney with fusion": [ + "HP:0004736" + ], + "global glomerulosclerosis": [ + "HP:0004737" + ], + "abnormal renal collecting system morphology": [ + "HP:0004742" + ], + "abnormal collecting system": [ + "HP:0004742" + ], + "abnormality of the renal collecting system": [ + "HP:0004742" + ], + "renal collecting system anomaly": [ + "HP:0004742" + ], + "renal collecting system anomalies": [ + "HP:0004742" + ], + "chronic tubulointerstitial nephritis": [ + "HP:0004743" + ], + "glomerular subendothelial electron - dense deposit": [ + "HP:0004746" + ], + "glomerular subendothelial electron - dense deposits": [ + "HP:0004746" + ], + "dense deposit disease": [ + "HP:0004746" + ], + "membranoproliferative glomerulonephritis type ii": [ + "HP:0004746" + ], + "atrial flutter": [ + "HP:0004749" + ], + "paroxysmal ventricular tachycardia": [ + "HP:0004751" + ], + "episode of ventricular tachycardia": [ + "HP:0004751" + ], + "episodes of ventricular tachycardia": [ + "HP:0004751" + ], + "congenital atrioventricular dissociation": [ + "HP:0004752" + ], + "permanent atrial fibrillation": [ + "HP:0004754" + ], + "chronic atrial fibrillation": [ + "HP:0004754" + ], + "supraventricular tachycardia": [ + "HP:0004755" + ], + "supraventricular tachyarrhythmia": [ + "HP:0004755" + ], + "ventricular tachycardia": [ + "HP:0004756" + ], + "paroxysmal atrial fibrillation": [ + "HP:0004757" + ], + "atrial fibrillation , paroxysmal": [ + "HP:0004757" + ], + "intermittent atrial fibrillation": [ + "HP:0004757" + ], + "paroxysmal af": [ + "HP:0004757" + ], + "effort - induced polymorphic ventricular tachycardia": [ + "HP:0004758" + ], + "catecholaminergic polymorphic ventricular tachycardia": [ + "HP:0004758" + ], + "exercise - induced polymorphic ventricular tachycardia": [ + "HP:0004758" + ], + "obsolete nodular calcific aortic valve disease": [ + "HP:0004759" + ], + "obsolete congenital septal defect": [ + "HP:0004760" + ], + "post - angioplasty coronary artery restenosis": [ + "HP:0004761" + ], + "hypoplasia of right ventricle": [ + "HP:0004762" + ], + "heart right ventricle hypoplasia": [ + "HP:0004762" + ], + "small right heart chamber": [ + "HP:0004762" + ], + "underdeveloped right heart chamber": [ + "HP:0004762" + ], + "paroxysmal supraventricular tachycardia": [ + "HP:0004763" + ], + "episodic rapid heart beat": [ + "HP:0004763" + ], + "episodic supraventricular tachycardia": [ + "HP:0004763" + ], + "myxomatous mitral valve degeneration": [ + "HP:0004764" + ], + "sparse anterior scalp hair": [ + "HP:0004768" + ], + "sparse scalp hair at front of head": [ + "HP:0004768" + ], + "thin scalp hair at front of head": [ + "HP:0004768" + ], + "premature graying of body hair": [ + "HP:0004771" + ], + "premature greying of body hair": [ + "HP:0004771" + ], + "brittle scalp hair": [ + "HP:0004779" + ], + "elbow hypertrichosis": [ + "HP:0004780" + ], + "hairy elbow": [ + "HP:0004780" + ], + "hairy elbow syndrome": [ + "HP:0004780" + ], + "hypertrichosis cubiti": [ + "HP:0004780" + ], + "pilosity of elbow": [ + "HP:0004780" + ], + "obsolete hypotrichosis of the scalp": [ + "HP:0004782" + ], + "duodenal polyposis": [ + "HP:0004783" + ], + "multiple duodenal polyp": [ + "HP:0004783" + ], + "multiple duodenal polyps": [ + "HP:0004783" + ], + "juvenile gastrointestinal polyposis": [ + "HP:0004784" + ], + "juvenile gi polyposis": [ + "HP:0004784" + ], + "malrotation of colon": [ + "HP:0004785" + ], + "jejunal diverticulum": [ + "HP:0004786" + ], + "jejunal diverticula": [ + "HP:0004786" + ], + "fulminant hepatitis": [ + "HP:0004787" + ], + "intestinal lymphedema": [ + "HP:0004788" + ], + "lactose intolerance": [ + "HP:0004789" + ], + "milk intolerance": [ + "HP:0004789" + ], + "hypoplasia of the small intestine": [ + "HP:0004790" + ], + "underdeveloped small intestine": [ + "HP:0004790" + ], + "esophageal ulceration": [ + "HP:0004791" + ], + "esophagus ulcer": [ + "HP:0004791" + ], + "oesophagus ulcer": [ + "HP:0004791" + ], + "oesophagus ulceration": [ + "HP:0004791" + ], + "rectoperineal fistula": [ + "HP:0004792" + ], + "malrotation of small bowel": [ + "HP:0004794" + ], + "malrotation of the small intestine": [ + "HP:0004794" + ], + "hamartomatous stomach polyp": [ + "HP:0004795" + ], + "hamartomatous stomach polyps": [ + "HP:0004795" + ], + "gastrointestinal obstruction": [ + "HP:0004796" + ], + "gi obstruction": [ + "HP:0004796" + ], + "obstruction in digestive tract": [ + "HP:0004796" + ], + "multiple small bowel atresia": [ + "HP:0004797" + ], + "multiple small bowel atresias": [ + "HP:0004797" + ], + "recurrent infection of the gastrointestinal tract": [ + "HP:0004798" + ], + "gastrointestinal infection": [ + "HP:0004798" + ], + "gastrointestinal infections": [ + "HP:0004798" + ], + "gastrointestinal infection , recurrent": [ + "HP:0004798" + ], + "gastrointestinal infections , recurrent": [ + "HP:0004798" + ], + "recurrent gastrointestinal infection": [ + "HP:0004798" + ], + "recurrent gastrointestinal infections": [ + "HP:0004798" + ], + "recurrent infection of the gi tract": [ + "HP:0004798" + ], + "jejunoileal diverticulum": [ + "HP:0004799" + ], + "jejunoileal diverticula": [ + "HP:0004799" + ], + "duodenal diverticulum": [ + "HP:0004800" + ], + "duodenal diverticula": [ + "HP:0004800" + ], + "episodic hemolytic anemia": [ + "HP:0004802" + ], + "episodic hemolysis": [ + "HP:0004802" + ], + "episodic hemolytic anaemia": [ + "HP:0004802" + ], + "congenital hemolytic anemia": [ + "HP:0004804" + ], + "congenital haemolytic anaemia": [ + "HP:0004804" + ], + "congenital haemolytic anemia": [ + "HP:0004804" + ], + "congenital hemolytic anaemia": [ + "HP:0004804" + ], + "neonatal hemolytic anaemia": [ + "HP:0004804" + ], + "neonatal hemolytic anemia": [ + "HP:0004804" + ], + "acute myeloid leukemia": [ + "HP:0004808" + ], + "acute myeloblastic leukaemia": [ + "HP:0004808" + ], + "acute myeloblastic leukemia": [ + "HP:0004808" + ], + "acute myelocytic leukaemia": [ + "HP:0004808" + ], + "acute myelocytic leukemia": [ + "HP:0004808" + ], + "acute myelogenous leukaemia": [ + "HP:0004808" + ], + "acute myelogenous leukemia": [ + "HP:0004808" + ], + "acute myeloid leukaemia": [ + "HP:0004808" + ], + "neonatal alloimmune thrombocytopenia": [ + "HP:0004809" + ], + "congenital hypoplastic anemia": [ + "HP:0004810" + ], + "congenital dyserythropoietic anaemia": [ + "HP:0004810" + ], + "congenital dyserythropoietic anemia": [ + "HP:0004810" + ], + "congenital hypoplastic anaemia": [ + "HP:0004810" + ], + "b acute lymphoblastic leukemia": [ + "HP:0004812" + ], + "b acute lymphoblastic leukaemia": [ + "HP:0004812" + ], + "pre - b - cell acute lymphoblastic leukaemia": [ + "HP:0004812" + ], + "pre - b - cell acute lymphoblastic leukemia": [ + "HP:0004812" + ], + "post - transfusion thrombocytopenia": [ + "HP:0004813" + ], + "post - transfusion purpura": [ + "HP:0004813" + ], + "fava bean - induce hemolytic anemia": [ + "HP:0004814" + ], + "fava bean - induced hemolytic anemia": [ + "HP:0004814" + ], + "fava bean - induce hemolytic anaemia": [ + "HP:0004814" + ], + "fava bean - induced hemolytic anaemia": [ + "HP:0004814" + ], + "hemolytic anaemia follow ingestion of fava bean": [ + "HP:0004814" + ], + "hemolytic anaemia following ingestion of fava beans": [ + "HP:0004814" + ], + "hemolytic anemia follow ingestion of fava bean": [ + "HP:0004814" + ], + "hemolytic anemia following ingestion of fava beans": [ + "HP:0004814" + ], + "drug - sensitive hemolytic anemia": [ + "HP:0004817" + ], + "drug - sensitive hemolytic anaemia": [ + "HP:0004817" + ], + "paroxysmal nocturnal hemoglobinuria": [ + "HP:0004818" + ], + "paroxysmal nocturnal haemoglobinuria": [ + "HP:0004818" + ], + "normocytic hypoplastic anemia": [ + "HP:0004819" + ], + "normocytic hypoplastic anaemia": [ + "HP:0004819" + ], + "acute myelomonocytic leukemia": [ + "HP:0004820" + ], + "acute myelomonocytic leukaemia": [ + "HP:0004820" + ], + "hypersegmentation of neutrophil nucleus": [ + "HP:0004821" + ], + "hypersegmentation of neutrophil nuclei": [ + "HP:0004821" + ], + "hypermature neutrophil": [ + "HP:0004821" + ], + "hypermature neutrophils": [ + "HP:0004821" + ], + "hypersegmentation of neutrophil nucleus in peripheral blood": [ + "HP:0004821" + ], + "hypersegmentation of neutrophil nuclei in peripheral blood": [ + "HP:0004821" + ], + "atypical elliptocytosis": [ + "HP:0004822" + ], + "anisopoikilocytosis": [ + "HP:0004823" + ], + "increase hemoglobin oxygen affinity": [ + "HP:0004825" + ], + "increased hemoglobin oxygen affinity": [ + "HP:0004825" + ], + "increase haemoglobin o2 affinity": [ + "HP:0004825" + ], + "increased haemoglobin o2 affinity": [ + "HP:0004825" + ], + "increase haemoglobin oxygen affinity": [ + "HP:0004825" + ], + "increased haemoglobin oxygen affinity": [ + "HP:0004825" + ], + "increase hb o2 affinity": [ + "HP:0004825" + ], + "increased hb o2 affinity": [ + "HP:0004825" + ], + "increase hb oxygen affinity": [ + "HP:0004825" + ], + "increased hb oxygen affinity": [ + "HP:0004825" + ], + "increase hemoglobin o2 affinity": [ + "HP:0004825" + ], + "increased hemoglobin o2 affinity": [ + "HP:0004825" + ], + "folate - unresponsive megaloblastic anemia": [ + "HP:0004826" + ], + "folate - unresponsive megaloblastic anaemia": [ + "HP:0004826" + ], + "refractory anemia with ringed sideroblast": [ + "HP:0004828" + ], + "refractory anemia with ringed sideroblasts": [ + "HP:0004828" + ], + "myelodysplasia with sideroblastosis": [ + "HP:0004828" + ], + "refractory anaemia with ringed sideroblast": [ + "HP:0004828" + ], + "refractory anaemia with ringed sideroblasts": [ + "HP:0004828" + ], + "recurrent thromboembolism": [ + "HP:0004831" + ], + "recurrent thromboembolic disease": [ + "HP:0004831" + ], + "microspherocytosis": [ + "HP:0004835" + ], + "acute promyelocytic leukemia": [ + "HP:0004836" + ], + "acute promyelocytic leukaemia": [ + "HP:0004836" + ], + "pyropoikilocytosis": [ + "HP:0004839" + ], + "hereditary pyropoikilocytosis": [ + "HP:0004839" + ], + "hypochromic microcytic anemia": [ + "HP:0004840" + ], + "hypochromic microcytic anaemia": [ + "HP:0004840" + ], + "hypochromic , microcytic anaemia": [ + "HP:0004840" + ], + "hypochromic , microcytic anemia": [ + "HP:0004840" + ], + "reduce factor xii activity": [ + "HP:0004841" + ], + "reduced factor xii activity": [ + "HP:0004841" + ], + "factor xii deficiency": [ + "HP:0004841" + ], + "hageman factor deficiency": [ + "HP:0004841" + ], + "coombs - positive hemolytic anemia": [ + "HP:0004844" + ], + "coombs - positive hemolytic anaemia": [ + "HP:0004844" + ], + "direct coombs positive": [ + "HP:0004844" + ], + "acute monocytic leukemia": [ + "HP:0004845" + ], + "acute monoblastic leukaemia": [ + "HP:0004845" + ], + "acute monoblastic leukemia": [ + "HP:0004845" + ], + "acute monocytic leukaemia": [ + "HP:0004845" + ], + "amol": [ + "HP:0004845" + ], + "prolong bleeding after surgery": [ + "HP:0004846" + ], + "prolonged bleeding after surgery": [ + "HP:0004846" + ], + "excessive bleeding during surgery": [ + "HP:0004846" + ], + "protract bleeding after surgery": [ + "HP:0004846" + ], + "protracted bleeding after surgery": [ + "HP:0004846" + ], + "ph - positive acute lymphoblastic leukemia": [ + "HP:0004848" + ], + "ph - positive acute lymphoblastic leukaemia": [ + "HP:0004848" + ], + "philadelphia - positive acute lymphoblastic leukaemia": [ + "HP:0004848" + ], + "philadelphia - positive acute lymphoblastic leukemia": [ + "HP:0004848" + ], + "recurrent deep vein thrombosis": [ + "HP:0004850" + ], + "recurrent deep vein blood clot": [ + "HP:0004850" + ], + "recurrent venous thrombosis": [ + "HP:0004850" + ], + "folate - responsive megaloblastic anemia": [ + "HP:0004851" + ], + "folate - responsive megaloblastic anaemia": [ + "HP:0004851" + ], + "reduce leukocyte alkaline phosphatase": [ + "HP:0004852" + ], + "reduced leukocyte alkaline phosphatase": [ + "HP:0004852" + ], + "low leukocyte alkaline phosphatase": [ + "HP:0004852" + ], + "reduce leukocyte alp": [ + "HP:0004852" + ], + "reduced leukocyte alp": [ + "HP:0004852" + ], + "intermittent thrombocytopenia": [ + "HP:0004854" + ], + "reduce protein s activity": [ + "HP:0004855" + ], + "reduced protein s activity": [ + "HP:0004855" + ], + "protein s deficiency": [ + "HP:0004855" + ], + "normochromic microcytic anemia": [ + "HP:0004856" + ], + "normochromic microcytic anaemia": [ + "HP:0004856" + ], + "hyperchromic macrocytic anemia": [ + "HP:0004857" + ], + "hyperchromic macrocytic anaemia": [ + "HP:0004857" + ], + "amegakaryocytic thrombocytopenia": [ + "HP:0004859" + ], + "thiamine - responsive megaloblastic anemia": [ + "HP:0004860" + ], + "thiamine - responsive megaloblastic anaemia": [ + "HP:0004860" + ], + "refractory macrocytic anemia": [ + "HP:0004861" + ], + "refractory macrocytic anaemia": [ + "HP:0004861" + ], + "compensate hemolytic anemia": [ + "HP:0004863" + ], + "compensated hemolytic anemia": [ + "HP:0004863" + ], + "compensate hemolytic anaemia": [ + "HP:0004863" + ], + "compensated hemolytic anaemia": [ + "HP:0004863" + ], + "refractory sideroblastic anemia": [ + "HP:0004864" + ], + "refractory sideroblastic anaemia": [ + "HP:0004864" + ], + "impaired adp - induced platelet aggregation": [ + "HP:0004866" + ], + "chronic hemolytic anemia": [ + "HP:0004870" + ], + "chronic hemolytic anaemia": [ + "HP:0004870" + ], + "hemolytic anemia , chronic": [ + "HP:0004870" + ], + "perineal fistula": [ + "HP:0004871" + ], + "incisional hernia": [ + "HP:0004872" + ], + "recurrent abdominal hernia": [ + "HP:0004872" + ], + "neonatal inspiratory stridor": [ + "HP:0004875" + ], + "spontaneous neonatal pneumothorax": [ + "HP:0004876" + ], + "neonatal pneumothorax": [ + "HP:0004876" + ], + "intercostal muscle weakness": [ + "HP:0004878" + ], + "dependence on diaphragmatic breathing": [ + "HP:0004878" + ], + "muscle weakness between rib": [ + "HP:0004878" + ], + "muscle weakness between ribs": [ + "HP:0004878" + ], + "intermittent hyperventilation": [ + "HP:0004879" + ], + "episodic hyperventilation": [ + "HP:0004879" + ], + "intermittent overbreathing": [ + "HP:0004879" + ], + "respiratory infection in early life": [ + "HP:0004880" + ], + "respiratory infections in early life": [ + "HP:0004880" + ], + "episodic hypoventilation": [ + "HP:0004881" + ], + "episodic slow breathing": [ + "HP:0004881" + ], + "episodic under breathe": [ + "HP:0004881" + ], + "episodic under breathing": [ + "HP:0004881" + ], + "episodic respiratory distress": [ + "HP:0004885" + ], + "episodic difficulty breathe": [ + "HP:0004885" + ], + "episodic difficulty breathing": [ + "HP:0004885" + ], + "respiratory distress , episodic": [ + "HP:0004885" + ], + "congenital laryngeal stridor": [ + "HP:0004886" + ], + "respiratory failure require assist ventilation": [ + "HP:0004887" + ], + "respiratory failure requiring assisted ventilation": [ + "HP:0004887" + ], + "respiratory distress necessitate mechanical ventilation": [ + "HP:0004887" + ], + "respiratory distress necessitating mechanical ventilation": [ + "HP:0004887" + ], + "respiratory distress require endotracheal intubation": [ + "HP:0004887" + ], + "respiratory distress requiring endotracheal intubation": [ + "HP:0004887" + ], + "respiratory distress require mechanical ventilation": [ + "HP:0004887" + ], + "respiratory distress requiring mechanical ventilation": [ + "HP:0004887" + ], + "intermittent episode of respiratory insufficiency due to muscle weakness": [ + "HP:0004889" + ], + "intermittent episodes of respiratory insufficiency due to muscle weakness": [ + "HP:0004889" + ], + "elevate pulmonary artery pressure": [ + "HP:0004890" + ], + "elevated pulmonary artery pressure": [ + "HP:0004890" + ], + "elevate lung artery pressure": [ + "HP:0004890" + ], + "elevated lung artery pressure": [ + "HP:0004890" + ], + "increase pulmonary artery pressure": [ + "HP:0004890" + ], + "increased pulmonary artery pressure": [ + "HP:0004890" + ], + "recurrent infection due to aspiration": [ + "HP:0004891" + ], + "recurrent infections due to aspiration": [ + "HP:0004891" + ], + "laryngotracheal stenosis": [ + "HP:0004894" + ], + "stress / infection - induced lactic acidosis": [ + "HP:0004897" + ], + "metabolic crisis during febrile infection": [ + "HP:0004897" + ], + "metabolic crises during febrile infections": [ + "HP:0004897" + ], + "persistent lactic acidosis": [ + "HP:0004898" + ], + "severe lactic acidosis": [ + "HP:0004900" + ], + "exercise - induced lactic acidemia": [ + "HP:0004901" + ], + "exercise - induced lactic acidosis": [ + "HP:0004901" + ], + "congenital lactic acidosis": [ + "HP:0004902" + ], + "maturity - onset diabetes of the young": [ + "HP:0004904" + ], + "maturity onset diabetes of the young": [ + "HP:0004904" + ], + "low level of vitamin a": [ + "HP:0004905" + ], + "low levels of vitamin a": [ + "HP:0004905" + ], + "vitamin a deficiency": [ + "HP:0004905" + ], + "hypernatremic dehydration": [ + "HP:0004906" + ], + "hypokalemic hypochloremic metabolic alkalosis": [ + "HP:0004909" + ], + "bicarbonate - waste renal tubular acidosis": [ + "HP:0004910" + ], + "bicarbonate - wasting renal tubular acidosis": [ + "HP:0004910" + ], + "hco3 - waste renal tubular acidosis": [ + "HP:0004910" + ], + "hco3 - wasting renal tubular acidosis": [ + "HP:0004910" + ], + "renal bicarbonate wasting": [ + "HP:0004910" + ], + "episodic metabolic acidosis": [ + "HP:0004911" + ], + "recurrent episode of acidosis": [ + "HP:0004911" + ], + "recurrent episodes of acidosis": [ + "HP:0004911" + ], + "hypophosphatemic rickets": [ + "HP:0004912" + ], + "intermittent lactic acidemia": [ + "HP:0004913" + ], + "recurrent infantile hypoglycemia": [ + "HP:0004914" + ], + "episodic infantile hypoglycemia": [ + "HP:0004914" + ], + "recurrent low blood sugar in infant": [ + "HP:0004914" + ], + "impairment of galactose metabolism": [ + "HP:0004915" + ], + "impaired galactose metabolism": [ + "HP:0004915" + ], + "generalize distal tubular acidosis": [ + "HP:0004916" + ], + "generalized distal tubular acidosis": [ + "HP:0004916" + ], + "generalise distal tubular acidosis": [ + "HP:0004916" + ], + "generalised distal tubular acidosis": [ + "HP:0004916" + ], + "hyperchloremic metabolic acidosis": [ + "HP:0004918" + ], + "non - gap acidosis": [ + "HP:0004918" + ], + "galactose intolerance": [ + "HP:0004919" + ], + "phenylpyruvic acidemia": [ + "HP:0004920" + ], + "abnormal magnesium concentration": [ + "HP:0004921" + ], + "abnormal magnesium metabolism": [ + "HP:0004921" + ], + "abnormal mg concentration": [ + "HP:0004921" + ], + "abnormality of magnesium homeostasis": [ + "HP:0004921" + ], + "atypical hyperphenylalaninemia": [ + "HP:0004922" + ], + "hyperphenylalaninemia": [ + "HP:0004923" + ], + "abnormal oral glucose tolerance": [ + "HP:0004924" + ], + "abnormal glucose oral tolerance test": [ + "HP:0004924" + ], + "chronic lactic acidosis": [ + "HP:0004925" + ], + "orthostatic hypotension due to autonomic dysfunction": [ + "HP:0004926" + ], + "pulmonary artery dilatation": [ + "HP:0004927" + ], + "obsolete peripheral arterial stenosis": [ + "HP:0004928" + ], + "obsolete coronary atherosclerosis": [ + "HP:0004929" + ], + "abnormality of the pulmonary vasculature": [ + "HP:0004930" + ], + "abnormality of the lung blood vessel": [ + "HP:0004930" + ], + "abnormality of the lung blood vessels": [ + "HP:0004930" + ], + "arteriosclerosis of small cerebral artery": [ + "HP:0004931" + ], + "arteriosclerosis of small cerebral arteries": [ + "HP:0004931" + ], + "harden artery wall in small cerebral artery": [ + "HP:0004931" + ], + "hardened artery wall in small cerebral arteries": [ + "HP:0004931" + ], + "ascend aortic dissection": [ + "HP:0004933" + ], + "ascending aortic dissection": [ + "HP:0004933" + ], + "type a aortic dissection": [ + "HP:0004933" + ], + "vascular calcification": [ + "HP:0004934" + ], + "pulmonary artery atresia": [ + "HP:0004935" + ], + "pulmonary atresia": [ + "HP:0004935" + ], + "venous thrombosis": [ + "HP:0004936" + ], + "blood clot in vein": [ + "HP:0004936" + ], + "pulmonary artery aneurysm": [ + "HP:0004937" + ], + "tortuous cerebral artery": [ + "HP:0004938" + ], + "tortuous cerebral arteries": [ + "HP:0004938" + ], + "twisted cerebral artery": [ + "HP:0004938" + ], + "twisted cerebral arteries": [ + "HP:0004938" + ], + "generalize arterial calcification": [ + "HP:0004940" + ], + "generalized arterial calcification": [ + "HP:0004940" + ], + "generalise arterial calcification": [ + "HP:0004940" + ], + "generalised arterial calcification": [ + "HP:0004940" + ], + "extrahepatic portal hypertension": [ + "HP:0004941" + ], + "aortic aneurysm": [ + "HP:0004942" + ], + "aortic dilatation": [ + "HP:0004942" + ], + "bulge in wall of large artery that carry blood away from heart": [ + "HP:0004942" + ], + "bulge in wall of large artery that carries blood away from heart": [ + "HP:0004942" + ], + "accelerate atherosclerosis": [ + "HP:0004943" + ], + "accelerated atherosclerosis": [ + "HP:0004943" + ], + "accelerate plaque build - up in artery": [ + "HP:0004943" + ], + "accelerated plaque build - up in arteries": [ + "HP:0004943" + ], + "dilatation of the cerebral artery": [ + "HP:0004944" + ], + "brain aneurysm": [ + "HP:0004944" + ], + "cerebral aneurysm": [ + "HP:0004944" + ], + "cerebral artery aneurysm": [ + "HP:0004944" + ], + "intracranial aneurysm": [ + "HP:0004944" + ], + "extracranial internal carotid artery dissection": [ + "HP:0004945" + ], + "arteriovenous fistula": [ + "HP:0004947" + ], + "arteriovenous fistulas": [ + "HP:0004947" + ], + "vascular tortuosity": [ + "HP:0004948" + ], + "twist blood vessel": [ + "HP:0004948" + ], + "twisted blood vessels": [ + "HP:0004948" + ], + "peripheral arterial stenosis": [ + "HP:0004950" + ], + "arterial disease of leg": [ + "HP:0004950" + ], + "arterial disease of legs": [ + "HP:0004950" + ], + "occlusive arterial disease": [ + "HP:0004950" + ], + "occlusive vascular disease": [ + "HP:0004950" + ], + "peripheral artery disease": [ + "HP:0004950" + ], + "peripheral artery occlusive disease": [ + "HP:0004950" + ], + "peripheral vascular disease": [ + "HP:0004950" + ], + "pulmonary arteriovenous fistula": [ + "HP:0004952" + ], + "pulmonary arteriovenous fistulas": [ + "HP:0004952" + ], + "obsolete dilatation of abdominal aorta": [ + "HP:0004953" + ], + "obsolete dilatation of the descending aorta": [ + "HP:0004954" + ], + "generalize arterial tortuosity": [ + "HP:0004955" + ], + "generalized arterial tortuosity": [ + "HP:0004955" + ], + "arterial tortuosity , general": [ + "HP:0004955" + ], + "arterial tortuosity , generalise": [ + "HP:0004955" + ], + "arterial tortuosity , generalised": [ + "HP:0004955" + ], + "arterial tortuosity , generalize": [ + "HP:0004955" + ], + "arterial tortuosity , generalized": [ + "HP:0004955" + ], + "generalise arterial tortuosity": [ + "HP:0004955" + ], + "generalised arterial tortuosity": [ + "HP:0004955" + ], + "generalise twisted artery": [ + "HP:0004955" + ], + "generalised twisted arteries": [ + "HP:0004955" + ], + "generalize twisted artery": [ + "HP:0004955" + ], + "generalized twisted arteries": [ + "HP:0004955" + ], + "descend thoracic aorta aneurysm": [ + "HP:0004959" + ], + "descending thoracic aorta aneurysm": [ + "HP:0004959" + ], + "dilatation of the descend thoracic aorta": [ + "HP:0004959" + ], + "dilatation of the descending thoracic aorta": [ + "HP:0004959" + ], + "absent pulmonary artery": [ + "HP:0004960" + ], + "absent lung artery": [ + "HP:0004960" + ], + "miss pulmonary artery": [ + "HP:0004960" + ], + "missing pulmonary artery": [ + "HP:0004960" + ], + "pulmonary artery sling": [ + "HP:0004961" + ], + "thoracic aorta calcification": [ + "HP:0004962" + ], + "calcification of the aorta": [ + "HP:0004963" + ], + "pulmonary arterial medial hypertrophy": [ + "HP:0004964" + ], + "hypertrophy of the pulmonary artery wall": [ + "HP:0004964" + ], + "medial calcification of large artery": [ + "HP:0004966" + ], + "medial calcification of large arteries": [ + "HP:0004966" + ], + "recurrent cerebral hemorrhage": [ + "HP:0004968" + ], + "recurrent cerebral haemorrhage": [ + "HP:0004968" + ], + "recurrent hemorrhagic stroke": [ + "HP:0004968" + ], + "peripheral pulmonary artery stenosis": [ + "HP:0004969" + ], + "narrowing of peripheral lung artery": [ + "HP:0004969" + ], + "peripheral pulmonary stenosis": [ + "HP:0004969" + ], + "peripheral pulmonic stenosis": [ + "HP:0004969" + ], + "ascend tubular aorta aneurysm": [ + "HP:0004970" + ], + "ascending tubular aorta aneurysm": [ + "HP:0004970" + ], + "aneurysm of the ascend tubular aorta": [ + "HP:0004970" + ], + "aneurysm of the ascending tubular aorta": [ + "HP:0004970" + ], + "ascend aorta dilation": [ + "HP:0004970" + ], + "ascending aorta dilation": [ + "HP:0004970" + ], + "ascend aortic aneurysm": [ + "HP:0004970" + ], + "ascending aortic aneurysm": [ + "HP:0004970" + ], + "ascend aortic dilation": [ + "HP:0004970" + ], + "ascending aortic dilation": [ + "HP:0004970" + ], + "bulging of wall of large artery locate above heart": [ + "HP:0004970" + ], + "bulging of wall of large artery located above heart": [ + "HP:0004970" + ], + "dilatation of ascend aorta": [ + "HP:0004970" + ], + "dilatation of ascending aorta": [ + "HP:0004970" + ], + "pulmonary artery hypoplasia": [ + "HP:0004971" + ], + "underdeveloped lung artery": [ + "HP:0004971" + ], + "underdeveloped pulmonary artery": [ + "HP:0004971" + ], + "elevate mean arterial pressure": [ + "HP:0004972" + ], + "elevated mean arterial pressure": [ + "HP:0004972" + ], + "coarctation of abdominal aorta": [ + "HP:0004974" + ], + "erlenmeyer flask deformity of the femur": [ + "HP:0004975" + ], + "erlenmeyer flask deformity of the femurs": [ + "HP:0004975" + ], + "erlenmeyer flask deformity of distal femur": [ + "HP:0004975" + ], + "erlenmeyer flask femur": [ + "HP:0004975" + ], + "erlenmeyer flask femora": [ + "HP:0004975" + ], + "erlenmeyer flask shape thighbone": [ + "HP:0004975" + ], + "erlenmeyer flask shaped thighbone": [ + "HP:0004975" + ], + "knee dislocation": [ + "HP:0004976" + ], + "dislocation of the knee": [ + "HP:0004976" + ], + "dislocations of the knees": [ + "HP:0004976" + ], + "knee dislocations": [ + "HP:0004976" + ], + "bilateral radial aplasia": [ + "HP:0004977" + ], + "bilateral absence of radius": [ + "HP:0004977" + ], + "metaphyseal sclerosis": [ + "HP:0004979" + ], + "increase bone density in wide portion of long bone": [ + "HP:0004979" + ], + "increased bone density in wide portion of long bone": [ + "HP:0004979" + ], + "sclerotic metaphyses": [ + "HP:0004979" + ], + "metaphyseal rarefaction": [ + "HP:0004980" + ], + "rarefaction of the metaphyses": [ + "HP:0004980" + ], + "prominent styloid process of ulna": [ + "HP:0004981" + ], + "obsolete rudimentary to absent fibula": [ + "HP:0004986" + ], + "obsolete rudimentary to absent fibulae": [ + "HP:0004986" + ], + "mesomelic leg shorten": [ + "HP:0004987" + ], + "mesomelic leg shortening": [ + "HP:0004987" + ], + "mesomelia of the low limb": [ + "HP:0004987" + ], + "mesomelia of the lower limbs": [ + "HP:0004987" + ], + "mesomelic low limb shorten": [ + "HP:0004987" + ], + "mesomelic lower limb shortening": [ + "HP:0004987" + ], + "epiphyseal streak": [ + "HP:0004990" + ], + "epiphyseal streaking": [ + "HP:0004990" + ], + "rhizomelic arm shortening": [ + "HP:0004991" + ], + "slender long bone with narrow diaphysis": [ + "HP:0004993" + ], + "slender long bones with narrow diaphyses": [ + "HP:0004993" + ], + "slender long bone with narrow shaft": [ + "HP:0004993" + ], + "slender long bones with narrow shaft": [ + "HP:0004993" + ], + "multicentric ossification of proximal humeral epiphysis": [ + "HP:0004997" + ], + "multicentric ossification of proximal humeral epiphyses": [ + "HP:0004997" + ], + "recurrent patellar dislocation": [ + "HP:0005001" + ], + "recurrent dislocation of patella": [ + "HP:0005001" + ], + "recurrent dislocation of patellas": [ + "HP:0005001" + ], + "aplasia / hypoplasia of the capital femoral epiphysis": [ + "HP:0005003" + ], + "absent / small end part of innermost thighbone": [ + "HP:0005003" + ], + "absent / underdeveloped end part of innermost thighbone": [ + "HP:0005003" + ], + "flatten proximal radial epiphysis": [ + "HP:0005004" + ], + "flattened proximal radial epiphyses": [ + "HP:0005004" + ], + "femoral bow present at birth , straighten with time": [ + "HP:0005005" + ], + "femoral bowing present at birth , straightening with time": [ + "HP:0005005" + ], + "bowing of thighbone at birth , straighten with time": [ + "HP:0005005" + ], + "bowing of thighbone at birth , straightening with time": [ + "HP:0005005" + ], + "large joint dislocation": [ + "HP:0005008" + ], + "large joint dislocations": [ + "HP:0005008" + ], + "dumbbell - shape humerus": [ + "HP:0005009" + ], + "dumbbell - shaped humerus": [ + "HP:0005009" + ], + "dumbbell - shape long bone in upper arm": [ + "HP:0005009" + ], + "dumbbell - shaped long bone in upper arm": [ + "HP:0005009" + ], + "osteomyelitis lead to amputation due to slow healing fracture": [ + "HP:0005010" + ], + "osteomyelitis leading to amputation due to slow healing fractures": [ + "HP:0005010" + ], + "mesomelic arm shortening": [ + "HP:0005011" + ], + "mesomelia of the upper limb": [ + "HP:0005011" + ], + "mesomelia of the upper limbs": [ + "HP:0005011" + ], + "upper limb brachymesomelia": [ + "HP:0005011" + ], + "dysplastic distal radial epiphysis": [ + "HP:0005013" + ], + "dysplastic distal radial epiphyses": [ + "HP:0005013" + ], + "polyarticular chondrocalcinosis": [ + "HP:0005017" + ], + "diaphyseal thicken": [ + "HP:0005019" + ], + "diaphyseal thickening": [ + "HP:0005019" + ], + "thickening of shaft or central part of long bone": [ + "HP:0005019" + ], + "thickening of shaft or central part of long bones": [ + "HP:0005019" + ], + "bilateral elbow dislocation": [ + "HP:0005021" + ], + "bilateral elbow dislocations": [ + "HP:0005021" + ], + "dislocate elbow on both side": [ + "HP:0005021" + ], + "dislocated elbows on both sides": [ + "HP:0005021" + ], + "hypoplastic distal humerus": [ + "HP:0005025" + ], + "hypoplastic distal humeri": [ + "HP:0005025" + ], + "mesomelic / rhizomelic limb shorten": [ + "HP:0005026" + ], + "mesomelic / rhizomelic limb shortening": [ + "HP:0005026" + ], + "widen proximal tibial metaphyses": [ + "HP:0005028" + ], + "widened proximal tibial metaphyses": [ + "HP:0005028" + ], + "wide innermost wide portion of shankbone bone": [ + "HP:0005028" + ], + "wide innermost wide portion of shinbone bone": [ + "HP:0005028" + ], + "distal ulnar hypoplasia": [ + "HP:0005033" + ], + "distal shortening of ulna": [ + "HP:0005033" + ], + "hypoplastic distal ulna": [ + "HP:0005033" + ], + "shortening of all phalanx of the toe": [ + "HP:0005035" + ], + "shortening of all phalanges of the toes": [ + "HP:0005035" + ], + "short toe bone": [ + "HP:0005035" + ], + "short toe bones": [ + "HP:0005035" + ], + "unilateral ulnar hypoplasia": [ + "HP:0005036" + ], + "proximal radio - ulnar synostosis": [ + "HP:0005037" + ], + "multiple long - bone exostosis": [ + "HP:0005039" + ], + "multiple long - bone exostoses": [ + "HP:0005039" + ], + "multiple exostosis of long tubular bone": [ + "HP:0005039" + ], + "multiple exostoses of long tubular bones": [ + "HP:0005039" + ], + "irregular capital femoral epiphysis": [ + "HP:0005041" + ], + "irregular capital femoral epiphyses": [ + "HP:0005041" + ], + "irregular end part of innermost thighbone": [ + "HP:0005041" + ], + "irregular proximal femoral epiphysis": [ + "HP:0005041" + ], + "irregular proximal femoral epiphyses": [ + "HP:0005041" + ], + "irregular , rachitic - like metaphyses": [ + "HP:0005042" + ], + "proximal humeral metaphyseal irregularity": [ + "HP:0005043" + ], + "irregular proximal humeral metaphyses": [ + "HP:0005043" + ], + "diaphyseal cortical sclerosis": [ + "HP:0005045" + ], + "synostosis of carpal bone": [ + "HP:0005048" + ], + "synostosis of carpal bones": [ + "HP:0005048" + ], + "fusion of wrist bone": [ + "HP:0005048" + ], + "fusion of wrist bones": [ + "HP:0005048" + ], + "anterolateral radial head dislocation": [ + "HP:0005050" + ], + "anterior / lateral radial head dislocation": [ + "HP:0005050" + ], + "metaphyseal spur": [ + "HP:0005054" + ], + "metaphyseal spurs": [ + "HP:0005054" + ], + "arthralgia / arthritis": [ + "HP:0005059" + ], + "joint pain / joint inflammation": [ + "HP:0005059" + ], + "limited elbow flexion / extension": [ + "HP:0005060" + ], + "fragment , irregular epiphysis": [ + "HP:0005063" + ], + "fragmented , irregular epiphyses": [ + "HP:0005063" + ], + "fragment , irregular end part of bone": [ + "HP:0005063" + ], + "fragmented , irregular end part of bone": [ + "HP:0005063" + ], + "cone - shaped epiphysis fuse within their metaphyses": [ + "HP:0005066" + ], + "cone - shaped epiphyses fused within their metaphyses": [ + "HP:0005066" + ], + "cone - shaped end part of long bone fuse within their wide portion of wide bone": [ + "HP:0005066" + ], + "cone - shaped end part of long bone fused within their wide portion of wide bone": [ + "HP:0005066" + ], + "proximal fibular overgrowth": [ + "HP:0005067" + ], + "overgrowth of innermost part of calf bone": [ + "HP:0005067" + ], + "absent styloid process of ulna": [ + "HP:0005068" + ], + "rhizo - meso - acromelic limb shorten": [ + "HP:0005069" + ], + "rhizo - meso - acromelic limb shortening": [ + "HP:0005069" + ], + "proximal radial head dislocation": [ + "HP:0005070" + ], + "hyperextensibility at wrist": [ + "HP:0005072" + ], + "hyperextensibility at wrists": [ + "HP:0005072" + ], + "increase laxity of wrist": [ + "HP:0005072" + ], + "increased laxity of wrists": [ + "HP:0005072" + ], + "increase wrist mobility": [ + "HP:0005072" + ], + "increased wrist mobility": [ + "HP:0005072" + ], + "anterior radial head dislocation": [ + "HP:0005084" + ], + "anterior dislocation of radial head": [ + "HP:0005084" + ], + "limited knee flexion / extension": [ + "HP:0005085" + ], + "knee osteoarthritis": [ + "HP:0005086" + ], + "abnormal metaphyseal trabeculation": [ + "HP:0005089" + ], + "lateral femoral bowing": [ + "HP:0005090" + ], + "streaky metaphyseal sclerosis": [ + "HP:0005092" + ], + "streak increase in bone density in wide portion of wide bone": [ + "HP:0005092" + ], + "absent proximal radial epiphysis": [ + "HP:0005093" + ], + "absent proximal radial epiphyses": [ + "HP:0005093" + ], + "distal femoral bowing": [ + "HP:0005096" + ], + "severe hydrops fetalis": [ + "HP:0005099" + ], + "severe hydrops": [ + "HP:0005099" + ], + "premature birth follow premature rupture of fetal membrane": [ + "HP:0005100" + ], + "premature birth following premature rupture of fetal membranes": [ + "HP:0005100" + ], + "premature birth follow premature rupture of foetal membrane": [ + "HP:0005100" + ], + "premature birth following premature rupture of foetal membranes": [ + "HP:0005100" + ], + "high - frequency hearing impairment": [ + "HP:0005101" + ], + "hearing loss , high - frequency": [ + "HP:0005101" + ], + "high frequency hearing loss": [ + "HP:0005101" + ], + "high - frequency deafness": [ + "HP:0005101" + ], + "progressive high frequency hearing loss": [ + "HP:0005101" + ], + "progressive high - frequency hearing loss": [ + "HP:0005101" + ], + "cochlear degeneration": [ + "HP:0005102" + ], + "progressive cochlear degeneration": [ + "HP:0005102" + ], + "calcification of the auricular cartilage": [ + "HP:0005103" + ], + "cartilaginous ossification of pinna": [ + "HP:0005103" + ], + "cartilaginous ossification of pinnae": [ + "HP:0005103" + ], + "ear cartilage calcification": [ + "HP:0005103" + ], + "ossification of pinna": [ + "HP:0005103" + ], + "ossification of pinnae": [ + "HP:0005103" + ], + "petrified ear": [ + "HP:0005103" + ], + "hypoplastic nasal septum": [ + "HP:0005104" + ], + "decreased size of nasal septum": [ + "HP:0005104" + ], + "decreased size of septum of nose": [ + "HP:0005104" + ], + "hypoplasia of septum of nose": [ + "HP:0005104" + ], + "small nasal septum": [ + "HP:0005104" + ], + "small septum of nose": [ + "HP:0005104" + ], + "abnormal nasal morphology": [ + "HP:0005105" + ], + "abnormal nose morphology": [ + "HP:0005105" + ], + "abnormal of morphology of nose": [ + "HP:0005105" + ], + "abnormal of nasal shape": [ + "HP:0005105" + ], + "abnormal of shape of nose": [ + "HP:0005105" + ], + "abnormality of the vertebral endplate": [ + "HP:0005106" + ], + "abnormality of the vertebral endplates": [ + "HP:0005106" + ], + "abnormal sacrum morphology": [ + "HP:0005107" + ], + "abnormality of the sacrum": [ + "HP:0005107" + ], + "abnormality of the intervertebral disk": [ + "HP:0005108" + ], + "abnormality of the intervertebral disc": [ + "HP:0005108" + ], + "abnormality of the achilles tendon": [ + "HP:0005109" + ], + "abnormality of the calcaneal tendon": [ + "HP:0005109" + ], + "atrial fibrillation": [ + "HP:0005110" + ], + "quiver upper heart chamber result in irregular heartbeat": [ + "HP:0005110" + ], + "quivering upper heart chambers resulting in irregular heartbeat": [ + "HP:0005110" + ], + "obsolete dilatation of the ascending aorta": [ + "HP:0005111" + ], + "abdominal aortic aneurysm": [ + "HP:0005112" + ], + "dilatation of the abdominal aorta": [ + "HP:0005112" + ], + "aortic arch aneurysm": [ + "HP:0005113" + ], + "aortic arch dilatation": [ + "HP:0005113" + ], + "dilatation of the aortic arch": [ + "HP:0005113" + ], + "obsolete abnormality of the peripheral artery": [ + "HP:0005114" + ], + "obsolete abnormalities of the peripheral arteries": [ + "HP:0005114" + ], + "supraventricular arrhythmia": [ + "HP:0005115" + ], + "arrhythmia , supraventricular": [ + "HP:0005115" + ], + "arrhythmias , supraventricular": [ + "HP:0005115" + ], + "arterial tortuosity": [ + "HP:0005116" + ], + "elevate diastolic blood pressure": [ + "HP:0005117" + ], + "elevated diastolic blood pressure": [ + "HP:0005117" + ], + "elevate diastolic bp": [ + "HP:0005117" + ], + "elevated diastolic bp": [ + "HP:0005117" + ], + "abnormal cardiac atrium morphology": [ + "HP:0005120" + ], + "abnormality of cardiac atrium morphology": [ + "HP:0005120" + ], + "abnormality of heart atrium": [ + "HP:0005120" + ], + "posterior scalloping of vertebral body": [ + "HP:0005121" + ], + "posterior scalloping of vertebral bodies": [ + "HP:0005121" + ], + "posterior vertebral body scallop": [ + "HP:0005121" + ], + "posterior vertebral body scalloping": [ + "HP:0005121" + ], + "congenital hypertrophy of left ventricle": [ + "HP:0005129" + ], + "obsolete restrictive heart failure": [ + "HP:0005130" + ], + "pericardial constriction": [ + "HP:0005132" + ], + "right ventricular dilatation": [ + "HP:0005133" + ], + "dilate heart right ventricle": [ + "HP:0005133" + ], + "dilated heart right ventricle": [ + "HP:0005133" + ], + "absence of the pulmonary valve": [ + "HP:0005134" + ], + "absent pulmonary valve": [ + "HP:0005134" + ], + "abnormal t - wave": [ + "HP:0005135" + ], + "ekg : t - wave abnormality": [ + "HP:0005135" + ], + "ekg : t - wave abnormalities": [ + "HP:0005135" + ], + "t - wave abnormality": [ + "HP:0005135" + ], + "t - wave abnormalities": [ + "HP:0005135" + ], + "mitral annular calcification": [ + "HP:0005136" + ], + "premature calcification of mitral annulus": [ + "HP:0005136" + ], + "obsolete episode of ventricular tachycardia": [ + "HP:0005141" + ], + "obsolete episodes of ventricular tachycardia": [ + "HP:0005141" + ], + "anomalous origin of right pulmonary artery from ascend aorta": [ + "HP:0005143" + ], + "anomalous origin of right pulmonary artery from ascending aorta": [ + "HP:0005143" + ], + "ventricular septal hypertrophy": [ + "HP:0005144" + ], + "thicken interventricular septum": [ + "HP:0005144" + ], + "thickened interventricular septum": [ + "HP:0005144" + ], + "coronary artery stenosis": [ + "HP:0005145" + ], + "narrowing of coronary artery": [ + "HP:0005145" + ], + "cardiac valve calcification": [ + "HP:0005146" + ], + "calcification of the cardiac valve": [ + "HP:0005146" + ], + "calcifications of the cardiac valves": [ + "HP:0005146" + ], + "bidirectional ventricular ectopy": [ + "HP:0005147" + ], + "pulmonary valve defect": [ + "HP:0005148" + ], + "pulmonary valve defects": [ + "HP:0005148" + ], + "abnormal atrioventricular conduction": [ + "HP:0005150" + ], + "preductal coarctation of the aorta": [ + "HP:0005151" + ], + "proximal aortic coarctation": [ + "HP:0005151" + ], + "histiocytoid cardiomyopathy": [ + "HP:0005152" + ], + "arachnocytosis of the myocardium": [ + "HP:0005152" + ], + "foamy myocardial transformation": [ + "HP:0005152" + ], + "focal lipid cardiomyopathy": [ + "HP:0005152" + ], + "infantile cardiomyopathy with histiocytoid change": [ + "HP:0005152" + ], + "infantile cardiomyopathy with histiocytoid changes": [ + "HP:0005152" + ], + "infantile xanthomatous cardiomyopathy": [ + "HP:0005152" + ], + "isolated cardiac lipidosis": [ + "HP:0005152" + ], + "myocardial or conduction system hamartoma": [ + "HP:0005152" + ], + "oncocytic cardiomyopathy": [ + "HP:0005152" + ], + "ventricular escape rhythm": [ + "HP:0005155" + ], + "idioventricular escape rhythm": [ + "HP:0005155" + ], + "hypoplastic leave atrium": [ + "HP:0005156" + ], + "hypoplastic left atrium": [ + "HP:0005156" + ], + "left atrium hypoplasia": [ + "HP:0005156" + ], + "underdeveloped leave heart atrium": [ + "HP:0005156" + ], + "underdeveloped left heart atrium": [ + "HP:0005156" + ], + "concentric hypertrophic cardiomyopathy": [ + "HP:0005157" + ], + "symmetric , concentric , hypertrophic cardiomyopathy": [ + "HP:0005157" + ], + "total anomalous pulmonary venous return": [ + "HP:0005160" + ], + "total anomalous pulmonary venous connection": [ + "HP:0005160" + ], + "total anomalous pulmonary venous drainage": [ + "HP:0005160" + ], + "abnormal leave ventricular function": [ + "HP:0005162" + ], + "abnormal left ventricular function": [ + "HP:0005162" + ], + "impaired leave ventricular function": [ + "HP:0005162" + ], + "impaired left ventricular function": [ + "HP:0005162" + ], + "leave ventricular dysfunction": [ + "HP:0005162" + ], + "left ventricular dysfunction": [ + "HP:0005162" + ], + "leave ventricular failure": [ + "HP:0005162" + ], + "left ventricular failure": [ + "HP:0005162" + ], + "leave ventricular impairment": [ + "HP:0005162" + ], + "left ventricular impairment": [ + "HP:0005162" + ], + "left - side heart failure": [ + "HP:0005162" + ], + "left - sided heart failure": [ + "HP:0005162" + ], + "dysplastic pulmonary valve": [ + "HP:0005164" + ], + "shorten pr interval": [ + "HP:0005165" + ], + "shortened pr interval": [ + "HP:0005165" + ], + "electrocardiographic short pr interval": [ + "HP:0005165" + ], + "short p - r interval": [ + "HP:0005165" + ], + "shorten pr interval on ekg": [ + "HP:0005165" + ], + "shortened pr interval on ekg": [ + "HP:0005165" + ], + "elevate right atrial pressure": [ + "HP:0005168" + ], + "elevated right atrial pressure": [ + "HP:0005168" + ], + "complete heart block with broad qrs complex": [ + "HP:0005170" + ], + "complete heart block with broad qrs complexes": [ + "HP:0005170" + ], + "leave posterior fascicular block": [ + "HP:0005172" + ], + "left posterior fascicular block": [ + "HP:0005172" + ], + "leave posterior hemiblock": [ + "HP:0005172" + ], + "left posterior hemiblock": [ + "HP:0005172" + ], + "obsolete calcific aortic valve stenosis": [ + "HP:0005173" + ], + "membranous subvalvular aortic stenosis": [ + "HP:0005174" + ], + "dysplastic aortic valve": [ + "HP:0005176" + ], + "premature arteriosclerosis": [ + "HP:0005177" + ], + "premature hardening of artery": [ + "HP:0005177" + ], + "premature hardening of arteries": [ + "HP:0005177" + ], + "complete heart block with narrow qrs complex": [ + "HP:0005178" + ], + "complete heart block with narrow qrs complexes": [ + "HP:0005178" + ], + "tricuspid regurgitation": [ + "HP:0005180" + ], + "tricuspid insufficiency": [ + "HP:0005180" + ], + "tricuspid valve regurgitation": [ + "HP:0005180" + ], + "premature coronary artery atherosclerosis": [ + "HP:0005181" + ], + "premature coronary artery disease": [ + "HP:0005181" + ], + "bicuspid pulmonary valve": [ + "HP:0005182" + ], + "pericardial lymphangiectasia": [ + "HP:0005183" + ], + "prolonged qtc interval": [ + "HP:0005184" + ], + "global systolic dysfunction": [ + "HP:0005185" + ], + "synovial hypertrophy": [ + "HP:0005186" + ], + "progressive joint destruction": [ + "HP:0005187" + ], + "proximal finger joint hyperextensibility": [ + "HP:0005190" + ], + "congenital knee dislocation": [ + "HP:0005191" + ], + "dislocate knee since birth": [ + "HP:0005191" + ], + "dislocated knee since birth": [ + "HP:0005191" + ], + "restrict large joint movement": [ + "HP:0005193" + ], + "restricted large joint movement": [ + "HP:0005193" + ], + "flatten metatarsal head": [ + "HP:0005194" + ], + "flattened metatarsal heads": [ + "HP:0005194" + ], + "flatten head of long bone of foot": [ + "HP:0005194" + ], + "flattened head of long bone of foot": [ + "HP:0005194" + ], + "polyarticular arthropathy": [ + "HP:0005195" + ], + "generalize morning stiffness": [ + "HP:0005197" + ], + "generalized morning stiffness": [ + "HP:0005197" + ], + "generalise morning stiffness": [ + "HP:0005197" + ], + "generalised morning stiffness": [ + "HP:0005197" + ], + "stiff interphalangeal joint": [ + "HP:0005198" + ], + "stiff interphalangeal joints": [ + "HP:0005198" + ], + "stiff hinge joint": [ + "HP:0005198" + ], + "stiff hinge joints": [ + "HP:0005198" + ], + "aplasia of the abdominal wall musculature": [ + "HP:0005199" + ], + "absent abdominal musculature": [ + "HP:0005199" + ], + "retroperitoneal fibrosis": [ + "HP:0005200" + ], + "anomalous splenoportal venous system": [ + "HP:0005201" + ], + "helicobacter pylorus infection": [ + "HP:0005202" + ], + "helicobacter pylori infection": [ + "HP:0005202" + ], + "spontaneous esophageal perforation": [ + "HP:0005203" + ], + "boerhaave syndrome": [ + "HP:0005203" + ], + "spontaneous esophageal rupture": [ + "HP:0005203" + ], + "pancreatic pseudocyst": [ + "HP:0005206" + ], + "gastric hypertrophy": [ + "HP:0005207" + ], + "increase stomach size": [ + "HP:0005207" + ], + "increased stomach size": [ + "HP:0005207" + ], + "secretory diarrhea": [ + "HP:0005208" + ], + "secretory diarrhoea": [ + "HP:0005208" + ], + "intrahepatic bile duct cyst": [ + "HP:0005209" + ], + "intrahepatic bile duct cysts": [ + "HP:0005209" + ], + "hypoplastic colon": [ + "HP:0005210" + ], + "hypoplasia of the colon": [ + "HP:0005210" + ], + "underdeveloped colon": [ + "HP:0005210" + ], + "midgut malrotation": [ + "HP:0005211" + ], + "anal mucosal leukoplakia": [ + "HP:0005212" + ], + "pancreatic calcification": [ + "HP:0005213" + ], + "pancreatic calcifications": [ + "HP:0005213" + ], + "intestinal obstruction": [ + "HP:0005214" + ], + "bowel obstruction": [ + "HP:0005214" + ], + "intestinal blockage": [ + "HP:0005214" + ], + "frequent giardia lamblia infestation": [ + "HP:0005215" + ], + "impaired mastication": [ + "HP:0005216" + ], + "chew difficulty": [ + "HP:0005216" + ], + "chewing difficulties": [ + "HP:0005216" + ], + "chewing difficulty": [ + "HP:0005216" + ], + "difficulty chew": [ + "HP:0005216" + ], + "difficulty chewing": [ + "HP:0005216" + ], + "duplication of internal organ": [ + "HP:0005217" + ], + "duplication of internal organs": [ + "HP:0005217" + ], + "anoperineal fistula": [ + "HP:0005218" + ], + "perianal fistula": [ + "HP:0005218" + ], + "absence of intrinsic factor": [ + "HP:0005219" + ], + "intrinsic factor absent from gastric juice": [ + "HP:0005219" + ], + "multiple intestinal neurofibromatosis": [ + "HP:0005220" + ], + "bowel diverticulosis": [ + "HP:0005222" + ], + "bowel diverticulum": [ + "HP:0005222" + ], + "bowel diverticula": [ + "HP:0005222" + ], + "duplicate colon": [ + "HP:0005223" + ], + "duplicated colon": [ + "HP:0005223" + ], + "rectal abscess": [ + "HP:0005224" + ], + "perirectal abscess": [ + "HP:0005224" + ], + "intestinal edema": [ + "HP:0005225" + ], + "intestinal oedema": [ + "HP:0005225" + ], + "adenomatous colonic polyposis": [ + "HP:0005227" + ], + "multiple adenomatous colon polyp": [ + "HP:0005227" + ], + "multiple adenomatous colon polyps": [ + "HP:0005227" + ], + "multiple colonic adenomatous polyp": [ + "HP:0005227" + ], + "multiple colonic adenomatous polyps": [ + "HP:0005227" + ], + "jejunoileal ulceration": [ + "HP:0005229" + ], + "biliary tract obstruction": [ + "HP:0005230" + ], + "chronic gastritis": [ + "HP:0005231" + ], + "pancreatic dysplasia": [ + "HP:0005232" + ], + "hypoplasia of the gallbladder": [ + "HP:0005233" + ], + "hypoplastic gallbladder": [ + "HP:0005233" + ], + "neonatal intestinal obstruction": [ + "HP:0005234" + ], + "jejunal atresia": [ + "HP:0005235" + ], + "chronic calcifying pancreatitis": [ + "HP:0005236" + ], + "degenerative liver disease": [ + "HP:0005237" + ], + "discrete intestinal polyp": [ + "HP:0005238" + ], + "discrete intestinal polyps": [ + "HP:0005238" + ], + "esophageal obstruction": [ + "HP:0005240" + ], + "total intestinal aganglionosis": [ + "HP:0005241" + ], + "extrahepatic biliary duct atresia": [ + "HP:0005242" + ], + "biliary atresia , extrahepatic": [ + "HP:0005242" + ], + "partial abdominal muscle agenesis": [ + "HP:0005243" + ], + "gastrointestinal infarction": [ + "HP:0005244" + ], + "gastrointestinal infarctions": [ + "HP:0005244" + ], + "death of digestive organ tissue due to poor blood supply": [ + "HP:0005244" + ], + "gi infarction": [ + "HP:0005244" + ], + "gi infarctions": [ + "HP:0005244" + ], + "intestinal hypoplasia": [ + "HP:0005245" + ], + "hypoplastic intestine": [ + "HP:0005245" + ], + "hypoplastic intestines": [ + "HP:0005245" + ], + "underdeveloped instestine": [ + "HP:0005245" + ], + "giant hypertrophic gastritis": [ + "HP:0005246" + ], + "menetrier disease": [ + "HP:0005246" + ], + "hypoplasia of the abdominal wall musculature": [ + "HP:0005247" + ], + "abdominal muscular hypoplasia": [ + "HP:0005247" + ], + "intrahepatic biliary atresia": [ + "HP:0005248" + ], + "bile duct paucity": [ + "HP:0005248" + ], + "intrahepatic atresia of biliary duct": [ + "HP:0005248" + ], + "functional intestinal obstruction": [ + "HP:0005249" + ], + "high intestinal obstruction": [ + "HP:0005250" + ], + "increase anterioposterior diameter of thorax": [ + "HP:0005253" + ], + "increased anterioposterior diameter of thorax": [ + "HP:0005253" + ], + "increase anterioposterior diameter of chest": [ + "HP:0005253" + ], + "increased anterioposterior diameter of chest": [ + "HP:0005253" + ], + "unilateral chest hypoplasia": [ + "HP:0005254" + ], + "small chest on one side": [ + "HP:0005254" + ], + "underdeveloped chest on one side": [ + "HP:0005254" + ], + "absence of pectoralis minor muscle": [ + "HP:0005255" + ], + "pectoralis minor aplasia": [ + "HP:0005255" + ], + "unilateral absence of pectoralis major muscle": [ + "HP:0005256" + ], + "unilateral aplasia of pectoralis major muscle": [ + "HP:0005256" + ], + "thoracic hypoplasia": [ + "HP:0005257" + ], + "small chest": [ + "HP:0005257" + ], + "small thorax": [ + "HP:0005257" + ], + "pectoral muscle hypoplasia / aplasia": [ + "HP:0005258" + ], + "small / absent pec muscle": [ + "HP:0005258" + ], + "underdeveloped / absent pec muscle": [ + "HP:0005258" + ], + "abnormal facility in oppose the shoulder": [ + "HP:0005259" + ], + "abnormal facility in opposing the shoulders": [ + "HP:0005259" + ], + "joint hemorrhage": [ + "HP:0005261" + ], + "bleed within a joint": [ + "HP:0005261" + ], + "bleeding within a joint": [ + "HP:0005261" + ], + "hemarthroses": [ + "HP:0005261" + ], + "hemarthrosis": [ + "HP:0005261" + ], + "joint haemorrhage": [ + "HP:0005261" + ], + "spontaneous joint haemorrhage": [ + "HP:0005261" + ], + "spontaneous joint hemorrhage": [ + "HP:0005261" + ], + "abnormality of the synovia": [ + "HP:0005262" + ], + "gastritis": [ + "HP:0005263" + ], + "stomach inflammation": [ + "HP:0005263" + ], + "abnormality of the gallbladder": [ + "HP:0005264" + ], + "anomaly of the gallbladder": [ + "HP:0005264" + ], + "abnormal jejunum morphology": [ + "HP:0005265" + ], + "abnormality of the jejunum": [ + "HP:0005265" + ], + "intestinal polyp": [ + "HP:0005266" + ], + "intestinal polyps": [ + "HP:0005266" + ], + "premature delivery because of cervical insufficiency or membrane fragility": [ + "HP:0005267" + ], + "spontaneous abortion": [ + "HP:0005268" + ], + "miscarriage": [ + "HP:0005268" + ], + "prominent nasolabial fold": [ + "HP:0005272" + ], + "deep laugh line": [ + "HP:0005272" + ], + "deep laugh lines": [ + "HP:0005272" + ], + "deep nasolabial crease": [ + "HP:0005272" + ], + "deep nasolabial fold": [ + "HP:0005272" + ], + "deep nasolabial groove": [ + "HP:0005272" + ], + "deep smile line": [ + "HP:0005272" + ], + "deep smile lines": [ + "HP:0005272" + ], + "nasolabial crease , prominent": [ + "HP:0005272" + ], + "prominent laugh line": [ + "HP:0005272" + ], + "prominent laugh lines": [ + "HP:0005272" + ], + "prominent nasolabial groove": [ + "HP:0005272" + ], + "prominent smile line": [ + "HP:0005272" + ], + "prominent smile lines": [ + "HP:0005272" + ], + "absent nasal septal cartilage": [ + "HP:0005273" + ], + "absent nasal septum": [ + "HP:0005273" + ], + "ageneis of nasal septal cartilage": [ + "HP:0005273" + ], + "failure of development of nasal septal cartilage": [ + "HP:0005273" + ], + "prominent nasal tip": [ + "HP:0005274" + ], + "bulbous tip of nose": [ + "HP:0005274" + ], + "hyperplasia of nasal tip": [ + "HP:0005274" + ], + "hyperplasia of tip of nose": [ + "HP:0005274" + ], + "hypertrophy of nasal tip": [ + "HP:0005274" + ], + "hypertrophy of tip of nose": [ + "HP:0005274" + ], + "large nasal tip": [ + "HP:0005274" + ], + "large tip of nose": [ + "HP:0005274" + ], + "prominent tip of nose": [ + "HP:0005274" + ], + "pronounce nasal tip": [ + "HP:0005274" + ], + "pronounced nasal tip": [ + "HP:0005274" + ], + "pronounced tip of nose": [ + "HP:0005274" + ], + "cartilaginous ossification of nose": [ + "HP:0005275" + ], + "cartilaginous nasal ossification": [ + "HP:0005275" + ], + "hypoplastic nasal tip": [ + "HP:0005278" + ], + "aplasia of nasal tip": [ + "HP:0005278" + ], + "decreased size of nasal tip": [ + "HP:0005278" + ], + "decreased size of tip of nose": [ + "HP:0005278" + ], + "deficient nasal tip": [ + "HP:0005278" + ], + "hypoplasia of tip of nose": [ + "HP:0005278" + ], + "hypotrophic nasal tip": [ + "HP:0005278" + ], + "hypotrophic tip of nose": [ + "HP:0005278" + ], + "small nasal tip": [ + "HP:0005278" + ], + "small tip of nose": [ + "HP:0005278" + ], + "underdevelopment of nasal tip": [ + "HP:0005278" + ], + "underdevelopment of tip of nose": [ + "HP:0005278" + ], + "depress nasal bridge": [ + "HP:0005280" + ], + "depressed nasal bridge": [ + "HP:0005280" + ], + "concave bridge of nose": [ + "HP:0005280" + ], + "concave nasal bridge": [ + "HP:0005280" + ], + "depressed bridge of nose": [ + "HP:0005280" + ], + "depress nasal root": [ + "HP:0005280" + ], + "depressed nasal root": [ + "HP:0005280" + ], + "depress nasal root / bridge": [ + "HP:0005280" + ], + "depressed nasal root / bridge": [ + "HP:0005280" + ], + "flat bridge of nose": [ + "HP:0005280" + ], + "flat nasal bridge": [ + "HP:0005280" + ], + "flat nasal root": [ + "HP:0005280" + ], + "flat , nasal bridge": [ + "HP:0005280" + ], + "flatten nasal bridge": [ + "HP:0005280" + ], + "flattened nasal bridge": [ + "HP:0005280" + ], + "low nasal bridge": [ + "HP:0005280" + ], + "low nasal root": [ + "HP:0005280" + ], + "retruded bridge of nose": [ + "HP:0005280" + ], + "retruded nasal bridge": [ + "HP:0005280" + ], + "hypoplastic nasal bridge": [ + "HP:0005281" + ], + "decreased size of bridge of nose": [ + "HP:0005281" + ], + "decreased size of nasal bridge": [ + "HP:0005281" + ], + "hypoplastic bridge of nose": [ + "HP:0005281" + ], + "hypotrophic bridge of nose": [ + "HP:0005281" + ], + "hypotrophic nasal bridge": [ + "HP:0005281" + ], + "small bridge of nose": [ + "HP:0005281" + ], + "small nasal bridge": [ + "HP:0005281" + ], + "absent nasal bridge": [ + "HP:0005285" + ], + "absent bridge of nose": [ + "HP:0005285" + ], + "agenesis of bridge of nose": [ + "HP:0005285" + ], + "agenesis of nasal bridge": [ + "HP:0005285" + ], + "miss bridge of nose": [ + "HP:0005285" + ], + "missing bridge of nose": [ + "HP:0005285" + ], + "miss nasal bridge": [ + "HP:0005285" + ], + "missing nasal bridge": [ + "HP:0005285" + ], + "abnormality of the naris": [ + "HP:0005288" + ], + "abnormality of the nares": [ + "HP:0005288" + ], + "abnormality of the nostril": [ + "HP:0005288" + ], + "abnormality of the nostrils": [ + "HP:0005288" + ], + "anomaly of the naris": [ + "HP:0005288" + ], + "anomaly of the nares": [ + "HP:0005288" + ], + "deformity of the naris": [ + "HP:0005288" + ], + "deformity of the nares": [ + "HP:0005288" + ], + "deformity of the nostril": [ + "HP:0005288" + ], + "deformity of the nostrils": [ + "HP:0005288" + ], + "malformation of the naris": [ + "HP:0005288" + ], + "malformation of the nares": [ + "HP:0005288" + ], + "malformation of the nostril": [ + "HP:0005288" + ], + "malformation of the nostrils": [ + "HP:0005288" + ], + "abnormality of the nasolabial region": [ + "HP:0005289" + ], + "anomaly of the nasolabial region": [ + "HP:0005289" + ], + "deformity of the nasolabial region": [ + "HP:0005289" + ], + "malformation of the nasolabial region": [ + "HP:0005289" + ], + "internal carotid artery hypoplasia": [ + "HP:0005290" + ], + "aplasia of internal carotid artery": [ + "HP:0005290" + ], + "decreased size of internal carotid artery": [ + "HP:0005290" + ], + "deficiency of internal carotid artery": [ + "HP:0005290" + ], + "hypotrophic internal carotid artery": [ + "HP:0005290" + ], + "small internal carotid artery": [ + "HP:0005290" + ], + "inflammatory arteriopathy": [ + "HP:0005291" + ], + "intimal thickening in the coronary artery": [ + "HP:0005292" + ], + "intimal thickening in the coronary arteries": [ + "HP:0005292" + ], + "venous insufficiency": [ + "HP:0005293" + ], + "poorly functioning vein": [ + "HP:0005293" + ], + "poorly functioning veins": [ + "HP:0005293" + ], + "arterial dissection": [ + "HP:0005294" + ], + "pseudocoarctation of the aorta": [ + "HP:0005295" + ], + "obsolete occlusive vascular disease": [ + "HP:0005296" + ], + "premature occlusive vascular stenosis": [ + "HP:0005297" + ], + "obsolete atrioventricular canal defect with right ventricle aorta and pulmonary atresia": [ + "HP:0005298" + ], + "obsolete premature peripheral vascular disease": [ + "HP:0005299" + ], + "nodular inflammatory vasculitis": [ + "HP:0005300" + ], + "persistent leave superior vena cava": [ + "HP:0005301" + ], + "persistent left superior vena cava": [ + "HP:0005301" + ], + "carotid artery tortuosity": [ + "HP:0005302" + ], + "tortuous carotid artery": [ + "HP:0005302" + ], + "tortuous carotid arteries": [ + "HP:0005302" + ], + "aortic arch calcification": [ + "HP:0005303" + ], + "hypoplastic pulmonary vein": [ + "HP:0005304" + ], + "hypoplastic pulmonary veins": [ + "HP:0005304" + ], + "underdeveloped lung vein": [ + "HP:0005304" + ], + "underdeveloped lung veins": [ + "HP:0005304" + ], + "cerebral venous thrombosis": [ + "HP:0005305" + ], + "blood clot in cerebral vein": [ + "HP:0005305" + ], + "cerebral thrombosis": [ + "HP:0005305" + ], + "cerebral vein thrombosis": [ + "HP:0005305" + ], + "capillary hemangioma": [ + "HP:0005306" + ], + "strawberry birthmark": [ + "HP:0005306" + ], + "postural hypotension with compensatory tachycardia": [ + "HP:0005307" + ], + "pulmonary artery vasoconstriction": [ + "HP:0005308" + ], + "obsolete peripheral vascular insufficiency": [ + "HP:0005309" + ], + "large vessel vasculitis": [ + "HP:0005310" + ], + "agenesis of pulmonary vessel": [ + "HP:0005311" + ], + "agenesis of pulmonary vessels": [ + "HP:0005311" + ], + "absent lung vessel": [ + "HP:0005311" + ], + "absent lung vessels": [ + "HP:0005311" + ], + "pulmonary aterial intimal fibrosis": [ + "HP:0005312" + ], + "arterial fibromuscular dysplasia": [ + "HP:0005313" + ], + "anomalous branch of internal carotid artery": [ + "HP:0005314" + ], + "anomalous branches of internal carotid artery": [ + "HP:0005314" + ], + "obsolete peripheral artery occlusive disease": [ + "HP:0005315" + ], + "peripheral pulmonary vessel aplasia": [ + "HP:0005316" + ], + "increase pulmonary vascular resistance": [ + "HP:0005317" + ], + "increased pulmonary vascular resistance": [ + "HP:0005317" + ], + "cerebral vasculitis": [ + "HP:0005318" + ], + "lack of facial subcutaneous fat": [ + "HP:0005320" + ], + "lack of facial fat below the skin": [ + "HP:0005320" + ], + "mandibulofacial dysostosis": [ + "HP:0005321" + ], + "treacher collins syndrome": [ + "HP:0005321" + ], + "prominent nasal septum": [ + "HP:0005322" + ], + "low hang nasal septum": [ + "HP:0005322" + ], + "low hanging nasal septum": [ + "HP:0005322" + ], + "low hang septum of nose": [ + "HP:0005322" + ], + "low hanging septum of nose": [ + "HP:0005322" + ], + "prominent septum of nose": [ + "HP:0005322" + ], + "visible nasal septum": [ + "HP:0005322" + ], + "visible septum of nose": [ + "HP:0005322" + ], + "hemifacial hypertrophy": [ + "HP:0005323" + ], + "enlargement of half of face": [ + "HP:0005323" + ], + "facial hemihyperplasia": [ + "HP:0005323" + ], + "facial hemihypertophy": [ + "HP:0005323" + ], + "friedreich 's disease": [ + "HP:0005323" + ], + "hemifacial enlargement": [ + "HP:0005323" + ], + "hypertrophy of half of face": [ + "HP:0005323" + ], + "increase in size of half of face": [ + "HP:0005323" + ], + "overgrowth of half of face": [ + "HP:0005323" + ], + "disturbance of facial expression": [ + "HP:0005324" + ], + "extension of hair growth on temple to lateral eyebrow": [ + "HP:0005325" + ], + "extension of hair growth on temples to lateral eyebrow": [ + "HP:0005325" + ], + "unusual hairline with hair growth on temple extend to lateral eyebrow": [ + "HP:0005325" + ], + "unusual hairline with hair growth on temples extending to lateral eyebrow": [ + "HP:0005325" + ], + "hypoplastic philtrum": [ + "HP:0005326" + ], + "small philtrum": [ + "HP:0005326" + ], + "loss of facial expression": [ + "HP:0005327" + ], + "progeroid facial appearance": [ + "HP:0005328" + ], + "age facial appearance": [ + "HP:0005328" + ], + "aged facial appearance": [ + "HP:0005328" + ], + "premature age appearance": [ + "HP:0005328" + ], + "premature aged appearance": [ + "HP:0005328" + ], + "prematurely age face": [ + "HP:0005328" + ], + "prematurely aged face": [ + "HP:0005328" + ], + "prematurely age facial appearance": [ + "HP:0005328" + ], + "prematurely aged facial appearance": [ + "HP:0005328" + ], + "wizened face": [ + "HP:0005328" + ], + "fix facial expression": [ + "HP:0005329" + ], + "fixed facial expression": [ + "HP:0005329" + ], + "unchanging facial expression": [ + "HP:0005329" + ], + "recurrent mandibular subluxation": [ + "HP:0005332" + ], + "recurrent mandibular subluxations": [ + "HP:0005332" + ], + "sleepy facial expression": [ + "HP:0005335" + ], + "somnolent facial expression": [ + "HP:0005335" + ], + "forehead hyperpigmentation": [ + "HP:0005336" + ], + "darkening of the forehead": [ + "HP:0005336" + ], + "sparse lateral eyebrow": [ + "HP:0005338" + ], + "lateral hypoplasia of eyebrow": [ + "HP:0005338" + ], + "lateral hypoplasia of eyebrows": [ + "HP:0005338" + ], + "lateral thinning of eyebrow": [ + "HP:0005338" + ], + "lateral thinning of eyebrows": [ + "HP:0005338" + ], + "laterally sparse eyebrow": [ + "HP:0005338" + ], + "laterally sparse eyebrows": [ + "HP:0005338" + ], + "limited hair on end of eyebrow": [ + "HP:0005338" + ], + "sparse lateral eyebrows": [ + "HP:0005338" + ], + "abnormality of complement system": [ + "HP:0005339" + ], + "spastic / hyperactive bladder": [ + "HP:0005340" + ], + "autonomic bladder dysfunction": [ + "HP:0005341" + ], + "hypoplasia of the bladder": [ + "HP:0005343" + ], + "hypoplastic bladder": [ + "HP:0005343" + ], + "underdeveloped bladder": [ + "HP:0005343" + ], + "abnormal carotid artery morphology": [ + "HP:0005344" + ], + "abnormality of the carotid artery": [ + "HP:0005344" + ], + "abnormality of the carotid arteries": [ + "HP:0005344" + ], + "abnormal vena cava morphology": [ + "HP:0005345" + ], + "abnormality of the vena cava": [ + "HP:0005345" + ], + "abnormal facial expression": [ + "HP:0005346" + ], + "cartilaginous trachea": [ + "HP:0005347" + ], + "inspiratory stridor": [ + "HP:0005348" + ], + "hypoplasia of the epiglottis": [ + "HP:0005349" + ], + "hypoplastic epiglottis": [ + "HP:0005349" + ], + "severe t - cell immunodeficiency": [ + "HP:0005352" + ], + "recurrent herpes": [ + "HP:0005353" + ], + "susceptibility to herpesvirus": [ + "HP:0005353" + ], + "lack of t cell function": [ + "HP:0005354" + ], + "absent cellular immunity": [ + "HP:0005354" + ], + "decrease serum complement factor i": [ + "HP:0005356" + ], + "decreased serum complement factor i": [ + "HP:0005356" + ], + "defective b cell differentiation": [ + "HP:0005357" + ], + "aplasia of the thymus": [ + "HP:0005359" + ], + "absent thymic shadow": [ + "HP:0005359" + ], + "absent thymus": [ + "HP:0005359" + ], + "athymia": [ + "HP:0005359" + ], + "lack of thymic shadow": [ + "HP:0005359" + ], + "susceptibility to chickenpox": [ + "HP:0005360" + ], + "humoral immunodeficiency": [ + "HP:0005363" + ], + "obsolete severe viral infection": [ + "HP:0005364" + ], + "obsolete severe viral infections": [ + "HP:0005364" + ], + "severe b lymphocytopenia": [ + "HP:0005365" + ], + "absence of b cell": [ + "HP:0005365" + ], + "absence of b cells": [ + "HP:0005365" + ], + "absent b cell": [ + "HP:0005365" + ], + "absent b cells": [ + "HP:0005365" + ], + "recurrent streptococcus pneumoniae infection": [ + "HP:0005366" + ], + "recurrent streptococcus pneumoniae infections": [ + "HP:0005366" + ], + "abnormality of humoral immunity": [ + "HP:0005368" + ], + "defective humoral immunity": [ + "HP:0005368" + ], + "decrease serum complement factor h": [ + "HP:0005369" + ], + "decreased serum complement factor h": [ + "HP:0005369" + ], + "abnormality of b cell physiology": [ + "HP:0005372" + ], + "reduce b cell function": [ + "HP:0005372" + ], + "reduced b cell function": [ + "HP:0005372" + ], + "cellular immunodeficiency": [ + "HP:0005374" + ], + "obsolete partial cellular immunodeficiency": [ + "HP:0005375" + ], + "recurrent haemophilus influenzae infection": [ + "HP:0005376" + ], + "recurrent haemophilus influenzae infections": [ + "HP:0005376" + ], + "recurrent h. influenzae infection": [ + "HP:0005376" + ], + "recurrent h. influenzae infections": [ + "HP:0005376" + ], + "obsolete severe t lymphocytopenia": [ + "HP:0005379" + ], + "recurrent meningococcal disease": [ + "HP:0005381" + ], + "increase susceptibility to neisseria meningitidis infection": [ + "HP:0005381" + ], + "increased susceptibility to neisseria meningitidis infections": [ + "HP:0005381" + ], + "defective b cell activation": [ + "HP:0005384" + ], + "recurrent protozoan infection": [ + "HP:0005386" + ], + "recurrent protozoan infections": [ + "HP:0005386" + ], + "combine immunodeficiency": [ + "HP:0005387" + ], + "combined immunodeficiency": [ + "HP:0005387" + ], + "depletion of component of the alternative complement pathway": [ + "HP:0005389" + ], + "depletion of components of the alternative complement pathway": [ + "HP:0005389" + ], + "recurrent opportunistic infection": [ + "HP:0005390" + ], + "recurrent opportunistic infections": [ + "HP:0005390" + ], + "frequent opportunistic infection": [ + "HP:0005390" + ], + "frequent opportunistic infections": [ + "HP:0005390" + ], + "susceptibility to coronavirus 229e": [ + "HP:0005396" + ], + "obsolete exaggerated cellular immune process": [ + "HP:0005397" + ], + "obsolete exaggerated cellular immune processes": [ + "HP:0005397" + ], + "reduction of neutrophil motility": [ + "HP:0005400" + ], + "recurrent candida infection": [ + "HP:0005401" + ], + "recurrent candida infections": [ + "HP:0005401" + ], + "frequent candida infection": [ + "HP:0005401" + ], + "frequent candida infections": [ + "HP:0005401" + ], + "obsolete primary t - lymphocyte immune abnormality": [ + "HP:0005402" + ], + "obsolete primary t - lymphocyte immune abnormalities": [ + "HP:0005402" + ], + "t lymphocytopenia": [ + "HP:0005403" + ], + "decrease in t cell count": [ + "HP:0005403" + ], + "decrease in t cell number": [ + "HP:0005403" + ], + "decreased number of circulate t cell": [ + "HP:0005403" + ], + "decreased numbers of circulating t cells": [ + "HP:0005403" + ], + "low t cell count": [ + "HP:0005403" + ], + "reduced number of t cell": [ + "HP:0005403" + ], + "reduced number of t cells": [ + "HP:0005403" + ], + "increase b cell count": [ + "HP:0005404" + ], + "increased b cell count": [ + "HP:0005404" + ], + "increase in b cell count": [ + "HP:0005404" + ], + "increase in b cell number": [ + "HP:0005404" + ], + "increased number of b cell": [ + "HP:0005404" + ], + "increased number of b cells": [ + "HP:0005404" + ], + "recurrent bacterial skin infection": [ + "HP:0005406" + ], + "recurrent bacterial skin infections": [ + "HP:0005406" + ], + "recurrent cutaneous pyogenic infection": [ + "HP:0005406" + ], + "recurrent cutaneous pyogenic infections": [ + "HP:0005406" + ], + "recurrent episode of impetigo": [ + "HP:0005406" + ], + "recurrent episodes of impetigo": [ + "HP:0005406" + ], + "recurrent episode of infectious dermatitis": [ + "HP:0005406" + ], + "recurrent episodes of infectious dermatitis": [ + "HP:0005406" + ], + "recurrent pyogenic skin infection": [ + "HP:0005406" + ], + "recurrent pyogenic skin infections": [ + "HP:0005406" + ], + "decreased proportion of cd4 - positive helper t cell": [ + "HP:0005407" + ], + "decreased proportion of cd4 - positive helper t cells": [ + "HP:0005407" + ], + "abnormality of cd4+ t cell": [ + "HP:0005407" + ], + "abnormality of cd4+ t cells": [ + "HP:0005407" + ], + "cd4 t cell lymphopenia": [ + "HP:0005407" + ], + "cd4+ t - cell lymphopenia": [ + "HP:0005407" + ], + "obsolete markedly reduce t cell function": [ + "HP:0005409" + ], + "obsolete markedly reduced t cell function": [ + "HP:0005409" + ], + "chronic intestinal candidiasis": [ + "HP:0005411" + ], + "candida overgrowth syndrome": [ + "HP:0005411" + ], + "increase alpha - globulin": [ + "HP:0005413" + ], + "increased alpha - globulin": [ + "HP:0005413" + ], + "decreased proportion of cd8 - positive t cell": [ + "HP:0005415" + ], + "decreased proportion of cd8 - positive t cells": [ + "HP:0005415" + ], + "cd8+ t - cell lymphopenia": [ + "HP:0005415" + ], + "decreased proportion of cd8+ t cell": [ + "HP:0005415" + ], + "decreased proportion of cd8+ t cells": [ + "HP:0005415" + ], + "decreased proportion of cd8 - positive , alpha - beta t cell": [ + "HP:0005415" + ], + "decreased proportion of cd8 - positive , alpha - beta t cells": [ + "HP:0005415" + ], + "decrease serum complement factor b": [ + "HP:0005416" + ], + "decreased serum complement factor b": [ + "HP:0005416" + ], + "decrease serum factor b": [ + "HP:0005416" + ], + "decreased serum factor b": [ + "HP:0005416" + ], + "decrease t cell activation": [ + "HP:0005419" + ], + "decreased t cell activation": [ + "HP:0005419" + ], + "decrease t lymphocyte activation": [ + "HP:0005419" + ], + "decreased t lymphocyte activation": [ + "HP:0005419" + ], + "decrease t - cell activation": [ + "HP:0005419" + ], + "decreased t - cell activation": [ + "HP:0005419" + ], + "decrease t - lymphocyte activation": [ + "HP:0005419" + ], + "decreased t - lymphocyte activation": [ + "HP:0005419" + ], + "defective t cell activation": [ + "HP:0005419" + ], + "profound depletion of t4+ lymphocyte": [ + "HP:0005419" + ], + "profound depletion of t4+ lymphocytes": [ + "HP:0005419" + ], + "recurrent gram - negative bacterial infection": [ + "HP:0005420" + ], + "recurrent gram - negative bacterial infections": [ + "HP:0005420" + ], + "decrease serum complement c3": [ + "HP:0005421" + ], + "decreased serum complement c3": [ + "HP:0005421" + ], + "decrease serum c3": [ + "HP:0005421" + ], + "decreased serum c3": [ + "HP:0005421" + ], + "decrease serum complement c3 level": [ + "HP:0005421" + ], + "decreased serum complement c3 level": [ + "HP:0005421" + ], + "absence of cd8 - positive t cell": [ + "HP:0005422" + ], + "absence of cd8 - positive t cells": [ + "HP:0005422" + ], + "absence of cd8+ t cell": [ + "HP:0005422" + ], + "absence of cd8+ t cells": [ + "HP:0005422" + ], + "dysfunctional alternative complement pathway": [ + "HP:0005423" + ], + "absent specific antibody response": [ + "HP:0005424" + ], + "recurrent sinopulmonary infection": [ + "HP:0005425" + ], + "recurrent sinopulmonary infections": [ + "HP:0005425" + ], + "chronic sinopulmonary infection": [ + "HP:0005425" + ], + "recurrent sinus and lung infection": [ + "HP:0005425" + ], + "recurrent sinus and lung infections": [ + "HP:0005425" + ], + "severe recurrent varicella": [ + "HP:0005428" + ], + "recurrent systemic pyogenic infection": [ + "HP:0005429" + ], + "recurrent systemic pyogenic infections": [ + "HP:0005429" + ], + "recurrent neisserial infection": [ + "HP:0005430" + ], + "recurrent neisserial infections": [ + "HP:0005430" + ], + "episode of neisserial infection": [ + "HP:0005430" + ], + "episodes of neisserial infection": [ 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[ + "HP:0005439" + ], + "sclerotic cranial suture": [ + "HP:0005441" + ], + "sclerotic cranial sutures": [ + "HP:0005441" + ], + "widely patent coronal suture": [ + "HP:0005442" + ], + "enlarge posterior fossa": [ + "HP:0005445" + ], + "enlarged posterior fossa": [ + "HP:0005445" + ], + "widen posterior fossa": [ + "HP:0005445" + ], + "widened posterior fossa": [ + "HP:0005445" + ], + "obtuse angle of mandible": [ + "HP:0005446" + ], + "high mandibular plane angle": [ + "HP:0005446" + ], + "steep mandibular plane angle": [ + "HP:0005446" + ], + "bridge sella turcica": [ + "HP:0005449" + ], + "bridged sella turcica": [ + "HP:0005449" + ], + "calvarial osteosclerosis": [ + "HP:0005450" + ], + "decrease cranial base ossification": [ + "HP:0005451" + ], + "decreased cranial base ossification": [ + "HP:0005451" + ], + "absent / hypoplastic paranasal sinus": [ + "HP:0005453" + ], + "absent / hypoplastic paranasal sinuses": [ + "HP:0005453" + ], + "absent ethmoidal sinus": [ + "HP:0005456" + ], + "absent ethmoidal sinuses": [ + "HP:0005456" + ], + "agenesis of ethmoid sinus": [ + "HP:0005456" + ], + "agenesis of ethmoid sinuses": [ + "HP:0005456" + ], + "failure of development of ethmoid sinus": [ + "HP:0005456" + ], + "failure of development of ethmoid sinuses": [ + "HP:0005456" + ], + "miss ethmoid sinus": [ + "HP:0005456" + ], + "missing ethmoid sinuses": [ + "HP:0005456" + ], + "premature closure of fontanelle": [ + "HP:0005458" + ], + "premature closure of fontanelles": [ + "HP:0005458" + ], + "early closure of the bregma suture": [ + "HP:0005458" + ], + "early closure of the bregma sutures": [ + "HP:0005458" + ], + "early closure of the cranial suture": [ + "HP:0005458" + ], + "early closure of the cranial sutures": [ + "HP:0005458" + ], + "early closure of the fontanelle": [ + "HP:0005458" + ], + "early closure of the fontanelles": [ + "HP:0005458" + ], + "obliterate fontanelle": [ + "HP:0005458" + ], + "obliterated fontanelles": [ + "HP:0005458" + ], + "premature closure of the bregma suture": [ + "HP:0005458" + ], + "premature closure of the bregma sutures": [ + "HP:0005458" + ], + "premature closure of the cranial suture": [ + "HP:0005458" + ], + "premature closure of the cranial sutures": [ + "HP:0005458" + ], + "craniofacial disproportion": [ + "HP:0005461" + ], + "calcification of falx cerebri": [ + "HP:0005462" + ], + "elongate sella turcica": [ + "HP:0005463" + ], + "elongated sella turcica": [ + "HP:0005463" + ], + "craniofacial osteosclerosis": [ + "HP:0005464" + ], + "cranial sclerosis": [ + "HP:0005464" + ], + "facial hyperostosis": [ + "HP:0005465" + ], + "enlargement of facial bone": [ + "HP:0005465" + ], + "enlargement of facial bones": [ + "HP:0005465" + ], + "enlargement of facial skeleton": [ + "HP:0005465" + ], + "enlargment of the facial bone": [ + "HP:0005465" + ], + "enlargment of the facial bones": [ + "HP:0005465" + ], + "excessive growth of facial bone": [ + "HP:0005465" + ], + "excessive growth of facial bones": [ + "HP:0005465" + ], + "excessive growth of facial skeleton": [ + "HP:0005465" + ], + "hyperostosis of facial bone": [ + "HP:0005465" + ], + "hyperostosis of facial bones": [ + "HP:0005465" + ], + "hyperostosis of facial skeleton": [ + "HP:0005465" + ], + "hypertrophy of facial bone": [ + "HP:0005465" + ], + "hypertrophy of facial bones": [ + "HP:0005465" + ], + "hypertrophy of facial skeleton": [ + "HP:0005465" + ], + "hypertrophy of the facial bone": [ + "HP:0005465" + ], + "hypertrophy of the facial bones": [ + "HP:0005465" + ], + "increase in size of the facial bone": [ + "HP:0005465" + ], + "increase in size of the facial bones": [ + "HP:0005465" + ], + "increase ossification of facial bone": [ + "HP:0005465" + ], + "increased ossification of facial bones": [ + "HP:0005465" + ], + "increase ossification of facial skeleton": [ + "HP:0005465" + ], + "increased ossification of facial skeleton": [ + "HP:0005465" + ], + "overgrowth of facial bone": [ + "HP:0005465" + ], + "overgrowth of facial bones": [ + "HP:0005465" + ], + "overgrowth of facial skeleton": [ + "HP:0005465" + ], + "overgrowth of the facial bone": [ + "HP:0005465" + ], + "overgrowth of the facial bones": [ + "HP:0005465" + ], + "hypoplasia of the frontal bone": [ + "HP:0005466" + ], + "decreased size of bone of forehead": [ + "HP:0005466" + ], + "hypoplastic frontal bone": [ + "HP:0005466" + ], + "hypoplastic frontal bones": [ + "HP:0005466" + ], + "hypotrophic frontal bone": [ + "HP:0005466" + ], + "hypotrophic frontal bones": [ + "HP:0005466" + ], + "small bone of forehead": [ + "HP:0005466" + ], + "thin bone of forehead": [ + "HP:0005466" + ], + "underdevelopment of bone of forehead": [ + "HP:0005466" + ], + "flat occiput": [ + "HP:0005469" + ], + "flat back of skull": [ + "HP:0005469" + ], + "flat back of the head": [ + "HP:0005469" + ], + "flat back of the skull": [ + "HP:0005469" + ], + "flat posterior cranium": [ + "HP:0005469" + ], + "flat posterior head": [ + "HP:0005469" + ], + "posterior flattening of the skull": [ + "HP:0005469" + ], + "orbital craniosynostosis": [ + "HP:0005472" + ], + "fusion of middle ear ossicle": [ + "HP:0005473" + ], + "fusion of middle ear ossicles": [ + "HP:0005473" + ], + "decrease calvarial ossification": [ + "HP:0005474" + ], + "decreased calvarial ossification": [ + "HP:0005474" + ], + "poorly ossify calvaria": [ + "HP:0005474" + ], + "poorly ossified calvaria": [ + "HP:0005474" + ], + "poorly ossify calvarium": [ + "HP:0005474" + ], + "poorly ossified calvarium": [ + "HP:0005474" + ], + "skull soft on palpation": [ + "HP:0005474" + ], + "soft calvaria": [ + "HP:0005474" + ], + "soft skullcap": [ + "HP:0005474" + ], + "undermineralized calvarium": [ + "HP:0005474" + ], + "widely patent sagittal suture": [ + "HP:0005476" + ], + "progressive sclerosis of skull base": [ + "HP:0005477" + ], + "prominent frontal sinus": [ + "HP:0005478" + ], + "prominent frontal sinuses": [ + "HP:0005478" + ], + "hyperplasia of frontal sinus": [ + "HP:0005478" + ], + "hypertrophy of frontal sinus": [ + "HP:0005478" + ], + "increase size of frontal sinus": [ + "HP:0005478" + ], + "increased size of frontal sinus": [ + "HP:0005478" + ], + "increased volume of frontal sinus": [ + "HP:0005478" + ], + "large frontal sinus": [ + "HP:0005478" + ], + "decrease circulating ige": [ + "HP:0005479" + ], + "decreased circulating ige": [ + "HP:0005479" + ], + "decrease ige": [ + "HP:0005479" + ], + "decreased ige": [ + "HP:0005479" + ], + "ige deficiency": [ + "HP:0005479" + ], + "abnormality of the alternative complement pathway": [ + "HP:0005482" + ], + "abnormal epiglottis morphology": [ + "HP:0005483" + ], + "abnormality of the epiglottis": [ + "HP:0005483" + ], + "secondary microcephaly": [ + "HP:0005484" + ], + "acquire microcephaly": [ + "HP:0005484" + ], + "acquired microcephaly": [ + "HP:0005484" + ], + "deceleration of head growth": [ + "HP:0005484" + ], + "development of small head that be not present at birth": [ + "HP:0005484" + ], + "development of small head that was not present at birth": [ + "HP:0005484" + ], + "microcephaly , acquire": [ + "HP:0005484" + ], + "microcephaly , acquired": [ + "HP:0005484" + ], + "microcephaly , postnatal": [ + "HP:0005484" + ], + "postnatal deceleration of head circumference": [ + "HP:0005484" + ], + "postnatal microcephaly": [ + "HP:0005484" + ], + "small fontanelle": [ + "HP:0005486" + ], + "little cranial suture": [ + "HP:0005486" + ], + "little cranial sutures": [ + "HP:0005486" + ], + "little fontanelle": [ + "HP:0005486" + ], + "microfontanelle": [ + "HP:0005486" + ], + "small bregma suture": [ + "HP:0005486" + ], + "small bregma sutures": [ + "HP:0005486" + ], + "small cranial suture": [ + "HP:0005486" + ], + "small cranial sutures": [ + "HP:0005486" + ], + "small soft spot": [ + "HP:0005486" + ], + "prominent metopic ridge": [ + "HP:0005487" + ], + "prominent frontal ridge": [ + "HP:0005487" + ], + "prominent frontal suture": [ + "HP:0005487" + ], + "prominent metopic suture": [ + "HP:0005487" + ], + "ridging of frontal suture": [ + "HP:0005487" + ], + "ridging of metopic suture": [ + "HP:0005487" + ], + "postnatal macrocephaly": [ + "HP:0005490" + ], + "macrocephaly , postnatal": [ + "HP:0005490" + ], + "premature posterior fontanelle closure": [ + "HP:0005494" + ], + "metopic suture patent to nasal root": [ + "HP:0005495" + ], + "midline skin dimple over anterior / posterior fontanelle": [ + "HP:0005498" + ], + "midline skin dimples over anterior / posterior fontanelles": [ + "HP:0005498" + ], + "increase red cell osmotic fragility": [ + "HP:0005502" + ], + "increased red cell osmotic fragility": [ + "HP:0005502" + ], + "increase erythrocyte osmotic fragility": [ + "HP:0005502" + ], + "increased erythrocyte osmotic fragility": [ + "HP:0005502" + ], + "increase red cell fragility": [ + "HP:0005502" + ], + "increased red cell fragility": [ + "HP:0005502" + ], + "refractory anemia": [ + "HP:0005505" + ], + "refractory anaemia": [ + "HP:0005505" + ], + "chronic myelogenous leukemia": [ + "HP:0005506" + ], + "chronic myelocytic leukaemia": [ + "HP:0005506" + ], + "chronic myelocytic leukemia": [ + "HP:0005506" + ], + "chronic myelogenous leukaemia": [ + "HP:0005506" + ], + "chronic myeloid leukaemia": [ + "HP:0005506" + ], + "chronic myeloid leukemia": [ + "HP:0005506" + ], + "hemoglobin bart": [ + "HP:0005507" + ], + "hemoglobin barts": [ + "HP:0005507" + ], + "haemoglobin bart": [ + "HP:0005507" + ], + "haemoglobin barts": [ + "HP:0005507" + ], + "hb bart": [ + "HP:0005507" + ], + "hb barts": [ + "HP:0005507" + ], + "monoclonal immunoglobulin m proteinemia": [ + "HP:0005508" + ], + "waldenstrom macroglobulinemia": [ + "HP:0005508" + ], + "transient erythroblastopenia": [ + "HP:0005510" + ], + "transient decrease in blood erythrocyte number": [ + "HP:0005510" + ], + "heinz body anemia": [ + "HP:0005511" + ], + "heinz body anaemia": [ + "HP:0005511" + ], + "impaired neutrophil killing of staphylococci": [ + "HP:0005512" + ], + "increase megakaryocyte count": [ + "HP:0005513" + ], + "increased megakaryocyte count": [ + "HP:0005513" + ], + "t - cell lymphoma / leukemia": [ + "HP:0005517" + ], + "increase mean corpuscular volume": [ + "HP:0005518" + ], + "increased mean corpuscular volume": [ + "HP:0005518" + ], + "erythrocyte macrocytosis": [ + "HP:0005518" + ], + "increase mcv": [ + "HP:0005518" + ], + "increased mcv": [ + "HP:0005518" + ], + "chronic disseminate intravascular coagulation": [ + "HP:0005520" + ], + "chronic disseminated intravascular coagulation": [ + "HP:0005520" + ], + "chronic consumption coagulopathy": [ + "HP:0005520" + ], + "compensate disseminate intravascular coagulation": [ + "HP:0005520" + ], + "compensated disseminated intravascular coagulation": [ + "HP:0005520" + ], + "disseminate intravascular coagulation": [ + "HP:0005521" + ], + "disseminated intravascular coagulation": [ + "HP:0005521" + ], + "pyridoxine - responsive sideroblastic anemia": [ + "HP:0005522" + ], + "pyridoxine - responsive sideroblastic anaemia": [ + "HP:0005522" + ], + "lymphoproliferative disorder": [ + "HP:0005523" + ], + "lymphoproliferative disorders": [ + "HP:0005523" + ], + "macrocytic hemolytic disease": [ + "HP:0005524" + ], + "spontaneous hemolytic crisis": [ + "HP:0005525" + ], + "spontaneous hemolytic crises": [ + "HP:0005525" + ], + "lymphoid leukemia": [ + "HP:0005526" + ], + "lymphoid leukaemia": [ + "HP:0005526" + ], + "reduce kininogen activity": [ + "HP:0005527" + ], + "reduced kininogen activity": [ + "HP:0005527" + ], + "fitzgerald factor deficiency": [ + "HP:0005527" + ], + "kininogen deficiency": [ + "HP:0005527" + ], + "williams factor deficiency": [ + "HP:0005527" + ], + "williams - fitzgerald - flaujeac factor deficiency": [ + "HP:0005527" + ], + "bone marrow hypocellularity": [ + "HP:0005528" + ], + "bone marrow failure": [ + "HP:0005528" + ], + "bone marrow hypoplasia": [ + "HP:0005528" + ], + "hypoplastic bone marrow": [ + "HP:0005528" + ], + "biphenotypic acute leukemia": [ + "HP:0005531" + ], + "acute biphenotypic leukaemia": [ + "HP:0005531" + ], + "biphenotypic acute leukaemia": [ + "HP:0005531" + ], + "myeloid / lymphoid leukaemia": [ + "HP:0005531" + ], + "myeloid / lymphoid leukemia": [ + "HP:0005531" + ], + "macrocytic dyserythropoietic anemia": [ + "HP:0005532" + ], + "macrocytic dyserythropoietic anaemia": [ + "HP:0005532" + ], + "transient myeloproliferative syndrome": [ + "HP:0005534" + ], + "transient leukaemia of down syndrome": [ + "HP:0005534" + ], + "transient leukemia of down syndrome": [ + "HP:0005534" + ], + "transient myeloproliferative disorder": [ + "HP:0005534" + ], + "exercise - induced hemolysis": [ + "HP:0005535" + ], + "decrease mean platelet volume": [ + "HP:0005537" + ], + "decreased mean platelet volume": [ + "HP:0005537" + ], + "small platelet size": [ + "HP:0005537" + ], + "small platelet": [ + "HP:0005537" + ], + "small platelets": [ + "HP:0005537" + ], + "small platelets size": [ + "HP:0005537" + ], + "t cell chronic lymphocytic lymphoma / leukemia": [ + "HP:0005539" + ], + "red blood cell keratocytosis": [ + "HP:0005540" + ], + "distort red blood cell resemble keratocytes": [ + "HP:0005540" + ], + "distorted red blood cells resembling keratocytes": [ + "HP:0005540" + ], + "rbc keratocytosis": [ + "HP:0005540" + ], + "congenital agranulocytosis": [ + "HP:0005541" + ], + "prolonged whole - blood clotting time": [ + "HP:0005542" + ], + "prolong clotting time": [ + "HP:0005542" + ], + "prolonged clotting time": [ + "HP:0005542" + ], + "reduce protein c activity": [ + "HP:0005543" + ], + "reduced protein c activity": [ + "HP:0005543" + ], + "protein c deficiency": [ + "HP:0005543" + ], + "increase red cell osmotic resistance": [ + "HP:0005546" + ], + "increased red cell osmotic resistance": [ + "HP:0005546" + ], + "myeloproliferative disorder": [ + "HP:0005547" + ], + "megakaryocytopenia": [ + "HP:0005548" + ], + "obsolete congenital neutropenia": [ + "HP:0005549" + ], + "chronic lymphatic leukemia": [ + "HP:0005550" + ], + "chronic lymphatic leukaemia": [ + "HP:0005550" + ], + "chronic lymphocytic leukaemia": [ + "HP:0005550" + ], + "chronic lymphocytic leukemia": [ + "HP:0005550" + ], + "abnormality of the metopic suture": [ + "HP:0005556" + ], + "abnormality of the zygomatic arch": [ + "HP:0005557" + ], + "abnormality of the malar arch": [ + "HP:0005557" + ], + "anomaly of the malar arch": [ + "HP:0005557" + ], + "anomaly of the zygomatic arch": [ + "HP:0005557" + ], + "deformity of the malar arch": [ + "HP:0005557" + ], + "deformity of the zygomatic arch": [ + "HP:0005557" + ], + "malformation of the malar arch": [ + "HP:0005557" + ], + "malformation of the zygomatic arch": [ + "HP:0005557" + ], + "chronic leukemia": [ + "HP:0005558" + ], + "chronic blood cancer": [ + "HP:0005558" + ], + "chronic leukaemia": [ + "HP:0005558" + ], + "abnormality of the kinin - kallikrein system": [ + "HP:0005559" + ], + "imbalanced hemoglobin synthesis": [ + "HP:0005560" + ], + "imbalanced haemoglobin synthesis": [ + "HP:0005560" + ], + "imbalanced hb synthesis": [ + "HP:0005560" + ], + "abnormality of bone marrow cell morphology": [ + "HP:0005561" + ], + "anomaly of the bone marrow cell": [ + "HP:0005561" + ], + "anomaly of the bone marrow cells": [ + "HP:0005561" + ], + "bone marrow disease": [ + "HP:0005561" + ], + "multiple renal cyst": [ + "HP:0005562" + ], + "multiple renal cysts": [ + "HP:0005562" + ], + "multiple kidney cyst": [ + "HP:0005562" + ], + "multiple kidney cysts": [ + "HP:0005562" + ], + "decreased number of nephron": [ + "HP:0005563" + ], + "decreased numbers of nephrons": [ + "HP:0005563" + ], + "decreased number of glomerulus": [ + "HP:0005563" + ], + "decreased numbers of glomeruli": [ + "HP:0005563" + ], + "oligonephronia": [ + "HP:0005563" + ], + "absence of renal corticomedullary differentiation": [ + "HP:0005564" + ], + "absent renal corticomedullary differentiation": [ + "HP:0005564" + ], + "loss of corticomedullary differentiation": [ + "HP:0005564" + ], + "reduce renal corticomedullary differentiation": [ + "HP:0005565" + ], + "reduced renal corticomedullary differentiation": [ + "HP:0005565" + ], + "loss of definition of corticomedullary differentiation": [ + "HP:0005565" + ], + "renal magnesium wasting": [ + "HP:0005567" + ], + "increase renal tubular phosphate reabsorption": [ + "HP:0005571" + ], + "increased renal tubular phosphate reabsorption": [ + "HP:0005571" + ], + "increase percent tubular reabsorption of phosphorus": [ + "HP:0005571" + ], + "increased percent tubular reabsorption of phosphorus": [ + "HP:0005571" + ], + "decrease renal tubular phosphate excretion": [ + "HP:0005572" + ], + "decreased renal tubular phosphate excretion": [ + "HP:0005572" + ], + "non - acidotic proximal tubulopathy": [ + "HP:0005574" + ], + "hemolytic - uremic syndrome": [ + "HP:0005575" + ], + "hemolytic uremic syndrome": [ + "HP:0005575" + ], + "tubulointerstitial fibrosis": [ + "HP:0005576" + ], + "tubulointerstitial renal fibrosis": [ + "HP:0005576" + ], + "tubulointerstitial scarring": [ + "HP:0005576" + ], + "impaired reabsorption of chloride": [ + "HP:0005579" + ], + "impaired reabsorption of cl": [ + "HP:0005579" + ], + "impaired reabsorption of cl -": [ + "HP:0005579" + ], + "duplication of renal pelvis": [ + "HP:0005580" + ], + "tubular basement membrane disintegration": [ + "HP:0005583" + ], + "disintegration of the tubular basement membrane": [ + "HP:0005583" + ], + "renal cell carcinoma": [ + "HP:0005584" + ], + "cancer start in small tube in kidney": [ + "HP:0005584" + ], + "cancer starting in small tubes in kidneys": [ + "HP:0005584" + ], + "hypernephroma": [ + "HP:0005584" + ], + "renal carcinoma": [ + "HP:0005584" + ], + "spotty hyperpigmentation": [ + "HP:0005585" + ], + "patchy hyperpigmentation": [ + "HP:0005585" + ], + "spotty increase pigmentation": [ + "HP:0005585" + ], + "spotty increased pigmentation": [ + "HP:0005585" + ], + "hyperpigmentation in sun - expose area": [ + "HP:0005586" + ], + "hyperpigmentation in sun - exposed areas": [ + "HP:0005586" + ], + "hyperpigmentation of expose area": [ + "HP:0005586" + ], + "hyperpigmentation of exposed areas": [ + "HP:0005586" + ], + "increase pigmentation in sun - expose area": [ + "HP:0005586" + ], + "increased pigmentation in sun - exposed areas": [ + "HP:0005586" + ], + "profuse pigment skin lesion": [ + "HP:0005587" + ], + "profuse pigmented skin lesions": [ + "HP:0005587" + ], + "patchy palmoplantar hyperkeratosis": [ + "HP:0005588" + ], + "palmoplantar keratoderma , patchy": [ + "HP:0005588" + ], + "patchy palmoplantar keratoderma": [ + "HP:0005588" + ], + "spotty hypopigmentation": [ + "HP:0005590" + ], + "patchy depigmentation": [ + "HP:0005590" + ], + "patchy hypopigmentation": [ + "HP:0005590" + ], + "spotty decrease pigmentation": [ + "HP:0005590" + ], + "spotty decreased pigmentation": [ + "HP:0005590" + ], + "giant melanosomes in melanocyte": [ + "HP:0005592" + ], + "giant melanosomes in melanocytes": [ + "HP:0005592" + ], + "macromelanosomes": [ + "HP:0005592" + ], + "macular hypopigmented whorl , streak , and patch": [ + "HP:0005593" + ], + "macular hypopigmented whorls , streaks , and patches": [ + "HP:0005593" + ], + "generalize hyperkeratosis": [ + "HP:0005595" + ], + "generalized hyperkeratosis": [ + "HP:0005595" + ], + "generalise hyperkeratosis": [ + "HP:0005595" + ], + "generalised hyperkeratosis": [ + "HP:0005595" + ], + "hyperkeratosis , generalise": [ + "HP:0005595" + ], + "hyperkeratosis , generalised": [ + "HP:0005595" + ], + "hyperkeratosis , generalize": [ + "HP:0005595" + ], + "hyperkeratosis , generalized": [ + "HP:0005595" + ], + "congenital alopecia totalis": [ + "HP:0005597" + ], + "facial telangiectasia in butterfly midface distribution": [ + "HP:0005598" + ], + "butterfly facial telangiectasia": [ + "HP:0005598" + ], + "hypopigmentation of hair": [ + "HP:0005599" + ], + "hair hypopigmentation": [ + "HP:0005599" + ], + "loss of hair color": [ + "HP:0005599" + ], + "loss of hair colour": [ + "HP:0005599" + ], + "congenital giant melanocytic nevus": [ + "HP:0005600" + ], + "giant pigment hairy nevus": [ + "HP:0005600" + ], + "giant pigmented hairy nevus": [ + "HP:0005600" + ], + "giant pigment mole": [ + "HP:0005600" + ], + "giant pigmented mole": [ + "HP:0005600" + ], + "giant pigment nevus": [ + "HP:0005600" + ], + "giant pigmented nevus": [ + "HP:0005600" + ], + "progressive vitiligo": [ + "HP:0005602" + ], + "numerous congenital melanocytic nevus": [ + "HP:0005603" + ], + "numerous congenital melanocytic nevi": [ + "HP:0005603" + ], + "large cafe - au - lait macule with irregular margin": [ + "HP:0005605" + ], + "large cafe - au - lait macules with irregular margins": [ + "HP:0005605" + ], + "hyperpigmented nevus and streak": [ + "HP:0005606" + ], + "hyperpigmented nevi and streak": [ + "HP:0005606" + ], + "abnormal tracheobronchial morphology": [ + "HP:0005607" + ], + "tracheobronchial anomaly": [ + "HP:0005607" + ], + "tracheobronchial anomalies": [ + "HP:0005607" + ], + "bilobate gallbladder": [ + "HP:0005608" + ], + "bilobed gallbladder": [ + "HP:0005608" + ], + "double gallbladder": [ + "HP:0005608" + ], + "gallbladder duplication": [ + "HP:0005608" + ], + "gallbladder dysfunction": [ + "HP:0005609" + ], + "arthrogryposis - like hand anomaly": [ + "HP:0005612" + ], + "aplasia / hypoplasia of the femur": [ + "HP:0005613" + ], + "absent / small thighbone": [ + "HP:0005613" + ], + "absent / underdevelop thighbone": [ + "HP:0005613" + ], + "absent / underdeveloped thighbone": [ + "HP:0005613" + ], + "hypoplastic to absent femur": [ + "HP:0005613" + ], + "hypoplastic to absent femora": [ + "HP:0005613" + ], + "hypoplastic / aplastic femur": [ + "HP:0005613" + ], + "hypoplastic / aplastic femora": [ + "HP:0005613" + ], + "accelerate skeletal maturation": [ + "HP:0005616" + ], + "accelerated skeletal maturation": [ + "HP:0005616" + ], + "advanced bone age": [ + "HP:0005616" + ], + "early bone maturation": [ + "HP:0005616" + ], + "bilateral camptodactyly": [ + "HP:0005617" + ], + "thoracolumbar kyphosis": [ + "HP:0005619" + ], + "thoracolumbar gibbus": [ + "HP:0005619" + ], + "thoracolumbar gibbus deformity": [ + "HP:0005619" + ], + "hypermobility of interphalangeal joint": [ + "HP:0005620" + ], + "hypermobility of interphalangeal joints": [ + "HP:0005620" + ], + "increase mobility of hinge joint": [ + "HP:0005620" + ], + "increased mobility of hinge joints": [ + "HP:0005620" + ], + "trapezoidal shape vertebral body": [ + "HP:0005621" + ], + "trapezoidal shaped vertebral bodies": [ + "HP:0005621" + ], + "broad long bone": [ + "HP:0005622" + ], + "broad long bones": [ + "HP:0005622" + ], + "wide long bone": [ + "HP:0005622" + ], + "wide long bones": [ + "HP:0005622" + ], + "widen long bone": [ + "HP:0005622" + ], + "widened long bones": [ + "HP:0005622" + ], + "absent ossification of calvaria": [ + "HP:0005623" + ], + "absent bone maturation of skullcap": [ + "HP:0005623" + ], + "absent ossification of skull vault": [ + "HP:0005623" + ], + "osteoporosis of vertebra": [ + "HP:0005625" + ], + "osteoporosis of vertebrae": [ + "HP:0005625" + ], + "posterior fusion of lumbosacral vertebra": [ + "HP:0005626" + ], + "posterior fusion of lumbosacral vertebrae": [ + "HP:0005626" + ], + "type d brachydactyly": [ + "HP:0005627" + ], + "brachydactyly type d": [ + "HP:0005627" + ], + "absent forearm": [ + "HP:0005632" + ], + "absent forearms": [ + "HP:0005632" + ], + "decrease anterioposterior diameter of lumbar vertebral body": [ + "HP:0005638" + ], + "decreased anterioposterior diameter of lumbar vertebral bodies": [ + "HP:0005638" + ], + "hyperextensible hand joint": [ + "HP:0005639" + ], + "hyperextensible hand joints": [ + "HP:0005639" + ], + "abnormal vertebral segmentation and fusion": [ + "HP:0005640" + ], + "short 3rd toe": [ + "HP:0005643" + ], + "brachydactyly of third toe": [ + "HP:0005643" + ], + "brachydactyly of third toes": [ + "HP:0005643" + ], + "short third toe": [ + "HP:0005643" + ], + "intervertebral disk calcification": [ + "HP:0005645" + ], + "intervertebral disc calcification": [ + "HP:0005645" + ], + "multiple intervertebral disc calcification": [ + "HP:0005645" + ], + "multiple intervertebral disc calcifications": [ + "HP:0005645" + ], + "multiple intervertebral disk calcification": [ + "HP:0005645" + ], + "multiple intervertebral disk calcifications": [ + "HP:0005645" + ], + "bilateral ulnar hypoplasia": [ + "HP:0005648" + ], + "cutaneous syndactyly between finger 2 and 5": [ + "HP:0005650" + ], + "cutaneous syndactyly between fingers 2 and 5": [ + "HP:0005650" + ], + "cortical sclerosis": [ + "HP:0005652" + ], + "moderate generalize osteoporosis": [ + "HP:0005653" + ], + "moderate generalized osteoporosis": [ + "HP:0005653" + ], + "moderate generalise osteoporosis": [ + "HP:0005653" + ], + "moderate generalised osteoporosis": [ + "HP:0005653" + ], + "multiple digital exostosis": [ + "HP:0005655" + ], + "multiple digital exostoses": [ + "HP:0005655" + ], + "positional foot deformity": [ + "HP:0005656" + ], + "thoracic kyphoscoliosis": [ + "HP:0005659" + ], + "salmonella osteomyelitis": [ + "HP:0005661" + ], + "salmonella bone infection": [ + "HP:0005661" + ], + "massively thicken long bone cortex": [ + "HP:0005665" + ], + "massively thickened long bone cortices": [ + "HP:0005665" + ], + "o odontoideum": [ + "HP:0005667" + ], + "os odontoideum": [ + "HP:0005667" + ], + "bilateral intracerebral calcification": [ + "HP:0005671" + ], + "bilateral intracerebral calcifications": [ + "HP:0005671" + ], + "bilateral intracranial calcification": [ + "HP:0005671" + ], + "bilateral intracranial calcifications": [ + "HP:0005671" + ], + "rudimentary postaxial polydactyly of hand": [ + "HP:0005676" + ], + "rudimentary postaxial polydactyly of hands": [ + "HP:0005676" + ], + "anterior atlanto - occipital dislocation": [ + "HP:0005678" + ], + "dupuytren contracture": [ + "HP:0005679" + ], + "tongue - like lumbar vertebral deformity": [ + "HP:0005680" + ], + "tongue - like lumbar vertebral deformities": [ + "HP:0005680" + ], + "juvenile rheumatoid arthritis": [ + "HP:0005681" + ], + "juvenile idiopathic arthritis": [ + "HP:0005681" + ], + "juvenile ra": [ + "HP:0005681" + ], + "rheumatoid arthritis , juvenile": [ + "HP:0005681" + ], + "talocalcaneal synostosis": [ + "HP:0005682" + ], + "fusion of foot joint": [ + "HP:0005682" + ], + "fusion of the subtalar joint": [ + "HP:0005682" + ], + "distal arthrogryposis": [ + "HP:0005684" + ], + "patchy osteosclerosis": [ + "HP:0005686" + ], + "patchy increase of bone mineral density": [ + "HP:0005686" + ], + "uneven increase in bone density": [ + "HP:0005686" + ], + "deform humeral head": [ + "HP:0005687" + ], + "deformed humeral heads": [ + "HP:0005687" + ], + "deform head of long bone in upper arm": [ + "HP:0005687" + ], + "deformed head of long bone in upper arm": [ + "HP:0005687" + ], + "dysplastic distal thumb phalanx with a central hole": [ + "HP:0005688" + ], + "dysplastic distal thumb phalanges with a central hole": [ + "HP:0005688" + ], + "dermatoglyphic ridge abnormal": [ + "HP:0005689" + ], + "dermatoglyphic ridges abnormal": [ + "HP:0005689" + ], + "joint hyperflexibility": [ + "HP:0005692" + ], + "joint move beyond expect range of motion": [ + "HP:0005692" + ], + "joints move beyond expected range of motion": [ + "HP:0005692" + ], + "partial fusion of proximal row of carpal bone": [ + "HP:0005694" + ], + "partial fusion of proximal row of carpal bones": [ + "HP:0005694" + ], + "partial fusion of innermost row of wrist bone": [ + "HP:0005694" + ], + "partial fusion of innermost row of wrist bones": [ + "HP:0005694" + ], + "postaxial polydactyly type a": [ + "HP:0005696" + ], + "increase bone density with cystic change": [ + "HP:0005700" + ], + "increased bone density with cystic changes": [ + "HP:0005700" + ], + "multiple enchondromatosis": [ + "HP:0005701" + ], + "bilateral triphalangeal thumb": [ + "HP:0005707" + ], + "bilateral triphalangeal thumbs": [ + "HP:0005707" + ], + "bilateral digitalize thumb": [ + "HP:0005707" + ], + "bilateral digitalized thumb": [ + "HP:0005707" + ], + "2 - 3 toe cutaneous syndactyly": [ + "HP:0005709" + ], + "complete cutaneous syndactyly of second and third toe": [ + "HP:0005709" + ], + "complete cutaneous syndactyly of second and third toes": [ + "HP:0005709" + ], + "cutaneous 2,3 toe syndactyly": [ + "HP:0005709" + ], + "cutaneous syndactyly of second and third toe": [ + "HP:0005709" + ], + "cutaneous syndactyly of second and third toes": [ + "HP:0005709" + ], + "webbed skin of 2nd - 3rd toe": [ + "HP:0005709" + ], + "webbed skin of 2nd - 3rd toes": [ + "HP:0005709" + ], + "flatten knee epiphysis": [ + "HP:0005715" + ], + "flattened knee epiphyses": [ + "HP:0005715" + ], + "flatten end part of knee bone": [ + "HP:0005715" + ], + "flattened end part of knee bone": [ + "HP:0005715" + ], + "lethal skeletal dysplasia": [ + "HP:0005716" + ], + "lethal dwarfism identifiable at birth": [ + "HP:0005716" + ], + "shortening of all metacarpal": [ + "HP:0005720" + ], + "shortening of all metacarpals": [ + "HP:0005720" + ], + "hyperextensible thumb": [ + "HP:0005722" + ], + "double joint thumb": [ + "HP:0005722" + ], + "double jointed thumb": [ + "HP:0005722" + ], + "shoe - shape sella turcica": [ + "HP:0005723" + ], + "shoe - shaped sella turcica": [ + "HP:0005723" + ], + "nonopposable triphalangeal thumb": [ + "HP:0005725" + ], + "thumb hypoplastic with bulbous tip": [ + "HP:0005726" + ], + "thumbs hypoplastic with bulbous tips": [ + "HP:0005726" + ], + "short thumb with bulbous tip": [ + "HP:0005726" + ], + "short thumbs with bulbous tips": [ + "HP:0005726" + ], + "cortical irregularity": [ + "HP:0005731" + ], + "spinal stenosis with reduced interpedicular distance": [ + "HP:0005733" + ], + "spinal stenosis due to short pedicle": [ + "HP:0005733" + ], + "spinal stenosis due to short pedicles": [ + "HP:0005733" + ], + "short tibia": [ + "HP:0005736" + ], + "hypoplasia of the tibia": [ + "HP:0005736" + ], + "hypoplastic tibia": [ + "HP:0005736" + ], + "short shinbone": [ + "HP:0005736" + ], + "short skankbone": [ + "HP:0005736" + ], + "short tibiae": [ + "HP:0005736" + ], + "shortening of the shankbone": [ + "HP:0005736" + ], + "shortening of the shinbone": [ + "HP:0005736" + ], + "shortening of the tibia": [ + "HP:0005736" + ], + "posterior subluxation of radial head": [ + "HP:0005739" + ], + "avascular necrosis of the capital femoral epiphysis": [ + "HP:0005743" + ], + "coxa plana": [ + "HP:0005743" + ], + "legg - calve - perthes syndrome": [ + "HP:0005743" + ], + "legg - perthes disease": [ + "HP:0005743" + ], + "morbus legg - calve - perthes": [ + "HP:0005743" + ], + "osteochondrosis of the femoral head": [ + "HP:0005743" + ], + "osteonecrosis of the femoral head": [ + "HP:0005743" + ], + "perthes - like femoral head change": [ + "HP:0005743" + ], + "perthes - like femoral head changes": [ + "HP:0005743" + ], + "obsolete generalize osteoporosis with pathologic fracture": [ + "HP:0005744" + ], + "obsolete generalized osteoporosis with pathologic fractures": [ + "HP:0005744" + ], + "congenital foot contracture": [ + "HP:0005745" + ], + "congenital foot contractures": [ + "HP:0005745" + ], + "osteosclerosis of the base of the skull": [ + "HP:0005746" + ], + "osteosclerosis of the skull base": [ + "HP:0005746" + ], + "easily subluxate first metacarpophalangeal joint": [ + "HP:0005747" + ], + "easily subluxated first metacarpophalangeal joints": [ + "HP:0005747" + ], + "contracture of the joint of the low limb": [ + "HP:0005750" + ], + "contractures of the joints of the lower limbs": [ + "HP:0005750" + ], + "contracture , low limb": [ + "HP:0005750" + ], + "contractures , lower limbs": [ + "HP:0005750" + ], + "flatten moderately deformed vertebra": [ + "HP:0005752" + ], + "flattened moderately deformed vertebrae": [ + "HP:0005752" + ], + "neonatal epiphyseal stipple": [ + "HP:0005756" + ], + "neonatal epiphyseal stippling": [ + "HP:0005756" + ], + "epiphyseal stipple in neonate": [ + "HP:0005756" + ], + "epiphyseal stippling in neonates": [ + "HP:0005756" + ], + "speckled calcification in bone end part in neonate": [ + "HP:0005756" + ], + "speckled calcifications in bone end parts in neonates": [ + "HP:0005756" + ], + "basilar impression": [ + "HP:0005758" + ], + "small flat posterior fossa": [ + "HP:0005759" + ], + "small and flat posterior fossa of skull": [ + "HP:0005759" + ], + "small and flat posterior skull bone": [ + "HP:0005759" + ], + "small and flat posterior skull bones": [ + "HP:0005759" + ], + "polyarticular arthritis": [ + "HP:0005764" + ], + "sacral meningocele": [ + "HP:0005765" + ], + "disproportionate shortening of the tibia": [ + "HP:0005766" + ], + "disproportionate shortening of the shankbone": [ + "HP:0005766" + ], + "disproportionate shortening of the shinbone": [ + "HP:0005766" + ], + "marked shortening of tibia": [ + "HP:0005766" + ], + "1 - 2 toe complete cutaneous syndactyly": [ + "HP:0005767" + ], + "2 - 4 toe cutaneous syndactyly": [ + "HP:0005768" + ], + "soft tissue syndactyly of toe 2 , 3 , and 4": [ + "HP:0005768" + ], + "soft tissue syndactyly of toes 2 , 3 , and 4": [ + "HP:0005768" + ], + "webbed 2nd , 3rd and 4th toe": [ + "HP:0005768" + ], + "webbed 2nd , 3rd and 4th toes": [ + "HP:0005768" + ], + "webbed second , third and fourth toe": [ + "HP:0005768" + ], + "webbed second , third and fourth toes": [ + "HP:0005768" + ], + "fifth finger distal phalanx clinodactyly": [ + "HP:0005769" + ], + "curvature of outermost bone of little finger": [ + "HP:0005769" + ], + "curvature of outermost bone of pinkie finger": [ + "HP:0005769" + ], + "curvature of outermost bone of pinky finger": [ + "HP:0005769" + ], + "aplasia / hypoplasia of the tibia": [ + "HP:0005772" + ], + "absent / hypoplastic tibia": [ + "HP:0005772" + ], + "absent / small shankbone": [ + "HP:0005772" + ], + "absent / small shinbone": [ + "HP:0005772" + ], + "absent / underdevelop shankbone": [ + "HP:0005772" + ], + "absent / underdeveloped shankbone": [ + "HP:0005772" + ], + "absent / underdevelop shinbone": [ + "HP:0005772" + ], + "absent / underdeveloped shinbone": [ + "HP:0005772" + ], + "aplastic / hypoplastic tibia": [ + "HP:0005772" + ], + "short forearm": [ + "HP:0005773" + ], + "multiple skeletal anomaly": [ + "HP:0005775" + ], + "multiple skeletal anomalies": [ + "HP:0005775" + ], + "carpal bone malsegmentation": [ + "HP:0005776" + ], + "absent fourth finger distal interphalangeal crease": [ + "HP:0005780" + ], + "no fourth finger distal interphalangeal crease": [ + "HP:0005780" + ], + "contracture of the large joint": [ + "HP:0005781" + ], + "contractures of the large joints": [ + "HP:0005781" + ], + "lumbar platyspondyly": [ + "HP:0005787" + ], + "abnormal cervical myelogram": [ + "HP:0005788" + ], + "generalize osteosclerosis": [ + "HP:0005789" + ], + "generalized osteosclerosis": [ + "HP:0005789" + ], + "diffuse , symmetrical osteosclerosis": [ + "HP:0005789" + ], + "generalise osteosclerosis": [ + "HP:0005789" + ], + "generalised osteosclerosis": [ + "HP:0005789" + ], + "increase bone density in skeletal bone": [ + "HP:0005789" + ], + "increased bone density in skeletal bones": [ + "HP:0005789" + ], + "osteosclerosis , diffuse symmetrical": [ + "HP:0005789" + ], + "short mandibular condyle": [ + "HP:0005790" + ], + "short mandibular condyles": [ + "HP:0005790" + ], + "bilateral hypoplasia of condylar process of mandible": [ + "HP:0005790" + ], + "bilateral hypoplasia of mandibular condylar head": [ + "HP:0005790" + ], + "bilateral hypoplasia of mandibular condylar neck": [ + "HP:0005790" + ], + "decreased height of condylar process of mandible": [ + "HP:0005790" + ], + "decreased length of condylar process of mandible": [ + "HP:0005790" + ], + "short condylar head of mandible": [ + "HP:0005790" + ], + "short condylar neck of mandible": [ + "HP:0005790" + ], + "short condylar process of mandible": [ + "HP:0005790" + ], + "cortical thickening of long bone diaphysis": [ + "HP:0005791" + ], + "cortical thickening of long bone diaphyses": [ + "HP:0005791" + ], + "short humerus": [ + "HP:0005792" + ], + "humeral hypoplasia": [ + "HP:0005792" + ], + "humeral shortening": [ + "HP:0005792" + ], + "hypoplastic humerus": [ + "HP:0005792" + ], + "short humeri": [ + "HP:0005792" + ], + "short long bone of upper arm": [ + "HP:0005792" + ], + "short upper arm": [ + "HP:0005792" + ], + "short upper arms": [ + "HP:0005792" + ], + "shortening of all distal phalanx of the toe": [ + "HP:0005793" + ], + "shortening of all distal phalanges of the toes": [ + "HP:0005793" + ], + "shortening of all outermost bone of the toe": [ + "HP:0005793" + ], + "shortening of all outermost bone of the toes": [ + "HP:0005793" + ], + "obsolete arterial disease of leg": [ + "HP:0005794" + ], + "obsolete arterial disease of legs": [ + "HP:0005794" + ], + "posterior radial head dislocation": [ + "HP:0005798" + ], + "coalescence of tarsal bone": [ + "HP:0005802" + ], + "coalescence of tarsal bones": [ + "HP:0005802" + ], + "absent distal phalanx": [ + "HP:0005807" + ], + "absent distal phalanges": [ + "HP:0005807" + ], + "absent outermost digital bone": [ + "HP:0005807" + ], + "absent outermost digital bones": [ + "HP:0005807" + ], + "supernumerary rib": [ + "HP:0005815" + ], + "supernumerary ribs": [ + "HP:0005815" + ], + "extra rib": [ + "HP:0005815" + ], + "extra ribs": [ + "HP:0005815" + ], + "postaxial polysyndactyly of foot": [ + "HP:0005817" + ], + "short middle phalanx of finger": [ + "HP:0005819" + ], + "brachymesophalangy": [ + "HP:0005819" + ], + "disproportionately short middle phalanx": [ + "HP:0005819" + ], + "disproportionately short middle phalanges": [ + "HP:0005819" + ], + "hypoplasia of the middle phalanx of the hand": [ + "HP:0005819" + ], + "hypoplasia of the middle phalanges of the hand": [ + "HP:0005819" + ], + "hypoplastic middle phalanx": [ + "HP:0005819" + ], + "hypoplastic middle phalanges": [ + "HP:0005819" + ], + "midphalangeal hypoplasia": [ + "HP:0005819" + ], + "short middle bone of finger": [ + "HP:0005819" + ], + "short middle phalanx": [ + "HP:0005819" + ], + "short middle phalanges": [ + "HP:0005819" + ], + "shorten middle finger bone": [ + "HP:0005819" + ], + "shortened middle finger bones": [ + "HP:0005819" + ], + "superior rib anomaly": [ + "HP:0005820" + ], + "superior rib anomalies": [ + "HP:0005820" + ], + "clinodactyly of the 2nd toe": [ + "HP:0005824" + ], + "clinodactyly of second toe": [ + "HP:0005824" + ], + "clinodactyly of second toes": [ + "HP:0005824" + ], + "curvature of 2nd toe": [ + "HP:0005824" + ], + "mixed sclerosis of humeral metaphyses": [ + "HP:0005825" + ], + "transient pulmonary infiltrates": [ + "HP:0005828" + ], + "maldevelopment of radioulnar joint": [ + "HP:0005829" + ], + "flexion contracture of toe": [ + "HP:0005830" + ], + "contracture involve the toe": [ + "HP:0005830" + ], + "contractures involving the toes": [ + "HP:0005830" + ], + "contracture of the toe": [ + "HP:0005830" + ], + "contractures of the toes": [ + "HP:0005830" + ], + "toe contracture": [ + "HP:0005830" + ], + "toe contractures": [ + "HP:0005830" + ], + "type b brachydactyly": [ + "HP:0005831" + ], + "dysharmonic delay bone age": [ + "HP:0005832" + ], + "dysharmonic delayed bone age": [ + "HP:0005832" + ], + "obsolete joint swell onset late infancy": [ + "HP:0005833" + ], + "obsolete joint swelling onset late infancy": [ + "HP:0005833" + ], + "obsolete thumb hypo / aplastic": [ + "HP:0005834" + ], + "obsolete thumbs hypo / aplastic": [ + "HP:0005834" + ], + "obsolete joint dislocation in young adult": [ + "HP:0005837" + ], + "obsolete joint dislocations in young adult": [ + "HP:0005837" + ], + "calcific stippling of infantile cartilaginous skeleton": [ + "HP:0005841" + ], + "round middle phalanx of finger": [ + "HP:0005844" + ], + "rounded middle phalanx of finger": [ + "HP:0005844" + ], + "round middle bone of finger": [ + "HP:0005844" + ], + "rounded middle bone of finger": [ + "HP:0005844" + ], + "obsolete bifid thumb distal phalanx": [ + "HP:0005848" + ], + "diffuse cerebral calcification": [ + "HP:0005849" + ], + "congenital talipes calcaneovalgus": [ + "HP:0005850" + ], + "limited elbow extension and supination": [ + "HP:0005852" + ], + "congenital foot contraction deformity": [ + "HP:0005853" + ], + "congenital foot contraction deformities": [ + "HP:0005853" + ], + "multiple prenatal fracture": [ + "HP:0005855" + ], + "multiple prenatal fractures": [ + "HP:0005855" + ], + "congenital bone fracture": [ + "HP:0005855" + ], + "congenital bone fractures": [ + "HP:0005855" + ], + "multiple fracture present at birth": [ + "HP:0005855" + ], + "multiple fractures present at birth": [ + "HP:0005855" + ], + "multiple fracture , present at birth": [ + "HP:0005855" + ], + "multiple fractures , present at birth": [ + "HP:0005855" + ], + "numerous multiple fracture present at birth": [ + "HP:0005855" + ], + "numerous multiple fractures present at birth": [ + "HP:0005855" + ], + "numerous multiple fracture that be present at birth": [ + "HP:0005855" + ], + "numerous multiple fractures that are present at birth": [ + "HP:0005855" + ], + "ulnar radial head dislocation": [ + "HP:0005856" + ], + "ulnar dislocation of radial head": [ + "HP:0005856" + ], + "ulnar dislocation of radial heads": [ + "HP:0005856" + ], + "cervical spina bifida": [ + "HP:0005857" + ], + "type e brachydactyly": [ + "HP:0005863" + ], + "pseudoarthrosis": [ + "HP:0005864" + ], + "pseudoarthroses": [ + "HP:0005864" + ], + "opposable triphalangeal thumb": [ + "HP:0005866" + ], + "4 - 5 metacarpal synostosis": [ + "HP:0005867" + ], + "fuse 4th - 5th long bone of hand": [ + "HP:0005867" + ], + "fused 4th - 5th long bones of hand": [ + "HP:0005867" + ], + "fuse 4th - 5th metacarpal": [ + "HP:0005867" + ], + "fused 4th - 5th metacarpals": [ + "HP:0005867" + ], + "fuse fourth and fifth metacarpal": [ + "HP:0005867" + ], + "fused fourth and fifth metacarpals": [ + "HP:0005867" + ], + "ring finger and little finger metacarpal synostosis": [ + "HP:0005867" + ], + "synostosis of the fourth and fifth metacarpal bone": [ + "HP:0005867" + ], + "synostosis of the fourth and fifth metacarpal bones": [ + "HP:0005867" + ], + "metaphyseal enchondromatosis": [ + "HP:0005868" + ], + "metaphyseal chondrodysplasia": [ + "HP:0005871" + ], + "brachytelomesophalangy": [ + "HP:0005872" + ], + "progressive brachydactyly of middle and distal phalanx": [ + "HP:0005872" + ], + "progressive brachydactyly of middle and distal phalanges": [ + "HP:0005872" + ], + "short middle and distal phalanx of digit ii through v": [ + "HP:0005872" + ], + "short middle and distal phalanges of digits ii through v": [ + "HP:0005872" + ], + "polysyndactyly of hallux": [ + "HP:0005873" + ], + "polysyndactyly of big toe": [ + "HP:0005873" + ], + "polysyndactyly of great toe": [ + "HP:0005873" + ], + "increase dermatoglyphic whorl": [ + "HP:0005875" + ], + "increased dermatoglyphic whorls": [ + "HP:0005875" + ], + "progressive flexion contracture": [ + "HP:0005876" + ], + "progressive flexion contractures": [ + "HP:0005876" + ], + "joint contracture , progressive": [ + "HP:0005876" + ], + "joint contractures , progressive": [ + "HP:0005876" + ], + "multiple small vertebral fracture": [ + "HP:0005877" + ], + "multiple small vertebral fractures": [ + "HP:0005877" + ], + "enlarge sagittal diameter of the cervical canal": [ + "HP:0005878" + ], + "enlarged sagittal diameter of the cervical canal": [ + "HP:0005878" + ], + "congenital finger flexion contracture": [ + "HP:0005879" + ], + "congenital finger flexion contractures": [ + "HP:0005879" + ], + "congenital finger contracture": [ + "HP:0005879" + ], + "congenital finger contractures": [ + "HP:0005879" + ], + "metacarpophalangeal synostosis": [ + "HP:0005880" + ], + "fuse long bone of hand with innermost finger bone": [ + "HP:0005880" + ], + "fused long bone of hand with innermost finger bone": [ + "HP:0005880" + ], + "spinal instability": [ + "HP:0005881" + ], + "dermatoglyphic variant": [ + "HP:0005882" + ], + "dermatoglyphic variants": [ + "HP:0005882" + ], + "absent ossification of cervical vertebral body": [ + "HP:0005885" + ], + "absent ossification of cervical vertebral bodies": [ + "HP:0005885" + ], + "aphalangy of the hand": [ + "HP:0005886" + ], + "aphalangy of the hands": [ + "HP:0005886" + ], + "hyperostosis cranialis interna": [ + "HP:0005890" + ], + "enlargement of the inner surface of the skull bone": [ + "HP:0005890" + ], + "enlargement of the inner surface of the skull bones": [ + "HP:0005890" + ], + "excessive growth of inner surface of the skull bone": [ + "HP:0005890" + ], + "excessive growth of inner surface of the skull bones": [ + "HP:0005890" + ], + "hyperostosis of the internal surface of the cranial bone": [ + "HP:0005890" + ], + "hyperostosis of the internal surface of the cranial bones": [ + "HP:0005890" + ], + "hypertrophy of the internal surface of the cranial bone": [ + "HP:0005890" + ], + "hypertrophy of the internal surface of the cranial bones": [ + "HP:0005890" + ], + "increase ossification of the internal surface of the cranial bone": [ + "HP:0005890" + ], + "increased ossification of the internal surface of the cranial bones": [ + "HP:0005890" + ], + "overgrowth of the inner surface of the skull bone": [ + "HP:0005890" + ], + "overgrowth of the inner surface of the skull bones": [ + "HP:0005890" + ], + "overgrowth of the inside of the skull": [ + "HP:0005890" + ], + "thick inner surface of the skull bone": [ + "HP:0005890" + ], + "thick inner surface of the skull bones": [ + "HP:0005890" + ], + "thick internal surface of the cranial bone": [ + "HP:0005890" + ], + "thick internal surface of the cranial bones": [ + "HP:0005890" + ], + "progressive forearm bowing": [ + "HP:0005891" + ], + "progressive forearm curvature": [ + "HP:0005891" + ], + "proximal tibial and fibular fusion": [ + "HP:0005892" + ], + "fusion of innermost shinbone and calf bone": [ + "HP:0005892" + ], + "double first metacarpal": [ + "HP:0005894" + ], + "double first metacarpals": [ + "HP:0005894" + ], + "double 1st long bone of hand": [ + "HP:0005894" + ], + "double 1st long bones of hand": [ + "HP:0005894" + ], + "radial deviation of thumb terminal phalanx": [ + "HP:0005895" + ], + "severe generalize osteoporosis": [ + "HP:0005897" + ], + "severe generalized osteoporosis": [ + "HP:0005897" + ], + "severe generalise osteoporosis": [ + "HP:0005897" + ], + "severe generalised osteoporosis": [ + "HP:0005897" + ], + "severe , generalise osteoporosis": [ + "HP:0005897" + ], + "severe , generalised osteoporosis": [ + "HP:0005897" + ], + "severe , generalize osteoporosis": [ + "HP:0005897" + ], + "severe , generalized osteoporosis": [ + "HP:0005897" + ], + "metaphyseal dysostosis": [ + "HP:0005899" + ], + "fifth metacarpal with ulnar notch": [ + "HP:0005900" + ], + "fifth metacarpal notch on ulnar side": [ + "HP:0005900" + ], + "fifth metacarpal notched on ulnar side": [ + "HP:0005900" + ], + "obsolete chronic recurrent multifocal osteomyelitis": [ + "HP:0005901" + ], + "abnormal cervical curvature": [ + "HP:0005905" + ], + "abnormal neck curve": [ + "HP:0005905" + ], + "delay pneumatization of the mastoid process": [ + "HP:0005906" + ], + "delayed pneumatization of the mastoid process": [ + "HP:0005906" + ], + "mastoid process poorly pneumatized": [ + "HP:0005906" + ], + "mastoid processes poorly pneumatized": [ + "HP:0005906" + ], + "rhomboid or triangular shape 5th finger middle phalanx": [ + "HP:0005910" + ], + "rhomboid or triangular shaped 5th finger middle phalanx": [ + "HP:0005910" + ], + "rhomboid or triangular shape fifth finger middle phalanx": [ + "HP:0005910" + ], + "rhomboid or triangular shaped fifth finger middle phalanx": [ + "HP:0005910" + ], + "biliary atresia": [ + "HP:0005912" + ], + "biliary duct atresia": [ + "HP:0005912" + ], + "abnormality of metacarpal epiphysis": [ + "HP:0005913" + ], + "abnormality of metacarpal epiphyses": [ + "HP:0005913" + ], + "abnormality of end part of long bone of hand": [ + "HP:0005913" + ], + "aplasia / hypoplasia involve the metacarpal bone": [ + "HP:0005914" + ], + "aplasia / hypoplasia involving the metacarpal bones": [ + "HP:0005914" + ], + "absent or hypoplastic metacarpal": [ + "HP:0005914" + ], + "absent or hypoplastic metacarpals": [ + "HP:0005914" + ], + "absent / small long bone of hand": [ + "HP:0005914" + ], + "absent / small long bones of hand": [ + "HP:0005914" + ], + "absent / underdevelop long bone of hand": [ + "HP:0005914" + ], + "absent / underdeveloped long bones of hand": [ + "HP:0005914" + ], + "aplastic / hypoplastic metacarpal": [ + "HP:0005914" + ], + "aplastic / hypoplastic metacarpals": [ + "HP:0005914" + ], + "hypoplastic metacarpal": [ + "HP:0005914", + "HP:0010049" + ], + "hypoplastic metacarpals": [ + "HP:0005914" + ], + "hypoplastic / absent metacarpal bone": [ + "HP:0005914" + ], + "hypoplastic / absent metacarpal bones": [ + "HP:0005914" + ], + "hypoplastic / absent metacarpal": [ + "HP:0005914" + ], + "hypoplastic / absent metacarpals": [ + "HP:0005914" + ], + "metacarpal aplasia / hypoplasia": [ + "HP:0005914" + ], + "abnormal metacarpal morphology": [ + "HP:0005916" + ], + "abnormal shape of long bone of hand": [ + "HP:0005916" + ], + "abnormal shape of long bones of hand": [ + "HP:0005916" + ], + "abnormal shape of metacarpal bone": [ + "HP:0005916" + ], + "abnormal shape of metacarpal bones": [ + "HP:0005916" + ], + "supernumerary metacarpal bone": [ + "HP:0005917" + ], + "supernumerary metacarpal bones": [ + "HP:0005917" + ], + "extra long bone of hand": [ + "HP:0005917" + ], + "extra long bones of hand": [ + "HP:0005917" + ], + "abnormal finger phalanx morphology": [ + "HP:0005918" + ], + "abnormal form of phalanx of the hand": [ + "HP:0005918" + ], + "abnormal form of phalanges of the hand": [ + "HP:0005918" + ], + "abnormality of phalanx of finger": [ + "HP:0005918" + ], + "abnormality of the finger bone": [ + "HP:0005918" + ], + "abnormality of the finger bones": [ + "HP:0005918" + ], + "abnormality of the phalanx": [ + "HP:0005918" + ], + "abnormality of the phalanges": [ + "HP:0005918" + ], + "abnormality of the phalanx of the hand": [ + "HP:0005918" + ], + "abnormality of the phalanges of the hand": [ + "HP:0005918" + ], + "abnormal epiphysis morphology of the phalanx of the hand": [ + "HP:0005920" + ], + "abnormal epiphysis morphology of the phalanges of the hand": [ + "HP:0005920" + ], + "obsolete abnormal ossification of hand bone": [ + "HP:0005921" + ], + "obsolete abnormal ossification of hand bones": [ + "HP:0005921" + ], + "abnormal hand morphology": [ + "HP:0005922" + ], + "abnormal shape of hand": [ + "HP:0005922" + ], + "abnormality of the metaphyses of the hand": [ + "HP:0005923" + ], + "abnormalities of the metaphyses of the hand": [ + "HP:0005923" + ], + "abnormality of the wide portion of the hand bone": [ + "HP:0005923" + ], + "abnormality of the epiphysis of the hand": [ + "HP:0005924" + ], + "abnormality of the epiphyses of the hand": [ + "HP:0005924" + ], + "abnormality of the end part of the hand bone": [ + "HP:0005924" + ], + "abnormality of the end part of the hand bones": [ + "HP:0005924" + ], + "abnormality of the epiphysis of the finger": [ + "HP:0005924" + ], + "abnormality of the epiphyses of the fingers": [ + "HP:0005924" + ], + "abnormality of the epiphysis of the phalanx of the hand": [ + "HP:0005924" + ], + "abnormality of the epiphyses of the phalanges of the hand": [ + "HP:0005924" + ], + "abnormality of the diaphysis of the hand": [ + "HP:0005925" + ], + "abnormalities of the diaphyses of the hand": [ + "HP:0005925" + ], + "abnormality of shaft of long bone of the hand": [ + "HP:0005925" + ], + "abnormalities of shaft of long bone of the hand": [ + "HP:0005925" + ], + "abnormality of hand cortical bone": [ + "HP:0005926" + ], + "abnormality of the cortex of hand bone": [ + "HP:0005926" + ], + "abnormality of the cortex of hand bones": [ + "HP:0005926" + ], + "aplasia / hypoplasia involve bone of the hand": [ + "HP:0005927" + ], + "aplasia / hypoplasia involving bones of the hand": [ + "HP:0005927" + ], + "absent / small hand bone": [ + "HP:0005927" + ], + "absent / small hand bones": [ + "HP:0005927" + ], + "absent / underdeveloped hand bone": [ + "HP:0005927" + ], + "absent / underdeveloped hand bones": [ + "HP:0005927" + ], + "hypoplasia / absence of hand bone": [ + "HP:0005927" + ], + "hypoplasia / absence of hand bones": [ + "HP:0005927" + ], + "synostosis involve the fibula": [ + "HP:0005928" + ], + "synostosis involving the fibula": [ + "HP:0005928" + ], + "bone fusion involve the calf bone": [ + "HP:0005928" + ], + "bone fusion involving the calf bones": [ + "HP:0005928" + ], + "synostosis involve the tibia": [ + "HP:0005929" + ], + "synostosis involving the tibia": [ + "HP:0005929" + ], + "bone fusion involve the shinbone": [ + "HP:0005929" + ], + "bone fusion involving the shinbone": [ + "HP:0005929" + ], + "abnormality of epiphysis morphology": [ + "HP:0005930" + ], + "abnormal shape of end part of bone": [ + "HP:0005930" + ], + "abnormality of the epiphysis": [ + "HP:0005930" + ], + "abnormality of the epiphyses": [ + "HP:0005930" + ], + "anomaly of the epiphysis": [ + "HP:0005930" + ], + "anomaly of the epiphyses": [ + "HP:0005930" + ], + "epiphyseal abnormality": [ + "HP:0005930" + ], + "abnormal renal corticomedullary differentiation": [ + "HP:0005932" + ], + "imperfect vocal cord adduction": [ + "HP:0005934" + ], + "abnormal respiratory motile cilium morphology": [ + "HP:0005938" + ], + "multiple bilateral pneumothoraces": [ + "HP:0005939" + ], + "intermittent hyperpnea at rest": [ + "HP:0005941" + ], + "desquamative interstitial pneumonitis": [ + "HP:0005942" + ], + "filling of the alveolus with alveolar macrophage": [ + "HP:0005942" + ], + "filling of the alveoli with alveolar macrophages": [ + "HP:0005942" + ], + "filling of the alveolus with desquamated epithelial cell": [ + "HP:0005942" + ], + "filling of the alveoli with desquamated epithelial cells": [ + "HP:0005942" + ], + "intra - alveolar accumulation of macrophage": [ + "HP:0005942" + ], + "intra - alveolar accumulation of macrophages": [ + "HP:0005942" + ], + "respiratory arrest": [ + "HP:0005943" + ], + "breathe cessation": [ + "HP:0005943" + ], + "breathing cessation": [ + "HP:0005943" + ], + "bilateral lung agenesis": [ + "HP:0005944" + ], + "absent lung": [ + "HP:0005944" + ], + "absent lungs": [ + "HP:0005944" + ], + "bilateral pulmonary agenesis": [ + "HP:0005944" + ], + "laryngeal obstruction": [ + "HP:0005945" + ], + "ventilator dependence with inability to wean": [ + "HP:0005946" + ], + "decrease sensitivity to hypoxemia": [ + "HP:0005947" + ], + "decreased sensitivity to hypoxemia": [ + "HP:0005947" + ], + "decrease sensitivity to hypoxaemia": [ + "HP:0005947" + ], + "decreased sensitivity to hypoxaemia": [ + "HP:0005947" + ], + "multiple pulmonary cyst": [ + "HP:0005948" + ], + "multiple pulmonary cysts": [ + "HP:0005948" + ], + "cystic lung disease": [ + "HP:0005948" + ], + "multiple lung cyst": [ + "HP:0005948" + ], + "multiple lung cysts": [ + "HP:0005948" + ], + "apneic episode in infancy": [ + "HP:0005949" + ], + "apneic episodes in infancy": [ + "HP:0005949" + ], + "laryngeal web": [ + "HP:0005950" + ], + "laryngeal webs": [ + "HP:0005950" + ], + "partial laryngeal atresia": [ + "HP:0005950" + ], + "progressive inspiratory stridor": [ + "HP:0005951" + ], + "decrease pulmonary function": [ + "HP:0005952" + ], + "decreased pulmonary function": [ + "HP:0005952" + ], + "decrease lung function": [ + "HP:0005952" + ], + "decreased lung function": [ + "HP:0005952" + ], + "impaired lung function": [ + "HP:0005952" + ], + "impaired pulmonary function": [ + "HP:0005952" + ], + "pulmonary capillary hemangiomatosis": [ + "HP:0005954" + ], + "pulmonary hemangioma": [ + "HP:0005954" + ], + "pulmonary hemangiomas": [ + "HP:0005954" + ], + "anteroposteriorly shorten larynx": [ + "HP:0005956" + ], + "anteroposteriorly shortened larynx": [ + "HP:0005956" + ], + "breathe dysregulation": [ + "HP:0005957" + ], + "breathing dysregulation": [ + "HP:0005957" + ], + "impaired gluconeogenesis": [ + "HP:0005959" + ], + "gluconeogenesis impair": [ + "HP:0005959" + ], + "gluconeogenesis impaired": [ + "HP:0005959" + ], + "hypoargininemia": [ + "HP:0005961" + ], + "arginine deficiency": [ + "HP:0005961" + ], + "low blood arginine level": [ + "HP:0005961" + ], + "low blood arginine levels": [ + "HP:0005961" + ], + "intermittent hypothermia": [ + "HP:0005964" + ], + "intermittent abnormally low body temperature": [ + "HP:0005964" + ], + "mixed respiratory and metabolic acidosis": [ + "HP:0005967" + ], + "temperature instability": [ + "HP:0005968" + ], + "body temperature instability": [ + "HP:0005968" + ], + "respiratory acidosis": [ + "HP:0005972" + ], + "fructose intolerance": [ + "HP:0005973" + ], + "fructose malabsorption": [ + "HP:0005973" + ], + "episodic ketoacidosis": [ + "HP:0005974" + ], + "ketoacidosis , episodic": [ + "HP:0005974" + ], + "hyperkalemic metabolic acidosis": [ + "HP:0005976" + ], + "hypochloremic metabolic alkalosis": [ + "HP:0005977" + ], + "type ii diabetes mellitus": [ + "HP:0005978" + ], + "diabetes mellitus type 2": [ + "HP:0005978" + ], + "diabetes mellitus type ii": [ + "HP:0005978" + ], + "diabetes mellitus , noninsulin - dependent": [ + "HP:0005978" + ], + "niddm diabetes mellitus": [ + "HP:0005978" + ], + "non - insulin dependent diabetes": [ + "HP:0005978" + ], + "noninsulin dependent diabetes mellitus": [ + "HP:0005978" + ], + "noninsulin - dependent diabetes": [ + "HP:0005978" + ], + "noninsulin - dependent diabetes mellitus": [ + "HP:0005978" + ], + "type 2 diabetes": [ + "HP:0005978" + ], + "type ii diabetes": [ + "HP:0005978" + ], + "metabolic ketoacidosis": [ + "HP:0005979" + ], + "starvation ketoacidosis": [ + "HP:0005979" + ], + "reduce phenylalanine hydroxylase level": [ + "HP:0005982" + ], + "reduced phenylalanine hydroxylase level": [ + "HP:0005982" + ], + "phenylalanine hydroxylase deficiency": [ + "HP:0005982" + ], + "elevate maternal serum alpha - fetoprotein": [ + "HP:0005984" + ], + "elevated maternal serum alpha - fetoprotein": [ + "HP:0005984" + ], + "limitation of neck motion": [ + "HP:0005986" + ], + "limited neck mobility": [ + "HP:0005986" + ], + "restrict neck movement": [ + "HP:0005986" + ], + "restricted neck movement": [ + "HP:0005986" + ], + "multinodular goiter": [ + "HP:0005987" + ], + "multinodular goitre": [ + "HP:0005987" + ], + "congenital muscular torticollis": [ + "HP:0005988" + ], + "torticollis , congenital": [ + "HP:0005988" + ], + "redundant neck skin": [ + "HP:0005989" + ], + "excess neck skin": [ + "HP:0005989" + ], + "excess skin over the neck": [ + "HP:0005989" + ], + "excessive nuchal skin": [ + "HP:0005989" + ], + "redundant nuchal skin": [ + "HP:0005989" + ], + "redundant skin fold of neck": [ + "HP:0005989" + ], + "redundant skin folds of neck": [ + "HP:0005989" + ], + "redundant skin over the neck": [ + "HP:0005989" + ], + "thyroid hypoplasia": [ + "HP:0005990" + ], + "hypoplastic thyroid": [ + "HP:0005990" + ], + "small thyroid gland": [ + "HP:0005990" + ], + "limited neck flexion": [ + "HP:0005991" + ], + "limited cervical flexion": [ + "HP:0005991" + ], + "limited neck flexibility": [ + "HP:0005991" + ], + "nodular goiter": [ + "HP:0005994" + ], + "nodular goitre": [ + "HP:0005994" + ], + "decrease adipose tissue around neck": [ + "HP:0005995" + ], + "decreased adipose tissue around neck": [ + "HP:0005995" + ], + "loss of adipose tissue around the neck": [ + "HP:0005995" + ], + "loss of fat around neck": [ + "HP:0005995" + ], + "restrict neck movement due to contracture": [ + "HP:0005997" + ], + "restricted neck movement due to contractures": [ + "HP:0005997" + ], + "neck flexion contracture": [ + "HP:0005997" + ], + "restrict neck mobility due to contracture": [ + "HP:0005997" + ], + "restricted neck mobility due to contractures": [ + "HP:0005997" + ], + "ureteral atresia": [ + "HP:0005999" + ], + "ureteral obstruction": [ + "HP:0006000" + ], + "hypotrophy of the small hand muscle": [ + "HP:0006006" + ], + "hypotrophy of the small hand muscles": [ + "HP:0006006" + ], + "degeneration of small hand muscle": [ + "HP:0006006" + ], + "degeneration of small hand muscles": [ + "HP:0006006" + ], + "unilateral brachydactyly": [ + "HP:0006008" + ], + "short digit on one side": [ + "HP:0006008" + ], + "short digits on one side": [ + "HP:0006008" + ], + "broad phalanx": [ + "HP:0006009" + ], + "broad phalanges": [ + "HP:0006009" + ], + "wide digital bone": [ + "HP:0006009" + ], + "wide digital bones": [ + "HP:0006009" + ], + "wide phalanx": [ + "HP:0006009" + ], + "wide phalanges": [ + "HP:0006009" + ], + "widen phalanx": [ + "HP:0006009" + ], + "widened phalanges": [ + "HP:0006009" + ], + "cuboidal metacarpal": [ + "HP:0006011" + ], + "short , cube shape long bone of hand": [ + "HP:0006011" + ], + "short , cube shaped long bone of hand": [ + "HP:0006011" + ], + "widen metacarpal shaft": [ + "HP:0006012" + ], + "widened metacarpal shaft": [ + "HP:0006012" + ], + "broad shaft of long bone of hand": [ + "HP:0006012" + ], + "abnormally shape carpal bone": [ + "HP:0006014" + ], + "abnormally shaped carpal bones": [ + "HP:0006014" + ], + "abnormally shaped wrist bone": [ + "HP:0006014" + ], + "abnormally shaped wrist bones": [ + "HP:0006014" + ], + "delay phalangeal epiphyseal ossification": [ + "HP:0006016" + ], + "delayed phalangeal epiphyseal ossification": [ + "HP:0006016" + ], + "delay bone maturation of end part of digital bone": [ + "HP:0006016" + ], + "delayed bone maturation of end part of digital bone": [ + "HP:0006016" + ], + "delay phalangeal epiphyseal bone maturation": [ + "HP:0006016" + ], + "delayed phalangeal epiphyseal bone maturation": [ + "HP:0006016" + ], + "reduce proximal interphalangeal joint space": [ + "HP:0006019" + ], + "reduced proximal interphalangeal joint space": [ + "HP:0006019" + ], + "decreased space in hinge joint": [ + "HP:0006019" + ], + "round epiphysis": [ + "HP:0006026" + ], + "rounded epiphyses": [ + "HP:0006026" + ], + "rounded end part of bone": [ + "HP:0006026" + ], + "metaphyseal cupping of metacarpal": [ + "HP:0006028" + ], + "metaphyseal cupping of metacarpals": [ + "HP:0006028" + ], + "cupping of wide portion of long bone of hand": [ + "HP:0006028" + ], + "metacarpal / metaphyseal cup": [ + "HP:0006028" + ], + "metacarpal / metaphyseal cupping": [ + "HP:0006028" + ], + "cone - shaped epiphysis of phalanx 2 to 5": [ + "HP:0006035" + ], + "cone - shaped epiphyses of phalanges 2 to 5": [ + "HP:0006035" + ], + "cone - shaped end part of digital bone 2 to 5": [ + "HP:0006035" + ], + "cone - shaped end part of digital bones 2 to 5": [ + "HP:0006035" + ], + "long second metacarpal": [ + "HP:0006040" + ], + "long 2nd long bone of hand": [ + "HP:0006040" + ], + "y - shape metacarpal": [ + "HP:0006042" + ], + "y - shaped metacarpals": [ + "HP:0006042" + ], + "y - shape long bone of hand": [ + "HP:0006042" + ], + "y - shaped long bone of hand": [ + "HP:0006042" + ], + "short point phalanx": [ + "HP:0006045" + ], + "short pointed phalanges": [ + "HP:0006045" + ], + "short point digital bone": [ + "HP:0006045" + ], + "short pointed digital bones": [ + "HP:0006045" + ], + "distal widening of metacarpal": [ + "HP:0006048" + ], + "distal widening of metacarpals": [ + "HP:0006048" + ], + "wide outermost end of long bone": [ + "HP:0006048" + ], + "metacarpal periosteal thicken": [ + "HP:0006051" + ], + "metacarpal periosteal thickening": [ + "HP:0006051" + ], + "ulnar deviate club hand": [ + "HP:0006055" + ], + "ulnar deviated club hands": [ + "HP:0006055" + ], + "cone - shape metacarpal epiphysis": [ + "HP:0006059" + ], + "cone - shaped metacarpal epiphyses": [ + "HP:0006059" + ], + "cone - shaped end part of long bone": [ + "HP:0006059" + ], + "metacarpal cone - shaped epiphysis": [ + "HP:0006059" + ], + "metacarpal cone - shaped epiphyses": [ + "HP:0006059" + ], + "tombstone - shape proximal phalanx": [ + "HP:0006060" + ], + "tombstone - shaped proximal phalanges": [ + "HP:0006060" + ], + "tombstone - shape innermost digital bone": [ + "HP:0006060" + ], + "tombstone - shaped innermost digital bones": [ + "HP:0006060" + ], + "limited interphalangeal movement": [ + "HP:0006064" + ], + "limited movement of hinge joint": [ + "HP:0006064" + ], + "limited movement of hinge joints": [ + "HP:0006064" + ], + "multiple carpal ossification center": [ + "HP:0006067" + ], + "multiple carpal ossification centers": [ + "HP:0006067" + ], + "multiple carpal ossification centre": [ + "HP:0006067" + ], + "multiple carpal ossification centres": [ + "HP:0006067" + ], + "severe carpal ossification delay": [ + "HP:0006069" + ], + "severe delay in maturation of wrist bone": [ + "HP:0006069" + ], + "metacarpophalangeal joint contracture": [ + "HP:0006070" + ], + "metacarpal / phalangeal joint contracture": [ + "HP:0006070" + ], + "metacarpal / phalangeal joint contractures": [ + "HP:0006070" + ], + "absent proximal finger flexion crease": [ + "HP:0006077" + ], + "absent proximal finger flexion creases": [ + "HP:0006077" + ], + "thin metacarpal cortex": [ + "HP:0006086" + ], + "thin metacarpal cortices": [ + "HP:0006086" + ], + "1 - 5 finger complete cutaneous syndactyly": [ + "HP:0006088" + ], + "palmar hyperhidrosis": [ + "HP:0006089" + ], + "excessive sweating of hand": [ + "HP:0006089" + ], + "excessive sweating of hands": [ + "HP:0006089" + ], + "malaligned carpal bone": [ + "HP:0006092" + ], + "incorrect alignment of wrist bone": [ + "HP:0006092" + ], + "finger joint hypermobility": [ + "HP:0006094" + ], + "increase mobility in finger joint": [ + "HP:0006094" + ], + "increased mobility in finger joint": [ + "HP:0006094" + ], + "wide tuft of distal phalanx": [ + "HP:0006095" + ], + "wide tufts of distal phalanges": [ + "HP:0006095" + ], + "wide tip of outermost digital bone": [ + "HP:0006095" + ], + "wide tips of outermost digital bone": [ + "HP:0006095" + ], + "3 - 4 finger syndactyly": [ + "HP:0006097" + ], + "partial or complete syndactyly 3rd - 4th finger": [ + "HP:0006097" + ], + "partial or complete syndactyly 3rd - 4th fingers": [ + "HP:0006097" + ], + "web 3rd - 4th finger": [ + "HP:0006097" + ], + "webbed 3rd - 4th finger": [ + "HP:0006097" + ], + "webbed 3rd - 4th fingers": [ + "HP:0006097" + ], + "metacarpophalangeal joint hyperextensibility": [ + "HP:0006099" + ], + "finger syndactyly": [ + "HP:0006101" + ], + "partial syndactyly": [ + "HP:0006101" + ], + "absent trapezoid bone": [ + "HP:0006106" + ], + "fingerpad telangiectases": [ + "HP:0006107" + ], + "finger pad telangiectases": [ + "HP:0006107" + ], + "small dilate blood vessel in fingerpads": [ + "HP:0006107" + ], + "small dilated blood vessels in fingerpads": [ + "HP:0006107" + ], + "taper metacarpal": [ + "HP:0006108" + ], + "tapered metacarpals": [ + "HP:0006108" + ], + "taper long bone of hand": [ + "HP:0006108" + ], + "tapered long bones of hand": [ + "HP:0006108" + ], + "absent phalangeal crease": [ + "HP:0006109" + ], + "absent interphalangeal crease": [ + "HP:0006109" + ], + "absent interphalangeal creases": [ + "HP:0006109" + ], + "aplasia of the interphalangeal crease": [ + "HP:0006109" + ], + "aplasia of the interphalangeal creases": [ + "HP:0006109" + ], + "shortening of all middle phalanx of the finger": [ + "HP:0006110" + ], + "shortening of all middle phalanges of the fingers": [ + "HP:0006110" + ], + "expand phalanx with widened medullary cavity": [ + "HP:0006112" + ], + "expanded phalanges with widened medullary cavities": [ + "HP:0006112" + ], + "multiple palmar crease": [ + "HP:0006114" + ], + "multiple palmar creases": [ + "HP:0006114" + ], + "multiple palm line": [ + "HP:0006114" + ], + "multiple palm lines": [ + "HP:0006114" + ], + "shortening of all distal phalanx of the finger": [ + "HP:0006118" + ], + "shortening of all distal phalanges of the fingers": [ + "HP:0006118" + ], + "brachytelephalangy": [ + "HP:0006118" + ], + "shortening of all outermost bone of the finger": [ + "HP:0006118" + ], + "shortening of all outermost bones of the fingers": [ + "HP:0006118" + ], + "proximal tapering of metacarpal": [ + "HP:0006119" + ], + "proximal tapering of metacarpals": [ + "HP:0006119" + ], + "point innermost long bone of hand": [ + "HP:0006119" + ], + "pointed innermost long bone of hand": [ + "HP:0006119" + ], + "point proximal metacarpal": [ + "HP:0006119" + ], + "pointed proximal metacarpals": [ + "HP:0006119" + ], + "acral ulceration": [ + "HP:0006121" + ], + "long proximal phalanx of finger": [ + "HP:0006127" + ], + "long innermost finger bone": [ + "HP:0006127" + ], + "drumstick terminal phalanx": [ + "HP:0006129" + ], + "drumstick terminal phalanges": [ + "HP:0006129" + ], + "drumstick shape digital bone": [ + "HP:0006129" + ], + "drumstick shaped digital bones": [ + "HP:0006129" + ], + "enlarge metacarpal epiphysis": [ + "HP:0006134" + ], + "enlarged metacarpal epiphyses": [ + "HP:0006134" + ], + "enlarged end part of long bone of hand": [ + "HP:0006134" + ], + "decrease finger mobility": [ + "HP:0006135" + ], + "decreased finger mobility": [ + "HP:0006135" + ], + "decrease finger movement": [ + "HP:0006135" + ], + "decreased finger movement": [ + "HP:0006135" + ], + "bilateral postaxial polydactyly": [ + "HP:0006136" + ], + "premature fusion of phalangeal epiphysis": [ + "HP:0006140" + ], + "premature fusion of phalangeal epiphyses": [ + "HP:0006140" + ], + "premature fusion of end part of digital bone": [ + "HP:0006140" + ], + "abnormal finger flexion crease": [ + "HP:0006143" + ], + "abnormal finger flexion creases": [ + "HP:0006143" + ], + "shortening of all proximal phalanx of the finger": [ + "HP:0006144" + ], + "shortening of all proximal phalanges of the fingers": [ + "HP:0006144" + ], + "shortening of all innermost bone of the finger": [ + "HP:0006144" + ], + "shortening of all innermost bones of the fingers": [ + "HP:0006144" + ], + "central y - shape metacarpal": [ + "HP:0006145" + ], + "central y - shaped metacarpal": [ + "HP:0006145" + ], + "y - shaped central long bone of hand": [ + "HP:0006145" + ], + "y - shaped central long bones of hand": [ + "HP:0006145" + ], + "broad metacarpal epiphysis": [ + "HP:0006146" + ], + "broad metacarpal epiphyses": [ + "HP:0006146" + ], + "broad end part of long bone of hand": [ + "HP:0006146" + ], + "progressive fusion 2nd - 5th pip joint": [ + "HP:0006147" + ], + "progressive fusion 2nd - 5th pip joints": [ + "HP:0006147" + ], + "increase laxity of finger": [ + "HP:0006149" + ], + "increased laxity of fingers": [ + "HP:0006149" + ], + "swan neck - like deformity of the finger": [ + "HP:0006150" + ], + "swan neck - like deformities of the fingers": [ + "HP:0006150" + ], + "proximal symphalangism of hand": [ + "HP:0006152" + ], + "proximal symphalangism of hands": [ + "HP:0006152" + ], + "fuse innermost hinge joint": [ + "HP:0006152" + ], + "fused innermost hinge joints": [ + "HP:0006152" + ], + "proximal interphalangeal joint synostoses": [ + "HP:0006152" + ], + "disharmonious carpal bone": [ + "HP:0006153" + ], + "disharmonious wrist bone": [ + "HP:0006153" + ], + "long phalanx of finger": [ + "HP:0006155" + ], + "long finger bone": [ + "HP:0006155" + ], + "ulnar deviation of thumb": [ + "HP:0006156" + ], + "curve thumb deviate towards palm": [ + "HP:0006156" + ], + "curved thumb deviated towards palm": [ + "HP:0006156" + ], + "ulnar deviation of the 1st finger": [ + "HP:0006156" + ], + "prominent palmar flexion crease": [ + "HP:0006157" + ], + "prominent palmar flexion creases": [ + "HP:0006157" + ], + "prominent life line": [ + "HP:0006157" + ], + "obsolete finger joint hyperextensibility": [ + "HP:0006158" + ], + "mesoaxial hand polydactyly": [ + "HP:0006159" + ], + "central hand polydactyly": [ + "HP:0006159" + ], + "interdigital finger polydactyly": [ + "HP:0006159" + ], + "irregular metacarpal": [ + "HP:0006160" + ], + "irregular metacarpals": [ + "HP:0006160" + ], + "irregular long bone of hand": [ + "HP:0006160" + ], + "irregular long bones of hand": [ + "HP:0006160" + ], + "short metacarpal with rounded proximal end": [ + "HP:0006161" + ], + "short metacarpals with rounded proximal ends": [ + "HP:0006161" + ], + "short long bone of hand with rounded innermost end": [ + "HP:0006161" + ], + "short long bone of hand with rounded innermost ends": [ + "HP:0006161" + ], + "soft tissue swelling of interphalangeal joint": [ + "HP:0006162" + ], + "soft tissue swelling of interphalangeal joints": [ + "HP:0006162" + ], + "soft tissue swelling of hinge joint": [ + "HP:0006162" + ], + "soft tissue swelling of hinge joints": [ + "HP:0006162" + ], + "enlarge metacarpophalangeal joint": [ + "HP:0006163" + ], + "enlarged metacarpophalangeal joints": [ + "HP:0006163" + ], + "proportionate shortening of all digit": [ + "HP:0006165" + ], + "proportionate shortening of all digits": [ + "HP:0006165" + ], + "tubular metacarpal bone": [ + "HP:0006166" + ], + "tubular metacarpal bones": [ + "HP:0006166" + ], + "cylindrical shape long bone of hand": [ + "HP:0006166" + ], + "cylindrical shaped long bones of hand": [ + "HP:0006166" + ], + "prominent proximal interphalangeal joint": [ + "HP:0006167" + ], + "prominent proximal interphalangeal joints": [ + "HP:0006167" + ], + "prominent innermost hinge joint": [ + "HP:0006167" + ], + "prominent innermost hinge joints": [ + "HP:0006167" + ], + "decrease mobility 3rd - 5th finger": [ + "HP:0006169" + ], + "decreased mobility 3rd - 5th fingers": [ + "HP:0006169" + ], + "chess - pawn distal phalanx": [ + "HP:0006170" + ], + "chess - pawn distal phalanges": [ + "HP:0006170" + ], + "chess - pawn shape outermost bone": [ + "HP:0006170" + ], + "chess - pawn shaped outermost bone": [ + "HP:0006170" + ], + "flatten , square - off epiphysis of tubular bone": [ + "HP:0006172" + ], + "flattened , squared - off epiphyses of tubular bones": [ + "HP:0006172" + ], + "flatten , square - off end part of tubular bone": [ + "HP:0006172" + ], + "flattened , squared - off end part of tubular bones": [ + "HP:0006172" + ], + "metacarpal diaphyseal endosteal sclerosis": [ + "HP:0006174" + ], + "proximal phalangeal periosteal thicken": [ + "HP:0006175" + ], + "proximal phalangeal periosteal thickening": [ + "HP:0006175" + ], + "thickening of connective tissue of innermost finger bone": [ + "HP:0006175" + ], + "two carpal ossification center present at birth": [ + "HP:0006176" + ], + "two carpal ossification centers present at birth": [ + "HP:0006176" + ], + "two carpal ossification centre present at birth": [ + "HP:0006176" + ], + "two carpal ossification centres present at birth": [ + "HP:0006176" + ], + "pseudoepiphyses of second metacarpal": [ + "HP:0006179" + ], + "extra bone on end of second long bone of hand": [ + "HP:0006179" + ], + "pseudoepiphysis of the 2nd metacarpal": [ + "HP:0006179" + ], + "crowd carpal bone": [ + "HP:0006180" + ], + "crowded carpal bones": [ + "HP:0006180" + ], + "crowd wrist bone": [ + "HP:0006180" + ], + "crowded wrist bones": [ + "HP:0006180" + ], + "decrease palmar crease": [ + "HP:0006184" + ], + "decreased palmar creases": [ + "HP:0006184" + ], + "hypoplastic palmar crease": [ + "HP:0006184" + ], + "hypoplastic palmar creases": [ + "HP:0006184" + ], + "poorly form palmar crease": [ + "HP:0006184" + ], + "poorly formed palmar creases": [ + "HP:0006184" + ], + "shallow palm line": [ + "HP:0006184" + ], + "shallow palmar crease": [ + "HP:0006184" + ], + "shallow palmar creases": [ + "HP:0006184" + ], + "enlarge proximal interphalangeal joint": [ + "HP:0006185" + ], + "enlarged proximal interphalangeal joints": [ + "HP:0006185" + ], + "enlarge innermost hinge joint": [ + "HP:0006185" + ], + "enlarged innermost hinge joint": [ + "HP:0006185" + ], + "fusion of midphalangeal joint": [ + "HP:0006187" + ], + "fusion of midphalangeal joints": [ + "HP:0006187" + ], + "prominent interdigital fold": [ + "HP:0006189" + ], + "prominent interdigital folds": [ + "HP:0006189" + ], + "radially deviate wrist": [ + "HP:0006190" + ], + "radially deviated wrists": [ + "HP:0006190" + ], + "deep palmar crease": [ + "HP:0006191" + ], + "deep palm line": [ + "HP:0006191" + ], + "deep palmar creases": [ + "HP:0006191" + ], + "tapered phalanx of finger": [ + "HP:0006192" + ], + "taper finger bone": [ + "HP:0006192" + ], + "tapered finger bone": [ + "HP:0006192" + ], + "thimble - shape middle phalanx of hand": [ + "HP:0006193" + ], + "thimble - shaped middle phalanges of hand": [ + "HP:0006193" + ], + "thimble - shape middle bone of hand": [ + "HP:0006193" + ], + "thimble - shaped middle bones of hand": [ + "HP:0006193" + ], + "widen distal phalanx": [ + "HP:0006200" + ], + "widened distal phalanges": [ + "HP:0006200" + ], + "widen outermost bone of limb": [ + "HP:0006200" + ], + "widened outermost bone of limb": [ + "HP:0006200" + ], + "hypermobility of distal interphalangeal joint": [ + "HP:0006201" + ], + "hypermobility of distal interphalangeal joints": [ + "HP:0006201" + ], + "increase mobility of outermost hinge joint": [ + "HP:0006201" + ], + "increased mobility of outermost hinge joint": [ + "HP:0006201" + ], + "osteolysis of scaphoids": [ + "HP:0006202" + ], + "decrease movement range in interphalangeal joint": [ + "HP:0006203" + ], + "decreased movement range in interphalangeal joints": [ + "HP:0006203" + ], + "decreased range of movement range in hinge joint": [ + "HP:0006203" + ], + "decreased range of movement range in hinge joints": [ + "HP:0006203" + ], + "irregular phalanx": [ + "HP:0006205" + ], + "irregular phalanges": [ + "HP:0006205" + ], + "irregular finger bone": [ + "HP:0006205" + ], + "irregular finger bones": [ + "HP:0006205" + ], + "hypersegmentation of proximal phalanx of second finger": [ + "HP:0006206" + ], + "partial fusion of carpal": [ + "HP:0006207" + ], + "partial fusion of carpals": [ + "HP:0006207" + ], + "metaphyseal cupping of proximal phalanx": [ + "HP:0006208" + ], + "metaphyseal cupping of proximal phalanges": [ + "HP:0006208" + ], + "partial - complete absence of 5th phalanx": [ + "HP:0006209" + ], + "partial - complete absence of 5th phalanges": [ + "HP:0006209" + ], + "partial - complete absence of 5th digital bone": [ + "HP:0006209" + ], + "postaxial oligodactyly": [ + "HP:0006210" + ], + "thin proximal phalanx with broad epiphysis of the hand": [ + "HP:0006213" + ], + "thin proximal phalanges with broad epiphyses of the hand": [ + "HP:0006213" + ], + "thin innermost bone with broad end part of the hand bone": [ + "HP:0006213" + ], + "thin proximal phalanx with broad epiphysis": [ + "HP:0006213" + ], + "thin proximal phalanges with broad epiphyses": [ + "HP:0006213" + ], + "single interphalangeal crease of fifth finger": [ + "HP:0006216" + ], + "fifth finger single interphalangeal crease": [ + "HP:0006216" + ], + "limited mobility of proximal interphalangeal joint": [ + "HP:0006217" + ], + "limited mobility of innermost hinge joint": [ + "HP:0006217" + ], + "taper point end of distal finger phalanx": [ + "HP:0006224" + ], + "tapering pointed ends of distal finger phalanges": [ + "HP:0006224" + ], + "osteoarthritis of the first carpometacarpal joint": [ + "HP:0006226" + ], + "valgus hand deformity": [ + "HP:0006228" + ], + "unilateral oligodactyly": [ + "HP:0006230" + ], + "expand metacarpal with widened medullary cavity": [ + "HP:0006232" + ], + "expanded metacarpals with widened medullary cavities": [ + "HP:0006232" + ], + "osteoarthritis of the distal interphalangeal joint": [ + "HP:0006233" + ], + "osteolysis involve tarsal bone": [ + "HP:0006234" + ], + "osteolysis involving tarsal bones": [ + "HP:0006234" + ], + "tarsal bone osteolysis": [ + "HP:0006234" + ], + "tarsal osteolysis": [ + "HP:0006234" + ], + "slender metacarpal": [ + "HP:0006236" + ], + "slender metacarpals": [ + "HP:0006236" + ], + "slender long bone of hand": [ + "HP:0006236" + ], + "slender long bones of hand": [ + "HP:0006236" + ], + "prominent interphalangeal joint": [ + "HP:0006237" + ], + "prominent interphalangeal joints": [ + "HP:0006237" + ], + "prominent hinge joint": [ + "HP:0006237" + ], + "prominent hinge joints": [ + "HP:0006237" + ], + "shortening of all middle phalanx of the toe": [ + "HP:0006239" + ], + "shortening of all middle phalanges of the toes": [ + "HP:0006239" + ], + "brachymesophalangy of foot": [ + "HP:0006239" + ], + "brachymesophalangy of feet": [ + "HP:0006239" + ], + "shortening of all the middle bone of the toe": [ + "HP:0006239" + ], + "shortening of all the middle bones of the toes": [ + "HP:0006239" + ], + "phalangeal dislocation": [ + "HP:0006243" + ], + "enlarge interphalangeal joint": [ + "HP:0006247" + ], + "enlarged interphalangeal joints": [ + "HP:0006247" + ], + "enlarged hinge joint": [ + "HP:0006247" + ], + "enlarged hinge joints": [ + "HP:0006247" + ], + "limited wrist movement": [ + "HP:0006248" + ], + "limited movement of the wrist": [ + "HP:0006248" + ], + "limited wrist extension": [ + "HP:0006251" + ], + "interphalangeal joint erosion": [ + "HP:0006252" + ], + "interphalangeal joint erosions": [ + "HP:0006252" + ], + "swell of proximal interphalangeal joint": [ + "HP:0006253" + ], + "swelling of proximal interphalangeal joints": [ + "HP:0006253" + ], + "swell of innermost hinge joint": [ + "HP:0006253" + ], + "swelling of innermost hinge joints": [ + "HP:0006253" + ], + "elevate alpha - fetoprotein": [ + "HP:0006254" + ], + "elevated alpha - fetoprotein": [ + "HP:0006254" + ], + "alpha fetoprotein abnormal": [ + "HP:0006254" + ], + "increased level of alpha fetoprotein": [ + "HP:0006254" + ], + "increased levels of alpha fetoprotein": [ + "HP:0006254" + ], + "increase serum alpha - fetoprotein": [ + "HP:0006254" + ], + "increased serum alpha - fetoprotein": [ + "HP:0006254" + ], + "serum alpha - fetoprotein increase": [ + "HP:0006254" + ], + "serum alpha - fetoprotein increased": [ + "HP:0006254" + ], + "abnormality of hand joint mobility": [ + "HP:0006256" + ], + "abnormality of carpal bone ossification": [ + "HP:0006257" + ], + "abnormal ankle bone maturation": [ + "HP:0006257" + ], + "abnormal phalangeal joint morphology of the hand": [ + "HP:0006261" + ], + "abnormality of phalangeal joint of the hand": [ + "HP:0006261" + ], + "abnormality of phalangeal joints of the hand": [ + "HP:0006261" + ], + "abnormality of the small joint of the hand": [ + "HP:0006261" + ], + "abnormality of the small joints of the hand": [ + "HP:0006261" + ], + "aplasia / hypoplasia of the 5th finger": [ + "HP:0006262" + ], + "absent / small little finger": [ + "HP:0006262" + ], + "absent / small pinkie finger": [ + "HP:0006262" + ], + "absent / small pinky finger": [ + "HP:0006262" + ], + "absent / underdevelop little finger": [ + "HP:0006262" + ], + "absent / underdeveloped little finger": [ + "HP:0006262" + ], + "absent / underdevelop pinkie finger": [ + "HP:0006262" + ], + "absent / underdeveloped pinkie finger": [ + "HP:0006262" + ], + "absent / underdevelop pinky finger": [ + "HP:0006262" + ], + "absent / underdeveloped pinky finger": [ + "HP:0006262" + ], + "abnormality of the epiphysis of the 2nd finger": [ + "HP:0006263" + ], + "abnormality of the epiphyses of the 2nd finger": [ + "HP:0006263" + ], + "abnormality of the end part of the index finger bone": [ + "HP:0006263" + ], + "aplasia / hypoplasia of the 2nd finger": [ + "HP:0006264" + ], + "absent / small index finger": [ + "HP:0006264" + ], + "absent / underdevelop index finger": [ + "HP:0006264" + ], + "absent / underdeveloped index finger": [ + "HP:0006264" + ], + "aplasia / hypoplasia of finger": [ + "HP:0006265" + ], + "aplasia / hypoplasia of fingers": [ + "HP:0006265" + ], + "absent / small finger": [ + "HP:0006265" + ], + "absent / small fingers": [ + "HP:0006265" + ], + "absent / underdevelop finger": [ + "HP:0006265" + ], + "absent / underdeveloped fingers": [ + "HP:0006265" + ], + "small placenta": [ + "HP:0006266" + ], + "large placenta": [ + "HP:0006267" + ], + "placental enlargement": [ + "HP:0006267" + ], + "fluctuate splenomegaly": [ + "HP:0006268" + ], + "fluctuating splenomegaly": [ + "HP:0006268" + ], + "hypoplastic spleen": [ + "HP:0006270" + ], + "underdeveloped spleen": [ + "HP:0006270" + ], + "pancreatic lymphangiectasis": [ + "HP:0006273" + ], + "reduce pancreatic beta cell": [ + "HP:0006274" + ], + "reduced pancreatic beta cells": [ + "HP:0006274" + ], + "hyperechogenic pancreas": [ + "HP:0006276" + ], + "pancreatic hyperplasia": [ + "HP:0006277" + ], + "ectopic pancreatic tissue": [ + "HP:0006278" + ], + "abnormal pancreas location": [ + "HP:0006278" + ], + "beta - cell dysfunction": [ + "HP:0006279" + ], + "chronic pancreatitis": [ + "HP:0006280" + ], + "chronic pancreas inflammation": [ + "HP:0006280" + ], + "generalize hypoplasia of dental enamel": [ + "HP:0006282" + ], + "generalized hypoplasia of dental enamel": [ + "HP:0006282" + ], + "generalised dysplasia of tooth enamel": [ + "HP:0006282" + ], + "generalised hypoplasia of dental enamel": [ + "HP:0006282" + ], + "generalised hypoplasia of tooth enamel": [ + "HP:0006282" + ], + "generalize dysplasia of tooth enamel": [ + "HP:0006282" + ], + "generalized dysplasia of tooth enamel": [ + "HP:0006282" + ], + "generalize hypoplasia of tooth enamel": [ + "HP:0006282" + ], + "generalized hypoplasia of tooth enamel": [ + "HP:0006282" + ], + "multiple unerupted teeth": [ + "HP:0006283" + ], + "failure of eruption of multiple teeth": [ + "HP:0006283" + ], + "multiple non - erupt teeth": [ + "HP:0006283" + ], + "multiple non - erupting teeth": [ + "HP:0006283" + ], + "enamel hypomineralization": [ + "HP:0006285" + ], + "decrease enamel mineralisation": [ + "HP:0006285" + ], + "decreased enamel mineralisation": [ + "HP:0006285" + ], + "fluorosis of tooth enamel": [ + "HP:0006285" + ], + "hypomineralization of enamel": [ + "HP:0006285" + ], + "increase porosity of tooth enamel": [ + "HP:0006285" + ], + "increased porosity of tooth enamel": [ + "HP:0006285" + ], + "mottle tooth enamel": [ + "HP:0006285" + ], + "mottled tooth enamel": [ + "HP:0006285" + ], + "poorly mineralize tooth enamel": [ + "HP:0006285" + ], + "poorly mineralized tooth enamel": [ + "HP:0006285" + ], + "white spot lesion of tooth enamel": [ + "HP:0006285" + ], + "white spot lesions of tooth enamel": [ + "HP:0006285" + ], + "yellow - brown discoloration of the teeth": [ + "HP:0006286" + ], + "yellow - brown discolor teeth": [ + "HP:0006286" + ], + "yellow - brown discolored teeth": [ + "HP:0006286" + ], + "yellow - brown discolour teeth": [ + "HP:0006286" + ], + "yellow - brown discoloured teeth": [ + "HP:0006286" + ], + "yellow - brown tooth shade": [ + "HP:0006286" + ], + "advanced eruption of teeth": [ + "HP:0006288" + ], + "advanced dental eruption": [ + "HP:0006288" + ], + "advanced tooth eruption": [ + "HP:0006288" + ], + "early dental eruption": [ + "HP:0006288" + ], + "early eruption of teeth": [ + "HP:0006288" + ], + "eruption , advance": [ + "HP:0006288" + ], + "eruption , advanced": [ + "HP:0006288" + ], + "premature dental eruption": [ + "HP:0006288" + ], + "premature eruption of teeth": [ + "HP:0006288" + ], + "premature tooth eruption": [ + "HP:0006288" + ], + "agenesis of central incisor": [ + "HP:0006289" + ], + "absent central incisor": [ + "HP:0006289" + ], + "absent central incisors": [ + "HP:0006289" + ], + "failure of development of central incisor": [ + "HP:0006289" + ], + "miss central incisor": [ + "HP:0006289" + ], + "missing central incisors": [ + "HP:0006289" + ], + "discolored lateral incisor": [ + "HP:0006290" + ], + "discolored lateral incisors": [ + "HP:0006290" + ], + "abnormality of color of front teeth": [ + "HP:0006290" + ], + "abnormality of color of lateral incisor": [ + "HP:0006290" + ], + "abnormality of colour of front teeth": [ + "HP:0006290" + ], + "abnormality of colour of lateral incisor": [ + "HP:0006290" + ], + "abnormality of shade of lateral incisor": [ + "HP:0006290" + ], + "discolor front teeth": [ + "HP:0006290" + ], + "discolored front teeth": [ + "HP:0006290" + ], + "discolour front teeth": [ + "HP:0006290" + ], + "discoloured front teeth": [ + "HP:0006290" + ], + "discoloured lateral incisor": [ + "HP:0006290" + ], + "discoloured lateral incisors": [ + "HP:0006290" + ], + "mark delay in eruption of permanent teeth": [ + "HP:0006291" + ], + "marked delay in eruption of permanent teeth": [ + "HP:0006291" + ], + "severe delay of eruption of adult teeth": [ + "HP:0006291" + ], + "severe delay of eruption of permanent teeth": [ + "HP:0006291" + ], + "very late eruption of adult teeth": [ + "HP:0006291" + ], + "very late eruption of permanent teeth": [ + "HP:0006291" + ], + "abnormality of dental eruption": [ + "HP:0006292" + ], + "abnormal dental eruption": [ + "HP:0006292" + ], + "abnormality of tooth eruption": [ + "HP:0006292" + ], + "anomaly of dental eruption": [ + "HP:0006292" + ], + "anomaly of tooth eruption": [ + "HP:0006292" + ], + "disorder of dental eruption": [ + "HP:0006292" + ], + "disorder of tooth eruption": [ + "HP:0006292" + ], + "disturbance of dental eruption": [ + "HP:0006292" + ], + "disturbance of tooth eruption": [ + "HP:0006292" + ], + "agenesis of maxillary central incisor": [ + "HP:0006293" + ], + "absence of maxillary central incisor": [ + "HP:0006293" + ], + "failure of development of maxillary central incisor": [ + "HP:0006293" + ], + "miss maxillary central incisor": [ + "HP:0006293" + ], + "missing maxillary central incisor": [ + "HP:0006293" + ], + "miss upper central incisor": [ + "HP:0006293" + ], + "missing upper central incisor": [ + "HP:0006293" + ], + "enamel hypoplasia": [ + "HP:0006297" + ], + "defective enamel matrix": [ + "HP:0006297" + ], + "dental enamel hypoplasia": [ + "HP:0006297" + ], + "dysplasia of tooth enamel": [ + "HP:0006297" + ], + "enamel dysplasia": [ + "HP:0006297" + ], + "enamel hypotrophy": [ + "HP:0006297" + ], + "enamel , underdevelop": [ + "HP:0006297" + ], + "enamel , underdeveloped": [ + "HP:0006297" + ], + "hypoplasia of dental enamel": [ + "HP:0006297" + ], + "hypoplasia of tooth enamel": [ + "HP:0006297" + ], + "thin dental enamel": [ + "HP:0006297" + ], + "thin tooth enamel": [ + "HP:0006297" + ], + "underdeveloped teeth enamel": [ + "HP:0006297" + ], + "prolong bleeding after dental extraction": [ + "HP:0006298" + ], + "prolonged bleeding after dental extraction": [ + "HP:0006298" + ], + "dagger - shaped pulp calcification": [ + "HP:0006302" + ], + "dagger - shaped pulp calcifications": [ + "HP:0006302" + ], + "dagger shape pulp denticle": [ + "HP:0006302" + ], + "dagger shaped pulp denticles": [ + "HP:0006302" + ], + "dagger shape pulp stone": [ + "HP:0006302" + ], + "dagger shaped pulp stones": [ + "HP:0006302" + ], + "widely - space incisor": [ + "HP:0006304" + ], + "widely - spaced incisors": [ + "HP:0006304" + ], + "anterior diastema of teeth": [ + "HP:0006304" + ], + "diastema between front teeth": [ + "HP:0006304" + ], + "diastema between incisor": [ + "HP:0006304" + ], + "diastema between incisors": [ + "HP:0006304" + ], + "gap between front teeth": [ + "HP:0006304" + ], + "widely space front teeth": [ + "HP:0006304" + ], + "widely spaced front teeth": [ + "HP:0006304" + ], + "atrophy of alveolar ridge": [ + "HP:0006308" + ], + "atrophy of alveolar ridges": [ + "HP:0006308" + ], + "alveolar bone loss": [ + "HP:0006308" + ], + "atrophy of alveolar margin": [ + "HP:0006308" + ], + "atrophy of alveolar margins": [ + "HP:0006308" + ], + "atrophy of alveolar process of jaw": [ + "HP:0006308" + ], + "atrophy of alveolar processes of jaw": [ + "HP:0006308" + ], + "flattening of alveolar margin": [ + "HP:0006308" + ], + "flattening of alveolar process of jaw": [ + "HP:0006308" + ], + "flattening of alveolar processes of jaw": [ + "HP:0006308" + ], + "flattening of alveolar ridge": [ + "HP:0006308" + ], + "flattening of alveolar ridges": [ + "HP:0006308" + ], + "flattening of gum ridge": [ + "HP:0006308" + ], + "flattening of gum ridges": [ + "HP:0006308" + ], + "resorption of alveolar margin": [ + "HP:0006308" + ], + "resorption of alveolar margins": [ + "HP:0006308" + ], + "resorption of alveolar process of jaw": [ + "HP:0006308" + ], + "resorption of alveolar processes of jaw": [ + "HP:0006308" + ], + "resorption of alveolar ridge": [ + "HP:0006308" + ], + "resorption of alveolar ridges": [ + "HP:0006308" + ], + "shrinking of alveolar ridge": [ + "HP:0006308" + ], + "shrinking of alveolar ridges": [ + "HP:0006308" + ], + "shrinking of gum ridge": [ + "HP:0006308" + ], + "shrinking of gum ridges": [ + "HP:0006308" + ], + "generalize microdontia": [ + "HP:0006311" + ], + "generalized microdontia": [ + "HP:0006311" + ], + "decreased size of all teeth": [ + "HP:0006311" + ], + "decrease tooth mass": [ + "HP:0006311" + ], + "decreased tooth mass": [ + "HP:0006311" + ], + "decrease width of all teeth": [ + "HP:0006311" + ], + "decreased width of all teeth": [ + "HP:0006311" + ], + "generalise microdontia": [ + "HP:0006311" + ], + "generalised microdontia": [ + "HP:0006311" + ], + "hypotrophy of all teeth": [ + "HP:0006311" + ], + "tooth mass insufficiency": [ + "HP:0006311" + ], + "widely space primary teeth": [ + "HP:0006313" + ], + "widely spaced primary teeth": [ + "HP:0006313" + ], + "generalised spacing of primary teeth": [ + "HP:0006313" + ], + "generalize spacing of primary teeth": [ + "HP:0006313" + ], + "generalized spacing of primary teeth": [ + "HP:0006313" + ], + "wide gap between baby teeth": [ + "HP:0006313" + ], + "wide gaps between baby teeth": [ + "HP:0006313" + ], + "wide gap between primary teeth": [ + "HP:0006313" + ], + "wide gaps between primary teeth": [ + "HP:0006313" + ], + "widely space baby teeth": [ + "HP:0006313" + ], + "widely spaced baby teeth": [ + "HP:0006313" + ], + "widely space deciduous teeth": [ + "HP:0006313" + ], + "widely spaced deciduous teeth": [ + "HP:0006313" + ], + "widely space milk teeth": [ + "HP:0006313" + ], + "widely spaced milk teeth": [ + "HP:0006313" + ], + "solitary median maxillary central incisor": [ + "HP:0006315" + ], + "only one upper front tooth": [ + "HP:0006315" + ], + "single central incisor": [ + "HP:0006315" + ], + "single central upper incisor": [ + "HP:0006315" + ], + "single maxillary central incisor": [ + "HP:0006315" + ], + "single median incisor": [ + "HP:0006315" + ], + "single median maxillary central incisor": [ + "HP:0006315" + ], + "single median maxillary incisor": [ + "HP:0006315" + ], + "single midline maxillary incisor": [ + "HP:0006315" + ], + "single midline upper front tooth": [ + "HP:0006315" + ], + "solitary median maxillary central incisor syndrome": [ + "HP:0006315" + ], + "solitary midline maxillary central incisor": [ + "HP:0006315" + ], + "irregularly space teeth": [ + "HP:0006316" + ], + "irregularly spaced teeth": [ + "HP:0006316" + ], + "irregular dental spacing": [ + "HP:0006316" + ], + "variability of dental spacing": [ + "HP:0006316" + ], + "variability of space between teeth": [ + "HP:0006316" + ], + "variability of spacing between teeth": [ + "HP:0006316" + ], + "multiple non - erupt secondary teeth": [ + "HP:0006321" + ], + "multiple non - erupting secondary teeth": [ + "HP:0006321" + ], + "failure of eruption of multiple adult teeth": [ + "HP:0006321" + ], + "failure of eruption of multiple permanent teeth": [ + "HP:0006321" + ], + "multiple non - erupt adult teeth": [ + "HP:0006321" + ], + "multiple non - erupting adult teeth": [ + "HP:0006321" + ], + "multiple non - erupt permanent teeth": [ + "HP:0006321" + ], + "multiple non - erupting permanent teeth": [ + "HP:0006321" + ], + "multiple unerupted adult teeth": [ + "HP:0006321" + ], + "multiple unerupted permanent teeth": [ + "HP:0006321" + ], + "premature loss of primary teeth": [ + "HP:0006323" + ], + "early loss of baby teeth": [ + "HP:0006323" + ], + "early loss of deciduous teeth": [ + "HP:0006323" + ], + "early loss of primary teeth": [ + "HP:0006323" + ], + "premature deciduous tooth loss": [ + "HP:0006323" + ], + "premature exfoliation of deciduous teeth": [ + "HP:0006323" + ], + "premature exfoliation of primary teeth": [ + "HP:0006323" + ], + "premature loss of baby teeth": [ + "HP:0006323" + ], + "premature loss of deciduous teeth": [ + "HP:0006323" + ], + "bury teeth encase in mucopolysaccharide": [ + "HP:0006326" + ], + "buried teeth encased in mucopolysaccharide": [ + "HP:0006326" + ], + "failure of dental eruption due to mucopolysaccharidoses": [ + "HP:0006326" + ], + "failure of tooth eruption due to mucopolysaccharidoses": [ + "HP:0006326" + ], + "impact teeth due to mucopolysaccharidoses": [ + "HP:0006326" + ], + "impacted teeth due to mucopolysaccharidoses": [ + "HP:0006326" + ], + "unerupted dentition due to mucopolysaccharidoses": [ + "HP:0006326" + ], + "unerupted teeth due to mucopolysaccharidoses": [ + "HP:0006326" + ], + "alveolar process hypoplasia": [ + "HP:0006329" + ], + "decreased size of alveolar process of jaw": [ + "HP:0006329" + ], + "decreased size of alveolar ridge": [ + "HP:0006329" + ], + "deficiency of alveolar process of jaw": [ + "HP:0006329" + ], + "deficiency of alveolar ridge": [ + "HP:0006329" + ], + "hypoplasia of alveolar ridge": [ + "HP:0006329" + ], + "hypoplastic alveolar bone": [ + "HP:0006329" + ], + "hypotrophic alveolar process of jaw": [ + "HP:0006329" + ], + "hypotrophic alveolar ridge": [ + "HP:0006329" + ], + "small alveolar process of jaw": [ + "HP:0006329" + ], + "small alveolar ridge": [ + "HP:0006329" + ], + "underdevelopment of alveolar process of jaw": [ + "HP:0006329" + ], + "underdevelopment of alveolar ridge": [ + "HP:0006329" + ], + "rotate maxillary central incisor": [ + "HP:0006330" + ], + "rotated maxillary central incisors": [ + "HP:0006330" + ], + "rotate upper central incisor": [ + "HP:0006330" + ], + "rotated upper central incisors": [ + "HP:0006330" + ], + "rotate upper front teeth": [ + "HP:0006330" + ], + "rotated upper front teeth": [ + "HP:0006330" + ], + "turn upper front teeth": [ + "HP:0006330" + ], + "turned upper front teeth": [ + "HP:0006330" + ], + "twist upper front teeth": [ + "HP:0006330" + ], + "twisted upper front teeth": [ + "HP:0006330" + ], + "supernumerary maxillary incisor": [ + "HP:0006332" + ], + "extra upper front tooth": [ + "HP:0006332" + ], + "crowd maxillary incisor": [ + "HP:0006333" + ], + "crowded maxillary incisors": [ + "HP:0006333" + ], + "crowd upper front teeth": [ + "HP:0006333" + ], + "crowded upper front teeth": [ + "HP:0006333" + ], + "crowd upper incisor": [ + "HP:0006333" + ], + "crowded upper incisors": [ + "HP:0006333" + ], + "overlap maxillary incisor": [ + "HP:0006333" + ], + "overlapped maxillary incisors": [ + "HP:0006333" + ], + "overlap upper front teeth": [ + "HP:0006333" + ], + "overlapped upper front teeth": [ + "HP:0006333" + ], + "hypoplasia of the primary teeth": [ + "HP:0006334" + ], + "decreased size of baby teeth": [ + "HP:0006334" + ], + "decreased size of deciduous teeth": [ + "HP:0006334" + ], + "decreased size of milk teeth": [ + "HP:0006334" + ], + "decreased size of primary teeth": [ + "HP:0006334" + ], + "hypoplastic deciduous teeth": [ + "HP:0006334" + ], + "small baby teeth": [ + "HP:0006334" + ], + "small milk teeth": [ + "HP:0006334" + ], + "small primary teeth": [ + "HP:0006334" + ], + "underdevelopment of baby teeth": [ + "HP:0006334" + ], + "underdevelopment of milk teeth": [ + "HP:0006334" + ], + "underdevelopment of primary teeth": [ + "HP:0006334" + ], + "persistence of primary teeth": [ + "HP:0006335" + ], + "deciduous teeth retention": [ + "HP:0006335" + ], + "delayed loss of baby teeth": [ + "HP:0006335" + ], + "delayed loss of deciduous teeth": [ + "HP:0006335" + ], + "delayed loss of primary teeth": [ + "HP:0006335" + ], + "failure to exfoliate deciduous teeth": [ + "HP:0006335" + ], + "failure to exfoliate primary teeth": [ + "HP:0006335" + ], + "failure to lose baby teeth": [ + "HP:0006335" + ], + "persistence of deciduous teeth": [ + "HP:0006335" + ], + "persistent deciduous dentition": [ + "HP:0006335" + ], + "persistent primary dentition": [ + "HP:0006335" + ], + "persistent primary teeth": [ + "HP:0006335" + ], + "retain baby teeth": [ + "HP:0006335" + ], + "retained baby teeth": [ + "HP:0006335" + ], + "retain deciduous teeth": [ + "HP:0006335" + ], + "retained deciduous teeth": [ + "HP:0006335" + ], + "retain primary teeth": [ + "HP:0006335" + ], + "retained primary teeth": [ + "HP:0006335" + ], + "short dental root": [ + "HP:0006336" + ], + "decreased length of dental root": [ + "HP:0006336" + ], + "decreased length of dental roots": [ + "HP:0006336" + ], + "decreased length of tooth root": [ + "HP:0006336" + ], + "decreased length of tooth roots": [ + "HP:0006336" + ], + "dental root hypoplasia": [ + "HP:0006336" + ], + "dental root hypotrophy": [ + "HP:0006336" + ], + "rhizomicry": [ + "HP:0006336" + ], + "root dwarfism": [ + "HP:0006336" + ], + "short dental roots": [ + "HP:0006336" + ], + "short tooth root": [ + "HP:0006336" + ], + "short tooth roots": [ + "HP:0006336" + ], + "underdeveloped dental root": [ + "HP:0006336" + ], + "underdeveloped dental roots": [ + "HP:0006336" + ], + "underdeveloped tooth root": [ + "HP:0006336" + ], + "underdeveloped tooth roots": [ + "HP:0006336" + ], + "premature eruption of permanent teeth": [ + "HP:0006337" + ], + "early eruption of adult teeth": [ + "HP:0006337" + ], + "early eruption of permanent teeth": [ + "HP:0006337" + ], + "precocious eruption of secondary dentition": [ + "HP:0006337" + ], + "precocious eruption of secondary teeth": [ + "HP:0006337" + ], + "premature eruption of adult teeth": [ + "HP:0006337" + ], + "malformation of mandibular premolar": [ + "HP:0006338" + ], + "malformation of low premolar": [ + "HP:0006338" + ], + "malformation of lower premolar": [ + "HP:0006338" + ], + "malformation of mandibular bicuspid": [ + "HP:0006338" + ], + "conical mandibular incisor": [ + "HP:0006339" + ], + "cone shape low front tooth": [ + "HP:0006339" + ], + "cone shaped lower front tooth": [ + "HP:0006339" + ], + "conoid mandibular incisor": [ + "HP:0006339" + ], + "low front shark tooth": [ + "HP:0006339" + ], + "lower front shark tooth": [ + "HP:0006339" + ], + "peg shape low front tooth": [ + "HP:0006339" + ], + "peg shaped lower front tooth": [ + "HP:0006339" + ], + "peg shape mandibular incisor": [ + "HP:0006339" + ], + "peg shaped mandibular incisor": [ + "HP:0006339" + ], + "point mandibular incisor": [ + "HP:0006339" + ], + "pointed mandibular incisor": [ + "HP:0006339" + ], + "pointed mandibular incisors": [ + "HP:0006339" + ], + "peg - shaped maxillary lateral incisor": [ + "HP:0006342" + ], + "peg - shaped maxillary lateral incisors": [ + "HP:0006342" + ], + "cone shape upper lateral incisor": [ + "HP:0006342" + ], + "cone shaped upper lateral incisors": [ + "HP:0006342" + ], + "conical maxillary lateral incisor": [ + "HP:0006342" + ], + "conical maxillary lateral incisors": [ + "HP:0006342" + ], + "conoid upper lateral incisor": [ + "HP:0006342" + ], + "conoid upper lateral incisors": [ + "HP:0006342" + ], + "peg lateral": [ + "HP:0006342" + ], + "peg laterals": [ + "HP:0006342" + ], + "peg shape upper lateral incisor": [ + "HP:0006342" + ], + "peg shaped upper lateral incisors": [ + "HP:0006342" + ], + "peg - shape tooth": [ + "HP:0006342" + ], + "peg - shaped tooth": [ + "HP:0006342" + ], + "point upper lateral incisor": [ + "HP:0006342" + ], + "pointed upper lateral incisors": [ + "HP:0006342" + ], + "abnormality of primary molar morphology": [ + "HP:0006344" + ], + "abnormality of deciduous molar morphology": [ + "HP:0006344" + ], + "abnormality of shape of baby molar": [ + "HP:0006344" + ], + "abnormality of shape of primary molar": [ + "HP:0006344" + ], + "screwdriver - shaped incisor": [ + "HP:0006346" + ], + "screwdriver - shaped incisors": [ + "HP:0006346" + ], + "screwdriver shape front teeth": [ + "HP:0006346" + ], + "screwdriver shaped front teeth": [ + "HP:0006346" + ], + "microdontia of primary teeth": [ + "HP:0006347" + ], + "decreased size of primary tooth": [ + "HP:0006347" + ], + "decrease width of baby teeth": [ + "HP:0006347" + ], + "decreased width of baby teeth": [ + "HP:0006347" + ], + "decrease width of deciduous teeth": [ + "HP:0006347" + ], + "decreased width of deciduous teeth": [ + "HP:0006347" + ], + "decrease width of milk teeth": [ + "HP:0006347" + ], + "decreased width of milk teeth": [ + "HP:0006347" + ], + "decrease width of primary tooth": [ + "HP:0006347" + ], + "decreased width of primary tooth": [ + "HP:0006347" + ], + "microdontia of deciduous teeth": [ + "HP:0006347" + ], + "small deciduous teeth": [ + "HP:0006347" + ], + "agenesis of permanent teeth": [ + "HP:0006349" + ], + "absence of permanent teeth": [ + "HP:0006349" + ], + "absent permanent teeth": [ + "HP:0006349" + ], + "agenesis of permanent dentition": [ + "HP:0006349" + ], + "agenesis of secondary dentition": [ + "HP:0006349" + ], + "failure of development of permanent teeth": [ + "HP:0006349" + ], + "failure of development of secondary teeth": [ + "HP:0006349" + ], + "miss teeth": [ + "HP:0006349" + ], + "missing teeth": [ + "HP:0006349" + ], + "pulp obliteration": [ + "HP:0006350" + ], + "crescent / chevron - shaped pulp chamber": [ + "HP:0006350" + ], + "crescent / chevron - shaped pulp chambers": [ + "HP:0006350" + ], + "narrowing of pulp chamber of tooth": [ + "HP:0006350" + ], + "obliteration of the pulp chamber": [ + "HP:0006350" + ], + "pulp canal obliteration": [ + "HP:0006350" + ], + "reduce size of pulp chamber of tooth": [ + "HP:0006350" + ], + "reduced size of pulp chamber of tooth": [ + "HP:0006350" + ], + "small pulp chamber of tooth": [ + "HP:0006350" + ], + "failure of eruption of permanent teeth": [ + "HP:0006352" + ], + "failure of eruption of adult teeth": [ + "HP:0006352" + ], + "unerupted adult dentition": [ + "HP:0006352" + ], + "unerupted adult teeth": [ + "HP:0006352" + ], + "unerupted permanent dentition": [ + "HP:0006352" + ], + "unerupted permanent teeth": [ + "HP:0006352" + ], + "hypoplasia of the tooth germ": [ + "HP:0006353" + ], + "decreased size of tooth bud": [ + "HP:0006353" + ], + "decreased size of tooth germ": [ + "HP:0006353" + ], + "hypoplastic tooth bud": [ + "HP:0006353" + ], + "hypoplastic tooth buds": [ + "HP:0006353" + ], + "hypotrophic tooth germ": [ + "HP:0006353" + ], + "small tooth bud": [ + "HP:0006353" + ], + "small tooth germ": [ + "HP:0006353" + ], + "underdevelopment of tooth bud": [ + "HP:0006353" + ], + "underdevelopment of tooth germ": [ + "HP:0006353" + ], + "agenesis of mandibular central incisor": [ + "HP:0006355" + ], + "absence of low central incisor": [ + "HP:0006355" + ], + "absence of lower central incisor": [ + "HP:0006355" + ], + "absence of mandibular central incisor": [ + "HP:0006355" + ], + "failure of development of mandibular central incisor": [ + "HP:0006355" + ], + "miss low central incisor": [ + "HP:0006355" + ], + "missing lower central incisor": [ + "HP:0006355" + ], + "miss mandibular central incisor": [ + "HP:0006355" + ], + "missing mandibular central incisor": [ + "HP:0006355" + ], + "premature loss of permanent teeth": [ + "HP:0006357" + ], + "early loss of adult teeth": [ + "HP:0006357" + ], + "early loss of permanent teeth": [ + "HP:0006357" + ], + "early loss of secondary dentition": [ + "HP:0006357" + ], + "premature loss of adult teeth": [ + "HP:0006357" + ], + "premature loss of secondary teeth": [ + "HP:0006357" + ], + "shovel - shape maxillary central incisor": [ + "HP:0006358" + ], + "shovel - shaped maxillary central incisors": [ + "HP:0006358" + ], + "shovel tooth": [ + "HP:0006358" + ], + "shovel - shape upper front teeth": [ + "HP:0006358" + ], + "shovel - shaped upper front teeth": [ + "HP:0006358" + ], + "irregular femoral epiphysis": [ + "HP:0006361" + ], + "irregular thighbone end part": [ + "HP:0006361" + ], + "varus deformity of humeral neck": [ + "HP:0006362" + ], + "adductor longus contracture": [ + "HP:0006366" + ], + "adductor longus contractures": [ + "HP:0006366" + ], + "crumple long bone": [ + "HP:0006367" + ], + "crumpled long bones": [ + "HP:0006367" + ], + "forearm reduction defect": [ + "HP:0006368" + ], + "forearm reduction defects": [ + "HP:0006368" + ], + "irregular patella": [ + "HP:0006369" + ], + "irregular patellae": [ + "HP:0006369" + ], + "irregular patellar contour": [ + "HP:0006369" + ], + "irregular patellar margin": [ + "HP:0006369" + ], + "irregular patellar margins": [ + "HP:0006369" + ], + "distal ulnar epiphyseal stipple": [ + "HP:0006370" + ], + "distal ulnar epiphyseal stippling": [ + "HP:0006370" + ], + "distal ulnar epiphyseal calcification": [ + "HP:0006370" + ], + "distal ulnar epiphyseal calcifications": [ + "HP:0006370" + ], + "broad long bone diaphysis": [ + "HP:0006371" + ], + "broad long bone diaphyses": [ + "HP:0006371" + ], + "broad shaft of long bone": [ + "HP:0006371" + ], + "wide shaft of long bone": [ + "HP:0006371" + ], + "dumbbell - shape femur": [ + "HP:0006375" + ], + "dumbbell - shaped femur": [ + "HP:0006375" + ], + "dumbbell - shape thighbone": [ + "HP:0006375" + ], + "dumbbell - shaped thighbone": [ + "HP:0006375" + ], + "limited elbow flexion": [ + "HP:0006376" + ], + "osteolysis of patella": [ + "HP:0006378" + ], + "osteolysis of patellae": [ + "HP:0006378" + ], + "proximal tibial hypoplasia": [ + "HP:0006379" + ], + "proximal tibial hypopolasia": [ + "HP:0006379" + ], + "knee flexion contracture": [ + "HP:0006380" + ], + "contracture of knee": [ + "HP:0006380" + ], + "contractures of knees": [ + "HP:0006380" + ], + "contracture of the knee": [ + "HP:0006380" + ], + "contractures of the knees": [ + "HP:0006380" + ], + "flexion contracture of knee": [ + "HP:0006380" + ], + "flexion contracture of knees": [ + "HP:0006380" + ], + "flexion contracture at both knee": [ + "HP:0006380" + ], + "flexion contractures at both knees": [ + "HP:0006380" + ], + "flexion contractures of knees": [ + "HP:0006380" + ], + "flexion deformity of the knee": [ + "HP:0006380" + ], + "inability to straighten knee": [ + "HP:0006380" + ], + "knee contracture": [ + "HP:0006380" + ], + "knee contractures": [ + "HP:0006380" + ], + "knee flexion contractures": [ + "HP:0006380" + ], + "knee flexion deformity": [ + "HP:0006380" + ], + "rudimentary fibula": [ + "HP:0006381" + ], + "rudimentary to absent fibula": [ + "HP:0006381" + ], + "rudimentary to absent fibulae": [ + "HP:0006381" + ], + "small to absent calf bone": [ + "HP:0006381" + ], + "small to absent fibula": [ + "HP:0006381" + ], + "progressive bowing of long bone": [ + "HP:0006383" + ], + "progressive bowing of long bones": [ + "HP:0006383" + ], + "club - shaped distal femur": [ + "HP:0006384" + ], + "club - shaped distal femora": [ + "HP:0006384" + ], + "club - shape outermost end of thighbone": [ + "HP:0006384" + ], + "club - shaped outermost end of thighbone": [ + "HP:0006384" + ], + "short low limb": [ + "HP:0006385" + ], + "short lower limbs": [ + "HP:0006385" + ], + "short leg": [ + "HP:0006385" + ], + "short legs": [ + "HP:0006385" + ], + "hypoplastic distal radial epiphysis": [ + "HP:0006386" + ], + "hypoplastic distal radial epiphyses": [ + "HP:0006386" + ], + "wide distal femoral metaphysis": [ + "HP:0006387" + ], + "broad outermost wide portion of thighbone": [ + "HP:0006387" + ], + "wide distal metaphysis of femur": [ + "HP:0006387" + ], + "limited knee flexion": [ + "HP:0006389" + ], + "anterior tibial bowing": [ + "HP:0006390" + ], + "anterior bowing of tibia": [ + "HP:0006390" + ], + "overtubulated long bone": [ + "HP:0006391" + ], + "overtubulated long bones": [ + "HP:0006391" + ], + "increase density of long bone": [ + "HP:0006392" + ], + "increased density of long bones": [ + "HP:0006392" + ], + "limited pronation / supination of forearm": [ + "HP:0006394" + ], + "lateral displacement of patella": [ + "HP:0006397" + ], + "lateral displacement of patellae": [ + "HP:0006397" + ], + "flat distal femoral epiphysis": [ + "HP:0006398" + ], + "flat end part of outermost thighbone": [ + "HP:0006398" + ], + "flatten distal femoral epiphysis": [ + "HP:0006398" + ], + "flattened distal femoral epiphyses": [ + "HP:0006398" + ], + "absent knee epiphysis": [ + "HP:0006400" + ], + "absent knee epiphyses": [ + "HP:0006400" + ], + "absent knee end part": [ + "HP:0006400" + ], + "distal shortening of limb": [ + "HP:0006402" + ], + "distal shortening of limbs": [ + "HP:0006402" + ], + "short out part of limb": [ + "HP:0006402" + ], + "short outer part of limbs": [ + "HP:0006402" + ], + "club - shape proximal femur": [ + "HP:0006406" + ], + "club - shaped proximal femur": [ + "HP:0006406" + ], + "club - shape innermost end of thighbone": [ + "HP:0006406" + ], + "club - shaped innermost end of thighbone": [ + "HP:0006406" + ], + "irregular distal femoral epiphysis": [ + "HP:0006407" + ], + "irregular outermost thighbone end part": [ + "HP:0006407" + ], + "distal tapering femur": [ + "HP:0006408" + ], + "tapering of outermost end of thighbone": [ + "HP:0006408" + ], + "progressive leg bowing": [ + "HP:0006409" + ], + "broad tibial metaphyses": [ + "HP:0006413" + ], + "broad wide portion of shankbone": [ + "HP:0006413" + ], + "broad wide portion of shinbone": [ + "HP:0006413" + ], + "distal tibial bowing": [ + "HP:0006414" + ], + "bowing of the distal tibia": [ + "HP:0006414" + ], + "tibial bowing at ankle": [ + "HP:0006414" + ], + "cortically dense long tubular bone": [ + "HP:0006415" + ], + "cortically dense long tubular bones": [ + "HP:0006415" + ], + "broad femoral metaphyses": [ + "HP:0006417" + ], + "broad wide portion of thigh bone": [ + "HP:0006417" + ], + "asymmetric radial dysplasia": [ + "HP:0006420" + ], + "peg - like central prominence of distal tibial metaphyses": [ + "HP:0006423" + ], + "elongate radius": [ + "HP:0006424" + ], + "elongated radius": [ + "HP:0006424" + ], + "rudimentary to absent tibia": [ + "HP:0006426" + ], + "rudimentary to absent tibiae": [ + "HP:0006426" + ], + "broad femoral neck": [ + "HP:0006429" + ], + "broadening of femoral neck": [ + "HP:0006429" + ], + "wide femoral neck": [ + "HP:0006429" + ], + "wide neck of thigh bone": [ + "HP:0006429" + ], + "widen femoral neck": [ + "HP:0006429" + ], + "widened femoral necks": [ + "HP:0006429" + ], + "proximal femoral metaphyseal abnormality": [ + "HP:0006431" + ], + "abnormal wide portion of innermost thighbone": [ + "HP:0006431" + ], + "trapezoidal distal femoral condyle": [ + "HP:0006432" + ], + "trapezoidal distal femoral condyles": [ + "HP:0006432" + ], + "radial dysplasia": [ + "HP:0006433" + ], + "dysplastic radius": [ + "HP:0006433" + ], + "dysplastic radii": [ + "HP:0006433" + ], + "radial longitudinal deficiency": [ + "HP:0006433" + ], + "hypoplasia of proximal radius": [ + "HP:0006434" + ], + "proximal radial shortening": [ + "HP:0006434" + ], + "obsolete shortening of the tibia": [ + "HP:0006436" + ], + "disproportionate prominence of the femoral medial condyle": [ + "HP:0006437" + ], + "enlargement of the distal femoral epiphysis": [ + "HP:0006438" + ], + "enlargement of the outermost thighbone end part": [ + "HP:0006438" + ], + "large distal femoral epiphysis": [ + "HP:0006438" + ], + "large distal femoral epiphyses": [ + "HP:0006438" + ], + "radioulnar dislocation": [ + "HP:0006439" + ], + "dislocate radioulnar joint": [ + "HP:0006439" + ], + "dislocated radioulnar joints": [ + "HP:0006439" + ], + "increase density of long bone diaphysis": [ + "HP:0006440" + ], + "increased density of long bone diaphyses": [ + "HP:0006440" + ], + "increase density of shaft of long bone": [ + "HP:0006440" + ], + "increased density of shaft of long bone": [ + "HP:0006440" + ], + "lateral humeral condyle aplasia": [ + "HP:0006441" + ], + "hypoplasia of proximal fibula": [ + "HP:0006442" + ], + "small innermost upper end of calf bone": [ + "HP:0006442" + ], + "underdeveloped innermost upper end of calf bone": [ + "HP:0006442" + ], + "patellar aplasia": [ + "HP:0006443" + ], + "absent kneecap": [ + "HP:0006443" + ], + "absent patella": [ + "HP:0006443" + ], + "absent patellae": [ + "HP:0006443" + ], + "absent patellas": [ + "HP:0006443" + ], + "aplastic patella": [ + "HP:0006443" + ], + "aplastic patellae": [ + "HP:0006443" + ], + "dysplastic patella": [ + "HP:0006446" + ], + "distal radial epiphyseal osteolysis": [ + "HP:0006449" + ], + "multicentric ossification of proximal femoral epiphysis": [ + "HP:0006450" + ], + "multicentric ossification of proximal femoral epiphyses": [ + "HP:0006450" + ], + "lateral displacement of the femoral head": [ + "HP:0006453" + ], + "laterally displaced femoral head": [ + "HP:0006453" + ], + "laterally displaced femoral heads": [ + "HP:0006453" + ], + "delay patellar ossification": [ + "HP:0006454" + ], + "delayed patellar ossification": [ + "HP:0006454" + ], + "delay bone maturation of the knee cap": [ + "HP:0006454" + ], + "delayed bone maturation of the knee cap": [ + "HP:0006454" + ], + "delay patella ossification": [ + "HP:0006454" + ], + "delayed patellae ossification": [ + "HP:0006454" + ], + "irregular proximal tibial epiphysis": [ + "HP:0006456" + ], + "irregular proximal tibial epiphyses": [ + "HP:0006456" + ], + "irregular innermost shankbone end part": [ + "HP:0006456" + ], + "irregular innermost shinbone end part": [ + "HP:0006456" + ], + "dorsal subluxation of ulna": [ + "HP:0006459" + ], + "increase laxity of ankle": [ + "HP:0006460" + ], + "increased laxity of ankles": [ + "HP:0006460" + ], + "proximal femoral epiphysiolysis": [ + "HP:0006461" + ], + "slip capilal femoral epiphysis": [ + "HP:0006461" + ], + "slipped capilal femoral epiphysis": [ + "HP:0006461" + ], + "slipped capital femoral epiphysis": [ + "HP:0006461" + ], + "slipped capital femoral epiphyses": [ + "HP:0006461" + ], + "slipped end part of innermost thighbone": [ + "HP:0006461" + ], + "generalize bone demineralization": [ + "HP:0006462" + ], + "generalized bone demineralization": [ + "HP:0006462" + ], + "generalise bone demineralization": [ + "HP:0006462" + ], + "generalised bone demineralization": [ + "HP:0006462" + ], + "rickets of the low limb": [ + "HP:0006463" + ], + "rickets of the lower limbs": [ + "HP:0006463" + ], + "periosteal thickening of long tubular bone": [ + "HP:0006465" + ], + "periosteal thickening of long tubular bones": [ + "HP:0006465" + ], + "ankle flexion contracture": [ + "HP:0006466" + ], + "ankle contracture": [ + "HP:0006466" + ], + "ankle contractures": [ + "HP:0006466" + ], + "contracture of the ankle": [ + "HP:0006466" + ], + "contractures of the ankles": [ + "HP:0006466" + ], + "limited shoulder movement": [ + "HP:0006467" + ], + "thin long bone diaphysis": [ + "HP:0006470" + ], + "thin long bone diaphyses": [ + "HP:0006470" + ], + "thin diaphysis of long bone": [ + "HP:0006470" + ], + "thin diaphyses of long bones": [ + "HP:0006470" + ], + "thin shaft of long bone": [ + "HP:0006470" + ], + "fix elbow flexion": [ + "HP:0006471" + ], + "fixed elbow flexion": [ + "HP:0006471" + ], + "anterior bowing of long bone": [ + "HP:0006473" + ], + "anterior bowing of long bones": [ + "HP:0006473" + ], + "abnormality of the pancreatic islet cell": [ + "HP:0006476" + ], + "abnormality of the pancreatic islet cells": [ + "HP:0006476" + ], + "abnormality of the alveolar ridge": [ + "HP:0006477" + ], + "abnormality of the alveolar ridges": [ + "HP:0006477" + ], + "abnormality of alveolar margin": [ + "HP:0006477" + ], + "abnormality of alveolar process of jaw": [ + "HP:0006477" + ], + "abnormality of alveolar processes of jaw": [ + "HP:0006477" + ], + "abnormality of dentoalveolar ridge": [ + "HP:0006477" + ], + "abnormality of dentoalveolar ridges": [ + "HP:0006477" + ], + "abnormality of gum ridge": [ + "HP:0006477" + ], + "defect in alveolar ridge": [ + "HP:0006477" + ], + "abnormal dental pulp morphology": [ + "HP:0006479" + ], + "abnormality of the dental pulp": [ + "HP:0006479" + ], + "abnormality of tooth pulp": [ + "HP:0006479" + ], + "endodontic abnormality": [ + "HP:0006479" + ], + "premature loss of teeth": [ + "HP:0006480" + ], + "early tooth loss": [ + "HP:0006480" + ], + "loss of teeth": [ + "HP:0006480" + ], + "premature exfoliation of teeth": [ + "HP:0006480" + ], + "premature teeth loss": [ + "HP:0006480" + ], + "premature tooth loss": [ + "HP:0006480" + ], + "abnormality of primary teeth": [ + "HP:0006481" + ], + "abnormality of baby teeth": [ + "HP:0006481" + ], + "abnormality of deciduous teeth": [ + "HP:0006481" + ], + "abnormality of milk teeth": [ + "HP:0006481" + ], + "abnormality of dental morphology": [ + "HP:0006482" + ], + "abnormality of dental shape": [ + "HP:0006482" + ], + "abnormality of shape of tooth": [ + "HP:0006482" + ], + "abnormally shape teeth": [ + "HP:0006482" + ], + "abnormally shaped teeth": [ + "HP:0006482" + ], + "deformity of teeth": [ + "HP:0006482" + ], + "dental deformity": [ + "HP:0006482" + ], + "dental malformation": [ + "HP:0006482" + ], + "dental malformations": [ + "HP:0006482" + ], + "malformation of teeth": [ + "HP:0006482" + ], + "malformed teeth": [ + "HP:0006482" + ], + "misshapen teeth": [ + "HP:0006482" + ], + "misshapened teeth": [ + "HP:0006482" + ], + "abnormal number of teeth": [ + "HP:0006483" + ], + "abnormal complement of teeth": [ + "HP:0006483" + ], + "abnormal tooth count": [ + "HP:0006483" + ], + "agenesis of incisor": [ + "HP:0006485" + ], + "absence of front tooth": [ + "HP:0006485" + ], + "absence of incisor": [ + "HP:0006485" + ], + "absence of incisors": [ + "HP:0006485" + ], + "failure of development of incisor": [ + "HP:0006485" + ], + "miss front tooth": [ + "HP:0006485" + ], + "missing front tooth": [ + "HP:0006485" + ], + "miss incisor": [ + "HP:0006485" + ], + "missing incisors": [ + "HP:0006485" + ], + "abnormal dental root morphology": [ + "HP:0006486" + ], + "abnormality of the dental root": [ + "HP:0006486" + ], + "abnormality of tooth root": [ + "HP:0006486" + ], + "dental root anomaly": [ + "HP:0006486" + ], + "bowing of the long bone": [ + "HP:0006487" + ], + "bowing of the long bones": [ + "HP:0006487" + ], + "bow long bone": [ + "HP:0006487" + ], + "bowed long bones": [ + "HP:0006487" + ], + "bowing of long bone": [ + "HP:0006487" + ], + "bowing of long bones": [ + "HP:0006487" + ], + "camptomelia": [ + "HP:0006487" + ], + "diaphyseal bowing": [ + "HP:0006487" + ], + "diaphyseal bowing of long bone": [ + "HP:0006487" + ], + "diaphyseal bowing of long bones": [ + "HP:0006487" + ], + "bowing of the arm": [ + "HP:0006488" + ], + "bending of the arm": [ + "HP:0006488" + ], + "abnormality of the femoral metaphysis": [ + "HP:0006489" + ], + "abnormality of the wide portion of the femoral bone": [ + "HP:0006489" + ], + "abnormality of low - limb metaphyses": [ + "HP:0006490" + ], + "abnormality of lower - limb metaphyses": [ + "HP:0006490" + ], + "abnormality of the wide portion of the low - limb bone": [ + "HP:0006490" + ], + "abnormality of the wide portion of the lower - limb bone": [ + "HP:0006490" + ], + "abnormality of the tibial metaphysis": [ + "HP:0006491" + ], + "abnormality of the wide portion of shankbone": [ + "HP:0006491" + ], + "abnormality of the wide portion of shinbone": [ + "HP:0006491" + ], + "aplasia / hypoplasia of the fibula": [ + "HP:0006492" + ], + "absent / small calf bone": [ + "HP:0006492" + ], + "absent / underdevelop calf bone": [ + "HP:0006492" + ], + "absent / underdeveloped calf bone": [ + "HP:0006492" + ], + "fibular aplasia / hypoplasia": [ + "HP:0006492" + ], + "hypoplastic / aplastic fibula": [ + "HP:0006492" + ], + "hypoplastic / aplastic fibulae": [ + "HP:0006492" + ], + "aplasia / hypoplasia involve bone of the low limb": [ + "HP:0006493" + ], + "aplasia / hypoplasia involving bones of the lower limbs": [ + "HP:0006493" + ], + "absent / small low limb bone": [ + "HP:0006493" + ], + "absent / small lower limb bones": [ + "HP:0006493" + ], + "absent / underdevelop low limb bone": [ + "HP:0006493" + ], + "absent / underdeveloped lower limb bones": [ + "HP:0006493" + ], + "aplasia / hypoplasia involve bone of the foot": [ + "HP:0006494" + ], + "aplasia / hypoplasia involving bones of the feet": [ + "HP:0006494" + ], + "absent / small foot bone": [ + "HP:0006494" + ], + "absent / small foot bones": [ + "HP:0006494" + ], + "absent / underdeveloped foot bone": [ + "HP:0006494" + ], + "absent / underdeveloped foot bones": [ + "HP:0006494" + ], + "aplasia / hypoplasia of the ulna": [ + "HP:0006495" + ], + "absence / underdevelopment of inner forearm bone": [ + "HP:0006495" + ], + "absent - hypoplastic ulna": [ + "HP:0006495" + ], + "absent - hypoplastic ulnae": [ + "HP:0006495" + ], + "absent / small ulna": [ + "HP:0006495" + ], + "hypoplasia or unilateral / bilateral absence of ulna": [ + "HP:0006495" + ], + "ulnar hypoplasia / aplasia": [ + "HP:0006495" + ], + "aplasia / hypoplasia involve bone of the upper limb": [ + "HP:0006496" + ], + "aplasia / hypoplasia involving bones of the upper limbs": [ + "HP:0006496" + ], + "absent / small bone of the upper limb": [ + "HP:0006496" + ], + "absent / small bones of the upper limbs": [ + "HP:0006496" + ], + "absent / underdeveloped bone of the upper limb": [ + "HP:0006496" + ], + "absent / underdeveloped bones of the upper limbs": [ + "HP:0006496" + ], + "aplasia / hypoplasia of the patella": [ + "HP:0006498" + ], + "absent or hypoplastic patella": [ + "HP:0006498" + ], + "absent or hypoplastic patellae": [ + "HP:0006498" + ], + "absent / hypoplastic patella": [ + "HP:0006498" + ], + "absent / small kneecap": [ + "HP:0006498" + ], + "absent / underdevelop kneecap": [ + "HP:0006498" + ], + "absent / underdeveloped kneecap": [ + "HP:0006498" + ], + "aplastic or hypoplastic patella": [ + "HP:0006498" + ], + "aplastic or hypoplastic patellae": [ + "HP:0006498" + ], + "hypoplastic or absent patella": [ + "HP:0006498" + ], + "patellar aplasia / hypoplasia": [ + "HP:0006498" + ], + "small to absent patella": [ + "HP:0006498" + ], + "small to absent patellae": [ + "HP:0006498" + ], + "abnormality of femoral epiphysis": [ + "HP:0006499" + ], + "abnormality of thighbone end part": [ + "HP:0006499" + ], + "abnormality of low limb epiphysis morphology": [ + "HP:0006500" + ], + "abnormality of lower limb epiphysis morphology": [ + "HP:0006500" + ], + "abnormal shape of end part of low limb end bone": [ + "HP:0006500" + ], + "abnormal shape of end part of lower limb end bone": [ + "HP:0006500" + ], + "abnormality involve the epiphysis of the low limb": [ + "HP:0006500" + ], + "abnormality involving the epiphyses of the lower limbs": [ + "HP:0006500" + ], + "aplasia / hypoplasia of the radius": [ + "HP:0006501" + ], + "absence or underdevelopment of the radius bone of the arm": [ + "HP:0006501" + ], + "absent / small radius": [ + "HP:0006501" + ], + "absent / underdevelop radius": [ + "HP:0006501" + ], + "absent / underdeveloped radius": [ + "HP:0006501" + ], + "radial aplasia / hypoplasia": [ + "HP:0006501" + ], + "aplasia / hypoplasia involve the carpal bone": [ + "HP:0006502" + ], + "aplasia / hypoplasia involving the carpal bones": [ + "HP:0006502" + ], + "absent / small wrist bone": [ + "HP:0006502" + ], + "absent / small wrist bones": [ + "HP:0006502" + ], + "absent / underdeveloped wrist bone": [ + "HP:0006502" + ], + "absent / underdeveloped wrist bones": [ + "HP:0006502" + ], + "aplasia / hypoplasia involve forearm bone": [ + "HP:0006503" + ], + "aplasia / hypoplasia involving forearm bones": [ + "HP:0006503" + ], + "absent / small forearm bone": [ + "HP:0006503" + ], + "absent / small forearm bones": [ + "HP:0006503" + ], + "absent / underdevelop forearm bone": [ + "HP:0006503" + ], + "absent / underdeveloped forearm bones": [ + "HP:0006503" + ], + "obsolete anomaly of the limb diaphyses morphology": [ + "HP:0006504" + ], + "abnormality of limb epiphysis morphology": [ + "HP:0006505" + ], + "abnormal shape of end part of limb bone": [ + "HP:0006505" + ], + "abnormal shape of end part of limb bones": [ + "HP:0006505" + ], + "abnormality involve the epiphysis of the limb": [ + "HP:0006505" + ], + "abnormality involving the epiphyses of the limbs": [ + "HP:0006505" + ], + "aplasia / hypoplasia of the humerus": [ + "HP:0006507" + ], + "absent / small long bone in upper arm": [ + "HP:0006507" + ], + "absent / underdevelop long bone in upper arm": [ + "HP:0006507" + ], + "absent / underdeveloped long bone in upper arm": [ + "HP:0006507" + ], + "abnormality of tibial epiphysis": [ + "HP:0006508" + ], + "abnormality of tibial epiphyses": [ + "HP:0006508" + ], + "abnormality of end part of shinbone": [ + "HP:0006508" + ], + "diverticulosis of trachea": [ + "HP:0006509" + ], + "paratracheal air cyst": [ + "HP:0006509" + ], + "tracheal diverticulosis": [ + "HP:0006509" + ], + "tracheal diverticulum": [ + "HP:0006509" + ], + "tracheocele": [ + "HP:0006509" + ], + "chronic pulmonary obstruction": [ + "HP:0006510" + ], + "chronic obstructive pulmonary disease": [ + "HP:0006510" + ], + "laryngeal stridor": [ + "HP:0006511" + ], + "laryngeal stidor": [ + "HP:0006511" + ], + "intraalveolar nodular calcification": [ + "HP:0006514" + ], + "intraalveolar nodular calcifications": [ + "HP:0006514" + ], + "interstitial pneumonitis": [ + "HP:0006515" + ], + "hypersensitivity pneumonitis": [ + "HP:0006516" + ], + "intraalveolar phospholipid accumulation": [ + "HP:0006517" + ], + "alveolar proteinosis": [ + "HP:0006517" + ], + "detection of pas - positive extracellular material in broncho - alveolar lavage": [ + "HP:0006517" + ], + "pulmonary alveolar proteinosis": [ + "HP:0006517" + ], + "pulmonary venous occlusion": [ + "HP:0006518" + ], + "pulmonary venoocclusive disease": [ + "HP:0006518" + ], + "pulmonary venous stenosis": [ + "HP:0006518" + ], + "alveolar cell carcinoma": [ + "HP:0006519" + ], + "progressive pulmonary function impairment": [ + "HP:0006520" + ], + "pulmonary lymphangiectasia": [ + "HP:0006521" + ], + "pulmonary lymphangiectasis": [ + "HP:0006521" + ], + "repeat pneumothoraces": [ + "HP:0006522" + ], + "repeated pneumothoraces": [ + "HP:0006522" + ], + "repeat pneumothorax": [ + "HP:0006522" + ], + "repeated pneumothorax": [ + "HP:0006522" + ], + "tracheobronchial leiomyomatosis": [ + "HP:0006524" + ], + "obsolete lung segmentation defect": [ + "HP:0006525" + ], + "obsolete lung segmentation defects": [ + "HP:0006525" + ], + "lymphocytic interstitial pneumonia": [ + "HP:0006527" + ], + "lymphocytic interstitial pneumonitis": [ + "HP:0006527" + ], + "lymphoid interstitial pneumonia": [ + "HP:0006527" + ], + "lymphoid interstitial pneumonitis": [ + "HP:0006527" + ], + "chronic lung disease": [ + "HP:0006528" + ], + "abnormal pulmonary lymphatics": [ + "HP:0006529" + ], + "abnormal pulmonary interstitial morphology": [ + "HP:0006530" + ], + "abnormal lung parenchyma morphology": [ + "HP:0006530" + ], + "abnormality in area between air sac in lung": [ + "HP:0006530" + ], + "abnormality in area between air sacs in lung": [ + "HP:0006530" + ], + "interstitial lung disease": [ + "HP:0006530" + ], + "interstitial pulmonary disease": [ + "HP:0006530" + ], + "pleural lymphangiectasia": [ + "HP:0006531" + ], + "recurrent pneumonia": [ + "HP:0006532" + ], + "multiple pulmonary infection": [ + "HP:0006532" + ], + "multiple pulmonary infections": [ + "HP:0006532" + ], + "pneumonia , recurrent": [ + "HP:0006532" + ], + "pneumonia , recurrent episode": [ + "HP:0006532" + ], + "pneumonia , recurrent episodes": [ + "HP:0006532" + ], + "pulmonary infection": [ + "HP:0006532" + ], + "pulmonary infections": [ + "HP:0006532" + ], + "pulmonary infection , recurrent": [ + "HP:0006532" + ], + "pulmonary infections , recurrent": [ + "HP:0006532" + ], + "recurrent pulmonary infection": [ + "HP:0006532" + ], + "recurrent pulmonary infections": [ + "HP:0006532" + ], + "bronchodysplasia": [ + "HP:0006533" + ], + "recurrent intrapulmonary hemorrhage": [ + "HP:0006535" + ], + "recurrent bleed into lung": [ + "HP:0006535" + ], + "recurrent bleeding into lungs": [ + "HP:0006535" + ], + "recurrent intrapulmonary haemorrhage": [ + "HP:0006535" + ], + "recurrent pulmonary haemorrhage": [ + "HP:0006535" + ], + "recurrent pulmonary hemorrhage": [ + "HP:0006535" + ], + "airway obstruction": [ + "HP:0006536" + ], + "obstructive lung disease": [ + "HP:0006536" + ], + "pulmonary obstruction": [ + "HP:0006536" + ], + "recurrent bronchopulmonary infection": [ + "HP:0006538" + ], + "recurrent bronchopulmonary infections": [ + "HP:0006538" + ], + "recurrent infection in bronchus and lung": [ + "HP:0006538" + ], + "recurrent infections in bronchi and lungs": [ + "HP:0006538" + ], + "bronchial cartilage hypoplasia": [ + "HP:0006539" + ], + "underdevelopment of the bronical cartilage": [ + "HP:0006539" + ], + "obsolete chronic obstructive airway disease from birth": [ + "HP:0006541" + ], + "cardiorespiratory arrest": [ + "HP:0006543" + ], + "extrapulmonary sequestrum": [ + "HP:0006544" + ], + "diaphragmatic sequestrum": [ + "HP:0006544" + ], + "pulmonary arteriovenous malformation": [ + "HP:0006548" + ], + "pulmonary av malformation": [ + "HP:0006548" + ], + "unilateral primary pulmonary dysgenesis": [ + "HP:0006549" + ], + "primary pulmonary dysgenesis , unilateral": [ + "HP:0006549" + ], + "fibrocystic lung disease": [ + "HP:0006552" + ], + "acute hepatic failure": [ + "HP:0006554" + ], + "acute liver failure": [ + "HP:0006554" + ], + "diffuse hepatic steatosis": [ + "HP:0006555" + ], + "hepatic steatosis , diffuse": [ + "HP:0006555" + ], + "polycystic liver disease": [ + "HP:0006557" + ], + "decreased mitochondrial complex iii activity in liver tissue": [ + "HP:0006558" + ], + "hepatic calcification": [ + "HP:0006559" + ], + "liver calcification": [ + "HP:0006559" + ], + "liver calcifications": [ + "HP:0006559" + ], + "biliary hyperplasia": [ + "HP:0006560" + ], + "bile duct hyperplasia": [ + "HP:0006560" + ], + "lipid accumulation in hepatocytes": [ + "HP:0006561" + ], + "viral hepatitis": [ + "HP:0006562" + ], + "malformation of the hepatic ductal plate": [ + "HP:0006563" + ], + "fluctuate hepatomegaly": [ + "HP:0006564" + ], + "fluctuating hepatomegaly": [ + "HP:0006564" + ], + "increase hepatocellular lipid droplet": [ + "HP:0006565" + ], + "increased hepatocellular lipid droplets": [ + "HP:0006565" + ], + "neonatal cholestatic liver disease": [ + "HP:0006566" + ], + "increase hepatic glycogen content": [ + "HP:0006568" + ], + "increased hepatic glycogen content": [ + "HP:0006568" + ], + "increase liver glycogen content": [ + "HP:0006568" + ], + "increased liver glycogen content": [ + "HP:0006568" + ], + "reduced number of intrahepatic bile duct": [ + "HP:0006571" + ], + "reduced number of intrahepatic bile ducts": [ + "HP:0006571" + ], + "hepatic ductopenia": [ + "HP:0006571" + ], + "intrahepatic duct deficiency": [ + "HP:0006571" + ], + "subacute progressive viral hepatitis": [ + "HP:0006572" + ], + "acute hepatic steatosis": [ + "HP:0006573" + ], + "acute fatty liver": [ + "HP:0006573" + ], + "hepatic arteriovenous malformation": [ + "HP:0006574" + ], + "liver arteriovenous malformation": [ + "HP:0006574" + ], + "intrahepatic cholestasis with episodic jaundice": [ + "HP:0006575" + ], + "hepatic vascular malformation": [ + "HP:0006576" + ], + "hepatic vascular malformations": [ + "HP:0006576" + ], + "liver vascular malformation": [ + "HP:0006576" + ], + "liver vascular malformations": [ + "HP:0006576" + ], + "macronodular cirrhosis": [ + "HP:0006577" + ], + "prolonged neonatal jaundice": [ + "HP:0006579" + ], + "jaundice , neonatal": [ + "HP:0006579" + ], + "neonatal jaundice": [ + "HP:0006579" + ], + "prolonged yellowing of skin in newborn": [ + "HP:0006579" + ], + "portal fibrosis": [ + "HP:0006580" + ], + "portal fibrosis show on biopsy": [ + "HP:0006580" + ], + "portal fibrosis shown on biopsy": [ + "HP:0006580" + ], + "depletion of mitochondrial dna in liver": [ + "HP:0006581" + ], + "reye syndrome - like episode": [ + "HP:0006582" + ], + "reye syndrome - like episodes": [ + "HP:0006582" + ], + "fatal liver failure in infancy": [ + "HP:0006583" + ], + "small abnormally form scapula": [ + "HP:0006584" + ], + "small abnormally formed scapulae": [ + "HP:0006584" + ], + "small abnormally formed scapula": [ + "HP:0006584" + ], + "small abnormally form shoulder blade": [ + "HP:0006584" + ], + "small abnormally formed shoulder blade": [ + "HP:0006584" + ], + "congenital pseudoarthrosis of the clavicle": [ + "HP:0006585" + ], + "bipartite clavicle": [ + "HP:0006585" + ], + "clavicle pseudoarthrosis": [ + "HP:0006585" + ], + "pseudoarthrosis of clavicle": [ + "HP:0006585" + ], + "straight clavicle": [ + "HP:0006587" + ], + "straight clavicles": [ + "HP:0006587" + ], + "straight collarbone": [ + "HP:0006587" + ], + "flaring of low rib cage": [ + "HP:0006589" + ], + "flaring of lower rib cage": [ + "HP:0006589" + ], + "premature sternal synostosis": [ + "HP:0006590" + ], + "prematurely close sternal suture": [ + "HP:0006590" + ], + "prematurely closed sternal sutures": [ + "HP:0006590" + ], + "absent glenoid fossa": [ + "HP:0006591" + ], + "aplasia of the glenoid fossa": [ + "HP:0006591" + ], + "anomalous rib insertion to vertebrae": [ + "HP:0006593" + ], + "scapulohumeral synostosis": [ + "HP:0006595" + ], + "fusion of shoulder blade to long bone in upper arm": [ + "HP:0006595" + ], + "humero - scapulo synostosis": [ + "HP:0006595" + ], + "humeroscapular synostosis": [ + "HP:0006595" + ], + "synostosis of shoulder joint": [ + "HP:0006595" + ], + "restrict chest movement": [ + "HP:0006596" + ], + "restricted chest movement": [ + "HP:0006596" + ], + "diaphragmatic paralysis": [ + "HP:0006597" + ], + "paralyse diaphragm": [ + "HP:0006597" + ], + "paralysed diaphragm": [ + "HP:0006597" + ], + "paralyze diaphragm": [ + "HP:0006597" + ], + "paralyzed diaphragm": [ + "HP:0006597" + ], + "irregular ossification at anterior rib end": [ + "HP:0006598" + ], + "irregular ossification at anterior rib ends": [ + "HP:0006598" + ], + "medial widening of clavicle": [ + "HP:0006599" + ], + "medial widening of clavicles": [ + "HP:0006599" + ], + "progressive calcification of costochondral cartilage": [ + "HP:0006600" + ], + "flare , irregular rib end": [ + "HP:0006603" + ], + "flared , irregular rib ends": [ + "HP:0006603" + ], + "irregular chondrocostal junction": [ + "HP:0006606" + ], + "irregular chondrocostal junctions": [ + "HP:0006606" + ], + "irregular costochondral margin": [ + "HP:0006606" + ], + "irregular costochondral margins": [ + "HP:0006606" + ], + "precocious costochondral ossification": [ + "HP:0006607" + ], + "midclavicular hypoplasia": [ + "HP:0006608" + ], + "underdeveloped middle portion of the collarbone": [ + "HP:0006608" + ], + "wide intermamillary distance": [ + "HP:0006610" + ], + "wide - space nipple": [ + "HP:0006610" + ], + "wide - spaced nipples": [ + "HP:0006610" + ], + "widely space nipple": [ + "HP:0006610" + ], + "widely spaced nipples": [ + "HP:0006610" + ], + "widely - space nipple": [ + "HP:0006610" + ], + "widely - spaced nipples": [ + "HP:0006610" + ], + "decreased number of sternal ossification center": [ + "HP:0006611" + ], + "decreased number of sternal ossification centers": [ + "HP:0006611" + ], + "decreased number of sternal ossification centre": [ + "HP:0006611" + ], + "decreased number of sternal ossification centres": [ + "HP:0006611" + ], + "absent in utero rib ossification": [ + "HP:0006615" + ], + "absent rib calcification in utero": [ + "HP:0006615" + ], + "anterior rib punctate calcification": [ + "HP:0006619" + ], + "anterior rib punctate calcifications": [ + "HP:0006619" + ], + "costochondral joint sclerosis": [ + "HP:0006623" + ], + "sclerotic costochondral joint": [ + "HP:0006623" + ], + "sclerotic costochondral joints": [ + "HP:0006623" + ], + "multifocal breast carcinoma": [ + "HP:0006625" + ], + "multifocal breast cancer": [ + "HP:0006625" + ], + "absent sternal ossification": [ + "HP:0006628" + ], + "absent bone maturation in sternum": [ + "HP:0006628" + ], + "absent sternal mineralization": [ + "HP:0006628" + ], + "lack of sternal ossification": [ + "HP:0006628" + ], + "hypoplastic distal segment of scapula": [ + "HP:0006631" + ], + "hypoplastic distal segments of scapulae": [ + "HP:0006631" + ], + "small distal segment of the shoulder blade": [ + "HP:0006631" + ], + "small distal segments of the shoulder blade": [ + "HP:0006631" + ], + "small outermost segment of shoulder blade": [ + "HP:0006631" + ], + "small outermost segments of shoulder blade": [ + "HP:0006631" + ], + "underdeveloped outermost segment of shoulder blade": [ + "HP:0006631" + ], + "underdeveloped outermost segments of shoulder blade": [ + "HP:0006631" + ], + "glenoid fossa hypoplasia": [ + "HP:0006633" + ], + "glenoid hypoplasia": [ + "HP:0006633" + ], + "hypoplastic glenoid fossa": [ + "HP:0006633" + ], + "osteosclerosis of rib": [ + "HP:0006634" + ], + "osteosclerosis of ribs": [ + "HP:0006634" + ], + "increase bone density in rib": [ + "HP:0006634" + ], + "increased bone density in ribs": [ + "HP:0006634" + ], + "sternal punctate calcification": [ + "HP:0006637" + ], + "sternal punctate calcifications": [ + "HP:0006637" + ], + "midclavicular aplasia": [ + "HP:0006638" + ], + "miss middle part of collarbone": [ + "HP:0006638" + ], + "missing middle part of collarbone": [ + "HP:0006638" + ], + "multiple rib fracture": [ + "HP:0006640" + ], + "multiple rib fractures": [ + "HP:0006640" + ], + "prominent float rib": [ + "HP:0006641" + ], + "prominent floating ribs": [ + "HP:0006641" + ], + "large sternal ossification center": [ + "HP:0006642" + ], + "large sternal ossification centers": [ + "HP:0006642" + ], + "large sternal ossification centre": [ + "HP:0006642" + ], + "large sternal ossification centres": [ + "HP:0006642" + ], + "fuse sternal ossification center": [ + "HP:0006643" + ], + "fused sternal ossification centers": [ + "HP:0006643" + ], + "fuse sternal ossification centre": [ + "HP:0006643" + ], + "fused sternal ossification centres": [ + "HP:0006643" + ], + "thoracic dysplasia": [ + "HP:0006644" + ], + "thin clavicle": [ + "HP:0006645" + ], + "thin clavicles": [ + "HP:0006645" + ], + "thin collarbone": [ + "HP:0006645" + ], + "costal cartilage calcification": [ + "HP:0006646" + ], + "cartilaginous ossification of rib": [ + "HP:0006646" + ], + "congenital microthorax": [ + "HP:0006647" + ], + "costochondral pain": [ + "HP:0006649" + ], + "costochondral junction pain": [ + "HP:0006649" + ], + "thickening of the lateral border of the scapula": [ + "HP:0006650" + ], + "thickening of the lateral border of the shoulder blade": [ + "HP:0006650" + ], + "rib segmentation abnormality": [ + "HP:0006655" + ], + "rib segmentation abnormalities": [ + "HP:0006655" + ], + "hypoplasia of first rib": [ + "HP:0006657" + ], + "hypoplasia of first ribs": [ + "HP:0006657" + ], + "hypoplastic first rib": [ + "HP:0006657" + ], + "hypoplastic first ribs": [ + "HP:0006657" + ], + "small first rib": [ + "HP:0006657" + ], + "underdeveloped first rib": [ + "HP:0006657" + ], + "internally rotate shoulder": [ + "HP:0006659" + ], + "internally rotated shoulders": [ + "HP:0006659" + ], + "aplastic clavicle": [ + "HP:0006660" + ], + "absent clavicle": [ + "HP:0006660" + ], + "absent clavicles": [ + "HP:0006660" + ], + "absent collarbone": [ + "HP:0006660" + ], + "aplastic clavicles": [ + "HP:0006660" + ], + "coat hanger sign of rib": [ + "HP:0006665" + ], + "coat hanger sign of ribs": [ + "HP:0006665" + ], + "twelfth rib hypoplasia": [ + "HP:0006668" + ], + "small twelfth rib": [ + "HP:0006668" + ], + "underdeveloped twelfth rib": [ + "HP:0006668" + ], + "impaired myocardial contractility": [ + "HP:0006670" + ], + "paroxysmal atrial tachycardia": [ + "HP:0006671" + ], + "reduce systolic function": [ + "HP:0006673" + ], + "reduced systolic function": [ + "HP:0006673" + ], + "prolonged qrs complex": [ + "HP:0006677" + ], + "prolonged qrs complex on ekg": [ + "HP:0006677" + ], + "granulomatous coronary arteritis": [ + "HP:0006679" + ], + "absent atrioventricular node": [ + "HP:0006681" + ], + "premature ventricular contraction": [ + "HP:0006682" + ], + "extra heart beat": [ + "HP:0006682" + ], + "miss heartbeat": [ + "HP:0006682" + ], + "missed heartbeat": [ + "HP:0006682" + ], + "premature ventricular beat": [ + "HP:0006682" + ], + "premature ventricular contractions": [ + "HP:0006682" + ], + "skip heartbeat": [ + "HP:0006682" + ], + "skipped heartbeat": [ + "HP:0006682" + ], + "ventricular ectopics": [ + "HP:0006682" + ], + "ventricular extrasystole": [ + "HP:0006682" + ], + "ventricular extrasystoles": [ + "HP:0006682" + ], + "ventricular premature beat": [ + "HP:0006682" + ], + "abnormal ventricular filling": [ + "HP:0006683" + ], + "ventricular preexcitation with multiple accessory pathway": [ + "HP:0006684" + ], + "ventricular preexcitation with multiple accessory pathways": [ + "HP:0006684" + ], + "endocardial fibrosis": [ + "HP:0006685" + ], + "endomyocardial fibrosis": [ + "HP:0006685" + ], + "aortic tortuosity": [ + "HP:0006687" + ], + "paroxysmal tachycardia": [ + "HP:0006688" + ], + "bacterial endocarditis": [ + "HP:0006689" + ], + "infective endocarditis": [ + "HP:0006689" + ], + "myocardial calcification": [ + "HP:0006690" + ], + "calcified myocardium": [ + "HP:0006690" + ], + "pulmonic valve myxoma": [ + "HP:0006691" + ], + "short chordae tendineae of the tricuspid valve": [ + "HP:0006692" + ], + "myocardial steatosis": [ + "HP:0006693" + ], + "early progressive calcific cardiac valvular disease": [ + "HP:0006694" + ], + "atrioventricular canal defect": [ + "HP:0006695" + ], + "atrioventricular septal defect": [ + "HP:0006695" + ], + "endocardial cushion defect": [ + "HP:0006695" + ], + "hole in center of heart": [ + "HP:0006695" + ], + "hole in centre of heart": [ + "HP:0006695" + ], + "polymorphic and polytopic ventricular extrasystole": [ + "HP:0006696" + ], + "polymorphic and polytopic ventricular extrasystoles": [ + "HP:0006696" + ], + "dilatation of the ventricular cavity": [ + "HP:0006698" + ], + "ventricular aneurysm": [ + "HP:0006698" + ], + "premature atrial contraction": [ + "HP:0006699" + ], + "premature atrial contractions": [ + "HP:0006699" + ], + "atrial ectopic beat": [ + "HP:0006699" + ], + "atrial ectopic beats": [ + "HP:0006699" + ], + "atrial premature complex": [ + "HP:0006699" + ], + "ectopic supraventricular rhythm": [ + "HP:0006699" + ], + "ectopic supraventricular rhythms": [ + "HP:0006699" + ], + "pac": [ + "HP:0006699" + ], + "pacs": [ + "HP:0006699" + ], + "premature supraventricular beat": [ + "HP:0006699" + ], + "premature supraventricular beats": [ + "HP:0006699" + ], + "coronary artery dissection": [ + "HP:0006702" + ], + "aplasia / hypoplasia of the lung": [ + "HP:0006703" + ], + "aplasia / hypoplasia of the lungs": [ + "HP:0006703" + ], + "absent / small lung": [ + "HP:0006703" + ], + "absent / small lungs": [ + "HP:0006703" + ], + "absent / underdevelop lung": [ + "HP:0006703" + ], + "absent / underdeveloped lungs": [ + "HP:0006703" + ], + "abnormal coronary artery morphology": [ + "HP:0006704" + ], + "abnormal atrioventricular valve morphology": [ + "HP:0006705" + ], + "abnormality of the atrioventricular valve": [ + "HP:0006705" + ], + "abnormality of the atrioventricular valves": [ + "HP:0006705" + ], + "cystic liver disease": [ + "HP:0006706" + ], + "abnormality of the hepatic vasculature": [ + "HP:0006707" + ], + "abnormality of liver blood vessel": [ + "HP:0006707" + ], + "abnormality of liver blood vessels": [ + "HP:0006707" + ], + "abnormality of the liver vasculature": [ + "HP:0006707" + ], + "aplasia / hypoplasia of the nipple": [ + "HP:0006709" + ], + "aplasia / hypoplasia of the nipples": [ + "HP:0006709" + ], + "absent / rudimentary nipple": [ + "HP:0006709" + ], + "absent / rudimentary nipples": [ + "HP:0006709" + ], + "absent / small nipple": [ + "HP:0006709" + ], + "absent / small nipples": [ + "HP:0006709" + ], + "absent / underdevelop nipple": [ + "HP:0006709" + ], + "absent / underdeveloped nipples": [ + "HP:0006709" + ], + "nipple absent or rudimentary": [ + "HP:0006709" + ], + "nipples absent or rudimentary": [ + "HP:0006709" + ], + "aplasia / hypoplasia of the clavicle": [ + "HP:0006710" + ], + "aplasia / hypoplasia of the clavicles": [ + "HP:0006710" + ], + "absent / small collarbone": [ + "HP:0006710" + ], + "absent / underdevelop collarbone": [ + "HP:0006710" + ], + "absent / underdeveloped collarbone": [ + "HP:0006710" + ], + "aplasia / hypoplasia involve bone of the thorax": [ + "HP:0006711" + ], + "aplasia / hypoplasia involving bones of the thorax": [ + "HP:0006711" + ], + "absent / small outermost thorax bone": [ + "HP:0006711" + ], + "absent / underdevelop thorax bone": [ + "HP:0006711" + ], + "absent / underdeveloped thorax bone": [ + "HP:0006711" + ], + "aplasia / hypoplasia of the rib": [ + "HP:0006712" + ], + "aplasia / hypoplasia of the ribs": [ + "HP:0006712" + ], + "absent / small rib": [ + "HP:0006712" + ], + "absent / small ribs": [ + "HP:0006712" + ], + "absent / underdevelop rib": [ + "HP:0006712" + ], + "absent / underdeveloped ribs": [ + "HP:0006712" + ], + "hypoplastic or miss rib": [ + "HP:0006712" + ], + "hypoplastic or missing ribs": [ + "HP:0006712" + ], + "aplasia / hypoplasia of the scapula": [ + "HP:0006713" + ], + "aplasia / hypoplasia of the scapulae": [ + "HP:0006713" + ], + "absent / small shoulder blade": [ + "HP:0006713" + ], + "absent / underdevelop shoulder blade": [ + "HP:0006713" + ], + "absent / underdeveloped shoulder blade": [ + "HP:0006713" + ], + "aplasia / hypoplasia of the sternum": [ + "HP:0006714" + ], + "absent / small sternum": [ + "HP:0006714" + ], + "absent / underdevelop sternum": [ + "HP:0006714" + ], + "absent / underdeveloped sternum": [ + "HP:0006714" + ], + "glomus tympanicum paraganglioma": [ + "HP:0006715" + ], + "tympanic nerve tumor": [ + "HP:0006715" + ], + "tympanic nerve tumors": [ + "HP:0006715" + ], + "tympanic nerve tumour": [ + "HP:0006715" + ], + "tympanic nerve tumours": [ + "HP:0006715" + ], + "hereditary nonpolyposis colorectal carcinoma": [ + "HP:0006716" + ], + "peripheral neuroepithelioma": [ + "HP:0006717" + ], + "benign gastrointestinal tract tumor": [ + "HP:0006719" + ], + "benign gastrointestinal tract tumors": [ + "HP:0006719" + ], + "benign gastrointestinal tract tumour": [ + "HP:0006719" + ], + "benign gastrointestinal tract tumours": [ + "HP:0006719" + ], + "benign gi tract tumor": [ + "HP:0006719" + ], + "benign gi tract tumors": [ + "HP:0006719" + ], + "benign gi tract tumour": [ + "HP:0006719" + ], + "benign gi tract tumours": [ + "HP:0006719" + ], + "non - cancerous gi tumor": [ + "HP:0006719" + ], + "non - cancerous gi tumors": [ + "HP:0006719" + ], + "non - cancerous gi tumour": [ + "HP:0006719" + ], + "non - cancerous gi tumours": [ + "HP:0006719" + ], + "acute lymphoblastic leukemia": [ + "HP:0006721" + ], + "acute lymphatic leukaemia": [ + "HP:0006721" + ], + "acute lymphatic leukemia": [ + "HP:0006721" + ], + "acute lymphoblastic leukaemia": [ + "HP:0006721" + ], + "acute lymphocytic leukaemia": [ + "HP:0006721" + ], + "acute lymphocytic leukemia": [ + "HP:0006721" + ], + "acute lymphoid leukaemia": [ + "HP:0006721" + ], + "acute lymphoid leukemia": [ + "HP:0006721" + ], + "small intestine carcinoid": [ + "HP:0006722" + ], + "intestinal carcinoid": [ + "HP:0006723" + ], + "pancreatic adenocarcinoma": [ + "HP:0006725" + ], + "t - cell acute lymphoblastic leukemia": [ + "HP:0006727" + ], + "t - cell acute lymphoblastic leukemias": [ + "HP:0006727" + ], + "retroperitoneal chemodectomas": [ + "HP:0006729" + ], + "follicular thyroid carcinoma": [ + "HP:0006731" + ], + "papillary renal cell carcinoma type 2": [ + "HP:0006732" + ], + "acute megakaryocytic leukemia": [ + "HP:0006733" + ], + "acute megakaryocytic leukaemia": [ + "HP:0006733" + ], + "amegl": [ + "HP:0006733" + ], + "renal cortical adenoma": [ + "HP:0006735" + ], + "kidney cortical adenoma": [ + "HP:0006735" + ], + "extraadrenal pheochromocytoma": [ + "HP:0006737" + ], + "pheochromocytoma , extraadrenal": [ + "HP:0006737" + ], + "squamous cell carcinoma of the skin": [ + "HP:0006739" + ], + "squamous skin carcinoma": [ + "HP:0006739" + ], + "transitional cell carcinoma of the bladder": [ + "HP:0006740" + ], + "transitional cell bladder carcinoma": [ + "HP:0006740" + ], + "congenital neuroblastoma": [ + "HP:0006742" + ], + "embryonal rhabdomyosarcoma": [ + "HP:0006743" + ], + "adrenocortical carcinoma": [ + "HP:0006744" + ], + "adrenal carcinoma": [ + "HP:0006744" + ], + "adrenal gland carinoma": [ + "HP:0006744" + ], + "ganglioneuroblastoma": [ + "HP:0006747" + ], + "adrenal pheochromocytoma": [ + "HP:0006748" + ], + "pheochromocytoma , adrenal": [ + "HP:0006748" + ], + "pheochromocytomas , adrenal": [ + "HP:0006748" + ], + "malignant gastrointestinal tract tumor": [ + "HP:0006749" + ], + "malignant gastrointestinal tract tumors": [ + "HP:0006749" + ], + "malignant gastrointestinal tract tumour": [ + "HP:0006749" + ], + "malignant gastrointestinal tract tumours": [ + "HP:0006749" + ], + "malignant gi tract tumor": [ + "HP:0006749" + ], + "malignant gi tract tumors": [ + "HP:0006749" + ], + "malignant gi tract tumour": [ + "HP:0006749" + ], + "malignant gi tract tumours": [ + "HP:0006749" + ], + "paraspinal neurofibroma": [ + "HP:0006751" + ], + "paraspinal neurofibromas": [ + "HP:0006751" + ], + "neoplasm of the stomach": [ + "HP:0006753" + ], + "neoplasia of the stomach": [ + "HP:0006753" + ], + "stomach tumor": [ + "HP:0006753" + ], + "stomach tumour": [ + "HP:0006753" + ], + "cutaneous leiomyosarcoma": [ + "HP:0006755" + ], + "diffuse leiomyomatosis": [ + "HP:0006756" + ], + "malignant genitourinary tract tumor": [ + "HP:0006758" + ], + "malignant genitourinary tract tumour": [ + "HP:0006758" + ], + "malignant gu tract tumor": [ + "HP:0006758" + ], + "malignant gu tract tumour": [ + "HP:0006758" + ], + "renal pelvic carcinoma": [ + "HP:0006762" + ], + "anal canal squamous carcinoma": [ + "HP:0006763" + ], + "chondrosarcoma": [ + "HP:0006765" + ], + "papillary renal cell carcinoma": [ + "HP:0006766" + ], + "pituitary prolactin cell adenoma": [ + "HP:0006767" + ], + "pituitary prolactinoma": [ + "HP:0006767" + ], + "prolactin - secrete pituitary adenoma": [ + "HP:0006767" + ], + "prolactin - secreting pituitary adenoma": [ + "HP:0006767" + ], + "localize neuroblastoma": [ + "HP:0006768" + ], + "localized neuroblastoma": [ + "HP:0006768" + ], + "localise neuroblastoma": [ + "HP:0006768" + ], + "localised neuroblastoma": [ + "HP:0006768" + ], + "myxoid subcutaneous tumor": [ + "HP:0006769" + ], + "myxoid subcutaneous tumors": [ + "HP:0006769" + ], + "myxoid subcutaneous tumour": [ + "HP:0006769" + ], + "myxoid subcutaneous tumours": [ + "HP:0006769" + ], + "clear cell renal cell carcinoma": [ + "HP:0006770" + ], + "nonpapillary renal cell carcinoma": [ + "HP:0006770" + ], + "duodenal adenocarcinoma": [ + "HP:0006771" + ], + "duodenal cancer": [ + "HP:0006771" + ], + "renal angiomyolipoma": [ + "HP:0006772" + ], + "angiomyolipoma": [ + "HP:0006772" + ], + "kidney angiomyolipoma": [ + "HP:0006772" + ], + "cutaneous angiolipomas": [ + "HP:0006773" + ], + "ovarian papillary adenocarcinoma": [ + "HP:0006774" + ], + "multiple myeloma": [ + "HP:0006775" + ], + "kahler 's disease": [ + "HP:0006775" + ], + "plasmocytoma": [ + "HP:0006775" + ], + "benign genitourinary tract neoplasm": [ + "HP:0006778" + ], + "benign genitourinary tract tumor": [ + "HP:0006778" + ], + "benign genitourinary tract tumour": [ + "HP:0006778" + ], + "benign gu tract neoplasm": [ + "HP:0006778" + ], + "alveolar rhabdomyosarcoma": [ + "HP:0006779" + ], + "parathyroid carcinoma": [ + "HP:0006780" + ], + "parathyroid cancer": [ + "HP:0006780" + ], + "hurthle cell thyroid adenoma": [ + "HP:0006781" + ], + "malignant eosinophil proliferation": [ + "HP:0006782" + ], + "posterior pharyngeal cleft": [ + "HP:0006783" + ], + "paranasal sinus hypoplasia": [ + "HP:0006784" + ], + "atelectasis of paranasal sinus": [ + "HP:0006784" + ], + "decreased growth of paranasal sinus": [ + "HP:0006784" + ], + "decreased pneumatization of paranasal sinus": [ + "HP:0006784" + ], + "decreased size of paranasal sinus": [ + "HP:0006784" + ], + "decreased volume of paranasal sinus": [ + "HP:0006784" + ], + "hypotrophic paranasal sinus": [ + "HP:0006784" + ], + "small paranasal sinus": [ + "HP:0006784" + ], + "underdevelopment of paranasal sinus": [ + "HP:0006784" + ], + "limb - girdle muscular dystrophy": [ + "HP:0006785" + ], + "limb girdle muscular dystrophy": [ + "HP:0006785" + ], + "mitochondrial encephalopathy": [ + "HP:0006789" + ], + "cerebral cortex with spongiform change": [ + "HP:0006790" + ], + "cerebral cortex with spongiform changes": [ + "HP:0006790" + ], + "loss of ability to walk in first decade": [ + "HP:0006794" + ], + "basal ganglion cyst": [ + "HP:0006799" + ], + "basal ganglia cysts": [ + "HP:0006799" + ], + "cystic lesion in the basal ganglion": [ + "HP:0006799" + ], + "cystic lesions in the basal ganglia": [ + "HP:0006799" + ], + "hyperactive deep tendon reflex": [ + "HP:0006801" + ], + "hyperactive deep tendon reflexes": [ + "HP:0006801" + ], + "abnormal anterior horn cell morphology": [ + "HP:0006802" + ], + "abnormality of the anterior horn cell": [ + "HP:0006802" + ], + "abnormality of the anterior horn cells": [ + "HP:0006802" + ], + "anomaly of the anterior horn cell": [ + "HP:0006802" + ], + "anomaly of the anterior horn cells": [ + "HP:0006802" + ], + "anterior horn cell disease": [ + "HP:0006802" + ], + "vivid hallucination": [ + "HP:0006803" + ], + "vivid hallucinations": [ + "HP:0006803" + ], + "cerebral hypomyelination": [ + "HP:0006808" + ], + "hypomyelination of the brain": [ + "HP:0006808" + ], + "white mater abnormality in the posterior periventricular region": [ + "HP:0006812" + ], + "white mater abnormalities in the posterior periventricular region": [ + "HP:0006812" + ], + "focal hemiclonic seizure": [ + "HP:0006813" + ], + "hemiclonic seizure": [ + "HP:0006813" + ], + "hemiclonic seizures": [ + "HP:0006813" + ], + "unilateral clonic seizure": [ + "HP:0006813" + ], + "unilateral clonic seizures": [ + "HP:0006813" + ], + "aplasia / hypoplasia of the cerebellar vermis": [ + "HP:0006817" + ], + "cerebellar vermis aplasia or hypoplasia": [ + "HP:0006817" + ], + "cerebellar vermis aplasia / hypoplasia": [ + "HP:0006817" + ], + "hypo / aplastic vermis": [ + "HP:0006817" + ], + "4 - layer lissencephaly": [ + "HP:0006818" + ], + "4 - layered lissencephaly": [ + "HP:0006818" + ], + "classic lissencephaly": [ + "HP:0006818" + ], + "four - layer lissencephaly": [ + "HP:0006818" + ], + "four - layered lissencephaly": [ + "HP:0006818" + ], + "lissencephaly , type i": [ + "HP:0006818" + ], + "type 1 lissencephaly": [ + "HP:0006818" + ], + "type i lissencephaly": [ + "HP:0006818" + ], + "frontal polymicrogyria": [ + "HP:0006821" + ], + "polymicrogyria , anterior to posterior gradient": [ + "HP:0006821" + ], + "cranial nerve paralysis": [ + "HP:0006824" + ], + "cranial nerve palsy": [ + "HP:0006824" + ], + "cranial nerve palsies": [ + "HP:0006824" + ], + "cranial nerve paresis": [ + "HP:0006824" + ], + "pallor of dorsal column of the spinal cord": [ + "HP:0006825" + ], + "pallor of dorsal columns of the spinal cord": [ + "HP:0006825" + ], + "atrophy of the spinal cord": [ + "HP:0006827" + ], + "degeneration of the spinal cord": [ + "HP:0006827" + ], + "severe muscular hypotonia": [ + "HP:0006829" + ], + "hypotonia , severe": [ + "HP:0006829" + ], + "severely decreased muscle tone": [ + "HP:0006829" + ], + "obsolete severe neonatal hypotonia in male": [ + "HP:0006830" + ], + "obsolete severe neonatal hypotonia in males": [ + "HP:0006830" + ], + "developmental stagnation at onset of seizure": [ + "HP:0006834" + ], + "developmental 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lissencephaly": [ + "HP:0007260" + ], + "cobblestone lissencephaly": [ + "HP:0007260" + ], + "lissencephaly type ii": [ + "HP:0007260" + ], + "type 2 lissencephaly": [ + "HP:0007260" + ], + "symmetric peripheral demyelination": [ + "HP:0007262" + ], + "spinocerebellar atrophy": [ + "HP:0007263" + ], + "absent mesencephalon": [ + "HP:0007265" + ], + "cerebral dysmyelination": [ + "HP:0007266" + ], + "area of dysmyelination on mri": [ + "HP:0007266" + ], + "areas of dysmyelination on mri": [ + "HP:0007266" + ], + "dysmyelination of the brain": [ + "HP:0007266" + ], + "white matter dysmyelination / demyelination": [ + "HP:0007266" + ], + "chronic axonal neuropathy": [ + "HP:0007267" + ], + "chronic sural axonal neuropathy": [ + "HP:0007267" + ], + "aprosencephaly": [ + "HP:0007268" + ], + "spinal muscular atrophy": [ + "HP:0007269" + ], + "spinal muscle degeneration": [ + "HP:0007269" + ], + "spinal muscle waste": [ + "HP:0007269" + ], + "spinal muscle wasting": [ + "HP:0007269" + ], + 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bones": [ + "HP:0007285" + ], + "facial palsy cause by excessive growth of facial bone": [ + "HP:0007285" + ], + "facial palsy caused by excessive growth of facial bones": [ + "HP:0007285" + ], + "facial palsy cause by overgrowth of cranial bone": [ + "HP:0007285" + ], + "facial palsy caused by overgrowth of cranial bones": [ + "HP:0007285" + ], + "facial palsy secondary to hypertrophy of cranial bone": [ + "HP:0007285" + ], + "facial palsy secondary to hypertrophy of cranial bones": [ + "HP:0007285" + ], + "horizontal jerk nystagmus": [ + "HP:0007286" + ], + "limb fasciculation": [ + "HP:0007289" + ], + "limb fasciculations": [ + "HP:0007289" + ], + "posterior fossa cyst": [ + "HP:0007291" + ], + "anterior sacral meningocele": [ + "HP:0007293" + ], + "chaotic rapid conjugate ocular movement": [ + "HP:0007295" + ], + "chaotic rapid conjugate ocular movements": [ + "HP:0007295" + ], + "dysfunction of lateral corticospinal tract": [ + "HP:0007299" + ], + "dysfunction of lateral corticospinal tracts": [ + "HP:0007299" + ], + "oromotor apraxia": [ + "HP:0007301" + ], + "bipolar affective disorder": [ + "HP:0007302" + ], + "bipolar disorder": [ + "HP:0007302" + ], + "cns demyelination": [ + "HP:0007305" + ], + "demyelination in central white matter": [ + "HP:0007305" + ], + "rapid neurologic deterioration": [ + "HP:0007307" + ], + "extrapyramidal dyskinesia": [ + "HP:0007308" + ], + "short step shuffle gait": [ + "HP:0007311" + ], + "short stepped shuffling gait": [ + "HP:0007311" + ], + "short step shuffle walk": [ + "HP:0007311" + ], + "short stepped shuffling walk": [ + "HP:0007311" + ], + "cerebral degeneration": [ + "HP:0007313" + ], + "neuroaxonal degeneration in the brain": [ + "HP:0007313" + ], + "obsolete white matter neuronal heterotopia": [ + "HP:0007314" + ], + "obsolete involuntary writhing movement": [ + "HP:0007316" + ], + "obsolete involuntary writhing movements": [ + "HP:0007316" + ], + "deep white matter hypodensities": [ + "HP:0007321" + ], + "deep cerebral white matter hypodensities": [ + "HP:0007321" + ], + "generalize dystonia": [ + "HP:0007325" + ], + "generalized dystonia": [ + "HP:0007325" + ], + "generalise dystonia": [ + "HP:0007325" + ], + "generalised dystonia": [ + "HP:0007325" + ], + "progressive choreoathetosis": [ + "HP:0007326" + ], + "mixed demyelinating and axonal polyneuropathy": [ + "HP:0007327" + ], + "impaired pain sensation": [ + "HP:0007328" + ], + "decrease pain sensation": [ + "HP:0007328" + ], + "decreased pain sensation": [ + "HP:0007328" + ], + "decrease pinprick sensation": [ + "HP:0007328" + ], + "decreased pinprick sensation": [ + "HP:0007328" + ], + "frontal encephalocele": [ + "HP:0007330" + ], + "focal hemifacial clonic seizure": [ + "HP:0007332" + ], + "hemifacial seizure": [ + "HP:0007332" + ], + "hemifacial seizures": [ + "HP:0007332" + ], + "hypoplasia of the frontal lobe": [ + "HP:0007333" + ], + "hypoplasia of the frontal lobes": [ + "HP:0007333" + ], + "frontal lobe hypoplasia": [ + 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focal onset": [ + "HP:0007334" + ], + "generalized tonic - clonic seizures with focal onset": [ + "HP:0007334" + ], + "partial seizure with secondary generalisation": [ + "HP:0007334" + ], + "partial seizure with secondary generalization": [ + "HP:0007334" + ], + "partial seizures with secondary generalisation": [ + "HP:0007334" + ], + "partial seizures with secondary generalization": [ + "HP:0007334" + ], + "secondarily generalise tonic - clonic seizure": [ + "HP:0007334" + ], + "secondarily generalised tonic - clonic seizure": [ + "HP:0007334" + ], + "secondarily generalised tonic - clonic seizures": [ + "HP:0007334" + ], + "secondarily generalize tonic - clonic seizure": [ + "HP:0007334" + ], + "secondarily generalized tonic - clonic seizure": [ + "HP:0007334" + ], + "secondary generalise tonic clonic seizure": [ + "HP:0007334" + ], + "secondary generalised tonic clonic seizures": [ + "HP:0007334" + ], + "secondary generalise tonic - clonic seizure": [ + "HP:0007334" + ], + "secondary generalised tonic - clonic seizures": [ + "HP:0007334" + ], + "secondary generalize tonic clonic seizure": [ + "HP:0007334" + ], + "secondary generalized tonic clonic seizures": [ + "HP:0007334" + ], + "secondary generalize tonic - clonic seizure": [ + "HP:0007334" + ], + "secondary generalized tonic - clonic seizures": [ + "HP:0007334" + ], + "recurrent encephalopathy": [ + "HP:0007335" + ], + "recurrent cerebellar and extrapyramidal encephalopathy": [ + "HP:0007335" + ], + "hypermetric saccade": [ + "HP:0007338" + ], + "hypermetric saccades": [ + "HP:0007338" + ], + "low limb muscle weakness": [ + "HP:0007340" + ], + "lower limb muscle weakness": [ + "HP:0007340" + ], + "leg weakness": [ + "HP:0007340" + ], + "low extremity weakness": [ + "HP:0007340" + ], + "lower extremity weakness": [ + "HP:0007340" + ], + "low limb weakness": [ + "HP:0007340" + ], + "lower limb weakness": [ + "HP:0007340" + ], + "muscle weakness in low limb": [ + "HP:0007340" + ], + "muscle weakness in lower limbs": [ + "HP:0007340" + ], + "diffuse swelling of cerebral white matter": [ + "HP:0007341" + ], + "abnormal morphology of the limbic system": [ + "HP:0007343" + ], + "limbic malformation": [ + "HP:0007343" + ], + "atrophy / degeneration involve the spinal cord": [ + "HP:0007344" + ], + "atrophy / degeneration involving the spinal cord": [ + "HP:0007344" + ], + "atrophic and degenerative change in the spinal cord": [ + "HP:0007344" + ], + "atrophic and degenerative changes in the spinal cord": [ + "HP:0007344" + ], + "subcortical white matter calcification": [ + "HP:0007346" + ], + "subcortical white matter calcifications": [ + "HP:0007346" + ], + "hypoplasia of the pyramidal tract": [ + "HP:0007348" + ], + "hyperreflexia in upper limb": [ + "HP:0007350" + ], + "hyperreflexia in upper limbs": [ + "HP:0007350" + ], + "upper limb postural tremor": [ + "HP:0007351" + ], + "postural tremor of arm": [ + "HP:0007351" + ], + "postural tremor of arms": [ + "HP:0007351" + ], + "cerebellar calcification": [ + "HP:0007352" + ], + "cerebellar calcifications": [ + "HP:0007352" + ], + "amyotrophic lateral sclerosis": [ + "HP:0007354" + ], + "lou gehrig 's disease": [ + "HP:0007354" + ], + "focal - onset seizure": [ + "HP:0007359" + ], + "focal onset seizure": [ + "HP:0007359" + ], + "focal seizure": [ + "HP:0007359" + ], + "focal seizures": [ + "HP:0007359" + ], + "focal - onset seizures": [ + "HP:0007359" + ], + "partial seizure": [ + "HP:0007359" + ], + "partial seizures": [ + "HP:0007359" + ], + "seizure affect one half of brain": [ + "HP:0007359" + ], + "seizure affecting one half of brain": [ + "HP:0007359" + ], + "aplasia / hypoplasia of the cerebellum": [ + "HP:0007360" + ], + "absent / small cerebellum": [ + "HP:0007360" + ], + "absent / underdevelop cerebellum": [ + "HP:0007360" + ], + "absent / underdeveloped cerebellum": [ + "HP:0007360" + ], + "atrophy / degeneration affect the cerebellum": [ + "HP:0007360" + ], + "atrophy / degeneration affecting the cerebellum": [ + "HP:0007360" + ], + "atrophy / hypoplasia of the cerebellum": [ + "HP:0007360" + ], + "cerebellar hypoplasia / atrophy": [ + "HP:0007360" + ], + "abnormal pons morphology": [ + "HP:0007361" + ], + "abnormality of the pons": [ + "HP:0007361" + ], + "aplasia / hypoplasia of the brainstem": [ + "HP:0007362" + ], + "absent / small brainstem": [ + "HP:0007362" + ], + "absent / underdevelop brainstem": [ + "HP:0007362" + ], + "absent / underdeveloped brainstem": [ + "HP:0007362" + ], + "aplasia / hypoplasia of the pyramidal tract": [ + "HP:0007363" + ], + "aplasia / hypoplasia of the cerebrum": [ + "HP:0007364" + ], + "absent / small cerebrum": [ + "HP:0007364" + ], + "absent / underdevelop cerebrum": [ + "HP:0007364" + ], + "absent / underdeveloped cerebrum": [ + "HP:0007364" + ], + "aplasia / hypoplasia involve the corticospinal tract": [ + "HP:0007365" + ], + "aplasia / hypoplasia involving the corticospinal tracts": [ + "HP:0007365" + ], + "atrophy / degeneration affect the brainstem": [ + "HP:0007366" + ], + "atrophy / degeneration affecting the brainstem": [ + "HP:0007366" + ], + "brainstem atrophy": [ + "HP:0007366" + ], + "atrophy / degeneration affect the central nervous system": [ + "HP:0007367" + ], + "atrophy / degeneration affecting the central nervous system": [ + "HP:0007367" + ], + "atrophy / degeneration affect the cns": [ + "HP:0007367" + ], + "atrophy / degeneration affecting the cns": [ + "HP:0007367" + ], + "atrophy / degeneration affect the cerebrum": [ + "HP:0007369" + ], + "atrophy / degeneration affecting the cerebrum": [ + "HP:0007369" + ], + "aplasia / hypoplasia of the corpus callosum": [ + "HP:0007370" + ], + "absent / hypoplastic corpus callosum": [ + "HP:0007370" + ], + "agenesis / hypoplastic corpus callosum": [ + "HP:0007370" + ], + "complete or partial absence of the corpus callosum": [ + "HP:0007370" + ], + "hypoplasia or absence of the corpus callosum": [ + "HP:0007370" + ], + "hypoplastic or absent corpus callosum": [ 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+ "neoplasm of the gastrointestinal tract": [ + "HP:0007378" + ], + "gastrointestinal tract neoplasia": [ + "HP:0007378" + ], + "gastrointestinal tract neoplasm": [ + "HP:0007378" + ], + "gastrointestinal tract tumor": [ + "HP:0007378" + ], + "gastrointestinal tract tumour": [ + "HP:0007378" + ], + "gi tract tumor": [ + "HP:0007378" + ], + "gi tract tumour": [ + "HP:0007378" + ], + "neoplasm of the gi tract": [ + "HP:0007378" + ], + "neoplasm of the genitourinary tract": [ + "HP:0007379" + ], + "genitourinary tract neoplasia": [ + "HP:0007379" + ], + "genitourinary tract neoplasm": [ + "HP:0007379" + ], + "genitourinary tract tumor": [ + "HP:0007379" + ], + "genitourinary tract tumors": [ + "HP:0007379" + ], + "genitourinary tract tumour": [ + "HP:0007379" + ], + "genitourinary tract tumours": [ + "HP:0007379" + ], + "neoplasm of the gu tract": [ + "HP:0007379" + ], + "facial telangiectasia": [ + "HP:0007380" + ], + "facial telangiectatic vessel": [ + "HP:0007380" + ], + "facial telangiectatic vessels": [ + "HP:0007380" + ], + "telangiectasia , facial": [ + "HP:0007380" + ], + "congenital exfoliative erythroderma": [ + "HP:0007381" + ], + "congenital localize absence of skin": [ + "HP:0007383" + ], + "congenital localized absence of skin": [ + "HP:0007383" + ], + "congenital localise absence of skin": [ + "HP:0007383" + ], + "congenital localised absence of skin": [ + "HP:0007383" + ], + "congenital localise skin absence": [ + "HP:0007383" + ], + "congenital localised skin absence": [ + "HP:0007383" + ], + "congenital localize skin absence": [ + "HP:0007383" + ], + "congenital localized skin absence": [ + "HP:0007383" + ], + "aberrant melanosome maturation": [ + "HP:0007384" + ], + "aplasia cutis congenita of scalp": [ + "HP:0007385" + ], + "defect of scalp": [ + "HP:0007385" + ], + "focal absence of scalp tissue": [ + "HP:0007385" + ], + "scalp aplasia cutis congenita": [ + "HP:0007385" + ], + "scalp defect": [ + "HP:0007385" + ], + "solitary scalp defect": [ 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"HP:0007398" + ], + "asymmetric , linear skin defects": [ + "HP:0007398" + ], + "irregular hyperpigmentation": [ + "HP:0007400" + ], + "macular atrophy": [ + "HP:0007401" + ], + "area of hypopigmentation and hyperpigmentation that do not follow blaschko line": [ + "HP:0007402" + ], + "areas of hypopigmentation and hyperpigmentation that do not follow blaschko lines": [ + "HP:0007402" + ], + "hypertrophy of skin of sol": [ + "HP:0007403" + ], + "hypertrophy of skin of soles": [ + "HP:0007403" + ], + "thick skin of sol": [ + "HP:0007403" + ], + "thick skin of soles": [ + "HP:0007403" + ], + "nonepidermolytic palmoplantar hyperkeratosis": [ + "HP:0007404" + ], + "nonepidermolytic palmoplantar keratoderma": [ + "HP:0007404" + ], + "hyperpigmentation of eyelid": [ + "HP:0007406" + ], + "hyperpigmentation of eyelids": [ + "HP:0007406" + ], + "brown eyelid": [ + "HP:0007406" + ], + "brown eyelids": [ + "HP:0007406" + ], + "dark eyelid": [ + "HP:0007406" + ], + "dark eyelids": [ + "HP:0007406" + ], + "pigmentation of eyelid": [ + "HP:0007406" + ], + "pigmentation of eyelids": [ + "HP:0007406" + ], + "excessive skin wrinkle on dorsum of hand and finger": [ + "HP:0007407" + ], + "excessive skin wrinkling on dorsum of hands and fingers": [ + "HP:0007407" + ], + "excessive skin wrinkle on back of hand and finger": [ + "HP:0007407" + ], + "excessive skin wrinkling on back of hands and fingers": [ + "HP:0007407" + ], + "tegumentary leishmaniasis susceptibility": [ + "HP:0007408" + ], + "obsolete absence of subcutaneous fat over entire body except buttock , hip , and thigh": [ + "HP:0007409" + ], + "obsolete absence of subcutaneous fat over entire body except buttocks , hips , and thighs": [ + "HP:0007409" + ], + "palmoplantar hyperhidrosis": [ + "HP:0007410" + ], + "excessive sweating of palm and sol": [ + "HP:0007410" + ], + "excessive sweating of palms and soles": [ + "HP:0007410" + ], + "hyperhidrosis of palm and sol": [ + "HP:0007410" + ], + "hyperhidrosis of palms and soles": [ + "HP:0007410" + ], + "hypoplastic - absent sebaceous gland": [ + "HP:0007411" + ], + "hypoplastic - absent sebaceous glands": [ + "HP:0007411" + ], + "macular hyperpigmented dermopathy": [ + "HP:0007412" + ], + "nevus flammeus of the forehead": [ + "HP:0007413" + ], + "port - wine stain on forehead": [ + "HP:0007413" + ], + "neonatal wrinkle skin of hand and foot": [ + "HP:0007414" + ], + "neonatal wrinkled skin of hands and feet": [ + "HP:0007414" + ], + "wrinkled skin of hand and foot in newborn": [ + "HP:0007414" + ], + "wrinkled skin of hands and feet in newborn": [ + "HP:0007414" + ], + "discoid lupus rash": [ + "HP:0007417" + ], + "discoid lupus erythematosus": [ + "HP:0007417" + ], + "alopecia totalis": [ + "HP:0007418" + ], + "total alopecia": [ + "HP:0007418" + ], + "spontaneous hematoma": [ + "HP:0007420" + ], + "spontaneous hematomas": [ + "HP:0007420" + ], + "telangiectases of the cheek": [ + "HP:0007421" + ], + "telangiectases of the cheeks": [ + "HP:0007421" + ], + "telangiectasia on the cheek": [ + "HP:0007421" + ], + "telangiectasia on the cheeks": [ + "HP:0007421" + ], + "hyperextensible skin of face": [ + "HP:0007425" + ], + "hyperelastic face skin": [ + "HP:0007425" + ], + "stretchable face skin": [ + "HP:0007425" + ], + "reticulate skin pigmentation": [ + "HP:0007427" + ], + "reticulated skin pigmentation": [ + "HP:0007427" + ], + "reticular pigmentation pattern": [ + "HP:0007427" + ], + "telangiectasia of the oral mucosa": [ + "HP:0007428" + ], + "angioectasia of the oral mucosa": [ + "HP:0007428" + ], + "angioectasia of the oral mucous membrane": [ + "HP:0007428" + ], + "spider vein of the oral mucosa": [ + "HP:0007428" + ], + "spider veins of the oral mucosa": [ + "HP:0007428" + ], + "telangiectasia of the oral mucous membrane": [ + "HP:0007428" + ], + "few cafe - au - lait spot": [ + "HP:0007429" + ], + "few cafe - au - lait spots": [ + "HP:0007429" + ], + "generalize edema": [ + "HP:0007430" + ], + "generalized edema": [ + "HP:0007430" + ], + "generalise oedema": [ + "HP:0007430" + ], + "generalised oedema": [ + "HP:0007430" + ], + "generalise tissue oedema": [ + "HP:0007430" + ], + "generalised tissue oedema": [ + "HP:0007430" + ], + "generalize tissue edema": [ + "HP:0007430" + ], + "generalized tissue edema": [ + "HP:0007430" + ], + "congenital ichthyosiform erythroderma": [ + "HP:0007431" + ], + "congenital ichthyosis": [ + "HP:0007431" + ], + "ichthyosis , congenital": [ + "HP:0007431" + ], + "intermittent generalize erythematous papular rash": [ + "HP:0007432" + ], + "intermittent generalized erythematous papular rash": [ + "HP:0007432" + ], + "intermittent generalise erythematous papular rash": [ + "HP:0007432" + ], + "intermittent generalised erythematous papular rash": [ + "HP:0007432" + ], + "plaque - like facial hemangioma": [ + "HP:0007434" + ], + "hemangioma , facial , plaque - like": [ + "HP:0007434" + ], + "obsolete diffuse palmoplantar keratoderma": [ + "HP:0007435" + ], + "hair - nail ectodermal dysplasia": [ + "HP:0007436" + ], + "multiple cutaneous leiomyoma": [ + "HP:0007437" + ], + "multiple cutaneous leiomyomas": [ + "HP:0007437" + ], + "mottle pigmentation of the trunk and proximal extremity": [ + "HP:0007438" + ], + "mottled pigmentation of the trunk and proximal extremities": [ + "HP:0007438" + ], + "generalize keratosis follicularis": [ + "HP:0007439" + ], + "generalized keratosis follicularis": [ + "HP:0007439" + ], + "generalise keratosis follicularis": [ + "HP:0007439" + ], + "generalised keratosis follicularis": [ + "HP:0007439" + ], + "generalize hyperpigmentation": [ + "HP:0007440" + ], + "generalized hyperpigmentation": [ + "HP:0007440" + ], + "generalise hyperpigmentation": [ + "HP:0007440" + ], + "generalised hyperpigmentation": [ + "HP:0007440" + ], + "hyperpigmented / hypopigmented macule": [ + "HP:0007441" + ], + "hyperpigmented / hypopigmented macules": [ + "HP:0007441" + ], + "partial albinism": [ + "HP:0007443" + ], + "congenital partial albinism on face , trunk , or limb": [ + "HP:0007443" + ], + "congenital partial albinism on face , trunk , or limbs": [ + "HP:0007443" + ], + "congenital partial leucoderma": [ + "HP:0007443" + ], + "partial absent skin pigmentation": [ + "HP:0007443" + ], + "palmoplantar blistering": [ + "HP:0007446" + ], + "diffuse palmoplantar hyperkeratosis": [ + "HP:0007447" + ], + "diffuse palmoplantar keratoderma": [ + "HP:0007447" + ], + "hyperkeratosis , diffuse palmoplantar": [ + "HP:0007447" + ], + "hyperkeratosis over edematous area": [ + "HP:0007448" + ], + "hyperkeratosis over edematous areas": [ + "HP:0007448" + ], + "confetti - like hypopigmented macule": [ + "HP:0007449" + ], + "confetti - like hypopigmented macules": [ + "HP:0007449" + ], + "increase groin pigmentation with raindrop depigmentation": [ + "HP:0007450" + ], + "increased groin pigmentation with raindrop depigmentation": [ + "HP:0007450" + ], + "ipsilateral lack of facial sweating": [ + "HP:0007451" + ], + "midface capillary hemangioma": [ + "HP:0007452" + ], + "midfacial capillary hemangioma": [ + "HP:0007452" + ], + "flexural lichenification": [ + "HP:0007453" + ], + "adermatoglyphia": [ + "HP:0007455" + ], + "progressive reticulate hyperpigmentation": [ + "HP:0007456" + ], + "prominent vein on trunk": [ + "HP:0007457" + ], + "prominent veins on trunk": [ + "HP:0007457" + ], + "focal hyperextensible skin": [ + "HP:0007458" + ], + "generalize anhidrosis": [ + "HP:0007459" + ], + "generalized anhidrosis": [ + "HP:0007459" + ], + "generalise anhidrosis": [ + "HP:0007459" + ], + "generalised anhidrosis": [ + "HP:0007459" + ], + "generalise anhydrosis": [ + "HP:0007459" + ], + "generalised anhydrosis": [ + "HP:0007459" + ], + "generalise inability to sweat": [ + "HP:0007459" + ], + "generalised inability to sweat": [ + "HP:0007459" + ], + "generalize anhydrosis": [ + "HP:0007459" + ], + "generalized anhydrosis": [ + "HP:0007459" + ], + "generalize inability to sweat": [ + "HP:0007459" + ], + "generalized inability to sweat": [ + "HP:0007459" + ], + "autoamputation of digit": [ + "HP:0007460" + ], + "autoamputation of digits": [ + "HP:0007460" + ], + "hemangiomatosis": [ + "HP:0007461" + ], + "bitot spot of the conjunctiva": [ + "HP:0007462" + ], + "bitot spots of the conjunctiva": [ + "HP:0007462" + ], + "bitot 's spot": [ + "HP:0007462" + ], + "bitot 's spots": [ + "HP:0007462" + ], + "sparse facial hair": [ + "HP:0007464" + ], + "honeycomb palmoplantar hyperkeratosis": [ + "HP:0007465" + ], + "midfrontal capillary hemangioma": [ + "HP:0007466" + ], + "perifollicular hyperkeratosis": [ + "HP:0007468" + ], + "palmoplantar cutis gyrata": [ + "HP:0007469" + ], + "cutis gyrata of palm and sol": [ + "HP:0007469" + ], + "cutis gyrata of palms and soles": [ + "HP:0007469" + ], + "periarticular subcutaneous nodule": [ + "HP:0007470" + ], + "periarticular subcutaneous nodules": [ + "HP:0007470" + ], + "axillary and groin hyperpigmentation and hypopigmentation": [ + "HP:0007471" + ], + "crust erythematous dermatitis": [ + "HP:0007473" + ], + "crusting erythematous dermatitis": [ + "HP:0007473" + ], + "congenital bullous ichthyosiform erythroderma": [ + "HP:0007475" + ], + "bullous congenital ichthyosiform erythroderma": [ + "HP:0007475" + ], + "epidermolytic hyperkeratosis": [ + "HP:0007475" + ], + "anhidrotic ectodermal dysplasia": [ + "HP:0007476" + ], + "abnormal dermatoglyphic": [ + "HP:0007477" + ], + "abnormal dermatoglyphics": [ + "HP:0007477" + ], + "abnormal fingerprint": [ + "HP:0007477" + ], + "abnormal fingerprints": [ + "HP:0007477" + ], + "dermatoglyphic abnormality": [ + "HP:0007477" + ], + "dermatoglyphic abnormalities": [ + "HP:0007477" + ], + "congenital nonbullous ichthyosiform erythroderma": [ + "HP:0007479" + ], + "collodion baby": [ + "HP:0007479" + ], + "congenital lamellar ichthyosis": [ + "HP:0007479" + ], + "congenital non - bullous ichthyosis": [ + "HP:0007479" + ], + "ichthyosis lammellaris": [ + "HP:0007479" + ], + "ichthyosis , congenital , nonblistering": [ + "HP:0007479" + ], + "nonbullous congenital ichthyosiform erythroderma": [ + "HP:0007479" + ], + "nonbullous congenital ichthyosis": [ + "HP:0007479" + ], + "decrease sweat due to autonomic dysfunction": [ + "HP:0007480" + ], + "decreased sweating due to autonomic dysfunction": [ + "HP:0007480" + ], + "hyperpigmented nevus": [ + "HP:0007481" + ], + "hyperpigmented nevi": [ + "HP:0007481" + ], + "generalize papillary lesion": [ + "HP:0007482" + ], + "generalized papillary lesions": [ + "HP:0007482" + ], + "generalise papillary lesion": [ + "HP:0007482" + ], + "generalised papillary lesions": [ + "HP:0007482" + ], + "depigmentation / hyperpigmentation of skin": [ + "HP:0007483" + ], + "absence of subcutaneous fat": [ + "HP:0007485" + ], + "absent fat below the skin": [ + "HP:0007485" + ], + "general absence of subcutaneous fat": [ + "HP:0007485" + ], + "lack of fatty tissue below the skin": [ + "HP:0007485" + ], + "cavernous hemangioma of the face": [ + "HP:0007486" + ], + "diffuse skin atrophy": [ + "HP:0007488" + ], + "diffuse telangiectasia": [ + "HP:0007489" + ], + "diffuse telangiectases": [ + "HP:0007489" + ], + "telangiectases , random body distribution": [ + "HP:0007489" + ], + "linear array of macular hyperkeratoses in flexural area": [ + "HP:0007490" + ], + "linear arrays of macular hyperkeratoses in flexural areas": [ + "HP:0007490" + ], + "discrete 2 to 5 - mm hyper - and hypopigmented macule": [ + "HP:0007494" + ], + "discrete 2 to 5 - mm hyper - and hypopigmented macules": [ + "HP:0007494" + ], + "prematurely age appearance": [ + "HP:0007495" + ], + "prematurely aged appearance": [ + "HP:0007495" + ], + "precociously senile appearance": [ + "HP:0007495" + ], + "focal friction - related palmoplantar hyperkeratosis": [ + "HP:0007497" + ], + "hyperkeratosis , palmoplantar , focal friction - related": [ + "HP:0007497" + ], + "recurrent staphylococcal infection": [ + "HP:0007499" + ], + "recurrent staphylococcal infections": [ + "HP:0007499" + ], + "decreased number of sweat gland": [ + "HP:0007500" + ], + "decreased number of sweat glands": [ + "HP:0007500" + ], + "decrease sweat gland": [ + "HP:0007500" + ], + "decreased sweat glands": [ + "HP:0007500" + ], + "decrease sweat pore": [ + "HP:0007500" + ], + "decreased sweat pores": [ + "HP:0007500" + ], + "streak of hyperkeratosis along each finger onto the palm": [ + "HP:0007501" + ], + "streaks of hyperkeratosis along each finger onto the palm": [ + "HP:0007501" + ], + "follicular hyperkeratosis": [ + "HP:0007502" + ], + "hyperkeratosis follicularis": [ + "HP:0007502" + ], + "generalize ichthyosis": [ + "HP:0007503" + ], + "generalized ichthyosis": [ + "HP:0007503" + ], + "generalise ichthyosis": [ + "HP:0007503" + ], + "generalised ichthyosis": [ + "HP:0007503" + ], + "diffuse slow skin atrophy": [ + "HP:0007504" + ], + "progressive hyperpigmentation": [ + "HP:0007505" + ], + "congenital absence of skin of limb": [ + "HP:0007506" + ], + "congenital absence of skin of limbs": [ + "HP:0007506" + ], + "miss skin on limb since birth": [ + "HP:0007506" + ], + "missing skin on limbs since birth": [ + "HP:0007506" + ], + "punctate palmar hyperkeratosis": [ + "HP:0007508" + ], + "patchy hypo - and hyperpigmentation": [ + "HP:0007509" + ], + "patchy hypo - and hyper - pigmentation": [ + "HP:0007509" + ], + "focal dermal aplasia / hypoplasia": [ + "HP:0007510" + ], + "mottle pigmentation of photoexposed area": [ + "HP:0007511" + ], + "mottled pigmentation of photoexposed areas": [ + "HP:0007511" + ], + "generalize hypopigmentation": [ + "HP:0007513" + ], + "generalized hypopigmentation": [ + "HP:0007513" + ], + "fair skin": [ + "HP:0007513" + ], + "generalise hypopigmentation": [ + "HP:0007513" + ], + "generalised hypopigmentation": [ + "HP:0007513" + ], + "pale pigmentation": [ + "HP:0007513" + ], + "edema of the dorsum of hand": [ + "HP:0007514" + ], + "edema of the dorsum of hands": [ + "HP:0007514" + ], + "edema of dorsum of hand": [ + "HP:0007514" + ], + "edema of dorsum of hands": [ + "HP:0007514" + ], + "oedema of dorsum of hand": [ + "HP:0007514" + ], + "oedema of dorsum of hands": [ + "HP:0007514" + ], + "oedema of the dorsum of hand": [ + "HP:0007514" + ], + "oedema of the dorsum of hands": [ + "HP:0007514" + ], + "hypoplastic pilosebaceous unit": [ + "HP:0007515" + ], + "hypoplastic pilosebaceous units": [ + "HP:0007515" + ], + "redundant skin on finger": [ + "HP:0007516" + ], + "redundant skin on fingers": [ + "HP:0007516" + ], + "extra skin on finger": [ + "HP:0007516" + ], + "extra skin on fingers": [ + "HP:0007516" + ], + "palmoplantar cutis laxa": [ + "HP:0007517" + ], + "excessive wrinkle skin of palm and sol": [ + "HP:0007517" + ], + "excessive wrinkled skin of palms and soles": [ + "HP:0007517" + ], + "furrow palm and sol": [ + "HP:0007517" + ], + "furrowed palms and soles": [ + "HP:0007517" + ], + "increased wrinkle of palm and sol": [ + "HP:0007517" + ], + "increased wrinkles of palms and soles": [ + "HP:0007517" + ], + "wrinkle palm and sol": [ + "HP:0007517" + ], + "wrinkled palms and soles": [ + "HP:0007517" + ], + "wrinkled skin of hand and foot": [ + "HP:0007517" + ], + "wrinkled skin of hands and feet": [ + "HP:0007517" + ], + "obsolete lack of subcutaneous fatty tissue": [ + "HP:0007519" + ], + "irregular hyperpigmentation of back": [ + "HP:0007521" + ], + "increased number of skin fold": [ + "HP:0007522" + ], + "increased number of skin folds": [ + "HP:0007522" + ], + "atypical neurofibromatosis": [ + "HP:0007524" + ], + "yellow subcutaneous tissue cover by thin , scaly skin": [ + "HP:0007525" + ], + "yellow subcutaneous tissue covered by thin , scaly skin": [ + "HP:0007525" + ], + "hypopigmented skin patch on arm": [ + "HP:0007526" + ], + "hypopigmented skin patches on arms": [ + "HP:0007526" + ], + "patchy loss of skin color on arm": [ + "HP:0007526" + ], + "patchy loss of skin color on arms": [ + "HP:0007526" + ], + "patchy loss of skin colour on arm": [ + "HP:0007526" + ], + "patchy loss of skin colour on arms": [ + "HP:0007526" + ], + "hidrotic ectodermal dysplasia": [ + "HP:0007529" + ], + "punctate palmoplantar hyperkeratosis": [ + "HP:0007530" + ], + "congenital posterior occipital alopecia": [ + "HP:0007534" + ], + "hypopigmented streak": [ + "HP:0007535" + ], + "hypopigmented streaks": [ + "HP:0007535" + ], + "aplasia cutis congenita of midline scalp vertex": [ + "HP:0007536" + ], + "severe photosensitivity": [ + "HP:0007537" + ], + "severe sun sensitivity": [ + "HP:0007537" + ], + "frontal cutaneous lipoma": [ + "HP:0007541" + ], + "absent pigmentation of the ventral chest": [ + "HP:0007542" + ], + "epidermal hyperkeratosis": [ + "HP:0007543" + ], + "increased thickness of skin epidermis": [ + "HP:0007543" + ], + "piebaldism": [ + "HP:0007544" + ], + "congenital palmoplantar hyperkeratosis": [ + "HP:0007545" + ], + "congenital palmoplantar keratoderma": [ + "HP:0007545" + ], + "congenital palmoplantar keratodermia": [ + "HP:0007545" + ], + "congenital palmoplantar keratosis": [ + "HP:0007545" + ], + "linear hyperpigmentation": [ + "HP:0007546" + ], + "palmoplantar keratosis with erythema and scale": [ + "HP:0007548" + ], + "desquamation of skin soon after birth": [ + "HP:0007549" + ], + "hypohidrosis or hyperhidrosis": [ + "HP:0007550" + ], + "lack of sweating or excessive sweating": [ + "HP:0007550" + ], + "abnormal subcutaneous fat tissue distribution": [ + "HP:0007552" + ], + "abnormal fat tissue distribution below the skin": [ + "HP:0007552" + ], + "congenital symmetrical palmoplantar keratosis": [ + "HP:0007553" + ], + "confetti hypopigmentation pattern of low leg skin": [ + "HP:0007554" + ], + "confetti hypopigmentation pattern of lower leg skin": [ + "HP:0007554" + ], + "plantar hyperkeratosis": [ + "HP:0007556" + ], + "plantar hyperkeratoses": [ + "HP:0007556" + ], + "localize epidermolytic hyperkeratosis": [ + "HP:0007559" + ], + "localized epidermolytic hyperkeratosis": [ + "HP:0007559" + ], + "localise epidermolytic hyperkeratosis": [ + "HP:0007559" + ], + "localised epidermolytic hyperkeratosis": [ + "HP:0007559" + ], + "unusual dermatoglyphic": [ + "HP:0007560" + ], + "unusual dermatoglyphics": [ + "HP:0007560" + ], + "telangiectases in sun - expose and nonexposed skin": [ + "HP:0007561" + ], + "telangiectases in sun - exposed and nonexposed skin": [ + "HP:0007561" + ], + "multiple cafe - au - lait spot": [ + "HP:0007565" + ], + "multiple cafe - au - lait spots": [ + "HP:0007565" + ], + "multiple birthmark": [ + "HP:0007565" + ], + "multiple birthmarks": [ + "HP:0007565" + ], + "multiple flat light - brown mark on skin": [ + "HP:0007565" + ], + "multiple flat light - brown marks on skin": [ + "HP:0007565" + ], + "index finger dermatoglyphic radial loop": [ + "HP:0007566" + ], + "generalize seborrheic dermatitis": [ + "HP:0007569" + ], + "generalized seborrheic dermatitis": [ + "HP:0007569" + ], + "generalise seborrheic dermatitis": [ + "HP:0007569" + ], + "generalised seborrheic dermatitis": [ + "HP:0007569" + ], + "generalise seborrheic eczema": [ + "HP:0007569" + ], + "generalised seborrheic eczema": [ + "HP:0007569" + ], + "generalize seborrheic eczema": [ + "HP:0007569" + ], + "generalized seborrheic eczema": [ + "HP:0007569" + ], + "hyperkeratosis lenticularis perstans": [ + "HP:0007570" + ], + "flegel disease": [ + "HP:0007570" + ], + "hyperpigmented streak": [ + "HP:0007572" + ], + "hyperpigmented streaks": [ + "HP:0007572" + ], + "late onset atopic dermatitis": [ + "HP:0007573" + ], + "late onset baby eczema": [ + "HP:0007573" + ], + "generalize bronze hyperpigmentation": [ + "HP:0007574" + ], + "generalized bronze hyperpigmentation": [ + "HP:0007574" + ], + "bronze skin": [ + "HP:0007574" + ], + "generalise bronze hyperpigmentation": [ + "HP:0007574" + ], + "generalised bronze hyperpigmentation": [ + "HP:0007574" + ], + "palmar neurofibroma": [ + "HP:0007576" + ], + "palmar neurofibromas": [ + "HP:0007576" + ], + "mediosternal , longitudinal streak of hypopigmentation": [ + "HP:0007581" + ], + "telangiectasia macularis eruptiva perstans": [ + "HP:0007583" + ], + "skin fragility with non - scarring blistering": [ + "HP:0007585" + ], + "telangiectases produce 'marbled ' skin": [ + "HP:0007586" + ], + "telangiectases producing 'marbled ' skin": [ + "HP:0007586" + ], + "numerous pigment freckle": [ + "HP:0007587" + ], + "numerous pigmented freckles": [ + "HP:0007587" + ], + "reticular hyperpigmentation": [ + "HP:0007588" + ], + "reticulate hyperpigmentation": [ + "HP:0007588" + ], + "aplasia cutis congenita on trunk or limb": [ + "HP:0007589" + ], + "aplasia cutis congenita on trunk or limbs": [ + "HP:0007589" + ], + "aplasia cutis congenita over posterior parietal area": [ + "HP:0007590" + ], + "aplasia / hypoplastia of the eccrine sweat gland": [ + "HP:0007592" + ], + "aplasia / hypoplastia of the eccrine sweat glands": [ + "HP:0007592" + ], + "hypoplastic - absent eccrine sweat gland": [ + "HP:0007592" + ], + "hypoplastic - absent eccrine sweat glands": [ + "HP:0007592" + ], + "redundant skin in infancy": [ + "HP:0007595" + ], + "excess skin in infancy": [ + "HP:0007595" + ], + "painful subcutaneous lipoma": [ + "HP:0007596" + ], + "painful subcutaneous lipomas": [ + "HP:0007596" + ], + "painful noncancerous fat tissue tumor under the skin": [ + "HP:0007596" + ], + "painful noncancerous fat tissue tumour under the skin": [ + "HP:0007596" + ], + "obsolete congenital palmoplantar keratodermia": [ + "HP:0007597" + ], + "bilateral single transverse palmar crease": [ + "HP:0007598" + ], + "bilateral single transverse palmar creases": [ + "HP:0007598" + ], + "generalize reticulate brown pigmentation": [ + "HP:0007599" + ], + "generalized reticulate brown pigmentation": [ + "HP:0007599" + ], + "generalise reticulate brown pigmentation": [ + "HP:0007599" + ], + "generalised reticulate brown pigmentation": [ + "HP:0007599" + ], + "midline facial capillary hemangioma": [ + "HP:0007601" + ], + "complex palmar dermatoglyphic pattern": [ + "HP:0007602" + ], + "freckle in sun - expose area": [ + "HP:0007603" + ], + "freckles in sun - exposed areas": [ + "HP:0007603" + ], + "excessive wrinkling of palmar skin": [ + "HP:0007605" + ], + "redundant , wrinkle skin of palm": [ + "HP:0007605" + ], + "redundant , wrinkled skin of palms": [ + "HP:0007605" + ], + "multiple cutaneous malignancy": [ + "HP:0007606" + ], + "multiple cutaneous malignancies": [ + "HP:0007606" + ], + "hypohidrotic ectodermal dysplasia": [ + "HP:0007607" + ], + "abnormal palmar dermal ridge": [ + "HP:0007608" + ], + "abnormal palmar dermal ridges": [ + "HP:0007608" + ], + "hypoproteinemic edema": [ + "HP:0007609" + ], + "hypoproteinemic oedema": [ + "HP:0007609" + ], + "blotch pigmentation of the skin": [ + "HP:0007610" + ], + "blotching pigmentation of the skin": [ + "HP:0007610" + ], + "spinous keratoses of palm and sol": [ + "HP:0007613" + ], + "spinous keratoses of palms and soles": [ + "HP:0007613" + ], + "nevus flammeus nucha": [ + "HP:0007616" + ], + "nevus flammeus nuchae": [ + "HP:0007616" + ], + "angel 's kiss": [ + "HP:0007616" + ], + "port - wine stain on neck": [ + "HP:0007616" + ], + "salmon patch": [ + "HP:0007616" + ], + "stork bite": [ + "HP:0007616" + ], + "fine , reticulate skin pigmentation": [ + "HP:0007617" + ], + "subcutaneous calcification": [ + "HP:0007618" + ], + "skin calcification": [ + "HP:0007618" + ], + "cutaneous leiomyoma": [ + "HP:0007620" + ], + "cutaneous leiomyomas": [ + "HP:0007620" + ], + "cutaneous leiomyomata": [ + "HP:0007620" + ], + "telangiectasia of extensor surface": [ + "HP:0007621" + ], + "telangiectasia of extensor surfaces": [ + "HP:0007621" + ], + "pigmentation anomaly of sun - expose skin": [ + "HP:0007623" + ], + "pigmentation anomalies of sun - exposed skin": [ + "HP:0007623" + ], + "abnormal pigmentation in sun - expose skin": [ + "HP:0007623" + ], + "abnormal pigmentation in sun - exposed skin": [ + "HP:0007623" + ], + "mandibular osteomyelitis": [ + "HP:0007626" + ], + "low jaw bone infection": [ + "HP:0007626" + ], + "lower jaw bone infection": [ + "HP:0007626" + ], + "osteomyelitis , especially of the mandible": [ + "HP:0007626" + ], + "mandibular condyle aplasia": [ + "HP:0007627" + ], + "absence of the condylar head of mandible": [ + "HP:0007627" + ], + "absence of the condylar neck of mandible": [ + "HP:0007627" + ], + "absence of the condylar process of mandible": [ + "HP:0007627" + ], + "agenesis of condylar head of mandible": [ + "HP:0007627" + ], + "agenesis of condylar neck of mandible": [ + "HP:0007627" + ], + "agenesis of condylar process of mandible": [ + "HP:0007627" + ], + "failure of development of condylar head of mandible": [ + "HP:0007627" + ], + "failure of development of condylar neck of mandible": [ + "HP:0007627" + ], + "failure of development of the condylar process of mandible": [ + "HP:0007627" + ], + "underdevelopment of condylar head of mandible": [ + "HP:0007627" + ], + "underdevelopment of condylar neck of mandible": [ + "HP:0007627" + ], + "underdevelopment of condylar process of mandible": [ + "HP:0007627" + ], + "mandibular condyle hypoplasia": [ + "HP:0007628" + ], + "decreased size of condylar process of mandible": [ + "HP:0007628" + ], + "decreased size of mandibular condyle": [ + "HP:0007628" + ], + "hypoplasia of condylar head of mandible": [ + "HP:0007628" + ], + "hypoplasia of condylar neck of mandible": [ + "HP:0007628" + ], + "hypoplasia of condylar process of mandible": [ + "HP:0007628" + ], + "hypoplasia of mandibular condyle": [ + "HP:0007628" + ], + "hypoplasia of subcondylar region of mandible": [ + "HP:0007628" + ], + "hypotrophic condylar process of mandible": [ + "HP:0007628" + ], + "hypotrophic mandibular condyle": [ + "HP:0007628" + ], + "small condylar head of mandible": [ + "HP:0007628" + ], + "small condylar neck of mandible": [ + "HP:0007628" + ], + "small mandibular condyle": [ + "HP:0007628" + ], + "bilateral microphthalmos": [ + "HP:0007633" + ], + "abnormally small eyeball on both side": [ + "HP:0007633" + ], + "abnormally small eyeball on both sides": [ + "HP:0007633" + ], + "bilateral nanophthalmos": [ + "HP:0007633" + ], + "decreased size of eyeballs": [ + "HP:0007633" + ], + "decreased size of globes of eyes": [ + "HP:0007633" + ], + "microphthalmia , bilateral": [ + "HP:0007633" + ], + "nonarteritic anterior ischemic optic neuropathy": [ + "HP:0007634" + ], + "nonarteritic anterior ischaemic optic neuropathy": [ + "HP:0007634" + ], + "dyschromatopsia": [ + "HP:0007641" + ], + "color blindness": [ + "HP:0007641" + ], + "colour blindness": [ + "HP:0007641" + ], + "congenital stationary night blindness": [ + "HP:0007642" + ], + "congenital night blindness": [ + "HP:0007642" + ], + "night blindness since birth": [ + "HP:0007642" + ], + "night blindness , congenital": [ + "HP:0007642" + ], + "night blindness , congenital stationary": [ + "HP:0007642" + ], + "night blindness , congenital stationary , complete": [ + "HP:0007642" + ], + "night blindness , stationary": [ + "HP:0007642" + ], + "static congenital hemeralopia": [ + "HP:0007642" + ], + "peripheral tractional retinal detachment": [ + "HP:0007643" + ], + "peripheral traction retinal detachment": [ + "HP:0007643" + ], + "tractional retinal detachment at the periphery of the retina": [ + "HP:0007643" + ], + "absent low eyelash": [ + "HP:0007646" + ], + "absent lower eyelashes": [ + "HP:0007646" + ], + "agenesis of low eyelash": [ + "HP:0007646" + ], + "agenesis of lower eyelashes": [ + "HP:0007646" + ], + "aplasia of low eyelash": [ + "HP:0007646" + ], + "aplasia of lower eyelashes": [ + "HP:0007646" + ], + "atrichia of low eyelash": [ + "HP:0007646" + ], + "atrichia of lower eyelashes": [ + "HP:0007646" + ], + "failure of development of low eyelash": [ + "HP:0007646" + ], + "failure of development of lower eyelashes": [ + "HP:0007646" + ], + "congenital extraocular muscle anomaly": [ + "HP:0007647" + ], + "punctate cataract": [ + "HP:0007648" + ], + "punctate lenticular opacity": [ + "HP:0007648" + ], + "punctate lenticular opacities": [ + "HP:0007648" + ], + "congenital hypertrophy of retinal pigment epithelium": [ + "HP:0007649" + ], + "progressive ophthalmoplegia": [ + "HP:0007650" + ], + "ectropion of low eyelid": [ + "HP:0007651" + ], + "ectropion of lower eyelids": [ + "HP:0007651" + ], + "evert low eyelid": [ + "HP:0007651" + ], + "everted lower eyelids": [ + "HP:0007651" + ], + "low eyelid fold out": [ + "HP:0007651" + ], + "lower eyelid folded out": [ + "HP:0007651" + ], + "low eyelid turn out": [ + "HP:0007651" + ], + "lower eyelid turned out": [ + "HP:0007651" + ], + "obsolete retinal striation": [ + "HP:0007654" + ], + "eversion of lateral third of low eyelid": [ + "HP:0007655" + ], + "eversion of lateral third of lower eyelids": [ + "HP:0007655" + ], + "lacrimal gland aplasia": [ + "HP:0007656" + ], + "absent tear gland": [ + "HP:0007656" + ], + "diffuse nuclear cataract": [ + "HP:0007657" + ], + "large hyperpigmented retinal spot": [ + "HP:0007658" + ], + "large hyperpigmented retinal spots": [ + "HP:0007658" + ], + "obsolete decrease retinal pigmentation with dispersion": [ + "HP:0007659" + ], + "obsolete decreased retinal pigmentation with dispersion": [ + "HP:0007659" + ], + "abnormality of chorioretinal pigmentation": [ + "HP:0007661" + ], + "reduce visual acuity": [ + "HP:0007663" + ], + "reduced visual acuity": [ + "HP:0007663" + ], + "decreased central vision": [ + "HP:0007663" + ], + "decreased clarity of vision": [ + "HP:0007663" + ], + "decrease visual acuity": [ + "HP:0007663" + ], + "decreased visual acuity": [ + "HP:0007663" + ], + "poor visual acuity": [ + "HP:0007663" + ], + "curly eyelash": [ + "HP:0007665" + ], + "curly eyelashes": [ + "HP:0007665" + ], + "peripheral cystoid retinal degeneration": [ + "HP:0007667" + ], + "cystic retinal degeneration": [ + "HP:0007667" + ], + "peripheral cystoid degeneration": [ + "HP:0007667" + ], + "impaired pursuit initiation and maintenance": [ + "HP:0007668" + ], + "abnormal vestibulo - ocular reflex": [ + "HP:0007670" + ], + "abnormal vestibuloocular reflex": [ + "HP:0007670" + ], + "progressive night blindness": [ + "HP:0007675" + ], + "hypoplasia of the iris": [ + "HP:0007676" + ], + "hypoplastic iris": [ + "HP:0007676" + ], + "iris hypoplasia": [ + "HP:0007676" + ], + "underdeveloped iris": [ + "HP:0007676" + ], + "vitelliform - like macular lesion": [ + "HP:0007677" + ], + "vitelliform - like macular lesions": [ + "HP:0007677" + ], + "vitelliform macular dystrophy": [ + "HP:0007677" + ], + "vitelliform macular lesion": [ + "HP:0007677" + ], + "vitelliform macular lesions": [ + "HP:0007677" + ], + "lacrimal duct stenosis": [ + "HP:0007678" + ], + "narrowing of the tear duct": [ + "HP:0007678" + ], + "nasolacrimal duct stenosis": [ + "HP:0007678" + ], + "depigmented fundus": [ + "HP:0007680" + ], + "peripheral retinal avascularization": [ + "HP:0007685" + ], + "abnormal pupillary function": [ + "HP:0007686" + ], + "unilateral ptosis": [ + "HP:0007687" + ], + "dropping of one upper eyelid": [ + "HP:0007687" + ], + "undetectable light - and dark - adapt electroretinogram": [ + "HP:0007688" + ], + "undetectable light - and dark - adapted electroretinogram": [ + "HP:0007688" + ], + "absent cone and rod function by electroretinogram": [ + "HP:0007688" + ], + "absent cone and rod functions by electroretinogram": [ + "HP:0007688" + ], + "absent rod - and cone - mediate response on erg": [ + "HP:0007688" + ], + "absent rod - and cone - mediated responses on erg": [ + "HP:0007688" + ], + "map - dot - fingerprint corneal dystrophy": [ + "HP:0007690" + ], + "obsolete short curly eyelash": [ + "HP:0007691" + ], + "obsolete short curly eyelashes": [ + "HP:0007691" + ], + "obsolete nonnuclear polymorphic congenital cataract": [ + "HP:0007692" + ], + "abnormal pupillary light reflex": [ + "HP:0007695" + ], + "hypoplasia of the low eyelid": [ + "HP:0007697" + ], + "hypoplasia of the lower eyelids": [ + "HP:0007697" + ], + "decreased size of low eyelid": [ + "HP:0007697" + ], + "decreased size of lower eyelid": [ + "HP:0007697" + ], + "hypotrophic low eyelid": [ + "HP:0007697" + ], + "hypotrophic lower eyelid": [ + "HP:0007697" + ], + "short low eyelid": [ + "HP:0007697" + ], + "short lower eyelid": [ + "HP:0007697" + ], + "small low eyelid": [ + "HP:0007697" + ], + "small lower eyelid": [ + "HP:0007697" + ], + "underdevelopment of low eyelid": [ + "HP:0007697" + ], + "underdevelopment of lower eyelid": [ + "HP:0007697" + ], + "obsolete retinal pigment epithelial atrophy": [ + "HP:0007698" + ], + "ocular anterior segment dysgenesis": [ + "HP:0007700" + ], + "anterior chamber cleavage defect": [ + "HP:0007700" + ], + "anterior chamber cleavage disorder": [ + "HP:0007700" + ], + "anterior chamber malformation": [ + "HP:0007700" + ], + "anterior chamber mesodermal anomaly": [ + "HP:0007700" + ], + "anterior chamber mesodermal anomalies": [ + "HP:0007700" + ], + "anterior segment developmental abnormality": [ + "HP:0007700" + ], + "anterior segment dysgenesis": [ + "HP:0007700" + ], + "anterior segment mesencyhmal dysgenesis": [ + "HP:0007700" + ], + "anterior segment ocular dysgenesis": [ + "HP:0007700" + ], + "obsolete pigmentary retinal deposit": [ + "HP:0007702" + ], + "obsolete pigmentary retinal deposits": [ + "HP:0007702" + ], + "abnormality of retinal pigmentation": [ + "HP:0007703" + ], + "abnormal retinal pigmentation": [ + "HP:0007703" + ], + "abnormality of retinal pigment epithelium": [ + "HP:0007703" + ], + "abnormality of rpe": [ + "HP:0007703" + ], + "abnormality of the retinal pigment epithelium": [ + "HP:0007703" + ], + "retinal pigmentary anomaly": [ + "HP:0007703" + ], + "paroxysmal involuntary eye movement": [ + "HP:0007704" + ], + "paroxysmal involuntary eye movements": [ + "HP:0007704" + ], + "abnormal eye movement , paroxysmal": [ + "HP:0007704" + ], + "abnormal eye movements , paroxysmal": [ + "HP:0007704" + ], + "corneal degeneration": [ + "HP:0007705" + ], + "congenital aphakia": [ + "HP:0007707" + ], + "lens agenesis": [ + "HP:0007707" + ], + "absent inner eyelash": [ + "HP:0007708" + ], + "absent inner eyelashes": [ + "HP:0007708" + ], + "band - shaped corneal dystrophy": [ + "HP:0007709" + ], + "peripheral vitreous opacity": [ + "HP:0007710" + ], + "peripheral vitreous opacities": [ + "HP:0007710" + ], + "obsolete choroidal dystrophy": [ + "HP:0007712" + ], + "obsolete juvenile zonular cataract": [ + "HP:0007713" + ], + "obsolete juvenile zonular cataracts": [ + "HP:0007713" + ], + "weak extraocular muscle": [ + "HP:0007715" + ], + "weak extraocular muscles": [ + "HP:0007715" + ], + "uveal melanoma": [ + "HP:0007716" + ], + "intraocular melanoma": [ + "HP:0007716" + ], + "chronic irritative conjunctivitis": [ + "HP:0007717" + ], + "flat cornea": [ + "HP:0007720" + ], + "cornea plana": [ + "HP:0007720" + ], + "saccular conjunctival dilatation": [ + "HP:0007721" + ], + "saccular conjunctival dilatations": [ + "HP:0007721" + ], + "saccular conjunctival aneurysm": [ + "HP:0007721" + ], + "saccular conjunctival aneurysms": [ + "HP:0007721" + ], + "retinal pigment epithelial atrophy": [ + "HP:0007722" + ], + "opacification of the corneal epithelium": [ + "HP:0007727" + ], + "superficial corneal opacity": [ + "HP:0007727" + ], + "superficial corneal opacities": [ + "HP:0007727" + ], + "congenital miosis": [ + "HP:0007728" + ], + "iris hypopigmentation": [ + "HP:0007730" + ], + "light eye color": [ + "HP:0007730" + ], + "light eye colour": [ + "HP:0007730" + ], + "reduce iris pigmentation": [ + "HP:0007730" + ], + "reduced iris pigmentation": [ + "HP:0007730" + ], + "chorioretinal dysplasia": [ + "HP:0007731" + ], + "lacrimal gland hypoplasia": [ + "HP:0007732" + ], + "hypoplastic lacrimal gland": [ + "HP:0007732" + ], + "underdeveloped tear gland": [ + "HP:0007732" + ], + "laterally curve eyebrow": [ + "HP:0007733" + ], + "laterally curved eyebrow": [ + "HP:0007733" + ], + "enlarge lacrimal gland": [ + "HP:0007734" + ], + "enlarged lacrimal glands": [ + "HP:0007734" + ], + "enlarge tear gland": [ + "HP:0007734" + ], + "enlarged tear gland": [ + "HP:0007734" + ], + "obsolete pericentral retinal dystrophy": [ + "HP:0007736" + ], + "bone spicule pigmentation of the retina": [ + "HP:0007737" + ], + "bone corpuscle fundus pigmentation": [ + "HP:0007737" + ], + "fundus with peripheral bony spicule": [ + "HP:0007737" + ], + "fundus with peripheral bony spicules": [ + "HP:0007737" + ], + "retinal 'bone corpuscle ' pigmentation": [ + "HP:0007737" + ], + "retinal bone corpuscle pigmentation": [ + "HP:0007737" + ], + "retinal pigment bone spicule": [ + "HP:0007737" + ], + "retinal pigmented bone spicules": [ + "HP:0007737" + ], + "uncontrolled eye movement": [ + "HP:0007738" + ], + "uncontrolled eye movements": [ + "HP:0007738" + ], + "obsolete mildly reduce visual acuity": [ + "HP:0007739" + ], + "obsolete mildly reduced visual acuity": [ + "HP:0007739" + ], + "long eyelash in irregular row": [ + "HP:0007740" + ], + "long eyelashes in irregular rows": [ + "HP:0007740" + ], + "obsolete iridoretinal coloboma": [ + "HP:0007744" + ], + "monocular horizontal nystagmus": [ + "HP:0007747" + ], + "obsolete irido - fundal coloboma": [ + "HP:0007748" + ], + "hypoplasia of the fovea": [ + "HP:0007750" + ], + "dull foveal reflex": [ + "HP:0007750" + ], + "foveal hypoplasia": [ + "HP:0007750" + ], + "macular dystrophy": [ + "HP:0007754" + ], + "juvenile epithelial corneal dystrophy": [ + "HP:0007755" + ], + "obsolete slitlike anterior chamber angle in child": [ + "HP:0007756" + ], + "obsolete slitlike anterior chamber angles in children": [ + "HP:0007756" + ], + "obsolete hypoplasia of choroid": [ + "HP:0007757" + ], + "obsolete congenital visual impairment": [ + "HP:0007758" + ], + "opacification of the corneal stroma": [ + "HP:0007759" + ], + "cloudy cornea": [ + "HP:0007759" + ], + "cloudy corneas": [ + "HP:0007759" + ], + "corneal stromal opacity": [ + "HP:0007759" + ], + "crystalline corneal dystrophy": [ + "HP:0007760" + ], + "pericentral scotoma": [ + "HP:0007761" + ], + "retinal telangiectasia": [ + "HP:0007763" + ], + "deep anterior chamber": [ + "HP:0007765" + ], + "optic disc hypoplasia": [ + "HP:0007766" + ], + "hypoplastic optic disc": [ + "HP:0007766" + ], + "hypoplastic optic discs": [ + "HP:0007766" + ], + "hypoplastic optic disk": [ + "HP:0007766" + ], + "hypoplastic optic disks": [ + "HP:0007766" + ], + "central retinal vessel vascular tortuosity": [ + "HP:0007768" + ], + "tortuosity of main retinal vessel": [ + "HP:0007768" + ], + "tortuosity of main retinal vessels": [ + "HP:0007768" + ], + "peripheral retinal degeneration": [ + "HP:0007769" + ], + "hypoplasia of the retina": [ + "HP:0007770" + ], + "retinal hypoplasia": [ + "HP:0007770" + ], + "underdeveloped retina": [ + "HP:0007770" + ], + "impaired smooth pursuit": [ + "HP:0007772" + ], + "abnormal visual pursuit": [ + "HP:0007772" + ], + "abnormality of visual tracking": [ + "HP:0007772" + ], + "impairment of visual pursuit": [ + "HP:0007772" + ], + "vitreoretinopathy": [ + "HP:0007773" + ], + "vitreoretinal abnormality": [ + "HP:0007773" + ], + "vitreoretinal degeneration": [ + "HP:0007773" + ], + "hypoplasia of the ciliary body": [ + "HP:0007774" + ], + "sparse lower eyelash": [ + "HP:0007776" + ], + "sparse lower eyelashes": [ + "HP:0007776" + ], + "hypotrichosis of low eyelash": [ + "HP:0007776" + ], + "hypotrichosis of lower eyelashes": [ + "HP:0007776" + ], + "partial absence of low eyelash": [ + "HP:0007776" + ], + "partial absence of lower eyelashes": [ + "HP:0007776" + ], + "scanty lower eyelash": [ + "HP:0007776" + ], + "scanty lower eyelashes": [ + "HP:0007776" + ], + "thin low eyelash": [ + "HP:0007776" + ], + "thin lower eyelashes": [ + "HP:0007776" + ], + "chorioretinal scar": [ + "HP:0007777" + ], + "posterior retinal neovascularization": [ + "HP:0007778" + ], + "neovascularization of peripheral and posterior retina": [ + "HP:0007778" + ], + "posterior retinal neovascularisation": [ + "HP:0007778" + ], + "anterior segment of eye aplasia": [ + "HP:0007779" + ], + "cortical pulverulent cataract": [ + "HP:0007780" + ], + "cataract , cortical pulverulent": [ + "HP:0007780" + ], + "cataracts , cortical pulverulent": [ + "HP:0007780" + ], + "obsolete peripheral retinal cone degeneration": [ + "HP:0007782" + ], + "obsolete butterfly retinal pigment epithelial dystrophy": [ + "HP:0007783" + ], + "obsolete lacunar retinal depigmentation": [ + "HP:0007786" + ], + "posterior subcapsular cataract": [ + "HP:0007787" + ], + "posterior subcapsular cataracts": [ + "HP:0007787" + ], + "posterior subcapsular opacity of the lens": [ + "HP:0007787" + ], + "posterior subcapsular opacities of the lens": [ + "HP:0007787" + ], + "patchy atrophy of the retinal pigment epithelium": [ + "HP:0007791" + ], + "microsaccadic pursuit": [ + "HP:0007792" + ], + "granular macular appearance": [ + "HP:0007793" + ], + "macular retinal pigment epithelial mottling": [ + "HP:0007793" + ], + "anterior cortical cataract": [ + "HP:0007795" + ], + "retinal vascular malformation": [ + "HP:0007797" + ], + "obsolete foveal dystrophy": [ + "HP:0007798" + ], + "conjunctival whitish salt - like deposit": [ + "HP:0007799" + ], + "conjunctival whitish salt - like deposits": [ + "HP:0007799" + ], + "increase axial length of the globe": [ + "HP:0007800" + ], + "increased axial length of the globe": [ + "HP:0007800" + ], + "globe elongate": [ + "HP:0007800" + ], + "globe elongated": [ + "HP:0007800" + ], + "increase axial globe length": [ + "HP:0007800" + ], + "increased axial globe length": [ + "HP:0007800" + ], + "increase front to back length of eyeball": [ + "HP:0007800" + ], + "increased front to back length of eyeball": [ + "HP:0007800" + ], + "obsolete fishnet retinal pigmentation": [ + "HP:0007801" + ], + "granular corneal dystrophy": [ + "HP:0007802" + ], + "monochromacy": [ + "HP:0007803" + ], + "complete achromatopsia": [ + "HP:0007803" + ], + "total colorblindness": [ + "HP:0007803" + ], + "optic nerve compression": [ + "HP:0007807" + ], + "obsolete bilateral retinal coloboma": [ + "HP:0007808" + ], + "punctate corneal dystrophy": [ + "HP:0007809" + ], + "obsolete progressive bifocal chorioretinal atrophy": [ + "HP:0007810" + ], + "horizontal pendular nystagmus": [ + "HP:0007811" + ], + "herpetiform corneal ulceration": [ + "HP:0007812" + ], + "dendritic corneal epithelial ulcer": [ + "HP:0007812" + ], + "herpetiform corneal ulcer": [ + "HP:0007812" + ], + "herpetiform corneal ulcers": [ + "HP:0007812" + ], + "nongranulomatous uveitis": [ + "HP:0007813" + ], + "retinal pigment epithelial mottling": [ + "HP:0007814" + ], + "focal hypopigmentation of the retinal pigment epithelium": [ + "HP:0007814" + ], + "retinal pigment epithelium irregularity": [ + "HP:0007814" + ], + "rpe irregularity": [ + "HP:0007814" + ], + "rpe mottling": [ + "HP:0007814" + ], + "salt and pepper retinal pigmentation": [ + "HP:0007814" + ], + "salt and pepper retinopathy": [ + "HP:0007814" + ], + "abnormal distribution of retinal arteriole and venule": [ + "HP:0007815" + ], + "abnormal distribution of retinal arterioles and venules": [ + "HP:0007815" + ], + "horizontal supranuclear gaze palsy": [ + "HP:0007817" + ], + "central heterochromia": [ + "HP:0007818" + ], + "ring iris heterochromia": [ + "HP:0007818" + ], + "presenile cataract": [ + "HP:0007819" + ], + "presenile cataracts": [ + "HP:0007819" + ], + "lacrimal punctal atresia": [ + "HP:0007820" + ], + "atretic lacrimal puncta": [ + "HP:0007820" + ], + "atretic lacrimal punctum": [ + "HP:0007820" + ], + "central retinal exudate": [ + "HP:0007822" + ], + "total ophthalmoplegia": [ + "HP:0007824" + ], + "complete ophthalmoplegia": [ + "HP:0007824" + ], + "global paralysis of gaze": [ + "HP:0007824" + ], + "total internal and external ophthalmoplegia": [ + "HP:0007824" + ], + "obsolete cataract develop in second or third decade": [ + "HP:0007825" + ], + "obsolete cataracts develop in second or third decade": [ + "HP:0007825" + ], + "nodular corneal dystrophy": [ + "HP:0007827" + ], + "obsolete diffuse retinal cone degeneration": [ + "HP:0007829" + ], + "adult - onset night blindness": [ + "HP:0007830" + ], + "nonprogressive restrictive external ophthalmoplegia": [ + "HP:0007831" + ], + "pigmentation of the sclera": [ + "HP:0007832" + ], + "pigmentation of the outer white part of the eyeball": [ + "HP:0007832" + ], + "anterior chamber synechiae": [ + "HP:0007833" + ], + "progressive cataract": [ + "HP:0007834" + ], + "cataract , progressive": [ + "HP:0007834" + ], + "s - shaped palpebral fissure": [ + "HP:0007835" + ], + "s - shaped palpebral fissures": [ + "HP:0007835" + ], + "s - shaped eye": [ + "HP:0007835" + ], + "s - shaped eyes": [ + "HP:0007835" + ], + "s - shape open between the eyelid": [ + "HP:0007835" + ], + "s - shaped opening between the eyelids": [ + "HP:0007835" + ], + "mosaic corneal dystrophy": [ + "HP:0007836" + ], + "progressive ptosis": [ + "HP:0007838" + ], + "progressive drooping of upper eyelid": [ + "HP:0007838" + ], + "long upper eyelash": [ + "HP:0007840" + ], + "long upper eyelashes": [ + "HP:0007840" + ], + "ciliary trichomegaly of upper eyelash": [ + "HP:0007840" + ], + "ciliary trichomegaly of upper eyelashes": [ + "HP:0007840" + ], + "increased length of upper eyelash": [ + "HP:0007840" + ], + "increased length of upper eyelashes": [ + "HP:0007840" + ], + "amyloid deposition in the vitreous humor": [ + "HP:0007841" + ], + "amyloid deposition in the vitreous humour": [ + "HP:0007841" + ], + "vitreous amyloid deposit": [ + "HP:0007841" + ], + "vitreous amyloid deposits": [ + "HP:0007841" + ], + "attenuation of retinal blood vessel": [ + "HP:0007843" + ], + "attenuation of retinal blood vessels": [ + "HP:0007843" + ], + "narrowing of blood vessel in back of eye": [ + "HP:0007843" + ], + "narrowing of blood vessels in back of eye": [ + "HP:0007843" + ], + "retinal vascular proliferation": [ + "HP:0007850" + ], + "obsolete temporal displacement of macula": [ + "HP:0007851" + ], + "obsolete temporal displacement of maculae": [ + "HP:0007851" + ], + "obsolete pericentral pigmentary retinopathy": [ + "HP:0007852" + ], + "glaucomatous visual field defect": [ + "HP:0007854" + ], + "punctate opacification of the cornea": [ + "HP:0007856" + ], + "punctate corneal opacity": [ + "HP:0007856" + ], + "punctate corneal opacities": [ + "HP:0007856" + ], + "chorioretinal lacuna": [ + "HP:0007858" + ], + "chorioretinal lacunae": [ + "HP:0007858" + ], + "lacunar retinal depigmentation": [ + "HP:0007858" + ], + "congenital horizontal nystagmus": [ + "HP:0007859" + ], + "nystagmus , congenital horizontal": [ + "HP:0007859" + ], + "retinal calcification": [ + "HP:0007862" + ], + "retinal infarction": [ + "HP:0007866" + ], + "restrictive partial external ophthalmoplegia": [ + "HP:0007867" + ], + "obsolete age - related macular degeneration": [ + "HP:0007868" + ], + "obsolete peripheral retinopathy": [ + "HP:0007869" + ], + "choroidal hemangioma": [ + "HP:0007872" + ], + "abnormally prominent line of schwalbe": [ + "HP:0007873" + ], + "prominent schwalbe line": [ + "HP:0007873" + ], + "prominent schwalbe lines": [ + "HP:0007873" + ], + "almond - shaped palpebral fissure": [ + "HP:0007874" + ], + "almond shape eye": [ + "HP:0007874" + ], + "almond shaped eyes": [ + "HP:0007874" + ], + "almond - shape open between the eyelid": [ + "HP:0007874" + ], + "almond - shaped opening between the eyelids": [ + "HP:0007874" + ], + "congenital blindness": [ + "HP:0007875" + ], + "blindness present at birth": [ + "HP:0007875" + ], + "congenital amaurosis": [ + "HP:0007875" + ], + "obsolete juvenile cortical cataract": [ + "HP:0007876" + ], + "allergic conjunctivitis": [ + "HP:0007879" + ], + "marginal corneal dystrophy": [ + "HP:0007880" + ], + "central corneal dystrophy": [ + "HP:0007881" + ], + "slow horizontal saccade": [ + "HP:0007885" + ], + "slowed horizontal saccades": [ + "HP:0007885" + ], + "absent extraocular muscle": [ + "HP:0007886" + ], + "absent extraocular muscles": [ + "HP:0007886" + ], + "absent ocular muscle": [ + "HP:0007886" + ], + "absent ocular muscles": [ + "HP:0007886" + ], + "miss eye muscle": [ + "HP:0007886" + ], + "missing eye muscles": [ + "HP:0007886" + ], + "iridescent posterior subcapsular cataract": [ + "HP:0007889" + ], + "cataract , posterior , subcapsular , iridescent": [ + "HP:0007889" + ], + "cataracts , posterior , subcapsular , iridescent": [ + "HP:0007889" + ], + "hypoplasia of the lacrimal punctum": [ + "HP:0007892" + ], + "hypoplasia of the lacrimal puncta": [ + "HP:0007892" + ], + "hypoplastic lacrimal puncta": [ + "HP:0007892" + ], + "obsolete progressive retinal degeneration": [ + "HP:0007893" + ], + "hypopigmentation of the fundus": [ + "HP:0007894" + ], + "decrease fundus pigmentation": [ + "HP:0007894" + ], + "decreased fundus pigmentation": [ + "HP:0007894" + ], + "fundus hypopigmentation": [ + "HP:0007894" + ], + "exudative retinopathy": [ + "HP:0007898" + ], + "retinal nonattachment": [ + "HP:0007899" + ], + "congenital retinal non - attachment": [ + "HP:0007899" + ], + "hypoplastic lacrimal duct": [ + "HP:0007900" + ], + "underdeveloped tear duct": [ + "HP:0007900" + ], + "obsolete retinal malformation": [ + "HP:0007901" + ], + "vitreous hemorrhage": [ + "HP:0007902" + ], + "vitreous haemorrhage": [ + "HP:0007902" + ], + "paravenous chorioretinal atrophy": [ + "HP:0007903" + ], + "abnormal iris vasculature": [ + "HP:0007905" + ], + "abnormality of iris blood vessel": [ + "HP:0007905" + ], + "abnormality of iris blood vessels": [ + "HP:0007905" + ], + "ocular hypertension": [ + "HP:0007906" + ], + "elevate intraocular pressure": [ + "HP:0007906" + ], + "elevated intraocular pressure": [ + "HP:0007906" + ], + "elevate iop": [ + "HP:0007906" + ], + "elevated iop": [ + "HP:0007906" + ], + "high eye pressure": [ + "HP:0007906" + ], + "increase intraocular pressure": [ + "HP:0007906" + ], + "increased intraocular pressure": [ + "HP:0007906" + ], + "increase iop": [ + "HP:0007906" + ], + "increased iop": [ + "HP:0007906" + ], + "raise intraocular pressure": [ + "HP:0007906" + ], + "raised intraocular pressure": [ + "HP:0007906" + ], + "raise iop": [ + "HP:0007906" + ], + "raised iop": [ + "HP:0007906" + ], + "obsolete nonprogressive congenital retinal dystrophy": [ + "HP:0007910" + ], + "congenital bilateral ptosis": [ + "HP:0007911" + ], + "congenital drooping of both upper eyelid": [ + "HP:0007911" + ], + "congenital drooping of both upper eyelids": [ + "HP:0007911" + ], + "ptosis , bilateral congenital": [ + "HP:0007911" + ], + "ptosis , congenital bilateral": [ + "HP:0007911" + ], + "reticular retinal dystrophy": [ + "HP:0007913" + ], + "polymorphous posterior corneal dystrophy": [ + "HP:0007915" + ], + "obsolete small anterior lens surface opacity": [ + "HP:0007916" + ], + "obsolete small anterior lens surface opacities": [ + "HP:0007916" + ], + "tractional retinal detachment": [ + "HP:0007917" + ], + "obsolete congenital chorioretinal dystrophy": [ + "HP:0007920" + ], + "hypermyelinated retinal nerve fiber": [ + "HP:0007922" + ], + "hypermyelinated retinal nerve fibers": [ + "HP:0007922" + ], + "hypermyelinated retinal nerve fibre": [ + "HP:0007922" + ], + "hypermyelinated retinal nerve fibres": [ + "HP:0007922" + ], + "retinal striation": [ + "HP:0007922" + ], + "obsolete foveal hyperplasia": [ + "HP:0007923" + ], + "slow decrease in visual acuity": [ + "HP:0007924" + ], + "decrease visual acuity , slowly progressive": [ + "HP:0007924" + ], + "decreased visual acuity , slowly progressive": [ + "HP:0007924" + ], + "slow decrease in sharpness of vision": [ + "HP:0007924" + ], + "subacute deterioration of visual acuity": [ + "HP:0007924" + ], + "lacrimal duct aplasia": [ + "HP:0007925" + ], + "absent tear duct": [ + "HP:0007925" + ], + "abnormal flash visual evoke potential": [ + "HP:0007928" + ], + "abnormal flash visual evoked potentials": [ + "HP:0007928" + ], + "peripheral retinal detachment": [ + "HP:0007929" + ], + "obsolete prominent epicanthal fold": [ + "HP:0007930" + ], + "obsolete prominent epicanthal folds": [ + "HP:0007930" + ], + "bilateral congenital mydriasis": [ + "HP:0007932" + ], + "broad lateral eyebrow": [ + "HP:0007933" + ], + "wide lateral eyebrow": [ + "HP:0007933" + ], + "juvenile posterior subcapsular lenticular opacity": [ + "HP:0007935" + ], + "juvenile posterior subcapsular lenticular opacities": [ + "HP:0007935" + ], + "restrictive external ophthalmoplegia": [ + "HP:0007936" + ], + "restrictive external ophthalmoplegia , bilateral": [ + "HP:0007936" + ], + "restrictive ophthalmoplegia": [ + "HP:0007936" + ], + "reticular pigmentary degeneration": [ + "HP:0007937" + ], + "fishnet retinal pigmentation": [ + "HP:0007937" + ], + "honeycomb retinal degeneration": [ + "HP:0007937" + ], + "blue cone monochromacy": [ + "HP:0007939" + ], + "blue cone monochromatism": [ + "HP:0007939" + ], + "incomplete achromatopsia": [ + "HP:0007939" + ], + "s - cone monochromacy": [ + "HP:0007939" + ], + "limited extraocular movement": [ + "HP:0007941" + ], + "limited extraocular movements": [ + "HP:0007941" + ], + "internal ophthalmoplegia": [ + "HP:0007942" + ], + "congenital stapes ankylosis": [ + "HP:0007943" + ], + "intermittent microsaccadic pursuit": [ + "HP:0007944" + ], + "intermittent microsaccadic pursuits": [ + "HP:0007944" + ], + "obsolete choroidal degeneration": [ + "HP:0007945" + ], + "unilateral narrow palpebral fissure": [ + "HP:0007946" + ], + "narrow palpebral fissure , unilateral": [ + "HP:0007946" + ], + "unequal size of open between the eyelid": [ + "HP:0007946" + ], + "unequal size of opening between the eyelids": [ + "HP:0007946" + ], + "pericentral retinitis pigmentosa": [ + "HP:0007947" + ], + "dense posterior cortical cataract": [ + "HP:0007948" + ], + "obsolete progressive macular scarring": [ + "HP:0007949" + ], + "peripapillary chorioretinal atrophy": [ + "HP:0007950" + ], + "obsolete bilateral choroid coloboma": [ + "HP:0007956" + ], + "corneal opacity": [ + "HP:0007957" + ], + "corneal cloud": [ + "HP:0007957" + ], + "corneal clouding": [ + "HP:0007957" + ], + "corneal opacities": [ + "HP:0007957" + ], + "reduction of corneal clarity": [ + "HP:0007957" + ], + "scar or clouding of the cornea of the eye": [ + "HP:0007957" + ], + "scarring or clouding of the cornea of the eye": [ + "HP:0007957" + ], + "optic atrophy from cranial nerve compression": [ + "HP:0007958" + ], + "obsolete rarefaction of retinal pigmentation": [ + "HP:0007961" + ], + "speckle corneal dystrophy": [ + "HP:0007962" + ], + "speckled corneal dystrophy": [ + "HP:0007962" + ], + "pattern dystrophy of the retina": [ + "HP:0007963" + ], + "degenerative vitreoretinopathy": [ + "HP:0007964" + ], + "undetectable visual evoke potential": [ + "HP:0007965" + ], + "undetectable visual evoked potentials": [ + "HP:0007965" + ], + "absence of visual evoked potential": [ + "HP:0007965" + ], + "absence of visual evoked potentials": [ + "HP:0007965" + ], + "non - detectable vep": [ + "HP:0007965" + ], + "undetectable vep": [ + "HP:0007965" + ], + "remnant of the hyaloid vascular system": [ + "HP:0007968" + ], + "remnants of the hyaloid vascular system": [ + "HP:0007968" + ], + "congenital retinal septum": [ + "HP:0007968" + ], + "persistent fetal vasculature": [ + "HP:0007968" + ], + "persistent foetal vasculature": [ + "HP:0007968" + ], + "persistent hyperplasia of primary vitreous": [ + "HP:0007968" + ], + "persistent hyperplastic primary vitreous": [ + "HP:0007968" + ], + "persistent hypertrophic primary vitreous": [ + "HP:0007968" + ], + "persistent posterior fetal fibrovascular sheath of the lens": [ + "HP:0007968" + ], + "persistent posterior foetal fibrovascular sheath of the lens": [ + "HP:0007968" + ], + "persistent tunica vasculosa lentis": [ + "HP:0007968" + ], + "congenital ptosis": [ + "HP:0007970" + ], + "congenital droop upper eyelid": [ + "HP:0007970" + ], + "congenital drooping upper eyelid": [ + "HP:0007970" + ], + "lamellar cataract": [ + "HP:0007971" + ], + "retinal dysplasia": [ + "HP:0007973" + ], + "retinal dysgenesis": [ + "HP:0007973" + ], + "hypometric horizontal saccade": [ + "HP:0007975" + ], + "hypometric horizontal saccades": [ + "HP:0007975" + ], + "cerulean cataract": [ + "HP:0007976" + ], + "cataract , congenital , cerulean": [ + "HP:0007976" + ], + "cataracts , congenital , cerulean": [ + "HP:0007976" + ], + "gaze - evoked horizontal nystagmus": [ + "HP:0007979" + ], + "nystagmus , horizontal gaze - evoke": [ + "HP:0007979" + ], + "nystagmus , horizontal gaze - evoked": [ + "HP:0007979" + ], + "nystagmus , horizontal , gaze - evoke": [ + "HP:0007979" + ], + "nystagmus , horizontal , gaze - evoked": [ + "HP:0007979" + ], + "absent retinal pigment epithelium": [ + "HP:0007980" + ], + "obsolete concentric narrowing of visual field": [ + "HP:0007981" + ], + "obsolete central tapetoretinal dystrophy": [ + "HP:0007982" + ], + "electronegative electroretinogram": [ + "HP:0007984" + ], + "electronegative erg": [ + "HP:0007984" + ], + "electroretinogram : reduce b - wave amplitude": [ + "HP:0007984" + ], + "electroretinogram : reduced b - wave amplitude": [ + "HP:0007984" + ], + "reduce amplitude of dark - adapted bright flash electroretinogram b - wave": [ + "HP:0007984" + ], + "reduced amplitude of dark - adapted bright flash electroretinogram b - wave": [ + "HP:0007984" + ], + "reduce electroretinogram rod b - wave": [ + "HP:0007984" + ], + "reduced electroretinogram rod b - wave": [ + "HP:0007984" + ], + "reduce erg amplitude of b - wave": [ + "HP:0007984" + ], + "reduced erg amplitude of b - wave": [ + "HP:0007984" + ], + "retinal arteriolar occlusion": [ + "HP:0007985" + ], + "block retinal artery": [ + "HP:0007985" + ], + "blocked retinal artery": [ + "HP:0007985" + ], + "increase retinal vascularity": [ + "HP:0007986" + ], + "increased retinal vascularity": [ + "HP:0007986" + ], + "progressive visual field defect": [ + "HP:0007987" + ], + "progressive visual field defects": [ + "HP:0007987" + ], + "macular hypopigmentation": [ + "HP:0007988" + ], + "intraretinal exudate": [ + "HP:0007989" + ], + "hypoplastic iris stroma": [ + "HP:0007990" + ], + "hypoplastic iris stoma": [ + "HP:0007990" + ], + "iris stromal hypoplasia": [ + "HP:0007990" + ], + "underdeveloped iris stroma": [ + "HP:0007990" + ], + "lattice retinal degeneration": [ + "HP:0007992" + ], + "malformed lacrimal duct": [ + "HP:0007993" + ], + "malformed tear duct": [ + "HP:0007993" + ], + "malformed tear ducts": [ + "HP:0007993" + ], + "peripheral visual field loss": [ + "HP:0007994" + ], + "kalnienk vision": [ + "HP:0007994" + ], + "loss of peripheral vision": [ + "HP:0007994" + ], + "tunnel vision": [ + "HP:0007994" + ], + "decrease corneal reflex": [ + "HP:0008000" + ], + "decreased corneal reflex": [ + "HP:0008000" + ], + "decrease blink reflex": [ + "HP:0008000" + ], + "decreased blink reflex": [ + "HP:0008000" + ], + "reduce corneal reflex": [ + "HP:0008000" + ], + "reduced corneal reflex": [ + "HP:0008000" + ], + "foveal hyperpigmentation": [ + "HP:0008001" + ], + "abnormality of macular pigmentation": [ + "HP:0008002" + ], + "macular pigmentary change": [ + "HP:0008002" + ], + "macular pigmentary changes": [ + "HP:0008002" + ], + "jerky ocular pursuit movement": [ + "HP:0008003" + ], + "jerky ocular pursuit movements": [ + "HP:0008003" + ], + "jerky smooth pursuit": [ + "HP:0008003" + ], + "congenital corneal dystrophy": [ + "HP:0008005" + ], + "primary congenital glaucoma": [ + "HP:0008007" + ], + "obsolete progressive central visual loss": [ + "HP:0008008" + ], + "three row of eyelash": [ + "HP:0008009" + ], + "three rows of eyelashes": [ + "HP:0008009" + ], + "triple row of eyelash": [ + "HP:0008009" + ], + "triple row of eyelashes": [ + "HP:0008009" + ], + "peripheral opacification of the cornea": [ + "HP:0008011" + ], + "peripheral corneal opacity": [ + "HP:0008011" + ], + "obsolete congenital myopia": [ + "HP:0008012" + ], + "central fundal arteriolar microaneurysms": [ + "HP:0008014" + ], + "obsolete depigmented lesion of the retinal pigment epithelium": [ + "HP:0008017" + ], + "obsolete depigmented lesions of the retinal pigment epithelium": [ + "HP:0008017" + ], + "superior lens subluxation": [ + "HP:0008019" + ], + "superior subluxate lens": [ + "HP:0008019" + ], + "superior subluxated lens": [ + "HP:0008019" + ], + "cone dystrophy": [ + "HP:0008020" + ], + "progressive cone degeneration": [ + "HP:0008020" + ], + "progressive cone dystrophy": [ + "HP:0008020" + ], + "obsolete congenital nuclear cataract": [ + "HP:0008024" + ], + "horizontal opticokinetic nystagmus": [ + "HP:0008026" + ], + "cystoid macular degeneration": [ + "HP:0008028" + ], + "cystic macular degeneration": [ + "HP:0008028" + ], + "retinal arteritis": [ + "HP:0008030" + ], + "posterior y - sutural cataract": [ + "HP:0008031" + ], + "posterior y - sutural cataracts": [ + "HP:0008031" + ], + "obsolete congenital exotropia": [ + "HP:0008033" + ], + "abnormal iris pigmentation": [ + "HP:0008034" + ], + "retinitis pigmentosa inversa": [ + "HP:0008035" + ], + "central retinitis pigmentosa": [ + "HP:0008035" + ], + "obsolete rod - cone dystrophy": [ + "HP:0008036" + ], + "absent anterior chamber of the eye": [ + "HP:0008037" + ], + "aplastic / hypoplastic lacrimal gland": [ + "HP:0008038" + ], + "aplastic / hypoplastic lacrimal glands": [ + "HP:0008038" + ], + "absent / underdevelop lacrimal gland": [ + "HP:0008038" + ], + "absent / underdeveloped lacrimal glands": [ + "HP:0008038" + ], + "absent / underdevelop tear gland": [ + "HP:0008038" + ], + "absent / underdeveloped tear glands": [ + "HP:0008038" + ], + "subepithelial corneal opacity": [ + "HP:0008039" + ], + "subepithelial corneal opacities": [ + "HP:0008039" + ], + "late onset congenital glaucoma": [ + "HP:0008041" + ], + "retinal arteriolar constriction": [ + "HP:0008043" + ], + "constrict retinal arteriole": [ + "HP:0008043" + ], + "constricted retinal arterioles": [ + "HP:0008043" + ], + "narrow retinal arteriole": [ + "HP:0008043" + ], + "narrow retinal arterioles": [ + "HP:0008043" + ], + "retinal arteriolar narrowing": [ + "HP:0008043" + ], + "enlarge flash visual evoke potential": [ + "HP:0008045" + ], + "enlarged flash visual evoked potentials": [ + "HP:0008045" + ], + "high flash visual evoke potential": [ + "HP:0008045" + ], + "high flash visual evoked potentials": [ + "HP:0008045" + ], + "abnormal retinal vascular morphology": [ + "HP:0008046" + ], + "abnormality of retina blood vessel": [ + "HP:0008046" + ], + "abnormality of retina blood vessels": [ + "HP:0008046" + ], + "abnormality of the retinal vasculature": [ + "HP:0008046" + ], + "abnormality of the vasculature of the eye": [ + "HP:0008047" + ], + "abnormality of eye blood vessel": [ + "HP:0008047" + ], + "abnormality of eye blood vessels": [ + "HP:0008047" + ], + "abnormality of the line of schwalbe": [ + "HP:0008048" + ], + "abnormality of the extraocular muscle": [ + "HP:0008049" + ], + "abnormality of the extraocular muscles": [ + "HP:0008049" + ], + "abnormality of the palpebral fissure": [ + "HP:0008050" + ], + "abnormality of the palpebral fissures": [ + "HP:0008050" + ], + "abnormality of the opening between the eyelid": [ + "HP:0008050" + ], + "abnormality of the opening between the eyelids": [ + "HP:0008050" + ], + "deformity of the palpebral fissure": [ + "HP:0008050" + ], + "deformity of the palpebral fissures": [ + "HP:0008050" + ], + "malformation of the palpebral fissure": [ + "HP:0008050" + ], + "malformation of the palpebral fissures": [ + "HP:0008050" + ], + "obsolete abnormality of the retinal pigment epithelium": [ + "HP:0008051" + ], + "retinal fold": [ + "HP:0008052" + ], + "retinal folds": [ + "HP:0008052" + ], + "aplasia / hypoplasia of the iris": [ + "HP:0008053" + ], + "absent / small iris": [ + "HP:0008053" + ], + "absent / underdevelop iris": [ + "HP:0008053" + ], + "absent / underdeveloped iris": [ + "HP:0008053" + ], + "abnormal morphology of the conjunctival vasculature": [ + "HP:0008054" + ], + "abnormal morphology of the conjunctiva vasculature": [ + "HP:0008054" + ], + "abnormal vasculature of the conjunctiva morphology": [ + "HP:0008054" + ], + "abnormality of the vasculature of the conjunctiva": [ + "HP:0008054" + ], + "aplasia / hypoplasia affect the uvea": [ + "HP:0008055" + ], + "aplasia / hypoplasia affecting the uvea": [ + "HP:0008055" + ], + "absent / underdevelop uvea": [ + "HP:0008055" + ], + "absent / underdeveloped uvea": [ + "HP:0008055" + ], + "aplasia / hypoplasia affect the eye": [ + "HP:0008056" + ], + "aplasia / hypoplasia affecting the eye": [ + "HP:0008056" + ], + "absent / small eye": [ + "HP:0008056" + ], + "absent / underdevelop eye": [ + "HP:0008056" + ], + "absent / underdeveloped eye": [ + "HP:0008056" + ], + "aplasia / hypoplasia affect the fundus": [ + "HP:0008057" + ], + "aplasia / hypoplasia affecting the fundus": [ + "HP:0008057" + ], + "absent / small fundus": [ + "HP:0008057" + ], + "aplasia / hypoplasia of the optic nerve": [ + "HP:0008058" + ], + "absent / small optic nerve": [ + "HP:0008058" + ], + "absent / underdevelop optic nerve": [ + "HP:0008058" + ], + "absent / underdeveloped optic nerve": [ + "HP:0008058" + ], + "aplasia / hypoplasia of the macula": [ + "HP:0008059" + ], + "absent / underdevelop macula": [ + "HP:0008059" + ], + "absent / underdeveloped macula": [ + "HP:0008059" + ], + "aplasia / hypoplasia of the fovea": [ + "HP:0008060" + ], + "absent / underdevelop fovea": [ + "HP:0008060" + ], + "absent / underdeveloped fovea": [ + "HP:0008060" + ], + "aplasia / hypoplasia of the retina": [ + "HP:0008061" + ], + "absent / small retina": [ + "HP:0008061" + ], + "absent / underdevelop retina": [ + "HP:0008061" + ], + "absent / underdeveloped retina": [ + "HP:0008061" + ], + "aplasia / hypoplasia affect the anterior segment of the eye": [ + "HP:0008062" + ], + "aplasia / hypoplasia affecting the anterior segment of the eye": [ + "HP:0008062" + ], + "aplasia / hypoplasia of the lens": [ + "HP:0008063" + ], + "absent / small lens": [ + "HP:0008063" + ], + "absent / underdevelop lens": [ + "HP:0008063" + ], + "absent / underdeveloped lens": [ + "HP:0008063" + ], + "ichthyosis": [ + "HP:0008064" + ], + "hypertrophic ichthyosis": [ + "HP:0008064" + ], + "ichthyosiform abnormality of the skin": [ + "HP:0008064" + ], + "ichthyotic skin": [ + "HP:0008064" + ], + "aplasia / hypoplasia of the skin": [ + "HP:0008065" + ], + "absent / small skin": [ + "HP:0008065" + ], + "absent / underdevelop skin": [ + "HP:0008065" + ], + "absent / underdeveloped skin": [ + "HP:0008065" + ], + "abnormal blistering of the skin": [ + "HP:0008066" + ], + "blister": [ + "HP:0008066" + ], + "blistering , generalise": [ + "HP:0008066" + ], + "blistering , generalised": [ + "HP:0008066" + ], + "blistering , generalize": [ + "HP:0008066" + ], + "blistering , generalized": [ + "HP:0008066" + ], + "blisters": [ + "HP:0008066" + ], + "skin blister": [ + "HP:0008066" + ], + "skin blisters": [ + "HP:0008066" + ], + "skin bulla": [ + "HP:0008066" + ], + "skin bullae": [ + "HP:0008066" + ], + "abnormally lax or hyperextensible skin": [ + "HP:0008067" + ], + "abnormally loose or hyperelastic skin": [ + "HP:0008067" + ], + "abnormally loose or stretchable skin": [ + "HP:0008067" + ], + "neoplasm of the skin": [ + "HP:0008069" + ], + "dermatological tumor": [ + "HP:0008069" + ], + "dermatological tumors": [ + "HP:0008069" + ], + "dermatological tumour": [ + "HP:0008069" + ], + "dermatological tumours": [ + "HP:0008069" + ], + "neoplasia of the skin": [ + "HP:0008069" + ], + "skin cancer": [ + "HP:0008069" + ], + "skin cancer ( non - melanoma )": [ + "HP:0008069" + ], + "skin tumor": [ + "HP:0008069" + ], + "skin tumors": [ + "HP:0008069" + ], + "skin tumour": [ + "HP:0008069" + ], + "skin tumours": [ + "HP:0008069" + ], + "tumor of the skin": [ + "HP:0008069" + ], + "tumour of the skin": [ + "HP:0008069" + ], + "sparse hair": [ + "HP:0008070" + ], + "decrease hair growth": [ + "HP:0008070" + ], + "decreased hair growth": [ + "HP:0008070" + ], + "decrease hair growth on body": [ + "HP:0008070" + ], + "decreased hair growth on body": [ + "HP:0008070" + ], + "hypotrichosis": [ + "HP:0008070" + ], + "mark hypotrichosis": [ + "HP:0008070" + ], + "marked hypotrichosis": [ + "HP:0008070" + ], + "sparse hair since birth": [ + "HP:0008070" + ], + "thin , sparse hair": [ + "HP:0008070" + ], + "maternal hypertension": [ + "HP:0008071" + ], + "maternal virilization in pregnancy": [ + "HP:0008072" + ], + "low maternal serum estriol": [ + "HP:0008073" + ], + "metatarsal periosteal thicken": [ + "HP:0008074" + ], + "metatarsal periosteal thickening": [ + "HP:0008074" + ], + "progressive pe cavus": [ + "HP:0008075" + ], + "progressive pes cavus": [ + "HP:0008075" + ], + "osteoporotic tarsal": [ + "HP:0008076" + ], + "osteoporotic tarsals": [ + "HP:0008076" + ], + "thin metatarsal cortex": [ + "HP:0008078" + ], + "thin metatarsal cortices": [ + "HP:0008078" + ], + "absent fifth metatarsal": [ + "HP:0008079" + ], + "absent 5th long bone of foot": [ + "HP:0008079" + ], + "absent 5th metatarsal": [ + "HP:0008079" + ], + "absent 5th metatarsals": [ + "HP:0008079" + ], + "aplasia of the fifth metatarsal bone": [ + "HP:0008079" + ], + "hallux varus": [ + "HP:0008080" + ], + "medially deviate hallux": [ + "HP:0008080" + ], + "medially deviated halluces": [ + "HP:0008080" + ], + "pe valgus": [ + "HP:0008081" + ], + "pes valgus": [ + "HP:0008081" + ], + "valgus foot deformity": [ + "HP:0008081" + ], + "medial deviation of the foot": [ + "HP:0008082" + ], + "2nd - 5th toe middle phalangeal hypoplasia": [ + "HP:0008083" + ], + "underdeveloped 2nd - 5th middle toe bone": [ + "HP:0008083" + ], + "underdeveloped 2nd - 5th middle toe bones": [ + "HP:0008083" + ], + "nonossified fifth metatarsal": [ + "HP:0008087" + ], + "abnormality of the fifth metatarsal bone": [ + "HP:0008089" + ], + "abnormality of the 5th long bone of foot": [ + "HP:0008089" + ], + "ankylosis of foot small joint": [ + "HP:0008090" + ], + "ankylosis of feet small joints": [ + "HP:0008090" + ], + "short 4th toe": [ + "HP:0008093" + ], + "short fourth toe": [ + "HP:0008093" + ], + "widely space toe": [ + "HP:0008094" + ], + "widely spaced toes": [ + "HP:0008094" + ], + "osteolysis of talus": [ + "HP:0008095" + ], + "osteolysis of tali": [ + "HP:0008095" + ], + "medially deviate second toe": [ + "HP:0008096" + ], + "medially deviated second toe": [ + "HP:0008096" + ], + "partial fusion of tarsal": [ + "HP:0008097" + ], + "partial fusion of tarsals": [ + "HP:0008097" + ], + "expand metatarsal with widened medullary cavity": [ + "HP:0008102" + ], + "expanded metatarsals with widened medullary cavities": [ + "HP:0008102" + ], + "delay tarsal ossification": [ + "HP:0008103" + ], + "delayed tarsal ossification": [ + "HP:0008103" + ], + "delay ankle bone maturation": [ + "HP:0008103" + ], + "delayed ankle bone maturation": [ + "HP:0008103" + ], + "tarsal delay ossification": [ + "HP:0008103" + ], + "tarsal delayed ossification": [ + "HP:0008103" + ], + "plantar crease between first and second toe": [ + "HP:0008107" + ], + "plantar crease between first and second toes": [ + "HP:0008107" + ], + "advanced tarsal ossification": [ + "HP:0008108" + ], + "accelerate ankle bone maturation": [ + "HP:0008108" + ], + "accelerated ankle bone maturation": [ + "HP:0008108" + ], + "precociously ossify tarsal bone": [ + "HP:0008108" + ], + "precociously ossified tarsal bones": [ + "HP:0008108" + ], + "equinovarus deformity": [ + "HP:0008110" + ], + "broad distal hallux": [ + "HP:0008111" + ], + "broad distal big toe": [ + "HP:0008111" + ], + "plantar flexion contracture": [ + "HP:0008112" + ], + "plantar flexion contractures": [ + "HP:0008112" + ], + "multiple plantar crease": [ + "HP:0008113" + ], + "multiple plantar creases": [ + "HP:0008113" + ], + "metatarsal diaphyseal endosteal sclerosis": [ + "HP:0008114" + ], + "clinodactyly of the 3rd toe": [ + "HP:0008115" + ], + "3rd toe clinodactyly": [ + "HP:0008115" + ], + "curvature of 3rd toe": [ + "HP:0008115" + ], + "flexion limitation of toe": [ + "HP:0008116" + ], + "flexion limitation of toes": [ + "HP:0008116" + ], + "shortening of the talar neck": [ + "HP:0008117" + ], + "deform tarsal bone": [ + "HP:0008119" + ], + "deformed tarsal bones": [ + "HP:0008119" + ], + "deform ankle bone": [ + "HP:0008119" + ], + "deformed ankle bones": [ + "HP:0008119" + ], + "calcaneonavicular fusion": [ + "HP:0008122" + ], + "talipes calcaneovarus": [ + "HP:0008124" + ], + "second metatarsal posteriorly place": [ + "HP:0008125" + ], + "second metatarsal posteriorly placed": [ + "HP:0008125" + ], + "bipartite calcaneus": [ + "HP:0008127" + ], + "delay coalescence of bipartite calcaneus": [ + "HP:0008127" + ], + "delayed coalescence of bipartite calcanei": [ + "HP:0008127" + ], + "delay coalescence of calcaneal ossification center": [ + "HP:0008127" + ], + "delayed coalescence of calcaneal ossification centers": [ + "HP:0008127" + ], + "delay coalescence of calcaneal ossification centre": [ + "HP:0008127" + ], + "delayed coalescence of calcaneal ossification centres": [ + "HP:0008127" + ], + "delay fusion of bipartite calcaneus": [ + "HP:0008127" + ], + "delayed fusion of bipartite calcanei": [ + "HP:0008127" + ], + "double calcaneal ossification center": [ + "HP:0008127" + ], + "double calcaneal ossification centre": [ + "HP:0008127" + ], + "extra calcaneal ossification center": [ + "HP:0008127" + ], + "extra calcaneal ossification centre": [ + "HP:0008127" + ], + "tarsal stipple": [ + "HP:0008131" + ], + "tarsal stippling": [ + "HP:0008131" + ], + "punctate calcification of tarsal": [ + "HP:0008131" + ], + "punctate calcifications of tarsals": [ + "HP:0008131" + ], + "punctate tarsal calcification": [ + "HP:0008131" + ], + "medial rotation of the medial malleolus": [ + "HP:0008132" + ], + "distal tapering of metatarsal": [ + "HP:0008133" + ], + "distal tapering of metatarsals": [ + "HP:0008133" + ], + "irregular tarsal ossification": [ + "HP:0008134" + ], + "irregular ankle bone maturation": [ + "HP:0008134" + ], + "irregular tarsal center": [ + "HP:0008134" + ], + "irregular tarsal centers": [ + "HP:0008134" + ], + "irregular tarsal centre": [ + "HP:0008134" + ], + "irregular tarsal centres": [ + "HP:0008134" + ], + "equinus calcaneus": [ + "HP:0008138" + ], + "equinus deformity of the calcaneus": [ + "HP:0008138" + ], + "hindfoot equinus": [ + "HP:0008138" + ], + "dislocation of toe": [ + "HP:0008141" + ], + "dislocation of toes": [ + "HP:0008141" + ], + "delay calcaneal ossification": [ + "HP:0008142" + ], + "delayed calcaneal ossification": [ + "HP:0008142" + ], + "delay heel bone maturation": [ + "HP:0008142" + ], + "delayed heel bone maturation": [ + "HP:0008142" + ], + "flattening of the talar dome": [ + "HP:0008144" + ], + "impaired epinephrine - induced platelet aggregation": [ + "HP:0008148" + ], + "elevate serum transaminase during infection": [ + "HP:0008150" + ], + "elevated serum transaminases during infections": [ + "HP:0008150" + ], + "prolong prothrombin time": [ + "HP:0008151" + ], + "prolonged prothrombin time": [ + "HP:0008151" + ], + "increase inr": [ + "HP:0008151" + ], + "increased inr": [ + "HP:0008151" + ], + "increase international normalised ratio": [ + "HP:0008151" + ], + "increased international normalised ratio": [ + "HP:0008151" + ], + "increase international normalized ratio": [ + "HP:0008151" + ], + "increased international normalized ratio": [ + "HP:0008151" + ], + "low factor ii activity": [ + "HP:0008151" + ], + "prolong pt": [ + "HP:0008151" + ], + "prolonged pt": [ + "HP:0008151" + ], + "reduce factor ii activity": [ + "HP:0008151" + ], + "reduced factor ii activity": [ + "HP:0008151" + ], + "reduce prothrombin activity": [ + "HP:0008151" + ], + "reduced prothrombin activity": [ + "HP:0008151" + ], + "periodic hypokalemic paresis": [ + "HP:0008153" + ], + "hypokalemic periodic paresis": [ + "HP:0008153" + ], + "mucopolysacchariduria": [ + "HP:0008155" + ], + "hyperapobetalipoproteinemia": [ + "HP:0008158" + ], + "3 - hydroxydicarboxylic aciduria": [ + "HP:0008160" + ], + "absent leukocyte alkaline phosphatase": [ + "HP:0008161" + ], + "absent leukocyte alp": [ + "HP:0008161" + ], + "asymptomatic hyperammonemia": [ + "HP:0008162" + ], + "hyperammonemia , asymptomatic": [ + "HP:0008162" + ], + "decrease circulate cortisol level": [ + "HP:0008163" + ], + "decreased circulating cortisol level": [ + "HP:0008163" + ], + "decrease cortisol production": [ + "HP:0008163" + ], + "decreased cortisol production": [ + "HP:0008163" + ], + "glucocorticoid insufficiency": [ + "HP:0008163" + ], + "hypocortisolemia": [ + "HP:0008163" + ], + "hypocortisolism": [ + "HP:0008163" + ], + "low blood cortisol level": [ + "HP:0008163" + ], + "low to undetectable plasma cortisol": [ + "HP:0008163" + ], + "plasma cortisol low": [ + "HP:0008163" + ], + "decrease helper t cell proportion": [ + "HP:0008165" + ], + "decreased helper t cell proportion": [ + "HP:0008165" + ], + "decrease proportion circulate t - helper cell": [ + "HP:0008165" + ], + "decreased proportion circulating t - helper cells": [ + "HP:0008165" + ], + "reduce helper t cell proportion": [ + "HP:0008165" + ], + "reduced helper t cell proportion": [ + "HP:0008165" + ], + "decrease beta - galactosidase activity": [ + "HP:0008166" + ], + "decreased beta - galactosidase activity": [ + "HP:0008166" + ], + "beta - galactosidase deficiency in fibroblast and white blood cell": [ + "HP:0008166" + ], + "beta - galactosidase deficiency in fibroblasts and white blood cells": [ + "HP:0008166" + ], + "beta - galactosidase - 1 deficiency": [ + "HP:0008166" + ], + "decrease beta galactosidase activity": [ + "HP:0008166" + ], + "decreased beta galactosidase activity": [ + "HP:0008166" + ], + "very long chain fatty acid accumulation": [ + "HP:0008167" + ], + "reduce factor vii activity": [ + "HP:0008169" + ], + "reduced factor vii activity": [ + "HP:0008169" + ], + "factor vii deficiency": [ + "HP:0008169" + ], + "neonatal unconjugated hyperbilirubinemia": [ + "HP:0008176" + ], + "abnormal cartilage matrix": [ + "HP:0008178" + ], + "decrease arden ratio of electrooculogram": [ + "HP:0008179" + ], + "decreased arden ratio of electrooculogram": [ + "HP:0008179" + ], + "decrease arden ratio of eog": [ + "HP:0008179" + ], + "decreased arden ratio of eog": [ + "HP:0008179" + ], + "mildly elevated creatine kinase": [ + "HP:0008180" + ], + "mildly elevate cpk": [ + "HP:0008180" + ], + "mildly elevated cpk": [ + "HP:0008180" + ], + "mildly elevated creatine phosphokinase": [ + "HP:0008180" + ], + "mildly elevate serum ck": [ + "HP:0008180" + ], + "mildly elevated serum ck": [ + "HP:0008180" + ], + "mildly elevate serum cpk": [ + "HP:0008180" + ], + "mildly elevated serum cpk": [ + "HP:0008180" + ], + "mildly elevate serum phospho - ck": [ + "HP:0008180" + ], + "mildly elevated serum phospho - ck": [ + "HP:0008180" + ], + "mildly increased creatine kinase": [ + "HP:0008180" + ], + "mildly increase serum creatine kinase": [ + "HP:0008180" + ], + "mildly increased serum creatine kinase": [ + "HP:0008180" + ], + "moderately elevate serum ck": [ + "HP:0008180" + ], + "moderately elevated serum ck": [ + "HP:0008180" + ], + "moderately elevate serum cpk": [ + "HP:0008180" + ], + "moderately elevated serum cpk": [ + "HP:0008180" + ], + "moderately increased serum creatine kinase": [ + "HP:0008180" + ], + "abetalipoproteinemia": [ + "HP:0008181" + ], + "adrenocortical hypoplasia": [ + "HP:0008182" + ], + "small adrenal cortex": [ + "HP:0008182" + ], + "precocious puberty in male": [ + "HP:0008185" + ], + "precocious puberty in males": [ + "HP:0008185" + ], + "early onset of puberty in male": [ + "HP:0008185" + ], + "early onset of puberty in males": [ + "HP:0008185" + ], + "male precocious puberty": [ + "HP:0008185" + ], + "adrenocortical cytomegaly": [ + "HP:0008186" + ], + "absence of secondary sex characteristic": [ + "HP:0008187" + ], + "absence of secondary sex characteristics": [ + "HP:0008187" + ], + "no secondary sexual characteristic at puberty": [ + "HP:0008187" + ], + "no secondary sexual characteristics at puberty": [ + "HP:0008187" + ], + "thyroid dysgenesis": [ + "HP:0008188" + ], + "thyroid dysplasia": [ + "HP:0008188" + ], + "insulin insensitivity": [ + "HP:0008189" + ], + "thyroid agenesis": [ + "HP:0008191" + ], + "athyroidal hypothyroidism": [ + "HP:0008191" + ], + "primary gonadal insufficiency": [ + "HP:0008193" + ], + "multiple pancreatic beta - cell adenoma": [ + "HP:0008194" + ], + "multiple pancreatic beta - cell adenomas": [ + "HP:0008194" + ], + "absence of pubertal development": [ + "HP:0008197" + ], + "congenital hypoparathyroidism": [ + "HP:0008198" + ], + "neonatal hypoparathyroidism": [ + "HP:0008198" + ], + "primary hyperparathyroidism": [ + "HP:0008200" + ], + "reduce circulate prolactin concentration": [ + "HP:0008202" + ], + "reduced circulating prolactin concentration": [ + "HP:0008202" + ], + "prolactin deficiency": [ + "HP:0008202" + ], + "precocious puberty with sertoli cell tumor": [ + "HP:0008204" + ], + "precocious puberty with sertoli cell tumour": [ + "HP:0008204" + ], + "insulin - dependent but ketosis - resistant diabetes": [ + "HP:0008205" + ], + "primary adrenal insufficiency": [ + "HP:0008207" + ], + "addison disease": [ + "HP:0008207" + ], + "addison 's disease": [ + "HP:0008207" + ], + "adrenocortical insufficiency": [ + "HP:0008207" + ], + "primary adrenocortical failure": [ + "HP:0008207" + ], + "parathyroid hyperplasia": [ + "HP:0008208" + ], + "enlarge parathyroid gland": [ + "HP:0008208" + ], + "enlarged parathyroid glands": [ + "HP:0008208" + ], + "premature ovarian insufficiency": [ + "HP:0008209" + ], + "climacterium praecox": [ + "HP:0008209" + ], + "early menopause": [ + "HP:0008209" + ], + "hypergonadotropic amenorrhea": [ + "HP:0008209" + ], + "menopause praecox": [ + "HP:0008209" + ], + "premature menopause": [ + "HP:0008209" + ], + "premature ovarian failure": [ + "HP:0008209" + ], + "primary ovarian insufficiency": [ + "HP:0008209" + ], + "parathyroid agenesis": [ + "HP:0008211" + ], + "parathyroid absence": [ + "HP:0008211" + ], + "parathyroid aplasia": [ + "HP:0008211" + ], + "gonadotropin deficiency": [ + "HP:0008213" + ], + "pituitary gonadotropin deficiency": [ + "HP:0008213" + ], + "decrease serum estradiol": [ + "HP:0008214" + ], + "decreased serum estradiol": [ + "HP:0008214" + ], + "adrenal gland dysgenesis": [ + "HP:0008216" + ], + "adrenal gland dysplasia": [ + "HP:0008216" + ], + "dysplastic adrenal gland": [ + "HP:0008216" + ], + "dysplastic adrenal glands": [ + "HP:0008216" + ], + "adrenal hyperplasia": [ + "HP:0008221" + ], + "enlarge adrenal gland": [ + "HP:0008221" + ], + "enlarged adrenal glands": [ + "HP:0008221" + ], + "female infertility": [ + "HP:0008222" + ], + "compensate hypothyroidism": [ + "HP:0008223" + ], + "compensated hypothyroidism": [ + "HP:0008223" + ], + "mild hypothyroidism": [ + "HP:0008223" + ], + "subclinical hypothyroidism": [ + "HP:0008223" + ], + "thyroid follicular hyperplasia": [ + "HP:0008225" + ], + "androgen insufficiency": [ + "HP:0008226" + ], + "hypoandrogenism": [ + "HP:0008226" + ], + "pituitary resistance to thyroid hormone": [ + "HP:0008227" + ], + "thyroid lymphangiectasia": [ + "HP:0008229" + ], + "thyroid lymphangiectasis": [ + "HP:0008229" + ], + "obsolete decrease testosterone in male": [ + "HP:0008230" + ], + "obsolete decreased testosterone in males": [ + "HP:0008230" + ], + "macronodular adrenal hyperplasia": [ + "HP:0008231" + ], + "elevate circulate follicle stimulate hormone level": [ + "HP:0008232" + ], + "elevated circulating follicle stimulating hormone level": [ + "HP:0008232" + ], + "elevate follicle stimulate hormone": [ + "HP:0008232" + ], + "elevated follicle stimulating hormone": [ + "HP:0008232" + ], + "elevate follicle - stimulating hormone": [ + "HP:0008232" + ], + "elevated follicle - stimulating hormone": [ + "HP:0008232" + ], + "elevate fsh level": [ + "HP:0008232" + ], + "elevated fsh level": [ + "HP:0008232" + ], + "elevate plasma follicle stimulate hormone": [ + "HP:0008232" + ], + "elevated plasma follicle stimulating hormone": [ + "HP:0008232" + ], + "increase circulate follicle stimulate hormone level": [ + "HP:0008232" + ], + "increased circulating follicle stimulating hormone level": [ + "HP:0008232" + ], + "decrease circulate progesterone": [ + "HP:0008233" + ], + "decreased circulating progesterone": [ + "HP:0008233" + ], + "decrease serum progesterone": [ + "HP:0008233" + ], + "decreased serum progesterone": [ + "HP:0008233" + ], + "isosexual precocious puberty": [ + "HP:0008236" + ], + "hypothalamic hypothyroidism": [ + "HP:0008237" + ], + "tertiary hypothyroidism": [ + "HP:0008237" + ], + "adrenal medullary hypoplasia": [ + "HP:0008239" + ], + "small adrenal medulla": [ + "HP:0008239" + ], + "secondary growth hormone deficiency": [ + "HP:0008240" + ], + "pseudohypoaldosteronism": [ + "HP:0008242" + ], + "congenital adrenal hypoplasia": [ + "HP:0008244" + ], + "congenital adrenal gland hypoplasia": [ + "HP:0008244" + ], + "pituitary hypothyroidism": [ + "HP:0008245" + ], + "low thyroid gland function due to abnormal pituitary gland": [ + "HP:0008245" + ], + "secondary hypothyroidism": [ + "HP:0008245" + ], + "thyroid stimulate hormone deficiency": [ + "HP:0008245" + ], + "thyroid stimulating hormone deficiency": [ + "HP:0008245" + ], + "thyrotropin deficiency": [ + "HP:0008245" + ], + "tsh deficient hypothyroidism": [ + "HP:0008245" + ], + "euthyroid hyperthyroxinemia": [ + "HP:0008247" + ], + "asymptomatic hyperthyroxinemia": [ + "HP:0008247" + ], + "thyroid hyperplasia": [ + "HP:0008249" + ], + "large thyroid": [ + "HP:0008249" + ], + "infantile hypercalcemia": [ + "HP:0008250" + ], + "congenital goiter": [ + "HP:0008251" + ], + "congenital goitre": [ + "HP:0008251" + ], + "transient neonatal diabetes mellitus": [ + "HP:0008255" + ], + "adrenocortical adenoma": [ + "HP:0008256" + ], + "adrenocortical adenomas": [ + "HP:0008256" + ], + "congenital adrenal hyperplasia": [ + "HP:0008258" + ], + "adrenocorticotropin receptor defect": [ + "HP:0008259" + ], + "acth receptor defect": [ + "HP:0008259" + ], + "acthr defect": [ + "HP:0008259" + ], + "adrenocorticotropic hormone - resistant adrenal insufficiency": [ + "HP:0008259" + ], + "pancreatic islet cell adenoma": [ + "HP:0008261" + ], + "thyroid defect in oxidation and organification of iodide": [ + "HP:0008263" + ], + "neutrophil inclusion body": [ + "HP:0008264" + ], + "neutrophil inclusion bodies": [ + "HP:0008264" + ], + "mitochondrial lysine transport defect": [ + "HP:0008265" + ], + "increase red cell hemolysis by shear stress": [ + "HP:0008269" + ], + "increased red cell hemolysis by shear stress": [ + "HP:0008269" + ], + "abnormal cartilage collagen": [ + "HP:0008271" + ], + "abnormal hyaline collagen": [ + "HP:0008271" + ], + "abnormal type ii collagen": [ + "HP:0008271" + ], + "renal tubular lysine transport defect": [ + "HP:0008272" + ], + "transient aminoaciduria": [ + "HP:0008273" + ], + "abnormal light - adapt electroretinogram": [ + "HP:0008275" + ], + "abnormal light - adapted electroretinogram": [ + "HP:0008275" + ], + "abnormal cone - mediate electroretinogram": [ + "HP:0008275" + ], + "abnormal cone - mediated electroretinogram": [ + "HP:0008275" + ], + "abnormal blood zinc concentration": [ + "HP:0008277" + ], + "abnormal zinc metabolism": [ + "HP:0008277" + ], + "abnormality of zinc homeostasis": [ + "HP:0008277" + ], + "cerebellar cortical atrophy": [ + "HP:0008278" + ], + "cerebellar cortex degeneration": [ + "HP:0008278" + ], + "transient hyperlipidemia": [ + "HP:0008279" + ], + "acute hyperammonemia": [ + "HP:0008281" + ], + "hyperammonemia , acute": [ + "HP:0008281" + ], + "unconjugated hyperbilirubinemia": [ + "HP:0008282" + ], + "fast hyperinsulinemia": [ + "HP:0008283" + ], + "fasting hyperinsulinemia": [ + "HP:0008283" + ], + "high blood insulin level while fast": [ + "HP:0008283" + ], + "high blood insulin levels while fasting": [ + "HP:0008283" + ], + "transient hypophosphatemia": [ + "HP:0008285" + ], + "nonketotic hyperglycinemia": [ + "HP:0008288" + ], + "partial complement factor h deficiency": [ + "HP:0008290" + ], + "pituitary corticotropic cell adenoma": [ + "HP:0008291" + ], + "acth - produce pituitary adenoma": [ + "HP:0008291" + ], + "acth - producing pituitary adenoma": [ + "HP:0008291" + ], + "corticotropin - secrete pituitary adenoma": [ + "HP:0008291" + ], + "corticotropin - secreting pituitary adenoma": [ + "HP:0008291" + ], + "long - chain dicarboxylic aciduria": [ + "HP:0008293" + ], + "transient hyperphenylalaninemia": [ + "HP:0008297" + ], + "dermatan sulfate excretion in urine": [ + "HP:0008301" + ], + "dermatan sulphate excretion in urine": [ + "HP:0008301" + ], + "olivary degeneration": [ + "HP:0008303" + ], + "exercise - induced myoglobinuria": [ + "HP:0008305" + ], + "exercise - induced myoglobinuria in adult": [ + "HP:0008305" + ], + "exercise - induced myoglobinuria in adults": [ + "HP:0008305" + ], + "abnormal iron deposition in mitochondrion": [ + "HP:0008306" + ], + "abnormal iron deposition in mitochondria": [ + "HP:0008306" + ], + "medium chain dicarboxylic aciduria": [ + "HP:0008309" + ], + "spinal cord posterior column myelin loss": [ + "HP:0008311" + ], + "spinal cord posterior columns myelin loss": [ + "HP:0008311" + ], + "decreased activity of mitochondrial complex ii": [ + "HP:0008314" + ], + "respiratory complex ii deficiency": [ + "HP:0008314" + ], + "decrease plasma free carnitine": [ + "HP:0008315" + ], + "decreased plasma free carnitine": [ + "HP:0008315" + ], + "abnormal mitochondrion in muscle tissue": [ + "HP:0008316" + ], + "abnormal mitochondria in muscle tissue": [ + "HP:0008316" + ], + "abnormal mitochondrion in muscle": [ + "HP:0008316" + ], + "abnormal mitochondria in muscle": [ + "HP:0008316" + ], + "elevate leukocyte alkaline phosphatase": [ + "HP:0008318" + ], + "elevated leukocyte alkaline phosphatase": [ + "HP:0008318" + ], + "elevate leukocyte alp": [ + "HP:0008318" + ], + "elevated leukocyte alp": [ + "HP:0008318" + ], + "impaired collagen - induced platelet aggregation": [ + "HP:0008320" + ], + "reduce factor x activity": [ + "HP:0008321" + ], + "reduced factor x activity": [ + "HP:0008321" + ], + "decrease factor x activity": [ + "HP:0008321" + ], + "decreased factor x activity": [ + "HP:0008321" + ], + "factor x deficiency": [ + "HP:0008321" + ], + "abnormal mitochondrial morphology": [ + "HP:0008322" + ], + "abnormal mitochondrion morphology": [ + "HP:0008322" + ], + "abnormal light - and dark - adapt electroretinogram": [ + "HP:0008323" + ], + "abnormal light - and dark - adapted electroretinogram": [ + "HP:0008323" + ], + "abnormal rod and cone electroretinogram": [ + "HP:0008323" + ], + "reduce circulate vitamin b6 level": [ + "HP:0008326" + ], + "reduced circulating vitamin b6 level": [ + "HP:0008326" + ], + "reduce vitamin b6 level": [ + "HP:0008326" + ], + "reduced vitamin b6 levels": [ + "HP:0008326" + ], + "vitamin b6 deficiency": [ + "HP:0008326" + ], + "microscopic nephrocalcinosis": [ + "HP:0008327" + ], + "reduce von willebrand factor activity": [ + "HP:0008330" + ], + "reduced von willebrand factor activity": [ + "HP:0008330" + ], + "decrease von willebrand factor activity": [ + "HP:0008330" + ], + "decreased von willebrand factor activity": [ + "HP:0008330" + ], + "elevate creatine kinase after exercise": [ + "HP:0008331" + ], + "elevated creatine kinase after exercise": [ + "HP:0008331" + ], + "elevate ck after exercise": [ + "HP:0008331" + ], + "elevated ck after exercise": [ + "HP:0008331" + ], + "elevate cpk after exercise": [ + "HP:0008331" + ], + "elevated cpk after exercise": [ + "HP:0008331" + ], + "elevate creatine phosphokinase after exercise": [ + "HP:0008331" + ], + "elevated creatine phosphokinase after exercise": [ + "HP:0008331" + ], + "elevate phospho - ck after exercise": [ + "HP:0008331" + ], + "elevated phospho - ck after exercise": [ + "HP:0008331" + ], + "elevate phospho - creatine kinase after exercise": [ + "HP:0008331" + ], + "elevated phospho - creatine kinase after exercise": [ + "HP:0008331" + ], + "increase ck after exercise": [ + "HP:0008331" + ], + "increased ck after exercise": [ + "HP:0008331" + ], + "increase creatine kinase after exercise": [ + "HP:0008331" + ], + "increased creatine kinase after exercise": [ + "HP:0008331" + ], + "increase creatine phosphokinase after exercise": [ + "HP:0008331" + ], + "increased creatine phosphokinase after exercise": [ + "HP:0008331" + ], + "increase phospho - ck after exercise": [ + "HP:0008331" + ], + "increased phospho - ck after exercise": [ + "HP:0008331" + ], + "increase phospho - creatine kinase after exercise": [ + "HP:0008331" + ], + "increased phospho - creatine kinase after exercise": [ + "HP:0008331" + ], + "obsolete renal aminoaciduria": [ + "HP:0008335" + ], + "complex organic aciduria": [ + "HP:0008336" + ], + "partial functional complement factor d deficiency": [ + "HP:0008338" + ], + "partial functional adipsin deficiency": [ + "HP:0008338" + ], + "partial functional factor d deficiency": [ + "HP:0008338" + ], + "diaminoaciduria": [ + "HP:0008339" + ], + "distal renal tubular acidosis": [ + "HP:0008341" + ], + "renal tubular acidosis , type i": [ + "HP:0008341" + ], + "elevate plasma branch chain amino acid": [ + "HP:0008344" + ], + "elevated plasma branched chain amino acids": [ + "HP:0008344" + ], + "hypoplasia of the iris dilator muscle": [ + "HP:0008345" + ], + "hypoplasia of the pupil dilator muscle": [ + "HP:0008345" + ], + "underdeveloped iris dilator muscle": [ + "HP:0008345" + ], + "underdeveloped pupil dilator muscle": [ + "HP:0008345" + ], + "increase red cell sickling tendency": [ + "HP:0008346" + ], + "increased red cell sickling tendency": [ + "HP:0008346" + ], + "increase sickling of erythrocyte": [ + "HP:0008346" + ], + "increased sickling of erythrocytes": [ + "HP:0008346" + ], + "increase sickling of red cell": [ + "HP:0008346" + ], + "increased sickling of red cells": [ + "HP:0008346" + ], + "decreased activity of mitochondrial complex iv": [ + "HP:0008347" + ], + "respiratory complex iv deficiency": [ + "HP:0008347" + ], + "decrease circulate igg2 level": [ + "HP:0008348" + ], + "decreased circulating igg2 level": [ + "HP:0008348" + ], + "decrease igg2 level in blood": [ + "HP:0008348" + ], + "decreased igg2 level in blood": [ + "HP:0008348" + ], + "immunoglobulin igg2 deficiency": [ + "HP:0008348" + ], + "reduce igg2 level": [ + "HP:0008348" + ], + "reduced igg2 levels": [ + "HP:0008348" + ], + "impaired platelet adhesion": [ + "HP:0008352" + ], + "impaired thrombocyte adhesion": [ + "HP:0008352" + ], + "impaired thrombocytes adhesion": [ + "HP:0008352" + ], + "neutral hyperaminoaciduria": [ + "HP:0008353" + ], + "factor x activation deficiency": [ + "HP:0008354" + ], + "obsolete combine hyperlipidemia": [ + "HP:0008356" + ], + "obsolete combined hyperlipidemia": [ + "HP:0008356" + ], + "reduce factor xiii activity": [ + "HP:0008357" + ], + "reduced factor xiii activity": [ + "HP:0008357" + ], + "hyperprolinemia": [ + "HP:0008358" + ], + "prolinemia": [ + "HP:0008358" + ], + "neonatal hypoproteinemia": [ + "HP:0008360" + ], + "corticospinal tract pallor": [ + "HP:0008361" + ], + "aplasia / hypoplasia of the hallux": [ + "HP:0008362" + ], + "absent / small big toe": [ + "HP:0008362" + ], + "absent / underdevelop big toe": [ + "HP:0008362" + ], + "absent / underdeveloped big toe": [ + "HP:0008362" + ], + "aplastic / hypoplastic hallux": [ + "HP:0008362" + ], + "aplastic / hypoplastic halluces": [ + "HP:0008362" + ], + "aplasia / hypoplasia of the tarsal bone": [ + "HP:0008363" + ], + "aplasia / hypoplasia of the tarsal bones": [ + "HP:0008363" + ], + "absent / small ankle bone": [ + "HP:0008363" + ], + "absent / underdevelop ankle bone": [ + "HP:0008363" + ], + "absent / underdeveloped ankle bone": [ + "HP:0008363" + ], + "aplastic / hypoplastic tarsal": [ + "HP:0008363" + ], + "aplastic / hypoplastic tarsals": [ + "HP:0008363" + ], + "abnormality of the calcaneus": [ + "HP:0008364" + ], + "abnormal heel bone": [ + "HP:0008364" + ], + "abnormal talus morphology": [ + "HP:0008365" + ], + "abnormal large bone of ankle": [ + "HP:0008365" + ], + "contracture involve the joint of the foot": [ + "HP:0008366" + ], + "contractures involving the joints of the feet": [ + "HP:0008366" + ], + "contracture of the foot joint": [ + "HP:0008366" + ], + "contractures of the foot joints": [ + "HP:0008366" + ], + "tarsal synostosis": [ + "HP:0008368" + ], + "fuse ankle bone": [ + "HP:0008368" + ], + "fused ankle bones": [ + "HP:0008368" + ], + "synostosis involve tarsal bone": [ + "HP:0008368" + ], + "synostosis involving tarsal bones": [ + "HP:0008368" + ], + "synostosis of tarsal bone": [ + "HP:0008368" + ], + "synostosis of tarsal bones": [ + "HP:0008368" + ], + "tarsal bone fusion": [ + "HP:0008368" + ], + "tarsal bone synostosis": [ + "HP:0008368" + ], + "tarsal fusion": [ + "HP:0008368" + ], + "tarsal fusions": [ + "HP:0008368" + ], + "abnormal tarsal ossification": [ + "HP:0008369" + ], + "abnormal maturation of ankle bone": [ + "HP:0008369" + ], + "abnormal maturation of ankle bones": [ + "HP:0008369" + ], + "abnormal ossification of tarsal bone": [ + "HP:0008369" + ], + "abnormal ossification of tarsal bones": [ + "HP:0008369" + ], + "hardening of ankle bone": [ + "HP:0008369" + ], + "hardening of ankle bones": [ + "HP:0008369" + ], + "abnormal metatarsal ossification": [ + "HP:0008371" + ], + "abnormal maturation of long bone of foot": [ + "HP:0008371" + ], + "abnormal ossification involve metatarsal bone": [ + "HP:0008371" + ], + "abnormal ossification involving metatarsal bones": [ + "HP:0008371" + ], + "abnormality of vitamin a metabolism": [ + "HP:0008372" + ], + "puberty and gonadal disorder": [ + "HP:0008373" + ], + "puberty and gonadal disorders": [ + "HP:0008373" + ], + "nasal , dysarthic speech": [ + "HP:0008376" + ], + "breathy speech": [ + "HP:0008376" + ], + "slow - grow nail": [ + "HP:0008383" + ], + "slow - growing nails": [ + "HP:0008383" + ], + "aplasia / hypoplasia of the nail": [ + "HP:0008386" + ], + "aplasia / hypoplasia of the nails": [ + "HP:0008386" + ], + "absent / hypoplastic nail": [ + "HP:0008386" + ], + "absent / hypoplastic nails": [ + "HP:0008386" + ], + "absent / small nail": [ + "HP:0008386" + ], + "absent / small nails": [ + "HP:0008386" + ], + "absent / underdevelop nail": [ + "HP:0008386" + ], + "absent / underdeveloped nails": [ + "HP:0008386" + ], + "nail aplasia / hypoplasia": [ + "HP:0008386" + ], + "abnormal toenail morphology": [ + "HP:0008388" + ], + "abnormality of the toenail": [ + "HP:0008388" + ], + "abnormality of the toenails": [ + "HP:0008388" + ], + "recurrent loss of toenail and fingernail": [ + "HP:0008390" + ], + "recurrent loss of toenails and fingernails": [ + "HP:0008390" + ], + "recurrent shed of toenail and fingernail": [ + "HP:0008390" + ], + "recurrent shedding of toenails and fingernails": [ + "HP:0008390" + ], + "dystrophic fingernail": [ + "HP:0008391" + ], + "dystrophic fingernails": [ + "HP:0008391" + ], + "poor fingernail formation": [ + "HP:0008391" + ], + "subungual hyperkeratosis": [ + "HP:0008392" + ], + "thicken , discolor skin under nail": [ + "HP:0008392" + ], + "thickened , discolored skin under nail": [ + "HP:0008392" + ], + "thicken , discolour skin under nail": [ + "HP:0008392" + ], + "thickened , discoloured skin under nail": [ + "HP:0008392" + ], + "congenital curve nail of fourth toe": [ + "HP:0008393" + ], + "congenital curved nail of fourth toe": [ + "HP:0008393" + ], + "congenital onychodystrophy": [ + "HP:0008394" + ], + "congenital malformed nail": [ + "HP:0008394" + ], + "congenital malformed nails": [ + "HP:0008394" + ], + "chronic monilial nail infection": [ + "HP:0008396" + ], + "hypoplastic fifth fingernail": [ + "HP:0008398" + ], + "underdeveloped fifth fingernail": [ + "HP:0008398" + ], + "underdeveloped fingernail of little finger": [ + "HP:0008398" + ], + "underdeveloped fingernail of pinkie finger": [ + "HP:0008398" + ], + "underdeveloped fingernail of pinky finger": [ + "HP:0008398" + ], + "circumungual hyperkeratosis": [ + "HP:0008399" + ], + "thick skin around nail": [ + "HP:0008399" + ], + "thick skin around nails": [ + "HP:0008399" + ], + "onycholysis of distal fingernail": [ + "HP:0008400" + ], + "onycholysis of distal fingernails": [ + "HP:0008400" + ], + "detachment of outermost fingernail": [ + "HP:0008400" + ], + "detachment of outermost fingernails": [ + "HP:0008400" + ], + "onychogryposis of toenail": [ + "HP:0008401" + ], + "onychogryposis of toenails": [ + "HP:0008401" + ], + "overgrowth and curving of toenail": [ + "HP:0008401" + ], + "overgrowth and curving of toenails": [ + "HP:0008401" + ], + "ridge fingernail": [ + "HP:0008402" + ], + "ridged fingernail": [ + "HP:0008402" + ], + "longitudinally groove fingernail": [ + "HP:0008402" + ], + "longitudinally grooved fingernails": [ + "HP:0008402" + ], + "ridged fingernails": [ + "HP:0008402" + ], + "nail dystrophy": [ + "HP:0008404" + ], + "dystrophic nail": [ + "HP:0008404" + ], + "dystrophic nails": [ + "HP:0008404" + ], + "onychodystrophy": [ + "HP:0008404" + ], + "poor nail formation": [ + "HP:0008404" + ], + "hyperconvex thumb nail": [ + "HP:0008407" + ], + "hyperconvex thumb nails": [ + "HP:0008407" + ], + "tightly curve thumb nail": [ + "HP:0008407" + ], + "tightly curved thumb nail": [ + "HP:0008407" + ], + "subungual hyperkeratotic fragment": [ + "HP:0008410" + ], + "subungual hyperkeratotic fragments": [ + "HP:0008410" + ], + "lumbar kyphosis in infancy": [ + "HP:0008414" + ], + "hunch back in infancy": [ + "HP:0008414" + ], + "hunched back in infancy": [ + "HP:0008414" + ], + "round back in infancy": [ + "HP:0008414" + ], + "six lumbar vertebra": [ + "HP:0008416" + ], + "six lumbar vertebrae": [ + "HP:0008416" + ], + "vertebral hypoplasia": [ + "HP:0008417" + ], + "underdeveloped vertebra": [ + "HP:0008417" + ], + "underdeveloped vertebrae": [ + "HP:0008417" + ], + "square - off platyspondyly": [ + "HP:0008418" + ], + "squared - off platyspondyly": [ + "HP:0008418" + ], + "intervertebral disc degeneration": [ + "HP:0008419" + ], + "degeneration of intervertebral disc": [ + "HP:0008419" + ], + "degeneration of intervertebral discs": [ + "HP:0008419" + ], + "degeneration of intervertebral disk": [ + "HP:0008419" + ], + "degeneration of intervertebral disks": [ + "HP:0008419" + ], + "degenerative disc disease": [ + "HP:0008419" + ], + "degenerative intervertebral disc": [ + "HP:0008419" + ], + "degenerative intervertebral disk": [ + "HP:0008419" + ], + "punctate vertebral calcification": [ + "HP:0008420" + ], + "punctate vertebral calcifications": [ + "HP:0008420" + ], + "tall lumbar vertebral body": [ + "HP:0008421" + ], + "tall lumbar vertebral bodies": [ + "HP:0008421" + ], + "vertebral wedging": [ + "HP:0008422" + ], + "anterior wedge": [ + "HP:0008422" + ], + "anterior wedging": [ + "HP:0008422" + ], + "wedge - shape vertebra": [ + "HP:0008422" + ], + "wedge - shaped vertebrae": [ + "HP:0008422" + ], + "wedge vertebra": [ + "HP:0008422" + ], + "wedged vertebrae": [ + "HP:0008422" + ], + "spinal dysplasia": [ + "HP:0008423" + ], + "hypoplastic 5th lumbar vertebra": [ + "HP:0008424" + ], + "hypoplastic 5th lumbar vertebrae": [ + "HP:0008424" + ], + "underdeveloped 5th lumbar vertebra": [ + "HP:0008424" + ], + "underdeveloped 5th lumbar vertebrae": [ + "HP:0008424" + ], + "cuboid - shaped thoracolumbar vertebral body": [ + "HP:0008425" + ], + "cuboid - shaped thoracolumbar vertebral bodies": [ + "HP:0008425" + ], + "vertebral clefting": [ + "HP:0008428" + ], + "vertebral cleft": [ + "HP:0008428" + ], + "vertebral clefts": [ + "HP:0008428" + ], + "anterior beaking of lumbar vertebra": [ + "HP:0008430" + ], + "anterior beaking of lumbar vertebrae": [ + "HP:0008430" + ], + "anterior tongue - like protrusion of lumbar vertebral body": [ + "HP:0008430" + ], + "anterior tongue - like protrusion of lumbar vertebral bodies": [ + "HP:0008430" + ], + "anterior wedging of l1": [ + "HP:0008432" + ], + "reverse usual vertebral column curve": [ + "HP:0008433" + ], + "reversed usual vertebral column curves": [ + "HP:0008433" + ], + "hypoplastic cervical vertebra": [ + "HP:0008434" + ], + "hypoplastic cervical vertebrae": [ + "HP:0008434" + ], + "cervical vertebra hypoplasia": [ + "HP:0008434" + ], + "cervical vertebrae hypoplasia": [ + "HP:0008434" + ], + "underdeveloped cervical vertebra": [ + "HP:0008434" + ], + "underdeveloped cervical vertebrae": [ + "HP:0008434" + ], + "absent in utero ossification of vertebral body": [ + "HP:0008435" + ], + "absent in utero ossification of vertebral bodies": [ + "HP:0008435" + ], + "absent / hypoplastic coccyx": [ + "HP:0008436" + ], + "absent / small tailbone": [ + "HP:0008436" + ], + "absent / underdevelop tailbone": [ + "HP:0008436" + ], + "absent / underdeveloped tailbone": [ + "HP:0008436" + ], + "bifid thoracic vertebra": [ + "HP:0008437" + ], + "bifid thoracic vertebrae": [ + "HP:0008437" + ], + "vertebral arch anomaly": [ + "HP:0008438" + ], + "vertebral arch abnormality": [ + "HP:0008438" + ], + "vertebral arch abnormalities": [ + "HP:0008438" + ], + "lumbar hemivertebrae": [ + "HP:0008439" + ], + "c1 - c2 vertebral abnormality": [ + "HP:0008440" + ], + "herniation of intervertebral nucleus": [ + "HP:0008441" + ], + "herniation of intervertebral nuclei": [ + "HP:0008441" + ], + "herniated disc": [ + "HP:0008441" + ], + "herniated disk": [ + "HP:0008441" + ], + "herniated intervertebral nucleus": [ + "HP:0008441" + ], + "herniated intervertebral nuclei": [ + "HP:0008441" + ], + "vertebral hyperostosis": [ + "HP:0008442" + ], + "spinal deformity": [ + "HP:0008443" + ], + "spinal deformities": [ + "HP:0008443" + ], + "posterior wedging of vertebral body": [ + "HP:0008444" + ], + "posterior wedging of vertebral bodies": [ + "HP:0008444" + ], + "posterior wedging": [ + "HP:0008444" + ], + "cervical spinal canal stenosis": [ + "HP:0008445" + ], + "narrow cervical spinal canal": [ + "HP:0008445" + ], + "hypoplastic coccygeal vertebra": [ + "HP:0008447" + ], + "hypoplastic coccygeal vertebrae": [ + "HP:0008447" + ], + "progressive cervical vertebral spine fusion": [ + "HP:0008449" + ], + "narrow vertebral interpedicular distance": [ + "HP:0008450" + ], + "interpedicular narrowing": [ + "HP:0008450" + ], + "narrow interpedicular space": [ + "HP:0008450" + ], + "narrow interpediculate distance": [ + "HP:0008450" + ], + "narrow interpediculate distances": [ + "HP:0008450" + ], + "narrowing of interpediculate distance": [ + "HP:0008450" + ], + "narrowing of interpediculate distances": [ + "HP:0008450" + ], + "posterior vertebral hypoplasia": [ + "HP:0008451" + ], + "wafer - thin platyspondyly": [ + "HP:0008452" + ], + "congenital kyphoscoliosis": [ + "HP:0008453" + ], + "lumbar kyphosis": [ + "HP:0008454" + ], + "lumbar gibbus deformity": [ + "HP:0008454" + ], + "round low back": [ + "HP:0008454" + ], + "rounded lower back": [ + "HP:0008454" + ], + "dysplastic sacrum": [ + "HP:0008455" + ], + "absence of some of the sacral and coccygeal bone": [ + "HP:0008455" + ], + "absence of some of the sacral and coccygeal bones": [ + "HP:0008455" + ], + "partial sacral agenesis": [ + "HP:0008455" + ], + "sacral dysgenesis": [ + "HP:0008455" + ], + "c2 - c3 subluxation": [ + "HP:0008456" + ], + "caudal interpedicular narrowing": [ + "HP:0008457" + ], + "caudal narrowing of interpedicular distance": [ + "HP:0008457" + ], + "caudal narrowing of interpedicular distances": [ + "HP:0008457" + ], + "progressive congenital scoliosis": [ + "HP:0008458" + ], + "cervical vertebral agenesis": [ + "HP:0008459" + ], + "cervical vertebra agenesis": [ + "HP:0008459" + ], + "cervical vertebrae agenesis": [ + "HP:0008459" + ], + "miss cervical vertebra": [ + "HP:0008459" + ], + "missing cervical vertebrae": [ + "HP:0008459" + ], + "hypoplastic spinal process": [ + "HP:0008460" + ], + "hypoplastic spinal processes": [ + "HP:0008460" + ], + "underdeveloped spinal process": [ + "HP:0008460" + ], + "underdeveloped spinal processes": [ + "HP:0008460" + ], + "cervical vertebral facet hypoplasia": [ + "HP:0008461" + ], + "cervical instability": [ + "HP:0008462" + ], + "central vertebral hypoplasia": [ + "HP:0008463" + ], + "absent spinous process of low thoracic and lumbar vertebra": [ + "HP:0008464" + ], + "absent spinous processes of lower thoracic and lumbar vertebrae": [ + "HP:0008464" + ], + "absent vertebra": [ + "HP:0008465" + ], + "absent vertebrae": [ + "HP:0008465" + ], + "thoracic hemivertebrae": [ + "HP:0008467" + ], + "midthoracic hemivertebrae": [ + "HP:0008467" + ], + "abnormal sacral segmentation": [ + "HP:0008468" + ], + "cervical vertebral dysplasia": [ + "HP:0008469" + ], + "low thoracic interpediculate narrowness": [ + "HP:0008470" + ], + "lower thoracic interpediculate narrowness": [ + "HP:0008470" + ], + "narrowness of interpediculate distance in low thoracic region": [ + "HP:0008470" + ], + "narrowness of interpediculate distances in lower thoracic regions": [ + "HP:0008470" + ], + "prominent protruding coccyx": [ + "HP:0008472" + ], + "large tailbone": [ + "HP:0008472" + ], + "prominent protrude tailbone": [ + "HP:0008472" + ], + "prominent protruding tailbone": [ + "HP:0008472" + ], + "narrow anterio - posterior vertebral body diameter": [ + "HP:0008473" + ], + "reduce anterior - posterior diameter of vertebral body": [ + "HP:0008473" + ], + "reduced anterior - posterior diameter of vertebral bodies": [ + "HP:0008473" + ], + "reduce sagittal diameter of vertebra": [ + "HP:0008473" + ], + "reduced sagittal diameter of vertebrae": [ + "HP:0008473" + ], + "hypoplastic sacral vertebra": [ + "HP:0008475" + ], + "hypoplastic sacral vertebrae": [ + "HP:0008475" + ], + "irregular sclerotic endplate": [ + "HP:0008476" + ], + "irregular sclerotic endplates": [ + "HP:0008476" + ], + "irregular , dense end plate": [ + "HP:0008476" + ], + "poorly ossify cervical vertebra": [ + "HP:0008477" + ], + "poorly ossified cervical vertebrae": [ + "HP:0008477" + ], + "scheuermann - like vertebral change": [ + "HP:0008478" + ], + "scheuermann - like vertebral changes": [ + "HP:0008478" + ], + "hypoplastic vertebral body": [ + "HP:0008479" + ], + "hypoplastic vertebral bodies": [ + "HP:0008479" + ], + "small vertebra": [ + "HP:0008479" + ], + "small vertebrae": [ + "HP:0008479" + ], + "small vertebral body": [ + "HP:0008479" + ], + "small vertebral bodies": [ + "HP:0008479" + ], + "underdeveloped back bone": [ + "HP:0008479" + ], + "underdeveloped back bones": [ + "HP:0008479" + ], + "cervical spondylosis": [ + "HP:0008480" + ], + "cervical oestoarthritis": [ + "HP:0008480" + ], + "neck arthritis": [ + "HP:0008480" + ], + "asymmetry of spinal facet joint": [ + "HP:0008482" + ], + "asymmetry of spinal facet joints": [ + "HP:0008482" + ], + "cervical vertebral body with decreased anteroposterior diameter": [ + "HP:0008483" + ], + "cervical vertebral bodies with decreased anteroposterior diameter": [ + "HP:0008483" + ], + "thoracolumbar interpediculate narrowness": [ + "HP:0008484" + ], + "narrow thoracolumbar interpediculate distance": [ + "HP:0008484" + ], + "lumbar interpedicular narrowing": [ + "HP:0008486" + ], + "decrease lumbar vertebra interpediculate distance": [ + "HP:0008486" + ], + "decreasing lumbar vertebrae interpediculate distance": [ + "HP:0008486" + ], + "anterior rounding of vertebral body": [ + "HP:0008488" + ], + "anterior rounding of vertebral bodies": [ + "HP:0008488" + ], + "spondylolisthesis at l5 - s1": [ + "HP:0008489" + ], + "spondylolysis and spondylolisthesis of l5": [ + "HP:0008489" + ], + "sacral segmentation defect": [ + "HP:0008490" + ], + "premature anterior fontanel closure": [ + "HP:0008491" + ], + "inferior lens subluxation": [ + "HP:0008494" + ], + "inferior subluxate lens": [ + "HP:0008494" + ], + "inferior subluxated lens": [ + "HP:0008494" + ], + "multiple row of eyelash": [ + "HP:0008496" + ], + "multiple rows of eyelashes": [ + "HP:0008496" + ], + "double row of eyelash": [ + "HP:0008496" + ], + "double row of eyelashes": [ + "HP:0008496" + ], + "extra row of eyelash": [ + "HP:0008496" + ], + "extra rows of eyelashes": [ + "HP:0008496" + ], + "two row of eyelash": [ + "HP:0008496" + ], + "two rows of eyelashes": [ + "HP:0008496" + ], + "congenital craniofacial dysostosis": [ + "HP:0008497" + ], + "no permanent dentition": [ + "HP:0008498" + ], + "absence of adult teeth": [ + "HP:0008498" + ], + "absence of secondary dentition": [ + "HP:0008498" + ], + "miss adult teeth": [ + "HP:0008498" + ], + "missing adult teeth": [ + "HP:0008498" + ], + "no adult dentition": [ + "HP:0008498" + ], + "no secondary dentition": [ + "HP:0008498" + ], + "high hypermetropia": [ + "HP:0008499" + ], + "high hyperopia": [ + "HP:0008499" + ], + "high - grade hypermetropia": [ + "HP:0008499" + ], + "severe farsightedness": [ + "HP:0008499" + ], + "severe long - sightedness": [ + "HP:0008499" + ], + "median cleft lip and palate": [ + "HP:0008501" + ], + "central cleft lip and palate": [ + "HP:0008501" + ], + "medial cleft lip and palate": [ + "HP:0008501" + ], + "midline cleft lip / palate": [ + "HP:0008501" + ], + "wide midline cleft lip / palate": [ + "HP:0008501" + ], + "moderate sensorineural hearing impairment": [ + "HP:0008504" + ], + "moderate neural deafness": [ + "HP:0008504" + ], + "static ophthalmoparesis": [ + "HP:0008507" + ], + "age leonine appearance": [ + "HP:0008509" + ], + "aged leonine appearance": [ + "HP:0008509" + ], + "central posterior corneal opacity": [ + "HP:0008511" + ], + "bilateral conductive hearing impairment": [ + "HP:0008513" + ], + "bilateral conductive deafness": [ + "HP:0008513" + ], + "bilateral conductive hearing loss": [ + "HP:0008513" + ], + "aplasia / hypoplasia of the vertebra": [ + "HP:0008515" + ], + "aplasia / hypoplasia of the vertebrae": [ + "HP:0008515" + ], + "absent / small vertebra": [ + "HP:0008515" + ], + "absent / small vertebrae": [ + "HP:0008515" + ], + "absent / underdevelop vertebra": [ + "HP:0008515" + ], + "absent / underdeveloped vertebrae": [ + "HP:0008515" + ], + "abnormality of the vertebral spinous process": [ + "HP:0008516" + ], + "abnormality of the vertebral spinous processes": [ + "HP:0008516" + ], + "aplasia / hypoplasia of the sacrum": [ + "HP:0008517" + ], + "absent / small sacrum": [ + "HP:0008517" + ], + "absent / underdevelop sacrum": [ + "HP:0008517" + ], + "absent / underdeveloped sacrum": [ + "HP:0008517" + ], + "aplasia / hypoplasia involve the vertebral column": [ + "HP:0008518" + ], + "aplasia / hypoplasia involving the vertebral column": [ + "HP:0008518" + ], + "absent / small backbone": [ + "HP:0008518" + ], + "absent / small spine": [ + "HP:0008518" + ], + "absent / small vertebral column": [ + "HP:0008518" + ], + "absent / underdevelop backbone": [ + "HP:0008518" + ], + "absent / underdeveloped backbone": [ + "HP:0008518" + ], + "absent / underdevelop spine": [ + "HP:0008518" + ], + "absent / underdeveloped spine": [ + "HP:0008518" + ], + "absent / underdevelop vertebral column": [ + "HP:0008518" + ], + "absent / underdeveloped vertebral column": [ + "HP:0008518" + ], + "abnormal coccyx morphology": [ + "HP:0008519" + ], + "abnormal tailbone": [ + "HP:0008519" + ], + "abnormality of the coccyx": [ + "HP:0008519" + ], + "posterior helix pit": [ + "HP:0008523" + ], + "ear , posterior helical groove": [ + "HP:0008523" + ], + "ear , posterior helical notch": [ + "HP:0008523" + ], + "helix , posterior pit": [ + "HP:0008523" + ], + "indentation in back of outer ear": [ + "HP:0008523" + ], + "pit in posterior aspect of ear helix": [ + "HP:0008523" + ], + "pits in posterior aspect of ear helices": [ + "HP:0008523" + ], + "congenital sensorineural hearing impairment": [ + "HP:0008527" + ], + "bilateral congenital sensorineural deafness": [ + "HP:0008527" + ], + "congenital neurosensory deafness": [ + "HP:0008527" + ], + "congenital perceptive deafness": [ + "HP:0008527" + ], + "congenital sensorineural deafness": [ + "HP:0008527" + ], + "congenital sensorineural hearing loss": [ + "HP:0008527" + ], + "hearing loss , congenital sensorineural": [ + "HP:0008527" + ], + "long hair grow from helix of pinna": [ + "HP:0008528" + ], + "long hairs growing from helix of pinna": [ + "HP:0008528" + ], + "ear hair": [ + "HP:0008528" + ], + "long hair grow from helix of ear": [ + "HP:0008528" + ], + "long hairs growing from helix of ear": [ + "HP:0008528" + ], + "absence of acoustic reflex": [ + "HP:0008529" + ], + "absence of acoustic middle ear muscle reflex": [ + "HP:0008529" + ], + "absence of acoustic middle ear muscle reflexes": [ + "HP:0008529" + ], + "absent middle ear reflex": [ + "HP:0008529" + ], + "absent middle ear reflexes": [ + "HP:0008529" + ], + "cleft at the superior portion of the pinna": [ + "HP:0008537" + ], + "cleft at the superior portion of the ear": [ + "HP:0008537" + ], + "superiorly displace ear": [ + "HP:0008541" + ], + "superiorly displaced ears": [ + "HP:0008541" + ], + "high set ear": [ + "HP:0008541" + ], + "high set ears": [ + "HP:0008541" + ], + "low - frequency hearing loss": [ + "HP:0008542" + ], + "abnormally fold helix": [ + "HP:0008544" + ], + "abnormally folded helix": [ + "HP:0008544" + ], + "microtia": [ + "HP:0008551" + ], + "bilateral microtia": [ + "HP:0008551" + ], + "hypoplasia of the external ear": [ + "HP:0008551" + ], + "hypoplastic ear": [ + "HP:0008551" + ], + "hypoplastic ears": [ + "HP:0008551" + ], + "hypoplastic pinna": [ + "HP:0008551" + ], + "small ear": [ + "HP:0008551" + ], + "small ears": [ + "HP:0008551" + ], + "small pinna": [ + "HP:0008551" + ], + "small pinnae": [ + "HP:0008551" + ], + "underdeveloped ear": [ + "HP:0008551" + ], + "underdeveloped ears": [ + "HP:0008551" + ], + "cochlear malformation": [ + "HP:0008554" + ], + "absent vestibular function": [ + "HP:0008555" + ], + "hypoplastic superior helix": [ + "HP:0008559" + ], + "underdeveloped superior helix": [ + "HP:0008559" + ], + "underdeveloped superior helices": [ + "HP:0008559" + ], + "vestibular areflexia": [ + "HP:0008568" + ], + "vestibular ataxia": [ + "HP:0008568" + ], + "microtia , second degree": [ + "HP:0008569" + ], + "cockleshell ear": [ + "HP:0008569" + ], + "constrict helix type iv": [ + "HP:0008569" + ], + "constricted helix type iv": [ + "HP:0008569" + ], + "ear , grade ii dysplasia": [ + "HP:0008569" + ], + "mini ear": [ + "HP:0008569" + ], + "severe cup ear , type iii": [ + "HP:0008569" + ], + "severe cupped ear , type iii": [ + "HP:0008569" + ], + "shell ear": [ + "HP:0008569" + ], + "snail ear": [ + "HP:0008569" + ], + "low - frequency sensorineural hearing impairment": [ + "HP:0008573" + ], + "low - frequency sensorineural hearing loss": [ + "HP:0008573" + ], + "underfolded helix": [ + "HP:0008577" + ], + "poorly fold helix": [ + "HP:0008577" + ], + "poorly folded helices": [ + "HP:0008577" + ], + "underfolded superior helix": [ + "HP:0008583" + ], + "underfolded superior helices": [ + "HP:0008583" + ], + "hypoplasia of the cochlea": [ + "HP:0008586" + ], + "hypoplastic cochlea": [ + "HP:0008586" + ], + "underdeveloped cochlea": [ + "HP:0008586" + ], + "mild neurosensory hearing impairment": [ + "HP:0008587" + ], + "mild neurosensory hearing loss": [ + "HP:0008587" + ], + "slit - like opening of the exterior auditory meatus": [ + "HP:0008588" + ], + "hypoplastic helix": [ + "HP:0008589" + ], + "hypoplastic helices": [ + "HP:0008589" + ], + "underdeveloped helix": [ + "HP:0008589" + ], + "underdeveloped helices": [ + "HP:0008589" + ], + "congenital conductive hearing impairment": [ + "HP:0008591" + ], + "congenital conductive deafness": [ + "HP:0008591" + ], + "congenital conductive hearing loss": [ + "HP:0008591" + ], + "prominent antitragus": [ + "HP:0008593" + ], + "enlarge antitragus": [ + "HP:0008593" + ], + "enlarged antitragus": [ + "HP:0008593" + ], + "hyperplastic antitragus": [ + "HP:0008593" + ], + "hypertrophic antitragus": [ + "HP:0008593" + ], + "postlingual sensorineural hearing impairment": [ + "HP:0008596" + ], + "mild conductive hearing impairment": [ + "HP:0008598" + ], + "conductive hearing loss , mild": [ + "HP:0008598" + ], + "unilateral external ear deformity": [ + "HP:0008605" + ], + "deform external ear on one side": [ + "HP:0008605" + ], + "deformed external ear on one side": [ + "HP:0008605" + ], + "supraauricular pit": [ + "HP:0008606" + ], + "pit above the ear": [ + "HP:0008606" + ], + "supraauricular fistula": [ + "HP:0008606" + ], + "supraauricular sinus": [ + "HP:0008606" + ], + "supraauricular sinuses": [ + "HP:0008606" + ], + "progressive conductive hearing impairment": [ + "HP:0008607" + ], + "progressive conductive deafness": [ + "HP:0008607" + ], + "hypertrophic auricular cartilage": [ + "HP:0008608" + ], + "morphological abnormality of the middle ear": [ + "HP:0008609" + ], + "middle ear malformation": [ + "HP:0008609" + ], + "infantile sensorineural hearing impairment": [ + "HP:0008610" + ], + "infantile sensorineural hearing loss": [ + "HP:0008610" + ], + "adult onset sensorineural hearing impairment": [ + "HP:0008615" + ], + "late sensorineural hearing loss": [ + "HP:0008615" + ], + "sensorineural deafness , late - onset": [ + "HP:0008615" + ], + "bilateral sensorineural hearing impairment": [ + "HP:0008619" + ], + "bilateral nerve deafness": [ + "HP:0008619" + ], + "bilateral sensorineural deafness": [ + "HP:0008619" + ], + "bilateral sensorineural hearing loss": [ + "HP:0008619" + ], + "hearing loss , sensorineural , bilateral": [ + "HP:0008619" + ], + "severe sensorineural hearing impairment": [ + "HP:0008625" + ], + "severe sensorineural deafness": [ + "HP:0008625" + ], + "severe sensorineural hearing loss": [ + "HP:0008625" + ], + "abnormality of the stapes": [ + "HP:0008628" + ], + "stapedial abnormality": [ + "HP:0008628" + ], + "stapedial abnormalities": [ + "HP:0008628" + ], + "pulsatile tinnitus": [ + "HP:0008629" + ], + "ureteral dysgenesis": [ + "HP:0008631" + ], + "agonadism": [ + "HP:0008633" + ], + "absent gonadal tissue": [ + "HP:0008633" + ], + "gonadal agenesis": [ + "HP:0008633" + ], + "hypertrophy of the urinary bladder": [ + "HP:0008635" + ], + "hypertrophic urinary bladder": [ + "HP:0008635" + ], + "lobular glomerulopathy": [ + "HP:0008636" + ], + "gonadal hypoplasia": [ + "HP:0008639" + ], + "underdeveloped gonad": [ + "HP:0008639" + ], + "congenital macroorchidism": [ + "HP:0008640" + ], + "nephroblastomatosis": [ + "HP:0008643" + ], + "pubertal developmental failure in female": [ + "HP:0008647" + ], + "pubertal developmental failure in females": [ + "HP:0008647" + ], + "anteriorly displace urethral meatus": [ + "HP:0008648" + ], + "anteriorly displaced urethral meatus": [ + "HP:0008648" + ], + "uric acid urolithiasis independent of gout": [ + "HP:0008651" + ], + "autonomic erectile dysfunction": [ + "HP:0008652" + ], + "impotence due to autonomic dysfunction": [ + "HP:0008652" + ], + "crescentic glomerulonephritis": [ + "HP:0008653" + ], + "aplasia / hypoplasia of the fallopian tube": [ + "HP:0008655" + ], + "absent or rudimentary fallopian tube": [ + "HP:0008655" + ], + "absent or rudimentary fallopian tubes": [ + "HP:0008655" + ], + "absent / small fallopian tube": [ + "HP:0008655" + ], + "absent / underdevelop fallopian tube": [ + "HP:0008655" + ], + "absent / underdeveloped fallopian tube": [ + "HP:0008655" + ], + "incomplete male pseudohermaphroditism": [ + "HP:0008656" + ], + "multiple small medullary renal cyst": [ + "HP:0008659" + ], + "multiple small medullary renal cysts": [ + "HP:0008659" + ], + "medullary cystic disease": [ + "HP:0008659" + ], + "medullary sponge kidney disease": [ + "HP:0008659" + ], + "renotubular dysgenesis": [ + "HP:0008660" + ], + "renal tubular dysgenesis": [ + "HP:0008660" + ], + "urethral stenosis": [ + "HP:0008661" + ], + "narrowing of the urethra": [ + "HP:0008661" + ], + "renal sarcoma": [ + "HP:0008663" + ], + "urethral sphincter sclerosis": [ + "HP:0008664" + ], + "clitoral hypertrophy": [ + "HP:0008665" + ], + "clitoral enlargement": [ + "HP:0008665" + ], + "clitoromegaly": [ + "HP:0008665" + ], + "enlarge clitoris": [ + "HP:0008665" + ], + "enlarged clitoris": [ + "HP:0008665" + ], + "hypertrophic clitoris": [ + "HP:0008665" + ], + "prominent clitoris": [ + "HP:0008665" + ], + "impaired histidine renal tubular absorption": [ + "HP:0008666" + ], + "gonadal dysgenesis , male": [ + "HP:0008668" + ], + "46 , xy gonadal dysgenesis": [ + "HP:0008668" + ], + "abnormal spermatogenesis": [ + "HP:0008669" + ], + "abnormal sperm development": [ + "HP:0008669" + ], + "impaired spermatogenesis": [ + "HP:0008669" + ], + "partial vaginal septum": [ + "HP:0008670" + ], + "calcium oxalate nephrolithiasis": [ + "HP:0008672" + ], + "ca oxalate kidney stone": [ + "HP:0008672" + ], + "ca oxalate nephrolithiasis": [ + "HP:0008672" + ], + "ca oxalate urolithiasis": [ + "HP:0008672" + ], + "ca2+ oxalate kidney stone": [ + "HP:0008672" + ], + "ca2+ oxalate nephrolithiasis": [ + "HP:0008672" + ], + "ca2+ oxalate urolithiasis": [ + "HP:0008672" + ], + "calcium oxalate kidney stone": [ + "HP:0008672" + ], + "calcium oxalate kidney stones": [ + "HP:0008672" + ], + "calcium oxalate urolithiasis": [ + "HP:0008672" + ], + "oxalate nephrolithiasis": [ + "HP:0008672" + ], + "enlarge polycystic ovary": [ + "HP:0008675" + ], + "enlarged polycystic ovaries": [ + "HP:0008675" + ], + "enlarged ovary with cyst": [ + "HP:0008675" + ], + "enlarged ovaries with cysts": [ + "HP:0008675" + ], + "congenital megaureter": [ + "HP:0008676" + ], + "congenital megaloureter": [ + "HP:0008676" + ], + "congenital nephrotic syndrome": [ + "HP:0008677" + ], + "congenital nephrosis": [ + "HP:0008677" + ], + "renal hypoplasia / aplasia": [ + "HP:0008678" + ], + "absent / small kidney": [ + "HP:0008678" + ], + "absent / underdevelop kidney": [ + "HP:0008678" + ], + "absent / underdeveloped kidney": [ + "HP:0008678" + ], + "renal agenesis / hypoplasia": [ + "HP:0008678" + ], + "renal aplasia / hypoplasia": [ + "HP:0008678" + ], + "renal tubular epithelial necrosis": [ + "HP:0008682" + ], + "acute tubular necrosis": [ + "HP:0008682" + ], + "renal tubular necrosis": [ + "HP:0008682" + ], + "enlarge labium minora": [ + "HP:0008683" + ], + "enlarged labia minora": [ + "HP:0008683" + ], + "hypertrophic labium minora": [ + "HP:0008683" + ], + "hypertrophic labia minora": [ + "HP:0008683" + ], + "labia minora hypertrophy": [ + "HP:0008683" + ], + "aplasia / hypoplasia of the uterus": [ + "HP:0008684" + ], + "absent / small uterus": [ + "HP:0008684" + ], + "absent / underdevelop uterus": [ + "HP:0008684" + ], + "absent / underdeveloped uterus": [ + "HP:0008684" + ], + "hypoplasia of the prostate": [ + "HP:0008687" + ], + "hypoplastic prostate": [ + "HP:0008687" + ], + "underdeveloped prostate": [ + "HP:0008687" + ], + "bilateral cryptorchidism": [ + "HP:0008689" + ], + "cryptorchidism , bilateral": [ + "HP:0008689" + ], + "solitary bladder diverticulum": [ + "HP:0008691" + ], + "obsolete hypertrophic labium minora": [ + "HP:0008694" + ], + "obsolete hypertrophic labia minora": [ + "HP:0008694" + ], + "transient nephrotic syndrome": [ + "HP:0008695" + ], + "transient nephrosis": [ + "HP:0008695" + ], + "renal hamartoma": [ + "HP:0008696" + ], + "hypoplasia of the fallopian tube": [ + "HP:0008697" + ], + "rudimentary fallopian tube": [ + "HP:0008697" + ], + "rudimentary fallopian tubes": [ + "HP:0008697" + ], + "underdeveloped fallopian tube": [ + "HP:0008697" + ], + "absent internal genitalia": [ + "HP:0008702" + ], + "gonadal calcification": [ + "HP:0008703" + ], + "ureteral triplication": [ + "HP:0008705" + ], + "distal urethral duplication": [ + "HP:0008706" + ], + "absent scrotum": [ + "HP:0008707" + ], + "partial development of the penile shaft": [ + "HP:0008708" + ], + "benign prostatic hyperplasia": [ + "HP:0008711" + ], + "benign prostatic hypertrophy": [ + "HP:0008711" + ], + "ureterovesical stenosis": [ + "HP:0008714" + ], + "testicular dysgenesis": [ + "HP:0008715" + ], + "urethrovaginal fistula": [ + "HP:0008716" + ], + "urethrovaginal fistulae": [ + "HP:0008716" + ], + "unilateral renal atrophy": [ + "HP:0008717" + ], + "kidney degeneration on one side": [ + "HP:0008717" + ], + "unilateral kidney wasting": [ + "HP:0008717" + ], + "unilateral renal dysplasia": [ + "HP:0008718" + ], + "primary testicular failure": [ + "HP:0008720" + ], + "urethral diverticulum": [ + "HP:0008722" + ], + "gonadal dysgenesis with female appearance , male": [ + "HP:0008723" + ], + "xy female gonadal dysgenesis": [ + "HP:0008723" + ], + "hypoplasia of the ovary": [ + "HP:0008724" + ], + "hypoplastic ovary": [ + "HP:0008724" + ], + "underdeveloped ovary": [ + "HP:0008724" + ], + "hypoplasia of the vagina": [ + "HP:0008726" + ], + "hypoplastic vagina": [ + "HP:0008726" + ], + "rudimentary vagina": [ + "HP:0008726" + ], + "underdeveloped vagina": [ + "HP:0008726" + ], + "absence of labium majora": [ + "HP:0008729" + ], + "absence of labia majora": [ + "HP:0008729" + ], + "absent vaginal lip": [ + "HP:0008729" + ], + "absent vaginal lips": [ + "HP:0008729" + ], + "female external genitalia in individual with 46 , xy karyotype": [ + "HP:0008730" + ], + "male with female external genitalia": [ + "HP:0008730" + ], + "males with female external genitalia": [ + "HP:0008730" + ], + "renal hypophosphatemia": [ + "HP:0008732" + ], + "dysplastic testis": [ + "HP:0008733" + ], + "dysplastic testes": [ + "HP:0008733" + ], + "decrease testicular size": [ + "HP:0008734" + ], + "decreased testicular size": [ + "HP:0008734" + ], + "hypoplastic testis": [ + "HP:0008734" + ], + "hypoplastic testes": [ + "HP:0008734" + ], + "small testis": [ + "HP:0008734" + ], + "small testes": [ + "HP:0008734" + ], + "testicular hypoplasia": [ + "HP:0008734" + ], + "hypoplasia of penis": [ + "HP:0008736" + ], + "underdeveloped penis": [ + "HP:0008736" + ], + "partially duplicate kidney": [ + "HP:0008738" + ], + "partially duplicated kidney": [ + "HP:0008738" + ], + "labial pseudohypertrophy": [ + "HP:0008739" + ], + "longitudinal vaginal septum": [ + "HP:0008740" + ], + "vertical vaginal septum": [ + "HP:0008740" + ], + "prominent prostate median bar": [ + "HP:0008742" + ], + "coronal hypospadias": [ + "HP:0008743" + ], + "subcoronal hypospadias": [ + "HP:0008743" + ], + "abnormal aryepiglottic fold morphology": [ + "HP:0008744" + ], + "abnormal aryepiglottic fold": [ + "HP:0008744" + ], + "abnormal aryepiglottic folds": [ + "HP:0008744" + ], + "abnormality of the aryepiglottic fold": [ + "HP:0008744" + ], + "cartilaginous ossification of larynx": [ + "HP:0008747" + ], + "laryngeal hypoplasia": [ + "HP:0008749" + ], + "hypoplastic larynx": [ + "HP:0008749" + ], + "laryngeal atresia": [ + "HP:0008750" + ], + "laryngeal cleft": [ + "HP:0008751" + ], + "laryngotracheal cleft": [ + "HP:0008751" + ], + "laryngotracheoesophageal cleft i": [ + "HP:0008751" + ], + "laryngeal cartilage malformation": [ + "HP:0008752" + ], + "vocal impairment , severe , due to laryngeal cartilage abnormality": [ + "HP:0008752" + ], + "vocal impairment , severe , due to laryngeal cartilage abnormalities": [ + "HP:0008752" + ], + "aplasia of the epiglottis": [ + "HP:0008753" + ], + "absent epiglottis": [ + "HP:0008753" + ], + "laryngeal calcification": [ + "HP:0008754" + ], + "laryngeal calcifications": [ + "HP:0008754" + ], + "laryngotracheomalacia": [ + "HP:0008755" + ], + "bowing of the vocal cord": [ + "HP:0008756" + ], + "bowing of the vocal cords": [ + "HP:0008756" + ], + "unilateral vocal cord paralysis": [ + "HP:0008757" + ], + "unilateral paralysis of the vocal cord": [ + "HP:0008757" + ], + "violent behavior": [ + "HP:0008760" + ], + "violent behaviour": [ + "HP:0008760" + ], + "repetitive compulsive behavior": [ + "HP:0008762" + ], + "repetitive compulsive behaviour": [ + "HP:0008762" + ], + "no social interaction": [ + "HP:0008763" + ], + "auditory hallucination": [ + "HP:0008765" + ], + "auditory hallucinations": [ + "HP:0008765" + ], + "hallucination of sound": [ + "HP:0008765" + ], + "hallucinations of sound": [ + "HP:0008765" + ], + "hear sound": [ + "HP:0008765" + ], + "hearing sounds": [ + "HP:0008765" + ], + "self - mutilation of tongue and lip due to involuntary movement": [ + "HP:0008767" + ], + "self - mutilation of tongue and lips due to involuntary movements": [ + "HP:0008767" + ], + "inappropriate sexual behavior": [ + "HP:0008768" + ], + "inappropriate sexual behaviour": [ + "HP:0008768" + ], + "obsessive - compulsive trait": [ + "HP:0008770" + ], + "obsessive - compulsive traits": [ + "HP:0008770" + ], + "aplasia / hypoplasia of the ear": [ + "HP:0008771" + ], + "absent / small ear": [ + "HP:0008771" + ], + "absent / underdevelop ear": [ + "HP:0008771" + ], + "absent / underdeveloped ear": [ + "HP:0008771" + ], + "aplasia / hypoplasia of the external ear": [ + "HP:0008772" + ], + "absent / small external ear": [ + "HP:0008772" + ], + "absent / underdevelop external ear": [ + "HP:0008772" + ], + "absent / underdeveloped external ear": [ + "HP:0008772" + ], + "aplasia / hypoplasia of the middle ear": [ + "HP:0008773" + ], + "absent / small middle ear": [ + "HP:0008773" + ], + "absent / underdevelop middle ear": [ + "HP:0008773" + ], + "absent / underdeveloped middle ear": [ + "HP:0008773" + ], + "hypoplastic / aplastic middle ear structure": [ + "HP:0008773" + ], + "hypoplastic / aplastic middle ear structures": [ + "HP:0008773" + ], + "middle ear hypoplasia / aplasia": [ + "HP:0008773" + ], + "aplasia / hypoplasia of the inner ear": [ + "HP:0008774" + ], + "absent / small inner ear": [ + "HP:0008774" + ], + "absent / underdevelop inner ear": [ + "HP:0008774" + ], + "absent / underdeveloped inner ear": [ + "HP:0008774" + ], + "abnormal prostate morphology": [ + "HP:0008775" + ], + "abnormality of the prostate": [ + "HP:0008775" + ], + "abnormal renal artery morphology": [ + "HP:0008776" + ], + "abnormal kidney artery": [ + "HP:0008776" + ], + "abnormality of the renal artery": [ + "HP:0008776" + ], + "abnormal vocal cord morphology": [ + "HP:0008777" + ], + "abnormality of the vocal cord": [ + "HP:0008777" + ], + "abnormality of the vocal cords": [ + "HP:0008777" + ], + "congenital bilateral hip dislocation": [ + "HP:0008780" + ], + "wide proximal femoral metaphysis": [ + "HP:0008783" + ], + "wide metaphysis of innermost thighbone": [ + "HP:0008783" + ], + "wide capital femoral epiphysis": [ + "HP:0008784" + ], + "wide capital femoral epiphyses": [ + "HP:0008784" + ], + "wide end part of innermost thighbone": [ + "HP:0008784" + ], + "delay ossification of pubic ramus": [ + "HP:0008785" + ], + "delayed ossification of pubic rami": [ + "HP:0008785" + ], + "iliac crest serration": [ + "HP:0008786" + ], + "irregular lacy iliac crest": [ + "HP:0008786" + ], + "lacy appearance of iliac crest": [ + "HP:0008786" + ], + "delay pubic bone ossification": [ + "HP:0008788" + ], + "delayed pubic bone ossification": [ + "HP:0008788" + ], + "absent pubic ossification in infancy": [ + "HP:0008788" + ], + "delay maturation fo pubic bone": [ + "HP:0008788" + ], + "delayed maturation fo pubic bone": [ + "HP:0008788" + ], + "delay mineralization of pubic bone": [ + "HP:0008788" + ], + "delayed mineralization of pubic bone": [ + "HP:0008788" + ], + "cone - shaped capital femoral epiphysis": [ + "HP:0008789" + ], + "cone - shaped end part of innermost thighbone": [ + "HP:0008789" + ], + "dysplastic iliac wing": [ + "HP:0008794" + ], + "dysplastic iliac wings": [ + "HP:0008794" + ], + "externally rotate hip": [ + "HP:0008796" + ], + "externally rotated hips": [ + "HP:0008796" + ], + "early ossification of capital femoral epiphysis": [ + "HP:0008797" + ], + "early ossification of capital femoral epiphyses": [ + "HP:0008797" + ], + "widen great sciatic notch": [ + "HP:0008798" + ], + "widened greater sciatic notch": [ + "HP:0008798" + ], + "widen sacrosciatic notch": [ + "HP:0008798" + ], + "widened sacrosciatic notch": [ + "HP:0008798" + ], + "widening of the sacrosciatic notch": [ + "HP:0008798" + ], + "limited hip movement": [ + "HP:0008800" + ], + "hypoplasia of the less trochanter": [ + "HP:0008801" + ], + "hypoplasia of the lesser trochanter": [ + "HP:0008801" + ], + "less trochanter hypoplasia": [ + "HP:0008801" + ], + "lesser trochanter hypoplasia": [ + "HP:0008801" + ], + "hypoplasia of the femoral head": [ + "HP:0008802" + ], + "hypoplastic femoral head": [ + "HP:0008802" + ], + "small femoral head": [ + "HP:0008802" + ], + "small femoral heads": [ + "HP:0008802" + ], + "small head of thigh bone": [ + "HP:0008802" + ], + "obsolete narrow sacroiliac notch": [ + "HP:0008803" + ], + "broad femoral head": [ + "HP:0008804" + ], + "wide head of thigh bone": [ + "HP:0008804" + ], + "acetabular dysplasia": [ + "HP:0008807" + ], + "dysplastic acetabulae": [ + "HP:0008807" + ], + "high iliac wing": [ + "HP:0008808" + ], + "high iliac wings": [ + "HP:0008808" + ], + "narrow , high iliac wing": [ + "HP:0008808" + ], + "narrow , high iliac wings": [ + "HP:0008808" + ], + "flatten femoral head": [ + "HP:0008812" + ], + "flattened femoral head": [ + "HP:0008812" + ], + "flat head of thigh bone": [ + "HP:0008812" + ], + "flattened femoral heads": [ + "HP:0008812" + ], + "aplastic pubic bone": [ + "HP:0008817" + ], + "aplastic pubic bones": [ + "HP:0008817" + ], + "absent pubic bone": [ + "HP:0008817" + ], + "absent pubic bones": [ + "HP:0008817" + ], + "large iliac wing": [ + "HP:0008818" + ], + "large iliac wings": [ + "HP:0008818" + ], + "narrow femoral neck": [ + "HP:0008819" + ], + "narrow femoral necks": [ + "HP:0008819" + ], + "narrow neck of thigh bone": [ + "HP:0008819" + ], + "absent ossification of capital femoral epiphysis": [ + "HP:0008820" + ], + "absent ossification of femoral capital epiphysis": [ + "HP:0008820" + ], + "absent ossification of femoral capital epiphyses": [ + "HP:0008820" + ], + "hypoplastic inferior ilium": [ + "HP:0008821" + ], + "hypoplastic inferior ilia": [ + "HP:0008821" + ], + "hypoplastic ischiopubic ramus": [ + "HP:0008822" + ], + "hypoplastic ischiopubic rami": [ + "HP:0008822" + ], + "hypoplastic inferior pubic ramus": [ + "HP:0008823" + ], + "hypoplastic inferior pubic rami": [ + "HP:0008823" + ], + "hypoplastic iliac body": [ + "HP:0008824" + ], + "hypoplastic iliac bodies": [ + "HP:0008824" + ], + "small iliac body": [ + "HP:0008824" + ], + "small iliac bodies": [ + "HP:0008824" + ], + "dislocation of the femoral head": [ + "HP:0008826" + ], + "dislocate femoral head": [ + "HP:0008826" + ], + "dislocated femoral heads": [ + "HP:0008826" + ], + "dislocate head of thigh bone": [ + "HP:0008826" + ], + "dislocated head of thigh bone": [ + "HP:0008826" + ], + "delay proximal femoral epiphyseal ossification": [ + "HP:0008828" + ], + "delayed proximal femoral epiphyseal ossification": [ + "HP:0008828" + ], + "delay ossification of the proximal femoral epiphysis": [ + "HP:0008828" + ], + "delayed ossification of the proximal femoral epiphysis": [ + "HP:0008828" + ], + "delay ossification proximal femoral epiphysis": [ + "HP:0008828" + ], + "delayed ossification proximal femoral epiphyses": [ + "HP:0008828" + ], + "delay femoral head ossification": [ + "HP:0008829" + ], + "delayed femoral head ossification": [ + "HP:0008829" + ], + "delay maturation of the head of the thigh bone": [ + "HP:0008829" + ], + "delayed maturation of the head of the thigh bone": [ + "HP:0008829" + ], + "hypoplastic pubic ramus": [ + "HP:0008830" + ], + "hypoplastic pubic rami": [ + "HP:0008830" + ], + "irregular acetabular roof": [ + "HP:0008833" + ], + "multicentric femoral head ossification": [ + "HP:0008835" + ], + "stipple calcification proximal humeral epiphysis": [ + "HP:0008838" + ], + "stippled calcification proximal humeral epiphyses": [ + "HP:0008838" + ], + "speckled calcification in end part of innermost long bone of upper arm": [ + "HP:0008838" + ], + "speckled calcifications in end part of innermost long bone of upper arm": [ + "HP:0008838" + ], + "hypoplastic pelvis": [ + "HP:0008839" + ], + "hypoplastic pelvic bone": [ + "HP:0008839" + ], + "hypoplastic pelvic bones": [ + "HP:0008839" + ], + "small pelvis": [ + "HP:0008839" + ], + "hip osteoarthritis": [ + "HP:0008843" + ], + "osteoarthritis of hip": [ + "HP:0008843" + ], + "mesomelic short stature": [ + "HP:0008845" + ], + "dwarfism , short limb mesomelic": [ + "HP:0008845" + ], + "mesomelic dwarfism": [ + "HP:0008845" + ], + "short stature , disproportionate mesomelic": [ + "HP:0008845" + ], + "short stature , mesomelic": [ + "HP:0008845" + ], + "severe intrauterine growth retardation": [ + "HP:0008846" + ], + "intrauterine growth retardation , severe": [ + "HP:0008846" + ], + "severe prenatal growth deficiency": [ + "HP:0008846" + ], + "moderately short stature": [ + "HP:0008848" + ], + "moderate short stature": [ + "HP:0008848" + ], + "short stature , moderate": [ + "HP:0008848" + ], + "severe postnatal growth retardation": [ + "HP:0008850" + ], + "marked growth retardation": [ + "HP:0008850" + ], + "severe growth delay in child": [ + "HP:0008850" + ], + "severe growth delay in children": [ + "HP:0008850" + ], + "severe postnatal growth deficiency": [ + "HP:0008850" + ], + "severe postnatal growth failure": [ + "HP:0008850" + ], + "moderate postnatal growth retardation": [ + "HP:0008855" + ], + "moderate growth delay in child": [ + "HP:0008855" + ], + "moderate growth delay in children": [ + "HP:0008855" + ], + "neonatal short - trunk short stature": [ + "HP:0008857" + ], + "short - trunk dwarfism identifiable at birth": [ + "HP:0008857" + ], + "failure to thrive secondary to recurrent infection": [ + "HP:0008866" + ], + "failure to thrive secondary to recurrent infections": [ + "HP:0008866" + ], + "falter weight secondary to recurrent infection": [ + "HP:0008866" + ], + "faltering weight secondary to recurrent infections": [ + "HP:0008866" + ], + "weight falter secondary to recurrent infection": [ + "HP:0008866" + ], + "weight faltering secondary to recurrent infections": [ + "HP:0008866" + ], + "feed difficulty in infancy": [ + "HP:0008872" + ], + "feeding difficulties in infancy": [ + "HP:0008872" + ], + "disproportionate short - limb short stature": [ + "HP:0008873" + ], + "brachymelic dwarfism": [ + "HP:0008873" + ], + "disproportionate short limb dwarfism": [ + "HP:0008873" + ], + "dwarfism , short - limbed": [ + "HP:0008873" + ], + "micromelic dwarfism": [ + "HP:0008873" + ], + "short limb dwarfism": [ + "HP:0008873" + ], + "short limb dwarfism , disproportionate": [ + "HP:0008873" + ], + "short stature , disproportionate short limb": [ + "HP:0008873" + ], + "short stature , disproportionate short - limb": [ + "HP:0008873" + ], + "short - limb dwarfism": [ + "HP:0008873" + ], + "short - limbed dwarfism": [ + "HP:0008873" + ], + "mild intrauterine growth retardation": [ + "HP:0008883" + ], + "mild prenatal growth deficiency": [ + "HP:0008883" + ], + "adipose tissue loss": [ + "HP:0008887" + ], + "loss of fat tissue": [ + "HP:0008887" + ], + "severe short - limb dwarfism": [ + "HP:0008890" + ], + "postnatal growth retardation": [ + "HP:0008897" + ], + "growth delay as child": [ + "HP:0008897" + ], + "growth delay as children": [ + "HP:0008897" + ], + "growth retardation as child": [ + "HP:0008897" + ], + "growth retardation as children": [ + "HP:0008897" + ], + "postnatal growth deceleration": [ + "HP:0008897" + ], + "postnatal growth deficiency": [ + "HP:0008897" + ], + "postnatal growth failure": [ + "HP:0008897" + ], + "rhizomelia": [ + "HP:0008905" + ], + "disproportionately short upper portion of limb": [ + "HP:0008905" + ], + "rhizomelic dwarfism": [ + "HP:0008905" + ], + "rhizomelic limb shorten": [ + "HP:0008905" + ], + "rhizomelic limb shortening": [ + "HP:0008905" + ], + "rhizomelic short limb": [ + "HP:0008905" + ], + "rhizomelic short limbs": [ + "HP:0008905" + ], + "rhizomelic short stature": [ + "HP:0008905" + ], + "rhizomelic shortening": [ + "HP:0008905" + ], + "short stature , rhizomelic": [ + "HP:0008905" + ], + "symmetrical rhizomelic limb shorten": [ + "HP:0008905" + ], + "symmetrical rhizomelic limb shortening": [ + "HP:0008905" + ], + "lethal short - limbed short stature": [ + "HP:0008909" + ], + "lethal micromelic dwarfism": [ + "HP:0008909" + ], + "lethal short - limbed dwarfism": [ + "HP:0008909" + ], + "childhood - onset truncal obesity": [ + "HP:0008915" + ], + "truncal obesity apparent in childhood": [ + "HP:0008915" + ], + "neonatal short - limb short stature": [ + "HP:0008921" + ], + "dwarfism , neonatal short - limbed": [ + "HP:0008921" + ], + "neonatal short - limbed dwarfism": [ + "HP:0008921" + ], + "short limb dwarfism recognisable at birth": [ + "HP:0008921" + ], + "short limb dwarfism recognizable at birth": [ + "HP:0008921" + ], + "short - limb dwarfism identifiable at birth": [ + "HP:0008921" + ], + "short - limb dwarfism identifiable neonatally": [ + "HP:0008921" + ], + "short - limbed dwarfism identifiable at birth": [ + "HP:0008921" + ], + "childhood - onset short - trunk short stature": [ + "HP:0008922" + ], + "disproportionate short - trunk short stature , identifiable in childhood": [ + "HP:0008922" + ], + "short - trunk dwarfism identifiable during childhood": [ + "HP:0008922" + ], + "asymmetric short stature": [ + "HP:0008929" + ], + "generalize neonatal hypotonia": [ + "HP:0008935" + ], + "generalized neonatal hypotonia": [ + "HP:0008935" + ], + "generalise low muscle tone in neonate": [ + "HP:0008935" + ], + "generalised low muscle tone in neonate": [ + "HP:0008935" + ], + "generalise neonatal hypotonia": [ + "HP:0008935" + ], + "generalised neonatal hypotonia": [ + "HP:0008935" + ], + "generalize low muscle tone in neonate": [ + "HP:0008935" + ], + "generalized low muscle tone in neonate": [ + "HP:0008935" + ], + "hypotonia , neonatal , generalise": [ + "HP:0008935" + ], + "hypotonia , neonatal , generalised": [ + "HP:0008935" + ], + "hypotonia , neonatal , generalize": [ + "HP:0008935" + ], + "hypotonia , neonatal , generalized": [ + "HP:0008935" + ], + "muscular hypotonia of the trunk": [ + "HP:0008936" + ], + "axial hypotonia": [ + "HP:0008936" + ], + "low muscle tone in trunk": [ + "HP:0008936" + ], + "truncal hypotonia": [ + "HP:0008936" + ], + "generalize lymphadenopathy": [ + "HP:0008940" + ], + "generalized lymphadenopathy": [ + "HP:0008940" + ], + "generalise lymphadenopathy": [ + "HP:0008940" + ], + "generalised lymphadenopathy": [ + "HP:0008940" + ], + "generalised swelling of lymph node": [ + "HP:0008940" + ], + "generalised swelling of lymph nodes": [ + "HP:0008940" + ], + "generalize swelling of lymph node": [ + "HP:0008940" + ], + "generalized swelling of lymph nodes": [ + "HP:0008940" + ], + "swollen lymph node affect all region of the body": [ + "HP:0008940" + ], + "swollen lymph nodes affecting all regions of the body": [ + "HP:0008940" + ], + "acute rhabdomyolysis": [ + "HP:0008942" + ], + "rhabdomyolysis , acute": [ + "HP:0008942" + ], + "distal low limb amyotrophy": [ + "HP:0008944" + ], + "distal lower limb amyotrophy": [ + "HP:0008944" + ], + "low leg amyotrophy": [ + "HP:0008944" + ], + "lower leg amyotrophy": [ + "HP:0008944" + ], + "low limb atrophy": [ + "HP:0008944" + ], + "lower limb atrophy": [ + "HP:0008944" + ], + "low limb degeneration": [ + "HP:0008944" + ], + "lower limb degeneration": [ + "HP:0008944" + ], + "low limb muscle hypotrophy": [ + "HP:0008944" + ], + "lower limb muscle hypotrophy": [ + "HP:0008944" + ], + "muscle atrophy , low limb , distal": [ + "HP:0008944" + ], + "muscle atrophy , lower limb , distal": [ + "HP:0008944" + ], + "loss of ability to walk in early childhood": [ + "HP:0008945" + ], + "pelvic girdle amyotrophy": [ + "HP:0008946" + ], + "hip girdle amyotrophy": [ + "HP:0008946" + ], + "infantile muscular hypotonia": [ + "HP:0008947" + ], + "decreased muscle tone in infant": [ + "HP:0008947" + ], + "hypotonia early": [ + "HP:0008947" + ], + "hypotonia in infancy": [ + "HP:0008947" + ], + "hypotonia , early": [ + "HP:0008947" + ], + "infantile hypotonia": [ + "HP:0008947" + ], + "proximal upper limb amyotrophy": [ + "HP:0008948" + ], + "proximal muscle atrophy in upper limb": [ + "HP:0008948" + ], + "proximal muscle atrophy in upper limbs": [ + "HP:0008948" + ], + "proximal upper limb muscle atrophy": [ + "HP:0008948" + ], + "shoulder muscle hypoplasia": [ + "HP:0008952" + ], + "underdeveloped shoulder muscle": [ + "HP:0008952" + ], + "pectoralis major hypoplasia": [ + "HP:0008953" + ], + "pectoralis major muscle hypoplasia": [ + "HP:0008953" + ], + "intrinsic hand muscle atrophy": [ + "HP:0008954" + ], + "progressive distal muscular atrophy": [ + "HP:0008955" + ], + "proximal low limb amyotrophy": [ + "HP:0008956" + ], + "proximal lower limb amyotrophy": [ + "HP:0008956" + ], + "amyotrophy involve the thigh": [ + "HP:0008956" + ], + "amyotrophy involving the thigh": [ + "HP:0008956" + ], + "amyotrophy of the thigh musculature": [ + "HP:0008956" + ], + "proximal low limb muscle atrophy": [ + "HP:0008956" + ], + "proximal lower limb muscle atrophy": [ + "HP:0008956" + ], + "thigh muscle atrophy": [ + "HP:0008956" + ], + "wasting of thigh muscle": [ + "HP:0008956" + ], + "distal upper limb muscle weakness": [ + "HP:0008959" + ], + "calf muscle hypoplasia": [ + "HP:0008962" + ], + "hypoplastic calf muscle": [ + "HP:0008962" + ], + "hypoplastic calf muscles": [ + "HP:0008962" + ], + "underdeveloped calf muscle": [ + "HP:0008962" + ], + "underdeveloped calf muscles": [ + "HP:0008962" + ], + "tibialis muscle weakness": [ + "HP:0008963" + ], + "nonprogressive muscular atrophy": [ + "HP:0008964" + ], + "exercise - induced muscle stiffness": [ + "HP:0008967" + ], + "muscle stiffness with exercise": [ + "HP:0008967" + ], + "muscle stiffness , exercise - induced": [ + "HP:0008967" + ], + "muscle hypertrophy of the low extremity": [ + "HP:0008968" + ], + "muscle hypertrophy of the lower extremities": [ + "HP:0008968" + ], + "leg muscle stiffness": [ + "HP:0008969" + ], + "scapulohumeral muscular dystrophy": [ + "HP:0008970" + ], + "decreased activity of mitochondrial respiratory chain": [ + "HP:0008972" + ], + "decreased activity of mitochondrial - encoded respiratory chain complex": [ + "HP:0008972" + ], + "decreased activities of mitochondrial - encoded respiratory chain complexes": [ + "HP:0008972" + ], + "decreased activity of mitochondrial respiratory complex": [ + "HP:0008972" + ], + "decreased activity of mitochondrial respiratory complexes": [ + "HP:0008972" + ], + "necrotizing myopathy": [ + "HP:0008978" + ], + "calf muscle hypertrophy": [ + "HP:0008981" + ], + "calf hypertrophy": [ + "HP:0008981" + ], + "increase size of calf muscle": [ + "HP:0008981" + ], + "increased size of calf muscles": [ + "HP:0008981" + ], + "muscular hypertrophy of the calf muscle": [ + "HP:0008981" + ], + "muscular hypertrophy of the calf muscles": [ + "HP:0008981" + ], + "neck muscle hypoplasia": [ + "HP:0008984" + ], + "decreased size of neck muscle": [ + "HP:0008984" + ], + "deficiency of neck muscle": [ + "HP:0008984" + ], + "hypotrophic neck muscle": [ + "HP:0008984" + ], + "small neck muscle": [ + "HP:0008984" + ], + "underdevelopment of neck muscle": [ + "HP:0008984" + ], + "increase intramuscular fat": [ + "HP:0008985" + ], + "increased intramuscular fat": [ + "HP:0008985" + ], + "increase im fat": [ + "HP:0008985" + ], + "increased im fat": [ + "HP:0008985" + ], + "agenesis of the diaphragm": [ + "HP:0008986" + ], + "absent diaphragm": [ + "HP:0008986" + ], + "agenesis of diaphragm": [ + "HP:0008986" + ], + "pelvic girdle muscle atrophy": [ + "HP:0008988" + ], + "pelvic girdle muscle waste": [ + "HP:0008988" + ], + "pelvic girdle muscle wasting": [ + "HP:0008988" + ], + "exercise - induced leg cramp": [ + "HP:0008991" + ], + "exercise - induced leg cramps": [ + "HP:0008991" + ], + "increase intraabdominal fat": [ + "HP:0008993" + ], + "increased intraabdominal fat": [ + "HP:0008993" + ], + "proximal muscle weakness in low limb": [ + "HP:0008994" + ], + "proximal muscle weakness in lower limbs": [ + "HP:0008994" + ], + "muscle weakness , proximal , low limb": [ + "HP:0008994" + ], + "muscle weakness , proximal , lower limbs": [ + "HP:0008994" + ], + "proximal muscle weakness in upper limb": [ + "HP:0008997" + ], + "proximal muscle weakness in upper limbs": [ + "HP:0008997" + ], + "pectoralis hypoplasia": [ + "HP:0008998" + ], + "hypoplastic pectoral muscle": [ + "HP:0008998" + ], + "small pec muscle": [ + "HP:0008998" + ], + "underdeveloped pec muscle": [ + "HP:0008998" + ], + "loss of truncal subcutaneous adipose tissue": [ + "HP:0009002" + ], + "loss of fat tissue in trunk": [ + "HP:0009002" + ], + "loss of subcutaneous truncal adipose tissue": [ + "HP:0009002" + ], + "loss of truncal adipose tissue": [ + "HP:0009002" + ], + "increase subcutaneous truncal adipose tissue": [ + "HP:0009003" + ], + "increased subcutaneous truncal adipose tissue": [ + "HP:0009003" + ], + "increase fat below the skin in trunk": [ + "HP:0009003" + ], + "increased fat below the skin in trunk": [ + "HP:0009003" + ], + "hypoplasia of the musculature": [ + "HP:0009004" + ], + "muscle hypoplasia": [ + "HP:0009004" + ], + "poorly develop skeletal musculature": [ + "HP:0009004" + ], + "poorly developed skeletal musculature": [ + "HP:0009004" + ], + "underdeveloped muscle": [ + "HP:0009004" + ], + "underdeveloped muscles": [ + "HP:0009004" + ], + "weakness of the intrinsic hand muscle": [ + "HP:0009005" + ], + "weakness of the intrinsic hand muscles": [ + "HP:0009005" + ], + "intrinsic hand muscle weakness": [ + "HP:0009005" + ], + "biceps hypoplasia": [ + "HP:0009007" + ], + "hypoplastic biceps": [ + "HP:0009007" + ], + "underdeveloped biceps": [ + "HP:0009007" + ], + "hypoplasia of serratus anterior muscle": [ + "HP:0009011" + ], + "congenital absence of gluteal muscle": [ + "HP:0009013" + ], + "congenital absence of gluteal muscles": [ + "HP:0009013" + ], + "upper limb muscle hypoplasia": [ + "HP:0009016" + ], + "underdevelopment of upper limb muscle": [ + "HP:0009016" + ], + "underdevelopment of upper limb muscles": [ + "HP:0009016" + ], + "loss of gluteal subcutaneous adipose tissue": [ + "HP:0009017" + ], + "loss of fat tissue below the skin in glut": [ + "HP:0009017" + ], + "loss of fat tissue below the skin in gluts": [ + "HP:0009017" + ], + "progressive loss of facial adipose tissue": [ + "HP:0009019" + ], + "atrophy of facial adipose tissue": [ + "HP:0009019" + ], + "facial fat atrophy": [ + "HP:0009019" + ], + "facial fat wasting": [ + "HP:0009019" + ], + "loss of subcutaneous adipose tissue from face , progressive": [ + "HP:0009019" + ], + "progressive loss of facial fat": [ + "HP:0009019" + ], + "progressive loss of facial subcutaneous adipose tissue": [ + "HP:0009019" + ], + "progressive loss of subcutaneous adipose tissue from face": [ + "HP:0009019" + ], + "exercise - induced muscle fatigue": [ + "HP:0009020" + ], + "abdominal wall muscle weakness": [ + "HP:0009023" + ], + "lax abdominal musculature": [ + "HP:0009023" + ], + "increase connective tissue": [ + "HP:0009025" + ], + "increased connective tissue": [ + "HP:0009025" + ], + "hypoplasia of latissimus dorsi muscle": [ + "HP:0009026" + ], + "foot dorsiflexor weakness": [ + "HP:0009027" + ], + "foot drop": [ + "HP:0009027" + ], + "foot extensor weakness": [ + "HP:0009027" + ], + "footdrop": [ + "HP:0009027" + ], + "inability to heel walk": [ + "HP:0009027" + ], + "inability to walk on heel": [ + "HP:0009027" + ], + "inability to walk on heels": [ + "HP:0009027" + ], + "generalized weakness of limb muscle": [ + "HP:0009028" + ], + "generalized weakness of limb muscles": [ + "HP:0009028" + ], + "generalised weakness of limb muscle": [ + "HP:0009028" + ], + "generalised weakness of limb muscles": [ + "HP:0009028" + ], + "amyotrophy of ankle musculature": [ + "HP:0009031" + ], + "segmental spinal muscular atrophy": [ + "HP:0009037" + ], + "mark muscular hypertrophy": [ + "HP:0009042" + ], + "marked muscular hypertrophy": [ + "HP:0009042" + ], + "obsolete hypoplasia of deltoid muscle": [ + "HP:0009044" + ], + "exercise - induced rhabdomyolysis": [ + "HP:0009045" + ], + "rhabdomyolysis with exercise": [ + "HP:0009045" + ], + "difficulty run": [ + "HP:0009046" + ], + "difficulty running": [ + "HP:0009046" + ], + "peroneal muscle atrophy": [ + "HP:0009049" + ], + "peroneal atrophy": [ + "HP:0009049" + ], + "quadriceps muscle atrophy": [ + "HP:0009050" + ], + "wasting of quad muscle": [ + "HP:0009050" + ], + "wasting of quad muscles": [ + "HP:0009050" + ], + "increase muscle glycogen content": [ + "HP:0009051" + ], + "increased muscle glycogen content": [ + "HP:0009051" + ], + "distal low limb muscle weakness": [ + "HP:0009053" + ], + "distal lower limb muscle weakness": [ + "HP:0009053" + ], + "distal muscle weakness in low limb": [ + "HP:0009053" + ], + "distal muscle weakness in lower limbs": [ + "HP:0009053" + ], + "muscle weakness , low limb , distal": [ + "HP:0009053" + ], + "muscle weakness , lower limb , distal": [ + "HP:0009053" + ], + "scapuloperoneal myopathy": [ + "HP:0009054" + ], + "generalize limb muscle atrophy": [ + "HP:0009055" + ], + "generalized limb muscle atrophy": [ + "HP:0009055" + ], + "generalise limb muscle atrophy": [ + "HP:0009055" + ], + "generalised limb muscle atrophy": [ + "HP:0009055" + ], + "generalised muscle atrophy , proximal and distal": [ + "HP:0009055" + ], + "generalised muscle waste": [ + "HP:0009055" + ], + "generalised muscle wasting": [ + "HP:0009055" + ], + "generalize muscle atrophy , proximal and distal": [ + "HP:0009055" + ], + "generalized muscle atrophy , proximal and distal": [ + "HP:0009055" + ], + "generalize muscle waste": [ + "HP:0009055" + ], + "generalized muscle wasting": [ + "HP:0009055" + ], + "loss of subcutaneous adipose tissue from upper limb": [ + "HP:0009056" + ], + "loss of subcutaneous adipose tissue from upper limbs": [ + "HP:0009056" + ], + "loss of fat tissue below the skin from upper limb": [ + "HP:0009056" + ], + "loss of fat tissue below the skin from upper limbs": [ + "HP:0009056" + ], + "increase muscle lipid content": [ + "HP:0009058" + ], + "increased muscle lipid content": [ + "HP:0009058" + ], + "fat accumulation in muscle fiber": [ + "HP:0009058" + ], + "fat accumulation in muscle fibers": [ + "HP:0009058" + ], + "fat accumulation in muscle fibre": [ + "HP:0009058" + ], + "fat accumulation in muscle fibres": [ + "HP:0009058" + ], + "fat deposit in muscle fiber": [ + "HP:0009058" + ], + "fat deposits in muscle fibers": [ + "HP:0009058" + ], + "fat deposit in muscle fibre": [ + "HP:0009058" + ], + "fat deposits in muscle fibres": [ + "HP:0009058" + ], + "lipid accumulation in skeletal muscle": [ + "HP:0009058" + ], + "muscle lipidosis": [ + "HP:0009058" + ], + "skeletal muscle lipid accumulation": [ + "HP:0009058" + ], + "congenital generalize lipodystrophy": [ + "HP:0009059" + ], + "congenital generalized lipodystrophy": [ + "HP:0009059" + ], + "congenital generalise lipodystrophy": [ + "HP:0009059" + ], + "congenital generalised lipodystrophy": [ + "HP:0009059" + ], + "scapular muscle atrophy": [ + "HP:0009060" + ], + "infantile axial hypotonia": [ + "HP:0009062" + ], + "hypotonia , axial , in infancy": [ + "HP:0009062" + ], + "progressive distal muscle weakness": [ + "HP:0009063" + ], + "muscle weakness , distal , progressive": [ + "HP:0009063" + ], + "muscle weakness , progressive , distal": [ + "HP:0009063" + ], + "generalize lipodystrophy": [ + "HP:0009064" + ], + "generalized lipodystrophy": [ + "HP:0009064" + ], + "generalise lipodystrophy": [ + "HP:0009064" + ], + "generalised lipodystrophy": [ + "HP:0009064" + ], + "lipodystrophy , generalise": [ + "HP:0009064" + ], + "lipodystrophy , generalised": [ + "HP:0009064" + ], + "lipodystrophy , generalize": [ + "HP:0009064" + ], + "lipodystrophy , generalized": [ + "HP:0009064" + ], + "progressive spinal muscular atrophy": [ + "HP:0009067" + ], + "progressive spinal muscle degeneration": [ + "HP:0009067" + ], + "progressive spinal muscle waste": [ + "HP:0009067" + ], + "progressive spinal muscle wasting": [ + "HP:0009067" + ], + "lethal infantile mitochondrial myopathy": [ + "HP:0009069" + ], + "inflammatory myopathy": [ + "HP:0009071" + ], + "decrease achilles reflex": [ + "HP:0009072" + ], + "decreased achilles reflex": [ + "HP:0009072" + ], + "hyporeflexia at ankle joint": [ + "HP:0009072" + ], + "hyporeflexia at ankle joints": [ + "HP:0009072" + ], + "progressive proximal muscle weakness": [ + "HP:0009073" + ], + "muscle weakness , progressive , proximal": [ + "HP:0009073" + ], + "weakness of long finger extensor muscle": [ + "HP:0009077" + ], + "weakness of long finger extensor muscles": [ + "HP:0009077" + ], + "midline notch of upper alveolar ridge": [ + "HP:0009084" + ], + "midline cleft of maxillary alveolar process": [ + "HP:0009084" + ], + "midline cleft of upper alveolar ridge": [ + "HP:0009084" + ], + "midline notch of maxillary alveolar process": [ + "HP:0009084" + ], + "midline notch of maxillary alveolar ridge": [ + "HP:0009084" + ], + "midline notch of upper gum ridge": [ + "HP:0009084" + ], + "alveolar ridge overgrowth": [ + "HP:0009085" + ], + "alveolar ridge excess": [ + "HP:0009085" + ], + "enlarge alveolar ridge": [ + "HP:0009085" + ], + "enlarged alveolar ridge": [ + "HP:0009085" + ], + "hyperplasia of alveolar process of jaw": [ + "HP:0009085" + ], + "hyperplasia of alveolar ridge": [ + "HP:0009085" + ], + "hypertrophy alveolar ridge": [ + "HP:0009085" + ], + "hypertrophied alveolar ridge": [ + "HP:0009085" + ], + "increase size of alveolar ridge": [ + "HP:0009085" + ], + "increased size of alveolar ridge": [ + "HP:0009085" + ], + "increase size of gum ridge": [ + "HP:0009085", + "HP:0009092" + ], + "increased size of gum ridge": [ + "HP:0009085" + ], + "overgrowth of alveolar ridge": [ + "HP:0009085" + ], + "overgrowth of gum ridge": [ + "HP:0009085" + ], + "thick alveolar ridge": [ + "HP:0009085" + ], + "thick alveolar ridges": [ + "HP:0009085" + ], + "thicken alveolar ridge": [ + "HP:0009085" + ], + "thickened alveolar ridges": [ + "HP:0009085" + ], + "posteriorly place tongue": [ + "HP:0009087" + ], + "posteriorly placed tongue": [ + "HP:0009087" + ], + "speech articulation difficulty": [ + "HP:0009088" + ], + "speech articulation difficulties": [ + "HP:0009088" + ], + "obsolete facial diplegic appearance": [ + "HP:0009090" + ], + "progressive alveolar ridge hypertropy": [ + "HP:0009092" + ], + "increase overgrowth of gum ridge": [ + "HP:0009092" + ], + "increasing overgrowth of gum ridge": [ + "HP:0009092" + ], + "increasing size of gum ridge": [ + "HP:0009092" + ], + "progressive hypertrophy of alveolar process of jaw": [ + "HP:0009092" + ], + "cleft low alveolar ridge": [ + "HP:0009094" + ], + "cleft lower alveolar ridge": [ + "HP:0009094" + ], + "cleft of low alveolar process": [ + "HP:0009094" + ], + "cleft of lower alveolar process": [ + "HP:0009094" + ], + "cleft of low gingiva": [ + "HP:0009094" + ], + "cleft of lower gingiva": [ + "HP:0009094" + ], + "cleft of low gum ridge": [ + "HP:0009094" + ], + "cleft of lower gum ridge": [ + "HP:0009094" + ], + "cleft of mandibular alveolar process": [ + "HP:0009094" + ], + "cleft of mandibular gingiva": [ + "HP:0009094" + ], + "notch of low alveolar process": [ + "HP:0009094" + ], + "notch of lower alveolar process": [ + "HP:0009094" + ], + "notch of low alveolar ridge": [ + "HP:0009094" + ], + "notch of lower alveolar ridge": [ + "HP:0009094" + ], + "notch of low gum ridge": [ + "HP:0009094" + ], + "notch of lower gum ridge": [ + "HP:0009094" + ], + "notch of mandibular alveolar process": [ + "HP:0009094" + ], + "notch of mandibular alveolar ridge": [ + "HP:0009094" + ], + "chronic oral candidiasis": [ + "HP:0009098" + ], + "chronic oral thrush": [ + "HP:0009098" + ], + "median cleft palate": [ + "HP:0009099" + ], + "central cleft palate": [ + "HP:0009099" + ], + "midline cleft palate": [ + "HP:0009099" + ], + "thick anterior alveolar ridge": [ + "HP:0009100" + ], + "thick anterior alveolar ridges": [ + "HP:0009100" + ], + "thick anterior alveolar process of jaw": [ + "HP:0009100" + ], + "submucous cleft lip": [ + "HP:0009101" + ], + "submucous labial cleft": [ + "HP:0009101" + ], + "anterior open - bite malocclusion": [ + "HP:0009102" + ], + "absence of overlap of anterior upper and low teeth": [ + "HP:0009102" + ], + "absence of overlap of anterior upper and lower teeth": [ + "HP:0009102" + ], + "anterior open bite": [ + "HP:0009102" + ], + "anterior open bite between upper and low teeth": [ + "HP:0009102" + ], + "anterior open bite between upper and lower teeth": [ + "HP:0009102" + ], + "anterior openbite": [ + "HP:0009102" + ], + "apertognathia malocclusion": [ + "HP:0009102" + ], + "gap between upper and low front teeth when bite": [ + "HP:0009102" + ], + "gap between upper and lower front teeth when biting": [ + "HP:0009102" + ], + "aplasia / hypoplasia involve the pelvis": [ + "HP:0009103" + ], + "aplasia / hypoplasia involving the pelvis": [ + "HP:0009103" + ], + "absent / small pelvis": [ + "HP:0009103" + ], + "absent / underdevelop pelvis": [ + "HP:0009103" + ], + "absent / underdeveloped pelvis": [ + "HP:0009103" + ], + "aplasia / hypoplasia of the pubic bone": [ + "HP:0009104" + ], + "absent / small pubic bone": [ + "HP:0009104" + ], + "absent / small pubic bones": [ + "HP:0009104" + ], + "absent / underdevelop pubic bone": [ + "HP:0009104" + ], + "absent / underdeveloped pubic bones": [ + "HP:0009104" + ], + "hypoplastic / aplastic pubic bone": [ + "HP:0009104" + ], + "hypoplastic / aplastic pubic bones": [ + "HP:0009104" + ], + "abnormal ossification of the pubic bone": [ + "HP:0009105" + ], + "abnormal maturation of the pubic bone": [ + "HP:0009105" + ], + "abnormal pelvis bone ossification": [ + "HP:0009106" + ], + "abnormal maturation of the pelvis bone": [ + "HP:0009106" + ], + "abnormal ossification involve the bone of the pelvis": [ + "HP:0009106" + ], + "abnormal ossification involving the bones of the pelvis": [ + "HP:0009106" + ], + "abnormal ossification involve the femoral head and neck": [ + "HP:0009107" + ], + "abnormal ossification involving the femoral head and neck": [ + "HP:0009107" + ], + "abnormal maturation of thigh bone head and neck": [ + "HP:0009107" + ], + "aplasia / hypoplasia involve the femoral head and neck": [ + "HP:0009108" + ], + "aplasia / hypoplasia involving the femoral head and neck": [ + "HP:0009108" + ], + "absent / small head and neck of thighbone": [ + "HP:0009108" + ], + "absent / underdeveloped head and neck of thighbone": [ + "HP:0009108" + ], + "denervation of the diaphragm": [ + "HP:0009109" + ], + "diaphragmatic eventration": [ + "HP:0009110" + ], + "eventration of the diaphragm": [ + "HP:0009110" + ], + "aplasia of the left hemidiaphragm": [ + "HP:0009112" + ], + "absent leave hemidiaphragm": [ + "HP:0009112" + ], + "absent left hemidiaphragm": [ + "HP:0009112" + ], + "leave diaphragmatic hernia": [ + "HP:0009112" + ], + "left diaphragmatic hernia": [ + "HP:0009112" + ], + "diaphragmatic weakness": [ + "HP:0009113" + ], + "diaphragmatic paraparesis": [ + "HP:0009113" + ], + "diminish diaphragmatic motion": [ + "HP:0009113" + ], + "diminished diaphragmatic motion": [ + "HP:0009113" + ], + "weak diaphragm": [ + "HP:0009113" + ], + "aplasia / hypoplasia involve the skeleton": [ + "HP:0009115" + ], + "aplasia / hypoplasia involving the skeleton": [ + "HP:0009115" + ], + "absent / small skeleton": [ + "HP:0009115" + ], + "absent / underdevelop skeleton": [ + "HP:0009115" + ], + "absent / underdeveloped skeleton": [ + "HP:0009115" + ], + "aplasia / hypoplasia involve bone of the skull": [ + "HP:0009116" + ], + "aplasia / hypoplasia involving bones of the skull": [ + "HP:0009116" + ], + "aplasia / hypoplasia of the maxilla": [ + "HP:0009117" + ], + "underdevelopment of maxilla": [ + "HP:0009117" + ], + "underdevelopment of upper jaw bone": [ + "HP:0009117" + ], + "underdevelopment of upper jaw bones": [ + "HP:0009117" + ], + "aplasia / hypoplasia of the mandible": [ + "HP:0009118" + ], + "aplasia / hypoplasia of the frontal sinus": [ + "HP:0009119" + ], + "aplasia / hypoplasia of the frontal sinuses": [ + "HP:0009119" + ], + "abnormally small frontal sinus": [ + "HP:0009119" + ], + "aplasia / hypoplasia involve the sinus": [ + "HP:0009120" + ], + "aplasia / hypoplasia involving the sinuses": [ + "HP:0009120" + ], + "abnormal axial skeleton morphology": [ + "HP:0009121" + ], + "abnormality of the axial skeleton": [ + "HP:0009121" + ], + "aplasia / hypoplasia affect bone of the axial skeleton": [ + "HP:0009122" + ], + "aplasia / hypoplasia affecting bones of the axial skeleton": [ + "HP:0009122" + ], + "mixed hypo - and hyperpigmentation of the skin": [ + "HP:0009123" + ], + "abnormal adipose tissue morphology": [ + "HP:0009124" + ], + "abnormality of adipose tissue": [ + "HP:0009124" + ], + "abnormality of fat tissue": [ + "HP:0009124" + ], + "abnormality of fatty tissue": [ + "HP:0009124" + ], + "lipodystrophy": [ + "HP:0009125" + ], + "inability to make and keep healthy fat tissue": [ + "HP:0009125" + ], + "increase adipose tissue": [ + "HP:0009126" + ], + "increased adipose tissue": [ + "HP:0009126" + ], + "increase fat tissue": [ + "HP:0009126" + ], + "increased fat tissue": [ + "HP:0009126" + ], + "abnormality of the musculature of the limb": [ + "HP:0009127" + ], + "abnormality of the musculature of the limbs": [ + "HP:0009127" + ], + "abnormal limb muscle": [ + "HP:0009127" + ], + "abnormal limb muscles": [ + "HP:0009127" + ], + "muscle issue in the arm and / or leg": [ + "HP:0009127" + ], + "muscle issues in the arms and / or legs": [ + "HP:0009127" + ], + "aplasia / hypoplasia involve the musculature of the extremity": [ + "HP:0009128" + ], + "aplasia / hypoplasia involving the musculature of the extremities": [ + "HP:0009128" + ], + "absent / small muscle of extremity": [ + "HP:0009128" + ], + "absent / small muscles of extremities": [ + "HP:0009128" + ], + "absent / underdevelop muscle of extremity": [ + "HP:0009128" + ], + "absent / underdeveloped muscles of extremities": [ + "HP:0009128" + ], + "upper limb amyotrophy": [ + "HP:0009129" + ], + "amyotrophy involve the upper limb": [ + "HP:0009129" + ], + "amyotrophy involving the upper limbs": [ + "HP:0009129" + ], + "hand muscle atrophy": [ + "HP:0009130" + ], + "amyotrophy involve the musculature of the hand": [ + "HP:0009130" + ], + "amyotrophy involving the musculature of the hand": [ + "HP:0009130" + ], + "amyotrophy of hand muscle": [ + "HP:0009130" + ], + "amyotrophy of hand muscles": [ + "HP:0009130" + ], + "hand muscle degeneration": [ + "HP:0009130" + ], + "hand muscle wasting": [ + "HP:0009130" + ], + "hand muscle wasting , bilateral": [ + "HP:0009130" + ], + "abnormality of the musculature of the thorax": [ + "HP:0009131" + ], + "abnormal tarsal bone mineral density": [ + "HP:0009132" + ], + "abnormality of bone mineral density involve tarsal bone": [ + "HP:0009132" + ], + "abnormality of bone mineral density involving tarsal bones": [ + "HP:0009132" + ], + "osteolysis involve bone of the foot": [ + "HP:0009134" + ], + "osteolysis involving bones of the feet": [ + "HP:0009134" + ], + "duplication involve bone of the foot": [ + "HP:0009136" + ], + "duplication involving bones of the feet": [ + "HP:0009136" + ], + "synostosis involve bone of the low limb": [ + "HP:0009138" + ], + "synostosis involving bones of the lower limbs": [ + "HP:0009138" + ], + "fusion involve the bone of the low limb": [ + "HP:0009138" + ], + "fusion involving the bones of the lower limbs": [ + "HP:0009138" + ], + "osteolysis involve bone of the low limb": [ + "HP:0009139" + ], + "osteolysis involving bones of the lower limbs": [ + "HP:0009139" + ], + "synostosis involve bone of the foot": [ + "HP:0009140" + ], + "synostosis involving bones of the feet": [ + "HP:0009140" + ], + "fusion involve the bone of the foot": [ + "HP:0009140" + ], + "fusion involving the bones of the feet": [ + "HP:0009140" + ], + "depletion of mitochondrial dna in muscle tissue": [ + "HP:0009141" + ], + "depletion of mitochondrial dna in skeletal muscle tissue": [ + "HP:0009141" + ], + "duplication of bone involve the upper extremity": [ + "HP:0009142" + ], + "duplication of bones involving the upper extremities": [ + "HP:0009142" + ], + "supernumerary bone of the axial skeleton": [ + "HP:0009144" + ], + "supernumerary bones of the axial skeleton": [ + "HP:0009144" + ], + "abnormal cerebral artery morphology": [ + "HP:0009145" + ], + "abnormality of cerebral artery": [ + "HP:0009145" + ], + "abnormality of the cerebral artery": [ + "HP:0009145" + ], + "abnormality of the cerebral arteries": [ + "HP:0009145" + ], + "enlarged epiphysis of the distal phalanx of the 5th finger": [ + "HP:0009147" + ], + "enlarged end part of the outermost bone of little finger": [ + "HP:0009147" + ], + "enlarged end part of the outermost bone of pinkie finger": [ + "HP:0009147" + ], + "enlarged end part of the outermost bone of pinky finger": [ + "HP:0009147" + ], + "small epiphysis of the distal phalanx of the 5th finger": [ + "HP:0009148" + ], + "small end part of the outermost bone of little finger": [ + "HP:0009148" + ], + "small end part of the outermost bone of pinkie finger": [ + "HP:0009148" + ], + "small end part of the outermost bone of pinky finger": [ + "HP:0009148" + ], + "triangular epiphysis of the distal phalanx of the 5th finger": [ + "HP:0009149" + ], + "delta - shaped epiphysis of the distal phalanx of the 5th finger": [ + "HP:0009149" + ], + "triangular end part of the outermost bone of little finger": [ + "HP:0009149" + ], + "triangular end part of the outermost bone of pinkie finger": [ + "HP:0009149" + ], + "triangular end part of the outermost bone of pinky finger": [ + "HP:0009149" + ], + "abnormality of the proximal phalanx of the 5th finger": [ + "HP:0009150" + ], + "abnormality of the innermost bone little finger": [ + "HP:0009150" + ], + "abnormality of the innermost bone pinkie finger": [ + "HP:0009150" + ], + "abnormality of the innermost bone pinky finger": [ + "HP:0009150" + ], + "abnormality of the epiphysis of the 5th finger": [ + "HP:0009152" + ], + "abnormality of the epiphyses of the 5th finger": [ + "HP:0009152" + ], + "abnormality of end part of little finger bone": [ + "HP:0009152" + ], + "abnormality of end part of pinkie finger bone": [ + "HP:0009152" + ], + "abnormality of end part of pinky finger bone": [ + "HP:0009152" + ], + "abnormality of the epiphysis of the proximal phalanx of the 5th finger": [ + "HP:0009153" + ], + "abnormality of end part of the innermost bone of little finger": [ + "HP:0009153" + ], + "abnormality of end part of the innermost bone of pinkie finger": [ + "HP:0009153" + ], + "abnormality of end part of the innermost bone of pinky finger": [ + "HP:0009153" + ], + "triangular epiphysis of the proximal phalanx of the 5th finger": [ + "HP:0009154" + ], + "delta - shaped epiphysis of the proximal phalanx of the 5th finger": [ + "HP:0009154" + ], + "triangular end part of the innermost bone of little finger": [ + "HP:0009154" + ], + "triangular end part of the innermost bone of pinkie finger": [ + "HP:0009154" + ], + "triangular end part of the innermost bone of pinky finger": [ + "HP:0009154" + ], + "cone - shaped epiphysis of the proximal phalanx of the 5th finger": [ + "HP:0009155" + ], + "angel - shaped epiphysis of the proximal phalanx of the 5th finger": [ + "HP:0009155" + ], + "cone - shaped end part of the innermost bone of little finger": [ + "HP:0009155" + ], + "cone - shaped end part of the innermost bone of pinkie finger": [ + "HP:0009155" + ], + "cone - shaped end part of the innermost bone of pinky finger": [ + "HP:0009155" + ], + "cone - shaped epiphysis of the proximal phalanx of the little finger": [ + "HP:0009155" + ], + "ivory epiphysis of the proximal phalanx of the 5th finger": [ + "HP:0009157" + ], + "increase bone density of end part of the innermost bone of little finger": [ + "HP:0009157" + ], + "increased bone density of end part of the innermost bone of little finger": [ + "HP:0009157" + ], + "increase bone density of end part of the innermost bone of pinkie finger": [ + "HP:0009157" + ], + "increased bone density of end part of the innermost bone of pinkie finger": [ + "HP:0009157" + ], + "increase bone density of end part of the innermost bone of pinky finger": [ + "HP:0009157" + ], + "increased bone density of end part of the innermost bone of pinky finger": [ + "HP:0009157" + ], + "ivory epiphysis of the proximal phalanx of the little finger": [ + "HP:0009157" + ], + "enlarged epiphysis of the proximal phalanx of the 5th finger": [ + "HP:0009158" + ], + "enlarged end part of the innermost bone of little finger": [ + "HP:0009158" + ], + "enlarged end part of the innermost bone of pinkie finger": [ + "HP:0009158" + ], + "enlarged end part of the innermost bone of pinky finger": [ + "HP:0009158" + ], + "small epiphysis of the proximal phalanx of the 5th finger": [ + "HP:0009159" + ], + "small end part of the innermost bone of little finger": [ + "HP:0009159" + ], + "small end part of the innermost bone of pinkie finger": [ + "HP:0009159" + ], + "small end part of the innermost bone of pinky finger": [ + "HP:0009159" + ], + "absent epiphysis of the proximal phalanx of the 5th finger": [ + "HP:0009160" + ], + "absent end part of the innermost bone of little finger": [ + "HP:0009160" + ], + "absent end part of the innermost bone of pinkie finger": [ + "HP:0009160" + ], + "absent end part of the innermost bone of pinky finger": [ + "HP:0009160" + ], + "aplasia / hypoplasia of the middle phalanx of the 5th finger": [ + "HP:0009161" + ], + "absent / hypoplastic middle phalanx of 5th finger": [ + "HP:0009161" + ], + "absent / small middle bone of pinky finger": [ + "HP:0009161" + ], + "absent / underdevelop middle bone of little finger": [ + "HP:0009161" + ], + "absent / underdeveloped middle bone of little finger": [ + "HP:0009161" + ], + "absent / underdevelop middle bone of pinkie finger": [ + "HP:0009161" + ], + "absent / underdeveloped middle bone of pinkie finger": [ + "HP:0009161" + ], + "absent / underdevelop middle bone of pinky finger": [ + "HP:0009161" + ], + "absent / underdeveloped middle bone of pinky finger": [ + "HP:0009161" + ], + "absent middle phalanx of 5th finger": [ + "HP:0009162" + ], + "absent middle bone of little finger": [ + "HP:0009162" + ], + "absent middle bone of pinkie finger": [ + "HP:0009162" + ], + "absent middle bone of pinky finger": [ + "HP:0009162" + ], + "aplasia of the middle phalanx of the 5th finger": [ + "HP:0009162" + ], + "obsolete abnormal form of the 5th finger": [ + "HP:0009163" + ], + "abnormal calcification of the carpal bone": [ + "HP:0009164" + ], + "abnormal calcification of the carpal bones": [ + "HP:0009164" + ], + "abnormal calcification of the wrist bone": [ + "HP:0009164" + ], + "abnormal calcification of the wrist bones": [ + "HP:0009164" + ], + "carpal calcification": [ + "HP:0009164" + ], + "carpal calcifications": [ + "HP:0009164" + ], + "stippling of the epiphysis of the distal phalanx of the 5th finger": [ + "HP:0009165" + ], + "speckled calcification in end part of the outermost bone of little finger": [ + "HP:0009165" + ], + "speckled calcifications in end part of the outermost bone of little finger": [ + "HP:0009165" + ], + "speckled calcification in end part of the outermost bone of pinkie finger": [ + "HP:0009165" + ], + "speckled calcifications in end part of the outermost bone of pinkie finger": [ + "HP:0009165" + ], + "speckled calcification in end part of the outermost bone of pinky finger": [ + "HP:0009165" + ], + "speckled calcifications in end part of the outermost bone of pinky finger": [ + "HP:0009165" + ], + "fragmentation of the epiphysis of the distal phalanx of the 5th finger": [ + "HP:0009166" + ], + "fragmentation of end part of the outermost bone of little finger": [ + "HP:0009166" + ], + "fragmentation of end part of the outermost bone of pinkie finger": [ + "HP:0009166" + ], + "fragmentation of end part of the outermost bone of pinky finger": [ + "HP:0009166" + ], + "irregular epiphysis of the distal phalanx of the 5th finger": [ + "HP:0009167" + ], + "irregular end part of the outermost bone of little finger": [ + "HP:0009167" + ], + "irregular end part of the outermost bone of pinkie finger": [ + "HP:0009167" + ], + "irregular end part of the outermost bone of pinky finger": [ + "HP:0009167" + ], + "bullet - shape middle phalanx of the 5th finger": [ + "HP:0009168" + ], + "bullet - shaped middle phalanx of the 5th finger": [ + "HP:0009168" + ], + "bullet - shape middle little finger bone": [ + "HP:0009168" + ], + "bullet - shaped middle little finger bone": [ + "HP:0009168" + ], + "bullet - shape middle pinkie finger bone": [ + "HP:0009168" + ], + "bullet - shaped middle pinkie finger bone": [ + "HP:0009168" + ], + "bullet - shape middle pinky finger bone": [ + "HP:0009168" + ], + "bullet - shaped middle pinky finger bone": [ + "HP:0009168" + ], + "broad middle phalanx of the 5th finger": [ + "HP:0009169" + ], + "broad middle bone of little finger": [ + "HP:0009169" + ], + "broad middle bone of pinkie finger": [ + "HP:0009169" + ], + "broad middle bone of pinky finger": [ + "HP:0009169" + ], + "wide middle phalanx of the 5th finger": [ + "HP:0009169" + ], + "osteolytic defect of the middle phalanx of the 5th finger": [ + "HP:0009170" + ], + "osteolytic defects of the middle phalanx of the 5th finger": [ + "HP:0009170" + ], + "triangular epiphysis of the metacarpal": [ + "HP:0009171" + ], + "triangular epiphyses of the metacarpals": [ + "HP:0009171" + ], + "triangular end part of the long bone of hand": [ + "HP:0009171" + ], + "abnormal 4th finger phalanx morphology": [ + "HP:0009172" + ], + "abnormal bone of 4th finger": [ + "HP:0009172" + ], + "abnormal bones of 4th finger": [ + "HP:0009172" + ], + "abnormality of the phalanx of the ring finger": [ + "HP:0009172" + ], + "abnormality of the phalanges of the ring finger": [ + "HP:0009172" + ], + "curve middle phalanx of the 5th finger": [ + "HP:0009173" + ], + "curved middle phalanx of the 5th finger": [ + "HP:0009173" + ], + "curve middle bone of little finger": [ + "HP:0009173" + ], + "curved middle bone of little finger": [ + "HP:0009173" + ], + "curve middle bone of pinkie finger": [ + "HP:0009173" + ], + "curved middle bone of pinkie finger": [ + "HP:0009173" + ], + "curve middle bone of pinky finger": [ + "HP:0009173" + ], + "curved middle bone of pinky finger": [ + "HP:0009173" + ], + "abnormality of the epiphysis of the 4th finger": [ + "HP:0009174" + ], + "abnormality of the epiphyses of the 4th finger": [ + "HP:0009174" + ], + "abnormality of the end part of the ring finger": [ + "HP:0009174" + ], + "patchy sclerosis of the middle phalanx of the 5th finger": [ + "HP:0009175" + ], + "uneven increase in bone density in the middle bone of the little finger": [ + "HP:0009175" + ], + "uneven increase in bone density in the middle bone of the pinkie finger": [ + "HP:0009175" + ], + "uneven increase in bone density in the middle bone of the pinky finger": [ + "HP:0009175" + ], + "proximal / middle symphalangism of 5th finger": [ + "HP:0009177" + ], + "fuse innermost and middle bone of little finger": [ + "HP:0009177" + ], + "fused innermost and middle bones of little finger": [ + "HP:0009177" + ], + "fuse innermost and middle bone of pinkie finger": [ + "HP:0009177" + ], + "fused innermost and middle bones of pinkie finger": [ + "HP:0009177" + ], + "fuse innermost and middle bone of pinky finger": [ + "HP:0009177" + ], + "fused innermost and middle bones of pinky finger": [ + "HP:0009177" + ], + "proximal 5th finger symphalangism": [ + "HP:0009177" + ], + "proximal fifth finger symphalangism": [ + "HP:0009177" + ], + "symphalangism of the proximal and middle phalanx of the 5th finger": [ + "HP:0009177" + ], + "symphalangism of the proximal and middle phalanges of the 5th finger": [ + "HP:0009177" + ], + "symphalangism of middle phalanx of 5th finger": [ + "HP:0009178" + ], + "fuse middle bone of little finger": [ + "HP:0009178" + ], + "fused middle bones of little finger": [ + "HP:0009178" + ], + "fuse middle bone of pinkie finger": [ + "HP:0009178" + ], + "fused middle bones of pinkie finger": [ + "HP:0009178" + ], + "fuse middle bone of pinky finger": [ + "HP:0009178" + ], + "fused middle bones of pinky finger": [ + "HP:0009178" + ], + "deviation of the 5th finger": [ + "HP:0009179" + ], + "displace little finger": [ + "HP:0009179" + ], + "displaced little finger": [ + "HP:0009179" + ], + "displace pinkie finger": [ + "HP:0009179" + ], + "displaced pinkie finger": [ + "HP:0009179" + ], + "displace pinky finger": [ + "HP:0009179" + ], + "displaced pinky finger": [ + "HP:0009179" + ], + "laterally displace fifth finger": [ + "HP:0009179" + ], + "laterally displaced fifth finger": [ + "HP:0009179" + ], + "ulnar deviation of the 5th finger": [ + "HP:0009180" + ], + "triangular shape middle phalanx of the 5th finger": [ + "HP:0009182" + ], + "triangular shaped middle phalanx of the 5th finger": [ + "HP:0009182" + ], + "triangular shape middle little finger bone": [ + "HP:0009182" + ], + "triangular shaped middle little finger bone": [ + "HP:0009182" + ], + "triangular shape middle pinkie finger bone": [ + "HP:0009182" + ], + "triangular shaped middle pinkie finger bone": [ + "HP:0009182" + ], + "triangular shape middle pinky finger bone": [ + "HP:0009182" + ], + "triangular shaped middle pinky finger bone": [ + "HP:0009182" + ], + "joint contracture of the 5th finger": [ + "HP:0009183" + ], + "5th finger camptodactyly": [ + "HP:0009183" + ], + "fifth finger camptodactyly": [ + "HP:0009183" + ], + "contracture of the distal interphalangeal joint of the 5th finger": [ + "HP:0009184" + ], + "contracture of the proximal interphalangeal joint of the 5th finger": [ + "HP:0009185" + ], + "contracture of the metacarpophalangeal joint of the 5th finger": [ + "HP:0009186" + ], + "bracket epiphysis of the distal phalanx of the 5th finger": [ + "HP:0009187" + ], + "bracket shape end part of the outermost little finger bone": [ + "HP:0009187" + ], + "bracket shaped end part of the outermost little finger bone": [ + "HP:0009187" + ], + "bracket shape end part of the outermost pinkie finger bone": [ + "HP:0009187" + ], + "bracket shaped end part of the outermost pinkie finger bone": [ + "HP:0009187" + ], + "bracket shape end part of the outermost pinky finger bone": [ + "HP:0009187" + ], + "bracket shaped end part of the outermost pinky finger bone": [ + "HP:0009187" + ], + "pseudoepiphysis of the distal phalanx of the 5th finger": [ + "HP:0009188" + ], + "fragmentation of the metacarpal epiphysis": [ + "HP:0009189" + ], + "fragmentation of the metacarpal epiphyses": [ + "HP:0009189" + ], + "fragmentation of end part of the long bone of hand": [ + "HP:0009189" + ], + "irregular epiphysis of the metacarpal": [ + "HP:0009190" + ], + "irregular epiphyses of the metacarpals": [ + "HP:0009190" + ], + "irregular end part of the long bone of hand": [ + "HP:0009190" + ], + "ivory epiphysis of the metacarpal": [ + "HP:0009191" + ], + "ivory epiphyses of the metacarpals": [ + "HP:0009191" + ], + "increase bone density of end part of the long bone of hand": [ + "HP:0009191" + ], + "increased bone density of end part of the long bone of hands": [ + "HP:0009191" + ], + "aplasia / hypoplasia of the proximal phalanx of the 5th finger": [ + "HP:0009192" + ], + "absent / small innermost little finger bone": [ + "HP:0009192" + ], + "absent / small innermost pinkie finger bone": [ + "HP:0009192" + ], + "absent / small innermost pinky finger bone": [ + "HP:0009192" + ], + "absent / underdevelop innermost pinky finger bone": [ + "HP:0009192" + ], + "absent / underdeveloped innermost pinky finger bone": [ + "HP:0009192" + ], + "pseudoepiphyses of the metacarpal": [ + "HP:0009193" + ], + "pseudoepiphyses of the metacarpals": [ + "HP:0009193" + ], + "accessory proximal metacarpal ossification center": [ + "HP:0009193" + ], + "accessory proximal metacarpal ossification centers": [ + "HP:0009193" + ], + "accessory proximal metacarpal ossification centre": [ + "HP:0009193" + ], + "accessory proximal metacarpal ossification centres": [ + "HP:0009193" + ], + "metacarpal pseudoepiphyses": [ + "HP:0009193" + ], + "small epiphysis of the metacarpal": [ + "HP:0009194" + ], + "small epiphyses of the metacarpals": [ + "HP:0009194" + ], + "small end part of the long bone of hand": [ + "HP:0009194" + ], + "epiphyseal stippling of the metacarpal": [ + "HP:0009195" + ], + "epiphyseal stippling of the metacarpals": [ + "HP:0009195" + ], + "speckled calcification in end part of the long bone of hand": [ + "HP:0009195" + ], + "speckled calcifications in end part of the long bone of hand": [ + "HP:0009195" + ], + "stippling of the epiphysis of the metacarpal": [ + "HP:0009195" + ], + "stippling of the epiphyses of the metacarpals": [ + "HP:0009195" + ], + "absent metacarpal epiphysis": [ + "HP:0009196" + ], + "absent metacarpal epiphyses": [ + "HP:0009196" + ], + "absent end part of the long bone of hand": [ + "HP:0009196" + ], + "absent metacarpal ossification center": [ + "HP:0009196" + ], + "absent metacarpal ossification centre": [ + "HP:0009196" + ], + "bracket epiphysis of the proximal phalanx of the 5th finger": [ + "HP:0009197" + ], + "bracket shape end part of the innermost bone of the little finger": [ + "HP:0009197" + ], + "bracket shaped end part of the innermost bone of the little finger": [ + "HP:0009197" + ], + "bracket shape end part of the innermost bone of the pinkie finger": [ + "HP:0009197" + ], + "bracket shaped end part of the innermost bone of the pinkie finger": [ + "HP:0009197" + ], + "bracket shape end part of the innermost bone of the pinky finger": [ + "HP:0009197" + ], + "bracket shaped end part of the innermost bone of the pinky finger": [ + "HP:0009197" + ], + "abnormality of the epiphysis of the distal phalanx of the 5th finger": [ + "HP:0009198" + ], + "abnormality of end part of the outermost bone of the little finger": [ + "HP:0009198" + ], + "abnormality of end part of the outermost bone of the pinkie finger": [ + "HP:0009198" + ], + "abnormality of end part of the outermost bone of the pinky finger": [ + "HP:0009198" + ], + "abnormality of the epiphysis of the terminal phalanx of the little finger": [ + "HP:0009198" + ], + "irregular epiphysis of the proximal phalanx of the 5th finger": [ + "HP:0009199" + ], + "irregular end part of the innermost little finger bone": [ + "HP:0009199" + ], + "irregular end part of the innermost pinkie finger bone": [ + "HP:0009199" + ], + "irregular end part of the innermost pinky finger bone": [ + "HP:0009199" + ], + "pseudoepiphysis of the proximal phalanx of the 5th finger": [ + "HP:0009200" + ], + "stippling of the epiphysis of the proximal phalanx of the 5th finger": [ + "HP:0009201" + ], + "speckled calcification in end part of the innnermost bone of the little finger": [ + "HP:0009201" + ], + "speckled calcifications in end part of the innnermost bone of the little finger": [ + "HP:0009201" + ], + "speckled calcification in end part of the innnermost bone of the pinkie finger": [ + "HP:0009201" + ], + "speckled calcifications in end part of the innnermost bone of the pinkie finger": [ + "HP:0009201" + ], + "speckled calcification in end part of the innnermost bone of the pinky finger": [ + "HP:0009201" + ], + "speckled calcifications in end part of the innnermost bone of the pinky finger": [ + "HP:0009201" + ], + "fragmentation of the epiphysis of the proximal phalanx of the 5th finger": [ + "HP:0009202" + ], + "fragmentation of end part of the innermost bone of the little finger": [ + "HP:0009202" + ], + "fragmentation of end part of the innermost bone of the pinkie finger": [ + "HP:0009202" + ], + "fragmentation of end part of the innermost bone of the pinky finger": [ + "HP:0009202" + ], + "absent epiphysis of the middle phalanx of the 5th finger": [ + "HP:0009203" + ], + "absent end part of the middle bone of the little finger": [ + "HP:0009203" + ], + "absent end part of the middle bone of the pinkie finger": [ + "HP:0009203" + ], + "absent end part of the middle bone of the pinky finger": [ + "HP:0009203" + ], + "bracket epiphysis of the middle phalanx of the 5th finger": [ + "HP:0009204" + ], + "bracket shape end part of the middle bone of the little finger": [ + "HP:0009204" + ], + "bracket shaped end part of the middle bone of the little finger": [ + "HP:0009204" + ], + "bracket shape end part of the middle bone of the pinkie finger": [ + "HP:0009204" + ], + "bracket shaped end part of the middle bone of the pinkie finger": [ + "HP:0009204" + ], + "bracket shape end part of the middle bone of the pinky finger": [ + "HP:0009204" + ], + "bracket shaped end part of the middle bone of the pinky finger": [ + "HP:0009204" + ], + "cone - shaped epiphysis of the middle phalanx of the 5th finger": [ + "HP:0009205" + ], + "cone - shaped end part of the middle bone of the little finger": [ + "HP:0009205" + ], + "cone - shaped end part of the middle bone of the pinkie finger": [ + "HP:0009205" + ], + "cone - shaped end part of the middle bone of the pinky finger": [ + "HP:0009205" + ], + "enlarged epiphysis of the middle phalanx of the 5th finger": [ + "HP:0009206" + ], + "enlarged end part of the middle bone of the little finger": [ + "HP:0009206" + ], + "enlarged end part of the middle bone of the pinkie finger": [ + "HP:0009206" + ], + "enlarged end part of the middle bone of the pinky finger": [ + "HP:0009206" + ], + "fragmentation of the epiphysis of the middle phalanx of the 5th finger": [ + "HP:0009207" + ], + "fragmentation of end part of the middle bone of the little finger": [ + "HP:0009207" + ], + "fragmentation of end part of the middle bone of the pinkie finger": [ + "HP:0009207" + ], + "fragmentation of end part of the middle bone of the pinky finger": [ + "HP:0009207" + ], + "irregular epiphysis of the middle phalanx of the 5th finger": [ + "HP:0009208" + ], + "irregular end part of the middle bone of the little finger": [ + "HP:0009208" + ], + "irregular end part of the middle bone of the pinkie finger": [ + "HP:0009208" + ], + "irregular end part of the middle bone of the pinky finger": [ + "HP:0009208" + ], + "ivory epiphysis of the middle phalanx of the 5th finger": [ + "HP:0009209" + ], + "increase bone density of end part of the middle bone of little finger": [ + "HP:0009209" + ], + "increased bone density of end part of the middle bone of little finger": [ + "HP:0009209" + ], + "increase bone density of end part of the middle bone of pinkie finger": [ + "HP:0009209" + ], + "increased bone density of end part of the middle bone of pinkie finger": [ + "HP:0009209" + ], + "increase bone density of end part of the middle bone of pinky finger": [ + "HP:0009209" + ], + "increased bone density of end part of the middle bone of pinky finger": [ + "HP:0009209" + ], + "pseudoepiphysis of the middle phalanx of the 5th finger": [ + "HP:0009210" + ], + "small epiphysis of the middle phalanx of the 5th finger": [ + "HP:0009211" + ], + "small end part of the middle bone of the little finger": [ + "HP:0009211" + ], + "small end part of the middle bone of the pinkie finger": [ + "HP:0009211" + ], + "small end part of the middle bone of the pinky finger": [ + "HP:0009211" + ], + "stippling of the epiphysis of the middle phalanx of the 5th finger": [ + "HP:0009212" + ], + "speckled calcification in end part of the middle bone of the little finger": [ + "HP:0009212" + ], + "speckled calcifications in end part of the middle bone of the little finger": [ + "HP:0009212" + ], + "speckled calcification in end part of the middle bone of the pinkie finger": [ + "HP:0009212" + ], + "speckled calcifications in end part of the middle bone of the pinkie finger": [ + "HP:0009212" + ], + "speckled calcification in end part of the middle bone of the pinky finger": [ + "HP:0009212" + ], + "speckled calcifications in end part of the middle bone of the pinky finger": [ + "HP:0009212" + ], + "triangular epiphysis of the middle phalanx of the 5th finger": [ + "HP:0009213" + ], + "delta - shaped epiphysis of the middle phalanx of the 5th finger": [ + "HP:0009213" + ], + "triangular end part of the middle bone of the little finger": [ + "HP:0009213" + ], + "triangular end part of the middle bone of the pinkie finger": [ + "HP:0009213" + ], + "triangular end part of the middle bone of the pinky finger": [ + "HP:0009213" + ], + "absent epiphysis of the middle phalanx of the 4th finger": [ + "HP:0009214" + ], + "absent end part of the middle bone of the ring finger": [ + "HP:0009214" + ], + "bracket epiphysis of the middle phalanx of the 4th finger": [ + "HP:0009215" + ], + "bracket shape end part of the middle bone of the ring finger": [ + "HP:0009215" + ], + "bracket shaped end part of the middle bone of the ring finger": [ + "HP:0009215" + ], + "cone - shaped epiphysis of the middle phalanx of the 4th finger": [ + "HP:0009216" + ], + "cone - shaped end part of the middle bone of the ring finger": [ + "HP:0009216" + ], + "enlarged epiphysis of the middle phalanx of the 4th finger": [ + "HP:0009217" + ], + "enlarged end part of the middle bone of the ring finger": [ + "HP:0009217" + ], + "fragmentation of the epiphysis of the middle phalanx of the 4th finger": [ + "HP:0009218" + ], + "fragmentation of end part of the middle bone of the ring finger": [ + "HP:0009218" + ], + "irregular epiphysis of the middle phalanx of the 4th finger": [ + "HP:0009219" + ], + "irregular end part of the middle bone of the ring finger": [ + "HP:0009219" + ], + "ivory epiphysis of the middle phalanx of the 4th finger": [ + "HP:0009220" + ], + "increase bone density of end part of the middle ring finger bone": [ + "HP:0009220" + ], + "increased bone density of end part of the middle ring finger bone": [ + "HP:0009220" + ], + "pseudoepiphysis of the middle phalanx of the 4th finger": [ + "HP:0009221" + ], + "small epiphysis of the middle phalanx of the 4th finger": [ + "HP:0009222" + ], + "small end part of the middle bone of the ring finger": [ + "HP:0009222" + ], + "stippling of the epiphysis of the middle phalanx of the 4th finger": [ + "HP:0009223" + ], + "speckled calcification in end part of the middle bone of the ring finger": [ + "HP:0009223" + ], + "speckled calcifications in end part of the middle bone of the ring finger": [ + "HP:0009223" + ], + "triangular epiphysis of the middle phalanx of the 4th finger": [ + "HP:0009224" + ], + "delta - shaped epiphysis of the middle phalanx of the 4th finger": [ + "HP:0009224" + ], + "triangular end part of the middle bone of the ring finger": [ + "HP:0009224" + ], + "aplasia of the proximal phalanx of the 5th finger": [ + "HP:0009225" + ], + "absent innermost bone of little finger": [ + "HP:0009225" + ], + "absent innermost bone of pinkie finger": [ + "HP:0009225" + ], + "absent innermost bone of pinky finger": [ + "HP:0009225" + ], + "short proximal phalanx of the 5th finger": [ + "HP:0009226" + ], + "hypoplastic / small proximal phalanx of the 5th finger": [ + "HP:0009226" + ], + "short innermost little finger bone": [ + "HP:0009226" + ], + "short innermost pinkie finger bone": [ + "HP:0009226" + ], + "short innermost pinky finger bone": [ + "HP:0009226" + ], + "short proximal phalanx of the fifth finger": [ + "HP:0009226" + ], + "broad proximal phalanx of the 5th finger": [ + "HP:0009227" + ], + "broad innermost little finger bone": [ + "HP:0009227" + ], + "broad innermost pinkie finger bone": [ + "HP:0009227" + ], + "broad innermost pinky finger bone": [ + "HP:0009227" + ], + "wide proximal phalanx of the 5th finger": [ + "HP:0009227" + ], + "bullet - shape proximal phalanx of the 5th finger": [ + "HP:0009228" + ], + "bullet - shaped proximal phalanx of the 5th finger": [ + "HP:0009228" + ], + "bullet - shape innermost little finger bone": [ + "HP:0009228" + ], + "bullet - shaped innermost little finger bone": [ + "HP:0009228" + ], + "bullet - shape innermost pinkie finger bone": [ + "HP:0009228" + ], + "bullet - shaped innermost pinkie finger bone": [ + "HP:0009228" + ], + "bullet - shape innermost pinky finger bone": [ + "HP:0009228" + ], + "bullet - shaped innermost pinky finger bone": [ + "HP:0009228" + ], + "curve proximal phalanx of the 5th finger": [ + "HP:0009229" + ], + "curved proximal phalanx of the 5th finger": [ + "HP:0009229" + ], + "curve innermost bone of little finger": [ + "HP:0009229" + ], + "curved innermost bone of little finger": [ + "HP:0009229" + ], + "curve innermost bone of pinkie finger": [ + "HP:0009229" + ], + "curved innermost bone of pinkie finger": [ + "HP:0009229" + ], + "curve innermost bone of pinky finger": [ + "HP:0009229" + ], + "curved innermost bone of pinky finger": [ + "HP:0009229" + ], + "osteolytic defect of the proximal phalanx of the 5th finger": [ + "HP:0009230" + ], + "osteolytic defects of the proximal phalanx of the 5th finger": [ + "HP:0009230" + ], + "patchy sclerosis of the proximal phalanx of the 5th finger": [ + "HP:0009231" + ], + "uneven increase in bone density in the innermost bone of little finger": [ + "HP:0009231" + ], + "uneven increase in bone density in the innermost bone of pinkie finger": [ + "HP:0009231" + ], + "uneven increase in bone density in the innermost bone of pinky finger": [ + "HP:0009231" + ], + "symphalangism affect the proximal phalanx of the 5th finger": [ + "HP:0009232" + ], + "symphalangism affecting the proximal phalanx of the 5th finger": [ + "HP:0009232" + ], + "fuse innermost bone of little finger": [ + "HP:0009232" + ], + "fused innermost bone of little finger": [ + "HP:0009232" + ], + "fuse innermost bone of pinkie finger": [ + "HP:0009232" + ], + "fused innermost bone of pinkie finger": [ + "HP:0009232" + ], + "fuse innermost bone of pinky finger": [ + "HP:0009232" + ], + "fused innermost bone of pinky finger": [ + "HP:0009232" + ], + "triangular shape proximal phalanx of the 5th finger": [ + "HP:0009233" + ], + "triangular shaped proximal phalanx of the 5th finger": [ + "HP:0009233" + ], + "triangular shape innermost little finger bone": [ + "HP:0009233" + ], + "triangular shaped innermost little finger bone": [ + "HP:0009233" + ], + "triangular shape innermost pinkie finger bone": [ + "HP:0009233" + ], + "triangular shaped innermost pinkie finger bone": [ + "HP:0009233" + ], + "triangular shape innermost pinky finger bone": [ + "HP:0009233" + ], + "triangular shaped innermost pinky finger bone": [ + "HP:0009233" + ], + "symphalangism of the proximal phalanx of the 5th finger with the 5th metacarpal": [ + "HP:0009234" + ], + "fuse innermost bone of little finger with 5th long bone of hand": [ + "HP:0009234" + ], + "fused innermost bone of little finger with 5th long bone of hand": [ + "HP:0009234" + ], + "fuse innermost bone of pinkie finger with 5th long bone of hand": [ + "HP:0009234" + ], + "fused innermost bone of pinkie finger with 5th long bone of hand": [ + "HP:0009234" + ], + "fuse innermost bone of pinky finger with 5th long bone of hand": [ + "HP:0009234" + ], + "fused innermost bone of pinky finger with 5th long bone of hand": [ + "HP:0009234" + ], + "rhomboid or triangular shape 5th finger proximal phalanx": [ + "HP:0009236" + ], + "rhomboid or triangular shaped 5th finger proximal phalanx": [ + "HP:0009236" + ], + "rhomboid or triangular shape innermost bone of little finger": [ + "HP:0009236" + ], + "rhomboid or triangular shaped innermost bone of little finger": [ + "HP:0009236" + ], + "rhomboid or triangular shape innermost bone of pinkie finger": [ + "HP:0009236" + ], + "rhomboid or triangular shaped innermost bone of pinkie finger": [ + "HP:0009236" + ], + "rhomboid or triangular shape innermost bone of pinky finger": [ + "HP:0009236" + ], + "rhomboid or triangular shaped innermost bone of pinky finger": [ + "HP:0009236" + ], + "short 5th finger": [ + "HP:0009237" + ], + "fifth finger brachydactyly": [ + "HP:0009237" + ], + "hypoplastic phalanx of the little finger": [ + "HP:0009237" + ], + "hypoplastic phalanges of the little finger": [ + "HP:0009237" + ], + "hypoplastic / small 5th finger": [ + "HP:0009237" + ], + "hypoplastic / small little finger": [ + "HP:0009237" + ], + "short fifth finger": [ + "HP:0009237" + ], + "short fifth fingers": [ + "HP:0009237" + ], + "short little finger": [ + "HP:0009237" + ], + "short phalanx of the little finger": [ + "HP:0009237" + ], + "short phalanges of the little finger": [ + "HP:0009237" + ], + "short pinkie finger": [ + "HP:0009237" + ], + "short pinky finger": [ + "HP:0009237" + ], + "aplasia of the 5th finger": [ + "HP:0009238" + ], + "absent little finger": [ + "HP:0009238" + ], + "absent pinkie finger": [ + "HP:0009238" + ], + "absent pinky finger": [ + "HP:0009238" + ], + "aplasia / hypoplasia of the distal phalanx of the 5th finger": [ + "HP:0009239" + ], + "absent / small outermost bone of little finger": [ + "HP:0009239" + ], + "absent / small outermost bone of pinkie finger": [ + "HP:0009239" + ], + "absent / small outermost bone of pinky finger": [ + "HP:0009239" + ], + "absent / underdevelop outermost bone of pinky finger": [ + "HP:0009239" + ], + "absent / underdeveloped outermost bone of pinky finger": [ + "HP:0009239" + ], + "broad distal phalanx of the 5th finger": [ + "HP:0009240" + ], + "broad outermost little finger bone": [ + "HP:0009240" + ], + "broad outermost pinkie finger bone": [ + "HP:0009240" + ], + "broad outermost pinky finger bone": [ + "HP:0009240" + ], + "wide outermost pinky finger bone": [ + "HP:0009240" + ], + "bullet - shaped distal phalanx of the 5th finger": [ + "HP:0009241" + ], + "bullet - shape outermost little finger bone": [ + "HP:0009241" + ], + "bullet - shaped outermost little finger bone": [ + "HP:0009241" + ], + "bullet - shape outermost pinkie finger bone": [ + "HP:0009241" + ], + "bullet - shaped outermost pinkie finger bone": [ + "HP:0009241" + ], + "bullet - shape outermost pinky finger bone": [ + "HP:0009241" + ], + "bullet - shaped outermost pinky finger bone": [ + "HP:0009241" + ], + "osteolytic defect of the distal phalanx of the 5th finger": [ + "HP:0009242" + ], + "osteolytic defects of the distal phalanx of the 5th finger": [ + "HP:0009242" + ], + "patchy sclerosis of the distal phalanx of the 5th finger": [ + "HP:0009243" + ], + "uneven increase in bone density in the outermost bone of little finger": [ + "HP:0009243" + ], + "uneven increase in bone density in the outermost bone of pinkie finger": [ + "HP:0009243" + ], + "uneven increase in bone density in the outermost bone of pinky finger": [ + "HP:0009243" + ], + "distal / middle symphalangism of 5th finger": [ + "HP:0009244" + ], + "fifth finger distal interphalangeal joint symphalangism": [ + "HP:0009244" + ], + "fused end and middle bone of little finger": [ + "HP:0009244" + ], + "fused end and middle bones of little finger": [ + "HP:0009244" + ], + "fused end and middle bone of pinkie finger": [ + "HP:0009244" + ], + "fused end and middle bones of pinkie finger": [ + "HP:0009244" + ], + "fused end and middle bone of pinky finger": [ + "HP:0009244" + ], + "fused end and middle bones of pinky finger": [ + "HP:0009244" + ], + "fusion of the terminal and middle phalanx of the 5th finger": [ + "HP:0009244" + ], + "fusion of the terminal and middle phalanges of the 5th finger": [ + "HP:0009244" + ], + "symphalangism of the distal and middle phalanx of the 5th finger": [ + "HP:0009244" + ], + "symphalangism of the distal and middle phalanges of the 5th finger": [ + "HP:0009244" + ], + "symphalangism of the terminal and middle phalanx of the 5th finger": [ + "HP:0009244" + ], + "symphalangism of the terminal and middle phalanges of the 5th finger": [ + "HP:0009244" + ], + "triangular shape distal phalanx of the 5th finger": [ + "HP:0009245" + ], + "triangular shaped distal phalanx of the 5th finger": [ + "HP:0009245" + ], + "triangular shape outermost little finger bone": [ + "HP:0009245" + ], + "triangular shaped outermost little finger bone": [ + "HP:0009245" + ], + "triangular shape outermost pinkie finger bone": [ + "HP:0009245" + ], + "triangular shaped outermost pinkie finger bone": [ + "HP:0009245" + ], + "triangular shape outermost pinky finger bone": [ + "HP:0009245" + ], + "triangular shaped outermost pinky finger bone": [ + "HP:0009245" + ], + "aplasia of the distal phalanx of the 5th finger": [ + "HP:0009246" + ], + "absent outermost little finger bone": [ + "HP:0009246" + ], + "absent outermost pinkie finger bone": [ + "HP:0009246" + ], + "absent outermost pinky finger bone": [ + "HP:0009246" + ], + "abnormality of the epiphysis of the middle phalanx of the 4th finger": [ + "HP:0009247" + ], + "abnormality of the end part of the middle bone of the ring finger": [ + "HP:0009247" + ], + "abnormality of the epiphysis of the proximal phalanx of the 4th finger": [ + "HP:0009248" + ], + "abnormality of the end part of the innermost bone of the ring finger": [ + "HP:0009248" + ], + "abnormality of the epiphysis of the distal phalanx of the 4th finger": [ + "HP:0009249" + ], + "abnormality of the end part of the outermost bone of the ring finger": [ + "HP:0009249" + ], + "absent epiphysis of the distal phalanx of the 4th finger": [ + "HP:0009250" + ], + "absent end part of the outermost bone of the ring finger": [ + "HP:0009250" + ], + "bracket epiphysis of the distal phalanx of the 4th finger": [ + "HP:0009251" + ], + "bracket shape end part of the outermost bone of the ring finger": [ + "HP:0009251" + ], + "bracket shaped end part of the outermost bone of the ring finger": [ + "HP:0009251" + ], + "cone - shaped epiphysis of the distal phalanx of the 4th finger": [ + "HP:0009252" + ], + "cone - shaped end part of the outermost bone of the ring finger": [ + "HP:0009252" + ], + "enlarged epiphysis of the distal phalanx of the 4th finger": [ + "HP:0009253" + ], + "enlarged end part of the outermost bone of the ring finger": [ + "HP:0009253" + ], + "fragmentation of the epiphysis of the distal phalanx of the 4th finger": [ + "HP:0009254" + ], + "fragmentation of end part of the outermost bone of the ring finger": [ + "HP:0009254" + ], + "irregular epiphysis of the distal phalanx of the 4th finger": [ + "HP:0009255" + ], + "irregular end part of the outermost bone of the ring finger": [ + "HP:0009255" + ], + "ivory epiphysis of the distal phalanx of the 4th finger": [ + "HP:0009256" + ], + "increase bone density of end part of the outermost ring finger bone": [ + "HP:0009256" + ], + "increased bone density of end part of the outermost ring finger bone": [ + "HP:0009256" + ], + "pseudoepiphysis of the distal phalanx of the 4th finger": [ + "HP:0009257" + ], + "small epiphysis of the distal phalanx of the 4th finger": [ + "HP:0009258" + ], + "small end part of the outermost bone of the ring finger": [ + "HP:0009258" + ], + "stippling of the epiphysis of the distal phalanx of the 4th finger": [ + "HP:0009259" + ], + "speckled calcification in the end part of the outermost bone of the ring finger": [ + "HP:0009259" + ], + "speckled calcifications in the end part of the outermost bone of the ring finger": [ + "HP:0009259" + ], + "triangular epiphysis of the distal phalanx of the 4th finger": [ + "HP:0009260" + ], + "delta - shaped epiphysis of the distal phalanx of the 4th finger": [ + "HP:0009260" + ], + "triangular end part of the outermost bone of ring finger": [ + "HP:0009260" + ], + "absent epiphysis of the proximal phalanx of the 4th finger": [ + "HP:0009261" + ], + "absent end part of the innermost bone of the ring finger": [ + "HP:0009261" + ], + "bracket epiphysis of the proximal phalanx of the 4th finger": [ + "HP:0009262" + ], + "bracket proximal epiphysis of the ring finger": [ + "HP:0009262" + ], + "bracket shape end part of the innermost bone of the ring finger": [ + "HP:0009262" + ], + "bracket shaped end part of the innermost bone of the ring finger": [ + "HP:0009262" + ], + "cone - shaped epiphysis of the proximal phalanx of the 4th finger": [ + "HP:0009263" + ], + "cone - shaped end part of the innermost bone of the ring finger": [ + "HP:0009263" + ], + "enlarged epiphysis of the proximal phalanx of the 4th finger": [ + "HP:0009264" + ], + "enlarged end part of the innermost bone of the ring finger": [ + "HP:0009264" + ], + "fragmentation of the epiphysis of the proximal phalanx of the 4th finger": [ + "HP:0009265" + ], + "fragmentation of end part of the innermost bone of the ring finger": [ + "HP:0009265" + ], + "irregular epiphysis of the proximal phalanx of the 4th finger": [ + "HP:0009266" + ], + "irregular end part of the innermost bone of the ring finger": [ + "HP:0009266" + ], + "ivory epiphysis of the proximal phalanx of the 4th finger": [ + "HP:0009267" + ], + "increase bone density of end part of the innermost ring finger bone": [ + "HP:0009267" + ], + "increased bone density of end part of the innermost ring finger bone": [ + "HP:0009267" + ], + "pseudoepiphysis of the proximal phalanx of the 4th finger": [ + "HP:0009268" + ], + "small epiphysis of the proximal phalanx of the 4th finger": [ + "HP:0009269" + ], + "small end part of the innermost bone of the ring finger": [ + "HP:0009269" + ], + "stippling of the epiphysis of the proximal phalanx of the 4th finger": [ + "HP:0009270" + ], + "speckled calcification in end part of the innermost bone of ring finger": [ + "HP:0009270" + ], + "speckled calcifications in end part of the innermost bone of ring finger": [ + "HP:0009270" + ], + "triangular epiphysis of the proximal phalanx of the 4th finger": [ + "HP:0009271" + ], + "delta - shaped epiphysis of the proximal phalanx of the 4th finger": [ + "HP:0009271" + ], + "triangular end part of the innermost bone of ring finger": [ + "HP:0009271" + ], + "aplasia / hypoplasia of the 4th finger": [ + "HP:0009272" + ], + "absent / small ring finger bone": [ + "HP:0009272", + "HP:0009408" + ], + "absent / underdevelop ring finger bone": [ + "HP:0009272", + "HP:0009408" + ], + "absent / underdeveloped ring finger bone": [ + "HP:0009272" + ], + "deviation of the 4th finger": [ + "HP:0009273" + ], + "deviation of the ring finger": [ + "HP:0009273" + ], + "joint contracture of the 4th finger": [ + "HP:0009274" + ], + "joint contracture of the fourth finger": [ + "HP:0009274" + ], + "joint contractures of the fourth finger": [ + "HP:0009274" + ], + "contracture of the distal interphalangeal joint of the 4th finger": [ + "HP:0009275" + ], + "contracture of the proximal interphalangeal joint of the 4th finger": [ + "HP:0009276" + ], + "4th finger camptodactyly": [ + "HP:0009276" + ], + "camptodactyly of the 4th finger": [ + "HP:0009276" + ], + "camptodactyly of the ring finger": [ + "HP:0009276" + ], + "contracture of the metacarpophalangeal joint of the 4th finger": [ + "HP:0009277" + ], + "ulnar deviation of the 4th finger": [ + "HP:0009278" + ], + "ulnar deviation of the ring finger": [ + "HP:0009278" + ], + "radial deviation of the 4th finger": [ + "HP:0009279" + ], + "radial deviation of the ring finger": [ + "HP:0009279" + ], + "short 4th finger": [ + "HP:0009280" + ], + "hypoplastic / small 4th finger": [ + "HP:0009280" + ], + "short ring finger": [ + "HP:0009280" + ], + "aplasia of the 4th finger": [ + "HP:0009281" + ], + "absent ring finger": [ + "HP:0009281" + ], + "abnormality of the distal phalanx of the 4th finger": [ + "HP:0009282" + ], + "abnormality of the outermost bone of ring finger": [ + "HP:0009282" + ], + "abnormality of the middle phalanx of the 4th finger": [ + "HP:0009283" + ], + "abnormal middle bone of ring finger": [ + "HP:0009283" + ], + "abnormality of the middle phalanx of the ring finger": [ + "HP:0009283" + ], + "abnormality of the proximal phalanx of the 4th finger": [ + "HP:0009284" + ], + "abnormal innermost bone of ring finger": [ + "HP:0009284" + ], + "abnormality of the proximal phalanx of the ring finger": [ + "HP:0009284" + ], + "curve phalanx of the 4th finger": [ + "HP:0009285" + ], + "curved phalanges of the 4th finger": [ + "HP:0009285" + ], + "curve ring finger bone": [ + "HP:0009285" + ], + "curved ring finger bone": [ + "HP:0009285" + ], + "curve distal phalanx of the 4th finger": [ + "HP:0009286" + ], + "curved distal phalanx of the 4th finger": [ + "HP:0009286" + ], + "curve outermost ring finger bone": [ + "HP:0009286" + ], + "curved outermost ring finger bone": [ + "HP:0009286" + ], + "curve middle phalanx of the 4th finger": [ + "HP:0009287" + ], + "curved middle phalanx of the 4th finger": [ + "HP:0009287" + ], + "curve middle ring finger bone": [ + "HP:0009287" + ], + "curved middle ring finger bone": [ + "HP:0009287" + ], + "curve proximal phalanx of the 4th finger": [ + "HP:0009288" + ], + "curved proximal phalanx of the 4th finger": [ + "HP:0009288" + ], + "curve innermost ring finger bone": [ + "HP:0009288" + ], + "curved innermost ring finger bone": [ + "HP:0009288" + ], + "aplasia / hypoplasia of the distal phalanx of the 4th finger": [ + "HP:0009289" + ], + "absent / small outermost ring finger bone": [ + "HP:0009289" + ], + "absent / underdevelop outermost ring finger bone": [ + "HP:0009289" + ], + "absent / underdeveloped outermost ring finger bone": [ + "HP:0009289" + ], + "short distal phalanx of the 4th finger": [ + "HP:0009290" + ], + "hypoplastic / small distal phalanx of the 4th finger": [ + "HP:0009290" + ], + "short distal phalanx of the fourth finger": [ + "HP:0009290" + ], + "short outermost bone of ring finger": [ + "HP:0009290" + ], + "aplasia of the distal phalanx of the 4th finger": [ + "HP:0009291" + ], + "absent outermost bone of ring finger": [ + "HP:0009291" + ], + "broad distal phalanx of the 4th finger": [ + "HP:0009292" + ], + "broad outermost bone of ring finger": [ + "HP:0009292" + ], + "wide outermost bone of ring finger": [ + "HP:0009292" + ], + "broad middle phalanx of the 4th finger": [ + "HP:0009293" + ], + "broad middle bone of the 4th finger": [ + "HP:0009293" + ], + "absent middle phalanx of 4th finger": [ + "HP:0009294" + ], + "absent middle bone of 4th finger": [ + "HP:0009294" + ], + "aplasia of the middle phalanx of the 4th finger": [ + "HP:0009294" + ], + "short middle phalanx of the 4th finger": [ + "HP:0009295" + ], + "brachymesophalangy iv ( finger )": [ + "HP:0009295" + ], + "hypoplastic / small middle phalanx of ring finger": [ + "HP:0009295" + ], + "hypoplastic / small middle phalanx of the 4th finger": [ + "HP:0009295" + ], + "short middle bone of 4th finger": [ + "HP:0009295" + ], + "short middle phalanx of ring finger": [ + "HP:0009295" + ], + "bullet - shape middle phalanx of the 4th finger": [ + "HP:0009296" + ], + "bullet - shaped middle phalanx of the 4th finger": [ + "HP:0009296" + ], + "bullet - shape middle bone of the 4th finger": [ + "HP:0009296" + ], + "bullet - shaped middle bone of the 4th finger": [ + "HP:0009296" + ], + "osteolytic defect of the middle phalanx of the 4th finger": [ + "HP:0009297" + ], + "osteolytic defects of the middle phalanx of the 4th finger": [ + "HP:0009297" + ], + "aplasia of the proximal phalanx of the 4th finger": [ + "HP:0009298" + ], + "absent innermost ring finger bone": [ + "HP:0009298" + ], + "aplasia / hypoplasia of the middle phalanx of the 4th finger": [ + "HP:0009299" + ], + "absent / small middle ring finger bone": [ + "HP:0009299" + ], + "absent / underdevelop middle ring finger bone": [ + "HP:0009299" + ], + "absent / underdeveloped middle ring finger bone": [ + "HP:0009299" + ], + "aplasia / hypoplasia of the proximal phalanx of the 4th finger": [ + "HP:0009300" + ], + "absent / small innermost ring finger bone": [ + "HP:0009300" + ], + "absent / underdevelop innermost ring finger bone": [ + "HP:0009300" + ], + "absent / underdeveloped innermost ring finger bone": [ + "HP:0009300" + ], + "short proximal phalanx of the 4th finger": [ + "HP:0009301" + ], + "hypoplastic / small proximal phalanx of the 4th finger": [ + "HP:0009301" + ], + "short innermost bone of the ring finger": [ + "HP:0009301" + ], + "short proximal phalanx of the fourth finger": [ + "HP:0009301" + ], + "bullet - shaped distal phalanx of the 4th finger": [ + "HP:0009302" + ], + "bullet - shape outermost bone of ring finger": [ + "HP:0009302" + ], + "bullet - shaped outermost bone of ring finger": [ + "HP:0009302" + ], + "osteolytic defect of the distal phalanx of the 4th finger": [ + "HP:0009303" + ], + "osteolytic defects of the distal phalanx of the 4th finger": [ + "HP:0009303" + ], + "patchy sclerosis of the distal phalanx of the 4th finger": [ + "HP:0009304" + ], + "uneven increase in bone density in the outermost bone of the ring finger": [ + "HP:0009304" + ], + "distal / middle symphalangism of 4th finger": [ + "HP:0009305" + ], + "fuse outermost and middle bone of ring finger": [ + "HP:0009305" + ], + "fused outermost and middle bones of ring finger": [ + "HP:0009305" + ], + "symphalangism of the distal and middle phalanx of the 4th finger": [ + "HP:0009305" + ], + "symphalangism of the distal and middle phalanges of the 4th finger": [ + "HP:0009305" + ], + "triangular shape distal phalanx of the 4th finger": [ + "HP:0009306" + ], + "triangular shaped distal phalanx of the 4th finger": [ + "HP:0009306" + ], + "triangular shape outermost bone of the ring finger": [ + "HP:0009306" + ], + "triangular shaped outermost bone of the ring finger": [ + "HP:0009306" + ], + "patchy sclerosis of the middle phalanx of the 4th finger": [ + "HP:0009307" + ], + "uneven increase in bone density in the middle bone of the ring finger": [ + "HP:0009307" + ], + "symphalangism of middle phalanx of 4th finger": [ + "HP:0009308" + ], + "fuse middle bone of ring finger": [ + "HP:0009308" + ], + "fused middle bone of ring finger": [ + "HP:0009308" + ], + "triangular shape middle phalanx of the 4th finger": [ + "HP:0009309" + ], + "triangular shaped middle phalanx of the 4th finger": [ + "HP:0009309" + ], + "triangular shape middle bone of the ring finger": [ + "HP:0009309" + ], + "triangular shaped middle bone of the ring finger": [ + "HP:0009309" + ], + "broad proximal phalanx of the 4th finger": [ + "HP:0009310" + ], + "broad innermost ring finger bone": [ + "HP:0009310" + ], + "bullet - shape proximal phalanx of the 4th finger": [ + "HP:0009311" + ], + "bullet - shaped proximal phalanx of the 4th finger": [ + "HP:0009311" + ], + "bullet - shape innermost ring finger bone": [ + "HP:0009311" + ], + "bullet - shaped innermost ring finger bone": [ + "HP:0009311" + ], + "osteolytic defect of the proximal phalanx of the 4th finger": [ + "HP:0009312" + ], + "osteolytic defects of the proximal phalanx of the 4th finger": [ + "HP:0009312" + ], + "patchy sclerosis of the proximal phalanx of the 4th finger": [ + "HP:0009313" + ], + "uneven increase in bone density in the innermost bone of the ring finger": [ + "HP:0009313" + ], + "symphalangism affect the proximal phalanx of the 4th finger": [ + "HP:0009314" + ], + "symphalangism affecting the proximal phalanx of the 4th finger": [ + "HP:0009314" + ], + "fuse innermost bone of ring finger": [ + "HP:0009314" + ], + "fused innermost bone of ring finger": [ + "HP:0009314" + ], + "triangular shape proximal phalanx of the 4th finger": [ + "HP:0009315" + ], + "triangular shaped proximal phalanx of the 4th finger": [ + "HP:0009315" + ], + "triangular shape innermost bone of the 4th finger": [ + "HP:0009315" + ], + "triangular shaped innermost bone of the 4th finger": [ + "HP:0009315" + ], + "triangular shape innermost bone of the ring finger": [ + "HP:0009315" + ], + "triangular shaped innermost bone of the ring finger": [ + "HP:0009315" + ], + "abnormal 3rd finger phalanx morphology": [ + "HP:0009316" + ], + "abnormality of 3rd finger phalanx": [ + "HP:0009316" + ], + "abnormality of 3rd finger phalanges": [ + "HP:0009316" + ], + "abnormality of middle finger phalanx": [ + "HP:0009316" + ], + "abnormality of middle finger phalanges": [ + "HP:0009316" + ], + "abnormality of the middle finger bone": [ + "HP:0009316" + ], + "abnormality of the middle finger bones": [ + "HP:0009316" + ], + "abnormality of the phalanx of the 3rd finger": [ + "HP:0009316" + ], + "abnormality of the phalanges of the 3rd finger": [ + "HP:0009316" + ], + "deviation of the 3rd finger": [ + "HP:0009317" + ], + "deviate middle finger": [ + "HP:0009317" + ], + "deviated middle finger": [ + "HP:0009317" + ], + "aplasia / hypoplasia of the 3rd finger": [ + "HP:0009318" + ], + "absent / small middle finger": [ + "HP:0009318" + ], + "absent / underdevelop middle finger": [ + "HP:0009318" + ], + "absent / underdeveloped middle finger": [ + "HP:0009318" + ], + "joint contracture of the 3rd finger": [ + "HP:0009319" + ], + "camptodactyly of middle finger": [ + "HP:0009319" + ], + "abnormality of the epiphysis of the 3rd finger": [ + "HP:0009320" + ], + "abnormality of the epiphyses of the 3rd finger": [ + "HP:0009320" + ], + "abnormality of end part of the middle bone of the middle finger": [ + "HP:0009320" + ], + "absent epiphysis of the middle phalanx of the 3rd finger": [ + "HP:0009321" + ], + "absent end part of the middle bone of the middle finger": [ + "HP:0009321" + ], + "bracket epiphysis of the middle phalanx of the 3rd finger": [ + "HP:0009322" + ], + "bracket shape end part of the middle bone of the middle finger": [ + "HP:0009322" + ], + "bracket shaped end part of the middle bone of the middle finger": [ + "HP:0009322" + ], + "cone - shaped epiphysis of the middle phalanx of the 3rd finger": [ + "HP:0009323" + ], + "cone - shaped end part of the middle bone of the middle finger": [ + "HP:0009323" + ], + "enlarged epiphysis of the middle phalanx of the 3rd finger": [ + "HP:0009324" + ], + "enlarged end part of the middle bone of the middle finger": [ + "HP:0009324" + ], + "fragmentation of the epiphysis of the middle phalanx of the 3rd finger": [ + "HP:0009325" + ], + "fragmentation of end part of the middle bone of the middle finger": [ + "HP:0009325" + ], + "irregular epiphysis of the middle phalanx of the 3rd finger": [ + "HP:0009326" + ], + "irregular end part of the middle bone of the middle finger": [ + "HP:0009326" + ], + "ivory epiphysis of the middle phalanx of the 3rd finger": [ + "HP:0009327" + ], + "increase bone density of end part of the middle bone of the middle finger": [ + "HP:0009327" + ], + "increased bone density of end part of the middle bone of the middle finger": [ + "HP:0009327" + ], + "pseudoepiphysis of the middle phalanx of the 3rd finger": [ + "HP:0009328" + ], + "pseudoepiphyses of middle phalanx of middle - finger": [ + "HP:0009328" + ], + "small epiphysis of the middle phalanx of the 3rd finger": [ + "HP:0009329" + ], + "small end part of the middle bone of the middle finger": [ + "HP:0009329" + ], + "stippling of the epiphysis of the middle phalanx of the 3rd finger": [ + "HP:0009330" + ], + "speckled calcification in end part of the middle bone of the middle finger": [ + "HP:0009330" + ], + "speckled calcifications in end part of the middle bone of the middle finger": [ + "HP:0009330" + ], + "triangular epiphysis of the middle phalanx of the 3rd finger": [ + "HP:0009331" + ], + "delta - shaped epiphysis of the middle phalanx of the 3rd finger": [ + "HP:0009331" + ], + "triangular end part of the middle bone of the middle finger": [ + "HP:0009331" + ], + "abnormality of the epiphysis of the distal phalanx of the 3rd finger": [ + "HP:0009332" + ], + "abnormality of the end part of the outermost bone of the middle finger": [ + "HP:0009332" + ], + "abnormality of the epiphysis of the proximal phalanx of the 3rd finger": [ + "HP:0009333" + ], + "abnormality of the end part of the innermost bone of the middle finger": [ + "HP:0009333" + ], + "abnormality of the epiphysis of the middle phalanx of the 3rd finger": [ + "HP:0009334" + ], + "abnormality of the middle part of the middle bone of the middle finger": [ + "HP:0009334" + ], + "absent epiphysis of the distal phalanx of the 3rd finger": [ + "HP:0009335" + ], + "absent end part of the outermost bone of the middle finger": [ + "HP:0009335" + ], + "bracket epiphysis of the distal phalanx of the 3rd finger": [ + "HP:0009336" + ], + "bracket shape end part of the outermost bone of the middle finger": [ + "HP:0009336" + ], + "bracket shaped end part of the outermost bone of the middle finger": [ + "HP:0009336" + ], + "cone - shaped epiphysis of the distal phalanx of the 3rd finger": [ + "HP:0009337" + ], + "cone - shaped end part of the outermost bone of the middle finger": [ + "HP:0009337" + ], + "enlarged epiphysis of the distal phalanx of the 3rd finger": [ + "HP:0009338" + ], + "enlarged end part of the outermost bone of the 3rd finger": [ + "HP:0009338" + ], + "fragmentation of the epiphysis of the distal phalanx of the 3rd finger": [ + "HP:0009339" + ], + "fragmentation of end part of the outermost bone of the middle finger": [ + "HP:0009339" + ], + "irregular epiphysis of the distal phalanx of the 3rd finger": [ + "HP:0009340" + ], + "irregular end part of the outermost long bone of the middle finger": [ + "HP:0009340" + ], + "ivory epiphysis of the distal phalanx of the 3rd finger": [ + "HP:0009341" + ], + "increase bone density of end part of the outermost middle finger bone": [ + "HP:0009341" + ], + "increased bone density of end part of the outermost middle finger bone": [ + "HP:0009341" + ], + "pseudoepiphysis of the distal phalanx of the 3rd finger": [ + "HP:0009342" + ], + "pseudoepiphysis of the outermost bone of the middle finger": [ + "HP:0009342" + ], + "small epiphysis of the distal phalanx of the 3rd finger": [ + "HP:0009343" + ], + "small end part of the outermost long bone of the middle finger": [ + "HP:0009343" + ], + "stippling of the epiphysis of the distal phalanx of the 3rd finger": [ + "HP:0009344" + ], + "speckled calcification in end part of the outermost long bone of the middle finger": [ + "HP:0009344" + ], + "speckled calcifications in end part of the outermost long bone of the middle finger": [ + "HP:0009344" + ], + "triangular epiphysis of the distal phalanx of the 3rd finger": [ + "HP:0009345" + ], + "delta - shaped epiphysis of the distal phalanx of the 3rd finger": [ + "HP:0009345" + ], + "triangular end part of the outermost long bone of the middle finger": [ + "HP:0009345" + ], + "absent epiphysis of the proximal phalanx of the 3rd finger": [ + "HP:0009346" + ], + "absent end part of innermost long bone of the middle finger": [ + "HP:0009346" + ], + "bracket epiphysis of the proximal phalanx of the 3rd finger": [ + "HP:0009347" + ], + "bracket shape end part of innermost long bone of the middle finger": [ + "HP:0009347" + ], + "bracket shaped end part of innermost long bone of the middle finger": [ + "HP:0009347" + ], + "cone - shaped epiphysis of the proximal phalanx of the 3rd finger": [ + "HP:0009348" + ], + "cone - shaped end part of the innermost bone of the middle finger": [ + "HP:0009348" + ], + "enlarged epiphysis of the proximal phalanx of the 3rd finger": [ + "HP:0009349" + ], + "enlarged end part of innermost long bone of the middle finger": [ + "HP:0009349" + ], + "large epiphysis of proximal middle - finger phalanx": [ + "HP:0009349" + ], + "fragmentation of the epiphysis of the proximal phalanx of the 3rd finger": [ + "HP:0009350" + ], + "fragmentation of end part of innermost long bone of the middle finger": [ + "HP:0009350" + ], + "irregular epiphysis of the proximal phalanx of the 3rd finger": [ + "HP:0009351" + ], + "irregular end part of innermost long bone of the middle finger": [ + "HP:0009351" + ], + "ivory epiphysis of the proximal phalanx of the 3rd finger": [ + "HP:0009352" + ], + "increase bone density of end part of the innermost middle finger bone": [ + "HP:0009352" + ], + "increased bone density of end part of the innermost middle finger bone": [ + "HP:0009352" + ], + "pseudoepiphysis of the proximal phalanx of the 3rd finger": [ + "HP:0009353" + ], + "small epiphysis of the proximal phalanx of the 3rd finger": [ + "HP:0009354" + ], + "small end part of innermost long bone of the middle finger": [ + "HP:0009354" + ], + "stippling of the epiphysis of the proximal phalanx of the 3rd finger": [ + "HP:0009355" + ], + "speckled calcification in end part of innermost long bone of the middle finger": [ + "HP:0009355" + ], + "speckled calcifications in end part of innermost long bone of the middle finger": [ + "HP:0009355" + ], + "triangular epiphysis of the proximal phalanx of the 3rd finger": [ + "HP:0009356" + ], + "delta - shaped epiphysis of the proximal phalanx of the 3rd finger": [ + "HP:0009356" + ], + "triangular end part of innermost long bone of the middle finger": [ + "HP:0009356" + ], + "abnormality of the distal phalanx of the 3rd finger": [ + "HP:0009357" + ], + "abnormality of terminal phalanx of middle - finger": [ + "HP:0009357" + ], + "abnormality of the outermost bone of the 3rd finger": [ + "HP:0009357" + ], + "abnormality of the proximal phalanx of the 3rd finger": [ + "HP:0009358" + ], + "abnormal innermost bone of middle finger": [ + "HP:0009358" + ], + "abnormality of proximal middle - finger phalanx": [ + "HP:0009358" + ], + "type a brachydactyly": [ + "HP:0009370" + ], + "type a1 brachydactyly": [ + "HP:0009371" + ], + "type a2 brachydactyly": [ + "HP:0009372" + ], + "short index finger and second toe": [ + "HP:0009372" + ], + "short index fingers and second toes": [ + "HP:0009372" + ], + "type c brachydactyly": [ + "HP:0009373" + ], + "broad phalanx of the 5th finger": [ + "HP:0009374" + ], + "broad phalanges of the 5th finger": [ + "HP:0009374" + ], + "broad little finger bone": [ + "HP:0009374" + ], + "broad little finger bones": [ + "HP:0009374" + ], + "broad pinkie finger bone": [ + "HP:0009374" + ], + "broad pinkie finger bones": [ + "HP:0009374" + ], + "broad pinky finger bone": [ + "HP:0009374" + ], + "broad pinky finger bones": [ + "HP:0009374" + ], + "bullet - shaped phalanx of the 5th finger": [ + "HP:0009375" + ], + "bullet - shaped phalanges of the 5th finger": [ + "HP:0009375" + ], + "bullet - shape little finger bone": [ + "HP:0009375" + ], + "bullet - shaped little finger bones": [ + "HP:0009375" + ], + "bullet - shape pinkie finger bone": [ + "HP:0009375" + ], + "bullet - shaped pinkie finger bones": [ + "HP:0009375" + ], + "bullet - shape pinky finger bone": [ + "HP:0009375" + ], + "bullet - shaped pinky finger bones": [ + "HP:0009375" + ], + "aplasia / hypoplasia of the phalanx of the 5th finger": [ + "HP:0009376" + ], + "aplasia / hypoplasia of the phalanges of the 5th finger": [ + "HP:0009376" + ], + "absent / small little finger bone": [ + "HP:0009376" + ], + "absent / small little finger bones": [ + "HP:0009376" + ], + "absent / small pinkie finger bone": [ + "HP:0009376" + ], + "absent / small pinkie finger bones": [ + "HP:0009376" + ], + "absent / small pinky finger bone": [ + "HP:0009376" + ], + "absent / small pinky finger bones": [ + "HP:0009376" + ], + "absent / underdevelop pinky finger bone": [ + "HP:0009376" + ], + "absent / underdeveloped pinky finger bones": [ + "HP:0009376" + ], + "patchy sclerosis of 5th finger phalanx": [ + "HP:0009377" + ], + "patchy sclerosis of the phalanx of the 5th finger": [ + "HP:0009377" + ], + "patchy sclerosis of the phalanges of the 5th finger": [ + "HP:0009377" + ], + "uneven increase in bone density in little finger bone": [ + "HP:0009377" + ], + "uneven increase in bone density in pinkie finger bone": [ + "HP:0009377" + ], + "uneven increase in bone density in pinky finger bone": [ + "HP:0009377" + ], + "triangular shape phalanx of the 5th finger": [ + "HP:0009378" + ], + "triangular shaped phalanges of the 5th finger": [ + "HP:0009378" + ], + "triangular shape little finger bone": [ + "HP:0009378" + ], + "triangular shaped little finger bones": [ + "HP:0009378" + ], + "triangular shape pinkie finger bone": [ + "HP:0009378" + ], + "triangular shaped pinkie finger bones": [ + "HP:0009378" + ], + "triangular shape pinky finger bone": [ + "HP:0009378" + ], + "triangular shaped pinky finger bones": [ + "HP:0009378" + ], + "rhomboid or triangular shape 5th finger distal phalanx": [ + "HP:0009379" + ], + "rhomboid or triangular shaped 5th finger distal phalanx": [ + "HP:0009379" + ], + "rhomboid or triangular shape little finger bone": [ + "HP:0009379" + ], + "rhomboid or triangular shaped little finger bone": [ + "HP:0009379" + ], + "rhomboid or triangular shape pinkie finger bone": [ + "HP:0009379" + ], + "rhomboid or triangular shaped pinkie finger bone": [ + "HP:0009379" + ], + "rhomboid or triangular shape pinky finger bone": [ + "HP:0009379" + ], + "rhomboid or triangular shaped pinky finger bone": [ + "HP:0009379" + ], + "aplasia of the finger": [ + "HP:0009380" + ], + "aplasia of the fingers": [ + "HP:0009380" + ], + "absent finger": [ + "HP:0009380" + ], + "absent fingers": [ + "HP:0009380" + ], + "short finger": [ + "HP:0009381" + ], + "hypoplastic digit": [ + "HP:0009381" + ], + "hypoplastic digits": [ + "HP:0009381" + ], + "hypoplastic finger": [ + "HP:0009381" + ], + "hypoplastic fingers": [ + "HP:0009381" + ], + "hypoplastic / small finger": [ + "HP:0009381" + ], + "hypoplastic / small fingers": [ + "HP:0009381" + ], + "stubby finger": [ + "HP:0009381" + ], + "stubby fingers": [ + "HP:0009381" + ], + "absent epiphysis of the 5th finger": [ + "HP:0009382" + ], + "absent epiphyses of the 5th finger": [ + "HP:0009382" + ], + "absent end part of little finger bone": [ + "HP:0009382" + ], + "absent end part of pinkie finger bone": [ + "HP:0009382" + ], + "absent end part of pinky finger bone": [ + "HP:0009382" + ], + "bracket epiphysis of the 5th finger": [ + "HP:0009383" + ], + "bracket epiphyses of the 5th finger": [ + "HP:0009383" + ], + "bracket shape end part of little finger bone": [ + "HP:0009383" + ], + "bracket shaped end part of little finger bone": [ + "HP:0009383" + ], + "bracket shape end part of pinkie finger bone": [ + "HP:0009383" + ], + "bracket shaped end part of pinkie finger bone": [ + "HP:0009383" + ], + "bracket shape end part of pinky finger bone": [ + "HP:0009383" + ], + "bracket shaped end part of pinky finger bone": [ + "HP:0009383" + ], + "cone - shaped epiphysis of the 5th finger": [ + "HP:0009384" + ], + "cone - shaped epiphyses of the 5th finger": [ + "HP:0009384" + ], + "cone - shaped end part of the little finger bone": [ + "HP:0009384" + ], + "cone - shaped end part of the little finger bones": [ + "HP:0009384" + ], + "cone - shaped end part of the pinkie finger bone": [ + "HP:0009384" + ], + "cone - shaped end part of the pinkie finger bones": [ + "HP:0009384" + ], + "cone - shaped end part of the pinky finger bone": [ + "HP:0009384" + ], + "cone - shaped end part of the pinky finger bones": [ + "HP:0009384" + ], + "enlarged epiphysis of the 5th finger": [ + "HP:0009385" + ], + "enlarged epiphyses of the 5th finger": [ + "HP:0009385" + ], + "enlarged end part of the little finger bone": [ + "HP:0009385" + ], + "enlarged end part of the little finger bones": [ + "HP:0009385" + ], + "enlarged end part of the pinkie finger bone": [ + "HP:0009385" + ], + "enlarged end part of the pinkie finger bones": [ + "HP:0009385" + ], + "enlarged end part of the pinky finger bone": [ + "HP:0009385" + ], + "enlarged end part of the pinky finger bones": [ + "HP:0009385" + ], + "fragmentation of the epiphysis of the 5th finger": [ + "HP:0009386" + ], + "fragmentation of the epiphyses of the 5th finger": [ + "HP:0009386" + ], + "fragmentation of the end part of the little finger bone": [ + "HP:0009386" + ], + "fragmentation of the end part of the little finger bones": [ + "HP:0009386" + ], + "fragmentation of the end part of the pinkie finger bone": [ + "HP:0009386" + ], + "fragmentation of the end part of the pinkie finger bones": [ + "HP:0009386" + ], + "fragmentation of the end part of the pinky finger bone": [ + "HP:0009386" + ], + "fragmentation of the end part of the pinky finger bones": [ + "HP:0009386" + ], + "irregular epiphysis of the 5th finger": [ + "HP:0009387" + ], + "irregular epiphyses of the 5th finger": [ + "HP:0009387" + ], + "irregular end part of the little finger bone": [ + "HP:0009387" + ], + "irregular end part of the little finger bones": [ + "HP:0009387" + ], + "irregular end part of the pinkie finger bone": [ + "HP:0009387" + ], + "irregular end part of the pinkie finger bones": [ + "HP:0009387" + ], + "irregular end part of the pinky finger bone": [ + "HP:0009387" + ], + "irregular end part of the pinky finger bones": [ + "HP:0009387" + ], + "ivory epiphysis of the 5th finger": [ + "HP:0009388" + ], + "ivory epiphyses of the 5th finger": [ + "HP:0009388" + ], + "increase bone density of end part of the little finger": [ + "HP:0009388" + ], + "increased bone density of end part of the little finger": [ + "HP:0009388" + ], + "increase bone density of end part of the pinkie finger": [ + "HP:0009388" + ], + "increased bone density of end part of the pinkie finger": [ + "HP:0009388" + ], + "increase bone density of end part of the pinky finger": [ + "HP:0009388" + ], + "increased bone density of end part of the pinky finger": [ + "HP:0009388" + ], + "pseudoepiphyses of the 5th finger": [ + "HP:0009389" + ], + "small epiphysis of the 5th finger": [ + "HP:0009390" + ], + "small epiphyses of the 5th finger": [ + "HP:0009390" + ], + "small end part of little finger bone": [ + "HP:0009390" + ], + "small end part of pinkie finger bone": [ + "HP:0009390" + ], + "small end part of pinky finger bone": [ + "HP:0009390" + ], + "stippling of the epiphysis of the 5th finger": [ + "HP:0009391" + ], + "stippling of the epiphyses of the 5th finger": [ + "HP:0009391" + ], + "speckled calcification in end part of little finger bone": [ + "HP:0009391" + ], + "speckled calcifications in end part of little finger bone": [ + "HP:0009391" + ], + "speckled calcification in end part of pinkie finger bone": [ + "HP:0009391" + ], + "speckled calcifications in end part of pinkie finger bone": [ + "HP:0009391" + ], + "speckled calcification in end part of pinky finger bone": [ + "HP:0009391" + ], + "speckled calcifications in end part of pinky finger bone": [ + "HP:0009391" + ], + "triangular epiphysis of the 5th finger": [ + "HP:0009392" + ], + "triangular epiphyses of the 5th finger": [ + "HP:0009392" + ], + "delta - shaped epiphysis of the 5th finger": [ + "HP:0009392" + ], + "delta - shaped epiphyses of the 5th finger": [ + "HP:0009392" + ], + "triangular end part of the little finger": [ + "HP:0009392" + ], + "triangular end part of the pinkie finger": [ + "HP:0009392" + ], + "triangular end part of the pinky finger": [ + "HP:0009392" + ], + "absent epiphysis of the 4th finger": [ + "HP:0009393" + ], + "absent epiphyses of the 4th finger": [ + "HP:0009393" + ], + "absent end part of the ring finger bone": [ + "HP:0009393" + ], + "bracket epiphysis of the 4th finger": [ + "HP:0009394" + ], + "bracket epiphyses of the 4th finger": [ + "HP:0009394" + ], + "bracket shape end part of ring finger bone": [ + "HP:0009394" + ], + "bracket shaped end part of ring finger bones": [ + "HP:0009394" + ], + "cone - shaped epiphysis of the 4th finger": [ + "HP:0009395" + ], + "cone - shaped epiphyses of the 4th finger": [ + "HP:0009395" + ], + "cone - shaped end part of the ring finger bone": [ + "HP:0009395" + ], + "cone - shaped end part of the ring finger bones": [ + "HP:0009395" + ], + "enlarged epiphysis of the 4th finger": [ + "HP:0009396" + ], + "enlarged epiphyses of the 4th finger": [ + "HP:0009396" + ], + "enlarged end part of the ring finger bone": [ + "HP:0009396" + ], + "enlarged end part of the ring finger bones": [ + "HP:0009396" + ], + "fragmentation of the epiphysis of the 4th finger": [ + "HP:0009397" + ], + "fragmentation of the epiphyses of the 4th finger": [ + "HP:0009397" + ], + "fragmentation of the end part of the ring finger bone": [ + "HP:0009397" + ], + "fragmentation of the end part of the ring finger bones": [ + "HP:0009397" + ], + "irregular epiphysis of the 4th finger": [ + "HP:0009398" + ], + "irregular epiphyses of the 4th finger": [ + "HP:0009398" + ], + "irregular end part of the ring finger bone": [ + "HP:0009398" + ], + "irregular end part of the ring finger bones": [ + "HP:0009398" + ], + "ivory epiphysis of the 4th finger": [ + "HP:0009399" + ], + "ivory epiphyses of the 4th finger": [ + "HP:0009399" + ], + "increase bone density of end part of the ring finger bone": [ + "HP:0009399" + ], + "increased bone density of end part of the ring finger bone": [ + "HP:0009399" + ], + "pseudoepiphyses of the 4th finger": [ + "HP:0009400" + ], + "small epiphysis of the 4th finger": [ + "HP:0009401" + ], + "small epiphyses of the 4th finger": [ + "HP:0009401" + ], + "small end part of ring finger bone": [ + "HP:0009401" + ], + "stippling of the epiphysis of the 4th finger": [ + "HP:0009402" + ], + "stippling of the epiphyses of the 4th finger": [ + "HP:0009402" + ], + "speckled calcification in end part of ring finger bone": [ + "HP:0009402" + ], + "speckled calcifications in end part of ring finger bone": [ + "HP:0009402" + ], + "triangular epiphysis of the 4th finger": [ + "HP:0009403" + ], + "triangular epiphyses of the 4th finger": [ + "HP:0009403" + ], + "delta - shaped epiphysis of the 4th finger": [ + "HP:0009403" + ], + "delta - shaped epiphyses of the 4th finger": [ + "HP:0009403" + ], + "triangular end part of ring finger bone": [ + "HP:0009403" + ], + "broad phalanx of the 4th finger": [ + "HP:0009404" + ], + "broad phalanges of the 4th finger": [ + "HP:0009404" + ], + "broad bone of ring finger": [ + "HP:0009404" + ], + "broad bones of ring finger": [ + "HP:0009404" + ], + "bullet - shaped phalanx of the 4th finger": [ + "HP:0009405" + ], + "bullet - shaped phalanges of the 4th finger": [ + "HP:0009405" + ], + "bullet - shaped of bone of ring finger": [ + "HP:0009405" + ], + "patchy sclerosis of 4th finger phalanx": [ + "HP:0009406" + ], + "patchy sclerosis of the phalanx of the 4th finger": [ + "HP:0009406" + ], + "patchy sclerosis of the phalanges of the 4th finger": [ + "HP:0009406" + ], + "uneven increase in bone density in ring finger bone": [ + "HP:0009406" + ], + "triangular shape phalanx of the 4th finger": [ + "HP:0009407" + ], + "triangular shaped phalanges of the 4th finger": [ + "HP:0009407" + ], + "triangular shape bone of ring finger": [ + "HP:0009407" + ], + "triangular shaped bone of ring finger": [ + "HP:0009407" + ], + "aplasia / hypoplasia of the phalanx of the 4th finger": [ + "HP:0009408" + ], + "aplasia / hypoplasia of the phalanges of the 4th finger": [ + "HP:0009408" + ], + "absent / small ring finger bones": [ + "HP:0009408" + ], + "absent / underdeveloped ring finger bones": [ + "HP:0009408" + ], + "absent epiphysis of the 3rd finger": [ + "HP:0009410" + ], + "absent epiphyses of the 3rd finger": [ + "HP:0009410" + ], + "absent end part of middle finger bone": [ + "HP:0009410" + ], + "bracket epiphysis of the 3rd finger": [ + "HP:0009411" + ], + "bracket epiphyses of the 3rd finger": [ + "HP:0009411" + ], + "bracket shape end part of middle finger bone": [ + "HP:0009411" + ], + "bracket shaped end part of middle finger bone": [ + "HP:0009411" + ], + "cone - shaped epiphysis of the 3rd finger": [ + "HP:0009412" + ], + "cone - shaped epiphyses of the 3rd finger": [ + "HP:0009412" + ], + "cone - shaped end part of middle finger bone": [ + "HP:0009412" + ], + "enlarged epiphysis of the 3rd finger": [ + "HP:0009413" + ], + "enlarged epiphyses of the 3rd finger": [ + "HP:0009413" + ], + "enlarged end part of middle finger bone": [ + "HP:0009413" + ], + "fragmentation of the epiphysis of the 3rd finger": [ + "HP:0009414" + ], + "fragmentation of the epiphyses of the 3rd finger": [ + "HP:0009414" + ], + "fragmentation of end part of middle finger bone": [ + "HP:0009414" + ], + "irregular epiphysis of the 3rd finger": [ + "HP:0009415" + ], + "irregular epiphyses of the 3rd finger": [ + "HP:0009415" + ], + "irregular end part of middle finger bone": [ + "HP:0009415" + ], + "ivory epiphysis of the 3rd finger": [ + "HP:0009416" + ], + "ivory epiphyses of the 3rd finger": [ + "HP:0009416" + ], + "increase bone density of end part of the middle finger bone": [ + "HP:0009416" + ], + "increased bone density of end part of the middle finger bone": [ + "HP:0009416" + ], + "pseudoepiphyses of the 3rd finger": [ + "HP:0009417" + ], + "pseudoepiphyses of middle finger phalanx": [ + "HP:0009417" + ], + "pseudoepiphyses of middle finger phalanges": [ + "HP:0009417" + ], + "small epiphysis of the 3rd finger": [ + "HP:0009418" + ], + "small epiphyses of the 3rd finger": [ + "HP:0009418" + ], + "small end part of middle finger bone": [ + "HP:0009418" + ], + "stippling of the epiphysis of the 3rd finger": [ + "HP:0009419" + ], + "stippling of the epiphyses of the 3rd finger": [ + "HP:0009419" + ], + "speckled calcification in end part of middle finger bone": [ + "HP:0009419" + ], + "speckled calcifications in end part of middle finger bone": [ + "HP:0009419" + ], + "triangular epiphysis of the 3rd finger": [ + "HP:0009420" + ], + "triangular epiphyses of the 3rd finger": [ + "HP:0009420" + ], + "delta - shaped epiphysis of the 3rd finger": [ + "HP:0009420" + ], + "delta - shaped epiphyses of the 3rd finger": [ + "HP:0009420" + ], + "triangular end part of middle finger bone": [ + "HP:0009420" + ], + "aplasia / hypoplasia of the distal phalanx of the 3rd finger": [ + "HP:0009421" + ], + "absent / small outermost middle finger bone": [ + "HP:0009421" + ], + "absent / underdevelop outermost middle finger bone": [ + "HP:0009421" + ], + "absent / underdeveloped outermost middle finger bone": [ + "HP:0009421" + ], + "broad distal phalanx of the 3rd finger": [ + "HP:0009422" + ], + "broad outermost bone of middle finger": [ + "HP:0009422" + ], + "bullet - shaped distal phalanx of the 3rd finger": [ + "HP:0009423" + ], + "bullet - shape outermost bone of the middle finger": [ + "HP:0009423" + ], + "bullet - shaped outermost bone of the middle finger": [ + "HP:0009423" + ], + "osteolytic defect of the distal phalanx of the 3rd finger": [ + "HP:0009424" + ], + "osteolytic defects of the distal phalanx of the 3rd finger": [ + "HP:0009424" + ], + "lytic defect of terminal phalanx of middle finger": [ + "HP:0009424" + ], + "patchy sclerosis of the distal phalanx of the 3rd finger": [ + "HP:0009425" + ], + "uneven increase in bone density in the outermost bone of the 3rd finger": [ + "HP:0009425" + ], + "distal / middle symphalangism of 3rd finger": [ + "HP:0009426" + ], + "fuse outermost and middle bone of middle finger": [ + "HP:0009426" + ], + "fused outermost and middle bones of middle finger": [ + "HP:0009426" + ], + "symphalangism of the distal and middle phalanx of the 3rd finger": [ + "HP:0009426" + ], + "symphalangism of the distal and middle phalanges of the 3rd finger": [ + "HP:0009426" + ], + "triangular shape distal phalanx of the 3rd finger": [ + "HP:0009427" + ], + "triangular shaped distal phalanx of the 3rd finger": [ + "HP:0009427" + ], + "triangular shape outermost bone of the middle finger": [ + "HP:0009427" + ], + "triangular shaped outermost bone of the middle finger": [ + "HP:0009427" + ], + "curve distal phalanx of the 3rd finger": [ + "HP:0009428" + ], + "curved distal phalanx of the 3rd finger": [ + "HP:0009428" + ], + "curve outermost bone of the 3rd finger": [ + "HP:0009428" + ], + "curved outermost bone of the 3rd finger": [ + "HP:0009428" + ], + "aplasia of the distal phalanx of the 3rd finger": [ + "HP:0009429" + ], + "absent of the outermost bone of the middle finger": [ + "HP:0009429" + ], + "broad middle phalanx of the 3rd finger": [ + "HP:0009430" + ], + "broad middle bone of middle finger": [ + "HP:0009430" + ], + "wide / broad middle phalanx of middle - finger": [ + "HP:0009430" + ], + "bullet - shape middle phalanx of the 3rd finger": [ + "HP:0009431" + ], + "bullet - shaped middle phalanx of the 3rd finger": [ + "HP:0009431" + ], + "bullet - shape middle bone of middle finger": [ + "HP:0009431" + ], + "bullet - shaped middle bone of middle finger": [ + "HP:0009431" + ], + "curve middle phalanx of the 3rd finger": [ + "HP:0009432" + ], + "curved middle phalanx of the 3rd finger": [ + "HP:0009432" + ], + "curve middle bone of the middle finger": [ + "HP:0009432" + ], + "curved middle bone of the middle finger": [ + "HP:0009432" + ], + "osteolytic defect of the middle phalanx of the 3rd finger": [ + "HP:0009433" + ], + "osteolytic defects of the middle phalanx of the 3rd finger": [ + "HP:0009433" + ], + "patchy sclerosis of the middle phalanx of the 3rd finger": [ + "HP:0009434" + ], + "uneven increase in bone density in the middle bone of the middle finger": [ + "HP:0009434" + ], + "symphalangism of middle phalanx of 3rd finger": [ + "HP:0009435" + ], + "fuse middle bone of middle finger": [ + "HP:0009435" + ], + "fused middle bone of middle finger": [ + "HP:0009435" + ], + "triangular shape middle phalanx of the 3rd finger": [ + "HP:0009436" + ], + "triangular shaped middle phalanx of the 3rd finger": [ + "HP:0009436" + ], + "triangular shape middle bone of the middle finger": [ + "HP:0009436" + ], + "triangular shaped middle bone of the middle finger": [ + "HP:0009436" + ], + "aplasia / hypoplasia of the middle phalanx of the 3rd finger": [ + "HP:0009437" + ], + "absent / small middle bone of the middle finger": [ + "HP:0009437" + ], + "absent / underdevelop middle bone of the middle finger": [ + "HP:0009437" + ], + "absent / underdeveloped middle bone of the middle finger": [ + "HP:0009437" + ], + "absent middle phalanx of 3rd finger": [ + "HP:0009438" + ], + "absent middle bone of middle finger": [ + "HP:0009438" + ], + "absent middle phalanx of middle finger": [ + "HP:0009438" + ], + "aplasia of the middle phalanx of the 3rd finger": [ + "HP:0009438" + ], + "short middle phalanx of the 3rd finger": [ + "HP:0009439" + ], + "brachymesophalangy iii ( finger )": [ + "HP:0009439" + ], + "hypoplastic / small middle phalanx of the 3rd finger": [ + "HP:0009439" + ], + "short middle bone of middle finger": [ + "HP:0009439" + ], + "broad phalanx of the 3rd finger": [ + "HP:0009440" + ], + "broad phalanges of the 3rd finger": [ + "HP:0009440" + ], + "wide bone of middle finger": [ + "HP:0009440" + ], + "wide bones of middle finger": [ + "HP:0009440" + ], + "wide / broad middle finger phalanx": [ + "HP:0009440" + ], + "wide / broad middle finger phalanges": [ + "HP:0009440" + ], + "bullet - shaped phalanx of the 3rd finger": [ + "HP:0009441" + ], + "bullet - shaped phalanges of the 3rd finger": [ + "HP:0009441" + ], + "bullet - shaped bone of middle finger": [ + "HP:0009441" + ], + "bullet - shaped bones of middle finger": [ + "HP:0009441" + ], + "curve phalanx of the 3rd finger": [ + "HP:0009442" + ], + "curved phalanges of the 3rd finger": [ + "HP:0009442" + ], + "curve bone of middle finger": [ + "HP:0009442" + ], + "curved bones of middle finger": [ + "HP:0009442" + ], + "osteolytic defect of the phalanx of the 3rd finger": [ + "HP:0009443" + ], + "osteolytic defects of the phalanges of the 3rd finger": [ + "HP:0009443" + ], + "lytic defect of middle finger phalanx": [ + "HP:0009443" + ], + "lytic defects of middle finger phalanges": [ + "HP:0009443" + ], + "patchy sclerosis of 3rd finger phalanx": [ + "HP:0009444" + ], + "patchy sclerosis of middle finger phalanx": [ + "HP:0009444" + ], + "patchy sclerosis of middle finger phalanges": [ + "HP:0009444" + ], + "patchy sclerosis of the phalanx of the 3rd finger": [ + "HP:0009444" + ], + "patchy sclerosis of the phalanges of the 3rd finger": [ + "HP:0009444" + ], + "uneven increase in bone density in middle finger bone": [ + "HP:0009444" + ], + "symphalangism of the 3rd finger": [ + "HP:0009445" + ], + "fuse middle finger": [ + "HP:0009445" + ], + "fused middle finger": [ + "HP:0009445" + ], + "triangular shape phalanx of the 3rd finger": [ + "HP:0009446" + ], + "triangular shaped phalanges of the 3rd finger": [ + "HP:0009446" + ], + "triangular shape bone of the middle finger": [ + "HP:0009446" + ], + "triangular shaped bone of the middle finger": [ + "HP:0009446" + ], + "aplasia / hypoplasia of the phalanx of the 3rd finger": [ + "HP:0009447" + ], + "aplasia / hypoplasia of the phalanges of the 3rd finger": [ + "HP:0009447" + ], + "absent / small middle finger bone": [ + "HP:0009447" + ], + "absent / underdevelop middle finger bone": [ + "HP:0009447" + ], + "absent / underdeveloped middle finger bone": [ + "HP:0009447" + ], + "hypoplastic middle finger phalanx": [ + "HP:0009447" + ], + "hypoplastic middle finger phalanges": [ + "HP:0009447" + ], + "short middle finger phalanx": [ + "HP:0009447" + ], + "short middle finger phalanges": [ + "HP:0009447" + ], + "small middle finger phalanx": [ + "HP:0009447" + ], + "small middle finger phalanges": [ + "HP:0009447" + ], + "obsolete aplasia of the phalanx of the 3rd finger": [ + "HP:0009448" + ], + "obsolete aplasia of the phalanges of the 3rd finger": [ + "HP:0009448" + ], + "obsolete hypoplastic / small phalanx of the 3rd finger": [ + "HP:0009449" + ], + "obsolete hypoplastic / small phalanges of the 3rd finger": [ + "HP:0009449" + ], + "broad proximal phalanx of the 3rd finger": [ + "HP:0009450" + ], + "broad innermost bone of middle finger": [ + "HP:0009450" + ], + "bullet - shape proximal phalanx of the 3rd finger": [ + "HP:0009451" + ], + "bullet - shaped proximal phalanx of the 3rd finger": [ + "HP:0009451" + ], + "bullet - shape innermost bone of the middle finger": [ + "HP:0009451" + ], + "bullet - shaped innermost bone of the middle finger": [ + "HP:0009451" + ], + "curve proximal phalanx of the 3rd finger": [ + "HP:0009452" + ], + "curved proximal phalanx of the 3rd finger": [ + "HP:0009452" + ], + "curve innermost bone of middle finger": [ + "HP:0009452" + ], + "curved innermost bone of middle finger": [ + "HP:0009452" + ], + "osteolytic defect of the proximal phalanx of the 3rd finger": [ + "HP:0009453" + ], + "osteolytic defects of the proximal phalanx of the 3rd finger": [ + "HP:0009453" + ], + "patchy sclerosis of the proximal phalanx of the 3rd finger": [ + "HP:0009454" + ], + "uneven increase in bone density in the innermost bone of the middle finger": [ + "HP:0009454" + ], + "symphalangism affect the proximal phalanx of the 3rd finger": [ + "HP:0009455" + ], + "symphalangism affecting the proximal phalanx of the 3rd finger": [ + "HP:0009455" + ], + "fuse innermost bone of middle finger": [ + "HP:0009455" + ], + "fused innermost bone of middle finger": [ + "HP:0009455" + ], + "triangular shape proximal phalanx of the 3rd finger": [ + "HP:0009456" + ], + "triangular shaped proximal phalanx of the 3rd finger": [ + "HP:0009456" + ], + "triangular shape innermost bone of middle finger": [ + "HP:0009456" + ], + "triangular shaped innermost bone of middle finger": [ + "HP:0009456" + ], + "aplasia / hypoplasia of the proximal phalanx of the 3rd finger": [ + "HP:0009457" + ], + "absent / small innermost bone of middle finger": [ + "HP:0009457" + ], + "absent / underdevelop innermost bone of middle finger": [ + "HP:0009457" + ], + "absent / underdeveloped innermost bone of middle finger": [ + "HP:0009457" + ], + "aplasia of the proximal phalanx of the 3rd finger": [ + "HP:0009458" + ], + "absent innermost bone of middle finger": [ + "HP:0009458" + ], + "short proximal phalanx of the 3rd finger": [ + "HP:0009459" + ], + "hypoplastic / small proximal phalanx of the 3rd finger": [ + "HP:0009459" + ], + "short innermost bone of middle finger": [ + "HP:0009459" + ], + "short proximal middle - finger phalanx": [ + "HP:0009459" + ], + "short proximal phalanx of the third finger": [ + "HP:0009459" + ], + "small proximal middle - finger phalanx": [ + "HP:0009459" + ], + "aplasia of the 3rd finger": [ + "HP:0009460" + ], + "absent middle finger": [ + "HP:0009460" + ], + "short 3rd finger": [ + "HP:0009461" + ], + "hypoplastic / small 3rd finger": [ + "HP:0009461" + ], + "short middle finger": [ + "HP:0009461" + ], + "radial deviation of the 3rd finger": [ + "HP:0009462" + ], + "inward turn middle finger": [ + "HP:0009462" + ], + "inward turned middle finger": [ + "HP:0009462" + ], + "ulnar deviation of the 3rd finger": [ + "HP:0009463" + ], + "ulnar deviation of middle finger": [ + "HP:0009463" + ], + "ulnar deviation of middle fingers": [ + "HP:0009463" + ], + "ulnar deviation of the 2nd finger": [ + "HP:0009464" + ], + "medially deviate index finger": [ + "HP:0009464" + ], + "medially deviated index finger": [ + "HP:0009464" + ], + "second finger ulnar deviation": [ + "HP:0009464" + ], + "ulnar angulation of the index finger": [ + "HP:0009464" + ], + "ulnar deviation of index finger": [ + "HP:0009464" + ], + "ulnar deviation of index fingers": [ + "HP:0009464" + ], + "ulnar deviation of finger": [ + "HP:0009465" + ], + "finger bend toward pinky": [ + "HP:0009465" + ], + "finger bends toward pinky": [ + "HP:0009465" + ], + "ulnar drift": [ + "HP:0009465" + ], + "radial deviation of finger": [ + "HP:0009466" + ], + "radially deviate finger": [ + "HP:0009466" + ], + "radially deviated fingers": [ + "HP:0009466" + ], + "radially deviate phalanx": [ + "HP:0009466" + ], + "radially deviated phalanges": [ + "HP:0009466" + ], + "radial deviation of the 2nd finger": [ + "HP:0009467" + ], + "radially deviate index finger": [ + "HP:0009467" + ], + "radially deviated index finger": [ + "HP:0009467" + ], + "deviation of the 2nd finger": [ + "HP:0009468" + ], + "deviate index finger": [ + "HP:0009468" + ], + "deviated index finger": [ + "HP:0009468" + ], + "displaced index finger": [ + "HP:0009468" + ], + "contracture of the distal interphalangeal joint of the 3rd finger": [ + "HP:0009469" + ], + "contracture of the outermost hinge joint of the 3rd finger": [ + "HP:0009469" + ], + "contracture of the metacarpophalangeal joint of the 3rd finger": [ + "HP:0009470" + ], + "contracture of the proximal interphalangeal joint of the 3rd finger": [ + "HP:0009471" + ], + "camptodactyly of the 3rd finger": [ + "HP:0009471" + ], + "camptodactyly of the third finger": [ + "HP:0009471" + ], + "joint contracture of the hand": [ + "HP:0009473" + ], + "contracture involve the hand": [ + "HP:0009473" + ], + "contractures involving the hands": [ + "HP:0009473" + ], + "contracture of the hand": [ + "HP:0009473" + ], + "contractures of the hands": [ + "HP:0009473" + ], + "proximal / middle symphalangism of 4th finger": [ + "HP:0009477" + ], + "fuse innermost and middle bone of fourth finger": [ + "HP:0009477" + ], + "fused innermost and middle bone of fourth finger": [ + "HP:0009477" + ], + "symphalangism of the proximal phalanx of the 4th finger with the 4th metacarpal": [ + "HP:0009478" + ], + "fuse innermost bone of ring finger with 4th long bone of hand": [ + "HP:0009478" + ], + "fused innermost bone of ring finger with 4th long bone of hand": [ + "HP:0009478" + ], + "proximal / middle symphalangism of 3rd finger": [ + "HP:0009482" + ], + "fuse of innermost and middle bone of middle finger": [ + "HP:0009482" + ], + "fused of innermost and middle bones of middle finger": [ + "HP:0009482" + ], + "symphalangism of the proximal phalanx of the 3rd finger with the 3rd metacarpal": [ + "HP:0009483" + ], + "fuse innermost bone of middle finger with middle long bone of hand": [ + "HP:0009483" + ], + "fused innermost bones of middle finger with middle long bone of hand": [ + "HP:0009483" + ], + "deviation of the hand or of finger of the hand": [ + "HP:0009484" + ], + "deviation of the hand or of fingers of the hand": [ + "HP:0009484" + ], + "displaced hand or finger of the hand": [ + "HP:0009484" + ], + "displaced hand or fingers of the hand": [ + "HP:0009484" + ], + "radial deviation of the hand or of finger of the hand": [ + "HP:0009485" + ], + "radial deviation of the hand or of fingers of the hand": [ + "HP:0009485" + ], + "radial deviation of the hand": [ + "HP:0009486" + ], + "radial deviation of hand": [ + "HP:0009486" + ], + "radial deviation of hands": [ + "HP:0009486" + ], + "ulnar deviation of the hand": [ + "HP:0009487" + ], + "ulnar deviation of hand": [ + "HP:0009487" + ], + "ulnar deviation of hands": [ + "HP:0009487" + ], + "ulnar deviation of the hands": [ + "HP:0009487" + ], + "absent epiphysis of the 2nd finger": [ + "HP:0009488" + ], + "absent epiphyses of the 2nd finger": [ + "HP:0009488" + ], + "absent end part of index finger": [ + "HP:0009488" + ], + "bracket epiphysis of the 2nd finger": [ + "HP:0009489" + ], + "bracket epiphyses of the 2nd finger": [ + "HP:0009489" + ], + "bracket shape end part of index finger": [ + "HP:0009489" + ], + "bracket shaped end part of index finger": [ + "HP:0009489" + ], + "bracket - epiphysis of index finger": [ + "HP:0009489" + ], + "bracket - epiphyses of index finger": [ + "HP:0009489" + ], + "cone - shaped epiphysis of the 2nd finger": [ + "HP:0009490" + ], + "cone - shaped epiphyses of the 2nd finger": [ + "HP:0009490" + ], + "cone - shaped end part of the index finger": [ + "HP:0009490" + ], + "enlarged epiphysis of the 2nd finger": [ + "HP:0009491" + ], + "enlarged epiphyses of the 2nd finger": [ + "HP:0009491" + ], + "enlarged end part of the index finger": [ + "HP:0009491" + ], + "fragmentation of the epiphysis of the 2nd finger": [ + "HP:0009492" + ], + "fragmentation of the epiphyses of the 2nd finger": [ + "HP:0009492" + ], + "fragmentation of end part of the index finger": [ + "HP:0009492" + ], + "irregular epiphysis of the 2nd finger": [ + "HP:0009493" + ], + "irregular epiphyses of the 2nd finger": [ + "HP:0009493" + ], + "irregular end part of the index finger": [ + "HP:0009493" + ], + "ivory epiphysis of the 2nd finger": [ + "HP:0009494" + ], + "ivory epiphyses of the 2nd finger": [ + "HP:0009494" + ], + "increase bone density of end part of the index finger bone": [ + "HP:0009494" + ], + "increased bone density of end part of the index finger bone": [ + "HP:0009494" + ], + "pseudoepiphyses of the 2nd finger": [ + "HP:0009495" + ], + "accessory index finger phalanx": [ + "HP:0009495" + ], + "accessory index finger phalanges": [ + "HP:0009495" + ], + "small epiphysis of the 2nd finger": [ + "HP:0009496" + ], + "small epiphyses of the 2nd finger": [ + "HP:0009496" + ], + "small end part of the index finger": [ + "HP:0009496" + ], + "stippling of the epiphysis of the 2nd finger": [ + "HP:0009497" + ], + "stippling of the epiphyses of the 2nd finger": [ + "HP:0009497" + ], + "speckled calcification in end part of the index finger": [ + "HP:0009497" + ], + "speckled calcifications in end part of the index finger": [ + "HP:0009497" + ], + "triangular epiphysis of the 2nd finger": [ + "HP:0009498" + ], + "triangular epiphyses of the 2nd finger": [ + "HP:0009498" + ], + "triangular end part of the index finger": [ + "HP:0009498" + ], + "abnormality of the epiphysis of the distal phalanx of the 2nd finger": [ + "HP:0009499" + ], + "abnormality of the end part of the outermost bone of the index finger": [ + "HP:0009499" + ], + "epiphyseal abnormality of terminal index finger phalanx": [ + "HP:0009499" + ], + "abnormality of the epiphysis of the middle phalanx of the 2nd finger": [ + "HP:0009500" + ], + "abnormality of end part of the middle bone of the index finger": [ + "HP:0009500" + ], + "epiphyseal abnormality of middle phalanx of the 2nd finger": [ + "HP:0009500" + ], + "abnormality of the epiphysis of the proximal phalanx of the 2nd finger": [ + "HP:0009501" + ], + "epiphyseal abnormality of the proximal phalanx of the 2nd finger": [ + "HP:0009501" + ], + "absent epiphysis of the distal phalanx of the 2nd finger": [ + "HP:0009502" + ], + "absent end part of the outermost bone of the index finger": [ + "HP:0009502" + ], + "absent ossification / absent epiphysis of terminal index finger phalanx": [ + "HP:0009502" + ], + "bracket epiphysis of the distal phalanx of the 2nd finger": [ + "HP:0009503" + ], + "bracket shape end part of the outermost bone of the index finger": [ + "HP:0009503" + ], + "bracket shaped end part of the outermost bone of the index finger": [ + "HP:0009503" + ], + "cone - shaped epiphysis of the distal phalanx of the 2nd finger": [ + "HP:0009504" + ], + "cone - shaped end part of the outermost bone of the index finger": [ + "HP:0009504" + ], + "enlarged epiphysis of the distal phalanx of the 2nd finger": [ + "HP:0009505" + ], + "enlarged end part of the outermost bone of the index finger": [ + "HP:0009505" + ], + "fragmentation of the epiphysis of the distal phalanx of the 2nd finger": [ + "HP:0009506" + ], + "fragmentation of end part of the outermost bone of the index finger": [ + "HP:0009506" + ], + "irregular epiphysis of the distal phalanx of the 2nd finger": [ + "HP:0009507" + ], + "irregular end part of the outermost bone of the index finger": [ + "HP:0009507" + ], + "ivory epiphysis of the distal phalanx of the 2nd finger": [ + "HP:0009508" + ], + "increase bone density of end part of the outermost bone of the index finger": [ + "HP:0009508" + ], + "increased bone density of end part of the outermost bone of the index finger": [ + "HP:0009508" + ], + "ivory epiphysis of terminal index finger phalanx": [ + "HP:0009508" + ], + "pseudoepiphysis of the distal phalanx of the 2nd finger": [ + "HP:0009509" + ], + "small epiphysis of the distal phalanx of the 2nd finger": [ + "HP:0009510" + ], + "small end part of the outermost bone of the index finger": [ + "HP:0009510" + ], + "stippling of the epiphysis of the distal phalanx of the 2nd finger": [ + "HP:0009511" + ], + "speckled calcification in end part of the outermost bone of the index finger": [ + "HP:0009511" + ], + "speckled calcifications in end part of the outermost bone of the index finger": [ + "HP:0009511" + ], + "triangular epiphysis of the distal phalanx of the 2nd finger": [ + "HP:0009512" + ], + "triangular end part of the outermost bone of the index finger": [ + "HP:0009512" + ], + "absent epiphysis of the middle phalanx of the 2nd finger": [ + "HP:0009513" + ], + "absent epiphysis of middle phalanx of index finger": [ + "HP:0009513" + ], + "absent epiphyses of middle phalanx of index finger": [ + "HP:0009513" + ], + "miss end part of the middle long bone of the index finger": [ + "HP:0009513" + ], + "missing end part of the middle long bone of the index finger": [ + "HP:0009513" + ], + "bracket epiphysis of the middle phalanx of the 2nd finger": [ + "HP:0009514" + ], + "bracket shape end part of the middle long bone of the index finger": [ + "HP:0009514" + ], + "bracket shaped end part of the middle long bone of the index finger": [ + "HP:0009514" + ], + "cone - shaped epiphysis of the middle phalanx of the 2nd finger": [ + "HP:0009515" + ], + "cone - shaped end part of the middle long bone of the index finger": [ + "HP:0009515" + ], + "cone - shaped epiphysis of middle phalanx of index finger": [ + "HP:0009515" + ], + "cone - shaped epiphyses of middle phalanx of index finger": [ + "HP:0009515" + ], + "enlarged epiphysis of the middle phalanx of the 2nd finger": [ + "HP:0009516" + ], + "enlarged end part of the middle bone of the index finger": [ + "HP:0009516" + ], + "fragmentation of the epiphysis of the middle phalanx of the 2nd finger": [ + "HP:0009517" + ], + "fragmentation of end part of the middle long bone of the index finger": [ + "HP:0009517" + ], + "irregular epiphysis of the middle phalanx of the 2nd finger": [ + "HP:0009518" + ], + "irregular end part of the middle long bone of the index finger": [ + "HP:0009518" + ], + "ivory epiphysis of the middle phalanx of the 2nd finger": [ + "HP:0009519" + ], + "increase bone density of end part of the middle bone of the index finger": [ + "HP:0009519" + ], + "increased bone density of end part of the middle bone of the index finger": [ + "HP:0009519" + ], + "pseudoepiphysis of the middle phalanx of the 2nd finger": [ + "HP:0009520" + ], + "small epiphysis of the middle phalanx of the 2nd finger": [ + "HP:0009521" + ], + "small end part of the innermost long bone of index finger": [ + "HP:0009521" + ], + "stippling of the epiphysis of the middle phalanx of the 2nd finger": [ + "HP:0009522" + ], + "speckled calcification in end part of the middle bone of the index finger": [ + "HP:0009522" + ], + "speckled calcifications in end part of the middle bone of the index finger": [ + "HP:0009522" + ], + "triangular epiphysis of the middle phalanx of the 2nd finger": [ + "HP:0009523" + ], + "triangular end part of the middle bone of the index finger": [ + "HP:0009523" + ], + "absent epiphysis of the proximal phalanx of the 2nd finger": [ + "HP:0009524" + ], + "absent end part of innermost long bone of index finger": [ + "HP:0009524" + ], + "bracket epiphysis of the proximal phalanx of the 2nd finger": [ + "HP:0009525" + ], + "bracket epiphysis of proximal index finger phalanx": [ + "HP:0009525" + ], + "bracket epiphyses of proximal index finger phalanx": [ + "HP:0009525" + ], + "bracket shape end part of innermost long bone of index finger": [ + "HP:0009525" + ], + "bracket shaped end part of innermost long bone of index finger": [ + "HP:0009525" + ], + "cone - shaped epiphysis of the proximal phalanx of the 2nd finger": [ + "HP:0009526" + ], + "cone - shaped end part of innermost long bone of index finger": [ + "HP:0009526" + ], + "cone - shaped epiphysis of proximal index finger phalanx": [ + "HP:0009526" + ], + "enlarged epiphysis of the proximal phalanx of the 2nd finger": [ + "HP:0009527" + ], + "enlarged end part of innermost long bone of index finger": [ + "HP:0009527" + ], + "large epiphysis of proximal index finger phalanx": [ + "HP:0009527" + ], + "fragmentation of the epiphysis of the proximal phalanx of the 2nd finger": [ + "HP:0009528" + ], + "fragmentation of end part of innermost long bone of index finger": [ + "HP:0009528" + ], + "irregular epiphysis of the proximal phalanx of the 2nd finger": [ + "HP:0009529" + ], + "irregular end part of innermost long bone of index finger": [ + "HP:0009529" + ], + "ivory epiphysis of the proximal phalanx of the 2nd finger": [ + "HP:0009530" + ], + "increase bone density of end part of the innermost bone of the index finger": [ + "HP:0009530" + ], + "increased bone density of end part of the innermost bone of the index finger": [ + "HP:0009530" + ], + "pseudoepiphysis of the proximal phalanx of the 2nd finger": [ + "HP:0009531" + ], + "small epiphysis of the proximal phalanx of the 2nd finger": [ + "HP:0009532" + ], + "small end part of proximal long bond of index finger": [ + "HP:0009532" + ], + "stippling of the epiphysis of the proximal phalanx of the 2nd finger": [ + "HP:0009533" + ], + "speckled calcification in end part of the innermost long bone of index finger": [ + "HP:0009533" + ], + "speckled calcifications in end part of the innermost long bone of index finger": [ + "HP:0009533" + ], + "triangular epiphysis of the proximal phalanx of the 2nd finger": [ + "HP:0009534" + ], + "triangular end part of innermost long bone of index finger": [ + "HP:0009534" + ], + "triangular epiphysis of proximal index finger phalanx": [ + "HP:0009534" + ], + "aplasia of the 2nd finger": [ + "HP:0009535" + ], + "absent index finger": [ + "HP:0009535" + ], + "absent index finger phalanx": [ + "HP:0009535" + ], + "absent index finger phalanges": [ + "HP:0009535" + ], + "aplasia of the index finger": [ + "HP:0009535" + ], + "short 2nd finger": [ + "HP:0009536" + ], + "hypoplastic index finger phalanx": [ + "HP:0009536" + ], + "hypoplastic index finger phalanges": [ + "HP:0009536" + ], + "hypoplastic / small index finger": [ + "HP:0009536" + ], + "short index finger": [ + "HP:0009536" + ], + "short index finger phalanx": [ + "HP:0009536" + ], + "short index finger phalanges": [ + "HP:0009536" + ], + "short index fingers": [ + "HP:0009536" + ], + "flexion contracture of the 2nd finger": [ + "HP:0009537" + ], + "joint contracture of the 2nd finger": [ + "HP:0009537" + ], + "joint contractures of the 2nd finger": [ + "HP:0009537" + ], + "contracture of the distal interphalangeal joint of the 2nd finger": [ + "HP:0009538" + ], + "contracture of the metacarpophalangeal joint of the 2nd finger": [ + "HP:0009539" + ], + "contracture of the proximal interphalangeal joint of the 2nd finger": [ + "HP:0009540" + ], + "camptodactyly of 2nd finger": [ + "HP:0009540" + ], + "camptodactyly of index finger": [ + "HP:0009540" + ], + "camptodactyly of second finger": [ + "HP:0009540" + ], + "abnormality of the phalanx of the 2nd finger": [ + "HP:0009541" + ], + "abnormality of the phalanges of the 2nd finger": [ + "HP:0009541" + ], + "abnormal index finger bone": [ + "HP:0009541" + ], + "abnormal index finger bones": [ + "HP:0009541" + ], + "abnormality of 2nd finger phalanx": [ + "HP:0009541" + ], + "abnormality of 2nd finger phalanges": [ + "HP:0009541" + ], + "abnormality of the distal phalanx of the 2nd finger": [ + "HP:0009542" + ], + "abnormality of terminal index finger phalanx": [ + "HP:0009542" + ], + "abnormality of the outermost bone of the 2nd finger": [ + "HP:0009542" + ], + "abnormality of the middle phalanx of the 2nd finger": [ + "HP:0009543" + ], + "abnormal middle index finger bone": [ + "HP:0009543" + ], + "abnormality of middle 2nd finger phalanx": [ + "HP:0009543" + ], + "abnormality of the proximal phalanx of the 2nd finger": [ + "HP:0009544" + ], + "abnormal innermost index finger bone": [ + "HP:0009544" + ], + "abnormality of the proximal 2nd finger phalanx": [ + "HP:0009544" + ], + "symphalangism of the 2nd finger": [ + "HP:0009545" + ], + "fuse index finger bone": [ + "HP:0009545" + ], + "fused index finger bones": [ + "HP:0009545" + ], + "symphalangism of index finger phalanx": [ + "HP:0009545" + ], + "symphalangism of index finger phalanges": [ + "HP:0009545" + ], + "triangular shape phalanx of the 2nd finger": [ + "HP:0009546" + ], + "triangular shaped phalanges of the 2nd finger": [ + "HP:0009546" + ], + "triangular bone of index finger": [ + "HP:0009546" + ], + "triangular bones of index finger": [ + "HP:0009546" + ], + "triangular index finger phalanx": [ + "HP:0009546" + ], + "triangular index finger phalanges": [ + "HP:0009546" + ], + "broad phalanx of the 2nd finger": [ + "HP:0009547" + ], + "broad phalanges of the 2nd finger": [ + "HP:0009547" + ], + "wide index finger bone": [ + "HP:0009547" + ], + "wide index finger bones": [ + "HP:0009547" + ], + "wide / broad index finger phalanx": [ + "HP:0009547" + ], + "wide / broad index finger phalanges": [ + "HP:0009547" + ], + "bullet - shaped phalanx of the 2nd finger": [ + "HP:0009548" + ], + "bullet - shaped phalanges of the 2nd finger": [ + "HP:0009548" + ], + "bullet - shaped index finger bone": [ + "HP:0009548" + ], + "bullet - shaped index finger bones": [ + "HP:0009548" + ], + "curve phalanx of the 2nd finger": [ + "HP:0009549" + ], + "curved phalanges of the 2nd finger": [ + "HP:0009549" + ], + "curve index finger bone": [ + "HP:0009549" + ], + "curved index finger bones": [ + "HP:0009549" + ], + "osteolytic defect of the phalanx of the 2nd finger": [ + "HP:0009550" + ], + "osteolytic defects of the phalanges of the 2nd finger": [ + "HP:0009550" + ], + "lytic defect in index finger phalanx": [ + "HP:0009550" + ], + "lytic defect in index finger phalanges": [ + "HP:0009550" + ], + "patchy sclerosis of 2nd finger phalanx": [ + "HP:0009551" + ], + "patchy sclerosis of the phalanx of the 2nd finger": [ + "HP:0009551" + ], + "patchy sclerosis of the phalanges of the 2nd finger": [ + "HP:0009551" + ], + "uneven increase in bone density in index finger bone": [ + "HP:0009551" + ], + "aplasia / hypoplasia of the phalanx of the 2nd finger": [ + "HP:0009552" + ], + "aplasia / hypoplasia of the phalanges of the 2nd finger": [ + "HP:0009552" + ], + "absent / small index finger bone": [ + "HP:0009552" + ], + "absent / underdevelop index finger bone": [ + "HP:0009552" + ], + "absent / underdeveloped index finger bone": [ + "HP:0009552" + ], + "abnormality of the hairline": [ + "HP:0009553" + ], + "preauricular hair displacement": [ + "HP:0009554" + ], + "hair displacement , preauricular , towards lateral cheekbone": [ + "HP:0009554" + ], + "hair grow down to cheek": [ + "HP:0009554" + ], + "hair growing down to cheek": [ + "HP:0009554" + ], + "projection of scalp hair onto lateral cheek": [ + "HP:0009554" + ], + "hypoplasia of the pharynx": [ + "HP:0009555" + ], + "decrease diameter of pharynx": [ + "HP:0009555" + ], + "decreased diameter of pharynx": [ + "HP:0009555" + ], + "decreased length of pharynx": [ + "HP:0009555" + ], + "decreased size of pharynx": [ + "HP:0009555" + ], + "decreased volume of pharynx": [ + "HP:0009555" + ], + "decrease width of pharynx": [ + "HP:0009555" + ], + "decreased width of pharynx": [ + "HP:0009555" + ], + "hypotrophic pharynx": [ + "HP:0009555" + ], + "small pharynx": [ + "HP:0009555" + ], + "underdevelopment of pharynx": [ + "HP:0009555" + ], + "absent tibia": [ + "HP:0009556" + ], + "absent shankbone": [ + "HP:0009556" + ], + "absent shinbone": [ + "HP:0009556" + ], + "aplasia of the tibia": [ + "HP:0009556" + ], + "aplasia / hypoplasia of the distal phalanx of the 2nd finger": [ + "HP:0009557" + ], + "absent / small outermost index finger bone": [ + "HP:0009557" + ], + "absent / underdevelop outermost index finger bone": [ + "HP:0009557" + ], + "absent / underdeveloped outermost index finger bone": [ + "HP:0009557" + ], + "broad distal phalanx of the 2nd finger": [ + "HP:0009558" + ], + "wide outermost bone of the index finger": [ + "HP:0009558" + ], + "bullet - shaped distal phalanx of the 2nd finger": [ + "HP:0009559" + ], + "bullet - shape outermost bone of the index finger": [ + "HP:0009559" + ], + "bullet - shaped outermost bone of the index finger": [ + "HP:0009559" + ], + "curve distal phalanx of the 2nd finger": [ + "HP:0009560" + ], + "curved distal phalanx of the 2nd finger": [ + "HP:0009560" + ], + "curve outermost bone of the index finger": [ + "HP:0009560" + ], + "curved outermost bone of the index finger": [ + "HP:0009560" + ], + "osteolytic defect of the distal phalanx of the 2nd finger": [ + "HP:0009561" + ], + "osteolytic defects of the distal phalanx of the 2nd finger": [ + "HP:0009561" + ], + "acro - osteolysis of index finger": [ + "HP:0009561" + ], + "acro - osteolysis of terminal index finger phalanx": [ + "HP:0009561" + ], + "osteolytic defect of the outermost bone of the 2nd finger": [ + "HP:0009561" + ], + "osteolytic defects of the outermost bone of the 2nd finger": [ + "HP:0009561" + ], + "patchy sclerosis of the distal phalanx of the 2nd finger": [ + "HP:0009562" + ], + "uneven increase in bone density in the outermost bone of the 2nd finger": [ + "HP:0009562" + ], + "distal / middle symphalangism of 2nd finger": [ + "HP:0009563" + ], + "fuse outermost and middle index finger bone": [ + "HP:0009563" + ], + "fused outermost and middle index finger bones": [ + "HP:0009563" + ], + "symphalangism of the distal and middle phalanx of the 2nd finger": [ + "HP:0009563" + ], + "symphalangism of the distal and middle phalanges of the 2nd finger": [ + "HP:0009563" + ], + "triangular shape distal phalanx of the 2nd finger": [ + "HP:0009564" + ], + "triangular shaped distal phalanx of the 2nd finger": [ + "HP:0009564" + ], + "triangular shape outermost bone of the 2nd finger": [ + "HP:0009564" + ], + "triangular shaped outermost bone of the 2nd finger": [ + "HP:0009564" + ], + "aplasia of the distal phalanx of the 2nd finger": [ + "HP:0009565" + ], + "absent outermost index finger bone": [ + "HP:0009565" + ], + "absent terminal index finger phalanx": [ + "HP:0009565" + ], + "short distal phalanx of the 2nd finger": [ + "HP:0009566" + ], + "hypoplastic terminal index finger phalanx": [ + "HP:0009566" + ], + "hypoplastic / small distal phalanx of the 2nd finger": [ + "HP:0009566" + ], + "short distal phalanx of the second finger": [ + "HP:0009566" + ], + "short outermost bone of the index finger": [ + "HP:0009566" + ], + "short terminal index finger phalanx": [ + "HP:0009566" + ], + "aplasia / hypoplasia of the middle phalanx of the 2nd finger": [ + "HP:0009568" + ], + "absent / hypoplastic middle phalanx of 2nd finger": [ + "HP:0009568" + ], + "absent / small middle index finger bone": [ + "HP:0009568" + ], + "absent / underdevelop middle index finger bone": [ + "HP:0009568" + ], + "absent / underdeveloped middle index finger bone": [ + "HP:0009568" + ], + "hypoplastic / aplastic middle phalanx of index finger": [ + "HP:0009568" + ], + "broad middle phalanx of the 2nd finger": [ + "HP:0009569" + ], + "broad middle bone of the index finger": [ + "HP:0009569" + ], + "bullet - shape middle phalanx of the 2nd finger": [ + "HP:0009570" + ], + "bullet - shaped middle phalanx of the 2nd finger": [ + "HP:0009570" + ], + "bullet - shape middle bone of index finger": [ + "HP:0009570" + ], + "bullet - shaped middle bone of index finger": [ + "HP:0009570" + ], + "curve middle phalanx of the 2nd finger": [ + "HP:0009571" + ], + "curved middle phalanx of the 2nd finger": [ + "HP:0009571" + ], + "curve middle bone of the index finger": [ + "HP:0009571" + ], + "curved middle bone of the index finger": [ + "HP:0009571" + ], + "osteolytic defect of the middle phalanx of the 2nd finger": [ + "HP:0009572" + ], + "osteolytic defects of the middle phalanx of the 2nd finger": [ + "HP:0009572" + ], + "lytic defect of middle index finger phalanx": [ + "HP:0009572" + ], + "lytic defects of middle index finger phalanx": [ + "HP:0009572" + ], + "patchy sclerosis of the middle phalanx of the 2nd finger": [ + "HP:0009573" + ], + "uneven increase in bone density in the middle bone of the index finger": [ + "HP:0009573" + ], + "symphalangism of middle phalanx of 2nd finger": [ + "HP:0009574" + ], + "fuse middle bone of index finger": [ + "HP:0009574" + ], + "fused middle bone of index finger": [ + "HP:0009574" + ], + "triangular shape middle phalanx of the 2nd finger": [ + "HP:0009575" + ], + "triangular shaped middle phalanx of the 2nd finger": [ + "HP:0009575" + ], + "triangular shape middle bone of index finger": [ + "HP:0009575" + ], + "triangular shaped middle bone of index finger": [ + "HP:0009575" + ], + "absent middle phalanx of 2nd finger": [ + "HP:0009576" + ], + "absent middle bone of index finger": [ + "HP:0009576" + ], + "absent middle phalanx of index finger": [ + "HP:0009576" + ], + "aplasia of the middle phalanx of the 2nd finger": [ + "HP:0009576" + ], + "short middle phalanx of the 2nd finger": [ + "HP:0009577" + ], + "brachymesophalangy ii ( finger )": [ + "HP:0009577" + ], + "hypoplastic middle index finger phalanx": [ + "HP:0009577" + ], + "hypoplastic / small middle phalanx of the 2nd finger": [ + "HP:0009577" + ], + "short middle bone of index finger": [ + "HP:0009577" + ], + "proximal / middle symphalangism of the 2nd finger": [ + "HP:0009579" + ], + "fuse innermost and middle index finger bone": [ + "HP:0009579" + ], + "fused innermost and middle index finger bones": [ + "HP:0009579" + ], + "aplasia / hypoplasia of the proximal phalanx of the 2nd finger": [ + "HP:0009580" + ], + "absent / small innermost index finger bone": [ + "HP:0009580" + ], + "absent / underdevelop innermost index finger bone": [ + "HP:0009580" + ], + "absent / underdeveloped innermost index finger bone": [ + "HP:0009580" + ], + "broad proximal phalanx of the 2nd finger": [ + "HP:0009581" + ], + "wide innermost bone of index finger": [ + "HP:0009581" + ], + "wide / broad proximal index finger phalanx": [ + "HP:0009581" + ], + "bullet - shape proximal phalanx of the 2nd finger": [ + "HP:0009582" + ], + "bullet - shaped proximal phalanx of the 2nd finger": [ + "HP:0009582" + ], + "bullet - shape innermost bone of index finger": [ + "HP:0009582" + ], + "bullet - shaped innermost bone of index finger": [ + "HP:0009582" + ], + "curve proximal phalanx of the 2nd finger": [ + "HP:0009583" + ], + "curved proximal phalanx of the 2nd finger": [ + "HP:0009583" + ], + "curve innermost bone of index finger": [ + "HP:0009583" + ], + "curved innermost bone of index finger": [ + "HP:0009583" + ], + "osteolytic defect of the proximal phalanx of the 2nd finger": [ + "HP:0009584" + ], + "osteolytic defects of the proximal phalanx of the 2nd finger": [ + "HP:0009584" + ], + "lytic defect of proximal index finger phalanx": [ + "HP:0009584" + ], + "lytic defects of proximal index finger phalanx": [ + "HP:0009584" + ], + "patchy sclerosis of the proximal phalanx of the 2nd finger": [ + "HP:0009585" + ], + "uneven increase in bone density in innermost index finger bone": [ + "HP:0009585" + ], + "symphalangism affect the proximal phalanx of the 2nd finger": [ + "HP:0009586" + ], + "symphalangism affecting the proximal phalanx of the 2nd finger": [ + "HP:0009586" + ], + "fuse innermost bone of index finger": [ + "HP:0009586" + ], + "fused innermost bone of index finger": [ + "HP:0009586" + ], + "triangular shape proximal phalanx of the 2nd finger": [ + "HP:0009587" + ], + "triangular shaped proximal phalanx of the 2nd finger": [ + "HP:0009587" + ], + "triangular proximal index finger phalanx": [ + "HP:0009587" + ], + "triangular shape innermost bone of index finger": [ + "HP:0009587" + ], + "triangular shaped innermost bone of index finger": [ + "HP:0009587" + ], + "vestibular schwannoma": [ + "HP:0009588" + ], + "acoustic neuroma": [ + "HP:0009588" + ], + "vestibular neurilemmoma": [ + "HP:0009588" + ], + "vestibular neurinoma": [ + "HP:0009588" + ], + "vestibular neurolemmoma": [ + "HP:0009588" + ], + "vestibular schwann cell tumor": [ + "HP:0009588" + ], + "vestibular schwann cell tumour": [ + "HP:0009588" + ], + "bilateral vestibular schwannoma": [ + "HP:0009589" + ], + "bilateral acoustic neuroma": [ + "HP:0009589" + ], + "bilateral acoustic neuromas": [ + "HP:0009589" + ], + "unilateral vestibular schwannoma": [ + "HP:0009590" + ], + "abnormality of the vestibulocochlear nerve": [ + "HP:0009591" + ], + "abnormality of the eighth cranial nerve": [ + "HP:0009591" + ], + "abnormality of the viiith cranial nerve": [ + "HP:0009591" + ], + "astrocytoma": [ + "HP:0009592" + ], + "peripheral schwannoma": [ + "HP:0009593" + ], + "retinal hamartoma": [ + "HP:0009594" + ], + "occasional neurofibroma": [ + "HP:0009595" + ], + "occasional neurofibromas": [ + "HP:0009595" + ], + "aplasia of the proximal phalanx of the 2nd finger": [ + "HP:0009596" + ], + "absent innermost bone of index finger": [ + "HP:0009596" + ], + "short proximal phalanx of the 2nd finger": [ + "HP:0009597" + ], + "hypoplastic / small proximal phalanx of the 2nd finger": [ + "HP:0009597" + ], + "short proximal index finger phalanx": [ + "HP:0009597" + ], + "short proximal phalanx of the second finger": [ + "HP:0009597" + ], + "symphalangism of the proximal phalanx of the 2nd finger with the 2nd metacarpal": [ + "HP:0009598" + ], + "fuse innermost bone of index finger with 2nd long bone of hand": [ + "HP:0009598" + ], + "fused innermost bone of index finger with 2nd long bone of hand": [ + "HP:0009598" + ], + "abnormality of thumb epiphysis": [ + "HP:0009599" + ], + "abnormality of end part of thumb long bone": [ + "HP:0009599" + ], + "abnormality of the epiphysis of the thumb": [ + "HP:0009599" + ], + "abnormality of the epiphyses of the thumb": [ + "HP:0009599" + ], + "abnormality of thumb epiphyses": [ + "HP:0009599" + ], + "flexion contracture of thumb": [ + "HP:0009600" + ], + "contracture of thumb": [ + "HP:0009600" + ], + "flexion deformity of thumb": [ + "HP:0009600" + ], + "flexion deformities of thumbs": [ + "HP:0009600" + ], + "joint contracture of the thumb": [ + "HP:0009600" + ], + "joint contractures of the thumb": [ + "HP:0009600" + ], + "aplasia / hypoplasia of the thumb": [ + "HP:0009601" + ], + "absent or hypoplastic thumb": [ + "HP:0009601" + ], + "absent or hypoplastic thumbs": [ + "HP:0009601" + ], + "absent / hypoplastic thumb": [ + "HP:0009601" + ], + "absent / hypoplastic thumbs": [ + "HP:0009601" + ], + "absent / small thumb": [ + "HP:0009601" + ], + "absent / underdevelop thumb": [ + "HP:0009601" + ], + "absent / underdeveloped thumb": [ + "HP:0009601" + ], + "aplasia / hypoplasia of thumb": [ + "HP:0009601" + ], + "aplasia / hypoplasia of thumbs": [ + "HP:0009601" + ], + "aplastic / hypoplastic thumb": [ + "HP:0009601" + ], + "aplastic / hypoplastic thumbs": [ + "HP:0009601" + ], + "hypoplastic to aplastic thumb": [ + "HP:0009601" + ], + "hypoplastic to aplastic thumbs": [ + "HP:0009601" + ], + "hypoplastic / absent thumb": [ + "HP:0009601" + ], + "thumb aplasia / hypoplasia": [ + "HP:0009601" + ], + "abnormality of thumb phalanx": [ + "HP:0009602" + ], + "abnormality of the thumb bone": [ + "HP:0009602" + ], + "abnormality of the thumb bones": [ + "HP:0009602" + ], + "abnormality of thumb phalanges": [ + "HP:0009602" + ], + "deviation of the thumb": [ + "HP:0009603" + ], + "abnormal thumb placement": [ + "HP:0009603" + ], + "deviate thumb": [ + "HP:0009603" + ], + "deviated thumb": [ + "HP:0009603" + ], + "displacement of the thumb": [ + "HP:0009603" + ], + "complete duplication of distal phalanx of the thumb": [ + "HP:0009606" + ], + "complete duplication of outermost bone of the thumb": [ + "HP:0009606" + ], + "complete duplication of proximal phalanx of the thumb": [ + "HP:0009608" + ], + "complete duplication of the innermost bone of the thumb": [ + "HP:0009608" + ], + "duplication of the 1st metacarpal": [ + "HP:0009609" + ], + "partial / complete duplication of the 1st long bone of hand": [ + "HP:0009609" + ], + "partial / complete duplication of the 1st metacarpal": [ + "HP:0009609" + ], + "bifid distal phalanx of the thumb": [ + "HP:0009611" + ], + "bifid distal phalanx of thumb": [ + "HP:0009611" + ], + "bifid terminal phalanx of thumb": [ + "HP:0009611" + ], + "bifid terminal phalanges of thumbs": [ + "HP:0009611" + ], + "bifid thumb distal phalanx": [ + "HP:0009611" + ], + "incipient distal thumb phalanx duplication": [ + "HP:0009611" + ], + "notch outermost bone of the thumb": [ + "HP:0009611" + ], + "notched outermost bone of the thumb": [ + "HP:0009611" + ], + "notch outermost bone of thumb": [ + "HP:0009611" + ], + "notched outermost bone of thumb": [ + "HP:0009611" + ], + "notched terminal thumb phalanx": [ + "HP:0009611" + ], + "duplication of the distal phalanx of the thumb": [ + "HP:0009612" + ], + "double thumb distal phalanx": [ + "HP:0009612" + ], + "double thumb distal phalanges": [ + "HP:0009612" + ], + "duplicate terminal phalanx of thumb": [ + "HP:0009612" + ], + "duplicated terminal phalanx of thumb": [ + "HP:0009612" + ], + "duplication of distal thumb phalanx": [ + "HP:0009612" + ], + "duplication of terminal thumb phalanx": [ + "HP:0009612" + ], + "duplication of the outermost bone of the thumb": [ + "HP:0009612" + ], + "partial / complete duplication of the distal phalanx of the thumb": [ + "HP:0009612" + ], + "duplication of the proximal phalanx of the thumb": [ + "HP:0009613" + ], + "notch innermost bone of thumb": [ + "HP:0009613" + ], + "notched innermost bone of thumb": [ + "HP:0009613" + ], + "partial / complete duplication of the proximal phalanx of the thumb": [ + "HP:0009613" + ], + "bifid proximal phalanx of the thumb": [ + "HP:0009614" + ], + "notch thumb bone": [ + "HP:0009614" + ], + "notched thumb bone": [ + "HP:0009614" + ], + "complete duplication of the first metacarpal": [ + "HP:0009615" + ], + "complete duplication of the first long bone of hand": [ + "HP:0009615" + ], + "bifid first metacarpal": [ + "HP:0009616" + ], + "notch first long bone of hand": [ + "HP:0009616" + ], + "notched first long bone of hand": [ + "HP:0009616" + ], + "partial duplication of the first metacarpal": [ + "HP:0009616" + ], + "abnormality of the distal phalanx of the thumb": [ + "HP:0009617" + ], + "abnormality of terminal thumb phalanx": [ + "HP:0009617" + ], + "abnormality of the outermost bone of the thumb": [ + "HP:0009617" + ], + "abnormality of the proximal phalanx of the thumb": [ + "HP:0009618" + ], + "abnormal innermost thumb bone": [ + "HP:0009618" + ], + "abnormality of proximal thumb phalanx": [ + "HP:0009618" + ], + "obsolete radial deviation of the thumb": [ + "HP:0009620" + ], + "obsolete ulnar deviation of the thumb": [ + "HP:0009621" + ], + "distally place thumb": [ + "HP:0009622" + ], + "distally placed thumb": [ + "HP:0009622" + ], + "proximal placement of thumb": [ + "HP:0009623" + ], + "attachment of thumb close to wrist": [ + "HP:0009623" + ], + "low implantation of the thumb": [ + "HP:0009623" + ], + "low - set thumb": [ + "HP:0009623" + ], + "proximally place thumb": [ + "HP:0009623" + ], + "proximally placed thumbs": [ + "HP:0009623" + ], + "contracture of the carpometacarpal joint of the thumb": [ + "HP:0009624" + ], + "contractures of the carpometacarpal joint of the thumb": [ + "HP:0009624" + ], + "contracture of the metacarpophalangeal joint of the thumb": [ + "HP:0009625" + ], + "contractures of the metacarpophalangeal joint of the thumb": [ + "HP:0009625" + ], + "contracture of the interphalangeal joint of the thumb": [ + "HP:0009626" + ], + "contractures of the interphalangeal joint of the thumb": [ + "HP:0009626" + ], + "interphalangeal extension contracture of thumb": [ + "HP:0009626" + ], + "interphalangeal extension contractures of thumbs": [ + "HP:0009626" + ], + "aplasia / hypoplasia of the proximal phalanx of the thumb": [ + "HP:0009629" + ], + "absent / small innermost thumb bone": [ + "HP:0009629" + ], + "absent / underdevelop innermost thumb bone": [ + "HP:0009629" + ], + "absent / underdeveloped innermost thumb bone": [ + "HP:0009629" + ], + "broad proximal phalanx of the thumb": [ + "HP:0009630" + ], + "broad innermost thumb bone": [ + "HP:0009630" + ], + "bullet - shape proximal phalanx of the thumb": [ + "HP:0009631" + ], + "bullet - shaped proximal phalanx of the thumb": [ + "HP:0009631" + ], + "bullet - shape innermost thumb bone": [ + "HP:0009631" + ], + "bullet - shaped innermost thumb bone": [ + "HP:0009631" + ], + "curve proximal phalanx of the thumb": [ + "HP:0009632" + ], + "curved proximal phalanx of the thumb": [ + "HP:0009632" + ], + "curve innermost thumb bone": [ + "HP:0009632" + ], + "curved innermost thumb bone": [ + "HP:0009632" + ], + "osteolytic defect of the proximal phalanx of the thumb": [ + "HP:0009633" + ], + "osteolytic defects of the proximal phalanx of the thumb": [ + "HP:0009633" + ], + "patchy sclerosis of the proximal phalanx of the thumb": [ + "HP:0009634" + ], + "uneven increase in bone density in the innermost thumb bone": [ + "HP:0009634" + ], + "synostosis of thumb phalanx": [ + "HP:0009635" + ], + "fusion of thumb bone": [ + "HP:0009635" + ], + "triangular shape proximal phalanx of the thumb": [ + "HP:0009636" + ], + "triangular shaped proximal phalanx of the thumb": [ + "HP:0009636" + ], + "triangular innermost thumb bone": [ + "HP:0009636" + ], + "triangular proximal thumb phalanx": [ + "HP:0009636" + ], + "absent proximal phalanx of thumb": [ + "HP:0009637" + ], + "absent innermost thumb bone": [ + "HP:0009637" + ], + "absent ossification / absent proximal thumb phalanx": [ + "HP:0009637" + ], + "aplasia of the proximal phalanx of the thumb": [ + "HP:0009637" + ], + "short proximal phalanx of thumb": [ + "HP:0009638" + ], + "hypoplastic / small proximal phalanx of the thumb": [ + "HP:0009638" + ], + "short proximal phalanges of thumb": [ + "HP:0009638" + ], + "short proximal thumb bone": [ + "HP:0009638" + ], + "short proximal thumb phalanx": [ + "HP:0009638" + ], + "synostosis of the proximal phalanx of the thumb with the 1st metacarpal": [ + "HP:0009640" + ], + "ankylosis of the metacarpophalangeal joint of the thumb": [ + "HP:0009640" + ], + "fusion of the innermost bone of the thumb with the 1st long bone of hand": [ + "HP:0009640" + ], + "aplasia / hypoplasia of the distal phalanx of the thumb": [ + "HP:0009641" + ], + "absent / small outermost thumb bone": [ + "HP:0009641" + ], + "absent / underdevelop outermost thumb bone": [ + "HP:0009641" + ], + "absent / underdeveloped outermost thumb bone": [ + "HP:0009641" + ], + "broad distal phalanx of the thumb": [ + "HP:0009642" + ], + "broad outermost bone of the thumb": [ + "HP:0009642" + ], + "broad terminal thumb phalanx": [ + "HP:0009642" + ], + "wide distal phalanx of thumb": [ + "HP:0009642" + ], + "wide outermost bone of thumb": [ + "HP:0009642" + ], + "bullet - shaped distal phalanx of the thumb": [ + "HP:0009643" + ], + "bullet - shape outermost bone of the thumb": [ + "HP:0009643" + ], + "bullet - shaped outermost bone of the thumb": [ + "HP:0009643" + ], + "curve distal phalanx of the thumb": [ + "HP:0009644" + ], + "curved distal phalanx of the thumb": [ + "HP:0009644" + ], + "curve outermost bone of the thumb": [ + "HP:0009644" + ], + "curved outermost bone of the thumb": [ + "HP:0009644" + ], + "osteolytic defect of the distal phalanx of the thumb": [ + "HP:0009645" + ], + "osteolytic defects of the distal phalanx of the thumb": [ + "HP:0009645" + ], + "osteolytic defect of the outermost bone of the thumb": [ + "HP:0009645" + ], + "osteolytic defects of the outermost bone of the thumb": [ + "HP:0009645" + ], + "patchy sclerosis of the distal phalanx of the thumb": [ + "HP:0009646" + ], + "uneven increase in bone density in the outermost bone of the thumb": [ + "HP:0009646" + ], + "triangular shape distal phalanx of the thumb": [ + "HP:0009648" + ], + "triangular shaped distal phalanx of the thumb": [ + "HP:0009648" + ], + "triangular shape outermost bone of the thumb": [ + "HP:0009648" + ], + "triangular shaped outermost bone of the thumb": [ + "HP:0009648" + ], + "aplasia of the distal phalanx of the thumb": [ + "HP:0009649" + ], + "absence of the outermost bone of the thumb": [ + "HP:0009649" + ], + "absent ossification / absent terminal thumb phalanx": [ + "HP:0009649" + ], + "aplasia of the outermost bone of the thumb": [ + "HP:0009649" + ], + "short distal phalanx of the thumb": [ + "HP:0009650" + ], + "hypoplastic terminal thumb phalanx": [ + "HP:0009650" + ], + "hypoplastic / small distal phalanx of the thumb": [ + "HP:0009650" + ], + "short outermost bone of the thumb": [ + "HP:0009650" + ], + "short terminal thumb phalanx": [ + "HP:0009650" + ], + "short thumb terminal phalanx": [ + "HP:0009650" + ], + "small terminal thumb phalanx": [ + "HP:0009650" + ], + "bullet - shaped thumb phalanx": [ + "HP:0009652" + ], + "bullet - shaped phalanx of the thumb": [ + "HP:0009652" + ], + "bullet - shaped phalanges of the thumb": [ + "HP:0009652" + ], + "bullet - shaped thumb bone": [ + "HP:0009652" + ], + "curve thumb phalanx": [ + "HP:0009653" + ], + "curved thumb phalanx": [ + "HP:0009653" + ], + "curve phalanx of the thumb": [ + "HP:0009653" + ], + "curved phalanges of the thumb": [ + "HP:0009653" + ], + "curve thumb bone": [ + "HP:0009653" + ], + "curved thumb bone": [ + "HP:0009653" + ], + "osteolytic defect of thumb phalanx": [ + "HP:0009654" + ], + "osteolytic defect of the phalanx of the thumb": [ + "HP:0009654" + ], + "osteolytic defects of the phalanges of the thumb": [ + "HP:0009654" + ], + "patchy sclerosis of thumb phalanx": [ + "HP:0009655" + ], + "patchy sclerosis of the phalanx of the thumb": [ + "HP:0009655" + ], + "patchy sclerosis of the phalanges of the thumb": [ + "HP:0009655" + ], + "uneven increase in bone density in thumb bone": [ + "HP:0009655" + ], + "symphalangism of the thumb": [ + "HP:0009656" + ], + "fuse thumb bone": [ + "HP:0009656" + ], + "fused thumb bones": [ + "HP:0009656" + ], + "fuse thumb phalanx": [ + "HP:0009656" + ], + "fused thumb phalanges": [ + "HP:0009656" + ], + "symphalangism of the distal and proximal phalanx of the thumb": [ + "HP:0009656" + ], + "symphalangism of the distal and proximal phalanges of the thumb": [ + "HP:0009656" + ], + "triangular shape thumb phalanx": [ + "HP:0009657" + ], + "triangular shaped thumb phalanx": [ + "HP:0009657" + ], + "triangular shape phalanx of the thumb": [ + "HP:0009657" + ], + "triangular shaped phalanges of the thumb": [ + "HP:0009657" + ], + "triangular shape thumb bone": [ + "HP:0009657" + ], + "triangular shaped thumb bone": [ + "HP:0009657" + ], + "triangular thumb phalanx": [ + "HP:0009657" + ], + "triangular thumb phalanges": [ + "HP:0009657" + ], + "aplasia / hypoplasia of the phalanx of the thumb": [ + "HP:0009658" + ], + "aplasia / hypoplasia of the phalanges of the thumb": [ + "HP:0009658" + ], + "absent / small thumb bone": [ + "HP:0009658" + ], + "absent / small thumb bones": [ + "HP:0009658" + ], + "absent / underdevelop thumb bone": [ + "HP:0009658" + ], + "absent / underdeveloped thumb bones": [ + "HP:0009658" + ], + "partial absence of thumb": [ + "HP:0009659" + ], + "aplasia of the phalanx of the thumb": [ + "HP:0009659" + ], + "aplasia of the phalanges of the thumb": [ + "HP:0009659" + ], + "short phalanx of the thumb": [ + "HP:0009660" + ], + "hypoplastic thumb phalanx": [ + "HP:0009660" + ], + "hypoplastic thumb phalanges": [ + "HP:0009660" + ], + "hypoplastic / small phalanx of the thumb": [ + "HP:0009660" + ], + "hypoplastic / small phalanges of the thumb": [ + "HP:0009660" + ], + "short thumb bone": [ + "HP:0009660" + ], + "short thumb phalanx": [ + "HP:0009660" + ], + "short thumb phalanges": [ + "HP:0009660" + ], + "abnormality of the epiphysis of the distal phalanx of the thumb": [ + "HP:0009662" + ], + "abnormality of terminal thumb epiphysis": [ + "HP:0009662" + ], + "abnormality of the end part of the outermost bone of the thumb": [ + "HP:0009662" + ], + "abnormality of the epiphysis of the proximal phalanx of the thumb": [ + "HP:0009663" + ], + "abnormality of end part of thumb innermost long bone": [ + "HP:0009663" + ], + "absent epiphysis of the proximal phalanx of the thumb": [ + "HP:0009664" + ], + "absent end part of thumb innermost long bone": [ + "HP:0009664" + ], + "bracket epiphysis of the proximal phalanx of the thumb": [ + "HP:0009665" + ], + "bracket shape end part of thumb innermost long bone": [ + "HP:0009665" + ], + "bracket shaped end part of thumb innermost long bone": [ + "HP:0009665" + ], + "cone - shaped epiphysis of the proximal phalanx of the thumb": [ + "HP:0009666" + ], + "cone - shaped end part of thumb innermost long bone": [ + "HP:0009666" + ], + "enlarged epiphysis of the proximal phalanx of the thumb": [ + "HP:0009667" + ], + "enlarged end part of thumb innermost long bone": [ + "HP:0009667" + ], + "fragmentation of the epiphysis of the proximal phalanx of the thumb": [ + "HP:0009668" + ], + "fragmentation of end part of thumb innermost long bone": [ + "HP:0009668" + ], + "irregular epiphysis of the proximal phalanx of the thumb": [ + "HP:0009669" + ], + "irregular end part of thumb innermost long bone": [ + "HP:0009669" + ], + "ivory epiphysis of the proximal phalanx of the thumb": [ + "HP:0009670" + ], + "increase bone density of end part of the innermost bone of the thumb": [ + "HP:0009670" + ], + "increased bone density of end part of the innermost bone of the thumb": [ + "HP:0009670" + ], + "pseudoepiphysis of the proximal phalanx of the thumb": [ + "HP:0009671" + ], + "small epiphysis of the proximal phalanx of the thumb": [ + "HP:0009672" + ], + "small end part of thumb innermost long bone": [ + "HP:0009672" + ], + "stippling of the epiphysis of the proximal phalanx of the thumb": [ + "HP:0009673" + ], + "speckled calcification in end part of thumb innermost long bone": [ + "HP:0009673" + ], + "speckled calcifications in end part of thumb innermost long bone": [ + "HP:0009673" + ], + "triangular epiphysis of the proximal phalanx of the thumb": [ + "HP:0009674" + ], + "triangular end part of thumb innermost long bone": [ + "HP:0009674" + ], + "absent epiphysis of the distal phalanx of the thumb": [ + "HP:0009675" + ], + "absent end part of thumb outermost long bone": [ + "HP:0009675" + ], + "bracket epiphysis of the distal phalanx of the thumb": [ + "HP:0009676" + ], + "bracket shape end part of thumb outermost long bone": [ + "HP:0009676" + ], + "bracket shaped end part of thumb outermost long bone": [ + "HP:0009676" + ], + "cone - shaped epiphysis of the distal phalanx of the thumb": [ + "HP:0009677" + ], + "cone - shaped end part of thumb outermost long bone": [ + "HP:0009677" + ], + "cone - shape terminal thumb phalanx epiphysis": [ + "HP:0009677" + ], + "cone - shaped terminal thumb phalanx epiphysis": [ + "HP:0009677" + ], + "enlarged epiphysis of the distal phalanx of the thumb": [ + "HP:0009678" + ], + "enlarged end part of thumb outermost long bone": [ + "HP:0009678" + ], + "large terminal thumb phalanx epiphysis": [ + "HP:0009678" + ], + "fragmentation of the epiphysis of the distal phalanx of the thumb": [ + "HP:0009679" + ], + "fragmentation of end part thumb outermost long bone": [ + "HP:0009679" + ], + "irregular epiphysis of the distal phalanx of the thumb": [ + "HP:0009680" + ], + "irregular end part of thumb outermost bone": [ + "HP:0009680" + ], + "ivory epiphysis of the distal phalanx of the thumb": [ + "HP:0009681" + ], + "increase bone density of end part of the outermost bone of the thumb": [ + "HP:0009681" + ], + "increased bone density of end part of the outermost bone of the thumb": [ + "HP:0009681" + ], + "pseudoepiphysis of the distal phalanx of the thumb": [ + "HP:0009682" + ], + "pseudoepiphysis of the outermost bone of the thumb": [ + "HP:0009682" + ], + "small epiphysis of the distal phalanx of the thumb": [ + "HP:0009683" + ], + "small end part of thumb outermost bone": [ + "HP:0009683" + ], + "stippling of the epiphysis of the distal phalanx of the thumb": [ + "HP:0009684" + ], + "speckled calcification in the end part of the outermost thumb bone": [ + "HP:0009684" + ], + "speckled calcifications in the end part of the outermost thumb bone": [ + "HP:0009684" + ], + "triangular epiphysis of the distal phalanx of the thumb": [ + "HP:0009685" + ], + "triangular end part of thumb outermost bone": [ + "HP:0009685" + ], + "triangular epiphysis of the outermost bone of the thumb": [ + "HP:0009685" + ], + "absent epiphysis of the thumb": [ + "HP:0009686" + ], + "absent epiphyses of the thumb": [ + "HP:0009686" + ], + "bracket epiphysis of the thumb": [ + "HP:0009687" + ], + "bracket epiphyses of the thumb": [ + "HP:0009687" + ], + "bracket shape end part of the thumb bone": [ + "HP:0009687" + ], + "bracket shaped end part of the thumb bone": [ + "HP:0009687" + ], + "cone - shaped epiphysis of the thumb": [ + "HP:0009688" + ], + "cone - shaped end part of thumb long bone": [ + "HP:0009688" + ], + "cone - shaped epiphyses of the thumb": [ + "HP:0009688" + ], + "cone - shaped thumb epiphysis": [ + "HP:0009688" + ], + "cone - shaped thumb epiphyses": [ + "HP:0009688" + ], + "enlarge thumb epiphysis": [ + "HP:0009689" + ], + "enlarged thumb epiphysis": [ + "HP:0009689" + ], + "enlarged end part of thumb long bone": [ + "HP:0009689" + ], + "enlarged epiphysis of the thumb": [ + "HP:0009689" + ], + "enlarged epiphyses of the thumb": [ + "HP:0009689" + ], + "fragmentation of thumb epiphysis": [ + "HP:0009690" + ], + "fragmentation of end part of long bone of thumb": [ + "HP:0009690" + ], + "fragmentation of the epiphysis of the thumb": [ + "HP:0009690" + ], + "fragmentation of the epiphyses of the thumb": [ + "HP:0009690" + ], + "irregular thumb epiphysis": [ + "HP:0009691" + ], + "irregular end part of thumb long bone": [ + "HP:0009691" + ], + "irregular epiphysis of the thumb": [ + "HP:0009691" + ], + "irregular epiphyses of the thumb": [ + "HP:0009691" + ], + "ivory epiphysis of the thumb": [ + "HP:0009692" + ], + "increase bone density of end part of the thumb": [ + "HP:0009692" + ], + "increased bone density of end part of the thumb": [ + "HP:0009692" + ], + "ivory epiphyses of the thumb": [ + "HP:0009692" + ], + "pseudoepiphysis of the thumb": [ + "HP:0009693" + ], + "pseudoepiphyses of the thumb": [ + "HP:0009693" + ], + "small thumb epiphysis": [ + "HP:0009694" + ], + "small end part of thumb long bone": [ + "HP:0009694" + ], + "small epiphysis of the thumb": [ + "HP:0009694" + ], + "small epiphyses of the thumb": [ + "HP:0009694" + ], + "stippling of thumb epiphysis": [ + "HP:0009695" + ], + "speckled calcification in end part of thumb bone": [ + "HP:0009695" + ], + "speckled calcifications in end part of thumb bone": [ + "HP:0009695" + ], + "stippling of the epiphysis of the thumb": [ + "HP:0009695" + ], + "stippling of the epiphyses of the thumb": [ + "HP:0009695" + ], + "triangular epiphysis of the thumb": [ + "HP:0009696" + ], + "triangular epiphyses of the thumb": [ + "HP:0009696" + ], + "triangular end part of the thumb bone": [ + "HP:0009696" + ], + "contracture of the distal interphalangeal joint of the finger": [ + "HP:0009697" + ], + "contracture of the distal interphalangeal joint of the fingers": [ + "HP:0009697" + ], + "osteolytic defect of the hand bone": [ + "HP:0009699" + ], + "osteolytic defects of the hand bones": [ + "HP:0009699" + ], + "lytic defect of hand bone": [ + "HP:0009699" + ], + "lytic defects of hand bones": [ + "HP:0009699" + ], + "finger symphalangism": [ + "HP:0009700" + ], + "fuse finger bone": [ + "HP:0009700" + ], + "fused finger bones": [ + "HP:0009700" + ], + "symphalangism of the hand": [ + "HP:0009700" + ], + "synostosis involve bone of the finger": [ + "HP:0009700" + ], + "synostosis involving bones of the fingers": [ + "HP:0009700" + ], + "metacarpal synostosis": [ + "HP:0009701" + ], + "fuse long bone of hand": [ + "HP:0009701" + ], + "fused long bones of hand": [ + "HP:0009701" + ], + "synostosis involve metacarpal bone": [ + "HP:0009701" + ], + "synostosis involving metacarpal bones": [ + "HP:0009701" + ], + "synostosis involve the metacarpal bone": [ + "HP:0009701" + ], + "synostosis involving the metacarpal bones": [ + "HP:0009701" + ], + "carpal synostosis": [ + "HP:0009702" + ], + "carpal bone fusion": [ + "HP:0009702" + ], + "carpal fusion": [ + "HP:0009702" + ], + "fuse carpal bone": [ + "HP:0009702" + ], + "fused carpal bones": [ + "HP:0009702" + ], + "fuse wrist bone": [ + "HP:0009702" + ], + "fused wrist bones": [ + "HP:0009702" + ], + "fusion of carpal bone": [ + "HP:0009702" + ], + "fusion of carpal bones": [ + "HP:0009702" + ], + "synostosis involve the carpal bone": [ + "HP:0009702" + ], + "synostosis involving the carpal bones": [ + "HP:0009702" + ], + "synostosis involve the 1st metacarpal": [ + "HP:0009703" + ], + "synostosis involving the 1st metacarpal": [ + "HP:0009703" + ], + "first metacarpophalangeal joint synostosis": [ + "HP:0009703" + ], + "fusion involve 1st long bone of hand": [ + "HP:0009703" + ], + "fusion involving 1st long bone of hand": [ + "HP:0009703" + ], + "symphalangism affect the 1st metacarpal": [ + "HP:0009703" + ], + "symphalangism affecting the 1st metacarpal": [ + "HP:0009703" + ], + "chronic csf lymphocytosis": [ + "HP:0009704" + ], + "chronic cerebrospinal fluid lymphocytosis": [ + "HP:0009704" + ], + "synostosis involve the 2nd metacarpal": [ + "HP:0009705" + ], + "synostosis involving the 2nd metacarpal": [ + "HP:0009705" + ], + "fusion involve the 2nd long bone of hand": [ + "HP:0009705" + ], + "fusion involving the 2nd long bone of hand": [ + "HP:0009705" + ], + "synostosis involve the 3rd metacarpal": [ + "HP:0009706" + ], + "synostosis involving the 3rd metacarpal": [ + "HP:0009706" + ], + "fusion involve the 3rd long bone of hand": [ + "HP:0009706" + ], + "fusion involving the 3rd long bone of hand": [ + "HP:0009706" + ], + "synostosis involve the 4th metacarpal": [ + "HP:0009707" + ], + "synostosis involving the 4th metacarpal": [ + "HP:0009707" + ], + "fusion involve the 4th long bone of hand": [ + "HP:0009707" + ], + "fusion involving the 4th long bone of hand": [ + "HP:0009707" + ], + "synostosis involve the 5th metacarpal": [ + "HP:0009708" + ], + "synostosis involving the 5th metacarpal": [ + "HP:0009708" + ], + "fusion involve the 5th long bone of hand": [ + "HP:0009708" + ], + "fusion involving the 5th long bone of hand": [ + "HP:0009708" + ], + "increase csf interferon alpha": [ + "HP:0009709" + ], + "increased csf interferon alpha": [ + "HP:0009709" + ], + "chilblain": [ + "HP:0009710" + ], + "chilblains": [ + "HP:0009710" + ], + "chilblain lesion": [ + "HP:0009710" + ], + "chilblain lesions": [ + "HP:0009710" + ], + "retinal capillary hemangioma": [ + "HP:0009711" + ], + "retinal hemangioblastoma": [ + "HP:0009711" + ], + "spinal hemangioblastoma": [ + "HP:0009713" + ], + "abnormality of the epididymis": [ + "HP:0009714" + ], + "papillary cystadenoma of the epididymis": [ + "HP:0009715" + ], + "subependymal nodule": [ + "HP:0009716" + ], + "subependymal nodules": [ + "HP:0009716" + ], + "cortical tuber": [ + "HP:0009717" + ], + "cortical tubers": [ + "HP:0009717" + ], + "subependymal giant - cell astrocytoma": [ + "HP:0009718" + ], + "hypomelanotic macule": [ + "HP:0009719" + ], + "hypomelanotic macules": [ + "HP:0009719" + ], + "adenoma sebaceum": [ + "HP:0009720" + ], + "facial angiofibromas": [ + "HP:0009720" + ], + "sebaceous adenoma": [ + "HP:0009720" + ], + "sebaceous adenomas": [ + "HP:0009720" + ], + "shagreen patch": [ + "HP:0009721" + ], + "dental enamel pit": [ + "HP:0009722" + ], + "dental enamel pits": [ + "HP:0009722" + ], + "dental enamel pitting": [ + "HP:0009722" + ], + "pitting of tooth enamel": [ + "HP:0009722" + ], + "tooth enamel pit": [ + "HP:0009722" + ], + "tooth enamel pits": [ + "HP:0009722" + ], + "abnormality of the subungual region": [ + "HP:0009723" + ], + "subungual fibroma": [ + "HP:0009724" + ], + "subungual fibromas": [ + "HP:0009724" + ], + "bladder neoplasm": [ + "HP:0009725" + ], + "bladder cancer": [ + "HP:0009725" + ], + "bladder tumor": [ + "HP:0009725" + ], + "bladder tumour": [ + "HP:0009725" + ], + "renal neoplasm": [ + "HP:0009726" + ], + "kidney cancer": [ + "HP:0009726" + ], + "neoplasia of the kidney": [ + "HP:0009726" + ], + "neoplasia of the kidneys": [ + "HP:0009726" + ], + "renal neoplasia": [ + "HP:0009726" + ], + "renal tumor": [ + "HP:0009726" + ], + "renal tumors": [ + "HP:0009726" + ], + "renal tumour": [ + "HP:0009726" + ], + "renal tumours": [ + "HP:0009726" + ], + "achromatic retinal patch": [ + "HP:0009727" + ], + "achromatic retinal patches": [ + "HP:0009727" + ], + "punch out area of chorioretinal hypopigmentation": [ + "HP:0009727" + ], + "punched out areas of chorioretinal hypopigmentation": [ + "HP:0009727" + ], + "neoplasm of striated muscle": [ + "HP:0009728" + ], + "tumor of striated muscle": [ + "HP:0009728" + ], + "tumors of striated muscle": [ + "HP:0009728" + ], + "tumour of striated muscle": [ + "HP:0009728" + ], + "tumours of striated muscle": [ + "HP:0009728" + ], + "cardiac rhabdomyoma": [ + "HP:0009729" + ], + "rhabdomyoma": [ + "HP:0009730" + ], + "cerebral hamartoma": [ + "HP:0009731" + ], + "cerebral hamartomata": [ + "HP:0009731" + ], + "plexiform neurofibroma": [ + "HP:0009732" + ], + "glioma": [ + "HP:0009733" + ], + "optic nerve glioma": [ + "HP:0009734" + ], + "optic glioma": [ + "HP:0009734" + ], + "spinal neurofibroma": [ + "HP:0009735" + ], + "spinal neurofibromas": [ + "HP:0009735" + ], + "tibial pseudarthrosis": [ + "HP:0009736" + ], + "tibial pseudoarthrosis": [ + "HP:0009736" + ], + "lisch nodule": [ + "HP:0009737" + ], + "lisch nodules": [ + "HP:0009737" + ], + "iris hamartoma": [ + "HP:0009737" + ], + "iris hamartomas": [ + "HP:0009737" + ], + "abnormality of the antihelix": [ + "HP:0009738" + ], + "abnormal antehelix": [ + "HP:0009738" + ], + "abnormal anthelix": [ + "HP:0009738" + ], + "abnormal antihelix": [ + "HP:0009738" + ], + "hypoplasia of the antihelix": [ + "HP:0009739" + ], + "hypoplastic antihelix": [ + "HP:0009739" + ], + "aplasia of the parotid gland": [ + "HP:0009740" + ], + "abnormally small parotid gland": [ + "HP:0009740" + ], + "absence of the parotid gland": [ + "HP:0009740" + ], + "hypoplasia of parotid gland": [ + "HP:0009740" + ], + "underdevelopment of parotid gland": [ + "HP:0009740" + ], + "nephrosclerosis": [ + "HP:0009741" + ], + "scarring of kidney artery": [ + "HP:0009741" + ], + "scarring of kidney arteries": [ + "HP:0009741" + ], + "thickening of kidney artiries": [ + "HP:0009741" + ], + "stiff shoulder": [ + "HP:0009742" + ], + "stiff shoulders": [ + "HP:0009742" + ], + "distichiasis": [ + "HP:0009743" + ], + "distichiasis of eyelid eyelash": [ + "HP:0009743" + ], + "distichiasis of eyelid eyelashes": [ + "HP:0009743" + ], + "abnormal spinal dura mater morphology": [ + "HP:0009744" + ], + "abnormality of the spinal dura mater": [ + "HP:0009744" + ], + "spinal arachnoid cyst": [ + "HP:0009745" + ], + "epidural arachnoid cyst of the spinal canal": [ + "HP:0009745" + ], + "epidural arachnoid cysts of the spinal canal": [ + "HP:0009745" + ], + "thick nasal septum": [ + "HP:0009746" + ], + "broad nasal septum": [ + "HP:0009746" + ], + "broad septum of nose": [ + "HP:0009746" + ], + "thick septum of nose": [ + "HP:0009746" + ], + "wide nasal septum": [ + "HP:0009746" + ], + "wide septum of nose": [ + "HP:0009746" + ], + "lumbosacral hirsutism": [ + "HP:0009747" + ], + "large earlobe": [ + "HP:0009748" + ], + "fleshy earlobe": [ + "HP:0009748" + ], + "fleshy earlobes": [ + "HP:0009748" + ], + "prominent ear lobe": [ + "HP:0009748" + ], + "prominent ear lobes": [ + "HP:0009748" + ], + "prominent ear lobule": [ + "HP:0009748" + ], + "prominent ear lobules": [ + "HP:0009748" + ], + "aplasia of the pectoralis major muscle": [ + "HP:0009751" + ], + "absent pectoralis major muscle": [ + "HP:0009751" + ], + "cleft in skull base": [ + "HP:0009752" + ], + "cleft in cranial base": [ + "HP:0009752" + ], + "fibrous syngnathia": [ + "HP:0009754" + ], + "alveolar synechiae": [ + "HP:0009754" + ], + "fusion of the alveolar ridge": [ + "HP:0009754" + ], + "fusion of the alveolar ridges": [ + "HP:0009754" + ], + "ankyloblepharon": [ + "HP:0009755" + ], + "adhesion of eyelid": [ + "HP:0009755" + ], + "adhesion of eyelids": [ + "HP:0009755" + ], + "ankyloblepharon filiforme adnatum": [ + "HP:0009755" + ], + "eyelid synechiae": [ + "HP:0009755" + ], + "eyelid stick together": [ + "HP:0009755" + ], + "eyelids stuck together": [ + "HP:0009755" + ], + "popliteal pterygium": [ + "HP:0009756" + ], + "intercrural pterygium": [ + "HP:0009757" + ], + "pyramidal skinfold extend from the base to the top of the nail": [ + "HP:0009758" + ], + "pyramidal skinfold extending from the base to the top of the nails": [ + "HP:0009758" + ], + "neck pterygium": [ + "HP:0009759" + ], + "neck pterygia": [ + "HP:0009759" + ], + "antecubital pterygium": [ + "HP:0009760" + ], + "pterygium cubitale": [ + "HP:0009760" + ], + "web elbow": [ + "HP:0009760" + ], + "webbed elbow": [ + "HP:0009760" + ], + "anterior clefting of vertebral body": [ + "HP:0009761" + ], + "anterior clefting of vertebral bodies": [ + "HP:0009761" + ], + "facial wrinkling": [ + "HP:0009762" + ], + "limb pain": [ + "HP:0009763" + ], + "pain in extremity": [ + "HP:0009763" + ], + "pain in extremities": [ + "HP:0009763" + ], + "low hang columella": [ + "HP:0009765" + ], + "low hanging columella": [ + "HP:0009765" + ], + "columella extend below the ala nasi": [ + "HP:0009765" + ], + "columella extends below the ala nasi": [ + "HP:0009765" + ], + "columella , low": [ + "HP:0009765" + ], + "columella , low hanging": [ + "HP:0009765" + ], + "extension of the columella below the ala nasi": [ + "HP:0009765" + ], + "low - hanging columella": [ + "HP:0009765" + ], + "prominent columella": [ + "HP:0009765" + ], + "round columella": [ + "HP:0009765" + ], + "rounded columella": [ + "HP:0009765" + ], + "aplasia / hypoplasia of the phalanx of the hand": [ + "HP:0009767" + ], + "aplasia / hypoplasia of the phalanges of the hand": [ + "HP:0009767" + ], + "aplastic / hypoplastic phalanx": [ + "HP:0009767" + ], + "aplastic / hypoplastic phalanges": [ + "HP:0009767" + ], + "aplastic / hypoplastic phalanx of the hand": [ + "HP:0009767" + ], + "aplastic / hypoplastic phalanges of the hand": [ + "HP:0009767" + ], + "hypoplastic / absent phalanx": [ + "HP:0009767" + ], + "hypoplastic / absent phalanges": [ + "HP:0009767" + ], + "broad phalanx of the hand": [ + "HP:0009768" + ], + "broad phalanges of the hand": [ + "HP:0009768" + ], + "wide hand bone": [ + "HP:0009768" + ], + "wide hand bones": [ + "HP:0009768" + ], + "widening of phalanx of the hand": [ + "HP:0009768" + ], + "widening of phalanges of the hand": [ + "HP:0009768" + ], + "bullet - shaped phalanx of the hand": [ + "HP:0009769" + ], + "bullet - shaped phalanges of the hand": [ + "HP:0009769" + ], + "bullet - shaped hand bone": [ + "HP:0009769" + ], + "bullet - shaped hand bones": [ + "HP:0009769" + ], + "bullet - shaped phalanges of the hands": [ + "HP:0009769" + ], + "conical bullet - shaped distal end of phalanx": [ + "HP:0009769" + ], + "conical bullet - shaped distal ends of phalanges": [ + "HP:0009769" + ], + "curve phalanx of the hand": [ + "HP:0009770" + ], + "curved phalanges of the hand": [ + "HP:0009770" + ], + "curve hand bone": [ + "HP:0009770" + ], + "curved hand bones": [ + "HP:0009770" + ], + "osteolytic defect of the phalanx of the hand": [ + "HP:0009771" + ], + "osteolytic defects of the phalanges of the hand": [ + "HP:0009771" + ], + "acro - osteolysis": [ + "HP:0009771" + ], + "acroosteolysis": [ + "HP:0009771" + ], + "breakdown of small bone of finger": [ + "HP:0009771" + ], + "breakdown of small bones of fingers": [ + "HP:0009771" + ], + "patchy sclerosis of finger phalanx": [ + "HP:0009772" + ], + "patchy sclerosis of the phalanx of the hand": [ + "HP:0009772" + ], + "patchy sclerosis of the phalanges of the hand": [ + "HP:0009772" + ], + "phalangeal sclerosis": [ + "HP:0009772" + ], + "uneven increase in bone density in finger bone": [ + "HP:0009772" + ], + "symphalangism affect the phalanx of the hand": [ + "HP:0009773" + ], + "symphalangism affecting the phalanges of the hand": [ + "HP:0009773" + ], + "fuse finger bone of the hand": [ + "HP:0009773" + ], + "fused finger bones of the hand": [ + "HP:0009773" + ], + "synostosis involve phalanx of the hand": [ + "HP:0009773" + ], + "synostosis involving phalanges of the hand": [ + "HP:0009773" + ], + "triangular shape phalanx of the hand": [ + "HP:0009774" + ], + "triangular shaped phalanges of the hand": [ + "HP:0009774" + ], + "delta phalanx / delta - like phalanx": [ + "HP:0009774" + ], + "triangular shape hand bone": [ + "HP:0009774" + ], + "triangular shaped hand bones": [ + "HP:0009774" + ], + "amniotic constriction ring": [ + "HP:0009775" + ], + "amniotic band": [ + "HP:0009775" + ], + "amniotic bands": [ + "HP:0009775" + ], + "amniotic constriction band": [ + "HP:0009775" + ], + "pseudoainhum": [ + "HP:0009775" + ], + "adactyly": [ + "HP:0009776" + ], + "absent finger or toe": [ + "HP:0009776" + ], + "absent fingers or toes": [ + "HP:0009776" + ], + "aphalangy": [ + "HP:0009776" + ], + "absent thumb": [ + "HP:0009777" + ], + "absent thumbs": [ + "HP:0009777" + ], + "aplasia of the thumb": [ + "HP:0009777" + ], + "thumb aplasia": [ + "HP:0009777" + ], + "short thumb": [ + "HP:0009778" + ], + "hypoplastic thumb": [ + "HP:0009778" + ], + "hypoplastic thumbs": [ + "HP:0009778" + ], + "hypoplastic / small thumb": [ + "HP:0009778" + ], + "short thumbs": [ + "HP:0009778" + ], + "small thumb": [ + "HP:0009778" + ], + "small thumbs": [ + "HP:0009778" + ], + "thumb brachydactyly": [ + "HP:0009778" + ], + "thumb hypoplasia": [ + "HP:0009778" + ], + "3 - 4 toe syndactyly": [ + "HP:0009779" + ], + "syndactyly of 3rd - 4th toe": [ + "HP:0009779" + ], + "syndactyly of 3rd - 4th toes": [ + "HP:0009779" + ], + "web 3rd - 4th toe": [ + "HP:0009779" + ], + "webbed 3rd - 4th toes": [ + "HP:0009779" + ], + "iliac horn": [ + "HP:0009780" + ], + "iliac horns": [ + "HP:0009780" + ], + "lester 's sign": [ + "HP:0009781" + ], + "aplasia / hypoplasia of the biceps": [ + "HP:0009782" + ], + "absent / small biceps": [ + "HP:0009782" + ], + "absent / underdevelop biceps": [ + "HP:0009782" + ], + "absent / underdeveloped biceps": [ + "HP:0009782" + ], + "biceps aplasia": [ + "HP:0009783" + ], + "absent biceps": [ + "HP:0009783" + ], + "aplasia / hypoplasia of the triceps": [ + "HP:0009784" + ], + "absent / small triceps": [ + "HP:0009784" + ], + "absent / underdevelop triceps": [ + "HP:0009784" + ], + "absent / underdeveloped triceps": [ + "HP:0009784" + ], + "triceps aplasia": [ + "HP:0009785" + ], + "absent triceps": [ + "HP:0009785" + ], + "aplasia / hypoplasia of the musculature of the thigh": [ + "HP:0009786" + ], + "absent / small thigh muscle": [ + "HP:0009786" + ], + "absent / small thigh muscles": [ + "HP:0009786" + ], + "absent / underdevelop thigh muscle": [ + "HP:0009786" + ], + "absent / underdeveloped thigh muscles": [ + "HP:0009786" + ], + "aplasia / hypoplasia of the quadriceps": [ + "HP:0009787" + ], + "absent / small quadriceps": [ + "HP:0009787" + ], + "absent / underdevelop quadriceps": [ + "HP:0009787" + ], + "absent / underdeveloped quadriceps": [ + "HP:0009787" + ], + "quadriceps aplasia": [ + "HP:0009788" + ], + "absent quad": [ + "HP:0009788" + ], + "absent quads": [ + "HP:0009788" + ], + "perianal abscess": [ + "HP:0009789" + ], + "hemisacrum": [ + "HP:0009790" + ], + "bifid sacrum": [ + "HP:0009791" + ], + "teratoma": [ + "HP:0009792" + ], + "presacral teratoma": [ + "HP:0009793" + ], + "altman type iv sacrococcygeal teratoma": [ + "HP:0009793" + ], + "retrorectal teratoma": [ + "HP:0009793" + ], + "branchial anomaly": [ + "HP:0009794" + ], + "abnormality of branchial apparatus": [ + "HP:0009794" + ], + "abnormality of branchial arch": [ + "HP:0009794" + ], + "branchial abnormality": [ + "HP:0009794" + ], + "branchial anomalies": [ + "HP:0009794" + ], + "branchial fistula": [ + "HP:0009795" + ], + "branchial cleft fistula": [ + "HP:0009795" + ], + "branchial cyst": [ + "HP:0009796" + ], + "branchial cleft cyst": [ + "HP:0009796" + ], + "branchial cysts": [ + "HP:0009796" + ], + "cholesteatoma": [ + "HP:0009797" + ], + "euthyroid goiter": [ + "HP:0009798" + ], + "euthyroid goitre": [ + "HP:0009798" + ], + "supernumerary spleen": [ + "HP:0009799" + ], + "supernumerary spleens": [ + "HP:0009799" + ], + "extra spleen": [ + "HP:0009799" + ], + "maternal diabetes": [ + "HP:0009800" + ], + "gestational diabetes": [ + "HP:0009800" + ], + "maternal hyperglycemia": [ + "HP:0009800" + ], + "aplasia of the phalanx of the hand": [ + "HP:0009802" + ], + "aplasia of the phalanges of the hand": [ + "HP:0009802" + ], + "absent finger bone of the hand": [ + "HP:0009802" + ], + "short phalanx of finger": [ + "HP:0009803" + ], + "hypoplastic phalanx": [ + "HP:0009803" + ], + "hypoplastic phalanges": [ + "HP:0009803" + ], + "hypoplastic phalanx of hand": [ + "HP:0009803" + ], + "hypoplastic phalanges of hands": [ + "HP:0009803" + ], + "hypoplastic / small phalanx of the hand": [ + "HP:0009803" + ], + "hypoplastic / small phalanges of the hand": [ + "HP:0009803" + ], + "phalangeal hypoplasia": [ + "HP:0009803" + ], + "rudimentary phalanx": [ + "HP:0009803" + ], + "rudimentary phalanges": [ + "HP:0009803" + ], + "short finger bone": [ + "HP:0009803" + ], + "short finger bones": [ + "HP:0009803" + ], + "short phalanx": [ + "HP:0009803" + ], + "short phalanges": [ + "HP:0009803" + ], + "shorten phalanx": [ + "HP:0009803" + ], + "shortened phalanges": [ + "HP:0009803" + ], + "tooth agenesis": [ + "HP:0009804" + ], + "decreased number of teeth": [ + "HP:0009804" + ], + "decrease tooth count": [ + "HP:0009804" + ], + "decreased tooth count": [ + "HP:0009804" + ], + "dental agenesis": [ + "HP:0009804" + ], + "failure of development of some teeth": [ + "HP:0009804" + ], + "few teeth than normal": [ + "HP:0009804" + ], + "fewer teeth than normal": [ + "HP:0009804" + ], + "miss some teeth": [ + "HP:0009804" + ], + "missing some teeth": [ + "HP:0009804" + ], + "reduced number of teeth": [ + "HP:0009804" + ], + "teeth , agenesis": [ + "HP:0009804" + ], + "low - output congestive heart failure": [ + "HP:0009805" + ], + "nephrogenic diabetes insipidus": [ + "HP:0009806" + ], + "anomaly of the upper limb diaphysis": [ + "HP:0009808" + ], + "anomaly of the upper limb diaphyses": [ + "HP:0009808" + ], + "abnormality involve the diaphysis of the upper limb": [ + "HP:0009808" + ], + "abnormality involving the diaphyses of the upper limbs": [ + "HP:0009808" + ], + "abnormality of shaft of long bone of the upper limb": [ + "HP:0009808" + ], + "abnormality of shaft of long bone of the upper limbs": [ + "HP:0009808" + ], + "diaphyseal abnormality of the upper limb": [ + "HP:0009808" + ], + "diaphyseal abnormality of the upper limbs": [ + "HP:0009808" + ], + "abnormality of upper limb metaphysis": [ + "HP:0009809" + ], + "abnormality of the wide portion of upper limb bone": [ + "HP:0009809" + ], + "metaphyseal abnormality of the upper limb": [ + "HP:0009809" + ], + "metaphyseal abnormality of the upper limbs": [ + "HP:0009809" + ], + "abnormality of upper limb joint": [ + "HP:0009810" + ], + "abnormality of the joint of the upper limb": [ + "HP:0009810" + ], + "abnormality of the joints of the upper limbs": [ + "HP:0009810" + ], + "abnormality of the elbow": [ + "HP:0009811" + ], + "abnormality of the elbows": [ + "HP:0009811" + ], + "amelia involve the upper limb": [ + "HP:0009812" + ], + "amelia involving the upper limbs": [ + "HP:0009812" + ], + "upper limb phocomelia": [ + "HP:0009813" + ], + "upper limb peromelia": [ + "HP:0009814" + ], + "aplasia / hypoplasia of the extremity": [ + "HP:0009815" + ], + "aplasia / hypoplasia of the extremities": [ + "HP:0009815" + ], + "absent / small extremity": [ + "HP:0009815" + ], + "absent / small extremities": [ + "HP:0009815" + ], + "absent / underdevelop extremity": [ + "HP:0009815" + ], + "absent / underdeveloped extremities": [ + "HP:0009815" + ], + "short or absent limb": [ + "HP:0009815" + ], + "short or absent limbs": [ + "HP:0009815" + ], + "shorten limb": [ + "HP:0009815" + ], + "shortened limbs": [ + "HP:0009815" + ], + "low limb undergrowth": [ + "HP:0009816" + ], + "lower limb undergrowth": [ + "HP:0009816" + ], + "hypoplasia involve bone of the low limb": [ + "HP:0009816" + ], + "hypoplasia involving bones of the lower limbs": [ + "HP:0009816" + ], + "hypoplasia of the low limb": [ + "HP:0009816" + ], + "hypoplasia of the lower limbs": [ + "HP:0009816" + ], + "underdeveloped low limb bone": [ + "HP:0009816" + ], + "underdeveloped lower limb bones": [ + "HP:0009816" + ], + "aplasia involve bone of the low limb": [ + "HP:0009817" + ], + "aplasia involving bones of the lower limbs": [ + "HP:0009817" + ], + "absent bone of the low limb": [ + "HP:0009817" + ], + "absent bones of the lower limbs": [ + "HP:0009817" + ], + "amelia involve the low limb": [ + "HP:0009818" + ], + "amelia involving the lower limbs": [ + "HP:0009818" + ], + "low limb phocomelia": [ + "HP:0009819" + ], + "lower limb phocomelia": [ + "HP:0009819" + ], + "low limb peromelia": [ + "HP:0009820" + ], + "lower limb peromelia": [ + "HP:0009820" + ], + "forearm undergrowth": [ + "HP:0009821" + ], + "hypoplasia involve forearm bone": [ + "HP:0009821" + ], + "hypoplasia involving forearm bones": [ + "HP:0009821" + ], + "short forearm bone": [ + "HP:0009821" + ], + "short forearm bones": [ + "HP:0009821" + ], + "short forearms": [ + "HP:0009821" + ], + "shorten forearm": [ + "HP:0009821" + ], + "shortened forearm": [ + "HP:0009821" + ], + "aplasia involve forearm bone": [ + "HP:0009822" + ], + "aplasia involving forearm bones": [ + "HP:0009822" + ], + "absent forearm bones": [ + "HP:0009822" + ], + "aplasia involve bone of the upper limb": [ + "HP:0009823" + ], + "aplasia involving bones of the upper limbs": [ + "HP:0009823" + ], + "absent bone of the upper limb": [ + "HP:0009823" + ], + "absent bones of the upper limbs": [ + "HP:0009823" + ], + "upper limb undergrowth": [ + "HP:0009824" + ], + "hypoplasia involve bone of the upper limb": [ + "HP:0009824" + ], + "hypoplasia involving bones of the upper limbs": [ + "HP:0009824" + ], + "short arm": [ + "HP:0009824" + ], + "short arms": [ + "HP:0009824" + ], + "shortening of the arm": [ + "HP:0009824" + ], + "shortening of the arms": [ + "HP:0009824" + ], + "aplasia involve bone of the extremity": [ + "HP:0009825" + ], + "aplasia involving bones of the extremities": [ + "HP:0009825" + ], + "absent bone of the extremity": [ + "HP:0009825" + ], + "absent bones of the extremities": [ + "HP:0009825" + ], + "limb undergrowth": [ + "HP:0009826" + ], + "hypoplasia involve bone of the extremity": [ + "HP:0009826" + ], + "hypoplasia involving bones of the extremities": [ + "HP:0009826" + ], + "limb shorten": [ + "HP:0009826" + ], + "limb shortening": [ + "HP:0009826" + ], + "short limb": [ + "HP:0009826" + ], + "short limbs": [ + "HP:0009826" + ], + "amelia": [ + "HP:0009827" + ], + "peromelia": [ + "HP:0009828" + ], + "phocomelia": [ + "HP:0009829" + ], + "peripheral neuropathy": [ + "HP:0009830" + ], + "neuropathy": [ + "HP:0009830" + ], + "peripheral nerve damage": [ + "HP:0009830" + ], + "peripheral neuritis": [ + "HP:0009830" + ], + "mononeuropathy": [ + "HP:0009831" + ], + "single damage nerve": [ + "HP:0009831" + ], + "single damaged nerve": [ + "HP:0009831" + ], + "abnormal distal phalanx morphology of finger": [ + "HP:0009832" + ], + "abnormal terminal phalanx of the hand": [ + "HP:0009832" + ], + "abnormal terminal phalanges of the hand": [ + "HP:0009832" + ], + "abnormality of the distal phalanx of the hand": [ + "HP:0009832" + ], + "abnormality of the distal phalanges of the hand": [ + "HP:0009832" + ], + "abnormality of the distal phalanx of finger": [ + "HP:0009832" + ], + "abnormality of the outermost finger bone": [ + "HP:0009832" + ], + "abnormal middle phalanx morphology of the hand": [ + "HP:0009833" + ], + "abnormality of the middle finger bone of the hand": [ + "HP:0009833" + ], + "abnormality of the middle finger bones of the hand": [ + "HP:0009833" + ], + "abnormality of the middle phalanx of the hand": [ + "HP:0009833" + ], + "abnormality of the middle phalanges of the hand": [ + "HP:0009833" + ], + "abnormal proximal phalanx morphology of the hand": [ + "HP:0009834" + ], + "abnormality of the innermost finger bone of the hand": [ + "HP:0009834" + ], + "abnormality of the innermost finger bones of the hand": [ + "HP:0009834" + ], + "abnormality of the proximal phalanx of the hand": [ + "HP:0009834" + ], + "abnormality of the proximal phalanges of the hand": [ + "HP:0009834" + ], + "aplasia / hypoplasia of the distal phalanx of the hand": [ + "HP:0009835" + ], + "aplasia / hypoplasia of the distal phalanges of the hand": [ + "HP:0009835" + ], + "absent / hypoplastic distal phalanx": [ + "HP:0009835" + ], + "absent / hypoplastic distal phalanges": [ + "HP:0009835" + ], + "absent / small outermost finger bone of the hand": [ + "HP:0009835" + ], + "absent / underdevelop outermost finger bone of the hand": [ + "HP:0009835" + ], + "absent / underdeveloped outermost finger bone of the hand": [ + "HP:0009835" + ], + "aplasia / hypoplasia of the distal phalanx": [ + "HP:0009835" + ], + "aplasia / hypoplasia of the distal phalanges": [ + "HP:0009835" + ], + "aplastic / hypoplastic distal phalanx": [ + "HP:0009835" + ], + "aplastic / hypoplastic distal phalanges": [ + "HP:0009835" + ], + "hypoplastic to absent terminal phalanx": [ + "HP:0009835" + ], + "hypoplastic to absent terminal phalanges": [ + "HP:0009835" + ], + "hypoplastic / aplastic distal phalanx": [ + "HP:0009835" + ], + "hypoplastic / aplastic distal phalanges": [ + "HP:0009835" + ], + "small or absent distal phalanx": [ + "HP:0009835" + ], + "small or absent distal phalanges": [ + "HP:0009835" + ], + "broad distal phalanx of finger": [ + "HP:0009836" + ], + "broad distal phalanx": [ + "HP:0009836" + ], + "broad distal phalanges": [ + "HP:0009836" + ], + "broad distal phalanx of the hand": [ + "HP:0009836" + ], + "broad distal phalanges of the hand": [ + "HP:0009836" + ], + "broad outermost finger bone": [ + "HP:0009836" + ], + "broad terminal phalanx": [ + "HP:0009836" + ], + "broad terminal phalanges": [ + "HP:0009836" + ], + "broad , square end of distal phalanx": [ + "HP:0009836" + ], + "broad , square ends of distal phalanges": [ + "HP:0009836" + ], + "spatulate terminal phalanx": [ + "HP:0009836" + ], + "spatulate terminal phalanges": [ + "HP:0009836" + ], + "bullet - shaped distal phalanx of the hand": [ + "HP:0009837" + ], + "bullet - shaped distal phalanges of the hand": [ + "HP:0009837" + ], + "bullet - shape outermost finger bone of the hand": [ + "HP:0009837" + ], + "bullet - shaped outermost finger bone of the hand": [ + "HP:0009837" + ], + "curve distal phalanx of the hand": [ + "HP:0009838" + ], + "curved distal phalanges of the hand": [ + "HP:0009838" + ], + "curve outermost finger bone of the hand": [ + "HP:0009838" + ], + "curved outermost finger bone of the hand": [ + "HP:0009838" + ], + "osteolytic defect of the distal phalanx of the hand": [ + "HP:0009839" + ], + "osteolytic defects of the distal phalanges of the hand": [ + "HP:0009839" + ], + "acro - osteolysis of distal phalanx": [ + "HP:0009839" + ], + "acro - osteolysis of distal phalanges": [ + "HP:0009839" + ], + "acroosteolysis of distal phalanx": [ + "HP:0009839" + ], + "acroosteolysis of distal phalanges": [ + "HP:0009839" + ], + "osteolytic defect of the outermost finger bone of the hand": [ + "HP:0009839" + ], + "osteolytic defects of the outermost finger bone of the hand": [ + "HP:0009839" + ], + "patchy sclerosis of distal phalanx of finger": [ + "HP:0009840" + ], + "patchy sclerosis of the distal phalanx of the hand": [ + "HP:0009840" + ], + "patchy sclerosis of the distal phalanges of the hand": [ + "HP:0009840" + ], + "uneven increase in bone density in outermost finger bone": [ + "HP:0009840" + ], + "aplasia / hypoplasia of the middle phalanx of the hand": [ + "HP:0009843" + ], + "aplasia / hypoplasia of the middle phalanges of the hand": [ + "HP:0009843" + ], + "absent / hypoplastic middle phalanx": [ + "HP:0009843" + ], + "absent / hypoplastic middle phalanges": [ + "HP:0009843" + ], + "absent / small middle finger bone of the hand": [ + "HP:0009843" + ], + "absent / underdevelop middle finger bone of the hand": [ + "HP:0009843" + ], + "absent / underdeveloped middle finger bone of the hand": [ + "HP:0009843" + ], + "aplasia / hypoplasia of middle phalanx": [ + "HP:0009843" + ], + "aplasia / hypoplasia of middle phalanges": [ + "HP:0009843" + ], + "aplastic / hypoplastic middle phalanx": [ + "HP:0009843" + ], + "aplastic / hypoplastic middle phalanges": [ + "HP:0009843" + ], + "hypoplastic / aplastic middle phalanx": [ + "HP:0009843" + ], + "short to absent middle phalanx": [ + "HP:0009843" + ], + "short to absent middle phalanges": [ + "HP:0009843" + ], + "short / absent middle phalanx": [ + "HP:0009843" + ], + "short / absent middle phalanges": [ + "HP:0009843" + ], + "broad middle phalanx of finger": [ + "HP:0009844" + ], + "broad middle finger bone": [ + "HP:0009844" + ], + "broad middle finger bones": [ + "HP:0009844" + ], + "broad middle phalanges of finger": [ + "HP:0009844" + ], + "broad middle phalanx of the hand": [ + "HP:0009844" + ], + "broad middle phalanges of the hand": [ + "HP:0009844" + ], + "bullet - shape middle phalanx of the hand": [ + "HP:0009845" + ], + "bullet - shaped middle phalanges of the hand": [ + "HP:0009845" + ], + "curve middle phalanx of the hand": [ + "HP:0009846" + ], + "curved middle phalanges of the hand": [ + "HP:0009846" + ], + "curve middle finger bond of the hand": [ + "HP:0009846" + ], + "curved middle finger bonds of the hand": [ + "HP:0009846" + ], + "osteolytic defect of the middle phalanx of the hand": [ + "HP:0009847" + ], + "osteolytic defects of the middle phalanges of the hand": [ + "HP:0009847" + ], + "patchy sclerosis of middle phalanx of finger": [ + "HP:0009848" + ], + "patchy sclerosis of the middle phalanx of the hand": [ + "HP:0009848" + ], + "patchy sclerosis of the middle phalanges of the hand": [ + "HP:0009848" + ], + "uneven increase in bone density in the middle finger bone of the hand": [ + "HP:0009848" + ], + "uneven increase in bone density in the middle finger bones of the hand": [ + "HP:0009848" + ], + "symphalangism of middle phalanx of finger": [ + "HP:0009849" + ], + "fuse middle finger bone": [ + "HP:0009849" + ], + "fused middle finger bone": [ + "HP:0009849" + ], + "triangular shape middle phalanx of the hand": [ + "HP:0009850" + ], + "triangular shaped middle phalanges of the hand": [ + "HP:0009850" + ], + "triangular shape middle finger bone of the hand": [ + "HP:0009850" + ], + "triangular shaped middle finger bones of the hand": [ + "HP:0009850" + ], + "aplasia / hypoplasia of the proximal phalanx of the hand": [ + "HP:0009851" + ], + "aplasia / hypoplasia of the proximal phalanges of the hand": [ + "HP:0009851" + ], + "absent / small innermost finger bone of the hand": [ + "HP:0009851" + ], + "absent / small innermost finger bones of the hand": [ + "HP:0009851" + ], + "absent / underdevelop innermost finger bone of the hand": [ + "HP:0009851" + ], + "absent / underdeveloped innermost finger bones of the hand": [ + "HP:0009851" + ], + "broad proximal phalanx of the hand": [ + "HP:0009852" + ], + "broad proximal phalanges of the hand": [ + "HP:0009852" + ], + "broad innermost finger bone of the hand": [ + "HP:0009852" + ], + "broad innermost finger bones of the hand": [ + "HP:0009852" + ], + "wide innermost finger bone of the hand": [ + "HP:0009852" + ], + "wide innermost finger bones of the hand": [ + "HP:0009852" + ], + "bullet - shape proximal phalanx of the hand": [ + "HP:0009853" + ], + "bullet - shaped proximal phalanges of the hand": [ + "HP:0009853" + ], + "bullet - shape innermost finger bone of the hand": [ + "HP:0009853" + ], + "bullet - shaped innermost finger bones of the hand": [ + "HP:0009853" + ], + "curve proximal phalanx of the hand": [ + "HP:0009854" + ], + "curved proximal phalanges of the hand": [ + "HP:0009854" + ], + "curve innermost finger bone of the hand": [ + "HP:0009854" + ], + "curved innermost finger bones of the hand": [ + "HP:0009854" + ], + "osteolytic defect of the proximal phalanx of the hand": [ + "HP:0009855" + ], + "osteolytic defects of the proximal phalanges of the hand": [ + "HP:0009855" + ], + "proximal phalanx osteolysis": [ + "HP:0009855" + ], + "proximal phalanges osteolysis": [ + "HP:0009855" + ], + "patchy sclerosis of proximal phalanx of finger": [ + "HP:0009856" + ], + "patchy sclerosis of the proximal phalanx of the hand": [ + "HP:0009856" + ], + "patchy sclerosis of the proximal phalanges of the hand": [ + "HP:0009856" + ], + "uneven increase in bone density in innermost finger bone": [ + "HP:0009856" + ], + "symphalangism affect the proximal phalanx of the hand": [ + "HP:0009857" + ], + "symphalangism affecting the proximal phalanges of the hand": [ + "HP:0009857" + ], + "fuse innermost hand bone": [ + "HP:0009857" + ], + "fused innermost hand bones": [ + "HP:0009857" + ], + "triangular shape proximal phalanx of the hand": [ + "HP:0009858" + ], + "triangular shaped proximal phalanges of the hand": [ + "HP:0009858" + ], + "triangular shape innermost finger bone": [ + "HP:0009858" + ], + "triangular shaped innermost finger bone": [ + "HP:0009858" + ], + "triangular shape distal phalanx of the hand": [ + "HP:0009875" + ], + "triangular shaped distal phalanges of the hand": [ + "HP:0009875" + ], + "triangular shape outermost bone of the hand": [ + "HP:0009875" + ], + "triangular shaped outermost bone of the hand": [ + "HP:0009875" + ], + "cerebellar ataxia associate with quadrupedal gait": [ + "HP:0009878" + ], + "cerebellar ataxia associated with quadrupedal gait": [ + "HP:0009878" + ], + "simplify gyral pattern": [ + "HP:0009879" + ], + "simplified gyral pattern": [ + "HP:0009879" + ], + "cortical gyral simplification": [ + "HP:0009879" + ], + "broad distal phalanx of all finger": [ + "HP:0009880" + ], + "broad distal phalanges of all fingers": [ + "HP:0009880" + ], + "broad outermost hand bone": [ + "HP:0009880" + ], + "broad outermost hand bones": [ + "HP:0009880" + ], + "aplasia of the distal phalanx of the hand": [ + "HP:0009881" + ], + "aplasia of the distal phalanges of the hand": [ + "HP:0009881" + ], + "absent distal phalanx of the hand": [ + "HP:0009881" + ], + "absent distal phalanges of the hand": [ + "HP:0009881" + ], + "absent outermost hand bone": [ + "HP:0009881" + ], + "aplasia of outermost hand bone": [ + "HP:0009881" + ], + "short distal phalanx of finger": [ + "HP:0009882" + ], + "brachytelophalangy": [ + "HP:0009882" + ], + "distal phalangeal hypoplasia": [ + "HP:0009882" + ], + "hypoplasia of the distal phalanx": [ + "HP:0009882" + ], + "hypoplasia of the distal phalanges": [ + "HP:0009882" + ], + "hypoplasia of the distal phalanx of the hand": [ + "HP:0009882" + ], + "hypoplasia of the distal phalanges of the hand": [ + "HP:0009882" + ], + "hypoplasic terminal phalanx": [ + "HP:0009882" + ], + "hypoplasic terminal phalanges": [ + "HP:0009882" + ], + "hypoplastic distal phalanx": [ + "HP:0009882" + ], + "hypoplastic distal phalanges": [ + "HP:0009882" + ], + "hypoplastic terminal phalanx": [ + "HP:0009882" + ], + "hypoplastic terminal phalanges": [ + "HP:0009882" + ], + "short distal phalanx": [ + "HP:0009882" + ], + "short distal phalanges": [ + "HP:0009882" + ], + "short outermost finger bone": [ + "HP:0009882" + ], + "terminal phalangeal hypoplasia of hand": [ + "HP:0009882" + ], + "duplication of the distal phalanx of hand": [ + "HP:0009883" + ], + "bifid terminal phalanx": [ + "HP:0009883" + ], + "bifid terminal phalanges": [ + "HP:0009883" + ], + "duplication of the outermost bone of hand": [ + "HP:0009883" + ], + "notch outermost bone of hand": [ + "HP:0009883" + ], + "notched outermost bone of hand": [ + "HP:0009883" + ], + "partial / complete duplication of the distal phalanx of the hand": [ + "HP:0009883" + ], + "partial / complete duplication of the distal phalanges of the hand": [ + "HP:0009883" + ], + "taper distal phalanx of finger": [ + "HP:0009884" + ], + "tapered distal phalanges of finger": [ + "HP:0009884" + ], + "taper distal phalanx": [ + "HP:0009884" + ], + "tapered distal phalanges": [ + "HP:0009884" + ], + "taper distal phalanx of the hand": [ + "HP:0009884" + ], + "tapered distal phalanges of the hand": [ + "HP:0009884" + ], + "taper outermost finger bone": [ + "HP:0009884" + ], + "tapered outermost finger bone": [ + "HP:0009884" + ], + "obsolete prenatal short stature": [ + "HP:0009885" + ], + "trichorrhexis nodosa": [ + "HP:0009886" + ], + "abnormality of hair pigmentation": [ + "HP:0009887" + ], + "abnormality of hair color": [ + "HP:0009887" + ], + "abnormality of hair colour": [ + "HP:0009887" + ], + "abnormality of secondary sexual hair": [ + "HP:0009888" + ], + "localize hirsutism": [ + "HP:0009889" + ], + "localized hirsutism": [ + "HP:0009889" + ], + "localise abnormal hair growth": [ + "HP:0009889" + ], + "localised abnormal hair growth": [ + "HP:0009889" + ], + "localise hirsutism": [ + "HP:0009889" + ], + "localised hirsutism": [ + "HP:0009889" + ], + "localize abnormal hair growth": [ + "HP:0009889" + ], + "localized abnormal hair growth": [ + "HP:0009889" + ], + "high anterior hairline": [ + "HP:0009890" + ], + "high frontal hairline": [ + "HP:0009890" + ], + "underdeveloped supraorbital ridge": [ + "HP:0009891" + ], + "underdeveloped supraorbital ridges": [ + "HP:0009891" + ], + "depressed supraorbital margin": [ + "HP:0009891" + ], + "depressed supraorbital margins": [ + "HP:0009891" + ], + "depressed supraorbital ridge": [ + "HP:0009891" + ], + "flat supraorbital margin": [ + "HP:0009891" + ], + "flat supraorbital margins": [ + "HP:0009891" + ], + "flat supraorbital ridge": [ + "HP:0009891" + ], + "flatten bony protrusion above eye": [ + "HP:0009891" + ], + "flattened bony protrusion above eyes": [ + "HP:0009891" + ], + "hypoplasia of supraorbital margin": [ + "HP:0009891" + ], + "hypoplasia of supraorbital margins": [ + "HP:0009891" + ], + "hypoplasia of the supraorbital ridge": [ + "HP:0009891" + ], + "hypoplasia of the supraorbital ridges": [ + "HP:0009891" + ], + "hypoplastic supraorbital ridge": [ + "HP:0009891" + ], + "hypoplastic supraorbital ridges": [ + "HP:0009891" + ], + "shallow orbital ridge": [ + "HP:0009891" + ], + "shallow orbital ridges": [ + "HP:0009891" + ], + "shallow supraorbital ridge": [ + "HP:0009891" + ], + "underdeveloped brow": [ + "HP:0009891" + ], + "underdeveloped brows": [ + "HP:0009891" + ], + "anotia": [ + "HP:0009892" + ], + "absent ear": [ + "HP:0009892" + ], + "absent ears": [ + "HP:0009892" + ], + "congenital absence of external ear": [ + "HP:0009892" + ], + "telangiectasia of the ear": [ + "HP:0009893" + ], + "thickened ear": [ + "HP:0009894" + ], + "thickened ears": [ + "HP:0009894" + ], + "abnormality of the crus of the helix": [ + "HP:0009895" + ], + "abnormality of the crus of the ear": [ + "HP:0009895" + ], + "abnormality of the antitragus": [ + "HP:0009896" + ], + "horizontal crus of helix": [ + "HP:0009897" + ], + "helix , crus , horizontal": [ + "HP:0009897" + ], + "horizontal orientation of the crus of helix": [ + "HP:0009897" + ], + "horizontal orientation of the ear crus": [ + "HP:0009897" + ], + "railroad track ear": [ + "HP:0009897" + ], + "railroad track ears": [ + "HP:0009897" + ], + "railroad track sign": [ + "HP:0009897" + ], + "underdeveloped crus of the helix": [ + "HP:0009898" + ], + "hypoplasia of the crus of the ear": [ + "HP:0009898" + ], + "underdeveloped crus of the ear": [ + "HP:0009898" + ], + "prominent crus of helix": [ + "HP:0009899" + ], + "abnormal prominence of the crus of the ear": [ + "HP:0009899" + ], + "helix , crus , prominent": [ + "HP:0009899" + ], + "hyperplastic helix crus": [ + "HP:0009899" + ], + "hypertrophic helix crus": [ + "HP:0009899" + ], + "unilateral deafness": [ + "HP:0009900" + ], + "deafness in one ear": [ + "HP:0009900" + ], + "deafness , unilateral": [ + "HP:0009900" + ], + "crumple ear": [ + "HP:0009901" + ], + "crumpled ear": [ + "HP:0009901" + ], + "cleft helix": [ + "HP:0009902" + ], + "notch helix": [ + "HP:0009902" + ], + "notched helix": [ + "HP:0009902" + ], + "notching of the ear helix": [ + "HP:0009902" + ], + "conjunctival nodule": [ + "HP:0009903" + ], + "prominent ear helix": [ + "HP:0009904" + ], + "large helix": [ + "HP:0009904" + ], + "thin ear helix": [ + "HP:0009905" + ], + "aplasia / hypoplasia of the earlobe": [ + "HP:0009906" + ], + "aplasia / hypoplasia of the earlobes": [ + "HP:0009906" + ], + "absent / small ear lobe": [ + "HP:0009906" + ], + "absent / small ear lobes": [ + "HP:0009906" + ], + "absent / underdevelop ear lobe": [ + "HP:0009906" + ], + "absent / underdeveloped ear lobes": [ + "HP:0009906" + ], + "attach earlobe": [ + "HP:0009907" + ], + "attached earlobe": [ + "HP:0009907" + ], + "adherent earlobe": [ + "HP:0009907" + ], + "anterior crease of earlobe": [ + "HP:0009908" + ], + "anterior creases of earlobe": [ + "HP:0009908" + ], + "earlobe crease": [ + "HP:0009908" + ], + "transverse earlobe crease": [ + "HP:0009908" + ], + "transverse earlobe creases": [ + "HP:0009908" + ], + "uplifted earlobe": [ + "HP:0009909" + ], + "fleshy upturned lobule": [ + "HP:0009909" + ], + "fleshy upturned lobules": [ + "HP:0009909" + ], + "lobe , uplift": [ + "HP:0009909" + ], + "lobe , uplifted": [ + "HP:0009909" + ], + "uplifted earlobes": [ + "HP:0009909" + ], + "upturned earlobe": [ + "HP:0009909" + ], + "upturned earlobes": [ + "HP:0009909" + ], + "aplasia of the middle ear ossicle": [ + "HP:0009910" + ], + "aplasia of the middle ear ossicles": [ + "HP:0009910" + ], + "absent middle ear bone": [ + "HP:0009910" + ], + "absent middle ear bones": [ + "HP:0009910" + ], + "absent middle ear ossicle": [ + "HP:0009910" + ], + "absent middle ear ossicles": [ + "HP:0009910" + ], + "abnormal temporal bone morphology": [ + "HP:0009911" + ], + "abnormality of the temporal bone": [ + "HP:0009911" + ], + "abnormality of the tragus": [ + "HP:0009912" + ], + "aplasia / hypoplasia of the tragus": [ + "HP:0009913" + ], + "absent / small tragus": [ + "HP:0009913" + ], + "absent / underdevelop tragus": [ + "HP:0009913" + ], + "absent / underdeveloped tragus": [ + "HP:0009913" + ], + "cyclopia": [ + "HP:0009914" + ], + "cyclops eye": [ + "HP:0009914" + ], + "single central eye": [ + "HP:0009914" + ], + "corneal asymmetry": [ + "HP:0009915" + ], + "asymmetry of the cornea": [ + "HP:0009915" + ], + "asymmetry of the corneas": [ + "HP:0009915" + ], + "anisocoria": [ + "HP:0009916" + ], + "asymmetric pupil size": [ + "HP:0009916" + ], + "asymmetric pupil sizes": [ + "HP:0009916" + ], + "asymmetry of the pupil": [ + "HP:0009916" + ], + "asymmetry of the pupils": [ + "HP:0009916" + ], + "unequal pupil dilatation": [ + "HP:0009916" + ], + "unequal pupil size": [ + "HP:0009916" + ], + "persistent pupillary membrane": [ + "HP:0009917" + ], + "ectopia pupillae": [ + "HP:0009918" + ], + "corectopia": [ + "HP:0009918" + ], + "displace pupil": [ + "HP:0009918" + ], + "displaced pupil": [ + "HP:0009918" + ], + "retinoblastoma": [ + "HP:0009919" + ], + "retina tumor": [ + "HP:0009919" + ], + "retina tumour": [ + "HP:0009919" + ], + "nevus of ota": [ + "HP:0009920" + ], + "congenital melanosis bulbi": [ + "HP:0009920" + ], + "naevus fuscoceruleus ophthalmomaxillaris": [ + "HP:0009920" + ], + "nevus fuscoceruleus ophthalmomaxillaris": [ + "HP:0009920" + ], + "oculodermal melanocytosis": [ + "HP:0009920" + ], + "duane anomaly": [ + "HP:0009921" + ], + "globe retraction and deviation on adduction": [ + "HP:0009921" + ], + "limited eye motility from duane anomaly": [ + "HP:0009921" + ], + "limited eye movement from duane anomaly": [ + "HP:0009921" + ], + "vascular remnant arise from the disc": [ + "HP:0009922" + ], + "vascular remnant arising from the disc": [ + "HP:0009922" + ], + "persistence of the hyaloid artery": [ + "HP:0009922" + ], + "persistent hyaloid artery": [ + "HP:0009922" + ], + "aplasia / hypoplasia involve the nose": [ + "HP:0009924" + ], + "aplasia / hypoplasia involving the nose": [ + "HP:0009924" + ], + "decrease nasal size": [ + "HP:0009924" + ], + "decreased nasal size": [ + "HP:0009924" + ], + "decreased size of nose": [ + "HP:0009924" + ], + "hypoplasia of the nose": [ + "HP:0009924" + ], + "hypotrophic nose": [ + "HP:0009924" + ], + "epiphora": [ + "HP:0009926" + ], + "increase lacrimation": [ + "HP:0009926" + ], + "increased lacrimation": [ + "HP:0009926" + ], + "increase tear": [ + "HP:0009926" + ], + "increased tears": [ + "HP:0009926" + ], + "tear": [ + "HP:0009926" + ], + "tearing": [ + "HP:0009926" + ], + "watery eye": [ + "HP:0009926" + ], + "watery eyes": [ + "HP:0009926" + ], + "aplasia of the nose": [ + "HP:0009927" + ], + "absent nose": [ + "HP:0009927" + ], + "arrhinia": [ + "HP:0009927" + ], + "failure of development of nose": [ + "HP:0009927" + ], + "miss nose": [ + "HP:0009927" + ], + "missing nose": [ + "HP:0009927" + ], + "nasal underdevelopment": [ + "HP:0009927" + ], + "underdevelopment of nose": [ + "HP:0009927" + ], + "thick nasal ala": [ + "HP:0009928" + ], + "thick nasal alae": [ + "HP:0009928" + ], + "ala nasi , thick": [ + "HP:0009928" + ], + "thickening of the ala nasi": [ + "HP:0009928" + ], + "thickening of the alae nasi": [ + "HP:0009928" + ], + "abnormality of the columella": [ + "HP:0009929" + ], + "anomaly of the columella": [ + "HP:0009929" + ], + "deformity of the columella": [ + "HP:0009929" + ], + "malformation of the columella": [ + "HP:0009929" + ], + "asymmetry of the naris": [ + "HP:0009930" + ], + "asymmetry of the nares": [ + "HP:0009930" + ], + "asymmetry of nostril": [ + "HP:0009930" + ], + "asymmetry of nostrils": [ + "HP:0009930" + ], + "crook nostril": [ + "HP:0009930" + ], + "crooked nostrils": [ + "HP:0009930" + ], + "unequal nostril shape": [ + "HP:0009930" + ], + "unequal nostril size": [ + "HP:0009930" + ], + "uneven nostril shape": [ + "HP:0009930" + ], + "uneven nostril size": [ + "HP:0009930" + ], + "enlarge naris": [ + "HP:0009931" + ], + "enlarged naris": [ + "HP:0009931" + ], + "broad nostril": [ + "HP:0009931" + ], + "dilate naris": [ + "HP:0009931" + ], + "dilated nares": [ + "HP:0009931" + ], + "dilate nostril": [ + "HP:0009931" + ], + "dilated nostril": [ + "HP:0009931" + ], + "enlarged nares": [ + "HP:0009931" + ], + "enlarge nostril": [ + "HP:0009931" + ], + "enlarged nostril": [ + "HP:0009931" + ], + "increase diameter of naris": [ + "HP:0009931" + ], + "increased diameter of nares": [ + "HP:0009931" + ], + "increase diameter of nostril": [ + "HP:0009931" + ], + "increased diameter of nostril": [ + "HP:0009931" + ], + "increase width of naris": [ + "HP:0009931" + ], + "increased width of nares": [ + "HP:0009931" + ], + "large naris": [ + "HP:0009931" + ], + "large nares": [ + "HP:0009931" + ], + "naris , broad": [ + "HP:0009931" + ], + "naris , enlarge": [ + "HP:0009931" + ], + "naris , enlarged": [ + "HP:0009931" + ], + "wide naris": [ + "HP:0009931" + ], + "wide nares": [ + "HP:0009931" + ], + "wide nostril": [ + "HP:0009931" + ], + "single naris": [ + "HP:0009932" + ], + "mono nostril": [ + "HP:0009932" + ], + "one nostril": [ + "HP:0009932" + ], + "single nare": [ + "HP:0009932" + ], + "single nostril": [ + "HP:0009932" + ], + "narrow naris": [ + "HP:0009933" + ], + "collapse nostril": [ + "HP:0009933" + ], + "collapsed nostrils": [ + "HP:0009933" + ], + "naris , narrow": [ + "HP:0009933" + ], + "naris , slit - like": [ + "HP:0009933" + ], + "narrow nares": [ + "HP:0009933" + ], + "narrow nostril": [ + "HP:0009933" + ], + "narrow nostrils": [ + "HP:0009933" + ], + "slit - like nostril": [ + "HP:0009933" + ], + "slit - like nostrils": [ + "HP:0009933" + ], + "small nostril": [ + "HP:0009933" + ], + "small nostrils": [ + "HP:0009933" + ], + "thin naris": [ + "HP:0009933" + ], + "thin nares": [ + "HP:0009933" + ], + "thin nostril": [ + "HP:0009933" + ], + "thin nostrils": [ + "HP:0009933" + ], + "supernumerary naris": [ + "HP:0009934" + ], + "accessory naris": [ + "HP:0009934" + ], + "accessory nares": [ + "HP:0009934" + ], + "accessory nostril": [ + "HP:0009934" + ], + "extra nostril": [ + "HP:0009934" + ], + "supernumerary nares": [ + "HP:0009934" + ], + "supernumerary nostril": [ + "HP:0009934" + ], + "supernumerary nostrils": [ + "HP:0009934" + ], + "aplasia / hypoplasia of the nasal septum": [ + "HP:0009935" + ], + "ageneis of nasal septum": [ + "HP:0009935" + ], + "failure of development of nasal septum": [ + "HP:0009935" + ], + "underdevelopment of nasal septum": [ + "HP:0009935" + ], + "narrow nasal septum": [ + "HP:0009936" + ], + "decrease width of nasal septum": [ + "HP:0009936" + ], + "decreased width of nasal septum": [ + "HP:0009936" + ], + "narrow septum of nose": [ + "HP:0009936" + ], + "thin nasal septum": [ + "HP:0009936" + ], + "thin septum of nose": [ + "HP:0009936" + ], + "facial hirsutism": [ + "HP:0009937" + ], + "excessive face hair": [ + "HP:0009937" + ], + "sunken cheek": [ + "HP:0009938" + ], + "sunken cheeks": [ + "HP:0009938" + ], + "depressed cheek": [ + "HP:0009938" + ], + "depressed cheeks": [ + "HP:0009938" + ], + "hollow cheek": [ + "HP:0009938" + ], + "hollow cheeks": [ + "HP:0009938" + ], + "mandibular aplasia": [ + "HP:0009939" + ], + "absence of low jaw": [ + "HP:0009939" + ], + "absence of lower jaw": [ + "HP:0009939" + ], + "absence of low jaw bone": [ + "HP:0009939" + ], + "absence of lower jaw bone": [ + "HP:0009939" + ], + "absence of lower jaw bones": [ + "HP:0009939" + ], + "absence of mandible": [ + "HP:0009939" + ], + "absent mandible": [ + "HP:0009939" + ], + "agenesis of the mandible": [ + "HP:0009939" + ], + "agnathia": [ + "HP:0009939" + ], + "aplasia of the low jaw bone": [ + "HP:0009939" + ], + "aplasia of the lower jaw bone": [ + "HP:0009939" + ], + "failure of development of low jaw": [ + "HP:0009939" + ], + "failure of development of lower jaw": [ + "HP:0009939" + ], + "failure of development of mandible": [ + "HP:0009939" + ], + "miss low jaw": [ + "HP:0009939" + ], + "missing lower jaw": [ + "HP:0009939" + ], + "asymmetry of the mandible": [ + "HP:0009940" + ], + "asymmetry of low jaw": [ + "HP:0009940" + ], + "asymmetry of lower jaw": [ + "HP:0009940" + ], + "cant low jaw": [ + "HP:0009940" + ], + "canted lower jaw": [ + "HP:0009940" + ], + "cant mandible": [ + "HP:0009940" + ], + "canted mandible": [ + "HP:0009940" + ], + "crook low jaw": [ + "HP:0009940" + ], + "crooked lower jaw": [ + "HP:0009940" + ], + "deviation of low jaw": [ + "HP:0009940" + ], + "deviation of lower jaw": [ + "HP:0009940" + ], + "deviation of mandible": [ + "HP:0009940" + ], + "deviation of the low jaw": [ + "HP:0009940" + ], + "deviation of the lower jaw": [ + "HP:0009940" + ], + "deviation of the mandible": [ + "HP:0009940" + ], + "low jaw shift to one side": [ + "HP:0009940" + ], + "lower jaw shifted to one side": [ + "HP:0009940" + ], + "tilt low jaw": [ + "HP:0009940" + ], + "tilted lower jaw": [ + "HP:0009940" + ], + "tilt mandible": [ + "HP:0009940" + ], + "tilted mandible": [ + "HP:0009940" + ], + "uneven low jaw": [ + "HP:0009940" + ], + "uneven lower jaw": [ + "HP:0009940" + ], + "uneven mandible": [ + "HP:0009940" + ], + "asymmetry of the mouth": [ + "HP:0009941" + ], + "asymmetry of oral cavity": [ + "HP:0009941" + ], + "cant mouth": [ + "HP:0009941" + ], + "canted mouth": [ + "HP:0009941" + ], + "crook mouth": [ + "HP:0009941" + ], + "crooked mouth": [ + "HP:0009941" + ], + "tilt mouth": [ + "HP:0009941" + ], + "tilted mouth": [ + "HP:0009941" + ], + "uneven mouth": [ + "HP:0009941" + ], + "duplication of thumb phalanx": [ + "HP:0009942" + ], + "complete / partial duplication of phalanx of the thumb": [ + "HP:0009942" + ], + "complete / partial duplication of phalanges of the thumb": [ + "HP:0009942" + ], + "duplicate thumb": [ + "HP:0009942" + ], + "duplicated thumb": [ + "HP:0009942" + ], + "duplicated thumbs": [ + "HP:0009942" + ], + "duplication of phalanx of thumb": [ + "HP:0009942" + ], + "complete duplication of thumb phalanx": [ + "HP:0009943" + ], + "complete duplication of the phalanx of the thumb": [ + "HP:0009943" + ], + "complete duplication of the phalanges of the thumb": [ + "HP:0009943" + ], + "complete duplication of thumb bone": [ + "HP:0009943" + ], + "complete duplication of thumb bones": [ + "HP:0009943" + ], + "digitalization of thumb": [ + "HP:0009943" + ], + "digitalization of thumbs": [ + "HP:0009943" + ], + "partial duplication of thumb phalanx": [ + "HP:0009944" + ], + "bifid thumb": [ + "HP:0009944" + ], + "notching of thumb phalanx": [ + "HP:0009944" + ], + "notching of thumb phalanges": [ + "HP:0009944" + ], + "partial duplication of the phalanx of the thumb": [ + "HP:0009944" + ], + "partial duplication of the phalanges of the thumb": [ + "HP:0009944" + ], + "partial duplication of the thumb bone": [ + "HP:0009944" + ], + "partial duplication of the thumb bones": [ + "HP:0009944" + ], + "duplication of phalanx of 2nd finger": [ + "HP:0009945" + ], + "duplication of the bone of index finger": [ + "HP:0009945" + ], + "duplication of the bones of index finger": [ + "HP:0009945" + ], + "partial / complete duplication of phalanx of the 2nd finger": [ + "HP:0009945" + ], + "partial / complete duplication of phalanges of the 2nd finger": [ + "HP:0009945" + ], + "polydactyly affect the 2nd finger": [ + "HP:0009946" + ], + "polydactyly affecting the 2nd finger": [ + "HP:0009946" + ], + "extra index finger": [ + "HP:0009946" + ], + "duplication of the proximal phalanx of the 2nd finger": [ + "HP:0009947" + ], + "duplication of the proximal bone of the index finger": [ + "HP:0009947" + ], + "duplication of the proximal bones of the index finger": [ + "HP:0009947" + ], + "partial / complete duplication of the proximal phalanx of the 2nd finger": [ + "HP:0009947" + ], + "duplication of the distal phalanx of the 2nd finger": [ + "HP:0009948" + ], + "partial / complete duplication of the distal phalanx of the 2nd finger": [ + "HP:0009948" + ], + "partial / complete duplication of the outermost bone of the index finger": [ + "HP:0009948" + ], + "duplication of the middle phalanx of the 2nd finger": [ + "HP:0009949" + ], + "partial / complete duplication of the middle bone of the index finger": [ + "HP:0009949" + ], + "partial / complete duplication of the middle bones of the index finger": [ + "HP:0009949" + ], + "partial / complete duplication of the middle phalanx of the 2nd finger": [ + "HP:0009949" + ], + "complete duplication of the distal phalanx of the 2nd finger": [ + "HP:0009950" + ], + "complete duplication of the outermost bone of the index finger": [ + "HP:0009950" + ], + "partial duplication of the distal phalanx of the 2nd finger": [ + "HP:0009951" + ], + "bifid terminal phalanx of the 2nd finger": [ + "HP:0009951" + ], + "notch outermost bone of the index finger": [ + "HP:0009951" + ], + "notched outermost bone of the index finger": [ + "HP:0009951" + ], + "partial duplication of the outermost bone of the 2nd finger": [ + "HP:0009951" + ], + "complete duplication of the middle phalanx of the 2nd finger": [ + "HP:0009952" + ], + "complete duplication of the middle bone of the index finger": [ + "HP:0009952" + ], + "partial duplication of the middle phalanx of the 2nd finger": [ + "HP:0009953" + ], + "partial duplication of the middle bone of the index finger": [ + "HP:0009953" + ], + "complete duplication of the proximal phalanx of the 2nd finger": [ + "HP:0009954" + ], + "complete duplication of the proximal bone of the index finger": [ + "HP:0009954" + ], + "partial duplication of the proximal phalanx of the 2nd finger": [ + "HP:0009955" + ], + "partial duplication of the proximal bone of the index finger": [ + "HP:0009955" + ], + "partial duplication of the proximal bones of the index finger": [ + "HP:0009955" + ], + "partial duplication of the phalanx of the 2nd finger": [ + "HP:0009956" + ], + "partial duplication of the phalanges of the 2nd finger": [ + "HP:0009956" + ], + "partial duplication of the bone of the index finger": [ + "HP:0009956" + ], + "partial duplication of the bones of the index finger": [ + "HP:0009956" + ], + "complete duplication of the phalanx of the 2nd finger": [ + "HP:0009957" + ], + "complete duplication of the phalanges of the 2nd finger": [ + "HP:0009957" + ], + "complete duplication of the bone of the index finger": [ + "HP:0009957" + ], + "complete duplication of the bones of the index finger": [ + "HP:0009957" + ], + "polydactyly affect the 3rd finger": [ + "HP:0009958" + ], + "polydactyly affecting the 3rd finger": [ + "HP:0009958" + ], + "extra middle finger": [ + "HP:0009958" + ], + "duplication of phalanx of 3rd finger": [ + "HP:0009959" + ], + "duplication of middle finger bone": [ + "HP:0009959" + ], + "partial / complete duplication of phalanx of the 3rd finger": [ + "HP:0009959" + ], + "partial / complete duplication of phalanges of the 3rd finger": [ + "HP:0009959" + ], + "complete duplication of the phalanx of the 3rd finger": [ + "HP:0009960" + ], + "complete duplication of the phalanges of the 3rd finger": [ + "HP:0009960" + ], + "complete duplication of middle finger bone": [ + "HP:0009960" + ], + "complete duplication of middle finger bones": [ + "HP:0009960" + ], + "partial duplication of the phalanx of the 3rd finger": [ + "HP:0009961" + ], + "partial duplication of the phalanges of the 3rd finger": [ + "HP:0009961" + ], + "partial duplication of middle finger bone": [ + "HP:0009961" + ], + "partial duplication of middle finger bones": [ + "HP:0009961" + ], + "duplication of the distal phalanx of the 3rd finger": [ + "HP:0009962" + ], + "partial / complete duplication of the distal phalanx of the 3rd finger": [ + "HP:0009962" + ], + "partial / complete duplication of the outermost bone of the middle finger": [ + "HP:0009962" + ], + "duplication of the middle phalanx of the 3rd finger": [ + "HP:0009963" + ], + "duplication of the middle bone of the middle finger": [ + "HP:0009963" + ], + "partial / complete duplication of the middle phalanx of the 3rd finger": [ + "HP:0009963" + ], + "duplication of the proximal phalanx of the 3rd finger": [ + "HP:0009964" + ], + "duplication of the proximal bone of the middle finger": [ + "HP:0009964" + ], + "partial / complete duplication of the proximal phalanx of the 3rd finger": [ + "HP:0009964" + ], + "complete duplication of the distal phalanx of the 3rd finger": [ + "HP:0009965" + ], + "complete duplication of the outermost bone of the 3rd finger": [ + "HP:0009965" + ], + "complete duplication of the middle phalanx of the 3rd finger": [ + "HP:0009966" + ], + "complete duplication of the middle bone of the middle finger": [ + "HP:0009966" + ], + "complete duplication of the proximal phalanx of the 3rd finger": [ + "HP:0009967" + ], + "complete duplication of the innermost bone of the 3rd finger": [ + "HP:0009967" + ], + "partial duplication of the distal phalanx of the 3rd finger": [ + "HP:0009968" + ], + "bifid terminal phalanx of the 3rd finger": [ + "HP:0009968" + ], + "notch outermost bone of the middle finger": [ + "HP:0009968" + ], + "notched outermost bone of the middle finger": [ + "HP:0009968" + ], + "partial duplication of the outermost bone of the middle finger": [ + "HP:0009968" + ], + "partial duplication of the middle phalanx of the 3rd finger": [ + "HP:0009969" + ], + "partial duplication of the middle bone of the 3rd finger": [ + "HP:0009969" + ], + "partial duplication of the proximal phalanx of the 3rd finger": [ + "HP:0009970" + ], + "partial duplication of the proximal bone of the middle finger": [ + "HP:0009970" + ], + "polydactyly affect the 4th finger": [ + "HP:0009971" + ], + "polydactyly affecting the 4th finger": [ + "HP:0009971" + ], + "extra ring finger": [ + "HP:0009971" + ], + "duplication of phalanx of 4th finger": [ + "HP:0009972" + ], + "duplication of bone of the ring finger": [ + "HP:0009972" + ], + "duplication of bones of the ring finger": [ + "HP:0009972" + ], + "partial / complete duplication of phalanx of the 4th finger": [ + "HP:0009972" + ], + "partial / complete duplication of phalanges of the 4th finger": [ + "HP:0009972" + ], + "complete duplication of the phalanx of the 4th finger": [ + "HP:0009973" + ], + "complete duplication of the phalanges of the 4th finger": [ + "HP:0009973" + ], + "complete duplication of the bone of the ring finger": [ + "HP:0009973" + ], + "complete duplication of the bones of the ring finger": [ + "HP:0009973" + ], + "partial duplication of the phalanx of the 4th finger": [ + "HP:0009974" + ], + "partial duplication of the phalanges of the 4th finger": [ + "HP:0009974" + ], + "partial duplication of the bone of the ring finger": [ + "HP:0009974" + ], + "partial duplication of the bones of the ring finger": [ + "HP:0009974" + ], + "duplication of the distal phalanx of the 4th finger": [ + "HP:0009975" + ], + "partial / complete duplication of the distal phalanx of the 4th finger": [ + "HP:0009975" + ], + "partial / complete duplication of the outermost bone of the ring finger": [ + "HP:0009975" + ], + "duplication of the middle phalanx of the 4th finger": [ + "HP:0009976" + ], + "partial / complete duplication of the middle bone of the ring finger": [ + "HP:0009976" + ], + "partial / complete duplication of the middle phalanx of the 4th finger": [ + "HP:0009976" + ], + "duplication of the proximal phalanx of the 4th finger": [ + "HP:0009977" + ], + "duplication of the proximal bone of the ring finger": [ + "HP:0009977" + ], + "partial / complete duplication of the proximal phalanx of the 4th finger": [ + "HP:0009977" + ], + "complete duplication of the distal phalanx of the 4th finger": [ + "HP:0009978" + ], + "complete duplication of the outermost bone of the ring finger": [ + "HP:0009978" + ], + "complete duplication of the middle phalanx of the 4th finger": [ + "HP:0009979" + ], + "complete duplication of the middle bone of the ring finger": [ + "HP:0009979" + ], + "complete duplication of the proximal phalanx of the 4th finger": [ + "HP:0009980" + ], + "complete duplication of the proximal bone of the ring finger": [ + "HP:0009980" + ], + "partial duplication of the distal phalanx of the 4th finger": [ + "HP:0009981" + ], + "bifid terminal phalanx of the 4th finger": [ + "HP:0009981" + ], + "notch outermost bone of the ring finger": [ + "HP:0009981" + ], + "notched outermost bone of the ring finger": [ + "HP:0009981" + ], + "partial duplication of the outermost bone of the ring finger": [ + "HP:0009981" + ], + "partial duplication of the middle phalanx of the 4th finger": [ + "HP:0009982" + ], + "partial duplication of the middle bone of the ring finger": [ + "HP:0009982" + ], + "partial duplication of the proximal phalanx of the 4th finger": [ + "HP:0009983" + ], + "partial duplication of the innermost bone of the ring finger": [ + "HP:0009983" + ], + "duplication of phalanx of 5th finger": [ + "HP:0009985" + ], + "partial / complete duplication of little finger bone": [ + "HP:0009985" + ], + "partial / complete duplication of phalanx of the 5th finger": [ + "HP:0009985" + ], + "partial / complete duplication of phalanges of the 5th finger": [ + "HP:0009985" + ], + "partial / complete duplication of pinkie finger bone": [ + "HP:0009985" + ], + "partial / complete duplication of pinky finger bone": [ + "HP:0009985" + ], + "complete duplication of the phalanx of the 5th finger": [ + "HP:0009986" + ], + "complete duplication of the phalanges of the 5th finger": [ + "HP:0009986" + ], + "complete duplication of the little finger bone": [ + "HP:0009986" + ], + "complete duplication of the pinkie finger bone": [ + "HP:0009986" + ], + "complete duplication of the pinky finger bone": [ + "HP:0009986" + ], + "partial duplication of the phalanx of the 5th finger": [ + "HP:0009987" + ], + "partial duplication of the phalanges of the 5th finger": [ + "HP:0009987" + ], + "partial duplication of the little finger bone": [ + "HP:0009987" + ], + "partial duplication of the pinkie finger bone": [ + "HP:0009987" + ], + "partial duplication of the pinky finger bone": [ + "HP:0009987" + ], + "duplication of the distal phalanx of the 5th finger": [ + "HP:0009988" + ], + "duplication of the outermost little finger bone": [ + "HP:0009988" + ], + "duplication of the outermost pinkie finger bone": [ + "HP:0009988" + ], + "duplication of the outermost pinky finger bone": [ + "HP:0009988" + ], + "partial / complete duplication of the distal phalanx of the 5th finger": [ + "HP:0009988" + ], + "duplication of the middle phalanx of the 5th finger": [ + "HP:0009989" + ], + "duplication of the middle little finger bone": [ + "HP:0009989" + ], + "duplication of the middle pinkie finger bone": [ + "HP:0009989" + ], + "duplication of the middle pinky finger bone": [ + "HP:0009989" + ], + "partial / complete duplication of the middle phalanx of the 5th finger": [ + "HP:0009989" + ], + "duplication of the proximal phalanx of the 5th finger": [ + "HP:0009990" + ], + "duplication of the innermost little finger bone": [ + "HP:0009990" + ], + "duplication of the innermost pinkie finger bone": [ + "HP:0009990" + ], + "duplication of the innermost pinky finger bone": [ + "HP:0009990" + ], + "partial / complete duplication of the proximal phalanx of the 5th finger": [ + "HP:0009990" + ], + "complete duplication of the distal phalanx of the 5th finger": [ + "HP:0009991" + ], + "complete duplication of the outermost little finger bone": [ + "HP:0009991" + ], + "complete duplication of the outermost pinkie finger bone": [ + "HP:0009991" + ], + "complete duplication of the outermost pinky finger bone": [ + "HP:0009991" + ], + "complete duplication of the middle phalanx of the 5th finger": [ + "HP:0009992" + ], + "complete duplication of the middle little finger bone": [ + "HP:0009992" + ], + "complete duplication of the middle pinkie finger bone": [ + "HP:0009992" + ], + "complete duplication of the middle pinky finger bone": [ + "HP:0009992" + ], + "complete duplication of the proximal phalanx of the 5th finger": [ + "HP:0009993" + ], + "complete duplication of the innermost little finger bone": [ + "HP:0009993" + ], + "complete duplication of the innermost pinkie finger bone": [ + "HP:0009993" + ], + "complete duplication of the innermost pinky finger bone": [ + "HP:0009993" + ], + "partial duplication of the distal phalanx of the 5th finger": [ + "HP:0009994" + ], + "bifid terminal phalanx of the 5th finger": [ + "HP:0009994" + ], + "notch outermost pinky finger bone": [ + "HP:0009994" + ], + "notched outermost pinky finger bone": [ + "HP:0009994" + ], + "partial duplication of outermost little finger bone": [ + "HP:0009994" + ], + "partial duplication of outermost pinkie finger bone": [ + "HP:0009994" + ], + "partial duplication of outermost pinky finger bone": [ + "HP:0009994" + ], + "partial duplication of the middle phalanx of the 5th finger": [ + "HP:0009995" + ], + "partial duplication of the middle little finger bone": [ + "HP:0009995" + ], + "partial duplication of the middle pinkie finger bone": [ + "HP:0009995" + ], + "partial duplication of the middle pinky finger bone": [ + "HP:0009995" + ], + "partial duplication of the proximal phalanx of the 5th finger": [ + "HP:0009996" + ], + "partial duplication of the innermost little finger bone": [ + "HP:0009996" + ], + "partial duplication of the innermost pinkie finger bone": [ + "HP:0009996" + ], + "partial duplication of the innermost pinky finger bone": [ + "HP:0009996" + ], + "duplication of phalanx of hand": [ + "HP:0009997" + ], + "duplication of finger bone": [ + "HP:0009997" + ], + "duplication of finger bones": [ + "HP:0009997" + ], + "complete duplication of phalanx of hand": [ + "HP:0009998" + ], + "complete duplication of hand bone": [ + "HP:0009998" + ], + "complete duplication of hand bones": [ + "HP:0009998" + ], + "partial duplication of the phalanx of hand": [ + "HP:0009999" + ], + "partial duplication of hand bone": [ + "HP:0009999" + ], + "partial duplication of hand bones": [ + "HP:0009999" + ], + "complete duplication of the proximal phalanx of the hand": [ + "HP:0010000" + ], + "complete duplication of the proximal phalanges of the hand": [ + "HP:0010000" + ], + "complete duplication of the innermost bone of the hand": [ + "HP:0010000" + ], + "complete duplication of the innermost bones of the hand": [ + "HP:0010000" + ], + "complete duplication of the distal phalanx of the hand": [ + "HP:0010001" + ], + "complete duplication of the distal phalanges of the hand": [ + "HP:0010001" + ], + "complete duplication of the outermost bone of the hand": [ + "HP:0010001" + ], + "complete duplication of the outermost bones of the hand": [ + "HP:0010001" + ], + "complete duplication of the middle phalanx of the hand": [ + "HP:0010002" + ], + "complete duplication of the middle phalanges of the hand": [ + "HP:0010002" + ], + "complete duplication of the middle bone of the hand": [ + "HP:0010002" + ], + "complete duplication of the middle bones of the hand": [ + "HP:0010002" + ], + "partial duplication of the proximal phalanx of the hand": [ + "HP:0010003" + ], + "partial duplication of the proximal phalanges of the hand": [ + "HP:0010003" + ], + "partial duplication of the innermost bone of the hand": [ + "HP:0010003" + ], + "partial duplication of the innermost bones of the hand": [ + "HP:0010003" + ], + "partial duplication of the distal phalanx of the hand": [ + "HP:0010004" + ], + "partial duplication of the distal phalanges of the hand": [ + "HP:0010004" + ], + "bifid terminal phalanx of the hand": [ + "HP:0010004" + ], + "bifid terminal phalanges of the hand": [ + "HP:0010004" + ], + "partial duplication of the outermost bone of the hand": [ + "HP:0010004" + ], + "partial duplication of the middle phalanx of the hand": [ + "HP:0010005" + ], + "partial duplication of the middle phalanges of the hand": [ + "HP:0010005" + ], + "partial duplication of the middle bone of hand": [ + "HP:0010005" + ], + "partial duplication of the middle bones of hand": [ + "HP:0010005" + ], + "duplication of the proximal phalanx of hand": [ + "HP:0010006" + ], + "duplication of the innermost bone of hand": [ + "HP:0010006" + ], + "duplication of the innermost bones of hand": [ + "HP:0010006" + ], + "partial / complete duplication of the proximal phalanx of the hand": [ + "HP:0010006" + ], + "partial / complete duplication of the proximal phalanges of the hand": [ + "HP:0010006" + ], + "duplication of the middle phalanx of hand": [ + "HP:0010008" + ], + "duplication of the middle bone of hand": [ + "HP:0010008" + ], + "duplication of the middle bones of hand": [ + "HP:0010008" + ], + "partial / complete duplication of the middle phalanx of the hand": [ + "HP:0010008" + ], + "partial / complete duplication of the middle phalanges of the hand": [ + "HP:0010008" + ], + "abnormality of the 1st metacarpal": [ + "HP:0010009" + ], + "abnormality of the 1st long bone of hand": [ + "HP:0010009" + ], + "abnormality of the 2nd metacarpal": [ + "HP:0010010" + ], + "abnormality of the 2nd long bone of hand": [ + "HP:0010010" + ], + "abnormality of the 3rd metacarpal": [ + "HP:0010011" + ], + "abnormality of the 3rd long bone of hand": [ + "HP:0010011" + ], + "abnormality of the 4th metacarpal": [ + "HP:0010012" + ], + "abnormality of the 4th long bone of hand": [ + "HP:0010012" + ], + "abnormality of the 5th metacarpal": [ + "HP:0010013" + ], + "abnormality of the 5th long bone of hand": [ + "HP:0010013" + ], + "abnormality of the epiphysis of the 1st metacarpal": [ + "HP:0010014" + ], + "abnormality of the end part of the 1st long bone of hand": [ + "HP:0010014" + ], + "absent epiphysis of the 1st metacarpal": [ + "HP:0010015" + ], + "absent end part of the 1st long bone of hand": [ + "HP:0010015" + ], + "bracket epiphysis of the 1st metacarpal": [ + "HP:0010016" + ], + "bracket shape end part of 1st long bone of hand": [ + "HP:0010016" + ], + "bracket shaped end part of 1st long bone of hand": [ + "HP:0010016" + ], + "cone - shaped epiphysis of the 1st metacarpal": [ + "HP:0010017" + ], + "cone - shaped end part of the 1st long bone of hand": [ + "HP:0010017" + ], + "enlarged epiphysis of the 1st metacarpal": [ + "HP:0010018" + ], + "enlarged end part of the 1st long bone of hand": [ + "HP:0010018" + ], + "fragmentation of the epiphysis of the 1st metacarpal": [ + "HP:0010019" + ], + "fragmentation of the end part of the 1st long bone of hand": [ + "HP:0010019" + ], + "irregular epiphysis of the 1st metacarpal": [ + "HP:0010020" + ], + "irregular end part of the 1st long bone of hand": [ + "HP:0010020" + ], + "ivory epiphysis of the 1st metacarpal": [ + "HP:0010021" + ], + "increase bone density of end part of the 1st long bone of hand": [ + "HP:0010021" + ], + "increased bone density of end part of the 1st long bone of hand": [ + "HP:0010021" + ], + "pseudoepiphysis of the 1st metacarpal": [ + "HP:0010022" + ], + "small epiphysis of the 1st metacarpal": [ + "HP:0010023" + ], + "small end part of the 1st long bone of hand": [ + "HP:0010023" + ], + "epiphyseal stippling of the first metacarpal": [ + "HP:0010024" + ], + "speckled calcification in the end part of the first long bone of hand": [ + "HP:0010024" + ], + "speckled calcifications in the end part of the first long bone of hand": [ + "HP:0010024" + ], + "stippling of the epiphysis of the 1st metacarpal": [ + "HP:0010024" + ], + "triangular epiphysis of the 1st metacarpal": [ + "HP:0010025" + ], + "triangular end part of the 1st long bone of hand": [ + "HP:0010025" + ], + "aplasia / hypoplasia of the 1st metacarpal": [ + "HP:0010026" + ], + "absent / small 1st long bone of hand": [ + "HP:0010026" + ], + "absent / underdevelop 1st long bone of hand": [ + "HP:0010026" + ], + "absent / underdeveloped 1st long bone of hand": [ + "HP:0010026" + ], + "broad 1st metacarpal": [ + "HP:0010027" + ], + "wide 1st long bone of hand": [ + "HP:0010027" + ], + "bullet - shape 1st metacarpal": [ + "HP:0010028" + ], + "bullet - shaped 1st metacarpal": [ + "HP:0010028" + ], + "bullet - shape 1st long bone of hand": [ + "HP:0010028" + ], + "bullet - shaped 1st long bone of hand": [ + "HP:0010028" + ], + "curve 1st metacarpal": [ + "HP:0010029" + ], + "curved 1st metacarpal": [ + "HP:0010029" + ], + "curve 1st long bone of hand": [ + "HP:0010029" + ], + "curved 1st long bone of hand": [ + "HP:0010029" + ], + "osteolytic defect of the 1st metacarpal": [ + "HP:0010030" + ], + "osteolytic defects of the 1st metacarpal": [ + "HP:0010030" + ], + "patchy sclerosis of the 1st metacarpal": [ + "HP:0010031" + ], + "uneven increase in bone density in 1st long bone of hand": [ + "HP:0010031" + ], + "triangular shape 1st metacarpal": [ + "HP:0010033" + ], + "triangular shaped 1st metacarpal": [ + "HP:0010033" + ], + "triangular shape 1st long bone of hand": [ + "HP:0010033" + ], + "triangular shaped 1st long bone of hand": [ + "HP:0010033" + ], + "short 1st metacarpal": [ + "HP:0010034" + ], + "first metacarpal hypoplasia": [ + "HP:0010034" + ], + "first metacarpal hypoplastic": [ + "HP:0010034" + ], + "first metacarpals hypoplastic": [ + "HP:0010034" + ], + "hypoplastic 1st metacarpal": [ + "HP:0010034" + ], + "short first metacarpal": [ + "HP:0010034" + ], + "short first metacarpals": [ + "HP:0010034" + ], + "shorten 1st long bone of hand": [ + "HP:0010034" + ], + "shortened 1st long bone of hand": [ + "HP:0010034" + ], + "aplasia of the 1st metacarpal": [ + "HP:0010035" + ], + "absent 1st long bone of hand": [ + "HP:0010035" + ], + "absent first metacarpal": [ + "HP:0010035" + ], + "aplasia / hypoplasia of the 2nd metacarpal": [ + "HP:0010036" + ], + "absent / small 2nd long bone of hand": [ + "HP:0010036" + ], + "absent / underdevelop 2nd long bone of hand": [ + "HP:0010036" + ], + "absent / underdeveloped 2nd long bone of hand": [ + "HP:0010036" + ], + "aplasia of the 2nd metacarpal": [ + "HP:0010037" + ], + "absent 2nd long bone of hand": [ + "HP:0010037" + ], + "short 2nd metacarpal": [ + "HP:0010038" + ], + "hypoplastic 2nd metacarpal": [ + "HP:0010038" + ], + "rudimentary 2nd metacarpal": [ + "HP:0010038" + ], + "shorten 2nd long bone of hand": [ + "HP:0010038" + ], + "shortened 2nd long bone of hand": [ + "HP:0010038" + ], + "aplasia / hypoplasia of the 3rd metacarpal": [ + "HP:0010039" + ], + "absent / small 3rd long bone of hand": [ + "HP:0010039" + ], + "absent / underdevelop 3rd long bone of hand": [ + "HP:0010039" + ], + "absent / underdeveloped 3rd long bone of hand": [ + "HP:0010039" + ], + "aplasia of the 3rd metacarpal": [ + "HP:0010040" + ], + "absent 3rd long bone of hand": [ + "HP:0010040" + ], + "short 3rd metacarpal": [ + "HP:0010041" + ], + "hypoplastic 3rd metacarpal": [ + "HP:0010041" + ], + "short third metacarpal": [ + "HP:0010041" + ], + "short third metacarpals": [ + "HP:0010041" + ], + "shorten 3rd long bone of hand": [ + "HP:0010041" + ], + "shortened 3rd long bone of hand": [ + "HP:0010041" + ], + "small 3rd metacarpal": [ + "HP:0010041" + ], + "small 3rd metacarpals": [ + "HP:0010041" + ], + "aplasia / hypoplasia of the 4th metacarpal": [ + "HP:0010042" + ], + "absent / small 4th long bone of hand": [ + "HP:0010042" + ], + "absent / underdevelop 4th long bone of hand": [ + "HP:0010042" + ], + "absent / underdeveloped 4th long bone of hand": [ + "HP:0010042" + ], + "aplasia of the 4th metacarpal": [ + "HP:0010043" + ], + "absent 4th long bone of hand": [ + "HP:0010043" + ], + "short 4th metacarpal": [ + "HP:0010044" + ], + "hypoplastic fourth metacarpal": [ + "HP:0010044" + ], + "short 4th metacarpals": [ + "HP:0010044" + ], + "short fourth metacarpal": [ + "HP:0010044" + ], + "short fourth metacarpals": [ + "HP:0010044" + ], + "shorten 4th long bone of hand": [ + "HP:0010044" + ], + "shortened 4th long bone of hand": [ + "HP:0010044" + ], + "aplasia / hypoplasia of the 5th metacarpal": [ + "HP:0010045" + ], + "absent / small 5th long bone of hand": [ + "HP:0010045" + ], + "absent / underdevelop 5th long bone of hand": [ + "HP:0010045" + ], + "absent / underdeveloped 5th long bone of hand": [ + "HP:0010045" + ], + "aplasia of the 5th metacarpal": [ + "HP:0010046" + ], + "absent 5th long bone of hand": [ + "HP:0010046" + ], + "absent 5th metacarpal": [ + "HP:0010046" + ], + "short 5th metacarpal": [ + "HP:0010047" + ], + "fifth metacarpal hypoplasia": [ + "HP:0010047" + ], + "hypoplastic 5th metacarpal": [ + "HP:0010047" + ], + "short fifth metacarpal": [ + "HP:0010047" + ], + "short fifth metacarpals": [ + "HP:0010047" + ], + "shorten 5th long bone of hand": [ + "HP:0010047" + ], + "shortened 5th long bone of hand": [ + "HP:0010047" + ], + "aplasia of metacarpal bone": [ + "HP:0010048" + ], + "aplasia of metacarpal bones": [ + "HP:0010048" + ], + "absent long bone of hand": [ + "HP:0010048" + ], + "absent metacarpal": [ + "HP:0010048" + ], + "absent metacarpals": [ + "HP:0010048" + ], + "short metacarpal": [ + "HP:0010049" + ], + "brachymetacarpalia": [ + "HP:0010049" + ], + "metacarpal hypoplasia": [ + "HP:0010049" + ], + "short metacarpal bone": [ + "HP:0010049" + ], + "short metacarpal bones": [ + "HP:0010049" + ], + "short metacarpals": [ + "HP:0010049" + ], + "shorten long bone of hand": [ + "HP:0010049" + ], + "shortened long bone of hand": [ + "HP:0010049" + ], + "shortened long bones of hand": [ + "HP:0010049" + ], + "shorten metacarpal": [ + "HP:0010049" + ], + "shortened metacarpals": [ + "HP:0010049" + ], + "shortening of metacarpal": [ + "HP:0010049" + ], + "shortening of metacarpals": [ + "HP:0010049" + ], + "deviation of the hallux": [ + "HP:0010051" + ], + "displacement of big toe": [ + "HP:0010051" + ], + "displacement of the hallux": [ + "HP:0010051" + ], + "abnormal morphology of the proximal phalanx of the hallux": [ + "HP:0010052" + ], + "abnormal innermost big toe bone": [ + "HP:0010052" + ], + "abnormality of the proximal phalanx of the hallux": [ + "HP:0010052" + ], + "abnormality of the distal phalanx of the hallux": [ + "HP:0010053" + ], + "abnormality of the outermost bone of the big toe": [ + "HP:0010053" + ], + "abnormality of the first metatarsal bone": [ + "HP:0010054" + ], + "abnormality of the 1st long bone of foot": [ + "HP:0010054" + ], + "broad hallux": [ + "HP:0010055" + ], + "abnormally broad great toe": [ + "HP:0010055" + ], + "abnormally broad great toes": [ + "HP:0010055" + ], + "broad big toe": [ + "HP:0010055" + ], + "broad great toe": [ + "HP:0010055" + ], + "broad great toes": [ + "HP:0010055" + ], + "broad halluces": [ + "HP:0010055" + ], + "wide big toe": [ + "HP:0010055" + ], + "abnormality of the epiphysis of the hallux": [ + "HP:0010056" + ], + "abnormality of the epiphyses of the hallux": [ + "HP:0010056" + ], + "abnormality of the end part of the big toe bone": [ + "HP:0010056" + ], + "abnormality of the phalanx of the hallux": [ + "HP:0010057" + ], + "abnormality of the phalanges of the hallux": [ + "HP:0010057" + ], + "abnormal big toe bone": [ + "HP:0010057" + ], + "abnormal big toe bones": [ + "HP:0010057" + ], + "aplasia / hypoplasia of the phalanx of the hallux": [ + "HP:0010058" + ], + "aplasia / hypoplasia of the phalanges of the hallux": [ + "HP:0010058" + ], + "absent / small big toe bone": [ + "HP:0010058" + ], + "absent / underdevelop big toe bone": [ + "HP:0010058" + ], + "absent / underdeveloped big toe bone": [ + "HP:0010058" + ], + "broad hallux phalanx": [ + "HP:0010059" + ], + "broad bone of big toe": [ + "HP:0010059" + ], + "broad phalanx of the hallux": [ + "HP:0010059" + ], + "broad phalanges of the hallux": [ + "HP:0010059" + ], + "wide bone of big toe": [ + "HP:0010059" + ], + "bullet - shape hallux phalanx": [ + "HP:0010060" + ], + "bullet - shaped hallux phalanx": [ + "HP:0010060" + ], + "bullet - shape bone of big toe": [ + "HP:0010060" + ], + "bullet - shaped bone of big toe": [ + "HP:0010060" + ], + "bullet - shaped phalanx of the hallux": [ + "HP:0010060" + ], + "bullet - shaped phalanges of the hallux": [ + "HP:0010060" + ], + "curve hallux phalanx": [ + "HP:0010061" + ], + "curved hallux phalanx": [ + "HP:0010061" + ], + "curve bone of big toe": [ + "HP:0010061" + ], + "curve bones of big toe": [ + "HP:0010061" + ], + "curve phalanx of the hallux": [ + "HP:0010061" + ], + "curved phalanges of the hallux": [ + "HP:0010061" + ], + "osteolytic defect of the phalanx of the hallux": [ + "HP:0010062" + ], + "osteolytic defects of the phalanges of the hallux": [ + "HP:0010062" + ], + "patchy sclerosis of hallux phalanx": [ + "HP:0010063" + ], + "patchy sclerosis of the phalanx of the hallux": [ + "HP:0010063" + ], + "patchy sclerosis of the phalanges of the hallux": [ + "HP:0010063" + ], + "uneven increase in bone density in big toe bone": [ + "HP:0010063" + ], + "symphalangism affect the phalanx of the hallux": [ + "HP:0010064" + ], + "symphalangism affecting the phalanges of the hallux": [ + "HP:0010064" + ], + "fuse big toe bone": [ + "HP:0010064" + ], + "fused big toe bones": [ + "HP:0010064" + ], + "hallucal symphalangism": [ + "HP:0010064" + ], + "triangular shape phalanx of the hallux": [ + "HP:0010065" + ], + "triangular shaped phalanges of the hallux": [ + "HP:0010065" + ], + "triangular shape bone of big toe": [ + "HP:0010065" + ], + "triangular shaped bones of big toe": [ + "HP:0010065" + ], + "duplication of phalanx of hallux": [ + "HP:0010066" + ], + "duplicate hallux": [ + "HP:0010066" + ], + "duplicated hallux": [ + "HP:0010066" + ], + "duplication of big toe bone": [ + "HP:0010066" + ], + "duplication of great toe": [ + "HP:0010066" + ], + "duplication of great toes": [ + "HP:0010066" + ], + "duplication of phalanx of big toe": [ + "HP:0010066" + ], + "hallucal duplication": [ + "HP:0010066" + ], + "partial / complete duplication of the phalanx of the hallux": [ + "HP:0010066" + ], + "partial / complete duplication of the phalanges of the hallux": [ + "HP:0010066" + ], + "aplasia / hypoplasia of the 1st metatarsal": [ + "HP:0010067" + ], + "absent / small 1st long bone of foot": [ + "HP:0010067" + ], + "absent / underdevelop 1st long bone of foot": [ + "HP:0010067" + ], + "absent / underdeveloped 1st long bone of foot": [ + "HP:0010067" + ], + "broad first metatarsal": [ + "HP:0010068" + ], + "broad 1st metatarsal": [ + "HP:0010068" + ], + "enlarge first metatarsal": [ + "HP:0010068" + ], + "enlarged first metatarsal": [ + "HP:0010068" + ], + "wide 1st long bone of foot": [ + "HP:0010068" + ], + "bullet - shape 1st metatarsal": [ + "HP:0010069" + ], + "bullet - shaped 1st metatarsal": [ + "HP:0010069" + ], + "bullet - shape 1st long bone of foot": [ + "HP:0010069" + ], + "bullet - shaped 1st long bone of foot": [ + "HP:0010069" + ], + "curve 1st metatarsal": [ + "HP:0010070" + ], + "curved 1st metatarsal": [ + "HP:0010070" + ], + "curve 1st long bone of foot": [ + "HP:0010070" + ], + "curved 1st long bone of foot": [ + "HP:0010070" + ], + "osteolytic defect of the 1st metatarsal": [ + "HP:0010071" + ], + "osteolytic defects of the 1st metatarsal": [ + "HP:0010071" + ], + "patchy sclerosis of the 1st metatarsal": [ + "HP:0010072" + ], + "uneven increase in bone density of the 1st long bone of foot": [ + "HP:0010072" + ], + "synostosis involve the 1st metatarsal": [ + "HP:0010073" + ], + "synostosis involving the 1st metatarsal": [ + "HP:0010073" + ], + "fusion involve the 1st long bone of foot": [ + "HP:0010073" + ], + "fusion involving the 1st long bone of foot": [ + "HP:0010073" + ], + "triangular shape 1st metatarsal": [ + "HP:0010074" + ], + "triangular shaped 1st metatarsal": [ + "HP:0010074" + ], + "triangular shape 1st long bone of foot": [ + "HP:0010074" + ], + "triangular shaped 1st long bone of foot": [ + "HP:0010074" + ], + "duplication of the 1st metatarsal": [ + "HP:0010075" + ], + "duplicate 1st long bone of foot": [ + "HP:0010075" + ], + "duplicated 1st long bone of foot": [ + "HP:0010075" + ], + "duplicate first metatarsal": [ + "HP:0010075" + ], + "duplicated first metatarsals": [ + "HP:0010075" + ], + "aplasia / hypoplasia of the distal phalanx of the hallux": [ + "HP:0010076" + ], + "absent / small outermost big toe bone": [ + "HP:0010076" + ], + "absent / underdevelop outermost big toe bone": [ + "HP:0010076" + ], + "absent / underdeveloped outermost big toe bone": [ + "HP:0010076" + ], + "broad distal phalanx of the hallux": [ + "HP:0010077" + ], + "broad outermost bone of big toe": [ + "HP:0010077" + ], + "wide outermost bone of big toe": [ + "HP:0010077" + ], + "bullet - shaped distal phalanx of the hallux": [ + "HP:0010078" + ], + "bullet - shape outermost bone of big toe": [ + "HP:0010078" + ], + "bullet - shaped outermost bone of big toe": [ + "HP:0010078" + ], + "curve distal phalanx of the hallux": [ + "HP:0010079" + ], + "curved distal phalanx of the hallux": [ + "HP:0010079" + ], + "curve outermost bone of big toe": [ + "HP:0010079" + ], + "curved outermost bone of big toe": [ + "HP:0010079" + ], + "osteolytic defect of the distal phalanx of the hallux": [ + "HP:0010080" + ], + "osteolytic defects of the distal phalanx of the hallux": [ + "HP:0010080" + ], + "patchy sclerosis of the distal phalanx of the hallux": [ + "HP:0010081" + ], + "uneven increase in bone density in the outermost bone of big toe": [ + "HP:0010081" + ], + "symphalangism affect the distal phalanx of the hallux": [ + "HP:0010082" + ], + "symphalangism affecting the distal phalanx of the hallux": [ + "HP:0010082" + ], + "fuse outermost bone of big toe": [ + "HP:0010082" + ], + "fused outermost bone of big toe": [ + "HP:0010082" + ], + "triangular shape distal phalanx of the hallux": [ + "HP:0010083" + ], + "triangular shaped distal phalanx of the hallux": [ + "HP:0010083" + ], + "triangular shape outermost bone of the big toe": [ + "HP:0010083" + ], + "triangular shaped outermost bone of the big toe": [ + "HP:0010083" + ], + "duplication of the distal phalanx of the hallux": [ + "HP:0010084" + ], + "duplication of the outermost bone of big toe": [ + "HP:0010084" + ], + "partial / complete duplication of the distal phalanx of the hallux": [ + "HP:0010084" + ], + "aplasia / hypoplasia of the proximal phalanx of the hallux": [ + "HP:0010085" + ], + "absent / small innermost big toe bone": [ + "HP:0010085" + ], + "absent / underdevelop innermost big toe bone": [ + "HP:0010085" + ], + "absent / underdeveloped innermost big toe bone": [ + "HP:0010085" + ], + "broad proximal phalanx of the hallux": [ + "HP:0010086" + ], + "broad innermost bone of the big toe": [ + "HP:0010086" + ], + "broad proximal phalanx of the big toe": [ + "HP:0010086" + ], + "bullet - shape proximal phalanx of the hallux": [ + "HP:0010087" + ], + "bullet - shaped proximal phalanx of the hallux": [ + "HP:0010087" + ], + "bullet - shape innermost bone of the big toe": [ + "HP:0010087" + ], + "bullet - shaped innermost bone of the big toe": [ + "HP:0010087" + ], + "curve proximal phalanx of the hallux": [ + "HP:0010088" + ], + "curved proximal phalanx of the hallux": [ + "HP:0010088" + ], + "curve innermost bone of the big toe": [ + "HP:0010088" + ], + "curved innermost bone of the big toe": [ + "HP:0010088" + ], + "osteolytic defect of the proximal phalanx of the hallux": [ + "HP:0010089" + ], + "osteolytic defects of the proximal phalanx of the hallux": [ + "HP:0010089" + ], + "patchy sclerosis of the proximal phalanx of the hallux": [ + "HP:0010090" + ], + "uneven increase in bone density in the innermost bone of the big toe": [ + "HP:0010090" + ], + "symphalangism affect the proximal phalanx of the hallux": [ + "HP:0010091" + ], + "symphalangism affecting the proximal phalanx of the hallux": [ + "HP:0010091" + ], + "fuse innermost bone of big toe": [ + "HP:0010091" + ], + "fused innermost bone of big toe": [ + "HP:0010091" + ], + "triangular shape proximal phalanx of the hallux": [ + "HP:0010092" + ], + "triangular shaped proximal phalanx of the hallux": [ + "HP:0010092" + ], + "triangular shape innermost bone of big toe": [ + "HP:0010092" + ], + "triangular shaped innermost bone of big toe": [ + "HP:0010092" + ], + "duplication of the proximal phalanx of the hallux": [ + "HP:0010093" + ], + "duplication of the innermost bone of big toe": [ + "HP:0010093" + ], + "complete duplication of the proximal phalanx of the hallux": [ + "HP:0010094" + ], + "complete duplication of the innermost bone of big toe": [ + "HP:0010094" + ], + "partial duplication of the proximal phalanx of the hallux": [ + "HP:0010095" + ], + "partial duplication of the innermost bone of big toe": [ + "HP:0010095" + ], + "complete duplication of the distal phalanx of the hallux": [ + "HP:0010096" + ], + "complete duplication of the outermost bone of the big toe": [ + "HP:0010096" + ], + "partial duplication of the distal phalanx of the hallux": [ + "HP:0010097" + ], + "bifid distal phalanx of hallux": [ + "HP:0010097" + ], + "notch outermost bone of big toe": [ + "HP:0010097" + ], + "notched outermost bone of big toe": [ + "HP:0010097" + ], + "partial duplication of the outermost bone of big toe": [ + "HP:0010097" + ], + "complete duplication of the 1st metatarsal": [ + "HP:0010098" + ], + "complete duplication of the 1st long bone of foot": [ + "HP:0010098" + ], + "partial duplication of the 1st metatarsal": [ + "HP:0010099" + ], + "partial duplication of the 1st long bone of foot": [ + "HP:0010099" + ], + "complete duplication of hallux phalanx": [ + "HP:0010100" + ], + "complete duplication of big toe bone": [ + "HP:0010100" + ], + "complete duplication of big toe bones": [ + "HP:0010100" + ], + "complete duplication of the phalanx of the hallux": [ + "HP:0010100" + ], + "complete duplication of the phalanges of the hallux": [ + "HP:0010100" + ], + "partial duplication of the phalanx of the hallux": [ + "HP:0010101" + ], + "partial duplication of the phalanges of the hallux": [ + "HP:0010101" + ], + "partial duplication of big toe": [ + "HP:0010101" + ], + "partial duplication of hallux": [ + "HP:0010101" + ], + "aplasia of the distal phalanx of the hallux": [ + "HP:0010102" + ], + "absent outermost bone of big toe": [ + "HP:0010102" + ], + "short distal phalanx of hallux": [ + "HP:0010103" + ], + "hypoplastic / small distal phalanx of the hallux": [ + "HP:0010103" + ], + "small distal phalanx of big toe": [ + "HP:0010103" + ], + "small distal phalanx of hallux": [ + "HP:0010103" + ], + "small outermost bone of big toe": [ + "HP:0010103" + ], + "absent first metatarsal": [ + "HP:0010104" + ], + "absent 1st long bone of foot": [ + "HP:0010104" + ], + "absent 1st metatarsal": [ + "HP:0010104" + ], + "aplasia of the 1st metatarsal": [ + "HP:0010104" + ], + "short first metatarsal": [ + "HP:0010105" + ], + "first metatarsal hypoplasia": [ + "HP:0010105" + ], + "first metatarsal hypoplastic": [ + "HP:0010105" + ], + "first metatarsals hypoplastic": [ + "HP:0010105" + ], + "short 1st long bone of foot": [ + "HP:0010105" + ], + "aplasia of the proximal phalanx of the hallux": [ + "HP:0010106" + ], + "absent innermost bone of big toe": [ + "HP:0010106" + ], + "short proximal phalanx of hallux": [ + "HP:0010107" + ], + "hypoplastic proximal phalanx of the hallux": [ + "HP:0010107" + ], + "short innermost big toe bone": [ + "HP:0010107" + ], + "short proximal phalanges of halluces": [ + "HP:0010107" + ], + "short proximal phalanx of halluces": [ + "HP:0010107" + ], + "small proximal phalanx of big toe": [ + "HP:0010107" + ], + "small proximal phalanx of hallux": [ + "HP:0010107" + ], + "short hallux": [ + "HP:0010109" + ], + "hypoplastic big toe": [ + "HP:0010109" + ], + "hypoplastic big toes": [ + "HP:0010109" + ], + "hypoplastic hallux": [ + "HP:0010109" + ], + "short big toe": [ + "HP:0010109" + ], + "short halluces": [ + "HP:0010109" + ], + "small hallux": [ + "HP:0010109" + ], + "aplasia of the phalanx of the hallux": [ + "HP:0010110" + ], + "aplasia of the phalanges of the hallux": [ + "HP:0010110" + ], + "absent bone of big toe": [ + "HP:0010110" + ], + "short phalanx of hallux": [ + "HP:0010111" + ], + "hypoplastic phalanx of the hallux": [ + "HP:0010111" + ], + "hypoplastic phalanges of the hallux": [ + "HP:0010111" + ], + "short bone of big toe": [ + "HP:0010111" + ], + "mesoaxial foot polydactyly": [ + "HP:0010112" + ], + "central polydactyly of foot": [ + "HP:0010112" + ], + "central polydactyly of feet": [ + "HP:0010112" + ], + "absent hallux epiphysis": [ + "HP:0010113" + ], + "absent end part of big toe bone": [ + "HP:0010113" + ], + "absent epiphysis of the hallux": [ + "HP:0010113" + ], + "absent epiphyses of the hallux": [ + "HP:0010113" + ], + "bracket epiphysis of the hallux": [ + "HP:0010114" + ], + "bracket epiphyses of the hallux": [ + "HP:0010114" + ], + "bracket shape end part of big toe bone": [ + "HP:0010114" + ], + "bracket shaped end part of big toe bone": [ + "HP:0010114" + ], + "cone - shaped epiphysis of the hallux": [ + "HP:0010115" + ], + "cone - shaped epiphyses of the hallux": [ + "HP:0010115" + ], + "cone - shaped end part of the big toe bone": [ + "HP:0010115" + ], + "enlarged epiphysis of the hallux": [ + "HP:0010116" + ], + "enlarged epiphyses of the hallux": [ + "HP:0010116" + ], + "enlarged end part of the big toe bone": [ + "HP:0010116" + ], + "fragmentation of the epiphysis of the hallux": [ + "HP:0010117" + ], + "fragmentation of the epiphyses of the hallux": [ + "HP:0010117" + ], + "fragmentation of the end part of the big toe bone": [ + "HP:0010117" + ], + "irregular epiphysis of the hallux": [ + "HP:0010118" + ], + "irregular epiphyses of the hallux": [ + "HP:0010118" + ], + "irregular end part of big toe bone": [ + "HP:0010118" + ], + "ivory epiphysis of the hallux": [ + "HP:0010119" + ], + "ivory epiphyses of the hallux": [ + "HP:0010119" + ], + "increase bone density of end part of the big toe bone": [ + "HP:0010119" + ], + "increased bone density of end part of the big toe bone": [ + "HP:0010119" + ], + "pseudoepiphyses of the hallux": [ + "HP:0010120" + ], + "small epiphysis of the hallux": [ + "HP:0010121" + ], + "small epiphyses of the hallux": [ + "HP:0010121" + ], + "small end part of the big toe bone": [ + "HP:0010121" + ], + "stippling of the epiphysis of the hallux": [ + "HP:0010122" + ], + "stippling of the epiphyses of the hallux": [ + "HP:0010122" + ], + "speckled calcification in the end part of the big toe bone": [ + "HP:0010122" + ], + "speckled calcifications in the end part of the big toe bone": [ + "HP:0010122" + ], + "triangular epiphysis of the hallux": [ + "HP:0010123" + ], + "triangular epiphyses of the hallux": [ + "HP:0010123" + ], + "triangular end part of the big toe bone": [ + "HP:0010123" + ], + "abnormality of the epiphysis of the distal phalanx of the hallux": [ + "HP:0010124" + ], + "abnormality of the end part of the outermost bone of the big toe bone": [ + "HP:0010124" + ], + "abnormality of the epiphysis of the 1st metatarsal": [ + "HP:0010125" + ], + "abnormality of the end part of the 1st long bone of foot": [ + "HP:0010125" + ], + "abnormality of the epiphysis of the proximal phalanx of the hallux": [ + "HP:0010126" + ], + "abnormality of the end part of the innermost bone of the big toe": [ + "HP:0010126" + ], + "absent epiphysis of the proximal phalanx of the hallux": [ + "HP:0010127" + ], + "absent end part of the innermost bone of the big toe": [ + "HP:0010127" + ], + "bracket epiphysis of the proximal phalanx of the hallux": [ + "HP:0010128" + ], + "bracket shape end part of the innermost bone of big toe": [ + "HP:0010128" + ], + "bracket shaped end part of the innermost bone of big toe": [ + "HP:0010128" + ], + "cone - shaped epiphysis of the proximal phalanx of the hallux": [ + "HP:0010129" + ], + "cone - shaped end part of the innermost bone of the big toe": [ + "HP:0010129" + ], + "enlarged epiphysis of the proximal phalanx of the hallux": [ + "HP:0010130" + ], + "enlarged end part of the innermost bone of the big toe": [ + "HP:0010130" + ], + "fragmentation of the epiphysis of the proximal phalanx of the hallux": [ + "HP:0010131" + ], + "fragmentation of the end part of the innermost bone of the big toe": [ + "HP:0010131" + ], + "irregular epiphysis of the proximal phalanx of the hallux": [ + "HP:0010132" + ], + "irregular end part of the innermost bone of the big toe": [ + "HP:0010132" + ], + "ivory epiphysis of the proximal phalanx of the hallux": [ + "HP:0010133" + ], + "increase bone density of end part of the innermost bone of the big toe": [ + "HP:0010133" + ], + "increased bone density of end part of the innermost bone of the big toe": [ + "HP:0010133" + ], + "pseudoepiphysis of the proximal phalanx of the hallux": [ + "HP:0010134" + ], + "small epiphysis of the proximal phalanx of the hallux": [ + "HP:0010135" + ], + "small end part of the innermost bone of the big toe": [ + "HP:0010135" + ], + "stippling of the epiphysis of the proximal phalanx of the hallux": [ + "HP:0010136" + ], + "speckled calcification in the end part of the innermost bone of the big toe": [ + "HP:0010136" + ], + "speckled calcifications in the end part of the innermost bone of the big toe": [ + "HP:0010136" + ], + "triangular epiphysis of the proximal phalanx of the hallux": [ + "HP:0010137" + ], + "triangular end part of the innermost bone of the big toe": [ + "HP:0010137" + ], + "absent epiphysis of the distal phalanx of the hallux": [ + "HP:0010138" + ], + "absent end part of the outermost bone of the big toe": [ + "HP:0010138" + ], + "bracket epiphysis of the distal phalanx of the hallux": [ + "HP:0010139" + ], + "bracket shape end part of the outermost bone of big toe": [ + "HP:0010139" + ], + "bracket shaped end part of the outermost bone of big toe": [ + "HP:0010139" + ], + "cone - shaped epiphysis of the distal phalanx of the hallux": [ + "HP:0010140" + ], + "cone - shaped end part of the outermost bone of the big toe": [ + "HP:0010140" + ], + "enlarged epiphysis of the distal phalanx of the hallux": [ + "HP:0010141" + ], + "enlarged end part of the outermost bone of the big toe": [ + "HP:0010141" + ], + "fragmentation of the epiphysis of the distal phalanx of the hallux": [ + "HP:0010142" + ], + "fragmentation of the end part of the outermost bone of the big toe": [ + "HP:0010142" + ], + "irregular epiphysis of the distal phalanx of the hallux": [ + "HP:0010143" + ], + "irregular end part of the outermost bone of the big toe": [ + "HP:0010143" + ], + "ivory epiphysis of the distal phalanx of the hallux": [ + "HP:0010144" + ], + "increase bone density of end part of the outermost bone of the big toe": [ + "HP:0010144" + ], + "increased bone density of end part of the outermost bone of the big toe": [ + "HP:0010144" + ], + "pseudoepiphysis of the distal phalanx of the hallux": [ + "HP:0010145" + ], + "small epiphysis of the distal phalanx of the hallux": [ + "HP:0010146" + ], + "small end part of the outermost bone of the big toe": [ + "HP:0010146" + ], + "stippling of the epiphysis of the distal phalanx of the hallux": [ + "HP:0010147" + ], + "speckled calcification in the end part of the outermost bone of the big toe": [ + "HP:0010147" + ], + "speckled calcifications in the end part of the outermost bone of the big toe": [ + "HP:0010147" + ], + "triangular epiphysis of the distal phalanx of the hallux": [ + "HP:0010148" + ], + "triangular end part of the outermost bone of the big toe": [ + "HP:0010148" + ], + "absent epiphysis of the 1st metatarsal": [ + "HP:0010149" + ], + "absent end part of the 1st long bone of foot": [ + "HP:0010149" + ], + "bracket epiphysis of the 1st metatarsal": [ + "HP:0010150" + ], + "bracket shape end part of 1st long bone of foot": [ + "HP:0010150" + ], + "bracket shaped end part of 1st long bone of foot": [ + "HP:0010150" + ], + "cone - shaped epiphysis of the 1st metatarsal": [ + "HP:0010151" + ], + "cone - shaped end part of the 1st long bone of foot": [ + "HP:0010151" + ], + "enlarged epiphysis of the 1st metatarsal": [ + "HP:0010152" + ], + "enlarged end part of the 1st long bone of foot": [ + "HP:0010152" + ], + "fragmentation of the epiphysis of the 1st metatarsal": [ + "HP:0010153" + ], + "fragmentation of the end part of the 1st long bone of foot": [ + "HP:0010153" + ], + "irregular epiphysis of the 1st metatarsal": [ + "HP:0010154" + ], + "irregular end part of the 1st long bone of foot": [ + "HP:0010154" + ], + "ivory epiphysis of the 1st metatarsal": [ + "HP:0010155" + ], + "increase bone density of end part of the 1st long bone of foot": [ + "HP:0010155" + ], + "increased bone density of end part of the 1st long bone of foot": [ + "HP:0010155" + ], + "pseudoepiphysis of the 1st metatarsal": [ + "HP:0010156" + ], + "small epiphysis of the 1st metatarsal": [ + "HP:0010157" + ], + "small end part of the 1st long bone of foot": [ + "HP:0010157" + ], + "stippling of the epiphysis of the 1st metatarsal": [ + "HP:0010158" + ], + "speckled calcification in the end part of the 1st long bone of foot": [ + "HP:0010158" + ], + "speckled calcifications in the end part of the 1st long bone of foot": [ + "HP:0010158" + ], + "triangular epiphysis of the 1st metatarsal": [ + "HP:0010159" + ], + "triangular end part of the 1st long bone of foot": [ + "HP:0010159" + ], + "abnormality of the epiphysis of the toe": [ + "HP:0010160" + ], + "abnormality of the epiphyses of the toes": [ + "HP:0010160" + ], + "abnormality of the end part of the toe bone": [ + "HP:0010160" + ], + "abnormality of the end part of the toe bones": [ + "HP:0010160" + ], + "abnormality of the phalanx of the toe": [ + "HP:0010161" + ], + "abnormality of the phalanges of the toes": [ + "HP:0010161" + ], + "abnormality of the long bone of the toe": [ + "HP:0010161" + ], + "abnormality of the long bones of the toes": [ + "HP:0010161" + ], + "absent epiphysis of the toe": [ + "HP:0010162" + ], + "absent epiphyses of the toes": [ + "HP:0010162" + ], + "absent end part of the toe bone": [ + "HP:0010162" + ], + "absent end part of the toe bones": [ + "HP:0010162" + ], + "bracket epiphysis of the toe": [ + "HP:0010163" + ], + "bracket epiphyses of the toes": [ + "HP:0010163" + ], + "bracket shape end part of the toe bone": [ + "HP:0010163" + ], + "bracket shaped end part of the toe bones": [ + "HP:0010163" + ], + "cone - shaped epiphysis of the toe": [ + "HP:0010164" + ], + "cone - shaped epiphyses of the toes": [ + "HP:0010164" + ], + "cone - shaped end part of the toe bone": [ + "HP:0010164" + ], + "cone - shaped end part of the toe bones": [ + "HP:0010164" + ], + "enlarged epiphysis of the toe": [ + "HP:0010165" + ], + "enlarged epiphyses of the toes": [ + "HP:0010165" + ], + "enlarged end part of the toe bone": [ + "HP:0010165" + ], + "enlarged end part of the toe bones": [ + "HP:0010165" + ], + "fragmentation of the epiphysis of the toe": [ + "HP:0010166" + ], + "fragmentation of the epiphyses of the toes": [ + "HP:0010166" + ], + "fragmentation of the end part of the toe bone": [ + "HP:0010166" + ], + "fragmentation of the end part of the toe bones": [ + "HP:0010166" + ], + "irregular epiphysis of the toe": [ + "HP:0010167" + ], + "irregular epiphyses of the toes": [ + "HP:0010167" + ], + "irregular end part of the toe bone": [ + "HP:0010167" + ], + "irregular end part of the toe bones": [ + "HP:0010167" + ], + "ivory epiphysis of the toe": [ + "HP:0010168" + ], + "ivory epiphyses of the toes": [ + "HP:0010168" + ], + "increase bone density of end part of the toe": [ + "HP:0010168" + ], + "increased bone density of end part of the toes": [ + "HP:0010168" + ], + "pseudoepiphyses of the toe": [ + "HP:0010169" + ], + "pseudoepiphyses of the toes": [ + "HP:0010169" + ], + "small epiphysis of the toe": [ + "HP:0010170" + ], + "small epiphyses of the toes": [ + "HP:0010170" + ], + "small end part of the toe bone": [ + "HP:0010170" + ], + "small end part of the toe bones": [ + "HP:0010170" + ], + "epiphyseal stippling of toe phalanx": [ + "HP:0010171" + ], + "epiphyseal stippling of toe phalanges": [ + "HP:0010171" + ], + "speckled calcification in long toe bone": [ + "HP:0010171" + ], + "speckled calcifications in long toe bones": [ + "HP:0010171" + ], + "stippling of the epiphysis of the toe": [ + "HP:0010171" + ], + "stippling of the epiphyses of the toes": [ + "HP:0010171" + ], + "triangular epiphysis of the toe": [ + "HP:0010172" + ], + "triangular epiphyses of the toes": [ + "HP:0010172" + ], + "triangular end part of the toe bone": [ + "HP:0010172" + ], + "triangular end part of the toe bones": [ + "HP:0010172" + ], + "aplasia / hypoplasia of the phalanx of the toe": [ + "HP:0010173" + ], + "aplasia / hypoplasia of the phalanges of the toes": [ + "HP:0010173" + ], + "absent / small toe bone": [ + "HP:0010173" + ], + "absent / small toe bones": [ + "HP:0010173" + ], + "absent / underdevelop toe bone": [ + "HP:0010173" + ], + "absent / underdeveloped toe bones": [ + "HP:0010173" + ], + "broad phalanx of the toe": [ + "HP:0010174" + ], + "broad phalanx of the toes": [ + "HP:0010174" + ], + "wide toe bone": [ + "HP:0010174" + ], + "wide toe bones": [ + "HP:0010174" + ], + "bullet - shape toe phalanx": [ + "HP:0010175" + ], + "bullet - shaped toe phalanx": [ + "HP:0010175" + ], + "bullet - shaped phalanx of the toe": [ + "HP:0010175" + ], + "bullet - shaped phalanges of the toes": [ + "HP:0010175" + ], + "bullet - shape toe bone": [ + "HP:0010175" + ], + "bullet - shaped toe bone": [ + "HP:0010175" + ], + "curve toe phalanx": [ + "HP:0010176" + ], + "curved toe phalanx": [ + "HP:0010176" + ], + "curve phalanx of the toe": [ + "HP:0010176" + ], + "curved phalanges of the toes": [ + "HP:0010176" + ], + "curve toe bone": [ + "HP:0010176" + ], + "curved toe bone": [ + "HP:0010176" + ], + "osteolytic defect of the phalanx of the toe": [ + "HP:0010177" + ], + "osteolytic defects of the phalanges of the toes": [ + "HP:0010177" + ], + "patchy sclerosis of toe phalanx": [ + "HP:0010178" + ], + "patchy sclerosis of the phalanx of the toe": [ + "HP:0010178" + ], + "patchy sclerosis of the phalanges of the toes": [ + "HP:0010178" + ], + "uneven increase in bone density in toe bone": [ + "HP:0010178" + ], + "symphalangism affect the phalanx of the toe": [ + "HP:0010179" + ], + "symphalangism affecting the phalanges of the toes": [ + "HP:0010179" + ], + "fuse toe bone": [ + "HP:0010179" + ], + "fused toe bones": [ + "HP:0010179" + ], + "triangular shape phalanx of the toe": [ + "HP:0010180" + ], + "triangular shaped phalanges of the toes": [ + "HP:0010180" + ], + "triangular shape toe bone": [ + "HP:0010180" + ], + "triangular shaped toe bones": [ + "HP:0010180" + ], + "duplication of phalanx of toe": [ + "HP:0010181" + ], + "duplicate toe bone": [ + "HP:0010181" + ], + "duplicated toe bone": [ + "HP:0010181" + ], + "partial / complete duplication of the phalanx of the toe": [ + "HP:0010181" + ], + "partial / complete duplication of the phalanges of the toes": [ + "HP:0010181" + ], + "abnormality of the distal phalanx of the toe": [ + "HP:0010182" + ], + "abnormality of the distal phalanges of the toes": [ + "HP:0010182" + ], + "abnormality of the outermost bone of the toe": [ + "HP:0010182" + ], + "abnormality of the outermost bone of the toes": [ + "HP:0010182" + ], + "abnormality of the middle phalanx of the toe": [ + "HP:0010183" + ], + "abnormality of the middle phalanges of the toes": [ + "HP:0010183" + ], + "abnormal middle bone of toe": [ + "HP:0010183" + ], + "abnormal middle bones of toe": [ + "HP:0010183" + ], + "abnormality of toe proximal phalanx": [ + "HP:0010184" + ], + "abnormal innermost toe bone": [ + "HP:0010184" + ], + "abnormality of the proximal phalanx of the toe": [ + "HP:0010184" + ], + "abnormality of the proximal phalanges of the toes": [ + "HP:0010184" + ], + "aplasia / hypoplasia of the distal phalanx of the toe": [ + "HP:0010185" + ], + "aplasia / hypoplasia of the distal phalanges of the toes": [ + "HP:0010185" + ], + "absent / hypoplastic terminal phalanx of toe": [ + "HP:0010185" + ], + "absent / hypoplastic terminal phalanges of toes": [ + "HP:0010185" + ], + "absent / small outermost bone of toe": [ + "HP:0010185" + ], + "absent / small outermost bones of toe": [ + "HP:0010185" + ], + "absent / underdevelop outermost bone of toe": [ + "HP:0010185" + ], + "absent / underdeveloped outermost bones of toe": [ + "HP:0010185" + ], + "hypoplasia / agenesis of distal phalanx of toe": [ + "HP:0010185" + ], + "hypoplasia / agenesis of distal phalanges of toes": [ + "HP:0010185" + ], + "broad distal phalanx of the toe": [ + "HP:0010186" + ], + "broad distal phalanx of the toes": [ + "HP:0010186" + ], + "broad outermost bone of the toe": [ + "HP:0010186" + ], + "wide outermost bone of the toe": [ + "HP:0010186" + ], + "bullet - shaped distal toe phalanx": [ + "HP:0010187" + ], + "bullet - shaped distal phalanx of the toe": [ + "HP:0010187" + ], + "bullet - shaped distal phalanges of the toes": [ + "HP:0010187" + ], + "bullet - shape outermost bone of the toe": [ + "HP:0010187" + ], + "bullet - shaped outermost bone of the toe": [ + "HP:0010187" + ], + "curve distal toe phalanx": [ + "HP:0010188" + ], + "curved distal toe phalanx": [ + "HP:0010188" + ], + "curve distal phalanx of the toe": [ + "HP:0010188" + ], + "curved distal phalanges of the toes": [ + "HP:0010188" + ], + "curve outermost bone of the toe": [ + "HP:0010188" + ], + "curved outermost bone of the toe": [ + "HP:0010188" + ], + "osteolytic defect of the distal phalanx of the toe": [ + "HP:0010189" + ], + "osteolytic defects of the distal phalanges of the toes": [ + "HP:0010189" + ], + "patchy sclerosis of distal toe phalanx": [ + "HP:0010190" + ], + "patchy sclerosis of the distal phalanx of the toe": [ + "HP:0010190" + ], + "patchy sclerosis of the distal phalanges of the toes": [ + "HP:0010190" + ], + "uneven increase in bone density in outermost toe bone": [ + "HP:0010190" + ], + "symphalangism affect the distal phalanx of the toe": [ + "HP:0010191" + ], + "symphalangism affecting the distal phalanges of the toes": [ + "HP:0010191" + ], + "fuse outermost bone of toe": [ + "HP:0010191" + ], + "fused outermost bones of toes": [ + "HP:0010191" + ], + "triangular shape distal phalanx of the toe": [ + "HP:0010192" + ], + "triangular shaped distal phalanges of the toes": [ + "HP:0010192" + ], + "triangular shape outermost bone of the toe": [ + "HP:0010192" + ], + "triangular shaped outermost bone of the toes": [ + "HP:0010192" + ], + "duplication of distal phalanx of toe": [ + "HP:0010193" + ], + "duplication of outermost bone of toe": [ + "HP:0010193" + ], + "partial / complete duplication of the distal phalanx of the toe": [ + "HP:0010193" + ], + "partial / complete duplication of the distal phalanges of the toes": [ + "HP:0010193" + ], + "aplasia / hypoplasia of the middle phalanx of the toe": [ + "HP:0010194" + ], + "aplasia / hypoplasia of the middle phalanges of the toes": [ + "HP:0010194" + ], + "absent / small middle bone of toe": [ + "HP:0010194" + ], + "absent / small middle bones of toe": [ + "HP:0010194" + ], + "absent / underdevelop middle bone of toe": [ + "HP:0010194" + ], + "absent / underdeveloped middle bones of toe": [ + "HP:0010194" + ], + "broad middle phalanx of the toe": [ + "HP:0010195" + ], + "broad middle phalanges of the toes": [ + "HP:0010195" + ], + "broad middle bone of the toe": [ + "HP:0010195" + ], + "broad middle bones of the toes": [ + "HP:0010195" + ], + "bullet - shape middle toe phalanx": [ + "HP:0010196" + ], + "bullet - shaped middle toe phalanx": [ + "HP:0010196" + ], + "bullet - shape middle bone of the toe": [ + "HP:0010196" + ], + "bullet - shaped middle bones of the toes": [ + "HP:0010196" + ], + "bullet - shape middle phalanx of the toe": [ + "HP:0010196" + ], + "bullet - shaped middle phalanges of the toes": [ + "HP:0010196" + ], + "curve middle toe phalanx": [ + "HP:0010197" + ], + "curved middle toe phalanx": [ + "HP:0010197" + ], + "curve middle bone of the toe": [ + "HP:0010197" + ], + "curved middle bones of the toes": [ + "HP:0010197" + ], + "curve middle phalanx of the toe": [ + "HP:0010197" + ], + "curved middle phalanges of the toes": [ + "HP:0010197" + ], + "osteolytic defect of the middle phalanx of the toe": [ + "HP:0010198" + ], + "osteolytic defects of the middle phalanges of the toes": [ + "HP:0010198" + ], + "patchy sclerosis of middle toe phalanx": [ + "HP:0010199" + ], + "patchy sclerosis of the middle phalanx of the toe": [ + "HP:0010199" + ], + "patchy sclerosis of the middle phalanges of the toes": [ + "HP:0010199" + ], + "uneven increase in bone density in middle toe bone": [ + "HP:0010199" + ], + "symphalangism affect the middle phalanx of the toe": [ + "HP:0010200" + ], + "symphalangism affecting the middle phalanges of the toes": [ + "HP:0010200" + ], + "fuse middle bone of toe": [ + "HP:0010200" + ], + "fused middle bones of toes": [ + "HP:0010200" + ], + "triangular shape middle phalanx of the toe": [ + "HP:0010201" + ], + "triangular shaped middle phalanges of the toes": [ + "HP:0010201" + ], + "triangular shape middle bone of toe": [ + "HP:0010201" + ], + "triangular shaped middle bones of toes": [ + "HP:0010201" + ], + "duplication of middle phalanx of toe": [ + "HP:0010202" + ], + "partial / complete duplication of the middle bone of the toe": [ + "HP:0010202" + ], + "partial / complete duplication of the middle bones of the toes": [ + "HP:0010202" + ], + "partial / complete duplication of the middle phalanx of the toe": [ + "HP:0010202" + ], + "partial / complete duplication of the middle phalanges of the toes": [ + "HP:0010202" + ], + "aplasia / hypoplasia of proximal toe phalanx": [ + "HP:0010203" + ], + "absent / small innermost toe bone": [ + "HP:0010203" + ], + "absent / small innermost toe bones": [ + "HP:0010203" + ], + "absent / underdevelop innermost toe bone": [ + "HP:0010203" + ], + "absent / underdeveloped innermost toe bones": [ + "HP:0010203" + ], + "aplasia / hypoplasia of the proximal phalanx of the toe": [ + "HP:0010203" + ], + "aplasia / hypoplasia of the proximal phalanges of the toes": [ + "HP:0010203" + ], + "broad proximal phalanx of toe": [ + "HP:0010204" + ], + "broad innermost toe bone": [ + "HP:0010204" + ], + "bullet - shape proximal toe phalanx": [ + "HP:0010205" + ], + "bullet - shaped proximal toe phalanx": [ + "HP:0010205" + ], + "bullet - shape innermost toe bone": [ + "HP:0010205" + ], + "bullet - shaped innermost toe bone": [ + "HP:0010205" + ], + "bullet - shape proximal phalanx of the toe": [ + "HP:0010205" + ], + "bullet - shaped proximal phalanges of the toes": [ + "HP:0010205" + ], + "bullet - shape proximal phalanx of toe": [ + "HP:0010205" + ], + "bullet - shaped proximal phalanges of toe": [ + "HP:0010205" + ], + "curve proximal toe phalanx": [ + "HP:0010206" + ], + "curved proximal toe phalanx": [ + "HP:0010206" + ], + "curve innermost toe bone": [ + "HP:0010206" + ], + "curved innermost toe bones": [ + "HP:0010206" + ], + "curve proximal phalanx of the toe": [ + "HP:0010206" + ], + "curved proximal phalanges of the toes": [ + "HP:0010206" + ], + "osteolytic defect of the proximal toe phalanx": [ + "HP:0010207" + ], + "osteolytic defect of the proximal phalanx of the toe": [ + "HP:0010207" + ], + "osteolytic defects of the proximal phalanges of the toes": [ + "HP:0010207" + ], + "patchy sclerosis of proximal toe phalanx": [ + "HP:0010208" + ], + "patchy sclerosis of the proximal phalanx of the toe": [ + "HP:0010208" + ], + "patchy sclerosis of the proximal phalanges of the toes": [ + "HP:0010208" + ], + "uneven increase in bone density in innermost toe bone": [ + "HP:0010208" + ], + "symphalangism affect the proximal phalanx of the toe": [ + "HP:0010209" + ], + "symphalangism affecting the proximal phalanges of the toes": [ + "HP:0010209" + ], + "fuse innermost bone of toe": [ + "HP:0010209" + ], + "fused innermost bones of toes": [ + "HP:0010209" + ], + "triangular shape proximal phalanx of the toe": [ + "HP:0010210" + ], + "triangular shaped proximal phalanges of the toes": [ + "HP:0010210" + ], + "triangular shape innermost toe bone": [ + "HP:0010210" + ], + "triangular shaped innermost toe bones": [ + "HP:0010210" + ], + "duplication of proximal phalanx of toe": [ + "HP:0010211" + ], + "duplication of innermost toe bone": [ + "HP:0010211" + ], + "duplication of innermost toe bones": [ + "HP:0010211" + ], + "partial / complete duplication of the proximal phalanx of the toe": [ + "HP:0010211" + ], + "partial / complete duplication of the proximal phalanges of the toes": [ + "HP:0010211" + ], + "flexion contracture of the hallux": [ + "HP:0010212" + ], + "joint contracture of the big toe": [ + "HP:0010212" + ], + "joint contracture of the hallux": [ + "HP:0010212" + ], + "contracture of the tarsometatarsal joint of the hallux": [ + "HP:0010213" + ], + "contracture of the interphalangeal joint of the hallux": [ + "HP:0010214" + ], + "contracture of the metatarsophalangeal joint of the hallux": [ + "HP:0010215" + ], + "contractures of the metatarsophalangeal joint of the hallux": [ + "HP:0010215" + ], + "structural foot deformity": [ + "HP:0010219" + ], + "abnormality of the epiphysis of the 2nd metacarpal": [ + "HP:0010220" + ], + "abnormality of the end part of the 2nd long bone of hand": [ + "HP:0010220" + ], + "obsolete pseudoepiphysis of the 2nd metacarpal": [ + "HP:0010221" + ], + "abnormality of the epiphysis of the 3rd metacarpal": [ + "HP:0010222" + ], + "abnormality of the end part of the 3rd long bone of hand": [ + "HP:0010222" + ], + "pseudoepiphysis of the 3rd metacarpal": [ + "HP:0010223" + ], + "abnormality of the epiphysis of the 4th metacarpal": [ + "HP:0010224" + ], + "abnormality of the end part of the 4th long bone of hand": [ + "HP:0010224" + ], + "pseudoepiphysis of the 4th metacarpal": [ + "HP:0010225" + ], + "abnormality of the epiphysis of the 5th metacarpal": [ + "HP:0010226" + ], + "abnormality of the end part of the long bone of little finger": [ + "HP:0010226" + ], + "abnormality of the end part of the long bone of pinkie finger": [ + "HP:0010226" + ], + "abnormality of the end part of the long bone of pinky finger": [ + "HP:0010226" + ], + "pseudoepiphysis of the 5th metacarpal": [ + "HP:0010227" + ], + "absent epiphysis of the phalanx of the hand": [ + "HP:0010228" + ], + "absent epiphyses of the phalanges of the hand": [ + "HP:0010228" + ], + "absent end part of finger": [ + "HP:0010228" + ], + "absent end part of fingers": [ + "HP:0010228" + ], + "absent epiphysis of the finger": [ + "HP:0010228" + ], + "absent epiphyses of the fingers": [ + "HP:0010228" + ], + "bracket epiphysis of the phalanx of the hand": [ + "HP:0010229" + ], + "bracket epiphyses of the phalanges of the hand": [ + "HP:0010229" + ], + "bracket epiphysis of the finger": [ + "HP:0010229" + ], + "bracket epiphyses of the fingers": [ + "HP:0010229" + ], + "bracket shape end part of finger bone": [ + "HP:0010229" + ], + "bracket shaped end part of finger bones": [ + "HP:0010229" + ], + "cone - shaped epiphysis of the phalanx of the hand": [ + "HP:0010230" + ], + "cone - shaped epiphyses of the phalanges of the hand": [ + "HP:0010230" + ], + "cone - shaped end part of finger bone": [ + "HP:0010230" + ], + "cone - shaped end part of finger bones": [ + "HP:0010230" + ], + "cone - shaped epiphysis of hand": [ + "HP:0010230" + ], + "cone - shaped epiphyses of hand": [ + "HP:0010230" + ], + "cone - shaped epiphysis of phalanx": [ + "HP:0010230" + ], + "cone - shaped epiphyses of phalanges": [ + "HP:0010230" + ], + "cone - shaped epiphysis of the finger": [ + "HP:0010230" + ], + "cone - shaped epiphyses of the fingers": [ + "HP:0010230" + ], + "cone - shaped phalangeal epiphysis": [ + "HP:0010230" + ], + "cone - shaped phalangeal epiphyses": [ + "HP:0010230" + ], + "con epiphysis": [ + "HP:0010230" + ], + "coned epiphyses": [ + "HP:0010230" + ], + "coned epiphysis of hand": [ + "HP:0010230" + ], + "coned epiphyses of hands": [ + "HP:0010230" + ], + "conical phalangeal epiphysis": [ + "HP:0010230" + ], + "conical phalangeal epiphyses": [ + "HP:0010230" + ], + "phalangeal cone - shaped epiphysis": [ + "HP:0010230" + ], + "phalangeal cone - shaped epiphyses": [ + "HP:0010230" + ], + "enlarged epiphysis of the phalanx of the hand": [ + "HP:0010231" + ], + "enlarged epiphyses of the phalanges of the hand": [ + "HP:0010231" + ], + "enlarged end part of finger bone": [ + "HP:0010231" + ], + "enlarged end part of finger bones": [ + "HP:0010231" + ], + "enlarged epiphysis of the finger": [ + "HP:0010231" + ], + "enlarged epiphyses of the fingers": [ + "HP:0010231" + ], + "enlarge phalangeal epiphysis": [ + "HP:0010231" + ], + "enlarged phalangeal epiphyses": [ + "HP:0010231" + ], + "fragmentation of the epiphysis of the phalanx of the hand": [ + "HP:0010232" + ], + "fragmentation of the epiphyses of the phalanges of the hand": [ + "HP:0010232" + ], + "fragmentation of end part of finger bone": [ + "HP:0010232" + ], + "fragmentation of end part of finger bones": [ + "HP:0010232" + ], + "fragmentation of the epiphysis of the finger": [ + "HP:0010232" + ], + "fragmentation of the epiphyses of the fingers": [ + "HP:0010232" + ], + "irregular epiphysis of the phalanx of the hand": [ + "HP:0010233" + ], + "irregular epiphyses of the phalanges of the hand": [ + "HP:0010233" + ], + "irregular end part of finger bone": [ + "HP:0010233" + ], + "irregular end part of finger bones": [ 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"HP:0010236" + ], + "small epiphyses of the phalanges of the hand": [ + "HP:0010236" + ], + "small end part of finger bone": [ + "HP:0010236" + ], + "small end part of finger bones": [ + "HP:0010236" + ], + "small epiphysis of the finger": [ + "HP:0010236" + ], + "small epiphyses of the fingers": [ + "HP:0010236" + ], + "epiphyseal stippling of finger phalanx": [ + "HP:0010237" + ], + "epiphyseal stippling of finger phalanges": [ + "HP:0010237" + ], + "speckled calcification in end part of finger bone": [ + "HP:0010237" + ], + "speckled calcifications in end part of finger bones": [ + "HP:0010237" + ], + "stippling of the epiphysis of the finger": [ + "HP:0010237" + ], + "stippling of the epiphyses of the fingers": [ + "HP:0010237" + ], + "stippling of the epiphysis of the phalanx of the hand": [ + "HP:0010237" + ], + "stippling of the epiphyses of the phalanges of the hand": [ + "HP:0010237" + ], + "triangular epiphysis of the phalanx of the hand": [ + "HP:0010238" + ], + "triangular epiphyses of the phalanges of the hand": [ + "HP:0010238" + ], + "delta - shaped epiphysis of the finger": [ + "HP:0010238" + ], + "delta - shaped epiphyses of the fingers": [ + "HP:0010238" + ], + "triangular end part of finger bone": [ + "HP:0010238" + ], + "triangular end part of finger bones": [ + "HP:0010238" + ], + "triangular epiphysis of the finger": [ + "HP:0010238" + ], + "triangular epiphyses of the fingers": [ + "HP:0010238" + ], + "aplasia of the middle phalanx of the hand": [ + "HP:0010239" + ], + "absent middle bone of hand": [ + "HP:0010239" + ], + "absent middle bones of hand": [ + "HP:0010239" + ], + "absent middle phalanx": [ + "HP:0010239" + ], + "absent middle phalanges": [ + "HP:0010239" + ], + "miss middle phalanx": [ + "HP:0010239" + ], + "missing middle phalanges": [ + "HP:0010239" + ], + "short proximal phalanx of finger": [ + "HP:0010241" + ], + "hypoplasia of the proximal phalanx of the hand": [ + "HP:0010241" + ], + "hypoplasia of the proximal phalanges of the hand": [ + "HP:0010241" + ], + "short innermost finger bone": [ + "HP:0010241" + ], + "short innermost finger bones": [ + "HP:0010241" + ], + "short proximal phalanx": [ + "HP:0010241" + ], + "short proximal phalanges": [ + "HP:0010241" + ], + "shorten in proximal phalanx": [ + "HP:0010241" + ], + "shortening in proximal phalanges": [ + "HP:0010241" + ], + "aplasia of the proximal phalanx of the hand": [ + "HP:0010242" + ], + "aplasia of the proximal phalanges of the hand": [ + "HP:0010242" + ], + "absent innermost bone": [ + "HP:0010242" + ], + "absent innermost bones": [ + "HP:0010242" + ], + "absent proximal phalanx": [ + "HP:0010242" + ], + "absent proximal phalanges": [ + "HP:0010242" + ], + "abnormality of the epiphysis of the distal phalanx of finger": [ + "HP:0010243" + ], + "abnormality of the epiphyses of the distal phalanx of finger": [ + "HP:0010243" + ], + "abnormality of the end part of the outermost bone of finger": [ + "HP:0010243" + ], + "abnormality of the epiphysis of the middle phalanx of the hand": [ + "HP:0010244" + ], + "abnormality of the epiphyses of the middle phalanges of the hand": [ + "HP:0010244" + ], + "abnormality of the end part of the middle hand bone": [ + "HP:0010244" + ], + "abnormality of the end part of the middle hand bones": [ + "HP:0010244" + ], + "abnormality of the epiphysis of the proximal phalanx of the hand": [ + "HP:0010245" + ], + "abnormality of the epiphyses of the proximal phalanges of the hand": [ + "HP:0010245" + ], + "abnormality of the end part of the innermost hand bone": [ + "HP:0010245" + ], + "abnormality of the end part of the innermost hand bones": [ + "HP:0010245" + ], + "absent epiphysis of the distal phalanx of the hand": [ + "HP:0010246" + ], + "absent epiphyses of the distal phalanges of the hand": [ + "HP:0010246" + ], + "absent end part of the outermost hand bone": [ + "HP:0010246" + ], + "absent end part of the outermost hand bones": [ + "HP:0010246" + ], + "bracket epiphysis of the distal phalanx of the hand": [ + "HP:0010247" + ], + "bracket epiphyses of the distal phalanges of the hand": [ + "HP:0010247" + ], + "bracket shape end part of the outermost hand bone": [ + "HP:0010247" + ], + "bracket shaped end part of the outermost hand bones": [ + "HP:0010247" + ], + "cone - shaped epiphysis of the distal phalanx of the hand": [ + "HP:0010248" + ], + "cone - shaped epiphyses of the distal phalanges of the hand": [ + "HP:0010248" + ], + "cone - shaped end part of the outermost hand bone": [ + "HP:0010248" + ], + "cone - shaped end part of the outermost hand bones": [ + "HP:0010248" + ], + "enlarged epiphysis of the distal phalanx of the hand": [ + "HP:0010249" + ], + "enlarged epiphyses of the distal phalanges of the hand": [ + "HP:0010249" + ], + "enlarged end part of the outermost hand bone": [ + "HP:0010249" + ], + "enlarged end part of the outermost hand bones": [ + "HP:0010249" + ], + "fragmentation of the epiphysis of the distal phalanx of the hand": [ + "HP:0010250" + ], + "fragmentation of the epiphyses of the distal phalanges of the hand": [ + "HP:0010250" + ], + "fragmentation of the end part of the outermost hand bone": [ + "HP:0010250" + ], + "fragmentation of the end part of the outermost hand bones": [ + "HP:0010250" + ], + "irregular epiphysis of the distal phalanx of the hand": [ + "HP:0010251" + ], + "irregular epiphyses of the distal phalanges of the hand": [ + "HP:0010251" + ], + "irregular end part of the outermost hand bone": [ + "HP:0010251" + ], + "irregular end part of the outermost hand bones": [ + "HP:0010251" + ], + "ivory epiphysis of the distal phalanx of the hand": [ + "HP:0010252" + ], + "ivory epiphyses of the distal phalanges of the hand": [ + "HP:0010252" + ], + "eburnated epiphysis of distal phalanx": [ + "HP:0010252" + ], + "eburnated epiphyses of distal phalanges": [ + "HP:0010252" + ], + "increase bone density of end part of the outermost hand bone": [ + "HP:0010252" + ], + "increased bone density of end part of the outermost hand bones": [ + "HP:0010252" + ], + "pseudoepiphyses of the distal phalanx of the hand": [ + "HP:0010253" + ], + "pseudoepiphyses of the distal phalanges of the hand": [ + "HP:0010253" + ], + "small epiphysis of the distal phalanx of the hand": [ + "HP:0010254" + ], + "small epiphyses of the distal phalanges of the hand": [ + "HP:0010254" + ], + "small end part of the outermost hand bone": [ + "HP:0010254" + ], + "small end part of the outermost hand bones": [ + "HP:0010254" + ], + "stippling of the epiphysis of the distal phalanx of the hand": [ + "HP:0010255" + ], + "stippling of the epiphyses of the distal phalanges of the hand": [ + "HP:0010255" + ], + "speckled calcification in the end part of the outermost hand bone": [ + "HP:0010255" + ], + "speckled calcifications in the end part of the outermost hand bones": [ + "HP:0010255" + ], + "triangular epiphysis of the distal phalanx of the hand": [ + "HP:0010256" + ], + "triangular epiphyses of the distal phalanges of the hand": [ + "HP:0010256" + ], + "triangular end part of the outermost hand bone": [ + "HP:0010256" + ], + "triangular end part of the outermost hand bones": [ + "HP:0010256" + ], + "absent epiphysis of the middle phalanx of the hand": [ + "HP:0010257" + ], + "absent epiphyses of the middle phalanges of the hand": [ + "HP:0010257" + ], + "absent end part of the middle hand bone": [ + "HP:0010257" + ], + "absent end part of the middle hand bones": [ + "HP:0010257" + ], + "bracket epiphysis of the middle phalanx of the hand": [ + "HP:0010258" + ], + "bracket epiphyses of the middle phalanges of the hand": [ + "HP:0010258" + ], + "bracket shape end part of the middle hand bone": [ + "HP:0010258" + ], + "bracket shaped end part of the middle hand bones": [ + "HP:0010258" + ], + "cone - shaped epiphysis of the middle phalanx of the hand": [ + "HP:0010259" + ], + "cone - shaped epiphyses of the middle phalanges of the hand": [ + "HP:0010259" + ], + "cone - shaped end part of the middle hand bone": [ + "HP:0010259" + ], + "cone - shaped end part of the middle hand bones": [ + "HP:0010259" + ], + "cone - shaped epiphysis of middle phalanx": [ + "HP:0010259" + ], + "cone - shaped epiphyses of middle phalanges": [ + "HP:0010259" + ], + "enlarged epiphysis of the middle phalanx of the hand": [ + "HP:0010260" + ], + "enlarged epiphyses of the middle phalanges of the hand": [ + "HP:0010260" + ], + "enlarged end part of the middle hand bone": [ + "HP:0010260" + ], + "enlarged end part of the middle hand bones": [ + "HP:0010260" + ], + "fragmentation of the epiphysis of the middle phalanx of the hand": [ + "HP:0010261" + ], + "fragmentation of the epiphyses of the middle phalanges of the hand": [ + "HP:0010261" + ], + "fragmentation of the end part of the middle hand bone": [ + "HP:0010261" + ], + "fragmentation of the end part of the middle hand bones": [ + "HP:0010261" + ], + "irregular epiphysis of the middle phalanx of the hand": [ + "HP:0010262" + ], + "irregular epiphyses of the middle phalanges of the hand": [ + "HP:0010262" + ], + "irregular end part of middle hand bone": [ + "HP:0010262" + ], + "irregular end part of middle hand bones": [ + "HP:0010262" + ], + "ivory epiphysis of the middle phalanx of the hand": [ + "HP:0010263" + ], + "ivory epiphyses of the middle phalanges of the hand": [ + "HP:0010263" + ], + "increase bone density of end part of the middle hand bone": [ + "HP:0010263" + ], + "increased bone density of end part of the middle hand bones": [ + "HP:0010263" + ], + "pseudoepiphyses of the middle phalanx of the hand": [ + "HP:0010264" + ], + "pseudoepiphyses of the middle phalanges of the hand": [ + "HP:0010264" + ], + "small epiphysis of the middle phalanx of the hand": [ + "HP:0010265" + ], + "small epiphyses of the middle phalanges of the hand": [ + "HP:0010265" + ], + "small end part of the middle hand bone": [ + "HP:0010265" + ], + "small end part of the middle hand bones": [ + "HP:0010265" + ], + "stippling of the epiphysis of the middle phalanx of the hand": [ + "HP:0010266" + ], + "stippling of the epiphyses of the middle phalanges of the hand": [ + "HP:0010266" + ], + "speckled calcification in the end part of the middle hand bone": [ + "HP:0010266" + ], + "speckled calcifications in the end part of the middle hand bones": [ + "HP:0010266" + ], + "triangular epiphysis of the middle phalanx of the hand": [ + "HP:0010267" + ], + "triangular epiphyses of the middle phalanges of the hand": [ + "HP:0010267" + ], + "triangular end part of the middle hand bone": [ + "HP:0010267" + ], + "triangular end part of the middle hand bones": [ + "HP:0010267" + ], + "absent epiphysis of the proximal phalanx of the hand": [ + "HP:0010268" + ], + "absent epiphyses of the proximal phalanges of the hand": [ + "HP:0010268" + ], + "absent end part of the innermost hand bone": [ + "HP:0010268" + ], + "absent end part of the innermost hand bones": [ + "HP:0010268" + ], + "bracket epiphysis of the proximal phalanx of the hand": [ + "HP:0010269" + ], + "bracket epiphyses of the proximal phalanges of the hand": [ + "HP:0010269" + ], + "bracket shape end part of the innermost hand bone": [ + "HP:0010269" + ], + "bracket shaped end part of the innermost hand bones": [ + "HP:0010269" + ], + "cone - shaped epiphysis of the proximal phalanx of the hand": [ + "HP:0010270" + ], + "cone - shaped epiphyses of the proximal phalanges of the hand": [ + "HP:0010270" + ], + "cone - shaped end part of the innermost hand bone": [ + "HP:0010270" + ], + "cone - shaped end part of the innermost hand bones": [ + "HP:0010270" + ], + "enlarged epiphysis of the proximal phalanx of the hand": [ + "HP:0010271" + ], + "enlarged epiphyses of the proximal phalanges of the hand": [ + "HP:0010271" + ], + "enlarged end part of the innermost hand bone": [ + "HP:0010271" + ], + "enlarged end part of the innermost hand bones": [ + "HP:0010271" + ], + "fragmentation of the epiphysis of the proximal phalanx of the hand": [ + "HP:0010272" + ], + "fragmentation of the epiphyses of the proximal phalanges of the hand": [ + "HP:0010272" + ], + "fragmentation of the end part of the innermost hand bone": [ + "HP:0010272" + ], + "fragmentation of the end part of the innermost hand bones": [ + "HP:0010272" + ], + "irregular epiphysis of the proximal phalanx of the hand": [ + "HP:0010273" + ], + "irregular epiphyses of the proximal phalanges of the hand": [ + "HP:0010273" + ], + "irregular end part of the innermost hand bone": [ + "HP:0010273" + ], + "irregular end part of the innermost hand bones": [ + "HP:0010273" + ], + "ivory epiphysis of the proximal phalanx of the hand": [ + "HP:0010274" + ], + "ivory epiphyses of the proximal phalanges of the hand": [ + "HP:0010274" + ], + "increase bone density of end part of the innermost hand bone": [ + "HP:0010274" + ], + "increased bone density of end part of the innermost hand bones": [ + "HP:0010274" + ], + "pseudoepiphyses of the proximal phalanx of the hand": [ + "HP:0010275" + ], + "pseudoepiphyses of the proximal phalanges of the hand": [ + "HP:0010275" + ], + "small epiphysis of the proximal phalanx of the hand": [ + "HP:0010276" + ], + "small epiphyses of the proximal phalanges of the hand": [ + "HP:0010276" + ], + "small end part of the innermost hand bone": [ + "HP:0010276" + ], + "small end part of the innermost hand bones": [ + "HP:0010276" + ], + "stippling of the epiphysis of the proximal phalanx of the hand": [ + "HP:0010277" + ], + "stippling of the epiphyses of the proximal phalanges of the hand": [ + "HP:0010277" + ], + "speckled calcification in the end part of the innermost hand bone": [ + "HP:0010277" + ], + "speckled calcifications in the end part of the innermost hand bones": [ + "HP:0010277" + ], + "triangular epiphysis of the proximal phalanx of the hand": [ + "HP:0010278" + ], + "triangular epiphyses of the proximal phalanges of the hand": [ + "HP:0010278" + ], + "triangular end part of the innermost hand bone": [ + "HP:0010278" + ], + "triangular end part of the innermost hand bones": [ + "HP:0010278" + ], + "stomatitis": [ + "HP:0010280" + ], + "gingivostomatitis": [ + "HP:0010280" + ], + "inflammation of the mouth": [ + "HP:0010280" + ], + "cleft lower lip": [ + "HP:0010281" + ], + "cleft of the low lip": [ + "HP:0010281" + ], + "cleft of the lower lip": [ + "HP:0010281" + ], + "low labial cleft": [ + "HP:0010281" + ], + "lower labial cleft": [ + "HP:0010281" + ], + "thin low lip vermilion": [ + "HP:0010282" + ], + "thin lower lip vermilion": [ + "HP:0010282" + ], + "decreased height of low lip vermilion": [ + "HP:0010282" + ], + "decreased height of lower lip vermilion": [ + "HP:0010282" + ], + "decreased volume of low lip": [ + "HP:0010282" + ], + "decreased volume of lower lip": [ + "HP:0010282" + ], + "decreased volume of low lip vermilion": [ + "HP:0010282" + ], + "decreased volume of lower lip vermilion": [ + "HP:0010282" + ], + "thin low lip": [ + "HP:0010282" + ], + "thin lower lip": [ + "HP:0010282" + ], + "thin red part of the low lip": [ + "HP:0010282" + ], + "thin red part of the lower lip": [ + "HP:0010282" + ], + "thin vermilion border of low lip": [ + "HP:0010282" + ], + "thin vermilion border of lower lip": [ + "HP:0010282" + ], + "intra - oral hyperpigmentation": [ + "HP:0010284" + ], + "dark color of gum": [ + "HP:0010284" + ], + "dark color of gums": [ + "HP:0010284" + ], + "dark colour of gum": [ + "HP:0010284" + ], + "dark colour of gums": [ + "HP:0010284" + ], + "gingival hyperpigmentation": [ + "HP:0010284" + ], + "gingival melanin pigmentation": [ + "HP:0010284" + ], + "hyperpigmentation of oral mucosa": [ + "HP:0010284" + ], + "oral mucosa melanin pigmentation": [ + "HP:0010284" + ], + "oral racial pigmentation": [ + "HP:0010284" + ], + "pigment gum": [ + "HP:0010284" + ], + "pigmented gums": [ + "HP:0010284" + ], + "oral synechia": [ + "HP:0010285" + ], + "oral fibrous band": [ + "HP:0010285" + ], + "oral fibrous bands": [ + "HP:0010285" + ], + "synechiae of the mouth": [ + "HP:0010285" + ], + "abnormal salivary gland morphology": [ + "HP:0010286" + ], + "abnormality of the salivary gland": [ + "HP:0010286" + ], + "abnormality of the salivary glands": [ + "HP:0010286" + ], + "salivary gland disease": [ + "HP:0010286" + ], + "abnormality of the submandibular gland": [ + "HP:0010287" + ], + "abnormality of the submandibular glands": [ + "HP:0010287" + ], + "abnormality of the submaxillary gland": [ + "HP:0010287" + ], + "abnormality of the submaxillary glands": [ + "HP:0010287" + ], + "abnormality of the sublingual gland": [ + "HP:0010288" + ], + "abnormality of the sublingual glands": [ + "HP:0010288" + ], + "cleft of alveolar ridge of maxilla": [ + "HP:0010289" + ], + "alveolar ridge cleft": [ + "HP:0010289" + ], + "cleft of alveolar process": [ + "HP:0010289" + ], + "cleft of gum ridge": [ + "HP:0010289" + ], + "notch of alveolar process": [ + "HP:0010289" + ], + "notch of alveolar ridge": [ + "HP:0010289" + ], + "notch of gum ridge": [ + "HP:0010289" + ], + "short hard palate": [ + "HP:0010290" + ], + "decreased length of hard palate": [ + "HP:0010290" + ], + "hypoplastic palate": [ + "HP:0010290" + ], + "short palate": [ + "HP:0010290" + ], + "prominent palatine ridge": [ + "HP:0010291" + ], + "prominent palatine ridges": [ + "HP:0010291" + ], + "large lateral palatal fold": [ + "HP:0010291" + ], + "large lateral palatal folds": [ + "HP:0010291" + ], + "large lateral palatal ridge": [ + "HP:0010291" + ], + "large lateral palatal ridges": [ + "HP:0010291" + ], + "prominent lateral palatal fold": [ + "HP:0010291" + ], + "prominent lateral palatal folds": [ + "HP:0010291" + ], + "prominent lateral palatal ridge": [ + "HP:0010291" + ], + "prominent lateral palatal ridges": [ + "HP:0010291" + ], + "prominent palatine fold": [ + "HP:0010291" + ], + "prominent palatine folds": [ + "HP:0010291" + ], + "absent uvula": [ + "HP:0010292" + ], + "absent palatine uvula": [ + "HP:0010292" + ], + "agenesis of uvula": [ + "HP:0010292" + ], + "congenital absence of uvula": [ + "HP:0010292" + ], + "miss uvula": [ + "HP:0010292" + ], + "missing uvula": [ + "HP:0010292" + ], + "uvula aplasia": [ + "HP:0010292" + ], + "aplasia / hypoplasia of the uvula": [ + "HP:0010293" + ], + "aplasia / hypoplasia of palatine uvula": [ + "HP:0010293" + ], + "palate fistula": [ + "HP:0010294" + ], + "hole in roof of mouth": [ + "HP:0010294" + ], + "palatal hole": [ + "HP:0010294" + ], + "palatal perforation": [ + "HP:0010294" + ], + "aplasia / hypoplasia of the tongue": [ + "HP:0010295" + ], + "lingual aplasia / hypoplasia": [ + "HP:0010295" + ], + "ankyloglossia": [ + "HP:0010296" + ], + "tongue tie": [ + "HP:0010296" + ], + "tongue tied": [ + "HP:0010296" + ], + "bifid tongue": [ + "HP:0010297" + ], + "bifurcate tongue": [ + "HP:0010297" + ], + "bifurcated tongue": [ + "HP:0010297" + ], + "bilobed tongue": [ + "HP:0010297" + ], + "cleft tongue": [ + "HP:0010297" + ], + "fork tongue": [ + "HP:0010297" + ], + "forked tongue": [ + "HP:0010297" + ], + "snake tongue": [ + "HP:0010297" + ], + "split tongue": [ + "HP:0010297" + ], + "smooth tongue": [ + "HP:0010298" + ], + "atrophy of dorsum of tongue": [ + "HP:0010298" + ], + "atrophy of lingual surface": [ + "HP:0010298" + ], + "atrophy of tongue surface": [ + "HP:0010298" + ], + "smooth dorsum of tongue": [ + "HP:0010298" + ], + "smooth lingual surface": [ + "HP:0010298" + ], + "smooth surface of tongue": [ + "HP:0010298" + ], + "abnormal dentin morphology": [ + "HP:0010299" + ], + "abnormal dentin": [ + "HP:0010299" + ], + "abnormality of dentin": [ + "HP:0010299" + ], + "abnormality of dentine": [ + "HP:0010299" + ], + "dentin anomaly": [ + "HP:0010299" + ], + "abnormally low - pitch voice": [ + "HP:0010300" + ], + "abnormally low - pitched voice": [ + "HP:0010300" + ], + "spinal dysraphism": [ + "HP:0010301" + ], + "incomplete closure of the vertebral arch": [ + "HP:0010301" + ], + "spinal cord tumor": [ + "HP:0010302" + ], + "spinal cord tumour": [ + "HP:0010302" + ], + "spinal tumor": [ + "HP:0010302" + ], + "spinal tumors": [ + "HP:0010302" + ], + "spinal tumour": [ + "HP:0010302" + ], + "spinal tumours": [ + "HP:0010302" + ], + "tumor of the spinal cord": [ + "HP:0010302" + ], + "tumour of the spinal cord": [ + "HP:0010302" + ], + "abnormal spinal meningeal morphology": [ + "HP:0010303" + ], + "abnormality of the spinal meninges": [ + "HP:0010303" + ], + "spinal meningeal diverticulum": [ + "HP:0010304" + ], + "absence of the sacrum": [ + "HP:0010305" + ], + "absent sacrum": [ + "HP:0010305" + ], + "sacral agenesis": [ + "HP:0010305" + ], + "sacrococcygeal agenesis": [ + "HP:0010305" + ], + "short thorax": [ + "HP:0010306" + ], + "short than typical length between neck and abdomen": [ + "HP:0010306" + ], + "shorter than typical length between neck and abdomen": [ + "HP:0010306" + ], + "stridor": [ + "HP:0010307" + ], + "noisy breathe": [ + "HP:0010307" + ], + "noisy breathing": [ + "HP:0010307" + ], + "asternia": [ + "HP:0010308" + ], + "aplasia of the sternum": [ + "HP:0010308" + ], + "breast bone aplasia": [ + "HP:0010308" + ], + "bifid sternum": [ + "HP:0010309" + ], + "sternal cleft": [ + "HP:0010309" + ], + "chylothorax": [ + "HP:0010310" + ], + "aplasia / hypoplasia of the breast": [ + "HP:0010311" + ], + "aplasia / hypoplasia of the breasts": [ + "HP:0010311" + ], + "absent / small breast": [ + "HP:0010311" + ], + "absent / small breasts": [ + "HP:0010311" + ], + "absent / underdevelop breast": [ + "HP:0010311" + ], + "absent / underdeveloped breasts": [ + "HP:0010311" + ], + "asymmetry of the breast": [ + "HP:0010312" + ], + "asymmetry of the breasts": [ + "HP:0010312" + ], + "breast hypertrophy": [ + "HP:0010313" + ], + "breast enlargement": [ + "HP:0010313" + ], + "breast enlarge": [ + "HP:0010313" + ], + "breasts enlarged": [ + "HP:0010313" + ], + "gigantomastia": [ + "HP:0010313" + ], + "hypertrophy of the breast": [ + "HP:0010313" + ], + "hypertrophy of the breasts": [ + "HP:0010313" + ], + "large breast": [ + "HP:0010313" + ], + "macromastia": [ + "HP:0010313" + ], + "premature thelarche": [ + "HP:0010314" + ], + "premature breast development": [ + "HP:0010314" + ], + "aplasia / hypoplasia of the diaphragm": [ + "HP:0010315" + ], + "absent / small diaprhagm": [ + "HP:0010315" + ], + "absent / underdevelop diaprhagm": [ + "HP:0010315" + ], + "absent / underdeveloped diaprhagm": [ + "HP:0010315" + ], + "ebstein anomaly of the tricuspid valve": [ + "HP:0010316" + ], + "ebstein 's anomaly": [ + "HP:0010316" + ], + "ebstein 's anomaly of the tricuspid valve": [ + "HP:0010316" + ], + "ebstein 's malformation": [ + "HP:0010316" + ], + "scapular aplasia": [ + "HP:0010317" + ], + "absent scapula": [ + "HP:0010317" + ], + "absent shoulder blade": [ + "HP:0010317" + ], + "aplasia / hypoplasia of the abdominal wall musculature": [ + "HP:0010318" + ], + "absent / small abdominal wall muscle": [ + "HP:0010318" + ], + "absent / small abdominal wall muscles": [ + "HP:0010318" + ], + "absent / underdevelop abdominal wall muscle": [ + "HP:0010318" + ], + "absent / underdeveloped abdominal wall muscles": [ + "HP:0010318" + ], + "abnormality of the 2nd toe": [ + "HP:0010319" + ], + "abnormality of the 3rd toe": [ + "HP:0010320" + ], + "abnormality of the 4th toe": [ + "HP:0010321" + ], + "abnormality of the 5th toe": [ + "HP:0010322" + ], + "abnormality of the little toe": [ + "HP:0010322" + ], + "abnormality of the pinkie toe": [ + "HP:0010322" + ], + "abnormality of the pinky toe": [ + "HP:0010322" + ], + "abnormality of the epiphysis of the 2nd toe": [ + "HP:0010323" + ], + "abnormality of the epiphyses of the 2nd toe": [ + "HP:0010323" + ], + "abnormality of the end part of the 2nd toe bone": [ + "HP:0010323" + ], + "abnormal morphology of phalanx of the 2nd toe": [ + "HP:0010324" + ], + "abnormality of the 2nd toe bone": [ + "HP:0010324" + ], + "aplasia / hypoplasia of the 2nd toe": [ + "HP:0010325" + ], + "absent / small 2nd toe": [ + "HP:0010325" + ], + "absent / underdevelop 2nd toe": [ + "HP:0010325" + ], + "absent / underdeveloped 2nd toe": [ + "HP:0010325" + ], + "deviation of the 2nd toe": [ + "HP:0010326" + ], + "displacement of the 2nd toe": [ + "HP:0010326" + ], + "flexion contracture of the 2nd toe": [ + "HP:0010327" + ], + "joint contracture of the 2nd toe": [ + "HP:0010327" + ], + "joint contractures of the 2nd toe": [ + "HP:0010327" + ], + "polydactyly affect the 2nd toe": [ + "HP:0010328" + ], + "polydactyly affecting the 2nd toe": [ + "HP:0010328" + ], + "abnormality of the epiphysis of the 3rd toe": [ + "HP:0010329" + ], + "abnormality of the epiphyses of the 3rd toe": [ + "HP:0010329" + ], + "abnormality of the end part of the 3rd toe bone": [ + "HP:0010329" + ], + "abnormality of the phalanx of the 3rd toe": [ + "HP:0010330" + ], + "abnormality of the phalanges of the 3rd toe": [ + "HP:0010330" + ], + "abnormality of the bone of the 3rd toe": [ + "HP:0010330" + ], + "abnormality of the bones of the 3rd toe": [ + "HP:0010330" + ], + "aplasia / hypoplasia of the 3rd toe": [ + "HP:0010331" + ], + "absent / hypoplastic third toe": [ + "HP:0010331" + ], + "absent / small 3rd toe": [ + "HP:0010331" + ], + "absent / underdevelop 3rd toe": [ + "HP:0010331" + ], + "absent / underdeveloped 3rd toe": [ + "HP:0010331" + ], + "deviation of the 3rd toe": [ + "HP:0010332" + ], + "displacement of the 3rd toe": [ + "HP:0010332" + ], + "flexion contracture of 3rd toe": [ + "HP:0010333" + ], + "joint contracture of the 3rd toe": [ + "HP:0010333" + ], + "joint contractures of the 3rd toe": [ + "HP:0010333" + ], + "polydactyly affect the 3rd toe": [ + "HP:0010334" + ], + "polydactyly affecting the 3rd toe": [ + "HP:0010334" + ], + "abnormality of the epiphysis of the 4th toe": [ + "HP:0010335" + ], + "abnormality of the epiphyses of the 4th toe": [ + "HP:0010335" + ], + "abnormality of the end part of the 4th toe bone": [ + "HP:0010335" + ], + "abnormality of the phalanx of the 4th toe": [ + "HP:0010336" + ], + "abnormality of the phalanges of the 4th toe": [ + "HP:0010336" + ], + "aplasia / hypoplasia of the 4th toe": [ + "HP:0010337" + ], + "absent / small 4th toe": [ + "HP:0010337" + ], + "absent / underdevelop 4th toe": [ + "HP:0010337" + ], + "absent / underdeveloped 4th toe": [ + "HP:0010337" + ], + "deviation of the 4th toe": [ + "HP:0010338" + ], + "displacement of the 4th toe": [ + "HP:0010338" + ], + "flexion contracture of the 4th toe": [ + "HP:0010339" + ], + "joint contracture of the 4th toe": [ + "HP:0010339" + ], + "joint contractures of the 4th toe": [ + "HP:0010339" + ], + "polydactyly affect the 4th toe": [ + "HP:0010340" + ], + "polydactyly affecting the 4th toe": [ + "HP:0010340" + ], + "abnormality of the epiphysis of the 5th toe": [ + "HP:0010341" + ], + "abnormality of the epiphyses of the 5th toe": [ + "HP:0010341" + ], + "abnormality of the end part of the little toe bone": [ + "HP:0010341" + ], + "abnormality of the end part of the pinkie toe bone": [ + "HP:0010341" + ], + "abnormality of the end part of the pinky toe bone": [ + "HP:0010341" + ], + "abnormality of the phalanx of the 5th toe": [ + "HP:0010342" + ], + "abnormality of the phalanges of the 5th toe": [ + "HP:0010342" + ], + "abnormality of the little toe bone": [ + "HP:0010342" + ], + "abnormality of the little toe bones": [ + "HP:0010342" + ], + "abnormality of the pinkie toe bone": [ + "HP:0010342" + ], + "abnormality of the pinkie toe bones": [ + "HP:0010342" + ], + "abnormality of the pinky toe bone": [ + "HP:0010342" + ], + "abnormality of the pinky toe bones": [ + "HP:0010342" + ], + "aplasia / hypoplasia of the 5th toe": [ + "HP:0010343" + ], + "absent / small little toe": [ + "HP:0010343" + ], + "absent / small pinkie toe": [ + "HP:0010343" + ], + "absent / small pinky toe": [ + "HP:0010343" + ], + "absent / underdevelop pinky toe": [ + "HP:0010343" + ], + "absent / underdeveloped pinky toe": [ + "HP:0010343" + ], + "deviation of the 5th toe": [ + "HP:0010344" + ], + "displacement of the 5th toe": [ + "HP:0010344" + ], + "displacement of the little toe": [ + "HP:0010344" + ], + "displacement of the pinkie toe": [ + "HP:0010344" + ], + "displacement of the pinky toe": [ + "HP:0010344" + ], + "flexion contracture of the 5th toe": [ + "HP:0010345" + ], + "joint contracture of the 5th toe": [ + "HP:0010345" + ], + "joint contractures of the 5th toe": [ + "HP:0010345" + ], + "aplasia / hypoplasia of the phalanx of the 2nd toe": [ + "HP:0010347" + ], + "aplasia / hypoplasia of the phalanges of the 2nd toe": [ + "HP:0010347" + ], + "absent / small bone of 2nd toe": [ + "HP:0010347" + ], + "absent / small bones of 2nd toe": [ + "HP:0010347" + ], + "absent / underdeveloped bone of 2nd toe": [ + "HP:0010347" + ], + "absent / underdeveloped bones of 2nd toe": [ + "HP:0010347" + ], + "broad phalanx of the 2nd toe": [ + "HP:0010348" + ], + "broad phalanges of the 2nd toe": [ + "HP:0010348" + ], + "broad bone of the 2nd toe": [ + "HP:0010348" + ], + "broad bones of the 2nd toe": [ + "HP:0010348" + ], + "bullet - shape 2nd toe phalanx": [ + "HP:0010349" + ], + "bullet - shaped 2nd toe phalanx": [ + "HP:0010349" + ], + "bullet - shaped bone of the 2nd toe": [ + "HP:0010349" + ], + "bullet - shaped bones of the 2nd toe": [ + "HP:0010349" + ], + "bullet - shaped phalanx of the 2nd toe": [ + "HP:0010349" + ], + "bullet - shaped phalanges of the 2nd toe": [ + "HP:0010349" + ], + "curve 2nd toe phalanx": [ + "HP:0010350" + ], + "curved 2nd toe phalanx": [ + "HP:0010350" + ], + "curve bone of the 2nd toe": [ + "HP:0010350" + ], + "curved bones of the 2nd toe": [ + "HP:0010350" + ], + "curve phalanx of the 2nd toe": [ + "HP:0010350" + ], + "curved phalanges of the 2nd toe": [ + "HP:0010350" + ], + "osteolytic defect of the phalanx of the 2nd toe": [ + "HP:0010351" + ], + "osteolytic defects of the phalanges of the 2nd toe": [ + "HP:0010351" + ], + "patchy sclerosis of 2nd toe phalanx": [ + "HP:0010352" + ], + "patchy sclerosis of the phalanx of the 2nd toe": [ + "HP:0010352" + ], + "patchy sclerosis of the phalanges of the 2nd toe": [ + "HP:0010352" + ], + "uneven increase in bone density in 2nd toe bone": [ + "HP:0010352" + ], + "second toe symphalangism": [ + "HP:0010353" + ], + "2nd toe symphalangism": [ + "HP:0010353" + ], + "fuse bone of 2nd toe": [ + "HP:0010353" + ], + "fused bones of 2nd toe": [ + "HP:0010353" + ], + "symphalangism affect the phalanx of the 2nd toe": [ + "HP:0010353" + ], + "symphalangism affecting the phalanges of the 2nd toe": [ + "HP:0010353" + ], + "triangular shape phalanx of the 2nd toe": [ + "HP:0010354" + ], + "triangular shaped phalanges of the 2nd toe": [ + "HP:0010354" + ], + "triangular shape bone of 2nd toe": [ + "HP:0010354" + ], + "triangular shaped bone of 2nd toe": [ + "HP:0010354" + ], + "triangular shape bone of second toe": [ + "HP:0010354" + ], + "triangular shaped bone of second toe": [ + "HP:0010354" + ], + "duplication of the phalanx of the 2nd toe": [ + "HP:0010355" + ], + "duplication of the phalanges of the 2nd toe": [ + "HP:0010355" + ], + "duplication of the bone of the 2nd toe": [ + "HP:0010355" + ], + "duplication of the bones of the 2nd toe": [ + "HP:0010355" + ], + "partial / complete duplication of the phalanx of the 2nd toe": [ + "HP:0010355" + ], + "partial / complete duplication of the phalanges of the 2nd toe": [ + "HP:0010355" + ], + "abnormality of the distal phalanx of the 2nd toe": [ + "HP:0010356" + ], + "abnormality of the outermost bone of the 2nd toe": [ + "HP:0010356" + ], + "abnormality of the middle phalanx of the 2nd toe": [ + "HP:0010357" + ], + "abnormality of the middle bone of the 2nd toe": [ + "HP:0010357" + ], + "abnormal morphology of the proximal phalanx of the 2nd toe": [ + "HP:0010358" + ], + "abnormality of the innermost bone of the 2nd toe": [ + "HP:0010358" + ], + "aplasia / hypoplasia of the phalanx of the 3rd toe": [ + "HP:0010359" + ], + "aplasia / hypoplasia of the phalanges of the 3rd toe": [ + "HP:0010359" + ], + "absent / small bone of 3rd toe": [ + "HP:0010359" + ], + "absent / small bones of 3rd toe": [ + "HP:0010359" + ], + "absent / underdeveloped bone of 3rd toe": [ + "HP:0010359" + ], + "absent / underdeveloped bones of 3rd toe": [ + "HP:0010359" + ], + "broad phalanx of the 3rd toe": [ + "HP:0010360" + ], + "broad phalanges of the 3rd toe": [ + "HP:0010360" + ], + "wide bone of 3rd toe": [ + "HP:0010360" + ], + "wide bones of 3rd toe": [ + "HP:0010360" + ], + "bullet - shape 3rd toe phalanx": [ + "HP:0010361" + ], + "bullet - shaped 3rd toe phalanx": [ + "HP:0010361" + ], + "bullet - shaped bone of 3rd toe": [ + "HP:0010361" + ], + "bullet - shaped bones of 3rd toe": [ + "HP:0010361" + ], + "bullet - shaped phalanx of the 3rd toe": [ + "HP:0010361" + ], + "bullet - shaped phalanges of the 3rd toe": [ + "HP:0010361" + ], + "curve 3rd toe phalanx": [ + "HP:0010362" + ], + "curved 3rd toe phalanx": [ + "HP:0010362" + ], + "curve bone of 3rd toe": [ + "HP:0010362" + ], + "curved bones of 3rd toe": [ + "HP:0010362" + ], + "curve phalanx of the 3rd toe": [ + "HP:0010362" + ], + "curved phalanges of the 3rd toe": [ + "HP:0010362" + ], + "osteolytic defect of the phalanx of the 3rd toe": [ + "HP:0010363" + ], + "osteolytic defects of the phalanges of the 3rd toe": [ + "HP:0010363" + ], + "patchy sclerosis of 3rd toe phalanx": [ + "HP:0010364" + ], + "patchy sclerosis of the phalanx of the 3rd toe": [ + "HP:0010364" + ], + "patchy sclerosis of the phalanges of the 3rd toe": [ + "HP:0010364" + ], + "uneven increase in bone density in 3rd toe bone": [ + "HP:0010364" + ], + "symphalangism affect the phalanx of the 3rd toe": [ + "HP:0010365" + ], + "symphalangism affecting the phalanges of the 3rd toe": [ + "HP:0010365" + ], + "fuse bone of 3rd toe": [ + "HP:0010365" + ], + "fused bones of 3rd toe": [ + "HP:0010365" + ], + "triangular shape phalanx of the 3rd toe": [ + "HP:0010366" + ], + "triangular shaped phalanges of the 3rd toe": [ + "HP:0010366" + ], + "triangular shape 3rd toe bone": [ + "HP:0010366" + ], + "triangular shaped 3rd toe bones": [ + "HP:0010366" + ], + "duplication of phalanx of the 3rd toe": [ + "HP:0010367" + ], + "duplication of 3rd toe bone": [ + "HP:0010367" + ], + "duplication of phalanx of the third toe": [ + "HP:0010367" + ], + "partial / complete duplication of the phalanx of the 3rd toe": [ + "HP:0010367" + ], + "partial / complete duplication of the phalanges of the 3rd toe": [ + "HP:0010367" + ], + "abnormality of the distal phalanx of the 3rd toe": [ + "HP:0010368" + ], + "abnormality of the outermost bone of the 3rd toe": [ + "HP:0010368" + ], + "abnormality of the middle phalanx of the 3rd toe": [ + "HP:0010369" + ], + "abnormality of the middle bone of 3rd toe": [ + "HP:0010369" + ], + "abnormal morphology of the proximal phalanx of the 3rd toe": [ + "HP:0010370" + ], + "abnormality of the innermost bone of 3rd toe": [ + "HP:0010370" + ], + "aplasia / hypoplasia of the phalanx of the 4th toe": [ + "HP:0010371" + ], + "aplasia / hypoplasia of the phalanges of the 4th toe": [ + "HP:0010371" + ], + "absent / small bone of 4th toe": [ + "HP:0010371" + ], + "absent / small bones of 4th toe": [ + "HP:0010371" + ], + "absent / underdeveloped bone of 4th toe": [ + "HP:0010371" + ], + "absent / underdeveloped bones of 4th toe": [ + "HP:0010371" + ], + "broad phalanx of the 4th toe": [ + "HP:0010372" + ], + "broad phalanges of the 4th toe": [ + "HP:0010372" + ], + "broad bone of the 4th toe": [ + "HP:0010372" + ], + "broad bones of the 4th toe": [ + "HP:0010372" + ], + "bullet - shape 4th toe phalanx": [ + "HP:0010373" + ], + "bullet - shaped 4th toe phalanx": [ + "HP:0010373" + ], + "bullet - shaped bone of the 4th toe": [ + "HP:0010373" + ], + "bullet - shaped bones of the 4th toe": [ + "HP:0010373" + ], + "bullet - shaped phalanx of the 4th toe": [ + "HP:0010373" + ], + "bullet - shaped phalanges of the 4th toe": [ + "HP:0010373" + ], + "curve 4th toe phalanx": [ + "HP:0010374" + ], + "curved 4th toe phalanx": [ + "HP:0010374" + ], + "curve bone of 4th toe": [ + "HP:0010374" + ], + "curved bones of 4th toe": [ + "HP:0010374" + ], + "curve phalanx of the 4th toe": [ + "HP:0010374" + ], + "curved phalanges of the 4th toe": [ + "HP:0010374" + ], + "osteolytic defect of the phalanx of the 4th toe": [ + "HP:0010375" + ], + "osteolytic defects of the phalanges of the 4th toe": [ + "HP:0010375" + ], + "patchy sclerosis of 4th toe phalanx": [ + "HP:0010376" + ], + "patchy sclerosis of the phalanx of the 4th toe": [ + "HP:0010376" + ], + "patchy sclerosis of the phalanges of the 4th toe": [ + "HP:0010376" + ], + "uneven increase in bone density in 4th toe bone": [ + "HP:0010376" + ], + "symphalangism affect the phalanx of the 4th toe": [ + "HP:0010377" + ], + "symphalangism affecting the phalanges of the 4th toe": [ + "HP:0010377" + ], + "fuse bone of 4th toe": [ + "HP:0010377" + ], + "fused bones of 4th toe": [ + "HP:0010377" + ], + "triangular shape phalanx of the 4th toe": [ + "HP:0010378" + ], + "triangular shaped phalanges of the 4th toe": [ + "HP:0010378" + ], + "triangular shape bone of 4th toe": [ + "HP:0010378" + ], + "triangular shaped bones of 4th toe": [ + "HP:0010378" + ], + "duplication of phalanx of the 4th toe": [ + "HP:0010379" + ], + "duplication of 4th toe bone": [ + "HP:0010379" + ], + "duplication of phalanx of the fourth toe": [ + "HP:0010379" + ], + "partial / complete duplication of the phalanx of the 4th toe": [ + "HP:0010379" + ], + "partial / complete duplication of the phalanges of the 4th toe": [ + "HP:0010379" + ], + "abnormality of the distal phalanx of the 4th toe": [ + "HP:0010380" + ], + "abnormality of the outermost 4th toe bone": [ + "HP:0010380" + ], + "abnormality of the middle phalanx of the 4th toe": [ + "HP:0010381" + ], + "abnormality of middle 4th toe bone": [ + "HP:0010381" + ], + "abnormal morphology of the proximal phalanx of the 4th toe": [ + "HP:0010382" + ], + "abnormal innermost 4th toe bone": [ + "HP:0010382" + ], + "aplasia / hypoplasia of the phalanx of the 5th toe": [ + "HP:0010383" + ], + "aplasia / hypoplasia of the phalanges of the 5th toe": [ + "HP:0010383" + ], + "absent / small little toe bone": [ + "HP:0010383" + ], + "absent / small little toe bones": [ + "HP:0010383" + ], + "absent / small pinkie toe bone": [ + "HP:0010383" + ], + "absent / small pinkie toe bones": [ + "HP:0010383" + ], + "absent / small pinky toe bone": [ + "HP:0010383" + ], + "absent / small pinky toe bones": [ + "HP:0010383" + ], + "absent / underdevelop pinky toe bone": [ + "HP:0010383" + ], + "absent / underdeveloped pinky toe bones": [ + "HP:0010383" + ], + "broad phalanx of the 5th toe": [ + "HP:0010384" + ], + "broad phalanges of the 5th toe": [ + "HP:0010384" + ], + "broad bone of the little toe": [ + "HP:0010384" + ], + "broad bones of the little toe": [ + "HP:0010384" + ], + "broad bone of the pinkie toe": [ + "HP:0010384" + ], + "broad bones of the pinkie toe": [ + "HP:0010384" + ], + "broad bone of the pinky toe": [ + "HP:0010384" + ], + "broad bones of the pinky toe": [ + "HP:0010384" + ], + "bullet - shape 5th toe phalanx": [ + "HP:0010385" + ], + "bullet - shaped 5th toe phalanx": [ + "HP:0010385" + ], + "bullet - shaped bone of the little toe": [ + "HP:0010385" + ], + "bullet - shaped bones of the little toe": [ + "HP:0010385" + ], + "bullet - shaped bone of the pinkie toe": [ + "HP:0010385" + ], + "bullet - shaped bones of the pinkie toe": [ + "HP:0010385" + ], + "bullet - shaped bone of the pinky toe": [ + "HP:0010385" + ], + "bullet - shaped bones of the pinky toe": [ + "HP:0010385" + ], + "bullet - shaped phalanx of the 5th toe": [ + "HP:0010385" + ], + "bullet - shaped phalanges of the 5th toe": [ + "HP:0010385" + ], + "curve 5th toe phalanx": [ + "HP:0010386" + ], + "curved 5th toe phalanx": [ + "HP:0010386" + ], + "curve little toe bone": [ + "HP:0010386" + ], + "curved little toe bones": [ + "HP:0010386" + ], + "curve phalanx of the 5th toe": [ + "HP:0010386" + ], + "curved phalanges of the 5th toe": [ + "HP:0010386" + ], + "curve pinkie toe bone": [ + "HP:0010386" + ], + "curved pinkie toe bones": [ + "HP:0010386" + ], + "curve pinky toe bone": [ + "HP:0010386" + ], + "curved pinky toe bones": [ + "HP:0010386" + ], + "osteolytic defect of the phalanx of the 5th toe": [ + "HP:0010387" + ], + "osteolytic defects of the phalanges of the 5th toe": [ + "HP:0010387" + ], + "patchy sclerosis of 5th toe phalanx": [ + "HP:0010388" + ], + "patchy sclerosis of the phalanx of the 5th toe": [ + "HP:0010388" + ], + "patchy sclerosis of the phalanges of the 5th toe": [ + "HP:0010388" + ], + "uneven increase in bone density in little toe bone": [ + "HP:0010388" + ], + "uneven increase in bone density in pinkie toe bone": [ + "HP:0010388" + ], + "uneven increase in bone density in pinky toe bone": [ + "HP:0010388" + ], + "symphalangism affect the phalanx of the 5th toe": [ + "HP:0010389" + ], + "symphalangism affecting the phalanges of the 5th toe": [ + "HP:0010389" + ], + "fuse bone in the little toe": [ + "HP:0010389" + ], + "fused bones in the little toe": [ + "HP:0010389" + ], + "fuse bone in the pinkie toe": [ + "HP:0010389" + ], + "fused bones in the pinkie toe": [ + "HP:0010389" + ], + "fuse bone in the pinky toe": [ + "HP:0010389" + ], + "fused bones in the pinky toe": [ + "HP:0010389" + ], + "triangular shape phalanx of the 5th toe": [ + "HP:0010390" + ], + "triangular shaped phalanges of the 5th toe": [ + "HP:0010390" + ], + "triangular shape little toe bone": [ + "HP:0010390" + ], + "triangular shaped little toe bone": [ + "HP:0010390" + ], + "triangular shape pinkie toe bone": [ + "HP:0010390" + ], + "triangular shaped pinkie toe bone": [ + "HP:0010390" + ], + "triangular shape pinky toe bone": [ + "HP:0010390" + ], + "triangular shaped pinky toe bone": [ + "HP:0010390" + ], + "duplication of the phalanx of the 5th toe": [ + "HP:0010391" + ], + "duplication of the phalanges of the 5th toe": [ + "HP:0010391" + ], + "duplication of the bone of the little toe": [ + "HP:0010391" + ], + "duplication of the bones of the little toe": [ + "HP:0010391" + ], + "duplication of the bone of the pinkie toe": [ + "HP:0010391" + ], + "duplication of the bones of the pinkie toe": [ + "HP:0010391" + ], + "duplication of the bone of the pinky toe": [ + "HP:0010391" + ], + "duplication of the bones of the pinky toe": [ + "HP:0010391" + ], + "duplication of the phalanx of the fifth toe": [ + "HP:0010391" + ], + "duplication of the phalanges of the fifth toe": [ + "HP:0010391" + ], + "partial / complete duplication of the phalanx of the 5th toe": [ + "HP:0010391" + ], + "partial / complete duplication of the phalanges of the 5th toe": [ + "HP:0010391" + ], + "abnormality of the distal phalanx of the 5th toe": [ + "HP:0010392" + ], + "abnormality of the outermost bone of the little toe": [ + "HP:0010392" + ], + "abnormality of the outermost bone of the pinkie toe": [ + "HP:0010392" + ], + "abnormality of the outermost bone of the pinky toe": [ + "HP:0010392" + ], + "abnormality of the middle phalanx of the 5th toe": [ + "HP:0010393" + ], + "abnormality of the middle bone of the little toe": [ + "HP:0010393" + ], + "abnormality of the middle bone of the pinkie toe": [ + "HP:0010393" + ], + "abnormality of the middle bone of the pinky toe": [ + "HP:0010393" + ], + "abnormal morphology of the proximal phalanx of the 5th toe": [ + "HP:0010394" + ], + "abnormality of the innermost bone of the little toe": [ + "HP:0010394" + ], + "abnormality of the innermost bone of the pinkie toe": [ + "HP:0010394" + ], + "abnormality of the innermost bone of the pinky toe": [ + "HP:0010394" + ], + "aplasia / hypoplasia of the proximal phalanx of the 2nd toe": [ + "HP:0010395" + ], + "absent / small innermost 2nd toe bone": [ + "HP:0010395" + ], + "absent / underdevelop innermost 2nd toe bone": [ + "HP:0010395" + ], + "absent / underdeveloped innermost 2nd toe bone": [ + "HP:0010395" + ], + "broad proximal phalanx of the 2nd toe": [ + "HP:0010396" + ], + "broad innermost bone of 2nd toe": [ + "HP:0010396" + ], + "bullet - shape proximal phalanx of the 2nd toe": [ + "HP:0010397" + ], + "bullet - shaped proximal phalanx of the 2nd toe": [ + "HP:0010397" + ], + "bullet - shape innermost bone of 2nd toe": [ + "HP:0010397" + ], + "bullet - shaped innermost bone of 2nd toe": [ + "HP:0010397" + ], + "curve proximal phalanx of the 2nd toe": [ + "HP:0010398" + ], + "curved proximal phalanx of the 2nd toe": [ + "HP:0010398" + ], + "curve innermost bone of 2nd toe": [ + "HP:0010398" + ], + "curved innermost bone of 2nd toe": [ + "HP:0010398" + ], + "osteolytic defect of the proximal phalanx of the 2nd toe": [ + "HP:0010399" + ], + "osteolytic defects of the proximal phalanx of the 2nd toe": [ + "HP:0010399" + ], + "patchy sclerosis of the proximal phalanx of the 2nd toe": [ + "HP:0010400" + ], + "uneven increase in bone density in the innermost bone of the 2nd toe": [ + "HP:0010400" + ], + "symphalangism affect the proximal phalanx of the 2nd toe": [ + "HP:0010401" + ], + "symphalangism affecting the proximal phalanx of the 2nd toe": [ + "HP:0010401" + ], + "fuse innermost bone of the 2nd toe": [ + "HP:0010401" + ], + "fused innermost bone of the 2nd toe": [ + "HP:0010401" + ], + "triangular shape proximal phalanx of the 2nd toe": [ + "HP:0010402" + ], + "triangular shaped proximal phalanx of the 2nd toe": [ + "HP:0010402" + ], + "triangular shape innermost 2nd toe bone": [ + "HP:0010402" + ], + "triangular shaped innermost 2nd toe bone": [ + "HP:0010402" + ], + "duplication of the proximal phalanx of the 2nd toe": [ + "HP:0010403" + ], + "duplication of innermost 2nd toe bone": [ + "HP:0010403" + ], + "duplication of the proximal phalanx of the second toe": [ + "HP:0010403" + ], + "partial / complete duplication of the proximal phalanx of the 2nd toe": [ + "HP:0010403" + ], + "aplasia / hypoplasia of the middle phalanx of the 2nd toe": [ + "HP:0010404" + ], + "absent / small middle bone of 2nd toe": [ + "HP:0010404" + ], + "absent / underdevelop middle bone of 2nd toe": [ + "HP:0010404" + ], + "absent / underdeveloped middle bone of 2nd toe": [ + "HP:0010404" + ], + "broad middle phalanx of the 2nd toe": [ + "HP:0010405" + ], + "broad middle bone of 2nd toe": [ + "HP:0010405" + ], + "bullet - shape middle phalanx of the 2nd toe": [ + "HP:0010406" + ], + "bullet - shaped middle phalanx of the 2nd toe": [ + "HP:0010406" + ], + "bullet - shape middle bone of 2nd toe": [ + "HP:0010406" + ], + "bullet - shaped middle bone of 2nd toe": [ + "HP:0010406" + ], + "curve middle phalanx of the 2nd toe": [ + "HP:0010407" + ], + "curved middle phalanx of the 2nd toe": [ + "HP:0010407" + ], + "curve middle bone of 2nd toe": [ + "HP:0010407" + ], + "curved middle bone of 2nd toe": [ + "HP:0010407" + ], + "osteolytic defect of the middle phalanx of the 2nd toe": [ + "HP:0010408" + ], + "osteolytic defects of the middle phalanx of the 2nd toe": [ + "HP:0010408" + ], + "patchy sclerosis of the middle phalanx of the 2nd toe": [ + "HP:0010409" + ], + "uneven increase in bone density in the middle bone of the 2nd toe": [ + "HP:0010409" + ], + "symphalangism affect the middle phalanx of the 2nd toe": [ + "HP:0010410" + ], + "symphalangism affecting the middle phalanx of the 2nd toe": [ + "HP:0010410" + ], + "fuse middle bone of 2nd toe": [ + "HP:0010410" + ], + "fused middle bone of 2nd toe": [ + "HP:0010410" + ], + "triangular shape middle phalanx of the 2nd toe": [ + "HP:0010411" + ], + "triangular shaped middle phalanx of the 2nd toe": [ + "HP:0010411" + ], + "triangular shape middle bone of 2nd toe": [ + "HP:0010411" + ], + "triangular shaped middle bone of 2nd toe": [ + "HP:0010411" + ], + "duplication of the middle phalanx of the 2nd toe": [ + "HP:0010412" + ], + "duplication of middle bone of 2nd toe": [ + "HP:0010412" + ], + "partial / complete duplication of the middle phalanx of the 2nd toe": [ + "HP:0010412" + ], + "aplasia / hypoplasia of the distal phalanx of the 2nd toe": [ + "HP:0010413" + ], + "absent / small outermost 2nd toe bone": [ + "HP:0010413" + ], + "absent / underdevelop outermost 2nd toe bone": [ + "HP:0010413" + ], + "absent / underdeveloped outermost 2nd toe bone": [ + "HP:0010413" + ], + "broad distal phalanx of the 2nd toe": [ + "HP:0010414" + ], + "broad outermost bone of the 2nd toe": [ + "HP:0010414" + ], + "wide outermost bone of the 2nd toe": [ + "HP:0010414" + ], + "bullet - shaped distal phalanx of the 2nd toe": [ + "HP:0010415" + ], + "bullet - shape outermost bone of the 2nd toe": [ + "HP:0010415" + ], + "bullet - shaped outermost bone of the 2nd toe": [ + "HP:0010415" + ], + "curve distal phalanx of the 2nd toe": [ + "HP:0010416" + ], + "curved distal phalanx of the 2nd toe": [ + "HP:0010416" + ], + "curve outermost bone of the 2nd toe": [ + "HP:0010416" + ], + "curved outermost bone of the 2nd toe": [ + "HP:0010416" + ], + "osteolytic defect of the distal phalanx of the 2nd toe": [ + "HP:0010417" + ], + "osteolytic defects of the distal phalanx of the 2nd toe": [ + "HP:0010417" + ], + "patchy sclerosis of the distal phalanx of the 2nd toe": [ + "HP:0010418" + ], + "uneven increase in bone density in the outermost bone of the 2nd toe": [ + "HP:0010418" + ], + "symphalangism affect the distal phalanx of the 2nd toe": [ + "HP:0010419" + ], + "symphalangism affecting the distal phalanx of the 2nd toe": [ + "HP:0010419" + ], + "fuse outermost bone of the 2nd toe": [ + "HP:0010419" + ], + "fused outermost bone of the 2nd toe": [ + "HP:0010419" + ], + "triangular shape distal phalanx of the 2nd toe": [ + "HP:0010420" + ], + "triangular shaped distal phalanx of the 2nd toe": [ + "HP:0010420" + ], + "triangular shape outermost 2nd toe bone": [ + "HP:0010420" + ], + "triangular shaped outermost 2nd toe bone": [ + "HP:0010420" + ], + "duplication of the distal phalanx of the 2nd toe": [ + "HP:0010421" + ], + "duplication of the outermost bone of the 2nd toe": [ + "HP:0010421" + ], + "partial / complete duplication of the distal phalanx of the 2nd toe": [ + "HP:0010421" + ], + "complete duplication of the proximal phalanx of the 2nd toe": [ + "HP:0010422" + ], + "complete duplication of the innermost 2nd toe bone": [ + "HP:0010422" + ], + "complete duplication of the proximal phalanx of the second toe": [ + "HP:0010422" + ], + "partial duplication of the proximal phalanx of the 2nd toe": [ + "HP:0010423" + ], + "partial duplication of the innermost 2nd toe bone": [ + "HP:0010423" + ], + "partial duplication of the proximal phalanx of the second toe": [ + "HP:0010423" + ], + "complete duplication of the distal phalanx of the 2nd toe": [ + "HP:0010424" + ], + "complete duplication of the outermost bone of the 2nd toe": [ + "HP:0010424" + ], + "partial duplication of the distal phalanx of the 2nd toe": [ + "HP:0010425" + ], + "partial duplication of the outermost bone of the 2nd toe": [ + "HP:0010425" + ], + "complete duplication of the middle phalanx of the 2nd toe": [ + "HP:0010426" + ], + "complete duplication of the middle bone of the 2nd toe": [ + "HP:0010426" + ], + "partial duplication of the middle phalanx of the 2nd toe": [ + "HP:0010427" + ], + "partial duplication of the middle bone of the 2nd toe": [ + "HP:0010427" + ], + "partial duplication of phalanx of the 2nd toe": [ + "HP:0010428" + ], + "partial duplication of 2nd toe bone": [ + "HP:0010428" + ], + "complete duplication of the phalanx of the 2nd toe": [ + "HP:0010429" + ], + "complete duplication of the phalanges of the 2nd toe": [ + "HP:0010429" + ], + "complete duplication of the 2nd toe bone": [ + "HP:0010429" + ], + "complete duplication of the 2nd toe bones": [ + "HP:0010429" + ], + "aplasia of the phalanx of the 2nd toe": [ + "HP:0010430" + ], + "aplasia of the phalanges of the 2nd toe": [ + "HP:0010430" + ], + "absent 2nd toe bone": [ + "HP:0010430" + ], + "absent 2nd toe bones": [ + "HP:0010430" + ], + "short phalanx of the 2nd toe": [ + "HP:0010431" + ], + "hypoplastic / small phalanx of the 2nd toe": [ + "HP:0010431" + ], + "hypoplastic / small phalanges of the 2nd toe": [ + "HP:0010431" + ], + "short 2nd toe bone": [ + "HP:0010431" + ], + "short phalanx of the second toe": [ + "HP:0010431" + ], + "absent distal phalanx of the 2nd toe": [ + "HP:0010432" + ], + "absent distal phalanx of the second toe": [ + "HP:0010432" + ], + "absent outermost bone of the 2nd toe": [ + "HP:0010432" + ], + "aplasia of the distal phalanx of the 2nd toe": [ + "HP:0010432" + ], + "short distal phalanx of the 2nd toe": [ + "HP:0010433" + ], + "hypoplastic / small distal phalanx of the 2nd toe": [ + "HP:0010433" + ], + "short distal phalanx of the second toe": [ + "HP:0010433" + ], + "short outermost bone of the 2nd toe": [ + "HP:0010433" + ], + "aplasia of the middle phalanx of the 2nd toe": [ + "HP:0010434" + ], + "absent middle bone of 2nd toe": [ + "HP:0010434" + ], + "short middle phalanx of the 2nd toe": [ + "HP:0010435" + ], + "hypoplastic / small middle phalanx of the 2nd toe": [ + "HP:0010435" + ], + "short middle 2nd toe bone": [ + "HP:0010435" + ], + "short middle phalanx of the second toe": [ + "HP:0010435" + ], + "aplasia of the proximal phalanx of the 2nd toe": [ + "HP:0010436" + ], + "absent innermost 2nd toe bone": [ + "HP:0010436" + ], + "short proximal phalanx of the 2nd toe": [ + "HP:0010437" + ], + "hypoplastic / small proximal phalanx of the 2nd toe": [ + "HP:0010437" + ], + "short innermost 2nd toe bone": [ + "HP:0010437" + ], + "short proximal phalanx of the second toe": [ + "HP:0010437" + ], + "abnormal ventricular septum morphology": [ + "HP:0010438" + ], + "abnormal interventricular septum morphology": [ + "HP:0010438" + ], + "abnormality of the ventricular septum": [ + "HP:0010438" + ], + "ventricular septum abnormality": [ + "HP:0010438" + ], + "ectopic accesory toe - like appendage": [ + "HP:0010440" + ], + "ectopic accessory finger - like appendage": [ + "HP:0010441" + ], + "polydactyly": [ + "HP:0010442" + ], + "more than five finger or toe on hand or foot": [ + "HP:0010442" + ], + "more than five fingers or toes on hands or feet": [ + "HP:0010442" + ], + "bifid femur": [ + "HP:0010443" + ], + "notch thighbone": [ + "HP:0010443" + ], + "notched thighbone": [ + "HP:0010443" + ], + "split thighbone": [ + "HP:0010443" + ], + "pulmonary insufficiency": [ + "HP:0010444" + ], + "pulmonary incompetence": [ + "HP:0010444" + ], + "puolmonary valve insufficiency": [ + "HP:0010444" + ], + "primum atrial septal defect": [ + "HP:0010445" + ], + "atrial septal defect , primum type": [ + "HP:0010445" + ], + "ostium primum atrial septal defect": [ + "HP:0010445" + ], + "primum atrioventricular canal defect": [ + "HP:0010445" + ], + "septum primum defect": [ + "HP:0010445" + ], + "tricuspid stenosis": [ + "HP:0010446" + ], + "anal fistula": [ + "HP:0010447" + ], + "fistula in ano": [ + "HP:0010447" + ], + "colonic atresia": [ + "HP:0010448" + ], + "atresia of the large intestine": [ + "HP:0010448" + ], + "large intestinal atresia": [ + "HP:0010448" + ], + "esophageal stenosis": [ + "HP:0010450" + ], + "narrowing of the esophagus": [ + "HP:0010450" + ], + "narrowing of the oesophagus": [ + "HP:0010450" + ], + "aplasia / hypoplasia of the spleen": [ + "HP:0010451" + ], + "absent / small spleen": [ + "HP:0010451" + ], + "absent / underdevelop spleen": [ + "HP:0010451" + ], + "absent / underdeveloped spleen": [ + "HP:0010451" + ], + "ectopia of the spleen": [ + "HP:0010452" + ], + "abnormal spleen location": [ + "HP:0010452" + ], + "ectopic spleen": [ + "HP:0010452" + ], + "pelvic bone asymmetry": [ + "HP:0010453" + ], + "asymmetric pelvis": [ + "HP:0010453" + ], + "pelvic asymmetry": [ + "HP:0010453" + ], + "acetabular spur": [ + "HP:0010454" + ], + "acetabular spurs": [ + "HP:0010454" + ], + "steep acetabular roof": [ + "HP:0010455" + ], + "abnormal great sciatic notch morphology": [ + "HP:0010456" + ], + "abnormal greater sciatic notch morphology": [ + "HP:0010456" + ], + "abnormality of great sciatic notch": [ + "HP:0010456" + ], + "abnormality of greater sciatic notch": [ + "HP:0010456" + ], + "abnormality of the great sacrosciatic notch": [ + "HP:0010456" + ], + "abnormality of the greater sacrosciatic notch": [ + "HP:0010456" + ], + "abnormality of the sacroiliac notch": [ + "HP:0010456" + ], + "obsolete widening of the sacrosciatic notch": [ + "HP:0010457" + ], + "female pseudohermaphroditism": [ + "HP:0010458" + ], + "true hermaphroditism": [ + "HP:0010459" + ], + "testicular and ovarian tissue present": [ + "HP:0010459" + ], + "abnormality of the female genitalia": [ + "HP:0010460" + ], + "abnormality of the male genitalia": [ + "HP:0010461" + ], + "abnormal male genitals": [ + "HP:0010461" + ], + "aplasia / hypoplasia of the ovary": [ + "HP:0010462" + ], + "absent / small ovary": [ + "HP:0010462" + ], + "absent / underdevelop ovary": [ + "HP:0010462" + ], + "absent / underdeveloped ovary": [ + "HP:0010462" + ], + "aplasia of the ovary": [ + "HP:0010463" + ], + "absent ovary": [ + "HP:0010463" + ], + "aplasia of the ovaries": [ + "HP:0010463" + ], + "bilateral absent ovary": [ + "HP:0010463" + ], + "bilateral absent ovaries": [ + "HP:0010463" + ], + "streak ovary": [ + "HP:0010464" + ], + "precocious puberty in female": [ + "HP:0010465" + ], + "precocious puberty in females": [ + "HP:0010465" + ], + "aplasia / hypoplasia of the testis": [ + "HP:0010468" + ], + "aplasia / hypoplasia of the testes": [ + "HP:0010468" + ], + "absent / small testis": [ + "HP:0010468" + ], + "absent / small testes": [ + "HP:0010468" + ], + "absent / underdevelop testis": [ + "HP:0010468" + ], + "absent / underdeveloped testes": [ + "HP:0010468" + ], + "absent testis": [ + "HP:0010469" + ], + "absence of palpable testicules": [ + "HP:0010469" + ], + "absent testes": [ + "HP:0010469" + ], + "aplasia of the testis": [ + "HP:0010469" + ], + "aplasia of the testes": [ + "HP:0010469" + ], + "supernumerary testis": [ + "HP:0010470" + ], + "supernumerary testes": [ + "HP:0010470" + ], + "extra testis": [ + "HP:0010470" + ], + "extra testes": [ + "HP:0010470" + ], + "polyorchidism": [ + "HP:0010470" + ], + "oligosacchariduria": [ + "HP:0010471" + ], + "abnormal circulate porphyrin concentration": [ + "HP:0010472" + ], + "abnormal circulating porphyrin concentration": [ + "HP:0010472" + ], + "porphyrinuria": [ + "HP:0010473" + ], + "bladder stone": [ + "HP:0010474" + ], + "bladder stones": [ + "HP:0010474" + ], + "cloacal exstrophy": [ + "HP:0010475" + ], + "aplasia / hypoplasia of the bladder": [ + "HP:0010476" + ], + "absent / small bladder": [ + "HP:0010476" + ], + "absent / underdevelop bladder": [ + "HP:0010476" + ], + "absent / underdeveloped bladder": [ + "HP:0010476" + ], + "aplasia of the bladder": [ + "HP:0010477" + ], + "absent bladder": [ + "HP:0010477" + ], + "abnormality of the urachus": [ + "HP:0010478" + ], + "patent urachus": [ + "HP:0010479" + ], + "persistent urachus": [ + "HP:0010479" + ], + "urethral fistula": [ + "HP:0010480" + ], + "urethral valve": [ + "HP:0010481" + ], + "acromelia of the upper limb": [ + "HP:0010482" + ], + "acromelia of the upper limbs": [ + "HP:0010482" + ], + "amniotic constriction ring of arm": [ + "HP:0010483" + ], + "amniotic constriction rings of arms": [ + "HP:0010483" + ], + "hypertrophy of the upper limb": [ + "HP:0010484" + ], + "increase size of upper limb": [ + "HP:0010484" + ], + "increased size of upper limb": [ + "HP:0010484" + ], + "hyperextensibility at elbow": [ + "HP:0010485" + ], + "abnormality of the hypothenar eminence": [ + "HP:0010486" + ], + "small hypothenar eminence": [ + "HP:0010487" + ], + "hypoplasia of the hypothenar eminence": [ + "HP:0010487" + ], + "hypothenar hypoplasia": [ + "HP:0010487" + ], + "aplasia / hypoplasia of the palmar crease": [ + "HP:0010488" + ], + "aplasia / hypoplasia of the palmar creases": [ + "HP:0010488" + ], + "absent / small palm crease": [ + "HP:0010488" + ], + "absent / underdevelop palm crease": [ + "HP:0010488" + ], + "absent / underdeveloped palm crease": [ + "HP:0010488" + ], + "absent palmar crease": [ + "HP:0010489" + ], + "absence of the palmar crease": [ + "HP:0010489" + ], + "absence of the palmar creases": [ + "HP:0010489" + ], + "absent palm line": [ + "HP:0010489" + ], + "absent palm lines": [ + "HP:0010489" + ], + "aplasia of the palmar crease": [ + "HP:0010489" + ], + "aplasia of the palmar creases": [ + "HP:0010489" + ], + "abnormality of the palmar crease": [ + "HP:0010490" + ], + "abnormality of the palmar creases": [ + "HP:0010490" + ], + "abnormality of the palm line": [ + "HP:0010490" + ], + "abnormality of the palm lines": [ + "HP:0010490" + ], + "digital constriction ring": [ + "HP:0010491" + ], + "amniotic constriction ring of digit": [ + "HP:0010491" + ], + "amniotic constriction rings of digits": [ + "HP:0010491" + ], + "osseous finger syndactyly": [ + "HP:0010492" + ], + "osseous syndactyly of the finger": [ + "HP:0010492" + ], + "osseous syndactyly of the fingers": [ + "HP:0010492" 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"limitation of knee mobility": [ + "HP:0010501" + ], + "limited knee movement": [ + "HP:0010501" + ], + "fibular bowing": [ + "HP:0010502" + ], + "bow calf bone": [ + "HP:0010502" + ], + "bowed calf bone": [ + "HP:0010502" + ], + "fibular duplication": [ + "HP:0010503" + ], + "duplicate calf bone": [ + "HP:0010503" + ], + "duplicated calf bone": [ + "HP:0010503" + ], + "increased length of the tibia": [ + "HP:0010504" + ], + "increased length of shankbone": [ + "HP:0010504" + ], + "increased length of shinbone": [ + "HP:0010504" + ], + "limitation of movement at ankle": [ + "HP:0010505" + ], + "limitation of movement at ankles": [ + "HP:0010505" + ], + "abnormal plantar dermatoglyphic": [ + "HP:0010506" + ], + "abnormal plantar dermatoglyphics": [ + "HP:0010506" + ], + "abnormal dermatoglyphic on foot": [ + "HP:0010506" + ], + "abnormal dermatoglyphics on feet": [ + "HP:0010506" + ], + "abnormal print on foot": [ + "HP:0010506" + ], + "abnormal prints on feet": [ + "HP:0010506" + ], + "foot asymmetry": [ + "HP:0010507" + ], + "metatarsus valgus": [ + "HP:0010508" + ], + "aplasia of the tarsal bone": [ + "HP:0010509" + ], + "aplasia of the tarsal bones": [ + "HP:0010509" + ], + "absent ankle bone": [ + "HP:0010509" + ], + "absent tarsal": [ + "HP:0010509" + ], + "absent tarsals": [ + "HP:0010509" + ], + "hypermobility of toe joint": [ + "HP:0010510" + ], + "hypermobility of toe joints": [ + "HP:0010510" + ], + "long toe": [ + "HP:0010511" + ], + "increased length of toe": [ + "HP:0010511" + ], + "increased length of toes": [ + "HP:0010511" + ], + "long toes": [ + "HP:0010511" + ], + "adrenal calcification": [ + "HP:0010512" + ], + "pituitary calcification": [ + "HP:0010513" + ], + "hyperpituitarism": [ + "HP:0010514" + ], + "aplasia / hypoplasia of the thymus": [ + "HP:0010515" + ], + "absent / small thymus": [ + "HP:0010515" + ], + "absent / underdevelop thymus": [ + "HP:0010515" + ], + "absent / underdeveloped thymus": [ + "HP:0010515" + ], + "thymic hypoplasia or aplasia": [ + "HP:0010515" + ], + "thymus hyperplasia": [ + "HP:0010516" + ], + "enlarge thymus": [ + "HP:0010516" + ], + "enlarged thymus": [ + "HP:0010516" + ], + "thymic hyperplasia": [ + "HP:0010516" + ], + "ectopic thymus tissue": [ + "HP:0010517" + ], + "abnormal thymus position": [ + "HP:0010517" + ], + "thyroglossal cyst": [ + "HP:0010518" + ], + "thyroglossal duct cyst": [ + "HP:0010518" + ], + "increase fetal movement": [ + "HP:0010519" + ], + "increased fetal movement": [ + "HP:0010519" + ], + "fetal hyperkinesia": [ + "HP:0010519" + ], + "foetal hyperkinesia": [ + "HP:0010519" + ], + "increase foetal movement": [ + "HP:0010519" + ], + "increased foetal movement": [ + "HP:0010519" + ], + "gait apraxia": [ + "HP:0010521" + ], + "dyslexia": [ + "HP:0010522" + ], + "reading disability": [ + "HP:0010522" + ], + "alexia": [ + "HP:0010523" + ], + "text blindness": [ + "HP:0010523" + ], + "word blindness": [ + "HP:0010523" + ], + "agnosia": [ + "HP:0010524" + ], + "finger agnosia": [ + "HP:0010525" + ], + "dysgraphia": [ + "HP:0010526" + ], + "astereognosia": [ + "HP:0010527" + ], + "astereognosis": [ + "HP:0010527" + ], + "somatosensory agnosia": [ + "HP:0010527" + ], + "prosopagnosia": [ + "HP:0010528" + ], + "face blindness": [ + "HP:0010528" + ], + "facial agnosia": [ + "HP:0010528" + ], + "echolalia": [ + "HP:0010529" + ], + "echo another person 's speech": [ + "HP:0010529" + ], + "echoing another person 's speech": [ + "HP:0010529" + ], + "echologia": [ + "HP:0010529" + ], + "echophrasia": [ + "HP:0010529" + ], + "repeat speech": [ + "HP:0010529" + ], + "repeated speech": [ + "HP:0010529" + ], + "palatal myoclonus": [ + "HP:0010530" + ], + "spinal myoclonus": [ + "HP:0010531" + ], + "paroxysmal vertigo": [ + "HP:0010532" + ], + "spasmus nutans": [ + "HP:0010533" + ], + "transient global amnesia": [ + "HP:0010534" + ], + "sleep apnea": [ + "HP:0010535" + ], + "pause in breathe while sleep": [ + "HP:0010535" + ], + "pauses in breathing while sleeping": [ + "HP:0010535" + ], + "sleep apnoea": [ + "HP:0010535" + ], + "central sleep apnea": [ + "HP:0010536" + ], + "central sleep apnoea": [ + "HP:0010536" + ], + "wide cranial suture": [ + "HP:0010537" + ], + "wide cranial sutures": [ + "HP:0010537" + ], + "broad cranial suture": [ + "HP:0010537" + ], + "broad cranial sutures": [ + "HP:0010537" + ], + "large cranial suture": [ + "HP:0010537" + ], + "open cranial suture": [ + "HP:0010537" + ], + "open cranial sutures": [ + "HP:0010537" + ], + "persistent open cranial suture": [ + "HP:0010537" + ], + "persistent open cranial sutures": [ + "HP:0010537" + ], + "widen cranial suture": [ + "HP:0010537" + ], + "widened cranial sutures": [ + "HP:0010537" + ], + "small sella turcica": [ + "HP:0010538" + ], + "hypoplasia of hypophseal fossa": [ + "HP:0010538" + ], + "hypoplasia of pituitary fossa": [ + "HP:0010538" + ], + "hypoplasia of sella turcica": [ + "HP:0010538" + ], + "small hypophyseal fossa": [ + "HP:0010538" + ], + "small pituitary fossa": [ 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nystagmus": [ + "HP:0010545" + ], + "muscle fibrillation": [ + "HP:0010546" + ], + "twitch": [ + "HP:0010546" + ], + "twitching": [ + "HP:0010546" + ], + "muscle flaccidity": [ + "HP:0010547" + ], + "percussion myotonia": [ + "HP:0010548" + ], + "transient swelling of muscle induce by percussion": [ + "HP:0010548" + ], + "transient swelling of muscle induced by percussion": [ + "HP:0010548" + ], + "weakness due to upper motor neuron dysfunction": [ + "HP:0010549" + ], + "paralysis due to lesion of the principle motor tract": [ + "HP:0010549" + ], + "paralysis due to lesions of the principle motor tracts": [ + "HP:0010549" + ], + "paraplegia": [ + "HP:0010550" + ], + "leg paralysis": [ + "HP:0010550" + ], + "paraplegia / paraparesis": [ + "HP:0010551" + ], + "oculogyric crisis": [ + "HP:0010553" + ], + "cutaneous finger syndactyly": [ + "HP:0010554" + ], + "cutaneous syndactyly of finger": [ + "HP:0010554" + ], + "cutaneous syndactyly of fingers": [ + "HP:0010554" + ], + "cutaneous syndactyly of hand": [ + "HP:0010554" + ], + "cutaneous syndactyly of hands": [ + "HP:0010554" + ], + "webbed finger": [ + "HP:0010554" + ], + "webbed fingers": [ + "HP:0010554" + ], + "webbed skin of finger": [ + "HP:0010554" + ], + "webbed skin of fingers": [ + "HP:0010554" + ], + "overlap finger": [ + "HP:0010557" + ], + "overlapping fingers": [ + "HP:0010557" + ], + "abnormality of the clivus": [ + "HP:0010558" + ], + "vertical clivus": [ + "HP:0010559" + ], + "undulate clavicle": [ + "HP:0010560" + ], + "undulate clavicles": [ + "HP:0010560" + ], + "wavy clavicle": [ + "HP:0010560" + ], + "wavy clavicles": [ + "HP:0010560" + ], + "wavy collarbone": [ + "HP:0010560" + ], + "undulate rib": [ + "HP:0010561" + ], + "undulate ribs": [ + "HP:0010561" + ], + "wavy rib": [ + "HP:0010561" + ], + "wavy ribs": [ + "HP:0010561" + ], + "keloid": [ + "HP:0010562" + ], + "keloids": [ + "HP:0010562" + ], + "bifid epiglottis": [ + "HP:0010564" + ], + "aplasia / hypoplasia of the epiglottis": [ + "HP:0010565" + ], + "hamartoma": [ + "HP:0010566" + ], + "y - shape metatarsal": [ + "HP:0010567" + ], + "y - shaped metatarsals": [ + "HP:0010567" + ], + "y - shape long bone of foot": [ + "HP:0010567" + ], + "y - shaped long bone of foot": [ + "HP:0010567" + ], + "hamartoma of the eye": [ + "HP:0010568" + ], + "elevate 7 - dehydrocholesterol": [ + "HP:0010569" + ], + "elevated 7 - dehydrocholesterol": [ + "HP:0010569" + ], + "elevated level of cholesta - 5,7 - dien - 3beta - ol": [ + "HP:0010569" + ], + "elevated levels of cholesta - 5,7 - dien - 3beta - ol": [ + "HP:0010569" + ], + "low maternal serum alpha - fetoprotein": [ + "HP:0010570" + ], + "elevated level of phytanic acid": [ + "HP:0010571" + ], + "elevated levels of phytanic acid": [ + "HP:0010571" + ], + "abnormality of the epiphysis of the femoral head": [ + "HP:0010574" + ], + "abnormality of the end part of the innermost thighbone": [ + "HP:0010574" + ], + "abnormality of the proximal femoral epiphysis": [ + "HP:0010574" 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epiphyses": [ + "HP:0010580" + ], + "widen , distorted epiphysis": [ + "HP:0010580" + ], + "widened , distorted epiphyses": [ + "HP:0010580" + ], + "irregular epiphysis": [ + "HP:0010582" + ], + "irregular epiphyses": [ + "HP:0010582" + ], + "irregular end part of long bone": [ + "HP:0010582" + ], + "ivory epiphysis": [ + "HP:0010583" + ], + "ivory epiphyses": [ + "HP:0010583" + ], + "epiphyseal sclerosis": [ + "HP:0010583" + ], + "increase bone density in end part of bone": [ + "HP:0010583" + ], + "increased bone density in end part of bone": [ + "HP:0010583" + ], + "pseudoepiphyses": [ + "HP:0010584" + ], + "small epiphysis": [ + "HP:0010585" + ], + "small epiphyses": [ + "HP:0010585" + ], + "small end part of bone": [ + "HP:0010585" + ], + "triangular epiphysis": [ + "HP:0010587" + ], + "triangular epiphyses": [ + "HP:0010587" + ], + "triangular end part of bone": [ + "HP:0010587" + ], + "premature epimetaphyseal fusion": [ + "HP:0010588" + ], + "premature closure of epiphysis": [ + "HP:0010588" + ], + "premature closure of epiphyses": [ + "HP:0010588" + ], + "abnormality of the distal femoral epiphysis": [ + "HP:0010590" + ], + "abnormality of the end part of the outermost thighbone": [ + "HP:0010590" + ], + "abnormality of the proximal tibial epiphysis": [ + "HP:0010591" + ], + "abnormality of the end part of innermost shankbone": [ + "HP:0010591" + ], + "abnormality of the end part of innermost shinbone": [ + "HP:0010591" + ], + "abnormality of the distal tibial epiphysis": [ + "HP:0010592" + ], + "abnormality of the end part of outermost shankbone": [ + "HP:0010592" + ], + "abnormality of the end part of outermost shinbone": [ + "HP:0010592" + ], + "abnormality of fibular epiphysis": [ + "HP:0010593" + ], + "abnormality of fibular epiphyses": [ + "HP:0010593" + ], + "abnormality of the end part of the calf bone": [ + "HP:0010593" + ], + "abnormality of the proximal fibular epiphysis": [ + "HP:0010594" + ], + "abnormality of the innermost end part of calf bone": [ + "HP:0010594" + ], + "abnormality of the distal fibular epiphysis": [ + "HP:0010595" + ], + "abnormality of the outermost end part of calf bone": [ + "HP:0010595" + ], + "abnormality of the proximal radial epiphysis": [ + "HP:0010596" + ], + "abnormality of the distal radial epiphysis": [ + "HP:0010597" + ], + "abnormality of the proximal humeral epiphysis": [ + "HP:0010598" + ], + "abnormality of the end part of the innermost long bone in upper arm": [ + "HP:0010598" + ], + "abnormality of the distal humeral epiphysis": [ + "HP:0010599" + ], + "abnormality of the end part of the outermost long bone in upper arm": [ + "HP:0010599" + ], + "abnormality of the distal ulnar epiphysis": [ + "HP:0010600" + ], + "abnormality of the proximal ulnar epiphysis": [ + "HP:0010601" + ], + "type 2 muscle fiber predominance": [ + "HP:0010602" + ], + "type 2 muscle fibre predominance": [ + "HP:0010602" + ], + "type ii muscle fiber predominance": [ + "HP:0010602" + ], + "type ii muscle fibre predominance": [ + "HP:0010602" + ], + "odontogenic keratocysts of the jaw": [ + "HP:0010603" + ], + "keratocystic odontogenic tumor": [ + "HP:0010603" + ], + "keratocystic odontogenic tumour": [ + "HP:0010603" + ], + "keratocysts of the jaw": [ + "HP:0010603" + ], + "cyst of the eyelid": [ + "HP:0010604" + ], + "eyelid bump": [ + "HP:0010604" + ], + "eyelid mass": [ + "HP:0010604" + ], + "lesion of the eyelid": [ + "HP:0010604" + ], + "chalazion": [ + "HP:0010605" + ], + "meibomian gland lipogranuloma": [ + "HP:0010605" + ], + "hordeolum": [ + "HP:0010606" + ], + "red bump on eyelid": [ + "HP:0010606" + ], + "stye of eyelid": [ + "HP:0010606" + ], + "hordeolum externum": [ + "HP:0010607" + ], + "hordeolum internum": [ + "HP:0010608" + ], + "red bump on inner eyelid": [ + "HP:0010608" + ], + "stye of inner eyelid": [ + "HP:0010608" + ], + "skin tag": [ + "HP:0010609" + ], + "skin tags": [ + "HP:0010609" + ], + "acrochorda": [ + "HP:0010609" + ], + "palmar pit": [ + "HP:0010610" + ], + "palmar pits": [ + "HP:0010610" + ], + "plantar pit": [ + "HP:0010612" + ], + "plantar pits": [ + "HP:0010612" + ], + "fibroma": [ + "HP:0010614" + ], + "angiofibromas": [ + "HP:0010615" + ], + "lung fibroma": [ + "HP:0010616" + ], + "cardiac fibroma": [ + "HP:0010617" + ], + "ovarian fibroma": [ + "HP:0010618" + ], + "fibroadenoma of the breast": [ + "HP:0010619" + ], + "breast fibroadenoma": [ + "HP:0010619" + ], + "breast fibroadenomas": [ + "HP:0010619" + ], + "breast fibroadenosis": [ + "HP:0010619" + ], + "fibroadenosis - breast": [ + "HP:0010619" + ], + "fibroadenosis of breast": [ + "HP:0010619" + ], + "malar prominence": [ + "HP:0010620" + ], + "hyperplasia of malar bone": [ + "HP:0010620" + ], + "hyperplasia of malar bones": [ + "HP:0010620" + ], + "malar excess": [ + "HP:0010620" + ], + "malar hyperplasia": [ + "HP:0010620" + ], + "prominent malar region": [ + "HP:0010620" + ], + "cutaneous syndactyly of toe": [ + "HP:0010621" + ], + "cutaneous syndactyly of toes": [ + "HP:0010621" + ], + "cutaneous syndactyly of foot": [ + "HP:0010621" + ], + "cutaneous syndactyly of feet": [ + "HP:0010621" + ], + "soft tissue syndactyly of toe": [ + "HP:0010621" + ], + "soft tissue syndactyly of toes": [ + "HP:0010621" + ], + "webbed skin of toe": [ + "HP:0010621" + ], + "webbed skin of toes": [ + "HP:0010621" + ], + "neoplasm of the skeletal system": [ + "HP:0010622" + ], + "bone neoplasm": [ + "HP:0010622" + ], + "neoplasia of the skeletal system": [ + "HP:0010622" + ], + "skeletal tumor": [ + "HP:0010622" + ], + "skeletal tumour": [ + "HP:0010622" + ], + "aplastic / hypoplastic toenail": [ + "HP:0010624" + ], + "absent / small toenail": [ + "HP:0010624" + ], + "absent / small toenails": [ + "HP:0010624" + ], + "absent / underdevelop toenail": [ + "HP:0010624" + ], + "absent / underdeveloped toenails": [ + "HP:0010624" + ], + "aplastic / hypoplastic toenails": [ + "HP:0010624" + ], + "hypoplastic - absent toenail": [ + "HP:0010624" + ], + "hypoplastic - absent toenails": [ + "HP:0010624" + ], + "anterior pituitary dysgenesis": [ + "HP:0010625" + ], + "adenohypophysis": [ + "HP:0010625" + ], + "anterior pituitary agenesis": [ + "HP:0010626" + ], + "absent pituitary gland": [ + "HP:0010626" + ], + "aplasia of the pituitary gland": [ + "HP:0010626" + ], + "anterior pituitary hypoplasia": [ + "HP:0010627" + ], + "hypoplasia of the pituitary gland": [ + "HP:0010627" + ], + "underdeveloped pituitary gland": [ + "HP:0010627" + ], + "facial palsy": [ + "HP:0010628" + ], + "bell 's palsy": [ + "HP:0010628" + ], + "cranial nerve vii palsy": [ + "HP:0010628" + ], + "facial muscle weakness of muscle innervate by cn vii": [ + "HP:0010628" + ], + "facial muscle weakness of muscles innervated by cn vii": [ + "HP:0010628" + ], + "facial nerve palsy": [ + "HP:0010628" + ], + "facial nerve paralysis": [ + "HP:0010628" + ], + "facial palsy , unilateral or bilateral": [ + "HP:0010628" + ], + "seventh cranial nerve palsy": [ + "HP:0010628" + ], + "vii th cranial nerve palsy": [ + "HP:0010628" + ], + "abnormal morphology of the cortex of the humerus": [ + "HP:0010629" + ], + "abnormality of metatarsal epiphysis": [ + "HP:0010630" + ], + "abnormality of end part of long bone of foot": [ + "HP:0010630" + ], + "abnormality of the epiphysis of the metatarsal": [ + "HP:0010630" + ], + "abnormality of the epiphyses of the metatarsals": [ + "HP:0010630" + ], + "abnormality of the epiphysis of the foot": [ + "HP:0010631" + ], + "abnormality of the epiphyses of the feet": [ + "HP:0010631" + ], + "abnormality of the end part of the foot bone": [ + "HP:0010631" + ], + "total anosmia": [ + "HP:0010632" + ], + "partial anosmia": [ + "HP:0010633" + ], + "total hyposmia": [ + "HP:0010634" + ], + "partial hyposmia": [ + "HP:0010635" + ], + "schizencephaly": [ + "HP:0010636" + ], + "conjunctival amyloidosis": [ + "HP:0010637" + ], + "elevate alkaline phosphatase of hepatic origin": [ + "HP:0010638" + ], + "elevated alkaline phosphatase of hepatic origin": [ + "HP:0010638" + ], + "elevate alp of hepatic origin": [ + "HP:0010638" + ], + "elevated alp of hepatic origin": [ + "HP:0010638" + ], + "elevate alkaline phosphatase of bone origin": [ + "HP:0010639" + ], + "elevated alkaline phosphatase of bone origin": [ + "HP:0010639" + ], + "elevate alp of bone origin": [ + "HP:0010639" + ], + "elevated alp of bone origin": [ + "HP:0010639" + ], + "increase serum bone - specific alkaline phosphatase": [ + "HP:0010639" + ], + "increased serum bone - specific alkaline phosphatase": [ + "HP:0010639" + ], + "abnormality of the nasal cavity": [ + "HP:0010640" + ], + "abnormality of the midnasal cavity": [ + "HP:0010641" + ], + "midnasal atresia": [ + "HP:0010643" + ], + "midnasal stenosis": [ + "HP:0010644" + ], + "midnasal atresia or stenosis": [ + "HP:0010644" + ], + "aplasia of the distal phalanx of the toe": [ + "HP:0010645" + ], + "aplasia of the distal phalanges of the toes": [ + "HP:0010645" + ], + "absent outermost bone of the toe": [ + "HP:0010645" + ], + "absent outermost bone of the toes": [ + "HP:0010645" + ], + "cervical spine instability": [ + "HP:0010646" + ], + "abnormal elasticity of skin": [ + "HP:0010647" + ], + "dermal translucency": [ + "HP:0010648" + ], + "translucent skin": [ + "HP:0010648" + ], + "flat nasal ala": [ + "HP:0010649" + ], + "flat nasal alae": [ + "HP:0010649" + ], + "depress nasal ala": [ + "HP:0010649" + ], + "depressed nasal alae": [ + "HP:0010649" + ], + "flat nasal alar cartilage": [ + "HP:0010649" + ], + "hypoplasia of the premaxilla": [ + "HP:0010650" + ], + "decreased size of premaxilla": [ + "HP:0010650" + ], + "decreased size of the primary palate bone": [ + "HP:0010650" + ], + "hypoplasia of the intermaxillary bone": [ + "HP:0010650" + ], + "hypoplasia of the primary palate bone": [ + "HP:0010650" + ], + "premaxillary bone deficiency": [ + "HP:0010650" + ], + "premaxillary bone retrusion": [ + "HP:0010650" + ], + "premaxillary retrusion": [ + "HP:0010650" + ], + "premaxillary underdevelopment": [ + "HP:0010650" + ], + "primary palate bone deficiency": [ + "HP:0010650" + ], + "primary palate bone retrusion": [ + "HP:0010650" + ], + "small premaxilla": [ + "HP:0010650" + ], + "small primary palate bone": [ + "HP:0010650" + ], + "underdevelopment of premaxilla": [ + "HP:0010650" + ], + "underdevelopment of the premaxilla": [ + "HP:0010650" + ], + "underdevelopment of the primary palate bone": [ + "HP:0010650" + ], + "abnormal meningeal morphology": [ + "HP:0010651" + ], + "abnormality of the meninges": [ + "HP:0010651" + ], + "abnormal dura mater morphology": [ + "HP:0010652" + ], + "abnormality of the dura mater": [ + "HP:0010652" + ], + "abnormality of the falx cerebri": [ + "HP:0010653" + ], + "abnormality of the cerebral falx": [ + "HP:0010653" + ], + "aplasia of the falx cerebri": [ + "HP:0010654" + ], + "absent cerebral falx": [ + "HP:0010654" + ], + "epiphyseal stipple": [ + "HP:0010655" + ], + "epiphyseal stippling": [ + "HP:0010655" + ], + "epiphyseal punctate calcification": [ + "HP:0010655" + ], + "epiphyseal punctate calcifications": [ + "HP:0010655" + ], + "speckled calcification in end part of bone": [ + "HP:0010655" + ], + "speckled calcifications in end part of bone": [ + "HP:0010655" + ], + "stipple epiphysis": [ + "HP:0010655" + ], + "stippled epiphyses": [ + "HP:0010655" + ], + "stippling of the epiphysis": [ + "HP:0010655" + ], + "stippling of the epiphyses": [ + "HP:0010655" + ], + "abnormal epiphyseal ossification": [ + "HP:0010656" + ], + "abnormal maturation of the end part of a bone": [ + "HP:0010656" + ], + "abnormality of the mineralisation or ossification of the epiphysis": [ + "HP:0010656" + ], + "abnormality of the mineralisation or ossification of the epiphyses": [ + "HP:0010656" + ], + "patchy reduction of bone mineral density": [ + "HP:0010657" + ], + "patchy change of bone mineral density": [ + "HP:0010658" + ], + "patchy changes of bone mineral density": [ + "HP:0010658" + ], + "patchy variation in bone mineral density": [ + "HP:0010659" + ], + "patchy increase and decrease bone mineral density": [ + "HP:0010659" + ], + "patchy increased and decreased bone mineral density": [ + "HP:0010659" + ], + "abnormal hand bone ossification": [ + "HP:0010660" + ], + "abnormal maturation of the hand bone": [ + "HP:0010660" + ], + "abnormal maturation of the hand bones": [ + "HP:0010660" + ], + "abnormal ossification of hand bone": [ + "HP:0010660" + ], + "abnormal ossification of hand bones": [ + "HP:0010660" + ], + "abnormality of the mineralisation and ossification of bone of the hand": [ + "HP:0010660" + ], + "abnormality of the mineralisation and ossification of bones of the hand": [ + "HP:0010660" + ], + "absence of the third cerebral ventricle": [ + "HP:0010661" + ], + "abnormality of the diencephalon": [ + "HP:0010662" + ], + "abnormality of thalamus morphology": [ + "HP:0010663" + ], + "abnormal shape of thalamus": [ + "HP:0010663" + ], + "abnormality of the thalamus": [ + "HP:0010663" + ], + "fusion of the left and right thalamus": [ + "HP:0010664" + ], + "fusion of the left and right thalami": [ + "HP:0010664" + ], + "fuse thalamus": [ + "HP:0010664" + ], + "fused thalami": [ + "HP:0010664" + ], + "fusion of thamali": [ + "HP:0010664" + ], + "undivided thalamus": [ + "HP:0010664" + ], + "undivided thalami": [ + "HP:0010664" + ], + "bilateral coxa valga": [ + "HP:0010665" + ], + "hypoplasia of the anterior nasal spine": [ + "HP:0010666" + ], + "decreased length of anterior nasal spine": [ + "HP:0010666" + ], + "decreased projection of anterior nasal spine": [ + "HP:0010666" + ], + "decreased size of anterior nasal spine": [ + "HP:0010666" + ], + "deficiency of anterior nasal spine": [ + "HP:0010666" + ], + "hypotrophic anterior nasal spine": [ + "HP:0010666" + ], + "small anterior nasal spine": [ + "HP:0010666" + ], + "underdevelopment of anterior nasal spine": [ + "HP:0010666" + ], + "aplasia of the maxilla": [ + "HP:0010667" + ], + "absence of the maxilla": [ + "HP:0010667" + ], + "absence of upper jaw bone": [ + "HP:0010667" + ], + "absence of upper jaw bones": [ + "HP:0010667" + ], + "agenesis of the maxilla": [ + "HP:0010667" + ], + "aplasia of the upper jaw bone": [ + "HP:0010667" + ], + "aplasia of the upper jaw bones": [ + "HP:0010667" + ], + "failure of development of maxilla": [ + "HP:0010667" + ], + "failure of development of upper jaw bone": [ + "HP:0010667" + ], + "failure of development of upper jaw bones": [ + "HP:0010667" + ], + "miss upper jaw bone": [ + "HP:0010667" + ], + "missing upper jaw bones": [ + "HP:0010667" + ], + "abnormality of the zygomatic bone": [ + "HP:0010668" + ], + "abnormality of the cheekbone": [ + "HP:0010668" + ], + "anomaly of the zygomatic bone": [ + "HP:0010668" + ], + "deformity of the cheekbone": [ + "HP:0010668" + ], + "deformity of the zygomatic bone": [ + "HP:0010668" + ], + "malformation of the zygomatic bone": [ + "HP:0010668" + ], + "hypoplasia of the zygomatic bone": [ + "HP:0010669" + ], + "cheekbone underdevelopment": [ + "HP:0010669" + ], + "decreased size of cheekbone": [ + "HP:0010669" + ], + "decreased size of zygomatic bone": [ + "HP:0010669" + ], + "depressed cheekbone": [ + "HP:0010669" + ], + "depress zygomatic bone": [ + "HP:0010669" + ], + "depressed zygomatic bone": [ + "HP:0010669" + ], + "flattening of the zygomatic bone": [ + "HP:0010669" + ], + "hypoplasia of cheekbone": [ + "HP:0010669" + ], + "hypotrophic cheekbone": [ + "HP:0010669" + ], + "hypotrophic zygomatic bone": [ + "HP:0010669" + ], + "hypotrophy of the cheekbone": [ + "HP:0010669" + ], + "hypotrophy of the zygomatic bone": [ + "HP:0010669" + ], + "small cheekbone": [ + "HP:0010669" + ], + "small malar bone": [ + "HP:0010669" + ], + "small zygomatic bone": [ + "HP:0010669" + ], + "underdevelopment of cheekbone": [ + "HP:0010669" + ], + "underdevelopment of zygomatic bone": [ + "HP:0010669" + ], + "abnormality of the third metatarsal bone": [ + "HP:0010672" + ], + "abnormality of the 3rd long bone of foot": [ + "HP:0010672" + ], + "abnormality of the curvature of the vertebral column": [ + "HP:0010674" + ], + "abnormal curve of the backbone": [ + "HP:0010674" + ], + "abnormal curve of the spine": [ + "HP:0010674" + ], + "abnormal curving of the spine": [ + "HP:0010674" + ], + "curvature of spine": [ + "HP:0010674" + ], + "curve spine": [ + "HP:0010674" + ], + "curved spine": [ + "HP:0010674" + ], + "abnormal foot bone ossification": [ + "HP:0010675" + ], + "abnormal maturation of foot bone": [ + "HP:0010675" + ], + "abnormal maturation of foot bones": [ + "HP:0010675" + ], + "abnormal ossification involve bone of the foot": [ + "HP:0010675" + ], + "abnormal ossification involving bones of the feet": [ + "HP:0010675" + ], + "abnormality of the mineralisation and ossification of bone of the foot": [ + "HP:0010675" + ], + "abnormality of the mineralisation and ossification of bones of the feet": [ + "HP:0010675" + ], + "mechanical ileus": [ + "HP:0010676" + ], + "enuresis nocturna": [ + "HP:0010677" + ], + "nocturnal enuresis": [ + "HP:0010677" + ], + "enuresis diurna": [ + "HP:0010678" + ], + "elevate tissue non - specific alkaline phosphatase": [ + "HP:0010679" + ], + "elevated tissue non - specific alkaline phosphatase": [ + "HP:0010679" + ], + "elevate alkaline phosphatase , liver / bone / kidney": [ + "HP:0010679" + ], + "elevated alkaline phosphatase , liver / bone / kidney": [ + "HP:0010679" + ], + "elevate tissue non - specific alp": [ + "HP:0010679" + ], + "elevated tissue non - specific alp": [ + "HP:0010679" + ], + "elevate alkaline phosphatase of renal origin": [ + "HP:0010680" + ], + "elevated alkaline phosphatase of renal origin": [ + "HP:0010680" + ], + "elevate alp of renal origin": [ + "HP:0010680" + ], + "elevated alp of renal origin": [ + "HP:0010680" + ], + "elevate intestinal alkaline phosphatase": [ + "HP:0010681" + ], + "elevated intestinal alkaline phosphatase": [ + "HP:0010681" + ], + "elevate intestinal alp": [ + "HP:0010681" + ], + "elevated intestinal alp": [ + "HP:0010681" + ], + "elevate placental alkaline phosphatase": [ + "HP:0010682" + ], + "elevated placental alkaline phosphatase": [ + "HP:0010682" + ], + "elevate placental alp": [ + "HP:0010682" + ], + "elevated placental alp": [ + "HP:0010682" + ], + "low tissue non - specific alkaline phosphatase": [ + "HP:0010683" + ], + "low tissue non - specific alp": [ + "HP:0010683" + ], + "low alkaline phosphatase of bone origin": [ + "HP:0010684" + ], + "low alp of bone origin": [ + "HP:0010684" + ], + "low alkaline phosphatase of renal origin": [ + "HP:0010685" + ], + "low alp of renal origin": [ + "HP:0010685" + ], + "low alkaline phosphatase of hepatic origin": [ + "HP:0010686" + ], + "low alp of hepatic origin": [ + "HP:0010686" + ], + "low intestinal alkaline phosphatase": [ + "HP:0010687" + ], + "low intestinal alp": [ + "HP:0010687" + ], + "low placental alkaline phosphatase": [ + "HP:0010688" + ], + "low placental alp": [ + "HP:0010688" + ], + "mirror image polydactyly": [ + "HP:0010689" + ], + "mirror image duplication of digit": [ + "HP:0010689" + ], + "mirror image duplication of digits": [ + "HP:0010689" + ], + "mirror image hand polydactyly": [ + "HP:0010690" + ], + "mirror image dupliction of finger": [ + "HP:0010690" + ], + "mirror image dupliction of fingers": [ + "HP:0010690" + ], + "mirror image foot polydactyly": [ + "HP:0010691" + ], + "mirror image dupliction of toe": [ + "HP:0010691" + ], + "mirror image dupliction of toes": [ + "HP:0010691" + ], + "2 - 5 finger syndactyly": [ + "HP:0010692" + ], + "web 2nd - 5th finger": [ + "HP:0010692" + ], + "webbed 2nd - 5th fingers": [ + "HP:0010692" + ], + "webbed index , middle and little finger": [ + "HP:0010692" + ], + "webbed index , middle and pinkie finger": [ + "HP:0010692" + ], + "webbed index , middle and pinky finger": [ + "HP:0010692" + ], + "pulverulent cataract": [ + "HP:0010693" + ], + "lamellar pulverulent cataract": [ + "HP:0010694" + ], + "sutural cataract": [ + "HP:0010695" + ], + "polar cataract": [ + "HP:0010696" + ], + "anterior pyramidal cataract": [ + "HP:0010697" + ], + "pyramidal cataract": [ + "HP:0010697" + ], + "nuclear pulverulent cataract": [ + "HP:0010698" + ], + "cataracta pulverulenta centralis": [ + "HP:0010698" + ], + "central pulverulent cataract": [ + "HP:0010698" + ], + "coppock - like cataract": [ + "HP:0010698" + ], + "pulverulent nuclear cataract": [ + "HP:0010698" + ], + "triangular nuclear cataract": [ + "HP:0010699" + ], + "obsolete total cataract": [ + "HP:0010700" + ], + "abnormal immunoglobulin level": [ + "HP:0010701" + ], + "abnormal immunoglobulin concentration": [ + "HP:0010701" + ], + "abnormal serum immunoglobulin concentration": [ + "HP:0010701" + ], + "abnormal serum immunoglobulin level": [ + "HP:0010701" + ], + "abnormal serum immunoglobulin levels": [ + "HP:0010701" + ], + "abnormal serum level of immunoglobulin": [ + "HP:0010701" + ], + "immunoglobulin abnormality": [ + "HP:0010701" + ], + "increase circulate antibody level": [ + "HP:0010702" + ], + "increased circulating antibody level": [ + "HP:0010702" + ], + "elevate immunoglobulin level": [ + "HP:0010702" + ], + "elevated immunoglobulin levels": [ + "HP:0010702" + ], + "hypergammaglobulinaemia": [ + "HP:0010702" + ], + "hypergammaglobulinemia": [ + "HP:0010702" + ], + "hyperglobulinemia": [ + "HP:0010702" + ], + "increase antibody level in blood": [ + "HP:0010702" + ], + "increased antibody level in blood": [ + "HP:0010702" + ], + "increase gamma globulin": [ + "HP:0010702" + ], + "increased gamma globulin": [ + "HP:0010702" + ], + "increase immunoglobulin level": [ + "HP:0010702" + ], + "increased immunoglobulin level": [ + "HP:0010702" + ], + "increase serum gamma globulin": [ + "HP:0010702" + ], + "increased serum gamma globulin": [ + "HP:0010702" + ], + "raise immunoglobulin level": [ + "HP:0010702" + ], + "raised immunoglobulin levels": [ + "HP:0010702" + ], + "1 - 2 finger syndactyly": [ + "HP:0010704" + ], + "web 1st - 2nd finger": [ + "HP:0010704" + ], + "webbed 1st - 2nd finger": [ + "HP:0010704" + ], + "web thumb and index finger": [ + "HP:0010704" + ], + "webbed thumb and index finger": [ + "HP:0010704" + ], + "4 - 5 finger syndactyly": [ + "HP:0010705" + ], + "web 4th - 5th finger": [ + "HP:0010705" + ], + "webbed 4th - 5th finger": [ + "HP:0010705" + ], + "1 - 3 finger syndactyly": [ + "HP:0010706" + ], + "web 1st - 3rd finger": [ + "HP:0010706" + ], + "webbed 1st - 3rd finger": [ + "HP:0010706" + ], + "1 - 4 finger syndactyly": [ + "HP:0010707" + ], + "web 1st - 4th finger": [ + "HP:0010707" + ], + "webbed 1st - 4th finger": [ + "HP:0010707" + ], + "1 - 5 finger syndactyly": [ + "HP:0010708" + ], + "web 1 - 5 finger": [ + "HP:0010708" + ], + "webbed 1 - 5 fingers": [ + "HP:0010708" + ], + "web 1st - 5th finger": [ + "HP:0010708" + ], + "webbed 1st - 5th fingers": [ + "HP:0010708" + ], + "2 - 4 finger syndactyly": [ + "HP:0010709" + ], + "syndactyly of second to fourth finger": [ + "HP:0010709" + ], + "syndactyly of second to fourth fingers": [ + "HP:0010709" + ], + "webbed index through ring finger": [ + "HP:0010709" + ], + "webbed index through ring fingers": [ + "HP:0010709" + ], + "3 - 5 finger syndactyly": [ + "HP:0010710" + ], + "webbed third , fourth and fifth toe": [ + "HP:0010710" + ], + "webbed third , fourth and fifth toes": [ + "HP:0010710" + ], + "1 - 2 toe syndactyly": [ + "HP:0010711" + ], + "web 1st - 2nd toe": [ + "HP:0010711" + ], + "webbed 1st - 2nd toes": [ + "HP:0010711" + ], + "web first and second toe": [ + "HP:0010711" + ], + "webbed first and second toes": [ + "HP:0010711" + ], + "1 - 4 toe syndactyly": [ + "HP:0010712" + ], + "web first through fourth toe": [ + "HP:0010712" + ], + "webbed first through fourth toes": [ + "HP:0010712" + ], + "1 - 5 toe syndactyly": [ + "HP:0010713" + ], + "syndactyly of all toe": [ + "HP:0010713" + ], + "syndactyly of all toes": [ + "HP:0010713" + ], + "web 1st - 5th toe": [ + "HP:0010713" + ], + "webbed 1st - 5th toes": [ + "HP:0010713" + ], + "2 - 4 toe syndactyly": [ + "HP:0010714" + ], + "syndactyly of toe 2 , 3 and 4": [ + "HP:0010714" + ], + "syndactyly of toes 2 , 3 and 4": [ + "HP:0010714" + ], + "syndactyly toe 2 - 4": [ + "HP:0010714" + ], + "syndactyly toes 2 - 4": [ + "HP:0010714" + ], + "web 2nd - 4th toe": [ + "HP:0010714" + ], + "webbed 2nd - 4th toes": [ + "HP:0010714" + ], + "2 - 5 toe syndactyly": [ + "HP:0010715" + ], + "web 2nd - 5th toe": [ + "HP:0010715" + ], + "webbed 2nd - 5th toes": [ + "HP:0010715" + ], + "3 - 5 toe syndactyly": [ + "HP:0010716" + ], + "web 3rd - 5th toe": [ + "HP:0010716" + ], + "webbed 3rd - 5th toes": [ + "HP:0010716" + ], + "osseous syndactyly of toe": [ + "HP:0010717" + ], + "osseous syndactyly of toes": [ + "HP:0010717" + ], + "osseous syndactyly of the toe": [ + "HP:0010717" + ], + "osseous syndactyly of the toes": [ + "HP:0010717" + ], + "abnormality of hair texture": [ + "HP:0010719" + ], + "abnormality of hair consistency": [ + "HP:0010719" + ], + "abnormality of hair curl pattern": [ + "HP:0010719" + ], + "abnormality of hair volume": [ + "HP:0010719" + ], + "abnormal hair pattern": [ + "HP:0010720" + ], + "abnormal distribution of hair": [ + "HP:0010720" + ], + "abnormal hair whorl": [ + "HP:0010721" + ], + "abnormal hair whorls": [ + "HP:0010721" + ], + "abnormal whorl of hair": [ + "HP:0010721" + ], + "asymmetry of the ear": [ + "HP:0010722" + ], + "asymmetry of the ears": [ + "HP:0010722" + ], + "asymmetric ear": [ + "HP:0010722" + ], + "asymmetric ears": [ + "HP:0010722" + ], + "cystic lesion of the pinna": [ + "HP:0010723" + ], + "cystic lesions of the pinnae": [ + "HP:0010723" + ], + "advanced pneumatization of the mastoid process": [ + "HP:0010724" + ], + "prominent corneal nerve fiber": [ + "HP:0010726" + ], + "prominent corneal nerve fibers": [ + "HP:0010726" + ], + "prominent corneal nerve fibre": [ + "HP:0010726" + ], + "prominent corneal nerve fibres": [ + "HP:0010726" + ], + "visible corneal nerve fiber": [ + "HP:0010726" + ], + "visible corneal nerve fibers": [ + "HP:0010726" + ], + "visible corneal nerve fibre": [ + "HP:0010726" + ], + "visible corneal nerve fibres": [ + "HP:0010726" + ], + "spontaneous rupture of the globe": [ + "HP:0010727" + ], + "aplasia of the retina": [ + "HP:0010728" + ], + "absent retina": [ + "HP:0010728" + ], + "cherry red spot of the macula": [ + "HP:0010729" + ], + "macular cherry red spot": [ + "HP:0010729" + ], + "double eyebrow": [ + "HP:0010730" + ], + "duplication of eyebrow": [ + "HP:0010730" + ], + "extension of eyebrow towards upper eyelid": [ + "HP:0010731" + ], + "extension of eyebrows towards upper eyelid": [ + "HP:0010731" + ], + "nodular change affect the eyelid": [ + "HP:0010732" + ], + "nodular changes affecting the eyelids": [ + "HP:0010732" + ], + "eyelid nodule": [ + "HP:0010732" + ], + "eyelid nodules": [ + "HP:0010732" + ], + "naevus flammeus of the eyelid": [ + "HP:0010733" + ], + "port - wine stain on eyelid": [ + "HP:0010733" + ], + "fibrous dysplasia of the bone": [ + "HP:0010734" + ], + "fibrous dysplasia of the bones": [ + "HP:0010734" + ], + "polyostotic fibrous dysplasia": [ + "HP:0010735" + ], + "monostotic fibrous dysplasia": [ + "HP:0010736" + ], + "osteopoikilosis": [ + "HP:0010739" + ], + "osteopathia striata": [ + "HP:0010740" + ], + "pedal edema": [ + "HP:0010741" + ], + "dependant edema": [ + "HP:0010741" + ], + "dependant oedema": [ + "HP:0010741" + ], + "edema of the low limb": [ + "HP:0010741" + ], + "edema of the lower limbs": [ + "HP:0010741" + ], + "fluid accumulation in low limb": [ + "HP:0010741" + ], + "fluid accumulation in lower limbs": [ + "HP:0010741" + ], + "leg edema": [ + "HP:0010741" + ], + "leg oedema": [ + "HP:0010741" + ], + "low leg swell": [ + "HP:0010741" + ], + "lower leg swelling": [ + "HP:0010741" + ], + "oedema of the low limb": [ + "HP:0010741" + ], + "oedema of the lower limbs": [ + "HP:0010741" + ], + "pedal oedema": [ + "HP:0010741" + ], + "peripheral edema of low extremity": [ + "HP:0010741" + ], + "peripheral edema of lower extremity": [ + "HP:0010741" + ], + "peripheral oedema of low extremity": [ + "HP:0010741" + ], + "peripheral oedema of lower extremity": [ + "HP:0010741" + ], + "edema of the upper limb": [ + "HP:0010742" + ], + "edema of the upper limbs": [ + "HP:0010742" + ], + "fluid accumulation in upper limb": [ + "HP:0010742" + ], + "fluid accumulation in upper limbs": [ + "HP:0010742" + ], + "oedema of the upper limb": [ + "HP:0010742" + ], + "oedema of the upper limbs": [ + "HP:0010742" + ], + "short metatarsal": [ + "HP:0010743" + ], + "hypoplasia of the metatarsal bone": [ + "HP:0010743" + ], + "hypoplasia of the metatarsal bones": [ + "HP:0010743" + ], + "hypoplastic metatarsal": [ + "HP:0010743" + ], + "hypoplastic metatarsals": [ + "HP:0010743" + ], + "short long bone of foot": [ + "HP:0010743" + ], + "short metatarsal bone": [ + "HP:0010743" + ], + "short metatarsal bones": [ + "HP:0010743" + ], + "short metatarsals": [ + "HP:0010743" + ], + "shorten metatarsal": [ + "HP:0010743" + ], + "shortened metatarsals": [ + "HP:0010743" + ], + "absent metatarsal bone": [ + "HP:0010744" + ], + "absent long bone of foot": [ + "HP:0010744" + ], + "aplasia of the metatarsal bone": [ + "HP:0010744" + ], + "aplasia of the metatarsal bones": [ + "HP:0010744" + ], + "aplasia of the phalanx of the toe": [ + "HP:0010745" + ], + "aplasia of the phalanges of the toes": [ + "HP:0010745" + ], + "absent bone of the toe": [ + "HP:0010745" + ], + "absent bones of the toes": [ + "HP:0010745" + ], + "aphalangia of the toe": [ + "HP:0010745" + ], + "aphalangia of the toes": [ + "HP:0010745" + ], + "hypoplasia of the phalanx of the toe": [ + "HP:0010746" + ], + "hypoplasia of the phalanges of the toes": [ + "HP:0010746" + ], + "small toe bone": [ + "HP:0010746" + ], + "small toe bones": [ + "HP:0010746" + ], + "medial flaring of the eyebrow": [ + "HP:0010747" + ], + "ectopic lacrimal punctum": [ + "HP:0010748" + ], + "abnormal position of the lacrimal punctum": [ + "HP:0010748" + ], + "blepharochalasis": [ + "HP:0010749" + ], + "saggy upper eyelid skin": [ + "HP:0010749" + ], + "dermatochalasis": [ + "HP:0010750" + ], + "baggy eye": [ + "HP:0010750" + ], + "baggy eyes": [ + "HP:0010750" + ], + "droopy eyelid skin": [ + "HP:0010750" + ], + "extra eyelid skin": [ + "HP:0010750" + ], + "eyelid dermatochalasia": [ + "HP:0010750" + ], + "hooding of eyelid": [ + "HP:0010750" + ], + "hooding of eyelids": [ + "HP:0010750" + ], + "redundant eyelid skin": [ + "HP:0010750" + ], + "dimple chin": [ + "HP:0010751" + ], + "chin butt": [ + "HP:0010751" + ], + "chin dent": [ + "HP:0010751" + ], + "chin dimple": [ + "HP:0010751" + ], + "chin dimples": [ + "HP:0010751" + ], + "chin skin dimple": [ + "HP:0010751" + ], + "gelasin of chin": [ + "HP:0010751" + ], + "indentation of chin": [ + "HP:0010751" + ], + "cleft mandible": [ + "HP:0010752" + ], + "cleft lower jaw": [ + "HP:0010752" + ], + "mandibular cleft": [ + "HP:0010752" + ], + "midline defect of mandible": [ + "HP:0010753" + ], + "midline cleft of mandible": [ + "HP:0010753" + ], + "abnormality of the temporomandibular joint": [ + "HP:0010754" + ], + "abnormality of the jaw joint": [ + "HP:0010754" + ], + "anomaly of the temporomandibular joint": [ + "HP:0010754" + ], + "deformity of the jaw joint": [ + "HP:0010754" + ], + "deformity of the temporomandibular joint": [ + "HP:0010754" + ], + "derangement of the temporomandibular joint": [ + "HP:0010754" + ], + "malformation of jaw joint": [ + "HP:0010754" + ], + "malformation of the temporomandibular joint": [ + "HP:0010754" + ], + "asymmetry of the maxilla": [ + "HP:0010755" + ], + "asymmetry of right and leave side of the maxilla": [ + "HP:0010755" + ], + "asymmetry of right and left side of the maxilla": [ + "HP:0010755" + ], + "asymmetry of the upper jaw": [ + "HP:0010755" + ], + "asymmetry of upper jaw": [ + "HP:0010755" + ], + "cant maxilla": [ + "HP:0010755" + ], + "canted maxilla": [ + "HP:0010755" + ], + "cant upper jaw": [ + "HP:0010755" + ], + "canted upper jaw": [ + "HP:0010755" + ], + "crook maxilla": [ + "HP:0010755" + ], + "crooked maxilla": [ + "HP:0010755" + ], + "crook upper jaw": [ + "HP:0010755" + ], + "crooked upper jaw": [ + "HP:0010755" + ], + "deviation of the maxilla": [ + "HP:0010755" + ], + "deviation of the upper jaw": [ + "HP:0010755" + ], + "tilt maxilla": [ + "HP:0010755" + ], + "tilted maxilla": [ + "HP:0010755" + ], + "tilt upper jaw": [ + "HP:0010755" + ], + "tilted upper jaw": [ + "HP:0010755" + ], + "unequal side of maxilla": [ + "HP:0010755" + ], + "unequal sides of maxilla": [ + "HP:0010755" + ], + "uneven maxilla": [ + "HP:0010755" + ], + "uneven upper jaw": [ + "HP:0010755" + ], + "aplasia / hypoplasia of the premaxilla": [ + "HP:0010756" + ], + "aplasia / hypoplasia of the intermaxillary bone": [ + "HP:0010756" + ], + "aplasia / hypoplasia of the primary palate bone": [ + "HP:0010756" + ], + "aplasia of the premaxilla": [ + "HP:0010757" + ], + "absence of the intermaxillary bone": [ + "HP:0010757" + ], + "absence of the premaxilla": [ + "HP:0010757" + ], + "absence of the primary palate bone": [ + "HP:0010757" + ], + "aplasia of the intermaxillary bone": [ + "HP:0010757" + ], + "aplasia of the primary palate bone": [ + "HP:0010757" + ], + "failure of development of premaxilla": [ + "HP:0010757" + ], + "failure of development of the primary palate bone": [ + "HP:0010757" + ], + "miss premaxilla": [ + "HP:0010757" + ], + "missing premaxilla": [ + "HP:0010757" + ], + "miss primary palate bone": [ + "HP:0010757" + ], + "missing primary palate bone": [ + "HP:0010757" + ], + "abnormality of the premaxilla": [ + "HP:0010758" + ], + "abnormality of the intermaxillary bone": [ + "HP:0010758" + ], + "abnormality of the intermaxillary segment of the maxilla": [ + "HP:0010758" + ], + "abnormality of the premaxillary bone": [ + "HP:0010758" + ], + "abnormality of the primary palate bone": [ + "HP:0010758" + ], + "prominence of the premaxilla": [ + "HP:0010759" + ], + "anterior position of the premaxilla": [ + "HP:0010759" + ], + "anterior position of the primary palate bone": [ + "HP:0010759" + ], + "premaxillary bone excess": [ + "HP:0010759" + ], + "prominence of the intermaxillary bone": [ + "HP:0010759" + ], + "prominence of the primary palate bone": [ + "HP:0010759" + ], + "absent toe": [ + "HP:0010760" + ], + "absent toes": [ + "HP:0010760" + ], + "aplasia of the toe": [ + "HP:0010760" + ], + "aplasia of the toes": [ + "HP:0010760" + ], + "aplasia of toe": [ + "HP:0010760" + ], + "broad columella": [ + "HP:0010761" + ], + "columella , broad": [ + "HP:0010761" + ], + "columella , wide": [ + "HP:0010761" + ], + "fullness of columella": [ + "HP:0010761" + ], + "hyperplasia of columella": [ + "HP:0010761" + ], + "increase width of columella": [ + "HP:0010761" + ], + "increased width of columella": [ + "HP:0010761" + ], + "chordoma": [ + "HP:0010762" + ], + "low insertion of columella": [ + "HP:0010763" + ], + "ala high than columella": [ + "HP:0010763" + ], + "ala higher than columella": [ + "HP:0010763" + ], + "columella , low insertion": [ + "HP:0010763" + ], + "short eyelash": [ + "HP:0010764" + ], + "short eyelashes": [ + "HP:0010764" + ], + "decreased length of eyelash": [ + "HP:0010764" + ], + "decreased length of eyelashes": [ + "HP:0010764" + ], + "palmar hyperkeratosis": [ + "HP:0010765" + ], + "ectopic calcification": [ + "HP:0010766" + ], + "sacrococcygeal pilonidal abnormality": [ + "HP:0010767" + ], + "pilonidal sinus": [ + "HP:0010769" + ], + "pilonidal cyst": [ + "HP:0010769" + ], + "pilonidal fistula": [ + "HP:0010770" + ], + "pilonidal abscess": [ + "HP:0010771" + ], + "sacrococcygeal fistula": [ + "HP:0010771" + ], + "anomalous pulmonary venous return": [ + "HP:0010772" + ], + "partial anomalous pulmonary venous return": [ + "HP:0010773" + ], + "partial anomalous pulmonary venous connection": [ + "HP:0010773" + ], + "cor triatriatum": [ + "HP:0010774" + ], + "triatrial heart": [ + "HP:0010774" + ], + "vascular ring": [ + "HP:0010775" + ], + "vascular ring of aorta": [ + "HP:0010775" + ], + "tracheobronchmegaly": [ + "HP:0010776" + ], + "bronchomegaly": [ + "HP:0010777" + ], + "tracheomegaly": [ + "HP:0010778" + ], + "large pelvis bone": [ + "HP:0010779" + ], + "large pelvis": [ + "HP:0010779" + ], + "hyperacusis": [ + "HP:0010780" + ], + "loudness intolerance": [ + "HP:0010780" + ], + "sensitivity to noise": [ + "HP:0010780" + ], + "skin dimple": [ + "HP:0010781" + ], + "skin dimples": [ + "HP:0010781" + ], + "shoulder dimple": [ + "HP:0010782" + ], + "acromial dimple": [ + "HP:0010782" + ], + "bi - acromial dimple": [ + "HP:0010782" + ], + "bi - acromial dimples": [ + "HP:0010782" + ], + "shoulder dimples": [ + "HP:0010782" + ], + "erythema": [ + "HP:0010783" + ], + "redness of skin or mucous membrane": [ + "HP:0010783" + ], + "uterine neoplasm": [ + "HP:0010784" + ], + "uterine cancer": [ + "HP:0010784" + ], + "uterine neoplasia": [ + "HP:0010784" + ], + "uterine tumor": [ + "HP:0010784" + ], + "uterine tumour": [ + "HP:0010784" + ], + "gonadal neoplasm": [ + "HP:0010785" + ], + "gonadal neoplasia": [ + "HP:0010785" + ], + "urinary tract neoplasm": [ + "HP:0010786" + ], + "urinary tract neoplasia": [ + "HP:0010786" + ], + "genital neoplasm": [ + "HP:0010787" + ], + "genital neoplasia": [ + "HP:0010787" + ], + "genital tumor": [ + "HP:0010787" + ], + "genital tumour": [ + "HP:0010787" + ], + "testicular neoplasm": [ + "HP:0010788" + ], + "testicular cancer": [ + "HP:0010788" + ], + "testicular neoplasia": [ + "HP:0010788" + ], + "testicular tumor": [ + "HP:0010788" + ], + "testicular tumour": [ + "HP:0010788" + ], + "abnormality of the leydig cell": [ + "HP:0010789" + ], + "abnormality of the leydig cells": [ + "HP:0010789" + ], + "hyoplasia of the leydig cell": [ + "HP:0010790" + ], + "hyoplasia of the leydig cells": [ + "HP:0010790" + ], + "hyperplasia of the leydig cell": [ + "HP:0010791" + ], + "hyperplasia of the leydig cells": [ + "HP:0010791" + ], + "bifid nail": [ + "HP:0010793" + ], + "duplicate nail": [ + "HP:0010793" + ], + "duplicated nail": [ + "HP:0010793" + ], + "notch nail": [ + "HP:0010793" + ], + "notched nail": [ + "HP:0010793" + ], + "impaired visuospatial constructive cognition": [ + "HP:0010794" + ], + "cerebellar glioma": [ + "HP:0010795" + ], + "brainstem glioma": [ + "HP:0010796" + ], + "hemangioblastoma": [ + "HP:0010797" + ], + "haemangioblastoma": [ + "HP:0010797" + ], + "lip freckle": [ + "HP:0010798" + ], + "ephelis of lip": [ + "HP:0010798" + ], + "labial lentigo": [ + "HP:0010798" + ], + "lip lentigo": [ + "HP:0010798" + ], + "pinealoma": [ + "HP:0010799" + ], + "absent cupid 's bow": [ + "HP:0010800" + ], + "agenesis of cupid 's bow": [ + "HP:0010800" + ], + "aplasia of cupid 's bow": [ + "HP:0010800" + ], + "failure of development of cupid 's bow": [ + "HP:0010800" + ], + "lack of cupid 's bow": [ + "HP:0010800" + ], + "miss cupid 's bow": [ + "HP:0010800" + ], + "missing cupid 's bow": [ + "HP:0010800" + ], + "underdeveloped nasolabial fold": [ + "HP:0010801" + ], + "flat nasolabial fold": [ + "HP:0010801" + ], + "nasolabial crease , hypoplastic": [ + "HP:0010801" + ], + "nasolabial crease , underdevelop": [ + "HP:0010801" + ], + "nasolabial crease , underdeveloped": [ + "HP:0010801" + ], + "nasolabial fold , hypoplastic": [ + "HP:0010801" + ], + "shallow nasolabial fold": [ + "HP:0010801" + ], + "perioral hyperpigmentation": [ + "HP:0010802" + ], + "darkening of skin around the mouth": [ + "HP:0010802" + ], + "increase pigmentation around the mouth": [ + "HP:0010802" + ], + "increased pigmentation around the mouth": [ + "HP:0010802" + ], + "evert upper lip vermilion": [ + "HP:0010803" + ], + "everted upper lip vermilion": [ + "HP:0010803" + ], + "droop upper lip": [ + "HP:0010803" + ], + "drooping upper lip": [ + "HP:0010803" + ], + "eclabium of upper lip": [ + "HP:0010803" + ], + "evert prominent upper lip": [ + "HP:0010803" + ], + "everted prominent upper lip": [ + "HP:0010803" + ], + "evert upper lip": [ + "HP:0010803" + ], + "everted upper lip": [ + "HP:0010803" + ], + "outward turn upper lip": [ + "HP:0010803" + ], + "outward turned upper lip": [ + "HP:0010803" + ], + "protrude upper lip": [ + "HP:0010803" + ], + "protruding upper lip": [ + "HP:0010803" + ], + "tent upper lip vermilion": [ + "HP:0010804" + ], + "tented upper lip vermilion": [ + "HP:0010804" + ], + "invert v - shape upper lip": [ + "HP:0010804" + ], + "inverted v - shaped upper lip": [ + "HP:0010804" + ], + "tent mouth": [ + "HP:0010804" + ], + "tented mouth": [ + "HP:0010804" + ], + "tent upper lip": [ + "HP:0010804" + ], + "tented upper lip": [ + "HP:0010804" + ], + "upturned corner of mouth": [ + "HP:0010805" + ], + "upturned corners of mouth": [ + "HP:0010805" + ], + "upturned mouth": [ + "HP:0010805" + ], + "upturned oral commisures": [ + "HP:0010805" + ], + "u - shape upper lip vermilion": [ + "HP:0010806" + ], + "u - shaped upper lip vermilion": [ + "HP:0010806" + ], + "carp - like mouth": [ + "HP:0010806" + ], + "carp - shape mouth": [ + "HP:0010806" + ], + "carp - shaped mouth": [ + "HP:0010806" + ], + "fish mouth": [ + "HP:0010806" + ], + "large , carp - shape mouth": [ + "HP:0010806" + ], + "large , carp - shaped mouth": [ + "HP:0010806" + ], + "wide , carp - shape mouth": [ + "HP:0010806" + ], + "wide , carp - shaped mouth": [ + "HP:0010806" + ], + "open bite": [ + "HP:0010807" + ], + "absence of overlap of upper and low teeth": [ + "HP:0010807" + ], + "absence of overlap of upper and lower teeth": [ + "HP:0010807" + ], + "open bite between upper and low teeth": [ + "HP:0010807" + ], + "open bite between upper and lower teeth": [ + "HP:0010807" + ], + "protrude tongue": [ + "HP:0010808" + ], + "protruding tongue": [ + "HP:0010808" + ], + "lingual prolapse": [ + "HP:0010808" + ], + "lingual prominence": [ + "HP:0010808" + ], + "lingual protrusion": [ + "HP:0010808" + ], + "prolapse of tongue": [ + "HP:0010808" + ], + "prominent tongue": [ + "HP:0010808" + ], + "tongue protrusion": [ + "HP:0010808" + ], + "tongue stick out of mouth": [ + "HP:0010808" + ], + "tongue sticking out of mouth": [ + "HP:0010808" + ], + "broad uvula": [ + "HP:0010809" + ], + "wide uvula": [ + "HP:0010809" + ], + "long uvula": [ + "HP:0010810" + ], + "elongate uvula": [ + "HP:0010810" + ], + "elongated uvula": [ + "HP:0010810" + ], + "hyperplasia of uvula": [ + "HP:0010810" + ], + "long palatine uvula": [ + "HP:0010810" + ], + "narrow uvula": [ + "HP:0010811" + ], + "narrow palatine uvula": [ + "HP:0010811" + ], + "thin uvula": [ + "HP:0010811" + ], + "short uvula": [ + "HP:0010812" + ], + "blunt uvula": [ + "HP:0010812" + ], + "hypoplastic uvula": [ + "HP:0010812" + ], + "short palatine uvula": [ + "HP:0010812" + ], + "abnormal number of hair whorl": [ + "HP:0010813" + ], + "abnormal number of hair whorls": [ + "HP:0010813" + ], + "abnormal number of hair swirl": [ + "HP:0010813" + ], + "abnormal number of hair 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"abnormality of the nervus trigeminus": [ + "HP:0010824" + ], + "abnormality of the eleventh cranial nerve": [ + "HP:0010825" + ], + "abnormality of cranial nerve xi": [ + "HP:0010825" + ], + "abnormality of the accessory nerve": [ + "HP:0010825" + ], + "abnormality of the twelfth cranial nerve": [ + "HP:0010826" + ], + "abnormality of cranial nerve 12": [ + "HP:0010826" + ], + "abnormality of cranial nerve xii": [ + "HP:0010826" + ], + "abnormality of the hypoglossal nerve": [ + "HP:0010826" + ], + "abnormality of the seventh cranial nerve": [ + "HP:0010827" + ], + "abnormality of the facial nerve": [ + "HP:0010827" + ], + "hemifacial spasm": [ + "HP:0010828" + ], + "hemifacial spasms": [ + "HP:0010828" + ], + "spasm on one side of the face": [ + "HP:0010828" + ], + "spasms on one side of the face": [ + "HP:0010828" + ], + "impaired temperature sensation": [ + "HP:0010829" + ], + "abnormality of temperature sensation": [ + "HP:0010829" + ], + "impaired thermal sensitivity": [ + 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"eeg with spike - wave complex ( > 3.5 hz )": [ + "HP:0010849" + ], + "eeg with spike - wave complexes ( > 3.5 hz )": [ + "HP:0010849" + ], + "eeg with 3 - 4 - hz spike wave": [ + "HP:0010849" + ], + "eeg with 3 - 4 - hz spike waves": [ + "HP:0010849" + ], + "eeg with spike - wave complex": [ + "HP:0010850" + ], + "eeg with spike - wave complexes": [ + "HP:0010850" + ], + "eeg with burst suppression": [ + "HP:0010851" + ], + "eeg with photoparoxysmal response": [ + "HP:0010852" + ], + "photoparoxysmal response on eeg": [ + "HP:0010852" + ], + "eeg with periodic lateralize epileptiform discharge": [ + "HP:0010853" + ], + "eeg with periodic lateralized epileptiform discharges": [ + "HP:0010853" + ], + "eeg : periodic lateralized epileptiform discharge": [ + "HP:0010853" + ], + "eeg : periodic lateralized epileptiform discharges": [ + "HP:0010853" + ], + "eeg with generalized low amplitude activity": [ + "HP:0010854" + ], + "eeg with generalised low amplitude activity": [ + "HP:0010854" + ], + "eeg : generalise low amplitude activity": [ + "HP:0010854" + ], + "eeg : generalised low amplitude activity": [ + "HP:0010854" + ], + "eeg with localized low amplitude activity": [ + "HP:0010855" + ], + "eeg with localised low amplitude activity": [ + "HP:0010855" + ], + "eeg : localise low amplitude activity": [ + "HP:0010855" + ], + "eeg : localised low amplitude activity": [ + "HP:0010855" + ], + "eeg with periodic complex": [ + "HP:0010856" + ], + "eeg with periodic complexes": [ + "HP:0010856" + ], + "eeg : periodic complex": [ + "HP:0010856" + ], + "eeg : periodic complexes": [ + "HP:0010856" + ], + "radermecker complex": [ + "HP:0010856" + ], + "radermecker complexes": [ + "HP:0010856" + ], + "eeg with periodic abnormality": [ + "HP:0010857" + ], + "eeg with periodic abnormalities": [ + "HP:0010857" + ], + "eeg : periodic abnormality": [ + "HP:0010857" + ], + "eeg : periodic abnormalities": [ + "HP:0010857" + ], + "eeg with hyperventilation - induced epileptiform discharge": [ + "HP:0010858" + ], + "eeg with hyperventilation - induced epileptiform discharges": [ + "HP:0010858" + ], + "frank breech presentation": [ + "HP:0010859" + ], + "complete breech presentation": [ + "HP:0010860" + ], + "incomplete breech presentation": [ + "HP:0010861" + ], + "delay fine motor development": [ + "HP:0010862" + ], + "delayed fine motor development": [ + "HP:0010862" + ], + "receptive language delay": [ + "HP:0010863" + ], + "intellectual disability , severe": [ + "HP:0010864" + ], + "early and severe mental retardation": [ + "HP:0010864" + ], + "mental retardation , severe": [ + "HP:0010864" + ], + "severe mental retardation": [ + "HP:0010864" + ], + "oppositional defiant disorder": [ + "HP:0010865" + ], + "abdominal wall defect": [ + "HP:0010866" + ], + "congenital anterior abdominal wall defect": [ + "HP:0010866" + ], + "dyssynergia": [ + "HP:0010867" + ], + "ocular dyssynergia": [ + "HP:0010868" + ], + "asynergia": [ + "HP:0010869" + ], + "sensory ataxia": [ + "HP:0010871" + ], + "afferent ataxia": [ + "HP:0010871" + ], + "ataxia , sensory": [ + "HP:0010871" + ], + "spinal ataxia": [ + "HP:0010871" + ], + "t - wave inversion": [ + "HP:0010872" + ], + "ekg : t - wave inversion": [ + "HP:0010872" + ], + "cervical spinal cord atrophy": [ + "HP:0010873" + ], + "tendon xanthomatosis": [ + "HP:0010874" + ], + "tendon xanthoma": [ + "HP:0010874" + ], + "tendon xanthomas": [ + "HP:0010874" + ], + "chaddock reflex": [ + "HP:0010875" + ], + "abnormal circulate protein concentration": [ + "HP:0010876" + ], + "abnormal circulating protein concentration": [ + "HP:0010876" + ], + "abnormal circulate protein level": [ + "HP:0010876" + ], + "abnormal circulating protein level": [ + "HP:0010876" + ], + "abnormality of circulate protein level": [ + "HP:0010876" + ], + "abnormality of circulating protein level": [ + "HP:0010876" + ], + "blood protein disease": [ + "HP:0010876" + ], + "serum protein abnormality": [ + "HP:0010876" + ], + "monocular strabismus": [ + "HP:0010877" + ], + "unilateral strabismus": [ + "HP:0010877" + ], + "fetal cystic hygroma": [ + "HP:0010878" + ], + "foetal cystic hygroma": [ + "HP:0010878" + ], + "postnatal cystic hygroma": [ + "HP:0010879" + ], + "increase nuchal translucency": [ + "HP:0010880" + ], + "increased nuchal translucency": [ + "HP:0010880" + ], + "abnormality of the umbilical cord": [ + "HP:0010881" + ], + "umbilical cord issue": [ + "HP:0010881" + ], + "pulmonary valve atresia": [ + "HP:0010882" + ], + "aortic valve atresia": [ + "HP:0010883" + ], + "aortic atresia": [ + "HP:0010883" + ], + "acromelia": [ + "HP:0010884" + ], + "avascular necrosis": [ + "HP:0010885" + ], + "aseptic bone necrosis": [ + "HP:0010885" + ], + "aseptic necrosis": [ + "HP:0010885" + ], + "bone infarction": [ + "HP:0010885" + ], + "death of bone due to decreased blood supply": [ + "HP:0010885" + ], + "ischaemic bone necrosis": [ + "HP:0010885" + ], + "ischemic bone necrosis": [ + "HP:0010885" + ], + "osteochondronecrosis": [ + "HP:0010885" + ], + "osteonecrosis": [ + "HP:0010885" + ], + "osteochondritis dissecans": [ + "HP:0010886" + ], + "osteochondrosis dissecans": [ + "HP:0010886" + ], + "morbus koehler": [ + "HP:0010888" + ], + "morbus kienboeck": [ + "HP:0010889" + ], + "kienboeck 's disease": [ + "HP:0010889" + ], + "kienb\u00f6ck 's disease": [ + "HP:0010889" + ], + "lunatomalacia": [ + "HP:0010889" + ], + "morbus osgood - schlatter": [ + "HP:0010890" + ], + "osgood schlatter disease": [ + "HP:0010890" + ], + "morbus scheuermann": [ + "HP:0010891" + ], + "calve disease": [ + "HP:0010891" + ], + "juvenile osteochondrosis of the spine": [ + "HP:0010891" + ], + "scheuermann disease": [ + "HP:0010891" + ], + "scheuermann kyphosis": [ + "HP:0010891" + ], + "sherman 's disease": [ + "HP:0010891" + ], + "abnormal circulate branch chain amino acid concentration": [ + "HP:0010892" + ], + "abnormal circulating branched chain amino acid concentration": [ + "HP:0010892" + ], + "abnormal circulate phenylalanine concentration": [ + "HP:0010893" + ], + "abnormal circulating phenylalanine concentration": [ + "HP:0010893" + ], + "abnormality of phenylalanine metabolism": [ + "HP:0010893" + ], + "abnormal circulate serine family amino acid concentration": [ + "HP:0010894" + ], + "abnormal circulating serine family amino acid concentration": [ + "HP:0010894" + ], + "abnormality of serine family amino acid metabolism": [ + "HP:0010894" + ], + "abnormal circulate glycine concentration": [ + "HP:0010895" + ], + "abnormal circulating glycine concentration": [ + "HP:0010895" + ], + "hypersarcosinemia": [ + "HP:0010896" + ], + "high plasma sarcosine level": [ + "HP:0010896" + ], + "high plasma sarcosine levels": [ + "HP:0010896" + ], + "hypersarcosinuria": [ + "HP:0010897" + ], + "high urine sarcosine level": [ + "HP:0010897" + ], + "high urine sarcosine levels": [ + "HP:0010897" + ], + "abnormal circulate sarcosine concentration": [ + "HP:0010898" + ], + "abnormal circulating sarcosine concentration": [ + "HP:0010898" + ], + "abnormal circulate aspartate family amino acid concentration": [ + "HP:0010899" + ], + "abnormal circulating aspartate family amino acid concentration": [ + "HP:0010899" + ], + "abnormal circulate threonine concentration": [ + "HP:0010900" + ], + "abnormal circulating threonine concentration": [ + "HP:0010900" + ], + "abnormality of threonine metabolism": [ + "HP:0010900" + ], + "abnormal circulate methionine concentration": [ + "HP:0010901" + ], + "abnormal circulating methionine concentration": [ + "HP:0010901" + ], + "abnormality of methionine metabolism": [ + "HP:0010901" + ], + "abnormal circulate glutamine family amino acid concentration": [ + "HP:0010902" + ], + "abnormal circulating glutamine family amino acid concentration": [ + "HP:0010902" + ], + "abnormal circulate glutamine concentration": [ + "HP:0010903" + ], + "abnormal circulating glutamine concentration": [ + "HP:0010903" + ], + "abnormal circulate histidine concentration": [ + "HP:0010904" + ], + "abnormal circulating histidine concentration": [ + "HP:0010904" + ], + "abnormality of histidine metabolism": [ + "HP:0010904" + ], + "obsolete abnormality of histidine metabolism": [ + "HP:0010905" + ], + "hyperhistidinemia": [ + "HP:0010906" + ], + "high blood histidine level": [ + "HP:0010906" + ], + "histidinemia": [ + "HP:0010906" + ], + "abnormal circulate proline concentration": [ + "HP:0010907" + ], + "abnormal circulating proline concentration": [ + "HP:0010907" + ], + "abnormal circulate lysine concentration": [ + "HP:0010908" + ], + "abnormal circulating lysine concentration": [ + "HP:0010908" + ], + "abnormality of lysine metabolism": [ + "HP:0010908" + ], + "abnormal circulate arginine concentration": [ + "HP:0010909" + ], + "abnormal circulating arginine concentration": [ + "HP:0010909" + ], + "abnormality of arginine metabolism": [ + "HP:0010909" + ], + "hypervalinemia": [ + "HP:0010910" + ], + "high blood valine concentration": [ + "HP:0010910" + ], + "hyperleucinemia": [ + "HP:0010911" + ], + "high blood leucine concentration": [ + "HP:0010911" + ], + "abnormal circulate isoleucine concentration": [ + "HP:0010912" + ], + "abnormal circulating isoleucine concentration": [ + "HP:0010912" + ], + "hyperisoleucinemia": [ + "HP:0010913" + ], + "high blood isoleucine concentration": [ + "HP:0010913" + ], + "abnormal circulate valine concentration": [ + "HP:0010914" + ], + "abnormal circulating valine concentration": [ + "HP:0010914" + ], + "abnormality of valine metabolism": [ + "HP:0010914" + ], + "abnormal circulate pyruvate family amino acid concentration": [ + "HP:0010915" + ], + "abnormal circulating pyruvate family amino acid concentration": [ + "HP:0010915" + ], + "abnormality of pyruvate family amino acid metabolism": [ + "HP:0010915" + ], + "abnormal circulate alanine concentration": [ + "HP:0010916" + ], + "abnormal circulating alanine concentration": [ + "HP:0010916" + ], + "abnormality of alanine metabolism": [ + "HP:0010916" + ], + "abnormal circulate tyrosine concentration": [ + "HP:0010917" + ], + "abnormal circulating tyrosine concentration": [ + "HP:0010917" + ], + "abnormal circulate cysteine concentration": [ + "HP:0010918" + ], + "abnormal circulating cysteine concentration": [ + "HP:0010918" + ], + "abnormal circulate homocysteine concentration": [ + "HP:0010919" + ], + "abnormal circulating homocysteine concentration": [ + "HP:0010919" + ], + "zonular cataract": [ + "HP:0010920" + ], + "coralliform cataract": [ + "HP:0010921" + ], + "membranous cataract": [ + "HP:0010922" + ], + "anterior subcapsular cataract": [ + "HP:0010923" + ], + "posterior cortical cataract": [ + "HP:0010924" + ], + "nuclear punctate cataract": [ + "HP:0010925" + ], + "aculeiform cataract": [ + "HP:0010926" + ], + "fasciculiform cataract": [ + "HP:0010926" + ], + "frost cataract": [ + "HP:0010926" + ], + "frosted cataract": [ + "HP:0010926" + ], + "needle - shape cataract": [ + "HP:0010926" + ], + "needle - shaped cataract": [ + "HP:0010926" + ], + "abnormal blood inorganic cation concentration": [ + "HP:0010927" + ], + "abnormality of divalent inorganic cation homeostasis": [ + "HP:0010927" + ], + "obsolete increase urinary orotic acid concentration": [ + "HP:0010928" + ], + "obsolete increased urinary orotic acid concentration": [ + "HP:0010928" + ], + "abnormal blood cation concentration": [ + "HP:0010929" + ], + "abnormality of cation homeostasis": [ + "HP:0010929" + ], + "abnormal blood monovalent inorganic cation concentration": [ + "HP:0010930" + ], + "abnormality of monovalent inorganic cation homeostasis": [ + "HP:0010930" + ], + "abnormal blood sodium concentration": [ + "HP:0010931" + ], + "abnormal blood na+ level": [ + "HP:0010931" + ], + "abnormal blood na+ levels": [ + "HP:0010931" + ], + "abnormal circulate na concentration": [ + "HP:0010931" + ], + "abnormal circulating na concentration": [ + "HP:0010931" + ], + "abnormality of sodium 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"HP:0010963" + ], + "abnormal circulate long - chain fatty - acid concentration": [ + "HP:0010964" + ], + "abnormal circulating long - chain fatty - acid concentration": [ + "HP:0010964" + ], + "abnormal circulate phytanic acid concentration": [ + "HP:0010965" + ], + "abnormal circulating phytanic acid concentration": [ + "HP:0010965" + ], + "abnormal circulate phytanic acid level": [ + "HP:0010965" + ], + "abnormal circulating phytanic acid level": [ + "HP:0010965" + ], + "abnormal circulate fatty - acid anion concentration": [ + "HP:0010966" + ], + "abnormal circulating fatty - acid anion concentration": [ + "HP:0010966" + ], + "abnormality of fatty acid anion": [ + "HP:0010966" + ], + "abnormal circulate carnitine concentration": [ + "HP:0010967" + ], + "abnormal circulating carnitine concentration": [ + "HP:0010967" + ], + "carnitine level abnormal": [ + "HP:0010967" + ], + "carnitine levels abnormal": [ + "HP:0010967" + ], + "abnormality of liposaccharide metabolism": [ + "HP:0010968" + ], + "abnormality of glycolipid metabolism": [ + "HP:0010969" + ], + "blood group antigen abnormality": [ + "HP:0010970" + ], + "absence of lutheran antigen on erythrocyte": [ + "HP:0010971" + ], + "absence of lutheran antigen on erythrocytes": [ + "HP:0010971" + ], + "anemia of inadequate production": [ + "HP:0010972" + ], + "anaemia of inadequate production": [ + "HP:0010972" + ], + "anemia , dyserythropoietic": [ + "HP:0010972" + ], + "defective erythropoiesis": [ + "HP:0010972" + ], + "dyserythropoietic anaemia": [ + "HP:0010972" + ], + "dyserythropoietic anemia": [ + "HP:0010972" + ], + "ineffective erythropoiesis": [ + "HP:0010972" + ], + "abnormal myeloid leukocyte morphology": [ + "HP:0010974" + ], + "abnormality of myeloid leukocyte": [ + "HP:0010974" + ], + "abnormality of myeloid leukocytes": [ + "HP:0010974" + ], + "abnormal b cell count": [ + "HP:0010975" + ], + "abnormal number of b cell": [ + "HP:0010975" + ], + "abnormal number of b cells": [ + 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"polygenic inheritance": [ + "HP:0010982" + ], + "oligogenic inheritance": [ + "HP:0010983" + ], + "digenic inheritance": [ + "HP:0010984" + ], + "gonosomal inheritance": [ + "HP:0010985" + ], + "abnormal cellular immune system morphology": [ + "HP:0010987" + ], + "abnormality of the extrinsic pathway": [ + "HP:0010988" + ], + "abnormality of the intrinsic pathway": [ + "HP:0010989" + ], + "abnormality of the common coagulation pathway": [ + "HP:0010990" + ], + "abnormal morphology of the abdominal musculature": [ + "HP:0010991" + ], + "abnormality of the abdominal musculature": [ + "HP:0010991" + ], + "stress urinary incontinence": [ + "HP:0010992" + ], + "abnormality of the cerebral subcortex": [ + "HP:0010993" + ], + "abnormality of the cerebral medulla": [ + "HP:0010993" + ], + "abnormal corpus striatum morphology": [ + "HP:0010994" + ], + "abnormality of the neostriatum": [ + "HP:0010994" + ], + "abnormality of the striate nucleus": [ + "HP:0010994" + ], + "abnormality of the striatum": [ + "HP:0010994" + ], + "abnormal circulate dicarboxylic acid concentration": [ + "HP:0010995" + ], + "abnormal circulating dicarboxylic acid concentration": [ + "HP:0010995" + ], + "abnormal circulate monocarboxylic acid cocentration": [ + "HP:0010996" + ], + "abnormal circulating monocarboxylic acid cocentration": [ + "HP:0010996" + ], + "chromosomal breakage induce by ionize radiation": [ + "HP:0010997" + ], + "chromosomal breakage induced by ionizing radiation": [ + "HP:0010997" + ], + "chromosomal breakage induce by ionise radiation": [ + "HP:0010997" + ], + "chromosomal breakage induced by ionising radiation": [ + "HP:0010997" + ], + "increase cellular radiosensitivity": [ + "HP:0010997" + ], + "increased cellular radiosensitivity": [ + "HP:0010997" + ], + "radiation - induced chromosome instability": [ + "HP:0010997" + ], + "increase susceptibility to spontaneous sister chromatid exchange": [ + "HP:0010998" + ], + "increased susceptibility to spontaneous sister 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cellular physiology": [ + "HP:0011017" + ], + "abnormality of cell physiology": [ + "HP:0011017" + ], + "abnormality of the cell cycle": [ + "HP:0011018" + ], + "abnormality of chromosome condensation": [ + "HP:0011019" + ], + "abnormality of mucopolysaccharide metabolism": [ + "HP:0011020" + ], + "abnormality of circulate enzyme level": [ + "HP:0011021" + ], + "abnormality of circulating enzyme level": [ + "HP:0011021" + ], + "abnormal circulating unsaturated fatty acid concentration": [ + "HP:0011022" + ], + "abnormal circulate prostaglandin circulation": [ + "HP:0011023" + ], + "abnormal circulating prostaglandin circulation": [ + "HP:0011023" + ], + "abnormality of the gastrointestinal tract": [ + "HP:0011024" + ], + "abnormality of the gi tract": [ + "HP:0011024" + ], + "digestive system disease": [ + "HP:0011024" + ], + "gastrointestinal disease": [ + "HP:0011024" + ], + "abnormal cardiovascular system physiology": [ + "HP:0011025" + ], + "abnormality of cardiovascular system physiology": [ + "HP:0011025" + ], + "aplasia / hypoplasia of the vagina": [ + "HP:0011026" + ], + "absent / small vagina": [ + "HP:0011026" + ], + "absent / underdevelop vagina": [ + "HP:0011026" + ], + "absent / underdeveloped vagina": [ + "HP:0011026" + ], + "abnormal fallopian tube morphology": [ + "HP:0011027" + ], + "abnormality of the fallopian tube": [ + "HP:0011027" + ], + "abnormality of blood circulation": [ + "HP:0011028" + ], + "blood circulation disorder": [ + "HP:0011028" + ], + "internal hemorrhage": [ + "HP:0011029" + ], + "internal bleeding": [ + "HP:0011029" + ], + "internal haemorrhage": [ + "HP:0011029" + ], + "abnormal blood transition element cation concentration": [ + "HP:0011030" + ], + "abnormality of transition element cation homeostasis": [ + "HP:0011030" + ], + "abnormality of iron homeostasis": [ + "HP:0011031" + ], + "abnormality of fluid regulation": [ + "HP:0011032" + ], + "fluid imbalance": [ + "HP:0011032" + ], + "impairment of fructose metabolism": [ 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], + "abnormal blood potassium concentration": [ + "HP:0011042" + ], + "abnormal blood k concentration": [ + "HP:0011042" + ], + "abnormality of potassium homeostasis": [ + "HP:0011042" + ], + "abnormality of circulate adrenocorticotropin level": [ + "HP:0011043" + ], + "abnormality of circulating adrenocorticotropin level": [ + "HP:0011043" + ], + "abnormality of circulate acth level": [ + "HP:0011043" + ], + "abnormality of circulating acth level": [ + "HP:0011043" + ], + "abnormality of circulate adrenocorticotropic hormone level": [ + "HP:0011043" + ], + "abnormality of circulating adrenocorticotropic hormone level": [ + "HP:0011043" + ], + "abnormality of circulate corticotropin level": [ + "HP:0011043" + ], + "abnormality of circulating corticotropin level": [ + "HP:0011043" + ], + "abnormal number of permanent teeth": [ + "HP:0011044" + ], + "abnormal complement of permanent teeth": [ + "HP:0011044" + ], + "abnormal number of adult teeth": [ + "HP:0011044" + ], + "abnormal number of secondary dentition": [ + "HP:0011044" + ], + "abnormal permanent tooth count": [ + "HP:0011044" + ], + "agenesis of permanent maxillary central incisor": [ + "HP:0011045" + ], + "absence of permanent maxillary central incisor": [ + "HP:0011045" + ], + "absence of permanent upper central incisor": [ + "HP:0011045" + ], + "absence of permanent upper front tooth": [ + "HP:0011045" + ], + "agenesis of adult maxillary central incisor": [ + "HP:0011045" + ], + "failure of development of permanent maxillary central incisor": [ + "HP:0011045" + ], + "miss adult upper central incisor": [ + "HP:0011045" + ], + "missing adult upper central incisor": [ + "HP:0011045" + ], + "miss permanent maxillary central incisor": [ + "HP:0011045" + ], + "missing permanent maxillary central incisor": [ + "HP:0011045" + ], + "miss permanent upper central incisor": [ + "HP:0011045" + ], + "missing permanent upper central incisor": [ + "HP:0011045" + ], + "miss permanent upper front tooth": [ + "HP:0011045" + ], + "missing permanent upper front tooth": [ + "HP:0011045" + ], + "agenesis of primary maxillary central incisor": [ + "HP:0011046" + ], + "absence of deciduous maxillary central incisor": [ + "HP:0011046" + ], + "absence of primary maxillary central incisor": [ + "HP:0011046" + ], + "absence of upper front baby tooth": [ + "HP:0011046" + ], + "agenesis of deciduous maxillary central incisor": [ + "HP:0011046" + ], + "failure of development of deciduous maxillary central incisor": [ + "HP:0011046" + ], + "failure of development of primary maxillary central incisor": [ + "HP:0011046" + ], + "miss deciduous maxillary central incisor": [ + "HP:0011046" + ], + "missing deciduous maxillary central incisor": [ + "HP:0011046" + ], + "miss primary maxillary central incisor": [ + "HP:0011046" + ], + "missing primary maxillary central incisor": [ + "HP:0011046" + ], + "miss upper front baby tooth": [ + "HP:0011046" + ], + "missing upper front baby tooth": [ + "HP:0011046" + ], + "miss upper front milk tooth": [ + "HP:0011046" + ], + "missing upper front milk tooth": [ + "HP:0011046" + ], + "agenesis of primary mandibular central incisor": [ + "HP:0011047" + ], + "absence of deciduous mandibular central incisor": [ + "HP:0011047" + ], + "absence of primary mandibular central incisor": [ + "HP:0011047" + ], + "agenesis of deciduous low central incisor": [ + "HP:0011047" + ], + "agenesis of deciduous lower central incisor": [ + "HP:0011047" + ], + "agenesis of primary low central incisor": [ + "HP:0011047" + ], + "agenesis of primary lower central incisor": [ + "HP:0011047" + ], + "failure of development of deciduous mandibular central incisor": [ + "HP:0011047" + ], + "failure of development of primary mandibular central incisor": [ + "HP:0011047" + ], + "miss deciduous mandibular central incisor": [ + "HP:0011047" + ], + "missing deciduous mandibular central incisor": [ + "HP:0011047" + ], + "miss low central incisor milk tooth": [ + "HP:0011047" + ], + "missing lower central incisor milk tooth": [ + "HP:0011047" + ], + "miss low front baby tooth": [ + "HP:0011047" + ], + "missing lower front baby tooth": [ + "HP:0011047" + ], + "miss low front milk tooth": [ + "HP:0011047" + ], + "missing lower front milk tooth": [ + "HP:0011047" + ], + "miss low front primary tooth": [ + "HP:0011047" + ], + "missing lower front primary tooth": [ + "HP:0011047" + ], + "miss primary mandibular central incisor": [ + "HP:0011047" + ], + "missing primary mandibular central incisor": [ + "HP:0011047" + ], + "agenesis of permanent mandibular central incisor": [ + "HP:0011048" + ], + "absence of permanent low central incisor": [ + "HP:0011048" + ], + "absence of permanent lower central incisor": [ + "HP:0011048" + ], + "absence of permanent low front tooth": [ + "HP:0011048" + ], + "absence of permanent lower front tooth": [ + "HP:0011048" + ], + "absence of permanent mandibular central incisor": [ + "HP:0011048" + ], + "agenesis of adult mandibular central incisor": [ + "HP:0011048" + ], + "failure of development of permanent mandibular central incisor": [ + "HP:0011048" + ], + "miss adult lower central incisor": [ + "HP:0011048" + ], + "missing adult lower central incisor": [ + "HP:0011048" + ], + "miss permanent low central incisor": [ + "HP:0011048" + ], + "missing permanent lower central incisor": [ + "HP:0011048" + ], + "miss permanent low front tooth": [ + "HP:0011048" + ], + "missing permanent lower front tooth": [ + "HP:0011048" + ], + "miss permanent mandibular central incisor": [ + "HP:0011048" + ], + "missing permanent mandibular central incisor": [ + "HP:0011048" + ], + "agenesis of primary maxillary lateral incisor": [ + "HP:0011049" + ], + "absence of deciduous maxillary lateral incisor": [ + "HP:0011049" + ], + "absence of primary maxillary lateral incisor": [ + "HP:0011049" + ], + "agenesis of deciduous maxillary lateral incisor": [ + "HP:0011049" + ], + "failure of development of deciduous maxillary lateral incisor": [ + 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"HP:0011062" + ], + "crook incisor": [ + "HP:0011062" + ], + "crooked incisors": [ + "HP:0011062" + ], + "malposition of incisor": [ + "HP:0011062" + ], + "malposition of incisors": [ + "HP:0011062" + ], + "abnormal incisor morphology": [ + "HP:0011063" + ], + "abnormality of incisor morphology": [ + "HP:0011063" + ], + "abnormality of shape of incisor": [ + "HP:0011063" + ], + "abnormal number of incisor": [ + "HP:0011064" + ], + "abnormal number of incisors": [ + "HP:0011064" + ], + "abnormal number of front teeth": [ + "HP:0011064" + ], + "conical incisor": [ + "HP:0011065" + ], + "cone shape front tooth": [ + "HP:0011065" + ], + "cone shaped front tooth": [ + "HP:0011065" + ], + "conoid incisor": [ + "HP:0011065" + ], + "peg shape front tooth": [ + "HP:0011065" + ], + "peg shaped front tooth": [ + "HP:0011065" + ], + "peg shape incisor": [ + "HP:0011065" + ], + "peg shaped incisors": [ + "HP:0011065" + ], + "peg - shaped incisor": [ + "HP:0011065" + ], + "peg - shaped incisors": [ 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"HP:0011072" + ], + "abnormality of dental color": [ + "HP:0011073" + ], + "abnormality of dental colour": [ + "HP:0011073" + ], + "abnormality of dental shade": [ + "HP:0011073" + ], + "abnormality of tooth color": [ + "HP:0011073" + ], + "abnormality of tooth colour": [ + "HP:0011073" + ], + "abnormality of tooth shade": [ + "HP:0011073" + ], + "localized hypoplasia of dental enamel": [ + "HP:0011074" + ], + "localised dysplasia of tooth enamel": [ + "HP:0011074" + ], + "localised hypoplasia of dental enamel": [ + "HP:0011074" + ], + "localised hypoplasia of tooth enamel": [ + "HP:0011074" + ], + "localized dysplasia of tooth enamel": [ + "HP:0011074" + ], + "localized hypoplasia of tooth enamel": [ + "HP:0011074" + ], + "green teeth": [ + "HP:0011075" + ], + "green color teeth": [ + "HP:0011075" + ], + "green colored teeth": [ + "HP:0011075" + ], + "green colour teeth": [ + "HP:0011075" + ], + "green coloured teeth": [ + "HP:0011075" + ], + "green tooth shade": [ + "HP:0011075" + ], 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"increased size of incisor": [ + "HP:0011081" + ], + "increase width of incisor": [ + "HP:0011081" + ], + "increased width of incisor": [ + "HP:0011081" + ], + "large incisor": [ + "HP:0011081" + ], + "conical primary incisor": [ + "HP:0011082" + ], + "cone shape front baby tooth": [ + "HP:0011082" + ], + "cone shaped front baby tooth": [ + "HP:0011082" + ], + "conical deciduous incisor": [ + "HP:0011082" + ], + "conoid primary incisor": [ + "HP:0011082" + ], + "peg shape front baby tooth": [ + "HP:0011082" + ], + "peg shaped front baby tooth": [ + "HP:0011082" + ], + "peg shape primary incisor": [ + "HP:0011082" + ], + "peg shaped primary incisor": [ + "HP:0011082" + ], + "point front baby tooth": [ + "HP:0011082" + ], + "pointed front baby tooth": [ + "HP:0011082" + ], + "point primary incisor": [ + "HP:0011082" + ], + "pointed primary incisor": [ + "HP:0011082" + ], + "primary front shark tooth": [ + "HP:0011082" + ], + "conical maxillary incisor": [ + "HP:0011083" + ], + "cone shape maxillary incisor": [ + "HP:0011083" + ], + "cone shaped maxillary incisor": [ + "HP:0011083" + ], + "cone shape upper front tooth": [ + "HP:0011083" + ], + "cone shaped upper front tooth": [ + "HP:0011083" + ], + "conoid maxillary incisor": [ + "HP:0011083" + ], + "peg shape upper front tooth": [ + "HP:0011083" + ], + "peg shaped upper front tooth": [ + "HP:0011083" + ], + "point maxillary incisor": [ + "HP:0011083" + ], + "pointed maxillary incisor": [ + "HP:0011083" + ], + "point upper front tooth": [ + "HP:0011083" + ], + "pointed upper front tooth": [ + "HP:0011083" + ], + "upper front shark tooth": [ + "HP:0011083" + ], + "hypocalcification of dental enamel": [ + "HP:0011084" + ], + "decrease enamel calcification": [ + "HP:0011084" + ], + "decreased enamel calcification": [ + "HP:0011084" + ], + "poorly calcify tooth enamel": [ + "HP:0011084" + ], + "poorly calcified tooth enamel": [ + "HP:0011084" + ], + "hypomature dental enamel": [ + "HP:0011085" + ], + "immature tooth enamel": [ + "HP:0011085" + ], + "soft teeth": [ + "HP:0011085" + ], + "soft tooth enamel": [ + "HP:0011085" + ], + "dentinogenesis imperfecta of primary and permanent teeth": [ + "HP:0011086" + ], + "dentinogenesis imperfecta of adult and baby teeth": [ + "HP:0011086" + ], + "dentinogenesis imperfecta of both set of teeth": [ + "HP:0011086" + ], + "dentinogenesis imperfecta of both sets of teeth": [ + "HP:0011086" + ], + "talon cusp": [ + "HP:0011087" + ], + "den evaginatus": [ + "HP:0011087" + ], + "dens evaginatus": [ + "HP:0011087" + ], + "extra cusp on inside of front tooth": [ + "HP:0011087" + ], + "talon cusps": [ + "HP:0011087" + ], + "den in dente": [ + "HP:0011088" + ], + "dens in dente": [ + "HP:0011088" + ], + "den invaginatus": [ + "HP:0011088" + ], + "dens invaginatus": [ + "HP:0011088" + ], + "tooth within a tooth": [ + "HP:0011088" + ], + "double tooth": [ + "HP:0011089" + ], + "conjoin teeth": [ + "HP:0011089" + ], + "conjoined teeth": [ + "HP:0011089" + ], + "teeth , double": [ + "HP:0011089" + ], + "twin tooth": [ + "HP:0011089" + ], + "twinning tooth": [ + "HP:0011089" + ], + "fuse teeth": [ + "HP:0011090" + ], + "fused teeth": [ + "HP:0011090" + ], + "fusion of teeth": [ + "HP:0011090" + ], + "join teeth": [ + "HP:0011090" + ], + "joined teeth": [ + "HP:0011090" + ], + "gemination": [ + "HP:0011091" + ], + "gemination of tooth": [ + "HP:0011091" + ], + "splitting of crown of tooth": [ + "HP:0011091" + ], + "mulberry molar": [ + "HP:0011092" + ], + "syphilitic permanent first molar": [ + "HP:0011092" + ], + "molarization of premolar": [ + "HP:0011093" + ], + "enlarge premolar": [ + "HP:0011093" + ], + "enlarged premolar": [ + "HP:0011093" + ], + "increase size of premolar": [ + "HP:0011093" + ], + "increased size of premolar": [ + "HP:0011093" + ], + "molar shape of bicuspid": [ + "HP:0011093" + ], + "molar shape of premolar": [ + "HP:0011093" + ], + "molarization of bicuspid": [ + "HP:0011093" + ], + "increase overbite": [ + "HP:0011094" + ], + "increased overbite": [ + "HP:0011094" + ], + "deep bite": [ + "HP:0011094" + ], + "deep overbite": [ + "HP:0011094" + ], + "increase overlap of upper and low incisor": [ + "HP:0011094" + ], + "increased overlap of upper and lower incisors": [ + "HP:0011094" + ], + "overbite": [ + "HP:0011094" + ], + "scissors bite": [ + "HP:0011094" + ], + "supraocclusion": [ + "HP:0011094" + ], + "overjet": [ + "HP:0011095" + ], + "abnormality of horizontal incisor relationship": [ + "HP:0011095" + ], + "buck teeth": [ + "HP:0011095" + ], + "protrusion of the maxillary incisor": [ + "HP:0011095" + ], + "protrusion of the maxillary incisors": [ + "HP:0011095" + ], + "protrusion of upper teeth in front of low teeth": [ + "HP:0011095" + ], + "protrusion of upper teeth in front of lower teeth": [ + "HP:0011095" + ], + "upper teeth stick out forward": [ + "HP:0011095" + ], + "upper teeth sticking out forward": [ + "HP:0011095" + ], + "peripheral demyelination": [ + "HP:0011096" + ], + "demyelination": [ + "HP:0011096" + ], + "epileptic spasm": [ + "HP:0011097" + ], + "epileptic spasms": [ + "HP:0011097" + ], + "salaam convulsion": [ + "HP:0011097" + ], + "salaam convulsions": [ + "HP:0011097" + ], + "salaam seizure": [ + "HP:0011097" + ], + "salaam seizures": [ + "HP:0011097" + ], + "west syndrome": [ + "HP:0011097" + ], + "speech apraxia": [ + "HP:0011098" + ], + "apraxia of speech": [ + "HP:0011098" + ], + "verbal dyspraxia": [ + "HP:0011098" + ], + "spastic hemiparesis": [ + "HP:0011099" + ], + "spastic hemiplegia": [ + "HP:0011099" + ], + "intestinal atresia": [ + "HP:0011100" + ], + "ileal atresia": [ + "HP:0011102" + ], + "abnormal leave ventricular outflow tract morphology": [ + "HP:0011103" + ], + "abnormal left ventricular outflow tract morphology": [ + "HP:0011103" + ], + "abnormality of the left ventricular outflow tract": [ + "HP:0011103" + ], + "abnormality of blood volume homeostasis": [ + "HP:0011104" + ], + "hypervolemia": [ + "HP:0011105" + ], + "fluid overload in blood": [ + "HP:0011105" + ], + "hypovolemia": [ + "HP:0011106" + ], + "deplete blood volume": [ + "HP:0011106" + ], + "depleted blood volume": [ + "HP:0011106" + ], + "recurrent aphthous stomatitis": [ + "HP:0011107" + ], + "aphthous stomatitis": [ + "HP:0011107" + ], + "buccal aphthous ulcer": [ + "HP:0011107" + ], + "buccal aphthous ulcers": [ + "HP:0011107" + ], + "recurrent aphthous ulcer": [ + "HP:0011107" + ], + "recurrent aphthous ulcers": [ + "HP:0011107" + ], + "recurrent canker sore": [ + "HP:0011107" + ], + "recurrent canker sores": [ + "HP:0011107" + ], + "recurrent oral aphthae": [ + "HP:0011107" + ], + "recurrent sinusitis": [ + "HP:0011108" + ], + "recurrent sinus disease": [ + "HP:0011108" + ], + "sinusitis , recurrent": [ + "HP:0011108" + ], + "chronic sinusitis": [ + "HP:0011109" + ], + "chronic sinus disease": [ + "HP:0011109" + ], + "sinusitis , chronic": [ + "HP:0011109" + ], + "recurrent tonsillitis": [ + "HP:0011110" + ], + "recurrent inflammation of tonsil": [ 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"HP:0011119" + ], + "abnormal morphology of dorsum of nose": [ + "HP:0011119" + ], + "abnormality of the dorsum of nose": [ + "HP:0011119" + ], + "abnormality of the nasal ridge": [ + "HP:0011119" + ], + "anomaly of the nasal ridge": [ + "HP:0011119" + ], + "crook dorsum of nose": [ + "HP:0011119" + ], + "crooked dorsum of nose": [ + "HP:0011119" + ], + "crook nasal dorsum": [ + "HP:0011119" + ], + "crooked nasal dorsum": [ + "HP:0011119" + ], + "crook nasal ridge": [ + "HP:0011119" + ], + "crooked nasal ridge": [ + "HP:0011119" + ], + "deformity of the dorsum of the nose": [ + "HP:0011119" + ], + "deformity of the nasal dorsum": [ + "HP:0011119" + ], + "deformity of the nasal ridge": [ + "HP:0011119" + ], + "malformation of the dorsum of nose": [ + "HP:0011119" + ], + "malformation of the nasal dorsum": [ + "HP:0011119" + ], + "malformation of the nasal ridge": [ + "HP:0011119" + ], + "concave nasal ridge": [ + "HP:0011120" + ], + "boxer 's nasal deformity": [ + "HP:0011120" + ], + "boxer 's nose deformity": [ + "HP:0011120" + ], + "concave dorsum of nose": [ + "HP:0011120" + ], + "concave nasal dorsum": [ + "HP:0011120" + ], + "saddle nose": [ + "HP:0011120" + ], + "saddle nose deformity": [ + "HP:0011120" + ], + "saddle shape nasal dorsum": [ + "HP:0011120" + ], + "saddle shaped nasal dorsum": [ + "HP:0011120" + ], + "ski jump nose": [ + "HP:0011120" + ], + "abnormality of skin morphology": [ + "HP:0011121" + ], + "abnormal skin morphology": [ + "HP:0011121" + ], + "abnormal skin structure": [ + "HP:0011121" + ], + "abnormality of skin physiology": [ + "HP:0011122" + ], + "inflammatory abnormality of the skin": [ + "HP:0011123" + ], + "abnormal tendency to infection of the skin": [ + "HP:0011123" + ], + "abnormal tendency to infections of the skin": [ + "HP:0011123" + ], + "dermatitis": [ + "HP:0011123" + ], + "inflammatory skin disease": [ + "HP:0011123" + ], + "skin inflammation": [ + "HP:0011123" + ], + "abnormal epidermal morphology": [ + "HP:0011124" + ], 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"HP:0011133" + ], + "increase sensitivity to ionise radiation": [ + "HP:0011133" + ], + "increased sensitivity to ionising radiation": [ + "HP:0011133" + ], + "low - grade fever": [ + "HP:0011134" + ], + "mild fever": [ + "HP:0011134" + ], + "aplasia / hypoplasia of the sweat gland": [ + "HP:0011135" + ], + "aplasia / hypoplasia of the sweat glands": [ + "HP:0011135" + ], + "absent / small sweat gland": [ + "HP:0011135" + ], + "absent / small sweat glands": [ + "HP:0011135" + ], + "absent / underdevelop sweat gland": [ + "HP:0011135" + ], + "absent / underdeveloped sweat glands": [ + "HP:0011135" + ], + "aplasia of the sweat gland": [ + "HP:0011136" + ], + "aplasia of the sweat glands": [ + "HP:0011136" + ], + "absent sweat gland": [ + "HP:0011136" + ], + "absent sweat glands": [ + "HP:0011136" + ], + "lack of sweat gland": [ + "HP:0011136" + ], + "lack of sweat glands": [ + "HP:0011136" + ], + "non - pruritic urticaria": [ + "HP:0011137" + ], + "non - itchy hive": [ + "HP:0011137" + ], + "non - itchy hives": [ + "HP:0011137" + ], + "abnormality of skin adnexa morphology": [ + "HP:0011138" + ], + "abnormal skin appendage": [ + "HP:0011138" + ], + "gastric duplication": [ + "HP:0011139" + ], + "gastric duplication cyst": [ + "HP:0011139" + ], + "gastrointestinal duplication": [ + "HP:0011140" + ], + "gi duplication": [ + "HP:0011140" + ], + "age - relate cataract": [ + "HP:0011141" + ], + "age - related cataract": [ + "HP:0011141" + ], + "clouding of the lens of the eye with age": [ + "HP:0011141" + ], + "age - related nuclear cataract": [ + "HP:0011142" + ], + "age - related cortical cataract": [ + "HP:0011143" + ], + "age - related posterior subcapsular cataract": [ + "HP:0011144" + ], + "symptomatic seizure": [ + "HP:0011145" + ], + "symptomatic seizures": [ + "HP:0011145" + ], + "dialeptic seizure": [ + "HP:0011146" + ], + "behavioral arrest seizure with impairment of awareness irrespective of onset": [ + "HP:0011146" + ], + "behavioural arrest seizure with impairment of awareness irrespective of onset": [ + "HP:0011146" + ], + "unknown onset behavioral arrest seizure with impairment of awareness": [ + "HP:0011146" + ], + "unknown onset behavioural arrest seizure with impairment of awareness": [ + "HP:0011146" + ], + "typical absence seizure": [ + "HP:0011147" + ], + "typical absence": [ + "HP:0011147" + ], + "typical absence seizures": [ + "HP:0011147" + ], + "obsolete absence seizure with special feature": [ + "HP:0011148" + ], + "obsolete absence seizures with special features": [ + "HP:0011148" + ], + "absence seizure with eyelid myoclonia": [ + "HP:0011149" + ], + "absence seizures with eyelid myoclonia": [ + "HP:0011149" + ], + "myoclonic absence seizure": [ + "HP:0011150" + ], + "myoclonic absence": [ + "HP:0011150" + ], + "myoclonic absences": [ + "HP:0011150" + ], + "atypical absence status epilepticus": [ + "HP:0011151" + ], + "obtundation status": [ + "HP:0011151" + ], + "early onset absence seizure": [ + "HP:0011152" + ], + "early onset absence seizures": [ + "HP:0011152" + ], + "early onset petit mal seizure": [ + "HP:0011152" + ], + "early onset petit mal seizures": [ + "HP:0011152" + ], + "focal motor seizure": [ + "HP:0011153" + ], + "focal motor seizures": [ + "HP:0011153" + ], + "localise motor seizure": [ + "HP:0011153" + ], + "localised motor seizure": [ + "HP:0011153" + ], + "localised motor seizures": [ + "HP:0011153" + ], + "localize motor seizure": [ + "HP:0011153" + ], + "localized motor seizure": [ + "HP:0011153" + ], + "localized motor seizures": [ + "HP:0011153" + ], + "partial motor seizure": [ + "HP:0011153" + ], + "partial motor seizures": [ + "HP:0011153" + ], + "segmental motor seizure": [ + "HP:0011153" + ], + "focal autonomic seizure": [ + "HP:0011154" + ], + "focal autonomic seizures": [ + "HP:0011154" + ], + "obsolete focal autonomic seizure with altered responsiveness": [ + "HP:0011155" + ], + "obsolete focal autonomic seizures with altered responsiveness": [ + "HP:0011155" + ], + "obsolete focal autonomic seizure without altered responsiveness": [ + "HP:0011156" + ], + "obsolete focal autonomic seizures without altered responsiveness": [ + "HP:0011156" + ], + "focal sensory seizure": [ + "HP:0011157" + ], + "focal sensory seizures": [ + "HP:0011157" + ], + "partial sensory seizure": [ + "HP:0011157" + ], + "sensory aura": [ + "HP:0011157" + ], + "focal sensory seizure with auditory feature": [ + "HP:0011158" + ], + "focal sensory seizure with auditory features": [ + "HP:0011158" + ], + "auditory aura": [ + "HP:0011158" + ], + "focal auditory seizure": [ + "HP:0011158" + ], + "focal sensory auditory seizure": [ + "HP:0011158" + ], + "partial auditory seizure": [ + "HP:0011158" + ], + "focal autonomic seizure with epigastric sensation / nausea / vomiting / other gastrointestinal phenomenon": [ + "HP:0011159" + ], + "focal autonomic seizure with epigastric sensation / nausea / vomiting / other gastrointestinal phenomena": [ + "HP:0011159" + ], + "abdominal aura": [ + "HP:0011159" + ], + "epigastric aura": [ + "HP:0011159" + ], + "epigastric auras": [ + "HP:0011159" + ], + "localised seizure with epigastric sensation": [ + "HP:0011159" + ], + "localized seizure with epigastric sensation": [ + "HP:0011159" + ], + "partial seizure with epigastric sensation": [ + "HP:0011159" + ], + "visceral aura": [ + "HP:0011159" + ], + "focal sensory seizure with gustatory feature": [ + "HP:0011160" + ], + "focal sensory seizure with gustatory features": [ + "HP:0011160" + ], + "focal gustatory seizure": [ + "HP:0011160" + ], + "focal sensory gustatory seizure": [ + "HP:0011160" + ], + "gustatory aura": [ + "HP:0011160" + ], + "gustatory auras": [ + "HP:0011160" + ], + "partial gustatory seizure": [ + "HP:0011160" + ], + "taste hallucination": [ + "HP:0011160" + ], + "taste hallucinations": [ + "HP:0011160" + ], + "focal sensory seizure with olfactory feature": [ + "HP:0011161" + ], + "focal sensory seizure with olfactory features": [ + "HP:0011161" + ], 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partial occipital seizure": [ + "HP:0011165" + ], + "simple partial occipital seizures": [ + "HP:0011165" + ], + "visual aura": [ + "HP:0011165" + ], + "visual auras": [ + "HP:0011165" + ], + "focal myoclonic seizure": [ + "HP:0011166" + ], + "focal myoclonic seizures": [ + "HP:0011166" + ], + "local myoclonic seizure": [ + "HP:0011166" + ], + "local myoclonic seizures": [ + "HP:0011166" + ], + "localise myoclonic seizure": [ + "HP:0011166" + ], + "localised myoclonic seizure": [ + "HP:0011166" + ], + "localize myoclonic seizure": [ + "HP:0011166" + ], + "localized myoclonic seizure": [ + "HP:0011166" + ], + "partial myoclonic seizure": [ + "HP:0011166" + ], + "partial myoclonic seizures": [ + "HP:0011166" + ], + "segmental myoclonic seizure": [ + "HP:0011166" + ], + "segmental myoclonic seizures": [ + "HP:0011166" + ], + "focal tonic seizure": [ + "HP:0011167" + ], + "focal tonic seizures": [ + "HP:0011167" + ], + "local tonic seizure": [ + "HP:0011167" + ], + "local tonic seizures": [ + "HP:0011167" + ], + "localise tonic seizure": [ + "HP:0011167" + ], + "localised tonic seizure": [ + "HP:0011167" + ], + "localize tonic seizure": [ + "HP:0011167" + ], + "localized tonic seizure": [ + "HP:0011167" + ], + "partial tonic seizure": [ + "HP:0011167" + ], + "partial tonic seizures": [ + "HP:0011167" + ], + "segmental tonic seizure": [ + "HP:0011167" + ], + "focal seizure with eyelid myoclonia": [ + "HP:0011168" + ], + "eyelid myoclonias": [ + "HP:0011168" + ], + "generalize clonic seizure": [ + "HP:0011169" + ], + "generalized clonic seizure": [ + "HP:0011169" + ], + "generalise clonic seizure": [ + "HP:0011169" + ], + "generalised clonic seizure": [ + "HP:0011169" + ], + "generalised clonic seizures": [ + "HP:0011169" + ], + "generalise onset clonic seizure": [ + "HP:0011169" + ], + "generalised onset clonic seizure": [ + "HP:0011169" + ], + "generalise - onset clonic seizure": [ + "HP:0011169" + ], + "generalised - onset clonic seizure": [ + "HP:0011169" + ], + "generalized clonic seizures": [ + "HP:0011169" + ], + "generalize onset clonic seizure": [ + "HP:0011169" + ], + "generalized onset clonic seizure": [ + "HP:0011169" + ], + "generalize - onset clonic seizure": [ + "HP:0011169" + ], + "generalized - onset clonic seizure": [ + "HP:0011169" + ], + "generalize myoclonic - atonic seizure": [ + "HP:0011170" + ], + "generalized myoclonic - atonic seizure": [ + "HP:0011170" + ], + "generalise myoclonic - atonic seizure": [ + "HP:0011170" + ], + "generalised myoclonic - atonic seizure": [ + "HP:0011170" + ], + "myoclonic atonic seizure": [ + "HP:0011170" + ], + "myoclonic atonic seizures": [ + "HP:0011170" + ], + "myoclonic - astatic seizure": [ + "HP:0011170" + ], + "simple febrile seizure": [ + "HP:0011171" + ], + "simple febrile convulsion": [ + "HP:0011171" + ], + "simple febrile seizures": [ + "HP:0011171" + ], + "simple fever fit": [ + "HP:0011171" + ], + "complex febrile seizure": [ + "HP:0011172" + ], + "complex febrile convulsion": [ 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seizure": [ + "HP:0011174" + ], + "localized hyperkinetic seizure": [ + "HP:0011174" + ], + "partial hyperkinetic seizure": [ + "HP:0011174" + ], + "segmental hyperkinetic seizure": [ + "HP:0011174" + ], + "focal motor seizure with version": [ + "HP:0011175" + ], + "versive seizure": [ + "HP:0011175" + ], + "versive seizures": [ + "HP:0011175" + ], + "eeg with constitutional variant": [ + "HP:0011176" + ], + "eeg with constitutional variants": [ + "HP:0011176" + ], + "eeg with 4 - 5 / second background activity": [ + "HP:0011177" + ], + "alpha - eeg": [ + "HP:0011178" + ], + "beta - eeg": [ + "HP:0011179" + ], + "beta wave electroencephalography": [ + "HP:0011179" + ], + "partial beta - eeg": [ + "HP:0011180" + ], + "low voltage eeg": [ + "HP:0011181" + ], + "interictal epileptiform activity": [ + "HP:0011182" + ], + "epileptiform eeg discharge": [ + "HP:0011182" + ], + "epileptiform eeg discharges": [ + "HP:0011182" + ], + "eeg with hyperventilation - induced focal epileptiform discharge": [ + "HP:0011183" + ], + "eeg with hyperventilation - induced focal epileptiform discharges": [ + "HP:0011183" + ], + "eeg with hyperventilation - induced generalized epileptiform discharge": [ + "HP:0011184" + ], + "eeg with hyperventilation - induced generalized epileptiform discharges": [ + "HP:0011184" + ], + "eeg with hyperventilation - induce generalised epileptiform discharge": [ + "HP:0011184" + ], + "eeg with hyperventilation - induced generalised epileptiform discharges": [ + "HP:0011184" + ], + "eeg with focal epileptiform discharge": [ + "HP:0011185" + ], + "eeg with focal epileptiform discharges": [ + "HP:0011185" + ], + "focal eeg abnormality": [ + "HP:0011185" + ], + "focal epileptiform discharge with limited propagation to contralateral hemisphere": [ + "HP:0011186" + ], + "focal epileptiform discharges with limited propagation to contralateral hemisphere": [ + "HP:0011186" + ], + "focal eeg discharge with propagation to ipsilateral hemisphere": [ + "HP:0011187" + ], + "focal eeg discharges with propagation to ipsilateral hemisphere": [ + "HP:0011187" + ], + "focal eeg discharge with secondary generalization": [ + "HP:0011188" + ], + "focal eeg discharges with secondary generalization": [ + "HP:0011188" + ], + "focal eeg discharge with secondary generalisation": [ + "HP:0011188" + ], + "focal eeg discharges with secondary generalisation": [ + "HP:0011188" + ], + "bilateral multifocal epileptiform discharge": [ + "HP:0011189" + ], + "bilateral multifocal epileptiform discharges": [ + "HP:0011189" + ], + "uni - and bilateral multifocal epileptiform discharge": [ + "HP:0011190" + ], + "uni - and bilateral multifocal epileptiform discharges": [ + "HP:0011190" + ], + "unilateral multifocal epileptiform discharge": [ + "HP:0011191" + ], + "unilateral multifocal epileptiform discharges": [ + "HP:0011191" + ], + "polymorphic focal epileptiform discharge": [ + "HP:0011192" + ], + "polymorphic focal epileptiform discharges": [ + "HP:0011192" + ], + "eeg with focal spike": [ + "HP:0011193" + ], + "eeg with focal spikes": [ + "HP:0011193" + ], + "eeg with series of focal spike": [ + "HP:0011194" + ], + "eeg with series of focal spikes": [ + "HP:0011194" + ], + "eeg with focal sharp slow wave": [ + "HP:0011195" + ], + "eeg with focal sharp slow waves": [ + "HP:0011195" + ], + "eeg with focal sharp wave": [ + "HP:0011196" + ], + "eeg with focal sharp waves": [ + "HP:0011196" + ], + "eeg with focal spike wave": [ + "HP:0011197" + ], + "eeg with focal spike waves": [ + "HP:0011197" + ], + "eeg with generalized epileptiform discharge": [ + "HP:0011198" + ], + "eeg with generalized epileptiform discharges": [ + "HP:0011198" + ], + "eeg with generalised epileptiform discharge": [ + "HP:0011198" + ], + "eeg with generalised epileptiform discharges": [ + "HP:0011198" + ], + "eeg with generalized sharp slow wave": [ + "HP:0011199" + ], + "eeg with generalized sharp slow waves": [ + "HP:0011199" + ], + "eeg with generalised sharp slow wave": [ + "HP:0011199" + ], + "eeg with generalised sharp slow waves": [ + "HP:0011199" + ], + "eeg with generalized polymorphic epileptiform discharge": [ + "HP:0011200" + ], + "eeg with generalized polymorphic epileptiform discharges": [ + "HP:0011200" + ], + "eeg with generalised polymorphic epileptiform discharge": [ + "HP:0011200" + ], + "eeg with generalised polymorphic epileptiform discharges": [ + "HP:0011200" + ], + "eeg with change in voltage": [ + "HP:0011201" + ], + "eeg with changes in voltage": [ + "HP:0011201" + ], + "eeg with diffuse acceleration": [ + "HP:0011202" + ], + "eeg with abnormally slow frequency": [ + "HP:0011203" + ], + "eeg with abnormally slow frequencies": [ + "HP:0011203" + ], + "eeg with continuous slow activity": [ + "HP:0011204" + ], + "eeg with intermittent slow activity": [ + "HP:0011205" + ], + "eeg with generalized slow activity grade 1": [ + "HP:0011206" + ], + "eeg with generalised slow activity grade 1": [ + "HP:0011206" + ], + "eeg with generalized slow activity grade 2": [ + "HP:0011207" + ], + "eeg with generalised slow activity grade 2": [ + "HP:0011207" + ], + "eeg with generalized slow activity grade 3": [ + "HP:0011208" + ], + "eeg with generalised slow activity grade 3": [ + "HP:0011208" + ], + "eeg with generalized slow activity grade 4": [ + "HP:0011209" + ], + "eeg with generalised slow activity grade 4": [ + "HP:0011209" + ], + "flat line eeg": [ + "HP:0011209" + ], + "eeg with occipital slow": [ + "HP:0011210" + ], + "eeg with occipital slowing": [ + "HP:0011210" + ], + "eeg with photoparoxysmal response grade i": [ + "HP:0011211" + ], + "eeg with photoparoxysmal response grade ii": [ + "HP:0011212" + ], + "eeg with photoparoxysmal response grade iii": [ + "HP:0011213" + ], + "eeg with photoparoxysmal response grade iv": [ + "HP:0011214" + ], + "hemihypsarrhythmia": [ + "HP:0011215" + ], + "abnormal shape of the occiput": [ + "HP:0011217" + ], + "abnormal shape of posterior cranium": [ + "HP:0011217" + ], + "abnormal shape of posterior head": [ + "HP:0011217" + ], + "abnormal shape of posterior skull": [ + "HP:0011217" + ], + "abnormal shape of the back of the head": [ + "HP:0011217" + ], + "abnormal shape of the back of the skull": [ + "HP:0011217" + ], + "abnormal shape of the frontal region": [ + "HP:0011218" + ], + "abnormal morphology of the frontal region": [ + "HP:0011218" + ], + "abnormal shape of the forehead": [ + "HP:0011218" + ], + "dysmorphic forehead": [ + "HP:0011218" + ], + "dysmorphic frontal region": [ + "HP:0011218" + ], + "short face": [ + "HP:0011219" + ], + "decreased height of face": [ + "HP:0011219" + ], + "decreased length of face": [ + "HP:0011219" + ], + "decreased vertical dimension of face": [ + "HP:0011219" + ], + "short facies": [ + "HP:0011219" + ], + "vertical deficiency of face": [ + "HP:0011219" + ], + "vertical facial deficiency": [ + "HP:0011219" + ], + "vertical facial insufficiency": [ + "HP:0011219" + ], + "vertical hypoplasia of face": [ + "HP:0011219" + ], + "vertical insufficiency of face": [ + "HP:0011219" + ], + "vertical shortening of face": [ + "HP:0011219" + ], + "prominent forehead": [ + "HP:0011220" + ], + "bulge forehead": [ + "HP:0011220" + ], + "bulging forehead": [ + "HP:0011220" + ], + "prominence of frontal region": [ + "HP:0011220" + ], + "pronounce forehead": [ + "HP:0011220" + ], + "pronounced forehead": [ + "HP:0011220" + ], + "protrude forehead": [ + "HP:0011220" + ], + "protruding forehead": [ + "HP:0011220" + ], + "vertical forehead crease": [ + "HP:0011221" + ], + "vertical forehead creases": [ + "HP:0011221" + ], + "frontal crease of face": [ + "HP:0011221" + ], + "frontal creases of face": [ + "HP:0011221" + ], + "vertical forehead rhytids": [ + "HP:0011221" + ], + "vertical forehead wrinkle": [ + "HP:0011221" + ], + "vertical forehead wrinkles": [ + "HP:0011221" + ], + "depressed glabella": [ + "HP:0011222" + ], + "concave glabella": [ + "HP:0011222" + ], + "deficiency of glabella": [ + "HP:0011222" + ], + "deficient area between the eyebrow": [ + "HP:0011222" + ], + "deficient area between the eyebrows": [ + "HP:0011222" + ], + "flat area between the eyebrow": [ + "HP:0011222" + ], + "flat area between the eyebrows": [ + "HP:0011222" + ], + "flat glabella": [ + "HP:0011222" + ], + "hypoplasia of glabella": [ + "HP:0011222" + ], + "metopic depression": [ + "HP:0011223" + ], + "depression of frontal cranial suture": [ + "HP:0011223" + ], + "depression of metopic cranial suture": [ + "HP:0011223" + ], + "frontal suture depression": [ + "HP:0011223" + ], + "ablepharon": [ + "HP:0011224" + ], + "ablepharon of eyelid": [ + "HP:0011224" + ], + "absent eyelid": [ + "HP:0011224" + ], + "absent eyelids": [ + "HP:0011224" + ], + "agenesis of eyelid": [ + "HP:0011224" + ], + "agenesis of eyelids": [ + "HP:0011224" + ], + "aplasia of the eyelid": [ + "HP:0011224" + ], + "aplasia of the eyelids": [ + "HP:0011224" + ], + "miss eyelid": [ + "HP:0011224" + ], + "missing eyelids": [ + "HP:0011224" + ], + "epiblepharon": [ + "HP:0011225" + ], + "aplasia / hypoplasia of the eyelid": [ + "HP:0011226" + ], + "failure of development of eyelid": [ + "HP:0011226" + ], + "hypotrophic eyelid": [ + "HP:0011226" + ], + "elevate circulate c - reactive protein concentration": [ + "HP:0011227" + ], + "elevated circulating c - reactive protein concentration": [ + "HP:0011227" + ], + "elevate c - reactive protein level": [ + "HP:0011227" + ], + "elevated c - reactive protein level": [ + "HP:0011227" + ], + "elevate crp": [ + "HP:0011227" + ], + "elevated crp": [ + "HP:0011227" + ], + "horizontal eyebrow": [ + "HP:0011228" + ], + "flat eyebrow": [ + "HP:0011228" + ], + "lack of eyebrow arch": [ + "HP:0011228" + ], + "lack of eyebrow curvature": [ + "HP:0011228" + ], + "straight eyebrow": [ + "HP:0011228" + ], + "straight eyebrows": [ + "HP:0011228" + ], + "broad eyebrow": [ + "HP:0011229" + ], + "broad eyebrows": [ + "HP:0011229" + ], + "flare eyebrow": [ + "HP:0011229" + ], + "flared eyebrow": [ + "HP:0011229" + ], + "flared eyebrows": [ + "HP:0011229" + ], + "increased vertical height of eyebrow": [ + "HP:0011229" + ], + "increased vertical thickness of eyebrow": [ + "HP:0011229" + ], + "increased vertical width of eyebrow": [ + "HP:0011229" + ], + "laterally extend eyebrow": [ + "HP:0011230" + ], + "laterally extended eyebrow": [ + "HP:0011230" + ], + "increase lateral length of eyebrow": [ + "HP:0011230" + ], + "increased lateral length of eyebrow": [ + "HP:0011230" + ], + "laterally elongate eyebrow": [ + "HP:0011230" + ], + "laterally elongated eyebrow": [ + "HP:0011230" + ], + "laterally extended eyebrows": [ + "HP:0011230" + ], + "prominent eyelash": [ + "HP:0011231" + ], + "prominent eyelashes": [ + "HP:0011231" + ], + "thick eyelash": [ + "HP:0011231" + ], + "thick eyelashes": [ + "HP:0011231" + ], + "infra - orbital fold": [ + "HP:0011232" + ], + "dennie - morgan fold": [ + "HP:0011232" + ], + "infraorbital fold": [ + "HP:0011232" + ], + "antihelical shelf": [ + "HP:0011233" + ], + "conchal shelf": [ + "HP:0011233" + ], + "absent antihelix": [ + "HP:0011234" + ], + "additional crus of antihelix": [ + "HP:0011235" + ], + "angulate antihelix": [ + "HP:0011236" + ], + "angulated antihelix": [ + "HP:0011236" + ], + "broad inferior crus of antihelix": [ + "HP:0011237" + ], + "antihelix , inferior crus , broad": [ + "HP:0011237" + ], + "prominent inferior crus of antihelix": [ + "HP:0011238" + ], + "antihelix , inferior crus , prominent": [ + "HP:0011238" + ], + "hyperplastic inferior crus of antihelix": [ + "HP:0011238" + ], + "hypertrophic inferior crus of antihelix": [ + "HP:0011238" + ], + "underdeveloped inferior crus of antihelix": [ + "HP:0011239" + ], + "antihelix , inferior crus , underdevelop": [ + "HP:0011239" + ], + "antihelix , inferior crus , underdeveloped": [ + "HP:0011239" + ], + "hypoplastic inferior crus of antihelix": [ + "HP:0011239" + ], + "hypotrophic inferior crus of antihelix": [ + "HP:0011239" + ], + "prominent stem of antihelix": [ + "HP:0011240" + ], + "hyperplastic antihelix stem": [ + "HP:0011240" + ], + "hypertrophic antihelix stem": [ + "HP:0011240" + ], + "serpiginous stem of antihelix": [ + "HP:0011241" + ], + "antihelix , stem , serpiginous": [ + "HP:0011241" + ], + "underdeveloped stem of antihelix": [ + "HP:0011242" + ], + "antihelix , stem , underdevelop": [ + "HP:0011242" + ], + "antihelix , stem , underdeveloped": [ + "HP:0011242" + ], + "abnormality of inferior crus of antihelix": [ + "HP:0011243" + ], + "abnormality of anterior crus of antihelix": [ + "HP:0011243" + ], + "abnormality of stem of antihelix": [ + "HP:0011244" + ], + "abnormality of superior crus of antihelix": [ + "HP:0011245" + ], + "abnormality of posterior crus of antihelix": [ + "HP:0011245" + ], + "underdeveloped superior crus of antihelix": [ + "HP:0011246" + ], + "hypoplastic superior crus of antihelix": [ + "HP:0011246" + ], + "hypotrophic superior crus of antihelix": [ + "HP:0011246" + ], + "prominent superior crus of antihelix": [ + "HP:0011247" + ], + "hyperplastic superior crus of antihelix": [ + "HP:0011247" + ], + "hypertrophic superior crus of antihelix": [ + "HP:0011247" + ], + "evert antitragus": [ + "HP:0011248" + ], + "everted antitragus": [ + "HP:0011248" + ], + "absent antitragus": [ + "HP:0011249" + ], + "bifid antitragus": [ + "HP:0011250" + ], + "double antitragus": [ + "HP:0011250" + ], + "underdeveloped antitragus": [ + "HP:0011251" + ], + "hypoplastic antitragus": [ + "HP:0011251" + ], + "hypotrophic antitragus": [ + "HP:0011251" + ], + "small antitragus": [ + "HP:0011251" + ], + "cryptotia": [ + "HP:0011252" + ], + "bury ear": [ + "HP:0011252" + ], + "buried ear": [ + "HP:0011252" + ], + "hidden ear": [ + "HP:0011252" + ], + "type i cryptotia": [ + "HP:0011253" + ], + "type 1 cryptotia": [ + "HP:0011253" + ], + "type ii cryptotia": [ + "HP:0011254" + ], + "type 2 cryptotia": [ + "HP:0011254" + ], + "absent crus of helix": [ + "HP:0011255" + ], + "helix , crus , absent": [ + "HP:0011255" + ], + "crus of helix connect to antihelix": [ + "HP:0011256" + ], + "crus of helix connected to antihelix": [ + "HP:0011256" + ], + "helix , crus , connect to antihelix": [ + "HP:0011256" + ], + "helix , crus , connected to antihelix": [ + "HP:0011256" + ], + "serpiginous crus of helix": [ + "HP:0011257" + ], + "helix , crus , serpiginous": [ + "HP:0011257" + ], + "tragal bridge of crus of helix": [ + "HP:0011258" + ], + "helix , crus , tragal bridge": [ + "HP:0011258" + ], + "expand terminal portion of crus of helix": [ + "HP:0011259" + ], + "expanded terminal portion of crus of helix": [ + "HP:0011259" + ], + "helix , crus , expand terminal portion": [ + "HP:0011259" + ], + "helix , crus , expanded terminal portion": [ + "HP:0011259" + ], + "darwin notch of helix": [ + "HP:0011260" + ], + "helix , darwin notch": [ + "HP:0011260" + ], + "darwin tubercle of helix": [ + "HP:0011261" + ], + "helix , darwin tubercle": [ + "HP:0011261" + ], + "crimped helix": [ + "HP:0011262" + ], + "helix , crimp": [ + "HP:0011262" + ], + "helix , crimped": [ + "HP:0011262" + ], + "indent helix": [ + "HP:0011262" + ], + "indented helix": [ + "HP:0011262" + ], + "forward face earlobe": [ + "HP:0011263" + ], + "forward facing earlobe": [ + "HP:0011263" + ], + "lobe , forward face": [ + "HP:0011263" + ], + "lobe , forward facing": [ + "HP:0011263" + ], + "discontinuous ascend root of helix": [ + "HP:0011264" + ], + "discontinuous ascending root of helix": [ + "HP:0011264" + ], + "helix , discontinuous ascend root": [ + "HP:0011264" + ], + "helix , discontinuous ascending root": [ + "HP:0011264" + ], + "cleft earlobe": [ + "HP:0011265" + ], + "microtia , first degree": [ + "HP:0011266" + ], + "first - degree microtia": [ + "HP:0011266" + ], + "microtia , third degree": [ + "HP:0011267" + ], + "abnormal shape / structure of ear": [ + "HP:0011267" + ], + "third - degree microtia": [ + "HP:0011267" + ], + "absent tragus": [ + "HP:0011268" + ], + "bifid tragus": [ + "HP:0011269" + ], + "notch tragus": [ + "HP:0011269" + ], + "notched tragus": [ + "HP:0011269" + ], + "tragus , bifid": [ + "HP:0011269" + ], + "duplicate tragus": [ + "HP:0011270" + ], + "duplicated tragus": [ + "HP:0011270" + ], + "accesory tragus": [ + "HP:0011270" + ], + "tragus , duplicate": [ + "HP:0011270" + ], + "tragus , duplicated": [ + "HP:0011270" + ], + "prominent tragus": [ + "HP:0011271" + ], + "enlarge tragus": [ + "HP:0011271" + ], + "enlarged tragus": [ + "HP:0011271" + ], + "hyperplastic tragus": [ + "HP:0011271" + ], + "hypertrophic tragus": [ + "HP:0011271" + ], + "large tragus": [ + "HP:0011271" + ], + "tragus , prominent": [ + "HP:0011271" + ], + "underdeveloped tragus": [ + "HP:0011272" + ], + "hypoplastic tragus": [ + "HP:0011272" + ], + "hypotrophic tragus": [ + "HP:0011272" + ], + "small tragus": [ + "HP:0011272" + ], + "anisocytosis": [ + "HP:0011273" + ], + "unequal size of red blood cell": [ + "HP:0011273" + ], + "unequal size of red blood cells": [ + "HP:0011273" + ], + "recurrent mycobacterial infection": [ + "HP:0011274" + ], + "recurrent mycobacterial infections": [ + "HP:0011274" + ], + "recurrent mycobacterium avium complex infection": [ + "HP:0011275" + ], + "recurrent mycobacterium avium complex infections": [ + "HP:0011275" + ], + "vascular skin abnormality": [ + "HP:0011276" + ], + "skin vascular malformation": [ + "HP:0011276" + ], + "vascular abnormality restrict to skin": [ + "HP:0011276" + ], + "vascular abnormalities restricted to skin": [ + "HP:0011276" + ], + "abnormality of the urinary system physiology": [ + "HP:0011277" + ], + "intrapulmonary sequestration": [ + "HP:0011278" + ], + "abnormality of urine bicarbonate concentration": [ + "HP:0011279" + ], + "abnormality of urine hco3 concentration": [ + "HP:0011279" + ], + "abnormality of urine calcium concentration": [ + "HP:0011280" + ], + "abnormality of urine ca concentration": [ + "HP:0011280" + ], + "abnormality of urine ca2+ concentration": [ + "HP:0011280" + ], + "abnormality of urine catecholamine concentration": [ + "HP:0011281" + ], + "abnormality of hindbrain morphology": [ + "HP:0011282" + ], + "abnormal shape of hindbrain": [ + "HP:0011282" + ], + "abnormality of the hindbrain": [ + "HP:0011282" + ], + "abnormal metencephalon morphology": [ + "HP:0011283" + ], + "abnormality of the metencephalon": [ + "HP:0011283" + ], + "short - segment aganglionic megacolon": [ + "HP:0011284" + ], + "long - segment aganglionic megacolon": [ + "HP:0011285" + ], + "total colonic aganglionosis": [ + "HP:0011286" + ], + "eeg with occipital sharp slow wave": [ + "HP:0011287" + ], + "eeg with occipital sharp slow waves": [ + "HP:0011287" + ], + "eeg with parietal sharp slow wave": [ + "HP:0011288" + ], + "eeg with parietal sharp slow waves": [ + "HP:0011288" + ], + "eeg with temporal sharp slow wave": [ + "HP:0011289" + ], + "eeg with temporal sharp slow waves": [ + "HP:0011289" + ], + "eeg with frontal sharp slow wave": [ + "HP:0011290" + ], + "eeg with frontal sharp slow waves": [ + "HP:0011290" + ], + "eeg with central sharp slow wave": [ + "HP:0011291" + ], + "eeg with central sharp slow waves": [ + "HP:0011291" + ], + "eeg with occipital sharp wave": [ + "HP:0011292" + ], + "eeg with occipital sharp waves": [ + "HP:0011292" + ], + "eeg with central sharp wave": [ + "HP:0011293" + ], + "eeg with central sharp waves": [ + "HP:0011293" + ], + "eeg with frontal sharp wave": [ + "HP:0011294" + ], + "eeg with frontal sharp waves": [ + "HP:0011294" + ], + "eeg with parietal sharp wave": [ + "HP:0011295" + ], + "eeg with parietal sharp waves": [ + "HP:0011295" + ], + "eeg with temporal sharp wave": [ + "HP:0011296" + ], + "eeg with temporal sharp waves": [ + "HP:0011296" + ], + "abnormal digit morphology": [ + "HP:0011297" + ], + "abnormality of digit": [ + "HP:0011297" + ], + "abnormality of finger or toe": [ + "HP:0011297" + ], + "abnormality of fingers or toes": [ + "HP:0011297" + ], + "digital anomaly": [ + "HP:0011297" + ], + "digital anomalies": [ + "HP:0011297" + ], + "prominent digit pad": [ + "HP:0011298" + ], + "partial absence of finger": [ + "HP:0011299" + ], + "broad fingertip": [ + "HP:0011300" + ], + "broad fingertips": [ + "HP:0011300" + ], + "absent foot": [ + "HP:0011301" + ], + "aplasia of the foot": [ + "HP:0011301" + ], + "apodia": [ + "HP:0011301" + ], + "long palm": [ + "HP:0011302" + ], + "convex contour of sole": [ + "HP:0011303" + ], + "broad thumb": [ + "HP:0011304" + ], + "broad phalanx of the thumb": [ + "HP:0011304" + ], + "broad phalanges of the thumb": [ + "HP:0011304" + ], + "broad thumbs": [ + "HP:0011304" + ], + "wide / broad thumb": [ + "HP:0011304" + ], + "wide / broad thumb phalanx": [ + "HP:0011304" + ], + "wide / broad thumb phalanges": [ + "HP:0011304" + ], + "partial absence of toe": [ + "HP:0011305" + ], + "hypophalangy of toe": [ + "HP:0011305" + ], + "hypophalangy of toes": [ + "HP:0011305" + ], + "splay toe": [ + "HP:0011307" + ], + "splayed toes": [ + "HP:0011307" + ], + "slender toe": [ + "HP:0011308" + ], + "narrow toe": [ + "HP:0011308" + ], + "taper toe": [ + "HP:0011309" + ], + "tapered toe": [ + "HP:0011309" + ], + "tapering toe": [ + "HP:0011309" + ], + "tapering toes": [ + "HP:0011309" + ], + "bridge palmar crease": [ + "HP:0011310" + ], + "bridged palmar crease": [ + "HP:0011310" + ], + "bridge palm line": [ + "HP:0011310" + ], + "bridged palm line": [ + "HP:0011310" + ], + "transitional palmar crease": [ + "HP:0011310" + ], + "sydney crease": [ + "HP:0011311" + ], + "fuse nail": [ + "HP:0011312" + ], + "fused nails": [ + "HP:0011312" + ], + "narrow nail": [ + "HP:0011313" + ], + "abnormality of long bone morphology": [ + "HP:0011314" + ], + "abnormal shape of long bone": [ + "HP:0011314" + ], + "abnormality of the tubular bone": [ + "HP:0011314" + ], + "abnormality of the tubular bones": [ + "HP:0011314" + ], + "unicoronal synostosis": [ + "HP:0011315" + ], + "unilateral coronal craniosynostosis": [ + "HP:0011315" + ], + "unilateral coronal suture craniosynostosis": [ + "HP:0011315" + ], + "unilateral coronal suture synostosis": [ + "HP:0011315" + ], + "leave unicoronal synostosis": [ + "HP:0011316" + ], + "left unicoronal synostosis": [ + "HP:0011316" + ], + "right unicoronal synostosis": [ + "HP:0011317" + ], + "bicoronal synostosis": [ + "HP:0011318" + ], + "bilateral coronal craniosynostosis": [ + "HP:0011318" + ], + "bilateral coronal suture craniosynostosis": [ + "HP:0011318" + ], + "bilateral coronal suture synostosis": [ + "HP:0011318" + ], + "bilambdoid synostosis": [ + "HP:0011319" + ], + "bilateral lambdoid craniosynostosis": [ + "HP:0011319" + ], + "bilateral lambdoid suture synostosis": [ + "HP:0011319" + ], + "unilambdoid synostosis": [ + "HP:0011320" + ], + "unilateral lambdoid craniosynostosis": [ + "HP:0011320" + ], + "unilateral lambdoid suture synostosis": [ + "HP:0011320" + ], + "leave unilambdoid synostosis": [ + "HP:0011321" + ], + "left unilambdoid synostosis": [ + "HP:0011321" + ], + "right unilambdoid synostosis": [ + "HP:0011322" + ], + "cleft of chin": [ + "HP:0011323" + ], + "midline defect of chin": [ + "HP:0011323" + ], + "multiple suture craniosynostosis": [ + "HP:0011324" + ], + "multisutural craniosynostosis": [ + "HP:0011324" + ], + "pansynostosis": [ + "HP:0011325" + ], + "sysnostosis of all cranial suture": [ + "HP:0011325" + ], + "sysnostosis of all cranial sutures": [ + "HP:0011325" + ], + "anterior plagiocephaly": [ + "HP:0011326" + ], + "anterior flat head syndrome": [ + "HP:0011326" + ], + "coronal synostosis": [ + "HP:0011326" + ], + "deformational anterior plagiocephaly": [ + "HP:0011326" + ], + "deformational frontal plagiocephaly": [ + "HP:0011326" + ], + "frontal plagiocephaly": [ + "HP:0011326" + ], + "positional anterior plagiocephaly": [ + "HP:0011326" + ], + "positional frontal plagiocephaly": [ + "HP:0011326" + ], + "unicoronal craniosynostosis": [ + "HP:0011326" + ], + "posterior plagiocephaly": [ + "HP:0011327" + ], + "deformational posterior plagiocephaly": [ + "HP:0011327" + ], + "occipital plagiocephaly": [ + "HP:0011327" + ], + "abnormality of fontanelle": [ + "HP:0011328" + ], + "abnormality of fontanelles": [ + "HP:0011328" + ], + "anomaly of the fontanelle": [ + "HP:0011328" + ], + "anomaly of the fontanelles": [ + "HP:0011328" + ], + "abnormality of cranial suture": [ + "HP:0011329" + ], + "abnormality of cranial sutures": [ + "HP:0011329" + ], + "abnormality of the bregma suture": [ + "HP:0011329" + ], + "abnormality of the bregma sutures": [ + "HP:0011329" + ], + "abnormality of the calvarium suture": [ + "HP:0011329" + ], + "abnormality of the calvarium sutures": [ + "HP:0011329" + ], + "abnormality of the cranial suture": [ + "HP:0011329" + ], + "abnormality of the cranial sutures": [ + "HP:0011329" + ], + "abnormality of the skull suture": [ + "HP:0011329" + ], + "metopic synostosis": [ + "HP:0011330" + ], + "metopic craniosynostosis": [ + "HP:0011330" + ], + "metopic suture craniosynostosis": [ + "HP:0011330" + ], + "hemifacial atrophy": [ + "HP:0011331" + ], + "atrophy of half of face": [ + "HP:0011331" + ], + "atrophy of one side of the face": [ + "HP:0011331" + ], + "facial hemiatrophy": [ + "HP:0011331" + ], + "hemifacial hypoplasia": [ + "HP:0011332" + ], + "decrease in size of half of face": [ + "HP:0011332" + ], + "decrease in size of one side of the face": [ + "HP:0011332" + ], + "decreased size of half of the face": [ + "HP:0011332" + ], + "decreased size of one side of the face": [ + "HP:0011332" + ], + "hemifacial microsomia": [ + "HP:0011332" + ], + "shrinking of half of face": [ + "HP:0011332" + ], + "shrinking of one side of the face": [ + "HP:0011332" + ], + "asymmetric cry face": [ + "HP:0011333" + ], + "asymmetric crying face": [ + "HP:0011333" + ], + "hypoplasia of depressor angula oris muscle": [ + "HP:0011333" + ], + "partial unilateral facial paresis": [ + "HP:0011333" + ], + "facial shape deformation": [ + "HP:0011334" + ], + "distortion of facial shape": [ + "HP:0011334" + ], + "facial shape compression": [ + "HP:0011334" + ], + "frontal hirsutism": [ + "HP:0011335" + ], + "hairy forehead": [ + "HP:0011335" + ], + "hirsute forehead": [ + "HP:0011335" + ], + "bitemporal forceps mark": [ + "HP:0011336" + ], + "bitemporal forceps marks": [ + "HP:0011336" + ], + "bitemporal aplasia cutis congenita": [ + "HP:0011336" + ], + "congenital ectodermal dysplasia of the face": [ + "HP:0011336" + ], + "congenital , bilateral , scarlike facial lesion": [ + "HP:0011336" + ], + "congenital , bilateral , scarlike facial lesions": [ + "HP:0011336" + ], + "focal facial dermal dysplasia": [ + "HP:0011336" + ], + "temporal skin defect": [ + "HP:0011336" + ], + "abnormality of mouth size": [ + "HP:0011337" + ], + "anomaly of mouth size": [ + "HP:0011337" + ], + "abnormality of mouth shape": [ + "HP:0011338" + ], + "anomaly of mouth shape": [ + "HP:0011338" + ], + "unusual mouth shape": [ + "HP:0011338" + ], + "abnormality of upper lip vermillion": [ + "HP:0011339" + ], + "abnormality of the red part of the upper lip": [ + "HP:0011339" + ], + "anomaly of the upper lip vermillion": [ + "HP:0011339" + ], + "deformity of the upper lip vermillion": [ + "HP:0011339" + ], + "malformation of the upper lip vermillion": [ + "HP:0011339" + ], + "incomplete cleft of the upper lip": [ + "HP:0011340" + ], + "forme fruste unilateral cleft lip": [ + "HP:0011340" + ], + "incomplete cheiloschisis": [ + "HP:0011340" + ], + "notched cleft of the upper lip": [ + "HP:0011340" + ], + "partial cleft of the upper lip": [ + "HP:0011340" + ], + "long upper lip": [ + "HP:0011341" + ], + "elongation of upper lip": [ + "HP:0011341" + ], + "increase height of upper lip": [ + "HP:0011341" + ], + "increased height of upper lip": [ + "HP:0011341" + ], + "increased vertical length of upper lip": [ + "HP:0011341" + ], + "mild global developmental delay": [ + "HP:0011342" + ], + "global developmental delay , mild": [ + "HP:0011342" + ], + "psychomotor retardation , mild": [ + "HP:0011342" + ], + "moderate global developmental delay": [ + "HP:0011343" + ], + "global developmental delay , moderate": [ + "HP:0011343" + ], + "psychomotor retardation , moderate": [ + "HP:0011343" + ], + "severe global developmental delay": [ + "HP:0011344" + ], + "global developmental delay , severe": [ + "HP:0011344" + ], + "severe psychomotor retardation": [ + "HP:0011344" + ], + "moderate expressive language delay": [ + "HP:0011345" + ], + "mild expressive language delay": [ + "HP:0011346" + ], + "abnormality of ocular abduction": [ + "HP:0011347" + ], + "abnormal sixth cranial nerve morphology": [ + "HP:0011348" + ], + "abnormal abducens nerve morphology": [ + "HP:0011348" + ], + "abnormality of the sixth cranial nerve": [ + "HP:0011348" + ], + "obsolete abducens palsy": [ + "HP:0011349" + ], + "mild receptive language delay": [ + "HP:0011350" + ], + "moderate receptive language delay": [ + "HP:0011351" + ], + "severe receptive language delay": [ + "HP:0011352" + ], + "arterial intimal fibrosis": [ + "HP:0011353" + ], + "intimal fibrosis": [ + "HP:0011353" + ], + "generalize abnormality of skin": [ + "HP:0011354" + ], + "generalized abnormality of skin": [ + "HP:0011354" + ], + "generalised abnormality of skin": [ + "HP:0011354" + ], + "localize skin lesion": [ + "HP:0011355" + ], + "localized skin lesion": [ + "HP:0011355" + ], + "localise skin lesion": [ + "HP:0011355" + ], + "localised skin lesion": [ + "HP:0011355" + ], + "regional abnormality of skin": [ + "HP:0011356" + ], + "obsolete abnormality of hair density": [ + "HP:0011357" + ], + "generalize hypopigmentation of hair": [ + "HP:0011358" + ], + "generalized hypopigmentation of hair": [ + "HP:0011358" + ], + "generalised hypopigmentation of hair": [ + "HP:0011358" + ], + "dry hair": [ + "HP:0011359" + ], + "acquire abnormal hair pattern": [ + "HP:0011360" + ], + "acquired abnormal hair pattern": [ + "HP:0011360" + ], + "congenital abnormal 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"caesarian section": [ + "HP:0011410" + ], + "forceps delivery": [ + "HP:0011411" + ], + "ventouse delivery": [ + "HP:0011412" + ], + "vacuum extraction": [ + "HP:0011412" + ], + "vacuum - assist vaginal delivery": [ + "HP:0011412" + ], + "vacuum - assisted vaginal delivery": [ + "HP:0011412" + ], + "shoulder dystocia": [ + "HP:0011413" + ], + "hydropic placenta": [ + "HP:0011414" + ], + "hydrops of the placenta": [ + "HP:0011414" + ], + "calcify placenta": [ + "HP:0011415" + ], + "calcified placenta": [ + "HP:0011415" + ], + "placental infarction": [ + "HP:0011416" + ], + "placental thromboembolism": [ + "HP:0011416" + ], + "long umbilical cord": [ + "HP:0011417" + ], + "abnormal insertion of umbilical cord": [ + "HP:0011418" + ], + "placental abruption": [ + "HP:0011419" + ], + "abruptio placenta": [ + "HP:0011419" + ], + "abruptio placentae": [ + "HP:0011419" + ], + "age of death": [ + "HP:0011420" + ], + "death in adolescence": [ + "HP:0011421" + ], + "abnormal blood chloride concentration": [ + "HP:0011422" + ], + "abnormal blood cl concentration": [ + "HP:0011422" + ], + "abnormal blood cl - concentration": [ + "HP:0011422" + ], + "abnormality of chloride homeostasis": [ + "HP:0011422" + ], + "hyperchloremia": [ + "HP:0011423" + ], + "increase serum zinc": [ + "HP:0011424" + ], + "increased serum zinc": [ + "HP:0011424" + ], + "hyperzincemia": [ + "HP:0011424" + ], + "fetal ultrasound soft marker": [ + "HP:0011425" + ], + "foetal ultrasound soft marker": [ + "HP:0011425" + ], + "fetal choroid plexus cyst": [ + "HP:0011426" + ], + "fetal choroid plexus cysts": [ + "HP:0011426" + ], + "foetal choroid plexus cyst": [ + "HP:0011426" + ], + "foetal choroid plexus cysts": [ + "HP:0011426" + ], + "enlarge fetal cisterna magna": [ + "HP:0011427" + ], + "enlarged fetal cisterna magna": [ + "HP:0011427" + ], + "enlarge foetal cisterna magna": [ + "HP:0011427" + ], + "enlarged foetal cisterna magna": [ + "HP:0011427" + ], + "short fetal femur length": [ + 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present at birth": [ + "HP:0011451" + ], + "functional abnormality of the middle ear": [ + "HP:0011452" + ], + "abnormality of the incus": [ + "HP:0011453" + ], + "abnormality of the malleus": [ + "HP:0011454" + ], + "absent malleus": [ + "HP:0011455" + ], + "absent stapes": [ + "HP:0011456" + ], + "loss of eyelash": [ + "HP:0011457" + ], + "loss of eyelashes": [ + "HP:0011457" + ], + "ciliary madarosis": [ + "HP:0011457" + ], + "eyelash fell out": [ + "HP:0011457" + ], + "eyelashes fell out": [ + "HP:0011457" + ], + "milphosis": [ + "HP:0011457" + ], + "miss eyelash": [ + "HP:0011457" + ], + "missing eyelashes": [ + "HP:0011457" + ], + "abdominal symptom": [ + "HP:0011458" + ], + "esophageal carcinoma": [ + "HP:0011459" + ], + "embryonal onset": [ + "HP:0011460" + ], + "fetal onset": [ + "HP:0011461" + ], + "foetal onset": [ + "HP:0011461" + ], + "young adult onset": [ + "HP:0011462" + ], + "childhood onset": [ + "HP:0011463" + ], + "symptom begin in childhood": [ + "HP:0011463" + ], 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villus": [ + "HP:0011473" + ], + "atrophy of small intestinal villi": [ + "HP:0011473" + ], + "biopsy show villous atrophy": [ + "HP:0011473" + ], + "biopsy shows villous atrophy": [ + "HP:0011473" + ], + "duodenal villous atrophy": [ + "HP:0011473" + ], + "small intestine biopsy show villous atrophy": [ + "HP:0011473" + ], + "small intestine biopsy shows villous atrophy": [ + "HP:0011473" + ], + "variable degree of villous atrophy": [ + "HP:0011473" + ], + "villous degeneration": [ + "HP:0011473" + ], + "childhood onset sensorineural hearing impairment": [ + "HP:0011474" + ], + "persistent stapedial artery": [ + "HP:0011475" + ], + "profound sensorineural hearing impairment": [ + "HP:0011476" + ], + "upbeat nystagmus": [ + "HP:0011477" + ], + "true anophthalmia": [ + "HP:0011478" + ], + "complete anophthalmia": [ + "HP:0011478" + ], + "completely miss eyeball": [ + "HP:0011478" + ], + "completely missing eyeball": [ + "HP:0011478" + ], + "total anophthalmia": [ + "HP:0011478" + ], + 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"posterior synechiae": [ + "HP:0011484" + ], + "corneolenticular adhesion": [ + "HP:0011485" + ], + "abnormality of corneal thickness": [ + "HP:0011486" + ], + "increase corneal thickness": [ + "HP:0011487" + ], + "increased corneal thickness": [ + "HP:0011487" + ], + "abnormal corneal endothelium morphology": [ + "HP:0011488" + ], + "abnormality of corneal endothelium": [ + "HP:0011488" + ], + "abnormal migration of corneal endothelium": [ + "HP:0011489" + ], + "abnormal descemet membrane morphology": [ + "HP:0011490" + ], + "abnormality of descemet 's membrane": [ + "HP:0011490" + ], + "reduced number of corneal endothelial cell": [ + "HP:0011491" + ], + "reduced number of corneal endothelial cells": [ + "HP:0011491" + ], + "abnormality of corneal stroma": [ + "HP:0011492" + ], + "central opacification of the cornea": [ + "HP:0011493" + ], + "generalize opacification of the cornea": [ + "HP:0011494" + ], + "generalized opacification of the cornea": [ + "HP:0011494" + ], + "generalised opacification of the cornea": [ + "HP:0011494" + ], + "abnormal corneal epithelium morphology": [ + "HP:0011495" + ], + "abnormality of corneal epithelium": [ + "HP:0011495" + ], + "corneal neovascularization": [ + "HP:0011496" + ], + "corneal neovascularisation": [ + "HP:0011496" + ], + "corneal pannus": [ + "HP:0011496" + ], + "corneal vascularization": [ + "HP:0011496" + ], + "limbal neovascularization": [ + "HP:0011496" + ], + "new blood vessel formation in cornea": [ + "HP:0011496" + ], + "iris neovascularization": [ + "HP:0011497" + ], + "neovascularization of the iris": [ + "HP:0011497" + ], + "new blood vessel formation in iris": [ + "HP:0011497" + ], + "obsolete partial aniridia": [ + "HP:0011498" + ], + "mydriasis": [ + "HP:0011499" + ], + "dilate pupil": [ + "HP:0011499" + ], + "dilated pupil": [ + "HP:0011499" + ], + "polycoria": [ + "HP:0011500" + ], + "multiple pupil": [ + "HP:0011500" + ], + "multiple pupils": [ + "HP:0011500" + ], + "anterior lenticonus": [ 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[ + "HP:0011516" + ], + "rod monochromacy": [ + "HP:0011516" + ], + "rod monochromatism": [ + "HP:0011516" + ], + "cone monochromacy": [ + "HP:0011517" + ], + "dichromacy": [ + "HP:0011518" + ], + "anomalous trichromacy": [ + "HP:0011519" + ], + "deuteranomaly": [ + "HP:0011520" + ], + "deuteranomoly": [ + "HP:0011520" + ], + "green - weak": [ + "HP:0011520" + ], + "deuteranopia": [ + "HP:0011521" + ], + "green - blind": [ + "HP:0011521" + ], + "protanopia": [ + "HP:0011522" + ], + "red - blind": [ + "HP:0011522" + ], + "iris cyst": [ + "HP:0011523" + ], + "iris melanoma": [ + "HP:0011524" + ], + "iris nevus": [ + "HP:0011525" + ], + "eye freckle": [ + "HP:0011525" + ], + "abnormality of lens shape": [ + "HP:0011526" + ], + "lentiglobus": [ + "HP:0011527" + ], + "bulging of eye lens": [ + "HP:0011527" + ], + "solitary congenital hypertrophy of retinal pigment epithelium": [ + "HP:0011528" + ], + "single isolate chrpe": [ + "HP:0011528" + ], + "single isolated chrpe": [ + "HP:0011528" + ], + "single isolate congenital hypertrophy of retinal pigment epithelium": [ + "HP:0011528" + ], + "single isolated congenital hypertrophy of retinal pigment epithelium": [ + "HP:0011528" + ], + "multiple bilateral congenital hypertrophy of retinal pigment epithelium": [ + "HP:0011529" + ], + "multiple bilateral chrpe": [ + "HP:0011529" + ], + "retinal hole": [ + "HP:0011530" + ], + "retinal holes": [ + "HP:0011530" + ], + "vitritis": [ + "HP:0011531" + ], + "hyalitis": [ + "HP:0011531" + ], + "vitreitis": [ + "HP:0011531" + ], + "subretinal exudate": [ + "HP:0011532" + ], + "snowflake vitreoretinal degeneration": [ + "HP:0011533" + ], + "snowflake retinal degeneration": [ + "HP:0011533" + ], + "abnormal spatial orientation of the cardiac segment": [ + "HP:0011534" + ], + "abnormal spatial orientation of the cardiac segments": [ + "HP:0011534" + ], + "abnormal atrial arrangement": [ + "HP:0011535" + ], + "abnormal location of heart atrium": [ + "HP:0011535" + ], + "right atrial isomerism": [ + "HP:0011536" + ], + "leave atrial isomerism": [ + "HP:0011537" + ], + "left atrial isomerism": [ + "HP:0011537" + ], + "atrial situs inversus": [ + "HP:0011538" + ], + "atrial situs ambiguous": [ + "HP:0011539" + ], + "atrial heterotaxy": [ + "HP:0011539" + ], + "atrial situs ambiguus": [ + "HP:0011539" + ], + "congenitally correct transposition of the great artery": [ + "HP:0011540" + ], + "congenitally corrected transposition of the great arteries": [ + "HP:0011540" + ], + "l - transposition": [ + "HP:0011540" + ], + "ventricular inversion": [ + "HP:0011540" + ], + "criss - cross atrioventricular valve": [ + "HP:0011541" + ], + "criss - cross atrioventricular valves": [ + "HP:0011541" + ], + "criss - cross atrioventricular valve with superior - inferior ventricle": [ + "HP:0011542" + ], + "criss - cross atrioventricular valves with superior - inferior ventricles": [ + "HP:0011542" + ], + "superior - inferior ventricle without criss - cross atrioventricular valve": [ + "HP:0011543" + ], + "superior - inferior ventricles without criss - cross atrioventricular valves": [ + "HP:0011543" + ], + "l - looping of the right ventricle": [ + "HP:0011544" + ], + "abnormal connection of the cardiac segment": [ + "HP:0011545" + ], + "abnormal connection of the cardiac segments": [ + "HP:0011545" + ], + "abnormal connexion of the cardiac segment": [ + "HP:0011545" + ], + "abnormal connexion of the cardiac segments": [ + "HP:0011545" + ], + "discordant connection of the cardiac segment": [ + "HP:0011545" + ], + "discordant connection of the cardiac segments": [ + "HP:0011545" + ], + "abnormal atrioventricular connection": [ + "HP:0011546" + ], + "abnormal atrioventricular connexion": [ + "HP:0011546" + ], + "absent leave sided atrioventricular connection": [ + "HP:0011547" + ], + "absent left sided atrioventricular connection": [ + "HP:0011547" + ], + "absent leave sided atrioventricular connexion": [ + "HP:0011547" + ], + "absent left sided atrioventricular connexion": [ + "HP:0011547" + ], + "absent right side atrioventricular connection": [ + "HP:0011548" + ], + "absent right sided atrioventricular connection": [ + "HP:0011548" + ], + "absent right side atrioventricular connexion": [ + "HP:0011548" + ], + "absent right sided atrioventricular connexion": [ + "HP:0011548" + ], + "univentricular heart with absent left side atrioventricular connection": [ + "HP:0011549" + ], + "univentricular heart with absent left sided atrioventricular connection": [ + "HP:0011549" + ], + "univentricular heart with absent left side atrioventricular connexion": [ + "HP:0011549" + ], + "univentricular heart with absent left sided atrioventricular connexion": [ + "HP:0011549" + ], + "biventricular heart with straddle right side atrioventricular valve and absent leave sided atrioventricular connection": [ + "HP:0011550" + ], + "biventricular heart with straddling right sided atrioventricular valve and absent left sided atrioventricular connection": [ + "HP:0011550" + ], + "right side atrium to leave ventricle and absent leave sided atrioventricular connection": [ + "HP:0011551" + ], + "right sided atrium to left ventricle and absent left sided atrioventricular connection": [ + "HP:0011551" + ], + "right side atrium to leave ventricle and absent leave sided atrioventricular connexion": [ + "HP:0011551" + ], + "right sided atrium to left ventricle and absent left sided atrioventricular connexion": [ + "HP:0011551" + ], + "ambiguous atrioventricular connection": [ + "HP:0011552" + ], + "ambiguous atrioventricular connexion": [ + "HP:0011552" + ], + "discordant atrioventricular connection": [ + "HP:0011553" + ], + "discordant atrioventricular connexion": [ + "HP:0011553" + ], + "double inlet atrioventricular connection": [ + "HP:0011554" + ], + "double inlet atrioventricular connexion": [ + "HP:0011554" + ], + "double inlet leave ventricle": [ + "HP:0011555" + ], + "double inlet left ventricle": [ + "HP:0011555" + ], + "double inlet right ventricle": [ + "HP:0011556" + ], + "double inlet to single ventricle of indeterminate morphology": [ + "HP:0011557" + ], + "double inlet to single ventricle with common atrioventricular orifice": [ + "HP:0011558" + ], + "double inlet to single ventricle with two atrioventricular valve": [ + "HP:0011559" + ], + "double inlet to single ventricle with two atrioventricular valves": [ + "HP:0011559" + ], + "mitral atresia": [ + "HP:0011560" + ], + "mitral valve atresia": [ + "HP:0011560" + ], + "override atrioventricular valve": [ + "HP:0011561" + ], + "overriding atrioventricular valve": [ + "HP:0011561" + ], + "straddle atrioventricular valve": [ + "HP:0011562" + ], + "straddling atrioventricular valve": [ + "HP:0011562" + ], + "abnormal ventriculoarterial connection": [ + "HP:0011563" + ], + "abnormal ventriculo - arterial connection": [ + "HP:0011563" + ], + "abnormal ventriculoarterial connexion": [ + "HP:0011563" + ], + "mitral valve arcade": [ + "HP:0011564" + ], + "hammock mitral valve": [ + "HP:0011564" + ], + "common atrium": [ + "HP:0011565" + ], + "single atrium": [ + "HP:0011565" + ], + "cor triatriatum dexter": [ + "HP:0011566" + ], + "cor triatriatum dextrum": [ + "HP:0011566" + ], + "sinus venosus atrial septal defect": [ + "HP:0011567" + ], + "double orifice mitral valve": [ + "HP:0011568" + ], + "cleft anterior mitral valve leaflet": [ + "HP:0011569" + ], + "congenital mitral stenosis": [ + "HP:0011570" + ], + "parachute mitral valve": [ + "HP:0011571" + ], + "supramitral ring": [ + "HP:0011572" + ], + "membranous supravalvular mitral stenosis": [ + "HP:0011572" + ], + "supravalvular mitral ring": [ + "HP:0011572" + ], + "hypoplastic tricuspid valve": [ + "HP:0011573" + ], + "tricuspid valve hypoplasia": [ + "HP:0011573" + ], + "underdeveloped tricuspid valve": [ + "HP:0011573" + ], + "imperforate atrioventricular valve": [ + "HP:0011574" + ], + "unopened atrioventricular valve": [ + "HP:0011574" + ], + "imperforate tricuspid valve": [ + "HP:0011575" + ], + "unopened tricuspid valve": [ + "HP:0011575" + ], + "intermediate atrioventricular canal defect": [ + "HP:0011576" + ], + "intermediate atrioventricular septal defect": [ + "HP:0011576" + ], + "partial atrioventricular canal defect": [ + "HP:0011577" + ], + "transitional atrioventricular canal defect": [ + "HP:0011578" + ], + "unbalanced atrioventricular canal defect": [ + "HP:0011579" + ], + "unbalanced atrioventricular septal defect": [ + "HP:0011579" + ], + "short chordae tendineae of the mitral valve": [ + "HP:0011580" + ], + "double outlet leave ventricle": [ + "HP:0011581" + ], + "double outlet left ventricle": [ + "HP:0011581" + ], + "abdominal ectopia cordis": [ + "HP:0011582" + ], + "cervical ectopia cordis": [ + "HP:0011583" + ], + "thoracocervical ectopia cordis": [ + "HP:0011584" + ], + "thoracic ectopia cordis": [ + "HP:0011585" + ], + "thoracoabdominal ectopia cordis": [ + "HP:0011586" + ], + "abnormal branch pattern of the aortic arch": [ + "HP:0011587" + ], + "abnormal branching pattern of the aortic arch": [ + "HP:0011587" + ], + "cervical aortic arch": [ + "HP:0011588" + ], + "common origin of the right brachiocephalic artery and leave common carotid artery": [ + "HP:0011589" + ], + "common origin of the right brachiocephalic artery and left common carotid artery": [ + "HP:0011589" + ], + "bovine arch": [ + "HP:0011589" + ], + "common brachiocephalic trunk": [ + "HP:0011589" + ], + "ovine arch": [ + "HP:0011589" + ], + "double aortic arch": [ + "HP:0011590" + ], + "leave aortic arch with cervical origin of the right subclavian artery": [ + "HP:0011591" + ], + "left aortic arch with cervical origin of the right subclavian artery": [ + "HP:0011591" + ], + "leave aortic arch with isolated subclavian artery": [ + "HP:0011592" + ], + "left aortic arch with isolated subclavian artery": [ + "HP:0011592" + ], + "leave aortic arch with retroesophageal diverticulum of kommerell": [ + "HP:0011593" + ], + "left aortic arch with retroesophageal diverticulum of kommerell": [ + "HP:0011593" + ], + "kommerell diverticulum": [ + "HP:0011593" + ], + "right aortic arch with retroesophageal diverticulum of kommerell": [ + "HP:0011594" + ], + "leave aortic arch with retroesophageal right subclavian artery": [ + "HP:0011595" + ], + "left aortic arch with retroesophageal right subclavian artery": [ + "HP:0011595" + ], + "leave aortic arch with right descend aorta and right ductus arteriosus": [ + "HP:0011596" + ], + "left aortic arch with right descending aorta and right ductus arteriosus": [ + "HP:0011596" + ], + "right aortic arch with left descend aorta and leave ductus arteriosus": [ + "HP:0011597" + ], + "right aortic arch with left descending aorta and left ductus arteriosus": [ + "HP:0011597" + ], + "right aortic arch with retroesophageal leave subclavian artery": [ + "HP:0011598" + ], + "right aortic arch with retroesophageal left subclavian artery": [ + "HP:0011598" + ], + "right aortic arch with aberrant leave subclavian artery": [ + "HP:0011598" + ], + "right aortic arch with aberrant left subclavian artery": [ + "HP:0011598" + ], + "right aortic arch with anomalous left subclavian artery": [ + "HP:0011598" + ], + "mesocardia": [ + "HP:0011599" + ], + "abnormal direction of ventricular apex": [ + "HP:0011600" + ], + "rightward direction of ventricular apex": [ + "HP:0011601" + ], + "midline direction of ventricular apex": [ + "HP:0011602" + ], + "congenital malformation of the great artery": [ + "HP:0011603" + ], + "congenital malformation of the great arteries": [ + "HP:0011603" + ], + "aortopulmonary window": [ + "HP:0011604" + ], + "congenitally correct transposition of the great artery with ventricular septal defect": [ + "HP:0011605" + ], + "congenitally corrected transposition of the great arteries with ventricular septal defect": [ + "HP:0011605" + ], + "cctga": [ + "HP:0011605" + ], + "obsolete transposition of the great artery with intact ventricular septum": [ + "HP:0011606" + ], + "obsolete transposition of the great arteries with intact ventricular septum": [ + "HP:0011606" + ], + "obsolete transposition of the great artery with ventricular septal defect": [ + "HP:0011607" + ], + "obsolete transposition of the great arteries with ventricular septal defect": [ + "HP:0011607" + ], + "type ii truncus arteriosus": [ + "HP:0011608" + ], + "persistent truncus arteriosus type ii": [ + "HP:0011608" + ], + "type 2 truncus arteriosus": [ + "HP:0011608" + ], + "type iii truncus arteriosus": [ + "HP:0011609" + ], + "persistent truncus arteriosus type iii": [ + "HP:0011609" + ], + "type 3 truncus arteriosus": [ + "HP:0011609" + ], + "type iv truncus arteriosus": [ + "HP:0011610" + ], + "persistent truncus arteriosus type iv": [ + "HP:0011610" + ], + "type 4 truncus arteriosus": [ + "HP:0011610" + ], + "interrupt aortic arch": [ + "HP:0011611" + ], + "interrupted aortic arch": [ + "HP:0011611" + ], + "aortic arch obstruction": [ + "HP:0011611" + ], + "atretic transverse aortic arch": [ + "HP:0011611" + ], + "interrupt aortic arch type a": [ + "HP:0011612" + ], + "interrupted aortic arch type a": [ + "HP:0011612" + ], + "interrupt aortic arch type b": [ + "HP:0011613" + ], + "interrupted aortic arch type b": [ + "HP:0011613" + ], + "interrupt aortic arch , type b": [ + "HP:0011613" + ], + "interrupted aortic arch , type b": [ + "HP:0011613" + ], + "interrupt aortic arch type c": [ + "HP:0011614" + ], + "interrupted aortic arch type c": [ + "HP:0011614" + ], + "abnormal pulmonary situs morphology": [ + "HP:0011615" + ], + "abnormality of pulmonary situs": [ + "HP:0011615" + ], + "pulmonary situs inversus": [ + "HP:0011616" + ], + "pulmonary situs ambiguus": [ + "HP:0011617" + ], + "pulmonary situs ambiguus with bilateral morphologic right lung": [ + "HP:0011618" + ], + "pulmonary situs ambiguus with bilateral morphologic right lungs": [ + "HP:0011618" + ], + "pulmonary situs ambiguus with bilateral morphologic leave lung": [ + "HP:0011619" + ], + "pulmonary situs ambiguus with bilateral morphologic left lungs": [ + "HP:0011619" + ], + "abnormality of abdominal situs": [ + "HP:0011620" + ], + "gerbode ventricular septal defect": [ + "HP:0011621" + ], + "leave ventricular - right atrial communication": [ + "HP:0011621" + ], + "left ventricular - right atrial communication": [ + "HP:0011621" + ], + "inlet ventricular septal defect": [ + "HP:0011622" + ], + "atrioventricular canal type ventricular septal defect": [ + "HP:0011622" + ], + "type 3 ventricular septal defect": [ + "HP:0011622" + ], + "muscular ventricular septal defect": [ + "HP:0011623" + ], + "type 4 ventricular septal defect": [ + "HP:0011623" + ], + "ventricular septal defect , muscular": [ + "HP:0011623" + ], + "apical muscular ventricular septal defect": [ + "HP:0011624" + ], + "multiple muscular ventricular septal defect": [ + "HP:0011625" + ], + "multiple muscular ventricular septal defects": [ + "HP:0011625" + ], + "swiss cheese ventricular septal defect": [ + "HP:0011625" + ], + "scimitar anomaly": [ + "HP:0011626" + ], + "pulmonary venolobar syndrome": [ + "HP:0011626" + ], + "scimitar syndrome": [ + "HP:0011626" + ], + "aorto - ventricular tunnel": [ + "HP:0011627" + ], + "congenital defect of the pericardium": [ + "HP:0011628" + ], + "total absence of the pericardium": [ + "HP:0011629" + ], + "absent pericardium": [ + "HP:0011629" + ], + "congenital absence of the pericardium": [ + "HP:0011629" + ], + "complete diaphragmatic absence of pericardium": [ + "HP:0011630" + ], + "complete right side absence of pericardium": [ + "HP:0011631" + ], + "complete right sided absence of pericardium": [ + "HP:0011631" + ], + "partial right side absence of pericardium": [ + "HP:0011632" + ], + "partial right sided absence of pericardium": [ + "HP:0011632" + ], + "complete leave sided absence of pericardium": [ + "HP:0011633" + ], + "complete left sided absence of pericardium": [ + "HP:0011633" + ], + "absent line around of left side of heart": [ + "HP:0011633" + ], + "absent lining around of left side of heart": [ + "HP:0011633" + ], + "partial leave sided absence of pericardium": [ + "HP:0011634" + ], + "partial left sided absence of pericardium": [ + "HP:0011634" + ], + "partial diaphragmatic absence of pericardium": [ + "HP:0011635" + ], + "abnormal coronary artery origin": [ + "HP:0011636" + ], + "anomalous origin of coronary artery from the pulmonary artery": [ + "HP:0011637" + ], + "anomalous origin of left coronary artery from the pulmonary artery": [ + "HP:0011638" + ], + "anomalous leave coronary artery from the pulmonary artery": [ + "HP:0011638" + ], + "anomalous left coronary artery from the pulmonary artery": [ + "HP:0011638" + ], + "bland - garland - white syndrome": [ + "HP:0011638" + ], + "anomalous origin of right coronary artery from the pulmonary artery": [ + "HP:0011639" + ], + "single coronary artery origin": [ + "HP:0011640" + ], + "coronary artery fistula": [ + "HP:0011641" + ], + "coronary fistula": [ + "HP:0011641" + ], + "abnormal coronary sinus morphology": [ + "HP:0011642" + ], + "abnormality of the coronary sinus": [ + "HP:0011642" + ], + "coronary sinus atrial septal defect": [ + "HP:0011643" + ], + "coronary sinus diverticulum": [ + "HP:0011644" + ], + "diverticulum of the coronary sinus": [ + "HP:0011644" + ], + "dilatation of the sinus of valsalva": [ + "HP:0011645" + ], + "aneurysm of the aortic sinus": [ + "HP:0011645" + ], + "aortic sinus aneurysm": [ + "HP:0011645" + ], + "sinus of valsalva aneurysm": [ + "HP:0011645" + ], + "juxtaductal coarctation of the aorta": [ + "HP:0011646" + ], + "postductal coarctation of the aorta": [ + "HP:0011647" + ], + "postductal aortic coarctation": [ + "HP:0011647" + ], + "patent ductus arteriosus after birth at term": [ + "HP:0011648" + ], + "patent ductus arteriosus after premature birth": [ + "HP:0011649" + ], + "bilateral ductus arteriosus": [ + "HP:0011650" + ], + "bilateral ductus botalli": [ + "HP:0011650" + ], + "double outlet right ventricle with doubly commit ventricular septal defect and pulmonary stenosis": [ + "HP:0011651" + ], + "double outlet right ventricle with doubly committed ventricular septal defect and pulmonary stenosis": [ + "HP:0011651" + ], + "dorv with doubly commit vsd and pulmonary stenosis": [ + "HP:0011651" + ], + "dorv with doubly committed vsd and pulmonary stenosis": [ + "HP:0011651" + ], + "double outlet right ventricle with doubly commit ventricular septal defect without pulmonary stenosis": [ + "HP:0011652" + ], + "double outlet right ventricle with doubly committed ventricular septal defect without pulmonary stenosis": [ + "HP:0011652" + ], + "dorv with doubly commit vsd": [ + "HP:0011652" + ], + "dorv with doubly committed vsd": [ + "HP:0011652" + ], + "double outlet right ventricle , doubly commit ventricular septal defect": [ + "HP:0011652" + ], + "double outlet right ventricle , doubly committed ventricular septal defect": [ + "HP:0011652" + ], + "double outlet right ventricle with non - committed ventricular septal defect and pulmonary stenosis": [ + "HP:0011653" + ], + "dorv with non - commit vsd and pulmonary stenosis": [ + "HP:0011653" + ], + "dorv with non - committed vsd and pulmonary stenosis": [ + "HP:0011653" + ], + "double outlet right ventricle with non - committed ventricular septal defect without pulmonary stenosis": [ + "HP:0011654" + ], + "dorv with non - committed vsd without pulmonary stenosis": [ + "HP:0011654" + ], + "double outlet right ventricle , noncommitted ventricular septal defect": [ + "HP:0011654" + ], + "double outlet right ventricle with subaortic ventricular septal defect and pulmonary stenosis": [ + "HP:0011655" + ], + "dorv with subaortic vsd and pulmonary stenosis": [ + "HP:0011655" + ], + "double outlet right ventricle with subaortic ventricular septal defect without pulmonary stenosis": [ + "HP:0011656" + ], + "dorv with subaortic vsd without pulmonary stenosis": [ + "HP:0011656" + ], + "double outlet right ventricle with subpulmonary ventricular septal defect and pulmonary stenosis": [ + "HP:0011657" + ], + "dorv with subpulmonary vsd and pulmonary stenosis": [ + "HP:0011657" + ], + "double outlet right ventricle with subpulmonary ventricular septal defect without pulmonary stenosis": [ + "HP:0011658" + ], + "dorv with subpulmonary vsd without pulmonary stenosis": [ + "HP:0011658" + ], + "taussig - bing anomaly": [ + "HP:0011658" + ], + "tetralogy of fallot with absent pulmonary valve": [ + "HP:0011659" + ], + "tetralogy of fallot with absent pulmonary valve syndrome": [ + "HP:0011659" + ], + "anomalous origin of one pulmonary artery from ascend aorta": [ + "HP:0011660" + ], + "anomalous origin of one pulmonary artery from ascending aorta": [ + "HP:0011660" + ], + "hemitruncus": [ + "HP:0011660" + ], + "anomalous origin of left pulmonary artery from ascend aorta": [ + "HP:0011661" + ], + "anomalous origin of left pulmonary artery from ascending aorta": [ + "HP:0011661" + ], + "tricuspid atresia": [ + "HP:0011662" + ], + "tricuspid valve atresia": [ + "HP:0011662" + ], + "right ventricular cardiomyopathy": [ + "HP:0011663" + ], + "cardiomyopathy , esp . right ventricular": [ + "HP:0011663" + ], + "cardiomyopathy , right ventricular": [ + "HP:0011663" + ], + "leave ventricular noncompaction cardiomyopathy": [ + "HP:0011664" + ], + "left ventricular noncompaction cardiomyopathy": [ + "HP:0011664" + ], + "leave ventricular non - compaction cardiomyopathy": [ + "HP:0011664" + ], + "left ventricular non - compaction cardiomyopathy": [ + "HP:0011664" + ], + "takotsubo cardiomyopathy": [ + "HP:0011665" + ], + "broken - heart syndrome": [ + "HP:0011665" + ], + "absent right superior vena cava": [ + "HP:0011666" + ], + "bilateral superior vena cava with bridging vein": [ + "HP:0011667" + ], + "bilateral superior vena cava with no bridging vein": [ + "HP:0011668" + ], + "leave superior vena cava drain directly to the left atrium": [ + "HP:0011669" + ], + "left superior vena cava draining directly to the left atrium": [ + "HP:0011669" + ], + "leave superior vena cava drain to coronary sinus": [ + "HP:0011670" + ], + "left superior vena cava draining to coronary sinus": [ + "HP:0011670" + ], + "interrupt inferior vena cava with azygous continuation": [ + "HP:0011671" + ], + "interrupted inferior vena cava with azygous continuation": [ + "HP:0011671" + ], + "cardiac myxoma": [ + "HP:0011672" + ], + "cardiac hemangioma": [ + "HP:0011673" + ], + "cardiac teratoma": [ + "HP:0011674" + ], + "arrhythmia": [ + "HP:0011675" + ], + "abnormal heart rate": [ + "HP:0011675" + ], + "arrhythmias": [ + "HP:0011675" + ], + "cardiac arrhythmia": [ + "HP:0011675" + ], + "cardiac arrhythmias": [ + "HP:0011675" + ], + "cardiac rhythm disturbance": [ + "HP:0011675" + ], + "cardiac rhythm disturbances": [ + "HP:0011675" + ], + "heart rhythm disorder": [ + "HP:0011675" + ], + "heart rhythm disorders": [ + "HP:0011675" + ], + "irregular heart beat": [ + "HP:0011675" + ], + "irregular heartbeat": [ + "HP:0011675" + ], + "tetralogy of fallot with absent subarterial conus": [ + "HP:0011676" + ], + "tetralogy of fallot with atrioventricular canal defect": [ + "HP:0011677" + ], + "tetralogy of fallot with pulmonary atresia and major aortopulmonary collateral artery": [ + "HP:0011678" + ], + "tetralogy of fallot with pulmonary atresia and major aortopulmonary collateral arteries": [ + "HP:0011678" + ], + "tetralogy of fallot with pulmonary stenosis": [ + "HP:0011679" + ], + "single ventricle of indeterminate morphology": [ + "HP:0011680" + ], + "subarterial ventricular septal defect": [ + "HP:0011681" + ], + "conal ventricular septal defect": [ + "HP:0011681" + ], + "doubly commit ventricular septal defect": [ + "HP:0011681" + ], + "doubly committed ventricular septal defect": [ + "HP:0011681" + ], + "infundibular ventricular septal defect": [ + "HP:0011681" + ], + "supracristal ventricular septal defect": [ + "HP:0011681" + ], + "type 1 ventricular septal defect": [ + 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tachycardia with a manifest accessory pathway": [ + "HP:0011694" + ], + "cerebellar hemorrhage": [ + "HP:0011695" + ], + "cerebellar haemorrhage": [ + "HP:0011695" + ], + "supraventricular tachycardia with a manifest accessory pathway on the left free wall": [ + "HP:0011696" + ], + "supraventricular tachycardia with a manifest accessory pathway on the right free wall": [ + "HP:0011697" + ], + "supraventricular tachycardia with a manifest accessory pathway on the septum": [ + "HP:0011698" + ], + "atrial reentry tachycardia": [ + "HP:0011699" + ], + "automatic atrial tachycardia": [ + "HP:0011700" + ], + "multifocal atrial tachycardia": [ + "HP:0011701" + ], + "chaotic atrial tachycardia": [ + "HP:0011701" + ], + "ectopic atrial tachycardia": [ + "HP:0011701" + ], + "abnormal electrophysiology of sinoatrial node origin": [ + "HP:0011702" + ], + "sinus tachycardia": [ + "HP:0011703" + ], + "sinus tach": [ + "HP:0011703" + ], + "sinus tachy": [ + "HP:0011703" + ], + "sick sinus syndrome": [ + "HP:0011704" + ], + "sinoatrial node disease": [ + "HP:0011704" + ], + "first degree atrioventricular block": [ + "HP:0011705" + ], + "second degree atrioventricular block": [ + "HP:0011706" + ], + "mobitz i atrioventricular block": [ + "HP:0011707" + ], + "mobitz type 1 atrioventricular block": [ + "HP:0011707" + ], + "wenckebach block": [ + "HP:0011707" + ], + "mobitz ii atrioventricular block": [ + "HP:0011708" + ], + "mobitz type 2 atrioventricular block": [ + "HP:0011708" + ], + "atrioventricular dissociation": [ + "HP:0011709" + ], + "bundle branch block": [ + "HP:0011710" + ], + "bundle - branch block": [ + "HP:0011710" + ], + "leave anterior fascicular block": [ + "HP:0011711" + ], + "left anterior fascicular block": [ + "HP:0011711" + ], + "leave anterior hemiblock": [ + "HP:0011711" + ], + "left anterior hemiblock": [ + "HP:0011711" + ], + "right bundle branch block": [ + "HP:0011712" + ], + "right bundle - branch block": [ + "HP:0011712" + ], + "leave bundle branch block": [ + "HP:0011713" + ], + "left bundle branch block": [ + "HP:0011713" + ], + "libman - sack lesion": [ + "HP:0011714" + ], + "libman - sacks lesions": [ + "HP:0011714" + ], + "trifascicular block": [ + "HP:0011715" + ], + "junctional ectopic tachycardia": [ + "HP:0011716" + ], + "atrioventricular reentrant tachycardia": [ + "HP:0011717" + ], + "av nodal reentry tachycardia": [ + "HP:0011717" + ], + "abnormality of the pulmonary vein": [ + "HP:0011718" + ], + "abnormality of the pulmonary veins": [ + "HP:0011718" + ], + "abnormality of lung vein": [ + "HP:0011718" + ], + "abnormality of lung veins": [ + "HP:0011718" + ], + "supracardiac total anomalous pulmonary venous connection": [ + "HP:0011719" + ], + "supracardiac total anomalous pulmonary venous connexion": [ + "HP:0011719" + ], + "total anomalous pulmonary venous connection , supracardiac": [ + "HP:0011719" + ], + "type 1 total anomalous pulmonary venous connection": [ + "HP:0011719" + ], + "cardiac total anomalous 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tachycardia": [ + "HP:0011725" + ], + "persistent fetal circulation": [ + "HP:0011726" + ], + "persistent foetal circulation": [ + "HP:0011726" + ], + "peroneal muscle weakness": [ + "HP:0011727" + ], + "fibularis muscle weakness": [ + "HP:0011727" + ], + "elbow clonus": [ + "HP:0011728" + ], + "abnormality of joint mobility": [ + "HP:0011729" + ], + "abnormal central sensory function": [ + "HP:0011730" + ], + "abnormality of central sensory function": [ + "HP:0011730" + ], + "abnormality of circulate cortisol level": [ + "HP:0011731" + ], + "abnormality of circulating cortisol level": [ + "HP:0011731" + ], + "abnormality of adrenal morphology": [ + "HP:0011732" + ], + "abnormality of adrenal physiology": [ + "HP:0011733" + ], + "central adrenal insufficiency": [ + "HP:0011734" + ], + "secondary adrenal insufficiency": [ + "HP:0011734" + ], + "adrenocorticotropin deficient adrenal insufficiency": [ + "HP:0011735" + ], + "acth deficient adrenal insufficiency": [ + "HP:0011735" + ], + "primary hyperaldosteronism": [ + "HP:0011736" + ], + "corticotropin - release hormone deficient adrenal insufficiency": [ + "HP:0011737" + ], + "corticotropin - releasing hormone deficient adrenal insufficiency": [ + "HP:0011737" + ], + "crh deficient adrenal insufficiency": [ + "HP:0011737" + ], + "tertiary adrenal insufficiency": [ + "HP:0011737" + ], + "corticotropin - release hormone receptor defect": [ + "HP:0011738" + ], + "corticotropin - releasing hormone receptor defect": [ + "HP:0011738" + ], + "corticotropin - release hormone receptor ( crhr ) resistance": [ + "HP:0011738" + ], + "corticotropin - releasing hormone receptor ( crhr ) resistance": [ + "HP:0011738" + ], + "crhr defect": [ + "HP:0011738" + ], + "dexamethasone - suppressible primary hyperaldosteronism": [ + "HP:0011739" + ], + "familial primary hyperaldosteronism type 1": [ + "HP:0011739" + ], + "glucocorticoid - remediable familial primary aldosteronism": [ + "HP:0011739" + ], + "glucocortocoid - insensitive primary hyperaldosteronism": [ + "HP:0011740" + ], + "familial primary hyperaldosteronism type 2": [ + "HP:0011740" + ], + "secondary hyperaldosteronism": [ + "HP:0011741" + ], + "hyperreninemic hyperaldosteronism": [ + "HP:0011741" + ], + "ectopic adrenal gland": [ + "HP:0011742" + ], + "abnormal adrenal gland position": [ + "HP:0011742" + ], + "adrenal gland agenesis": [ + "HP:0011743" + ], + "secondary hypercortisolism": [ + "HP:0011744" + ], + "acth - dependent hypercortisolemia": [ + "HP:0011744" + ], + "non - secretory adrenocortical adenoma": [ + "HP:0011745" + ], + "non - secretory adrenal adenoma": [ + "HP:0011745" + ], + "secretory adrenocortical adenoma": [ + "HP:0011746" + ], + "secretory adrenal adenoma": [ + "HP:0011746" + ], + "abnormality of the anterior pituitary": [ + "HP:0011747" + ], + "pituitary disease": [ + "HP:0011747" + ], + "adrenocorticotropic hormone deficiency": [ + "HP:0011748" + ], + "acth deficiency": [ + "HP:0011748" + ], + "corticotropin deficiency": [ 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agenesis": [ + "HP:0011756" + ], + "posterior pituitary hypoplasia": [ + "HP:0011757" + ], + "neurohypophysis hypoplasia": [ + "HP:0011757" + ], + "pituitary acidophilic stem cell adenoma": [ + "HP:0011758" + ], + "pituitary gonadotropic cell adenoma": [ + "HP:0011759" + ], + "pituitary gonadotropinoma": [ + "HP:0011759" + ], + "pituitary growth hormone cell adenoma": [ + "HP:0011760" + ], + "pituitary somatotropinoma": [ + "HP:0011760" + ], + "pituitary null cell adenoma": [ + "HP:0011761" + ], + "clinically silent pituitary adenoma": [ + "HP:0011761" + ], + "hormonally silent pituitary adenoma": [ + "HP:0011761" + ], + "non - functional pituitary adenoma": [ + "HP:0011761" + ], + "silent pituitary adenoma": [ + "HP:0011761" + ], + "pituitary thyrotropic cell adenoma": [ + "HP:0011762" + ], + "pituitary thyrotropinoma": [ + "HP:0011762" + ], + "pituitary carcinoma": [ + "HP:0011763" + ], + "pituitary spindle cell oncocytoma": [ + "HP:0011764" + ], + "obsolete ectopic anterior pituitary": [ + "HP:0011765" + ], + "abnormality of the parathyroid morphology": [ + "HP:0011766" + ], + "abnormality of the parathyroid physiology": [ + "HP:0011767" + ], + "parathyroid dysfunction": [ + "HP:0011767" + ], + "parathyroid issue": [ + "HP:0011767" + ], + "parathyroid dysgenesis": [ + "HP:0011768" + ], + "ectopic parathyroid": [ + "HP:0011769" + ], + "tertiary hyperparathyroidism": [ + "HP:0011770" + ], + "autoimmune hypoparathyroidism": [ + "HP:0011771" + ], + "abnormal thyroid morphology": [ + "HP:0011772" + ], + "abnormal shape of thyroid gland": [ + "HP:0011772" + ], + "abnormality of thyroid morphology": [ + "HP:0011772" + ], + "uninodular goiter": [ + "HP:0011773" + ], + "uninodular goitre": [ + "HP:0011773" + ], + "thyroid follicular adenoma": [ + "HP:0011774" + ], + "thyroid macrofollicular adenoma": [ + "HP:0011775" + ], + "thyroid microfollicular adenoma": [ + "HP:0011776" + ], + "thyroid papillary adenoma": [ + "HP:0011777" + ], + "thyroid atypical adenoma": [ 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serum free t3": [ + "HP:0011788" + ], + "increase serum free triiodothyronine": [ + "HP:0011788" + ], + "increased serum free triiodothyronine": [ + "HP:0011788" + ], + "increase serum ft3": [ + "HP:0011788" + ], + "increased serum ft3": [ + "HP:0011788" + ], + "impaired sensitivity to thyroid stimulate hormone": [ + "HP:0011789" + ], + "impaired sensitivity to thyroid stimulating hormone": [ + "HP:0011789" + ], + "thyroid - stimulate hormone receptor defect": [ + "HP:0011789" + ], + "thyroid - stimulating hormone receptor defect": [ + "HP:0011789" + ], + "tshr defect": [ + "HP:0011789" + ], + "activate thyroid - stimulate hormone receptor defect": [ + "HP:0011790" + ], + "activating thyroid - stimulating hormone receptor defect": [ + "HP:0011790" + ], + "activate tshr defect": [ + "HP:0011790" + ], + "activating tshr defect": [ + "HP:0011790" + ], + "inactivate thyroid - stimulate hormone receptor defect": [ + "HP:0011791" + ], + "inactivating thyroid - stimulating hormone receptor defect": [ + "HP:0011791" + ], + "inactivate tshr defect": [ + "HP:0011791" + ], + "inactivating tshr defect": [ + "HP:0011791" + ], + "neoplasm by histology": [ + "HP:0011792" + ], + "neoplasm by anatomical site": [ + "HP:0011793" + ], + "embryonal renal neoplasm": [ + "HP:0011794" + ], + "intralobar nephroblastomatosis": [ + "HP:0011795" + ], + "perilobar nephroblastomatosis": [ + "HP:0011796" + ], + "papillary renal cell carcinoma type 1": [ + "HP:0011797" + ], + "renal oncocytoma": [ + "HP:0011798" + ], + "abnormality of facial soft tissue": [ + "HP:0011799" + ], + "anomaly of facial soft tissue": [ + "HP:0011799" + ], + "deformity of facial soft tissue": [ + "HP:0011799" + ], + "malformation of facial soft tissue": [ + "HP:0011799" + ], + "midface retrusion": [ + "HP:0011800" + ], + "decreased projection of midface": [ + "HP:0011800" + ], + "decreased size of midface": [ + "HP:0011800" + ], + "flat midface": [ + "HP:0011800" + ], + "hypoplasia of midface": [ + "HP:0011800" + ], + "hypotrophic midface": [ + "HP:0011800" + ], + "midface deficiency": [ + "HP:0011800" + ], + "midface hypoplasia": [ + "HP:0011800" + ], + "midface , flat": [ + "HP:0011800" + ], + "retrusive midface": [ + "HP:0011800" + ], + "small midface": [ + "HP:0011800" + ], + "underdevelopment of midface": [ + "HP:0011800" + ], + "enlargement of parotid gland": [ + "HP:0011801" + ], + "hyperplasia of parotid gland": [ + "HP:0011801" + ], + "hypertrophy of parotid gland": [ + "HP:0011801" + ], + "increase size of parotid gland": [ + "HP:0011801" + ], + "increased size of parotid gland": [ + "HP:0011801" + ], + "hamartoma of tongue": [ + "HP:0011802" + ], + "lingual hamartoma": [ + "HP:0011802" + ], + "bifid nose": [ + "HP:0011803" + ], + "bifid nasal bridge": [ + "HP:0011803" + ], + "cleft nasal bridge": [ + "HP:0011803" + ], + "cleft nose": [ + "HP:0011803" + ], + "indentation or clefting of the nose": [ + "HP:0011803" + ], + "indent bridge of nose": [ + "HP:0011803" + ], + "indented bridge of nose": [ + "HP:0011803" + ], + "abnormal muscle physiology": [ + "HP:0011804" + ], + "abnormality of muscle physiology": [ + "HP:0011804" + ], + "issue with muscle function": [ + "HP:0011804" + ], + "abnormal skeletal muscle morphology": [ + "HP:0011805" + ], + "abnormal muscle morphology": [ + "HP:0011805" + ], + "abnormality of muscle morphology": [ + "HP:0011805" + ], + "abnormally shaped muscle": [ + "HP:0011805" + ], + "issue with muscle structure": [ + "HP:0011805" + ], + "type 1 muscle fiber atrophy": [ + "HP:0011807" + ], + "type 1 muscle fibre atrophy": [ + "HP:0011807" + ], + "decrease patellar reflex": [ + "HP:0011808" + ], + "decreased patellar reflex": [ + "HP:0011808" + ], + "decrease knee jerk reflex": [ + "HP:0011808" + ], + "decreased knee jerk reflex": [ + "HP:0011808" + ], + "decreased patellar reflexes": [ + "HP:0011808" + ], + "paradoxical myotonia": [ + "HP:0011809" + ], + "impaired two - point discrimination": [ + "HP:0011810" + ], + "impaired touch localization": [ + "HP:0011811" + ], + "impaired topognosis": [ + "HP:0011811" + ], + "impaired touch localisation": [ + "HP:0011811" + ], + "agraphesthesia": [ + "HP:0011812" + ], + "increase cerebral lipofuscin": [ + "HP:0011813" + ], + "increased cerebral lipofuscin": [ + "HP:0011813" + ], + "increase urinary hypoxanthine": [ + "HP:0011814" + ], + "increased urinary hypoxanthine": [ + "HP:0011814" + ], + "cephalocele": [ + "HP:0011815" + ], + "parietal encephalocele": [ + "HP:0011816" + ], + "basal encephalocele": [ + "HP:0011817" + ], + "nasofrontal encephalocele": [ + "HP:0011818" + ], + "naso - frontal encephalocele": [ + "HP:0011818" + ], + "submucous cleft soft palate": [ + "HP:0011819" + ], + "partial thickness cleft soft palate": [ + "HP:0011819" + ], + "submucous cleft velum": [ + "HP:0011819" + ], + "membranous choanal atresia": [ + "HP:0011820" + ], + "abnormality of facial skeleton": [ + "HP:0011821" + ], + "abnormality of facial bone": [ + "HP:0011821" + ], + "abnormality of facial bones": [ + "HP:0011821" + ], + "anomaly of facial bone": [ + "HP:0011821" + ], + "anomaly of facial bones": [ + "HP:0011821" + ], + "anomaly of facial skeleton": [ + "HP:0011821" + ], + "deformity of facial skeleton": [ + "HP:0011821" + ], + "deformity of the facial bone": [ + "HP:0011821" + ], + "deformity of the facial bones": [ + "HP:0011821" + ], + "malformation of facial bone": [ + "HP:0011821" + ], + "malformation of facial bones": [ + "HP:0011821" + ], + "malformation of facial skeleton": [ + "HP:0011821" + ], + "broad chin": [ + "HP:0011822" + ], + "increase width of chin": [ + "HP:0011822" + ], + "increased width of chin": [ + "HP:0011822" + ], + "increase width of menton region": [ + "HP:0011822" + ], + "increased width of menton region": [ + "HP:0011822" + ], + "wide chin": [ + "HP:0011822" + ], + "chin with horizontal crease": [ + "HP:0011823" + ], + "chin with horizontal furrow": [ + "HP:0011823" + ], + "chin with horizontal groove": [ + "HP:0011823" + ], + "chin with horizontal sulcus": [ + "HP:0011823" + ], + "horizontal chin skin cleft": [ + "HP:0011823" + ], + "horizontal menton crease": [ + "HP:0011823" + ], + "chin with h - shape crease": [ + "HP:0011824" + ], + "chin with h - shaped crease": [ + "HP:0011824" + ], + "chin , h - shaped crease": [ + "HP:0011824" + ], + "chin , h - shape groove": [ + "HP:0011824" + ], + "chin , h - shaped groove": [ + "HP:0011824" + ], + "h - shaped dimple of the chin": [ + "HP:0011824" + ], + "tent philtrum": [ + "HP:0011825" + ], + "tented philtrum": [ + "HP:0011825" + ], + "philtrum , tent": [ + "HP:0011825" + ], + "philtrum , tented": [ + "HP:0011825" + ], + "philtrum with midline raphe": [ + "HP:0011826" + ], + "philtrum with central raphe": [ + "HP:0011826" + ], + "philtrum with midline ridge": [ + "HP:0011826" + ], + "philtrum , midline raphe": [ + "HP:0011826" + ], + "malaligned philtral ridge": [ + "HP:0011827" + ], + "malaligned philtral ridges": [ + "HP:0011827" + ], + "asymmetric philtral column": [ + "HP:0011827" + ], + "asymmetric philtral columns": [ + "HP:0011827" + ], + "asymmetric philtral ridge": [ + "HP:0011827" + ], + "asymmetric philtral ridges": [ + "HP:0011827" + ], + "malaligned philtral column": [ + "HP:0011827" + ], + "malaligned philtral columns": [ + "HP:0011827" + ], + "philtral ridge , malaligned": [ + "HP:0011827" + ], + "philtral ridges , malaligned": [ + "HP:0011827" + ], + "midline sinus of philtrum": [ + "HP:0011828" + ], + "central sinus of philtrum": [ + "HP:0011828" + ], + "philtrum , midline sinus": [ + "HP:0011828" + ], + "narrow philtrum": [ + "HP:0011829" + ], + "decrease breadth of philtrum": [ + "HP:0011829" + ], + "decreased breadth of philtrum": [ + "HP:0011829" + ], + "decrease horizontal dimension of philtrum": [ + "HP:0011829" + ], + "decreased horizontal dimension of philtrum": [ + "HP:0011829" + ], + "decreased transverse dimension of philtrum": [ + "HP:0011829" + ], + "decrease width of philtrum": [ + "HP:0011829" + ], + "decreased width of philtrum": [ + "HP:0011829" + ], + "philtrum , narrow": [ + "HP:0011829" + ], + "thin philtrum": [ + "HP:0011829" + ], + "abnormal oral mucosa morphology": [ + "HP:0011830" + ], + "abnormality of lining of mouth": [ + "HP:0011830" + ], + "abnormality of mucosa of mouth": [ + "HP:0011830" + ], + "abnormality of oral mucosa": [ + "HP:0011830" + ], + "abnormality of oral mucous membrane": [ + "HP:0011830" + ], + "deviate nasal tip": [ + "HP:0011831" + ], + "deviated nasal tip": [ + "HP:0011831" + ], + "asymmetry of nasal tip": [ + "HP:0011831" + ], + "asymmetry of tip of nose": [ + "HP:0011831" + ], + "crook nasal tip": [ + "HP:0011831" + ], + "crooked nasal tip": [ + "HP:0011831" + ], + "crooked tip of nose": [ + "HP:0011831" + ], + "deviate tip of nose": [ + "HP:0011831" + ], + "deviated tip of nose": [ + "HP:0011831" + ], + "distortion of the nasal tip": [ + "HP:0011831" + ], + "nasal tip , deviate": [ + "HP:0011831" + ], + "nasal tip , deviated": [ + "HP:0011831" + ], + "narrow nasal tip": [ + "HP:0011832" + ], + "narrow tip of nose": [ + "HP:0011832" + ], + "nasal tip , narrow": [ + "HP:0011832" + ], + "nasal tip , pinch": [ + "HP:0011832" + ], + "nasal tip , pinched": [ + "HP:0011832" + ], + "pinch nasal tip": [ + "HP:0011832" + ], + "pinched nasal tip": [ + "HP:0011832" + ], + "pinch tip of nose": [ + "HP:0011832" + ], + "pinched tip of nose": [ + "HP:0011832" + ], + "thin nasal tip": [ + "HP:0011832" + ], + "thin tip of nose": [ + "HP:0011832" + ], + "overhang nasal tip": [ + "HP:0011833" + ], + "overhanging nasal tip": [ + "HP:0011833" + ], + "droop nasal tip": [ + "HP:0011833" + ], + "drooping nasal tip": [ + "HP:0011833" + ], + "hooked tip of nose": [ + "HP:0011833" + ], + "low hang nasal tip": [ + "HP:0011833" + ], + "low hanging nasal tip": [ + "HP:0011833" + ], + "nasal tip , overhang": [ + "HP:0011833" + ], + "nasal tip , overhanging": [ + "HP:0011833" + ], + "moyamoya phenomenon": [ + "HP:0011834" + ], + "absent scaphoid": [ + "HP:0011835" + ], + "absent scaphoid bone": [ + "HP:0011835" + ], + "miss scaphoid bone": [ + "HP:0011835" + ], + "missing scaphoid bone": [ + "HP:0011835" + ], + "delay talus ossification": [ + "HP:0011836" + ], + "delayed talus ossification": [ + "HP:0011836" + ], + "partial iga deficiency": [ + "HP:0011837" + ], + "sclerodactyly": [ + "HP:0011838" + ], + "abnormal t cell count": [ + "HP:0011839" + ], + "abnormal number of t cell": [ + "HP:0011839" + ], + "abnormal number of t cells": [ + "HP:0011839" + ], + "abnormality of t cell number": [ + "HP:0011839" + ], + "abnormality of t cell physiology": [ + "HP:0011840" + ], + "ventricular flutter": [ + "HP:0011841" + ], + "abnormality of skeletal morphology": [ + "HP:0011842" + ], + "abnormally shape skeletal": [ + "HP:0011842" + ], + "abnormally shaped skeletal": [ + "HP:0011842" + ], + "abnormality of musculoskeletal physiology": [ + "HP:0011843" + ], + "abnormal appendicular skeleton morphology": [ + "HP:0011844" + ], + "short second metatarsal": [ + "HP:0011845" + ], + "short 2nd long bone of foot": [ + "HP:0011845" + ], + "osteoblastoma": [ + "HP:0011846" + ], + "giant cell tumor of bone": [ + "HP:0011847" + ], + "giant cell tumour of bone": [ + "HP:0011847" + ], + "abdominal colic": [ + "HP:0011848" + ], + "abnormal bone ossification": [ + "HP:0011849" + ], + "abnormal bone maturation": [ + "HP:0011849" + ], + "parotitis": [ + "HP:0011850" + ], + "hemopericardium": [ + "HP:0011851" + ], + "chylopericardium": [ + "HP:0011852" + ], + "serous pericardial effusion": [ + "HP:0011853" + ], + "hemoperitoneum": [ + "HP:0011854" + ], + "hematoperitoneum": [ + "HP:0011854" + ], + "pharyngeal edema": [ + "HP:0011855" + ], + "pharyngeal oedema": [ + "HP:0011855" + ], + "swell throat": [ + "HP:0011855" + ], + "swollen throat": [ + "HP:0011855" + ], + "throat swell": [ + "HP:0011855" + ], + "throat swelling": [ + "HP:0011855" + ], + "pica": [ + "HP:0011856" + ], + "plasmacytoma": [ + "HP:0011857" + ], + "reduce factor ix activity": [ + "HP:0011858" + ], + "reduced factor ix activity": [ + "HP:0011858" + ], + "low factor ix activity": [ + "HP:0011858" + ], + "punctate keratitis": [ + "HP:0011859" + ], + "metaphyseal dapple": [ + "HP:0011860" + ], + "metaphyseal dappling": [ + "HP:0011860" + ], + "dapple metaphyseal sclerosis": [ + "HP:0011860" + ], + "dappled metaphyseal sclerosis": [ + "HP:0011860" + ], + "bilateral trilobed lung": [ + "HP:0011861" + ], + "bilateral trilobed lungs": [ + "HP:0011861" + ], + "abnormal bone collagen fibril morphology": [ + "HP:0011862" + ], + "abnormal sternal ossification": [ + "HP:0011863" + ], + "abnormal maturation of breastbone": [ + "HP:0011863" + ], + "sternal ossification center abnormality": [ + "HP:0011863" + ], + "sternal ossification center abnormalities": [ + "HP:0011863" + ], + "sternal ossification centre abnormality": [ + "HP:0011863" + ], + "sternal ossification centre abnormalities": [ + "HP:0011863" + ], + "elevate plasma pyrophosphate": [ + "HP:0011864" + ], + "elevated plasma pyrophosphate": [ + "HP:0011864" + ], + "abnormal iliac wing morphology": [ + "HP:0011867" + ], + "abnormality of the wing of the ilium": [ + "HP:0011867" + ], + "sciatica": [ + "HP:0011868" + ], + "abnormal platelet function": [ + "HP:0011869" + ], + "impaired arachidonic acid - induced platelet aggregation": [ + "HP:0011870" + ], + "impaired ristocetin - induced platelet aggregation": [ + "HP:0011871" + ], + "impaired thrombin - induced platelet aggregation": [ + "HP:0011872" + ], + "abnormal platelet count": [ + "HP:0011873" + ], + "heparin - induce thrombocytopenia": [ + "HP:0011874" + ], + "heparin - induced thrombocytopenia": [ + "HP:0011874" + ], + "abnormal platelet morphology": [ + "HP:0011875" + ], + "abnormal shape of platelet": [ + "HP:0011875" + ], + "abnormal shape of platelets": [ + "HP:0011875" + ], + "abnormal platelet volume": [ + "HP:0011876" + ], + "increase mean platelet volume": [ + "HP:0011877" + ], + "increased mean platelet volume": [ + "HP:0011877" + ], + "large platelet": [ + "HP:0011877" + ], + "large platelets": [ + "HP:0011877" + ], + "abnormal platelet membrane protein expression": [ + "HP:0011878" + ], + "decrease platelet glycoprotein ib - ix - v": [ + "HP:0011879" + ], + "decreased platelet glycoprotein ib - ix - v": [ + "HP:0011879" + ], + "acute disseminate intravascular coagulation": [ + "HP:0011880" + ], + "acute disseminated intravascular coagulation": [ + "HP:0011880" + ], + "decrease platelet glycoprotein vi": [ + "HP:0011881" + ], + "decreased platelet glycoprotein vi": [ + "HP:0011881" + ], + "decrease platelet p2y12 receptor": [ + "HP:0011882" + ], + "decreased platelet p2y12 receptor": [ + "HP:0011882" + ], + "abnormal platelet granule": [ + "HP:0011883" + ], + "abnormal platelet granules": [ + "HP:0011883" + ], + "abnormal umbilical stump bleeding": [ + "HP:0011884" + ], + "hemorrhage of the eye": [ + "HP:0011885" + ], + "bleed from the eye": [ + "HP:0011885" + ], + "bleeding from the eye": [ + "HP:0011885" + ], + "haemorrhage of the eye": [ + "HP:0011885" + ], + "hyphema": [ + "HP:0011886" + ], + "choroid hemorrhage": [ + "HP:0011887" + ], + "choroid haemorrhage": [ + "HP:0011887" + ], + "choroidal haemorrhage": [ + "HP:0011887" + ], + "choroidal hemorrhage": [ + "HP:0011887" + ], + "bleed require red cell transfusion": [ + "HP:0011888" + ], + "bleeding requiring red cell transfusion": [ + "HP:0011888" + ], + "bleed with minor or no trauma": [ + "HP:0011889" + ], + "bleeding with minor or no trauma": [ + "HP:0011889" + ], + "easy bleeding": [ + "HP:0011889" + ], + "prolonged bleeding following procedure": [ + "HP:0011890" + ], + "post - partum hemorrhage": [ + "HP:0011891" + ], + "bleed post - delivery": [ + "HP:0011891" + ], + "bleeding post - delivery": [ + "HP:0011891" + ], + "post - partum haemorrhage": [ + "HP:0011891" + ], + "low level of vitamin k": [ + "HP:0011892" + ], + "low levels of vitamin k": [ + "HP:0011892" + ], + "abnormal leukocyte count": [ + "HP:0011893" + ], + "abnormal white blood cell count": [ + "HP:0011893" + ], + "impaired thromboxane a2 agonist - induced platelet aggregation": [ + "HP:0011894" + ], + "anemia due to reduced life span of red cell": [ + "HP:0011895" + ], + "anemia due to reduced life span of red cells": [ + "HP:0011895" + ], + "anaemia due to reduced life span of red cell": [ + "HP:0011895" + ], + "anaemia due to reduced life span of red cells": [ + "HP:0011895" + ], + "subconjunctival hemorrhage": [ + "HP:0011896" + ], + "subconjunctival haemorrhage": [ + "HP:0011896" + ], + "neutrophilia": [ + "HP:0011897" + ], + "increase blood neutrophil count": [ + "HP:0011897" + ], + "increased blood neutrophil counts": [ + "HP:0011897" + ], + "abnormality of circulate fibrinogen": [ + "HP:0011898" + ], + "abnormality of circulating fibrinogen": [ + "HP:0011898" + ], + "hyperfibrinogenemia": [ + "HP:0011899" + ], + "hypofibrinogenemia": [ + "HP:0011900" + ], + "low fibrinogen activity": [ + "HP:0011900" + ], + "low fibrinogen level": [ + "HP:0011900" + ], + "dysfibrinogenemia": [ + "HP:0011901" + ], + "dysfibrinogenaemia": [ + "HP:0011901" + ], + "abnormal hemoglobin": [ + "HP:0011902" + ], + "abnormal haemoglobin": [ + "HP:0011902" + ], + "abnormal hb": [ + "HP:0011902" + ], + "hbh hemoglobin": [ + "HP:0011903" + ], + "haemoglobin h": [ + "HP:0011903" + ], + "hbh haemoglobin": [ + "HP:0011903" + ], + "hemoglobin h": [ + "HP:0011903" + ], + "persistence of hemoglobin f": [ + "HP:0011904" + ], + "increase haemoglobin f": [ + "HP:0011904" + ], + "increased haemoglobin f": [ + "HP:0011904" + ], + "increase hemoglobin f": [ + "HP:0011904" + ], + "increased hemoglobin f": [ + "HP:0011904" + ], + "persistence of haemoglobin f": [ + "HP:0011904" + ], + "persistence of hbf": [ + "HP:0011904" + ], + "reduce hemoglobin a": [ + "HP:0011905" + ], + "reduced hemoglobin a": [ + "HP:0011905" + ], + "reduce haemoglobin a": [ + "HP:0011905" + ], + "reduced haemoglobin a": [ 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"abnormality of the glenoid fossa": [ + "HP:0011912" + ], + "lumbar hypertrichosis": [ + "HP:0011913" + ], + "thoracic hypertrichosis": [ + "HP:0011914" + ], + "cardiovascular calcification": [ + "HP:0011915" + ], + "toe extensor amyotrophy": [ + "HP:0011916" + ], + "short 5th toe": [ + "HP:0011917" + ], + "short fifth toe": [ + "HP:0011917" + ], + "short little toe": [ + "HP:0011917" + ], + "short pinkie toe": [ + "HP:0011917" + ], + "short pinky toe": [ + "HP:0011917" + ], + "clinodactyly of the 4th toe": [ + "HP:0011918" + ], + "4th toe clinodactyly": [ + "HP:0011918" + ], + "curvature of 4th toe": [ + "HP:0011918" + ], + "pleural empyema": [ + "HP:0011919" + ], + "pyothorax": [ + "HP:0011919" + ], + "transudative pleural effusion": [ + "HP:0011920" + ], + "exudative pleural effusion": [ + "HP:0011921" + ], + "abnormal activity of mitochondrial respiratory chain": [ + "HP:0011922" + ], + "decreased activity of mitochondrial complex i": [ + "HP:0011923" + ], + "respiratory complex i deficiency": [ + "HP:0011923" + ], + "decreased activity of mitochondrial complex iii": [ + "HP:0011924" + ], + "respiratory complex iii deficiency": [ + "HP:0011924" + ], + "decreased activity of mitochondrial atp synthase complex": [ + "HP:0011925" + ], + "respiratory complex deficiency , atpase deficiency": [ + "HP:0011925" + ], + "proximal placement of hallux": [ + "HP:0011926" + ], + "proximal placement of big toe": [ + "HP:0011926" + ], + "proximally place hallux": [ + "HP:0011926" + ], + "proximally placed halluces": [ + "HP:0011926" + ], + "short digit": [ + "HP:0011927" + ], + "very short digit": [ + "HP:0011927" + ], + "very short digits": [ + "HP:0011927" + ], + "short proximal phalanx of toe": [ + "HP:0011928" + ], + "short innermost toe bone": [ + "HP:0011928" + ], + "hypersegmentation of proximal phalanx of third finger": [ + "HP:0011929" + ], + "hyperextensible skin of chest": [ + "HP:0011930" + ], + "hyperelastic chest skin": [ + "HP:0011930" + ], + "stretchable chest skin": [ + "HP:0011930" + ], + "abnormal cerebellar peduncle morphology": [ + "HP:0011931" + ], + "abnormality of the cerebellar peduncle": [ + "HP:0011931" + ], + "abnormal superior cerebellar peduncle morphology": [ + "HP:0011932" + ], + "abnormality of the superior cerebellar peduncle": [ + "HP:0011932" + ], + "elongate superior cerebellar peduncle": [ + "HP:0011933" + ], + "elongated superior cerebellar peduncle": [ + "HP:0011933" + ], + "elongated superior cerebellar peduncles": [ + "HP:0011933" + ], + "long cerebellar peduncle": [ + "HP:0011933" + ], + "long cerebellar peduncles": [ + "HP:0011933" + ], + "dilatation of mesenteric artery": [ + "HP:0011934" + ], + "mesenteric artery aneurysm": [ + "HP:0011934" + ], + "decrease urinary urate": [ + "HP:0011935" + ], + "decreased urinary urate": [ + "HP:0011935" + ], + "decrease plasma total carnitine": [ + "HP:0011936" + ], + "decreased plasma total carnitine": [ + "HP:0011936" + ], + "hypoplastic fifth toenail": [ + "HP:0011937" + ], + "small fifth toenail": [ + "HP:0011937" + ], + "underdeveloped fifth toenail": [ + "HP:0011937" + ], + "3 - 4 finger cutaneous syndactyly": [ + "HP:0011939" + ], + "anterior wedging of t12": [ + "HP:0011940" + ], + "anterior wedging of the 12th thoracic vertebra": [ + "HP:0011940" + ], + "wedge - shape 12th thoracic vertebra": [ + "HP:0011940" + ], + "wedge - shaped 12th thoracic vertebra": [ + "HP:0011940" + ], + "anterior wedging of l2": [ + "HP:0011941" + ], + "increase urinary sulfite": [ + "HP:0011942" + ], + "increased urinary sulfite": [ + "HP:0011942" + ], + "increase urinary thiosulfate": [ + "HP:0011943" + ], + "increased urinary thiosulfate": [ + "HP:0011943" + ], + "small vessel vasculitis": [ + "HP:0011944" + ], + "bronchiolitis obliterans organize pneumonia": [ + "HP:0011945" + ], + "bronchiolitis obliterans organizing pneumonia": [ + "HP:0011945" + ], + "bronchiolitis obliterans organise pneumonia": [ + "HP:0011945" + ], + "bronchiolitis obliterans organising pneumonia": [ + "HP:0011945" + ], + "cryptogenic organise pneumonia": [ + "HP:0011945" + ], + "cryptogenic organising pneumonia": [ + "HP:0011945" + ], + "cryptogenic organize pneumonia": [ + "HP:0011945" + ], + "cryptogenic organizing pneumonia": [ + "HP:0011945" + ], + "bronchiolitis obliterans": [ + "HP:0011946" + ], + "constrictive bronchiolitis": [ + "HP:0011946" + ], + "obliterative bronchiolitis": [ + "HP:0011946" + ], + "respiratory tract infection": [ + "HP:0011947" + ], + "respiratory infection": [ + "HP:0011947" + ], + "respiratory infections": [ + "HP:0011947" + ], + "recurrent acute respiratory tract infection": [ + "HP:0011948" + ], + "acute respiratory tract infection": [ + "HP:0011948" + ], + "acute infectious pneumonia": [ + "HP:0011949" + ], + "bronchiolitis": [ + "HP:0011950" + ], + "aspiration pneumonia": [ + "HP:0011951" + ], + "acute aspiration pneumonia": [ + "HP:0011952" + ], + "pulmonary lymphoma": [ + "HP:0011953" + ], + "nodular regenerative hyperplasia of liver": [ + "HP:0011954" + ], + "nodular transformation of liver": [ + "HP:0011954" + ], + "noncirrhotic nodulation": [ + "HP:0011954" + ], + "partial nodular transformation of liver": [ + "HP:0011954" + ], + "hepatic granulomatosis": [ + "HP:0011955" + ], + "intestinal lymphoid nodular hyperplasia": [ + "HP:0011956" + ], + "abnormal pectoral muscle morphology": [ + "HP:0011957" + ], + "abnormal pec muscle": [ + "HP:0011957" + ], + "abnormal pec muscles": [ + "HP:0011957" + ], + "retinal perforation": [ + "HP:0011958" + ], + "retinal tear": [ + "HP:0011958" + ], + "torn retina": [ + "HP:0011958" + ], + "unilateral hypoplasia of pectoralis major muscle": [ + "HP:0011959" + ], + "small pec muscle on one side": [ + "HP:0011959" + ], + "underdeveloped pec muscle on one side": [ + "HP:0011959" + ], + "substantia nigra gliosis": [ + "HP:0011960" + ], + "non - obstructive azoospermia": [ + "HP:0011961" + ], + "testicular azoospermia": [ + "HP:0011961" + ], + "obstructive azoospermia": [ + "HP:0011962" + ], + "pretesticular azoospermia": [ + "HP:0011963" + ], + "intermittent painful muscle spasm": [ + "HP:0011964" + ], + "intermittent painful muscle spasms": [ + "HP:0011964" + ], + "abnormal circulate citrulline concentration": [ + "HP:0011965" + ], + "abnormal circulating citrulline concentration": [ + "HP:0011965" + ], + "elevate plasma citrulline": [ + "HP:0011966" + ], + "elevated plasma citrulline": [ + "HP:0011966" + ], + "decrease circulate copper concentration": [ + "HP:0011967" + ], + "decreased circulating copper concentration": [ + "HP:0011967" + ], + "copper deficiency": [ + "HP:0011967" + ], + "hypocupremia": [ + "HP:0011967" + ], + "reduce serum copper": [ + "HP:0011967" + ], + "reduced serum copper": [ + "HP:0011967" + ], + "feed difficulty": [ + "HP:0011968" + ], + "feeding difficulties": [ + "HP:0011968" + ], + "feeding problem": [ + "HP:0011968" + ], + "feeding problems": [ + "HP:0011968" + ], + "poor feeding": [ + "HP:0011968" + ], + "elevate circulate luteinizing hormone level": [ + "HP:0011969" + ], + "elevated circulating luteinizing hormone level": [ + "HP:0011969" + ], + "elevate lh level": [ + "HP:0011969" + ], + "elevated lh level": [ + "HP:0011969" + ], + "elevate luteinizing hormone": [ + "HP:0011969" + ], + "elevated luteinizing hormone": [ + "HP:0011969" + ], + "increase circulate luteinizing hormone level": [ + "HP:0011969" + ], + "increased circulating luteinizing hormone level": [ + "HP:0011969" + ], + "cerebral amyloid angiopathy": [ + "HP:0011970" + ], + "dermatographic urticaria": [ + "HP:0011971" + ], + "dermatographism": [ + "HP:0011971" + ], + "dermographism": [ + "HP:0011971" + ], + "skin writing": [ + "HP:0011971" + ], + "hypoglycorrhachia": [ + "HP:0011972" + ], + "decrease csf glucose": [ + "HP:0011972" + ], + "decreased csf glucose": [ + "HP:0011972" + ], + "low glucose level in cerebral spinal fluid": [ + "HP:0011972" + ], + "low glucose levels in cerebral spinal fluid": [ + "HP:0011972" + ], + "paroxysmal lethargy": [ + "HP:0011973" + ], + "myelofibrosis": [ + "HP:0011974" + ], + "aminoglycoside - induced hearing loss": [ + "HP:0011975" + ], + "elevate urinary catecholamine": [ + "HP:0011976" + ], + "elevated urinary catecholamines": [ + "HP:0011976" + ], + "elevate urinary homovanillic acid": [ + "HP:0011977" + ], + "elevated urinary homovanillic acid": [ + "HP:0011977" + ], + "increase urinary homovanillic acid": [ + "HP:0011977" + ], + "increased urinary homovanillic acid": [ + "HP:0011977" + ], + "elevate urinary vanillylmandelic acid": [ + "HP:0011978" + ], + "elevated urinary vanillylmandelic acid": [ + "HP:0011978" + ], + "increase urinary vanillylmandelic acid": [ + "HP:0011978" + ], + "increased urinary vanillylmandelic acid": [ + "HP:0011978" + ], + "elevate urinary dopamine": [ + "HP:0011979" + ], + "elevated urinary dopamine": [ + "HP:0011979" + ], + "cholesterol gallstone": [ + "HP:0011980" + ], + "cholesterol gallstones": [ + "HP:0011980" + ], + "pigment gallstone": [ + 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arch": [ + "HP:0012020" + ], + "right - sided aortic arch": [ + "HP:0012020" + ], + "persistent patent ductus venosus": [ + "HP:0012021" + ], + "congenital portosystemic venous shunt": [ + "HP:0012022" + ], + "galactosuria": [ + "HP:0012023" + ], + "increase urinary galactose level": [ + "HP:0012023" + ], + "increased urinary galactose level": [ + "HP:0012023" + ], + "hypergalactosemia": [ + "HP:0012024" + ], + "galactosemia": [ + "HP:0012024" + ], + "abnormal circulate ornithine concentration": [ + "HP:0012025" + ], + "abnormal circulating ornithine concentration": [ + "HP:0012025" + ], + "hyperornithinemia": [ + "HP:0012026" + ], + "high blood ornithine level": [ + "HP:0012026" + ], + "high blood ornithine levels": [ + "HP:0012026" + ], + "laryngeal edema": [ + "HP:0012027" + ], + "laryngeal oedema": [ + "HP:0012027" + ], + "hepatocellular adenoma": [ + "HP:0012028" + ], + "hepatic adenoma": [ + "HP:0012028" + ], + "liver cell adenoma": [ + "HP:0012028" + ], + "abnormal urine hormone 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"hyperalbuminaemia": [ + "HP:0012117" + ], + "laryngeal carcinoma": [ + "HP:0012118" + ], + "cancer of the larynx": [ + "HP:0012118" + ], + "laryngeal cancer": [ + "HP:0012118" + ], + "methemoglobinemia": [ + "HP:0012119" + ], + "methylmalonic aciduria": [ + "HP:0012120" + ], + "high blood methylmalonic acid level": [ + "HP:0012120" + ], + "high blood methylmalonic acid levels": [ + "HP:0012120" + ], + "methymalonicaciduria": [ + "HP:0012120" + ], + "panuveitis": [ + "HP:0012121" + ], + "anterior uveitis": [ + "HP:0012122" + ], + "posterior uveitis": [ + "HP:0012123" + ], + "choroiditis": [ + "HP:0012123" + ], + "intermediate uveitis": [ + "HP:0012124" + ], + "prostate cancer": [ + "HP:0012125" + ], + "prostatic cancer": [ + "HP:0012125" + ], + "stomach cancer": [ + "HP:0012126" + ], + "gastric cancer": [ + "HP:0012126" + ], + "uraciluria": [ + "HP:0012127" + ], + "high urine uracil level": [ + "HP:0012127" + ], + "high urine uracil levels": [ + "HP:0012127" + ], + "basal ganglion 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link protein glycosylation": [ + "HP:0012354" + ], + "increased fucosylation of n - linked protein glycosylation": [ + "HP:0012354" + ], + "abnormal mannosylation of n - link protein glycosylation": [ + "HP:0012355" + ], + "abnormal mannosylation of n - linked protein glycosylation": [ + "HP:0012355" + ], + "decreased mannosylation of n - link protein glycosylation": [ + "HP:0012356" + ], + "decreased mannosylation of n - linked protein glycosylation": [ + "HP:0012356" + ], + "increase mannosylation of n - link protein glycosylation": [ + "HP:0012357" + ], + "increased mannosylation of n - linked protein glycosylation": [ + "HP:0012357" + ], + "abnormal protein o - link glycosylation": [ + "HP:0012358" + ], + "abnormal protein o - linked glycosylation": [ + "HP:0012358" + ], + "abnormal fucosylation of o - link protein glycosylation": [ + "HP:0012359" + ], + "abnormal fucosylation of o - linked protein glycosylation": [ + "HP:0012359" + ], + "decreased fucosylation of o - link protein 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blood gas level": [ + "HP:0012415" + ], + "hypercapnia": [ + "HP:0012416" + ], + "high blood carbon dioxide level": [ + "HP:0012416" + ], + "hypercarbia": [ + "HP:0012416" + ], + "hypocapnia": [ + "HP:0012417" + ], + "hypocarbia": [ + "HP:0012417" + ], + "reduce carbon dioxide in the blood": [ + "HP:0012417" + ], + "reduced carbon dioxide in the blood": [ + "HP:0012417" + ], + "hypoxemia": [ + "HP:0012418" + ], + "hypoxia": [ + "HP:0012418" + ], + "low blood oxygen level": [ + "HP:0012418" + ], + "hyperoxemia": [ + "HP:0012419" + ], + "meconium stain amniotic fluid": [ + "HP:0012420" + ], + "meconium stained amniotic fluid": [ + "HP:0012420" + ], + "meconium staining of amniotic fluid": [ + "HP:0012420" + ], + "meconium - stain amniotic fluid": [ + "HP:0012420" + ], + "meconium - stained amniotic fluid": [ + "HP:0012420" + ], + "congenital absence of foreskin": [ + "HP:0012421" + ], + "absent foreskin": [ + "HP:0012421" + ], + "aposthia": [ + "HP:0012421" + ], + "villous hypertrophy of choroid plexus": [ + "HP:0012422" + ], + "choroid plexus hypertrophy": [ + "HP:0012422" + ], + "diffuse villous hypertrophy of choroid plexus": [ + "HP:0012422" + ], + "colonic inertia": [ + "HP:0012423" + ], + "chorioretinitis": [ + "HP:0012424" + ], + "stercoral ulcer": [ + "HP:0012425" + ], + "colon ulcer": [ + "HP:0012425" + ], + "recto - sigmoid colon stercoral ulcer": [ + "HP:0012425" + ], + "optic disc drusen": [ + "HP:0012426" + ], + "optic nerve head drusen": [ + "HP:0012426" + ], + "excessive femoral anteversion": [ + "HP:0012427" + ], + "prominent calcaneus": [ + "HP:0012428" + ], + "prominent heel bone": [ + "HP:0012428" + ], + "aplasia / hypoplasia of the cerebral white matter": [ + "HP:0012429" + ], + "absent / small cerebral white matter": [ + "HP:0012429" + ], + "absent / underdeveloped cerebral white matter": [ + "HP:0012429" + ], + "cerebral white matter hypoplasia": [ + "HP:0012430" + ], + "paucity of cerebral white matter": [ + "HP:0012430" + ], + "episodic fatigue": [ + "HP:0012431" + ], + "chronic fatigue": [ + "HP:0012432" + ], + "chronic extreme exhaustion": [ + "HP:0012432" + ], + "abnormal social behavior": [ + "HP:0012433" + ], + "abnormal social behaviour": [ + "HP:0012433" + ], + "abnormal social interaction": [ + "HP:0012433" + ], + "abnormal social interactions": [ + "HP:0012433" + ], + "delay social development": [ + "HP:0012434" + ], + "delayed social development": [ + "HP:0012434" + ], + "ventral shortening of foreskin": [ + "HP:0012435" + ], + "nonocclusive coronary artery atherosclerosis": [ + "HP:0012436" + ], + "non - occlusive coronary artery disease": [ + "HP:0012436" + ], + "non - occlusive coronary artery stenosis": [ + "HP:0012436" + ], + "nonocclusive coronary artery disease": [ + "HP:0012436" + ], + "nonocclusive coronary artery stenosis": [ + "HP:0012436" + ], + "abnormal gallbladder morphology": [ + "HP:0012437" + ], + "abnormal gallbladder structure": [ + "HP:0012437" + ], + "abnormal shape of gallbladder": [ + 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5 - methyltetrahydrofolate concentration": [ + "HP:0012446" + ], + "reduced csf 5 - methyltetrahydrofolate concentration": [ + "HP:0012446" + ], + "abnormal myelination": [ + "HP:0012447" + ], + "delay myelination": [ + "HP:0012448" + ], + "delayed myelination": [ + "HP:0012448" + ], + "sacroiliac joint synovitis": [ + "HP:0012449" + ], + "chronic constipation": [ + "HP:0012450" + ], + "infrequent bowel movement": [ + "HP:0012450" + ], + "infrequent bowel movements": [ + "HP:0012450" + ], + "acute constipation": [ + "HP:0012451" + ], + "restless leg": [ + "HP:0012452" + ], + "restless legs": [ + "HP:0012452" + ], + "restless legs syndrome": [ + "HP:0012452" + ], + "willis - ekbom disease": [ + "HP:0012452" + ], + "wittmaack - ekbom syndrome": [ + "HP:0012452" + ], + "bilateral wrist flexion contracture": [ + "HP:0012453" + ], + "bilateral wrist contracture": [ + "HP:0012453" + ], + "unilateral wrist flexion contracture": [ + "HP:0012454" + ], + "unilateral wrist contracture": [ + 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levels": [ + "HP:0012556" + ], + "hyperbetaalaninemia": [ + "HP:0012556" + ], + "eeg with centrotemporal focal spike wave": [ + "HP:0012557" + ], + "eeg with centrotemporal focal spike waves": [ + "HP:0012557" + ], + "abnormal t3 / t4 ratio": [ + "HP:0012558" + ], + "increase t3 / t4 ratio": [ + "HP:0012559" + ], + "increased t3 / t4 ratio": [ + "HP:0012559" + ], + "decrease t3 / t4 ratio": [ + "HP:0012560" + ], + "decreased t3 / t4 ratio": [ + "HP:0012560" + ], + "unicuspid aortic valve": [ + "HP:0012561" + ], + "premature epimetaphyseal fusion in hand": [ + "HP:0012562" + ], + "premature epimetaphyseal fusion in foot": [ + "HP:0012563" + ], + "premature epimetaphyseal fusion in tibia": [ + "HP:0012564" + ], + "premature epimetaphyseal fusion in fibula": [ + "HP:0012565" + ], + "premature epimetaphyseal fusion in radius": [ + "HP:0012566" + ], + "premature epimetaphyseal fusion in ulna": [ + "HP:0012567" + ], + "low eyelid edema": [ + "HP:0012568" + ], + "lower eyelid edema": [ + 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urolithiasis": [ + "HP:0012580" + ], + "simple renal cyst": [ + "HP:0012581" + ], + "simple kidney cyst": [ + "HP:0012581" + ], + "solitary renal cyst": [ + "HP:0012581" + ], + "bilateral renal dysplasia": [ + "HP:0012582" + ], + "unilateral renal hypoplasia": [ + "HP:0012583" + ], + "small kidney on one side": [ + "HP:0012583" + ], + "underdeveloped kidney on one side": [ + "HP:0012583" + ], + "bilateral renal hypoplasia": [ + "HP:0012584" + ], + "renal atrophy": [ + "HP:0012585" + ], + "kidney degeneration": [ + "HP:0012585" + ], + "bilateral renal atrophy": [ + "HP:0012586" + ], + "bilateral kidney degeneration": [ + "HP:0012586" + ], + "macroscopic hematuria": [ + "HP:0012587" + ], + "bloody urine": [ + "HP:0012587" + ], + "gross hematuria": [ + "HP:0012587" + ], + "steroid - resistant nephrotic syndrome": [ + "HP:0012588" + ], + "multidrug - resistant nephrotic syndrome": [ + "HP:0012589" + ], + "abnormal urine output": [ + "HP:0012590" + ], + "abnormal urinary electrolyte concentration": [ + "HP:0012591" + ], + "urinary electrolyte imbalance": [ + "HP:0012591" + ], + "albuminuria": [ + "HP:0012592" + ], + "nephrotic range proteinuria": [ + "HP:0012593" + ], + "moderate albuminuria": [ + "HP:0012594" + ], + "high urine albumin level": [ + "HP:0012594" + ], + "high urine albumin levels": [ + "HP:0012594" + ], + "microalbuminuria": [ + "HP:0012594" + ], + "mild proteinuria": [ + "HP:0012595" + ], + "moderate proteinuria": [ + "HP:0012596" + ], + "heavy proteinuria": [ + "HP:0012597" + ], + "severly high blood protein level": [ + "HP:0012597" + ], + "severly high blood protein levels": [ + "HP:0012597" + ], + "abnormal urine potassium concentration": [ + "HP:0012598" + ], + "abnormal urine k concentration": [ + "HP:0012598" + ], + "abnormal urine phosphate concentration": [ + "HP:0012599" + ], + "abnormal urine chloride concentration": [ + "HP:0012600" + ], + "abnormal urine cl concentration": [ + "HP:0012600" + ], + "abnormal urine cl - concentration": [ + 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sodium": [ + "HP:0012605" + ], + "renal sodium wasting": [ + "HP:0012606" + ], + "kidney sodium wasting": [ + "HP:0012606" + ], + "renal na waste": [ + "HP:0012606" + ], + "renal na wasting": [ + "HP:0012606" + ], + "renal na+ wasting": [ + "HP:0012606" + ], + "abnormal urine magnesium concentration": [ + "HP:0012607" + ], + "hypermagnesiuria": [ + "HP:0012608" + ], + "hypomagnesiuria": [ + "HP:0012609" + ], + "decrease urine magnesium": [ + "HP:0012609" + ], + "decreased urine magnesium": [ + "HP:0012609" + ], + "low urine magnesium level": [ + "HP:0012609" + ], + "low urine magnesium levels": [ + "HP:0012609" + ], + "abnormality of urinary uric acid concentration": [ + "HP:0012610" + ], + "increase urinary urate": [ + "HP:0012611" + ], + "increased urinary urate": [ + "HP:0012611" + ], + "abnormal urinary sulfate concentration": [ + "HP:0012612" + ], + "abnormal urinary sulphate concentration": [ + "HP:0012612" + ], + "increase urinary sulfate": [ + "HP:0012613" + ], + "increased 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"HP:0012815" + ], + "right ventricular noncompaction cardiomyopathy": [ + "HP:0012816" + ], + "noncompaction cardiomyopathy": [ + "HP:0012817" + ], + "noncompaction of the ventricular myocardium": [ + "HP:0012817" + ], + "spongiform cardiomyopathy": [ + "HP:0012817" + ], + "biventricular noncompaction cardiomyopathy": [ + "HP:0012818" + ], + "myocarditis": [ + "HP:0012819" + ], + "inflammation of heart muscle": [ + "HP:0012819" + ], + "bilateral vocal cord paralysis": [ + "HP:0012820" + ], + "unilateral vocal cord paresis": [ + "HP:0012821" + ], + "bilateral vocal cord paresis": [ + "HP:0012822" + ], + "clinical modifier": [ + "HP:0012823" + ], + "phenotypic modifier": [ + "HP:0012823" + ], + "severity": [ + "HP:0012824" + ], + "intensity": [ + "HP:0012824" + ], + "mild": [ + "HP:0012825" + ], + "moderate": [ + "HP:0012826" + ], + "borderline": [ + "HP:0012827" + ], + "severe": [ + "HP:0012828" + ], + "profound": [ + "HP:0012829" + ], + "position": [ + "HP:0012830" + ], + "laterality": 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intestinal hemorrhage": [ + "HP:0012849" + ], + "small intestinal dysmotility": [ + "HP:0012850" + ], + "colonic stenosis": [ + "HP:0012851" + ], + "narrowing of the colon": [ + "HP:0012851" + ], + "stenosis of the colon": [ + "HP:0012851" + ], + "hepatic bridging fibrosis": [ + "HP:0012852" + ], + "scrotal hypospadias": [ + "HP:0012853" + ], + "midshaft hypospadias": [ + "HP:0012854" + ], + "scrotal hyperpigmentation": [ + "HP:0012855" + ], + "hyperpigmentation of the scrotum": [ + "HP:0012855" + ], + "hyperpigmented scrotum": [ + "HP:0012855" + ], + "increase pigmentation in scrotum": [ + "HP:0012855" + ], + "increased pigmentation in scrotum": [ + "HP:0012855" + ], + "abnormal scrotal rugation": [ + "HP:0012856" + ], + "increase scrotal rugation": [ + "HP:0012857" + ], + "increased scrotal rugation": [ + "HP:0012857" + ], + "decrease scrotal rugation": [ + "HP:0012858" + ], + "decreased scrotal rugation": [ + "HP:0012858" + ], + "esophageal leukoplakia": [ + "HP:0012859" + ], + "esophageal epidermoid metaplasia": [ + "HP:0012859" + ], + "testicular fibrosis": [ + "HP:0012860" + ], + "fibrotic testis": [ + "HP:0012860" + ], + "fibrotic testes": [ + "HP:0012860" + ], + "fibrotic testicle": [ + "HP:0012860" + ], + "ovotestis": [ + "HP:0012861" + ], + "abnormal germ cell morphology": [ + "HP:0012862" + ], + "abnormal shape of a reproductive cell": [ + "HP:0012862" + ], + "abnormally shaped germ cell": [ + "HP:0012862" + ], + "abnormally shaped reproductive cell": [ + "HP:0012862" + ], + "abnormal male germ cell morphology": [ + "HP:0012863" + ], + "abnormal sperm morphology": [ + "HP:0012864" + ], + "abnormal shape of sperm": [ + "HP:0012864" + ], + "teratospermia": [ + "HP:0012864" + ], + "teratozoospermia": [ + "HP:0012864" + ], + "abnormal sperm head morphology": [ + "HP:0012865" + ], + "sperm head anomaly": [ + "HP:0012865" + ], + "abnormal sperm neck morphology": [ + "HP:0012866" + ], + "sperm neck anomaly": [ + "HP:0012866" + ], + "abnormal sperm mid - 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system physiology": [ + "HP:0012874" + ], + "abnormal male genital system physiology": [ + "HP:0012874" + ], + "abnormal ejaculation": [ + "HP:0012875" + ], + "premature ejaculation": [ + "HP:0012876" + ], + "retrograde ejaculation": [ + "HP:0012877" + ], + "retard ejaculation": [ + "HP:0012878" + ], + "retarded ejaculation": [ + "HP:0012878" + ], + "delay ejaculation": [ + "HP:0012878" + ], + "delayed ejaculation": [ + "HP:0012878" + ], + "anejaculation": [ + "HP:0012879" + ], + "ejaculatory incompetence": [ + "HP:0012879" + ], + "abnormal labium minora morphology": [ + "HP:0012880" + ], + "abnormal labia minora morphology": [ + "HP:0012880" + ], + "abnormality of the inner vaginal lip": [ + "HP:0012880" + ], + "abnormality of the inner vaginal lips": [ + "HP:0012880" + ], + "abnormality of the labium minora": [ + "HP:0012880" + ], + "abnormality of the labia minora": [ + "HP:0012880" + ], + "abnormal labium majora morphology": [ + "HP:0012881" + ], + "abnormal labia majora 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count": [ + "HP:0020058" + ], + "increase red blood cell count": [ + "HP:0020059" + ], + "increased red blood cell count": [ + "HP:0020059" + ], + "increase rbc count": [ + "HP:0020059" + ], + "increased rbc count": [ + "HP:0020059" + ], + "decrease red blood cell count": [ + "HP:0020060" + ], + "decreased red blood cell count": [ + "HP:0020060" + ], + "decrease rbc count": [ + "HP:0020060" + ], + "decreased rbc count": [ + "HP:0020060" + ], + "abnormal hemoglobin concentration": [ + "HP:0020061" + ], + "abnormal haemoglobin concentration": [ + "HP:0020061" + ], + "abnormal hb concentration": [ + "HP:0020061" + ], + "decrease hemoglobin concentration": [ + "HP:0020062" + ], + "decreased hemoglobin concentration": [ + "HP:0020062" + ], + "decrease haemoglobin concentration": [ + "HP:0020062" + ], + "decreased haemoglobin concentration": [ + "HP:0020062" + ], + "decrease hb concentration": [ + "HP:0020062" + ], + "decreased hb concentration": [ + "HP:0020062" + ], + "increase hemoglobin 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inclusion bodies": [ + "HP:0020080" + ], + "pappenheimer body": [ + "HP:0020081" + ], + "pappenheimer bodies": [ + "HP:0020081" + ], + "heinz body": [ + "HP:0020082" + ], + "heinz bodies": [ + "HP:0020082" + ], + "furuncle": [ + "HP:0020083" + ], + "boil": [ + "HP:0020083" + ], + "carbuncle": [ + "HP:0020084" + ], + "infection follow live vaccination": [ + "HP:0020085" + ], + "infection following live vaccination": [ + "HP:0020085" + ], + "bcgitis": [ + "HP:0020086" + ], + "bcgosis": [ + "HP:0020087" + ], + "bcgiosis": [ + "HP:0020087" + ], + "disseminate bacillus calmette - guerin infection": [ + "HP:0020087" + ], + "disseminated bacillus calmette - guerin infection": [ + "HP:0020087" + ], + "post - vaccination measles": [ + "HP:0020088" + ], + "vaccine associate measles": [ + "HP:0020088" + ], + "vaccine associated measles": [ + "HP:0020088" + ], + "post - vaccination rubella": [ + "HP:0020089" + ], + "post - vaccination polio": [ + "HP:0020090" + ], + "post - vaccination rotavirus 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"abnormal cd4+cd25+ regulatory t cell proportion": [ + "HP:0020111" + ], + "abnormal cd4+cd25+ treg cell proportion": [ + "HP:0020111" + ], + "increase proportion of cd4+cd25+ regulatory t cell": [ + "HP:0020112" + ], + "increased proportion of cd4+cd25+ regulatory t cells": [ + "HP:0020112" + ], + "elevate proportion of cd4+cd25+ regulatory t cell": [ + "HP:0020112" + ], + "elevated proportion of cd4+cd25+ regulatory t cells": [ + "HP:0020112" + ], + "increase proportion of cd4+cd25+ treg cell": [ + "HP:0020112" + ], + "increased proportion of cd4+cd25+ treg cells": [ + "HP:0020112" + ], + "decreased proportion of cd4+cd25+ regulatory t cell": [ + "HP:0020113" + ], + "decreased proportion of cd4+cd25+ regulatory t cells": [ + "HP:0020113" + ], + "decreased proportion of cd4+cd25+ treg cell": [ + "HP:0020113" + ], + "decreased proportion of cd4+cd25+ treg cells": [ + "HP:0020113" + ], + "reduce proportion of cd4+cd25+ regulatory t cell": [ + "HP:0020113" + ], + "reduced proportion of cd4+cd25+ regulatory t cells": [ + "HP:0020113" + ], + "persistent human papillomavirus infection": [ + "HP:0020114" + ], + "hypoplastic dermoepidermal hemidesmosomes": [ + "HP:0020117" + ], + "radial artery aplasia": [ + "HP:0020118" + ], + "abnormal retinal nerve fiber layer morphology": [ + "HP:0020119" + ], + "abnormal retinal nerve fibre layer morphology": [ + "HP:0020119" + ], + "retinal nerve fiber edema": [ + "HP:0020120" + ], + "retinal nerve fibre oedema": [ + "HP:0020120" + ], + "conception by assisted reproductive technology": [ + "HP:0020121" + ], + "bite cell": [ + "HP:0020122" + ], + "bite cells": [ + "HP:0020122" + ], + "blister cell": [ + "HP:0020122" + ], + "blister cells": [ + "HP:0020122" + ], + "degmacytes": [ + "HP:0020122" + ], + "tympanosclerosis": [ + "HP:0020123" + ], + "tympanic calcification": [ + "HP:0020123" + ], + "spontaneous conjunctival filter bleb": [ + "HP:0020125" + ], + "spontaneous conjunctival filtering bleb": [ + "HP:0020125" + ], + 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natriuretic peptide level": [ + "HP:0020182" + ], + "increase circulate a - type natriuretic peptide level": [ + "HP:0020183" + ], + "increased circulating a - type natriuretic peptide level": [ + "HP:0020183" + ], + "decrease circulate a - type natriuretic peptide level": [ + "HP:0020184" + ], + "decreased circulating a - type natriuretic peptide level": [ + "HP:0020184" + ], + "superior cerebellar dysplasia": [ + "HP:0020185" + ], + "multilobulated spleen": [ + "HP:0020186" + ], + "multi - lobulated spleen": [ + "HP:0020186" + ], + "thick pachygyria": [ + "HP:0020187" + ], + "pachygyria with cortical thickness > 10 mm": [ + "HP:0020187" + ], + "pachygyria with cortical thickness above 10 mm": [ + "HP:0020187" + ], + "anterior predominant pachygyria with 5 - 10 mm cortical thickness": [ + "HP:0020188" + ], + "posterior predominant thick cortex pachygyria": [ + "HP:0020189" + ], + "occipital predomimant classic pachygyria": [ + "HP:0020189" + ], + "pachygyria with cortical thickness 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organism": [ + "HP:0020204" + ], + "renal tubulointerstitial bacterial organisms": [ + "HP:0020204" + ], + "tubulointerstitial fungal infiltration": [ + "HP:0020205" + ], + "renal tubulointerstitial fungal organism": [ + "HP:0020205" + ], + "renal tubulointerstitial fungal organisms": [ + "HP:0020205" + ], + "simple ear": [ + "HP:0020206" + ], + "reflex seizure": [ + "HP:0020207" + ], + "eat - induced seizure": [ + "HP:0020208" + ], + "eating - induced seizure": [ + "HP:0020208" + ], + "hot water - induced seizure": [ + "HP:0020209" + ], + "praxis - induced seizure": [ + "HP:0020210" + ], + "proprioceptive - induced seizure": [ + "HP:0020211" + ], + "read - induced seizure": [ + "HP:0020212" + ], + "reading - induced seizure": [ + "HP:0020212" + ], + "somatosensory - induced seizure": [ + "HP:0020213" + ], + "startle - induced seizure": [ + "HP:0020214" + ], + "think - induced seizure": [ + "HP:0020215" + ], + "thinking - induced seizure": [ + "HP:0020215" + ], + "cognition induce 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"quelprud nodule": [ + "HP:0030023" + ], + "pretragal ectopia": [ + "HP:0030024" + ], + "accessory tragus": [ + "HP:0030024" + ], + "extra cartilage in front of the ear": [ + "HP:0030024" + ], + "pretragal duplication": [ + "HP:0030024" + ], + "auricular pit": [ + "HP:0030025" + ], + "square superior portion of helix": [ + "HP:0030026" + ], + "squared superior portion of helix": [ + "HP:0030026" + ], + "abnormality of the nasal cartilage": [ + "HP:0030027" + ], + "abnormality of cartilage of nose": [ + "HP:0030027" + ], + "anomaly of cartilage of nose": [ + "HP:0030027" + ], + "anomaly of nasal cartilage": [ + "HP:0030027" + ], + "deformity of cartilage of nose": [ + "HP:0030027" + ], + "deformity of nasal cartilage": [ + "HP:0030027" + ], + "malformation of cartilage of nose": [ + "HP:0030027" + ], + "malformation of nasal cartilage": [ + "HP:0030027" + ], + "absent nasal cartilage": [ + "HP:0030028" + ], + "absent cartilage of nose": [ + "HP:0030028" + ], + "agenesis of cartilage of 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adenosine deaminase level": [ + "HP:0030270" + ], + "elevated red cell adenosine deaminase level": [ + "HP:0030270" + ], + "reduce erythrocyte 2,3 - diphosphoglycerate concentration": [ + "HP:0030271" + ], + "reduced erythrocyte 2,3 - diphosphoglycerate concentration": [ + "HP:0030271" + ], + "abnormal erythrocyte enzyme level": [ + "HP:0030272" + ], + "reduce red cell adenosine deaminase level": [ + "HP:0030273" + ], + "reduced red cell adenosine deaminase level": [ + "HP:0030273" + ], + "accessory scrotum": [ + "HP:0030274" + ], + "extra scrotum": [ + "HP:0030274" + ], + "ectopic scrotum": [ + "HP:0030275" + ], + "abnormal scrotum position": [ + "HP:0030275" + ], + "small scrotum": [ + "HP:0030276" + ], + "underdeveloped scrotum": [ + "HP:0030276" + ], + "abnormal vertebral pedicle morphology": [ + "HP:0030277" + ], + "hypoplastic vertebral pedicle": [ + "HP:0030278" + ], + "hypoplastic l5 vertebral pedicle": [ + "HP:0030279" + ], + "rib gap": [ + "HP:0030280" + ], + "cervical c3 / c4 vertebral fusion": [ + "HP:0030281" + ], + "posterior rib gap": [ + "HP:0030282" + ], + "dorsal rib defect": [ + "HP:0030282" + ], + "partial absence of the septum pellucidum": [ + "HP:0030283" + ], + "triangular tongue": [ + "HP:0030284" + ], + "triangle shape tongue": [ + "HP:0030284" + ], + "triangle shaped tongue": [ + "HP:0030284" + ], + "splay superior cerebellar peduncle": [ + "HP:0030285" + ], + "splayed superior cerebellar peduncle": [ + "HP:0030285" + ], + "atrophic superior cerebellar peduncle": [ + "HP:0030286" + ], + "flatten femoral epiphysis": [ + "HP:0030289" + ], + "flattened femoral epiphysis": [ + "HP:0030289" + ], + "flattended end part of thigh bone": [ + "HP:0030289" + ], + "unossified sacrum": [ + "HP:0030290" + ], + "absence of sacrum ossification": [ + "HP:0030290" + ], + "low - limb metaphyseal irregularity": [ + "HP:0030291" + ], + "lower - limb metaphyseal irregularity": [ + "HP:0030291" + ], + "tibial metaphyseal irregularity": [ + "HP:0030292" + ], + "fibular metaphyseal irregularity": [ + "HP:0030293" + ], + "irregularity of wide portion of calf bone": [ + "HP:0030293" + ], + "metaphyseal chondromatosis of tibia": [ + "HP:0030294" + ], + "metaphyseal chondromatosis of femur": [ + "HP:0030295" + ], + "metaphyseal chondromatosis of radius": [ + "HP:0030296" + ], + "metaphyseal chondromatosis of ulna": [ + "HP:0030297" + ], + "metaphyseal chondromatosis of humerus": [ + "HP:0030298" + ], + "distal femoral metaphyseal abnormality": [ + "HP:0030299" + ], + "abnormality of wide portion of outermost thighbone": [ + "HP:0030299" + ], + "10 pair of rib": [ + "HP:0030300" + ], + "10 pairs of ribs": [ + "HP:0030300" + ], + "abnormality of the anterior commissure": [ + "HP:0030301" + ], + "agenesis of the anterior commissure": [ + "HP:0030302" + ], + "hypoplastic anterior commissure": [ + "HP:0030303" + ], + "abnormal number of vertebra": [ + "HP:0030304" + ], + "abnormal number of vertebrae": [ + "HP:0030304" + ], + "decreased number of vertebra": [ + "HP:0030305" + ], + "decreased number of vertebrae": [ + "HP:0030305" + ], + "11 thoracic vertebra": [ + "HP:0030306" + ], + "11 thoracic vertebrae": [ + "HP:0030306" + ], + "flare low limb metaphysis": [ + "HP:0030307" + ], + "flared lower limb metaphysis": [ + "HP:0030307" + ], + "flared metaphysis of low limb bone": [ + "HP:0030307" + ], + "flared metaphysis of lower limb bone": [ + "HP:0030307" + ], + "flare distal tibial metaphysis": [ + "HP:0030308" + ], + "flared distal tibial metaphysis": [ + "HP:0030308" + ], + "flare outermost metaphysis of shankbone": [ + "HP:0030308" + ], + "flared outermost metaphysis of shankbone": [ + "HP:0030308" + ], + "flare outermost metaphysis of shinbone": [ + "HP:0030308" + ], + "flared outermost metaphysis of shinbone": [ + "HP:0030308" + ], + "flare distal fibular metaphysis": [ + "HP:0030309" + ], + "flared distal fibular metaphysis": [ + "HP:0030309" + ], + "flare outermost wide portion of of calf bone": [ + "HP:0030309" + ], + 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vertebral artery morphology": [ + "HP:0030321" + ], + "abnormality of the vertebral artery": [ + "HP:0030321" + ], + "vertebral artery hypoplasia": [ + "HP:0030322" + ], + "unilateral vertebral artery hypoplasia": [ + "HP:0030323" + ], + "bilateral vertebral artery hypoplasia": [ + "HP:0030324" + ], + "cervicomedullary schisis": [ + "HP:0030325" + ], + "abnormal macrophage count": [ + "HP:0030326" + ], + "abnormal osteoclast count": [ + "HP:0030327" + ], + "decrease osteoclast count": [ + "HP:0030328" + ], + "decreased osteoclast count": [ + "HP:0030328" + ], + "retinal thinning": [ + "HP:0030329" + ], + "multinucleated giant chondrocytes in epiphyseal cartilage": [ + "HP:0030330" + ], + "impaired stimulus - induced skin wrinkling": [ + "HP:0030331" + ], + "obsolete abnormal t cell morphology": [ + "HP:0030332" + ], + "abnormal alpha - beta t cell morphology": [ + "HP:0030333" + ], + "abnormal cd4 - positive , cd25 - positive , alpha - beta regulatory t cell morphology": [ + "HP:0030334" + ], + "abnormal cd4 - positive , cd25 - positive , alpha - beta regulatory t cell count": [ + "HP:0030335" + ], + "absence of cd4 - positive , cd25 - positive regulatory t cell": [ + "HP:0030336" + ], + "absence of cd4 - positive , cd25 - positive regulatory t cells": [ + "HP:0030336" + ], + "absence of cd4+cd25+ t regulatory cell": [ + "HP:0030336" + ], + "absence of cd4+cd25+ t regulatory cells": [ + "HP:0030336" + ], + "absence of cd4+cd25+ tregs": [ + "HP:0030336" + ], + "elevate cd4 - positive , cd25 - positive regulatory t cell count": [ + "HP:0030337" + ], + "elevated cd4 - positive , cd25 - positive regulatory t cell count": [ + "HP:0030337" + ], + "abnormal circulate gonadotropin concentration": [ + "HP:0030338" + ], + "abnormal circulating gonadotropin concentration": [ + "HP:0030338" + ], + "abnormal circulate gonadotropin level": [ + "HP:0030338" + ], + "abnormal circulating gonadotropin level": [ + "HP:0030338" + ], + "decrease circulate gonadotropin concentration": [ + "HP:0030339" + ], + "decreased circulating gonadotropin concentration": [ + "HP:0030339" + ], + "decrease circulate gonadotropin level": [ + "HP:0030339" + ], + "decreased circulating gonadotropin level": [ + "HP:0030339" + ], + "obsolete increase circulate gonadotropin level": [ + "HP:0030340" + ], + "obsolete increased circulating gonadotropin level": [ + "HP:0030340" + ], + "decrease circulate follicle stimulate hormone concentration": [ + "HP:0030341" + ], + "decreased circulating follicle stimulating hormone concentration": [ + "HP:0030341" + ], + "decrease circulate follicle stimulate hormone level": [ + "HP:0030341" + ], + "decreased circulating follicle stimulating hormone level": [ + "HP:0030341" + ], + "decrease circulate luteinizing hormone level": [ + "HP:0030344" + ], + "decreased circulating luteinizing hormone level": [ + "HP:0030344" + ], + "decrease circulate luteinising hormone level": [ + "HP:0030344" + ], + "decreased circulating luteinising hormone level": [ + "HP:0030344" + ], + "abnormal circulate luteinizing hormone concentration": [ + "HP:0030345" + ], + "abnormal circulating luteinizing hormone concentration": [ + "HP:0030345" + ], + "abnormal circulate luteinizing hormone level": [ + "HP:0030345" + ], + "abnormal circulating luteinizing hormone level": [ + "HP:0030345" + ], + "abnormal luteinizing hormone level": [ + "HP:0030345" + ], + "increase circulating lutropin": [ + "HP:0030345" + ], + "increased circulating lutropin": [ + "HP:0030345" + ], + "abnormal circulate follicle - stimulate hormone concentration": [ + "HP:0030346" + ], + "abnormal circulating follicle - stimulating hormone concentration": [ + "HP:0030346" + ], + "abnormal circulate follicle - stimulate hormone level": [ + "HP:0030346" + ], + "abnormal circulating follicle - stimulating hormone level": [ + "HP:0030346" + ], + "abnormal circulate androgen level": [ + "HP:0030347" + ], + "abnormal circulating androgen level": [ + "HP:0030347" + ], + "increase circulate androgen concentration": [ + "HP:0030348" + ], + "increased circulating androgen concentration": [ + "HP:0030348" + ], + "increase circulate androgen level": [ + "HP:0030348" + ], + "increased circulating androgen level": [ + "HP:0030348" + ], + "decrease circulate androgen concentration": [ + "HP:0030349" + ], + "decreased circulating androgen concentration": [ + "HP:0030349" + ], + "decrease circulate androgen level": [ + "HP:0030349" + ], + "decreased circulating androgen level": [ + "HP:0030349" + ], + "erythematous papule": [ + "HP:0030350" + ], + "red - blue papule": [ + "HP:0030350" + ], + "urticarial plaque": [ + "HP:0030351" + ], + "abnormal serum insulin - like growth factor 1 level": [ + "HP:0030352" + ], + "decrease serum insulin - like growth factor 1": [ + "HP:0030353" + ], + "decreased serum insulin - like growth factor 1": [ + "HP:0030353" + ], + "abnormal serum interferon level": [ + "HP:0030354" + ], + "abnormal serum interferon - gamma level": [ + "HP:0030355" + ], + "increase serum interferon - gamma level": [ + "HP:0030356" + ], + "increased serum interferon - gamma level": [ + "HP:0030356" + ], + "small cell lung carcinoma": [ + "HP:0030357" + ], + "oat cell carcinoma of lung": [ + "HP:0030357" + ], + "oat cell lung cancer": [ + "HP:0030357" + ], + "small cell lung cancer": [ + "HP:0030357" + ], + "non - small cell lung carcinoma": [ + "HP:0030358" + ], + "non - small cell lung cancer": [ + "HP:0030358" + ], + "squamous cell lung carcinoma": [ + "HP:0030359" + ], + "large cell lung carcinoma": [ + "HP:0030360" + ], + "abnormal circulate eicosanoid concentration": [ + "HP:0030361" + ], + "abnormal circulating eicosanoid concentration": [ + "HP:0030361" + ], + "abnormality of icosanoid metabolism": [ + "HP:0030361" + ], + "reduce muscle carnitine level": [ + "HP:0030362" + ], + "reduced muscle carnitine level": [ + "HP:0030362" + ], + "primary caesarian section": [ + "HP:0030363" + ], + "secondary caesarian section": [ + "HP:0030364" + ], + "vaginal birth after caesarian": [ + "HP:0030365" + ], + "delivery by odon device": [ + "HP:0030366" + ], + "finger hyperphalangy": [ + "HP:0030367" + ], + "hyperphalangy of the 2nd finger": [ + "HP:0030368" + ], + "hyperphalangy of index finger": [ + "HP:0030368" + ], + "induced vaginal delivery": [ + "HP:0030369" + ], + "abnormal proportion of naive b cell": [ + "HP:0030370" + ], + "abnormal proportion of naive b cells": [ + "HP:0030370" + ], + "increase proportion of naive b cell": [ + "HP:0030371" + ], + "increased proportion of naive b cells": [ + "HP:0030371" + ], + "decreased proportion of naive b cell": [ + "HP:0030372" + ], + "decreased proportion of naive b cells": [ + "HP:0030372" + ], + "abnormal proportion of memory b cell": [ + "HP:0030373" + ], + "abnormal proportion of memory b cells": [ + "HP:0030373" + ], + "decreased proportion of memory b cell": [ + "HP:0030374" + ], + "decreased proportion of memory b cells": [ + "HP:0030374" + ], + "increase proportion of memory b cell": [ + "HP:0030375" + ], + "increased proportion of memory b cells": [ + "HP:0030375" + ], + "abnormal proportion of immature b cell": [ + "HP:0030376" + ], + "abnormal proportion of immature b cells": [ + "HP:0030376" + ], + "abnormal proportion of cd19+ / cd21low b cell": [ + "HP:0030376" + ], + "abnormal proportion of cd19+ / cd21low b cells": [ + "HP:0030376" + ], + "increase proportion of immature b cell": [ + "HP:0030377" + ], + "increased proportion of immature b cells": [ + "HP:0030377" + ], + "increase proportion of cd19+ / cd21low b cell": [ + "HP:0030377" + ], + "increased proportion of cd19+ / cd21low b cells": [ + "HP:0030377" + ], + "decreased proportion of immature b cell": [ + "HP:0030378" + ], + "decreased proportion of immature b cells": [ + "HP:0030378" + ], + "decreased proportion of cd19+ / cd21low b cell": [ + "HP:0030378" + ], + "decreased proportion of cd19+ / cd21low b cells": [ + "HP:0030378" + ], + "abnormal proportion of transitional b cell": [ + "HP:0030379" + ], + "abnormal proportion of transitional b cells": [ + "HP:0030379" + ], + "abnormal proportion of cd19+cd38+igm+ cell": [ + "HP:0030379" + ], + "abnormal proportion of cd19+cd38+igm+ cells": [ + "HP:0030379" + ], + "decreased proportion of transitional b cell": [ + "HP:0030380" + ], + "decreased proportion of transitional b cells": [ + "HP:0030380" + ], + "decreased proportion of cd19+cd38+igm+ cell": [ + "HP:0030380" + ], + "decreased proportion of cd19+cd38+igm+ cells": [ + "HP:0030380" + ], + "increase proportion of transitional b cell": [ + "HP:0030381" + ], + "increased proportion of transitional b cells": [ + "HP:0030381" + ], + "increase proportion of cd19+cd38+igm+ cell": [ + "HP:0030381" + ], + "increased proportion of cd19+cd38+igm+ cells": [ + "HP:0030381" + ], + "abnormal proportion of marginal zone b cell": [ + "HP:0030383" + ], + "abnormal proportion of marginal zone b cells": [ + "HP:0030383" + ], + "decreased proportion of marginal zone b cell": [ + "HP:0030384" + ], + "decreased proportion of marginal zone b cells": [ + "HP:0030384" + ], + "increase proportion of marginal zone b cell": [ + "HP:0030385" + ], + "increased proportion of marginal zone b cells": [ + "HP:0030385" + ], + "abnormal proportion of class - switched memory b cell": [ + "HP:0030386" + ], + "abnormal proportion of class - switched memory b cells": [ + "HP:0030386" + ], + "abnormal proportion of cd19+cd27+igd - cell": [ + "HP:0030386" + ], + "abnormal proportion of cd19+cd27+igd - cells": [ + "HP:0030386" + ], + "increase proportion of class - switched memory b cell": [ + "HP:0030387" + ], + "increased proportion of class - switched memory b cells": [ + "HP:0030387" + ], + "increase proportion of cd19+cd27+igd - cell": [ + "HP:0030387" + ], + "increased proportion of cd19+cd27+igd - cells": [ + "HP:0030387" + ], + "decreased proportion of class - switched memory b cell": [ + "HP:0030388" + ], + "decreased proportion of class - switched memory b cells": [ + "HP:0030388" + ], + "decreased proportion of cd19+cd27+igd - cell": [ + "HP:0030388" + ], + "decreased proportion of cd19+cd27+igd - cells": [ + "HP:0030388" + ], + "abnormal circulate thromboxane concentration": [ + "HP:0030389" + ], + "abnormal circulating thromboxane concentration": [ + "HP:0030389" + ], + "reduce circulate leukotriene c4 concentration": [ + "HP:0030390" + ], + "reduced circulating leukotriene c4 concentration": [ + "HP:0030390" + ], + "speak word recognition deficit": [ + "HP:0030391" + ], + "spoken word recognition deficit": [ + "HP:0030391" + ], + "choroid plexus carcinoma": [ + "HP:0030392" + ], + "endolymphatic sac tumor": [ + "HP:0030393" + ], + "aggressive papillary middle ear tumor": [ + "HP:0030393" + ], + "aggressive papillary middle ear tumour": [ + "HP:0030393" + ], + "endolymphatic sac tumour": [ + "HP:0030393" + ], + "heffner tumor": [ + "HP:0030393" + ], + "heffner tumour": [ + "HP:0030393" + ], + "low - grade adenocarcinoma of endolymphatic sac origin": [ + "HP:0030393" + ], + "fallopian tube carcinoma": [ + "HP:0030394" + ], + "abnormal platelet granule secretion": [ + "HP:0030396" + ], + "abnormal platelet dense granule secretion": [ + "HP:0030397" + ], + "abnormal platelet atp dense granule secretion": [ + "HP:0030398" + ], + "abnormal platelet alpha granule secretion": [ + "HP:0030399" + ], + "abnormal platelet lysosome secretion": [ + "HP:0030400" + ], + "abnormal platelet dense granule atp / adp ratio": [ + "HP:0030401" + ], + "abnormal platelet aggregation": [ + "HP:0030402" + ], + "spontaneous platelet aggregation": [ + "HP:0030403" + ], + "glucagonoma": [ + "HP:0030404" + ], + "pancreatic endocrine tumor": [ + "HP:0030405" + ], + "pancreatic endocrine tumour": [ + "HP:0030405" + ], + "primary peritoneal carcinoma": [ + "HP:0030406" + ], + "pineocytoma": [ + "HP:0030407" + ], + "pineoblastoma": [ + "HP:0030408" + ], + "pinealoblastoma": [ + "HP:0030408" + ], + "renal transitional cell carcinoma": [ + "HP:0030409" + ], + "renal tcc": [ + "HP:0030409" + ], + "renal urothelial carcinoma": [ + "HP:0030409" + ], + "transitional renal cell carcinoma": [ + "HP:0030409" + ], + "sebaceous gland carcinoma": [ + "HP:0030410" + ], + "sebaceous carcinoma": [ + "HP:0030410" + ], + "jejunal adenocarcinoma": [ + "HP:0030411" + ], + "ileal adenocarcinoma": [ + "HP:0030412" + ], + "squamous cell carcinoma of the tongue": [ + "HP:0030413" + ], + "verrucous cell carcinoma of the tongue": [ + "HP:0030414" + ], + "sarcomatoid carcinoma of the tongue": [ + "HP:0030415" + ], + "spindle cell carcinoma of the tongue": [ + "HP:0030415" + ], + "vulvar neoplasm": [ + "HP:0030416" + ], + "neoplasm of the vulva": [ + "HP:0030416" + ], + "tumor of the vulva": [ + "HP:0030416" + ], + "tumour of the vulva": [ + "HP:0030416" + ], + "squamous cell carcinoma of the vulva": [ + "HP:0030417" + ], + "vulval squamous cell carcinoma": [ + "HP:0030417" + ], + "vulvar melanoma": [ + "HP:0030418" + ], + "bartholin gland carcinoma": [ + "HP:0030419" + ], + "vulvar adenocarcinoma": [ + "HP:0030420" + ], + "epididymal neoplasm": [ + "HP:0030421" + ], + "obsolete papillary cystadenoma of the epididymis": [ + "HP:0030422" + ], + "splenic cyst": [ + "HP:0030423" + ], + "cyst on spleen": [ + "HP:0030423" + ], + "epididymal cyst": [ + "HP:0030424" + ], + "epididymal cysts": [ + "HP:0030424" + ], + "calcified ovarian cyst": [ + "HP:0030425" + ], + "ossify fibroma": [ + "HP:0030426" + ], + "ossifying fibroma": [ + "HP:0030426" + ], + "ossify fibroma of the jaw": [ + "HP:0030427" + ], + "ossifying fibroma of the jaw": [ + "HP:0030427" + ], + "cutaneous myxoma": [ + "HP:0030428" + ], + "juvenile nasopharyngeal angiofibroma": [ + "HP:0030429" + ], + "neuroma": [ + "HP:0030430" + ], + "nerve tumor": [ + "HP:0030430" + ], + "nerve tumour": [ + "HP:0030430" + ], + "pinch nerve": [ + "HP:0030430" + ], + "pinched nerve": [ + "HP:0030430" + ], + "osteochondroma": [ + "HP:0030431" + ], + "osteocartilaginous exostosis": [ + "HP:0030431" + ], + "osteocartilaginous exostoses": [ + "HP:0030431" + ], + "osteochondromas": [ + "HP:0030431" + ], + "chondroblastoma": [ + "HP:0030432" + ], + "osteoid osteoma": [ + "HP:0030433" + ], + "pilomatrixoma": [ + "HP:0030434" + ], + "fibrofolliculoma": [ + "HP:0030436" + ], + "fibrofolliculomas": [ + "HP:0030436" + ], + "anal canal neoplasm": [ + "HP:0030437" + ], + "anal canal tumor": [ + "HP:0030437" + ], + "anal canal tumour": [ + "HP:0030437" + ], + "anal canal squamous cell carcinoma": [ + "HP:0030438" + ], + "anal canal adenocarcinoma": [ + "HP:0030439" + ], + "anal margin neoplasm": [ + "HP:0030440" + ], + "anal margin paget 's disease": [ + "HP:0030441" + ], + "anal margin squamous cell carcinoma": [ + "HP:0030442" + ], + "anal margin basal cell carcinoma": [ + "HP:0030443" + ], + "anal margin melanoma": [ + "HP:0030444" + ], + "pulmonary carcinoid tumor": [ + "HP:0030445" + ], + "lung carcinoid tumor": [ + "HP:0030445" + ], + "lung carcinoid tumour": [ + "HP:0030445" + ], + "pulmonary carcinoid tumour": [ + "HP:0030445" + ], + "atypical pulmonary carcinoid tumor": [ + "HP:0030446" + ], + "atypical pulmonary carcinoid tumour": [ + "HP:0030446" + ], + "merkel cell skin cancer": [ + "HP:0030447" + ], + "anaplastic carcinoma of the skin": [ + "HP:0030447" + ], + "cutaneous apudoma": [ + "HP:0030447" + ], + "merkel cell cancer of the skin": [ + "HP:0030447" + ], + "neuroendocrine carcinoma of the skin": [ + "HP:0030447" + ], + "neuroendocrine tumor of the skin": [ + "HP:0030447" + ], + "neuroendocrine tumour of the skin": [ + "HP:0030447" + ], + "primary small cell carcinoma of the skin": [ + "HP:0030447" + ], + "primary undifferentiated carcinoma of the skin": [ + "HP:0030447" + ], + "soft tissue sarcoma": [ + "HP:0030448" + ], + "soft tissue sarcomas": [ + "HP:0030448" + ], + "therapeutic abortion": [ + "HP:0030449" + ], + "neuroplasm of the autonomic nervous system": [ + "HP:0030450" + ], + "mesenteric cyst": [ + "HP:0030451" + ], + "chylolymphatic mesenteric cyst": [ + "HP:0030452" + ], + "abnormal visual electrophysiology": [ + "HP:0030453" + ], + "abnormal electrooculogram": [ + "HP:0030454" + ], + "abnormal eog": [ + "HP:0030454" + ], + "abnormality of pattern visual evoke potential": [ + "HP:0030455" + ], + "abnormality of pattern visual evoked potentials": [ + "HP:0030455" + ], + "abnormality of pattern onset / offset visual evoked potential": [ + "HP:0030456" + ], + "abnormality of pattern onset / offset visual evoked potentials": [ + "HP:0030456" + ], + "abnormality of pattern onset / offset vep": [ + "HP:0030456" + ], + "abnormal amplitude of pattern onset / offset visual evoked potential": [ + "HP:0030457" + ], + "abnormal amplitude of pattern onset / offset visual evoked potentials": [ + "HP:0030457" + ], + "abnormal amplitude of pattern onset / offset vep": [ + "HP:0030457" + ], + "abnormal timing of pattern onset / offset visual evoked potential": [ + "HP:0030458" + ], + "abnormal timing of pattern onset / offset visual evoked potentials": [ + "HP:0030458" + ], + "abnormal timing of pattern reversal visual evoke potential": [ + "HP:0030460" + ], + "abnormal timing of pattern reversal visual evoked potentials": [ + "HP:0030460" + ], + "abnormal timing of flash visual evoke potential": [ + "HP:0030461" + ], + "abnormal timing of flash visual evoked potentials": [ + "HP:0030461" + ], + "abnormal amplitude of flash visual evoke potential": [ + "HP:0030462" + ], + "abnormal amplitude of flash visual evoked potentials": [ + "HP:0030462" + ], + "asymmetrical distribution of flash visual evoke potential": [ + "HP:0030463" + ], + "asymmetrical distribution of flash visual evoked potentials": [ + "HP:0030463" + ], + "crossed asymmetry of flash visual evoke potential": [ + "HP:0030463" + ], + "crossed asymmetry of flash visual evoked potentials": [ + "HP:0030463" + ], + "asymmetrical distribution of pattern reversal visual evoke potential": [ + "HP:0030464" + ], + "asymmetrical distribution of pattern reversal visual evoked potentials": [ + "HP:0030464" + ], + "crossed asymmetry of pattern reversal visual evoke potential": [ + "HP:0030464" + ], + "crossed asymmetry of pattern reversal visual evoked potentials": [ + "HP:0030464" + ], + "undetectable light - adapt electroretinogram": [ + "HP:0030465" + ], + "undetectable light - adapted electroretinogram": [ + "HP:0030465" + ], + "absent photopic ( cone ) responses on erg": [ + "HP:0030465" + ], + "non - detectable photopic erg": [ + "HP:0030465" + ], + "abnormal full - field electroretinogram": [ + "HP:0030466" + ], + "abnormal pattern electroretinogram": [ + "HP:0030467" + ], + "abnormal multifocal electroretinogram": [ + "HP:0030468" + ], + "abnormal dark - adapt electroretinogram": [ + "HP:0030469" + ], + "abnormal dark - adapted electroretinogram": [ + "HP:0030469" + ], + "abnormal dark - adapted bright flash electroretinogram": [ + "HP:0030470" + ], + "abnormal dark - adapt dim flash electroretinogram": [ + "HP:0030471" + ], + "abnormal dark - adapted dim flash electroretinogram": [ + "HP:0030471" + ], + "abnormal light - adapt single flash electroretinogram": [ + "HP:0030472" + ], + "abnormal light - adapted single flash electroretinogram": [ + "HP:0030472" + ], + "abnormal light - adapt flicker electroretinogram": [ + "HP:0030473" + ], + "abnormal light - adapted flicker electroretinogram": [ + "HP:0030473" + ], + "abnormal light - adapt 30hz flicker electroretinogram": [ + "HP:0030473" + ], + "abnormal light - adapted 30hz flicker electroretinogram": [ + "HP:0030473" + ], + "abnormal light - adapt 30hz flicker erg": [ + "HP:0030473" + ], + "abnormal light - adapted 30hz flicker erg": [ + "HP:0030473" + ], + "abnormal light - adapt flicker erg": [ + "HP:0030473" + ], + "abnormal light - adapted flicker erg": [ + "HP:0030473" + ], + "undetectable dark - adapt electroretinogram": [ + "HP:0030474" + ], + "undetectable dark - adapted electroretinogram": [ + "HP:0030474" + ], + "abnormal timing of dark - adapted dim flash electroretinogram": [ + "HP:0030475" + ], + "abnormal amplitude of dark - adapted dim flash electroretinogram": [ + "HP:0030476" + ], + "abnormal timing of dark - adapted bright flash electroretinogram": [ + "HP:0030477" + ], + "abnormal amplitude of dark - adapted bright flash electroretinogram": [ + "HP:0030478" + ], + "abnormal amplitude of light - adapt flicker electroretinogram": [ + "HP:0030479" + ], + "abnormal amplitude of light - adapted flicker electroretinogram": [ + "HP:0030479" + ], + "abnormal timing of light - adapt flicker electroretinogram": [ + "HP:0030480" + ], + "abnormal timing of light - adapted flicker electroretinogram": [ + "HP:0030480" + ], + "abnormal amplitude of light - adapt single flash electroretinogram": [ + "HP:0030481" + ], + "abnormal amplitude of light - adapted single flash electroretinogram": [ + "HP:0030481" + ], + "abnormal timing of light - adapt single flash electroretinogram": [ 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microaneurysm / hemorrhage": [ + "HP:0030494" + ], + "abnormality morphology of the macular vasculature": [ + "HP:0030495" + ], + "abnormality of macular vasculature": [ + "HP:0030495" + ], + "macular exudate": [ + "HP:0030496" + ], + "macular exudates": [ + "HP:0030496" + ], + "macular exudation": [ + "HP:0030496" + ], + "macular cotton wool spot": [ + "HP:0030497" + ], + "macular thickening": [ + "HP:0030498" + ], + "macular drusen": [ + "HP:0030499" + ], + "lipid accumulation in macula": [ + "HP:0030499" + ], + "yellow / white lesion of the macula": [ + "HP:0030500" + ], + "yellow / white lesions of the macula": [ + "HP:0030500" + ], + "macular crystal": [ + "HP:0030501" + ], + "macular crystals": [ + "HP:0030501" + ], + "retinoschisis": [ + "HP:0030502" + ], + "macular telangiectasia": [ + "HP:0030503" + ], + "juxtafoveal telangiectasia": [ + "HP:0030503" + ], + "parafoveal telangiectasia": [ + "HP:0030503" + ], + "group congenital hypertrophy of retinal pigment epithelium": [ + "HP:0030504" + ], + "grouped congenital hypertrophy of retinal pigment epithelium": [ + "HP:0030504" + ], + "bear track congenital hypertrophy of retinal pigment epithelium": [ + "HP:0030504" + ], + "nummular pigmentation of the fundus": [ + "HP:0030505" + ], + "nummular pigmentation of the retina": [ + "HP:0030505" + ], + "yellow / white lesion of the retina": [ + "HP:0030506" + ], + "yellow / white lesions of the retina": [ + "HP:0030506" + ], + "retinal crystal": [ + "HP:0030507" + ], + "retinal crystals": [ + "HP:0030507" + ], + "retinal cavernous hemangioma": [ + "HP:0030508" + ], + "retinal cavernous haemangioma": [ + "HP:0030508" + ], + "retinal racemose hemangioma": [ + "HP:0030509" + ], + "retinal racemose haemangioma": [ + "HP:0030509" + ], + "combine hamartoma of the retinal pigment epithelium and retina": [ + "HP:0030510" + ], + "combined hamartoma of the retinal pigment epithelium and retina": [ + "HP:0030510" + ], + "bradyopsia": [ + "HP:0030511" + ], + "difficulty see move object": [ + "HP:0030511" + ], + "difficulty seeing moving objects": [ + "HP:0030511" + ], + "difficulty adjust to change in luminance": [ + "HP:0030512" + ], + "difficulty adjusting to changes in luminance": [ + "HP:0030512" + ], + "difficulty adjust from light to dark": [ + "HP:0030513" + ], + "difficulty adjusting from light to dark": [ + "HP:0030513" + ], + "difficulty adjust from dark to light": [ + "HP:0030514" + ], + "difficulty adjusting from dark to light": [ + "HP:0030514" + ], + "moderately reduce visual acuity": [ + "HP:0030515" + ], + "moderately reduced visual acuity": [ + "HP:0030515" + ], + "moderate reduction in visual acuity": [ + "HP:0030515" + ], + "moderate vision loss": [ + "HP:0030515" + ], + "moderate visual impairment": [ + "HP:0030515" + ], + "moderate visual loss": [ + "HP:0030515" + ], + "homonymous hemianopia": [ + "HP:0030516" + ], + "homonymous hemianopsia": [ + "HP:0030516" + ], + "heteronymous hemianopia": [ + "HP:0030517" + ], + "heteronymous hemianopsia": [ + "HP:0030517" + ], + "congruous homonymous hemianopia": [ + "HP:0030518" + ], + "congruous hemianopsia": [ + "HP:0030518" + ], + "congruous heteronymous hemianopia": [ + "HP:0030519" + ], + "binasal hemianopia": [ + "HP:0030520" + ], + "bitemporal hemianopia": [ + "HP:0030521" + ], + "mild constriction of peripheral visual field": [ + "HP:0030522" + ], + "mild peripheral visual field loss": [ + "HP:0030522" + ], + "obsolete peripheral visual field constriction with 40 - 50 degree central field preserve": [ + "HP:0030523" + ], + "obsolete peripheral visual field constriction with 40 - 50 degrees central field preserved": [ + "HP:0030523" + ], + "obsolete peripheral visual field constriction with 30 - 39 degree central field preserve": [ + "HP:0030524" + ], + "obsolete peripheral visual field constriction with 30 - 39 degrees central field preserved": [ + "HP:0030524" + ], + "moderate constriction of peripheral visual field": [ + "HP:0030525" + ], + "moderate peripheral visual field loss": [ + "HP:0030525" + ], + "severe constriction of peripheral visual field": [ + "HP:0030526" + ], + "severe peripheral visual field loss": [ + "HP:0030526" + ], + "very severe constriction of peripheral visual field": [ + "HP:0030527" + ], + "very severe peripheral visual field loss": [ + "HP:0030527" + ], + "paracentral scotoma": [ + "HP:0030528" + ], + "ring scotoma": [ + "HP:0030529" + ], + "arcuate scotoma": [ + "HP:0030530" + ], + "arc - shape blind spot": [ + "HP:0030530" + ], + "arc - shaped blind spot": [ + "HP:0030530" + ], + "altitudinal visual field defect": [ + "HP:0030531" + ], + "visual acuity test abnormality": [ + "HP:0030532" + ], + "abnormal unaided visual acuity test": [ + "HP:0030533" + ], + "abnormal best correct visual acuity test": [ + "HP:0030534" + ], + "abnormal best corrected visual acuity test": [ + "HP:0030534" + ], + "abnormal pinhole visual acuity test": [ + "HP:0030535" + ], + "unaided visual acuity 0.1 logmar": [ + "HP:0030536" + ], + "unaided visual acuity 0.2 logmar": [ + "HP:0030537" + ], + "unaided visual acuity 0.3 logmar": [ + "HP:0030538" + ], + "unaided visual acuity 0.4 logmar": [ + "HP:0030539" + ], + "unaided visual acuity 0.5 logmar": [ + "HP:0030540" + ], + "unaided visual acuity 0.6 logmar": [ + "HP:0030541" + ], + "unaided visual acuity 0.7 logmar": [ + "HP:0030542" + ], + "unaided visual acuity 0.8 logmar": [ + "HP:0030543" + ], + "unaided visual acuity 0.9 logmar": [ + "HP:0030544" + ], + "unaided visual acuity 1.0 logmar": [ + "HP:0030545" + ], + "unaided visual acuity 1.1 logmar": [ + "HP:0030546" + ], + "unaided visual acuity 1.2 logmar": [ + "HP:0030547" + ], + "unaided visual acuity 1.3 logmar": [ + "HP:0030548" + ], + "unaided visual acuity 2.0 logmar": [ + "HP:0030549" + ], + "unaided visual acuity 3.0 logmar": [ + "HP:0030550" + ], + "visual acuity light perception with projection": [ + "HP:0030551" + ], + "visual acuity light perception without projection": [ + "HP:0030552" + ], + "visual acuity no light perception": [ + "HP:0030553" + ], + "best correct visual acuity 0.1 logmar": [ + "HP:0030554" + ], + "best corrected visual acuity 0.1 logmar": [ + "HP:0030554" + ], + "best correct visual acuity 0.2 logmar": [ + "HP:0030555" + ], + "best corrected visual acuity 0.2 logmar": [ + "HP:0030555" + ], + "best correct visual acuity 0.3 logmar": [ + "HP:0030556" + ], + "best corrected visual acuity 0.3 logmar": [ + "HP:0030556" + ], + "best correct visual acuity 0.4 logmar": [ + "HP:0030557" + ], + "best corrected visual acuity 0.4 logmar": [ + "HP:0030557" + ], + "best correct visual acuity 0.5 logmar": [ + "HP:0030558" + ], + "best corrected visual acuity 0.5 logmar": [ + "HP:0030558" + ], + "best correct visual acuity 0.7 logmar": [ + "HP:0030559" + ], + "best corrected visual acuity 0.7 logmar": [ + "HP:0030559" + ], + "best correct visual acuity 0.6 logmar": [ + "HP:0030560" + ], + "best corrected visual acuity 0.6 logmar": [ + "HP:0030560" + ], + "best correct visual acuity 0.8 logmar": [ + "HP:0030561" + ], + "best corrected visual acuity 0.8 logmar": [ + "HP:0030561" + ], + "best correct visual acuity 0.9 logmar": [ + "HP:0030562" + ], + "best corrected visual acuity 0.9 logmar": [ + "HP:0030562" + ], + "best correct visual acuity 1.0 logmar": [ + "HP:0030563" + ], + "best corrected visual acuity 1.0 logmar": [ + "HP:0030563" + ], + "best correct visual acuity 1.1 logmar": [ + "HP:0030564" + ], + "best corrected visual acuity 1.1 logmar": [ + "HP:0030564" + ], + "best correct visual acuity 1.2 logmar": [ + "HP:0030565" + ], + "best corrected visual acuity 1.2 logmar": [ + "HP:0030565" + ], + "best correct visual acuity 1.3 logmar": [ + "HP:0030566" + ], + "best corrected visual acuity 1.3 logmar": [ + "HP:0030566" + ], + "best correct visual acuity 2.0 logmar": [ + "HP:0030567" + ], + "best corrected visual acuity 2.0 logmar": [ + "HP:0030567" + ], + "best correct visual acuity 3.0 logmar": [ + "HP:0030568" + ], + "best corrected visual acuity 3.0 logmar": [ + "HP:0030568" + ], + "pinhole visual acuity 0.1 logmar": [ + "HP:0030569" + ], + "pinhole visual acuity 0.2 logmar": [ + "HP:0030570" + ], + "pinhole visual acuity 0.3 logmar": [ + "HP:0030571" + ], + "pinhole visual acuity 0.4 logmar": [ + "HP:0030572" + ], + "pinhole visual acuity 0.5 logmar": [ + "HP:0030573" + ], + "pinhole visual acuity 0.6 logmar": [ + "HP:0030574" + ], + "pinhole visual acuity 0.7 logmar": [ + "HP:0030575" + ], + "pinhole visual acuity 0.8 logmar": [ + "HP:0030576" + ], + "pinhole visual acuity 0.9 logmar": [ + "HP:0030577" + ], + "pinhole visual acuity 1.0 logmar": [ + "HP:0030578" + ], + "pinhole visual acuity 1.1 logmar": [ + "HP:0030579" + ], + "pinhole visual acuity 1.2 logmar": [ + "HP:0030580" + ], + "pinhole visual acuity 1.3 logmar": [ + "HP:0030581" + ], + "pinhole visual acuity 2.0 logmar": [ + "HP:0030582" + ], + "pinhole visual acuity 3.0 logmar": [ + "HP:0030583" + ], + "color vision test abnormality": [ + "HP:0030584" + ], + "colour vision test abnormality": [ + "HP:0030584" + ], + "red desaturation": [ + "HP:0030585" + ], + "abnormal ishihara plate test": [ + "HP:0030586" + ], + "abnormal hardy - rand - rittler plate test": [ + "HP:0030587" + ], + "abnormal visual field test": [ + "HP:0030588" + ], + "abnormal confrontational visual field test": [ + "HP:0030589" + ], + "abnormal amsler grid test": [ + "HP:0030590" + ], + "abnormal kinetic perimetry test": [ + "HP:0030591" + ], + "abnormal static perimetry test": [ + "HP:0030592" + ], + "abnormal manual kinetic perimetry test": [ + "HP:0030593" + ], + "abnormal automate kinetic perimetry test": [ + "HP:0030594" + ], + "abnormal automated kinetic perimetry test": [ + "HP:0030594" + ], + "abnormal static automate perimetry test": [ + "HP:0030595" + ], + "abnormal static automated perimetry test": [ + "HP:0030595" + ], + "abnormal humphrey sita 30 - 2 perimetry test": [ + "HP:0030596" + ], + "abnormal humphrey sita 24 - 2 perimetry test": [ + "HP:0030597" + ], + "abnormal humphrey sita 10 - 2 perimetry test": [ + "HP:0030598" + ], + "abnormal estermann grid perimetry test": [ + "HP:0030599" + ], + "abnormal posterior segment imaging": [ + "HP:0030601" + ], + "abnormal fundus autofluorescence imaging": [ + "HP:0030602" + ], + "abnormal optical coherence tomography": [ + "HP:0030603" + ], + "abnormal fundus fluorescein angiography": [ + "HP:0030604" + ], + "abnormal indocyanine green angiography": [ + "HP:0030605" + ], + "abnormal oct - measure macular thickness": [ + "HP:0030606" + ], + "abnormal oct - measured macular thickness": [ + "HP:0030606" + ], + "reduce oct - measure macular thickness": [ + "HP:0030607" + ], + "reduced oct - measured macular thickness": [ + "HP:0030607" + ], + "increase oct - measure macular thickness": [ + "HP:0030608" + ], + "increased oct - measured macular thickness": [ + "HP:0030608" + ], + "photoreceptor layer loss on macular oct": [ + "HP:0030609" + ], + "photoreceptor outer segment loss on macular oct": [ + "HP:0030610" + ], + "retinal pigment epithelial loss on macular oct": [ + "HP:0030611" + ], + "abnormal retinal morphology on macular oct": [ + "HP:0030612" + ], + "abnormal foveal morphology on macular oct": [ + "HP:0030613" + ], + "foveal photoreceptor layer loss on macular oct": [ + "HP:0030614" + ], + "foveal photoreceptor outer segment loss on macular oct": [ + "HP:0030615" + ], + "foveal retinal pigment epithelial loss on macular oct": [ + "HP:0030616" + ], + "abnormal oct - measure foveal thickness": [ + "HP:0030617" + ], + "abnormal oct - measured foveal thickness": [ + "HP:0030617" + ], + "increase oct - measure foveal thickness": [ + "HP:0030618" + ], + "increased oct - measured foveal thickness": [ + "HP:0030618" + ], + "reduce oct - measure foveal thickness": [ + "HP:0030619" + ], + "reduced oct - measured foveal thickness": [ + "HP:0030619" + ], + "inner retinal layer loss on macular oct": [ + "HP:0030620" + ], + "foveal inner retinal layer loss on macular oct": [ + "HP:0030621" + ], + "abnormal foveal pit on macular oct": [ + "HP:0030622" + ], + "intraretinal hyporeflective space on macular oct": [ + "HP:0030623" + ], + "intraretinal hyporeflective spaces on macular oct": [ + "HP:0030623" + ], + "subretinal hyporeflective space on macular oct": [ + "HP:0030624" + ], + "subretinal hyporeflective spaces on macular oct": [ + "HP:0030624" + ], + "hyporeflective space on macular oct": [ + "HP:0030625" + ], + "hyporeflective spaces on macular oct": [ + "HP:0030625" + ], + "foveal intraretinal hyporeflective space on macular oct": [ + "HP:0030626" + ], + "foveal intraretinal hyporeflective spaces on macular oct": [ + "HP:0030626" + ], + "foveal hyporeflective space on macular oct": [ + "HP:0030627" + ], + "foveal hyporeflective spaces on macular oct": [ + "HP:0030627" + ], + "foveal subretinal hyporeflective space on macular oct": [ + "HP:0030628" + ], + "foveal subretinal hyporeflective spaces on macular oct": [ + "HP:0030628" + ], + "perifoveal ring of hyperautofluorescence": [ + "HP:0030629" + ], + "irregular central macular autofluorescence": [ + "HP:0030630" + ], + "hyperautofluorescent macular lesion": [ + "HP:0030631" + ], + "hypoautofluorescent macular lesion": [ + "HP:0030632" + ], + "hypo - autofluorescent macular lesion": [ + "HP:0030632" + ], + "perifoveal ring of hyperautofluorescence surround by normal autofluorescence": [ + "HP:0030633" + ], + "perifoveal ring of hyperautofluorescence surrounded by normal autofluorescence": [ + "HP:0030633" + ], + "perifoveal ring of hyperautofluorescence surround by abnormal autofluorescence": [ + "HP:0030634" + ], + "perifoveal ring of hyperautofluorescence surrounded by abnormal autofluorescence": [ + "HP:0030634" + ], + "retinal dystrophy with early macular involvement": [ + "HP:0030635" + ], + "occult macular dystrophy": [ + "HP:0030636" + ], + "congenital stationary cone dysfunction": [ + "HP:0030637" + ], + "cone dysfunction": [ + "HP:0030637" + ], + "cone dysfunction syndrome": [ + "HP:0030637" + ], + "congenital stationary night blindness with normal fundus": [ + "HP:0030638" + ], + "congenital stationary night blindness with abnormal fundus": [ + "HP:0030639" + ], + "complete congenital stationary night blindness": [ + "HP:0030640" + ], + "incomplete congenital stationary night blindness": [ + "HP:0030641" + ], + "fundus albipunctatus": [ + "HP:0030642" + ], + "vitelliform - like retinal lesion": [ + "HP:0030643" + ], + "vitelliform - like retinal lesions": [ + "HP:0030643" + ], + "blind - spot enlargment": [ + "HP:0030644" + ], + "blind spot enlargment": [ + "HP:0030644" + ], + "central": [ + "HP:0030645" + ], + "peripheral": [ + "HP:0030646" + ], + "paracentral": [ + "HP:0030647" + ], + "midperipheral": [ + "HP:0030648" + ], + "mid - peripheral": [ + "HP:0030648" + ], + "pericentral": [ + "HP:0030649" + ], + "focal": [ + "HP:0030650" + ], + "multifocal": [ + "HP:0030651" + ], + "vitreous haze": [ + "HP:0030652" + ], + "umbilical cord cyst": [ + "HP:0030654" + ], + "umbilical cord knot": [ + "HP:0030655" + ], + "umbilical vein varix": [ + "HP:0030656" + ], + "umbilical cord hematoma": [ + "HP:0030657" + ], + "umbilical cord haematoma": [ + "HP:0030657" + ], + "marginal umbilical cord insertion": [ + "HP:0030658" + ], + "marginal cord insertion": [ + "HP:0030658" + ], + "velamentous cord insertion": [ + "HP:0030659" + ], + "furcate cord insertion": [ + "HP:0030660" + ], + "vitreous snowball": [ + "HP:0030661" + ], + "vitreous snowballs": [ + "HP:0030661" + ], + "vitreous inflammatory cell": [ + "HP:0030662" + ], + "vitreous inflammatory cells": [ + "HP:0030662" + ], + "optically empty vitreous": [ + "HP:0030663" + ], + "beevor 's sign": [ + "HP:0030664" + ], + "rubral tremor": [ + "HP:0030665" + ], + "holmes ' tremor": [ + "HP:0030665" + ], + "retinal neovascularization": [ + "HP:0030666" + ], + "retinal neovascularisation": [ + "HP:0030666" + ], + "peripheral retinal neovascularization": [ + "HP:0030667" + ], + "periorbital dermoid cyst": [ + "HP:0030668" + ], + "abnormal ocular adnexa morphology": [ + "HP:0030669" + ], + "hamartoma of the orbital region": [ + "HP:0030670" + ], + "abnormal common tendinous ring morphology": [ + "HP:0030671" + ], + "abnormality of the common tendinous ring": [ + "HP:0030671" + ], + "asteroid hyalosis": [ + "HP:0030672" + ], + "erosive vitreoretinopathy": [ + "HP:0030673" + ], + "antenatal onset": [ + "HP:0030674" + ], + "contracture of proximal interphalangeal joint of 2nd - 5th finger": [ + "HP:0030675" + ], + "contracture of proximal interphalangeal joints of 2nd - 5th fingers": [ + "HP:0030675" + ], + "satyr ear": [ + "HP:0030676" + ], + "devil ear": [ + "HP:0030676" + ], + "mozart ear": [ + "HP:0030677" + ], + "ash - leaf spot": [ + "HP:0030679" + ], + "abnormality of cardiovascular system morphology": [ + "HP:0030680" + ], + "cardiovascular malformation": [ + "HP:0030680" + ], + "cardiovascular malformations": [ + "HP:0030680" + ], + "abnormal morphology of myocardial trabecula": [ + "HP:0030681" + ], + "abnormal morphology of myocardial trabeculae": [ + "HP:0030681" + ], + "leave ventricular noncompaction": [ + "HP:0030682" + ], + "left ventricular noncompaction": [ + "HP:0030682" + ], + "vaginitis": [ + "HP:0030683" + ], + "vulvovaginitis": [ + "HP:0030683" + ], + "abnormal adiponectin level": [ + "HP:0030684" + ], + "decrease adiponectin level": [ + "HP:0030685" + ], + "decreased adiponectin level": [ + "HP:0030685" + ], + "increase adiponectin level": [ + "HP:0030686" + ], + "increased adiponectin level": [ + "HP:0030686" + ], + "abnormal glucagon level": [ + "HP:0030687" + ], + "increase glucagon level": [ + "HP:0030688" + ], + "increased glucagon level": [ + "HP:0030688" + ], + "decrease glucagon level": [ + "HP:0030689" + ], + "decreased glucagon level": [ + "HP:0030689" + ], + "gingival cleft": [ + "HP:0030690" + ], + "divergence nystagmus": [ + "HP:0030691" + ], + "brain neoplasm": [ + "HP:0030692" + ], + "brain tumor": [ + "HP:0030692" + ], + "brain tumour": [ + "HP:0030692" + ], + "supratentorial neoplasm": [ + "HP:0030693" + ], + "pineal parenchymal tumor": [ + "HP:0030693" + ], + "pineal parenchymal tumour": [ + "HP:0030693" + ], + "pineal parenchymal cell neoplasm": [ + "HP:0030694" + ], + "ranula": [ + "HP:0030706" + ], + "sublingual cyst": [ + "HP:0030706" + ], + "sublingual ptyalocele": [ + "HP:0030706" + ], + "unilateral lung agenesis": [ + "HP:0030707" + ], + "unilateral pulmonary agenesis": [ + "HP:0030707" + ], + "myeloschisis": [ + "HP:0030708" + ], + "myelocystocele": [ + "HP:0030709" + ], + "lipomeningocele": [ + "HP:0030710" + ], + "hydrocolpos": [ + "HP:0030711" + ], + "uterine synechiae": [ + "HP:0030712" + ], + "asherman syndrome": [ + "HP:0030712" + ], + "vein of galen aneurysmal malformation": [ + "HP:0030713" + ], + "median prosencephalic arteriovenous fistula": [ + "HP:0030713" + ], + "vein of galen aneurysm": [ + "HP:0030713" + ], + "vein of galen malformation": [ + "HP:0030713" + ], + 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foetal demise of one twin after midgestation": [ + "HP:0030753" + ], + "single - twin demise": [ + "HP:0030753" + ], + "allantoic cyst": [ + "HP:0030754" + ], + "craniofacial teratoma": [ + "HP:0030755" + ], + "erythrodontia": [ + "HP:0030756" + ], + "red teeth": [ + "HP:0030756" + ], + "tooth abscess": [ + "HP:0030757" + ], + "dental abscess": [ + "HP:0030757" + ], + "dentoalveolar abscess": [ + "HP:0030757" + ], + "periapical tooth abscess": [ + "HP:0030758" + ], + "adipocyte hypertrophy": [ + "HP:0030759" + ], + "fat cell hypertrophy": [ + "HP:0030759" + ], + "renal fibrosis": [ + "HP:0030760" + ], + "kidney fibrosis": [ + "HP:0030760" + ], + "obsolete renal glomerular fibrosis": [ + "HP:0030761" + ], + "mesangiolysis": [ + "HP:0030762" + ], + "amniotic sheet": [ + "HP:0030763" + ], + "amniotic shelf": [ + "HP:0030763" + ], + "ochronosis": [ + "HP:0030764" + ], + "sleep terror": [ + "HP:0030765" + ], + "night terror": [ + "HP:0030765" + ], + "pavor nocturnus": [ + "HP:0030765" + ], 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neoplasm": [ + "HP:0030792" + ], + "jaw swell": [ + "HP:0030793" + ], + "jaw swelling": [ + "HP:0030793" + ], + "abnormal c - peptide level": [ + "HP:0030794" + ], + "abnormal c peptide level": [ + "HP:0030794" + ], + "reduce c - peptide level": [ + "HP:0030795" + ], + "reduced c - peptide level": [ + "HP:0030795" + ], + "reduce c peptide level": [ + "HP:0030795" + ], + "reduced c peptide level": [ + "HP:0030795" + ], + "increase c - peptide level": [ + "HP:0030796" + ], + "increased c - peptide level": [ + "HP:0030796" + ], + "increase c peptide level": [ + "HP:0030796" + ], + "increased c peptide level": [ + "HP:0030796" + ], + "reduced volume of central subdivision of bed nucleus of stria terminalis": [ + "HP:0030797" + ], + "abnormality of the bed nucleus of stria terminalis": [ + "HP:0030798" + ], + "scaphocephaly": [ + "HP:0030799" + ], + "abnormal visual accommodation": [ + "HP:0030800" + ], + "reduce visual accommodation": [ + "HP:0030801" + ], + "reduced visual accommodation": 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"tongue lipoma": [ + "HP:0030815" + ], + "gingival recession": [ + "HP:0030816" + ], + "gum recession": [ + "HP:0030816" + ], + "recede gum": [ + "HP:0030816" + ], + "receding gums": [ + "HP:0030816" + ], + "beak nail": [ + "HP:0030817" + ], + "beaked nails": [ + "HP:0030817" + ], + "central nail canal": [ + "HP:0030818" + ], + "median nail dystrophy": [ + "HP:0030818" + ], + "ski jump nail": [ + "HP:0030819" + ], + "upslanting nail": [ + "HP:0030819" + ], + "upward angulation of nail": [ + "HP:0030819" + ], + "hood eyelid": [ + "HP:0030820" + ], + "hooded eyelid": [ + "HP:0030820" + ], + "hood low eyelid": [ + "HP:0030821" + ], + "hooded lower eyelid": [ + "HP:0030821" + ], + "hood upper eyelid": [ + "HP:0030822" + ], + "hooded upper eyelid": [ + "HP:0030822" + ], + "scleral thickening": [ + "HP:0030823" + ], + "thick sclera": [ + "HP:0030823" + ], + "mizuo phenomenon": [ + "HP:0030824" + ], + "mizuo - nakamura phenomenon": [ + "HP:0030824" + ], + "absent foveal reflex": [ + 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jugular venous pressure": [ + "HP:0030848" + ], + "elevated jugular venous pressure": [ + "HP:0030848" + ], + "hepatojugular reflux": [ + "HP:0030849" + ], + "abnormal pulse pressure": [ + "HP:0030850" + ], + "low pulse pressure": [ + "HP:0030851" + ], + "high pulse pressure": [ + "HP:0030852" + ], + "heterotaxy": [ + "HP:0030853" + ], + "heterotaxia": [ + "HP:0030853" + ], + "scleral staphyloma": [ + "HP:0030854" + ], + "staphyloma": [ + "HP:0030854" + ], + "anterior staphyloma": [ + "HP:0030855" + ], + "posterior staphyloma": [ + "HP:0030856" + ], + "eye movement - induced pain": [ + "HP:0030857" + ], + "addictive behavior": [ + "HP:0030858" + ], + "addictive behaviour": [ + "HP:0030858" + ], + "anti - topoisomerase i antibody positivity": [ + "HP:0030859" + ], + "top1 antibody positivity": [ + "HP:0030859" + ], + "topoisomerase ( dna ) i antibody positivity": [ + "HP:0030859" + ], + "abnormal csf amyloid level": [ + "HP:0030860" + ], + "abnormal csf a [ beta ] 42 level": [ + 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growth - hormone response to insulin stimulation test": [ + "HP:0031079" + ], + "abnormal response to glucagon stimulation test": [ + "HP:0031080" + ], + "impaired cortisol response to glucagon stimulation test": [ + "HP:0031081" + ], + "impaired growth - hormone response to glucagon stimulation test": [ + "HP:0031082" + ], + "abnormal response to human chorionic gonadotrophin stimulation test": [ + "HP:0031083" + ], + "abnormal response to hcg stimulation test": [ + "HP:0031083" + ], + "excessive insulin response to glucagon test": [ + "HP:0031084" + ], + "decrease prealbumin level": [ + "HP:0031085" + ], + "decreased prealbumin level": [ + "HP:0031085" + ], + "ectopic ovary": [ + "HP:0031086" + ], + "undescended ovary": [ + "HP:0031086" + ], + "absent pubertal growth spurt": [ + "HP:0031087" + ], + "absent adolescent growth spurt": [ + "HP:0031087" + ], + "vaginal dryness": [ + "HP:0031088" + ], + "palatal edema": [ + "HP:0031089" + ], + "palatal oedema": [ + "HP:0031089" + ], + "palate edema": [ + "HP:0031089" + ], + "palate oedema": [ + "HP:0031089" + ], + "finger dactylitis": [ + "HP:0031090" + ], + "sausage finger": [ + "HP:0031090" + ], + "sausage fingers": [ + "HP:0031090" + ], + "toe dactylitis": [ + "HP:0031091" + ], + "sausage toe": [ + "HP:0031091" + ], + "sausage toes": [ + "HP:0031091" + ], + "spindle - shape finger": [ + "HP:0031092" + ], + "spindle - shaped finger": [ + "HP:0031092" + ], + "abnormal breast morphology": [ + "HP:0031093" + ], + "abnormal breast physiology": [ + "HP:0031094" + ], + "abnormal humerus morphology": [ + "HP:0031095" + ], + "delay vertebral ossification": [ + "HP:0031096" + ], + "delayed vertebral ossification": [ + "HP:0031096" + ], + "abnormal thyroid - stimulate hormone level": [ + "HP:0031097" + ], + "abnormal thyroid - stimulating hormone level": [ + "HP:0031097" + ], + "abnormal circulate thyrotropin concentration": [ + "HP:0031097" + ], + "abnormal circulating thyrotropin concentration": [ + "HP:0031097" + ], + "abnormal thyrotropin level": [ + "HP:0031097" + ], + "abnormal tsh level": [ + "HP:0031097" + ], + "decrease thyroid - stimulate hormone level": [ + "HP:0031098" + ], + "decreased thyroid - stimulating hormone level": [ + "HP:0031098" + ], + "decrease plasma tsh": [ + "HP:0031098" + ], + "decreased plasma tsh": [ + "HP:0031098" + ], + "decrease thyrotropin level": [ + "HP:0031098" + ], + "decreased thyrotropin level": [ + "HP:0031098" + ], + "abnormal circulate inhibin level": [ + "HP:0031099" + ], + "abnormal circulating inhibin level": [ + "HP:0031099" + ], + "decrease inhibin b level": [ + "HP:0031100" + ], + "decreased inhibin b level": [ + "HP:0031100" + ], + "abnormal circulate antimullerian hormone concentration": [ + "HP:0031101" + ], + "abnormal circulating antimullerian hormone concentration": [ + "HP:0031101" + ], + "abnormal antimullerian hormone level": [ + "HP:0031101" + ], + "increase antimullerian hormone level": [ + "HP:0031102" + ], + "increased antimullerian hormone level": [ + "HP:0031102" + ], + "increase plasma amh": [ + "HP:0031102" + ], + "increased plasma amh": [ + "HP:0031102" + ], + "decrease antimullerian hormone level": [ + "HP:0031103" + ], + "decreased antimullerian hormone level": [ + "HP:0031103" + ], + "decrease plasma amh": [ + "HP:0031103" + ], + "decreased plasma amh": [ + "HP:0031103" + ], + "insulin receptor antibody positivity": [ + "HP:0031104" + ], + "abnormal uterus morphology": [ + "HP:0031105" + ], + "t - shape uterus": [ + "HP:0031106" + ], + "t - shaped uterus": [ + "HP:0031106" + ], + "decrease fibular diameter": [ + "HP:0031107" + ], + "decreased fibular diameter": [ + "HP:0031107" + ], + "thin fibula": [ + "HP:0031107" + ], + "triceps weakness": [ + "HP:0031108" + ], + "agalactia": [ + "HP:0031109" + ], + "lactation incapacity": [ + "HP:0031109" + ], + "twin - to - twin transfusion": [ + "HP:0031110" + ], + "twin to twin transfusion syndrome": [ + "HP:0031110" + ], + "cutaneous hamartoma": [ + "HP:0031111" + ], + "skin hamartoma": [ + "HP:0031111" + ], + "purely bicuspid aortic valve": [ + "HP:0031117" + ], + "single raphe bicuspid aortic valve": [ + "HP:0031118" + ], + "bicuspid aortic valve with right - leave cusp fusion": [ + "HP:0031119" + ], + "bicuspid aortic valve with right - left cusp fusion": [ + "HP:0031119" + ], + "bicuspid aortic valve with right - noncoronary cusp fusion": [ + "HP:0031120" + ], + "bicuspid aortic valve with left - noncoronary cusp fusion": [ + "HP:0031121" + ], + "two - raphe bicuspid aortic valve": [ + "HP:0031122" + ], + "recurrent gastroenteritis": [ + "HP:0031123" + ], + "decrease platelet thromboxane a2 receptor": [ + "HP:0031124" + ], + "decreased platelet thromboxane a2 receptor": [ + "HP:0031124" + ], + "decrease platelet alpha - 2a - adrenergic receptor": [ + "HP:0031125" + ], + "decreased platelet alpha - 2a - adrenergic receptor": [ + "HP:0031125" + ], + "impaired clot retraction": [ + "HP:0031126" + ], + "impaired convulxin - induced platelet aggregation": [ + "HP:0031127" + ], + "impaired collagen - relate peptide - induced platelet aggregation": [ + "HP:0031128" + ], + "impaired collagen - related peptide - induced platelet aggregation": [ + "HP:0031128" + ], + "impaired phorbol myristate acetate - induced platelet aggregation": [ + "HP:0031129" + ], + "impaired calcium ionophore - induced platelet aggregation": [ + "HP:0031130" + ], + "impaired ca ionophore - induced platelet aggregation": [ + "HP:0031130" + ], + "impaired ca2+ ionophore - induced platelet aggregation": [ + "HP:0031130" + ], + "abnormal platelet phosphatidylserine exposure": [ + "HP:0031131" + ], + "impaired annexin v bind to platelet phosphatidylserine": [ + "HP:0031132" + ], + "impaired annexin v binding to platelet phosphatidylserine": [ + "HP:0031132" + ], + "increase annexin v bind to platelet phosphatidylserine": [ + "HP:0031133" + ], + "increased annexin v binding to platelet phosphatidylserine": [ + "HP:0031133" + ], + "cor triatrium sinister": [ 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echotexture": [ + "HP:0031144" + ], + "coarsened hepatic echotexture": [ + "HP:0031144" + ], + "starry sky appearance on hepatic sonography": [ + "HP:0031145" + ], + "impaired oral bolus formation": [ + "HP:0031146" + ], + "vitreomacular adhesion": [ + "HP:0031150" + ], + "vitreomacular traction": [ + "HP:0031151" + ], + "full - thickness macular hole": [ + "HP:0031152" + ], + "membranous vitreous appearance": [ + "HP:0031153" + ], + "membranous anomaly": [ + "HP:0031153" + ], + "membranous vitreous": [ + "HP:0031153" + ], + "membranous vitreous phenotype": [ + "HP:0031153" + ], + "bead vitreous appearance": [ + "HP:0031154" + ], + "beaded vitreous appearance": [ + "HP:0031154" + ], + "increase arden ratio of electrooculogram": [ + "HP:0031155" + ], + "increased arden ratio of electrooculogram": [ + "HP:0031155" + ], + "increase arden ratio of eog": [ + "HP:0031155" + ], + "increased arden ratio of eog": [ + "HP:0031155" + ], + "decrease platelet glycoprotein ib": [ + "HP:0031156" + ], 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[ + "HP:0031165" + ], + "multifocal onset seizure": [ + "HP:0031165" + ], + "multifocal onset seizures": [ + "HP:0031165" + ], + "eyelid myokymia": [ + "HP:0031166" + ], + "myokymia orbicularis": [ + "HP:0031166" + ], + "orbicularis myokymia": [ + "HP:0031166" + ], + "trigger by ingestion of potassium - rich food": [ + "HP:0031167" + ], + "triggered by ingestion of potassium - rich food": [ + "HP:0031167" + ], + "potassium - rich food trigger symptom": [ + "HP:0031167" + ], + "potassium - rich food triggered symptoms": [ + "HP:0031167" + ], + "trigger by ingestion of k - rich food": [ + "HP:0031167" + ], + "triggered by ingestion of k - rich food": [ + "HP:0031167" + ], + "postterm pregnancy": [ + "HP:0031169" + ], + "female fetal virilization": [ + "HP:0031170" + ], + "female foetal virilization": [ + "HP:0031170" + ], + "femoral spur": [ + "HP:0031171" + ], + "spurring of femur": [ + "HP:0031171" + ], + "sectoral retinitis pigmentosa": [ + "HP:0031172" + ], + "tibial spur": [ + 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level": [ + "HP:0031186" + ], + "abnormal circulating deoxycorticosterone level": [ + "HP:0031186" + ], + "abnormal circulate pregnenolone concentration": [ + "HP:0031187" + ], + "abnormal circulating pregnenolone concentration": [ + "HP:0031187" + ], + "abnormality of circulate pregnenolone level": [ + "HP:0031187" + ], + "abnormality of circulating pregnenolone level": [ + "HP:0031187" + ], + "genital edema": [ + "HP:0031188" + ], + "genital oedema": [ + "HP:0031188" + ], + "wrist drop": [ + "HP:0031189" + ], + "superficial dermal perivascular inflammatory infiltrate": [ + "HP:0031190" + ], + "superficial perivascular inflammatory infiltrate": [ + "HP:0031190" + ], + "deep dermal perivascular inflammatory infiltrate": [ + "HP:0031191" + ], + "deep perivascular inflammatory infiltrate": [ + "HP:0031191" + ], + "abnormal morphology of left ventricular trabecula": [ + "HP:0031192" + ], + "abnormal morphology of left ventricular trabeculae": [ + "HP:0031192" + ], + "abnormal morphology 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"granular cast": [ + "HP:0031201" + ], + "granular casts": [ + "HP:0031201" + ], + "waxy cast": [ + "HP:0031202" + ], + "waxy casts": [ + "HP:0031202" + ], + "fatty cast": [ + "HP:0031203" + ], + "fatty casts": [ + "HP:0031203" + ], + "bacterial cell cast": [ + "HP:0031204" + ], + "bacterial cell casts": [ + "HP:0031204" + ], + "reduce lysosomal acid lipase activity": [ + "HP:0031205" + ], + "reduced lysosomal acid lipase activity": [ + "HP:0031205" + ], + "reduce leukocyte acid lipase activity": [ + "HP:0031205" + ], + "reduced leukocyte acid lipase activity": [ + "HP:0031205" + ], + "striatal t2 hyperintensity": [ + "HP:0031206" + ], + "hepatic hemangioma": [ + "HP:0031207" + ], + "hemangioma of the liver": [ + "HP:0031207" + ], + "liver hemangioma": [ + "HP:0031207" + ], + "increase pituitary glycoprotein hormone alpha subunit level": [ + "HP:0031208" + ], + "increased pituitary glycoprotein hormone alpha subunit level": [ + "HP:0031208" + ], + "increase pituitary glycoprotein alpha subunit level": [ + "HP:0031208" + ], + "increased pituitary glycoprotein alpha subunit level": [ + "HP:0031208" + ], + "increase pituitary glycoprotein polypeptide alpha subunit level": [ + "HP:0031208" + ], + "increased pituitary glycoprotein polypeptide alpha subunit level": [ + "HP:0031208" + ], + "decrease circulate lipoprotein lipase concentration": [ + "HP:0031209" + ], + "decreased circulating lipoprotein lipase concentration": [ + "HP:0031209" + ], + "decrease lipoprotein lipase level": [ + "HP:0031209" + ], + "decreased lipoprotein lipase level": [ + "HP:0031209" + ], + "abnormal circulate hyaluronic acid concentration": [ + "HP:0031210" + ], + "abnormal circulating hyaluronic acid concentration": [ + "HP:0031210" + ], + "elevate cholesterol ester level": [ + "HP:0031211" + ], + "elevated cholesterol ester level": [ + "HP:0031211" + ], + "elevate cholesteryl ester level": [ + "HP:0031211" + ], + "elevated cholesteryl ester level": [ + "HP:0031211" + ], + "increase cholesterol ester": [ + "HP:0031211" + ], + "increased cholesterol esters": [ + "HP:0031211" + ], + "increase cholesteryl ester": [ + "HP:0031211" + ], + "increased cholesteryl esters": [ + "HP:0031211" + ], + "abnormal circulate progesterone level": [ + "HP:0031212" + ], + "abnormal circulating progesterone level": [ + "HP:0031212" + ], + "elevate circulate 17 - hydroxyprogesterone": [ + "HP:0031213" + ], + "elevated circulating 17 - hydroxyprogesterone": [ + "HP:0031213" + ], + "elevate circulate 17 - ohp": [ + "HP:0031213" + ], + "elevated circulating 17 - ohp": [ + "HP:0031213" + ], + "decrease circulate dehydroepiandrosterone concentration": [ + "HP:0031214" + ], + "decreased circulating dehydroepiandrosterone concentration": [ + "HP:0031214" + ], + "decrease circulate dehydroepiandrosterone level": [ + "HP:0031214" + ], + "decreased circulating dehydroepiandrosterone level": [ + "HP:0031214" + ], + "decrease circulate dehydroepiandrosterone - sulfate concentration": [ + "HP:0031215" + ], + "decreased circulating dehydroepiandrosterone - sulfate concentration": [ + "HP:0031215" + ], + "decrease circulate dehydroepiandrosterone - sulfate level": [ + "HP:0031215" + ], + "decreased circulating dehydroepiandrosterone - sulfate level": [ + "HP:0031215" + ], + "increase circulate progesterone": [ + "HP:0031216" + ], + "increased circulating progesterone": [ + "HP:0031216" + ], + "hot flash": [ + "HP:0031217" + ], + "hot flashes": [ + "HP:0031217" + ], + "inappropriate antidiuretic hormone secretion": [ + "HP:0031218" + ], + "inappropriate adh secretion": [ + "HP:0031218" + ], + "syndrome of inappropriate antidiuretic hormone secretion": [ + "HP:0031218" + ], + "reduce radioactive iodine uptake": [ + "HP:0031219" + ], + "reduced radioactive iodine uptake": [ + "HP:0031219" + ], + "increase radioactive iodine uptake": [ + "HP:0031220" + ], + "increased radioactive iodine uptake": [ + "HP:0031220" + ], + "abnormal radioactive iodine uptake test result": [ + "HP:0031221" + ], + "increase circulate thyroxine - binding globulin level": [ + "HP:0031222" + ], + "increased circulating thyroxine - binding globulin level": [ + "HP:0031222" + ], + "focal pancreatic islet hyperplasia": [ + "HP:0031223" + ], + "diffuse pancreatic islet hyperplasia": [ + "HP:0031224" + ], + "intrapulmonary shunt": [ + "HP:0031225" + ], + "intrapulmonary shunting": [ + "HP:0031225" + ], + "perinephric fluid collection": [ + "HP:0031226" + ], + "nasopharyngeal teratoma": [ + "HP:0031227" + ], + "abnormal incisura morphology": [ + "HP:0031228" + ], + "increase incisura length": [ + "HP:0031229" + ], + "increased incisura length": [ + "HP:0031229" + ], + "decrease incisura length": [ + "HP:0031230" + ], + "decreased incisura length": [ + "HP:0031230" + ], + "narrow incisura width": [ + "HP:0031231" + ], + "increase incisura width": [ + "HP:0031232" + ], + "increased incisura width": [ + "HP:0031232" + ], + "horizontal inferior border of scapula": [ + "HP:0031233" + ], + "squaring of the inferior scapula": [ + "HP:0031233" + ], + "squaring of the inferior scapulae": [ + "HP:0031233" + ], + "squaring of the scapula": [ + "HP:0031233" + ], + "neutrophilic infiltration of the skin": [ + "HP:0031234" + ], + "predominantly epidermal neutrophilic infiltrate": [ + "HP:0031235" + ], + "predominantly dermal neutrophilic infiltrate": [ + "HP:0031236" + ], + "internally nucleated skeletal muscle fiber": [ + "HP:0031237" + ], + "internally nucleated skeletal muscle fibers": [ + "HP:0031237" + ], + "internally nucleated skeletal muscle fibre": [ + "HP:0031237" + ], + "internally nucleated skeletal muscle fibres": [ + "HP:0031237" + ], + "necklace skeletal muscle fiber": [ + "HP:0031238" + ], + "necklace skeletal muscle fibers": [ + "HP:0031238" + ], + "necklace skeletal muscle fibre": [ + "HP:0031238" + ], + "necklace skeletal muscle fibres": [ + "HP:0031238" + ], + "extrafoveal choroidal neovascularization": [ + "HP:0031239" + ], + "juxtafoveal choroidal neovascularization": [ + 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cough": [ + "HP:0031246" + ], + "dry cough": [ + "HP:0031246" + ], + "dry coughing": [ + "HP:0031246" + ], + "whooping cough": [ + "HP:0031247" + ], + "palmar pruritus": [ + "HP:0031248" + ], + "itchy palm": [ + "HP:0031248" + ], + "parageusia": [ + "HP:0031249" + ], + "altered sense of taste": [ + "HP:0031249" + ], + "dysgeusia": [ + "HP:0031249" + ], + "metallic taste": [ + "HP:0031249" + ], + "metallic taste in mouth": [ + "HP:0031249" + ], + "lip fissure": [ + "HP:0031250" + ], + "abnormal subclavian artery morphology": [ + "HP:0031251" + ], + "dilate leave subclavian artery": [ + "HP:0031252" + ], + "dilated left subclavian artery": [ + "HP:0031252" + ], + "anomalous origin of left subclavian artery": [ + "HP:0031253" + ], + "thalamic arteriovenous malformation": [ + "HP:0031254" + ], + "hypothalamic arteriovenous malformation": [ + "HP:0031255" + ], + "optic nerve arteriovenous malformation": [ + "HP:0031256" + ], + "arteriovenous malformation of the maxilla": [ + "HP:0031257" + ], + "delirium": [ + "HP:0031258" + ], + "oophoritis": [ + "HP:0031259" + ], + "inflammed ovary": [ + "HP:0031259" + ], + "triangular tibia": [ + "HP:0031260" + ], + "bladder polyp": [ + "HP:0031261" + ], + "abnormal renal corpuscle morphology": [ + "HP:0031263" + ], + "abnormal bowman capsule morphology": [ + "HP:0031264" + ], + "abnormal morphology of bowman capsule": [ + "HP:0031264" + ], + "abnormal morphology of bowman 's capsule": [ + "HP:0031264" + ], + "abnormal renal glomerular capsule morphology": [ + "HP:0031264" + ], + "abnormal glomerular visceral epithelial cell morphology": [ + "HP:0031265" + ], + "abnormal podocyte morphology": [ + "HP:0031265" + ], + "abnormal visceral epithelial cell morphology": [ + "HP:0031265" + ], + "podocyte foot process effacement": [ + "HP:0031266" + ], + "loss of primary podocyte process": [ + "HP:0031266" + ], + "loss of primary podocyte processes": [ + "HP:0031266" + ], + "abnormal cd69 upregulation upon tcr activation": [ + "HP:0031267" + ], + "decrease cd69 upregulation upon tcr activation": [ + "HP:0031268" + ], + "decreased cd69 upregulation upon tcr activation": [ + "HP:0031268" + ], + "abnormal cd25 upregulation upon tcr activation": [ + "HP:0031269" + ], + "decrease cd25 upregulation upon tcr activation": [ + "HP:0031270" + ], + "decreased cd25 upregulation upon tcr activation": [ + "HP:0031270" + ], + "poor cd25 upregulation upon tcr activation": [ + "HP:0031270" + ], + "reduce il2ra upregulation upon tcr activation": [ + "HP:0031270" + ], + "reduced il2ra upregulation upon tcr activation": [ + "HP:0031270" + ], + "absent ankle pulse": [ + "HP:0031271" + ], + "pulmonary arterial atherosclerosis": [ + "HP:0031272" + ], + "shock": [ + "HP:0031273" + ], + "hypovolemic shock": [ + "HP:0031274" + ], + "distributive shock": [ + "HP:0031275" + ], + "obstructive shock": [ + "HP:0031276" + ], + "abnormal thoracic duct morphology": [ + "HP:0031278" + ], + "abnormal response to gonadotropin - release hormone stimulation test": [ + "HP:0031279" + ], + "abnormal response to gonadotropin - releasing hormone stimulation test": [ + "HP:0031279" + ], + "abnormal response to gnrh stimulation test": [ + "HP:0031279" + ], + "increase lh response to gonadotropin - release hormone stimulation test": [ + "HP:0031280" + ], + "increased lh response to gonadotropin - releasing hormone stimulation test": [ + "HP:0031280" + ], + "sialadenitis": [ + "HP:0031281" + ], + "malalignment of the great toenail": [ + "HP:0031282" + ], + "tufted hair": [ + "HP:0031283" + ], + "tufted hairs": [ + "HP:0031283" + ], + "flush": [ + "HP:0031284" + ], + "flushing": [ + "HP:0031284" + ], + "abnormal perifollicular morphology": [ + "HP:0031285" + ], + "perifollicular erythema": [ + "HP:0031286" + ], + "seborrheic keratosis": [ + "HP:0031287" + ], + "basal cell papilloma": [ + "HP:0031287" + ], + "seborrheic verruca": [ + "HP:0031287" + ], + "senile wart": [ + "HP:0031287" + ], + "cobblestone - like hyperkeratosis": [ + "HP:0031288" + ], + "white papule": [ + "HP:0031289" + ], + "tuberous xanthoma": [ + "HP:0031290" + ], + "ichthyosis follicularis": [ + "HP:0031291" + ], + "cutaneous abscess": [ + "HP:0031292" + ], + "skin abscess": [ + "HP:0031292" + ], + "digital pitting scar": [ + "HP:0031293" + ], + "hypoplastic right atrium": [ + "HP:0031294" + ], + "leave atrial enlargement": [ + "HP:0031295" + ], + "left atrial enlargement": [ + "HP:0031295" + ], + "enlarged heart leave atrium": [ + "HP:0031295" + ], + "enlarged heart left atrium": [ + "HP:0031295" + ], + "atrial septal hypertrophy": [ + "HP:0031296" + ], + "unroofed coronary sinus": [ + "HP:0031297" + ], + "coronary sinus enlargement": [ + "HP:0031298" + ], + "coronary sinus dilatation": [ + "HP:0031298" + ], + "enlarge coronary sinus": [ + "HP:0031298" + ], + "enlarged coronary sinus": [ + "HP:0031298" + ], + "elevate leave atrial pressure": [ + "HP:0031299" + ], + "elevated left atrial pressure": [ + "HP:0031299" + ], + "abnormal circulate properdin level": [ + "HP:0031300" + ], + "abnormal circulating properdin level": [ + "HP:0031300" + ], + "peripheral arterial calcification": [ + "HP:0031301" + ], + "peripheral artery calcification": [ + "HP:0031301" + ], + "low extremity peripheral arterial calcification": [ + "HP:0031302" + ], + "lower extremity peripheral arterial calcification": [ + "HP:0031302" + ], + "low extremity peripheral artery calcification": [ + "HP:0031302" + ], + "lower extremity peripheral artery calcification": [ + "HP:0031302" + ], + "femoral arterial calcification": [ + "HP:0031303" + ], + "iliac arterial calcification": [ + "HP:0031304" + ], + "tibial arterial calcification": [ + "HP:0031305" + ], + "intracranial arterial calcification": [ + "HP:0031306" + ], + "internal carotid artery calcification": [ + "HP:0031307" + ], + "vertebral artery calcification": [ + "HP:0031308" + ], + "cerebral artery calcification": [ + "HP:0031309" + ], + "basilar artery calcification": [ + "HP:0031310" + ], + "middle cerebral artery calcification": [ + "HP:0031311" + ], + "abdominal aortic calcification": [ + "HP:0031313" + ], + "carotid artery calcification": [ + "HP:0031314" + ], + "external carotid artery calcification": [ + "HP:0031315" + ], + "abnormal ventricular myocardium morphology": [ + "HP:0031316" + ], + "fatty replacement of ventricular myocardial tissue": [ + "HP:0031317" + ], + "fatty infiltration of cardiac ventricle": [ + "HP:0031317" + ], + "intramyocardial fat infiltration": [ + "HP:0031317" + ], + "myofiber disarray": [ + "HP:0031318" + ], + "myocardial fiber disarray": [ + "HP:0031318" + ], + "myocardial fibre disarray": [ + "HP:0031318" + ], + "cardiomyocyte hypertrophy": [ + "HP:0031319" + ], + "myocyte cellular hypertrophy": [ + "HP:0031319" + ], + "cardiomyocyte mitochondrial proliferation": [ + "HP:0031320" + ], + "myocardial immune cell infiltration": [ + "HP:0031321" + ], + "myocardial lymphocytic infiltration": [ + "HP:0031322" + ], + "myocardial eosinophilic infiltration": [ + "HP:0031323" + ], + "myocardial multinucleated giant cell": [ + "HP:0031324" + ], + "myocardial multinucleated giant cells": [ + "HP:0031324" + ], + "myocardial granulomatous infiltrates": [ + "HP:0031325" + ], + "monoclonal light chain cardiac amyloidosis": [ + "HP:0031326" + ], + "transthyretin cardiac amyloidosis": [ + "HP:0031327" + ], + "ttr cardiac amyloidosis": [ + "HP:0031327" + ], + "perivascular cardiac fibrosis": [ + "HP:0031328" + ], + "interstitial cardiac fibrosis": [ + "HP:0031329" + ], + "perivascular myocardial immune cell infiltration": [ + "HP:0031330" + ], + "abnormal cardiomyocyte morphology": [ + "HP:0031331" + ], + "abnormal cardiac muscle cell morphology": [ + "HP:0031331" + ], + "cardiomyocyte degeneration": [ + "HP:0031332" + ], + "myocardial sarcomeric disarray": [ + "HP:0031333" + ], + "myocardial sarcomere disarray": [ + "HP:0031333" + ], + "cardiomyocyte inclusion body": [ + "HP:0031334" + ], + "cardiomyocyte inclusion bodies": [ + "HP:0031334" + ], + "abnormal cardiomyocyte mitochondrial morphology": [ + "HP:0031335" + ], + "intranuclear cardiomyocyte mitochondrion": [ + "HP:0031336" + ], + "intranuclear cardiomyocyte mitochondria": [ + "HP:0031336" + ], + "abnormal cardiomyocyte connexin43 stain": [ + "HP:0031337" + ], + "abnormal cardiomyocyte connexin43 staining": [ + "HP:0031337" + ], + "abnormal cardiomyocyte plakoglobin stain": [ + "HP:0031338" + ], + "abnormal cardiomyocyte plakoglobin staining": [ + "HP:0031338" + ], + "abnormal cadiomyocyte dystrophin stain": [ + "HP:0031339" + ], + "abnormal cadiomyocyte dystrophin staining": [ + "HP:0031339" + ], + "abnormal lysosomal morphology": [ + "HP:0031340" + ], + "gastric arteriovenous malformation": [ + "HP:0031341" + ], + "duodenal arteriovenous malformation": [ + "HP:0031342" + ], + "jejunal arteriovenous malformation": [ + "HP:0031343" + ], + "pelvic arteriovenous malformation": [ + "HP:0031344" + ], + "colonic arteriovenous malformation": [ + "HP:0031345" + ], + "rectal arteriovenous malformation": [ + "HP:0031346" + ], + "uterine arteriovenous malformation": [ + "HP:0031347" + ], + "dextrotransposition of the great artery": [ + "HP:0031348" + ], + "dextrotransposition of the great arteries": [ + "HP:0031348" + ], + "d - loop transposition of the great artery": [ + "HP:0031348" + ], + "d - loop transposition of the great arteries": [ + "HP:0031348" + ], + "levotransposition of the great artery": [ + "HP:0031349" + ], + "levotransposition of the great arteries": [ + "HP:0031349" + ], + "cardiac sarcoma": [ + "HP:0031350" + ], + "calcify amorphous tumor of the heart": [ + "HP:0031351" + ], + "calcified amorphous tumor of the heart": [ + "HP:0031351" + ], + "calcify amorphous tumour of the heart": [ + "HP:0031351" + ], + "calcified amorphous tumour of the heart": [ + "HP:0031351" + ], + "chest tightness": [ + "HP:0031352" + ], + "chest distress": [ + "HP:0031352" + ], + "tightness in chest": [ + "HP:0031352" + ], + "tightness of chest": [ + "HP:0031352" + ], + "otitis medium with effusion": [ + "HP:0031353" + ], + "otitis media with effusion": [ + "HP:0031353" + ], + "fluid behind eardrum": [ + "HP:0031353" + ], + "sleep onset insomnia": [ + "HP:0031354" + ], + "difficulty fall asleep": [ + "HP:0031354" + ], + "difficulty falling asleep": [ + "HP:0031354" + ], + "maintenance insomnia": [ + "HP:0031355" + ], + "wake up several time during the night": [ + "HP:0031355" + ], + "waking up several times during the night": [ + "HP:0031355" + ], + "terminal insomnia": [ + "HP:0031356" + ], + "late insomnia": [ + "HP:0031356" + ], + "glomeruloid hemangioma": [ + "HP:0031357" + ], + "vegetative state": [ + "HP:0031358" + ], + "cutaneous sclerotic plaque": [ + "HP:0031359" + ], + "yellow skin plaque": [ + "HP:0031360" + ], + "zebra body": [ + "HP:0031361" + ], + "zebra bodies": [ + "HP:0031361" + ], + "sex - limited autosomal recessive inheritance": [ + "HP:0031362" + ], + "palpable purpura": [ + "HP:0031363" + ], + "ecchymosis": [ + "HP:0031364" + ], + "ecchymoses": [ + "HP:0031364" + ], + "macular purpura": [ + "HP:0031365" + ], + "flat purpura": [ + "HP:0031365" + ], + "palate neoplasm": [ + "HP:0031366" + ], + "metaphyseal striation": [ + "HP:0031367" + ], + "metaphyseal striations": [ + "HP:0031367" + ], + "striate metaphysis": [ + "HP:0031367" + ], + "striated metaphysis": [ + "HP:0031367" + ], + "intestinal perforation": [ + "HP:0031368" + ], + "colon perforation": [ + "HP:0031369" + ], + "perforation of the colon": [ + "HP:0031369" + ], + "small intestinal perforation": [ + "HP:0031370" + ], + "rectal perforation": [ + "HP:0031371" + ], + "cold paresis": [ + "HP:0031372" + ], + "stiff tongue": [ + "HP:0031373" + ], + "tongue stiffness": [ + "HP:0031373" + ], + "ankle weakness": [ + "HP:0031374" + ], + "refractory": [ + "HP:0031375" + ], + "abnormal cell proliferation": [ + "HP:0031377" + ], + "abnormal lymphocyte proliferation": [ + "HP:0031378" + ], + "abnormal t cell proliferation": [ + "HP:0031379" + ], + "abnormal b cell proliferation": [ + "HP:0031380" + ], + "decrease lymphocyte proliferation in response to mitogen": [ + "HP:0031381" + ], + "decreased lymphocyte proliferation in response to mitogen": [ + "HP:0031381" + ], + "reduce lymphocyte proliferation to mitogen": [ + "HP:0031381" + ], + "reduced lymphocyte proliferation to mitogen": [ + "HP:0031381" + ], + "decrease lymphocyte proliferation in response to anti - cd3": [ + "HP:0031382" + ], + "decreased lymphocyte proliferation in response to anti - cd3": [ + "HP:0031382" + ], + "defective lymphocyte proliferation to anti - cd3": [ + "HP:0031382" + ], + "defective proliferation of lymphocyte follow anti - cd3 stimulation": [ + "HP:0031382" + ], + "defective proliferation of lymphocytes following anti - cd3 stimulation": [ + "HP:0031382" + ], + "abnormal lymphocyte surface marker expression": [ + "HP:0031383" + ], + "reduce t cell cd40 expression": [ + "HP:0031384" + ], + "reduced t cell cd40 expression": [ + "HP:0031384" + ], + "megakaryocyte nucleus hypolobulation": [ + "HP:0031385" + ], + "increase micromegakaryocyte count": [ + "HP:0031386" + ], + "increased micromegakaryocyte count": [ + "HP:0031386" + ], + "increase multinucleated megakaryocyte count": [ + "HP:0031387" + ], + "increased multinucleated megakaryocyte count": [ + "HP:0031387" + ], + "megakaryocyte nucleus hyperlobulation": [ + "HP:0031388" + ], + "abnormal mhc ii surface expression": [ + "HP:0031389" + ], + "reduce mhc ii surface expression": [ + "HP:0031390" + ], + "reduced mhc ii surface expression": [ + "HP:0031390" + ], + "elevate mhc ii surface expression": [ + "HP:0031391" + ], + "elevated mhc ii surface expression": [ + "HP:0031391" + ], + "abnormal proportion of cd4 - positive t cell": [ + "HP:0031392" + ], + "abnormal proportion of cd4 - positive t cells": [ + "HP:0031392" + ], + "abnormal proportion of cd4+ t cell": [ + "HP:0031392" + ], + "abnormal proportion of cd4+ t cells": [ + "HP:0031392" + ], + "abnormal proportion of cd4 - positive , alpha - beta t cell": [ + "HP:0031392" + ], + "abnormal proportion of cd4 - positive , alpha - beta t cells": [ + "HP:0031392" + ], + "abnormal proportion of cd8 - positive t cell": [ + "HP:0031393" + ], + "abnormal proportion of cd8 - positive t cells": [ + "HP:0031393" + ], + "abnormal proportion of cd8+ t cell": [ + "HP:0031393" + ], + "abnormal proportion of cd8+ t cells": [ + "HP:0031393" + ], + "abnormal proportion of cd8 - positive , alpha - beta t cell": [ + "HP:0031393" + ], + "abnormal proportion of cd8 - positive , alpha - beta t cells": [ + "HP:0031393" + ], + "abnormal cd4 : cd8 ratio": [ + "HP:0031394" + ], + "abnormal proportion of naive t cell": [ + "HP:0031396" + ], + "abnormal proportion of naive t cells": [ + "HP:0031396" + ], + "abnormal naive t cell proportion": [ + "HP:0031396" + ], + "abnormal proportion of naive thymus - derive , alpha - beta t cell": [ + "HP:0031396" + ], + "abnormal proportion of naive thymus - derived , alpha - beta t cells": 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"HP:0031399" + ], + "abnormal cd4 - negative , cd8 - negative , alpha - beta regulatory t cell distribution": [ + "HP:0031399" + ], + "abnormal dn treg distribution": [ + "HP:0031399" + ], + "abnormal double negative treg distribution": [ + "HP:0031399" + ], + "abnormal double - negative alpha - beta regulatory t cell distribution": [ + "HP:0031399" + ], + "reduce proportion of cd4 - negative , cd8 - negative , alpha - beta regulatory t cell": [ + "HP:0031401" + ], + "reduced proportion of cd4 - negative , cd8 - negative , alpha - beta regulatory t cells": [ + "HP:0031401" + ], + "reduce antigen - specific t cell proliferation": [ + "HP:0031402" + ], + "reduced antigen - specific t cell proliferation": [ + "HP:0031402" + ], + "antigen - specific t cell proliferation defect": [ + "HP:0031402" + ], + "impaired activate t cell proliferation": [ + "HP:0031402" + ], + "impaired activated t cell proliferation": [ + "HP:0031402" + ], + "impaired ag - specific t cell proliferation": [ + "HP:0031402" + ], + "impaired cellular adaptive immune response": [ + "HP:0031402" + ], + "impaired pathogen - specific cd8 cytoxicity": [ + "HP:0031403" + ], + "pathogen - specific cd8 cytoxicity defect": [ + "HP:0031403" + ], + "impaired antigen - specific response": [ + "HP:0031404" + ], + "impaired adaptive immune response": [ + "HP:0031404" + ], + "poroma": [ + "HP:0031405" + ], + "abnormal cytokine signal": [ + "HP:0031406" + ], + "abnormal cytokine signaling": [ + "HP:0031406" + ], + "abnormal cytokine signalling": [ + "HP:0031406" + ], + "impaired cytokine signal": [ + "HP:0031407" + ], + "impaired cytokine signaling": [ + "HP:0031407" + ], + "cytokine signal defect": [ + "HP:0031407" + ], + "cytokine signaling defect": [ + "HP:0031407" + ], + "cytokine signalling defect": [ + "HP:0031407" + ], + "impaired cytokine signalling": [ + "HP:0031407" + ], + "increase proportion of cd25+ mast cell": [ + "HP:0031408" + ], + "increased proportion of cd25+ mast cells": [ + "HP:0031408" + ], + "abnormal lymphocyte physiology": [ + "HP:0031409" + ], + "abnormal distribution of cd56 bright / dim natural killer cell": [ + "HP:0031410" + ], + "abnormal distribution of cd56 bright / dim natural killer cells": [ + "HP:0031410" + ], + "abnormal distribution of cd56 bright / dim nk cell": [ + "HP:0031410" + ], + "abnormal distribution of cd56 bright / dim nk cells": [ + "HP:0031410" + ], + "abnormal chromosome morphology": [ + "HP:0031411" + ], + "abnormal telomere morphology": [ + "HP:0031412" + ], + "short telomere length": [ + "HP:0031413" + ], + "high serum calcifediol": [ + "HP:0031414" + ], + "high serum 25 - hydroxycholecalciferol": [ + "HP:0031414" + ], + "high serum calcidiol": [ + "HP:0031414" + ], + "high serum calcitriol": [ + "HP:0031415" + ], + "high serum 1,25 - dihydroxycholecalciferol": [ + "HP:0031415" + ], + "high serum 1,25 - dihydroxyvitamin d3": [ + "HP:0031415" + ], + "increase serum 1,25 - dihydroxyvitamin d3": [ + "HP:0031415" + ], + "increased serum 1,25 - dihydroxyvitamin d3": [ + "HP:0031415" + ], + "increase serum calcitriol": [ + "HP:0031415" + ], + "increased serum calcitriol": [ + "HP:0031415" + ], + "abnormal nasal mucus secretion": [ + "HP:0031416" + ], + "rhinorrhea": [ + "HP:0031417" + ], + "nasal discharge": [ + "HP:0031417" + ], + "runny nose": [ + "HP:0031417" + ], + "increase body mass index": [ + "HP:0031418" + ], + "increased body mass index": [ + "HP:0031418" + ], + "increase bmi": [ + "HP:0031418" + ], + "increased bmi": [ + "HP:0031418" + ], + "reduce sex - hormone bind protein level": [ + "HP:0031419" + ], + "reduced sex - hormone binding protein level": [ + "HP:0031419" + ], + "reduce androgen - bind protein level": [ + "HP:0031419" + ], + "reduced androgen - binding protein level": [ + "HP:0031419" + ], + "small yellow foveal lesion with surround gray zone": [ + "HP:0031420" + ], + "small yellow foveal lesion with surrounding gray zone": [ + "HP:0031420" + ], + "laser pointer - induce maculopathy": [ + "HP:0031420" + ], + "laser pointer - induced maculopathy": [ + "HP:0031420" + ], + "laser pointer - induce retinopathy": [ + "HP:0031420" + ], + "laser pointer - induced retinopathy": [ + "HP:0031420" + ], + "light induce retinopathy": [ + "HP:0031420" + ], + "light induced retinopathy": [ + "HP:0031420" + ], + "photic retinopathy": [ + "HP:0031420" + ], + "small yellow foveal lesion with surround grey zone": [ + "HP:0031420" + ], + "small yellow foveal lesion with surrounding grey zone": [ + "HP:0031420" + ], + "solar retinitis": [ + "HP:0031420" + ], + "solar retinopathy": [ + "HP:0031420" + ], + "small superior frontal cortex": [ + "HP:0031421" + ], + "abnormal cerebellar cortex morphology": [ + "HP:0031422" + ], + "abnormal morphology of the cerebellar cortex": [ + "HP:0031422" + ], + "small cerebellar cortex": [ + "HP:0031423" + ], + "abnormal circulate beta - c - terminal telopeptide level": [ + "HP:0031424" + ], + "abnormal circulating beta - c - terminal telopeptide level": [ + "HP:0031424" + ], + "abnormal circulate beta - crosslaps level": [ + "HP:0031424" + ], + "abnormal circulating beta - crosslaps level": [ + "HP:0031424" + ], + "abnormal circulate beta - ctx level": [ + "HP:0031424" + ], + "abnormal circulating beta - ctx level": [ + "HP:0031424" + ], + "increase circulate beta - c - terminal telopeptide level": [ + "HP:0031425" + ], + "increased circulating beta - c - terminal telopeptide level": [ + "HP:0031425" + ], + "increase circulate beta - crosslaps level": [ + "HP:0031425" + ], + "increased circulating beta - crosslaps level": [ + "HP:0031425" + ], + "increase circulate beta - ctx level": [ + "HP:0031425" + ], + "increased circulating beta - ctx level": [ + "HP:0031425" + ], + "decrease circulate beta - c - terminal telopeptide level": [ + "HP:0031426" + ], + "decreased circulating beta - c - terminal telopeptide level": [ + "HP:0031426" + ], + "decrease circulate beta - crosslaps level": [ + "HP:0031426" + ], + "decreased circulating beta - crosslaps level": [ + "HP:0031426" + ], + "decrease circulate beta - ctx level": [ + "HP:0031426" + ], + "decreased circulating beta - ctx level": [ + "HP:0031426" + ], + "abnormal circulate osteocalcin level": [ + "HP:0031427" + ], + "abnormal circulating osteocalcin level": [ + "HP:0031427" + ], + "increase circulate osteocalcin level": [ + "HP:0031428" + ], + "increased circulating osteocalcin level": [ + "HP:0031428" + ], + "decrease circulate osteocalcin level": [ + "HP:0031429" + ], + "decreased circulating osteocalcin level": [ + "HP:0031429" + ], + "oligoclonal t cell expansion": [ + "HP:0031430" + ], + "persistent repetition of word": [ + "HP:0031431" + ], + "persistent repetition of words": [ + "HP:0031431" + ], + "persistent repetition of action": [ + "HP:0031432" + ], + "persistent repetition of actions": [ + "HP:0031432" + ], + "alexithymia": [ + "HP:0031433" + ], + "unaware of others ' emotion": [ + "HP:0031433" + ], + "unaware of others ' emotions": [ + "HP:0031433" + ], 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with follicular differentiation": [ + "HP:0031548" + ], + "follicular infundibulum tumour": [ + "HP:0031548" + ], + "lymphocytoma cutis": [ + "HP:0031549" + ], + "skin pseudolymphoma": [ + "HP:0031549" + ], + "spiegler - fendt sarcoid": [ + "HP:0031549" + ], + "abnormal flow cytometry test result": [ + "HP:0031550" + ], + "reduce cell surface marker level": [ + "HP:0031551" + ], + "reduced cell surface marker level": [ + "HP:0031551" + ], + "reduce fibroblast surface marker level": [ + "HP:0031552" + ], + "reduced fibroblast surface marker level": [ + "HP:0031552" + ], + "reduce granulocyte surface marker level": [ + "HP:0031553" + ], + "reduced granulocyte surface marker level": [ + "HP:0031553" + ], + "reduce granulocyte cd55 level": [ + "HP:0031554" + ], + "reduced granulocyte cd55 level": [ + "HP:0031554" + ], + "reduce granulocyte cd59 level": [ + "HP:0031555" + ], + "reduced granulocyte cd59 level": [ + "HP:0031555" + ], + "reduce granulocyte cd16 level": [ + "HP:0031556" + ], + "reduced granulocyte cd16 level": [ + "HP:0031556" + ], + "reduce fibroblast cd55 level": [ + "HP:0031557" + ], + "reduced fibroblast cd55 level": [ + "HP:0031557" + ], + "reduce fibroblast cd59 level": [ + "HP:0031558" + ], + "reduced fibroblast cd59 level": [ + "HP:0031558" + ], + "reduce fibroblast cd16 level": [ + "HP:0031559" + ], + "reduced fibroblast cd16 level": [ + "HP:0031559" + ], + "coronary cameral fistula": [ + "HP:0031560" + ], + "coronary cameral fistula to right ventricle": [ + "HP:0031561" + ], + "balance double aortic arch": [ + "HP:0031562" + ], + "balanced double aortic arch": [ + "HP:0031562" + ], + "coronary arteriovenous fistula": [ + "HP:0031563" + ], + "bronchial isomerism": [ + "HP:0031564" + ], + "abdominal situs ambiguus": [ + "HP:0031565" + ], + "abnormal pulmonary valve cusp morphology": [ + "HP:0031566" + ], + "abnormal aortic valve cusp morphology": [ + "HP:0031567" + ], + "thicken aortic valve cusp": [ + "HP:0031568" + ], + "thickened aortic valve cusp": [ + "HP:0031568" + ], + "absent aortic valve cusp": [ + "HP:0031569" + ], + "absent aortic valve cusps": [ + "HP:0031569" + ], + "absent aortic valve": [ + "HP:0031569" + ], + "tessier number 0 facial cleft": [ + "HP:0031570" + ], + "tessier facial cleft number 0": [ + "HP:0031570" + ], + "paramedian facial cleft": [ + "HP:0031571" + ], + "tessier number 1 facial cleft": [ + "HP:0031572" + ], + "tessier number 2 facial cleft": [ + "HP:0031573" + ], + "orbital cleft": [ + "HP:0031574" + ], + "tessier number 3 facial cleft": [ + "HP:0031575" + ], + "tessier number 4 facial cleft": [ + "HP:0031576" + ], + "tessier number 5 facial cleft": [ + "HP:0031577" + ], + "tessier number 6 facial cleft": [ + "HP:0031578" + ], + "tessier facial cleft number 6": [ + "HP:0031578" + ], + "tessier number 7 facial cleft": [ + "HP:0031579" + ], + "tessier cleave number 7": [ + "HP:0031579" + ], + "tessier cleft number 7": [ + "HP:0031579" + ], + "tessier facial cleft number 7": [ + "HP:0031579" + ], 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"HP:0031603" + ], + "agenesis of the carotid canal": [ + "HP:0031604" + ], + "bony carotid canal agenesis": [ + "HP:0031604" + ], + "abnormality of fundus pigmentation": [ + "HP:0031605" + ], + "retinal cotton wool spot": [ + "HP:0031606" + ], + "pelvic organ prolapse": [ + "HP:0031607" + ], + "geographic atrophy": [ + "HP:0031609" + ], + "recurrent shoulder dislocation": [ + "HP:0031610" + ], + "multiple shoulder dislocation": [ + "HP:0031610" + ], + "sub - inner limit membrane hemorrhage": [ + "HP:0031611" + ], + "sub - inner limiting membrane hemorrhage": [ + "HP:0031611" + ], + "sub - ilm haemorrhage": [ + "HP:0031611" + ], + "sub - ilm hemorrhage": [ + "HP:0031611" + ], + "sub - inner limit membrane haemorrhage": [ + "HP:0031611" + ], + "sub - inner limiting membrane haemorrhage": [ + "HP:0031611" + ], + "inferior chorioretinal coloboma": [ + "HP:0031613" + ], + "inferior retinal coloboma": [ + "HP:0031614" + ], + "hypopyon": [ + "HP:0031615" + ], + "anterior chamber flare": [ + 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"absent left main coronary artery": [ + "HP:0031639" + ], + "absent lmca": [ + "HP:0031639" + ], + "abnormal radial artery morphology": [ + "HP:0031640" + ], + "fusiform ascend tubular aorta aneurysm": [ + "HP:0031643" + ], + "fusiform ascending tubular aorta aneurysm": [ + "HP:0031643" + ], + "fusiform abdominal aortic aneurysm": [ + "HP:0031644" + ], + "saccular abdominal aortic aneurysm": [ + "HP:0031645" + ], + "fusiform aortic arch aneurysm": [ + "HP:0031646" + ], + "saccular aortic arch aneurysm": [ + "HP:0031647" + ], + "penetrate aortic ulcer": [ + "HP:0031648" + ], + "penetrating aortic ulcer": [ + "HP:0031648" + ], + "aortic rupture": [ + "HP:0031649" + ], + "abnormal atrioventricular valve physiology": [ + "HP:0031650" + ], + "abnormal tricuspid valve physiology": [ + "HP:0031651" + ], + "abnormal aortic valve physiology": [ + "HP:0031652" + ], + "abnormal heart valve physiology": [ + "HP:0031653" + ], + "abnormal pulmonary valve physiology": [ + "HP:0031654" + ], + 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infection": [ + "HP:0032261" + ], + "pulmonary tuberculosis": [ + "HP:0032262" + ], + "pulmonary tb": [ + "HP:0032262" + ], + "increase blood pressure": [ + "HP:0032263" + ], + "increased blood pressure": [ + "HP:0032263" + ], + "increase bp": [ + "HP:0032263" + ], + "increased bp": [ + "HP:0032263" + ], + "anti - nmda receptor antibody positivity": [ + "HP:0032264" + ], + "presence of anti - n - methyl - d - aspartate receptor antibody in blood": [ + "HP:0032264" + ], + "presence of anti - nmdar antibody in blood": [ + "HP:0032264" + ], + "csf autoimmune antibody positivity": [ + "HP:0032265" + ], + "cerebrospinal fluid autoimmune antibody positivity": [ + "HP:0032265" + ], + "csf anti - nmda receptor antibody positivity": [ + "HP:0032266" + ], + "presence of anti - n - methyl - d - aspartate receptor antibody in csf": [ + "HP:0032266" + ], + "presence of anti - nmdar antibody in cerebrospinal fluid": [ + "HP:0032266" + ], + "presence of nmdar antibody in csf": [ + "HP:0032266" + ], + 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fibronectin": [ + "HP:0032463" + ], + "ureteral hypoplasia": [ + "HP:0032464" + ], + "hypoplasia of the ureter": [ + "HP:0032464" + ], + "ureter hypoplasia": [ + "HP:0032464" + ], + "bladder trabeculation": [ + "HP:0032465" + ], + "trabecular bladder": [ + "HP:0032465" + ], + "aplasia of the olfactory bulb": [ + "HP:0032466" + ], + "aplastic olfactory bulb": [ + "HP:0032466" + ], + "olfactory bulb aplasia": [ + "HP:0032466" + ], + "past obstetric history": [ + "HP:0032467" + ], + "maternal medical history": [ + "HP:0032467" + ], + "history of stillbirth": [ + "HP:0032468" + ], + "anti - asialoglycoprotein receptor antibody positivity": [ + "HP:0032469" + ], + "monilethrix": [ + "HP:0032470" + ], + "focal polymicrogyria": [ + "HP:0032471" + ], + "abnormal urine urobilinogen level": [ + "HP:0032472" + ], + "decrease urine urobilinogen": [ + "HP:0032473" + ], + "decreased urine urobilinogen": [ + "HP:0032473" + ], + "6 - layer lissencephaly": [ + "HP:0032475" + ], + "6 - layered lissencephaly": [ + "HP:0032475" + ], + "abnormal circulate vitamin b6 level": [ + "HP:0032476" + ], + "abnormal circulating vitamin b6 level": [ + "HP:0032476" + ], + "elevate circulate vitamin b6 level": [ + "HP:0032477" + ], + "elevated circulating vitamin b6 level": [ + "HP:0032477" + ], + "lateral spinal meningocele": [ + "HP:0032478" + ], + "preimplantation lethality": [ + "HP:0032479" + ], + "preimplantation embryonic lethality": [ + "HP:0032479" + ], + "beta - aminoisobutyric aciduria": [ + "HP:0032480" + ], + "abnormal pituitary glycoprotein hormone alpha subunit level": [ + "HP:0032481" + ], + "decrease pituitary glycoprotein hormone alpha subunit level": [ + "HP:0032482" + ], + "decreased pituitary glycoprotein hormone alpha subunit level": [ + "HP:0032482" + ], + "decrease pituitary glycoprotein alpha subunit level": [ + "HP:0032482" + ], + "decreased pituitary glycoprotein alpha subunit level": [ + "HP:0032482" + ], + "decrease pituitary glycoprotein polypeptide alpha subunit level": [ + "HP:0032482" + ], + "decreased pituitary glycoprotein polypeptide alpha subunit level": [ + "HP:0032482" + ], + "obsolete abnormal fecal test result": [ + "HP:0032483" + ], + "elevated fecal sodium": [ + "HP:0032484" + ], + "elevated faecal sodium": [ + "HP:0032484" + ], + "abnormal fecal osmolality": [ + "HP:0032485" + ], + "abnormal faecal osmolality": [ + "HP:0032485" + ], + "elevated fecal osmolality": [ + "HP:0032486" + ], + "elevated faecal osmolality": [ + "HP:0032486" + ], + "reduce fecal osmolality": [ + "HP:0032487" + ], + "reduced fecal osmolality": [ + "HP:0032487" + ], + "reduce faecal osmolality": [ + "HP:0032487" + ], + "reduced faecal osmolality": [ + "HP:0032487" + ], + "abnormal fecal ph": [ + "HP:0032488" + ], + "abnormal faecal ph": [ + "HP:0032488" + ], + "elevated fecal ph": [ + "HP:0032489" + ], + "elevated faecal ph": [ + "HP:0032489" + ], + "decreased fecal ph": [ + "HP:0032490" + ], + "decreased faecal ph": [ + "HP:0032490" + ], + "increase circulate argininosuccinic acid": [ + "HP:0032491" + ], + "increased circulating argininosuccinic acid": [ + "HP:0032491" + ], + "anti - myelin oligodendrocyte glycoprotein antibody positivity": [ + "HP:0032492" + ], + "anti - mog antibody positivity": [ + "HP:0032492" + ], + "increase circulating trypsinogen": [ + "HP:0032493" + ], + "increased circulating trypsinogen": [ + "HP:0032493" + ], + "increase immunoreactive trypsinogen": [ + "HP:0032493" + ], + "increased immunoreactive trypsinogen": [ + "HP:0032493" + ], + "abnormal terminal : vellus ratio": [ + "HP:0032495" + ], + "elevate terminal : vellus ratio": [ + "HP:0032496" + ], + "elevated terminal : vellus ratio": [ + "HP:0032496" + ], + "reduce terminal : vellus ratio": [ + "HP:0032497" + ], + "reduced terminal : vellus ratio": [ + "HP:0032497" + ], + "giant neutrophil granule": [ + "HP:0032499" + ], + "giant neutrophil granules": [ + "HP:0032499" + ], + "exacerbate by tobacco use": [ + "HP:0032500" + ], + "exacerbated by tobacco use": [ + "HP:0032500" + ], + "aggravate by tobacco use": [ + "HP:0032500" + ], + "aggravated by tobacco use": [ + "HP:0032500" + ], + "exacerbate by smoke": [ + "HP:0032500" + ], + "exacerbated by smoking": [ + "HP:0032500" + ], + "smoking or tobacco use exacerbate symptom": [ + "HP:0032500" + ], + "smoking or tobacco use exacerbates symptoms": [ + "HP:0032500" + ], + "exacerbate by contraceptive medication": [ + "HP:0032501" + ], + "exacerbated by contraceptive medication": [ + "HP:0032501" + ], + "contraceptive pill aggravate symptom": [ + "HP:0032501" + ], + "contraceptive pills aggravate symptoms": [ + "HP:0032501" + ], + "exacerbate by barbiturate medication": [ + "HP:0032502" + ], + "exacerbated by barbiturate medication": [ + "HP:0032502" + ], + "barbiturate produce worsen": [ + "HP:0032502" + ], + "barbiturates produce worsening": [ + "HP:0032502" + ], + "ameliorate by ethanol ingestion": [ + "HP:0032503" + ], + "ameliorated by ethanol ingestion": [ + "HP:0032503" + ], + "ethanol reduces manifestation": [ + "HP:0032503" + ], + "ethanol reduces manifestations": [ + "HP:0032503" + ], + "lhermitte 's sign": [ + "HP:0032504" + ], + "barber chair phenomenon": [ + "HP:0032504" + ], + "lhermitte 's phenomenon": [ + "HP:0032504" + ], + "hydrophobia": [ + "HP:0032505" + ], + "alien limb phenomenon": [ + "HP:0032506" + ], + "labiomental fasciculation": [ + "HP:0032507" + ], + "labiomental fasciculations": [ + "HP:0032507" + ], + "fasciculation , labiomental": [ + "HP:0032507" + ], + "fasciculations , labiomental": [ + "HP:0032507" + ], + "polyembolokoilamania": [ + "HP:0032508" + ], + "onychotillomania": [ + "HP:0032509" + ], + "tendon pain": [ + "HP:0032510" + ], + "superiorly position umbilicus": [ + "HP:0032511" + ], + "superiorly positioned umbilicus": [ + "HP:0032511" + ], + "four - vessel umbilical cord": [ + "HP:0032513" + ], + "duplicate lacrimal punctum": [ + "HP:0032514" + ], + "duplicated lacrimal punctum": [ + "HP:0032514" + ], + "double lacrimal puncta": [ + "HP:0032514" + ], + "lacrimal punctum , duplication": [ + "HP:0032514" + ], + "deep dermatophytosis": [ + "HP:0032515" + ], + "invasive dermatophyte infection": [ + "HP:0032516" + ], + "majocchi 's granuloma": [ + "HP:0032517" + ], + "disseminate dermatophytosis": [ + "HP:0032518" + ], + "disseminated dermatophytosis": [ + "HP:0032518" + ], + "increase burr cell count": [ + "HP:0032519" + ], + "increased burr cell count": [ + "HP:0032519" + ], + "masseter muscular weakness": [ + "HP:0032520" + ], + "self hugging": [ + "HP:0032521" + ], + "spasmodic upper - body squeeze": [ + "HP:0032521" + ], + "ameliorate by immunosuppresion": [ + "HP:0032522" + ], + "ameliorated by immunosuppresion": [ + "HP:0032522" + ], + "immunosupressive therapy improve condition": [ + "HP:0032522" + ], + "immunosupressive therapy improves condition": [ + "HP:0032522" + ], + "tendon thicken": [ + "HP:0032523" + ], + "tendon thickening": [ + "HP:0032523" + ], + "long thumb": [ + "HP:0032524" + ], + "aggravate by acetylcholinesterase inhibitor": [ + "HP:0032525" + ], + "aggravated by acetylcholinesterase inhibitor": [ + "HP:0032525" + ], + "ameliorate by acetylcholinesterase inhibitor": [ + "HP:0032526" + ], + "ameliorated by acetylcholinesterase inhibitor": [ + "HP:0032526" + ], + "inferiorly position umbilicus": [ + "HP:0032527" + ], + "inferiorly positioned umbilicus": [ + "HP:0032527" + ], + "low set umbilicus": [ + "HP:0032527" + ], + "low - set umbilicus": [ + "HP:0032527" + ], + "elevate urinary 4 - hydroxybutyric acid": [ + "HP:0032528" + ], + "elevated urinary 4 - hydroxybutyric acid": [ + "HP:0032528" + ], + "obsolete elevate circulate gamma - aminobutyric acid concentration": [ + "HP:0032529" + ], + "obsolete elevated circulating gamma - aminobutyric acid concentration": [ + "HP:0032529" + ], + "decrease succinic semialdehyde dehydrogenase level": [ + "HP:0032530" + ], + "decreased succinic semialdehyde dehydrogenase level": [ + "HP:0032530" + ], + "elevate csf gamma - aminobutyric acid concentration": [ + "HP:0032531" + ], + "elevated csf gamma - aminobutyric acid concentration": [ + "HP:0032531" + ], + "elevate csf 4 - hydroxybutyric acid concentration": [ + "HP:0032532" + ], + "elevated csf 4 - hydroxybutyric acid concentration": [ + "HP:0032532" + ], + "elevate csf gamma - hydroxybutyric acid": [ + "HP:0032532" + ], + "elevated csf gamma - hydroxybutyric acid": [ + "HP:0032532" + ], + "elevate csf ghb level": [ + "HP:0032532" + ], + "elevated csf ghb levels": [ + "HP:0032532" + ], + "elevate circulate acetone concentration": [ + "HP:0032533" + ], + "elevated circulating acetone concentration": [ + "HP:0032533" + ], + "exacerbate by methylxanthine ingestion": [ + "HP:0032534" + ], + "exacerbated by methylxanthine ingestion": [ + "HP:0032534" + ], + "methylxanthines produce worsen": [ + "HP:0032534" + ], + "methylxanthines produce worsening": [ + "HP:0032534" + ], + "cervical ( neck )": [ + "HP:0032535" + ], + "increased number of lymph node": [ + "HP:0032536" + ], + "increased number of lymph nodes": [ + "HP:0032536" + ], + "delay fracture heal": [ + "HP:0032537" + ], + "delayed fracture healing": [ + "HP:0032537" + ], + "pretibial dimple": [ + "HP:0032538" + ], + "joint extensor surface localization": [ + "HP:0032539" + ], + "joint flexor surface localization": [ + "HP:0032540" + ], + "knuckle pad": [ + "HP:0032541" + ], + "knuckle pad on dorsal aspect of finger joint": [ + "HP:0032541" + ], + "knuckle pads on dorsal aspect of finger joints": [ + "HP:0032541" + ], + "exacerbate by pregnancy": [ + "HP:0032542" + ], + "exacerbated by pregnancy": [ + "HP:0032542" + ], + "lithoptysis": [ + "HP:0032543" + ], + "predominant small joint localization": [ + "HP:0032544" + ], + "abdominal rigidity": [ + "HP:0032545" + ], + "rigid abdomen": [ + "HP:0032545" + ], + "abdominal guarding": [ + "HP:0032546" + ], + "low intraocular pressure": [ + "HP:0032547" + ], + "ocular hypotony": [ + "HP:0032547" + ], + "increase placental thickness": [ + "HP:0032548" + ], + "increased placental thickness": [ + "HP:0032548" + ], + "placental thickness increase": [ + "HP:0032548" + ], + "placental thickness increased": [ + "HP:0032548" + ], + "persistent asymmetrical tonic neck reflex": [ + "HP:0032549" + ], + "persistent fencer 's reflex": [ + "HP:0032549" + ], + "tonic neck reflex asymmetrical and persistent": [ + "HP:0032549" + ], + "howell - jolly body": [ + "HP:0032550" + ], + "howell - jolly bodies": [ + "HP:0032550" + ], + "hemorrhoid": [ + "HP:0032551" + ], + "hemorrhoids": [ + "HP:0032551" + ], + "haemorrhoid": [ + "HP:0032551" + ], + "haemorrhoids": [ + "HP:0032551" + ], + "pile": [ + "HP:0032551" + ], + "piles": [ + "HP:0032551" + ], + "abnormal pulse": [ + "HP:0032552" + ], + "weak pulse": [ + "HP:0032553" + ], + "absent pulse": [ + "HP:0032554" + ], + "bound pulse": [ + "HP:0032555" + ], + "bounding pulse": [ + "HP:0032555" + ], + "circumoral cyanosis": [ + "HP:0032556" + ], + "bluish around mouth": [ + "HP:0032556" + ], + "history of bone marrow transplant": [ + "HP:0032557" + ], + "status post haematopoietic stem cell transplantation": [ + "HP:0032557" + ], + "status post hematopoietic stem cell transplantation": [ + "HP:0032557" + ], + "absent sperm flagellum": [ + "HP:0032558" + ], + "absent sperm flagella": [ + "HP:0032558" + ], + "short sperm flagellum": [ + "HP:0032559" + ], + "short sperm flagella": [ + "HP:0032559" + ], + "coil sperm flagellum": [ + "HP:0032560" + ], + "coiled sperm flagella": [ + "HP:0032560" + ], + "microcephalic sperm head": [ + "HP:0032561" + ], + "small - head sperm": [ + "HP:0032561" + ], + "tapered sperm head": [ + "HP:0032562" + ], + "dacryocytosis": [ + "HP:0032563" + ], + "dacryocytes": [ + "HP:0032563" + ], + "tear - drop shape erythrocyte": [ + "HP:0032563" + ], + "tear - drop shaped erythrocytes": [ + "HP:0032563" + ], + "ileitis": [ + "HP:0032564" + ], + "inflammation of the ileum": [ + "HP:0032564" + ], + "vaginal mucosal ulceration": [ + "HP:0032565" + ], + "oval macrocytosis": [ + "HP:0032566" + ], + "lipiduria": [ + "HP:0032567" + ], + "urinary lipid excretion": [ + "HP:0032567" + ], + "urinary mulberry cell": [ + "HP:0032568" + ], + "urinary mulberry cells": [ + "HP:0032568" + ], + "temporal bossing": [ + "HP:0032569" + ], + "pontine ischemic lacunes": [ + "HP:0032570" + ], + "pontine ischaemic lacunes": [ + "HP:0032570" + ], + "increase oocyte death": [ + "HP:0032571" + ], + "increased oocyte death": [ + "HP:0032571" + ], + "abnormal urinary nucleobase concentration": [ + "HP:0032572" + ], + "elevate urinary cytidine": [ + "HP:0032573" + ], + "elevated urinary cytidine": [ + "HP:0032573" + ], + "elevate uridine in urine": [ + "HP:0032574" + ], + "elevated uridine in urine": [ + "HP:0032574" + ], + "decrease circulate 12 - hete": [ + "HP:0032575" + ], + "decreased circulating 12 - hete": [ + "HP:0032575" + ], + "decrease circulate 12 - hydroxyeicosatetraenoic acid concentration": [ + "HP:0032575" + ], + "decreased circulating 12 - hydroxyeicosatetraenoic acid concentration": [ + "HP:0032575" + ], + "intracellular accumulation of dol - pp - glcnac2man5": [ + "HP:0032576" + ], + "clonal t cell receptor rearrangement": [ + "HP:0032577" + ], + "third ventricle colloid cyst": [ + "HP:0032578" + ], + "vascular hamartoma": [ + "HP:0032579" + ], + "abnormal bulbus cordis morphology": [ + "HP:0032580" + ], + "abnormal renal insterstitial morphology": [ + "HP:0032581" + ], + "renal interstitial foam cell": [ + "HP:0032582" + ], + "renal interstitial foam cells": [ + "HP:0032582" + ], + "renal glomerular foam cell": [ + "HP:0032583" + ], + "renal glomerular foam cells": [ + "HP:0032583" + ], + "renal interstitial neutrophil infiltration": [ + "HP:0032584" + ], + "renal interstitial eosinophil infiltration": [ + "HP:0032585" + ], + "renal interstitial plasma cell infiltration": [ + "HP:0032586" + ], + "renal interstitial calcium oxalate": [ + "HP:0032587" + ], + "hand apraxia": [ + "HP:0032588" + ], + "lack of purposeful hand use": [ + "HP:0032588" + ], + "renal lymphocytic tubulitis": [ + "HP:0032589" + ], + "renal neutrophilic tubulitis": [ + "HP:0032590" + ], + "renal interstitial hemosiderin": [ + "HP:0032591" + ], + "aplasia of the right hemidiaphragm": [ + "HP:0032592" + ], + "right diaphragmatic hernia": [ + "HP:0032592" + ], + "myoglobin cast": [ + "HP:0032593" + ], + "myoglobin casts": [ + "HP:0032593" + ], + "renal tubular basement membrane denudation": [ + "HP:0032594" + ], + "denude tubular basement membrane": [ + "HP:0032594" + ], + "denuded tubular basement membrane": [ + "HP:0032594" + ], + "renal tubular epithelial cell detachment": [ + "HP:0032595" + ], + "renal tubular epithelial cell cytoplasmic vacuolization": [ + "HP:0032596" + ], + "renal tubular epithelial cell slough": [ + "HP:0032597" + ], + "renal tubular epithelial cell sloughing": [ + "HP:0032597" + ], + "blebbing of apical cytoplasm of renal tubular epithelial cell": [ + "HP:0032598" + ], + "blebbing of apical cytoplasm of renal tubular epithelial cells": [ + "HP:0032598" + ], + "abnormal renal tubular epithelial morphology": [ + "HP:0032599" + ], + "renal tubular epithelial cell hyaline droplet": [ + "HP:0032600" + ], + "renal tubular epithelial cell hyaline droplets": [ + "HP:0032600" + ], + "multinucleation of renal tubular epithelial cell": [ + "HP:0032601" + ], + "multinucleation of renal tubular epithelial cells": [ + "HP:0032601" + ], + "prominent nucleolus of renal tubular epithelial cell": [ + "HP:0032602" + ], + "prominent nucleoli of renal tubular epithelial cells": [ + "HP:0032602" + ], + "renal tubular epithelial cell simplification": [ + "HP:0032603" + ], + "renal tubular epithelial cell mitosis": [ + "HP:0032604" + ], + "high renal tubular epithelial cell n / c ratio": [ + "HP:0032605" + ], + "high n / c ratio of renal tubular epithelial cell": [ + "HP:0032605" + ], + "high n / c ratio of renal tubular epithelial cells": [ + "HP:0032605" + ], + "renal tubular epithelial lipofuscin": [ + "HP:0032606" + ], + "renal tubular epithelial cell swell": [ + "HP:0032607" + ], + "renal tubular epithelial cell swelling": [ + "HP:0032607" + ], + "thyroidization - type tubular atrophy": [ + "HP:0032608" + ], + "endocrine - type tubular atrophy": [ + "HP:0032609" + ], + "endocrinization pattern of tubular atrophy": [ + "HP:0032609" + ], + "renal tubular atrophy , endocrine - type": [ + "HP:0032609" + ], + "tubulointerstitial mycobacterial infiltration": [ + "HP:0032610" + ], + "renal tubulointerstitial mycobacterial organism": [ + "HP:0032610" + ], + "renal tubulointerstitial mycobacterial organisms": [ + "HP:0032610" + ], + "renal tubular epithelial cell hemosiderin": [ + "HP:0032611" + ], + "triphalangeal hallux": [ + "HP:0032612" + ], + "renal interstitial amyloid deposit": [ + "HP:0032613" + ], + "renal interstitial amyloid deposits": [ + "HP:0032613" + ], + "renal interstitial amyloid": [ + "HP:0032613" + ], + "renal interstitial amyloid deposition": [ + "HP:0032613" + ], + "renal interstitial amyloidosis": [ + "HP:0032613" + ], + "renal glomerular amyloid deposition": [ + "HP:0032614" + ], + "abnormal diffusion weight cerebral mri morphology": [ + "HP:0032615" + ], + "abnormal diffusion weighted cerebral mri morphology": [ + "HP:0032615" + ], + "diffusion weight imaging ( dwi ) abnormality": [ + "HP:0032615" + ], + "diffusion weighted imaging ( dwi ) abnormality": [ + "HP:0032615" + ], + "diffusion weight magnetic resonance imaging ( dwi ) abnormality": [ + "HP:0032615" + ], + "diffusion weighted magnetic resonance imaging ( dwi ) abnormality": [ + "HP:0032615" + ], + "mri diffusion abnormality of the cerebrum": [ + "HP:0032615" + ], + "renal interstitial immunoglobulin deposit": [ + "HP:0032616" + ], + "renal interstitial immunoglobulin deposits": [ + "HP:0032616" + ], + "renal interstitial immunoglobulin deposition": [ + "HP:0032616" + ], + "renal interstitial hemorrhage": [ + "HP:0032617" + ], + "renal interstitial haemorrhage": [ + "HP:0032617" + ], + "renal necrosis": [ + "HP:0032618" + ], + "renal parenchymal necrosis": [ + "HP:0032618" + ], + "perinephric abscess": [ + "HP:0032619" + ], + "intrarenal abscess": [ + "HP:0032620" + ], + "renal abscess": [ + "HP:0032620" + ], + "renal parenchymal abcess": [ + "HP:0032620" + ], + "hyperchromasia of renal tubular epithelial cell": [ + "HP:0032621" + ], + "hyperchromasia of renal tubular epithelial cells": [ + "HP:0032621" + ], + "condense chromatin of renal tubular epithelial cell": [ + "HP:0032621" + ], + "condensed chromatin of renal tubular epithelial cells": [ + "HP:0032621" + ], + "tubular luminal dilatation": [ + "HP:0032622" + ], + "renal intratubular cast": [ + "HP:0032623" + ], + "renal intratubular casts": [ + "HP:0032623" + ], + "tubular cast": [ + "HP:0032623" + ], + "tubular casts": [ + "HP:0032623" + ], + "intratubular bilirubin cast": [ + "HP:0032624" + ], + "intratubular bilirubin casts": [ + "HP:0032624" + ], + "intratubular erythrocyte cast": [ + "HP:0032625" + ], + "intratubular vancomycin cast": [ + "HP:0032626" + ], + "intratubular vancomycin casts": [ + "HP:0032626" + ], + "intratubular leukocyte cast": [ + "HP:0032627" + ], + "intratubular leukocyte casts": [ + "HP:0032627" + ], + "renal intratubular crystal": [ + "HP:0032628" + ], + "renal intratubular crystals": [ + "HP:0032628" + ], + "intratubular dihydroxyadenuria crystal": [ + "HP:0032629" + ], + "intratubular dihydroxyadenuria crystals": [ + "HP:0032629" + ], + "intratubular light - chain cast": [ + "HP:0032630" + ], + "intratubular light - chain casts": [ + "HP:0032630" + ], + "intratubular hemoglobin cast": [ + "HP:0032631" + ], + "intratubular hemoglobin casts": [ + "HP:0032631" + ], + "intratubular haemoglobin cast": [ + "HP:0032631" + ], + "intratubular haemoglobin casts": [ + "HP:0032631" + ], + "renal papillary necrosis": [ + "HP:0032632" + ], + "intratubular hyaline cast": [ + "HP:0032633" + ], + "intratubular hyaline casts": [ + "HP:0032633" + ], + "intratubular tamm - 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- convulsive status epilepticus with retained awareness": [ + "HP:0032869" + ], + "focal non - convulsive status epilepticus without impairment of awareness": [ + "HP:0032869" + ], + "focal impair awareness cognitive seizure with dyslexia / alexia": [ + "HP:0032870" + ], + "focal impaired awareness cognitive seizure with dyslexia / alexia": [ + "HP:0032870" + ], + "focal aware cognitive seizure with hallucination": [ + "HP:0032871" + ], + "focal impair awareness cognitive seizure with illusion": [ + "HP:0032872" + ], + "focal impaired awareness cognitive seizure with illusion": [ + "HP:0032872" + ], + "focal aware sensory seizure with cephalic sensation": [ + "HP:0032873" + ], + "focal impair awareness cognitive seizure with auditory agnosia": [ + "HP:0032874" + ], + "focal impaired awareness cognitive seizure with auditory agnosia": [ + "HP:0032874" + ], + "obsolete focal impaired awareness cognitive seizure with impaired responsiveness": [ + "HP:0032875" + ], + "focal aware cognitive 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sexual automatism seizure": [ + "HP:0032925" + ], + "focal impair awareness head nod automatism seizure": [ + "HP:0032926" + ], + "focal impaired awareness head nodding automatism seizure": [ + "HP:0032926" + ], + "focal impair awareness undressing automatism seizure": [ + "HP:0032927" + ], + "focal impaired awareness undressing automatism seizure": [ + "HP:0032927" + ], + "elevate csf neurofilamant light chain": [ + "HP:0032928" + ], + "elevated csf neurofilamant light chain": [ + "HP:0032928" + ], + "abnormal chondrocyte morphology": [ + "HP:0032929" + ], + "lacunar halo around chondrocytes": [ + "HP:0032930" + ], + "lacunar halos around chondrocytes": [ + "HP:0032930" + ], + "obsolete focal impaired awareness cognitive seizure with impaired attention": [ + "HP:0032931" + ], + "increase circulate pancreatic triacylglycerol lipase level": [ + "HP:0032932" + ], + "increased circulating pancreatic triacylglycerol lipase level": [ + "HP:0032932" + ], + "elevate circulate pancreatic 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"impaired ability to plan": [ + "HP:0033055" + ], + "ineffective planning": [ + "HP:0033055" + ], + "impaired ability to organize": [ + "HP:0033056" + ], + "impaired ability to organise": [ + "HP:0033056" + ], + "decrease serum terminal complement component": [ + "HP:0033057" + ], + "decreased serum terminal complement component": [ + "HP:0033057" + ], + "decrease serum complement c7": [ + "HP:0033058" + ], + "decreased serum complement c7": [ + "HP:0033058" + ], + "decrease serum complement c6": [ + "HP:0033059" + ], + "decreased serum complement c6": [ + "HP:0033059" + ], + "decrease serum complement c5": [ + "HP:0033060" + ], + "decreased serum complement c5": [ + "HP:0033060" + ], + "increase factor ix activity": [ + "HP:0033061" + ], + "increased factor ix activity": [ + "HP:0033061" + ], + "abnormal factor ix activity": [ + "HP:0033062" + ], + "shorten sleep cycle": [ + "HP:0033063" + ], + "shortened sleep cycle": [ + "HP:0033063" + ], + "short sleep": [ + "HP:0033063" + ], + 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level": [ + "HP:0033075" + ], + "inappropriately normal thyroid - stimulating hormone level": [ + "HP:0033075" + ], + "inappropriately normal tsh": [ + "HP:0033075" + ], + "abnormal circulate free t4 level": [ + "HP:0033076" + ], + "abnormal circulating free t4 level": [ + "HP:0033076" + ], + "abnormal circulate free thyroxine level": [ + "HP:0033076" + ], + "abnormal circulating free thyroxine level": [ + "HP:0033076" + ], + "increase circulate free t4 level": [ + "HP:0033077" + ], + "increased circulating free t4 level": [ + "HP:0033077" + ], + "decrease circulate free t4 level": [ + "HP:0033078" + ], + "decreased circulating free t4 level": [ + "HP:0033078" + ], + "aplasia / hypoplasia of the thyroid gland": [ + "HP:0033079" + ], + "abnormal tsh response to thyrotrophin - release hormone stimulation test": [ + "HP:0033080" + ], + "abnormal tsh response to thyrotrophin - releasing hormone stimulation test": [ + "HP:0033080" + ], + "abnormal tsh response to trh stimulation test": [ + 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urine": [ + "HP:0033088" + ], + "branch - chain aminoaciduria": [ + "HP:0033089" + ], + "branched - chain aminoaciduria": [ + "HP:0033089" + ], + "increase aromatic amino acid level in urine": [ + "HP:0033090" + ], + "increased aromatic amino acid level in urine": [ + "HP:0033090" + ], + "tyrosinuria": [ + "HP:0033091" + ], + "increase tyrosine in urine": [ + "HP:0033091" + ], + "increased tyrosine in urine": [ + "HP:0033091" + ], + "increase urine succinate level": [ + "HP:0033092" + ], + "increased urine succinate level": [ + "HP:0033092" + ], + "increase glutamine family amino acid level in urine": [ + "HP:0033093" + ], + "increased glutamine family amino acid level in urine": [ + "HP:0033093" + ], + "increase urine glutamate level": [ + "HP:0033094" + ], + "increased urine glutamate level": [ + "HP:0033094" + ], + "increase glutamic acid in urine": [ + "HP:0033094" + ], + "increased glutamic acid in urine": [ + "HP:0033094" + ], + "increase sulfur amino acid level in urine": [ + 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proteinogenic amino acid level": [ + "HP:0033098" + ], + "increase serine family amino acid in urine": [ + "HP:0033099" + ], + "increased serine family amino acid in urine": [ + "HP:0033099" + ], + "increase proteinogenic amino acid level in urine": [ + "HP:0033100" + ], + "increased proteinogenic amino acid level in urine": [ + "HP:0033100" + ], + "elevate urine aconitic acid level": [ + "HP:0033101" + ], + "elevated urine aconitic acid level": [ + "HP:0033101" + ], + "monkey wrench femoral neck": [ + "HP:0033102" + ], + "monkey wrench appearance of femoral neck": [ + "HP:0033102" + ], + "monkey wrench configuration of the proximal femur": [ + "HP:0033102" + ], + "swedish key appearance of femoral neck": [ + "HP:0033102" + ], + "swedish key configuration of the proximal femur": [ + "HP:0033102" + ], + "elevate circulate chi3l1 level": [ + "HP:0033103" + ], + "elevated circulating chi3l1 level": [ + "HP:0033103" + ], + "elevate circulate chitinase 3 - like 1 level": [ + "HP:0033103" + ], + "elevated circulating chitinase 3 - like 1 level": [ + "HP:0033103" + ], + "elevate circulate ykl40 level": [ + "HP:0033103" + ], + "elevated circulating ykl40 level": [ + "HP:0033103" + ], + "inappropriate absence of fever": [ + "HP:0033104" + ], + "interhypothalamic adhesion": [ + "HP:0033105" + ], + "hypothalamic adhesion": [ + "HP:0033105" + ], + "elevate circulate d - dimer concentration": [ + "HP:0033106" + ], + "elevated circulating d - dimer concentration": [ + "HP:0033106" + ], + "elevate d - dimer": [ + "HP:0033106" + ], + "elevated d - dimers": [ + "HP:0033106" + ], + "elevate fibrin degradation fragment concentration": [ + "HP:0033106" + ], + "elevated fibrin degradation fragment concentration": [ + "HP:0033106" + ], + "abnormal circulate proteinogenic amino acid concentration": [ + "HP:0033107" + ], + "abnormal circulating proteinogenic amino acid concentration": [ + "HP:0033107" + ], + "abnormal circulate proteinogenic amino acid derivative concentration": [ + 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medullary echogenicity": [ + "HP:0033131" + ], + "renal cortical hyperechogenicity": [ + "HP:0033132" + ], + "renal cortical hypoechogeneity": [ + "HP:0033133" + ], + "hypoechogenic renal cortex": [ + "HP:0033133" + ], + "abdominal adhesion": [ + "HP:0033134" + ], + "abdominal adhesions": [ + "HP:0033134" + ], + "intra - abdominal adhesion": [ + "HP:0033134" + ], + "hepatic infarction": [ + "HP:0033135" + ], + "lymph node abscess": [ + "HP:0033136" + ], + "abnormal pulmonary alveolar system morphology": [ + "HP:0033137" + ], + "right atrial thrombus": [ + "HP:0033138" + ], + "elevate circulate uracil concentration": [ + "HP:0033139" + ], + "elevated circulating uracil concentration": [ + "HP:0033139" + ], + "blake 's pouch cyst": [ + "HP:0033140" + ], + "severe sars - cov - 2 infection": [ + "HP:0033141" + ], + "long nasal bridge": [ + "HP:0033142" + ], + "jejunitis": [ + "HP:0033143" + ], + "abnormal circulate ceruloplasmin concentration": [ + "HP:0033144" + ], + "abnormal circulating ceruloplasmin concentration": [ + "HP:0033144" + ], + "increase circulate ceruloplasmin concentration": [ + "HP:0033145" + ], + "increased circulating ceruloplasmin concentration": [ + "HP:0033145" + ], + "elevate circulate methylsuccinic acid concentration": [ + "HP:0033146" + ], + "elevated circulating methylsuccinic acid concentration": [ + "HP:0033146" + ], + "abnormal circulate short - chain fatty - acid concentration": [ + "HP:0033147" + ], + "abnormal circulating short - chain fatty - acid concentration": [ + "HP:0033147" + ], + "increase circulate isovaleric acid concentration": [ + "HP:0033148" + ], + "increased circulating isovaleric acid concentration": [ + "HP:0033148" + ], + "increase circulating isovalerate": [ + "HP:0033148" + ], + "increased circulating isovalerate": [ + "HP:0033148" + ], + "isovalericacidemia": [ + "HP:0033148" + ], + "intrahepatic bile duct dilatation": [ + "HP:0033149" + ], + "dilatation of intrahepatic biliary duct": [ + "HP:0033149" + ], + 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circulate 3 - methylhistidine concentration": [ + "HP:0033157" + ], + "elevated circulating 3 - methylhistidine concentration": [ + "HP:0033157" + ], + "reduce respiratory ciliary beating frequency": [ + "HP:0033158" + ], + "reduced respiratory ciliary beating frequency": [ + "HP:0033158" + ], + "dminished respiratory ciliary beat frequency": [ + "HP:0033158" + ], + "reduce urinary inosine level": [ + "HP:0033159" + ], + "reduced urinary inosine level": [ + "HP:0033159" + ], + "decrease urinary guanosine level": [ + "HP:0033160" + ], + "decreased urinary guanosine level": [ + "HP:0033160" + ], + "abnormal urinary purine level": [ + "HP:0033161" + ], + "abnormal urinary pyrimidine level": [ + "HP:0033162" + ], + "small intestinal bacterial overgrowth": [ + "HP:0033163" + ], + "focal active colitis": [ + "HP:0033164" + ], + "necrotizing enterocolitis": [ + "HP:0033165" + ], + "recurrent viral upper respiratory tract infection": [ + "HP:0033166" + ], + "recurrent viral upper respiratory tract infections": [ + "HP:0033166" + ], + "neutrophilic urticarial dermatosis": [ + "HP:0033167" + ], + "reduce mevalonate kinase activity": [ + "HP:0033168" + ], + "reduced mevalonate kinase activity": [ + "HP:0033168" + ], + "reduce total lung capacity": [ + "HP:0033169" + ], + "reduced total lung capacity": [ + "HP:0033169" + ], + "reduce tlc": [ + "HP:0033169" + ], + "reduced tlc": [ + "HP:0033169" + ], + "abnormal skinfold thickness measurement": [ + "HP:0033170" + ], + "abnormal triceps skinfold thickness": [ + "HP:0033171" + ], + "increase triceps skinfold thickness": [ + "HP:0033172" + ], + "increased triceps skinfold thickness": [ + "HP:0033172" + ], + "milky appearance of bronchoalveolar lavage fluid": [ + "HP:0033173" + ], + "bloody bronchoalveolar lavage fluid": [ + "HP:0033174" + ], + "elevate circulate 5 - oxoproline concentration": [ + "HP:0033175" + ], + "elevated circulating 5 - oxoproline concentration": [ + "HP:0033175" + ], + "elevate circulate l - pyroglutamic acid concentration": [ + "HP:0033175" + ], + "elevated circulating l - pyroglutamic acid concentration": [ + "HP:0033175" + ], + "submandibular lymph node enlargement": [ + "HP:0033176" + ], + "submandibular lymphadenopathy": [ + "HP:0033176" + ], + "elevate circulate suberic acid concentration": [ + "HP:0033177" + ], + "elevated circulating suberic acid concentration": [ + "HP:0033177" + ], + "increase circulate interleukin 8": [ + "HP:0033178" + ], + "increased circulating interleukin 8": [ + "HP:0033178" + ], + "increase serum il - 8": [ + "HP:0033178" + ], + "increased serum il - 8": [ + "HP:0033178" + ], + "increase serum interleukin 8": [ + "HP:0033178" + ], + "increased serum interleukin 8": [ + "HP:0033178" + ], + "increase serum interleukin - 8": [ + "HP:0033178" + ], + "increased serum interleukin - 8": [ + "HP:0033178" + ], + "elevate circulate aconitic acid concentration": [ + "HP:0033179" + ], + "elevated circulating aconitic acid concentration": [ + "HP:0033179" + ], + 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], + "perioral erythema": [ + "HP:0033194" + ], + "perianal erythema": [ + "HP:0033195" + ], + "portal inflammation": [ + "HP:0033196" + ], + "hepatic portal inflammation": [ + "HP:0033196" + ], + "hepatic lobular inflammation": [ + "HP:0033197" + ], + "trigger by viral infection": [ + "HP:0033198" + ], + "triggered by viral infection": [ + "HP:0033198" + ], + "increase circulate interleukin 10": [ + "HP:0033199" + ], + "increased circulating interleukin 10": [ + "HP:0033199" + ], + "increase serum interleukin 10": [ + "HP:0033199" + ], + "increased serum interleukin 10": [ + "HP:0033199" + ], + "triceps hyporeflexia": [ + "HP:0033200" + ], + "hyporeflexia of triceps": [ + "HP:0033200" + ], + "biceps hyporeflexia": [ + "HP:0033201" + ], + "hyporeflexia of biceps": [ + "HP:0033201" + ], + "brachioradialis hyporeflexia": [ + "HP:0033202" + ], + "brachioradialis hyperreflexia": [ + "HP:0033203" + ], + "triceps hyperreflexia": [ + "HP:0033204" + ], + "biceps hyperreflexia": [ + "HP:0033205" + ], + "hyperactive achilles reflex": [ + "HP:0033206" + ], + "hyperactive ankle jerk reflex": [ + "HP:0033206" + ], + "hyperactive ankle reflex": [ + "HP:0033206" + ], + "increase proportion autoreactive unresponsive cd21 - / low b cell": [ + "HP:0033207" + ], + "increased proportion autoreactive unresponsive cd21 - / low b cells": [ + "HP:0033207" + ], + "alveolar capillary dysplasia": [ + "HP:0033208" + ], + "acinar dysplasia": [ + "HP:0033209" + ], + "congenital alveolar dysplasia": [ + "HP:0033210" + ], + "decrease total iron binding capacity": [ + "HP:0033211" + ], + "decreased total iron binding capacity": [ + "HP:0033211" + ], + "abnormal total iron binding capacity": [ + "HP:0033212" + ], + "elevate urine suberic acid level": [ + "HP:0033213" + ], + "elevated urine suberic acid level": [ + "HP:0033213" + ], + "elevate urine octanedioic acid level": [ + "HP:0033213" + ], + "elevated urine octanedioic acid level": [ + "HP:0033213" + ], + "recurrent viral pneumonia": [ + "HP:0033214" + ], + "obliterative abnormality of the renal glomerulus": [ + "HP:0033215" + ], + "glomerular hyalinosis": [ + "HP:0033216" + ], + "perihilar glomerular hyalinosis": [ + "HP:0033217" + ], + "glomerular hyalinosis at the tubular pole": [ + "HP:0033218" + ], + "glomerular hyalinosis away from the vascular and tubular pole": [ + "HP:0033219" + ], + "glomerular hyalinosis away from the vascular and tubular poles": [ + "HP:0033219" + ], + "2 - ethylhydracylic aciduria": [ + "HP:0033220" + ], + "elevate urinary 2 - ethylhydracylic acid": [ + "HP:0033220" + ], + "elevated urinary 2 - ethylhydracylic acid": [ + "HP:0033220" + ], + "elevate urinary 2 - methylbutyrylglycine": [ + "HP:0033220" + ], + "elevated urinary 2 - methylbutyrylglycine": [ + "HP:0033220" + ], + "increase cd4 : cd8 ratio": [ + "HP:0033221" + ], + "increased cd4 : cd8 ratio": [ + "HP:0033221" + ], + "decrease cd4 : cd8 ratio": [ + "HP:0033222" + ], + "decreased cd4 : cd8 ratio": [ + "HP:0033222" + ], + "invert cd4 / cd8 ratio": [ + "HP:0033222" + ], + "inverted cd4 / cd8 ratio": [ + "HP:0033222" + ], + "invert cd4 : cd8 ratio": [ + "HP:0033222" + ], + "inverted cd4 : cd8 ratio": [ + "HP:0033222" + ], + "abnormal glomerular parietal epithelial cell morphology": [ + "HP:0033223" + ], + "glomerular parietal epithelial cell hyperplasia": [ + "HP:0033224" + ], + "hyperplasia of the glomerular parietal epithelial cell": [ + "HP:0033224" + ], + "glomerular parietal epithelial cell hypertrophy": [ + "HP:0033225" + ], + "hypertrophy of the glomerular parietal epithelial cell": [ + "HP:0033225" + ], + "bowman capsular hyaline drop": [ + "HP:0033226" + ], + "bowman capsular hyaline drops": [ + "HP:0033226" + ], + "capsular hyaline drop within bowman 's capsule": [ + "HP:0033226" + ], + "capsular hyaline drops within bowman 's capsule": [ + "HP:0033226" + ], + "glomerular synechial adhesion": [ + "HP:0033227" + ], + "triceps areflexia": [ + "HP:0033228" + ], + "areflexia of triceps": [ + "HP:0033228" + ], + "brachioradialis areflexia": [ + "HP:0033229" + ], + "areflexia of brachioradialis": [ + "HP:0033229" + ], + "biceps areflexia": [ + "HP:0033230" + ], + "areflexia of biceps": [ + "HP:0033230" + ], + "abnormal glomerular mesangial cellularity": [ + "HP:0033231" + ], + "abnormal glomerular mesangial matrix morphology": [ + "HP:0033232" + ], + "paramesangial deposit": [ + "HP:0033233" + ], + "paramesangial deposits": [ + "HP:0033233" + ], + "mesangial hyaline deposition": [ + "HP:0033234" + ], + "difficulty descend stair": [ + "HP:0033235" + ], + "difficulty descending stairs": [ + "HP:0033235" + ], + "difficulty walk down stair": [ + "HP:0033235" + ], + "difficulty walking down stairs": [ + "HP:0033235" + ], + "cognitive fatigue": [ + "HP:0033236" + ], + "central fatigue": [ + "HP:0033236" + ], + "visceral epithelial cell detachment": [ + "HP:0033237" + ], + "detachment of visceral epithelial cell": [ + "HP:0033237" + ], + "detachment of visceral epithelial cells": [ 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ii cell morphology": [ + "HP:0033245" + ], + "abnormal type ii pneumocyte morphology": [ + "HP:0033245" + ], + "type ii pneumocyte hypertrophy": [ + "HP:0033246" + ], + "hypertrophic alveolar type ii cell": [ + "HP:0033246" + ], + "hypertrophic alveolar type ii cells": [ + "HP:0033246" + ], + "hypertrophic alveolar type ii pneumocytes": [ + "HP:0033246" + ], + "pulmonary amyloidosis": [ + "HP:0033247" + ], + "multiple pulmonary interstitial hyalinized nodule": [ + "HP:0033248" + ], + "multiple pulmonary interstitial hyalinized nodules": [ + "HP:0033248" + ], + "focal substantia nigra t2 hyperintensity": [ + "HP:0033249" + ], + "focal substantia nigra t2 hyperintense lesion": [ + "HP:0033249" + ], + "nailfold capillary tortuosity": [ + "HP:0033250" + ], + "elevate residual volume": [ + "HP:0033251" + ], + "elevated residual volume": [ + "HP:0033251" + ], + "elevate rv": [ + "HP:0033251" + ], + "elevated rv": [ + "HP:0033251" + ], + "palmar hyperlinearity": [ + "HP:0033252" + ], + "reduce circulate interferon gamma": [ + "HP:0033253" + ], + "reduced circulating interferon gamma": [ + "HP:0033253" + ], + "anorectal stricture": [ + "HP:0033254" + ], + "stricture of the anorectum": [ + "HP:0033254" + ], + "congenital lobar overinflation": [ + "HP:0033255" + ], + "congenital lobar emphysema": [ + "HP:0033255" + ], + "pancolitis": [ + "HP:0033256" + ], + "delay ability to walk with support": [ + "HP:0033257" + ], + "delayed ability to walk with support": [ + "HP:0033257" + ], + "delay ability to cruise": [ + "HP:0033257" + ], + "delayed ability to cruise": [ + "HP:0033257" + ], + "sudden unexpected death in epilepsy": [ + "HP:0033258" + ], + "non - motor seizure": [ + "HP:0033259" + ], + "livedo racemosa": [ + "HP:0033260" + ], + "renal artery aneurysm": [ + "HP:0033261" + ], + "transphyseal fracture of the distal humerus": [ + "HP:0033262" + ], + "transphyseal distal humerus fracture": [ + "HP:0033262" + ], + "absent platelet dense granule": [ + "HP:0033263" + ], + "absent platelet dense granules": [ + "HP:0033263" + ], + "absent platelet dense body": [ + "HP:0033263" + ], + "absent platelet dense bodies": [ + "HP:0033263" + ], + "enlarge platelet dense granule": [ + "HP:0033264" + ], + "enlarged platelet dense granules": [ + "HP:0033264" + ], + "podocyte myelin figure": [ + "HP:0033265" + ], + "podocyte myelin figures": [ + "HP:0033265" + ], + "podocyte myelin inclusion": [ + "HP:0033265" + ], + "podocyte myelin inclusions": [ + "HP:0033265" + ], + "glomerular pseudocrescent": [ + "HP:0033266" + ], + "abnormal glomerular capillary lumen morphology": [ + "HP:0033267" + ], + "deflation of the glomerular tuft": [ + "HP:0033268" + ], + "glomerular capillary collapse": [ + "HP:0033269" + ], + "collapse of glomerular capillary wall": [ + "HP:0033269" + ], + "collapse of glomerular capillary walls": [ + "HP:0033269" + ], + "glomerular capillary congestion": [ + "HP:0033270" + ], + "glomerular congestion": [ + "HP:0033270" + ], + "glomerular capillary microaneurysm": [ + "HP:0033271" + ], + "abnormal glomerular endothelial cell morphology": [ + "HP:0033272" + ], + "loss of glomerular endothelial cell fenestration": [ + "HP:0033273" + ], + "glomerular endotheliosis": [ + "HP:0033274" + ], + "glomerular endothelial tubuloreticular inclusion": [ + "HP:0033275" + ], + "obsolete glomerular endocapillary hypercellularity": [ + "HP:0033276" + ], + "glomerular fibrinoid necrosis": [ + "HP:0033277" + ], + "reduce cd95 - induced lymphocyte apoptosis": [ + "HP:0033278" + ], + "reduced cd95 - induced lymphocyte apoptosis": [ + "HP:0033278" + ], + "enterocutaneous fistula": [ + "HP:0033279" + ], + "paratracheal lymphadenopathy": [ + "HP:0033280" + ], + "circulate nucleate red blood cell": [ + "HP:0033281" + ], + "circulating nucleated red blood cells": [ + "HP:0033281" + ], + "abnormal glomerular basement membrane morphology": [ + "HP:0033282" + ], + "segmentally thicken glomerular basement membrane": [ + "HP:0033283" + ], + "segmentally thickened glomerular basement membrane": [ + "HP:0033283" + ], + "diffusely thicken glomerular basement membrane": [ + "HP:0033284" + ], + "diffusely thickened glomerular basement membrane": [ + "HP:0033284" + ], + "thicken glomerular basement membrane with no electron dense deposit": [ + "HP:0033285" + ], + "thickened glomerular basement membranes with no electron dense deposits": [ + "HP:0033285" + ], + "thicken glomerular basement membrane with electron dense deposit": [ + "HP:0033286" + ], + "thickened glomerular basement membranes with electron dense deposits": [ + "HP:0033286" + ], + "glomerular basement membrane lucencies": [ + "HP:0033287" + ], + "glomerular basement membrane spike": [ + "HP:0033288" + ], + "glomerular basement membrane spikes": [ + "HP:0033288" + ], + "glomerular basement membrane wrinkle": [ + "HP:0033289" + ], + "glomerular basement membrane wrinkling": [ + "HP:0033289" + ], + "glomerular subendothelial widening": [ + "HP:0033290" + ], + "glomerular karyhorrhectic debris": [ + "HP:0033291" + ], + "glomerular fibrin thrombus": [ + "HP:0033292" + ], + "glomerular hyaline pseudothrombus": [ + "HP:0033293" + ], + "glomerular lipoprotein thrombus": [ + "HP:0033294" + ], + "mesangial immune complex deposition": [ + "HP:0033295" + ], + "binucleated visceral epithelial cell": [ + "HP:0033296" + ], + "binucleated visceral epithelial cells": [ + "HP:0033296" + ], + "binucleated podocytes": [ + "HP:0033296" + ], + "multinucleated visceral epithelial cell": [ + "HP:0033297" + ], + "multinucleated visceral epithelial cells": [ + "HP:0033297" + ], + "multinucleated podocytes": [ + "HP:0033297" + ], + "podocyte multinucleation": [ + "HP:0033297" + ], + "abnormal circulate complement factor h related protein 1 concentration": [ + "HP:0033298" + ], + "abnormal circulating complement factor h related protein 1 concentration": [ + "HP:0033298" + ], + "reduce circulate complement factor h related protein 1 concentration": [ + "HP:0033299" + ], + "reduced circulating complement factor h related protein 1 concentration": [ + "HP:0033299" + ], + "increase circulate complement factor h related protein 1 concentration": [ + "HP:0033300" + ], + "increased circulating complement factor h related protein 1 concentration": [ + "HP:0033300" + ], + "elevate circulate 1 - methylhistidine concentration": [ + "HP:0033301" + ], + "elevated circulating 1 - methylhistidine concentration": [ + "HP:0033301" + ], + "elevate circulate 4 - hydroxyphenylacetic acid concentration": [ + "HP:0033302" + ], + "elevated circulating 4 - hydroxyphenylacetic acid concentration": [ + "HP:0033302" + ], + "elevate urinary monocarboxylic acid level": [ + "HP:0033303" + ], + "elevated urinary monocarboxylic acid level": [ + "HP:0033303" + ], + "elevate urine 4 - hydroxyphenylacetic acid level": [ + "HP:0033304" + ], + "elevated urine 4 - hydroxyphenylacetic acid level": [ + "HP:0033304" + ], + "abnormal circulate fetuin a concentration": [ + "HP:0033305" + ], + "abnormal circulating fetuin a concentration": [ + "HP:0033305" + ], + "decrease circulate fetuin a concentration": [ + "HP:0033306" + ], + "decreased circulating fetuin a concentration": [ + "HP:0033306" + ], + "increase circulate fetuin a concentration": [ + "HP:0033307" + ], + "increased circulating fetuin a concentration": [ + "HP:0033307" + ], + "patellar overgrowth": [ + "HP:0033308" + ], + "ileoileal intussusception": [ + "HP:0033309" + ], + "osmotic diarrhea": [ + "HP:0033310" + ], + "abdominal aortic dissection": [ + "HP:0033311" + ], + "abnormal bowman space morphology": [ + "HP:0033312" + ], + "urinary space collagenization": [ + "HP:0033313" + ], + "collagenization of the urinary space": [ + "HP:0033313" + ], + "visceral epithelial cell hyperplasia": [ + "HP:0033314" + ], + "hyperplasia of visceral epithelial cell": [ + "HP:0033314" + ], + "hyperplasia of visceral epithelial cells": [ + "HP:0033314" + ], + "podocyte hyperplasia": [ + "HP:0033314" + ], + "visceral epithelial hyaline droplet": [ + "HP:0033315" + ], + "visceral epithelial hyaline droplets": [ + "HP:0033315" + ], + "glomerular crescent formation": [ + "HP:0033316" + ], + "cellular crescent": [ + "HP:0033317" + ], + "fibrocellular crescent": [ + "HP:0033318" + ], + "fibrous crescent": [ + "HP:0033319" + ], + "mesangial cell loss": [ + "HP:0033320" + ], + "glomerular obsolescence": [ + "HP:0033321" + ], + "glomerular capillary wall duplication without cellular interposition": [ + "HP:0033322" + ], + "glomerular capillary wall duplication with cellular interposition": [ + "HP:0033323" + ], + "elevate circulate homovanillic acid concentration": [ + "HP:0033324" + ], + "elevated circulating homovanillic acid concentration": [ + "HP:0033324" + ], + "elevate circulate sebacic acid concentration": [ + "HP:0033325" + ], + "elevated circulating sebacic acid concentration": [ + "HP:0033325" + ], + "elevate circulate hydroxyphenlyllactic acid concentration": [ + "HP:0033326" + ], + "elevated circulating hydroxyphenlyllactic acid concentration": [ + "HP:0033326" + ], + "nail psoriasis": [ + "HP:0033327" + ], + "type ii pneumocyte hyperplasia": [ + "HP:0033328" + ], + "abnormal postural reflex": [ + "HP:0033329" + ], + "abnormal postural reaction": [ + "HP:0033329" + ], + "impaired neck - righting reflex": [ + "HP:0033330" + ], + "acute phase response": [ + "HP:0033331" + ], + "elevate circulate amyloid a": [ + "HP:0033332" + ], + "elevated circulating amyloid a": [ + "HP:0033332" + ], + "jaw contracture": [ + "HP:0033333" + ], + "abnormal embryonic development": [ + "HP:0033334" + ], + "abnormal preimplantation embryonic development": [ + "HP:0033335" + ], + "zygotic cleavage failure": [ + "HP:0033336" + ], + "failure of zygotic cell division": [ + "HP:0033336" + ], + "abnormal gametogenesis": [ + "HP:0033337" + ], + "abnormal female meiosis": [ + "HP:0033338" + ], + "increase circulate inosine concentration": [ + "HP:0033339" + ], + "increased circulating inosine concentration": [ + "HP:0033339" + ], + "increase circulate guanosine concentration": [ + "HP:0033340" + ], + "increased circulating guanosine concentration": [ + "HP:0033340" + ], + "elevate circulate sitosterol concentration": [ + "HP:0033341" + ], + "elevated circulating sitosterol concentration": [ + "HP:0033341" + ], + "elevate circulate beta - sitosterol concentration": [ + "HP:0033341" + ], + "elevated circulating beta - sitosterol concentration": [ + "HP:0033341" + ], + "anti - aquaporin 4 antibody positivity": [ + "HP:0033342" + ], + "anti - aqp4 antibody positivity": [ + "HP:0033342" + ], + "mucoid diarrhea": [ + "HP:0033343" + ], + "mucous diarrhea": [ + "HP:0033343" + ], + "mucous diarrhoea": [ + "HP:0033343" + ], + "pleural cobblestoning": [ + "HP:0033344" + ], + "neuralgia": [ + "HP:0033345" + ], + "psychic epileptic aura": [ + "HP:0033346" + ], + "psychic aura": [ + "HP:0033346" + ], + "cognitive epileptic aura": [ + "HP:0033347" + ], + "epileptic aura": [ + "HP:0033348" + ], + "seizure cluster": [ + "HP:0033349" + ], + "acute repetitive seizure": [ + "HP:0033349" + ], + "acute repetitive seizures": [ + "HP:0033349" + ], + "crescendo seizure": [ + "HP:0033349" + ], + "crescendo seizures": [ + "HP:0033349" + ], + "cyclical seizure": [ + "HP:0033349" + ], + "cyclical seizures": [ + "HP:0033349" + ], + "recurrent seizure": [ + "HP:0033349" + ], + "recurrent seizures": [ + "HP:0033349" + ], + "seizure flurry": [ + "HP:0033349" + ], + "seizure flurries": [ + "HP:0033349" + ], + "serial seizure": [ + "HP:0033349" + ], + "serial seizures": [ + "HP:0033349" + ], + "elevate forced expiratory volume in one second": [ + "HP:0033350" + ], + "elevated forced expiratory volume in one second": [ + "HP:0033350" + ], + "elevate fev1": [ + "HP:0033350" + ], + "elevated fev1": [ + "HP:0033350" + ], + "candida esophagitis": [ + "HP:0033351" + ], + "esophageal candidiasis": [ + "HP:0033351" + ], + "pulmonary hypertensive crisis": [ + "HP:0033352" + ], + "pulmonary arterial hypertension 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membrane": [ + "HP:0033363" + ], + "hyaline membranes": [ + "HP:0033363" + ], + "lipoid pneumonia": [ + "HP:0033364" + ], + "endogenous lipoid pneumonia": [ + "HP:0033365" + ], + "exogenous lipoid pneumonia": [ + "HP:0033366" + ], + "orthodeoxia": [ + "HP:0033367" + ], + "platypnea": [ + "HP:0033368" + ], + "cavitating leukodystrophy": [ + "HP:0033369" + ], + "bronchial telangiectasia": [ + "HP:0033370" + ], + "endobronchial telangiectasia": [ + "HP:0033370" + ], + "bronchocentric granulomatosis": [ + "HP:0033371" + ], + "abnormal kco": [ + "HP:0033372" + ], + "increase kco": [ + "HP:0033373" + ], + "increased kco": [ + "HP:0033373" + ], + "decrease kco": [ + "HP:0033374" + ], + "decreased kco": [ + "HP:0033374" + ], + "anthracosis": [ + "HP:0033375" + ], + "alveolar septal thickening": [ + "HP:0033376" + ], + "increase airway neuroendocrine cell": [ + "HP:0033377" + ], + "increased airway neuroendocrine cells": [ + "HP:0033377" + ], + "increase airway neuroepithelial body": [ + "HP:0033378" + ], + "increased airway neuroepithelial bodies": [ + "HP:0033378" + ], + "bilateral superior vena cava": [ + "HP:0033379" + ], + "bilateral svc": [ + "HP:0033379" + ], + "nasal chondritis": [ + "HP:0033380" + ], + "nose chondritis": [ + "HP:0033380" + ], + "elevate circulate stearoylcarnitine concentration": [ + "HP:0033381" + ], + "elevated circulating stearoylcarnitine concentration": [ + "HP:0033381" + ], + "elevate circulate palmitoylcarnitine concentration": [ + "HP:0033382" + ], + "elevated circulating palmitoylcarnitine concentration": [ + "HP:0033382" + ], + "decrease compound muscle action potential amplitude": [ + "HP:0033383" + ], + "decreased compound muscle action potential amplitude": [ + "HP:0033383" + ], + "decrease cmap amplitude": [ + "HP:0033383" + ], + "decreased cmap amplitude": [ + "HP:0033383" + ], + "elevate urinary collagen degradation product": [ + "HP:0033384" + ], + "elevated urinary collagen degradation products": [ + "HP:0033384" + ], + "elevate urine pyridinoline level": [ + "HP:0033385" + ], + "elevated urine pyridinoline level": [ + "HP:0033385" + ], + "elevate urine hydroxylysyl - pyridinoline level": [ + "HP:0033385" + ], + "elevated urine hydroxylysyl - pyridinoline level": [ + "HP:0033385" + ], + "abnormal circulate collagen degradation product concentration": [ + "HP:0033386" + ], + "abnormal circulating collagen degradation product concentration": [ + "HP:0033386" + ], + "elevate circulate pyridinoline concentration": [ + "HP:0033387" + ], + "elevated circulating pyridinoline concentration": [ + "HP:0033387" + ], + "abnormal bronchial artery morphology": [ + "HP:0033388" + ], + "bronchopulmonary anastomosis": [ + "HP:0033389" + ], + "bronchial artery dilatation": [ + "HP:0033390" + ], + "bronchial artery enlargement": [ + "HP:0033390" + ], + "dilatation of a bronchial artery": [ + "HP:0033390" + ], + "bronchial artery hypertrophy": [ + "HP:0033391" + ], + "perivascular pre - capillary pulmonary artery inflammation": [ + "HP:0033392" + ], + "perivascular inflammation of arteriole in the pulmonary circulation": [ + "HP:0033392" + ], + "perivascular inflammation of arterioles in the pulmonary circulation": [ + "HP:0033392" + ], + "perivascular inflammation of pre - capillary pulmonary artery": [ + "HP:0033392" + ], + "perivascular inflammation of pre - capillary pulmonary arteries": [ + "HP:0033392" + ], + "irregularly shaped sperm tail": [ + "HP:0033393" + ], + "sperm flagellum with irregular caliber": [ + "HP:0033393" + ], + "sperm flagella with irregular caliber": [ + "HP:0033393" + ], + "sperm flagellum with irregular calibre": [ + "HP:0033393" + ], + "sperm flagella with irregular calibre": [ + "HP:0033393" + ], + "anti - carbonic anhydrase ii antibody positivity": [ + "HP:0033394" + ], + "antilactoferrin antibody positivity": [ + "HP:0033395" + ], + "glomerular extracapillary fibrin": [ + "HP:0033396" + ], + "bowman - space proteinaceous debris": [ + "HP:0033397" + ], + "pleural plaque": [ + "HP:0033398" + ], + "persistent fever": [ + "HP:0033399" + ], + "acute abdomen": [ + "HP:0033400" + ], + "acute abdominal pain": [ + "HP:0033400" + ], + "tissue ischemia": [ + "HP:0033401" + ], + "digital ischemia": [ + "HP:0033402" + ], + "testicular ischemia": [ + "HP:0033403" + ], + "intestinal ischemia": [ + "HP:0033404" + ], + "abnormal circulate organic amino compound concentration": [ + "HP:0033405" + ], + "abnormal circulating organic amino compound concentration": [ + "HP:0033405" + ], + "elevate circulate o - phosphoethanolamine concentration": [ + "HP:0033406" + ], + "elevated circulating o - phosphoethanolamine concentration": [ + "HP:0033406" + ], + "elevate urine acetoacetic acid level": [ + "HP:0033407" + ], + "elevated urine acetoacetic acid level": [ + "HP:0033407" + ], + "elevate circulate acetoacetic acid concentration": [ + "HP:0033408" + ], + "elevated circulating acetoacetic acid concentration": [ + "HP:0033408" + ], + "elevate urinary 2 - hydroxybutyric acid": [ + "HP:0033409" + ], + "elevated urinary 2 - hydroxybutyric acid": [ + "HP:0033409" + ], + "elevate circulating cartilage oligomeric matrix protein concentration": [ + "HP:0033410" + ], + "elevated circulating cartilage oligomeric matrix protein concentration": [ + "HP:0033410" + ], + "low extremity akinesia": [ + "HP:0033411" + ], + "lower extremity akinesia": [ + "HP:0033411" + ], + "upper extremity akinesia": [ + "HP:0033412" + ], + "akinesia of the upper extremity": [ + "HP:0033412" + ], + "akinesia of the upper extremities": [ + "HP:0033412" + ], + "upper extremity hypokinesia": [ + "HP:0033413" + ], + "hypokinesia of the upper extremity": [ + "HP:0033413" + ], + "hypokinesia of the upper extremities": [ + "HP:0033413" + ], + "low extremity hypokinesia": [ + "HP:0033414" + ], + "lower extremity hypokinesia": [ + "HP:0033414" + ], + "hypokinesia of the low extremity": [ + "HP:0033414" + ], + "hypokinesia of the lower extremities": [ + "HP:0033414" + ], + "cardiac tamponade": [ + "HP:0033415" + ], + "hip adductor weakness": [ + "HP:0033416" + ], + "elevate circulate hydroxybutyric acid concentration": [ + "HP:0033417" + ], + "elevated circulating hydroxybutyric acid concentration": [ + "HP:0033417" + ], + "elevate circulate 2 - hydroxybutyric acid concentration": [ + "HP:0033418" + ], + "elevated circulating 2 - hydroxybutyric acid concentration": [ + "HP:0033418" + ], + "elevate circulate 3 - hydroxybutyric acid concentration": [ + "HP:0033419" + ], + "elevated circulating 3 - hydroxybutyric acid concentration": [ + "HP:0033419" + ], + "pulmonary arterial plexiform lesion": [ + "HP:0033420" + ], + "pulmonary artery intimal thicken": [ + "HP:0033421" + ], + "pulmonary artery intimal thickening": [ + "HP:0033421" + ], + "pulmonary artery adventitial fibrosis": [ + "HP:0033422" + ], + "pulmonary arterial hypertension with positive acute response to no challenge": [ + "HP:0033423" + ], + "pulmonary arterial hypertension with lack of acute response to no challenge": [ + "HP:0033424" + ], + "periungual erythema": [ + "HP:0033425" + ], + "pulmonary air embolism": [ + "HP:0033426" + ], + "venous air embolism": [ + "HP:0033426" + ], + "pulmonary capillary angioectasia": [ + "HP:0033427" + ], + "systemic autoinflammation": [ + "HP:0033428" + ], + "neuroinflammation": [ + "HP:0033429" + ], + "non - infectious meningitis": [ + "HP:0033430" + ], + "cytomegalovirus colitis": [ + "HP:0033431" + ], + "cmv colitis": [ + "HP:0033431" + ], + "opportunistic viral infection": [ + "HP:0033432" + ], + "ileocecal ulcer": [ + "HP:0033433" + ], + "ileo - cecal ulcer": [ + "HP:0033433" + ], + "nasal septum perforation": [ + "HP:0033434" + ], + "nasal - septum perforation": [ + "HP:0033434" + ], + "perforation of the nasal septum": [ + "HP:0033434" + ], + "abnormal circulate keto acid concentration": [ + "HP:0033435" + ], + "abnormal circulating keto acid concentration": [ + "HP:0033435" + ], + "elevate circulate 3 - methyl - 2 - oxovaleric acid concentration": [ + "HP:0033436" + ], + "elevated circulating 3 - methyl - 2 - oxovaleric acid concentration": [ + "HP:0033436" + ], + "elevate circulate 4 - methyl - 2 - oxopentanoic acid concentration": [ + "HP:0033437" + ], + "elevated circulating 4 - methyl - 2 - oxopentanoic acid concentration": [ + "HP:0033437" + ], + "increase circulate alpha - ketoisocaproic acid concentration": [ + "HP:0033437" + ], + "increased circulating alpha - ketoisocaproic acid concentration": [ + "HP:0033437" + ], + "elevate circulate myoglobin concentration": [ + "HP:0033438" + ], + "elevated circulating myoglobin concentration": [ + "HP:0033438" + ], + "elevate circulate decenoylcarnitine concentration": [ + "HP:0033439" + ], + "elevated circulating decenoylcarnitine concentration": [ + "HP:0033439" + ], + "elevate circulate o - decenoylcarnitine concentration": [ + "HP:0033439" + ], + "elevated circulating o - decenoylcarnitine concentration": [ + "HP:0033439" + ], + "elevate plasma decenoylcarnitine , c10:1": [ + "HP:0033439" + ], + "elevated plasma decenoylcarnitine , c10:1": [ + "HP:0033439" + ], + "elevate circulate octenoylcarnitine concentration": [ + "HP:0033440" + ], + "elevated circulating octenoylcarnitine concentration": [ + "HP:0033440" + ], + "elevate circulate o - octenoylcarnitine concentration": [ + "HP:0033440" + ], + "elevated circulating o - octenoylcarnitine concentration": [ + "HP:0033440" + ], + "elevate plasma octenoylcarnitine , c8:1": [ + "HP:0033440" + ], + "elevated plasma octenoylcarnitine , c8:1": [ + "HP:0033440" + ], + "elevate circulate hexanoylcarnitine concentration": [ + "HP:0033441" + ], + "elevated circulating hexanoylcarnitine concentration": [ + "HP:0033441" + ], + "elevate circulate o - hexanoylcarnitine concentration": [ + "HP:0033441" + ], + "elevated circulating o - hexanoylcarnitine concentration": [ + "HP:0033441" + ], + "elevate plasma hexanoylcarnitine , c6:0": [ + "HP:0033441" + ], + "elevated plasma hexanoylcarnitine , c6:0": [ + "HP:0033441" + ], + "elevate circulate glutarylcarnitine concentration": [ + "HP:0033442" + ], + "elevated circulating glutarylcarnitine concentration": [ + "HP:0033442" + ], + "elevate circulate o - glutarylcarnitine concentration": [ + "HP:0033442" + ], + "elevated circulating o - glutarylcarnitine concentration": [ + "HP:0033442" + ], + "elevate plasma glutarylcarnitine , c5 - dc": [ + "HP:0033442" + ], + "elevated plasma glutarylcarnitine , c5 - dc": [ + "HP:0033442" + ], + "elevate circulate propionylcarnitine concentration": [ + "HP:0033443" + ], + "elevated circulating propionylcarnitine concentration": [ + "HP:0033443" + ], + "elevate circulate dodecanoylcarnitine concentration": [ + "HP:0033444" + ], + "elevated circulating dodecanoylcarnitine concentration": [ + "HP:0033444" + ], + "elevate circulate o - dodecanoylcarnitine concentration": [ + "HP:0033444" + ], + "elevated circulating o - dodecanoylcarnitine concentration": [ + "HP:0033444" + ], + "elevate plasma dodecanoylcarnitine , c12:0": [ + "HP:0033444" + ], + "elevated plasma dodecanoylcarnitine , c12:0": [ + "HP:0033444" + ], + "reduce circulate acylcarnitine concentration": [ + "HP:0033445" + ], + "reduced circulating acylcarnitine concentration": [ + "HP:0033445" + ], + "elevate circulate butyrylcarnitine concentration": [ + "HP:0033446" + ], + "elevated circulating butyrylcarnitine concentration": [ + "HP:0033446" + ], + "elevate circulate o - butyrylcarnitine concentration": [ + "HP:0033446" + ], + "elevated circulating o - butyrylcarnitine concentration": [ + "HP:0033446" + ], + "elevate circulate isovalerylcarnitine concentration": [ + "HP:0033447" + ], + "elevated circulating isovalerylcarnitine concentration": [ + "HP:0033447" + ], + "elevate circulate o - isovalerylcarnitine concentration": [ + "HP:0033447" + ], + "elevated circulating o - isovalerylcarnitine concentration": [ + "HP:0033447" + ], + "increase mid - arm muscle circumference": [ + "HP:0033448" + ], + "increased mid - arm muscle circumference": [ + "HP:0033448" + ], + "decrease mid - arm muscle circumference": [ + "HP:0033449" + ], + "decreased mid - arm muscle circumference": [ + "HP:0033449" + ], + "abnormal circulate prealbumin concentration": [ + "HP:0033450" + ], + "abnormal circulating prealbumin concentration": [ + "HP:0033450" + ], + "increase circulate prealbumin concentration": [ + "HP:0033451" + ], + "increased circulating prealbumin concentration": [ + "HP:0033451" + ], + "decrease circulate prealbumin concentration": [ + "HP:0033452" + ], + "decreased circulating prealbumin concentration": [ + "HP:0033452" + ], + "limited neck extension": [ + "HP:0033453" + ], + "tube feeding": [ + "HP:0033454" + ], + "elevate urinary dicarboxylic acid level": [ + "HP:0033455" + ], + "elevated urinary dicarboxylic acid level": [ + "HP:0033455" + ], + "elevate urine keto acid level": [ + "HP:0033456" + ], + "elevated urine keto acid level": [ + "HP:0033456" + ], + "elevate urine 3 - methyl - 2 - oxovaleric acid level": [ + "HP:0033457" + ], + "elevated urine 3 - methyl - 2 - oxovaleric acid level": [ + "HP:0033457" + ], + "elevate urine 4 - methyl - 2 - oxopentanoic acid level": [ + "HP:0033458" + ], + "elevated urine 4 - methyl - 2 - oxopentanoic acid level": [ + "HP:0033458" + ], + "increase urine alpha - ketoisocaproic acid level": [ + "HP:0033458" + ], + "increased urine alpha - ketoisocaproic acid level": [ + "HP:0033458" + ], + "decrease circulate apolipoprotein concentration": [ + "HP:0033459" + ], + "decreased circulating apolipoprotein concentration": [ + "HP:0033459" + ], + "decrease apolipoprotein level": [ + "HP:0033459" + ], + "decreased apolipoprotein level": [ + "HP:0033459" + ], + "increase circulate apolipoprotein circulation": [ + "HP:0033460" + ], + "increased circulating apolipoprotein circulation": [ + "HP:0033460" + ], + "elevate circulate 3 - hydroxylinoleylcarnitine concentration": [ + "HP:0033461" + ], + "elevated circulating 3 - hydroxylinoleylcarnitine concentration": [ + "HP:0033461" + ], + "elevate plasma 3 - oh - linoleylcarnitine , c18:1 - oh": [ + "HP:0033461" + ], + "elevated plasma 3 - oh - linoleylcarnitine , c18:1 - oh": [ + "HP:0033461" + ], + "elevate circulate oleylcarnitine concentration": [ + "HP:0033462" + ], + "elevated circulating oleylcarnitine concentration": [ + "HP:0033462" + ], + "elevate plasma oleylcarnitine , c18:1": [ + "HP:0033462" + ], + "elevated plasma oleylcarnitine , c18:1": [ + "HP:0033462" + ], + "obsolete elevate circulate palmitoleylcarnitine concentration": [ + "HP:0033463" + ], + "obsolete elevated circulating palmitoleylcarnitine concentration": [ + "HP:0033463" + ], + "elevate circulate 3 - hydroxypalmitoleylcarnitine concentration": [ + "HP:0033464" + ], + "elevated circulating 3 - hydroxypalmitoleylcarnitine concentration": [ + "HP:0033464" + ], + "elevate circulate 3 - oh - palmitoleylcarnitine concentration": [ + "HP:0033464" + ], + "elevated circulating 3 - oh - palmitoleylcarnitine concentration": [ + "HP:0033464" + ], + "elevate plasma 3 - oh - palmitoleylcarnitine , c16:1 - oh": [ + "HP:0033464" + ], + "elevated plasma 3 - oh - palmitoleylcarnitine , c16:1 - oh": [ + "HP:0033464" + ], + "elevate circulate tetradecanolycarnitine concentration": [ + "HP:0033465" + ], + "elevated circulating tetradecanolycarnitine concentration": [ + "HP:0033465" + ], + "weak grip": [ + "HP:0033466" + ], + "low 10 - minute apgar score": [ + "HP:0033467" + ], + "10 - minute apgar score of 0": [ + "HP:0033468" + ], + "10 - minute apgar score of 1": [ + "HP:0033469" + ], + "10 - minute apgar score of 2": [ + "HP:0033470" + ], + "10 - minute apgar score of 3": [ + "HP:0033471" + ], + "10 - minute apgar score of 4": [ + "HP:0033472" + ], + "10 - minute apgar score of 5": [ + "HP:0033473" + ], + "10 - minute apgar score of 6": [ + "HP:0033474" + ], + "limited shoulder abduction": [ + "HP:0033475" + ], + "extractable nuclear antigen positivity": [ + "HP:0033476" + ], + "abnormal circulate lipoprotein lipase concentration": [ + "HP:0033477" + ], + "abnormal circulating lipoprotein lipase concentration": [ + "HP:0033477" + ], + "increase circulate lipoprotein lipase concentration": [ + "HP:0033478" + ], + "increased circulating lipoprotein lipase concentration": [ + "HP:0033478" + ], + "elevate lipoprotein lipase level": [ + "HP:0033478" + ], + "elevated lipoprotein lipase level": [ + "HP:0033478" + ], + "abnormal circulate bilirubin concentration": [ + "HP:0033479" + ], + "abnormal circulating bilirubin concentration": [ + "HP:0033479" + ], + "hypobilirubinemia": [ + "HP:0033480" + ], + "limited lateral neck flexion": [ + "HP:0033481" + ], + "limited shoulder flexion": [ + "HP:0033482" + ], + "podocyte infolding": [ + "HP:0033483" + ], + "elevate circulate linoleylcarnitine concentration": [ + "HP:0033484" + ], + "elevated circulating linoleylcarnitine concentration": [ + "HP:0033484" + ], + "elevate plasma linoleylcarnitine , c18:2": [ + "HP:0033484" + ], + "elevated plasma linoleylcarnitine , c18:2": [ + "HP:0033484" + ], + "glomerular basement membrane disruption": [ + "HP:0033485" + ], + "disruption of the glomerular basement membrane": [ + "HP:0033485" + ], + "glomerular basement membrane rupture": [ + "HP:0033485" + ], + "abnormal glomerular basement membrane texture": [ + "HP:0033486" + ], + "glomerular basement membrane powdery deposit": [ + "HP:0033487" + ], + "glomerular basement membranes powdery deposit": [ + "HP:0033487" + ], + "glomerular basement membrane with powdery deposit": [ + "HP:0033487" + ], + "glomerular basement membranes with powdery deposit": [ + "HP:0033487" + ], + "glomerular endocapillary leukocyte hypercellularity": [ + "HP:0033488" + ], + "glomerular endocapillary hypercellularity consist of leukocyte": [ + "HP:0033488" + ], + "glomerular endocapillary hypercellularity consisting of leukocytes": [ + "HP:0033488" + ], + "glomerular endocapillary neutrophil hypercellularity": [ + "HP:0033489" + ], + "glomerular endocapillary foam - cell hypercellularity": [ + "HP:0033490" + ], + "global mesangial sclerosis": [ + "HP:0033491" + ], + "podocyte cytoskeletal condensation": [ + "HP:0033492" + ], + "mesangial matrix expansion": [ + "HP:0033493" + ], + "increase glomerular mesangial matrix": [ + "HP:0033493" + ], + "increased glomerular mesangial matrix": [ + "HP:0033493" + ], + "glomerular basement membrane amyloid spicule": [ + "HP:0033494" + ], + "segmental glomerulosclerosis": [ + "HP:0033495" + ], + "perihilar segmental glomerulosclerosis": [ + "HP:0033496" + ], + "segmental glomerulosclerosis , perihilar pattern": [ + "HP:0033496" + ], + "tip variant segmental glomerulosclerosis": [ + "HP:0033497" + ], + "segmental glomerulosclerosis , tip variant": [ + "HP:0033497" + ], + "segmental glomerulosclerosis away from the vascular and tubular pole": [ + "HP:0033498" + ], + "segmental glomerulosclerosis away from the vascular and tubular poles": [ + "HP:0033498" + ], + "glomerular basement membrane electron dense deposit": [ + "HP:0033499" + ], + "glomerular basement membrane electron dense deposits": [ + "HP:0033499" + ], + "subendothelial glomerular basement membrane electron dense deposit": [ + "HP:0033500" + ], + "subendothelial glomerular basement membrane electron dense deposits": [ + "HP:0033500" + ], + "subepithelial glomerular basement membrane electron dense deposit": [ + "HP:0033501" + ], + "subepithelial glomerular basement membrane electron dense deposits": [ + "HP:0033501" + ], + "abnormal esterify to free carnitine ratio": [ + "HP:0033502" + ], + "abnormal esterified to free carnitine ratio": [ + "HP:0033502" + ], + "elevate csf fumarate": [ + "HP:0033503" + ], + "elevated csf fumarate": [ + "HP:0033503" + ], + "elevate circulate fumarate concentration": [ + "HP:0033504" + ], + "elevated circulating fumarate concentration": [ + "HP:0033504" + ], + "livedo reticularis": [ + "HP:0033505" + ], + "increase esterify to free carnitine 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term memory impairment": [ + "HP:0033687" + ], + "short term memory loss": [ + "HP:0033687" + ], + "long term memory impairment": [ + "HP:0033688" + ], + "long term memory loss": [ + "HP:0033688" + ], + "anterograde memory impairment": [ + "HP:0033689" + ], + "anterograde amnesia": [ + "HP:0033689" + ], + "retrograde memory impairment": [ + "HP:0033690" + ], + "retrograde amnesia": [ + "HP:0033690" + ], + "procedural memory loss": [ + "HP:0033691" + ], + "impaired procedural memory": [ + "HP:0033691" + ], + "procedural memory deficit": [ + "HP:0033691" + ], + "declarative memory loss": [ + "HP:0033692" + ], + "impaired declarative memory": [ + "HP:0033692" + ], + "phantosmia": [ + "HP:0033693" + ], + "olfactory hallucination": [ + "HP:0033693" + ], + "phantom odor": [ + "HP:0033693" + ], + "phantom odour": [ + "HP:0033693" + ], + "phantom smell": [ + "HP:0033693" + ], + "tactile hallucination": [ + "HP:0033694" + ], + "tactile hallucinations": [ + "HP:0033694" + ], + "occupational 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"grade v vur": [ + "HP:0033740" + ], + "grade iv vesicoureteral reflux": [ + "HP:0033741" + ], + "grade iv vur": [ + "HP:0033741" + ], + "intrarenal reflux": [ + "HP:0033742" + ], + "macular agenesis": [ + "HP:0033743" + ], + "global cerebellar dysplasia": [ + "HP:0033744" + ], + "dysplasia of the superior cerebellar vermis": [ + "HP:0033745" + ], + "intrascapular pain": [ + "HP:0033746" + ], + "pain between shoulder blade": [ + "HP:0033746" + ], + "pain between shoulder blades": [ + "HP:0033746" + ], + "abnormal exteroceptive sensation": [ + "HP:0033747" + ], + "hypoesthesia": [ + "HP:0033748" + ], + "hypoaesthesia": [ + "HP:0033748" + ], + "numbness": [ + "HP:0033748" + ], + "abnormal functional residual capacity": [ + "HP:0033749" + ], + "reduce functional residual capacity": [ + "HP:0033750" + ], + "reduced functional residual capacity": [ + "HP:0033750" + ], + "elevate functional residual capacity": [ + "HP:0033751" + ], + "elevated functional residual capacity": [ + "HP:0033751" 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"hutchinson incisor": [ + "HP:0033782" + ], + "semicircular tooth": [ + "HP:0033782" + ], + "tooth , semilunar": [ + "HP:0033782" + ], + "molar incisor malformation": [ + "HP:0033783" + ], + "dentin dysplasia": [ + "HP:0033784" + ], + "enamel agenesis": [ + "HP:0033785" + ], + "hypomature enamel": [ + "HP:0033786" + ], + "enamel opacity": [ + "HP:0033786" + ], + "cementum hypoplasia": [ + "HP:0033787" + ], + "cementum aplasia": [ + "HP:0033787" + ], + "cementum overgrowth": [ + "HP:0033788" + ], + "cementation hyperplasia": [ + "HP:0033788" + ], + "cementum hypertrophy": [ + "HP:0033788" + ], + "cementum overdeveloped": [ + "HP:0033788" + ], + "drumstick - shaped root": [ + "HP:0033788" + ], + "hypercementosis": [ + "HP:0033788" + ], + "trigger by cheese ingestion": [ + "HP:0033789" + ], + "triggered by cheese ingestion": [ + "HP:0033789" + ], + "thistle tube shape pulp": [ + "HP:0033790" + ], + "thistle tube shaped pulp": [ + "HP:0033790" + ], + "flame - shape pulp": [ + "HP:0033790" 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"abnormal circulate gonadal steroid concentration": [ + "HP:0033799" + ], + "abnormal circulating gonadal steroid concentration": [ + "HP:0033799" + ], + "abnormal circulate gonadocorticoid concentration": [ + "HP:0033799" + ], + "abnormal circulating gonadocorticoid concentration": [ + "HP:0033799" + ], + "abnormal circulate sex steroid concentration": [ + "HP:0033799" + ], + "abnormal circulating sex steroid concentration": [ + "HP:0033799" + ], + "blistering by anatomical location": [ + "HP:0033800" + ], + "blistering by histological location": [ + "HP:0033801" + ], + "intra - epidermal blistering": [ + "HP:0033802" + ], + "blister with sub - lamina densa plane of cleavage": [ + "HP:0033803" + ], + "blistering with sub - lamina densa plane of cleavage": [ + "HP:0033803" + ], + "subepidermal blistering": [ + "HP:0033804" + ], + "non - necrotizing granuloma": [ + "HP:0033805" + ], + "abnormal epidermis stratum granulosum morphology": [ + "HP:0033806" + ], + "absent keratohyalin granule": [ + "HP:0033807" + ], + "absent keratohyalin granules": [ + "HP:0033807" + ], + "spermatocele": [ + "HP:0033808" + ], + "increase circulate 17 hydroxypregnenolone concentration": [ + "HP:0033809" + ], + "increased circulating 17 hydroxypregnenolone concentration": [ + "HP:0033809" + ], + "decrease circulate dihydrotestosterone concentration": [ + "HP:0033810" + ], + "decreased circulating dihydrotestosterone concentration": [ + "HP:0033810" + ], + "abnormal circulate androstenedione concentration": [ + "HP:0033811" + ], + "abnormal circulating androstenedione concentration": [ + "HP:0033811" + ], + "decrease circulate androstenedione concentration": [ + "HP:0033812" + ], + "decreased circulating androstenedione concentration": [ + "HP:0033812" + ], + "perilobular": [ + "HP:0033813" + ], + "paraseptal": [ + "HP:0033814" + ], + "bronchocentric": [ + "HP:0033815" + ], + "centrilobular": [ + "HP:0033816" + ], + "miliary": [ + "HP:0033817" + ], + "reticular": [ + "HP:0033818" + ], 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"oculomotor synkinesis": [ + "HP:0033851" + ], + "abnormal intrarenal vein morphology": [ + "HP:0033852" + ], + "abnormal arcuate vein morphology": [ + "HP:0033853" + ], + "abnormal interlobular vein morphology": [ + "HP:0033854" + ], + "abnormal interlobular vein lumen morphology": [ + "HP:0033855" + ], + "abnormal morphology of the interlobular vein lumen": [ + "HP:0033855" + ], + "cholesterol embolus within interlobular vein lumen": [ + "HP:0033856" + ], + "cholesterol emboli within interlobular vein lumen": [ + "HP:0033856" + ], + "intraluminal thrombus within interlobular vein": [ + "HP:0033857" + ], + "intraluminal thrombi within interlobular veins": [ + "HP:0033857" + ], + "organize thrombus within interlobular vein lumen": [ + "HP:0033858" + ], + "organized thrombi within interlobular vein lumen": [ + "HP:0033858" + ], + "abnormal peritubular capillary morphology": [ + "HP:0033859" + ], + "abnormal cortical peritubular capillary morphology": [ + "HP:0033860" + ], + "multilamellation of cortical peritubular capillary basement membrane": [ + "HP:0033861" + ], + "multilamellation of cortical peritubular capillary basement membranes": [ + "HP:0033861" + ], + "multilamellation of basement membrane within cortical peritubular capillary": [ + "HP:0033861" + ], + "multilamellation of basement membranes within cortical peritubular capillaries": [ + "HP:0033861" + ], + "cortical peritubular capillaritis": [ + "HP:0033862" + ], + "abnormal cortical peritubular capillary lumen morphology": [ + "HP:0033863" + ], + "abnormal medullary peritubular capillary morphology": [ + "HP:0033864" + ], + "medullary peritubular capillaritis": [ + "HP:0033865" + ], + "medullary peritubular capillary erythrocyte congestion": [ + "HP:0033866" + ], + "multilamellation of medullary peritubular capillary basement membrane": [ + "HP:0033867" + ], + "multilamellation of medullary peritubular capillary basement membranes": [ + "HP:0033867" + ], + "multilamellation of basement membrane within medullary peritubular capillary": [ + "HP:0033867" + ], + "multilamellation of basement membranes within medullary peritubular capillaries": [ + "HP:0033867" + ], + "abnormal medullary peritubular capillary lumen morphology": [ + "HP:0033868" + ], + "medullary peritubular capillary lumen cholesterol embolus": [ + "HP:0033869" + ], + "medullary peritubular capillary lumen cholesterol emboli": [ + "HP:0033869" + ], + "cholesterol embolus within the medullary peritubular capillary lumen": [ + "HP:0033869" + ], + "cholesterol emboli within the medullary peritubular capillary lumen": [ + "HP:0033869" + ], + "medullary peritubular capillary intraluminal thrombus": [ + "HP:0033870" + ], + "medullary peritubular capillary intraluminal thrombi": [ + "HP:0033870" + ], + "intraluminal thrombus within medullary peritubular capillary": [ + "HP:0033870" + ], + "intraluminal thrombi within medullary peritubular capillaries": [ + "HP:0033870" + ], + "medullary peritubular capillary lumen organize thrombus": [ + "HP:0033871" + ], + "medullary peritubular capillary lumen organized thrombi": [ + "HP:0033871" + ], + "organize thrombus within the medullary peritubular capillary lumen": [ + "HP:0033871" + ], + "organized thrombi within the medullary peritubular capillary lumen": [ + "HP:0033871" + ], + "cortical peritubular capillary lumen cholesterol embolus": [ + "HP:0033872" + ], + "cortical peritubular capillary lumen cholesterol emboli": [ + "HP:0033872" + ], + "cortical peritubular capillary intraluminal thrombus": [ + "HP:0033873" + ], + "cortical peritubular capillary intraluminal thrombi": [ + "HP:0033873" + ], + "intraluminal thrombus within cortical peritubular capillary": [ + "HP:0033873" + ], + "intraluminal thrombi within cortical peritubular capillaries": [ + "HP:0033873" + ], + "cortical peritubular capillary lumen organize thrombus": [ + "HP:0033874" + ], + "cortical peritubular capillary lumen organized thrombi": [ + "HP:0033874" + ], + "abnormal arcuate vein lumen morphology": [ + "HP:0033875" + ], + "arcuate vein lumen cholesterol embolus": [ + "HP:0033876" + ], + "arcuate vein lumen cholesterol emboli": [ + "HP:0033876" + ], + "cholesterol embolus within arcuate vein lumen": [ + "HP:0033876" + ], + "cholesterol emboli within arcuate vein lumen": [ + "HP:0033876" + ], + "arcuate vein intraluminal thrombus": [ + "HP:0033877" + ], + "arcuate vein intraluminal thrombi": [ + "HP:0033877" + ], + "intraluminal thrombus within arcuate vein": [ + "HP:0033877" + ], + "intraluminal thrombi within arcuate veins": [ + "HP:0033877" + ], + "arcuate vein lumen organize thrombus": [ + "HP:0033878" + ], + "arcuate vein lumen organized thrombi": [ + "HP:0033878" + ], + "organize thrombus within arcuate vein lumen": [ + "HP:0033878" + ], + "organized thrombi within arcuate vein lumen": [ + "HP:0033878" + ], + "abnormal arcuate vein intima / medium morphology": [ + "HP:0033879" + ], + "abnormal arcuate vein intima / media morphology": [ + "HP:0033879" + ], + "arcuate vein intimal mucoid edema": [ + "HP:0033880" + ], + "intimal mucoid edema within arcuate vein": [ + "HP:0033880" + ], + "intimal mucoid edema within arcuate veins": [ + "HP:0033880" + ], + "arcuate vein intimal / medial myxomatous degeneration": [ + "HP:0033881" + ], + "myxomatous change within arcuate vein intima / medium": [ + "HP:0033881" + ], + "myxomatous change within arcuate vein intima / media": [ + "HP:0033881" + ], + "arcuate vein intima / medial amyloidosis": [ + "HP:0033882" + ], + "amyloidosis within arcuate vein intima / medium": [ + "HP:0033882" + ], + "amyloidosis within arcuate vein intima / media": [ + "HP:0033882" + ], + "abnormal cortical radial artery morphology": [ + "HP:0033883" + ], + "abnormal interlobular artery morphology": [ + "HP:0033883" + ], + "abnormal cortical radial artery lumen morphology": [ + "HP:0033884" + ], + "abnormal interlobular arterial lumen morphology": [ + "HP:0033884" + ], + "cortical radial artery lumen 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plasma apolipoprotein c - ii": [ + "HP:0033983" + ], + "decreased plasma apolipoprotein c - ii": [ + "HP:0033983" + ], + "increase urinary 8 - oxo - 7,8 - dihydroguanosine level": [ + "HP:0033984" + ], + "increased urinary 8 - oxo - 7,8 - dihydroguanosine level": [ + "HP:0033984" + ], + "increase urinary 8 - oxo - 7,8 - dihydroguanosine": [ + "HP:0033984" + ], + "increased urinary 8 - oxo - 7,8 - dihydroguanosine": [ + "HP:0033984" + ], + "increase urinary 8 - oxo - gsn level": [ + "HP:0033984" + ], + "increased urinary 8 - oxo - gsn level": [ + "HP:0033984" + ], + "increase urine 8 - oxo - 7,8 - dihydroguanosine": [ + "HP:0033984" + ], + "increased urine 8 - oxo - 7,8 - dihydroguanosine": [ + "HP:0033984" + ], + "increase urine 8 - oxo - gmp": [ + "HP:0033984" + ], + "increased urine 8 - oxo - gmp": [ + "HP:0033984" + ], + "elongate femoral neck": [ + "HP:0033985" + ], + "elongated femoral neck": [ + "HP:0033985" + ], + "long femoral neck": [ + "HP:0033985" + ], + "tortuous lymphatic 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], + "bronchial hemorrhage": [ + "HP:0033999" + ], + "bronchial bleeding": [ + "HP:0033999" + ], + "tracheal hemorrhage": [ + "HP:0034000" + ], + "tracheal bleeding": [ + "HP:0034000" + ], + "anti - complement factor h antibody positivity": [ + "HP:0034001" + ], + "cfh autoantibody": [ + "HP:0034001" + ], + "cfh autoantibodies": [ + "HP:0034001" + ], + "anti - phospholipase a2 receptor antibody positivity": [ + "HP:0034002" + ], + "anti - pla2r antibody positivity": [ + "HP:0034002" + ], + "broad medial eyebrow": [ + "HP:0034003" + ], + "medial broadening of eyebrow": [ + "HP:0034003" + ], + "medial broadening of eyebrows": [ + "HP:0034003" + ], + "parosmia": [ + "HP:0034004" + ], + "decrease dendritic spine number": [ + "HP:0034005" + ], + "decreased dendritic spine number": [ + "HP:0034005" + ], + "decrease urinary lysyl - pyridinoline - hydroxylysyl - pyridinoline ratio": [ + "HP:0034006" + ], + "decreased urinary lysyl - pyridinoline - hydroxylysyl - pyridinoline ratio": [ + "HP:0034006" + ], + "posterior atrophy of corpus callosum": [ + "HP:0034007" + ], + "opto - chiasmatic atrophy": [ + "HP:0034008" + ], + "pelvic lipomatosis": [ + "HP:0034009" + ], + "increase megakaryocyte colony form unit count": [ + "HP:0034010" + ], + "increased megakaryocyte colony forming unit count": [ + "HP:0034010" + ], + "reduce progressive sperm motility": [ + "HP:0034011" + ], + "reduced progressive sperm motility": [ + "HP:0034011" + ], + "non - progressive sperm motility": [ + "HP:0034011" + ], + "palmoplantar hypohidrosis": [ + "HP:0034012" + ], + "curvilinear pericallosal lipoma": [ + "HP:0034013" + ], + "tubulonodular pericallosal lipoma": [ + "HP:0034014" + ], + "cavitating pulmonary nodule": [ + "HP:0034015" + ], + "anti - hla antibody positivity": [ + "HP:0034016" + ], + "anti - human leukocyte antigen antibody positivity": [ + "HP:0034016" + ], + "anti - class i hla antibody positivity": [ + "HP:0034017" + ], + "anti - class ii hla antibody positivity": [ + "HP:0034018" + ], + "anti - hla - a antibody positivity": [ + "HP:0034019" + ], + "anti - hla - a igg1 antibody positivity": [ + "HP:0034020" + ], + "anti - hla - a igg3 antibody positivity": [ + "HP:0034021" + ], + "anti - hla - b antibody positivity": [ + "HP:0034022" + ], + "anti - hla - b igg1 antibody positivity": [ + "HP:0034023" + ], + "anti - hla - b igg3 antibody positivity": [ + "HP:0034024" + ], + "abnormal circulate gaba concentration": [ + "HP:0034025" + ], + "abnormal circulating gaba concentration": [ + "HP:0034025" + ], + "elevate circulate sacchoropine concentration": [ + "HP:0034026" + ], + "elevated circulating sacchoropine concentration": [ + "HP:0034026" + ], + "abnormal urinary non - proteinogenic amino acid level": [ + "HP:0034027" + ], + "saccharopinuria": [ + "HP:0034028" + ], + "hepatic foam cell": [ + "HP:0034029" + ], + "hepatic foam cells": [ + "HP:0034029" + ], + "lip cyanosis": [ + "HP:0034030" + ], + "bluish lip": [ + "HP:0034030" + ], + "bluish lips": [ + "HP:0034030" + ], + "cyanotic lip": [ + "HP:0034030" + ], + "cyanotic lips": [ + "HP:0034030" + ], + "labial cyanosis": [ + "HP:0034030" + ], + "facial cyanosis": [ + "HP:0034031" + ], + "bluish face": [ + "HP:0034031" + ], + "cyanotic face": [ + "HP:0034031" + ], + "central cyanosis": [ + "HP:0034032" + ], + "peripheral cyanosis": [ + "HP:0034033" + ], + "differential cyanosis": [ + "HP:0034034" + ], + "pharyngeal exudate": [ + "HP:0034035" + ], + "fluid from the pharynx": [ + "HP:0034035" + ], + "pharyngeal fluid": [ + "HP:0034035" + ], + "pseudo - chilblain on toe": [ + "HP:0034036" + ], + "pseudo - chilblains on toes": [ + "HP:0034036" + ], + "chilblain - like toe lesion": [ + "HP:0034036" + ], + "chilblain - like toe lesions": [ + "HP:0034036" + ], + "chilblain - like toe": [ + "HP:0034036" + ], + "chilblain - like toes": [ + "HP:0034036" + ], + "covid toe": [ + "HP:0034036" + ], + "pseudo - chilblain on finger": [ + "HP:0034037" + ], + "pseudo - chilblains on fingers": [ + "HP:0034037" + ], + "covid finger": [ + "HP:0034037" + ], + "covid fingers": [ + "HP:0034037" + ], + "silent hypoxemia": [ + "HP:0034038" + ], + "ventricular couplet": [ + "HP:0034039" + ], + "doublet premature ventricular contraction": [ + "HP:0034039" + ], + "doublet premature ventricular contractions": [ + "HP:0034039" + ], + "bidirectional ventricular tachycardia": [ + "HP:0034040" + ], + "ventricular ectopy": [ + "HP:0034041" + ], + "dorsal hirsutism": [ + "HP:0034042" + ], + "abnormality of corneal shape": [ + "HP:0040004" + ], + "mortality / age": [ + "HP:0040006" + ], + "mortality / aging": [ + "HP:0040006" + ], + "absent pigmentation of chest": [ + "HP:0040007" + ], + "lack of skin color on chest": [ + "HP:0040007" + ], + "lack of skin coloring on chest": [ + "HP:0040007" + ], + "lack of skin colour on chest": [ + "HP:0040007" + ], + "lack of skin colouring on chest": [ + "HP:0040007" + ], + "aplasia of facial bone": [ + "HP:0040008" + ], + "aplasia of facial bones": [ + "HP:0040008" + ], + "absence of facial bone": [ + "HP:0040008" + ], + "absence of facial bones": [ + "HP:0040008" + ], + "agenesis of facial bone": [ + "HP:0040008" + ], + "agenesis of facial bones": [ + "HP:0040008" + ], + "aplasia of facial skeleton": [ + "HP:0040008" + ], + "failure of development of facial bone": [ + "HP:0040008" + ], + "failure of development of facial bones": [ + "HP:0040008" + ], + "failure of development of facial skeleton": [ + "HP:0040008" + ], + "miss facial bone": [ + "HP:0040008" + ], + "missing facial bones": [ + "HP:0040008" + ], + "hyperparakeratosis": [ + "HP:0040009" + ], + "small posterior fossa": [ + "HP:0040010" + ], + "flat posterior fossa": [ + "HP:0040011" + ], + "chromosome breakage": [ + "HP:0040012" + ], + "high frequency of chromosome break in lymphocyte": [ + "HP:0040012" + ], + "high frequency of chromosome breaks in lymphocytes": [ + "HP:0040012" + ], + "increase chromosomal breakage": [ + "HP:0040012" + ], + "increased chromosomal breakage": [ + "HP:0040012" + ], + "increase chromosomal breakage rate": [ + "HP:0040012" + ], + "increased chromosomal breakage rate": [ + "HP:0040012" + ], + "multiple chromosomal break": [ + "HP:0040012" + ], + "multiple chromosomal breaks": [ + "HP:0040012" + ], + "tendency to chromosomal breakage": [ + "HP:0040012" + ], + "decrease mitochondrial number": [ + "HP:0040013" + ], + "decreased mitochondrial number": [ + "HP:0040013" + ], + "increase mitochondrial number": [ + "HP:0040014" + ], + "increased mitochondrial number": [ + "HP:0040014" + ], + "increased activity of mitochondrial respiratory chain": [ + "HP:0040015" + ], + "prominent coccyx": [ + "HP:0040016" + ], + "prominent tailbone": [ + "HP:0040016" + ], + "protrude coccyx": [ + "HP:0040017" + ], + "protruding coccyx": [ + "HP:0040017" + ], + "protrude tailbone": [ + "HP:0040017" + ], + "protruding tailbone": [ + "HP:0040017" + ], + "clinodactyly of hallux": [ + "HP:0040018" + ], + "curvature of big toe": [ + "HP:0040018" + ], + "finger clinodactyly": [ + "HP:0040019" + ], + "curvature of finger": [ + "HP:0040019" + ], + "radial deviation of the 5th finger": [ + "HP:0040020" + ], + "radial deviation of the thumb": [ + "HP:0040021" + ], + "clinodactyly of the 2nd finger": [ + "HP:0040022" + ], + "curvature of index finger": [ + "HP:0040022" + ], + "second finger clinodactyly": [ + "HP:0040022" + ], + "clinodactyly of the thumb": [ + "HP:0040023" + ], + "curvature of thumb": [ + "HP:0040023" + ], + "clinodactyly of the 3rd finger": [ + "HP:0040024" + ], + "curvature of middle finger": [ + "HP:0040024" + ], + "clinodactyly of the 4th finger": [ + "HP:0040025" + ], + "curvature of ring finger": [ + "HP:0040025" + ], + "chorioretinal hypopigmentation": [ + "HP:0040030" + ], + "chorioretinal hyperpigmentation": [ + "HP:0040031" + ], + "hypoplasia of the upper eyelid": [ + "HP:0040032" + ], + "hypoplasia of the upper eyelids": [ + "HP:0040032" + ], + "decreased size of upper eyelid": [ + "HP:0040032" + ], + "hypotrophic upper eyelid": [ + "HP:0040032" + ], + "short upper eyelid": [ + "HP:0040032" + ], + "small upper eyelid": [ + "HP:0040032" + ], + "underdevelopment of upper eyelid": [ + "HP:0040032" + ], + "aplasia / hypoplasia of the fifth metatarsal bone": [ + "HP:0040033" + ], + "absent / small 5th long bone of foot": [ + "HP:0040033" + ], + "absent / underdevelop 5th long bone of foot": [ + "HP:0040033" + ], + "absent / underdeveloped 5th long bone of foot": [ + "HP:0040033" + ], + "abnormality of the second metatarsal bone": [ + "HP:0040034" + ], + "abnormality of the 2nd long bone of foot": [ + "HP:0040034" + ], + "abnormality of the fourth metatarsal bone": [ + "HP:0040035" + ], + "abnormality of the 4th long bone of foot": [ + "HP:0040035" + ], + "onychogryposis of fingernail": [ + "HP:0040036" + ], + "overgrowth and curving of fingernail": [ + "HP:0040036" + ], + "obsolete thin fingernail ( obsolete )": [ + "HP:0040037" + ], + "obsolete thin toenail": [ + "HP:0040038" + ], + "onycholysis of fingernail": [ + "HP:0040039" + ], + "onycholysis of fingernails": [ + "HP:0040039" + ], + "detachment of fingernail": [ + "HP:0040039" + ], + "detachment of fingernails": [ + "HP:0040039" + ], + "toenail onycholysis": [ + "HP:0040040" + ], + "detachment of toenail": [ + "HP:0040040" + ], + "detachment of toenails": [ + "HP:0040040" + ], + "onycholysis of toenail": [ + "HP:0040040" + ], + "onycholysis of toenails": [ + "HP:0040040" + ], + "aplasia of the eccrine sweat gland": [ + "HP:0040042" + ], + "aplasia of the eccrine sweat glands": [ + "HP:0040042" + ], + "absent eccrine sweat gland": [ + "HP:0040042" + ], + "absent eccrine sweat glands": [ + "HP:0040042" + ], + "hypoplasia of the eccrine sweat gland": [ + "HP:0040043" + ], + "hypoplasia of the eccrine sweat glands": [ + "HP:0040043" + ], + "underdeveloped major sweat gland": [ + "HP:0040043" + ], + "underdeveloped major sweat glands": [ + "HP:0040043" + ], + "hypoplasia of the diaphragm": [ + "HP:0040044" + ], + "underdeveloped diaphragm": [ + "HP:0040044" + ], + "abnormal hemidiaphragm morphology": [ + "HP:0040045" + ], + "abnormality of the hemidiaphragms": [ + "HP:0040045" + ], + "abnormal leave hemidiaphragm morphology": [ + "HP:0040046" + ], + "abnormal left hemidiaphragm morphology": [ + "HP:0040046" + ], + "abnormality of the left hemidiaphragm": [ + "HP:0040046" + ], + "abnormal right hemidiaphragm morphology": [ + "HP:0040047" + ], + "abnormality of the right hemidiaphragm": [ + "HP:0040047" + ], + "obsolete aplasia of the left hemidiaphragm": [ + "HP:0040048" + ], + "macular edema": [ + "HP:0040049" + ], + "macular oedema": [ + "HP:0040049" + ], + "sparse upper eyelash": [ + "HP:0040050" + ], + "sparse upper eyelashes": [ + "HP:0040050" + ], + "hypotrichosis of upper eyelash": [ + "HP:0040050" + ], + "hypotrichosis of upper eyelashes": [ + "HP:0040050" + ], + "partial absence of upper eyelash": [ + "HP:0040050" + ], + "partial absence of upper eyelashes": [ + "HP:0040050" + ], + "abnormality of upper eyelash": [ + "HP:0040051" + ], + "abnormality of upper eyelashes": [ + "HP:0040051" + ], + "abnormality of low eyelash": [ + "HP:0040052" + ], + "abnormality of lower eyelashes": [ + "HP:0040052" + ], + "long low eyelash": [ + "HP:0040053" + ], + "long lower eyelashes": [ + "HP:0040053" + ], + "ciliary trichomegaly of low eyelash": [ + "HP:0040053" + ], + "ciliary trichomegaly of lower eyelashes": [ + "HP:0040053" + ], + "increased length of low eyelash": [ + "HP:0040053" + ], + "increased length of lower eyelashes": [ + "HP:0040053" + ], + "short upper eyelash": [ + "HP:0040054" + ], + "short upper eyelashes": [ + "HP:0040054" + ], + "decreased length of upper eyelash": [ + "HP:0040054" + ], + "decreased length of upper eyelashes": [ + "HP:0040054" + ], + "short low eyelash": [ + "HP:0040055" + ], + "short lower eyelashes": [ + "HP:0040055" + ], + "decreased length of low eyelash": [ + "HP:0040055" + ], + "decreased length of lower eyelashes": [ + "HP:0040055" + ], + "absent upper eyelash": [ + "HP:0040056" + ], + "absent upper eyelashes": [ + "HP:0040056" + ], + "agenesis of upper eyelash": [ + "HP:0040056" + ], + "agenesis of upper eyelashes": [ + "HP:0040056" + ], + "aplasia of upper eyelash": [ + "HP:0040056" + ], + "aplasia of upper eyelashes": [ + "HP:0040056" + ], + "atrichia of upper eyelash": [ + "HP:0040056" + ], + "atrichia of upper eyelashes": [ + "HP:0040056" + ], + "failure of development of upper eyelash": [ + "HP:0040056" + ], + "failure of development of upper eyelashes": [ + "HP:0040056" + ], + "abnormality of nasal hair": [ + "HP:0040057" + ], + "abnormality of nose hair": [ + "HP:0040057" + ], + "calcification of rib": [ + "HP:0040059" + ], + "calcification of ribs": [ + "HP:0040059" + ], + "osteosclerosis of the radius": [ + "HP:0040061" + ], + "slender radius": [ + "HP:0040062" + ], + "decrease adipose tissue": [ + "HP:0040063" + ], + "decreased adipose tissue": [ + "HP:0040063" + ], + "decrease fat tissue": [ + "HP:0040063" + ], + "decreased fat tissue": [ + "HP:0040063" + ], + "abnormality of limb": [ + "HP:0040064" + ], + "abnormality of limbs": [ + "HP:0040064" + ], + "abnormal limb": [ + "HP:0040064" + ], + "abnormal limbs": [ + "HP:0040064" + ], + "dysmelia": [ + "HP:0040064" + ], + "limb anomaly": [ + "HP:0040064" + ], + "obsolete abnormal morphology of bone of the upper limb": [ + "HP:0040065" + ], + "obsolete abnormal morphology of bones of the upper limbs": [ + "HP:0040065" + ], + "obsolete abnormal morphology of bone of the low limb": [ + "HP:0040066" + ], + "obsolete abnormal morphology of bones of the lower limbs": [ + "HP:0040066" + ], + "abnormality of limb bone": [ + "HP:0040068" + ], + "abnormal low limb bone morphology": [ + "HP:0040069" + ], + "abnormal lower limb bone morphology": [ + "HP:0040069" + ], + "abnormal morphology of bone of the low limb": [ + "HP:0040069" + ], + "abnormal morphology of bones of the lower limbs": [ + "HP:0040069" + ], + "abnormal shape of bone of the low limb": [ + "HP:0040069" + ], + "abnormal shape of bones of the lower limbs": [ + "HP:0040069" + ], + "abnormality of low limb bone": [ + "HP:0040069" + ], + "abnormality of lower limb bone": [ + "HP:0040069" + ], + "abnormal upper limb bone morphology": [ + "HP:0040070" + ], + "abnormal morphology of bone of the upper limb": [ + "HP:0040070" + ], + "abnormal morphology of bones of the upper limbs": [ + "HP:0040070" + ], + "abnormal shape of bone of the upper limb": [ + "HP:0040070" + ], + "abnormal shape of bones of the upper limbs": [ + "HP:0040070" + ], + "abnormality of upper limb bone": [ + "HP:0040070" + ], + "abnormal morphology of ulna": [ + "HP:0040071" + ], + "abnormality of forearm bone": [ + "HP:0040072" + ], + "abnormal forearm bone morphology": [ + "HP:0040073" + ], + "abnormal shape of of forearm bone": [ + "HP:0040073" + ], + "hypopituitarism": [ + "HP:0040075" + ], + "obsolete abnormal concentration of calcium in blood": [ + "HP:0040077" + ], + "axonal degeneration": [ + "HP:0040078" + ], + "irregular dentition": [ + "HP:0040079" + ], + "irregular teeth": [ + "HP:0040079" + ], + "anteverted ear": [ + "HP:0040080" + ], + "anteverted ears": [ + "HP:0040080" + ], + "abnormal circulate creatine kinase concentration": [ + "HP:0040081" + ], + "abnormal circulating creatine kinase concentration": [ + "HP:0040081" + ], + "abnormal circulate ck concentration": [ + "HP:0040081" + ], + "abnormal circulating ck concentration": [ + "HP:0040081" + ], + "abnormal circulate cpk concentration": [ + "HP:0040081" + ], + "abnormal circulating cpk concentration": [ + "HP:0040081" + ], + "abnormal circulation phospho - ck concentration": [ + "HP:0040081" + ], + "abnormal level of creatine kinase in blood": [ + "HP:0040081" + ], + "abnormal levels of creatine kinase in blood": [ + "HP:0040081" + ], + "happy demeanor": [ + "HP:0040082" + ], + "happy demeanour": [ + "HP:0040082" + ], + "toe walk": [ + "HP:0040083" + ], + "toe walking": [ + "HP:0040083" + ], + "toe - walking": [ + "HP:0040083" + ], + "abnormal circulating renin": [ + "HP:0040084" + ], + "abnormal plasma renin": [ + "HP:0040084" + ], + "abnormal circulate aldosterone": [ + "HP:0040085" + ], + "abnormal circulating aldosterone": [ + "HP:0040085" + ], + "abnormal plasma aldosterone": [ + "HP:0040085" + ], + "abnormal prolactin level": [ + "HP:0040086" + ], + "abnormal blood folate concentration": [ + "HP:0040087" + ], + "abnormal serum folate": [ + "HP:0040087" + ], + "abnormality of folate in blood": [ + "HP:0040087" + ], + "abnormal lymphocyte count": [ + "HP:0040088" + ], + "abnormal lymphocyte counts": [ + "HP:0040088" + ], + "abnormal number of lymphocyte": [ + "HP:0040088" + ], + "abnormal number of lymphocytes": [ + "HP:0040088" + ], + "abnormal numbers of lymphocytes": [ + "HP:0040088" + ], + "abnormality of lymphocyte number": [ + "HP:0040088" + ], + "abnormal natural killer cell count": [ + "HP:0040089" + ], + "abnormal nk cell count": [ + "HP:0040089" + ], + "abnormal number of natural killer cell": [ + "HP:0040089" + ], + "abnormal number of natural killer cells": [ + "HP:0040089" + ], + "abnormality of natural killer cell count": [ + "HP:0040089" + ], + "abnormality of the tympanic membrane": [ + "HP:0040090" + ], + "abnormality of the eardrum": [ + "HP:0040090" + ], + "asymmetry of the size of ear": [ + "HP:0040091" + ], + "asymmetry of the size of ears": [ + "HP:0040091" + ], + "asymmetry of the shape of the ear": [ + "HP:0040092" + ], + "asymmetry of the shape of the ears": [ + "HP:0040092" + ], + "asymmetry of the position of the ear": [ + "HP:0040093" + ], + "asymmetry of the position of the ears": [ + "HP:0040093" + ], + "uneven ear": [ + "HP:0040093" + ], + "uneven ears": [ + "HP:0040093" + ], + "neoplasm of the outer ear": [ + "HP:0040095" + ], + "outer ear tumor": [ + "HP:0040095" + ], + "outer ear tumour": [ + "HP:0040095" + ], + "neoplasm of the inner ear": [ + "HP:0040096" + ], + "inner ear tumor": [ + "HP:0040096" + ], + "inner ear tumour": [ + "HP:0040096" + ], + "neoplasm of the ceruminal gland": [ + "HP:0040097" + ], + "adenoma of the ceruminous gland": [ + "HP:0040097" + ], + "ceruminoma": [ + "HP:0040097" + ], + "ceruminous adenoma": [ + "HP:0040097" + ], + "basalioma of the outer ear": [ + "HP:0040098" + ], + "abnormality of the round window": [ + "HP:0040099" + ], + "abnormality of the vestibular window": [ + "HP:0040100" + ], + "abnormality of the oval window": [ + "HP:0040100" + ], + "cutaneous atresia of the external auditory canal": [ + "HP:0040101" + ], + "osseous atresia of the external auditory canal": [ + "HP:0040102" + ], + "cutaneous stenosis of the external auditory canal": [ + "HP:0040103" + ], + "osseous stenosis of the external auditory canal": [ + "HP:0040104" + ], + "morphological abnormality of the lateral semicircular canal": [ + "HP:0040106" + ], + "morphological abnormality of the horizontal semicircular canal": [ + "HP:0040106" + ], + "morphological abnormality of the posterior semicircular canal": [ + "HP:0040107" + ], + "morphological abnormality of the anterior semicircular canal": [ + "HP:0040108" + ], + "morphological abnormality of the utricle": [ + "HP:0040109" + ], + "morphological abnormality of the saccule": [ + "HP:0040110" + ], + "bilateral external ear deformity": [ + "HP:0040111" + ], + "abnormal number of tubercle": [ + "HP:0040112" + ], + "abnormal number of tubercles": [ + "HP:0040112" + ], + "old - age sensorineural hearing impairment": [ + "HP:0040113" + ], + "old - aged sensorineural hearing impairment": [ + "HP:0040113" + ], + "presbycusis": [ + "HP:0040113" + ], + "absence of the reflex of the tensor tympani muscle": [ + "HP:0040114" + ], + "abnormality of the eustachian tube": [ + "HP:0040115" + ], + "aplasia of the eustachian tube": [ + "HP:0040116" + ], + "absent eustachian tube": [ + "HP:0040116" + ], + "atresia of the eustachian tube": [ + "HP:0040117" + ], + "stenosis of the eustachian tube": [ + "HP:0040118" + ], + "unilateral conductive hearing impairment": [ + "HP:0040119" + ], + "abnormality of the reflex of the tensor tympani muscle": [ + "HP:0040120" + ], + "abnormality of the acoustic reflex": [ + "HP:0040121" + ], + "abnormal auditory reflex": [ + "HP:0040121" + ], + "abnormal middle - ear - muscle ( mem ) reflex": [ + "HP:0040121" + ], + "abnormal middle - ear - muscles ( mem ) reflex": [ + "HP:0040121" + ], + "abnormality of stapedial reflex": [ + "HP:0040121" + ], + "impairment of the the acoustic reflex": [ + "HP:0040122" + ], + "impairment of the reflex of the tensor tympani muscle": [ + "HP:0040123" + ], + "patent tuba eustachii": [ + "HP:0040124" + ], + "open tuba eustachii": [ + "HP:0040124" + ], + "abnormal vitamin b12 level": [ + "HP:0040126" + ], + "abnormal serum cobalamin level": [ + "HP:0040126" + ], + "abnormal sweat homeostasis": [ + "HP:0040127" + ], + "abnormal sweat electrolyte": [ + "HP:0040128" + ], + "abnormal sweat electrolytes": [ + "HP:0040128" + ], + "abnormal 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intestines": [ + "HP:0040273" + ], + "adenocarcinoma of the small intestine": [ + "HP:0040274" + ], + "adenocarcinoma of the large intestine": [ + "HP:0040275" + ], + "adenocarcinoma of the colon": [ + "HP:0040276" + ], + "neoplasm of the pituitary gland": [ + "HP:0040277" + ], + "prolactinoma": [ + "HP:0040278" + ], + "frequency": [ + "HP:0040279" + ], + "obligate": [ + "HP:0040280" + ], + "obligate ( 100 % )": [ + "HP:0040280" + ], + "very frequent": [ + "HP:0040281" + ], + "very frequent ( 99 - 80 % )": [ + "HP:0040281" + ], + "frequent": [ + "HP:0040282" + ], + "frequent ( 79 - 30 % )": [ + "HP:0040282" + ], + "occasional": [ + "HP:0040283" + ], + "occasional ( 29 - 5 % )": [ + "HP:0040283" + ], + "very rare": [ + "HP:0040284" + ], + "very rare ( & lt ; 4 - 1 % )": [ + "HP:0040284" + ], + "very rare ( < 4 - 1 % )": [ + "HP:0040284" + ], + "exclude": [ + "HP:0040285" + ], + "excluded": [ + "HP:0040285" + ], + "exclude ( 0 % )": [ + "HP:0040285" + ], + "excluded ( 0 % )": [ + 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tongue": [ + "HP:0040294" + ], + "duplication of tongue": [ + "HP:0040294" + ], + "tongue duplicate": [ + "HP:0040294" + ], + "tongue duplicated": [ + "HP:0040294" + ], + "tongue duplication": [ + "HP:0040294" + ], + "duplication of the upper lip": [ + "HP:0040295" + ], + "double upper lip": [ + "HP:0040295" + ], + "abnormal location of the eyebrow": [ + "HP:0040296" + ], + "abnormal location of eyebrow": [ + "HP:0040296" + ], + "abnormal location of eyebrows": [ + "HP:0040296" + ], + "abnormally place eyebrow": [ + "HP:0040296" + ], + "abnormally placed eyebrows": [ + "HP:0040296" + ], + "preauricular cyst": [ + "HP:0040297" + ], + "hyperplasia of the endometrium": [ + "HP:0040298" + ], + "hyperplastic endometrium": [ + "HP:0040298" + ], + "decrease circulate free fatty acid level": [ + "HP:0040299" + ], + "decreased circulating free fatty acid level": [ + "HP:0040299" + ], + "low fatty acid level": [ + "HP:0040299" + ], + "low fatty acids level": [ + "HP:0040299" + ], + "abnormal circulate free fatty acid concentration": [ + "HP:0040300" + ], + "abnormal circulating free fatty acid concentration": [ + "HP:0040300" + ], + "abnormal circulate free fatty acid level": [ + "HP:0040300" + ], + "abnormal circulating free fatty acid level": [ + "HP:0040300" + ], + "increase urinary glycerol": [ + "HP:0040301" + ], + "increased urinary glycerol": [ + "HP:0040301" + ], + "hyperglycerolemia": [ + "HP:0040302" + ], + "pseudohypertriglyceridemia": [ + "HP:0040302" + ], + "decrease serum iron": [ + "HP:0040303" + ], + "decreased serum iron": [ + "HP:0040303" + ], + "low serum iron": [ + "HP:0040303" + ], + "duplication of the sella turcica": [ + "HP:0040304" + ], + "duplicate sella turcica": [ + "HP:0040304" + ], + "duplicated sella turcica": [ + "HP:0040304" + ], + "increase male libido": [ + "HP:0040305" + ], + "increased male libido": [ + "HP:0040305" + ], + "decrease male libido": [ + "HP:0040306" + ], + "decreased male libido": [ + "HP:0040306" + ], + "male sexual dysfunction": [ + "HP:0040307" + ], + "male anorgasmia": [ + "HP:0040308" + ], + "increase size of the mandible": [ + "HP:0040309" + ], + "increased size of the mandible": [ + "HP:0040309" + ], + "large jaw": [ + "HP:0040309" + ], + "sterile arthritis": [ + "HP:0040310" + ], + "symmetric polyarthritis": [ + "HP:0040311" + ], + "temporomandibular arthritis": [ + "HP:0040312" + ], + "arthritis of temporomandibular joint": [ + "HP:0040312" + ], + "oligoarthritis": [ + "HP:0040313" + ], + "blind vagina": [ + "HP:0040314" + ], + "blind - end vagina": [ + "HP:0040314" + ], + "blind - ended vagina": [ + "HP:0040314" + ], + "tongue edema": [ + "HP:0040315" + ], + "tongue oedema": [ + "HP:0040315" + ], + "obsolete aplasia of the penis": [ + "HP:0040316" + ], + "blue urine": [ + "HP:0040317" + ], + "red urine": [ + "HP:0040318" + ], + "dark urine": [ + "HP:0040319" + ], + "red - brown urine": [ + "HP:0040320" + ], + "red brown urine": [ + "HP:0040320" + ], + "dark yellow urine": [ + "HP:0040321" + ], + "purple urine": [ + "HP:0040322" + ], + "erythema of the eyelid": [ + "HP:0040323" + ], + "erythema of the eyelids": [ + "HP:0040323" + ], + "erythema of eyelid": [ + "HP:0040323" + ], + "eyelid erythema": [ + "HP:0040323" + ], + "heliotrope rash": [ + "HP:0040324" + ], + "heliotrope erythema": [ + "HP:0040324" + ], + "bull 's eye rash": [ + "HP:0040325" + ], + "hypoplasia of the olfactory bulb": [ + "HP:0040326" + ], + "hypoplasia of olfactory bulb": [ + "HP:0040326" + ], + "hypoplastic olfactory bulb": [ + "HP:0040326" + ], + "abnormal morphology of the olfactory bulb": [ + "HP:0040327" + ], + "focal hyperintensity of cerebral white matter on mri": [ + "HP:0040328" + ], + "multifocal hyperintensity of cerebral white matter on mri": [ + "HP:0040329" + ], + "confluent hyperintensity of cerebral white matter on mri": [ + "HP:0040330" + ], + "focal hypointensity of cerebral white matter on mri": [ + "HP:0040331" + ], + "multifocal hypointensity of cerebral white matter on mri": [ + "HP:0040332" + ], + "confluent hypointensity of cerebral white matter on mri": [ + "HP:0040333" + ], + "purulent rhinitis": [ + "HP:0040334" + ], + "absent neutrophil lactoferrin": [ + "HP:0041042" + ], + "neutrophil nuclear cleft": [ + "HP:0041043" + ], + "neutrophil nuclear clefts": [ + "HP:0041043" + ], + "low neutrophil alkaline phosphatase": [ + "HP:0041044" + ], + "increase neutrophil mitochondrion": [ + "HP:0041045" + ], + "increased neutrophil mitochondria": [ + "HP:0041045" + ], + "increase neutrophil ribosome": [ + "HP:0041046" + ], + "increased neutrophil ribosomes": [ + "HP:0041046" + ], + "bladder outlet obstruction": [ + "HP:0041047" + ], + "obstruction of bladder outlet": [ + "HP:0041047" + ], + "decreased expression of gpi - anchored protein on the cell surface": [ + "HP:0041048" + ], + "decreased expression of gpi - anchored proteins on the cell surface": [ + "HP:0041048" + ], + "starch intolerance": [ + "HP:0041049" + ], + "amylose - amylopectin intolerance": [ + "HP:0041049" + ], + "renal tubular cyst": [ + "HP:0041050" + ], + "renal tubule cyst": [ + "HP:0041050" + ], + "ageusia": [ + "HP:0041051" + ], + "absent sense of taste": [ + "HP:0041051" + ], + "impaired taste sensation": [ + "HP:0041051" + ], + "lose taste": [ + "HP:0041051" + ], + "lost taste": [ + "HP:0041051" + ], + "agenesis of putamen": [ + "HP:0041052" + ], + "fracture head": [ + "HP:0041053" + ], + "fractured head": [ + "HP:0041053" + ], + "bone head": [ + "HP:0041053" + ], + "obsolete fracture thoracic segment of trunk": [ + "HP:0041054" + ], + "obsolete fractured thoracic segment of trunk": [ + "HP:0041054" + ], + "fracture humerus": [ + "HP:0041055" + ], + "fractured humerus": [ + "HP:0041055" + ], + "bone humerus": [ + "HP:0041055" + ], + "break humerus": [ + "HP:0041055" + ], + "broken humerus": [ + "HP:0041055" + ], + "fracture of the humerus": [ + "HP:0041055" + ], + "humeral fracture": [ + "HP:0041055" + ], + "humerus fracture": [ + "HP:0041055" + ], + "hot cross bun sign": [ + "HP:0041056" + ], + "transient decrease circulate igg4": [ + "HP:0041057" + ], + "transient decreased circulating igg4": [ + "HP:0041057" + ], + "transient decrease igg4 in blood": [ + "HP:0041057" + ], + "transient decreased igg4 in blood": [ + "HP:0041057" + ], + "chronic decrease circulate igg4": [ + "HP:0041058" + ], + "chronic decreased circulating igg4": [ + "HP:0041058" + ], + "chronic decrease igg4 in blood": [ + "HP:0041058" + ], + "chronic decreased igg4 in blood": [ + "HP:0041058" + ], + "chronic ( near ) absent circulate igg4": [ + "HP:0041059" + ], + "chronic ( near ) absent circulating igg4": [ + "HP:0041059" + ], + "chronic ( near ) absent igg4 in blood": [ + "HP:0041059" + ], + "chronic partially decrease circulating igg4": [ + "HP:0041060" + ], + "chronic partially decreased circulating igg4": [ + "HP:0041060" + ], + "chronic partially decrease igg4 in blood": [ + "HP:0041060" + ], + "chronic partially decreased igg4 in blood": [ + "HP:0041060" + ], + "fracture calcaneus": [ + "HP:0041061" + ], + "fractured calcaneus": [ + "HP:0041061" + ], + "bone calcaneus": [ + "HP:0041061" + ], + "transient decrease circulate igg2": [ + "HP:0041062" + ], + "transient decreased circulating igg2": [ + "HP:0041062" + ], + "transient decrease igg2 in blood": [ + "HP:0041062" + ], + "transient decreased igg2 in blood": [ + "HP:0041062" + ], + "chronic decrease cirulating igg2": [ + "HP:0041063" + ], + "chronic decreased cirulating igg2": [ + "HP:0041063" + ], + "chronic decrease igg2 in blood": [ + "HP:0041063" + ], + "chronic decreased igg2 in blood": [ + "HP:0041063" + ], + "fracture knee": [ + "HP:0041064" + ], + "fractured knee": [ + "HP:0041064" + ], + "bone knee": [ + "HP:0041064" + ], + "chronic ( near ) absent circulate igg2": [ + "HP:0041065" + ], + "chronic ( near ) absent circulating igg2": [ + "HP:0041065" + ], + "chronic ( near ) absent igg2 in blood": [ + "HP:0041065" + ], + "chronic partially decrease circulating igg2": [ + "HP:0041066" + ], + "chronic partially decreased circulating igg2": [ + "HP:0041066" + ], + "chronic partially decrease igg2 in blood": [ + "HP:0041066" + ], + "chronic partially decreased igg2 in blood": [ + "HP:0041066" + ], + "transient decrease circulate igg1": [ + "HP:0041067" + ], + "transient decreased circulating igg1": [ + "HP:0041067" + ], + "transient decrease igg1 in blood": [ + "HP:0041067" + ], + "transient decreased igg1 in blood": [ + "HP:0041067" + ], + "chronic decrease circulate igg1": [ + "HP:0041068" + ], + "chronic decreased circulating igg1": [ + "HP:0041068" + ], + "chronic decrease igg1 in blood": [ + "HP:0041068" + ], + "chronic decreased igg1 in blood": [ + "HP:0041068" + ], + "chronic ( near ) absent circulate igg1": [ + "HP:0041069" + ], + "chronic ( near ) absent circulating igg1": [ + "HP:0041069" + ], + "chronic ( near ) absent igg1 in blood": [ + "HP:0041069" + ], + "chronic partially decrease circulating igg1": [ + "HP:0041070" + ], + "chronic partially decreased circulating igg1": [ + "HP:0041070" + ], + "chronic partially decrease igg1 in blood": [ + "HP:0041070" + ], + "chronic partially decreased igg1 in blood": [ + "HP:0041070" + ], + "transient decrease circulate igg3": [ + "HP:0041071" + ], + "transient decreased circulating igg3": [ + "HP:0041071" + ], + "transient decrease igg3 in blood": [ + "HP:0041071" + ], + "transient decreased igg3 in blood": [ + "HP:0041071" + ], + "chronic decrease circulate igg3": [ + "HP:0041072" + ], + "chronic decreased circulating igg3": [ + "HP:0041072" + ], + "chronic decrease igg3 in blood": [ + "HP:0041072" + ], + "chronic decreased igg3 in blood": [ + "HP:0041072" + ], + "fracture thoracic vertebra": [ + "HP:0041073" + ], + "fractured thoracic vertebra": [ + "HP:0041073" + ], + "bone thoracic vertebra": [ + "HP:0041073" + ], + "chronic ( near ) absent circulate igg3": [ + "HP:0041074" + ], + "chronic ( near ) absent circulating igg3": [ + "HP:0041074" + ], + "chronic ( near ) absent igg3 in blood": [ + "HP:0041074" + ], + "chronic partially decrease circulating igg3": [ + "HP:0041075" + ], + "chronic partially decreased circulating igg3": [ + "HP:0041075" + ], + "chronic partially decrease igg3 in blood": [ + "HP:0041075" + ], + "chronic partially decreased igg3 in blood": [ + "HP:0041075" + ], + "abnormal immunoglobulin level in body fluid": [ + "HP:0041076" + ], + "increase immunoglobulin level in body fluid": [ + "HP:0041077" + ], + "increased immunoglobulin level in body fluid": [ + "HP:0041077" + ], + "decrease immunoglobulin level in body fluid": [ + "HP:0041078" + ], + "decreased immunoglobulin level in body fluid": [ + "HP:0041078" + ], + "decrease body fat percentage": [ + "HP:0041079" + ], + "decreased body fat percentage": [ + "HP:0041079" + ], + "decrease adipose tissue percentage": [ + "HP:0041079" + ], + "decreased adipose tissue percentage": [ + "HP:0041079" + ], + "abnormal proportion of exhausted t cell": [ + "HP:0041080" + ], + "abnormal proportion of exhausted t cells": [ + "HP:0041080" + ], + "fracture low leg": [ + "HP:0041081" + ], + "fractured lower leg": [ + "HP:0041081" + ], + "fracture of the low leg": [ + "HP:0041081" + ], + "fracture of the lower leg": [ + "HP:0041081" + ], + "low extremity fracture": [ + "HP:0041081" + ], + "lower extremity fracture": [ + "HP:0041081" + ], + "low limb fracture": [ + "HP:0041081" + ], + "lower limb fracture": [ + "HP:0041081" + ], + "fracture skull": [ + "HP:0041082" + ], + "fractured skull": [ + "HP:0041082" + ], + "bone skull": [ + "HP:0041082" + ], + "fracture phalanx": [ + "HP:0041083" + ], + "fractured phalanx": [ + "HP:0041083" + ], + "bone phalanx": [ + "HP:0041083" + ], + "compression - fracture thoracic vertebra": [ + "HP:0041084" + ], + "compression - fractured thoracic vertebra": [ + "HP:0041084" + ], + "compression fracture thoracic vertebra": [ + "HP:0041084" + ], + "compression fractured thoracic vertebra": [ + "HP:0041084" + ], + "wedge fracture thoracic vertebra": [ + "HP:0041084" + ], + "wedge fractured thoracic vertebra": [ + "HP:0041084" + ], + "compression - fracture vertebra": [ + "HP:0041085" + ], + "compression - fractured vertebra": [ + "HP:0041085" + ], + "compression fracture vertebra": [ + "HP:0041085" + ], + "compression fractured vertebra": [ + "HP:0041085" + ], + "wedge fracture vertebra": [ + "HP:0041085" + ], + "wedge fractured vertebra": [ + "HP:0041085" + ], + "compression - fractured cervical vertebra": [ + "HP:0041086" + ], + "compression fracture cervical vertebra": [ + "HP:0041086" + ], + "compression fractured cervical vertebra": [ + "HP:0041086" + ], + "wedge fracture cervical vertebra": [ + "HP:0041086" + ], + "wedge fractured cervical vertebra": [ + "HP:0041086" + ], + "compression - fracture lumbar vertebra": [ + "HP:0041087" + ], + "compression - fractured lumbar vertebra": [ + "HP:0041087" + ], + "compression fracture lumbar vertebra": [ + "HP:0041087" + ], + "compression fractured lumbar vertebra": [ + "HP:0041087" + ], + "wedge fracture lumbar vertebra": [ + "HP:0041087" + ], + "wedge fractured lumbar vertebra": [ + "HP:0041087" + ], + "avulsion fracture humerus": [ + "HP:0041088" + ], + "avulsion fractured humerus": [ + "HP:0041088" + ], + "avulsion fracture tibia": [ + "HP:0041089" + ], + "avulsion fractured tibia": [ + "HP:0041089" + ], + "obsolete avulsion fracture pelvic region of trunk": [ + "HP:0041090" + ], + "obsolete avulsion fractured pelvic region of trunk": [ + "HP:0041090" + ], + "avulsion fracture epiphysis of femur": [ + "HP:0041091" + ], + "avulsion fractured epiphysis of femur": [ + "HP:0041091" + ], + "emotional hypersensitivity": [ + "HP:0041092" + ], + "highly sensitive": [ + "HP:0041092" + ], + "hypersensitivity": [ + "HP:0041092" + ], + "overly sensitive": [ + "HP:0041092" + ], + "beau 's line": [ + "HP:0041093" + ], + "beau 's lines": [ + "HP:0041093" + ], + "beau line": [ + "HP:0041093" + ], + "beau lines": [ + "HP:0041093" + ], + "ladder nail": [ + "HP:0041093" + ], + "ladder nail sign": [ + "HP:0041093" + ], + "complete tracheal ring": [ + "HP:0041094" + ], + "complete tracheal ring deformity": [ + "HP:0041094" + ], + "complete tracheal rings": [ + "HP:0041094" + ], + "fractured metaphysis of femur": [ + "HP:0041114" + ], + "bone metaphysis of femur": [ + "HP:0041114" + ], + "fracture right clavicle": [ + "HP:0041115" + ], + "fractured right clavicle": [ + "HP:0041115" + ], + "bone right clavicle": [ + "HP:0041115" + ], + "fracture leave clavicle": [ + "HP:0041116" + ], + "fractured left clavicle": [ + "HP:0041116" + ], + "bone leave clavicle": [ + "HP:0041116" + ], + "bone left clavicle": [ + "HP:0041116" + ], + "fracture low limb segment": [ + "HP:0041117" + ], + "fractured lower limb segment": [ + "HP:0041117" + ], + "bone low limb segment": [ + "HP:0041117" + ], + "bone lower limb segment": [ + "HP:0041117" + ], + "fracture upper limb segment": [ + "HP:0041118" + ], + "fractured upper limb segment": [ + "HP:0041118" + ], + "bone upper limb segment": [ + "HP:0041118" + ], + "fracture metacarpus skeleton": [ + "HP:0041119" + ], + "fractured metacarpus skeleton": [ + "HP:0041119" + ], + "bone metacarpus skeleton": [ + "HP:0041119" + ], + "fractured epiphysis of fifth metacarpal bone": [ + "HP:0041121" + ], + "bone epiphysis of fifth metacarpal bone": [ + "HP:0041121" + ], + "fracture tibia": [ + "HP:0041143" + ], + "fractured tibia": [ + "HP:0041143" + ], + "bone tibia": [ + "HP:0041143" + ], + "break tibia": [ + "HP:0041143" + ], + "broken tibia": [ + "HP:0041143" + ], + "fracture of the tibia": [ + "HP:0041143" + ], + "tibial fracture": [ + "HP:0041143" + ], + "fracture clavicle bone": [ + "HP:0041144" + ], + "fractured clavicle bone": [ + "HP:0041144" + ], + "bone clavicle bone": [ + "HP:0041144" + ], + "fracture acetabular part of hip bone": [ + "HP:0041145" + ], + "fractured acetabular part of hip bone": [ + "HP:0041145" + ], + "bone acetabular part of hip bone": [ + "HP:0041145" + ], + "fracture coccyx": [ + "HP:0041146" + ], + "fractured coccyx": [ + "HP:0041146" + ], + "bone coccyx": [ + "HP:0041146" + ], + "fracture epiphysis": [ + "HP:0041147" + ], + "fractured epiphysis": [ + "HP:0041147" + ], + "bone epiphysis": [ + "HP:0041147" + ], + "fracture navicular bone of pe": [ + "HP:0041149" + ], + "fractured navicular bone of pes": [ + "HP:0041149" + ], + "bone navicular bone of pe": [ + "HP:0041149" + ], + "bone navicular bone of pes": [ + "HP:0041149" + ], + "fracture cuboid bone": [ + "HP:0041150" + ], + "fractured cuboid bone": [ + "HP:0041150" + ], + "bone cuboid bone": [ + "HP:0041150" + ], + "fracture sternoclavicular joint": [ + "HP:0041152" + ], + "fractured sternoclavicular joint": [ + "HP:0041152" + ], + "bone sternoclavicular joint": [ + "HP:0041152" + ], + "fracture ankle": [ + "HP:0041153" + ], + "fractured ankle": [ + "HP:0041153" + ], + "bone ankle joint": [ + "HP:0041153" + ], + "fracture elbow joint": [ + "HP:0041154" + ], + "fractured elbow joint": [ + "HP:0041154" + ], + "bone elbow joint": [ + "HP:0041154" + ], + "fracture mandible": [ + "HP:0041155" + ], + "fractured mandible": [ + "HP:0041155" + ], + "bone mandible": [ + "HP:0041155" + ], + "fractured orbit of skull": [ + "HP:0041156" + ], + "bone orbit of skull": [ + "HP:0041156" + ], + "fracture larynx": [ + "HP:0041157" + ], + "fractured larynx": [ + "HP:0041157" + ], + "bone larynx": [ + "HP:0041157" + ], + "obsolete fracture trunk": [ + "HP:0041158" + ], + "obsolete fractured trunk": [ + "HP:0041158" + ], + "fracture rib": [ + "HP:0041159" + ], + "fractured rib": [ + "HP:0041159" + ], + "bone rib": [ + "HP:0041159" + ], + "obsolete fracture pelvic region of trunk": [ + "HP:0041161" + ], + "obsolete fractured pelvic region of trunk": [ + "HP:0041161" + ], + "fractured foot bone": [ + "HP:0041162" + ], + "bone pe": [ + "HP:0041162" + ], + "bone pes": [ + "HP:0041162" + ], + "broken foot": [ + "HP:0041162" + ], + "fracture pe": [ + "HP:0041162" + ], + "fractured pes": [ + "HP:0041162" + ], + "metatarsal fracture": [ + "HP:0041162" + ], + "fracture manual digit": [ + "HP:0041163" + ], + "fractured manual digit": [ + "HP:0041163" + ], + "bone manual digit": [ + "HP:0041163" + ], + "fracture talus": [ + "HP:0041164" + ], + "fractured talus": [ + "HP:0041164" + ], + "bone talus": [ + "HP:0041164" + ], + "fracture maxilla": [ + "HP:0041165" + ], + "fractured maxilla": [ + "HP:0041165" + ], + "bone maxilla": [ + "HP:0041165" + ], + "fracture vertebra": [ + "HP:0041166" + ], + "fractured vertebra": [ + "HP:0041166" + ], + "bone vertebra": [ + "HP:0041166" + ], + "fractured cervical vertebra": [ + "HP:0041167" + ], + "bone cervical vertebra": [ + "HP:0041167" + ], + "fracture lumbar vertebra": [ + "HP:0041168" + ], + "fractured lumbar vertebra": [ + "HP:0041168" + ], + "bone lumbar vertebra": [ + "HP:0041168" + ], + "fracture fuse sacrum": [ + "HP:0041172" + ], + "fractured fused sacrum": [ + "HP:0041172" + ], + "bone fuse sacrum": [ + "HP:0041172" + ], + "bone fused sacrum": [ + "HP:0041172" + ], + "fracture metacarpophalangeal joint": [ + "HP:0041173" + ], + "fractured metacarpophalangeal joint": [ + "HP:0041173" + ], + "bone metacarpophalangeal joint": [ + "HP:0041173" + ], + "fracture distal phalanx of manus": [ + "HP:0041174" + ], + "fractured distal phalanx of manus": [ + "HP:0041174" + ], + "bone distal phalanx of manus": [ + "HP:0041174" + ], + "fracture middle phalanx of pe": [ + "HP:0041175" + ], + "fractured middle phalanx of pes": [ + "HP:0041175" + ], + "bone middle phalanx of pe": [ + "HP:0041175" + ], + "bone middle phalanx of pes": [ + "HP:0041175" + ], + "fracture distal phalanx of manual digit 2": [ + "HP:0041176" + ], + "fractured distal phalanx of manual digit 2": [ + "HP:0041176" + ], + "bone distal phalanx of manual digit 2": [ + "HP:0041176" + ], + "fracture distal phalanx of manual digit 3": [ + "HP:0041177" + ], + "fractured distal phalanx of manual digit 3": [ + "HP:0041177" + ], + "bone distal phalanx of manual 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phalanx of manual digit 2": [ + "HP:0041182" + ], + "fracture middle phalanx of manual digit 3": [ + "HP:0041183" + ], + "fractured middle phalanx of manual digit 3": [ + "HP:0041183" + ], + "bone middle phalanx of manual digit 3": [ + "HP:0041183" + ], + "fracture middle phalanx of manual digit 4": [ + "HP:0041184" + ], + "fractured middle phalanx of manual digit 4": [ + "HP:0041184" + ], + "bone middle phalanx of manual digit 4": [ + "HP:0041184" + ], + "fracture middle phalanx of manual digit 5": [ + "HP:0041185" + ], + "fractured middle phalanx of manual digit 5": [ + "HP:0041185" + ], + "bone middle phalanx of manual digit 5": [ + "HP:0041185" + ], + "fracture middle phalanx of pedal digit 3": [ + "HP:0041186" + ], + "fractured middle phalanx of pedal digit 3": [ + "HP:0041186" + ], + "bone middle phalanx of pedal digit 3": [ + "HP:0041186" + ], + "fracture proximal phalanx of pedal digit 1": [ + "HP:0041187" + ], + "fractured proximal phalanx of pedal digit 1": [ + "HP:0041187" + ], + "bone proximal phalanx of pedal digit 1": [ + "HP:0041187" + ], + "fracture proximal phalanx of manual digit 1": [ + "HP:0041188" + ], + "fractured proximal phalanx of manual digit 1": [ + "HP:0041188" + ], + "bone proximal phalanx of manual digit 1": [ + "HP:0041188" + ], + "fractured epiphysis of femur": [ + "HP:0041189" + ], + "bone epiphysis of femur": [ + "HP:0041189" + ], + "fractured epiphysis of second metacarpal bone": [ + "HP:0041190" + ], + "bone epiphysis of second metacarpal bone": [ + "HP:0041190" + ], + "fractured epiphysis of third metacarpal bone": [ + "HP:0041191" + ], + "bone epiphysis of third metacarpal bone": [ + "HP:0041191" + ], + "fractured epiphysis of fourth metacarpal bone": [ + "HP:0041192" + ], + "bone epiphysis of fourth metacarpal bone": [ + "HP:0041192" + ], + "fractured epiphysis of first metatarsal bone": [ + "HP:0041193" + ], + "bone epiphysis of first metatarsal bone": [ + "HP:0041193" + ], + "fractured epiphysis of second metatarsal bone": [ + "HP:0041194" + ], + "bone epiphysis of second metatarsal bone": [ + "HP:0041194" + ], + "fractured epiphysis of third metatarsal bone": [ + "HP:0041195" + ], + "bone epiphysis of third metatarsal bone": [ + "HP:0041195" + ], + "fracture distal epiphysis of radius": [ + "HP:0041196" + ], + "fractured distal epiphysis of radius": [ + "HP:0041196" + ], + "bone distal epiphysis of radius": [ + "HP:0041196" + ], + "fracture proximal epiphysis of first metacarpal bone": [ + "HP:0041197" + ], + "fractured proximal epiphysis of first metacarpal bone": [ + "HP:0041197" + ], + "bone proximal epiphysis of first metacarpal bone": [ + "HP:0041197" + ], + "fracture proximal epiphysis of middle phalanx of manual digit 3": [ + "HP:0041198" + ], + "fractured proximal epiphysis of middle phalanx of manual digit 3": [ + "HP:0041198" + ], + "bone proximal epiphysis of middle phalanx of manual digit 3": [ + "HP:0041198" + ], + "fracture interphalangeal joint": [ + "HP:0041199" + ], + "fractured interphalangeal joint": [ + "HP:0041199" + ], + "bone interphalangeal joint": [ + "HP:0041199" + ], + "fracture sternal end of clavicle": [ + "HP:0041200" + ], + "fractured sternal end of clavicle": [ + "HP:0041200" + ], + "bone sternal end of clavicle": [ + "HP:0041200" + ], + "fractured epiphysis of middle phalanx of manus": [ + "HP:0041209" + ], + "bone epiphysis of middle phalanx of manus": [ + "HP:0041209" + ], + "fractured lateral malleolus of fibula": [ + "HP:0041210" + ], + "bone lateral malleolus of fibula": [ + "HP:0041210" + ], + "fracture proximal phalanx of digit 2": [ + "HP:0041211" + ], + "fractured proximal phalanx of digit 2": [ + "HP:0041211" + ], + "bone proximal phalanx of digit 2": [ + "HP:0041211" + ], + "fracture proximal phalanx of digit 3": [ + "HP:0041212" + ], + "fractured proximal phalanx of digit 3": [ + "HP:0041212" + ], + "bone proximal phalanx of digit 3": [ + "HP:0041212" + ], + "fracture proximal phalanx of digit 4": [ + "HP:0041213" + ], + "fractured proximal phalanx of digit 4": [ + "HP:0041213" + ], + "bone proximal phalanx of digit 4": [ + "HP:0041213" + ], + "fracture proximal phalanx of digit 5": [ + "HP:0041214" + ], + "fractured proximal phalanx of digit 5": [ + "HP:0041214" + ], + "bone proximal phalanx of digit 5": [ + "HP:0041214" + ], + "fracture fuse metatarsal bone 2 - 4": [ + "HP:0041215" + ], + "fractured fused metatarsal bones 2 - 4": [ + "HP:0041215" + ], + "bone fuse metatarsal bone 2 - 4": [ + "HP:0041215" + ], + "bone fused metatarsal bones 2 - 4": [ + "HP:0041215" + ], + "fracture distal epiphysis of distal phalanx of manual digit 1": [ + "HP:0041216" + ], + "fractured distal epiphysis of distal phalanx of manual digit 1": [ + "HP:0041216" + ], + "bone distal epiphysis of distal phalanx of manual digit 1": [ + "HP:0041216" + ], + "fracture shoulder": [ + "HP:0041217" + ], + "fractured shoulder": [ + "HP:0041217" + ], + "bone shoulder joint": [ + "HP:0041217" + ], + "fracture distal phalanx": [ + "HP:0041218" + ], + "fractured distal phalanx": [ + "HP:0041218" + ], + "bone distal phalanx": [ + "HP:0041218" + ], + "fracture elbow": [ + "HP:0041219" + ], + "fractured elbow": [ + "HP:0041219" + ], + "bone elbow": [ + "HP:0041219" + ], + "fracture facial bone": [ + "HP:0041220" + ], + "fractured facial bone": [ + "HP:0041220" + ], + "bone facial bone": [ + "HP:0041220" + ], + "fracture head of femur": [ + "HP:0041221" + ], + "fractured head of femur": [ + "HP:0041221" + ], + "bone head of femur": [ + "HP:0041221" + ], + "fracture fibula": [ + "HP:0041222" + ], + "fractured fibula": [ + "HP:0041222" + ], + "bone fibula": [ + "HP:0041222" + ], + "break fibula": [ + "HP:0041222" + ], + "broken fibula": [ + "HP:0041222" + ], + "fibula fracture": [ + "HP:0041222" + ], + "fracture of the fibula": [ + "HP:0041222" + ], + "fracture metatarsal bone of digit 5": [ + "HP:0041223" + ], + "fractured metatarsal bone of digit 5": [ + "HP:0041223" + ], + "bone metatarsal bone of digit 5": [ + "HP:0041223" + ], + "fracture manual digit bone": [ + "HP:0041224" + ], + "fractured manual digit bone": [ + "HP:0041224" + ], + "bone manual digit bone": [ + "HP:0041224" + ], + "fracture metacarpal bone of digit 1": [ + "HP:0041225" + ], + "fractured metacarpal bone of digit 1": [ + "HP:0041225" + ], + "bone metacarpal bone of digit 1": [ + "HP:0041225" + ], + "fracture distal tarsal bone": [ + "HP:0041226" + ], + "fractured distal tarsal bone": [ + "HP:0041226" + ], + "bone distal tarsal bone": [ + "HP:0041226" + ], + "fracture distal tarsal bone 2": [ + "HP:0041227" + ], + "fractured distal tarsal bone 2": [ + "HP:0041227" + ], + "bone distal tarsal bone 2": [ + "HP:0041227" + ], + "fracture distal tarsal bone 3": [ + "HP:0041228" + ], + "fractured distal tarsal bone 3": [ + "HP:0041228" + ], + "bone distal tarsal bone 3": [ + "HP:0041228" + ], + "fracture metatarsal bone of digit 4": [ + "HP:0041230" + ], + "fractured metatarsal bone of digit 4": [ + "HP:0041230" + ], + "bone metatarsal bone of digit 4": [ + "HP:0041230" + ], + "fracture metatarsal bone of digit 1": [ + "HP:0041231" + ], + "fractured metatarsal bone of digit 1": [ + "HP:0041231" + ], + "bone metatarsal bone of digit 1": [ + "HP:0041231" + ], + "fracture skeleton of manual acropodium": [ + "HP:0041232" + ], + "fractured skeleton of manual acropodium": [ + "HP:0041232" + ], + "bone skeleton of manual acropodium": [ + "HP:0041232" + ], + "fractured ilium": [ + "HP:0041233" + ], + "bone ilium": [ + "HP:0041233" + ], + "fracture bone of jaw": [ + "HP:0041234" + ], + "fractured bone of jaw": [ + "HP:0041234" + ], + "bone bone of jaw": [ + "HP:0041234" + ], + "fracture hindlimb bone": [ + "HP:0041235" + ], + "fractured hindlimb bone": [ + "HP:0041235" + ], + "bone hindlimb bone": [ + "HP:0041235" + ], + "fracture middle phalanx of manus": [ + "HP:0041236" + ], + "fractured middle phalanx of manus": [ + "HP:0041236" + ], + "bone middle phalanx of manus": [ + "HP:0041236" + ], + "fracture patella": [ + "HP:0041237" + ], + "fractured patella": [ + "HP:0041237" + ], + "bone patella": [ + "HP:0041237" + ], + "fracture manual digit 1 phalanx": [ + "HP:0041239" + ], + "fractured manual digit 1 phalanx": [ + "HP:0041239" + ], + "bone manual digit 1 phalanx": [ + "HP:0041239" + ], + "fracture phalanx of pe": [ + "HP:0041240" + ], + "fractured phalanx of pes": [ + "HP:0041240" + ], + "bone phalanx of pe": [ + "HP:0041240" + ], + "bone phalanx of pes": [ + "HP:0041240" + ], + "fracture phalanx of manus": [ + "HP:0041241" + ], + "fractured phalanx of manus": [ + "HP:0041241" + ], + "bone phalanx of manus": [ + "HP:0041241" + ], + "fracture proximal phalanx of manus": [ + "HP:0041243" + ], + "fractured proximal phalanx of manus": [ + "HP:0041243" + ], + "bone proximal phalanx of manus": [ + "HP:0041243" + ], + "fracture scapula": [ + "HP:0041244" + ], + "fractured scapula": [ + "HP:0041244" + ], + "bone scapula": [ + "HP:0041244" + ], + "fracture shoulder bone": [ + "HP:0041245" + ], + "fractured shoulder bone": [ + "HP:0041245" + ], + "bone shoulder bone": [ + "HP:0041245" + ], + "fracture sternum": [ + "HP:0041246" + ], + "fractured sternum": [ + "HP:0041246" + ], + "bone sternum": [ + "HP:0041246" + ], + "fracture tarsal bone": [ + "HP:0041247" + ], + "fractured tarsal bone": [ + "HP:0041247" + ], + "bone tarsal bone": [ + "HP:0041247" + ], + "fracture carpal bone": [ + "HP:0041248" + ], + "fractured carpal bone": [ + "HP:0041248" + ], + "bone carpal bone": [ + "HP:0041248" + ], + "broken wrist": [ + "HP:0041248" + ], + "carpal bone fracture": [ + "HP:0041248" + ], + "fracture wrist": [ + "HP:0041248" + ], + "fractured wrist": [ + "HP:0041248" + ], + "wrist fracture": [ + "HP:0041248" + ], + "fracture nose": [ + "HP:0041249" + ], + "fractured nose": [ + "HP:0041249" + ], + "bone nose": [ + "HP:0041249" + ], + "abnormal ossification of the trapezium": [ + "HP:0045001" + ], + "absent ossification of the trapezium": [ + "HP:0045002" + ], + "abnormal ossification of the scaphoid": [ + "HP:0045003" + ], + "abnormal ossification of the trapezoid bone": [ + "HP:0045004" + ], + "neural tube defect": [ + "HP:0045005" + ], + "abnormality of neural tube closure": [ + "HP:0045005" + ], + "aplasia of lymphatic vessel": [ + "HP:0045006" + ], + "aplasia of lymphatic vessels": [ + "HP:0045006" + ], + "absent lymphatic vessel": [ + "HP:0045006" + ], + "absent lymphatic vessels": [ + "HP:0045006" + ], + "abnormal substantia nigra morphology": [ + "HP:0045007" + ], + "abnormality of the substantia nigra": [ + "HP:0045007" + ], + "abnormal shape of the radius": [ + "HP:0045008" + ], + "abnormal morphology of the radius": [ + "HP:0045009" + ], + "abnormality of peripheral nerve": [ + "HP:0045010" + ], + "abnormality of peripheral nerves": [ + "HP:0045010" + ], + "decrease urine bicarbonate concentration": [ + "HP:0045011" + ], + "decreased urine bicarbonate concentration": [ + "HP:0045011" + ], + "decrease urine hco3 concentration": [ + "HP:0045011" + ], + "decreased urine hco3 concentration": [ + "HP:0045011" + ], + "decrease urinary catecholamine concentration": [ + "HP:0045012" + ], + "decreased urinary catecholamine concentration": [ + "HP:0045012" + ], + "obsolete decrease urinary glucose concentration": [ + "HP:0045013" + ], + "obsolete decreased urinary glucose concentration": [ + "HP:0045013" + ], + "hypolipidemia": [ + "HP:0045014" + ], + "obsolete elevate serum long - chain fatty acid": [ + "HP:0045016" + ], + "obsolete elevated serum long - chain fatty acids": [ + "HP:0045016" + ], + "congenital malformation of the left heart": [ + "HP:0045017" + ], + "partial duplication of eyebrow": [ + "HP:0045018" + ], + "partial duplication of eyebrows": [ + "HP:0045018" + ], + "partial double eyebrow": [ + "HP:0045018" + ], + "narrow palpebral fissure": [ + "HP:0045025" + ], + "decreased size of palpebral fissure": [ + "HP:0045025" + ], + "narrow eyelid opening": [ + "HP:0045025" + ], + "narrow palpebral fissures": [ + "HP:0045025" + ], + "small opening between the eyelid": [ + "HP:0045025" + ], + "small opening between the eyelids": [ + "HP:0045025" + ], + "small palpebral fissure": [ + "HP:0045025" + ], + "small palpebral fissures": [ + "HP:0045025" + ], + "abnormality of the mediastinum": [ + "HP:0045026" + ], + "abnormality of the thoracic cavity": [ + "HP:0045027" + ], + "microlissencephaly": [ + "HP:0045028" + ], + "lissencephaly type iii": [ + "HP:0045028" + ], + "type 3 lissencephaly": [ + "HP:0045028" + ], + "type iii lissencephaly": [ + "HP:0045028" + ], + "eosinophilic fasciitis": [ + "HP:0045029" + ], + "elevate urinary aminoisobutyric acid": [ + "HP:0045034" + ], + "elevated urinary aminoisobutyric acid": [ + "HP:0045034" + ], + "decrease urinary copper concentration": [ + "HP:0045035" + ], + "decreased urinary copper concentration": [ + "HP:0045035" + ], + "abnormal urinary copper concentration": [ + "HP:0045036" + ], + "abnormality of jaw muscle": [ + "HP:0045037" + ], + "abnormality of jaw muscles": [ + "HP:0045037" + ], + "gastric lymphoma": [ + "HP:0045038" + ], + "primary gastric lymphoma": [ + "HP:0045038" + ], + "osteolysis involve bone of the upper limb": [ + "HP:0045039" + ], + "osteolysis involving bones of the upper limbs": [ + "HP:0045039" + ], + "abnormal lactate dehydrogenase level": [ + "HP:0045040" + ], + "reduce lactate dehydrogenase b level": [ + "HP:0045041" + ], + "reduced lactate dehydrogenase b level": [ + "HP:0045041" + ], + "decrease serum complement c4": [ + "HP:0045042" + ], + "decreased serum complement c4": [ + "HP:0045042" + ], + "decrease serum complement c4 level": [ + "HP:0045042" + ], + "decreased serum complement c4 level": [ + "HP:0045042" + ], + "decrease serum complement c4a": [ + "HP:0045043" + ], + "decreased serum complement c4a": [ + "HP:0045043" + ], + "c4a deficiency": [ + "HP:0045043" + ], + "complement component 4a deficiency": [ + "HP:0045043" + ], + "decrease serum complement c4b": [ + "HP:0045044" + ], + "decreased serum complement c4b": [ + "HP:0045044" + ], + "c4b deficiency": [ + "HP:0045044" + ], + "complement component 4b deficiency": [ + "HP:0045044" + ], + "elevate circulate acylcarnitine concentration": [ + "HP:0045045" + ], + "elevated circulating acylcarnitine concentration": [ + "HP:0045045" + ], + "elevate plasma acylcarnitine level": [ + "HP:0045045" + ], + "elevated plasma acylcarnitine levels": [ + "HP:0045045" + ], + "reduced insulin like growth factor bind protein acid labile subunit level": [ + "HP:0045046" + ], + "reduced insulin like growth factor binding protein acid labile subunit level": [ + "HP:0045046" + ], + "acid - labile subunit deficiency": [ + "HP:0045046" + ], + "decreased level of acid labile subunit": [ + "HP:0045046" + ], + "decreased levels of acid labile subunit": [ + "HP:0045046" + ], + "hb hemoglobin": [ + "HP:0045047" + ], + "hbs hemoglobin": [ + "HP:0045047" + ], + "hb haemoglobin": [ + "HP:0045047" + ], + "hbs haemoglobin": [ + "HP:0045047" + ], + "increase hba2 hemoglobin": [ + "HP:0045048" + ], + "increased hba2 hemoglobin": [ + "HP:0045048" + ], + "increase haemoglobin a2": [ + "HP:0045048" + ], + "increased haemoglobin a2": [ + "HP:0045048" + ], + "increase hba2 haemoglobin": [ + "HP:0045048" + ], + "increased hba2 haemoglobin": [ + "HP:0045048" + ], + "increase hemoglobin a2": [ + "HP:0045048" + ], + "increased hemoglobin a2": [ + "HP:0045048" + ], + "abnormal dlco": [ + "HP:0045049" + ], + "abnormal diffusing capacity": [ + "HP:0045049" + ], + "abnormal tlco": [ + "HP:0045049" + ], + "abnormal transfer factor of the lung for carbon monoxide": [ + "HP:0045049" + ], + "increase dlco": [ + "HP:0045050" + ], + "increased dlco": [ + "HP:0045050" + ], + "increase diffusing capacity": [ + "HP:0045050" + ], + "increased diffusing capacity": [ + "HP:0045050" + ], + "decrease dlco": [ + "HP:0045051" + ], + "decreased dlco": [ + "HP:0045051" + ], + "decrease diffusing capacity": [ + "HP:0045051" + ], + "decreased diffusing capacity": [ + "HP:0045051" + ], + "abnormality of the brachial nerve plexus": [ + "HP:0045052" + ], + "abnormality of the lumbosacral nerve plexus": [ + "HP:0045053" + ], + "brachial plexus neuropathy": [ + "HP:0045054" + ], + "tiger tail banding": [ + "HP:0045055" + ], + "tiger - tail banding": [ + "HP:0045055" + ], + "abnormal level of alpha - fetoprotein": [ + "HP:0045056" + ], + "abnormal levels of alpha - fetoprotein": [ + "HP:0045056" + ], + "decreased level of alpha - fetoprotein": [ + "HP:0045057" + ], + "decreased levels of alpha - fetoprotein": [ + "HP:0045057" + ], + "abnormality of the testis size": [ + "HP:0045058" + ], + "hyperkeratotic papule": [ + "HP:0045059" + ], + "aplasia / hypoplasia involve bone of the extremity": [ + "HP:0045060" + ], + "aplasia / hypoplasia involving bones of the extremities": [ + "HP:0045060" + ], + "decrease carnitine level in liver": [ + "HP:0045061" + ], + "decreased carnitine level in liver": [ + "HP:0045061" + ], + "increase pivka - ii": [ + "HP:0045063" + ], + "increased pivka - ii": [ + "HP:0045063" + ], + "increase prothrombin induce by vitamin k absence - ii": [ + "HP:0045063" + ], + "increased prothrombin induced by vitamin k absence - ii": [ + "HP:0045063" + ], + "serositis": [ + "HP:0045073" + ], + "thin eyebrow": [ + "HP:0045074" + ], + "thin eyebrows": [ + "HP:0045074" + ], + "sparse eyebrow": [ + "HP:0045075" + ], + "hypotrichosis of eyebrow": [ + "HP:0045075" + ], + "sparse eyebrows": [ + "HP:0045075" + ], + "distal femoral metaphyseal irregularity": [ + "HP:0045079" + ], + "irregular distal femoral metaphyses": [ + "HP:0045079" + ], + "decreased proportion of cd3 - positive t cell": [ + "HP:0045080" + ], + "decreased proportion of cd3 - positive t cells": [ + "HP:0045080" + ], + "decreased proportion of cd3+ t cell": [ + "HP:0045080" + ], + "decreased proportion of cd3+ t cells": [ + "HP:0045080" + ], + "abnormality of body mass index": [ + "HP:0045081" + ], + "abnormal bmi": [ + "HP:0045081" + ], + "abnormal body mass index": [ + "HP:0045081" + ], + "decrease body mass index": [ + "HP:0045082" + ], + "decreased body mass index": [ + "HP:0045082" + ], + "decrease bmi": [ + "HP:0045082" + ], + "decreased bmi": [ + "HP:0045082" + ], + "obsolete increase body mass index": [ + "HP:0045083" + ], + "obsolete increased body mass index": [ + "HP:0045083" + ], + "limb myoclonus": [ + "HP:0045084" + ], + "myoclonus of limb": [ + "HP:0045084" + ], + "myoclonus of limbs": [ + "HP:0045084" + ], + "atrophy of masseter muscle": [ + "HP:0045085" + ], + "atrophy masseter muscle": [ + "HP:0045085" + ], + "atrophied masseter muscle": [ + "HP:0045085" + ], + "masseter muscle atrophy": [ + "HP:0045085" + ], + "knee joint hypermobility": [ + "HP:0045086" + ], + "knee joint over - flexibility": [ + "HP:0045086" + ], + "hip joint hypermobility": [ + "HP:0045087" + ], + "clinical relevance": [ + "HP:0045088" + ], + "distinctive finding": [ + "HP:0045089" + ], + "minor finding": [ + "HP:0045090" + ], + "anorgasmia": [ + "HP:0046502" + ], + "increase libido": [ + "HP:0046503" + ], + "increased libido": [ + "HP:0046503" + ], + "decrease libido": [ + "HP:0046504" + ], + "decreased libido": [ + "HP:0046504" + ], + "hand pain": [ + "HP:0046505" + ], + "pain in head and neck region": [ + "HP:0046506" + ], + "bradypnea": [ + "HP:0046507" + ], + "abnormal cervical spine morphology": [ + "HP:0046508" + ], + "early onset of sexual maturation": [ + "HP:0100000" + ], + "malignant mesothelioma": [ + "HP:0100001" + ], + "pleural mesothelioma": [ + "HP:0100002" + ], + "peritoneal mesothelioma": [ + "HP:0100003" + ], + "pericardial mesothelioma": [ + "HP:0100004" + ], + "testicular mesothelioma": [ + "HP:0100005" + ], + "neoplasm of the central nervous system": [ + "HP:0100006" + ], + "neoplasia of the central nervous system": [ + "HP:0100006" + ], + "neoplasm of the cns": [ + "HP:0100006" + ], + "tumor of the central nervous system": [ + "HP:0100006" + ], + "tumors of the central nervous system": [ + "HP:0100006" + ], + "tumour of the central nervous system": [ + "HP:0100006" + ], + "tumours of the central nervous system": [ + "HP:0100006" + ], + "neoplasm of the peripheral nervous system": [ + "HP:0100007" + ], + "tumor of the peripheral nervous system": [ + "HP:0100007" + ], + "tumour of the peripheral nervous system": [ + "HP:0100007" + ], + "schwannoma": [ + "HP:0100008" + ], + "neurilemmoma": [ + "HP:0100008" + ], + "neurinoma": [ + "HP:0100008" + ], + "neurolemmoma": [ + "HP:0100008" + ], + "schwann cell tumor": [ + "HP:0100008" + ], + "schwann cell tumour": [ + "HP:0100008" + ], + "schwannomas": [ + "HP:0100008" + ], + "intracranial meningioma": [ + "HP:0100009" + ], + "spinal meningioma": [ + "HP:0100010" + ], + "scleral schwannoma": [ + "HP:0100011" + ], + "neoplasm of the eye": [ + "HP:0100012" + ], + "eye tumor": [ + "HP:0100012" + ], + "eye tumour": [ + "HP:0100012" + ], + "neoplasia of the eye": [ + "HP:0100012" + ], + "neoplasm of the breast": [ + "HP:0100013" + ], + "breast tumor": [ + "HP:0100013" + ], + "breast tumour": [ + "HP:0100013" + ], + "neoplasia of the breast": [ + "HP:0100013" + ], + "tumour of the breast": [ + "HP:0100013" + ], + "tumours of the breast": [ + "HP:0100013" + ], + "epiretinal membrane": [ + "HP:0100014" + ], + "epiretinal membranes": [ + "HP:0100014" + ], + "macular pucker": [ + "HP:0100014" + ], + "premacular fibrosis": [ + "HP:0100014" + ], + "stahl ear": [ + "HP:0100015" + ], + "additional crus": [ + "HP:0100015" + ], + "third crus": [ + "HP:0100015" + ], + "abnormality of mesentery morphology": [ + "HP:0100016" + ], + "abnormality of the mesentery": [ + "HP:0100016" + ], + "capsular cataract": [ + "HP:0100017" + ], + "nuclear cataract": [ + "HP:0100018" + ], + "yellowish cloudy center of lens": [ + "HP:0100018" + ], + "yellowish cloudy centre of lens": [ + "HP:0100018" + ], + "cortical cataract": [ + "HP:0100019" + ], + "posterior capsular cataract": [ + "HP:0100020" + ], + "cerebral palsy": [ + "HP:0100021" + ], + "cerebral paralysis": [ + "HP:0100021" + ], + "abnormality of movement": [ + "HP:0100022" + ], + "movement disorder": [ + "HP:0100022" + ], + "unusual movement": [ + "HP:0100022" + ], + "recurrent hand flap": [ + "HP:0100023" + ], + "recurrent hand flapping": [ + "HP:0100023" + ], + "conspicuously happy disposition": [ + "HP:0100024" + ], + "conspicious happy aspect": [ + "HP:0100024" + ], + "happy aspect": [ + "HP:0100024" + ], + "overfriendliness": [ + "HP:0100025" + ], + "arteriovenous malformation": [ + "HP:0100026" + ], + "recurrent pancreatitis": [ + "HP:0100027" + ], + "recur pancreas inflammation": [ + "HP:0100027" + ], + "recurring pancreas inflammation": [ + "HP:0100027" + ], + "recur pancreatitis": [ + "HP:0100027" + ], + "recurring pancreatitis": [ + "HP:0100027" + ], + "ectopic thyroid": [ + "HP:0100028" + ], + "aberrant thyroid": [ + "HP:0100028" + ], + "aberrant thyroid gland": [ + "HP:0100028" + ], + "abnormal thryoid location": [ + "HP:0100028" + ], + "ectopic thyroid gland": [ + "HP:0100028" + ], + "heteropic thyroid gland": [ + "HP:0100028" + ], + "lingual thyroid": [ + "HP:0100029" + ], + "accessory ectopic thyroid tissue": [ + "HP:0100030" + ], + "neoplasm of the thyroid gland": [ + "HP:0100031" + ], + "neoplasia of the thyroid gland": [ + "HP:0100031" + ], + "tic": [ + "HP:0100033" + ], + "tics": [ + "HP:0100033" + ], + "tic disorder": [ + "HP:0100033" + ], + "motor tic": [ + "HP:0100034" + ], + "motor tics": [ + "HP:0100034" + ], + "phonic tic": [ + "HP:0100035" + ], + "phonic tics": [ + "HP:0100035" + ], + "verbal tic": [ + "HP:0100035" + ], + "verbal tics": [ + "HP:0100035" + ], + "vocal tic": [ + "HP:0100035" + ], + "vocal tics": [ + "HP:0100035" + ], + "pseudo - fracture": [ + "HP:0100036" + ], + "pseudo - fractures": [ + "HP:0100036" + ], + "looser zone": [ + "HP:0100036" + ], + "looser zones": [ + "HP:0100036" + ], + "abnormality of the scalp hair": [ + "HP:0100037" + ], + "slow - grow scalp hair": [ + "HP:0100038" + ], + "slow - growing scalp hair": [ + "HP:0100038" + ], + "thicken cortex of bone": [ + "HP:0100039" + ], + "thickened cortex of bones": [ + "HP:0100039" + ], + "broad 2nd toe": [ + "HP:0100040" + ], + "wide 2nd toe": [ + "HP:0100040" + ], + "broad 3rd toe": [ + "HP:0100041" + ], + "wide 3rd toe": [ + "HP:0100041" + ], + "broad 4th toe": [ + "HP:0100042" + ], + "wide 4th toe": [ + "HP:0100042" + ], + "broad 5th toe": [ + "HP:0100043" + ], + "broad little toe": [ + "HP:0100043" + ], + "broad pinkie toe": [ + "HP:0100043" + ], + "broad pinky toe": [ + "HP:0100043" + ], + "absent epiphysis of the 2nd toe": [ + "HP:0100044" + ], + "absent epiphyses of the 2nd toe": [ + "HP:0100044" + ], + "absent end part of the 2nd toe bone": [ + "HP:0100044" + ], + "bracket epiphysis of the 2nd toe": [ + "HP:0100045" + ], + "bracket epiphyses of the 2nd toe": [ + "HP:0100045" + ], + "bracket shape end part of 2nd toe bone": [ + "HP:0100045" + ], + "bracket shaped end part of 2nd toe bone": [ + "HP:0100045" + ], + "cone - shaped epiphysis of the 2nd toe": [ + "HP:0100046" + ], + "cone - shaped epiphyses of the 2nd toe": [ + "HP:0100046" + ], + "cone - shaped end part of the 2nd toe bone": [ + "HP:0100046" + ], + "enlarged epiphysis of the 2nd toe": [ + "HP:0100047" + ], + "enlarged epiphyses of the 2nd toe": [ + "HP:0100047" + ], + "enlarged end part of the 2nd toe bone": [ + "HP:0100047" + ], + "fragmentation of the epiphysis of the 2nd toe": [ + "HP:0100048" + ], + "fragmentation of the epiphyses of the 2nd toe": [ + "HP:0100048" + ], + "fragmentation of the end part of the 2nd toe bone": [ + "HP:0100048" + ], + "irregular epiphysis of the 2nd toe": [ + "HP:0100049" + ], + "irregular epiphyses of the 2nd toe": [ + "HP:0100049" + ], + "irregular end part of the 2nd toe bone": [ + "HP:0100049" + ], + "ivory epiphysis of the 2nd toe": [ + "HP:0100050" + ], + "ivory epiphyses of the 2nd toe": [ + "HP:0100050" + ], + "increase bone density of end part of the 2nd toe": [ + "HP:0100050" + ], + "increased bone density of end part of the 2nd toe": [ + "HP:0100050" + ], + "pseudoepiphyses of the 2nd toe": [ + "HP:0100051" + ], + "small epiphysis of the 2nd toe": [ + "HP:0100052" + ], + "small epiphyses of the 2nd toe": [ + "HP:0100052" + ], + "small end part of the 2nd toe bone": [ + "HP:0100052" + ], + "stippling of the epiphysis of the 2nd toe": [ + "HP:0100053" + ], + "stippling of the epiphyses of the 2nd toe": [ + "HP:0100053" + ], + "speckled calcification in the end part of the 2nd toe bone": [ + "HP:0100053" + ], + "speckled calcifications in the end part of the 2nd toe bone": [ + "HP:0100053" + ], + "triangular epiphysis of the 2nd toe": [ + "HP:0100054" + ], + "triangular epiphyses of the 2nd toe": [ + "HP:0100054" + ], + "triangular end part of the 2nd toe bone": [ + "HP:0100054" + ], + "absent epiphysis of the 3rd toe": [ + "HP:0100055" + ], + "absent epiphyses of the 3rd toe": [ + "HP:0100055" + ], + "absent end part of the 3rd toe": [ + "HP:0100055" + ], + "bracket epiphysis of the 3rd toe": [ + "HP:0100056" + ], + "bracket epiphyses of the 3rd toe": [ + "HP:0100056" + ], + "bracket shape end part of 3rd toe bone": [ + "HP:0100056" + ], + "bracket shaped end part of 3rd toe bone": [ + "HP:0100056" + ], + "cone - shaped epiphysis of the 3rd toe": [ + "HP:0100057" + ], + "cone - shaped epiphyses of the 3rd toe": [ + "HP:0100057" + ], + "cone - shaped end part of the 3rd toe bone": [ + "HP:0100057" + ], + "enlarged epiphysis of the 3rd toe": [ + "HP:0100058" + ], + "enlarged epiphyses of the 3rd toe": [ + "HP:0100058" + ], + "enlarged end part of the 3rd toe bone": [ + "HP:0100058" + ], + "fragmentation of the epiphysis of the 3rd toe": [ + "HP:0100059" + ], + "fragmentation of the epiphyses of the 3rd toe": [ + "HP:0100059" + ], + "fragmentation of the end part of the 3rd toe bone": [ + "HP:0100059" + ], + "irregular epiphysis of the 3rd toe": [ + "HP:0100060" + ], + "irregular epiphyses of the 3rd toe": [ + "HP:0100060" + ], + "irregular end part of the 3rd toe bone": [ + "HP:0100060" + ], + "ivory epiphysis of the 3rd toe": [ + "HP:0100061" + ], + "ivory epiphyses of the 3rd toe": [ + "HP:0100061" + ], + "increase bone density of end part of the 3rd toe bone": [ + "HP:0100061" + ], + "increased bone density of end part of the 3rd toe bone": [ + "HP:0100061" + ], + "pseudoepiphyses of the 3rd toe": [ + "HP:0100062" + ], + "small epiphysis of the 3rd toe": [ + "HP:0100063" + ], + "small epiphyses of the 3rd toe": [ + "HP:0100063" + ], + "small end part of the 3rd toe bone": [ + "HP:0100063" + ], + "stippling of the epiphysis of the 3rd toe": [ + "HP:0100064" + ], + "stippling of the epiphyses of the 3rd toe": [ + "HP:0100064" + ], + "speckled calcification in the end part of the 3rd toe bone": [ + "HP:0100064" + ], + "speckled calcifications in the end part of the 3rd toe bone": [ + "HP:0100064" + ], + "triangular epiphysis of the 3rd toe": [ + "HP:0100065" + ], + "triangular epiphyses of the 3rd toe": [ + "HP:0100065" + ], + "triangular end part of the 3rd toe bone": [ + "HP:0100065" + ], + "absent epiphysis of the 4th toe": [ + "HP:0100066" + ], + "absent epiphyses of the 4th toe": [ + "HP:0100066" + ], + "absent end part of the 4th toe bone": [ + "HP:0100066" + ], + "bracket epiphysis of the 4th toe": [ + "HP:0100067" + ], + "bracket epiphyses of the 4th toe": [ + "HP:0100067" + ], + "bracket shape end part of 4th toe bone": [ + "HP:0100067" + ], + "bracket shaped end part of 4th toe bone": [ + "HP:0100067" + ], + "cone - shaped epiphysis of the 4th toe": [ + "HP:0100068" + ], + "cone - shaped epiphyses of the 4th toe": [ + "HP:0100068" + ], + "cone - shaped end part of the 4th toe bone": [ + "HP:0100068" + ], + "enlarged epiphysis of the 4th toe": [ + "HP:0100069" + ], + "enlarged epiphyses of the 4th toe": [ + "HP:0100069" + ], + "enlarged end part of the 4th toe bone": [ + "HP:0100069" + ], + "fragmentation of the epiphysis of the 4th toe": [ + "HP:0100070" + ], + "fragmentation of the epiphyses of the 4th toe": [ + "HP:0100070" + ], + "fragmentation of the end part of the 4th toe bone": [ + "HP:0100070" + ], + "irregular epiphysis of the 4th toe": [ + "HP:0100071" + ], + "irregular epiphyses of the 4th toe": [ + "HP:0100071" + ], + "irregular end part of the 4th toe bone": [ + "HP:0100071" + ], + "ivory epiphysis of the 4th toe": [ + "HP:0100072" + ], + "ivory epiphyses of the 4th toe": [ + "HP:0100072" + ], + "increase bone density of end part of the 4th toe bone": [ + "HP:0100072" + ], + "increased bone density of end part of the 4th toe bone": [ + "HP:0100072" + ], + "pseudoepiphyses of the 4th toe": [ + "HP:0100073" + ], + "small epiphysis of the 4th toe": [ + "HP:0100074" + ], + "small epiphyses of the 4th toe": [ + "HP:0100074" + ], + "small end part of the 4th toe bone": [ + "HP:0100074" + ], + "stippling of the epiphysis of the 4th toe": [ + "HP:0100075" + ], + "stippling of the epiphyses of the 4th toe": [ + "HP:0100075" + ], + "speckled calcification in the end part of the 4th toe bone": [ + "HP:0100075" + ], + "speckled calcifications in the end part of the 4th toe bone": [ + "HP:0100075" + ], + "triangular epiphysis of the 4th toe": [ + "HP:0100076" + ], + "triangular epiphyses of the 4th toe": [ + "HP:0100076" + ], + "triangular end part of the 4th toe bone": [ + "HP:0100076" + ], + "absent epiphysis of the 5th toe": [ + "HP:0100077" + ], + "absent epiphyses of the 5th toe": [ + "HP:0100077" + ], + "absent end part of the little toe bone": [ + "HP:0100077" + ], + "absent end part of the pinkie toe bone": [ + "HP:0100077" + ], + "absent end part of the pinky toe bone": [ + "HP:0100077" + ], + "bracket epiphysis of the 5th toe": [ + "HP:0100078" + ], + "bracket epiphyses of the 5th toe": [ + "HP:0100078" + ], + "bracket shape end part of little toe bone": [ + "HP:0100078" + ], + "bracket shaped end part of little toe bone": [ + "HP:0100078" + ], + "bracket shape end part of pinkie toe bone": [ + "HP:0100078" + ], + "bracket shaped end part of pinkie toe bone": [ + "HP:0100078" + ], + "bracket shape end part of pinky toe bone": [ + "HP:0100078" + ], + "bracket shaped end part of pinky toe bone": [ + "HP:0100078" + ], + "cone - shaped epiphysis of the 5th toe": [ + "HP:0100079" + ], + "cone - shaped epiphyses of the 5th toe": [ + "HP:0100079" + ], + "cone - shaped end part of the little toe bone": [ + "HP:0100079" + ], + "cone - shaped end part of the pinkie toe bone": [ + "HP:0100079" + ], + "cone - shaped end part of the pinky toe bone": [ + "HP:0100079" + ], + "enlarged epiphysis of the 5th toe": [ + "HP:0100080" + ], + "enlarged epiphyses of the 5th toe": [ + "HP:0100080" + ], + "enlarged end part of the little toe bone": [ + "HP:0100080" + ], + "enlarged end part of the pinkie toe bone": [ + "HP:0100080" + ], + "enlarged end part of the pinky toe bone": [ + "HP:0100080" + ], + "fragmentation of the epiphysis of the 5th toe": [ + "HP:0100081" + ], + "fragmentation of the epiphyses of the 5th toe": [ + "HP:0100081" + ], + "fragmentation of the end part of the little toe bone": [ + "HP:0100081" + ], + "fragmentation of the end part of the pinkie toe bone": [ + "HP:0100081" + ], + "fragmentation of the end part of the pinky toe bone": [ + "HP:0100081" + ], + "irregular epiphysis of the 5th toe": [ + "HP:0100082" + ], + "irregular epiphyses of the 5th toe": [ + "HP:0100082" + ], + "irregular end part of the little toe bone": [ + "HP:0100082" + ], + "irregular end part of the pinkie toe bone": [ + "HP:0100082" + ], + "irregular end part of the pinky toe bone": [ + "HP:0100082" + ], + "ivory epiphysis of the 5th toe": [ + "HP:0100083" + ], + "ivory epiphyses of the 5th toe": [ + "HP:0100083" + ], + "increase bone density of end part of the little toe bone": [ + "HP:0100083" + ], + "increased bone density of end part of the little toe bone": [ + "HP:0100083" + ], + "increase bone density of end part of the pinkie toe bone": [ + "HP:0100083" + ], + "increased bone density of end part of the pinkie toe bone": [ + "HP:0100083" + ], + "increase bone density of end part of the pinky toe bone": [ + "HP:0100083" + ], + "increased bone density of end part of the pinky toe bone": [ + "HP:0100083" + ], + "pseudoepiphyses of the 5th toe": [ + "HP:0100084" + ], + "small epiphysis of the 5th toe": [ + "HP:0100085" + ], + "small epiphyses of the 5th toe": [ + "HP:0100085" + ], + "small end part of the little toe bone": [ + "HP:0100085" + ], + "small end part of the pinkie toe bone": [ + "HP:0100085" + ], + "small end part of the pinky toe bone": [ + "HP:0100085" + ], + "stippling of the epiphysis of the 5th toe": [ + "HP:0100086" + ], + "stippling of the epiphyses of the 5th toe": [ + "HP:0100086" + ], + "speckled calcification in the end part of the little toe bone": [ + "HP:0100086" + ], + "speckled calcifications in the end part of the little toe bone": [ + "HP:0100086" + ], + "speckled calcification in the end part of the pinkie toe bone": [ + "HP:0100086" + ], + "speckled calcifications in the end part of the pinkie toe bone": [ + "HP:0100086" + ], + "speckled calcification in the end part of the pinky toe bone": [ + "HP:0100086" + ], + "speckled calcifications in the end part of the pinky toe bone": [ + "HP:0100086" + ], + "triangular epiphysis of the 5th toe": [ + "HP:0100087" + ], + "triangular epiphyses of the 5th toe": [ + "HP:0100087" + ], + "triangular end part of the little toe bone": [ + "HP:0100087" + ], + "triangular end part of the pinkie toe bone": [ + "HP:0100087" + ], + "triangular end part of the pinky toe bone": [ + "HP:0100087" + ], + "abnormality of the epiphysis of the distal phalanx of the 2nd toe": [ + "HP:0100088" + ], + "abnormality of the end part of the outermost bone of the 2nd toe": [ + "HP:0100088" + ], + "abnormality of the epiphysis of the middle phalanx of the 2nd toe": [ + "HP:0100089" + ], + "abnormality of the end part of the middle bone of the 2nd toe": [ + "HP:0100089" + ], + "abnormality of the epiphysis of the proximal phalanx of the 2nd toe": [ + "HP:0100090" + ], + "abnormality of the end part of the innermost bone of the 2nd toe": [ + "HP:0100090" + ], + "abnormality of the epiphysis of the distal phalanx of the 3rd toe": [ + "HP:0100091" + ], + "abnormality of the end part of the outermost bone of the 3rd toe": [ + "HP:0100091" + ], + "abnormality of the epiphysis of the middle phalanx of the 3rd toe": [ + "HP:0100092" + ], + "abnormality of the end part of the middle bone of the 3rd toe": [ + "HP:0100092" + ], + "abnormality of the epiphysis of the proximal phalanx of the 3rd toe": [ + "HP:0100093" + ], + "abnormality of the end part of the innermost bone of the 3rd toe": [ + "HP:0100093" + ], + "abnormality of the epiphysis of the distal phalanx of the 4th toe": [ + "HP:0100094" + ], + "abnormality of the end part of the outermost bone of the 4th toe": [ + "HP:0100094" + ], + "abnormality of the epiphysis of the middle phalanx of the 4th toe": [ + "HP:0100095" + ], + "abnormality of the end part of the middle bone of the 4th toe": [ + "HP:0100095" + ], + "abnormality of the epiphysis of the proximal phalanx of the 4th toe": [ + "HP:0100096" + ], + "abnormality of the end part of the innermost bone of the 4th toe": [ + "HP:0100096" + ], + "abnormality of the epiphysis of the distal phalanx of the 5th toe": [ + "HP:0100097" + ], + "abnormality of the end part of the outermost bone of the little toe": [ + "HP:0100097" + ], + "abnormality of the end part of the outermost bone of the pinkie toe": [ + "HP:0100097" + ], + "abnormality of the end part of the outermost bone of the pinky toe": [ + "HP:0100097" + ], + "abnormality of the epiphysis of the middle phalanx of the 5th toe": [ + "HP:0100098" + ], + "abnormality of the end part of the middle bone of the little toe": [ + "HP:0100098" + ], + "abnormality of the end part of the middle bone of the pinkie toe": [ + "HP:0100098" + ], + "abnormality of the end part of the middle bone of the pinky toe": [ + "HP:0100098" + ], + "abnormality of the epiphysis of the proximal phalanx of the 5th toe": [ + "HP:0100099" + ], + "abnormality of the end part of the innermost bone of the little toe": [ + "HP:0100099" + ], + "abnormality of the end part of the innermost bone of the pinkie toe": [ + "HP:0100099" + ], + "abnormality of the end part of the innermost bone of the pinky toe": [ + "HP:0100099" + ], + "absent epiphysis of the distal phalanx of the 2nd toe": [ + "HP:0100100" + ], + "absent end part of the outermost bone of the 2nd toe": [ + "HP:0100100" + ], + "bracket epiphysis of the distal phalanx of the 2nd toe": [ + "HP:0100101" + ], + "bracket shape end part of the outermost bone of the 2nd toe": [ + "HP:0100101" + ], + "bracket shaped end part of the outermost bone of the 2nd toe": [ + "HP:0100101" + ], + "cone - shaped epiphysis of the distal phalanx of the 2nd toe": [ + "HP:0100102" + ], + "cone - shaped end part of the outermost bone of the 2nd toe": [ + "HP:0100102" + ], + "enlarged epiphysis of the distal phalanx of the 2nd toe": [ + 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epiphysis of the distal phalanx of the 2nd toe": [ + "HP:0100109" + ], + "speckled calcification in the end part of the outermost bone of the 2nd toe": [ + "HP:0100109" + ], + "speckled calcifications in the end part of the outermost bone of the 2nd toe": [ + "HP:0100109" + ], + "triangular epiphysis of the distal phalanx of the 2nd toe": [ + "HP:0100110" + ], + "triangular end part of the outermost bone of the 2nd toe": [ + "HP:0100110" + ], + "absent epiphysis of the middle phalanx of the 2nd toe": [ + "HP:0100111" + ], + "absent end part of the middle bone of the 2nd toe": [ + "HP:0100111" + ], + "bracket epiphysis of the middle phalanx of the 2nd toe": [ + "HP:0100112" + ], + "bracket shape end part of the middle bone of the 2nd toe": [ + "HP:0100112" + ], + "bracket shaped end part of the middle bone of the 2nd toe": [ + "HP:0100112" + ], + "cone - shaped epiphysis of the middle phalanx of the 2nd toe": [ + "HP:0100113" + ], + "cone - shaped end part of the middle bone of the 2nd 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middle bone of the 2nd toe": [ + "HP:0100119" + ], + "stippling of the epiphysis of the middle phalanx of the 2nd toe": [ + "HP:0100120" + ], + "speckled calcification in of the end part of the middle bone of the 2nd toe": [ + "HP:0100120" + ], + "speckled calcifications in of the end part of the middle bone of the 2nd toe": [ + "HP:0100120" + ], + "triangular epiphysis of the middle phalanx of the 2nd toe": [ + "HP:0100121" + ], + "triangular end part of the middle bone of the 2nd toe": [ + "HP:0100121" + ], + "absent epiphysis of the proximal phalanx of the 2nd toe": [ + "HP:0100122" + ], + "absent end part of the innermost bone of the 2nd toe": [ + "HP:0100122" + ], + "bracket epiphysis of the proximal phalanx of the 2nd toe": [ + "HP:0100123" + ], + "bracket shape end part of the innermost bone of the 2nd toe": [ + "HP:0100123" + ], + "bracket shaped end part of the innermost bone of the 2nd toe": [ + "HP:0100123" + ], + "cone - shaped epiphysis of the proximal phalanx of the 2nd toe": [ + "HP:0100124" + ], + "cone - shaped end part of the innermost bone of the 2nd toe": [ + "HP:0100124" + ], + "enlarged epiphysis of the proximal phalanx of the 2nd toe": [ + "HP:0100125" + ], + "enlarged end part of the innermost bone of the 2nd toe": [ + "HP:0100125" + ], + "fragmentation of the epiphysis of the proximal phalanx of the 2nd toe": [ + "HP:0100126" + ], + "fragmentation of the end part of the innermost bone of the 2nd toe": [ + "HP:0100126" + ], + "irregular epiphysis of the proximal phalanx of the 2nd toe": [ + "HP:0100127" + ], + "irregular end part of the innermost bone of the 2nd toe": [ + "HP:0100127" + ], + "ivory epiphysis of the proximal phalanx of the 2nd toe": [ + "HP:0100128" + ], + "increase bone density of end part of the innermost bone of the 2nd toe": [ + "HP:0100128" + ], + "increased bone density of end part of the innermost bone of the 2nd toe": [ + "HP:0100128" + ], + "pseudoepiphysis of the proximal phalanx of the 2nd toe": [ + "HP:0100129" + 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outermost bone of the 3rd toe": [ + "HP:0100141" + ], + "increased bone density of end part of the outermost bone of the 3rd toe": [ + "HP:0100141" + ], + "pseudoepiphysis of the distal phalanx of the 3rd toe": [ + "HP:0100142" + ], + "small epiphysis of the distal phalanx of the 3rd toe": [ + "HP:0100143" + ], + "small end part of the outermost bone of the 3rd toe": [ + "HP:0100143" + ], + "stippling of the epiphysis of the distal phalanx of the 3rd toe": [ + "HP:0100144" + ], + "speckled calcification in the end part of the outermost bone of the 3rd toe": [ + "HP:0100144" + ], + "speckled calcifications in the end part of the outermost bone of the 3rd toe": [ + "HP:0100144" + ], + "triangular epiphysis of the distal phalanx of the 3rd toe": [ + "HP:0100145" + ], + "triangular end part of the outermost bone of the 3rd toe": [ + "HP:0100145" + ], + "absent epiphysis of the middle phalanx of the 3rd toe": [ + "HP:0100146" + ], + "absent end part of the middle bone of the 3rd toe": [ + 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toe": [ + "HP:0100152" + ], + "increase bone density of end part of the middle bone of the 3rd toe": [ + "HP:0100152" + ], + "increased bone density of end part of the middle bone of the 3rd toe": [ + "HP:0100152" + ], + "pseudoepiphysis of the middle phalanx of the 3rd toe": [ + "HP:0100153" + ], + "small epiphysis of the middle phalanx of the 3rd toe": [ + "HP:0100154" + ], + "small end part of the middle bone of the 3rd toe": [ + "HP:0100154" + ], + "stippling of the epiphysis of the middle phalanx of the 3rd toe": [ + "HP:0100155" + ], + "speckled calcification in the end part of the middle bone of the 3rd toe": [ + "HP:0100155" + ], + "speckled calcifications in the end part of the middle bone of the 3rd toe": [ + "HP:0100155" + ], + "triangular epiphysis of the middle phalanx of the 3rd toe": [ + "HP:0100156" + ], + "triangular end part of the middle bone of the 3rd toe": [ + "HP:0100156" + ], + "absent epiphysis of the proximal phalanx of the 3rd toe": [ + "HP:0100157" + ], + 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3rd toe": [ + "HP:0100162" + ], + "ivory epiphysis of the proximal phalanx of the 3rd toe": [ + "HP:0100163" + ], + "increase bone density of end part of the innermost bone of the 3rd toe": [ + "HP:0100163" + ], + "increased bone density of end part of the innermost bone of the 3rd toe": [ + "HP:0100163" + ], + "pseudoepiphysis of the proximal phalanx of the 3rd toe": [ + "HP:0100164" + ], + "small epiphysis of the proximal phalanx of the 3rd toe": [ + "HP:0100165" + ], + "small end part of the innermost bone of the 3rd toe": [ + "HP:0100165" + ], + "stippling of the epiphysis of the proximal phalanx of the 3rd toe": [ + "HP:0100166" + ], + "speckled calcification in of the end part of the innermost bone of the 3rd toe": [ + "HP:0100166" + ], + "speckled calcifications in of the end part of the innermost bone of the 3rd toe": [ + "HP:0100166" + ], + "triangular epiphysis of the proximal phalanx of the 3rd toe": [ + "HP:0100167" + ], + "triangular end part of the innermost bone of the 3rd toe": [ + "HP:0100167" + ], + "fragment epiphysis": [ + "HP:0100168" + ], + "fragmented epiphyses": [ + "HP:0100168" + ], + "fragmented end part of bone": [ + "HP:0100168" + ], + "absent epiphysis of the distal phalanx of the 4th toe": [ + "HP:0100169" + ], + "absent end part of the outermost bone of the 4th toe": [ + "HP:0100169" + ], + "bracket epiphysis of the distal phalanx of the 4th toe": [ + "HP:0100170" + ], + "bracket shape end part of the outermost bone of the 4th toe": [ + "HP:0100170" + ], + "bracket shaped end part of the outermost bone of the 4th toe": [ + "HP:0100170" + ], + "cone - shaped epiphysis of the distal phalanx of the 4th toe": [ + "HP:0100171" + ], + "cone - shaped end part of the outermost bone of the 4th toe": [ + "HP:0100171" + ], + "enlarged epiphysis of the distal phalanx of the 4th toe": [ + "HP:0100172" + ], + "enlarged end part of the outermost bone of the 4th toe": [ + "HP:0100172" + ], + "fragmentation of the epiphysis of the distal phalanx of the 4th toe": [ + "HP:0100173" + ], + "fragmentation of the end part of the outermost bone of the 4th toe": [ + "HP:0100173" + ], + "irregular epiphysis of the distal phalanx of the 4th toe": [ + "HP:0100174" + ], + "irregular end part of the outermost bone of the 4th toe": [ + "HP:0100174" + ], + "ivory epiphysis of the distal phalanx of the 4th toe": [ + "HP:0100175" + ], + "increase bone density of end part of the outermost bone of the 4th toe": [ + "HP:0100175" + ], + "increased bone density of end part of the outermost bone of the 4th toe": [ + "HP:0100175" + ], + "pseudoepiphysis of the distal phalanx of the 4th toe": [ + "HP:0100176" + ], + "small epiphysis of the distal phalanx of the 4th toe": [ + "HP:0100177" + ], + "small end part of the outermost bone of the 4th toe": [ + "HP:0100177" + ], + "stippling of the epiphysis of the distal phalanx of the 4th toe": [ + "HP:0100178" + ], + "speckled calcification in the end part of the outermost bone of the 4th toe": [ + 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calcification in the end part of the middle bone of the 4th toe": [ + "HP:0100189" + ], + "speckled calcifications in the end part of the middle bone of the 4th toe": [ + "HP:0100189" + ], + "triangular epiphysis of the middle phalanx of the 4th toe": [ + "HP:0100190" + ], + "triangular end part of the middle bone of the 4th toe": [ + "HP:0100190" + ], + "absent epiphysis of the proximal phalanx of the 4th toe": [ + "HP:0100191" + ], + "absent end part of the innermost bone of the 4th toe": [ + "HP:0100191" + ], + "bracket epiphysis of the proximal phalanx of the 4th toe": [ + "HP:0100192" + ], + "bracket shape end part of the innermost bone of 4th toe": [ + "HP:0100192" + ], + "bracket shaped end part of the innermost bone of 4th toe": [ + "HP:0100192" + ], + "cone - shaped epiphysis of the proximal phalanx of the 4th toe": [ + "HP:0100193" + ], + "cone - shaped end part of the innermost bone of the 4th toe": [ + "HP:0100193" + ], + "enlarged epiphysis of the proximal phalanx of the 4th toe": [ + "HP:0100194" + ], + "enlarged end part of the innermost bone of the 4th toe": [ + "HP:0100194" + ], + "fragmentation of the epiphysis of the proximal phalanx of the 4th toe": [ + "HP:0100195" + ], + "fragmentation of the end part of the innermost bone of the 4th toe": [ + "HP:0100195" + ], + "irregular epiphysis of the proximal phalanx of the 4th toe": [ + "HP:0100196" + ], + "irregular end part of the innermost bone of the 4th toe": [ + "HP:0100196" + ], + "ivory epiphysis of the proximal phalanx of the 4th toe": [ + "HP:0100197" + ], + "increase bone density of end part of the innermost bone of the 4th toe": [ + "HP:0100197" + ], + "increased bone density of end part of the innermost bone of the 4th toe": [ + "HP:0100197" + ], + "pseudoepiphysis of the proximal phalanx of the 4th toe": [ + "HP:0100198" + ], + "small epiphysis of the proximal phalanx of the 4th toe": [ + "HP:0100199" + ], + "small end part of the innermost bone of the 4th toe": [ + "HP:0100199" + ], + 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pinkie toe": [ + "HP:0100205" + ], + "enlarged end part of the outermost bone of the pinky toe": [ + "HP:0100205" + ], + "fragmentation of the epiphysis of the distal phalanx of the 5th toe": [ + "HP:0100206" + ], + "fragmentation of the end part of the outermost bone of the little toe": [ + "HP:0100206" + ], + "fragmentation of the end part of the outermost bone of the pinkie toe": [ + "HP:0100206" + ], + "fragmentation of the end part of the outermost bone of the pinky toe": [ + "HP:0100206" + ], + "irregular epiphysis of the distal phalanx of the 5th toe": [ + "HP:0100207" + ], + "irregular end part of the outermost bone of the little toe": [ + "HP:0100207" + ], + "irregular end part of the outermost bone of the pinkie toe": [ + "HP:0100207" + ], + "irregular end part of the outermost bone of the pinky toe": [ + "HP:0100207" + ], + "ivory epiphysis of the distal phalanx of the 5th toe": [ + "HP:0100208" + ], + "increase bone density of end part of the outermost bone of the little toe": [ + "HP:0100208" + ], + "increased bone density of end part of the outermost bone of the little toe": [ + "HP:0100208" + ], + "increase bone density of end part of the outermost bone of the pinkie toe": [ + "HP:0100208" + ], + "increased bone density of end part of the outermost bone of the pinkie toe": [ + "HP:0100208" + ], + "increase bone density of end part of the outermost bone of the pinky toe": [ + "HP:0100208" + ], + "increased bone density of end part of the outermost bone of the pinky toe": [ + "HP:0100208" + ], + "pseudoepiphysis of the distal phalanx of the 5th toe": [ + "HP:0100209" + ], + "small epiphysis of the distal phalanx of the 5th toe": [ + "HP:0100210" + ], + "small end part of the outermost bone of the little toe": [ + "HP:0100210" + ], + "small end part of the outermost bone of the pinkie toe": [ + "HP:0100210" + ], + "small end part of the outermost bone of the pinky toe": [ + "HP:0100210" + ], + "stippling of the epiphysis of the distal phalanx of the 5th toe": [ + "HP:0100211" + ], + "speckled calcification in the end part of the outermost bone of the little toe": [ + "HP:0100211" + ], + "speckled calcifications in the end part of the outermost bone of the little toe": [ + "HP:0100211" + ], + "speckled calcification in the end part of the outermost bone of the pinkie toe": [ + "HP:0100211" + ], + "speckled calcifications in the end part of the outermost bone of the pinkie toe": [ + "HP:0100211" + ], + "speckled calcification in the end part of the outermost bone of the pinky toe": [ + "HP:0100211" + ], + "speckled calcifications in the end part of the outermost bone of the pinky toe": [ + "HP:0100211" + ], + "triangular epiphysis of the distal phalanx of the 5th toe": [ + "HP:0100212" + ], + "triangular end part of the outermost bone of the little toe": [ + "HP:0100212" + ], + "triangular end part of the outermost bone of the pinkie toe": [ + "HP:0100212" + ], + "triangular end part of the outermost bone of the pinky toe": [ + "HP:0100212" + ], + "absent epiphysis of the middle phalanx of the 5th toe": [ + "HP:0100213" + ], + "absent end part of the middle bone of the little toe": [ + "HP:0100213" + ], + "absent end part of the middle bone of the pinkie toe": [ + "HP:0100213" + ], + "absent end part of the middle bone of the pinky toe": [ + "HP:0100213" + ], + "bracket epiphysis of the middle phalanx of the 5th toe": [ + "HP:0100214" + ], + "bracket shape end part of the middle bone of the little toe": [ + "HP:0100214" + ], + "bracket shaped end part of the middle bone of the little toe": [ + "HP:0100214" + ], + "bracket shape end part of the middle bone of the pinkie toe": [ + "HP:0100214" + ], + "bracket shaped end part of the middle bone of the pinkie toe": [ + "HP:0100214" + ], + "bracket shape end part of the middle bone of the pinky toe": [ + "HP:0100214" + ], + "bracket shaped end part of the middle bone of the pinky toe": [ + "HP:0100214" + ], + "cone - shaped epiphysis of the middle phalanx of the 5th toe": [ + "HP:0100215" + ], + "cone - shaped end part of the middle bone of the little toe": [ + "HP:0100215" + ], + "cone - shaped end part of the middle bone of the pinkie toe": [ + "HP:0100215" + ], + "cone - shaped end part of the middle bone of the pinky toe": [ + "HP:0100215" + ], + "enlarged epiphysis of the middle phalanx of the 5th toe": [ + "HP:0100216" + ], + "enlarged end part of the middle bone of the little toe": [ + "HP:0100216" + ], + "enlarged end part of the middle bone of the pinkie toe": [ + "HP:0100216" + ], + "enlarged end part of the middle bone of the pinky toe": [ + "HP:0100216" + ], + "fragmentation of the epiphysis of the middle phalanx of the 5th toe": [ + "HP:0100217" + ], + "fragmentation of the end part of the middle bone of the little toe": [ + "HP:0100217" + ], + "fragmentation of the end part of the middle bone of the pinkie toe": [ + "HP:0100217" + ], + "fragmentation of the end part of the middle bone of the pinky toe": [ + "HP:0100217" + ], + "irregular epiphysis of the middle phalanx of the 5th toe": [ + "HP:0100218" + ], + "irregular end part of the middle bone of the little toe": [ + "HP:0100218" + ], + "irregular end part of the middle bone of the pinkie toe": [ + "HP:0100218" + ], + "irregular end part of the middle bone of the pinky toe": [ + "HP:0100218" + ], + "ivory epiphysis of the middle phalanx of the 5th toe": [ + "HP:0100219" + ], + "increase bone density of end part of the middle bone of the little toe": [ + "HP:0100219" + ], + "increased bone density of end part of the middle bone of the little toe": [ + "HP:0100219" + ], + "increase bone density of end part of the middle bone of the pinkie toe": [ + "HP:0100219" + ], + "increased bone density of end part of the middle bone of the pinkie toe": [ + "HP:0100219" + ], + "increase bone density of end part of the middle bone of the pinky toe": [ + "HP:0100219" + ], + "increased bone density of end part of the middle bone of the pinky toe": [ + "HP:0100219" + ], + "pseudoepiphysis of the middle phalanx of the 5th toe": [ + "HP:0100220" + ], + "small epiphysis of the middle phalanx of the 5th toe": [ + "HP:0100221" + ], + "small end part of the middle bone of the little toe": [ + "HP:0100221" + ], + "small end part of the middle bone of the pinkie toe": [ + "HP:0100221" + ], + "small end part of the middle bone of the pinky toe": [ + "HP:0100221" + ], + "stippling of the epiphysis of the middle phalanx of the 5th toe": [ + "HP:0100222" + ], + "speckled calcification in end part of the innermost bone of the pinkie toe": [ + "HP:0100222" + ], + "speckled calcifications in end part of the innermost bone of the pinkie toe": [ + "HP:0100222" + ], + "speckled calcification in middle part of the innermost bone of the little toe": [ + "HP:0100222" + ], + "speckled calcifications in middle part of the innermost bone of the little toe": [ + "HP:0100222" + ], + "speckled calcification in middle part of the innermost bone of the pinky toe": [ + "HP:0100222" + ], + "speckled calcifications in middle part of the innermost bone of the pinky toe": [ + "HP:0100222" + ], + "triangular epiphysis of the middle phalanx of the 5th toe": [ + "HP:0100223" + ], + "triangular end part of the middle bone of the little toe": [ + "HP:0100223" + ], + "triangular end part of the middle bone of the pinkie toe": [ + "HP:0100223" + ], + "triangular end part of the middle bone of the pinky toe": [ + "HP:0100223" + ], + "absent epiphysis of the proximal phalanx of the 5th toe": [ + "HP:0100224" + ], + "absent end part of the innermost bone of the little toe": [ + "HP:0100224" + ], + "absent end part of the innermost bone of the pinkie toe": [ + "HP:0100224" + ], + "absent end part of the innermost bone of the pinky toe": [ + "HP:0100224" + ], + "bracket epiphysis of the proximal phalanx of the 5th toe": [ + "HP:0100225" + ], + "bracket shape end part of the innermost bone of the little toe": [ + "HP:0100225" + ], + "bracket shaped end part of the innermost bone of the little toe": [ + "HP:0100225" + ], + "bracket shape end part of the innermost bone of the pinkie toe": [ + "HP:0100225" + ], + "bracket shaped end part of the innermost bone of the pinkie toe": [ + "HP:0100225" + ], + "bracket shape end part of the innermost bone of the pinky toe": [ + "HP:0100225" + ], + "bracket shaped end part of the innermost bone of the pinky toe": [ + "HP:0100225" + ], + "cone - shaped epiphysis of the proximal phalanx of the 5th toe": [ + "HP:0100226" + ], + "cone - shaped end part of the innermost bone of the little toe": [ + "HP:0100226" + ], + "cone - shaped end part of the innermost bone of the pinkie toe": [ + "HP:0100226" + ], + "cone - shaped end part of the innermost bone of the pinky toe": [ + "HP:0100226" + ], + "enlarged epiphysis of the proximal phalanx of the 5th toe": [ + "HP:0100227" + ], + "enlarged end part of the innermost bone of the little toe": [ + "HP:0100227" + ], + "enlarged end part of the innermost bone of the pinkie toe": [ + "HP:0100227" + ], + "enlarged end part of the innermost bone of the pinky toe": [ + "HP:0100227" + ], + "fragmentation of the epiphysis of the proximal phalanx of the 5th toe": [ + "HP:0100228" + ], + "fragmentation of the end part of the innermost bone of the little toe": [ + "HP:0100228" + ], + "fragmentation of the end part of the innermost bone of the pinkie toe": [ + "HP:0100228" + ], + "fragmentation of the end part of the innermost bone of the pinky toe": [ + "HP:0100228" + ], + "irregular epiphysis of the proximal phalanx of the 5th toe": [ + "HP:0100229" + ], + "irregular end part of the innermost bone of the little toe": [ + "HP:0100229" + ], + "irregular end part of the innermost bone of the pinkie toe": [ + "HP:0100229" + ], + "irregular end part of the innermost bone of the pinky toe": [ + "HP:0100229" + ], + "ivory epiphysis of the proximal phalanx of the 5th toe": [ + "HP:0100230" + ], + "increase bone density of end part of the innermost bone of the little toe": [ + "HP:0100230" + ], + "increased bone density of end part of the innermost bone of the little toe": [ + "HP:0100230" + ], + "increase bone density of end part of the innermost bone of the pinkie toe": [ + "HP:0100230" + ], + "increased bone density of end part of the innermost bone of the pinkie toe": [ + "HP:0100230" + ], + "increase bone density of end part of the innermost bone of the pinky toe": [ + "HP:0100230" + ], + "increased bone density of end part of the innermost bone of the pinky toe": [ + "HP:0100230" + ], + "pseudoepiphysis of the proximal phalanx of the 5th toe": [ + "HP:0100231" + ], + "small epiphysis of the proximal phalanx of the 5th toe": [ + "HP:0100232" + ], + "small end part of the innermost bone of the little toe": [ + "HP:0100232" + ], + "small end part of the innermost bone of the pinkie toe": [ + "HP:0100232" + ], + "small end part of the innermost bone of the pinky toe": [ + "HP:0100232" + ], + "stippling of the epiphysis of the proximal phalanx of the 5th toe": [ + "HP:0100233" + ], + "speckled calcification in the end part of the innermost bone of the little toe": [ + "HP:0100233" + ], + "speckled calcifications in the end part of the innermost bone of the little toe": [ + "HP:0100233" + ], + "speckled calcification in the end part of the innermost bone of the pinkie toe": [ + "HP:0100233" + ], + "speckled calcifications in the end part of the innermost bone of the pinkie toe": [ + "HP:0100233" + ], + "speckled calcification in the end part of the innermost bone of the pinky toe": [ + "HP:0100233" + ], + "speckled calcifications in the end part of the innermost bone of the pinky toe": [ + "HP:0100233" + ], + "triangular epiphysis of the proximal phalanx of the 5th toe": [ + "HP:0100234" + ], + "triangular end part of the innermost bone of the little toe": [ + "HP:0100234" + ], + "triangular end part of the innermost bone of the pinkie toe": [ + "HP:0100234" + ], + "triangular end part of the innermost bone of the pinky toe": [ + "HP:0100234" + ], + "synostosis involve bone of the toe": [ + "HP:0100235" + ], + "synostosis involving bones of the toes": [ + "HP:0100235" + ], + "fusion involve bone of the toe": [ + "HP:0100235" + ], + "fusion involving bones of the toes": [ + "HP:0100235" + ], + "proximal foot symphalangism": [ + "HP:0100237" + ], + "synostosis involve bone of the upper limb": [ + "HP:0100238" + ], + "synostosis involving bones of the upper limbs": [ + "HP:0100238" + ], + "fusion involve bone of the upper limb": [ + "HP:0100238" + ], + "fusion involving bones of the upper limbs": [ + "HP:0100238" + ], + "synostosis of joint": [ + "HP:0100240" + ], + "synostosis of joints": [ + "HP:0100240" + ], + "bony ankylosis": [ + "HP:0100240" + ], + "fusion of joint": [ + "HP:0100240" + ], + "fusion of joints": [ + "HP:0100240" + ], + "ectopic respiratory mucosa": [ + "HP:0100241" + ], + "sarcoma": [ + "HP:0100242" + ], + "cancer of connective tissue": [ + "HP:0100242" + ], + "malignant connective tissue tumor": [ + "HP:0100242" + ], + "malignant connective tissue tumour": [ + "HP:0100242" + ], + "leiomyosarcoma": [ + "HP:0100243" + ], + "fibrosarcoma": [ + "HP:0100244" + ], + "desmoid tumor": [ + "HP:0100245" + ], + "desmoid tumors": [ + "HP:0100245" + ], + "desmoid tumour": [ + "HP:0100245" + ], + "desmoid tumours": [ + "HP:0100245" + ], + "osteoma": [ + "HP:0100246" + ], + "recurrent singultus": [ + "HP:0100247" + ], + "hiccup": [ + "HP:0100247" + ], + "hiccups": [ + "HP:0100247" + ], + "recurrent hiccough": [ + "HP:0100247" + ], + "recurrent hiccup": [ + "HP:0100247" + ], + "recurrent synchronous diaphragmatic flutter": [ + "HP:0100247" + ], + "hemiballismus": [ + "HP:0100248" + ], + "ballismus": [ + "HP:0100248" + ], + "calcification of muscle": [ + "HP:0100249" + ], + "calcification of muscles": [ + "HP:0100249" + ], + "skeletal muscle calcinosis": [ + "HP:0100249" + ], + "meningeal calcification": [ + "HP:0100250" + ], + "multiple central nervous system lipoma": [ + "HP:0100251" + ], + "multiple central nervous system lipomas": [ + "HP:0100251" + ], + "lipoma of the central nervous system": [ + "HP:0100251" + ], + "lipomas of the central nervous system": [ + "HP:0100251" + ], + "diaphyseal dysplasia": [ + "HP:0100252" + ], + "abnormality of the medullary cavity of the long bone": [ + "HP:0100253" + ], + "abnormality of the medullary cavity of the long bones": [ + "HP:0100253" + ], + "abnormality of the marrow cavity of the long bone": [ + "HP:0100253" + ], + "abnormality of the marrow cavity of the long bones": [ + "HP:0100253" + ], + "stenosis of the medullary cavity of the long bone": [ + "HP:0100254" + ], + "stenosis of the medullary cavity of the long bones": [ + "HP:0100254" + ], + "metaphyseal dysplasia": [ + "HP:0100255" + ], + "senile plaque": [ + "HP:0100256" + ], + "senile plaques": [ + "HP:0100256" + ], + "braindruse": [ + "HP:0100256" + ], + "neuritic plaque": [ + "HP:0100256" + ], + "neuritic plaques": [ + "HP:0100256" + ], + "senile druse": [ + "HP:0100256" + ], + "ectrodactyly": [ + "HP:0100257" + ], + "cleft hand": [ + "HP:0100257" + ], + "lobster claw hand": [ + "HP:0100257" + ], + "preaxial polydactyly": [ + "HP:0100258" + ], + "polydactyly , preaxial": [ + "HP:0100258" + ], + "postaxial polydactyly": [ + "HP:0100259" + ], + "polydactyly , postaxial": [ + "HP:0100259" + ], + "postaxial hexadactyly": [ + "HP:0100259" + ], + "mesoaxial polydactyly": [ + "HP:0100260" + ], + "central polydactyly": [ + "HP:0100260" + ], + "insertional polydactyly": [ + "HP:0100260" + ], + "intercalary polydactyly": [ + "HP:0100260" + ], + "abnormal tendon morphology": [ + "HP:0100261" + ], + "abnormal shape of tendon": [ + "HP:0100261" + ], + "abnormality of the sinew": [ + "HP:0100261" + ], + "synostosis involve digit": [ + "HP:0100262" + ], + "synostosis involving digits": [ + "HP:0100262" + ], + "fusion involve digit": [ + "HP:0100262" + ], + "fusion involving digits": [ + "HP:0100262" + ], + "distal symphalangism": [ + "HP:0100263" + ], + "symphalangism , distal": [ + "HP:0100263" + ], + "proximal symphalangism": [ + "HP:0100264" + ], + "cushing 's symphalangism": [ + "HP:0100264" + ], + "synostosis of metacarpal / metatarsal": [ + "HP:0100265" + ], + "synostosis of metacarpals / metatarsals": [ + "HP:0100265" + ], + "fusion of long bone of hand / long bone of foot": [ + "HP:0100265" + ], + "fusion of long bones of hand / long bones of foot": [ + "HP:0100265" + ], + "synostosis of carpal / tarsal": [ + "HP:0100266" + ], + "synostosis of carpals / tarsals": [ + "HP:0100266" + ], + "carpal and tarsal fusion": [ + "HP:0100266" + ], + "carpal and tarsal fusions": [ + "HP:0100266" + ], + "coalescence of carpal and tarsal bone": [ + "HP:0100266" + ], + "coalescence of carpal and tarsal bones": [ + "HP:0100266" + ], + "fusion of carpal and tarsal bone": [ + "HP:0100266" + ], + "fusion of carpal and tarsal bones": [ + "HP:0100266" + ], + "wrist bone / ankle bone fusion": [ + "HP:0100266" + ], + "wrist bone / ankle bone fusions": [ + "HP:0100266" + ], + "lip pit": [ + "HP:0100267" + ], + "upper lip pit": [ + "HP:0100268" + ], + "paramedian lip pit": [ + "HP:0100269" + ], + "paramedian labial pit": [ + "HP:0100269" + ], + "paramedian labial pits": [ + "HP:0100269" + ], + "abnormality of dorsoventral patterning of the limb": [ + "HP:0100270" + ], + "abnormality of dorsoventral patterning of the limbs": [ + "HP:0100270" + ], + "hyponasal speech": [ + "HP:0100271" + ], + "branchial sinus": [ + "HP:0100272" + ], + "branchial cleft sinus": [ + "HP:0100272" + ], + "neoplasm of the colon": [ + "HP:0100273" + ], + "colon tumor": [ + "HP:0100273" + ], + "colon tumour": [ + "HP:0100273" + ], + "gustatory lacrimation": [ + "HP:0100274" + ], + "diffuse cerebellar atrophy": [ + "HP:0100275" + ], + "skin pit": [ + "HP:0100276" + ], + "skin pits": [ + "HP:0100276" + ], + "periauricular skin pit": [ + "HP:0100277" + ], + "periauricular skin pits": [ + "HP:0100277" + ], + "periauricular earpits": [ + "HP:0100277" + ], + "periauricular fistula": [ + "HP:0100277" + ], + "periauricular fistulas": [ + "HP:0100277" + ], + "periauricular pit": [ + "HP:0100277" + ], + "periauricular pits": [ + "HP:0100277" + ], + "periauricular sinus": [ + "HP:0100277" + ], + "pit around the ear": [ + "HP:0100277" + ], + "pits around the ear": [ + "HP:0100277" + ], + "ulcerative colitis": [ + "HP:0100279" + ], + "colitis ulcerosa": [ + "HP:0100279" + ], + "crohn 's disease": [ + "HP:0100280" + ], + "granulomatous enteritis and colitis": [ + "HP:0100280" + ], + "morbus crohn": [ + "HP:0100280" + ], + "chronic colitis": [ + "HP:0100281" + ], + "acute colitis": [ + "HP:0100282" + ], + "emg : continuous motor unit activity at rest": [ + "HP:0100283" + ], + "emg : myotonic discharge": [ + "HP:0100284" + ], + "emg : myotonic discharges": [ + "HP:0100284" + ], + "emg : impaired neuromuscular transmission": [ + "HP:0100285" + ], + "emg : slow motor conduction": [ + "HP:0100287" + ], + "emg : myokymic discharge": [ + "HP:0100288" + ], + "emg : myokymic discharges": [ + "HP:0100288" + ], + "abnormality of pattern reversal visual evoke potential": [ + "HP:0100289" + ], + "abnormality of pattern reversal visual evoked potentials": [ + "HP:0100289" + ], + "abnormality of pattern reversal vep": [ + "HP:0100289" + ], + "abnormality of peripheral somatosensory evoke potential": [ + "HP:0100290" + ], + "abnormality of peripheral somatosensory evoked potentials": [ + "HP:0100290" + ], + "abnormality of central somatosensory evoke potential": [ + "HP:0100291" + ], + "abnormality of central somatosensory evoked potentials": [ + "HP:0100291" + ], + "amyloidosis of peripheral nerve": [ + "HP:0100292" + ], + "amyloidosis of peripheral nerves": [ + "HP:0100292" + ], + "muscle fiber hypertrophy": [ + "HP:0100293" + ], + "muscle fibre hypertrophy": [ + "HP:0100293" + ], + "muscle fiber atrophy": [ + "HP:0100295" + ], + "muscle fiber degeneration": [ + "HP:0100295" + ], + "muscle fibre atrophy": [ + "HP:0100295" + ], + "muscle fibre degeneration": [ + "HP:0100295" + ], + "perifascicular muscle fiber atrophy": [ + "HP:0100296" + ], + "perifascicular muscle fibre atrophy": [ + "HP:0100296" + ], + "increase endomysial connective tissue": [ + "HP:0100297" + ], + "increased endomysial connective tissue": [ + "HP:0100297" + ], + "motheaten muscle fiber": [ + "HP:0100298" + ], + "motheaten muscle fibers": [ + "HP:0100298" + ], + "motheaten muscle fibre": [ + "HP:0100298" + ], + "motheaten muscle fibres": [ + "HP:0100298" + ], + "muscle fiber inclusion body": [ + "HP:0100299" + ], + "muscle fiber inclusion bodies": [ + "HP:0100299" + ], + "muscle fibre inclusion body": [ + "HP:0100299" + ], + "muscle fibre inclusion bodies": [ + "HP:0100299" + ], + "desmin body": [ + "HP:0100300" + ], + "desmin bodies": [ + "HP:0100300" + ], + "muscle fiber tubular inclusion": [ + "HP:0100301" + ], + "muscle fiber tubular inclusions": [ + "HP:0100301" + ], + "muscle fiber tubular aggregate": [ + "HP:0100301" + ], + "muscle fiber tubular aggregates": [ + "HP:0100301" + ], + "muscle fibre tubular aggregate": [ + "HP:0100301" + ], + "muscle fibre tubular aggregates": [ + "HP:0100301" + ], + "muscle fibre tubular inclusion": [ + "HP:0100301" + ], + "muscle fibre tubular inclusions": [ + "HP:0100301" + ], + "muscle fiber tubuloreticular inclusion": [ + "HP:0100302" + ], + "muscle fiber tubuloreticular inclusions": [ + "HP:0100302" + ], + "muscle fiber tubuloreticular aggregate": [ + "HP:0100302" + ], + "muscle fiber tubuloreticular aggregates": [ + "HP:0100302" + ], + "muscle fibre tubuloreticular aggregate": [ + "HP:0100302" + ], + "muscle fibre tubuloreticular aggregates": [ + "HP:0100302" + ], + "muscle fibre tubuloreticular inclusion": [ + "HP:0100302" + ], + "muscle fibre tubuloreticular inclusions": [ + "HP:0100302" + ], + "muscle fiber cytoplasmatic inclusion body": [ + "HP:0100303" + ], + "muscle fiber cytoplasmatic inclusion bodies": [ + "HP:0100303" + ], + "muscle fiber cytoplasmic body": [ + "HP:0100303" + ], + "muscle fiber cytoplasmic bodies": [ + "HP:0100303" + ], + "muscle fibre cytoplasmatic inclusion body": [ + "HP:0100303" + ], + "muscle fibre cytoplasmatic inclusion bodies": [ + "HP:0100303" + ], + "muscle fibre cytoplasmic body": [ + "HP:0100303" + ], + "muscle fibre cytoplasmic bodies": [ + "HP:0100303" + ], + "muscle fiber intranuclear inclusion body": [ + "HP:0100304" + ], + "muscle fiber intranuclear inclusion bodies": [ + "HP:0100304" + ], + "muscle fibre intranuclear inclusion body": [ + "HP:0100304" + ], + "muscle fibre intranuclear inclusion bodies": [ + "HP:0100304" + ], + "ring fiber": [ + "HP:0100305" + ], + "ring fibers": [ + "HP:0100305" + ], + "ring fibre": [ + "HP:0100305" + ], + "ring fibres": [ + "HP:0100305" + ], + "muscle fiber hyaline body": [ + "HP:0100306" + ], + "muscle fiber hyaline bodies": [ + "HP:0100306" + ], + "muscle fibre hyaline body": [ + "HP:0100306" + ], + "muscle fibre hyaline bodies": [ + "HP:0100306" + ], + "cerebellar hemisphere hypoplasia": [ + "HP:0100307" + ], + "cerebral cortical hemiatrophy": [ + "HP:0100308" + ], + "subdural hemorrhage": [ + "HP:0100309" + ], + "subdural haematoma": [ + "HP:0100309" + ], + "subdural haemorrhage": [ + "HP:0100309" + ], + "subdural hematoma": [ + "HP:0100309" + ], + "epidural hemorrhage": [ + "HP:0100310" + ], + "epidural haematoma": [ + "HP:0100310" + ], + "epidural haemorrhage": [ + "HP:0100310" + ], + "epidural hematoma": [ + "HP:0100310" + ], + "extradural haematoma": [ + "HP:0100310" + ], + "extradural hematoma": [ + "HP:0100310" + ], + "cerebral ventricular adhesion": [ + "HP:0100311" + ], + "cerebral ventricular adhesions": [ + "HP:0100311" + ], + "cerebral germinoma": [ + "HP:0100312" + ], + "cerebral granulomatosis": [ + "HP:0100313" + ], + "cerebral inclusion body": [ + "HP:0100314" + ], + "cerebral inclusion bodies": [ + "HP:0100314" + ], + "lewy body": [ + "HP:0100315" + ], + "lewy bodies": [ + "HP:0100315" + ], + "lewy body disease": [ + "HP:0100315" + ], + "hirano body": [ + "HP:0100316" + ], + "hirano bodies": [ + "HP:0100316" + ], + "argyrophilic inclusion body": [ + "HP:0100317" + ], + "argyrophilic inclusion bodies": [ + "HP:0100317" + ], + "agyrophilic inclusion body": [ + "HP:0100317" + ], + "agyrophilic inclusion bodies": [ + "HP:0100317" + ], + "pick inclusion body": [ + "HP:0100317" + ], + "pick inclusion bodies": [ + "HP:0100317" + ], + "lafora body": [ + "HP:0100318" + ], + "lafora bodies": [ + "HP:0100318" + ], + "cerebral hyaline body": [ + "HP:0100319" + ], + "cerebral hyaline bodies": [ + "HP:0100319" + ], + "cerebral colloid body": [ + "HP:0100319" + ], + "cerebral colloid bodies": [ + "HP:0100319" + ], + "rosenthal fiber": [ + "HP:0100320" + ], + "rosenthal fibers": [ + "HP:0100320" + ], + "rosenthal fibre": [ + "HP:0100320" + ], + "rosenthal fibres": [ + "HP:0100320" + ], + "abnormal dentate nucleus morphology": [ + "HP:0100321" + ], + "abnormality of the dentate nucleus": [ + "HP:0100321" + ], + "aplasia of the pyramidal tract": [ + "HP:0100322" + ], + "absent pyramidal tract": [ + "HP:0100322" + ], + "juvenile aseptic necrosis": [ + "HP:0100323" + ], + "aseptic epiphyseal necrosis": [ + "HP:0100323" + ], + "scleroderma": [ + "HP:0100324" + ], + "progressive systemic scleroderma": [ + "HP:0100324" + ], + "pseudoscleroderma": [ + "HP:0100324" + ], + "immunologic hypersensitivity": [ + "HP:0100326" + ], + "cow milk allergy": [ + "HP:0100327" + ], + "ige - mediate cow milk allergy": [ + "HP:0100327" + ], + "ige - mediated cow milk allergy": [ + "HP:0100327" + ], + "immunoglobulin e - mediate cow milk allergy": [ + "HP:0100327" + ], + "immunoglobulin e - mediated cow milk allergy": [ + "HP:0100327" + ], + "milk allergy": [ + "HP:0100327" + ], + "carpometacarpal synostosis": [ + "HP:0100328" + ], + "fuse wrist bone and long bone of hand": [ + "HP:0100328" + ], + "fused wrist bones and long bones of hand": [ + "HP:0100328" + ], + "tarsometatarsal synostosis": [ + "HP:0100329" + ], + "fuse bone of the midfoot": [ + "HP:0100329" + ], + "fused bones of the midfoot": [ + "HP:0100329" + ], + "unilateral cleft lip": [ + "HP:0100333" + ], + "one side cleft upper lip": [ + "HP:0100333" + ], + "one sided cleft upper lip": [ + "HP:0100333" + ], + "unilateral cheiloschisis": [ + "HP:0100333" + ], + "unilateral cleft upper lip": [ + "HP:0100333" + ], + "unilateral cleft palate": [ + "HP:0100334" + ], + "one side cleft palate": [ + "HP:0100334" + ], + "one sided cleft palate": [ + "HP:0100334" + ], + "unilateral palatoschisis": [ + "HP:0100334" + ], + "non - midline cleft lip": [ + "HP:0100335" + ], + "non - midline cleft of the upper lip": [ + "HP:0100335" + ], + "paramedian cleft of the upper lip": [ + "HP:0100335" + ], + "bilateral cleft lip": [ + "HP:0100336" + ], + "bilateral cheiloschisis": [ + "HP:0100336" + ], + "both side cleft lip": [ + "HP:0100336" + ], + "both sided cleft lip": [ + "HP:0100336" + ], + "right and leave cleft lip": [ + "HP:0100336" + ], + "right and left cleft lip": [ + "HP:0100336" + ], + "bilateral cleft palate": [ + "HP:0100337" + ], + "bilateral palatoschisis": [ + "HP:0100337" + ], + "right and leave cleft palate": [ + "HP:0100337" + ], + "right and left cleft palate": [ + "HP:0100337" + ], + "non - midline cleft palate": [ + "HP:0100338" + ], + "paramedian cleft palate": [ + "HP:0100338" + ], + "abnormality of the o naviculare pedis": [ + "HP:0100339" + ], + "abnormality of the os naviculare pedis": [ + "HP:0100339" + ], + "fibular deviation of the 4th toe": [ + "HP:0100340" + ], + "tibial deviation of the 4th toe": [ + "HP:0100341" + ], + "fibular deviation of the 3rd toe": [ + "HP:0100342" + ], + "tibial deviation of the 3rd toe": [ + "HP:0100343" + ], + "fibular deviation of the 2nd toe": [ + "HP:0100344" + ], + "tibial deviation of the 2nd toe": [ + "HP:0100345" + ], + "fibular deviation of the 5th toe": [ + "HP:0100346" + ], + "tibial deviation of the 5th toe": [ + "HP:0100347" + ], + "contracture of the proximal interphalangeal joint of the 2nd toe": [ + "HP:0100348" + ], + "camptodactyly of the 2nd toe": [ + "HP:0100348" + ], + "camptodactyly of the second toe": [ + "HP:0100348" + ], + "contracture of the proximal interphalangeal joint of the 3rd toe": [ + "HP:0100349" + ], + "camptodactyly of the 3rd toe": [ + "HP:0100349" + ], + "contracture of the proximal interphalangeal joint of the 4th toe": [ + "HP:0100350" + ], + "camptodactyly of the 4th toe": [ + "HP:0100350" + ], + "camptodactyly of the fourth toe": [ + "HP:0100350" + ], + "contracture of the innermost hinge joint of the 4th toe": [ + "HP:0100350" + ], + "contracture of the proximal interphalangeal joint of the 5th toe": [ + "HP:0100351" + ], + "contractures of the proximal interphalangeal joint of the 5th toe": [ + "HP:0100351" + ], + "camptodactyly of the 5th toe": [ + "HP:0100351" + ], + "camptodactyly of the fifth toe": [ + "HP:0100351" + ], + "contracture of the distal interphalangeal joint of the 2nd toe": [ + "HP:0100352" + ], + "contracture of the distal interphalangeal joint of the second toe": [ + "HP:0100352" + ], + "contracture of the distal interphalangeal joint of the 3rd toe": [ + "HP:0100353" + ], + "contracture of the distal interphalangeal joint of the 4th toe": [ + "HP:0100354" + ], + "contracture of the distal interphalangeal joint of the 5th toe": [ + "HP:0100355" + ], + "contractures of the distal interphalangeal joint of the 5th toe": [ + "HP:0100355" + ], + "contracture of the outermost hinge joint of the 5th toe": [ + "HP:0100355" + ], + "contracture of the metatarsophalangeal joint of the 2nd toe": [ + "HP:0100356" + ], + "contracture of the metatarsophalangeal joint of the 3rd toe": [ + "HP:0100357" + ], + "contracture of the metatarsophalangeal joint of the 4th toe": [ + "HP:0100358" + ], + "contracture of the metatarsophalangeal joint of the 5th toe": [ + "HP:0100359" + ], + "contracture of the joint of the upper limb": [ + "HP:0100360" + ], + "contractures of the joints of the upper limbs": [ + "HP:0100360" + ], + "aplasia of the phalanx of the 3rd toe": [ + "HP:0100362" + ], + "aplasia of the phalanges of the 3rd toe": [ + "HP:0100362" + ], + "absent digital bone of the 3rd toe": [ + "HP:0100362" + ], + "aplasia of the phalanx of the 4th toe": [ + "HP:0100363" + ], + "aplasia of the phalanges of the 4th toe": [ + "HP:0100363" + ], + "absent bone of the 4th toe": [ + "HP:0100363" + ], + "absent bones of the 4th toe": [ + "HP:0100363" + ], + "aplasia of the phalanx of the 5th toe": [ + "HP:0100364" + ], + "aplasia of the phalanges of the 5th toe": [ + "HP:0100364" + ], + "absent little toe bone": [ + "HP:0100364" + ], + "absent little toe bones": [ + "HP:0100364" + ], + "absent pinkie toe bone": [ + "HP:0100364" + ], + "absent pinkie toe bones": [ + "HP:0100364" + ], + "absent pinky toe bone": [ + "HP:0100364" + ], + "absent pinky toe bones": [ + "HP:0100364" + ], + "short phalanx of the 3rd toe": [ + "HP:0100366" + ], + "hypoplastic / small phalanx of the 3rd toe": [ + "HP:0100366" + ], + "hypoplastic / small phalanges of the 3rd toe": [ + "HP:0100366" + ], + "short 3rd toe bone": [ + "HP:0100366" + ], + "short phalanx of the third toe": [ + "HP:0100366" + ], + "short phalanx of the 4th toe": [ + "HP:0100367" + ], + "hypoplastic / small phalanx of the 4th toe": [ + "HP:0100367" + ], + "hypoplastic / small phalanges of the 4th toe": [ + "HP:0100367" + ], + "short 4th toe bone": [ + "HP:0100367" + ], + "short phalanx of the fourth toe": [ + "HP:0100367" + ], + "short phalanx of the 5th toe": [ + "HP:0100368" + ], + "hypoplastic / small phalanx of the 5th toe": [ + "HP:0100368" + ], + "hypoplastic / small phalanges of the 5th toe": [ + "HP:0100368" + ], + "short little toe bone": [ + "HP:0100368" + ], + "short phalanx of the fifth toe": [ + "HP:0100368" + ], + "short pinkie toe bone": [ + "HP:0100368" + ], + "short pinky toe bone": [ + "HP:0100368" + ], + "aplasia / hypoplasia of the distal phalanx of the 3rd toe": [ + "HP:0100369" + ], + "absent / small outermost 3rd toe bone": [ + "HP:0100369" + ], + "absent / underdevelop outermost 3rd toe bone": [ + "HP:0100369" + ], + "absent / underdeveloped outermost 3rd toe bone": [ + "HP:0100369" + ], + "aplasia / hypoplasia of the distal phalanx of the 4th toe": [ + "HP:0100370" + ], + "absent / small outermost bone of 4th toe": [ + "HP:0100370" + ], + "absent / underdevelop outermost bone of 4th toe": [ + "HP:0100370" + ], + "absent / underdeveloped outermost bone of 4th toe": [ + "HP:0100370" + ], + "aplasia / hypoplasia of the distal phalanx of the 5th toe": [ + "HP:0100371" + ], + "absent / small outermost little toe bone": [ + "HP:0100371" + ], + "absent / small outermost pinkie toe bone": [ + "HP:0100371" + ], + "absent / small outermost pinky toe bone": [ + "HP:0100371" + ], + "absent / underdevelop outermost pinky toe bone": [ + "HP:0100371" + ], + "absent / underdeveloped outermost pinky toe bone": [ + "HP:0100371" + ], + "aplasia / hypoplasia of the middle phalanx of the 3rd toe": [ + "HP:0100372" + ], + "absent / small middle 3rd toe bone": [ + "HP:0100372" + ], + "absent / underdevelop middle 3rd toe bone": [ + "HP:0100372" + ], + "absent / underdeveloped middle 3rd toe bone": [ + "HP:0100372" + ], + "aplasia / hypoplasia of the middle phalanx of the 4th toe": [ + "HP:0100373" + ], + "absent / small middle bone of the 4th toe": [ + "HP:0100373" + ], + "absent / underdevelop middle bone of the 4th toe": [ + "HP:0100373" + ], + "absent / underdeveloped middle bone of the 4th toe": [ + "HP:0100373" + ], + "aplasia / hypoplasia of the middle phalanx of the 5th toe": [ + "HP:0100374" + ], + "absent / small middle 5th toe bone": [ + "HP:0100374" + ], + "absent / underdevelop middle bone of little toe": [ + "HP:0100374" + ], + "absent / underdeveloped middle bone of little toe": [ + "HP:0100374" + ], + "absent / underdevelop middle bone of pinkie toe": [ + "HP:0100374" + ], + "absent / underdeveloped middle bone of pinkie toe": [ + "HP:0100374" + ], + "absent / underdevelop middle bone of pinky toe": [ + "HP:0100374" + ], + "absent / underdeveloped middle bone of pinky toe": [ + "HP:0100374" + ], + "aplasia / hypoplasia of the proximal phalanx of the 3rd toe": [ + "HP:0100375" + ], + "absent / small innermost bone of 3rd toe": [ + "HP:0100375" + ], + "absent / underdevelop innermost bone of 3rd toe": [ + "HP:0100375" + ], + "absent / underdeveloped innermost bone of 3rd toe": [ + "HP:0100375" + ], + "aplasia / hypoplasia of the proximal phalanx of the 4th toe": [ + "HP:0100376" + ], + "absent / small innermost 4th toe bone": [ + "HP:0100376" + ], + "absent / underdevelop innermost 4th toe bone": [ + "HP:0100376" + ], + "absent / underdeveloped innermost 4th toe bone": [ + "HP:0100376" + ], + "aplasia / hypoplasia of the proximal phalanx of the 5th toe": [ + "HP:0100377" + ], + "absent / small innermost little toe bone": [ + "HP:0100377" + ], + "absent / small innermost pinkie toe bone": [ + "HP:0100377" + ], + "absent / small innermost pinky toe bone": [ + "HP:0100377" + ], + "absent / underdevelop innermost 5th toe bone": [ + "HP:0100377" + ], + "absent / underdeveloped innermost 5th toe bone": [ + "HP:0100377" + ], + "absent distal phalanx of the 3rd toe": [ + "HP:0100378" + ], + "absent distal phalanx of the third toe": [ + "HP:0100378" + ], + "absent outermost bone of the 3rd toe": [ + "HP:0100378" + ], + "aplasia of the distal phalanx of the 3rd toe": [ + "HP:0100378" + ], + "aplasia of the distal phalanx of the 4th toe": [ + "HP:0100379" + ], + "absent distal phalanx of the 4th toe": [ + "HP:0100379" + ], + "absent outermost bone of the 4th toe": [ + "HP:0100379" + ], + "aplasia of the distal phalanx of the 5th toe": [ + "HP:0100380" + ], + "absent outermost bone of the little toe": [ + "HP:0100380" + ], + "absent outermost bone of the pinkie toe": [ + "HP:0100380" + ], + "absent outermost bone of the pinky toe": [ + "HP:0100380" + ], + "absent middle phalanx of the 3rd toe": [ + "HP:0100381" + ], + "absent middle bone of the 3rd toe": [ + "HP:0100381" + ], + "absent middle phalanx of the third toe": [ + "HP:0100381" + ], + "aplasia of the middle phalanx of the 3rd toe": [ + "HP:0100381" + ], + "aplasia of the middle phalanx of the 4th toe": [ + "HP:0100382" + ], + "absent middle bone of 4th toe": [ + "HP:0100382" + ], + "aplasia of the middle phalanx of the 5th toe": [ + "HP:0100383" + ], + "absent middle bone of little toe": [ + "HP:0100383" + ], + "absent middle bone of pinkie toe": [ + "HP:0100383" + ], + "absent middle bone of pinky toe": [ + "HP:0100383" + ], + "absent proximal phalanx of the 3rd toe": [ + "HP:0100384" + ], + "absent innermost bone of the 3rd toe": [ + "HP:0100384" + ], + "aplasia of the proximal phalanx of the 3rd toe": [ + "HP:0100384" + ], + "aplasia of the proximal phalanx of the 4th toe": [ + "HP:0100385" + ], + "absent innermost bone of the 4th toe": [ + "HP:0100385" + ], + "aplasia of the proximal phalanx of the 5th toe": [ + "HP:0100386" + ], + "absent innermost bone of the little toe": [ + "HP:0100386" + ], + "absent innermost bone of the pinkie toe": [ + "HP:0100386" + ], + "absent innermost bone of the pinky toe": [ + "HP:0100386" + ], + "aplasia of the middle phalanx of the toe": [ + "HP:0100387" + ], + "aplasia of the middle phalanges of the toes": [ + "HP:0100387" + ], + "absent middle toe bone": [ + "HP:0100387" + ], + "absent middle toe bones": [ + "HP:0100387" + ], + "aplasia of the proximal phalanx of the toe": [ + "HP:0100388" + ], + "aplasia of the proximal phalanges of the toes": [ + "HP:0100388" + ], + "absent innermost toe bone": [ + "HP:0100388" + ], + "absent innermost toe bones": [ + "HP:0100388" + ], + "short distal phalanx of the 3rd toe": [ + "HP:0100389" + ], + "hypoplastic / small distal phalanx of the 3rd toe": [ + "HP:0100389" + ], + "short distal phalanx of the third toe": [ + "HP:0100389" + ], + "short outermost bone of the 3rd toe": [ + "HP:0100389" + ], + "short distal phalanx of the 4th toe": [ + "HP:0100390" + ], + "hypoplastic / small distal phalanx of the 4th toe": [ + "HP:0100390" + ], + "short distal phalanx of the fourth toe": [ + "HP:0100390" + ], + "short outermost bone of the 4th toe": [ + "HP:0100390" + ], + "short distal phalanx of the 5th toe": [ + "HP:0100391" + ], + "hypoplastic / small distal phalanx of the 5th toe": [ + "HP:0100391" + ], + "short distal phalanx of the fifth toe": [ + "HP:0100391" + ], + "short outermost bone of the little toe": [ + "HP:0100391" + ], + "short outermost bone of the pinkie toe": [ + "HP:0100391" + ], + "short outermost bone of the pinky toe": [ + "HP:0100391" + ], + "short middle phalanx of the 3rd toe": [ + "HP:0100392" + ], + "hypoplastic / small middle phalanx of the 3rd toe": [ + "HP:0100392" + ], + "short middle phalanx of the third toe": [ + "HP:0100392" + ], + "short middle phalanx of the 4th toe": [ + "HP:0100393" + ], + "hypoplastic / small middle phalanx of the 4th toe": [ + "HP:0100393" + ], + "short middle bone of 4th toe": [ + "HP:0100393" + ], + "short middle phalanx of the fourth toe": [ + "HP:0100393" + ], + "short middle phalanx of the 5th toe": [ + "HP:0100394" + ], + "hypoplastic / small middle phalanx of the 5th toe": [ + "HP:0100394" + ], + "short middle bone of little toe": [ + "HP:0100394" + ], + "short middle bone of pinkie toe": [ + "HP:0100394" + ], + "short middle bone of pinky toe": [ + "HP:0100394" + ], + "short middle phalanx of the fifth toe": [ + "HP:0100394" + ], + "short proximal phalanx of the 3rd toe": [ + "HP:0100395" + ], + "hypoplastic / small proximal phalanx of the 3rd toe": [ + "HP:0100395" + ], + "short proximal phalanx of the third toe": [ + "HP:0100395" + ], + "short proximal phalanx of the 4th toe": [ + "HP:0100396" + ], + "hypoplastic / small proximal phalanx of the 4th toe": [ + "HP:0100396" + ], + "short fourth toe proximal phalanx": [ + "HP:0100396" + ], + "short proximal phalanx of the fourth toe": [ + "HP:0100396" + ], + "short proximal phalanx of the 5th toe": [ + "HP:0100397" + ], + "hypoplastic / small proximal phalanx of the 5th toe": [ + "HP:0100397" + ], + "short innermost bone of little toe": [ + "HP:0100397" + ], + "short innermost bone of pinkie toe": [ + "HP:0100397" + ], + "short innermost bone of pinky toe": [ + "HP:0100397" + ], + "short proximal phalanx of the fifth toe": [ + "HP:0100397" + ], + "duplication of the distal phalanx of the 3rd toe": [ + "HP:0100398" + ], + "duplication of the distal phalanx of the third toe": [ + "HP:0100398" + ], + "duplication of the outermost bone of the 3rd toe": [ + "HP:0100398" + ], + "partial / complete duplication of the distal phalanx of the 3rd toe": [ + "HP:0100398" + ], + "duplication of the distal phalanx of the 4th toe": [ + "HP:0100399" + ], + "duplication of the distal phalanx of the fourth toe": [ + "HP:0100399" + ], + "duplication of the outermost bone of the 4th toe": [ + "HP:0100399" + ], + "partial / complete duplication of the distal phalanx of the 4th toe": [ + "HP:0100399" + ], + "duplication of the distal phalanx of the 5th toe": [ + "HP:0100400" + ], + "duplication of the distal phalanx of the fifth toe": [ + "HP:0100400" + ], + "duplication of the outermost bone of the fifth toe": [ + "HP:0100400" + ], + "duplication of the outermost bone of the little toe": [ + "HP:0100400" + ], + "duplication of the outermost bone of the pinkie toe": [ + "HP:0100400" + ], + "duplication of the outermost bone of the pinky toe": [ + "HP:0100400" + ], + "partial / complete duplication of the distal phalanx of the 5th toe": [ + "HP:0100400" + ], + "duplication of the middle phalanx of the 3rd toe": [ + "HP:0100401" + ], + "duplication of the middle bone of the 3rd toe": [ + "HP:0100401" + ], + "duplication of the middle phalanx of the third toe": [ + "HP:0100401" + ], + "partial / complete duplication of the middle phalanx of the 3rd toe": [ + "HP:0100401" + ], + "duplication of the middle phalanx of the 4th toe": [ + "HP:0100402" + ], + "duplication of the middle bone of the 4th toe": [ + "HP:0100402" + ], + "duplication of the middle phalanx of the fourth toe": [ + "HP:0100402" + ], + "partial / complete duplication of the middle phalanx of the 4th toe": [ + "HP:0100402" + ], + "duplication of the middle phalanx of the 5th toe": [ + "HP:0100403" + ], + "duplication of the middle bone of the little toe": [ + "HP:0100403" + ], + "duplication of the middle bone of the pinkie toe": [ + "HP:0100403" + ], + "duplication of the middle bone of the pinky toe": [ + "HP:0100403" + ], + "duplication of the middle phalanx of the fifth toe": [ + "HP:0100403" + ], + "partial / complete duplication of the middle phalanx of the 5th toe": [ + "HP:0100403" + ], + "duplication of the proximal phalanx of the 3rd toe": [ + "HP:0100404" + ], + "duplication of the innermost 3rd toe bone": [ + "HP:0100404" + ], + "duplication of the proximal phalanx of the third toe": [ + "HP:0100404" + ], + "partial / complete duplication of the proximal phalanx of the 3rd toe": [ + "HP:0100404" + ], + "duplication of the proximal phalanx of the 4th toe": [ + "HP:0100405" + ], + "duplication of the innermost 4th toe bone": [ + "HP:0100405" + ], + "duplication of the proximal phalanx of the fourth toe": [ + "HP:0100405" + ], + "partial / complete duplication of the proximal phalanx of the 4th toe": [ + "HP:0100405" + ], + "duplication of the proximal phalanx of the 5th toe": [ + "HP:0100406" + ], + "duplication of the innermost bone of the little toe": [ + "HP:0100406" + ], + "duplication of the innermost bone of the pinkie toe": [ + "HP:0100406" + ], + "duplication of the innermost bone of the pinky toe": [ + "HP:0100406" + ], + "duplication of the proximal phalanx of the fifth toe": [ + "HP:0100406" + ], + "partial / complete duplication of the proximal phalanx of the 5th toe": [ + "HP:0100406" + ], + "complete duplication of the distal phalanx of the 3rd toe": [ + "HP:0100407" + ], + "complete duplication of the distal phalanx of the third toe": [ + "HP:0100407" + ], + "complete duplication of the outermost bone of the 3rd toe": [ + "HP:0100407" + ], + "complete duplication of the distal phalanx of the 4th toe": [ + "HP:0100408" + ], + "complete duplication of the distal phalanx of the fourth toe": [ + "HP:0100408" + ], + "complete duplication of the outermost bone of the 4th toe": [ + "HP:0100408" + ], + "complete duplication of the distal phalanx of the 5th toe": [ + "HP:0100409" + ], + "complete duplication of the distal phalanx of the fifth toe": [ + "HP:0100409" + ], + "complete duplication of the outermost bone of the little toe": [ + "HP:0100409" + ], + "complete duplication of the outermost bone of the pinkie toe": [ + "HP:0100409" + ], + "complete duplication of the outermost bone of the pinky toe": [ + "HP:0100409" + ], + "complete duplication of the middle phalanx of the 3rd toe": [ + "HP:0100410" + ], + "complete duplication of the middle bone of the 3rd toe": [ + "HP:0100410" + ], + "complete duplication of the middle 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"uneven increase in bone density in the outermost bone of the 4th toe": [ + "HP:0100468" + ], + "patchy sclerosis of the distal phalanx of the 5th toe": [ + "HP:0100469" + ], + "uneven increase in bone density in the outermost little toe bone": [ + "HP:0100469" + ], + "uneven increase in bone density in the outermost pinkie toe bone": [ + "HP:0100469" + ], + "uneven increase in bone density in the outermost pinky toe bone": [ + "HP:0100469" + ], + "symphalangism affect the middle phalanx of the 3rd toe": [ + "HP:0100470" + ], + "symphalangism affecting the middle phalanx of the 3rd toe": [ + "HP:0100470" + ], + "fuse middle bone of 3rd toe": [ + "HP:0100470" + ], + "fused middle bones of 3rd toe": [ + "HP:0100470" + ], + "symphalangism affect the middle phalanx of the 4th toe": [ + "HP:0100471" + ], + "symphalangism affecting the middle phalanx of the 4th toe": [ + "HP:0100471" + ], + "fuse middle bone of 4th toe": [ + "HP:0100471" + ], + "fused middle bones of 4th toe": [ + 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[ + "HP:0100481" + ], + "fuse innermost and middle bone of 4th toe": [ + "HP:0100481" + ], + "fused innermost and middle bones of 4th toe": [ + "HP:0100481" + ], + "symphalangism of the middle and proximal phalanx of the 4th toe": [ + "HP:0100481" + ], + "symphalangism of the middle and proximal phalanges of the 4th toe": [ + "HP:0100481" + ], + "proximal / middle symphalangism of 5th toe": [ + "HP:0100482" + ], + "fuse innermost and middle little toe bone": [ + "HP:0100482" + ], + "fused innermost and middle little toe bones": [ + "HP:0100482" + ], + "fuse innermost and middle pinkie toe bone": [ + "HP:0100482" + ], + "fused innermost and middle pinkie toe bones": [ + "HP:0100482" + ], + "fuse innermost and middle pinky toe bone": [ + "HP:0100482" + ], + "fused innermost and middle pinky toe bones": [ + "HP:0100482" + ], + "symphalangism of the middle and proximal phalanx of the 5th toe": [ + "HP:0100482" + ], + "symphalangism of the middle and proximal phalanges of the 5th toe": [ + "HP:0100482" + ], + "symphalangism of the proximal phalanx of the 2nd toe with the 2nd metatarsal": [ + "HP:0100483" + ], + "fuse innermost bone of 2nd toe with the 2nd long bone of foot": [ + "HP:0100483" + ], + "fused innermost bone of 2nd toe with the 2nd long bone of foot": [ + "HP:0100483" + ], + "symphalangism of the proximal phalanx of the 3rd toe with the 3rd metatarsal": [ + "HP:0100484" + ], + "fuse innermost bone of third toe with 3rd long bone of foot": [ + "HP:0100484" + ], + "fused innermost bones of third toe with 3rd long bone of foot": [ + "HP:0100484" + ], + "symphalangism of the proximal phalanx of the 4th toe with the 4th metatarsal": [ + "HP:0100485" + ], + "fuse innermost bone of the 4th toe with 4th long bone of foot": [ + "HP:0100485" + ], + "fused innermost bone of the 4th toe with 4th long bone of foot": [ + "HP:0100485" + ], + "symphalangism of the proximal phalanx of the 5th toe with the 5th metatarsal": [ + "HP:0100486" + ], + "fuse innermost pinky toe bone with the 5th long bone of foot": [ + "HP:0100486" + ], + "fused innermost pinky toe bone with the 5th long bone of foot": [ + "HP:0100486" + ], + "triangular shape distal phalanx of the 5th toe": [ + "HP:0100487" + ], + "triangular shaped distal phalanx of the 5th toe": [ + "HP:0100487" + ], + "triangular shape outermost bone of the little toe": [ + "HP:0100487" + ], + "triangular shaped outermost bone of the little toe": [ + "HP:0100487" + ], + "triangular shape outermost bone of the pinkie toe": [ + "HP:0100487" + ], + "triangular shaped outermost bone of the pinkie toe": [ + "HP:0100487" + ], + "triangular shape outermost bone of the pinky toe": [ + "HP:0100487" + ], + "triangular shaped outermost bone of the pinky toe": [ + "HP:0100487" + ], + "synostosis of the proximal phalanx of the hallux with the 1st metatarsal": [ + "HP:0100488" + ], + "fusion of the innermost big toe bone with the 1st long bone of foot": [ + "HP:0100488" + ], + "proximal / middle symphalangism of 2nd toe": [ + "HP:0100489" + ], + "fuse middle and innermost bone of 2nd toe": [ + "HP:0100489" + ], + "fused middle and innermost bones of 2nd toe": [ + "HP:0100489" + ], + "symphalangism of the middle and proximal phalanx of the 2nd toe": [ + "HP:0100489" + ], + "symphalangism of the middle and proximal phalanges of the 2nd toe": [ + "HP:0100489" + ], + "camptodactyly of finger": [ + "HP:0100490" + ], + "camptodactyly of hand": [ + "HP:0100490" + ], + "camptodactyly of hands": [ + "HP:0100490" + ], + "camptodactyly of proximal interphalangeal joint": [ + "HP:0100490" + ], + "contracture of the proximal interphalangeal joint of the finger": [ + "HP:0100490" + ], + "contractures of the proximal interphalangeal joints of the fingers": [ + "HP:0100490" + ], + "flexion contracture of proximal interphalangeal joint": [ + "HP:0100490" + ], + "flexion contractures of proximal interphalangeal joints": [ + "HP:0100490" + ], + "permanent flexion of the finger": [ + "HP:0100490" + ], + "proximal interphalangeal finger joint contracture": [ + "HP:0100490" + ], + "proximal interphalangeal finger joint contractures": [ + "HP:0100490" + ], + "abnormality of low limb joint": [ + "HP:0100491" + ], + "abnormality of lower limb joint": [ + "HP:0100491" + ], + "abnormality of the joint of the low limb": [ + "HP:0100491" + ], + "abnormality of the joints of the lower limbs": [ + "HP:0100491" + ], + "joint contracture involve the joint of the foot": [ + "HP:0100492" + ], + "joint contractures involving the joints of the feet": [ + "HP:0100492" + ], + "hypoammonemia": [ + "HP:0100493" + ], + "abnormal mast cell morphology": [ + "HP:0100494" + ], + "abnormality of mast cell": [ + "HP:0100494" + ], + "abnormality of mast cells": [ + "HP:0100494" + ], + "abnormality of mastocyte": [ + "HP:0100494" + ], + "abnormality of mastocytes": [ + "HP:0100494" + ], + "mastocytosis": [ + "HP:0100495" + ], + "abnormality of the vitamin b3 metabolism": [ + "HP:0100496" + ], + "vitamin b3 deficiency": [ + "HP:0100497" + ], + "deviation of toe": [ + "HP:0100498" + ], + "deviation of toes": [ + "HP:0100498" + ], + "tibial deviation of toe": [ + "HP:0100499" + ], + "tibial deviation of toes": [ + "HP:0100499" + ], + "medial deviation of toe": [ + "HP:0100499" + ], + "medial deviation of toes": [ + "HP:0100499" + ], + "fibular deviation of toe": [ + "HP:0100500" + ], + "fibular deviation of toes": [ + "HP:0100500" + ], + "lateral deviation of toe": [ + "HP:0100500" + ], + "lateral deviation of toes": [ + "HP:0100500" + ], + "recurrent bronchiolitis": [ + "HP:0100501" + ], + "vitamin b12 deficiency": [ + "HP:0100502" + ], + "low level of vitamin b1": [ + "HP:0100503" + ], + "low levels of vitamin b1": [ + "HP:0100503" + ], + "reduce blood thiamine level": [ + "HP:0100503" + ], + "reduced blood thiamine level": [ + "HP:0100503" + ], + "vitamin b1 deficiency": [ + "HP:0100503" + ], + "low level of vitamin b2": [ + "HP:0100504" + ], + "low levels of vitamin b2": [ + "HP:0100504" + ], + "riboflavin deficiency": [ + "HP:0100504" + ], + "vitamin b2 deficiency": [ + "HP:0100504" + ], + "low level of vitamin b5": [ + "HP:0100505" + ], + "low levels of vitamin b5": [ + "HP:0100505" + ], + "vitamin b5 deficiency": [ + "HP:0100505" + ], + "low level of vitamin b8": [ + "HP:0100506" + ], + "low levels of vitamin b8": [ + "HP:0100506" + ], + "vitamin b8 deficiency": [ + "HP:0100506" + ], + "reduce blood folate concentration": [ + "HP:0100507" + ], + "reduced blood folate concentration": [ + "HP:0100507" + ], + "folate deficiency": [ + "HP:0100507" + ], + "vitamin b9 deficiency": [ + "HP:0100507" + ], + "abnormality of vitamin metabolism": [ + "HP:0100508" + ], + "abnormality of vitamin c metabolism": [ + "HP:0100509" + ], + "low level of vitamin c": [ + "HP:0100510" + ], + "low levels of vitamin c": [ + "HP:0100510" + ], + "vitamin c deficiency": [ + "HP:0100510" + ], + "abnormality of vitamin d metabolism": [ + "HP:0100511" + ], + "low level of vitamin d": [ + "HP:0100512" + ], + "low levels of vitamin d": [ + "HP:0100512" + ], + "deficient in vitamin d": [ + "HP:0100512" + ], + "vitamin d deficiency": [ + "HP:0100512" + ], + "low level of vitamin e": [ + "HP:0100513" + ], + "low levels of vitamin e": [ + "HP:0100513" + ], + "alpha - tocopherol deficiency": [ + "HP:0100513" + ], + "vitamin e deficiency": [ + "HP:0100513" + ], + "abnormality of vitamin e metabolism": [ + "HP:0100514" + ], + "pollakisuria": [ + "HP:0100515" + ], + "constant urination": [ + "HP:0100515" + ], + "frequent urination": [ + "HP:0100515" + ], + "neoplasm of the ureter": [ + "HP:0100516" + ], + "neoplasia of the ureter": [ + "HP:0100516" + ], + "neoplasia of the ureters": [ + "HP:0100516" + ], + "ureter , cancer of": [ + "HP:0100516" + ], + "neoplasm of the urethra": [ + "HP:0100517" + ], + "neoplasia of the urethra": [ + "HP:0100517" + ], + "dysuria": [ + "HP:0100518" + ], + "dull burning sensation with urination": [ + "HP:0100518" + ], + "painful or difficult urination": [ + "HP:0100518" + ], + "anuria": [ + "HP:0100519" + ], + "absent urine output": [ + "HP:0100519" + ], + "oliguria": [ + "HP:0100520" + ], + "neoplasm of the thymus": [ + "HP:0100521" + ], + "thymoma": [ + "HP:0100522" + ], + "liver abscess": [ + "HP:0100523" + ], + "hepatic abscess": [ + "HP:0100523" + ], + "limb duplication": [ + "HP:0100524" + ], + "dimelia": [ + "HP:0100524" + ], + "urachus fistula": [ + "HP:0100525" + ], + "neoplasm of the lung": [ + "HP:0100526" + ], + "lung cancer": [ + "HP:0100526" + ], + "lung tumor": [ + "HP:0100526" + ], + "lung tumour": [ + "HP:0100526" + ], + "neoplasia of the pleura": [ + "HP:0100527" + ], + "pleuropulmonary blastoma": [ + "HP:0100528" + ], + "abnormal blood phosphate concentration": [ + "HP:0100529" + ], + "abnormality of phosphate homeostasis": [ + "HP:0100529" + ], + "abnormal calcium - phosphate regulate hormone level": [ + "HP:0100530" + ], + "abnormal calcium - phosphate regulating hormone level": [ + "HP:0100530" + ], + "abnormal ca - phos regulate hormone level": [ + "HP:0100530" + ], + "abnormal ca - phos regulating hormone level": [ + "HP:0100530" + ], + "abnormal ca2+ po4 regulate hormone level": [ + "HP:0100530" + ], + "abnormal ca2+ po4 regulating hormone level": [ + "HP:0100530" + ], + "wind - swept deformity of the knee": [ + "HP:0100531" + ], + "wind - swept deformity of the knees": [ + "HP:0100531" + ], + "scleritis": [ + "HP:0100532" + ], + "inflammation of the outer white part of the eye": [ + "HP:0100532" + ], + "inflammatory abnormality of the eye": [ + "HP:0100533" + ], + "ocular inflammation": [ + "HP:0100533" + ], + "episcleritis": [ + "HP:0100534" + ], + "inflammation of the thin layer on top of the white part of eye": [ + "HP:0100534" + ], + "tibiofibular diastasis": [ + "HP:0100535" + ], + "abnormality of the fascia": [ + "HP:0100536" + ], + "fasciitis": [ + "HP:0100537" + ], + "inflammation of the fascia": [ + "HP:0100537" + ], + "abnormality of the supraorbital ridge": [ + "HP:0100538" + ], + "abnormality of the supraorbital ridges": [ + "HP:0100538" + ], + "abnormality of the brow of the face": [ + "HP:0100538" + ], + "deformity of the supraorbital margin": [ + "HP:0100538" + ], + "deformity of the supraorbital margins": [ + "HP:0100538" + ], + "deformity of the supraorbital ridge": [ + "HP:0100538" + ], + "deformity of the supraorbital ridges": [ + "HP:0100538" + ], + "malformation of the supraorbital margin": [ + "HP:0100538" + ], + "malformation of the supraorbital margins": [ + "HP:0100538" + ], + "malformation of the supraorbital ridge": [ + "HP:0100538" + ], + "malformation of the supraorbital ridges": [ + "HP:0100538" + ], + "periorbital edema": [ + "HP:0100539" + ], + "periorbital cellulitis": [ + "HP:0100539" + ], + "periorbital oedema": [ + "HP:0100539" + ], + "palpebral edema": [ + "HP:0100540" + ], + "edema of the eyelid": [ + "HP:0100540" + ], + "edema of the eyelids": [ + "HP:0100540" + ], + "eyelid edema": [ + "HP:0100540" + ], + "eyelid oedema": [ + "HP:0100540" + ], + "fullness of eyelid": [ + "HP:0100540" + ], + "fullness of eyelids": [ + "HP:0100540" + ], + "oedema of the eyelid": [ + "HP:0100540" + ], + "oedema of the eyelids": [ + "HP:0100540" + ], + "palpebral oedema": [ + "HP:0100540" + ], + "puffy eyelid": [ + "HP:0100540" + ], + "puffy eyelids": [ + "HP:0100540" + ], + "puffy lid": [ + "HP:0100540" + ], + "puffy lids": [ + "HP:0100540" + ], + "swell of eyelid": [ + "HP:0100540" + ], + "swelling of eyelids": [ + "HP:0100540" + ], + "femoral hernia": [ + "HP:0100541" + ], + "crural hernia": [ + "HP:0100541" + ], + "abnormal localization of kidney": [ + "HP:0100542" + ], + "abnormal localisation of kidney": [ + "HP:0100542" + ], + "abnormal localisation of kidneys": [ + "HP:0100542" + ], + "cognitive impairment": [ + "HP:0100543" + ], + "abnormality of cognition": [ + "HP:0100543" + ], + "cognitive abnormality": [ + "HP:0100543" + ], + "cognitive defect": [ + "HP:0100543" + ], + "cognitive defects": [ + "HP:0100543" + ], + "cognitive deficit": [ + "HP:0100543" + ], + "cognitive deficits": [ + "HP:0100543" + ], + "intellectual impairment": [ + "HP:0100543" + ], + "neoplasm of the heart": [ + "HP:0100544" + ], + "cardiac neoplasia": [ + "HP:0100544" + ], + "cardiac neoplasm": [ + "HP:0100544" + ], + "heart tumor": [ + "HP:0100544" + ], + "heart tumour": [ + "HP:0100544" + ], + "arterial stenosis": [ + "HP:0100545" + ], + "narrowing of an artery": [ + "HP:0100545" + ], + "carotid artery stenosis": [ + "HP:0100546" + ], + "carotid stenosis": [ + "HP:0100546" + ], + "narrowing of carotid artery": [ + "HP:0100546" + ], + "abnormality of forebrain morphology": [ + "HP:0100547" + ], + "abnormal shape of forebrain": [ + "HP:0100547" + ], + "abnormality of the forebrain": [ + "HP:0100547" + ], + "exstrophy": [ + "HP:0100548" + ], + "tendon rupture": [ + "HP:0100550" + ], + "rupture of tendon": [ + "HP:0100550" + ], + "rupture of tendons": [ + "HP:0100550" + ], + "rupture tendon": [ + "HP:0100550" + ], + "ruptured tendon": [ + "HP:0100550" + ], + "tendon / muscle rupture": [ + "HP:0100550" + ], + "neoplasm of the trachea": [ + "HP:0100551" + ], + "tracheal neoplasm": [ + "HP:0100551" + ], + "neoplasm of the tracheobronchial system": [ + "HP:0100552" + ], + "hemihypertrophy of low limb": [ + "HP:0100553" + ], + "hemihypertrophy of lower limb": [ + "HP:0100553" + ], + "overgrowth of one leg": [ + "HP:0100553" + ], + "hemihypertrophy of upper limb": [ + "HP:0100554" + ], + "overgrowth of one arm": [ + "HP:0100554" + ], + "asymmetric growth": [ + "HP:0100555" + ], + "uneven or disproportionate growth of one body part compare to another": [ + "HP:0100555" + ], + "uneven or disproportionate growth of one body part compared to another": [ + "HP:0100555" + ], + "hemiatrophy": [ + "HP:0100556" + ], + "asymmetric limb shorten": [ + "HP:0100556" + ], + "asymmetric limb shortening": [ + "HP:0100556" + ], + "hemiatrophy of the body": [ + "HP:0100556" + ], + "hemiatrophy of low limb": [ + "HP:0100557" + ], + "hemiatrophy of lower limb": [ + "HP:0100557" + ], + "asymmetric low limb shorten": [ + "HP:0100557" + ], + "asymmetric lower limb shortening": [ + "HP:0100557" + ], + "hemiatrophy of upper limb": [ + "HP:0100558" + ], + "asymmetric upper limb shorten": [ + "HP:0100558" + ], + "asymmetric upper limb shortening": [ + "HP:0100558" + ], + "hemihypotrophy of upper limb": [ + "HP:0100558" + ], + "low limb asymmetry": [ + "HP:0100559" + ], + "lower limb asymmetry": [ + "HP:0100559" + ], + "left and right leg differ in length or width": [ + "HP:0100559" + ], + "leg length discrepancy": [ + "HP:0100559" + ], + "upper limb asymmetry": [ + "HP:0100560" + ], + "unequal size of arm": [ + "HP:0100560" + ], + "unequal size of arms": [ + "HP:0100560" + ], + "spinal cord lesion": [ + "HP:0100561" + ], + "diplomyelia": [ + "HP:0100562" + ], + "duplication of spinal cord": [ + "HP:0100562" + ], + "diastomatomyelia": [ + "HP:0100563" + ], + "triplomyelia": [ + "HP:0100564" + ], + "triplication of spinal cord": [ + "HP:0100564" + ], + "hydromyelia": [ + "HP:0100565" + ], + "amyelia": [ + "HP:0100566" + ], + "absent spinal cord": [ + "HP:0100566" + ], + "neoplasm of the endocrine system": [ + "HP:0100568" + ], + "endocrine neoplasia": [ + "HP:0100568" + ], + "abnormally ossify vertebra": [ + "HP:0100569" + ], + "abnormally ossified vertebrae": [ + "HP:0100569" + ], + "abnormal bone maturation of vertebra": [ + "HP:0100569" + ], + "abnormal vertebral ossification": [ + "HP:0100569" + ], + "abnormality of ossification / mineralisation of vertebra": [ + "HP:0100569" + ], + "abnormality of ossification / mineralisation of vertebrae": [ + "HP:0100569" + ], + "carcinoid tumor": [ + "HP:0100570" + ], + "carcinoid": [ + "HP:0100570" + ], + "carcinoid tumors": [ + "HP:0100570" + ], + "carcinoid tumour": [ + "HP:0100570" + ], + "carcinoid tumours": [ + "HP:0100570" + ], + "cardiac diverticulum": [ + "HP:0100571" + ], + "ventricular diverticulum": [ + "HP:0100571" + ], + "fibrous cardiac diverticulum": [ + "HP:0100572" + ], + "congenital ventricular aneurysm": [ + "HP:0100572" + ], + "muscular cardiac diverticulum": [ + "HP:0100573" + ], + "biliary tract neoplasm": [ + "HP:0100574" + ], + "neoplasia of the biliary tract": [ + "HP:0100574" + ], + "neoplasm of the gallbladder": [ + "HP:0100575" + ], + "neoplasia of the gallbladder": [ + "HP:0100575" + ], + "amaurosis fugax": [ + "HP:0100576" + ], + "urinary bladder inflammation": [ + "HP:0100577" + ], + "cystitis of the urinary bladder": [ + "HP:0100577" + ], + "lipoatrophy": [ + "HP:0100578" + ], + "atrophy of fat": [ + "HP:0100578" + ], + "loss of fat tissue in localised area": [ + "HP:0100578" + ], + "loss of fat tissue in localized area": [ + "HP:0100578" + ], + "mucosal telangiectasiae": [ + "HP:0100579" + ], + "barrett esophagus": [ + "HP:0100580" + ], + "barret syndrome": [ + "HP:0100580" + ], + "barrett oesophagus": [ + "HP:0100580" + ], + "barrett 's esophagus": [ + "HP:0100580" + ], + "barrett 's oesophagus": [ 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"HP:0100590" + ], + "peritoneal abscess": [ + "HP:0100592" + ], + "calcification of cartilage": [ + "HP:0100593" + ], + "esophageal web": [ + "HP:0100594" + ], + "camptocormia": [ + "HP:0100595" + ], + "absent naris": [ + "HP:0100596" + ], + "absent nares": [ + "HP:0100596" + ], + "abouphalia": [ + "HP:0100596" + ], + "aplasia of the naris": [ + "HP:0100596" + ], + "aplasia of the nares": [ + "HP:0100596" + ], + "aplasia / hypoplasia of the naris": [ + "HP:0100596" + ], + "aplasia / hypoplasia of the nares": [ + "HP:0100596" + ], + "miss nostril": [ + "HP:0100596" + ], + "missing nostrils": [ + "HP:0100596" + ], + "pulmonary edema": [ + "HP:0100598" + ], + "excess fluid in lung": [ + "HP:0100598" + ], + "excess fluid in lungs": [ + "HP:0100598" + ], + "lung edema": [ + "HP:0100598" + ], + "lung oedema": [ + "HP:0100598" + ], + "pulmonary oedema": [ + "HP:0100598" + ], + "wet lung": [ + "HP:0100598" + ], + "bifid penis": [ + "HP:0100599" + ], + "diphallia": [ + "HP:0100599" + ], + "penile duplication": [ + "HP:0100599" + ], + "penoscrotal transposition": [ + "HP:0100600" + ], + "prepenile scrotum": [ + "HP:0100600" + ], + "eclampsia": [ + "HP:0100601" + ], + "preeclampsia": [ + "HP:0100602" + ], + "pre - eclampsia": [ + "HP:0100602" + ], + "toxemia of pregnancy": [ + "HP:0100603" + ], + "hypertensive disorder of pregnancy": [ + "HP:0100603" + ], + "toxaemia of pregnancy": [ + "HP:0100603" + ], + "neoplasm of the lip": [ + "HP:0100604" + ], + "lip tumor": [ + "HP:0100604" + ], + "lip tumour": [ + "HP:0100604" + ], + "neoplasia of the lip": [ + "HP:0100604" + ], + "tumor of the lip": [ + "HP:0100604" + ], + "tumour of the lip": [ + "HP:0100604" + ], + "neoplasm of the larynx": [ + "HP:0100605" + ], + "neoplasm of the respiratory system": [ + "HP:0100606" + ], + "respiratory system tumor": [ + "HP:0100606" + ], + "respiratory system tumour": [ + "HP:0100606" + ], + "dysmenorrhea": [ + "HP:0100607" + ], + "painful menstruation": [ + "HP:0100607" + ], + 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neoplasia": [ + "HP:0100615" + ], + "ovarian tumor": [ + "HP:0100615" + ], + "ovarian tumour": [ + "HP:0100615" + ], + "testicular teratoma": [ + "HP:0100616" + ], + "testicular seminoma": [ + "HP:0100617" + ], + "leydig cell neoplasia": [ + "HP:0100618" + ], + "sertoli cell neoplasm": [ + "HP:0100619" + ], + "sertoli cell neoplasia": [ + "HP:0100619" + ], + "germinoma": [ + "HP:0100620" + ], + "dysgerminoma": [ + "HP:0100621" + ], + "maternal seizure": [ + "HP:0100622" + ], + "maternal seizures": [ + "HP:0100622" + ], + "abnormality of corpus cavernosum": [ + "HP:0100623" + ], + "corpus cavernosum sclerosis": [ + "HP:0100624" + ], + "enlarge thorax": [ + "HP:0100625" + ], + "enlarged thorax": [ + "HP:0100625" + ], + "wide rib cage": [ + "HP:0100625" + ], + "wide thorax": [ + "HP:0100625" + ], + "chronic hepatic failure": [ + "HP:0100626" + ], + "chronic liver failure": [ + "HP:0100626" + ], + "displacement of the urethral meatus": [ + "HP:0100627" + ], + "displacement of the external 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oral mucosa": [ + "HP:0100669" + ], + "abnormal color of the oral mucosa": [ + "HP:0100669" + ], + "abnormal colour of the oral mucosa": [ + "HP:0100669" + ], + "abnormal pigmentation of oral cavity": [ + "HP:0100669" + ], + "abnormal pigmentation of oral mucous membrane": [ + "HP:0100669" + ], + "abnormal pigmentation of the oral mucosa / gingiva": [ + "HP:0100669" + ], + "abnormal pigmentation of the oral mucosa / gingivae": [ + "HP:0100669" + ], + "coarse metaphyseal trabecularization": [ + "HP:0100670" + ], + "coarse trabeculation at metaphyses": [ + "HP:0100670" + ], + "rough bone trabeculation": [ + "HP:0100670" + ], + "rough trabeculation of bone": [ + "HP:0100670" + ], + "abnormal trabecular bone morphology": [ + "HP:0100671" + ], + "abnormal shape of spongy bone": [ + "HP:0100671" + ], + "abnormality of bone trabeculation": [ + "HP:0100671" + ], + "vaginal hernia": [ + "HP:0100672" + ], + "vaginal hydrocele": [ + "HP:0100673" + ], + "vaginal hematocele": [ + "HP:0100674" + ], 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"abnormal thoracic spine morphology": [ + "HP:0100711" + ], + "abnormality of the thoracic spine": [ + "HP:0100711" + ], + "abnormal lumbar spine morphology": [ + "HP:0100712" + ], + "abnormality of the lumbar spine": [ + "HP:0100712" + ], + "self - injurious behavior": [ + "HP:0100716" + ], + "autoagression": [ + "HP:0100716" + ], + "self injury": [ + "HP:0100716" + ], + "self - harm": [ + "HP:0100716" + ], + "self - injurious behaviors": [ + "HP:0100716" + ], + "self - injurious behaviour": [ + "HP:0100716" + ], + "self - injurious behaviours": [ + "HP:0100716" + ], + "abnormal cementum morphology": [ + "HP:0100717" + ], + "abnormality of the cementum": [ + "HP:0100717" + ], + "uterine rupture": [ + "HP:0100718" + ], + "lens coloboma": [ + "HP:0100719" + ], + "hypoplasia of the ear cartilage": [ + "HP:0100720" + ], + "underdeveloped ear cartilage": [ + "HP:0100720" + ], + "mediastinal lymphadenopathy": [ + "HP:0100721" + ], + "swollen lymph node in center of chest": [ + "HP:0100721" 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face": [ + "HP:0100729" + ], + "large facies": [ + "HP:0100729" + ], + "bronchogenic cyst": [ + "HP:0100730" + ], + "transverse facial cleft": [ + "HP:0100731" + ], + "lateral facial cleft": [ + "HP:0100731" + ], + "pancreatic fibrosis": [ + "HP:0100732" + ], + "neoplasm of the parathyroid gland": [ + "HP:0100733" + ], + "parathyroid neoplasia": [ + "HP:0100733" + ], + "abnormality of vertebral epiphysis morphology": [ + "HP:0100734" + ], + "abnormal shape of the end part of the vertebra bone": [ + "HP:0100734" + ], + "abnormality of the vertebral epiphysis": [ + "HP:0100734" + ], + "abnormality of the vertebral epiphyses": [ + "HP:0100734" + ], + "hypertensive crisis": [ + "HP:0100735" + ], + "abnormal soft palate morphology": [ + "HP:0100736" + ], + "abnormality of the muscular palate": [ + "HP:0100736" + ], + "abnormality of the soft palate": [ + "HP:0100736" + ], + "abnormality of the velum": [ + "HP:0100736" + ], + "abnormality of the velum palatinum": [ + "HP:0100736" + ], + "abnormal hard palate morphology": [ + "HP:0100737" + ], + "abnormality of the hard palate": [ + "HP:0100737" + ], + "abnormality of the secondary palate": [ + "HP:0100737" + ], + "abnormal eat behavior": [ + "HP:0100738" + ], + "abnormal eating behavior": [ + "HP:0100738" + ], + "abnormal eat behaviour": [ + "HP:0100738" + ], + "abnormal eating behaviour": [ + "HP:0100738" + ], + "bulimia": [ + "HP:0100739" + ], + "binge and purge": [ + "HP:0100739" + ], + "vascular neoplasm": [ + "HP:0100742" + ], + "blood vessel tumor": [ + "HP:0100742" + ], + "blood vessel tumour": [ + "HP:0100742" + ], + "neoplasm of the rectum": [ + "HP:0100743" + ], + "rectal tumor": [ + "HP:0100743" + ], + "rectal tumour": [ + "HP:0100743" + ], + "abnormality of the humeroradial joint": [ + "HP:0100744" + ], + "abnormality of the humeroulnar joint": [ + "HP:0100745" + ], + "macrodactyly of finger": [ + "HP:0100746" + ], + "macrodactyly of hand": [ + "HP:0100746" + ], + "macrodactyly of hands": [ + "HP:0100746" 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"HP:0100757" + ], + "gangrene": [ + "HP:0100758" + ], + "death of body tissue due to lack of blood flow or infection": [ + "HP:0100758" + ], + "clubbing of finger": [ + "HP:0100759" + ], + "clubbing of fingers": [ + "HP:0100759" + ], + "clubbed finger": [ + "HP:0100759" + ], + "clubbed fingers": [ + "HP:0100759" + ], + "clubbing ( hand )": [ + "HP:0100759" + ], + "clubbing ( hands )": [ + "HP:0100759" + ], + "finger club": [ + "HP:0100759" + ], + "finger clubbing": [ + "HP:0100759" + ], + "clubbing of toe": [ + "HP:0100760" + ], + "clubbing of toes": [ + "HP:0100760" + ], + "clubbed toe": [ + "HP:0100760" + ], + "clubbed toes": [ + "HP:0100760" + ], + "visceral angiomatosis": [ + "HP:0100761" + ], + "hemobilia": [ + "HP:0100762" + ], + "haemobilia": [ + "HP:0100762" + ], + "abnormality of the lymphatic system": [ + "HP:0100763" + ], + "lymphatic disease": [ + "HP:0100763" + ], + "lymphangioma": [ + "HP:0100764" + ], + "abnormality of the tonsil": [ + "HP:0100765" + ], + "abnormality of the tonsils": [ + "HP:0100765" + ], + "abnormal lymphatic vessel morphology": [ + "HP:0100766" + ], + "abnormality of the lymphatic vessel": [ + "HP:0100766" + ], + "abnormality of the lymphatic vessels": [ + "HP:0100766" + ], + "abnormal placenta morphology": [ + "HP:0100767" + ], + "abnormality of the placenta": [ + "HP:0100767" + ], + "placental issue": [ + "HP:0100767" + ], + "choriocarcinoma": [ + "HP:0100768" + ], + "synovitis": [ + "HP:0100769" + ], + "hyperperistalsis": [ + "HP:0100770" + ], + "stomach churn": [ + "HP:0100770" + ], + "stomach churning": [ + "HP:0100770" + ], + "hypoperistalsis": [ + "HP:0100771" + ], + "intestinal hypoperistalsis": [ + "HP:0100771" + ], + "cartilage destruction": [ + "HP:0100773" + ], + "hyperostosis": [ + "HP:0100774" + ], + "bone hypertrophy": [ + "HP:0100774" + ], + "bone overgrowth": [ + "HP:0100774" + ], + "dural ectasia": [ + "HP:0100775" + ], + "recurrent pharyngitis": [ + "HP:0100776" + ], + "pharyngitis , recurrent": [ + "HP:0100776" + ], + "recurrent sore throat": [ + "HP:0100776" + ], + "exostosis": [ + "HP:0100777" + ], + "exostoses": [ + "HP:0100777" + ], + "formation of new noncancerous bone on top of exist bone": [ + "HP:0100777" + ], + "formation of new noncancerous bone on top of existing bone": [ + "HP:0100777" + ], + "cryoglobulinemia": [ + "HP:0100778" + ], + "cryoprecipitable immune complex": [ + "HP:0100778" + ], + "cryoprecipitable immune complexes": [ + "HP:0100778" + ], + "urogenital sinus anomaly": [ + "HP:0100779" + ], + "conjunctival hamartoma": [ + "HP:0100780" + ], + "abnormal sacroiliac joint morphology": [ + "HP:0100781" + ], + "abnormality of the sacroiliac joint": [ + "HP:0100781" + ], + "breast aplasia": [ + "HP:0100783" + ], + "absent breast": [ + "HP:0100783" + ], + "congenital absence of breast": [ + "HP:0100783" + ], + "mammary gland aplasia": [ + "HP:0100783" + ], + "peripheral arteriovenous fistula": [ + "HP:0100784" + ], + "insomnia": [ + "HP:0100785" + ], + "difficulty stay or fall asleep": [ + "HP:0100785" + ], + "difficulty staying or falling asleep": [ + "HP:0100785" + ], + "fragment sleep": [ + "HP:0100785" + ], + "fragmented sleep": [ + "HP:0100785" + ], + "hypersomnia": [ + "HP:0100786" + ], + "excessive sleepiness": [ + "HP:0100786" + ], + "prostate neoplasm": [ + "HP:0100787" + ], + "fuse lip": [ + "HP:0100788" + ], + "fused lips": [ + "HP:0100788" + ], + "adhesion of upper and low lip": [ + "HP:0100788" + ], + "adhesion of upper and lower lips": [ + "HP:0100788" + ], + "fusion of upper and low lip": [ + "HP:0100788" + ], + "fusion of upper and lower lips": [ + "HP:0100788" + ], + "torus palatinus": [ + "HP:0100789" + ], + "maxillary torus": [ + "HP:0100789" + ], + "palatal torus": [ + "HP:0100789" + ], + "palatal tori": [ + "HP:0100789" + ], + "palate exostosis": [ + "HP:0100789" + ], + "palate exostoses": [ + "HP:0100789" + ], + "prominent midpalatal ridge": [ + "HP:0100789" + ], + "hernia": [ + "HP:0100790" + ], + "hernias": [ + "HP:0100790" + ], + "acantholysis": [ + "HP:0100792" + ], + "nikolsky 's sign": [ + "HP:0100792" + ], + "abnormally straight spine": [ + "HP:0100795" + ], + "orchitis": [ + "HP:0100796" + ], + "inflammation of testicle": [ + "HP:0100796" + ], + "inflammation of testicles": [ + "HP:0100796" + ], + "toenail dysplasia": [ + "HP:0100797" + ], + "abnormal toenail development": [ + "HP:0100797" + ], + "dysplastic toenail": [ + "HP:0100797" + ], + "dysplastic toenails": [ + "HP:0100797" + ], + "fingernail dysplasia": [ + "HP:0100798" + ], + "abnormal fingernail development": [ + "HP:0100798" + ], + "dysplastic fingernail": [ + "HP:0100798" + ], + "dysplastic fingernails": [ + "HP:0100798" + ], + "neoplasm of the middle ear": [ + "HP:0100799" + ], + "middle ear tumor": [ + "HP:0100799" + ], + "middle ear tumour": [ + "HP:0100799" + ], + "neoplasia of the middle ear": [ + "HP:0100799" + ], + "aplasia / hypoplasia of the pancreas": [ + "HP:0100800" + ], + "absent / small pancreas": [ + "HP:0100800" + ], + "absent / underdevelop pancreas": [ + "HP:0100800" + ], + "absent / underdeveloped pancreas": [ + "HP:0100800" + ], + "pancreatic aplasia": [ + "HP:0100801" + ], + "absent pancreas": [ + "HP:0100801" + ], + "malposition of the stomach": [ + "HP:0100802" + ], + "abnormal stomach location": [ + "HP:0100802" + ], + "gastric ectopia": [ + "HP:0100802" + ], + "gastric malposition": [ + "HP:0100802" + ], + "abnormality of the periungual region": [ + "HP:0100803" + ], + "ungual fibroma": [ + "HP:0100804" + ], + "koenen tumor": [ + "HP:0100804" + ], + "koenen tumour": [ + "HP:0100804" + ], + "koenen 's tumor": [ + "HP:0100804" + ], + "koenen 's tumour": [ + "HP:0100804" + ], + "parungual fibroma": [ + "HP:0100804" + ], + "parungual fibromas": [ + "HP:0100804" + ], + "periungual fibroma": [ + "HP:0100804" + ], + "obsolete precocious menopause": [ + "HP:0100805" + ], + "sepsis": [ + "HP:0100806" + ], + "infection in blood stream": [ + "HP:0100806" + ], + "long finger": [ + "HP:0100807" + ], + "long fingers": [ + "HP:0100807" + ], + "gastric diverticulum": [ + "HP:0100808" + ], + "stomach diverticulum": [ + "HP:0100808" + ], + "scalp tenderness": [ + "HP:0100809" + ], + "allodynia of scalp": [ + "HP:0100809" + ], + "scalp hypersensitivity": [ + "HP:0100809" + ], + "scalp pain": [ + "HP:0100809" + ], + "point helix": [ + "HP:0100810" + ], + "pointed helix": [ + "HP:0100810" + ], + "elfin ear": [ + "HP:0100810" + ], + "point ear": [ + "HP:0100810" + ], + "pointed ear": [ + "HP:0100810" + ], + "spock ear": [ + "HP:0100810" + ], + "spock 's ear": [ + "HP:0100810" + ], + "vulcan ear": [ + "HP:0100810" + ], + "aplasia / hypoplasia of the colon": [ + "HP:0100811" + ], + "absent / small colon": [ + "HP:0100811" + ], + "absent / underdevelop colon": [ + "HP:0100811" + ], + "absent / underdeveloped colon": [ + "HP:0100811" + ], + "halitosis": [ + "HP:0100812" + ], + "bad breath": [ + "HP:0100812" + ], + "foetor ex ore": [ + "HP:0100812" + ], + "testicular torsion": [ + "HP:0100813" + ], + "spermatic cord torsion": [ + "HP:0100813" + ], + "blue nevus": [ + "HP:0100814" + ], + "congenital dermal melanocytosis": [ + "HP:0100814" + ], + "mongolian spot": [ + "HP:0100814" + ], + "lip hyperpigmentation": [ + "HP:0100816" + ], + "darkening of skin of the lip": [ + "HP:0100816" + ], + "darkening of skin of the lips": [ + "HP:0100816" + ], + "hyperpigmentation of lip vermillion": [ + "HP:0100816" + ], + "increase pigmentation on the lip": [ + "HP:0100816" + ], + "increased pigmentation on the lips": [ + "HP:0100816" + ], + "renovascular hypertension": [ + "HP:0100817" + ], + "hypertension due to renal artery hyperplasia": [ + "HP:0100817" + ], + "long thorax": [ + "HP:0100818" + ], + "long rib cage": [ + "HP:0100818" + ], + "intestinal fistula": [ + "HP:0100819" + ], + "glomerulopathy": [ + "HP:0100820" + ], + "diseased glomerulus": [ + "HP:0100820" + ], + "diseased glomeruli": [ + "HP:0100820" + ], + "urethrocele": [ + "HP:0100821" + ], + "rectocele": [ + "HP:0100822" + ], + "genital hernia": [ + "HP:0100823" + ], + "cheilitis": [ + "HP:0100825" + ], + "inflammation of the lip": [ + "HP:0100825" + ], + "inflammation of the lips": [ + "HP:0100825" + ], + "red and sore lip": [ + "HP:0100825" + ], + "red and sore lips": [ + "HP:0100825" + ], + "neoplasm of the nail": [ + "HP:0100826" + ], + "nail tumor": [ + "HP:0100826" + ], + "nail tumour": [ + "HP:0100826" + ], + "lymphocytosis": [ + "HP:0100827" + ], + "high lymphocyte count": [ + "HP:0100827" + ], + "increase t cell count": [ + "HP:0100828" + ], + "increased t cell count": [ + "HP:0100828" + ], + "increase in t cell count": [ + "HP:0100828" + ], + "increase in t cell number": [ + "HP:0100828" + ], + "galactorrhea": [ + "HP:0100829" + ], + "galactorrhoea": [ + "HP:0100829" + ], + "spontaneous milk flow from breast": [ + "HP:0100829" + ], + "round ear": [ + "HP:0100830" + ], + "abnormality of vitamin k metabolism": [ + "HP:0100831" + ], + "vitreous floater": [ + "HP:0100832" + ], + "vitreous floaters": [ + "HP:0100832" + ], + "eye floater": [ + "HP:0100832" + ], + "eye floaters": [ + "HP:0100832" + ], + "flit fly": [ + "HP:0100832" + ], + "flitting flies": [ + "HP:0100832" + ], + "mouches volantes": [ + "HP:0100832" + ], + "myodeopsia": [ + "HP:0100832" + ], + "myodesopsia": [ + "HP:0100832" + ], + "spot in front of eye": [ + "HP:0100832" + ], + "spots in front of eyes": [ + "HP:0100832" + ], + "vitreous condensation": [ + "HP:0100832" + ], + "vitreous condensations": [ + "HP:0100832" + ], + "vitreous debris": [ + "HP:0100832" + ], + "vitreous opacity": [ + "HP:0100832" + ], + "vitreous opacities": [ + "HP:0100832" + ], + "vitreous veil": [ + "HP:0100832" + ], + "vitreous veils": [ + "HP:0100832" + ], + "neoplasm of the small intestine": [ + "HP:0100833" + ], + "small intestine tumor": [ + "HP:0100833" + ], + "small intestine tumour": [ + "HP:0100833" + ], + "neoplasm of the large intestine": [ + "HP:0100834" + ], + "large intestine tumor": [ + "HP:0100834" + ], + "large intestine tumour": [ + "HP:0100834" + ], + "benign neoplasm of the central nervous system": [ + "HP:0100835" + ], + "benign neoplasm of the cns": [ + "HP:0100835" + ], + "malignant neoplasm of the central nervous system": [ + "HP:0100836" + ], + "malignant neoplasm of the cns": [ + "HP:0100836" + ], + "atrophodermia vermiculata": [ + "HP:0100837" + ], + "vermiculata atrophoderma": [ + "HP:0100837" + ], + "recurrent cutaneous abscess formation": [ + "HP:0100838" + ], + "hepatic agenesis": [ + "HP:0100839" + ], + "fail liver development": [ + "HP:0100839" + ], + "failed liver development": [ + "HP:0100839" + ], + "liver agenesis": [ + "HP:0100839" + ], + "aplasia / hypoplasia of the eyebrow": [ + "HP:0100840" + ], + "absence of eyebrow": [ + "HP:0100840" + ], + "hypotrophic eyebrow": [ + "HP:0100840" + ], + "lack of eyebrow": [ + "HP:0100840" + ], + "missing eyebrow": [ + "HP:0100840" + ], + "sparse or absent eyebrow": [ + "HP:0100840" + ], + "sparse or absent eyebrows": [ + "HP:0100840" + ], + "sparse to absent eyebrow": [ + "HP:0100840" + ], + "sparse to absent eyebrows": [ + "HP:0100840" + ], + "sparse / absent eyebrow": [ + "HP:0100840" + ], + "sparse / absent eyebrows": [ + "HP:0100840" + ], + "microgastria": [ + "HP:0100841" + ], + "septo - optic dysplasia": [ + "HP:0100842" + ], + "de morsier syndrome": [ + "HP:0100842" + ], + "obsolete glioblastoma": [ + "HP:0100843" + ], + "pancreatic fistula": [ + "HP:0100844" + ], + "anaphylactic shock": [ + "HP:0100845" + ], + "anaphylaxis": [ + "HP:0100845" + ], + "palmoplantar pustulosis": [ + "HP:0100847" + ], + "palmoplantar pustule": [ + "HP:0100847" + ], + "palmoplantar pustules": [ + "HP:0100847" + ], + "pustulosis of palm and sol": [ + "HP:0100847" + ], + "pustulosis of palms and soles": [ + "HP:0100847" + ], + "pustulosis palmaris et plantaris": [ + "HP:0100847" + ], + "neoplasm of the male external genitalia": [ + "HP:0100848" + ], + "neoplasia of the male external genitalia": [ + "HP:0100848" + ], + "neoplasm of the scrotum": [ + "HP:0100849" + ], + "neoplasia of the scrotum": [ + "HP:0100849" + ], + "scrotum tumor": [ + "HP:0100849" + ], + "scrotum tumour": [ + "HP:0100849" + ], + "neoplasm of the penis": [ + "HP:0100850" + ], + "neoplasia of the penis": [ + "HP:0100850" + ], + "penis tumor": [ + "HP:0100850" + ], + "penis tumour": [ + "HP:0100850" + ], + "abnormal emotion / affect behavior": [ + "HP:0100851" + ], + "abnormal emotion / affect behaviour": [ + "HP:0100851" + ], + "abnormal fear / anxiety - related behavior": [ + "HP:0100852" + ], + "abnormal fear / anxiety - relate behaviour": [ + "HP:0100852" + ], + "abnormal fear / anxiety - related behaviour": [ + "HP:0100852" + ], + "hypoplastic areola": [ + "HP:0100853" + ], + "hypoplastic areolae": [ + "HP:0100853" + ], + "aplasia of the musculature": [ + "HP:0100854" + ], + "absent musculature": [ + "HP:0100854" + ], + "triceps hypoplasia": [ + "HP:0100855" + ], + "small triceps": [ + "HP:0100855" + ], + "underdeveloped triceps": [ + "HP:0100855" + ], + "poorly ossify vertebra": [ + "HP:0100856" + ], + "poorly ossified vertebrae": [ + "HP:0100856" + ], + "flat sella turcica": [ + "HP:0100857" + ], + "dilatation of celiac artery": [ + "HP:0100858" + ], + "celiac artery aneurysm": [ + "HP:0100858" + ], + "coeliac artery aneurysm": [ + "HP:0100858" + ], + "dilatation of coeliac artery": [ + "HP:0100858" + ], + "dilatation of superior mesenteric artery": [ + "HP:0100859" + ], + "superior mesenteric artery aneurysm": [ + "HP:0100859" + ], + "dilatation of inferior mesenteric artery": [ + "HP:0100860" + ], + "inferior mesenteric artery aneurysm": [ + "HP:0100860" + ], + "sclerotic vertebral body": [ + "HP:0100861" + ], + "vertebral body sclerosis": [ + "HP:0100861" + ], + "aplasia of the femoral head": [ + "HP:0100862" + ], + "absent femoral head": [ + "HP:0100862" + ], + "aplasia of the femoral neck": [ + "HP:0100863" + ], + "absent neck of thighbone": [ + "HP:0100863" + ], + "short femoral neck": [ + "HP:0100864" + ], + "hypoplasia of the femoral neck": [ + "HP:0100864" + ], + "hypoplastic femoral neck": [ + "HP:0100864" + ], + "short femoral necks": [ + "HP:0100864" + ], + "short neck of thighbone": [ + "HP:0100864" + ], + "broad ischia": [ + "HP:0100865" + ], + "short iliac bone": [ + "HP:0100866" + ], + "short iliac bones": [ + "HP:0100866" + ], + "short pelvis bone": [ + "HP:0100866" + ], + "short pelvis bones": [ + "HP:0100866" + ], + "duodenal stenosis": [ + "HP:0100867" + ], + "duodenal stenosis / atresia": [ + "HP:0100867" + ], + "palmar telangiectasia": [ + "HP:0100869" + ], + "telangiectases of palm and sol": [ + "HP:0100869" + ], + "telangiectases of palms and soles": [ + "HP:0100869" + ], + "teleangiectases of palm": [ + "HP:0100869" + ], + "teleangiectases of palms": [ + "HP:0100869" + ], + "plantar telangiectasia": [ + "HP:0100870" + ], + "plantar teleangiectasia": [ + "HP:0100870" + ], + "telangiectases of sol": [ + "HP:0100870" + ], + "telangiectases of soles": [ + "HP:0100870" + ], + "teleangiectases of sol": [ + "HP:0100870" + ], + "teleangiectases of soles": [ + "HP:0100870" + ], + "abnormality of the palm": [ + "HP:0100871" + ], + "abnormality of the plantar skin of foot": [ + "HP:0100872" + ], + "minor foot anomaly": [ + "HP:0100872" + ], + "minor feet anomalies": [ + "HP:0100872" + ], + "thick hair": [ + "HP:0100874" + ], + "increase follicular density": [ + "HP:0100874" + ], + "increased follicular density": [ + "HP:0100874" + ], + "increase hair density": [ + "HP:0100874" + ], + "increased hair density": [ + "HP:0100874" + ], + "hemimacroglossia": [ + "HP:0100875" + ], + "hemiglossal hyperplasia": [ + "HP:0100875" + ], + "hemiglossal hypertrophy": [ + "HP:0100875" + ], + "hyperplasia of half of the tongue": [ + "HP:0100875" + ], + "hypertrophy of half of the tongue": [ + "HP:0100875" + ], + "increase size of half of the tongue": [ + "HP:0100875" + ], + "increased size of half of the tongue": [ + "HP:0100875" + ], + "large half of tongue": [ + "HP:0100875" + ], + "infra - orbital crease": [ + "HP:0100876" + ], + "crease in skin under the eye": [ + "HP:0100876" + ], + "groove in skin under the eye": [ + "HP:0100876" + ], + "infraorbital crease": [ + "HP:0100876" + ], + "infraorbital creases": [ + "HP:0100876" + ], + "underorbital skin crease": [ + "HP:0100876" + ], + "underorbital skin creases": [ + "HP:0100876" + ], + "renal diverticulum": [ + "HP:0100877" + ], + "caliceal diverticulum": [ + "HP:0100877" + ], + "pelvic diverticulum": [ + "HP:0100877" + ], + "renal pelvic diverticulum": [ + "HP:0100877" + ], + "enlarge uterus": [ + "HP:0100878" + ], + "enlarged uterus": [ + "HP:0100878" + ], + "enlarge ovary": [ + "HP:0100879" + ], + "enlarged ovaries": [ + "HP:0100879" + ], + "nephrogenic rest": [ + "HP:0100880" + ], + "congenital mesoblastic nephroma": [ + "HP:0100881" + ], + "fibrous hamartoma": [ + "HP:0100882" + ], + "fibrous hamartoma of infancy": [ + "HP:0100882" + ], + "chorangioma": [ + "HP:0100883" + ], + "placental hamartoma": [ + "HP:0100883" + ], + "compensatory scoliosis": [ + "HP:0100884" + ], + "lateral venous anomaly": [ + "HP:0100885" + ], + "lateral marginal vein of servelle": [ + "HP:0100885" + ], + "vein of servelle": [ + "HP:0100885" + ], + "abnormality of globe location": [ + "HP:0100886" + ], + "abnormality of eyeball location": [ + "HP:0100886" + ], + "abnormality of eyeball position": [ + "HP:0100886" + ], + "abnormality of globe position": [ + "HP:0100886" + ], + "abnormality of globe size": [ + "HP:0100887" + ], + "abnormality of eyeball size": [ + "HP:0100887" + ], + "eye size difference": [ + "HP:0100887" + ], + "interdigital loop": [ + "HP:0100888" + ], + "interdigital loops": [ + "HP:0100888" + ], + "abnormality of the ductus choledochus": [ + "HP:0100889" + ], + "abnormality of the common bile duct": [ + "HP:0100889" + ], + "cyst of the ductus choledochus": [ + "HP:0100890" + ], + "choledochal cyst": [ + "HP:0100890" + ], + "bifid xiphoid process": [ + "HP:0100891" + ], + "bifid xiphisternum": [ + "HP:0100891" + ], + "abnormality of the xiphoid process": [ + "HP:0100892" + ], + "prominent xiphoid process": [ + "HP:0100893" + ], + "prominent xiphisternum": [ + "HP:0100893" + ], + "broad xiphoid process": [ + "HP:0100894" + ], + "broad xiphisternum": [ + "HP:0100894" + ], + "rectal polyposis": [ + "HP:0100896" + ], + "multiple rectal polyp": [ + "HP:0100896" + ], + "multiple rectal polyps": [ + "HP:0100896" + ], + "rectal polyp": [ + "HP:0100896" + ], + "rectal polyps": [ + "HP:0100896" + ], + "connective tissue nevus": [ + "HP:0100898" + ], + "connective tissue nevi": [ + "HP:0100898" + ], + "sclerosis of finger phalanx": [ + "HP:0100899" + ], + "increase bone density in the finger bone": [ + "HP:0100899" + ], + "increased bone density in the finger bone": [ + "HP:0100899" + ], + "sclerosis of the phalanx of the hand": [ + "HP:0100899" + ], + "sclerosis of the phalanges of the hand": [ + "HP:0100899" + ], + "sclerosis of the distal phalanx of the 2nd finger": [ + "HP:0100900" + ], + "increase bone density in the outermost bone of the index finger": [ + "HP:0100900" + ], + "increased bone density in the outermost bone of the index finger": [ + "HP:0100900" + ], + "sclerosis of the distal phalanx of the 3rd finger": [ + "HP:0100901" + ], + "increase bone density in the outermost bone of the middle finger": [ + "HP:0100901" + ], + "increased bone density in the outermost bone of the middle finger": [ + "HP:0100901" + ], + "sclerosis of the distal phalanx of the 4th finger": [ + "HP:0100902" + ], + "increase bone density in the outermost bone of the ring finger": [ + "HP:0100902" + ], + "increased bone density in the outermost bone of the ring finger": [ + "HP:0100902" + ], + "sclerosis of the distal phalanx of the 5th finger": [ + "HP:0100903" + ], + "increase bone density in the outermost little finger bone": [ + "HP:0100903" + ], + "increased bone density in the outermost little finger bone": [ + "HP:0100903" + ], + "increase bone density in the outermost pinkie finger bone": [ + "HP:0100903" + ], + "increased bone density in the outermost pinkie finger bone": [ + "HP:0100903" + ], + "increase bone density in the outermost pinky finger bone": [ + "HP:0100903" + ], + "increased bone density in the outermost pinky finger bone": [ + "HP:0100903" + ], + "sclerosis of the middle phalanx of the 2nd finger": [ + "HP:0100904" + ], + "increase bone density in the middle bone of the index finger": [ + "HP:0100904" + ], + "increased bone density in the middle bone of the index finger": [ + "HP:0100904" + ], + "sclerosis of the middle phalanx of the 3rd finger": [ + "HP:0100905" + ], + "increase bone density in the middle bone of the middle finger": [ + "HP:0100905" + ], + "increased bone density in the middle bone of the middle finger": [ + "HP:0100905" + ], + "sclerosis of the middle phalanx of the 4th finger": [ + "HP:0100906" + ], + "increase bone density in the middle bone of the ring finger": [ + "HP:0100906" + ], + "increased bone density in the middle bone of the ring finger": [ + "HP:0100906" + ], + "sclerosis of the middle phalanx of the 5th finger": [ + "HP:0100907" + ], + "increase bone density in the middle bone of the little finger": [ + "HP:0100907" + ], + "increased bone density in the middle bone of the little finger": [ + "HP:0100907" + ], + "increase bone density in the middle bone of the pinkie finger": [ + "HP:0100907" + ], + "increased bone density in the middle bone of the pinkie finger": [ + "HP:0100907" + ], + "increase bone density in the middle bone of the pinky finger": [ + "HP:0100907" + ], + "increased bone density in the middle bone of the pinky finger": [ + "HP:0100907" + ], + "sclerosis of the proximal phalanx of the 2nd finger": [ + "HP:0100908" + ], + "increase bone density in the innermost bone of the index finger": [ + "HP:0100908" + ], + "increased bone density in the innermost bone of the index finger": [ + "HP:0100908" + ], + "sclerosis of the proximal phalanx of the 3rd finger": [ + "HP:0100909" + ], + "increase bone density in innermost bone of the middle finger": [ + "HP:0100909" + ], + "increased bone density in innermost bone of the middle finger": [ + "HP:0100909" + ], + "sclerosis of the proximal phalanx of the 4th finger": [ + "HP:0100910" + ], + "increase bone density in the innermost bone of the ring finger": [ + "HP:0100910" + ], + "increased bone density in the innermost bone of the ring finger": [ + "HP:0100910" + ], + "sclerosis of the proximal phalanx of the 5th finger": [ + "HP:0100911" + ], + "increase bone density in innermost little finger bone": [ + "HP:0100911" + ], + "increased bone density in innermost little finger bone": [ + "HP:0100911" + ], + "increase bone density in innermost pinkie finger bone": [ + "HP:0100911" + ], + "increased bone density in innermost pinkie finger bone": [ + "HP:0100911" + ], + "increase bone density in innermost pinky finger bone": [ + "HP:0100911" + ], + "increased bone density in innermost pinky finger bone": [ + "HP:0100911" + ], + "sclerosis of the distal phalanx of the thumb": [ + "HP:0100912" + ], + "increase bone density in the outermost bone of the thumb": [ + "HP:0100912" + ], + "increased bone density in the outermost bone of the thumb": [ + "HP:0100912" + ], + "sclerosis of the proximal phalanx of the thumb": [ + "HP:0100913" + ], + "increase bone density in the innermost bone of the thumb": [ + "HP:0100913" + ], + "increased bone density in the innermost bone of the thumb": [ + "HP:0100913" + ], + "sclerosis of the 1st metacarpal": [ + "HP:0100914" + ], + "increase bone density in 1st long bone of hand": [ + "HP:0100914" + ], + "increased bone density in 1st long bone of hand": [ + "HP:0100914" + ], + "sclerosis of distal finger phalanx": [ + "HP:0100915" + ], + "increase bone density in outermost finger bone": [ + "HP:0100915" + ], + "increased bone density in outermost finger bone": [ + "HP:0100915" + ], + "sclerosis of the distal phalanx of the hand": [ + "HP:0100915" + ], + "sclerosis of the distal phalanges of the hand": [ + "HP:0100915" + ], + "sclerosis of middle finger phalanx": [ + "HP:0100916" + ], + "increase bone density in middle finger bone of hand": [ + "HP:0100916" + ], + "increased bone density in middle finger bone of hand": [ + "HP:0100916" + ], + "sclerosis of the middle phalanx of the hand": [ + "HP:0100916" + ], + "sclerosis of the middle phalanges of the hand": [ + "HP:0100916" + ], + "sclerosis of proximal finger phalanx": [ + "HP:0100917" + ], + "increase bone density in innermost finger bone": [ + "HP:0100917" + ], + "increased bone density in innermost finger bone": [ + "HP:0100917" + ], + "sclerosis of the proximal phalanx of the hand": [ + "HP:0100917" + ], + "sclerosis of the proximal phalanges of the hand": [ + "HP:0100917" + ], + "sclerosis of 2nd finger phalanx": [ + "HP:0100918" + ], + "increase bone density in 2nd finger bone": [ + "HP:0100918" + ], + "increased bone density in 2nd finger bone": [ + "HP:0100918" + ], + "sclerosis of the phalanx of the 2nd finger": [ + "HP:0100918" + ], + "sclerosis of the phalanges of the 2nd finger": [ + "HP:0100918" + ], + "sclerosis of 3rd finger phalanx": [ + "HP:0100919" + ], + "increase bone density in middle finger bone": [ + "HP:0100919" + ], + "increased bone density in middle finger bone": [ + "HP:0100919" + ], + "sclerosis of the phalanx of the 3rd finger": [ + "HP:0100919" + ], + "sclerosis of the phalanges of the 3rd finger": [ + "HP:0100919" + ], + "sclerosis of 4th finger phalanx": [ + "HP:0100920" + ], + "increase bone density in ring finger bone": [ + "HP:0100920" + ], + "increased bone density in ring finger bone": [ + "HP:0100920" + ], + "sclerosis of the phalanx of the 4th finger": [ + "HP:0100920" + ], + "sclerosis of the phalanges of the 4th finger": [ + "HP:0100920" + ], + "sclerosis of 5th finger phalanx": [ + "HP:0100921" + ], + "increase bone density in little finger bone": [ + "HP:0100921" + ], + "increased bone density in little finger bone": [ + "HP:0100921" + ], + "increase bone density in pinkie finger bone": [ + "HP:0100921" + ], + "increased bone density in pinkie finger bone": [ + "HP:0100921" + ], + "increase bone density in pinky finger bone": [ + "HP:0100921" + ], + "increased bone density in pinky finger bone": [ + "HP:0100921" + ], + "sclerosis of the phalanx of the 5th finger": [ + "HP:0100921" + ], + "sclerosis of the phalanges of the 5th finger": [ + "HP:0100921" + ], + "sclerosis of thumb phalanx": [ + "HP:0100922" + ], + "increase bone density in thumb bone": [ + "HP:0100922" + ], + "increased bone density in thumb bone": [ + "HP:0100922" + ], + "sclerosis of the phalanx of the thumb": [ + "HP:0100922" + ], + "sclerosis of the phalanges of the thumb": [ + "HP:0100922" + ], + "clavicular sclerosis": [ + "HP:0100923" + ], + "increase bone density in collarbone": [ + "HP:0100923" + ], + "increased bone density in collarbone": [ + "HP:0100923" + ], + "osteosclerosis of the clavicle": [ + "HP:0100923" + ], + "osteosclerosis of the clavicles": [ + "HP:0100923" + ], + "sclerosis of toe phalanx": [ + "HP:0100924" + ], + "increase bone density in the toe bone": [ + "HP:0100924" + ], + "increased bone density in the toe bone": [ + "HP:0100924" + ], + "sclerosis of the phalanx of the toe": [ + "HP:0100924" + ], + "sclerosis of the phalanges of the toes": [ + "HP:0100924" + ], + "sclerosis of foot bone": [ + "HP:0100925" + ], + "increase bone density in foot bone": [ + "HP:0100925" + ], + "increased bone density in foot bone": [ + "HP:0100925" + ], + "sclerosis of bone of the foot": [ + "HP:0100925" + ], + "sclerosis of bones of the feet": [ + "HP:0100925" + ], + "sclerosis of 2nd toe phalanx": [ + "HP:0100926" + ], + "increase bone density in 2nd toe bone": [ + "HP:0100926" + ], + "increased bone density in 2nd toe bone": [ + "HP:0100926" + ], + "sclerosis of the phalanx of the 2nd toe": [ + "HP:0100926" + ], + "sclerosis of the phalanges of the 2nd toe": [ + "HP:0100926" + ], + "sclerosis of 3rd toe phalanx": [ + "HP:0100927" + ], + "increase bone density in 3rd toe bone": [ + "HP:0100927" + ], + "increased bone density in 3rd toe bone": [ + "HP:0100927" + ], + "sclerosis of the phalanx of the 3rd toe": [ + "HP:0100927" + ], + "sclerosis of the phalanges of the 3rd toe": [ + "HP:0100927" + ], + "sclerosis of 4th toe phalanx": [ + "HP:0100928" + ], + "increase bone density in 4th toe bone": [ + "HP:0100928" + ], + "increased bone density in 4th toe bone": [ + "HP:0100928" + ], + "sclerosis of the phalanx of the 4th toe": [ + "HP:0100928" + ], + "sclerosis of the phalanges of the 4th toe": [ + "HP:0100928" + ], + "sclerosis of 5th toe phalanx": [ + "HP:0100929" + ], + "increase bone density in little toe bone": [ + "HP:0100929" + ], + "increased bone density in little toe bone": [ + "HP:0100929" + ], + "increase bone density in pinkie toe bone": [ + "HP:0100929" + ], + "increased bone density in pinkie toe bone": [ + "HP:0100929" + ], + "increase bone density in pinky toe bone": [ + "HP:0100929" + ], + "increased bone density in pinky toe bone": [ + "HP:0100929" + ], + "sclerosis of the phalanx of the 5th toe": [ + "HP:0100929" + ], + "sclerosis of the phalanges of the 5th toe": [ + "HP:0100929" + ], + "sclerosis of hallux phalanx": [ + "HP:0100930" + ], + "increase bone density in big toe bone": [ + "HP:0100930" + ], + "increased bone density in big toe bone": [ + "HP:0100930" + ], + "sclerosis of the phalanx of the hallux": [ + "HP:0100930" + ], + "sclerosis of the phalanges of the hallux": [ + "HP:0100930" + ], + "sclerosis of the proximal phalanx of the 2nd toe": [ + "HP:0100931" + ], + "increase bone density in the innermost bone of the 2nd toe": [ + "HP:0100931" + ], + "increased bone density in the innermost bone of the 2nd toe": [ + "HP:0100931" + ], + "sclerosis of the proximal phalanx of the 3rd toe": [ + "HP:0100932" + ], + "increase bone density in the innermost bone of the 3rd toe": [ + "HP:0100932" + ], + "increased bone density in the innermost bone of the 3rd toe": [ + "HP:0100932" + ], + "sclerosis of the proximal phalanx of the 4th toe": [ + "HP:0100933" + ], + "increase bone density in the innermost bone of the 4th toe": [ + "HP:0100933" + ], + "increased bone density in the innermost bone of the 4th toe": [ + "HP:0100933" + ], + "sclerosis of the proximal phalanx of the 5th toe": [ + "HP:0100934" + ], + "increase bone density in the innermost bone of the little toe": [ + "HP:0100934" + ], + "increased bone density in the innermost bone of the little toe": [ + "HP:0100934" + ], + "increase bone density in the innermost bone of the pinkie toe": [ + "HP:0100934" + ], + "increased bone density in the innermost bone of the pinkie toe": [ + "HP:0100934" + ], + "increase bone density in the innermost bone of the pinky toe": [ + "HP:0100934" + ], + "increased bone density in the innermost bone of the pinky toe": [ + "HP:0100934" + ], + "sclerosis of the middle phalanx of the 2nd toe": [ + "HP:0100935" + ], + "increase bone density in the middle bone of the 2nd toe": [ + "HP:0100935" + ], + "increased bone density in the middle bone of the 2nd toe": [ + "HP:0100935" + ], + "sclerosis of the middle phalanx of the 3rd toe": [ + "HP:0100936" + ], + "increase bone density in the middle bone of the 3rd toe": [ + "HP:0100936" + ], + "increased bone density in the middle bone of the 3rd toe": [ + "HP:0100936" + ], + "sclerosis of the middle phalanx of the 4th toe": [ + "HP:0100937" + ], + "increase bone density in the middle bone of the 4th toe": [ + "HP:0100937" + ], + "increased bone density in the middle bone of the 4th toe": [ + "HP:0100937" + ], + "sclerosis of the middle phalanx of the 5th toe": [ + "HP:0100938" + ], + "increase bone density in the middle bone of the little toe": [ + "HP:0100938" + ], + "increased bone density in the middle bone of the little toe": [ + "HP:0100938" + ], + "increase bone density in the middle bone of the pinkie toe": [ + "HP:0100938" + ], + "increased bone density in the middle bone of the pinkie toe": [ + "HP:0100938" + ], + "increase bone density in the middle bone of the pinky toe": [ + "HP:0100938" + ], + "increased bone density in the middle bone of the pinky toe": [ + "HP:0100938" + ], + "sclerosis of the distal phalanx of the 2nd toe": [ + "HP:0100939" + ], + "increase bone density in the outermost bone of the 2nd toe": [ + "HP:0100939" + ], + "increased bone density in the outermost bone of the 2nd toe": [ + "HP:0100939" + ], + "sclerosis of the distal phalanx of the 3rd toe": [ + "HP:0100940" + ], + "increase bone density in the outermost bone of the 3rd toe": [ + "HP:0100940" + ], + "increased bone density in the outermost bone of the 3rd toe": [ + "HP:0100940" + ], + "sclerosis of the distal phalanx of the 4th toe": [ + "HP:0100941" + ], + "increase bone density in the outermost bone of the 4th toe": [ + "HP:0100941" + ], + "increased bone density in the outermost bone of the 4th toe": [ + "HP:0100941" + ], + "sclerosis of the distal phalanx of the 5th toe": [ + "HP:0100942" + ], + "increase bone density in the outermost bone of the little toe": [ + "HP:0100942" + ], + "increased bone density in the outermost bone of the little toe": [ + "HP:0100942" + ], + "increase bone density in the outermost bone of the pinkie toe": [ + "HP:0100942" + ], + "increased bone density in the outermost bone of the pinkie toe": [ + "HP:0100942" + ], + "increase bone density in the outermost bone of the pinky toe": [ + "HP:0100942" + ], + "increased bone density in the outermost bone of the pinky toe": [ + "HP:0100942" + ], + "sclerosis of the proximal phalanx of the hallux": [ + "HP:0100943" + ], + "increase bone density in the innermost bone of the big toe": [ + "HP:0100943" + ], + "increased bone density in the innermost bone of the big toe": [ + "HP:0100943" + ], + "sclerosis of the distal phalanx of the hallux": [ + "HP:0100944" + ], + "increase bone density in the outermost bone of the big toe": [ + "HP:0100944" + ], + "increased bone density in the outermost bone of the big toe": [ + "HP:0100944" + ], + "sclerosis of the 1st metatarsal": [ + "HP:0100945" + ], + "increase bone density in the 1st long bone of foot": [ + "HP:0100945" + ], + "increased bone density in the 1st long bone of foot": [ + "HP:0100945" + ], + "sclerosis of proximal toe phalanx": [ + "HP:0100946" + ], + "increase bone density in innermost toe bone": [ + "HP:0100946" + ], + "increased bone density in innermost toe bone": [ + "HP:0100946" + ], + "sclerosis of the proximal phalanx of the toe": [ + "HP:0100946" + ], + "sclerosis of the proximal phalanges of the toes": [ + "HP:0100946" + ], + "sclerosis of middle toe phalanx": [ + "HP:0100947" + ], + "increase bone density in middle toe bone": [ + "HP:0100947" + ], + "increased bone density in middle toe bone": [ + "HP:0100947" + ], + "sclerosis of the middle phalanx of the toe": [ + "HP:0100947" + ], + "sclerosis of the middle phalanges of the toes": [ + "HP:0100947" + ], + "sclerosis of distal toe phalanx": [ + "HP:0100948" + ], + "increase bone density in the outermost bone of the toe": [ + "HP:0100948" + ], + "increased bone density in the outermost bone of the toes": [ + "HP:0100948" + ], + "sclerosis of the distal phalanx of the toe": [ + "HP:0100948" + ], + "sclerosis of the distal phalanges of the toes": [ + "HP:0100948" + ], + "decrease 3 - hydroxyacyl - coa dehydrogenase level": [ + "HP:0100950" + ], + "decreased 3 - hydroxyacyl - coa dehydrogenase level": [ + "HP:0100950" + ], + "long chain 3 hydroxyacyl coa dehydrogenase deficiency": [ + "HP:0100950" + ], + "medium and short - chain l - 3 - hydroxyacyl - coenzyme a dehydrogenase deficiency": [ + "HP:0100950" + ], + "short - chain 3 - hydroxyacyl - coenzyme a dehydrogenase deficiency": [ + "HP:0100950" + ], + "enlarge fossa interpeduncularis": [ + "HP:0100951" + ], + "enlarged fossa interpeduncularis": [ + "HP:0100951" + ], + "enlarge basal cistern": [ + "HP:0100951" + ], + "enlarged basal cistern": [ + "HP:0100951" + ], + "enlarge interpeduncular cistern": [ + "HP:0100951" + ], + "enlarged interpeduncular cistern": [ + "HP:0100951" + ], + "enlarge sylvian cistern": [ + "HP:0100952" + ], + "enlarged sylvian cistern": [ + "HP:0100952" + ], + "enlarged lateral fissure": [ + "HP:0100952" + ], + "enlarged lateral sulcus": [ + "HP:0100952" + ], + "enlarge sylvian fissure": [ + "HP:0100952" + ], + "enlarged sylvian fissure": [ + "HP:0100952" + ], + "enlarge interhemispheric fissure": [ + "HP:0100953" + ], + "enlarged interhemispheric fissure": [ + "HP:0100953" + ], + "enlarge great longitudinal fissure": [ + "HP:0100953" + ], + "enlarged great longitudinal fissure": [ + "HP:0100953" + ], + "enlarge longitudinal cerebral fissure": [ + "HP:0100953" + ], + "enlarged longitudinal cerebral fissure": [ + "HP:0100953" + ], + "enlarge longitudinal fissure": [ + "HP:0100953" + ], + "enlarged longitudinal fissure": [ + "HP:0100953" + ], + "open operculum": [ + "HP:0100954" + ], + "giant cell granuloma of mandible": [ + "HP:0100955" + ], + "abnormal renal medulla morphology": [ + "HP:0100957" + ], + "abnormality of the renal medulla": [ + "HP:0100957" + ], + "narrow foramen obturatorium": [ + "HP:0100958" + ], + "dense metaphyseal band": [ + "HP:0100959" + ], + "dense metaphyseal bands": [ + "HP:0100959" + ], + "dense metaphyseal line": [ + "HP:0100959" + ], + "dense metaphyseal lines": [ + "HP:0100959" + ], + "transverse metaphyseal band": [ + "HP:0100959" + ], + "transverse metaphyseal bands": [ + "HP:0100959" + ], + "asymmetric ventricle": [ + "HP:0100960" + ], + "asymmetric ventricles": [ + "HP:0100960" + ], + "enlarge hippocampus": [ + "HP:0100961" + ], + "enlarged hippocampus": [ + "HP:0100961" + ], + "shyness": [ + "HP:0100962" + ], + "hyperesthesia": [ + "HP:0100963" + ], + "hyperaesthesia": [ + "HP:0100963" + ], + "dysharmonic bone age": [ + "HP:0200000" + ], + "dysharmonic skeletal maturation": [ + "HP:0200000" + ], + "dysharmonic accelerate bone age": [ + "HP:0200001" + ], + "dysharmonic accelerated bone age": [ + "HP:0200001" + ], + "splay epiphysis": [ + "HP:0200003" + ], + "splayed epiphyses": [ + "HP:0200003" + ], + "splayed end part of bone": [ + "HP:0200003" + ], + "abnormal shape of the palpebral fissure": [ + "HP:0200005" + ], + "abnormal morphology of the palpebral fissure": [ + "HP:0200005" + ], + "abnormal shape of the opening between the eyelid": [ + "HP:0200005" + ], + "abnormal shape of the opening between the eyelids": [ + "HP:0200005" + ], + "slanting of the palpebral fissure": [ + "HP:0200006" + ], + "slanting of the opening between the eyelid": [ + "HP:0200006" + ], + "slanting of the opening between the eyelids": [ + "HP:0200006" + ], + "abnormal size of the palpebral fissure": [ + "HP:0200007" + ], + "abnormal size of the palpebral fissures": [ + "HP:0200007" + ], + "abnormal size of the eye": [ + "HP:0200007" + ], + "abnormal size of the eyes": [ + "HP:0200007" + ], + "abnormal size of the opening between the eyelid": [ + "HP:0200007" + ], + "abnormal size of the opening between the eyelids": [ + "HP:0200007" + ], + "intestinal polyposis": [ + "HP:0200008" + ], + "gastrointestinal polyp": [ + "HP:0200008" + ], + "gastrointestinal polyps": [ + "HP:0200008" + ], + "growth in inner lining of intestine": [ + "HP:0200008" + ], + "growths in inner lining of intestine": [ + "HP:0200008" + ], + "multiple intestinal polyp": [ + "HP:0200008" + ], + "multiple intestinal polyps": [ + "HP:0200008" + ], + "abnormal length of corpus callosum": [ + "HP:0200011" + ], + "short corpus callosum": [ + "HP:0200012" + ], + "neoplasm of fatty tissue": [ + "HP:0200013" + ], + "tumor of fatty tissue": [ + "HP:0200013" + ], + "tumour of fatty tissue": [ + "HP:0200013" + ], + "symmetric great toe depigmentation": [ + "HP:0200015" + ], + "acrokeratosis": [ + "HP:0200016" + ], + "acral keratosis": [ + "HP:0200016" + ], + "cerebral white matter agenesis": [ + "HP:0200017" + ], + "agenesis of the cerebral white matter": [ + "HP:0200017" + ], + "white matter agenesis": [ + "HP:0200017" + ], + "protanomaly": [ + "HP:0200018" + ], + "colorblindness , partial , protan series": [ + "HP:0200018" + ], + "red - weak": [ + "HP:0200018" + ], + "corneal erosion": [ + "HP:0200020" + ], + "damage to outer layer of the cornea of the eye": [ + "HP:0200020" + ], + "down - sloping shoulder": [ + "HP:0200021" + ], + "down - sloping shoulders": [ + "HP:0200021" + ], + "rounded shoulder": [ + "HP:0200021" + ], + "rounded shoulders": [ + "HP:0200021" + ], + "round , slop shoulder": [ + "HP:0200021" + ], + "rounded , sloping shoulders": [ + "HP:0200021" + ], + "slop shoulder": [ + "HP:0200021" + ], + "sloping shoulders": [ + "HP:0200021" + ], + "choroid plexus papilloma": [ + "HP:0200022" + ], + "priapism": [ + "HP:0200023" + ], + "hulseyism": [ + "HP:0200023" + ], + "premature chromatid separation": [ + "HP:0200024" + ], + "mandibular pain": [ + "HP:0200025" + ], + "low jaw pain": [ + "HP:0200025" + ], + "lower jaw pain": [ + "HP:0200025" + ], + "ocular pain": [ + "HP:0200026" + ], + "eye pain": [ + "HP:0200026" + ], + "pretibial myxedema": [ + "HP:0200028" + ], + "graf dermopathy": [ + "HP:0200028" + ], + "graves dermopathy": [ + "HP:0200028" + ], + "vasculitis in the skin": [ + "HP:0200029" + ], + "cutaneous vasculitis": [ + "HP:0200029" + ], + "punctate vasculitis skin lesion": [ + "HP:0200030" + ], + "punctate vasculitis skin lesions": [ + "HP:0200030" + ], + "kayser - fleischer ring": [ + "HP:0200032" + ], + "fleischer 's ring": [ + "HP:0200032" + ], + "fleischer - kayser ring": [ + "HP:0200032" + ], + "fleischer - struempell ring": [ + "HP:0200032" + ], + "papule": [ + "HP:0200034" + ], + "papules": [ + "HP:0200034" + ], + "skin papule": [ + "HP:0200034" + ], + "skin papules": [ + "HP:0200034" + ], + "skin plaque": [ + "HP:0200035" + ], + "skin nodule": [ + "HP:0200036" + ], + "growth of abnormal tissue on or under the skin": [ + "HP:0200036" + ], + "skin vesicle": [ + "HP:0200037" + ], + "pustule": [ + "HP:0200039" + ], + "pimple": [ + "HP:0200039" + ], + "pustula": [ + "HP:0200039" + ], + "pustular lesion": [ + "HP:0200039" + ], + "pustules": [ + "HP:0200039" + ], + "skin pustule": [ + "HP:0200039" + ], + "skin pustules": [ + "HP:0200039" + ], + "epidermoid cyst": [ + "HP:0200040" + ], + "epidermal cyst": [ + "HP:0200040" + ], + "epidermal inclusion cyst": [ + "HP:0200040" + ], + "epidermoid cysts": [ + "HP:0200040" + ], + "infundibular cyst": [ + "HP:0200040" + ], + "keratin cyst": [ + "HP:0200040" + ], + "sebaceous cyst": [ + "HP:0200040" + ], + "skin cyst": [ + "HP:0200040" + ], + "skin erosion": [ + "HP:0200041" + ], + "skin ulcer": [ + "HP:0200042" + ], + "open skin sore": [ + "HP:0200042" + ], + "verruca": [ + "HP:0200043" + ], + "verrucae": [ + "HP:0200043" + ], + "wart": [ + "HP:0200043" + ], + "warts": [ + "HP:0200043" + ], + "porokeratosis": [ + "HP:0200044" + ], + "cat cry": [ + "HP:0200046" + ], + "cat - like cry": [ + "HP:0200046" + ], + "cri de chat - associate cry": [ + "HP:0200046" + ], + "cri de chat - associated cry": [ + "HP:0200046" + ], + "chondritis of pinna": [ + "HP:0200047" + ], + "inflammation of cartilage of pinna": [ + "HP:0200047" + ], + "cyanotic episode": [ + "HP:0200048" + ], + "upper limb hypertonia": [ + "HP:0200049" + ], + "bracket metacarpal epiphysis": [ + "HP:0200050" + ], + "bracket metacarpal epiphyses": [ + "HP:0200050" + ], + "bracket shape end part of long bone of hand": [ + "HP:0200050" + ], + "bracket shaped end part of long bone of hand": [ + "HP:0200050" + ], + "hemihypotrophy of low limb": [ + "HP:0200053" + ], + "hemihypotrophy of lower limb": [ + "HP:0200053" + ], + "asymmetric leg shorten": [ + "HP:0200053" + ], + "asymmetric leg shortening": [ + "HP:0200053" + ], + "asymmetric low limb shortness": [ + "HP:0200053" + ], + "asymmetric lower limb shortness": [ + "HP:0200053" + ], + "foot monodactyly": [ + "HP:0200054" + ], + "small hand": [ + "HP:0200055" + ], + "disproportionately small hand": [ + "HP:0200055" + ], + "disproportionately small hands": [ + "HP:0200055" + ], + "small hands": [ + "HP:0200055" + ], + "macular scar": [ + "HP:0200056" + ], + "macular scarring": [ + "HP:0200056" + ], + "marcus gunn pupil": [ + "HP:0200057" + ], + "relative afferent pupil defect": [ + "HP:0200057" + ], + "relative afferent pupillary defect": [ + "HP:0200057" + ], + "angiosarcoma": [ + "HP:0200058" + ], + "metastatic angiosarcoma": [ + "HP:0200059" + ], + "colorectal polyposis": [ + "HP:0200063" + ], + "colorectal polyp": [ + "HP:0200063" + ], + "colorectal polyps": [ + "HP:0200063" + ], + "asymmetry of iris pigmentation": [ + "HP:0200064" + ], + "chorioretinal degeneration": [ + "HP:0200065" + ], + "ribbonlike corneal degeneration": [ + "HP:0200066" + ], + "recurrent spontaneous abortion": [ + "HP:0200067" + ], + "spontaneous abortion , recurrent": [ + "HP:0200067" + ], + "nonprogressive visual loss": [ + "HP:0200068" + ], + "decrease visual acuity , nonprogressive": [ + "HP:0200068" + ], + "decreased visual acuity , nonprogressive": [ + "HP:0200068" + ], + "peripheral retinal atrophy": [ + "HP:0200070" + ], + "wasting of the out part of the retina": [ + "HP:0200070" + ], + "wasting of the outer part of the retina": [ + "HP:0200070" + ], + "peripheral vitreoretinal degeneration": [ + "HP:0200071" + ], + "episodic quadriplegia": [ + "HP:0200072" + ], + "quadriplegia , episodic": [ + "HP:0200072" + ], + "respiratory insufficiency due to defective ciliary clearance": [ + "HP:0200073" + ], + "severe limb shorten": [ + "HP:0200083" + ], + "severe limb shortening": [ + "HP:0200083" + ], + "giant cell hepatitis": [ + "HP:0200084" + ], + "giant cell hepatitis on biopsy": [ + "HP:0200084" + ], + "giant cell hepatitis on liver biopsy": [ + "HP:0200084" + ], + "giant cell hepatitis show on biopsy": [ + "HP:0200084" + ], + "giant cell hepatitis shown on biopsy": [ + "HP:0200084" + ], + "limb tremor": [ + "HP:0200085" + ], + "involuntary shaking of limb": [ + "HP:0200085" + ], + "tremor of limb": [ + "HP:0200085" + ], + "tremor of limbs": [ + "HP:0200085" + ], + "frontal open bite": [ + "HP:0200094" + ], + "obsolete anterior open bite": [ + "HP:0200095" + ], + "triangular - shape open mouth": [ + "HP:0200096" + ], + "triangular - shaped open mouth": [ + "HP:0200096" + ], + "oral mucosal blister": [ + "HP:0200097" + ], + "oral mucosal blisters": [ + "HP:0200097" + ], + "bleb of oral mucosa": [ + "HP:0200097" + ], + "blebs of oral mucosa": [ + "HP:0200097" + ], + "blister of mouth": [ + "HP:0200097" + ], + "blisters of mouth": [ + "HP:0200097" + ], + "bulla of oral mucosa": [ + "HP:0200097" + ], + "bullae of oral mucosa": [ + "HP:0200097" + ], + "oral blistering": [ + "HP:0200097" + ], + "oral mucosa blister": [ + "HP:0200097" + ], + "oral mucosa blisters": [ + "HP:0200097" + ], + "absent skin pigmentation": [ + "HP:0200098" + ], + "lack of skin coloration": [ + "HP:0200098" + ], + "obsolete peripheral retinal pigmentation abnormality": [ + "HP:0200099" + ], + "obsolete peripheral retinal pigmentation abnormalities": [ + "HP:0200099" + ], + "decrease / absent ankle reflex": [ + "HP:0200101" + ], + "decreased / absent ankle reflexes": [ + "HP:0200101" + ], + "decrease or absent ankle reflex": [ + "HP:0200101" + ], + "decreased or absent ankle reflexes": [ + "HP:0200101" + ], + "sparse or absent eyelash": [ + "HP:0200102" + ], + "sparse or absent eyelashes": [ + "HP:0200102" + ], + "partial to total absence of eyelash": [ + "HP:0200102" + ], + "partial to total absence of eyelashes": [ + "HP:0200102" + ], + "sparse to absent eyelash": [ + "HP:0200102" + ], + "sparse to absent eyelashes": [ + "HP:0200102" + ], + "absent fifth fingernail": [ + "HP:0200104" + ], + "absent nail of fifth finger": [ + "HP:0200104" + ], + "absent fifth toenail": [ + "HP:0200105" + ], + "miss fifth toenail": [ + "HP:0200105" + ], + "missing fifth toenail": [ + "HP:0200105" + ], + "absent / shorten dynein arm": [ + "HP:0200106" + ], + "absent / shortened dynein arms": [ + "HP:0200106" + ], + "shorten inner dynein arm": [ + "HP:0200107" + ], + "shortened inner dynein arms": [ + "HP:0200107" + ], + "shorten out dynein arm": [ + "HP:0200108" + ], + "shortened outer dynein arms": [ + "HP:0200108" + ], + "absent / shorten out dynein arm": [ + "HP:0200109" + ], + "absent / shortened outer dynein arms": [ + "HP:0200109" + ], + "respiratory cilium have shorten or absent outer dynein arm": [ + "HP:0200109" + ], + "respiratory cilia have shortened or absent outer dynein arms": [ + "HP:0200109" + ], + "absent stapes head": [ + "HP:0200111" + ], + "aphalangy of hand and foot": [ + "HP:0200113" + ], + "aphalangy of hands and feet": [ + "HP:0200113" + ], + "aphalangy , hand and foot": [ + "HP:0200113" + ], + "aphalangy , hands and feet": [ + "HP:0200113" + ], + "metabolic alkalosis": [ + "HP:0200114" + ], + "distal ileal atresia": [ + "HP:0200116" + ], + "recurrent upper and low respiratory tract infection": [ + "HP:0200117" + ], + "recurrent upper and lower respiratory tract infections": [ + "HP:0200117" + ], + "malabsorption of vitamin b12": [ + "HP:0200118" + ], + "malabsorption of cyanocobalamin": [ + "HP:0200118" + ], + "vitamin b12 deficiency cause by intestinal malabsorption": [ + "HP:0200118" + ], + "vitamin b12 deficiency caused by intestinal malabsorption": [ + "HP:0200118" + ], + "acute hepatitis": [ + "HP:0200119" + ], + "acute liver inflammation": [ + "HP:0200119" + ], + "chronic active hepatitis": [ + "HP:0200120" + ], + "hepatitis , chronic active": [ + "HP:0200120" + ], + "atypical or prolonged hepatitis": [ + "HP:0200122" + ], + "atypical or prolonged liver inflammation": [ + "HP:0200122" + ], + "chronic hepatitis": [ + "HP:0200123" + ], + "chronic liver inflammation": [ + "HP:0200123" + ], + "chronic hepatitis due to cryptosporidium infection": [ + "HP:0200124" + ], + "hepatitis , chronic , due to cryptosporidium infection": [ + "HP:0200124" + ], + "mitochondrial respiratory chain defect": [ + "HP:0200125" + ], + "mitochondrial respiratory chain defects": [ + "HP:0200125" + ], + "obsolete amyloid cardiomyopathy": [ + "HP:0200126" + ], + "atrial cardiomyopathy": [ + "HP:0200127" + ], + "biventricular hypertrophy": [ + "HP:0200128" + ], + "obsolete calcific mitral stenosis": [ + "HP:0200129" + ], + "lumbosacral meningocele": [ + "HP:0200133" + ], + "epileptic encephalopathy": [ + "HP:0200134" + ], + "convulsive encephalopathy": [ + "HP:0200134" + ], + "obsolete macrocephaly due to hydrocephalus": [ + "HP:0200135" + ], + "oral - pharyngeal dysphagia": [ + "HP:0200136" + ], + "oral pharyngeal dysphagia": [ + "HP:0200136" + ], + "oropharyngeal dysphagia": [ + "HP:0200136" + ], + "bilateral choanal atresia / stenosis": [ + "HP:0200138" + ], + "small , conical teeth": [ + "HP:0200141" + ], + "conical microdontia": [ + "HP:0200141" + ], + "small , cone shape teeth": [ + "HP:0200141" + ], + "small , cone shaped teeth": [ + "HP:0200141" + ], + "small , peg shape teeth": [ + "HP:0200141" + ], + "small , peg shaped teeth": [ + "HP:0200141" + ], + "small , point teeth": [ + "HP:0200141" + ], + "small , pointed teeth": [ + "HP:0200141" + ], + "megaloblastic erythroid hyperplasia": [ + "HP:0200143" + ], + "bone marrow biopsy show megaloblastic erythroid hyperplasia": [ + "HP:0200143" + ], + "bone marrow biopsy shows megaloblastic erythroid hyperplasia": [ + "HP:0200143" + ], + "obsolete anaphylactoid purpura": [ + "HP:0200144" + ], + "mucoid extracellular matrix accumulation": [ + "HP:0200146" + ], + "cystic medial necrosis of the aorta": [ + "HP:0200146" + ], + "neuronal loss in basal ganglion": [ + "HP:0200147" + ], + "neuronal loss in basal ganglia": [ + "HP:0200147" + ], + "abnormal liver function test during pregnancy": [ + "HP:0200148" + ], + "abnormal liver function tests during pregnancy": [ + "HP:0200148" + ], + "abnormal liver function test during pregnancy , resolve postpartum": [ + "HP:0200148" + ], + "abnormal liver function tests during pregnancy , resolves postpartum": [ + "HP:0200148" + ], + "csf lymphocytic pleiocytosis": [ + "HP:0200149" + ], + "csf lymphocytosis": [ + "HP:0200149" + ], + "increase serum bile acid concentration during pregnancy": [ + "HP:0200150" + ], + "increased serum bile acid concentration during pregnancy": [ + "HP:0200150" + ], + "increase serum bile acid concentration during pregnancy , resolve": [ + "HP:0200150" + ], + "increased serum bile acid concentration during pregnancy , resolves": [ + "HP:0200150" + ], + "cutaneous mastocytosis": [ + "HP:0200151" + ], + "agenesis of lateral incisor": [ + "HP:0200153" + ], + "absence of lateral incisor": [ + "HP:0200153" + ], + "failure of development of lateral incisor": [ + "HP:0200153" + ], + "miss lateral incisor": [ + "HP:0200153" + ], + "missing lateral incisor": [ + "HP:0200153" + ], + "agenesis of mandibular lateral incisor": [ + "HP:0200154" + ], + "absence of low lateral incisor": [ + "HP:0200154" + ], + "absence of lower lateral incisor": [ + "HP:0200154" + ], + "absence of mandibular lateral incisor": [ + "HP:0200154" + ], + "failure of development of mandibular lateral incisor": [ + "HP:0200154" + ], + "miss low lateral incisor": [ + "HP:0200154" + ], + "missing lower lateral incisor": [ + "HP:0200154" + ], + "miss mandibular lateral incisor": [ + "HP:0200154" + ], + "missing mandibular lateral incisor": [ + "HP:0200154" + ], + "agenesis of permanent mandibular lateral incisor": [ + "HP:0200158" + ], + "absence of adult mandibular lateral incisor": [ + "HP:0200158" + ], + "absence of permanent mandibular lateral incisor": [ + "HP:0200158" + ], + "failure of development of permanent mandibular lateral incisor": [ + "HP:0200158" + ], + "miss adult lower lateral incisor": [ + "HP:0200158" + ], + "missing adult lower lateral incisor": [ + "HP:0200158" + ], + "miss permanent mandibular lateral incisor": [ + "HP:0200158" + ], + "missing permanent mandibular lateral incisor": [ + "HP:0200158" + ], + "agenesis of primary mandibular lateral incisor": [ + "HP:0200159" + ], + "absence of deciduous mandibular lateral incisor": [ + "HP:0200159" + ], + "absence of low front baby tooth": [ + "HP:0200159" + ], + "absence of lower front baby tooth": [ + "HP:0200159" + ], + "absence of primary mandibular lateral incisor": [ + "HP:0200159" + ], + "agenesis of deciduous mandibular lateral incisor": [ + "HP:0200159" + ], + "failure of development of deciduous mandibular lateral incisor": [ + "HP:0200159" + ], + "failure of development of primary mandibular lateral incisor": [ + "HP:0200159" + ], + "miss deciduous mandibular lateral incisor": [ + "HP:0200159" + ], + "missing deciduous mandibular lateral incisor": [ + "HP:0200159" + ], + "miss primary mandibular lateral incisor": [ + "HP:0200159" + ], + "missing primary mandibular lateral incisor": [ + "HP:0200159" + ], + "agenesis of maxillary incisor": [ + "HP:0200160" + ], + "absence of maxillary incisor": [ + "HP:0200160" + ], + "absence of upper front tooth": [ + "HP:0200160" + ], + "failure of development of maxillary incisor": [ + "HP:0200160" + ], + "failure of development of upper incisor": [ + "HP:0200160" + ], + "miss upper front tooth": [ + "HP:0200160" + ], + "missing upper front tooth": [ + "HP:0200160" + ], + "miss upper incisor": [ + "HP:0200160" + ], + "missing upper incisor": [ + "HP:0200160" + ], + "agenesis of mandibular incisor": [ + "HP:0200161" + ], + "absence of low front tooth": [ + "HP:0200161" + ], + "absence of lower front tooth": [ + "HP:0200161" + ], + "absence of low incisor": [ + "HP:0200161" + ], + "absence of lower incisor": [ + "HP:0200161" + ], + "absence of mandibular incisor": [ + "HP:0200161" + ], + "agenesis of low incisor": [ + "HP:0200161" + ], + "agenesis of lower incisor": [ + "HP:0200161" + ], + "failure of development of mandibular incisor": [ + "HP:0200161" + ], + "miss low front tooth": [ + "HP:0200161" + ], + "missing lower front tooth": [ + "HP:0200161" + ], + "miss low incisor": [ + "HP:0200161" + ], + "missing lower incisor": [ + "HP:0200161" + ], + "tall chin": [ + "HP:0400000" + ], + "increase height of chin": [ + "HP:0400000" + ], + "increased height of chin": [ + "HP:0400000" + ], + "increase height of menton region": [ + "HP:0400000" + ], + "increased height of menton region": [ + "HP:0400000" + ], + "long chin": [ + "HP:0400000" + ], + "long low third of face": [ + "HP:0400000" + ], + "long lower third of face": [ + "HP:0400000" + ], + "vertical excess of chin": [ + "HP:0400000" + ], + "vertical hyperplasia of chin": [ + "HP:0400000" + ], + "chin with vertical crease": [ + "HP:0400001" + ], + "chin with vertical furrow": [ + "HP:0400001" + ], + "chin with vertical groove": [ + "HP:0400001" + ], + "chin with vertical sulcus": [ + "HP:0400001" + ], + "chin , vertical crease": [ + "HP:0400001" + ], + "cleft chin": [ + "HP:0400001" + ], + "vertical chin skin cleft": [ + "HP:0400001" + ], + "vertical menton crease": [ + "HP:0400001" + ], + "extra concha fold": [ + "HP:0400002" + ], + "concha , extra fold": [ + "HP:0400002" + ], + "focal absence of the external ear": [ + "HP:0400003" + ], + "long ear": [ + "HP:0400004" + ], + "long ears": [ + "HP:0400004" + ], + "short ear": [ + "HP:0400005" + ], + "short ears": [ + "HP:0400005" + ], + "polymenorrhea": [ + "HP:0400007" + ], + "menometrorrhagia": [ + "HP:0400008" + ], + "abnormality of vomer": [ + "HP:0410000" + ], + "abnormality of vomer bone": [ + "HP:0410000" + ], + "defect of vomer": [ + "HP:0410000" + ], + "cleft maxillary alveolus": [ + "HP:0410003" + ], + "alveolar cleft": [ + "HP:0410003" + ], + "cleft alveolar process of maxilla": [ + "HP:0410003" + ], + "cleft anterior maxilla": [ + "HP:0410003" + ], + "cleft primary palate": [ + "HP:0410003" + ], + "obsolete cleft secondary palate": [ + "HP:0410004" + ], + "cleft hard palate": [ + "HP:0410005" + ], + "cleft bony palate": [ + "HP:0410005" + ], + "cleft of hard palate": [ + "HP:0410005" + ], + "abnormality of ophthalmic artery": [ + "HP:0410006" + ], + "ophthalmic artery anomaly": [ + "HP:0410006" + ], + "obsolete abnormality of cartilage morphology": [ + "HP:0410007" + ], + "abnormality of the peripheral nervous system": [ + "HP:0410008" + ], + "abnormality of the somatic nervous system": [ + "HP:0410009" + ], + "abnormality of somatic nerve plexus": [ + "HP:0410010" + ], + "abnormality of masticatory muscle": [ + "HP:0410011" + ], + "abnormality of muscle of mastication": [ + "HP:0410011" + ], + "abnormality of muscles of mastication": [ + "HP:0410011" + ], + "abnormal mouth floor morphology": [ + "HP:0410012" + ], + "abnormality of the floor of mouth": [ + "HP:0410012" + ], + "abnormality of the mouth floor": [ + "HP:0410012" + ], + "abnormality of the submandibular region": [ + "HP:0410013" + ], + "abnormality of ganglion": [ + "HP:0410014" + ], + "abnormality of ganglion of peripheral nervous system": [ + "HP:0410015" + ], + "abnormality of cranial ganglion": [ + "HP:0410016" + ], + "otitis externa": [ + "HP:0410017" + ], + "swimmer 's ear": [ + "HP:0410017" + ], + "recurrent ear infection": [ + "HP:0410018" + ], + "recurrent ear infections": [ + "HP:0410018" + ], + "frequent ear infection": [ + "HP:0410018" + ], + "frequent ear infections": [ + "HP:0410018" + ], + "epigastric pain": [ + "HP:0410019" + ], + "epigastrium pain": [ + "HP:0410019" + ], + "fish odor": [ + "HP:0410020" + ], + "fish odour": [ + "HP:0410020" + ], + "fishy body odor": [ + "HP:0410020" + ], + "fishy body odour": [ + "HP:0410020" + ], + "fishy odor": [ + "HP:0410020" + ], + "fishy odour": [ + "HP:0410020" + ], + "musty odor": [ + "HP:0410021" + ], + "musty odour": [ + "HP:0410021" + ], + "vaginal fish odor": [ + "HP:0410022" + ], + "vaginal fish odour": [ + "HP:0410022" + ], + "abnormal distribution of cell junction proteins in buccal mucosal cell": [ + "HP:0410023" + ], + "abnormal distribution of cell junction proteins in buccal mucosal cells": [ + "HP:0410023" + ], + "abnormal periodontium morphology": [ + "HP:0410026" + ], + "abnormality of the periodontium": [ + "HP:0410026" + ], + "alveolar bone loss around teeth": [ + "HP:0410027" + ], + "bone loss around teeth": [ + "HP:0410027" + ], + "recurrent oral herpes": [ + "HP:0410028" + ], + "recurrent herpes labialis": [ + "HP:0410028" + ], + "cleft lip": [ + "HP:0410030" + ], + "cleft of the lip": [ + "HP:0410030" + ], + "submucous cleft of soft and hard palate": [ + "HP:0410031" + ], + "obsolete cleft of uvula": [ + "HP:0410032" + ], + "unilateral alveolar cleft of maxilla": [ + "HP:0410033" + ], + "bilateral alveolar cleft of maxilla": [ + "HP:0410034" + ], + "abnormal t cell activation": [ + "HP:0410035" + ], + "abnormal t lymphocyte activation": [ + "HP:0410035" + ], + "abnormal t - cell activation": [ + "HP:0410035" + ], + "abnormal t - lymphocyte activation": [ + "HP:0410035" + ], + "abnormal liver morphology": [ + "HP:0410042" + ], + "abnormal neural tube morphology": [ + "HP:0410043" + ], + "abnormality of radial ray": [ + "HP:0410049" + ], + "deformity of radial ray": [ + "HP:0410049" + ], + "radial ray abnormality": [ + "HP:0410049" + ], + "radial ray anomaly": [ + "HP:0410049" + ], + "radial ray deformity": [ + "HP:0410049" + ], + "decrease level of 1,5 anhydroglucitol in serum": [ + "HP:0410050" + ], + "decreased level of 1,5 anhydroglucitol in serum": [ + "HP:0410050" + ], + "decrease level of 1,5 - ag in serum": [ + "HP:0410050" + ], + "decreased level of 1,5 - ag in serum": [ + "HP:0410050" + ], + "decrease level of 1,5 - anhydro - d - glucitol in serum": [ + "HP:0410050" + ], + "decreased level of 1,5 - anhydro - d - glucitol in serum": [ + "HP:0410050" + ], + "decrease level of 1,5 - anhydroglucitol in serum": [ + "HP:0410050" + ], + "decreased level of 1,5 - anhydroglucitol in serum": [ + "HP:0410050" + ], + "increase level of 3 - hydroxy - 3 - methylglutaric acid in urine": [ + "HP:0410051" + ], + "increased level of 3 - hydroxy - 3 - methylglutaric acid in urine": [ + "HP:0410051" + ], + "increase level of allantoin in serum": [ + "HP:0410052" + ], + "increased level of allantoin in serum": [ + "HP:0410052" + ], + "elevate circulate gamma - aminobutyric acid concentration": [ + "HP:0410053" + ], + "elevated circulating gamma - aminobutyric acid concentration": [ + "HP:0410053" + ], + "increase circulate gaba concentration": [ + "HP:0410053" + ], + "increased circulating gaba concentration": [ + "HP:0410053" + ], + "increase level of gaba in serum": [ + "HP:0410053" + ], + "increased level of gaba in serum": [ + "HP:0410053" + ], + "increase level of gamma - aminobutyric acid in serum": [ + "HP:0410053" + ], + "increased level of gamma - aminobutyric acid in serum": [ + "HP:0410053" + ], + "decrease circulate gaba concentration": [ + "HP:0410054" + ], + "decreased circulating gaba concentration": [ + "HP:0410054" + ], + "decrease level of gamma - aminobutyric acid in serum": [ + "HP:0410054" + ], + "decreased level of gamma - aminobutyric acid in serum": [ + "HP:0410054" + ], + "decrease level of erythritol in urine": [ + "HP:0410055" + ], + "decreased level of erythritol in urine": [ + "HP:0410055" + ], + "decrease level of erythritol in csf": [ + "HP:0410056" + ], + "decreased level of erythritol in csf": [ + "HP:0410056" + ], + "decrease level of erythritol in cerebrospinal fluid": [ + "HP:0410056" + ], + "decreased level of erythritol in cerebrospinal fluid": [ + "HP:0410056" + ], + "increase level of d - threitol in plasma": [ + "HP:0410057" + ], + "increased level of d - threitol in plasma": [ + "HP:0410057" + ], + "increase level of d - threitol in csf": [ + "HP:0410058" + ], + "increased level of d - threitol in csf": [ + "HP:0410058" + ], + "increase level of d - threitol in cerebrospinal fluid": [ + "HP:0410058" + ], + "increased level of d - threitol in cerebrospinal fluid": [ + "HP:0410058" + ], + "increase level of d - threitol in urine": [ + "HP:0410059" + ], + "increased level of d - threitol in urine": [ + "HP:0410059" + ], + "decrease level of d - mannose in urine": [ + "HP:0410060" + ], + "decreased level of d - mannose in urine": [ + "HP:0410060" + ], + "increase level of galactitol in plasma": [ + "HP:0410061" + ], + "increased level of galactitol in plasma": [ + "HP:0410061" + ], + "increase level of galactitol in urine": [ + "HP:0410062" + ], + "increased level of galactitol in urine": [ + "HP:0410062" + ], + "increase level of galactonate in red blood cell": [ + "HP:0410063" + ], + "increased level of galactonate in red blood cells": [ + "HP:0410063" + ], + "increase level of galactonate in erythrocyte": [ + "HP:0410063" + ], + "increased level of galactonate in erythrocytes": [ + "HP:0410063" + ], + "increase level of galactonate in rbc": [ + "HP:0410063" + ], + "increased level of galactonate in rbcs": [ + "HP:0410063" + ], + "increase level of galactitol in red blood cell": [ + "HP:0410064" + ], + "increased level of galactitol in red blood cells": [ + "HP:0410064" + ], + "increase level of galactitol in erythrocyte": [ 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gal allergy": [ + "HP:0410319" + ], + "animal protein allergy": [ + "HP:0410320" + ], + "allergy to animal protein": [ + "HP:0410320" + ], + "allergy to animal proteins": [ + "HP:0410320" + ], + "ige - mediate animal protein allergy": [ + "HP:0410320" + ], + "ige - mediated animal protein allergy": [ + "HP:0410320" + ], + "immunoglobulin e - mediate animal protein allergy": [ + "HP:0410320" + ], + "immunoglobulin e - mediated animal protein allergy": [ + "HP:0410320" + ], + "animal dander allergy": [ + "HP:0410321" + ], + "allergy to animal dander": [ + "HP:0410321" + ], + "ige - mediate animal dander allergy": [ + "HP:0410321" + ], + "ige - mediated animal dander allergy": [ + "HP:0410321" + ], + "immunoglobulin e - mediate animal dander allergy": [ + "HP:0410321" + ], + "immunoglobulin e - mediated animal dander allergy": [ + "HP:0410321" + ], + "bacteria allergy": [ + "HP:0410322" + ], + "allergy to bacteria": [ + "HP:0410322" + ], + "ige - mediate bacteria allergy": [ + 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"house dust mite allergy": [ + "HP:0410325" + ], + "allergy to house dust mite": [ + "HP:0410325" + ], + "allergy to house dust mites": [ + "HP:0410325" + ], + "ige - mediate house dust mite allergy": [ + "HP:0410325" + ], + "ige - mediated house dust mite allergy": [ + "HP:0410325" + ], + "immunoglobulin e - mediate house dust mite allergy": [ + "HP:0410325" + ], + "immunoglobulin e - mediated house dust mite allergy": [ + "HP:0410325" + ], + "feather allergy": [ + "HP:0410326" + ], + "allergy to feather": [ + "HP:0410326" + ], + "allergy to feathers": [ + "HP:0410326" + ], + "ige - mediate feather allergy": [ + "HP:0410326" + ], + "ige - mediated feather allergy": [ + "HP:0410326" + ], + "immunoglobulin e - mediate feather allergy": [ + "HP:0410326" + ], + "immunoglobulin e - mediated feather allergy": [ + "HP:0410326" + ], + "dairy allergy": [ + "HP:0410327" + ], + "allergy to dairy": [ + "HP:0410327" + ], + "ige - mediate dairy allergy": [ + "HP:0410327" + ], + "ige - mediated 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fungi allergy": [ + "HP:0410334" + ], + "immunoglobulin e - mediate fungi allergy": [ + "HP:0410334" + ], + "immunoglobulin e - mediated fungi allergy": [ + "HP:0410334" + ], + "insect allergy": [ + "HP:0410335" + ], + "allergy to insect": [ + "HP:0410335" + ], + "allergy to insects": [ + "HP:0410335" + ], + "ige - mediate insect allergy": [ + "HP:0410335" + ], + "ige - mediated insect allergy": [ + "HP:0410335" + ], + "immunoglobulin e - mediate insect allergy": [ + "HP:0410335" + ], + "immunoglobulin e - mediated insect allergy": [ + "HP:0410335" + ], + "venom allergy": [ + "HP:0410336" + ], + "allergy to venom": [ + "HP:0410336" + ], + "ige - mediate venom allergy": [ + "HP:0410336" + ], + "ige - mediated venom allergy": [ + "HP:0410336" + ], + "immunoglobulin e - mediate venom allergy": [ + "HP:0410336" + ], + "immunoglobulin e - mediated venom allergy": [ + "HP:0410336" + ], + "parasite allergy": [ + "HP:0410337" + ], + "allergy to parasite": [ + "HP:0410337" + ], + "allergy to parasites": [ + "HP:0410337" + ], + "ige - mediate parasite allergy": [ + "HP:0410337" + ], + "ige - mediated parasite allergy": [ + "HP:0410337" + ], + "immunoglobulin e - mediate parasite allergy": [ + "HP:0410337" + ], + "immunoglobulin e - mediated parasite allergy": [ + "HP:0410337" + ], + "plant product allergy": [ + "HP:0410338" + ], + "allergy to plant product": [ + "HP:0410338" + ], + "allergy to plant products": [ + "HP:0410338" + ], + "ige - mediate plant product allergy": [ + "HP:0410338" + ], + "ige - mediated plant product allergy": [ + "HP:0410338" + ], + "immunoglobulin e - mediate plant product allergy": [ + "HP:0410338" + ], + "immunoglobulin e - mediated plant product allergy": [ + "HP:0410338" + ], + "insect bite allergy": [ + "HP:0410339" + ], + "allergy to insect bite": [ + "HP:0410339" + ], + "allergy to insect bites": [ + "HP:0410339" + ], + "ige - mediate insect bite allergy": [ + "HP:0410339" + ], + "ige - mediated insect bite allergy": [ + "HP:0410339" + ], + 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concentration": [ + "HP:0410342" + ], + "increased blood heparan sulfate concentration": [ + "HP:0410342" + ], + "increase blood heparan sulphate concentration": [ + "HP:0410342" + ], + "increased blood heparan sulphate concentration": [ + "HP:0410342" + ], + "increase circulate heparan sulphate level": [ + "HP:0410342" + ], + "increased circulating heparan sulphate level": [ + "HP:0410342" + ], + "decrease circulate heparan sulfate level": [ + "HP:0410343" + ], + "decreased circulating heparan sulfate level": [ + "HP:0410343" + ], + "decrease blood heparan sulfate concentration": [ + "HP:0410343" + ], + "decreased blood heparan sulfate concentration": [ + "HP:0410343" + ], + "decrease blood heparan sulphate concentration": [ + "HP:0410343" + ], + "decreased blood heparan sulphate concentration": [ + "HP:0410343" + ], + "decrease circulate heparan sulphate level": [ + "HP:0410343" + ], + "decreased circulating heparan sulphate level": [ + "HP:0410343" + ], + "shorten o - fucosylated 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type oligosaccharide in urine": [ + "HP:0410347" + ], + "increased concentration of high - mannose - type oligosaccharides in urine": [ + "HP:0410347" + ], + "increase urinary multiantennary sialylated oligosaccharide": [ + "HP:0410348" + ], + "increased urinary multiantennary sialylated oligosaccharide": [ + "HP:0410348" + ], + "increase concentration of multiantennary sialylated oligosaccharide in urine": [ + "HP:0410348" + ], + "increase concentration of multiantennary sialylated oligosaccharides in urine": [ + "HP:0410348" + ], + "decreased glycosyltransferase o - fucosylpeptide 3 - beta - n - acetylglucosaminyltransferase level": [ + "HP:0410349" + ], + "increase urinary fucosylated oligosaccharide": [ + "HP:0410350" + ], + "increased urinary fucosylated oligosaccharide": [ + "HP:0410350" + ], + "increase concentration of fucosylated oligosaccharide in urine": [ + "HP:0410350" + ], + "increased concentration of fucosylated oligosaccharides in urine": [ + "HP:0410350" + ], + 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"HP:0410358" + ], + "decreased high - mannose n - glycan level": [ + "HP:0410358" + ], + "decrease high - mannose n - glycans on glycoprotein concentration": [ + "HP:0410358" + ], + "decreased high - mannose n - glycans on glycoprotein concentration": [ + "HP:0410358" + ], + "abnormal core 1 o - glycan level": [ + "HP:0410359" + ], + "abnormal concentration of t - antigen": [ + "HP:0410359" + ], + "increase core 1 o - glycan level": [ + "HP:0410360" + ], + "increased core 1 o - glycan level": [ + "HP:0410360" + ], + "increase t - antigen concentration": [ + "HP:0410360" + ], + "increased t - antigen concentration": [ + "HP:0410360" + ], + "decrease core 1 o - glycan level": [ + "HP:0410361" + ], + "decreased core 1 o - glycan level": [ + "HP:0410361" + ], + "decrease t - antigen concentration": [ + "HP:0410361" + ], + "decreased t - antigen concentration": [ + "HP:0410361" + ], + "decrease o - mannosyl glycans on alpha - dystroglycan": [ + "HP:0410362" + ], + "decreased o - mannosyl glycans on alpha - dystroglycan": [ + "HP:0410362" + ], + "reduce o - mannosyl glycans on alpha - dystroglycan": [ + "HP:0410362" + ], + "reduced o - mannosyl glycans on alpha - dystroglycan": [ + "HP:0410362" + ], + "increase monosialylated core 1 o - glycan level": [ + "HP:0410363" + ], + "increased monosialylated core 1 o - glycan level": [ + "HP:0410363" + ], + "increase sialyl t - antigen concentration": [ + "HP:0410363" + ], + "increased sialyl t - antigen concentration": [ + "HP:0410363" + ], + "decrease monosialylated core 1 o - glycan level": [ + "HP:0410364" + ], + "decreased monosialylated core 1 o - glycan level": [ + "HP:0410364" + ], + "decrease sialyl t - antigen concentration": [ + "HP:0410364" + ], + "decreased sialyl t - antigen concentration": [ + "HP:0410364" + ], + "increase disialylated core 1 o - glycan level": [ + "HP:0410365" + ], + "increased disialylated core 1 o - glycan level": [ + "HP:0410365" + ], + "increase disialyl t - antigen concentration": [ + 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virus antibody level": [ + "HP:0410371" + ], + "increase tn - antigen level": [ + "HP:0410372" + ], + "increased tn - antigen level": [ + "HP:0410372" + ], + "increase o - galnac on glycoprotein concentration": [ + "HP:0410372" + ], + "increased o - galnac on glycoprotein concentration": [ + "HP:0410372" + ], + "abnormal proportion of naive cd4 t cell": [ + "HP:0410373" + ], + "abnormal proportion of naive cd4 t cells": [ + "HP:0410373" + ], + "abnormal proportion of cd4+cd45ra+ cell": [ + "HP:0410373" + ], + "abnormal proportion of cd4+cd45ra+ cells": [ + "HP:0410373" + ], + "abnormal proportion of naive thymus - derive cd4 - positive , alpha - beta t cell": [ + "HP:0410373" + ], + "abnormal proportion of naive thymus - derived cd4 - positive , alpha - beta t cells": [ + "HP:0410373" + ], + "abnormal proportion of naive cd8 t cell": [ + "HP:0410374" + ], + "abnormal proportion of naive cd8 t cells": [ + "HP:0410374" + ], + "increase proportion of naive cd4 t cell": [ + "HP:0410375" + 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proportion of effector memory cd8 - positive , alpha - beta t cell": [ + "HP:0410390" + ], + "decreased proportion of effector memory cd8 - positive , alpha - beta t cells": [ + "HP:0410390" + ], + "increase proportion of cd4 - positive , alpha - beta memory t cell": [ + "HP:0410391" + ], + "increased proportion of cd4 - positive , alpha - beta memory t cells": [ + "HP:0410391" + ], + "increase proportion of cd8 - positive , alpha - beta memory t cell": [ + "HP:0410392" + ], + "increased proportion of cd8 - positive , alpha - beta memory t cells": [ + "HP:0410392" + ], + "increase proportion of central memory cd4 - positive , alpha - beta t cell": [ + "HP:0410393" + ], + "increased proportion of central memory cd4 - positive , alpha - beta t cells": [ + "HP:0410393" + ], + "elevate proportion central memory cd4 - positive , alpha - beta t cell": [ + "HP:0410393" + ], + "elevated proportion central memory cd4 - positive , alpha - beta t cells": [ + "HP:0410393" + ], + "elevate proportion of cd4+ central memory cell": [ + "HP:0410393" + ], + "elevated proportion of cd4+ central memory cells": [ + "HP:0410393" + ], + "increase proportion of cd4+ central memory cell": [ + "HP:0410393" + ], + "increased proportion of cd4+ central memory cells": [ + "HP:0410393" + ], + "increase proportion of central memory cd4+ , alpha - beta t cell": [ + "HP:0410393" + ], + "increased proportion of central memory cd4+ , alpha - beta t cell": [ + "HP:0410393" + ], + "increase proportion of effector memory cd4 - positive , alpha - beta t cell": [ + "HP:0410394" + ], + "increased proportion of effector memory cd4 - positive , alpha - beta t cells": [ + "HP:0410394" + ], + "increase proportion of effector memory cd8 - positive , alpha - beta t cell": [ + "HP:0410395" + ], + "increased proportion of effector memory cd8 - positive , alpha - beta t cells": [ + "HP:0410395" + ], + "increase proportion of central memory cd8 - positive , alpha - beta t cell": [ + "HP:0410396" + ], + "increased proportion of central memory cd8 - positive , alpha - beta t cells": [ + "HP:0410396" + ], + "bronchiolectasis": [ + "HP:0410397" + ], + "bronchiolectasia": [ + "HP:0410397" + ], + "positive blood lead test": [ + "HP:0410399" + ], + "increase blood lead level": [ + "HP:0410399" + ], + "increased blood lead level": [ + "HP:0410399" + ], + "absent sebaceous gland": [ + "HP:0410400" + ], + "absent sebaceous glands": [ + "HP:0410400" + ], + "absence of sebaceous gland": [ + "HP:0410400" + ], + "absence of sebaceous glands": [ + "HP:0410400" + ], + "bad in evening": [ + "HP:0410401" + ], + "worse in evening": [ + "HP:0410401" + ], + "abnormality of the frontal bone": [ + "HP:0430000" + ], + "abnormal morphology of frontal bone": [ + "HP:0430000" + ], + "abnormality of the bone of the forehead": [ + "HP:0430000" + ], + "anomaly of the frontal bone": [ + "HP:0430000" + ], + "deformity of the frontal bone": [ + "HP:0430000" + ], + "malformation of the frontal bone": [ + "HP:0430000" 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"HP:0430007" + ], + "accessory eyelid": [ + "HP:0430008" + ], + "double eyelid": [ + "HP:0430008" + ], + "extra eyelid": [ + "HP:0430008" + ], + "hypoplasia of eyelid": [ + "HP:0430009" + ], + "decreased size of eyelid": [ + "HP:0430009" + ], + "short eyelid": [ + "HP:0430009" + ], + "small eyelid": [ + "HP:0430009" + ], + "underdevelopment of eyelid": [ + "HP:0430009" + ], + "microblepharia": [ + "HP:0430010" + ], + "abnormally small eyelid": [ + "HP:0430010" + ], + "defect of palpebral conjunctiva": [ + "HP:0430011" + ], + "incomplete ossification of palatine bone": [ + "HP:0430012" + ], + "incomplete calcification of palatine bone": [ + "HP:0430012" + ], + "incomplete formation of palatine bone": [ + "HP:0430012" + ], + "incomplete mineralization of palatine bone": [ + "HP:0430012" + ], + "absent palatine bone ossification": [ + "HP:0430013" + ], + "absence of palatine bone calcification": [ + "HP:0430013" + ], + "absence of palatine bone formation": [ + "HP:0430013" + ], + "absence of palatine bone mineralization": [ + "HP:0430013" + ], + "abnormality of musculature of soft palate": [ + "HP:0430014" + ], + "abnormality of soft palate muscle": [ + "HP:0430014" + ], + "abnormality of soft palate muscles": [ + "HP:0430014" + ], + "abnormal morphology of musculature of pharynx": [ + "HP:0430015" + ], + "abnormality of muscle of the pharynx": [ + "HP:0430015" + ], + "abnormality of muscles of the pharynx": [ + "HP:0430015" + ], + "abnormality of musculature of pharynx": [ + "HP:0430015" + ], + "abnormality of pharyngeal musculature": [ + "HP:0430015" + ], + "abnormality of pharynx musculature": [ + "HP:0430015" + ], + "abnormality of tensor veli palatini muscle": [ + "HP:0430016" + ], + "abnormality of uvular muscle": [ + "HP:0430017" + ], + "abnormality of musculus uvula": [ + "HP:0430017" + ], + "abnormality of musculus uvulae": [ + "HP:0430017" + ], + "abnormality of nasal musculature": [ + "HP:0430018" + ], + "abnormality of muscle of nose": [ + "HP:0430018" + ], 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facial muscle weakness": [ + "HP:0430025" + ], + "bilateral facial paralysis": [ + "HP:0430025" + ], + "paralysis of both side of the face": [ + "HP:0430025" + ], + "paralysis of both sides of the face": [ + "HP:0430025" + ], + "weakness of both side of the face": [ + "HP:0430025" + ], + "weakness of both sides of the face": [ + "HP:0430025" + ], + "abnormality of the shape of the midface": [ + "HP:0430026" + ], + "abnormal morphology of the midface": [ + "HP:0430026" + ], + "dysmorphic midface": [ + "HP:0430026" + ], + "hyperplasia of the maxilla": [ + "HP:0430028" + ], + "big maxilla": [ + "HP:0430028" + ], + "big upper jaw": [ + "HP:0430028" + ], + "hyperplasia of upper jaw": [ + "HP:0430028" + ], + "hypertrophy of maxilla": [ + "HP:0430028" + ], + "hypertrophy of upper jaw": [ + "HP:0430028" + ], + "increase projection of maxilla": [ + "HP:0430028" + ], + "increased projection of maxilla": [ + "HP:0430028" + ], + "increase projection of upper jaw": [ + "HP:0430028" + ], + 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proportion of immature gamma - delta t lymphocytes": [ + "HP:0500272" + ], + "abnormal proportion of immature gamma - delta t - cell": [ + "HP:0500272" + ], + "abnormal proportion of immature gamma - delta t - cells": [ + "HP:0500272" + ], + "abnormal proportion of immature gamma - delta t - lymphocyte": [ + "HP:0500272" + ], + "abnormal proportion of immature gamma - delta t - lymphocytes": [ + "HP:0500272" + ], + "increase proportion of immature gamma - delta t cell": [ + "HP:0500273" + ], + "increased proportion of immature gamma - delta t cells": [ + "HP:0500273" + ], + "elevate proportion of immature gamma - delta t cell": [ + "HP:0500273" + ], + "elevated proportion of immature gamma - delta t cells": [ + "HP:0500273" + ], + "increase proportion of immature gamma - delat t lymphocyte": [ + "HP:0500273" + ], + "increased proportion of immature gamma - delat t lymphocytes": [ + "HP:0500273" + ], + "increase proportion of immature gamma - delta t - cell": [ + "HP:0500273" + ], + "increased proportion of immature gamma - delta t - cells": [ + "HP:0500273" + ], + "increase proportion of immature gamma - delta t - lymphocyte": [ + "HP:0500273" + ], + "increased proportion of immature gamma - delta t - lymphocytes": [ + "HP:0500273" + ], + "decreased proportion of immature gamma - delta t cell": [ + "HP:0500274" + ], + "decreased proportion of immature gamma - delta t cells": [ + "HP:0500274" + ], + "decreased proportion of immature gamma - delta t lymphocyte": [ + "HP:0500274" + ], + "decreased proportion of immature gamma - delta t lymphocytes": [ + "HP:0500274" + ], + "decreased proportion of immature gamma - delta t - cell": [ + "HP:0500274" + ], + "decreased proportion of immature gamma - delta t - cells": [ + "HP:0500274" + ], + "decreased proportion of immature gamma - delta t - lymphocyte": [ + "HP:0500274" + ], + "decreased proportion of immature gamma - delta t - lymphocytes": [ + "HP:0500274" + ], + "reduce proportion of immature gamma - delta t cell": 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"abnormality of cartilage of external ear": [ + "HP:3000022" + ], + "abnormality of angular artery": [ + "HP:3000023" + ], + "abnormal facial artery morphology": [ + "HP:3000024" + ], + "abnormality of facial artery": [ + "HP:3000024" + ], + "abnormality of ciliary ganglion": [ + "HP:3000025" + ], + "obsolete abnormality of common carotid artery plus branch": [ + "HP:3000026" + ], + "obsolete abnormality of common carotid artery plus branches": [ + "HP:3000026" + ], + "abnormality of buccinator muscle": [ + "HP:3000027" + ], + "abnormality of depressor anguli oris muscle": [ + "HP:3000028" + ], + "abnormality of depressor labii inferioris": [ + "HP:3000029" + ], + "abnormality of depressor labii inferioris muscle": [ + "HP:3000029" + ], + "abnormality of bony orbit of skull": [ + "HP:3000030" + ], + "abnormality of bone of the orbit of the skull": [ + "HP:3000030" + ], + "abnormality of bones of the orbit of the skull": [ + "HP:3000030" + ], + "abnormality of the bony eye socket": [ + 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"anti - ak5 antibody positivity": [ + "HP:5000000" + ], + "anti - ampar antibody positivity": [ + "HP:5000001" + ], + "anti - alpha - amino - 3 - hydroxy - 5 - methyl - 4 - isoxazolepropionic acid receptor antibody": [ + "HP:5000001" + ], + "anti - amphiphysin antibody": [ + "HP:5000002" + ], + "anti - arhgap26 antibody": [ + "HP:5000003" + ], + "anti - ca antibody": [ + "HP:5000003" + ], + "anti - rhogtpase - activate protein 26 antibody": [ + "HP:5000003" + ], + "anti - rhogtpase - activating protein 26 antibody": [ + "HP:5000003" + ], + "anti - carp viii antibody": [ + "HP:5000004" + ], + "anti carpviii antibody": [ + "HP:5000004" + ], + "anti - carbonic anhydrase - related protein viii antibody": [ + "HP:5000004" + ], + "anti - caspr2": [ + "HP:5000005" + ], + "anti - caspr2 antibody": [ + "HP:5000005" + ], + "anti - contactin - associate protein - like 2 antibody": [ + "HP:5000005" + ], + "anti - contactin - associated protein - like 2 antibody": [ + "HP:5000005" + ], + "anti - cv2 / crmp5 antibody": [ + "HP:5000006" + ], + "anti - cv2 antibody": [ + "HP:5000006" + ], + "anti - cv2 / collapsin response mediator protein ( crmp ) 5 antibody": [ + "HP:5000006" + ], + "anti - dppx antibody": [ + "HP:5000007" + ], + "anti - dipeptidyl - peptidase - like protein 6 antibody": [ + "HP:5000007" + ], + "anti - fgfr3 antibody": [ + "HP:5000008" + ], + "anti - fibroblast growth factor receptor 3 antibody": [ + "HP:5000008" + ], + "anti - gaba ( a ) r antibody": [ + "HP:5000009" + ], + "anti - gabaa r antibody": [ + "HP:5000009" + ], + "anti - gamma amino butyric acid type a receptor antibody": [ + "HP:5000009" + ], + "anti - gamma amino butyric acid type a receptors antibody": [ + "HP:5000009" + ], + "anti - gaba ( b ) r antibody": [ + "HP:5000010" + ], + "anti - gamma - aminobutyric acid b receptor antibody": [ + "HP:5000010" + ], + "anti - gad65 antibody": [ + "HP:5000011" + ], + "anti - glutamic acid decarboxylase 65 antibody": [ + "HP:5000011" + ], + "anti - gephyrin antibody": [ + "HP:5000012" + ], + "anti - gfap antibody": [ + "HP:5000013" + ], + "anti - glial fibrillary acidic protein antibody": [ + "HP:5000013" + ], + "anti - glyr antibody": [ + "HP:5000014" + ], + "anti - glycine receptor antibody": [ + "HP:5000014" + ], + "anti - homer - 3 antibody": [ + "HP:5000015" + ], + "anti - homer protein homolog 3 antibody": [ + "HP:5000015" + ], + "anti - hu antibody": [ + "HP:5000016" + ], + "anti - anna - 1 antibody": [ + "HP:5000016" + ], + "anti - neuronal nuclear antibody type - 1 antibody": [ + "HP:5000016" + ], + "anti - iglon5 antibody": [ + "HP:5000017" + ], + "anti - immunoglobulin - like cell adhesion molecule 5 antibody": [ + "HP:5000017" + ], + "anti - itpr1 antibody": [ + "HP:5000018" + ], + "anti - inositol 1,4,5 - trisphosphate receptor type 1 antibody": [ + "HP:5000018" + ], + "anti - klhl11 antibody": [ + "HP:5000019" + ], + "anti - kelch - like protein 11 antibody": [ + "HP:5000019" + ], + "anti - lgi1 antibody": [ + "HP:5000020" + ], + "anti - anti - leucine - rich glioma - inactivated 1 antibody": [ + "HP:5000020" + ], + "anti - ma antibody": [ + "HP:5000021" + ], + "anti - ma2 antibody": [ + "HP:5000022" + ], + "anti - ta antibody": [ + "HP:5000022" + ], + "anti - ma1 antibody": [ + "HP:5000023" + ], + "anti - mglur1 antibody": [ + "HP:5000024" + ], + "anti - metabotropic glutamate receptor 1 antibody": [ + "HP:5000024" + ], + "anti - mglur5 antibody": [ + "HP:5000025" + ], + "anti - metabotropic glutamate receptor type 5 antibody": [ + "HP:5000025" + ], + "anti - neurexin - 3alpha antibody": [ + "HP:5000026" + ], + "anti - p / q - type vgcc antibody": [ + "HP:5000027" + ], + "anti - p / q - type voltage - gated calcium - channel antibody": [ + "HP:5000027" + ], + "anti - map1b antibody": [ + "HP:5000028" + ], + "anti - microtubule - associate protein 1b antibody": [ + "HP:5000028" + ], + "anti - microtubule - associated protein 1b antibody": [ + "HP:5000028" + ], + "anti - purkinje cell cytoplasmic type - 2 antibody": [ + "HP:5000028" + ], + "anti - pkcgamma antibody": [ + "HP:5000029" + ], + "anti - protein kinase c gamma antibody": [ + "HP:5000029" + ], + "anti - ri antibody": [ + "HP:5000030" + ], + "anti - anna - 2 antibody": [ + "HP:5000030" + ], + "anti - septin - 5 antibody": [ + "HP:5000031" + ], + "anti - sez6l2 antibody": [ + "HP:5000032" + ], + "anti - sox1 antibody": [ + "HP:5000033" + ], + "anti - sry - like high mobility group box ( sox ) 1 antibody": [ + "HP:5000033" + ], + "anti - tr / dner antibody": [ + "HP:5000034" + ], + "anti - delta / notch - like epidermal growth factor - related receptor antibody": [ + "HP:5000034" + ], + "pca - tr": [ + "HP:5000034" + ], + "anti - trim46 antibody": [ + "HP:5000035" + ], + "anti - trim9 / trim67 antibody": [ + "HP:5000036" + ], + "anti - yo antibody": [ + "HP:5000037" + ], + "anti - purkinje cell cytoplasmic antibody 1": [ + "HP:5000037" + ], + "anti - titin antibody": [ + "HP:5000038" + ], + "anti - zic4 antibody": [ + "HP:5000039" + ], + "anti - crmp5 antibody": [ + "HP:5000041" + ], + "anti - collapsin response - mediate protein 5 antibody": [ + "HP:5000041" + ], + "anti - collapsin response - mediated protein 5 antibody": [ + "HP:5000041" + ], + "anti - sj / itpr1 antibody": [ + "HP:5000042" + ], + "anti - sj / inositol 1,4,5 - trisphosphate receptor antibody": [ + "HP:5000042" + ], + "anti - d2 r antibody": [ + "HP:5000043" + ], + "anti - dopamine - 2 receptor ( d2r ) antibody": [ + "HP:5000043" + ], + "anti - dopamine - 2 receptors ( d2r ) antibody": [ + "HP:5000043" + ], + "anti - gluk2 antibody": [ + "HP:5000044" + ], + "anti - glutamate kainate receptor subunit 2 antibody": [ + "HP:5000044" + ], + "anti - anti - muscle - specific tyrosine kinase antibody": [ + "HP:5000045" + ], + "anti - lrp4 antibody": [ + "HP:5000046" + ], + "anti - low - density lipoprotein receptor - related protein 4 antibody": [ + "HP:5000046" + ], + "anti - ryanodine receptor antibody": [ + "HP:5000047" + ], + "anti - ryr antibody": [ + "HP:5000047" + ], + "anti - kv1.4 antibody": [ + "HP:5000048" + ] +} \ No newline at end of file