patient_id,candidate_patients,similarities,correct_label,genes,diseases,disease_ids
UDN-P4,SIM-P7513,0.0001346864301012,0.0,REEP1,Autosomal dominant spastic paraplegia type 31,101011
UDN-P4,SIM-P38172,0.0001341508032055,0.0,KIF1A,Autosomal spastic paraplegia type 30,101010
UDN-P4,SIM-P31298,0.0001340870658168,0.0,DDHD1,Autosomal recessive spastic paraplegia type 28,101008
UDN-P4,SIM-P19068,0.0001340282615274,1.0,CAPN1,Autosomal recessive spastic paraplegia type 76,488594
UDN-P4,SIM-P19513,0.0001340070302831,0.0,ATL1,Autosomal dominant spastic paraplegia type 3,100984
UDN-P4,SIM-P36075,0.000133997775265,0.0,MTPAP,Autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome,254343
UDN-P4,SIM-P18901,0.000133881723741,0.0,TDP1,Spinocerebellar ataxia with axonal neuropathy type 1,94124
UDN-P4,SIM-P20117,0.000133869878482,0.0,SPAST,Autosomal dominant spastic paraplegia type 4,100985
UDN-P4,SIM-P41708,0.0001337969733867,0.0,SPG19,Autosomal dominant spastic paraplegia type 19,100999
UDN-P4,SIM-P24993,0.0001337462454102,0.0,SPG19,Autosomal dominant spastic paraplegia type 19,100999
UDN-P6,SIM-P34720,0.0001335124979959,0.0,PMM2,PMM2-CDG,79318
UDN-P6,SIM-P6961,0.000133484849357,0.0,AP1S2,X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome,85329
UDN-P6,SIM-P39957,0.0001328073558397,0.0,TCF4,Pitt-Hopkins syndrome,2896
UDN-P6,SIM-P13143,0.0001326532074017,0.0,SSR4,SSR4-CDG,370927
UDN-P6,SIM-P21183,0.0001325271441601,0.0,KAT6A,Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome,457193
UDN-P6,SIM-P27029,0.0001323336182394,0.0,ATRX,Chudley-Lowry-Hoar syndrome,93971
UDN-P6,SIM-P26917,0.0001322419411735,0.0,NONO,Macrocephaly-intellectual disability-left ventricular non compaction syndrome,466791
UDN-P6,SIM-P13788,0.0001321789313806,0.0,NRXN1,Pitt-Hopkins-like syndrome,221150
UDN-P6,SIM-P3592,0.0001321435265708,0.0,FRMD4A,Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome,466688
UDN-P6,SIM-P24214,0.0001321362215094,0.0,AP1S2,X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome,85329
UDN-P5,SIM-P12152,0.0001249182969331,0.0,MYD88,Waldenström macroglobulinemia,33226
UDN-P5,SIM-P23023,0.0001241921563632,0.0,TNFRSF1A,Tumor necrosis factor receptor 1 associated periodic syndrome,32960
UDN-P5,SIM-P30461,0.0001231428614119,0.0,MYD88,Waldenström macroglobulinemia,33226
UDN-P5,SIM-P6717,0.0001229638874065,0.0,MYD88,Waldenström macroglobulinemia,33226
UDN-P5,SIM-P30356,0.00012291384337,0.0,PSTPIP1,Pyogenic arthritis-pyoderma gangrenosum-acne syndrome,69126
UDN-P5,SIM-P35189,0.0001224889274453,0.0,NLRC4,Familial cold urticaria,47045
UDN-P5,SIM-P20277,0.0001221649872604,0.0,CPOX,Hereditary coproporphyria,79273
UDN-P5,SIM-P7603,0.000121750497783,0.0,NLRP3,Familial cold urticaria,47045
UDN-P5,SIM-P8138,0.0001210815316881,0.0,MEFV,Familial Mediterranean fever,342
UDN-P5,SIM-P36107,0.0001210761329275,0.0,TNFRSF1A,Tumor necrosis factor receptor 1 associated periodic syndrome,32960
UDN-P3,SIM-P17696,0.0001152271579485,0.0,GRIA3,X-linked intellectual disability due to GRIA3 mutations,364028
UDN-P3,SIM-P12018,0.0001116794228437,1.0,RPS6KA3,Symptomatic form of Coffin-Lowry syndrome in female carriers,276630
UDN-P3,SIM-P13072,0.0001079059220501,0.0,THOC2,X-linked intellectual disability-short stature-overweight syndrome,457240
UDN-P3,SIM-P27682,0.0001075164036592,0.0,AP1S2,Fried syndrome,85335
UDN-P3,SIM-P17495,0.0001061590883182,0.0,SMS,"X-linked intellectual disability, Snyder type",3063
UDN-P3,SIM-P12040,0.000106000341475,0.0,AP1S2,Fried syndrome,85335
UDN-P3,SIM-P38032,0.0001052861043717,0.0,UBE3A,Angelman syndrome due to a point mutation,411511
UDN-P3,SIM-P15144,0.0001048136182362,0.0,PHF8,"X-linked intellectual disability, Siderius type",85287
UDN-P3,SIM-P2560,0.0001046940378728,0.0,AP1S2,Fried syndrome,85335
UDN-P3,SIM-P13027,0.000104646103864,0.0,FMR1,Fragile X syndrome,908