update causal gene discovery patients

gene_discovery_scores_attn.csv

@@ -8,7 +8,7 @@ UDN-P2,Abnormality of coordination,9,0.0462948195636272
 UDN-P2,Developmental regression,203,0.0459261648356914
 UDN-P2,Delayed speech and language development,512,0.0430936887860298
 UDN-P2,Narrow forehead,10,0.0407348088920116
-UDN-P2,HP:0007930,502,0.0347550734877586
+UDN-P2,Prominent epicanthal folds,502,0.0347550734877586
 UDN-P2,Tapered finger,1,0.0334602817893028
 UDN-P2,Astigmatism,135,0.0263907611370086
 UDN-P2,Esotropia,121,0.0251658950001001
@@ -18,8 +18,8 @@ UDN-P2,Apraxia,47,0.0208667255938053
 UDN-P2,Obesity,444,0.0207838024944067
 UDN-P2,Brachydactyly,389,0.019670233130455
 UDN-P2,Hypotelorism,2,0.019594058394432
-UDN-P2,HP:0011398,911,0.0195294171571731
-UDN-P2,HP:0006877,1425,0.0191374626010656
+UDN-P2,Central hypotonia,911,0.0195294171571731
+UDN-P2,Mental retardation,1425,0.0191374626010656
 UDN-P2,Incoordination,62,0.0164797715842723
 UDN-P2,Poor coordination,31,0.0149749955162405
 UDN-P2,Speech apraxia,1,0.0129641536623239
@@ -60,13 +60,13 @@ UDN-P1,Short stature,1167,0.0120520433411002
 UDN-P1,Constipation,270,0.0114372400566935
 UDN-P1,Failure to thrive,648,0.0112343775108456
 UDN-P1,Growth delay,435,0.0110889645293354
-UDN-P1,HP:0040199,1,0.0105574298650026
+UDN-P1,Midface retrusion,1,0.0105574298650026
 UDN-P1,Hydrocephalus,304,0.0098500475287437
 UDN-P1,Alacrima,1,0.0098224878311157
 UDN-P1,Chronic pancreatitis,1,0.007521613035351
-UDN-P1,HP:0008033,94,0.0067969802767038
+UDN-P1,Exotropia,94,0.0067969802767038
 UDN-P1,Global developmental delay,1330,0.0066903717815876
-UDN-P1,HP:0011398,911,0.0062526292167603
+UDN-P1,Hypotonia,911,0.0062526292167603
 UDN-P1,Overlapping toe,2,0.0060891341418027
 UDN-P1,Drooling,85,0.0057123596780002
 UDN-P1,Gastroesophageal reflux,268,0.005148937460035