|
OMIM |
Link |
Information gain |
01 |
|
WS1
|
[NCBI]
|
0.00571134
|
|
|
microphthalmia with limb anomalies
|
[NCBI]
|
0.0034825
|
|
|
WS2B
|
[NCBI]
|
0.003153
|
|
|
PAX3
|
[NCBI]
|
0.00298892
|
|
|
ADFN
|
[NCBI]
|
0.00214098
|
|
|
MITF
|
[NCBI]
|
0.00137362
|
|
|
WS2A
|
[NCBI]
|
0.00126209
|
|
|
waardenburg-shah syndrome
|
[NCBI]
|
0.00104624
|
|
|
waardenburg syndrome, type iic
|
[NCBI]
|
0.0010375
|
|
|
WS3
|
[NCBI]
|
0.000904373
|
|
|
deafness, congenital, with vitiligo and achalasia
|
[NCBI]
|
0.000819746
|
|
|
SOX10
|
[NCBI]
|
0.000570429
|
|
|
acrodysostosis
|
[NCBI]
|
0.000545541
|
|
|
EDN3
|
[NCBI]
|
0.00045542
|
|
|
tietz syndrome
|
[NCBI]
|
0.000408107
|
|
|
albinism, ocular, with sensorineural deafness
|
[NCBI]
|
0.00033621
|
|
|
PCWH
|
[NCBI]
|
0.000299763
|
|
|
HSCR1
|
[NCBI]
|
0.000276739
|
|
|
CDHS
|
[NCBI]
|
0.000179044
|
|
|
EDNRB
|
[NCBI]
|
0.000176727
|
|
|
ALPI
|
[NCBI]
|
0.000146616
|
|
|
WS2E
|
[NCBI]
|
0.000111888
|
|
|
waardenburg syndrome, type iid
|
[NCBI]
|
8.94311e-05
|
|
|
abcd syndrome
|
[NCBI]
|
8.09651e-05
|
|
|
TYR
|
[NCBI]
|
5.73282e-05
|
|
|
PBT
|
[NCBI]
|
5.49323e-05
|
|
|
PAX4
|
[NCBI]
|
5.42838e-05
|
|
|
PAX7
|
[NCBI]
|
5.42838e-05
|
|
|
UBE2I
|
[NCBI]
|
5.42838e-05
|
|
|
HPS
|
[NCBI]
|
5.33556e-05
|
|
|
SNAI2
|
[NCBI]
|
5.09122e-05
|
|
|
CHRND
|
[NCBI]
|
4.84067e-05
|
|
|
crouzon syndrome
|
[NCBI]
|
4.78347e-05
|
|
|
CHS
|
[NCBI]
|
4.54257e-05
|
|
|
dyschromatosis symmetrica hereditaria 1
|
[NCBI]
|
4.23908e-05
|
|
|
PAX1
|
[NCBI]
|
4.20947e-05
|
|
|
PAX9
|
[NCBI]
|
4.09941e-05
|
|
|
PAX5
|
[NCBI]
|
3.91059e-05
|
|
|
ODDD
|
[NCBI]
|
3.8381e-05
|
|
|
PAX8
|
[NCBI]
|
3.68192e-05
|
|
|
OCA1A
|
[NCBI]
|
3.55769e-05
|
|
|
FN1
|
[NCBI]
|
3.49679e-05
|
|
|
TCOF1
|
[NCBI]
|
3.29461e-05
|
|
|
PAX2
|
[NCBI]
|
3.25003e-05
|
|
|
TCOF
|
[NCBI]
|
2.87088e-05
|
|
|
HGPS
|
[NCBI]
|
2.67972e-05
|
|
|
ASS
|
[NCBI]
|
2.15815e-05
|
|
|
GDNF
|
[NCBI]
|
1.95156e-05
|
|
|
BCNS
|
[NCBI]
|
1.51349e-05
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
1.10086e-05
|
|
|
HD
|
[NCBI]
|
2.94552e-06
|
|