|
OMIM |
Link |
Information gain |
01 |
|
HFM
|
[NCBI]
|
0.000970108
|
|
|
femur, unilateral bifid, with monodactylous ectrodactyly
|
[NCBI]
|
0.000773718
|
|
|
ASD1
|
[NCBI]
|
0.00074746
|
|
|
tracheoesophageal fistula with or without esophageal atresia
|
[NCBI]
|
0.000735185
|
|
|
SHFLD1
|
[NCBI]
|
0.000657993
|
|
|
hypertelorism with esophageal abnormality and hypospadias
|
[NCBI]
|
0.000424981
|
|
|
feingold syndrome
|
[NCBI]
|
0.000394765
|
|
|
vater association
|
[NCBI]
|
0.000296274
|
|
|
gastrointestinal abnormalities, multiple
|
[NCBI]
|
0.000235506
|
|
|
SHH
|
[NCBI]
|
0.000187337
|
|
|
microcephaly and digital abnormalities with normal intelligence
|
[NCBI]
|
0.000110422
|
|
|
cleft larynx, posterior
|
[NCBI]
|
8.90891e-05
|
|
|
vacterl association with hydrocephalus
|
[NCBI]
|
8.40597e-05
|
|
|
ITGA6
|
[NCBI]
|
7.91457e-05
|
|
|
MCOPS3
|
[NCBI]
|
7.13081e-05
|
|
|
FMD
|
[NCBI]
|
7.03584e-05
|
|
|
ITGB4
|
[NCBI]
|
6.23221e-05
|
|
|
MKKS
|
[NCBI]
|
6.14083e-05
|
|
|
charge syndrome
|
[NCBI]
|
5.80894e-05
|
|
|
FA
|
[NCBI]
|
5.28522e-05
|
|
|
RTS
|
[NCBI]
|
5.18126e-05
|
|
|
MTTL1
|
[NCBI]
|
4.46023e-05
|
|
|
DGS
|
[NCBI]
|
3.31565e-05
|
|
|
GDNF
|
[NCBI]
|
2.63337e-05
|
|
|
VIP
|
[NCBI]
|
2.04899e-05
|
|
|
SLE
|
[NCBI]
|
1.61237e-05
|
|