|
OMIM |
Link |
Information
gain |
01 |
|
|
trichoepithelioma, multiple familial
|
[NCBI]
|
0.000833714
|
|
|
|
acetabular dysplasia
|
[NCBI]
|
0.000801832
|
|
|
|
hodgkin disease, x-linked pseudoautosomal
|
[NCBI]
|
0.000801832
|
|
|
|
OTSC1
|
[NCBI]
|
0.000710576
|
|
|
|
OFC1
|
[NCBI]
|
0.000409023
|
|
|
|
autism
|
[NCBI]
|
0.000380133
|
|
|
|
hemochromatosis, neonatal
|
[NCBI]
|
0.000223007
|
|
|
|
IHPS1
|
[NCBI]
|
0.000198634
|
|
|
|
IS1
|
[NCBI]
|
0.000198095
|
|
|
|
HMS1
|
[NCBI]
|
0.000188977
|
|
|
|
TD1
|
[NCBI]
|
0.000130402
|
|
|
|
LNPEP
|
[NCBI]
|
9.95021e-05
|
|
|
|
corticosterone methyloxidase type i deficiency
|
[NCBI]
|
9.90237e-05
|
|
|
|
kawasaki disease
|
[NCBI]
|
8.6096e-05
|
|
|
|
CPI
|
[NCBI]
|
8.5861e-05
|
|
|
|
tetralogy of fallot
|
[NCBI]
|
8.10864e-05
|
|
|
|
cri-du-chat syndrome
|
[NCBI]
|
8.10864e-05
|
|
|
|
hodgkin lymphoma
|
[NCBI]
|
7.09344e-05
|
|
|
|
EFE
|
[NCBI]
|
7.00725e-05
|
|
|
|
neural tube defects
|
[NCBI]
|
6.69608e-05
|
|
|
|
apert syndrome
|
[NCBI]
|
6.62546e-05
|
|
|
|
LGMD2C
|
[NCBI]
|
6.49146e-05
|
|
|
|
FOP
|
[NCBI]
|
5.9819e-05
|
|
|
|
osteogenesis imperfecta, type iia
|
[NCBI]
|
5.66165e-05
|
|
|
|
RA
|
[NCBI]
|
5.55631e-05
|
|
|
|
HD
|
[NCBI]
|
4.4013e-05
|
|
|
|
VHL
|
[NCBI]
|
4.18777e-05
|
|
|
|
lymphoma, non-hodgkin, familial
|
[NCBI]
|
4.18245e-05
|
|
|
|
SCZD
|
[NCBI]
|
4.16868e-05
|
|
|
|
FRDA
|
[NCBI]
|
4.09428e-05
|
|
|
|
ACH
|
[NCBI]
|
3.98811e-05
|
|
|
|
JARID1D
|
[NCBI]
|
3.95298e-05
|
|
|
|
CYP11B2
|
[NCBI]
|
3.53128e-05
|
|
|
|
RTT
|
[NCBI]
|
2.54594e-05
|
|
|
|
hemophilia a
|
[NCBI]
|
2.51861e-05
|
|
|
|
NF1
|
[NCBI]
|
2.25607e-05
|
|
|
|
GTS
|
[NCBI]
|
2.10249e-05
|
|
|
|
TS
|
[NCBI]
|
1.61267e-05
|
|
|
|
CD
|
[NCBI]
|
1.18916e-05
|
|
|
|
FA
|
[NCBI]
|
1.1574e-05
|
|
|
|
CF
|
[NCBI]
|
2.36594e-06
|
|
|
|
AD
|
[NCBI]
|
7.39775e-09
|
|
