|
OMIM |
Link |
Information
gain |
01 |
|
|
IGAD1
|
[NCBI]
|
0.00493359
|
|
|
|
ocular motor apraxia
|
[NCBI]
|
0.000625244
|
|
|
|
pulmonary alveolar proteinosis, acquired
|
[NCBI]
|
0.000588308
|
|
|
|
dubowitz syndrome
|
[NCBI]
|
0.000447771
|
|
|
|
HIGM1
|
[NCBI]
|
0.000307185
|
|
|
|
CVID
|
[NCBI]
|
0.000286387
|
|
|
|
epilepsy-telangiectasia
|
[NCBI]
|
0.000127818
|
|
|
|
secretory component deficiency
|
[NCBI]
|
0.000127818
|
|
|
|
IGKC
|
[NCBI]
|
0.00012265
|
|
|
|
AT
|
[NCBI]
|
0.00010979
|
|
|
|
SH2D1A
|
[NCBI]
|
0.000103474
|
|
|
|
IGHG2
|
[NCBI]
|
7.77884e-05
|
|
|
|
vitiligo
|
[NCBI]
|
7.69732e-05
|
|
|
|
IGHG3
|
[NCBI]
|
7.25879e-05
|
|
|
|
IGHA1
|
[NCBI]
|
7.25879e-05
|
|
|
|
IGLC1
|
[NCBI]
|
6.67002e-05
|
|
|
|
mulibrey nanism
|
[NCBI]
|
6.53139e-05
|
|
|
|
BCGF
|
[NCBI]
|
5.63852e-05
|
|
|
|
immunodeficiency-centromeric instability-facial anomalies syndrome
|
[NCBI]
|
5.48822e-05
|
|
|
|
XLP1
|
[NCBI]
|
5.30777e-05
|
|
|
|
IGHG1
|
[NCBI]
|
4.98541e-05
|
|
|
|
C3
|
[NCBI]
|
4.64608e-05
|
|
|
|
A2M
|
[NCBI]
|
4.43952e-05
|
|
|
|
BLM
|
[NCBI]
|
4.19619e-05
|
|
|
|
MAG
|
[NCBI]
|
2.8933e-05
|
|
|
|
PI
|
[NCBI]
|
2.63966e-05
|
|
|
|
WAS
|
[NCBI]
|
2.06881e-05
|
|
|
|
TTR
|
[NCBI]
|
1.89232e-05
|
|
|
|
RA
|
[NCBI]
|
1.15457e-05
|
|
|
|
CD
|
[NCBI]
|
1.01337e-05
|
|
|
|
CF
|
[NCBI]
|
9.30535e-06
|
|
|
|
lymphoma, non-hodgkin, familial
|
[NCBI]
|
8.22473e-06
|
|
|
|
SLE
|
[NCBI]
|
7.33661e-06
|
|
|
|
AFP
|
[NCBI]
|
6.79479e-06
|
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
3.82723e-06
|
|
|
|
CEACAM5
|
[NCBI]
|
2.98286e-06
|
|
