|
OMIM |
Link |
Information gain |
01 |
|
dubowitz syndrome
|
[NCBI]
|
0.00635605
|
|
|
dermatitis, atopic
|
[NCBI]
|
0.00130285
|
|
|
NCR
|
[NCBI]
|
0.000737684
|
|
|
actinic prurigo
|
[NCBI]
|
0.000587372
|
|
|
WAS
|
[NCBI]
|
0.000558847
|
|
|
spondyloepimetaphyseal dysplasia, sponastrime type
|
[NCBI]
|
0.000545541
|
|
|
hyperimmunoglobulin e recurrent infection syndrome, autosomal dominant
|
[NCBI]
|
0.000246119
|
|
|
growth retardation, small and puffy hands and feet, and eczema
|
[NCBI]
|
0.000132242
|
|
|
immunodeficiency with defective leukocyte and lymphocyte function and with response to histamine-1 antagonist
|
[NCBI]
|
9.57923e-05
|
|
|
lymphoma, non-hodgkin, familial
|
[NCBI]
|
8.24252e-05
|
|
|
complement component 5 deficiency
|
[NCBI]
|
7.79657e-05
|
|
|
kindler syndrome
|
[NCBI]
|
7.64945e-05
|
|
|
NETH
|
[NCBI]
|
6.97129e-05
|
|
|
IPEX
|
[NCBI]
|
6.7161e-05
|
|
|
CCL27
|
[NCBI]
|
6.48204e-05
|
|
|
IGER
|
[NCBI]
|
5.78811e-05
|
|
|
ED1
|
[NCBI]
|
5.17599e-05
|
|
|
RNASE3
|
[NCBI]
|
5.07586e-05
|
|
|
HMI
|
[NCBI]
|
4.69181e-05
|
|
|
FOXP3
|
[NCBI]
|
4.62854e-05
|
|
|
WAS
|
[NCBI]
|
4.58851e-05
|
|
|
CCL17
|
[NCBI]
|
4.36168e-05
|
|
|
FGFR2
|
[NCBI]
|
3.62047e-05
|
|
|
PXE
|
[NCBI]
|
2.89563e-05
|
|
|
PF4
|
[NCBI]
|
2.6804e-05
|
|
|
TNFSF6
|
[NCBI]
|
1.77374e-05
|
|
|
VIP
|
[NCBI]
|
1.73372e-05
|
|
|
RA
|
[NCBI]
|
1.23195e-05
|
|
|
MPO
|
[NCBI]
|
9.62258e-06
|
|
|
NGFB
|
[NCBI]
|
9.48694e-06
|
|
|
CEACAM5
|
[NCBI]
|
5.06577e-06
|
|