|
OMIM |
Link |
Information
gain |
01 |
|
|
immunodeficiency with cleft lip/palate, cataract, hypopigmentation, and absent corpus callosum
|
[NCBI]
|
0.000991404
|
|
|
|
NCR
|
[NCBI]
|
0.000991404
|
|
|
|
hyperimmunoglobulin e-recurrent infection syndrome, autosomal recessive
|
[NCBI]
|
0.000991404
|
|
|
|
EV
|
[NCBI]
|
0.000267683
|
|
|
|
lymphoblastic transformation, intrinsic defect in
|
[NCBI]
|
0.000140314
|
|
|
|
granulomatous disease with defect in neutrophil chemotaxis
|
[NCBI]
|
0.000117844
|
|
|
|
immunodeficiency with defective leukocyte and lymphocyte function and with response to histamine-1 antagonist
|
[NCBI]
|
0.000103859
|
|
|
|
tuftsin deficiency
|
[NCBI]
|
9.97657e-05
|
|
|
|
ichthyosis vulgaris
|
[NCBI]
|
8.07952e-05
|
|
|
|
keratitis-ichthyosis-deafness syndrome, autosomal dominant
|
[NCBI]
|
7.77539e-05
|
|
|
|
SCN1
|
[NCBI]
|
7.60048e-05
|
|
|
|
hyperimmunoglobulin e recurrent infection syndrome, autosomal dominant
|
[NCBI]
|
7.10508e-05
|
|
|
|
DCD
|
[NCBI]
|
7.10164e-05
|
|
|
|
LAD
|
[NCBI]
|
6.82623e-05
|
|
|
|
CHH
|
[NCBI]
|
5.50831e-05
|
|
|
|
ITGB2
|
[NCBI]
|
5.35982e-05
|
|
|
|
MPO
|
[NCBI]
|
4.19008e-05
|
|
|
|
MBL2
|
[NCBI]
|
3.52488e-05
|
|
|
|
PF4
|
[NCBI]
|
3.14811e-05
|
|
|
|
HGF
|
[NCBI]
|
1.7369e-05
|
|
|
|
RA
|
[NCBI]
|
1.1009e-05
|
|
|
|
SLE
|
[NCBI]
|
4.85239e-06
|
|
