|
OMIM |
Link |
Information
gain |
01 |
|
|
candidiasis, familial chronic mucocutaneous, autosomal dominant
|
[NCBI]
|
0.00297661
|
|
|
|
candidiasis, familial chronic mucocutaneous, autosomal dominant, with thyroid disease
|
[NCBI]
|
0.000898321
|
|
|
|
candidiasis, familial chronic mucocutaneous, autosomal recessive
|
[NCBI]
|
0.000844965
|
|
|
|
APS2
|
[NCBI]
|
0.000657993
|
|
|
|
APS1
|
[NCBI]
|
0.000330086
|
|
|
|
lymphokine deficiency
|
[NCBI]
|
0.000148254
|
|
|
|
lymphoblastic transformation, intrinsic defect in
|
[NCBI]
|
0.000148254
|
|
|
|
lymphoblastic transformation, inhibition of
|
[NCBI]
|
0.000148254
|
|
|
|
monocyte chemotactic disorder
|
[NCBI]
|
0.000148254
|
|
|
|
immunodeficiency with defective leukocyte and lymphocyte function and with response to histamine-1 antagonist
|
[NCBI]
|
0.000111796
|
|
|
|
autoimmune disease
|
[NCBI]
|
8.66284e-05
|
|
|
|
AEZ
|
[NCBI]
|
7.95849e-05
|
|
|
|
hyperimmunoglobulin e recurrent infection syndrome, autosomal dominant
|
[NCBI]
|
7.89629e-05
|
|
|
|
hla-d histocompatibility type
|
[NCBI]
|
4.59243e-05
|
|
|
|
SOD2
|
[NCBI]
|
4.0261e-05
|
|
|
|
APOE
|
[NCBI]
|
2.41217e-05
|
|
