|
OMIM |
Link |
Information gain |
01 |
|
candidiasis, familial chronic mucocutaneous, autosomal recessive
|
[NCBI]
|
0.00102023
|
|
|
APS1
|
[NCBI]
|
0.000941372
|
|
|
hemophagocytic lymphohistiocytosis, familial, 1
|
[NCBI]
|
0.000624176
|
|
|
myeloperoxidase deficiency
|
[NCBI]
|
0.000286468
|
|
|
MPO
|
[NCBI]
|
0.000216629
|
|
|
TNF
|
[NCBI]
|
0.000196595
|
|
|
CLEC7A
|
[NCBI]
|
0.000138014
|
|
|
CHS
|
[NCBI]
|
0.00012781
|
|
|
secretory component deficiency
|
[NCBI]
|
0.000125989
|
|
|
lymphoid system deterioration, progressive
|
[NCBI]
|
0.000125989
|
|
|
CTSG
|
[NCBI]
|
0.00011538
|
|
|
lazy leukocyte syndrome
|
[NCBI]
|
8.95465e-05
|
|
|
GCA
|
[NCBI]
|
7.84043e-05
|
|
|
GAPDH
|
[NCBI]
|
6.71576e-05
|
|
|
kaposi sarcoma
|
[NCBI]
|
6.65269e-05
|
|
|
PI6
|
[NCBI]
|
6.46273e-05
|
|
|
KCNMB1
|
[NCBI]
|
5.94295e-05
|
|
|
KCNMA1
|
[NCBI]
|
5.94295e-05
|
|
|
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-positive
|
[NCBI]
|
5.80894e-05
|
|
|
RA
|
[NCBI]
|
5.78441e-05
|
|
|
PLB1
|
[NCBI]
|
5.60554e-05
|
|
|
TLR2
|
[NCBI]
|
5.45873e-05
|
|
|
CEBPE
|
[NCBI]
|
5.15494e-05
|
|
|
XLP1
|
[NCBI]
|
5.12761e-05
|
|
|
DKC
|
[NCBI]
|
5.04472e-05
|
|
|
bare lymphocyte syndrome, type ii
|
[NCBI]
|
4.56234e-05
|
|
|
MYD88
|
[NCBI]
|
4.42288e-05
|
|
|
MBL2
|
[NCBI]
|
4.28771e-05
|
|
|
ELA2
|
[NCBI]
|
4.19344e-05
|
|
|
LSA
|
[NCBI]
|
4.1718e-05
|
|
|
CSF3
|
[NCBI]
|
3.02593e-05
|
|
|
DHFR
|
[NCBI]
|
2.92241e-05
|
|
|
AIRE
|
[NCBI]
|
2.47847e-05
|
|
|
CVID
|
[NCBI]
|
1.74792e-05
|
|
|
hla-d histocompatibility type
|
[NCBI]
|
1.59768e-05
|
|
|
TLR4
|
[NCBI]
|
1.13915e-05
|
|
|
ADA
|
[NCBI]
|
4.88062e-06
|
|
|
CF
|
[NCBI]
|
4.67729e-06
|
|
|
VIP
|
[NCBI]
|
3.83306e-06
|
|
|
CFTR
|
[NCBI]
|
2.9074e-06
|
|
|
APOE
|
[NCBI]
|
4.15875e-07
|
|
|
SLE
|
[NCBI]
|
3.64078e-07
|
|