|
OMIM |
Link |
Information gain |
01 |
|
NCR
|
[NCBI]
|
0.000991404
|
|
|
lymphangiectasia, intestinal
|
[NCBI]
|
0.000991404
|
|
|
MBP
|
[NCBI]
|
0.000878571
|
|
|
immune defect due to absence of thymus
|
[NCBI]
|
0.000798231
|
|
|
hla-d histocompatibility type
|
[NCBI]
|
0.000279284
|
|
|
immunodeficiency with defective leukocyte and lymphocyte function and with response to histamine-1 antagonist
|
[NCBI]
|
0.000188729
|
|
|
IL2
|
[NCBI]
|
0.000180341
|
|
|
GS1
|
[NCBI]
|
0.000152627
|
|
|
GS2
|
[NCBI]
|
0.000146123
|
|
|
TNF
|
[NCBI]
|
0.000131349
|
|
|
TNFSF6
|
[NCBI]
|
0.000117657
|
|
|
atypical mycobacteriosis, familial
|
[NCBI]
|
0.000117163
|
|
|
fanconi-like syndrome
|
[NCBI]
|
0.000116703
|
|
|
lymphoblastic transformation, intrinsic defect in
|
[NCBI]
|
0.000116703
|
|
|
lymphoid system deterioration, progressive
|
[NCBI]
|
0.000116703
|
|
|
monocyte chemotactic disorder
|
[NCBI]
|
0.000116703
|
|
|
lymphokine deficiency
|
[NCBI]
|
0.000116703
|
|
|
granulomatous disease due to combined cellular and humoral immune defects
|
[NCBI]
|
0.000116703
|
|
|
lymphoblastic transformation, inhibition of
|
[NCBI]
|
0.000116703
|
|
|
retinal telangiectasia and hypogammaglobulinemia
|
[NCBI]
|
0.000116703
|
|
|
ataxic diplegia with defective cellular immunity
|
[NCBI]
|
9.42421e-05
|
|
|
urticaria, familial localized heat
|
[NCBI]
|
9.42421e-05
|
|
|
MIF
|
[NCBI]
|
8.15132e-05
|
|
|
dermographism, familial
|
[NCBI]
|
8.02756e-05
|
|
|
microcephaly with chemotactic defect and transient hypogammaglobulinemia
|
[NCBI]
|
8.02756e-05
|
|
|
CD44
|
[NCBI]
|
7.979e-05
|
|
|
RNASE3
|
[NCBI]
|
7.94637e-05
|
|
|
AT
|
[NCBI]
|
7.76658e-05
|
|
|
VIP
|
[NCBI]
|
7.31965e-05
|
|
|
complement factor i deficiency
|
[NCBI]
|
6.79255e-05
|
|
|
RA
|
[NCBI]
|
6.77362e-05
|
|
|
IL12B
|
[NCBI]
|
6.61243e-05
|
|
|
CEACAM5
|
[NCBI]
|
5.3894e-05
|
|
|
prostaglandin d2 synthase, hematopoietic
|
[NCBI]
|
5.37745e-05
|
|
|
IRAK1
|
[NCBI]
|
5.37745e-05
|
|
|
FOXP3
|
[NCBI]
|
5.26042e-05
|
|
|
STAT6
|
[NCBI]
|
5.26042e-05
|
|
|
HNA
|
[NCBI]
|
4.95931e-05
|
|
|
BIRC7
|
[NCBI]
|
4.85842e-05
|
|
|
SEMA7A
|
[NCBI]
|
4.85842e-05
|
|
|
CD74
|
[NCBI]
|
4.85842e-05
|
|
|
CD
|
[NCBI]
|
4.69784e-05
|
|
|
MGAT5
|
[NCBI]
|
4.52175e-05
|
|
|
PTGES
|
[NCBI]
|
4.52175e-05
|
|
|
CCR6
|
[NCBI]
|
4.27168e-05
|
|
|
DKC
|
[NCBI]
|
4.13666e-05
|
|
|
VEGF
|
[NCBI]
|
3.81653e-05
|
|
|
IL12RB1
|
[NCBI]
|
3.7659e-05
|
|
|
ABP1
|
[NCBI]
|
3.62984e-05
|
|
|
MYO5A
|
[NCBI]
|
3.53286e-05
|
|
|
IL17A
|
[NCBI]
|
3.43439e-05
|
|
|
IL12A
|
[NCBI]
|
3.26318e-05
|
|
|
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiency
|
[NCBI]
|
3.21321e-05
|
|
|
RAB27A
|
[NCBI]
|
3.18775e-05
|
|
|
APS1
|
[NCBI]
|
2.65214e-05
|
|
|
SLE
|
[NCBI]
|
2.41705e-05
|
|
|
PTH
|
[NCBI]
|
1.88732e-05
|
|
|
CCL2
|
[NCBI]
|
1.84583e-05
|
|
|
CHS
|
[NCBI]
|
1.69707e-05
|
|
|
TERT
|
[NCBI]
|
1.48696e-05
|
|
|
WAS
|
[NCBI]
|
1.14102e-05
|
|
|
IFNA1
|
[NCBI]
|
1.07539e-05
|
|
|
F3
|
[NCBI]
|
1.04531e-05
|
|
|
KLK3
|
[NCBI]
|
9.49484e-06
|
|
|
PRL
|
[NCBI]
|
9.37274e-06
|
|
|
SPP1
|
[NCBI]
|
8.18858e-06
|
|
|
CYP1A1
|
[NCBI]
|
7.17025e-06
|
|
|
NGFB
|
[NCBI]
|
6.37312e-06
|
|
|
MBL2
|
[NCBI]
|
5.79847e-06
|
|
|
MG
|
[NCBI]
|
4.03524e-06
|
|
|
PF4
|
[NCBI]
|
3.23066e-06
|
|
|
CAT
|
[NCBI]
|
1.67528e-06
|
|
|
CRC
|
[NCBI]
|
1.44731e-06
|
|
|
CRH
|
[NCBI]
|
1.39634e-06
|
|
|
MPO
|
[NCBI]
|
6.24371e-07
|
|
|
TNFRSF11B
|
[NCBI]
|
5.97488e-07
|
|
|
ADA
|
[NCBI]
|
4.12112e-08
|
|