|
OMIM |
Link |
Information gain |
01 |
|
IGAN1
|
[NCBI]
|
0.0233201
|
|
|
IGAD1
|
[NCBI]
|
0.0133935
|
|
|
CD
|
[NCBI]
|
0.00804655
|
|
|
immunoglobulin m, level of
|
[NCBI]
|
0.00222932
|
|
|
reticular dysgenesia
|
[NCBI]
|
0.00130315
|
|
|
RA
|
[NCBI]
|
0.00126982
|
|
|
dubowitz syndrome
|
[NCBI]
|
0.00110861
|
|
|
PIGR
|
[NCBI]
|
0.000966605
|
|
|
pulmonary alveolar proteinosis, acquired
|
[NCBI]
|
0.0008179
|
|
|
CVID
|
[NCBI]
|
0.000785811
|
|
|
WM1
|
[NCBI]
|
0.000623172
|
|
|
SLE
|
[NCBI]
|
0.000528451
|
|
|
HIGM1
|
[NCBI]
|
0.000404037
|
|
|
FCAR
|
[NCBI]
|
0.000235698
|
|
|
RNASE3
|
[NCBI]
|
0.000182477
|
|
|
myeloma, multiple
|
[NCBI]
|
0.000176239
|
|
|
secretory component deficiency
|
[NCBI]
|
0.000165895
|
|
|
MG
|
[NCBI]
|
0.000147882
|
|
|
gamma-a-globulin, defect in assembly of
|
[NCBI]
|
0.000104571
|
|
|
epilepsy-telangiectasia
|
[NCBI]
|
0.000104571
|
|
|
combined inflammatory and immunologic defect
|
[NCBI]
|
0.000104571
|
|
|
immune deficiency, familial variable
|
[NCBI]
|
0.000104571
|
|
|
thrombocytopenia with elevated serum iga and renal disease
|
[NCBI]
|
0.000104571
|
|
|
lymphokine deficiency
|
[NCBI]
|
0.000104571
|
|
|
diarrhea, glucose-stimulated secretory, with common variable immunodeficiency
|
[NCBI]
|
0.000104571
|
|
|
fc fragment of iga and igm, receptor for
|
[NCBI]
|
7.45282e-05
|
|
|
dermographism, familial
|
[NCBI]
|
7.3213e-05
|
|
|
persistent polyclonal b-cell lymphocytosis
|
[NCBI]
|
7.3213e-05
|
|
|
panencephalitis, subacute sclerosing
|
[NCBI]
|
7.03597e-05
|
|
|
MBL2
|
[NCBI]
|
6.27961e-05
|
|
|
dermatitis herpetiformis, familial
|
[NCBI]
|
6.15218e-05
|
|
|
hypoproteinemia, hypercatabolic
|
[NCBI]
|
6.15218e-05
|
|
|
chromosome 18p deletion syndrome
|
[NCBI]
|
6.15218e-05
|
|
|
icos deficiency
|
[NCBI]
|
6.15218e-05
|
|
|
hyperimmunoglobulin g1(a1) syndrome
|
[NCBI]
|
6.15218e-05
|
|
|
MBP
|
[NCBI]
|
6.14194e-05
|
|
|
CF
|
[NCBI]
|
5.84905e-05
|
|
|
IGKC
|
[NCBI]
|
5.76447e-05
|
|
|
hyperimmunoglobulin e recurrent infection syndrome, autosomal dominant
|
[NCBI]
|
5.74139e-05
|
|
|
IL5
|
[NCBI]
|
5.49517e-05
|
|
|
IGHA2
|
[NCBI]
|
5.40975e-05
|
|
|
IGAD2
|
[NCBI]
|
5.40111e-05
|
|
|
vitiligo
|
[NCBI]
|
5.40111e-05
|
|
|
ear wax, wet/dry
|
[NCBI]
|
5.40111e-05
|
|
|
CEACAM5
|
[NCBI]
|
5.35641e-05
|
|
|
AT
|
[NCBI]
|
5.13211e-05
|
|
|
GBS
|
[NCBI]
|
4.84858e-05
|
|
|
IGHE
|
[NCBI]
|
4.56261e-05
|
|
|
ectodermal dysplasia, hypohidrotic, with immune deficiency
|
[NCBI]
|
4.413e-05
|
|
|
hypogammaglobulinemia and isolated growth hormone deficiency, x-linked
|
[NCBI]
|
4.413e-05
|
|
|
GS2
|
[NCBI]
|
4.05468e-05
|
|
|
cyclic hematopoiesis
|
[NCBI]
|
4.05468e-05
|
|
|
MAG
|
[NCBI]
|
3.97628e-05
|
|
|
heart block, congenital
|
[NCBI]
|
3.75129e-05
|
|
|
GS1
|
[NCBI]
|
3.75129e-05
|
|
|
mulibrey nanism
|
[NCBI]
|
3.75129e-05
|
|
|
AICDA
|
[NCBI]
|
3.53226e-05
|
|
|
NPS
|
[NCBI]
|
3.52404e-05
|
|
|
CD40LG
|
[NCBI]
|
3.42831e-05
|
|
|
TF
|
[NCBI]
|
3.42399e-05
|
|
|
HHS
|
[NCBI]
|
3.25849e-05
|
|
|
DSG1
|
[NCBI]
|
3.06969e-05
|
|
|
CCL28
|
[NCBI]
|
2.98352e-05
|
|
|
RAB3B
|
[NCBI]
|
2.98352e-05
|
|
|
IGHG1
|
[NCBI]
|
2.89848e-05
|
|
|
APCS
|
[NCBI]
|
2.73505e-05
|
|
|
MAL2
|
[NCBI]
|
2.70383e-05
|
|
|
IHG
|
[NCBI]
|
2.70383e-05
|
|
|
IGJ
|
[NCBI]
|
2.70383e-05
|
|
|
VEGF
|
[NCBI]
|
2.614e-05
|
|
|
lymphoma, non-hodgkin, familial
|
[NCBI]
|
2.57784e-05
|
|
|
RAB11FIP2
|
[NCBI]
|
2.52238e-05
|
|
|
IGHA1
|
[NCBI]
|
2.52238e-05
|
|
|
MADCAM1
|
[NCBI]
|
2.52238e-05
|
|
|
IL10
|
[NCBI]
|
2.45838e-05
|
|
|
UGB
|
[NCBI]
|
2.36156e-05
|
|
|
IBD1
|
[NCBI]
|
2.28341e-05
|
|
|
SCN1
|
[NCBI]
|
2.28186e-05
|
|
|
LTBR
|
[NCBI]
|
2.19111e-05
|
|
|
EGF
|
[NCBI]
|
2.15038e-05
|
|
|
BCGF
|
[NCBI]
|
2.1271e-05
|
|
|
TNFSF14
|
[NCBI]
|
2.11486e-05
|
|
|
FMF
|
[NCBI]
|
2.10243e-05
|
|
|
complement factor h deficiency
|
[NCBI]
|
2.05175e-05
|
|
|
hodgkin lymphoma
|
[NCBI]
|
2.05175e-05
|
|
|
pituitary dwarfism i
|
[NCBI]
|
2.05175e-05
|
|
|
FCGRT
|
[NCBI]
|
2.04826e-05
|
|
|
PRKCD
|
[NCBI]
|
2.04826e-05
|
|
|
TNFSF13
|
[NCBI]
|
1.98915e-05
|
|
|
TNFRSF13C
|
[NCBI]
|
1.98915e-05
|
|
|
DSC3
|
[NCBI]
|
1.98915e-05
|
|
|
HAVCR1
|
[NCBI]
|
1.98915e-05
|
|
|
XLP1
|
[NCBI]
|
1.94835e-05
|
|
|
SMAD7
|
[NCBI]
|
1.93602e-05
|
|
|
DSC1
|
[NCBI]
|
1.93602e-05
|
|
|
CXCL10
|
[NCBI]
|
1.93602e-05
|
|
|
AFP
|
[NCBI]
|
1.89213e-05
|
|
|
AMBP
|
[NCBI]
|
1.88778e-05
|
|
|
ICOS
|
[NCBI]
|
1.80289e-05
|
|
|
NGFB
|
[NCBI]
|
1.76311e-05
|
|
|
MPO
|
[NCBI]
|
1.67447e-05
|
|
|
SMAD3
|
[NCBI]
|
1.66591e-05
|
|
|
IL7
|
[NCBI]
|
1.66591e-05
|
|
|
LTF
|
[NCBI]
|
1.66591e-05
|
|
|
TGM2
|
[NCBI]
|
1.60896e-05
|
|
|
CCL25
|
[NCBI]
|
1.55769e-05
|
|
|
HIDS
|
[NCBI]
|
1.51944e-05
|
|
|
TNF
|
[NCBI]
|
1.51754e-05
|
|
|
CRIP1
|
[NCBI]
|
1.51106e-05
|
|
|
COL17A1
|
[NCBI]
|
1.39234e-05
|
|
|
immunodeficiency-centromeric instability-facial anomalies syndrome
|
[NCBI]
|
1.37983e-05
|
|
|
glycogen storage disease ib
|
[NCBI]
|
1.37983e-05
|
|
|
TNFSF8
|
[NCBI]
|
1.35823e-05
|
|
|
NOS2A
|
[NCBI]
|
1.35823e-05
|
|
|
DNMT3B
|
[NCBI]
|
1.31104e-05
|
|
|
IKBKG
|
[NCBI]
|
1.29624e-05
|
|
|
APS1
|
[NCBI]
|
1.28585e-05
|
|
|
ALB
|
[NCBI]
|
1.27447e-05
|
|
|
granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type i
|
[NCBI]
|
1.25429e-05
|
|
|
PTPRC
|
[NCBI]
|
1.21567e-05
|
|
|
ARF6
|
[NCBI]
|
1.17982e-05
|
|
|
USF1
|
[NCBI]
|
1.16843e-05
|
|
|
DMPK
|
[NCBI]
|
1.13576e-05
|
|
|
CCL21
|
[NCBI]
|
1.11514e-05
|
|
|
PI
|
[NCBI]
|
1.11394e-05
|
|
|
PRL
|
[NCBI]
|
1.05595e-05
|
|
|
PROCR
|
[NCBI]
|
1.04919e-05
|
|
|
CFB
|
[NCBI]
|
1.0319e-05
|
|
|
EGFR
|
[NCBI]
|
1.02791e-05
|
|
|
TG
|
[NCBI]
|
9.32764e-06
|
|
|
BTK
|
[NCBI]
|
8.68597e-06
|
|
|
PTH
|
[NCBI]
|
8.47313e-06
|
|
|
CCL17
|
[NCBI]
|
8.2855e-06
|
|
|
TPO
|
[NCBI]
|
7.87035e-06
|
|
|
CCL22
|
[NCBI]
|
7.81823e-06
|
|
|
aHUS
|
[NCBI]
|
7.43504e-06
|
|
|
NSF
|
[NCBI]
|
7.30733e-06
|
|
|
IL4
|
[NCBI]
|
7.30733e-06
|
|
|
WAS
|
[NCBI]
|
6.70272e-06
|
|
|
HP
|
[NCBI]
|
6.50797e-06
|
|
|
RNASE2
|
[NCBI]
|
6.36833e-06
|
|
|
PG
|
[NCBI]
|
6.23062e-06
|
|
|
BL
|
[NCBI]
|
5.86052e-06
|
|
|
LPO
|
[NCBI]
|
5.81307e-06
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
4.90672e-06
|
|
|
IL6
|
[NCBI]
|
4.87168e-06
|
|
|
BDNF
|
[NCBI]
|
4.77636e-06
|
|
|
RDT
|
[NCBI]
|
4.74281e-06
|
|
|
ADA
|
[NCBI]
|
4.64143e-06
|
|
|
CHH
|
[NCBI]
|
4.04558e-06
|
|
|
COMP
|
[NCBI]
|
3.54573e-06
|
|
|
TTR
|
[NCBI]
|
3.52152e-06
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
3.3275e-06
|
|
|
CDK2
|
[NCBI]
|
3.21218e-06
|
|
|
APOE
|
[NCBI]
|
2.92545e-06
|
|
|
OCP
|
[NCBI]
|
2.11599e-06
|
|
|
VIP
|
[NCBI]
|
2.06116e-06
|
|
|
CHS
|
[NCBI]
|
1.62611e-06
|
|
|
porphyria variegata
|
[NCBI]
|
1.39182e-06
|
|
|
PCNA
|
[NCBI]
|
1.35724e-06
|
|
|
ACE
|
[NCBI]
|
1.15666e-06
|
|
|
hla-d histocompatibility type
|
[NCBI]
|
8.61998e-07
|
|
|
IL2
|
[NCBI]
|
6.13017e-07
|
|
|
SOD2
|
[NCBI]
|
5.99183e-07
|
|
|
MUC1
|
[NCBI]
|
4.75316e-07
|
|
|
CCK
|
[NCBI]
|
2.76166e-07
|
|
|
HGF
|
[NCBI]
|
2.61417e-07
|
|
|
PCD
|
[NCBI]
|
2.32533e-07
|
|
|
CNTF
|
[NCBI]
|
1.34504e-07
|
|
|
EPO
|
[NCBI]
|
1.22164e-07
|
|
|
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiency
|
[NCBI]
|
8.7272e-08
|
|
|
WBS
|
[NCBI]
|
4.95781e-08
|
|
|
CFTR
|
[NCBI]
|
1.47329e-08
|
|
|
SPP1
|
[NCBI]
|
3.68165e-09
|
|