|
OMIM |
Link |
Information gain |
01 |
|
RA
|
[NCBI]
|
0.0113692
|
|
|
SLE
|
[NCBI]
|
0.00944748
|
|
|
MBP
|
[NCBI]
|
0.00715794
|
|
|
IL2
|
[NCBI]
|
0.00453628
|
|
|
MG
|
[NCBI]
|
0.00299683
|
|
|
IDDM
|
[NCBI]
|
0.00289833
|
|
|
TNFSF6
|
[NCBI]
|
0.00238557
|
|
|
CF
|
[NCBI]
|
0.00235687
|
|
|
CVID
|
[NCBI]
|
0.00224791
|
|
|
hla-d histocompatibility type
|
[NCBI]
|
0.00215219
|
|
|
sjogren syndrome
|
[NCBI]
|
0.00197774
|
|
|
WAS
|
[NCBI]
|
0.0016137
|
|
|
pygmy
|
[NCBI]
|
0.00156309
|
|
|
ADA
|
[NCBI]
|
0.00154658
|
|
|
ALPS
|
[NCBI]
|
0.00142154
|
|
|
alopecia areata 1
|
[NCBI]
|
0.00138102
|
|
|
AD
|
[NCBI]
|
0.00122534
|
|
|
EGF
|
[NCBI]
|
0.00120747
|
|
|
TNF
|
[NCBI]
|
0.00109857
|
|
|
hashimoto thyroiditis
|
[NCBI]
|
0.00104129
|
|
|
psoriasis susceptibility 6
|
[NCBI]
|
0.000844389
|
|
|
candidiasis, familial chronic mucocutaneous, autosomal dominant
|
[NCBI]
|
0.000844389
|
|
|
VRNI
|
[NCBI]
|
0.000828444
|
|
|
IDDM13
|
[NCBI]
|
0.000728301
|
|
|
VEGF
|
[NCBI]
|
0.000682469
|
|
|
LAT
|
[NCBI]
|
0.000654556
|
|
|
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiency
|
[NCBI]
|
0.000617617
|
|
|
cutis laxa, corneal clouding, and mental retardation
|
[NCBI]
|
0.00059798
|
|
|
reticular dysgenesia
|
[NCBI]
|
0.00059798
|
|
|
ehlers-danlos syndrome, type viii
|
[NCBI]
|
0.00059798
|
|
|
pulmonary disease, chronic obstructive
|
[NCBI]
|
0.000554105
|
|
|
TH
|
[NCBI]
|
0.000545595
|
|
|
immune defect due to absence of thymus
|
[NCBI]
|
0.000517837
|
|
|
PSORS4
|
[NCBI]
|
0.000517837
|
|
|