|
OMIM |
Link |
Information gain |
01 |
|
WAS
|
[NCBI]
|
0.0285102
|
|
|
WAS
|
[NCBI]
|
0.00321586
|
|
|
GPS
|
[NCBI]
|
0.000902463
|
|
|
THC1
|
[NCBI]
|
0.000705849
|
|
|
WIPF1
|
[NCBI]
|
0.000689257
|
|
|
SPN
|
[NCBI]
|
0.000194954
|
|
|
wiskott-aldrich syndrome
|
[NCBI]
|
0.000185325
|
|
|
IPEX
|
[NCBI]
|
0.000139414
|
|
|
WASL
|
[NCBI]
|
0.000133141
|
|
|
WASF1
|
[NCBI]
|
0.000133141
|
|
|
SXI1
|
[NCBI]
|
0.000108417
|
|
|
XLN
|
[NCBI]
|
9.26351e-05
|
|
|
SLC35A2
|
[NCBI]
|
7.59874e-05
|
|
|
transducer of cdc42-dependent actin assembly 1
|
[NCBI]
|
7.59874e-05
|
|
|
anemia, sideroblastic, x-linked
|
[NCBI]
|
7.43981e-05
|
|
|
FOXP3
|
[NCBI]
|
6.92736e-05
|
|
|
hypoproteinemia, hypercatabolic
|
[NCBI]
|
6.17872e-05
|
|
|
FCGRT
|
[NCBI]
|
5.70147e-05
|
|
|
C3ORF10
|
[NCBI]
|
5.70147e-05
|
|
|
NCK1
|
[NCBI]
|
5.70147e-05
|
|
|
CRKL
|
[NCBI]
|
5.36416e-05
|
|
|
MSN
|
[NCBI]
|
5.11345e-05
|
|
|
CDC42
|
[NCBI]
|
4.74778e-05
|
|
|
ZAP70
|
[NCBI]
|
4.60576e-05
|
|
|
RAC1
|
[NCBI]
|
4.18232e-05
|
|
|
SYP
|
[NCBI]
|
4.18232e-05
|
|
|
properdin deficiency, x-linked
|
[NCBI]
|
3.61268e-05
|
|
|
VASP
|
[NCBI]
|
3.18984e-05
|
|
|
NP
|
[NCBI]
|
3.10082e-05
|
|
|
G6PD
|
[NCBI]
|
2.99704e-05
|
|
|
SH2D1A
|
[NCBI]
|
2.89728e-05
|
|
|
DMPK
|
[NCBI]
|
2.80975e-05
|
|
|
B2M
|
[NCBI]
|
2.62084e-05
|
|
|
hyperimmunoglobulin e recurrent infection syndrome, autosomal dominant
|
[NCBI]
|
2.46911e-05
|
|
|
ichthyosis, x-linked
|
[NCBI]
|
2.24531e-05
|
|
|
CVID
|
[NCBI]
|
1.7267e-05
|
|
|
SCIDX1
|
[NCBI]
|
1.63532e-05
|
|
|
CHS
|
[NCBI]
|
1.42129e-05
|
|
|
hla-d histocompatibility type
|
[NCBI]
|
1.3778e-05
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
1.02006e-05
|
|
|
AT
|
[NCBI]
|
4.96844e-06
|
|
|
EGF
|
[NCBI]
|
3.43869e-06
|
|
|
ADA
|
[NCBI]
|
3.29966e-06
|
|
|
HPS
|
[NCBI]
|
3.01131e-06
|
|
|
EGFR
|
[NCBI]
|
1.40595e-06
|
|