|
OMIM |
Link |
Information gain |
01 |
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
0.0261292
|
|
|
thrombocytopenia, autosomal recessive
|
[NCBI]
|
0.00172954
|
|
|
storage pool platelet disease
|
[NCBI]
|
0.00143921
|
|
|
thrombocytopenia-absent radius syndrome
|
[NCBI]
|
0.00109535
|
|
|
RA
|
[NCBI]
|
0.000887221
|
|
|
GPS
|
[NCBI]
|
0.000432047
|
|
|
hemophagocytic lymphohistiocytosis, familial, 1
|
[NCBI]
|
0.000372668
|
|
|
SLE
|
[NCBI]
|
0.000265528
|
|
|
thrombasthenia of glanzmann and naegeli
|
[NCBI]
|
0.000257193
|
|
|
giant platelet syndrome
|
[NCBI]
|
0.000150239
|
|
|
THC1
|
[NCBI]
|
0.000144794
|
|
|
THC2
|
[NCBI]
|
0.00012757
|
|
|
ITGB3
|
[NCBI]
|
0.000101603
|
|
|
MG
|
[NCBI]
|
7.74588e-05
|
|
|
HPA-2
|
[NCBI]
|
7.59186e-05
|
|
|
autoimmune disease
|
[NCBI]
|
7.32448e-05
|
|
|
LNPEP
|
[NCBI]
|
6.73416e-05
|
|
|
splenomegaly syndrome with splenic germinal center hypoplasia and reduced circulating t-helper cells
|
[NCBI]
|
6.35149e-05
|
|
|
thrombocytopenia, cyclic
|
[NCBI]
|
6.35149e-05
|
|
|
hemangioma-thrombocytopenia syndrome
|
[NCBI]
|
6.07347e-05
|
|
|
PF4
|
[NCBI]
|
5.7744e-05
|
|
|
ETS1
|
[NCBI]
|
5.39023e-05
|
|
|
MME
|
[NCBI]
|
5.19102e-05
|
|
|
GP1BA
|
[NCBI]
|
5.13263e-05
|
|
|
ITGA2B
|
[NCBI]
|
5.13263e-05
|
|
|
EPO
|
[NCBI]
|
4.58642e-05
|
|
|
WAS
|
[NCBI]
|
4.08287e-05
|
|
|
KITLG
|
[NCBI]
|
3.88825e-05
|
|
|
protein c deficiency, congenital thrombotic disease due to
|
[NCBI]
|
3.84125e-05
|
|
|
sea-blue histiocyte disease
|
[NCBI]
|
3.23956e-05
|
|
|
lymphoma, non-hodgkin, familial
|
[NCBI]
|
2.58042e-05
|
|
|
TTP
|
[NCBI]
|
1.92232e-05
|
|
|
ADA
|
[NCBI]
|
1.41129e-05
|
|
|
F3
|
[NCBI]
|
1.21141e-05
|
|
|
WAS
|
[NCBI]
|
9.01292e-06
|
|
|
gaucher disease, type i
|
[NCBI]
|
5.29434e-06
|
|
|
PCNA
|
[NCBI]
|
4.55026e-06
|
|
|
CVID
|
[NCBI]
|
2.86829e-06
|
|
|
DBA
|
[NCBI]
|
1.70345e-06
|
|