|
OMIM |
Link |
Information gain |
01 |
|
HPS
|
[NCBI]
|
0.00113811
|
|
|
QPD
|
[NCBI]
|
0.000764597
|
|
|
scott syndrome
|
[NCBI]
|
0.000684465
|
|
|
GPS
|
[NCBI]
|
0.000550304
|
|
|
thrombocytopenia-absent radius syndrome
|
[NCBI]
|
0.000545114
|
|
|
factor x deficiency
|
[NCBI]
|
0.000346733
|
|
|
plasmin inhibitor deficiency
|
[NCBI]
|
0.000308343
|
|
|
FGA
|
[NCBI]
|
0.000259388
|
|
|
vitamin k-dependent clotting factors, combined deficiency of, 1
|
[NCBI]
|
0.000244728
|
|
|
F2
|
[NCBI]
|
0.000224404
|
|
|
passovoy factor
|
[NCBI]
|
0.000210436
|
|
|
ehlers-danlos syndrome, type i
|
[NCBI]
|
0.00019273
|
|
|
factor v deficiency
|
[NCBI]
|
0.000150621
|
|
|
F5F8D
|
[NCBI]
|
0.000148417
|
|
|
afibrinogenemia, congenital
|
[NCBI]
|
0.000141703
|
|
|
pta deficiency
|
[NCBI]
|
0.00012993
|
|
|
hemangioma-thrombocytopenia syndrome
|
[NCBI]
|
0.000128619
|
|
|
F13A1
|
[NCBI]
|
0.000123972
|
|
|
fibrinolytic defect
|
[NCBI]
|
0.000120535
|
|
|
hemophilia a with vascular abnormality
|
[NCBI]
|
0.000120535
|
|
|
factor vii deficiency
|
[NCBI]
|
0.000117127
|
|
|
F3
|
[NCBI]
|
9.94889e-05
|
|
|
von willebrand disease
|
[NCBI]
|
8.98164e-05
|
|
|
vitamin k-dependent clotting factors, combined deficiency of, 2
|
[NCBI]
|
8.95989e-05
|
|
|
athrombia, essential
|
[NCBI]
|
8.95989e-05
|
|
|
thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis
|
[NCBI]
|
8.95989e-05
|
|
|
platelet disorder, familial, with associated myeloid malignancy
|
[NCBI]
|
8.00136e-05
|
|
|
HEMB
|
[NCBI]
|
7.93267e-05
|
|
|
anemia, autoimmune hemolytic
|
[NCBI]
|
7.6759e-05
|
|
|
TMAU
|
[NCBI]
|
6.34987e-05
|
|
|
MMRN1
|
[NCBI]
|
6.26498e-05
|
|
|
THBS2
|
[NCBI]
|
6.26498e-05
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
5.95316e-05
|
|
|
THC2
|
[NCBI]
|
5.80895e-05
|
|
|
anemia, dyserythropoietic congenital, type i
|
[NCBI]
|
5.80895e-05
|
|
|
PROZ
|
[NCBI]
|
5.74529e-05
|
|
|
PLCB2
|
[NCBI]
|
5.40796e-05
|
|
|
CD63
|
[NCBI]
|
5.40796e-05
|
|
|
TTP
|
[NCBI]
|
5.20612e-05
|
|
|
VKORC1
|
[NCBI]
|
5.15724e-05
|
|
|
GGCX
|
[NCBI]
|
4.316e-05
|
|
|
FGB
|
[NCBI]
|
4.22596e-05
|
|
|
HPS1
|
[NCBI]
|
4.22596e-05
|
|
|
PLAT
|
[NCBI]
|
4.06738e-05
|
|
|
ABL
|
[NCBI]
|
3.83867e-05
|
|
|
PI
|
[NCBI]
|
3.71458e-05
|
|
|
FGG
|
[NCBI]
|
3.56351e-05
|
|
|
gaucher disease, type i
|
[NCBI]
|
3.43352e-05
|
|
|
PAI1
|
[NCBI]
|
3.36626e-05
|
|
|
thrombasthenia of glanzmann and naegeli
|
[NCBI]
|
3.23136e-05
|
|
|
PIGA
|
[NCBI]
|
3.14398e-05
|
|
|
NS1
|
[NCBI]
|
3.10017e-05
|
|
|
giant platelet syndrome
|
[NCBI]
|
2.97992e-05
|
|
|
PCI
|
[NCBI]
|
2.83197e-05
|
|
|
CPB2
|
[NCBI]
|
2.50608e-05
|
|
|
GNAS
|
[NCBI]
|
2.31067e-05
|
|
|
CHS
|
[NCBI]
|
2.02919e-05
|
|
|
hemophilia a
|
[NCBI]
|
1.65569e-05
|
|
|
SLE
|
[NCBI]
|
9.23542e-06
|
|
|
TFPI
|
[NCBI]
|
8.72472e-06
|
|
|
APOB
|
[NCBI]
|
6.05684e-06
|
|