|
OMIM |
Link |
Information gain |
01 |
|
GPS
|
[NCBI]
|
0.0166892
|
|
|
storage pool platelet disease
|
[NCBI]
|
0.00579564
|
|
|
QPD
|
[NCBI]
|
0.00437605
|
|
|
thrombasthenia of glanzmann and naegeli
|
[NCBI]
|
0.00264349
|
|
|
thrombasthenia-thrombocytopenia, hereditary
|
[NCBI]
|
0.00252422
|
|
|
giant platelet syndrome
|
[NCBI]
|
0.0017754
|
|
|
scott syndrome
|
[NCBI]
|
0.00142731
|
|
|
prostaglandin-endoperoxide synthase deficiency
|
[NCBI]
|
0.00137971
|
|
|
MHA
|
[NCBI]
|
0.000878511
|
|
|
acute myelogenous leukemia
|
[NCBI]
|
0.000620619
|
|
|
HPS
|
[NCBI]
|
0.000610291
|
|
|
SBS
|
[NCBI]
|
0.000311267
|
|
|
MYH9
|
[NCBI]
|
0.00029227
|
|
|
platelet disorder, familial, with associated myeloid malignancy
|
[NCBI]
|
0.000266292
|
|
|
von willebrand disease
|
[NCBI]
|
0.000250417
|
|
|
epstein syndrome
|
[NCBI]
|
0.000216487
|
|
|
glanzmann thrombasthenia, autosomal dominant
|
[NCBI]
|
0.000213732
|
|
|
ITGB3
|
[NCBI]
|
0.000196842
|
|
|
FTNS
|
[NCBI]
|
0.000195916
|
|
|
PF4
|
[NCBI]
|
0.000187811
|
|
|
JBS
|
[NCBI]
|
0.000186809
|
|
|
athrombia, essential
|
[NCBI]
|
0.000182799
|
|
|
TCPT
|
[NCBI]
|
0.000159248
|
|
|
SLE
|
[NCBI]
|
0.000154417
|
|
|
THC2
|
[NCBI]
|
0.000112298
|
|
|
primary release disorder of platelets
|
[NCBI]
|
0.000106799
|
|
|
platelet aggregation, spontaneous
|
[NCBI]
|
0.000106799
|
|
|
platelet prostacyclin receptor defect
|
[NCBI]
|
0.000106799
|
|
|
hemophilia a with vascular abnormality
|
[NCBI]
|
0.000106799
|
|
|
platelet signal processing defect
|
[NCBI]
|
0.000106799
|
|
|
platelet factor 3 deficiency
|
[NCBI]
|
0.000106799
|
|
|
platelet responsiveness to adrenaline, depressed
|
[NCBI]
|
0.000106799
|
|
|
giant platelet syndrome with thrombocytopenia
|
[NCBI]
|
0.000106799
|
|
|
platelet disorder, undefined
|
[NCBI]
|
0.000106799
|
|
|
ITGA2B
|
[NCBI]
|
9.96173e-05
|
|
|
WAS
|
[NCBI]
|
8.89029e-05
|
|
|
ehlers-danlos syndrome with platelet dysfunction from fibronectin abnormality
|
[NCBI]
|
8.4349e-05
|
|
|
MYH10
|
[NCBI]
|
8.08766e-05
|
|
|
bernard-soulier syndrome, benign autosomal dominant
|
[NCBI]
|
7.5889e-05
|
|
|
thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis
|
[NCBI]
|
7.5889e-05
|
|
|
CHS
|
[NCBI]
|
7.23843e-05
|
|
|
factor v deficiency
|
[NCBI]
|
6.99994e-05
|
|
|
MMRN1
|
[NCBI]
|
6.70987e-05
|
|
|
HPA-2
|
[NCBI]
|
6.70987e-05
|
|
|
PMF
|
[NCBI]
|
6.30874e-05
|
|
|
PLCB2
|
[NCBI]
|
5.85252e-05
|
|
|
RABGGTA
|
[NCBI]
|
5.85252e-05
|
|
|
GP1BB
|
[NCBI]
|
5.85252e-05
|
|
|
TBXA2R
|
[NCBI]
|
5.2356e-05
|
|
|
HHS
|
[NCBI]
|
4.86905e-05
|
|
|
FLI1
|
[NCBI]
|
4.75941e-05
|
|
|
ABO
|
[NCBI]
|
4.58656e-05
|
|
|
erythermalgia, primary
|
[NCBI]
|
4.45711e-05
|
|
|
GP1BA
|
[NCBI]
|
4.25339e-05
|
|
|
CFB
|
[NCBI]
|
4.25339e-05
|
|
|
TTP
|
[NCBI]
|
3.86449e-05
|
|
|
PPH1
|
[NCBI]
|
3.74653e-05
|
|
|
lecithin:cholesterol acyltransferase deficiency
|
[NCBI]
|
3.74653e-05
|
|
|
polycythemia vera
|
[NCBI]
|
3.74653e-05
|
|
|
glycogen storage disease ib
|
[NCBI]
|
3.63716e-05
|
|
|
RUNX1
|
[NCBI]
|
3.45034e-05
|
|
|
neuraminidase deficiency with beta-galactosidase deficiency
|
[NCBI]
|
3.37843e-05
|
|
|
antithrombin iii deficiency
|
[NCBI]
|
2.56882e-05
|
|
|
BCHE
|
[NCBI]
|
2.43088e-05
|
|
|
F3
|
[NCBI]
|
2.10985e-05
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
1.90585e-05
|
|
|
VEGF
|
[NCBI]
|
4.69142e-06
|
|
|
ACHE
|
[NCBI]
|
3.48023e-06
|
|
|
NPY
|
[NCBI]
|
2.3605e-06
|
|
|
MPO
|
[NCBI]
|
7.14144e-07
|
|
|
EGF
|
[NCBI]
|
3.07512e-07
|
|