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01 Blood Platelet Disorders [NCBI]

Gene


 Gene Link Information
Gain		 01
WFS2 [NCBI] 0.000438875
MYH9 [NCBI] 0.0001343
VWF [NCBI] 9.78387e-05
RUNX1 [NCBI] 6.7237e-05
PF4 [NCBI] 4.41983e-05
ITGB3 [NCBI] 3.71341e-05
GP1BB [NCBI] 2.2304e-05
MPL [NCBI] 2.0409e-05
PLEK [NCBI] 1.72309e-05
ITGA2B [NCBI] 1.48886e-05
MMRN1 [NCBI] 1.27902e-05
GP5 [NCBI] 1.17731e-05
MYH10 [NCBI] 1.08941e-05
WAS [NCBI] 1.06745e-05
GNAQ [NCBI] 9.88476e-06
TBXAS1 [NCBI] 9.76214e-06
HOXA11 [NCBI] 9.43956e-06
TBXA2R [NCBI] 9.34426e-06
GP9 [NCBI] 9.00865e-06
GNAI2 [NCBI] 8.60356e-06
PTGS1 [NCBI] 8.46324e-06
NFE2 [NCBI] 8.22742e-06
HOXA10 [NCBI] 8.17987e-06
P2RY12 [NCBI] 7.96014e-06
CBFB [NCBI] 7.84072e-06
HPS1 [NCBI] 7.558e-06
GP1BA [NCBI] 6.68596e-06
THBS1 [NCBI] 6.41647e-06
ITGAV [NCBI] 6.25808e-06
EPB41L1 [NCBI] 6.0321e-06
EPB41L2 [NCBI] 5.85658e-06
GNB3 [NCBI] 5.66555e-06
FCGR2A [NCBI] 5.65497e-06
IBSP [NCBI] 5.29567e-06
GATA1 [NCBI] 5.1807e-06
F2 [NCBI] 3.67204e-06
F5 [NCBI] 3.32901e-06
PTGS2 [NCBI] 3.2149e-06
JAK2 [NCBI] 2.85434e-06
ACHE [NCBI] 2.25028e-06
MTHFR [NCBI] 2.21271e-06
NPY [NCBI] 1.9489e-06
MPO [NCBI] 1.37396e-06
EGF [NCBI] 6.10966e-07



OMIM


 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



Database Center for Life Science