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01 Hemorrhagic Disorders [NCBI]


Gene


Gene Link Information
Gain
01
VWF [NCBI] 0.000110323
SERPINF2 [NCBI] 3.6084e-05
VKORC1 [NCBI] 2.61693e-05
F8 [NCBI] 1.84094e-05
HPS1 [NCBI] 1.80032e-05
PLEK [NCBI] 1.76885e-05
ADAMTS13 [NCBI] 1.74315e-05
F13A1 [NCBI] 1.53452e-05
F3 [NCBI] 1.51683e-05
FGB [NCBI] 1.48138e-05
F7 [NCBI] 1.46619e-05
SERPINA1 [NCBI] 1.32781e-05
MMRN1 [NCBI] 1.30177e-05
GGCX [NCBI] 1.02442e-05
F2 [NCBI] 1.01222e-05
GNAQ [NCBI] 1.01121e-05
SERPINE1 [NCBI] 9.89897e-06
THBS2 [NCBI] 9.7678e-06
GP9 [NCBI] 9.23586e-06
GNAI2 [NCBI] 8.83066e-06
F10 [NCBI] 8.83066e-06
LYST [NCBI] 8.18699e-06
F11 [NCBI] 8.10642e-06
FGG [NCBI] 7.88531e-06
FGA [NCBI] 7.03318e-06
MYH9 [NCBI] 6.91197e-06
ITGA2B [NCBI] 6.46857e-06
ITGA2 [NCBI] 6.40961e-06
GNAS [NCBI] 5.44465e-06
GATA1 [NCBI] 5.40441e-06
MPL [NCBI] 5.13354e-06
ITGB3 [NCBI] 4.8603e-06
CYP2C9 [NCBI] 4.8489e-06
TFPI [NCBI] 4.3074e-06
F5 [NCBI] 3.5447e-06
IL1B [NCBI] 3.26652e-06
JAK2 [NCBI] 3.06592e-06
PLAUR [NCBI] 2.88901e-06
IL6 [NCBI] 2.43626e-06
IL1RN [NCBI] 2.15056e-06
NOS2 [NCBI] 2.12656e-06
TNF [NCBI] 1.55555e-07




OMIM


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




Database Center for Life Science