hemorrhage Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description loss of blood from the vascular compartment to the exterior or into nonvascular body space as a result of rupture or severance of the blood vessels (Mammalian Phenotype Ontology, MP_0001914)
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Genes

9 genes associated with the disease hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
CYP2C9 cytochrome P450, family 2, subfamily C, polypeptide 9
F12 coagulation factor XII (Hageman factor)
F2R coagulation factor II (thrombin) receptor
GP6 glycoprotein VI (platelet)
ITGA2 integrin, alpha 2 (CD49B, alpha 2 subunit of VLA-2 receptor)
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
P2RY12 purinergic receptor P2Y, G-protein coupled, 12
PTGS1 prostaglandin-endoperoxide synthase 1 (prostaglandin G/H synthase and cyclooxygenase)
VKORC1 vitamin K epoxide reductase complex, subunit 1