thromboembolism Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description The formation of a blood clot inside a blood vessel that subsequently travels through the blood stream from the site where it formed to another location in the body, generally leading to vascular occlusion at the distant site. (Human Phenotype Ontology, HP_0001907)
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8 genes associated with the disease thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
CYP2C9 cytochrome P450, family 2, subfamily C, polypeptide 9
F2 coagulation factor II (thrombin)
F5 coagulation factor V (proaccelerin, labile factor)
GP1BA glycoprotein Ib (platelet), alpha polypeptide
LPA lipoprotein, Lp(a)
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
XK X-linked Kx blood group