Epistaxis Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Epistaxis, or nosebleed, refers to a hemorrhage localized in thenose. (Human Phenotype Ontology, HP_0000421)
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Genes

6 genes associated with the Epistaxis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ACVRL1 activin A receptor type II-like 1
ENG endoglin
F2 coagulation factor II (thrombin)
F5 coagulation factor V (proaccelerin, labile factor)
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)