von willebrand disease Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A coagulation protein disease that is a hereditary abnormality which slows the blood clotting process. It arises from a qualitative or quantitative deficiency of von Willebrand factor (vWF), a multimeric protein that is required for platelet adhesion. (Human Disease Ontology, DOID_12531)
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Genes

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

Symbol Name
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)