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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9 genes associated with the von Willebrand Disease phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.