Human genes for von Willebrand's disease
Von Willebrand's disease [DOID:12531]
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.
Synonyms: von Willebrand's disease, DOID:12531, von Willebrands disease, von Willebrand's disorder, von Willebrand's syndrome ...