|OBO ID: DOID:12531|
|Term Name:||von Willebrand's disease||Search Ontology:|
|Definition:||A blood coagulation 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. (2)|
|Ontology:||Human Disease (DOID:12531)|
OTHER von Willebrand's disease PAGES
GENES INVOLVED No data available
PHENOTYPE No data available
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