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)
Downloads & Tools
1 genes involed in the disease von willebrand's disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.