|Dataset||GAD Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
4 genes associated with the disease von willebrand disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.