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