von willebrand's disease Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
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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Genes

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

Symbol Name
VWF von Willebrand factor
Funding