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DOID:12531 - von Willebrand's disease
Disease 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.
Synonyms: vascular hemophilia, vascular pseudohemophilia, von Willebrand disease, von Willebrand disorder, von Willebrand-Jrgens disease, von Willebrand's-Jurgens' disease
Xenbase Genes
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vwf
| MONDO:0019565 - hereditary von Willebrand disease |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
blood coagulation disease (is_a)