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DOID:12531 - von Willebrand's disease
Disease Ontology Definition: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.
Synonyms: vascular hemophilia, vascular pseudohemophilia, von Willebrand disease, von Willebrand disorder, von Willebrand's-Jurgens' disease, von Willebrand-Jrgens disease,
Echinobase Genes :
MIM:193400 - von willebrand disease, type 1; vwd1 |
MIM:277480 - von willebrand disease, type 3; vwd3 |
MIM:613554 - von willebrand disease, type 2; vwd2 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
inherited blood coagulation disease (is_a)