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Disease Ontology Browser
von Willebrand's disease (DOID:12531)
Alliance: disease page
Synonyms: vascular hemophilia; vascular pseudohemophilia; von Willebrand disease; von Willebrand disorder; von Willebrand's-Jurgens' disease; von Willebrand-Jrgens disease
Alt IDs: OMIM:193400, OMIM:277480, OMIM:613554, ICD10CM:D68.0, ICD10CM:D69.8, ICD9CM:286.4, MESH:D014842, NCI:C68677, UMLS_CUI:C0042974
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.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
10/10/2017
MGI 6.10
The Jackson Laboratory