OBO ID: DOID:12531
Term Name: von Willebrand's disease Search Ontology:
  • vascular hemophilia
  • vascular pseudohemophilia
  • von Willebrand disease
  • von Willebrand disorder
  • von Willebrand's-Jurgens' disease
  • von Willebrand-Jrgens disease
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. (2)
  • GARD:7867
  • ICD10CM:D68.0
  • ICD9CM:286.4
  • MESH:D014842
  • NCI:C68677
  • SNOMEDCT_US_2020_09_01:11093006
  • UMLS_CUI:C0042974
Ontology: Human Disease   (DOID:12531)
OTHER von Willebrand's disease PAGES
GENES INVOLVED No data available
PHENOTYPE No data available