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. [ http://purl.obolibrary.org/obo/ECO_0007637 url:http://ghr.nlm.nih.gov/condition/von-willebrand-disease http://purl.obolibrary.org/obo/ECO_0007638 url:http://en.wikipedia.org/wiki/Von_Willebrand_disease ]

Synonyms: von Willebrand disorder vascular pseudohemophilia von Willebrand's-Jurgens' disease vascular hemophilia von Willebrand-Jrgens disease von Willebrand disease

This is just here as a test because I lose it

Term information

database cross reference
  • ICD9CM:286.4
  • SNOMEDCT_US_2020_09_01:11093006
  • GARD:7867
  • ICD10CM:D68.0
  • MESH:D014842
  • UMLS_CUI:C0042974
  • NCI:C68677
Subsets

NCIthesaurus

comment

OMIM mapping confirmed by DO. [SN].

has obo namespace

disease_ontology

id

DOID:12531

Term relations