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von Willebrand's disease

Go to external page http://purl.obolibrary.org/obo/DOID_12531

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_0007638 url:http://en.wikipedia.org/wiki/Von_Willebrand_disease http://purl.obolibrary.org/obo/ECO_0007637 url:http://ghr.nlm.nih.gov/condition/von-willebrand-disease ]

Synonyms: vascular pseudohemophilia von Willebrand disorder 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
  • ICD10CM:D68.0
  • GARD:7867
  • ICD9CM:286.4
  • UMLS_CUI:C0042974
  • SNOMEDCT_US_2023_03_01:11093006
  • MESH:D014842
  • NCI:C68677
Subsets

DO_rare_slim, NCIthesaurus

comment

OMIM mapping confirmed by DO. [SN].

has obo namespace

disease_ontology

id

DOID:12531

Term relations