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von Willebrand disease (hereditary or acquired)

Go to external page http://purl.obolibrary.org/obo/MONDO_0024574

Hereditary or acquired coagulation disorder characterized by a qualitative or quantitative deficiency of the von Willebrand factor. The latter plays an important role in platelet adhesion. Signs and symptoms include bruises, nose bleeding, gum bleeding following a dental procedure, heavy menstrual bleeding, and gastrointestinal bleeding. [ NCIT:C68677 ]

Synonyms: von Willebrand disorder VWD von Willebrand's disease

This is just here as a test because I lose it

Term information

database cross reference
  • SCTID:128105004 (MONDO:equivalentTo)
  • ICD9:286.4 (MONDO:i2s)
  • ICD10CM:D68.0 (MONDO:equivalentTo)
  • NCIT:C68677 (MONDO:equivalentTo)
  • NORD:1831 (MONDO:NORD)
  • MESH:D014842 (MONDO:equivalentTo)
Subsets

rare, inferred_rare

exactMatch

http://purl.bioontology.org/ontology/ICD10CM/D68.0

http://identifiers.org/mesh/D014842

http://purl.obolibrary.org/obo/NCIT_C68677

http://identifiers.org/snomedct/128105004

has related synonym

von Willebrand disease

id

MONDO:0024574

Term relations