Mondo Disease Ontology

Last uploaded: January 7, 2025
Preferred Name

von Willebrand disease (hereditary or acquired)
Synonyms

von Willebrand disease

von Willebrand's disease

VWD

Von Willebrand Disease

von Willebrand disorder

Definitions

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.

ID

http://purl.obolibrary.org/obo/MONDO_0024574

database_cross_reference

MEDGEN:22686

MESH:D014842

NCIT:C68677

NANDO:2200682

ICD9:286.4

SCTID:128105004

UMLS:C0042974

ICD10CM:D68.0

definition

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.

has_exact_synonym

von Willebrand's disease

VWD

Von Willebrand Disease

von Willebrand disorder

has_related_synonym

von Willebrand disease

id

MONDO:0024574

in_subset

http://purl.obolibrary.org/obo/mondo/mondo-simple#otar

http://purl.obolibrary.org/obo/mondo/mondo-simple#rare

http://purl.obolibrary.org/obo/mondo/mondo-simple#gard_rare

label

von Willebrand disease (hereditary or acquired)

notation

MONDO:0024574

prefLabel

von Willebrand disease (hereditary or acquired)

skos_exactMatch

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

http://identifiers.org/mesh/D014842

http://linkedlifedata.com/resource/umls/id/C0042974

http://identifiers.org/medgen/22686

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

http://identifiers.org/snomedct/128105004

treeView

http://purl.obolibrary.org/obo/MONDO_0002242

subClassOf

http://purl.obolibrary.org/obo/MONDO_0002242

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