Cell Culture Ontology

Last uploaded: July 23, 2014
Preferred Name

von Willebrand disease (hereditary or acquired)
Synonyms

von Willebrand disease

von Willebrand's disease

Von Willebrand Disease

von Willebrand disorder

VWD

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

MESH:D014842

MEDGEN:22686

NANDO:2200682

SCTID:128105004

UMLS:C0042974

NCIT:C68677

ICD10CM:D68.0

ICD9:286.4

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

Von Willebrand Disease

von Willebrand disorder

VWD

has_related_synonym

von Willebrand disease

id

MONDO:0024574

in_subset

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

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

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

label

von Willebrand disease (hereditary or acquired)

notation

MONDO:0024574

preferred label

von Willebrand disease (hereditary or acquired)

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

subClassOf

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

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