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National Cancer Institute Thesaurus
Last uploaded:
February 23, 2024
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Id | http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C68677
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C68677
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Preferred Name | von Willebrand Disease |
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.
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Synonyms |
von Willebrand Disease
von Willebrand Disorder
von Willebrand's Disease
Von Willebrand's disease
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Type | http://www.w3.org/2002/07/owl#Class |
All Properties
label |
von Willebrand Disease
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Legacy Concept Name |
von_Willebrand_Disease
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Preferred_Name |
von Willebrand Disease
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Semantic_Type |
Disease or Syndrome
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prefixIRI |
Thesaurus:C68677
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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.
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UMLS_CUI |
C0042974
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code |
C68677
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subClassOf | |
type | |
FULL_SYN |
von Willebrand Disease
von Willebrand Disorder
von Willebrand's Disease
Von Willebrand's disease
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ALT_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 mucocutaneous bleeding.
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Contributing_Source |
Cellosaurus
NICHD
mCode
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Concept_In_Subset |
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