Preferred Name |
von Willebrand Disease |
ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C68677 |
code |
C68677 |
Concept_In_Subset | |
Contributing_Source |
NICHD |
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. |
FULL_SYN |
von Willebrand's Disease von Willebrand Disorder |
Has_NICHD_Parent | |
label |
von Willebrand Disease |
Legacy_Concept_Name |
von_Willebrand_Disease |
NICHD_Hierarchy_Term |
von Willebrand Disease |
Preferred_Name |
von Willebrand Disease |
prefixIRI |
C68677 |
prefLabel |
von Willebrand Disease |
Semantic_Type |
Disease or Syndrome |
UMLS_CUI |
C0042974 |
subClassOf |
Delete | Mapping To | Ontology | Source |
---|---|---|---|
http://purl.bioontology.org/ontology/OMIM/MTHU016680 | Online Mendelian Inheritance in Man | LOOM |