| 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 |