loading...| Preferred Name |
von Willebrand Disease |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C68677 |
| 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. |
| code |
C68677 |
| Concept_In_Subset |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C193006 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C193181 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C192842 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C165258 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C90259 |
| Contributing_Source |
NICHD mCode Cellosaurus |
| 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 Disease von Willebrand's Disease Von Willebrand's disease von Willebrand Disorder |
| label |
von Willebrand Disease |
| Legacy Concept Name |
von_Willebrand_Disease |
| Preferred_Name |
von Willebrand Disease |
| prefixIRI |
Thesaurus:C68677 |
| prefLabel |
von Willebrand Disease |
| Semantic_Type |
Disease or Syndrome |
| UMLS_CUI |
C0042974 |
| subClassOf |