loading...| Preferred Name |
von Willebrand Disease |
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| Synonyms |
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| 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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| ID |
http://purl.obolibrary.org/obo/NCIT_C68677 |
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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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| code |
C68677 |
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| Contributing_Source |
Cellosaurus NICHD |
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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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| in_subset |
http://purl.obolibrary.org/obo/NCIT_C90259 http://purl.obolibrary.org/obo/NCIT_C132009 |
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| 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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| prefixIRI |
NCIT:C68677 |
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| prefLabel |
von Willebrand Disease |
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| Semantic_Type |
Disease or Syndrome |
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| UMLS_CUI |
C0042974 |
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| subClassOf |