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Pediatric Terminology
Last uploaded:
January 25, 2013
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Preferred Name | Von_Willebrand_Disorder | |
Synonyms |
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ID |
http://www.owl-ontologies.com/Ontology1358660052.owl#Von_Willebrand_Disorder |
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ID |
C68677
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NCI_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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NCI_PT |
von Willebrand Disease
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NICHD_Definition |
_
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prefixIRI |
Von_Willebrand_Disorder
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prefLabel |
Von_Willebrand_Disorder
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Subset_Association1 |
NICHD Pediatric Terminology
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Subset_Association2 |
Neonatal Research Network Terminology
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SYN | ||
subClassOf |
http://www.owl-ontologies.com/Ontology1358660052.owl#Coagulation_Factor_Deficiency_Syndrome |
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Mapping To | Ontology | Source |
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http://purl.bioontology.org/ontology/SNOMEDCT/128105004 | SNOMEDCT | LOOM |