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Experimental Factor Ontology
Preferred Name | von Willebrand disease type 2A | |
Synonyms |
von Willebrand disease, type 2A |
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Definitions |
Type 2A von Willebrand disease (type 2A VWD) is a subtype of type 2 VWD characterized by a bleeding disorder associated with a decrease in the affinity of the Willebrand factor (von Willebrand factor; VWF) for platelets and the subendothelium caused by a deficiency of high molecular weight VWF multimers. |
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ID |
http://purl.obolibrary.org/obo/MONDO_0015628 |
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database_cross_reference |
MEDGEN:220920 SCTID:359714009 Orphanet:166084 icd11.foundation:1009291548 UMLS:C1282968 NCIT:C131686 GARD:17021
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definition |
Type 2A von Willebrand disease (type 2A VWD) is a subtype of type 2 VWD characterized by a bleeding disorder associated with a decrease in the affinity of the Willebrand factor (von Willebrand factor; VWF) for platelets and the subendothelium caused by a deficiency of high molecular weight VWF multimers.
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exactMatch |
http://identifiers.org/medgen/220920 http://www.orpha.net/ORDO/Orphanet_166084 http://linkedlifedata.com/resource/umls/id/C1282968 http://identifiers.org/snomedct/359714009 http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1009291548 |
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has_exact_synonym |
von Willebrand disease, type 2A
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id |
MONDO:0015628
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in_subset |
http://purl.obolibrary.org/obo/mondo#rare http://purl.obolibrary.org/obo/mondo#nord_rare http://purl.obolibrary.org/obo/mondo#otar http://purl.obolibrary.org/obo/mondo#gard_rare http://purl.obolibrary.org/obo/mondo#ordo_subtype_of_a_disorder |
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label |
von Willebrand disease type 2A
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notation |
MONDO:0015628
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preferred label |
von Willebrand disease type 2A
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prefLabel |
von Willebrand disease type 2A
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subClassOf |
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