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Cell Culture Ontology
| Preferred Name | von Willebrand disease type 2M | |
| Synonyms |
von Willebrand disease, type 2M |
|
| Definitions |
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 in the absence of any deficiency of high molecular weight VWF multimers. |
|
| ID |
http://purl.obolibrary.org/obo/MONDO_0015630 |
|
| database_cross_reference |
icd11.foundation:1358085002 Orphanet:166090 SCTID:359725000 MEDGEN:266186 SCTID:359729006 UMLS:C1282974 NCIT:C131688 GARD:17023
|
|
| definition |
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 in the absence of any deficiency of high molecular weight VWF multimers.
|
|
| has_exact_synonym |
von Willebrand disease, type 2M
|
|
| id |
MONDO:0015630
|
|
| in_subset |
http://purl.obolibrary.org/obo/mondo/mondo-base#rare http://purl.obolibrary.org/obo/mondo/mondo-base#otar http://purl.obolibrary.org/obo/mondo/mondo-base#ordo_subtype_of_a_disorder |
|
| label |
von Willebrand disease type 2M
|
|
| notation |
MONDO:0015630
|
|
| preferred label |
von Willebrand disease type 2M
|
|
| prefLabel |
von Willebrand disease type 2M
|
|
| skos_exactMatch |
http://identifiers.org/snomedct/359729006 http://identifiers.org/medgen/266186 http://linkedlifedata.com/resource/umls/id/C1282974 http://identifiers.org/snomedct/359725000 http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1358085002 |
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| subClassOf |
| Delete | Subject | Author | Type | Created |
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| No notes to display |