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von Willebrand disease type 2M
Disease Summary
Associated Targets (1)
Tclin
1
Mondo Description Type 2M von Willebrand disease (type 2M 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 in the absence of any deficiency of high molecular weight VWF multimers.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
NCIT:C131688
Orphanet:166090
SCTID:359725000
SCTID:359729006
UMLS:C1282974
MONDO:0015630
High level summary of knowledge for a disease, including descriptions and datasource references.