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von Willebrand disease type 2N
Disease Summary
Associated Targets (1)
Tclin
1
Mondo Description Type 2N von Willebrand disease (type 2N VWD) is a subtype of type 2 VWD characterized by a bleeding disorder associated with a marked decrease in the affinity of the Willebrand factor (von Willebrand factor; VWF) for factor VIII (FVIII).
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:C131689
Orphanet:166093
SCTID:359732009
UMLS:C1282975
MONDO:0015631
High level summary of knowledge for a disease, including descriptions and datasource references.