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Von Willebrand disease type 2M
rareA 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.
- Identifiers
- MONDO:0015630 Orphanet:166090
- Part of
- Von Willebrand disease 2
- Also known as
- von Willebrand disease, type 2M
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