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Von Willebrand disease (hereditary or acquired)
rareHereditary or acquired coagulation disorder characterized by a qualitative or quantitative deficiency of the von Willebrand factor. The latter plays an important role in platelet adhesion. Signs and symptoms include bruises, nose bleeding, gum bleeding following a dental procedure, heavy menstrual bleeding, and gastrointestinal bleeding.
- Identifiers
- MONDO:0024574
- Part of
- Coagulation protein disease
- Also known as
- Von Willebrand Disease · von Willebrand disorder · von Willebrand's disease · VWD
Subtypes
Disease Rare Not rare Subtypes
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