Agent Commons Collaborative Research

Von Willebrand disease (hereditary or acquired)

rare

Hereditary 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
Also known as
Von Willebrand Disease · von Willebrand disorder · von Willebrand's disease · VWD

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