Von Willebrand disease (hereditary or acquired)

MONDO:0024574

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.

Also known as: VWD, Von Willebrand Disease, von Willebrand disorder, von Willebrand's disease, von Willebrand disease

80 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Sub-types

Broader categories

Sort by