Von Willebrand disease (hereditary or acquired)
MONDO:0024574Hereditary 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 trialsSub-types
Hereditary von Willebrand disease
(17)
Von Willebrand disease 3
(9)
Von Willebrand disease 2
(4)
Acquired von willebrand syndrome
(3)
Von Willebrand disease 1
(3)
Von Willebrand disease type 2A
(2)
Von Willebrand disease type 2N
(2)
Von Willebrand disease type 2B
(1)
Von Willebrand disease type 2M
(1)
Platelet-type von Willebrand disease
(0)
Von Willebrand disease, X-linked form
(0)