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

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

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Sub-types

Hereditary von Willebrand disease (18) 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)

Broader categories

Disease (680) Hematologic disorder (170) Blood coagulation disease (53) Human disease (14) Coagulation protein disease (13) Disease by body system or component (0)

Trials to join now! 27 Not yet recruiting 4 Not yet finished but already full! 6 Completed 12

Von Willebrand disease (hereditary or acquired)

Sub-types

Broader categories

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