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, 39 tagged with Von Willebrand disease (hereditary or acquired) itself.

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Where it sits in the disease tree

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Part of

↑ Coagulation protein disease (274)

Sub-types of Von Willebrand disease (hereditary or acquired)

Hereditary von Willebrand disease 18 trials · 29 incl. sub-types
5 sub-types
- Von Willebrand disease 3 9 trials
- Von Willebrand disease 2 4 trials · 5 incl. sub-types Sub-types →
- Von Willebrand disease 1 3 trials
- Von Willebrand disease, X-linked form 0 trials
- Platelet-type von Willebrand disease 0 trials
Acquired von willebrand syndrome 3 trials

Most studied deeper sub-types

Von Willebrand disease type 2A (2) Von Willebrand disease type 2N (2) Von Willebrand disease type 2B (1) Von Willebrand disease type 2M (1)

Including sub-types (49) Tagged with Von Willebrand disease (hereditary or acquired) (39)

Trials to join now! 23 Not yet recruiting 2 Not yet finished but already full! 3 Completed 11

Von Willebrand disease (hereditary or acquired)

Where it sits in the disease tree

Most studied deeper sub-types

New study aims to uncover hidden bleeding disorder in egyptian kids

Scientists hunt for hidden triggers of dangerous blood clots