Hereditary von Willebrand disease

MONDO:0019565

Hereditary von Willebrand disease (VWD) is a hereditary bleeding disorder caused by a genetic anomaly leading to quantitative, structural or functional abnormalities of the Willebrand factor (von Willebrand factor; VWF). Two major groups of VWF deficiency have been defined: quantitative and partial (type 1) or total (type 3), and qualitative (type 2) with several subtypes (2A, 2B, 2M, 2N).

Also known as: vascular haemophilia, vascular hemophilia, von Willebrand disease, von Willebrand disorder, von Willebrand's-Jurgens' disease, von Willebrand-Jurgens disease, congenital von willebrand's disease, hereditary von Willebrand disease

40 clinical trials for this condition and its sub-types, 18 tagged with Hereditary von Willebrand disease itself.

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Where it sits in the disease tree

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Part of

↑ Hemorrhagic disease (510) ↑ Inherited blood coagulation disorder (323) ↑ Von Willebrand disease (hereditary or acquired) (46)

Sub-types of Hereditary von Willebrand disease

Von Willebrand disease 3 9 trials
Von Willebrand disease 2 4 trials · 5 incl. sub-types
4 sub-types
- Von Willebrand disease type 2A 2 trials
- Von Willebrand disease type 2N 2 trials
- Von Willebrand disease type 2B 1 trial
- Von Willebrand disease type 2M 1 trial
Von Willebrand disease 1 3 trials
Von Willebrand disease, X-linked form 0 trials
Platelet-type von Willebrand disease 0 trials

Including sub-types (40) Tagged with Hereditary von Willebrand disease (18)

Trials to join now! 21 Not yet recruiting 2 Not yet finished but already full! 5 Completed 12

Hereditary von Willebrand disease

Where it sits in the disease tree

Ginger vs. heavy periods: a natural approach for women with bleeding disorders

Scientists hunt for hidden triggers of dangerous blood clots