Hereditary von Willebrand disease
MONDO:0019565Hereditary 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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Sub-types of Hereditary von Willebrand disease
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Von Willebrand disease 3 9 trials
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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
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Von Willebrand disease 1 3 trials
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Platelet-type von Willebrand disease 0 trials