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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

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

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Sub-types

Von Willebrand disease 3 (9) Von Willebrand disease 2 (4) 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 (618) Hereditary disease (172) Hematologic disorder (160) Hemorrhagic disease (100) Blood coagulation disease (51) Von Willebrand disease (hereditary or acquired) (37) Human disease (14) Coagulation protein disease (12) Inherited blood coagulation disorder (7) Disease of genetic or genomic mechanism (2)
Trials to join now! 35 Not yet recruiting 4 Not yet finished but already full! 8 Completed 23 Terminated 1
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