Hereditary von Willebrand disease

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.