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Up to: Hemorrhagic disease · Inherited blood coagulation disorder · Von Willebrand disease (hereditary or acquired)
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).
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Von Willebrand disease 3 9 trials
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Von Willebrand disease 2 4 trials · 5 incl. sub-types Sub-types →
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Von Willebrand disease 1 3 trials
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Platelet-type von Willebrand disease 0 trials