Von Willebrand disease 3
MONDO:0010191Type 3 von Willebrand disease (type 3 VWD) is the most severe form of VWD characterized by a bleeding disorder associated with a total or near-total absence of Willebrand factor (von Willebrand factor; VWF) in the plasma and cellular compartments, also leading to a profound deficiency of plasmatic factor VIII (FVIII).
Also known as: VWD3, von Willebrand disease 3, von Willebrand disease type 3, von Willebrand's disease 3, von Willebrand's disease type 3, VON WILLEBRAND disease, type 3, VWD, type 3, Von Willebrand disease, type 3
55 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsBroader categories
Disease
(618)
Hereditary disease
(172)
Hematologic disorder
(160)
Hemorrhagic disease
(100)
Blood coagulation disease
(51)
Von Willebrand disease (hereditary or acquired)
(37)
Hereditary von Willebrand disease
(17)
Human disease
(14)
Coagulation protein disease
(12)
Inherited blood coagulation disorder
(7)