Von Willebrand disease type 2A
MONDO:0015628Type 2A von Willebrand disease (type 2A VWD) is a subtype of type 2 VWD characterized by a bleeding disorder associated with a decrease in the affinity of the Willebrand factor (von Willebrand factor; VWF) for platelets and the subendothelium caused by a deficiency of high molecular weight VWF multimers.
Also known as: von Willebrand disease, type 2A
15 clinical trials for this condition and its sub-types.
Follow this condition to get notified about new trialsBroader categories
Disease
(717)
Hereditary disease
(188)
Hematologic disorder
(172)
Hemorrhagic disease
(107)
Blood coagulation disease
(54)
Von Willebrand disease (hereditary or acquired)
(39)
Hereditary von Willebrand disease
(18)
Human disease
(15)
Coagulation protein disease
(13)
Inherited blood coagulation disorder
(8)