Von Willebrand disease type 2N
MONDO:0015631Type 2N von Willebrand disease (type 2N VWD) is a subtype of type 2 VWD characterized by a bleeding disorder associated with a marked decrease in the affinity of the Willebrand factor (von Willebrand factor; VWF) for factor VIII (FVIII).
Also known as: von Willebrand disease Normandy variant, von Willebrand disease, type 2N
48 clinical trials for this condition and its sub-types.
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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)