Von Willebrand disease type 2M
MONDO:0015630A 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 in the absence of any deficiency of high molecular weight VWF multimers.
Also known as: von Willebrand disease, type 2M
14 clinical trials for this condition and its sub-types.
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Disease
(680)
Hereditary disease
(176)
Hematologic disorder
(170)
Hemorrhagic disease
(103)
Blood coagulation disease
(53)
Von Willebrand disease (hereditary or acquired)
(39)
Hereditary von Willebrand disease
(18)
Human disease
(14)
Coagulation protein disease
(13)
Inherited blood coagulation disorder
(8)