Von Willebrand disease type 2M
ORPHA:166090· ICD-10 D68.0
Definition
A subtype of type 2 von Willebrand disease characterized by a bleeding disorder associated with decreased affinity of the Willebrand factor (VWF) for platelets or collagen in the absence of any deficiency of high molecular weight VWF multimers. The disease manifests as mucocutaneous bleeding (menorrhagia, epistaxis, gastrointestinal hemorrhage, etc.).
- Prevalence
- Unknown
- Inheritance
- Autosomal dominant