Von Willebrand disease type 2M

Orpha code: 166090OMIM code: 613554

Definicja

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.).

Disease data
Klasyfikacja

Clinical subtype

Kod ORPHA
166090
Kod OMIM
613554
Kod ICD10
D68.0
Kod ICD11
3B12

No additional description.

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