Von Willebrand disease type 2B

Orpha code: 166087OMIM code: 613554

Definicja

A subtype of type 2 von Willebrand disease characterized by a bleeding disorder associated with increased affinity of the Willebrand factor (VWF) for platelets leading to rapid clearance of both the platelets (increasing the risk of thrombocytopenia) and VWF from the plasma. The disease manifests as mucocutaneous bleeding (menorrhagia, epistaxis, gastrointestinal hemorrhage, etc.).

Disease data
Klasyfikacja

Clinical subtype

Kod ORPHA
166087
Kod OMIM
613554
Kod ICD10
D68.0
Kod ICD11
3B12

No additional description.

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