Von Willebrand disease type 2N

Orpha code: 166093OMIM code: 613554

Definicja

A subtype of type 2 von Willebrand disease characterized by a bleeding disorder associated with a marked decrease in the affinity of the Willebrand factor (VWF) for factor VIII (FVIII). Abnormal bleeding manifestations are less frequent in this VWD subtype than in other forms of the disease. The disease manifests mainly as soft tissue bleeding (haematoma, post-operative bleeding, etc.).

Disease data
Klasyfikacja

Clinical subtype

Kod ORPHA
166093
Kod OMIM
613554
Kod ICD10
D68.0
Kod ICD11
3B12

No additional description.

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