Von Willebrand disease type 2N

Orpha code: 166093OMIM code: 613554

Definition

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
Classification

Clinical subtype

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

No additional description.

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