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Von Willebrand disease type 2N
Disease 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.).
ORPHA:166093
Classification level: Subtype of disorder- Synonym(s): -
- Prevalence: Unknown
- Inheritance: Autosomal recessive
- Age of onset: -
- ICD-10: D68.0
- OMIM: 613554
- UMLS: C1282975
- MeSH: -
- GARD: -
- MedDRA: -
Detailed information
Article for general public
Professionals
- Emergency guidelines
- Français (2019, pdf)
- Anesthesia guidelines
- English (2014, pdf)
- Czech (2014, pdf)
- Español (2014, pdf)
- Clinical genetics review
- English (2017)
Additional information
Further information on this disease
Health care resources for this disease
Research activities on this disease
Specialised Social Services
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