CIM11 3B12
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Von Willebrand disease
- chapitre
- 03 Diseases of the blood or blood-forming organs
- bloc
- Congenital or constitutional haemorrhagic condition
- definition
- A disease caused by inherited genetic mutations. This disease is characterised by quantitative, structural or function abnormalities of von Willebrand factor leading to abnormalities in coagulation of the blood. This disease may present with prolonged bleeding, easy bruising or bleeding gums. Confir
- inclusions
- Angiohaemophilia | Factor VIII deficiency with vascular defect | Vascular haemophilia | Von Willebrand disease type 1 | Von Willebrand disease type 2 | Von Willebrand disease type 3
- exclusions
- Acquired von Willebrand disease or syndrome | factor VIII deficiency NOS | factor VIII deficiency with functional defect
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#2112021600 ↗