CIM11 3B10
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Hereditary factor VIII deficiency
- chapitre
- 03 Diseases of the blood or blood-forming organs
- bloc
- Congenital or constitutional haemorrhagic condition
- definition
- A disease caused by a genetically inherited mutation leading to a deficiency in clotting due to lack of factor VIII. This disease is characterised by increasing haemorrhaging and bruising. Confirmation is by identification of mutations by genetic testing.
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#1573164739 ↗