CIM11 3B15
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Inherited coagulation factor deficiency without bleeding tendency
- 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 decreased levels of coagulation factor. This disease is characterised by decreased levels of coagulation factor without leading to increased haemorrhaging. Confirmation is by identification of decreased levels of coagulation factor in a
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#1795705470 ↗