CIM11 3B13
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Haemophilia C
- chapitre
- 03 Diseases of the blood or blood-forming organs
- bloc
- Congenital or constitutional haemorrhagic condition
- definition
- A disease caused by genetically inherited mutations. This disease is characterised by decreased levels of factor XI leading to abnormalities in coagulation of the blood. This disease may present with prolonged bleeding, easy bruising or bleeding gums. Confirmation is by identification of mutation th
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#413739466 ↗