CIM11 3B14.1
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Hereditary factor X deficiency
- chapitre
- 03 Diseases of the blood or blood-forming organs
- bloc
- Congenital or constitutional haemorrhagic condition
- definition
- Congenital factor X deficiency is an inherited bleeding disorder with a decreased antigen and/or activity of factor X (FX) and characterised by mild to severe bleeding symptoms.
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#1886781445 ↗