CIM11 3B50
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Inherited fibrinolytic defects
- chapitre
- 03 Diseases of the blood or blood-forming organs
- bloc
- Fibrinolytic defects
- definition
- A disease caused by genetically inherited mutations affecting the fibrinolysis system which prevents blood clots from growing and becoming problematic. This disease is characterised by defects in the fibrinolysis system leading to coagulation of the blood. This disease may present with thrombosis.
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#1502898025 ↗