CIM11 3B50.1
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Congenital plasminogen activator inhibitor type 1 deficiency
- chapitre
- 03 Diseases of the blood or blood-forming organs
- bloc
- Fibrinolytic defects
- definition
- Congenital plasminogen activator inhibitor type 1 (PAI-1) deficiency is a disorder that causes premature lysis of haemostatic clots and a moderate bleeding syndrome. Spontaneous bleeding is rarely observed, whereas moderate haemorrhages of the knees, elbows, nose and gingiva are usually triggered by
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#428643962 ↗