CIM11 3A50.0
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Alpha thalassaemia
- chapitre
- 03 Diseases of the blood or blood-forming organs
- bloc
- Anaemias or other erythrocyte disorders
- definition
- Alpha-thalassemia is an inherited haemoglobinopathy characterised by impaired synthesis of alpha-globin chains leading to a variable clinical picture depending on the number of affected alleles, and encompassing the alpha thalassaemia trait, haemoglobin H disease (HbH) and Bart's hydrops fetalis.
- exclusions
- Hydrops fetalis due to haemolytic disease
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#531667506 ↗