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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 ↗