CIM11 3A51.5
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Haemoglobin C disease
- chapitre
- 03 Diseases of the blood or blood-forming organs
- bloc
- Anaemias or other erythrocyte disorders
- definition
- A disease caused by the bi-parental gene that encodes for haemoglobin C. This disease is characterised by abnormal structure of one of the globin chains of the haemoglobin molecule. This disease may present with mild haemolytic anaemia, increased risk for gallstones, enlarged spleen, episodes of joi
- exclusions
- Hereditary persistence of fetal haemoglobin
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#2097316574 ↗