CIM11 3A50.4
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Hereditary persistence of fetal haemoglobin
- chapitre
- 03 Diseases of the blood or blood-forming organs
- bloc
- Anaemias or other erythrocyte disorders
- definition
- Hereditary persistence of fetal haemoglobin (HPFH) associated with beta-thalassaemia is a haemoglobinopathy characterised by high haemoglobin (Hb)F levels and an increased number of fetal-Hb-containing cells. The association of HPFH with beta-thalassaemia mitigates the clinical manifestations which
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#418601307 ↗