CIM11 3A51.9

Haemoglobin O 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 inheritance of the gene that encodes for haemoglobin O. 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 sple
type: category
navigateur oms (fr): https://icd.who.int/browse/2026-01/mms/fr#1439043542 ↗