CIM11 3A92
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Hereditary methaemoglobinaemia
- chapitre
- 03 Diseases of the blood or blood-forming organs
- bloc
- Anaemias or other erythrocyte disorders
- definition
- Hereditary methemoglobinemia (HM) is a rare red cell disorder classified principally into two clinical phenotypes: autosomal recessive congenital (or hereditary) methemoglobinemia types I and II (RCM/RHM type 1 | RCM/RHM type 2). In RCM type 1, well-tolerated cyanosis from birth is the only symptom.
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#586921197 ↗