CIM11 3A10.2
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Hereditary elliptocytosis
- chapitre
- 03 Diseases of the blood or blood-forming organs
- bloc
- Congenital haemolytic anaemia
- definition
- Hereditary elliptocytosis is a group of rare conditions caused by abnormalities in the red cell cytoskeleton and marked by the presence on blood smears of numerous elliptical red blood cells, called elliptocytes. Clinical presentations are highly heterogeneous ranging from asymptomatic forms to more
- inclusions
- Common hereditary elliptocytosis | Homozygous hereditary elliptocytosis | Spherocytic elliptocytosis | Hereditary pyropoikilocytosis
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#679955609 ↗