CIM11 3A10.3
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Familial pseudohyperkalaemia
- chapitre
- 03 Diseases of the blood or blood-forming organs
- bloc
- Congenital haemolytic anaemia
- definition
- A disease caused by a genetically inherited mutation. This disease is characterised by a temperature-dependent defect in red cell membrane permeability to potassium that leads to high in vitro potassium levels in samples stored below 37°C leading to elevated potassium levels in the blood that does n
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#1653996588 ↗