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CIM11 3A51.0

CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09

Sickle cell trait

chapitre
03 Diseases of the blood or blood-forming organs
bloc
Anaemias or other erythrocyte disorders
definition
A disease caused by genetic inheritance of one abnormal allele of the haemoglobin gene. This disease does not display the severe symptoms of sickle cell disease that occurs in homozygous individuals. Confirmation is by identification of mutation through genetic testing.
type
category
navigateur oms (fr)
https://icd.who.int/browse/2026-01/mms/fr#2011497038 ↗