Aide au codage
Effacer

← Retour aux résultats

CIM11 5C61.61

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

Congenital lactase deficiency

chapitre
05 Endocrine, nutritional or metabolic diseases
bloc
Disorders of metabolite absorption or transport
definition
This is a congenital deficiency of lactase (EC 3.2.1.108), inherited as an autosomal recessive trait, presenting in infancy and manifested by profuse watery diarrhoea in response to dietary milk, due to inability to digest lactose, a sugar found in milk and to a lesser extent milk-derived dairy prod
type
category
navigateur oms (fr)
https://icd.who.int/browse/2026-01/mms/fr#2109252471 ↗