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CIM11 5C51.50

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

Hereditary fructose intolerance

chapitre
05 Endocrine, nutritional or metabolic diseases
bloc
Inborn errors of metabolism
definition
Hereditary fructose intolerance is an autosomal recessive disorder due to a deficiency of fructose-1-phosphate aldolase activity, which results in an accumulation of fructose-1-phosphate in the liver, kidney, and small intestine, and is characterised by severe abdominal pain, vomiting, and hypoglyca
exclusions
Fructose malabsorption
type
category
navigateur oms (fr)
https://icd.who.int/browse/2026-01/mms/fr#1925240365 ↗