CIM11 5C50.11

Tyrosinaemia type 1

chapitre: 05 Endocrine, nutritional or metabolic diseases
bloc: Inborn errors of metabolism
definition: Tyrosinemia type 1 is an inborn error of amino acid metabolism characterised by hepatorenal manifestations. The early-onset acute form of the disorder manifests between 15 days and 3 months after birth with hepatocellular necrosis. Septicaemia is a frequent complication. Renal tubular dysfunction oc
type: category
navigateur oms (fr): https://icd.who.int/browse/2026-01/mms/fr#2029519782 ↗