CIM11 5C51.40
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Galactose-1-phosphate uridyltransferase deficiency
- chapitre
- 05 Endocrine, nutritional or metabolic diseases
- bloc
- Inborn errors of metabolism
- definition
- Classic galactosemia is a life-threatening metabolic disease with onset in the neonatal period. Infants usually develop feeding difficulties, lethargy, and severe liver disease.
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#2011000259 ↗