CIM11 5C50.A2
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Argininaemia
- chapitre
- 05 Endocrine, nutritional or metabolic diseases
- bloc
- Inborn errors of metabolism
- definition
- Arginase deficiency is a rare autosomal recessive amino acid metabolism disorder characterised clinically by variable degrees of hyperammonemia, developing from about 3 years of age, and leading to progressive loss of developmental milestones and spasticity in the absence of treatment.
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#1619102598 ↗