CIM11 5C51.20
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Primary hyperoxaluria type 1
- chapitre
- 05 Endocrine, nutritional or metabolic diseases
- bloc
- Inborn errors of metabolism
- definition
- Primary hyperoxaluria type 1 is a rare metabolic disorder due to a defect of the peroxysomal hepatic enzyme L-alanine: glyoxylate aminotransferase (AGT). The infantile form is characterised by chronic renal failure due to massive oxalate deposition. In other patients, urolithiasis develops with infe
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#692812009 ↗