CIM11 5C51.2

Disorders of glyoxylate metabolism

chapitre: 05 Endocrine, nutritional or metabolic diseases
bloc: Inborn errors of metabolism
definition: Primary hyperoxaluria, or oxalosis, is a rare metabolic disorder transmitted as an autosomal recessive disease, including both type 1, the most frequent, and type 2, extremely rare. Hyperoxaluria type 1 is due to a defect of the peroxysomal hepatic enzyme L-alanine: glyoxylate aminotransferase (AGT)
type: category
navigateur oms (fr): https://icd.who.int/browse/2026-01/mms/fr#1800430868 ↗