1.13.a

Disorders of glyoxylate and oxalate metabolism

  • Glyoxylate reductase/hydroxypyruvate reductase deficiency (Primary hyperoxaluria type 2)
  • Hydroxyacid oxidase 1 deficiency (Glycolate oxidase deficiency; isolated glycolic aciduria)
  • Alanine-glyoxylate aminotransferase deficiency (Primary hyperoxaluria type 1)
  • Oxalate transporter deficiency

Subnetworks

cfao 1

C-FAO

Carbohydrate, fatty acid oxidation and ketone bodies disorders

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