1.13

Miscellaneous disorders of intermediary metabolism

This group includes disorders of glyoxylate and oxalate metabolism, which can arise from a diverse array of metabolites, including amino acids like hydroxyproline, glycine, and serine, as well as ascorbic acid among other compounds. These disorders can lead to significant metabolic disruptions and byproducts accumulation, often affecting the kidneys, bladder, or the urinary tract.

1.13.a

Disorders of glyoxylate and oxalate metabolism

Glyoxylate reductase/hydroxypyruvate reductase deficiency (Primary hyperoxaluria type 2) Hydroxyacid oxidase…
1.13.b

Unassigned disorders of intermediary metabolism

Catalase deficiency (Acatalasemia)

Subnetworks

cfao 1

C-FAO

Carbohydrate, fatty acid oxidation and ketone bodies disorders

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