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Disorder of peroxisomal beta oxidation

MONDO:0019233

Also known as: disorder of peroxisomal beta oxidation

3 clinical trials for this condition and its sub-types.

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Sub-types

Alpha-methylacyl-CoA racemase deficiency (2) D-bifunctional protein deficiency (2) Peroxisomal acyl-CoA oxidase deficiency (2) Acyl-CoA binding domain containing protein 5 deficiency (1) Sterol carrier protein 2 deficiency (1) Congenital bile acid synthesis defect 4 (0)

Broader categories

Disease (680) Metabolic disease (233) Hereditary disease (176) Inborn errors of metabolism (45) Human disease (14) Disease of genetic or genomic mechanism (2) Peroxisomal disease (2) Disease by developmental or physiological process (0) Disease by etiologic mechanism (0) Peroxisomal single enzyme/protein defect (0)

Trials to join now! 1 Not yet finished but already full! 1 Completed 1

Researchers track rare metabolic disorders to unlock secrets

Knowledge-focused Recruiting now

This study follows people with peroxisome biogenesis disorders (PBD) to learn more about how the disease progresses. Researchers will collect medical records, test results, and images over time from up to 244 participants. No new treatments are being tested; the goal is to better…

Sponsor: McGill University Health Centre/Research Institute of the McGill University Health Centre • Aim: Knowledge-focused

Last updated Jun 27, 2026 08:03 UTC