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Disorder of defective peroxisome oxidative status

MONDO:0100306

Any peroxisomal single enzyme/protein defect that has its basis in the disruption of peroxisome oxidation.

Also known as: disorder of defective peroxisome oxidative status

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

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Sub-types

Mitchell syndrome (1) Acatalasia (0) Mulibrey nanism (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 Completed 1
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  • New diagnostic strategy aims to end diagnostic odyssey for rare diseases

    Diagnosis Completed

    This study tested a new approach to diagnose peroxisomal disorders, a group of rare genetic diseases. The strategy uses advanced metabolic and genetic tests to find the cause faster in people with suspicious symptoms or lab results. Researchers included 8 participants from four h…

    Sponsor: University Hospital, Lille • Aim: Diagnosis

    Last updated Jun 27, 2026 08:02 UTC

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