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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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