Disorder of peroxisomal alpha oxidation
MONDO:0100277Any peroxisomal single enzyme/protein defect that has its basis in the disruption of peroxisomal alpha oxidatiion.
Also known as: disorder of peroxisomal alpha oxidation
5 clinical trials for this condition and its sub-types, 0 tagged with Disorder of peroxisomal alpha oxidation itself.
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Browse by category →Sub-types of Disorder of peroxisomal alpha oxidation
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Phytanoyl-CoA hydroxylase deficiency 0 trials · 4 incl. sub-types
1 sub-type
- Adult Refsum disease 4 trials
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