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Up to: Peroxisomal disease
Peroxisomal single enzyme/protein defect
Any peroxisomal disease in which the cause of the disease is a defect in a single enyme or protein.
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Disorder of peroxisomal transporter 0 trials · 21 incl. sub-types Sub-types →
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Disorder of glyoxylate metabolism 0 trials · 10 incl. sub-types Sub-types →
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Disorder of peroxisomal alpha oxidation 0 trials · 4 incl. sub-types Sub-types →
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Disorder of peroxisomal beta oxidation 0 trials · 2 incl. sub-types Sub-types →
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Disorder of plasmalogens biosynthesis 0 trials · 2 incl. sub-types Sub-types →
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Disorder of defective peroxisome oxidative status 0 trials · 1 incl. sub-types Sub-types →