Peroxisomal Disorder

About the Disease
Peroxisomal Disease, also known as peroxisomal disorders, is related to rhizomelic chondrodysplasia punctata, type 3 and retinal dystrophy with leukodystrophy. An important gene associated with Peroxisomal Disease is PEX1 (Peroxisomal Biogenesis Factor 1), and among its related pathways/superpathways are Metabolism and Fatty acid metabolism. The drugs Betaine and Gastrointestinal Agents have been mentioned in the context of this disorder. Affiliated tissues include liver, brain and skin, and related phenotypes are no effect and no effect

Common Targets
PEX26 | PEX19 | HSD17B4 | PEX2 | PRPH2 | AMACR | PEX11B | ACOX1 | PEX16 | ACBD5 | PAX6 | PHYH | USP30 | PEX1 | PEX6 | PEX3 | ABCD1 | PEX7 | PEX10 | PEX12

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