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Peroxisome biogenesis disorder due to PEX7 defect

MONDO:0100272

Any peroxisome biogenesis disorder in which the cause of the disease is a mutation in the PEX7 gene.

Also known as: PEX7 related peroxisome biogenesis disorder, adult refsum disease due to PEX7 defect (formerly), rhizomelic chondrodysplasia punctata type 1 (formerly)

8 clinical trials for this condition and its sub-types, 0 tagged with Peroxisome biogenesis disorder due to PEX7 defect itself.

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Sub-types of Peroxisome biogenesis disorder due to PEX7 defect

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