Any peroxisome biogenesis disorder in which the cause of the disease is a mutation in the PEX7 gene.
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rhizomelic chondrodysplasia punctata type 1
MONDO:0008972
peroxisome biogenesis disorder due to PEX5 defect in the PEX7-binding domain
MONDO:0100265
adult Refsum disease due to PEX7 defect
MONDO:0100307