Any peroxisome biogenesis disorder due to PEX5 in which the cause of the disease is a mutation in the PEX7-binding domain of the PEX5 gene.
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familial apolipoprotein C-II deficiency
MONDO:0008810
sitosterolemia
MONDO:0008863
cerebrotendinous xanthomatosis
MONDO:0008948
rhizomelic chondrodysplasia punctata type 1
MONDO:0008972
apparent mineralocorticoid excess
MONDO:0009025
rhizomelic chondrodysplasia punctata type 2
MONDO:0009112