Any Zellweger spectrum disorder in which the cause of the disease is a mutation in the PEX2 gene.
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peroxisome biogenesis disorder 5A (Zellweger)
MONDO:0013932
peroxisome biogenesis disorder 5B
MONDO:0013933
peroxisome biogenesis disorder 9B
MONDO:0013945
peroxisome biogenesis disorder due to PEX1 defect
MONDO:0100259
peroxisome biogenesis disorder due to PEX3 defect
MONDO:0100261
peroxisome biogenesis disorder due to PEX5 defect
MONDO:0100262