Any Zellweger spectrum disorder in which the cause of the disease is a mutation in the PEX16 gene.
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peroxisome biogenesis disorder 8A (Zellweger)
MONDO:0013942
peroxisome biogenesis disorder 8B
MONDO:0013943
peroxisome biogenesis disorder 9B
MONDO:0013945
peroxisome biogenesis disorder due to PEX1 defect
MONDO:0100259
peroxisome biogenesis disorder due to PEX2 defect
MONDO:0100260
peroxisome biogenesis disorder due to PEX3 defect
MONDO:0100261