Peroxisome biogenesis disorder due to PEX12 defect

MONDO:0100266

Any Zellweger spectrum disorder in which the cause of the disease is a mutation in the PEX12 gene.

Also known as: PEX12 related Zellweger spectrum disorder, peroxisome biogenesis disorder due to PEX12 defect

7 clinical trials for this condition and its sub-types, 0 tagged with Peroxisome biogenesis disorder due to PEX12 defect itself.

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Sub-types of Peroxisome biogenesis disorder due to PEX12 defect

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