Peroxisome biogenesis disorder due to PEX14 defect
MONDO:0100268Any Zellweger spectrum disorder in which the cause of the disease is a mutation in the PEX14 gene.
Also known as: PEX14 related Zellweger spectrum disorder, peroxisome biogenesis disorder due to PEX14 defect
7 clinical trials for this condition and its sub-types, 0 tagged with Peroxisome biogenesis disorder due to PEX14 defect itself.
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Browse by category →Sub-types of Peroxisome biogenesis disorder due to PEX14 defect
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