Peroxisome biogenesis disorder due to PEX16 defect
MONDO:0100269Any Zellweger spectrum disorder in which the cause of the disease is a mutation in the PEX16 gene.
Also known as: PEX16 related Zellweger spectrum disorder, peroxisome biogenesis disorder due to PEX16 defect
7 clinical trials for this condition and its sub-types, 0 tagged with Peroxisome biogenesis disorder due to PEX16 defect itself.
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Browse by category →Sub-types of Peroxisome biogenesis disorder due to PEX16 defect
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Peroxisome biogenesis disorder 8B 0 trials