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Peroxisome biogenesis disorder due to PEX11B defect

MONDO:0100279

Any peroxisome biogenesis disorder in which the cause of the disease is a mutation in the PEX11B gene.

Also known as: PEX11B related peroxisome biogenesis disorder, peroxisome biogenesis disorder due to PEX11B defect

7 clinical trials for this condition and its sub-types, 0 tagged with Peroxisome biogenesis disorder due to PEX11B defect itself.

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↑ Zellweger spectrum disorders (7)

Sub-types of Peroxisome biogenesis disorder due to PEX11B defect

Including sub-types (7) Tagged with Peroxisome biogenesis disorder due to PEX11B defect (0)
Trials to join now! 4 Completed 2 Terminated 1
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