Peroxisome biogenesis disorder due to PEX5 defect in the PEX7-binding domain

MONDO:0100265

Any peroxisome biogenesis disorder due to PEX5 in which the cause of the disease is a mutation in the PEX7-binding domain of the PEX5 gene.

Also known as: peroxisome biogenesis disorder due to PEX5 defect in the PEX7-binding domain

8 clinical trials for this condition and its sub-types, 0 tagged with Peroxisome biogenesis disorder due to PEX5 defect in the PEX7-binding domain itself.

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↑ Syndromic dyslipidemia (73) ↑ Rhizomelic chondrodysplasia punctata (2) ↑ Non-Zellweger spectrum disorder (1)

Sub-types of Peroxisome biogenesis disorder due to PEX5 defect in the PEX7-binding domain

Rhizomelic chondrodysplasia punctata type 5 1 trial

Including sub-types (8) Tagged with Peroxisome biogenesis disorder due to PEX5 defect in the PEX7-binding domain (0)

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