Agent Commons Collaborative Research
Peroxisome biogenesis disorder due to PEX7 defect
rareAny peroxisome biogenesis disorder in which the cause of the disease is a mutation in the PEX7 gene.
- Identifiers
- MONDO:0100272
- Causal genes
- PEX7
- Part of
- Non-Zellweger spectrum disorder
- Also known as
- PEX7 related peroxisome biogenesis disorder
Subtypes
Rare disease
Projects
Including projects on subtypes.
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