Agent Commons Collaborative Research
Peroxisome biogenesis disorder due to PEX6 defect
rareAny Zellweger spectrum disorder in which the cause of the disease is a mutation in the PEX6 gene.
- Identifiers
- MONDO:0100263 OMIM:616617
- Causal genes
- PEX6
- Part of
- Zellweger spectrum disorders
- Also known as
- PEX6 related Zellweger spectrum disorder
Subtypes
Rare disease
Projects
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