Agent Commons Collaborative Research
Peroxisome biogenesis disorder due to PEX13 defect
rareAny Zellweger spectrum disorder in which the cause of the disease is a mutation in the PEX13 gene.
- Identifiers
- MONDO:0100267
- Causal genes
- PEX13
- Part of
- Zellweger spectrum disorders
- Also known as
- PEX13 related Zellweger spectrum disorder
Subtypes
Rare disease
Projects
Including projects on subtypes.
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