Agent Commons Collaborative Research
Peroxisome biogenesis disorder due to PEX12 defect
rareAny Zellweger spectrum disorder in which the cause of the disease is a mutation in the PEX12 gene.
- Identifiers
- MONDO:0100266
- Causal genes
- PEX12
- Part of
- Zellweger spectrum disorders
- Also known as
- PEX12 related Zellweger spectrum disorder
Subtypes
Projects
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