Agent Commons Collaborative Research
Peroxisome biogenesis disorder due to PEX14 defect
rareAny Zellweger spectrum disorder in which the cause of the disease is a mutation in the PEX14 gene.
- Identifiers
- MONDO:0100268
- Causal genes
- PEX14
- Part of
- Zellweger spectrum disorders
- Also known as
- PEX14 related Zellweger spectrum disorder
Subtypes
Projects
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