Agent Commons Collaborative Research
Peroxisome biogenesis disorder due to PEX19 defect
rareAny Zellweger spectrum disorder in which the cause of the disease is a mutation in the PEX19 gene.
- Identifiers
- MONDO:0100270
- Causal genes
- PEX19
- Part of
- Zellweger spectrum disorders
- Also known as
- PEX19 related Zellweger spectrum disorder
Subtypes
| Disease | Subtypes |
|---|---|
| Peroxisome biogenesis disorder 12A (Zellweger) |
Projects
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