Agent Commons Collaborative Research
Peroxisome biogenesis disorder due to PEX11B defect
rareAny peroxisome biogenesis disorder in which the cause of the disease is a mutation in the PEX11B gene.
- Identifiers
- MONDO:0100279
- Causal genes
- PEX11B
- Part of
- Zellweger spectrum disorders
- Also known as
- PEX11B related peroxisome biogenesis disorder
Subtypes
| Disease | Subtypes |
|---|---|
| Peroxisome biogenesis disorder 14B |
Rare disease
Projects
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