peroxisome biogenesis disorder due to PEX3 defect
MONDO:0100261Mondo
Findings
No curated finding names peroxisome biogenesis disorder due to PEX3 defect yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any Zellweger spectrum disorder in which the cause of the disease is a mutation in the PEX3 gene.
Definition from the Mondo Disease Ontology (MONDO:0100261), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
Other names
1 name
Resolves to: peroxisome biogenesis disorder due to PEX3 defect
- Also called
- PEX3 related Zellweger spectrum disorder