peroxisome biogenesis disorder due to PEX19 defect
MONDO:0100270Mondo
Findings
No curated finding names peroxisome biogenesis disorder due to PEX19 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 PEX19 gene.
Definition from the Mondo Disease Ontology (MONDO:0100270), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
- Narrower terms (1)
Other names
1 name
Resolves to: peroxisome biogenesis disorder due to PEX19 defect
- Also called
- PEX19 related Zellweger spectrum disorder