Disease association ontology term - MONDO:0100269 - peroxisome biogenesis disorder due to PEX16 defect
Term summary
- ID
- MONDO:0100269
- Name
- peroxisome biogenesis disorder due to PEX16 defect
- Ontology or CV name
- Disease association
- Definition
- Any Zellweger spectrum disorder in which the cause of the disease is a mutation in the PEX16 gene.
