Disease association ontology term - MONDO:0014636 - combined oxidative phosphorylation defect type 25
Term summary
- ID
- MONDO:0014636
- Name
- combined oxidative phosphorylation defect type 25
- Ontology or CV name
- Disease association
- Definition
- Any combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the MARS2 gene.
