Disease association ontology term - MONDO:0014775 - combined oxidative phosphorylation deficiency 28
Term summary
- ID
- MONDO:0014775
- Name
- combined oxidative phosphorylation deficiency 28
- Ontology or CV name
- Disease association
- Definition
- Any combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the SLC25A26 gene.
