Disease association ontology term - MONDO:0013986 - combined oxidative phosphorylation defect type 14
Term summary
- ID
- MONDO:0013986
- Name
- combined oxidative phosphorylation defect type 14
- Ontology or CV name
- Disease association
- Definition
- Any combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the FARS2 gene.
