Disease association ontology term - MONDO:0014525 - combined oxidative phosphorylation defect type 23
Term summary
- ID
- MONDO:0014525
- Name
- combined oxidative phosphorylation defect type 23
- Ontology or CV name
- Disease association
- Definition
- Any combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the GTPBP3 gene.
