Disease association ontology term - MONDO:0013969 - combined oxidative phosphorylation defect type 11
Term summary
- ID
- MONDO:0013969
- Name
- combined oxidative phosphorylation defect type 11
- Ontology or CV name
- Disease association
- Definition
- Any combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the RMND1 gene.
