Disease association ontology term - MONDO:0014269 - combined oxidative phosphorylation deficiency 19
Term summary
- ID
- MONDO:0014269
- Name
- combined oxidative phosphorylation deficiency 19
- Ontology or CV name
- Disease association
- Definition
- Any combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the LYRM4 gene.
