Disease association ontology term - MONDO:0859321 - mitochondrial complex III deficiency, nuclear type 11
Term summary
- ID
- MONDO:0859321
- Name
- mitochondrial complex III deficiency, nuclear type 11
- Ontology or CV name
- Disease association
- Definition
- Any mitochondrial complex III deficiency in which the cause of the disease is a mutation in the UQCRH gene.
