Disease association ontology term - MONDO:1060116 - FDXR-related optic atrophy mitochondrial dysfunction syndrome
Term summary
- ID
- MONDO:1060116
- Name
- FDXR-related optic atrophy mitochondrial dysfunction syndrome
- Ontology or CV name
- Disease association
- Definition
- Any mitochondrial disorder in which the cause of the disease is a mutation in the FDXR gene.
