Disease association ontology term - MONDO:0012238 - progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2
Term summary
- ID
- MONDO:0012238
- Name
- progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2
- Ontology or CV name
- Disease association
- Definition
- Any progressive external ophthalmoplegia with mitochondrial DNA deletions in which the cause of the disease is a mutation in the SLC25A4 gene.
