|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Downloads & Tools|
1 genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 from the curated CTD Gene-Disease Associations dataset.
|SLC25A4||solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 4||2.88009|