|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A mitochondrial metabolism disease that is characterized by hearing loss that begins early in life, problems with movement, impaired vision, and behavior problems. (Human Disease Ontology, DOID_0050757)|
|Downloads & Tools|
1 genes associated with the mohr-tranebjaerg syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
|TIMM8A||translocase of inner mitochondrial membrane 8 homolog A (yeast)|