|Dataset||GAD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A myopathy that is characterized by mitochondrial dysfunction. (Human Disease Ontology, DOID_699)|
|Downloads & Tools|
1 genes associated with the disease mitochondrial myopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
|TK2||thymidine kinase 2, mitochondrial|