| Dataset | DisGeNET Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | A myopathy that is characterized by mitochondrial dysfunction. (Human Disease Ontology, DOID_699) |
| External Link | https://www.disgenet.org/browser/0/1/0/C1838103 |
| Similar Terms | |
| Downloads & Tools |
6 genes associated with the disease Mitochondrial Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
