| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A myopathy that is characterized by mitochondrial dysfunction. (Human Disease Ontology, DOID_699) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0003737 |
| Similar Terms | |
| Downloads & Tools |
4 genes associated with the mitochondrial myopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
