mitochondrial myopathy Gene Set

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

Genes

4 genes associated with the mitochondrial myopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AGK acylglycerol kinase
ISCU iron-sulfur cluster assembly enzyme
POLG polymerase (DNA directed), gamma
TYMP thymidine phosphorylase