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)
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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