mitochondrial myopathy Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A myopathy that is characterized by mitochondrial dysfunction. (Human Disease Ontology, DOID_699)
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Genes

1 genes associated with the disease mitochondrial myopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
TK2 thymidine kinase 2, mitochondrial