depletion of mitochondrial dna in liver Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormal reduction in the number of mitochondria in hepatocytes. (Human Phenotype Ontology, HP_0006581)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006581
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Genes

1 genes associated with the depletion of mitochondrial dna in liver phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
DGUOK deoxyguanosine kinase