|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An abnormal reduction in the number of mitochondria in hepatocytes. (Human Phenotype Ontology, HP_0006581)|
|Downloads & Tools|
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.