|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An increase in the amount of glycogen stored in hepatocytes compared to normal. (Human Phenotype Ontology, HP_0006568)|
|Downloads & Tools|
1 genes associated with the increased hepatic glycogen content phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|PYGL||phosphorylase, glycogen, liver|