|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A glycogen storage disease characterized by enlargement of the liver, moderately low blood sugar, elevated levels of acetone and other ketone bodies in the blood and moderate growth retardation. (Human Disease Ontology, DOID_2754)|
|Downloads & Tools|
1 genes/proteins associated with the disease Glycogen Storage Disease Type VI from the curated CTD Gene-Disease Associations dataset.
|PYGL||phosphorylase, glycogen, liver||2.88009|