glycogen storage disease type i Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A glycogen storage disease that has_material_basis_in deficiency of the glucose-6-phosphatase enzyme which impairs the ability of the liver to produce free glucose from glycogen and from gluconeogenesis and is characterized by accumulation of glycogen and fat in the liver and kidneys, resulting in hepatomegaly and renomegaly. (Human Disease Ontology, DOID_2749)
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Genes

1 genes associated with the disease glycogen storage disease type i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
G6PC glucose-6-phosphatase, catalytic subunit