Glycogen Storage Disease Type VI Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D006013
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Genes

1 genes/proteins associated with the disease Glycogen Storage Disease Type VI from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
PYGL phosphorylase, glycogen, liver 2.88009