glycogen storage disease vi Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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://www.omim.org/entry/232700
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Genes

1 genes associated with the glycogen storage disease vi phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
PYGL phosphorylase, glycogen, liver