Glycogen Storage Disease, Type IXD Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Glycogen storage disease due to muscle phosphorylase kinase (PhK) deficiency is a benign inborn error of glycogen metabolism characterized by exercise intolerance. (Orphanet Rare Disease Ontology, Orphanet_715)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C564485
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Genes

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

Symbol Name Standardized Value
PHKA1 phosphorylase kinase, alpha 1 (muscle) 2.88009