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glycogen storage disease IXc

Disease Summary
Associated Targets (2)
Tchem

1

Tbio

1


Mondo Description A liver PhK deficiency caused by variants in the PHKG2 gene
Uniprot Description A metabolic disorder manifesting in infancy with hepatomegaly, growth retardation, hypotonia, liver dysfunction, and elevated plasma aminotransferases and lipids. These symptoms improve with age in most cases; however, some patients may develop hepatic fibrosis or cirrhosis.
Mondo Term and Equivalent IDs
MONDO:0013091:  glycogen storage disease IXc
MESH:C567809: 
UMLS:C2751643: