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lethal congenital glycogen storage disease of heart

Disease Summary
Associated Targets (1)
Tchem

1


Mondo Description Any glycogen storage disease in which the cause of the disease is a mutation in the PRKAG2 gene.
Uniprot Description Rare disease which leads to death within a few weeks to a few months after birth, through heart failure and respiratory compromise.
Mondo Term and Equivalent IDs
MONDO:0009867:  lethal congenital glycogen storage disease of heart
GARD:0010728: 
MESH:C564888: 
Orphanet:439854: 
UMLS:C1849813: