All diseases

OMIM ID
261740
OMIM term:
GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL
Alternative terms:
PHOSPHORYLASE KINASE DEFICIENCY OF HEART
GLYCOGEN STORAGE DISEASE OF HEART
(∗) Location:
7q36.1  
(†) Associated OMIM genes:
PRKAG2  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/911f3513