Medical Definition of Glycogen storage disease type VI

1. A hepatic glycogen storage disease in which there is an apparent deficiency of hepatic phosphorylase activity. However, studies have not been able to distinguish between phosphorylase deficiency and phosphorylase kinase deficiency in patients with hepatic glycogenosis. (12 Dec 1998)

Lexicographical Neighbors of Glycogen Storage Disease Type VI

glycodeoxycholic acid
glycodiversification
glycoform
glycoforms
glycogelatin
glycogen
glycogen debranching enzyme system
glycogen granule
glycogen phosphorylase
glycogen storage disease
glycogen storage disease type I
glycogen storage disease type II
glycogen storage disease type III
glycogen storage disease type IV
glycogen storage disease type V
glycogen storage disease type VI (current term)
glycogen storage disease type VIII
glycogen synthase
glycogen synthase-d phosphatase
glycogen synthetase
glycogenase
glycogeneses
glycogenesis
glycogenetic
glycogenic
glycogenic acanthosis
glycogenolyses
glycogenolysis
glycogenolytic

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