Medical Definition of Glycogen storage disease type VIII

1. An x-linked recessive hepatic glycogen storage disease resulting from lack of expression of phosphorylase-b-kinase activity. Symptoms are relatively mild; hepatomegaly, increased liver glycogen, and decreased leukocyte phosphorylase are present. Liver shrinkage occurs in response to glucagon. Inheritance: X-linked recessive (12 Dec 1998)

Lexicographical Neighbors of Glycogen Storage Disease Type VIII

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
glycogen storage disease type VIII (current term)
glycogen synthase
glycogen synthase-d phosphatase
glycogen synthetase
glycogenase
glycogeneses
glycogenesis
glycogenetic
glycogenic
glycogenic acanthosis
glycogenolyses
glycogenolysis
glycogenolytic
glycogenosis
glycogens

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