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Glycogen storage disease type VIII (medical condition): A mild glycogen storage disease which affects males only and involves a...more »
See also:
Glycogenosis type 8:
»Introduction: Glycogenosis type 8
»Symptoms of Glycogenosis type 8
Glycogen storage disease type VIII: 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.
Source: CRISP
Glycogen storage disease type VIII: 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.
Source: MeSH 2007
These medical condition or symptom topics may be relevant to medical information for Glycogen storage disease type VIII:
Glycogen storage disease type VIII: Another name for Glycogenosis type 8 (or close medical condition association).
»Introduction: Glycogenosis type 8
»Symptoms of Glycogenosis type 8
Glycogen storage disease type VIII: Glycogen storage disease type VIII is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of Glycogen storage disease type VIII incude:
See full list of 6 symptoms of Glycogen storage disease type VIII (Glycogenosis type 8)
Source - MeSH 2007
Source - MeSH 2007
Source - CRISP
Source: CRISP
The following list attempts to classify Glycogen storage disease type VIII into categories where each line is subset of the next.
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