Glycogen Storage Disease Type VI

A hepatic GLYCOGEN STORAGE DISEASE in which there is an apparent deficiency of hepatic phosphorylase (GLYCOGEN PHOSPHORYLASE, LIVER FORM) activity.

Year introduced: 1991(1989)

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Tree Number(s): C16.320.565.202.449.580, C18.452.648.202.449.580

MeSH Unique ID: D006013

Entry Terms:

• Glycogenosis Type VI
• Type VI, Glycogenosis
• Glycogenosis VI
• Hers Disease
• Disease, Hers
• Glycogenosis 6
• Hepatic Glycogen Phosphorylase Deficiency
• Liver Phosphorylase Deficiency Syndrome
• Hers' Disease
• Disease, Hers'
• Her Disease

Previous Indexing:

• Glucosyltransferases/metabolism (1966-1974)
• Glycogenosis (1966-1974)
• Liver Diseases (1966-1974)

See Also:

• Glycogen Phosphorylase, Liver Form

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Glycogen Storage Disease
Glycogen Storage Disease Type VI

All MeSH Categories
Diseases Category
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Glycogen Storage Disease
Glycogen Storage Disease Type VI