Glycogen Storage Disease Type VI

"Glycogen Storage Disease Type VI" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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

Descriptor ID

D006013

MeSH Number(s)

C16.320.565.202.449.580

C18.452.648.202.449.580

Concept/Terms

Glycogen Storage Disease Type VI

Below are MeSH descriptors whose meaning is more general than "Glycogen Storage Disease Type VI".

Diseases [C]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Metabolism, Inborn Errors [C16.320.565]
Carbohydrate Metabolism, Inborn Errors [C16.320.565.202]
Glycogen Storage Disease [C16.320.565.202.449]
Glycogen Storage Disease Type VI [C16.320.565.202.449.580]
Nutritional and Metabolic Diseases [C18]
Metabolic Diseases [C18.452]
Metabolism, Inborn Errors [C18.452.648]
Carbohydrate Metabolism, Inborn Errors [C18.452.648.202]
Glycogen Storage Disease [C18.452.648.202.449]
Glycogen Storage Disease Type VI [C18.452.648.202.449.580]

Below are MeSH descriptors whose meaning is related to "Glycogen Storage Disease Type VI".

Below are MeSH descriptors whose meaning is more specific than "Glycogen Storage Disease Type VI".

publications

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This graph shows the total number of publications written about "Glycogen Storage Disease Type VI" by people in Harvard Catalyst Profiles by year, and whether "Glycogen Storage Disease Type VI" was a major or minor topic of these publication.

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