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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