Glycogen Storage Disease Type IIb

"Glycogen Storage Disease Type IIb" 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

An X-linked dominant multisystem disorder resulting in cardiomyopathy, myopathy and INTELLECTUAL DISABILITY. It is caused by mutation in the gene encoding LYSOSOMAL-ASSOCIATED MEMBRANE PROTEIN 2.

Descriptor ID	D052120
MeSH Number(s)	C10.597.606.643.455.562 C14.280.238.458 C16.320.322.201 C16.320.565.202.449.510 C18.452.648.202.449.510
Concept/Terms	Glycogen Storage Disease Type IIb Glycogen Storage Disease Type IIb Danon Disease Glycogen Storage Cardiomyopathy Cardiomyopathies, Glycogen Storage Cardiomyopathy, Glycogen Storage Glycogen Storage Cardiomyopathies Glycogen Storage Disease IIb Glycogen Storage Disease Limited to the Heart Lysosomal Glycogen Storage Disease with Normal Acid Maltase Lysosomal Glycogen Storage Disease without Acid Maltase Deficiency Pseudoglycogenosis 2 Pseudoglycogenosis 2s Pseudoglycogenosis II Pseudoglycogenosis IIs Vacuolar Cardiomyopathy and Myopathy, X-linked Vacuolar Cardiomyopathy and Myopathy, X linked X-Linked Vacuolar Cardiomyopathy and Myopathy X Linked Vacuolar Cardiomyopathy and Myopathy Antopol Disease Disease, Antopol Glycogen Storage Disease Type 2B

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

Diseases [C]
Nervous System Diseases [C10]
Neurologic Manifestations [C10.597]
Neurobehavioral Manifestations [C10.597.606]
Intellectual Disability [C10.597.606.643]
Mental Retardation, X-Linked [C10.597.606.643.455]
Glycogen Storage Disease Type IIb [C10.597.606.643.455.562]
Cardiovascular Diseases [C14]
Heart Diseases [C14.280]
Cardiomyopathies [C14.280.238]
Glycogen Storage Disease Type IIb [C14.280.238.458]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Genetic Diseases, X-Linked [C16.320.322]
Glycogen Storage Disease Type IIb [C16.320.322.201]
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 IIb [C16.320.565.202.449.510]
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 IIb [C18.452.648.202.449.510]

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

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

publications

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