Gangliosidoses, GM2

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"Gangliosidoses, GM2" 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 group of recessively inherited diseases characterized by the intralysosomal accumulation of G(M2) GANGLIOSIDE in the neuronal cells. Subtypes include mutations of enzymes in the BETA-N-ACETYLHEXOSAMINIDASES system or G(M2) ACTIVATOR PROTEIN leading to disruption of normal degradation of GANGLIOSIDES, a subclass of ACIDIC GLYCOSPHINGOLIPIDS.

Descriptor ID	D020143
MeSH Number(s)	C10.228.140.163.100.435.825.300.300 C16.320.565.189.435.825.300.300 C16.320.565.398.641.803.350.300 C16.320.565.595.554.825.300.300 C18.452.132.100.435.825.300.300 C18.452.584.687.803.350.300 C18.452.648.189.435.825.300.300 C18.452.648.398.641.803.350.300 C18.452.648.595.554.825.300.300
Concept/Terms	Gangliosidoses, GM2 Gangliosidoses, GM2 GM2 Gangliosidose Gangliosidose, GM2 Gangliosidoses GM2 GM2, Gangliosidoses G(M2) Gangliosidoses GM2 Gangliosidosis GM2 Gangliosidoses Gangliosidosis, GM2

Below are MeSH descriptors whose meaning is more general than "Gangliosidoses, GM2".

Diseases [C]
Nervous System Diseases [C10]
Central Nervous System Diseases [C10.228]
Brain Diseases [C10.228.140]
Brain Diseases, Metabolic [C10.228.140.163]
Brain Diseases, Metabolic, Inborn [C10.228.140.163.100]
Lysosomal Storage Diseases, Nervous System [C10.228.140.163.100.435]
Sphingolipidoses [C10.228.140.163.100.435.825]
Gangliosidoses [C10.228.140.163.100.435.825.300]
Gangliosidoses, GM2 [C10.228.140.163.100.435.825.300.300]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Metabolism, Inborn Errors [C16.320.565]
Brain Diseases, Metabolic, Inborn [C16.320.565.189]
Lysosomal Storage Diseases, Nervous System [C16.320.565.189.435]
Sphingolipidoses [C16.320.565.189.435.825]
Gangliosidoses [C16.320.565.189.435.825.300]
Gangliosidoses, GM2 [C16.320.565.189.435.825.300.300]
Lipid Metabolism, Inborn Errors [C16.320.565.398]
Lipidoses [C16.320.565.398.641]
Sphingolipidoses [C16.320.565.398.641.803]
Gangliosidoses [C16.320.565.398.641.803.350]
Gangliosidoses, GM2 [C16.320.565.398.641.803.350.300]
Lysosomal Storage Diseases [C16.320.565.595]
Lysosomal Storage Diseases, Nervous System [C16.320.565.595.554]
Sphingolipidoses [C16.320.565.595.554.825]
Gangliosidoses [C16.320.565.595.554.825.300]
Gangliosidoses, GM2 [C16.320.565.595.554.825.300.300]
Nutritional and Metabolic Diseases [C18]
Metabolic Diseases [C18.452]
Brain Diseases, Metabolic [C18.452.132]
Brain Diseases, Metabolic, Inborn [C18.452.132.100]
Lysosomal Storage Diseases, Nervous System [C18.452.132.100.435]
Sphingolipidoses [C18.452.132.100.435.825]
Gangliosidoses [C18.452.132.100.435.825.300]
Gangliosidoses, GM2 [C18.452.132.100.435.825.300.300]
Lipid Metabolism Disorders [C18.452.584]
Lipidoses [C18.452.584.687]
Sphingolipidoses [C18.452.584.687.803]
Gangliosidoses [C18.452.584.687.803.350]
Gangliosidoses, GM2 [C18.452.584.687.803.350.300]
Metabolism, Inborn Errors [C18.452.648]
Brain Diseases, Metabolic, Inborn [C18.452.648.189]
Lysosomal Storage Diseases, Nervous System [C18.452.648.189.435]
Sphingolipidoses [C18.452.648.189.435.825]
Gangliosidoses [C18.452.648.189.435.825.300]
Gangliosidoses, GM2 [C18.452.648.189.435.825.300.300]
Lipid Metabolism, Inborn Errors [C18.452.648.398]
Lipidoses [C18.452.648.398.641]
Sphingolipidoses [C18.452.648.398.641.803]
Gangliosidoses [C18.452.648.398.641.803.350]
Gangliosidoses, GM2 [C18.452.648.398.641.803.350.300]
Lysosomal Storage Diseases [C18.452.648.595]
Lysosomal Storage Diseases, Nervous System [C18.452.648.595.554]
Sphingolipidoses [C18.452.648.595.554.825]
Gangliosidoses [C18.452.648.595.554.825.300]
Gangliosidoses, GM2 [C18.452.648.595.554.825.300.300]

Below are MeSH descriptors whose meaning is related to "Gangliosidoses, GM2".

Below are MeSH descriptors whose meaning is more specific than "Gangliosidoses, GM2".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Gangliosidoses, GM2" by people in UAMS Profiles by year, and whether "Gangliosidoses, GM2" was a major or minor topic of these publications.

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