Gangliosidoses

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"Gangliosidoses" 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 autosomal recessive lysosomal storage disorders marked by the accumulation of GANGLIOSIDES. They are caused by impaired enzymes or defective cofactors required for normal ganglioside degradation in the LYSOSOMES. Gangliosidoses are classified by the specific ganglioside accumulated in the defective degradation pathway.

Descriptor ID	D005733
MeSH Number(s)	C10.228.140.163.100.435.825.300 C16.320.565.189.435.825.300 C16.320.565.398.641.803.350 C16.320.565.595.554.825.300 C18.452.132.100.435.825.300 C18.452.584.687.803.350 C18.452.648.189.435.825.300 C18.452.648.398.641.803.350 C18.452.648.595.554.825.300
Concept/Terms	Gangliosidoses Gangliosidoses Ganglioside Storage Disorders Ganglioside Storage Disorder Storage Disorder, Ganglioside Storage Disorders, Ganglioside Gangliosidosis Ganglioside Storage Diseases Ganglioside Storage Disease Storage Disease, Ganglioside Storage Diseases, Ganglioside

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

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]
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]
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]
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]
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]
Lipid Metabolism Disorders [C18.452.584]
Lipidoses [C18.452.584.687]
Sphingolipidoses [C18.452.584.687.803]
Gangliosidoses [C18.452.584.687.803.350]
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]
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]
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]

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

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

publications

Timeline | Most Recent

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