Structured Summary
Abstract
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.
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Classification
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Synonyms
9 entry terms
- Ganglioside Storage Diseases
- Ganglioside Storage Disorders
- Gangliosidosis
- Ganglioside Storage Disease
- Ganglioside Storage Disorder
- Storage Disease, Ganglioside
- Storage Diseases, Ganglioside
- Storage Disorder, Ganglioside
- Storage Disorders, Ganglioside
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
Indexing Annotation
coordinate IM with specific ganglioside (IM) but GANGLIOSIDOSIS, GM1 and GANGLIOSIDOSES, GM2 are available
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History Note
1992(1976)
MeSH Record
Previous Indexing
- Gangliosides (1966-1975)
- Lipoidosis (1966-1975)
MeSH Hierarchy
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AMA Style
References
- National Library of Medicine. Gangliosidoses. Medical Subject Headings (MeSH). 2026. Unique ID D005733. http://id.nlm.nih.gov/mesh/2026/D005733
- Gangliosidoses. In: Wikipedia. https://en.wikipedia.org/wiki/Gangliosidosis
- Gangliosidoses. In: Wikidata. https://www.wikidata.org/wiki/Q1493513