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Gangliosidoses MeSH Descriptor Data 2021


MeSH Heading
Gangliosidoses
Tree 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
Unique ID
D005733
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D005733
Annotation
coordinate IM with specific ganglioside (IM) but GANGLIOSIDOSIS, GM1 and GANGLIOSIDOSES, GM2 are available
Scope Note
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.
Entry Term(s)
Ganglioside Storage Diseases
Ganglioside Storage Disorders
Gangliosidosis
Previous Indexing
Gangliosides (1966-1975)
Lipoidosis (1966-1975)
See Also
Mucolipidoses
Public MeSH Note
1992; see GANGLIOSIDOSIS 1976-91
History Note
1992(1976)
Date Established
1976/01/01
Date of Entry
1975/07/23
Revision Date
2010/06/25
Gangliosidoses Preferred
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