Gangliosidoses
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.
Year introduced: 1992(1976)
PubMed search builder options
Subheadings:
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, C18.452.584.563.641.803.350, C18.452.648.189.435.825.300, C18.452.648.398.641.803.350, C18.452.648.595.554.825.300
MeSH Unique ID: D005733
Entry Terms:
- Gangliosidosis
- Ganglioside Storage Diseases
- Ganglioside Storage Disease
- Storage Disease, Ganglioside
- Storage Diseases, Ganglioside
- Ganglioside Storage Disorders
- Ganglioside Storage Disorder
- Storage Disorder, Ganglioside
- Storage Disorders, Ganglioside
Previous Indexing:
See Also: