G(M2) Ganglioside
A glycosphingolipid that accumulates due to a deficiency of hexosaminidase A or B (BETA-N-ACETYLHEXOSAMINIDASES), or GM2 activator protein, resulting in GANGLIOSIDOSES, heredity metabolic disorders that include TAY-SACHS DISEASE and SANDHOFF DISEASE.
Year introduced: 1991(1975)
PubMed search builder options
Subheadings:
Tree Number(s): D09.400.410.420.025.475.400, D10.390.470.025.475.400, D10.570.877.360.025.475.400
MeSH Unique ID: D005678
Registry Number: 19600-01-2
Entry Terms:
- GM2 Ganglioside
- Ganglioside, GM2
- Tay-Sachs Disease Ganglioside
- Ganglioside, Tay-Sachs Disease
- Tay Sachs Disease Ganglioside
- Ganglioside GM2
- GM2, Ganglioside
Previous Indexing:
See Also: