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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)

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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

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