G(M2) Ganglioside
"G(M2) Ganglioside" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
| Descriptor ID |
D005678
|
| MeSH Number(s) |
D09.400.410.420.025.475.400 D10.390.470.025.475.400 D10.570.877.360.025.475.400
|
| Concept/Terms |
G(M2) Ganglioside- G(M2) Ganglioside
- Ganglioside GM2
- GM2, Ganglioside
- Tay-Sachs Disease Ganglioside
- Ganglioside, Tay-Sachs Disease
- Tay Sachs Disease Ganglioside
|
Below are MeSH descriptors whose meaning is more general than "G(M2) Ganglioside".
Below are MeSH descriptors whose meaning is more specific than "G(M2) Ganglioside".
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Below are the most recent publications written about "G(M2) Ganglioside" by people in Profiles.