Concept information
Término preferido
G(M2) Ganglioside
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Tipo
-
mesh:Descriptor
Definición
- 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.
Concepto genérico
Etiquetas alternativas
- 19600-01-2
- Ganglioside GM2
- GM2 Ganglioside
- Tay-Sachs Disease Ganglioside
En otras lenguas
-
francés
-
19600-01-2
URI
http://data.loterre.fr/ark:/67375/JVR-HL3R5V2J-T
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