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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

URI

http://data.loterre.fr/ark:/67375/JVR-HL3R5V2J-T

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RDF/XML TURTLE JSON-LD Creado 19/11/74, última modificación 22/3/19