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MeSH 搜索器

Gangliosidoses, GM2

A group of recessively inherited diseases characterized by the intralysosomal accumulation of G(M2) GANGLIOSIDE in the neuronal cells. Subtypes include mutations of enzymes in the BETA-N-ACETYLHEXOSAMINIDASES system or G(M2) ACTIVATOR PROTEIN leading to disruption of normal degradation of GANGLIOSIDES, a subclass of ACIDIC GLYCOSPHINGOLIPIDS.
推出的年份: 2007(2000)
副标题
树号: C10.228.140.163.100.435.825.300.300, C16.320.565.189.435.825.300.300, C16.320.565.398.641.803.350.300, C16.320.565.595.554.825.300.300, C18.452.132.100.435.825.300.300, C18.452.584.563.641.803.350.300, C18.452.648.189.435.825.300.300, C18.452.648.398.641.803.350.300, C18.452.648.595.554.825.300.300
MeSH 单一 ID: D020143
进入的组:
  • GM2 Gangliosidose
  • Gangliosidose, GM2
  • GM2 Gangliosidosis
  • GM2 Gangliosidoses
  • Gangliosidosis, GM2
  • Gangliosidoses GM2
  • GM2, Gangliosidoses
  • G(M2) Gangliosidoses
早前的内容:
  • Sandhoff Disease (1966-1999)
  • Tay-Sachs Disease (1966-1999)

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