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MeSH 搜索器

Gangliosidoses

A group of autosomal recessive lysosomal storage disorders marked by the accumulation of GANGLIOSIDES. They are caused by impaired enzymes or defective cofactors required for normal ganglioside degradation in the LYSOSOMES. Gangliosidoses are classified by the specific ganglioside accumulated in the defective degradation pathway.
推出的年份: 1992(1976)
副标题
树号: C10.228.140.163.100.435.825.300, C16.320.565.189.435.825.300, C16.320.565.398.641.803.350, C16.320.565.595.554.825.300, C18.452.132.100.435.825.300, C18.452.584.563.641.803.350, C18.452.648.189.435.825.300, C18.452.648.398.641.803.350, C18.452.648.595.554.825.300
MeSH 单一 ID: D005733
进入的组:
  • Ganglioside Storage Disorders
  • Ganglioside Storage Disorder
  • Storage Disorder, Ganglioside
  • Storage Disorders, Ganglioside
  • Ganglioside Storage Diseases
  • Ganglioside Storage Disease
  • Storage Disease, Ganglioside
  • Storage Diseases, Ganglioside
  • Gangliosidosis
早前的内容:
  • Gangliosides (1966-1975)
  • Lipoidosis (1966-1975)

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