Sandhoff disease (Q917227)

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lysosomal storage disorder from the GM2 gangliosidosis family, characterised by central nervous system degeneration
  • Sandhoff disease (disorder)
  • Sandhoff Jatzkewitz disease
  • Sandhoff Disease, Juvenile Type
  • Hexosaminidases a and B Deficiency
  • Gm2-Gangliosidosis, Type 2
  • GM2 gangliosidosis 0 variant
  • SANDHOFF DISEASE
  • Sandhoff Disease, Adult Type
  • Sandhoff Disease, Infantile Type
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English
Sandhoff disease
lysosomal storage disorder from the GM2 gangliosidosis family, characterised by central nervous system degeneration
  • Sandhoff disease (disorder)
  • Sandhoff Jatzkewitz disease
  • Sandhoff Disease, Juvenile Type
  • Hexosaminidases a and B Deficiency
  • Gm2-Gangliosidosis, Type 2
  • GM2 gangliosidosis 0 variant
  • SANDHOFF DISEASE
  • Sandhoff Disease, Adult Type
  • Sandhoff Disease, Infantile Type

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