(Q917227)

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

Statements

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