Gaucher's disease (Q861645)

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human disease characterized by deficiency of the enzyme glucocerebrosidase which results in the accumulation of harmful quantities of the glycolipid glucocerebroside throughout the body
  • Gaucher disease
  • acid beta-glucosidase deficiency
  • glocucerebrosidase deficiency
  • glucosylceramide beta-glucosidase deficiency
  • kerasin thesaurismosis
  • lipoid histiocytosis (kerasin type)
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Language Label Description Also known as
English
Gaucher's disease
human disease characterized by deficiency of the enzyme glucocerebrosidase which results in the accumulation of harmful quantities of the glycolipid glucocerebroside throughout the body
  • Gaucher disease
  • acid beta-glucosidase deficiency
  • glocucerebrosidase deficiency
  • glucosylceramide beta-glucosidase deficiency
  • kerasin thesaurismosis
  • lipoid histiocytosis (kerasin type)

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