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Gaucher's disease (Q861645)

From Wikidata
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)
  • lipoid histiocytosis
  • Glucocerebrosidase deficiency
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    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)
    • lipoid histiocytosis
    • Glucocerebrosidase deficiency

    Statements

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    0.00001225±0.00000525
    Gaucher's disease
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    Identifiers

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