Gaucher Disease Community

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Brief Description

Gaucher Disease is a rare lysosomal storage disease characterized by the accumulation of glucocerebroside in the spleen, liver, kidneys, lungs, brain and bone marrow.

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Synonyms

Cerebroside Lipidosis Syndrome, Gaucher Splenomegaly, Glucocerebrosidase Deficiency, Glucocerebrosidosis, Glucosyl Cerebroside Lipidosis, Glucosylceramidase Deficiency, Kerasin Lipoidosis, Kerasin Thesaurismosis, Lipid Histiocytosis (Kerasin Type), Sphingolipidosis 1, Norrbottnian Gaucher Disease, Type I Gaucher Disease, Type II Gaucher Disease, Type III Gaucher Disease

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   gocsi