Gaucher Disease Community

Community Statistics

Discussion Topics: 1
Community Members: 11

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, Subset of Lysosomal Storage Disease

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Community Members

1. 

   OverloadedMama

   

   EBMResearch

   

   gocsi

   

   Pattyt

   

   amf1

2. 

   Gaucher

   

   Nancefeve

   

   lleber

   

   nananeliz

   

   writeawaynyc

3. 

   tony123