Gaucher disease (Q62034): Difference between revisions
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Revision as of 09:32, 14 August 2026
Gaucher disease is a lysosomal storage disorder by the presence of glucosylceramide (or glucocerebroside) deposits in the reticuloendothelial cells of the liver, spleen and bone marrow, and encompassing three main forms (types 1, 2 and 3), a fetal form and a variant with cardiac involvement (Gaucher disease - ophthalmoplegia - cardiovascular calcification or Gaucher-like disease).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1923566939 |
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| English | Gaucher disease |
Gaucher disease is a lysosomal storage disorder by the presence of glucosylceramide (or glucocerebroside) deposits in the reticuloendothelial cells of the liver, spleen and bone marrow, and encompassing three main forms (types 1, 2 and 3), a fetal form and a variant with cardiac involvement (Gaucher disease - ophthalmoplegia - cardiovascular calcification or Gaucher-like disease). |
