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Gaucher disease

LC control no.sh 85053526
LC classificationRC632.G36
Topical headingGaucher disease
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Variant(s)Cerebroside lipidosis
Familial splenic anemia
Gaucher's disease
Gaucher-Schlagenhaufer syndrome
Splenic anemia, Familial
See alsoCerebrosides--Metabolism--Disorders
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Sphingolipidoses
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Found inMeSH, viewed June 8, 2018 (An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM)