LC control no. | sh 85053526 |
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LC classification | RC632.G36 |
Topical heading | Gaucher disease |
Variant(s) | Cerebroside lipidosis Familial splenic anemia Gaucher's disease Gaucher-Schlagenhaufer syndrome Splenic anemia, Familial |
See also | Cerebrosides--Metabolism--Disorders Sphingolipidoses |
Found in | MeSH, 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) |