URI(s)
- http://id.loc.gov/authorities/subjects/sh85053526
- http://id.loc.gov/authorities/sh85053526#concept
Variants
- Cerebroside lipidosis
- Familial splenic anemia
- Gaucher's disease
- Gaucher-Schlagenhaufer syndrome
- Splenic anemia, Familial
Broader Terms
Closely Matching Concepts from Other Schemes
Earlier Established Forms
- Gaucher's disease
Sources
- found: 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)
LC Classification
- RC632.G36
Instance Of
Scheme Membership(s)
Collection Membership(s)
Change Notes
- 1986-02-11: new
- 2018-07-13: revised
Alternate Formats
