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Gaucher Disease |
Anemia, splenic, familial; Cerebroside Lipidosis Syndrome; Glucocerebrosidase deficiency; Glucocerebrosidosis; Glucosyl cerebroside lipidosis; Glucosylceramidase deficiency; Glucosylceramide beta-glucosidase deficiency; Glucosylceramide lipidosis; Kerasin histiocytosis; Kerasin lipoidosis; Kerasin thesaurismosis; Lipidosis, cerebroside; Lipoid histiocytosis (kerasin type) |
Gaucher's disease Retrieved from "http://en.wikipedia.org/wiki/Gaucher_disease" ...
Wikipedia - [full article]
Gaucher Disease Articles
- Gaucher disease
... Gaucher disease is an inherited disorder in which the body cannot break down a lipid called glucocerebroside. Genetic changes are related to the following types of Gaucher disease. Gaucher disease, ty... - Gaucher's Disease Information Page
... Gaucher disease is an inherited metabolic disorder in which harmful quantities of a fatty substance called glucocerebroside accumulate in the spleen, liver, lungs, bone marrow, and, in rare cases, the...
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