Gaucher's disease or Gaucher disease (/ɡoʊˈʃeɪ/) (GD) is a genetic disorder in which glucocerebroside (a sphingolipid, also known as glucosylceramide)...

glucocerebrosidase gene each cause Gaucher's disease in Ashkenazim, which is that group's most common genetic disease, but only one of these mutations is...

leukemia, polycythemia vera, pernicious anemia, Gaucher's disease, leishmaniasis, Hodgkin's disease, Banti's disease, hereditary spherocytosis, cysts, glandular...

who had Gaucher's disease. He was scheduled for a spleen removal but his mother pleaded with Roscoe Brady, MD, and expert in Gaucher's disease, to include...

and neuronal cell death. Gaucher's disease Lysosomal storage disease Medical genetics of Ashkenazi Jews Niemann–Pick disease, type C "Niemann–Pick". Oxford...

spectrophotometry. A defect in the degradation of glucocerebrosides is Gaucher's disease. The corresponding defects for galactocerebrosides are: a) Ceramide...

myelofibrosis and metabolic abnormalities such as Gaucher's disease and glycogen storage diseases.[citation needed] Portal hypertension Ascites Hypersplenism...

the brand name Cerdelga, is a medication used for the treatment of Gaucher's disease. It was discovered at the University of Michigan, developed by Genzyme...

Parkinson's disease, dystonia, cerebral palsy, Alzheimer's disease, Gaucher's disease, subacute sclerosing panencephalitis, Creutzfeldt–Jakob disease (CJD)...

cerebrosides in which the monosaccharide head group is glucose. In Gaucher's disease, the enzyme glucocerebrosidase is nonfunctional and cannot break down...