What is the name of the enzyme that is deficient in individuals with Gaucher's disease, a lysosomal storage disorder characterized by the accumulation of glucocerebroside in cells?

A Glucocerebrosidase
B Hexosaminidase A
C Sphingomyelinase
D Alpha-galactosidase
Gaucher's disease is caused by a deficiency of the enzyme glucocerebrosidase, which is responsible for breaking down glucocerebroside into glucose and ceramide. The accumulation of glucocerebroside leads to the characteristic symptoms of the disease.
'Gaucher' sounds like 'go cher', go find the deficient enzyme
Scriver's The Metabolic and Molecular Bases of Inherited Disease
Enzymes in Disease Biochemistry Lysosomal Storage Disorders Hard MEDICAL Confidence: high