Gaucher's disease

Name(s): 
Gaucher disease
Nature 
A lipid storage disease linked to a single recessive gene particularly common in Jews of Eastern European ancestry. Gaucher disease results from a specific enzyme deficiency in the body, caused by a genetic mutation received from both parents. The disease course is quite variable, ranging from no outward symptoms to severe disability and death.
Reduced by 
Strategy(ies) 
Value(s) 
Type 
(E) Emanations of other problems