sphingolipidosis
class of lipid storage disorders relating to sphingolipid metabolism
Krabbe disease
congenital disorder of the nervous system
Gaucher's disease
human disease characterized by deficiency of the enzyme glucocerebrosidase which results in the accumulation of harmful quantities of the glycolipid glucocerebroside throughout the body
Fabry disease
rare human genetic lysosomal storage disorder
Niemann-Pick disease
severe metabolic disorders in which sphingomyelin accumulates in lysosomes in cells