OnlineIMD
20.1 Disorders of sphingolipid degradation
Type
Group
Disease group(s)
20 Disorders of complex molecule degradation
Child entries
Gaucher disease
Acid sphingomyelinase deficiency
Neutral sphingomyelinase 3 deficiency
GM1 gangliosidosis
GM2 gangliosidosis
GM2 gangliosidosis infantile form
Krabbe disease
Metachromatic leukodystrophy
Multiple sulfatase deficiency
Fabry disease
Farber disease
Saposin deficiency