GM1 gangliosidosis (Q90733)

GM1 gangliosidosis is a rare lysosomal storage disorder characterised biochemically by deficient beta-galactosidase activity and clinically by a wide range of variable neurovisceral, ophthalmological and dysmorphic features.

Language	Label	Description	Also known as
default for all languages	ID_401105928
English	GM1 gangliosidosis	GM1 gangliosidosis is a rare lysosomal storage disorder characterised biochemically by deficient beta-galactosidase activity and clinically by a wide range of variable neurovisceral, ophthalmological and dysmorphic features.