Catalog

GM1 gangliosidosis

No MMS code

Link to WHO Definition

GM1 gangliosidosis – http://id.who.int/icd/entity/401105928

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.

Parents

Children