A group of autosomal recessive lysosomal storage disorders marked by the accumulation of GANGLIOSIDES. They are caused by impaired enzymes or defective cofactors required for normal ganglioside degradation in the LYSOSOMES. Gangliosidoses are classified by the specific ganglioside accumulated in the defective degradation pathway.
Synonyms: Ganglioside Storage Disorder, Gangliosidosis, Storage Disorder, Ganglioside, Storage Disease, Ganglioside, Ganglioside Storage Disorders, Storage Diseases, Ganglioside, Ganglioside Storage Diseases, Storage Disorders, Ganglioside, Ganglioside Storage Disease, Gangliosidoses
Instance information
1992; see GANGLIOSIDOSIS 1976-91 ,1992(1976) ,coordinate IM with specific ganglioside (IM) but GANGLIOSIDOSIS, GM1 and GANGLIOSIDOSES, GM2 are available
D005733