Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Sphingolipidosis
Gangliosidosis
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.
-
GM2 gangliosidosis 14 trials · 19 incl. sub-types Sub-types →
-
GM1 gangliosidosis 12 trials Sub-types →