Gangliosidosis contains different types of lipid storage disorders caused by the accumulation of lipids known as gangliosides. There are two distinct genetic causes of the disease. Both are autosomal recessive and affect males and females equally.
GM1 gangliosidoses - GM1
GM2 gangliosidoses - GM2
Sphingolipidoses#Overview for an overview table, including gangliosidosis
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