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- Bfb1684e4b27551da5c9364489ba20990 hasDbXref "MESH:D005733" @default.
- Bfb1684e4b27551da5c9364489ba20990 type Axiom @default.
- Bfb1684e4b27551da5c9364489ba20990 annotatedProperty IAO_0000115 @default.
- Bfb1684e4b27551da5c9364489ba20990 annotatedSource MONDO_0017719 @default.
- Bfb1684e4b27551da5c9364489ba20990 annotatedTarget "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." @default.