Also known as Sandhoff disease (disorder), Sandhoff Jatzkewitz disease, Sandhoff Disease, Juvenile Type, Hexosaminidases a and B Deficiency, Gm2-Gangliosidosis, Type 2, GM2 gangliosidosis 0 variant,
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lysosomal storage disorder from the GM2 gangliosidosis family, characterised by central nervous system degeneration
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Discovered by embedding cosine similarity (sentence-transformers MiniLM, 384-dim).