Sandhoff disease
Sign in to saveAlso 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, Sandhoff Disease, Adult Type
lysosomal storage disorder from the GM2 gangliosidosis family, characterised by central nervous system degeneration
In the Vinony graph
Vinony's link graph records 59 inbound references to Sandhoff disease, and connects out to Wolman disease, lysosome and gangliosides.
It is catalogued under topics including Autosomal recessive disorders, Diseases named after discoverers and Lipid storage disorders.
Vinony links it to 12 Wikipedia language editions.
Research
944 papers- Sandhoff Disease.1993
- Sandhoff disease in the elderly: a case study.Amyotrophic lateral sclerosis & frontotemporal degeneration · 2022
- Microglia-neuron crosstalk through Hex-GM2-MGL2 maintains brain homeostasis.Nature · 2025
- Sandhoff disease.Acta pathologica japonica · 1981
- [Lysosome disease--Sandhoff disease].Nihon rinsho. Japanese journal of clinical medicine · 1993
via PubMed
Wikidata facts
- Subclass of
- disease
Show 4 more facts
- health specialty
- endocrinology
- exact match
- www.orpha.net/ORDO/Orphanet_796
- NCI Thesaurus ID
- C85052
- on focus list of Wikimedia project
- WikiProject Medicine
via Wikidata · CC0
Connections
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lysosome
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gangliosides
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hexosaminidases
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