Sandhoff disease
lysosomal storage disorder from the GM2 gangliosidosis family, characterised by central nervous system degeneration
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Sandhoff disease
Summary
Sandhoff disease is a rare disease[1]. It has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Sandhoff disease's instance of is recorded as rare disease[3].
- Sandhoff disease's instance of is recorded as class of disease[4].
- Sandhoff disease is a type of GM2 gangliosidosis[5].
- Sandhoff disease is a type of eye degenerative disease[6].
- Sandhoff disease is a type of disease[7].
- Sandhoff disease's NCI Thesaurus ID is recorded as C85052[8].
- Sandhoff disease's health specialty is recorded as endocrinology[9].
- Sandhoff disease's genetic association is recorded as HEXB[10].
- Sandhoff disease's exact match is recorded as http://purl.obolibrary.org/obo/DOID_3323[11].
- Sandhoff disease's exact match is recorded as http://identifiers.org/doid/DOID:3323[12].
- Sandhoff disease's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_796[13].
- Sandhoff disease's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
Why It Matters
Sandhoff disease has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[2] It is known by 14 alternative names across languages and contexts.[15]