Concept information
Preferred term
Hexosaminidase B
Type
-
Topical Descriptor
Broader concept
Narrower concepts
Entry terms
- Hex B
Scope note
- A mammalian beta-hexosaminidase isoform that is comprized of hexosaminidase beta subunits. Deficiency of hexosaminidase B due to mutations in the gene encoding the hexosaminidase beta subunit is a case of SANDHOFF DISEASE.
History note
- 2008; use BETA-N-ACETYLHEXOSAMINIDASES 1987-2007
In other languages
-
Finnish
-
HEX B
-
Swedish
URI
http://www.yso.fi/onto/mesh/D054819
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