Concept information
Preferred term
beta-N-Acetylhexosaminidases
Type
-
Topical Descriptor
Broader concept
Narrower concepts
Entry terms
- beta Hexosaminidase
- beta-Hexosaminidase
- beta N Acetyl D hexosaminidase
- beta-N-Acetyl-D-hexosaminidase
- beta N Acetyl hexosaminidase
- beta N Acetylhexosaminidase
- beta-N-Acetyl-hexosaminidase
- beta-N-Acetylhexosaminidase
- N Acetyl beta D hexosaminidase
- N-Acetyl-beta-D-hexosaminidase
Note
- do not confuse with ACETYLGLUCOSAMINIDASE; /defic: consider also TAY SACHS DISEASE and SANDHOFF DISEASE
Scope note
- A hexosaminidase specific for non-reducing N-acetyl-D-hexosamine residues in N-acetyl-beta-D-hexosaminides. It acts on GLUCOSIDES; GALACTOSIDES; and several OLIGOSACCHARIDES. Two specific mammalian isoenzymes of beta-N-acetylhexoaminidase are referred to as HEXOSAMINIDASE A and HEXOSAMINIDASE B. Deficiency of the type A isoenzyme causes TAY-SACHS DISEASE, while deficiency of both A and B isozymes causes SANDHOFF DISEASE. The enzyme has also been used as a tumor marker to distinguish between malignant and benign disease.
History note
- 2008(1988)
In other languages
-
Finnish
-
beeta-N-asetyyliheksoaminidaasi
-
Swedish
URI
http://www.yso.fi/onto/mesh/D001619
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