Concept information
Preferred term
beta-N-Acetylhexosaminidases
Type
-
mesh:Descriptor
Definition
- 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.
Broader concept
Narrower concepts
Entry terms
- beta-Hexosaminidase
- beta-N-Acetyl-D-hexosaminidase
- beta-N-Acetyl-D-hexosaminide N-acetylhexosaminohydrolase
- beta-N-Acetyl-hexosaminidase
- beta-N-Acetylhexosaminidase
- N-Acetyl-beta-D-hexosaminidase
Allowable Qualifier(s)
- administration & dosage (Qualifier)
- adverse effects (Qualifier)
- analysis (Qualifier)
- antagonists & inhibitors (Qualifier)
- biosynthesis (Qualifier)
- blood (Qualifier)
- cerebrospinal fluid (Qualifier)
- chemical synthesis (Qualifier)
- chemistry (Qualifier)
- classification (Qualifier)
- deficiency (Qualifier)
- drug effects (Qualifier)
- economics (Qualifier)
- genetics (Qualifier)
- history (Qualifier)
- immunology (Qualifier)
- isolation & purification (Qualifier)
- metabolism (Qualifier)
- pharmacokinetics (Qualifier)
- pharmacology (Qualifier)
- physiology (Qualifier)
- poisoning (Qualifier)
- radiation effects (Qualifier)
- standards (Qualifier)
- supply & distribution (Qualifier)
- therapeutic use (Qualifier)
- toxicity (Qualifier)
- ultrastructure (Qualifier)
- urine (Qualifier)
In other languages
-
French
-
beta-Hexosaminidase
-
beta-N-Acetyl-D-hexosaminide N-acetylhexosaminohydrolase
-
beta-N-Acetyl-hexosaminidase
-
beta-N-Acetylhexosaminidase
-
N-Acétyl-bêta-D-hexosaminidase
URI
http://data.loterre.fr/ark:/67375/JVR-M8NRMFCW-R
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