Hexosaminidase A
"Hexosaminidase A" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A mammalian beta-hexosaminidase isoform that is a heteromeric protein comprized of both hexosaminidase alpha and hexosaminidase beta subunits. Deficiency of hexosaminidase A due to mutations in the gene encoding the hexosaminidase alpha subunit is a case of TAY-SACHS DISEASE. Deficiency of hexosaminidase A and HEXOSAMINIDASE B due to mutations in the gene encoding the hexosaminidase beta subunit is a case of SANDHOFF DISEASE.
| Descriptor ID |
D054818
|
| MeSH Number(s) |
D08.811.277.450.483.180.750
|
| Concept/Terms |
Hexosaminidase A- Hexosaminidase A
- Hex A
- beta-N-Acetylhexosaminidase A
- beta N Acetylhexosaminidase A
|
Below are MeSH descriptors whose meaning is more general than "Hexosaminidase A".
Below are MeSH descriptors whose meaning is more specific than "Hexosaminidase A".
This graph shows the total number of publications written about "Hexosaminidase A" by people in UAMS Profiles by year, and whether "Hexosaminidase A" was a major or minor topic of these publications.
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Below are the most recent publications written about "Hexosaminidase A" by people in Profiles over the past ten years.