Hexosaminidase B [hexosaminidasa B]
topical
1
- Terms
-
Hex B
hexosaminidáza B
hexozaminidáza B
-
Hex B
Persistent link
https://www.medvik.cz/link/D054819
Definition
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.
- DUI
- D054819 MeSH Browser
- CUI
- M0002424
- Previous indexing
- beta-N-Acetylhexosaminidases (1987-2007)
- History note
- 2008; use BETA-N-ACETYLHEXOSAMINIDASES 1987-2007
- Public note
- 2008; see BETA-N-ACETYLHEXOSAMINIDASE 1987-2007
Combination
- deficiency
- Sandhoff Disease
Allowable subheadings
- AD
- administration & dosage
- AE
- adverse effects
- AN
- analysis
- AI
- antagonists & inhibitors
- BI
- biosynthesis
- BL
- blood
- CF
- cerebrospinal fluid
- CS
- chemical synthesis
- CH
- chemistry
- CL
- classification
- DE
- drug effects
- EC
- economics
- GE
- genetics 1
- HI
- history
- IM
- immunology
- IP
- isolation & purification
- ME
- metabolism
- PK
- pharmacokinetics
- PD
- pharmacology
- PH
- physiology
- PO
- poisoning
- RE
- radiation effects
- ST
- standards
- SD
- supply & distribution
- TU
- therapeutic use
- TO
- toxicity
- UL
- ultrastructure
- UR
- urine
...
Occurrences in Medvik records
D
Chemicals and Drugs