Acid Ceramidase [kyselá ceramidasa]
- Terms
-
kyselá ceramidáza
A ceramidase subtype that is active at acid pH. It plays an important role in sphingolipid degradation by catalyzing the lysosomal hydrolysis of ceramide to sphingosine and free fatty acid. Inherited deficiency of acid ceramidase activity results in FARBER LIPOGRANULOMATOSIS.
- DUI
- D055573 MeSH Browser
- CUI
- M0518530
- Previous indexing
- Galactosylgalactosylglucosylceramidase (1974-2008)
- History note
- 2009(1982); use GALACTOSYLGALACTOSYLGLUCOSYLCERAMIDASE 1983-2008
- Public note
- 2009; see CERAMIDE TRIHEXOSIDASE 1983-2008
Combination
- deficiency
- Farber Lipogranulomatosis
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 4
- HI
- history
- IM
- immunology
- IP
- isolation & purification
- ME
- metabolism 4
- PK
- pharmacokinetics
- PD
- pharmacology
- PH
- physiology 1
- PO
- poisoning
- RE
- radiation effects
- ST
- standards
- SD
- supply & distribution
- TU
- therapeutic use
- TO
- toxicity
- UL
- ultrastructure
- UR
- urine
ASAH1 protein, human Chemical MeSH Browser
Asah1 protein, mouse Chemical MeSH Browser
Asah1 protein, rat Chemical MeSH Browser