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Descriptor English: alpha-Glucosidases
Descriptor Spanish: alfa-Glucosidasas
Descriptor alfa-glucosidasas
Entry term(s) alfa-glucosidasa lisosómica
glucosidasas alfa
maltasa
maltasa ácida
maltasas
Scope note: Enzimas que catalizan la exohidrólisis de los enlaces 1,4-alfa-glucosídicos con liberación de alfa-glucosa. La deficiencia de alfa-1,4-glucosidasa puede causar la ENFERMEDAD POR ALMACENAMIENTO DE GLUCÓGENO TIPO II.
Descriptor Portuguese: alfa-Glucosidases
Descriptor French: alpha-Glucosidase
Entry term(s): Acid Maltase
Lysosomal alpha Glucosidase
Lysosomal alpha-Glucosidase
Maltase
Maltase Glucoamylase
Maltase-Glucoamylase
Maltases
Neutral Maltase
Neutral alpha Glucosidase
Neutral alpha-Glucosidase
alpha Glucosidase
alpha Glucosidases
alpha-Glucosidase
alpha-Glucosidase, Lysosomal
alpha-Glucosidase, Neutral
Tree number(s): D08.811.277.450.420.050
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D000520
Scope note: Enzymes that catalyze the exohydrolysis of 1,4-alpha-glucosidic linkages with release of alpha-glucose. Deficiency of alpha-1,4-glucosidase may cause GLYCOGEN STORAGE DISEASE TYPE II.
Annotation: defic/: consider also GLYCOGEN STORAGE DISEASE TYPE II
Allowable Qualifiers: AD administration & dosage
AE adverse effects
AN analysis
BI biosynthesis
BL blood
CF cerebrospinal fluid
CH chemistry
CL classification
CS chemical synthesis
DE drug effects
DF deficiency
EC economics
GE genetics
HI history
IM immunology
IP isolation & purification
ME metabolism
PD pharmacology
PH physiology
PK pharmacokinetics
PO poisoning
RE radiation effects
SD supply & distribution
ST standards
TO toxicity
TU therapeutic use
UL ultrastructure
UR urine
Entry Combination: antagonists & inhibitors:Glycoside Hydrolase Inhibitors
Registry Number: EC 3.2.1.20
CAS Type 1 Name: alpha-D-Glucoside glucohydrolases
Previous Indexing: Glucosidases (1966-1977)
Public MeSH Note: 1987; see GLUCOSIDASES 1978-1986, for LYSOSOMAL ALPHA-GLUCOSIDASE & ACID MALTASE see GLUCAN 1,4-ALPHA-GLUCOSIDASE 1978-2006
History Note: 1987(1978)
Related: Glycogen Storage Disease Type II MeSH
DeCS ID: 520
Unique ID: D000520
NLM Classification: QU 136
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1987/01/01
Date of Entry: 1977/04/15
Revision Date: 2020/05/27
alpha-Glucosidases - Preferred
Concept UI M0000794
Scope note Enzymes that catalyze the exohydrolysis of 1,4-alpha-glucosidic linkages with release of alpha-glucose. Deficiency of alpha-1,4-glucosidase may cause GLYCOGEN STORAGE DISEASE TYPE II.
Preferred term alpha-Glucosidases
Entry term(s) Maltase
Maltase Glucoamylase
Maltase-Glucoamylase
Maltases
alpha Glucosidase
alpha Glucosidases
alpha-Glucosidase
Lysosomal alpha-Glucosidase - Narrower
Concept UI M0497620
Preferred term Lysosomal alpha-Glucosidase
Entry term(s) Acid Maltase
Lysosomal alpha Glucosidase
alpha-Glucosidase, Lysosomal
Neutral alpha-Glucosidase - Narrower
Concept UI M0000795
Preferred term Neutral alpha-Glucosidase
Entry term(s) Neutral Maltase
Neutral alpha Glucosidase
alpha-Glucosidase, Neutral



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