Structured Summary
Abstract
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.
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Classification
Broader headings
Related Concepts
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See Also
MeSH Record
Synonyms
15 entry terms
- Maltase
- Maltase-Glucoamylase
- Maltases
- alpha-Glucosidase
- Maltase Glucoamylase
- alpha Glucosidase
- alpha Glucosidases
- Acid Maltase
- Lysosomal alpha-Glucosidase
- Neutral Maltase
- Neutral alpha-Glucosidase
- Lysosomal alpha Glucosidase
- Neutral alpha Glucosidase
- alpha-Glucosidase, Lysosomal
- alpha-Glucosidase, Neutral
MeSH Record
Aspects Covered
28 allowable subheadings
Indexed with the subheadings administration & dosage, adverse effects, analysis, biosynthesis, blood, cerebrospinal fluid, chemical synthesis, chemistry, classification, deficiency, drug effects, economics, genetics, history, immunology, isolation & purification, metabolism, pharmacokinetics, pharmacology, physiology, poisoning, radiation effects, standards, supply & distribution, therapeutic use, toxicity, ultrastructure, urine.
MeSH Record
Indexing Annotation
defic/: consider also GLYCOGEN STORAGE DISEASE TYPE II
MeSH Record
History Note
1987(1978)
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Previous Indexing
- Glucosidases (1966-1977)
MeSH Hierarchy
Tree Number
MeSH Record
NLM Classification
QU 136
AMA Style
References
- National Library of Medicine. alpha-Glucosidases. Medical Subject Headings (MeSH). 2026. Unique ID D000520. http://id.nlm.nih.gov/mesh/2026/D000520
- alpha-Glucosidases. In: Wikipedia. https://en.wikipedia.org/wiki/%CE%91-Glucosidase
- alpha-Glucosidases. In: Wikidata. https://www.wikidata.org/wiki/Q2839456