Structured Summary
Abstract
Diseases caused by the loss of one or more enzymes involved in the hydrolysis of mannoside linkages (MANNOSIDASES). The defects in enzyme activity are primarily associated with genetic mutation of the genes that codes for a particular mannosidase isoenzyme.
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Synonyms
10 entry terms
- Mannosidase Deficiency Syndromes
- Mannosidosis
- Deficiency Disease, Mannosidase
- Deficiency Diseases, Mannosidase
- Deficiency Syndrome, Mannosidase
- Deficiency Syndromes, Mannosidase
- Diseases, Mannosidase Deficiency
- Mannosidase Deficiency Disease
- Mannosidase Deficiency Syndrome
- Mannosidoses
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Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
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History Note
2004; use MANNOSIDOSIS, ALPHA B, LYSOSOMAL 1984-2003
MeSH Record
Previous Indexing
- Mannosidosis (1984-2003)
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AMA Style
References
- National Library of Medicine. Mannosidase Deficiency Diseases. Medical Subject Headings (MeSH). 2026. Unique ID D044904. http://id.nlm.nih.gov/mesh/2026/D044904
- Mannosidase Deficiency Diseases. In: Wikipedia. https://en.wikipedia.org/wiki/Mannosidosis
- Mannosidase Deficiency Diseases. In: Wikidata. https://www.wikidata.org/wiki/Q6750947