Mannosidase Deficiency Diseases
"Mannosidase Deficiency Diseases" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
| Descriptor ID |
D044904
|
| MeSH Number(s) |
C16.320.565.202.607 C16.320.565.595.577 C18.452.648.202.607 C18.452.648.595.577
|
| Concept/Terms |
Mannosidase Deficiency Diseases- Mannosidase Deficiency Diseases
- Deficiency Disease, Mannosidase
- Deficiency Diseases, Mannosidase
- Diseases, Mannosidase Deficiency
- Mannosidase Deficiency Disease
- Mannosidase Deficiency Syndromes
- Deficiency Syndrome, Mannosidase
- Deficiency Syndromes, Mannosidase
- Mannosidase Deficiency Syndrome
- Mannosidosis
- Mannosidoses
|
Below are MeSH descriptors whose meaning is more general than "Mannosidase Deficiency Diseases".
Below are MeSH descriptors whose meaning is more specific than "Mannosidase Deficiency Diseases".
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