alpha-Mannosidosis
"alpha-Mannosidosis" 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.
An inborn error of metabolism marked by a defect in the lysosomal isoform of ALPHA-MANNOSIDASE activity that results in lysosomal accumulation of mannose-rich intermediate metabolites. Virtually all patients have psychomotor retardation, facial coarsening, and some degree of dysostosis multiplex. It is thought to be an autosomal recessive disorder.
Descriptor ID |
D008363
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MeSH Number(s) |
C16.320.565.202.607.500 C16.320.565.595.577.500 C18.452.648.202.607.500 C18.452.648.595.577.500
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Concept/Terms |
alpha-Mannosidosis- alpha-Mannosidosis
- alpha Mannosidosis
- alpha-Mannosidoses
- Alpha-Mannosidase B Deficiency
- Mannosidosis, alpha B, Lysosomal
- Alpha-Mannosidosis, Type I
- Lysosomal alpha-D-Mannosidase Deficiency
- Deficiencies, Lysosomal alpha-D-Mannosidase
- Deficiency, Lysosomal alpha-D-Mannosidase
- Lysosomal alpha D Mannosidase Deficiency
- Lysosomal alpha-D-Mannosidase Deficiencies
- alpha-D-Mannosidase Deficiencies, Lysosomal
- alpha-D-Mannosidase Deficiency, Lysosomal
- Mannosidosis, alpha B Lysosomal
- alpha Mannosidase B Deficiency
- alpha-Mannosidase Deficiency
- Deficiencies, alpha-Mannosidase
- Deficiency, alpha-Mannosidase
- alpha Mannosidase Deficiency
- alpha-Mannosidase Deficiencies
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Below are MeSH descriptors whose meaning is more general than "alpha-Mannosidosis".
Below are MeSH descriptors whose meaning is more specific than "alpha-Mannosidosis".
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