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Medical Definition of Mannosidosis
1. Inborn error of metabolism marked by a defect in alpha-mannosidase activity that results in lysosomal accumulation of mannose-rich substrates. Virtually all patients have psychomotor retardation, facial coarsening, and some degree of dysostosis multiplex. It is thought to be an autosomal recessive disorder. (12 Dec 1998)
Lexicographical Neighbors of Mannosidosis
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