Mannosidosis

Mannosidosis is a deficiency in mannosidase, an enzyme.[1]

There are two types:

References

Mannosidosis at the US National Library of Medicine Medical Subject Headings (MeSH)

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Lysosomal storage diseases: Inborn errors of carbohydrate metabolism (Glycoproteinoses) (E77, 271.8)
Anabolism	Dolichol kinase deficiency Congenital disorder of glycosylation
Post-translational modification of lysosomal enzymes	Mucolipidosis: I-cell disease (ML II) Pseudo-Hurler polydystrophy (ML III)
Catabolism	Aspartylglucosaminuria Fucosidosis mannosidosis Alpha-mannosidosis Beta-mannosidosis Sialidosis Schindler disease
Other	solute carrier family (Salla disease) Galactosialidosis