Mannosidosis

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

There are two types:

[edit] See also

Swainsonine

[edit] References

^ MeSH Mannosidosis

This medical article is a stub. You can help Wikipedia by expanding it.

(LSD) Inborn error of carbohydrate metabolism: glycoproteinosis (E77, 271.8)

Anabolism

Dolichol kinase deficiency · Congenital disorder of glycosylation

Post-translational modification
of lysosomal enzymes

Mucolipidosis: I-cell disease/II · Pseudo-Hurler polydystrophy/III

Catabolism

Aspartylglucosaminuria · Fucosidosis · mannosidosis (Alpha-mannosidosis, Beta-mannosidosis) · Sialidosis · Schindler disease

Other

solute carrier family (Salla disease) · Galactosialidosis

mt, k, c/g/r/p/y/i, f/h/s/l/o/e, a/u, n, m

k, cgrp/y/i, f/h/s/l/o/e, au, n, m, epon

m(A16/C10),i(k, c/g/r/p/y/i, f/h/s/o/e, a/u, n, m)

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