Mannosidosis

From Wikipedia, the free encyclopedia

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

There are two types:

• Alpha-mannosidosis
• Beta-mannosidosis

[edit] References

v • d • e Inborn error of carbohydrate metabolism - Lysosomal storage diseases: glycoprotein metabolic pathology - Glycoproteinosis, including mucolipidosis (E77, 272.7) Post-translational modification of lysosomal enzymes I-cell disease/II - Pseudo-Hurler polydystrophy/III Glycoprotein degradation Aspartylglucosaminuria - Fucosidosis - mannosidosis (Alpha-mannosidosis, Beta-mannosidosis) - Sialidosis/I Other Mucolipidosis type IV - Salla disease - Galactosialidosis see also enzymes