Category:Alpha-mannosidosis

**alpha-mannosidosis**
	lysosomal storage disease that has material basis in deficiency of the alpha-D-manosidase enzyme resulting in the impairment of cell function from a build up of complex sugars derived from glycoproteins in the lysosome
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Instance of	developmental defect during embryogenesis; rare disease; class of disease;
Subclass of	lysosomal storage disease; Mannosidosis; neurometabolic disease; oligosaccharidosis; rare genetic developmental defect during embryogenesis; lysosomal storage disease with skeletal involvement; metabolic disease with cataract; metabolic disease with corneal opacity; cataract associated with a metabolic disease;
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	Q250449;
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Media in category "Alpha-mannosidosis"

The following 5 files are in this category, out of 5 total.