Human genes for alpha-mannosidosis
Alpha-mannosidosis [DOID:3413]
A 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.
Synonyms: alpha-mannosidosis, alphamannosidosis, alpha-mannosidosises, DOID:3413, Alpha-D-mannosidosis ...
Linkouts: OMIM