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. (Human Disease Ontology, DOID_3413)
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Genes
1 genes involed in the disease alpha-mannosidosis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
