|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||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)|
|Downloads & Tools|
1 genes/proteins associated with the disease alpha-Mannosidosis from the curated CTD Gene-Disease Associations dataset.
|MAN2B1||mannosidase, alpha, class 2B, member 1||2.88009|