alpha-Mannosidosis Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D008363
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Genes

1 genes/proteins associated with the disease alpha-Mannosidosis from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
MAN2B1 mannosidase, alpha, class 2B, member 1 2.88009