Lysosomal beta-mannosidase deficiency 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 beta-A-manosidase enzyme resulting in the disruption of N-linked glycoprotein oligosaccharide catabolism. (Human Disease Ontology, DOID_3633)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C538599
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Genes

1 genes/proteins associated with the disease Lysosomal beta-mannosidase deficiency from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
MANBA mannosidase, beta A, lysosomal 2.88009