Congenital disorder of glycosylation type II Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A congenital disorder of glycosylation that involves malfunctioning trimming/processing of the protein-bound oligosaccharide chain. (Human Disease Ontology, DOID_0050571)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C535747
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Genes

1 genes/proteins associated with the disease Congenital disorder of glycosylation type II from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
ALG2 ALG2, alpha-1,3/1,6-mannosyltransferase 2.88009