CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=OMIM:613661
Similar Terms
Downloads & Tools

Genes

1 genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
ALG11 ALG11, alpha-1,2-mannosyltransferase 2.88009