|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A congenital disorder of glycosylation that involves malfunctioning trimming/processing of the protein-bound oligosaccharide chain. (Human Disease Ontology, DOID_0050571)|
|Downloads & Tools|
1 genes associated with the congenital disorder of glycosylation, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.