Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:616828 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIo; CDG2O

Xenbase Genes: vma22

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014789 - CCDC115-CDG

Disease Ontology (DO):
DOID:0070267 - congenital disorder of glycosylation type IIo