Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Echinobase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Echinobase
Summary Literature (0)
MIM:611209 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G


Echinobase Genes: cog1

Human Disease Resource: OMIM


Disease Ontology (DO):
DOID:0050571 - congenital disorder of glycosylation type II