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Summary Literature (0)
MIM:611209 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G

Xenbase Genes: cog1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012637 - COG1-congenital disorder of glycosylation

Disease Ontology (DO):
DOID:0050571 - congenital disorder of glycosylation type II
DOID:0070259 - congenital disorder of glycosylation type IIg