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Summary Literature (0)
MIM:613612 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi; CDG2I

Xenbase Genes: cog5

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013325 - COG5-congenital disorder of glycosylation

Disease Ontology (DO):
DOID:0050571 - congenital disorder of glycosylation type II
DOID:0070261 - congenital disorder of glycosylation type IIi