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Summary Literature (0)
MIM:617395 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIq; CDG2Q

Xenbase Genes: cog2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0054559 - congenital disorder of glycosylation, type IIq

Disease Ontology (DO):
DOID:0070269 - congenital disorder of glycosylation type IIq