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Summary Literature (0)
OMIM:608779 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E


Xenbase Genes: cog7

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012118 - COG7-CDG

Disease Ontology (DO):
DOID:0050571 - congenital disorder of glycosylation type II
DOID:0070257 - congenital disorder of glycosylation type IIe