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Summary Literature (0)
MIM:616721 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIn; CDG2N

Xenbase Genes: slc39a8

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014746 - SLC39A8-CDG

Disease Ontology (DO):
DOID:0070266 - congenital disorder of glycosylation type IIn