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Summary Literature (0)
MIM:607143 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig; CDG1G

Xenbase Genes: alg12

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011783 - ALG12-congenital disorder of glycosylation

Disease Ontology (DO):
DOID:0050570 - congenital disorder of glycosylation type I
DOID:0080559 - congenital disorder of glycosylation Ig