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Summary Literature (0)
MIM:613661 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip; CDG1P

Xenbase Genes: alg11

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013349 - ALG11-congenital disorder of glycosylation

Disease Ontology (DO):
DOID:0050570 - congenital disorder of glycosylation type I
DOID:0080567 - congenital disorder of glycosylation Ip