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Summary Literature (0)
MIM:601110 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D

Xenbase Genes: alg3

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010998 - ALG3-congenital disorder of glycosylation

Disease Ontology (DO):
DOID:0050570 - congenital disorder of glycosylation type I
DOID:0080556 - congenital disorder of glycosylation Id