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Summary Literature (0)
MIM:612379 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iq; CDG1Q

Xenbase Genes: srd5a3

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012885 - SRD5A3-congenital disorder of glycosylation

Disease Ontology (DO):
DOID:0050570 - congenital disorder of glycosylation type I
DOID:0080568 - congenital disorder of glycosylation Iq