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Summary Literature (0)
MIM:615597 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ix; CDG1X

Xenbase Genes: stt3b

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014271 - STT3B-congenital disorder of glycosylation

Disease Ontology (DO):
DOID:0050570 - congenital disorder of glycosylation type I
DOID:0080573 - congenital disorder of glycosylation Ix