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Summary Literature (0)
MIM:615596 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw, AUTOSOMAL RECESSIVE; CDG1WAR

Xenbase Genes: stt3a

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014270 - STT3A-congenital disorder of glycosylation

Disease Ontology (DO):
DOID:0050570 - congenital disorder of glycosylation type I
DOID:0080572 - congenital disorder of glycosylation Iw