Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:612015 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE In; CDG1N

Xenbase Genes: rtf1, rft1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012783 - RFT1-congenital disorder of glycosylation

Disease Ontology (DO):
DOID:0050570 - congenital disorder of glycosylation type I
DOID:0080566 - congenital disorder of glycosylation In