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Summary Literature (0)
MIM:615042 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu; CDG1U

Xenbase Genes: dpm2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014023 - congenital muscular dystrophy with intellectual disability and severe epilepsy

Disease Ontology (DO):
DOID:0050570 - congenital disorder of glycosylation type I
DOID:0080571 - congenital disorder of glycosylation Iu