Congenital Disorder of Glycosylation Type Ij

**Semantic type:** Disease or Syndrome

**Definition:** A congenital disorder of glycosylation sub-type caused by mutation(s) in the DPAGT1 gene, encoding UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase.

**Synonyms:** - CDGIj