Congenital Disorder of Glycosylation Type Ic

**Semantic type:** Disease or Syndrome

**Definition:** A congenital disorder of glycosylation sub-type caused by mutation(s) in the ALG6 gene, encoding dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase.

**Synonyms:** - CDGIc