Congenital Disorder of Glycosylation Type Ig

**Semantic type:** Disease or Syndrome

**Definition:** A congenital disorder of glycosylation sub-type caused by mutation(s) in the ALG12 gene, dol-P-Man:Man(7)GlcNAc(2)-PP-Dol alpha-1,6-mannosyltransferase.

**Synonyms:** - CDGIg