Congenital Disorder of Glycosylation Type Id

**Semantic type:** Disease or Syndrome

**Definition:** A congenital disorder of glycosylation subtype caused by mutation(s) in the ALG3 gene, encoding dol-P-Man:Man(5)GlcNAc(2)-PP-Dol alpha-1,3-mannosyltransferase.

**Synonyms:** - CDGId