obsolete_COG1-CDG true OMIM:611209 ICD10:E77.8 CDG-IIg 3.41.0 Replaced with Mondo term. orphanet Congenital disorder of glycosylation type IIg CDG syndrome type IIg Congenital disorder of glycosylation type IIg (CDG-IIg) is an extremely rare form of CDG syndrome (see this term) characterized clinically in the few cases reported to date by variable signs including microcephaly, growth retardation, psychomotor retardation, and variable facial dysmorphism. Carbohydrate deficient glycoprotein syndrome type IIg http://purl.obolibrary.org/obo/MONDO_0012637 CDG2G