obsolete_COG5-CDG true orphanet Carbohydrate deficient glycoprotein syndrome type IIi Replaced with Mondo term. Congenital disorder of glycosylation type IIi (CDG-IIi) is an extremely rare form of CDG syndrome (see this term) characterized clinically in the single reported case to date by moderate mental retardation with slow and inarticulate speech, truncal ataxia, and mild hypotonia. http://purl.obolibrary.org/obo/MONDO_0013325 Congenital disorder of glycosylation type IIi OMIM:613612 CDG syndrome type IIi CDG2I 3.41.0 ICD10:E77.8 CDG-IIi