COG5-CDG (CDG-IIi)

Alternate names[edit | edit source]

CDG IIi; COG5-CDG (CDG-Iii). ; CDG syndrome type IIi; CDG-IIi; CDG2I; Carbohydrate deficient glycoprotein syndrome type IIi; Congenital disorder of glycosylation type IIi; CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi; COG5-CDG; Congenital disorder of glycosylation type 2i

Definition[edit | edit source]

COG5-CDG is an extremely rare form of CDG syndrome characterized clinically in the single reported case to date by moderate mental retardation with slow and inarticulate speech, truncal ataxia, and mild hypotonia.

NIH genetic and rare disease info[edit source]

NIH info on COG5-CDG (CDG-IIi)

COG5-CDG (CDG-IIi) is a rare disease.

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Also see	Comprehensive list of genetic and rare diseases
Resources	NIH GARD, US Genetic and Rare Diseases Info Rare Disease Day Undiagnosed Diseases Network Database of rare diseases at Orphanet Rare Disease UK Rare diseases search engine