Cog5-Congenital Disorder of Glycosylation

Cog5-Congenital Disorder of Glycosylation, also known as carbohydrate deficient glycoprotein syndrome type iii, is related to congenital disorder of glycosylation, type iii and congenital disorder of glycosylation, type in. An important gene associated with Cog5-Congenital Disorder of Glycosylation is COG5 (Component Of Oligomeric Golgi Complex 5). Affiliated tissues include liver and bone.