Alg1-Congenital Disorder of Glycosylation, also known as congenital disorder of glycosylation type 1k, is related to congenital disorder of glycosylation, type ik and congenital disorder of glycosylation, type in. An important gene associated with Alg1-Congenital Disorder of Glycosylation is ALG1 (ALG1 Chitobiosyldiphosphodolichol Beta-Mannosyltransferase). Affiliated tissues include eye and endothelial.