Congenital Disorder of Glycosylation Type Ic

A congenital disorder of glycosylation sub-type caused by mutation(s) in the ALG6 gene, encoding dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase.

Source: NCI Thesaurus (C126869).

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Congenital Disorder of Glycosylation Type Ic

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