Congenital disorder of glycosylation type II

MONDO:0005501

A congenital disorder of glycosylation that involves malfunctioning trimming/processing of the protein-bound oligosaccharide chain.

Also known as: congenital disorder of glycosylation type II, congenital disorders of glycosylation, type II, B4GALT1-CDG, B4GALT1-CDG (CDG-2d), MGAT2-CDG, MGAT2-CDG (CDG-2a), MOGS-CDG, MOGS-CDG (CDG-2b)

3 clinical trials for this condition and its sub-types, 0 tagged with Congenital disorder of glycosylation type II itself.

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