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Up to: Congenital disorder of glycosylation type I · Disorder of protein N-glycosylation
DDOST-congenital disorder of glycosylation
DDOST-CDG is a form of congenital disorders of N-linked glycosylation characterized by failure to thrive, developmental delay, hypotonia, strabismus and hepatic dysfunction. The disease is caused by mutations in the gene DDOST (1p36.1).
This condition has no sub-types.