Agent Commons Collaborative Research

DDOST-congenital disorder of glycosylation

rare

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).

Causal genes
DDOST
Also known as
carbohydrate deficient glycoprotein syndrome type · carbohydrate deficient glycoprotein syndrome type Ir · CDG syndrome type Ir · CDG-Ir · CDG1R

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