DDOST-CDG (CDG-Ir)

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).

NIH genetic and rare disease info[edit source]

NIH info on DDOST-CDG (CDG-Ir)

DDOST-CDG (CDG-Ir) is a rare disease.

DDOST-CDG (CDG-Ir) Resources
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Rare diseases - DDOST-CDG (CDG-Ir)
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Resources	NIH GARD, US Genetic and Rare Diseases Info Rare Disease Day Undiagnosed Diseases Network Database of rare diseases at Orphanet Rare Disease UK Rare diseases search engine