Disease & disorder
DDOST-congenital disorder of glycosylation
MONDO:0013789
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).
Outbreak surveillance
Global reported eventsExplore recent public health notices potentially related to DDOST-congenital disorder of glycosylation. Results are keyword matches, not yet verified disease-to-outbreak relationships.
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Drugs being studied
Disease identity and terminology: MONDO. Trial relationships: ClinicalTrials.gov.