Disease & disorder
COG8-congenital disorder of glycosylation
MONDO:0012635
The CDG (Congenital Disorders of Glycosylation) syndromes are a group of autosomal recessive disorders affecting glycoprotein synthesis. CDG syndrome type IIh is characterized by severe psychomotor retardation, failure to thrive and intolerance to wheat and dairy products.
Outbreak surveillance
Global reported eventsExplore recent public health notices potentially related to COG8-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.