Disease & disorder

COG4-congenital disorder of glycosylation

MONDO:0013281

COG4-CDG is an extremely rare form of CDG syndrome characterized clinically in the single reported case to date by seizures, some dysmorphic features, axial hyponia, slight peripheral hypertonia and hyperreflexia.

Outbreak surveillance

Global reported events

Explore recent public health notices potentially related to COG4-congenital disorder of glycosylation. Results are keyword matches, not yet verified disease-to-outbreak relationships.

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Clinical trials0

Recruiting0

Drug concepts studied0

Synonyms11

Drugs being studied

Disease identity and terminology: MONDO. Trial relationships: ClinicalTrials.gov.