Disease & disorder
B3GALT6-related congenital disorder of glycosylation
MONDO:0100586
Any congenital disorder of glycosylation in which the cause of the disease is a mutation in B3GALT6.
Outbreak surveillance
Global reported eventsExplore recent public health notices potentially related to B3GALT6-related 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.