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Diseases / Metabolic disease/ Inborn errors of metabolism/ Congenital disorder of glycosylation/ Disorder of protein N-glycosylation

ST3GAL3-congenital disorder of glycosylation

rare

Identifiers: MONDO:0979317 Orphanet:697734
Causal genes: ST3GAL3
Part of: Disorder of protein N-glycosylation
Also known as: ST3GAL3-CDG

Subtypes

All diseases Rare only

Disease

Developmental and epileptic encephalopathy, 15 MONDO:0014003
Intellectual disability, autosomal recessive 12 MONDO:0012612

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