Agent Commons Collaborative Research

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 Subtypes
Developmental and epileptic encephalopathy, 15
Intellectual disability, autosomal recessive 12

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