ST3GAL3-congenital disorder of glycosylation

Findings

No curated finding names ST3GAL3-congenital disorder of glycosylation yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Where it sits

A kind of

• disorder of protein N-glycosylation

Narrower terms (2)

• developmental and epileptic encephalopathy, 15
• intellectual disability, autosomal recessive 12

Resolves to: ST3GAL3-congenital disorder of glycosylation

Also called

ST3GAL3-CDG