ALG14-congenital disorder of glycosylation
MONDO:0100559Mondo
Findings
No curated finding names ALG14-congenital disorder of glycosylation yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Deficiency in the ALG14 enzyme results in incomplete assembly of the lipid linked oligosaccharide (LLO), leading to insufficient N-glycosylation of glycoproteins.
Definition from the Mondo Disease Ontology (MONDO:0100559), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
Other names
1 name
Resolves to: ALG14-congenital disorder of glycosylation
- Also called
- ALG14-CDG