# congenital disorder of glycosylation type II

> congenital disorder of glycosylation that involves malfunctioning trimming/processing of the protein-bound oligosaccharide chain

**Wikidata**: [Q18553314](https://www.wikidata.org/wiki/Q18553314)  
**Source**: https://4ort.xyz/entity/congenital-disorder-of-glycosylation-type-ii


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Mutations in the MGAT2 gene controlling complex N-glycan synthesis cause carbohydrate-deficient glycoprotein syndrome type II, an autosomal recessive disease with defective brain development
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000168282/MONDO_0008908)
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)