# atypical glycine encephalopathy

> Atypical glycine encephalopathy is a rare form of glycine encephalopathy (GE; see this term) presenting disease onset or clinical manifestations that differ from neonatal or infantile GE

**Wikidata**: [Q55785179](https://www.wikidata.org/wiki/Q55785179)  
**Source**: https://4ort.xyz/entity/atypical-glycine-encephalopathy


## References

1. Monarch Disease Ontology release 2018-06-29
2. Mutation in SLC6A9 encoding a glycine transporter causes a novel form of non-ketotic hyperglycinemia in humans
3. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000196517/MONDO_0015010)
4. UMLS 2023