# autosomal dominant non-syndromic intellectual disability 8

> autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of GRIN1 on chromosome 9q34.3

**Wikidata**: [Q50349612](https://www.wikidata.org/wiki/Q50349612)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-non-syndromic-intellectual-disability-8


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000176884/MONDO_0013655)
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)