# autosomal dominant non-syndromic intellectual disability 6

> autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of GRIN2B on chromosome 12p13.1

**Wikidata**: [Q50349610](https://www.wikidata.org/wiki/Q50349610)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/GRIN2B-related_neurodevelopmental_disorder)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-non-syndromic-intellectual-disability-6


## References

1. Disease Ontology
2. UniProt
3. Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes
4. [Identifiers.org](https://registry.identifiers.org/registry/doid)
5. Monarch Disease Ontology release 2018-06-29