# autosomal dominant non-syndromic intellectual disability 38

> autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of EEF1A2 on chromosome 20q13.33

**Wikidata**: [Q50349642](https://www.wikidata.org/wiki/Q50349642)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-non-syndromic-intellectual-disability-38


## References

1. Disease Ontology
2. UniProt
3. De novo EEF1A2 mutations in patients with characteristic facial features, intellectual disability, autistic behaviors and epilepsy
4. [Identifiers.org](https://registry.identifiers.org/registry/doid)
5. Monarch Disease Ontology release 2018-06-29