# autosomal dominant non-syndromic intellectual disability 26

> autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of AUTS2 on chromosome 7q11.22

**Wikidata**: [Q50349630](https://www.wikidata.org/wiki/Q50349630)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-non-syndromic-intellectual-disability-26


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000158321/MONDO_0014361)
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)
7. UMLS 2023