# autosomal dominant non-syndromic intellectual disability 29

> autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of SETBP1 on chromosome 18q12.3

**Wikidata**: [Q50349633](https://www.wikidata.org/wiki/Q50349633)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-non-syndromic-intellectual-disability-29


## References

1. Disease Ontology
2. UniProt
3. Refining analyses of copy number variation identifies specific genes associated with developmental delay
4. [Identifiers.org](https://registry.identifiers.org/registry/doid)
5. Monarch Disease Ontology release 2018-06-29