# autosomal dominant non-syndromic intellectual disability 32

> autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of KAT6A on chromosome 8p11.21

**Wikidata**: [Q50349636](https://www.wikidata.org/wiki/Q50349636)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Autosomal_dominant_intellectual_disability-craniofacial_anomalies-cardiac_defects_syndrome)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-non-syndromic-intellectual-disability-32


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. De novo nonsense mutations in KAT6A, a lysine acetyl-transferase gene, cause a syndrome including microcephaly and global developmental delay
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)