# autosomal dominant non-syndromic intellectual disability 7

> autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of DYRK1A on chromosome 21q22.13

**Wikidata**: [Q50349611](https://www.wikidata.org/wiki/Q50349611)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-non-syndromic-intellectual-disability-7


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Intragenic deletion in DYRK1A leads to mental retardation and primary microcephaly.
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000157540/MONDO_0013578)
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)