# autosomal dominant non-syndromic intellectual disability 21

> autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of CTCF on chromosome 16q22.1

**Wikidata**: [Q50349625](https://www.wikidata.org/wiki/Q50349625)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-non-syndromic-intellectual-disability-21


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. De novo mutations in the genome organizer CTCF cause intellectual disability.
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000102974/MONDO_0014213)
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)
7. UMLS 2023