# autosomal dominant non-syndromic intellectual disability 18

> autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of GATAD2B on chromosome 1q21.3

**Wikidata**: [Q50349622](https://www.wikidata.org/wiki/Q50349622)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-non-syndromic-intellectual-disability-18


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Diagnostic exome sequencing in persons with severe intellectual disability
5. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_5fb40641-ec79-4fee-9111-d38d2062c15b-2022-02-01T170000.000Z)
6. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000143614/MONDO_0014034)
7. [Identifiers.org](https://registry.identifiers.org/registry/doid)
8. UMLS 2023