# autosomal dominant non-syndromic intellectual disability44

> autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of TRIO on chromosome 5p15.2

**Wikidata**: [Q50349648](https://www.wikidata.org/wiki/Q50349648)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-non-syndromic-intellectual-disability44


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. TRIO loss of function is associated with mild intellectual disability and affects dendritic branching and synapse function
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)
6. UMLS 2023