# autosomal dominant non-syndromic intellectual disability 42

> autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of GNB1 on chromosome 1p36.33

**Wikidata**: [Q50349646](https://www.wikidata.org/wiki/Q50349646)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-non-syndromic-intellectual-disability-42


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and Seizures
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)