# autosomal dominant non-syndromic intellectual disability 11

> autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of EPB41L1 on chromosome 20q11.23

**Wikidata**: [Q50349615](https://www.wikidata.org/wiki/Q50349615)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-non-syndromic-intellectual-disability-11


## References

1. Disease Ontology
2. UniProt
3. Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability
4. [Identifiers.org](https://registry.identifiers.org/registry/doid)
5. Monarch Disease Ontology release 2018-06-29