# autosomal dominant non-syndromic intellectual disability 33

> autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of DPP6 on chromosome 7q36.2

**Wikidata**: [Q50349637](https://www.wikidata.org/wiki/Q50349637)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-non-syndromic-intellectual-disability-33


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Loss-of-function variation in the DPP6 gene is associated with autosomal dominant microcephaly and mental retardation
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)