# White-Sutton syndrome

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

**Wikidata**: [Q50349641](https://www.wikidata.org/wiki/Q50349641)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/White–Sutton_syndrome)  
**Source**: https://4ort.xyz/entity/white-sutton-syndrome


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Large-scale discovery of novel genetic causes of developmental disorders
5. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/c5742d94-0642-4598-9fbd-fd43a2c21559--2020-03-09T16:00:00)
6. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_c5742d94-0642-4598-9fbd-fd43a2c21559-2020-03-09T160000.000Z)
7. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000143442/MONDO_0014606)
8. [Identifiers.org](https://registry.identifiers.org/registry/doid)