# Ritscher-Schinzel syndrome 2

> Ritscher-Schinzel syndrome that has material basis in mutation in the CCDC22 gene on chromosome Xp11

**Wikidata**: [Q26492787](https://www.wikidata.org/wiki/Q26492787)  
**Source**: https://4ort.xyz/entity/ritscher-schinzel-syndrome-2


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. CCDC22: a novel candidate gene for syndromic X-linked intellectual disability
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000164961/Orphanet_7)
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)