# Seckel syndrome 6

> Seckel syndrome that has material basis in homozygous mutation in the CEP63 gene on chromosome 3q22

**Wikidata**: [Q50349579](https://www.wikidata.org/wiki/Q50349579)  
**Source**: https://4ort.xyz/entity/seckel-syndrome-6


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. A primary microcephaly protein complex forms a ring around parental centrioles.
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)