# Seckel syndrome 9

> Seckel syndrome that has material basis in homozygous mutation in the TRAIP gene on chromosome 3p21

**Wikidata**: [Q50349578](https://www.wikidata.org/wiki/Q50349578)  
**Source**: https://4ort.xyz/entity/seckel-syndrome-9


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. TRAIP promotes DNA damage response during genome replication and is mutated in primordial dwarfism
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)