# Seckel syndrome 5

> Seckel syndrome that has material basis in homozygous or compound heterozygous mutation in the CEP152 gene on chromosome 15q21

**Wikidata**: [Q50349585](https://www.wikidata.org/wiki/Q50349585)  
**Source**: https://4ort.xyz/entity/seckel-syndrome-5


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. CEP152 is a genome maintenance protein disrupted in Seckel syndrome
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)