# Seckel syndrome 8

> Seckel syndrome that has material basis in homozygous mutation in the DNA2 gene on chromosome 10q21

**Wikidata**: [Q50349582](https://www.wikidata.org/wiki/Q50349582)  
**Source**: https://4ort.xyz/entity/seckel-syndrome-8


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Genomic analysis of primordial dwarfism reveals novel disease genes
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)