# Seckel syndrome 7

> Seckel syndrome that has material basis in compound heterozygous mutation in the NIN gene on chromosome 14q22

**Wikidata**: [Q50349584](https://www.wikidata.org/wiki/Q50349584)  
**Source**: https://4ort.xyz/entity/seckel-syndrome-7


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Novel microcephalic primordial dwarfism disorder associated with variants in the centrosomal protein ninein
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)
6. UMLS 2023