# Seckel syndrome

> autosomal recessive disease characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability

**Wikidata**: [Q572169](https://www.wikidata.org/wiki/Q572169)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Seckel_syndrome)  
**Source**: https://4ort.xyz/entity/seckel-syndrome


## References

1. Disease Ontology
2. Freebase Data Dumps. 2013
3. A splicing mutation affecting expression of ataxia-telangiectasia and Rad3-related protein (ATR) results in Seckel syndrome
4. [Identifiers.org](https://registry.identifiers.org/registry/doid)