# Greig cephalopolysyndactyly syndrome

> acrocephalosyndactylia that has material basis in mutation in the GLI3 gene which results in abnormal development located in limb, located in head, located in face

**Wikidata**: [Q3508649](https://www.wikidata.org/wiki/Q3508649)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Greig_cephalopolysyndactyly_syndrome)  
**Source**: https://4ort.xyz/entity/greig-cephalopolysyndactyly-syndrome


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000106571/MONDO_0008287)
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)