# Axenfeld-Rieger syndrome type 3

> Axenfeld-Rieger syndrome that has material basis in heterozygous mutation in the FOXC1 gene on chromosome 6p25

**Wikidata**: [Q27164456](https://www.wikidata.org/wiki/Q27164456)  
**Source**: https://4ort.xyz/entity/axenfeld-rieger-syndrome-type-3


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations of the Forkhead/Winged-Helix Gene, FKHL7, in Patients with Axenfeld-Rieger Anomaly
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)