# iridogoniodysgenesis syndrome

> Human disease

**Wikidata**: [Q17125601](https://www.wikidata.org/wiki/Q17125601)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Iridogoniodysgenesis,_dominant_type)  
**Source**: https://4ort.xyz/entity/iridogoniodysgenesis-syndrome


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Autosomal dominant iris hypoplasia is caused by a mutation in the rieger syndrome (rieg/pitx2) gene
5. The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)
7. UMLS 2023