# cone-rod dystrophy 2

> cone-rod dystrophy that has material basis in heterozygous mutation in the CRX gene on chromosome 19q13

**Wikidata**: [Q32145936](https://www.wikidata.org/wiki/Q32145936)  
**Source**: https://4ort.xyz/entity/cone-rod-dystrophy-2


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor
5. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)