# cone-rod dystrophy 12

> cone-rod dystrophy that has material basis in homozygous or heterozygous mutation in the PROM1 gene on chromosome 4p15

**Wikidata**: [Q32146137](https://www.wikidata.org/wiki/Q32146137)  
**Source**: https://4ort.xyz/entity/cone-rod-dystrophy-12


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)