# cone-rod dystrophy 3

> cone-rod dystrophy that has material basis in homozygous or compound heterozygous mutation in the ABCA4 on chromosome 1p22

**Wikidata**: [Q32146055](https://www.wikidata.org/wiki/Q32146055)  
**Source**: https://4ort.xyz/entity/cone-rod-dystrophy-3


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCR
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)