# cone-rod dystrophy 15

> cone-rod dystrophy that has material basis in homozygous mutation in the CDHR1 gene on chromosome 10q23

**Wikidata**: [Q32146163](https://www.wikidata.org/wiki/Q32146163)  
**Source**: https://4ort.xyz/entity/cone-rod-dystrophy-15


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations in PCDH21 cause autosomal recessive cone-rod dystrophy
5. Biallelic mutation of protocadherin-21 (PCDH21) causes retinal degeneration in humans
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)