# cone-rod dystrophy 16

> cone-rod dystrophy that has material basis in homozygous or compound heterozygous mutation in the C8ORF37 gene on chromosome 8q22

**Wikidata**: [Q32146175](https://www.wikidata.org/wiki/Q32146175)  
**Source**: https://4ort.xyz/entity/cone-rod-dystrophy-16


## References

1. Disease Ontology
2. UniProt
3. Mutations in C8orf37, encoding a ciliary protein, are associated with autosomal-recessive retinal dystrophies with early macular involvement
4. [Identifiers.org](https://registry.identifiers.org/registry/doid)
5. Monarch Disease Ontology release 2018-06-29