# cone-rod dystrophy 10

> cone-rod dystrophy that has material basis in compound heterozygous mutation in the SEMA4A gene on chromosome 1q22

**Wikidata**: [Q32146111](https://www.wikidata.org/wiki/Q32146111)  
**Source**: https://4ort.xyz/entity/cone-rod-dystrophy-10


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Identification of novel mutations in the SEMA4A gene associated with retinal degenerative diseases
5. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)