# cone-rod dystrophy 9

> cone-rod dystrophy that has material basis in homozygous or compound heterozygous mutation in the ADAM9 gene on chromosome 8p11

**Wikidata**: [Q32146150](https://www.wikidata.org/wiki/Q32146150)  
**Source**: https://4ort.xyz/entity/cone-rod-dystrophy-9


## References

1. Disease Ontology
2. UniProt
3. Loss of the metalloprotease ADAM9 leads to cone-rod dystrophy in humans and retinal degeneration in mice
4. [Identifiers.org](https://registry.identifiers.org/registry/doid)
5. Monarch Disease Ontology release 2018-06-29