# Leber congenital amaurosis 7

> Leber congenital amaurosis that has material basis in mutation in the CRX gene on chromosome 19q13

**Wikidata**: [Q27677734](https://www.wikidata.org/wiki/Q27677734)  
**Source**: https://4ort.xyz/entity/leber-congenital-amaurosis-7


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)