# Newfoundland cone-rod dystrophy

> cone-rod dystrophy that has material basis in homozygous or compound heterozygous mutation in the RLBP1 gene on chromosome 15q26

**Wikidata**: [Q32146085](https://www.wikidata.org/wiki/Q32146085)  
**Source**: https://4ort.xyz/entity/newfoundland-cone-rod-dystrophy


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Newfoundland rod-cone dystrophy, an early-onset retinal dystrophy, is caused by splice-junction mutations in RLBP1
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)