# cone-rod dystrophy 19

> cone-rod dystrophy that has material basis in homozygous or compound heterozygous mutation in the TTLL5 gene on chromosome 14q24

**Wikidata**: [Q32146216](https://www.wikidata.org/wiki/Q32146216)  
**Source**: https://4ort.xyz/entity/cone-rod-dystrophy-19


## References

1. Disease Ontology
2. UniProt
3. Biallelic variants in TTLL5, encoding a tubulin glutamylase, cause retinal dystrophy
4. [Identifiers.org](https://registry.identifiers.org/registry/doid)
5. Monarch Disease Ontology release 2018-06-29