# Leber congenital amaurosis 13

> Human disease

**Wikidata**: [Q27677730](https://www.wikidata.org/wiki/Q27677730)  
**Source**: https://4ort.xyz/entity/leber-congenital-amaurosis-13


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause childhood-onset severe retinal dystrophy
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)