# Leber congenital amaurosis 8

> Leber congenital amaurosis that is characterized by night blindness and thick unlaminated retinas and has material basis in mutation in the CRB1 gene on chromosome 1q31-q32

**Wikidata**: [Q27677617](https://www.wikidata.org/wiki/Q27677617)  
**Source**: https://4ort.xyz/entity/leber-congenital-amaurosis-8


## References

1. Disease Ontology
2. UniProt
3. Mutations in the CRB1 Gene Cause Leber Congenital Amaurosis
4. [Identifiers.org](https://registry.identifiers.org/registry/doid)
5. Monarch Disease Ontology release 2018-06-29