# Leber congenital amaurosis 2

> Leber congenital amaurosis that is characterized by night blindness, some transient improvement in vision, and eventual progressive visual loss and has material basis in mutation in the RPE65 gene on chromosome 1

**Wikidata**: [Q27677590](https://www.wikidata.org/wiki/Q27677590)  
**Source**: https://4ort.xyz/entity/leber-congenital-amaurosis-2


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations in RPE65 cause Leber's congenital amaurosis
5. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)