# Leber congenital amaurosis 16

> Leber congenital amaurosis that has material basis in mutation in the KCNJ13 gene on chromosome 2q37

**Wikidata**: [Q27677637](https://www.wikidata.org/wiki/Q27677637)  
**Source**: https://4ort.xyz/entity/leber-congenital-amaurosis-16


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Recessive mutations in KCNJ13, encoding an inwardly rectifying potassium channel subunit, cause leber congenital amaurosis
5. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)