# Leber congenital amaurosis 9

> Leber congenital amaurosis that has material basis in mutation in the NMNAT1 gene on chromosome 1p36

**Wikidata**: [Q27677581](https://www.wikidata.org/wiki/Q27677581)  
**Source**: https://4ort.xyz/entity/leber-congenital-amaurosis-9


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)