# Leber congenital amaurosis 3

> Leber congenital amaurosis that has material basis in mutation in the SPATA7 gene on chromosome 14q31

**Wikidata**: [Q27677732](https://www.wikidata.org/wiki/Q27677732)  
**Source**: https://4ort.xyz/entity/leber-congenital-amaurosis-3


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations in SPATA7 Cause Leber Congenital Amaurosis and Juvenile Retinitis Pigmentosa
5. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)