# Leber congenital amaurosis 17

> Leber congenital amaurosis that has material basis in mutation in the GDF6 gene on chromosome 8q22

**Wikidata**: [Q27677681](https://www.wikidata.org/wiki/Q27677681)  
**Source**: https://4ort.xyz/entity/leber-congenital-amaurosis-17


## References

1. Disease Ontology
2. UniProt
3. Contribution of growth differentiation factor 6-dependent cell survival to early-onset retinal dystrophies
4. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)
5. Monarch Disease Ontology release 2018-06-29