# Bardet-Biedl syndrome 16

> Bardet-Biedl syndrome that has material basis in homozygous or compound heterozygous mutations in the SDCCAG8 gene on chromosome 1q43

**Wikidata**: [Q27674842](https://www.wikidata.org/wiki/Q27674842)  
**Source**: https://4ort.xyz/entity/bardet-biedl-syndrome-16


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)