# Bardet-Biedl syndrome 18

> Bardet-Biedl syndrome that has material basis in homozygous mutation in the BBIP1 gene on chromosome 10q25

**Wikidata**: [Q27674845](https://www.wikidata.org/wiki/Q27674845)  
**Source**: https://4ort.xyz/entity/bardet-biedl-syndrome-18


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Exome sequencing of Bardet–Biedl syndrome patient identifies a null mutation in the BBSome subunit BBIP1 (BBS18)
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)