# Bardet-Biedl syndrome 19

> Bardet-Biedl syndrome that has material basis in homozygous mutation in the IFT27 gene on chromosome 22q12

**Wikidata**: [Q27674846](https://www.wikidata.org/wiki/Q27674846)  
**Source**: https://4ort.xyz/entity/bardet-biedl-syndrome-19


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. IFT27, encoding a small GTPase component of IFT particles, is mutated in a consanguineous family with Bardet-Biedl syndrome
5. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)