# Bardet-Biedl syndrome 2

> Bardet-Biedl syndrome that has material basis in homozygous or compound heterozygous mutations in the BBS2 gene on chromosome 16q13

**Wikidata**: [Q27674828](https://www.wikidata.org/wiki/Q27674828)  
**Source**: https://4ort.xyz/entity/bardet-biedl-syndrome-2


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2)
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)