# Joubert syndrome 6

> Joubert syndrome that has material basis in homozygous or compound heterozygous mutation in the TMEM67 on chromosome 8q22

**Wikidata**: [Q32145884](https://www.wikidata.org/wiki/Q32145884)  
**Source**: https://4ort.xyz/entity/joubert-syndrome-6


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. [Identifiers.org](https://registry.identifiers.org/registry/doid)