# Joubert syndrome 18

> Joubert syndrome that has material basis in homozygous mutation in the TCTN3 gene on chromosome 10q24

**Wikidata**: [Q32145685](https://www.wikidata.org/wiki/Q32145685)  
**Source**: https://4ort.xyz/entity/joubert-syndrome-18


## References

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