# Joubert syndrome 20

> Joubert syndrome that has material basis in compound heterozygous mutation in the TMEM231 gene on chromosome 16q23

**Wikidata**: [Q32145716](https://www.wikidata.org/wiki/Q32145716)  
**Source**: https://4ort.xyz/entity/joubert-syndrome-20


## References

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