# Bartter disease type 3

> Bartter disease that has material basis in homozygous or compound heterozygous mutation in the kidney chloride channel B gene (CLCNKB) on chromosome 1p36

**Wikidata**: [Q27674849](https://www.wikidata.org/wiki/Q27674849)  
**Source**: https://4ort.xyz/entity/bartter-disease-type-3


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000184908/MONDO_0011822)
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)