# Bartter disease type 2

> Bartter disease that has material basis in homozygous or compound heterozygous mutation in the potassium channel ROMK gene (KCNJ1) on chromosome 11q24

**Wikidata**: [Q27674848](https://www.wikidata.org/wiki/Q27674848)  
**Source**: https://4ort.xyz/entity/bartter-disease-type-2


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)