Bartter disease type 4b (Q27674852)
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Bartter disease that has material basis in simultaneous mutation in both the CLCNKA and CLCNKB genes
- BARTS4B
- Bartter syndrome, type 4b, digenic
- neonatal Bartter syndrome type 4B with sensorineural deafness
- BARTTER SYNDROME, TYPE 4B
- Bartter Syndrome, Infantile, With Sensorineural Deafness
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Bartter disease type 4b |
Bartter disease that has material basis in simultaneous mutation in both the CLCNKA and CLCNKB genes |
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