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Bartter disease type 4B
rareA Bartter disease that has material basis in simultaneous mutation in both the CLCNKA and CLCNKB genes.
- Identifiers
- MONDO:0000909 OMIM:613090
- Part of
- Bartter syndrome type 4
- Also known as
- BARTS4B · Bartter syndrome, type 4B
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