Bartter disease type 4B
MONDO:0000909A Bartter disease that has material basis in simultaneous mutation in both the CLCNKA and CLCNKB genes.
Also known as: BARTS4B, Bartter disease type 4B, Bartter syndrome, type 4B, Bartter syndrome, infantile, with sensorineural deafness, Bartter syndrome, type 4B, neonatal, with sensorineural deafness
11 clinical trials for this condition and its sub-types.
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