Bartter disease type 4B

MONDO:0000909

A 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

1 clinical trial for this condition and its sub-types, 0 tagged with Bartter disease type 4B itself.

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↑ Bartter syndrome type 4 (0)

Including sub-types (1) Tagged with Bartter disease type 4B (0)

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