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Bartter disease type 5

MONDO:0010503

Any Bartter syndrome in which the cause of the disease is a mutation in the MAGED2 gene.

Also known as: BARTS5, Bartter syndrome caused by mutation in MAGED2, Bartter syndrome, type 5, antenatal, transient, Bartter syndrome, type 5, antenatal, transient, X-linked recessive, MAGED2 Bartter syndrome

1 clinical trial for this condition and its sub-types.

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Broader categories

Disease (680) Kidney disorder (214) Hereditary disease (176) Urinary system disorder (66) Syndromic disease (25) Human disease (14) Disease of genetic or genomic mechanism (2) Inherited kidney disorder (1) Renal tubule disorder (1) Bartter syndrome (0)
Trials to join now! 1
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  • Could a diabetes drug protect kidneys in children with genetic disease?

    Disease control Recruiting now

    This study tests whether adding dapagliflozin (a diabetes drug) to standard care reduces protein leakage in the urine of children with hereditary kidney diseases. About 44 children will receive either dapagliflozin plus standard care or standard care alone for 12 weeks, then swit…

    Phase: PHASE3 • Sponsor: Children's Hospital of Fudan University • Aim: Disease control

    Last updated Jul 08, 2026 00:00 UTC

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