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Pseudohypoaldosteronism type 2C

MONDO:0013778

Any pseudohypoaldosteronism type 2 in which the cause of the disease is a mutation in the WNK1 gene.

Also known as: PHA2C, WNK1 pseudohypoaldosteronism type 2, pseudohypoaldosteronism type 2 caused by mutation in WNK1, pseudohypoaldosteronism, type 2C, pseudohypoaldosteronism, type IIC

11 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Kidney disorder (202) Hereditary disease (172) Urinary system disorder (62) Human disease (14) Pseudohypoaldosteronism (3) Disease of genetic or genomic mechanism (2) Pseudohypoaldosteronism type 2 (2) Disease by body system or component (0) Disease by etiologic mechanism (0)
Trials to join now! 5 Not yet recruiting 2 Not yet finished but already full! 3 Completed 1
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  • Sweat sensor could replace needles for kidney patients

    Diagnosis Completed

    This study tested a new wearable patch that collects sweat to measure sodium and creatinine levels, which are important for monitoring kidney health and dehydration. Five adults with kidney disease wore the patch while their sweat was analyzed using a special light-based techniqu…

    Phase: NA • Sponsor: Korea University • Aim: Diagnosis

    Last updated Jun 27, 2026 08:11 UTC

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