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Pseudohypoaldosteronism, type IB1, autosomal recessive

MONDO:0009917

Generalized pseudohypoaldosteronism type 1 (generalized PHA1) is a severe form of primary mineralocorticoid resistance with systemic involvement and salt loss in multiple organs.

Also known as: PHA1B, autosomal recessive PHA 1, autosomal recessive pseudohypoaldosteronism type 1, generalised PHA1, generalised pseudohypoaldosteronism type 1, generalized PHA1, generalized pseudohypoaldosteronism type 1, PHA I, autosomal recessive

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 1 (1) Renal tubule disorder (1) Disease by body system or component (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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