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Liddle syndrome

MONDO:0008323

A rare genetic form of low-renin hypertension characterized by hypertension associated with decreased plasma levels of potassium and aldosterone.

Also known as: Liddle syndrome, pseudoaldosteronism, pseudohyperaldosteronism type 1, LIDLS

2 clinical trials for this condition and its sub-types, 1 tagged with Liddle syndrome itself.

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↑ Syndromic disease (7133) ↑ Inherited kidney disorder (317) ↑ Renal tubular transport disease (17)

Sub-types of Liddle syndrome

  • Liddle syndrome 1 0 trials
  • Liddle syndrome 2 0 trials
  • Liddle syndrome 3 0 trials
Including sub-types (2) Tagged with Liddle syndrome (1)
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  • Newborn screening study aims to catch rare diseases at birth

    Diagnosis Ongoing

    This study offers voluntary screening for newborns in North Carolina to detect a wide range of rare health conditions early. Using a small blood sample already collected at birth, the program tests for dozens of disorders, including spinal muscular atrophy, cystic fibrosis, and m…

    Sponsor: RTI International • Aim: Diagnosis

    Last updated Jul 03, 2026 00:00 UTC

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