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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.

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Sub-types

Liddle syndrome 1 (0) Liddle syndrome 2 (0) Liddle syndrome 3 (0)

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) Disease by body system or component (0) Disease by etiologic mechanism (0)

Trials to join now! 1 Not yet finished but already full! 1

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