Disease Directory Liddle syndrome
Rare Disease

Liddle syndrome

Type

Disease

Gene

SCNN1B, SCNN1G, SCNN1A

About Liddle syndrome

Liddle syndrome is a rare disease catalogued by Orphanet (ORPHA:526). It is associated with the SCNN1B, SCNN1G, SCNN1A genes. Search below for active recruiting clinical trials from ClinicalTrials.gov, or visit the Orphanet expert page for specialist centres, natural history studies, and patient registries.

Clinical Trial Eligibility Tips

What to know before applying to Liddle syndrome trials.

Search ClinicalTrials.gov for "Liddle syndrome" or filter by Orphanet code ORPHA:526 to find disease-specific studies.

Ask your specialist to refer you to a Centre of Expertise — Orphanet lists all accredited centres for this condition worldwide.

Natural history studies and patient registries often enrol before drug trials open — contact the Orphanet patient community first.

Patient Resources

Patient Organization

Orphanet

Visit website ↗

Orphanet

European reference resource for rare diseases (ORPHA:526)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Liddle syndrome trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Liddle syndrome. Updated daily.