Disease Directory Hypoplastic left heart syndrome
Rare Disease

Hypoplastic left heart syndrome

Type

Morphological anomaly

Gene

GJA1, NKX2-5

About Hypoplastic left heart syndrome

Hypoplastic left heart syndrome is a rare disease catalogued by Orphanet (ORPHA:2248). It is associated with the GJA1, NKX2-5 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 Hypoplastic left heart syndrome trials.

Search ClinicalTrials.gov for "Hypoplastic left heart syndrome" or filter by Orphanet code ORPHA:2248 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:2248)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Hypoplastic left heart syndrome trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Hypoplastic left heart syndrome. Updated daily.