Disease Directory Common arterial trunk
Rare Disease

Common arterial trunk

Type

Morphological anomaly

Gene

NKX2-6, PLXND1

About Common arterial trunk

Common arterial trunk is a rare disease catalogued by Orphanet (ORPHA:3384). It is associated with the NKX2-6, PLXND1 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 Common arterial trunk trials.

Search ClinicalTrials.gov for "Common arterial trunk" or filter by Orphanet code ORPHA:3384 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:3384)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Common arterial trunk trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Common arterial trunk. Updated daily.