Disease Directory Congenitally uncorrected transposition of the great arteries
Rare Disease

Congenitally uncorrected transposition of the great arteries

Type

Morphological anomaly

About Congenitally uncorrected transposition of the great arteries

Congenitally uncorrected transposition of the great arteries is a rare disease catalogued by Orphanet (ORPHA:860). 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 worldwide.

Clinical Trial Eligibility Tips

What to know before applying to Congenitally uncorrected transposition of the great arteries trials.

Search ClinicalTrials.gov for "Congenitally uncorrected transposition of the great arteries" or Orphanet code ORPHA:860 to find disease-specific recruiting studies.

Ask your specialist to refer you to an Orphanet-accredited Centre of Expertise for this condition.

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

Patient Resources

Patient Organization

Orphanet

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Orphanet

European reference resource for rare diseases (ORPHA:860)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting Congenitally uncorrected transposition of the great arteries trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Congenitally uncorrected transposition of the great arteries. Updated daily.