About Situs ambiguus
Situs ambiguus is a rare disease catalogued by Orphanet (ORPHA:157769). It is associated with the PKD1L1, ZIC3, ACVR2B 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 Situs ambiguus trials.
Search ClinicalTrials.gov for "Situs ambiguus" or filter by Orphanet code ORPHA:157769 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
Find recruiting Situs ambiguus trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Situs ambiguus. Updated daily.