Disease Directory Third branchial cleft anomaly
Rare Disease

Third branchial cleft anomaly

Type

Morphological anomaly

About Third branchial cleft anomaly

Third branchial cleft anomaly is a rare disease catalogued by Orphanet (ORPHA:141030). 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 Third branchial cleft anomaly trials.

Search ClinicalTrials.gov for "Third branchial cleft anomaly" or Orphanet code ORPHA:141030 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:141030)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting Third branchial cleft anomaly trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Third branchial cleft anomaly. Updated daily.