Disease Directory Thyroid ectopia
Endocrine

Thyroid ectopia

Type

Morphological anomaly

Gene

NKX2-5, PAX8

About Thyroid ectopia

Thyroid ectopia is a rare disease catalogued by Orphanet (ORPHA:95712). It is associated with the NKX2-5, PAX8 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 Thyroid ectopia trials.

Search ClinicalTrials.gov for "Thyroid ectopia" or filter by Orphanet code ORPHA:95712 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:95712)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Thyroid ectopia trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Thyroid ectopia. Updated daily.