Disease Directory Isolated aniridia
Rare Disease

Isolated aniridia

Type

Morphological anomaly

Gene

PAX6, TRIM44, FOXC1

About Isolated aniridia

Isolated aniridia is a rare disease catalogued by Orphanet (ORPHA:250923). It is associated with the PAX6, TRIM44, FOXC1 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 Isolated aniridia trials.

Search ClinicalTrials.gov for "Isolated aniridia" or filter by Orphanet code ORPHA:250923 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:250923)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Isolated aniridia trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Isolated aniridia. Updated daily.