Disease Directory Coloboma of iris
Rare Disease

Coloboma of iris

Type

Morphological anomaly

Gene

ACTG1, FZD5, SALL2, ABCB6, PAX6

About Coloboma of iris

Coloboma of iris is a rare disease catalogued by Orphanet (ORPHA:98944). It is associated with the ACTG1, FZD5, SALL2 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 Coloboma of iris trials.

Search ClinicalTrials.gov for "Coloboma of iris" or filter by Orphanet code ORPHA:98944 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

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Orphanet

European reference resource for rare diseases (ORPHA:98944)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting Coloboma of iris trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Coloboma of iris. Updated daily.