About Familial cavitary optic disc anomaly
Familial cavitary optic disc anomaly is a rare disease catalogued by Orphanet (ORPHA:464760). It is associated with the MMP19 gene. 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 Familial cavitary optic disc anomaly trials.
Search ClinicalTrials.gov for "Familial cavitary optic disc anomaly" or filter by Orphanet code ORPHA:464760 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 Familial cavitary optic disc anomaly trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Familial cavitary optic disc anomaly. Updated daily.