Disease Directory Best vitelliform macular dystrophy
Ophthalmological

Best vitelliform macular dystrophy

Type

Disease

Gene

BEST1

About Best vitelliform macular dystrophy

Best vitelliform macular dystrophy is a rare disease catalogued by Orphanet (ORPHA:1243). It is associated with the BEST1 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 Best vitelliform macular dystrophy trials.

Search ClinicalTrials.gov for "Best vitelliform macular dystrophy" or filter by Orphanet code ORPHA:1243 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:1243)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Best vitelliform macular dystrophy trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Best vitelliform macular dystrophy. Updated daily.