Disease Directory Autosomal dominant optic atrophy plus syndrome
Rare Disease

Autosomal dominant optic atrophy plus syndrome

Type

Disease

Gene

OPA1

About Autosomal dominant optic atrophy plus syndrome

Autosomal dominant optic atrophy plus syndrome is a rare disease catalogued by Orphanet (ORPHA:1215). It is associated with the OPA1 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 Autosomal dominant optic atrophy plus syndrome trials.

Search ClinicalTrials.gov for "Autosomal dominant optic atrophy plus syndrome" or filter by Orphanet code ORPHA:1215 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:1215)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Autosomal dominant optic atrophy plus syndrome trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Autosomal dominant optic atrophy plus syndrome. Updated daily.