Disease Directory Hereditary optic neuropathy
Rare Disease

Hereditary optic neuropathy

Type

Category

About Hereditary optic neuropathy

Hereditary optic neuropathy is a rare disease catalogued by Orphanet (ORPHA:98671). 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 worldwide.

Clinical Trial Eligibility Tips

What to know before applying to Hereditary optic neuropathy trials.

Search ClinicalTrials.gov for "Hereditary optic neuropathy" or Orphanet code ORPHA:98671 to find disease-specific recruiting studies.

Ask your specialist to refer you to an Orphanet-accredited Centre of Expertise for this condition.

Natural history studies and patient registries often open enrolment before drug trials — contact the Orphanet patient community first.

Patient Resources

Patient Organization

Orphanet

Visit website ↗

Orphanet

European reference resource for rare diseases (ORPHA:98671)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Hereditary optic neuropathy trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Hereditary optic neuropathy. Updated daily.