Disease Directory OBSOLETE: Autosomal recessive optic atrophy, OPA6 type
Rare Disease

OBSOLETE: Autosomal recessive optic atrophy, OPA6 type

Type

Clinical subtype

About OBSOLETE: Autosomal recessive optic atrophy, OPA6 type

OBSOLETE: Autosomal recessive optic atrophy, OPA6 type is a rare disease catalogued by Orphanet (ORPHA:99012). 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 OBSOLETE: Autosomal recessive optic atrophy, OPA6 type trials.

Search ClinicalTrials.gov for "OBSOLETE: Autosomal recessive optic atrophy, OPA6 type" or Orphanet code ORPHA:99012 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

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Orphanet

European reference resource for rare diseases (ORPHA:99012)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting OBSOLETE: Autosomal recessive optic atrophy, OPA6 type trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for OBSOLETE: Autosomal recessive optic atrophy, OPA6 type. Updated daily.