Disease Directory Autosomal recessive isolated optic atrophy
Rare Disease

Autosomal recessive isolated optic atrophy

Type

Disease

Gene

YME1L1, MECR, ACO2, RTN4IP1, MCAT

About Autosomal recessive isolated optic atrophy

Autosomal recessive isolated optic atrophy is a rare disease catalogued by Orphanet (ORPHA:98676). It is associated with the YME1L1, MECR, ACO2 genes. 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 recessive isolated optic atrophy trials.

Search ClinicalTrials.gov for "Autosomal recessive isolated optic atrophy" or filter by Orphanet code ORPHA:98676 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

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Orphanet

European reference resource for rare diseases (ORPHA:98676)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting Autosomal recessive isolated optic atrophy trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Autosomal recessive isolated optic atrophy. Updated daily.