About Autosomal recessive optic atrophy, OPA7 type
Autosomal recessive optic atrophy, OPA7 type is a rare disease catalogued by Orphanet (ORPHA:227976). It is associated with the TMEM126A 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 recessive optic atrophy, OPA7 type trials.
Search ClinicalTrials.gov for "Autosomal recessive optic atrophy, OPA7 type" or filter by Orphanet code ORPHA:227976 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
Find recruiting Autosomal recessive optic atrophy, OPA7 type trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Autosomal recessive optic atrophy, OPA7 type. Updated daily.