About Rare isolated myopia
Rare isolated myopia is a rare disease catalogued by Orphanet (ORPHA:98619). It is associated with the SLC39A5, SCO2, P3H2 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 Rare isolated myopia trials.
Search ClinicalTrials.gov for "Rare isolated myopia" or filter by Orphanet code ORPHA:98619 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 Rare isolated myopia trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Rare isolated myopia. Updated daily.