About Microphthalmia with limb anomalies
Microphthalmia with limb anomalies is a rare disease catalogued by Orphanet (ORPHA:1106). It is associated with the SMOC1 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 Microphthalmia with limb anomalies trials.
Search ClinicalTrials.gov for "Microphthalmia with limb anomalies" or filter by Orphanet code ORPHA:1106 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 Microphthalmia with limb anomalies trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Microphthalmia with limb anomalies. Updated daily.