About Microphthalmia with brain and digit anomalies
Microphthalmia with brain and digit anomalies is a rare disease catalogued by Orphanet (ORPHA:139471). It is associated with the BMP4 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 brain and digit anomalies trials.
Search ClinicalTrials.gov for "Microphthalmia with brain and digit anomalies" or filter by Orphanet code ORPHA:139471 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 brain and digit anomalies trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Microphthalmia with brain and digit anomalies. Updated daily.