About Matthew-Wood syndrome
Matthew-Wood syndrome is a rare disease catalogued by Orphanet (ORPHA:2470). It is associated with the STRA6, WNT7B 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 Matthew-Wood syndrome trials.
Search ClinicalTrials.gov for "Matthew-Wood syndrome" or filter by Orphanet code ORPHA:2470 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 Matthew-Wood syndrome trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Matthew-Wood syndrome. Updated daily.