About Phocomelia, Schinzel type
Phocomelia, Schinzel type is a rare disease catalogued by Orphanet (ORPHA:2879). It is associated with the WNT7A 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 Phocomelia, Schinzel type trials.
Search ClinicalTrials.gov for "Phocomelia, Schinzel type" or filter by Orphanet code ORPHA:2879 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 Phocomelia, Schinzel type trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Phocomelia, Schinzel type. Updated daily.