About Polydactyly of a triphalangeal thumb
Polydactyly of a triphalangeal thumb is a rare disease catalogued by Orphanet (ORPHA:93336). It is associated with the SHH, LMBR1 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 Polydactyly of a triphalangeal thumb trials.
Search ClinicalTrials.gov for "Polydactyly of a triphalangeal thumb" or filter by Orphanet code ORPHA:93336 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 Polydactyly of a triphalangeal thumb trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Polydactyly of a triphalangeal thumb. Updated daily.