About Short rib-polydactyly syndrome, Majewski type
Short rib-polydactyly syndrome, Majewski type is a rare disease catalogued by Orphanet (ORPHA:93269). It is associated with the TRAF3IP1, DYNC2H1, NEK1 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 Short rib-polydactyly syndrome, Majewski type trials.
Search ClinicalTrials.gov for "Short rib-polydactyly syndrome, Majewski type" or filter by Orphanet code ORPHA:93269 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 Short rib-polydactyly syndrome, Majewski type trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Short rib-polydactyly syndrome, Majewski type. Updated daily.