About Benign hereditary chorea
Benign hereditary chorea is a rare disease catalogued by Orphanet (ORPHA:1429). It is associated with the NKX2-1, ADCY5 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 Benign hereditary chorea trials.
Search ClinicalTrials.gov for "Benign hereditary chorea" or filter by Orphanet code ORPHA:1429 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 Benign hereditary chorea trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Benign hereditary chorea. Updated daily.