About Paternal uniparental disomy of chromosome 6 syndrome
Paternal uniparental disomy of chromosome 6 syndrome is a rare disease catalogued by Orphanet (ORPHA:96191). It is associated with the HYMAI, PLAGL1 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 Paternal uniparental disomy of chromosome 6 syndrome trials.
Search ClinicalTrials.gov for "Paternal uniparental disomy of chromosome 6 syndrome" or filter by Orphanet code ORPHA:96191 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 Paternal uniparental disomy of chromosome 6 syndrome trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Paternal uniparental disomy of chromosome 6 syndrome. Updated daily.