About Distal deletion 1q syndrome
Distal deletion 1q syndrome is a rare disease catalogued by Orphanet (ORPHA:36367). It is associated with the ZBTB18 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 Distal deletion 1q syndrome trials.
Search ClinicalTrials.gov for "Distal deletion 1q syndrome" or filter by Orphanet code ORPHA:36367 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 Distal deletion 1q syndrome trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Distal deletion 1q syndrome. Updated daily.