About Autosomal dominant non-syndromic intellectual disability
Autosomal dominant non-syndromic intellectual disability is a rare disease catalogued by Orphanet (ORPHA:178469). It is associated with the KCNQ2, ERBB4, BRSK2 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 Autosomal dominant non-syndromic intellectual disability trials.
Search ClinicalTrials.gov for "Autosomal dominant non-syndromic intellectual disability" or filter by Orphanet code ORPHA:178469 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 Autosomal dominant non-syndromic intellectual disability trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Autosomal dominant non-syndromic intellectual disability. Updated daily.