About FRAXE intellectual disability
FRAXE intellectual disability is a rare disease catalogued by Orphanet (ORPHA:100973). It is associated with the AFF2, FMR3 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 FRAXE intellectual disability trials.
Search ClinicalTrials.gov for "FRAXE intellectual disability" or filter by Orphanet code ORPHA:100973 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 FRAXE intellectual disability trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for FRAXE intellectual disability. Updated daily.