About Aniridia-cerebellar ataxia-intellectual disability syndrome
Aniridia-cerebellar ataxia-intellectual disability syndrome is a rare disease catalogued by Orphanet (ORPHA:1065). It is associated with the ITPR1, PAX6 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 Aniridia-cerebellar ataxia-intellectual disability syndrome trials.
Search ClinicalTrials.gov for "Aniridia-cerebellar ataxia-intellectual disability syndrome" or filter by Orphanet code ORPHA:1065 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 Aniridia-cerebellar ataxia-intellectual disability syndrome trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Aniridia-cerebellar ataxia-intellectual disability syndrome. Updated daily.