About Oculogastrointestinal-neurodevelopmental syndrome
Oculogastrointestinal-neurodevelopmental syndrome is a rare disease catalogued by Orphanet (ORPHA:611201). It is associated with the CAPN15 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 Oculogastrointestinal-neurodevelopmental syndrome trials.
Search ClinicalTrials.gov for "Oculogastrointestinal-neurodevelopmental syndrome" or filter by Orphanet code ORPHA:611201 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 Oculogastrointestinal-neurodevelopmental syndrome trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Oculogastrointestinal-neurodevelopmental syndrome. Updated daily.