About Congenital stationary night blindness, Riggs type
Congenital stationary night blindness, Riggs type is a rare disease catalogued by Orphanet (ORPHA:714096). It is associated with the GNAT1, PDE6B 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 Congenital stationary night blindness, Riggs type trials.
Search ClinicalTrials.gov for "Congenital stationary night blindness, Riggs type" or filter by Orphanet code ORPHA:714096 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 Congenital stationary night blindness, Riggs type trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Congenital stationary night blindness, Riggs type. Updated daily.