congenital stationary night blindness autosomal dominant 2
congenital stationary night blindness autosomal dominant 2
Explore linked clinical trials. Standard reference: MONDO:00080991 results ยท Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Natural History Study in Patients With PDE6A-, PDE6B- and RHO-linked Retinitis Pigmentosa | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, congenital stationary night blindness autosomal dominant 1, congenital stationary night blindness autosomal dominant 2, eye disorder, hereditary disease, inherited retinal dystrophy, retinal degeneration, retinal disorder, retinitis pigmentosa | Active, not recruiting | Not stated | 2026-05-06 | NCT06323772 |