| Panel | Mode of inheritance | Details |
|---|---|---|
1 panel | ||
Green in Retinal disordersR-numbers: R32 Signed-off version 7.0 | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | Phenotypes Night blindness, congenital stationary, autosomal dominant 2, Retinitis pigmentosa 40, Congenital Stationary Night Blindness, Dominant, Congenital Stationary Night Blindness, Night blindness, congenital stationary, autosomal dominant 2, 163500, Retinitis pigmentosa, Retinitis Pigmentosa, Recessive |