| Panel | Mode of inheritance | Details |
|---|---|---|
1 panel | ||
Green in Retinal disordersR-numbers: R32 Signed-off version 4.0 | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | Phenotypes Night blindness, congenital stationary autosomal dominant 1, Retinitis pigmentosa, Retinitis punctata albescens, Congenital Stationary Night Blindness, Retinitis pigmentosa 4, autosomal dominant or recessive, 613731, Retinitis Pigmentosa, Dominant/Recessive, Retinitis pigmentosa |