| Panel | Mode of inheritance | Details |
|---|---|---|
1 panel | ||
Green in Retinal disordersR-numbers: R32 Signed-off version 4.42 | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | Phenotypes Achromatopsia, Cone, and Cone-rod Dystrophy, Cone-rod dystrophy 6 (AD), Leber congenital amaurosis 1 (AR), Leber congenital amaurosis 1, 204000, Eye Disorders, Retinitis pigmentosa |