| Panel | Mode of inheritance | Details |
|---|---|---|
1 panel | ||
Green in Retinal disordersR-numbers: R32 Signed-off version 7.0 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Cone dystrophy-3, 602093, Eye Disorders, Achromatopsia, Cone, and Cone-rod Dystrophy |