| Panel | Mode of inheritance | Details |
|---|---|---|
1 panel | ||
Green in Retinal disordersR-numbers: R32 Signed-off version 4.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Achromatopsia, Achromatopsia-2, 216900, Eye Disorders, Achromatopsia, Cone, and Cone-rod Dystrophy |