| 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 Macular Dystrophy/Degeneration/Stargardt Disease, Eye Disorders, Retinitis Pigmentosa, Dominant, Retinitis pigmentosa, Retinitis pigmentosa 48, 613827 |