| Panel | Mode of inheritance | Details |
|---|---|---|
1 panel | ||
Green in Retinal disordersR-numbers: R32 Signed-off version 7.0 | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | Phenotypes Retinitis pigmentosa 1, Eye Disorders, Retinitis pigmentosa 1, 180100{Hypertriglyceridemia, susceptibility to}, 145750, Retinitis Pigmentosa, Dominant, Retinitis pigmentosa, rod-cone dystrophy |