| Panel | Mode of inheritance | Details |
|---|---|---|
1 panel | ||
Green in Retinal disordersR-numbers: R32 Signed-off version 7.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Retinitis pigmentosa 38, childhood onset rod-cone dystrophy with early macular atrophy, Leber congenital amaurosis, Retinitis pigmentosa 38, Eye Disorders, Retinitis pigmentosa, Retinitis Pigmentosa, Recessive, Retinitis pigmentosa 38, 613862 |