Panel | Mode of inheritance | Details |
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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 |