Panel | Mode of inheritance | Details |
---|---|---|
1 panel | ||
Green in Retinal disordersR-numbers: R32 Signed-off version 6.0 | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | Phenotypes Leber congenital amaurosis 13, Macular Dystrophy/Degeneration/Stargardt Disease, Leber congenital amaurosis 13, 612712, Eye Disorders, Retinitis Pigmentosa, Recessive, Retinitis pigmentosa |