Panel | Mode of inheritance | Details |
---|---|---|
1 panel | ||
Green in Retinal disordersR-numbers: R32 Signed-off version 6.0 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Cone-rod dystrophy 11, OMIM:610381, Retinitis pigmentosa 95, OMIM:620102, ?Macular degeneration, age-related, 6, OMIM:613757 |