Panel | Mode of inheritance | Details |
---|---|---|
2 panels | ||
Green in DDG2PComponent of the following Super Panels:
Signed-off version 4.15 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes LEBER CONGENITAL AMAUROSIS 4 604393 |
Green in Retinal disordersR-numbers: R32 Signed-off version 6.16 | BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal | Phenotypes Cone-rod dystrophy, OMIM:604393, Retinitis pigmentosa, juvenile, OMIM:604393, Leber congenital amaurosis 4, OMIM:604393 |