| Panel | Mode of inheritance | Details |
|---|---|---|
1 panel | ||
Green in Retinal disordersR-numbers: R32 Signed-off version 4.42 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Lebers congenital amaurosis, retinal dystrophy, ?Leber congenital amaurosis 19, OMIMM:618513 |