| Panel | Mode of inheritance | Details |
|---|---|---|
1 panel | ||
Green in Retinal disordersR-numbers: R32 Signed-off version 6.16 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Achromatopsia, Cone, and Cone-rod Dystrophy, Eye Disorders, Cone-Rod Dystrophy, Dominant, CD4 lymphopenia, idiopathic (Gorska (2012) Blood 119, 1399) |