| Panel | Mode of inheritance | Details |
|---|---|---|
1 panel | ||
Green in Retinal disordersR-numbers: R32 Signed-off version 7.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Achromatopsia, Cone, and Cone-rod Dystrophy, Cone-rod synaptic disorder, congenital nonprogressive, Congenital Stationary Night Blindness, Night blindness, congenital stationary (incomplete), 2B, autosomal recessive, 610427 |