CNGA3

cyclic nucleotide gated channel alpha 3
OMIM: 600053
PanelMode of inheritanceDetails
1 panel
R-numbers: R32
Signed-off version 3.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Achromatopsia, Achromatopsia-2, 216900, Eye Disorders, Achromatopsia, Cone, and Cone-rod Dystrophy