CNGB3

cyclic nucleotide gated channel beta 3
OMIM: 605080
PanelMode of inheritanceDetails
1 panel
R-numbers: R32, R33, R34, R35
Signed-off version 2.195
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Achromatopsia, Macular degeneration, juvenile, Achromatopsia-3, 262300, Macular degeneration, juvenile, 248200 -3, Stargardt Disease, Recessive, Macular Dystrophy/Degeneration/Stargardt Disease, Achromatopsia-3, Eye Disorders, Achromatopsia, Cone, and Cone-rod Dystrophy