CNGB3

cyclic nucleotide gated channel beta 3
OMIM: 605080
PanelMode of inheritanceDetails
2 panels
R-numbers: R39
Signed-off version 4.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Achromatopsia 3, OMIM:262300
R-numbers: R32
Signed-off version 8.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Achromatopsia 3, OMIM:262300, Macular degeneration, juvenile