Genomics England
GMS Panels
Panels
Genes and Entities
CNGB3
cyclic nucleotide gated channel beta 3
OMIM:
605080
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Panel
Mode of inheritance
Details
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in
Retinal disorders
R-numbers:
R32
Signed-off version 6.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Achromatopsia 3, OMIM:262300, Macular degeneration, juvenile