PDE6B

phosphodiesterase 6B
OMIM: 180072
PanelMode of inheritanceDetails
1 panel
R-numbers: R32
Signed-off version 5.4
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Night blindness, congenital stationary, autosomal dominant 2, Retinitis pigmentosa 40, Congenital Stationary Night Blindness, Dominant, Congenital Stationary Night Blindness, Night blindness, congenital stationary, autosomal dominant 2, 163500, Retinitis pigmentosa, Retinitis Pigmentosa, Recessive