RHO

PanelMode of inheritanceDetails
1 panel
R-numbers: R32
Signed-off version 3.3
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Night blindness, congenital stationary autosomal dominant 1, Retinitis pigmentosa, Retinitis punctata albescens, Congenital Stationary Night Blindness, Retinitis pigmentosa 4, autosomal dominant or recessive, 613731, Retinitis Pigmentosa, Dominant/Recessive, Retinitis pigmentosa