NR2E3

nuclear receptor subfamily 2 group E member 3
OMIM: 604485
PanelMode of inheritanceDetails
1 panel
R-numbers: R32
Signed-off version 3.3
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Enhanced S - cone syndrome (AR), Retinitis pigmentosa 37 (AD and AR), Eye Disorders, Retinitis pigmentosa, Retinitis Pigmentosa, Recessive, Enhanced S-cone syndrome, 268100