NRL

neural retina leucine zipper
OMIM: 162080
PanelMode of inheritanceDetails
1 panel
R-numbers: R32
Signed-off version 3.3
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Retinal degeneration, autosomal recessive, clumped pigment type (AR), Retinitis pigmentosa 27 (AD), Eye Disorders, Retinitis Pigmentosa, Dominant, Retinitis pigmentosa, Retinitis pigmentosa 27, 613750