LRIT3

leucine rich repeat, Ig-like and transmembrane domains 3
OMIM: 615004
PanelMode of inheritanceDetails
1 panel
R-numbers: R32
Signed-off version 3.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Congenital Stationary Night Blindness, Congenital Stationary Night Blindness, Recessive, Night blindness, congenital stationary (complete), 1F, autosomal recessive, 615058