Genomics England
GMS Panels
Panels
Genes and Entities

LRIT3

leucine rich repeat, Ig-like and transmembrane domains 3
OMIM: 615004
PanelMode of inheritanceDetails
2 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.15
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
AUTOSOMAL-RECESSIVE COMPLETE CONGENITAL STATIONARY NIGHT BLINDNESS 615058
Green
in Retinal disorders
R-numbers: R32
Signed-off version 6.16
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Congenital Stationary Night Blindness, Congenital Stationary Night Blindness, Recessive, Night blindness, congenital stationary (complete), 1F, autosomal recessive, 615058