PanelApp (test)
  1. Genes and Genomic Entities
  2. LRIT3

LRIT3

leucine rich repeat, Ig-like and transmembrane domains 3
OMIM: 615004, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green LRIT3 in Mendeliome


Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Night blindness, congenital stationary (complete), 1F, autosomal recessive, MIM# 615058

Green LRIT3 in Congenital Stationary Night Blindness


Level 2: Ophthalmological disorders
Version 1.0

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Royal Melbourne Hospital
Phenotypes
  • Night blindness, congenital stationary (complete), 1F, autosomal recessive, 615058

Red LRIT3 in Congenital nystagmus


Level 2: Ophthalmological disorders
Version 2.0

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert Review Red
  • Royal Melbourne Hospital
  • Victorian Clinical Genetics Services
Phenotypes
  • Night blindness, congenital stationary (complete), 1F, autosomal recessive, 615058