Congenital Stationary Night Blindness
Gene: LRIT3
Three families and two supportive animal models.Created: 25 Oct 2021, 6:55 a.m. | Last Modified: 25 Oct 2021, 6:55 a.m.
Panel Version: 0.14
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Night blindness, congenital stationary (complete), 1F, autosomal recessive, MIM# 615058
Publications
total of 3 individuals reported thus farCreated: 25 Oct 2021, 12:36 a.m. | Last Modified: 25 Oct 2021, 12:36 a.m.
Panel Version: 0.11
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Night blindness, congenital stationary (complete), 1F MIM#615058
Publications
Variants in this GENE are reported as part of current diagnostic practice
Gene: lrit3 has been classified as Green List (High Evidence).
Publications for gene: LRIT3 were set to
gene: LRIT3 was added gene: LRIT3 was added to Congenital Stationary Night Blindness_RMH. Sources: Royal Melbourne Hospital,Expert Review Green Mode of inheritance for gene: LRIT3 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: LRIT3 were set to Night blindness, congenital stationary (complete), 1F, autosomal recessive, 615058