Any congenital stationary night blindness in which the cause of the disease is a mutation in the LRIT3 gene.
Comprehensive, easy-to-understand information about this condition
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congenital stationary night blindness autosomal dominant 2
MONDO:0008099
congenital stationary night blindness 1B
MONDO:0009758
cone-rod synaptic disorder, congenital nonprogressive
MONDO:0012490
congenital stationary night blindness autosomal dominant 3
MONDO:0012497
congenital stationary night blindness autosomal dominant 1
MONDO:0012498
congenital stationary night blindness 1C
MONDO:0013183