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19 Jun 2019	Structural eye disease v0.76	LRIT3	Nicola Ragge reviewed gene: LRIT3: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Night blindness, congenital stationary (complete), 1F, autosomal recessive, 615058; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
17 Apr 2019	Structural eye disease v0.38	LRIT3	Ivone Leong reviewed gene: LRIT3: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Night blindness, congenital stationary (complete), 1F, autosomal recessive, 615058; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
17 Apr 2019	Structural eye disease v0.15	LRIT3	Ivone Leong Source NHS GMS was added to LRIT3. Mode of inheritance for gene LRIT3 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Night blindness, congenital stationary (complete), 1F, autosomal recessive, 615058 for gene: LRIT3
03 Jan 2019	Structural eye disease v0.2	LRIT3	Ellen McDonagh gene: LRIT3 was added gene: LRIT3 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: LRIT3 was set to Phenotypes for gene: LRIT3 were set to Eye Disorders