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Date	Panel	Item	Activity
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19 Jun 2019	Structural eye disease v0.76	P3H2	Nicola Ragge reviewed gene: P3H2: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: MYOPIA, HIGH, WITH CATARACT AND VITREORETINAL DEGENERATION, 614292; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
18 Apr 2019	Structural eye disease v0.49	P3H2	Ivone Leong edited their review of gene: P3H2: Changed phenotypes: MYOPIA, HIGH, WITH CATARACT AND VITREORETINAL DEGENERATION, 614292
17 Apr 2019	Structural eye disease v0.39	P3H2	Ivone Leong reviewed gene: P3H2: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Waardenburg syndrome, type 3, 148820, Waardenburg syndrome, type 1, 193500; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
17 Apr 2019	Structural eye disease v0.13	P3H2	Ivone Leong gene: P3H2 was added gene: P3H2 was added to Structural eye disease. Sources: NHS GMS Mode of inheritance for gene: P3H2 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: P3H2 were set to MYOPIA, HIGH, WITH CATARACT AND VITREORETINAL DEGENERATION, 614292