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| Structural eye disease v0.76 | OPA3 | Nicola Ragge reviewed gene: OPA3: Rating: RED; Mode of pathogenicity: Other - please provide details in the comments; Publications: ; Phenotypes: Optic atrophy 3 with cataract, 165300; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.48 | OPA3 | Ivone Leong edited their review of gene: OPA3: Changed phenotypes: Optic atrophy 3 with cataract, 165300 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | OPA3 | Ivone Leong reviewed gene: OPA3: Rating: RED; Mode of pathogenicity: Other - please provide details in the comments; Publications: ; Phenotypes: Glaucoma 1, open angle, E, 137760; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | OPA3 |
Ivone Leong Source NHS GMS was added to OPA3. Mode of inheritance for gene OPA3 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Added phenotypes Optic atrophy 3 with cataract, 165300 for gene: OPA3 |
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| Structural eye disease v0.2 | OPA3 |
Ellen McDonagh gene: OPA3 was added gene: OPA3 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: OPA3 was set to Phenotypes for gene: OPA3 were set to Eye Disorders |
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