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| Structural eye disease v0.76 | CYP4V2 | Nicola Ragge reviewed gene: CYP4V2: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Bietti crystalline corneoretinal dystrophy, 210370; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | CYP4V2 | Ivone Leong reviewed gene: CYP4V2: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Bietti crystalline corneoretinal dystrophy, 210370; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | CYP4V2 |
Ivone Leong Source NHS GMS was added to CYP4V2. Mode of inheritance for gene CYP4V2 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Bietti crystalline corneoretinal dystrophy, 210370 for gene: CYP4V2 |
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| Structural eye disease v0.2 | CYP4V2 |
Ellen McDonagh gene: CYP4V2 was added gene: CYP4V2 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: CYP4V2 was set to Phenotypes for gene: CYP4V2 were set to Eye Disorders |
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