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Structural eye disease v0.76 | ELOVL4 | Nicola Ragge reviewed gene: ELOVL4: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Stargardt disease 3, 600110; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Structural eye disease v0.38 | ELOVL4 | Ivone Leong reviewed gene: ELOVL4: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Stargardt disease 3, 600110; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Structural eye disease v0.15 | ELOVL4 |
Ivone Leong Source NHS GMS was added to ELOVL4. Mode of inheritance for gene ELOVL4 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Added phenotypes Stargardt disease 3, 600110 for gene: ELOVL4 |
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Structural eye disease v0.2 | ELOVL4 |
Ellen McDonagh gene: ELOVL4 was added gene: ELOVL4 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: ELOVL4 was set to Phenotypes for gene: ELOVL4 were set to Eye Disorders |