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| Structural eye disease v0.76 | MYH9 | Nicola Ragge reviewed gene: MYH9: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Epstein Syndrome, Fechtner syndrome, 153650, 153640 ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.49 | MYH9 | Ivone Leong edited their review of gene: MYH9: Changed phenotypes: Epstein Syndrome, Fechtner syndrome, 153650, 153640 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.39 | MYH9 | Ivone Leong reviewed gene: MYH9: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Neurofibromatosis, Type II, 101000; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.13 | MYH9 |
Ivone Leong gene: MYH9 was added gene: MYH9 was added to Structural eye disease. Sources: NHS GMS Mode of inheritance for gene: MYH9 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: MYH9 were set to Epstein Syndrome, 153650; Fechtner syndrome, 153640 |
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