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| Structural eye disease v0.76 | FAM161A | Nicola Ragge reviewed gene: FAM161A: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinitis pigmentosa 28, 606068; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | FAM161A | Ivone Leong reviewed gene: FAM161A: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinitis pigmentosa 28, 606068; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | FAM161A |
Ivone Leong Source NHS GMS was added to FAM161A. Mode of inheritance for gene FAM161A was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Retinitis pigmentosa 28, 606068 for gene: FAM161A |
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| Structural eye disease v0.2 | FAM161A |
Ellen McDonagh gene: FAM161A was added gene: FAM161A was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: FAM161A was set to Phenotypes for gene: FAM161A were set to Eye Disorders |
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