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| Cone-rod Dystrophy v1.0 | PRPH2 | Gene migrated from ENSG00000112619 to ENSG00000112619 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Cone-rod Dystrophy v0.0 | PRPH2 |
Bryony Thompson gene: PRPH2 was added gene: PRPH2 was added to Cone-rod Dystrophies. Sources: Royal Melbourne Hospital,Expert Review Green Mode of inheritance for gene: PRPH2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: PRPH2 were set to 30679166 Phenotypes for gene: PRPH2 were set to Choroidal dystrophy, central areolar 2 MIM#613105 |
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