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| Syndromic Retinopathy v1.0 | PEX7 | Gene migrated from ENSG00000112357 to ENSG00000112357 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Syndromic Retinopathy v0.0 | PEX7 |
Bryony Thompson gene: PEX7 was added gene: PEX7 was added to Syndromic Retinopathy. Sources: Expert Review Green,RetNet Mode of inheritance for gene: PEX7 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: PEX7 were set to Refsum disease |
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