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| Syndromic Retinopathy v1.0 | CLN3 | Gene migrated from ENSG00000188603 to ENSG00000188603 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Syndromic Retinopathy v0.0 | CLN3 |
Bryony Thompson gene: CLN3 was added gene: CLN3 was added to Syndromic Retinopathy. Sources: Expert Review Green,RetNet Mode of inheritance for gene: CLN3 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: CLN3 were set to Juvenile neuronal ceroid lipofuscinosis; Retinitis pigmentosa |
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