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| Adult onset dystonia, chorea or related movement disorder v0.82 | EIF4G1 | Louise Daugherty Classified gene: EIF4G1 as Amber List (moderate evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Adult onset dystonia, chorea or related movement disorder v0.82 | EIF4G1 | Louise Daugherty Gene: eif4g1 has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Adult onset dystonia, chorea or related movement disorder v0.50 | EIF4G1 | Louise Daugherty reviewed gene: EIF4G1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Adult onset dystonia, chorea or related movement disorder v0.49 | EIF4G1 | Emily Jones reviewed gene: EIF4G1: Rating: AMBER; Mode of pathogenicity: ; Publications: 25368108; Phenotypes: Parkinsons disease 18, 614251; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Adult onset dystonia, chorea or related movement disorder v0.48 | EIF4G1 |
Louise Daugherty Added phenotypes Parkinsons disease 18, 614251 for gene: EIF4G1 Publications for gene EIF4G1 were changed from to 25368108 |
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| Adult onset dystonia, chorea or related movement disorder v0.47 | EIF4G1 | Louise Daugherty Source NHS GMS was added to EIF4G1. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Adult onset dystonia, chorea or related movement disorder v0.46 | EIF4G1 | Louise Daugherty Source South West GLH was added to EIF4G1. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Adult onset dystonia, chorea or related movement disorder v0.2 | EIF4G1 |
Ellen McDonagh gene: EIF4G1 was added gene: EIF4G1 was added to Adult onset movement disorder. Sources: Expert Review Red Mode of inheritance for gene: EIF4G1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Phenotypes for gene: EIF4G1 were set to Parkinsons disease 18, 614251 |
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