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| Childhood onset dystonia, chorea or related movement disorder v0.252 | SYNJ1 | Louise Daugherty Phenotypes for gene: SYNJ1 were changed from Parkinson disease 20, early-onset; juvenile Parkinsonism to Parkinson disease 20, early-onset, 615530; juvenile Parkinsonism | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Childhood onset dystonia, chorea or related movement disorder v0.7 | SYNJ1 |
Ellen McDonagh Source PanelApp was added to SYNJ1. Mode of inheritance for gene SYNJ1 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Parkinson disease 20, early-onset; juvenile Parkinsonism for gene: SYNJ1 Publications for gene SYNJ1 were changed from to 27496670; 23804577; 23804563 |
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| Childhood onset dystonia, chorea or related movement disorder v0.0 | SYNJ1 |
Ellen McDonagh gene: SYNJ1 was added gene: SYNJ1 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Green Mode of inheritance for gene: SYNJ1 was set to |
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