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| Childhood onset dystonia, chorea or related movement disorder v0.7 | TMEM237 |
Ellen McDonagh Source PanelApp was added to TMEM237. Mode of inheritance for gene TMEM237 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Joubert syndrome 14; Joubert syndrome; Joubert syndrome with oculorenal defect for gene: TMEM237 Publications for gene TMEM237 were changed from to 20301500; 22152675 |
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| Childhood onset dystonia, chorea or related movement disorder v0.0 | TMEM237 |
Ellen McDonagh gene: TMEM237 was added gene: TMEM237 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Red Mode of inheritance for gene: TMEM237 was set to |
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