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| Childhood onset dystonia, chorea or related movement disorder v0.7 | TMEM216 |
Ellen McDonagh Source PanelApp was added to TMEM216. Mode of inheritance for gene TMEM216 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Joubert syndrome: Meckel-Gruber syndrome; Joubert syndrome 2; Joubert syndrome with oculorenal defect; Meckel syndrome for gene: TMEM216 Publications for gene TMEM216 were changed from to 22282472; 20512146; 20036350 |
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| Childhood onset dystonia, chorea or related movement disorder v0.0 | TMEM216 |
Ellen McDonagh gene: TMEM216 was added gene: TMEM216 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Red Mode of inheritance for gene: TMEM216 was set to |
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