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| Childhood onset dystonia, chorea or related movement disorder v0.7 | CC2D2A |
Ellen McDonagh Source PanelApp was added to CC2D2A. Mode of inheritance for gene CC2D2A was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Joubert syndrome with oculorenal defect; Meckel syndrome 6; Meckel syndrome; COACH syndrome; Joubert syndrome 9 for gene: CC2D2A |
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| Childhood onset dystonia, chorea or related movement disorder v0.0 | CC2D2A |
Ellen McDonagh gene: CC2D2A was added gene: CC2D2A was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Red Mode of inheritance for gene: CC2D2A was set to |
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