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| Childhood onset dystonia, chorea or related movement disorder v0.7 | ATP13A2 |
Ellen McDonagh Source PanelApp was added to ATP13A2. Mode of inheritance for gene ATP13A2 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Kufor-Rakeb syndrome 606693; Parkinson disease; Dystonia for gene: ATP13A2 Publications for gene ATP13A2 were changed from to 21060012 |
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| Childhood onset dystonia, chorea or related movement disorder v0.0 | ATP13A2 |
Ellen McDonagh gene: ATP13A2 was added gene: ATP13A2 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Green Mode of inheritance for gene: ATP13A2 was set to |
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