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| Childhood onset dystonia, chorea or related movement disorder v1.205 | SLC30A10 | Arina Puzriakova Phenotypes for gene: SLC30A10 were changed from Dystonia/Parkinsonism, Hypermanganesemia, Polycythemia, and Chronic Liver Disease; Hypermanganesemia with dystonia, polycythemia, and cirrhosis, 613280 to Hypermanganesemia with dystonia 1, OMIM:613280 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Childhood onset dystonia, chorea or related movement disorder v0.7 | SLC30A10 |
Ellen McDonagh Source PanelApp was added to SLC30A10. Mode of inheritance for gene SLC30A10 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Dystonia/Parkinsonism, Hypermanganesemia, Polycythemia, and Chronic Liver Disease; Hypermanganesemia with dystonia, polycythemia, and cirrhosis, 613280 for gene: SLC30A10 Publications for gene SLC30A10 were changed from to 22934317; 22341972; 25778823; 22341971; 22926781 |
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| Childhood onset dystonia, chorea or related movement disorder v0.0 | SLC30A10 |
Ellen McDonagh gene: SLC30A10 was added gene: SLC30A10 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Green Mode of inheritance for gene: SLC30A10 was set to |
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