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Childhood onset dystonia, chorea or related movement disorder v0.7 | PMM2 |
Ellen McDonagh Source PanelApp was added to PMM2. Mode of inheritance for gene PMM2 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Congenital disorder of glycosylation, type Ia 212065 for gene: PMM2 Publications for gene PMM2 were changed from to 9140401 |
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Childhood onset dystonia, chorea or related movement disorder v0.0 | PMM2 |
Ellen McDonagh gene: PMM2 was added gene: PMM2 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Red Mode of inheritance for gene: PMM2 was set to |