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Childhood onset dystonia, chorea or related movement disorder v0.258 | CHMP2B | Louise Daugherty commented on gene: CHMP2B | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Childhood onset dystonia, chorea or related movement disorder v0.7 | CHMP2B |
Ellen McDonagh Source PanelApp was added to CHMP2B. Mode of inheritance for gene CHMP2B was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Added phenotypes Frontotemporal dementia and/or amyotrophic lateral sclerosis 1; Dystonia; familial frontotemporal lobar degeneration (ALS17) for gene: CHMP2B |
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Childhood onset dystonia, chorea or related movement disorder v0.0 | CHMP2B |
Ellen McDonagh gene: CHMP2B was added gene: CHMP2B was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Red Mode of inheritance for gene: CHMP2B was set to |