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| Childhood onset dystonia, chorea or related movement disorder v0.67 | KCTD17 | Ellen McDonagh Phenotypes for gene: KCTD17 were changed from to Dystonia 26, myoclonic | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Childhood onset dystonia, chorea or related movement disorder v0.66 | KCTD17 | Ellen McDonagh Mode of inheritance for gene: KCTD17 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Childhood onset dystonia, chorea or related movement disorder v0.0 | KCTD17 |
Ellen McDonagh gene: KCTD17 was added gene: KCTD17 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Green Mode of inheritance for gene: KCTD17 was set to |
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