| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Childhood onset dystonia, chorea or related movement disorder v0.1 | GAMT |
Ellen McDonagh Source South West GLH was added to GAMT. Mode of inheritance for gene GAMT was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Cerebral creatine deficiency syndrome 2, 612736 for gene: GAMT |
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| Childhood onset dystonia, chorea or related movement disorder v0.0 | GAMT |
Ellen McDonagh gene: GAMT was added gene: GAMT was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Red Mode of inheritance for gene: GAMT was set to |
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| Childhood onset dystonia, chorea or related movement disorder v0.0 | CAMTA1 |
Ellen McDonagh gene: CAMTA1 was added gene: CAMTA1 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Red Mode of inheritance for gene: CAMTA1 was set to |
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| Childhood onset dystonia, chorea or related movement disorder v0.0 | AMT |
Ellen McDonagh gene: AMT was added gene: AMT was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Red Mode of inheritance for gene: AMT was set to |
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