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09 Dec 2019	Childhood onset dystonia, chorea or related movement disorder v0.224	GJC2	Louise Daugherty Phenotypes for gene: GJC2 were changed from Spastic paraplegia 44, autosomal recessive; Leukodystrophy, hypomyelinating, 2 to Spastic paraplegia 44, autosomal recessive, 613206; Leukodystrophy, hypomyelinating, 2, 608804
06 Dec 2019	Childhood onset dystonia, chorea or related movement disorder v0.54	GJC2	Ellen McDonagh Phenotypes for gene: GJC2 were changed from Spastic paraplegia 44, autosomal recessive to Spastic paraplegia 44, autosomal recessive; Leukodystrophy, hypomyelinating, 2
06 Dec 2019	Childhood onset dystonia, chorea or related movement disorder v0.53	GJC2	Ellen McDonagh Phenotypes for gene: GJC2 were changed from to Spastic paraplegia 44, autosomal recessive
06 Dec 2019	Childhood onset dystonia, chorea or related movement disorder v0.52	GJC2	Ellen McDonagh Mode of inheritance for gene: GJC2 was changed from to BIALLELIC, autosomal or pseudoautosomal
06 Dec 2019	Childhood onset dystonia, chorea or related movement disorder v0.0	GJC2	Ellen McDonagh gene: GJC2 was added gene: GJC2 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Green Mode of inheritance for gene: GJC2 was set to