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Childhood onset dystonia, chorea or related movement disorder v3.3 SPG7 Sarah Leigh commented on gene: SPG7
Childhood onset dystonia, chorea or related movement disorder v3.3 SPG7 Sarah Leigh Mode of inheritance for gene: SPG7 was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Childhood onset dystonia, chorea or related movement disorder v3.2 SPG7 Sarah Leigh Phenotypes for gene: SPG7 were changed from Spastic paraplegia 7, 607259 to Spastic paraplegia 7, autosomal recessive, OMIM:607259; hereditary spastic paraplegia 7, MONDO:0011803
Childhood onset dystonia, chorea or related movement disorder v0.183 SPG7 Louise Daugherty Mode of inheritance for gene: SPG7 was changed from to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Childhood onset dystonia, chorea or related movement disorder v0.182 SPG7 Louise Daugherty Phenotypes for gene: SPG7 were changed from to Spastic paraplegia 7, 607259
Childhood onset dystonia, chorea or related movement disorder v0.0 SPG7 Ellen McDonagh gene: SPG7 was added
gene: SPG7 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: Expert Review Amber,London North GLH
Mode of inheritance for gene: SPG7 was set to