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Date	Panel	Item	Activity
Filter activities 5 actions
25 Oct 2024	Dystonia, chorea or related movement disorder, childhood onset v5.7	VPS13D	Arina Puzriakova Phenotypes for gene: VPS13D were changed from Spinocerebellar ataxia, autosomal recessive 4, 607317 to Spinocerebellar ataxia, autosomal recessive 4, OMIM:607317
08 Dec 2019	Dystonia, chorea or related movement disorder, childhood onset v0.213	VPS13D	Louise Daugherty Phenotypes for gene: VPS13D were changed from Spinocerebellar ataxia, autosomal recessive 4 to Spinocerebellar ataxia, autosomal recessive 4, 607317
06 Dec 2019	Dystonia, chorea or related movement disorder, childhood onset v0.102	VPS13D	Ellen McDonagh Phenotypes for gene: VPS13D were changed from to Spinocerebellar ataxia, autosomal recessive 4
06 Dec 2019	Dystonia, chorea or related movement disorder, childhood onset v0.101	VPS13D	Ellen McDonagh Mode of inheritance for gene: VPS13D was changed from to BIALLELIC, autosomal or pseudoautosomal
06 Dec 2019	Dystonia, chorea or related movement disorder, childhood onset v0.0	VPS13D	Ellen McDonagh gene: VPS13D was added gene: VPS13D was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Green Mode of inheritance for gene: VPS13D was set to