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Dystonia, chorea or related movement disorder, childhood onset v1.133 ACOX1 Ivone Leong Phenotypes for gene: ACOX1 were changed from Peroxisomal acyl-CoA oxidase deficiency, 264470 to Peroxisomal acyl-CoA oxidase deficiency, OMIM:264470
Dystonia, chorea or related movement disorder, childhood onset v0.109 ACOX1 Louise Daugherty Added comment: Comment on phenotypes: Added phenotype from OMIM
Dystonia, chorea or related movement disorder, childhood onset v0.109 ACOX1 Louise Daugherty Phenotypes for gene: ACOX1 were changed from to Peroxisomal acyl-CoA oxidase deficiency, 264470
Dystonia, chorea or related movement disorder, childhood onset v0.27 ACOX1 Ellen McDonagh Added comment: Comment on mode of inheritance: Confirmed in OMIM
Dystonia, chorea or related movement disorder, childhood onset v0.27 ACOX1 Ellen McDonagh Mode of inheritance for gene: ACOX1 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal
Dystonia, chorea or related movement disorder, childhood onset v0.26 ACOX1 Ellen McDonagh Mode of inheritance for gene: ACOX1 was changed from to BIALLELIC, autosomal or pseudoautosomal
Dystonia, chorea or related movement disorder, childhood onset v0.0 ACOX1 Ellen McDonagh gene: ACOX1 was added
gene: ACOX1 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Green
Mode of inheritance for gene: ACOX1 was set to