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Adult onset dystonia, chorea or related movement disorder v1.44 FBXO7 Arina Puzriakova Phenotypes for gene: FBXO7 were changed from Parkinson disease 15, autosomal recessive, 260300; Parkinson Disease, Recessive; Early Onset Complex Disease; juvenile parkinsonism; Dystonia; parkinsonian-pyramidal syndrome to Parkinson disease 15, autosomal recessive, OMIM:260300
Adult onset dystonia, chorea or related movement disorder v0.54 FBXO7 Louise Daugherty reviewed gene: FBXO7: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Adult onset dystonia, chorea or related movement disorder v0.53 FBXO7 James Polke reviewed gene: FBXO7: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Adult onset dystonia, chorea or related movement disorder v0.52 FBXO7 Louise Daugherty Source NHS GMS was added to FBXO7.
Adult onset dystonia, chorea or related movement disorder v0.51 FBXO7 Louise Daugherty Source London North GLH was added to FBXO7.
Adult onset dystonia, chorea or related movement disorder v0.2 FBXO7 Ellen McDonagh gene: FBXO7 was added
gene: FBXO7 was added to Adult onset movement disorder. Sources: Expert Review Green
Mode of inheritance for gene: FBXO7 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: FBXO7 were set to Parkinson disease 15, autosomal recessive, 260300; Parkinson Disease, Recessive; Early Onset Complex Disease; juvenile parkinsonism; Dystonia; parkinsonian-pyramidal syndrome