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Adult onset dystonia, chorea or related movement disorder v0.88 DRD5 Louise Daugherty edited their review of gene: DRD5: Added comment: This panel was initially created as a merge of genomic entities from the following Rare Disease 100K panels - Early onset dystonia (v1.76, code 192) - Parkinson Disease and Complex Parkinsonism (v1.64, code 39) - Brain channelopathy (v1.48, code 90) - Structural basal ganglia disorders (v1.10, code 180). This gene was RED and external expert review from South West GLH for GMS Neurology specialist test group for R56 agrees this gene should remain RED; Changed rating: RED
Adult onset dystonia, chorea or related movement disorder v0.50 DRD5 Louise Daugherty reviewed gene: DRD5: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Adult onset dystonia, chorea or related movement disorder v0.49 DRD5 Emily Jones reviewed gene: DRD5: Rating: RED; Mode of pathogenicity: ; Publications: 17133500, 12700316; Phenotypes: {Blepharospasm, primary benign}, 606798; Mode of inheritance:
Adult onset dystonia, chorea or related movement disorder v0.48 DRD5 Louise Daugherty Added phenotypes {Blepharospasm, primary benign}, 606798 for gene: DRD5
Publications for gene DRD5 were changed from PMID: 17133500 to 12700316; 17133500
Adult onset dystonia, chorea or related movement disorder v0.47 DRD5 Louise Daugherty Source NHS GMS was added to DRD5.
Adult onset dystonia, chorea or related movement disorder v0.46 DRD5 Louise Daugherty Source South West GLH was added to DRD5.
Adult onset dystonia, chorea or related movement disorder v0.2 DRD5 Ellen McDonagh gene: DRD5 was added
gene: DRD5 was added to Adult onset movement disorder. Sources: Expert Review Red
Mode of inheritance for gene: DRD5 was set to
Publications for gene: DRD5 were set to PMID: 17133500
Phenotypes for gene: DRD5 were set to {Blepharospasm, primary benign}, 606798