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Adult onset dystonia, chorea or related movement disorder v0.88 DCAF10 Louise Daugherty edited their review of gene: DCAF10: 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 DCAF10 Louise Daugherty reviewed gene: DCAF10: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Adult onset dystonia, chorea or related movement disorder v0.49 DCAF10 Emily Jones reviewed gene: DCAF10: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Adult onset dystonia, chorea or related movement disorder v0.47 DCAF10 Louise Daugherty Source NHS GMS was added to DCAF10.
Adult onset dystonia, chorea or related movement disorder v0.46 DCAF10 Louise Daugherty Source South West GLH was added to DCAF10.
Adult onset dystonia, chorea or related movement disorder v0.2 DCAF10 Ellen McDonagh gene: DCAF10 was added
gene: DCAF10 was added to Adult onset movement disorder. Sources: Expert Review Red
Mode of inheritance for gene: DCAF10 was set to BIALLELIC, autosomal or pseudoautosomal