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| Adult onset dystonia, chorea or related movement disorder v0.88 | NPC2 | Louise Daugherty edited their review of gene: NPC2: 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 | NPC2 | Louise Daugherty reviewed gene: NPC2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Adult onset dystonia, chorea or related movement disorder v0.49 | NPC2 | Emily Jones reviewed gene: NPC2: Rating: RED; Mode of pathogenicity: ; Publications: 11567215; Phenotypes: Niemann-pick disease, type C2, 607625; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Adult onset dystonia, chorea or related movement disorder v0.48 | NPC2 |
Louise Daugherty Added phenotypes Niemann-pick disease, type C2, 607625 for gene: NPC2 Publications for gene NPC2 were changed from to 11567215 |
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| Adult onset dystonia, chorea or related movement disorder v0.47 | NPC2 | Louise Daugherty Source NHS GMS was added to NPC2. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Adult onset dystonia, chorea or related movement disorder v0.46 | NPC2 | Louise Daugherty Source South West GLH was added to NPC2. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Adult onset dystonia, chorea or related movement disorder v0.2 | NPC2 |
Ellen McDonagh gene: NPC2 was added gene: NPC2 was added to Adult onset movement disorder. Sources: Expert Review Red Mode of inheritance for gene: NPC2 was set to Phenotypes for gene: NPC2 were set to Dystonia |
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