Activity
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| Childhood onset dystonia, chorea or related movement disorder v0.209 | FBXO7 | Louise Daugherty Phenotypes for gene: FBXO7 were changed from juvenile parkinsonism; Dystonia to Parkinson disease 15, autosomal recessive, 260300; juvenile parkinsonism; Dystonia | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Childhood onset dystonia, chorea or related movement disorder v0.7 | FBXO7 |
Ellen McDonagh Source PanelApp was added to FBXO7. Mode of inheritance for gene FBXO7 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes juvenile parkinsonism; Dystonia for gene: FBXO7 |
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| Childhood onset dystonia, chorea or related movement disorder v0.0 | FBXO7 |
Ellen McDonagh gene: FBXO7 was added gene: FBXO7 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Green Mode of inheritance for gene: FBXO7 was set to |
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