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| Childhood onset dystonia, chorea or related movement disorder v0.256 | FOXRED1 | Louise Daugherty commented on gene: FOXRED1: Confirmed Green rating - as per recommendation from Specialist Test Group (via Robyn Labrum LNGLH) 12 December 2019. Also on mitochondrial panel, more of a mitochondrial phenotype but may present early with movement disorder. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Childhood onset dystonia, chorea or related movement disorder v0.110 | FOXRED1 | Louise Daugherty Added comment: Comment on mode of inheritance: changed from unknown to biallelic | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Childhood onset dystonia, chorea or related movement disorder v0.110 | FOXRED1 | Louise Daugherty Mode of inheritance for gene: FOXRED1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Childhood onset dystonia, chorea or related movement disorder v0.1 | FOXRED1 |
Ellen McDonagh Source South West GLH was added to FOXRED1. Mode of inheritance for gene FOXRED1 was changed from to Unknown Added phenotypes Mitochondrial complex I deficiency, nuclear type 19, 618241 for gene: FOXRED1 |
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| Childhood onset dystonia, chorea or related movement disorder v0.0 | FOXRED1 |
Ellen McDonagh gene: FOXRED1 was added gene: FOXRED1 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Green Mode of inheritance for gene: FOXRED1 was set to |
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