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| Childhood onset dystonia, chorea or related movement disorder v2.3 | COX15 | Arina Puzriakova Phenotypes for gene: COX15 were changed from Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2, 615119 to Mitochondrial complex IV deficiency, nuclear type 6, OMIM:615119 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Childhood onset dystonia, chorea or related movement disorder v0.7 | COX15 |
Ellen McDonagh Source PanelApp was added to COX15. Mode of inheritance for gene COX15 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2, 615119 for gene: COX15 |
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| Childhood onset dystonia, chorea or related movement disorder v0.0 | COX15 |
Ellen McDonagh gene: COX15 was added gene: COX15 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Green Mode of inheritance for gene: COX15 was set to |
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