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| Childhood onset dystonia, chorea or related movement disorder v2.2 | COX10 | Arina Puzriakova Phenotypes for gene: COX10 were changed from Mitochondrial complex IV deficiency, 220110; Leigh syndrome due to mitochondrial COX4 deficiency, 256000 to Mitochondrial complex IV deficiency, nuclear type 3, OMIM:619046 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Childhood onset dystonia, chorea or related movement disorder v0.7 | COX10 |
Ellen McDonagh Source PanelApp was added to COX10. Mode of inheritance for gene COX10 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Mitochondrial complex IV deficiency, 220110; Leigh syndrome due to mitochondrial COX4 deficiency, 256000 for gene: COX10 Publications for gene COX10 were changed from to 10767350 |
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| Childhood onset dystonia, chorea or related movement disorder v0.0 | COX10 |
Ellen McDonagh gene: COX10 was added gene: COX10 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Green Mode of inheritance for gene: COX10 was set to |
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