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Date	Panel	Item	Activity
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21 Dec 2022	Intellectual disability - microarray and sequencing v4.23	COX15	Arina Puzriakova Phenotypes for gene: COX15 were changed from Leigh syndrome due to cytochrome c oxidase deficiency, 256000Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2, 615119; MITOCHONDRIAL COMPLEX IV DEFICIENCY (MT-C4D) to Mitochondrial complex IV deficiency, nuclear type 6, OMIM:615119
02 Aug 2017	Intellectual disability - microarray and sequencing	COX15	BRIDGE consortium edited their review of COX15
27 Jul 2017	Intellectual disability - microarray and sequencing	COX15	BRIDGE consortium edited their review of COX15
19 Jul 2017	Intellectual disability - microarray and sequencing	COX15	BRIDGE consortium reviewed COX15