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Date	Panel	Item	Activity
Filter activities 4 actions
21 Dec 2022	Intellectual disability 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	COX15	BRIDGE consortium edited their review of COX15
27 Jul 2017	Intellectual disability	COX15	BRIDGE consortium edited their review of COX15
19 Jul 2017	Intellectual disability	COX15	BRIDGE consortium reviewed COX15