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ID	Abbreviation	Name	OMIM ID	Individuals	Phenotypes	Associated with genes	Associated tissues	Disease features
00010	615228	Mitochondrial complex (ATP synthase) deficiency, nuclear type 4, 615228 (3)	615228	0	0	ATP5A1, ATP5F1A	-	-
00502	616045	?Combined oxidative phosphorylation deficiency 22, 616045 (3)	616045	0	0	ATP5A1, ATP5F1A	-	-

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