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ID	Abbreviation	Name	OMIM ID	Individuals	Phenotypes	Associated with genes	Associated tissues	Disease features
00012	220110	Mitochondrial complex IV deficiency, 220110 (3)	220110	1	0	APOPT1, COA5, COA7, COX10, COX14, COX20, COX6B1, COX8A, FASTKD2, MT-CO1, MT-CO2, MT-CO3, MT-TL1, MT-TN, PET100, SCO1, SURF1, TACO1	-	-
00166	550500	MYOGLOBINURIA, RECURRENT	550500	0	0	MT-CO1	-	-
00051	580000	DEAFNESS, AMINOGLYCOSIDE-INDUCED;STREPTOMYCIN-INDUCED	580000	0	0	, MT-CO1, MT-RNR1, TRMU	-	-

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