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ID	Abbreviation	Name	OMIM ID	Individuals	Phenotypes	Associated with genes	Associated tissues	Disease features
00159	500008	DEAFNESS, NONSYNDROMIC SENSORINEURAL, MITOCHONDRIAL	500008	0	0	, MT-ND1, MT-RNR1, MT-TH, MT-TI, MT-TS1	-	-
00051	580000	DEAFNESS, AMINOGLYCOSIDE-INDUCED;STREPTOMYCIN-INDUCED	580000	0	0	, MT-CO1, MT-RNR1, TRMU	-	-

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