5 entries on 1 page. Showing entries 1 - 5.

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ID	Abbreviation	Name	OMIM ID	Individuals	Phenotypes	Associated with genes	Associated tissues	Disease features
00170	556500	PARKINSON DISEASE, MITOCHONDRIAL	556500	0	0	MT-TK, NDUFV2	-	-
00163	MELAS SYNDROME	MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES;DOID:3687	540000	1	1	MT-ND1, MT-ND4, MT-ND5, MT-ND6, MT-TC, MT-TF, MT-TH, MT-TK, MT-TL1, MT-TQ, MT-TS1, MT-TS2	-	-
00162	MERRF	MYOCLONIC EPILEPSY ASSOCIATED WITH RAGGED-RED FIBERS; MERRF SYNDROME	545000	1	0	MT-ND5, MT-TF, MT-TH, MT-TK, MT-TL1, MT-TS1, MT-TS2	-	-
00165	MIDD	DIABETES AND DEAFNESS, MATERNALLY INHERITED;MIDD	520000	0	0	MT-TE, MT-TK, MT-TL1	-	-
00026	MTDPS1	Mitochondrial DNA depletion syndrome 1 (MNGIE type), 603041 (3)	603041	0	0	MT-TK, POLG, TYMP	-	-

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