3 entries on 1 page. Showing entries 1 - 3.

10 per page 25 per page 50 per page 100 per page 250 per page 500 per page 1000 per page

ID	Abbreviation	Name	OMIM ID	Individuals	Phenotypes	Associated with genes	Associated tissues	Disease features
00072	LHON	LEBER OPTIC ATROPHY, LEBER HEREDITARY OPTIC NEUROPATHY; DOID:705	535000	0	0	, MT-ATP6, MT-CO3, MT-CYB, MT-ND1, MT-ND2, MT-ND4, MT-ND4L, MT-ND5, MT-ND6	-	-
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	-	-

10 per page 25 per page 50 per page 100 per page 250 per page 500 per page 1000 per page