4 entries on 1 page. Showing entries 1 - 4.

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ID	Abbreviation	Name	OMIM ID	Individuals	Phenotypes	Associated with genes	Associated tissues	Disease features
00151	500000	CARDIOMYOPATHY, INFANTILE HISTIOCYTOID	500000	0	0	MT-CYB	-	-
00114	601665	Obesity, autosomal dominant, 601665 (3)	601665	0	0	, ADRB2, ADRB3, AGRP, CARTPT, ENPP1, GHRL, KANK1, LEPR, MC4R, more than 10, MRAP2, MT-CYB, NR0B2, POMC, PPARG, PPARGC1B, PYY, SDC3, SIM1, UCP1, UCP3	-	-
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	-	-
00465	MTCYB	CYTOCHROME b OF COMPLEX III; MTCYB	516020	0	0	, MT-CYB	-	-

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