Search results for mt-co1

#	Family	MCID	Name	MIFTS	Score
26	P	HYP061	Hypertrophic Cardiomyopathy	69	8.128

27		KRT058	Keratoderma, Palmoplantar, with Deafness	44	7.529

28		LBR036	Leber Plus Disease	70	7.529

29		ISL083	Isolated Cytochrome C Oxidase Deficiency	28	7.529

30		GNT042	Genetic Recurrent Myoglobinuria	24	7.529

31	P	OPT006	Optic Nerve Disease	56	7.238

32		CYS008	Cystic Echinococcosis	53	6.846

33		ALV002	Alveolar Echinococcosis	54	6.810

34	P	LCT001	Lactic Acidosis	51	6.026

35		MTC004	Mitochondrial Encephalomyopathy	42	6.026

36		ANG002	Angiostrongyliasis	43	5.945

37	c	CHR095	Chronic Progressive External Ophthalmoplegia	49	5.945

38		MYS004	Myiasis	40	5.945

39	c	HLP023	Holoprosencephaly 1	56	5.747

40	c	NML004	Nemaline Myopathy 3	47	5.747

41		OSB001	Osebold-Remondini Syndrome	35	5.747

42		MTC146	Mitochondrial Complex I Deficiency, Nuclear Type 1	61	5.747

43		MYC072	Myoclonic Epilepsy Associated with Ragged-Red Fibers	48	5.747

44		DFN350	Deafness, Aminoglycoside-Induced	33	5.747

45	c	MYP107	Myopathy, Lactic Acidosis, and Sideroblastic Anemia 3	23	5.747

46	c	PSR032	Psoriasis 11	57	5.747

47		END014	Endemic Typhus	32	5.747

48		STT041	Stuttering	53	5.747

49	c	ATM006	Autoimmune Lymphoproliferative Syndrome	72	5.747

50	c	EPL115	Epilepsy, Familial Temporal Lobe, 2	40	5.747