Search results for NADH

112 hits were found for NADH

#	Family	MCID	Name	MIFTS	Score
1		MTC007	Mitochondrial Complex I Deficiency	57	10.236

2		MTH026	Methemoglobinemia Due to Deficiency of Methemoglobin Reductase	33	9.181

3		FTL050	Fatal Infantile Hypertrophic Cardiomyopathy Due to Mitochondrial Complex I Deficiency	7	3.321

4		PYR031	Pyruvate Dehydrogenase E3-Binding Protein Deficiency	38	2.480

5	P	MPL001	Maple Syrup Urine Disease	65	2.348

6		DHY010	Dihydrolipoamide Dehydrogenase Deficiency	34	2.348

7	P	MTH007	Methemoglobinemia	47	0.328

8	c	HRD146	Hereditary Methemoglobinemia	31	0.305

9		MTH064	Methemoglobinemia, Beta-Globin Type	39	0.213

10	c	CNG223	Congenital Methemoglobinemia	30	0.213

11		TYP041	Type I	56	0.199

12		AGN016	Aging	64	0.159

13	P	NRP001	Neuropathy	63	0.130

14		OPT006	Optic Nerve Disease	57	0.130

15	P	BRS047	Breast Cancer	100	0.119

16		END072	Endotheliitis	45	0.119

17	P	ALZ034	Alzheimer Disease	87	0.106

18		LBR002	Leber Hereditary Optic Neuropathy	57	0.106

19		ART140	Arteries, Anomalies of	65	0.092

20		MTH072	Methemoglobin Reductase Deficiency	21	0.092

21		SCC003	Succinic Acidemia	12	0.092

22		DPR016	Depression	72	0.075

23		CHG001	Chagas Disease	71	0.075

24	P	PNM007	Pneumonia	69	0.075

25	P	MYP004	Myopathy	68	0.075

26	P	CRN018	Coronary Artery Anomaly	68	0.075

27		CHR066	Chronic Fatigue Syndrome	66	0.075

28	P	DYS154	Dystonia	64	0.075

29	P	ENC018	Encephalopathy	62	0.075

30		MTC114	Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes	61	0.075

31		CHL014	Cholera	56	0.075

32	P	CRV039	Cervicitis	49	0.075

33	c	SPR009	Sporadic Breast Cancer	46	0.075

34	P	MTC004	Mitochondrial Encephalomyopathy	43	0.075

35		PHC013	Phaeochromocytoma	43	0.075

36		DYS015	Dysentery	43	0.075

37		NRN002	Neuronitis	41	0.075

38	P	ENC011	Encephalomyopathy	40	0.075

39		CRT020	Cortisone Reductase Deficiency	25	0.075

40	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	91	0.053

41		CYS001	Cystic Fibrosis	84	0.053

42		MLR004	Malaria	83	0.053

43	c	LKM061	Leukemia, Acute Myeloid	80	0.053

44		GST053	Gastric Cancer	77	0.053

45	P	DLT002	Dilated Cardiomyopathy	76	0.053

46	P	HPT021	Hepatitis	76	0.053

47	P	NRB001	Neuroblastoma	72	0.053

48		PLM129	Pulmonary Disease, Chronic Obstructive	72	0.053

49	P	LKM002	Leukemia	72	0.053

50	c	HPT073	Hepatitis C Virus	72	0.053

51		PSY004	Psychotic Disorder	71	0.053

52	c	HPT001	Hepatitis C	71	0.053

53		CRB037	Cerebral Palsy	71	0.053

54	P	ATS364	Autism	70	0.053

55	P	LYM118	Lymphoma	70	0.053

56	P	CRV035	Cervical Cancer	69	0.053

57	P	SCH015	Schizophrenia	69	0.053

58		DWN001	Down Syndrome	69	0.053

59	P	MYL006	Myeloid Leukemia	68	0.053

60		BRK010	Burkitt Lymphoma	68	0.053

61		ISC004	Ischemia	65	0.053

62	P	END044	Endometriosis	64	0.053

63	P	HYP061	Hypertrophic Cardiomyopathy	64	0.053

64	P	PNC044	Pancreatitis	64	0.053

65	c	OVR114	Ovarian Cancer 1	62	0.053

66	P	MCH002	Machado-Joseph Disease	62	0.053

67		HYP056	Hypoglycemia	62	0.053

68		HYP266	Hypoxia	61	0.053

69		NRM005	Neuromuscular Disease	60	0.053

70	P	CTR002	Cataract	60	0.053

71		RNL114	Renal Cell Carcinoma, Nonpapillary	59	0.053

72	c	3MT016	3-Methylglutaconic Aciduria, Type Iii	59	0.053

73	P	BPL003	Bipolar Disorder	59	0.053

74		SLP005	Sleep Disorder	59	0.053

75	c	PRC016	Pre-Eclampsia	59	0.053

76		ORL011	Oral Cancer	59	0.053

77	P	ECL001	Eclampsia	57	0.053

78		ECH003	Echinococcosis	56	0.053

79	P	THY032	Thyroiditis	55	0.053

80		SPP010	Suppressor of Tumorigenicity 3	54	0.053

81	P	MTC133	Mitochondrial Myopathy	54	0.053

82	P	GLM045	Glioma	54	0.053

83		PRP080	Peripheral Artery Disease	53	0.053

84	P	MSC033	Muscle Disorders	52	0.053

85		ONC002	Onchocerciasis	52	0.053

86		ALV002	Alveolar Echinococcosis	51	0.053

87		ATN002	Autonomic Nervous System Disease	51	0.053

88	P	LCT001	Lactic Acidosis	50	0.053

89		ATN005	Autonomic Dysfunction	50	0.053

90	P	MYP087	Myopathy, Tubular Aggregate, 1	49	0.053

91		ANX004	Anoxia	49	0.053

92		CLR030	Clear Cell Renal Cell Carcinoma	49	0.053

93	P	BRN006	Branchiootorenal Syndrome	47	0.053

94		SPS007	Spastic Cerebral Palsy	47	0.053

95	c	MTR002	Mitral Valve Insufficiency	46	0.053

96	c	EST002	Estrogen-Receptor Negative Breast Cancer	44	0.053

97	P	DYS021	Dysautonomia	43	0.053

98	c	CHR095	Chronic Progressive External Ophthalmoplegia	43	0.053

99		CRB009	Cerebritis	41	0.053

100		SPS057	Spasticity	41	0.053

101		PRG039	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3	40	0.053

102		SNL007	Senile Cataract	40	0.053

103		MSC004	Muscle Tissue Disease	39	0.053

104	c	MLG068	Malignant Glioma	38	0.053

105		ORG002	Organic Acidemia	38	0.053

106		PRG130	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1	36	0.053

107		PRG040	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4	36	0.053

108		PRG038	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2	36	0.053

109		PNB004	Panbronchiolitis, Diffuse	35	0.053

110	c	PRK085	Parkinson Disease 1, Autosomal Dominant	31	0.053

111		BRN121	Branchiootorenal/branchiootic Syndrome	20	0.053

112		LCT008	Lactate Dehydrogenase Deficiency	16	0.053