Search results for NADH

290 hits were found for NADH

#	Family	MCID	Name	MIFTS	Score
1		MTC146	Mitochondrial Complex I Deficiency, Nuclear Type 1	60	11.115

2		MTH026	Methemoglobinemia Due to Deficiency of Methemoglobin Reductase	36	9.585

3	P	MPL001	Maple Syrup Urine Disease	69	2.413

4		PYR031	Pyruvate Dehydrogenase E3-Binding Protein Deficiency	42	2.413

5		DHY010	Dihydrolipoamide Dehydrogenase Deficiency	40	2.413

6	P	MTH007	Methemoglobinemia	46	0.346

7	c	CNG223	Congenital Methemoglobinemia	36	0.296

8	P	MTC069	Mitochondrial Disorders	56	0.202

9		ANX004	Anoxia	40	0.191

10	P	MYP004	Myopathy	70	0.174

11	P	LCT001	Lactic Acidosis	51	0.170

12		MTC005	Mitochondrial Metabolism Disease	49	0.165

13	P	MTC133	Mitochondrial Myopathy	49	0.160

14		CYN002	Cyanosis, Transient Neonatal	45	0.151

15		LGH007	Leigh Syndrome	70	0.140

16	P	OPT006	Optic Nerve Disease	60	0.140

17	P	HRD217	Hereditary Optic Neuropathy	36	0.140

18		HYP266	Hypoxia	57	0.129

19		LBR030	Leber Optic Atrophy	60	0.123

20	P	NRB001	Neuroblastoma	72	0.117

21	P	ENC018	Encephalopathy	61	0.117

22	P	NRP001	Neuropathy	56	0.110

23		HLX001	Helix Syndrome	47	0.110

24		CHG001	Chagas Disease	66	0.103

25		CHL014	Cholera	59	0.103

26		HYP056	Hypoglycemia	66	0.095

27	P	VSC007	Vascular Disease	63	0.095

28		CHR066	Chronic Fatigue Syndrome	61	0.095

29		ISC004	Ischemia	58	0.095

30	P	BRS047	Breast Cancer	97	0.087

31		CYS001	Cystic Fibrosis	81	0.087

32	c	ATR087	Atrial Standstill 1	75	0.087

33		PRT037	Pertussis	65	0.087

34		LPD008	Lipid Metabolism Disorder	62	0.087

35		HYP066	Hyperglycemia	61	0.087

36		MTC114	Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes	61	0.087

37	P	MTC004	Mitochondrial Encephalomyopathy	44	0.087

38		HMP009	Haemophilus Influenzae	43	0.087

39	c	ATS307	Autosomal Recessive Cerebellar Ataxia	42	0.087

40		MTH072	Methemoglobin Reductase Deficiency	16	0.087

41	P	ALZ034	Alzheimer Disease	88	0.078

42	P	RSP003	Respiratory Failure	74	0.078

43	P	HYP061	Hypertrophic Cardiomyopathy	70	0.078

44	P	MYC084	Mycobacterium Tuberculosis 1	68	0.078

45	P	GLM045	Glioma	63	0.078

46		FTT001	Fatty Liver Disease	61	0.078

47		IRN002	Iron Metabolism Disease	57	0.078

48		GLL048	Glial Tumor	45	0.078

49		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.078

50		TRD008	Triiodothyronine Receptor Auxiliary Protein	34	0.078

51	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	90	0.067

52	P	OVR042	Ovarian Cancer	88	0.067

53	P	GST053	Gastric Cancer	83	0.067

54	P	HYP724	Hyperlipoproteinemia, Type Iii	73	0.067

55	P	LKM002	Leukemia	68	0.067

56	P	3MT016	3-Methylglutaconic Aciduria, Type Iii	67	0.067

57	P	DYS154	Dystonia	65	0.067

58		LSH001	Leishmaniasis	63	0.067

59		LPP008	Lipoprotein Quantitative Trait Locus	62	0.067

60	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	57	0.067

61	P	BPL003	Bipolar Disorder	56	0.067

62		ART140	Arteries, Anomalies of	52	0.067

63		DYS015	Dysentery	52	0.067

64		CRN030	Coronary Stenosis	50	0.067

65		BRN071	Brain Injury	49	0.067

66		ATS010	Autosomal Recessive Disease	48	0.067

67	P	KLZ004	Kala-Azar 1	41	0.067

68	c	MJR024	Major Affective Disorder 9	41	0.067

69	c	MJR022	Major Affective Disorder 8	38	0.067

70		MTC023	Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes	34	0.067

71		SCC003	Succinic Acidemia	10	0.067

72	P	CLR023	Colorectal Cancer	99	0.055

73		MLR004	Malaria	81	0.055

74	P	BLD134	Bladder Cancer	79	0.055

75		RNL114	Renal Cell Carcinoma, Nonpapillary	78	0.055

76	P	PRK057	Parkinson Disease, Late-Onset	78	0.055

77		CRV035	Cervical Cancer	76	0.055

78		PLM129	Pulmonary Disease, Chronic Obstructive	73	0.055

79	P	HNT016	Huntington Disease	72	0.055

80		DWN001	Down Syndrome	70	0.055

81		CRB037	Cerebral Palsy	69	0.055

82	P	HYP086	Hypothyroidism	69	0.055

83		CHL065	Cholangiocarcinoma	68	0.055

84	P	CRD119	Cardiac Arrest	67	0.055

85	P	CHR012	Chronic Granulomatous Disease	67	0.055

86		OST159	Osteogenic Sarcoma	66	0.055

87	P	MCR115	Microvascular Complications of Diabetes 5	66	0.055

88		ATH013	Atherosclerosis Susceptibility	65	0.055

89		NRM005	Neuromuscular Disease	64	0.055

90		TRN015	Transient Cerebral Ischemia	63	0.055

91	c	BRN108	Branchiootic Syndrome 1	62	0.055

92		DRM006	Dermatitis	61	0.055

93	P	MYL006	Myeloid Leukemia	60	0.055

94	P	CTR002	Cataract	60	0.055

95	P	BRS044	Breast Adenocarcinoma	59	0.055

96		CNT047	Contact Dermatitis	58	0.055

97	P	SZR006	Seizure Disorder	56	0.055

98		SLP001	Sleeping Sickness	54	0.055

99		DNT012	Dental Caries	53	0.055

100	P	SPP010	Suppressor of Tumorigenicity 3	51	0.055

101		INT079	Intrahepatic Cholangiocarcinoma	51	0.055

102		TRM010	Traumatic Brain Injury	51	0.055

103		CRV040	Cervix Carcinoma	51	0.055

104		RBF001	Riboflavin Deficiency	49	0.055

105	c	SPR009	Sporadic Breast Cancer	45	0.055

106		GRD001	Giardiasis	45	0.055

107	P	HYP265	Hypotonia	43	0.055

108		48X005	48,xyyy	39	0.055

109		ALL014	Allergic Encephalomyelitis	38	0.055

110		HRW001	Hair Whorl	36	0.055

111		PRM329	Premature Aging	35	0.055

112		CRT020	Cortisone Reductase Deficiency	31	0.055

113	c	THY056	Thyroid Dyshormonogenesis 3	30	0.055

114		PST092	Posttransplant Acute Limbic Encephalitis	29	0.055

115	P	HPT023	Hepatocellular Carcinoma	100	0.039

116		ESP021	Esophageal Cancer	90	0.039

117	c	AMY091	Amyotrophic Lateral Sclerosis 1	89	0.039

118	c	SYS001	Systemic Lupus Erythematosus	86	0.039

119	c	LKM061	Leukemia, Acute Myeloid	84	0.039

120	c	HYP595	Hypertension, Essential	84	0.039

121	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	81	0.039

122	c	DLT002	Dilated Cardiomyopathy	79	0.039

123		INS024	Insulin-Like Growth Factor I	79	0.039

124		GLB015	Glioblastoma Multiforme	75	0.039

125		SCK003	Sickle Cell Anemia	74	0.039

126		CRH001	Crohn's Disease	74	0.039

127	c	HYP836	Hypercholesterolemia, Familial, 1	73	0.039

128	c	HPT073	Hepatitis C Virus	72	0.039

129		OTT002	Otitis Media	72	0.039

130	P	PHC003	Pheochromocytoma	71	0.039

131		PRP027	Peripheral Vascular Disease	71	0.039

132	P	ATS364	Autism	70	0.039

133	c	CHR684	Chronic Kidney Disease	70	0.039

134	P	LPR021	Leprosy 3	69	0.039

135	P	LYM118	Lymphoma	68	0.039

136		BRK010	Burkitt Lymphoma	67	0.039

137		CRB039	Cerebrovascular Disease	67	0.039

138	P	BLD062	Bile Duct Cancer	67	0.039

139	P	MLG056	Malignant Hyperthermia	67	0.039

140	c	MGR028	Migraine with or Without Aura 1	67	0.039

141		ALC007	Alcohol Dependence	66	0.039

142		ANG054	Angina Pectoris	66	0.039

143	P	MSC005	Muscular Dystrophy	66	0.039

144		LBR036	Leber Plus Disease	66	0.039

145	P	HYD006	Hydrocephalus	66	0.039

146	P	DRM053	Dermatitis, Atopic	66	0.039

147	P	CCK001	Cockayne Syndrome	66	0.039

148		TTN003	Tetanus	65	0.039

149		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	65	0.039

150		PRT036	Peritonitis	64	0.039

151		MNK001	Menkes Disease	64	0.039

152		CTR172	Citrullinemia, Classic	64	0.039

153	P	FRD001	Friedreich Ataxia	64	0.039

154		ART002	Arts Syndrome	64	0.039

155		MSC007	Muscle Hypertrophy	64	0.039

156		KRN002	Kearns-Sayre Syndrome	63	0.039

157	c	PRC016	Pre-Eclampsia	63	0.039

158	P	CRN300	Coronary Heart Disease 1	63	0.039

159	P	END044	Endometriosis	63	0.039

160	c	ALP101	Alpha-Thalassemia	62	0.039

161	c	HPT001	Hepatitis C	62	0.039

162	P	PSR002	Psoriasis	62	0.039

163	P	MCH002	Machado-Joseph Disease	62	0.039

164	c	SVR001	Severe Acute Respiratory Syndrome	62	0.039

165	P	PRM006	Primary Biliary Cirrhosis	62	0.039

166		ASP002	Aspartylglucosaminuria	62	0.039

167	P	PRP029	Porphyria	62	0.039

168		NNL005	Non-Alcoholic Fatty Liver Disease	61	0.039

169		ARG002	Argininosuccinic Aciduria	61	0.039

170	P	LPS004	Lupus Erythematosus	61	0.039

171		PTN001	Patent Foramen Ovale	60	0.039

172		DBT084	Diabetes Mellitus, Ketosis-Prone	60	0.039

173	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	60	0.039

174		ORL011	Oral Cancer	60	0.039

175		INS001	Insulinoma	60	0.039

176	P	THL005	Thalassemia	60	0.039

177	P	MYC008	Myocarditis	59	0.039

178	P	MCR010	Microcephaly	59	0.039

179		CHL123	Chlamydia	59	0.039

180		VSL002	Visual Epilepsy	59	0.039

181	P	ANP001	Anaplastic Large Cell Lymphoma	58	0.039

182		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	0.039

183	P	INF032	Infertility	57	0.039

184	P	EXN002	Exanthem	57	0.039

185	P	END033	Endocarditis	57	0.039

186		TNS005	Tonsillitis	57	0.039

187		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	57	0.039

188	P	FBR017	Fibrosarcoma	56	0.039

189		ERY051	Erythroleukemia, Familial	56	0.039

190		ALL010	Allergic Contact Dermatitis	56	0.039

191		ANS011	Anus Cancer	56	0.039

192		AGN016	Aging	56	0.039

193	P	GST044	Gastritis	56	0.039

194	P	DRR001	Diarrhea	55	0.039

195		VSC003	Visceral Leishmaniasis	55	0.039

196	P	GRV001	Graves' Disease	55	0.039

197		FLR002	Filariasis	55	0.039

198	P	DBT005	Diabetes Insipidus	55	0.039

199	P	LRY044	Larynx Cancer	55	0.039

200	P	PRG130	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1	55	0.039

201		HYP060	Hyperinsulinism	54	0.039

202		RSC001	Rosacea	54	0.039

203		GLC003	Glucose Intolerance	54	0.039

204	P	LTR001	Lateral Sclerosis	54	0.039

205		HLL004	Hellp Syndrome	54	0.039

206	c	PRG040	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4	54	0.039

207		CLR030	Clear Cell Renal Cell Carcinoma	53	0.039

208		ECH003	Echinococcosis	53	0.039

209		INF034	Infective Endocarditis	53	0.039

210	P	PTS002	Ptosis	53	0.039

211		HMC014	Homocysteinemia	53	0.039

212	P	MYP087	Myopathy, Tubular Aggregate, 1	53	0.039

213	c	HYP807	Hyperinsulinemic Hypoglycemia, Familial, 6	52	0.039

214		PST011	Pustulosis of Palm and Sole	52	0.039

215	P	MSC003	Muscular Atrophy	52	0.039

216		GLC009	Glucosephosphate Dehydrogenase Deficiency	52	0.039

217		PTH003	Pathologic Nystagmus	52	0.039

218		HYP014	Hyperuricemia	52	0.039

219		APR001	Apraxia	52	0.039

220		ONC002	Onchocerciasis	52	0.039

221		OCL069	Ocular Motor Apraxia	51	0.039

222		HYP781	Hypoascorbemia	51	0.039

223		INT071	Intestinal Perforation	51	0.039

224	P	FNC004	Fanconi Syndrome	50	0.039

225		PRS034	Parasitic Helminthiasis Infectious Disease	50	0.039

226	P	ECL001	Eclampsia	50	0.039

227	c	PRG038	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2	50	0.039

228		MTB004	Metabolic Acidosis	50	0.039

229	P	MTH008	Methylmalonic Acidemia	50	0.039

230		DYS073	Dysphagia	50	0.039

231		VLV047	Volvulus of Midgut	49	0.039

232		ALV002	Alveolar Echinococcosis	49	0.039

233		47X002	47,xyy	49	0.039

234	P	CRV031	Cervical Adenocarcinoma	49	0.039

235		ATN005	Autonomic Dysfunction	46	0.039

236	P	BNG032	Benign Mesothelioma	46	0.039

237	c	CHR095	Chronic Progressive External Ophthalmoplegia	46	0.039

238	P	MYC033	Myoclonus	46	0.039

239	P	BRN006	Branchiootorenal Syndrome	46	0.039

240		HDN002	Head Injury	46	0.039

241		SNG007	Sengers Syndrome	46	0.039

242	c	MLG068	Malignant Glioma	46	0.039

243	c	EST002	Estrogen-Receptor Negative Breast Cancer	45	0.039

244		CRB004	Cerebral Artery Occlusion	45	0.039

245		LYD001	Leydig Cell Tumor	45	0.039

246		SPS007	Spastic Cerebral Palsy	45	0.039

247		CRT015	Carotid Artery Occlusion	45	0.039

248		SPS057	Spasticity	45	0.039

249		ATX038	Ataxia and Polyneuropathy, Adult-Onset	45	0.039

250		ORG002	Organic Acidemia	44	0.039

251		INT258	Interstitial Nephritis, Karyomegalic	44	0.039

252		CRB090	Cerebral Hypoxia	44	0.039

253	P	HRD018	Hair Disease	43	0.039

254		MST004	Mast Cell Neoplasm	42	0.039

255		KRT058	Keratoderma, Palmoplantar, with Deafness	42	0.039

256	c	BDY007	Body Mass Index Quantitative Trait Locus 1	42	0.039

257	P	RRT020	Rare Tumor	41	0.039

258	P	FNC034	Fanconi Renotubular Syndrome 2	40	0.039

259		SCR011	Scrapie	39	0.039

260		LBR031	Leber Optic Atrophy and Dystonia	38	0.039

261		EXT007	Extracutaneous Mastocytoma	38	0.039

262		PNB004	Panbronchiolitis, Diffuse	37	0.039

263		HMM004	Hamamy Syndrome	37	0.039

264		FST001	Foster-Kennedy Syndrome	36	0.039

265		MTH064	Methemoglobinemia, Beta-Globin Type	35	0.039

266		HNS001	Hansen's Disease	34	0.039

267	P	DFN349	Deafness, Nonsyndromic Sensorineural, Mitochondrial	34	0.039

268		CND006	Candida Glabrata	32	0.039

269		PRX097	Paroxysmal Dystonia	32	0.039

270		ALZ029	Alzheimer Disease Mitochondrial	32	0.039

271	c	DNT047	Dentinogenesis Imperfecta Type 2	31	0.039

272	c	THY071	Thyroid Dyshormonogenesis 1	31	0.039

273		RTN212	Retinal Dystrophy with or Without Macular Staphyloma	29	0.039

274		ISL099	Isolated Methylmalonic Acidemia	29	0.039

275		PLT031	Platelet Membrane Fluidity	29	0.039

276	c	RNG015	Ring Chromosome 2	26	0.039

277		STN013	Stenotrophomonas Maltophilia Infection	25	0.039

278		URT049	Urate Oxidase, Pseudogene	25	0.039

279		CNR001	Coenurosis	25	0.039

280		MTC015	Mitochondrial Dna-Associated Leigh Syndrome and Narp	24	0.039

281		CYN003	Cyanide Poisoning	24	0.039

282		PLG003	Polg-Related Disorders	24	0.039

283		HYP690	Hyper-Beta-Alaninemia	24	0.039

284		LCT008	Lactate Dehydrogenase Deficiency	19	0.039

285		PRS119	Persistent Genital Arousal Disorder	18	0.039

286		LTH004	Lathyrism	16	0.039

287		MYP161	Myopathy, Congenital Proximal, with Minicore Lesions	15	0.039

288		NNS010	Nonsyndromic Hearing Loss and Deafness, Mitochondrial	13	0.039

289		CNG393	Congenital Muscular Dystrophy with Hyperlaxity	12	0.039

290	c	LCT020	Lactic Acidosis, Chronic Adult Form	8	0.039