Search results for NADH

295 hits were found for NADH

#	Family	MCID	Name	MIFTS	Score
1		MTC146	Mitochondrial Complex I Deficiency, Nuclear Type 1	57	10.360

2		MTH026	Methemoglobinemia Due to Deficiency of Methemoglobin Reductase	36	8.957

3		OBS421	Obsolete: Fatal Infantile Hypertrophic Cardiomyopathy Due to Mitochondrial Complex I Deficiency	5	3.182

4	P	OBS124	Obsolete: Recessive Hereditary Methemoglobinemia Type 1	4	3.182

5	c	OBS125	Obsolete: Recessive Hereditary Methemoglobinemia Type 2	4	3.182

6	P	MPL001	Maple Syrup Urine Disease	68	2.250

7		PYR031	Pyruvate Dehydrogenase E3-Binding Protein Deficiency	40	2.250

8		DHY010	Dihydrolipoamide Dehydrogenase Deficiency	39	2.250

9	P	MTH007	Methemoglobinemia	47	0.352

10	c	HRD146	Hereditary Methemoglobinemia	29	0.301

11	c	CNG223	Congenital Methemoglobinemia	25	0.220

12	P	MTC069	Mitochondrial Disorders	57	0.206

13		ANX004	Anoxia	44	0.194

14	P	MYP004	Myopathy	63	0.177

15	P	LCT001	Lactic Acidosis	52	0.173

16		MTC005	Mitochondrial Metabolism Disease	50	0.168

17	P	MTC133	Mitochondrial Myopathy	53	0.163

18		CYN002	Cyanosis, Transient Neonatal	45	0.153

19		HYP266	Hypoxia	58	0.148

20		LGH007	Leigh Syndrome	69	0.143

21	P	OPT006	Optic Nerve Disease	59	0.143

22	P	HRD217	Hereditary Optic Neuropathy	35	0.143

23		LBR030	Leber Optic Atrophy	61	0.125

24	P	NRB010	Neuroblastoma 1	66	0.119

25	P	ENC018	Encephalopathy	64	0.119

26		ISC004	Ischemia	62	0.119

27	P	NRP001	Neuropathy	57	0.112

28		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.112

29	c	ATR087	Atrial Standstill 1	76	0.105

30		CHG001	Chagas Disease	66	0.105

31		CHL014	Cholera	58	0.105

32		HLX001	Helix Syndrome	46	0.105

33		HYP056	Hypoglycemia	68	0.097

34	P	VSC007	Vascular Disease	65	0.097

35		CHR066	Chronic Fatigue Syndrome	61	0.097

36		TRD008	Triiodothyronine Receptor Auxiliary Protein	35	0.097

37	P	BRS047	Breast Cancer	99	0.089

38	P	ALZ034	Alzheimer Disease	90	0.089

39		CYS001	Cystic Fibrosis	84	0.089

40		PRT037	Pertussis	66	0.089

41		HYP066	Hyperglycemia	63	0.089

42		MTC114	Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes	58	0.089

43		HMP009	Haemophilus Influenzae	46	0.089

44		MTC004	Mitochondrial Encephalomyopathy	44	0.089

45	c	ATS307	Autosomal Recessive Cerebellar Ataxia	44	0.089

46		MTH072	Methemoglobin Reductase Deficiency	19	0.089

47	P	GST053	Gastric Cancer	85	0.079

48	P	RSP003	Respiratory Failure	75	0.079

49	P	MYC084	Mycobacterium Tuberculosis 1	69	0.079

50	P	HYP061	Hypertrophic Cardiomyopathy	68	0.079

51		LPD008	Lipid Metabolism Disorder	64	0.079

52		IRN002	Iron Metabolism Disease	58	0.079

53	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	91	0.069

54	P	OVR042	Ovarian Cancer	89	0.069

55	P	HYP724	Hyperlipoproteinemia, Type Iii	74	0.069

56	P	LKM002	Leukemia	69	0.069

57		ATH013	Atherosclerosis Susceptibility	68	0.069

58	P	CRN018	Coronary Artery Anomaly	67	0.069

59	P	DYS154	Dystonia	65	0.069

60	P	3MT016	3-Methylglutaconic Aciduria, Type Iii	64	0.069

61		LSH001	Leishmaniasis	64	0.069

62	P	GLM045	Glioma	64	0.069

63		FTT001	Fatty Liver Disease	63	0.069

64		ART140	Arteries, Anomalies of	60	0.069

65	P	BPL003	Bipolar Disorder	59	0.069

66	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	59	0.069

67		BRN071	Brain Injury	51	0.069

68		CRN030	Coronary Stenosis	49	0.069

69		ATS010	Autosomal Recessive Disease	49	0.069

70		47X002	47,xyy	49	0.069

71		GLL048	Glial Tumor	48	0.069

72		DYS015	Dysentery	45	0.069

73	P	KLZ004	Kala-Azar 1	43	0.069

74	c	MJR024	Major Affective Disorder 9	42	0.069

75	c	MJR022	Major Affective Disorder 8	39	0.069

76		MTC023	Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes	36	0.069

77		SCC003	Succinic Acidemia	10	0.069

78	P	CLR023	Colorectal Cancer	100	0.056

79	P	BLD134	Bladder Cancer	79	0.056

80		CRV035	Cervical Cancer	77	0.056

81	P	PRK057	Parkinson Disease, Late-Onset	77	0.056

82		PLM129	Pulmonary Disease, Chronic Obstructive	74	0.056

83	c	LKM063	Leukemia, Chronic Myeloid	74	0.056

84	P	EPL164	Epilepsy	73	0.056

85	P	HNT016	Huntington Disease	72	0.056

86	P	CRD119	Cardiac Arrest	71	0.056

87	P	HYP086	Hypothyroidism	70	0.056

88		DWN001	Down Syndrome	70	0.056

89		CRB037	Cerebral Palsy	69	0.056

90	P	CHR012	Chronic Granulomatous Disease	69	0.056

91		CHL065	Cholangiocarcinoma	68	0.056

92	P	MCR115	Microvascular Complications of Diabetes 5	67	0.056

93		OST159	Osteogenic Sarcoma	67	0.056

94		DRM006	Dermatitis	63	0.056

95	c	BRN108	Branchiootic Syndrome 1	62	0.056

96		NRM005	Neuromuscular Disease	62	0.056

97		TRN015	Transient Cerebral Ischemia	62	0.056

98	P	CTR002	Cataract	62	0.056

99	P	SZR006	Seizure Disorder	59	0.056

100	P	BRS044	Breast Adenocarcinoma	59	0.056

101		OBS525	Obsolete: Squamous Cell Carcinoma of Head and Neck	58	0.056

102		CNT047	Contact Dermatitis	58	0.056

103		TRM010	Traumatic Brain Injury	54	0.056

104		INT079	Intrahepatic Cholangiocarcinoma	54	0.056

105		SPP010	Suppressor of Tumorigenicity 3	54	0.056

106		DNT012	Dental Caries	52	0.056

107		CRV040	Cervix Carcinoma	52	0.056

108		SLP001	Sleeping Sickness	47	0.056

109		RBF001	Riboflavin Deficiency	46	0.056

110	c	SPR009	Sporadic Breast Cancer	45	0.056

111	P	HYP265	Hypotonia	43	0.056

112		GRD001	Giardiasis	42	0.056

113		PRM329	Premature Aging	41	0.056

114		48X005	48,xyyy	37	0.056

115		HRW001	Hair Whorl	36	0.056

116		CRT020	Cortisone Reductase Deficiency	35	0.056

117		PST092	Posttransplant Acute Limbic Encephalitis	29	0.056

118	c	THY056	Thyroid Dyshormonogenesis 3	28	0.056

119		TRY004	Trypanosomiasis, Human East-African	25	0.056

120	P	HPT023	Hepatocellular Carcinoma	99	0.040

121		ESP021	Esophageal Cancer	90	0.040

122	c	AMY091	Amyotrophic Lateral Sclerosis 1	88	0.040

123	c	HYP595	Hypertension, Essential	87	0.040

124	c	LKM061	Leukemia, Acute Myeloid	84	0.040

125	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	82	0.040

126		MLR004	Malaria	82	0.040

127	c	DLT002	Dilated Cardiomyopathy	81	0.040

128		INS024	Insulin-Like Growth Factor I	79	0.040

129		RNL114	Renal Cell Carcinoma, Nonpapillary	79	0.040

130	P	SCH015	Schizophrenia	76	0.040

131		CRH001	Crohn's Disease	75	0.040

132		SCK003	Sickle Cell Anemia	74	0.040

133	c	HPT073	Hepatitis C Virus	74	0.040

134	c	HYP836	Hypercholesterolemia, Familial, 1	74	0.040

135		PRP027	Peripheral Vascular Disease	72	0.040

136		OTT002	Otitis Media	71	0.040

137	P	PHC003	Pheochromocytoma	71	0.040

138	c	MGR028	Migraine with or Without Aura 1	70	0.040

139	P	LYM118	Lymphoma	70	0.040

140	P	ATS364	Autism	68	0.040

141	c	CHR684	Chronic Kidney Disease	68	0.040

142	P	HYD006	Hydrocephalus	68	0.040

143		ALC007	Alcohol Dependence	68	0.040

144		BRK010	Burkitt Lymphoma	68	0.040

145		MLN008	Melanoma	68	0.040

146	P	MSC005	Muscular Dystrophy	68	0.040

147	P	DRM053	Dermatitis, Atopic	68	0.040

148	P	LPR021	Leprosy 3	67	0.040

149	P	LBR001	Leber Congenital Amaurosis	67	0.040

150	P	DBT009	Diabetes Mellitus	66	0.040

151		PRT036	Peritonitis	66	0.040

152	P	BLD062	Bile Duct Cancer	66	0.040

153		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	0.040

154		ANG054	Angina Pectoris	66	0.040

155	P	CCK001	Cockayne Syndrome	66	0.040

156		MSC007	Muscle Hypertrophy	65	0.040

157	P	FRD012	Friedreich Ataxia 1	65	0.040

158		KRN002	Kearns-Sayre Syndrome	64	0.040

159	P	PSR002	Psoriasis	63	0.040

160	c	PRC016	Pre-Eclampsia	63	0.040

161	c	ALP101	Alpha-Thalassemia	63	0.040

162	P	END044	Endometriosis	63	0.040

163		MNK001	Menkes Disease	62	0.040

164	P	THL005	Thalassemia	62	0.040

165		TTN003	Tetanus	62	0.040

166		CTR172	Citrullinemia, Classic	62	0.040

167	c	HPT001	Hepatitis C	62	0.040

168		ORL011	Oral Cancer	62	0.040

169	P	MCH002	Machado-Joseph Disease	61	0.040

170	P	MYL006	Myeloid Leukemia	61	0.040

171	P	MYC008	Myocarditis	60	0.040

172		DBT084	Diabetes Mellitus, Ketosis-Prone	60	0.040

173		INS001	Insulinoma	60	0.040

174	P	MLG056	Malignant Hyperthermia	60	0.040

175	P	INF032	Infertility	60	0.040

176	P	CRN300	Coronary Heart Disease 1	59	0.040

177		ARG002	Argininosuccinic Aciduria	59	0.040

178	P	LRY044	Larynx Cancer	59	0.040

179		VSL002	Visual Epilepsy	58	0.040

180	P	PRP029	Porphyria	58	0.040

181	P	END033	Endocarditis	58	0.040

182		ERY051	Erythroleukemia, Familial	58	0.040

183		AGN016	Aging	58	0.040

184		TNS005	Tonsillitis	58	0.040

185	P	GST044	Gastritis	58	0.040

186		PRM236	Primary Biliary Cholangitis	57	0.040

187	P	FBR017	Fibrosarcoma	57	0.040

188	P	GRV001	Graves' Disease	57	0.040

189		PTN001	Patent Foramen Ovale	57	0.040

190		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	57	0.040

191		ALL010	Allergic Contact Dermatitis	56	0.040

192		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	56	0.040

193	P	MCR010	Microcephaly	56	0.040

194		FLR002	Filariasis	56	0.040

195	c	SVR001	Severe Acute Respiratory Syndrome	56	0.040

196	P	LTR001	Lateral Sclerosis	56	0.040

197	c	CNG216	Congenital Hydrocephalus	55	0.040

198		ASP002	Aspartylglucosaminuria	55	0.040

199	P	DRR001	Diarrhea	55	0.040

200		GLC003	Glucose Intolerance	55	0.040

201		VSC003	Visceral Leishmaniasis	55	0.040

202	P	OPT009	Optic Neuritis	55	0.040

203		RSC001	Rosacea	55	0.040

204	P	PRM006	Primary Biliary Cirrhosis	54	0.040

205	P	DBT005	Diabetes Insipidus	54	0.040

206		HMC014	Homocysteinemia	54	0.040

207		CLR030	Clear Cell Renal Cell Carcinoma	54	0.040

208		ECH003	Echinococcosis	54	0.040

209		MSC190	Muscular Disease	54	0.040

210		INF034	Infective Endocarditis	53	0.040

211		PTH003	Pathologic Nystagmus	53	0.040

212	P	PTS002	Ptosis	53	0.040

213		HLL004	Hellp Syndrome	53	0.040

214	P	ECL001	Eclampsia	53	0.040

215		OCL069	Ocular Motor Apraxia	53	0.040

216		DYS073	Dysphagia	52	0.040

217		HYP014	Hyperuricemia	52	0.040

218	P	MYP087	Myopathy, Tubular Aggregate, 1	52	0.040

219		GLC009	Glucosephosphate Dehydrogenase Deficiency	52	0.040

220		NRT004	Neuritis	52	0.040

221	P	MSC003	Muscular Atrophy	52	0.040

222		PRN011	Pernicious Anemia	51	0.040

223		ATX038	Ataxia and Polyneuropathy, Adult-Onset	51	0.040

224		IMM064	Immunodeficiency, Common Variable, 10	51	0.040

225		PST011	Pustulosis of Palm and Sole	51	0.040

226		APR001	Apraxia	50	0.040

227		ONC002	Onchocerciasis	50	0.040

228		ALV002	Alveolar Echinococcosis	50	0.040

229	P	MTH008	Methylmalonic Acidemia	50	0.040

230		ANS011	Anus Cancer	49	0.040

231	P	CRV031	Cervical Adenocarcinoma	49	0.040

232		MTB004	Metabolic Acidosis	48	0.040

233		HYP781	Hypoascorbemia	48	0.040

234		PRS034	Parasitic Helminthiasis Infectious Disease	48	0.040

235		ATN005	Autonomic Dysfunction	48	0.040

236	P	FNC004	Fanconi Syndrome	48	0.040

237	P	MYC033	Myoclonus	47	0.040

238	P	BNG032	Benign Mesothelioma	47	0.040

239		HDN002	Head Injury	47	0.040

240	c	MLG068	Malignant Glioma	46	0.040

241	c	CHR095	Chronic Progressive External Ophthalmoplegia	46	0.040

242		INT071	Intestinal Perforation	45	0.040

243		CRB090	Cerebral Hypoxia	45	0.040

244	P	LYD001	Leydig Cell Tumor	45	0.040

245		SPS007	Spastic Cerebral Palsy	45	0.040

246	P	BRN006	Branchiootorenal Syndrome	44	0.040

247		CRT015	Carotid Artery Occlusion	44	0.040

248		INT052	Intestinal Volvulus	44	0.040

249	c	BDY007	Body Mass Index Quantitative Trait Locus 1	43	0.040

250	c	EST002	Estrogen-Receptor Negative Breast Cancer	43	0.040

251	c	PRG130	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1	43	0.040

252	P	HRD018	Hair Disease	43	0.040

253	c	PRG039	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3	43	0.040

254		ORG002	Organic Acidemia	43	0.040

255	c	PRG040	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4	40	0.040

256		ALL014	Allergic Encephalomyelitis	40	0.040

257		MST004	Mast Cell Neoplasm	40	0.040

258		INT258	Interstitial Nephritis, Karyomegalic	40	0.040

259	c	PRG038	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2	40	0.040

260		FST001	Foster-Kennedy Syndrome	40	0.040

261		SNG007	Sengers Syndrome	39	0.040

262		EXT007	Extracutaneous Mastocytoma	39	0.040

263		CRB004	Cerebral Artery Occlusion	38	0.040

264		MTH064	Methemoglobinemia, Beta-Globin Type	37	0.040

265		PNB004	Panbronchiolitis, Diffuse	37	0.040

266		SCR011	Scrapie	37	0.040

267		LBR031	Leber Optic Atrophy and Dystonia	36	0.040

268		HMM004	Hamamy Syndrome	36	0.040

269		HNS001	Hansen's Disease	35	0.040

270	c	DNT047	Dentinogenesis Imperfecta Type 2	34	0.040

271		CND006	Candida Glabrata	33	0.040

272	P	DFN349	Deafness, Nonsyndromic Sensorineural, Mitochondrial	33	0.040

273		KRT058	Keratoderma, Palmoplantar, with Deafness	32	0.040

274		PRX097	Paroxysmal Dystonia	31	0.040

275		ISL099	Isolated Methylmalonic Acidemia	30	0.040

276		HMG010	Hemoglobinemia	29	0.040

277		ALZ029	Alzheimer Disease Mitochondrial	29	0.040

278		PLT031	Platelet Membrane Fluidity	29	0.040

279		RTN212	Retinal Dystrophy with or Without Macular Staphyloma	29	0.040

280		CNR001	Coenurosis	29	0.040

281	c	THY071	Thyroid Dyshormonogenesis 1	28	0.040

282	c	RNG015	Ring Chromosome 2	27	0.040

283		MTC015	Mitochondrial Dna-Associated Leigh Syndrome and Narp	27	0.040

284		STN013	Stenotrophomonas Maltophilia Infection	26	0.040

285		URT049	Urate Oxidase, Pseudogene	26	0.040

286		CYN003	Cyanide Poisoning	24	0.040

287		PLG003	Polg-Related Disorders	24	0.040

288		HYP690	Hyper-Beta-Alaninemia	22	0.040

289		MTC106	Mitochondrial Non-Syndromic Sensorineural Deafness	19	0.040

290		PRS119	Persistent Genital Arousal Disorder	19	0.040

291		LTH004	Lathyrism	16	0.040

292		LCT008	Lactate Dehydrogenase Deficiency	16	0.040

293		NNS010	Nonsyndromic Hearing Loss and Deafness, Mitochondrial	13	0.040

294		CNG393	Congenital Muscular Dystrophy with Hyperlaxity	12	0.040

295	c	LCT020	Lactic Acidosis, Chronic Adult Form	8	0.040