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
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
Content
Loading form....