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
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
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