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
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