Search results for L-Carnitine

273 hits were found for L-Carnitine

# Family MCID Name MIFTS Score
1
P NRP001 Neuropathy 63 0.340
2
P LVR013 Liver Disease 75 0.323
3
P ENC018 Encephalopathy 62 0.323
4
PRP019 Peripheral Nervous System Disease 60 0.323
5
GST050 Gastrointestinal System Disease 64 0.304
6
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.294
7
P HPT021 Hepatitis 76 0.294
8
P KDN018 Kidney Disease 68 0.294
9
P NRV007 Nervous System Disease 73 0.284
10
NRM005 Neuromuscular Disease 60 0.284
11
URN009 Urinary System Disease 55 0.284
12
NRT004 Neuritis 57 0.274
13
c CNT035 Central Nervous System Disease 63 0.263
14
HPT019 Hepatic Encephalopathy 58 0.263
15
CRN239 Carnitine Deficiency, Systemic Primary 53 0.263
16
ART140 Arteries, Anomalies of 65 0.252
17
P VSC018 Visceral Steatosis 37 0.252
18
ISC004 Ischemia 65 0.240
19
c CHR089 Chronic Kidney Failure 72 0.228
20
DPR016 Depression 72 0.228
21
P MYP004 Myopathy 68 0.228
22
GST045 Gastroenteritis 64 0.228
23
P INT068 Intestinal Disease 64 0.228
24
END030 End Stage Renal Failure 56 0.228
25
P INF037 Inflammatory Bowel Disease 53 0.228
26
PRP080 Peripheral Artery Disease 53 0.228
27
P MSC033 Muscle Disorders 52 0.228
28
MSC004 Muscle Tissue Disease 39 0.228
29
VSC007 Vascular Disease 68 0.215
30
ACQ007 Acquired Immunodeficiency Syndrome 63 0.215
31
INT002 Intermittent Claudication 61 0.215
32
FTT001 Fatty Liver Disease 60 0.215
33
P ART021 Arteriosclerosis 60 0.215
34
MNT002 Mental Depression 57 0.215
35
TXC002 Toxic Encephalopathy 55 0.215
36
P ALZ034 Alzheimer Disease 87 0.201
37
ULC004 Ulcerative Colitis 72 0.201
38
PRP027 Peripheral Vascular Disease 70 0.201
39
AGN016 Aging 64 0.201
40
CLT003 Colitis 62 0.201
41
CLN019 Colonic Disease 54 0.201
42
c FTT008 Fatty Liver Disease, Nonalcoholic 1 39 0.201
43
c HPT001 Hepatitis C 71 0.186
44
P THL005 Thalassemia 64 0.186
45
P DBT009 Diabetes Mellitus 64 0.186
46
LPD008 Lipid Metabolism Disorder 58 0.186
47
HYP060 Hyperinsulinism 56 0.186
48
c ACT071 Acute Kidney Failure 54 0.186
49
SPN041 Spinal Cord Disease 51 0.186
50
ISV001 Isovaleric Acidemia 49 0.186
51
P BRS047 Breast Cancer 100 0.170
52
P MLT020 Multiple Sclerosis 78 0.170
53
c BTT014 Beta-Thalassemia 69 0.170
54
BRS051 Breast Disease 66 0.170
55
P INF032 Infertility 59 0.170
56
GLC003 Glucose Intolerance 56 0.170
57
SPS003 Spastic Diplegia 54 0.170
58
P NNL004 Nonalcoholic Fatty Liver Disease 51 0.170
59
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 29 0.170
60
P OVR042 Ovarian Cancer 81 0.152
61
P MYC007 Myocardial Infarction 79 0.152
62
P HRT032 Heart Disease 74 0.152
63
c HPT073 Hepatitis C Virus 72 0.152
64
P MPL001 Maple Syrup Urine Disease 65 0.152
65
P HYP086 Hypothyroidism 64 0.152
66
P PLY011 Polycystic Ovary Syndrome 63 0.152
67
PLC008 Placenta Disease 61 0.152
68
P PLY019 Polyneuropathy 57 0.152
69
BRN106 Burns 56 0.152
70
c PYR010 Peyronie's Disease 53 0.152
71
HMG005 Hemoglobinopathy 53 0.152
72
GLC008 Glucose Metabolism Disease 52 0.152
73
THY030 Thyroid Gland Disease 51 0.152
74
CYC008 Cyclic Vomiting Syndrome 49 0.152
75
CRH001 Crohn's Disease 78 0.132
76
CNG034 Congestive Heart Failure 72 0.132
77
ANX010 Anxiety 72 0.132
78
DMN002 Dementia 68 0.132
79
P SPN046 Spinal Muscular Atrophy 63 0.132
80
c OVR114 Ovarian Cancer 1 62 0.132
81
HYP056 Hypoglycemia 62 0.132
82
HYP266 Hypoxia 61 0.132
83
c HPT003 Hepatitis a 61 0.132
84
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 0.132
85
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 59 0.132
86
P MSC003 Muscular Atrophy 54 0.132
87
NNL002 Nonalcoholic Steatohepatitis 50 0.132
88
URT010 Ureteral Obstruction 48 0.132
89
P CNN004 Connective Tissue Cancer 45 0.132
90
END072 Endotheliitis 45 0.132
91
NRN002 Neuronitis 41 0.132
92
CRB009 Cerebritis 41 0.132
93
OVR094 Ovarian Epithelial Cancer 38 0.132
94
PRS063 Paresthesia 37 0.132
95
c PLY105 Polycystic Ovary Syndrome 1 30 0.132
96
P PRS040 Prostate Cancer 90 0.108
97
P OST002 Osteoporosis 76 0.108
98
GST019 Gastrointestinal Stromal Tumor 73 0.108
99
ACR006 Aceruloplasminemia 73 0.108
100
ISC006 Ischemic Heart Disease 72 0.108
101
BRC012 Brucellosis 70 0.108
102
P CRN018 Coronary Artery Anomaly 68 0.108
103
SPN186 Spinal Cord Injury 68 0.108
104
CRP001 Carpal Tunnel Syndrome 66 0.108
105
P CHR071 Charcot-Marie-Tooth Disease 65 0.108
106
c CRN300 Coronary Heart Disease 1 64 0.108
107
ATM095 Autoimmune Disease 64 0.108
108
GST092 Gastroesophageal Reflux 64 0.108
109
P FRD012 Friedreich Ataxia 1 64 0.108
110
HYP066 Hyperglycemia 63 0.108
111
RSP006 Respiratory System Disease 63 0.108
112
THR100 Thrombocytopenic Purpura, Autoimmune 62 0.108
113
HDC001 Headache 59 0.108
114
SLP005 Sleep Disorder 59 0.108
115
P OVR049 Ovarian Disease 59 0.108
116
PLM031 Poliomyelitis 58 0.108
117
c ACT075 Acute Myocardial Infarction 58 0.108
118
DMY004 Demyelinating Disease 57 0.108
119
PNC034 Pancreas Disease 57 0.108
120
c VSC019 Vesicoureteral Reflux 1 57 0.108
121
ILT001 Ileitis 56 0.108
122
URN010 Urinary Tract Obstruction 56 0.108
123
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 56 0.108
124
P PYL005 Pyelonephritis 56 0.108
125
P HYP076 Hyperthyroidism 56 0.108
126
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 55 0.108
127
AMN001 Amenorrhea 55 0.108
128
P ATS308 Autosomal Dominant Cerebellar Ataxia 54 0.108
129
c HYP795 Hypothyroidism, Congenital, Nongoitrous, 4 54 0.108
130
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 54 0.108
131
c INF071 Inflammatory Bowel Disease 1 53 0.108
132
TTH006 Tooth Disease 53 0.108
133
NRG002 Neurogenic Bladder 53 0.108
134
BRN071 Brain Injury 53 0.108
135
SNS003 Sensory Peripheral Neuropathy 53 0.108
136
MLN007 Male Infertility 53 0.108
137
MYL001 Myelitis 51 0.108
138
VRC001 Varicocele 51 0.108
139
INT067 Interstitial Nephritis 50 0.108
140
P LCT001 Lactic Acidosis 50 0.108
141
RYS001 Reye Syndrome 49 0.108
142
P MTC069 Mitochondrial Disorders 49 0.108
143
CRB027 Cerebellar Disease 49 0.108
144
c ACT042 Acute Pyelonephritis 46 0.108
145
RSS026 Roussy-Levy Hereditary Areflexic Dystasia 46 0.108
146
GND003 Gonadal Disease 46 0.108
147
c MTR002 Mitral Valve Insufficiency 46 0.108
148
OCL033 Oculocerebral Syndrome with Hypopigmentation 45 0.108
149
MNN017 Mononeuropathy 43 0.108
150
3MT001 3-Methylcrotonyl-Coa Carboxylase Deficiency 41 0.108
151
PST020 Postpoliomyelitis Syndrome 41 0.108
152
SPN050 Spinocerebellar Degeneration 40 0.108
153
MTR007 Motor Peripheral Neuropathy 40 0.108
154
PYL004 Pyelitis 37 0.108
155
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 36 0.108
156
NRV004 Nerve Compression Syndrome 35 0.108
157
MDN002 Median Neuropathy 32 0.108
158
P AST055 Asthma-Related Traits 1 30 0.108
159
URN022 Urinary Tract Infections, Recurrent 29 0.108
160
OVR077 Overuse Syndrome 24 0.108
161
P CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 23 0.108
162
RPT005 Repetitive Motion Disorders 23 0.108
163
SPN187 Spinocerebellar Atrophy 23 0.108
164
c VSC053 Visceral Steatosis, Congenital 21 0.108
165
CML001 Cumulative Trauma Disorders 21 0.108
166
ATR076 Atrophic Muscular Disease 18 0.108
167
CRN287 Carnitine Deficiency, Myopathic 17 0.108
168
PNC065 Pinched Nerve 16 0.108
169
RPT006 Repetitive Stress Injuries 16 0.108
170
P LNG032 Lung Cancer 98 0.076
171
AST005 Asthma 82 0.076
172
P RTT002 Rett Syndrome 82 0.076
173
P PNC035 Pancreatic Cancer 79 0.076
174
P ATX030 Ataxia-Telangiectasia 79 0.076
175
PLM129 Pulmonary Disease, Chronic Obstructive 72 0.076
176
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.076
177
LYM133 Lymphoma, Hodgkin, Classic 71 0.076
178
P LYM118 Lymphoma 70 0.076
179
MYL009 Myelodysplastic Syndrome 70 0.076
180
HMN044 Human Immunodeficiency Virus Type 1 70 0.076
181
P ADN016 Adenocarcinoma 70 0.076
182
P ATR011 Atrial Fibrillation 68 0.076
183
LVR012 Liver Cirrhosis 68 0.076
184
MSC157 Muscular Dystrophy, Duchenne Type 68 0.076
185
APN008 Apnea, Obstructive Sleep 67 0.076
186
LNG099 Lung Disease 67 0.076
187
SKN016 Skin Disease 66 0.076
188
P MSC005 Muscular Dystrophy 66 0.076
189
P SLP006 Sleep Apnea 66 0.076
190
END057 Endometrial Cancer 65 0.076
191
P END044 Endometriosis 64 0.076
192
P PNC044 Pancreatitis 64 0.076
193
MDD011 Mood Disorder 63 0.076
194
P NRC002 Narcolepsy 63 0.076
195
FLL027 Fallopian Tube Carcinoma 62 0.076
196
PRP001 Propionic Acidemia 62 0.076
197
P NRN021 Neuronal Ceroid Lipofuscinosis 61 0.076
198
P CMR001 Camurati-Engelmann Disease 61 0.076
199
P FBR017 Fibrosarcoma 61 0.076
200
ANR040 Aneurysm 60 0.076
201
c PRM126 Primary Peritoneal Carcinoma 60 0.076
202
P NPH012 Nephrotic Syndrome 59 0.076
203
P BPL003 Bipolar Disorder 59 0.076
204
c VRL010 Viral Hepatitis 59 0.076
205
P VNT002 Ventricular Septal Defect 58 0.076
206
P HYP069 Hyperparathyroidism 58 0.076
207
CRT049 Critical Limb Ischemia 57 0.076
208
P DRR001 Diarrhea 56 0.076
209
CNS004 Constipation 56 0.076
210
TYP041 Type I 56 0.076
211
P ATR001 Atrioventricular Septal Defect 56 0.076
212
PRN019 Perinatal Necrotizing Enterocolitis 56 0.076
213
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 56 0.076
214
P PMP005 Pemphigus Vulgaris 55 0.076
215
MTC027 Mitochondrial Trifunctional Protein Deficiency 54 0.076
216
P PMP001 Pemphigus 54 0.076
217
CYS014 Cystadenocarcinoma 54 0.076
218
DYS014 Dyspepsia 54 0.076
219
SRS001 Serous Cystadenocarcinoma 54 0.076
220
ENT011 Enterocolitis 54 0.076
221
GNR004 Generalized Anxiety Disorder 53 0.076
222
LYS003 Lysinuric Protein Intolerance 52 0.076
223
P FNC004 Fanconi Syndrome 52 0.076
224
MCN001 Mucinous Adenocarcinoma 52 0.076
225
URM002 Uremia 52 0.076
226
GRW007 Growth Hormone Deficiency 51 0.076
227
LMB062 Limb Ischemia 51 0.076
228
DBT004 Diabetic Polyneuropathy 51 0.076
229
RTN023 Retinitis 50 0.076
230
c SPN393 Spinal Muscular Atrophy, Type I 50 0.076
231
SCN001 Secondary Hyperparathyroidism of Renal Origin 50 0.076
232
HYP006 Hypertensive Heart Disease 50 0.076
233
RTN003 Retinal Ischemia 50 0.076
234
P OVR046 Ovarian Cyst 50 0.076
235
ANX004 Anoxia 49 0.076
236
c BPL002 Bipolar I Disorder 49 0.076
237
P BRN120 Bronchus Cancer 49 0.076
238
HYP458 Hyper Ige Syndrome 49 0.076
239
MTB004 Metabolic Acidosis 48 0.076
240
OVR012 Ovarian Serous Cystadenocarcinoma 48 0.076
241
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 48 0.076
242
SKN027 Skin Conditions 48 0.076
243
DBT008 Diabetic Angiopathy 47 0.076
244
ATN004 Autonomic Neuropathy 46 0.076
245
DST006 Diastolic Heart Failure 46 0.076
246
MYC072 Myoclonic Epilepsy Associated with Ragged-Red Fibers 45 0.076
247
P OVR010 Ovarian Brenner Tumor 44 0.076
248
c 3MT015 3-Methylglutaconic Aciduria, Type I 44 0.076
249
HRT011 Heart Septal Defect 43 0.076
250
c L2H001 L-2-Hydroxyglutaric Aciduria 42 0.076
251
URM005 Uremic Pruritus 42 0.076
252
PRT035 Peritoneum Cancer 42 0.076
253
MCN008 Mucinous Cystadenocarcinoma 41 0.076
254
ALC010 Alcoholic Cardiomyopathy 41 0.076
255
3HY007 3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency 41 0.076
256
RBF001 Riboflavin Deficiency 41 0.076
257
OLG001 Oligospermia 40 0.076
258
PHT003 Phototoxic Dermatitis 40 0.076
259
HYP064 Hypogonadotropism 40 0.076
260
BTN004 Biotin Deficiency 37 0.076
261
TXC020 Toxic Oil Syndrome 36 0.076
262
FLL029 Fallopian Tube Disease 35 0.076
263
OVR013 Ovarian Mucinous Cystadenocarcinoma 33 0.076
264
CHL045 Choline Deficiency Disease 33 0.076
265
CMP035 Complete Atrioventricular Canal 30 0.076
266
c PMP006 Pemphigus Vulgaris, Familial 28 0.076
267
ISB001 Isobutyryl-Coa Dehydrogenase Deficiency 27 0.076
268
MTH079 Methylmalonic Acidemia and Homocysteinemia, Cblx Type 22 0.076
269
BRN126 Brenner Tumor of Ovary 20 0.076
270
MLG035 Malignant Ovarian Mixed Epithelial Neoplasm 16 0.076
271
OVR022 Ovary Mixed Epithelial Carcinoma 15 0.076
272
OVR040 Ovarian Clear Cell Cystadenocarcinoma 15 0.076
273
MXD024 Mixed Epithelial Tumor of Ovary 14 0.076
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