Search results for Fenofibrate

363 hits were found for Fenofibrate

# Family MCID Name MIFTS Score
1
LPD008 Lipid Metabolism Disorder 64 0.655
2
P HYP750 Hypertriglyceridemia, Familial 62 0.497
3
c HYP836 Hypercholesterolemia, Familial, 1 74 0.358
4
c HYP555 Hypertriglyceridemia, Transient Infantile 38 0.324
5
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.305
6
c FML035 Familial Hyperlipidemia 56 0.301
7
HYP081 Hypolipoproteinemia 51 0.277
8
OBS529 Obsolete: Combined Hyperlipidemia 22 0.270
9
P MCR115 Microvascular Complications of Diabetes 5 67 0.264
10
P CRN300 Coronary Heart Disease 1 59 0.240
11
P DBT009 Diabetes Mellitus 66 0.238
12
P TRN020 Turner Syndrome 66 0.233
13
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 54 0.230
14
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.228
15
P CRN018 Coronary Artery Anomaly 67 0.228
16
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.212
17
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.212
18
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.209
19
FTT001 Fatty Liver Disease 63 0.206
20
ADL002 Adult Syndrome 62 0.206
21
c HYP740 Hyperlipoproteinemia, Type V 53 0.206
22
c HYP272 Hypercholesterolemia, Familial, 3 44 0.203
23
P LVR013 Liver Disease 71 0.200
24
ATH013 Atherosclerosis Susceptibility 68 0.191
25
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.191
26
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.191
27
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.191
28
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.191
29
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.191
30
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.191
31
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.191
32
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.191
33
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.191
34
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.191
35
ISC004 Ischemia 62 0.185
36
P MYP004 Myopathy 63 0.182
37
c MCR113 Microvascular Complications of Diabetes 3 55 0.182
38
c MCR120 Microvascular Complications of Diabetes 7 48 0.182
39
c MCR130 Microvascular Complications of Diabetes 6 42 0.182
40
c MCR133 Microvascular Complications of Diabetes 4 42 0.182
41
P KDN018 Kidney Disease 73 0.178
42
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.178
43
ART140 Arteries, Anomalies of 60 0.178
44
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.178
45
P HRT032 Heart Disease 78 0.175
46
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.172
47
P HYP838 Hyperlipidemia, Familial Combined, 3 54 0.172
48
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.172
49
PRM236 Primary Biliary Cholangitis 57 0.168
50
P PRM006 Primary Biliary Cirrhosis 54 0.157
51
LVR012 Liver Cirrhosis 67 0.153
52
HYP066 Hyperglycemia 63 0.153
53
c HYP839 Hyperlipidemia, Familial Combined, 1 28 0.150
54
c FML021 Familial Hypercholesterolemia 67 0.146
55
48X005 48,xyyy 37 0.146
56
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.137
57
c MCR129 Microvascular Complications of Diabetes 1 67 0.133
58
HYP060 Hyperinsulinism 55 0.128
59
NNL006 Non-Alcoholic Steatohepatitis 53 0.128
60
GLB002 Glioblastoma 74 0.124
61
GLB015 Glioblastoma Multiforme 60 0.124
62
c MCR112 Microvascular Complications of Diabetes 2 42 0.124
63
CRB039 Cerebrovascular Disease 71 0.119
64
GT001 Gout 63 0.119
65
P CHL066 Cholangitis 53 0.119
66
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.119
67
c BLR024 Biliary Cirrhosis, Primary, 1 30 0.114
68
P VSC007 Vascular Disease 65 0.109
69
c RHB024 Rhabdomyosarcoma 2 64 0.109
70
CHL068 Cholestasis 61 0.109
71
c ACT071 Acute Kidney Failure 60 0.109
72
P EXN002 Exanthem 58 0.109
73
HMN014 Human Immunodeficiency Virus Infectious Disease 56 0.109
74
MCL006 Macular Retinal Edema 52 0.109
75
c HYP595 Hypertension, Essential 87 0.103
76
P MYC007 Myocardial Infarction 74 0.103
77
P HYP086 Hypothyroidism 70 0.103
78
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 63 0.103
79
P RTN018 Retinal Disease 53 0.103
80
LPD009 Lipid Storage Disease 49 0.103
81
GLC008 Glucose Metabolism Disease 47 0.103
82
FML235 Familial Combined Hyperlipoproteinemia 29 0.103
83
STR067 Stroke, Ischemic 82 0.097
84
c CHR684 Chronic Kidney Disease 68 0.097
85
P ART021 Arteriosclerosis 56 0.097
86
c HYP768 Hyperlipoproteinemia, Type I 50 0.097
87
DBT006 Diabetic Macular Edema 46 0.097
88
DWN001 Down Syndrome 70 0.091
89
P HPT021 Hepatitis 69 0.091
90
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.091
91
P PNC044 Pancreatitis 61 0.091
92
END030 End Stage Renal Failure 60 0.091
93
GLC003 Glucose Intolerance 55 0.091
94
ATX019 Ataxia with Vitamin E Deficiency 46 0.091
95
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 44 0.091
96
P VSC018 Visceral Steatosis 34 0.091
97
LPT014 Leptin Deficiency or Dysfunction 72 0.084
98
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.084
99
P SCL009 Sclerosing Cholangitis 47 0.084
100
CYT002 Cytokine Deficiency 46 0.084
101
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.084
102
CYT018 Cytochrome P450 2d6 Variant 28 0.084
103
MYL069 Myeloma, Multiple 85 0.077
104
P MDL005 Medulloblastoma 78 0.077
105
c ATR087 Atrial Standstill 1 76 0.077
106
HMN044 Human Immunodeficiency Virus Type 1 73 0.077
107
CNG034 Congestive Heart Failure 69 0.077
108
HYP056 Hypoglycemia 68 0.077
109
P NRB010 Neuroblastoma 1 66 0.077
110
c FNC043 Fanconi Anemia, Complementation Group E 64 0.077
111
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 62 0.077
112
P MYC008 Myocarditis 60 0.077
113
THR024 Thrombosis 58 0.077
114
HYP005 Hypokalemia 55 0.077
115
HMC014 Homocysteinemia 54 0.077
116
P MYS005 Myositis 54 0.077
117
IMP005 Impotence 53 0.077
118
HYP014 Hyperuricemia 52 0.077
119
c HNT011 Huntington Disease-Like 3 37 0.077
120
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 36 0.077
121
P PRS040 Prostate Cancer 97 0.069
122
IMM167 Immune Deficiency Disease 79 0.069
123
PRP027 Peripheral Vascular Disease 72 0.069
124
ART016 Aortic Aneurysm 71 0.069
125
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.069
126
INC002 Inclusion Body Myositis 66 0.069
127
SPN186 Spinal Cord Injury 63 0.069
128
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.069
129
c ART138 Aortic Aneurysm, Familial Abdominal, 1 62 0.069
130
ORL011 Oral Cancer 62 0.069
131
c CHL119 Cholangitis, Primary Sclerosing 59 0.069
132
P PLY011 Polycystic Ovary Syndrome 58 0.069
133
P ALC033 Alcohol Use Disorder 58 0.069
134
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.069
135
c HYP841 Hypoalphalipoproteinemia, Primary, 1 53 0.069
136
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.069
137
P MSC003 Muscular Atrophy 52 0.069
138
CHL004 Cholelithiasis 50 0.069
139
P IDP024 Idiopathic Inflammatory Myopathy 49 0.069
140
SXL003 Sexual Disorder 49 0.069
141
RTN020 Retinal Vascular Disease 49 0.069
142
47X002 47,xyy 49 0.069
143
GLL048 Glial Tumor 48 0.069
144
CRB004 Cerebral Artery Occlusion 38 0.069
145
c BNG079 Benign Adult Familial Myoclonic Epilepsy 36 0.069
146
c CHR682 Chronic Bilirubin Encephalopathy 36 0.069
147
P OVR096 Overlap Myositis 28 0.069
148
P HPT023 Hepatocellular Carcinoma 99 0.059
149
P LNG032 Lung Cancer 99 0.059
150
P CNR004 Cone-Rod Dystrophy 2 72 0.059
151
P HNT016 Huntington Disease 72 0.059
152
P SLP006 Sleep Apnea 71 0.059
153
P LYM118 Lymphoma 70 0.059
154
P LKM002 Leukemia 69 0.059
155
EWN003 Ewing Sarcoma 69 0.059
156
ANG054 Angina Pectoris 66 0.059
157
HMT002 Hematologic Cancer 64 0.059
158
APN008 Apnea, Obstructive Sleep 64 0.059
159
P GLM045 Glioma 64 0.059
160
P EPN002 Ependymoma 61 0.059
161
NTR005 Nutritional Deficiency Disease 61 0.059
162
EYD002 Eye Disease 59 0.059
163
P HDC001 Headache 59 0.059
164
c ACT075 Acute Myocardial Infarction 59 0.059
165
BCT022 Bacterial Infectious Disease 57 0.059
166
P PLY041 Polymyositis 57 0.059
167
P NRV006 Nervous System Cancer 55 0.059
168
TRM010 Traumatic Brain Injury 54 0.059
169
PRP016 Paraplegia 54 0.059
170
c GLL024 Gallbladder Disease 1 53 0.059
171
c CNT033 Central Nervous System Cancer 51 0.059
172
QDR001 Quadriplegia 51 0.059
173
BRN071 Brain Injury 51 0.059
174
CRN030 Coronary Stenosis 49 0.059
175
c BNG030 Benign Ependymoma 48 0.059
176
LYM019 Lymphosarcoma 48 0.059
177
HMZ003 Homozygous Familial Hypercholesterolemia 48 0.059
178
PNC119 Pancreatic Neuroendocrine Tumor 48 0.059
179
MCL027 Macular Dystrophy, Dominant Cystoid 47 0.059
180
KRT013 Keratolytic Winter Erythema 45 0.059
181
LKS001 Leukostasis 43 0.059
182
TRP009 Triple X Syndrome 42 0.059
183
c PLY105 Polycystic Ovary Syndrome 1 38 0.059
184
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 32 0.059
185
CRT084 Creatinine Clearance Quantitative Trait Locus 26 0.059
186
c HYP163 Hyperlipidemia Type 3 23 0.059
188
P PNC035 Pancreatic Cancer 86 0.049
189
P RHM011 Rheumatoid Arthritis 82 0.049
190
P SCH015 Schizophrenia 76 0.049
191
BRN028 Brain Cancer 75 0.049
192
ANX010 Anxiety 75 0.049
193
P RTN024 Retinoblastoma 74 0.049
194
ADR007 Adrenoleukodystrophy 72 0.049
195
ALC007 Alcohol Dependence 68 0.049
196
MLN008 Melanoma 68 0.049
197
P NPH012 Nephrotic Syndrome 65 0.049
198
TNG002 Tangier Disease 64 0.049
199
CLT003 Colitis 63 0.049
200
LNG099 Lung Disease 62 0.049
201
ATM095 Autoimmune Disease 62 0.049
202
SQM006 Squamous Cell Carcinoma 60 0.049
203
c ACT027 Acute Pancreatitis 60 0.049
204
ANR040 Aneurysm 60 0.049
205
CHL123 Chlamydia 60 0.049
206
INS001 Insulinoma 60 0.049
207
AGN016 Aging 58 0.049
208
INT007 Intermediate Coronary Syndrome 58 0.049
209
P NRP001 Neuropathy 57 0.049
210
ALL006 Allergic Asthma 56 0.049
211
PRD004 Prediabetes Syndrome 49 0.049
212
MTB004 Metabolic Acidosis 48 0.049
213
c HNT004 Huntington Disease-Like 2 48 0.049
214
c FML008 Familial Retinoblastoma 46 0.049
215
c PRM038 Primary Agammaglobulinemia 45 0.049
216
DST006 Diastolic Heart Failure 43 0.049
217
ADR022 Adrenomyeloneuropathy 39 0.049
218
CHL147 Chlamydia Pneumonia 39 0.049
219
c ATM022 Autoimmune Myocarditis 36 0.049
220
c HYP843 Hypoalphalipoproteinemia, Primary, 2 29 0.049
221
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 0.049
222
SLN001 Silent Myocardial Infarction 26 0.049
223
P ALZ034 Alzheimer Disease 90 0.034
224
ESP021 Esophageal Cancer 90 0.034
225
P OVR042 Ovarian Cancer 89 0.034
226
CYS001 Cystic Fibrosis 84 0.034
227
c DLT002 Dilated Cardiomyopathy 81 0.034
228
AST005 Asthma 80 0.034
229
OST012 Osteoarthritis 80 0.034
230
INS024 Insulin-Like Growth Factor I 79 0.034
231
P LNG064 Lung Cancer Susceptibility 3 79 0.034
232
CNN003 Conn's Syndrome 78 0.034
233
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.034
234
CRH001 Crohn's Disease 75 0.034
235
END057 Endometrial Cancer 74 0.034
236
c HPT073 Hepatitis C Virus 74 0.034
237
c LKM063 Leukemia, Chronic Myeloid 74 0.034
238
P EPL164 Epilepsy 73 0.034
239
P MLT020 Multiple Sclerosis 73 0.034
240
P AMY004 Amyloidosis 71 0.034
241
P ART022 Arthritis 71 0.034
242
BRN024 Bronchitis 70 0.034
243
c EXD008 Exudative Vitreoretinopathy 1 69 0.034
244
c ATS007 Autism Spectrum Disorder 69 0.034
245
MNT001 Mantle Cell Lymphoma 69 0.034
246
P PLM037 Pulmonary Hypertension 69 0.034
247
P ATS364 Autism 68 0.034
248
P ATR011 Atrial Fibrillation 67 0.034
249
P HYP098 Hypereosinophilic Syndrome 67 0.034
250
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.034
251
P THR014 Thrombocytopenia 67 0.034
252
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.034
253
c SML038 Small Cell Cancer of the Lung 67 0.034
254
MYC006 Mycosis Fungoides 67 0.034
255
P PLM036 Pulmonary Fibrosis 66 0.034
256
CHG001 Chagas Disease 66 0.034
257
CRN036 Craniopharyngioma 65 0.034
258
P ADN016 Adenocarcinoma 65 0.034
259
ALL026 Allergic Hypersensitivity Disease 65 0.034
260
IDP011 Idiopathic Interstitial Pneumonia 65 0.034
261
P PRP019 Peripheral Nervous System Disease 64 0.034
262
P VSC011 Vasculitis 64 0.034
263
P ENC004 Encephalitis 64 0.034
264
P NTR004 Neutropenia 64 0.034
265
DRM006 Dermatitis 63 0.034
266
c ATM011 Autoimmune Hepatitis 63 0.034
267
P NRN021 Neuronal Ceroid Lipofuscinosis 63 0.034
268
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 63 0.034
269
P END044 Endometriosis 63 0.034
270
MCR013 Microphthalmia 62 0.034
271
HYP020 Hyperprolactinemia 62 0.034
272
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.034
273
P CRG003 Crigler-Najjar Syndrome, Type I 61 0.034
274
STT001 Status Epilepticus 61 0.034
275
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.034
276
P BCL017 B-Cell Lymphoma 61 0.034
277
c NMN016 Niemann-Pick Disease, Type B 61 0.034
278
P PLY014 Polycystic Kidney Disease 61 0.034
279
P NMN002 Niemann-Pick Disease 60 0.034
280
BND020 Bone Disease 60 0.034
281
PLM033 Pulmonary Embolism 60 0.034
282
ADN018 Adenoma 60 0.034
283
ANG020 Angiosarcoma 59 0.034
284
CNS004 Constipation 59 0.034
285
c ACT210 Acute Respiratory Distress Syndrome 59 0.034
286
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 58 0.034
287
P ALP008 Alopecia 58 0.034
288
HYP266 Hypoxia 58 0.034
289
LYM027 Lymphopenia 58 0.034
290
BLR008 Bilirubin Metabolic Disorder 58 0.034
291
P INF037 Inflammatory Bowel Disease 57 0.034
292
BRN004 Brain Edema 57 0.034
293
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.034
294
c SVR001 Severe Acute Respiratory Syndrome 56 0.034
295
FCL014 Focal Epilepsy 56 0.034
296
DBT010 Diabetic Neuropathy 56 0.034
297
JPN002 Japanese Encephalitis 56 0.034
298
SNS003 Sensory Peripheral Neuropathy 56 0.034
299
GRN034 Grange Syndrome 55 0.034
300
P LCH002 Lichen Planus 55 0.034
301
P PLY019 Polyneuropathy 55 0.034
302
PRS045 Prostatic Hypertrophy 55 0.034
303
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 54 0.034
304
PLG002 Plague 54 0.034
305
PNC001 Pancytopenia 54 0.034
306
P LCT001 Lactic Acidosis 52 0.034
307
PRS021 Prostatic Adenoma 52 0.034
308
DYS014 Dyspepsia 51 0.034
309
CLR109 Colorectal Adenocarcinoma 51 0.034
310
BNR002 Bone Resorption Disease 51 0.034
311
IMM064 Immunodeficiency, Common Variable, 10 51 0.034
312
HYP080 Hypogonadism 51 0.034
313
LMB062 Limb Ischemia 50 0.034
314
c AMY009 Amyloidosis Aa 50 0.034
315
MLT134 Multiple Pterygium Syndrome, Lethal Type 50 0.034
316
c VRL007 Viral Encephalitis 49 0.034
317
PRS129 Prostatic Hyperplasia, Benign 49 0.034
318
HYP006 Hypertensive Heart Disease 49 0.034
319
HMG002 Hemoglobinuria 49 0.034
320
P RNV001 Renovascular Hypertension 49 0.034
321
ATS010 Autosomal Recessive Disease 49 0.034
322
RNL077 Renal Fibrosis 49 0.034
323
P HYP121 Hypoalphalipoproteinemia 49 0.034
324
GYN001 Gynecomastia 49 0.034
325
CRN027 Corneal Neovascularization 48 0.034
326
P ATS011 Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 48 0.034
327
c CRG004 Crigler-Najjar Syndrome, Type Ii 48 0.034
328
HPT025 Hepatic Lipase Deficiency 47 0.034
329
P ART018 Aortic Valve Insufficiency 47 0.034
330
c MLG069 Malignant Hypertension 46 0.034
331
c MLG068 Malignant Glioma 46 0.034
332
PLT004 Platelet Glycoprotein Iv Deficiency 45 0.034
333
HPT067 Hepatocellular Adenoma 45 0.034
334
MYC005 Myocardial Stunning 45 0.034
335
KHN001 Kuhnt-Junius Degeneration 45 0.034
336
ORL015 Oral Squamous Cell Carcinoma 44 0.034
337
LPP002 Lipoprotein Glomerulopathy 44 0.034
338
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 44 0.034
339
c PCH010 Pachyonychia Congenita 3 43 0.034
340
SYS003 Systolic Heart Failure 43 0.034
341
PRS042 Prostate Disease 42 0.034
342
ACT003 Acute Kidney Tubular Necrosis 42 0.034
343
DRG002 Drug-Induced Hepatitis 41 0.034
344
NSP002 Nasopharyngitis 41 0.034
345
CNT060 Central Serous Chorioretinopathy 41 0.034
346
PLY100 Polyploidy 41 0.034
347
ALL014 Allergic Encephalomyelitis 40 0.034
348
HPT082 Hepatic Adenomas, Familial 40 0.034
349
HYP064 Hypogonadotropism 40 0.034
350
PLT015 Platelet Aggregation, Spontaneous 40 0.034
351
ACT167 Acute Generalized Exanthematous Pustulosis 38 0.034
352
BCK003 Background Diabetic Retinopathy 37 0.034
353
HRW001 Hair Whorl 36 0.034
354
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.034
356
PPL052 Papillomatosis, Confluent and Reticulated 34 0.034
357
CGH001 Cough Variant Asthma 34 0.034
358
INF021 Infant Gynecomastia 32 0.034
359
PLY150 Polykaryocytosis Inducer 31 0.034
360
GNT019 Giant Cell Myocarditis 30 0.034
361
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 29 0.034
362
URT049 Urate Oxidase, Pseudogene 26 0.034
363
c CRN175 Coronary Heart Disease 4 13 0.034
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