Search results for Clofibrate

244 hits were found for Clofibrate

# Family MCID Name MIFTS Score
1
P DBT005 Diabetes Insipidus 55 0.249
2
c HYP836 Hypercholesterolemia, Familial, 1 73 0.204
3
P HYP750 Hypertriglyceridemia, Familial 62 0.201
4
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.184
5
P HRT032 Heart Disease 75 0.176
6
BLR008 Bilirubin Metabolic Disorder 57 0.162
7
P MYP004 Myopathy 70 0.152
8
P DBT009 Diabetes Mellitus 64 0.147
9
P CRN300 Coronary Heart Disease 1 63 0.147
10
P VSC007 Vascular Disease 63 0.136
11
P ART021 Arteriosclerosis 54 0.136
12
P KDN018 Kidney Disease 72 0.130
13
ATH013 Atherosclerosis Susceptibility 65 0.130
14
c FML021 Familial Hypercholesterolemia 66 0.118
15
P MCR115 Microvascular Complications of Diabetes 5 66 0.111
16
MYT011 Myotonia 34 0.111
17
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.104
18
P MYC007 Myocardial Infarction 70 0.104
19
c GLL024 Gallbladder Disease 1 53 0.104
20
48X005 48,xyyy 39 0.104
21
PPL052 Papillomatosis, Confluent and Reticulated 33 0.104
22
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.096
23
LPP008 Lipoprotein Quantitative Trait Locus 62 0.096
24
LVR012 Liver Cirrhosis 62 0.096
25
FTT001 Fatty Liver Disease 61 0.096
26
NNT012 Neonatal Jaundice 53 0.096
27
P HYP086 Hypothyroidism 69 0.088
28
LPD008 Lipid Metabolism Disorder 62 0.088
29
P NPH012 Nephrotic Syndrome 60 0.088
30
P CRD246 Cardiovascular System Disease 57 0.088
31
ANG054 Angina Pectoris 66 0.079
32
ISC004 Ischemia 58 0.079
33
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.079
34
P NRP001 Neuropathy 56 0.079
35
HYP014 Hyperuricemia 52 0.079
36
XNT003 Xanthomatosis 49 0.079
37
CHL004 Cholelithiasis 49 0.079
38
P KRN004 Kernicterus 47 0.079
39
ADR007 Adrenoleukodystrophy 75 0.068
40
PRP027 Peripheral Vascular Disease 71 0.068
41
P HYP098 Hypereosinophilic Syndrome 67 0.068
42
P PRM006 Primary Biliary Cirrhosis 62 0.068
43
CHL068 Cholestasis 61 0.068
44
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.068
45
c FML035 Familial Hyperlipidemia 55 0.068
46
HYP060 Hyperinsulinism 54 0.068
47
GLC003 Glucose Intolerance 54 0.068
48
DBT010 Diabetic Neuropathy 54 0.068
49
ART140 Arteries, Anomalies of 52 0.068
50
P CRC039 Coarctation of Aorta 47 0.068
51
ATX019 Ataxia with Vitamin E Deficiency 42 0.068
52
ADR022 Adrenomyeloneuropathy 38 0.068
53
c HNT011 Huntington Disease-Like 3 38 0.068
54
P HPT023 Hepatocellular Carcinoma 100 0.056
55
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.056
56
P OVR042 Ovarian Cancer 88 0.056
57
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.056
58
c LKM063 Leukemia, Chronic Myeloid 72 0.056
59
P LVR013 Liver Disease 68 0.056
60
P HPT021 Hepatitis 67 0.056
61
CRB039 Cerebrovascular Disease 67 0.056
62
HYP056 Hypoglycemia 66 0.056
63
P ADN016 Adenocarcinoma 64 0.056
64
INT002 Intermittent Claudication 61 0.056
65
P MYL006 Myeloid Leukemia 60 0.056
66
c ACT027 Acute Pancreatitis 60 0.056
67
c ACT071 Acute Kidney Failure 60 0.056
68
ADN018 Adenoma 59 0.056
69
ERY003 Erythema Multiforme 58 0.056
70
EYD002 Eye Disease 58 0.056
71
P GLL020 Gallbladder Disease 57 0.056
72
P ZLL001 Zellweger Syndrome 57 0.056
73
P HYP076 Hyperthyroidism 55 0.056
74
IMP005 Impotence 52 0.056
75
HPT014 Hepatorenal Syndrome 50 0.056
76
47X002 47,xyy 49 0.056
77
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.056
78
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.056
79
P CLR023 Colorectal Cancer 99 0.039
80
P BRS047 Breast Cancer 97 0.039
81
MYL069 Myeloma, Multiple 85 0.039
82
c HYP595 Hypertension, Essential 84 0.039
83
P PNC035 Pancreatic Cancer 84 0.039
84
IMM167 Immune Deficiency Disease 78 0.039
85
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.039
86
c ATR087 Atrial Standstill 1 75 0.039
87
LPT014 Leptin Deficiency or Dysfunction 74 0.039
88
c SPN225 Spondyloarthropathy 1 73 0.039
89
P FML018 Familial Mediterranean Fever 73 0.039
90
HMN044 Human Immunodeficiency Virus Type 1 71 0.039
91
DFC004 Deficiency Anemia 70 0.039
92
P AMY004 Amyloidosis 70 0.039
93
MYL009 Myelodysplastic Syndrome 70 0.039
94
LGH007 Leigh Syndrome 70 0.039
95
CNG034 Congestive Heart Failure 69 0.039
96
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.039
97
P ART022 Arthritis 69 0.039
98
SVR097 Severe Cutaneous Adverse Reaction 69 0.039
99
P SLP006 Sleep Apnea 69 0.039
100
P PNM007 Pneumonia 68 0.039
101
P TRN020 Turner Syndrome 67 0.039
102
c MCR129 Microvascular Complications of Diabetes 1 66 0.039
103
P ATR011 Atrial Fibrillation 66 0.039
104
P DRM053 Dermatitis, Atopic 66 0.039
105
c FML001 Familial Atrial Fibrillation 65 0.039
106
TNG002 Tangier Disease 65 0.039
107
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.039
108
P HRP006 Herpes Simplex 65 0.039
109
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.039
110
CLN015 Colon Adenocarcinoma 65 0.039
111
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.039
112
APN008 Apnea, Obstructive Sleep 64 0.039
113
BRC012 Brucellosis 64 0.039
114
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.039
115
c ATS013 Autosomal Recessive Congenital Ichthyosis 63 0.039
116
KRN002 Kearns-Sayre Syndrome 63 0.039
117
c ACT068 Acute Cystitis 63 0.039
118
c ATM011 Autoimmune Hepatitis 63 0.039
119
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.039
120
P PSR002 Psoriasis 62 0.039
121
c HPT003 Hepatitis a 62 0.039
122
c BRN108 Branchiootic Syndrome 1 62 0.039
123
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.039
124
ALL026 Allergic Hypersensitivity Disease 62 0.039
125
CRC021 Carcinosarcoma 62 0.039
126
NTR005 Nutritional Deficiency Disease 62 0.039
127
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.039
128
HYP066 Hyperglycemia 61 0.039
129
CHN055 Chanarin-Dorfman Syndrome 61 0.039
130
DRM006 Dermatitis 61 0.039
131
P ENC018 Encephalopathy 61 0.039
132
P PNC044 Pancreatitis 61 0.039
133
P LPS004 Lupus Erythematosus 61 0.039
134
HPT019 Hepatic Encephalopathy 60 0.039
135
ACQ007 Acquired Immunodeficiency Syndrome 60 0.039
136
P BND020 Bone Disease 59 0.039
137
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.039
138
DBT087 Diabetes Insipidus, Neurohypophyseal 58 0.039
139
GLB001 Gilbert Syndrome 58 0.039
140
P ALC033 Alcohol Use Disorder 58 0.039
141
BRG013 Buerger Disease 58 0.039
142
P GLM007 Glomerulonephritis 57 0.039
143
c CHL119 Cholangitis, Primary Sclerosing 57 0.039
144
P PLY041 Polymyositis 57 0.039
145
DSS009 Disseminated Intravascular Coagulation 57 0.039
146
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.039
147
c ACT075 Acute Myocardial Infarction 57 0.039
148
THR024 Thrombosis 57 0.039
149
P PYL005 Pyelonephritis 56 0.039
150
P MYS005 Myositis 56 0.039
151
P MTC069 Mitochondrial Disorders 56 0.039
152
NRL004 Neuroleptic Malignant Syndrome 56 0.039
153
P HYP838 Hyperlipidemia, Familial Combined, 3 56 0.039
154
AGN016 Aging 56 0.039
155
P GST044 Gastritis 56 0.039
156
HYP005 Hypokalemia 55 0.039
157
MCL006 Macular Retinal Edema 55 0.039
158
P DRR001 Diarrhea 55 0.039
159
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.039
160
P PTT006 Pituitary Adenoma 55 0.039
161
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.039
162
ANL018 Analbuminemia 54 0.039
163
PPL022 Papilloma 54 0.039
164
TRC023 Trichinosis 53 0.039
165
P HYP083 Hypopituitarism 53 0.039
166
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.039
167
PRP080 Peripheral Artery Disease 53 0.039
168
P RTN018 Retinal Disease 53 0.039
169
c MCR113 Microvascular Complications of Diabetes 3 52 0.039
170
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.039
171
PST011 Pustulosis of Palm and Sole 52 0.039
172
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.039
173
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.039
174
c HYP843 Hypoalphalipoproteinemia, Primary, 2 52 0.039
175
LMY002 Leiomyoma 52 0.039
176
SPN051 Spondylitis 51 0.039
177
THR016 Thrombophlebitis 51 0.039
178
LNG031 Lung Benign Neoplasm 51 0.039
179
END086 End Stage Renal Disease 51 0.039
180
P CHL066 Cholangitis 51 0.039
181
HYP081 Hypolipoproteinemia 51 0.039
182
c HNT004 Huntington Disease-Like 2 50 0.039
183
P ESN008 Eosinophilic Pneumonia 50 0.039
184
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.039
185
c HYP739 Hyperlipoproteinemia, Type Iv 50 0.039
186
RBF001 Riboflavin Deficiency 49 0.039
187
P MYT002 Myotonic Dystrophy 49 0.039
188
P MTC133 Mitochondrial Myopathy 49 0.039
189
P OPN001 Open-Angle Glaucoma 49 0.039
190
MTC005 Mitochondrial Metabolism Disease 49 0.039
191
URM002 Uremia 49 0.039
192
VCC001 Vaccinia 49 0.039
193
ATS010 Autosomal Recessive Disease 48 0.039
194
P SCL009 Sclerosing Cholangitis 48 0.039
195
INT067 Interstitial Nephritis 48 0.039
196
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.039
197
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.039
198
THY128 Thyroid Tumor 47 0.039
199
c MCR120 Microvascular Complications of Diabetes 7 47 0.039
200
c INH020 Inherited Metabolic Disorder 47 0.039
201
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.039
202
LPD009 Lipid Storage Disease 46 0.039
203
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.039
204
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.039
205
SQM002 Squamous Cell Papilloma 46 0.039
206
PRX001 Peroxisomal Disease 46 0.039
207
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.039
208
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.039
209
HPT004 Hepatic Coma 45 0.039
210
FSH001 Fish-Eye Disease 45 0.039
211
ORG002 Organic Acidemia 44 0.039
212
c HYP272 Hypercholesterolemia, Familial, 3 44 0.039
213
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.039
214
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.039
215
P MYG005 Myoglobinuria 44 0.039
216
P HYP121 Hypoalphalipoproteinemia 43 0.039
217
c ICH049 Ichthyosis, Congenital, Autosomal Recessive 2 43 0.039
218
MNN017 Mononeuropathy 42 0.039
219
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.039
220
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.039
221
c SZR022 Seizures, Benign Familial Neonatal, 1 42 0.039
222
c HYP841 Hypoalphalipoproteinemia, Primary, 1 41 0.039
223
NTR007 Neutral Lipid Storage Disease with Myopathy 41 0.039
224
c MCR130 Microvascular Complications of Diabetes 6 41 0.039
225
c MCR133 Microvascular Complications of Diabetes 4 41 0.039
226
c MCR112 Microvascular Complications of Diabetes 2 41 0.039
227
PYL004 Pyelitis 40 0.039
228
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.039
229
MSC190 Muscular Disease 37 0.039
230
GRN009 Granulomatous Hepatitis 33 0.039
231
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.039
232
KDN013 Kidney Hypertrophy 32 0.039
233
INF009 Inflammatory Spondylopathy 31 0.039
234
SPR017 Spermatocele 31 0.039
235
LCH014 Lichen Amyloidosis 31 0.039
236
ERY066 Erythema Multiforme Major 30 0.039
237
c BLR024 Biliary Cirrhosis, Primary, 1 30 0.039
238
ANG037 Angiomatosis 28 0.039
239
c RNG015 Ring Chromosome 2 26 0.039
240
STN013 Stenotrophomonas Maltophilia Infection 25 0.039
241
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.039
242
URT049 Urate Oxidase, Pseudogene 25 0.039
243
DPS001 Dipsogenic Diabetes Insipidus 23 0.039
244
ORN004 Ornithinemia 17 0.039
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