Search results for Cilostazol

266 hits were found for Cilostazol

# Family MCID Name MIFTS Score
1
INT002 Intermittent Claudication 61 0.485
2
PRP027 Peripheral Vascular Disease 71 0.405
3
ISC004 Ischemia 58 0.363
4
STR067 Stroke, Ischemic 81 0.321
5
ART140 Arteries, Anomalies of 52 0.317
6
CRB039 Cerebrovascular Disease 67 0.310
7
PRP080 Peripheral Artery Disease 53 0.307
8
P VSC007 Vascular Disease 63 0.293
9
LPP008 Lipoprotein Quantitative Trait Locus 62 0.247
10
ATH013 Atherosclerosis Susceptibility 65 0.229
11
P MYC007 Myocardial Infarction 70 0.212
12
P CRN300 Coronary Heart Disease 1 63 0.212
13
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.209
14
LMB062 Limb Ischemia 55 0.194
15
P HDC001 Headache 57 0.191
16
P ART021 Arteriosclerosis 54 0.187
17
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.183
18
c ACT075 Acute Myocardial Infarction 57 0.179
19
THR024 Thrombosis 57 0.170
20
c MGR028 Migraine with or Without Aura 1 67 0.166
21
P DMN002 Dementia 66 0.166
22
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.162
23
P ALZ034 Alzheimer Disease 88 0.152
24
P DBT009 Diabetes Mellitus 64 0.152
25
P TRN020 Turner Syndrome 67 0.148
26
ANG054 Angina Pectoris 66 0.148
27
KHL003 Kohlschutter-Tonz Syndrome 65 0.148
28
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.148
29
P CRD246 Cardiovascular System Disease 57 0.143
30
c MCR113 Microvascular Complications of Diabetes 3 52 0.143
31
c MCR120 Microvascular Complications of Diabetes 7 47 0.143
32
c MCR130 Microvascular Complications of Diabetes 6 41 0.143
33
c MCR133 Microvascular Complications of Diabetes 4 41 0.143
34
ART008 Arteriosclerosis Obliterans 40 0.143
35
P KDN018 Kidney Disease 72 0.137
36
LPD008 Lipid Metabolism Disorder 62 0.137
37
ADL002 Adult Syndrome 70 0.132
38
P MCR115 Microvascular Complications of Diabetes 5 66 0.132
39
CRT013 Carotid Stenosis 50 0.132
40
CRB004 Cerebral Artery Occlusion 45 0.132
41
CLP006 Clopidogrel Resistance 40 0.132
42
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.126
43
P NRP001 Neuropathy 56 0.126
44
P EXN002 Exanthem 57 0.120
45
VSC002 Vascular Dementia 57 0.120
46
CRN030 Coronary Stenosis 50 0.120
47
P MGR001 Migraine Without Aura 49 0.120
48
P HRT032 Heart Disease 75 0.114
49
TRN015 Transient Cerebral Ischemia 63 0.114
50
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.114
51
HMR039 Hemorrhage, Intracerebral 57 0.114
52
48X005 48,xyyy 39 0.114
53
DWN001 Down Syndrome 70 0.108
54
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.108
55
DPR016 Depression 63 0.108
56
P DRR001 Diarrhea 55 0.108
57
DBT010 Diabetic Neuropathy 54 0.108
58
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.108
59
GSG001 Gas Gangrene 53 0.108
60
CYT002 Cytokine Deficiency 42 0.108
61
c HYP836 Hypercholesterolemia, Familial, 1 73 0.101
62
P BRG001 Brugada Syndrome 71 0.101
63
HYP066 Hyperglycemia 61 0.101
64
ANR040 Aneurysm 59 0.101
65
MNT002 Mental Depression 58 0.101
66
CRT015 Carotid Artery Occlusion 45 0.101
67
c HYP595 Hypertension, Essential 84 0.093
68
c CHR684 Chronic Kidney Disease 70 0.093
69
c MCR129 Microvascular Complications of Diabetes 1 66 0.093
70
P SCK002 Sick Sinus Syndrome 55 0.093
71
CRT016 Carotid Artery Disease 52 0.093
72
CRB008 Cerebral Atherosclerosis 44 0.093
73
c MCR112 Microvascular Complications of Diabetes 2 41 0.093
74
ASP030 Aspirin Resistance 39 0.093
75
INT074 Intracranial Arteriosclerosis 23 0.093
76
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.085
77
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.085
78
CNG034 Congestive Heart Failure 69 0.085
79
P MJR001 Major Depressive Disorder 68 0.085
80
BRG013 Buerger Disease 58 0.085
81
ATR057 Atrioventricular Block 55 0.085
82
INT007 Intermediate Coronary Syndrome 55 0.085
83
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.085
84
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.085
85
END086 End Stage Renal Disease 51 0.085
86
BRN071 Brain Injury 49 0.085
87
INT010 Intracranial Embolism 48 0.085
88
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.085
89
CRN017 Coronary Thrombosis 47 0.085
90
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.085
91
RYN005 Raynaud Phenomenon 47 0.085
92
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.085
93
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.085
94
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.085
95
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.085
96
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.085
97
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.085
98
P PNM007 Pneumonia 68 0.076
99
P ATR011 Atrial Fibrillation 66 0.076
100
P NTR004 Neutropenia 63 0.076
101
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.076
102
CRD132 Cardiac Conduction Defect 58 0.076
103
HYP266 Hypoxia 57 0.076
104
INT030 Intracranial Aneurysm 56 0.076
105
P PLY019 Polyneuropathy 56 0.076
106
ACT058 Active Peptic Ulcer Disease 55 0.076
107
DBT004 Diabetic Polyneuropathy 49 0.076
108
47X002 47,xyy 49 0.076
109
SYN036 Syncope 45 0.076
110
CRB086 Cerebral Aneurysms 40 0.076
111
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.076
112
c SYS001 Systemic Lupus Erythematosus 86 0.066
113
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.066
114
ANX010 Anxiety 73 0.066
115
P NRB001 Neuroblastoma 72 0.066
116
HMN044 Human Immunodeficiency Virus Type 1 71 0.066
117
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.066
118
P SYS005 Systemic Scleroderma 68 0.066
119
CNN005 Connective Tissue Disease 68 0.066
120
P THR014 Thrombocytopenia 67 0.066
121
c RHB024 Rhabdomyosarcoma 2 67 0.066
122
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.066
123
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.066
124
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.066
125
CLT003 Colitis 62 0.066
126
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.066
127
FTT001 Fatty Liver Disease 61 0.066
128
P LPS004 Lupus Erythematosus 61 0.066
129
ACQ007 Acquired Immunodeficiency Syndrome 60 0.066
130
P PRP019 Peripheral Nervous System Disease 58 0.066
131
c FML035 Familial Hyperlipidemia 55 0.066
132
END040 Endogenous Depression 55 0.066
133
PRP030 Purpura 54 0.066
134
NRT001 Neurotic Disorder 53 0.066
135
P MGR003 Migraine with Aura 52 0.066
136
HYP081 Hypolipoproteinemia 51 0.066
137
RTN003 Retinal Ischemia 50 0.066
138
INT078 Intracranial Thrombosis 49 0.066
139
RYN001 Raynaud Disease 48 0.066
140
RTN020 Retinal Vascular Disease 46 0.066
141
c HYP272 Hypercholesterolemia, Familial, 3 44 0.066
142
TRP009 Triple X Syndrome 42 0.066
143
P INT260 Intracranial Berry Aneurysm 39 0.066
144
P CRN133 Coronary Artery Disease, Autosomal Dominant, 1 32 0.066
145
P CLR023 Colorectal Cancer 99 0.054
146
P RHM011 Rheumatoid Arthritis 80 0.054
147
INS024 Insulin-Like Growth Factor I 79 0.054
148
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.054
149
APR006 Apert Syndrome 70 0.054
150
ART016 Aortic Aneurysm 69 0.054
151
P TMP003 Temporal Arteritis 68 0.054
152
P HYD006 Hydrocephalus 66 0.054
153
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.054
154
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.054
155
SPN186 Spinal Cord Injury 60 0.054
156
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.054
157
SPN027 Spinal Stenosis 59 0.054
158
PPT005 Peptic Ulcer Disease 59 0.054
159
MXD005 Mixed Connective Tissue Disease 58 0.054
160
IRN002 Iron Metabolism Disease 57 0.054
161
P MYM013 Moyamoya Disease 1 57 0.054
162
P RHN004 Rhinitis 57 0.054
163
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.054
164
CMR002 Coumarin Resistance 56 0.054
165
HYP060 Hyperinsulinism 54 0.054
166
CYN002 Cyanosis, Transient Neonatal 45 0.054
167
CNT017 Central Nervous System Origin Vertigo 45 0.054
168
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.054
169
ALL014 Allergic Encephalomyelitis 38 0.054
170
PRP028 Peripheral Vertigo 37 0.054
171
c VRL004 Viral Labyrinthitis 35 0.054
172
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.054
173
VST001 Vestibular Neuronitis 34 0.054
174
NRN002 Neuronitis 32 0.054
175
CRC034 Carcinoma Showing Thymus-Like Differentiation 23 0.054
176
ERL052 Early Repolarization Associated with Ventricular Fibrillation 22 0.054
177
CRB087 Cerebral Arteriosclerosis 22 0.054
178
MNS002 Mini Stroke 19 0.054
179
P GLM040 Glioma Susceptibility 1 81 0.038
180
c DLT002 Dilated Cardiomyopathy 79 0.038
181
GST019 Gastrointestinal Stromal Tumor 78 0.038
182
OST012 Osteoarthritis 78 0.038
183
AST005 Asthma 76 0.038
184
c ATR087 Atrial Standstill 1 75 0.038
185
CRH001 Crohn's Disease 74 0.038
186
MSC157 Muscular Dystrophy, Duchenne Type 72 0.038
187
P HNT016 Huntington Disease 72 0.038
188
P PHC003 Pheochromocytoma 71 0.038
189
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.038
190
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.038
191
P LVR013 Liver Disease 68 0.038
192
P HYP098 Hypereosinophilic Syndrome 67 0.038
193
P MSC005 Muscular Dystrophy 66 0.038
194
c FML001 Familial Atrial Fibrillation 65 0.038
195
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.038
196
P ADN016 Adenocarcinoma 64 0.038
197
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.038
198
P PLY014 Polycystic Kidney Disease 62 0.038
199
P HYP750 Hypertriglyceridemia, Familial 62 0.038
200
ALL026 Allergic Hypersensitivity Disease 62 0.038
201
MDD011 Mood Disorder 62 0.038
202
CHL068 Cholestasis 61 0.038
204
c SCL052 Scleroderma, Familial Progressive 61 0.038
205
ALC006 Alcoholic Hepatitis 61 0.038
206
c ACT027 Acute Pancreatitis 60 0.038
207
CRD223 Cardiac Arrhythmia 60 0.038
208
c ACT071 Acute Kidney Failure 60 0.038
209
P MYC008 Myocarditis 59 0.038
210
PRT013 Portal Hypertension 59 0.038
211
PLM033 Pulmonary Embolism 59 0.038
212
P BCL017 B-Cell Lymphoma 58 0.038
213
P ALC033 Alcohol Use Disorder 58 0.038
214
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.038
215
MCR013 Microphthalmia 57 0.038
216
CHL067 Cholecystitis 57 0.038
217
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.038
218
CRT033 Corticobasal Degeneration 57 0.038
219
PHR003 Pharyngitis 57 0.038
220
GST050 Gastrointestinal System Disease 56 0.038
221
HYP005 Hypokalemia 55 0.038
222
P MLN007 Male Infertility 55 0.038
223
CHR100 Chronic Ulcer of Skin 55 0.038
224
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.038
225
AMN003 Amnestic Disorder 54 0.038
226
GLC003 Glucose Intolerance 54 0.038
227
P RST001 Restless Legs Syndrome 54 0.038
228
P ALP008 Alopecia 54 0.038
229
GST037 Gastroparesis 54 0.038
230
P INF037 Inflammatory Bowel Disease 54 0.038
231
CLL003 Cellulitis 54 0.038
232
P PTS002 Ptosis 53 0.038
233
GST023 Gastric Ulcer 53 0.038
234
FCT001 Factor Viii Deficiency 51 0.038
235
c HNT004 Huntington Disease-Like 2 50 0.038
236
c HRD202 Hereditary Lymphedema I 50 0.038
237
P SCK005 Sickle Cell Disease 50 0.038
238
NTR046 Neutrophil Migration 50 0.038
239
ILT001 Ileitis 50 0.038
240
SNT005 Sinoatrial Node Disease 49 0.038
241
ASP007 Aspiration Pneumonia 48 0.038
242
RGH001 Right Bundle Branch Block 48 0.038
243
IGG001 Iga Glomerulonephritis 48 0.038
244
ART004 Aortic Atherosclerosis 47 0.038
245
DRY001 Dry Eye Syndrome 47 0.038
246
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.038
247
BCK003 Background Diabetic Retinopathy 46 0.038
248
GNR003 Generalized Atherosclerosis 46 0.038
249
ADR040 Adrenal Gland Pheochromocytoma 46 0.038
250
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 46 0.038
251
ACT003 Acute Kidney Tubular Necrosis 45 0.038
252
THR099 Third-Degree Atrioventricular Block 45 0.038
253
ASP026 Asplenia, Isolated Congenital 44 0.038
254
RTR001 Retrograde Amnesia 44 0.038
255
RTN021 Retinal Vascular Occlusion 44 0.038
256
CRS005 Crest Syndrome 43 0.038
257
DYS032 Dystrophinopathies 43 0.038
258
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.038
259
CRN020 Coronary Restenosis 39 0.038
260
c HNT011 Huntington Disease-Like 3 38 0.038
261
LVD003 Livedoid Vasculitis 36 0.038
262
CHR178 Chromosomal Triplication 35 0.038
263
PLT015 Platelet Aggregation, Spontaneous 34 0.038
264
c MYC058 Myocardial Infarction 2 34 0.038
265
DXR001 Doxorubicin Induced Cardiomyopathy 33 0.038
266
CYT018 Cytochrome P450 2d6 Variant 27 0.038
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