Search results for Cilostazol

260 hits were found for Cilostazol

# Family MCID Name MIFTS Score
1
INT002 Intermittent Claudication 60 0.488
2
PRP027 Peripheral Vascular Disease 72 0.403
3
ISC004 Ischemia 62 0.377
4
ART140 Arteries, Anomalies of 60 0.321
5
CRB039 Cerebrovascular Disease 71 0.319
6
STR067 Stroke, Ischemic 82 0.314
7
PRP080 Peripheral Artery Disease 51 0.301
8
P VSC007 Vascular Disease 65 0.294
9
P CRN018 Coronary Artery Anomaly 67 0.252
10
ATH013 Atherosclerosis Susceptibility 68 0.234
11
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.213
12
P MYC007 Myocardial Infarction 74 0.210
13
P CRN300 Coronary Heart Disease 1 59 0.210
14
P HDC001 Headache 59 0.191
15
P ART021 Arteriosclerosis 56 0.191
16
LMB062 Limb Ischemia 50 0.191
17
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.187
18
THR024 Thrombosis 58 0.174
19
P DMN002 Dementia 68 0.170
20
c MGR028 Migraine with or Without Aura 1 70 0.165
21
P DBT009 Diabetes Mellitus 66 0.165
22
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.165
23
c ACT075 Acute Myocardial Infarction 59 0.165
24
P ALZ034 Alzheimer Disease 90 0.151
25
ANG054 Angina Pectoris 66 0.151
26
P TRN020 Turner Syndrome 66 0.151
27
KHL003 Kohlschutter-Tonz Syndrome 63 0.151
28
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 36 0.151
29
c MCR113 Microvascular Complications of Diabetes 3 55 0.146
30
c MCR120 Microvascular Complications of Diabetes 7 48 0.146
31
c MCR130 Microvascular Complications of Diabetes 6 42 0.146
32
c MCR133 Microvascular Complications of Diabetes 4 42 0.146
33
ART008 Arteriosclerosis Obliterans 40 0.146
34
P KDN018 Kidney Disease 73 0.140
35
LPD008 Lipid Metabolism Disorder 64 0.140
36
P HRT032 Heart Disease 78 0.135
37
P MCR115 Microvascular Complications of Diabetes 5 67 0.135
38
ADL002 Adult Syndrome 62 0.135
39
CRT013 Carotid Stenosis 50 0.135
40
CLP006 Clopidogrel Resistance 41 0.135
41
CRB004 Cerebral Artery Occlusion 38 0.135
42
P NRP001 Neuropathy 57 0.129
43
P EXN002 Exanthem 58 0.123
44
CRN030 Coronary Stenosis 49 0.123
45
c HYP595 Hypertension, Essential 87 0.117
46
P BLD124 Bleeding Disorder, Platelet-Type, 11 66 0.117
47
TRN015 Transient Cerebral Ischemia 62 0.117
48
VSC002 Vascular Dementia 57 0.117
49
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.117
50
P MGR001 Migraine Without Aura 47 0.117
51
48X005 48,xyyy 37 0.117
52
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.110
53
HYP066 Hyperglycemia 63 0.110
54
DBT010 Diabetic Neuropathy 56 0.110
55
P DRR001 Diarrhea 55 0.110
56
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.110
57
GSG001 Gas Gangrene 52 0.110
58
CYT002 Cytokine Deficiency 46 0.110
59
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.103
60
c HYP836 Hypercholesterolemia, Familial, 1 74 0.103
61
P BRG001 Brugada Syndrome 70 0.103
62
c CHR684 Chronic Kidney Disease 68 0.103
63
HMR039 Hemorrhage, Intracerebral 59 0.103
64
CRT015 Carotid Artery Occlusion 44 0.103
65
c MCR129 Microvascular Complications of Diabetes 1 67 0.095
66
DPR016 Depression 64 0.095
67
P SCK002 Sick Sinus Syndrome 56 0.095
68
CRT016 Carotid Artery Disease 53 0.095
69
BRN071 Brain Injury 51 0.095
70
CRB008 Cerebral Atherosclerosis 47 0.095
71
ASP030 Aspirin Resistance 42 0.095
72
c MCR112 Microvascular Complications of Diabetes 2 42 0.095
73
INT074 Intracranial Arteriosclerosis 17 0.095
74
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.087
75
DWN001 Down Syndrome 70 0.087
76
CNG034 Congestive Heart Failure 69 0.087
77
ANR040 Aneurysm 60 0.087
78
MNT002 Mental Depression 60 0.087
79
END030 End Stage Renal Failure 60 0.087
80
BRG013 Buerger Disease 58 0.087
81
INT007 Intermediate Coronary Syndrome 58 0.087
82
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.087
83
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.087
84
RYN005 Raynaud Phenomenon 50 0.087
85
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.087
86
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.087
87
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.087
88
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.087
89
INT010 Intracranial Embolism 47 0.087
90
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.087
91
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.087
92
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.087
93
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.087
94
CRN017 Coronary Thrombosis 45 0.087
95
P PNM007 Pneumonia 71 0.078
96
P THR014 Thrombocytopenia 67 0.078
97
P NTR004 Neutropenia 64 0.078
98
c PNS012 Paine Syndrome 61 0.078
99
P CRD132 Cardiac Conduction Defect 61 0.078
100
HYP266 Hypoxia 58 0.078
101
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.078
102
ATR057 Atrioventricular Block 56 0.078
103
P PLY019 Polyneuropathy 55 0.078
104
ACT058 Active Peptic Ulcer Disease 55 0.078
105
DBT004 Diabetic Polyneuropathy 48 0.078
106
CRB086 Cerebral Aneurysms 41 0.078
107
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.078
108
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.078
109
c SYS001 Systemic Lupus Erythematosus 88 0.067
110
ANX010 Anxiety 75 0.067
111
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.067
112
HMN044 Human Immunodeficiency Virus Type 1 73 0.067
113
P SYS005 Systemic Scleroderma 68 0.067
114
CNN005 Connective Tissue Disease 68 0.067
115
P NRB010 Neuroblastoma 1 66 0.067
116
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.067
117
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.067
118
ALL026 Allergic Hypersensitivity Disease 65 0.067
119
P PRP019 Peripheral Nervous System Disease 64 0.067
120
c RHB024 Rhabdomyosarcoma 2 64 0.067
121
FTT001 Fatty Liver Disease 63 0.067
122
P LPS004 Lupus Erythematosus 62 0.067
123
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.067
124
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.067
125
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.067
126
ACQ007 Acquired Immunodeficiency Syndrome 61 0.067
127
INT030 Intracranial Aneurysm 57 0.067
128
PRP030 Purpura 56 0.067
129
c FML035 Familial Hyperlipidemia 56 0.067
130
P MGR003 Migraine with Aura 53 0.067
131
RTN003 Retinal Ischemia 52 0.067
132
HYP081 Hypolipoproteinemia 51 0.067
133
RTN020 Retinal Vascular Disease 49 0.067
134
47X002 47,xyy 49 0.067
135
INT078 Intracranial Thrombosis 48 0.067
136
RYN001 Raynaud Disease 48 0.067
137
SYN036 Syncope 46 0.067
138
c HYP272 Hypercholesterolemia, Familial, 3 44 0.067
139
TRP009 Triple X Syndrome 42 0.067
140
c CRN133 Coronary Artery Disease, Autosomal Dominant, 1 31 0.067
141
P CLR023 Colorectal Cancer 100 0.055
142
INS024 Insulin-Like Growth Factor I 79 0.055
143
c PLM164 Pulmonary Hypertension, Primary, 1 79 0.055
144
ART016 Aortic Aneurysm 71 0.055
145
APR006 Apert Syndrome 70 0.055
146
P MJR001 Major Depressive Disorder 69 0.055
147
P TMP003 Temporal Arteritis 68 0.055
148
P HYD006 Hydrocephalus 68 0.055
149
P ATR011 Atrial Fibrillation 67 0.055
150
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.055
151
CLT003 Colitis 63 0.055
152
SPN186 Spinal Cord Injury 63 0.055
153
c ART138 Aortic Aneurysm, Familial Abdominal, 1 62 0.055
154
PPT005 Peptic Ulcer Disease 60 0.055
155
P RHN004 Rhinitis 59 0.055
156
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.055
157
P THR005 Thrombotic Thrombocytopenic Purpura 59 0.055
158
SPN027 Spinal Stenosis 58 0.055
159
IRN002 Iron Metabolism Disease 58 0.055
160
P INF037 Inflammatory Bowel Disease 57 0.055
161
CMR002 Coumarin Resistance 56 0.055
162
GRN034 Grange Syndrome 55 0.055
163
c CNG216 Congenital Hydrocephalus 55 0.055
164
HYP060 Hyperinsulinism 55 0.055
165
MXD005 Mixed Connective Tissue Disease 55 0.055
166
P MYM013 Moyamoya Disease 1 53 0.055
167
CYN002 Cyanosis, Transient Neonatal 45 0.055
168
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.055
169
ALL014 Allergic Encephalomyelitis 40 0.055
170
PRP028 Peripheral Vertigo 39 0.055
171
CNT017 Central Nervous System Origin Vertigo 38 0.055
172
VST001 Vestibular Neuronitis 37 0.055
173
NRN002 Neuronitis 37 0.055
174
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.055
175
c VRL004 Viral Labyrinthitis 28 0.055
176
CRC034 Carcinoma Showing Thymus-Like Differentiation 23 0.055
177
ERL052 Early Repolarization Associated with Ventricular Fibrillation 23 0.055
178
CRB087 Cerebral Arteriosclerosis 23 0.055
179
MNS002 Mini Stroke 20 0.055
180
P RHM011 Rheumatoid Arthritis 82 0.039
181
c DLT002 Dilated Cardiomyopathy 81 0.039
182
AST005 Asthma 80 0.039
183
OST012 Osteoarthritis 80 0.039
184
GST019 Gastrointestinal Stromal Tumor 76 0.039
185
c ATR087 Atrial Standstill 1 76 0.039
186
CRH001 Crohn's Disease 75 0.039
187
GLB002 Glioblastoma 74 0.039
188
P HNT016 Huntington Disease 72 0.039
189
P PHC003 Pheochromocytoma 71 0.039
190
P LVR013 Liver Disease 71 0.039
191
MSC157 Muscular Dystrophy, Duchenne Type 70 0.039
192
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.039
193
P MSC005 Muscular Dystrophy 68 0.039
194
c FML001 Familial Atrial Fibrillation 67 0.039
195
P HYP098 Hypereosinophilic Syndrome 67 0.039
196
P ADN016 Adenocarcinoma 65 0.039
197
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.039
198
MDD011 Mood Disorder 62 0.039
199
MCR013 Microphthalmia 62 0.039
200
c PRG042 Progressive Familial Heart Block, Type Ia 62 0.039
201
P HYP750 Hypertriglyceridemia, Familial 62 0.039
202
c SCL052 Scleroderma, Familial Progressive 62 0.039
203
CRD223 Cardiac Arrhythmia 61 0.039
204
CHL068 Cholestasis 61 0.039
205
PRT013 Portal Hypertension 61 0.039
206
P BCL017 B-Cell Lymphoma 61 0.039
208
P PLY014 Polycystic Kidney Disease 61 0.039
209
GLB015 Glioblastoma Multiforme 60 0.039
210
CHL067 Cholecystitis 60 0.039
211
c ACT071 Acute Kidney Failure 60 0.039
212
P MYC008 Myocarditis 60 0.039
213
ALC006 Alcoholic Hepatitis 60 0.039
214
PLM033 Pulmonary Embolism 60 0.039
215
P ALP008 Alopecia 58 0.039
216
P ALC033 Alcohol Use Disorder 58 0.039
217
GST050 Gastrointestinal System Disease 57 0.039
218
P MLN007 Male Infertility 57 0.039
219
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.039
220
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.039
221
PHR003 Pharyngitis 56 0.039
222
AMN003 Amnestic Disorder 55 0.039
223
HYP005 Hypokalemia 55 0.039
224
CRT033 Corticobasal Degeneration 55 0.039
225
GLC003 Glucose Intolerance 55 0.039
226
P LYM025 Lymphedema 54 0.039
227
P RST001 Restless Legs Syndrome 54 0.039
228
P PTS002 Ptosis 53 0.039
229
CHR100 Chronic Ulcer of Skin 53 0.039
230
P SCK005 Sickle Cell Disease 53 0.039
231
GST023 Gastric Ulcer 53 0.039
232
ADR040 Adrenal Gland Pheochromocytoma 51 0.039
233
ILT001 Ileitis 50 0.039
234
IGG001 Iga Glomerulonephritis 50 0.039
235
NTR046 Neutrophil Migration 49 0.039
236
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 48 0.039
237
c HNT004 Huntington Disease-Like 2 48 0.039
238
c PRG043 Progressive Familial Heart Block, Type Ib 48 0.039
239
RGH001 Right Bundle Branch Block 48 0.039
240
ART004 Aortic Atherosclerosis 47 0.039
241
SNT005 Sinoatrial Node Disease 46 0.039
242
ASP007 Aspiration Pneumonia 46 0.039
243
ASP026 Asplenia, Isolated Congenital 45 0.039
244
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 44 0.039
245
P DYS026 Dysfibrinogenemia 42 0.039
246
RTN021 Retinal Vascular Occlusion 42 0.039
247
DYS032 Dystrophinopathies 42 0.039
248
ACT003 Acute Kidney Tubular Necrosis 42 0.039
249
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.039
250
CRN020 Coronary Restenosis 40 0.039
251
CRS005 Crest Syndrome 40 0.039
252
PLT015 Platelet Aggregation, Spontaneous 40 0.039
253
GNR003 Generalized Atherosclerosis 39 0.039
254
THR099 Third-Degree Atrioventricular Block 39 0.039
255
LVD003 Livedoid Vasculitis 39 0.039
256
RTR001 Retrograde Amnesia 38 0.039
257
c HNT011 Huntington Disease-Like 3 37 0.039
258
BCK003 Background Diabetic Retinopathy 37 0.039
259
DXR001 Doxorubicin Induced Cardiomyopathy 34 0.039
260
c MYC058 Myocardial Infarction 2 30 0.039
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