Search results for Cilostazol

373 hits were found for Cilostazol

# Family MCID Name MIFTS Score
1
INT002 Intermittent Claudication 61 25.874
2
PRP027 Peripheral Vascular Disease 71 22.600
3
ART140 Arteries, Anomalies of 53 15.984
4
ISC004 Ischemia 61 15.844
5
PRP080 Peripheral Artery Disease 54 15.716
6
P VSC007 Vascular Disease 63 14.676
7
STR067 Stroke, Ischemic 80 13.646
8
LMB062 Limb Ischemia 55 10.937
9
CRB039 Cerebrovascular Disease 66 10.782
10
P HDC001 Headache 57 10.226
11
c TYP009 Type 2 Diabetes Mellitus 92 9.252
12
LPP008 Lipoprotein Quantitative Trait Locus 65 9.216
13
P MYC007 Myocardial Infarction 70 8.883
14
P ART021 Arteriosclerosis 54 8.294
15
c ACT075 Acute Myocardial Infarction 56 8.258
16
P CRN300 Coronary Heart Disease 1 73 8.245
17
c MGR028 Migraine with or Without Aura 1 64 8.177
18
P HRT032 Heart Disease 81 7.680
19
ATH013 Atherosclerosis Susceptibility 63 7.646
20
c MCR130 Microvascular Complications of Diabetes 6 41 7.407
21
c MCR120 Microvascular Complications of Diabetes 7 47 7.407
22
c MCR113 Microvascular Complications of Diabetes 3 52 7.407
23
c MCR133 Microvascular Complications of Diabetes 4 41 7.407
24
P DBT009 Diabetes Mellitus 67 7.404
25
TRN015 Transient Cerebral Ischemia 63 7.309
26
P DMN002 Dementia 66 7.299
27
LPD008 Lipid Metabolism Disorder 62 7.227
28
CRB004 Cerebral Artery Occlusion 45 7.021
29
c MCR115 Microvascular Complications of Diabetes 5 65 6.831
30
THR024 Thrombosis 56 6.701
31
ART008 Arteriosclerosis Obliterans 40 6.628
32
CLP006 Clopidogrel Resistance 44 6.362
33
c HYP836 Hypercholesterolemia, Familial, 1 73 6.247
34
VSC002 Vascular Dementia 60 6.240
35
ANG054 Angina Pectoris 66 6.227
36
P ALZ034 Alzheimer Disease 87 5.774
37
MLD018 Mild Cognitive Impairment 48 5.612
38
ANR040 Aneurysm 61 5.403
39
DBT010 Diabetic Neuropathy 54 5.375
40
CYT002 Cytokine Deficiency 43 5.373
41
c CHR684 Chronic Kidney Disease 69 5.244
42
CRT013 Carotid Stenosis 51 5.206
43
CRN030 Coronary Stenosis 50 5.150
44
P NRP001 Neuropathy 60 5.066
45
P MGR001 Migraine Without Aura 49 4.962
46
P RHM011 Rheumatoid Arthritis 82 4.929
47
NNL005 Non-Alcoholic Fatty Liver Disease 63 4.848
48
CRB009 Cerebritis 43 4.788
49
P BRG001 Brugada Syndrome 69 4.781
50
CRT015 Carotid Artery Occlusion 45 4.765
51
BRG013 Buerger Disease 57 4.686
52
CNG034 Congestive Heart Failure 69 4.558
53
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 4.520
54
CRB008 Cerebral Atherosclerosis 46 4.512
55
P SCK002 Sick Sinus Syndrome 55 4.477
56
CRN017 Coronary Thrombosis 46 4.365
57
RYN005 Raynaud Phenomenon 45 4.327
58
HYP066 Hyperglycemia 61 4.321
59
P CRD246 Cardiovascular System Disease 56 4.299
60
P KDN018 Kidney Disease 72 4.281
61
BRN071 Brain Injury 50 4.239
62
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 4.193
63
P PNM007 Pneumonia 67 4.068
64
P ART022 Arthritis 71 4.021
65
P DRR001 Diarrhea 55 4.005
66
P MCR129 Microvascular Complications of Diabetes 1 68 4.002
67
c MCR112 Microvascular Complications of Diabetes 2 42 4.002
68
ASP030 Aspirin Resistance 40 3.953
69
P MGR003 Migraine with Aura 52 3.864
70
P EXN002 Exanthem 58 3.750
71
INT030 Intracranial Aneurysm 55 3.738
72
P ATR011 Atrial Fibrillation 66 3.726
73
FTT001 Fatty Liver Disease 62 3.701
74
CRD132 Cardiac Conduction Defect 60 3.657
75
SYN036 Syncope 45 3.633
76
c HYP595 Hypertension, Essential 85 3.595
77
c HYP724 Hyperlipoproteinemia, Type Iii 67 3.560
78
AGN016 Aging 54 3.534
79
c BLD140 Blood Group, I System 46 3.502
80
CRB086 Cerebral Aneurysms 40 3.469
81
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 3.461
82
RTN003 Retinal Ischemia 49 3.461
83
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 3.410
84
DWN001 Down Syndrome 70 3.338
85
END072 Endotheliitis 36 3.338
86
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 63 3.338
87
P PLY019 Polyneuropathy 52 3.335
88
RTN020 Retinal Vascular Disease 46 3.305
89
ATR057 Atrioventricular Block 54 3.295
90
INT007 Intermediate Coronary Syndrome 54 3.251
91
P PRP019 Peripheral Nervous System Disease 58 3.138
92
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 3.131
93
ART016 Aortic Aneurysm 68 3.131
94
ASP026 Asplenia, Isolated Congenital 43 3.111
95
GSG001 Gas Gangrene 52 3.104
97
P RHN004 Rhinitis 57 3.022
98
PRT251 Proteinuria, Chronic Benign 57 3.020
99
CLT003 Colitis 63 2.958
100
PRP030 Purpura 54 2.958
101
P MJR001 Major Depressive Disorder 68 2.942
102
MNT002 Mental Depression 57 2.942
103
DPR016 Depression 65 2.942
104
48X005 48,xyyy 39 2.894
105
P TRN020 Turner Syndrome 67 2.869
106
P SYS005 Systemic Scleroderma 74 2.857
107
SPN186 Spinal Cord Injury 61 2.846
108
CRC034 Carcinoma Showing Thymus-Like Differentiation 22 2.846
109
P NRB001 Neuroblastoma 66 2.784
110
P HYD006 Hydrocephalus 61 2.784
111
SPN027 Spinal Stenosis 59 2.784
112
ALL014 Allergic Encephalomyelitis 34 2.720
113
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 2.680
114
KHL003 Kohlschutter-Tonz Syndrome 59 2.673
115
PHR003 Pharyngitis 58 2.620
116
P THR014 Thrombocytopenia 66 2.614
117
P MYM013 Moyamoya Disease 1 59 2.586
118
HYP060 Hyperinsulinism 54 2.586
119
P LVR013 Liver Disease 69 2.558
120
INS024 Insulin-Like Growth Factor I 78 2.515
121
P NTR004 Neutropenia 63 2.455
122
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.441
123
ACT058 Active Peptic Ulcer Disease 56 2.440
124
HYP266 Hypoxia 57 2.440
125
P BLD124 Bleeding Disorder, Platelet-Type, 11 67 2.419
126
c PLM164 Pulmonary Hypertension, Primary, 1 76 2.363
127
P PHC003 Pheochromocytoma 69 2.359
128
ADR040 Adrenal Gland Pheochromocytoma 46 2.359
129
CRN020 Coronary Restenosis 39 2.359
130
ADL002 Adult Syndrome 70 2.306
131
c TYP008 Type 1 Diabetes Mellitus 70 2.288
132
ASP007 Aspiration Pneumonia 49 2.288
133
P THR005 Thrombotic Thrombocytopenic Purpura 64 2.281
134
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 54 2.259
135
c SYS001 Systemic Lupus Erythematosus 87 2.238
136
P LPS004 Lupus Erythematosus 61 2.238
137
PLM033 Pulmonary Embolism 58 2.214
138
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 2.195
139
CYN002 Cyanosis, Transient Neonatal 43 2.195
140
HMR039 Hemorrhage, Intracerebral 57 2.146
141
P ANR048 Aniridia 1 64 2.146
142
ANT039 Antisynthetase Syndrome 55 2.146
143
GLC003 Glucose Intolerance 54 2.137
144
OST012 Osteoarthritis 77 2.137
145
ALC006 Alcoholic Hepatitis 61 2.137
146
BCK003 Background Diabetic Retinopathy 47 2.137
147
P MYC008 Myocarditis 59 2.137
148
INT078 Intracranial Thrombosis 50 2.070
149
c MYC058 Myocardial Infarction 2 24 2.055
150
IGG001 Iga Glomerulonephritis 50 2.055
151
PRT013 Portal Hypertension 59 2.055
152
MCR013 Microphthalmia 60 2.055
153
CHL068 Cholestasis 61 2.055
154
INT074 Intracranial Arteriosclerosis 22 2.018
155
INT010 Intracranial Embolism 48 2.004
156
CRD223 Cardiac Arrhythmia 63 1.969
157
P HNT016 Huntington Disease 73 1.969
158
P ALP008 Alopecia 54 1.969
159
47X002 47,xyy 48 1.969
160
GNR003 Generalized Atherosclerosis 43 1.969
161
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 1.962
162
ERL052 Early Repolarization Associated with Ventricular Fibrillation 22 1.897
163
c SCL052 Scleroderma, Familial Progressive 61 1.877
164
CHR100 Chronic Ulcer of Skin 57 1.877
165
THR099 Third-Degree Atrioventricular Block 42 1.877
166
P RST001 Restless Legs Syndrome 52 1.877
167
PLT015 Platelet Aggregation, Spontaneous 34 1.877
168
P ALC033 Alcohol Use Disorder 61 1.877
169
CNN005 Connective Tissue Disease 67 1.877
170
RTR001 Retrograde Amnesia 41 1.877
171
c ACT027 Acute Pancreatitis 60 1.877
172
P PTS002 Ptosis 52 1.877
173
GST037 Gastroparesis 52 1.877
174
AMN003 Amnestic Disorder 54 1.877
175
DBT004 Diabetic Polyneuropathy 50 1.877
176
RHB024 Rhabdomyosarcoma 2 67 1.866
177
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 1.809
178
P SCH015 Schizophrenia 74 1.778
179
MSC157 Muscular Dystrophy, Duchenne Type 79 1.778
180
P PLY014 Polycystic Kidney Disease 69 1.778
181
RHM028 Rheumatic Heart Disease 56 1.778
182
P BCL017 B-Cell Lymphoma 59 1.778
183
P MSC005 Muscular Dystrophy 67 1.778
184
HYP005 Hypokalemia 55 1.778
185
P MLN007 Male Infertility 56 1.778
186
P PNC044 Pancreatitis 61 1.778
187
P INF032 Infertility 57 1.778
188
DYS032 Dystrophinopathies 47 1.778
189
RYN001 Raynaud Disease 50 1.692
190
c PRG042 Progressive Familial Heart Block, Type Ia 66 1.671
191
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.671
192
GST019 Gastrointestinal Stromal Tumor 78 1.671
193
ACT003 Acute Kidney Tubular Necrosis 46 1.671
194
SVR001 Severe Acute Respiratory Syndrome 67 1.671
195
CLL003 Cellulitis 53 1.671
196
ART004 Aortic Atherosclerosis 47 1.671
197
c VRL005 Viral Pneumonia 53 1.671
198
P THR015 Thrombophilia 51 1.671
199
GST023 Gastric Ulcer 52 1.671
200
RTN021 Retinal Vascular Occlusion 45 1.671
201
CHR178 Chromosomal Triplication 34 1.671
202
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 1.670
203
P SPR120 Supranuclear Palsy, Progressive, 1 69 1.552
204
ILT001 Ileitis 48 1.552
205
CRS005 Crest Syndrome 36 1.552
206
c PRG043 Progressive Familial Heart Block, Type Ib 54 1.552
207
RPD005 Rapidly Involuting Congenital Hemangioma 46 1.552
208
CRH001 Crohn's Disease 80 1.552
209
DRY001 Dry Eye Syndrome 50 1.552
210
GT001 Gout 64 1.552
211
ALL029 Allergic Disease 59 1.552
212
RGH001 Right Bundle Branch Block 47 1.552
213
CRB087 Cerebral Arteriosclerosis 17 1.484
214
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 1.459
215
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.459
216
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.459
217
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.459
218
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 1.459
219
P INT260 Intracranial Berry Aneurysm 40 1.459
220
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 1.459
221
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 1.459
222
c HYP272 Hypercholesterolemia, Familial, 3 45 1.459
223
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 1.459
224
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.459
225
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 1.459
226
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.459
227
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 1.459
228
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 1.459
229
END040 Endogenous Depression 55 1.459
230
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 1.459
231
NRT001 Neurotic Disorder 56 1.459
232
CRT016 Carotid Artery Disease 52 1.459
233
FML035 Familial Hyperlipidemia 55 1.459
234
AND005 Androgen Insensitivity Syndrome, Mild 21 1.459
235
c PRM038 Primary Agammaglobulinemia 47 1.459
236
HMC014 Homocysteinemia 52 1.423
237
P AMY004 Amyloidosis 70 1.423
238
END086 End Stage Renal Disease 52 1.423
239
CNS004 Constipation 56 1.423
240
P HYP086 Hypothyroidism 69 1.423
241
MDD011 Mood Disorder 62 1.417
242
CRT033 Corticobasal Degeneration 47 1.417
243
P HYP098 Hypereosinophilic Syndrome 66 1.257
244
CHL067 Cholecystitis 60 1.257
245
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.257
246
IMP005 Impotence 52 1.232
247
BRN004 Brain Edema 54 1.125
248
VSC004 Vasculogenic Impotence 29 1.125
249
P CMP008 Compartment Syndrome 50 1.125
250
c ATR087 Atrial Standstill 1 74 1.049
251
P INF037 Inflammatory Bowel Disease 53 1.049
252
P STR092 Striatal Degeneration, Autosomal Dominant 2 47 1.049
253
INT323 Intraocular Pressure Quantitative Trait Locus 64 1.049
254
c DLT002 Dilated Cardiomyopathy 78 1.049
255
GST050 Gastrointestinal System Disease 55 1.049
256
P SCK005 Sickle Cell Disease 56 1.049
257
DXR001 Doxorubicin Induced Cardiomyopathy 32 1.049
258
HRW001 Hair Whorl 35 1.006
259
ALL006 Allergic Asthma 56 1.006
260
P ESS003 Essential Thrombocythemia 69 1.006
261
MYL031 Myeloproliferative Neoplasm 66 1.006
262
MXD005 Mixed Connective Tissue Disease 57 0.980
263
VST001 Vestibular Neuronitis 33 0.954
264
P PRS038 Personality Disorder 65 0.954
265
VRL004 Viral Labyrinthitis 34 0.954
266
NRN002 Neuronitis 31 0.954
267
ATM095 Autoimmune Disease 61 0.871
268
c SPN225 Spondyloarthropathy 1 70 0.871
269
c LKM061 Leukemia, Acute Myeloid 83 0.871
270
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 0.871
271
MYL069 Myeloma, Multiple 77 0.871
272
PRT037 Pertussis 65 0.871
273
SWL001 Swallowing Disorders 38 0.871
274
SPN051 Spondylitis 51 0.871
275
INF009 Inflammatory Spondylopathy 30 0.871
276
CHL014 Cholera 62 0.871
277
ASC004 Ascending Colon Cancer 42 0.871
278
THR004 Thrombocytosis 53 0.871
279
TBL003 Tubular Adenocarcinoma 40 0.871
280
P TCD001 Tic Disorder 49 0.871
281
SPS057 Spasticity 42 0.711
282
P BRS047 Breast Cancer 98 0.711
283
FCT001 Factor Viii Deficiency 60 0.711
284
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 0.711
285
c HMP029 Hemophilia a 68 0.711
286
ATR089 Atrioventricular Dissociation 21 0.711
287
CRD137 Cardiogenic Shock 56 0.711
288
P VSC011 Vasculitis 61 0.711
289
SYS071 Systemic Autoimmune Disease 35 0.711
290
P ANT006 Antiphospholipid Syndrome 55 0.711
291
NRM005 Neuromuscular Disease 63 0.711
292
PLM180 Pulmonary Artery Disease 34 0.711
293
SPN020 Spondylosis 46 0.711
294
ALC009 Alcoholic Liver Cirrhosis 54 0.711
295
P ANG015 Angioedema 56 0.711
296
LVR012 Liver Cirrhosis 63 0.711
297
CRT004 Carotid Artery Thrombosis 39 0.711
298
PTN001 Patent Foramen Ovale 62 0.711
299
CHR073 Choreatic Disease 54 0.711
300
c ACQ014 Acquired Hemophilia 45 0.711
301
c ACQ042 Acquired Hemophilia a 37 0.711
302
P HMP007 Hemophilia 52 0.711
303
LVD003 Livedoid Vasculitis 35 0.546
304
SNT005 Sinoatrial Node Disease 47 0.546
305
c ACT071 Acute Kidney Failure 60 0.546
306
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 46 0.546
307
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 45 0.546
308
DFF031 Diffuse Alveolar Hemorrhage 31 0.503
309
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 0.503
310
STN005 St Anthony's Fire 18 0.503
311
THR123 Thrombotic Microangiopathy 40 0.503
312
FRN006 Frontotemporal Dementia 68 0.503
313
ALL003 Allergic Rhinitis 67 0.503
314
P DRM053 Dermatitis, Atopic 65 0.503
315
GST092 Gastroesophageal Reflux 61 0.503
316
c LKM063 Leukemia, Chronic Myeloid 71 0.503
317
P PLM037 Pulmonary Hypertension 72 0.503
318
P ACR001 Aicardi-Goutieres Syndrome 63 0.503
319
MLT073 Multisystemic Smooth Muscle Dysfunction Syndrome 44 0.503
320
APH002 Aphasia 56 0.503
321
APR001 Apraxia 52 0.503
322
P LYM033 Lymphoproliferative Syndrome 59 0.503
323
HLC007 Helicobacter Pylori Infection 67 0.503
324
c LNG048 Long Qt Syndrome 3 53 0.503
325
c LNG047 Long Qt Syndrome 2 59 0.503
326
P GST053 Gastric Cancer 83 0.503
327
HRN029 Hearing Loss, Noise-Induced 37 0.503
328
MYL005 Myelofibrosis 71 0.503
329
DSS032 Disease by Infectious Agent 55 0.503
331
P HMC002 Homocystinuria 53 0.503
332
P HML002 Hemolytic Anemia 62 0.503
333
P TRM003 Tremor 48 0.503
334
P PLM034 Pulmonary Emphysema 58 0.503
335
c FML191 Familial Long Qt Syndrome 55 0.503
336
PNC129 Pancreatic Adenocarcinoma 65 0.503
337
CRB031 Cerebral Arterial Disease 33 0.503
338
P PLM036 Pulmonary Fibrosis 66 0.503
339
THR016 Thrombophlebitis 50 0.503
340
PPT005 Peptic Ulcer Disease 58 0.503
341
RDC002 Radiculopathy 52 0.503
342
MCR011 Microinvasive Gastric Cancer 41 0.503
343
P GRF003 Graft-Versus-Host Disease 71 0.503
344
LFT001 Left Bundle Branch Hemiblock 47 0.503
345
TNS005 Tonsillitis 57 0.503
346
CMM004 Common Variable Immunodeficiency 72 0.503
347
DYS009 Dysthymic Disorder 52 0.503
348
P LKM002 Leukemia 67 0.503
349
P AGM001 Agammaglobulinemia 68 0.503
350
ACL001 Acalculous Cholecystitis 38 0.503
351
P LNG028 Long Qt Syndrome 64 0.503
352
DBT008 Diabetic Angiopathy 45 0.503
353
P CRD119 Cardiac Arrest 67 0.503
354
c INF023 Inflammatory Breast Carcinoma 49 0.503
355
LTR003 Lateral Medullary Syndrome 36 0.503
356
MRP001 Morphine Dependence 42 0.503
357
P LRY019 Laryngitis 53 0.503
358
RNL097 Renal Artery Disease 40 0.503
359
P RTN022 Retinal Vein Occlusion 54 0.503
360
HPR003 Heparin-Induced Thrombocytopenia 47 0.503
361
HDN002 Head Injury 44 0.503
362
P CHR345 Chronic Pain 50 0.503
363
PTT037 Pituitary Tumors 44 0.503
364
BCK006 Back Pain 47 0.503
365
DYS073 Dysphagia 53 0.503
366
ATH004 Athetosis 25 0.503
367
c CHR417 Chronic Graft Versus Host Disease 55 0.503
368
CHR682 Chronic Bilirubin Encephalopathy 37 0.476
369
c FML001 Familial Atrial Fibrillation 65 0.476
370
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 70 0.476
371
CTS005 Catastrophic Antiphospholipid Syndrome 43 0.476
372
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.476
373
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.476
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