Search results for Clopidogrel

573 hits were found for Clopidogrel

# Family MCID Name MIFTS Score
1
CLP006 Clopidogrel Resistance 40 5.833
3
ISC004 Ischemia 58 1.036
4
LPP008 Lipoprotein Quantitative Trait Locus 62 0.835
5
ART140 Arteries, Anomalies of 52 0.733
6
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.724
7
P CRN300 Coronary Heart Disease 1 63 0.649
8
P MYC007 Myocardial Infarction 70 0.615
9
THR024 Thrombosis 57 0.534
10
CRB039 Cerebrovascular Disease 67 0.520
11
STR067 Stroke, Ischemic 81 0.510
12
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.458
13
INT007 Intermediate Coronary Syndrome 55 0.419
14
c ACT075 Acute Myocardial Infarction 57 0.372
15
TRN015 Transient Cerebral Ischemia 63 0.368
16
P VSC007 Vascular Disease 63 0.357
17
ANG054 Angina Pectoris 66 0.356
18
PRP027 Peripheral Vascular Disease 71 0.355
19
P HRT032 Heart Disease 75 0.317
20
PRP080 Peripheral Artery Disease 53 0.272
21
P CRD246 Cardiovascular System Disease 57 0.270
22
ATH013 Atherosclerosis Susceptibility 65 0.262
23
P KDN018 Kidney Disease 72 0.261
24
P ATR011 Atrial Fibrillation 66 0.259
25
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.253
26
c CHR684 Chronic Kidney Disease 70 0.239
27
ASP030 Aspirin Resistance 39 0.230
28
PRP030 Purpura 54 0.211
29
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.209
30
P DBT009 Diabetes Mellitus 64 0.192
31
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.192
32
c FML001 Familial Atrial Fibrillation 65 0.190
33
P EXN002 Exanthem 57 0.190
34
P THR014 Thrombocytopenia 67 0.188
35
ALL026 Allergic Hypersensitivity Disease 62 0.188
36
ACT058 Active Peptic Ulcer Disease 55 0.188
37
48X005 48,xyyy 39 0.188
38
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.186
39
ANR040 Aneurysm 59 0.186
40
PPT005 Peptic Ulcer Disease 59 0.186
41
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.183
42
CYT018 Cytochrome P450 2d6 Variant 27 0.181
43
P TRN020 Turner Syndrome 67 0.179
44
P NTR004 Neutropenia 63 0.176
45
CRT013 Carotid Stenosis 50 0.176
46
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.174
47
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.169
48
c RHB024 Rhabdomyosarcoma 2 67 0.164
49
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.164
50
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.161
51
CNG034 Congestive Heart Failure 69 0.156
52
GSG001 Gas Gangrene 53 0.156
53
LMB062 Limb Ischemia 55 0.153
54
c HYP595 Hypertension, Essential 84 0.148
55
DWN001 Down Syndrome 70 0.136
56
P ART021 Arteriosclerosis 54 0.136
57
CRD137 Cardiogenic Shock 47 0.136
58
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.133
59
P CRD119 Cardiac Arrest 67 0.130
60
INT002 Intermittent Claudication 61 0.130
61
END086 End Stage Renal Disease 51 0.130
62
CRN030 Coronary Stenosis 50 0.130
63
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.130
64
c HYP836 Hypercholesterolemia, Familial, 1 73 0.126
65
LPD008 Lipid Metabolism Disorder 62 0.126
66
GST023 Gastric Ulcer 53 0.126
67
CRB086 Cerebral Aneurysms 40 0.126
68
c THR092 Thrombophilia Due to Thrombin Defect 73 0.123
69
INT030 Intracranial Aneurysm 56 0.119
70
VTM033 Vitamin K Deficiency Bleeding 48 0.119
71
CRN017 Coronary Thrombosis 47 0.119
72
ATX019 Ataxia with Vitamin E Deficiency 42 0.119
73
P ART022 Arthritis 69 0.108
74
CMR002 Coumarin Resistance 56 0.104
75
P DRR001 Diarrhea 55 0.104
76
DFC004 Deficiency Anemia 70 0.100
77
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.100
78
P HDC001 Headache 57 0.100
79
BLD053 Blood Platelet Disease 49 0.100
80
ADL002 Adult Syndrome 70 0.096
81
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.096
82
P CRN133 Coronary Artery Disease, Autosomal Dominant, 1 32 0.096
83
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 19 0.096
84
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.092
85
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.092
86
P LVR013 Liver Disease 68 0.092
87
c MGR028 Migraine with or Without Aura 1 67 0.092
88
c ART101 Aortic Valve Disease 2 65 0.092
89
P ESP024 Esophagitis 62 0.092
90
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.092
91
PPT001 Peptic Esophagitis 52 0.092
92
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.092
93
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.092
94
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.092
95
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.092
96
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.092
97
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.092
98
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.092
99
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.092
100
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.092
101
P RSP003 Respiratory Failure 74 0.087
102
PLM033 Pulmonary Embolism 59 0.087
103
P HMR003 Hemorrhagic Disease 53 0.087
104
c HYP272 Hypercholesterolemia, Familial, 3 44 0.087
105
c ART115 Aortic Valve Disease 1 75 0.082
106
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.082
107
NTR005 Nutritional Deficiency Disease 62 0.082
108
LNG099 Lung Disease 60 0.082
109
HMR039 Hemorrhage, Intracerebral 57 0.082
110
P ANG015 Angioedema 57 0.082
111
P DDN001 Duodenal Ulcer 52 0.082
112
OCL069 Ocular Motor Apraxia 51 0.082
113
P THR015 Thrombophilia 51 0.082
114
HPR006 Heparin Cofactor Ii Deficiency 40 0.082
115
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.082
116
P OCL013 Oculodentodigital Dysplasia 69 0.077
117
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.077
118
P GST044 Gastritis 56 0.077
119
ZLL002 Zollinger-Ellison Syndrome 55 0.077
120
P HML001 Hemolytic-Uremic Syndrome 53 0.077
121
CRT016 Carotid Artery Disease 52 0.077
122
P CLR023 Colorectal Cancer 99 0.071
123
LPT014 Leptin Deficiency or Dysfunction 74 0.071
124
APR006 Apert Syndrome 70 0.071
125
P PNM007 Pneumonia 68 0.071
126
P MCR115 Microvascular Complications of Diabetes 5 66 0.071
127
HYP056 Hypoglycemia 66 0.071
128
P HML002 Hemolytic Anemia 63 0.071
129
P ATR010 Atrial Heart Septal Defect 60 0.071
130
HLC007 Helicobacter Pylori Infection 59 0.071
131
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.071
132
c MCR113 Microvascular Complications of Diabetes 3 52 0.071
133
47X002 47,xyy 49 0.071
134
c MCR120 Microvascular Complications of Diabetes 7 47 0.071
135
MDS022 Mediastinitis 46 0.071
136
c MCR130 Microvascular Complications of Diabetes 6 41 0.071
137
c MCR133 Microvascular Complications of Diabetes 4 41 0.071
138
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.065
139
P APL001 Aplastic Anemia 74 0.065
140
ART016 Aortic Aneurysm 69 0.065
141
GST092 Gastroesophageal Reflux 67 0.065
142
P DMN002 Dementia 66 0.065
143
KHL003 Kohlschutter-Tonz Syndrome 65 0.065
144
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.065
145
ATM095 Autoimmune Disease 62 0.065
146
P LPS004 Lupus Erythematosus 61 0.065
147
c ACT071 Acute Kidney Failure 60 0.065
148
CNS004 Constipation 58 0.065
149
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.065
150
HYP266 Hypoxia 57 0.065
151
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.065
152
HRT012 Heart Valve Disease 53 0.065
153
PRP016 Paraplegia 52 0.065
154
THR004 Thrombocytosis 51 0.065
156
BHR001 Behr Syndrome 51 0.065
157
RTN003 Retinal Ischemia 50 0.065
158
HDN002 Head Injury 46 0.065
159
ASP026 Asplenia, Isolated Congenital 44 0.065
160
BCK006 Back Pain 42 0.065
161
P CRN074 Coronary Artery Aneurysm 39 0.065
162
CRN006 Coronary Aneurysm 39 0.065
163
PPT002 Peptic Ulcer Perforation 36 0.065
164
c SYS001 Systemic Lupus Erythematosus 86 0.058
165
P GST053 Gastric Cancer 83 0.058
166
HMN044 Human Immunodeficiency Virus Type 1 71 0.058
167
MYL009 Myelodysplastic Syndrome 70 0.058
168
c DBT099 Diabetes Mellitus, Type I 65 0.058
169
P VSC011 Vasculitis 62 0.058
170
LVR012 Liver Cirrhosis 62 0.058
171
HYP066 Hyperglycemia 61 0.058
172
P PNC044 Pancreatitis 61 0.058
173
PTN001 Patent Foramen Ovale 60 0.058
174
ADN018 Adenoma 59 0.058
175
CRD132 Cardiac Conduction Defect 58 0.058
176
P NRP001 Neuropathy 56 0.058
177
AGN016 Aging 56 0.058
178
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.058
179
c FML035 Familial Hyperlipidemia 55 0.058
180
c PRG126 Progressive Familial Heart Block 55 0.058
181
ACR041 Acromelic Frontonasal Dysostosis 52 0.058
182
P HMP007 Hemophilia 51 0.058
183
FCT001 Factor Viii Deficiency 51 0.058
184
HYP081 Hypolipoproteinemia 51 0.058
185
HRT011 Heart Septal Defect 50 0.058
186
INT010 Intracranial Embolism 48 0.058
187
c ACQ014 Acquired Hemophilia 45 0.058
188
GRN017 Granulocytopenia 44 0.058
189
CRB008 Cerebral Atherosclerosis 44 0.058
190
PPL001 Papillary Adenoma 44 0.058
191
c PRM038 Primary Agammaglobulinemia 44 0.058
192
CVD001 Covid-19 44 0.058
193
MCR011 Microinvasive Gastric Cancer 43 0.058
194
TRP009 Triple X Syndrome 42 0.058
195
ANG049 Angioedema Induced by Ace Inhibitors 40 0.058
196
CRT004 Carotid Artery Thrombosis 38 0.058
197
HRT040 Hirata Disease 38 0.058
198
DDN009 Duodenal Obstruction 34 0.058
199
c MYC058 Myocardial Infarction 2 34 0.058
200
P ALZ034 Alzheimer Disease 88 0.050
201
P PNC035 Pancreatic Cancer 84 0.050
202
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.050
203
AST005 Asthma 76 0.050
204
c ATR087 Atrial Standstill 1 75 0.050
205
ANX010 Anxiety 73 0.050
206
P MJR001 Major Depressive Disorder 68 0.050
207
PNC129 Pancreatic Adenocarcinoma 68 0.050
208
P PLM037 Pulmonary Hypertension 67 0.050
209
c MCR129 Microvascular Complications of Diabetes 1 66 0.050
210
P ADN016 Adenocarcinoma 64 0.050
211
DPR016 Depression 63 0.050
212
c FNC043 Fanconi Anemia, Complementation Group E 62 0.050
213
c SVR001 Severe Acute Respiratory Syndrome 62 0.050
214
c ACT027 Acute Pancreatitis 60 0.050
215
CRD223 Cardiac Arrhythmia 60 0.050
216
ACQ007 Acquired Immunodeficiency Syndrome 60 0.050
217
SQM006 Squamous Cell Carcinoma 60 0.050
218
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.050
219
PRT058 Pure Autonomic Failure 59 0.050
220
P URT039 Urticaria 58 0.050
221
MNT002 Mental Depression 58 0.050
222
P INF032 Infertility 57 0.050
223
APH002 Aphasia 57 0.050
224
c ACT134 Acute Liver Failure 56 0.050
225
P HYP838 Hyperlipidemia, Familial Combined, 3 56 0.050
226
HYP005 Hypokalemia 55 0.050
227
CNN011 Cenani-Lenz Syndactyly Syndrome 55 0.050
228
P SBS003 Substance Abuse 55 0.050
229
END040 Endogenous Depression 55 0.050
230
PLM010 Pulmonary Edema 54 0.050
231
PNC001 Pancytopenia 54 0.050
232
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.050
233
P TCD001 Tic Disorder 53 0.050
234
NRT001 Neurotic Disorder 53 0.050
235
c HYP740 Hyperlipoproteinemia, Type V 53 0.050
236
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.050
237
HYP014 Hyperuricemia 52 0.050
238
P MGR003 Migraine with Aura 52 0.050
239
PNG002 Pain Agnosia 51 0.050
240
P MND003 Mandibuloacral Dysplasia with Type a Lipodystrophy 51 0.050
241
TRM010 Traumatic Brain Injury 51 0.050
242
RDC002 Radiculopathy 50 0.050
243
PLC008 Placenta Disease 50 0.050
244
P LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 50 0.050
245
SYS003 Systolic Heart Failure 49 0.050
246
LFT001 Left Bundle Branch Hemiblock 49 0.050
247
BRN071 Brain Injury 49 0.050
248
HPR003 Heparin-Induced Thrombocytopenia 48 0.050
249
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 47 0.050
250
CRD001 Cardiac Tamponade 47 0.050
251
GNR003 Generalized Atherosclerosis 46 0.050
252
CRB004 Cerebral Artery Occlusion 45 0.050
253
P OCY003 Oocyte Maturation Defect 1 45 0.050
254
IMM064 Immunodeficiency, Common Variable, 10 44 0.050
255
HRT015 Heritable Pulmonary Arterial Hypertension 44 0.050
256
49X006 49, Xxxxy Syndrome 41 0.050
257
c MCR112 Microvascular Complications of Diabetes 2 41 0.050
258
P PRG092 Pregnancy Loss, Recurrent 1 40 0.050
259
CHL070 Cholesterol Embolism 39 0.050
260
c CHR682 Chronic Bilirubin Encephalopathy 39 0.050
261
c SYS043 Systemic Lupus Erythematosus 1 38 0.050
262
ACT167 Acute Generalized Exanthematous Pustulosis 37 0.050
263
SYS071 Systemic Autoimmune Disease 37 0.050
264
P ANT001 Anterolateral Myocardial Infarction 34 0.050
265
CRT008 Carotid Artery Dissection 33 0.050
266
HDR001 Hidrocystoma 31 0.050
267
DFF031 Diffuse Alveolar Hemorrhage 30 0.050
268
c HYP839 Hyperlipidemia, Familial Combined, 1 29 0.050
269
JVN026 Jeavons Syndrome 24 0.050
271
OST012 Osteoarthritis 78 0.041
272
P PRK057 Parkinson Disease, Late-Onset 78 0.041
273
P SCH015 Schizophrenia 74 0.041
274
P CNR004 Cone-Rod Dystrophy 2 73 0.041
275
SCH036 Scheie Syndrome 72 0.041
276
P MYP004 Myopathy 70 0.041
277
PLY001 Polycythemia Vera 69 0.041
278
SVR097 Severe Cutaneous Adverse Reaction 69 0.041
279
RCK004 Rickets 68 0.041
280
P HPT021 Hepatitis 67 0.041
281
c HMP029 Hemophilia a 67 0.041
282
MYL031 Myeloproliferative Neoplasm 66 0.041
283
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.041
284
P ART005 Arteriovenous Malformation 65 0.041
285
P VNW001 Von Willebrand's Disease 65 0.041
286
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.041
287
KWS002 Kawasaki Disease 65 0.041
288
GT001 Gout 64 0.041
289
ART002 Arts Syndrome 64 0.041
290
P PRD008 Periodontitis 64 0.041
291
P PSR002 Psoriasis 62 0.041
292
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.041
293
NTH001 Netherton Syndrome 60 0.041
294
HRP004 Herpes Zoster 60 0.041
295
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.041
296
P CTR002 Cataract 60 0.041
297
SPN027 Spinal Stenosis 59 0.041
298
P MYM013 Moyamoya Disease 1 57 0.041
299
P SLV026 Salivary Gland Carcinoma 57 0.041
300
P PLY018 Polycythemia 56 0.041
301
P SZR006 Seizure Disorder 56 0.041
302
GNR004 Generalized Anxiety Disorder 56 0.041
303
P ANT006 Antiphospholipid Syndrome 55 0.041
304
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.041
305
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.041
306
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.041
307
GLC003 Glucose Intolerance 54 0.041
308
P TRM003 Tremor 54 0.041
309
P RTN018 Retinal Disease 53 0.041
310
PST011 Pustulosis of Palm and Sole 52 0.041
311
ART074 Aortic Dissection 52 0.041
312
c VRL005 Viral Pneumonia 52 0.041
313
P MMB011 Membranous Nephropathy 50 0.041
314
c PRM012 Primary Polycythemia 50 0.041
315
c HYP603 Hyperoxaluria, Primary, Type Iii 50 0.041
316
P ESN008 Eosinophilic Pneumonia 50 0.041
317
c INF145 Infantile Liver Failure Syndrome 1 50 0.041
318
P ART018 Aortic Valve Insufficiency 49 0.041
319
c MTR002 Mitral Valve Insufficiency 48 0.041
320
P RNL015 Renal Hypertension 47 0.041
321
MYC005 Myocardial Stunning 46 0.041
322
P HRN001 Horner's Syndrome 45 0.041
323
HMR002 Hemarthrosis 45 0.041
324
CRT015 Carotid Artery Occlusion 45 0.041
325
BNM001 Bone Marrow Cancer 43 0.041
326
CYT002 Cytokine Deficiency 42 0.041
327
GST020 Gastric Antral Vascular Ectasia 41 0.041
328
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.041
329
RST023 Resting Heart Rate, Variation in 41 0.041
330
RDN001 Reading Disorder 40 0.041
331
THR035 Thrombasthenia 40 0.041
332
CRN020 Coronary Restenosis 39 0.041
333
MLG120 Malignant Migrating Partial Seizures of Infancy 39 0.041
334
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.041
335
P PST059 Pustular Psoriasis 37 0.041
336
c ACQ042 Acquired Hemophilia a 37 0.041
337
MDD003 Middle Cerebral Artery Infarction 36 0.041
338
THR123 Thrombotic Microangiopathy 36 0.041
340
INF013 Inferior Myocardial Infarction 33 0.041
341
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.041
342
HPT085 Hepatitis, Fulminant Viral 32 0.041
343
RNL001 Renal Artery Obstruction 31 0.041
344
FNT004 Fainting 30 0.041
345
CRD220 Cardiac Valvular Defect, Developmental 29 0.041
346
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.041
347
FTL073 Fetal Anticonvulsant Syndrome 26 0.041
348
ATR055 Atrial Septal Aneurysm 25 0.041
349
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.041
350
c CRN214 Coronary Heart Disease 5 24 0.041
351
INT074 Intracranial Arteriosclerosis 23 0.041
352
MNS002 Mini Stroke 19 0.041
353
MTS005 Metastatic Squamous Neck Cancer with Occult Primary 11 0.041
354
P HPT023 Hepatocellular Carcinoma 100 0.029
355
P BRS047 Breast Cancer 97 0.029
356
ESP021 Esophageal Cancer 90 0.029
357
P OVR042 Ovarian Cancer 88 0.029
358
P ATX030 Ataxia-Telangiectasia 82 0.029
359
c DLT002 Dilated Cardiomyopathy 79 0.029
360
PFF001 Pfeiffer Syndrome 79 0.029
361
BRN028 Brain Cancer 74 0.029
362
CRH001 Crohn's Disease 74 0.029
363
ULC004 Ulcerative Colitis 73 0.029
364
c SPN225 Spondyloarthropathy 1 73 0.029
365
P MLT020 Multiple Sclerosis 72 0.029
366
P EPL164 Epilepsy 71 0.029
367
P HYP061 Hypertrophic Cardiomyopathy 70 0.029
368
ABT001 Abetalipoproteinemia 69 0.029
369
P ANG001 Angelman Syndrome 69 0.029
370
P ESS003 Essential Thrombocythemia 68 0.029
371
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.029
372
STH001 Saethre-Chotzen Syndrome 67 0.029
373
P HYP098 Hypereosinophilic Syndrome 67 0.029
374
c FML021 Familial Hypercholesterolemia 66 0.029
375
GLN010 Glanzmann Thrombasthenia 66 0.029
376
ART001 Arterial Tortuosity Syndrome 66 0.029
377
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.029
378
AND002 Androgen Insensitivity Syndrome 66 0.029
379
P HYD006 Hydrocephalus 66 0.029
380
P NRV007 Nervous System Disease 66 0.029
381
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.029
382
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 65 0.029
383
PPL049 Papillon-Lefevre Syndrome 65 0.029
384
BRR014 Barrett Esophagus 65 0.029
385
IRR002 Irritable Bowel Syndrome 65 0.029
386
P PRS038 Personality Disorder 65 0.029
387
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.029
388
CRB011 Cerebrotendinous Xanthomatosis 65 0.029
389
P ANR048 Aniridia 1 63 0.029
390
P HYP069 Hyperparathyroidism 63 0.029
391
c MLG084 Malignant Fibrous Histiocytoma 63 0.029
392
P HYP055 Hypoplastic Left Heart Syndrome 63 0.029
393
c ACT068 Acute Cystitis 63 0.029
394
ANR007 Anorexia Nervosa 63 0.029
395
c HPT003 Hepatitis a 62 0.029
396
P HYP750 Hypertriglyceridemia, Familial 62 0.029
397
P TRC086 Trichohepatoenteric Syndrome 1 62 0.029
398
TXC005 Toxic Shock Syndrome 62 0.029
399
CHL068 Cholestasis 61 0.029
400
OST003 Osteonecrosis 61 0.029
401
FTT001 Fatty Liver Disease 61 0.029
402
c PNS012 Paine Syndrome 61 0.029
403
c SCL052 Scleroderma, Familial Progressive 61 0.029
404
P ENC018 Encephalopathy 61 0.029
405
RTN017 Retinal Detachment 61 0.029
406
APP008 Appendicitis 61 0.029
407
DCB001 Decubitus Ulcer 61 0.029
408
P NPH012 Nephrotic Syndrome 60 0.029
409
c LPM012 Lipomatosis, Multiple 60 0.029
410
ACN002 Acanthosis Nigricans 60 0.029
411
ING001 Inguinal Hernia 60 0.029
412
INS001 Insulinoma 60 0.029
413
P AXN002 Axenfeld-Rieger Syndrome 59 0.029
414
VSL002 Visual Epilepsy 59 0.029
415
BRN002 Bronchiolitis 59 0.029
416
GST045 Gastroenteritis 59 0.029
417
P PLY017 Polyarteritis Nodosa 58 0.029
418
P ANP001 Anaplastic Large Cell Lymphoma 58 0.029
419
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.029
420
c PRM005 Primary Hyperparathyroidism 58 0.029
421
ERY003 Erythema Multiforme 58 0.029
422
P PRP019 Peripheral Nervous System Disease 58 0.029
423
IRN002 Iron Metabolism Disease 57 0.029
424
VSC002 Vascular Dementia 57 0.029
425
CYT008 Cytomegalovirus Infection 57 0.029
426
INT303 Intracranial Hypertension, Idiopathic 57 0.029
427
ENH001 Enhanced S-Cone Syndrome 57 0.029
428
PNM008 Pneumothorax 56 0.029
429
P MYS005 Myositis 56 0.029
430
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.029
431
VSC016 Vasculopathy, Retinal, with Cerebral Leukodystrophy 56 0.029
432
MCR141 Mucormycosis 56 0.029
433
SLC006 Silicosis 56 0.029
434
BRN012 Bronchiolitis Obliterans 55 0.029
435
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.029
436
P STR020 Strabismus 55 0.029
437
P ALP106 Alport Syndrome 1, X-Linked 55 0.029
438
P VNS003 Venous Insufficiency 55 0.029
439
P DBT005 Diabetes Insipidus 55 0.029
440
ESN005 Eosinophilic Gastroenteritis 55 0.029
441
HYP060 Hyperinsulinism 54 0.029
442
P RST001 Restless Legs Syndrome 54 0.029
443
GST037 Gastroparesis 54 0.029
444
THR013 Thoracic Outlet Syndrome 54 0.029
445
P INF037 Inflammatory Bowel Disease 54 0.029
446
PRC013 Pericarditis 54 0.029
447
SNS003 Sensory Peripheral Neuropathy 54 0.029
448
DNT005 Dentatorubral-Pallidoluysian Atrophy 54 0.029
449
CLL003 Cellulitis 54 0.029
450
P LCH002 Lichen Planus 53 0.029
451
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.029
452
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.029
453
P SHR001 Short Bowel Syndrome 53 0.029
454
P CTN003 Cutaneous Lupus Erythematosus 53 0.029
455
HMC014 Homocysteinemia 53 0.029
456
INT075 Intracranial Hypertension 53 0.029
457
c HPT007 Hepatitis E 53 0.029
458
ALC009 Alcoholic Liver Cirrhosis 53 0.029
459
STT041 Stuttering 52 0.029
460
c VRL010 Viral Hepatitis 52 0.029
461
P RCT021 Rectum Cancer 52 0.029
462
IMP005 Impotence 52 0.029
463
ILS001 Ileus 51 0.029
464
SPN019 Spondylolisthesis 51 0.029
465
P PRC012 Pericardial Effusion 51 0.029
466
P INT099 Intrahepatic Cholestasis of Pregnancy 51 0.029
467
P CHL066 Cholangitis 51 0.029
468
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.029
469
HNT002 Hantavirus Pulmonary Syndrome 50 0.029
470
PRT018 Portal Vein Thrombosis 50 0.029
471
c THR071 Thrombocytopenia 1 50 0.029
472
MTB004 Metabolic Acidosis 50 0.029
473
ENT004 Enthesopathy 49 0.029
474
PPL021 Papilledema 49 0.029
475
c CHR431 Chronic Venous Insufficiency 49 0.029
476
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.029
477
INT078 Intracranial Thrombosis 49 0.029
478
DDN006 Duodenitis 49 0.029
479
P CMP008 Compartment Syndrome 49 0.029
480
QDR001 Quadriplegia 48 0.029
481
RGH001 Right Bundle Branch Block 48 0.029
482
PTC002 Potocki-Lupski Syndrome 48 0.029
483
SPL018 Splenomegaly 48 0.029
484
IGG001 Iga Glomerulonephritis 48 0.029
485
HMP001 Hemopericardium 48 0.029
486
ART004 Aortic Atherosclerosis 47 0.029
487
HLX001 Helix Syndrome 47 0.029
488
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.029
489
c HYD019 Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius 47 0.029
490
P PRR002 Pure Red-Cell Aplasia 47 0.029
491
MLT152 Multiple Self-Healing Squamous Epithelioma 47 0.029
492
PRC003 Proctitis 47 0.029
493
RNL077 Renal Fibrosis 47 0.029
494
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.029
495
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.029
496
ANT003 Antley-Bixler Syndrome 47 0.029
497
RTN020 Retinal Vascular Disease 46 0.029
498
P HMR005 Hemorrhoid 46 0.029
499
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 46 0.029
500
P PRD037 Periodontal Ehlers-Danlos Syndrome 45 0.029
501
SYN036 Syncope 45 0.029
502
DST006 Diastolic Heart Failure 45 0.029
503
PRL008 Paralytic Ileus 45 0.029
504
PLN005 Palindromic Rheumatism 45 0.029
505
DNB001 Danubian Endemic Familial Nephropathy 44 0.029
506
P SDR002 Siderosis 44 0.029
507
ESP018 Esophageal Candidiasis 44 0.029
508
MND023 Mend Syndrome 43 0.029
509
DVR002 Diverticulitis 43 0.029
510
RDC006 Red Cell Aplasia 43 0.029
511
PLM019 Pleomorphic Liposarcoma 43 0.029
512
DRG002 Drug-Induced Hepatitis 43 0.029
513
DRG024 Drug Allergy 42 0.029
514
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.029
515
MCH006 Mechanical Strabismus 42 0.029
516
JWD001 Jawad Syndrome 40 0.029
517
SPR126 Superior Semicircular Canal Dehiscence 40 0.029
518
ART008 Arteriosclerosis Obliterans 40 0.029
519
MLT001 Multiple Chemical Sensitivity 40 0.029
520
c ACQ005 Acquired Thrombocytopenia 39 0.029
521
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.029
522
SPR066 Superficial Siderosis 39 0.029
523
CHL039 Choledocholithiasis 38 0.029
524
OPT010 Optic Papillitis 38 0.029
525
TRC005 Tracheal Stenosis 38 0.029
526
SWL001 Swallowing Disorders 38 0.029
527
CRB009 Cerebritis 37 0.029
528
GLM044 Glomerular Disease 37 0.029
529
PHM001 Phimosis 37 0.029
530
SPN331 Spondyloocular Syndrome 36 0.029
531
LVD003 Livedoid Vasculitis 36 0.029
532
FXD003 Fixed Drug Eruption 35 0.029
533
END072 Endotheliitis 35 0.029
534
ACT149 Acetaminophen Metabolism 35 0.029
535
c TWN011 Townes-Brocks Syndrome 1 35 0.029
536
ATX010 Ataxia Neuropathy Spectrum 34 0.029
537
c CHR087 Chronic Cystitis 34 0.029
538
AMR003 Amaurosis Fugax 34 0.029
539
c INT059 Internal Hemorrhoid 34 0.029
540
PLT015 Platelet Aggregation, Spontaneous 34 0.029
541
c RST012 Restless Legs Syndrome 1 34 0.029
542
ALR002 Al-Raqad Syndrome 33 0.029
543
ACT064 Acute Necrotizing Encephalitis 33 0.029
544
PHN011 Phenytoin Toxicity 33 0.029
545
c SBC035 Subacute Cutaneous Lupus Erythematosus 32 0.029
546
SBC014 Subclavian Steal Syndrome 32 0.029
547
c BLD140 Blood Group, I System 32 0.029
548
HYD048 Hydrocephalus with Stenosis of the Aqueduct of Sylvius 32 0.029
549
FMR003 Femoral Neuropathy 31 0.029
550
ERY066 Erythema Multiforme Major 30 0.029
551
ASP036 Aspirin Allergy 30 0.029
552
ENG004 Engraftment Syndrome 30 0.029
553
MTY003 Mutyh Polyposis 30 0.029
554
MYC088 Mycobacterium Avium Complex Infections 29 0.029
555
CTN019 Cutaneous Polyarteritis Nodosa 27 0.029
556
OTL001 Outlet Dysfunction Constipation 27 0.029
557
c ACQ016 Acquired Pure Red Cell Aplasia 27 0.029
558
CND001 Conidiobolomycosis 26 0.029
559
c BRN145 Bronchiectasis 3 25 0.029
560
MXD010 Mixed Epithelial Stromal Tumour 24 0.029
561
BLD163 Blood Group, Dombrock System 24 0.029
562
HYP049 Hypertrophy of Tongue Papillae 24 0.029
563
c RRH015 Rare Hemorrhagic Disorder 23 0.029
564
AGN004 Aganglionosis, Total Intestinal 22 0.029
565
ATR024 Atrial Fibrillation and Stroke 22 0.029
566
PLL009 Pellucid Marginal Degeneration 22 0.029
567
ANG012 Angiodysplasia of Intestine 21 0.029
568
PDT041 Pediatric Arterial Ischemic Stroke 19 0.029
569
AND005 Androgen Insensitivity Syndrome, Mild 19 0.029
570
DRG017 Drug-Induced Vasculitis 17 0.029
571
HDC005 Headache Associated with Sexual Activity 17 0.029
572
BLD137 Blood Group--Ahonen 16 0.029
573
c EST011 Esterase C 15 0.029
Content
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