Search results for Atenolol

317 hits were found for Atenolol

# Family MCID Name MIFTS Score
1
PRP027 Peripheral Vascular Disease 68 0.187
2
c HYP595 Hypertension, Essential 69 0.170
3
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.155
4
VSC007 Vascular Disease 67 0.139
5
ATN002 Autonomic Nervous System Disease 48 0.115
6
PRP080 Peripheral Artery Disease 37 0.115
7
MRF001 Marfan Syndrome 73 0.104
8
P HRT032 Heart Disease 75 0.098
9
ANG054 Angina Pectoris 50 0.098
10
P MYC007 Myocardial Infarction 79 0.092
11
ART017 Aortic Disease 57 0.085
12
HYP540 Hypertension, Diastolic 39 0.085
13
c CRN175 Coronary Heart Disease 4 19 0.085
14
CNG034 Congestive Heart Failure 72 0.078
15
P CRD011 Cardiomyopathy 68 0.078
16
HYP006 Hypertensive Heart Disease 50 0.078
17
PRD011 Proud Syndrome 42 0.078
18
ABR009 Abruzzo-Erickson Syndrome 38 0.078
19
c CNG031 Congenital Nervous System Abnormality 37 0.078
20
P CRN178 Coronary Heart Disease 6 21 0.078
21
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.069
22
P CRN211 Coronary Artery Disease 74 0.069
23
P ATR011 Atrial Fibrillation 66 0.069
24
CNN005 Connective Tissue Disease 62 0.069
25
ISC004 Ischemia 61 0.069
26
CHL071 Child Syndrome 58 0.069
27
ART111 Artery Disease 55 0.069
28
PRP019 Peripheral Nervous System Disease 55 0.069
29
KDS001 Kid Syndrome 53 0.069
30
ADL002 Adult Syndrome 52 0.069
31
ALL026 Allergic Hypersensitivity Disease 52 0.069
32
ATR060 Atrial Standstill, Digenic 51 0.069
33
INT007 Intermediate Coronary Syndrome 50 0.069
34
ATN005 Autonomic Dysfunction 49 0.069
35
MSS002 Mass Syndrome 48 0.069
36
P MRD002 Marden-Walker Syndrome 46 0.069
37
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.069
38
GLC008 Glucose Metabolism Disease 42 0.069
39
CNT099 Contractural Arachnodactyly, Congenital 40 0.069
40
BND014 Bone Development Disease 40 0.069
41
ALR002 Al-Raqad Syndrome 36 0.069
42
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 35 0.069
43
ACR002 Acrocapitofemoral Dysplasia 33 0.069
44
c CRN214 Coronary Heart Disease 5 22 0.069
45
c CRN172 Coronary Heart Disease 3 19 0.069
46
c HYP454 Hypertension, Essential 8 16 0.069
47
ART016 Aortic Aneurysm 69 0.060
48
ISC006 Ischemic Heart Disease 68 0.060
49
BRC012 Brucellosis 66 0.060
50
LPD008 Lipid Metabolism Disorder 58 0.060
51
c FML001 Familial Atrial Fibrillation 58 0.060
52
P HYP060 Hyperinsulinism 58 0.060
53
P MSC007 Muscle Hypertrophy 58 0.060
54
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.060
55
P CHR345 Chronic Pain 50 0.060
56
DST006 Diastolic Heart Failure 46 0.060
57
VSC047 Vascular Malformation 45 0.060
58
VNT011 Ventricular Fibrillation, Familial, 1 41 0.060
59
P ABD016 Abdominal Obesity-Metabolic Syndrome 41 0.060
60
CHR413 Chronic Myocardial Ischemia 41 0.060
61
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.060
62
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.060
63
MSC004 Muscle Tissue Disease 34 0.060
64
CRD016 Cardiac Rupture 34 0.060
65
CHR476 Chronic Angina 26 0.060
66
c CRN173 Coronary Heart Disease 8 18 0.060
67
c CNG385 Congenital Heart Defects, Multiple Types, 3 17 0.060
68
CRN073 Coronary Arteries Congenital Malformation 10 0.060
69
P OBS005 Obesity 92 0.049
70
P PLM037 Pulmonary Hypertension 79 0.049
71
c DLT002 Dilated Cardiomyopathy 76 0.049
72
STR067 Stroke, Ischemic 75 0.049
73
P MYP004 Myopathy 67 0.049
74
P KDN018 Kidney Disease 66 0.049
75
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.049
76
ATH003 Atherosclerosis 65 0.049
77
CRB039 Cerebrovascular Disease 63 0.049
78
P CRD194 Cardiomyopathy, Familial Hypertrophic 62 0.049
79
HYP056 Hypoglycemia 61 0.049
80
c ACT075 Acute Myocardial Infarction 60 0.049
81
c ADL017 Adult T-Cell Leukemia 60 0.049
82
P DRR001 Diarrhea 60 0.049
83
KRT001 Keratoconjunctivitis Sicca 59 0.049
84
P HMN010 Hemangioma 59 0.049
85
WLL006 Wells Syndrome 59 0.049
86
ART021 Arteriosclerosis 58 0.049
87
P CMR001 Camurati-Engelmann Disease 58 0.049
88
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 57 0.049
89
CTS003 Coats Disease 57 0.049
90
ABL002 Ablepharon-Macrostomia Syndrome 57 0.049
91
THR024 Thrombosis 57 0.049
92
CRT016 Carotid Artery Disease 57 0.049
93
ANR040 Aneurysm 57 0.049
94
END030 End Stage Renal Failure 55 0.049
95
c ART101 Aortic Valve Disease 2 53 0.049
96
SLP005 Sleep Disorder 53 0.049
97
KRT006 Keratoconjunctivitis 52 0.049
98
P MSC033 Muscle Disorders 52 0.049
99
P CPL006 Capillary Hemangioma 51 0.049
100
VSC006 Vascular Cancer 51 0.049
101
c ART115 Aortic Valve Disease 1 50 0.049
102
ATR057 Atrioventricular Block 49 0.049
103
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.049
104
c VNT013 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1 48 0.049
105
OCL006 Ocular Hypertension 48 0.049
106
P TRC086 Trichohepatoenteric Syndrome 1 48 0.049
107
P RNL015 Renal Hypertension 48 0.049
108
VND001 Vein Disease 47 0.049
109
PRP021 Peripheral Nervous System Neoplasm 46 0.049
110
HRT007 Heart Cancer 46 0.049
111
BLD053 Blood Platelet Disease 46 0.049
112
ADR038 Adermatoglyphia 46 0.049
113
GDS001 Good Syndrome 44 0.049
114
CRD118 Cardiovascular Cancer 44 0.049
115
BNN003 Bone Inflammation Disease 44 0.049
116
SYS003 Systolic Heart Failure 43 0.049
117
RNL097 Renal Artery Disease 43 0.049
118
DRR008 Diarrhea 1, Secretory Chloride, Congenital 42 0.049
119
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.049
120
P BLD051 Blood Coagulation Disease 42 0.049
121
BRN080 Brain Ischemia 41 0.049
122
c HMN027 Hemangioma, Capillary Infantile 41 0.049
123
HRT012 Heart Valve Disease 40 0.049
124
ATN003 Autonomic Nervous System Neoplasm 40 0.049
125
SKN018 Skin Hemangioma 39 0.049
126
P HRT035 Heart Block, Congenital 38 0.049
127
MDY003 Mody, Type Ii 36 0.049
128
CPL005 Capillary Disease 36 0.049
129
c CRD199 Cardiomyopathy, Hypertrophic 6 36 0.049
130
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 36 0.049
131
CPL011 Capillary Malformations, Congenital, 1, Somatic, Mosaic 35 0.049
132
c ACT020 Acute T Cell Leukemia 35 0.049
133
GLB003 Globe Disease 32 0.049
134
P HRT017 Heart Tumor 32 0.049
135
WSM002 Waisman Syndrome 32 0.049
136
KDN013 Kidney Hypertrophy 31 0.049
137
CVT001 Cavitary Optic Disc Anomalies 31 0.049
138
MDY005 Mody, Type I 30 0.049
139
c CRD207 Cardiomyopathy, Hypertrophic, 3 30 0.049
140
c PLM127 Pulmonary Hypertension, Primary, 3 28 0.049
141
c PLM128 Pulmonary Hypertension, Primary, 2 28 0.049
142
c MYC058 Myocardial Infarction 2 28 0.049
143
CRB031 Cerebral Arterial Disease 27 0.049
144
c CNG478 Congenital Diarrhea 25 0.049
145
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.049
146
SNG003 Single Ventricular Heart 22 0.049
147
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 21 0.049
148
c CRN174 Coronary Heart Disease 2 20 0.049
149
VSC009 Vascular Skin Disease 19 0.049
150
LMB013 Limb Reduction Defect 16 0.049
151
HRT029 Heart Tumor of the Child 15 0.049
152
PRP050 Peripheral Arterial Occlusive Disease 1 14 0.049
153
BLN008 Blind Hypotensive Eye 14 0.049
154
STR005 Stork Bite 13 0.049
155
HRD059 Hereditary Peripheral Nervous Disorder 11 0.049
156
P ALZ034 Alzheimer Disease 92 0.035
157
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.035
158
P HYP607 Hypercholesterolemia, Familial 76 0.035
159
P INF038 Influenza 72 0.035
160
P NRV007 Nervous System Disease 71 0.035
161
P PRK057 Parkinson Disease, Late-Onset 70 0.035
162
PCK002 Pick Disease 68 0.035
163
PSY004 Psychotic Disorder 67 0.035
164
LVR012 Liver Cirrhosis 67 0.035
165
c CHR089 Chronic Kidney Failure 66 0.035
166
ATP002 Atopy 66 0.035
167
P KDN017 Kidney Cancer 65 0.035
168
DMN002 Dementia 65 0.035
169
P ORT004 Orthostatic Intolerance 64 0.035
170
DFC004 Deficiency Anemia 64 0.035
171
LNG099 Lung Disease 64 0.035
172
P OST002 Osteoporosis 64 0.035
173
PRT036 Peritonitis 63 0.035
174
CRD119 Cardiac Arrest 61 0.035
175
P HYP117 Hypertriglyceridemia 61 0.035
176
HYP066 Hyperglycemia 61 0.035
177
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 60 0.035
178
P PRT013 Portal Hypertension 60 0.035
179
P NRV006 Nervous System Cancer 60 0.035
180
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.035
181
c CNT035 Central Nervous System Disease 60 0.035
182
P ORL007 Oral Cavity Cancer 59 0.035
183
OCL009 Ocular Cancer 59 0.035
184
P ENC018 Encephalopathy 59 0.035
185
P NRP001 Neuropathy 59 0.035
186
P INF032 Infertility 59 0.035
187
MRB003 Morbid Obesity 58 0.035
188
ADN018 Adenoma 58 0.035
189
P MTR012 Mitral Valve Disease 58 0.035
190
P THR003 Thoracic Aortic Aneurysm 57 0.035
191
PST028 Post-Traumatic Stress Disorder 57 0.035
192
c PRC016 Pre-Eclampsia 56 0.035
193
PTT006 Pituitary Adenoma 56 0.035
194
P FRS003 Fraser Syndrome 56 0.035
195
GLC003 Glucose Intolerance 55 0.035
196
P CDS001 Cadasil 55 0.035
197
c THR092 Thrombophilia Due to Thrombin Defect 54 0.035
198
c PND001 Pain Disorder 54 0.035
199
P MMB011 Membranous Nephropathy 54 0.035
200
VSC002 Vascular Dementia 54 0.035
201
P MCR129 Microvascular Complications of Diabetes 1 54 0.035
202
CND002 Conduct Disorder 54 0.035
203
P ECL001 Eclampsia 54 0.035
204
C3D001 C3 Deficiency 53 0.035
205
DSS008 Disease of Mental Health 52 0.035
206
P ANG015 Angioedema 52 0.035
207
P SPS003 Spastic Diplegia 52 0.035
208
MYC002 Mycobacterium Avium Complex Disease 52 0.035
209
c PRK031 Parkinson Disease 1 51 0.035
210
P PRC031 Preeclampsia/eclampsia 1 51 0.035
211
IMM136 Immune System Disease 51 0.035
212
CRN030 Coronary Stenosis 51 0.035
213
RTN023 Retinitis 50 0.035
214
BNF002 Bone Fracture 50 0.035
215
URN009 Urinary System Disease 50 0.035
216
INT075 Intracranial Hypertension 50 0.035
217
OVR063 Overnutrition 50 0.035
218
P SCK002 Sick Sinus Syndrome 50 0.035
219
P URF003 Urofacial Syndrome 1 50 0.035
220
PRN021 Paranasal Sinus Disease 49 0.035
221
NCT008 Nicotine Dependence, Protection Against 49 0.035
222
P CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 48 0.035
223
ACT017 Acute Chest Syndrome 48 0.035
224
NSD001 Nose Disease 48 0.035
225
c MLG069 Malignant Hypertension 47 0.035
226
CRB025 Carbohydrate Metabolic Disorder 46 0.035
227
ART004 Aortic Atherosclerosis 46 0.035
228
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.035
229
GLT021 Glutaricaciduria, Type I 46 0.035
230
c MCR113 Microvascular Complications of Diabetes 3 45 0.035
231
CRB004 Cerebral Artery Occlusion 45 0.035
232
ACR041 Acromelic Frontonasal Dysostosis 45 0.035
233
ATN004 Autonomic Neuropathy 45 0.035
234
ACD009 Acid-Labile Subunit, Deficiency of 45 0.035
235
P ABD003 Abdominal Aortic Aneurysm 45 0.035
236
ALN001 Aland Island Eye Disease 45 0.035
237
P DYS021 Dysautonomia 44 0.035
238
LFT009 Left Ventricular Outflow Tract Obstruction 43 0.035
239
PHY002 Physical Disorder 43 0.035
240
CRT015 Carotid Artery Occlusion 43 0.035
241
BRT030 Birth Defects 43 0.035
242
ACT058 Active Peptic Ulcer Disease 43 0.035
243
MTR003 Mitral Valve Stenosis 43 0.035
244
SNS023 Sensory System Cancer 43 0.035
245
PRD004 Prediabetes Syndrome 43 0.035
246
CRB008 Cerebral Atherosclerosis 43 0.035
247
SXL003 Sexual Disorder 42 0.035
248
PTY001 Pityriasis Rosea 42 0.035
249
CRB047 Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy 41 0.035
250
SPC005 Speech Disorder 41 0.035
251
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 41 0.035
252
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.035
253
ACT084 Acute Stress Disorder 40 0.035
254
CRN019 Coronary Artery Vasospasm 40 0.035
255
c CHR096 Chronic Pulmonary Heart Disease 40 0.035
256
BRN118 Brain Small Vessel Disease with or Without Ocular Anomalies 40 0.035
257
ATS008 Autosomal Dominant Disease 39 0.035
258
CRB009 Cerebritis 39 0.035
259
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 39 0.035
260
RTR011 Retroperitoneal Fibrosis 39 0.035
261
P FML187 Familial Hypertension 38 0.035
262
NSL022 Nasal Cavity Disease 38 0.035
263
OCL010 Ocular Hypotension 38 0.035
264
ADJ001 Adjustment Disorder 38 0.035
265
c PRK030 Parkinson Disease 4 38 0.035
266
DRG001 Drug Psychosis 38 0.035
267
BLD054 Blood Protein Disease 37 0.035
268
GNR003 Generalized Atherosclerosis 37 0.035
269
AMY002 Amyloid Tumor 37 0.035
270
BNS002 Bone Structure Disease 37 0.035
271
ISC005 Ischemic Bone Disease 36 0.035
272
NTR005 Nutritional Deficiency Disease 36 0.035
273
SNT005 Sinoatrial Node Disease 36 0.035
274
IMP003 Impaired Renal Function Disease 34 0.035
275
ANG049 Angioedema Induced by Ace Inhibitors 34 0.035
276
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 33 0.035
277
PLC008 Placenta Disease 33 0.035
278
HYP114 Hypertensive Nephropathy 33 0.035
279
SBV001 Subvalvular Aortic Stenosis 31 0.035
280
c SCK017 Sick Sinus Syndrome 1 29 0.035
281
PRM243 Primary Bone Cancer 29 0.035
282
DBT081 Diabetic Encephalopathy 28 0.035
283
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.035
284
c ATR038 Atrial Fibrillation, Familial, 3 27 0.035
285
TYP027 Type 1 Diabetes Mellitus 10 27 0.035
286
PST048 Postural Orthostatic Tachycardia Syndrome 27 0.035
287
c ATR061 Atrial Fibrillation, Familial, 10 26 0.035
288
c CNG404 Congenital Heart Defects, Multiple Types, 4 26 0.035
289
c ATR039 Atrial Fibrillation, Familial, 4 26 0.035
290
SNT004 Sinoatrial Node Dysfunction and Deafness 25 0.035
291
EYC003 Eye Accommodation Disease 24 0.035
292
c SCK022 Sick Sinus Syndrome 3 22 0.035
293
ATR024 Atrial Fibrillation and Stroke 22 0.035
294
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 21 0.035
295
CRB087 Cerebral Arteriosclerosis 21 0.035
296
BNR002 Bone Resorption Disease 21 0.035
297
CMB002 Combat Disorder 21 0.035
298
c CDS005 Cadasil 2 20 0.035
299
c ATR026 Atrial Fibrillation, Familial, 1 20 0.035
300
c CRN177 Coronary Heart Disease 7 20 0.035
301
ACT228 Acute Radiation Syndrome 20 0.035
302
c CRN176 Coronary Heart Disease 9 18 0.035
303
ATN001 Autonomic Peripheral Neuropathy 17 0.035
304
c ADL079 Adult Heart Tumor 16 0.035
305
c DYS033 Dysautonomia Like Disorder 16 0.035
306
c ATR025 Atrial Fibrillation, Familial, 2 16 0.035
307
BNM008 Bone Mineral Density, Low 16 0.035
308
c INF136 Influenza, Severe 15 0.035
309
c ATR027 Atrial Fibrillation, Familial, 5 15 0.035
310
AQG001 Aquagenic Pruritus 15 0.035
311
LWR014 Lower Limb Hypertrophy 15 0.035
312
UPP009 Upper Limb Hypertrophy 14 0.035
313
INT074 Intracranial Arteriosclerosis 14 0.035
314
CRN207 Coronary Sinus Stenosis 13 0.035
315
DMN012 Dementia - Subcortical 13 0.035
316
SGM003 Segmentation Syndrome 1 12 0.035
317
c CDS004 Cadasil 1 12 0.035
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