Search results for Atenolol

306 hits were found for Atenolol

# Family MCID Name MIFTS Score
1
c HYP595 Hypertension, Essential 84 0.672
2
ANG054 Angina Pectoris 66 0.419
3
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.223
4
LPP008 Lipoprotein Quantitative Trait Locus 62 0.223
5
ART140 Arteries, Anomalies of 52 0.205
6
P CRN300 Coronary Heart Disease 1 63 0.201
7
RST023 Resting Heart Rate, Variation in 41 0.198
8
MRF001 Marfan Syndrome 77 0.195
9
c ACT075 Acute Myocardial Infarction 57 0.181
10
ISC004 Ischemia 58 0.170
11
P MYC007 Myocardial Infarction 70 0.153
12
P CRD246 Cardiovascular System Disease 57 0.153
13
HYP056 Hypoglycemia 66 0.149
14
P VSC007 Vascular Disease 63 0.149
15
STR067 Stroke, Ischemic 81 0.145
16
P TRM003 Tremor 54 0.145
17
P HRT032 Heart Disease 75 0.140
18
P KDN018 Kidney Disease 72 0.140
19
CNG034 Congestive Heart Failure 69 0.140
20
HYP005 Hypokalemia 55 0.140
21
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.135
22
CRB039 Cerebrovascular Disease 67 0.135
23
MRD002 Marden-Walker Syndrome 56 0.135
24
HYP540 Hypertension, Diastolic 40 0.135
25
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.130
26
MSC007 Muscle Hypertrophy 64 0.130
27
P HMN010 Hemangioma 61 0.130
28
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.130
29
P HYP061 Hypertrophic Cardiomyopathy 70 0.125
30
P MTR003 Mitral Valve Stenosis 50 0.125
31
c MGR028 Migraine with or Without Aura 1 67 0.120
32
INT007 Intermediate Coronary Syndrome 55 0.120
33
ART074 Aortic Dissection 52 0.120
34
ATX019 Ataxia with Vitamin E Deficiency 42 0.120
35
c ATR087 Atrial Standstill 1 75 0.114
36
P ATR011 Atrial Fibrillation 66 0.114
37
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.108
38
CNN005 Connective Tissue Disease 68 0.108
39
ATH013 Atherosclerosis Susceptibility 65 0.108
40
c PRC016 Pre-Eclampsia 63 0.108
41
LPD008 Lipid Metabolism Disorder 62 0.108
42
P HDC001 Headache 57 0.108
43
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.108
44
RTR011 Retroperitoneal Fibrosis 40 0.108
45
ALL026 Allergic Hypersensitivity Disease 62 0.102
46
LNG099 Lung Disease 60 0.102
47
P EXN002 Exanthem 57 0.102
48
c MCR113 Microvascular Complications of Diabetes 3 52 0.102
49
P ART018 Aortic Valve Insufficiency 49 0.102
50
c MCR120 Microvascular Complications of Diabetes 7 47 0.102
51
c MCR130 Microvascular Complications of Diabetes 6 41 0.102
52
c MCR133 Microvascular Complications of Diabetes 4 41 0.102
53
48X005 48,xyyy 39 0.102
54
AST005 Asthma 76 0.096
55
c HYP836 Hypercholesterolemia, Familial, 1 73 0.096
56
ART016 Aortic Aneurysm 69 0.096
57
c RHB024 Rhabdomyosarcoma 2 67 0.096
58
P MCR115 Microvascular Complications of Diabetes 5 66 0.096
59
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.096
60
P HYP750 Hypertriglyceridemia, Familial 62 0.096
61
P DRR001 Diarrhea 55 0.096
62
WTH001 Withdrawal Disorder 48 0.096
63
ANX010 Anxiety 73 0.089
64
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.089
65
P CRD119 Cardiac Arrest 67 0.089
66
HYP066 Hyperglycemia 61 0.089
67
CRD223 Cardiac Arrhythmia 60 0.089
68
ANR040 Aneurysm 59 0.089
69
P HYP076 Hyperthyroidism 55 0.089
70
OCL006 Ocular Hypertension 53 0.089
71
PRP027 Peripheral Vascular Disease 71 0.081
72
DWN001 Down Syndrome 70 0.081
73
ADL002 Adult Syndrome 70 0.081
74
P TRN020 Turner Syndrome 67 0.081
75
IMP005 Impotence 52 0.081
76
P CPL006 Capillary Hemangioma 51 0.081
77
END086 End Stage Renal Disease 51 0.081
78
c HNT004 Huntington Disease-Like 2 50 0.081
79
CRN030 Coronary Stenosis 50 0.081
80
c CPL013 Capillary Malformations, Congenital 50 0.081
81
SCL003 Social Phobia 48 0.081
82
P RNL015 Renal Hypertension 47 0.081
83
SYN036 Syncope 45 0.081
84
c DLT002 Dilated Cardiomyopathy 79 0.072
85
P CNR004 Cone-Rod Dystrophy 2 73 0.072
86
c CHR684 Chronic Kidney Disease 70 0.072
87
c MCR129 Microvascular Complications of Diabetes 1 66 0.072
88
c FML001 Familial Atrial Fibrillation 65 0.072
89
P DBT009 Diabetes Mellitus 64 0.072
90
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.072
91
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.072
92
P ORT004 Orthostatic Intolerance 62 0.072
93
LVR012 Liver Cirrhosis 62 0.072
94
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.072
95
P ALC033 Alcohol Use Disorder 58 0.072
96
CNS004 Constipation 58 0.072
97
ATR057 Atrioventricular Block 55 0.072
98
P SCK002 Sick Sinus Syndrome 55 0.072
99
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.072
100
P ECL001 Eclampsia 50 0.072
101
P OPN001 Open-Angle Glaucoma 49 0.072
102
c MTR002 Mitral Valve Insufficiency 48 0.072
103
c MCR112 Microvascular Complications of Diabetes 2 41 0.072
104
c HNT011 Huntington Disease-Like 3 38 0.072
105
P FML187 Familial Hypertension 37 0.072
106
CHL079 Children's Interstitial Lung Disease 26 0.072
107
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.063
108
DFC004 Deficiency Anemia 70 0.063
109
P LVR013 Liver Disease 68 0.063
110
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 68 0.063
111
BRN024 Bronchitis 68 0.063
112
P PRS038 Personality Disorder 65 0.063
113
GT001 Gout 64 0.063
114
INT002 Intermittent Claudication 61 0.063
115
P LPS004 Lupus Erythematosus 61 0.063
116
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.063
117
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.063
118
THR024 Thrombosis 57 0.063
119
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.063
120
HYP266 Hypoxia 57 0.063
121
P ANG015 Angioedema 57 0.063
122
c ESS001 Essential Tremor 56 0.063
123
P NRP001 Neuropathy 56 0.063
124
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.063
125
AGN016 Aging 56 0.063
126
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.063
127
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.063
128
PLC008 Placenta Disease 50 0.063
129
SYS003 Systolic Heart Failure 49 0.063
130
HYP006 Hypertensive Heart Disease 49 0.063
131
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.063
132
c MLG069 Malignant Hypertension 47 0.063
133
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.063
134
CRD137 Cardiogenic Shock 47 0.063
135
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.063
136
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.063
137
c DRR009 Diarrhea 6 46 0.063
138
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.063
139
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.063
140
SBC016 Subacute Delirium 44 0.063
141
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.063
142
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.063
143
GST020 Gastric Antral Vascular Ectasia 41 0.063
144
C1N001 C1 Inhibitor Deficiency 39 0.063
145
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.063
146
P PRC031 Preeclampsia/eclampsia 1 38 0.063
147
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.063
148
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.063
149
c ART115 Aortic Valve Disease 1 75 0.051
150
LPT014 Leptin Deficiency or Dysfunction 74 0.051
151
P OST002 Osteoporosis 74 0.051
152
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.051
153
P PHC003 Pheochromocytoma 71 0.051
154
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 0.051
155
PSY004 Psychotic Disorder 67 0.051
156
P LNG028 Long Qt Syndrome 66 0.051
157
ALC007 Alcohol Dependence 66 0.051
158
c ART101 Aortic Valve Disease 2 65 0.051
159
IRR002 Irritable Bowel Syndrome 65 0.051
160
HYP020 Hyperprolactinemia 64 0.051
161
c FNC043 Fanconi Anemia, Complementation Group E 62 0.051
162
P VSC011 Vasculitis 62 0.051
163
NTR005 Nutritional Deficiency Disease 62 0.051
164
CHL068 Cholestasis 61 0.051
165
CHR066 Chronic Fatigue Syndrome 61 0.051
166
ING001 Inguinal Hernia 60 0.051
167
STT001 Status Epilepticus 60 0.051
168
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.051
169
PRT058 Pure Autonomic Failure 59 0.051
170
PST028 Post-Traumatic Stress Disorder 58 0.051
171
CRD132 Cardiac Conduction Defect 58 0.051
172
DSS008 Disease of Mental Health 58 0.051
173
P PRP019 Peripheral Nervous System Disease 58 0.051
174
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.051
175
c GRV008 Graves Disease 1 56 0.051
176
c FML035 Familial Hyperlipidemia 55 0.051
177
KRT006 Keratoconjunctivitis 53 0.051
178
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.051
179
PRP080 Peripheral Artery Disease 53 0.051
180
OCL069 Ocular Motor Apraxia 51 0.051
181
CHR515 Chronic Atrial and Intestinal Dysrhythmia 50 0.051
182
KRT001 Keratoconjunctivitis Sicca 49 0.051
183
ART017 Aortic Disease 49 0.051
184
SNT005 Sinoatrial Node Disease 49 0.051
185
BNR002 Bone Resorption Disease 48 0.051
186
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 48 0.051
187
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.051
188
LPT006 Leptin Receptor Deficiency 48 0.051
189
SXL003 Sexual Disorder 47 0.051
190
ACT084 Acute Stress Disorder 47 0.051
191
P CRC039 Coarctation of Aorta 47 0.051
192
RTN020 Retinal Vascular Disease 46 0.051
193
ADR040 Adrenal Gland Pheochromocytoma 46 0.051
194
CRN019 Coronary Artery Vasospasm 46 0.051
195
ANR004 Anuria 46 0.051
196
PST048 Postural Orthostatic Tachycardia Syndrome 45 0.051
197
c HYP272 Hypercholesterolemia, Familial, 3 44 0.051
198
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.051
199
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.051
200
GLC096 Galactorrhea 42 0.051
201
49X006 49, Xxxxy Syndrome 41 0.051
202
VST004 Vestibular Disease 41 0.051
203
RDN001 Reading Disorder 40 0.051
204
PRM020 Premenstrual Tension 40 0.051
205
ENT001 Enterocele 39 0.051
206
FXD003 Fixed Drug Eruption 35 0.051
207
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.051
208
c BNG021 Benign Essential Hypertension 26 0.051
209
P HPT023 Hepatocellular Carcinoma 100 0.036
210
c SYS001 Systemic Lupus Erythematosus 86 0.036
211
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.036
212
P SLP006 Sleep Apnea 69 0.036
213
P HYP086 Hypothyroidism 69 0.036
214
RCK004 Rickets 68 0.036
215
P MJR001 Major Depressive Disorder 68 0.036
216
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.036
217
P DMN002 Dementia 66 0.036
218
KHL003 Kohlschutter-Tonz Syndrome 65 0.036
219
TTN003 Tetanus 65 0.036
220
P ART005 Arteriovenous Malformation 65 0.036
221
P CNJ013 Conjunctivitis 65 0.036
222
KRT019 Keratitis, Hereditary 65 0.036
223
PRT037 Pertussis 65 0.036
224
c DBT099 Diabetes Mellitus, Type I 65 0.036
225
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.036
226
PRT036 Peritonitis 64 0.036
227
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.036
228
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 0.036
229
P HYP069 Hyperparathyroidism 63 0.036
230
TRN015 Transient Cerebral Ischemia 63 0.036
231
DPR016 Depression 63 0.036
232
c GLC092 Glaucoma, Primary Open Angle 62 0.036
233
P PSR002 Psoriasis 62 0.036
234
BLL006 Bullous Pemphigoid 62 0.036
235
DRM006 Dermatitis 61 0.036
236
SZR001 Sezary's Disease 60 0.036
237
P SCL018 Scoliosis 60 0.036
238
VRC005 Varicose Veins 60 0.036
239
c ACT071 Acute Kidney Failure 60 0.036
240
PRT013 Portal Hypertension 59 0.036
241
CHL014 Cholera 59 0.036
242
PLM033 Pulmonary Embolism 59 0.036
243
VSL002 Visual Epilepsy 59 0.036
244
ADN018 Adenoma 59 0.036
245
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.036
246
c LNG047 Long Qt Syndrome 2 58 0.036
247
ERY029 Erythermalgia, Primary 58 0.036
248
PLM070 Pulmonic Stenosis 57 0.036
249
P RHN004 Rhinitis 57 0.036
250
P FCL005 Focal Segmental Glomerulosclerosis 57 0.036
251
VSC002 Vascular Dementia 57 0.036
252
PLC005 Placental Insufficiency 57 0.036
253
PHR003 Pharyngitis 57 0.036
254
P MLT074 Multiple Endocrine Neoplasia 56 0.036
255
c ACT134 Acute Liver Failure 56 0.036
256
P SZR006 Seizure Disorder 56 0.036
257
P PTT006 Pituitary Adenoma 55 0.036
258
OCL020 Ocular Cicatricial Pemphigoid 55 0.036
259
GLC003 Glucose Intolerance 54 0.036
260
PLM010 Pulmonary Edema 54 0.036
261
P ART021 Arteriosclerosis 54 0.036
262
PRS045 Prostatic Hypertrophy 53 0.036
263
INT075 Intracranial Hypertension 53 0.036
264
P PRG013 Paraganglioma 52 0.036
265
PST011 Pustulosis of Palm and Sole 52 0.036
266
PNG002 Pain Agnosia 51 0.036
267
OLG003 Oligohydramnios 51 0.036
268
PRS021 Prostatic Adenoma 51 0.036
269
P LCT001 Lactic Acidosis 51 0.036
270
ESP002 Esophageal Varix 51 0.036
271
PNN001 Panniculitis 51 0.036
272
HYP081 Hypolipoproteinemia 51 0.036
273
P HYP077 Hypertrichosis 50 0.036
274
c SVR005 Severe Pre-Eclampsia 50 0.036
275
PRS129 Prostatic Hyperplasia, Benign 49 0.036
276
47X002 47,xyy 49 0.036
277
P SDR003 Sideroblastic Anemia 49 0.036
278
URM002 Uremia 49 0.036
279
P RNV001 Renovascular Hypertension 48 0.036
280
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.036
281
PRD004 Prediabetes Syndrome 47 0.036
282
CRN017 Coronary Thrombosis 47 0.036
283
RYN005 Raynaud Phenomenon 47 0.036
284
ATN005 Autonomic Dysfunction 46 0.036
285
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.036
286
DST006 Diastolic Heart Failure 45 0.036
287
CRB004 Cerebral Artery Occlusion 45 0.036
288
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.036
289
ATN004 Autonomic Neuropathy 45 0.036
290
c CHR086 Chronic Conjunctivitis 45 0.036
291
DBT090 Diabetes and Deafness, Maternally Inherited 44 0.036
292
CRB008 Cerebral Atherosclerosis 44 0.036
293
PTY001 Pityriasis Rosea 44 0.036
294
FBR019 Fibromatosis 41 0.036
295
PHB001 Phobic Disorder 41 0.036
296
ANX004 Anoxia 40 0.036
297
P PST059 Pustular Psoriasis 37 0.036
298
CRD016 Cardiac Rupture 37 0.036
299
HRT036 Heritable Thoracic Aortic Disease 35 0.036
300
SLN001 Silent Myocardial Infarction 34 0.036
301
EXT054 Extra-Adrenal Pheochromocytoma 34 0.036
302
SBV001 Subvalvular Aortic Stenosis 33 0.036
303
P CRN133 Coronary Artery Disease, Autosomal Dominant, 1 32 0.036
304
INT074 Intracranial Arteriosclerosis 23 0.036
305
AQG001 Aquagenic Pruritus 19 0.036
306
BDR001 Bidirectional Tachycardia 19 0.036
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