Search results for Atenolol

609 hits were found for Atenolol

# Family MCID Name MIFTS Score
1
c HYP595 Hypertension, Essential 84 20.715
2
ANG054 Angina Pectoris 65 11.563
3
RST023 Resting Heart Rate, Variation in 40 6.249
4
MRF001 Marfan Syndrome 76 5.906
5
LPP008 Lipoprotein Quantitative Trait Locus 65 5.843
6
P CRN300 Coronary Heart Disease 1 73 5.170
7
ART140 Arteries, Anomalies of 52 5.019
8
P HMN010 Hemangioma 61 4.790
9
ISC004 Ischemia 61 4.774
10
c ACT075 Acute Myocardial Infarction 55 4.266
11
P VSC007 Vascular Disease 62 4.062
12
P MTR003 Mitral Valve Stenosis 53 3.967
13
MSC007 Muscle Hypertrophy 64 3.848
14
c TYP009 Type 2 Diabetes Mellitus 91 3.709
15
P TRM003 Tremor 50 3.692
16
ATH013 Atherosclerosis Susceptibility 63 3.562
17
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 3.537
18
48X005 48,xyyy 39 3.508
19
ANT039 Antisynthetase Syndrome 55 3.484
20
P ATR011 Atrial Fibrillation 66 3.421
21
c MGR028 Migraine with or Without Aura 1 63 3.419
22
P HRT032 Heart Disease 84 3.413
23
MRD002 Marden-Walker Syndrome 56 3.213
24
HYP540 Hypertension, Diastolic 38 3.112
25
c MCR133 Microvascular Complications of Diabetes 4 41 3.031
26
c MCR113 Microvascular Complications of Diabetes 3 52 3.031
27
c MCR130 Microvascular Complications of Diabetes 6 41 3.031
28
c MCR120 Microvascular Complications of Diabetes 7 47 3.031
29
P FNG006 Feingold Syndrome 1 61 3.029
30
ART016 Aortic Aneurysm 68 2.991
31
c HYP836 Hypercholesterolemia, Familial, 1 73 2.907
32
c PRC016 Pre-Eclampsia 64 2.822
33
HYP005 Hypokalemia 55 2.725
34
CRB039 Cerebrovascular Disease 65 2.722
35
INT007 Intermediate Coronary Syndrome 53 2.688
36
STR067 Stroke, Ischemic 79 2.660
37
P HYP061 Hypertrophic Cardiomyopathy 68 2.653
38
c ATR087 Atrial Standstill 1 74 2.570
39
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.562
40
P HYP750 Hypertriglyceridemia, Familial 61 2.529
41
PRT251 Proteinuria, Chronic Benign 58 2.466
42
CRN030 Coronary Stenosis 50 2.399
43
c MCR115 Microvascular Complications of Diabetes 5 65 2.380
44
P HYP076 Hyperthyroidism 53 2.357
45
HYP056 Hypoglycemia 65 2.345
46
SYN036 Syncope 44 2.334
47
P SCK002 Sick Sinus Syndrome 55 2.322
48
c ART067 Aortic Aneurysm, Familial Thoracic 1 61 2.322
49
CNG034 Congestive Heart Failure 69 2.292
50
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 2.280
51
P ORT004 Orthostatic Intolerance 61 2.273
52
c FML001 Familial Atrial Fibrillation 65 2.272
53
P KDN018 Kidney Disease 71 2.255
54
P CRD246 Cardiovascular System Disease 55 2.236
55
WTH001 Withdrawal Disorder 47 2.196
56
PRP027 Peripheral Vascular Disease 71 2.153
57
END072 Endotheliitis 36 2.126
58
c HYP724 Hyperlipoproteinemia, Type Iii 66 2.114
59
ATR057 Atrioventricular Block 54 2.010
60
IMP005 Impotence 52 2.010
61
CRD223 Cardiac Arrhythmia 63 2.004
62
P MYC007 Myocardial Infarction 69 1.988
63
CPL013 Capillary Malformations, Congenital 53 1.948
64
P ANR048 Aniridia 1 66 1.948
65
P CPL006 Capillary Hemangioma 53 1.948
66
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 1.941
67
ALL029 Allergic Disease 61 1.935
68
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.911
69
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 1.911
70
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.911
71
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 1.911
72
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.911
73
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 1.911
74
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 1.911
75
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.911
76
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.911
77
P EXN002 Exanthem 58 1.856
78
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 1.852
79
c HNT004 Huntington Disease-Like 2 51 1.846
80
P DBT009 Diabetes Mellitus 67 1.833
81
CYT002 Cytokine Deficiency 43 1.833
82
ANR040 Aneurysm 60 1.829
83
RTR011 Retroperitoneal Fibrosis 47 1.825
84
ART074 Aortic Dissection 53 1.814
85
P ECL001 Eclampsia 52 1.811
86
P FML187 Familial Hypertension 34 1.802
87
SCL003 Social Phobia 48 1.791
88
P CRD119 Cardiac Arrest 68 1.783
89
LPD008 Lipid Metabolism Disorder 61 1.783
90
OCL006 Ocular Hypertension 53 1.780
91
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 1.717
92
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 1.717
93
c BLD140 Blood Group, I System 47 1.717
94
CRB009 Cerebritis 43 1.717
95
END086 End Stage Renal Disease 54 1.704
96
c DLT002 Dilated Cardiomyopathy 79 1.693
97
CRD132 Cardiac Conduction Defect 59 1.675
98
P HDC001 Headache 56 1.660
99
P PHC003 Pheochromocytoma 70 1.646
100
ADR040 Adrenal Gland Pheochromocytoma 45 1.646
101
c HNT011 Huntington Disease-Like 3 33 1.612
102
HYP066 Hyperglycemia 60 1.566
103
MTR002 Mitral Valve Insufficiency 51 1.559
104
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 33 1.531
105
P LNG028 Long Qt Syndrome 63 1.529
106
RHB024 Rhabdomyosarcoma 2 65 1.516
107
ATX019 Ataxia with Vitamin E Deficiency 44 1.516
108
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 1.516
110
P FML364 Familial Thoracic Aortic Aneurysm and Aortic Dissection 70 1.516
111
c ESS001 Essential Tremor 56 1.511
112
P OPN001 Open-Angle Glaucoma 55 1.499
113
INT002 Intermittent Claudication 61 1.463
114
SXL003 Sexual Disorder 49 1.439
115
ANX010 Anxiety 70 1.410
116
P DRR001 Diarrhea 55 1.410
117
STT001 Status Epilepticus 58 1.410
118
c GRV008 Graves Disease 1 54 1.389
119
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.350
120
P ART018 Aortic Valve Insufficiency 52 1.350
121
BRN024 Bronchitis 67 1.334
122
PRT058 Pure Autonomic Failure 58 1.323
123
CRD137 Cardiogenic Shock 56 1.316
124
PLM129 Pulmonary Disease, Chronic Obstructive 74 1.293
125
CNS004 Constipation 56 1.261
126
DST006 Diastolic Heart Failure 45 1.252
127
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 1.180
128
c BNG021 Benign Essential Hypertension 37 1.174
129
P CRC039 Coarctation of Aorta 46 1.157
130
P VSC011 Vasculitis 61 1.157
131
ADL002 Adult Syndrome 69 1.157
132
CRN019 Coronary Artery Vasospasm 47 1.140
133
PRM020 Premenstrual Tension 39 1.140
134
RTN020 Retinal Vascular Disease 45 1.122
135
ANR004 Anuria 44 1.122
136
P RNL015 Renal Hypertension 45 1.122
137
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.103
138
GLC096 Galactorrhea 40 1.082
139
HYP020 Hyperprolactinemia 63 1.082
140
LNG099 Lung Disease 62 1.082
141
RYN005 Raynaud Phenomenon 45 1.081
142
c LNG047 Long Qt Syndrome 2 59 1.069
143
ATN005 Autonomic Dysfunction 45 1.069
144
DFC004 Deficiency Anemia 74 1.068
145
c ART115 Aortic Valve Disease 1 72 1.068
146
PST048 Postural Orthostatic Tachycardia Syndrome 46 1.068
147
FXD003 Fixed Drug Eruption 34 1.060
148
P SLP006 Sleep Apnea 69 1.057
149
TRN015 Transient Cerebral Ischemia 62 1.057
150
PRT037 Pertussis 49 1.044
151
CRD016 Cardiac Rupture 34 1.044
152
VST004 Vestibular Disease 40 1.044
153
CHL068 Cholestasis 61 1.036
154
P RNV001 Renovascular Hypertension 48 1.004
155
PRT013 Portal Hypertension 59 0.990
156
SNT005 Sinoatrial Node Disease 48 0.980
157
ART017 Aortic Disease 49 0.980
158
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.975
159
LVR012 Liver Cirrhosis 62 0.975
160
VRC005 Varicose Veins 59 0.960
161
PLM010 Pulmonary Edema 54 0.960
162
PRT036 Peritonitis 65 0.960
163
47X002 47,xyy 47 0.960
164
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.956
165
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 0.956
166
P OST002 Osteoporosis 76 0.956
167
c HYP272 Hypercholesterolemia, Familial, 3 46 0.956
168
P MCR129 Microvascular Complications of Diabetes 1 67 0.956
169
AGN016 Aging 53 0.956
170
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.956
171
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.956
172
c MCR112 Microvascular Complications of Diabetes 2 42 0.956
173
c ART101 Aortic Valve Disease 2 65 0.956
174
LPT014 Leptin Deficiency or Dysfunction 77 0.956
175
LPT006 Leptin Receptor Deficiency 50 0.956
176
HYP555 Hypertriglyceridemia, Transient Infantile 39 0.956
177
PST028 Post-Traumatic Stress Disorder 58 0.956
178
ACT084 Acute Stress Disorder 53 0.956
179
AND005 Androgen Insensitivity Syndrome, Mild 21 0.956
180
KRT001 Keratoconjunctivitis Sicca 49 0.944
181
KRT006 Keratoconjunctivitis 53 0.944
182
c SVR005 Severe Pre-Eclampsia 49 0.944
183
P LCT001 Lactic Acidosis 50 0.944
184
P SZR006 Seizure Disorder 69 0.927
185
c DWL002 Dowling-Degos Disease 1 58 0.910
186
P RHN004 Rhinitis 56 0.910
187
TLN003 Telangiectasis 51 0.910
188
OCL069 Ocular Motor Apraxia 57 0.892
189
PHR003 Pharyngitis 57 0.892
190
P HYP086 Hypothyroidism 68 0.892
191
CRB004 Cerebral Artery Occlusion 45 0.892
192
INT075 Intracranial Hypertension 52 0.892
193
PRS129 Prostatic Hyperplasia, Benign 48 0.872
194
ESP002 Esophageal Varix 51 0.872
195
PRS021 Prostatic Adenoma 43 0.872
196
PRS045 Prostatic Hypertrophy 53 0.872
197
P FCL005 Focal Segmental Glomerulosclerosis 57 0.872
198
c MLG069 Malignant Hypertension 46 0.872
199
FML035 Familial Hyperlipidemia 54 0.852
200
PMP014 Pemphigoid 48 0.852
201
BLL006 Bullous Pemphigoid 61 0.852
202
P NRP001 Neuropathy 59 0.852
203
P SCL018 Scoliosis 57 0.830
204
PLM070 Pulmonic Stenosis 49 0.830
205
P MJR001 Major Depressive Disorder 68 0.830
206
c ACT071 Acute Kidney Failure 60 0.830
207
P ALC033 Alcohol Use Disorder 67 0.830
208
CNN005 Connective Tissue Disease 66 0.830
209
URM002 Uremia 47 0.830
210
ATN004 Autonomic Neuropathy 42 0.830
211
CRN017 Coronary Thrombosis 46 0.830
212
SLN001 Silent Myocardial Infarction 33 0.830
213
SBV001 Subvalvular Aortic Stenosis 31 0.830
214
c ACT134 Acute Liver Failure 57 0.830
215
c SYS001 Systemic Lupus Erythematosus 85 0.806
216
PLC005 Placental Insufficiency 55 0.806
217
CHL014 Cholera 62 0.806
218
P LPS004 Lupus Erythematosus 61 0.806
219
FBR019 Fibromatosis 44 0.806
220
ANX004 Anoxia 40 0.806
221
IRR002 Irritable Bowel Syndrome 64 0.785
222
ERY029 Erythermalgia, Primary 57 0.780
223
P PNC035 Pancreatic Cancer 87 0.780
224
c TYP008 Type 1 Diabetes Mellitus 77 0.780
225
ADN018 Adenoma 58 0.780
226
PST011 Pustulosis of Palm and Sole 52 0.780
227
P PTT006 Pituitary Adenoma 55 0.780
228
P ADL010 Adult Respiratory Distress Syndrome 70 0.780
229
OLG003 Oligohydramnios 50 0.780
230
AQG001 Aquagenic Pruritus 18 0.780
231
P PSR002 Psoriasis 63 0.780
232
PTY001 Pityriasis Rosea 44 0.780
233
HRT036 Heritable Thoracic Aortic Disease 36 0.780
234
P PRG013 Paraganglioma 57 0.750
235
c GLC092 Glaucoma, Primary Open Angle 60 0.750
236
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.750
237
P CNJ013 Conjunctivitis 66 0.750
238
PNN001 Panniculitis 52 0.750
239
P PST059 Pustular Psoriasis 37 0.750
240
c CHR684 Chronic Kidney Disease 73 0.747
241
DBT090 Diabetes and Deafness, Maternally Inherited 44 0.714
242
BCH004 Bachmann-Bupp Syndrome 31 0.714
243
KRT019 Keratitis, Hereditary 66 0.714
244
P RSP003 Respiratory Failure 73 0.714
245
P HYP069 Hyperparathyroidism 62 0.714
246
c CHR086 Chronic Conjunctivitis 42 0.714
247
EXT054 Extra-Adrenal Pheochromocytoma 31 0.714
248
PHB001 Phobic Disorder 45 0.714
249
SBC016 Subacute Delirium 42 0.714
250
P ART021 Arteriosclerosis 53 0.696
251
P ANG015 Angioedema 56 0.696
252
P PRC031 Preeclampsia/eclampsia 1 43 0.684
253
P HYP077 Hypertrichosis 48 0.668
254
P ART005 Arteriovenous Malformation 64 0.668
255
P SDR003 Sideroblastic Anemia 49 0.668
256
SZR001 Sezary's Disease 60 0.668
257
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 64 0.631
258
GLC003 Glucose Intolerance 53 0.584
259
c CHR711 Chronic Asthma 41 0.555
260
PLC008 Placenta Disease 48 0.484
261
C1N001 C1 Inhibitor Deficiency 43 0.472
262
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 0.472
263
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 65 0.472
264
ATX049 Ataxia with Vitamin 3 Deficiency 52 0.472
265
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 52 0.472
266
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.472
268
NTR005 Nutritional Deficiency Disease 60 0.472
269
PRD004 Prediabetes Syndrome 52 0.472
270
RCK004 Rickets 64 0.472
271
KRT002 Keratomalacia 54 0.472
272
CVD001 Covid-19 59 0.472
273
HNT002 Hantavirus Pulmonary Syndrome 55 0.472
274
INT074 Intracranial Arteriosclerosis 23 0.472
275
CRB008 Cerebral Atherosclerosis 45 0.472
276
CTS005 Catastrophic Antiphospholipid Syndrome 43 0.472
277
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.472
278
P GLM007 Glomerulonephritis 59 0.448
279
HYP006 Hypertensive Heart Disease 48 0.388
280
MYC005 Myocardial Stunning 45 0.388
281
c PRG042 Progressive Familial Heart Block, Type Ia 65 0.372
282
HYP060 Hyperinsulinism 53 0.372
283
HDN002 Head Injury 44 0.372
284
HRT012 Heart Valve Disease 53 0.354
285
BNR002 Bone Resorption Disease 47 0.336
286
P GRV001 Graves' Disease 54 0.336
287
RYN001 Raynaud Disease 49 0.317
288
HYP014 Hyperuricemia 51 0.317
289
GTR002 Goiter 52 0.317
290
P MYC008 Myocarditis 59 0.317
291
c FML191 Familial Long Qt Syndrome 54 0.317
292
RNL077 Renal Fibrosis 46 0.297
293
APN008 Apnea, Obstructive Sleep 66 0.297
294
NPH010 Nephrosclerosis 50 0.297
295
HYP114 Hypertensive Nephropathy 35 0.275
296
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.275
297
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.275
298
AMN003 Amnestic Disorder 53 0.275
299
P PRD008 Periodontitis 63 0.275
300
SYS003 Systolic Heart Failure 49 0.275
301
P SCL048 Sclerosteosis 58 0.251
302
MTB004 Metabolic Acidosis 48 0.251
303
PPL052 Papillomatosis, Confluent and Reticulated 34 0.251
304
c LNG048 Long Qt Syndrome 3 52 0.251
305
P PLM037 Pulmonary Hypertension 69 0.251
306
P AST005 Asthma 75 0.251
307
P PLY014 Polycystic Kidney Disease 71 0.251
308
CLN015 Colon Adenocarcinoma 64 0.251
309
P NTR004 Neutropenia 62 0.251
310
PLM041 Pulmonary Valve Stenosis 50 0.251
311
SKN016 Skin Disease 63 0.251
312
PPT005 Peptic Ulcer Disease 58 0.251
313
P NRB001 Neuroblastoma 66 0.251
314
GST050 Gastrointestinal System Disease 55 0.251
315
DYS073 Dysphagia 53 0.251
316
PRS063 Paresthesia 39 0.251
317
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.224
318
FRS012 First-Degree Atrioventricular Block 39 0.224
319
CYS001 Cystic Fibrosis 77 0.224
320
P PRS040 Prostate Cancer 95 0.224
321
c NPH055 Nephrotic Syndrome, Type 1 52 0.224
323
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.224
324
LWC001 Low Compliance Bladder 44 0.224
325
RHM001 Rheumatic Fever 59 0.224
326
MNT002 Mental Depression 56 0.224
327
LFT001 Left Bundle Branch Hemiblock 47 0.224
328
GT001 Gout 63 0.224
329
PLC007 Placental Abruption 47 0.224
330
GRN017 Granulocytopenia 42 0.224
331
P THY054 Thyrotoxic Periodic Paralysis 51 0.224
332
BRN071 Brain Injury 50 0.224
333
P PRD021 Periodic Paralysis 42 0.224
335
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.194
336
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 44 0.194
337
PNG002 Pain Agnosia 51 0.194
338
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 0.194
339
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 0.194
340
EPD052 Epidermolysis Bullosa Simplex Superficialis 17 0.194
341
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.194
342
P GLM040 Glioma Susceptibility 1 70 0.194
343
P NPH012 Nephrotic Syndrome 61 0.194
344
MLG169 Malignant Astrocytoma 57 0.194
345
NRT004 Neuritis 53 0.194
346
HRT011 Heart Septal Defect 49 0.194
347
P PRP019 Peripheral Nervous System Disease 57 0.194
348
P MYP004 Myopathy 67 0.194
349
GNG012 Gingival Overgrowth 49 0.194
350
TTN003 Tetanus 64 0.194
351
RGH001 Right Bundle Branch Block 47 0.194
352
c ATS347 Autosomal Dominant Polycystic Kidney Disease 64 0.194
353
P LPC002 Lip Cancer 46 0.194
354
ACT058 Active Peptic Ulcer Disease 55 0.194
355
P HYP120 Hypoaldosteronism 33 0.194
356
P HYP098 Hypereosinophilic Syndrome 66 0.194
357
RFR010 Refractory Anemia 49 0.194
358
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.194
359
P OVR082 Overgrowth Syndrome 41 0.194
360
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 0.159
361
c LNG044 Long Qt Syndrome 1 66 0.159
362
ATR089 Atrioventricular Dissociation 21 0.159
363
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.159
364
ALC007 Alcohol Dependence 65 0.159
365
c PRD040 Periodontitis, Chronic 52 0.159
366
INS024 Insulin-Like Growth Factor I 77 0.159
367
P BRS047 Breast Cancer 97 0.159
368
P MLT020 Multiple Sclerosis 79 0.159
369
P DRM053 Dermatitis, Atopic 65 0.159
370
TRD006 Tardive Dyskinesia 53 0.159
371
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.159
372
LNG105 Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome 36 0.159
373
ANR007 Anorexia Nervosa 59 0.159
374
P BRG001 Brugada Syndrome 69 0.159
375
WLF001 Wolff-Parkinson-White Syndrome 63 0.159
376
P MYS003 Myasthenia Gravis 67 0.159
377
SDD001 Sudden Infant Death Syndrome 60 0.159
378
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.159
379
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.159
380
THY069 Thyroid Hormone Resistance, Selective Pituitary 36 0.159
381
P LNG064 Lung Cancer Susceptibility 3 69 0.159
382
PNC085 Penicillin Allergy 43 0.159
383
OST017 Osteomyelitis 63 0.159
384
HYP008 Hypertensive Retinopathy 39 0.159
385
INT067 Interstitial Nephritis 46 0.159
386
INT030 Intracranial Aneurysm 55 0.159
387
c ATM011 Autoimmune Hepatitis 62 0.159
388
P ATR010 Atrial Heart Septal Defect 58 0.159
389
P MLN007 Male Infertility 56 0.159
390
P MVM001 Movement Disease 61 0.159
391
BRN004 Brain Edema 54 0.159
392
ART008 Arteriosclerosis Obliterans 40 0.159
393
SCH012 Schizoaffective Disorder 49 0.159
394
AMN001 Amenorrhea 53 0.159
395
c VRL010 Viral Hepatitis 52 0.159
396
P ANT006 Antiphospholipid Syndrome 55 0.159
397
P ADN016 Adenocarcinoma 63 0.159
398
P LVR013 Liver Disease 68 0.159
399
P SKN015 Skin Carcinoma 71 0.159
400
TNS005 Tonsillitis 57 0.159
401
P THR014 Thrombocytopenia 66 0.159
402
P INF032 Infertility 60 0.159
403
P RTN018 Retinal Disease 53 0.159
404
P HML002 Hemolytic Anemia 62 0.159
405
P PNC025 Panic Disorder 52 0.159
406
P NRF002 Neurofibromatosis 60 0.159
407
RSC001 Rosacea 55 0.159
408
P NRC002 Narcolepsy 55 0.159
409
OST012 Osteoarthritis 77 0.159
410
c SBC007 Subacute Thyroiditis 43 0.159
411
P THY032 Thyroiditis 56 0.159
412
THR123 Thrombotic Microangiopathy 40 0.159
413
ADG002 Audiogenic Seizures 25 0.159
414
P ENC018 Encephalopathy 62 0.159
415
SPN186 Spinal Cord Injury 60 0.159
416
c MJR022 Major Affective Disorder 8 37 0.112
417
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.112
418
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.112
419
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.112
420
PRP001 Propionic Acidemia 65 0.112
421
P PTS002 Ptosis 52 0.112
422
UVL006 Uvulitis 23 0.112
423
BLR027 Blue Rubber Bleb Nevus 39 0.112
424
c VSC019 Vesicoureteral Reflux 1 56 0.112
425
LPD012 Lipoid Congenital Adrenal Hyperplasia 68 0.112
426
CRB160 Cerebellar Ataxia, Early-Onset, with Retained Tendon Reflexes 26 0.112
427
c ANM038 Anemia, Autoimmune Hemolytic 63 0.112
428
P NNN008 Noonan Syndrome 1 76 0.112
429
OBS002 Obsessive-Compulsive Disorder 67 0.112
430
c MLT160 Multiple Endocrine Neoplasia, Type Iia 67 0.112
431
LYM133 Lymphoma, Hodgkin, Classic 69 0.112
432
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.112
433
CRN270 Coronary Artery Dissection, Spontaneous 33 0.112
434
P CLR023 Colorectal Cancer 100 0.112
436
c RTN047 Retinitis Pigmentosa 18 45 0.112
437
P PTN014 Patent Ductus Arteriosus 1 59 0.112
438
HYP017 Hypophosphatemia 49 0.112
439
P FML011 Familial Adenomatous Polyposis 70 0.112
440
P FML012 Familial Partial Lipodystrophy 54 0.112
441
c HPT073 Hepatitis C Virus 70 0.112
442
c MJR024 Major Affective Disorder 9 40 0.112
443
P GST053 Gastric Cancer 82 0.112
444
IFP003 Ifap Syndrome 2 41 0.112
445
CYN002 Cyanosis, Transient Neonatal 43 0.112
446
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.112
447
ANG020 Angiosarcoma 63 0.112
448
ANG049 Angioedema Induced by Ace Inhibitors 38 0.112
449
ADR052 Adrenal Hyperplasia, Congenital, Due to 17-Alpha-Hydroxylase Deficiency 44 0.112
450
ENT011 Enterocolitis 55 0.112
451
CNT105 Central Core Disease of Muscle 59 0.112
452
P TTR001 Tetralogy of Fallot 69 0.112
453
P TRT019 Torticollis 47 0.112
454
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.112
455
MYL069 Myeloma, Multiple 76 0.112
456
c PSR021 Psoriasis 14, Pustular 57 0.112
457
P GRF003 Graft-Versus-Host Disease 71 0.112
458
P MMB011 Membranous Nephropathy 50 0.112
459
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.112
460
MCN017 Meconium Ileus 52 0.112
461
KWS002 Kawasaki Disease 65 0.112
462
PRP009 Peripartum Cardiomyopathy 54 0.112
463
ARC023 Arcus Corneae 36 0.112
464
ATM095 Autoimmune Disease 61 0.112
465
CRT072 Creutzfeldt-Jakob Disease 67 0.112
466
ESP021 Esophageal Cancer 84 0.112
467
HRW001 Hair Whorl 35 0.112
468
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.112
469
HMN044 Human Immunodeficiency Virus Type 1 76 0.112
470
P FTL002 Fatal Familial Insomnia 50 0.112
471
OVR029 Ovarian Hyperstimulation Syndrome 63 0.112
472
KRN002 Kearns-Sayre Syndrome 62 0.112
473
P MLT008 Multinodular Goiter 41 0.112
474
P MYG005 Myoglobinuria 40 0.112
475
P PRK039 Parkinsonism 55 0.112
476
TCL003 T Cell Deficiency 44 0.112
477
DSS009 Disseminated Intravascular Coagulation 56 0.112
478
NNL006 Non-Alcoholic Steatohepatitis 54 0.112
479
PRP080 Peripheral Artery Disease 54 0.112
480
CLR109 Colorectal Adenocarcinoma 50 0.112
481
MNN032 Meningococcal Meningitis 52 0.112
482
BLP004 Blepharophimosis 36 0.112
483
GST023 Gastric Ulcer 52 0.112
484
P VNT002 Ventricular Septal Defect 58 0.112
485
P CYS018 Cystitis 58 0.112
486
PTN001 Patent Foramen Ovale 61 0.112
487
P CRN037 Craniosynostosis 67 0.112
488
HYP080 Hypogonadism 49 0.112
489
P THR015 Thrombophilia 51 0.112
490
c BSL007 Basal Cell Carcinoma 67 0.112
491
SQM006 Squamous Cell Carcinoma 59 0.112
492
CHL067 Cholecystitis 59 0.112
493
HMS001 Hemosiderosis 48 0.112
494
P ISL078 Isolated Ectopia Lentis 58 0.112
495
HMP001 Hemopericardium 47 0.112
496
MSN001 Mesangial Proliferative Glomerulonephritis 44 0.112
497
P TRN020 Turner Syndrome 67 0.112
498
P EYD002 Eye Disease 57 0.112
499
CRN020 Coronary Restenosis 39 0.112
500
AKN002 Akinetic Mutism 36 0.112
501
P MLT074 Multiple Endocrine Neoplasia 58 0.112
502
P BPL003 Bipolar Disorder 56 0.112
503
PRP016 Paraplegia 52 0.112
504
SVR004 Severe Combined Immunodeficiency 70 0.112
505
P ANT001 Anterolateral Myocardial Infarction 34 0.112
506
INF013 Inferior Myocardial Infarction 33 0.112
507
INT042 Internuclear Ophthalmoplegia 32 0.112
508
P HPT021 Hepatitis 68 0.112
509
GST045 Gastroenteritis 58 0.112
510
PLM022 Pulmonary Valve Insufficiency 45 0.112
511
RYS001 Reye Syndrome 49 0.112
512
PPL021 Papilledema 49 0.112
513
P PLY011 Polycystic Ovary Syndrome 57 0.112
514
BRN038 Bronchial Disease 51 0.112
515
c HPT001 Hepatitis C 61 0.112
516
P END033 Endocarditis 58 0.112
517
IGG001 Iga Glomerulonephritis 50 0.112
518
MRP001 Morphine Dependence 41 0.112
519
P KDN017 Kidney Cancer 60 0.112
520
DRM006 Dermatitis 61 0.112
521
TRC022 Tricuspid Valve Insufficiency 46 0.112
522
P SYP003 Syphilis 59 0.112
523
MTS001 Mutism 44 0.112
524
TST015 Testicular Disease 42 0.112
525
HGH043 High Grade Glioma 46 0.112
526
c ACT076 Acute Myocarditis 46 0.112
527
c SCN007 Secondary Hyperparathyroidism 50 0.112
528
P BRS044 Breast Adenocarcinoma 58 0.112
529
P PSD003 Pseudohypoaldosteronism 45 0.112
530
P PRL003 Proliferative Glomerulonephritis 43 0.112
531
P SBS003 Substance Abuse 54 0.112
532
CNN003 Conn's Syndrome 77 0.112
533
PRT018 Portal Vein Thrombosis 50 0.112
534
P PRC012 Pericardial Effusion 50 0.112
535
P HYP040 Hypospadias 51 0.112
536
c ACT068 Acute Cystitis 60 0.112
537
TXC004 Toxic Diffuse Goiter 24 0.112
538
BRD004 Borderline Personality Disorder 53 0.112
539
PLM011 Plummer's Disease 34 0.112
540
LNS001 Lens Subluxation 40 0.112
541
P MGR001 Migraine Without Aura 48 0.112
542
INT394 Intermittent Asthma 21 0.112
543
CHG001 Chagas Disease 65 0.112
544
TXC005 Toxic Shock Syndrome 61 0.112
545
GNR004 Generalized Anxiety Disorder 54 0.112
546
P GND004 Gonadal Dysgenesis 46 0.112
547
DMP001 Dumping Syndrome 43 0.112
548
P PRS038 Personality Disorder 65 0.112
549
P URT039 Urticaria 57 0.112
550
VRT003 Vertebrobasilar Insufficiency 31 0.112
551
NDL007 Nodular Goiter 48 0.112
552
HYD002 Hydronephrosis 58 0.112
553
PRN009 Paranoid Schizophrenia 49 0.112
554
P INT070 Intestinal Obstruction 57 0.112
555
P SLP005 Sleep Disorder 61 0.112
556
P PRN023 Prion Disease 60 0.112
557
GST040 Gastric Adenocarcinoma 66 0.112
558
ILS001 Ileus 49 0.112
559
ALL006 Allergic Asthma 55 0.112
560
LRN003 Learning Disability 49 0.112
561
HYP057 Hypervitaminosis D 37 0.112
562
SCT002 Scotoma 42 0.112
563
HYP034 Hypertensive Encephalopathy 43 0.112
564
P BRN022 Bronchiectasis 59 0.112
565
DYS011 Dyskinesia of Esophagus 41 0.112
566
P LCH002 Lichen Planus 54 0.112
567
PRP005 Parapsoriasis 38 0.112
568
P MLG056 Malignant Hyperthermia 65 0.112
569
ULC004 Ulcerative Colitis 74 0.112
570
APP008 Appendicitis 62 0.112
571
PYR009 Pyridoxine Deficiency Anemia 35 0.112
572
CHR066 Chronic Fatigue Syndrome 59 0.112
573
PLY012 Polyhydramnios 46 0.112
574
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.112
575
P CRN074 Coronary Artery Aneurysm 41 0.112
576
GLM045 Glioma 62 0.112
577
MLT037 Multifocal Lymphangioendotheliomatosis with Thrombocytopenia 17 0.112
578
PRN019 Perinatal Necrotizing Enterocolitis 60 0.112
579
VSC002 Vascular Dementia 59 0.112
580
ALL014 Allergic Encephalomyelitis 34 0.112
581
BRK012 Broken Heart Syndrome 42 0.112
582
P AMY004 Amyloidosis 69 0.112
583
P SBR004 Seborrheic Dermatitis 44 0.112
584
EXP004 Exophthalmos 50 0.112
585
ANG037 Angiomatosis 31 0.112
586
CHR178 Chromosomal Triplication 33 0.112
587
DXR001 Doxorubicin Induced Cardiomyopathy 32 0.112
588
c ALM001 Al Amyloidosis 54 0.112
589
TRM010 Traumatic Brain Injury 50 0.112
590
P RRH023 Rare Hereditary Hemochromatosis 52 0.112
591
ACT167 Acute Generalized Exanthematous Pustulosis 38 0.112
592
PLY100 Polyploidy 36 0.112
593
c PSD047 Pseudo-Turner Syndrome 52 0.112
594
PYR016 Pyridoxine Deficiency 29 0.112
595
BNG077 Benign Idiopathic Neonatal Seizures 23 0.112
596
SRT004 Serotonin Syndrome 54 0.112
597
PRN071 Parenteral Nutrition-Associated Cholestasis 23 0.112
598
DSC009 Discoid Lupus Erythematosus 42 0.112
599
c CHR417 Chronic Graft Versus Host Disease 55 0.112
600
DWR001 Dwarfism 44 0.112
601
MST020 Mast Cell Activation Syndrome 27 0.112
602
P MYC033 Myoclonus 46 0.112
603
c UNP011 Uniparental Disomy of Chromosome 14 15 0.112
604
PRM050 Primary Orthostatic Tremor 24 0.112
605
DPR016 Depression 64 0.112
606
P DYS021 Dysautonomia 38 0.112
607
GLL048 Glial Tumor 51 0.112
608
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 0.112
609
PRM329 Premature Aging 36 0.112
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