Search results for Dobutamine

334 hits were found for Dobutamine

# Family MCID Name MIFTS Score
1
LPP008 Lipoprotein Quantitative Trait Locus 62 0.665
2
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.658
3
ART140 Arteries, Anomalies of 52 0.580
4
CNG034 Congestive Heart Failure 69 0.503
5
CRN030 Coronary Stenosis 50 0.446
6
c ACT075 Acute Myocardial Infarction 57 0.405
7
c DLT002 Dilated Cardiomyopathy 79 0.350
8
c ATR087 Atrial Standstill 1 75 0.341
9
TXC005 Toxic Shock Syndrome 62 0.324
10
ISC004 Ischemia 58 0.313
11
P HRT032 Heart Disease 75 0.311
12
INT007 Intermediate Coronary Syndrome 55 0.297
13
ANG054 Angina Pectoris 66 0.259
14
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.242
15
CRD137 Cardiogenic Shock 47 0.237
16
P CRN300 Coronary Heart Disease 1 63 0.232
17
c MTR002 Mitral Valve Insufficiency 48 0.204
18
PLM010 Pulmonary Edema 54 0.191
19
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.188
20
P MYC007 Myocardial Infarction 70 0.185
21
LFT001 Left Bundle Branch Hemiblock 49 0.178
22
P PLM037 Pulmonary Hypertension 67 0.175
23
MYC005 Myocardial Stunning 46 0.164
24
P KDN018 Kidney Disease 72 0.152
25
P CRD119 Cardiac Arrest 67 0.144
26
P MTR003 Mitral Valve Stenosis 50 0.144
27
SYN036 Syncope 45 0.135
28
48X005 48,xyyy 39 0.135
29
P HYP061 Hypertrophic Cardiomyopathy 70 0.131
30
P TTR001 Tetralogy of Fallot 70 0.131
31
KWS002 Kawasaki Disease 65 0.131
32
ATR057 Atrioventricular Block 55 0.131
33
BRK012 Broken Heart Syndrome 35 0.131
34
LVR012 Liver Cirrhosis 62 0.126
35
P LVR013 Liver Disease 68 0.121
36
c ART101 Aortic Valve Disease 2 65 0.121
37
P VSC007 Vascular Disease 63 0.121
38
END086 End Stage Renal Disease 51 0.121
39
PRP027 Peripheral Vascular Disease 71 0.116
40
P ATR011 Atrial Fibrillation 66 0.116
41
P ADL010 Adult Respiratory Distress Syndrome 65 0.111
42
P CRD246 Cardiovascular System Disease 57 0.111
43
SYS003 Systolic Heart Failure 49 0.111
44
c HYP836 Hypercholesterolemia, Familial, 1 73 0.105
45
CRD132 Cardiac Conduction Defect 58 0.105
46
HYP005 Hypokalemia 55 0.105
47
MTB004 Metabolic Acidosis 50 0.105
48
c PLM022 Pulmonary Valve Insufficiency 39 0.105
49
PLM033 Pulmonary Embolism 59 0.099
50
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 0.099
51
HRT012 Heart Valve Disease 53 0.099
52
HRT011 Heart Septal Defect 50 0.099
53
CRD016 Cardiac Rupture 37 0.099
54
STR067 Stroke, Ischemic 81 0.092
55
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.092
56
LPD008 Lipid Metabolism Disorder 62 0.092
57
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.092
58
HYP266 Hypoxia 57 0.092
59
P ART018 Aortic Valve Insufficiency 49 0.092
60
P RSP003 Respiratory Failure 74 0.086
61
c CHR684 Chronic Kidney Disease 70 0.086
62
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.086
63
ART016 Aortic Aneurysm 69 0.086
64
CRB039 Cerebrovascular Disease 67 0.086
65
c FML001 Familial Atrial Fibrillation 65 0.086
66
PRT036 Peritonitis 64 0.086
67
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.086
68
P MYC008 Myocarditis 59 0.086
69
P TRM003 Tremor 54 0.086
70
PNG002 Pain Agnosia 51 0.086
71
P LCT001 Lactic Acidosis 51 0.086
72
CRN019 Coronary Artery Vasospasm 46 0.086
73
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.086
74
RST023 Resting Heart Rate, Variation in 41 0.086
75
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.078
76
P HYP098 Hypereosinophilic Syndrome 67 0.078
77
ATH013 Atherosclerosis Susceptibility 65 0.078
78
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.078
79
ALL026 Allergic Hypersensitivity Disease 62 0.078
80
P VNT002 Ventricular Septal Defect 60 0.078
81
LNG099 Lung Disease 60 0.078
82
c ACT071 Acute Kidney Failure 60 0.078
83
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.078
84
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.078
85
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 56 0.078
86
47X002 47,xyy 49 0.078
87
BRN071 Brain Injury 49 0.078
88
c TRC022 Tricuspid Valve Insufficiency 45 0.078
89
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.078
90
INF013 Inferior Myocardial Infarction 33 0.078
91
CRR012 Cirrhotic Cardiomyopathy 24 0.078
92
c HYP595 Hypertension, Essential 84 0.070
93
c MCR129 Microvascular Complications of Diabetes 1 66 0.070
94
MSC007 Muscle Hypertrophy 64 0.070
95
P MTR012 Mitral Valve Disease 58 0.070
96
P ART021 Arteriosclerosis 54 0.070
97
INF034 Infective Endocarditis 53 0.070
98
TRM010 Traumatic Brain Injury 51 0.070
99
ATN005 Autonomic Dysfunction 46 0.070
100
CRN020 Coronary Restenosis 39 0.070
101
SCR039 Scorpion Envenomation 38 0.070
102
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.070
103
DBL004 Double Discordia 23 0.070
104
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.061
105
AST005 Asthma 76 0.061
106
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.061
107
P CNR004 Cone-Rod Dystrophy 2 73 0.061
108
ADL002 Adult Syndrome 70 0.061
109
ACR008 Acrocallosal Syndrome 69 0.061
110
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 68 0.061
111
P LNG028 Long Qt Syndrome 66 0.061
112
CHG001 Chagas Disease 66 0.061
113
c MCL013 Mucolipidosis Iv 66 0.061
114
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.061
115
P ORT004 Orthostatic Intolerance 62 0.061
116
NTR005 Nutritional Deficiency Disease 62 0.061
117
HYP066 Hyperglycemia 61 0.061
118
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.061
119
NWB001 Newborn Respiratory Distress Syndrome 58 0.061
120
P END033 Endocarditis 57 0.061
121
AGN016 Aging 56 0.061
122
P SCK002 Sick Sinus Syndrome 55 0.061
123
PRP009 Peripartum Cardiomyopathy 55 0.061
124
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.061
125
HMS001 Hemosiderosis 54 0.061
126
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.061
127
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.061
128
PRV004 Periventricular Leukomalacia 52 0.061
129
P PRC012 Pericardial Effusion 51 0.061
130
PLM041 Pulmonary Valve Stenosis 49 0.061
131
RGH001 Right Bundle Branch Block 48 0.061
132
HMP001 Hemopericardium 48 0.061
133
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.061
134
CRD001 Cardiac Tamponade 47 0.061
135
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.061
136
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.061
137
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.061
138
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.061
139
CYN002 Cyanosis, Transient Neonatal 45 0.061
140
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.061
141
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.061
142
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.061
143
CRB090 Cerebral Hypoxia 44 0.061
144
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.061
145
ATX019 Ataxia with Vitamin E Deficiency 42 0.061
146
P RRH023 Rare Hereditary Hemochromatosis 41 0.061
147
UNV002 Univentricular Heart 28 0.061
148
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.049
149
c BTT014 Beta-Thalassemia 74 0.049
150
MSC157 Muscular Dystrophy, Duchenne Type 72 0.049
151
P PHC003 Pheochromocytoma 71 0.049
152
P AMY004 Amyloidosis 70 0.049
153
CRB037 Cerebral Palsy 69 0.049
154
P SLP006 Sleep Apnea 69 0.049
155
RCK004 Rickets 68 0.049
156
P TRN020 Turner Syndrome 67 0.049
157
OST159 Osteogenic Sarcoma 66 0.049
158
P MSC005 Muscular Dystrophy 66 0.049
159
PPL049 Papillon-Lefevre Syndrome 65 0.049
160
P DBT009 Diabetes Mellitus 64 0.049
161
P HYP069 Hyperparathyroidism 63 0.049
162
c FNC043 Fanconi Anemia, Complementation Group E 62 0.049
163
c HPT003 Hepatitis a 62 0.049
164
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.049
165
P VSC011 Vasculitis 62 0.049
166
P ENC018 Encephalopathy 61 0.049
167
CHR066 Chronic Fatigue Syndrome 61 0.049
168
NTH001 Netherton Syndrome 60 0.049
169
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.049
170
CRD223 Cardiac Arrhythmia 60 0.049
171
P ATR010 Atrial Heart Septal Defect 60 0.049
172
ORL011 Oral Cancer 60 0.049
173
P THL005 Thalassemia 60 0.049
174
PRT013 Portal Hypertension 59 0.049
175
LGS001 Legius Syndrome 59 0.049
176
ANR040 Aneurysm 59 0.049
177
PST028 Post-Traumatic Stress Disorder 58 0.049
178
PLM070 Pulmonic Stenosis 57 0.049
179
P EXN002 Exanthem 57 0.049
180
THR024 Thrombosis 57 0.049
181
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.049
182
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.049
183
INT030 Intracranial Aneurysm 56 0.049
184
c PRG126 Progressive Familial Heart Block 55 0.049
185
AMN003 Amnestic Disorder 54 0.049
186
PRP080 Peripheral Artery Disease 53 0.049
187
c MCR113 Microvascular Complications of Diabetes 3 52 0.049
188
SPS003 Spastic Diplegia 51 0.049
189
OCL069 Ocular Motor Apraxia 51 0.049
190
c SCN007 Secondary Hyperparathyroidism 51 0.049
191
HPT014 Hepatorenal Syndrome 50 0.049
192
SNT005 Sinoatrial Node Disease 49 0.049
193
P RNV001 Renovascular Hypertension 48 0.049
194
ACT084 Acute Stress Disorder 47 0.049
195
c MCR120 Microvascular Complications of Diabetes 7 47 0.049
196
P CRC039 Coarctation of Aorta 47 0.049
197
ADR040 Adrenal Gland Pheochromocytoma 46 0.049
198
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.049
199
SBC016 Subacute Delirium 44 0.049
200
c HYP272 Hypercholesterolemia, Familial, 3 44 0.049
201
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.049
202
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.049
203
CNG134 Congenitally Corrected Transposition of the Great Arteries 41 0.049
204
c MCR130 Microvascular Complications of Diabetes 6 41 0.049
205
c MCR133 Microvascular Complications of Diabetes 4 41 0.049
206
PRS063 Paresthesia 41 0.049
207
RDN001 Reading Disorder 40 0.049
208
ANG049 Angioedema Induced by Ace Inhibitors 40 0.049
209
TRN012 Transient Global Amnesia 39 0.049
210
PRS011 Persian Gulf Syndrome 36 0.049
211
SCN049 Second-Degree Atrioventricular Block 35 0.049
212
P ANT001 Anterolateral Myocardial Infarction 34 0.049
213
c MYC058 Myocardial Infarction 2 34 0.049
214
SNG003 Single Ventricular Heart 30 0.049
215
CHL079 Children's Interstitial Lung Disease 26 0.049
216
P BRS047 Breast Cancer 97 0.035
217
ESP021 Esophageal Cancer 90 0.035
218
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.035
219
c SYS001 Systemic Lupus Erythematosus 86 0.035
220
MYL069 Myeloma, Multiple 85 0.035
221
P BLD134 Bladder Cancer 79 0.035
222
LPT014 Leptin Deficiency or Dysfunction 74 0.035
223
c HMC039 Hemochromatosis, Type 1 74 0.035
224
P HNT016 Huntington Disease 72 0.035
225
ACR007 Acromegaly 71 0.035
226
DFC004 Deficiency Anemia 70 0.035
227
GST040 Gastric Adenocarcinoma 70 0.035
228
P MYP004 Myopathy 70 0.035
229
P OCL013 Oculodentodigital Dysplasia 69 0.035
230
P HYP086 Hypothyroidism 69 0.035
231
P LYM118 Lymphoma 68 0.035
232
P PNM007 Pneumonia 68 0.035
233
P SYS005 Systemic Scleroderma 68 0.035
234
BRN024 Bronchitis 68 0.035
235
P HPT021 Hepatitis 67 0.035
236
c RHB024 Rhabdomyosarcoma 2 67 0.035
237
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.035
238
WLF001 Wolff-Parkinson-White Syndrome 66 0.035
239
HYP056 Hypoglycemia 66 0.035
240
P PLM036 Pulmonary Fibrosis 65 0.035
241
PRT037 Pertussis 65 0.035
242
c DBT099 Diabetes Mellitus, Type I 65 0.035
243
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.035
244
P ADN016 Adenocarcinoma 64 0.035
245
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.035
246
CNT061 Conotruncal Heart Malformations 63 0.035
247
P HYP055 Hypoplastic Left Heart Syndrome 63 0.035
248
TRN015 Transient Cerebral Ischemia 63 0.035
249
DPR016 Depression 63 0.035
250
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.035
251
P PLY014 Polycystic Kidney Disease 62 0.035
252
P ESP024 Esophagitis 62 0.035
253
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.035
254
FTT001 Fatty Liver Disease 61 0.035
255
c PNS012 Paine Syndrome 61 0.035
256
c SCL052 Scleroderma, Familial Progressive 61 0.035
257
P LPS004 Lupus Erythematosus 61 0.035
258
SPN186 Spinal Cord Injury 60 0.035
259
c ACT027 Acute Pancreatitis 60 0.035
260
HPT019 Hepatic Encephalopathy 60 0.035
261
PRT058 Pure Autonomic Failure 59 0.035
262
PRN019 Perinatal Necrotizing Enterocolitis 59 0.035
263
P GLM007 Glomerulonephritis 57 0.035
264
APH002 Aphasia 57 0.035
265
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.035
266
c ACT134 Acute Liver Failure 56 0.035
267
P SZR006 Seizure Disorder 56 0.035
268
BRN004 Brain Edema 56 0.035
269
P PLY019 Polyneuropathy 56 0.035
270
P ATR001 Atrioventricular Septal Defect 55 0.035
271
LMB062 Limb Ischemia 55 0.035
272
ACT058 Active Peptic Ulcer Disease 55 0.035
273
P HYP076 Hyperthyroidism 55 0.035
274
HNC001 Henoch-Schoenlein Purpura 55 0.035
275
HMP005 Hemiplegia 55 0.035
276
PRP030 Purpura 54 0.035
277
PRC013 Pericarditis 54 0.035
278
CLL003 Cellulitis 54 0.035
279
P DDN001 Duodenal Ulcer 52 0.035
280
CRT016 Carotid Artery Disease 52 0.035
281
HYP014 Hyperuricemia 52 0.035
282
ENT011 Enterocolitis 51 0.035
283
LNG031 Lung Benign Neoplasm 51 0.035
284
HYP081 Hypolipoproteinemia 51 0.035
285
CHR005 Chorioamnionitis 51 0.035
286
PTT041 Pituitary Stalk Interruption Syndrome 50 0.035
287
P OVR082 Overgrowth Syndrome 50 0.035
288
c INF145 Infantile Liver Failure Syndrome 1 50 0.035
289
STT002 Status Asthmaticus 50 0.035
290
DYS073 Dysphagia 50 0.035
291
HYP006 Hypertensive Heart Disease 49 0.035
292
URM002 Uremia 49 0.035
293
ASP007 Aspiration Pneumonia 48 0.035
294
LYM019 Lymphosarcoma 46 0.035
295
c ACT076 Acute Myocarditis 46 0.035
296
P MYC033 Myoclonus 46 0.035
297
HDN002 Head Injury 46 0.035
298
HPT004 Hepatic Coma 45 0.035
299
DST006 Diastolic Heart Failure 45 0.035
300
PRT019 Protein-Losing Enteropathy 45 0.035
301
ACT003 Acute Kidney Tubular Necrosis 45 0.035
302
ASP008 Aspiration Pneumonitis 45 0.035
303
CYT002 Cytokine Deficiency 42 0.035
304
ALC010 Alcoholic Cardiomyopathy 42 0.035
305
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.035
306
GST020 Gastric Antral Vascular Ectasia 41 0.035
307
49X006 49, Xxxxy Syndrome 41 0.035
308
CNS002 Constrictive Pericarditis 40 0.035
309
JWD001 Jawad Syndrome 40 0.035
310
CRB086 Cerebral Aneurysms 40 0.035
311
c TRN038 Transposition of the Great Arteries, Dextro-Looped 1 39 0.035
312
CRN006 Coronary Aneurysm 39 0.035
313
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.035
314
MNN021 Meningococcemia 37 0.035
315
PLY161 Polymicrogyria, Bilateral Perisylvian, X-Linked 35 0.035
316
c CNT101 Central Congenital Hypothyroidism 35 0.035
317
c PST106 Post-Cardiac Arrest Syndrome 35 0.035
318
CRN270 Coronary Artery Dissection, Spontaneous 32 0.035
319
HPT085 Hepatitis, Fulminant Viral 32 0.035
320
GST007 Gastric Dilatation 31 0.035
321
ANR010 Aneurysm of Sinus of Valsalva 30 0.035
322
RSP007 Respiratory Distress Syndrome, Infant 30 0.035
323
ART030 Aortic Arch Interruption 29 0.035
324
PST092 Posttransplant Acute Limbic Encephalitis 29 0.035
325
PLS031 Plastic Bronchitis 27 0.035
326
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.035
327
SPL005 Splenic Artery Aneurysm 25 0.035
328
INT053 Intracranial Vasospasm 24 0.035
329
PRP101 Peripheral Pulmonary Stenosis 22 0.035
330
ANT005 Anteroseptal Myocardial Infarction 21 0.035
331
ATR089 Atrioventricular Dissociation 20 0.035
332
SPT001 Septal Myocardial Infarction 18 0.035
333
PLM188 Pulmonary Arterial Hypertension Associated with Another Disease 13 0.035
334
PST002 Posteroinferior Myocardial Infarction 10 0.035
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