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Search results for Milrinone

306 hits were found for Milrinone

# Family MCID Name MIFTS Score
1
P PLM037 Pulmonary Hypertension 72 21.064
2
CNG034 Congestive Heart Failure 69 14.680
3
P HRT032 Heart Disease 81 11.346
4
CRD137 Cardiogenic Shock 56 8.850
5
TXC005 Toxic Shock Syndrome 62 8.350
6
ISC004 Ischemia 61 7.669
7
PLM010 Pulmonary Edema 55 7.143
8
MTR002 Mitral Valve Insufficiency 52 6.956
9
P THR014 Thrombocytopenia 66 6.901
10
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 6.770
11
c ATR087 Atrial Standstill 1 74 6.735
12
c DLT002 Dilated Cardiomyopathy 78 6.566
13
P VNT002 Ventricular Septal Defect 58 6.391
14
c DPH024 Diaphragmatic Hernia, Congenital 64 5.776
15
P RSP003 Respiratory Failure 74 5.776
16
HRT011 Heart Septal Defect 49 5.730
17
48X005 48,xyyy 39 5.576
18
LPP008 Lipoprotein Quantitative Trait Locus 65 5.082
19
c ACT075 Acute Myocardial Infarction 56 5.055
20
P PTN014 Patent Ductus Arteriosus 1 59 4.828
21
MYC005 Myocardial Stunning 46 4.747
22
c ACT071 Acute Kidney Failure 60 4.613
23
P MYC007 Myocardial Infarction 70 4.490
24
P VSC007 Vascular Disease 63 4.487
25
STR067 Stroke, Ischemic 80 4.409
26
ART140 Arteries, Anomalies of 53 4.407
27
P TTR001 Tetralogy of Fallot 69 4.319
28
c HYP595 Hypertension, Essential 85 4.270
29
P KDN018 Kidney Disease 72 4.074
30
HYP005 Hypokalemia 55 4.028
31
CRD132 Cardiac Conduction Defect 60 3.842
32
P CRD119 Cardiac Arrest 67 3.791
33
c PLM164 Pulmonary Hypertension, Primary, 1 76 3.780
34
HYP266 Hypoxia 57 3.680
35
MTH009 Mouth Disease 57 3.588
36
HND002 Hand, Foot and Mouth Disease 50 3.488
37
PRT037 Pertussis 65 3.480
38
SNG003 Single Ventricular Heart 30 3.437
39
P MTR003 Mitral Valve Stenosis 53 3.385
40
SYS003 Systolic Heart Failure 49 3.338
41
ANT039 Antisynthetase Syndrome 55 3.236
42
c CHR684 Chronic Kidney Disease 69 3.106
43
ANG054 Angina Pectoris 66 3.047
44
RVR002 Reversible Cerebral Vasoconstriction Syndrome 28 2.865
45
INT002 Intermittent Claudication 61 2.856
46
CRT084 Creatinine Clearance Quantitative Trait Locus 25 2.787
47
P ATR011 Atrial Fibrillation 66 2.717
48
P ENC004 Encephalitis 61 2.717
49
TRC022 Tricuspid Valve Insufficiency 47 2.694
50
P BLD124 Bleeding Disorder, Platelet-Type, 11 67 2.694
51
P CRN300 Coronary Heart Disease 1 73 2.686
52
ANR040 Aneurysm 61 2.686
53
P HYD006 Hydrocephalus 61 2.644
54
IMP005 Impotence 52 2.633
55
P URN019 Urinary Tract Infection 49 2.605
56
P ADL010 Adult Respiratory Distress Syndrome 71 2.605
57
DST006 Diastolic Heart Failure 45 2.600
58
BNR002 Bone Resorption Disease 47 2.467
59
P HYP055 Hypoplastic Left Heart Syndrome 65 2.467
60
CYT002 Cytokine Deficiency 43 2.467
61
P ART018 Aortic Valve Insufficiency 52 2.404
62
P HYP076 Hyperthyroidism 53 2.404
63
CMP035 Complete Atrioventricular Canal 24 2.404
64
c ART101 Aortic Valve Disease 2 66 2.366
65
CRB009 Cerebritis 43 2.357
66
P DXT004 Dextro-Looped Transposition of the Great Arteries 58 2.317
67
P ATR001 Atrioventricular Septal Defect 55 2.316
68
ART016 Aortic Aneurysm 68 2.316
69
MSC157 Muscular Dystrophy, Duchenne Type 79 2.238
70
PRP027 Peripheral Vascular Disease 71 2.238
71
OCL069 Ocular Motor Apraxia 57 2.238
72
P MSC005 Muscular Dystrophy 67 2.238
73
INT030 Intracranial Aneurysm 55 2.208
74
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.169
75
P INT260 Intracranial Berry Aneurysm 40 2.169
76
ALV007 Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins 48 2.169
77
c HYP724 Hyperlipoproteinemia, Type Iii 67 2.169
78
PRS030 Persistent Fetal Circulation Syndrome 49 2.169
79
SYN036 Syncope 45 2.154
80
HRP001 Herpangina 43 2.154
81
P MYC008 Myocarditis 59 2.129
82
CRT015 Carotid Artery Occlusion 45 2.120
83
AND005 Androgen Insensitivity Syndrome, Mild 21 2.103
84
TWN001 Twin-to-Twin Transfusion Syndrome 46 2.065
85
P BRG001 Brugada Syndrome 69 2.065
86
BRN071 Brain Injury 50 2.010
87
SPN186 Spinal Cord Injury 61 1.971
88
MTB004 Metabolic Acidosis 48 1.971
89
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 1.971
90
HRT012 Heart Valve Disease 53 1.971
91
END086 End Stage Renal Disease 52 1.971
92
LNG099 Lung Disease 62 1.971
93
P END033 Endocarditis 58 1.971
94
INT053 Intracranial Vasospasm 36 1.937
95
P ANR048 Aniridia 1 64 1.924
96
MLT131 Multifocal Atrial Tachycardia 17 1.870
97
CRD223 Cardiac Arrhythmia 63 1.870
98
INF034 Infective Endocarditis 54 1.870
99
HYP066 Hyperglycemia 61 1.870
100
CHT001 Chaotic Atrial Tachycardia 10 1.870
101
SVR001 Severe Acute Respiratory Syndrome 67 1.805
102
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 1.759
103
P AMY004 Amyloidosis 70 1.759
104
CRN030 Coronary Stenosis 50 1.759
105
P ALC033 Alcohol Use Disorder 61 1.759
106
P MTR012 Mitral Valve Disease 57 1.759
107
BRK012 Broken Heart Syndrome 42 1.759
108
ACR041 Acromelic Frontonasal Dysostosis 53 1.692
109
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 1.692
110
ENT001 Enterocele 42 1.692
111
CVD001 Covid-19 57 1.661
112
ATR089 Atrioventricular Dissociation 21 1.637
113
TRM010 Traumatic Brain Injury 51 1.637
114
PLM033 Pulmonary Embolism 58 1.637
115
P VSC011 Vasculitis 61 1.585
116
ERL052 Early Repolarization Associated with Ventricular Fibrillation 22 1.499
117
INT007 Intermediate Coronary Syndrome 54 1.499
118
CRN019 Coronary Artery Vasospasm 47 1.499
119
PLM022 Pulmonary Valve Insufficiency 45 1.499
120
CYS001 Cystic Fibrosis 78 1.366
121
P HYP061 Hypertrophic Cardiomyopathy 69 1.366
122
WTH001 Withdrawal Disorder 48 1.335
123
P RNV001 Renovascular Hypertension 49 1.335
124
INF013 Inferior Myocardial Infarction 33 1.335
125
P DRM010 Dermatomyositis 61 1.335
126
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 1.334
127
DWN001 Down Syndrome 70 1.270
128
BRN056 Bronchopulmonary Dysplasia 56 1.270
129
P HYP098 Hypereosinophilic Syndrome 66 1.265
130
PRT036 Peritonitis 65 1.155
131
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 1.152
132
HYP458 Hyper Ige Syndrome 60 1.131
133
UNV002 Univentricular Heart 26 1.121
134
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.121
135
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.121
136
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.121
137
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 1.121
138
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 1.121
139
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 1.121
140
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.121
141
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 1.121
142
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.121
143
P LFT003 Left Ventricular Noncompaction 57 1.121
144
ACT003 Acute Kidney Tubular Necrosis 46 1.121
145
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 1.121
146
PRT013 Portal Hypertension 59 1.121
147
KWS002 Kawasaki Disease 65 1.056
148
CRB039 Cerebrovascular Disease 66 1.056
149
CYN002 Cyanosis, Transient Neonatal 43 1.033
150
c SPN286 Spinocerebellar Ataxia 40 29 1.033
151
MCN007 Meconium Aspiration Syndrome 53 1.033
152
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.894
153
AGN016 Aging 54 0.894
154
P BRC006 Brachydactyly 51 0.894
156
ENT011 Enterocolitis 55 0.894
157
P LCT001 Lactic Acidosis 51 0.894
158
P RST002 Restrictive Cardiomyopathy 54 0.894
159
CNS004 Constipation 56 0.894
160
PRM003 Premature Ejaculation 44 0.894
161
CHL014 Cholera 62 0.894
162
RHM001 Rheumatic Fever 59 0.894
163
CHR189 Chromosome 12p Deletion 12 0.894
164
PRN019 Perinatal Necrotizing Enterocolitis 60 0.894
165
THN005 Thunderclap Headache 15 0.730
166
P ALZ034 Alzheimer Disease 87 0.730
167
PRS129 Prostatic Hyperplasia, Benign 49 0.730
168
P PHC003 Pheochromocytoma 69 0.730
169
P EXN002 Exanthem 58 0.730
170
ATR057 Atrioventricular Block 54 0.730
171
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.730
172
BMB001 Bombay Phenotype 32 0.730
173
ADR040 Adrenal Gland Pheochromocytoma 46 0.730
174
PLM186 Pulmonary Arterial Hypertension Associated with Portal Hypertension 25 0.730
175
TXC010 Toxic Myocarditis 21 0.730
176
PNM008 Pneumothorax 54 0.730
177
SBC003 Subacute Bacterial Endocarditis 33 0.730
178
PRP009 Peripartum Cardiomyopathy 55 0.730
179
c PRC016 Pre-Eclampsia 65 0.730
180
ASP003 Aseptic Meningitis 50 0.730
181
PRS021 Prostatic Adenoma 43 0.730
182
P ATR010 Atrial Heart Septal Defect 58 0.730
183
PRS045 Prostatic Hypertrophy 53 0.730
184
TTN003 Tetanus 65 0.730
185
PLM031 Poliomyelitis 63 0.730
186
BRN002 Bronchiolitis 57 0.730
187
HTR003 Heterotaxy 43 0.730
188
HPR003 Heparin-Induced Thrombocytopenia 47 0.730
189
P ENC018 Encephalopathy 62 0.730
190
ATN005 Autonomic Dysfunction 46 0.730
191
CHR178 Chromosomal Triplication 34 0.730
192
P DBT009 Diabetes Mellitus 67 0.605
193
P EPL164 Epilepsy 68 0.605
194
P CNR004 Cone-Rod Dystrophy 2 74 0.540
195
P TRC087 Tricuspid Valve Disease 48 0.540
196
HYP025 Hyperphosphatemia 48 0.540
197
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 0.540
198
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.540
199
BLD051 Blood Coagulation Disease 53 0.540
200
P PRS038 Personality Disorder 65 0.540
201
CNN003 Conn's Syndrome 79 0.540
202
c ACT068 Acute Cystitis 61 0.540
203
P RRC004 Rare Cardiomyopathy 16 0.516
204
INT276 Interatrial Communication 51 0.516
205
VRS002 Virus-Associated Trichodysplasia Spinulosa 30 0.516
206
CRS011 Criss-Cross Heart 23 0.516
207
DBL010 Double-Orifice Mitral Valve 17 0.516
208
MCN018 Mucinous Adenocarcinoma of the Appendix 17 0.516
209
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 0.516
210
MSC152 Muscular Dystrophy, Becker Type 69 0.516
211
MRF001 Marfan Syndrome 76 0.516
212
MYC078 Myoclonus and Ataxia 32 0.516
213
c EXD008 Exudative Vitreoretinopathy 1 71 0.516
214
ATM095 Autoimmune Disease 61 0.516
215
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.516
216
P CLC063 Celiac Disease 1 66 0.516
217
HYD038 Hydrops Fetalis, Nonimmune 59 0.516
218
c LKM063 Leukemia, Chronic Myeloid 71 0.516
219
FML037 Female Breast Cancer 51 0.516
220
ATS010 Autosomal Recessive Disease 42 0.516
221
c MCR130 Microvascular Complications of Diabetes 6 41 0.516
222
DFC004 Deficiency Anemia 74 0.516
223
RNL025 Renal Hypoplasia 41 0.516
224
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.516
225
ART074 Aortic Dissection 53 0.516
226
APH002 Aphasia 56 0.516
227
RSP021 Respiratory Allergy 41 0.516
228
THR024 Thrombosis 56 0.516
229
RHM028 Rheumatic Heart Disease 56 0.516
230
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 0.516
231
KLD003 Keloid Formation 34 0.516
232
TRC062 Tricuspid Atresia 55 0.516
233
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.516
234
P LKM062 Leukemia, Acute Lymphoblastic 69 0.516
235
LPT014 Leptin Deficiency or Dysfunction 78 0.516
236
c SPN418 Spinocerebellar Ataxia 44 26 0.516
237
c SPN323 Spinocerebellar Ataxia 41 23 0.516
238
c MCR120 Microvascular Complications of Diabetes 7 47 0.516
239
THR100 Thrombocytopenic Purpura, Autoimmune 61 0.516
240
OST159 Osteogenic Sarcoma 66 0.516
241
THY111 Thyroid Carcinoma, Familial Medullary 67 0.516
242
PNM010 Pneumothorax, Primary Spontaneous 58 0.516
243
PNG002 Pain Agnosia 51 0.516
244
ARG004 Argyria 26 0.516
245
THY029 Thyroid Carcinoma 51 0.516
246
c CRB219 Cerebellar Ataxia Type 41 24 0.516
247
HPT009 Hepatopulmonary Syndrome 48 0.516
248
P NRB001 Neuroblastoma 66 0.516
249
EXT007 Extracutaneous Mastocytoma 38 0.516
250
P MYP004 Myopathy 67 0.516
251
AKN002 Akinetic Mutism 36 0.516
252
STT002 Status Asthmaticus 49 0.516
253
LRN003 Learning Disability 49 0.516
254
VRL011 Viral Infectious Disease 61 0.516
255
APP009 Appendix Adenocarcinoma 45 0.516
256
P TRM003 Tremor 48 0.516
257
MST004 Mast Cell Neoplasm 42 0.516
258
c ACT076 Acute Myocarditis 47 0.516
259
MCN001 Mucinous Adenocarcinoma 49 0.516
260
GLB002 Glioblastoma 67 0.516
261
PRC013 Pericarditis 53 0.516
262
THY125 Thyroid Gland Medullary Carcinoma 48 0.516
263
MTS001 Mutism 44 0.516
264
P ESN008 Eosinophilic Pneumonia 50 0.516
265
CNN005 Connective Tissue Disease 67 0.516
266
P PLY018 Polycythemia 56 0.516
267
CMM005 Common Cold 56 0.516
268
c MCR113 Microvascular Complications of Diabetes 3 52 0.516
269
c MCR133 Microvascular Complications of Diabetes 4 41 0.516
270
CRN017 Coronary Thrombosis 46 0.516
271
ALL029 Allergic Disease 59 0.516
272
OLG003 Oligohydramnios 51 0.516
273
P LKM002 Leukemia 67 0.516
274
CRT013 Carotid Stenosis 51 0.516
275
PRV004 Periventricular Leukomalacia 52 0.516
276
BLR008 Bilirubin Metabolic Disorder 57 0.516
277
BLR001 Biliary Atresia 55 0.516
278
CHL056 Cheilitis 46 0.516
279
P HYP086 Hypothyroidism 69 0.516
280
P ECL001 Eclampsia 52 0.516
281
IRN001 Iron Deficiency Anemia 58 0.516
282
CRD001 Cardiac Tamponade 43 0.516
283
ASP004 Asphyxia Neonatorum 50 0.516
284
CNS002 Constrictive Pericarditis 40 0.516
285
P CNJ013 Conjunctivitis 66 0.516
286
LVR012 Liver Cirrhosis 63 0.516
287
P PNM007 Pneumonia 67 0.516
288
PRP030 Purpura 54 0.516
289
P MLT074 Multiple Endocrine Neoplasia 59 0.516
290
MXD005 Mixed Connective Tissue Disease 57 0.516
291
PTN001 Patent Foramen Ovale 62 0.516
292
CPL003 Capillary Leak Syndrome 54 0.516
293
ECT004 Ecthyma 26 0.516
294
VRT001 Vertebral Artery Occlusion 29 0.516
295
QDR001 Quadriplegia 50 0.516
296
IRN002 Iron Metabolism Disease 57 0.516
297
KLD004 Keloid Disorder 39 0.516
298
PLM035 Pulmonary Eosinophilia 49 0.516
299
P CMP008 Compartment Syndrome 50 0.516
300
INH007 Inherited Thyroxine-Binding Globulin Deficiency 13 0.516
301
P MYC033 Myoclonus 47 0.516
302
P FML187 Familial Hypertension 34 0.516
303
P ART034 Aortopulmonary Window 21 0.516
304
ESN011 Eisenmenger Syndrome 47 0.516
305
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 45 0.516
306
SBC016 Subacute Delirium 43 0.516
The MalaCards human disease database index: 1-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
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