Search results for Ranolazine

181 hits were found for Ranolazine

# Family MCID Name MIFTS Score
1
ANG054 Angina Pectoris 66 0.533
2
ISC004 Ischemia 60 0.448
3
P CRN018 Coronary Artery Anomaly 63 0.411
4
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.372
5
P ATR011 Atrial Fibrillation 66 0.366
6
ART140 Arteries, Anomalies of 53 0.361
7
P CRN300 Coronary Heart Disease 1 63 0.333
8
P HRT032 Heart Disease 75 0.309
9
P DBT009 Diabetes Mellitus 64 0.233
10
c FML001 Familial Atrial Fibrillation 66 0.225
11
c ATR087 Atrial Standstill 1 74 0.221
12
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.216
13
P LNG028 Long Qt Syndrome 65 0.216
14
CNG034 Congestive Heart Failure 70 0.207
15
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.202
16
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.197
17
CRD132 Cardiac Conduction Defect 59 0.182
18
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.176
19
P PLM037 Pulmonary Hypertension 68 0.176
20
CNS004 Constipation 57 0.171
21
c HYP595 Hypertension, Essential 84 0.159
22
P MYC007 Myocardial Infarction 70 0.153
23
P HYP061 Hypertrophic Cardiomyopathy 66 0.153
24
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 62 0.153
25
DST006 Diastolic Heart Failure 44 0.146
26
c LNG048 Long Qt Syndrome 3 52 0.139
27
STR067 Stroke, Ischemic 80 0.132
28
PRP027 Peripheral Vascular Disease 71 0.132
29
CRB039 Cerebrovascular Disease 69 0.132
30
INT002 Intermittent Claudication 61 0.132
31
HYP066 Hyperglycemia 61 0.132
32
c PNS012 Paine Syndrome 61 0.132
33
P KDN018 Kidney Disease 70 0.125
34
HYP056 Hypoglycemia 66 0.125
35
HYP005 Hypokalemia 55 0.125
36
INT007 Intermediate Coronary Syndrome 55 0.125
37
CRN030 Coronary Stenosis 50 0.125
38
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.125
39
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.125
40
P TRN020 Turner Syndrome 65 0.117
41
CRD223 Cardiac Arrhythmia 60 0.117
42
MYT011 Myotonia 35 0.117
43
ATH013 Atherosclerosis Susceptibility 66 0.108
44
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.108
45
P VSC007 Vascular Disease 63 0.108
46
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.108
47
P CRD246 Cardiovascular System Disease 56 0.108
48
PRP080 Peripheral Artery Disease 53 0.108
49
ADL002 Adult Syndrome 69 0.099
50
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 67 0.099
51
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.099
52
c CHR684 Chronic Kidney Disease 66 0.099
53
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.099
54
c RHB024 Rhabdomyosarcoma 2 65 0.099
55
MSC007 Muscle Hypertrophy 63 0.099
56
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.099
57
c FML191 Familial Long Qt Syndrome 53 0.099
58
SYS003 Systolic Heart Failure 50 0.099
59
PRM057 Paramyotonia Congenita of Von Eulenburg 46 0.099
60
HRT015 Heritable Pulmonary Arterial Hypertension 44 0.099
61
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.099
62
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 42 0.099
63
HYP540 Hypertension, Diastolic 40 0.099
64
CRD170 Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 1 40 0.099
65
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.088
66
c DLT002 Dilated Cardiomyopathy 79 0.088
67
P CNR004 Cone-Rod Dystrophy 2 71 0.088
68
P MTR014 Motor Neuron Disease 64 0.088
69
END030 End Stage Renal Failure 58 0.088
70
c ACT075 Acute Myocardial Infarction 56 0.088
71
P MYT023 Myotonia Congenita 55 0.088
72
P LTR001 Lateral Sclerosis 53 0.088
73
c PRM092 Primary Lateral Sclerosis, Adult, 1 52 0.088
74
c SHR030 Short Qt Syndrome 48 0.088
75
MYC005 Myocardial Stunning 46 0.088
76
48X005 48,xyyy 39 0.088
77
P PRS040 Prostate Cancer 97 0.076
78
DWN001 Down Syndrome 70 0.076
79
c MGR028 Migraine with or Without Aura 1 69 0.076
80
c MYT021 Myotonic Dystrophy 1 66 0.076
81
c MCR129 Microvascular Complications of Diabetes 1 66 0.076
82
P NRV007 Nervous System Disease 66 0.076
83
P MYP004 Myopathy 64 0.076
84
P ADN016 Adenocarcinoma 64 0.076
85
IRR002 Irritable Bowel Syndrome 63 0.076
86
LPD008 Lipid Metabolism Disorder 62 0.076
87
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.076
88
P PRP019 Peripheral Nervous System Disease 57 0.076
89
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.076
90
c MYT020 Myotonic Dystrophy 2 57 0.076
91
P DRR001 Diarrhea 57 0.076
92
P NRP001 Neuropathy 56 0.076
93
P PLY019 Polyneuropathy 56 0.076
94
P SCK002 Sick Sinus Syndrome 55 0.076
95
c MYP132 Myopathy, Congenital 55 0.076
96
DBT010 Diabetic Neuropathy 55 0.076
97
P MYT002 Myotonic Dystrophy 49 0.076
98
ATX019 Ataxia with Vitamin E Deficiency 48 0.076
99
c MTR002 Mitral Valve Insufficiency 47 0.076
100
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.076
101
ATN004 Autonomic Neuropathy 44 0.076
102
DBT002 Diabetic Autonomic Neuropathy 41 0.076
103
RST023 Resting Heart Rate, Variation in 41 0.076
104
c MYT029 Myotonia Congenita, Autosomal Recessive 41 0.076
105
MYT003 Myotonic Disease 37 0.076
106
c PRS136 Prostate Cancer, Hereditary, 6 33 0.076
107
c PRS130 Prostate Cancer, Hereditary, 8 32 0.076
108
CYT018 Cytochrome P450 2d6 Variant 27 0.076
109
IMM167 Immune Deficiency Disease 78 0.062
110
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.062
111
ALL026 Allergic Hypersensitivity Disease 64 0.062
112
TMT001 Timothy Syndrome 62 0.062
113
TRN015 Transient Cerebral Ischemia 62 0.062
114
LNG099 Lung Disease 61 0.062
115
P EXN002 Exanthem 57 0.062
116
HYP266 Hypoxia 56 0.062
117
LMB062 Limb Ischemia 55 0.062
118
P ART021 Arteriosclerosis 54 0.062
119
INS023 Insensitivity to Pain, Congenital, with Anhidrosis 54 0.062
120
P TRM003 Tremor 53 0.062
121
47X002 47,xyy 49 0.062
122
SNT005 Sinoatrial Node Disease 49 0.062
123
P ERY008 Erythromelalgia 47 0.062
124
P MYC033 Myoclonus 46 0.062
125
CHL079 Children's Interstitial Lung Disease 27 0.062
126
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.044
127
c HYP836 Hypercholesterolemia, Familial, 1 72 0.044
128
P AMY004 Amyloidosis 70 0.044
129
P BRG001 Brugada Syndrome 70 0.044
130
P HYP086 Hypothyroidism 68 0.044
131
P LVR013 Liver Disease 68 0.044
132
P CRD119 Cardiac Arrest 67 0.044
133
c PRG042 Progressive Familial Heart Block, Type Ia 67 0.044
134
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.044
135
FTT001 Fatty Liver Disease 61 0.044
136
ERL001 Early Myoclonic Encephalopathy 61 0.044
137
PLM033 Pulmonary Embolism 59 0.044
138
c LNG047 Long Qt Syndrome 2 58 0.044
139
P SZR006 Seizure Disorder 58 0.044
140
P FCL005 Focal Segmental Glomerulosclerosis 58 0.044
141
VSL002 Visual Epilepsy 58 0.044
142
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.044
143
P RST002 Restrictive Cardiomyopathy 56 0.044
144
SLC006 Silicosis 56 0.044
145
ATR057 Atrioventricular Block 55 0.044
146
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.044
147
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 54 0.044
148
P ANG015 Angioedema 54 0.044
149
GLC003 Glucose Intolerance 54 0.044
150
c FML023 Familial Hemiplegic Migraine 54 0.044
151
PRC013 Pericarditis 54 0.044
152
PRX015 Paroxysmal Extreme Pain Disorder 53 0.044
153
PRG009 Progressive Multifocal Leukoencephalopathy 53 0.044
154
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.044
155
IMP005 Impotence 52 0.044
156
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.044
157
P FBR031 Febrile Seizures 51 0.044
158
LFT001 Left Bundle Branch Hemiblock 49 0.044
159
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.044
160
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.044
161
P CRC039 Coarctation of Aorta 47 0.044
162
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.044
163
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.044
164
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.044
165
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.044
166
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.044
167
P HMP006 Hemiplegic Migraine 44 0.044
168
PTT037 Pituitary Tumors 44 0.044
169
SBC016 Subacute Delirium 44 0.044
170
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.044
171
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.044
172
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.044
173
c RTN047 Retinitis Pigmentosa 18 44 0.044
174
P HYP265 Hypotonia 42 0.044
175
c CTR132 Cataract 3, Multiple Types 40 0.044
176
ACT167 Acute Generalized Exanthematous Pustulosis 37 0.044
177
c MYC068 Myoclonic Epilepsy of Infancy 37 0.044
178
c SHR031 Short Qt Syndrome 1 29 0.044
179
GNT046 Genetic Epilepsy with Febrile Seizures Plus 28 0.044
180
c LNG052 Long Qt Syndrome 8 26 0.044
181
MSC193 Muscular Lipidosis 23 0.044
Content
Loading form....