Search results for Irbesartan

216 hits were found for Irbesartan

# Family MCID Name MIFTS Score
1
c HYP595 Hypertension, Essential 84 0.525
2
c MCR113 Microvascular Complications of Diabetes 3 52 0.402
3
c MCR120 Microvascular Complications of Diabetes 7 47 0.396
4
c MCR130 Microvascular Complications of Diabetes 6 41 0.396
5
c MCR133 Microvascular Complications of Diabetes 4 41 0.396
6
P KDN018 Kidney Disease 70 0.278
7
END030 End Stage Renal Failure 58 0.238
8
P ATR011 Atrial Fibrillation 66 0.211
9
P HRT032 Heart Disease 75 0.195
10
CNG034 Congestive Heart Failure 70 0.190
11
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.185
12
c CHR684 Chronic Kidney Disease 66 0.181
13
ATH013 Atherosclerosis Susceptibility 66 0.150
14
CRB039 Cerebrovascular Disease 69 0.144
15
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.138
16
c FML001 Familial Atrial Fibrillation 66 0.138
17
P MCR115 Microvascular Complications of Diabetes 5 66 0.138
18
P DBT009 Diabetes Mellitus 64 0.138
19
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.138
20
MSC007 Muscle Hypertrophy 63 0.138
21
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.138
22
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.138
23
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.138
24
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.138
25
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.138
26
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.138
27
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.138
28
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.138
29
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.138
30
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.138
31
c MCR129 Microvascular Complications of Diabetes 1 66 0.131
32
c MCR112 Microvascular Complications of Diabetes 2 41 0.131
33
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.124
34
STR067 Stroke, Ischemic 80 0.124
35
c HYP836 Hypercholesterolemia, Familial, 1 72 0.124
36
P MYC007 Myocardial Infarction 70 0.124
37
P GLM007 Glomerulonephritis 57 0.124
38
c RHB024 Rhabdomyosarcoma 2 65 0.117
39
P CRN018 Coronary Artery Anomaly 63 0.117
40
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.117
41
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.117
42
c FML035 Familial Hyperlipidemia 55 0.117
43
HYP005 Hypokalemia 55 0.117
44
48X005 48,xyyy 39 0.117
45
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.117
46
c ATR087 Atrial Standstill 1 74 0.110
47
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.110
48
P CRD246 Cardiovascular System Disease 56 0.110
49
CYT002 Cytokine Deficiency 44 0.110
50
MRF001 Marfan Syndrome 75 0.102
51
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.102
52
P TRN020 Turner Syndrome 65 0.102
53
P CRN300 Coronary Heart Disease 1 63 0.102
54
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.102
55
LPD008 Lipid Metabolism Disorder 62 0.102
56
HYP014 Hyperuricemia 51 0.102
57
IGG001 Iga Glomerulonephritis 48 0.102
58
LPT014 Leptin Deficiency or Dysfunction 73 0.093
59
P HPT021 Hepatitis 67 0.093
60
P NPH012 Nephrotic Syndrome 63 0.093
61
TRN015 Transient Cerebral Ischemia 62 0.093
62
NTR005 Nutritional Deficiency Disease 61 0.093
63
ISC004 Ischemia 60 0.093
64
P FCL005 Focal Segmental Glomerulosclerosis 58 0.093
65
c ACT075 Acute Myocardial Infarction 56 0.093
66
INT007 Intermediate Coronary Syndrome 55 0.093
67
ART140 Arteries, Anomalies of 53 0.093
68
HYP081 Hypolipoproteinemia 50 0.093
69
c DLT002 Dilated Cardiomyopathy 79 0.083
70
ANG054 Angina Pectoris 66 0.083
71
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 58 0.083
72
P HDC001 Headache 57 0.083
73
MRD002 Marden-Walker Syndrome 55 0.083
74
LPT006 Leptin Receptor Deficiency 47 0.083
75
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.083
76
c FCL025 Focal Segmental Glomerulosclerosis 1 47 0.083
77
c HYP272 Hypercholesterolemia, Familial, 3 43 0.083
78
DFC004 Deficiency Anemia 75 0.072
79
RCK004 Rickets 69 0.072
80
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.072
81
ALL026 Allergic Hypersensitivity Disease 64 0.072
82
LVR012 Liver Cirrhosis 63 0.072
83
P HYP750 Hypertriglyceridemia, Familial 61 0.072
84
FTT001 Fatty Liver Disease 61 0.072
85
HYP066 Hyperglycemia 61 0.072
86
PRT013 Portal Hypertension 60 0.072
87
P BCL017 B-Cell Lymphoma 58 0.072
88
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.072
89
P SCK002 Sick Sinus Syndrome 55 0.072
90
P ART021 Arteriosclerosis 54 0.072
91
GLC003 Glucose Intolerance 54 0.072
92
IMP005 Impotence 52 0.072
93
c VRL010 Viral Hepatitis 51 0.072
94
SYS003 Systolic Heart Failure 50 0.072
95
HYP006 Hypertensive Heart Disease 49 0.072
96
P IGN003 Iga Nephropathy 1 49 0.072
97
URM002 Uremia 49 0.072
98
SNT005 Sinoatrial Node Disease 49 0.072
99
SXL003 Sexual Disorder 48 0.072
100
RNL077 Renal Fibrosis 47 0.072
101
CRB004 Cerebral Artery Occlusion 44 0.072
102
P STR092 Striatal Degeneration, Autosomal Dominant 2 43 0.072
103
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.072
104
HYP540 Hypertension, Diastolic 40 0.072
105
c NPH047 Nephrotic Syndrome, Type 4 32 0.072
106
P SCH015 Schizophrenia 75 0.059
107
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.059
108
PRP027 Peripheral Vascular Disease 71 0.059
109
DWN001 Down Syndrome 70 0.059
110
MLN008 Melanoma 69 0.059
111
P SLP006 Sleep Apnea 69 0.059
112
SKN019 Skin Melanoma 67 0.059
113
APN008 Apnea, Obstructive Sleep 65 0.059
114
GT001 Gout 63 0.059
115
P VSC007 Vascular Disease 63 0.059
116
c PRC016 Pre-Eclampsia 63 0.059
117
DPR016 Depression 63 0.059
118
c HPT001 Hepatitis C 63 0.059
119
c HPT003 Hepatitis a 63 0.059
120
P HYP069 Hyperparathyroidism 62 0.059
121
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.059
122
VRL011 Viral Infectious Disease 61 0.059
123
CHL068 Cholestasis 60 0.059
124
CRD223 Cardiac Arrhythmia 60 0.059
125
c ACT071 Acute Kidney Failure 59 0.059
126
ANR040 Aneurysm 58 0.059
127
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.059
128
P EXN002 Exanthem 57 0.059
129
P EHL001 Ehlers-Danlos Syndrome 57 0.059
130
MNT002 Mental Depression 57 0.059
131
EHL052 Ehlers-Danlos Syndrome, Vascular Type 56 0.059
132
P ECL001 Eclampsia 51 0.059
133
c SCN007 Secondary Hyperparathyroidism 50 0.059
134
47X002 47,xyy 49 0.059
135
P RNV001 Renovascular Hypertension 49 0.059
136
VTM033 Vitamin K Deficiency Bleeding 48 0.059
137
P RNL015 Renal Hypertension 48 0.059
138
ATX019 Ataxia with Vitamin E Deficiency 48 0.059
139
HYP025 Hyperphosphatemia 47 0.059
140
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.059
141
EBL001 Ebola Hemorrhagic Fever 46 0.059
142
SYN036 Syncope 45 0.059
143
LKS001 Leukostasis 44 0.059
144
DST006 Diastolic Heart Failure 44 0.059
145
c PRM038 Primary Agammaglobulinemia 43 0.059
146
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 42 0.059
147
RDN001 Reading Disorder 40 0.059
148
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.059
149
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.059
150
P PRC031 Preeclampsia/eclampsia 1 37 0.059
151
KDN013 Kidney Hypertrophy 34 0.059
152
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.059
153
P CLR023 Colorectal Cancer 98 0.041
154
PLM134 Pulmonary Fibrosis, Idiopathic 75 0.041
155
P OST002 Osteoporosis 73 0.041
156
ANX010 Anxiety 72 0.041
157
SCK003 Sickle Cell Anemia 72 0.041
158
c MGR028 Migraine with or Without Aura 1 69 0.041
159
P PLM037 Pulmonary Hypertension 68 0.041
160
c PRG042 Progressive Familial Heart Block, Type Ia 67 0.041
161
P DMN002 Dementia 67 0.041
162
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.041
163
PRT036 Peritonitis 65 0.041
164
KHL003 Kohlschutter-Tonz Syndrome 64 0.041
165
IRR002 Irritable Bowel Syndrome 63 0.041
166
IDP011 Idiopathic Interstitial Pneumonia 63 0.041
167
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.041
168
P PLM036 Pulmonary Fibrosis 61 0.041
169
INT002 Intermittent Claudication 61 0.041
170
LNG099 Lung Disease 61 0.041
171
P PNC044 Pancreatitis 61 0.041
172
c ACT027 Acute Pancreatitis 59 0.041
173
CRD132 Cardiac Conduction Defect 59 0.041
174
c PRG043 Progressive Familial Heart Block, Type Ib 58 0.041
175
CNS004 Constipation 57 0.041
176
ERY003 Erythema Multiforme 57 0.041
177
VSC002 Vascular Dementia 57 0.041
178
P NRP001 Neuropathy 56 0.041
179
AGN016 Aging 56 0.041
180
ALL006 Allergic Asthma 56 0.041
181
BRN004 Brain Edema 55 0.041
182
c GRV008 Graves Disease 1 55 0.041
183
PLM010 Pulmonary Edema 55 0.041
184
P ANG015 Angioedema 54 0.041
185
GST037 Gastroparesis 53 0.041
186
RHM028 Rheumatic Heart Disease 53 0.041
187
GST023 Gastric Ulcer 53 0.041
188
PRP080 Peripheral Artery Disease 53 0.041
189
PNG002 Pain Agnosia 51 0.041
190
NNL006 Non-Alcoholic Steatohepatitis 51 0.041
191
P MMB011 Membranous Nephropathy 50 0.041
192
P SCK005 Sickle Cell Disease 50 0.041
193
BRN071 Brain Injury 49 0.041
194
NPH010 Nephrosclerosis 49 0.041
195
LFT001 Left Bundle Branch Hemiblock 49 0.041
196
PRN009 Paranoid Schizophrenia 49 0.041
197
P OBS001 Obstructive Jaundice 48 0.041
198
P MGR001 Migraine Without Aura 48 0.041
199
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.041
200
RGH001 Right Bundle Branch Block 47 0.041
201
P CRC039 Coarctation of Aorta 47 0.041
202
URT010 Ureteral Obstruction 46 0.041
203
DBT008 Diabetic Angiopathy 44 0.041
204
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.041
205
NSP002 Nasopharyngitis 41 0.041
206
RST023 Resting Heart Rate, Variation in 41 0.041
207
SPR126 Superior Semicircular Canal Dehiscence 40 0.041
208
ANG049 Angioedema Induced by Ace Inhibitors 40 0.041
209
c HMG029 Hemoglobin Se Disease 38 0.041
210
RNL001 Renal Artery Obstruction 33 0.041
211
c RNG022 Ring Chromosome 6 28 0.041
212
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.041
213
c RNG021 Ring Chromosome 5 23 0.041
214
DPS001 Dipsogenic Diabetes Insipidus 23 0.041
215
OBS529 Obsolete: Combined Hyperlipidemia 22 0.041
216
SPR033 Superficial Spreading Melanoma 18 0.041
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