Search results for Perindopril

197 hits were found for Perindopril

# Family MCID Name MIFTS Score
1
c HYP595 Hypertension, Essential 84 0.571
2
CNG034 Congestive Heart Failure 69 0.309
3
CRB039 Cerebrovascular Disease 67 0.275
4
LPP008 Lipoprotein Quantitative Trait Locus 62 0.275
5
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.268
6
P HRT032 Heart Disease 75 0.262
7
ART140 Arteries, Anomalies of 52 0.258
8
P CRN300 Coronary Heart Disease 1 63 0.229
9
c MCR113 Microvascular Complications of Diabetes 3 52 0.208
10
c MCR120 Microvascular Complications of Diabetes 7 47 0.208
11
c MCR130 Microvascular Complications of Diabetes 6 41 0.208
12
c MCR133 Microvascular Complications of Diabetes 4 41 0.208
13
P KDN018 Kidney Disease 72 0.204
14
P VSC007 Vascular Disease 63 0.204
15
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.185
16
STR067 Stroke, Ischemic 81 0.164
17
P DBT009 Diabetes Mellitus 64 0.164
18
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.159
19
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.159
20
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.159
21
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.159
22
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.159
23
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.159
24
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.159
25
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.159
26
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.159
27
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.159
28
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.159
29
c CHR684 Chronic Kidney Disease 70 0.147
30
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.147
31
HYP005 Hypokalemia 55 0.147
32
P CRD119 Cardiac Arrest 67 0.141
33
c ACT075 Acute Myocardial Infarction 57 0.141
34
c ATR087 Atrial Standstill 1 75 0.134
35
P MYC007 Myocardial Infarction 70 0.134
36
ATH013 Atherosclerosis Susceptibility 65 0.134
37
c DLT002 Dilated Cardiomyopathy 79 0.127
38
ANG054 Angina Pectoris 66 0.127
39
P ATR011 Atrial Fibrillation 66 0.127
40
CRD223 Cardiac Arrhythmia 60 0.120
41
P CRD246 Cardiovascular System Disease 57 0.120
42
P RNV001 Renovascular Hypertension 48 0.120
43
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.120
44
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.120
45
MRF001 Marfan Syndrome 77 0.112
46
c HYP836 Hypercholesterolemia, Familial, 1 73 0.112
47
P MCR115 Microvascular Complications of Diabetes 5 66 0.112
48
LPD008 Lipid Metabolism Disorder 62 0.112
49
48X005 48,xyyy 39 0.112
50
MSC007 Muscle Hypertrophy 64 0.104
51
DWN001 Down Syndrome 70 0.095
52
P LVR013 Liver Disease 68 0.095
53
c FML001 Familial Atrial Fibrillation 65 0.095
54
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.095
55
TRN015 Transient Cerebral Ischemia 63 0.095
56
PRT058 Pure Autonomic Failure 59 0.095
57
ISC004 Ischemia 58 0.095
58
P ANG015 Angioedema 57 0.095
59
END086 End Stage Renal Disease 51 0.095
60
HYP540 Hypertension, Diastolic 40 0.095
61
MSC157 Muscular Dystrophy, Duchenne Type 72 0.085
62
P MSC005 Muscular Dystrophy 66 0.085
63
c MCR129 Microvascular Complications of Diabetes 1 66 0.085
64
ALL026 Allergic Hypersensitivity Disease 62 0.085
65
LVR012 Liver Cirrhosis 62 0.085
66
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.085
67
EYD002 Eye Disease 58 0.085
68
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.085
69
MRD002 Marden-Walker Syndrome 56 0.085
70
c MCR112 Microvascular Complications of Diabetes 2 41 0.085
71
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.085
72
P CLR023 Colorectal Cancer 99 0.074
73
P ALZ034 Alzheimer Disease 88 0.074
74
P PRK057 Parkinson Disease, Late-Onset 78 0.074
75
AST005 Asthma 76 0.074
76
P OST002 Osteoporosis 74 0.074
77
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.074
78
ART016 Aortic Aneurysm 69 0.074
79
P CMP005 Campomelic Dysplasia 64 0.074
80
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.074
81
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.074
82
FTT001 Fatty Liver Disease 61 0.074
83
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.074
84
ANR040 Aneurysm 59 0.074
85
VSC002 Vascular Dementia 57 0.074
86
INT007 Intermediate Coronary Syndrome 55 0.074
87
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.074
88
NNL006 Non-Alcoholic Steatohepatitis 54 0.074
89
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.074
90
ART074 Aortic Dissection 52 0.074
91
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.074
92
c CRD233 Cardiomyopathy, Dilated, 1b 45 0.074
93
c HYP272 Hypercholesterolemia, Familial, 3 44 0.074
94
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.074
95
ATX019 Ataxia with Vitamin E Deficiency 42 0.074
96
c MSC050 Muscular Dystrophy, Congenital, 1b 38 0.074
97
P BRS047 Breast Cancer 97 0.060
98
PRP027 Peripheral Vascular Disease 71 0.060
99
P HYP086 Hypothyroidism 69 0.060
100
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.060
101
P PLM037 Pulmonary Hypertension 67 0.060
102
P DMN002 Dementia 66 0.060
103
MSM014 Mismatch Repair Cancer Syndrome 65 0.060
104
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.060
105
c DBT099 Diabetes Mellitus, Type I 65 0.060
106
HYP066 Hyperglycemia 61 0.060
107
P PNC044 Pancreatitis 61 0.060
108
LNG099 Lung Disease 60 0.060
109
P MYC008 Myocarditis 59 0.060
110
P ANP001 Anaplastic Large Cell Lymphoma 58 0.060
111
PST028 Post-Traumatic Stress Disorder 58 0.060
112
P BCL017 B-Cell Lymphoma 58 0.060
113
AGN016 Aging 56 0.060
114
P SBS003 Substance Abuse 55 0.060
115
HYP060 Hyperinsulinism 54 0.060
116
P ART021 Arteriosclerosis 54 0.060
117
HYP014 Hyperuricemia 52 0.060
118
DYS073 Dysphagia 50 0.060
119
P ART018 Aortic Valve Insufficiency 49 0.060
120
47X002 47,xyy 49 0.060
121
BNR002 Bone Resorption Disease 48 0.060
122
c MLG069 Malignant Hypertension 47 0.060
123
ACT084 Acute Stress Disorder 47 0.060
124
49X006 49, Xxxxy Syndrome 41 0.060
125
PLY100 Polyploidy 40 0.060
126
P FML187 Familial Hypertension 37 0.060
127
URT049 Urate Oxidase, Pseudogene 25 0.060
128
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.042
129
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.042
130
P MYP004 Myopathy 70 0.042
131
BRN024 Bronchitis 68 0.042
132
RCK004 Rickets 68 0.042
133
P HYP098 Hypereosinophilic Syndrome 67 0.042
134
c RHB024 Rhabdomyosarcoma 2 67 0.042
135
P PLM036 Pulmonary Fibrosis 65 0.042
136
TTN003 Tetanus 65 0.042
137
PRT036 Peritonitis 64 0.042
138
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.042
139
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.042
140
c SVR001 Severe Acute Respiratory Syndrome 62 0.042
141
CHL068 Cholestasis 61 0.042
143
P ENC018 Encephalopathy 61 0.042
144
P NPH012 Nephrotic Syndrome 60 0.042
145
c ACT027 Acute Pancreatitis 60 0.042
146
c ACT071 Acute Kidney Failure 60 0.042
147
PRT013 Portal Hypertension 59 0.042
148
P BND020 Bone Disease 59 0.042
149
CNS004 Constipation 58 0.042
150
P GLM007 Glomerulonephritis 57 0.042
151
P EXN002 Exanthem 57 0.042
152
THR024 Thrombosis 57 0.042
153
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.042
154
P FCL005 Focal Segmental Glomerulosclerosis 57 0.042
155
P NRP001 Neuropathy 56 0.042
156
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.042
157
MMB001 Membranoproliferative Glomerulonephritis 55 0.042
158
P SCL048 Sclerosteosis 55 0.042
159
GLC003 Glucose Intolerance 54 0.042
160
PLM010 Pulmonary Edema 54 0.042
161
HRT012 Heart Valve Disease 53 0.042
162
OCL006 Ocular Hypertension 53 0.042
163
P DDN001 Duodenal Ulcer 52 0.042
164
PNG002 Pain Agnosia 51 0.042
165
OCL069 Ocular Motor Apraxia 51 0.042
166
SYS003 Systolic Heart Failure 49 0.042
167
HYP006 Hypertensive Heart Disease 49 0.042
168
BRN071 Brain Injury 49 0.042
169
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.042
170
RNL077 Renal Fibrosis 47 0.042
171
HYP034 Hypertensive Encephalopathy 46 0.042
172
RTN020 Retinal Vascular Disease 46 0.042
173
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 46 0.042
174
DST006 Diastolic Heart Failure 45 0.042
175
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.042
176
CRT015 Carotid Artery Occlusion 45 0.042
177
GRN017 Granulocytopenia 44 0.042
178
CVD001 Covid-19 44 0.042
179
MND023 Mend Syndrome 43 0.042
180
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.042
181
P HYP265 Hypotonia 43 0.042
182
BNS003 Binswanger's Disease 42 0.042
183
CYT002 Cytokine Deficiency 42 0.042
184
c RTN047 Retinitis Pigmentosa 18 42 0.042
185
RST023 Resting Heart Rate, Variation in 41 0.042
186
RDN001 Reading Disorder 40 0.042
187
c FRN049 Frontometaphyseal Dysplasia 1 40 0.042
188
ANG049 Angioedema Induced by Ace Inhibitors 40 0.042
189
HYP008 Hypertensive Retinopathy 39 0.042
190
GLM044 Glomerular Disease 37 0.042
191
HYP114 Hypertensive Nephropathy 36 0.042
192
c FRN048 Frontometaphyseal Dysplasia 2 35 0.042
193
c ATM022 Autoimmune Myocarditis 35 0.042
194
PLT015 Platelet Aggregation, Spontaneous 34 0.042
195
SLN001 Silent Myocardial Infarction 34 0.042
196
KDN013 Kidney Hypertrophy 32 0.042
197
CGH002 Cough Headache 21 0.042
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