Search results for Ramipril

272 hits were found for Ramipril

# Family MCID Name MIFTS Score
1
c HYP595 Hypertension, Essential 84 0.532
2
P KDN018 Kidney Disease 72 0.305
3
CNG034 Congestive Heart Failure 69 0.300
4
c MCR113 Microvascular Complications of Diabetes 3 52 0.259
5
c MCR120 Microvascular Complications of Diabetes 7 47 0.259
6
c MCR130 Microvascular Complications of Diabetes 6 41 0.259
7
c MCR133 Microvascular Complications of Diabetes 4 41 0.259
8
P VSC007 Vascular Disease 63 0.233
9
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.230
10
P MYC007 Myocardial Infarction 70 0.220
11
P HRT032 Heart Disease 75 0.210
12
P DBT009 Diabetes Mellitus 64 0.210
13
c CHR684 Chronic Kidney Disease 70 0.207
14
P CRD246 Cardiovascular System Disease 57 0.207
15
c ACT075 Acute Myocardial Infarction 57 0.196
16
END086 End Stage Renal Disease 51 0.196
17
PRP027 Peripheral Vascular Disease 71 0.185
18
LPP008 Lipoprotein Quantitative Trait Locus 62 0.177
19
ART140 Arteries, Anomalies of 52 0.173
20
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.169
21
ATH013 Atherosclerosis Susceptibility 65 0.169
22
P MCR115 Microvascular Complications of Diabetes 5 66 0.165
23
c MCR129 Microvascular Complications of Diabetes 1 66 0.165
24
c MCR112 Microvascular Complications of Diabetes 2 41 0.165
25
STR067 Stroke, Ischemic 81 0.160
26
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.160
27
CRB039 Cerebrovascular Disease 67 0.160
28
P CRN300 Coronary Heart Disease 1 63 0.160
29
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.156
30
INT002 Intermittent Claudication 61 0.156
31
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.151
32
P TRN020 Turner Syndrome 67 0.141
33
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.141
34
ISC004 Ischemia 58 0.131
35
PRP080 Peripheral Artery Disease 53 0.131
36
ATX019 Ataxia with Vitamin E Deficiency 42 0.131
37
ADL002 Adult Syndrome 70 0.125
38
ANG054 Angina Pectoris 66 0.125
39
P ATR011 Atrial Fibrillation 66 0.125
40
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.125
41
P ANG015 Angioedema 57 0.125
42
HYP005 Hypokalemia 55 0.120
43
c RHB024 Rhabdomyosarcoma 2 67 0.113
44
GLC003 Glucose Intolerance 54 0.113
45
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.100
46
P ALP004 Alport Syndrome 68 0.100
47
c FML001 Familial Atrial Fibrillation 65 0.100
48
HYP066 Hyperglycemia 61 0.100
49
P GLM007 Glomerulonephritis 57 0.100
50
P NRP001 Neuropathy 56 0.100
51
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.100
52
IMP005 Impotence 52 0.100
53
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.100
54
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.100
55
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.100
56
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.100
57
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.100
58
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.100
59
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.100
60
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.100
61
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.100
62
P RHM011 Rheumatoid Arthritis 80 0.093
63
c ATR087 Atrial Standstill 1 75 0.093
64
NTR005 Nutritional Deficiency Disease 62 0.093
65
c DBT099 Diabetes Mellitus, Type I 65 0.085
66
MSC007 Muscle Hypertrophy 64 0.085
67
P NPH012 Nephrotic Syndrome 60 0.085
68
PRT058 Pure Autonomic Failure 59 0.085
69
NPH010 Nephrosclerosis 50 0.085
70
IGG001 Iga Glomerulonephritis 48 0.085
71
P RNL015 Renal Hypertension 47 0.085
72
RNL077 Renal Fibrosis 47 0.085
73
C1N001 C1 Inhibitor Deficiency 39 0.085
74
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.085
75
c SYS001 Systemic Lupus Erythematosus 86 0.076
76
LPT014 Leptin Deficiency or Dysfunction 74 0.076
77
P TTR001 Tetralogy of Fallot 70 0.076
78
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.076
79
P PLY014 Polycystic Kidney Disease 62 0.076
80
ALL026 Allergic Hypersensitivity Disease 62 0.076
81
P LPS004 Lupus Erythematosus 61 0.076
82
P MYC008 Myocarditis 59 0.076
83
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.076
84
P EXN002 Exanthem 57 0.076
85
AGN016 Aging 56 0.076
86
INT007 Intermediate Coronary Syndrome 55 0.076
87
HYP060 Hyperinsulinism 54 0.076
88
P IGN003 Iga Nephropathy 1 49 0.076
89
SYS003 Systolic Heart Failure 49 0.076
90
LPT006 Leptin Receptor Deficiency 48 0.076
91
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.076
92
SYN036 Syncope 45 0.076
93
CVD001 Covid-19 44 0.076
94
49X006 49, Xxxxy Syndrome 41 0.076
95
c PLM022 Pulmonary Valve Insufficiency 39 0.076
96
c SYS043 Systemic Lupus Erythematosus 1 38 0.076
97
P GLM040 Glioma Susceptibility 1 81 0.065
98
c DLT002 Dilated Cardiomyopathy 79 0.065
99
GLB015 Glioblastoma Multiforme 75 0.065
100
BRN028 Brain Cancer 74 0.065
101
c HYP836 Hypercholesterolemia, Familial, 1 73 0.065
102
ANX010 Anxiety 73 0.065
103
MSC157 Muscular Dystrophy, Duchenne Type 72 0.065
104
DFC004 Deficiency Anemia 70 0.065
105
P MYP004 Myopathy 70 0.065
106
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.065
107
P ART022 Arthritis 69 0.065
108
P LVR013 Liver Disease 68 0.065
109
RCK004 Rickets 68 0.065
110
P CRD119 Cardiac Arrest 67 0.065
111
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.065
112
c MGR028 Migraine with or Without Aura 1 67 0.065
113
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.065
114
P MSC005 Muscular Dystrophy 66 0.065
115
MSC152 Muscular Dystrophy, Becker Type 63 0.065
116
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.065
117
P VSC011 Vasculitis 62 0.065
118
ATM095 Autoimmune Disease 62 0.065
119
LVR012 Liver Cirrhosis 62 0.065
120
c PNS012 Paine Syndrome 61 0.065
121
P OPT006 Optic Nerve Disease 60 0.065
122
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.065
123
CRD132 Cardiac Conduction Defect 58 0.065
124
P INF032 Infertility 57 0.065
125
P HDC001 Headache 57 0.065
126
THR024 Thrombosis 57 0.065
127
HYP266 Hypoxia 57 0.065
128
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.065
129
P MLN007 Male Infertility 55 0.065
130
RHM028 Rheumatic Heart Disease 53 0.065
131
STT041 Stuttering 52 0.065
132
P MTR003 Mitral Valve Stenosis 50 0.065
133
END021 Endomyocardial Fibrosis 49 0.065
134
URM002 Uremia 49 0.065
135
OLG001 Oligospermia 45 0.065
136
c PRM038 Primary Agammaglobulinemia 44 0.065
137
c SPR086 Spermatogenic Failure 3 44 0.065
138
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.065
139
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.065
140
c MYT029 Myotonia Congenita, Autosomal Recessive 41 0.065
141
GLC008 Glucose Metabolism Disease 40 0.065
142
48X005 48,xyyy 39 0.065
143
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.065
144
ATM052 Autoimmune Disease 1 37 0.065
145
MSC012 Muscular Dystrophy, Duchenne and Becker Type 34 0.065
146
CHL079 Children's Interstitial Lung Disease 26 0.065
147
P BRS047 Breast Cancer 97 0.053
148
P ALZ034 Alzheimer Disease 88 0.053
149
P CNR004 Cone-Rod Dystrophy 2 73 0.053
150
CNN005 Connective Tissue Disease 68 0.053
151
P HPT021 Hepatitis 67 0.053
152
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.053
153
P HYP069 Hyperparathyroidism 63 0.053
154
c GLY060 Glycogen Storage Disease Ia 63 0.053
155
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 62 0.053
156
LPD008 Lipid Metabolism Disorder 62 0.053
157
c HPT001 Hepatitis C 62 0.053
158
c SVR001 Severe Acute Respiratory Syndrome 62 0.053
159
P HYP750 Hypertriglyceridemia, Familial 62 0.053
160
CHL068 Cholestasis 61 0.053
161
P PNC044 Pancreatitis 61 0.053
162
GST033 Gestational Diabetes 61 0.053
163
P GLY013 Glycogen Storage Disease 60 0.053
164
c ACT071 Acute Kidney Failure 60 0.053
165
ANR040 Aneurysm 59 0.053
166
VSC002 Vascular Dementia 57 0.053
167
ATR057 Atrioventricular Block 55 0.053
168
PRC013 Pericarditis 54 0.053
169
P LCH002 Lichen Planus 53 0.053
170
c SCN007 Secondary Hyperparathyroidism 51 0.053
171
HYP081 Hypolipoproteinemia 51 0.053
172
c MTR002 Mitral Valve Insufficiency 48 0.053
173
HYP025 Hyperphosphatemia 48 0.053
174
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 47 0.053
175
P CRC039 Coarctation of Aorta 47 0.053
176
CRN019 Coronary Artery Vasospasm 46 0.053
177
CRB004 Cerebral Artery Occlusion 45 0.053
178
MSN001 Mesangial Proliferative Glomerulonephritis 45 0.053
179
ATN004 Autonomic Neuropathy 45 0.053
180
P RRC004 Rare Cardiomyopathy 44 0.053
181
c HYP272 Hypercholesterolemia, Familial, 3 44 0.053
182
CYT002 Cytokine Deficiency 42 0.053
183
HYP540 Hypertension, Diastolic 40 0.053
184
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.053
185
GLY081 Glycogen Storage Disease Due to Glucose-6-Phosphatase Deficiency 38 0.053
186
LCH013 Lichen Planus Pemphigoides 34 0.053
187
CRN270 Coronary Artery Dissection, Spontaneous 32 0.053
188
P CRT085 Carotid Intimal Medial Thickness 2 24 0.053
189
P HPT023 Hepatocellular Carcinoma 100 0.038
190
SCK003 Sickle Cell Anemia 74 0.038
191
P OST002 Osteoporosis 74 0.038
192
CRH001 Crohn's Disease 74 0.038
193
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.038
194
P PHC003 Pheochromocytoma 71 0.038
195
P HYP061 Hypertrophic Cardiomyopathy 70 0.038
196
PLM001 Pulmonary Tuberculosis 69 0.038
197
SVR097 Severe Cutaneous Adverse Reaction 69 0.038
198
P HYP086 Hypothyroidism 69 0.038
199
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.038
200
ART016 Aortic Aneurysm 69 0.038
201
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 68 0.038
202
BRN024 Bronchitis 68 0.038
203
P HYP098 Hypereosinophilic Syndrome 67 0.038
204
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.038
205
P DMN002 Dementia 66 0.038
206
HYP056 Hypoglycemia 66 0.038
207
KHL003 Kohlschutter-Tonz Syndrome 65 0.038
208
TTN003 Tetanus 65 0.038
209
c ART101 Aortic Valve Disease 2 65 0.038
210
c PRC016 Pre-Eclampsia 63 0.038
211
c ATM011 Autoimmune Hepatitis 63 0.038
212
P PSR002 Psoriasis 62 0.038
213
BLL006 Bullous Pemphigoid 62 0.038
214
P ORT004 Orthostatic Intolerance 62 0.038
215
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.038
216
PSR001 Psoriatic Arthritis 61 0.038
217
FTT001 Fatty Liver Disease 61 0.038
218
SPN186 Spinal Cord Injury 60 0.038
219
c ACT027 Acute Pancreatitis 60 0.038
220
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.038
221
c LTN004 Late-Onset Retinal Degeneration 59 0.038
222
ERY003 Erythema Multiforme 58 0.038
223
P MLT074 Multiple Endocrine Neoplasia 56 0.038
224
HMT008 Hematuria, Benign Familial 56 0.038
225
P PLY019 Polyneuropathy 56 0.038
226
c PRG126 Progressive Familial Heart Block 55 0.038
227
LMB062 Limb Ischemia 55 0.038
228
P DRR001 Diarrhea 55 0.038
229
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.038
230
P PMP001 Pemphigus 54 0.038
231
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.038
232
PLM010 Pulmonary Edema 54 0.038
233
NNL006 Non-Alcoholic Steatohepatitis 54 0.038
234
HRT012 Heart Valve Disease 53 0.038
235
PST011 Pustulosis of Palm and Sole 52 0.038
236
PNG002 Pain Agnosia 51 0.038
237
P LCT001 Lactic Acidosis 51 0.038
238
P ECL001 Eclampsia 50 0.038
239
P SCK005 Sickle Cell Disease 50 0.038
240
c PSR021 Psoriasis 14, Pustular 50 0.038
241
HYP006 Hypertensive Heart Disease 49 0.038
242
LFT001 Left Bundle Branch Hemiblock 49 0.038
243
P CMP008 Compartment Syndrome 49 0.038
244
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 48 0.038
245
P RNV001 Renovascular Hypertension 48 0.038
246
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.038
247
c HYD019 Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius 47 0.038
248
P CLL015 Collagen Disease 47 0.038
249
c ACT076 Acute Myocarditis 46 0.038
250
ADR040 Adrenal Gland Pheochromocytoma 46 0.038
251
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 46 0.038
252
DST006 Diastolic Heart Failure 45 0.038
253
GRN017 Granulocytopenia 44 0.038
254
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.038
255
SPR126 Superior Semicircular Canal Dehiscence 40 0.038
256
ANG049 Angioedema Induced by Ace Inhibitors 40 0.038
257
c HMG029 Hemoglobin Se Disease 39 0.038
258
P PRC031 Preeclampsia/eclampsia 1 38 0.038
259
SWL001 Swallowing Disorders 38 0.038
260
P PST059 Pustular Psoriasis 37 0.038
261
P FML187 Familial Hypertension 37 0.038
262
GLM044 Glomerular Disease 37 0.038
263
HYP114 Hypertensive Nephropathy 36 0.038
264
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.038
265
MCR119 Microtia, Hearing Impairment, and Cleft Palate 33 0.038
266
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.038
267
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.038
268
ERY066 Erythema Multiforme Major 30 0.038
269
EXF003 Exfoliative Dermatitis 27 0.038
270
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 0.038
271
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.038
272
SPR072 Superficial Pemphigus 17 0.038
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