Search results for Lisinopril

296 hits were found for Lisinopril

# Family MCID Name MIFTS Score
1
c HYP595 Hypertension, Essential 84 0.525
2
CNG034 Congestive Heart Failure 69 0.334
3
P KDN018 Kidney Disease 72 0.229
4
P HRT032 Heart Disease 75 0.226
5
c MCR113 Microvascular Complications of Diabetes 3 52 0.220
6
c MCR120 Microvascular Complications of Diabetes 7 47 0.220
7
c MCR130 Microvascular Complications of Diabetes 6 41 0.220
8
c MCR133 Microvascular Complications of Diabetes 4 41 0.220
9
ADL002 Adult Syndrome 70 0.179
10
P MYC007 Myocardial Infarction 70 0.168
11
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.160
12
P MCR115 Microvascular Complications of Diabetes 5 66 0.160
13
P DBT009 Diabetes Mellitus 64 0.160
14
P ANG015 Angioedema 57 0.160
15
48X005 48,xyyy 39 0.155
16
c MCR129 Microvascular Complications of Diabetes 1 66 0.151
17
c MCR112 Microvascular Complications of Diabetes 2 41 0.142
18
P CRN300 Coronary Heart Disease 1 63 0.137
19
NTR005 Nutritional Deficiency Disease 62 0.137
20
P CRD246 Cardiovascular System Disease 57 0.137
21
STR067 Stroke, Ischemic 81 0.132
22
CRB039 Cerebrovascular Disease 67 0.132
23
MSC157 Muscular Dystrophy, Duchenne Type 72 0.127
24
P MSC005 Muscular Dystrophy 66 0.127
25
c DBT099 Diabetes Mellitus, Type I 65 0.127
26
LPP008 Lipoprotein Quantitative Trait Locus 62 0.127
27
P PNC044 Pancreatitis 61 0.127
28
c ATR087 Atrial Standstill 1 75 0.121
29
c RHB024 Rhabdomyosarcoma 2 67 0.121
30
P EXN002 Exanthem 57 0.121
31
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.116
32
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.116
33
c CHR684 Chronic Kidney Disease 70 0.116
34
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.116
35
ISC004 Ischemia 58 0.116
36
HYP540 Hypertension, Diastolic 40 0.116
37
P TRN020 Turner Syndrome 67 0.110
38
c ACT075 Acute Myocardial Infarction 57 0.110
39
MSC007 Muscle Hypertrophy 64 0.104
40
c ACT027 Acute Pancreatitis 60 0.104
41
END086 End Stage Renal Disease 51 0.104
42
P RNV001 Renovascular Hypertension 48 0.104
43
c HYP836 Hypercholesterolemia, Familial, 1 73 0.097
44
HYP005 Hypokalemia 55 0.097
45
ART140 Arteries, Anomalies of 52 0.097
46
c DLT002 Dilated Cardiomyopathy 79 0.090
47
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.090
48
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.090
49
P NPH012 Nephrotic Syndrome 60 0.090
50
P INF032 Infertility 57 0.090
51
P GLM007 Glomerulonephritis 57 0.090
52
GLC003 Glucose Intolerance 54 0.090
53
HYP081 Hypolipoproteinemia 51 0.090
54
OLG001 Oligospermia 45 0.090
55
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.082
56
PRP027 Peripheral Vascular Disease 71 0.082
57
P LYM118 Lymphoma 68 0.082
58
ATH013 Atherosclerosis Susceptibility 65 0.082
59
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.082
60
c ACT071 Acute Kidney Failure 60 0.082
61
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.082
62
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.082
63
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.082
64
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.082
65
HYP006 Hypertensive Heart Disease 49 0.082
66
BRN071 Brain Injury 49 0.082
67
IGG001 Iga Glomerulonephritis 48 0.082
68
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.082
69
P RNL015 Renal Hypertension 47 0.082
70
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.082
71
LYM019 Lymphosarcoma 46 0.082
72
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.082
73
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.082
74
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.082
75
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.082
76
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.082
77
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.082
78
ATX019 Ataxia with Vitamin E Deficiency 42 0.082
79
P PLM037 Pulmonary Hypertension 67 0.073
80
P ATR011 Atrial Fibrillation 66 0.073
81
LPD008 Lipid Metabolism Disorder 62 0.073
82
P PLY014 Polycystic Kidney Disease 62 0.073
83
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.073
84
P FCL005 Focal Segmental Glomerulosclerosis 57 0.073
85
P NRP001 Neuropathy 56 0.073
86
MCL006 Macular Retinal Edema 55 0.073
87
P MLN007 Male Infertility 55 0.073
88
P LNG032 Lung Cancer 98 0.063
89
P BRS047 Breast Cancer 97 0.063
90
IMM167 Immune Deficiency Disease 78 0.063
91
LPT014 Leptin Deficiency or Dysfunction 74 0.063
92
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.063
93
HMN044 Human Immunodeficiency Virus Type 1 71 0.063
94
P MYP004 Myopathy 70 0.063
95
P OCL013 Oculodentodigital Dysplasia 69 0.063
96
c HYP768 Hyperlipoproteinemia, Type I 67 0.063
97
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.063
98
ALC007 Alcohol Dependence 66 0.063
99
P DMN002 Dementia 66 0.063
100
c SML038 Small Cell Cancer of the Lung 65 0.063
101
KHL003 Kohlschutter-Tonz Syndrome 65 0.063
102
c FML001 Familial Atrial Fibrillation 65 0.063
103
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.063
104
P ADL010 Adult Respiratory Distress Syndrome 65 0.063
105
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.063
106
c MSC036 Muscular Dystrophy-Dystroglycanopathy , Type C, 5 64 0.063
107
P VSC007 Vascular Disease 63 0.063
108
TRN015 Transient Cerebral Ischemia 63 0.063
109
ACQ007 Acquired Immunodeficiency Syndrome 60 0.063
110
P OPT006 Optic Nerve Disease 60 0.063
111
PRT058 Pure Autonomic Failure 59 0.063
112
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.063
113
EYD002 Eye Disease 58 0.063
114
EPD050 Epidermolysis Bullosa Simplex with Muscular Dystrophy 56 0.063
115
AGN016 Aging 56 0.063
116
P DRR001 Diarrhea 55 0.063
117
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.063
118
P PMP001 Pemphigus 54 0.063
119
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.063
120
GST037 Gastroparesis 54 0.063
121
PLM010 Pulmonary Edema 54 0.063
122
DBT010 Diabetic Neuropathy 54 0.063
123
P LMB006 Limb-Girdle Muscular Dystrophy 53 0.063
124
PRP080 Peripheral Artery Disease 53 0.063
125
P RTN018 Retinal Disease 53 0.063
126
LNG031 Lung Benign Neoplasm 51 0.063
127
AZS001 Azoospermia 50 0.063
128
DYS073 Dysphagia 50 0.063
129
SYS003 Systolic Heart Failure 49 0.063
130
47X002 47,xyy 49 0.063
131
c MTR002 Mitral Valve Insufficiency 48 0.063
132
c FML253 Familial Cold Autoinflammatory Syndrome 3 47 0.063
133
c HYP272 Hypercholesterolemia, Familial, 3 44 0.063
134
c ORT011 Orthostatic Hypotension 1 44 0.063
135
IDP033 Idiopathic Edema 44 0.063
136
GST020 Gastric Antral Vascular Ectasia 41 0.063
137
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.063
138
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.063
139
OST012 Osteoarthritis 78 0.052
140
KPS004 Kaposi Sarcoma 75 0.052
141
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.052
142
c THR092 Thrombophilia Due to Thrombin Defect 73 0.052
143
P MLT020 Multiple Sclerosis 72 0.052
144
DWN001 Down Syndrome 70 0.052
145
P HYP086 Hypothyroidism 69 0.052
146
P LKM062 Leukemia, Acute Lymphoblastic 69 0.052
147
P LVR013 Liver Disease 68 0.052
148
P PNM007 Pneumonia 68 0.052
149
P LKM002 Leukemia 68 0.052
150
P HPT021 Hepatitis 67 0.052
151
c MGR028 Migraine with or Without Aura 1 67 0.052
152
ANG054 Angina Pectoris 66 0.052
153
P PLM036 Pulmonary Fibrosis 65 0.052
154
SRC014 Sarcoma 65 0.052
155
P HYP069 Hyperparathyroidism 63 0.052
156
c FNC043 Fanconi Anemia, Complementation Group E 62 0.052
157
P HYP750 Hypertriglyceridemia, Familial 62 0.052
158
BLL006 Bullous Pemphigoid 62 0.052
159
P VSC011 Vasculitis 62 0.052
160
LVR012 Liver Cirrhosis 62 0.052
161
HYP066 Hyperglycemia 61 0.052
162
OST003 Osteonecrosis 61 0.052
163
c PNS012 Paine Syndrome 61 0.052
164
P ENC018 Encephalopathy 61 0.052
165
PRT013 Portal Hypertension 59 0.052
166
c PRM005 Primary Hyperparathyroidism 58 0.052
167
THR024 Thrombosis 57 0.052
168
VSC002 Vascular Dementia 57 0.052
169
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.052
170
HYP060 Hyperinsulinism 54 0.052
171
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.052
172
LYM040 Lymphoblastic Lymphoma 54 0.052
173
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.052
174
SPN035 Spindle Cell Sarcoma 53 0.052
175
P MMB011 Membranous Nephropathy 50 0.052
176
MTB004 Metabolic Acidosis 50 0.052
177
NPH010 Nephrosclerosis 50 0.052
178
ASP007 Aspiration Pneumonia 48 0.052
179
RNL077 Renal Fibrosis 47 0.052
180
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.052
181
c FCL025 Focal Segmental Glomerulosclerosis 1 46 0.052
182
URT010 Ureteral Obstruction 45 0.052
183
ASP008 Aspiration Pneumonitis 45 0.052
184
HRT015 Heritable Pulmonary Arterial Hypertension 44 0.052
185
c PRM038 Primary Agammaglobulinemia 44 0.052
186
P RPD001 Rapidly Progressive Glomerulonephritis 44 0.052
187
CRS001 Crescentic Glomerulonephritis 43 0.052
188
NSP002 Nasopharyngitis 43 0.052
189
PMP004 Pemphigus Foliaceus 43 0.052
190
TRP009 Triple X Syndrome 42 0.052
191
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.052
192
49X006 49, Xxxxy Syndrome 41 0.052
193
ALC005 Alcoholic Pancreatitis 40 0.052
194
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.052
195
SWL001 Swallowing Disorders 38 0.052
196
ACT228 Acute Radiation Syndrome 29 0.052
197
CHL079 Children's Interstitial Lung Disease 26 0.052
198
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 0.052
199
P RHM011 Rheumatoid Arthritis 80 0.037
200
AST005 Asthma 76 0.037
201
P RSP003 Respiratory Failure 74 0.037
202
SCK003 Sickle Cell Anemia 74 0.037
203
ANX010 Anxiety 73 0.037
204
DFC004 Deficiency Anemia 70 0.037
205
P ART022 Arthritis 69 0.037
206
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.037
207
GST092 Gastroesophageal Reflux 67 0.037
208
P CRD119 Cardiac Arrest 67 0.037
209
P HYP098 Hypereosinophilic Syndrome 67 0.037
210
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.037
211
HYP056 Hypoglycemia 66 0.037
212
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.037
213
PRT036 Peritonitis 64 0.037
214
P PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 64 0.037
215
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.037
216
P HML002 Hemolytic Anemia 63 0.037
217
SKN016 Skin Disease 63 0.037
218
c SVR001 Severe Acute Respiratory Syndrome 62 0.037
219
P ESP024 Esophagitis 62 0.037
220
HSH003 Hashimoto Thyroiditis 62 0.037
221
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.037
222
FTT001 Fatty Liver Disease 61 0.037
223
P LPS004 Lupus Erythematosus 61 0.037
224
LNG099 Lung Disease 60 0.037
225
P MYC008 Myocarditis 59 0.037
226
PLM033 Pulmonary Embolism 59 0.037
227
PRN019 Perinatal Necrotizing Enterocolitis 59 0.037
228
P ALC033 Alcohol Use Disorder 58 0.037
229
P URT039 Urticaria 58 0.037
230
P PRP019 Peripheral Nervous System Disease 58 0.037
231
P HDC001 Headache 57 0.037
232
P BPL003 Bipolar Disorder 56 0.037
233
P PLY011 Polycystic Ovary Syndrome 56 0.037
234
GNR004 Generalized Anxiety Disorder 56 0.037
235
P GST044 Gastritis 56 0.037
236
c FML035 Familial Hyperlipidemia 55 0.037
237
c PRG126 Progressive Familial Heart Block 55 0.037
238
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.037
239
INT007 Intermediate Coronary Syndrome 55 0.037
240
PRP030 Purpura 54 0.037
241
TRD006 Tardive Dyskinesia 54 0.037
242
P ALP008 Alopecia 54 0.037
243
P CYS039 Cystic Kidney Disease 54 0.037
244
P ART021 Arteriosclerosis 54 0.037
245
P TRM003 Tremor 54 0.037
246
PRS045 Prostatic Hypertrophy 53 0.037
247
OST016 Osteochondrosis 53 0.037
248
P THY032 Thyroiditis 52 0.037
249
HYP014 Hyperuricemia 52 0.037
250
PPT001 Peptic Esophagitis 52 0.037
251
PNG002 Pain Agnosia 51 0.037
252
OCL069 Ocular Motor Apraxia 51 0.037
253
PRS021 Prostatic Adenoma 51 0.037
254
ENT011 Enterocolitis 51 0.037
255
BHR001 Behr Syndrome 51 0.037
256
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.037
257
P SCK005 Sickle Cell Disease 50 0.037
258
LNG015 Lingual-Facial-Buccal Dyskinesia 50 0.037
259
P IGN003 Iga Nephropathy 1 49 0.037
260
LFT001 Left Bundle Branch Hemiblock 49 0.037
261
PRS129 Prostatic Hyperplasia, Benign 49 0.037
262
CHL004 Cholelithiasis 49 0.037
263
URM002 Uremia 49 0.037
264
c BCT013 Bacterial Pneumonia 48 0.037
265
HYP043 Hyperandrogenism 48 0.037
266
FBR032 Fibromuscular Dysplasia 48 0.037
267
SXL003 Sexual Disorder 47 0.037
268
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.037
269
c MLG069 Malignant Hypertension 47 0.037
270
P BLR006 Biliary Tract Disease 47 0.037
271
RTN001 Retinal Vasculitis 47 0.037
272
c ACT076 Acute Myocarditis 46 0.037
273
HYP034 Hypertensive Encephalopathy 46 0.037
274
DST006 Diastolic Heart Failure 45 0.037
275
MCR037 Macroglossia 45 0.037
276
P END084 Endocrine System Disease 45 0.037
277
SBC016 Subacute Delirium 44 0.037
278
CRB008 Cerebral Atherosclerosis 44 0.037
279
PTY001 Pityriasis Rosea 44 0.037
280
CVD001 Covid-19 44 0.037
281
PLY068 Polysubstance Abuse 43 0.037
282
BCK006 Back Pain 42 0.037
283
c MJR024 Major Affective Disorder 9 41 0.037
284
RDN001 Reading Disorder 40 0.037
285
ANG049 Angioedema Induced by Ace Inhibitors 40 0.037
286
c MJR022 Major Affective Disorder 8 38 0.037
287
P FML187 Familial Hypertension 37 0.037
288
c ATM022 Autoimmune Myocarditis 35 0.037
289
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.037
290
P CRN133 Coronary Artery Disease, Autosomal Dominant, 1 32 0.037
291
SLW005 Slowed Nerve Conduction Velocity, Autosomal Dominant 32 0.037
292
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.037
293
PRK005 Prekallikrein Deficiency 29 0.037
294
PST092 Posttransplant Acute Limbic Encephalitis 29 0.037
295
c BNG021 Benign Essential Hypertension 26 0.037
296
INT074 Intracranial Arteriosclerosis 23 0.037
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