Search results for Enalaprilat

218 hits were found for Enalaprilat

# Family MCID Name MIFTS Score
1
CNG034 Congestive Heart Failure 69 0.164
2
c HYP595 Hypertension, Essential 84 0.148
3
c ACT075 Acute Myocardial Infarction 57 0.108
4
c DLT002 Dilated Cardiomyopathy 79 0.100
5
ANG054 Angina Pectoris 66 0.100
6
c ATR087 Atrial Standstill 1 75 0.082
7
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.071
8
P KDN018 Kidney Disease 72 0.071
9
P DBT009 Diabetes Mellitus 64 0.071
10
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.071
11
P ANG015 Angioedema 57 0.071
12
c MCR113 Microvascular Complications of Diabetes 3 52 0.071
13
P RNV001 Renovascular Hypertension 48 0.071
14
c MCR120 Microvascular Complications of Diabetes 7 47 0.071
15
c MCR130 Microvascular Complications of Diabetes 6 41 0.071
16
c MCR133 Microvascular Complications of Diabetes 4 41 0.071
17
SNG003 Single Ventricular Heart 30 0.071
18
P RHM011 Rheumatoid Arthritis 80 0.058
19
P HRT032 Heart Disease 75 0.058
20
c THR092 Thrombophilia Due to Thrombin Defect 73 0.058
21
P CNR004 Cone-Rod Dystrophy 2 73 0.058
22
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.058
23
P NRB001 Neuroblastoma 72 0.058
24
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.058
25
P MCR115 Microvascular Complications of Diabetes 5 66 0.058
26
c MCR129 Microvascular Complications of Diabetes 1 66 0.058
27
ATH013 Atherosclerosis Susceptibility 65 0.058
28
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.058
29
LPP008 Lipoprotein Quantitative Trait Locus 62 0.058
30
TXC005 Toxic Shock Syndrome 62 0.058
31
SPN186 Spinal Cord Injury 60 0.058
32
P VNT002 Ventricular Septal Defect 60 0.058
33
PRT058 Pure Autonomic Failure 59 0.058
34
ISC004 Ischemia 58 0.058
35
HMR039 Hemorrhage, Intracerebral 57 0.058
36
PLM010 Pulmonary Edema 54 0.058
37
ART140 Arteries, Anomalies of 52 0.058
38
HRT011 Heart Septal Defect 50 0.058
39
QDR001 Quadriplegia 48 0.058
40
c MTR002 Mitral Valve Insufficiency 48 0.058
41
c MLG069 Malignant Hypertension 47 0.058
42
ACT003 Acute Kidney Tubular Necrosis 45 0.058
43
c ORT011 Orthostatic Hypotension 1 44 0.058
44
c MCR112 Microvascular Complications of Diabetes 2 41 0.058
45
C1N001 C1 Inhibitor Deficiency 39 0.058
46
48X005 48,xyyy 39 0.058
47
P LNG032 Lung Cancer 98 0.041
48
P BRS047 Breast Cancer 97 0.041
49
c SYS001 Systemic Lupus Erythematosus 86 0.041
50
MYL069 Myeloma, Multiple 85 0.041
51
c LKM061 Leukemia, Acute Myeloid 84 0.041
52
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.041
53
STR067 Stroke, Ischemic 81 0.041
54
INS024 Insulin-Like Growth Factor I 79 0.041
55
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.041
56
P RSP003 Respiratory Failure 74 0.041
57
SCK003 Sickle Cell Anemia 74 0.041
58
LPT014 Leptin Deficiency or Dysfunction 74 0.041
59
MSC157 Muscular Dystrophy, Duchenne Type 72 0.041
60
P FML011 Familial Adenomatous Polyposis 72 0.041
61
FBR012 Fabry Disease 72 0.041
62
PRP027 Peripheral Vascular Disease 71 0.041
63
P MYC007 Myocardial Infarction 70 0.041
64
DFC004 Deficiency Anemia 70 0.041
65
DWN001 Down Syndrome 70 0.041
66
P HYP061 Hypertrophic Cardiomyopathy 70 0.041
67
ADL002 Adult Syndrome 70 0.041
68
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.041
69
P MLN008 Melanoma 69 0.041
70
P ART022 Arthritis 69 0.041
71
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.041
72
P LKM062 Leukemia, Acute Lymphoblastic 69 0.041
73
P LYM118 Lymphoma 68 0.041
74
P PNM007 Pneumonia 68 0.041
75
P SYS005 Systemic Scleroderma 68 0.041
76
P LKM002 Leukemia 68 0.041
77
SKN019 Skin Melanoma 68 0.041
78
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 68 0.041
79
P ALP004 Alport Syndrome 68 0.041
80
P HPT021 Hepatitis 67 0.041
81
CRB039 Cerebrovascular Disease 67 0.041
82
P TRN020 Turner Syndrome 67 0.041
83
P PLM037 Pulmonary Hypertension 67 0.041
84
c RHB024 Rhabdomyosarcoma 2 67 0.041
85
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.041
86
ALC007 Alcohol Dependence 66 0.041
87
P DMN002 Dementia 66 0.041
88
P MSC005 Muscular Dystrophy 66 0.041
89
P ATR011 Atrial Fibrillation 66 0.041
90
CHG001 Chagas Disease 66 0.041
91
KHL003 Kohlschutter-Tonz Syndrome 65 0.041
92
c FML001 Familial Atrial Fibrillation 65 0.041
93
MSM014 Mismatch Repair Cancer Syndrome 65 0.041
94
BRR014 Barrett Esophagus 65 0.041
95
c DBT099 Diabetes Mellitus, Type I 65 0.041
96
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.041
97
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.041
98
MSC007 Muscle Hypertrophy 64 0.041
99
P ADN016 Adenocarcinoma 64 0.041
100
P GLM045 Glioma 63 0.041
101
c PRC016 Pre-Eclampsia 63 0.041
102
P VSC007 Vascular Disease 63 0.041
103
MSC152 Muscular Dystrophy, Becker Type 63 0.041
104
c SVR001 Severe Acute Respiratory Syndrome 62 0.041
105
ALL026 Allergic Hypersensitivity Disease 62 0.041
106
LVR012 Liver Cirrhosis 62 0.041
107
NTR005 Nutritional Deficiency Disease 62 0.041
108
HYP066 Hyperglycemia 61 0.041
109
DRM006 Dermatitis 61 0.041
110
P PNC044 Pancreatitis 61 0.041
111
P LPS004 Lupus Erythematosus 61 0.041
112
P MYL006 Myeloid Leukemia 60 0.041
113
c ACT027 Acute Pancreatitis 60 0.041
114
c ACT071 Acute Kidney Failure 60 0.041
115
PRT013 Portal Hypertension 59 0.041
116
c PSD114 Pseudohypoaldosteronism, Type I, Autosomal Recessive 59 0.041
117
P BRN022 Bronchiectasis 59 0.041
118
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.041
119
ANR040 Aneurysm 59 0.041
120
PPT005 Peptic Ulcer Disease 59 0.041
121
CRD132 Cardiac Conduction Defect 58 0.041
122
P ALC033 Alcohol Use Disorder 58 0.041
123
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.041
124
P GLM007 Glomerulonephritis 57 0.041
125
P EXN002 Exanthem 57 0.041
126
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.041
127
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.041
128
P CRD246 Cardiovascular System Disease 57 0.041
129
VSC002 Vascular Dementia 57 0.041
130
HMT008 Hematuria, Benign Familial 56 0.041
131
c INT072 Intestinal Pseudo-Obstruction 56 0.041
132
P NRP001 Neuropathy 56 0.041
133
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.041
134
AGN016 Aging 56 0.041
135
ATR057 Atrioventricular Block 55 0.041
136
c FML035 Familial Hyperlipidemia 55 0.041
137
c PRG126 Progressive Familial Heart Block 55 0.041
138
P ATR001 Atrioventricular Septal Defect 55 0.041
139
MMB001 Membranoproliferative Glomerulonephritis 55 0.041
140
INT007 Intermediate Coronary Syndrome 55 0.041
141
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.041
142
GLC003 Glucose Intolerance 54 0.041
143
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.041
144
AMN001 Amenorrhea 54 0.041
145
LYM040 Lymphoblastic Lymphoma 54 0.041
146
HRT012 Heart Valve Disease 53 0.041
147
P HMC002 Homocystinuria 53 0.041
148
PRP080 Peripheral Artery Disease 53 0.041
149
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.041
150
c CRS016 Crisponi/cold-Induced Sweating Syndrome 1 52 0.041
151
ACR041 Acromelic Frontonasal Dysostosis 52 0.041
152
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.041
153
P BRT004 Bartter Disease 52 0.041
154
IMP005 Impotence 52 0.041
155
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.041
156
PNG002 Pain Agnosia 51 0.041
157
OCL069 Ocular Motor Apraxia 51 0.041
158
PLS009 Plasma Cell Neoplasm 51 0.041
159
END086 End Stage Renal Disease 51 0.041
160
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.041
161
P ECL001 Eclampsia 50 0.041
162
P SCK005 Sickle Cell Disease 50 0.041
163
P IGN003 Iga Nephropathy 1 49 0.041
164
SYS003 Systolic Heart Failure 49 0.041
165
HYP006 Hypertensive Heart Disease 49 0.041
166
LFT001 Left Bundle Branch Hemiblock 49 0.041
167
END021 Endomyocardial Fibrosis 49 0.041
168
CCN002 Cocaine Abuse 49 0.041
169
URM002 Uremia 49 0.041
170
RGH001 Right Bundle Branch Block 48 0.041
171
IGG001 Iga Glomerulonephritis 48 0.041
172
LPT006 Leptin Receptor Deficiency 48 0.041
173
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.041
174
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.041
175
c HYD019 Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius 47 0.041
176
PRD004 Prediabetes Syndrome 47 0.041
177
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.041
178
LYM019 Lymphosarcoma 46 0.041
179
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.041
180
ATN005 Autonomic Dysfunction 46 0.041
181
HYP034 Hypertensive Encephalopathy 46 0.041
182
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.041
183
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.041
184
GLL048 Glial Tumor 45 0.041
185
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.041
186
URT010 Ureteral Obstruction 45 0.041
187
CYN002 Cyanosis, Transient Neonatal 45 0.041
188
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.041
189
DST006 Diastolic Heart Failure 45 0.041
190
C3G002 C3 Glomerulopathy 45 0.041
191
THR099 Third-Degree Atrioventricular Block 45 0.041
192
P END084 Endocrine System Disease 45 0.041
193
P PSD003 Pseudohypoaldosteronism 44 0.041
194
c PRM038 Primary Agammaglobulinemia 44 0.041
195
CVD001 Covid-19 44 0.041
196
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.041
197
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.041
198
IDP033 Idiopathic Edema 44 0.041
199
ELS006 Elsahy-Waters Syndrome 43 0.041
200
CYT002 Cytokine Deficiency 42 0.041
201
P PRT026 Parotitis 42 0.041
202
c MYT029 Myotonia Congenita, Autosomal Recessive 41 0.041
203
SPR126 Superior Semicircular Canal Dehiscence 40 0.041
204
ANG049 Angioedema Induced by Ace Inhibitors 40 0.041
205
HYP540 Hypertension, Diastolic 40 0.041
206
OCL010 Ocular Hypotension 39 0.041
207
c HMG029 Hemoglobin Se Disease 39 0.041
208
P PRC031 Preeclampsia/eclampsia 1 38 0.041
209
HYP264 Hypertonia 38 0.041
210
GLM044 Glomerular Disease 37 0.041
211
MSC012 Muscular Dystrophy, Duchenne and Becker Type 34 0.041
212
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.041
213
c RNL113 Renal Failure, Progressive, with Hypertension 34 0.041
214
c CHR064 Chronic Monocytic Leukemia 33 0.041
215
TXC020 Toxic Oil Syndrome 33 0.041
216
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.041
217
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.041
218
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.041
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