Search results for Esomeprazole

314 hits were found for Esomeprazole

# Family MCID Name MIFTS Score
1
GST092 Gastroesophageal Reflux 68 0.652
2
P ESP024 Esophagitis 62 0.521
3
PPT001 Peptic Esophagitis 47 0.417
4
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.415
5
PPT005 Peptic Ulcer Disease 60 0.354
6
HLC007 Helicobacter Pylori Infection 61 0.331
7
DYS014 Dyspepsia 51 0.299
8
P DDN001 Duodenal Ulcer 50 0.292
9
PRP027 Peripheral Vascular Disease 72 0.246
10
P GST044 Gastritis 58 0.243
11
GST023 Gastric Ulcer 53 0.235
12
BRR014 Barrett Esophagus 67 0.208
13
P BLD124 Bleeding Disorder, Platelet-Type, 11 66 0.192
14
ADL002 Adult Syndrome 62 0.185
15
GST050 Gastrointestinal System Disease 57 0.181
16
ACT058 Active Peptic Ulcer Disease 55 0.178
17
P ART022 Arthritis 71 0.166
18
ALL026 Allergic Hypersensitivity Disease 65 0.158
19
c RHB024 Rhabdomyosarcoma 2 64 0.150
20
DYS073 Dysphagia 52 0.150
21
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.150
22
OST012 Osteoarthritis 80 0.141
23
c PRC016 Pre-Eclampsia 63 0.141
24
AST005 Asthma 80 0.136
25
HYP005 Hypokalemia 55 0.136
26
P GST053 Gastric Cancer 85 0.131
27
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.131
28
ISC004 Ischemia 62 0.131
29
ZLL002 Zollinger-Ellison Syndrome 54 0.131
30
P CRN018 Coronary Artery Anomaly 67 0.126
31
P ATR005 Atrophic Gastritis 49 0.126
32
P ECL001 Eclampsia 53 0.120
33
ATX019 Ataxia with Vitamin E Deficiency 46 0.120
34
P PRC031 Preeclampsia/eclampsia 1 42 0.115
35
P CLR023 Colorectal Cancer 100 0.109
36
c HYP595 Hypertension, Essential 87 0.109
37
P RHM011 Rheumatoid Arthritis 82 0.109
38
P PNM007 Pneumonia 71 0.109
39
c PNS012 Paine Syndrome 61 0.109
40
P DRR001 Diarrhea 55 0.109
41
48X005 48,xyyy 37 0.109
42
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.103
43
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.103
44
P KDN018 Kidney Disease 73 0.103
45
P TRN020 Turner Syndrome 66 0.103
46
LNG099 Lung Disease 62 0.103
47
ART140 Arteries, Anomalies of 60 0.103
48
P CRN300 Coronary Heart Disease 1 59 0.103
49
P ESP035 Esophagitis, Eosinophilic, 1 54 0.103
50
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.103
51
ESP021 Esophageal Cancer 90 0.096
52
CNS004 Constipation 59 0.096
53
STM006 Stomach Disease 50 0.096
54
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.089
55
ANX010 Anxiety 75 0.089
56
LVR012 Liver Cirrhosis 67 0.089
57
HYP266 Hypoxia 58 0.089
58
P LRY019 Laryngitis 53 0.089
59
PNG002 Pain Agnosia 52 0.089
60
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.089
61
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.089
62
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.089
63
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.089
64
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.089
65
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.089
66
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.089
67
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.089
68
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.089
69
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.089
70
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.089
71
ESN014 Eosinophilic Enteropathy 34 0.089
72
P BRS047 Breast Cancer 99 0.081
73
P HRT032 Heart Disease 78 0.081
74
P MYC007 Myocardial Infarction 74 0.081
75
c SPN225 Spondyloarthropathy 1 74 0.081
76
P LVR013 Liver Disease 71 0.081
77
DWN001 Down Syndrome 70 0.081
78
P LYM118 Lymphoma 70 0.081
79
CNG034 Congestive Heart Failure 69 0.081
80
c JVN010 Juvenile Rheumatoid Arthritis 67 0.081
81
IRR002 Irritable Bowel Syndrome 65 0.081
82
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.081
83
c ACT075 Acute Myocardial Infarction 59 0.081
84
P INF037 Inflammatory Bowel Disease 57 0.081
85
c LRG017 Large Intestine Cancer 53 0.081
86
SPN051 Spondylitis 53 0.081
87
LYM019 Lymphosarcoma 48 0.081
88
PNC085 Penicillin Allergy 44 0.081
89
INF009 Inflammatory Spondylopathy 29 0.081
90
CYS001 Cystic Fibrosis 84 0.073
91
STR067 Stroke, Ischemic 82 0.073
92
P OST002 Osteoporosis 79 0.073
93
GST019 Gastrointestinal Stromal Tumor 76 0.073
94
PLM001 Pulmonary Tuberculosis 72 0.073
95
LPT014 Leptin Deficiency or Dysfunction 72 0.073
96
CRB039 Cerebrovascular Disease 71 0.073
97
P MYC084 Mycobacterium Tuberculosis 1 69 0.073
98
c CHR684 Chronic Kidney Disease 68 0.073
99
P HYP098 Hypereosinophilic Syndrome 67 0.073
100
P PLM036 Pulmonary Fibrosis 66 0.073
101
P VSC007 Vascular Disease 65 0.073
102
P ADN016 Adenocarcinoma 65 0.073
103
IDP011 Idiopathic Interstitial Pneumonia 65 0.073
104
IGR001 Ige Responsiveness, Atopic 61 0.073
105
c ACT071 Acute Kidney Failure 60 0.073
106
END030 End Stage Renal Failure 60 0.073
107
P RHN004 Rhinitis 59 0.073
108
P SZR006 Seizure Disorder 59 0.073
109
VSL002 Visual Epilepsy 58 0.073
110
P ALC033 Alcohol Use Disorder 58 0.073
111
BCT022 Bacterial Infectious Disease 57 0.073
112
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.073
113
CMR002 Coumarin Resistance 56 0.073
114
P ANG015 Angioedema 54 0.073
115
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 54 0.073
116
PRG017 Paraganglioma and Gastric Stromal Sarcoma 52 0.073
117
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.073
118
PNC034 Pancreas Disease 51 0.073
119
c PNC106 Pancreatic Agenesis 1 50 0.073
120
c RHM021 Rheumatoid Arthritis, Systemic Juvenile 49 0.073
121
PLR007 Pleural Empyema 44 0.073
122
PLY068 Polysubstance Abuse 44 0.073
123
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.073
124
ASP030 Aspirin Resistance 42 0.073
125
DYS011 Dyskinesia of Esophagus 42 0.073
126
CLP006 Clopidogrel Resistance 41 0.073
127
49X002 49,xxxxy Syndrome 39 0.073
128
CHL079 Children's Interstitial Lung Disease 27 0.073
129
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.063
130
SQM013 Squamous Cell Carcinoma, Head and Neck 81 0.063
131
c PLM164 Pulmonary Hypertension, Primary, 1 79 0.063
132
P SCH015 Schizophrenia 76 0.063
133
P CNR004 Cone-Rod Dystrophy 2 72 0.063
134
RCK004 Rickets 70 0.063
135
c ATS007 Autism Spectrum Disorder 69 0.063
136
P PLM037 Pulmonary Hypertension 69 0.063
137
ALL003 Allergic Rhinitis 69 0.063
138
P ATS364 Autism 68 0.063
139
P THR014 Thrombocytopenia 67 0.063
140
P DBT009 Diabetes Mellitus 66 0.063
141
DSS008 Disease of Mental Health 66 0.063
142
P OCL013 Oculodentodigital Dysplasia 65 0.063
143
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.063
144
TXC005 Toxic Shock Syndrome 63 0.063
145
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.063
146
ATM095 Autoimmune Disease 62 0.063
147
P ART023 Arthropathy 61 0.063
148
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.063
149
SQM006 Squamous Cell Carcinoma 60 0.063
150
P HDC001 Headache 59 0.063
151
P PRV006 Pervasive Developmental Disorder 58 0.063
152
P EXN002 Exanthem 58 0.063
153
CMM005 Common Cold 57 0.063
154
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.063
155
GNR004 Generalized Anxiety Disorder 55 0.063
156
BRN038 Bronchial Disease 53 0.063
157
OCL069 Ocular Motor Apraxia 53 0.063
158
FDL002 Food Allergy 52 0.063
159
GST037 Gastroparesis 52 0.063
160
P CHR345 Chronic Pain 52 0.063
161
P THR015 Thrombophilia 51 0.063
162
HYP081 Hypolipoproteinemia 51 0.063
163
BNR002 Bone Resorption Disease 51 0.063
164
APL002 Aplasia of Lacrimal and Salivary Glands 51 0.063
165
URM002 Uremia 50 0.063
166
ACH005 Achalasia 50 0.063
167
MTN003 Motion Sickness 48 0.063
168
BHR001 Behr Syndrome 47 0.063
169
MGS001 Megaesophagus 47 0.063
170
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.063
171
HRT015 Heritable Pulmonary Arterial Hypertension 46 0.063
172
IDP035 Idiopathic Achalasia 46 0.063
173
INT067 Interstitial Nephritis 46 0.063
174
DDN006 Duodenitis 44 0.063
175
GST030 Gastrinoma 43 0.063
176
ACH015 Achalasia, Familial Esophageal 42 0.063
177
SWL001 Swallowing Disorders 39 0.063
178
VSM001 Vasomotor Rhinitis 36 0.063
179
RRS014 Rare Surgical Neurologic Disease 33 0.063
180
LYM015 Lymphocytic Gastritis 32 0.063
181
TTH007 Tooth Erosion 32 0.063
182
CYT018 Cytochrome P450 2d6 Variant 28 0.063
183
NNH013 Non-Histaminic Angioedema 26 0.063
184
c RRH030 Rare Headache 16 0.063
185
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.051
186
P MLT020 Multiple Sclerosis 73 0.051
187
BRN024 Bronchitis 70 0.051
188
P HYP086 Hypothyroidism 70 0.051
189
c PNC108 Pancreatitis, Hereditary 70 0.051
190
P HPT021 Hepatitis 69 0.051
191
P MJR001 Major Depressive Disorder 69 0.051
192
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.051
193
P ASP006 Aspergillosis 67 0.051
194
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.051
195
DPR016 Depression 64 0.051
196
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 63 0.051
197
DRM006 Dermatitis 63 0.051
198
P PSR002 Psoriasis 63 0.051
199
P LPS004 Lupus Erythematosus 62 0.051
200
P PNC044 Pancreatitis 61 0.051
201
FBR047 Fibromyalgia 60 0.051
202
MNT002 Mental Depression 60 0.051
203
GST045 Gastroenteritis 60 0.051
204
EYD002 Eye Disease 59 0.051
205
P SJG008 Sjogren Syndrome 57 0.051
206
RLP002 Relapsing-Remitting Multiple Sclerosis 57 0.051
207
RHM027 Rheumatic Disease 56 0.051
208
END040 Endogenous Depression 55 0.051
209
ESP023 Esophageal Disease 55 0.051
210
c PSR017 Psoriasis 2 55 0.051
211
MRG003 Marginal Zone B-Cell Lymphoma 55 0.051
212
EXP004 Exophthalmos 53 0.051
213
KRT006 Keratoconjunctivitis 53 0.051
214
THY030 Thyroid Gland Disease 53 0.051
215
KRT001 Keratoconjunctivitis Sicca 53 0.051
216
NRT001 Neurotic Disorder 53 0.051
217
PST011 Pustulosis of Palm and Sole 51 0.051
218
c PSR023 Psoriasis 1 50 0.051
219
DRY001 Dry Eye Syndrome 50 0.051
220
P CTN003 Cutaneous Lupus Erythematosus 50 0.051
221
PYL006 Pyloric Stenosis 47 0.051
222
LPT006 Leptin Receptor Deficiency 47 0.051
223
LRY017 Laryngeal Disease 47 0.051
224
CYT002 Cytokine Deficiency 46 0.051
225
RDN001 Reading Disorder 42 0.051
226
c PSR028 Psoriasis 7 40 0.051
227
c PSR018 Psoriasis 13 40 0.051
228
c PSR032 Psoriasis 11 40 0.051
229
MYF002 Myofascial Pain Syndrome 39 0.051
230
C1N001 C1 Inhibitor Deficiency 39 0.051
231
ORB013 Orbital Disease 38 0.051
232
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.051
233
NDL024 Nodal Marginal Zone Lymphoma 37 0.051
234
RTN145 Retinal Arterial Macroaneurysm with Supravalvular Pulmonic Stenosis 34 0.051
235
c SBC035 Subacute Cutaneous Lupus Erythematosus 34 0.051
236
DFC004 Deficiency Anemia 77 0.036
237
P PRK057 Parkinson Disease, Late-Onset 77 0.036
238
P RSP003 Respiratory Failure 75 0.036
239
c HYP836 Hypercholesterolemia, Familial, 1 74 0.036
240
c MLT156 Multiple Endocrine Neoplasia, Type I 71 0.036
241
LYM133 Lymphoma, Hodgkin, Classic 70 0.036
242
P DMN002 Dementia 68 0.036
243
ALC007 Alcohol Dependence 68 0.036
244
HYP056 Hypoglycemia 68 0.036
245
P LKM062 Leukemia, Acute Lymphoblastic 68 0.036
246
ATH013 Atherosclerosis Susceptibility 68 0.036
247
c FML021 Familial Hypercholesterolemia 67 0.036
248
SVR097 Severe Cutaneous Adverse Reaction 66 0.036
249
c FNC043 Fanconi Anemia, Complementation Group E 64 0.036
250
LPD008 Lipid Metabolism Disorder 64 0.036
251
KHL003 Kohlschutter-Tonz Syndrome 63 0.036
252
CLT003 Colitis 63 0.036
253
PPL049 Papillon-Lefevre Syndrome 63 0.036
254
CRD223 Cardiac Arrhythmia 61 0.036
255
INT066 Interstitial Lung Disease 61 0.036
256
VRC005 Varicose Veins 61 0.036
257
THR100 Thrombocytopenic Purpura, Autoimmune 61 0.036
258
P CRD132 Cardiac Conduction Defect 61 0.036
259
P MLT074 Multiple Endocrine Neoplasia 59 0.036
260
NRN004 Neuroendocrine Tumor 59 0.036
261
c ACT210 Acute Respiratory Distress Syndrome 59 0.036
262
IRN001 Iron Deficiency Anemia 59 0.036
263
IRN002 Iron Metabolism Disease 58 0.036
264
THR024 Thrombosis 58 0.036
265
INT007 Intermediate Coronary Syndrome 58 0.036
266
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.036
267
BRN056 Bronchopulmonary Dysplasia 57 0.036
268
INT030 Intracranial Aneurysm 57 0.036
269
ERY003 Erythema Multiforme 57 0.036
270
APH002 Aphasia 56 0.036
271
PRP030 Purpura 56 0.036
272
P LYM031 Lymphocytic Leukemia 56 0.036
273
ATR057 Atrioventricular Block 56 0.036
274
PHR003 Pharyngitis 56 0.036
275
P INT068 Intestinal Disease 56 0.036
276
HRT012 Heart Valve Disease 56 0.036
277
CYS010 Cystinosis 55 0.036
278
c GRV008 Graves Disease 1 55 0.036
279
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 54 0.036
280
TRM010 Traumatic Brain Injury 54 0.036
281
INT075 Intracranial Hypertension 54 0.036
282
c ACT134 Acute Liver Failure 53 0.036
283
MYM001 Myoma 52 0.036
284
c INH020 Inherited Metabolic Disorder 51 0.036
285
OVR082 Overgrowth Syndrome 51 0.036
286
P ANL018 Analbuminemia 51 0.036
287
BRN071 Brain Injury 51 0.036
288
ENT011 Enterocolitis 51 0.036
289
GLS018 Glass Syndrome 51 0.036
290
SXL003 Sexual Disorder 49 0.036
291
GST027 Gastric Lymphoma 49 0.036
292
VTM033 Vitamin K Deficiency Bleeding 47 0.036
293
MCR191 Microscopic Colitis 47 0.036
294
TRC003 Trichomoniasis 46 0.036
295
PRS063 Paresthesia 46 0.036
296
SYN036 Syncope 46 0.036
297
ASP007 Aspiration Pneumonia 46 0.036
298
GLC096 Galactorrhea 44 0.036
299
c HYP272 Hypercholesterolemia, Familial, 3 44 0.036
300
MCR011 Microinvasive Gastric Cancer 43 0.036
301
CLL021 Collagenous Colitis 42 0.036
302
ANG049 Angioedema Induced by Ace Inhibitors 41 0.036
303
THR099 Third-Degree Atrioventricular Block 39 0.036
304
BLR002 Bile Reflux 38 0.036
305
FXD003 Fixed Drug Eruption 36 0.036
306
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 36 0.036
307
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 33 0.036
308
PHT004 Photoallergic Dermatitis 33 0.036
309
c DRR009 Diarrhea 6 32 0.036
310
SPN011 Spongiotic Dermatitis 30 0.036
311
ERY066 Erythema Multiforme Major 29 0.036
312
EXF003 Exfoliative Dermatitis 28 0.036
313
CRD220 Cardiac Valvular Defect, Developmental 27 0.036
314
c CHR465 Chronic Diarrhea Due to Guanylate Cyclase 2c Overactivity 21 0.036
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