Search results for Losartan

530 hits were found for Losartan

# Family MCID Name MIFTS Score
1
c HYP595 Hypertension, Essential 84 0.674
2
HYP005 Hypokalemia 55 0.402
3
P KDN018 Kidney Disease 72 0.360
4
c MCR113 Microvascular Complications of Diabetes 3 52 0.353
5
c MCR120 Microvascular Complications of Diabetes 7 47 0.337
6
c MCR130 Microvascular Complications of Diabetes 6 41 0.337
7
c MCR133 Microvascular Complications of Diabetes 4 41 0.337
8
CNG034 Congestive Heart Failure 69 0.290
9
c CHR684 Chronic Kidney Disease 70 0.263
10
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.259
11
P HRT032 Heart Disease 75 0.246
12
END086 End Stage Renal Disease 51 0.246
13
MRF001 Marfan Syndrome 77 0.219
14
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.209
15
P CRD246 Cardiovascular System Disease 57 0.186
16
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.179
17
STR067 Stroke, Ischemic 81 0.176
18
CRB039 Cerebrovascular Disease 67 0.176
19
MSC007 Muscle Hypertrophy 64 0.176
20
P DBT009 Diabetes Mellitus 64 0.174
21
c ACT075 Acute Myocardial Infarction 57 0.167
22
P MCR115 Microvascular Complications of Diabetes 5 66 0.161
23
c MCR129 Microvascular Complications of Diabetes 1 66 0.161
24
P MYC007 Myocardial Infarction 70 0.159
25
ADL002 Adult Syndrome 70 0.159
26
P VSC007 Vascular Disease 63 0.153
27
c MCR112 Microvascular Complications of Diabetes 2 41 0.153
28
48X005 48,xyyy 39 0.151
29
P GLM007 Glomerulonephritis 57 0.148
30
HYP014 Hyperuricemia 52 0.148
31
c ATR087 Atrial Standstill 1 75 0.142
32
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.142
33
LPD008 Lipid Metabolism Disorder 62 0.142
34
IGG001 Iga Glomerulonephritis 48 0.139
35
HYP066 Hyperglycemia 61 0.136
36
P ANG015 Angioedema 57 0.136
37
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.136
38
c RHB024 Rhabdomyosarcoma 2 67 0.133
39
P CRN300 Coronary Heart Disease 1 63 0.133
40
FTT001 Fatty Liver Disease 61 0.133
41
LPP008 Lipoprotein Quantitative Trait Locus 62 0.130
42
LVR012 Liver Cirrhosis 62 0.130
43
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.126
44
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.126
45
P LVR013 Liver Disease 68 0.123
46
P PLM037 Pulmonary Hypertension 67 0.123
47
c ACT071 Acute Kidney Failure 60 0.123
48
ISC004 Ischemia 58 0.123
49
NNL006 Non-Alcoholic Steatohepatitis 54 0.123
50
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.120
51
ART016 Aortic Aneurysm 69 0.120
52
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.120
53
PRT013 Portal Hypertension 59 0.120
54
CRD132 Cardiac Conduction Defect 58 0.120
55
MRD002 Marden-Walker Syndrome 56 0.120
56
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.116
57
P ATR011 Atrial Fibrillation 66 0.116
58
ATH013 Atherosclerosis Susceptibility 65 0.116
59
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.116
60
ART074 Aortic Dissection 52 0.116
61
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.116
62
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.116
63
RNL077 Renal Fibrosis 47 0.116
64
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.116
65
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.116
66
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.116
67
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.116
68
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.116
69
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.116
70
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.116
71
P MSC005 Muscular Dystrophy 66 0.112
72
P PLM036 Pulmonary Fibrosis 65 0.112
73
P HYP061 Hypertrophic Cardiomyopathy 70 0.108
74
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.108
75
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.108
76
ART140 Arteries, Anomalies of 52 0.108
77
ATX019 Ataxia with Vitamin E Deficiency 42 0.108
78
P PNC035 Pancreatic Cancer 84 0.105
79
GLC003 Glucose Intolerance 54 0.105
80
P RNV001 Renovascular Hypertension 48 0.105
81
CVD001 Covid-19 44 0.105
82
c HYP836 Hypercholesterolemia, Familial, 1 73 0.100
83
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.100
84
P TRN020 Turner Syndrome 67 0.100
85
NTR005 Nutritional Deficiency Disease 62 0.100
86
P IGN003 Iga Nephropathy 1 49 0.100
87
c DLT002 Dilated Cardiomyopathy 79 0.096
88
P SLP006 Sleep Apnea 69 0.096
89
CNN005 Connective Tissue Disease 68 0.096
90
c DBT099 Diabetes Mellitus, Type I 65 0.096
91
ANR040 Aneurysm 59 0.096
92
HYP060 Hyperinsulinism 54 0.096
93
URM002 Uremia 49 0.096
94
MSC157 Muscular Dystrophy, Duchenne Type 72 0.092
95
DFC004 Deficiency Anemia 70 0.092
96
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.092
97
c SVR001 Severe Acute Respiratory Syndrome 62 0.092
98
c MTR002 Mitral Valve Insufficiency 48 0.092
99
SCK003 Sickle Cell Anemia 74 0.087
100
PRP027 Peripheral Vascular Disease 71 0.087
101
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 68 0.087
102
GT001 Gout 64 0.087
103
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.087
104
URT010 Ureteral Obstruction 45 0.087
105
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.087
106
P FML187 Familial Hypertension 37 0.087
107
CYT018 Cytochrome P450 2d6 Variant 27 0.087
108
CYS001 Cystic Fibrosis 81 0.082
109
ANX010 Anxiety 73 0.082
110
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.082
111
P ADL010 Adult Respiratory Distress Syndrome 65 0.082
112
IDP011 Idiopathic Interstitial Pneumonia 59 0.082
113
PRT058 Pure Autonomic Failure 59 0.082
114
P EXN002 Exanthem 57 0.082
115
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.082
116
c FML035 Familial Hyperlipidemia 55 0.082
117
P RNL015 Renal Hypertension 47 0.082
118
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.077
119
HMN044 Human Immunodeficiency Virus Type 1 71 0.077
120
P SYS005 Systemic Scleroderma 68 0.077
121
BRN024 Bronchitis 68 0.077
122
PNC129 Pancreatic Adenocarcinoma 68 0.077
123
ANG054 Angina Pectoris 66 0.077
124
P ADN016 Adenocarcinoma 64 0.077
125
P ORT004 Orthostatic Intolerance 62 0.077
126
P PNC044 Pancreatitis 61 0.077
127
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.077
128
c ACT027 Acute Pancreatitis 60 0.077
129
NWB001 Newborn Respiratory Distress Syndrome 58 0.077
130
P FCL005 Focal Segmental Glomerulosclerosis 57 0.077
131
HYP266 Hypoxia 57 0.077
132
P NRP001 Neuropathy 56 0.077
133
IMP005 Impotence 52 0.077
134
P SCK005 Sickle Cell Disease 50 0.077
135
P ART018 Aortic Valve Insufficiency 49 0.077
136
c PRM038 Primary Agammaglobulinemia 44 0.077
137
SPR126 Superior Semicircular Canal Dehiscence 40 0.077
138
c HMG029 Hemoglobin Se Disease 39 0.077
139
P LNG032 Lung Cancer 98 0.071
140
LPT014 Leptin Deficiency or Dysfunction 74 0.071
141
c ART101 Aortic Valve Disease 2 65 0.071
142
P NPH012 Nephrotic Syndrome 60 0.071
143
LNG099 Lung Disease 60 0.071
144
AGN016 Aging 56 0.071
145
PRP080 Peripheral Artery Disease 53 0.071
146
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.071
147
ACT029 Acute Interstitial Pneumonia 49 0.071
148
CYT002 Cytokine Deficiency 42 0.071
149
c CHR682 Chronic Bilirubin Encephalopathy 39 0.071
150
GLM044 Glomerular Disease 37 0.071
151
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.071
152
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.065
153
c ART115 Aortic Valve Disease 1 75 0.065
154
P RSP003 Respiratory Failure 74 0.065
155
c THR092 Thrombophilia Due to Thrombin Defect 73 0.065
156
P PNM007 Pneumonia 68 0.065
157
c SML038 Small Cell Cancer of the Lung 65 0.065
158
APN008 Apnea, Obstructive Sleep 64 0.065
159
c ALP101 Alpha-Thalassemia 62 0.065
160
P HYP750 Hypertriglyceridemia, Familial 62 0.065
161
P ESP024 Esophagitis 62 0.065
162
ALL026 Allergic Hypersensitivity Disease 62 0.065
163
VRL011 Viral Infectious Disease 61 0.065
164
STT001 Status Epilepticus 60 0.065
165
P THL005 Thalassemia 60 0.065
166
PST028 Post-Traumatic Stress Disorder 58 0.065
167
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.065
168
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.065
169
P ESP035 Esophagitis, Eosinophilic, 1 57 0.065
170
THR024 Thrombosis 57 0.065
171
NPH009 Nephrolithiasis 55 0.065
172
P PLM034 Pulmonary Emphysema 55 0.065
173
ESN005 Eosinophilic Gastroenteritis 55 0.065
175
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.065
176
c MLG069 Malignant Hypertension 47 0.065
177
ACT084 Acute Stress Disorder 47 0.065
178
RYN005 Raynaud Phenomenon 47 0.065
179
IDP033 Idiopathic Edema 44 0.065
180
PLM068 Pulmonary Vein Stenosis 39 0.065
181
P VSC018 Visceral Steatosis 33 0.065
182
RSP007 Respiratory Distress Syndrome, Infant 30 0.065
183
P GLM040 Glioma Susceptibility 1 81 0.058
184
GLB015 Glioblastoma Multiforme 75 0.058
185
CRH001 Crohn's Disease 74 0.058
186
P AMY004 Amyloidosis 70 0.058
187
DWN001 Down Syndrome 70 0.058
188
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.058
189
P DMN002 Dementia 66 0.058
190
KHL003 Kohlschutter-Tonz Syndrome 65 0.058
191
c FML001 Familial Atrial Fibrillation 65 0.058
192
PRT036 Peritonitis 64 0.058
193
DPR016 Depression 63 0.058
194
c HPT001 Hepatitis C 62 0.058
195
P PLY014 Polycystic Kidney Disease 62 0.058
196
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.058
197
ACQ007 Acquired Immunodeficiency Syndrome 60 0.058
198
P MYC008 Myocarditis 59 0.058
199
P CMR001 Camurati-Engelmann Disease 59 0.058
200
VSL002 Visual Epilepsy 59 0.058
201
P PRP019 Peripheral Nervous System Disease 58 0.058
202
P SZR006 Seizure Disorder 56 0.058
203
c MCR256 Microphthalmia, Syndromic 9 56 0.058
204
P SCK002 Sick Sinus Syndrome 55 0.058
205
INT007 Intermediate Coronary Syndrome 55 0.058
206
CRT017 Cartilage Disease 54 0.058
207
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.058
208
HYP081 Hypolipoproteinemia 51 0.058
209
P MMB011 Membranous Nephropathy 50 0.058
210
ART017 Aortic Disease 49 0.058
211
LPT006 Leptin Receptor Deficiency 48 0.058
212
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.058
213
PRD004 Prediabetes Syndrome 47 0.058
214
SYN036 Syncope 45 0.058
215
HYP540 Hypertension, Diastolic 40 0.058
216
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.058
217
P ALZ034 Alzheimer Disease 88 0.050
218
c SYS001 Systemic Lupus Erythematosus 86 0.050
219
CNN003 Conn's Syndrome 79 0.050
220
OST012 Osteoarthritis 78 0.050
221
BRN028 Brain Cancer 74 0.050
222
MLT157 Multiple System Atrophy 1 70 0.050
223
P TTR001 Tetralogy of Fallot 70 0.050
224
P ALP004 Alport Syndrome 68 0.050
225
c MCP052 Mucopolysaccharidosis, Type Vi 67 0.050
226
P HPT021 Hepatitis 67 0.050
227
PSY004 Psychotic Disorder 67 0.050
228
OST159 Osteogenic Sarcoma 66 0.050
229
SPN209 Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations 66 0.050
231
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.050
232
c PRC016 Pre-Eclampsia 63 0.050
233
CLT003 Colitis 62 0.050
234
P PSR002 Psoriasis 62 0.050
235
c HPT003 Hepatitis a 62 0.050
236
P VSC011 Vasculitis 62 0.050
237
MSS001 Masa Syndrome 62 0.050
238
c MCP047 Mucopolysaccharidosis, Type Iva 61 0.050
239
c SCL052 Scleroderma, Familial Progressive 61 0.050
240
P LPS004 Lupus Erythematosus 61 0.050
241
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.050
242
INT066 Interstitial Lung Disease 60 0.050
243
P BND020 Bone Disease 59 0.050
244
P BCL017 B-Cell Lymphoma 58 0.050
245
P MLT007 Multiple Epiphyseal Dysplasia 58 0.050
246
P ALC033 Alcohol Use Disorder 58 0.050
247
DSS008 Disease of Mental Health 58 0.050
248
c MCP004 Mucopolysaccharidosis Iv 57 0.050
249
VSC002 Vascular Dementia 57 0.050
250
P URF003 Urofacial Syndrome 1 57 0.050
251
MCL006 Macular Retinal Edema 55 0.050
252
URN010 Urinary Tract Obstruction 55 0.050
253
MSC162 Muscular Dystrophy, Congenital Merosin-Deficient, 1a 54 0.050
254
PLM010 Pulmonary Edema 54 0.050
255
ALC009 Alcoholic Liver Cirrhosis 53 0.050
256
PST011 Pustulosis of Palm and Sole 52 0.050
257
LNG031 Lung Benign Neoplasm 51 0.050
258
CHR515 Chronic Atrial and Intestinal Dysrhythmia 50 0.050
259
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.050
260
HYP006 Hypertensive Heart Disease 49 0.050
261
SNT005 Sinoatrial Node Disease 49 0.050
262
BNR002 Bone Resorption Disease 48 0.050
263
DBT006 Diabetic Macular Edema 48 0.050
264
URN009 Urinary System Disease 48 0.050
265
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 46 0.050
266
c FCL025 Focal Segmental Glomerulosclerosis 1 46 0.050
267
PST048 Postural Orthostatic Tachycardia Syndrome 45 0.050
268
CRB004 Cerebral Artery Occlusion 45 0.050
269
OBS082 Obstructive Nephropathy 42 0.050
270
LWR018 Lower Urinary Tract Obstruction, Congenital 40 0.050
271
SKL017 Skeletal Dysplasias 40 0.050
272
C1N001 C1 Inhibitor Deficiency 39 0.050
273
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.050
274
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.050
275
MCP033 Mucopolysaccharidoses 38 0.050
276
P MRQ003 Morquio Syndrome 37 0.050
277
c RNL113 Renal Failure, Progressive, with Hypertension 34 0.050
279
P BRS047 Breast Cancer 97 0.041
281
IMM167 Immune Deficiency Disease 78 0.041
282
P SCH015 Schizophrenia 74 0.041
283
ULC004 Ulcerative Colitis 73 0.041
284
FBR012 Fabry Disease 72 0.041
285
P EPL164 Epilepsy 71 0.041
286
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 0.041
287
P MLN008 Melanoma 69 0.041
288
SKN019 Skin Melanoma 68 0.041
289
P MJR001 Major Depressive Disorder 68 0.041
290
c INF071 Inflammatory Bowel Disease 1 67 0.041
291
ALC007 Alcohol Dependence 66 0.041
292
PRT037 Pertussis 65 0.041
293
P HRP006 Herpes Simplex 65 0.041
294
P HRM001 Hermansky-Pudlak Syndrome 64 0.041
295
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.041
296
PRP083 Porphyria, Acute Intermittent 64 0.041
297
TRN015 Transient Cerebral Ischemia 63 0.041
298
c FNC043 Fanconi Anemia, Complementation Group E 62 0.041
299
P PRP029 Porphyria 62 0.041
300
CHR066 Chronic Fatigue Syndrome 61 0.041
301
VRC005 Varicose Veins 60 0.041
302
P OCL002 Oculocutaneous Albinism 60 0.041
303
MNT002 Mental Depression 58 0.041
304
CNS004 Constipation 58 0.041
305
P UVT001 Uveitis 57 0.041
306
P HDC001 Headache 57 0.041
307
CPR004 Coproporphyria, Hereditary 57 0.041
308
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.041
309
CYT008 Cytomegalovirus Infection 57 0.041
310
P BPL003 Bipolar Disorder 56 0.041
311
SCH003 Schizophreniform Disorder 56 0.041
312
PRP082 Porphyria, Congenital Erythropoietic 56 0.041
313
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.041
314
P HYP076 Hyperthyroidism 55 0.041
315
END040 Endogenous Depression 55 0.041
316
PRP030 Purpura 54 0.041
317
P TRM003 Tremor 54 0.041
318
HRT012 Heart Valve Disease 53 0.041
319
CRH005 Crohn's Colitis 53 0.041
320
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.041
321
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 53 0.041
322
P HML001 Hemolytic-Uremic Syndrome 53 0.041
323
c HRM017 Hermansky-Pudlak Syndrome 2 53 0.041
324
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.041
325
NRT001 Neurotic Disorder 53 0.041
326
P LMB006 Limb-Girdle Muscular Dystrophy 53 0.041
327
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.041
328
ACR041 Acromelic Frontonasal Dysostosis 52 0.041
329
P MSC003 Muscular Atrophy 52 0.041
330
OLG003 Oligohydramnios 51 0.041
331
c HRM005 Hermansky-Pudlak Syndrome 1 51 0.041
332
HYP781 Hypoascorbemia 51 0.041
333
c ACT078 Acute Porphyria 51 0.041
334
SCH012 Schizoaffective Disorder 50 0.041
335
CRT013 Carotid Stenosis 50 0.041
336
P TMP001 Temporal Lobe Epilepsy 50 0.041
337
c AMY009 Amyloidosis Aa 50 0.041
338
MTB004 Metabolic Acidosis 50 0.041
339
SYS003 Systolic Heart Failure 49 0.041
340
47X002 47,xyy 49 0.041
341
ATS010 Autosomal Recessive Disease 48 0.041
342
HYP025 Hyperphosphatemia 48 0.041
343
P PRP056 Porphyria, Acute Hepatic 48 0.041
344
SXL003 Sexual Disorder 47 0.041
345
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.041
346
c HRM008 Hermansky-Pudlak Syndrome 5 47 0.041
347
STR089 Storage Pool Platelet Disease 47 0.041
348
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.041
349
P CRC039 Coarctation of Aorta 47 0.041
350
ALB002 Albinism 46 0.041
351
c HRM007 Hermansky-Pudlak Syndrome 4 46 0.041
352
ANR004 Anuria 46 0.041
353
c HRM009 Hermansky-Pudlak Syndrome 6 45 0.041
354
c CNT015 Central Sleep Apnea 45 0.041
355
MSN001 Mesangial Proliferative Glomerulonephritis 45 0.041
356
ATN004 Autonomic Neuropathy 45 0.041
357
c HRM006 Hermansky-Pudlak Syndrome 3 44 0.041
358
P HYP761 Hypouricemia, Renal, 1 44 0.041
359
c HYP272 Hypercholesterolemia, Familial, 3 44 0.041
360
c HRM012 Hermansky-Pudlak Syndrome 9 43 0.041
361
P MJR007 Major Affective Disorder 1 43 0.041
362
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.041
363
GST020 Gastric Antral Vascular Ectasia 41 0.041
364
c MJR024 Major Affective Disorder 9 41 0.041
365
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 0.041
366
RDN001 Reading Disorder 40 0.041
367
c PLM022 Pulmonary Valve Insufficiency 39 0.041
368
c MJR022 Major Affective Disorder 8 38 0.041
369
CTN011 Cutaneous Porphyria 38 0.041
370
c HRM010 Hermansky-Pudlak Syndrome 7 37 0.041
371
c HRM011 Hermansky-Pudlak Syndrome 8 35 0.041
372
c MJR008 Major Affective Disorder 2 35 0.041
373
P ANT001 Anterolateral Myocardial Infarction 34 0.041
374
c MJR023 Major Affective Disorder 7 33 0.041
375
c MJR003 Major Affective Disorder 6 33 0.041
376
c MJR006 Major Affective Disorder 5 33 0.041
377
KDN013 Kidney Hypertrophy 32 0.041
378
FNT004 Fainting 30 0.041
379
c MJR004 Major Affective Disorder 4 28 0.041
380
CHL079 Children's Interstitial Lung Disease 26 0.041
381
MST020 Mast Cell Activation Syndrome 26 0.041
382
c CHR344 Chronic Orthostatic Intolerance 17 0.041
383
P CLR023 Colorectal Cancer 99 0.029
384
P PRS040 Prostate Cancer 97 0.029
385
P OVR042 Ovarian Cancer 88 0.029
386
P RHM011 Rheumatoid Arthritis 80 0.029
387
INS024 Insulin-Like Growth Factor I 79 0.029
388
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.029
389
ADR007 Adrenoleukodystrophy 75 0.029
390
END057 Endometrial Cancer 74 0.029
391
P OST002 Osteoporosis 74 0.029
392
P NRB001 Neuroblastoma 72 0.029
393
P MYP004 Myopathy 70 0.029
394
P ART022 Arthritis 69 0.029
395
SVR097 Severe Cutaneous Adverse Reaction 69 0.029
396
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.029
397
P LKM002 Leukemia 68 0.029
398
RCK004 Rickets 68 0.029
399
P THR014 Thrombocytopenia 67 0.029
400
GST092 Gastroesophageal Reflux 67 0.029
401
c MGR028 Migraine with or Without Aura 1 67 0.029
402
P CLC063 Celiac Disease 1 66 0.029
403
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.029
404
HYP056 Hypoglycemia 66 0.029
405
IRR002 Irritable Bowel Syndrome 65 0.029
406
KWS002 Kawasaki Disease 65 0.029
407
P PRD008 Periodontitis 64 0.029
408
P HYP069 Hyperparathyroidism 63 0.029
409
P END044 Endometriosis 63 0.029
410
c GLC092 Glaucoma, Primary Open Angle 62 0.029
411
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.029
412
c LCL006 Localized Scleroderma 62 0.029
413
c BRN108 Branchiootic Syndrome 1 62 0.029
414
BLL006 Bullous Pemphigoid 62 0.029
415
P ART023 Arthropathy 62 0.029
416
MDD011 Mood Disorder 62 0.029
417
P PRM006 Primary Biliary Cirrhosis 62 0.029
419
INT002 Intermittent Claudication 61 0.029
420
c WLM018 Wilms Tumor 5 61 0.029
421
P MYL006 Myeloid Leukemia 60 0.029
422
HPT019 Hepatic Encephalopathy 60 0.029
423
c MSC170 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 2 60 0.029
424
P CTR002 Cataract 60 0.029
425
HYD002 Hydronephrosis 60 0.029
426
PLM033 Pulmonary Embolism 59 0.029
427
PRG009 Progressive Multifocal Leukoencephalopathy 59 0.029
428
c LTN004 Late-Onset Retinal Degeneration 59 0.029
429
P DNG005 Dengue Virus 59 0.029
430
P ANP001 Anaplastic Large Cell Lymphoma 58 0.029
431
P INT070 Intestinal Obstruction 58 0.029
432
CNT047 Contact Dermatitis 58 0.029
433
ERY003 Erythema Multiforme 58 0.029
434
P URT039 Urticaria 58 0.029
435
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.029
436
P EHL001 Ehlers-Danlos Syndrome 58 0.029
437
c DWL002 Dowling-Degos Disease 1 58 0.029
438
PMP006 Pemphigus Vulgaris, Familial 57 0.029
439
IRN002 Iron Metabolism Disease 57 0.029
440
P RHN004 Rhinitis 57 0.029
441
P PYL005 Pyelonephritis 56 0.029
442
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.029
443
ADR008 Adrenal Adenoma 55 0.029
444
P PMP001 Pemphigus 54 0.029
445
AMN003 Amnestic Disorder 54 0.029
446
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 0.029
447
P INF037 Inflammatory Bowel Disease 54 0.029
448
ANL018 Analbuminemia 54 0.029
449
P ART021 Arteriosclerosis 54 0.029
450
DBT010 Diabetic Neuropathy 54 0.029
451
STF002 Stiff Skin Syndrome 54 0.029
452
RCS002 Recessive Dystrophic Epidermolysis Bullosa 54 0.029
453
PRS045 Prostatic Hypertrophy 53 0.029
454
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.029
455
P EPD016 Epidermolysis Bullosa 53 0.029
456
RHM028 Rheumatic Heart Disease 53 0.029
457
INT075 Intracranial Hypertension 53 0.029
458
IRD001 Iridocyclitis 53 0.029
459
c EPD076 Epidermolysis Bullosa Dystrophica, Autosomal Recessive 52 0.029
460
P DDN001 Duodenal Ulcer 52 0.029
461
P ACT105 Acute Mountain Sickness 52 0.029
462
PNG002 Pain Agnosia 51 0.029
463
PRS021 Prostatic Adenoma 51 0.029
464
KRT009 Keratosis 51 0.029
465
ESP002 Esophageal Varix 51 0.029
466
TRM010 Traumatic Brain Injury 51 0.029
467
P THR015 Thrombophilia 51 0.029
468
P OVR082 Overgrowth Syndrome 50 0.029
469
RSP006 Respiratory System Disease 50 0.029
470
NPH010 Nephrosclerosis 50 0.029
471
ENT004 Enthesopathy 49 0.029
472
DFF035 Diffuse Cutaneous Systemic Sclerosis 49 0.029
473
VRC001 Varicocele 49 0.029
474
LFT001 Left Bundle Branch Hemiblock 49 0.029
475
P OPN001 Open-Angle Glaucoma 49 0.029
476
BRN071 Brain Injury 49 0.029
477
WTH001 Withdrawal Disorder 48 0.029
478
HPT009 Hepatopulmonary Syndrome 48 0.029
479
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.029
480
HYP068 Hyperostosis 48 0.029
481
END062 Endometrial Hyperplasia 48 0.029
482
FBR032 Fibromuscular Dysplasia 48 0.029
483
ART004 Aortic Atherosclerosis 47 0.029
484
CRN017 Coronary Thrombosis 47 0.029
485
c ACT076 Acute Myocarditis 46 0.029
486
c KNB006 Knobloch Syndrome 1 46 0.029
487
RTN020 Retinal Vascular Disease 46 0.029
488
GNR003 Generalized Atherosclerosis 46 0.029
489
MYC005 Myocardial Stunning 46 0.029
490
c ACT042 Acute Pyelonephritis 46 0.029
491
CNT025 Central Pontine Myelinolysis 46 0.029
492
HPT004 Hepatic Coma 45 0.029
493
ACT003 Acute Kidney Tubular Necrosis 45 0.029
494
P GLP001 Geleophysic Dysplasia 44 0.029
495
NSP002 Nasopharyngitis 43 0.029
496
MYH012 Myhre Syndrome 43 0.029
497
HYP457 Hypertrophic Scars 42 0.029
498
c RTN047 Retinitis Pigmentosa 18 42 0.029
499
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.029
500
DRG024 Drug Allergy 42 0.029
501
RST023 Resting Heart Rate, Variation in 41 0.029
502
DBT002 Diabetic Autonomic Neuropathy 41 0.029
503
DFF003 Diffuse Scleroderma 41 0.029
504
ANG049 Angioedema Induced by Ace Inhibitors 40 0.029
505
KLD004 Keloid Disorder 40 0.029
506
CRN020 Coronary Restenosis 39 0.029
507
HYP008 Hypertensive Retinopathy 39 0.029
508
ALD013 Aldosterone-Producing Adenoma 39 0.029
509
DBT007 Diabetic Cataract 38 0.029
510
TYM001 Tympanosclerosis 38 0.029
511
HRT036 Heritable Thoracic Aortic Disease 35 0.029
512
RFR013 Refractory Celiac Disease 35 0.029
513
PRM329 Premature Aging 35 0.029
514
NNT039 Neonatal Marfan Syndrome 34 0.029
515
PLT015 Platelet Aggregation, Spontaneous 34 0.029
516
MCR119 Microtia, Hearing Impairment, and Cleft Palate 33 0.029
517
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.029
518
P KNB001 Knobloch Syndrome 32 0.029
519
ERY066 Erythema Multiforme Major 30 0.029
520
TLG001 Telogen Effluvium 30 0.029
521
P SKL032 Skeletal Muscle Disease 29 0.029
522
c TYP028 Type 1 Diabetes Mellitus 2 28 0.029
523
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.029
524
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.029
525
ETH012 Ethylene Glycol Poisoning 26 0.029
526
CRR012 Cirrhotic Cardiomyopathy 24 0.029
527
DPS001 Dipsogenic Diabetes Insipidus 23 0.029
528
ATR024 Atrial Fibrillation and Stroke 22 0.029
529
c CMR006 Camurati-Engelmann Disease, Type 2 21 0.029
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