Search results for atorvastatin

653 hits were found for atorvastatin

# Family MCID Name MIFTS Score
1
LPD008 Lipid Metabolism Disorder 65 0.619
2
c CRN018 Coronary Artery Anomaly 74 0.476
3
c CRN300 Coronary Heart Disease 1 62 0.475
4
ISC006 Ischemic Heart Disease 72 0.457
5
ISC004 Ischemia 67 0.434
6
ART140 Arteries, Anomalies of 67 0.392
7
c ART021 Arteriosclerosis 61 0.367
8
c HRT032 Heart Disease 76 0.359
9
c MYC007 Myocardial Infarction 78 0.358
10
c DBT009 Diabetes Mellitus 67 0.306
11
c CRD246 Cardiovascular System Disease 57 0.296
12
c DBT026 Diabetes Mellitus, Noninsulin-Dependent 92 0.291
13
VSC007 Vascular Disease 72 0.289
14
c KDN018 Kidney Disease 71 0.252
15
GLC008 Glucose Metabolism Disease 54 0.230
16
c HYP607 Hypercholesterolemia, Familial 82 0.227
17
ANG054 Angina Pectoris 70 0.221
19
URN009 Urinary System Disease 59 0.193
20
CRB039 Cerebrovascular Disease 70 0.186
21
CNG034 Congestive Heart Failure 71 0.184
22
P ACT075 Acute Myocardial Infarction 57 0.183
23
ATM095 Autoimmune Disease 68 0.175
24
THR024 Thrombosis 64 0.173
25
P CHR089 Chronic Kidney Failure 73 0.171
26
c ATR011 Atrial Fibrillation 69 0.161
27
ACQ007 Acquired Immunodeficiency Syndrome 66 0.161
28
HMN014 Human Immunodeficiency Virus Infectious Disease 62 0.161
29
c MYP004 Myopathy 65 0.159
30
OCL033 Oculocerebral Syndrome with Hypopigmentation 46 0.155
31
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 53 0.153
32
P TRC078 Trichohepatoenteric Syndrome 2 35 0.153
33
INT007 Intermediate Coronary Syndrome 50 0.151
34
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 35 0.151
35
c LVR013 Liver Disease 77 0.148
36
c PRD008 Periodontitis 66 0.144
37
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 58 0.144
38
SPS003 Spastic Diplegia 49 0.144
39
IMM136 Immune System Disease 57 0.141
40
c HYP614 Hyperlipidemia, Familial Combined 56 0.139
41
c MSC033 Muscle Disorders 56 0.139
42
c PRS040 Prostate Cancer 93 0.137
43
STR067 Stroke, Ischemic 84 0.134
44
P PRD040 Periodontitis, Chronic 60 0.134
45
HYP060 Hyperinsulinism 57 0.134
46
SKN027 Skin Conditions 51 0.134
47
c ART022 Arthritis 78 0.132
48
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.129
49
SKN016 Skin Disease 68 0.127
50
TRN015 Transient Cerebral Ischemia 59 0.127
51
MSC190 Muscular Disease 55 0.124
52
MSC004 Muscle Tissue Disease 39 0.124
53
c MLT020 Multiple Sclerosis 76 0.121
54
c NRV007 Nervous System Disease 72 0.118
55
ALL026 Allergic Hypersensitivity Disease 68 0.118
56
c ENC018 Encephalopathy 65 0.118
57
VRL011 Viral Infectious Disease 69 0.116
58
CRT016 Carotid Artery Disease 58 0.116
59
P HYP595 Hypertension, Essential 77 0.110
60
c HPT021 Hepatitis 74 0.110
61
c OST002 Osteoporosis 74 0.110
62
c DBT085 Diabetes Mellitus, Insulin-Dependent 73 0.110
63
PRD007 Periodontal Disease 66 0.110
64
MTH009 Mouth Disease 66 0.110
65
P CNT035 Central Nervous System Disease 65 0.110
66
c BRS047 Breast Cancer 100 0.107
67
c ALZ034 Alzheimer Disease 88 0.107
68
c RHM011 Rheumatoid Arthritis 82 0.107
69
AST005 Asthma 81 0.107
70
PRP027 Peripheral Vascular Disease 72 0.107
71
CNN005 Connective Tissue Disease 67 0.107
72
RHM027 Rheumatic Disease 65 0.107
73
P THR001 Thrombocytopenia Due to Platelet Alloimmunization 61 0.107
74
c CLL015 Collagen Disease 52 0.107
75
P HNT011 Huntington Disease-Like 3 40 0.107
76
c GRF003 Graft-Versus-Host Disease 72 0.103
77
c LPS004 Lupus Erythematosus 69 0.103
78
c ART023 Arthropathy 68 0.103
79
THR100 Thrombocytopenic Purpura, Autoimmune 68 0.103
80
BRS051 Breast Disease 68 0.103
81
FTT001 Fatty Liver Disease 66 0.103
82
c CRD119 Cardiac Arrest 66 0.103
83
JNT002 Joint Disorders 64 0.103
84
c HMR003 Hemorrhagic Disease 59 0.103
85
P ACT135 Acute Graft Versus Host Disease 58 0.103
86
LYM024 Lymphatic System Disease 55 0.103
87
c BLD051 Blood Coagulation Disease 51 0.103
88
c RTN008 Retinitis Pigmentosa 79 0.100
89
HMN044 Human Immunodeficiency Virus Type 1 75 0.100
90
c LKM002 Leukemia 72 0.100
91
LNG099 Lung Disease 70 0.100
92
c NNL004 Nonalcoholic Fatty Liver Disease 56 0.100
93
PRP080 Peripheral Artery Disease 56 0.100
94
P HNT004 Huntington Disease-Like 2 48 0.100
95
ART016 Aortic Aneurysm 71 0.097
96
DMN002 Dementia 69 0.097
97
P HPT003 Hepatitis a 66 0.097
98
RSP006 Respiratory System Disease 64 0.097
99
HMT018 Hematopoietic Stem Cell Transplantation 59 0.097
100
NNL002 Nonalcoholic Steatohepatitis 55 0.097
101
P SYS001 Systemic Lupus Erythematosus 88 0.093
102
c INF038 Influenza 75 0.093
103
GST050 Gastrointestinal System Disease 67 0.093
104
ERY003 Erythema Multiforme 63 0.093
105
c HYP750 Hypertriglyceridemia, Familial 58 0.093
106
P ACT071 Acute Kidney Failure 54 0.093
107
CLC006 Calcinosis 53 0.093
108
MNS002 Mini Stroke 25 0.093
109
HML018 Homologous Wasting Disease 25 0.093
110
c PNM007 Pneumonia 72 0.089
111
c ADN016 Adenocarcinoma 71 0.089
112
P ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 67 0.089
113
c LYM033 Lymphoproliferative Syndrome 63 0.089
114
DMY004 Demyelinating Disease 60 0.089
115
SLP005 Sleep Disorder 60 0.089
116
CRT013 Carotid Stenosis 52 0.089
117
P MTR002 Mitral Valve Insufficiency 50 0.089
118
DST081 Distal Trisomy 11q 20 0.089
119
P THR092 Thrombophilia Due to Thrombin Defect 70 0.086
120
c LYM118 Lymphoma 69 0.086
121
c PSR002 Psoriasis 67 0.086
122
BND020 Bone Disease 65 0.086
123
HYP066 Hyperglycemia 65 0.086
124
P FTT008 Fatty Liver Disease, Nonalcoholic 1 61 0.086
125
ATH013 Atherosclerosis Susceptibility 61 0.086
126
HRT012 Heart Valve Disease 57 0.086
127
BRN071 Brain Injury 54 0.086
128
MLR006 Male Reproductive Organ Cancer 50 0.086
129
P BDY007 Body Mass Index Quantitative Trait Locus 1 48 0.086
130
PRS042 Prostate Disease 47 0.086
131
VSC008 Vascular Hemostatic Disease 45 0.086
132
P PRS136 Prostate Cancer, Hereditary, 6 40 0.086
133
P PRS130 Prostate Cancer, Hereditary, 8 37 0.086
134
CRD220 Cardiac Valvular Defect, Developmental 36 0.086
135
KWS002 Kawasaki Disease 72 0.082
136
P ART101 Aortic Valve Disease 2 68 0.082
137
c MSC007 Muscle Hypertrophy 64 0.082
138
LYM019 Lymphosarcoma 59 0.082
139
RLP002 Relapsing-Remitting Multiple Sclerosis 59 0.082
140
LPD009 Lipid Storage Disease 53 0.082
141
HDN002 Head Injury 52 0.082
142
P HYP740 Hyperlipoproteinemia, Type V 51 0.082
143
c HYP073 Hypersensitivity Reaction Type Iv Disease 51 0.082
144
c VSC018 Visceral Steatosis 38 0.082
145
c CLR023 Colorectal Cancer 99 0.077
146
P LKM061 Leukemia, Acute Myeloid 83 0.077
147
c DLT002 Dilated Cardiomyopathy 74 0.077
148
c MYL006 Myeloid Leukemia 68 0.077
149
P CHR417 Chronic Graft Versus Host Disease 67 0.077
150
AGN016 Aging 63 0.077
151
HYP266 Hypoxia 63 0.077
152
c EXN002 Exanthem 62 0.077
153
c LYM031 Lymphocytic Leukemia 61 0.077
154
END030 End Stage Renal Failure 60 0.077
155
BRN106 Burns 59 0.077
156
BRN038 Bronchial Disease 58 0.077
157
CRN019 Coronary Artery Vasospasm 50 0.077
158
ACT118 Acute Non Lymphoblastic Leukemia 33 0.077
159
c LKM062 Leukemia, Acute Lymphoblastic 70 0.073
160
P ART138 Aortic Aneurysm, Familial Abdominal, 1 66 0.073
161
c THR014 Thrombocytopenia 65 0.073
162
P ACT074 Acute Lymphocytic Leukemia 62 0.073
163
PRP030 Purpura 62 0.073
164
c TRC086 Trichohepatoenteric Syndrome 1 61 0.073
165
NRM005 Neuromuscular Disease 61 0.073
166
P ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 60 0.073
167
URT039 Urticaria 60 0.073
168
CHL068 Cholestasis 60 0.073
169
IMP005 Impotence 58 0.073
170
LYM040 Lymphoblastic Lymphoma 58 0.073
171
BRN022 Bronchiectasis 58 0.073
172
LYM067 Lymphoid Leukemia 47 0.073
173
BRN080 Brain Ischemia 43 0.073
174
P HYP555 Hypertriglyceridemia, Transient Infantile 43 0.073
175
c PRC017 Precursor Lymphoblastic Lymphoma/leukemia 30 0.073
176
c PLM037 Pulmonary Hypertension 77 0.068
177
c HYP086 Hypothyroidism 66 0.068
178
c END044 Endometriosis 65 0.068
179
c VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 65 0.068
180
c PLY011 Polycystic Ovary Syndrome 64 0.068
181
GT001 Gout 62 0.068
182
GLC003 Glucose Intolerance 59 0.068
183
c NPH012 Nephrotic Syndrome 59 0.068
184
BNF002 Bone Fracture 50 0.068
185
EPD070 Epidermoid Cysts 50 0.068
186
PGM003 Pigmentation Disease 48 0.068
187
DST006 Diastolic Heart Failure 46 0.068
188
CLP006 Clopidogrel Resistance 45 0.068
189
OST012 Osteoarthritis 81 0.063
190
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.063
191
P HPT073 Hepatitis C Virus 73 0.063
192
P HPT001 Hepatitis C 69 0.063
193
LVR012 Liver Cirrhosis 67 0.063
194
c VSC011 Vasculitis 67 0.063
195
c HML002 Hemolytic Anemia 65 0.063
196
P LRG017 Large Intestine Cancer 63 0.063
197
PRM236 Primary Biliary Cholangitis 63 0.063
198
c HYP724 Hyperlipoproteinemia, Type Iii 61 0.063
199
c MYC008 Myocarditis 59 0.063
200
c DRR001 Diarrhea 58 0.063
201
BLD053 Blood Platelet Disease 56 0.063
202
CRD223 Cardiac Arrhythmia 56 0.063
203
MCL006 Macular Retinal Edema 55 0.063
204
c PRM006 Primary Biliary Cirrhosis 54 0.063
205
HMG005 Hemoglobinopathy 54 0.063
206
P CNG027 Congenital Hemolytic Anemia 52 0.063
207
HMZ003 Homozygous Familial Hypercholesterolemia 49 0.063
208
c CRN074 Coronary Artery Aneurysm 48 0.063
209
CPL005 Capillary Disease 47 0.063
210
P BLR024 Biliary Cirrhosis, Primary, 1 39 0.063
211
MYL069 Myeloma, Multiple 85 0.058
212
CRH001 Crohn's Disease 79 0.058
213
SCK003 Sickle Cell Anemia 75 0.058
214
P PLM164 Pulmonary Hypertension, Primary, 1 71 0.058
215
MYL009 Myelodysplastic Syndrome 71 0.058
216
c SLP006 Sleep Apnea 70 0.058
217
c PLM036 Pulmonary Fibrosis 70 0.058
218
APN008 Apnea, Obstructive Sleep 68 0.058
219
c CNJ013 Conjunctivitis 65 0.058
220
P VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 65 0.058
221
INT002 Intermittent Claudication 64 0.058
222
PPT005 Peptic Ulcer Disease 64 0.058
223
c NRP001 Neuropathy 63 0.058
224
c PNC044 Pancreatitis 62 0.058
225
c MYS005 Myositis 62 0.058
226
c GLM007 Glomerulonephritis 62 0.058
227
RTN018 Retinal Disease 58 0.058
228
c RCT021 Rectum Cancer 58 0.058
229
ART017 Aortic Disease 56 0.058
230
ACT058 Active Peptic Ulcer Disease 53 0.058
231
PRD004 Prediabetes Syndrome 51 0.058
232
ACT011 Acute Contagious Conjunctivitis 51 0.058
233
THY030 Thyroid Gland Disease 51 0.058
234
c ART084 Arteriovenous Fistula 50 0.058
235
URT010 Ureteral Obstruction 49 0.058
236
DBT008 Diabetic Angiopathy 48 0.058
237
P HYP739 Hyperlipoproteinemia, Type Iv 47 0.058
238
DLT018 Dilution, Pigmentary 31 0.058
239
HYP213 Hypomelanotic Disorder 26 0.058
240
VSC009 Vascular Skin Disease 20 0.058
241
MLR004 Malaria 85 0.052
242
c OVR042 Ovarian Cancer 83 0.052
243
P LKM071 Leukemia, Chronic Lymphocytic 78 0.052
244
GLB002 Glioblastoma 75 0.052
245
WRN001 Werner Syndrome 74 0.052
246
DPR016 Depression 73 0.052
247
c MCR115 Microvascular Complications of Diabetes 5 71 0.052
248
DSS008 Disease of Mental Health 70 0.052
249
c TBR001 Tuberous Sclerosis 69 0.052
250
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 67 0.052
251
c DRM010 Dermatomyositis 66 0.052
252
c SKN015 Skin Carcinoma 65 0.052
253
INT066 Interstitial Lung Disease 65 0.052
254
MNT002 Mental Depression 65 0.052
255
GLB015 Glioblastoma Multiforme 64 0.052
256
HYP056 Hypoglycemia 64 0.052
257
c CRD132 Cardiac Conduction Defect 64 0.052
258
c OVR049 Ovarian Disease 63 0.052
259
HDC001 Headache 63 0.052
260
BCT022 Bacterial Infectious Disease 63 0.052
261
SYN007 Synovitis 61 0.052
262
MCS002 Mucositis 60 0.052
263
c INF032 Infertility 60 0.052
264
c PLY041 Polymyositis 59 0.052
265
DBT062 Diabetic Foot Ulcers 59 0.052
266
c HYP061 Hypertrophic Cardiomyopathy 59 0.052
267
c PLY019 Polyneuropathy 58 0.052
268
P MCR113 Microvascular Complications of Diabetes 3 58 0.052
269
c ANG015 Angioedema 58 0.052
270
SCK005 Sickle Cell Disease 57 0.052
271
ACT103 Acute Lymphoblastic Leukemia, Childhood 55 0.052
272
c DBT005 Diabetes Insipidus 55 0.052
273
BNR002 Bone Resorption Disease 54 0.052
274
c OBS001 Obstructive Jaundice 54 0.052
275
c OVR046 Ovarian Cyst 52 0.052
276
CRN030 Coronary Stenosis 52 0.052
277
c RNL015 Renal Hypertension 49 0.052
278
GND003 Gonadal Disease 49 0.052
279
c SCL057 Scoliosis, Isolated 1 46 0.052
280
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 46 0.052
281
P MCR120 Microvascular Complications of Diabetes 7 46 0.052
282
ADS004 Aids Dementia Complex 45 0.052
283
CRB008 Cerebral Atherosclerosis 44 0.052
284
P MCR130 Microvascular Complications of Diabetes 6 43 0.052
285
P MCR133 Microvascular Complications of Diabetes 4 43 0.052
286
P PLY105 Polycystic Ovary Syndrome 1 43 0.052
287
c CRB088 Cerebral Atrophy 42 0.052
288
FXF002 Fox-Fordyce Disease 41 0.052
289
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 40 0.052
290
P BNM022 Bone Mineral Density Quantitative Trait Locus 8 40 0.052
291
P LKM004 Leukemia, B-Cell, Chronic 38 0.052
292
PCD001 Pica Disease 35 0.052
293
c PRX010 Paroxysmal Ventricular Fibrillation 32 0.052
294
CRC034 Carcinoma Showing Thymus-Like Differentiation 29 0.052
295
CYT017 Cytophagic Histiocytic Panniculitis 26 0.052
296
P HYP163 Hyperlipidemia Type 3 22 0.052
297
INT074 Intracranial Arteriosclerosis 16 0.052
298
c HPT023 Hepatocellular Carcinoma 97 0.045
299
c SRC025 Sarcoidosis 1 76 0.045
300
MNT001 Mantle Cell Lymphoma 75 0.045
301
P LKM063 Leukemia, Chronic Myeloid 74 0.045
302
LYM133 Lymphoma, Hodgkin, Classic 73 0.045
303
c DRM053 Dermatitis, Atopic 73 0.045
304
c EPL164 Epilepsy 73 0.045
305
P TBR025 Tuberous Sclerosis 1 72 0.045
306
P HPT016 Hepatitis B 70 0.045
307
c SYS005 Systemic Scleroderma 70 0.045
308
ALL003 Allergic Rhinitis 69 0.045
309
c AMY004 Amyloidosis 69 0.045
310
END057 Endometrial Cancer 69 0.045
311
DRM006 Dermatitis 69 0.045
312
P SCL052 Scleroderma, Familial Progressive 68 0.045
313
c WLD002 Waldenstrom Macroglobulinemia 68 0.045
314
OST003 Osteonecrosis 67 0.045
315
HSH003 Hashimoto Thyroiditis 67 0.045
316
ART005 Arteriovenous Malformation 66 0.045
317
c BCL006 B-Cell Lymphomas 66 0.045
318
c NSP012 Nasopharyngeal Carcinoma 66 0.045
319
P ATM011 Autoimmune Hepatitis 66 0.045
320
GST045 Gastroenteritis 65 0.045
321
P LCL006 Localized Scleroderma 65 0.045
322
c CRB048 Cerebral Cavernous Malformations 65 0.045
323
c GLL020 Gallbladder Disease 64 0.045
324
CNT047 Contact Dermatitis 64 0.045
325
PLM033 Pulmonary Embolism 64 0.045
326
c GLM040 Glioma Susceptibility 1 64 0.045
327
MYL031 Myeloproliferative Neoplasm 64 0.045
328
HMT002 Hematologic Cancer 64 0.045
329
MLN008 Melanoma 64 0.045
330
RNL114 Renal Cell Carcinoma, Nonpapillary 63 0.045
331
c RHN004 Rhinitis 63 0.045
332
GST049 Gastrointestinal System Cancer 62 0.045
333
c INT068 Intestinal Disease 62 0.045
334
SPP011 Suppression of Tumorigenicity 12 62 0.045
335
c CMR001 Camurati-Engelmann Disease 62 0.045
336
P PRC016 Pre-Eclampsia 61 0.045
337
RSC001 Rosacea 61 0.045
338
c HMN010 Hemangioma 61 0.045
339
c BPL003 Bipolar Disorder 61 0.045
340
c GRV001 Graves' Disease 61 0.045
341
ALL006 Allergic Asthma 61 0.045
342
CRH005 Crohn's Colitis 61 0.045
343
c SBS003 Substance Abuse 61 0.045
344
c UTR058 Uterine Anomalies 60 0.045
345
P VRL010 Viral Hepatitis 60 0.045
346
P INS002 in Situ Carcinoma 60 0.045
347
DBT010 Diabetic Neuropathy 60 0.045
348
PLM010 Pulmonary Edema 60 0.045
349
NTR005 Nutritional Deficiency Disease 60 0.045
350
PLM012 Pulmonary Sarcoidosis 59 0.045
351
PLC008 Placenta Disease 59 0.045
352
PRC013 Pericarditis 59 0.045
353
P MYT020 Myotonic Dystrophy 2 59 0.045
354
c KDN017 Kidney Cancer 59 0.045
355
P ACT027 Acute Pancreatitis 59 0.045
356
PTT009 Pituitary Gland Disease 59 0.045
357
ILT001 Ileitis 59 0.045
358
c ECL001 Eclampsia 59 0.045
359
CHL067 Cholecystitis 59 0.045
360
GLM004 Gliomatosis Cerebri 58 0.045
361
ICH054 Ichthyosis, X-Linked 58 0.045
362
IGG001 Iga Glomerulonephritis 58 0.045
363
NRT004 Neuritis 58 0.045
364
c CTR002 Cataract 58 0.045
365
DCT002 Ductal Carcinoma in Situ 58 0.045
366
DFF005 Diffuse Large B-Cell Lymphoma 58 0.045
367
VSC002 Vascular Dementia 58 0.045
368
EWN002 Ewing's Family of Tumors 57 0.045
369
P INF071 Inflammatory Bowel Disease 1 57 0.045
370
BRS099 Breast Ductal Carcinoma 57 0.045
371
P BRS049 Breast Carcinoma in Situ 56 0.045
372
TRM010 Traumatic Brain Injury 56 0.045
373
c GLM045 Glioma 56 0.045
374
c HYP076 Hyperthyroidism 56 0.045
375
c INF037 Inflammatory Bowel Disease 56 0.045
376
c PHR004 Pharynx Cancer 55 0.045
377
GTR002 Goiter 54 0.045
378
SCH012 Schizoaffective Disorder 54 0.045
379
MYL004 Myelodysplastic Myeloproliferative Cancer 54 0.045
380
c RTN022 Retinal Vein Occlusion 54 0.045
381
DFF035 Diffuse Cutaneous Systemic Sclerosis 54 0.045
382
MCR004 Macroglobulinemia 54 0.045
383
SXL003 Sexual Disorder 53 0.045
384
OVR063 Overnutrition 53 0.045
385
P ACT134 Acute Liver Failure 53 0.045
386
BLR006 Biliary Tract Disease 53 0.045
387
c CHL066 Cholangitis 52 0.045
388
BRT005 Barth Syndrome 52 0.045
389
DNT012 Dental Caries 52 0.045
390
IDP024 Idiopathic Inflammatory Myopathy 52 0.045
391
CVR006 Cavernous Hemangioma 52 0.045
392
EXP004 Exophthalmos 52 0.045
393
c RNV001 Renovascular Hypertension 52 0.045
394
RYN005 Raynaud Phenomenon 52 0.045
395
CHL004 Cholelithiasis 52 0.045
396
c BLD036 Bile Duct Disease 51 0.045
397
MCL027 Macular Dystrophy, Dominant Cystoid 51 0.045
398
c AST007 Astrocytoma 51 0.045
399
P CNT016 Central Retinal Vein Occlusion 50 0.045
400
PST011 Pustulosis of Palm and Sole 50 0.045
401
HYP043 Hyperandrogenism 50 0.045
402
LBL001 Lobular Neoplasia 50 0.045
403
c ART018 Aortic Valve Insufficiency 50 0.045
404
P CHR579 Chiari Malformation Type Ii 49 0.045
405
PRL017 Prolymphocytic Leukemia 49 0.045
406
ANR004 Anuria 49 0.045
407
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 49 0.045
408
ACT017 Acute Chest Syndrome 49 0.045
409
HYP025 Hyperphosphatemia 49 0.045
410
HRT015 Heritable Pulmonary Arterial Hypertension 48 0.045
411
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 48 0.045
412
CRN017 Coronary Thrombosis 47 0.045
413
HMF008 Hemifacial Atrophy, Progressive 47 0.045
414
P LTN004 Late-Onset Retinal Degeneration 47 0.045
415
CRB085 Cerebral Hemorrhage 46 0.045
416
MYC005 Myocardial Stunning 46 0.045
417
DBT002 Diabetic Autonomic Neuropathy 46 0.045
418
DFF003 Diffuse Scleroderma 46 0.045
419
c SDR002 Siderosis 46 0.045
420
NPH010 Nephrosclerosis 46 0.045
421
GST071 Gastrointestinal Carcinoma 46 0.045
422
CRB004 Cerebral Artery Occlusion 46 0.045
423
SYS003 Systolic Heart Failure 46 0.045
424
NSP003 Nasopharyngeal Disease 46 0.045
425
P ADL052 Adult Acute Lymphocytic Leukemia 46 0.045
426
CRV045 Cervical Intraepithelial Neoplasia 45 0.045
427
GNG003 Gingival Recession 45 0.045
428
RTR011 Retroperitoneal Fibrosis 44 0.045
429
PHT003 Phototoxic Dermatitis 44 0.045
430
HYP030 Hypoactive Sexual Desire Disorder 44 0.045
431
P HYP734 Hypercholesterolemia, Autosomal Dominant, Type B 44 0.045
432
BLD054 Blood Protein Disease 43 0.045
433
STR103 Streptococcus Pneumonia 43 0.045
434
BLL007 Bullous Skin Disease 42 0.045
435
P PRC031 Preeclampsia/eclampsia 1 41 0.045
436
DRG024 Drug Allergy 41 0.045
437
c CRC039 Coarctation of Aorta 40 0.045
438
P CNG031 Congenital Nervous System Abnormality 40 0.045
439
P MJR004 Major Affective Disorder 4 40 0.045
440
CVR010 Cavernous Malformation 40 0.045
441
SBV001 Subvalvular Aortic Stenosis 40 0.045
442
CRD170 Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 1 39 0.045
443
P ATM022 Autoimmune Myocarditis 39 0.045
444
ACL001 Acalculous Cholecystitis 39 0.045
445
ORB013 Orbital Disease 38 0.045
446
FCL003 Facial Hemiatrophy 38 0.045
447
FBR089 Fibrosclerosis, Multifocal 37 0.045
448
HYP114 Hypertensive Nephropathy 37 0.045
449
CHL013 Cholecystolithiasis 37 0.045
451
END034 Endocrine Exophthalmos 32 0.045
452
CRN006 Coronary Aneurysm 32 0.045
453
P MYC058 Myocardial Infarction 2 31 0.045
454
HDG004 Hodgkin's Granuloma 30 0.045
455
P CRT085 Carotid Intimal Medial Thickness 2 25 0.045
456
HPD002 Hepadnavirus Infection 25 0.045
457
P CRB051 Cerebral Cavernous Malformation, Familial 25 0.045
458
ULC005 Ulcer of Lower Limbs 24 0.045
459
HDG006 Hodgkin's Paragranuloma 22 0.045
460
P BLR016 Biliary Cirrhosis, Primary, 2 17 0.045
461
HRP008 Herpes Simiae 16 0.045
462
HYD004 Hydrops of Gallbladder 15 0.045
463
c LNG032 Lung Cancer 99 0.037
464
INS024 Insulin-Like Growth Factor I 83 0.037
465
PLM129 Pulmonary Disease, Chronic Obstructive 75 0.037
466
c MYS003 Myasthenia Gravis 74 0.037
467
ANX010 Anxiety 73 0.037
468
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 73 0.037
469
SRC014 Sarcoma 70 0.037
470
SVR097 Severe Cutaneous Adverse Reaction 69 0.037
471
OBS002 Obsessive-Compulsive Disorder 69 0.037
472
SKN019 Skin Melanoma 67 0.037
473
MVM001 Movement Disease 67 0.037
474
TXC005 Toxic Shock Syndrome 66 0.037
475
P ACT210 Acute Respiratory Distress Syndrome 66 0.037
476
P OVR114 Ovarian Cancer 1 66 0.037
477
SPN186 Spinal Cord Injury 66 0.037
478
PST028 Post-Traumatic Stress Disorder 63 0.037
479
c VNW001 Von Willebrand's Disease 63 0.037
480
HMR039 Hemorrhage, Intracerebral 62 0.037
481
MRB003 Morbid Obesity 62 0.037
482
c SZR006 Seizure Disorder 61 0.037
483
P PCH015 Pachyonychia Congenita 1 60 0.037
484
c FCL005 Focal Segmental Glomerulosclerosis 60 0.037
485
c HMR012 Hemorrhagic Fever 60 0.037
486
SFT003 Soft Tissue Sarcoma 60 0.037
487
c HYP069 Hyperparathyroidism 59 0.037
488
HYP190 Hypoalphalipoproteinemia, Primary 59 0.037
489
c MTR012 Mitral Valve Disease 58 0.037
490
CNS004 Constipation 58 0.037
491
CLN015 Colon Adenocarcinoma 57 0.037
492
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.037
493
LNG031 Lung Benign Neoplasm 56 0.037
494
P SCN007 Secondary Hyperparathyroidism 56 0.037
495
P MLG074 Malignant Mesenchymoma 55 0.037
496
HYP080 Hypogonadism 53 0.037
497
HMC014 Homocysteinemia 52 0.037
498
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 52 0.037
499
PRT030 Parathyroid Gland Disease 51 0.037
500
PST095 Post-Thrombotic Syndrome 51 0.037
501
FSH001 Fish-Eye Disease 51 0.037
502
ART031 Aortic Coarctation 50 0.037
503
c FML035 Familial Hyperlipidemia 50 0.037
504
DBT006 Diabetic Macular Edema 49 0.037
505
EBL001 Ebola Hemorrhagic Fever 49 0.037
506
HYP081 Hypolipoproteinemia 49 0.037
507
ANG011 Angiodysplasia 48 0.037
508
c ANL018 Analbuminemia 48 0.037
509
PMP004 Pemphigus Foliaceus 47 0.037
510
GYN001 Gynecomastia 47 0.037
511
P PCH012 Pachyonychia Congenita 2 47 0.037
512
SPN369 Spinal Disease 47 0.037
513
MMM006 Mammographic Density 47 0.037
514
MRG013 Mirage Syndrome 45 0.037
515
ALL014 Allergic Encephalomyelitis 43 0.037
516
P PCH010 Pachyonychia Congenita 3 42 0.037
517
RNL097 Renal Artery Disease 42 0.037
518
LCH001 Leech Infestation 40 0.037
519
ACT084 Acute Stress Disorder 39 0.037
520
MDD003 Middle Cerebral Artery Infarction 37 0.037
521
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 37 0.037
522
P VRL017 Viral Hemorrhagic Fever 36 0.037
523
P HYP600 Hyperaldosteronism, Familial, Type Ii 36 0.037
524
P MYS011 Myasthenia Gravis Congenital 33 0.037
525
NTR027 Neutrophil Actin Dysfunction 32 0.037
526
EXF003 Exfoliative Dermatitis 30 0.037
527
RNL001 Renal Artery Obstruction 30 0.037
528
P HYP805 Hypercholesterolemia, Autosomal Dominant, 3 29 0.037
529
LYM053 Lymphomatous Thyroiditis 27 0.037
530
DRL001 Dural Sinus Malformation 23 0.037
531
BNG080 Benign Childhood Occipital Epilepsy, Gastaut Type 19 0.037
532
P CNG336 Congenital Analbuminemia 15 0.037
533
NNH003 Non-Hodgkin Lymphoma, Childhood 14 0.037
534
c PNC035 Pancreatic Cancer 83 0.026
535
c FNC027 Fanconi Anemia, Complementation Group a 81 0.026
536
ULC004 Ulcerative Colitis 80 0.026
537
BRN028 Brain Cancer 74 0.026
538
PSY004 Psychotic Disorder 74 0.026
539
c RTN024 Retinoblastoma 73 0.026
540
CHG001 Chagas Disease 73 0.026
541
c FML011 Familial Adenomatous Polyposis 72 0.026
542
BRC012 Brucellosis 71 0.026
543
ACR007 Acromegaly 71 0.026
544
c BLD134 Bladder Cancer 71 0.026
545
MYL005 Myelofibrosis 70 0.026
546
P MGR028 Migraine with or Without Aura 1 69 0.026
547
c PSD087 Pseudoxanthoma Elasticum 68 0.026
548
LYM007 Lymphangioleiomyomatosis 68 0.026
549
c HYP098 Hypereosinophilic Syndrome 67 0.026
550
c ART067 Aortic Aneurysm, Familial Thoracic 1 67 0.026
551
c MJR001 Major Depressive Disorder 67 0.026
552
GST092 Gastroesophageal Reflux 66 0.026
553
TTN003 Tetanus 66 0.026
554
c PRP019 Peripheral Nervous System Disease 66 0.026
555
DFC004 Deficiency Anemia 65 0.026
556
c CHR071 Charcot-Marie-Tooth Disease 65 0.026
557
CLT003 Colitis 65 0.026
558
CHL065 Cholangiocarcinoma 65 0.026
559
HYP020 Hyperprolactinemia 64 0.026
560
WLL001 Williams-Beuren Syndrome 64 0.026
561
HRP004 Herpes Zoster 63 0.026
562
GST033 Gestational Diabetes 63 0.026
563
CYT008 Cytomegalovirus Infection 61 0.026
564
c PRT013 Portal Hypertension 61 0.026
565
c NTR004 Neutropenia 61 0.026
566
c SJG008 Sjogren Syndrome 60 0.026
567
c SNS001 Sensorineural Hearing Loss 60 0.026
568
SQM006 Squamous Cell Carcinoma 59 0.026
569
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 59 0.026
570
PLG002 Plague 59 0.026
571
BRN004 Brain Edema 59 0.026
572
PLS007 Plasmodium Falciparum Malaria 58 0.026
573
c CYS018 Cystitis 58 0.026
574
c SPN052 Spondyloarthropathy 58 0.026
575
c TMP001 Temporal Lobe Epilepsy 57 0.026
576
c MNC007 Monocytic Leukemia 57 0.026
577
c PMP001 Pemphigus 56 0.026
578
P HYP731 Hyperaldosteronism, Familial, Type I 56 0.026
579
PRS021 Prostatic Adenoma 55 0.026
580
c INT070 Intestinal Obstruction 55 0.026
581
INT079 Intrahepatic Cholangiocarcinoma 55 0.026
582
SPN051 Spondylitis 55 0.026
583
PRP016 Paraplegia 55 0.026
584
P PSR017 Psoriasis 2 54 0.026
585
PNG002 Pain Agnosia 54 0.026
586
ATN002 Autonomic Nervous System Disease 54 0.026
587
c THY032 Thyroiditis 54 0.026
588
QDR001 Quadriplegia 53 0.026
589
SPR004 Supravalvular Aortic Stenosis 53 0.026
590
CRY003 Cryptosporidiosis 53 0.026
591
AMN003 Amnestic Disorder 53 0.026
592
ESN015 Eosinophilic Fasciitis 53 0.026
593
PRS129 Prostatic Hyperplasia, Benign 53 0.026
594
c CMP008 Compartment Syndrome 52 0.026
595
c MLN007 Male Infertility 52 0.026
596
c PTY003 Pityriasis Rubra Pilaris 52 0.026
597
SPN119 Spondylarthropathy 52 0.026
598
c MTC069 Mitochondrial Disorders 51 0.026
599
DBT004 Diabetic Polyneuropathy 50 0.026
600
FSC004 Fasciitis 50 0.026
601
HDR003 Hidradenitis 49 0.026
602
c DYS021 Dysautonomia 49 0.026
603
JHN001 Johanson-Blizzard Syndrome 48 0.026
604
RSS026 Roussy-Levy Hereditary Areflexic Dystasia 48 0.026
605
P INF145 Infantile Liver Failure Syndrome 1 48 0.026
606
ORL015 Oral Squamous Cell Carcinoma 48 0.026
607
HPT025 Hepatic Lipase Deficiency 47 0.026
608
MCR037 Macroglossia 47 0.026
609
TND004 Tendinopathy 47 0.026
610
ASP030 Aspirin Resistance 46 0.026
611
MDL020 Midline Interhemispheric Variant of Holoprosencephaly 46 0.026
612
ASP007 Aspiration Pneumonia 46 0.026
613
GLC086 Glucocorticoid-Induced Osteoporosis 46 0.026
614
TND005 Tendinitis 45 0.026
615
CRS001 Crescentic Glomerulonephritis 45 0.026
616
BLP005 Blepharitis 45 0.026
617
CNN001 Cannabis Dependence 44 0.026
618
INT010 Intracranial Embolism 44 0.026
619
SPS057 Spasticity 44 0.026
620
P PSR028 Psoriasis 7 43 0.026
621
P PSR032 Psoriasis 11 43 0.026
622
BLN006 Blind Loop Syndrome 43 0.026
623
P LKM056 Leukemia, Chronic Lymphocytic 2 43 0.026
624
P PSR018 Psoriasis 13 42 0.026
625
CNN002 Cannabis Abuse 42 0.026
626
HYP064 Hypogonadotropism 42 0.026
627
OVR094 Ovarian Epithelial Cancer 41 0.026
628
c IGN003 Iga Nephropathy 1 41 0.026
629
HMR023 Hemorrhagic Cystitis 41 0.026
630
MTR007 Motor Peripheral Neuropathy 41 0.026
631
FXD003 Fixed Drug Eruption 40 0.026
632
SCR035 Sacral Agenesis with Vertebral Anomalies 40 0.026
633
c CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 39 0.026
634
NRV004 Nerve Compression Syndrome 39 0.026
635
P RCR022 Recurrent Acute Pancreatitis 39 0.026
636
HRN029 Hearing Loss, Noise-Induced 37 0.026
637
P CHR096 Chronic Pulmonary Heart Disease 37 0.026
638
SCL056 Sclerosing Cholangitis, Neonatal 37 0.026
639
HYP264 Hypertonia 37 0.026
640
c ANT001 Anterolateral Myocardial Infarction 37 0.026
641
c HYP658 Hypoplastic Amelogenesis Imperfecta 33 0.026
642
PMP009 Pemphigus Erythematosus 30 0.026
643
CHT005 Chitotriosidase Deficiency 28 0.026
644
INF021 Infant Gynecomastia 27 0.026
645
SLR005 Solar Urticaria 27 0.026
646
XP2001 Xp22.3 Microdeletion Syndrome 26 0.026
647
DGS002 Degos 'en Cocarde' Erythrokeratoderma 26 0.026
648
SLN001 Silent Myocardial Infarction 24 0.026
649
NCR015 Necrotizing Autoimmune Myopathy 24 0.026
650
PRQ002 Paraquat Poisoning 22 0.026
651
DST089 Distal Trisomy 3p 22 0.026
652
INF009 Inflammatory Spondylopathy 21 0.026
653
MTC135 Mitochondrial Import-Stimulating Factor 18 0.026
Content
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