Search results for Simvastatin

659 hits were found for Simvastatin

# Family MCID Name MIFTS Score
1
LPD008 Lipid Metabolism Disorder 65 0.475
2
c CRN300 Coronary Heart Disease 1 62 0.308
3
c CRN018 Coronary Artery Anomaly 74 0.302
4
c DBT026 Diabetes Mellitus, Noninsulin-Dependent 92 0.286
5
ISC006 Ischemic Heart Disease 72 0.283
6
c HRT032 Heart Disease 76 0.281
7
c CRD246 Cardiovascular System Disease 57 0.266
8
ISC004 Ischemia 67 0.256
9
c DBT009 Diabetes Mellitus 67 0.255
10
ART140 Arteries, Anomalies of 67 0.255
11
c ART021 Arteriosclerosis 61 0.253
12
VSC007 Vascular Disease 72 0.244
13
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 53 0.234
14
c HYP607 Hypercholesterolemia, Familial 82 0.223
15
GLC008 Glucose Metabolism Disease 54 0.220
16
c MYC007 Myocardial Infarction 78 0.217
17
c KDN018 Kidney Disease 71 0.171
18
c LVR013 Liver Disease 77 0.167
19
CRB039 Cerebrovascular Disease 70 0.161
20
ATM095 Autoimmune Disease 68 0.159
21
GST050 Gastrointestinal System Disease 67 0.152
22
c MYP004 Myopathy 65 0.150
23
c PRD008 Periodontitis 66 0.146
24
c HYP614 Hyperlipidemia, Familial Combined 56 0.143
25
LNG099 Lung Disease 70 0.139
26
URN009 Urinary System Disease 59 0.139
27
c MLT020 Multiple Sclerosis 76 0.136
28
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.136
29
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 58 0.134
30
c MSC033 Muscle Disorders 56 0.134
31
c BRS047 Breast Cancer 100 0.131
32
LVR012 Liver Cirrhosis 67 0.131
33
c ENC018 Encephalopathy 65 0.131
34
GST049 Gastrointestinal System Cancer 62 0.131
35
HYP060 Hyperinsulinism 57 0.131
36
GST071 Gastrointestinal Carcinoma 46 0.131
37
P CHR089 Chronic Kidney Failure 73 0.129
38
c ALZ034 Alzheimer Disease 88 0.126
39
ANG054 Angina Pectoris 70 0.126
41
c CLR023 Colorectal Cancer 99 0.123
42
RSP006 Respiratory System Disease 64 0.123
43
c INT068 Intestinal Disease 62 0.123
44
P ACT210 Acute Respiratory Distress Syndrome 66 0.121
45
HYP066 Hyperglycemia 65 0.121
46
OCL033 Oculocerebral Syndrome with Hypopigmentation 46 0.121
47
c PLY011 Polycystic Ovary Syndrome 64 0.118
48
P PRD040 Periodontitis, Chronic 60 0.118
49
PRP027 Peripheral Vascular Disease 72 0.115
50
CNG034 Congestive Heart Failure 71 0.115
51
c PRT013 Portal Hypertension 61 0.115
52
c LNG032 Lung Cancer 99 0.112
53
c HPT021 Hepatitis 74 0.112
54
SKN016 Skin Disease 68 0.112
55
MTH009 Mouth Disease 66 0.112
56
DMN002 Dementia 69 0.109
57
P ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 67 0.109
58
c LYM033 Lymphoproliferative Syndrome 63 0.109
59
IMM136 Immune System Disease 57 0.109
60
INT253 Intestinal Benign Neoplasm 57 0.109
61
PRP080 Peripheral Artery Disease 56 0.109
62
c HYP073 Hypersensitivity Reaction Type Iv Disease 51 0.109
63
MYL069 Myeloma, Multiple 85 0.106
64
AST005 Asthma 81 0.106
65
c NRV007 Nervous System Disease 72 0.106
66
PRD007 Periodontal Disease 66 0.106
67
DMY004 Demyelinating Disease 60 0.106
68
SKN027 Skin Conditions 51 0.106
69
c ART022 Arthritis 78 0.103
70
PSY004 Psychotic Disorder 74 0.103
71
BRS051 Breast Disease 68 0.103
72
CNN005 Connective Tissue Disease 67 0.103
73
P LRG017 Large Intestine Cancer 63 0.103
74
c MYS005 Myositis 62 0.103
75
GLC003 Glucose Intolerance 59 0.103
76
RCT017 Rectal Disease 42 0.103
77
c RHM011 Rheumatoid Arthritis 82 0.100
78
END030 End Stage Renal Failure 60 0.100
79
c HMR003 Hemorrhagic Disease 59 0.100
80
P ACT075 Acute Myocardial Infarction 57 0.100
81
c BLD051 Blood Coagulation Disease 51 0.100
82
VSC008 Vascular Hemostatic Disease 45 0.100
83
c PRS040 Prostate Cancer 93 0.096
84
c PLM037 Pulmonary Hypertension 77 0.096
85
PLM129 Pulmonary Disease, Chronic Obstructive 75 0.096
86
P CNT035 Central Nervous System Disease 65 0.096
87
CLN019 Colonic Disease 62 0.096
88
MSC190 Muscular Disease 55 0.096
89
BLD054 Blood Protein Disease 43 0.096
90
MSC004 Muscle Tissue Disease 39 0.096
91
c DBT085 Diabetes Mellitus, Insulin-Dependent 73 0.093
92
c SCH015 Schizophrenia 73 0.093
93
P HPT003 Hepatitis a 66 0.093
94
STR067 Stroke, Ischemic 84 0.089
95
P HYP595 Hypertension, Essential 77 0.089
96
c LPS004 Lupus Erythematosus 69 0.089
97
SMT004 Smith-Lemli-Opitz Syndrome 69 0.089
98
FTT001 Fatty Liver Disease 66 0.089
99
c OVR049 Ovarian Disease 63 0.089
100
P ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 60 0.089
101
PNC034 Pancreas Disease 60 0.089
102
RLP002 Relapsing-Remitting Multiple Sclerosis 59 0.089
103
c OVR046 Ovarian Cyst 52 0.089
104
P PNC106 Pancreatic Agenesis 1 52 0.089
105
INT007 Intermediate Coronary Syndrome 50 0.089
106
P MTR002 Mitral Valve Insufficiency 50 0.089
107
GND003 Gonadal Disease 49 0.089
108
P OPT051 Opitz Gbbb Syndrome, Type I 48 0.089
109
P PLY105 Polycystic Ovary Syndrome 1 43 0.089
110
P SYS001 Systemic Lupus Erythematosus 88 0.085
111
c ADN016 Adenocarcinoma 71 0.085
112
VRC005 Varicose Veins 67 0.085
113
ACQ007 Acquired Immunodeficiency Syndrome 66 0.085
114
HMN014 Human Immunodeficiency Virus Infectious Disease 62 0.085
115
c INF032 Infertility 60 0.085
116
c ALP008 Alopecia 56 0.085
117
LNG031 Lung Benign Neoplasm 56 0.085
118
SPS003 Spastic Diplegia 49 0.085
119
BRN039 Bronchial Neoplasm 43 0.085
120
c PNC035 Pancreatic Cancer 83 0.081
121
c LKM002 Leukemia 72 0.081
122
c PNM007 Pneumonia 72 0.081
123
VRL011 Viral Infectious Disease 69 0.081
124
THR100 Thrombocytopenic Purpura, Autoimmune 68 0.081
125
AGN016 Aging 63 0.081
126
P THR001 Thrombocytopenia Due to Platelet Alloimmunization 61 0.081
127
IMP005 Impotence 58 0.081
128
NRT004 Neuritis 58 0.081
129
CRT016 Carotid Artery Disease 58 0.081
130
DPR016 Depression 73 0.077
131
ART016 Aortic Aneurysm 71 0.077
132
P SML038 Small Cell Cancer of the Lung 69 0.077
133
c ALP009 Alopecia Areata 68 0.077
134
P ART138 Aortic Aneurysm, Familial Abdominal, 1 66 0.077
135
c VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 65 0.077
136
RHM027 Rheumatic Disease 65 0.077
137
HPT019 Hepatic Encephalopathy 60 0.077
138
SCH012 Schizoaffective Disorder 54 0.077
139
P SCN036 Secondary Progressive Multiple Sclerosis 53 0.077
140
PRD004 Prediabetes Syndrome 51 0.077
141
HPT004 Hepatic Coma 45 0.077
142
c OST002 Osteoporosis 74 0.073
143
DSS008 Disease of Mental Health 70 0.073
144
c HYP086 Hypothyroidism 66 0.073
145
MNT002 Mental Depression 65 0.073
146
c NRP001 Neuropathy 63 0.073
147
P FTT008 Fatty Liver Disease, Nonalcoholic 1 61 0.073
148
CHL068 Cholestasis 60 0.073
149
c NNL004 Nonalcoholic Fatty Liver Disease 56 0.073
150
c OPT009 Optic Neuritis 55 0.073
151
ESP002 Esophageal Varix 51 0.073
152
P PRS136 Prostate Cancer, Hereditary, 6 40 0.073
153
P PRS130 Prostate Cancer, Hereditary, 8 37 0.073
154
c HPT023 Hepatocellular Carcinoma 97 0.068
155
GST053 Gastric Cancer 78 0.068
156
c PRK057 Parkinson Disease, Late-Onset 77 0.068
157
SCK003 Sickle Cell Anemia 75 0.068
158
c CLC063 Celiac Disease 1 72 0.068
159
c ATR011 Atrial Fibrillation 69 0.068
160
c ART023 Arthropathy 68 0.068
161
SPN186 Spinal Cord Injury 66 0.068
162
c HML002 Hemolytic Anemia 65 0.068
163
BND020 Bone Disease 65 0.068
164
JNT002 Joint Disorders 64 0.068
165
HMR039 Hemorrhage, Intracerebral 62 0.068
166
TRN015 Transient Cerebral Ischemia 59 0.068
167
P MCR113 Microvascular Complications of Diabetes 3 58 0.068
168
BRN038 Bronchial Disease 58 0.068
169
c RCT021 Rectum Cancer 58 0.068
170
SCK005 Sickle Cell Disease 57 0.068
171
STM006 Stomach Disease 56 0.068
172
LYM024 Lymphatic System Disease 55 0.068
173
c DBT005 Diabetes Insipidus 55 0.068
174
P ACT071 Acute Kidney Failure 54 0.068
175
HMG005 Hemoglobinopathy 54 0.068
176
c OBS001 Obstructive Jaundice 54 0.068
177
P CNG027 Congenital Hemolytic Anemia 52 0.068
178
c CLL015 Collagen Disease 52 0.068
179
CRB085 Cerebral Hemorrhage 46 0.068
180
P MCR120 Microvascular Complications of Diabetes 7 46 0.068
181
P MCR130 Microvascular Complications of Diabetes 6 43 0.068
182
P MCR133 Microvascular Complications of Diabetes 4 43 0.068
183
c CRB088 Cerebral Atrophy 42 0.068
184
CYS001 Cystic Fibrosis 83 0.063
185
c INF038 Influenza 75 0.063
186
c EPL164 Epilepsy 73 0.063
187
P PLM164 Pulmonary Hypertension, Primary, 1 71 0.063
188
c AMY004 Amyloidosis 69 0.063
189
P ART101 Aortic Valve Disease 2 68 0.063
190
MVM001 Movement Disease 67 0.063
191
c DRM010 Dermatomyositis 66 0.063
192
c END044 Endometriosis 65 0.063
193
MLN008 Melanoma 64 0.063
194
BCT022 Bacterial Infectious Disease 63 0.063
195
c PNC044 Pancreatitis 62 0.063
196
NRM005 Neuromuscular Disease 61 0.063
197
ALL006 Allergic Asthma 61 0.063
198
c NPH012 Nephrotic Syndrome 59 0.063
199
ESP023 Esophageal Disease 59 0.063
200
LMY002 Leiomyoma 58 0.063
201
c DRR001 Diarrhea 58 0.063
202
HRT012 Heart Valve Disease 57 0.063
203
MYM001 Myoma 57 0.063
204
TRM010 Traumatic Brain Injury 56 0.063
205
BRN071 Brain Injury 54 0.063
206
BNR002 Bone Resorption Disease 54 0.063
207
ACT058 Active Peptic Ulcer Disease 53 0.063
208
P ACT134 Acute Liver Failure 53 0.063
209
MLR006 Male Reproductive Organ Cancer 50 0.063
210
PRS042 Prostate Disease 47 0.063
211
MTC005 Mitochondrial Metabolism Disease 46 0.063
212
CNN004 Connective Tissue Cancer 46 0.063
213
SCH003 Schizophreniform Disorder 43 0.063
214
c VSC018 Visceral Steatosis 38 0.063
215
CRD220 Cardiac Valvular Defect, Developmental 36 0.063
216
MNS002 Mini Stroke 25 0.063
217
PHK010 Phakomatosis Spilorosea 18 0.063
218
P HPT073 Hepatitis C Virus 73 0.058
219
CRZ001 Crouzon Syndrome 70 0.058
220
P HPT001 Hepatitis C 69 0.058
221
DRM006 Dermatitis 69 0.058
222
P SCL052 Scleroderma, Familial Progressive 68 0.058
223
LYM007 Lymphangioleiomyomatosis 68 0.058
224
OST159 Osteogenic Sarcoma 67 0.058
225
c MJR001 Major Depressive Disorder 67 0.058
226
CLF027 Cleft Palate, Isolated 66 0.058
227
c PRP019 Peripheral Nervous System Disease 66 0.058
228
INT002 Intermittent Claudication 64 0.058
229
HYP056 Hypoglycemia 64 0.058
230
PRM236 Primary Biliary Cholangitis 63 0.058
231
c UVT001 Uveitis 62 0.058
232
c SZR006 Seizure Disorder 61 0.058
233
c SML001 Small Cell Carcinoma 61 0.058
234
P INS002 in Situ Carcinoma 60 0.058
235
END040 Endogenous Depression 59 0.058
236
c KDN017 Kidney Cancer 59 0.058
237
P ACT027 Acute Pancreatitis 59 0.058
238
c HYP040 Hypospadias 59 0.058
239
RTN018 Retinal Disease 58 0.058
240
DCT002 Ductal Carcinoma in Situ 58 0.058
241
END035 Endocrine Gland Cancer 57 0.058
242
BRS099 Breast Ductal Carcinoma 57 0.058
243
LMY014 Leiomyoma, Uterine 57 0.058
244
P BRS049 Breast Carcinoma in Situ 56 0.058
245
c PRM006 Primary Biliary Cirrhosis 54 0.058
246
LPD009 Lipid Storage Disease 53 0.058
247
IDP024 Idiopathic Inflammatory Myopathy 52 0.058
248
P HYP740 Hyperlipoproteinemia, Type V 51 0.058
249
TRP008 Tropical Calcific Pancreatitis 50 0.058
250
HYP043 Hyperandrogenism 50 0.058
251
c ARC016 Auriculocondylar Syndrome 1 48 0.058
252
HYP748 Hypertelorism 48 0.058
253
P BDY007 Body Mass Index Quantitative Trait Locus 1 48 0.058
254
PGM003 Pigmentation Disease 48 0.058
255
DYS018 Dysostosis 48 0.058
256
UVL010 Uveal Disease 45 0.058
257
P OPT050 Opitz Gbbb Syndrome, Type Ii 44 0.058
258
BRN080 Brain Ischemia 43 0.058
259
GNT050 Genitourinary Tract Anomalies 41 0.058
260
ACR002 Acrocapitofemoral Dysplasia 40 0.058
261
P BLR024 Biliary Cirrhosis, Primary, 1 39 0.058
262
PNL013 Penile Disease 39 0.058
263
STR018 Steroid Inherited Metabolic Disorder 35 0.058
264
P TRC078 Trichohepatoenteric Syndrome 2 35 0.058
265
DLT018 Dilution, Pigmentary 31 0.058
266
HYP213 Hypomelanotic Disorder 26 0.058
267
INS024 Insulin-Like Growth Factor I 83 0.051
268
P LKM071 Leukemia, Chronic Lymphocytic 78 0.051
269
c RTN024 Retinoblastoma 73 0.051
270
P TBR025 Tuberous Sclerosis 1 72 0.051
271
c BLD134 Bladder Cancer 71 0.051
272
c MCR115 Microvascular Complications of Diabetes 5 71 0.051
273
P HPT016 Hepatitis B 70 0.051
274
c TBR001 Tuberous Sclerosis 69 0.051
275
PRT036 Peritonitis 67 0.051
276
c MSC005 Muscular Dystrophy 66 0.051
277
TXC005 Toxic Shock Syndrome 66 0.051
278
CHL123 Chlamydia 66 0.051
279
c CRD119 Cardiac Arrest 66 0.051
280
MDD011 Mood Disorder 65 0.051
281
c THR014 Thrombocytopenia 65 0.051
282
c CRB048 Cerebral Cavernous Malformations 65 0.051
283
c MSC007 Muscle Hypertrophy 64 0.051
284
THR024 Thrombosis 64 0.051
285
c PLY014 Polycystic Kidney Disease 63 0.051
286
c TRC086 Trichohepatoenteric Syndrome 1 61 0.051
287
c LYM031 Lymphocytic Leukemia 61 0.051
288
c BPL003 Bipolar Disorder 61 0.051
289
MCS002 Mucositis 60 0.051
290
P PCH015 Pachyonychia Congenita 1 60 0.051
291
SLP005 Sleep Disorder 60 0.051
292
DBT010 Diabetic Neuropathy 60 0.051
293
P MYT020 Myotonic Dystrophy 2 59 0.051
294
c PLM034 Pulmonary Emphysema 59 0.051
295
c CTR002 Cataract 58 0.051
296
c RHB003 Rhabdomyosarcoma 57 0.051
297
ERY017 Erythema Elevatum Diutinum 55 0.051
298
c LCT001 Lactic Acidosis 53 0.051
299
c CMP008 Compartment Syndrome 52 0.051
300
P HRM017 Hermansky-Pudlak Syndrome 2 52 0.051
301
BSL008 Basal Ganglia Disease 49 0.051
302
P PNC128 Pain - Chronic 46 0.051
303
CHL147 Chlamydia Pneumonia 42 0.051
304
STR015 Stereotypic Movement Disorder 42 0.051
305
P CNG031 Congenital Nervous System Abnormality 40 0.051
306
P MJR004 Major Affective Disorder 4 40 0.051
307
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 40 0.051
308
MYF001 Myofibroma 38 0.051
309
P LKM004 Leukemia, B-Cell, Chronic 38 0.051
311
INT053 Intracranial Vasospasm 31 0.051
312
CRC034 Carcinoma Showing Thymus-Like Differentiation 29 0.051
313
RPD005 Rapidly Involuting Congenital Hemangioma 24 0.051
314
DRL001 Dural Sinus Malformation 23 0.051
315
BNG080 Benign Childhood Occipital Epilepsy, Gastaut Type 19 0.051
316
c RTN008 Retinitis Pigmentosa 79 0.045
317
NRF026 Neurofibromatosis, Type Iv, of Riccardi 76 0.045
318
c DLT002 Dilated Cardiomyopathy 74 0.045
319
WRN001 Werner Syndrome 74 0.045
320
BRN028 Brain Cancer 74 0.045
321
EWN003 Ewing Sarcoma 74 0.045
322
LYM133 Lymphoma, Hodgkin, Classic 73 0.045
323
c NRB001 Neuroblastoma 73 0.045
324
c RSP003 Respiratory Failure 72 0.045
325
ADR007 Adrenoleukodystrophy 72 0.045
326
c HRP006 Herpes Simplex 71 0.045
327
SRC014 Sarcoma 70 0.045
328
P THR092 Thrombophilia Due to Thrombin Defect 70 0.045
329
ALC007 Alcohol Dependence 70 0.045
330
BRN024 Bronchitis 70 0.045
331
c LYM118 Lymphoma 69 0.045
332
P MGR028 Migraine with or Without Aura 1 69 0.045
333
P NRF024 Neurofibromatosis, Type I 69 0.045
334
c WLD002 Waldenstrom Macroglobulinemia 68 0.045
335
ALL026 Allergic Hypersensitivity Disease 68 0.045
336
P WLM013 Wilms Tumor 1 68 0.045
337
GST045 Gastroenteritis 65 0.045
338
CRB011 Cerebrotendinous Xanthomatosis 65 0.045
339
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.045
340
ADN018 Adenoma 65 0.045
341
c SNS014 Sinusitis 64 0.045
342
CNT047 Contact Dermatitis 64 0.045
343
P WLM018 Wilms Tumor 5 64 0.045
344
PLM033 Pulmonary Embolism 64 0.045
345
c CRD132 Cardiac Conduction Defect 64 0.045
346
RNL114 Renal Cell Carcinoma, Nonpapillary 63 0.045
347
RHM001 Rheumatic Fever 63 0.045
348
HDC001 Headache 63 0.045
349
TRN018 Transitional Cell Carcinoma 63 0.045
350
HYP266 Hypoxia 63 0.045
351
ERY003 Erythema Multiforme 63 0.045
352
ECT006 Ectodermal Dysplasia 62 0.045
353
ATY005 Atypical Teratoid Rhabdoid Tumor 62 0.045
354
PRP030 Purpura 62 0.045
355
c BNC003 Bone Cancer 61 0.045
356
OCL009 Ocular Cancer 61 0.045
357
c GRV001 Graves' Disease 61 0.045
358
c NTR004 Neutropenia 61 0.045
359
c NRV006 Nervous System Cancer 60 0.045
360
OPT006 Optic Nerve Disease 60 0.045
361
SFT003 Soft Tissue Sarcoma 60 0.045
362
c INT030 Intracranial Aneurysm 60 0.045
363
P MCL013 Mucolipidosis Iv 59 0.045
364
LYM019 Lymphosarcoma 59 0.045
365
GLM004 Gliomatosis Cerebri 58 0.045
366
c PLY019 Polyneuropathy 58 0.045
367
c HYP750 Hypertriglyceridemia, Familial 58 0.045
368
RHB001 Rhabdoid Cancer 58 0.045
369
BLD044 Bladder Disease 57 0.045
370
c RHB008 Rhabdoid Tumor Predisposition Syndrome 1 57 0.045
371
EWN002 Ewing's Family of Tumors 57 0.045
372
HYP005 Hypokalemia 56 0.045
373
HPT022 Hepatoblastoma 56 0.045
374
MSC072 Muscle Cancer 56 0.045
375
c GLM045 Glioma 56 0.045
376
c HYP076 Hyperthyroidism 56 0.045
377
NTR046 Neutrophil Migration 56 0.045
378
DXT001 Dextrocardia 55 0.045
379
NNL002 Nonalcoholic Steatohepatitis 55 0.045
380
KRT009 Keratosis 55 0.045
381
SPN041 Spinal Cord Disease 55 0.045
382
CHR081 Choroideremia 55 0.045
383
P MLG074 Malignant Mesenchymoma 55 0.045
384
GTR002 Goiter 54 0.045
385
XNT003 Xanthomatosis 54 0.045
386
c NLD001 Nail Disease 54 0.045
387
LMB062 Limb Ischemia 54 0.045
388
MCR004 Macroglobulinemia 54 0.045
389
SXL003 Sexual Disorder 53 0.045
390
PRM020 Premenstrual Tension 53 0.045
391
CLC006 Calcinosis 53 0.045
392
RHM028 Rheumatic Heart Disease 52 0.045
393
CRT013 Carotid Stenosis 52 0.045
394
c EST001 Estrogen-Receptor Positive Breast Cancer 52 0.045
395
RTN015 Retinal Cancer 52 0.045
396
HDN002 Head Injury 52 0.045
397
NSD001 Nose Disease 52 0.045
398
GRN017 Granulocytopenia 52 0.045
399
CNG184 Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects 52 0.045
400
EXP004 Exophthalmos 52 0.045
401
RNL077 Renal Fibrosis 51 0.045
402
PRN021 Paranasal Sinus Disease 51 0.045
403
FSH001 Fish-Eye Disease 51 0.045
404
MTB004 Metabolic Acidosis 51 0.045
405
THY030 Thyroid Gland Disease 51 0.045
406
P CLR017 Clear Cell Sarcoma 50 0.045
407
DBT004 Diabetic Polyneuropathy 50 0.045
408
P BPL002 Bipolar I Disorder 50 0.045
409
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 49 0.045
410
HYP017 Hypophosphatemia 48 0.045
411
HRT015 Heritable Pulmonary Arterial Hypertension 48 0.045
412
P HNT004 Huntington Disease-Like 2 48 0.045
413
CMP028 Complement Component 2 Deficiency 47 0.045
414
HMF008 Hemifacial Atrophy, Progressive 47 0.045
415
LYM067 Lymphoid Leukemia 47 0.045
416
DBT002 Diabetic Autonomic Neuropathy 46 0.045
417
NPH010 Nephrosclerosis 46 0.045
418
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 46 0.045
420
HYP030 Hypoactive Sexual Desire Disorder 44 0.045
421
P PLM022 Pulmonary Valve Insufficiency 44 0.045
422
P HYP555 Hypertriglyceridemia, Transient Infantile 43 0.045
423
CRN031 Cranial Nerve Disease 43 0.045
424
PRV003 Perivascular Epithelioid Cell Tumor 42 0.045
425
P PCH010 Pachyonychia Congenita 3 42 0.045
426
ORN001 Ornithosis 42 0.045
427
RCT020 Rectum Adenocarcinoma 41 0.045
428
P HNT011 Huntington Disease-Like 3 40 0.045
429
P BNM022 Bone Mineral Density Quantitative Trait Locus 8 40 0.045
430
BNS001 Bone Osteosarcoma 40 0.045
431
P VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 39 0.045
432
GST020 Gastric Antral Vascular Ectasia 39 0.045
433
PSD088 Pseudobulbar Affect 39 0.045
434
ORB013 Orbital Disease 38 0.045
435
FCL003 Facial Hemiatrophy 38 0.045
436
CHR079 Choroid Disease 37 0.045
437
HYP114 Hypertensive Nephropathy 37 0.045
438
GRM010 Germ Cells Tumors 36 0.045
439
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 35 0.045
440
SBC016 Subacute Delirium 34 0.045
441
FST001 Foster-Kennedy Syndrome 33 0.045
442
GNR003 Generalized Atherosclerosis 33 0.045
443
END034 Endocrine Exophthalmos 32 0.045
444
P MYC058 Myocardial Infarction 2 31 0.045
445
HDG004 Hodgkin's Granuloma 30 0.045
446
ACT094 Acute Articular Rheumatism 29 0.045
447
P RHB011 Rhabdoid Tumor Predisposition Syndrome 2 27 0.045
448
HPD002 Hepadnavirus Infection 25 0.045
449
HRN028 Horns in Sheep 24 0.045
450
HDG006 Hodgkin's Paragranuloma 22 0.045
451
HRP008 Herpes Simiae 16 0.045
452
c OVR042 Ovarian Cancer 83 0.036
453
c LNG064 Lung Cancer Susceptibility 3 80 0.036
454
c NNN008 Noonan Syndrome 1 79 0.036
455
P LKM063 Leukemia, Chronic Myeloid 74 0.036
456
LPD012 Lipoid Congenital Adrenal Hyperplasia 72 0.036
457
BRC012 Brucellosis 71 0.036
458
c PLM036 Pulmonary Fibrosis 70 0.036
459
c ATS364 Autism 68 0.036
460
OST003 Osteonecrosis 67 0.036
461
SKN019 Skin Melanoma 67 0.036
462
ADN011 Adenoid Cystic Carcinoma 67 0.036
463
P MCR129 Microvascular Complications of Diabetes 1 66 0.036
464
INT146 Intervertebral Disc Disease 65 0.036
465
c THR005 Thrombotic Thrombocytopenic Purpura 65 0.036
466
c ADL010 Adult Respiratory Distress Syndrome 64 0.036
467
c BLD062 Bile Duct Cancer 64 0.036
468
SPN404 Spinal and Bulbar Muscular Atrophy, X-Linked 1 62 0.036
469
GT001 Gout 62 0.036
470
c EXN002 Exanthem 62 0.036
471
c GLM007 Glomerulonephritis 62 0.036
472
c HMN010 Hemangioma 61 0.036
473
ATH013 Atherosclerosis Susceptibility 61 0.036
474
P ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.036
475
NWB001 Newborn Respiratory Distress Syndrome 61 0.036
476
P VRL010 Viral Hepatitis 60 0.036
477
SQM006 Squamous Cell Carcinoma 59 0.036
478
ILT001 Ileitis 59 0.036
479
P FML116 Familial Cold Autoinflammatory Syndrome 1 58 0.036
480
MCL006 Macular Retinal Edema 55 0.036
481
c SLL003 Salla Disease 53 0.036
482
ALP097 Alopecia Universalis Congenita 53 0.036
483
c GNT009 Giant Axonal Neuropathy 52 0.036
484
CRN030 Coronary Stenosis 52 0.036
485
CVR006 Cavernous Hemangioma 52 0.036
486
MCL027 Macular Dystrophy, Dominant Cystoid 51 0.036
487
PRT018 Portal Vein Thrombosis 51 0.036
488
c HRD018 Hair Disease 50 0.036
489
EPD070 Epidermoid Cysts 50 0.036
490
c HYP087 Hypotrichosis 50 0.036
491
P CHR579 Chiari Malformation Type Ii 49 0.036
492
HMZ003 Homozygous Familial Hypercholesterolemia 49 0.036
493
URT010 Ureteral Obstruction 49 0.036
494
DBT008 Diabetic Angiopathy 48 0.036
495
P PCH012 Pachyonychia Congenita 2 47 0.036
496
ASP030 Aspirin Resistance 46 0.036
497
ATN004 Autonomic Neuropathy 46 0.036
498
RTR008 Root Resorption 45 0.036
499
P GLL024 Gallbladder Disease 1 45 0.036
500
TND005 Tendinitis 45 0.036
501
P GNT049 Giant Axonal Neuropathy 1, Autosomal Recessive 43 0.036
502
c OCY003 Oocyte Maturation Defect 1 42 0.036
503
P MCR112 Microvascular Complications of Diabetes 2 42 0.036
504
CVR010 Cavernous Malformation 40 0.036
505
CRN020 Coronary Restenosis 39 0.036
506
RSP007 Respiratory Distress Syndrome, Infant 38 0.036
507
BCK003 Background Diabetic Retinopathy 38 0.036
508
P HYP600 Hyperaldosteronism, Familial, Type Ii 36 0.036
509
CHR463 Chronic Actinic Dermatitis 34 0.036
510
P CRB051 Cerebral Cavernous Malformation, Familial 25 0.036
511
P PSD047 Pseudo-Turner Syndrome 25 0.036
512
SLN001 Silent Myocardial Infarction 24 0.036
513
DST081 Distal Trisomy 11q 20 0.036
514
NNC012 Non-Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency 16 0.036
515
PLM119 Pulmonary Artery Coming from Patent Ductus Arteriosus 14 0.036
516
MLR004 Malaria 85 0.026
518
ESP021 Esophageal Cancer 84 0.026
519
OST012 Osteoarthritis 81 0.026
520
ULC004 Ulcerative Colitis 80 0.026
521
c WSK001 Wiskott-Aldrich Syndrome 76 0.026
522
PLY001 Polycythemia Vera 76 0.026
523
c NRF023 Neurofibromatosis, Type Ii 76 0.026
524
ANX010 Anxiety 73 0.026
525
CHG001 Chagas Disease 73 0.026
526
THY028 Thyroid Cancer 72 0.026
527
LSH001 Leishmaniasis 72 0.026
528
c MNN013 Meningitis 71 0.026
529
c MTC003 Metachromatic Leukodystrophy 71 0.026
530
END057 Endometrial Cancer 69 0.026
531
P ATR087 Atrial Standstill 1 69 0.026
532
CTN007 Cutaneous Leishmaniasis 68 0.026
533
c MYL006 Myeloid Leukemia 68 0.026
534
c PRP003 Porphyria Cutanea Tarda 67 0.026
535
PNC033 Pancreas Adenocarcinoma 67 0.026
536
c HYP098 Hypereosinophilic Syndrome 67 0.026
537
HSH003 Hashimoto Thyroiditis 67 0.026
538
c ART067 Aortic Aneurysm, Familial Thoracic 1 67 0.026
539
c PSR002 Psoriasis 67 0.026
540
MSC157 Muscular Dystrophy, Duchenne Type 66 0.026
541
P DPH024 Diaphragmatic Hernia, Congenital 66 0.026
542
c HYD006 Hydrocephalus 66 0.026
543
P LPM012 Lipomatosis, Multiple 66 0.026
544
HLC007 Helicobacter Pylori Infection 66 0.026
545
c SPN046 Spinal Muscular Atrophy 65 0.026
546
ANP031 Anaplastic Thyroid Cancer 65 0.026
547
CLT003 Colitis 65 0.026
548
CHL065 Cholangiocarcinoma 65 0.026
549
WLL001 Williams-Beuren Syndrome 64 0.026
550
CMP010 Complex Regional Pain Syndrome 64 0.026
551
INC002 Inclusion Body Myositis 64 0.026
552
P MST023 Mesothelioma, Malignant 63 0.026
553
GST033 Gestational Diabetes 63 0.026
554
SPN027 Spinal Stenosis 62 0.026
555
P PRC016 Pre-Eclampsia 61 0.026
556
c FBR017 Fibrosarcoma 61 0.026
557
STT001 Status Epilepticus 61 0.026
558
P BCT007 Bacterial Meningitis 61 0.026
559
ACT119 Acute Promyelocytic Leukemia 61 0.026
560
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 61 0.026
561
c HYP724 Hyperlipoproteinemia, Type Iii 61 0.026
562
c SBS003 Substance Abuse 61 0.026
563
c GST044 Gastritis 61 0.026
564
LYS012 Lysosomal Acid Lipase Deficiency 60 0.026
565
c PRP029 Porphyria 60 0.026
566
c PLY018 Polycythemia 60 0.026
567
c PLY041 Polymyositis 59 0.026
568
c MMB011 Membranous Nephropathy 59 0.026
569
BRN106 Burns 59 0.026
570
c HYP061 Hypertrophic Cardiomyopathy 59 0.026
571
BRN004 Brain Edema 59 0.026
572
c LCH002 Lichen Planus 59 0.026
573
c CYS018 Cystitis 58 0.026
574
GST023 Gastric Ulcer 58 0.026
575
VSC002 Vascular Dementia 58 0.026
576
c TMP001 Temporal Lobe Epilepsy 57 0.026
577
c LKD001 Leukodystrophy 57 0.026
578
P INF023 Inflammatory Breast Carcinoma 57 0.026
579
P CNG216 Congenital Hydrocephalus 56 0.026
580
P HYP731 Hyperaldosteronism, Familial, Type I 56 0.026
581
c MSC003 Muscular Atrophy 56 0.026
582
c AGG001 Aggressive Periodontitis 56 0.026
583
PRS021 Prostatic Adenoma 55 0.026
584
INT079 Intrahepatic Cholangiocarcinoma 55 0.026
585
THR004 Thrombocytosis 55 0.026
586
c CTN003 Cutaneous Lupus Erythematosus 55 0.026
587
P PYR010 Peyronie's Disease 55 0.026
588
PNC041 Pancreatic Ductal Adenocarcinoma 54 0.026
589
PNG002 Pain Agnosia 54 0.026
590
TTH006 Tooth Disease 54 0.026
591
c THY032 Thyroiditis 54 0.026
592
RTN020 Retinal Vascular Disease 54 0.026
593
c DPY001 Dupuytren Contracture 53 0.026
594
CHR100 Chronic Ulcer of Skin 53 0.026
595
PRN023 Prion Disease 53 0.026
596
SPR004 Supravalvular Aortic Stenosis 53 0.026
597
RTN003 Retinal Ischemia 53 0.026
598
ESN015 Eosinophilic Fasciitis 53 0.026
599
HMC014 Homocysteinemia 52 0.026
600
c PTY003 Pityriasis Rubra Pilaris 52 0.026
601
c MTC133 Mitochondrial Myopathy 52 0.026
602
DGN001 Degenerative Disc Disease 51 0.026
603
KLD001 Keloids 51 0.026
604
CRN019 Coronary Artery Vasospasm 50 0.026
605
BNF002 Bone Fracture 50 0.026
606
PST011 Pustulosis of Palm and Sole 50 0.026
607
c FML035 Familial Hyperlipidemia 50 0.026
608
FSC004 Fasciitis 50 0.026
609
c ART084 Arteriovenous Fistula 50 0.026
610
HYP088 Hyper-Igd Syndrome 49 0.026
611
c ATR005 Atrophic Gastritis 49 0.026
612
NDL021 Nodular Lymphocyte Predominant Hodgkin Lymphoma 49 0.026
613
PRX014 Proximal Spinal Muscular Atrophy 49 0.026
614
PRP017 Periapical Periodontitis 48 0.026
615
JHN001 Johanson-Blizzard Syndrome 48 0.026
616
P INF145 Infantile Liver Failure Syndrome 1 48 0.026
617
GSG001 Gas Gangrene 48 0.026
618
MCR011 Microinvasive Gastric Cancer 47 0.026
619
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 47 0.026
620
CHL056 Cheilitis 47 0.026
621
TND004 Tendinopathy 47 0.026
622
MYC005 Myocardial Stunning 46 0.026
623
GLC086 Glucocorticoid-Induced Osteoporosis 46 0.026
624
P SBC035 Subacute Cutaneous Lupus Erythematosus 45 0.026
625
c RPP006 Rippling Muscle Disease 2 45 0.026
626
CRB086 Cerebral Aneurysms 44 0.026
627
ALL014 Allergic Encephalomyelitis 43 0.026
628
MNN017 Mononeuropathy 43 0.026
629
FLL031 Follicular Adenoma 43 0.026
630
P LKM056 Leukemia, Chronic Lymphocytic 2 43 0.026
631
ACT167 Acute Generalized Exanthematous Pustulosis 43 0.026
632
c BNG032 Benign Mesothelioma 42 0.026
633
SCR011 Scrapie 42 0.026
634
HMR023 Hemorrhagic Cystitis 41 0.026
635
PRT019 Protein-Losing Enteropathy 41 0.026
636
RFR010 Refractory Anemia 41 0.026
637
LWT001 Low Tension Glaucoma 40 0.026
638
DNT014 Dental Pulp Disease 40 0.026
639
PLM005 Pleomorphic Lipoma 39 0.026
640
P ATM100 Autoimmune Optic Neuritis 39 0.026
641
CYT002 Cytokine Deficiency 39 0.026
642
c TRC005 Tracheal Stenosis 39 0.026
643
CND006 Candida Glabrata 38 0.026
644
INT323 Intraocular Pressure Quantitative Trait Locus 38 0.026
645
XNT009 Xanthoma Disseminatum 37 0.026
646
LCH013 Lichen Planus Pemphigoides 36 0.026
647
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 36 0.026
648
DNT006 Dental Pulp Necrosis 34 0.026
649
CHL070 Cholesterol Embolism 33 0.026
650
NTR027 Neutrophil Actin Dysfunction 32 0.026
651
SML011 Smoldering Myeloma 32 0.026
652
DFC001 Defective Apolipoprotein B-100 32 0.026
653
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 29 0.026
654
P ANR046 Aniridia 3 29 0.026
655
P HYP805 Hypercholesterolemia, Autosomal Dominant, 3 29 0.026
656
c MRL001 Meralgia Paresthetica 27 0.026
657
CYT017 Cytophagic Histiocytic Panniculitis 26 0.026
658
HML018 Homologous Wasting Disease 25 0.026
659
SLF012 Sulfite Oxidase Deficiency Due to Molybdenum Cofactor Deficiency 23 0.026
Content
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