Search results for Atorvastatin

1013 hits were found for Atorvastatin

# Family MCID Name MIFTS Score
1
c HYP836 Hypercholesterolemia, Familial, 1 73 41.479
2
LPD008 Lipid Metabolism Disorder 62 33.141
3
P CRN300 Coronary Heart Disease 1 73 26.652
4
LPP008 Lipoprotein Quantitative Trait Locus 65 22.274
5
ATH013 Atherosclerosis Susceptibility 63 21.230
6
ART140 Arteries, Anomalies of 53 20.513
7
ISC004 Ischemia 61 19.600
8
P HRT032 Heart Disease 81 19.371
9
c TYP009 Type 2 Diabetes Mellitus 92 18.618
10
P MYP004 Myopathy 67 16.446
11
P MYC007 Myocardial Infarction 70 15.651
12
P DBT009 Diabetes Mellitus 67 15.500
13
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 15.022
14
c FML021 Familial Hypercholesterolemia 72 14.663
15
INT007 Intermediate Coronary Syndrome 54 13.660
16
P HYP750 Hypertriglyceridemia, Familial 62 13.092
17
P VSC007 Vascular Disease 63 12.977
18
FML035 Familial Hyperlipidemia 55 12.280
19
c ACT075 Acute Myocardial Infarction 56 11.779
20
ANG054 Angina Pectoris 66 11.231
21
P ATR011 Atrial Fibrillation 66 10.736
22
STR067 Stroke, Ischemic 80 10.732
23
c CHR684 Chronic Kidney Disease 69 10.567
24
c HYP272 Hypercholesterolemia, Familial, 3 45 10.220
25
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 10.214
26
P KDN018 Kidney Disease 72 10.092
27
NNL005 Non-Alcoholic Fatty Liver Disease 63 10.086
28
FTT001 Fatty Liver Disease 62 10.062
29
PRT251 Proteinuria, Chronic Benign 57 9.907
30
CRB039 Cerebrovascular Disease 66 9.603
31
P CRD246 Cardiovascular System Disease 56 9.440
32
PRP027 Peripheral Vascular Disease 71 9.177
33
48X005 48,xyyy 39 9.018
34
CNG034 Congestive Heart Failure 69 8.957
35
TRN015 Transient Cerebral Ischemia 63 8.484
36
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 8.476
37
c HYP595 Hypertension, Essential 85 8.239
38
NNL006 Non-Alcoholic Steatohepatitis 54 8.236
39
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 8.209
40
c ATR087 Atrial Standstill 1 74 7.809
41
c HYP724 Hyperlipoproteinemia, Type Iii 67 7.612
42
P MLT020 Multiple Sclerosis 79 7.604
43
CRB004 Cerebral Artery Occlusion 45 7.590
44
P PRD008 Periodontitis 64 7.590
45
HMZ003 Homozygous Familial Hypercholesterolemia 60 7.426
46
P LPS004 Lupus Erythematosus 61 7.406
47
P PRS040 Prostate Cancer 95 7.247
48
c ACT071 Acute Kidney Failure 60 7.196
49
P HYP838 Hyperlipidemia, Familial Combined, 3 61 7.194
50
P RHM011 Rheumatoid Arthritis 82 7.121
51
CRT013 Carotid Stenosis 51 7.112
52
P PLM037 Pulmonary Hypertension 72 7.110
53
HYP066 Hyperglycemia 61 7.094
54
BRN071 Brain Injury 50 6.863
55
IMP005 Impotence 52 6.844
56
P PLY011 Polycystic Ovary Syndrome 57 6.772
57
P ART021 Arteriosclerosis 54 6.748
58
c SYS001 Systemic Lupus Erythematosus 87 6.691
59
P LVR013 Liver Disease 69 6.514
60
c MCR130 Microvascular Complications of Diabetes 6 41 6.457
61
c MCR120 Microvascular Complications of Diabetes 7 47 6.457
62
c MCR113 Microvascular Complications of Diabetes 3 52 6.457
63
c MCR133 Microvascular Complications of Diabetes 4 41 6.457
64
ANR040 Aneurysm 61 6.433
65
RPD005 Rapidly Involuting Congenital Hemangioma 46 6.291
66
P ART022 Arthritis 71 6.261
67
RLP002 Relapsing-Remitting Multiple Sclerosis 56 6.239
68
P ALZ034 Alzheimer Disease 87 6.212
69
AGN016 Aging 54 6.162
70
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 6.156
71
CYT002 Cytokine Deficiency 43 6.139
72
TRM010 Traumatic Brain Injury 51 6.090
73
P MYS005 Myositis 56 5.996
74
END086 End Stage Renal Disease 52 5.995
75
P CRD119 Cardiac Arrest 67 5.976
76
HYP266 Hypoxia 57 5.891
77
c TYP008 Type 1 Diabetes Mellitus 70 5.855
78
c PRD040 Periodontitis, Chronic 52 5.718
79
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 5.572
80
ANT039 Antisynthetase Syndrome 55 5.457
81
GLB002 Glioblastoma 67 5.351
82
P BRS047 Breast Cancer 98 5.347
83
LVR012 Liver Cirrhosis 63 5.330
84
HMC014 Homocysteinemia 52 5.228
85
PRP080 Peripheral Artery Disease 54 5.134
86
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 5.133
87
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 5.133
88
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 5.133
89
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 5.133
90
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 5.133
91
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 5.133
92
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 5.133
93
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 5.133
94
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 5.133
95
c DLT002 Dilated Cardiomyopathy 78 5.121
96
HYP081 Hypolipoproteinemia 49 5.106
97
THR024 Thrombosis 56 5.014
98
c BLD140 Blood Group, I System 46 5.011
99
BNR002 Bone Resorption Disease 47 4.971
100
ART016 Aortic Aneurysm 68 4.923
101
P OST002 Osteoporosis 76 4.854
102
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 4.854
103
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 4.854
104
P END044 Endometriosis 62 4.816
105
c THR092 Thrombophilia Due to Thrombin Defect 74 4.808
106
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 63 4.766
107
OST012 Osteoarthritis 77 4.722
108
P NPH012 Nephrotic Syndrome 60 4.720
109
GSG001 Gas Gangrene 52 4.706
110
c HPT001 Hepatitis C 62 4.681
111
ALL014 Allergic Encephalomyelitis 34 4.667
112
P PSR002 Psoriasis 63 4.639
113
PST011 Pustulosis of Palm and Sole 52 4.639
114
KWS002 Kawasaki Disease 65 4.635
115
P GRF003 Graft-Versus-Host Disease 71 4.616
116
P THR014 Thrombocytopenia 66 4.597
117
HMN044 Human Immunodeficiency Virus Type 1 78 4.536
118
PLM129 Pulmonary Disease, Chronic Obstructive 74 4.535
119
c HPT003 Hepatitis a 63 4.528
120
P AST005 Asthma 76 4.522
121
CRN030 Coronary Stenosis 50 4.499
122
c PLM164 Pulmonary Hypertension, Primary, 1 76 4.487
123
c HPT073 Hepatitis C Virus 71 4.471
124
ATM095 Autoimmune Disease 61 4.464
125
CHL068 Cholestasis 61 4.464
126
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 4.445
127
c MCR115 Microvascular Complications of Diabetes 5 65 4.365
128
GLC003 Glucose Intolerance 54 4.357
129
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 4.345
130
c ACT135 Acute Graft Versus Host Disease 51 4.342
131
P MYC008 Myocarditis 59 4.311
132
CRT016 Carotid Artery Disease 52 4.310
133
P SLP006 Sleep Apnea 69 4.309
134
OCL069 Ocular Motor Apraxia 57 4.254
135
P HPT023 Hepatocellular Carcinoma 96 4.162
136
P SZR006 Seizure Disorder 70 4.130
137
CRD132 Cardiac Conduction Defect 60 4.109
138
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 4.084
139
ADN018 Adenoma 59 4.079
140
SPN186 Spinal Cord Injury 61 4.033
141
SVR004 Severe Combined Immunodeficiency 72 4.025
142
END072 Endotheliitis 36 4.017
143
P PLM036 Pulmonary Fibrosis 66 3.955
144
IMM167 Immune Deficiency Disease 78 3.943
145
c HYP740 Hyperlipoproteinemia, Type V 53 3.917
146
P ANR048 Aniridia 1 64 3.912
147
GLL048 Glial Tumor 52 3.905
148
GLM045 Glioma 63 3.905
149
P CRN074 Coronary Artery Aneurysm 42 3.903
150
47X002 47,xyy 48 3.891
151
P EXN002 Exanthem 58 3.874
152
APN008 Apnea, Obstructive Sleep 67 3.847
153
P PNM007 Pneumonia 67 3.794
154
c SCL052 Scleroderma, Familial Progressive 61 3.789
155
P PNC044 Pancreatitis 61 3.774
156
PRM236 Primary Biliary Cholangitis 60 3.747
157
c ART101 Aortic Valve Disease 2 66 3.744
158
c ACT027 Acute Pancreatitis 60 3.741
159
CRH001 Crohn's Disease 80 3.707
160
c ART115 Aortic Valve Disease 1 74 3.672
161
P BRN022 Bronchiectasis 60 3.670
162
P HYP086 Hypothyroidism 69 3.668
163
c PCH010 Pachyonychia Congenita 3 43 3.651
164
BRN004 Brain Edema 54 3.651
165
P EPL164 Epilepsy 68 3.624
166
URT010 Ureteral Obstruction 45 3.618
167
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 3.606
168
RHB024 Rhabdomyosarcoma 2 67 3.592
169
P HYP061 Hypertrophic Cardiomyopathy 69 3.553
170
P HPT021 Hepatitis 69 3.543
171
DPR016 Depression 65 3.536
172
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 3.442
173
CLT003 Colitis 63 3.421
174
P TBR001 Tuberous Sclerosis 69 3.381
175
CLR108 Colorectal Adenoma 64 3.361
176
P ADN016 Adenocarcinoma 63 3.357
177
PRT013 Portal Hypertension 59 3.308
178
CNS004 Constipation 56 3.273
179
P THY032 Thyroiditis 57 3.273
180
P BCL017 B-Cell Lymphoma 59 3.271
181
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 3.254
182
P DBT005 Diabetes Insipidus 54 3.244
183
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 3.244
184
HRT012 Heart Valve Disease 53 3.242
185
P LNG032 Lung Cancer 98 3.230
186
PRP030 Purpura 54 3.219
187
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 3.214
188
P GLM007 Glomerulonephritis 60 3.161
189
URL001 Urolithiasis 46 3.150
190
LTN004 Late-Onset Retinal Degeneration 60 3.116
191
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 3.089
192
RYN005 Raynaud Phenomenon 45 3.083
193
HMN014 Human Immunodeficiency Virus Infectious Disease 54 3.080
194
ADL002 Adult Syndrome 70 3.065
195
ALC007 Alcohol Dependence 66 3.064
196
RCK004 Rickets 68 3.041
197
P PNC035 Pancreatic Cancer 86 3.008
198
c ATM011 Autoimmune Hepatitis 63 2.992
199
DST006 Diastolic Heart Failure 45 2.989
200
c MJR022 Major Affective Disorder 8 38 2.984
201
c MJR024 Major Affective Disorder 9 41 2.984
202
P BPL003 Bipolar Disorder 56 2.984
203
RNL114 Renal Cell Carcinoma, Nonpapillary 80 2.969
204
INT030 Intracranial Aneurysm 55 2.969
205
MNT002 Mental Depression 57 2.968
206
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 2.949
207
P MCR129 Microvascular Complications of Diabetes 1 68 2.941
208
c MCR112 Microvascular Complications of Diabetes 2 42 2.941
209
GT001 Gout 64 2.925
210
PRT036 Peritonitis 65 2.898
211
HYP056 Hypoglycemia 65 2.885
212
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 2.884
213
c TBR025 Tuberous Sclerosis 1 84 2.884
214
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 2.883
215
CLP006 Clopidogrel Resistance 44 2.881
216
P LKM062 Leukemia, Acute Lymphoblastic 69 2.879
217
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 2.877
218
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 2.877
219
P VSC011 Vasculitis 61 2.859
220
P TRN020 Turner Syndrome 67 2.853
221
P LYM118 Lymphoma 67 2.846
222
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 2.845
223
c FML001 Familial Atrial Fibrillation 65 2.836
224
LPT014 Leptin Deficiency or Dysfunction 78 2.833
225
P INS002 in Situ Carcinoma 53 2.823
226
P CRC039 Coarctation of Aorta 46 2.823
227
P PLY041 Polymyositis 59 2.801
228
MLR004 Malaria 80 2.796
230
INT002 Intermittent Claudication 61 2.785
231
P SYS005 Systemic Scleroderma 74 2.779
232
PLM033 Pulmonary Embolism 58 2.761
233
DFC004 Deficiency Anemia 74 2.757
234
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 2.756
235
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 2.756
236
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 2.735
237
HYP555 Hypertriglyceridemia, Transient Infantile 38 2.728
238
STT001 Status Epilepticus 59 2.718
239
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 2.716
240
CRT084 Creatinine Clearance Quantitative Trait Locus 25 2.705
241
P LKM071 Leukemia, Chronic Lymphocytic 75 2.704
242
LYM007 Lymphangioleiomyomatosis 68 2.674
243
P BRS044 Breast Adenocarcinoma 58 2.674
244
HYP014 Hyperuricemia 51 2.674
245
P GST044 Gastritis 55 2.658
246
P BLD134 Bladder Cancer 79 2.657
247
P DRM010 Dermatomyositis 61 2.633
248
P NRP001 Neuropathy 60 2.629
249
P LKM002 Leukemia 67 2.628
250
c ATM022 Autoimmune Myocarditis 36 2.628
251
c SML038 Small Cell Cancer of the Lung 69 2.628
252
ENT004 Enthesopathy 51 2.595
253
P HMN010 Hemangioma 62 2.553
254
NSP002 Nasopharyngitis 45 2.531
255
P DMN002 Dementia 66 2.531
256
c HYP839 Hyperlipidemia, Familial Combined, 1 30 2.514
257
LPD009 Lipid Storage Disease 45 2.501
258
CLN015 Colon Adenocarcinoma 65 2.497
259
c PRS136 Prostate Cancer, Hereditary, 6 33 2.490
260
c PRS130 Prostate Cancer, Hereditary, 8 32 2.490
261
PRS047 Prostatitis 58 2.490
262
c HNT004 Huntington Disease-Like 2 52 2.485
263
P NRB001 Neuroblastoma 66 2.485
264
AMN003 Amnestic Disorder 54 2.485
265
SVR001 Severe Acute Respiratory Syndrome 67 2.451
266
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 2.435
267
P TMP001 Temporal Lobe Epilepsy 49 2.435
268
MDD011 Mood Disorder 62 2.429
269
P HYP098 Hypereosinophilic Syndrome 66 2.420
270
ACQ007 Acquired Immunodeficiency Syndrome 59 2.398
271
MYL069 Myeloma, Multiple 77 2.394
272
HYP060 Hyperinsulinism 54 2.388
273
c CHR711 Chronic Asthma 41 2.384
274
P FCL005 Focal Segmental Glomerulosclerosis 57 2.384
275
c VRL010 Viral Hepatitis 53 2.382
277
P FNG006 Feingold Syndrome 1 62 2.374
278
c HPT016 Hepatitis B 62 2.369
279
HYP025 Hyperphosphatemia 48 2.348
280
c SPN225 Spondyloarthropathy 1 70 2.341
281
CLB022 Coloboma, Ocular, Autosomal Recessive 28 2.339
282
RNL077 Renal Fibrosis 46 2.339
283
P SNS001 Sensorineural Hearing Loss 59 2.338
284
c HNT011 Huntington Disease-Like 3 34 2.329
285
CHL065 Cholangiocarcinoma 58 2.329
286
P NTR004 Neutropenia 63 2.329
287
INT079 Intrahepatic Cholangiocarcinoma 51 2.329
288
P ALC033 Alcohol Use Disorder 61 2.311
289
IGG001 Iga Glomerulonephritis 50 2.293
290
SYN036 Syncope 45 2.289
291
SQM006 Squamous Cell Carcinoma 60 2.289
292
PRP016 Paraplegia 52 2.285
293
P MJR001 Major Depressive Disorder 68 2.273
294
CRB009 Cerebritis 43 2.272
295
MCS002 Mucositis 56 2.259
296
SBC016 Subacute Delirium 43 2.250
297
c LKM061 Leukemia, Acute Myeloid 83 2.218
298
PRC013 Pericarditis 53 2.183
299
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 2.165
300
TXC005 Toxic Shock Syndrome 62 2.159
301
BCT022 Bacterial Infectious Disease 56 2.154
302
MCL006 Macular Retinal Edema 57 2.154
303
DMY004 Demyelinating Disease 50 2.150
304
P CLR023 Colorectal Cancer 100 2.146
305
HDN002 Head Injury 44 2.128
306
ART004 Aortic Atherosclerosis 47 2.127
307
P MTR012 Mitral Valve Disease 57 2.127
308
P DRR001 Diarrhea 55 2.127
309
GST092 Gastroesophageal Reflux 61 2.104
310
CVD001 Covid-19 57 2.093
311
P MYS003 Myasthenia Gravis 68 2.091
312
ALL029 Allergic Disease 59 2.091
313
TND004 Tendinopathy 45 2.069
314
TND005 Tendinitis 54 2.069
315
c BRN108 Branchiootic Syndrome 1 62 2.069
316
INF118 Inflammatory Myopathy with Abundant Macrophages 27 2.069
317
DRM006 Dermatitis 62 2.069
318
KDN013 Kidney Hypertrophy 34 2.069
319
HML018 Homologous Wasting Disease 21 2.043
320
ASP030 Aspirin Resistance 40 2.037
321
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 2.014
322
c SCN036 Secondary Progressive Multiple Sclerosis 55 2.009
323
HYP043 Hyperandrogenism 48 2.009
324
P URT039 Urticaria 58 2.002
325
SPN051 Spondylitis 51 1.993
326
INF009 Inflammatory Spondylopathy 30 1.993
327
NTR005 Nutritional Deficiency Disease 61 1.976
328
P AVS003 Avascular Necrosis 41 1.974
329
PRQ002 Paraquat Poisoning 28 1.954
330
NRT004 Neuritis 53 1.954
331
AND005 Androgen Insensitivity Syndrome, Mild 21 1.950
332
c MGR028 Migraine with or Without Aura 1 64 1.945
333
HYP540 Hypertension, Diastolic 37 1.945
334
ULC004 Ulcerative Colitis 74 1.945
335
P MLN008 Melanoma 76 1.945
336
NCR015 Necrotizing Autoimmune Myopathy 27 1.937
337
DWN001 Down Syndrome 70 1.925
338
P MYL006 Myeloid Leukemia 61 1.918
339
P CRB048 Cerebral Cavernous Malformations 63 1.910
340
CVR010 Cavernous Malformation 30 1.910
341
P TRM003 Tremor 48 1.879
342
P CND004 Candidiasis 58 1.879
343
GYN001 Gynecomastia 47 1.879
344
INF021 Infant Gynecomastia 30 1.879
345
P PLY019 Polyneuropathy 52 1.879
346
P RTN024 Retinoblastoma 73 1.879
347
HYP080 Hypogonadism 50 1.879
348
P INF038 Influenza 68 1.864
349
MYC005 Myocardial Stunning 46 1.856
350
P PRP019 Peripheral Nervous System Disease 58 1.834
351
c PRC016 Pre-Eclampsia 65 1.833
352
c AMY091 Amyotrophic Lateral Sclerosis 1 88 1.819
353
ORL015 Oral Squamous Cell Carcinoma 43 1.819
354
P LTR001 Lateral Sclerosis 58 1.819
355
FNG017 Fungal Infectious Disease 54 1.819
356
PNC041 Pancreatic Ductal Adenocarcinoma 51 1.819
357
P RNV001 Renovascular Hypertension 49 1.811
358
OBS082 Obstructive Nephropathy 41 1.808
359
DBT006 Diabetic Macular Edema 48 1.808
360
VSC002 Vascular Dementia 60 1.808
361
P ENC004 Encephalitis 61 1.808
362
LYM019 Lymphosarcoma 46 1.808
363
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 52 1.757
364
PRS129 Prostatic Hyperplasia, Benign 49 1.755
365
SPP011 Suppression of Tumorigenicity 12 61 1.755
366
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 37 1.755
367
OST159 Osteogenic Sarcoma 66 1.755
368
P OPN001 Open-Angle Glaucoma 55 1.755
369
BLR008 Bilirubin Metabolic Disorder 57 1.755
370
PRS021 Prostatic Adenoma 43 1.755
371
PRS045 Prostatic Hypertrophy 53 1.755
372
CHR466 Chronic Thromboembolic Pulmonary Hypertension 48 1.755
373
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 70 1.745
374
P MYC084 Mycobacterium Tuberculosis 1 68 1.740
375
CHR710 Chronic Spontaneous Urticaria 45 1.733
376
HYP020 Hyperprolactinemia 63 1.733
377
ALL006 Allergic Asthma 56 1.733
378
P CHL066 Cholangitis 52 1.733
379
P ENC018 Encephalopathy 62 1.733
380
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 45 1.733
381
P PRS038 Personality Disorder 65 1.726
382
SCK003 Sickle Cell Anemia 74 1.711
383
P SCK005 Sickle Cell Disease 56 1.711
384
P ALP008 Alopecia 54 1.711
385
ANX010 Anxiety 70 1.689
386
P FML011 Familial Adenomatous Polyposis 71 1.689
387
P AMY004 Amyloidosis 70 1.689
388
HYP005 Hypokalemia 55 1.689
389
P MNC007 Monocytic Leukemia 47 1.689
390
HLX001 Helix Syndrome 48 1.689
391
OPP002 Opportunistic Mycosis 39 1.689
392
VLV011 Vulvovaginal Candidiasis 49 1.689
393
ORL005 Oral Candidiasis 56 1.689
394
c SYS043 Systemic Lupus Erythematosus 1 38 1.683
395
OBS002 Obsessive-Compulsive Disorder 68 1.653
396
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 46 1.653
397
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 1.644
398
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 1.633
399
WTH001 Withdrawal Disorder 48 1.618
400
MLD018 Mild Cognitive Impairment 48 1.618
401
c GLC092 Glaucoma, Primary Open Angle 62 1.618
402
LMY002 Leiomyoma 51 1.618
403
P STS003 Sitosterolemia 53 1.618
404
MYF001 Myofibroma 42 1.618
405
P LNG064 Lung Cancer Susceptibility 3 70 1.618
406
AMR003 Amaurosis Fugax 33 1.618
407
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 66 1.613
408
LYM040 Lymphoblastic Lymphoma 53 1.601
409
CTS005 Catastrophic Antiphospholipid Syndrome 43 1.601
410
CRY008 Cryopyrin-Associated Periodic Syndrome 48 1.601
411
P OVR042 Ovarian Cancer 88 1.565
412
ANL018 Analbuminemia 53 1.565
413
P LCH002 Lichen Planus 54 1.565
414
DBT010 Diabetic Neuropathy 54 1.565
415
CHG001 Chagas Disease 66 1.565
416
PLC002 Plica Syndrome 35 1.565
417
SYN007 Synovitis 55 1.565
418
P INF037 Inflammatory Bowel Disease 53 1.544
419
ATR057 Atrioventricular Block 54 1.544
420
PTN004 Patent Ductus Venosus 31 1.544
421
P SBR004 Seborrheic Dermatitis 44 1.544
422
P ART023 Arthropathy 61 1.544
423
LNG039 Lung Squamous Cell Carcinoma 57 1.544
424
P UVT001 Uveitis 57 1.544
425
P PST095 Post-Thrombotic Syndrome 51 1.544
426
RTN020 Retinal Vascular Disease 46 1.544
427
JPN002 Japanese Encephalitis 61 1.544
428
GST023 Gastric Ulcer 52 1.544
429
CRS001 Crescentic Glomerulonephritis 42 1.544
430
BCK003 Background Diabetic Retinopathy 47 1.544
431
DCB001 Decubitus Ulcer 62 1.544
432
SYS003 Systolic Heart Failure 49 1.544
433
CNG092 Congenital Extrahepatic Portosystemic Shunt 24 1.544
434
ATX019 Ataxia with Vitamin E Deficiency 44 1.522
435
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 40 1.508
436
THR100 Thrombocytopenic Purpura, Autoimmune 61 1.508
437
KRT002 Keratomalacia 55 1.508
438
P VSC018 Visceral Steatosis 32 1.508
439
c CHR064 Chronic Monocytic Leukemia 36 1.508
440
P NSP012 Nasopharyngeal Carcinoma 61 1.500
441
P SLP005 Sleep Disorder 61 1.500
442
P KDN017 Kidney Cancer 61 1.500
443
P RTN022 Retinal Vein Occlusion 54 1.500
444
DRG024 Drug Allergy 40 1.469
445
CRB086 Cerebral Aneurysms 40 1.469
446
CRD223 Cardiac Arrhythmia 63 1.463
447
c ATM099 Autoimmune Uveitis 45 1.463
448
c MYC058 Myocardial Infarction 2 24 1.463
449
P PSD087 Pseudoxanthoma Elasticum 67 1.463
450
ESP021 Esophageal Cancer 83 1.463
451
SKN016 Skin Disease 63 1.463
452
c FTL070 Fetal Akinesia Deformation Sequence 2 36 1.463
453
ALC010 Alcoholic Cardiomyopathy 42 1.463
454
CRN017 Coronary Thrombosis 46 1.463
455
P MYG005 Myoglobinuria 40 1.463
456
TTN003 Tetanus 65 1.463
457
CYS009 Cystadenoma 43 1.463
458
P ADL010 Adult Respiratory Distress Syndrome 71 1.463
459
ATN005 Autonomic Dysfunction 46 1.463
460
PRQ001 Paraquat Lung 16 1.463
461
c PRM038 Primary Agammaglobulinemia 47 1.460
462
HYP732 Hyperalphalipoproteinemia 1 52 1.421
463
CYS001 Cystic Fibrosis 78 1.397
464
MYL009 Myelodysplastic Syndrome 67 1.397
465
c HYP739 Hyperlipoproteinemia, Type Iv 53 1.397
466
PRD004 Prediabetes Syndrome 52 1.397
467
MTC005 Mitochondrial Metabolism Disease 45 1.386
468
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 46 1.386
469
ANX004 Anoxia 40 1.376
470
MTH086 Methotrexate Toxicity 32 1.376
471
P SCH015 Schizophrenia 74 1.376
472
THR099 Third-Degree Atrioventricular Block 42 1.376
473
c GRV008 Graves Disease 1 54 1.376
474
HMM004 Hamamy Syndrome 39 1.376
475
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 1.376
476
OST017 Osteomyelitis 63 1.376
477
HPT004 Hepatic Coma 43 1.376
478
ART012 Aortitis 42 1.376
479
BLP005 Blepharitis 50 1.376
480
P HMR005 Hemorrhoid 49 1.376
481
P ACN011 Acne 57 1.376
482
RTR001 Retrograde Amnesia 41 1.376
483
P INT070 Intestinal Obstruction 57 1.376
484
CHR096 Chronic Pulmonary Heart Disease 41 1.376
485
P GLL022 Guillain-Barre Syndrome 60 1.376
486
HPT019 Hepatic Encephalopathy 59 1.376
487
CRY003 Cryptosporidiosis 56 1.376
488
DRG002 Drug-Induced Hepatitis 42 1.376
489
HYD002 Hydronephrosis 58 1.376
490
CRT015 Carotid Artery Occlusion 45 1.376
491
SPT004 Septic Arthritis 58 1.376
492
EXT006 Extrahepatic Cholestasis 40 1.376
493
PLM010 Pulmonary Edema 55 1.376
494
P CMP008 Compartment Syndrome 50 1.376
495
P CRB088 Cerebral Atrophy 33 1.376
496
c CHR708 Chronic Urticaria 42 1.359
497
OST062 Osteoarthritis with Mild Chondrodysplasia 47 1.344
498
EPT021 Epithelial Recurrent Erosion Dystrophy 46 1.344
499
CMP010 Complex Regional Pain Syndrome 60 1.344
500
ARC025 Arachnoid Cysts, Intracranial 37 1.279
501
MDR006 Moderate and Severe Traumatic Brain Injury 27 1.279
502
c ACT134 Acute Liver Failure 59 1.279
503
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 1.279
504
VLV047 Volvulus of Midgut 52 1.279
505
CHL152 Childhood Acute Lymphocytic Leukemia 50 1.279
506
KRT019 Keratitis, Hereditary 66 1.279
507
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 1.279
508
HRN029 Hearing Loss, Noise-Induced 37 1.279
509
P PLM034 Pulmonary Emphysema 58 1.279
510
CMB007 Combined Immunodeficiency 57 1.279
511
ASP007 Aspiration Pneumonia 49 1.279
512
PLR008 Pleurisy 50 1.279
513
ACR007 Acromegaly 70 1.279
514
RTR008 Root Resorption 44 1.279
515
TRN018 Transitional Cell Carcinoma 56 1.279
516
GST033 Gestational Diabetes 61 1.279
517
BRN024 Bronchitis 67 1.279
518
P TRT010 Teratoma 51 1.279
519
NNC012 Non-Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency 17 1.279
520
DXR001 Doxorubicin Induced Cardiomyopathy 32 1.279
521
P HYP069 Hyperparathyroidism 62 1.276
522
c PNS012 Paine Syndrome 60 1.253
523
P BLD124 Bleeding Disorder, Platelet-Type, 11 67 1.253
524
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 54 1.253
525
c EPS039 Episodic Pain Syndrome, Familial, 1 42 1.253
526
PLY105 Polycystic Ovary Syndrome 1 39 1.253
527
P PRC031 Preeclampsia/eclampsia 1 43 1.253
528
SPR126 Superior Semicircular Canal Dehiscence 41 1.253
529
P ECL001 Eclampsia 52 1.253
530
P INT143 Interstitial Cystitis 60 1.253
531
MSC190 Muscular Disease 37 1.253
532
c HMG029 Hemoglobin Se Disease 40 1.253
533
LYM133 Lymphoma, Hodgkin, Classic 74 1.234
534
GLM044 Glomerular Disease 35 1.234
535
ART002 Arts Syndrome 66 1.234
536
KHL003 Kohlschutter-Tonz Syndrome 59 1.234
537
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 1.234
538
LYM143 Lymphoma, Non-Hodgkin, Familial 75 1.234
539
ART001 Arterial Tortuosity Syndrome 65 1.234
540
LYN004 Lynch Syndrome I 58 1.234
541
APR006 Apert Syndrome 70 1.234
542
BLD051 Blood Coagulation Disease 53 1.234
543
PLM001 Pulmonary Tuberculosis 69 1.234
544
P LYN001 Lynch Syndrome 76 1.234
545
PPL001 Papillary Adenoma 44 1.234
546
PLS009 Plasma Cell Neoplasm 64 1.234
547
CLC006 Calcinosis 47 1.234
548
ADS004 Aids Dementia Complex 40 1.234
549
CYT018 Cytochrome P450 2d6 Variant 26 1.234
550
ESN015 Eosinophilic Fasciitis 47 1.228
551
FSC004 Fasciitis 49 1.228
552
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 1.169
553
c GLL024 Gallbladder Disease 1 52 1.169
554
c STS010 Sitosterolemia 1 46 1.169
555
HLC007 Helicobacter Pylori Infection 67 1.169
556
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 1.169
557
MMM006 Mammographic Density 39 1.169
558
P CRT085 Carotid Intimal Medial Thickness 2 22 1.169
559
SKN019 Skin Melanoma 71 1.169
560
P FBR017 Fibrosarcoma 56 1.169
561
END040 Endogenous Depression 55 1.169
562
LNG099 Lung Disease 62 1.169
563
c STS011 Sitosterolemia 2 34 1.169
564
P HYD006 Hydrocephalus 61 1.169
565
QDR001 Quadriplegia 50 1.169
566
P MYC033 Myoclonus 47 1.169
567
PRS115 Prosthetic Joint Infection 42 1.169
568
SPS057 Spasticity 42 1.168
569
P CTN015 Cutaneous T Cell Lymphoma 48 1.160
570
c PSR028 Psoriasis 7 43 1.160
571
c PSR017 Psoriasis 2 53 1.160
572
c PSR018 Psoriasis 13 52 1.160
573
c PSR023 Psoriasis 1 52 1.160
574
c PSR032 Psoriasis 11 47 1.160
575
P MJR007 Major Affective Disorder 1 42 1.106
576
MYL031 Myeloproliferative Neoplasm 66 1.106
577
PST028 Post-Traumatic Stress Disorder 59 1.106
578
FBR089 Fibrosclerosis, Multifocal 35 1.090
579
P BLR024 Biliary Cirrhosis, Primary, 1 28 1.090
580
SMT004 Smith-Lemli-Opitz Syndrome 70 1.090
581
c MCL062 Mucolipidosis Ii Alpha/beta 68 1.090
582
DBT092 Diabetes Insipidus, Nephrogenic, X-Linked 38 1.090
583
END057 Endometrial Cancer 72 1.090
584
P PRP056 Porphyria, Acute Hepatic 49 1.090
585
CRH005 Crohn's Colitis 53 1.090
586
RNL065 Renal Cell Carcinoma, Papillary, 1 79 1.090
587
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 46 1.090
588
ACR041 Acromelic Frontonasal Dysostosis 53 1.090
589
c SRC023 Sarcoidosis 2 44 1.090
590
P SRC025 Sarcoidosis 1 71 1.090
591
c INF071 Inflammatory Bowel Disease 1 65 1.090
592
P GLM040 Glioma Susceptibility 1 71 1.090
593
NRR001 Neuroretinitis 42 1.090
594
RTN023 Retinitis 46 1.090
595
c BRS049 Breast Carcinoma in Situ 50 1.090
596
CVR006 Cavernous Hemangioma 51 1.090
597
HMT002 Hematologic Cancer 61 1.090
598
VSL013 Visual Impairment and Progressive Phthisis Bulbi 36 1.090
599
PLM012 Pulmonary Sarcoidosis 53 1.090
600
BLD053 Blood Platelet Disease 51 1.090
601
c INF023 Inflammatory Breast Carcinoma 49 1.090
602
P EYD002 Eye Disease 57 1.090
603
BRS099 Breast Ductal Carcinoma 61 1.090
604
P CPL006 Capillary Hemangioma 53 1.090
605
CRN006 Coronary Aneurysm 41 1.090
606
DFF003 Diffuse Scleroderma 41 1.090
607
IRN002 Iron Metabolism Disease 57 1.090
608
ACT113 Acute Myeloblastic Leukemia with Maturation 46 1.090
609
MST020 Mast Cell Activation Syndrome 28 1.090
610
RTR011 Retroperitoneal Fibrosis 47 1.090
611
c CHR417 Chronic Graft Versus Host Disease 55 1.090
612
NPH091 Nephrolithiasis, Calcium Oxalate 61 1.085
613
P RHB003 Rhabdomyosarcoma 66 1.085
614
TRC022 Tricuspid Valve Insufficiency 47 1.085
615
NPH009 Nephrolithiasis 54 1.085
616
c HRD010 Hereditary Spastic Paraplegia 66 1.059
617
P VNW001 Von Willebrand's Disease 65 1.058
618
CHR603 Chronic Enteropathy Associated with Slco2a1 Gene 25 1.043
619
c EHL080 Ehlers-Danlos Syndrome, Musculocontractural Type, 1 52 1.043
620
CMR002 Coumarin Resistance 59 1.043
621
CRV035 Cervical Cancer 73 1.038
622
c FNC027 Fanconi Anemia, Complementation Group a 81 1.038
623
MTB004 Metabolic Acidosis 48 1.038
624
TND006 Tendinosis 41 1.038
625
c FNC042 Fanconi Anemia, Complementation Group D2 54 1.038
626
HPT022 Hepatoblastoma 54 1.038
627
CHL067 Cholecystitis 60 1.038
628
PHG002 Phagocyte Bactericidal Dysfunction 34 1.038
629
ESP023 Esophageal Disease 52 1.038
630
INT066 Interstitial Lung Disease 60 1.038
631
PLG002 Plague 58 1.038
632
DBT004 Diabetic Polyneuropathy 50 1.038
633
ANC002 Anca-Associated Vasculitis 44 1.038
634
LNR006 Linear Iga Disease 40 1.038
635
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 1.005
636
P PRK057 Parkinson Disease, Late-Onset 80 1.005
637
CRB008 Cerebral Atherosclerosis 46 0.950
638
INT074 Intracranial Arteriosclerosis 22 0.950
639
PSR001 Psoriatic Arthritis 62 0.928
640
END062 Endometrial Hyperplasia 48 0.917
641
URM002 Uremia 47 0.917
642
P ORF001 Orofaciodigital Syndrome 50 0.906
643
PMP009 Pemphigus Erythematosus 29 0.868
644
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.868
645
BRK010 Burkitt Lymphoma 66 0.868
646
TLM001 Telomere Length, Mean Leukocyte 16 0.868
647
HMR023 Hemorrhagic Cystitis 43 0.868
648
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.868
649
KRN002 Kearns-Sayre Syndrome 63 0.868
650
c PRG020 Paragangliomas 3 39 0.868
651
P HRD008 Hereditary Hemorrhagic Telangiectasia 65 0.868
652
ART010 Arteriolosclerosis 37 0.868
653
P PMP001 Pemphigus 55 0.868
654
INT075 Intracranial Hypertension 53 0.868
655
P CYS018 Cystitis 59 0.868
656
TLN003 Telangiectasis 51 0.868
657
CRY005 Cryptococcosis 60 0.868
658
CHL014 Cholera 62 0.868
659
SCH014 Schistosomiasis 56 0.868
660
P MYS079 Miyoshi Muscular Dystrophy 54 0.868
661
MNN009 Meningoencephalitis 48 0.868
662
P INF032 Infertility 57 0.868
663
PLS007 Plasmodium Falciparum Malaria 52 0.868
664
MNN002 Mononeuritis Multiplex 38 0.868
665
LCH013 Lichen Planus Pemphigoides 33 0.868
666
MSC007 Muscle Hypertrophy 64 0.840
667
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.840
668
c HYP843 Hypoalphalipoproteinemia, Primary, 2 50 0.840
669
ACT017 Acute Chest Syndrome 50 0.840
670
P PHC003 Pheochromocytoma 69 0.820
671
LMB062 Limb Ischemia 55 0.820
672
APH002 Aphasia 56 0.820
673
c CRB191 Cerebral Cavernous Malformations 2 45 0.820
674
c CRB094 Cerebral Cavernous Malformations 3 41 0.820
675
TBC004 Tobacco Addiction 63 0.820
676
HRW001 Hair Whorl 35 0.820
677
ADR040 Adrenal Gland Pheochromocytoma 46 0.820
678
ACT003 Acute Kidney Tubular Necrosis 46 0.820
679
P EMB005 Embryonal Rhabdomyosarcoma 53 0.820
680
NRM001 Neuromyelitis Optica 61 0.820
681
MCR141 Mucormycosis 59 0.820
682
CHL147 Chlamydia Pneumonia 47 0.820
683
P ANG015 Angioedema 56 0.820
684
FCL012 Facial Paralysis 49 0.820
685
P GLY013 Glycogen Storage Disease 60 0.820
686
CHL123 Chlamydia 58 0.820
687
P RTN018 Retinal Disease 53 0.820
688
P BNG032 Benign Mesothelioma 53 0.820
689
CND006 Candida Glabrata 30 0.820
690
P OVR082 Overgrowth Syndrome 49 0.758
691
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 58 0.758
692
P ANT001 Anterolateral Myocardial Infarction 34 0.758
693
P ESP024 Esophagitis 60 0.758
694
P TRC086 Trichohepatoenteric Syndrome 1 59 0.742
695
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.742
696
LPT006 Leptin Receptor Deficiency 50 0.742
697
P NJM001 Nijmegen Breakage Syndrome 76 0.742
698
ATY005 Atypical Teratoid Rhabdoid Tumor 69 0.742
699
DDN006 Duodenitis 50 0.742
700
ACR039 Acromegaloid Hypertrichosis Syndrome 23 0.742
701
GLY081 Glycogen Storage Disease Due to Glucose-6-Phosphatase Deficiency 47 0.710
702
P LPR021 Leprosy 3 71 0.710
703
MYC006 Mycosis Fungoides 65 0.710
704
CRT045 Creatine Phosphokinase, Elevated Serum 39 0.710
705
GRN037 Granulomatosis with Polyangiitis 64 0.710
706
ATS010 Autosomal Recessive Disease 42 0.710
707
BRR014 Barrett Esophagus 66 0.710
708
AST006 Astigmatism 47 0.710
709
ACT119 Acute Promyelocytic Leukemia 62 0.710
710
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 0.710
711
c GLY060 Glycogen Storage Disease Ia 63 0.710
712
VRC005 Varicose Veins 60 0.710
714
INT067 Interstitial Nephritis 46 0.710
715
P MYP006 Myopia 56 0.710
716
P MSC003 Muscular Atrophy 52 0.710
717
P MLG056 Malignant Hyperthermia 66 0.710
718
P VND001 Vein Disease 42 0.710
719
ADG002 Audiogenic Seizures 25 0.710
720
P VNT002 Ventricular Septal Defect 58 0.710
721
PNC129 Pancreatic Adenocarcinoma 65 0.710
722
INS001 Insulinoma 59 0.710
723
PPT005 Peptic Ulcer Disease 58 0.710
724
SBC019 Subcutaneous Mycosis 35 0.710
725
SPR010 Sporotrichosis 46 0.710
726
HGH043 High Grade Glioma 45 0.710
727
P BND020 Bone Disease 59 0.710
728
HMP005 Hemiplegia 54 0.710
729
PRS025 Presbyopia 38 0.710
730
DSS009 Disseminated Intravascular Coagulation 57 0.710
731
P PRN023 Prion Disease 60 0.710
732
HNS001 Hansen's Disease 32 0.710
733
CRB090 Cerebral Hypoxia 42 0.710
734
FRS019 Farsightedness 36 0.710
735
DYS073 Dysphagia 53 0.710
736
ALN001 Aland Island Eye Disease 55 0.696
737
P CNR004 Cone-Rod Dystrophy 2 74 0.696
738
HYP781 Hypoascorbemia 52 0.696
739
c LKM063 Leukemia, Chronic Myeloid 71 0.696
740
MNT001 Mantle Cell Lymphoma 67 0.696
741
LYM012 Lymphoplasmacytic Lymphoma 50 0.696
742
WLD007 Waldenstroem's Macroglobulinemia 63 0.696
743
RHM028 Rheumatic Heart Disease 56 0.696
744
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 0.696
745
c MSM022 Mismatch Repair Cancer Syndrome 1 70 0.696
746
c FCL025 Focal Segmental Glomerulosclerosis 1 49 0.696
747
c HYP841 Hypoalphalipoproteinemia, Primary, 1 49 0.696
748
c MJR006 Major Affective Disorder 5 32 0.696
749
c MJR023 Major Affective Disorder 7 33 0.696
750
c MJR004 Major Affective Disorder 4 28 0.696
751
c MJR003 Major Affective Disorder 6 32 0.696
752
c MJR008 Major Affective Disorder 2 34 0.696
753
SLT014 Salt and Pepper Developmental Regression Syndrome 43 0.696
754
BHR001 Behr Syndrome 51 0.696
755
CRD220 Cardiac Valvular Defect, Developmental 28 0.696
756
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 69 0.696
757
MCR004 Macroglobulinemia 49 0.696
758
INT003 Intracranial Hypotension 36 0.696
759
BNM001 Bone Marrow Cancer 46 0.696
760
MYL075 Myelodysplastic/myeloproliferative Neoplasm 51 0.696
761
VRL011 Viral Infectious Disease 61 0.696
763
LNG031 Lung Benign Neoplasm 51 0.696
764
ACT084 Acute Stress Disorder 54 0.696
765
EBL001 Ebola Hemorrhagic Fever 56 0.696
766
CHR546 Chronic Mountain Sickness 43 0.696
767
OST003 Osteonecrosis 61 0.696
768
PRL017 Prolymphocytic Leukemia 47 0.696
769
SCN001 Secondary Hyperparathyroidism of Renal Origin 24 0.696
770
c SCN007 Secondary Hyperparathyroidism 51 0.696
771
LCH001 Leech Infestation 38 0.696
772
P ACT105 Acute Mountain Sickness 52 0.696
773
P CLL015 Collagen Disease 48 0.696
774
ATM021 Autoimmune Inner Ear Disease 36 0.696
775
ANG011 Angiodysplasia 42 0.648
776
BCK006 Back Pain 47 0.648
777
CLC053 Colchicine Poisoning 23 0.580
778
PRN061 Prenatal-Onset Spinal Muscular Atrophy with Congenital Bone Fractures 13 0.580
779
P VTR007 Vitreoretinopathy 46 0.580
780
P THL005 Thalassemia 56 0.580
781
TNG002 Tangier Disease 64 0.580
782
RTN017 Retinal Detachment 60 0.580
783
FCT001 Factor Viii Deficiency 60 0.580
784
c MST023 Mesothelioma, Malignant 56 0.580
785
c BTT014 Beta-Thalassemia 72 0.580
786
INF034 Infective Endocarditis 54 0.580
787
SXL003 Sexual Disorder 49 0.580
788
BTT017 Beta-Thalassemia Major 51 0.580
789
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.580
790
c HMP029 Hemophilia a 68 0.580
791
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 65 0.580
792
PLY001 Polycythemia Vera 69 0.580
793
SPR004 Supravalvular Aortic Stenosis 57 0.580
794
VTR016 Vater/vacterl Association 49 0.580
795
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.580
796
URT049 Urate Oxidase, Pseudogene 24 0.580
797
P HNT016 Huntington Disease 73 0.580
798
DSS032 Disease by Infectious Agent 55 0.580
799
CHR431 Chronic Venous Insufficiency 48 0.580
800
SCR011 Scrapie 39 0.580
801
P CHR012 Chronic Granulomatous Disease 69 0.580
802
CLL003 Cellulitis 53 0.580
803
P LCT001 Lactic Acidosis 51 0.580
804
LYM027 Lymphopenia 56 0.580
805
FBR047 Fibromyalgia 58 0.580
806
P CTR002 Cataract 60 0.580
807
P PLY018 Polycythemia 56 0.580
808
P MMB011 Membranous Nephropathy 50 0.580
809
P VNS003 Venous Insufficiency 55 0.580
810
HPT085 Hepatitis, Fulminant Viral 33 0.580
811
P DNG005 Dengue Virus 56 0.580
812
CRN019 Coronary Artery Vasospasm 47 0.580
813
PNC001 Pancytopenia 53 0.580
814
EPC002 Epicondylitis 44 0.580
815
RYS001 Reye Syndrome 49 0.580
816
PRT014 Protein S Deficiency 41 0.580
817
DBT008 Diabetic Angiopathy 45 0.580
818
P MCR010 Microcephaly 60 0.580
819
HMP001 Hemopericardium 47 0.580
820
P PRC012 Pericardial Effusion 50 0.580
821
P END033 Endocarditis 58 0.580
822
P RHN004 Rhinitis 57 0.580
823
P HYP076 Hyperthyroidism 53 0.580
824
ACT058 Active Peptic Ulcer Disease 56 0.580
825
P THR015 Thrombophilia 51 0.580
826
PTN001 Patent Foramen Ovale 62 0.580
827
VCT001 Vacterl Association 47 0.580
828
P HMP007 Hemophilia 52 0.580
829
BRK012 Broken Heart Syndrome 42 0.580
830
P PRD037 Periodontal Ehlers-Danlos Syndrome 49 0.580
831
RNL001 Renal Artery Obstruction 31 0.492
832
SLR005 Solar Urticaria 29 0.458
833
MCR037 Macroglossia 44 0.458
834
HMN047 Human Cytomegalovirus Infection 57 0.458
835
HPT025 Hepatic Lipase Deficiency 47 0.458
836
FXD003 Fixed Drug Eruption 34 0.458
837
P MLN007 Male Infertility 56 0.458
838
BRN012 Bronchiolitis Obliterans 56 0.458
839
BRN002 Bronchiolitis 57 0.458
840
HDR003 Hidradenitis 50 0.458
841
LYS003 Lysinuric Protein Intolerance 57 0.410
842
c SBC035 Subacute Cutaneous Lupus Erythematosus 34 0.410
843
ADR022 Adrenomyeloneuropathy 39 0.410
844
SRT004 Serotonin Syndrome 54 0.410
845
DFF031 Diffuse Alveolar Hemorrhage 31 0.410
846
ATR055 Atrial Septal Aneurysm 23 0.410
847
LYS029 Lysosomal Disease 30 0.410
848
THR123 Thrombotic Microangiopathy 40 0.410
849
c DWL002 Dowling-Degos Disease 1 58 0.410
850
P FML018 Familial Mediterranean Fever 73 0.410
851
ALL003 Allergic Rhinitis 67 0.410
852
P SPR120 Supranuclear Palsy, Progressive, 1 69 0.410
853
BDD001 Budd-Chiari Syndrome 62 0.410
854
c RTN047 Retinitis Pigmentosa 18 46 0.410
855
XNT003 Xanthomatosis 49 0.410
856
P DRM053 Dermatitis, Atopic 65 0.410
857
BRT054 Brittle Bone Disorder 74 0.410
858
c LKM070 Leukemia, Acute Monocytic 56 0.410
859
LPM012 Lipomatosis, Multiple 60 0.410
860
ANS021 Anisocoria 25 0.410
861
P TMP003 Temporal Arteritis 69 0.410
862
HYP457 Hypertrophic Scars 42 0.410
863
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.410
865
P MCL001 Mucolipidosis 49 0.410
866
c BNG093 Benign Teratoma 39 0.410
867
P ERY036 Erythema Nodosum 49 0.410
868
c ATS007 Autism Spectrum Disorder 72 0.410
869
P LYM033 Lymphoproliferative Syndrome 59 0.410
870
HPT046 Hepatic Veno-Occlusive Disease 62 0.410
871
P SML001 Small Cell Carcinoma 52 0.410
872
MLT180 Multisystem Inflammatory Syndrome in Children 32 0.410
873
P TRN034 Transverse Myelitis 47 0.410
874
CRB011 Cerebrotendinous Xanthomatosis 65 0.410
875
WRN001 Werner Syndrome 69 0.410
876
LYS012 Lysosomal Acid Lipase Deficiency 65 0.410
877
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.410
878
NRL016 Neural Tube Defects 81 0.410
879
CNT105 Central Core Disease of Muscle 59 0.410
880
LNG108 Langerhans Cell Histiocytosis 58 0.410
881
P GST053 Gastric Cancer 83 0.410
882
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.410
883
MYP071 Myopathy Due to Myoadenylate Deaminase Deficiency 43 0.410
884
LPP002 Lipoprotein Glomerulopathy 43 0.410
885
AFB002 Afibrinogenemia, Congenital 64 0.410
886
CYS013 Cystinuria 66 0.410
887
P SPP010 Suppressor of Tumorigenicity 3 51 0.410
888
LCH016 Lichen Sclerosus Et Atrophicus 42 0.410
889
HMF008 Hemifacial Atrophy, Progressive 38 0.410
890
PRD013 Periodic Fever, Familial, Autosomal Dominant 68 0.410
891
c HRM017 Hermansky-Pudlak Syndrome 2 55 0.410
892
EST002 Estrogen-Receptor Negative Breast Cancer 45 0.410
893
c NMN016 Niemann-Pick Disease, Type B 56 0.410
894
P FLL037 Follicular Lymphoma 74 0.410
895
CRD137 Cardiogenic Shock 56 0.410
897
RRC033 Rare Coagulation Disorder 11 0.410
898
c PST005 Posterior Uveitis 54 0.410
899
PMP014 Pemphigoid 51 0.410
900
P HRD214 Hereditary Periodic Fever Syndrome 30 0.410
901
P HYP083 Hypopituitarism 52 0.410
902
AVN001 Avian Influenza 61 0.410
903
SCH012 Schizoaffective Disorder 50 0.410
904
P HMC002 Homocystinuria 53 0.410
905
CRT008 Carotid Artery Dissection 29 0.410
906
c BCT013 Bacterial Pneumonia 48 0.410
907
P MTC133 Mitochondrial Myopathy 50 0.410
908
SPN185 Spinal Cord Infarction 28 0.410
909
PST092 Posttransplant Acute Limbic Encephalitis 28 0.410
910
P ALP009 Alopecia Areata 59 0.410
911
SPC030 Specific Language Disorder 25 0.410
912
ANR004 Anuria 44 0.410
913
P ANT006 Antiphospholipid Syndrome 55 0.410
914
NRN001 Neuroendocrine Carcinoma 47 0.410
915
P OPT006 Optic Nerve Disease 58 0.410
916
HST010 Histiocytosis 49 0.410
917
P SKN015 Skin Carcinoma 71 0.410
918
CHL050 Cholesterol Ester Storage Disease 31 0.410
919
CHL070 Cholesterol Embolism 39 0.410
920
OVR063 Overnutrition 42 0.410
921
INF013 Inferior Myocardial Infarction 33 0.410
922
MYL001 Myelitis 50 0.410
923
FCL003 Facial Hemiatrophy 29 0.410
924
BLL006 Bullous Pemphigoid 61 0.410
925
PHN011 Phenytoin Toxicity 32 0.410
926
ASY002 Asymptomatic Neurosyphilis 41 0.410
927
PLM005 Pleomorphic Lipoma 40 0.410
928
P HMP002 Hemophagocytic Lymphohistiocytosis 61 0.410
929
P CTN003 Cutaneous Lupus Erythematosus 52 0.410
930
ERY003 Erythema Multiforme 56 0.410
931
P MGR001 Migraine Without Aura 49 0.410
932
P GRV001 Graves' Disease 55 0.410
933
P OPT009 Optic Neuritis 57 0.410
934
PCD001 Pica Disease 38 0.410
935
SBC014 Subclavian Steal Syndrome 31 0.410
936
PPL022 Papilloma 53 0.410
937
SQM002 Squamous Cell Papilloma 46 0.410
938
P NMN002 Niemann-Pick Disease 60 0.410
939
EXS001 Exostosis 49 0.410
940
P GCH001 Gaucher's Disease 70 0.410
941
CNT016 Central Retinal Vein Occlusion 54 0.410
942
P CYS017 Cystic Teratoma 41 0.410
943
P LNG028 Long Qt Syndrome 64 0.410
944
DPH001 Diphtheria 59 0.410
945
P RNL015 Renal Hypertension 45 0.410
946
BRC012 Brucellosis