Search results for Aspirin

2315 hits were found for Aspirin

# Family MCID Name MIFTS Score
1
AST052 Asthma, Nasal Polyps, and Aspirin Intolerance 42 53.975
2
ASP030 Aspirin Resistance 41 51.026
3
ASP038 Aspirin-Induced Respiratory Disease 16 29.916
4
ASP036 Aspirin Allergy 28 26.304
5
LPP008 Lipoprotein Quantitative Trait Locus 65 20.015
6
ART140 Arteries, Anomalies of 52 19.714
7
ISC004 Ischemia 61 16.868
8
STR067 Stroke, Ischemic 79 16.532
9
c PRC016 Pre-Eclampsia 64 16.106
10
P CRN300 Coronary Heart Disease 1 73 16.002
11
CRB039 Cerebrovascular Disease 65 14.812
12
TRN015 Transient Cerebral Ischemia 62 13.694
13
P VSC007 Vascular Disease 62 13.535
14
P MYC007 Myocardial Infarction 69 13.334
15
c THR092 Thrombophilia Due to Thrombin Defect 74 13.157
16
INT007 Intermediate Coronary Syndrome 53 12.561
17
PPT005 Peptic Ulcer Disease 58 12.419
18
PRP027 Peripheral Vascular Disease 71 11.859
19
P ATR011 Atrial Fibrillation 66 11.827
20
THR024 Thrombosis 56 11.705
21
P ECL001 Eclampsia 52 11.700
22
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 11.560
23
P CLR023 Colorectal Cancer 100 11.332
24
c ACT075 Acute Myocardial Infarction 55 11.237
25
ALL029 Allergic Disease 61 10.735
26
P HRT032 Heart Disease 84 10.118
27
ATH013 Atherosclerosis Susceptibility 63 9.987
28
c TYP009 Type 2 Diabetes Mellitus 91 9.858
29
PLM033 Pulmonary Embolism 58 9.634
30
P ANT006 Antiphospholipid Syndrome 55 9.493
31
P URT039 Urticaria 57 9.478
32
GST023 Gastric Ulcer 52 9.373
33
PRP080 Peripheral Artery Disease 54 9.308
34
PLT019 Platelet Disorder, Familial, with Associated Myeloid Malignancy 40 9.197
35
P DBT009 Diabetes Mellitus 67 9.154
36
P AST005 Asthma 75 9.108
37
c HYP724 Hyperlipoproteinemia, Type Iii 66 8.823
38
KWS002 Kawasaki Disease 65 8.766
39
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 8.684
40
ADN018 Adenoma 58 8.615
41
P CRD246 Cardiovascular System Disease 55 8.569
42
ANG054 Angina Pectoris 65 8.257
43
ACT058 Active Peptic Ulcer Disease 55 8.212
44
CLR108 Colorectal Adenoma 63 7.992
45
P RHN004 Rhinitis 56 7.901
46
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 7.411
47
c MGR028 Migraine with or Without Aura 1 63 7.204
48
CLP006 Clopidogrel Resistance 44 7.009
49
CRH001 Crohn's Disease 80 6.994
50
P DDN001 Duodenal Ulcer 52 6.963
51
P ESS003 Essential Thrombocythemia 68 6.922
52
P ANG015 Angioedema 56 6.878
53
CRT013 Carotid Stenosis 51 6.813
54
LPD008 Lipid Metabolism Disorder 61 6.796
55
RYS001 Reye Syndrome 49 6.702
56
ANR040 Aneurysm 60 6.567
57
c HYP595 Hypertension, Essential 84 6.364
58
c CHR684 Chronic Kidney Disease 73 6.302
59
c HYP836 Hypercholesterolemia, Familial, 1 73 6.220
60
P THR014 Thrombocytopenia 66 6.130
61
P PRS040 Prostate Cancer 95 5.992
62
CRN017 Coronary Thrombosis 46 5.932
63
P HDC001 Headache 56 5.925
64
CNG034 Congestive Heart Failure 69 5.862
65
P KDN018 Kidney Disease 71 5.854
66
P THR015 Thrombophilia 51 5.796
67
HLC007 Helicobacter Pylori Infection 67 5.563
68
LMB062 Limb Ischemia 55 5.521
69
P GST044 Gastritis 55 5.504
70
48X005 48,xyyy 39 5.435
71
THR004 Thrombocytosis 52 5.347
72
P BRS047 Breast Cancer 97 5.282
73
P RSP003 Respiratory Failure 73 5.278
74
CMM005 Common Cold 55 5.206
75
P PLY018 Polycythemia 56 5.091
76
PLY001 Polycythemia Vera 69 5.023
77
P ESP024 Esophagitis 60 4.964
78
PLC008 Placenta Disease 48 4.924
79
c BLD140 Blood Group, I System 47 4.919
80
INT002 Intermittent Claudication 61 4.917
81
P TRN020 Turner Syndrome 67 4.879
82
P HPT023 Hepatocellular Carcinoma 95 4.875
83
P LYN001 Lynch Syndrome 76 4.846
84
P ART021 Arteriosclerosis 53 4.839
85
P OVR042 Ovarian Cancer 88 4.835
86
P RHM011 Rheumatoid Arthritis 81 4.770
87
P GST053 Gastric Cancer 82 4.754
88
P ADL010 Adult Respiratory Distress Syndrome 70 4.751
89
ANT039 Antisynthetase Syndrome 55 4.728
90
OST012 Osteoarthritis 77 4.709
91
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 4.680
92
P CTR002 Cataract 59 4.635
93
ESP021 Esophageal Cancer 84 4.629
94
c SYS001 Systemic Lupus Erythematosus 85 4.623
95
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 4.617
96
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 4.617
97
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 4.617
98
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 4.617
99
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 4.617
100
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 4.617
101
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 4.617
102
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 4.617
103
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 4.617
104
PLC007 Placental Abruption 47 4.567
105
P BLD124 Bleeding Disorder, Platelet-Type, 11 68 4.507
106
PLM129 Pulmonary Disease, Chronic Obstructive 74 4.504
107
P PRD008 Periodontitis 63 4.500
108
c CHR708 Chronic Urticaria 42 4.494
109
P RCT021 Rectum Cancer 54 4.493
110
P PNC035 Pancreatic Cancer 87 4.484
111
P LNG032 Lung Cancer 98 4.482
112
INT030 Intracranial Aneurysm 55 4.450
114
P PRG092 Pregnancy Loss, Recurrent 1 42 4.362
115
P EXN002 Exanthem 58 4.356
116
P LPS004 Lupus Erythematosus 61 4.348
117
BRR014 Barrett Esophagus 66 4.299
118
PNG002 Pain Agnosia 51 4.257
119
P ADN016 Adenocarcinoma 63 4.240
120
P HYP098 Hypereosinophilic Syndrome 66 4.184
121
IGR001 Ige Responsiveness, Atopic 58 4.165
122
c MCR115 Microvascular Complications of Diabetes 5 65 4.165
123
P ANR048 Aniridia 1 66 4.163
124
GST092 Gastroesophageal Reflux 59 4.162
125
CVD001 Covid-19 59 4.105
126
ENT004 Enthesopathy 51 4.081
127
PRT251 Proteinuria, Chronic Benign 58 4.061
128
RHB024 Rhabdomyosarcoma 2 65 3.997
129
P ART022 Arthritis 70 3.976
130
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 37 3.956
131
CRN030 Coronary Stenosis 50 3.944
132
P PRC031 Preeclampsia/eclampsia 1 43 3.937
133
c SVR005 Severe Pre-Eclampsia 49 3.900
134
ADL002 Adult Syndrome 69 3.891
135
MYL069 Myeloma, Multiple 76 3.869
136
ALL003 Allergic Rhinitis 66 3.842
137
P CRN074 Coronary Artery Aneurysm 41 3.834
138
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 3.807
139
AGN016 Aging 53 3.798
140
PRP030 Purpura 54 3.759
141
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 3.751
142
CRB086 Cerebral Aneurysms 40 3.729
143
c PNS012 Paine Syndrome 60 3.705
144
c EPS039 Episodic Pain Syndrome, Familial, 1 42 3.705
145
PTN001 Patent Foramen Ovale 61 3.652
146
CRB009 Cerebritis 43 3.642
147
MYL031 Myeloproliferative Neoplasm 66 3.621
148
END057 Endometrial Cancer 76 3.584
149
c BRN108 Branchiootic Syndrome 1 63 3.539
150
END086 End Stage Renal Disease 54 3.492
151
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 3.491
152
P FML011 Familial Adenomatous Polyposis 70 3.491
153
P PNM007 Pneumonia 64 3.491
154
ALL006 Allergic Asthma 55 3.443
155
RPD005 Rapidly Involuting Congenital Hemangioma 48 3.438
156
TBR011 Tuberculous Meningitis 48 3.434
157
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 3.403
158
P BPL003 Bipolar Disorder 56 3.403
159
P MNN013 Meningitis 65 3.402
160
END072 Endotheliitis 36 3.400
161
c MJR022 Major Affective Disorder 8 37 3.398
162
c MJR024 Major Affective Disorder 9 40 3.398
163
DPR016 Depression 64 3.369
164
P VSC011 Vasculitis 61 3.359
165
PRC013 Pericarditis 53 3.350
166
DDN006 Duodenitis 49 3.332
167
CLN015 Colon Adenocarcinoma 64 3.326
168
DSS009 Disseminated Intravascular Coagulation 56 3.319
169
MNT002 Mental Depression 56 3.316
170
c FML001 Familial Atrial Fibrillation 65 3.311
171
P CNJ013 Conjunctivitis 66 3.307
172
TRM010 Traumatic Brain Injury 50 3.285
173
P MLN008 Melanoma 75 3.280
174
P DMN002 Dementia 65 3.264
175
P INF032 Infertility 60 3.258
176
VSC002 Vascular Dementia 59 3.220
177
P LVR013 Liver Disease 68 3.193
178
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 3.189
179
P MLT020 Multiple Sclerosis 79 3.179
180
CYT002 Cytokine Deficiency 43 3.161
181
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 3.153
182
RCK004 Rickets 64 3.148
183
INF034 Infective Endocarditis 53 3.143
184
P RTN022 Retinal Vein Occlusion 54 3.130
185
c SML038 Small Cell Cancer of the Lung 68 3.129
186
PRT013 Portal Hypertension 59 3.115
187
P PLM037 Pulmonary Hypertension 69 3.112
188
P BLD134 Bladder Cancer 79 3.079
189
TXC005 Toxic Shock Syndrome 61 3.069
191
RHM001 Rheumatic Fever 59 3.058
192
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 3.051
193
GST033 Gestational Diabetes 60 3.051
194
P KDN017 Kidney Cancer 60 3.038
195
PRT018 Portal Vein Thrombosis 50 3.029
196
CRB004 Cerebral Artery Occlusion 45 3.024
197
RSP006 Respiratory System Disease 51 3.006
198
RHM028 Rheumatic Heart Disease 55 3.005
199
PLC005 Placental Insufficiency 55 3.004
200
CRT016 Carotid Artery Disease 52 2.986
201
P SCK005 Sickle Cell Disease 56 2.965
203
SVR001 Severe Acute Respiratory Syndrome 68 2.897
204
PPT001 Peptic Esophagitis 51 2.890
205
LVR012 Liver Cirrhosis 62 2.888
206
ART002 Arts Syndrome 66 2.887
207
c MCR113 Microvascular Complications of Diabetes 3 52 2.880
208
c MCR133 Microvascular Complications of Diabetes 4 41 2.876
209
c MCR130 Microvascular Complications of Diabetes 6 41 2.876
210
c MCR120 Microvascular Complications of Diabetes 7 47 2.876
211
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 2.875
212
c TYP008 Type 1 Diabetes Mellitus 77 2.871
213
KRT002 Keratomalacia 54 2.865
214
HYP066 Hyperglycemia 60 2.857
215
GLB002 Glioblastoma 67 2.847
216
FTT001 Fatty Liver Disease 61 2.841
217
DFC004 Deficiency Anemia 74 2.833
218
CRN006 Coronary Aneurysm 41 2.827
219
P END033 Endocarditis 58 2.813
220
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 2.798
221
P SKN015 Skin Carcinoma 71 2.792
222
GSG001 Gas Gangrene 52 2.767
223
c PLM164 Pulmonary Hypertension, Primary, 1 75 2.753
224
P NTR004 Neutropenia 62 2.743
225
CRD137 Cardiogenic Shock 56 2.727
226
P MYC084 Mycobacterium Tuberculosis 1 68 2.709
227
EXR007 Exercise-Induced Anaphylaxis 24 2.705
228
CLT003 Colitis 63 2.702
229
47X002 47,xyy 47 2.702
230
P ALC033 Alcohol Use Disorder 67 2.672
231
P VNW001 Von Willebrand's Disease 64 2.657
232
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 2.633
233
CHC001 Chickenpox 56 2.626
234
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 2.625
235
c PRD040 Periodontitis, Chronic 52 2.624
236
OST062 Osteoarthritis with Mild Chondrodysplasia 46 2.624
237
PRS047 Prostatitis 57 2.611
238
BCK006 Back Pain 43 2.605
239
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 2.605
240
NNL005 Non-Alcoholic Fatty Liver Disease 63 2.602
241
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 2.575
242
P PST095 Post-Thrombotic Syndrome 51 2.567
243
c ACT249 Acute Asthma 40 2.565
244
BRN071 Brain Injury 50 2.564
245
P ERY008 Erythromelalgia 50 2.564
246
GST039 Gastroduodenitis 37 2.555
247
MCS002 Mucositis 55 2.551
248
HMR039 Hemorrhage, Intracerebral 57 2.538
249
CLN044 Colon Adenoma 44 2.533
250
HYP014 Hyperuricemia 51 2.522
251
STR039 Sturge-Weber Syndrome 60 2.514
252
SQM006 Squamous Cell Carcinoma 59 2.513
253
P SCH015 Schizophrenia 74 2.503
254
MCR011 Microinvasive Gastric Cancer 41 2.494
255
GT001 Gout 63 2.491
256
CHR710 Chronic Spontaneous Urticaria 45 2.477
257
P DRM053 Dermatitis, Atopic 65 2.476
258
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 2.466
259
TNS005 Tonsillitis 57 2.449
260
MYL005 Myelofibrosis 70 2.439
261
OCL069 Ocular Motor Apraxia 57 2.436
262
LYN004 Lynch Syndrome I 60 2.436
263
P SZR006 Seizure Disorder 69 2.425
264
P PNC044 Pancreatitis 61 2.406
265
INT040 Intrinsic Asthma 36 2.404
266
NRL005 Neurilemmoma 60 2.400
267
ACS001 Acoustic Neuroma 55 2.393
268
PPL001 Papillary Adenoma 44 2.389
269
PRT036 Peritonitis 65 2.379
270
c ART115 Aortic Valve Disease 1 72 2.377
271
CHR048 Chronic Rhinitis 46 2.377
272
P ART018 Aortic Valve Insufficiency 52 2.377
273
P FNG006 Feingold Syndrome 1 61 2.373
274
DWN001 Down Syndrome 70 2.371
275
P NRP001 Neuropathy 59 2.368
276
PHR003 Pharyngitis 57 2.367
277
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 2.364
278
OVR094 Ovarian Epithelial Cancer 39 2.363
279
P MJR001 Major Depressive Disorder 68 2.352
280
P OPT006 Optic Nerve Disease 57 2.352
281
c PRS130 Prostate Cancer, Hereditary, 8 32 2.350
282
c PRS136 Prostate Cancer, Hereditary, 6 33 2.350
283
BCT022 Bacterial Infectious Disease 55 2.347
284
P BCL017 B-Cell Lymphoma 57 2.334
285
ART016 Aortic Aneurysm 68 2.332
286
CHG001 Chagas Disease 65 2.331
287
ATX019 Ataxia with Vitamin E Deficiency 44 2.320
288
CRV035 Cervical Cancer 72 2.306
289
ATM095 Autoimmune Disease 61 2.297
290
c JVN010 Juvenile Rheumatoid Arthritis 52 2.275
291
INT078 Intracranial Thrombosis 50 2.255
292
P DRR001 Diarrhea 55 2.252
293
INT010 Intracranial Embolism 48 2.243
294
BLD053 Blood Platelet Disease 51 2.241
295
P THR005 Thrombotic Thrombocytopenic Purpura 64 2.237
296
P CRD119 Cardiac Arrest 68 2.226
297
CHL065 Cholangiocarcinoma 57 2.225
298
INT079 Intrahepatic Cholangiocarcinoma 51 2.225
299
HMN044 Human Immunodeficiency Virus Type 1 76 2.222
300
P HYP750 Hypertriglyceridemia, Familial 61 2.218
301
P NSP012 Nasopharyngeal Carcinoma 60 2.214
302
ULC004 Ulcerative Colitis 74 2.198
303
OST159 Osteogenic Sarcoma 66 2.198
304
c ACT027 Acute Pancreatitis 60 2.194
305
BWN001 Bowen-Conradi Syndrome 54 2.188
306
P HRP006 Herpes Simplex 65 2.186
307
SKN019 Skin Melanoma 70 2.186
308
c MCR112 Microvascular Complications of Diabetes 2 42 2.181
309
P EYD002 Eye Disease 57 2.181
310
AND005 Androgen Insensitivity Syndrome, Mild 21 2.179
311
P MCR129 Microvascular Complications of Diabetes 1 67 2.175
312
HMC014 Homocysteinemia 52 2.170
313
HYP266 Hypoxia 56 2.169
314
HRP004 Herpes Zoster 60 2.159
315
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 2.157
316
GLM045 Glioma 62 2.150
317
GLL048 Glial Tumor 51 2.150
318
BNR002 Bone Resorption Disease 47 2.146
319
HRT011 Heart Septal Defect 49 2.143
320
ALV005 Alveolar Soft Part Sarcoma 61 2.143
321
c ART101 Aortic Valve Disease 2 65 2.137
322
HLL004 Hellp Syndrome 53 2.133
323
IRN002 Iron Metabolism Disease 56 2.124
324
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 2.116
325
DRG024 Drug Allergy 40 2.107
326
P MYM013 Moyamoya Disease 1 59 2.105
327
P GLM007 Glomerulonephritis 59 2.103
328
CRD132 Cardiac Conduction Defect 59 2.094
329
ALC007 Alcohol Dependence 65 2.090
330
c SYS043 Systemic Lupus Erythematosus 1 38 2.087
331
P RTN014 Retinal Artery Occlusion 46 2.085
332
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 2.062
333
P INF037 Inflammatory Bowel Disease 53 2.054
334
c GLL024 Gallbladder Disease 1 53 2.051
335
PLM010 Pulmonary Edema 54 2.050
336
MLD018 Mild Cognitive Impairment 48 2.050
337
P LNG064 Lung Cancer Susceptibility 3 69 2.047
338
P ATR010 Atrial Heart Septal Defect 58 2.046
339
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 2.043
340
DYS073 Dysphagia 53 2.018
341
SPN035 Spindle Cell Sarcoma 51 2.014
342
SRC014 Sarcoma 64 2.014
343
IMM167 Immune Deficiency Disease 76 2.011
344
OVR029 Ovarian Hyperstimulation Syndrome 63 2.009
345
FDL002 Food Allergy 47 2.006
346
P MJR007 Major Affective Disorder 1 42 2.001
348
ING001 Inguinal Hernia 59 1.984
349
CHL068 Cholestasis 61 1.975
350
P INF038 Influenza 68 1.968
351
LNG099 Lung Disease 62 1.965
352
P NPH012 Nephrotic Syndrome 61 1.958
353
CMR002 Coumarin Resistance 59 1.952
354
GNG013 Gingivitis 59 1.950
355
MDD011 Mood Disorder 61 1.950
356
ECT026 Ectopic Pregnancy 47 1.947
357
IMP005 Impotence 52 1.942
358
PST053 Postherpetic Neuralgia 39 1.942
359
GST050 Gastrointestinal System Disease 55 1.940
360
c ATR087 Atrial Standstill 1 74 1.931
361
P EPL164 Epilepsy 70 1.913
362
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 1.898
363
GST009 Gastroschisis 53 1.897
364
CNN005 Connective Tissue Disease 66 1.892
365
c CHR711 Chronic Asthma 41 1.891
366
P LYM118 Lymphoma 66 1.889
367
SCK003 Sickle Cell Anemia 74 1.883
368
PNC041 Pancreatic Ductal Adenocarcinoma 51 1.880
369
BRN024 Bronchitis 67 1.865
370
IFP003 Ifap Syndrome 2 41 1.864
371
HMP001 Hemopericardium 47 1.863
372
c ACT071 Acute Kidney Failure 60 1.858
373
P PRC012 Pericardial Effusion 50 1.855
374
TBC004 Tobacco Addiction 63 1.853
375
P CHR345 Chronic Pain 50 1.853
376
P MGR001 Migraine Without Aura 48 1.839
377
VRC005 Varicose Veins 59 1.838
378
NRT001 Neurotic Disorder 56 1.835
379
RNL114 Renal Cell Carcinoma, Nonpapillary 79 1.834
380
SFT003 Soft Tissue Sarcoma 43 1.831
381
CLN045 Colonic Benign Neoplasm 48 1.831
382
VTM033 Vitamin K Deficiency Bleeding 49 1.821
383
c THR090 Thrombocythemia 1 50 1.820
384
P MGR003 Migraine with Aura 51 1.817
385
HMN014 Human Immunodeficiency Virus Infectious Disease 54 1.812
386
P VNS003 Venous Insufficiency 54 1.811
387
FCT001 Factor Viii Deficiency 61 1.796
388
P HYP086 Hypothyroidism 68 1.791
389
CRT004 Carotid Artery Thrombosis 39 1.790
390
GLS018 Glass Syndrome 60 1.788
391
MTR002 Mitral Valve Insufficiency 51 1.788
392
PPT002 Peptic Ulcer Perforation 34 1.786
393
P RNV001 Renovascular Hypertension 48 1.782
394
HPR003 Heparin-Induced Thrombocytopenia 47 1.780
395
RTN020 Retinal Vascular Disease 45 1.774
396
P HMP007 Hemophilia 52 1.758
397
FML035 Familial Hyperlipidemia 54 1.742
398
SPN051 Spondylitis 51 1.733
399
INF009 Inflammatory Spondylopathy 30 1.733
400
c SPN225 Spondyloarthropathy 1 70 1.729
401
HRD224 Hereditary Nonpolyposis Colon Cancer 51 1.727
402
NWB001 Newborn Respiratory Distress Syndrome 56 1.718
403
MNN020 Meningococcal Infection 44 1.717
404
NSS002 Neisseria Meningitidis Infection 46 1.717
405
LYM133 Lymphoma, Hodgkin, Classic 69 1.716
406
P HPT021 Hepatitis 68 1.716
407
P HYP076 Hyperthyroidism 53 1.710
408
ACQ007 Acquired Immunodeficiency Syndrome 58 1.707
409
PRT014 Protein S Deficiency 46 1.704
410
P THL005 Thalassemia 56 1.698
411
P HML002 Hemolytic Anemia 62 1.690
412
LFT001 Left Bundle Branch Hemiblock 47 1.686
413
P TBR001 Tuberous Sclerosis 69 1.685
414
P ALZ034 Alzheimer Disease 87 1.684
415
HRT012 Heart Valve Disease 53 1.677
416
P HMR003 Hemorrhagic Disease 59 1.666
417
DBT008 Diabetic Angiopathy 47 1.655
418
DRM006 Dermatitis 61 1.654
419
GST071 Gastrointestinal Carcinoma 46 1.652
420
GST049 Gastrointestinal System Cancer 49 1.652
421
CRT084 Creatinine Clearance Quantitative Trait Locus 25 1.650
422
GLC003 Glucose Intolerance 53 1.648
423
c HYP272 Hypercholesterolemia, Familial, 3 46 1.639
424
c LYS019 Loeys-Dietz Syndrome 1 57 1.639
425
c TBR026 Tuberous Sclerosis 2 71 1.632
426
NSP002 Nasopharyngitis 45 1.632
427
CHR001 Churg-Strauss Syndrome 61 1.630
428
ASP026 Asplenia, Isolated Congenital 43 1.629
429
MYC005 Myocardial Stunning 45 1.628
430
AMR003 Amaurosis Fugax 32 1.626
431
CNS004 Constipation 56 1.619
432
CRD223 Cardiac Arrhythmia 63 1.618
433
P GLM040 Glioma Susceptibility 1 70 1.617
434
BRN038 Bronchial Disease 51 1.604
435
CHL014 Cholera 62 1.600
436
P THY032 Thyroiditis 56 1.599
437
THR016 Thrombophlebitis 50 1.597
438
P NJM001 Nijmegen Breakage Syndrome 75 1.596
439
HDN002 Head Injury 44 1.588
440
c VRL010 Viral Hepatitis 52 1.587
441
SNG003 Single Ventricular Heart 30 1.585
442
P MYC008 Myocarditis 59 1.570
443
EPT021 Epithelial Recurrent Erosion Dystrophy 45 1.569
444
BRN026 Branch Retinal Artery Occlusion 41 1.567
445
CMP010 Complex Regional Pain Syndrome 59 1.562
446
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.560
447
AGG012 Aggressive Nk-Cell Leukemia 47 1.550
448
CRT015 Carotid Artery Occlusion 45 1.549
449
P NRB001 Neuroblastoma 66 1.547
450
THR035 Thrombasthenia 48 1.546
451
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 1.546
452
P CYS018 Cystitis 58 1.546
453
P SNS001 Sensorineural Hearing Loss 60 1.545
454
INT075 Intracranial Hypertension 52 1.545
455
WBR001 Weber Syndrome 38 1.534
456
SYS003 Systolic Heart Failure 49 1.530
457
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.524
458
P OST002 Osteoporosis 76 1.524
459
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 1.524
460
P LKM062 Leukemia, Acute Lymphoblastic 69 1.516
461
HYP060 Hyperinsulinism 53 1.511
462
CRB008 Cerebral Atherosclerosis 45 1.510
463
CYS001 Cystic Fibrosis 77 1.510
464
P HYD006 Hydrocephalus 62 1.506
465
RLP002 Relapsing-Remitting Multiple Sclerosis 56 1.504
466
STT002 Status Asthmaticus 49 1.500
467
c GRV008 Graves Disease 1 54 1.489
468
P LKM071 Leukemia, Chronic Lymphocytic 74 1.488
469
GST040 Gastric Adenocarcinoma 66 1.469
470
LCH001 Leech Infestation 37 1.469
471
TND005 Tendinitis 53 1.466
472
AGR002 Agoraphobia 45 1.458
473
MTB004 Metabolic Acidosis 48 1.450
474
PRC051 Paracetamol Poisoning 29 1.449
475
BNM001 Bone Marrow Cancer 45 1.444
476
c PRM012 Primary Polycythemia 58 1.439
477
PSY004 Psychotic Disorder 66 1.435
478
P AGG001 Aggressive Periodontitis 55 1.435
479
WTH001 Withdrawal Disorder 47 1.434
480
c MJR008 Major Affective Disorder 2 34 1.429
481
c MJR006 Major Affective Disorder 5 32 1.429
482
c MJR023 Major Affective Disorder 7 33 1.429
483
AMD002 Amed Syndrome, Digenic 36 1.429
484
c MJR004 Major Affective Disorder 4 28 1.429
485
c MJR003 Major Affective Disorder 6 32 1.429
486
EXP004 Exophthalmos 50 1.427
487
RTN003 Retinal Ischemia 48 1.423
488
NRM004 Neuroma 49 1.423
489
P MTR003 Mitral Valve Stenosis 53 1.419
490
c PRG042 Progressive Familial Heart Block, Type Ia 65 1.419
491
PSR001 Psoriatic Arthritis 61 1.418
492
KRT006 Keratoconjunctivitis 53 1.413
493
c HPT016 Hepatitis B 62 1.409
494
ACT011 Acute Contagious Conjunctivitis 41 1.408
495
RSP019 Respiratory Distress Syndrome in Premature Infants 52 1.402
496
DSS008 Disease of Mental Health 74 1.402
497
P FBR017 Fibrosarcoma 55 1.400
498
VRN004 Vernal Keratoconjunctivitis 47 1.397
499
c HPT001 Hepatitis C 61 1.397
500
LYM143 Lymphoma, Non-Hodgkin, Familial 74 1.385
501
ABD010 Abdominal Wall Defect 37 1.378
502
STM007 Stomatitis 52 1.372
503
P SLP006 Sleep Apnea 69 1.372
504
CNT028 Central Retinal Artery Occlusion 42 1.370
505
EXR010 Exercise-Induced Bronchoconstriction 34 1.362
506
ANG066 Angel-Shaped Phalangoepiphyseal Dysplasia 30 1.360
507
RTN021 Retinal Vascular Occlusion 45 1.352
508
P URN019 Urinary Tract Infection 48 1.348
509
BDD001 Budd-Chiari Syndrome 62 1.348
510
SPN186 Spinal Cord Injury 60 1.346
511
P PLY011 Polycystic Ovary Syndrome 57 1.339
512
SPP011 Suppression of Tumorigenicity 12 61 1.338
513
PLS009 Plasma Cell Neoplasm 64 1.338
514
LNG031 Lung Benign Neoplasm 51 1.338
515
c THR082 Thrombophilia Due to Activated Protein C Resistance 58 1.333
516
BLR013 Biliary Tract Cancer 43 1.331
517
c BSL007 Basal Cell Carcinoma 67 1.328
518
PLR008 Pleurisy 49 1.328
519
FRZ001 Frozen Shoulder 54 1.328
520
BRS064 Bursitis 51 1.328
521
c PCH010 Pachyonychia Congenita 3 43 1.325
522
NNL006 Non-Alcoholic Steatohepatitis 54 1.324
523
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 49 1.323
524
SCH003 Schizophreniform Disorder 54 1.323
525
CHR682 Chronic Bilirubin Encephalopathy 37 1.323
526
RSP007 Respiratory Distress Syndrome, Infant 41 1.323
527
ACT094 Acute Articular Rheumatism 24 1.320
528
PRT037 Pertussis 49 1.318
529
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 1.317
530
CLR109 Colorectal Adenocarcinoma 50 1.316
531
HYP056 Hypoglycemia 65 1.313
532
TND004 Tendinopathy 45 1.310
533
ISC015 Ischemic Colitis 43 1.310
534
RTN017 Retinal Detachment 60 1.307
535
HMT008 Hematuria, Benign Familial 54 1.306
536
SYN036 Syncope 44 1.298
537
PNC129 Pancreatic Adenocarcinoma 64 1.295
538
PRT011 Protein C Deficiency 47 1.294
539
DNT012 Dental Caries 53 1.293
540
P HYP061 Hypertrophic Cardiomyopathy 68 1.290
541
P PRS038 Personality Disorder 65 1.287
542
c SCN036 Secondary Progressive Multiple Sclerosis 55 1.279
543
P PTN014 Patent Ductus Arteriosus 1 59 1.279
544
P NRF002 Neurofibromatosis 60 1.278
545
NRR001 Neuroretinitis 42 1.277
546
RTN023 Retinitis 45 1.277
547
c HMP029 Hemophilia a 69 1.277
548
MDS022 Mediastinitis 47 1.277
549
c HPT073 Hepatitis C Virus 70 1.273
550
SPL018 Splenomegaly 47 1.272
551
P KHL003 Kohlschutter-Tonz Syndrome 57 1.271
552
GST045 Gastroenteritis 58 1.265
553
P MLG074 Malignant Mesenchymoma 40 1.264
554
CHR431 Chronic Venous Insufficiency 48 1.253
555
STT001 Status Epilepticus 58 1.253
556
c FML347 Familial Adenomatous Polyposis 2 56 1.251
557
MMM006 Mammographic Density 39 1.246
558
P PRK057 Parkinson Disease, Late-Onset 79 1.245
559
P SYS005 Systemic Scleroderma 73 1.245
560
END040 Endogenous Depression 54 1.244
561
PLC002 Plica Syndrome 35 1.232
562
GST013 Gastrojejunal Ulcer 41 1.231
563
P LKM002 Leukemia 65 1.227
564
SYN007 Synovitis 54 1.225
565
ART074 Aortic Dissection 53 1.223
566
P PNC025 Panic Disorder 52 1.220
567
GRN017 Granulocytopenia 42 1.216
568
PST011 Pustulosis of Palm and Sole 52 1.211
569
P MYP004 Myopathy 67 1.210
570
P ATR005 Atrophic Gastritis 50 1.210
571
OST003 Osteonecrosis 60 1.204
572
CRN019 Coronary Artery Vasospasm 47 1.204
573
c MYC058 Myocardial Infarction 2 23 1.202
574
TYP007 Typhoid Fever 63 1.201
575
MDD003 Middle Cerebral Artery Infarction 37 1.201
576
BRN028 Brain Cancer 73 1.200
577
ACT098 Acute Erythroid Leukemia 55 1.199
578
CRN020 Coronary Restenosis 39 1.197
579
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 1.192
580
P PSR002 Psoriasis 63 1.191
581
c SBC007 Subacute Thyroiditis 43 1.188
582
P GLL018 Gallbladder Cancer 59 1.187
583
IRN001 Iron Deficiency Anemia 58 1.186
584
ESP027 Esophagus Squamous Cell Carcinoma 45 1.185
585
ENT001 Enterocele 42 1.185
586
HNT002 Hantavirus Pulmonary Syndrome 55 1.185
587
FCT002 Factor Xi Deficiency 61 1.177
588
SBC016 Subacute Delirium 42 1.173
589
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.171
590
c DLT002 Dilated Cardiomyopathy 79 1.167
591
ANG049 Angioedema Induced by Ace Inhibitors 38 1.165
592
AYM001 Ayme-Gripp Syndrome 57 1.165
593
INT074 Intracranial Arteriosclerosis 23 1.165
594
c TBR025 Tuberous Sclerosis 1 84 1.165
595
P OPN001 Open-Angle Glaucoma 55 1.162
596
DFF005 Diffuse Large B-Cell Lymphoma 55 1.159
597
P BRN022 Bronchiectasis 59 1.154
598
c AMY091 Amyotrophic Lateral Sclerosis 1 87 1.153
599
P LTR001 Lateral Sclerosis 57 1.153
600
BTT017 Beta-Thalassemia Major 54 1.152
601
ANX010 Anxiety 70 1.148
602
P ENC018 Encephalopathy 62 1.146
603
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 1.145
604
CHR073 Choreatic Disease 53 1.145
605
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 33 1.140
606
INT323 Intraocular Pressure Quantitative Trait Locus 63 1.140
607
P HYP838 Hyperlipidemia, Familial Combined, 3 61 1.139
608
DDN004 Duodenogastric Reflux 31 1.136
609
THR123 Thrombotic Microangiopathy 40 1.136
610
c LKM061 Leukemia, Acute Myeloid 83 1.133
611
THR100 Thrombocytopenic Purpura, Autoimmune 60 1.128
612
HYP781 Hypoascorbemia 52 1.121
613
P CHL066 Cholangitis 51 1.119
614
ERY029 Erythermalgia, Primary 57 1.116
615
NRL016 Neural Tube Defects 80 1.111
616
PST021 Postpartum Depression 50 1.108
617
P EST001 Estrogen-Receptor Positive Breast Cancer 49 1.108
618
NRF028 Near-Fatal Asthma 27 1.108
619
SVR004 Severe Combined Immunodeficiency 70 1.108
620
ADN027 Adenomyosis 59 1.107
621
IMM102 Immunodeficiency 14 51 1.107
622
HYP458 Hyper Ige Syndrome 60 1.107
623
BLD051 Blood Coagulation Disease 52 1.107
624
c SCL052 Scleroderma, Familial Progressive 60 1.105
625
URM002 Uremia 47 1.104
626
MMB001 Membranoproliferative Glomerulonephritis 56 1.097
627
P BND020 Bone Disease 60 1.096
628
c ACT073 Acute Leukemia 59 1.090
629
KHN001 Kuhnt-Junius Degeneration 48 1.089
630
ALL014 Allergic Encephalomyelitis 34 1.089
631
ALL012 Allergic Angiitis 24 1.089
632
HYP005 Hypokalemia 55 1.081
633
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 1.081
634
CHL123 Chlamydia 58 1.081
635
BRN004 Brain Edema 54 1.073
636
P VNT002 Ventricular Septal Defect 58 1.066
637
ANG065 Angioma, Tufted 36 1.065
638
BRR002 Barrett's Adenocarcinoma 37 1.065
639
P HMR005 Hemorrhoid 49 1.065
640
TLN003 Telangiectasis 51 1.056
641
NPH009 Nephrolithiasis 54 1.055
642
P RNL015 Renal Hypertension 45 1.054
643
P MST009 Mastocytosis 64 1.054
644
CRD001 Cardiac Tamponade 44 1.053
645
OST160 Osteoid Osteoma 37 1.050
646
P MMB011 Membranous Nephropathy 50 1.048
647
RYN005 Raynaud Phenomenon 45 1.047
648
P TMP003 Temporal Arteritis 68 1.045
649
MNN043 Meningioma, Familial 79 1.041
650
HRW001 Hair Whorl 35 1.041
651
LYM002 Lymphoplasmacyte-Rich Meningioma 35 1.041
652
SCR001 Secretory Meningioma 40 1.041
653
INT395 Intracranial Meningioma 47 1.041
654
ADP007 Adie Pupil 40 1.037
655
HNM002 Hinman Syndrome 29 1.037
656
MST020 Mast Cell Activation Syndrome 27 1.036
657
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 1.034
658
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 1.034
659
BRG013 Buerger Disease 56 1.034
660
P ESN008 Eosinophilic Pneumonia 50 1.030
661
P ESP035 Esophagitis, Eosinophilic, 1 57 1.028
662
RNL065 Renal Cell Carcinoma, Papillary, 1 79 1.027
663
c PRM108 Primary Progressive Multiple Sclerosis 51 1.027
664
NRF026 Neurofibromatosis, Type Iv, of Riccardi 24 1.027
665
MCL069 Macular Dystrophy, Retinal, 1, North Carolina Type 38 1.027
666
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 59 1.027
667
c HYP839 Hyperlipidemia, Familial Combined, 1 30 1.027
668
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 52 1.027
669
MSC007 Muscle Hypertrophy 64 1.027
670
c OVR114 Ovarian Cancer 1 60 1.027
671
c AVS006 Avascular Necrosis of Femoral Head, Primary, 1 42 1.027
672
IMM240 Immunodeficiency 14a, Autosomal Dominant 52 1.027
673
c NRF023 Neurofibromatosis, Type Ii 70 1.027
674
P OCL013 Oculodentodigital Dysplasia 66 1.027
675
c HYP740 Hyperlipoproteinemia, Type V 54 1.027
676
SPR126 Superior Semicircular Canal Dehiscence 41 1.027
677
EXT006 Extrahepatic Cholestasis 41 1.027
678
RNL001 Renal Artery Obstruction 31 1.027
679
FLL027 Fallopian Tube Carcinoma 66 1.027
680
ADH001 Adhesions of Uterus 31 1.027
681
VSL002 Visual Epilepsy 39 1.027
682
NRF007 Neurofibroma 63 1.027
684
c HMG029 Hemoglobin Se Disease 41 1.027
685
HRT015 Heritable Pulmonary Arterial Hypertension 46 1.027
686
ASH001 Asherman's Syndrome 34 1.027
687
P HRD084 Hereditary Cerebral Amyloid Angiopathy 29 1.027
688
P TMP001 Temporal Lobe Epilepsy 49 1.021
689
CHL147 Chlamydia Pneumonia 47 1.021
690
INF118 Inflammatory Myopathy with Abundant Macrophages 27 1.021
691
CHR603 Chronic Enteropathy Associated with Slco2a1 Gene 25 1.018
692
P LPR021 Leprosy 3 71 1.011
693
ART004 Aortic Atherosclerosis 46 1.011
694
HNS001 Hansen's Disease 32 1.011
695
MTC151 Mitochondrial Complex I Deficiency, Nuclear Type 20 37 1.011
696
OPT010 Optic Papillitis 38 1.010
697
MCL006 Macular Retinal Edema 56 1.007
698
PLT015 Platelet Aggregation, Spontaneous 34 1.006
699
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 1.002
700
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 1.002
701
P CND004 Candidiasis 57 1.002
702
LMY002 Leiomyoma 51 1.002
703
GST037 Gastroparesis 52 1.000
704
CHL067 Cholecystitis 59 1.000
705
P CLL015 Collagen Disease 47 0.995
706
P SPP010 Suppressor of Tumorigenicity 3 50 0.992
707
CLF027 Cleft Palate, Isolated 64 0.992
708
c INH020 Inherited Metabolic Disorder 47 0.992
709
BNN003 Bone Inflammation Disease 47 0.991
710
CNT016 Central Retinal Vein Occlusion 53 0.987
711
PRT058 Pure Autonomic Failure 58 0.986
712
P PRK039 Parkinsonism 55 0.984
713
PLM001 Pulmonary Tuberculosis 69 0.984
714
HMN016 Hemangioendothelioma 35 0.981
715
KPS002 Kaposiform Hemangioendothelioma 50 0.981
716
SYS004 Systemic Mastocytosis 62 0.978
717
P HML001 Hemolytic-Uremic Syndrome 52 0.978
718
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 0.972
719
PLT031 Platelet Membrane Fluidity 28 0.970
720
CRB037 Cerebral Palsy 66 0.970
721
HGH043 High Grade Glioma 46 0.963
722
CHL004 Cholelithiasis 48 0.963
723
c FML346 Familial Adenomatous Polyposis 1 65 0.959
724
VRN001 Vernal Conjunctivitis 35 0.959
725
THY029 Thyroid Carcinoma 55 0.955
726
P MYP006 Myopia 55 0.948
727
BLL003 Bell's Palsy 48 0.943
728
INT067 Interstitial Nephritis 46 0.939
729
P UVT001 Uveitis 57 0.939
730
P ART005 Arteriovenous Malformation 64 0.938
731
ART008 Arteriosclerosis Obliterans 40 0.933
732
APN008 Apnea, Obstructive Sleep 66 0.932
733
NTR005 Nutritional Deficiency Disease 60 0.932
734
CHR100 Chronic Ulcer of Skin 57 0.931
735
HYP749 Hyperthermia, Cutaneous, with Headaches and Nausea 9 0.924
736
HMS001 Hemosiderosis 48 0.922
737
APC006 Apc-Associated Polyposis Conditions 22 0.922
738
P INS002 in Situ Carcinoma 52 0.922
739
ORL011 Oral Cancer 60 0.922
740
PRS045 Prostatic Hypertrophy 53 0.915
741
HMR002 Hemarthrosis 43 0.913
742
HSH003 Hashimoto Thyroiditis 60 0.912
743
CLF001 Cleft Lip 54 0.909
744
c ATM022 Autoimmune Myocarditis 35 0.904
745
P SYP003 Syphilis 59 0.904
746
ACT003 Acute Kidney Tubular Necrosis 46 0.904
747
LKP003 Leukoplakia 39 0.904
748
ARG002 Argininosuccinic Aciduria 61 0.898
749
P CRN035 Cranial Nerve Palsy 42 0.895
750
BNS003 Binswanger's Disease 41 0.895
751
ATX049 Ataxia with Vitamin 3 Deficiency 52 0.890
752
PRS021 Prostatic Adenoma 43 0.890
753
PPL022 Papilloma 53 0.886
754
P BNG032 Benign Mesothelioma 53 0.886
755
AMN001 Amenorrhea 53 0.886
756
ORP003 Oropharynx Cancer 54 0.886
757
P AMY004 Amyloidosis 69 0.886
758
EST002 Estrogen-Receptor Negative Breast Cancer 45 0.879
759
c ACQ017 Acquired Von Willebrand Syndrome 48 0.877
760
P MTR012 Mitral Valve Disease 57 0.877
761
CRT008 Carotid Artery Dissection 29 0.877
762
RNL077 Renal Fibrosis 46 0.876
763
GNG003 Gingival Recession 50 0.876
764
PRP016 Paraplegia 52 0.876
765
PRS129 Prostatic Hyperplasia, Benign 48 0.871
766
ESP002 Esophageal Varix 51 0.871
767
DVR002 Diverticulitis 46 0.871
768
HMG005 Hemoglobinopathy 55 0.866
769
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.864
770
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.857
771
PLS011 Plasmacytoma 56 0.856
772
ZLL002 Zollinger-Ellison Syndrome 55 0.855
774
ORL012 Oral Leukoplakia 35 0.853
775
THR017 Thoracoabdominal Syndrome 40 0.852
776
SYS071 Systemic Autoimmune Disease 35 0.850
777
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.845
778
MLG141 Malignant Atrophic Papulosis 35 0.845
779
ILS001 Ileus 49 0.845
780
CRB132 Cerebral Sinovenous Thrombosis 31 0.835
781
P FLL037 Follicular Lymphoma 66 0.834
782
NRN004 Neuroendocrine Tumor 55 0.834
783
IGG001 Iga Glomerulonephritis 50 0.834
784
P PLM036 Pulmonary Fibrosis 65 0.834
785
P PRN023 Prion Disease 60 0.834
786
INT276 Interatrial Communication 52 0.832
787
DNG003 Dengue Disease 65 0.830
788
P BRN019 Bernard-Soulier Syndrome 61 0.825
789
MYT019 May-Thurner Syndrome 27 0.824
790
MMM001 Mammary Paget's Disease 53 0.822
791
NCR002 Necrobiosis Lipoidica 38 0.822
792
c MST023 Mesothelioma, Malignant 56 0.822
793
TRN018 Transitional Cell Carcinoma 56 0.822
794
DBT007 Diabetic Cataract 36 0.822
795
CHR074 Choriocarcinoma 46 0.822
796
GST029 Gastric Cardia Adenocarcinoma 30 0.822
797
CNN003 Conn's Syndrome 77 0.821
798
CLL021 Collagenous Colitis 41 0.814
799
STR089 Storage Pool Platelet Disease 46 0.810
800
KRT019 Keratitis, Hereditary 66 0.810
801
P TTR001 Tetralogy of Fallot 69 0.810
802
IRD001 Iridocyclitis 54 0.810
803
P ALP008 Alopecia 53 0.810
804
OLG003 Oligohydramnios 50 0.807
805
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 54 0.804
806
P TRM003 Tremor 50 0.799
807
RDC002 Radiculopathy 51 0.797
808
c HRD002 Hereditary Angioedema 61 0.797
809
P MYT002 Myotonic Dystrophy 51 0.797
810
APP008 Appendicitis 62 0.797
811
P SML001 Small Cell Carcinoma 52 0.793
812
P END044 Endometriosis 62 0.791
813
RSP027 Respiratory Papillomatosis, Juvenile Recurrent, Congenital 47 0.785
814
ALN001 Aland Island Eye Disease 55 0.785
815
LNG105 Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome 36 0.785
816
SLT014 Salt and Pepper Developmental Regression Syndrome 43 0.785
817
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.785
818
P CNR004 Cone-Rod Dystrophy 2 74 0.785
819
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 57 0.785
820
ACT017 Acute Chest Syndrome 50 0.785
821
P CRV039 Cervicitis 52 0.785
822
DDN009 Duodenal Obstruction 34 0.785
823
P RTN018 Retinal Disease 53 0.785
824
ATM021 Autoimmune Inner Ear Disease 36 0.785
825
FCT007 Factor Vii Deficiency 64 0.784
826
HYP063 Hypersplenism 51 0.784
827
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 0.783
828
LVD003 Livedoid Vasculitis 37 0.783
829
NWC001 Newcastle Disease 47 0.783
830
CLL014 Cll/sll 45 0.783
831
MSC026 Muscular Dystrophy White Matter Spongiosis 13 0.783
832
ART109 Arterial Thoracic Outlet Syndrome 24 0.777
833
SKN016 Skin Disease 63 0.775
834
P INT068 Intestinal Disease 53 0.774
835
ART035 Arterial Calcification of Infancy 58 0.772
836
P CLC063 Celiac Disease 1 65 0.769
837
STC016 Sticky Platelet Syndrome 24 0.769
838
c ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.769
839
OTT002 Otitis Media 70 0.767
840
HMN047 Human Cytomegalovirus Infection 59 0.759
841
TRC022 Tricuspid Valve Insufficiency 46 0.758
842
ANT009 Antithrombin Iii Deficiency 59 0.756
843
P GRV001 Graves' Disease 54 0.756
844
HYP540 Hypertension, Diastolic 38 0.753
845
MGS001 Megaesophagus 44 0.753
846
PYL006 Pyloric Stenosis 48 0.753
847
SNL007 Senile Cataract 40 0.753
848
HRN026 Hernia, Hiatus 46 0.750
849
P ERY036 Erythema Nodosum 49 0.750
850
DBT010 Diabetic Neuropathy 54 0.750
851
P PTS002 Ptosis 52 0.741
852
MSL001 Measles 61 0.741
853
P HYP055 Hypoplastic Left Heart Syndrome 65 0.741
854
CNT060 Central Serous Chorioretinopathy 38 0.741
855
ATR024 Atrial Fibrillation and Stroke 22 0.740
856
TTH007 Tooth Erosion 30 0.736
857
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.733
858
LWC002 Lowe Oculocerebrorenal Syndrome 68 0.733
859
PYR004 Pyuria 36 0.731
860
SLN001 Silent Myocardial Infarction 33 0.731
861
P RRH023 Rare Hereditary Hemochromatosis 52 0.731
862
PRD004 Prediabetes Syndrome 52 0.726
863
P NRV007 Nervous System Disease 65 0.726
864
c PRM038 Primary Agammaglobulinemia 47 0.726
865
MCR191 Microscopic Colitis 46 0.722
866
PNC085 Penicillin Allergy 43 0.722
867
BLR008 Bilirubin Metabolic Disorder 57 0.722
868
P HRN001 Horner's Syndrome 45 0.722
869
c FML021 Familial Hypercholesterolemia 71 0.722
870
RTN004 Retinal Microaneurysm 32 0.718
871
TRC005 Tracheal Stenosis 43 0.718
872
P HRD008 Hereditary Hemorrhagic Telangiectasia 64 0.718
873
THY030 Thyroid Gland Disease 50 0.713
874
P PHC003 Pheochromocytoma 70 0.712
875
c ACT134 Acute Liver Failure 57 0.712
876
RST023 Resting Heart Rate, Variation in 40 0.702
877
ADR040 Adrenal Gland Pheochromocytoma 45 0.702
878
HPT019 Hepatic Encephalopathy 59 0.702
879
BLR002 Bile Reflux 38 0.702
880
HPT004 Hepatic Coma 43 0.702
881
ANX004 Anoxia 40 0.702
882
PRS063 Paresthesia 39 0.702
883
c ATM104 Autoimmune Vasculitis 37 0.696
884
P RSS029 Resistance to Thyroid Hormone Due to a Mutation in Thyroid Hormone Receptor Alpha 16 0.696
885
SND002 Sneddon Syndrome 48 0.696
886
MNS015 Monosodium Glutamate Sensitivity 18 0.696
887
ATY005 Atypical Teratoid Rhabdoid Tumor 69 0.695
888
MTC027 Mitochondrial Trifunctional Protein Deficiency 58 0.692
889
LNG073 Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 58 0.692
890
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 58 0.692
891
ACY005 Acyl-Coa Dehydrogenase, Short-Chain, Deficiency of 54 0.692
892
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 63 0.692
893
CRN295 Carnitine Palmitoyltransferase I Deficiency 55 0.692
894
3HY007 3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency 51 0.692
895
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.692
896
3MT001 3-Methylcrotonyl-Coa Carboxylase Deficiency 52 0.692
897
CRN239 Carnitine Deficiency, Systemic Primary 62 0.692
898
CHK001 Chikungunya 60 0.692
899
T2H001 T2-High Asthma 9 0.692
900
AQG004 Aquagenic Syringeal Acrokeratoderma 17 0.692
901
c BTT014 Beta-Thalassemia 72 0.692
902
SPN369 Spinal Disease 43 0.692
903
PRC003 Proctitis 49 0.692
904
ANL017 Anal Squamous Cell Carcinoma 44 0.692
905
FML037 Female Breast Cancer 51 0.681
906
P ANP001 Anaplastic Large Cell Lymphoma 59 0.681
907
DMY004 Demyelinating Disease 50 0.681
908
BRS051 Breast Disease 58 0.681
909
PST092 Posttransplant Acute Limbic Encephalitis 29 0.681
910
RDT013 Radiation Proctitis 47 0.681
911
SPN185 Spinal Cord Infarction 28 0.677
912
INS024 Insulin-Like Growth Factor I 77 0.670
913
LPT014 Leptin Deficiency or Dysfunction 77 0.670
914
VCC001 Vaccinia 49 0.670
915
P HRM001 Hermansky-Pudlak Syndrome 65 0.670
916
CHR178 Chromosomal Triplication 33 0.670
917
CTS005 Catastrophic Antiphospholipid Syndrome 43 0.659
918
P OMP004 Omphalocele 47 0.658
920
c JVN061 Juvenile Arthritis 56 0.658
921
P ATX030 Ataxia-Telangiectasia 80 0.658
922
ANV001 Anovulation 46 0.658
923
P BRS044 Breast Adenocarcinoma 58 0.658
924
CHL035 Cholinergic Urticaria 29 0.658
925
DGN001 Degenerative Disc Disease 48 0.658
926
ERY069 Erythrokeratoderma ''en Cocardes'' 26 0.658
927
PRN011 Pernicious Anemia 52 0.656
928
SPT005 Spotted Fever 49 0.656
929
SDD008 Sudden Sensorineural Hearing Loss 41 0.656
930
C1N001 C1 Inhibitor Deficiency 43 0.647
931
CNN010 Connective Tissue Benign Neoplasm 44 0.647
932
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 65 0.647
933
APR006 Apert Syndrome 69 0.647
934
c CRN243 Carney Complex, Type 1 53 0.647
935
P MLN066 Melanoma, Cutaneous Malignant 1 65 0.647
936
AND020 Androgen Insensitivity, Partial 54 0.647
937
VSL013 Visual Impairment and Progressive Phthisis Bulbi 36 0.647
938
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.647
939
CLF044 Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly 30 0.647
940
ALP103 Alpha-1-Antitrypsin Deficiency 67 0.647
941
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 38 0.647
942
P OCY003 Oocyte Maturation Defect 1 46 0.647
943
HYP555 Hypertriglyceridemia, Transient Infantile 39 0.647
944
SKN013 Skin Benign Neoplasm 49 0.647
945
FST001 Foster-Kennedy Syndrome 39 0.647
946
HYP081 Hypolipoproteinemia 49 0.647
947
P PLM034 Pulmonary Emphysema 58 0.647
948
CYT004 Cytomegalic Inclusion Disease 31 0.647
949
49X006 49, Xxxxy Syndrome 40 0.647
950
UND007 Undifferentiated Connective Tissue Disease 29 0.647
951
IMM003 Immunoglobulin Alpha Deficiency 44 0.646
952
ORL015 Oral Squamous Cell Carcinoma 43 0.646
953
HYP017 Hypophosphatemia 49 0.646
954
c CHL119 Cholangitis, Primary Sclerosing 57 0.646
956
GST019 Gastrointestinal Stromal Tumor