Search results for coronary artery disease, modifier of

660 hits were found for coronary artery disease, modifier of

# Family MCID Name MIFTS Score
1
P HYP607 Hypercholesterolemia, Familial 81 2.936
2
ART140 Arteries, Anomalies of 51 1.309
3
P CRN018 Coronary Artery Anomaly 69 1.292
4
P CRN300 Coronary Heart Disease 1 57 0.931
5
ISC004 Ischemia 66 0.867
6
P HRT032 Heart Disease 80 0.835
7
ISC006 Ischemic Heart Disease 73 0.765
8
P MYC007 Myocardial Infarction 81 0.733
9
ANR040 Aneurysm 61 0.726
10
P ART021 Arteriosclerosis 62 0.700
11
VSC007 Vascular Disease 71 0.692
12
END072 Endotheliitis 46 0.627
13
THR024 Thrombosis 61 0.601
14
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.495
15
CRB009 Cerebritis 41 0.480
16
c BLD140 Blood Group, I System 37 0.454
17
AGN016 Aging 65 0.443
18
P DBT009 Diabetes Mellitus 72 0.441
19
P CRN074 Coronary Artery Aneurysm 47 0.416
20
CRN030 Coronary Stenosis 52 0.407
21
ANG054 Angina Pectoris 53 0.401
22
c ACT075 Acute Myocardial Infarction 64 0.397
23
P HPT021 Hepatitis 75 0.393
24
P KDN018 Kidney Disease 69 0.373
25
RTN023 Retinitis 52 0.355
26
P ART022 Arthritis 77 0.343
27
P BRS047 Breast Cancer 100 0.321
28
KWS002 Kawasaki Disease 72 0.315
29
PRP080 Peripheral Artery Disease 54 0.308
30
LNG099 Lung Disease 67 0.305
31
TRN044 Transposition of the Great Arteries 49 0.301
32
P LKM002 Leukemia 75 0.300
33
P LYM118 Lymphoma 71 0.300
34
CRN017 Coronary Thrombosis 48 0.290
35
P ALZ034 Alzheimer Disease 95 0.289
36
CNG034 Congestive Heart Failure 74 0.289
37
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.284
38
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.284
39
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.283
40
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.283
41
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.283
42
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.283
43
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.283
44
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.283
45
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.283
46
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.283
47
P LVR013 Liver Disease 76 0.281
48
CRT016 Carotid Artery Disease 58 0.277
49
P ATR011 Atrial Fibrillation 68 0.276
50
P RHM011 Rheumatoid Arthritis 91 0.276
51
c PLM164 Pulmonary Hypertension, Primary, 1 67 0.274
52
RSP006 Respiratory System Disease 63 0.272
53
PRP027 Peripheral Vascular Disease 71 0.270
54
NRN002 Neuronitis 43 0.270
55
c CHR089 Chronic Kidney Failure 72 0.263
56
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.263
57
P CRV039 Cervicitis 49 0.262
58
URN009 Urinary System Disease 58 0.260
59
P ENC018 Encephalopathy 58 0.260
60
CRB039 Cerebrovascular Disease 68 0.258
61
P ADN016 Adenocarcinoma 71 0.256
62
P PNC044 Pancreatitis 64 0.255
63
P PLM037 Pulmonary Hypertension 79 0.254
64
AST005 Asthma 83 0.254
65
ERY003 Erythema Multiforme 60 0.254
66
CNN005 Connective Tissue Disease 65 0.251
67
P THY032 Thyroiditis 56 0.248
68
PRS047 Prostatitis 59 0.247
69
ATM095 Autoimmune Disease 66 0.245
70
P PNM007 Pneumonia 70 0.239
71
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.238
72
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.237
73
P NRP001 Neuropathy 63 0.237
74
HYP266 Hypoxia 61 0.236
75
P CLR023 Colorectal Cancer 98 0.230
76
c CNT035 Central Nervous System Disease 65 0.228
77
ANX010 Anxiety 72 0.226
78
IMM136 Immune System Disease 57 0.224
79
MNT002 Mental Depression 60 0.222
80
ART016 Aortic Aneurysm 70 0.221
81
RHM027 Rheumatic Disease 62 0.220
82
P LPS004 Lupus Erythematosus 69 0.219
83
c HYP805 Hypercholesterolemia, Autosomal Dominant, 3 47 0.218
84
P LNG032 Lung Cancer 99 0.217
85
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.216
86
GLC008 Glucose Metabolism Disease 38 0.215
87
SPS003 Spastic Diplegia 55 0.211
88
P NRV007 Nervous System Disease 75 0.210
89
P PRD008 Periodontitis 67 0.208
90
MLN008 Melanoma 72 0.208
91
c SYS001 Systemic Lupus Erythematosus 86 0.208
92
CRB004 Cerebral Artery Occlusion 46 0.206
93
ACQ007 Acquired Immunodeficiency Syndrome 65 0.203
94
P VNT002 Ventricular Septal Defect 59 0.201
95
STR067 Stroke, Ischemic 84 0.201
96
GST050 Gastrointestinal System Disease 66 0.199
97
P CLL015 Collagen Disease 53 0.199
98
P PRS040 Prostate Cancer 88 0.196
99
P ART023 Arthropathy 68 0.195
100
DMN002 Dementia 68 0.194
101
P INT068 Intestinal Disease 65 0.192
102
LPD008 Lipid Metabolism Disorder 59 0.192
103
INT007 Intermediate Coronary Syndrome 55 0.191
104
ENT004 Enthesopathy 38 0.190
105
CRT015 Carotid Artery Occlusion 42 0.189
106
P MLT020 Multiple Sclerosis 85 0.187
107
JNT002 Joint Disorders 60 0.187
108
SKN016 Skin Disease 68 0.186
109
SRC014 Sarcoma 68 0.186
110
VRL011 Viral Infectious Disease 64 0.184
111
P SLP006 Sleep Apnea 65 0.180
112
P ESP024 Esophagitis 64 0.179
113
ADN018 Adenoma 63 0.177
114
DBL004 Double Discordia 19 0.175
115
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.175
116
P TTR001 Tetralogy of Fallot 70 0.174
117
LMB062 Limb Ischemia 52 0.174
118
HYP066 Hyperglycemia 64 0.172
119
GST053 Gastric Cancer 84 0.172
120
P INF038 Influenza 77 0.172
121
c HYP595 Hypertension, Essential 78 0.171
122
MDS022 Mediastinitis 44 0.170
123
SKN027 Skin Conditions 48 0.169
124
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.167
125
P MYC084 Mycobacterium Tuberculosis 1 69 0.166
126
SPS057 Spasticity 41 0.166
127
P MYP006 Myopia 56 0.165
128
P SCH015 Schizophrenia 71 0.165
129
VSC011 Vasculitis 66 0.164
130
HRT015 Heritable Pulmonary Arterial Hypertension 48 0.163
131
P EPL164 Epilepsy 70 0.162
132
OST012 Osteoarthritis 88 0.162
133
CRD119 Cardiac Arrest 63 0.161
134
APN008 Apnea, Obstructive Sleep 67 0.160
135
CNG134 Congenitally Corrected Transposition of the Great Arteries 28 0.160
136
DXT001 Dextrocardia 55 0.159
137
PSY004 Psychotic Disorder 72 0.158
138
P INF032 Infertility 59 0.158
139
END030 End Stage Renal Failure 59 0.157
140
c HPT001 Hepatitis C 73 0.156
141
SLP005 Sleep Disorder 59 0.156
142
CRT013 Carotid Stenosis 52 0.155
143
PRD007 Periodontal Disease 64 0.154
144
P OVR042 Ovarian Cancer 82 0.153
145
LYM024 Lymphatic System Disease 45 0.153
146
HDC001 Headache 55 0.152
147
P MYM013 Moyamoya Disease 1 50 0.152
148
INT002 Intermittent Claudication 61 0.152
149
c ART101 Aortic Valve Disease 2 65 0.151
150
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.151
151
P HYP086 Hypothyroidism 62 0.150
152
FTT001 Fatty Liver Disease 62 0.150
153
P END033 Endocarditis 58 0.150
154
CRT049 Critical Limb Ischemia 56 0.150
155
CHL123 Chlamydia 64 0.150
156
INF013 Inferior Myocardial Infarction 36 0.149
157
P THR014 Thrombocytopenia 65 0.146
158
P HYP055 Hypoplastic Left Heart Syndrome 63 0.146
159
P HYP061 Hypertrophic Cardiomyopathy 65 0.146
160
P PSR002 Psoriasis 65 0.145
161
CRH001 Crohn's Disease 80 0.144
162
c HYP543 Hypoplastic Left Heart Syndrome 1 38 0.144
163
c TRC078 Trichohepatoenteric Syndrome 2 34 0.144
164
BRN071 Brain Injury 54 0.143
165
P HMP007 Hemophilia 61 0.143
166
c THR092 Thrombophilia Due to Thrombin Defect 61 0.141
167
P INF037 Inflammatory Bowel Disease 52 0.140
168
P MYC008 Myocarditis 58 0.139
169
P MNN013 Meningitis 71 0.138
170
SPL005 Splenic Artery Aneurysm 32 0.138
171
P ART084 Arteriovenous Fistula 46 0.138
172
ART004 Aortic Atherosclerosis 48 0.138
173
PRT036 Peritonitis 67 0.136
174
CRD001 Cardiac Tamponade 45 0.136
175
LYM019 Lymphosarcoma 58 0.136
176
P BCL006 B-Cell Lymphomas 70 0.136
177
P ANT006 Antiphospholipid Syndrome 59 0.135
178
ART012 Aortitis 33 0.135
179
P PLY014 Polycystic Kidney Disease 60 0.135
180
HYP060 Hyperinsulinism 56 0.134
181
BRS051 Breast Disease 67 0.134
182
CLT003 Colitis 63 0.134
183
MRF001 Marfan Syndrome 75 0.133
184
BNF002 Bone Fracture 56 0.133
185
P RNG031 Ring Chromosome Y Syndrome 29 0.133
186
RCT017 Rectal Disease 38 0.133
187
BDY007 Body Mass Index Quantitative Trait Locus 1 23 0.132
188
P THL005 Thalassemia 65 0.132
189
RNL114 Renal Cell Carcinoma, Nonpapillary 68 0.131
190
P DLT002 Dilated Cardiomyopathy 76 0.131
191
STS002 Situs Inversus 48 0.131
192
PLM033 Pulmonary Embolism 62 0.131
193
c SCL052 Scleroderma, Familial Progressive 60 0.130
194
P RTN024 Retinoblastoma 76 0.130
195
c HPT016 Hepatitis B 68 0.130
196
DRM006 Dermatitis 67 0.129
197
P MYP004 Myopathy 69 0.129
198
P OST002 Osteoporosis 75 0.129
199
P AMY004 Amyloidosis 69 0.129
200
GLC003 Glucose Intolerance 58 0.128
201
BRN106 Burns 57 0.128
202
MDD011 Mood Disorder 64 0.128
203
c HPT073 Hepatitis C Virus 73 0.126
204
MTH009 Mouth Disease 64 0.126
205
CNT061 Conotruncal Heart Malformations 70 0.126
206
MYL069 Myeloma, Multiple 86 0.126
207
P ANR048 Aniridia 1 68 0.126
208
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 54 0.125
209
P HMR003 Hemorrhagic Disease 61 0.125
210
SPN051 Spondylitis 55 0.125
211
P TRC086 Trichohepatoenteric Syndrome 1 54 0.124
212
INS024 Insulin-Like Growth Factor I 83 0.124
213
PRC013 Pericarditis 55 0.122
214
c MLT151 Multiple Mitochondrial Dysfunctions Syndrome 5 36 0.122
215
GNG013 Gingivitis 64 0.122
216
DYS073 Dysphagia 47 0.122
217
NRM005 Neuromuscular Disease 60 0.122
218
BRC012 Brucellosis 71 0.122
219
P CRD132 Cardiac Conduction Defect 53 0.121
220
P PRK057 Parkinson Disease, Late-Onset 78 0.121
221
HMP001 Hemopericardium 34 0.120
222
INF009 Inflammatory Spondylopathy 32 0.120
223
P MTR012 Mitral Valve Disease 59 0.120
224
P CNJ013 Conjunctivitis 67 0.120
225
c HPT003 Hepatitis a 63 0.119
226
HMN044 Human Immunodeficiency Virus Type 1 71 0.119
227
HMT018 Hematopoietic Stem Cell Transplantation 58 0.119
228
P CTR002 Cataract 60 0.119
229
c SPN225 Spondyloarthropathy 1 71 0.119
230
PRP030 Purpura 61 0.119
231
VNW001 Von Willebrand's Disease 61 0.118
232
GT001 Gout 60 0.118
233
TRC062 Tricuspid Atresia 47 0.116
234
BRN080 Brain Ischemia 45 0.116
235
ART005 Arteriovenous Malformation 64 0.116
236
P ART034 Aortopulmonary Window 25 0.116
237
RTN018 Retinal Disease 56 0.115
238
c MTR002 Mitral Valve Insufficiency 46 0.115
239
PLY112 Polyarteritis Nodosa, Childhood-Onset 39 0.115
240
LYM133 Lymphoma, Hodgkin, Classic 78 0.115
241
P MCR115 Microvascular Complications of Diabetes 5 66 0.115
242
P PTN014 Patent Ductus Arteriosus 1 45 0.115
243
NRF026 Neurofibromatosis, Type Iv, of Riccardi 72 0.115
244
P BLD051 Blood Coagulation Disease 38 0.115
245
P RSP003 Respiratory Failure 71 0.115
246
P HYP076 Hyperthyroidism 56 0.115
247
P PLY011 Polycystic Ovary Syndrome 65 0.114
248
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.114
249
MYL009 Myelodysplastic Syndrome 75 0.114
250
SPR004 Supravalvular Aortic Stenosis 54 0.114
251
ART017 Aortic Disease 57 0.114
252
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 42 0.114
253
BRR014 Barrett Esophagus 64 0.113
254
PNG002 Pain Agnosia 41 0.113
255
GST045 Gastroenteritis 65 0.113
256
P MSC005 Muscular Dystrophy 66 0.113
257
PST011 Pustulosis of Palm and Sole 47 0.113
258
SCK005 Sickle Cell Disease 54 0.113
259
NRN004 Neuroendocrine Tumor 58 0.113
260
c HMP029 Hemophilia a 69 0.113
261
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.112
262
P CLC063 Celiac Disease 1 65 0.112
263
HYP056 Hypoglycemia 62 0.112
264
P EHL001 Ehlers-Danlos Syndrome 61 0.112
265
THR100 Thrombocytopenic Purpura, Autoimmune 57 0.111
266
ULC004 Ulcerative Colitis 80 0.111
267
P HRP006 Herpes Simplex 70 0.111
268
MGR028 Migraine with or Without Aura 1 55 0.111
269
TTH006 Tooth Disease 54 0.110
270
ANX004 Anoxia 49 0.110
271
P DRR001 Diarrhea 60 0.110
272
P INT030 Intracranial Aneurysm 58 0.110
273
c PRC016 Pre-Eclampsia 65 0.110
274
PRS042 Prostate Disease 56 0.110
275
P EXN002 Exanthem 62 0.110
276
P SNS014 Sinusitis 62 0.109
277
PLC008 Placenta Disease 48 0.109
278
P TMP003 Temporal Arteritis 67 0.109
279
P PLY017 Polyarteritis Nodosa 51 0.109
280
LVR012 Liver Cirrhosis 73 0.109
281
NRT004 Neuritis 55 0.109
282
PSR001 Psoriatic Arthritis 66 0.109
283
P ESS003 Essential Thrombocythemia 71 0.108
284
P GLM007 Glomerulonephritis 61 0.108
285
P STR035 Streptococcal Group a Invasive Disease 28 0.108
286
P PRC012 Pericardial Effusion 52 0.108
287
P THR015 Thrombophilia 58 0.107
288
P HYP069 Hyperparathyroidism 58 0.107
289
INF034 Infective Endocarditis 56 0.107
290
P RNV001 Renovascular Hypertension 48 0.107
291
c HMP004 Hemophilia B 67 0.106
292
SYN036 Syncope 46 0.106
293
P RTN022 Retinal Vein Occlusion 53 0.105
294
OST062 Osteoarthritis with Mild Chondrodysplasia 43 0.105
295
SCK003 Sickle Cell Anemia 73 0.105
296
P GRV001 Graves' Disease 62 0.105
297
c PNS012 Paine Syndrome 52 0.104
298
P ART067 Aortic Aneurysm, Familial Thoracic 1 65 0.104
299
PTN001 Patent Foramen Ovale 58 0.104
300
P PLY018 Polycythemia 60 0.103
301
ESP023 Esophageal Disease 58 0.102
302
c ACT027 Acute Pancreatitis 61 0.102
303
GTR002 Goiter 53 0.102
304
GST092 Gastroesophageal Reflux 64 0.101
305
SPN186 Spinal Cord Injury 67 0.100
306
MSC033 Muscle Disorders 53 0.100
307
P PHC003 Pheochromocytoma 72 0.100
308
RST023 Resting Heart Rate, Variation in 42 0.099
309
P HMN010 Hemangioma 61 0.099
310
PRP016 Paraplegia 53 0.099
311
P HYP750 Hypertriglyceridemia, Familial 55 0.099
312
c MNN043 Meningioma, Familial 69 0.099
313
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.099
314
BCK006 Back Pain 46 0.099
315
HLC007 Helicobacter Pylori Infection 64 0.098
316
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.098
317
P ALP008 Alopecia 56 0.098
318
P GLY013 Glycogen Storage Disease 61 0.098
319
CRT004 Carotid Artery Thrombosis 37 0.097
320
OVR063 Overnutrition 53 0.097
321
P HYP014 Hyperuricemia 54 0.097
322
P ORT004 Orthostatic Intolerance 68 0.096
323
LYM143 Lymphoma, Non-Hodgkin, Familial 71 0.096
324
MSC004 Muscle Tissue Disease 39 0.096
325
CHR001 Churg-Strauss Syndrome 51 0.095
326
BNM029 Bone Mineral Density Quantitative Trait Locus 15 39 0.095
327
PLY001 Polycythemia Vera 75 0.095
328
SPN041 Spinal Cord Disease 54 0.095
329
BNM022 Bone Mineral Density Quantitative Trait Locus 8 32 0.095
330
HPR003 Heparin-Induced Thrombocytopenia 48 0.095
331
URT001 Urethritis 44 0.094
332
NNL002 Nonalcoholic Steatohepatitis 56 0.094
333
CHL067 Cholecystitis 58 0.094
334
c MCL042 Macular Degeneration, Age-Related, 1 79 0.093
335
ATN004 Autonomic Neuropathy 46 0.093
336
TKY002 Takayasu Arteritis 66 0.093
337
TRN015 Transient Cerebral Ischemia 58 0.093
338
PHR003 Pharyngitis 59 0.093
339
c CTR119 Cataract 32, Multiple Types 32 0.093
340
P LNG028 Long Qt Syndrome 63 0.093
341
P MJR001 Major Depressive Disorder 70 0.093
342
SYN007 Synovitis 61 0.093
343
ACR007 Acromegaly 70 0.092
344
DSS009 Disseminated Intravascular Coagulation 56 0.092
345
BRN022 Bronchiectasis 55 0.092
346
WLL001 Williams-Beuren Syndrome 63 0.092
347
ESP021 Esophageal Cancer 79 0.092
348
BRN028 Brain Cancer 72 0.092
349
P HMR012 Hemorrhagic Fever 60 0.092
350
P ATR001 Atrioventricular Septal Defect 56 0.092
351
SPN369 Spinal Disease 42 0.092
352
CRD223 Cardiac Arrhythmia 52 0.092
353
PLM070 Pulmonic Stenosis 61 0.091
354
FBR012 Fabry Disease 72 0.091
355
P CHR345 Chronic Pain 52 0.091
356
STM006 Stomach Disease 52 0.091
357
ASP030 Aspirin Resistance 44 0.091
358
MYM001 Myoma 56 0.091
359
BRN038 Bronchial Disease 58 0.091
360
P NPH012 Nephrotic Syndrome 60 0.091
361
HMP005 Hemiplegia 54 0.091
362
URM002 Uremia 52 0.091
363
c HYP555 Hypertriglyceridemia, Transient Infantile 34 0.091
364
c MCR113 Microvascular Complications of Diabetes 3 55 0.091
365
P SYS005 Systemic Scleroderma 67 0.090
366
P HYP614 Hyperlipidemia, Familial Combined 57 0.090
367
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.090
368
CLP006 Clopidogrel Resistance 42 0.090
369
DFF005 Diffuse Large B-Cell Lymphoma 64 0.090
370
P GST044 Gastritis 61 0.090
371
P UVT001 Uveitis 61 0.089
372
WLF001 Wolff-Parkinson-White Syndrome 57 0.089
373
c BTT014 Beta-Thalassemia 70 0.089
374
VSC008 Vascular Hemostatic Disease 36 0.089
375
BRN002 Bronchiolitis 59 0.089
376
c CNT016 Central Retinal Vein Occlusion 50 0.088
377
P NTR004 Neutropenia 60 0.088
378
P PSD087 Pseudoxanthoma Elasticum 67 0.088
379
P DBT005 Diabetes Insipidus 54 0.088
380
HRP004 Herpes Zoster 61 0.088
381
HMZ003 Homozygous Familial Hypercholesterolemia 54 0.087
382
ALL026 Allergic Hypersensitivity Disease 59 0.087
383
BRT054 Brittle Bone Disorder 67 0.087
384
P PRP029 Porphyria 62 0.086
385
P TRN020 Turner Syndrome 69 0.086
386
PRP019 Peripheral Nervous System Disease 53 0.086
387
P OVR049 Ovarian Disease 58 0.086
388
P MYL005 Myelofibrosis 75 0.086
389
P VNS003 Venous Insufficiency 53 0.086
390
P PLY019 Polyneuropathy 58 0.086
391
ALP046 Alport Syndrome, X-Linked 74 0.085
392
P DRM010 Dermatomyositis 65 0.085
393
P MCP040 Mucopolysaccharidosis-Plus Syndrome 61 0.085
394
ATN005 Autonomic Dysfunction 51 0.085
395
ANG066 Angel-Shaped Phalangoepiphyseal Dysplasia 33 0.085
396
LYM017 Lyme Disease 68 0.084
397
GNG011 Gingival Disease 50 0.084
398
P CHR071 Charcot-Marie-Tooth Disease 67 0.084
399
c MCR130 Microvascular Complications of Diabetes 6 42 0.084
400
c MCR120 Microvascular Complications of Diabetes 7 34 0.084
401
c MCR133 Microvascular Complications of Diabetes 4 32 0.084
402
GST023 Gastric Ulcer 57 0.084
403
P DDN001 Duodenal Ulcer 53 0.083
404
P PTS002 Ptosis 50 0.083
405
CNS004 Constipation 57 0.083
406
P BPL003 Bipolar Disorder 61 0.083
407
SCH014 Schistosomiasis 62 0.082
408
ART008 Arteriosclerosis Obliterans 45 0.082
409
PLM001 Pulmonary Tuberculosis 72 0.082
410
P CHL066 Cholangitis 52 0.082
411
MNS002 Mini Stroke 23 0.082
412
P DBT085 Diabetes Mellitus, Insulin-Dependent 69 0.082
413
HYP025 Hyperphosphatemia 48 0.082
414
P RNL015 Renal Hypertension 46 0.082
415
GST033 Gestational Diabetes 62 0.082
416
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 36 0.081
417
P PLM036 Pulmonary Fibrosis 68 0.081
418
c BRN108 Branchiootic Syndrome 1 47 0.081
419
GRW007 Growth Hormone Deficiency 52 0.081
420
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 63 0.081
421
THY030 Thyroid Gland Disease 51 0.081
422
c ACT210 Acute Respiratory Distress Syndrome 63 0.081
423
PRD004 Prediabetes Syndrome 46 0.080
424
P VSC018 Visceral Steatosis 38 0.080
425
P CMP008 Compartment Syndrome 48 0.080
426
P BRG001 Brugada Syndrome 61 0.080
427
PRT018 Portal Vein Thrombosis 50 0.080
428
P PNC025 Panic Disorder 57 0.080
429
P ANG015 Angioedema 57 0.080
430
P TRC005 Tracheal Stenosis 39 0.080
431
CRD016 Cardiac Rupture 34 0.079
432
BRS090 Breast Reconstruction 41 0.079
433
DWN001 Down Syndrome 70 0.079
434
VSC002 Vascular Dementia 58 0.079
435
P GLL020 Gallbladder Disease 64 0.079
436
P PRG013 Paraganglioma 57 0.078
437
P MYS005 Myositis 63 0.078
438
GNR004 Generalized Anxiety Disorder 53 0.078
439
VRC005 Varicose Veins 64 0.078
440
EPD070 Epidermoid Cysts 46 0.077
441
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 54 0.077
442
MNT310 Mental Retardation, X-Linked, Syndromic, Snyder-Robinson Type 32 0.077
443
GND003 Gonadal Disease 32 0.076
444
NVS001 Neovascular Glaucoma 48 0.076
445
FXF002 Fox-Fordyce Disease 40 0.076
446
HMS001 Hemosiderosis 50 0.076
447
PST028 Post-Traumatic Stress Disorder 59 0.076
448
BLD044 Bladder Disease 55 0.076
449
FSC004 Fasciitis 48 0.076
450
c ATR087 Atrial Standstill 1 59 0.076
451
P NMN002 Niemann-Pick Disease 68 0.076
452
CLR108 Colorectal Adenoma 60 0.075
453
c VRL010 Viral Hepatitis 59 0.075
454
IRN002 Iron Metabolism Disease 45 0.075
455
HMR039 Hemorrhage, Intracerebral 57 0.075
456
c PLM022 Pulmonary Valve Insufficiency 38 0.075
457
P MYS003 Myasthenia Gravis 73 0.075
458
FCT002 Factor Xi Deficiency 64 0.074
459
IMM158 Immune Suppression 57 0.074
460
WRN001 Werner Syndrome 70 0.073
461
P DYS021 Dysautonomia 47 0.073
462
DFF003 Diffuse Scleroderma 44 0.073
463
P INT070 Intestinal Obstruction 55 0.073
464
MSC157 Muscular Dystrophy, Duchenne Type 74 0.072
465
PLG002 Plague 55 0.072
466
CRB085 Cerebral Hemorrhage 47 0.072
467
DFC004 Deficiency Anemia 62 0.071
468
P ATX030 Ataxia-Telangiectasia 80 0.071
469
APP008 Appendicitis 64 0.071
470
INT051 Intussusception 51 0.071
471
P PRD006 Prader-Willi Syndrome 66 0.071
472
HDR003 Hidradenitis 47 0.071
473
c MYS011 Myasthenia Gravis Congenital 28 0.071
474
P SCK002 Sick Sinus Syndrome 53 0.071
475
P CYS018 Cystitis 57 0.070
476
P HYP083 Hypopituitarism 59 0.070
477
IRN001 Iron Deficiency Anemia 55 0.070
478
RST001 Restless Legs Syndrome 54 0.070
479
P ALG028 Alagille Syndrome 1 68 0.070
480
c MCR129 Microvascular Complications of Diabetes 1 62 0.070
481
c HRD002 Hereditary Angioedema 59 0.070
482
P SCL057 Scoliosis, Isolated 1 28 0.069
483
MTB004 Metabolic Acidosis 49 0.069
484
c BLM008 Bulimia Nervosa 2 53 0.069
485
FCT007 Factor Vii Deficiency 62 0.069
486
SXL003 Sexual Disorder 45 0.069
487
UNV002 Univentricular Heart 29 0.069
488
ALP103 Alpha-1-Antitrypsin Deficiency 60 0.068
489
HDR002 Hidradenitis Suppurativa 54 0.068
490
P HRD011 Hereditary Spherocytosis 55 0.068
491
BLD053 Blood Platelet Disease 45 0.068
492
SCH012 Schizoaffective Disorder 51 0.068
493
RHM001 Rheumatic Fever 59 0.067
494
c MLG069 Malignant Hypertension 49 0.067
495
RHM035 Rheumatic Fever-Related Antigen 34 0.067
496
c PRM005 Primary Hyperparathyroidism 59 0.066
497
c JVN010 Juvenile Rheumatoid Arthritis 71 0.066
498
PHC013 Phaeochromocytoma 44 0.066
499
ACT119 Acute Promyelocytic Leukemia 64 0.066
500
CMP010 Complex Regional Pain Syndrome 58 0.066
501
P PLY041 Polymyositis 57 0.065
502
c INH004 Inherited Blood Coagulation Disease 29 0.065
503
SPN019 Spondylolisthesis 55 0.065
504
URT037 Urethral Stricture 35 0.064
505
RBS001 Rabies 63 0.064
506
c MCR112 Microvascular Complications of Diabetes 2 30 0.064
507
KRT001 Keratoconjunctivitis Sicca 63 0.064
508
NWB001 Newborn Respiratory Distress Syndrome 56 0.064
509
HMG002 Hemoglobinuria 52 0.064
510
TRN012 Transient Global Amnesia 40 0.063
511
P AST055 Asthma-Related Traits 1 18 0.063
512
RTR011 Retroperitoneal Fibrosis 43 0.063
513
P CLS010 Cluster Headache 47 0.062
514
DBT084 Diabetes Mellitus, Ketosis-Prone 50 0.062
515
HST009 Histiocytoma 51 0.062
516
KLP010 Klippel-Trenaunay-Weber Syndrome 60 0.062
517
MST005 Mastitis 56 0.062
518
SPT004 Septic Arthritis 60 0.062
519
ICH054 Ichthyosis, X-Linked 59 0.062
520
NPH009 Nephrolithiasis 57 0.062
521
HYP005 Hypokalemia 53 0.061
522
RSP007 Respiratory Distress Syndrome, Infant 28 0.061
523
ECH003 Echinococcosis 57 0.061
524
VTM002 Vitamin B12 Deficiency 46 0.060
525
PTT009 Pituitary Gland Disease 56 0.060
526
LGG001 Legg-Calve-Perthes Disease 59 0.060
527
CHR066 Chronic Fatigue Syndrome 67 0.060
528
CRB031 Cerebral Arterial Disease 27 0.060
529
LPT001 Leptospirosis 64 0.060
530
QDR001 Quadriplegia 54 0.060
531
LYM021 Lymphadenitis 62 0.060
532
FBR003 Fibrous Histiocytoma 46 0.060
533
HYP008 Hypertensive Retinopathy 39 0.059
534
CVR006 Cavernous Hemangioma 48 0.059
535
NRM004 Neuroma 51 0.059
536
THY111 Thyroid Carcinoma, Familial Medullary 63 0.059
537
PCK003 Pick Disease of Brain 66 0.059
538
PPL059 Popliteal Pterygium Syndrome, Lethal Type 37 0.059
539
P KLP003 Klippel-Feil Syndrome 46 0.058
540
P HMP002 Hemophagocytic Lymphohistiocytosis 67 0.058
541
NCR007 Necrotizing Fasciitis 49 0.058
542
P SHR001 Short Bowel Syndrome 52 0.058
543
FCT001 Factor Viii Deficiency 50 0.058
544
HDG004 Hodgkin's Granuloma 28 0.058
545
ADR054 Adrenocortical Carcinoma, Hereditary 63 0.058
546
ERY004 Erysipelas 43 0.057
547
P LPD010 Lipodystrophy 57 0.057
548
HDG006 Hodgkin's Paragranuloma 21 0.057
549
CNT060 Central Serous Chorioretinopathy 45 0.057
550
WBR001 Weber Syndrome 40 0.057
551
CST005 Castleman Disease 44 0.057
552
CHK001 Chikungunya 61 0.057
553
CHR005 Chorioamnionitis 52 0.057
554
HYP730 Hypogonadotropic Hypogonadism 56 0.057
555
ANR010 Aneurysm of Sinus of Valsalva 29 0.057
556
P HYP024 Hypoparathyroidism 55 0.056
557
PLR008 Pleurisy 52 0.056
558
PRT029 Parathyroid Adenoma 50 0.056
559
P OMP004 Omphalocele 51 0.056
560
P BCT020 Bacteremia 2 34 0.056
561
RCT018 Rectal Neoplasm 53 0.056
562
PNM001 Pneumocystosis 55 0.056
563
BLD138 Blood Group--Diego System 18 0.056
564
ATN002 Autonomic Nervous System Disease 51 0.056
565
SMT004 Smith-Lemli-Opitz Syndrome 70 0.056
566
c CNT015 Central Sleep Apnea 45 0.055
567
OST097 Osteoporotic Fracture 41 0.055
568
PRP083 Porphyria, Acute Intermittent 60 0.055
569
c ART115 Aortic Valve Disease 1 51 0.055
570
PLR022 Pleural Disease 54 0.055
571
PRP009 Peripartum Cardiomyopathy 53 0.055
572
TYP007 Typhoid Fever 67 0.055
573
P OST009 Osteochondritis Dissecans 58 0.055
574
GGN002 Gigantism 36 0.054
575
SPP008 Suppurative Otitis Media 50 0.054
576
c GLL024 Gallbladder Disease 1 39 0.054
577
STS003 Sitosterolemia 58 0.054
578
c OPT051 Opitz Gbbb Syndrome, Type I 47 0.054
579
PST095 Post-Thrombotic Syndrome 52 0.054
580
CNT047 Contact Dermatitis 64 0.054
581
P MGR003 Migraine with Aura 56 0.054
582
PRN019 Perinatal Necrotizing Enterocolitis 56 0.053
583
PRK066 Parkinsonism with Spasticity, X-Linked 31 0.053
584
PLY150 Polykaryocytosis Inducer 20 0.053
585
P LCT001 Lactic Acidosis 51 0.053
586
CMM005 Common Cold 62 0.053
587
ACH004 Achondroplasia 67 0.053
588
LYM007 Lymphangioleiomyomatosis 68 0.052
589
WRN005 Wrinkles 41 0.052
590
PLM151 Pulmonary Arteriovenous Fistulas 33 0.052
591
P FRG001 Fragile X Syndrome 69 0.052
592
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 53 0.051
593
c GLY003 Glycogen Storage Disease Iii 56 0.051
594
ACL001 Acalculous Cholecystitis 39 0.051
595
PLR005 Pleuropneumonia 47 0.051
596
CMP035 Complete Atrioventricular Canal 27 0.051
597
EBS001 Ebstein Anomaly 52 0.051
598
VND007 Van Der Woude Syndrome 1 57 0.051
599
HYP264 Hypertonia 32 0.050
600
P WSK001 Wiskott-Aldrich Syndrome 76 0.049
601
CRM001 Crimean-Congo Hemorrhagic Fever 58 0.049
602
P GST049 Gastrointestinal System Cancer 60 0.049
603
DDN007 Duodenal Disease 38 0.049
604
TCD001 Tic Disorder 54 0.049
605
FTL021 Fetal Macrosomia 46 0.049
606
P CHR285 Chronic Myelomonocytic Leukemia 63 0.049
607
c ATM022 Autoimmune Myocarditis 40 0.049
608
NTR018 Neutrophilia, Hereditary 46 0.049
609
c HYP057 Hypervitaminosis D 40 0.049
610
c EPS042 Episodic Ataxia, Type 1 57 0.048
611
INF058 Inflammatory Myofibroblastic Tumor 49 0.048
612
ARL004 Aural Atresia, Congenital 27 0.048
613
MYC013 Mycobacterium Abscessus 45 0.048
614
SPL007 Splenic Abscess 29 0.048
615
PLN006 Poland Syndrome 50 0.048
616
ACS001 Acoustic Neuroma 60 0.048
617
P LCT002 Lactose Intolerance 48 0.048
618
PTT046 Pituitary Hormone Deficiency, Combined, 2 57 0.047
619
c SVR056 Severe Hemophilia a 46 0.047
620
P BLM007 Bulimia Nervosa 1 53 0.047
621
GST007 Gastric Dilatation 32 0.047
622
CND006 Candida Glabrata 38 0.047
623
MST019 Mastoiditis 33 0.047
624
MNN021 Meningococcemia 43 0.047
625
HLT001 Holt-Oram Syndrome 61 0.046
626
FML330 Familial Lcat Deficiency 37 0.046
627
PLM052 Pulmonary Arteriovenous Malformation 35 0.045
628
CRS001 Crescentic Glomerulonephritis 44 0.045
629
HRW001 Hair Whorl 31 0.045
630
P FCS012 Facioscapulohumeral Muscular Dystrophy 1 56 0.045
631
PRM013 Premature Menopause 45 0.045
632
P GLL022 Guillain-Barre Syndrome 61 0.044
633
c ACQ014 Acquired Hemophilia 51 0.044
634
P HYP120 Hypoaldosteronism 40 0.043
635
PRP032 Porphyria Variegata 54 0.043
636
c VRL017 Viral Hemorrhagic Fever 37 0.042
637
MLT113 Multicentric Castleman Disease 49 0.042
638
P EPD009 Epidermolysis Bullosa Dystrophica 59 0.042
639
DMP001 Dumping Syndrome 45 0.041
640
CNT105 Central Core Disease of Muscle 57 0.041
641
CRS011 Criss-Cross Heart 24 0.041
642
MLR020 Malaria, Mild 23 0.041
643
ADR013 Adrenal Gland Hyperfunction 54 0.041
644
P RNL017 Renal Oncocytoma 49 0.040
645
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 35 0.040
646
c ACQ042 Acquired Hemophilia a 44 0.039
647
MCR225 Macrophage Activation Syndrome 44 0.038
648
OBS037 Obesity-Hypoventilation Syndrome 45 0.038
649
NRG005 Neurogenic Hypertension 29 0.038
650
c HYP795 Hypothyroidism, Congenital, Nongoitrous, 4 45 0.038
651
P MRL001 Meralgia Paresthetica 28 0.037
652
HYP052 Hyperkalemic Periodic Paralysis 57 0.037
653
VBR003 Vibrio Vulnificus Infection 24 0.035
654
c ALZ050 Alzheimer Disease 5 44 0.035
655
c DNR003 Duane Retraction Syndrome 1 34 0.033
656
ANT005 Anteroseptal Myocardial Infarction 24 0.033
657
INT276 Interatrial Communication 22 0.032
658
MRN002 Mooren's Ulcer 39 0.031
659
P KLF001 Kleefstra Syndrome 36 0.031
660
c ATR062 Atrial Septal Defect 1 32 0.031
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