Search results for Epinephrine

2006 hits were found for Epinephrine

# Family MCID Name MIFTS Score
1
P CRD119 Cardiac Arrest 67 30.911
2
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 22.846
3
PNG002 Pain Agnosia 51 20.038
4
HYP056 Hypoglycemia 65 18.734
5
FDL002 Food Allergy 47 14.027
6
P PHC003 Pheochromocytoma 69 13.875
7
BRN002 Bronchiolitis 57 13.143
8
ADR040 Adrenal Gland Pheochromocytoma 46 12.457
9
TXC005 Toxic Shock Syndrome 62 12.144
10
HYP066 Hyperglycemia 61 11.468
11
PLP001 Pulpitis 48 10.452
12
PPT005 Peptic Ulcer Disease 58 10.188
13
CRP002 Croup 42 10.160
14
c HYP595 Hypertension, Essential 85 9.643
15
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 9.240
16
HYP060 Hyperinsulinism 54 9.121
17
PRT037 Pertussis 65 9.002
18
PLM010 Pulmonary Edema 55 8.512
19
P LNG028 Long Qt Syndrome 64 8.120
20
P OPN001 Open-Angle Glaucoma 55 7.953
21
CRD137 Cardiogenic Shock 56 7.948
22
c TYP008 Type 1 Diabetes Mellitus 70 7.852
23
P ANG015 Angioedema 56 7.803
24
HYP005 Hypokalemia 55 7.781
25
P AST005 Asthma 76 7.578
26
c ATR087 Atrial Standstill 1 74 7.183
27
SYN036 Syncope 45 7.160
28
c ACT249 Acute Asthma 40 6.870
29
ALL029 Allergic Disease 59 6.750
30
P PNC044 Pancreatitis 61 6.672
31
ISC004 Ischemia 61 6.621
32
P RHN004 Rhinitis 57 6.465
33
P URT039 Urticaria 58 6.445
34
c ACT075 Acute Myocardial Infarction 56 6.285
35
PNT038 Peanut Allergy 46 6.225
36
P MYC007 Myocardial Infarction 70 6.199
37
ACR008 Acrocallosal Syndrome 70 6.010
38
CRD223 Cardiac Arrhythmia 63 6.003
39
P CTR002 Cataract 60 5.952
40
PRT058 Pure Autonomic Failure 58 5.903
41
MTB004 Metabolic Acidosis 48 5.888
42
INT323 Intraocular Pressure Quantitative Trait Locus 64 5.860
43
ALL003 Allergic Rhinitis 67 5.846
44
48X005 48,xyyy 39 5.802
45
OCL006 Ocular Hypertension 53 5.799
46
CHL014 Cholera 62 5.722
47
c FML191 Familial Long Qt Syndrome 55 5.664
48
P LCT001 Lactic Acidosis 51 5.514
49
CRD132 Cardiac Conduction Defect 60 5.511
50
LPP008 Lipoprotein Quantitative Trait Locus 65 5.508
51
ATN004 Autonomic Neuropathy 42 5.420
52
ATN005 Autonomic Dysfunction 46 5.391
53
BRK012 Broken Heart Syndrome 42 5.332
54
c ACT027 Acute Pancreatitis 60 5.274
55
P DDN001 Duodenal Ulcer 53 5.214
56
P HYP086 Hypothyroidism 69 5.210
57
P HYP076 Hyperthyroidism 53 5.115
58
HYP266 Hypoxia 57 5.094
59
ACT058 Active Peptic Ulcer Disease 56 4.823
60
47X002 47,xyy 48 4.814
61
c GLC092 Glaucoma, Primary Open Angle 62 4.705
62
P BRS047 Breast Cancer 98 4.704
63
c PNS012 Paine Syndrome 60 4.671
64
c ACT071 Acute Kidney Failure 60 4.626
65
P EXN002 Exanthem 58 4.589
66
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 4.523
67
c LNG047 Long Qt Syndrome 2 59 4.498
68
ART140 Arteries, Anomalies of 53 4.465
69
CNG034 Congestive Heart Failure 69 4.441
70
P TRM003 Tremor 48 4.426
71
c DLT002 Dilated Cardiomyopathy 78 4.426
72
c EPS039 Episodic Pain Syndrome, Familial, 1 42 4.369
73
P NRP001 Neuropathy 60 4.350
74
GLC003 Glucose Intolerance 54 4.274
75
P DBT009 Diabetes Mellitus 67 4.259
76
P ANR048 Aniridia 1 64 4.199
77
OCL069 Ocular Motor Apraxia 57 4.186
78
P RSP003 Respiratory Failure 74 4.073
79
c LNG048 Long Qt Syndrome 3 53 4.036
80
AMN003 Amnestic Disorder 54 4.022
81
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 4.014
82
ANG054 Angina Pectoris 66 3.993
83
AGN016 Aging 54 3.964
84
P NRB001 Neuroblastoma 66 3.937
85
P PTS002 Ptosis 52 3.922
86
P HRT032 Heart Disease 81 3.902
87
PST028 Post-Traumatic Stress Disorder 59 3.893
88
ADN018 Adenoma 59 3.876
89
c TYP009 Type 2 Diabetes Mellitus 92 3.858
90
CYT002 Cytokine Deficiency 43 3.831
91
c HYP836 Hypercholesterolemia, Familial, 1 73 3.807
92
THR024 Thrombosis 56 3.804
93
P HYP040 Hypospadias 51 3.796
94
CRN019 Coronary Artery Vasospasm 47 3.765
95
MCL006 Macular Retinal Edema 57 3.763
96
P MLT074 Multiple Endocrine Neoplasia 59 3.760
97
GST023 Gastric Ulcer 52 3.759
98
ASP030 Aspirin Resistance 40 3.730
99
P SCK005 Sickle Cell Disease 56 3.720
100
MYM001 Myoma 54 3.694
101
P PRG013 Paraganglioma 57 3.680
102
P PLM037 Pulmonary Hypertension 72 3.638
103
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 3.582
104
RST023 Resting Heart Rate, Variation in 40 3.572
105
P ORT004 Orthostatic Intolerance 63 3.542
106
P PNC025 Panic Disorder 52 3.531
107
P DRM053 Dermatitis, Atopic 65 3.509
108
ANX004 Anoxia 40 3.496
109
DYS073 Dysphagia 53 3.492
110
PRS045 Prostatic Hypertrophy 53 3.464
111
P HRP006 Herpes Simplex 65 3.456
112
PLM033 Pulmonary Embolism 58 3.434
113
PRS129 Prostatic Hyperplasia, Benign 49 3.384
114
PRS021 Prostatic Adenoma 43 3.384
115
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 3.368
116
P VSC007 Vascular Disease 63 3.335
117
P SLP006 Sleep Apnea 69 3.332
118
P VNW001 Von Willebrand's Disease 65 3.306
119
P MST009 Mastocytosis 64 3.302
120
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 3.261
121
PRT036 Peritonitis 65 3.261
122
P THY032 Thyroiditis 57 3.244
123
MNT002 Mental Depression 57 3.241
124
TTN003 Tetanus 65 3.241
125
ATR057 Atrioventricular Block 54 3.210
126
END086 End Stage Renal Disease 52 3.202
127
P PRD008 Periodontitis 64 3.197
128
OST012 Osteoarthritis 77 3.180
129
P MYC008 Myocarditis 59 3.168
130
PNM008 Pneumothorax 54 3.164
131
LPD008 Lipid Metabolism Disorder 62 3.163
132
LMY002 Leiomyoma 51 3.155
133
NTL004 Nut Allergy 37 3.143
134
ALC007 Alcohol Dependence 66 3.140
135
INT007 Intermediate Coronary Syndrome 54 3.135
136
P HDC001 Headache 57 3.127
137
P KDN018 Kidney Disease 72 3.122
138
P BLD124 Bleeding Disorder, Platelet-Type, 11 67 3.120
139
PRS063 Paresthesia 39 3.112
140
IGR001 Ige Responsiveness, Atopic 59 3.103
141
TRM010 Traumatic Brain Injury 51 3.099
142
ACT084 Acute Stress Disorder 54 3.099
143
URM002 Uremia 47 3.091
144
ANX010 Anxiety 70 3.091
145
c MLT160 Multiple Endocrine Neoplasia, Type Iia 67 3.079
146
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 3.071
147
RPD005 Rapidly Involuting Congenital Hemangioma 46 3.038
148
MYC005 Myocardial Stunning 46 3.034
149
P SCL018 Scoliosis 57 3.010
150
MLG157 Malignant Pheochromocytoma 36 3.006
151
P THR014 Thrombocytopenia 66 2.991
152
P CRP001 Carpal Tunnel Syndrome 66 2.978
153
DBT002 Diabetic Autonomic Neuropathy 41 2.976
154
HRW001 Hair Whorl 35 2.954
155
c MGR028 Migraine with or Without Aura 1 64 2.953
156
CRN017 Coronary Thrombosis 46 2.946
157
CRB039 Cerebrovascular Disease 66 2.944
158
P ATR011 Atrial Fibrillation 66 2.924
159
MYF001 Myofibroma 42 2.916
160
VRC005 Varicose Veins 60 2.913
161
GLM045 Glioma 63 2.902
162
HDN002 Head Injury 44 2.897
163
P TRN020 Turner Syndrome 67 2.887
164
CYN002 Cyanosis, Transient Neonatal 43 2.886
165
ESP021 Esophageal Cancer 83 2.885
166
DRM006 Dermatitis 62 2.885
167
EGG001 Egg Allergy 41 2.880
168
GLL048 Glial Tumor 52 2.876
169
c PRC016 Pre-Eclampsia 65 2.869
170
ALL006 Allergic Asthma 56 2.861
171
BRN071 Brain Injury 50 2.861
172
P ADL010 Adult Respiratory Distress Syndrome 71 2.848
173
STT002 Status Asthmaticus 49 2.846
174
ACT088 Acute Insulin Response 39 2.839
175
CRN030 Coronary Stenosis 50 2.839
176
P SZR006 Seizure Disorder 70 2.836
177
c THR092 Thrombophilia Due to Thrombin Defect 74 2.822
178
LRY004 Laryngotracheitis 33 2.814
179
LVR012 Liver Cirrhosis 63 2.810
180
RYN005 Raynaud Phenomenon 45 2.810
181
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 2.748
182
PRP007 Priapism 47 2.742
183
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 2.738
184
P ECL001 Eclampsia 52 2.730
185
ENT011 Enterocolitis 55 2.714
186
DSS009 Disseminated Intravascular Coagulation 57 2.714
187
THR035 Thrombasthenia 48 2.714
188
P HYP050 Hyperinsulinemic Hypoglycemia 57 2.709
189
CLF027 Cleft Palate, Isolated 64 2.708
190
MCR011 Microinvasive Gastric Cancer 41 2.708
191
P DBT005 Diabetes Insipidus 54 2.695
192
PTT037 Pituitary Tumors 44 2.695
193
RHB024 Rhabdomyosarcoma 2 67 2.685
194
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 2.667
195
THY030 Thyroid Gland Disease 50 2.667
197
DWN001 Down Syndrome 70 2.652
198
EXR007 Exercise-Induced Anaphylaxis 23 2.632
199
THY029 Thyroid Carcinoma 51 2.631
200
P CNJ013 Conjunctivitis 66 2.622
201
P ENC018 Encephalopathy 62 2.591
202
MLK006 Milk Allergy 47 2.589
203
P LRY019 Laryngitis 53 2.585
204
ING001 Inguinal Hernia 59 2.554
205
P CYS018 Cystitis 59 2.548
206
P DYS154 Dystonia 64 2.533
207
P OVR042 Ovarian Cancer 88 2.529
208
IMP005 Impotence 52 2.520
209
PRP030 Purpura 54 2.515
210
PST092 Posttransplant Acute Limbic Encephalitis 28 2.514
211
P ART021 Arteriosclerosis 54 2.499
212
NNL005 Non-Alcoholic Fatty Liver Disease 63 2.483
213
LYM027 Lymphopenia 56 2.483
214
CRC021 Carcinosarcoma 64 2.481
215
QBC001 Quebec Platelet Disorder 44 2.473
216
P NTR004 Neutropenia 63 2.467
217
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 2.461
218
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 2.461
219
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 2.461
220
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 2.461
221
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 2.461
222
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 2.461
223
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 2.461
224
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 2.461
225
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 2.461
226
SYS004 Systemic Mastocytosis 63 2.452
227
PRN019 Perinatal Necrotizing Enterocolitis 60 2.452
228
MLL004 Mallory-Weiss Syndrome 22 2.449
229
HMN044 Human Immunodeficiency Virus Type 1 78 2.447
230
PLM129 Pulmonary Disease, Chronic Obstructive 74 2.447
231
c GRV008 Graves Disease 1 54 2.433
232
c CHR684 Chronic Kidney Disease 69 2.433
233
HRT011 Heart Septal Defect 49 2.431
234
STR067 Stroke, Ischemic 80 2.427
235
P ART022 Arthritis 71 2.427
236
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 2.421
237
EPG003 Epiglottitis 33 2.421
238
P MYP004 Myopathy 67 2.421
239
PRT013 Portal Hypertension 59 2.421
240
c PRG043 Progressive Familial Heart Block, Type Ib 54 2.419
241
CRH001 Crohn's Disease 80 2.412
242
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 2.411
243
CHL068 Cholestasis 61 2.356
244
P FML187 Familial Hypertension 34 2.356
245
BRN056 Bronchopulmonary Dysplasia 56 2.356
246
P ESS003 Essential Thrombocythemia 69 2.355
247
SQM006 Squamous Cell Carcinoma 60 2.340
248
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 2.335
249
c ORT011 Orthostatic Hypotension 1 43 2.332
250
STC016 Sticky Platelet Syndrome 23 2.325
251
SPN186 Spinal Cord Injury 61 2.312
252
P CRN300 Coronary Heart Disease 1 73 2.312
253
ART016 Aortic Aneurysm 68 2.291
254
TRN015 Transient Cerebral Ischemia 63 2.289
255
c ORT012 Orthostatic Hypotension 2 20 2.286
256
ACR007 Acromegaly 70 2.283
257
DPR016 Depression 65 2.273
258
P ATT013 Attention Deficit-Hyperactivity Disorder 64 2.264
259
c HRD002 Hereditary Angioedema 62 2.254
260
HYP020 Hyperprolactinemia 63 2.253
261
CRC006 Carcinoid Syndrome 55 2.253
262
BLP006 Blepharoconjunctivitis 33 2.253
263
SKN016 Skin Disease 63 2.240
264
VNH007 Von Hippel-Lindau Syndrome 73 2.233
265
BLD053 Blood Platelet Disease 51 2.233
266
P NRF002 Neurofibromatosis 57 2.233
267
GNG013 Gingivitis 59 2.233
268
PRS030 Persistent Fetal Circulation Syndrome 49 2.219
269
VRS002 Virus-Associated Trichodysplasia Spinulosa 30 2.218
270
P CRC039 Coarctation of Aorta 46 2.215
271
DPM001 Dopamine Beta-Hydroxylase Deficiency 53 2.205
272
DLF001 Dieulafoy Lesion 31 2.200
273
CNS004 Constipation 56 2.200
274
P INF037 Inflammatory Bowel Disease 53 2.186
275
P BRG001 Brugada Syndrome 69 2.176
276
P GLM040 Glioma Susceptibility 1 71 2.176
277
CRB037 Cerebral Palsy 67 2.176
278
c PRG042 Progressive Familial Heart Block, Type Ia 66 2.173
279
OST062 Osteoarthritis with Mild Chondrodysplasia 47 2.172
280
PPL052 Papillomatosis, Confluent and Reticulated 34 2.168
281
DSS032 Disease by Infectious Agent 55 2.168
282
EXT054 Extra-Adrenal Pheochromocytoma 32 2.168
283
HYP014 Hyperuricemia 51 2.166
284
THR004 Thrombocytosis 53 2.152
285
P SNS001 Sensorineural Hearing Loss 59 2.145
286
HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 60 2.143
287
P THL005 Thalassemia 56 2.136
288
PST011 Pustulosis of Palm and Sole 52 2.136
289
ACQ007 Acquired Immunodeficiency Syndrome 59 2.136
290
THY111 Thyroid Carcinoma, Familial Medullary 67 2.135
291
P VNT002 Ventricular Septal Defect 58 2.135
292
THY125 Thyroid Gland Medullary Carcinoma 48 2.135
293
P HYP061 Hypertrophic Cardiomyopathy 69 2.131
294
SQM013 Squamous Cell Carcinoma, Head and Neck 73 2.123
295
SCK003 Sickle Cell Anemia 74 2.120
296
RTR001 Retrograde Amnesia 41 2.120
297
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 2.107
298
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 2.107
299
P SCK002 Sick Sinus Syndrome 55 2.107
300
P ATR010 Atrial Heart Septal Defect 58 2.095
301
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 2.091
302
GSG001 Gas Gangrene 52 2.089
303
BRN038 Bronchial Disease 51 2.082
304
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 2.068
305
P PLY018 Polycythemia 56 2.068
306
CYS001 Cystic Fibrosis 78 2.066
307
DBT084 Diabetes Mellitus, Ketosis-Prone 60 2.066
308
TRC020 Tracheitis 43 2.066
309
P VSC011 Vasculitis 61 2.066
310
P MLG056 Malignant Hyperthermia 66 2.066
311
P ALC033 Alcohol Use Disorder 61 2.056
312
ANR007 Anorexia Nervosa 60 2.052
313
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 2.052
314
PNC085 Penicillin Allergy 43 2.052
315
P MJR001 Major Depressive Disorder 68 2.052
316
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 2.052
317
P SLP005 Sleep Disorder 61 2.052
318
AND005 Androgen Insensitivity Syndrome, Mild 21 2.049
319
P HMR005 Hemorrhoid 49 2.044
320
MTR002 Mitral Valve Insufficiency 52 2.042
321
CCN002 Cocaine Abuse 49 2.042
322
P CHR345 Chronic Pain 50 2.042
323
MCS002 Mucositis 56 2.034
324
P PLY011 Polycystic Ovary Syndrome 57 2.031
325
P ACT105 Acute Mountain Sickness 52 2.031
326
WTH001 Withdrawal Disorder 48 2.028
327
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 2.028
328
P PRS040 Prostate Cancer 95 2.008
329
P HMN010 Hemangioma 62 2.008
330
P ART005 Arteriovenous Malformation 65 2.008
331
ANT039 Antisynthetase Syndrome 55 1.996
332
P PRK039 Parkinsonism 55 1.994
333
ANG049 Angioedema Induced by Ace Inhibitors 40 1.993
334
AGG012 Aggressive Nk-Cell Leukemia 46 1.992
335
P CHL066 Cholangitis 52 1.987
336
GLN010 Glanzmann Thrombasthenia 66 1.967
337
INT075 Intracranial Hypertension 53 1.962
338
CHR066 Chronic Fatigue Syndrome 60 1.962
339
END040 Endogenous Depression 55 1.962
340
CMM005 Common Cold 56 1.962
341
c THR090 Thrombocythemia 1 50 1.961
342
P PTN014 Patent Ductus Arteriosus 1 59 1.957
343
ATR089 Atrioventricular Dissociation 21 1.951
344
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 1.934
345
PRP027 Peripheral Vascular Disease 71 1.930
346
P ATS364 Autism 69 1.919
347
DFC004 Deficiency Anemia 74 1.919
348
P PTT006 Pituitary Adenoma 55 1.915
349
MDD011 Mood Disorder 62 1.915
350
INS024 Insulin-Like Growth Factor I 78 1.901
351
P CRN026 Corneal Edema 42 1.900
352
GST039 Gastroduodenitis 37 1.883
353
MLG169 Malignant Astrocytoma 57 1.880
354
SBC016 Subacute Delirium 43 1.872
355
RNL114 Renal Cell Carcinoma, Nonpapillary 80 1.865
356
CLF001 Cleft Lip 53 1.865
357
STT001 Status Epilepticus 59 1.865
358
c EXD008 Exudative Vitreoretinopathy 1 71 1.854
359
HMR023 Hemorrhagic Cystitis 43 1.854
360
ART074 Aortic Dissection 53 1.854
361
SHW001 Shwartzman Phenomenon 36 1.854
362
RGH001 Right Bundle Branch Block 47 1.854
363
CLT003 Colitis 63 1.850
364
INS001 Insulinoma 59 1.840
365
P THR015 Thrombophilia 51 1.840
366
BRN004 Brain Edema 54 1.830
367
P NPH012 Nephrotic Syndrome 60 1.828
368
ADL002 Adult Syndrome 70 1.818
369
P BRN019 Bernard-Soulier Syndrome 61 1.818
370
ATH013 Atherosclerosis Susceptibility 63 1.813
371
P RHM011 Rheumatoid Arthritis 82 1.813
372
MSC007 Muscle Hypertrophy 64 1.813
373
BRR014 Barrett Esophagus 66 1.813
374
P EYD002 Eye Disease 57 1.813
375
ENT004 Enthesopathy 51 1.813
376
FBR047 Fibromyalgia 58 1.810
377
SNT005 Sinoatrial Node Disease 47 1.807
378
CNT047 Contact Dermatitis 57 1.807
379
BCK006 Back Pain 47 1.805
380
HPT014 Hepatorenal Syndrome 49 1.803
381
P ART023 Arthropathy 61 1.803
382
P PRP019 Peripheral Nervous System Disease 58 1.799
383
P HYP098 Hypereosinophilic Syndrome 66 1.799
384
QDR001 Quadriplegia 50 1.799
385
NRT001 Neurotic Disorder 56 1.793
386
CNN003 Conn's Syndrome 79 1.761
387
SNG003 Single Ventricular Heart 30 1.759
388
P ADN016 Adenocarcinoma 63 1.759
389
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 1.756
390
BRN024 Bronchitis 67 1.756
391
DDN006 Duodenitis 50 1.752
392
DRG024 Drug Allergy 40 1.746
393
ULC004 Ulcerative Colitis 74 1.738
394
c ATS383 Autosomal Dominant Non-Syndromic Intellectual Disability 1 37 1.738
395
C1N001 C1 Inhibitor Deficiency 43 1.723
396
AYM001 Ayme-Gripp Syndrome 56 1.723
397
P CRV039 Cervicitis 52 1.723
398
P LNG032 Lung Cancer 98 1.712
399
CRT069 Cortical Malformations, Occipital 30 1.712
400
INF034 Infective Endocarditis 54 1.712
401
P END033 Endocarditis 58 1.705
402
SCL003 Social Phobia 48 1.705
403
c SCN052 Secondary Adrenal Insufficiency 36 1.701
404
P ALZ034 Alzheimer Disease 87 1.701
405
P PNC035 Pancreatic Cancer 86 1.701
406
LPT014 Leptin Deficiency or Dysfunction 78 1.701
407
APN008 Apnea, Obstructive Sleep 67 1.701
408
SDD001 Sudden Infant Death Syndrome 60 1.666
409
PLY001 Polycythemia Vera 69 1.666
410
CRN036 Craniopharyngioma 64 1.666
411
PPT002 Peptic Ulcer Perforation 34 1.666
412
HLX001 Helix Syndrome 48 1.666
413
CLN015 Colon Adenocarcinoma 65 1.666
414
P EPL164 Epilepsy 68 1.666
415
HYP063 Hypersplenism 52 1.651
416
P PRD037 Periodontal Ehlers-Danlos Syndrome 49 1.651
417
ACT098 Acute Erythroid Leukemia 55 1.646
418
LTX001 Latex Allergy 42 1.646
419
P HRN001 Horner's Syndrome 46 1.646
420
ANR040 Aneurysm 61 1.640
421
BHR001 Behr Syndrome 51 1.630
422
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 1.630
423
c DWL002 Dowling-Degos Disease 1 58 1.618
424
HYP540 Hypertension, Diastolic 37 1.618
425
MYL005 Myelofibrosis 71 1.618
426
FML063 Familial Glucocorticoid Deficiency 58 1.618
427
HRT012 Heart Valve Disease 53 1.618
428
c LNG044 Long Qt Syndrome 1 66 1.614
429
c PNC106 Pancreatic Agenesis 1 51 1.610
430
PNC034 Pancreas Disease 50 1.610
431
PPL001 Papillary Adenoma 44 1.610
432
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 1.604
433
c PRM093 Premature Ovarian Failure 7 48 1.598
434
P HYP083 Hypopituitarism 52 1.598
435
P PSR002 Psoriasis 63 1.598
436
MTN003 Motion Sickness 51 1.576
437
SPN035 Spindle Cell Sarcoma 54 1.574
438
SRC014 Sarcoma 65 1.574
439
MNN028 Mononeuropathy of the Median Nerve, Mild 46 1.573
440
GLC084 Glaucoma, Normal Tension 45 1.569
441
SCN049 Second-Degree Atrioventricular Block 33 1.569
442
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 1.569
443
PLT016 Platelet Adenylate Cyclase Activity 16 1.569
444
PLT031 Platelet Membrane Fluidity 28 1.569
445
CRT015 Carotid Artery Occlusion 45 1.569
446
IRR002 Irritable Bowel Syndrome 65 1.569
447
P PHC019 Pheochromocytoma-Paraganglioma 35 1.554
448
P MLT020 Multiple Sclerosis 79 1.554
449
P ART018 Aortic Valve Insufficiency 52 1.554
450
P LVR013 Liver Disease 69 1.554
451
P CRD246 Cardiovascular System Disease 56 1.554
452
URT037 Urethral Stricture 42 1.547
453
OTT002 Otitis Media 71 1.543
454
P SKN015 Skin Carcinoma 71 1.539
455
P LPR021 Leprosy 3 71 1.517
456
LPM012 Lipomatosis, Multiple 60 1.517
457
ADR016 Adrenal Cortical Carcinoma 62 1.517
458
ADR054 Adrenocortical Carcinoma, Hereditary 47 1.517
459
P RTN024 Retinoblastoma 73 1.517
460
OST159 Osteogenic Sarcoma 66 1.517
461
ADR004 Adrenal Cortical Adenocarcinoma 38 1.517
462
PLM005 Pleomorphic Lipoma 40 1.517
463
HYP080 Hypogonadism 50 1.517
464
HNS001 Hansen's Disease 32 1.517
465
BDR001 Bidirectional Tachycardia 14 1.517
466
c ACT134 Acute Liver Failure 59 1.508
467
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 1.508
468
P ALP008 Alopecia 54 1.508
469
P ACN011 Acne 57 1.508
470
HYP835 Hypothalamic Obesity 38 1.503
471
PLY150 Polykaryocytosis Inducer 29 1.502
472
P PLV020 Pelvic Organ Prolapse 58 1.502
473
P END044 Endometriosis 62 1.502
474
c CNG513 Congenital Ptosis 42 1.502
475
PRT010 Parathyroid Carcinoma 68 1.471
476
P GST053 Gastric Cancer 83 1.467
477
INT030 Intracranial Aneurysm 55 1.467
478
P RRT020 Rare Tumor 39 1.466
479
KRT019 Keratitis, Hereditary 66 1.466
480
THR100 Thrombocytopenic Purpura, Autoimmune 61 1.466
481
FST010 Fasting Hypoglycemia 33 1.465
482
P HML001 Hemolytic-Uremic Syndrome 52 1.463
483
P RBL001 Rubella 58 1.463
484
PRN009 Paranoid Schizophrenia 49 1.463
485
c MLG069 Malignant Hypertension 46 1.463
486
P BNG032 Benign Mesothelioma 53 1.463
487
c ACQ012 Acquired Angioedema 38 1.463
488
CNT060 Central Serous Chorioretinopathy 38 1.463
489
MSL001 Measles 61 1.463
490
P BPL003 Bipolar Disorder 56 1.460
491
P ESP024 Esophagitis 60 1.460
492
FSH003 Fish Allergy 30 1.451
493
BNR002 Bone Resorption Disease 47 1.426
494
P HYP069 Hyperparathyroidism 62 1.426
495
PLM001 Pulmonary Tuberculosis 69 1.423
496
PLM022 Pulmonary Valve Insufficiency 45 1.423
497
c NNS018 Nonsyndromic Paraganglioma 33 1.411
498
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 1.405
499
PRT251 Proteinuria, Chronic Benign 57 1.405
500
ALL010 Allergic Contact Dermatitis 56 1.405
501
P MMP001 Mumps 57 1.405
502
c MLT159 Multiple Endocrine Neoplasia, Type Iib 61 1.404
503
PLT033 Platelet Signal Processing Defect 9 1.404
504
P MSC005 Muscular Dystrophy 67 1.394
505
GST013 Gastrojejunal Ulcer 41 1.394
506
PRM024 Primary Angle-Closure Glaucoma 39 1.394
507
ART006 Arthus Reaction 40 1.394
508
SPL018 Splenomegaly 49 1.394
509
SPN019 Spondylolisthesis 52 1.387
510
EXR010 Exercise-Induced Bronchoconstriction 34 1.385
511
P TTR001 Tetralogy of Fallot 69 1.385
512
MLT073 Multisystemic Smooth Muscle Dysfunction Syndrome 44 1.384
513
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 64 1.384
514
SWL001 Swallowing Disorders 38 1.384
515
HNT002 Hantavirus Pulmonary Syndrome 55 1.384
516
ATX019 Ataxia with Vitamin E Deficiency 44 1.384
517
LNG099 Lung Disease 62 1.370
518
SHL001 Shoulder Impingement Syndrome 35 1.364
519
GRW007 Growth Hormone Deficiency 46 1.359
520
P LKM002 Leukemia 67 1.359
521
URT001 Urethritis 53 1.358
522
DBT010 Diabetic Neuropathy 54 1.344
523
EPL050 Epilepsy, Partial, with Pericentral Spikes 26 1.343
524
P PRK057 Parkinson Disease, Late-Onset 80 1.343
525
CHR100 Chronic Ulcer of Skin 57 1.343
526
P PLY006 Polydactyly 59 1.343
527
MLD001 Melioidosis 67 1.343
528
P LCT002 Lactose Intolerance 52 1.343
529
c ACT072 Acute Laryngitis 29 1.343
530
MCL003 Macular Holes 44 1.343
531
c ACT076 Acute Myocarditis 47 1.343
532
PLC005 Placental Insufficiency 56 1.343
533
GTR002 Goiter 53 1.343
534
FCL012 Facial Paralysis 49 1.343
535
P OVR046 Ovarian Cyst 46 1.343
536
MCP033 Mucopolysaccharidoses 44 1.343
537
c CNT101 Central Congenital Hypothyroidism 36 1.343
538
DVR002 Diverticulitis 46 1.333
539
TYP007 Typhoid Fever 64 1.315
540
c SCL052 Scleroderma, Familial Progressive 61 1.304
541
c ART101 Aortic Valve Disease 2 66 1.304
542
NRN004 Neuroendocrine Tumor 59 1.304
543
P CLS010 Cluster Headache 42 1.304
544
MNR012 Meniere Disease 56 1.301
545
FTT001 Fatty Liver Disease 62 1.301
546
CDQ001 Cauda Equina Syndrome 37 1.301
547
IRN002 Iron Metabolism Disease 57 1.301
548
c SML038 Small Cell Cancer of the Lung 69 1.297
549
P MTH007 Methemoglobinemia 46 1.297
550
ORL011 Oral Cancer 60 1.297
551
c MCP049 Mucopolysaccharidosis, Type Vii 63 1.278
552
c ATS007 Autism Spectrum Disorder 72 1.278
553
P STR092 Striatal Degeneration, Autosomal Dominant 2 47 1.278
554
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 1.278
555
PHN003 Phenylketonuria 76 1.278
556
P MYP006 Myopia 56 1.278
557
P PRT096 Peritoneal Mesothelioma 49 1.278
558
P FBR017 Fibrosarcoma 56 1.278
559
PRC001 Pericoronitis 26 1.278
560
P PSD015 Pseudohypoparathyroidism 55 1.278
561
DYS009 Dysthymic Disorder 52 1.278
562
PRV004 Periventricular Leukomalacia 52 1.278
563
DMP001 Dumping Syndrome 43 1.278
564
ACC002 Accommodative Spasm 25 1.278
565
PLN005 Palindromic Rheumatism 43 1.278
566
CHL122 Cholesteatoma of Middle Ear 51 1.278
567
NRM004 Neuroma 49 1.278
568
P INS002 in Situ Carcinoma 53 1.278
569
GRN017 Granulocytopenia 42 1.278
570
CRB090 Cerebral Hypoxia 42 1.278
571
P HPT023 Hepatocellular Carcinoma 96 1.267
572
P DXT004 Dextro-Looped Transposition of the Great Arteries 58 1.257
573
P RNV001 Renovascular Hypertension 49 1.257
574
PRP016 Paraplegia 52 1.257
575
OCL010 Ocular Hypotension 37 1.257
576
P HYP265 Hypotonia 42 1.257
577
P ESP035 Esophagitis, Eosinophilic, 1 58 1.247
578
DNT012 Dental Caries 53 1.247
579
SPN027 Spinal Stenosis 59 1.247
580
LYM019 Lymphosarcoma 46 1.247
581
c PRD040 Periodontitis, Chronic 52 1.226
582
STM007 Stomatitis 54 1.226
583
P VNS003 Venous Insufficiency 55 1.225
584
c PSD108 Pseudohypoparathyroidism, Type Ia 65 1.225
585
URT049 Urate Oxidase, Pseudogene 24 1.225
586
ANG018 Angiomyolipoma 46 1.225
587
NRD001 Neurodermatitis 39 1.225
588
ILS001 Ileus 50 1.212
589
P RNL015 Renal Hypertension 45 1.212
590
HMP009 Haemophilus Influenzae 41 1.212
591
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 1.211
592
P CNR004 Cone-Rod Dystrophy 2 74 1.211
593
P MCR129 Microvascular Complications of Diabetes 1 68 1.211
594
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 38 1.211
595
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 40 1.211
596
THY122 Thyroid Gland Cancer 59 1.211
597
CTS005 Catastrophic Antiphospholipid Syndrome 43 1.211
598
CRY008 Cryopyrin-Associated Periodic Syndrome 48 1.211
599
P NRV007 Nervous System Disease 67 1.211
600
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 1.206
601
ACT235 Acute Macular Neuroretinopathy 16 1.206
602
NTR018 Neutrophilia, Hereditary 50 1.206
603
PNM010 Pneumothorax, Primary Spontaneous 58 1.206
604
CHR048 Chronic Rhinitis 46 1.206
605
CRY005 Cryptococcosis 60 1.206
606
SPS004 Spastic Quadriplegia 40 1.206
607
MNN009 Meningoencephalitis 48 1.206
608
VSC002 Vascular Dementia 60 1.206
609
INT146 Intervertebral Disc Disease 63 1.191
610
GST071 Gastrointestinal Carcinoma 46 1.191
611
P MLN008 Melanoma 76 1.191
612
c BSL007 Basal Cell Carcinoma 68 1.191
613
GST050 Gastrointestinal System Disease 55 1.191
614
ALD013 Aldosterone-Producing Adenoma 36 1.185
615
c DPH024 Diaphragmatic Hernia, Congenital 64 1.185
616
ADR041 Adrenal Cortical Adenoma 49 1.185
617
P OPT006 Optic Nerve Disease 58 1.185
618
P MTR012 Mitral Valve Disease 57 1.185
619
P DRR001 Diarrhea 55 1.185
620
P HYP055 Hypoplastic Left Heart Syndrome 65 1.185
621
P HYP750 Hypertriglyceridemia, Familial 62 1.164
622
HPT004 Hepatic Coma 43 1.164
623
CRD001 Cardiac Tamponade 43 1.164
624
c PRM005 Primary Hyperparathyroidism 59 1.164
625
CHL035 Cholinergic Urticaria 29 1.164
626
P HMP007 Hemophilia 52 1.164
627
CRB086 Cerebral Aneurysms 40 1.164
628
P DYS021 Dysautonomia 38 1.164
629
CRV002 Cervix Uteri Carcinoma in Situ 47 1.127
630
CRV045 Cervical Intraepithelial Neoplasia 39 1.127
631
P MYS003 Myasthenia Gravis 68 1.126
632
RTN017 Retinal Detachment 60 1.126
633
TNG007 Tongue Carcinoma 52 1.126
634
ACT003 Acute Kidney Tubular Necrosis 46 1.126
635
EXP004 Exophthalmos 51 1.126
636
P ANT001 Anterolateral Myocardial Infarction 34 1.126
637
P RRH023 Rare Hereditary Hemochromatosis 54 1.126
638
ADR005 Adrenal Carcinoma 62 1.126
639
HMS001 Hemosiderosis 48 1.126
640
CCC002 Coccidiosis 50 1.126
641
NPH010 Nephrosclerosis 50 1.126
642
P TCD001 Tic Disorder 49 1.126
643
GLM008 Glomus Tumor 50 1.126
644
PST053 Postherpetic Neuralgia 40 1.126
645
CLS040 Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency 37 1.126
646
PRS115 Prosthetic Joint Infection 42 1.126
647
c SYS001 Systemic Lupus Erythematosus 87 1.119
648
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 1.119
649
c MJR022 Major Affective Disorder 8 38 1.119
650
P LKM062 Leukemia, Acute Lymphoblastic 69 1.119
651
c MJR024 Major Affective Disorder 9 41 1.119
652
P ACT092 Acth-Independent Macronodular Adrenal Hyperplasia 56 1.119
653
P STR020 Strabismus 56 1.119
654
CMP010 Complex Regional Pain Syndrome 60 1.119
655
MCH006 Mechanical Strabismus 40 1.119
656
P MYL006 Myeloid Leukemia 61 1.119
657
P PRS038 Personality Disorder 65 1.119
658
DSS008 Disease of Mental Health 74 1.119
659
ISL003 Isolated Growth Hormone Deficiency 57 1.119
660
P BND020 Bone Disease 59 1.119
661
P SBS003 Substance Abuse 54 1.119
662
AMN001 Amenorrhea 54 1.119
663
P HYP120 Hypoaldosteronism 35 1.119
664
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 61 1.118
665
FML159 Familial Periodic Paralyses 16 1.115
666
HYP017 Hypophosphatemia 49 1.114
667
NRL016 Neural Tube Defects 81 1.114
668
CHG001 Chagas Disease 66 1.114
669
HPT019 Hepatic Encephalopathy 59 1.114
670
ANG011 Angiodysplasia 42 1.114
671
GST033 Gestational Diabetes 61 1.114
672
HYP026 Hypoglycemic Coma 37 1.114
673
FNT004 Fainting 29 1.114
674
MCR359 Macrothrombocytopenia and Granulocyte Inclusions with or Without Nephritis or Sensorineural Hearing Loss 44 1.091
675
TNS005 Tonsillitis 57 1.087
676
NNF008 Non-Functioning Paraganglioma 19 1.068
677
SPR068 Sporadic Pheochromocytoma/secreting Paraganglioma 29 1.068
678
c ERL020 Early-Onset Schizophrenia 44 1.063
679
ATS010 Autosomal Recessive Disease 42 1.063
680
IMM167 Immune Deficiency Disease 78 1.063
681
BCT022 Bacterial Infectious Disease 56 1.063
682
PST048 Postural Orthostatic Tachycardia Syndrome 46 1.063
683
c CHR708 Chronic Urticaria 42 1.063
684
GNG002 Ganglioneuroma 52 1.063
685
GNG005 Gangliocytoma 55 1.063
686
IDP070 Idiopathic Scoliosis 42 1.063
687
GNR004 Generalized Anxiety Disorder 55 1.063
688
P MYT002 Myotonic Dystrophy 51 1.063
689
APP008 Appendicitis 62 1.051
690
OPT003 Opiate Dependence 49 1.051
691
P INT068 Intestinal Disease 53 1.051
692
P BLD134 Bladder Cancer 79 1.048
693
P OST002 Osteoporosis 76 1.048
694
ATM095 Autoimmune Disease 61 1.048
695
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.048
696
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 1.048
697
CVD001 Covid-19 57 1.048
698
URL001 Urolithiasis 46 1.048
699
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 1.048
700
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.048
701
GYN001 Gynecomastia 47 1.048
702
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 1.048
703
SVR001 Severe Acute Respiratory Syndrome 67 1.048
704
PSY004 Psychotic Disorder 66 1.048
705
INF021 Infant Gynecomastia 30 1.048
706
P INF032 Infertility 57 1.048
707
P GLM007 Glomerulonephritis 60 1.048
708
c BRT042 Bartter Syndrome, Type 3 46 1.036
709
DBT092 Diabetes Insipidus, Nephrogenic, X-Linked 38 1.036
710
RYN001 Raynaud Disease 50 1.036
711
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 1.036
712
LNG105 Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome 35 1.036
713
P AMY004 Amyloidosis 70 1.036
714
EXT007 Extracutaneous Mastocytoma 38 1.036
715
VLK001 Volkmann Contracture 23 1.036
716
HMG002 Hemoglobinuria 50 1.036
717
MST004 Mast Cell Neoplasm 42 1.036
718
P SYP003 Syphilis 59 1.036
719
c SCN006 Secondary Syphilis 36 1.036
720
SPL006 Splenic Infarction 37 1.036
721
LFT001 Left Bundle Branch Hemiblock 47 1.036
722
P TBR001 Tuberous Sclerosis 69 1.036
723
P GLY013 Glycogen Storage Disease 60 1.036
724
DPH001 Diphtheria 59 1.036
725
DDN009 Duodenal Obstruction 34 1.036
726
RCT020 Rectum Adenocarcinoma 48 1.036
727
P CLL015 Collagen Disease 48 1.036
728
CRH005 Crohn's Colitis 53 1.022
729
c INF071 Inflammatory Bowel Disease 1 65 1.022
730
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 1.022
731
VGN023 Vaginitis 56 1.022
732
c LKM063 Leukemia, Chronic Myeloid 71 1.008
733
CMP040 Complement Component 4, Partial Deficiency of 34 1.008
734
P MSC003 Muscular Atrophy 52 1.008
735
WHT017 Wheat Allergy 31 1.008
736
RTN020 Retinal Vascular Disease 46 1.008
737
IRN001 Iron Deficiency Anemia 58 1.008
738
P PYL005 Pyelonephritis 57 1.008
739
ESP002 Esophageal Varix 51 1.008
740
P MYC033 Myoclonus 47 1.008
741
PMP014 Pemphigoid 51 0.979
742
P PLM034 Pulmonary Emphysema 58 0.979
743
CHR008 Choroiditis 48 0.979
744
SPS057 Spasticity 42 0.968
745
P PLY014 Polycystic Kidney Disease 69 0.968
746
RHM028 Rheumatic Heart Disease 56 0.968
747
RCK004 Rickets 68 0.968
748
LWC001 Low Compliance Bladder 45 0.968
749
P INT143 Interstitial Cystitis 60 0.968
750
ADR008 Adrenal Adenoma 55 0.968
751
P SCH015 Schizophrenia 74 0.950
752
GST092 Gastroesophageal Reflux 61 0.950
753
PRP080 Peripheral Artery Disease 54 0.950
754
PLL012 Pollen Allergy 45 0.950
755
ZLL002 Zollinger-Ellison Syndrome 55 0.950
756
c ACQ017 Acquired Von Willebrand Syndrome 48 0.950
757
GST030 Gastrinoma 45 0.950
758
P MVM001 Movement Disease 61 0.950
759
P HML002 Hemolytic Anemia 62 0.950
760
CHL067 Cholecystitis 60 0.950
761
CLL003 Cellulitis 53 0.950
762
P HRM001 Hermansky-Pudlak Syndrome 65 0.950
763
QLT001 Qualitative Platelet Defect 29 0.950
764
ASP004 Asphyxia Neonatorum 50 0.950
765
CRT004 Carotid Artery Thrombosis 39 0.950
766
P PLY019 Polyneuropathy 52 0.950
767
P MTR003 Mitral Valve Stenosis 53 0.950
768
CLP006 Clopidogrel Resistance 44 0.950
769
MLT131 Multifocal Atrial Tachycardia 17 0.930
770
CLR108 Colorectal Adenoma 64 0.930
771
DBN001 Dubin-Johnson Syndrome 57 0.930
772
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 54 0.930
773
c TBR025 Tuberous Sclerosis 1 84 0.930
774
MDD018 Middle East Respiratory Syndrome 44 0.930
775
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 43 0.930
776
SBV001 Subvalvular Aortic Stenosis 30 0.930
777
KDN015 Kidney Angiomyolipoma 46 0.930
778
TRN018 Transitional Cell Carcinoma 56 0.930
779
AMP007 Amphetamine Abuse 36 0.930
780
PDP001 Pedophilia 29 0.930
781
PTT004 Pituitary Apoplexy 47 0.930
782
ANG005 Anogenital Venereal Wart 56 0.930
783
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 0.914
784
LWF001 Low-Flow Priapism 16 0.889
785
c PLM164 Pulmonary Hypertension, Primary, 1 76 0.889
786
P LKM071 Leukemia, Chronic Lymphocytic 75 0.889
787
FCT001 Factor Viii Deficiency 60 0.889
788
c MCR115 Microvascular Complications of Diabetes 5 65 0.889
789
c MCR130 Microvascular Complications of Diabetes 6 41 0.889
790
MYL009 Myelodysplastic Syndrome 67 0.889
791
LMB062 Limb Ischemia 55 0.889
792
c CHR711 Chronic Asthma 41 0.889
793
HLC007 Helicobacter Pylori Infection 67 0.889
794
c MCR120 Microvascular Complications of Diabetes 7 47 0.889
795
c HMP029 Hemophilia a 68 0.889
796
MLT157 Multiple System Atrophy 1 69 0.889
797
MST024 Mastocytosis, Cutaneous 67 0.889
798
CLR109 Colorectal Adenocarcinoma 50 0.889
799
INT002 Intermittent Claudication 61 0.889
800
ANR004 Anuria 44 0.889
801
AGR002 Agoraphobia 45 0.889
802
CRB004 Cerebral Artery Occlusion 45 0.889
803
c MCR113 Microvascular Complications of Diabetes 3 52 0.889
804
c MCR133 Microvascular Complications of Diabetes 4 41 0.889
805
CRT013 Carotid Stenosis 51 0.889
806
P HYD006 Hydrocephalus 61 0.889
807
SVR004 Severe Combined Immunodeficiency 72 0.889
808
c FML021 Familial Hypercholesterolemia 72 0.889
809
HYP141 Hyperphenylalaninemia 42 0.889
810
P MNN013 Meningitis 65 0.889
811
HRP004 Herpes Zoster 61 0.889
812
ORL012 Oral Leukoplakia 36 0.889
813
LKP003 Leukoplakia 39 0.889
814
CHR178 Chromosomal Triplication 34 0.889
815
P CRD224 Cardiofaciocutaneous Syndrome 1 71 0.889
816
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 70 0.889
817
NTR005 Nutritional Deficiency Disease 61 0.889
818
NWB001 Newborn Respiratory Distress Syndrome 56 0.889
819
SKN013 Skin Benign Neoplasm 50 0.889
820
DNT014 Dental Pulp Disease 43 0.889
821
c BTT014 Beta-Thalassemia 72 0.878
822
HYP780 Hypoadrenocorticism, Familial 61 0.878
823
P MJR007 Major Affective Disorder 1 42 0.878
824
GST040 Gastric Adenocarcinoma 67 0.878
825
TRC022 Tricuspid Valve Insufficiency 47 0.878
826
P DMN002 Dementia 66 0.878
827
P GRV001 Graves' Disease 55 0.878
828
EPC002 Epicondylitis 44 0.878
829
c INH020 Inherited Metabolic Disorder 48 0.878
830
P PNM007 Pneumonia 67 0.878
831
FSC004 Fasciitis 49 0.878
832
TNS014 Tenosynovitis 46 0.878
833
P PRC019 Precocious Puberty 47 0.878
834
CHR344 Chronic Orthostatic Intolerance 14 0.878
836
CCN009 Cocaine Intoxication 30 0.823
837
PLM061 Pulmonary Edema of Mountaineers 26 0.823
838
P FML018 Familial Mediterranean Fever 73 0.823
839
OBS002 Obsessive-Compulsive Disorder 68 0.823
840
FCL074 Facial Spasm 19 0.823
841
ANS021 Anisocoria 25 0.823
842
c BRN108 Branchiootic Syndrome 1 62 0.823
843
ARM002 Aromatic L-Amino Acid Decarboxylase Deficiency 56 0.823
844
TRG002 Trigeminal Neuralgia 61 0.823
845
PTT046 Pituitary Hormone Deficiency, Combined, 2 62 0.823
846
P HNT016 Huntington Disease 73 0.823
847
c DMN023 Diamond-Blackfan Anemia 1 66 0.823
849
INT394 Intermittent Asthma 21 0.823
850
INF118 Inflammatory Myopathy with Abundant Macrophages 27 0.823
851
WHP002 Whiplash 36 0.823
852
GNG008 Ganglioneuroblastoma 47 0.823
853
PRL008 Paralytic Ileus 45 0.823
854
P GRF003 Graft-Versus-Host Disease 71 0.823
855
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.823
856
MYL031 Myeloproliferative Neoplasm 66 0.823
857
BRC012 Brucellosis 66 0.823
858
PLC009 Placenta Praevia 38 0.823
859
HMP001 Hemopericardium 47 0.823
860
ANH002 Anhidrosis 46 0.823
861
HYP043 Hyperandrogenism 48 0.823
862
P PRC012 Pericardial Effusion 50 0.823
863
EHR002 Ehrlichiosis 39 0.823
864
P RTN018 Retinal Disease 53 0.823
865
PTN001 Patent Foramen Ovale 62 0.823
866
GST037 Gastroparesis 52 0.823
867
MST020 Mast Cell Activation Syndrome 28 0.823
868
BRT037 Brittle Diabetes 24 0.823
869
c BLD140 Blood Group, I System 46 0.791
870
LGH007 Leigh Syndrome 70 0.791
871
c HYP272 Hypercholesterolemia, Familial, 3 45 0.791
872
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 63 0.791
873
MTC112 Mitochondrial Dna-Associated Leigh Syndrome 32 0.791
874
LCR013 Lacrimal Duct Defect 40 0.790
875
c DMN005 Diamond-Blackfan Anemia 2 28 0.790
876
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 55 0.790
877
CHR072 Chordoma 57 0.790
878
INT067 Interstitial Nephritis 46 0.790
879
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.790
880
c PSD117 Pseudohypoparathyroidism, Type Ic 37 0.790
881
P TYR004 Tyrosinemia 50 0.790
882
P CND004 Candidiasis 58 0.790
883
P SYS005 Systemic Scleroderma 74 0.790
884
MRS001 Marasmus 42 0.790
885
CRB016 Carbuncle 39 0.790
886
GST045 Gastroenteritis 58 0.790
887
KWS001 Kwashiorkor 45 0.790
888
NCR001 Necrotizing Ulcerative Gingivitis 26 0.790
889
CLS032 Clostridium Perfringens Infection 16 0.790
890
AMR003 Amaurosis Fugax 33 0.790
891
ALL014 Allergic Encephalomyelitis 34 0.790
892
BRN045 Brunner Syndrome 52 0.779
893
P PRD017 Periodic Paralyses 24 0.779
894
PST021 Postpartum Depression 50 0.771
895
APN006 Apnea of Prematurity 24 0.771
896
P ACT244 Acth-Independent Cushing Syndrome 38 0.771
897
CNG506 Congenital Amyoplasia 27 0.771
898
P VTR007 Vitreoretinopathy 46 0.771
899
P MYC084 Mycobacterium Tuberculosis 1 68 0.771
900
P CLR023 Colorectal Cancer 100 0.771
901
P URN019 Urinary Tract Infection 49 0.771
902
P LYM118 Lymphoma 67 0.771
904
RFL001 Reflex Sympathetic Dystrophy 51 0.771
905
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.771
906
NRR001 Neuroretinitis 42 0.771
907
c PRM340 Primary Adrenal Insufficiency 38 0.771
908
c HPT003 Hepatitis a 63 0.771
909
P LPS004 Lupus Erythematosus 61 0.771
910
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 0.771
911
RTN023 Retinitis 46 0.771
912
c ACT068 Acute Cystitis 61 0.771
913
ALG001 Algoneurodystrophy 38 0.771
914
HGH043 High Grade Glioma 45 0.771
915
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.771
916
CPL003 Capillary Leak Syndrome 54 0.771
917
LGP001 Lagophthalmos 30 0.771
918
PLT032 Platelet Responsiveness to Adrenaline, Depressed 7 0.755
919
PLY100 Polyploidy 36 0.751
920
SCR039 Scorpion Envenomation 41 0.751
921
CHR005 Chorioamnionitis 50 0.751
922
P ANP001 Anaplastic Large Cell Lymphoma 61 0.751
923
PHY008 Physical Urticaria 33 0.751
924
MYL020 Myelomeningocele 51 0.751
925
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 0.751
926
P FTL001 Fetal Alcohol Syndrome 55 0.751
927
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 66 0.751
928
c BRS111 Breast-Ovarian Cancer, Familial 2 53 0.751
929
P SCL057 Scoliosis, Isolated 1 40 0.751
930
GST019 Gastrointestinal Stromal Tumor 78 0.751
931
PTC002 Potocki-Lupski Syndrome 48 0.751
932
c ACT042 Acute Pyelonephritis 45 0.751
933
INT040 Intrinsic Asthma 36 0.751
934
CHR074 Choriocarcinoma 46 0.751
935
P PRD021 Periodic Paralysis 41 0.751
936
P ANT006 Antiphospholipid Syndrome 55 0.751
937
NPH009 Nephrolithiasis 54 0.751
938
P INT070 Intestinal Obstruction 57 0.751
939
P RTN014 Retinal Artery Occlusion 47 0.751
940
ERY003 Erythema Multiforme 56 0.751
941
BRN026 Branch Retinal Artery Occlusion 41 0.751
942
P HMR003 Hemorrhagic Disease 59 0.751
943
CRS013 Crustacean Allergy 21 0.751
944
RBS001 Rabies 58 0.751
945
PRT029 Parathyroid Adenoma 51 0.751
946
PHR003 Pharyngitis 58 0.751
947
c BNG021 Benign Essential Hypertension 35 0.751
948
P CMP008 Compartment Syndrome 50 0.751
949
SYS003 Systolic Heart Failure 49 0.751
950
END051 Endolymphatic Sac Tumor 24 0.751
951
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.715
952
c MCL013 Mucolipidosis Iv 65 0.715
953
AND020 Androgen Insensitivity, Partial 55