Search results for Warfarin

1675 hits were found for Warfarin

# Family MCID Name MIFTS Score
1
CMR002 Coumarin Resistance 59 52.794
2
WRF003 Warfarin Syndrome 29 44.407
3
WRF006 Warfarin Sensitivity, X-Linked 23 35.961
4
P ATR011 Atrial Fibrillation 66 34.982
5
c THR092 Thrombophilia Due to Thrombin Defect 74 23.425
6
THR024 Thrombosis 56 17.274
7
PLM033 Pulmonary Embolism 58 15.834
8
STR067 Stroke, Ischemic 79 13.088
9
TRN015 Transient Cerebral Ischemia 62 10.319
10
c FML001 Familial Atrial Fibrillation 65 10.125
11
CHL070 Cholesterol Embolism 39 9.624
12
VTM033 Vitamin K Deficiency Bleeding 49 9.505
13
CRB039 Cerebrovascular Disease 65 8.710
14
HRT012 Heart Valve Disease 53 8.358
15
CNG034 Congestive Heart Failure 69 8.274
16
P ANT006 Antiphospholipid Syndrome 55 8.156
17
c CHR684 Chronic Kidney Disease 73 8.006
18
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 37 7.733
19
P HRT032 Heart Disease 84 7.516
20
END086 End Stage Renal Disease 54 7.197
21
P KDN018 Kidney Disease 71 6.762
22
P THR014 Thrombocytopenia 66 6.510
23
P MYC007 Myocardial Infarction 69 6.409
24
P VSC007 Vascular Disease 62 6.323
25
ISC004 Ischemia 61 6.005
26
HPR003 Heparin-Induced Thrombocytopenia 47 5.941
27
ACT058 Active Peptic Ulcer Disease 55 5.658
28
48X005 48,xyyy 39 5.640
29
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 5.375
30
ART140 Arteries, Anomalies of 52 5.190
31
P CRN300 Coronary Heart Disease 1 73 5.097
32
P DBT009 Diabetes Mellitus 67 4.883
33
P MTR003 Mitral Valve Stenosis 53 4.872
34
P THR015 Thrombophilia 51 4.846
35
PRT018 Portal Vein Thrombosis 50 4.830
36
c ACT075 Acute Myocardial Infarction 55 4.721
37
LPP008 Lipoprotein Quantitative Trait Locus 65 4.696
38
LVR012 Liver Cirrhosis 62 4.478
39
PRT011 Protein C Deficiency 47 4.473
40
THR016 Thrombophlebitis 50 4.447
41
PRP027 Peripheral Vascular Disease 71 4.435
42
CRT084 Creatinine Clearance Quantitative Trait Locus 25 4.412
43
KRT002 Keratomalacia 54 4.404
44
CRD223 Cardiac Arrhythmia 63 4.136
45
OCL069 Ocular Motor Apraxia 57 4.075
46
AGN016 Aging 53 4.065
47
P TRN020 Turner Syndrome 67 4.010
48
PRP080 Peripheral Artery Disease 54 3.895
49
P BLD124 Bleeding Disorder, Platelet-Type, 11 68 3.868
50
CLC001 Calciphylaxis 50 3.865
51
RHM028 Rheumatic Heart Disease 55 3.810
52
HDN002 Head Injury 44 3.805
53
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 3.780
54
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 3.772
55
PRT014 Protein S Deficiency 46 3.743
56
ANR040 Aneurysm 60 3.634
57
P PLM037 Pulmonary Hypertension 69 3.621
58
P LVR013 Liver Disease 68 3.586
59
P ALZ034 Alzheimer Disease 87 3.532
60
P PST095 Post-Thrombotic Syndrome 51 3.487
61
ATR024 Atrial Fibrillation and Stroke 22 3.457
62
c ATR087 Atrial Standstill 1 74 3.405
63
P CRD246 Cardiovascular System Disease 55 3.355
64
ALL029 Allergic Disease 61 3.310
65
P LPS004 Lupus Erythematosus 61 3.291
66
P CTR002 Cataract 59 3.286
67
INT010 Intracranial Embolism 48 3.271
68
c PLM164 Pulmonary Hypertension, Primary, 1 75 3.247
69
HMP001 Hemopericardium 47 3.239
70
CLC006 Calcinosis 47 3.236
71
c SYS001 Systemic Lupus Erythematosus 85 3.229
72
ADL002 Adult Syndrome 69 3.228
73
c HYP595 Hypertension, Essential 84 3.226
74
P MTR012 Mitral Valve Disease 57 3.203
75
P PRS040 Prostate Cancer 95 3.162
76
P DMN002 Dementia 65 3.158
77
c ART115 Aortic Valve Disease 1 72 3.157
78
CYT018 Cytochrome P450 2d6 Variant 26 3.145
79
c DLT002 Dilated Cardiomyopathy 79 3.137
80
TRM010 Traumatic Brain Injury 50 3.131
81
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 3.089
82
P OST002 Osteoporosis 76 3.089
83
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 3.089
84
CHR466 Chronic Thromboembolic Pulmonary Hypertension 47 2.965
85
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 37 2.958
86
P END033 Endocarditis 58 2.938
87
ATH013 Atherosclerosis Susceptibility 63 2.934
88
P CHN044 Chondrodysplasia Punctata Syndrome 43 2.921
89
P HDC001 Headache 56 2.863
90
c TYP009 Type 2 Diabetes Mellitus 91 2.862
91
c HPT001 Hepatitis C 61 2.845
92
DFC004 Deficiency Anemia 74 2.831
93
RHB024 Rhabdomyosarcoma 2 65 2.825
94
PRP030 Purpura 54 2.825
95
P ART018 Aortic Valve Insufficiency 52 2.823
96
P PRC012 Pericardial Effusion 50 2.814
97
CRD001 Cardiac Tamponade 44 2.793
98
CRH001 Crohn's Disease 80 2.742
99
P ANR048 Aniridia 1 66 2.736
100
PTN001 Patent Foramen Ovale 61 2.732
101
ART016 Aortic Aneurysm 68 2.705
102
PRT013 Portal Hypertension 59 2.701
103
c ART101 Aortic Valve Disease 2 65 2.693
104
LWC001 Low Compliance Bladder 44 2.689
105
c HYP724 Hyperlipoproteinemia, Type Iii 66 2.688
106
INT007 Intermediate Coronary Syndrome 53 2.684
107
P PLM036 Pulmonary Fibrosis 65 2.653
108
P VSC011 Vasculitis 61 2.646
109
P ART022 Arthritis 70 2.604
110
P CRN074 Coronary Artery Aneurysm 41 2.561
111
BLD051 Blood Coagulation Disease 52 2.552
112
BRN071 Brain Injury 50 2.523
113
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 2.517
114
c BLD140 Blood Group, I System 47 2.517
115
DWN001 Down Syndrome 70 2.499
116
PLM134 Pulmonary Fibrosis, Idiopathic 76 2.468
117
CRB009 Cerebritis 43 2.464
118
P HYP076 Hyperthyroidism 53 2.441
119
ATX019 Ataxia with Vitamin E Deficiency 44 2.428
120
DSS009 Disseminated Intravascular Coagulation 56 2.419
121
KWS002 Kawasaki Disease 65 2.413
122
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 2.391
123
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 2.388
124
P HMP007 Hemophilia 52 2.387
125
PRS047 Prostatitis 57 2.378
126
P EXN002 Exanthem 58 2.329
127
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 2.323
128
P RHM011 Rheumatoid Arthritis 81 2.316
129
AND005 Androgen Insensitivity Syndrome, Mild 21 2.313
130
THR089 Thrombophilia Due to Protein S Deficiency, Autosomal Dominant 28 2.312
131
P PRK057 Parkinson Disease, Late-Onset 79 2.293
132
P CRD119 Cardiac Arrest 68 2.283
133
PPT005 Peptic Ulcer Disease 58 2.275
134
c MGR028 Migraine with or Without Aura 1 63 2.273
135
P ALC033 Alcohol Use Disorder 67 2.245
136
CRB004 Cerebral Artery Occlusion 45 2.245
137
HRW001 Hair Whorl 35 2.244
138
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 2.224
139
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 2.200
140
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 2.200
141
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 2.200
142
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 2.200
143
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 2.200
144
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 2.200
145
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 2.200
146
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 2.200
147
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 2.200
148
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 2.200
149
DPR016 Depression 64 2.187
150
FCT001 Factor Viii Deficiency 61 2.161
151
PLM010 Pulmonary Edema 54 2.159
152
MNT002 Mental Depression 56 2.135
153
P FNG006 Feingold Syndrome 1 61 2.129
154
PST011 Pustulosis of Palm and Sole 52 2.120
155
P PSR002 Psoriasis 63 2.120
156
47X002 47,xyy 47 2.108
157
c SCL052 Scleroderma, Familial Progressive 60 2.092
158
c SPN225 Spondyloarthropathy 1 70 2.074
159
LPD008 Lipid Metabolism Disorder 61 2.070
160
49X006 49, Xxxxy Syndrome 40 2.047
161
P HMR003 Hemorrhagic Disease 59 2.034
162
P HYP069 Hyperparathyroidism 62 2.024
163
SCK003 Sickle Cell Anemia 74 2.023
164
P SCK005 Sickle Cell Disease 56 2.017
165
P URN019 Urinary Tract Infection 48 2.012
166
PLM129 Pulmonary Disease, Chronic Obstructive 74 2.008
167
CRD220 Cardiac Valvular Defect, Developmental 29 2.003
168
ANT039 Antisynthetase Syndrome 55 2.003
169
P LNG032 Lung Cancer 98 1.999
170
P NPH012 Nephrotic Syndrome 61 1.994
171
P PNC035 Pancreatic Cancer 87 1.989
172
P HYP750 Hypertriglyceridemia, Familial 61 1.987
173
c ACT071 Acute Kidney Failure 60 1.977
174
PSR001 Psoriatic Arthritis 61 1.974
175
c ACT027 Acute Pancreatitis 60 1.974
176
PRT251 Proteinuria, Chronic Benign 58 1.967
177
P HPT021 Hepatitis 68 1.966
178
VRC005 Varicose Veins 59 1.960
179
P MJR001 Major Depressive Disorder 68 1.947
180
OST012 Osteoarthritis 77 1.947
181
P GLM007 Glomerulonephritis 59 1.940
182
P LYM118 Lymphoma 66 1.932
183
P SHR001 Short Bowel Syndrome 53 1.919
184
IGG001 Iga Glomerulonephritis 50 1.918
185
P PNC044 Pancreatitis 61 1.917
186
HYP063 Hypersplenism 51 1.916
187
P LKD001 Leukodystrophy 58 1.916
188
P HYD006 Hydrocephalus 62 1.915
189
MTR002 Mitral Valve Insufficiency 51 1.905
190
c SML038 Small Cell Cancer of the Lung 68 1.899
191
LYM019 Lymphosarcoma 46 1.899
192
MYL069 Myeloma, Multiple 76 1.885
193
HMR002 Hemarthrosis 43 1.881
194
P MTC003 Metachromatic Leukodystrophy 71 1.881
195
THR068 Thrombophilia Due to Protein C Deficiency, Autosomal Recessive 38 1.835
196
CRD132 Cardiac Conduction Defect 59 1.830
197
IMP005 Impotence 52 1.827
198
P PRK039 Parkinsonism 55 1.826
199
HYP005 Hypokalemia 55 1.818
200
ULC004 Ulcerative Colitis 74 1.809
201
ANX010 Anxiety 70 1.806
202
THR067 Thrombophilia Due to Protein C Deficiency, Autosomal Dominant 29 1.792
203
P SZR006 Seizure Disorder 69 1.787
204
DFF031 Diffuse Alveolar Hemorrhage 31 1.783
205
LPT014 Leptin Deficiency or Dysfunction 77 1.777
206
LMB062 Limb Ischemia 55 1.771
207
P RSP003 Respiratory Failure 73 1.771
208
P OVR082 Overgrowth Syndrome 41 1.767
209
DYS073 Dysphagia 53 1.767
210
DRM006 Dermatitis 61 1.759
211
c GRV008 Graves Disease 1 54 1.747
212
c HPT073 Hepatitis C Virus 70 1.725
213
P CND004 Candidiasis 57 1.721
214
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 1.715
215
HRT011 Heart Septal Defect 49 1.698
216
LVD003 Livedoid Vasculitis 37 1.679
217
GST092 Gastroesophageal Reflux 59 1.673
218
c HPT003 Hepatitis a 63 1.673
219
c PRS130 Prostate Cancer, Hereditary, 8 32 1.671
220
c PRS136 Prostate Cancer, Hereditary, 6 33 1.671
221
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 1.671
222
SYN036 Syncope 44 1.662
223
HMG002 Hemoglobinuria 50 1.657
224
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 1.647
225
P HYP086 Hypothyroidism 68 1.617
226
BDD001 Budd-Chiari Syndrome 62 1.616
227
c EHL080 Ehlers-Danlos Syndrome, Musculocontractural Type, 1 53 1.615
228
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 1.586
229
ORL005 Oral Candidiasis 55 1.574
230
MYT019 May-Thurner Syndrome 27 1.568
231
P BRC006 Brachydactyly 52 1.567
232
CRN017 Coronary Thrombosis 46 1.562
233
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 1.559
234
c PRM038 Primary Agammaglobulinemia 47 1.559
235
CLT003 Colitis 63 1.557
236
SYS003 Systolic Heart Failure 49 1.553
237
ART035 Arterial Calcification of Infancy 58 1.551
238
P DRR001 Diarrhea 55 1.550
239
P HNT016 Huntington Disease 73 1.549
240
c HYP836 Hypercholesterolemia, Familial, 1 73 1.548
242
BNR002 Bone Resorption Disease 47 1.543
243
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 1.540
244
GT001 Gout 63 1.536
245
c ACT068 Acute Cystitis 60 1.530
246
P ANT001 Anterolateral Myocardial Infarction 34 1.530
247
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 1.523
248
CTS005 Catastrophic Antiphospholipid Syndrome 43 1.520
249
CRH005 Crohn's Colitis 53 1.520
250
AYM001 Ayme-Gripp Syndrome 57 1.503
251
OST159 Osteogenic Sarcoma 66 1.503
252
CLL003 Cellulitis 53 1.503
253
P INT070 Intestinal Obstruction 57 1.495
254
P EPL164 Epilepsy 70 1.482
255
P URT039 Urticaria 57 1.477
256
c CHN028 Chondrodysplasia Punctata 1, X-Linked Recessive 32 1.477
257
c SCN007 Secondary Hyperparathyroidism 50 1.474
258
P SYS005 Systemic Scleroderma 73 1.469
259
HRP004 Herpes Zoster 60 1.469
260
SKN016 Skin Disease 63 1.464
261
P ART021 Arteriosclerosis 53 1.459
262
HMR039 Hemorrhage, Intracerebral 57 1.442
263
P HYP098 Hypereosinophilic Syndrome 66 1.436
264
P OPT006 Optic Nerve Disease 57 1.435
265
c PSR028 Psoriasis 7 42 1.427
266
c PSR023 Psoriasis 1 52 1.427
267
EPT021 Epithelial Recurrent Erosion Dystrophy 45 1.427
268
c PSR017 Psoriasis 2 53 1.427
269
AMD002 Amed Syndrome, Digenic 36 1.427
270
c PSR018 Psoriasis 13 40 1.427
271
c PSR032 Psoriasis 11 47 1.427
272
CHR682 Chronic Bilirubin Encephalopathy 37 1.427
273
c OVR114 Ovarian Cancer 1 60 1.420
274
RTN017 Retinal Detachment 60 1.419
275
RNL114 Renal Cell Carcinoma, Nonpapillary 79 1.407
276
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 47 1.403
277
BNG077 Benign Idiopathic Neonatal Seizures 23 1.386
278
P SLP006 Sleep Apnea 69 1.382
279
P RTN022 Retinal Vein Occlusion 54 1.379
280
P BLD134 Bladder Cancer 79 1.372
281
INF034 Infective Endocarditis 53 1.371
282
c ACQ014 Acquired Hemophilia 45 1.366
283
P VNS003 Venous Insufficiency 54 1.356
284
CRN006 Coronary Aneurysm 41 1.352
285
RYN005 Raynaud Phenomenon 45 1.352
286
P VNT002 Ventricular Septal Defect 58 1.349
287
P PRG092 Pregnancy Loss, Recurrent 1 42 1.340
288
INT076 Intracranial Sinus Thrombosis 33 1.340
289
P PRP034 Purpura Fulminans 41 1.331
290
SCH018 Schizencephaly 52 1.329
291
ANG054 Angina Pectoris 65 1.321
292
P CRC039 Coarctation of Aorta 46 1.312
293
MXL016 Maxillonasal Dysplasia, Binder Type 32 1.312
294
MCR013 Microphthalmia 59 1.312
295
P RRH023 Rare Hereditary Hemochromatosis 52 1.312
297
PRS045 Prostatic Hypertrophy 53 1.305
298
LNG099 Lung Disease 62 1.296
299
P BCL017 B-Cell Lymphoma 57 1.295
300
CHN065 Choanal Atresia, Posterior 48 1.294
301
P GST053 Gastric Cancer 82 1.291
302
PLG002 Plague 58 1.291
303
P PRS038 Personality Disorder 65 1.291
304
c HMP029 Hemophilia a 69 1.289
305
PRS129 Prostatic Hyperplasia, Benign 48 1.284
306
PRS021 Prostatic Adenoma 43 1.284
307
P PRP019 Peripheral Nervous System Disease 57 1.282
308
PRP007 Priapism 46 1.282
309
c BRN108 Branchiootic Syndrome 1 63 1.273
310
HYP025 Hyperphosphatemia 47 1.273
311
SPL006 Splenic Infarction 37 1.273
312
P AMY004 Amyloidosis 69 1.273
313
P GST044 Gastritis 55 1.270
314
P NRP001 Neuropathy 59 1.263
315
APH002 Aphasia 55 1.255
316
OST062 Osteoarthritis with Mild Chondrodysplasia 46 1.254
317
c SYS043 Systemic Lupus Erythematosus 1 38 1.254
318
HYP555 Hypertriglyceridemia, Transient Infantile 39 1.254
319
END040 Endogenous Depression 54 1.254
320
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 40 1.254
321
NRT001 Neurotic Disorder 56 1.254
322
HYP081 Hypolipoproteinemia 49 1.254
323
HMT002 Hematologic Cancer 61 1.254
324
VSL002 Visual Epilepsy 39 1.254
325
RPD005 Rapidly Involuting Congenital Hemangioma 48 1.248
326
P BRS047 Breast Cancer 97 1.241
327
P CMP008 Compartment Syndrome 49 1.234
328
SBC016 Subacute Delirium 42 1.233
329
P HYP061 Hypertrophic Cardiomyopathy 68 1.230
330
P HML002 Hemolytic Anemia 62 1.217
331
INT067 Interstitial Nephritis 46 1.213
332
P ALP008 Alopecia 53 1.213
333
CRT013 Carotid Stenosis 51 1.211
334
PNG002 Pain Agnosia 51 1.209
335
PRP016 Paraplegia 52 1.209
336
CNN005 Connective Tissue Disease 66 1.206
337
FSC004 Fasciitis 49 1.203
338
TXC005 Toxic Shock Syndrome 61 1.200
339
GST023 Gastric Ulcer 52 1.199
340
CHN071 Chondrodysplasia Punctata, Autosomal Dominant 19 1.199
341
HYP056 Hypoglycemia 65 1.193
342
DRG024 Drug Allergy 40 1.192
343
HMC014 Homocysteinemia 52 1.187
344
CNT016 Central Retinal Vein Occlusion 53 1.184
345
P GRV001 Graves' Disease 54 1.184
346
P DDN001 Duodenal Ulcer 52 1.175
347
c XLN227 X-Linked Chondrodysplasia Punctata 1 35 1.167
348
P PTN014 Patent Ductus Arteriosus 1 59 1.167
349
ANT009 Antithrombin Iii Deficiency 59 1.167
350
BCK006 Back Pain 43 1.166
351
THR123 Thrombotic Microangiopathy 40 1.166
352
ESP002 Esophageal Varix 51 1.151
353
P SKN015 Skin Carcinoma 71 1.147
354
ILS001 Ileus 49 1.147
355
VSC002 Vascular Dementia 59 1.147
356
P DRM010 Dermatomyositis 61 1.138
357
ART008 Arteriosclerosis Obliterans 40 1.128
358
CNS004 Constipation 56 1.128
359
DSS032 Disease by Infectious Agent 55 1.125
360
P MGR003 Migraine with Aura 51 1.118
361
CVD001 Covid-19 59 1.103
362
SNG003 Single Ventricular Heart 30 1.102
363
DXT001 Dextrocardia 54 1.101
364
STS002 Situs Inversus 44 1.101
365
CYT002 Cytokine Deficiency 43 1.097
366
P VNW001 Von Willebrand's Disease 64 1.095
367
c MJR022 Major Affective Disorder 8 37 1.090
368
c MJR024 Major Affective Disorder 9 40 1.090
369
P BPL003 Bipolar Disorder 56 1.090
370
ALC007 Alcohol Dependence 65 1.087
371
ART074 Aortic Dissection 53 1.087
372
VTM009 Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 1 32 1.086
373
SPN186 Spinal Cord Injury 60 1.079
374
NNB001 Nonbacterial Thrombotic Endocarditis 36 1.075
375
P LNG064 Lung Cancer Susceptibility 3 69 1.075
376
PHR003 Pharyngitis 57 1.075
377
NCR007 Necrotizing Fasciitis 48 1.075
378
P PNM007 Pneumonia 64 1.061
379
P DRM053 Dermatitis, Atopic 65 1.059
380
URM002 Uremia 47 1.054
381
ATR055 Atrial Septal Aneurysm 23 1.051
382
MRF001 Marfan Syndrome 76 1.046
383
THR004 Thrombocytosis 52 1.046
384
HYP066 Hyperglycemia 60 1.046
385
P INF038 Influenza 68 1.045
386
SND002 Sneddon Syndrome 48 1.043
387
ATM095 Autoimmune Disease 61 1.038
388
P CLS010 Cluster Headache 42 1.038
389
HPT019 Hepatic Encephalopathy 59 1.037
390
ADN018 Adenoma 58 1.037
391
HPT004 Hepatic Coma 43 1.037
392
FCT007 Factor Vii Deficiency 64 1.028
393
P MCR384 Microcephaly, Epilepsy, and Diabetes Syndrome 1 41 1.025
394
IRN002 Iron Metabolism Disease 56 1.023
395
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 1.019
396
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 1.019
397
CRN030 Coronary Stenosis 50 1.019
398
DFF005 Diffuse Large B-Cell Lymphoma 55 1.010
399
P HMN010 Hemangioma 61 1.010
400
c BCT007 Bacterial Meningitis 55 1.010
401
ANG011 Angiodysplasia 42 1.010
402
P SBS003 Substance Abuse 54 1.010
403
c THR082 Thrombophilia Due to Activated Protein C Resistance 58 1.007
404
P BND020 Bone Disease 60 1.000
405
STT001 Status Epilepticus 58 1.000
406
P CHR345 Chronic Pain 50 1.000
407
CYS001 Cystic Fibrosis 77 0.990
408
P SML001 Small Cell Carcinoma 52 0.990
409
MCR011 Microinvasive Gastric Cancer 41 0.990
410
INF118 Inflammatory Myopathy with Abundant Macrophages 27 0.990
411
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.989
412
PRT129 Prothrombin Deficiency, Congenital 50 0.986
413
c DWL002 Dowling-Degos Disease 1 58 0.980
414
EXP004 Exophthalmos 50 0.980
415
CRD137 Cardiogenic Shock 56 0.980
416
c DRM054 Dermatitis, Atopic, 2 47 0.973
417
P MLT020 Multiple Sclerosis 79 0.972
418
RCK004 Rickets 64 0.970
419
c CHR708 Chronic Urticaria 42 0.963
420
c CRB051 Cerebral Cavernous Malformation, Familial 41 0.953
421
CHR431 Chronic Venous Insufficiency 48 0.952
422
PCT003 Pectus Excavatum 43 0.948
423
SMN007 Seminoma 42 0.948
424
P TRM003 Tremor 50 0.948
425
P ATR010 Atrial Heart Septal Defect 58 0.945
426
ADP007 Adie Pupil 40 0.943
427
HNM002 Hinman Syndrome 29 0.943
428
P TTR001 Tetralogy of Fallot 69 0.940
429
P MMB011 Membranous Nephropathy 50 0.937
430
CHL067 Cholecystitis 59 0.937
431
PLM001 Pulmonary Tuberculosis 69 0.937
432
P ADN016 Adenocarcinoma 63 0.937
433
ACT003 Acute Kidney Tubular Necrosis 46 0.937
434
P PYL005 Pyelonephritis 56 0.925
435
ANR004 Anuria 44 0.925
436
AMN003 Amnestic Disorder 53 0.925
437
BRN026 Branch Retinal Artery Occlusion 41 0.925
438
P OVR046 Ovarian Cyst 43 0.925
439
APP008 Appendicitis 62 0.925
440
P RTN014 Retinal Artery Occlusion 46 0.925
441
ATM021 Autoimmune Inner Ear Disease 36 0.923
442
OLG003 Oligohydramnios 50 0.922
443
OST003 Osteonecrosis 60 0.915
445
VTM010 Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 2 23 0.913
446
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.913
447
QDR001 Quadriplegia 49 0.913
448
INT002 Intermittent Claudication 61 0.907
449
CHR710 Chronic Spontaneous Urticaria 45 0.900
450
c ATM011 Autoimmune Hepatitis 62 0.900
451
c ACQ017 Acquired Von Willebrand Syndrome 48 0.900
452
P RHB003 Rhabdomyosarcoma 66 0.900
453
HYP074 Hypersensitivity Vasculitis 53 0.900
454
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 0.887
455
P FBR017 Fibrosarcoma 55 0.887
456
CHR073 Choreatic Disease 53 0.887
457
P HYP055 Hypoplastic Left Heart Syndrome 65 0.887
458
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 41 0.887
459
P CRV039 Cervicitis 52 0.886
460
VRL011 Viral Infectious Disease 60 0.886
461
c MCR133 Microvascular Complications of Diabetes 4 41 0.883
462
c MCR113 Microvascular Complications of Diabetes 3 52 0.883
463
c MCR130 Microvascular Complications of Diabetes 6 41 0.883
464
c MCR120 Microvascular Complications of Diabetes 7 47 0.883
465
P ENC018 Encephalopathy 62 0.874
466
P CRP001 Carpal Tunnel Syndrome 65 0.873
467
c GLL024 Gallbladder Disease 1 53 0.873
468
c MYC058 Myocardial Infarction 2 23 0.873
469
HYD002 Hydronephrosis 58 0.873
470
c ALM001 Al Amyloidosis 54 0.873
471
P ESS003 Essential Thrombocythemia 68 0.866
472
ATS010 Autosomal Recessive Disease 42 0.860
473
CLF001 Cleft Lip 54 0.860
474
c HYD064 Hydrocephalus, Congenital, 1 51 0.858
475
c MLG069 Malignant Hypertension 46 0.858
476
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.848
477
P PLY018 Polycythemia 56 0.848
478
ING001 Inguinal Hernia 59 0.839
479
P SCK002 Sick Sinus Syndrome 55 0.839
480
TRC022 Tricuspid Valve Insufficiency 46 0.839
481
PLC008 Placenta Disease 48 0.839
482
P OVR042 Ovarian Cancer 88 0.837
483
P NJM001 Nijmegen Breakage Syndrome 75 0.837
484
ALN001 Aland Island Eye Disease 55 0.837
485
ANG049 Angioedema Induced by Ace Inhibitors 38 0.837
486
SLT014 Salt and Pepper Developmental Regression Syndrome 43 0.837
487
c FNC043 Fanconi Anemia, Complementation Group E 62 0.837
488
HYP458 Hyper Ige Syndrome 60 0.837
489
PRT012 Prothrombin Deficiency 50 0.837
490
AMR003 Amaurosis Fugax 32 0.830
491
GST050 Gastrointestinal System Disease 55 0.830
492
HMS001 Hemosiderosis 48 0.825
493
P CRY006 Cryofibrinogenemia 26 0.825
494
FCL014 Focal Epilepsy 53 0.820
495
CRT016 Carotid Artery Disease 52 0.820
496
SPN051 Spondylitis 51 0.820
497
INF009 Inflammatory Spondylopathy 30 0.820
498
PRT036 Peritonitis 65 0.820
499
c ACT134 Acute Liver Failure 57 0.820
500
CMP010 Complex Regional Pain Syndrome 59 0.817
501
NRL016 Neural Tube Defects 80 0.816
502
P CHL066 Cholangitis 51 0.810
503
c ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.807
504
GST045 Gastroenteritis 58 0.807
505
P ART023 Arthropathy 59 0.807
506
RDC002 Radiculopathy 51 0.807
507
CNT061 Conotruncal Heart Malformations 66 0.800
508
c INF071 Inflammatory Bowel Disease 1 65 0.800
509
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.800
510
PRT124 Portal Vein, Cavernous Transformation of 11 0.800
511
P KHL003 Kohlschutter-Tonz Syndrome 57 0.800
512
CRN241 Corneal Dystrophy, Congenital Stromal 49 0.800
513
SPR126 Superior Semicircular Canal Dehiscence 41 0.800
514
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.800
515
IDP011 Idiopathic Interstitial Pneumonia 59 0.800
516
ACT029 Acute Interstitial Pneumonia 49 0.800
517
c HMG029 Hemoglobin Se Disease 41 0.800
518
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.790
519
P THR005 Thrombotic Thrombocytopenic Purpura 64 0.790
520
P ICH004 Ichthyosis 56 0.789
521
P KLL001 Kallmann Syndrome 65 0.789
522
TRC097 Tracheomalacia 43 0.787
523
CHN075 Chondrodysplasia Punctata, Brachytelephalangic, Autosomal 28 0.787
524
c LKM063 Leukemia, Chronic Myeloid 70 0.787
525
INT003 Intracranial Hypotension 36 0.787
526
CRN036 Craniopharyngioma 63 0.787
527
ISC015 Ischemic Colitis 43 0.779
528
c HMP004 Hemophilia B 68 0.779
529
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.768
530
PLY001 Polycythemia Vera 69 0.768
531
BRN024 Bronchitis 67 0.768
532
THR035 Thrombasthenia 48 0.763
533
P PSD087 Pseudoxanthoma Elasticum 66 0.757
534
P CLR023 Colorectal Cancer 100 0.757
535
P ANG015 Angioedema 56 0.757
536
PRM236 Primary Biliary Cholangitis 62 0.757
537
GRM010 Germ Cells Tumors 33 0.757
538
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.753
539
SPN041 Spinal Cord Disease 54 0.753
540
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.745
541
PPL021 Papilledema 49 0.745
542
MXD032 Mixed Germ Cell Tumor 24 0.745
543
CRB132 Cerebral Sinovenous Thrombosis 31 0.745
544
LDW001 Ludwig's Angina 24 0.736
545
CGN006 Cogan Syndrome 49 0.733
546
P KDN017 Kidney Cancer 60 0.733
547
GTR002 Goiter 52 0.733
548
P NTR004 Neutropenia 62 0.728
549
TRC062 Tricuspid Atresia 54 0.720
550
END057 Endometrial Cancer 76 0.720
551
OST017 Osteomyelitis 63 0.720
552
CLR109 Colorectal Adenocarcinoma 50 0.720
553
c FML021 Familial Hypercholesterolemia 71 0.720
554
P ADL010 Adult Respiratory Distress Syndrome 70 0.720
555
c JVN010 Juvenile Rheumatoid Arthritis 52 0.720
556
GLM045 Glioma 62 0.720
557
FNT004 Fainting 29 0.720
558
GLL048 Glial Tumor 51 0.720
559
MYL031 Myeloproliferative Neoplasm 66 0.717
560
IMM167 Immune Deficiency Disease 76 0.707
561
PRP009 Peripartum Cardiomyopathy 54 0.707
562
P CNJ013 Conjunctivitis 66 0.707
563
FMR003 Femoral Neuropathy 37 0.707
564
CMM005 Common Cold 55 0.707
565
DNG003 Dengue Disease 65 0.707
566
HMZ003 Homozygous Familial Hypercholesterolemia 60 0.707
567
HYP266 Hypoxia 56 0.707
568
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 0.707
569
ACT119 Acute Promyelocytic Leukemia 62 0.693
570
ERY003 Erythema Multiforme 56 0.693
571
ACT149 Acetaminophen Metabolism 37 0.693
572
CYC008 Cyclic Vomiting Syndrome 46 0.693
573
c MCR115 Microvascular Complications of Diabetes 5 65 0.693
574
c VNT028 Ventricular Septal Defect 1 28 0.693
575
SVR097 Severe Cutaneous Adverse Reaction 68 0.693
576
P DNG005 Dengue Virus 55 0.693
577
PRT010 Parathyroid Carcinoma 68 0.693
578
PRS064 Persistent Vegetative State 33 0.693
579
P PLY014 Polycystic Kidney Disease 71 0.693
580
SVR004 Severe Combined Immunodeficiency 70 0.693
581
INF013 Inferior Myocardial Infarction 33 0.693
582
c VRL010 Viral Hepatitis 52 0.693
583
BRC012 Brucellosis 66 0.693
584
P END044 Endometriosis 62 0.693
585
P MCR010 Microcephaly 59 0.693
586
PNN001 Panniculitis 52 0.693
587
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 0.693
588
CNT028 Central Retinal Artery Occlusion 42 0.693
589
SPT004 Septic Arthritis 58 0.693
590
c BCT006 Bacterial Conjunctivitis 43 0.693
591
DDN006 Duodenitis 49 0.693
592
P PLY017 Polyarteritis Nodosa 59 0.693
593
ERY066 Erythema Multiforme Major 29 0.693
594
P ESP024 Esophagitis 60 0.682
595
TND005 Tendinitis 53 0.678
596
P MYS005 Myositis 55 0.678
597
HYP029 Hyperthyroxinemia 32 0.678
598
HYP014 Hyperuricemia 51 0.678
599
P EYD002 Eye Disease 57 0.678
600
MMB001 Membranoproliferative Glomerulonephritis 56 0.678
601
OST011 Osteomalacia 52 0.678
602
P RNL015 Renal Hypertension 45 0.678
603
MNC006 Monoclonal Gammopathy of Uncertain Significance 47 0.678
604
PLM186 Pulmonary Arterial Hypertension Associated with Portal Hypertension 25 0.678
605
c BRC078 Brachydactyly, Type A1 56 0.667
606
LPD016 Lipoid Proteinosis of Urbach and Wiethe 50 0.667
607
LYM004 Lymphoid Interstitial Pneumonia 49 0.667
608
NRL018 Neural Tube Defects, Folate-Sensitive 46 0.667
609
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.667
610
LWC002 Lowe Oculocerebrorenal Syndrome 68 0.667
611
DND001 Dandy-Walker Syndrome 48 0.667
612
c DPH024 Diaphragmatic Hernia, Congenital 63 0.667
613
PHL006 Phelan-Mcdermid Syndrome 61 0.667
614
ENT001 Enterocele 42 0.667
615
CRT017 Cartilage Disease 52 0.667
616
c INH020 Inherited Metabolic Disorder 47 0.667
617
DXT002 Dextrocardia with Situs Inversus 43 0.667
618
DFF027 Diffuse Lymphatic Malformation 19 0.667
619
P HYP265 Hypotonia 42 0.667
620
ADN002 Adenoiditis 36 0.662
621
P NNN008 Noonan Syndrome 1 76 0.662
622
P SRC025 Sarcoidosis 1 70 0.662
623
HYP114 Hypertensive Nephropathy 35 0.662
624
c TYP008 Type 1 Diabetes Mellitus 77 0.662
625
MLD018 Mild Cognitive Impairment 48 0.662
626
DPH001 Diphtheria 59 0.662
627
DRG002 Drug-Induced Hepatitis 42 0.662
628
BRS051 Breast Disease 58 0.662
629
P AXN001 Axonal Neuropathy 33 0.662
630
BRK012 Broken Heart Syndrome 42 0.662
631
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.662
632
CTN019 Cutaneous Polyarteritis Nodosa 27 0.662
633
GRW007 Growth Hormone Deficiency 47 0.662
634
PNM013 Pneumococcal Meningitis 43 0.662
635
PRS115 Prosthetic Joint Infection 42 0.662
636
c PSD047 Pseudo-Turner Syndrome 52 0.662
637
ACT162 Acute Sensory Ataxic Neuropathy 24 0.662
638
DNT046 Dental Abscess 32 0.646
639
c ACT004 Acute Diarrhea 40 0.646
640
MNN043 Meningioma, Familial 79 0.646
641
CHL065 Cholangiocarcinoma 57 0.646
642
P LKM071 Leukemia, Chronic Lymphocytic 74 0.646
643
P RCT021 Rectum Cancer 54 0.646
644
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.646
645
NPH009 Nephrolithiasis 54 0.646
646
FRZ001 Frozen Shoulder 54 0.646
647
VGN017 Vaginal Cancer 58 0.646
648
SCR001 Secretory Meningioma 40 0.646
649
OST004 Osteitis Fibrosa 38 0.646
650
BNN003 Bone Inflammation Disease 47 0.646
651
INT079 Intrahepatic Cholangiocarcinoma 51 0.646
652
BRS064 Bursitis 51 0.646
653
P OPN001 Open-Angle Glaucoma 55 0.646
654
TTN003 Tetanus 64 0.646
655
P UVT001 Uveitis 57 0.646
656
INT395 Intracranial Meningioma 47 0.646
657
HRD160 Hereditary Combined Deficiency of Vitamin K-Dependent Clotting Factors 25 0.646
658
P LCT001 Lactic Acidosis 50 0.646
659
GST040 Gastric Adenocarcinoma 66 0.646
660
FCT013 Factor V Leiden Thrombophilia 20 0.646
661
ALL014 Allergic Encephalomyelitis 34 0.646
662
MDR006 Moderate and Severe Traumatic Brain Injury 27 0.646
663
CHG001 Chagas Disease 65 0.642
664
OTT002 Otitis Media 70 0.627
665
c GLC092 Glaucoma, Primary Open Angle 60 0.627
666
P LRY029 Laryngomalacia 47 0.627
667
P STR020 Strabismus 56 0.627
668
c SPR086 Spermatogenic Failure 3 47 0.627
669
BRK010 Burkitt Lymphoma 65 0.627
670
CLR108 Colorectal Adenoma 63 0.627
671
PST028 Post-Traumatic Stress Disorder 58 0.627
672
MYL001 Myelitis 49 0.627
673
CHL068 Cholestasis 61 0.627
674
P HYP730 Hypogonadotropic Hypogonadism 57 0.627
675
LCH001 Leech Infestation 37 0.627
676
P NRM002 Normal Pressure Hydrocephalus 49 0.627
677
PLR007 Pleural Empyema 50 0.627
678
MDD011 Mood Disorder 61 0.627
679
P BRS044 Breast Adenocarcinoma 58 0.627
680
LCK001 Locked-in Syndrome 44 0.627
681
PLR008 Pleurisy 49 0.627
682
MYS001 Myositis Ossificans 44 0.627
683
P ATR005 Atrophic Gastritis 50 0.627
684
MCH006 Mechanical Strabismus 40 0.627
685
PCT001 Pectus Carinatum 33 0.627
686
c PRT132 Protoporphyria, Erythropoietic, 1 61 0.614
687
CRS005 Crest Syndrome 36 0.607
688
PFF001 Pfeiffer Syndrome 77 0.607
689
TND004 Tendinopathy 45 0.607
690
P DVL012 Developmental Dysplasia of the Hip 1 45 0.607
691
HYP781 Hypoascorbemia 52 0.607
692
CRV035 Cervical Cancer 72 0.607
693
c SYS047 Systemic Lupus Erythematosus 7 13 0.607
694
P SPN052 Spondyloarthropathy 54 0.607
695
VLV011 Vulvovaginal Candidiasis 49 0.607
696
FCT008 Factitious Disorder 34 0.607
697
SPN011 Spongiotic Dermatitis 31 0.607
698
GST037 Gastroparesis 52 0.607
699
SYN007 Synovitis 54 0.607
700
GNG013 Gingivitis 59 0.607
701
PLC002 Plica Syndrome 35 0.607
702
NPH010 Nephrosclerosis 50 0.607
703
KHN001 Kuhnt-Junius Degeneration 48 0.607
704
CRS001 Crescentic Glomerulonephritis 42 0.607
705
FTN001 Fat Necrosis of Breast 20 0.607
706
TRC016 Tracheal Calcification 25 0.607
707
HPT022 Hepatoblastoma 54 0.607
708
c ATS347 Autosomal Dominant Polycystic Kidney Disease 64 0.607
709
PLY012 Polyhydramnios 46 0.607
710
NNN007 Non-Involuting Congenital Hemangioma 40 0.607
711
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 0.594
712
HMP005 Hemiplegia 53 0.592
713
STT041 Stuttering 52 0.584
714
MNC002 Munchausen by Proxy 29 0.584
715
P CLC063 Celiac Disease 1 65 0.584
716
FBR011 Fibrodysplasia Ossificans Progressiva 67 0.584
717
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.584
718
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.584
719
P TMP003 Temporal Arteritis 68 0.584
720
KLP010 Klippel-Trenaunay-Weber Syndrome 59 0.584
721
FCT006 Factor V Deficiency 55 0.584
722
ALV001 Alveolar Periostitis 34 0.584
723
P PLY011 Polycystic Ovary Syndrome 57 0.584
724
SHW001 Shwartzman Phenomenon 36 0.584
725
LGP001 Lagophthalmos 30 0.584
726
RSC001 Rosacea 55 0.584
727
ALL006 Allergic Asthma 55 0.584
728
P MYT002 Myotonic Dystrophy 51 0.584
729
ORP003 Oropharynx Cancer 54 0.584
730
HVY002 Heavy Metal Poisoning 22 0.584
731
RRC033 Rare Coagulation Disorder 12 0.584
732
SPN340 Spontaneous Intracranial Hypotension 28 0.584
733
c PNC132 Pancreatic Cancer 5 22 0.556
734
MYL005 Myelofibrosis 70 0.556
735
INT303 Intracranial Hypertension, Idiopathic 56 0.556
736
P ACT028 Acute Closed-Angle Glaucoma 32 0.556
737
P LMY004 Leiomyosarcoma 62 0.556
738
P ACN011 Acne 55 0.556
739
RTR007 Retroperitoneal Leiomyosarcoma 27 0.556
740
P PRR002 Pure Red-Cell Aplasia 46 0.556
741
PCD001 Pica Disease 38 0.556
742
BCK003 Background Diabetic Retinopathy 46 0.556
743
P MYL006 Myeloid Leukemia 60 0.556
744
GNT005 Giant Hemangioma 27 0.556
745
P MYC008 Myocarditis 59 0.556
746
THN005 Thunderclap Headache 16 0.556
747
NRR001 Neuroretinitis 42 0.532
748
ENT004 Enthesopathy 51 0.532
749
P MNN013 Meningitis 65 0.532
750
P PRN026 Porencephaly 54 0.520
751
BHC003 Behcet Syndrome 70 0.520
752
DFN341 Deafness, Unilateral 24 0.520
753
CRP030 Corpus Callosum, Agenesis of, with Facial Anomalies and Cerebellar Ataxia 37 0.520
754
BRG013 Buerger Disease 56 0.520
755
P GLN011 Glanzmann Thrombasthenia 1 66 0.520
756
INT051 Intussusception 53 0.520
757
KDN001 Kidney Cortex Necrosis 31 0.520
758
BRN008 Brain Compression 25 0.520
759
FBR047 Fibromyalgia 57 0.520
760
RYS001 Reye Syndrome 49 0.520
761
c ESS001 Essential Tremor 56 0.520
762
ERD001 Erdheim-Chester Disease 53 0.520
763
GNG012 Gingival Overgrowth 49 0.520
764
PLX004 Plexopathy 29 0.520
765
GSG001 Gas Gangrene 52 0.520
766
CHR177 Chromophobe Renal Cell Carcinoma 54 0.520
767
TNS014 Tenosynovitis 45 0.520
768
c CNG216 Congenital Hydrocephalus 50 0.520
769
P CPL006 Capillary Hemangioma 53 0.505
770
RTN023 Retinitis 45 0.505
771
P HRP006 Herpes Simplex 65 0.505
772
P MYP004 Myopathy 67 0.488
773
P ART005 Arteriovenous Malformation 64 0.473
774
P SCH015 Schizophrenia 74 0.469
775
P MJR007 Major Affective Disorder 1 42 0.469
776
P STR092 Striatal Degeneration, Autosomal Dominant 2 44 0.469
777
CYT005 Cytomegalovirus Retinitis 50 0.469
778
DYS165 Dysfibrinogenemia, Congenital 52 0.469
779
DFF003 Diffuse Scleroderma 41 0.469
780
PLS011 Plasmacytoma 56 0.469
781
CNN003 Conn's Syndrome 77 0.469
782
PLS009 Plasma Cell Neoplasm 64 0.469
783
CNT015 Central Sleep Apnea 46 0.469
784
P PRD008 Periodontitis 63 0.469
785
c PRC016 Pre-Eclampsia 64 0.465
786
OSS012 Osseous Heteroplasia, Progressive 61 0.434
787
MYX004 Myxedema 43 0.434
788
RFL001 Reflex Sympathetic Dystrophy 51 0.434
789
KWS001 Kwashiorkor 44 0.434
790
P END047 Endophthalmitis 53 0.434
791
MRK001 Merkel Cell Carcinoma 64 0.434
792
P NRV006 Nervous System Cancer 47 0.434
793
P MGR001 Migraine Without Aura 48 0.434
794
ALG001 Algoneurodystrophy 37 0.434
795
PLN007 Plantar Fasciitis 37 0.434
796
TRC023 Trichinosis 53 0.434
797
ATY005 Atypical Teratoid Rhabdoid Tumor 69 0.417
798
INT078 Intracranial Thrombosis 50 0.414
799
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.396
800
RSP027 Respiratory Papillomatosis, Juvenile Recurrent, Congenital 47 0.382
801
BHR001 Behr Syndrome 51 0.382
802
P ATS364 Autism 72 0.382
803
CPL013 Capillary Malformations, Congenital 53 0.382
804
RYN001 Raynaud Disease 49 0.382
805
KND001 Kindler Syndrome 63 0.382
806
c MJR008 Major Affective Disorder 2 34 0.382
807
c PNS012 Paine Syndrome 60 0.382
808
c MJR006 Major Affective Disorder 5 32 0.382
809
c MJR023 Major Affective Disorder 7 33 0.382
810
CHP002 Chops Syndrome 47 0.382
811
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 0.382
812
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 54 0.382
813
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.382
814
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.382
815
APN008 Apnea, Obstructive Sleep 66 0.382
816
BRD001 Brody Myopathy 55 0.382
817
ORT008 Orotic Aciduria 56 0.382
818
c MJR004 Major Affective Disorder 4 28 0.382
819
c MJR003 Major Affective Disorder 6 32 0.382
820
BNM001 Bone Marrow Cancer 45 0.382
821
P MLN008 Melanoma 75 0.382
822
c LCL006 Localized Scleroderma 64 0.382
823
SKN019 Skin Melanoma 70 0.382
824
RTC005 Reticulosarcoma 47 0.382
825
MNN020 Meningococcal Infection 44 0.382
826
CHL079 Children's Interstitial Lung Disease 25 0.382
827
NSS002 Neisseria Meningitidis Infection 46 0.382
828
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.382
829
INT066 Interstitial Lung Disease 60 0.376
830
c PRG042 Progressive Familial Heart Block, Type Ia 65 0.366
831
HLC007 Helicobacter Pylori Infection 67 0.366
832
RTN020 Retinal Vascular Disease 45 0.366
833
PSY004 Psychotic Disorder 66 0.366
834
SGT001 Sagittal Sinus Thrombosis 36 0.356
835
P ECL001 Eclampsia 52 0.345
836
SYS071 Systemic Autoimmune Disease 35 0.345
837
SRT004 Serotonin Syndrome 54 0.345
838
GLM044 Glomerular Disease 34 0.345
840
P MYC084 Mycobacterium Tuberculosis 1 68 0.323
841
RHM001 Rheumatic Fever 59 0.323
842
CLP006 Clopidogrel Resistance 44 0.323
843
P INF037 Inflammatory Bowel Disease 53 0.311
844
ASP026 Asplenia, Isolated Congenital 43 0.311
845
P OBS001 Obstructive Jaundice 49 0.311
846
CYN002 Cyanosis, Transient Neonatal 43 0.299
847
ESP021 Esophageal Cancer 84 0.299
848
P CYS018 Cystitis 58 0.299
849
PNC129 Pancreatic Adenocarcinoma 64 0.299
850
TNS005 Tonsillitis 57 0.299
851
CHR603 Chronic Enteropathy Associated with Slco2a1 Gene 25 0.299
852
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.286
853
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.286
854
ASP030 Aspirin Resistance 41 0.286
855
FCL012 Facial Paralysis 49 0.286
856
RGH001 Right Bundle Branch Block 47 0.286
857
P HMR005 Hemorrhoid 49 0.286
858
c RRH015 Rare Hemorrhagic Disorder 22 0.286
859
PST092 Posttransplant Acute Limbic Encephalitis 29 0.286
860
ATR057 Atrioventricular Block 54 0.273
861
ANT078 Antipyrine Metabolism 24 0.273
862
CLF027 Cleft Palate, Isolated 64 0.273
863
PNM008 Pneumothorax 54 0.273
864
MSN001 Mesangial Proliferative Glomerulonephritis 44 0.273
865
BLD131 Bladder Urothelial Carcinoma 59 0.273
866
LMY002 Leiomyoma 51 0.273
867
TLN003 Telangiectasis 51 0.273
868
FTT001 Fatty Liver Disease 61 0.273
869
SPL018 Splenomegaly 47 0.273
870
RST023 Resting Heart Rate, Variation in 40 0.259
871
PRC013 Pericarditis 53 0.259
872
INT075 Intracranial Hypertension 52 0.259
873
c AVS006 Avascular Necrosis of Femoral Head, Primary, 1 42 0.244
874
CHR001 Churg-Strauss Syndrome 61 0.244
875
RTN021 Retinal Vascular Occlusion 45 0.244
876
P SYP003 Syphilis 59 0.244
877
P PRL003 Proliferative Glomerulonephritis 43 0.244
878
CRT015 Carotid Artery Occlusion 45 0.244
879
MSC007 Muscle Hypertrophy 64 0.228
880
WLF001 Wolff-Parkinson-White Syndrome 63 0.228
881
P ORT004 Orthostatic Intolerance 61 0.228
882
LMR001 Lemierre's Syndrome 39 0.228
883
HYP080 Hypogonadism 49 0.228
884
BLR008 Bilirubin Metabolic Disorder 57 0.228
885
P LNG028 Long Qt Syndrome 63 0.228
886
ART017 Aortic Disease 49 0.228
887
ECT004 Ecthyma 26 0.228
888
SVR001 Severe Acute Respiratory Syndrome 68 0.228
889
MYF001 Myofibroma 42 0.228
890
P HRD008 Hereditary Hemorrhagic Telangiectasia 64 0.228
891
URL001 Urolithiasis 45 0.228
892
LFT001 Left Bundle Branch Hemiblock 47 0.228
893
ACQ007 Acquired Immunodeficiency Syndrome 58 0.228
894
DBL004 Double Discordia 20 0.228
895
UNV002 Univentricular Heart 26 0.228
896
PRS063 Paresthesia 39 0.228
897
SPS057 Spasticity 43 0.228
898
P SCL018 Scoliosis 57 0.211
899
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.211
900
LYM133 Lymphoma, Hodgkin, Classic 69 0.211
901
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.211
902
ADN027 Adenomyosis 59 0.211
903
PRT019 Protein-Losing Enteropathy 44 0.211
904
P LKM002 Leukemia 65 0.211
905
TRN018 Transitional Cell Carcinoma 56 0.211
906
BCT022 Bacterial Infectious Disease 55 0.211
907
GST071 Gastrointestinal Carcinoma 46 0.211
908
AMN001 Amenorrhea 53 0.211
909
IRN001 Iron Deficiency Anemia 58 0.211
910
GST049 Gastrointestinal System Cancer 49 0.211
911
END021 Endomyocardial Fibrosis 56 0.211
912
BLT003 Blue Toe Syndrome 25 0.211
913
c SVR005 Severe Pre-Eclampsia 49 0.211
914
CRT008 Carotid Artery Dissection 29 0.211
915
PTH003 Pathologic Nystagmus 52 0.211
916
ALL012 Allergic Angiitis 24 0.211
917
CRB086 Cerebral Aneurysms 40 0.211
918
P APL001 Aplastic Anemia 72 0.193
919
c ANM038 Anemia, Autoimmune Hemolytic 63 0.193
920
FCT003 Factor X Deficiency 54 0.193
921
P PLY006 Polydactyly 58 0.193
922
P MCR129 Microvascular Complications of Diabetes 1 67 0.193
923
P NSP012 Nasopharyngeal Carcinoma 60 0.193
924
c MCR112 Microvascular Complications of Diabetes 2 42 0.193
925
HLX001 Helix Syndrome 47 0.193
926
KPS004 Kaposi Sarcoma 76 0.193
927
P LKM062 Leukemia, Acute Lymphoblastic 69 0.193
929
GRN037 Granulomatosis with Polyangiitis 66 0.193
930
P DXT004 Dextro-Looped Transposition of the Great Arteries 58 0.193
931
HMR023 Hemorrhagic Cystitis 43 0.193
932
INT030 Intracranial Aneurysm 55 0.193
933
P RNV001 Renovascular Hypertension 48 0.193
934
P HRN001 Horner's Syndrome 45 0.193
935
BSL004 Basilar Artery Occlusion 33 0.193
936
BRN004 Brain Edema 54 0.193
937
P PLM025 Pulmonary Venoocclusive Disease 44 0.193
938
LYM027 Lymphopenia 56 0.193
939
INF021 Infant Gynecomastia 30 0.193
940
CRY004 Cryoglobulinemia 47 0.193
941
SBC003 Subacute Bacterial Endocarditis 33 0.193
942
SPN035 Spindle Cell Sarcoma 51 0.193
943
GYN001 Gynecomastia 48 0.193
944
SRC014 Sarcoma 64 0.193
945
DNG002 Dengue Hemorrhagic Fever 59 0.193
946
APC001 Apical Myocardial Infarction 16 0.193
947
ACT084 Acute Stress Disorder 53 0.193
948
SPN027 Spinal Stenosis 58 0.193
949
HTR003 Heterotaxy 43 0.193
950
P HMC002 Homocystinuria 52 0.193
951
SCT002 Scotoma 42 0.193
952
PLC007 Placental Abruption 47 0.193
953
INT059 Internal Hemorrhoid 36 0.193
954
P THY032 Thyroiditis 56 0.193