Search results for Heparin

2744 hits were found for Heparin

# Family MCID Name MIFTS Score
1
HPR003 Heparin-Induced Thrombocytopenia 47 67.606
2
HPR006 Heparin Cofactor Ii Deficiency 37 52.337
3
P THR014 Thrombocytopenia 66 34.647
4
c THR092 Thrombophilia Due to Thrombin Defect 74 29.301
5
THR024 Thrombosis 56 23.732
6
PLM033 Pulmonary Embolism 58 21.833
7
INT007 Intermediate Coronary Syndrome 53 15.095
8
c ACT075 Acute Myocardial Infarction 55 12.045
9
P MYC007 Myocardial Infarction 69 11.852
10
DSS009 Disseminated Intravascular Coagulation 56 11.081
11
P THR015 Thrombophilia 51 10.904
12
ISC004 Ischemia 61 10.859
13
P ANT006 Antiphospholipid Syndrome 55 10.037
14
LPP008 Lipoprotein Quantitative Trait Locus 65 10.035
15
ANG054 Angina Pectoris 65 9.369
16
c ACT071 Acute Kidney Failure 60 8.866
17
END086 End Stage Renal Disease 54 8.741
18
ART140 Arteries, Anomalies of 52 8.519
19
THR016 Thrombophlebitis 50 8.437
20
P KDN018 Kidney Disease 72 8.358
21
ANT009 Antithrombin Iii Deficiency 59 8.351
22
P VSC007 Vascular Disease 62 8.187
23
CVD001 Covid-19 58 8.126
24
P ATR011 Atrial Fibrillation 66 7.994
25
c PRC016 Pre-Eclampsia 64 7.648
26
TXC005 Toxic Shock Syndrome 62 7.494
27
48X005 48,xyyy 39 7.489
28
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 37 7.463
29
STR067 Stroke, Ischemic 79 7.326
30
P RSP003 Respiratory Failure 74 6.812
31
c CHR684 Chronic Kidney Disease 74 6.812
32
P ADL010 Adult Respiratory Distress Syndrome 71 6.779
33
PRP027 Peripheral Vascular Disease 71 6.705
34
ANR040 Aneurysm 60 6.551
35
ALL029 Allergic Disease 61 6.498
36
P CRN300 Coronary Heart Disease 1 73 6.449
37
SVR001 Severe Acute Respiratory Syndrome 68 6.246
38
ART016 Aortic Aneurysm 69 6.227
39
LMB062 Limb Ischemia 55 6.160
40
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 6.155
41
CRD137 Cardiogenic Shock 56 6.128
42
c ACT027 Acute Pancreatitis 60 5.958
43
PRP030 Purpura 54 5.908
44
P PNC044 Pancreatitis 61 5.894
45
P PST095 Post-Thrombotic Syndrome 50 5.755
46
PLC008 Placenta Disease 49 5.607
47
P ECL001 Eclampsia 52 5.601
48
P HRT032 Heart Disease 84 5.583
49
CRB039 Cerebrovascular Disease 65 5.560
50
P PNM007 Pneumonia 64 5.507
51
SPN186 Spinal Cord Injury 61 5.461
52
HPT046 Hepatic Veno-Occlusive Disease 55 5.373
53
c HYP724 Hyperlipoproteinemia, Type Iii 66 5.340
54
CRN017 Coronary Thrombosis 46 5.321
55
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 5.293
56
LVR012 Liver Cirrhosis 62 5.267
57
P PLM037 Pulmonary Hypertension 69 5.215
58
c HYP836 Hypercholesterolemia, Familial, 1 73 5.146
59
P INT143 Interstitial Cystitis 59 5.044
60
P CYS018 Cystitis 59 5.027
61
P GLM007 Glomerulonephritis 59 4.958
62
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 4.886
63
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 4.801
64
P INF032 Infertility 60 4.772
65
P OST002 Osteoporosis 77 4.756
66
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 4.756
67
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 4.756
68
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 4.747
69
P PRG092 Pregnancy Loss, Recurrent 1 42 4.711
70
PRT036 Peritonitis 65 4.706
71
PRT018 Portal Vein Thrombosis 50 4.686
72
CLT003 Colitis 63 4.577
73
P PNC035 Pancreatic Cancer 86 4.548
74
P HYP750 Hypertriglyceridemia, Familial 62 4.457
75
CYT002 Cytokine Deficiency 43 4.445
76
P ART021 Arteriosclerosis 53 4.429
77
ANT039 Antisynthetase Syndrome 55 4.359
78
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 4.358
79
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 4.358
80
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 4.358
81
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 4.358
82
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 4.358
83
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 4.358
84
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 4.358
85
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 4.358
86
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 4.358
87
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 4.294
88
RPD005 Rapidly Involuting Congenital Hemangioma 48 4.272
89
P CRD119 Cardiac Arrest 68 4.251
90
ATH013 Atherosclerosis Susceptibility 63 4.246
91
BRN071 Brain Injury 50 4.230
92
TRM010 Traumatic Brain Injury 50 4.210
93
VTM033 Vitamin K Deficiency Bleeding 50 4.204
94
P LNG032 Lung Cancer 98 4.195
95
P SCK005 Sickle Cell Disease 56 4.174
96
ULC004 Ulcerative Colitis 74 4.167
97
47X002 47,xyy 48 4.113
98
P NPH012 Nephrotic Syndrome 62 4.099
99
CRB086 Cerebral Aneurysms 40 4.094
100
PNG002 Pain Agnosia 51 4.078
101
P BLD124 Bleeding Disorder, Platelet-Type, 11 68 4.016
102
HLX001 Helix Syndrome 47 4.001
103
c SVR005 Severe Pre-Eclampsia 50 3.977
104
P CTR002 Cataract 59 3.968
105
P CRD246 Cardiovascular System Disease 55 3.965
106
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 3.960
107
P VTR007 Vitreoretinopathy 45 3.960
108
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 3.946
109
MYL069 Myeloma, Multiple 77 3.946
110
P LVR013 Liver Disease 68 3.896
111
EXT007 Extracutaneous Mastocytoma 38 3.874
112
MST004 Mast Cell Neoplasm 41 3.874
113
INT030 Intracranial Aneurysm 55 3.863
114
TRN015 Transient Cerebral Ischemia 62 3.862
115
DFC004 Deficiency Anemia 74 3.782
116
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 3.753
117
CNG034 Congestive Heart Failure 69 3.745
118
BCT022 Bacterial Infectious Disease 56 3.741
119
THR004 Thrombocytosis 52 3.726
120
PLM129 Pulmonary Disease, Chronic Obstructive 74 3.692
121
P CLR023 Colorectal Cancer 100 3.689
122
P OVR042 Ovarian Cancer 88 3.647
123
PRP080 Peripheral Artery Disease 54 3.639
124
RHB024 Rhabdomyosarcoma 2 65 3.632
125
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 3.619
126
c TYP008 Type 1 Diabetes Mellitus 77 3.595
127
BNR002 Bone Resorption Disease 47 3.569
128
c PNS012 Paine Syndrome 60 3.568
129
c LKM061 Leukemia, Acute Myeloid 83 3.553
130
PRT013 Portal Hypertension 59 3.553
131
P END033 Endocarditis 58 3.552
132
PRT011 Protein C Deficiency 47 3.544
133
INT002 Intermittent Claudication 61 3.530
134
CLN015 Colon Adenocarcinoma 64 3.487
135
P AMY004 Amyloidosis 69 3.466
136
HRT011 Heart Septal Defect 49 3.459
137
P LKM002 Leukemia 66 3.439
138
P VSC011 Vasculitis 61 3.432
139
LPT014 Leptin Deficiency or Dysfunction 77 3.425
140
P GST053 Gastric Cancer 82 3.373
141
VRC005 Varicose Veins 59 3.370
142
c SYS001 Systemic Lupus Erythematosus 86 3.368
143
P URN019 Urinary Tract Infection 49 3.365
144
OST012 Osteoarthritis 77 3.360
145
PRT251 Proteinuria, Chronic Benign 58 3.356
146
RTN017 Retinal Detachment 60 3.351
147
P LPS004 Lupus Erythematosus 61 3.329
148
P CMP008 Compartment Syndrome 50 3.328
149
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 3.321
150
P HRP006 Herpes Simplex 65 3.280
151
c HYP595 Hypertension, Essential 84 3.276
152
PRT014 Protein S Deficiency 46 3.269
153
HDN002 Head Injury 44 3.253
154
GLM045 Glioma 62 3.249
155
DWN001 Down Syndrome 70 3.235
156
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 3.220
157
P CNJ013 Conjunctivitis 66 3.210
158
P ADN016 Adenocarcinoma 63 3.209
159
P ESS003 Essential Thrombocythemia 68 3.208
160
BLD051 Blood Coagulation Disease 53 3.197
161
PLM010 Pulmonary Edema 54 3.191
162
GLL048 Glial Tumor 52 3.184
163
INT078 Intracranial Thrombosis 50 3.184
164
c ACT073 Acute Leukemia 59 3.116
165
PLC007 Placental Abruption 47 3.115
166
PRP016 Paraplegia 52 3.095
167
FCT001 Factor Viii Deficiency 62 3.094
168
P NRB001 Neuroblastoma 66 3.082
169
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 3.082
170
P VNS003 Venous Insufficiency 54 3.072
171
P HPT023 Hepatocellular Carcinoma 95 3.066
172
ATM095 Autoimmune Disease 61 3.032
173
GLB002 Glioblastoma 67 3.016
174
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 3.005
175
c PRM038 Primary Agammaglobulinemia 47 3.004
176
P UVT001 Uveitis 57 2.997
177
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 2.993
179
ACT058 Active Peptic Ulcer Disease 55 2.979
180
INT010 Intracranial Embolism 48 2.962
181
KRT002 Keratomalacia 54 2.955
182
LNG099 Lung Disease 62 2.955
183
VCC001 Vaccinia 49 2.954
184
PLC005 Placental Insufficiency 56 2.948
185
P ATR010 Atrial Heart Septal Defect 58 2.946
186
c FML001 Familial Atrial Fibrillation 65 2.941
187
c MCR133 Microvascular Complications of Diabetes 4 41 2.940
188
c MCR113 Microvascular Complications of Diabetes 3 52 2.940
189
c MCR130 Microvascular Complications of Diabetes 6 41 2.940
190
c MCR120 Microvascular Complications of Diabetes 7 47 2.940
191
c ACT068 Acute Cystitis 61 2.931
192
P LKM062 Leukemia, Acute Lymphoblastic 69 2.928
193
CRH001 Crohn's Disease 80 2.916
194
P TRN020 Turner Syndrome 67 2.913
195
INF034 Infective Endocarditis 53 2.870
196
P HYP098 Hypereosinophilic Syndrome 66 2.868
197
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 2.868
198
STM007 Stomatitis 52 2.857
199
SRC014 Sarcoma 64 2.857
200
SPN035 Spindle Cell Sarcoma 51 2.857
201
DPH001 Diphtheria 59 2.844
203
CHR682 Chronic Bilirubin Encephalopathy 37 2.835
204
P PLY018 Polycythemia 56 2.820
205
c EPS039 Episodic Pain Syndrome, Familial, 1 42 2.817
206
P BRS047 Breast Cancer 97 2.816
207
LPD008 Lipid Metabolism Disorder 61 2.813
208
P MTR003 Mitral Valve Stenosis 53 2.812
209
P PRS040 Prostate Cancer 95 2.786
210
BRN026 Branch Retinal Artery Occlusion 41 2.784
211
P HYP120 Hypoaldosteronism 33 2.778
212
P HML001 Hemolytic-Uremic Syndrome 52 2.776
213
P URT039 Urticaria 57 2.775
214
OST159 Osteogenic Sarcoma 66 2.772
215
P ANG015 Angioedema 56 2.755
216
MYL005 Myelofibrosis 70 2.742
217
CTS005 Catastrophic Antiphospholipid Syndrome 43 2.733
218
ART074 Aortic Dissection 53 2.731
219
P DBT009 Diabetes Mellitus 67 2.726
220
HYP060 Hyperinsulinism 53 2.725
221
ADL002 Adult Syndrome 69 2.714
222
SCK003 Sickle Cell Anemia 74 2.710
223
BDD001 Budd-Chiari Syndrome 62 2.702
224
P MYL006 Myeloid Leukemia 60 2.699
225
P HMP007 Hemophilia 52 2.690
226
P THR005 Thrombotic Thrombocytopenic Purpura 64 2.677
227
P PRP034 Purpura Fulminans 41 2.670
228
P GLM040 Glioma Susceptibility 1 70 2.663
229
CRD001 Cardiac Tamponade 44 2.658
230
URM002 Uremia 47 2.634
231
CNN005 Connective Tissue Disease 66 2.624
232
P HMN010 Hemangioma 61 2.614
233
P HYP768 Hyperlipoproteinemia, Type I 67 2.612
234
HYP066 Hyperglycemia 60 2.590
235
P MYC008 Myocarditis 59 2.589
236
c HRD002 Hereditary Angioedema 61 2.586
237
AND005 Androgen Insensitivity Syndrome, Mild 21 2.584
238
P RTN014 Retinal Artery Occlusion 47 2.583
239
P ANR048 Aniridia 1 66 2.578
240
c FML021 Familial Hypercholesterolemia 71 2.576
241
P HPT021 Hepatitis 68 2.576
242
LYM019 Lymphosarcoma 46 2.575
243
c THR082 Thrombophilia Due to Activated Protein C Resistance 58 2.574
244
IMM167 Immune Deficiency Disease 77 2.548
245
c VRL005 Viral Pneumonia 52 2.546
246
P RTN022 Retinal Vein Occlusion 54 2.539
247
HYP081 Hypolipoproteinemia 49 2.538
248
P ART005 Arteriovenous Malformation 65 2.534
249
P BCT020 Bacteremia 2 43 2.528
250
DRM006 Dermatitis 62 2.526
251
P PLM036 Pulmonary Fibrosis 65 2.516
252
PTN001 Patent Foramen Ovale 62 2.509
253
c SML038 Small Cell Cancer of the Lung 69 2.508
254
HRT012 Heart Valve Disease 53 2.507
255
HMN044 Human Immunodeficiency Virus Type 1 76 2.506
256
c MCR115 Microvascular Complications of Diabetes 5 65 2.497
257
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 2.497
258
MCS002 Mucositis 55 2.491
259
PLY001 Polycythemia Vera 69 2.489
260
SGT001 Sagittal Sinus Thrombosis 36 2.485
261
PRT019 Protein-Losing Enteropathy 44 2.483
262
LYM005 Lymphocele 31 2.483
263
IRN002 Iron Metabolism Disease 56 2.472
264
ENT004 Enthesopathy 51 2.464
265
RNL114 Renal Cell Carcinoma, Nonpapillary 79 2.456
266
HGH043 High Grade Glioma 46 2.450
267
P HML002 Hemolytic Anemia 62 2.434
268
THR100 Thrombocytopenic Purpura, Autoimmune 60 2.419
269
P MST009 Mastocytosis 64 2.414
270
CHR431 Chronic Venous Insufficiency 48 2.403
271
INT076 Intracranial Sinus Thrombosis 30 2.398
272
ENT011 Enterocolitis 55 2.381
273
P NRP001 Neuropathy 59 2.377
274
c THR037 Thrombocytopenia 2 37 2.375
275
P ART022 Arthritis 70 2.373
276
c ACT134 Acute Liver Failure 57 2.369
277
P EXN002 Exanthem 58 2.360
278
c ART101 Aortic Valve Disease 2 65 2.357
279
HMG002 Hemoglobinuria 50 2.354
280
MTB004 Metabolic Acidosis 48 2.349
281
c HNT011 Huntington Disease-Like 3 33 2.346
282
PRN019 Perinatal Necrotizing Enterocolitis 60 2.341
283
NRR001 Neuroretinitis 42 2.341
284
RTN023 Retinitis 45 2.341
285
P LYM118 Lymphoma 69 2.327
286
P NTR004 Neutropenia 62 2.324
287
c HNT004 Huntington Disease-Like 2 51 2.321
288
P MLN008 Melanoma 75 2.317
289
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 2.295
290
NTR005 Nutritional Deficiency Disease 60 2.293
291
PRT037 Pertussis 49 2.292
292
CRT084 Creatinine Clearance Quantitative Trait Locus 25 2.286
293
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 2.285
294
PRP007 Priapism 46 2.271
295
THR123 Thrombotic Microangiopathy 40 2.265
296
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 2.264
297
OCL069 Ocular Motor Apraxia 57 2.259
298
P MYC084 Mycobacterium Tuberculosis 1 68 2.259
299
P LNG064 Lung Cancer Susceptibility 3 70 2.258
300
P BRS044 Breast Adenocarcinoma 58 2.257
301
P INF037 Inflammatory Bowel Disease 53 2.254
302
INT075 Intracranial Hypertension 52 2.245
303
c ACQ005 Acquired Thrombocytopenia 35 2.244
304
ACT119 Acute Promyelocytic Leukemia 62 2.223
305
BRN028 Brain Cancer 73 2.219
306
P ENC004 Encephalitis 61 2.213
307
MYL031 Myeloproliferative Neoplasm 66 2.213
308
ACT017 Acute Chest Syndrome 50 2.212
309
c ATR087 Atrial Standstill 1 74 2.212
310
P VNW001 Von Willebrand's Disease 64 2.210
311
c DLT002 Dilated Cardiomyopathy 79 2.197
312
CRB004 Cerebral Artery Occlusion 46 2.192
313
HMR039 Hemorrhage, Intracerebral 57 2.166
314
SPN027 Spinal Stenosis 59 2.159
315
BLS001 Blau Syndrome 68 2.148
316
INS024 Insulin-Like Growth Factor I 77 2.145
317
P ANT001 Anterolateral Myocardial Infarction 34 2.145
318
CRN030 Coronary Stenosis 50 2.141
319
HMP001 Hemopericardium 47 2.140
320
CRD223 Cardiac Arrhythmia 63 2.137
321
PRL017 Prolymphocytic Leukemia 47 2.121
322
PRD013 Periodic Fever, Familial, Autosomal Dominant 67 2.121
323
c ACT150 Acute Adrenal Insufficiency 48 2.118
324
PRS045 Prostatic Hypertrophy 52 2.108
325
P FBR017 Fibrosarcoma 55 2.106
326
BWN001 Bowen-Conradi Syndrome 54 2.105
327
CYS001 Cystic Fibrosis 77 2.095
328
P PRK057 Parkinson Disease, Late-Onset 79 2.093
329
NWB001 Newborn Respiratory Distress Syndrome 56 2.089
330
DBT008 Diabetic Angiopathy 47 2.070
331
PST011 Pustulosis of Palm and Sole 52 2.060
332
P PSR002 Psoriasis 63 2.060
333
CRT013 Carotid Stenosis 51 2.055
334
SNG003 Single Ventricular Heart 30 2.044
335
c HMP004 Hemophilia B 68 2.029
336
CRT004 Carotid Artery Thrombosis 39 2.020
337
AFB002 Afibrinogenemia, Congenital 64 2.014
338
P MNN013 Meningitis 65 2.014
339
P CNR004 Cone-Rod Dystrophy 2 75 2.009
340
OST062 Osteoarthritis with Mild Chondrodysplasia 47 2.009
341
CLC001 Calciphylaxis 50 2.007
342
ATX019 Ataxia with Vitamin E Deficiency 44 2.001
343
P LCH002 Lichen Planus 55 2.000
344
PRS129 Prostatic Hyperplasia, Benign 48 1.996
345
P AST005 Asthma 76 1.996
346
P PLY011 Polycystic Ovary Syndrome 57 1.992
347
AGN016 Aging 54 1.968
348
SFT003 Soft Tissue Sarcoma 57 1.957
349
CYN002 Cyanosis, Transient Neonatal 43 1.954
350
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 1.953
351
PNC129 Pancreatic Adenocarcinoma 65 1.953
352
MST024 Mastocytosis, Cutaneous 66 1.951
353
HNC001 Henoch-Schoenlein Purpura 56 1.951
354
URL001 Urolithiasis 45 1.947
355
SPL004 Splenic Marginal Zone Lymphoma 50 1.944
356
BLD044 Bladder Disease 48 1.940
357
P PRC012 Pericardial Effusion 50 1.938
358
BRN024 Bronchitis 67 1.935
359
PRT012 Prothrombin Deficiency 48 1.933
360
PRS021 Prostatic Adenoma 43 1.929
361
GST023 Gastric Ulcer 52 1.927
362
BRN004 Brain Edema 54 1.921
363
P INT260 Intracranial Berry Aneurysm 39 1.915
364
ESP021 Esophageal Cancer 84 1.912
365
P FNG006 Feingold Syndrome 1 61 1.909
366
CRB009 Cerebritis 43 1.905
367
HYP056 Hypoglycemia 65 1.901
369
SVR004 Severe Combined Immunodeficiency 71 1.888
370
P ESP024 Esophagitis 60 1.887
371
RYN005 Raynaud Phenomenon 45 1.884
372
P HDC001 Headache 56 1.880
373
P APL001 Aplastic Anemia 73 1.877
374
ESP002 Esophageal Varix 51 1.872
375
HMP005 Hemiplegia 53 1.868
376
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.863
377
DSS032 Disease by Infectious Agent 55 1.857
378
ALL006 Allergic Asthma 56 1.844
379
PPL021 Papilledema 49 1.809
380
FML026 Familial Lipoprotein Lipase Deficiency 52 1.799
381
P TTR001 Tetralogy of Fallot 69 1.799
382
NNB001 Nonbacterial Thrombotic Endocarditis 36 1.796
383
LCH001 Leech Infestation 38 1.793
384
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.784
385
ADR040 Adrenal Gland Pheochromocytoma 45 1.780
386
P PHC003 Pheochromocytoma 70 1.780
387
P SRC025 Sarcoidosis 1 70 1.776
388
SHW001 Shwartzman Phenomenon 36 1.773
389
PRC013 Pericarditis 53 1.770
390
P CHN012 Chondrosarcoma 56 1.767
391
ACT011 Acute Contagious Conjunctivitis 42 1.763
392
AMN003 Amnestic Disorder 54 1.762
393
MTR002 Mitral Valve Insufficiency 51 1.760
394
P INF038 Influenza 68 1.757
395
P ALP008 Alopecia 53 1.755
396
STN005 St Anthony's Fire 18 1.755
397
MNN021 Meningococcemia 34 1.742
398
c MGR028 Migraine with or Without Aura 1 64 1.736
399
CRN027 Corneal Neovascularization 47 1.733
400
ARG004 Argyria 26 1.729
401
LNG031 Lung Benign Neoplasm 51 1.720
402
BCT021 Bacterial Sepsis 43 1.717
403
PRS047 Prostatitis 58 1.716
404
CNT016 Central Retinal Vein Occlusion 54 1.713
405
c MCR112 Microvascular Complications of Diabetes 2 42 1.712
406
P MCR129 Microvascular Complications of Diabetes 1 68 1.712
407
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 1.706
408
ACQ007 Acquired Immunodeficiency Syndrome 58 1.694
409
CHL014 Cholera 62 1.693
410
P PRN023 Prion Disease 60 1.692
411
CHR100 Chronic Ulcer of Skin 57 1.688
412
AGG012 Aggressive Nk-Cell Leukemia 47 1.683
413
SQM006 Squamous Cell Carcinoma 59 1.677
414
P BRN019 Bernard-Soulier Syndrome 61 1.674
415
P PRD008 Periodontitis 64 1.673
416
SYN036 Syncope 44 1.672
417
END057 Endometrial Cancer 71 1.670
418
P HYP076 Hyperthyroidism 53 1.670
419
HYP266 Hypoxia 56 1.667
420
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 1.661
421
P LKM071 Leukemia, Chronic Lymphocytic 74 1.658
422
P PYL005 Pyelonephritis 56 1.655
423
P PRC031 Preeclampsia/eclampsia 1 43 1.653
424
MLR004 Malaria 78 1.647
425
ANX004 Anoxia 40 1.646
426
PLS011 Plasmacytoma 56 1.640
427
c HMP029 Hemophilia a 69 1.639
428
P ENC018 Encephalopathy 62 1.637
429
c LYS019 Loeys-Dietz Syndrome 1 58 1.637
430
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 57 1.637
431
c GLL024 Gallbladder Disease 1 53 1.633
432
HLL004 Hellp Syndrome 53 1.625
433
P HYD006 Hydrocephalus 63 1.625
434
ING001 Inguinal Hernia 59 1.623
435
ADN018 Adenoma 58 1.622
436
PLT015 Platelet Aggregation, Spontaneous 34 1.615
437
PLM001 Pulmonary Tuberculosis 69 1.612
438
c HPT073 Hepatitis C Virus 71 1.611
439
FTT001 Fatty Liver Disease 61 1.611
440
ART002 Arts Syndrome 66 1.603
441
HMR002 Hemarthrosis 44 1.600
442
CHR466 Chronic Thromboembolic Pulmonary Hypertension 47 1.598
443
TRT001 Teratocarcinoma 41 1.596
444
P GST044 Gastritis 55 1.595
445
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 37 1.594
446
CLC006 Calcinosis 47 1.593
447
FML035 Familial Hyperlipidemia 55 1.585
448
URN022 Urinary Tract Infections, Recurrent 27 1.580
449
c HPT016 Hepatitis B 62 1.575
450
FMR003 Femoral Neuropathy 35 1.574
451
P ANP001 Anaplastic Large Cell Lymphoma 61 1.574
452
SKN016 Skin Disease 62 1.572
453
P ESP035 Esophagitis, Eosinophilic, 1 57 1.571
454
LYM027 Lymphopenia 56 1.570
455
THR035 Thrombasthenia 48 1.570
456
P NSP012 Nasopharyngeal Carcinoma 60 1.569
457
NPH091 Nephrolithiasis, Calcium Oxalate 61 1.564
458
ART008 Arteriosclerosis Obliterans 40 1.563
459
XNT003 Xanthomatosis 48 1.556
460
CHL123 Chlamydia 58 1.553
461
LVD003 Livedoid Vasculitis 35 1.549
462
P DNG005 Dengue Virus 55 1.547
463
CRT072 Creutzfeldt-Jakob Disease 67 1.543
464
CNT047 Contact Dermatitis 57 1.540
465
c HPT003 Hepatitis a 63 1.538
466
INT276 Interatrial Communication 50 1.538
467
P BCL017 B-Cell Lymphoma 57 1.536
468
MDD018 Middle East Respiratory Syndrome 44 1.534
469
c BCT007 Bacterial Meningitis 55 1.533
470
c ACT076 Acute Myocarditis 47 1.532
471
PLM134 Pulmonary Fibrosis, Idiopathic 76 1.528
472
ANR007 Anorexia Nervosa 59 1.526
473
OST017 Osteomyelitis 63 1.525
474
ASP030 Aspirin Resistance 40 1.525
475
SPR126 Superior Semicircular Canal Dehiscence 41 1.523
476
c HMG029 Hemoglobin Se Disease 41 1.523
477
PTT004 Pituitary Apoplexy 47 1.522
478
TTN003 Tetanus 64 1.521
479
ADN027 Adenomyosis 59 1.520
480
P BND020 Bone Disease 60 1.518
481
IMM236 Immune-Mediated Thrombotic Thrombocytopenic Purpura 23 1.514
482
SPL006 Splenic Infarction 37 1.512
483
BLD053 Blood Platelet Disease 51 1.510
484
c TYP009 Type 2 Diabetes Mellitus 92 1.504
485
c VRL010 Viral Hepatitis 52 1.503
486
P OVR082 Overgrowth Syndrome 42 1.502
487
SCR011 Scrapie 39 1.499
488
APH002 Aphasia 55 1.498
489
P CHR345 Chronic Pain 50 1.497
490
c ACQ014 Acquired Hemophilia 45 1.497
491
EXR010 Exercise-Induced Bronchoconstriction 34 1.494
492
P KDN017 Kidney Cancer 60 1.485
494
c BRN108 Branchiootic Syndrome 1 63 1.484
495
RHM001 Rheumatic Fever 59 1.484
496
RCK004 Rickets 65 1.484
497
HYP063 Hypersplenism 52 1.483
498
c PRG042 Progressive Familial Heart Block, Type Ia 65 1.481
499
MSC007 Muscle Hypertrophy 64 1.477
500
KPS004 Kaposi Sarcoma 76 1.477
501
ORL015 Oral Squamous Cell Carcinoma 43 1.472
502
DRG024 Drug Allergy 40 1.472
503
P RHN004 Rhinitis 57 1.467
504
P RHB003 Rhabdomyosarcoma 66 1.464
505
P VNT002 Ventricular Septal Defect 58 1.460
506
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 41 1.460
507
VGN023 Vaginitis 56 1.459
508
THR017 Thoracoabdominal Syndrome 40 1.455
509
P ALZ034 Alzheimer Disease 87 1.451
510
HYP005 Hypokalemia 55 1.447
511
HMC014 Homocysteinemia 52 1.446
512
KWS002 Kawasaki Disease 65 1.445
513
PRP009 Peripartum Cardiomyopathy 54 1.440
514
P PRL003 Proliferative Glomerulonephritis 43 1.438
515
c ALM001 Al Amyloidosis 54 1.437
516
GNT005 Giant Hemangioma 27 1.435
517
ESN005 Eosinophilic Gastroenteritis 55 1.432
518
PNM008 Pneumothorax 54 1.430
519
P BLD134 Bladder Cancer 79 1.429
520
EMB004 Embryonal Carcinoma 55 1.425
521
P KLZ004 Kala-Azar 1 41 1.414
522
LSH001 Leishmaniasis 63 1.414
523
SMT001 Somatization Disorder 50 1.411
524
GLM044 Glomerular Disease 34 1.411
525
IGG001 Iga Glomerulonephritis 50 1.408
526
P SHR001 Short Bowel Syndrome 53 1.408
527
SBC016 Subacute Delirium 42 1.408
528
MTH009 Mouth Disease 57 1.406
529
FCT003 Factor X Deficiency 54 1.404
530
c THR048 Thrombocytopenia 4 28 1.404
531
VRS002 Virus-Associated Trichodysplasia Spinulosa 30 1.399
532
GSG001 Gas Gangrene 52 1.396
533
CRT016 Carotid Artery Disease 52 1.396
534
HYP043 Hyperandrogenism 47 1.396
535
c MCP043 Mucopolysaccharidosis, Type Iiia 61 1.394
536
c MYC058 Myocardial Infarction 2 24 1.384
537
MYT019 May-Thurner Syndrome 25 1.372
538
TRN018 Transitional Cell Carcinoma 56 1.371
539
c THR102 Thrombocytopenia 5 29 1.369
540
ETV001 Etv6 Thrombocytopenia and Predisposition to Leukemia 31 1.369
541
IMP005 Impotence 52 1.367
542
HMN014 Human Immunodeficiency Virus Infectious Disease 54 1.367
543
SBC003 Subacute Bacterial Endocarditis 33 1.366
544
CRT015 Carotid Artery Occlusion 45 1.361
545
CHL068 Cholestasis 61 1.357
546
C1N001 C1 Inhibitor Deficiency 43 1.356
547
c ANG068 Angioedema, Hereditary, Type I 57 1.356
548
P RBL001 Rubella 58 1.356
549
CHC001 Chickenpox 56 1.356
550
c MCL046 Mucolipidosis Iii Alpha/beta 61 1.355
551
LPT006 Leptin Receptor Deficiency 50 1.355
552
DSS010 Dissociative Disorder 39 1.355
553
c XNT010 Xanthinuria, Type I 52 1.355
554
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 40 1.355
555
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 1.352
556
P SZR006 Seizure Disorder 69 1.352
557
P HMR003 Hemorrhagic Disease 59 1.351
558
HMP009 Haemophilus Influenzae 41 1.351
559
P ALC033 Alcohol Use Disorder 67 1.345
560
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 33 1.344
561
P HYP069 Hyperparathyroidism 62 1.340
562
FCT004 Factor Xii Deficiency 54 1.336
563
c PLM164 Pulmonary Hypertension, Primary, 1 80 1.329
564
GST033 Gestational Diabetes 61 1.329
565
P ACT092 Acth-Independent Macronodular Adrenal Hyperplasia 56 1.326
566
INT053 Intracranial Vasospasm 36 1.326
567
c DPH024 Diaphragmatic Hernia, Congenital 64 1.324
568
MNN043 Meningioma, Familial 79 1.323
569
P LMY004 Leiomyosarcoma 62 1.323
570
CHL070 Cholesterol Embolism 39 1.323
571
P HYP086 Hypothyroidism 69 1.323
572
P SNS001 Sensorineural Hearing Loss 59 1.318
573
P THL005 Thalassemia 56 1.318
574
SPT004 Septic Arthritis 58 1.312
575
P MST002 Mast-Cell Leukemia 50 1.311
576
INT395 Intracranial Meningioma 48 1.309
577
SCR001 Secretory Meningioma 40 1.309
578
LYM002 Lymphoplasmacyte-Rich Meningioma 35 1.309
579
P MYS003 Myasthenia Gravis 68 1.307
580
VRL011 Viral Infectious Disease 60 1.304
581
P MSC005 Muscular Dystrophy 66 1.301
582
OTT002 Otitis Media 71 1.296
583
c SCL052 Scleroderma, Familial Progressive 60 1.296
584
GNT019 Giant Cell Myocarditis 29 1.292
585
CLL003 Cellulitis 53 1.290
586
CVR002 Cavernous Sinus Thrombosis 34 1.286
587
P MMB011 Membranous Nephropathy 50 1.284
588
P SYS005 Systemic Scleroderma 73 1.284
589
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.281
590
LGN005 Ligneous Conjunctivitis 30 1.276
591
P VND001 Vein Disease 42 1.274
592
P PTT006 Pituitary Adenoma 55 1.270
593
INT323 Intraocular Pressure Quantitative Trait Locus 63 1.269
594
ATR057 Atrioventricular Block 54 1.269
595
THR013 Thoracic Outlet Syndrome 46 1.268
596
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.265
597
TRN012 Transient Global Amnesia 38 1.255
598
BLR008 Bilirubin Metabolic Disorder 57 1.253
599
RTN020 Retinal Vascular Disease 45 1.253
600
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 38 1.252
601
CLN045 Colonic Benign Neoplasm 48 1.252
602
CRC021 Carcinosarcoma 62 1.246
603
CHL065 Cholangiocarcinoma 58 1.246
604
INT079 Intrahepatic Cholangiocarcinoma 51 1.246
605
ERY004 Erysipelas 47 1.246
606
HMN047 Human Cytomegalovirus Infection 59 1.243
607
NSS002 Neisseria Meningitidis Infection 47 1.240
608
RSP007 Respiratory Distress Syndrome, Infant 40 1.237
609
MYL009 Myelodysplastic Syndrome 67 1.237
610
P DRM053 Dermatitis, Atopic 65 1.234
611
ALL003 Allergic Rhinitis 66 1.234
612
c PRG043 Progressive Familial Heart Block, Type Ib 54 1.231
613
ANR004 Anuria 44 1.231
614
RGH001 Right Bundle Branch Block 47 1.231
615
P PMP001 Pemphigus 55 1.228
616
HMZ003 Homozygous Familial Hypercholesterolemia 60 1.220
617
LMY002 Leiomyoma 51 1.220
618
c PCH010 Pachyonychia Congenita 3 43 1.219
619
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 1.219
620
ACT113 Acute Myeloblastic Leukemia with Maturation 46 1.216
621
P GRF003 Graft-Versus-Host Disease 71 1.214
622
CHR074 Choriocarcinoma 46 1.214
623
RNL065 Renal Cell Carcinoma, Papillary, 1 79 1.212
624
MLG169 Malignant Astrocytoma 57 1.208
625
P RPD001 Rapidly Progressive Glomerulonephritis 43 1.205
626
URN010 Urinary Tract Obstruction 55 1.205
627
ALC007 Alcohol Dependence 65 1.191
628
ORL011 Oral Cancer 60 1.191
629
c THR071 Thrombocytopenia 1 48 1.190
630
P PTN014 Patent Ductus Arteriosus 1 59 1.190
631
c WLM013 Wilms Tumor 1 65 1.189
632
JPN002 Japanese Encephalitis 61 1.184
633
HRD104 Hereditary Multiple Osteochondromas 43 1.183
634
SDD008 Sudden Sensorineural Hearing Loss 41 1.182
635
PLS009 Plasma Cell Neoplasm 64 1.181
636
CHL067 Cholecystitis 59 1.178
637
P HMR005 Hemorrhoid 49 1.175
638
P HYP055 Hypoplastic Left Heart Syndrome 65 1.175
639
SYS004 Systemic Mastocytosis 62 1.172
640
APP008 Appendicitis 62 1.168
641
HYP080 Hypogonadism 49 1.167
642
ACT056 Acute Cor Pulmonale 37 1.167
643
CRH005 Crohn's Colitis 53 1.167
644
PLC009 Placenta Praevia 39 1.167
645
EXF001 Exfoliation Syndrome 56 1.163
646
VSC002 Vascular Dementia 59 1.163
647
INF013 Inferior Myocardial Infarction 33 1.159
648
P RCT021 Rectum Cancer 54 1.159
649
c PRM093 Premature Ovarian Failure 7 47 1.157
650
PLS007 Plasmodium Falciparum Malaria 52 1.152
651
SPL018 Splenomegaly 47 1.148
652
DBT084 Diabetes Mellitus, Ketosis-Prone 60 1.145
653
OVR029 Ovarian Hyperstimulation Syndrome 63 1.143
654
GT001 Gout 63 1.141
655
GST019 Gastrointestinal Stromal Tumor 78 1.141
656
AYM001 Ayme-Gripp Syndrome 57 1.138
657
P MLG074 Malignant Mesenchymoma 40 1.138
658
P END047 Endophthalmitis 53 1.137
659
ACR008 Acrocallosal Syndrome 70 1.134
660
DNG002 Dengue Hemorrhagic Fever 59 1.133
661
c MLG069 Malignant Hypertension 46 1.132
662
VSC003 Visceral Leishmaniasis 54 1.132
663
P CRN074 Coronary Artery Aneurysm 41 1.132
664
MNN020 Meningococcal Infection 45 1.128
665
PPT005 Peptic Ulcer Disease 58 1.126
666
DYS073 Dysphagia 53 1.125
667
P SYP003 Syphilis 59 1.123
668
FCT002 Factor Xi Deficiency 61 1.123
669
PMP014 Pemphigoid 49 1.123
670
c OVR114 Ovarian Cancer 1 60 1.122
671
LYM017 Lyme Disease 63 1.121
672
ALL014 Allergic Encephalomyelitis 34 1.117
673
P CHR285 Chronic Myelomonocytic Leukemia 59 1.117
674
RFR002 Refractory Hairy Cell Leukemia 34 1.117
675
P MXD050 Mixed Phenotype Acute Leukemia 45 1.117
676
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 1.117
677
KRT019 Keratitis, Hereditary 66 1.114
678
WTR001 Waterhouse-Friderichsen Syndrome 35 1.114
679
END072 Endotheliitis 36 1.113
680
BLL006 Bullous Pemphigoid 61 1.112
681
GLC003 Glucose Intolerance 53 1.110
682
THY029 Thyroid Carcinoma 54 1.109
683
P CRV039 Cervicitis 52 1.107
684
P RNL015 Renal Hypertension 45 1.103
685
HYP736 Hyperheparinemia 12 1.102
686
CLR030 Clear Cell Renal Cell Carcinoma 54 1.097
687
HMN035 Hemangioma-Thrombocytopenia Syndrome 39 1.095
688
YLL002 Yellow Fever 61 1.095
689
CLN006 Colonic Pseudo-Obstruction 30 1.090
690
P HYP730 Hypogonadotropic Hypogonadism 54 1.090
691
P INT068 Intestinal Disease 53 1.088
692
PMP006 Pemphigus Vulgaris, Familial 58 1.088
693
c EXS019 Exostoses, Multiple, Type I 54 1.085
694
ILS001 Ileus 49 1.085
695
P PRK039 Parkinsonism 55 1.084
696
CRB132 Cerebral Sinovenous Thrombosis 29 1.082
697
TRC022 Tricuspid Valve Insufficiency 47 1.079
698
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 1.078
699
DBL002 Double Outlet Right Ventricle 57 1.078
700
NNL006 Non-Alcoholic Steatohepatitis 54 1.074
701
PNM013 Pneumococcal Meningitis 43 1.073
702
GST045 Gastroenteritis 58 1.066
703
P HMP002 Hemophagocytic Lymphohistiocytosis 60 1.065
704
ANC002 Anca-Associated Vasculitis 44 1.065
705
DDN006 Duodenitis 50 1.063
706
ACT181 Acute Motor Axonal Neuropathy 25 1.063
707
P PRS038 Personality Disorder 65 1.056
708
PLR007 Pleural Empyema 51 1.054
709
FSC004 Fasciitis 49 1.054
710
MSN001 Mesangial Proliferative Glomerulonephritis 44 1.053
711
CHR072 Chordoma 57 1.052
712
MXD005 Mixed Connective Tissue Disease 57 1.052
713
P RNV001 Renovascular Hypertension 49 1.051
714
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 1.048
715
BNM001 Bone Marrow Cancer 45 1.048
716
P SCL018 Scoliosis 57 1.046
717
c SCN007 Secondary Hyperparathyroidism 51 1.046
718
c BTT014 Beta-Thalassemia 72 1.045
719
P INT070 Intestinal Obstruction 57 1.045
720
STT001 Status Epilepticus 58 1.040
721
DFF005 Diffuse Large B-Cell Lymphoma 55 1.036
722
P NRV006 Nervous System Cancer 47 1.036
723
c CHR064 Chronic Monocytic Leukemia 36 1.035
725
P ART018 Aortic Valve Insufficiency 52 1.033
726
BRN056 Bronchopulmonary Dysplasia 57 1.033
727
P CLC063 Celiac Disease 1 66 1.026
728
KLD004 Keloid Disorder 39 1.026
729
ASP026 Asplenia, Isolated Congenital 43 1.024
730
GLN010 Glanzmann Thrombasthenia 66 1.022
731
HPT081 Hepatic Infarction 31 1.022
732
P END044 Endometriosis 62 1.009
734
BLT017 Bilateral Massive Adrenal Hemorrhage 16 1.004
735
ACR041 Acromelic Frontonasal Dysostosis 53 1.004
736
FML285 Familial Apolipoprotein C-Ii Deficiency 34 1.004
737
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 63 1.004
738
c CHR708 Chronic Urticaria 42 0.996
739
PNN001 Panniculitis 52 0.996
740
P RHM011 Rheumatoid Arthritis 81 0.996
741
ACT098 Acute Erythroid Leukemia 55 0.996
742
LPM012 Lipomatosis, Multiple 60 0.994
743
P OBS001 Obstructive Jaundice 49 0.988
744
PLS031 Plastic Bronchitis 25 0.988
745
RHM028 Rheumatic Heart Disease 56 0.986
746
SVR097 Severe Cutaneous Adverse Reaction 68 0.984
747
QLT001 Qualitative Platelet Defect 29 0.984
748
LTR004 Lateral Myocardial Infarction 27 0.984
749
STR077 Streptococcal Toxic-Shock Syndrome 34 0.984
750
CLR109 Colorectal Adenocarcinoma 50 0.980
751
MCP033 Mucopolysaccharidoses 44 0.980
752
P DDN001 Duodenal Ulcer 53 0.980
753
CRT008 Carotid Artery Dissection 29 0.980
754
PLY150 Polykaryocytosis Inducer 29 0.974
755
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.974
756
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 52 0.974
757
PRN029 Parainfluenza Virus Type 3 32 0.972
758
c CRB051 Cerebral Cavernous Malformation, Familial 41 0.971
759
HYP458 Hyper Ige Syndrome 60 0.969
760
GLS018 Glass Syndrome 60 0.969
761
KDN007 Kidney Clear Cell Sarcoma 40 0.969
762
CLR017 Clear Cell Sarcoma 44 0.969
763
MXD026 Mixed Glioma 45 0.969
764
CHL079 Children's Interstitial Lung Disease 26 0.969
765
c HNT010 Huntington Disease-Like 1 55 0.964
766
MSL001 Measles 61 0.964
767
GRN017 Granulocytopenia 42 0.964
768
MTL005 Metal Allergy 39 0.961
769
ACT040 Acute Poststreptococcal Glomerulonephritis 35 0.961
770
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 65 0.961
771
WRF003 Warfarin Syndrome 29 0.958
772
PLM022 Pulmonary Valve Insufficiency 45 0.957
773
P EPD016 Epidermolysis Bullosa 53 0.957
774
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.957
775
P PLY019 Polyneuropathy 53 0.955
776
LPT001 Leptospirosis 66 0.955
777
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.951
778
c MSM022 Mismatch Repair Cancer Syndrome 1 69 0.947
779
AMD002 Amed Syndrome, Digenic 37 0.947
780
c EHL080 Ehlers-Danlos Syndrome, Musculocontractural Type, 1 53 0.947
781
c PRS130 Prostate Cancer, Hereditary, 8 32 0.947
782
c PRS136 Prostate Cancer, Hereditary, 6 33 0.947
783
UND007 Undifferentiated Connective Tissue Disease 29 0.947
784
BLD131 Bladder Urothelial Carcinoma 59 0.946
785
c FNC043 Fanconi Anemia, Complementation Group E 62 0.945
786
c SYS043 Systemic Lupus Erythematosus 1 38 0.945
787
c BLD140 Blood Group, I System 47 0.945
788
c ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.942
789
RSP019 Respiratory Distress Syndrome in Premature Infants 52 0.941
790
MCR011 Microinvasive Gastric Cancer 41 0.937
791
TST044 Testicular Torsion 45 0.937
792
P TXP001 Toxoplasmosis 60 0.937
793
P ATR005 Atrophic Gastritis 50 0.937
794
PNC001 Pancytopenia 52 0.935
795
IRN001 Iron Deficiency Anemia 58 0.935
796
c EPD076 Epidermolysis Bullosa Dystrophica, Autosomal Recessive 51 0.933
797
P RCS002 Recessive Dystrophic Epidermolysis Bullosa 62 0.933
798
FBR009 Fibrous Dysplasia 48 0.930
799
c FML346 Familial Adenomatous Polyposis 1 65 0.930
800
CLD011 Cold Urticaria 34 0.930
801
BSL004 Basilar Artery Occlusion 32 0.929
802
c ACT135 Acute Graft Versus Host Disease 51 0.929
803
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.928
804
c DWL002 Dowling-Degos Disease 1 58 0.928
805
SCH014 Schistosomiasis 56 0.928
806
OLG003 Oligohydramnios 51 0.928
807
MCL006 Macular Retinal Edema 56 0.928
808
P DRR001 Diarrhea 55 0.922
809
c MCL013 Mucolipidosis Iv 64 0.918
810
FRN006 Frontotemporal Dementia 68 0.918
811
AML029 Ameloblastoma 46 0.918
812
CRV035 Cervical Cancer 72 0.916
813
ADR016 Adrenal Cortical Carcinoma 61 0.908
814
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.908
815
ADR004 Adrenal Cortical Adenocarcinoma 38 0.908
816
P CHL066 Cholangitis 51 0.908
817
MSC026 Muscular Dystrophy White Matter Spongiosis 13 0.908
818
NCR007 Necrotizing Fasciitis 48 0.908
819
P FCL005 Focal Segmental Glomerulosclerosis 57 0.901
820
CHG001 Chagas Disease 65 0.901
821
MSC157 Muscular Dystrophy, Duchenne Type 79 0.901
822
CHR178 Chromosomal Triplication 34 0.897
823
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.893
824
LPD004 Lipoid Nephrosis 44 0.888
825
TND005 Tendinitis 54 0.886
826
P HRD144 Hereditary Mixed Polyposis Syndrome 54 0.886
827
c CHR098 Chronic Pyelonephritis 34 0.886
828
BRK010 Burkitt Lymphoma 66 0.886
829
P OVR046 Ovarian Cyst 44 0.886
830
BRN002 Bronchiolitis 57 0.886
831
CNT028 Central Retinal Artery Occlusion 42 0.886
832
PRS063 Paresthesia 39 0.886
833
PRT129 Prothrombin Deficiency, Congenital 48 0.883
834
HYP017 Hypophosphatemia 49 0.878
835
PLR008 Pleurisy 49 0.875
836
SLC006 Silicosis 55 0.875
837
P PLM034 Pulmonary Emphysema 58 0.875
838
P HML033 Hemolytic Uremic Syndrome, Atypical 1 68 0.867
839
c HYP272 Hypercholesterolemia, Familial, 3 46 0.866
840
IMM162 Immunoglobulin E Concentration, Serum 28 0.866
841
PLY105 Polycystic Ovary Syndrome 1 39 0.866
842
BCT004 Bacteriuria 48 0.863
843
SNL007 Senile Cataract 40 0.863
844
MRF001 Marfan Syndrome 76 0.863
845
c AMY009 Amyloidosis Aa 47 0.863
846
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.863
847
MNS012 Monostotic Fibrous Dysplasia 19 0.856
848
MST019 Mastoiditis 41 0.854
849
PPL052 Papillomatosis, Confluent and Reticulated 34 0.854
850
NPH009 Nephrolithiasis 54 0.854
851
c DRM040 Dermatitis Herpetiformis, Familial 35 0.850
852
PYD002 Pyoderma 49 0.850
853
P DRM007 Dermatitis Herpetiformis 54 0.850
854
PYD001 Pyoderma Gangrenosum 53 0.850
855
INF118 Inflammatory Myopathy with Abundant Macrophages 27 0.850
856
PRT114 Prothrombin Thrombophilia 25 0.846
857
QDR001 Quadriplegia 49 0.846
858
P NRF002 Neurofibromatosis 60 0.846
859
P JBR020 Joubert Syndrome 1 74 0.844
860
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 63 0.844
861
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 0.844
862
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.844
863
ARM010 Arima Syndrome 56 0.844
864
CYT004 Cytomegalic Inclusion Disease 31 0.844
865
ACY011 Acyl-Coa Dehydrogenase Deficiency 31 0.844
866
P END046 Endometritis 46 0.837
867
P LPR021 Leprosy 3 71 0.837
868
HNS001 Hansen's Disease 32 0.837
869
P PLM064 Pulmonary Sequestration 22 0.837
870
P PLM006 Pulmonary Alveolar Proteinosis 53 0.837
871
P PLY014 Polycystic Kidney Disease 71 0.832
872
GST040 Gastric Adenocarcinoma 66 0.832
873
P GLL018 Gallbladder Cancer 53 0.829
875
INT066 Interstitial Lung Disease 60 0.828
876
GNG013 Gingivitis 59 0.828
877
FCT013 Factor V Leiden Thrombophilia 19 0.828
878
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.828
879
HPT004 Hepatic Coma 43 0.825
880
c ANM038 Anemia, Autoimmune Hemolytic 63 0.819
881
KDN001 Kidney Cortex Necrosis 31 0.819
882
P RTN016 Retinal Degeneration 52 0.819
883
ALP043 Alpha-2-Plasmin Inhibitor Deficiency 44 0.816
884
c THR090 Thrombocythemia 1 50 0.810
885
MCR013 Microphthalmia 60 0.810
886
PTN004 Patent Ductus Venosus 31 0.810
887
HYP457 Hypertrophic Scars 42 0.810
888
URT010 Ureteral Obstruction 45 0.810
889
ART006 Arthus Reaction 40 0.810
890
ADR005 Adrenal Carcinoma 61 0.810
891
c RTN042 Retinitis Pigmentosa 12 42 0.800
892
c VRL012 Viral Meningitis 46 0.800
893
P TRT010 Teratoma 50 0.800
894
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.800
895
P CNT005 Central Nervous System Lymphoma 51 0.799
896
P LCT001 Lactic Acidosis 50 0.795
897
CHR563 Chronic Eosinophilic Leukemia 48 0.793
898
JVN004 Juvenile Myelomonocytic Leukemia 67 0.793
899
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 49 0.793
900
CHR286 Chronic Neutrophilic Leukemia 42 0.793
901
SML014 Small Intestine Leiomyosarcoma 31 0.793
902
LCL004 Localized Osteosarcoma 34 0.793
903
PST046 Post-Transplant Lymphoproliferative Disease 53 0.793
904
INT054 Intraocular Lymphoma 48 0.793
905
c CHR711 Chronic Asthma 41 0.790
906
ANG020 Angiosarcoma 63 0.790
907
P PTS002 Ptosis 52 0.790
908
BRN014 Bronchopneumonia 52 0.790
909
SYN007 Synovitis 54 0.790
910
CRD003 Cardiac Sarcoidosis 44 0.790
911
PLC002 Plica Syndrome 35 0.790
912
c LKM005 Leukemia, T-Cell, Chronic 33 0.790
913
c ACT042 Acute Pyelonephritis 45 0.789
914
P BNG032 Benign Mesothelioma 53 0.781
915
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.780
916
MCR191 Microscopic Colitis 46 0.780
917
IRT001 Iritis 45 0.780
918
P GRV001 Graves' Disease 54 0.773
919
P PNM006 Pneumoconiosis 55 0.769
920
ANT018 Anthracosis 51 0.769
921
HRT037 Heart and Brain Malformation Syndrome 32 0.769
922
c MJR024 Major Affective Disorder 9 40 0.769
923
c MJR022 Major Affective Disorder 8 37 0.769
924
IMM001 Immune-Complex Glomerulonephritis 36 0.769
925
P BPL003 Bipolar Disorder 56 0.769
926
P ORT004 Orthostatic Intolerance 62 0.769
927
P THY032 Thyroiditis 56 0.769
928
MTH047 Methanol Poisoning 37 0.769
929
PRM226 Primary Central Nervous System Lymphoma 47 0.768
930
PST092 Posttransplant Acute Limbic Encephalitis 29 0.762
931
PLM180 Pulmonary Artery Disease 34 0.761
932
INT303 Intracranial Hypertension, Idiopathic 56 0.758
933
ATN005 Autonomic Dysfunction 45 0.757
934
LWF001 Low-Flow Priapism 16 0.757
935
EXR008 Exercise-Induced Malignant Hyperthermia 20 0.757
936
DFF031 Diffuse Alveolar Hemorrhage 31 0.757
937
MCR088 Microscopic Polyangiitis 51 0.753
938
CHR020 Chronic Interstitial Cystitis 36 0.746
939
TBR011 Tuberculous Meningitis 48 0.746
940
HTS002 Heat-Shock Rna 1 9 0.745
941
MSC162 Muscular Dystrophy, Congenital Merosin-Deficient, 1a 55 0.745
942
c VSC019 Vesicoureteral Reflux 1 56 0.745
943
KRT008 Keratopathy 46 0.745
944
MCL003 Macular Holes 44 0.745
945
c CNG112 Congenital Muscular Dystrophy Type 1a 32 0.745
947
FCT007 Factor Vii Deficiency 64 0.742
948
DYS165 Dysfibrinogenemia, Congenital 51 0.742
949
P MLT020 Multiple Sclerosis 79 0.742
950
LFT001 Left Bundle Branch Hemiblock 47 0.740
951
CRY004 Cryoglobulinemia 47 0.740
952
LYM133 Lymphoma, Hodgkin, Classic 74 0.733
953
NRL016 Neural Tube Defects 81 0.733