Search results for thrombosis

1618 hits were found for thrombosis

# Family MCID Name MIFTS Score
1
THR024 Thrombosis 57 7.474
2
c THR092 Thrombophilia Due to Thrombin Defect 54 5.750
3
SGT001 Sagittal Sinus Thrombosis 35 5.718
4
INT078 Intracranial Thrombosis 36 5.687
5
PRT018 Portal Vein Thrombosis 49 5.460
6
CRN017 Coronary Thrombosis 48 5.376
7
LTR002 Lateral Sinus Thrombosis 26 4.955
8
CVR002 Cavernous Sinus Thrombosis 28 4.675
9
CRT004 Carotid Artery Thrombosis 40 4.511
10
INT076 Intracranial Sinus Thrombosis 24 3.835
11
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 18 3.281
12
THR055 Thrombophilia, X-Linked, Due to Factor Ix Defect 16 3.267
13
P BDD001 Budd-Chiari Syndrome 56 2.906
14
CRB132 Cerebral Sinovenous Thrombosis 31 2.190
15
FCT013 Factor V Leiden Thrombophilia 22 1.927
16
HMC020 Homocystinuria, B6-Responsive and Nonresponsive Types 43 1.902
17
VNS012 Venous Thoracic Outlet Syndrome 15 1.902
18
CRB009 Cerebritis 39 0.427
19
VND001 Vein Disease 47 0.260
20
PLM033 Pulmonary Embolism 60 0.259
21
P MYC007 Myocardial Infarction 79 0.227
22
P HPT021 Hepatitis 69 0.219
23
VSC007 Vascular Disease 67 0.219
24
P THR015 Thrombophilia 59 0.219
25
PRT014 Protein S Deficiency 53 0.216
26
P THR014 Thrombocytopenia 64 0.206
27
HPR003 Heparin-Induced Thrombocytopenia 45 0.197
28
PRT011 Protein C Deficiency 52 0.185
29
P ANT006 Antiphospholipid Syndrome 56 0.184
30
P HPT023 Hepatocellular Carcinoma 92 0.177
31
ANR040 Aneurysm 57 0.167
32
END072 Endotheliitis 42 0.151
33
P ESS003 Essential Thrombocythemia 70 0.149
34
c SYS001 Systemic Lupus Erythematosus 86 0.144
35
P LPS004 Lupus Erythematosus 64 0.143
36
HYP037 Hyperhomocysteinemia 50 0.143
37
PST095 Post-Thrombotic Syndrome 47 0.141
38
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.138
39
LVR012 Liver Cirrhosis 67 0.134
40
c ACT075 Acute Myocardial Infarction 60 0.129
41
P NPH012 Nephrotic Syndrome 59 0.129
42
P LKM002 Leukemia 71 0.125
43
VSC006 Vascular Cancer 51 0.122
44
CRD118 Cardiovascular Cancer 44 0.120
45
P PNC044 Pancreatitis 61 0.119
46
P PLY018 Polycythemia 58 0.118
47
ART111 Artery Disease 55 0.118
48
ISC004 Ischemia 61 0.117
49
CLT003 Colitis 60 0.114
50
PRP027 Peripheral Vascular Disease 68 0.113
51
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 62 0.113
52
P PRT013 Portal Hypertension 60 0.113
53
HMG002 Hemoglobinuria 48 0.113
54
ATH003 Atherosclerosis 65 0.111
55
THR016 Thrombophlebitis 53 0.111
56
ULC004 Ulcerative Colitis 76 0.108
57
HDC001 Headache 54 0.108
58
P CRN211 Coronary Artery Disease 74 0.104
59
BLD053 Blood Platelet Disease 46 0.104
60
HPT020 Hepatic Vascular Disease 42 0.104
61
P BLD051 Blood Coagulation Disease 42 0.104
62
VSC008 Vascular Hemostatic Disease 30 0.104
63
P SNS014 Sinusitis 60 0.102
64
P MNN013 Meningitis 67 0.096
65
RTN023 Retinitis 50 0.096
66
P HRT032 Heart Disease 75 0.095
67
MYL031 Myeloproliferative Neoplasm 58 0.095
68
THR004 Thrombocytosis 55 0.095
69
P LVR013 Liver Disease 75 0.093
70
MST019 Mastoiditis 32 0.093
71
P INF037 Inflammatory Bowel Disease 63 0.091
72
P HYP098 Hypereosinophilic Syndrome 63 0.091
73
DSS009 Disseminated Intravascular Coagulation 51 0.091
74
OTT002 Otitis Media 66 0.090
75
INT003 Intracranial Hypotension 34 0.090
76
P LYM118 Lymphoma 69 0.088
77
P ADN016 Adenocarcinoma 69 0.086
78
P VNS003 Venous Insufficiency 54 0.086
79
CLL003 Cellulitis 51 0.086
80
HDN002 Head Injury 45 0.086
81
P ART084 Arteriovenous Fistula 44 0.086
82
PRP030 Purpura 58 0.084
83
OVR029 Ovarian Hyperstimulation Syndrome 61 0.082
84
P HMC002 Homocystinuria 50 0.082
85
TBR010 Tuberculosis 70 0.081
86
INT075 Intracranial Hypertension 50 0.081
87
SPN340 Spontaneous Intracranial Hypotension 26 0.079
88
STR067 Stroke, Ischemic 75 0.077
89
ART021 Arteriosclerosis 58 0.077
90
P OBS005 Obesity 92 0.075
91
c CRN214 Coronary Heart Disease 5 22 0.075
92
P DYS026 Dysfibrinogenemia 45 0.072
93
ADJ001 Adjustment Disorder 38 0.072
94
CRN006 Coronary Aneurysm 32 0.072
95
c MYC058 Myocardial Infarction 2 28 0.072
96
c ADL096 Adult Hepatocellular Carcinoma 24 0.072
97
P PLM037 Pulmonary Hypertension 79 0.070
98
P LYM026 Lymphoblastic Leukemia 62 0.070
99
c ACT027 Acute Pancreatitis 57 0.068
100
MYM001 Myoma 52 0.068
101
THR013 Thoracic Outlet Syndrome 50 0.068
102
PPL021 Papilledema 47 0.068
103
CRD137 Cardiogenic Shock 46 0.068
104
P CRN178 Coronary Heart Disease 6 21 0.068
105
c CRN175 Coronary Heart Disease 4 19 0.068
106
P MYL005 Myelofibrosis 67 0.066
107
P ATR011 Atrial Fibrillation 66 0.066
108
CSY001 C Syndrome 50 0.066
109
ANG054 Angina Pectoris 50 0.066
110
SPL006 Splenic Infarction 35 0.066
111
SPR035 Superior Vena Cava Syndrome 31 0.066
112
ORB006 Orbital Cellulitis 26 0.066
113
DFC004 Deficiency Anemia 64 0.063
114
VSC011 Vasculitis 62 0.063
115
P HMP007 Hemophilia 57 0.063
116
IRN001 Iron Deficiency Anemia 52 0.063
117
P RNL014 Renal Cell Carcinoma 82 0.061
118
CRH001 Crohn's Disease 75 0.061
119
ISC006 Ischemic Heart Disease 68 0.061
120
P MYL006 Myeloid Leukemia 66 0.061
121
P GLM007 Glomerulonephritis 59 0.061
122
PTN001 Patent Foramen Ovale 55 0.061
123
CYT008 Cytomegalovirus Infection 52 0.061
124
FCT004 Factor Xii Deficiency 50 0.061
125
P OST028 Osteochondroma 47 0.061
126
CRB085 Cerebral Hemorrhage 46 0.061
127
CRT015 Carotid Artery Occlusion 43 0.061
128
ART005 Arteriovenous Malformation 66 0.058
129
CRB039 Cerebrovascular Disease 63 0.058
130
PRT036 Peritonitis 63 0.058
131
P INT030 Intracranial Aneurysm 54 0.058
132
KDS001 Kid Syndrome 53 0.058
133
P SPS003 Spastic Diplegia 52 0.058
134
ATR060 Atrial Standstill, Digenic 51 0.058
135
P CRN074 Coronary Artery Aneurysm 46 0.058
136
ALR002 Al-Raqad Syndrome 36 0.058
137
MYT019 May-Thurner Syndrome 23 0.058
138
KWS002 Kawasaki Disease 70 0.056
139
ART016 Aortic Aneurysm 69 0.056
140
P CRD011 Cardiomyopathy 68 0.056
141
P HYD006 Hydrocephalus 66 0.056
142
PLY125 Polycythemia Vera, Somatic 63 0.056
143
FCT007 Factor Vii Deficiency 61 0.056
144
P ENC018 Encephalopathy 59 0.056
145
CHL071 Child Syndrome 58 0.056
146
P HYP083 Hypopituitarism 54 0.056
147
P CRV039 Cervicitis 45 0.056
148
VSC047 Vascular Malformation 45 0.056
149
HRT012 Heart Valve Disease 40 0.056
150
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.056
151
c PRM225 Primary Thrombocytopenia 39 0.056
152
PRP080 Peripheral Artery Disease 37 0.056
153
SRC014 Sarcoma 66 0.053
154
P THL005 Thalassemia 64 0.053
155
c HMP029 Hemophilia a 63 0.053
156
P NRP001 Neuropathy 59 0.053
157
ART017 Aortic Disease 57 0.053
158
CHL067 Cholecystitis 57 0.053
159
SCK005 Sickle Cell Disease 51 0.053
160
HYP063 Hypersplenism 48 0.053
161
c CHR431 Chronic Venous Insufficiency 44 0.053
162
LMR001 Lemierre's Syndrome 43 0.053
163
CHR466 Chronic Thromboembolic Pulmonary Hypertension 39 0.053
164
CLP006 Clopidogrel Resistance 39 0.053
165
ABD004 Abdominal Tuberculosis 32 0.053
166
SPH007 Sphenoid Sinusitis 25 0.053
167
c CRN174 Coronary Heart Disease 2 20 0.053
168
P BRS047 Breast Cancer 100 0.050
169
P ART022 Arthritis 75 0.050
170
P APL001 Aplastic Anemia 75 0.050
171
MYL009 Myelodysplastic Syndrome 73 0.050
172
OST017 Osteomyelitis 61 0.050
173
VNW001 Von Willebrand's Disease 61 0.050
174
P HYP076 Hyperthyroidism 55 0.050
175
P HRD011 Hereditary Spherocytosis 54 0.050
176
P END033 Endocarditis 54 0.050
177
TTH006 Tooth Disease 52 0.050
178
P PYL005 Pyelonephritis 52 0.050
179
P AFB001 Afibrinogenemia 48 0.050
180
SPH001 Sapho Syndrome 46 0.050
181
P ABD003 Abdominal Aortic Aneurysm 45 0.050
182
SPP008 Suppurative Otitis Media 45 0.050
183
THR035 Thrombasthenia 39 0.050
184
PLM027 Pulmonary Embolism and Infarction 24 0.050
185
P LNG032 Lung Cancer 95 0.046
186
P MLT019 Multiple Myeloma 83 0.046
187
P PHC003 Pheochromocytoma 71 0.046
188
c HPT001 Hepatitis C 68 0.046
189
P PNM007 Pneumonia 68 0.046
190
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.046
191
c HPT016 Hepatitis B 64 0.046
192
SPN186 Spinal Cord Injury 63 0.046
193
P ASP006 Aspergillosis 61 0.046
194
HYP066 Hyperglycemia 61 0.046
195
BHC003 Behcet Syndrome 60 0.046
196
P HMR003 Hemorrhagic Disease 57 0.046
197
ORL011 Oral Cancer 56 0.046
198
HPT019 Hepatic Encephalopathy 56 0.046
199
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.046
200
ADL002 Adult Syndrome 52 0.046
201
BRN106 Burns 52 0.046
202
PRP016 Paraplegia 49 0.046
203
CHL069 Cholesteatoma 49 0.046
204
BCT015 Bacteremia 48 0.046
205
HRT007 Heart Cancer 46 0.046
206
PRP007 Priapism 46 0.046
207
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.046
208
EXS001 Exostosis 42 0.046
209
ERY004 Erysipelas 41 0.046
210
MDS022 Mediastinitis 41 0.046
211
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.046
212
CRB086 Cerebral Aneurysms 39 0.046
213
RTR011 Retroperitoneal Fibrosis 39 0.046
214
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.046
215
P RTN022 Retinal Vein Occlusion 38 0.046
216
HPT081 Hepatic Infarction 34 0.046
217
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 33 0.046
218
ZYG002 Zygomycosis 33 0.046
219
P HRT017 Heart Tumor 32 0.046
220
INT010 Intracranial Embolism 32 0.046
221
PTR001 Petrositis 24 0.046
222
c THR023 Thrombophilia Due to Thrombomodulin Defect 19 0.046
223
c ADL079 Adult Heart Tumor 16 0.046
224
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.043
225
P LPR003 Leprosy 69 0.043
226
P KDN018 Kidney Disease 66 0.043
227
c HMP004 Hemophilia B 62 0.043
228
P ESP024 Esophagitis 61 0.043
229
CRD119 Cardiac Arrest 61 0.043
230
TYP007 Typhoid Fever 61 0.043
231
APP008 Appendicitis 60 0.043
232
c ACT073 Acute Leukemia 60 0.043
233
MRB003 Morbid Obesity 58 0.043
234
SCH014 Schistosomiasis 58 0.043
235
P INT070 Intestinal Obstruction 57 0.043
236
PRS047 Prostatitis 56 0.043
237
P MMB011 Membranous Nephropathy 54 0.043
238
NWC001 Newcastle Disease 54 0.043
239
BLR001 Biliary Atresia 52 0.043
240
INT007 Intermediate Coronary Syndrome 50 0.043
241
THR104 Thrombophilia Due to Antithrombin Iii Deficiency 49 0.043
242
LMB062 Limb Ischemia 48 0.043
243
OCL006 Ocular Hypertension 48 0.043
244
THL018 Thalassemia Major 48 0.043
245
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.043
246
SPL012 Splenic Disease 46 0.043
247
ANR004 Anuria 45 0.043
248
CRB004 Cerebral Artery Occlusion 45 0.043
249
c ACT042 Acute Pyelonephritis 45 0.043
250
CRD001 Cardiac Tamponade 44 0.043
251
SPL018 Splenomegaly 44 0.043
252
PRT019 Protein-Losing Enteropathy 42 0.043
253
DDN006 Duodenitis 42 0.043
254
GST071 Gastrointestinal Carcinoma 42 0.043
255
CDQ001 Cauda Equina Syndrome 41 0.043
256
LCK001 Locked-in Syndrome 38 0.043
257
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 37 0.043
258
HMC014 Homocysteinemia 35 0.043
259
c FRN011 Frontal Sinusitis 31 0.043
260
WRF003 Warfarin Syndrome 28 0.043
261
EYC003 Eye Accommodation Disease 24 0.043
262
HRD083 Hereditary Antithrombin Deficiency 21 0.043
263
c CRN177 Coronary Heart Disease 7 20 0.043
264
c CRN173 Coronary Heart Disease 8 18 0.043
265
HGH021 Hughes-Stovin Syndrome 18 0.043
266
c CRN176 Coronary Heart Disease 9 18 0.043
267
THR088 Thrombophilia Due to Protein S Deficiency, Autosomal Recessive 18 0.043
268
THN005 Thunderclap Headache 16 0.043
269
CGL001 Coagulation Protein Disease 14 0.043
270
ORB016 Orbital Varix 12 0.043
271
CNG034 Congestive Heart Failure 72 0.039
272
SCK003 Sickle Cell Anemia 71 0.039
273
TTR001 Tetralogy of Fallot 71 0.039
274
c HYP595 Hypertension, Essential 69 0.039
275
PCK002 Pick Disease 68 0.039
276
P TRN020 Turner Syndrome 65 0.039
277
HMT002 Hematologic Cancer 64 0.039
278
GLN010 Glanzmann Thrombasthenia 63 0.039
279
P HML002 Hemolytic Anemia 62 0.039
280
P SLP006 Sleep Apnea 61 0.039
281
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 60 0.039
282
RBR001 Roberts Syndrome 60 0.039
283
P SHR029 Short Syndrome 58 0.039
284
ADN018 Adenoma 58 0.039
285
FCT006 Factor V Deficiency 57 0.039
286
HYP266 Hypoxia 56 0.039
287
INT079 Intrahepatic Cholangiocarcinoma 56 0.039
288
BLD034 Bile Duct Carcinoma 56 0.039
289
P LMY004 Leiomyosarcoma 55 0.039
290
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.039
291
P THY032 Thyroiditis 54 0.039
292
NRT004 Neuritis 52 0.039
293
BRN071 Brain Injury 52 0.039
294
PRC013 Pericarditis 51 0.039
295
VRC001 Varicocele 51 0.039
296
CRN030 Coronary Stenosis 51 0.039
297
NDL013 Nodular Regenerative Hyperplasia 50 0.039
298
RDC002 Radiculopathy 50 0.039
299
OPT009 Optic Neuritis 50 0.039
300
c ACT134 Acute Liver Failure 50 0.039
301
HLL004 Hellp Syndrome 50 0.039
302
KLN001 Klinefelter's Syndrome 50 0.039
303
MCR088 Microscopic Polyangiitis 49 0.039
304
PRN021 Paranasal Sinus Disease 49 0.039
305
CHR001 Churg-Strauss Syndrome 49 0.039
306
LPD004 Lipoid Nephrosis 48 0.039
307
URM002 Uremia 48 0.039
308
FSC004 Fasciitis 48 0.039
309
P CMP008 Compartment Syndrome 48 0.039
310
CHL004 Cholelithiasis 48 0.039
311
CCN002 Cocaine Abuse 48 0.039
312
ACR041 Acromelic Frontonasal Dysostosis 45 0.039
313
ALN001 Aland Island Eye Disease 45 0.039
314
P RTN014 Retinal Artery Occlusion 44 0.039
315
BRT030 Birth Defects 43 0.039
316
BCK006 Back Pain 43 0.039
317
GLC008 Glucose Metabolism Disease 42 0.039
318
SPR007 Superior Mesenteric Artery Syndrome 41 0.039
319
BRN080 Brain Ischemia 41 0.039
320
ACT055 Actinomycosis 40 0.039
321
ESN020 Eosinophilic Granulomatosis with Polyangiitis 39 0.039
322
BRS090 Breast Reconstruction 38 0.039
323
NSL022 Nasal Cavity Disease 38 0.039
324
SCR015 Scarlet Fever 38 0.039
325
BLD054 Blood Protein Disease 37 0.039
326
ISC002 Ischemic Optic Neuropathy 37 0.039
327
MDY003 Mody, Type Ii 36 0.039
328
c CNT016 Central Retinal Vein Occlusion 36 0.039
329
INF013 Inferior Myocardial Infarction 35 0.039
330
CRT012 Cortical Blindness 35 0.039
331
SPN185 Spinal Cord Infarction 34 0.039
332
P ACT080 Acute Pulmonary Heart Disease 31 0.039
333
SBD001 Subdural Empyema 30 0.039
334
CRB031 Cerebral Arterial Disease 27 0.039
335
c THR048 Thrombocytopenia 4 26 0.039
336
c CHR036 Chronic Cholangitis 26 0.039
337
THR068 Thrombophilia Due to Protein C Deficiency, Autosomal Recessive 26 0.039
338
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.039
339
VNF001 Vein of Galen Aneurysm 23 0.039
340
SNG003 Single Ventricular Heart 22 0.039
341
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 21 0.039
342
ABD009 Abducens Palsy 19 0.039
343
P ACT061 Acute Sphenoidal Sinusitis 14 0.039
344
P CLR023 Colorectal Cancer 97 0.035
345
P PNC035 Pancreatic Cancer 87 0.035
346
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.035
347
GST053 Gastric Cancer 78 0.035
348
c HPT073 Hepatitis C Virus 73 0.035
349
P CLC005 Celiac Disease 68 0.035
350
P MYP004 Myopathy 67 0.035
351
MLD001 Melioidosis 67 0.035
352
BRC012 Brucellosis 66 0.035
353
DWN001 Down Syndrome 66 0.035
354
P BCL006 B-Cell Lymphomas 65 0.035
355
P ART023 Arthropathy 64 0.035
356
P CNJ013 Conjunctivitis 64 0.035
357
P ENC004 Encephalitis 63 0.035
358
MLN008 Melanoma 62 0.035
359
GST092 Gastroesophageal Reflux 62 0.035
360
P LYM025 Lymphedema 61 0.035
361
P PSR002 Psoriasis 61 0.035
362
P MYM002 Moyamoya Disease 61 0.035
363
c ATM010 Autoimmune Hemolytic Anemia 60 0.035
364
P TMP003 Temporal Arteritis 60 0.035
365
ACQ007 Acquired Immunodeficiency Syndrome 60 0.035
366
c SYS004 Systemic Mastocytosis 60 0.035
367
SPT004 Septic Arthritis 60 0.035
368
P ORL007 Oral Cavity Cancer 59 0.035
369
P GRV001 Graves' Disease 59 0.035
370
CRN036 Craniopharyngioma 59 0.035
371
WLL006 Wells Syndrome 59 0.035
372
LPD008 Lipid Metabolism Disorder 58 0.035
373
P MTR012 Mitral Valve Disease 58 0.035
374
LYM021 Lymphadenitis 58 0.035
375
RHB003 Rhabdomyosarcoma 57 0.035
376
EXF001 Exfoliation Syndrome 57 0.035
377
WST001 West Syndrome 57 0.035
378
PRT093 Proteus Syndrome, Somatic 56 0.035
379
P MST009 Mastocytosis 56 0.035
380
PLS011 Plasmacytoma 56 0.035
381
PHR003 Pharyngitis 56 0.035
382
PRP019 Peripheral Nervous System Disease 55 0.035
383
MCS002 Mucositis 55 0.035
384
c THR082 Thrombophilia Due to Activated Protein C Resistance 54 0.035
385
KLP010 Klippel-Trenaunay-Weber Syndrome 54 0.035
386
CHL127 Cholangiocarcinoma, Susceptibility to 54 0.035
387
ESP023 Esophageal Disease 54 0.035
388
c ART101 Aortic Valve Disease 2 53 0.035
389
LYM040 Lymphoblastic Lymphoma 53 0.035
390
HYP080 Hypogonadism 53 0.035
391
P EXP004 Exophthalmos 53 0.035
392
LYM019 Lymphosarcoma 53 0.035
393
P PLY041 Polymyositis 52 0.035
394
BRN004 Brain Edema 52 0.035
395
TRM010 Traumatic Brain Injury 52 0.035
396
P PNC001 Pancytopenia 52 0.035
397
PMS001 Poems Syndrome 52 0.035
398
CRH005 Crohn's Colitis 52 0.035
399
CHC001 Chickenpox 51 0.035
400
MYL001 Myelitis 51 0.035
401
PYD001 Pyoderma Gangrenosum 51 0.035
402
HMP005 Hemiplegia 51 0.035
403
BNM001 Bone Marrow Cancer 51 0.035
404
BNF002 Bone Fracture 50 0.035
405
RLP001 Relapsing Polychondritis 50 0.035
406
MCN001 Mucinous Adenocarcinoma 50 0.035
407
PMP001 Pemphigus 50 0.035
408
END021 Endomyocardial Fibrosis 49 0.035
409
PYD002 Pyoderma 48 0.035
410
ACT017 Acute Chest Syndrome 48 0.035
411
P RNV001 Renovascular Hypertension 47 0.035
412
SDD007 Sudden Cardiac Death 47 0.035
413
SYN036 Syncope 47 0.035
414
SPN035 Spindle Cell Sarcoma 47 0.035
415
ART004 Aortic Atherosclerosis 46 0.035
416
ANG018 Angiomyolipoma 46 0.035
417
P CRN035 Cranial Nerve Palsy 46 0.035
418
CHR074 Choriocarcinoma 46 0.035
419
P PLN008 Peeling Skin Syndrome 45 0.035
420
ESN011 Eisenmenger Syndrome 45 0.035
421
SGN002 Signet Ring Cell Adenocarcinoma 45 0.035
422
EBS001 Ebstein Anomaly 45 0.035
423
VTM002 Vitamin B12 Deficiency 44 0.035
424
GDS001 Good Syndrome 44 0.035
425
FBR019 Fibromatosis 43 0.035
426
HYD012 Hydrops Fetalis 43 0.035
427
ART031 Aortic Coarctation 43 0.035
428
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.035
429
ACT058 Active Peptic Ulcer Disease 43 0.035
430
MYH001 May-Hegglin Anomaly 43 0.035
431
TRC023 Trichinosis 42 0.035
432
VGN023 Vaginitis 42 0.035
433
P CHL066 Cholangitis 42 0.035
434
P ERY048 Erythrocytosis, Familial, 2 42 0.035
435
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.035
436
PNM013 Pneumococcal Meningitis 41 0.035
437
CNV002 Conversion Disorder 41 0.035
438
NRN002 Neuronitis 41 0.035
439
P LBY004 Labyrinthitis 40 0.035
440
TRN012 Transient Global Amnesia 39 0.035
441
INT221 Intravascular Large B-Cell Lymphoma 38 0.035
442
SHW001 Shwartzman Phenomenon 37 0.035
443
BSL004 Basilar Artery Occlusion 36 0.035
444
CPL011 Capillary Malformations, Congenital, 1, Somatic, Mosaic 35 0.035
445
c THR037 Thrombocytopenia 2 35 0.035
446
IMP003 Impaired Renal Function Disease 34 0.035
447
ETH009 Ethmoid Sinusitis 34 0.035
448
EPD005 Epidural Abscess 33 0.035
449
MND006 Mondor Disease 21 0.035
450
THR089 Thrombophilia Due to Protein S Deficiency, Autosomal Dominant 20 0.035
451
DBL009 Double Inferior Vena Cava 19 0.035
452
THR067 Thrombophilia Due to Protein C Deficiency, Autosomal Dominant 19 0.035
453
c CRN172 Coronary Heart Disease 3 19 0.035
454
THR007 Thrombophlebitis Migrans 17 0.035
455
NNT044 Neonatal Antiphospholipid Syndrome 16 0.035
456
WSC001 Wisconsin Syndrome 14 0.035
457
HRD147 Hereditary Thrombophilia Due to Congenital Protein S Deficiency 11 0.035
458
P RHM011 Rheumatoid Arthritis 89 0.030
459
CYS001 Cystic Fibrosis 83 0.030
460
P MDL005 Medulloblastoma 77 0.030
461
P OVR042 Ovarian Cancer 76 0.030
462
c CHR090 Chronic Lymphocytic Leukemia 76 0.030
463
MNT001 Mantle Cell Lymphoma 72 0.030
464
P NRF002 Neurofibromatosis 71 0.030
465
BRK010 Burkitt Lymphoma 69 0.030
466
P FML011 Familial Adenomatous Polyposis 68 0.030
467
c NRF018 Neurofibromatosis, Type 1 67 0.030
468
P TBR001 Tuberous Sclerosis 67 0.030
469
P END044 Endometriosis 66 0.030
470
CRB037 Cerebral Palsy 66 0.030
471
OBS061 Obstructive Sleep Apnea 66 0.030
472
SKN016 Skin Disease 66 0.030
473
DRM006 Dermatitis 66 0.030
474
OBS002 Obsessive-Compulsive Disorder 66 0.030
475
ATP002 Atopy 66 0.030
476
P MSC005 Muscular Dystrophy 65 0.030
477
P AST007 Astrocytoma 65 0.030
478
P HYP086 Hypothyroidism 64 0.030
479
P PRD008 Periodontitis 63 0.030
480
P EHL001 Ehlers-Danlos Syndrome 63 0.030
481
LPT001 Leptospirosis 62 0.030
482
CNN005 Connective Tissue Disease 62 0.030
483
GNG013 Gingivitis 61 0.030
484
HYP056 Hypoglycemia 61 0.030
485
P HYP117 Hypertriglyceridemia 61 0.030
486
P ANR007 Anorexia Nervosa 61 0.030
487
P INT068 Intestinal Disease 60 0.030
488
TXC005 Toxic Shock Syndrome 60 0.030
489
P GST049 Gastrointestinal System Cancer 60 0.030
490
c VRL010 Viral Hepatitis 60 0.030
491
WLL001 Williams-Beuren Syndrome 60 0.030
492
P HMN010 Hemangioma 59 0.030
493
c FML001 Familial Atrial Fibrillation 58 0.030
494
RSP006 Respiratory System Disease 58 0.030
495
P CTR002 Cataract 58 0.030
496
MLG056 Malignant Hyperthermia 58 0.030
497
c PNC108 Pancreatitis, Hereditary 58 0.030
498
P THR003 Thoracic Aortic Aneurysm 57 0.030
499
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 57 0.030
500
CRT016 Carotid Artery Disease 57 0.030
501
P RBL001 Rubella 57 0.030
502
UTR039 Uterine Fibroid 57 0.030
503
P ANP001 Anaplastic Large Cell Lymphoma 57 0.030
504
TNS005 Tonsillitis 57 0.030
505
c PRC016 Pre-Eclampsia 56 0.030
506
TRN015 Transient Cerebral Ischemia 56 0.030
507
GST050 Gastrointestinal System Disease 56 0.030
508
P LPS002 Liposarcoma 55 0.030
509
P FNC043 Fanconi Anemia, Complementation Group E 55 0.030
510
ECH003 Echinococcosis 54 0.030
511
P MYC008 Myocarditis 54 0.030
512
c BCT007 Bacterial Meningitis 54 0.030
513
DBN001 Dubin-Johnson Syndrome 54 0.030
514
PLM010 Pulmonary Edema 54 0.030
515
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.030
516
P ECL001 Eclampsia 54 0.030
517
PLV003 Pelvic Inflammatory Disease 54 0.030
518
P PLY014 Polycystic Kidney Disease 53 0.030
519
P CRV031 Cervical Adenocarcinoma 53 0.030
520
BRG013 Buerger Disease 53 0.030
521
P DBT005 Diabetes Insipidus 53 0.030
522
P NNT009 Neonatal Diabetes Mellitus 52 0.030
523
c HPT015 Hepatitis D 52 0.030
524
GST040 Gastric Adenocarcinoma 52 0.030
525
P PRT096 Peritoneal Mesothelioma 52 0.030
526
P APL006 Aplasia Cutis Congenita 52 0.030
527
P TRT010 Teratoma 52 0.030
528
P OVR046 Ovarian Cyst 51 0.030
529
ASP003 Aseptic Meningitis 51 0.030
530
P PMP005 Pemphigus Vulgaris 51 0.030
531
VSC044 Visceral Myopathy 51 0.030
532
PRC012 Pericardial Effusion 51 0.030
533
END031 Endometrial Stromal Sarcoma 50 0.030
534
FCL012 Facial Paralysis 50 0.030
535
HND003 Hand-Foot-Uterus Syndrome 50 0.030
536
HPT046 Hepatic Veno-Occlusive Disease 50 0.030
537
RHM028 Rheumatic Heart Disease 50 0.030
538
MVM001 Movement Disease 49 0.030
539
P SHR001 Short Bowel Syndrome 49 0.030
540
GSG001 Gas Gangrene 49 0.030
541
CMR002 Coumarin Resistance 48 0.030
542
MTN003 Motion Sickness 48 0.030
543
P CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 48 0.030
544
OBS001 Obstructive Jaundice 48 0.030
545
PRT029 Parathyroid Adenoma 48 0.030
546
P ENC008 Encephalocele 48 0.030
547
P TRC086 Trichohepatoenteric Syndrome 1 48 0.030
548
HST009 Histiocytoma 47 0.030
549
P HMR005 Hemorrhoid 47 0.030
550
MNN009 Meningoencephalitis 47 0.030
551
HYD002 Hydronephrosis 47 0.030
552
c MLG069 Malignant Hypertension 47 0.030
553
P SYR001 Syringomyelia 47 0.030
554
CYS014 Cystadenocarcinoma 47 0.030
555
c MLG002 Malignant Peritoneal Mesothelioma 46 0.030
556
ALV002 Alveolar Echinococcosis 46 0.030
557
NCR007 Necrotizing Fasciitis 46 0.030
558
CVR006 Cavernous Hemangioma 46 0.030
559
CRY004 Cryoglobulinemia 46 0.030
560
STS002 Situs Inversus 46 0.030
561
ADN027 Adenomyosis 46 0.030
562
MGC001 Megacolon 45 0.030
563
URT010 Ureteral Obstruction 45 0.030
564
c CLR085 Colorectal Cancer 1 45 0.030
565
P END047 Endophthalmitis 45 0.030
566
SMN007 Seminoma 45 0.030
567
PRS045 Prostatic Hypertrophy 45 0.030
568
SND002 Sneddon Syndrome 44 0.030
569
PRN011 Pernicious Anemia 44 0.030
570
OCL069 Ocular Motor Apraxia 44 0.030
571
SPL004 Splenic Marginal Zone Lymphoma 44 0.030
572
c HMG003 Hemoglobin E Disease 44 0.030
573
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 43 0.030
574
PHY002 Physical Disorder 43 0.030
575
EVN001 Evans' Syndrome 43 0.030
576
DDN010 Duodenum Cancer 43 0.030
577
c ACQ014 Acquired Hemophilia 42 0.030
578
LMY003 Leiomyomatosis 42 0.030
579
NRR001 Neuroretinitis 42 0.030
580
HPT008 Hepatic Tuberculosis 42 0.030
581
SXL003 Sexual Disorder 42 0.030
582
HPT067 Hepatocellular Adenoma 42 0.030
583
TRN007 Transsexualism 41 0.030
584
MCR225 Macrophage Activation Syndrome 41 0.030
585
ESP002 Esophageal Varix 41 0.030
586
ALX001 Alexia 40 0.030
587
STR077 Streptococcal Toxic-Shock Syndrome 40 0.030
588
CYS009 Cystadenoma 40 0.030
589
c PLN018 Peeling Skin Syndrome 2 40 0.030
590
GND003 Gonadal Disease 39 0.030
591
P ATM020 Autoimmune Enteropathy 39 0.030
592
HMN016 Hemangioendothelioma 39 0.030
593
P MXL015 Maxillary Sinusitis 38 0.030
594
SCT001 Sciatic Neuropathy 38 0.030
595
BRN026 Branch Retinal Artery Occlusion 38 0.030
596
SPC003 Specific Developmental Disorder 38 0.030
597
SXD001 Sex Differentiation Disease 38 0.030
598
WTH001 Withdrawal Disorder 37 0.030
599
P PRX010 Paroxysmal Ventricular Fibrillation 37 0.030
600
PRL008 Paralytic Ileus 37 0.030
601
c CNT028 Central Retinal Artery Occlusion 37 0.030
602
PRC010 Pericardial Mesothelioma 37 0.030
603
ALC005 Alcoholic Pancreatitis 36 0.030
604
NNT024 Neonatal Stroke 36 0.030
605
c SBC003 Subacute Bacterial Endocarditis 36 0.030
606
BLR027 Blue Rubber Bleb Nevus 36 0.030
607
TTL010 Total Anomalous Pulmonary Venous Return 35 0.030
608
SBS006 Sebastian Syndrome 35 0.030
609
LYM005 Lymphocele 35 0.030
610
LYM014 Lymphangitis 35 0.030
611
OBS004 Obstructive Hydrocephalus 34 0.030
612
PLY131 Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes 34 0.030
613
CNS002 Constrictive Pericarditis 34 0.030
614
MSN003 Mesenteric Vascular Occlusion 34 0.030
615
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 34 0.030
616
c ACT036 Acute Cholangitis 34 0.030
617
LNG095 Lung Abscess 34 0.030
618
c DYS165 Dysfibrinogenemia, Congenital 34 0.030
619
PLX004 Plexopathy 34 0.030
620
BWN006 Bowen's Disease 33 0.030
621
HRS011 Horseshoe Kidney 33 0.030
622
MYS004 Myiasis 33 0.030
623
P CHR084 Chromosomal Disease 32 0.030
624
PRN039 Paraneoplastic Syndromes 32 0.030
625
HNS001 Hansen's Disease 30 0.030
626
STC016 Sticky Platelet Syndrome 29 0.030
627
c CNT068 Central Pain Syndrome 29 0.030
628
DNT046 Dental Abscess 28 0.030
629
MLK004 Malakoplakia 28 0.030
630
TXC001 Toxic Megacolon 28 0.030
631
WDS002 Woods Syndrome 27 0.030
632
PRM008 Parametritis 27 0.030
633
c THR102 Thrombocytopenia 5 27 0.030
634
FBR028 Fibrosing Mediastinitis 25 0.030
635
NDL010 Nodular Hidradenoma 25 0.030
636
NRS005 Neurosarcoidosis 23 0.030
637
WND002 Wandering Spleen 21 0.030
638
MTH044 Mthfr Gene Mutation 21 0.030
639
c RNL016 Renal Infectious Disease 20 0.030
640
c ACT035 Acute Frontal Sinusitis 20 0.030
641
THR020 Thrombophilia Due to Heparin Cofactor Ii Deficiency 19 0.030
642
AND005 Androgen Insensitivity Syndrome, Mild 16 0.030
643
PRN017 Perianal Hematoma 16 0.030
644
ACT174 Acute Peripheral Arterial Occlusion 15 0.030
645
c ANT041 Antiphospholipid Syndrome, Familial 14 0.030
646
CRT056 Carotidynia 14 0.030
647
OCL024 Ocular Neuromyotonia 13 0.030
648
P PRS040 Prostate Cancer 90 0.025
649
MLR004 Malaria 83 0.025
650
HV1006 Hiv-1 80 0.025
651
DCH001 Duchenne Muscular Dystrophy 79 0.025
652
HDG012 Hodgkin Lymphoma 77 0.025
653
c DLT002 Dilated Cardiomyopathy 76 0.025
654
c LKM061 Leukemia, Acute Myeloid 73 0.025
655
P WSK001 Wiskott-Aldrich Syndrome 73 0.025
656
P HMC003 Hemochromatosis 72 0.025
657
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.025
658
P INF038 Influenza 72 0.025
659
PTZ001 Peutz-Jeghers Syndrome 71 0.025
660
ADN021 Adenomatous Polyposis Coli 70 0.025
661
P NRB001 Neuroblastoma 70 0.025
662
CRZ001 Crouzon Syndrome 70 0.025
663
BCK001 Becker Muscular Dystrophy 69 0.025
664
TST021 Testicular Germ Cell Tumor 69 0.025
665
P DMN001 Diamond-Blackfan Anemia 69 0.025
666
FBR012 Fabry Disease 69 0.025
667
SVR004 Severe Combined Immunodeficiency 69 0.025
668
P OST005 Osteogenesis Imperfecta 69 0.025
669
P GLB002 Glioblastoma 68 0.025
670
PLM001 Pulmonary Tuberculosis 67 0.025
671
c CHR089 Chronic Kidney Failure 66 0.025
672
P LYM007 Lymphangioleiomyomatosis 66 0.025
673
P CSH001 Cushing's Syndrome 65 0.025
674
P KDN017 Kidney Cancer 65 0.025
675
P HRP006 Herpes Simplex 65 0.025
676
CNT098 Central Core Disease 65 0.025
677
P AMY004 Amyloidosis 65 0.025
678
P PLY011 Polycystic Ovary Syndrome 65 0.025
679
P SPN046 Spinal Muscular Atrophy 65 0.025
680
LNG099 Lung Disease 64 0.025
681
P CRB042 Cerebellar Ataxia 63 0.025
682
P DYS007 Dyskeratosis Congenita 63 0.025
683
P ALX003 Alexander Disease 63 0.025
684
WGN006 Wegener Granulomatosis 63 0.025
685
GLB015 Glioblastoma Multiforme 63 0.025
686
P PRT010 Parathyroid Carcinoma 63 0.025
687
c ATS347 Autosomal Dominant Polycystic Kidney Disease 62 0.025
688
P LNG064 Lung Cancer Susceptibility 3 62 0.025
689
MXD005 Mixed Connective Tissue Disease 62 0.025
690
P ATP001 Atopic Dermatitis 62 0.025
691
P DRM010 Dermatomyositis 62 0.025
692
P PRD006 Prader-Willi Syndrome 62 0.025
693
LSC001 Lesch-Nyhan Syndrome 61 0.025
694
MTH009 Mouth Disease 61 0.025
695
ORN006 Ornithine Transcarbamylase Deficiency 61 0.025
696
P FCL005 Focal Segmental Glomerulosclerosis 60 0.025
697
DRR010 Darier Disease 60 0.025
698
P GLM045 Glioma 60 0.025
699
P PLC011 Pilocytic Astrocytoma 60 0.025
700
P VNT002 Ventricular Septal Defect 60 0.025
701
c HPT003 Hepatitis a 59 0.025
702
P HRM001 Hermansky-Pudlak Syndrome 59 0.025
703
P NTR004 Neutropenia 59 0.025
704
STT001 Status Epilepticus 59 0.025
705
LGN002 Legionellosis 59 0.025
706
ADL030 Adult-Onset Still's Disease 59 0.025
707
P PRP029 Porphyria 59 0.025
708
P RTN025 Retinoschisis 58 0.025
709
P HYP060 Hyperinsulinism 58 0.025
710
P MCR010 Microcephaly 58 0.025
711
P UVT001 Uveitis 58 0.025
712
ING001 Inguinal Hernia 58 0.025
713
CTS003 Coats Disease 57 0.025
714
ADM013 Adamantinoma of Long Bones 57 0.025
715
SFT003 Soft Tissue Sarcoma 57 0.025
716
CRT002 Cartilage-Hair Hypoplasia 57 0.025
717
c ACT210 Acute Respiratory Distress Syndrome 57 0.025
718
P MYS005 Myositis 57 0.025
719
ARG002 Argininosuccinic Aciduria 57 0.025
720
P SZR006 Seizure Disorder 56 0.025
721
HRP004 Herpes Zoster 56 0.025
722
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 56 0.025
723
P ACT074 Acute Lymphocytic Leukemia 56 0.025
724
INT002 Intermittent Claudication 56 0.025
725
P OLG002 Oligodendroglioma 56 0.025
726
P GST044 Gastritis 56 0.025
727
NRN004 Neuroendocrine Tumor 56 0.025
728
P PLY006 Polydactyly 56 0.025
729
P CHN012 Chondrosarcoma 56 0.025
730
GST023 Gastric Ulcer 56 0.025
731
c MLG077 Malignant Peripheral Nerve Sheath Tumor 56 0.025
732
P OVR049 Ovarian Disease 56 0.025
733
JNT002 Joint Disorders 55 0.025
734
CCC001 Coccidioidomycosis 55 0.025
735
P SCL018 Scoliosis 55 0.025
736
JPN002 Japanese Encephalitis 55 0.025
737
HPT022 Hepatoblastoma 55 0.025
738
END030 End Stage Renal Failure 55 0.025
739
SCR008 Scrub Typhus 55 0.025
740
P MNC007 Monocytic Leukemia 55 0.025
741
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 54 0.025
742
RCT018 Rectal Neoplasm 54 0.025
743
c PND001 Pain Disorder 54 0.025
744
APH002 Aphasia 54 0.025
745
GST037 Gastroparesis 54 0.025
746
P HYP620 Hypoprothrombinemia 54 0.025
747
PTT046 Pituitary Hormone Deficiency, Combined, 2 54 0.025
748
MCN017 Meconium Ileus 54 0.025
749
CMP010 Complex Regional Pain Syndrome 54 0.025
750
LMY002 Leiomyoma 54 0.025
751
NTH001 Netherton Syndrome 54 0.025
752
CYS005 Cysticercosis 54 0.025
753
TST014 Testicular Cancer 53 0.025
754
PTT049 Pituitary Adenoma, Acth-Secreting 53 0.025
755
P SYP003 Syphilis 53 0.025
756
P ATX004 Ataxia 53 0.025
757
CHL014 Cholera 53 0.025
758
TLN003 Telangiectasis 52 0.025
759
P SML016 Small Intestine Cancer 52 0.025
760
GTR002 Goiter 52 0.025
761
BLM002 Bulimia Nervosa 52 0.025
762
ERD001 Erdheim-Chester Disease 52 0.025
763
UTR024 Uterine Carcinosarcoma 52 0.025
764
QDR001 Quadriplegia 52 0.025
765
IMP002 Imperforate Anus 52 0.025
766
P ANG015 Angioedema 52 0.025
767
ALL026 Allergic Hypersensitivity Disease 52 0.025
768
MCN007 Meconium Aspiration Syndrome 52 0.025
769
c ACT009 Acute Monocytic Leukemia 52 0.025
770
c PRM012 Primary Polycythemia 52 0.025
771
P PRM006 Primary Biliary Cirrhosis 51 0.025
772
P ERY008 Erythromelalgia 51 0.025
773
CRT049 Critical Limb Ischemia 51 0.025
774
P PTS002 Ptosis 51 0.025
775
ANK001 Ankylosis 51 0.025
776
P STR020 Strabismus 51 0.025
777
P GND004 Gonadal Dysgenesis 51 0.025
778
PNN001 Panniculitis 51 0.025
779
SRS001 Serous Cystadenocarcinoma 51 0.025
780
CLR109 Colorectal Adenocarcinoma 51 0.025
781
P PRM002 Primary Hyperoxaluria 51 0.025
782
MYL020 Myelomeningocele 51 0.025
783
INF034 Infective Endocarditis 51 0.025
784
STM006 Stomach Disease 50 0.025
785
c ART115 Aortic Valve Disease 1 50 0.025
786
GRW007 Growth Hormone Deficiency 50 0.025
787
KMR001 Kimura Disease 50 0.025
788
CLN015 Colon Adenocarcinoma 50 0.025
789
AMN001 Amenorrhea 50 0.025
790
P RST002 Restrictive Cardiomyopathy 50 0.025
791
CCT002 Cicatricial Pemphigoid 50 0.025
792
P MSC003 Muscular Atrophy 50 0.025
793
MCR004 Macroglobulinemia 50 0.025
794
RNL007 Renal Tubular Acidosis 50 0.025
795
URN009 Urinary System Disease 50 0.025
796
P CLL015 Collagen Disease 50 0.025
797
LPR001 Lepromatous Leprosy 50 0.025
798
DFF036 Differentiated Thyroid Carcinoma 50 0.025
799
P PNV001 Panuveitis 50 0.025
800
DRG003 Drug Dependence 50 0.025
801
HPT074 Hepatic Adenoma, Somatic 50 0.025
802
PLC005 Placental Insufficiency 50 0.025
803
RNL024 Renal Glucosuria 50 0.025
804
P URF003 Urofacial Syndrome 1 50 0.025
805
P TRN034 Transverse Myelitis 49 0.025
806
VNW005 Von Willebrand Disease, Type 1 49 0.025
807
EXT010 Extramedullary Plasmacytoma 49 0.025
808
c ACT071 Acute Kidney Failure 49 0.025
809
WHP001 Whipple Disease 49 0.025
810
c CNG411 Congenital Disorder of Glycosylation, Type in 49 0.025
811
ALC009 Alcoholic Liver Cirrhosis 49 0.025
812
P INT063 Intellectual Disability 49 0.025
813
ILT001 Ileitis 49 0.025
814
CHL061 Childhood Leukemia 49 0.025
815
TRN044 Transposition of the Great Arteries 48 0.025
816
MCP006 Mucoepidermoid Carcinoma 48 0.025
817
P FML035 Familial Hyperlipidemia 48 0.025
818
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 48 0.025
819
QBC001 Quebec Platelet Disorder 48 0.025
820
PLS009 Plasma Cell Neoplasm 48 0.025
821
PSD007 Pseudomyxoma Peritonei 48 0.025
822
BRK001 Brooke-Spiegler Syndrome 48 0.025
823
JCB001 Jacobsen Syndrome 48 0.025
824
RFL001 Reflex Sympathetic Dystrophy 48 0.025
825
FML039 Female Reproductive System Disease 48 0.025
826
P RNL015 Renal Hypertension 48 0.025
827
c HMG001 Hemoglobin C Disease 47 0.025
828
CRN027 Corneal Neovascularization 47 0.025
829
P VGN017 Vaginal Cancer 47 0.025
830
c INV001 Invasive Aspergillosis 47 0.025
831
INT253 Intestinal Benign Neoplasm 47 0.025
832
GST009 Gastroschisis 47 0.025
833
PLC007 Placental Abruption 47 0.025
834
TBR011 Tuberculous Meningitis 47 0.025
835
MGR028 Migraine with or Without Aura 1 47 0.025
836
UPP004 Upper Respiratory Tract Disease 46 0.025
837
c OST135 Osteogenesis Imperfecta, Type I 46 0.025
838
ERY045 Erythrocytosis, Somatic 46 0.025
839
CLC001 Calciphylaxis 46 0.025
840
INT067 Interstitial Nephritis 46 0.025
841
SML036 Small Intestinal Adenocarcinoma 46 0.025
842
c PST005 Posterior Uveitis 46 0.025
843
BBS001 Babesiosis 46 0.025
844
P ACT150 Acute Adrenal Insufficiency 45 0.025
845
EPT020 Epithelioid Hemangioendothelioma 45 0.025
846
CLL002 Collecting Duct Carcinoma 45 0.025
847
P MLG086 Malignant Hyperthermia Susceptibility 45 0.025
848
BRN014 Bronchopneumonia 45 0.025
849
DVR002 Diverticulitis 45 0.025
850
RFR010 Refractory Anemia 45 0.025
851
HNC001 Henoch-Schoenlein Purpura 45 0.025
852
P ATR005 Atrophic Gastritis 45 0.025
853
MXD023 Mixed Cell Type Cancer 44 0.025
854
ENC044 Enchondromatosis, Multiple, Ollier Type 44 0.025
855
END020 Endocardial Fibroelastosis 44 0.025
856
P SDR002 Siderosis 44 0.025
857
CNG048 Congenital Hepatic Fibrosis 44 0.025
858
RTN001 Retinal Vasculitis 44 0.025
859
PLC001 Placenta Accreta 44 0.025
860
DRM013 Dermoid Cyst 44 0.025
861
P PSD003 Pseudohypoaldosteronism 44 0.025
862
c GRV008 Graves Disease 1 44 0.025
863
LYM012 Lymphoplasmacytic Lymphoma 44 0.025
864
CLS010 Cluster Headache 44 0.025
865
PRM020 Premenstrual Tension 44 0.025
866
LFT009 Left Ventricular Outflow Tract Obstruction 43 0.025
867
CRR007 Cirrhosis, Cryptogenic 43 0.025
868
TBR006 Tuberculoid Leprosy 43 0.025
869
MTS001 Mutism 43 0.025
870
ERY029 Erythermalgia, Primary 43 0.025
871
PLR005 Pleuropneumonia 43 0.025
872
HDR006 Hidradenocarcinoma 43 0.025
873
MTR003 Mitral Valve Stenosis 43 0.025
874
FCT005 Factor Xiii Deficiency 43 0.025
875
P MGS004 Meige Syndrome 43 0.025
876
FBR003 Fibrous Histiocytoma 43 0.025
877
NPH010 Nephrosclerosis 43 0.025
878
P CRB088 Cerebral Atrophy 42 0.025
879
PRT026 Parotitis 42 0.025
880
BHR001 Behr Syndrome 42 0.025
881
EPS023 Epstein-Barr Virus-Associated Gastric Carcinoma 42 0.025
882
KLT001 Klatskin's Tumor 42 0.025
883
INT071 Intestinal Perforation 42 0.025
884
INT060 Intestinal Atresia 42 0.025
885
P HRN001 Horner's Syndrome 42 0.025
886
c HRD012 Hereditary Elliptocytosis 42 0.025
887
STR079 Sturge-Weber Syndrome, Somatic, Mosaic 42 0.025
888
FCT008 Factitious Disorder 41 0.025
889
PRM025 Primary Bacterial Infectious Disease 41 0.025
890
CRT008 Carotid Artery Dissection 41 0.025
891
RPR002 Reproductive System Disease 41 0.025
892
HMT018 Hematopoietic Stem Cell Transplantation 41 0.025
893
TBR008 Tuberculous Peritonitis 41 0.025
894
WBR001 Weber Syndrome 41 0.025
895
IDP070 Idiopathic Scoliosis 41 0.025
896
P PRP034 Purpura Fulminans 41 0.025
897
HST016 Histiocytic Sarcoma 40 0.025
898
PNC119 Pancreatic Neuroendocrine Tumor 40 0.025
899
BRN015 Bronchiolo-Alveolar Adenocarcinoma 40 0.025
900
MLN013 Melanoma Metastasis 40 0.025
901
THL017 Thalassemia Intermedia 40 0.025
902
P CYS017 Cystic Teratoma 40 0.025
903
CHR034 Chromophobe Adenoma 40 0.025
904
MLT145 Multiple Enchondromatosis, Maffucci Type 40 0.025
905
CNN002 Cannabis Abuse 40 0.025
906
MNN017 Mononeuropathy 40 0.025
907
PRG008 Paragonimiasis 40 0.025
908
PYM001 Pyomyositis 40 0.025
909
BRN118 Brain Small Vessel Disease with or Without Ocular Anomalies 40 0.025
910
c ACQ012 Acquired Angioedema 39 0.025
911
ADN002 Adenoiditis 39 0.025
912
GNT031 Genitopatellar Syndrome 39 0.025
913
BRS064 Bursitis 39 0.025
914
HYP319 Hypereosinophilic Syndrome, Idiopathic, Resistant to Imatinib 39 0.025
915
MSN002 Mesenteric Lymphadenitis 39 0.025
916
APP010 Appendix Cancer 39 0.025
917
ILC002 Ileocolitis 39 0.025
918
BLD032 Bile Duct Adenocarcinoma 39 0.025
919
ISC015 Ischemic Colitis 39 0.025
920
NRC019 Neurocutaneous Melanosis, Somatic 39 0.025
921
P HYP265 Hypotonia 38 0.025
922
P CHR342 Chiari Malformation 38 0.025
923
SCR001 Secretory Meningioma 38 0.025
924
c GST048 Gastrointestinal System Benign Neoplasm 38 0.025
925
c PSR017 Psoriasis 2 37 0.025
926
MYS001 Myositis Ossificans 37 0.025
927
P BRN035 Brain Stem Glioma 37 0.025
928
INT042 Internuclear Ophthalmoplegia 37 0.025
929
c HYP163 Hyperlipidemia Type 3 36 0.025
930
CNG069 Congenital Cytomegalovirus 36 0.025
931
VRT001 Vertebral Artery Occlusion 36 0.025
932
P CMM008 Communicating Hydrocephalus 36 0.025
933
ULN001 Ulnar Neuropathy 36 0.025
934
OVR054 Ovarian Mucinous Neoplasm 36 0.025
935
CRT013 Carotid Stenosis 36 0.025
936
PNC002 Pancreatic Mucinous Cystadenoma 36 0.025
937
NTR005 Nutritional Deficiency Disease 36 0.025
938
HYP015 Hyperlucent Lung 36 0.025
939
P MNN007 Meningocele 36 0.025
940
WLL004 Wallerian Degeneration 36 0.025
941
AGR018 Agraphia 36 0.025
942
AMP003 Ampulla of Vater Neoplasm 35 0.025
943
MTL002 Metal Metabolism Disorder 35 0.025
944
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.025
945
CHP002 Chops Syndrome 35 0.025
946
AMP007 Amphetamine Abuse 35 0.025
947
ACL001 Acalculous Cholecystitis 35 0.025
948
END075 Endocervical Adenocarcinoma 35 0.025
949
UTR020 Uterine Inversion 35 0.025
950
ANG017 Angiolipoma 35 0.025
951
GNT005 Giant Hemangioma 35 0.025
952
FRN014 Fournier Gangrene 35 0.025
953
PLY024 Polymicrogyria 35 0.025
954
INP001 Inappropriate Adh Syndrome 35 0.025
955
AMP009 Ampulla of Vater Adenocarcinoma 35 0.025
956
CPP003 Cap Polyposis 35 0.025
957
c PLN017 Peeling Skin Syndrome 1 34 0.025
958
PLM052 Pulmonary Arteriovenous Malformation 34 0.025
959
EMB002 Embryoma 34 0.025
960
c BRN108 Branchiootic Syndrome 1 34 0.025
961
c DFN114 Deafness, Autosomal Recessive 67 34 0.025
962
CRD016 Cardiac Rupture 34 0.025
963
SPR066 Superficial Siderosis 34 0.025
964
BLR005 Biliary Papillomatosis 34 0.025
965
FTD001 Foot Drop 33 0.025
966
BLD019 Bile Duct Cystadenocarcinoma 33 0.025
967
LYM011 Lymphogranuloma Venereum 33 0.025
968
CHR010 Chorioangioma 33 0.025
969
c MLT009 Multiple Cranial Nerve Palsy 33 0.025
970
DDN007 Duodenal Disease 33 0.025
971
ANT013 Anterior Spinal Artery Syndrome 33 0.025
972
MTL005 Metal Allergy 33 0.025
973
FNC006 Functional Gastric Disease 32 0.025
974
PSR005 Psoriasis, Protection Against 32 0.025
975
CHL070 Cholesterol Embolism 32 0.025
976
c HYP272 Hypercholesterolemia, Familial, 3 32 0.025
977
LVD002 Livedoid Vasculopathy 32 0.025
978
QLT001 Qualitative Platelet Defect 32 0.025
979
CLL009 Colloid Carcinoma of the Pancreas 32 0.025
980
c PSR019 Psoriasis Susceptibility 13 32 0.025
981
SRN001 Serine Deficiency 32 0.025
982
FLM001 Filamentary Keratitis 32 0.025
983
PRN007 Perinephritis 32 0.025
984
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 31 0.025
985
GPS001 Gapo Syndrome 31 0.025
986
c PST001 Posterior Myocardial Infarction 31 0.025
987
CHR076 Choriocarcinoma of the Testis 31 0.025
988
BLD005 Bile Duct Mucoepidermoid Carcinoma 31 0.025
989
GST017 Gastric Tubular Adenocarcinoma 31 0.025
990
INT020 Intravenous Leiomyomatosis 31 0.025
991
P PNC043 Pancreatic Intraductal Papillary-Mucinous Neoplasm 31 0.025
992
RNL001 Renal Artery Obstruction 31 0.025
993
c INF078 Inflammatory Bowel Disease 2 31 0.025
994
ART012 Aortitis 30 0.025
995
TST043 Testicular Seminoma 30 0.025
996
SPL007 Splenic Abscess 30 0.025
997
c ACQ010 Acquired Polycythemia 30 0.025
998
MYX006 Myxoid Leiomyosarcoma 30 0.025
999
BRW004 Brown-Sequard Syndrome 29 0.025
1000
INF133 Inferior Vena Cava Interruption 29 0.025
1001
MRG013 Mirage Syndrome 29 0.025
1002
BRW006 Brown Syndrome 29 0.025
1003
c PLN021 Peeling Skin Syndrome 3 29 0.025
1004
c TRC078 Trichohepatoenteric Syndrome 2 29 0.025
1005
HMN004 Hemangioma of Liver 29 0.025
1006
PRM243 Primary Bone Cancer 29 0.025
1007
GLY032 Glycosylphosphatidylinositol Deficiency 29 0.025
1008
ANL012 Anal Gland Adenocarcinoma 28 0.025
1009
SBC014 Subclavian Steal Syndrome 28 0.025
1010
XNT001 Xanthogranulomatous Pyelonephritis 28 0.025
1011
ANL014 Anal Canal Adenocarcinoma 28 0.025
1012
TMR001 Tumor of Exocrine Pancreas 28 0.025
1013
BRN055 Bronchogenic Cyst 28 0.025
1014
c CHR047 Chronic Ethmoiditis 28 0.025
1015
MDN008 Median Arcuate Ligament Syndrome 28 0.025
1016
RHS001 Rh Isoimmunization 28 0.025
1017
THY024 Thymus Adenocarcinoma 28 0.025
1018
P DCR004 Dacryocystitis 27 0.025
1019
CYS003 Cystitis Cystica 27 0.025
1020
BLD052 Blood Group Incompatibility 27 0.025
1021
SCL007 Sclerosing Hepatic Carcinoma 27 0.025
1022
SCR024 Sacrococcygeal Teratoma 27 0.025
1023
PMP008 Pemphigus Vegetans 27 0.025
1024
BRS010 Breast Mucoepidermoid Carcinoma 26 0.025
1025
PRT086 Partial Hydatidiform Mole 26 0.025
1026
DSC004 Discitis 26 0.025
1027
SVN001 Sveinsson Choreoretinal Atrophy 26 0.025
1028
LKM059 Leukemia, Megakaryoblastic, with or Without Down Syndrome, Somatic 26 0.025
1029
OVR011 Ovarian Mucinous Adenocarcinoma 26 0.025
1030
SPR032 Superficial Siderosis of the Central Nervous System 26 0.025
1031
ANS010 Anus Adenocarcinoma 26 0.025
1032
c ANR038 Anorexia Nervosa 1 26 0.025
1033
YNG002 Young Syndrome 26 0.025
1034
PRF003 Piriformis Syndrome 26 0.025
1035
49X002 49,xxxxy Syndrome 25 0.025
1036
MCN004 Mucinous Tubular and Spindle Renal Cell Carcinoma 25 0.025
1037
ALP072 Alpha-Fetoprotein Deficiency 25 0.025
1038
HMX002 Heme Oxygenase-1 Deficiency 25 0.025
1039
GST016 Gastric Signet Ring Cell Adenocarcinoma 24 0.025
1040
CNG134 Congenitally Corrected Transposition of the Great Arteries 24 0.025
1041
c PRT045 Prothrombin-Related Thrombophilia 24 0.025
1042
SBC002 Subclavian Artery Aneurysm 24 0.025
1043
SBS002 Substernal Goiter 24 0.025
1044
MNN005 Meningovascular Neurosyphilis 24 0.025
1045
PLM058 Pulmonary Atresia with Intact Ventricular Septum 24 0.025
1046
RVR002 Reversible Cerebral Vasoconstriction Syndrome 24 0.025
1047
HMC012 Hemicrania Continua 23 0.025
1048
CNT067 Central Cord Syndrome 23 0.025
1049
ABD002 Abducens Nerve Disease 23 0.025
1050
CRT028 Cor Triatriatum 22 0.025
1051
MCN005 Mucinous Intrahepatic Cholangiocarcinoma 22 0.025
1052
CVR001 Cavernous Sinus Meningioma 22 0.025
1053
CHR158 Charles Bonnet Syndrome 22 0.025
1054
ATR024 Atrial Fibrillation and Stroke 22 0.025
1055
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 21 0.025
1056
CRB087 Cerebral Arteriosclerosis 21 0.025
1057
MCN003 Mucinous Ovarian Cystadenoma 21 0.025
1058
CNG298 Congenital Pancreatic Cyst 21 0.025
1059
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 21 0.025
1060
PNT023 Pontine Hemorrhage 21 0.025
1061
CGH002 Cough Headache 20 0.025
1062
HPT066 Hepatoportal Sclerosis 20 0.025
1063
STN013 Stenotrophomonas Maltophilia Infection 20 0.025
1064
CCN009 Cocaine Intoxication 20 0.025
1065
ANG066 Angel-Shaped Phalangoepiphyseal Dysplasia 20 0.025
1066
PRX023 Paroxysmal Nocturnal Hemoglobinuria, Somatic 20 0.025
1067
ACR079 Acrodysostosis with Multiple Hormone Resistance 19 0.025
1068
VSC009 Vascular Skin Disease 19 0.025
1069
ART109 Arterial Thoracic Outlet Syndrome 18 0.025
1070
PGM028 Pigmented Purpuric Dermatosis 18 0.025
1071
MTH028 Mthfr Thermolabile Variant 18 0.025
1072
MXD035 Mixed-Type Autoimmune Hemolytic Anemia 17 0.025
1073
THR021 Thrombophilia Due to Hrg Deficiency 17 0.025
1074
INT055 Intravascular Fasciitis 17 0.025
1075
PLS001 Pulsating Exophthalmos 16 0.025
1076
FMR002 Femoral Cancer 16 0.025
1077
BNT001 Banti's Syndrome 16 0.025
1078
CNG092 Congenital Extrahepatic Portosystemic Shunt 15 0.025
1079
c BLR016 Biliary Cirrhosis, Primary, 2 15 0.025
1080
FXL001 Foix-Alajouanine Syndrome 15 0.025
1081
CRD023 Cardiomyopathy Cataract Hip Spine Disease 15 0.025
1082
48X002 48,xxxy Syndrome 14 0.025
1083
MCN006 Mucinous Adenofibroma 14 0.025
1084
PRP050 Peripheral Arterial Occlusive Disease 1 14 0.025
1085
ANG062 Angioosteohypertrophic Syndrome 14 0.025
1086
CNG171 Congenital Plasminogen Deficiency 14 0.025
1087
c BLR026 Biliary Cirrhosis, Primary, 5 14 0.025
1088
DRL001 Dural Sinus Malformation 14 0.025
1089
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 13 0.025
1090
TMP006 Temporomandibular Ankylosis 13 0.025
1091
HMC030 Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency 13 0.025
1092
NVS004 Nova Syndrome 13 0.025
1093
BRS103 Bier Spots 12 0.025
1094
PLM062 Pulmonary Hyalinizing Granuloma 12 0.025
1095
FNC050 Functioning Gonadotropic Adenoma 12 0.025
1096
c SLC030 Slc6a4-Related Altered Drug Metabolism 11 0.025
1097
CYS035 Cystic Adventitial Disease 11 0.025
1098
MNT045 Montefiore Syndrome 10 0.025
1099
P OST012 Osteoarthritis 83 0.018
1100
P HNT016 Huntington Disease 80 0.018
1101
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 78 0.018
1102
P RTT002 Rett Syndrome 77 0.018
1103
ESP021 Esophageal Cancer 76 0.018
1104
P HYP607 Hypercholesterolemia, Familial 76 0.018
1105
GST019 Gastrointestinal Stromal Tumor 73 0.018
1106
WLS001 Wilson Disease 72 0.018
1107
P NRV007 Nervous System Disease 71 0.018
1108
c FNC027 Fanconi Anemia, Complementation Group a 71 0.018
1109
P PRK057 Parkinson Disease, Late-Onset 70 0.018
1110
CRV047 Cervical Cancer, Somatic 65 0.018
1111
P PLR004 Pleuropulmonary Blastoma 65 0.018
1112
P PRM019 Premature Ovarian Failure 64 0.018
1113
P HLP001 Holoprosencephaly 63 0.018
1114
OST085 Osteosarcoma, Somatic 63 0.018
1115
GLL018 Gallbladder Cancer 63 0.018
1116
P ADD001 Addison's Disease 62 0.018
1117
P NRV006 Nervous System Cancer 60 0.018
1118
PRM097 Primary Immunodeficiency Disease 60 0.018
1119
LPM004 Lipoma 60 0.018
1120
OCL009 Ocular Cancer 59 0.018
1121
CNT097 Central Hypoventilation Syndrome, Congenital 59 0.018
1122
GST045 Gastroenteritis 59 0.018
1123
P OCL013 Oculodentodigital Dysplasia 59 0.018
1124
P INF032 Infertility 59 0.018
1125
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.018
1126
c ESS001 Essential Tremor 59 0.018
1127
P HYP069 Hyperparathyroidism 58 0.018
1128
DMN031 Dementia, Lewy Body 58 0.018
1129
PNC034 Pancreas Disease 58 0.018
1130
BNC003 Bone Cancer 58 0.018
1131