Search results for thrombosis

1273 hits were found for thrombosis

# Family MCID Name MIFTS Score
1
THR024 Thrombosis 61 7.821
2
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 7.372
3
c THR092 Thrombophilia Due to Thrombin Defect 61 6.382
4
INT078 Intracranial Thrombosis 37 5.837
5
SGT001 Sagittal Sinus Thrombosis 34 5.626
6
PRT018 Portal Vein Thrombosis 50 5.476
7
CRN017 Coronary Thrombosis 48 5.298
8
CVR002 Cavernous Sinus Thrombosis 28 5.018
9
LTR002 Lateral Sinus Thrombosis 24 4.869
10
CRT004 Carotid Artery Thrombosis 37 4.438
11
INT076 Intracranial Sinus Thrombosis 25 3.754
12
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 25 3.231
13
BDD001 Budd-Chiari Syndrome 58 2.871
14
PRM285 Primitive Portal Vein Thrombosis 14 2.676
15
THR055 Thrombophilia, X-Linked, Due to Factor Ix Defect 15 2.595
16
FCT024 Factor V Excess with Spontaneous Thrombosis 10 2.595
17
CRB132 Cerebral Sinovenous Thrombosis 32 2.193
18
HPT046 Hepatic Veno-Occlusive Disease 56 1.906
19
VNS012 Venous Thoracic Outlet Syndrome 18 1.859
20
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 44 1.848
21
CRB009 Cerebritis 41 0.504
22
VSC007 Vascular Disease 71 0.315
23
PLM033 Pulmonary Embolism 62 0.296
24
P MYC007 Myocardial Infarction 81 0.264
25
P THR015 Thrombophilia 58 0.260
26
P HPT021 Hepatitis 75 0.258
27
PRT014 Protein S Deficiency 47 0.253
28
P THR014 Thrombocytopenia 65 0.244
29
HPR003 Heparin-Induced Thrombocytopenia 48 0.236
30
P ANT006 Antiphospholipid Syndrome 59 0.220
31
PRT011 Protein C Deficiency 48 0.214
32
P HPT023 Hepatocellular Carcinoma 94 0.211
33
ANR040 Aneurysm 61 0.200
34
ANT009 Antithrombin Iii Deficiency 58 0.177
35
PST095 Post-Thrombotic Syndrome 52 0.177
36
END072 Endotheliitis 46 0.177
37
P ESS003 Essential Thrombocythemia 71 0.173
38
c SYS001 Systemic Lupus Erythematosus 86 0.166
39
P LPS004 Lupus Erythematosus 69 0.166
40
c BLD140 Blood Group, I System 37 0.161
41
LVR012 Liver Cirrhosis 73 0.160
42
P NPH012 Nephrotic Syndrome 60 0.155
43
P LKM002 Leukemia 75 0.147
44
ISC004 Ischemia 66 0.145
45
c ACT075 Acute Myocardial Infarction 64 0.145
46
P PNC044 Pancreatitis 64 0.141
47
PLY001 Polycythemia Vera 75 0.140
48
ART140 Arteries, Anomalies of 51 0.140
49
P PLY018 Polycythemia 60 0.138
50
THR016 Thrombophlebitis 53 0.138
51
P LVR013 Liver Disease 76 0.134
52
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.132
53
CLT003 Colitis 63 0.132
54
HDC001 Headache 55 0.132
55
HMG002 Hemoglobinuria 52 0.132
56
P PRT013 Portal Hypertension 59 0.129
57
ULC004 Ulcerative Colitis 80 0.126
58
P CRN018 Coronary Artery Anomaly 69 0.126
59
P SNS014 Sinusitis 62 0.123
60
DSS009 Disseminated Intravascular Coagulation 56 0.121
61
THR004 Thrombocytosis 55 0.118
62
AGN016 Aging 65 0.116
63
P MNN013 Meningitis 71 0.114
64
MYL031 Myeloproliferative Neoplasm 64 0.114
65
RTN023 Retinitis 52 0.114
66
LNG099 Lung Disease 67 0.112
67
STR067 Stroke, Ischemic 84 0.110
68
RSP006 Respiratory System Disease 63 0.110
69
P ART084 Arteriovenous Fistula 46 0.110
70
P ADN016 Adenocarcinoma 71 0.109
71
P HYP098 Hypereosinophilic Syndrome 65 0.109
72
INT075 Intracranial Hypertension 53 0.109
73
P HMC002 Homocystinuria 50 0.109
74
MST019 Mastoiditis 33 0.109
75
P LYM118 Lymphoma 71 0.107
76
P VNS003 Venous Insufficiency 53 0.107
77
INT003 Intracranial Hypotension 36 0.107
78
PRP027 Peripheral Vascular Disease 71 0.105
79
OTT002 Otitis Media 67 0.105
80
PRP030 Purpura 61 0.105
81
CLL003 Cellulitis 53 0.105
82
P INF037 Inflammatory Bowel Disease 52 0.105
83
P HRT032 Heart Disease 80 0.103
84
HDN002 Head Injury 48 0.101
85
P DYS026 Dysfibrinogenemia 51 0.099
86
LMR001 Lemierre's Syndrome 47 0.099
87
ISC006 Ischemic Heart Disease 73 0.097
88
OVR029 Ovarian Hyperstimulation Syndrome 64 0.097
89
VRC005 Varicose Veins 64 0.095
90
P ART021 Arteriosclerosis 62 0.095
91
P CRN300 Coronary Heart Disease 1 57 0.095
92
PPL021 Papilledema 50 0.095
93
SPN340 Spontaneous Intracranial Hypotension 28 0.092
94
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.090
95
P ATR011 Atrial Fibrillation 68 0.090
96
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.090
97
P HMP007 Hemophilia 61 0.090
98
ANG054 Angina Pectoris 53 0.090
99
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.090
100
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.090
101
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.090
102
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.090
103
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.090
104
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.090
105
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.090
106
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.090
107
FCT004 Factor Xii Deficiency 50 0.088
108
MYT019 May-Thurner Syndrome 27 0.088
109
P PLM037 Pulmonary Hypertension 79 0.086
110
P DBT009 Diabetes Mellitus 72 0.086
111
c ACT027 Acute Pancreatitis 61 0.086
112
THR013 Thoracic Outlet Syndrome 50 0.086
113
CRN006 Coronary Aneurysm 32 0.086
114
P MYL005 Myelofibrosis 75 0.083
115
P LYM026 Lymphoblastic Leukemia 66 0.083
116
FCT007 Factor Vii Deficiency 62 0.083
117
PTN001 Patent Foramen Ovale 58 0.083
118
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.083
119
P BLD051 Blood Coagulation Disease 38 0.083
120
ORB006 Orbital Cellulitis 29 0.083
121
c HMP029 Hemophilia a 69 0.081
122
VNW001 Von Willebrand's Disease 61 0.081
123
MYM001 Myoma 56 0.081
124
CRD137 Cardiogenic Shock 45 0.081
125
SPL006 Splenic Infarction 34 0.081
126
CRH001 Crohn's Disease 80 0.078
127
P MYC084 Mycobacterium Tuberculosis 1 69 0.078
128
BRG013 Buerger Disease 62 0.078
129
DFC004 Deficiency Anemia 62 0.078
130
IRN001 Iron Deficiency Anemia 55 0.078
131
P MMB011 Membranous Nephropathy 55 0.078
132
INT303 Intracranial Hypertension, Idiopathic 49 0.078
133
c THR082 Thrombophilia Due to Activated Protein C Resistance 47 0.078
134
THR035 Thrombasthenia 46 0.078
135
CRT015 Carotid Artery Occlusion 42 0.078
136
VSC011 Vasculitis 66 0.075
137
ART005 Arteriovenous Malformation 64 0.075
138
CYT008 Cytomegalovirus Infection 57 0.075
139
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.075
140
P CRV039 Cervicitis 49 0.075
141
CTS005 Catastrophic Antiphospholipid Syndrome 45 0.075
142
BLD053 Blood Platelet Disease 45 0.075
143
P MYL006 Myeloid Leukemia 69 0.073
144
CRB039 Cerebrovascular Disease 68 0.073
145
ACT119 Acute Promyelocytic Leukemia 64 0.073
146
P GLM007 Glomerulonephritis 61 0.073
147
P ENC018 Encephalopathy 58 0.073
148
HYP810 Hypereosinophilic Syndrome, Idiopathic 57 0.073
149
P OST028 Osteochondroma 51 0.073
150
P AFB001 Afibrinogenemia 49 0.073
151
IRN002 Iron Metabolism Disease 45 0.073
152
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.073
153
HPT081 Hepatic Infarction 30 0.073
154
c BTT014 Beta-Thalassemia 70 0.070
155
P ANR048 Aniridia 1 68 0.070
156
c HMP004 Hemophilia B 67 0.070
157
PRT036 Peritonitis 67 0.070
158
FCT002 Factor Xi Deficiency 64 0.070
159
P THR005 Thrombotic Thrombocytopenic Purpura 63 0.070
160
c AFB002 Afibrinogenemia, Congenital 61 0.070
161
P HMR003 Hemorrhagic Disease 61 0.070
162
P INT030 Intracranial Aneurysm 58 0.070
163
SPS003 Spastic Diplegia 55 0.070
164
SCK005 Sickle Cell Disease 54 0.070
165
P RTN022 Retinal Vein Occlusion 53 0.070
166
HMC014 Homocysteinemia 49 0.070
167
VND001 Vein Disease 48 0.070
168
P CRN074 Coronary Artery Aneurysm 47 0.070
169
c CHR431 Chronic Venous Insufficiency 47 0.070
170
INT010 Intracranial Embolism 38 0.070
171
HPR006 Heparin Cofactor Ii Deficiency 28 0.070
172
ANR038 Anorexia Nervosa 1 21 0.070
173
BLD137 Blood Group--Ahonen 17 0.070
174
c HPT001 Hepatitis C 73 0.067
175
KWS002 Kawasaki Disease 72 0.067
176
ART016 Aortic Aneurysm 70 0.067
177
P KDN018 Kidney Disease 69 0.067
178
RNL114 Renal Cell Carcinoma, Nonpapillary 68 0.067
179
P HYD006 Hydrocephalus 68 0.067
180
SRC014 Sarcoma 68 0.067
181
GLN010 Glanzmann Thrombasthenia 66 0.067
182
P HYP083 Hypopituitarism 59 0.067
183
P PYL005 Pyelonephritis 56 0.067
184
HLL004 Hellp Syndrome 53 0.067
185
HYP063 Hypersplenism 49 0.067
186
ISC002 Ischemic Optic Neuropathy 48 0.067
187
CHR466 Chronic Thromboembolic Pulmonary Hypertension 43 0.067
188
SPH007 Sphenoid Sinusitis 24 0.067
189
THR088 Thrombophilia Due to Protein S Deficiency, Autosomal Recessive 18 0.067
190
P ART022 Arthritis 77 0.064
191
GST050 Gastrointestinal System Disease 66 0.064
192
P THL005 Thalassemia 65 0.064
193
P NRP001 Neuropathy 63 0.064
194
P END033 Endocarditis 58 0.064
195
SPH001 Sapho Syndrome 54 0.064
196
NTR018 Neutrophilia, Hereditary 46 0.064
197
P RTN014 Retinal Artery Occlusion 45 0.064
198
SPN185 Spinal Cord Infarction 33 0.064
199
ABD004 Abdominal Tuberculosis 31 0.064
200
P BRS047 Breast Cancer 100 0.060
201
c LKM061 Leukemia, Acute Myeloid 81 0.060
202
MYL009 Myelodysplastic Syndrome 75 0.060
203
APL001 Aplastic Anemia 74 0.060
204
P PNM007 Pneumonia 70 0.060
205
c HPT016 Hepatitis B 68 0.060
206
OST017 Osteomyelitis 64 0.060
207
PMS001 Poems Syndrome 64 0.060
208
INT002 Intermittent Claudication 61 0.060
209
CHL067 Cholecystitis 58 0.060
210
P HYP076 Hyperthyroidism 56 0.060
211
P HRD011 Hereditary Spherocytosis 55 0.060
212
PRP016 Paraplegia 53 0.060
213
FCT006 Factor V Deficiency 52 0.060
214
c ACQ014 Acquired Hemophilia 51 0.060
215
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 51 0.060
216
SPP008 Suppurative Otitis Media 50 0.060
217
c CNT016 Central Retinal Vein Occlusion 50 0.060
218
PLM175 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 48 0.060
219
ESP002 Esophageal Varix 46 0.060
220
FCT005 Factor Xiii Deficiency 46 0.060
221
P PRP034 Purpura Fulminans 44 0.060
222
CLP006 Clopidogrel Resistance 42 0.060
223
PRT019 Protein-Losing Enteropathy 40 0.060
224
FRN014 Fournier Gangrene 38 0.060
225
MRN001 Marantic Endocarditis 37 0.060
226
BRN026 Branch Retinal Artery Occlusion 35 0.060
227
ASC009 Ascites, Chylous 35 0.060
228
GNT005 Giant Hemangioma 33 0.060
229
QLT001 Qualitative Platelet Defect 32 0.060
230
c INH004 Inherited Blood Coagulation Disease 29 0.060
231
P LNG032 Lung Cancer 99 0.057
232
MYL069 Myeloma, Multiple 86 0.057
233
P PHC003 Pheochromocytoma 72 0.057
234
BHC003 Behcet Syndrome 68 0.057
235
P PRT008 Proteus Syndrome 67 0.057
236
SPN186 Spinal Cord Injury 67 0.057
237
P ASP006 Aspergillosis 65 0.057
238
HYP066 Hyperglycemia 64 0.057
239
P ESP024 Esophagitis 64 0.057
240
c HPT003 Hepatitis a 63 0.057
241
CRD119 Cardiac Arrest 63 0.057
242
SCH014 Schistosomiasis 62 0.057
243
c ACT073 Acute Leukemia 61 0.057
244
HPT019 Hepatic Encephalopathy 59 0.057
245
FCT003 Factor X Deficiency 58 0.057
246
BRN106 Burns 57 0.057
247
P THY032 Thyroiditis 56 0.057
248
PRP080 Peripheral Artery Disease 54 0.057
249
P CHL069 Cholesteatoma 52 0.057
250
c ACT134 Acute Liver Failure 52 0.057
251
FCT001 Factor Viii Deficiency 50 0.057
252
PRP007 Priapism 49 0.057
253
SND002 Sneddon Syndrome 48 0.057
254
c ACT042 Acute Pyelonephritis 48 0.057
255
LCK001 Locked-in Syndrome 47 0.057
256
EXS001 Exostosis 46 0.057
257
DDN006 Duodenitis 46 0.057
258
MDS022 Mediastinitis 44 0.057
259
ERY004 Erysipelas 43 0.057
260
LCH001 Leech Infestation 43 0.057
261
ISC015 Ischemic Colitis 39 0.057
262
P BLD124 Bleeding Disorder, Platelet-Type, 11 38 0.057
263
BLT003 Blue Toe Syndrome 38 0.057
264
HPT020 Hepatic Vascular Disease 36 0.057
265
ZYG002 Zygomycosis 35 0.057
266
ALR002 Al-Raqad Syndrome 30 0.057
267
STC016 Sticky Platelet Syndrome 28 0.057
268
PTR001 Petrositis 25 0.057
269
THR089 Thrombophilia Due to Protein S Deficiency, Autosomal Dominant 23 0.057
270
P PNC035 Pancreatic Cancer 89 0.053
271
TYP007 Typhoid Fever 67 0.053
272
APP008 Appendicitis 64 0.053
273
MRB003 Morbid Obesity 61 0.053
274
PRS047 Prostatitis 59 0.053
275
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 58 0.053
276
IMM136 Immune System Disease 57 0.053
277
BLR001 Biliary Atresia 56 0.053
278
PRC013 Pericarditis 55 0.053
279
INT007 Intermediate Coronary Syndrome 55 0.053
280
c GRV008 Graves Disease 1 52 0.053
281
PYD002 Pyoderma 51 0.053
282
PLC007 Placental Abruption 50 0.053
283
ESN011 Eisenmenger Syndrome 49 0.053
284
ANR004 Anuria 49 0.053
285
c ERY048 Erythrocytosis, Familial, 2 48 0.053
286
c HYP805 Hypercholesterolemia, Autosomal Dominant, 3 47 0.053
287
PRT012 Prothrombin Deficiency 46 0.053
288
SPL018 Splenomegaly 45 0.053
289
RTR011 Retroperitoneal Fibrosis 43 0.053
290
CRB086 Cerebral Aneurysms 42 0.053
291
BRS090 Breast Reconstruction 41 0.053
292
CDQ001 Cauda Equina Syndrome 41 0.053
293
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.053
294
c DYS165 Dysfibrinogenemia, Congenital 37 0.053
295
LVD002 Livedoid Vasculopathy 36 0.053
296
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.053
297
c FRN011 Frontal Sinusitis 30 0.053
298
INT050 Intestinal Impaction 27 0.053
299
THR068 Thrombophilia Due to Protein C Deficiency, Autosomal Recessive 26 0.053
300
HRD083 Hereditary Antithrombin Deficiency 24 0.053
301
HGH021 Hughes-Stovin Syndrome 23 0.053
302
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.053
303
THN005 Thunderclap Headache 17 0.053
304
c THR023 Thrombophilia Due to Thrombomodulin Defect 16 0.053
305
ORB016 Orbital Varix 14 0.053
306
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.049
307
CNG034 Congestive Heart Failure 74 0.049
308
BRC012 Brucellosis 71 0.049
309
BRK010 Burkitt Lymphoma 71 0.049
310
CRB037 Cerebral Palsy 70 0.049
311
P BCL006 B-Cell Lymphomas 70 0.049
312
P TTR001 Tetralogy of Fallot 70 0.049
313
P TRN020 Turner Syndrome 69 0.049
314
P ART023 Arthropathy 68 0.049
315
P CNJ013 Conjunctivitis 67 0.049
316
ACQ007 Acquired Immunodeficiency Syndrome 65 0.049
317
P SLP006 Sleep Apnea 65 0.049
318
P PSR002 Psoriasis 65 0.049
319
c PRC016 Pre-Eclampsia 65 0.049
320
ADN018 Adenoma 63 0.049
321
P HML002 Hemolytic Anemia 62 0.049
322
HYP266 Hypoxia 61 0.049
323
KLP010 Klippel-Trenaunay-Weber Syndrome 60 0.049
324
PLS011 Plasmacytoma 60 0.049
325
LGG001 Legg-Calve-Perthes Disease 59 0.049
326
P LMY004 Leiomyosarcoma 59 0.049
327
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.049
328
MCR088 Microscopic Polyangiitis 58 0.049
329
INF034 Infective Endocarditis 56 0.049
330
RDC002 Radiculopathy 55 0.049
331
P INT070 Intestinal Obstruction 55 0.049
332
NRT004 Neuritis 55 0.049
333
OPT009 Optic Neuritis 53 0.049
334
CRD223 Cardiac Arrhythmia 52 0.049
335
URM002 Uremia 52 0.049
336
P CHL066 Cholangitis 52 0.049
337
LMB062 Limb Ischemia 52 0.049
338
VRC001 Varicocele 52 0.049
339
CHR001 Churg-Strauss Syndrome 51 0.049
340
CHL004 Cholelithiasis 51 0.049
341
CCN002 Cocaine Abuse 50 0.049
342
CHR074 Choriocarcinoma 49 0.049
343
FSC004 Fasciitis 48 0.049
344
PLC008 Placenta Disease 48 0.049
345
P CMP008 Compartment Syndrome 48 0.049
346
ESN020 Eosinophilic Granulomatosis with Polyangiitis 47 0.049
347
SDD008 Sudden Sensorineural Hearing Loss 46 0.049
348
CRD001 Cardiac Tamponade 45 0.049
349
MYH001 May-Hegglin Anomaly 45 0.049
350
ACT055 Actinomycosis 43 0.049
351
PYM001 Pyomyositis 42 0.049
352
INT221 Intravascular Large B-Cell Lymphoma 42 0.049
353
P CRN035 Cranial Nerve Palsy 42 0.049
354
KRN001 Korean Hemorrhagic Fever 42 0.049
355
PNM013 Pneumococcal Meningitis 40 0.049
356
SCR015 Scarlet Fever 40 0.049
357
PRP028 Peripheral Vertigo 37 0.049
358
GLY032 Glycosylphosphatidylinositol Deficiency 36 0.049
359
BSL004 Basilar Artery Occlusion 35 0.049
360
c HMG003 Hemoglobin E Disease 34 0.049
361
CRT012 Cortical Blindness 34 0.049
362
ANT013 Anterior Spinal Artery Syndrome 33 0.049
363
SBD001 Subdural Empyema 31 0.049
364
ABD009 Abducens Palsy 29 0.049
365
VNF001 Vein of Galen Aneurysm 27 0.049
366
THR067 Thrombophilia Due to Protein C Deficiency, Autosomal Dominant 23 0.049
367
P ACT061 Acute Sphenoidal Sinusitis 15 0.049
368
P CLR023 Colorectal Cancer 98 0.045
369
P MLT020 Multiple Sclerosis 85 0.045
370
P OVR042 Ovarian Cancer 82 0.045
371
c HPT073 Hepatitis C Virus 73 0.045
372
SCK003 Sickle Cell Anemia 73 0.045
373
MLD001 Melioidosis 73 0.045
374
MLN008 Melanoma 72 0.045
375
P MYP004 Myopathy 69 0.045
376
P TMP003 Temporal Arteritis 67 0.045
377
ATM095 Autoimmune Disease 66 0.045
378
P ENC004 Encephalitis 66 0.045
379
GST092 Gastroesophageal Reflux 64 0.045
380
CRN036 Craniopharyngioma 63 0.045
381
P LYM025 Lymphedema 63 0.045
382
P HYP086 Hypothyroidism 62 0.045
383
P GRV001 Graves' Disease 62 0.045
384
LYM021 Lymphadenitis 62 0.045
385
MCS002 Mucositis 61 0.045
386
P RHB003 Rhabdomyosarcoma 61 0.045
387
c PNC108 Pancreatitis, Hereditary 60 0.045
388
SPT004 Septic Arthritis 60 0.045
389
P BRN019 Bernard-Soulier Syndrome 60 0.045
390
P MTR012 Mitral Valve Disease 59 0.045
391
PHR003 Pharyngitis 59 0.045
392
PLC005 Placental Insufficiency 59 0.045
393
ALL026 Allergic Hypersensitivity Disease 59 0.045
394
VGN023 Vaginitis 59 0.045
395
LYM040 Lymphoblastic Lymphoma 58 0.045
396
LYM019 Lymphosarcoma 58 0.045
397
URN009 Urinary System Disease 58 0.045
398
ART017 Aortic Disease 57 0.045
399
P ECL001 Eclampsia 57 0.045
400
P PLY041 Polymyositis 57 0.045
401
HYP730 Hypogonadotropic Hypogonadism 56 0.045
402
BNF002 Bone Fracture 56 0.045
403
RLP001 Relapsing Polychondritis 55 0.045
404
P ERY058 Erythrocytosis, Familial, 1 55 0.045
405
PYD001 Pyoderma Gangrenosum 55 0.045
406
BRN071 Brain Injury 54 0.045
407
TRM010 Traumatic Brain Injury 54 0.045
408
HMP005 Hemiplegia 54 0.045
409
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 54 0.045
410
HYP080 Hypogonadism 54 0.045
411
c SVR005 Severe Pre-Eclampsia 53 0.045
412
NDL013 Nodular Regenerative Hyperplasia 53 0.045
413
EBS001 Ebstein Anomaly 52 0.045
414
P SHR001 Short Bowel Syndrome 52 0.045
415
MYL001 Myelitis 52 0.045
416
END021 Endomyocardial Fibrosis 51 0.045
417
OCL006 Ocular Hypertension 51 0.045
418
PRT129 Prothrombin Deficiency, Congenital 51 0.045
419
PLS009 Plasma Cell Neoplasm 51 0.045
420
P PRN026 Porencephaly 50 0.045
421
ACT017 Acute Chest Syndrome 50 0.045
422
EXP004 Exophthalmos 50 0.045
423
DBT084 Diabetes Mellitus, Ketosis-Prone 50 0.045
424
HYD012 Hydrops Fetalis 50 0.045
425
PNC001 Pancytopenia 50 0.045
426
ANG018 Angiomyolipoma 50 0.045
427
P RNV001 Renovascular Hypertension 48 0.045
428
CHC001 Chickenpox 48 0.045
429
ART031 Aortic Coarctation 48 0.045
430
CRB085 Cerebral Hemorrhage 47 0.045
431
VNW005 Von Willebrand Disease, Type 1 47 0.045
432
SYN036 Syncope 46 0.045
433
SPN035 Spindle Cell Sarcoma 46 0.045
434
VTM002 Vitamin B12 Deficiency 46 0.045
435
BCK006 Back Pain 46 0.045
436
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 46 0.045
437
RTN021 Retinal Vascular Occlusion 45 0.045
438
TRC023 Trichinosis 45 0.045
439
CMR002 Coumarin Resistance 44 0.045
440
MCR225 Macrophage Activation Syndrome 44 0.045
441
NRN002 Neuronitis 43 0.045
442
MNN021 Meningococcemia 43 0.045
443
P LBY004 Labyrinthitis 41 0.045
444
TRN012 Transient Global Amnesia 40 0.045
445
SHW001 Shwartzman Phenomenon 40 0.045
446
NNT024 Neonatal Stroke 38 0.045
447
c PRM225 Primary Thrombocytopenia 37 0.045
448
CNS002 Constrictive Pericarditis 37 0.045
449
INF013 Inferior Myocardial Infarction 36 0.045
450
CHR010 Chorioangioma 35 0.045
451
CRY036 Cryptogenic Cirrhosis 34 0.045
452
HYD059 Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect 34 0.045
453
PLT015 Platelet Aggregation, Spontaneous 32 0.045
454
EPD005 Epidural Abscess 31 0.045
455
PRG092 Pregnancy Loss, Recurrent 1 30 0.045
456
INF133 Inferior Vena Cava Interruption 28 0.045
457
P STR035 Streptococcal Group a Invasive Disease 28 0.045
458
MNN005 Meningovascular Neurosyphilis 26 0.045
459
BLD054 Blood Protein Disease 25 0.045
460
WND002 Wandering Spleen 24 0.045
461
BLD163 Blood Group, Dombrock System 23 0.045
462
CRV071 Cervical Rib 21 0.045
463
c ANT041 Antiphospholipid Syndrome, Familial 18 0.045
464
DBL009 Double Inferior Vena Cava 17 0.045
465
NNT044 Neonatal Antiphospholipid Syndrome 12 0.045
466
P RHM011 Rheumatoid Arthritis 91 0.040
467
CYS001 Cystic Fibrosis 85 0.040
468
GST053 Gastric Cancer 84 0.040
469
P INF038 Influenza 77 0.040
470
P MDL005 Medulloblastoma 76 0.040
471
MNT001 Mantle Cell Lymphoma 76 0.040
472
NRF026 Neurofibromatosis, Type Iv, of Riccardi 72 0.040
473
P FML011 Familial Adenomatous Polyposis 71 0.040
474
P END044 Endometriosis 71 0.040
475
WGN006 Wegener Granulomatosis 71 0.040
476
DWN001 Down Syndrome 70 0.040
477
CHL065 Cholangiocarcinoma 70 0.040
478
P TBR001 Tuberous Sclerosis 69 0.040
479
P AMY004 Amyloidosis 69 0.040
480
OBS002 Obsessive-Compulsive Disorder 68 0.040
481
c PLM164 Pulmonary Hypertension, Primary, 1 67 0.040
482
P PRD008 Periodontitis 67 0.040
483
DRM006 Dermatitis 67 0.040
484
P MSC005 Muscular Dystrophy 66 0.040
485
P AST007 Astrocytoma 66 0.040
486
P DRM010 Dermatomyositis 65 0.040
487
P INT068 Intestinal Disease 65 0.040
488
CNN005 Connective Tissue Disease 65 0.040
489
SYS004 Systemic Mastocytosis 65 0.040
490
LPT001 Leptospirosis 64 0.040
491
GNG013 Gingivitis 64 0.040
492
ADR054 Adrenocortical Carcinoma, Hereditary 63 0.040
493
c ACT210 Acute Respiratory Distress Syndrome 63 0.040
494
OST003 Osteonecrosis 63 0.040
495
HYP056 Hypoglycemia 62 0.040
496
P LPS002 Liposarcoma 61 0.040
497
P EHL001 Ehlers-Danlos Syndrome 61 0.040
498
TXC005 Toxic Shock Syndrome 61 0.040
499
P HMN010 Hemangioma 61 0.040
500
TNS005 Tonsillitis 61 0.040
501
P RBL001 Rubella 61 0.040
502
P GLM045 Glioma 61 0.040
503
P CTR002 Cataract 60 0.040
504
P MLG056 Malignant Hyperthermia 60 0.040
505
P PLY014 Polycystic Kidney Disease 60 0.040
506
BLD034 Bile Duct Carcinoma 60 0.040
507
ORL011 Oral Cancer 60 0.040
508
P ANP001 Anaplastic Large Cell Lymphoma 60 0.040
509
INT079 Intrahepatic Cholangiocarcinoma 60 0.040
510
P HMR012 Hemorrhagic Fever 60 0.040
511
c VRL010 Viral Hepatitis 59 0.040
512
P MNC007 Monocytic Leukemia 59 0.040
513
c BCT007 Bacterial Meningitis 59 0.040
514
P LPR021 Leprosy 3 59 0.040
515
P MYC008 Myocarditis 58 0.040
516
PTT046 Pituitary Hormone Deficiency, Combined, 2 57 0.040
517
THR100 Thrombocytopenic Purpura, Autoimmune 57 0.040
518
BRN004 Brain Edema 57 0.040
519
ADN027 Adenomyosis 57 0.040
520
ECH003 Echinococcosis 57 0.040
521
PLM010 Pulmonary Edema 57 0.040
522
DBN001 Dubin-Johnson Syndrome 56 0.040
523
PLV003 Pelvic Inflammatory Disease 56 0.040
524
MCN007 Meconium Aspiration Syndrome 55 0.040
525
P CRV031 Cervical Adenocarcinoma 55 0.040
526
P PMP001 Pemphigus 55 0.040
527
P PRT096 Peritoneal Mesothelioma 54 0.040
528
TST014 Testicular Cancer 54 0.040
529
RHM028 Rheumatic Heart Disease 54 0.040
530
P DBT005 Diabetes Insipidus 54 0.040
531
MCN001 Mucinous Adenocarcinoma 54 0.040
532
ASP003 Aseptic Meningitis 54 0.040
533
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 54 0.040
534
CRH005 Crohn's Colitis 53 0.040
535
END031 Endometrial Stromal Sarcoma 53 0.040
536
P OBS001 Obstructive Jaundice 53 0.040
537
P OVR046 Ovarian Cyst 52 0.040
538
ILT001 Ileitis 52 0.040
539
c HPT015 Hepatitis D 52 0.040
540
HPT082 Hepatic Adenomas, Familial 52 0.040
541
SPL004 Splenic Marginal Zone Lymphoma 52 0.040
542
P FNC043 Fanconi Anemia, Complementation Group E 52 0.040
543
P PRC012 Pericardial Effusion 52 0.040
544
VSC044 Visceral Myopathy 52 0.040
545
PLY131 Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes 51 0.040
546
GSG001 Gas Gangrene 51 0.040
547
c MLG002 Malignant Peritoneal Mesothelioma 51 0.040
548
HST009 Histiocytoma 51 0.040
549
P HMR005 Hemorrhoid 51 0.040
550
P END047 Endophthalmitis 51 0.040
551
PRS045 Prostatic Hypertrophy 51 0.040
552
FCL012 Facial Paralysis 50 0.040
553
PRN011 Pernicious Anemia 50 0.040
554
P APL006 Aplasia Cutis Congenita 50 0.040
555
P MYM013 Moyamoya Disease 1 50 0.040
556
MGC001 Megacolon 50 0.040
557
ALV002 Alveolar Echinococcosis 49 0.040
558
CRY004 Cryoglobulinemia 49 0.040
559
HYD002 Hydronephrosis 49 0.040
560
NCR007 Necrotizing Fasciitis 49 0.040
561
P SYR001 Syringomyelia 49 0.040
562
c MLG069 Malignant Hypertension 49 0.040
563
MNN009 Meningoencephalitis 49 0.040
564
SMN007 Seminoma 49 0.040
565
URT010 Ureteral Obstruction 49 0.040
566
P NNT009 Neonatal Diabetes Mellitus 48 0.040
567
P ENC008 Encephalocele 48 0.040
568
STS002 Situs Inversus 48 0.040
569
SCT005 Scott Syndrome 48 0.040
570
FBR019 Fibromatosis 47 0.040
571
ADR004 Adrenal Cortical Adenocarcinoma 47 0.040
572
LPD004 Lipoid Nephrosis 46 0.040
573
CRB004 Cerebral Artery Occlusion 46 0.040
574
NRR001 Neuroretinitis 46 0.040
575
c SVR056 Severe Hemophilia a 46 0.040
576
EVN001 Evans' Syndrome 45 0.040
577
MTR003 Mitral Valve Stenosis 45 0.040
578
LMY003 Leiomyomatosis 45 0.040
579
c ACQ042 Acquired Hemophilia a 44 0.040
580
TRN007 Transsexualism 44 0.040
581
ALX001 Alexia 44 0.040
582
HPT067 Hepatocellular Adenoma 43 0.040
583
HMN016 Hemangioendothelioma 43 0.040
584
ACN019 Acanthamoeba Keratitis 41 0.040
585
SCT001 Sciatic Neuropathy 41 0.040
586
c ALZ056 Alzheimer Disease 3 41 0.040
587
PLS029 Plasminogen Activator Inhibitor-1 Deficiency 41 0.040
588
STR077 Streptococcal Toxic-Shock Syndrome 40 0.040
589
CHP002 Chops Syndrome 40 0.040
590
BLR027 Blue Rubber Bleb Nevus 39 0.040
591
P MXL015 Maxillary Sinusitis 39 0.040
592
P ATM020 Autoimmune Enteropathy 39 0.040
593
PRL008 Paralytic Ileus 38 0.040
594
c SBC003 Subacute Bacterial Endocarditis 38 0.040
595
HPT008 Hepatic Tuberculosis 37 0.040
596
IMM064 Immunodeficiency, Common Variable, 10 37 0.040
597
PLX004 Plexopathy 37 0.040
598
LYM005 Lymphocele 37 0.040
599
OBS004 Obstructive Hydrocephalus 37 0.040
600
P GRM010 Germ Cells Tumors 37 0.040
601
P ANX007 Anauxetic Dysplasia 1 36 0.040
602
c ACT036 Acute Cholangitis 35 0.040
603
PLM052 Pulmonary Arteriovenous Malformation 35 0.040
604
PRN039 Paraneoplastic Syndromes 35 0.040
605
MLK004 Malakoplakia 34 0.040
606
ARG001 Argentine Hemorrhagic Fever 34 0.040
607
MNG003 Mungan Syndrome 34 0.040
608
MYS004 Myiasis 34 0.040
609
SPN331 Spondyloocular Syndrome 34 0.040
610
TXC001 Toxic Megacolon 34 0.040
611
LNG095 Lung Abscess 34 0.040
612
P BCT020 Bacteremia 2 34 0.040
613
MSN003 Mesenteric Vascular Occlusion 33 0.040
614
ANG066 Angel-Shaped Phalangoepiphyseal Dysplasia 33 0.040
615
ALP072 Alpha-Fetoprotein Deficiency 32 0.040
616
ANT022 Anterior Cranial Fossa Meningioma 32 0.040
617
LYM014 Lymphangitis 32 0.040
618
SBN001 Subendocardial Myocardial Infarction 31 0.040
619
VRT001 Vertebral Artery Occlusion 31 0.040
620
HNS001 Hansen's Disease 31 0.040
621
ART110 Arteritic Anterior Ischemic Optic Neuropathy 31 0.040
622
PRC051 Paracetamol Poisoning 30 0.040
623
OPT010 Optic Papillitis 30 0.040
624
PRM008 Parametritis 29 0.040
625
P RNG031 Ring Chromosome Y Syndrome 29 0.040
626
ABD002 Abducens Nerve Disease 28 0.040
627
c PST001 Posterior Myocardial Infarction 28 0.040
628
DNT046 Dental Abscess 28 0.040
629
FBR028 Fibrosing Mediastinitis 28 0.040
630
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 27 0.040
631
FBR052 Fibrinolytic Defect 26 0.040
632
NRS005 Neurosarcoidosis 26 0.040
633
PRT130 Protein Z Deficiency 25 0.040
634
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 24 0.040
635
TRN069 Transsexuality 23 0.040
636
CVR001 Cavernous Sinus Meningioma 23 0.040
637
SNG003 Single Ventricular Heart 23 0.040
638
ANS021 Anisocoria 22 0.040
639
c CHR036 Chronic Cholangitis 22 0.040
640
PRT112 Portal Hypertension, Noncirrhotic 21 0.040
641
c ACT035 Acute Frontal Sinusitis 21 0.040
642
CRN197 Coronary Arterial Fistulas 19 0.040
643
THR007 Thrombophlebitis Migrans 18 0.040
644
CRT056 Carotidynia 16 0.040
645
SVR099 Severe Hereditary Thrombophilia Due to Congenital Protein S Deficiency 15 0.040
646
OCL024 Ocular Neuromyotonia 14 0.040
647
P PRS040 Prostate Cancer 88 0.035
648
MLR004 Malaria 86 0.035
649
c HYP595 Hypertension, Essential 78 0.035
650
P DLT002 Dilated Cardiomyopathy 76 0.035
651
P WSK001 Wiskott-Aldrich Syndrome 76 0.035
652
ALP046 Alport Syndrome, X-Linked 74 0.035
653
GLB002 Glioblastoma 74 0.035
654
MYC006 Mycosis Fungoides 73 0.035
655
P FML018 Familial Mediterranean Fever 73 0.035
656
P NRB001 Neuroblastoma 73 0.035
657
PLM001 Pulmonary Tuberculosis 72 0.035
658
P CRV035 Cervical Cancer 72 0.035
659
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.035
660
FBR012 Fabry Disease 72 0.035
661
c CHR089 Chronic Kidney Failure 72 0.035
662
SVR004 Severe Combined Immunodeficiency 71 0.035
663
CRZ001 Crouzon Syndrome 71 0.035
664
P HRP006 Herpes Simplex 70 0.035
665
P TST021 Testicular Germ Cell Tumor 70 0.035
666
PTZ001 Peutz-Jeghers Syndrome 70 0.035
667
P DMN001 Diamond-Blackfan Anemia 70 0.035
668
GLB015 Glioblastoma Multiforme 68 0.035
669
P DYS007 Dyskeratosis Congenita 68 0.035
670
LYM007 Lymphangioleiomyomatosis 68 0.035
671
BRT054 Brittle Bone Disorder 67 0.035
672
P PRD006 Prader-Willi Syndrome 66 0.035
673
MXD005 Mixed Connective Tissue Disease 66 0.035
674
P PLY011 Polycystic Ovary Syndrome 65 0.035
675
P CLC063 Celiac Disease 1 65 0.035
676
LGN002 Legionellosis 65 0.035
677
P HYP061 Hypertrophic Cardiomyopathy 65 0.035
678
SCR008 Scrub Typhus 65 0.035
679
c ART101 Aortic Valve Disease 2 65 0.035
680
PRT010 Parathyroid Carcinoma 64 0.035
681
P MYS005 Myositis 63 0.035
682
P SPN046 Spinal Muscular Atrophy 63 0.035
683
P PLC011 Pilocytic Astrocytoma 63 0.035
684
P HRM001 Hermansky-Pudlak Syndrome 62 0.035
685
P PRP029 Porphyria 62 0.035
686
LSC001 Lesch-Nyhan Syndrome 62 0.035
687
P ACT074 Acute Lymphocytic Leukemia 61 0.035
688
P UVT001 Uveitis 61 0.035
689
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.035
690
QFV001 Q Fever 61 0.035
691
P GST044 Gastritis 61 0.035
692
HRP004 Herpes Zoster 61 0.035
693
P NTR004 Neutropenia 60 0.035
694
STT001 Status Epilepticus 60 0.035
695
NTH001 Netherton Syndrome 60 0.035
696
JNT002 Joint Disorders 60 0.035
697
CCC001 Coccidioidomycosis 60 0.035
698
GST040 Gastric Adenocarcinoma 60 0.035
699
P FCL005 Focal Segmental Glomerulosclerosis 60 0.035
700
MLG077 Malignant Peripheral Nerve Sheath Tumor 59 0.035
701
JPN002 Japanese Encephalitis 59 0.035
702
P VNT002 Ventricular Septal Defect 59 0.035
703
ING001 Inguinal Hernia 59 0.035
704
P OLG002 Oligodendroglioma 59 0.035
705
TRN015 Transient Cerebral Ischemia 58 0.035
706
APH002 Aphasia 58 0.035
707
SFT003 Soft Tissue Sarcoma 58 0.035
708
LMY002 Leiomyoma 58 0.035
709
CRT002 Cartilage-Hair Hypoplasia 58 0.035
710
CMP010 Complex Regional Pain Syndrome 58 0.035
711
NRN004 Neuroendocrine Tumor 58 0.035
712
HMT018 Hematopoietic Stem Cell Transplantation 58 0.035
713
P PLY006 Polydactyly 57 0.035
714
UTR024 Uterine Carcinosarcoma 57 0.035
715
P MCR010 Microcephaly 57 0.035
716
VND007 Van Der Woude Syndrome 1 57 0.035
717
GST023 Gastric Ulcer 57 0.035
718
P ANG015 Angioedema 57 0.035
719
ERD001 Erdheim-Chester Disease 57 0.035
720
CYS005 Cysticercosis 57 0.035
721
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 57 0.035
722
CHL014 Cholera 56 0.035
723
c ANM038 Anemia, Autoimmune Hemolytic 56 0.035
724
c ALM001 Al Amyloidosis 56 0.035
725
P SCL018 Scoliosis 56 0.035
726
P CHN012 Chondrosarcoma 56 0.035
727
P EHL052 Ehlers-Danlos Syndrome, Vascular Type 56 0.035
728
P OST135 Osteogenesis Imperfecta, Type I 56 0.035
729
P PMP005 Pemphigus Vulgaris 56 0.035
730
ANK001 Ankylosis 56 0.035
731
CRT049 Critical Limb Ischemia 56 0.035
732
GST037 Gastroparesis 56 0.035
733
GST009 Gastroschisis 55 0.035
734
P MSC003 Muscular Atrophy 55 0.035
735
HPT022 Hepatoblastoma 55 0.035
736
STR020 Strabismus 55 0.035
737
AMN001 Amenorrhea 55 0.035
738
MGR028 Migraine with or Without Aura 1 55 0.035
739
SRS001 Serous Cystadenocarcinoma 55 0.035
740
P SYP003 Syphilis 55 0.035
741
P SZR006 Seizure Disorder 55 0.035
742
SPR004 Supravalvular Aortic Stenosis 54 0.035
743
c INF071 Inflammatory Bowel Disease 1 54 0.035
744
TBR011 Tuberculous Meningitis 54 0.035
745
CCT002 Cicatricial Pemphigoid 54 0.035
746
MYL020 Myelomeningocele 54 0.035
747
MCR004 Macroglobulinemia 54 0.035
748
QDR001 Quadriplegia 54 0.035
749
ART001 Arterial Tortuosity Syndrome 53 0.035
750
CLC001 Calciphylaxis 53 0.035
751
GTR002 Goiter 53 0.035
752
P CLL015 Collagen Disease 53 0.035
753
LGN001 Legionnaires' Disease 53 0.035
754
P PRM002 Primary Hyperoxaluria 53 0.035
755
LPR001 Lepromatous Leprosy 53 0.035
756
P CTN003 Cutaneous Lupus Erythematosus 53 0.035
757
P TRN034 Transverse Myelitis 53 0.035
758
ERY008 Erythromelalgia 53 0.035
759
P TRT010 Teratoma 53 0.035
760
CLN015 Colon Adenocarcinoma 53 0.035
761
ALC009 Alcoholic Liver Cirrhosis 53 0.035
762
P PNV001 Panuveitis 52 0.035
763
c PNS012 Paine Syndrome 52 0.035
764
GRW007 Growth Hormone Deficiency 52 0.035
765
EXT010 Extramedullary Plasmacytoma 52 0.035
766
TLN003 Telangiectasis 52 0.035
767
MTN003 Motion Sickness 52 0.035
768
P RNL007 Renal Tubular Acidosis 51 0.035
769
P ACT150 Acute Adrenal Insufficiency 51 0.035
770
RFL001 Reflex Sympathetic Dystrophy 51 0.035
771
P RST002 Restrictive Cardiomyopathy 51 0.035
772
c INV001 Invasive Aspergillosis 51 0.035
773
P ATR005 Atrophic Gastritis 51 0.035
774
CRN027 Corneal Neovascularization 51 0.035
775
INT067 Interstitial Nephritis 51 0.035
776
CYS014 Cystadenocarcinoma 51 0.035
777
PRT029 Parathyroid Adenoma 50 0.035
778
CHL061 Childhood Leukemia 50 0.035
779
WHP001 Whipple Disease 50 0.035
780
P PTS002 Ptosis 50 0.035
781
LYM012 Lymphoplasmacytic Lymphoma 50 0.035
782
JCB001 Jacobsen Syndrome 50 0.035
783
P EPT020 Epithelioid Hemangioendothelioma 50 0.035
784
RNL024 Renal Glucosuria 50 0.035
785
c PST005 Posterior Uveitis 50 0.035
786
RNL011 Renal Osteodystrophy 49 0.035
787
TRN044 Transposition of the Great Arteries 49 0.035
788
DFF036 Differentiated Thyroid Carcinoma 49 0.035
789
PNC119 Pancreatic Neuroendocrine Tumor 49 0.035
790
ERY029 Erythermalgia, Primary 48 0.035
791
KMR001 Kimura Disease 48 0.035
792
HNC001 Henoch-Schoenlein Purpura 48 0.035
793
PNN001 Panniculitis 48 0.035
794
CVR006 Cavernous Hemangioma 48 0.035
795
P SDR002 Siderosis 48 0.035
796
P VGN017 Vaginal Cancer 48 0.035
797
ART004 Aortic Atherosclerosis 48 0.035
798
RFR010 Refractory Anemia 48 0.035
799
CHR008 Choroiditis 47 0.035
800
c BRN108 Branchiootic Syndrome 1 47 0.035
801
P CLS010 Cluster Headache 47 0.035
802
SGN002 Signet Ring Cell Adenocarcinoma 47 0.035
803
P PSD003 Pseudohypoaldosteronism 47 0.035
804
PST011 Pustulosis of Palm and Sole 47 0.035
805
RTN001 Retinal Vasculitis 47 0.035
806
PLR005 Pleuropneumonia 47 0.035
807
P ATX024 Ataxia-Oculomotor Apraxia 3 47 0.035
808
TBR006 Tuberculoid Leprosy 46 0.035
809
TBR008 Tuberculous Peritonitis 46 0.035
810
NPH010 Nephrosclerosis 46 0.035
811
PLC001 Placenta Accreta 46 0.035
812
END020 Endocardial Fibroelastosis 46 0.035
813
FBR003 Fibrous Histiocytoma 46 0.035
814
HRT012 Heart Valve Disease 45 0.035
815
HST016 Histiocytic Sarcoma 45 0.035
816
P CHR342 Chiari Malformation 45 0.035
817
c ART061 Arthrogryposis, Distal, Type 2a 45 0.035
818
P PRT026 Parotitis 45 0.035
819
CNT060 Central Serous Chorioretinopathy 45 0.035
820
BRK001 Brooke-Spiegler Syndrome 45 0.035
821
BRN014 Bronchopneumonia 45 0.035
822
c ACQ012 Acquired Angioedema 45 0.035
823
INT071 Intestinal Perforation 44 0.035
824
GLC096 Galactorrhea 44 0.035
825
DVR002 Diverticulitis 44 0.035
826
c WLM011 Wilms Tumor 6 44 0.035
827
NRS003 Neurosyphilis 44 0.035
828
QBC001 Quebec Platelet Disorder 44 0.035
829
CYS009 Cystadenoma 44 0.035
830
ASP030 Aspirin Resistance 44 0.035
831
CLL002 Collecting Duct Carcinoma 43 0.035
832
CHR034 Chromophobe Adenoma 43 0.035
833
VNW008 Von Willebrand Disease, Type 3 43 0.035
834
ILC002 Ileocolitis 43 0.035
835
GNT031 Genitopatellar Syndrome 43 0.035
836
P BRN035 Brain Stem Glioma 42 0.035
837
IDP070 Idiopathic Scoliosis 42 0.035
838
MTS001 Mutism 42 0.035
839
CRT008 Carotid Artery Dissection 42 0.035
840
CNV002 Conversion Disorder 42 0.035
841
SPL012 Splenic Disease 42 0.035
842
MNN017 Mononeuropathy 42 0.035
843
BRS064 Bursitis 42 0.035
844
PRG008 Paragonimiasis 42 0.035
845
SPR007 Superior Mesenteric Artery Syndrome 42 0.035
846
INT060 Intestinal Atresia 42 0.035
847
P CNG048 Congenital Hepatic Fibrosis 41 0.035
848
P HRD012 Hereditary Elliptocytosis 41 0.035
849
ADN002 Adenoiditis 40 0.035
850
P HYP265 Hypotonia 40 0.035
851
GST071 Gastrointestinal Carcinoma 40 0.035
852
ALP043 Alpha-2-Plasmin Inhibitor Deficiency 40 0.035
853
SPR066 Superficial Siderosis 40 0.035
854
WLL004 Wallerian Degeneration 40 0.035
855
INT042 Internuclear Ophthalmoplegia 40 0.035
856
WBR001 Weber Syndrome 40 0.035
857
c CNT028 Central Retinal Artery Occlusion 40 0.035
858
ACQ017 Acquired Von Willebrand Syndrome 40 0.035
859
CNG069 Congenital Cytomegalovirus 40 0.035
860
c HMG001 Hemoglobin C Disease 39 0.035
861
ACL001 Acalculous Cholecystitis 39 0.035
862
ALC005 Alcoholic Pancreatitis 39 0.035
863
c PSR018 Psoriasis 13 39 0.035
864
INP001 Inappropriate Adh Syndrome 39 0.035
865
GLC008 Glucose Metabolism Disease 38 0.035
866
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.035
867
MLG086 Malignant Hyperthermia Susceptibility 38 0.035
868
AGR018 Agraphia 38 0.035
869
P CRB088 Cerebral Atrophy 38 0.035
870
MSN002 Mesenteric Lymphadenitis 38 0.035
871
P MNN007 Meningocele 38 0.035
872
GLS018 Glass Syndrome 38 0.035
873
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 38 0.035
874
MLN013 Melanoma Metastasis 37 0.035
875
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 37 0.035
876
AMR003 Amaurosis Fugax 37 0.035
877
BHR001 Behr Syndrome 36 0.035
878
ANG017 Angiolipoma 36 0.035
879
GPS001 Gapo Syndrome 36 0.035
880
BRN118 Brain Small Vessel Disease with or Without Ocular Anomalies 36 0.035
881
LYM011 Lymphogranuloma Venereum 36 0.035
882
TST043 Testicular Seminoma 36 0.035
883
VSC008 Vascular Hemostatic Disease 36 0.035
884
AMP007 Amphetamine Abuse 36 0.035
885
PLY024 Polymicrogyria 36 0.035
886
UTR020 Uterine Inversion 36 0.035
887
HYP015 Hyperlucent Lung 36 0.035
888
PRC010 Pericardial Mesothelioma 35 0.035
889
GST016 Gastric Signet Ring Cell Adenocarcinoma 35 0.035
890
P CMM008 Communicating Hydrocephalus 35 0.035
891
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 35 0.035
892
HRS011 Horseshoe Kidney 35 0.035
893
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 35 0.035
894
LGN006 Legionnaire Disease 35 0.035
895
VTM001 Vitamin K Deficiency Hemorrhagic Disease 35 0.035
896
FTD001 Foot Drop 35 0.035
897
HYP034 Hypertensive Encephalopathy 34 0.035
898
ETH009 Ethmoid Sinusitis 34 0.035
899
PRN007 Perinephritis 34 0.035
900
CRD016 Cardiac Rupture 34 0.035
901
INT020 Intravenous Leiomyomatosis 34 0.035
902
CHR076 Choriocarcinoma of the Testis 33 0.035
903
c INF145 Infantile Liver Failure Syndrome 1 33 0.035
904
MYS001 Myositis Ossificans 33 0.035
905
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 33 0.035
906
c MLT009 Multiple Cranial Nerve Palsy 33 0.035
907
ULN001 Ulnar Neuropathy 33 0.035
908
ART012 Aortitis 33 0.035
909
GND003 Gonadal Disease 32 0.035
910
XNT001 Xanthogranulomatous Pyelonephritis 32 0.035
911
ALC001 Alcohol-Related Birth Defect 32 0.035
912
MTL005 Metal Allergy 32 0.035
913
SCR024 Sacrococcygeal Teratoma 32 0.035
914
RNL001 Renal Artery Obstruction 31 0.035
915
SBC014 Subclavian Steal Syndrome 31 0.035
916
BRW004 Brown-Sequard Syndrome 30 0.035
917
RCT008 Rectosigmoid Junction Neoplasm 30 0.035
918
HMN004 Hemangioma of Liver 30 0.035
919
RHS001 Rh Isoimmunization 30 0.035
920
SBS006 Sebastian Syndrome 30 0.035
921
SPL007 Splenic Abscess 29 0.035
922
UNV002 Univentricular Heart 29 0.035
923
P DCR004 Dacryocystitis 29 0.035
924
PMP008 Pemphigus Vegetans 29 0.035
925
PLM058 Pulmonary Atresia with Intact Ventricular Septum 29 0.035
926
SVN002 Sveinsson Chorioretinal Atrophy 29 0.035
927
DSC004 Discitis 28 0.035
928
MDN008 Median Arcuate Ligament Syndrome 28 0.035
929
BRN055 Bronchogenic Cyst 28 0.035
930
FBR089 Fibrosclerosis, Multifocal 28 0.035
931
CNG134 Congenitally Corrected Transposition of the Great Arteries 28 0.035
932
PRT086 Partial Hydatidiform Mole 28 0.035
933
RVR002 Reversible Cerebral Vasoconstriction Syndrome 27 0.035
934
PRL014 Paralytic Squint 27 0.035
935
BLD052 Blood Group Incompatibility 26 0.035
936
BNM005 Bone Marrow Necrosis 26 0.035
937
PRF003 Piriformis Syndrome 26 0.035
938
HMX003 Heme Oxygenase 1 Deficiency 26 0.035
939
HMC012 Hemicrania Continua 26 0.035
940
c TST046 Testicular Germ Cell Tumor 1 26 0.035
941
SPR032 Superficial Siderosis of the Central Nervous System 25 0.035
942
SBS002 Substernal Goiter 25 0.035
943
c PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 25 0.035
944
CRT028 Cor Triatriatum 25 0.035
945
CRB017 Cerebral Falx Meningioma 25 0.035
946
MDD005 Middle Lobe Syndrome 24 0.035
947
MYX006 Myxoid Leiomyosarcoma 24 0.035
948
SBC002 Subclavian Artery Aneurysm 23 0.035
949
MNS002 Mini Stroke 23 0.035
950
CHR158 Charles Bonnet Syndrome 23 0.035
951
MXD035 Mixed-Type Autoimmune Hemolytic Anemia 22 0.035
952
c ADM010 Adams-Oliver Syndrome 5 22 0.035
953
STN013 Stenotrophomonas Maltophilia Infection 22 0.035
954
CCN009 Cocaine Intoxication 22 0.035
955
P ACT232 Acute Necrotizing Encephalopathy 21 0.035
956
PGM028 Pigmented Purpuric Dermatosis 21 0.035
957
HPT066 Hepatoportal Sclerosis 20 0.035
958
PPL054 Popliteal Cyst 20 0.035
959
AMN015 Amenorrhea-Galactorrhea Syndrome 20 0.035
960
CNG298 Congenital Pancreatic Cyst 20 0.035
961
CNT067 Central Cord Syndrome 19 0.035
962
DBL004 Double Discordia 19 0.035
963
BNT001 Banti's Syndrome 19 0.035
964
FXL001 Foix-Alajouanine Syndrome 18 0.035
965
PNT023 Pontine Hemorrhage 18 0.035
966
PLS001 Pulsating Exophthalmos 18 0.035
967
CNG171 Congenital Plasminogen Deficiency 17 0.035
968
CGH002 Cough Headache 17 0.035
969
HMN038 Human Coronavirus Sensitivity 17 0.035
970
INT055 Intravascular Fasciitis 17 0.035
971
ART109 Arterial Thoracic Outlet Syndrome 16 0.035
972
CNG092 Congenital Extrahepatic Portosystemic Shunt 15 0.035
973
FCT013 Factor V Leiden Thrombophilia 15 0.035
974
MND006 Mondor Disease 15 0.035
975
TMP006 Temporomandibular Ankylosis 15 0.035
976
PLM062 Pulmonary Hyalinizing Granuloma 14 0.035
977
BRS103 Bier Spots 14 0.035
978
DRL001 Dural Sinus Malformation 14 0.035
979
CYS035 Cystic Adventitial Disease 13 0.035
980
P HYP607 Hypercholesterolemia, Familial 81 0.029
981
c LKM063 Leukemia, Chronic Myeloid 80 0.029
982
c LKM071 Leukemia, Chronic Lymphocytic 75 0.029
983
CNN003 Conn's Syndrome 70 0.029
984
c MNN043 Meningioma, Familial 69 0.029
985
APN008 Apnea, Obstructive Sleep 67 0.029
986
ADL030 Adult-Onset Still's Disease 65 0.029
987
c MCP049 Mucopolysaccharidosis, Type Vii 64 0.029
988
END030 End Stage Renal Failure 59 0.029
989
LPD008 Lipid Metabolism Disorder 59 0.029
990
STR039 Sturge-Weber Syndrome 59 0.029
991
P OVR049 Ovarian Disease 58 0.029
992
HNT002 Hantavirus Pulmonary Syndrome 57 0.029
993
RTN018 Retinal Disease 56 0.029
994
HYP060 Hyperinsulinism 56 0.029
995
IGR001 Ige Responsiveness, Atopic 56 0.029
996
ACR008 Acrocallosal Syndrome 56 0.029
997
P CNG411 Congenital Disorder of Glycosylation, Type in 55 0.029
998
ARS001 Aarskog-Scott Syndrome 55 0.029
999
ENC044 Enchondromatosis, Multiple, Ollier Type 54 0.029
1000
c CLR131 Ciliary Dyskinesia, Primary, 1 54 0.029
1001
P TRC086 Trichohepatoenteric Syndrome 1 54 0.029
1002
DNY001 Denys-Drash Syndrome 54 0.029
1003
P SCH018 Schizencephaly 53 0.029
1004
P CRD132 Cardiac Conduction Defect 53 0.029
1005
CRT013 Carotid Stenosis 52 0.029
1006
BBS001 Babesiosis 51 0.029
1007
RPP001 Rapp-Hodgkin Syndrome 51 0.029
1008
HMR002 Hemarthrosis 51 0.029
1009
MLT145 Multiple Enchondromatosis, Maffucci Type 51 0.029
1010
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 51 0.029
1011
ANX004 Anoxia 49 0.029
1012
AND020 Androgen Insensitivity, Partial 49 0.029
1013
PRM020 Premenstrual Tension 49 0.029
1014
RYN001 Raynaud Disease 48 0.029
1015
DBT008 Diabetic Angiopathy 48 0.029
1016
c AMY009 Amyloidosis Aa 48 0.029
1017
CHL128 Childhood Hepatocellular Carcinoma 47 0.029
1018
KLT001 Klatskin's Tumor 47 0.029
1019
VLP002 Valproate Embryopathy 46 0.029
1020
c MTR002 Mitral Valve Insufficiency 46 0.029
1021
GLC011 Galactose Epimerase Deficiency 46 0.029
1022
ENH001 Enhanced S-Cone Syndrome 46 0.029
1023
P HRN001 Horner's Syndrome 45 0.029
1024
P ANL018 Analbuminemia 45 0.029
1025
P ATR010 Atrial Heart Septal Defect 45 0.029
1026
PRN037 Prinzmetal's Variant Angina 44 0.029
1027
ACT058 Active Peptic Ulcer Disease 43 0.029
1028
CRB108 Cerebral Palsy, Ataxic, Autosomal Recessive 43 0.029
1029
ACT088 Acute Insulin Response 43 0.029
1030
ENC039 Encephalopathy, Familial, with Neuroserpin Inclusion Bodies 42 0.029
1031
c CNG208 Congenital Disorder of Glycosylation, Type Iic 42 0.029
1032
GNT050 Genitourinary Tract Anomalies 41 0.029
1033
MYH012 Myhre Syndrome 41 0.029
1034
P CHR084 Chromosomal Disease 40 0.029
1035
ORB013 Orbital Disease 40 0.029
1036
c HYP793 Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 40 0.029
1037
FMR003 Femoral Neuropathy 39 0.029
1038
CPL013 Capillary Malformations, Congenital 39 0.029
1039
MHR001 Mohr-Tranebjaerg Syndrome 39 0.029
1040
SQM002 Squamous Cell Papilloma 39 0.029
1041
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 39 0.029
1042
c LPD019 Lipodystrophy, Partial, Acquired 38 0.029
1043
MLN073 Melanosis, Neurocutaneous 38 0.029
1044
c LKD009 Leukodystrophy, Hypomyelinating, 5 38 0.029
1045
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.029
1046
SXD001 Sex Differentiation Disease 37 0.029
1047
c LKM004 Leukemia, B-Cell, Chronic 37 0.029
1048
c CNG189 Congenital Disorder of Glycosylation, Type Ib 36 0.029
1049
ATR013 Atrichia with Papular Lesions 36 0.029
1050
FNT004 Fainting 36 0.029
1051
PLM013 Pulmonary Immaturity 36 0.029
1052
DYS013 Dysbaric Osteonecrosis 35 0.029
1053
CHR178 Chromosomal Triplication 35 0.029
1054
c LKM056 Leukemia, Chronic Lymphocytic 2 35 0.029
1055
c CNG379 Congenital Disorder of Glycosylation, Type It 34 0.029
1056
HMP001 Hemopericardium 34 0.029
1057
c DNR003 Duane Retraction Syndrome 1 34 0.029
1058
ACT056 Acute Cor Pulmonale 34 0.029
1059
PSD048 Pseudo-Von Willebrand Disease 33 0.029
1060
PLS030 Plasminogen Deficiency, Type I 33 0.029
1061
c ACQ010 Acquired Polycythemia 33 0.029
1062
49X002 49,xxxxy Syndrome 33 0.029
1063
DHY016 Dehydrated Hereditary Stomatocytosis 1 with or Without Pseudohyperkalemia and/or Perinatal Edema 32 0.029
1064
BRK012 Broken Heart Syndrome 31 0.029
1065
P MLD013 Mild Hemophilia a 30 0.029
1066
ATM052 Autoimmune Disease 1 30 0.029
1067
FCL084 Facial Dysmorphism, Immunodeficiency, Livedo, and Short Stature 30 0.029
1068
c SRC023 Sarcoidosis 2 30 0.029
1069
CRN048 Craniofacial-Deafness-Hand Syndrome 29 0.029
1070
DVL012 Developmental Dysplasia of the Hip 1 27 0.029
1071
CRN270 Coronary Artery Dissection, Spontaneous 27 0.029
1072
c ANG045 Angioedema, Hereditary, Type Iii 26 0.029
1073
ANG062 Angioosteohypertrophic Syndrome 25 0.029
1074
TMP008 Tempi Syndrome 25 0.029
1075
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 25 0.029
1076
RMR001 Ramer Ladda Syndrome 24 0.029
1077
P ACT080 Acute Pulmonary Heart Disease 24 0.029
1078
c LYM128 Lymphedema, Hereditary, Iii 24 0.029
1079
STB002 Satb2-Associated Syndrome 24 0.029
1080
ACR079 Acrodysostosis with Multiple Hormone Resistance 24 0.029
1081
END074 Endocardium Disease 22 0.029
1082
CRD023 Cardiomyopathy Cataract Hip Spine Disease 21 0.029
1083
DSS003 Disseminated Eosinophilic Collagen Disease 20 0.029
1084
DFF027 Diffuse Lymphatic Malformation 19 0.029
1085
48X002 48,xxxy Syndrome 19 0.029
1086
c PRX094 Paroxysmal Nocturnal Hemoglobinuria 1 19 0.029
1087
MSC148 Musical Perfect Pitch 19 0.029
1088
THR120 Thrombophilia Due to Histidine-Rich Glycoprotein Deficiency 17 0.029
1089
HMC030 Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency 17 0.029
1090
IMM162 Immunoglobulin E Concentration, Serum 16 0.029
1091
LRY021 Laryngeal Adductor Paralysis 15 0.029
1092
FNC050 Functioning Gonadotropic Adenoma 15 0.029
1093
P ACT077 Acute Orbital Inflammation 15 0.029
1094
CYT018 Cytochrome P450 2d6 Variant 13 0.029
1095
BLT017 Bilateral Massive Adrenal Hemorrhage 13 0.029
1096
PRT045 Prothrombin-Related Thrombophilia 12 0.029
1097
ACT174 Acute Peripheral Arterial Occlusion 11 0.029
1098
c EST011 Esterase C 10 0.029
1099
P ALZ034 Alzheimer Disease 95 0.020
1100
OST012 Osteoarthritis 88 0.020
1101
P RTT002 Rett Syndrome 82 0.020
1102
P RTN008 Retinitis Pigmentosa 81 0.020
1103
P FNC027 Fanconi Anemia, Complementation Group a 78 0.020
1104
LYM133 Lymphoma, Hodgkin, Classic 78 0.020
1105
P NRV007 Nervous System Disease 75 0.020
1106
MSC157 Muscular Dystrophy, Duchenne Type 74 0.020
1107
ANX010 Anxiety 72 0.020
1108
LYM143 Lymphoma, Non-Hodgkin, Familial 71 0.020
1109
CNR004 Cone-Rod Dystrophy 2 69 0.020
1110
P DRM053 Dermatitis, Atopic 68 0.020
1111
c PRM196 Premature Ovarian Failure 1 68 0.020
1112
SKN016 Skin Disease 68 0.020
1113
c SML038 Small Cell Cancer of the Lung 67 0.020
1114
HSH003 Hashimoto Thyroiditis 67 0.020
1115
DNG002 Dengue Hemorrhagic Fever 66 0.020
1116
P MCR115 Microvascular Complications of Diabetes 5 66 0.020
1117
TKY002 Takayasu Arteritis 66 0.020
1118
c DNG003 Dengue Disease 66 0.020
1119
GST045 Gastroenteritis 65 0.020
1120
ACR006 Aceruloplasminemia 65 0.020
1121
c CNT035 Central Nervous System Disease 65 0.020
1122
P ART067 Aortic Aneurysm, Familial Thoracic 1 65 0.020
1123
CNT097 Central Hypoventilation Syndrome, Congenital 65 0.020
1124
VRL011 Viral Infectious Disease 64 0.020
1125
MSC152 Muscular Dystrophy, Becker Type 64 0.020
1126
HMT002 Hematologic Cancer 64 0.020
1127
IMM174 Immunodeficiency with Hyper-Igm, Type 1 64 0.020
1128
CMB081 Combined Immunodeficiency, X-Linked 64 0.020
1129
LNG108 Langerhans Cell Histiocytosis 63 0.020
1130
PNC033 Pancreas Adenocarcinoma 63 0.020
1131