Search results for "thrombosis"

The MalaCard for "thrombosis" has been retired.
Searching MalaCards for entries containing "thrombosis"

1434 hits were found for 'thrombosis'

# Family MCID Name MIFTS Score
1
SGT001 Sagittal Sinus Thrombosis 32 5.806
2
PRT018 Portal Vein Thrombosis 48 5.544
3
c THR092 Thrombophilia Due to Thrombin Defect 56 5.481
4
CRN017 Coronary Thrombosis 46 5.471
5
LTR002 Lateral Sinus Thrombosis 25 5.030
6
CVR002 Cavernous Sinus Thrombosis 28 4.748
7
CRT004 Carotid Artery Thrombosis 38 4.578
8
INT076 Intracranial Sinus Thrombosis 22 3.875
9
HPT002 Hepatic Vein Thrombosis 38 3.618
10
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 17 3.306
11
CRB132 Cerebral Sinovenous Thrombosis 30 2.222
12
P BDD001 Budd-Chiari Syndrome 52 2.173
13
FCT013 Factor V Leiden Thrombophilia 20 1.944
14
HMC020 Homocystinuria, B6-Responsive and Nonresponsive Types 29 1.935
15
THR055 Thrombophilia, X-Linked, Due to Factor Ix Defect 17 1.925
16
VNS012 Venous Thoracic Outlet Syndrome 15 1.913
17
CRB009 Cerebritis 36 0.452
18
PLM033 Pulmonary Embolism 59 0.274
19
VND001 Vein Disease 51 0.264
20
P MYC007 Myocardial Infarction 80 0.243
21
P THR015 Thrombophilia 59 0.235
22
P HPT021 Hepatitis 74 0.233
23
PRT014 Protein S Deficiency 54 0.232
24
P THR014 Thrombocytopenia 63 0.220
25
HPR003 Heparin-Induced Thrombocytopenia 45 0.212
26
PRT011 Protein C Deficiency 52 0.200
27
P ANT006 Antiphospholipid Syndrome 60 0.199
28
HPT023 Hepatocellular Carcinoma 90 0.181
29
ANR040 Aneurysm 56 0.180
30
c BLD124 Bleeding Disorder, Platelet-Type, 11 37 0.162
31
END072 Endotheliitis 41 0.156
32
c SYS001 Systemic Lupus Erythematosus 87 0.155
33
P ESS003 Essential Thrombocythemia 66 0.152
34
P LPS004 Lupus Erythematosus 63 0.150
35
HYP037 Hyperhomocysteinemia 49 0.150
36
P NPH012 Nephrotic Syndrome 55 0.145
37
PST095 Post-Thrombotic Syndrome 48 0.143
38
c ACT075 Acute Myocardial Infarction 61 0.141
39
LVR012 Liver Cirrhosis 71 0.138
40
P LKM002 Leukemia 70 0.137
41
P PNC044 Pancreatitis 62 0.129
42
VSC007 Vascular Disease 51 0.127
43
P PLY018 Polycythemia 58 0.127
44
CLT003 Colitis 56 0.127
45
ART111 Artery Disease 56 0.127
46
ULC004 Ulcerative Colitis 74 0.121
47
VSC006 Vascular Cancer 51 0.121
48
HDC001 Headache 52 0.121
49
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 59 0.119
50
PRP027 Peripheral Vascular Disease 69 0.119
51
P PRT013 Portal Hypertension 61 0.119
52
HMG002 Hemoglobinuria 49 0.119
53
THR016 Thrombophlebitis 55 0.118
54
ATH003 Atherosclerosis 63 0.117
55
ISC004 Ischemia 56 0.114
56
P SNS014 Sinusitis 66 0.112
57
BLD053 Blood Platelet Disease 44 0.112
58
P CRN211 Coronary Artery Disease 74 0.110
59
P LVR013 Liver Disease 76 0.110
60
P BLD051 Blood Coagulation Disease 44 0.110
61
P MNN013 Meningitis 66 0.109
62
VSC008 Vascular Hemostatic Disease 30 0.109
63
THR004 Thrombocytosis 55 0.104
64
MST019 Mastoiditis 31 0.104
65
HPT020 Hepatic Vascular Disease 43 0.104
66
DSS009 Disseminated Intravascular Coagulation 52 0.102
67
OTT002 Otitis Media 66 0.100
68
P LYM118 Lymphoma 68 0.097
69
PRP030 Purpura 60 0.097
70
P HYP098 Hypereosinophilic Syndrome 48 0.097
71
RTN023 Retinitis 49 0.097
72
INT003 Intracranial Hypotension 36 0.095
73
HDN002 Head Injury 47 0.095
74
P HMC002 Homocystinuria 52 0.093
75
P ART084 Arteriovenous Fistula 40 0.093
76
P HRT032 Heart Disease 64 0.091
77
CLL003 Cellulitis 49 0.091
78
INT075 Intracranial Hypertension 52 0.091
79
STR067 Stroke, Ischemic 74 0.090
80
P ADN016 Adenocarcinoma 69 0.088
81
P VNS003 Venous Insufficiency 53 0.088
82
TBR010 Tuberculosis 70 0.086
83
c CNG401 Congenital Heart Disease 67 0.086
84
OVR029 Ovarian Hyperstimulation Syndrome 59 0.086
85
SPN340 Spontaneous Intracranial Hypotension 22 0.083
86
P ENC018 Encephalopathy 59 0.079
87
ART021 Arteriosclerosis 59 0.079
88
c ACT027 Acute Pancreatitis 59 0.079
89
c MYC058 Myocardial Infarction 2 28 0.079
90
P LYM026 Lymphoblastic Leukemia 60 0.077
91
c CRN214 Coronary Heart Disease 5 22 0.077
92
ADJ001 Adjustment Disorder 38 0.077
93
CRN006 Coronary Aneurysm 31 0.077
94
PPL021 Papilledema 47 0.075
95
MYM001 Myoma 51 0.075
96
ANG054 Angina Pectoris 48 0.075
97
P OBS005 Obesity 91 0.072
98
P PLM037 Pulmonary Hypertension 78 0.072
99
CRH001 Crohn's Disease 76 0.072
100
DFC004 Deficiency Anemia 64 0.072
101
P MYL005 Myelofibrosis 67 0.072
102
IRN001 Iron Deficiency Anemia 51 0.072
103
P DYS026 Dysfibrinogenemia 36 0.072
104
CRD137 Cardiogenic Shock 44 0.072
105
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 27 0.070
106
P CRN178 Coronary Heart Disease 6 22 0.070
107
ALR002 Al-Raqad Syndrome 36 0.070
108
SPL006 Splenic Infarction 32 0.070
109
ISC006 Ischemic Heart Disease 54 0.070
110
P RNL014 Renal Cell Carcinoma 80 0.067
111
CSY001 C Syndrome 49 0.067
112
FCT004 Factor Xii Deficiency 51 0.067
113
THR013 Thoracic Outlet Syndrome 48 0.067
114
P HMP007 Hemophilia 55 0.067
115
LMR001 Lemierre's Syndrome 43 0.067
116
SPR035 Superior Vena Cava Syndrome 31 0.067
117
ORB006 Orbital Cellulitis 27 0.067
118
c CRN175 Coronary Heart Disease 4 19 0.067
119
P ATR011 Atrial Fibrillation 63 0.065
120
P MYL006 Myeloid Leukemia 67 0.065
121
VSC011 Vasculitis 62 0.065
122
P GLM007 Glomerulonephritis 56 0.065
123
CYT008 Cytomegalovirus Infection 51 0.065
124
CRT015 Carotid Artery Occlusion 43 0.065
125
P HYD006 Hydrocephalus 68 0.062
126
PRT036 Peritonitis 65 0.062
127
PTN001 Patent Foramen Ovale 55 0.062
128
P SPS003 Spastic Diplegia 49 0.062
129
SCK005 Sickle Cell Disease 51 0.062
130
P CRV039 Cervicitis 45 0.062
131
P OST028 Osteochondroma 45 0.062
132
c INF071 Inflammatory Bowel Disease 1 51 0.059
133
KWS002 Kawasaki Disease 70 0.059
134
CRB039 Cerebrovascular Disease 49 0.059
135
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.059
136
CHL067 Cholecystitis 57 0.059
137
ART005 Arteriovenous Malformation 63 0.059
138
ATR060 Atrial Standstill, Digenic 51 0.059
139
HPT019 Hepatic Encephalopathy 58 0.059
140
P HYP083 Hypopituitarism 50 0.059
141
P INT030 Intracranial Aneurysm 52 0.059
142
SPP008 Suppurative Otitis Media 45 0.059
143
HRT012 Heart Valve Disease 39 0.059
144
MMB002 Membranous Glomerulonephritis 47 0.059
145
P CRN074 Coronary Artery Aneurysm 44 0.059
146
SPH007 Sphenoid Sinusitis 23 0.059
147
c CRN174 Coronary Heart Disease 2 19 0.059
148
CRB085 Cerebral Hemorrhage 40 0.059
149
VSC047 Vascular Malformation 45 0.059
150
PLY125 Polycythemia Vera, Somatic 63 0.056
151
ART016 Aortic Aneurysm 67 0.056
152
c HMP029 Hemophilia a 61 0.056
153
P THL005 Thalassemia 61 0.056
154
SRC014 Sarcoma 66 0.056
155
P ESN007 Eosinophilia 61 0.056
156
P PNM007 Pneumonia 67 0.056
157
P CRD011 Cardiomyopathy 66 0.056
158
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.056
159
BCT015 Bacteremia 50 0.056
160
P NRP001 Neuropathy 57 0.056
161
HYP063 Hypersplenism 49 0.056
162
MYT019 May-Thurner Syndrome 21 0.056
163
PRP080 Peripheral Artery Disease 35 0.056
164
c PRM225 Primary Thrombocytopenia 42 0.056
165
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.053
166
c ART101 Aortic Valve Disease 2 56 0.053
167
MYL009 Myelodysplastic Syndrome 73 0.053
168
P ART022 Arthritis 73 0.053
169
P HRD011 Hereditary Spherocytosis 51 0.053
170
P ASP006 Aspergillosis 61 0.053
171
P HYP076 Hyperthyroidism 59 0.053
172
P ESP024 Esophagitis 62 0.053
173
TTH006 Tooth Disease 52 0.053
174
ART017 Aortic Disease 57 0.053
175
BLR001 Biliary Atresia 52 0.053
176
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 36 0.053
177
PTR001 Petrositis 25 0.053
178
P END033 Endocarditis 52 0.053
179
c CHR431 Chronic Venous Insufficiency 43 0.053
180
P BRS047 Breast Cancer 100 0.049
181
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.049
182
P APL001 Aplastic Anemia 74 0.049
183
FCT007 Factor Vii Deficiency 60 0.049
184
P KDN018 Kidney Disease 64 0.049
185
ACR041 Acromelic Frontonasal Dysostosis 45 0.049
186
CHL071 Child Syndrome 58 0.049
187
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 41 0.049
188
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 59 0.049
189
ADL002 Adult Syndrome 53 0.049
190
c HPT001 Hepatitis C 68 0.049
191
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.049
192
c HPT016 Hepatitis B 61 0.049
193
INT007 Intermediate Coronary Syndrome 52 0.049
194
HRT007 Heart Cancer 51 0.049
195
KDS001 Kid Syndrome 53 0.049
196
TYP007 Typhoid Fever 61 0.049
197
CHL069 Cholesteatoma 51 0.049
198
c THR023 Thrombophilia Due to Thrombomodulin Defect 19 0.049
199
PRP016 Paraplegia 49 0.049
200
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 35 0.049
201
c ACT073 Acute Leukemia 61 0.049
202
P ABD003 Abdominal Aortic Aneurysm 43 0.049
203
OST017 Osteomyelitis 60 0.049
204
HRD083 Hereditary Antithrombin Deficiency 23 0.049
205
P AFB001 Afibrinogenemia 38 0.049
206
BRT030 Birth Defects 44 0.049
207
P HRT017 Heart Tumor 34 0.049
208
MDS022 Mediastinitis 37 0.049
209
HPT081 Hepatic Infarction 20 0.049
210
CRN030 Coronary Stenosis 50 0.049
211
c FRN011 Frontal Sinusitis 29 0.049
212
P RTN022 Retinal Vein Occlusion 36 0.049
213
CLP006 Clopidogrel Resistance 39 0.049
214
c ADL079 Adult Heart Tumor 17 0.049
215
PLM027 Pulmonary Embolism and Infarction 25 0.049
216
BRN106 Burns 52 0.049
217
THR035 Thrombasthenia 41 0.049
218
SCK003 Sickle Cell Anemia 72 0.046
219
c INF069 Infantile Neuroaxonal Dystrophy 1 44 0.046
220
P LPR003 Leprosy 70 0.046
221
RBR001 Roberts Syndrome 61 0.046
222
TTR001 Tetralogy of Fallot 69 0.046
223
THR104 Thrombophilia Due to Antithrombin Iii Deficiency 50 0.046
224
CRD119 Cardiac Arrest 63 0.046
225
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.046
226
MTH009 Mouth Disease 63 0.046
227
SCH014 Schistosomiasis 59 0.046
228
SPL012 Splenic Disease 48 0.046
229
P MMB011 Membranous Nephropathy 53 0.046
230
ALP043 Alpha-2-Plasmin Inhibitor Deficiency 35 0.046
231
THR088 Thrombophilia Due to Protein S Deficiency, Autosomal Recessive 18 0.046
232
SPH001 Sapho Syndrome 48 0.046
233
NWC001 Newcastle Disease 51 0.046
234
ZYG002 Zygomycosis 33 0.046
235
EXS001 Exostosis 42 0.046
236
DDN006 Duodenitis 44 0.046
237
c CRN177 Coronary Heart Disease 7 21 0.046
238
RTR011 Retroperitoneal Fibrosis 40 0.046
239
ERY004 Erysipelas 39 0.046
240
OCL006 Ocular Hypertension 47 0.046
241
P MYL007 Myeloma 52 0.046
242
CRD001 Cardiac Tamponade 43 0.046
243
ORL011 Oral Cancer 53 0.046
244
CTS005 Catastrophic Antiphospholipid Syndrome 39 0.046
245
P ACT061 Acute Sphenoidal Sinusitis 15 0.046
246
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 21 0.046
247
P PYL005 Pyelonephritis 52 0.046
248
HST009 Histiocytoma 47 0.046
249
ABD004 Abdominal Tuberculosis 37 0.046
250
SPN186 Spinal Cord Injury 62 0.046
251
c CRN173 Coronary Heart Disease 8 19 0.046
252
c CRN176 Coronary Heart Disease 9 19 0.046
253
GLC008 Glucose Metabolism Disease 44 0.046
254
STR044 Steroid-Resistant Nephrotic Syndrome 34 0.046
255
THN005 Thunderclap Headache 16 0.046
256
CGL001 Coagulation Protein Disease 14 0.046
257
CRB086 Cerebral Aneurysms 39 0.046
258
EYC003 Eye Accommodation Disease 25 0.046
259
BNF002 Bone Fracture 46 0.046
260
P LNG032 Lung Cancer 92 0.042
261
c HYP595 Hypertension, Essential 69 0.042
262
c MLT019 Multiple Myeloma 77 0.042
263
P PHC003 Pheochromocytoma 72 0.042
264
PCK002 Pick Disease 66 0.042
265
GST050 Gastrointestinal System Disease 58 0.042
266
P TRN020 Turner Syndrome 64 0.042
267
P TMP003 Temporal Arteritis 61 0.042
268
P SHR029 Short Syndrome 60 0.042
269
c HMP004 Hemophilia B 61 0.042
270
c THR082 Thrombophilia Due to Activated Protein C Resistance 57 0.042
271
VNW007 Von Willebrand Disease 57 0.042
272
BHC003 Behcet Syndrome 60 0.042
273
MDY003 Mody, Type Ii 36 0.042
274
HYP066 Hyperglycemia 61 0.042
275
ACT055 Actinomycosis 42 0.042
276
P INT070 Intestinal Obstruction 55 0.042
277
c CLD010 Cold-Induced Sweating Syndrome 1 43 0.042
278
SPT004 Septic Arthritis 60 0.042
279
APP008 Appendicitis 61 0.042
280
LCK001 Locked-in Syndrome 37 0.042
281
HMT002 Hematologic Cancer 62 0.042
282
DBT001 Diabetic Ketoacidosis 45 0.042
283
KLN001 Klinefelter's Syndrome 52 0.042
284
BLD034 Bile Duct Carcinoma 56 0.042
285
PRP007 Priapism 48 0.042
286
c THR048 Thrombocytopenia 4 29 0.042
287
P CRN035 Cranial Nerve Palsy 44 0.042
288
CDQ001 Cauda Equina Syndrome 40 0.042
289
WRF003 Warfarin Syndrome 30 0.042
290
MRB003 Morbid Obesity 59 0.042
291
ANR004 Anuria 46 0.042
292
HPT046 Hepatic Veno-Occlusive Disease 46 0.042
293
INT079 Intrahepatic Cholangiocarcinoma 55 0.042
294
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.042
295
ADN018 Adenoma 59 0.042
296
LNG095 Lung Abscess 34 0.042
297
SCR015 Scarlet Fever 37 0.042
298
CRH005 Crohn's Colitis 50 0.042
299
PLV003 Pelvic Inflammatory Disease 52 0.042
300
SPL018 Splenomegaly 45 0.042
301
CRT012 Cortical Blindness 36 0.042
302
CHL004 Cholelithiasis 48 0.042
303
PRS047 Prostatitis 56 0.042
304
FSC004 Fasciitis 47 0.042
305
PRT019 Protein-Losing Enteropathy 42 0.042
306
P CHL066 Cholangitis 48 0.042
307
c CNT016 Central Retinal Vein Occlusion 34 0.042
308
GST071 Gastrointestinal Carcinoma 37 0.042
309
SBD001 Subdural Empyema 30 0.042
310
BLD054 Blood Protein Disease 38 0.042
311
MCR225 Macrophage Activation Syndrome 39 0.042
312
BRN080 Brain Ischemia 42 0.042
313
ORB016 Orbital Varix 12 0.042
314
P RTN014 Retinal Artery Occlusion 32 0.042
315
CRB004 Cerebral Artery Occlusion 39 0.042
316
SNG003 Single Ventricular Heart 23 0.042
317
c CHR036 Chronic Cholangitis 25 0.042
318
HGH021 Hughes-Stovin Syndrome 18 0.042
319
ISC002 Ischemic Optic Neuropathy 45 0.042
320
THL018 Thalassemia Major 31 0.042
321
HMC014 Homocysteinemia 32 0.042
322
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.037
323
WST001 West Syndrome 61 0.037
324
WLL001 Williams-Beuren Syndrome 61 0.037
325
GST092 Gastroesophageal Reflux 62 0.037
326
MLN008 Melanoma 61 0.037
327
GLN010 Glanzmann Thrombasthenia 64 0.037
328
P PLR004 Pleuropulmonary Blastoma 63 0.037
329
PRT093 Proteus Syndrome, Somatic 54 0.037
330
VHW001 Vohwinkel Syndrome 47 0.037
331
DWN001 Down Syndrome 65 0.037
332
FCT006 Factor V Deficiency 62 0.037
333
P MYM002 Moyamoya Disease 60 0.037
334
P PSR002 Psoriasis 63 0.037
335
THR068 Thrombophilia Due to Protein C Deficiency, Autosomal Recessive 30 0.037
336
PHR003 Pharyngitis 58 0.037
337
P CNJ013 Conjunctivitis 65 0.037
338
PRP019 Peripheral Nervous System Disease 52 0.037
339
BRC012 Brucellosis 66 0.037
340
c THR037 Thrombocytopenia 2 36 0.037
341
P HML002 Hemolytic Anemia 60 0.037
342
CHL127 Cholangiocarcinoma, Susceptibility to 55 0.037
343
c HPT073 Hepatitis C Virus 72 0.037
344
MYH001 May-Hegglin Anomaly 41 0.037
345
EXF001 Exfoliation Syndrome 56 0.037
346
HYP080 Hypogonadism 54 0.037
347
LPD008 Lipid Metabolism Disorder 42 0.037
348
P EXP004 Exophthalmos 56 0.037
349
P ORL007 Oral Cavity Cancer 58 0.037
350
RHB003 Rhabdomyosarcoma 55 0.037
351
HMP005 Hemiplegia 52 0.037
352
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 0.037
353
HMR001 Hemorrhagic Thrombocythemia 47 0.037
354
ACQ007 Acquired Immunodeficiency Syndrome 60 0.037
355
TRC023 Trichinosis 44 0.037
356
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 42 0.037
357
LYM021 Lymphadenitis 58 0.037
358
ACT058 Active Peptic Ulcer Disease 44 0.037
359
P ENC004 Encephalitis 60 0.037
360
P PRX010 Paroxysmal Ventricular Fibrillation 33 0.037
361
CRN036 Craniopharyngioma 54 0.037
362
P BCL006 B-Cell Lymphomas 64 0.037
363
LPD004 Lipoid Nephrosis 49 0.037
364
P SLP006 Sleep Apnea 60 0.037
365
RLP001 Relapsing Polychondritis 52 0.037
366
THR089 Thrombophilia Due to Protein S Deficiency, Autosomal Dominant 21 0.037
367
VRC001 Varicocele 50 0.037
368
P LBY004 Labyrinthitis 39 0.037
369
THR067 Thrombophilia Due to Protein C Deficiency, Autosomal Dominant 22 0.037
370
P PLN008 Peeling Skin Syndrome 45 0.037
371
LYM040 Lymphoblastic Lymphoma 51 0.037
372
P PRT096 Peritoneal Mesothelioma 49 0.037
373
PRC013 Pericarditis 52 0.037
374
RDC002 Radiculopathy 53 0.037
375
RSD004 Rosai-Dorfman Disease 40 0.037
376
P THY032 Thyroiditis 57 0.037
377
P CMP008 Compartment Syndrome 46 0.037
378
VNF001 Vein of Galen Aneurysm 25 0.037
379
TNP003 Tn Polyagglutination Syndrome, Somatic 30 0.037
380
c BCT007 Bacterial Meningitis 55 0.037
381
P PNC001 Pancytopenia 53 0.037
382
HLL004 Hellp Syndrome 48 0.037
383
NDL013 Nodular Regenerative Hyperplasia 46 0.037
384
c INF067 Inflammatory Bowel Disease 10 31 0.037
385
INT253 Intestinal Benign Neoplasm 48 0.037
386
CHR001 Churg-Strauss Syndrome 48 0.037
387
OPT009 Optic Neuritis 48 0.037
388
c ACT134 Acute Liver Failure 46 0.037
389
URM002 Uremia 36 0.037
390
P LMY004 Leiomyosarcoma 54 0.037
391
MCN001 Mucinous Adenocarcinoma 48 0.037
392
GST053 Gastric Cancer 52 0.037
393
PRN021 Paranasal Sinus Disease 50 0.037
394
NRT004 Neuritis 52 0.037
395
SDD007 Sudden Cardiac Death 46 0.037
396
MYL001 Myelitis 35 0.037
397
EPD005 Epidural Abscess 32 0.037
398
CCN002 Cocaine Abuse 47 0.037
399
INT010 Intracranial Embolism 32 0.037
400
NSL022 Nasal Cavity Disease 41 0.037
401
MSN002 Mesenteric Lymphadenitis 40 0.037
402
INT221 Intravascular Large B-Cell Lymphoma 37 0.037
403
c CRN172 Coronary Heart Disease 3 19 0.037
404
SPN185 Spinal Cord Infarction 36 0.037
405
c ACT042 Acute Pyelonephritis 47 0.037
406
NNT044 Neonatal Antiphospholipid Syndrome 14 0.037
407
BCK006 Back Pain 40 0.037
408
CRB031 Cerebral Arterial Disease 31 0.037
409
NRN002 Neuronitis 40 0.037
410
IMP003 Impaired Renal Function Disease 36 0.037
411
WSC001 Wisconsin Syndrome 16 0.037
412
BRS090 Breast Reconstruction 38 0.037
413
ABD009 Abducens Palsy 17 0.037
414
LMB062 Limb Ischemia 48 0.037
415
P PNC035 Pancreatic Cancer 86 0.032
416
P STM004 Stomach Cancer 73 0.032
417
P CLR023 Colorectal Cancer 96 0.032
418
P MDL005 Medulloblastoma 76 0.032
419
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 61 0.032
420
OBS002 Obsessive-Compulsive Disorder 66 0.032
421
P CLC005 Celiac Disease 67 0.032
422
c PNC108 Pancreatitis, Hereditary 59 0.032
423
FML011 Familial Adenomatous Polyposis 68 0.032
424
CNG034 Congestive Heart Failure 72 0.032
425
P TBR001 Tuberous Sclerosis 68 0.032
426
VSC044 Visceral Myopathy 44 0.032
427
P DYS007 Dyskeratosis Congenita 64 0.032
428
P FCL005 Focal Segmental Glomerulosclerosis 59 0.032
429
DBN001 Dubin-Johnson Syndrome 52 0.032
430
P URF003 Urofacial Syndrome 1 51 0.032
431
c FML001 Familial Atrial Fibrillation 59 0.032
432
CMR002 Coumarin Resistance 49 0.032
433
LPT001 Leptospirosis 65 0.032
434
CCC001 Coccidioidomycosis 55 0.032
435
MLD001 Melioidosis 67 0.032
436
PLV005 Pelviureteric Junction Obstruction 43 0.032
437
TYP011 Typhus 57 0.032
438
P ERY048 Erythrocytosis, Familial, 2 42 0.032
439
CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 42 0.032
440
P MYP004 Myopathy 67 0.032
441
c PLN018 Peeling Skin Syndrome 2 36 0.032
442
P ANR007 Anorexia Nervosa 63 0.032
443
P ART023 Arthropathy 63 0.032
444
c ATM010 Autoimmune Hemolytic Anemia 59 0.032
445
P HYP086 Hypothyroidism 63 0.032
446
BRG013 Buerger Disease 54 0.032
447
CPL011 Capillary Malformations, Congenital, 1, Somatic, Mosaic 36 0.032
448
BNM001 Bone Marrow Cancer 56 0.032
449
P GRV001 Graves' Disease 62 0.032
450
ESP023 Esophageal Disease 52 0.032
451
P RBL001 Rubella 54 0.032
452
HYD012 Hydrops Fetalis 45 0.032
453
FCL012 Facial Paralysis 50 0.032
454
c HPT015 Hepatitis D 51 0.032
455
GNG013 Gingivitis 61 0.032
456
CHC001 Chickenpox 50 0.032
457
P END044 Endometriosis 53 0.032
458
SCR008 Scrub Typhus 55 0.032
459
P MST009 Mastocytosis 54 0.032
460
MNT001 Mantle Cell Lymphoma 72 0.032
461
P MTR012 Mitral Valve Disease 59 0.032
462
PNC034 Pancreas Disease 56 0.032
463
ESP002 Esophageal Varix 43 0.032
464
P ANP001 Anaplastic Large Cell Lymphoma 58 0.032
465
EBS001 Ebstein Anomaly 44 0.032
466
P ENC008 Encephalocele 48 0.032
467
P ECL001 Eclampsia 55 0.032
468
c HPT003 Hepatitis a 55 0.032
469
CLL002 Collecting Duct Carcinoma 43 0.032
470
P LYM025 Lymphedema 60 0.032
471
HNC001 Henoch-Schoenlein Purpura 45 0.032
472
SBS006 Sebastian Syndrome 36 0.032
473
LYM019 Lymphosarcoma 52 0.032
474
LGN002 Legionellosis 61 0.032
475
c PRC016 Pre-Eclampsia 57 0.032
476
c SYS004 Systemic Mastocytosis 60 0.032
477
TRN015 Transient Cerebral Ischemia 57 0.032
478
ECH003 Echinococcosis 53 0.032
479
c THR102 Thrombocytopenia 5 29 0.032
480
STM006 Stomach Disease 48 0.032
481
ADM013 Adamantinoma of Long Bones 57 0.032
482
WLL006 Wells Syndrome 57 0.032
483
TTL010 Total Anomalous Pulmonary Venous Return 34 0.032
484
ERD001 Erdheim-Chester Disease 51 0.032
485
P INT068 Intestinal Disease 60 0.032
486
PYD001 Pyoderma Gangrenosum 48 0.032
487
TNS005 Tonsillitis 58 0.032
488
P CTR002 Cataract 57 0.032
489
PLM001 Pulmonary Tuberculosis 69 0.032
490
CRT016 Carotid Artery Disease 54 0.032
491
DDN010 Duodenum Cancer 41 0.032
492
c CHR092 Chronic Myeloproliferative Disease 50 0.032
493
LRN003 Learning Disability 49 0.032
494
P PRD008 Periodontitis 46 0.032
495
P APL006 Aplasia Cutis Congenita 48 0.032
496
EVN001 Evans' Syndrome 39 0.032
497
TRN012 Transient Global Amnesia 38 0.032
498
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 35 0.032
499
END031 Endometrial Stromal Sarcoma 49 0.032
500
ALV002 Alveolar Echinococcosis 50 0.032
501
P NNT009 Neonatal Diabetes Mellitus 50 0.032
502
MYS004 Myiasis 31 0.032
503
STS002 Situs Inversus 43 0.032
504
PLS011 Plasmacytoma 57 0.032
505
END021 Endomyocardial Fibrosis 47 0.032
506
HPT008 Hepatic Tuberculosis 42 0.032
507
ACT017 Acute Chest Syndrome 50 0.032
508
CHR074 Choriocarcinoma 45 0.032
509
BRN014 Bronchopneumonia 45 0.032
510
NCR007 Necrotizing Fasciitis 43 0.032
511
BRN004 Brain Edema 51 0.032
512
PYD002 Pyoderma 46 0.032
513
VGN023 Vaginitis 41 0.032
514
P END047 Endophthalmitis 46 0.032
515
ILT001 Ileitis 48 0.032
516
MCR088 Microscopic Polyangiitis 47 0.032
517
GDS001 Good Syndrome 46 0.032
518
P RNV001 Renovascular Hypertension 46 0.032
519
OBS001 Obstructive Jaundice 47 0.032
520
INF034 Infective Endocarditis 50 0.032
521
PRC050 Pericardium Disease 32 0.032
522
WND002 Wandering Spleen 23 0.032
523
CYS009 Cystadenoma 40 0.032
524
c SBC003 Subacute Bacterial Endocarditis 33 0.032
525
VTM002 Vitamin B12 Deficiency 45 0.032
526
P CRV031 Cervical Adenocarcinoma 52 0.032
527
DDN007 Duodenal Disease 34 0.032
528
P PRP034 Purpura Fulminans 41 0.032
529
SPN035 Spindle Cell Sarcoma 48 0.032
530
PRN017 Perianal Hematoma 12 0.032
531
BRN026 Branch Retinal Artery Occlusion 37 0.032
532
GND003 Gonadal Disease 41 0.032
533
PHY002 Physical Disorder 43 0.032
534
HYP266 Hypoxia 55 0.032
535
SGN002 Signet Ring Cell Adenocarcinoma 45 0.032
536
ACL001 Acalculous Cholecystitis 35 0.032
537
HRS011 Horseshoe Kidney 34 0.032
538
SPC003 Specific Developmental Disorder 39 0.032
539
ETH009 Ethmoid Sinusitis 32 0.032
540
PLM013 Pulmonary Immaturity 38 0.032
541
THR007 Thrombophlebitis Migrans 18 0.032
542
CLN015 Colon Adenocarcinoma 55 0.032
543
ANG018 Angiomyolipoma 46 0.032
544
c ANT041 Antiphospholipid Syndrome, Familial 12 0.032
545
P CHR084 Chromosomal Disease 37 0.032
546
CVR001 Cavernous Sinus Meningioma 21 0.032
547
c ACT035 Acute Frontal Sinusitis 20 0.032
548
SHW001 Shwartzman Phenomenon 38 0.032
549
SXD001 Sex Differentiation Disease 39 0.032
550
ART004 Aortic Atherosclerosis 46 0.032
551
HST016 Histiocytic Sarcoma 38 0.032
552
FRN014 Fournier Gangrene 33 0.032
553
ESN011 Eisenmenger Syndrome 45 0.032
554
HNS001 Hansen's Disease 30 0.032
555
SYN036 Syncope 45 0.032
556
ALC005 Alcoholic Pancreatitis 35 0.032
557
c INH004 Inherited Blood Coagulation Disease 38 0.032
558
PRM008 Parametritis 28 0.032
559
INF013 Inferior Myocardial Infarction 36 0.032
560
HPT067 Hepatocellular Adenoma 41 0.032
561
PNM013 Pneumococcal Meningitis 41 0.032
562
P MXL015 Maxillary Sinusitis 36 0.032
563
DNT046 Dental Abscess 26 0.032
564
GLM011 Glomerulosclerosis 41 0.032
565
PRN039 Paraneoplastic Syndromes 42 0.032
566
CRT056 Carotidynia 13 0.032
567
P ACT080 Acute Pulmonary Heart Disease 31 0.032
568
c RNL016 Renal Infectious Disease 22 0.032
569
ART031 Aortic Coarctation 42 0.032
570
BSL004 Basilar Artery Occlusion 31 0.032
571
MND006 Mondor Disease 20 0.032
572
WTH001 Withdrawal Disorder 36 0.032
573
P GNT005 Giant Hemangioma 34 0.032
574
c ACT036 Acute Cholangitis 31 0.032
575
DBL009 Double Inferior Vena Cava 16 0.032
576
ACT174 Acute Peripheral Arterial Occlusion 16 0.032
577
BRN071 Brain Injury 51 0.032
578
HRD147 Hereditary Thrombophilia Due to Congenital Protein S Deficiency 11 0.032
579
OCL024 Ocular Neuromyotonia 12 0.032
580
CYS001 Cystic Fibrosis 87 0.026
581
P RHM011 Rheumatoid Arthritis 87 0.026
582
P OVR042 Ovarian Cancer 73 0.026
583
SKN016 Skin Disease 69 0.026
584
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 57 0.026
585
c CHR090 Chronic Lymphocytic Leukemia 73 0.026
586
ARG002 Argininosuccinic Aciduria 57 0.026
587
P KDN017 Kidney Cancer 67 0.026
588
MGR028 Migraine with or Without Aura 1 49 0.026
589
GST063 Gastric Cancer Risk After H. Pylori Infection 52 0.026
590
MVD001 Moved to 60 0.026
591
P ALX003 Alexander Disease 64 0.026
592
BRK010 Burkitt Lymphoma 66 0.026
593
P NRF002 Neurofibromatosis 66 0.026
594
MLG056 Malignant Hyperthermia 60 0.026
595
CRB037 Cerebral Palsy 54 0.026
596
ERY045 Erythrocytosis, Somatic 36 0.026
597
RSP006 Respiratory System Disease 61 0.026
598
P TRC086 Trichohepatoenteric Syndrome 1 46 0.026
599
P NRV007 Nervous System Disease 71 0.026
600
GLL032 Galloway-Mowat Syndrome 52 0.026
601
c AMY087 Amyloidosis, Hereditary, Transthyretin-Related 46 0.026
602
DNY001 Denys-Drash Syndrome 53 0.026
603
PTT046 Pituitary Hormone Deficiency, Combined, 2 54 0.026
604
MGL023 Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome, Somatic 34 0.026
605
OCL069 Ocular Motor Apraxia 44 0.026
606
LNG024 Langerhans-Cell Histiocytosis 64 0.026
607
MST016 Mesothelioma, Somatic 52 0.026
608
DRM006 Dermatitis 58 0.026
609
FCT003 Factor X Deficiency 62 0.026
610
P EHL001 Ehlers-Danlos Syndrome 61 0.026
611
SND002 Sneddon Syndrome 45 0.026
612
c ART115 Aortic Valve Disease 1 53 0.026
613
BRK001 Brooke-Spiegler Syndrome 47 0.026
614
c NRF018 Neurofibromatosis, Type 1 69 0.026
615
KLP010 Klippel-Trenaunay-Weber Syndrome 53 0.026
616
BLD087 Bladder Cancer, Somatic 54 0.026
617
c CHR089 Chronic Kidney Failure 67 0.026
618
RNL024 Renal Glucosuria 51 0.026
619
HND003 Hand-Foot-Uterus Syndrome 46 0.026
620
GNT031 Genitopatellar Syndrome 41 0.026
621
P HYP117 Hypertriglyceridemia 65 0.026
622
c KNB004 Knobloch Syndrome, Type 1 31 0.026
623
DRM014 Dermatofibrosarcoma Protuberans 61 0.026
624
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 45 0.026
625
PRC002 Paracoccidioidomycosis 57 0.026
626
VNW004 Von Willebrand Disease, Platelet-Type 40 0.026
627
ALL026 Allergic Hypersensitivity Disease 53 0.026
628
ATP002 Atopy 62 0.026
629
P MSC005 Muscular Dystrophy 64 0.026
630
SLP005 Sleep Disorder 52 0.026
631
P AST007 Astrocytoma 66 0.026
632
P SML016 Small Intestine Cancer 54 0.026
633
IRK001 Irak4 Deficiency 46 0.026
634
ERY029 Erythermalgia, Primary 40 0.026
635
c GRV008 Graves Disease 1 44 0.026
636
GLL018 Gallbladder Cancer 63 0.026
637
MCN017 Meconium Ileus 53 0.026
638
FRS002 Frasier Syndrome 48 0.026
639
QBC001 Quebec Platelet Disorder 51 0.026
640
c DYS165 Dysfibrinogenemia, Congenital 35 0.026
641
QFV001 Q Fever 62 0.026
642
c MLG054 Malignant Histiocytosis 55 0.026
643
P LNG064 Lung Cancer Susceptibility 3 62 0.026
644
HYP056 Hypoglycemia 60 0.026
645
BHR001 Behr Syndrome 43 0.026
646
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 32 0.026
647
P HMN010 Hemangioma 62 0.026
648
HMC038 Hemochromatosis, Neonatal 27 0.026
649
PGT003 Paget Disease, Extramammary 34 0.026
650
BLR007 Biliary Tract Neoplasm 49 0.026
651
CTS003 Coats Disease 57 0.026
652
P HRN001 Horner's Syndrome 45 0.026
653
TRP008 Tropical Calcific Pancreatitis 42 0.026
654
HPT074 Hepatic Adenoma, Somatic 35 0.026
655
CHP002 Chops Syndrome 36 0.026
656
ESN020 Eosinophilic Granulomatosis with Polyangiitis 38 0.026
657
HYP074 Hypersensitivity Vasculitis 49 0.026
658
UTR039 Uterine Fibroid 55 0.026
659
P HMR005 Hemorrhoid 45 0.026
660
ABD002 Abducens Nerve Disease 22 0.026
661
PLR007 Pleural Empyema 45 0.026
662
PSD007 Pseudomyxoma Peritonei 51 0.026
663
CNV002 Conversion Disorder 45 0.026
664
MVM001 Movement Disease 45 0.026
665
SVN001 Sveinsson Choreoretinal Atrophy 28 0.026
666
P TXP001 Toxoplasmosis 61 0.026
667
ALN001 Aland Island Eye Disease 45 0.026
668
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 30 0.026
669
PMP001 Pemphigus 49 0.026
670
GLY032 Glycosylphosphatidylinositol Deficiency 24 0.026
671
GST060 Gastric Cancer, Somatic 44 0.026
672
TXC005 Toxic Shock Syndrome 61 0.026
673
c MYH004 Myh9 Related Thrombocytopenia 21 0.026
674
RPR002 Reproductive System Disease 45 0.026
675
P HST010 Histiocytosis 56 0.026
676
ORB013 Orbital Disease 41 0.026
677
LGN004 Legionaire Disease 33 0.026
678
CYS008 Cystic Echinococcosis 48 0.026
679
MYD002 Myd88 Deficiency 47 0.026
680
CHL123 Chlamydia 60 0.026
681
c TRC078 Trichohepatoenteric Syndrome 2 30 0.026
682
PRX023 Paroxysmal Nocturnal Hemoglobinuria, Somatic 20 0.026
683
HMR004 Hemorrhagic Fever with Renal Syndrome 52 0.026
684
BLR027 Blue Rubber Bleb Nevus 33 0.026
685
TRN004 Trench Fever 38 0.026
686
P PRM006 Primary Biliary Cirrhosis 55 0.026
687
GSG001 Gas Gangrene 49 0.026
688
CRY004 Cryoglobulinemia 47 0.026
689
ADL030 Adult-Onset Still's Disease 57 0.026
690
c PLN021 Peeling Skin Syndrome 3 30 0.026
691
THR020 Thrombophilia Due to Heparin Cofactor Ii Deficiency 21 0.026
692
P DBT005 Diabetes Insipidus 53 0.026
693
OBS061 Obstructive Sleep Apnea 61 0.026
694
P OVR049 Ovarian Disease 54 0.026
695
DFF021 Diffuse Mesangial Sclerosis 40 0.026
696
INT051 Intussusception 50 0.026
697
c VRL010 Viral Hepatitis 60 0.026
698
P SYR001 Syringomyelia 44 0.026
699
PLM010 Pulmonary Edema 56 0.026
700
AYM001 Ayme-Gripp Syndrome 40 0.026
701
c PLN017 Peeling Skin Syndrome 1 32 0.026
702
ALP072 Alpha-Fetoprotein Deficiency 25 0.026
703
P PLY014 Polycystic Kidney Disease 60 0.026
704
c BRN108 Branchiootic Syndrome 1 36 0.026
705
PMS001 Poems Syndrome 56 0.026
706
P GND004 Gonadal Dysgenesis 51 0.026
707
c ANR038 Anorexia Nervosa 1 28 0.026
708
P OVR046 Ovarian Cyst 48 0.026
709
END030 End Stage Renal Failure 53 0.026
710
PNC033 Pancreas Adenocarcinoma 54 0.026
711
P THR003 Thoracic Aortic Aneurysm 57 0.026
712
ALX001 Alexia 42 0.026
713
CNN005 Connective Tissue Disease 60 0.026
714
c HMG003 Hemoglobin E Disease 44 0.026
715
P FML035 Familial Hyperlipidemia 49 0.026
716
PRN011 Pernicious Anemia 41 0.026
717
MGC001 Megacolon 50 0.026
718
PNC013 Pancreatic Ductal Carcinoma 45 0.026
719
PRN019 Perinatal Necrotizing Enterocolitis 47 0.026
720
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 21 0.026
721
APP009 Appendix Adenocarcinoma 40 0.026
722
PRT012 Prothrombin Deficiency 43 0.026
723
SPR007 Superior Mesenteric Artery Syndrome 37 0.026
724
APP010 Appendix Cancer 38 0.026
725
BCT002 Bacterial Vaginosis 53 0.026
726
FML039 Female Reproductive System Disease 49 0.026
727
THR021 Thrombophilia Due to Hrg Deficiency 18 0.026
728
GBL002 Goblet Cell Carcinoid 29 0.026
729
c PSR019 Psoriasis Susceptibility 13 24 0.026
730
P HYP060 Hyperinsulinism 58 0.026
731
P SHR001 Short Bowel Syndrome 51 0.026
732
c ACT071 Acute Kidney Failure 48 0.026
733
FBR028 Fibrosing Mediastinitis 24 0.026
734
EYL001 Eyelid Neoplasm 33 0.026
735
P MYC008 Myocarditis 56 0.026
736
BCT004 Bacteriuria 48 0.026
737
RTC001 Reticulohistiocytic Granuloma 32 0.026
738
AMP003 Ampulla of Vater Neoplasm 35 0.026
739
PSR005 Psoriasis, Protection Against 18 0.026
740
c MLG069 Malignant Hypertension 46 0.026
741
SYR002 Syringocystadenoma Papilliferum 43 0.026
742
DRS001 Dressler's Syndrome 34 0.026
743
INT038 Interdigitating Dendritic Cell Sarcoma 35 0.026
744
ANG066 Angel-Shaped Phalangoepiphyseal Dysplasia 21 0.026
745
BRW006 Brown Syndrome 31 0.026
746
c PRT045 Prothrombin-Related Thrombophilia 25 0.026
747
SXL003 Sexual Disorder 45 0.026
748
PRS045 Prostatic Hypertrophy 44 0.026
749
PRC012 Pericardial Effusion 50 0.026
750
DYS015 Dysentery 42 0.026
751
HYD002 Hydronephrosis 48 0.026
752
HYP458 Hyper Ige Syndrome 43 0.026
753
BRN015 Bronchiolo-Alveolar Adenocarcinoma 37 0.026
754
LNG004 Langerhans Cell Sarcoma 35 0.026
755
CHL070 Cholesterol Embolism 31 0.026
756
CTN004 Cutaneous Fibrous Histiocytoma 41 0.026
757
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 21 0.026
758
FCT008 Factitious Disorder 42 0.026
759
SML036 Small Intestinal Adenocarcinoma 46 0.026
760
HDG003 Hodgkin's Lymphoma, Lymphocytic Depletion 33 0.026
761
AMP009 Ampulla of Vater Adenocarcinoma 34 0.026
762
PPL018 Papillary Adenocarcinoma 48 0.026
763
NNT024 Neonatal Stroke 34 0.026
764
LYM014 Lymphangitis 35 0.026
765
KRN001 Korean Hemorrhagic Fever 39 0.026
766
AML001 Amelanotic Melanoma 40 0.026
767
LYM005 Lymphocele 37 0.026
768
INP001 Inappropriate Adh Syndrome 34 0.026
769
MXD023 Mixed Cell Type Cancer 45 0.026
770
YNG002 Young Syndrome 25 0.026
771
JNT002 Joint Disorders 55 0.026
772
CRD023 Cardiomyopathy Cataract Hip Spine Disease 15 0.026
773
CRV068 Cervical Polyp 40 0.026
774
GST040 Gastric Adenocarcinoma 57 0.026
775
c CHR047 Chronic Ethmoiditis 27 0.026
776
ALK015 Alk-Positive Anaplastic Large Cell Lymphoma 37 0.026
777
c ANT034 Anterior Uveitis 49 0.026
778
JPN001 Japanese Spotted Fever 31 0.026
779
LBL001 Lobular Neoplasia 48 0.026
780
PLR008 Pleurisy 51 0.026
781
MCN008 Mucinous Cystadenocarcinoma 39 0.026
782
MLK004 Malakoplakia 28 0.026
783
ASP003 Aseptic Meningitis 51 0.026
784
BLD005 Bile Duct Mucoepidermoid Carcinoma 31 0.026
785
BLD019 Bile Duct Cystadenocarcinoma 32 0.026
786
P CNG390 Congenital Pulmonary Airway Malformation 41 0.026
787
P PLY041 Polymyositis 49 0.026
788
VSC009 Vascular Skin Disease 21 0.026
789
DRM013 Dermoid Cyst 39 0.026
790
PRS115 Prosthetic Joint Infection 45 0.026
791
CRT013 Carotid Stenosis 35 0.026
792
NSL003 Nasal Cavity Adenocarcinoma 40 0.026
793
MNN005 Meningovascular Neurosyphilis 24 0.026
794
SPL004 Splenic Marginal Zone Lymphoma 43 0.026
795
PRP028 Peripheral Vertigo 42 0.026
796
ADN013 Adenoid Squamous Cell Carcinoma 35 0.026
797
CTN012 Cutaneous Leiomyosarcoma 38 0.026
798
MYS002 Myositis Fibrosa 35 0.026
799
LCH001 Leech Infestation 35 0.026
800
NRR001 Neuroretinitis 41 0.026
801
VLV008 Vulvitis 34 0.026
802
CNS002 Constrictive Pericarditis 31 0.026
803
ABR002 Abrikosov's Tumor 27 0.026
804
c CNT028 Central Retinal Artery Occlusion 34 0.026
805
PRL008 Paralytic Ileus 37 0.026
806
BLD045 Bladder Diverticulum 31 0.026
807
c ACQ014 Acquired Hemophilia 42 0.026
808
c ACT059 Acute Maxillary Sinusitis 38 0.026
809
CCM001 Cecum Adenocarcinoma 38 0.026
810
P LPS002 Liposarcoma 50 0.026
811
LYM006 Lymphoepithelioma-Like Carcinoma 42 0.026
812
PNC041 Pancreatic Ductal Adenocarcinoma 64 0.026
813
PRD003 Periodontosis 40 0.026
814
MCR011 Microinvasive Gastric Cancer 35 0.026
815
TBL003 Tubular Adenocarcinoma 41 0.026
816
WDS002 Woods Syndrome 30 0.026
817
P GNT008 Giant Cell Tumor 51 0.026
818
ANL014 Anal Canal Adenocarcinoma 30 0.026
819
OVR054 Ovarian Mucinous Neoplasm 35 0.026
820
PYL004 Pyelitis 39 0.026
821
NDL002 Nodular Tenosynovitis 23 0.026
822
SMN007 Seminoma 45 0.026
823
c MLG002 Malignant Peritoneal Mesothelioma 44 0.026
824
FLL029 Fallopian Tube Disease 33 0.026
825
BWN002 Bowen Syndrome 22 0.026
826
c RCR022 Recurrent Acute Pancreatitis 36 0.026
827
c FML015 Familial Nephrotic Syndrome 33 0.026
828
TMR001 Tumor of Exocrine Pancreas 28 0.026
829
CNN002 Cannabis Abuse 37 0.026
830
P ACT077 Acute Orbital Inflammation 15 0.026
831
GLB003 Globe Disease 34 0.026
832
GST017 Gastric Tubular Adenocarcinoma 30 0.026
833
ANT022 Anterior Cranial Fossa Meningioma 26 0.026
834
APP003 Appendiceal Neoplasm 37 0.026
835
END074 Endocardium Disease 26 0.026
836
BNT001 Banti's Syndrome 17 0.026
837
PLY010 Polyclonal Hypergammaglobulinemia 31 0.026
838
PNC002 Pancreatic Mucinous Cystadenoma 35 0.026
839
RCT020 Rectum Adenocarcinoma 30 0.026
840
P PRN022 Perineurioma 37 0.026
841
MCN005 Mucinous Intrahepatic Cholangiocarcinoma 20 0.026
842
MNN002 Mononeuritis Multiplex 26 0.026
843
MNN009 Meningoencephalitis 42 0.026
844
MRP002 Morpheaform Basal Cell Carcinoma 24 0.026
845
NNL001 Non-Langerhans-Cell Histiocytosis 38 0.026
846
P SLP003 Salpingitis 32 0.026
847
THY024 Thymus Adenocarcinoma 28 0.026
848
TNS001 Tenosynovial Giant Cell Tumor 31 0.026
849
UPP004 Upper Respiratory Tract Disease 48 0.026
850
DND018 Dendritic Cell Tumor 40 0.026
851
EPT011 Epithelioid Leiomyosarcoma 39 0.026
852
ADN027 Adenomyosis 45 0.026
853
ADN075 Adenomyoma 31 0.026
854
c CHR097 Chronic Purulent Otitis Media 22 0.026
855
c BLR016 Biliary Cirrhosis, Primary, 2 16 0.026
856
c BLR026 Biliary Cirrhosis, Primary, 5 14 0.026
857
LNT001 Linitis Plastica 32 0.026
858
PRP050 Peripheral Arterial Occlusive Disease 1 16 0.026
859
NVS004 Nova Syndrome 18 0.026
860
MCR014 Microcystic Adenoma 24 0.026
861
MRN001 Marantic Endocarditis 34 0.026
862
SKL006 Skull Base Neoplasm 24 0.026
863
SPN119 Spondylarthropathy 46 0.026
864
TRN007 Transsexualism 41 0.026
865
TXC001 Toxic Megacolon 26 0.026
866
OBS004 Obstructive Hydrocephalus 33 0.026
867
P CYS017 Cystic Teratoma 40 0.026
868
P DRM012 Dermis Tumor 28 0.026
869
EPS023 Epstein-Barr Virus-Associated Gastric Carcinoma 42 0.026
870
BLR005 Biliary Papillomatosis 34 0.026
871
BPH002 Biphasic Synovial Sarcoma 28 0.026
872
HST008 Histiocytic and Dendritic Cell Cancer 24 0.026
873
c HYP072 Hypersensitivity Reaction Type Iii Disease 39 0.026
874
MCN003 Mucinous Ovarian Cystadenoma 21 0.026
875
MDD010 Middle Ear Disease 47 0.026
876
MCN004 Mucinous Tubular and Spindle Renal Cell Carcinoma 26 0.026
877
CYS003 Cystitis Cystica 31 0.026
878
CNT046 Central Nervous System Vasculitis 44 0.026
879
c INF078 Inflammatory Bowel Disease 2 23 0.026
880
OCL025 Ocular Toxoplasmosis 40 0.026
881
SCR001 Secretory Meningioma 36 0.026
882
VLL006 Villous Adenoma 32 0.026
883
BLD032 Bile Duct Adenocarcinoma 39 0.026
884
CRV030 Cervical Adenitis 30 0.026
885
GLN006 Glandular Cystitis 23 0.026
886
BLT003 Blue Toe Syndrome 33 0.026
887
BRN021 Brain Sarcoma 30 0.026
888
OVR011 Ovarian Mucinous Adenocarcinoma 27 0.026
889
PLX004 Plexopathy 29 0.026
890
PRT031 Parotid Disease 28 0.026
891
P PNC043 Pancreatic Intraductal Papillary-Mucinous Neoplasm 37 0.026
892
MLG018 Malignant Giant Cell Tumor of Soft Parts 25 0.026
893
MSN003 Mesenteric Vascular Occlusion 34 0.026
894
SCT001 Sciatic Neuropathy 38 0.026
895
STR077 Streptococcal Toxic-Shock Syndrome 38 0.026
896
THY007 Thymus Lipoma 24 0.026
897
DDN009 Duodenal Obstruction 35 0.026
898
INT050 Intestinal Impaction 28 0.026
899
c FML269 Familial Idiopathic Steroid-Resistant Nephrotic Syndrome with Focal Segmental Hyalinosis 23 0.026
900
c GST048 Gastrointestinal System Benign Neoplasm 40 0.026
901
ALK005 Alk+ Histiocytosis 11 0.026
902
CLR109 Colorectal Adenocarcinoma 50 0.026
903
END075 Endocervical Adenocarcinoma 34 0.026
904
c ADN012 Adenocarcinoma in Situ 44 0.026
905
c CHR087 Chronic Cystitis 32 0.026
906
HMN016 Hemangioendothelioma 40 0.026
907
HPT079 Hepatoid Adenocarcinoma 29 0.026
908
JJN007 Jejunal Adenocarcinoma 29 0.026
909
PRR008 Periarteritis Nodosa 28 0.026
910
IMM006 Immune System Organ Benign Neoplasm 26 0.026
911
INF022 Inflamed Seborrheic Keratosis 12 0.026
912
SPP004 Suppurative Cholangitis 35 0.026
913
SRN001 Serine Deficiency 31 0.026
914
TRM010 Traumatic Brain Injury 52 0.026
915
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 14 0.026
916
GRN003 Granulomatous Dermatitis 32 0.026
917
c ACT066 Acute Cervicitis 31 0.026
918
CLL009 Colloid Carcinoma of the Pancreas 32 0.026
919
MNN014 Mononeuritis 24 0.026
920
URT010 Ureteral Obstruction 45 0.026
921
VGN010 Vaginal Tubulovillous Adenoma 13 0.026
922
VGN015 Vaginal Adenoma 17 0.026
923
P ATM020 Autoimmune Enteropathy 37 0.026
924
CRB087 Cerebral Arteriosclerosis 23 0.026
925
c FML230 Familial Idiopathic Steroid-Resistant Nephrotic Syndrome with Diffuse Mesangial Proliferation 10 0.026
926
c FML267 Familial Idiopathic Steroid-Resistant Nephrotic Syndrome with Diffuse Mesangial Sclerosis 16 0.026
927
c FML268 Familial Idiopathic Steroid-Resistant Nephrotic Syndrome with Minimal Changes 20 0.026
928
AGG003 Aggressive Digital Papillary Adenocarcinoma 35 0.026
929
PRM025 Primary Bacterial Infectious Disease 42 0.026
930
NRS005 Neurosarcoidosis 20 0.026
931
MTH044 Mthfr Gene Mutation 21 0.026
932
c SLC030 Slc6a4-Related Altered Drug Metabolism 11 0.026
933
P SPR075 Sporadic Idiopathic Steroid-Resistant Nephrotic Syndrome with Diffuse Mesangial Sclerosis 11 0.026
934
ATR024 Atrial Fibrillation and Stroke 19 0.026
935
c VGN016 Vaginal Benign Neoplasm 15 0.026
936
c PRS050 Prss1-Related Hereditary Pancreatitis 19 0.026
937
P PRS040 Prostate Cancer 89 0.019
938
c LKM061 Leukemia, Acute Myeloid 71 0.019
939
FBR012 Fabry Disease 68 0.019
940
P HNT016 Huntington Disease 80 0.019
941
P HYP607 Hypercholesterolemia, Familial 77 0.019
942
MLR004 Malaria 80 0.019
943
ESP021 Esophageal Cancer 75 0.019
944
P NRB001 Neuroblastoma 70 0.019
945
HDG012 Hodgkin Lymphoma 75 0.019
946
ADN021 Adenomatous Polyposis Coli 71 0.019
947
HV1006 Hiv-1 80 0.019
948
P OST005 Osteogenesis Imperfecta 68 0.019
949
LSC001 Lesch-Nyhan Syndrome 60 0.019
950
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 60 0.019
951
P HMC003 Hemochromatosis 71 0.019
952
CYS036 Cystinosis, Nephropathic 40 0.019
953
PTZ001 Peutz-Jeghers Syndrome 71 0.019
954
P PRM019 Premature Ovarian Failure 65 0.019
955
GLT021 Glutaricaciduria, Type I 47 0.019
956
ORN006 Ornithine Transcarbamylase Deficiency 60 0.019
957
CNT098 Central Core Disease 68 0.019
958
P CSH001 Cushing's Syndrome 65 0.019
959
DCH001 Duchenne Muscular Dystrophy 81 0.019
960
P ADD001 Addison's Disease 60 0.019
961
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.019
962
P WSK001 Wiskott-Aldrich Syndrome 70 0.019
963
ETH011 Ethylmalonic Encephalopathy 57 0.019
964
CRZ001 Crouzon Syndrome 70 0.019
965
c DLT002 Dilated Cardiomyopathy 75 0.019
966
P OST012 Osteoarthritis 81 0.019
967
ART002 Arts Syndrome 53 0.019
968
P SPN046 Spinal Muscular Atrophy 62 0.019
969
P SZR006 Seizure Disorder 56 0.019
970
c OST135 Osteogenesis Imperfecta, Type I 54 0.019
971
BCK001 Becker Muscular Dystrophy 68 0.019
972
FRB001 Farber Lipogranulomatosis 54 0.019
973
c FNC027 Fanconi Anemia, Complementation Group a 71 0.019
974
P ATP001 Atopic Dermatitis 60 0.019
975
STT001 Status Epilepticus 59 0.019
976
P STR020 Strabismus 55 0.019
977
P PRD006 Prader-Willi Syndrome 64 0.019
978
JCB001 Jacobsen Syndrome 49 0.019
979
P ERY008 Erythromelalgia 50 0.019
980
STR079 Sturge-Weber Syndrome, Somatic, Mosaic 39 0.019
981
PTT049 Pituitary Adenoma, Acth-Secreting 52 0.019
982
NTH001 Netherton Syndrome 52 0.019
983
P DMN001 Diamond-Blackfan Anemia 69 0.019
984
CYS010 Cystinosis 51 0.019
985
CHN016 Cohen Syndrome 55 0.019
986
P LYM007 Lymphangioleiomyomatosis 65 0.019
987
P CRP007 Carpenter Syndrome 49 0.019
988
P PRT010 Parathyroid Carcinoma 61 0.019
989
WGN006 Wegener Granulomatosis 63 0.019
990
ENC044 Enchondromatosis, Multiple, Ollier Type 44 0.019
991
ART001 Arterial Tortuosity Syndrome 51 0.019
992
c CNG189 Congenital Disorder of Glycosylation, Type Ib 34 0.019
993
CRT002 Cartilage-Hair Hypoplasia 57 0.019
994
CHY002 Chylomicron Retention Disease 54 0.019
995
P HYP061 Hypertrophic Cardiomyopathy 64 0.019
996
c PLM132 Pulmonary Venoocclusive Disease 2 32 0.019
997
TST021 Testicular Germ Cell Tumor 67 0.019
998
NTR005 Nutritional Deficiency Disease 51 0.019
999
c PRM012 Primary Polycythemia 48 0.019
1000
NRC019 Neurocutaneous Melanosis, Somatic 38 0.019
1001
P INF032 Infertility 61 0.019
1002
RCT018 Rectal Neoplasm 53 0.019
1003
c ACT210 Acute Respiratory Distress Syndrome 55 0.019
1004
P PTS002 Ptosis 56 0.019
1005
P PLY011 Polycystic Ovary Syndrome 64 0.019
1006
GST023 Gastric Ulcer 56 0.019
1007
P DRM010 Dermatomyositis 59 0.019
1008
P GST044 Gastritis 64 0.019
1009
c CNG379 Congenital Disorder of Glycosylation, Type It 28 0.019
1010
URN009 Urinary System Disease 52 0.019
1011
SVR004 Severe Combined Immunodeficiency 71 0.019
1012
c MTB001 Metabolic Syndrome X 61 0.019
1013
P VGN017 Vaginal Cancer 44 0.019
1014
HRP004 Herpes Zoster 56 0.019
1015
IMM096 Immunodeficiency 30 30 0.019
1016
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 55 0.019
1017
P HRM001 Hermansky-Pudlak Syndrome 56 0.019
1018
P ADM011 Adams-Oliver Syndrome 51 0.019
1019
c CHR579 Chiari Malformation Type Ii 38 0.019
1020
P MCR010 Microcephaly 60 0.019
1021
P CHN012 Chondrosarcoma 57 0.019
1022
P PLY006 Polydactyly 56 0.019
1023
CCT002 Cicatricial Pemphigoid 50 0.019
1024
VNW005 Von Willebrand Disease, Type 1 48 0.019
1025
CNG048 Congenital Hepatic Fibrosis 47 0.019
1026
MTN003 Motion Sickness 48 0.019
1027
P PLY017 Polyarteritis Nodosa 54 0.019
1028
P INF038 Influenza 71 0.019
1029
SCT005 Scott Syndrome 51 0.019
1030
BRN038 Bronchial Disease 54 0.019
1031
GTR002 Goiter 54 0.019
1032
P HRP006 Herpes Simplex 65 0.019
1033
P PLM025 Pulmonary Venoocclusive Disease 48 0.019
1034
P IGN003 Iga Nephropathy 1 31 0.019
1035
P GLB002 Glioblastoma 65 0.019
1036
EYD002 Eye Disease 62 0.019
1037
c MCR115 Microvascular Complications of Diabetes 5 60 0.019
1038
MLT145 Multiple Enchondromatosis, Maffucci Type 48 0.019
1039
END020 Endocardial Fibroelastosis 44 0.019
1040
c MCR129 Microvascular Complications of Diabetes 1 55 0.019
1041
P MGS004 Meige Syndrome 46 0.019
1042
CDS002 Codas Syndrome 38 0.019
1043
IMM102 Immunodeficiency 14 33 0.019
1044
P PRP029 Porphyria 56 0.019
1045
IMP002 Imperforate Anus 54 0.019
1046
c ATM003 Autoimmune Thyroiditis 59 0.019
1047
JPN002 Japanese Encephalitis 51 0.019
1048
BNC003 Bone Cancer 44 0.019
1049
P MYS005 Myositis 57 0.019
1050
CYS005 Cysticercosis 52 0.019
1051
P VNT002 Ventricular Septal Defect 59 0.019
1052
SPN041 Spinal Cord Disease 50 0.019
1053
CMP010 Complex Regional Pain Syndrome 59 0.019
1054
OLV001 Olivopontocerebellar Atrophy 53 0.019
1055
P INT143 Interstitial Cystitis 57 0.019
1056
PLN006 Poland Syndrome 48 0.019
1057
MDY006 Mody, Type Iv 31 0.019
1058
P CRB042 Cerebellar Ataxia 64 0.019