Search results for "thrombosis"

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

1387 hits were found for 'thrombosis'

# Family MCID Name MIFTS Score
1
c THR092 Thrombophilia Due to Thrombin Defect 56 5.901
2
SGT001 Sagittal Sinus Thrombosis 33 5.884
3
PRT018 Portal Vein Thrombosis 49 5.637
4
CRN017 Coronary Thrombosis 48 5.548
5
LTR002 Lateral Sinus Thrombosis 27 5.097
6
CVR002 Cavernous Sinus Thrombosis 28 4.817
7
CRT004 Carotid Artery Thrombosis 41 4.637
8
INT076 Intracranial Sinus Thrombosis 24 3.931
9
P BDD001 Budd-Chiari Syndrome 56 3.585
10
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 18 3.350
11
THR055 Thrombophilia, X-Linked, Due to Factor Ix Defect 17 2.742
12
CRB132 Cerebral Sinovenous Thrombosis 31 2.260
13
HMC020 Homocystinuria, B6-Responsive and Nonresponsive Types 55 1.961
14
FCT013 Factor V Leiden Thrombophilia 21 1.951
15
VNS012 Venous Thoracic Outlet Syndrome 15 1.939
16
CRB009 Cerebritis 38 0.460
17
PLM033 Pulmonary Embolism 59 0.278
18
VND001 Vein Disease 52 0.271
19
P MYC007 Myocardial Infarction 79 0.245
20
P THR015 Thrombophilia 59 0.236
21
P HPT021 Hepatitis 70 0.235
22
PRT014 Protein S Deficiency 52 0.232
23
VSC007 Vascular Disease 67 0.230
24
P THR014 Thrombocytopenia 64 0.223
25
HPR003 Heparin-Induced Thrombocytopenia 46 0.214
26
P ANT006 Antiphospholipid Syndrome 58 0.199
27
PRT011 Protein C Deficiency 51 0.197
28
HPT023 Hepatocellular Carcinoma 91 0.187
29
ANR040 Aneurysm 57 0.179
30
END072 Endotheliitis 42 0.162
31
P ESS003 Essential Thrombocythemia 68 0.157
32
c SYS001 Systemic Lupus Erythematosus 87 0.155
33
P LPS004 Lupus Erythematosus 63 0.153
34
HYP037 Hyperhomocysteinemia 50 0.153
35
c BLD124 Bleeding Disorder, Platelet-Type, 11 42 0.150
36
PST095 Post-Thrombotic Syndrome 50 0.147
37
LVR012 Liver Cirrhosis 67 0.142
38
c ACT075 Acute Myocardial Infarction 60 0.139
39
P LKM002 Leukemia 70 0.134
40
P PNC044 Pancreatitis 60 0.127
41
ART111 Artery Disease 57 0.127
42
P PLY018 Polycythemia 57 0.126
43
VSC006 Vascular Cancer 54 0.126
44
CRD118 Cardiovascular Cancer 47 0.124
45
CLT003 Colitis 59 0.121
46
PRP027 Peripheral Vascular Disease 69 0.118
47
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.118
48
THR016 Thrombophlebitis 52 0.118
49
HMG002 Hemoglobinuria 49 0.118
50
ATH003 Atherosclerosis 62 0.117
51
P PRT013 Portal Hypertension 59 0.117
52
ULC004 Ulcerative Colitis 75 0.115
53
HDC001 Headache 54 0.115
54
BLD053 Blood Platelet Disease 46 0.112
55
P CRN211 Coronary Artery Disease 75 0.111
56
ISC004 Ischemia 59 0.111
57
P BLD051 Blood Coagulation Disease 45 0.111
58
VSC008 Vascular Hemostatic Disease 33 0.111
59
P SNS014 Sinusitis 60 0.109
60
HPT020 Hepatic Vascular Disease 44 0.109
61
P MNN013 Meningitis 65 0.102
62
THR004 Thrombocytosis 55 0.102
63
RTN023 Retinitis 49 0.100
64
P HRT032 Heart Disease 76 0.099
65
P LVR013 Liver Disease 72 0.099
66
DSS009 Disseminated Intravascular Coagulation 51 0.099
67
MST019 Mastoiditis 33 0.099
68
P HYP098 Hypereosinophilic Syndrome 51 0.097
69
P ADN016 Adenocarcinoma 69 0.095
70
OTT002 Otitis Media 66 0.095
71
INT003 Intracranial Hypotension 39 0.095
72
P LYM118 Lymphoma 70 0.093
73
STR067 Stroke, Ischemic 77 0.091
74
PRP030 Purpura 59 0.091
75
CLL003 Cellulitis 49 0.091
76
P ART084 Arteriovenous Fistula 44 0.091
77
P VNS003 Venous Insufficiency 53 0.089
78
HDN002 Head Injury 45 0.089
79
OVR029 Ovarian Hyperstimulation Syndrome 60 0.087
80
INT075 Intracranial Hypertension 53 0.087
81
TBR010 Tuberculosis 69 0.085
82
ART021 Arteriosclerosis 59 0.083
83
SPN340 Spontaneous Intracranial Hypotension 23 0.083
84
ADJ001 Adjustment Disorder 38 0.080
85
c MYC058 Myocardial Infarction 2 29 0.080
86
c CRN175 Coronary Heart Disease 4 21 0.078
87
P OBS005 Obesity 93 0.076
88
CRN006 Coronary Aneurysm 32 0.076
89
P LYM026 Lymphoblastic Leukemia 60 0.073
90
P PLM037 Pulmonary Hypertension 79 0.071
91
c ACT027 Acute Pancreatitis 56 0.071
92
MYM001 Myoma 51 0.071
93
ANG054 Angina Pectoris 51 0.071
94
PPL021 Papilledema 48 0.071
95
CRD137 Cardiogenic Shock 46 0.071
96
P DYS026 Dysfibrinogenemia 41 0.071
97
P CRN178 Coronary Heart Disease 6 24 0.071
98
c CRN214 Coronary Heart Disease 5 23 0.071
99
CRH001 Crohn's Disease 76 0.068
100
ISC006 Ischemic Heart Disease 68 0.068
101
P MYL005 Myelofibrosis 67 0.068
102
CSY001 C Syndrome 49 0.068
103
SPL006 Splenic Infarction 35 0.068
104
SPR035 Superior Vena Cava Syndrome 32 0.068
105
ORB006 Orbital Cellulitis 28 0.068
106
DFC004 Deficiency Anemia 65 0.066
107
P ATR011 Atrial Fibrillation 64 0.066
108
VSC011 Vasculitis 62 0.066
109
P HMP007 Hemophilia 56 0.066
110
IRN001 Iron Deficiency Anemia 51 0.066
111
FCT004 Factor Xii Deficiency 51 0.066
112
P RNL014 Renal Cell Carcinoma 81 0.063
113
P MYL006 Myeloid Leukemia 67 0.063
114
P GLM007 Glomerulonephritis 56 0.063
115
PTN001 Patent Foramen Ovale 54 0.063
116
P SPS003 Spastic Diplegia 53 0.063
117
CYT008 Cytomegalovirus Infection 51 0.063
118
THR013 Thoracic Outlet Syndrome 49 0.063
119
P OST028 Osteochondroma 48 0.063
120
CRT015 Carotid Artery Occlusion 43 0.063
121
ART005 Arteriovenous Malformation 65 0.060
122
PRT036 Peritonitis 62 0.060
123
P ENC018 Encephalopathy 59 0.060
124
P INT030 Intracranial Aneurysm 54 0.060
125
ATR060 Atrial Standstill, Digenic 53 0.060
126
VSC047 Vascular Malformation 45 0.060
127
P CRN074 Coronary Artery Aneurysm 44 0.060
128
c PRM225 Primary Thrombocytopenia 42 0.060
129
CPL007 Capillary Malformation-Arteriovenous Malformation 41 0.060
130
HRT012 Heart Valve Disease 41 0.060
131
ALR002 Al-Raqad Syndrome 36 0.060
132
KWS002 Kawasaki Disease 70 0.057
133
ART016 Aortic Aneurysm 67 0.057
134
P CRD011 Cardiomyopathy 67 0.057
135
P HYD006 Hydrocephalus 67 0.057
136
P HYP083 Hypopituitarism 52 0.057
137
P CRV039 Cervicitis 44 0.057
138
CRB085 Cerebral Hemorrhage 43 0.057
139
LMR001 Lemierre's Syndrome 41 0.057
140
PRP080 Peripheral Artery Disease 36 0.057
141
MYT019 May-Thurner Syndrome 23 0.057
142
c CRN174 Coronary Heart Disease 2 22 0.057
143
SRC014 Sarcoma 66 0.054
144
c HMP029 Hemophilia a 64 0.054
145
PLY125 Polycythemia Vera, Somatic 63 0.054
146
FCT007 Factor Vii Deficiency 62 0.054
147
P ESN007 Eosinophilia 61 0.054
148
P THL005 Thalassemia 61 0.054
149
VNW001 Von Willebrand's Disease 61 0.054
150
P NRP001 Neuropathy 60 0.054
151
CHL071 Child Syndrome 58 0.054
152
ART017 Aortic Disease 58 0.054
153
CHL067 Cholecystitis 56 0.054
154
ADL002 Adult Syndrome 53 0.054
155
KDS001 Kid Syndrome 53 0.054
156
TTH006 Tooth Disease 52 0.054
157
SCK005 Sickle Cell Disease 49 0.054
158
HYP063 Hypersplenism 48 0.054
159
c CHR431 Chronic Venous Insufficiency 44 0.054
160
CLP006 Clopidogrel Resistance 39 0.054
161
ABD004 Abdominal Tuberculosis 34 0.054
162
SPH007 Sphenoid Sinusitis 24 0.054
163
P BRS047 Breast Cancer 100 0.050
164
P ART022 Arthritis 75 0.050
165
MYL009 Myelodysplastic Syndrome 74 0.050
166
P APL001 Aplastic Anemia 73 0.050
167
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.050
168
OST017 Osteomyelitis 59 0.050
169
P HMR003 Hemorrhagic Disease 57 0.050
170
HPT019 Hepatic Encephalopathy 56 0.050
171
P HYP076 Hyperthyroidism 56 0.050
172
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.050
173
P HRD011 Hereditary Spherocytosis 53 0.050
174
P PYL005 Pyelonephritis 52 0.050
175
P END033 Endocarditis 52 0.050
176
HRT007 Heart Cancer 50 0.050
177
P AFB001 Afibrinogenemia 46 0.050
178
SPP008 Suppurative Otitis Media 45 0.050
179
P ABD003 Abdominal Aortic Aneurysm 43 0.050
180
THR035 Thrombasthenia 42 0.050
181
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 41 0.050
182
CHR466 Chronic Thromboembolic Pulmonary Hypertension 37 0.050
183
P HRT017 Heart Tumor 35 0.050
184
PLM027 Pulmonary Embolism and Infarction 26 0.050
185
c THR023 Thrombophilia Due to Thrombomodulin Defect 19 0.050
186
c ADL079 Adult Heart Tumor 19 0.050
187
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.046
188
c HPT001 Hepatitis C 68 0.046
189
P PNM007 Pneumonia 66 0.046
190
c HPT016 Hepatitis B 64 0.046
191
c HMP004 Hemophilia B 62 0.046
192
SPN186 Spinal Cord Injury 62 0.046
193
P ASP006 Aspergillosis 60 0.046
194
HYP066 Hyperglycemia 60 0.046
195
RBR001 Roberts Syndrome 59 0.046
196
ORL011 Oral Cancer 55 0.046
197
NWC001 Newcastle Disease 54 0.046
198
INT007 Intermediate Coronary Syndrome 52 0.046
199
BRN106 Burns 52 0.046
200
CHL069 Cholesteatoma 51 0.046
201
THR104 Thrombophilia Due to Antithrombin Iii Deficiency 50 0.046
202
PRP016 Paraplegia 49 0.046
203
BCT015 Bacteremia 48 0.046
204
SPL012 Splenic Disease 47 0.046
205
PRP007 Priapism 47 0.046
206
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.046
207
ACR041 Acromelic Frontonasal Dysostosis 46 0.046
208
SPH001 Sapho Syndrome 44 0.046
209
EXS001 Exostosis 44 0.046
210
BRT030 Birth Defects 43 0.046
211
MDS022 Mediastinitis 41 0.046
212
CTS005 Catastrophic Antiphospholipid Syndrome 41 0.046
213
ERY004 Erysipelas 40 0.046
214
CRB086 Cerebral Aneurysms 39 0.046
215
RTR011 Retroperitoneal Fibrosis 38 0.046
216
P RTN022 Retinal Vein Occlusion 37 0.046
217
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 34 0.046
218
ZYG002 Zygomycosis 33 0.046
219
EYC003 Eye Accommodation Disease 26 0.046
220
HPT081 Hepatic Infarction 24 0.046
221
PTR001 Petrositis 24 0.046
222
c CRN177 Coronary Heart Disease 7 22 0.046
223
c CRN173 Coronary Heart Disease 8 20 0.046
224
c CRN176 Coronary Heart Disease 9 20 0.046
225
THR088 Thrombophilia Due to Protein S Deficiency, Autosomal Recessive 18 0.046
226
CGL001 Coagulation Protein Disease 16 0.046
227
P LNG032 Lung Cancer 94 0.042
228
P MLT019 Multiple Myeloma 80 0.042
229
P PHC003 Pheochromocytoma 71 0.042
230
c HYP595 Hypertension, Essential 69 0.042
231
P LPR003 Leprosy 68 0.042
232
P PLR004 Pleuropulmonary Blastoma 64 0.042
233
HMT002 Hematologic Cancer 64 0.042
234
CRD119 Cardiac Arrest 63 0.042
235
P ESP024 Esophagitis 62 0.042
236
c ACT073 Acute Leukemia 62 0.042
237
BHC003 Behcet Syndrome 61 0.042
238
APP008 Appendicitis 60 0.042
239
P SHR029 Short Syndrome 60 0.042
240
c NPH055 Nephrotic Syndrome, Type 1 59 0.042
241
MRB003 Morbid Obesity 58 0.042
242
SCH014 Schistosomiasis 58 0.042
243
c THR082 Thrombophilia Due to Activated Protein C Resistance 57 0.042
244
PRS047 Prostatitis 56 0.042
245
P MMB011 Membranous Nephropathy 56 0.042
246
KLN001 Klinefelter's Syndrome 55 0.042
247
BLR001 Biliary Atresia 51 0.042
248
c INF071 Inflammatory Bowel Disease 1 51 0.042
249
CRN030 Coronary Stenosis 50 0.042
250
LMB062 Limb Ischemia 48 0.042
251
OCL006 Ocular Hypertension 48 0.042
252
GLC008 Glucose Metabolism Disease 47 0.042
253
ANR004 Anuria 46 0.042
254
CRB004 Cerebral Artery Occlusion 46 0.042
255
c ACT042 Acute Pyelonephritis 46 0.042
256
ALN001 Aland Island Eye Disease 45 0.042
257
TNP003 Tn Polyagglutination Syndrome, Somatic 44 0.042
258
DDN006 Duodenitis 44 0.042
259
SPL018 Splenomegaly 44 0.042
260
CRD001 Cardiac Tamponade 44 0.042
261
CDQ001 Cauda Equina Syndrome 42 0.042
262
PRT019 Protein-Losing Enteropathy 41 0.042
263
BRN080 Brain Ischemia 41 0.042
264
MDY003 Mody, Type Ii 38 0.042
265
LCK001 Locked-in Syndrome 38 0.042
266
c THR037 Thrombocytopenia 2 37 0.042
267
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 35 0.042
268
HMC014 Homocysteinemia 34 0.042
269
c FRN011 Frontal Sinusitis 30 0.042
270
c THR048 Thrombocytopenia 4 29 0.042
271
WRF003 Warfarin Syndrome 28 0.042
272
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 26 0.042
273
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 24 0.042
274
HRD083 Hereditary Antithrombin Deficiency 22 0.042
275
HGH021 Hughes-Stovin Syndrome 18 0.042
276
THN005 Thunderclap Headache 16 0.042
277
ORB016 Orbital Varix 10 0.042
278
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.038
279
GST053 Gastric Cancer 77 0.038
280
TTR001 Tetralogy of Fallot 71 0.038
281
SCK003 Sickle Cell Anemia 68 0.038
282
PCK002 Pick Disease 67 0.038
283
P TRN020 Turner Syndrome 64 0.038
284
GLN010 Glanzmann Thrombasthenia 63 0.038
285
GST092 Gastroesophageal Reflux 61 0.038
286
WST001 West Syndrome 61 0.038
287
WLL001 Williams-Beuren Syndrome 61 0.038
288
TYP007 Typhoid Fever 61 0.038
289
P SLP006 Sleep Apnea 61 0.038
290
P HML002 Hemolytic Anemia 60 0.038
291
FCT006 Factor V Deficiency 60 0.038
292
ADN018 Adenoma 59 0.038
293
LPD008 Lipid Metabolism Disorder 58 0.038
294
P ORL007 Oral Cavity Cancer 58 0.038
295
EXF001 Exfoliation Syndrome 57 0.038
296
WLL006 Wells Syndrome 56 0.038
297
P INT070 Intestinal Obstruction 56 0.038
298
PRT093 Proteus Syndrome, Somatic 55 0.038
299
c ART101 Aortic Valve Disease 2 55 0.038
300
P THY032 Thyroiditis 54 0.038
301
P PRP019 Peripheral Nervous System Disease 54 0.038
302
P LMY004 Leiomyosarcoma 53 0.038
303
RDC002 Radiculopathy 53 0.038
304
PRC013 Pericarditis 52 0.038
305
VRC001 Varicocele 50 0.038
306
PRN021 Paranasal Sinus Disease 50 0.038
307
URM002 Uremia 50 0.038
308
c ACT134 Acute Liver Failure 50 0.038
309
NDL013 Nodular Regenerative Hyperplasia 49 0.038
310
RLP001 Relapsing Polychondritis 49 0.038
311
CHR001 Churg-Strauss Syndrome 49 0.038
312
HLL004 Hellp Syndrome 49 0.038
313
P CHL066 Cholangitis 49 0.038
314
P CMP008 Compartment Syndrome 48 0.038
315
CHL004 Cholelithiasis 48 0.038
316
LPD004 Lipoid Nephrosis 48 0.038
317
BNF002 Bone Fracture 47 0.038
318
CCN002 Cocaine Abuse 47 0.038
319
P PLN008 Peeling Skin Syndrome 47 0.038
320
ACT058 Active Peptic Ulcer Disease 46 0.038
321
FSC004 Fasciitis 46 0.038
322
ISC002 Ischemic Optic Neuropathy 46 0.038
323
GDS001 Good Syndrome 45 0.038
324
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 0.038
325
P CRN035 Cranial Nerve Palsy 43 0.038
326
P RTN014 Retinal Artery Occlusion 43 0.038
327
THL018 Thalassemia Major 42 0.038
328
BCK006 Back Pain 42 0.038
329
NSL022 Nasal Cavity Disease 42 0.038
330
ACT055 Actinomycosis 41 0.038
331
GST071 Gastrointestinal Carcinoma 41 0.038
332
BLD054 Blood Protein Disease 40 0.038
333
SCR015 Scarlet Fever 39 0.038
334
BRS090 Breast Reconstruction 39 0.038
335
STR044 Steroid-Resistant Nephrotic Syndrome 38 0.038
336
IMP003 Impaired Renal Function Disease 37 0.038
337
INF013 Inferior Myocardial Infarction 37 0.038
338
SPN185 Spinal Cord Infarction 36 0.038
339
CRT012 Cortical Blindness 36 0.038
340
c CNT016 Central Retinal Vein Occlusion 35 0.038
341
INT010 Intracranial Embolism 35 0.038
342
CRB031 Cerebral Arterial Disease 31 0.038
343
SBD001 Subdural Empyema 30 0.038
344
THR068 Thrombophilia Due to Protein C Deficiency, Autosomal Recessive 26 0.038
345
SNG003 Single Ventricular Heart 24 0.038
346
VNF001 Vein of Galen Aneurysm 22 0.038
347
c CRN172 Coronary Heart Disease 3 21 0.038
348
THR089 Thrombophilia Due to Protein S Deficiency, Autosomal Dominant 20 0.038
349
THR067 Thrombophilia Due to Protein C Deficiency, Autosomal Dominant 20 0.038
350
ABD009 Abducens Palsy 18 0.038
351
WSC001 Wisconsin Syndrome 17 0.038
352
P ACT061 Acute Sphenoidal Sinusitis 14 0.038
353
P CLR023 Colorectal Cancer 97 0.033
354
P PNC035 Pancreatic Cancer 85 0.033
355
P OVR042 Ovarian Cancer 75 0.033
356
CMP005 Campomelic Dysplasia 72 0.033
357
c HPT073 Hepatitis C Virus 72 0.033
358
CNG034 Congestive Heart Failure 71 0.033
359
P CLC005 Celiac Disease 67 0.033
360
DWN001 Down Syndrome 65 0.033
361
P CNJ013 Conjunctivitis 65 0.033
362
BRC012 Brucellosis 65 0.033
363
P BCL006 B-Cell Lymphomas 64 0.033
364
P PSR002 Psoriasis 63 0.033
365
RSP006 Respiratory System Disease 62 0.033
366
P ENC004 Encephalitis 61 0.033
367
P LYM025 Lymphedema 61 0.033
368
P INT068 Intestinal Disease 61 0.033
369
P GRV001 Graves' Disease 61 0.033
370
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 61 0.033
371
P MYM002 Moyamoya Disease 60 0.033
372
P TMP003 Temporal Arteritis 60 0.033
373
P GST049 Gastrointestinal System Cancer 60 0.033
374
c ATM010 Autoimmune Hemolytic Anemia 60 0.033
375
SPT004 Septic Arthritis 59 0.033
376
c HPT003 Hepatitis a 59 0.033
377
P MTR012 Mitral Valve Disease 59 0.033
378
c FML001 Familial Atrial Fibrillation 59 0.033
379
LYM021 Lymphadenitis 58 0.033
380
RHB003 Rhabdomyosarcoma 58 0.033
381
PHR003 Pharyngitis 58 0.033
382
TRN015 Transient Cerebral Ischemia 56 0.033
383
PLS011 Plasmacytoma 56 0.033
384
INT079 Intrahepatic Cholangiocarcinoma 55 0.033
385
PMS001 Poems Syndrome 55 0.033
386
CRT016 Carotid Artery Disease 55 0.033
387
HYP266 Hypoxia 55 0.033
388
c PND001 Pain Disorder 55 0.033
389
BLD034 Bile Duct Carcinoma 55 0.033
390
GST050 Gastrointestinal System Disease 54 0.033
391
HYP080 Hypogonadism 54 0.033
392
P EXP004 Exophthalmos 54 0.033
393
LYM040 Lymphoblastic Lymphoma 54 0.033
394
HMP005 Hemiplegia 54 0.033
395
BRG013 Buerger Disease 53 0.033
396
LYM019 Lymphosarcoma 53 0.033
397
ESP023 Esophageal Disease 53 0.033
398
BNM001 Bone Marrow Cancer 52 0.033
399
CRH005 Crohn's Colitis 52 0.033
400
BRN071 Brain Injury 52 0.033
401
P PNC001 Pancytopenia 52 0.033
402
NRT004 Neuritis 52 0.033
403
CRN036 Craniopharyngioma 52 0.033
404
GST040 Gastric Adenocarcinoma 52 0.033
405
CHC001 Chickenpox 52 0.033
406
P PRT096 Peritoneal Mesothelioma 51 0.033
407
c INF067 Inflammatory Bowel Disease 10 51 0.033
408
BRN004 Brain Edema 51 0.033
409
MCN001 Mucinous Adenocarcinoma 50 0.033
410
STM006 Stomach Disease 50 0.033
411
INT253 Intestinal Benign Neoplasm 50 0.033
412
PYD001 Pyoderma Gangrenosum 49 0.033
413
PYD002 Pyoderma 49 0.033
414
CMR002 Coumarin Resistance 48 0.033
415
ACT017 Acute Chest Syndrome 48 0.033
416
MCR088 Microscopic Polyangiitis 48 0.033
417
OPT009 Optic Neuritis 48 0.033
418
MYL001 Myelitis 48 0.033
419
SXL003 Sexual Disorder 47 0.033
420
SYN036 Syncope 47 0.033
421
P RNV001 Renovascular Hypertension 47 0.033
422
SPN035 Spindle Cell Sarcoma 47 0.033
423
HST009 Histiocytoma 47 0.033
424
SDD007 Sudden Cardiac Death 46 0.033
425
CHR074 Choriocarcinoma 46 0.033
426
P TRC086 Trichohepatoenteric Syndrome 1 46 0.033
427
ART004 Aortic Atherosclerosis 46 0.033
428
ANG018 Angiomyolipoma 46 0.033
429
PLV005 Pelviureteric Junction Obstruction 45 0.033
430
HPT046 Hepatic Veno-Occlusive Disease 45 0.033
431
ESP002 Esophageal Varix 44 0.033
432
PHY002 Physical Disorder 44 0.033
433
EBS001 Ebstein Anomaly 44 0.033
434
ESN011 Eisenmenger Syndrome 44 0.033
435
HYD057 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 44 0.033
436
HYD012 Hydrops Fetalis 44 0.033
437
VTM002 Vitamin B12 Deficiency 44 0.033
438
CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 43 0.033
439
MYH001 May-Hegglin Anomaly 43 0.033
440
TRC023 Trichinosis 43 0.033
441
GND003 Gonadal Disease 43 0.033
442
ART031 Aortic Coarctation 42 0.033
443
c INF069 Infantile Neuroaxonal Dystrophy 1 42 0.033
444
VGN023 Vaginitis 42 0.033
445
P ERY048 Erythrocytosis, Familial, 2 42 0.033
446
NRN002 Neuronitis 42 0.033
447
PNM013 Pneumococcal Meningitis 41 0.033
448
WTH001 Withdrawal Disorder 41 0.033
449
MCR225 Macrophage Activation Syndrome 40 0.033
450
SXD001 Sex Differentiation Disease 40 0.033
451
SPC003 Specific Developmental Disorder 40 0.033
452
P LBY004 Labyrinthitis 40 0.033
453
SPR007 Superior Mesenteric Artery Syndrome 39 0.033
454
TRN012 Transient Global Amnesia 39 0.033
455
SHW001 Shwartzman Phenomenon 37 0.033
456
P CHR084 Chromosomal Disease 37 0.033
457
INT221 Intravascular Large B-Cell Lymphoma 36 0.033
458
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 36 0.033
459
c PLN018 Peeling Skin Syndrome 2 35 0.033
460
BSL004 Basilar Artery Occlusion 35 0.033
461
P ACT080 Acute Pulmonary Heart Disease 32 0.033
462
EPD005 Epidural Abscess 32 0.033
463
c TRC078 Trichohepatoenteric Syndrome 2 31 0.033
464
c THR102 Thrombocytopenia 5 30 0.033
465
c CHR036 Chronic Cholangitis 27 0.033
466
c RNL016 Renal Infectious Disease 24 0.033
467
MND006 Mondor Disease 21 0.033
468
DBL009 Double Inferior Vena Cava 19 0.033
469
THR007 Thrombophlebitis Migrans 18 0.033
470
ACT174 Acute Peripheral Arterial Occlusion 17 0.033
471
PRN017 Perianal Hematoma 15 0.033
472
NNT044 Neonatal Antiphospholipid Syndrome 15 0.033
473
c ANT041 Antiphospholipid Syndrome, Familial 15 0.033
474
HRD147 Hereditary Thrombophilia Due to Congenital Protein S Deficiency 11 0.033
475
P RHM011 Rheumatoid Arthritis 88 0.027
476
CYS001 Cystic Fibrosis 86 0.027
477
P MDL005 Medulloblastoma 77 0.027
478
c CHR090 Chronic Lymphocytic Leukemia 74 0.027
479
MNT001 Mantle Cell Lymphoma 70 0.027
480
c NRF018 Neurofibromatosis, Type 1 68 0.027
481
SKN016 Skin Disease 68 0.027
482
P KDN017 Kidney Cancer 67 0.027
483
P MYP004 Myopathy 67 0.027
484
c PNC108 Pancreatitis, Hereditary 67 0.027
485
c CHR089 Chronic Kidney Failure 66 0.027
486
OBS061 Obstructive Sleep Apnea 66 0.027
487
OBS002 Obsessive-Compulsive Disorder 66 0.027
488
BRK010 Burkitt Lymphoma 66 0.027
489
P AST007 Astrocytoma 65 0.027
490
P HYP117 Hypertriglyceridemia 65 0.027
491
P HYP086 Hypothyroidism 65 0.027
492
P MSC005 Muscular Dystrophy 64 0.027
493
P ALX003 Alexander Disease 64 0.027
494
MTH009 Mouth Disease 63 0.027
495
ATP002 Atopy 63 0.027
496
P ART023 Arthropathy 63 0.027
497
P ANR007 Anorexia Nervosa 63 0.027
498
LPT001 Leptospirosis 63 0.027
499
LNG099 Lung Disease 62 0.027
500
P EHL001 Ehlers-Danlos Syndrome 61 0.027
501
DRM006 Dermatitis 61 0.027
502
TXC005 Toxic Shock Syndrome 61 0.027
503
HYP056 Hypoglycemia 61 0.027
504
c VRL010 Viral Hepatitis 61 0.027
505
CNN005 Connective Tissue Disease 61 0.027
506
P HMN010 Hemangioma 60 0.027
507
GNG013 Gingivitis 60 0.027
508
ADM013 Adamantinoma of Long Bones 59 0.027
509
P FCL005 Focal Segmental Glomerulosclerosis 59 0.027
510
P HYP060 Hyperinsulinism 59 0.027
511
c SYS004 Systemic Mastocytosis 59 0.027
512
P ANP001 Anaplastic Large Cell Lymphoma 58 0.027
513
TNS005 Tonsillitis 58 0.027
514
P CTR002 Cataract 57 0.027
515
PNC034 Pancreas Disease 57 0.027
516
MLG056 Malignant Hyperthermia 57 0.027
517
CTS003 Coats Disease 57 0.027
518
ADL030 Adult-Onset Still's Disease 57 0.027
519
P THR003 Thoracic Aortic Aneurysm 57 0.027
520
P RBL001 Rubella 56 0.027
521
PLM010 Pulmonary Edema 56 0.027
522
P OVR049 Ovarian Disease 55 0.027
523
CHL127 Cholangiocarcinoma, Susceptibility to 55 0.027
524
CRB037 Cerebral Palsy 54 0.027
525
c BCT007 Bacterial Meningitis 54 0.027
526
MVM001 Movement Disease 54 0.027
527
P ECL001 Eclampsia 54 0.027
528
P HYP620 Hypoprothrombinemia 54 0.027
529
KLP010 Klippel-Trenaunay-Weber Syndrome 54 0.027
530
P MST009 Mastocytosis 54 0.027
531
P MYC008 Myocarditis 54 0.027
532
P END044 Endometriosis 53 0.027
533
URN009 Urinary System Disease 53 0.027
534
ALL026 Allergic Hypersensitivity Disease 53 0.027
535
ECH003 Echinococcosis 53 0.027
536
PLV003 Pelvic Inflammatory Disease 53 0.027
537
P DBT005 Diabetes Insipidus 53 0.027
538
c ART115 Aortic Valve Disease 1 53 0.027
539
P GND004 Gonadal Dysgenesis 53 0.027
540
DBN001 Dubin-Johnson Syndrome 52 0.027
541
TRM010 Traumatic Brain Injury 52 0.027
542
c HPT015 Hepatitis D 52 0.027
543
END030 End Stage Renal Failure 52 0.027
544
P CRV031 Cervical Adenocarcinoma 52 0.027
545
P URF003 Urofacial Syndrome 1 52 0.027
546
P NNT009 Neonatal Diabetes Mellitus 52 0.027
547
P PRM006 Primary Biliary Cirrhosis 52 0.027
548
ALV002 Alveolar Echinococcosis 51 0.027
549
ERD001 Erdheim-Chester Disease 51 0.027
550
P PLY041 Polymyositis 51 0.027
551
ASP003 Aseptic Meningitis 51 0.027
552
VSC044 Visceral Myopathy 51 0.027
553
LRN003 Learning Disability 51 0.027
554
RHM028 Rheumatic Heart Disease 51 0.027
555
P FML035 Familial Hyperlipidemia 50 0.027
556
P LPS002 Liposarcoma 50 0.027
557
P OVR046 Ovarian Cyst 50 0.027
558
QBC001 Quebec Platelet Disorder 50 0.027
559
PRC012 Pericardial Effusion 50 0.027
560
FCL012 Facial Paralysis 50 0.027
561
c ACT071 Acute Kidney Failure 50 0.027
562
MGC001 Megacolon 50 0.027
563
PMP001 Pemphigus 49 0.027
564
END031 Endometrial Stromal Sarcoma 49 0.027
565
GSG001 Gas Gangrene 49 0.027
566
P SHR001 Short Bowel Syndrome 48 0.027
567
FML039 Female Reproductive System Disease 48 0.027
568
OBS001 Obstructive Jaundice 48 0.027
569
P APL006 Aplasia Cutis Congenita 48 0.027
570
UPP004 Upper Respiratory Tract Disease 48 0.027
571
P HMR005 Hemorrhoid 48 0.027
572
HND003 Hand-Foot-Uterus Syndrome 47 0.027
573
HYD002 Hydronephrosis 47 0.027
574
c MLG069 Malignant Hypertension 47 0.027
575
P ENC008 Encephalocele 47 0.027
576
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 47 0.027
577
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 47 0.027
578
MXD023 Mixed Cell Type Cancer 47 0.027
579
P SYR001 Syringomyelia 47 0.027
580
CRY004 Cryoglobulinemia 47 0.027
581
PRM020 Premenstrual Tension 46 0.027
582
RPR002 Reproductive System Disease 46 0.027
583
P PRD008 Periodontitis 46 0.027
584
PRN011 Pernicious Anemia 46 0.027
585
P END047 Endophthalmitis 46 0.027
586
CVR006 Cavernous Hemangioma 46 0.027
587
ADN027 Adenomyosis 46 0.027
588
MNN009 Meningoencephalitis 45 0.027
589
c MLG002 Malignant Peritoneal Mesothelioma 45 0.027
590
URT010 Ureteral Obstruction 45 0.027
591
SGN002 Signet Ring Cell Adenocarcinoma 45 0.027
592
NCR007 Necrotizing Fasciitis 45 0.027
593
CLL002 Collecting Duct Carcinoma 45 0.027
594
ALX001 Alexia 45 0.027
595
DDN010 Duodenum Cancer 44 0.027
596
P HRN001 Horner's Syndrome 44 0.027
597
c HMG003 Hemoglobin E Disease 44 0.027
598
PRS045 Prostatic Hypertrophy 44 0.027
599
OCL069 Ocular Motor Apraxia 44 0.027
600
GLM011 Glomerulosclerosis 44 0.027
601
SND002 Sneddon Syndrome 44 0.027
602
SPL004 Splenic Marginal Zone Lymphoma 43 0.027
603
PRM025 Primary Bacterial Infectious Disease 43 0.027
604
FCT008 Factitious Disorder 43 0.027
605
EVN001 Evans' Syndrome 43 0.027
606
SMN007 Seminoma 42 0.027
607
NRR001 Neuroretinitis 42 0.027
608
HPT008 Hepatic Tuberculosis 42 0.027
609
P PRP034 Purpura Fulminans 42 0.027
610
CNV002 Conversion Disorder 42 0.027
611
c ACQ014 Acquired Hemophilia 42 0.027
612
FBR019 Fibromatosis 42 0.027
613
HPT067 Hepatocellular Adenoma 42 0.027
614
LMY003 Leiomyomatosis 41 0.027
615
STR077 Streptococcal Toxic-Shock Syndrome 41 0.027
616
TRN007 Transsexualism 41 0.027
617
CNN002 Cannabis Abuse 41 0.027
618
HST016 Histiocytic Sarcoma 40 0.027
619
CYS009 Cystadenoma 40 0.027
620
SCT001 Sciatic Neuropathy 40 0.027
621
c INH004 Inherited Blood Coagulation Disease 39 0.027
622
BRN026 Branch Retinal Artery Occlusion 39 0.027
623
NTR005 Nutritional Deficiency Disease 39 0.027
624
P PRX010 Paroxysmal Ventricular Fibrillation 39 0.027
625
PRL008 Paralytic Ileus 39 0.027
626
P MXL015 Maxillary Sinusitis 38 0.027
627
P ATM020 Autoimmune Enteropathy 38 0.027
628
LYM005 Lymphocele 38 0.027
629
ESN020 Eosinophilic Granulomatosis with Polyangiitis 38 0.027
630
HMN016 Hemangioendothelioma 38 0.027
631
CRT013 Carotid Stenosis 37 0.027
632
PLM013 Pulmonary Immaturity 37 0.027
633
NNT024 Neonatal Stroke 37 0.027
634
SBS006 Sebastian Syndrome 37 0.027
635
ALC005 Alcoholic Pancreatitis 36 0.027
636
LYM014 Lymphangitis 36 0.027
637
CPL011 Capillary Malformations, Congenital, 1, Somatic, Mosaic 35 0.027
638
OBS004 Obstructive Hydrocephalus 35 0.027
639
c CNT028 Central Retinal Artery Occlusion 35 0.027
640
ERY045 Erythrocytosis, Somatic 35 0.027
641
HRS011 Horseshoe Kidney 35 0.027
642
TTL010 Total Anomalous Pulmonary Venous Return 35 0.027
643
c SBC003 Subacute Bacterial Endocarditis 35 0.027
644
LNG095 Lung Abscess 34 0.027
645
CNS002 Constrictive Pericarditis 34 0.027
646
c DYS165 Dysfibrinogenemia, Congenital 34 0.027
647
MSN003 Mesenteric Vascular Occlusion 34 0.027
648
FRN014 Fournier Gangrene 34 0.027
649
c PLN017 Peeling Skin Syndrome 1 33 0.027
650
BLR027 Blue Rubber Bleb Nevus 33 0.027
651
PLX004 Plexopathy 33 0.027
652
ETH009 Ethmoid Sinusitis 33 0.027
653
GNT005 Giant Hemangioma 33 0.027
654
PRN039 Paraneoplastic Syndromes 33 0.027
655
SRN001 Serine Deficiency 32 0.027
656
c ACT036 Acute Cholangitis 32 0.027
657
CHL070 Cholesterol Embolism 32 0.027
658
MYS004 Myiasis 31 0.027
659
c PLN021 Peeling Skin Syndrome 3 31 0.027
660
BWN006 Bowen's Disease 31 0.027
661
WDS002 Woods Syndrome 30 0.027
662
HNS001 Hansen's Disease 29 0.027
663
TXC001 Toxic Megacolon 28 0.027
664
DNT046 Dental Abscess 27 0.027
665
GLY032 Glycosylphosphatidylinositol Deficiency 27 0.027
666
PRM008 Parametritis 27 0.027
667
MLK004 Malakoplakia 27 0.027
668
BRW006 Brown Syndrome 26 0.027
669
YNG002 Young Syndrome 26 0.027
670
FBR028 Fibrosing Mediastinitis 24 0.027
671
c INF078 Inflammatory Bowel Disease 2 24 0.027
672
MNN005 Meningovascular Neurosyphilis 24 0.027
673
CRB087 Cerebral Arteriosclerosis 24 0.027
674
NRS005 Neurosarcoidosis 23 0.027
675
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 23 0.027
676
VSC009 Vascular Skin Disease 22 0.027
677
CVR001 Cavernous Sinus Meningioma 22 0.027
678
MTH044 Mthfr Gene Mutation 22 0.027
679
ATR024 Atrial Fibrillation and Stroke 22 0.027
680
WND002 Wandering Spleen 20 0.027
681
PRX023 Paroxysmal Nocturnal Hemoglobinuria, Somatic 20 0.027
682
c ACT035 Acute Frontal Sinusitis 19 0.027
683
THR020 Thrombophilia Due to Heparin Cofactor Ii Deficiency 19 0.027
684
FMR002 Femoral Cancer 19 0.027
685
NVS004 Nova Syndrome 19 0.027
686
THR021 Thrombophilia Due to Hrg Deficiency 17 0.027
687
PRP050 Peripheral Arterial Occlusive Disease 1 17 0.027
688
c BLR016 Biliary Cirrhosis, Primary, 2 17 0.027
689
HMC030 Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency 17 0.027
690
AND005 Androgen Insensitivity Syndrome, Mild 16 0.027
691
CRT056 Carotidynia 16 0.027
692
c BLR026 Biliary Cirrhosis, Primary, 5 15 0.027
693
CRD023 Cardiomyopathy Cataract Hip Spine Disease 15 0.027
694
OCL024 Ocular Neuromyotonia 13 0.027
695
P PRS040 Prostate Cancer 89 0.019
696
HV1006 Hiv-1 82 0.019
697
P OST012 Osteoarthritis 82 0.019
698
DCH001 Duchenne Muscular Dystrophy 80 0.019
699
P HNT016 Huntington Disease 80 0.019
700
MLR004 Malaria 79 0.019
701
P HYP607 Hypercholesterolemia, Familial 77 0.019
702
ADN021 Adenomatous Polyposis Coli 76 0.019
703
c DLT002 Dilated Cardiomyopathy 75 0.019
704
ESP021 Esophageal Cancer 75 0.019
705
P INF038 Influenza 74 0.019
706
HDG012 Hodgkin Lymphoma 73 0.019
707
c FNC027 Fanconi Anemia, Complementation Group a 73 0.019
708
P WSK001 Wiskott-Aldrich Syndrome 72 0.019
709
P HMC003 Hemochromatosis 72 0.019
710
WLS001 Wilson Disease 72 0.019
711
c LKM061 Leukemia, Acute Myeloid 71 0.019
712
P HRD008 Hereditary Hemorrhagic Telangiectasia 71 0.019
713
P NRV007 Nervous System Disease 71 0.019
714
PTZ001 Peutz-Jeghers Syndrome 70 0.019
715
CRZ001 Crouzon Syndrome 70 0.019
716
TST021 Testicular Germ Cell Tumor 70 0.019
717
FBR012 Fabry Disease 69 0.019
718
P NRB001 Neuroblastoma 69 0.019
719
P DMN001 Diamond-Blackfan Anemia 68 0.019
720
SVR004 Severe Combined Immunodeficiency 68 0.019
721
PLM001 Pulmonary Tuberculosis 68 0.019
722
BCK001 Becker Muscular Dystrophy 68 0.019
723
P OST005 Osteogenesis Imperfecta 67 0.019
724
MLD001 Melioidosis 67 0.019
725
BLD087 Bladder Cancer, Somatic 67 0.019
726
CNT098 Central Core Disease 66 0.019
727
P PLY011 Polycystic Ovary Syndrome 66 0.019
728
P GLB002 Glioblastoma 66 0.019
729
P LYM007 Lymphangioleiomyomatosis 65 0.019
730
P HRP006 Herpes Simplex 65 0.019
731
P PRM019 Premature Ovarian Failure 64 0.019
732
P AMY004 Amyloidosis 64 0.019
733
P CRB042 Cerebellar Ataxia 64 0.019
734
P CSH001 Cushing's Syndrome 64 0.019
735
P DYS007 Dyskeratosis Congenita 63 0.019
736
PNC041 Pancreatic Ductal Adenocarcinoma 63 0.019
737
P SPN046 Spinal Muscular Atrophy 63 0.019
738
P PRD006 Prader-Willi Syndrome 63 0.019
739
GLL018 Gallbladder Cancer 63 0.019
740
P SPN301 Spinocerebellar Ataxia 2 63 0.019
741
P LNG064 Lung Cancer Susceptibility 3 62 0.019
742
P NRV006 Nervous System Cancer 62 0.019
743
P ATP001 Atopic Dermatitis 62 0.019
744
P PRT010 Parathyroid Carcinoma 62 0.019
745
FCT003 Factor X Deficiency 62 0.019
746
GLB015 Glioblastoma Multiforme 62 0.019
747
P ADD001 Addison's Disease 62 0.019
748
WGN006 Wegener Granulomatosis 62 0.019
749
OCL009 Ocular Cancer 62 0.019
750
PRM097 Primary Immunodeficiency Disease 61 0.019
751
ORN006 Ornithine Transcarbamylase Deficiency 61 0.019
752
LSC001 Lesch-Nyhan Syndrome 61 0.019
753
P INF032 Infertility 61 0.019
754
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 60 0.019
755
c MCR115 Microvascular Complications of Diabetes 5 60 0.019
756
HRY003 Hairy Cell Leukemia 60 0.019
757
DRM014 Dermatofibrosarcoma Protuberans 60 0.019
758
GST045 Gastroenteritis 60 0.019
759
P RTN025 Retinoschisis 59 0.019
760
P VNT002 Ventricular Septal Defect 59 0.019
761
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.019
762
P UVT001 Uveitis 59 0.019
763
CHY002 Chylomicron Retention Disease 59 0.019
764
P NTR004 Neutropenia 59 0.019
765
LGN002 Legionellosis 59 0.019
766
STT001 Status Epilepticus 59 0.019
767
P PLC011 Pilocytic Astrocytoma 58 0.019
768
P MCR010 Microcephaly 58 0.019
769
P GST044 Gastritis 58 0.019
770
P DRM010 Dermatomyositis 58 0.019
771
P GLM045 Glioma 58 0.019
772
P PRP029 Porphyria 58 0.019
773
CRT002 Cartilage-Hair Hypoplasia 58 0.019
774
ARG002 Argininosuccinic Aciduria 57 0.019
775
RHM027 Rheumatic Disease 57 0.019
776
ING001 Inguinal Hernia 57 0.019
777
NRM005 Neuromuscular Disease 57 0.019
778
P MCR129 Microvascular Complications of Diabetes 1 57 0.019
779
P INT143 Interstitial Cystitis 57 0.019
780
P CHN012 Chondrosarcoma 57 0.019
781
c ACT210 Acute Respiratory Distress Syndrome 57 0.019
782
P SZR006 Seizure Disorder 57 0.019
783
STR026 Star Syndrome 56 0.019
784
P SCL018 Scoliosis 56 0.019
785
P PRM002 Primary Hyperoxaluria 56 0.019
786
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 56 0.019
787
SFT003 Soft Tissue Sarcoma 56 0.019
788
CND002 Conduct Disorder 56 0.019
789
JNT002 Joint Disorders 56 0.019
790
RTN018 Retinal Disease 56 0.019
791
P MYS005 Myositis 56 0.019
792
P PTS002 Ptosis 56 0.019
793
HRP004 Herpes Zoster 56 0.019
794
P AVS004 Avascular Necrosis of the Femoral Head 56 0.019
795
INT002 Intermittent Claudication 56 0.019
796
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 55 0.019
797
c OST135 Osteogenesis Imperfecta, Type I 55 0.019
798
CHL014 Cholera 55 0.019
799
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 55 0.019
800
CHN016 Cohen Syndrome 55 0.019
801
P PLY017 Polyarteritis Nodosa 55 0.019
802
GST023 Gastric Ulcer 55 0.019
803
PNC033 Pancreas Adenocarcinoma 55 0.019
804
P HST010 Histiocytosis 55 0.019
805
P MNC007 Monocytic Leukemia 55 0.019
806
CCC001 Coccidioidomycosis 55 0.019
807
P ACT074 Acute Lymphocytic Leukemia 55 0.019
808
RCT018 Rectal Neoplasm 55 0.019
809
c MLG054 Malignant Histiocytosis 55 0.019
810
P PLY006 Polydactyly 55 0.019
811
P OLG002 Oligodendroglioma 55 0.019
812
P HMR012 Hemorrhagic Fever 55 0.019
813
SCR008 Scrub Typhus 54 0.019
814
BRN038 Bronchial Disease 54 0.019
815
MNT002 Mental Depression 54 0.019
816
NRN004 Neuroendocrine Tumor 54 0.019
817
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.019
818
JPN002 Japanese Encephalitis 54 0.019
819
P SML016 Small Intestine Cancer 54 0.019
820
MCN017 Meconium Ileus 54 0.019
821
c AFB002 Afibrinogenemia, Congenital 54 0.019
822
FDL002 Food Allergy 54 0.019
823
LTT002 Letterer-Siwe Disease 54 0.019
824
GTR002 Goiter 54 0.019
825
BLM002 Bulimia Nervosa 54 0.019
826
c MLG077 Malignant Peripheral Nerve Sheath Tumor 53 0.019
827
GST037 Gastroparesis 53 0.019
828
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.019
829
APH002 Aphasia 53 0.019
830
PTT046 Pituitary Hormone Deficiency, Combined, 2 53 0.019
831
P INT063 Intellectual Disability 53 0.019
832
P STR020 Strabismus 53 0.019
833
ART002 Arts Syndrome 53 0.019
834
C3D001 C3 Deficiency 53 0.019
835
SLP005 Sleep Disorder 53 0.019
836
DNY001 Denys-Drash Syndrome 53 0.019
837
MST016 Mesothelioma, Somatic 53 0.019
838
P ATX004 Ataxia 53 0.019
839
P SYP003 Syphilis 53 0.019
840
HPT022 Hepatoblastoma 53 0.019
841
DRG003 Drug Dependence 53 0.019
842
P ANG015 Angioedema 53 0.019
843
PTT049 Pituitary Adenoma, Acth-Secreting 53 0.019
844
GST063 Gastric Cancer Risk After H. Pylori Infection 53 0.019
845
END035 Endocrine Gland Cancer 52 0.019
846
LYS002 Lysosomal Storage Disease 52 0.019
847
NTH001 Netherton Syndrome 52 0.019
848
HYP291 Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia 52 0.019
849
ANK001 Ankylosis 52 0.019
850
TLN003 Telangiectasis 52 0.019
851
P TRT010 Teratoma 52 0.019
852
IMP002 Imperforate Anus 52 0.019
853
QDR001 Quadriplegia 52 0.019
854
UTR024 Uterine Carcinosarcoma 52 0.019
855
BLR007 Biliary Tract Neoplasm 52 0.019
856
c ACT009 Acute Monocytic Leukemia 52 0.019
857
P ERY008 Erythromelalgia 52 0.019
858
SRS001 Serous Cystadenocarcinoma 52 0.019
859
CYS005 Cysticercosis 52 0.019
860
ART001 Arterial Tortuosity Syndrome 52 0.019
861
FRB001 Farber Lipogranulomatosis 51 0.019
862
CYS010 Cystinosis 51 0.019
863
MCN007 Meconium Aspiration Syndrome 51 0.019
864
P MSC003 Muscular Atrophy 51 0.019
865
P FNC026 Fanconi Renotubular Syndrome 1 51 0.019
866
P HYP071 Hypersensitivity Reaction Type Ii Disease 51 0.019
867
CRT049 Critical Limb Ischemia 51 0.019
868
CCT002 Cicatricial Pemphigoid 51 0.019
869
c PRM012 Primary Polycythemia 51 0.019
870
AMN001 Amenorrhea 51 0.019
871
c LRG001 Large Cell Carcinoma 51 0.019
872
OPT006 Optic Nerve Disease 51 0.019
873
HPT074 Hepatic Adenoma, Somatic 51 0.019
874
CLR109 Colorectal Adenocarcinoma 50 0.019
875
CLN019 Colonic Disease 50 0.019
876
PNN001 Panniculitis 50 0.019
877
RNL024 Renal Glucosuria 50 0.019
878
LYM024 Lymphatic System Disease 50 0.019
879
IMM136 Immune System Disease 50 0.019
880
GLL032 Galloway-Mowat Syndrome 50 0.019
881
SCT005 Scott Syndrome 50 0.019
882
RNL007 Renal Tubular Acidosis 50 0.019
883
MYL020 Myelomeningocele 50 0.019
884
INF034 Infective Endocarditis 50 0.019
885
PRP021 Peripheral Nervous System Neoplasm 50 0.019
886
RTN020 Retinal Vascular Disease 50 0.019
887
PLC005 Placental Insufficiency 50 0.019
888
P RST002 Restrictive Cardiomyopathy 50 0.019
889
MCR004 Macroglobulinemia 50 0.019
890
VNW005 Von Willebrand Disease, Type 1 50 0.019
891
MGR028 Migraine with or Without Aura 1 50 0.019
892
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 49 0.019
893
CLN015 Colon Adenocarcinoma 49 0.019
894
SCH002 Schnitzler Syndrome 49 0.019
895
P CLL015 Collagen Disease 49 0.019
896
LPR001 Lepromatous Leprosy 49 0.019
897
PPL002 Papillary Carcinoma 49 0.019
898
CNG028 Congenital Hypoplastic Anemia 49 0.019
899
P PNV001 Panuveitis 49 0.019
900
P CRP007 Carpenter Syndrome 49 0.019
901
BRK001 Brooke-Spiegler Syndrome 49 0.019
902
EXT010 Extramedullary Plasmacytoma 49 0.019
903
P CHR345 Chronic Pain 49 0.019
904
ILT001 Ileitis 49 0.019
905
c INH020 Inherited Metabolic Disorder 49 0.019
906
GRW007 Growth Hormone Deficiency 48 0.019
907
c HTR008 Heterotaxy, Visceral, 5 48 0.019
908
LBL001 Lobular Neoplasia 48 0.019
909
ALC009 Alcoholic Liver Cirrhosis 48 0.019
910
KMR001 Kimura Disease 48 0.019
911
CRN027 Corneal Neovascularization 48 0.019
912
P TRN034 Transverse Myelitis 48 0.019
913
JCB001 Jacobsen Syndrome 48 0.019
914
GLT021 Glutaricaciduria, Type I 48 0.019
915
RFL001 Reflex Sympathetic Dystrophy 48 0.019
916
PLS009 Plasma Cell Neoplasm 48 0.019
917
MTN003 Motion Sickness 48 0.019
918
CGN006 Cogan Syndrome 48 0.019
919
PPL018 Papillary Adenocarcinoma 48 0.019
920
CHL061 Childhood Leukemia 48 0.019
921
PLN006 Poland Syndrome 48 0.019
922
P ADM011 Adams-Oliver Syndrome 48 0.019
923
WHP001 Whipple Disease 48 0.019
924
c INV001 Invasive Aspergillosis 47 0.019
925
P RNL015 Renal Hypertension 47 0.019
926
P PRM108 Primary Progressive Multiple Sclerosis 47 0.019
927
P GRN010 Granular Cell Tumor 47 0.019
928
DVR002 Diverticulitis 47 0.019
929
P SCL009 Sclerosing Cholangitis 47 0.019
930
PLC007 Placental Abruption 47 0.019
931
c HMG001 Hemoglobin C Disease 47 0.019
932
CRS005 Crest Syndrome 47 0.019
933
DFF036 Differentiated Thyroid Carcinoma 47 0.019
934
PRT029 Parathyroid Adenoma 47 0.019
935
TRN044 Transposition of the Great Arteries 47 0.019
936
PSD007 Pseudomyxoma Peritonei 47 0.019
937
INT067 Interstitial Nephritis 47 0.019
938
GST060 Gastric Cancer, Somatic 47 0.019
939
PNC013 Pancreatic Ductal Carcinoma 47 0.019
940
HNC001 Henoch-Schoenlein Purpura 47 0.019
941
P BRN120 Bronchus Cancer 46 0.019
942
SPC010 Speech and Communication Disorders 46 0.019
943
P PLM025 Pulmonary Venoocclusive Disease 46 0.019
944
TBR011 Tuberculous Meningitis 46 0.019
945
HPT014 Hepatorenal Syndrome 46 0.019
946
c AMY087 Amyloidosis, Hereditary, Transthyretin-Related 46 0.019
947
CYS014 Cystadenocarcinoma 46 0.019
948
SNS023 Sensory System Cancer 46 0.019
949
IDP033 Idiopathic Edema 45 0.019
950
OST003 Osteonecrosis 45 0.019
951
RFR010 Refractory Anemia 45 0.019
952
MTR003 Mitral Valve Stenosis 45 0.019
953
c GRV008 Graves Disease 1 45 0.019
954
DPH021 Diaphragm Disease 45 0.019
955
P VGN017 Vaginal Cancer 45 0.019
956
BNC003 Bone Cancer 45 0.019
957
P MLG086 Malignant Hyperthermia Susceptibility 45 0.019
958
SML036 Small Intestinal Adenocarcinoma 45 0.019
959
CLS010 Cluster Headache 45 0.019
960
EPT020 Epithelioid Hemangioendothelioma 45 0.019
961
CHR288 Chronic Recurrent Multifocal Osteomyelitis 45 0.019
962
VGN020 Vaginal Disease 45 0.019
963
BRN014 Bronchopneumonia 45 0.019
964
c PST005 Posterior Uveitis 45 0.019
965
P ACT150 Acute Adrenal Insufficiency 45 0.019
966
AYM001 Ayme-Gripp Syndrome 45 0.019
967
CNG048 Congenital Hepatic Fibrosis 45 0.019
968
ACN018 Acne Inversa, Familial, 1 45 0.019
969
BBS001 Babesiosis 45 0.019
970
SKN027 Skin Conditions 45 0.019
971
P MGS004 Meige Syndrome 45 0.019
972
P ATR005 Atrophic Gastritis 45 0.019
973
END020 Endocardial Fibroelastosis 44 0.019
974
CRR007 Cirrhosis, Cryptogenic 44 0.019
975
c MTR002 Mitral Valve Insufficiency 44 0.019
976
P SDR002 Siderosis 44 0.019
977
c ADN012 Adenocarcinoma in Situ 44 0.019
978
BHR001 Behr Syndrome 44 0.019
979
RTN001 Retinal Vasculitis 44 0.019
980
ANX004 Anoxia 44 0.019
981
ENC044 Enchondromatosis, Multiple, Ollier Type 44 0.019
982
c LNG031 Lung Benign Neoplasm 44 0.019
983
LFT009 Left Ventricular Outflow Tract Obstruction 44 0.019
984
PLS029 Plasminogen Activator Inhibitor-1 Deficiency 44 0.019
985
TBR006 Tuberculoid Leprosy 44 0.019
986
PLR005 Pleuropneumonia 43 0.019
987
ERY029 Erythermalgia, Primary 43 0.019
988
DRM013 Dermoid Cyst 43 0.019
989
CRB008 Cerebral Atherosclerosis 43 0.019
990
P PSD003 Pseudohypoaldosteronism 43 0.019
991
NLS001 Nelson Syndrome 43 0.019
992
P PMP005 Pemphigus Vulgaris 43 0.019
993
PRM236 Primary Biliary Cholangitis 43 0.019
994
END038 Endocrine Pancreas Disease 43 0.019
995
PLC001 Placenta Accreta 43 0.019
996
GST009 Gastroschisis 43 0.019
997
EPS023 Epstein-Barr Virus-Associated Gastric Carcinoma 43 0.019
998
SPN032 Spindle Cell Carcinoma 43 0.019
999
FRS002 Frasier Syndrome 42 0.019
1000
LYM006 Lymphoepithelioma-Like Carcinoma 42 0.019
1001
LMY002 Leiomyoma 42 0.019
1002
P CRB088 Cerebral Atrophy 42 0.019
1003
TRP008 Tropical Calcific Pancreatitis 42 0.019
1004
CTN004 Cutaneous Fibrous Histiocytoma 42 0.019
1005
NPH010 Nephrosclerosis 42 0.019
1006
c CLR085 Colorectal Cancer 1 42 0.019
1007
FBR003 Fibrous Histiocytoma 42 0.019
1008
PRT026 Parotitis 42 0.019
1009
TBL003 Tubular Adenocarcinoma 42 0.019
1010
IMM127 Immune System Cancer 42 0.019
1011
BRN118 Brain Small Vessel Disease with or Without Ocular Anomalies 42 0.019
1012
KLT001 Klatskin's Tumor 42 0.019
1013
CMP010 Complex Regional Pain Syndrome 42 0.019
1014
FCT005 Factor Xiii Deficiency 42 0.019
1015
SYR002 Syringocystadenoma Papilliferum 42 0.019
1016
BND014 Bone Development Disease 42 0.019
1017
SPN119 Spondylarthropathy 41 0.019
1018
P CNG390 Congenital Pulmonary Airway Malformation 41 0.019
1019
BRN015 Bronchiolo-Alveolar Adenocarcinoma 41 0.019
1020
CYS036 Cystinosis, Nephropathic 41 0.019
1021
BRS064 Bursitis 41 0.019
1022
PRP028 Peripheral Vertigo 41 0.019
1023
INT071 Intestinal Perforation 41 0.019
1024
TBR008 Tuberculous Peritonitis 41 0.019
1025
SPN369 Spinal Disease 41 0.019
1026
SRC002 Sarcomatoid Renal Cell Carcinoma 41 0.019
1027
c ADL001 Adult Lymphoma 41 0.019
1028
P BNG032 Benign Mesothelioma 41 0.019
1029
c RCR022 Recurrent Acute Pancreatitis 41 0.019
1030
P ACQ009 Acquired Metabolic Disease 41 0.019
1031
CRT008 Carotid Artery Dissection 41 0.019
1032
P FML187 Familial Hypertension 41 0.019
1033
MYS001 Myositis Ossificans 41 0.019
1034
P CYS017 Cystic Teratoma 41 0.019
1035
CRV068 Cervical Polyp 41 0.019
1036
HMT018 Hematopoietic Stem Cell Transplantation 41 0.019
1037
CHR034 Chromophobe Adenoma 41 0.019
1038
c GST048 Gastrointestinal System Benign Neoplasm 41 0.019
1039
c HRD012 Hereditary Elliptocytosis 41 0.019
1040
SCR001 Secretory Meningioma 41 0.019
1041
INT060 Intestinal Atresia 40 0.019
1042
STR079 Sturge-Weber Syndrome, Somatic, Mosaic 40 0.019
1043
MYF002 Myofascial Pain Syndrome 40 0.019
1044
TST043 Testicular Seminoma 40 0.019
1045
c JVN003 Juvenile Xanthogranuloma 40 0.019
1046
CLC001 Calciphylaxis 40 0.019
1047
ISC015 Ischemic Colitis 40 0.019
1048
MLN013 Melanoma Metastasis 40 0.019
1049
CRN031 Cranial Nerve Disease 40 0.019
1050
MLT145 Multiple Enchondromatosis, Maffucci Type 40 0.019
1051
MCN008 Mucinous Cystadenocarcinoma 40 0.019
1052
APP009 Appendix Adenocarcinoma 40 0.019
1053
CRN020 Coronary Restenosis 40 0.019
1054
BLD032 Bile Duct Adenocarcinoma 40 0.019
1055
c PNC106 Pancreatic Agenesis 1 40 0.019
1056
NSL003 Nasal Cavity Adenocarcinoma 40 0.019
1057
c OST112 Osteoarthritis-5 40 0.019
1058
ADN002 Adenoiditis 40 0.019
1059
DND018 Dendritic Cell Tumor 40 0.019