Search results for "thrombosis"

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

950 hits were found for 'thrombosis'

# Family MCID Name MIFTS Score
1
SGT001 Sagittal Sinus Thrombosis 40 5.902
2
PRT018 Portal Vein Thrombosis 47 5.665
3
INT078 Intracranial Thrombosis 27 5.417
4
CRN017 Coronary Thrombosis 50 5.188
5
LTR002 Lateral Sinus Thrombosis 21 4.709
6
CVR002 Cavernous Sinus Thrombosis 23 4.407
7
CRT004 Carotid Artery Thrombosis 39 4.214
8
HPT002 Hepatic Vein Thrombosis 35 4.127
9
c THR092 Thrombophilia Due to Thrombin Defect 41 3.874
10
INT076 Intracranial Sinus Thrombosis 11 3.364
11
CRB132 Cerebral Sinovenous Thrombosis 37 3.046
12
P BDD001 Budd-Chiari Syndrome 61 2.201
13
MND006 Mondor Disease 17 1.919
14
THR055 Thrombophilia, X-Linked, Due to Factor Ix Defect 12 1.919
15
HMC020 Homocystinuria, B6-Responsive and Nonresponsive Types 24 1.900
16
VNS012 Venous Thoracic Outlet Syndrome 17 1.900
17
CRB009 Cerebritis 33 0.531
18
P HPT021 Hepatitis 55 0.280
19
PRT014 Protein S Deficiency 55 0.278
20
P THR015 Thrombophilia 57 0.272
21
P MYC007 Myocardial Infarction 81 0.267
22
PLM033 Pulmonary Embolism 56 0.254
23
P THR014 Thrombocytopenia 56 0.248
24
HPR003 Heparin-Induced Thrombocytopenia 46 0.242
25
PRT011 Protein C Deficiency 54 0.236
26
P ANT006 Antiphospholipid Syndrome 55 0.232
27
ANR040 Aneurysm 35 0.207
28
HPT023 Hepatocellular Carcinoma 95 0.199
29
c SYS001 Systemic Lupus Erythematosus 91 0.187
30
P LPS004 Lupus Erythematosus 67 0.185
31
P ESS003 Essential Thrombocythemia 66 0.176
32
HYP037 Hyperhomocysteinemia 45 0.176
33
END072 Endotheliitis 44 0.173
34
P NPH012 Nephrotic Syndrome 60 0.164
35
P LKM002 Leukemia 66 0.149
36
c ACT075 Acute Myocardial Infarction 57 0.147
37
PLY001 Polycythemia Vera 75 0.145
38
P PNC044 Pancreatitis 59 0.145
39
P PLY018 Polycythemia 58 0.143
40
CLT003 Colitis 54 0.142
41
THR016 Thrombophlebitis 58 0.140
42
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 51 0.138
43
HMG002 Hemoglobinuria 43 0.138
44
ULC004 Ulcerative Colitis 63 0.134
45
HDC001 Headache 50 0.132
46
P PRT013 Portal Hypertension 49 0.132
47
LVR012 Liver Cirrhosis 66 0.130
48
ART111 Artery Disease 55 0.130
49
P SNS014 Sinusitis 56 0.126
50
ATH003 Atherosclerosis 56 0.124
51
P MNN013 Meningitis 58 0.117
52
THR004 Thrombocytosis 50 0.117
53
DSS009 Disseminated Intravascular Coagulation 52 0.115
54
RTN023 Retinitis 44 0.115
55
PRP030 Purpura 54 0.113
56
PST095 Post-Thrombotic Syndrome 36 0.113
57
INT003 Intracranial Hypotension 23 0.113
58
OTT002 Otitis Media 56 0.110
59
P INF037 Inflammatory Bowel Disease 39 0.110
60
P HYP098 Hypereosinophilic Syndrome 55 0.108
61
CLL003 Cellulitis 50 0.108
62
HDN002 Head Injury 41 0.108
63
ISC004 Ischemia 53 0.103
64
P DYS026 Dysfibrinogenemia 52 0.103
65
P ART084 Arteriovenous Fistula 40 0.103
66
P CRN211 Coronary Artery Disease 73 0.100
67
OVR029 Ovarian Hyperstimulation Syndrome 60 0.100
68
P HMC002 Homocystinuria 52 0.100
69
INT075 Intracranial Hypertension 43 0.097
70
PSD002 Pseudotumor Cerebri 47 0.095
71
TBR010 Tuberculosis 73 0.092
72
FCT004 Factor Xii Deficiency 58 0.092
73
P BLN003 Blindness 47 0.092
74
THR013 Thoracic Outlet Syndrome 45 0.092
75
CRN006 Coronary Aneurysm 40 0.086
76
P OBS005 Obesity 94 0.083
77
c ACT027 Acute Pancreatitis 55 0.083
78
P ADN016 Adenocarcinoma 49 0.083
79
MYM001 Myoma 46 0.083
80
CRD137 Cardiogenic Shock 42 0.083
81
P MYL005 Myelofibrosis 68 0.080
82
BHC002 Behcet's Disease 68 0.080
83
P HMP007 Hemophilia 59 0.080
84
DFC004 Deficiency Anemia 54 0.080
85
SPR035 Superior Vena Cava Syndrome 34 0.080
86
SPL006 Splenic Infarction 32 0.080
87
LMR001 Lemierre's Syndrome 28 0.080
88
ORB006 Orbital Cellulitis 25 0.080
89
P PLM037 Pulmonary Hypertension 85 0.076
90
P RNL014 Renal Cell Carcinoma 83 0.076
91
FCT007 Factor Vii Deficiency 70 0.076
92
CRH001 Crohn's Disease 71 0.076
93
STR067 Stroke, Ischemic 65 0.076
94
P AFB001 Afibrinogenemia 55 0.076
95
IRN001 Iron Deficiency Anemia 48 0.076
96
P OST028 Osteochondroma 47 0.076
97
CTS005 Catastrophic Antiphospholipid Syndrome 45 0.076
98
CYT008 Cytomegalovirus Infection 39 0.076
99
THR006 Thromboangiitis Obliterans 68 0.073
100
P LVR013 Liver Disease 62 0.073
101
P GLM007 Glomerulonephritis 59 0.073
102
CRB039 Cerebrovascular Disease 59 0.073
103
VSC007 Vascular Disease 59 0.073
104
P LYM026 Lymphoblastic Leukemia 55 0.073
105
PPL021 Papilledema 46 0.073
106
MMB002 Membranous Glomerulonephritis 40 0.073
107
P ANG001 Angelman Syndrome 66 0.069
108
c HMP029 Hemophilia a 66 0.069
109
P HYD006 Hydrocephalus 56 0.069
110
ACN002 Acanthosis Nigricans 55 0.069
111
SCK005 Sickle Cell Disease 54 0.069
112
ART005 Arteriovenous Malformation 53 0.069
113
PTN001 Patent Foramen Ovale 52 0.069
114
P CRV039 Cervicitis 49 0.069
115
P RTN022 Retinal Vein Occlusion 48 0.069
116
c SPN225 Spondyloarthropathy 1 48 0.069
117
P HYP083 Hypopituitarism 47 0.069
118
VRC005 Varicose Veins 40 0.069
119
P TRC086 Trichohepatoenteric Syndrome 1 39 0.069
120
CRT015 Carotid Artery Occlusion 37 0.069
121
c ART101 Aortic Valve Disease 2 32 0.069
122
P ATX010 Ataxia Neuropathy Spectrum 29 0.069
123
P BRS047 Breast Cancer 90 0.065
124
VNW001 Von Willebrand's Disease 67 0.065
125
KWS002 Kawasaki Disease 66 0.065
126
P THL005 Thalassemia 64 0.065
127
VSC011 Vasculitis 57 0.065
128
THY033 Thyrotoxicosis 49 0.065
129
c CNT016 Central Retinal Vein Occlusion 49 0.065
130
P INT030 Intracranial Aneurysm 48 0.065
131
CHY006 Chylous Ascites 40 0.065
132
THR035 Thrombasthenia 37 0.065
133
SPN185 Spinal Cord Infarction 36 0.065
134
MYT019 May-Thurner Syndrome 22 0.065
135
SPH007 Sphenoid Sinusitis 21 0.065
136
CDS001 Cadasil 73 0.061
137
c HMP004 Hemophilia B 72 0.061
138
MYL009 Myelodysplastic Syndrome 67 0.061
139
P ART022 Arthritis 65 0.061
140
P MYL006 Myeloid Leukemia 64 0.061
141
ART016 Aortic Aneurysm 62 0.061
142
PRT036 Peritonitis 61 0.061
143
SRC014 Sarcoma 61 0.061
144
ART021 Arteriosclerosis 58 0.061
145
P HRD011 Hereditary Spherocytosis 56 0.061
146
P HYP076 Hyperthyroidism 54 0.061
147
P ESN007 Eosinophilia 54 0.061
148
ART001 Arterial Tortuosity Syndrome 48 0.061
149
P END033 Endocarditis 48 0.061
150
P RTN014 Retinal Artery Occlusion 47 0.061
151
HMR001 Hemorrhagic Thrombocythemia 46 0.061
152
HLL004 Hellp Syndrome 46 0.061
153
HMC014 Homocysteinemia 40 0.061
154
EVN001 Evans' Syndrome 39 0.061
155
ANG054 Angina Pectoris 43 0.061
156
P CRN074 Coronary Artery Aneurysm 35 0.061
157
SPP008 Suppurative Otitis Media 34 0.061
158
FCT013 Factor V Leiden Thrombophilia 31 0.061
159
P APL001 Aplastic Anemia 76 0.056
160
P ATX030 Ataxia-Telangiectasia 76 0.056
161
P PNM007 Pneumonia 64 0.056
162
ASP006 Aspergillosis 63 0.056
163
GLN010 Glanzmann Thrombasthenia 63 0.056
164
c HYP595 Hypertension, Essential 66 0.056
165
c HPT016 Hepatitis B 60 0.056
166
c PRC016 Pre-Eclampsia 58 0.056
167
FCT006 Factor V Deficiency 58 0.056
168
c HPT001 Hepatitis C 57 0.056
169
SND002 Sneddon Syndrome 54 0.056
170
P ESP024 Esophagitis 54 0.056
171
P ECL001 Eclampsia 53 0.056
172
P AND016 Andersen Syndrome 54 0.056
173
P THR005 Thrombotic Thrombocytopenic Purpura 53 0.056
174
CHL067 Cholecystitis 53 0.056
175
P NRP001 Neuropathy 52 0.056
176
SPH001 Sapho Syndrome 52 0.056
177
BLR001 Biliary Atresia 51 0.056
178
ISC002 Ischemic Optic Neuropathy 49 0.056
179
c ACT073 Acute Leukemia 48 0.056
180
HPT019 Hepatic Encephalopathy 51 0.056
181
BCT015 Bacteremia 45 0.056
182
ISC015 Ischemic Colitis 45 0.056
183
BRN106 Burns 42 0.056
184
NNT024 Neonatal Stroke 40 0.056
185
MDS022 Mediastinitis 39 0.056
186
P VNS003 Venous Insufficiency 39 0.056
187
BRS090 Breast Reconstruction 38 0.056
188
BRN026 Branch Retinal Artery Occlusion 36 0.056
189
PTR001 Petrositis 24 0.056
190
HGH021 Hughes-Stovin Syndrome 20 0.056
191
c THR023 Thrombophilia Due to Thrombomodulin Defect 11 0.056
192
P PHC003 Pheochromocytoma 79 0.051
193
P DBT085 Diabetes Mellitus, Insulin-Dependent 83 0.051
194
P LPR003 Leprosy 71 0.051
195
SCK003 Sickle Cell Anemia 70 0.051
196
RLP001 Relapsing Polychondritis 63 0.051
197
P CNG401 Congenital Heart Disease 62 0.051
198
P TMP003 Temporal Arteritis 62 0.051
199
P ATR011 Atrial Fibrillation 62 0.051
200
FCT003 Factor X Deficiency 58 0.051
201
P ABD003 Abdominal Aortic Aneurysm 58 0.051
202
LGG001 Legg-Calve-Perthes Disease 58 0.051
203
SPN186 Spinal Cord Injury 54 0.051
204
P ACR001 Aicardi-Goutieres Syndrome 54 0.051
205
DBT001 Diabetic Ketoacidosis 52 0.051
206
PRP007 Priapism 51 0.051
207
OST017 Osteomyelitis 50 0.051
208
HYP063 Hypersplenism 50 0.051
209
ANR004 Anuria 48 0.051
210
DDN006 Duodenitis 48 0.051
211
P CMP008 Compartment Syndrome 47 0.051
212
PRT019 Protein-Losing Enteropathy 47 0.051
213
P MNT147 Mental Retardation 46 0.051
214
NPH051 Nephritis 46 0.051
215
c ACQ014 Acquired Hemophilia 45 0.051
216
CHL069 Cholesteatoma 45 0.051
217
c CNT028 Central Retinal Artery Occlusion 45 0.051
218
FCT005 Factor Xiii Deficiency 44 0.051
219
MLK003 Melkersson-Rosenthal Syndrome 44 0.051
220
P PYL005 Pyelonephritis 43 0.051
221
c ACQ012 Acquired Angioedema 43 0.051
222
ERY004 Erysipelas 42 0.051
223
MNN021 Meningococcemia 41 0.051
224
ABD004 Abdominal Tuberculosis 39 0.051
225
RTR011 Retroperitoneal Fibrosis 39 0.051
226
ZYG002 Zygomycosis 39 0.051
227
VND001 Vein Disease 38 0.051
228
THR104 Thrombophilia Due to Antithrombin Iii Deficiency 38 0.051
229
CHR466 Chronic Thromboembolic Pulmonary Hypertension 35 0.051
230
LCK001 Locked-in Syndrome 35 0.051
231
PRP028 Peripheral Vertigo 34 0.051
232
BLD054 Blood Protein Disease 31 0.051
233
c FRN011 Frontal Sinusitis 25 0.051
234
SBD001 Subdural Empyema 23 0.051
235
HRD083 Hereditary Antithrombin Deficiency 20 0.051
236
c BNG076 Benign Exophthalmos Syndrome 19 0.051
237
ORB016 Orbital Varix 12 0.051
238
P LNG032 Lung Cancer 94 0.046
239
AND015 Androgen Insensitivity 69 0.046
240
TTR001 Tetralogy of Fallot 67 0.046
241
BRK010 Burkitt Lymphoma 63 0.046
242
SCH014 Schistosomiasis 60 0.046
243
P HML002 Hemolytic Anemia 56 0.046
244
P MYL007 Myeloma 53 0.046
245
TYP007 Typhoid Fever 53 0.046
246
P LMY004 Leiomyosarcoma 53 0.046
247
P INT070 Intestinal Obstruction 53 0.046
248
P HMR012 Hemorrhagic Fever 52 0.046
249
P END047 Endophthalmitis 51 0.046
250
NDL013 Nodular Regenerative Hyperplasia 51 0.046
251
PRS047 Prostatitis 51 0.046
252
FCT001 Factor Viii Deficiency 51 0.046
253
PRT093 Proteus Syndrome, Somatic 50 0.046
254
ADR015 Adrenocortical Carcinoma 49 0.046
255
P AXN010 Axenfeld-Rieger Syndrome, Type 3 50 0.046
256
CHR001 Churg-Strauss Syndrome 49 0.046
257
MRB003 Morbid Obesity 52 0.046
258
APP008 Appendicitis 48 0.046
259
KLN001 Klinefelter's Syndrome 47 0.046
260
URM002 Uremia 47 0.046
261
RDC002 Radiculopathy 47 0.046
262
CRD001 Cardiac Tamponade 46 0.046
263
MYL001 Myelitis 46 0.046
264
ACQ007 Acquired Immunodeficiency Syndrome 46 0.046
265
PRC013 Pericarditis 45 0.046
266
c SVR056 Severe Hemophilia a 43 0.046
267
EXS001 Exostosis 43 0.046
268
OPT009 Optic Neuritis 42 0.046
269
CCN002 Cocaine Abuse 42 0.046
270
VRC001 Varicocele 42 0.046
271
NRT004 Neuritis 40 0.046
272
CHL004 Cholelithiasis 40 0.046
273
ACT055 Actinomycosis 40 0.046
274
FSC004 Fasciitis 39 0.046
275
CRT012 Cortical Blindness 36 0.046
276
NRN002 Neuronitis 36 0.046
277
NPH017 Nephrosis 36 0.046
278
CDQ001 Cauda Equina Syndrome 35 0.046
279
CRB086 Cerebral Aneurysms 33 0.046
280
SCR015 Scarlet Fever 31 0.046
281
PRP080 Peripheral Artery Disease 30 0.046
282
INF133 Inferior Vena Cava Interruption 30 0.046
283
HMC016 Homocystinuria Due to Cbs Deficiency 29 0.046
284
VNF001 Vein of Galen Aneurysm 27 0.046
285
MTH044 Mthfr Gene Mutation 25 0.046
286
SHW001 Shwartzman Phenomenon 20 0.046
287
HMC030 Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency 17 0.046
288
THN005 Thunderclap Headache 16 0.046
289
P ACT061 Acute Sphenoidal Sinusitis 14 0.046
290
THR088 Thrombophilia Due to Protein S Deficiency, Autosomal Recessive 11 0.046
291
c MLT019 Multiple Myeloma 75 0.040
292
P TRN020 Turner Syndrome 58 0.040
293
GSG001 Gas Gangrene 58 0.040
294
c ATM010 Autoimmune Hemolytic Anemia 57 0.040
295
P KDN018 Kidney Disease 57 0.040
296
PHR003 Pharyngitis 56 0.040
297
P THY032 Thyroiditis 56 0.040
298
P ENC004 Encephalitis 56 0.040
299
P SZR006 Seizure Disorder 56 0.040
300
GST009 Gastroschisis 55 0.040
301
MLN008 Melanoma 55 0.040
302
GRV001 Graves' Disease 54 0.040
303
c VRL010 Viral Hepatitis 54 0.040
304
P PSR002 Psoriasis 54 0.040
305
c MLG069 Malignant Hypertension 54 0.040
306
CRN036 Craniopharyngioma 54 0.040
307
HYD012 Hydrops Fetalis 53 0.040
308
P CNJ013 Conjunctivitis 53 0.040
309
HYP066 Hyperglycemia 52 0.040
310
P MTR012 Mitral Valve Disease 52 0.040
311
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 53 0.040
312
P RNV001 Renovascular Hypertension 52 0.040
313
c HPT073 Hepatitis C Virus 51 0.040
314
P MYM002 Moyamoya Disease 51 0.040
315
CHC001 Chickenpox 51 0.040
316
CHR074 Choriocarcinoma 50 0.040
317
LYM019 Lymphosarcoma 50 0.040
318
P MST018 Mesothelioma 51 0.040
319
P SLP006 Sleep Apnea 50 0.040
320
c ACT134 Acute Liver Failure 48 0.040
321
ANG011 Angiodysplasia 48 0.040
322
INT002 Intermittent Claudication 47 0.040
323
P EXP004 Exophthalmos 47 0.040
324
PNM013 Pneumococcal Meningitis 47 0.040
325
OCL006 Ocular Hypertension 47 0.040
326
P BCL006 B-Cell Lymphomas 47 0.040
327
c PND001 Pain Disorder 46 0.040
328
INT221 Intravascular Large B-Cell Lymphoma 46 0.040
329
HST009 Histiocytoma 46 0.040
330
EBS001 Ebstein Anomaly 46 0.040
331
SPT004 Septic Arthritis 45 0.040
332
P LYM025 Lymphedema 45 0.040
333
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 45 0.040
334
CRB153 Cerebral Arteriovenous Malformation 46 0.040
335
HNC001 Henoch-Schoenlein Purpura 44 0.040
336
LPS007 Lupus Nephritis 44 0.040
337
ANG018 Angiomyolipoma 43 0.040
338
LPD004 Lipoid Nephrosis 43 0.040
339
HMR002 Hemarthrosis 43 0.040
340
END021 Endomyocardial Fibrosis 42 0.040
341
SPN035 Spindle Cell Sarcoma 41 0.040
342
P PNC001 Pancytopenia 41 0.040
343
ACQ017 Acquired Von Willebrand Syndrome 41 0.040
344
PRP016 Paraplegia 40 0.040
345
ESN011 Eisenmenger Syndrome 40 0.040
346
VTM002 Vitamin B12 Deficiency 40 0.040
347
LYM021 Lymphadenitis 39 0.040
348
VNW005 Von Willebrand Disease, Type 1 39 0.040
349
MYH001 May-Hegglin Anomaly 39 0.040
350
ART110 Arteritic Anterior Ischemic Optic Neuropathy 38 0.040
351
LMB062 Limb Ischemia 38 0.040
352
CRP018 Cor Pulmonale 37 0.040
353
c INF069 Infantile Neuroaxonal Dystrophy 1 36 0.040
354
c ACT042 Acute Pyelonephritis 36 0.040
355
EPD005 Epidural Abscess 35 0.040
356
AMR003 Amaurosis Fugax 35 0.040
357
CRB085 Cerebral Hemorrhage 35 0.040
358
INF013 Inferior Myocardial Infarction 33 0.040
359
BCK006 Back Pain 33 0.040
360
c CHR431 Chronic Venous Insufficiency 32 0.040
361
STR044 Steroid-Resistant Nephrotic Syndrome 31 0.040
362
PSL001 Pasli Disease 30 0.040
363
P LBY004 Labyrinthitis 29 0.040
364
UND005 Undifferentiated Pleomorphic Sarcoma 28 0.040
365
PRT045 Prothrombin-Related Thrombophilia 26 0.040
366
BSL004 Basilar Artery Occlusion 23 0.040
367
IRN002 Iron Metabolism Disease 22 0.040
368
THR067 Thrombophilia Due to Protein C Deficiency, Autosomal Dominant 17 0.040
369
ABD009 Abducens Palsy 18 0.040
370
THR089 Thrombophilia Due to Protein S Deficiency, Autosomal Dominant 16 0.040
371
DBL009 Double Inferior Vena Cava 16 0.040
372
CNG058 Congenital Antithrombin Deficiency Type 3 14 0.040
373
c ANT041 Antiphospholipid Syndrome, Familial 13 0.040
374
HRD147 Hereditary Thrombophilia Due to Congenital Protein S Deficiency 12 0.040
375
NNT044 Neonatal Antiphospholipid Syndrome 12 0.040
376
PRN017 Perianal Hematoma 11 0.040
377
CYS001 Cystic Fibrosis 92 0.032
378
P CLR023 Colorectal Cancer 96 0.032
379
P RHM011 Rheumatoid Arthritis 94 0.032
380
P PNC035 Pancreatic Cancer 82 0.032
381
P CSH001 Cushing's Syndrome 76 0.032
382
HV1006 Hiv-1 83 0.032
383
P CHR090 Chronic Lymphocytic Leukemia 74 0.032
384
P MDL005 Medulloblastoma 71 0.032
385
P CLC005 Celiac Disease 69 0.032
386
OBS002 Obsessive-Compulsive Disorder 69 0.032
387
P TBR001 Tuberous Sclerosis 68 0.032
388
MGR002 Migraine 64 0.032
389
P AST007 Astrocytoma 63 0.032
390
MLG056 Malignant Hyperthermia 62 0.032
391
ANR007 Anorexia Nervosa 62 0.032
392
P MST009 Mastocytosis 61 0.032
393
TKY001 Takayasu's Arteritis 60 0.032
394
P HMN010 Hemangioma 60 0.032
395
P DYS007 Dyskeratosis Congenita 60 0.032
396
PLY017 Polyarteritis Nodosa 60 0.032
397
c SYS004 Systemic Mastocytosis 60 0.032
398
P HYP086 Hypothyroidism 59 0.032
399
CHL065 Cholangiocarcinoma 59 0.032
400
P PRD008 Periodontitis 59 0.032
401
PRP027 Peripheral Vascular Disease 60 0.032
402
P END044 Endometriosis 59 0.032
403
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 58 0.032
404
DRM006 Dermatitis 58 0.032
405
c LKM062 Leukemia, Acute Lymphoblastic 58 0.032
406
DBN001 Dubin-Johnson Syndrome 57 0.032
407
c ALM001 Al Amyloidosis 56 0.032
408
P LPS002 Liposarcoma 56 0.032
409
PMS001 Poems Syndrome 56 0.032
410
P EHL001 Ehlers-Danlos Syndrome 56 0.032
411
ADN018 Adenoma 55 0.032
412
P SCH018 Schizencephaly 55 0.032
413
CRB037 Cerebral Palsy 55 0.032
414
ATP002 Atopy 55 0.032
415
CYS005 Cysticercosis 54 0.032
416
P MSC005 Muscular Dystrophy 54 0.032
417
ADL030 Adult-Onset Still's Disease 54 0.032
418
P ANP001 Anaplastic Large Cell Lymphoma 53 0.032
419
P RBL001 Rubella 53 0.032
420
HYP056 Hypoglycemia 53 0.032
421
P PLY014 Polycystic Kidney Disease 53 0.032
422
HPT022 Hepatoblastoma 53 0.032
423
c PNC108 Pancreatitis, Hereditary 54 0.032
424
P MYP004 Myopathy 53 0.032
425
P DBT005 Diabetes Insipidus 53 0.032
426
c LKM063 Leukemia, Chronic Myeloid 53 0.032
427
ART031 Aortic Coarctation 52 0.032
428
GNG013 Gingivitis 52 0.032
429
ASP003 Aseptic Meningitis 52 0.032
430
MYC002 Mycobacterium Avium Complex Disease 51 0.032
431
P FML161 Familial Mediterranean Fever, Ar 51 0.032
432
P HYP080 Hypogonadism 51 0.032
433
TXC005 Toxic Shock Syndrome 51 0.032
434
DWN001 Down Syndrome 51 0.032
435
PLY041 Polymyositis 51 0.032
436
VGN023 Vaginitis 51 0.032
437
P CTR002 Cataract 50 0.032
438
CNN005 Connective Tissue Disease 50 0.032
439
c HPT015 Hepatitis D 50 0.032
440
CVR006 Cavernous Hemangioma 50 0.032
441
P MYC008 Myocarditis 50 0.032
442
c MLG002 Malignant Peritoneal Mesothelioma 50 0.032
443
PLS011 Plasmacytoma 49 0.032
444
P SYR001 Syringomyelia 49 0.032
445
RHB003 Rhabdomyosarcoma 49 0.032
446
BRN071 Brain Injury 49 0.032
447
HYP266 Hypoxia 49 0.032
448
PRC012 Pericardial Effusion 49 0.032
449
BRN029 Brain Disease 49 0.032
450
P ENC008 Encephalocele 49 0.032
451
LYM040 Lymphoblastic Lymphoma 49 0.032
452
CRY004 Cryoglobulinemia 49 0.032
453
MCR088 Microscopic Polyangiitis 49 0.032
454
TNS005 Tonsillitis 48 0.032
455
PYD001 Pyoderma Gangrenosum 48 0.032
456
ACT017 Acute Chest Syndrome 48 0.032
457
P PRN026 Porencephaly 48 0.032
458
INT007 Intermediate Coronary Syndrome 47 0.032
459
P OPH004 Ophthalmoplegia 47 0.032
460
ORL011 Oral Cancer 47 0.032
461
TRM010 Traumatic Brain Injury 46 0.032
462
PRN011 Pernicious Anemia 46 0.032
463
STS002 Situs Inversus 46 0.032
464
END031 Endometrial Stromal Sarcoma 46 0.032
465
BRN004 Brain Edema 46 0.032
466
LPT001 Leptospirosis 46 0.032
467
P CHL066 Cholangitis 45 0.032
468
P HYD002 Hydronephrosis 45 0.032
469
MCN001 Mucinous Adenocarcinoma 45 0.032
470
CRV031 Cervical Adenocarcinoma 44 0.032
471
HMP005 Hemiplegia 44 0.032
472
DGS001 Degos Disease 44 0.032
473
P NNT009 Neonatal Diabetes Mellitus 44 0.032
474
PRT039 Proteinuria 43 0.032
475
PYD002 Pyoderma 43 0.032
476
PLV003 Pelvic Inflammatory Disease 43 0.032
477
BNM001 Bone Marrow Cancer 43 0.032
478
c CHR092 Chronic Myeloproliferative Disease 43 0.032
479
VSC044 Visceral Myopathy 43 0.032
480
CRN014 Cronkhite-Canada Syndrome 43 0.032
481
BLD034 Bile Duct Carcinoma 43 0.032
482
MNN014 Mononeuritis 43 0.032
483
CRN020 Coronary Restenosis 42 0.032
484
OBS001 Obstructive Jaundice 42 0.032
485
P APL006 Aplasia Cutis Congenita 42 0.032
486
c BCT007 Bacterial Meningitis 42 0.032
487
KLP010 Klippel-Trenaunay-Weber Syndrome 43 0.032
488
SMN007 Seminoma 42 0.032
489
TRN007 Transsexualism 42 0.032
490
P HMR005 Hemorrhoid 41 0.032
491
SPL004 Splenic Marginal Zone Lymphoma 40 0.032
492
SPL018 Splenomegaly 40 0.032
493
CNS002 Constrictive Pericarditis 40 0.032
494
RTN021 Retinal Vascular Occlusion 39 0.032
495
URT010 Ureteral Obstruction 39 0.032
496
HPT008 Hepatic Tuberculosis 39 0.032
497
HMN016 Hemangioendothelioma 39 0.032
498
TYP015 Type 2b Von Willebrand Disease 39 0.032
499
c HMG003 Hemoglobin E Disease 39 0.032
500
P OVR046 Ovarian Cyst 39 0.032
501
NCR007 Necrotizing Fasciitis 38 0.032
502
CLL002 Collecting Duct Carcinoma 37 0.032
503
TRN012 Transient Global Amnesia 37 0.032
504
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 38 0.032
505
P HRN001 Horner's Syndrome 36 0.032
506
OBS004 Obstructive Hydrocephalus 36 0.032
507
PRS045 Prostatic Hypertrophy 35 0.032
508
ESP002 Esophageal Varix 35 0.032
509
MCR225 Macrophage Activation Syndrome 35 0.032
510
BLR015 Blue Rubber Bleb Nevus Syndrome 35 0.032
511
THR100 Thrombocytopenic Purpura, Autoimmune 35 0.032
512
FCL012 Facial Paralysis 35 0.032
513
INT079 Intrahepatic Cholangiocarcinoma 34 0.032
514
UTR039 Uterine Fibroid 34 0.032
515
P PRT096 Peritoneal Mesothelioma 32 0.032
516
IPX001 Ipex Syndrome 32 0.032
517
VRL011 Viral Infectious Disease 31 0.032
518
HNS001 Hansen's Disease 31 0.032
519
RHM028 Rheumatic Heart Disease 32 0.032
520
MYS004 Myiasis 31 0.032
521
CGN006 Cogan Syndrome 31 0.032
522
c SYS043 Systemic Lupus Erythematosus 1 30 0.032
523
NRS005 Neurosarcoidosis 30 0.032
524
c SBC003 Subacute Bacterial Endocarditis 29 0.032
525
LYM014 Lymphangitis 28 0.032
526
LYM005 Lymphocele 27 0.032
527
c THR082 Thrombophilia Due to Activated Protein C Resistance 27 0.032
528
P ATM020 Autoimmune Enteropathy 26 0.032
529
P CRN035 Cranial Nerve Palsy 26 0.032
530
FBR028 Fibrosing Mediastinitis 25 0.032
531
WND002 Wandering Spleen 24 0.032
532
LNG095 Lung Abscess 25 0.032
533
ALX001 Alexia 24 0.032
534
PRR008 Periarteritis Nodosa 23 0.032
535
PRX023 Paroxysmal Nocturnal Hemoglobinuria, Somatic 22 0.032
536
PRM008 Parametritis 22 0.032
537
MMB005 Membranous Glomerulonephritis, Antenatal 21 0.032
538
ETH009 Ethmoid Sinusitis 21 0.032
539
STR077 Streptococcal Toxic-Shock Syndrome 22 0.032
540
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 20 0.032
541
HYP319 Hypereosinophilic Syndrome, Idiopathic, Resistant to Imatinib 20 0.032
542
c ACT036 Acute Cholangitis 19 0.032
543
P SCK034 Sickle Beta Thalassemia 20 0.032
544
c ACT035 Acute Frontal Sinusitis 17 0.032
545
THR007 Thrombophlebitis Migrans 18 0.032
546
AND005 Androgen Insensitivity Syndrome, Mild 17 0.032
547
P ERY048 Erythrocytosis, Familial, 2 17 0.032
548
CRD023 Cardiomyopathy Cataract Hip Spine Disease 17 0.032
549
MNN005 Meningovascular Neurosyphilis 16 0.032
550
BLR009 Biliary Atresia Extrahepatic 13 0.032
551
OCL024 Ocular Neuromyotonia 13 0.032
552
SNG003 Single Ventricular Heart 12 0.032
553
CRT056 Carotidynia 12 0.032
554
CNG056 Congenital Antithrombin Deficiency 11 0.032
555
ACT174 Acute Peripheral Arterial Occlusion 8 0.032
556
P ALZ034 Alzheimer Disease 100 0.023
557
P LFR001 Li-Fraumeni Syndrome 81 0.023
558
HDG012 Hodgkin Lymphoma 79 0.023
559
P OST005 Osteogenesis Imperfecta 77 0.023
560
P DLT002 Dilated Cardiomyopathy 77 0.023
561
P HYP607 Hypercholesterolemia, Familial 81 0.023
562
FBR012 Fabry Disease 76 0.023
563
P HRD008 Hereditary Hemorrhagic Telangiectasia 75 0.023
564
MLR004 Malaria 81 0.023
565
GLC006 Galactosemia 75 0.023
566
P HMC003 Hemochromatosis 75 0.023
567
ADN021 Adenomatous Polyposis Coli 75 0.023
568
DCH001 Duchenne Muscular Dystrophy 78 0.023
569
P SCL016 Scleroderma 76 0.023
570
P NRF002 Neurofibromatosis 69 0.023
571
P WSK001 Wiskott-Aldrich Syndrome 69 0.023
572
CNG034 Congestive Heart Failure 69 0.023
573
LSC001 Lesch-Nyhan Syndrome 69 0.023
574
P PRM002 Primary Hyperoxaluria 68 0.023
575
c LKM061 Leukemia, Acute Myeloid 69 0.023
576
PTZ001 Peutz-Jeghers Syndrome 68 0.023
577
P NRB001 Neuroblastoma 68 0.023
578
SVR004 Severe Combined Immunodeficiency 68 0.023
579
P DMN001 Diamond-Blackfan Anemia 66 0.023
580
P LYM007 Lymphangioleiomyomatosis 65 0.023
581
ADD001 Addison's Disease 65 0.023
582
c NRF018 Neurofibromatosis, Type 1 65 0.023
583
GLL008 Gilles De La Tourette Syndrome 64 0.023
584
P PRD006 Prader-Willi Syndrome 64 0.023
585
ORN006 Ornithine Transcarbamylase Deficiency 64 0.023
586
P AMY004 Amyloidosis 63 0.023
587
CCC001 Coccidioidomycosis 63 0.023
588
P MYS005 Myositis 63 0.023
589
P DRM010 Dermatomyositis 62 0.023
590
P HRM001 Hermansky-Pudlak Syndrome 60 0.023
591
ALC007 Alcohol Dependence 60 0.023
592
P PLY011 Polycystic Ovary Syndrome 59 0.023
593
SCR008 Scrub Typhus 59 0.023
594
P HYP061 Hypertrophic Cardiomyopathy 59 0.023
595
ARG002 Argininosuccinic Aciduria 59 0.023
596
LMY002 Leiomyoma 59 0.023
597
P GLB002 Glioblastoma 59 0.023
598
P INF038 Influenza 67 0.023
599
CRY005 Cryptococcosis 58 0.023
600
ERD001 Erdheim-Chester Disease 58 0.023
601
c ATM003 Autoimmune Thyroiditis 58 0.023
602
P SPN046 Spinal Muscular Atrophy 57 0.023
603
ACT049 Acute Disseminated Encephalomyelitis 57 0.023
604
P PRP029 Porphyria 57 0.023
605
P UVT001 Uveitis 57 0.023
606
ANN002 Anencephaly 57 0.023
607
P GST044 Gastritis 56 0.023
608
P ERY008 Erythromelalgia 56 0.023
609
P ATP001 Atopic Dermatitis 56 0.023
610
GLC085 Glucose-6-Phosphate Dehydrogenase Deficiency 57 0.023
611
WGN006 Wegener Granulomatosis 57 0.023
612
STT001 Status Epilepticus 56 0.023
613
CHL014 Cholera 56 0.023
614
P CHN012 Chondrosarcoma 56 0.023
615
DNG003 Dengue Disease 64 0.023
616
MXD005 Mixed Connective Tissue Disease 56 0.023
617
P OLG002 Oligodendroglioma 55 0.023
618
CCT002 Cicatricial Pemphigoid 55 0.023
619
BLL003 Bell's Palsy 54 0.023
620
P CRB042 Cerebellar Ataxia 54 0.023
621
BBS001 Babesiosis 54 0.023
622
CMP002 Campylobacteriosis 54 0.023
623
P ART023 Arthropathy 54 0.023
624
MYL020 Myelomeningocele 54 0.023
625
BCK001 Becker Muscular Dystrophy 61 0.023
626
JCB001 Jacobsen Syndrome 53 0.023
627
MLD001 Melioidosis 62 0.023
628
P HYP620 Hypoprothrombinemia 54 0.023
629
OLL001 Ollier Disease 53 0.023
630
GTR002 Goiter 53 0.023
631
P CMP010 Complex Regional Pain Syndrome 53 0.023
632
BRC012 Brucellosis 53 0.023
633
BRK001 Brooke-Spiegler Syndrome 52 0.023
634
c OST135 Osteogenesis Imperfecta, Type I 53 0.023
635
PLM001 Pulmonary Tuberculosis 60 0.023
636
c ACT210 Acute Respiratory Distress Syndrome 52 0.023
637
ISC006 Ischemic Heart Disease 51 0.023
638
TST021 Testicular Germ Cell Tumor 51 0.023
639
SRS001 Serous Cystadenocarcinoma 51 0.023
640
P ANG015 Angioedema 51 0.023
641
CNG048 Congenital Hepatic Fibrosis 51 0.023
642
P HMN013 Hemangiopericytoma 51 0.023
643
SPN020 Spondylosis 51 0.023
644
ECH003 Echinococcosis 51 0.023
645
P BRN009 Burning Mouth Syndrome 51 0.023
646
P DBT083 Diabetes Mellitus, Permanent Neonatal 52 0.023
647
MGC001 Megacolon 51 0.023
648
GLB015 Glioblastoma Multiforme 51 0.023
649
c HPT003 Hepatitis a 51 0.023
650
MLL005 Miller-Dieker Syndrome 50 0.023
651
P THR003 Thoracic Aortic Aneurysm 50 0.023
652
P ATX004 Ataxia 50 0.023
653
NRL005 Neurilemmoma 50 0.023
654
NRN004 Neuroendocrine Tumor 50 0.023
655
P TRT010 Teratoma 50 0.023
656
NRN001 Neuroendocrine Carcinoma 50 0.023
657
EPT020 Epithelioid Hemangioendothelioma 50 0.023
658
MTY001 Mutyh-Associated Polyposis 50 0.023
659
c PST005 Posterior Uveitis 50 0.023
660
c ACT009 Acute Monocytic Leukemia 50 0.023
661
P RTN025 Retinoschisis 50 0.023
662
P PLC011 Pilocytic Astrocytoma 49 0.023
663
NTH001 Netherton Syndrome 49 0.023
664
c SCN045 Secondary Amyloidosis 50 0.023
665
P SDR002 Siderosis 49 0.023
666
EXT010 Extramedullary Plasmacytoma 49 0.023
667
HRP004 Herpes Zoster 49 0.023
668
END020 Endocardial Fibroelastosis 49 0.023
669
AMN001 Amenorrhea 49 0.023
670
ILT001 Ileitis 49 0.023
671
P MNC007 Monocytic Leukemia 49 0.023
672
BLM002 Bulimia Nervosa 49 0.023
673
P MCR010 Microcephaly 49 0.023
674
c HRD012 Hereditary Elliptocytosis 49 0.023
675
P PLY006 Polydactyly 48 0.023
676
RNL007 Renal Tubular Acidosis 48 0.023
677
MLG077 Malignant Peripheral Nerve Sheath Tumor 48 0.023
678
P SYP003 Syphilis 48 0.023
679
MCR004 Macroglobulinemia 48 0.023
680
OBS061 Obstructive Sleep Apnea 48 0.023
681
ANK001 Ankylosis 48 0.023
682
P DND001 Dandy-Walker Syndrome 48 0.023
683
DBT008 Diabetic Angiopathy 47 0.023
684
TYP011 Typhus 47 0.023
685
P VNT002 Ventricular Septal Defect 47 0.023
686
LGN002 Legionellosis 47 0.023
687
CLC001 Calciphylaxis 47 0.023
688
MCN007 Meconium Aspiration Syndrome 47 0.023
689
MTN003 Motion Sickness 47 0.023
690
JPN002 Japanese Encephalitis 46 0.023
691
ART017 Aortic Disease 46 0.023
692
P PRT029 Parathyroid Adenoma 46 0.023
693
KLT001 Klatskin's Tumor 46 0.023
694
GST037 Gastroparesis 46 0.023
695
LKM065 Leukemia, Acute Promyelocytic 47 0.023
696
CYS014 Cystadenocarcinoma 46 0.023
697
FBR003 Fibrous Histiocytoma 46 0.023
698
GRW007 Growth Hormone Deficiency 46 0.023
699
P SHR001 Short Bowel Syndrome 45 0.023
700
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 45 0.023
701
P ADM011 Adams-Oliver Syndrome 46 0.023
702
P RST002 Restrictive Cardiomyopathy 45 0.023
703
GST060 Gastric Cancer, Somatic 45 0.023
704
P EPS003 Episodic Ataxia 45 0.023
705
STN007 Stenotrophomonas Maltophilia 45 0.023
706
SCT005 Scott Syndrome 45 0.023
707
CRT002 Cartilage-Hair Hypoplasia 45 0.023
708
PNV001 Panuveitis 45 0.023
709
PPT005 Peptic Ulcer Disease 45 0.023
710
NNL002 Nonalcoholic Steatohepatitis 45 0.023
711
P MSC003 Muscular Atrophy 44 0.023
712
KMR001 Kimura Disease 44 0.023
713
IMP002 Imperforate Anus 44 0.023
714
c INT072 Intestinal Pseudo-Obstruction 44 0.023
715
INV001 Invasive Aspergillosis 44 0.023
716
P SCL018 Scoliosis 45 0.023
717
TRN015 Transient Cerebral Ischemia 44 0.023
718
P STR020 Strabismus 44 0.023
719
SFT003 Soft Tissue Sarcoma 44 0.023
720
WBR001 Weber Syndrome 44 0.023
721
PRG008 Paragonimiasis 44 0.023
722
ALC009 Alcoholic Liver Cirrhosis 43 0.023
723
LYM012 Lymphoplasmacytic Lymphoma 43 0.023
724
NPH010 Nephrosclerosis 43 0.023
725
MYC005 Myocardial Stunning 43 0.023
726
P MLG086 Malignant Hyperthermia Susceptibility 43 0.023
727
ACS001 Acoustic Neuroma 43 0.023
728
CLN015 Colon Adenocarcinoma 43 0.023
729
CYS009 Cystadenoma 43 0.023
730
MCL003 Macular Holes 43 0.023
731
CLS010 Cluster Headache 43 0.023
732
RFL001 Reflex Sympathetic Dystrophy 43 0.023
733
CRT049 Critical Limb Ischemia 43 0.023
734
PRT026 Parotitis 43 0.023
735
LPR001 Lepromatous Leprosy 42 0.023
736
CHR288 Chronic Recurrent Multifocal Osteomyelitis 42 0.023
737
LFT009 Left Ventricular Outflow Tract Obstruction 42 0.023
738
RTN001 Retinal Vasculitis 42 0.023
739
P CST002 Castleman's Disease 42 0.023
740
P PSD003 Pseudohypoaldosteronism 42 0.023
741
INF058 Inflammatory Myofibroblastic Tumor 42 0.023
742
c CRB103 Cerebral Cavernous Malformations-1 42 0.023
743
c CNT035 Central Nervous System Disease 42 0.023
744
CNV002 Conversion Disorder 42 0.023
745
P INT060 Intestinal Atresia 42 0.023
746
CNG069 Congenital Cytomegalovirus 42 0.023
747
PYM001 Pyomyositis 42 0.023
748
TRN044 Transposition of the Great Arteries 41 0.023
749
TLN003 Telangiectasis 41 0.023
750
DVR002 Diverticulitis 41 0.023
751
PNC033 Pancreas Adenocarcinoma 41 0.023
752
NNT016 Neonatal Hemochromatosis 41 0.023
753
P ACT150 Acute Adrenal Insufficiency 41 0.023
754
P TRN034 Transverse Myelitis 41 0.023
755
MFF001 Maffucci Syndrome 42 0.023
756
PLM010 Pulmonary Edema 41 0.023
757
P CRB088 Cerebral Atrophy 40 0.023
758
c SVR005 Severe Pre-Eclampsia 40 0.023
759
CRN027 Corneal Neovascularization 40 0.023
760
PLC007 Placental Abruption 40 0.023
761
BRN014 Bronchopneumonia 40 0.023
762
CRT008 Carotid Artery Dissection 40 0.023
763
SCR024 Sacrococcygeal Teratoma 40 0.023
764
PRN021 Paranasal Sinus Disease 40 0.023
765
MTS001 Mutism 40 0.023
766
MYS001 Myositis Ossificans 39 0.023
767
FTT001 Fatty Liver Disease 39 0.023
768
TBR008 Tuberculous Peritonitis 39 0.023
769
P ATR005 Atrophic Gastritis 39 0.023
770
PLM052 Pulmonary Arteriovenous Malformation 39 0.023
771
MNN017 Mononeuropathy 39 0.023
772
WLL004 Wallerian Degeneration 39 0.023
773
MNN009 Meningoencephalitis 39 0.023
774
P NRL007 Neurologic Diseases 39 0.023
775
UTR024 Uterine Carcinosarcoma 38 0.023
776
HRS011 Horseshoe Kidney 38 0.023
777
P PTS002 Ptosis 39 0.023
778
PLR007 Pleural Empyema 38 0.023
779
PNN001 Panniculitis 38 0.023
780
ILS001 Ileus 38 0.023
781
ART004 Aortic Atherosclerosis 38 0.023
782
INF034 Infective Endocarditis 38 0.023
783
LYM011 Lymphogranuloma Venereum 37 0.023
784
RTC005 Reticulosarcoma 37 0.023
785
CMR002 Coumarin Resistance 37 0.023
786
P CHR342 Chiari Malformation 37 0.023
787
SYN036 Syncope 37 0.023
788
GPS001 Gapo Syndrome 37 0.023
789
P PRC031 Preeclampsia/eclampsia 1 38 0.023
790
ADN027 Adenomyosis 37 0.023
791
PLC005 Placental Insufficiency 37 0.023
792
CHN015 Chondrodysplasia 37 0.023
793
QDR001 Quadriplegia 37 0.023
794
ILC002 Ileocolitis 37 0.023
795
MCK002 Meckel's Diverticulum 36 0.023
796
CHR010 Chorioangioma 36 0.023
797
CRB004 Cerebral Artery Occlusion 36 0.023
798
PLR005 Pleuropneumonia 36 0.023
799
HMT018 Hematopoietic Stem Cell Transplantation 36 0.023
800
P VGN017 Vaginal Cancer 35 0.023
801
STR037 Stress Cardiomyopathy 35 0.023
802
ERY045 Erythrocytosis, Somatic 35 0.023
803
APH002 Aphasia 35 0.023
804
HYP143 Hypomyelination and Congenital Cataract 35 0.023
805
CMB021 Combined Pituitary Hormone Deficiency 35 0.023
806
GLY032 Glycosylphosphatidylinositol Deficiency 35 0.023
807
GST071 Gastrointestinal Carcinoma 35 0.023
808
INT071 Intestinal Perforation 35 0.023
809
ESN020 Eosinophilic Granulomatosis with Polyangiitis 35 0.023
810
CNT060 Central Serous Chorioretinopathy 34 0.023
811
P MNN007 Meningocele 34 0.023
812
P HYP265 Hypotonia 34 0.023
813
HPT012 Hepatocellular Fibrolamellar Carcinoma 34 0.023
814
CRD016 Cardiac Rupture 34 0.023
815
XNT001 Xanthogranulomatous Pyelonephritis 34 0.023
816
GST040 Gastric Adenocarcinoma 34 0.023
817
P BRN035 Brain Stem Glioma 34 0.023
818
PTT046 Pituitary Hormone Deficiency, Combined, 2 35 0.023
819
PRT086 Partial Hydatidiform Mole 34 0.023
820
ACL001 Acalculous Cholecystitis 34 0.023
821
SPR066 Superficial Siderosis 33 0.023
822
BNM005 Bone Marrow Necrosis 33 0.023
823
TRC023 Trichinosis 33 0.023
824
WTH001 Withdrawal Disorder 33 0.023
825
DXT002 Dextrocardia with Situs Inversus 33 0.023
826
LMY003 Leiomyomatosis 33 0.023
827
FNT004 Fainting 33 0.023
828
ART012 Aortitis 33 0.023
829
c SYS007 Systemic Capillary Leak Syndrome 32 0.023
830
TBR006 Tuberculoid Leprosy 32 0.023
831
BRN055 Bronchogenic Cyst 32 0.023
832
ALC005 Alcoholic Pancreatitis 32 0.023
833
c CHR038 Chronic Maxillary Sinusitis 32 0.023
834
P IDP070 Idiopathic Scoliosis 33 0.023
835
PRS021 Prostatic Adenoma 32 0.023
836
CHL061 Childhood Leukemia 31 0.023
837
FTD001 Foot Drop 31 0.023
838
OPT006 Optic Nerve Disease 31 0.023
839
ADN002 Adenoiditis 31 0.023
840
P PLY024 Polymicrogyria 31 0.023
841
INP001 Inappropriate Adh Syndrome 31 0.023
842
SGN002 Signet Ring Cell Adenocarcinoma 31 0.023
843
VNW004 Von Willebrand Disease, Platelet-Type 31 0.023
844
MLK004 Malakoplakia 31 0.023
845
TYP017 Type 2n Von Willebrand Disease 30 0.023
846
ANG017 Angiolipoma 30 0.023
847
PRL008 Paralytic Ileus 30 0.023
848
FTL012 Fetal and Neonatal Alloimmune Thrombocytopenia 30 0.023
849
MGL023 Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome, Somatic 30 0.023
850
P MLD013 Mild Hemophilia a 30 0.023
851
ADS002 Adie Syndrome 30 0.023
852
TYP014 Type 2a Von Willebrand Disease 29 0.023
853
PRN037 Prinzmetal's Variant Angina 29 0.023
854
c ACQ010 Acquired Polycythemia 29 0.023
855
NRC019 Neurocutaneous Melanosis, Somatic 29 0.023
856
TYP016 Type 2m Von Willebrand Disease 29 0.023
857
SPR007 Superior Mesenteric Artery Syndrome 28 0.023
858
HPT066 Hepatoportal Sclerosis 28 0.023
859
PRC010 Pericardial Mesothelioma 28 0.023
860
INT042 Internuclear Ophthalmoplegia 28 0.023
861
PSD044 Pseudopolycythaemia 28 0.023
862
49X002 49,xxxxy Syndrome 28 0.023
863
TFT003 Tufting Enteropathy 26 0.023
864
ERY029 Erythermalgia, Primary 27 0.023
865
c DYS165 Dysfibrinogenemia, Congenital 27 0.023
866
CRT028 Cor Triatriatum 27 0.023
867
CNG134 Congenitally Corrected Transposition of the Great Arteries 27 0.023
868
ULN001 Ulnar Neuropathy 26 0.023
869
P ATS208 Autosomal Dominant Macrothrombocytopenia 27 0.023
870
HNM002 Hinman Syndrome 26 0.023
871
P CMM008 Communicating Hydrocephalus 25 0.023
872
ADT003 Auditory System Disease 26 0.023
873
SBC014 Subclavian Steal Syndrome 25 0.023
874
SPL007 Splenic Abscess 25 0.023
875
MLN013 Melanoma Metastasis 24 0.023
876
RHS001 Rh Isoimmunization 24 0.023
877
c CNG189 Congenital Disorder of Glycosylation, Type Ib 25 0.023
878
NRR001 Neuroretinitis 25 0.023
879
TXC001 Toxic Megacolon 24 0.023
880
SPR032 Superficial Siderosis of the Central Nervous System 23 0.023
881
CPL011 Capillary Malformations, Congenital, 1, Somatic, Mosaic 23 0.023
882
c CHR454 Chiari Malformation Type 1 24 0.023
883
c DYS040 Dyskeratosis Congenita Autosomal Recessive 23 0.023
884
P DCR004 Dacryocystitis 23 0.023
885
c MYH004 Myh9 Related Thrombocytopenia 22 0.023
886
GNT005 Giant Hemangioma 22 0.023
887
BLD052 Blood Group Incompatibility 22 0.023
888
c CNG379 Congenital Disorder of Glycosylation, Type It 22 0.023
889
MDN008 Median Arcuate Ligament Syndrome 23 0.023
890
CRN019 Coronary Artery Vasospasm 22 0.023
891
ANT013 Anterior Spinal Artery Syndrome 21 0.023
892
PNH005 Panhypopituitarism, X-Linked 22 0.023
893
CHR158 Charles Bonnet Syndrome 21 0.023
894
c CHR097 Chronic Purulent Otitis Media 21 0.023
895
ABD002 Abducens Nerve Disease 21 0.023
896
OCL041 Oculomotor Apraxia Cogan Type 21 0.023
897
CHR034 Chromophobe Adenoma 21 0.023
898
ANG022 Angel Shaped Phalangoepiphyseal Dysplasia 20 0.023
899
PRN007 Perinephritis 19 0.023
900
c PST001 Posterior Myocardial Infarction 19 0.023
901
PRF003 Piriformis Syndrome 20 0.023
902
EMB002 Embryoma 20 0.023
903
MXD035 Mixed-Type Autoimmune Hemolytic Anemia 20 0.023
904
SBS002 Substernal Goiter 19 0.023
905
MYX006 Myxoid Leiomyosarcoma 18 0.023
906
AGR018 Agraphia 19 0.023
907
ACT201 Acute Posterior Multifocal Placoid Pigment Epitheliopathy 18 0.023
908
VRT001 Vertebral Artery Occlusion 18 0.023
909
MSN002 Mesenteric Lymphadenitis 18 0.023
910
PLY004 Polyp of Corpus Uteri 18 0.023
911
THR020 Thrombophilia Due to Heparin Cofactor Ii Deficiency 17 0.023
912
c MLT009 Multiple Cranial Nerve Palsy 18 0.023
913
HMC012 Hemicrania Continua 17 0.023
914
FRN014 Fournier Gangrene 17 0.023
915
QLT001 Qualitative Platelet Defect 16 0.023
916
ART109 Arterial Thoracic Outlet Syndrome 17 0.023
917
SBC002 Subclavian Artery Aneurysm 16 0.023
918
P HMN004 Hemangioma of Liver 17 0.023
919
48X002 48,xxxy Syndrome 16 0.023
920
RSS023 Resistance to Clopidogrel 16 0.023
921
BNT001 Banti's Syndrome 16 0.023
922
FXL001 Foix-Alajouanine Syndrome 16 0.023
923
MSN003 Mesenteric Vascular Occlusion 16 0.023
924
PLS001 Pulsating Exophthalmos 16 0.023
925
PNT023 Pontine Hemorrhage 16 0.023
926
CNT067 Central Cord Syndrome 16 0.023
927
HYP015 Hyperlucent Lung 16 0.023
928
ANG062 Angioosteohypertrophic Syndrome 15 0.023
929
SCT001 Sciatic Neuropathy 15 0.023
930
CNG298 Congenital Pancreatic Cyst 15 0.023
931
AMP007 Amphetamine Abuse 14 0.023
932
CHR076 Choriocarcinoma of the Testis 15 0.023
933
THR068 Thrombophilia Due to Protein C Deficiency, Autosomal Recessive 14 0.023
934
XLN139 X-Linked Intellectual Disability - Macrocephaly - Macroorchidism 15 0.023
935
CNG092 Congenital Extrahepatic Portosystemic Shunt 14 0.023
936
DRL001 Dural Sinus Malformation 14 0.023
937
GST016 Gastric Signet Ring Cell Adenocarcinoma 13 0.023
938
TMP006 Temporomandibular Ankylosis 13 0.023
939
THR021 Thrombophilia Due to Hrg Deficiency 12 0.023
940
c THR060 Thrombophilia, Familial, Due to Decreased Release of Plat 12 0.023
941
CGH002 Cough Headache 13 0.023
942
RNL001 Renal Artery Obstruction 12 0.023
943
PLM062 Pulmonary Hyalinizing Granuloma 12 0.023
944
MTH028 Mthfr Thermolabile Variant 11 0.023
945
CNG171 Congenital Plasminogen Deficiency 11 0.023
946
CYS035 Cystic Adventitial Disease 11 0.023
947
CVR001 Cavernous Sinus Meningioma 11 0.023
948
INF001 Infarct of Liver 10 0.023
949
INT055 Intravascular Fasciitis 9 0.023
950
c PRT053 Portal Hypertension Due to Infrahepatic Block 3 0.023