Search results for "thrombosis"

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

1076 hits were found for 'thrombosis'

# Family MCID Name MIFTS Score
1
SGT001 Sagittal Sinus Thrombosis 49 6.153
2
PRT018 Portal Vein Thrombosis 54 5.340
3
CRN017 Coronary Thrombosis 60 5.278
4
LTR002 Lateral Sinus Thrombosis 25 5.156
5
VNS009 Venous Thrombosis 59 5.120
6
INT078 Intracranial Thrombosis 32 4.775
7
CVR002 Cavernous Sinus Thrombosis 27 4.561
8
CRT004 Carotid Artery Thrombosis 46 3.977
9
HPT002 Hepatic Vein Thrombosis 66 3.895
10
INT076 Intracranial Sinus Thrombosis 15 3.162
11
CRB132 Cerebral Sinovenous Thrombosis 42 2.868
12
VNS011 Venous Thrombosis, Protection Against 18 2.556
13
WRF005 Warfarine Dose Selection in the Treatment of Venous Thrombosis and Atrial Fibrillation 14 2.530
14
THR062 Thrombosis, Hyperhomocysteinemic 12 2.530
15
DPV002 Deep Venous Thrombosis, Protection Against 6 2.530
16
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 5 2.530
17
RSS009 Resistance to Acenocoumarol in Venous Thrombosis and Atrial Fibrillation 4 2.530
18
RSS010 Resistance to Warfarine in Venous Thrombosis and Atrial Fibrillation 4 2.530
19
RSS015 Resistance to Phenprocoumon in Venous Thrombosis and Atrial Fibrillation 4 2.530
20
RSS018 Resistance to Fluindione in Venous Thrombosis and Atrial Fibrillation 4 2.530
21
MND006 Mondor Disease 19 1.821
22
VNS012 Venous Thoracic Outlet Syndrome 19 1.789
23
CRB009 Cerebritis 38 0.508
24
c HPT021 Hepatitis 63 0.271
25
PRT014 Protein S Deficiency 64 0.266
26
P THR015 Thrombophilia 66 0.260
27
P MYC007 Myocardial Infarction 92 0.260
28
PLM033 Pulmonary Embolism 65 0.243
29
c THR014 Thrombocytopenia 69 0.240
30
HPR003 Heparin-Induced Thrombocytopenia 53 0.235
31
PRT011 Protein C Deficiency 55 0.229
32
ANT006 Antiphospholipid Syndrome 68 0.227
33
P HYP075 Hypertension 85 0.197
34
ANR040 Aneurysm 45 0.195
35
THR079 Thromboembolism 67 0.183
36
HPT023 Hepatocellular Carcinoma 54 0.180
37
P SYS001 Systemic Lupus Erythematosus 89 0.176
38
ANT009 Antithrombin Iii Deficiency 58 0.176
39
c LPS004 Lupus Erythematosus 75 0.175
40
HYP037 Hyperhomocysteinemia 52 0.173
41
END072 Endotheliitis 50 0.169
42
c ESS003 Essential Thrombocythemia 61 0.164
43
c NPH012 Nephrotic Syndrome 67 0.158
44
c ACT075 Acute Myocardial Infarction 59 0.145
45
P LKM002 Leukemia 76 0.144
46
c PNC044 Pancreatitis 68 0.140
47
CLT003 Colitis 64 0.138
48
VNS010 Venous Thromboembolism 54 0.138
49
THR016 Thrombophlebitis 68 0.137
50
PLY001 Polycythemia Vera 85 0.135
51
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 54 0.135
52
HMG002 Hemoglobinuria 51 0.135
53
ULC004 Ulcerative Colitis 64 0.133
54
c PLY018 Polycythemia 59 0.133
55
HDC001 Headache 57 0.129
56
P PRT013 Portal Hypertension 65 0.127
57
ART111 Artery Disease 63 0.125
58
LVR012 Liver Cirrhosis 76 0.123
59
ATH003 Atherosclerosis 68 0.123
60
P SNS014 Sinusitis 57 0.121
61
DSS009 Disseminated Intravascular Coagulation 61 0.115
62
RTN023 Retinitis 53 0.115
63
c MNN013 Meningitis 67 0.113
64
THR004 Thrombocytosis 60 0.111
65
c INF037 Inflammatory Bowel Disease 43 0.111
66
PRP030 Purpura 65 0.109
67
INT003 Intracranial Hypotension 30 0.109
68
DYS026 Dysfibrinogenemia 62 0.106
69
CLL003 Cellulitis 58 0.106
70
P HYP098 Hypereosinophilic Syndrome 61 0.104
71
OTT002 Otitis Media 58 0.104
72
HDN002 Head Injury 48 0.104
73
THR013 Thoracic Outlet Syndrome 52 0.102
74
P ART084 Arteriovenous Fistula 46 0.102
75
ISC004 Ischemia 62 0.099
76
P HMC002 Homocystinuria 59 0.099
77
OVR029 Ovarian Hyperstimulation Syndrome 67 0.097
78
FCT004 Factor Xii Deficiency 66 0.094
79
INT075 Intracranial Hypertension 52 0.094
80
PST095 Post-Thrombotic Syndrome 42 0.094
81
PSD002 Pseudotumor Cerebri 56 0.091
82
BLN003 Blindness 52 0.091
83
TBR010 Tuberculosis 85 0.086
84
P OBS005 Obesity 89 0.083
85
c ACT027 Acute Pancreatitis 63 0.083
86
PRG060 Pregnancy Loss 47 0.083
87
FCT007 Factor Vii Deficiency 80 0.080
88
THR006 Thromboangiitis Obliterans 79 0.080
89
CRH001 Crohn's Disease 75 0.080
90
c DBT009 Diabetes Mellitus 73 0.080
91
c PLM037 Pulmonary Hypertension 73 0.080
92
c HMP007 Hemophilia 64 0.080
93
DFC004 Deficiency Anemia 62 0.080
94
MYM001 Myoma 55 0.080
95
PPL021 Papilledema 53 0.080
96
CTS005 Catastrophic Antiphospholipid Syndrome 51 0.080
97
CRD137 Cardiogenic Shock 48 0.080
98
SPR035 Superior Vena Cava Syndrome 39 0.080
99
ACT119 Acute Promyelocytic Leukemia 68 0.077
100
CRB039 Cerebrovascular Disease 68 0.077
101
IRN001 Iron Deficiency Anemia 56 0.077
102
CRN006 Coronary Aneurysm 49 0.077
103
CYT008 Cytomegalovirus Infection 43 0.077
104
SPL006 Splenic Infarction 38 0.077
105
LMR001 Lemierre's Syndrome 32 0.077
106
ORB006 Orbital Cellulitis 30 0.077
107
BHC002 Behcet's Disease 79 0.074
108
P MYL005 Myelofibrosis 74 0.074
109
VSC007 Vascular Disease 69 0.074
110
STR067 Stroke, Ischemic 64 0.074
111
PTN001 Patent Foramen Ovale 61 0.074
112
P ADN016 Adenocarcinoma 58 0.074
113
P RTN022 Retinal Vein Occlusion 56 0.074
114
c OST028 Osteochondroma 54 0.074
115
SYN053 Syndromic Diarrhea 34 0.074
116
ANK002 Ankylosing Spondylitis 76 0.070
117
P ANG001 Angelman Syndrome 71 0.070
118
P HYD006 Hydrocephalus 69 0.070
119
P GLM007 Glomerulonephritis 68 0.070
120
ACN002 Acanthosis Nigricans 64 0.070
121
P ACT101 Acute Lymphoblastic Leukemia 64 0.070
122
ART019 Aortic Valve Stenosis 63 0.070
123
P RNL014 Renal Cell Carcinoma 63 0.070
124
c AFB001 Afibrinogenemia 63 0.070
125
P CRV039 Cervicitis 57 0.070
126
c CNT016 Central Retinal Vein Occlusion 57 0.070
127
c RTN014 Retinal Artery Occlusion 57 0.070
128
c LYM026 Lymphoblastic Leukemia 56 0.070
129
P HYP083 Hypopituitarism 52 0.070
130
MMB002 Membranous Glomerulonephritis 52 0.070
131
P ATX010 Ataxia Neuropathy Spectrum 47 0.070
132
P LVR011 Liver Cancer 90 0.067
133
PRT036 Peritonitis 71 0.067
134
VNW001 Von Willebrand's Disease 71 0.067
135
SPS077 Sepsis 69 0.067
136
P THR090 Thrombocythemia 1 58 0.067
137
THY033 Thyrotoxicosis 57 0.067
138
HLL004 Hellp Syndrome 53 0.067
139
HMC014 Homocysteinemia 48 0.067
140
CHY006 Chylous Ascites 48 0.067
141
VRC005 Varicose Veins 45 0.067
142
THR035 Thrombasthenia 44 0.067
143
CRT015 Carotid Artery Occlusion 44 0.067
144
SPN185 Spinal Cord Infarction 42 0.067
145
P BRS047 Breast Cancer 85 0.063
146
CDS001 Cadasil 84 0.063
147
P HMP004 Hemophilia B 80 0.063
148
P PRC016 Pre-Eclampsia 79 0.063
149
KWS002 Kawasaki Disease 75 0.063
150
P ART022 Arthritis 74 0.063
151
c THL005 Thalassemia 71 0.063
152
ART016 Aortic Aneurysm 70 0.063
153
SRC014 Sarcoma 68 0.063
154
P HRD011 Hereditary Spherocytosis 68 0.063
155
P LVR013 Liver Disease 68 0.063
156
FCT006 Factor V Deficiency 66 0.063
157
VSC011 Vasculitis 65 0.063
158
FCT002 Factor Xi Deficiency 64 0.063
159
c ECL001 Eclampsia 63 0.063
160
c HYP076 Hyperthyroidism 62 0.063
161
ART005 Arteriovenous Malformation 62 0.063
162
SCK005 Sickle Cell Disease 61 0.063
163
SND002 Sneddon Syndrome 60 0.063
164
c ISC002 Ischemic Optic Neuropathy 57 0.063
165
P END033 Endocarditis 56 0.063
166
P INT030 Intracranial Aneurysm 56 0.063
167
ART001 Arterial Tortuosity Syndrome 55 0.063
168
P CNT028 Central Retinal Artery Occlusion 52 0.063
169
ISC015 Ischemic Colitis 52 0.063
170
NNT024 Neonatal Stroke 50 0.063
171
ANG054 Angina Pectoris 46 0.063
172
EVN001 Evans' Syndrome 45 0.063
173
BRS090 Breast Reconstruction 44 0.063
174
BRN026 Branch Retinal Artery Occlusion 43 0.063
175
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 43 0.063
176
P CRN074 Coronary Artery Aneurysm 40 0.063
177
FCT013 Factor V Leiden Thrombophilia 34 0.063
178
SPH007 Sphenoid Sinusitis 25 0.063
179
MYT019 May-Thurner Syndrome 14 0.063
180
P ATX002 Ataxia Telangiectasia 87 0.059
181
P APL001 Aplastic Anemia 84 0.059
182
MYL040 Myelodysplastic Syndromes 79 0.059
183
c MYL006 Myeloid Leukemia 74 0.059
184
LGG001 Legg-Calve-Perthes Disease 66 0.059
185
P HPT001 Hepatitis C 66 0.059
186
P ESN007 Eosinophilia 62 0.059
187
NRP001 Neuropathy 61 0.059
188
SPH001 Sapho Syndrome 60 0.059
189
CHL067 Cholecystitis 60 0.059
190
P ANT058 Anterior Ischemic Optic Neuropathy 58 0.059
191
c ACT073 Acute Leukemia 56 0.059
192
AND003 Andersen-Tawil Syndrome 53 0.059
193
BRN106 Burns 49 0.059
194
BCT015 Bacteremia 49 0.059
195
MNN021 Meningococcemia 48 0.059
196
P VNS003 Venous Insufficiency 47 0.059
197
CHR466 Chronic Thromboembolic Pulmonary Hypertension 43 0.059
198
SPP008 Suppurative Otitis Media 41 0.059
199
c ACQ012 Acquired Angioedema 41 0.059
200
PRP028 Peripheral Vertigo 40 0.059
201
PTR001 Petrositis 28 0.059
202
HGH021 Hughes-Stovin Syndrome 22 0.059
203
P LPR003 Leprosy 77 0.054
204
P PNM007 Pneumonia 77 0.054
205
GLN003 Glanzmann's Thrombasthenia 76 0.054
206
RLP001 Relapsing Polychondritis 72 0.054
207
c HYP095 Hypercholesterolemia 72 0.054
208
c HPT016 Hepatitis B 68 0.054
209
ART021 Arteriosclerosis 67 0.054
210
P ABD003 Abdominal Aortic Aneurysm 67 0.054
211
DBT001 Diabetic Ketoacidosis 67 0.054
212
FCT003 Factor X Deficiency 65 0.054
213
BLR001 Biliary Atresia 65 0.054
214
SPN186 Spinal Cord Injury 61 0.054
215
SPT013 Septic Shock 60 0.054
216
PRP007 Priapism 59 0.054
217
c THR005 Thrombotic Thrombocytopenic Purpura 58 0.054
218
HYP063 Hypersplenism 58 0.054
219
P CNG019 Congenital Afibrinogenemia 57 0.054
220
TYP013 Type 1 Von Willebrand Disease 56 0.054
221
HPT019 Hepatic Encephalopathy 56 0.054
222
c MNT147 Mental Retardation 56 0.054
223
P CMP008 Compartment Syndrome 55 0.054
224
PRT019 Protein-Losing Enteropathy 55 0.054
225
c ACR001 Aicardi-Goutieres Syndrome 54 0.054
226
c ACQ014 Acquired Hemophilia 51 0.054
227
MLK003 Melkersson-Rosenthal Syndrome 51 0.054
228
RTR011 Retroperitoneal Fibrosis 50 0.054
229
FCT005 Factor Xiii Deficiency 50 0.054
230
ACT099 Acute Fatty Liver of Pregnancy 49 0.054
231
ERY004 Erysipelas 49 0.054
232
ABD004 Abdominal Tuberculosis 46 0.054
233
MDS022 Mediastinitis 45 0.054
234
VND001 Vein Disease 44 0.054
235
BLD054 Blood Protein Disease 37 0.054
236
INF133 Inferior Vena Cava Interruption 34 0.054
237
PRX023 Paroxysmal Nocturnal Hemoglobinuria, Somatic 32 0.054
238
HMC004 Homocysteine Plasma Level 32 0.054
239
MTH044 Mthfr Gene Mutation 32 0.054
240
CNG058 Congenital Antithrombin Deficiency Type 3 32 0.054
241
c FRN011 Frontal Sinusitis 29 0.054
242
SBD001 Subdural Empyema 27 0.054
243
THR089 Thrombophilia Due to Protein S Deficiency, Autosomal Dominant 26 0.054
244
c BNG076 Benign Exophthalmos Syndrome 22 0.054
245
HRD083 Hereditary Antithrombin Deficiency 21 0.054
246
c THR023 Thrombophilia Due to Thrombomodulin Defect 10 0.054
247
HDG007 Hodgkin's Lymphoma 93 0.050
248
SCK003 Sickle Cell Anemia 84 0.050
249
P PHC003 Pheochromocytoma 82 0.050
250
AND002 Androgen Insensitivity Syndrome 80 0.050
251
P LNG032 Lung Cancer 78 0.050
252
BRK003 Burkitt's Lymphoma 77 0.050
253
P FML018 Familial Mediterranean Fever 75 0.050
254
FCT001 Factor Viii Deficiency 74 0.050
255
ASP006 Aspergillosis 72 0.050
256
P TMP003 Temporal Arteritis 72 0.050
257
ACQ007 Acquired Immunodeficiency Syndrome 70 0.050
258
c AXN002 Axenfeld-Rieger Syndrome 69 0.050
259
P CNG401 Congenital Heart Disease 69 0.050
260
GST009 Gastroschisis 66 0.050
261
c HML002 Hemolytic Anemia 65 0.050
262
P BRN019 Bernard-Soulier Syndrome 64 0.050
263
P CLN016 Colon Cancer 64 0.050
264
c INT070 Intestinal Obstruction 62 0.050
265
P LMY004 Leiomyosarcoma 61 0.050
266
ADR015 Adrenocortical Carcinoma 61 0.050
267
c MYL007 Myeloma 60 0.050
268
PRS047 Prostatitis 59 0.050
269
MYC002 Mycobacterium Avium Complex Disease 58 0.050
270
ANR004 Anuria 58 0.050
271
OST017 Osteomyelitis 58 0.050
272
NDL013 Nodular Regenerative Hyperplasia 57 0.050
273
CHR001 Churg-Strauss Syndrome 57 0.050
274
DDN006 Duodenitis 55 0.050
275
APP008 Appendicitis 55 0.050
276
KLN001 Klinefelter's Syndrome 55 0.050
277
MYL001 Myelitis 54 0.050
278
P PYL005 Pyelonephritis 54 0.050
279
CHL069 Cholesteatoma 54 0.050
280
NPH051 Nephritis 53 0.050
281
EXS001 Exostosis 51 0.050
282
NNR007 Non-Arteritic Anterior Ischemic Optic Neuropathy 50 0.050
283
c SVR056 Severe Hemophilia a 49 0.050
284
FSC004 Fasciitis 45 0.050
285
ART110 Arteritic Anterior Ischemic Optic Neuropathy 44 0.050
286
ZYG002 Zygomycosis 44 0.050
287
CRT012 Cortical Blindness 43 0.050
288
CDQ001 Cauda Equina Syndrome 41 0.050
289
LCK001 Locked-in Syndrome 41 0.050
290
AMR003 Amaurosis Fugax 40 0.050
291
PRP080 Peripheral Artery Disease 35 0.050
292
AND005 Androgen Insensitivity Syndrome, Mild 21 0.050
293
HMC030 Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency 19 0.050
294
ORB016 Orbital Varix 14 0.050
295
P FML021 Familial Hypercholesterolemia 85 0.044
296
P MLT020 Multiple Sclerosis 84 0.044
297
c BTT002 Beta Thalassemia 82 0.044
298
TTR001 Tetralogy of Fallot 74 0.044
299
P WGN002 Wegener's Granulomatosis 73 0.044
300
c CHR065 Chronic Myeloid Leukemia 73 0.044
301
SCH014 Schistosomiasis 72 0.044
302
c ACT074 Acute Lymphocytic Leukemia 69 0.044
303
MRB003 Morbid Obesity 67 0.044
304
P ATM010 Autoimmune Hemolytic Anemia 66 0.044
305
P GRV001 Graves' Disease 64 0.044
306
P ESP024 Esophagitis 63 0.044
307
CRN036 Craniopharyngioma 62 0.044
308
c KDN018 Kidney Disease 62 0.044
309
TYP007 Typhoid Fever 62 0.044
310
P SCH018 Schizencephaly 61 0.044
311
CHR074 Choriocarcinoma 60 0.044
312
P END047 Endophthalmitis 59 0.044
313
c SLP006 Sleep Apnea 59 0.044
314
URM002 Uremia 57 0.044
315
P HMR012 Hemorrhagic Fever 57 0.044
316
INT007 Intermediate Coronary Syndrome 56 0.044
317
RDC002 Radiculopathy 55 0.044
318
PNM013 Pneumococcal Meningitis 55 0.044
319
CRD001 Cardiac Tamponade 54 0.044
320
INT002 Intermittent Claudication 54 0.044
321
P PND001 Pain Disorder 54 0.044
322
ANG011 Angiodysplasia 54 0.044
323
c ACT134 Acute Liver Failure 53 0.044
324
SPT004 Septic Arthritis 53 0.044
325
LPS007 Lupus Nephritis 52 0.044
326
PRC013 Pericarditis 52 0.044
327
HMR002 Hemarthrosis 51 0.044
328
ANG018 Angiomyolipoma 51 0.044
329
VRC001 Varicocele 50 0.044
330
CRN020 Coronary Restenosis 50 0.044
331
CCN002 Cocaine Abuse 50 0.044
332
c ERY013 Erythrocytosis 50 0.044
333
OPT009 Optic Neuritis 49 0.044
334
NRT004 Neuritis 49 0.044
335
SPN035 Spindle Cell Sarcoma 49 0.044
336
CHL004 Cholelithiasis 47 0.044
337
MYC020 Mycobacterium Tuberculosis, Susceptibility to Infection by 47 0.044
338
c PRN026 Porencephaly 47 0.044
339
VTM002 Vitamin B12 Deficiency 47 0.044
340
LYM021 Lymphadenitis 47 0.044
341
ACT055 Actinomycosis 46 0.044
342
ACQ017 Acquired Von Willebrand Syndrome 46 0.044
343
PRT093 Proteus Syndrome, Somatic 46 0.044
344
ESN011 Eisenmenger Syndrome 44 0.044
345
NRN002 Neuronitis 43 0.044
346
NPH017 Nephrosis 42 0.044
347
c CHR431 Chronic Venous Insufficiency 38 0.044
348
SCR015 Scarlet Fever 37 0.044
349
IMM088 Immunodeficiency 36 36 0.044
350
HMR001 Hemorrhagic Thrombocythemia 34 0.044
351
HMC020 Homocystinuria, B6-Responsive and Nonresponsive Types 33 0.044
352
VNF001 Vein of Galen Aneurysm 31 0.044
353
PRT045 Prothrombin-Related Thrombophilia 30 0.044
354
IRN002 Iron Metabolism Disease 27 0.044
355
THR067 Thrombophilia Due to Protein C Deficiency, Autosomal Dominant 25 0.044
356
SHW001 Shwartzman Phenomenon 25 0.044
357
THN005 Thunderclap Headache 18 0.044
358
DBL009 Double Inferior Vena Cava 18 0.044
359
c ACT061 Acute Sphenoidal Sinusitis 17 0.044
360
THR088 Thrombophilia Due to Protein S Deficiency, Autosomal Recessive 10 0.044
361
CYS001 Cystic Fibrosis 96 0.038
362
P RHM011 Rheumatoid Arthritis 94 0.038
363
P ACT019 Acute Myeloid Leukemia 92 0.038
364
P CHR090 Chronic Lymphocytic Leukemia 88 0.038
365
P MLT019 Multiple Myeloma 88 0.038
366
P OVR042 Ovarian Cancer 84 0.038
367
P PRM021 Primary Pulmonary Hypertension 80 0.038
368
P CLC005 Celiac Disease 74 0.038
369
P AST007 Astrocytoma 72 0.038
370
KLP002 Klippel-Trenaunay Syndrome 69 0.038
371
GSG001 Gas Gangrene 67 0.038
372
PRP027 Peripheral Vascular Disease 67 0.038
373
P TRN020 Turner Syndrome 67 0.038
374
c THY032 Thyroiditis 65 0.038
375
PHR003 Pharyngitis 65 0.038
376
DRM006 Dermatitis 65 0.038
377
c ENC004 Encephalitis 65 0.038
378
P MLN008 Melanoma 64 0.038
379
c VRL010 Viral Hepatitis 63 0.038
380
c MLG069 Malignant Hypertension 63 0.038
381
P MTR012 Mitral Valve Disease 62 0.038
382
VGN023 Vaginitis 62 0.038
383
HYD012 Hydrops Fetalis 61 0.038
384
HYP066 Hyperglycemia 61 0.038
385
P CNJ013 Conjunctivitis 61 0.038
386
P RNV001 Renovascular Hypertension 61 0.038
387
c ALM001 Al Amyloidosis 60 0.038
388
P LPS002 Liposarcoma 60 0.038
389
CHC001 Chickenpox 59 0.038
390
PLY041 Polymyositis 58 0.038
391
CRY004 Cryoglobulinemia 58 0.038
392
LYM019 Lymphosarcoma 58 0.038
393
BRN029 Brain Disease 57 0.038
394
PRT039 Proteinuria 57 0.038
395
P MYM002 Moyamoya Disease 57 0.038
396
BRN071 Brain Injury 57 0.038
397
P BCL006 B-Cell Lymphomas 56 0.038
398
PRN011 Pernicious Anemia 55 0.038
399
EBS001 Ebstein Anomaly 55 0.038
400
OCL006 Ocular Hypertension 54 0.038
401
P EXP004 Exophthalmos 54 0.038
402
HST009 Histiocytoma 54 0.038
403
NPH011 Nephroblastoma 54 0.038
404
c OPH004 Ophthalmoplegia 54 0.038
405
BNM001 Bone Marrow Cancer 54 0.038
406
TRM010 Traumatic Brain Injury 53 0.038
407
c LYM025 Lymphedema 52 0.038
408
MNN014 Mononeuritis 51 0.038
409
LPD004 Lipoid Nephrosis 50 0.038
410
P SZR006 Seizure Disorder 50 0.038
411
P CHR092 Chronic Myeloproliferative Disease 49 0.038
412
TRN007 Transsexualism 49 0.038
413
c SVR005 Severe Pre-Eclampsia 49 0.038
414
P PNC001 Pancytopenia 48 0.038
415
DYS157 Dysplasminogenemia 47 0.038
416
PRP016 Paraplegia 47 0.038
417
c HPT073 Hepatitis C Virus 47 0.038
418
RTN021 Retinal Vascular Occlusion 47 0.038
419
END021 Endomyocardial Fibrosis 46 0.038
420
SPL018 Splenomegaly 46 0.038
421
LMB062 Limb Ischemia 46 0.038
422
P HMG003 Hemoglobin E Disease 45 0.038
423
CRP018 Cor Pulmonale 44 0.038
424
PLS018 Plasminogen Activator Inhibitor Type 1 Deficiency 43 0.038
425
OBS004 Obstructive Hydrocephalus 42 0.038
426
c ACT042 Acute Pyelonephritis 42 0.038
427
EPD005 Epidural Abscess 42 0.038
428
CNT060 Central Serous Chorioretinopathy 41 0.038
429
HNC001 Henoch-Schoenlein Purpura 41 0.038
430
TYP015 Type 2b Von Willebrand Disease 40 0.038
431
INF013 Inferior Myocardial Infarction 40 0.038
432
TRC023 Trichinosis 39 0.038
433
BNM005 Bone Marrow Necrosis 39 0.038
434
CRB086 Cerebral Aneurysms 38 0.038
435
BCK006 Back Pain 38 0.038
436
PRS045 Prostatic Hypertrophy 37 0.038
437
HNS001 Hansen's Disease 37 0.038
438
STR044 Steroid-Resistant Nephrotic Syndrome 36 0.038
439
NRS005 Neurosarcoidosis 35 0.038
440
HYP319 Hypereosinophilic Syndrome, Idiopathic, Resistant to Imatinib 34 0.038
441
INT221 Intravascular Large B-Cell Lymphoma 34 0.038
442
P LBY004 Labyrinthitis 33 0.038
443
P INF069 Infantile Neuroaxonal Dystrophy 1 33 0.038
444
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 33 0.038
445
LYM014 Lymphangitis 33 0.038
446
P CRN035 Cranial Nerve Palsy 31 0.038
447
TYP018 Type 3 Von Willebrand Disease 30 0.038
448
c TWN006 Twin Twin Transfusion Syndrome 29 0.038
449
ALX001 Alexia 28 0.038
450
BSL004 Basilar Artery Occlusion 28 0.038
451
P HYP589 Hypodysfibrinogenemia 26 0.038
452
ETH009 Ethmoid Sinusitis 26 0.038
453
CHR158 Charles Bonnet Syndrome 26 0.038
454
PL2001 Pla2g6-Associated Neurodegeneration 24 0.038
455
ART007 Aorta Atresia 22 0.038
456
ABD009 Abducens Palsy 21 0.038
457
THR007 Thrombophlebitis Migrans 21 0.038
458
PRN017 Perianal Hematoma 13 0.038
459
CNG056 Congenital Antithrombin Deficiency 12 0.038
460
P ALZ001 Alzheimer's Disease 98 0.031
461
P TYP008 Type 1 Diabetes Mellitus 95 0.031
462
P PNC035 Pancreatic Cancer 92 0.031
463
P FML011 Familial Adenomatous Polyposis 89 0.031
464
P LFR001 Li-Fraumeni Syndrome 88 0.031
465
P TBR001 Tuberous Sclerosis 86 0.031
466
GLC006 Galactosemia 85 0.031
467
P MDL005 Medulloblastoma 80 0.031
468
P MNN012 Meningioma 78 0.031
469
P CLR023 Colorectal Cancer 77 0.031
470
P MST009 Mastocytosis 75 0.031
471
P PRD006 Prader-Willi Syndrome 73 0.031
472
c PRM002 Primary Hyperoxaluria 73 0.031
473
NNH001 Non-Hodgkin Lymphoma 72 0.031
474
GLL008 Gilles De La Tourette Syndrome 72 0.031
475
OBS002 Obsessive-Compulsive Disorder 71 0.031
476
P MGR002 Migraine 71 0.031
477
P DRM010 Dermatomyositis 71 0.031
478
CCC001 Coccidioidomycosis 71 0.031
479
P HMN010 Hemangioma 70 0.031
480
P NRB001 Neuroblastoma 70 0.031
481
CHL065 Cholangiocarcinoma 69 0.031
482
NRL016 Neural Tube Defects 69 0.031
483
P KDN017 Kidney Cancer 69 0.031
484
PLY017 Polyarteritis Nodosa 69 0.031
485
ATM004 Autoimmune Thrombocytopenic Purpura 69 0.031
486
P END044 Endometriosis 69 0.031
487
P PRD008 Periodontitis 68 0.031
488
TKY001 Takayasu's Arteritis 68 0.031
489
SCR008 Scrub Typhus 68 0.031
490
c HYP086 Hypothyroidism 68 0.031
491
P PLY011 Polycystic Ovary Syndrome 67 0.031
492
CRY005 Cryptococcosis 67 0.031
493
ERD001 Erdheim-Chester Disease 67 0.031
494
OLL001 Ollier Disease 66 0.031
495
P HYP056 Hypoglycemia 66 0.031
496
P ANR007 Anorexia Nervosa 65 0.031
497
MLG056 Malignant Hyperthermia 65 0.031
498
P GST044 Gastritis 65 0.031
499
STT001 Status Epilepticus 65 0.031
500
DBN001 Dubin-Johnson Syndrome 65 0.031
501
P CRN018 Coronary Artery Anomaly 65 0.031
502
ADN018 Adenoma 65 0.031
503
P DYS007 Dyskeratosis Congenita 65 0.031
504
c SYS004 Systemic Mastocytosis 64 0.031
505
P INS005 Insulin Resistance 64 0.031
506
PMS001 Poems Syndrome 64 0.031
507
c HYP061 Hypertrophic Cardiomyopathy 64 0.031
508
P HRD057 Hereditary Pancreatitis 64 0.031
509
CRB037 Cerebral Palsy 64 0.031
510
c EHL001 Ehlers-Danlos Syndrome 63 0.031
511
P ERY008 Erythromelalgia 63 0.031
512
CLN045 Colonic Benign Neoplasm 63 0.031
513
P OLG002 Oligodendroglioma 62 0.031
514
P CRB042 Cerebellar Ataxia 62 0.031
515
P CMP010 Complex Regional Pain Syndrome 62 0.031
516
ART031 Aortic Coarctation 62 0.031
517
CYS005 Cysticercosis 62 0.031
518
P RBL001 Rubella 62 0.031
519
ADL030 Adult-Onset Still's Disease 62 0.031
520
P ANP001 Anaplastic Large Cell Lymphoma 62 0.031
521
c PLY014 Polycystic Kidney Disease 61 0.031
522
c MSC005 Muscular Dystrophy 61 0.031
523
P MYP004 Myopathy 61 0.031
524
MYL020 Myelomeningocele 61 0.031
525
TXC005 Toxic Shock Syndrome 61 0.031
526
DWN001 Down Syndrome 61 0.031
527
P CRV035 Cervical Cancer 60 0.031
528
GNG013 Gingivitis 60 0.031
529
ASP003 Aseptic Meningitis 60 0.031
530
PLM001 Pulmonary Tuberculosis 60 0.031
531
c ANG015 Angioedema 60 0.031
532
P HYP080 Hypogonadism 59 0.031
533
c HPT003 Hepatitis a 58 0.031
534
P GLB002 Glioblastoma 58 0.031
535
CVR006 Cavernous Hemangioma 58 0.031
536
RHB003 Rhabdomyosarcoma 58 0.031
537
c ATX004 Ataxia 58 0.031
538
CNN005 Connective Tissue Disease 58 0.031
539
PRC012 Pericardial Effusion 57 0.031
540
c MLG002 Malignant Peritoneal Mesothelioma 57 0.031
541
P MYC008 Myocarditis 57 0.031
542
CCT002 Cicatricial Pemphigoid 57 0.031
543
P DBT005 Diabetes Insipidus 57 0.031
544
GLB015 Glioblastoma Multiforme 57 0.031
545
HYP266 Hypoxia 57 0.031
546
c CTR002 Cataract 57 0.031
547
TNS005 Tonsillitis 56 0.031
548
PLS011 Plasmacytoma 56 0.031
549
ACT017 Acute Chest Syndrome 56 0.031
550
c HPT015 Hepatitis D 56 0.031
551
P PLC011 Pilocytic Astrocytoma 56 0.031
552
PYD001 Pyoderma Gangrenosum 56 0.031
553
MLG077 Malignant Peripheral Nerve Sheath Tumor 56 0.031
554
MCR088 Microscopic Polyangiitis 56 0.031
555
P SYR001 Syringomyelia 55 0.031
556
TYP011 Typhus 55 0.031
557
BRN004 Brain Edema 54 0.031
558
P CHL066 Cholangitis 54 0.031
559
P HMN013 Hemangiopericytoma 54 0.031
560
LYM040 Lymphoblastic Lymphoma 53 0.031
561
ATP002 Atopy 53 0.031
562
HPT032 Hepatocellular Carcinoma, Somatic 53 0.031
563
END031 Endometrial Stromal Sarcoma 53 0.031
564
P ENC008 Encephalocele 53 0.031
565
CRV031 Cervical Adenocarcinoma 52 0.031
566
STS002 Situs Inversus 52 0.031
567
HMP005 Hemiplegia 52 0.031
568
CRN014 Cronkhite-Canada Syndrome 52 0.031
569
TRN015 Transient Cerebral Ischemia 52 0.031
570
RFL001 Reflex Sympathetic Dystrophy 52 0.031
571
c HYD002 Hydronephrosis 52 0.031
572
DGS001 Degos Disease 51 0.031
573
ALC009 Alcoholic Liver Cirrhosis 51 0.031
574
PYD002 Pyoderma 51 0.031
575
PLV003 Pelvic Inflammatory Disease 50 0.031
576
SCT005 Scott Syndrome 50 0.031
577
OBS001 Obstructive Jaundice 50 0.031
578
P APL006 Aplasia Cutis Congenita 50 0.031
579
c NNT009 Neonatal Diabetes Mellitus 50 0.031
580
SYN006 Synovial Sarcoma 50 0.031
581
CYS009 Cystadenoma 50 0.031
582
PLC007 Placental Abruption 50 0.031
583
CLS010 Cluster Headache 50 0.031
584
GRM009 Germ Cell Tumors 49 0.031
585
c BCT007 Bacterial Meningitis 49 0.031
586
P PRT096 Peritoneal Mesothelioma 49 0.031
587
c PSD003 Pseudohypoaldosteronism 49 0.031
588
SFT003 Soft Tissue Sarcoma 49 0.031
589
SMN007 Seminoma 49 0.031
590
PYM001 Pyomyositis 48 0.031
591
MTS001 Mutism 48 0.031
592
P WRF002 Warfarin Sensitivity 48 0.031
593
PNV001 Panuveitis 48 0.031
594
BLD034 Bile Duct Carcinoma 47 0.031
595
CNS002 Constrictive Pericarditis 47 0.031
596
P OVR046 Ovarian Cyst 47 0.031
597
URT010 Ureteral Obstruction 46 0.031
598
PNN001 Panniculitis 46 0.031
599
SPL004 Splenic Marginal Zone Lymphoma 46 0.031
600
P CRT018 Carotid Intimal Medial Thickness 46 0.031
601
P MYH004 Myh9 Related Thrombocytopenia 46 0.031
602
HPT008 Hepatic Tuberculosis 46 0.031
603
P ATR005 Atrophic Gastritis 46 0.031
604
P HMR005 Hemorrhoid 46 0.031
605
LYM012 Lymphoplasmacytic Lymphoma 46 0.031
606
PNH001 Panhypopituitarism 45 0.031
607
HMN016 Hemangioendothelioma 45 0.031
608
PLR007 Pleural Empyema 44 0.031
609
c PNC102 Pancreatitis, Chronic 44 0.031
610
ILS001 Ileus 44 0.031
611
SYS011 Systemic Lupus Erythematosus, Association with 44 0.031
612
LNG029 Lung Adenocarcinoma 43 0.031
613
ILC002 Ileocolitis 43 0.031
614
TRN012 Transient Global Amnesia 43 0.031
615
CLL002 Collecting Duct Carcinoma 43 0.031
616
QDR001 Quadriplegia 43 0.031
617
NCR007 Necrotizing Fasciitis 43 0.031
618
P HRN001 Horner's Syndrome 42 0.031
619
GPS001 Gapo Syndrome 42 0.031
620
UTR039 Uterine Fibroid 42 0.031
621
BLR015 Blue Rubber Bleb Nevus Syndrome 41 0.031
622
WRF001 Warfarin Resistance 41 0.031
623
HYP265 Hypotonia 40 0.031
624
CRB085 Cerebral Hemorrhage 40 0.031
625
FCL012 Facial Paralysis 40 0.031
626
LMY003 Leiomyomatosis 39 0.031
627
INT079 Intrahepatic Cholangiocarcinoma 39 0.031
628
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 38 0.031
629
ERY045 Erythrocytosis, Somatic 38 0.031
630
ESN020 Eosinophilic Granulomatosis with Polyangiitis 38 0.031
631
FNT004 Fainting 38 0.031
632
VRL011 Viral Infectious Disease 38 0.031
633
GST053 Gastric Cancer 38 0.031
634
PRS021 Prostatic Adenoma 38 0.031
635
VSC044 Visceral Myopathy 37 0.031
636
MYS004 Myiasis 36 0.031
637
ANG017 Angiolipoma 36 0.031
638
IPX001 Ipex Syndrome 36 0.031
639
c SBC003 Subacute Bacterial Endocarditis 35 0.031
640
CGN006 Cogan Syndrome 35 0.031
641
ADS002 Adie Syndrome 35 0.031
642
MLK004 Malakoplakia 35 0.031
643
P MLD013 Mild Hemophilia a 34 0.031
644
LYM005 Lymphocele 33 0.031
645
HPT012 Hepatocellular Fibrolamellar Carcinoma 33 0.031
646
P PRX010 Paroxysmal Ventricular Fibrillation 33 0.031
647
HPT066 Hepatoportal Sclerosis 32 0.031
648
P ATM020 Autoimmune Enteropathy 30 0.031
649
TYP017 Type 2n Von Willebrand Disease 30 0.031
650
TYP014 Type 2a Von Willebrand Disease 29 0.031
651
TYP016 Type 2m Von Willebrand Disease 29 0.031
652
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 29 0.031
653
NRR001 Neuroretinitis 28 0.031
654
HNM002 Hinman Syndrome 28 0.031
655
WND002 Wandering Spleen 28 0.031
656
TFT003 Tufting Enteropathy 28 0.031
657
PRR008 Periarteritis Nodosa 28 0.031
658
FBR028 Fibrosing Mediastinitis 28 0.031
659
PRM008 Parametritis 27 0.031
660
P FML179 Familial Erythrocytosis 2 26 0.031
661
c ACT036 Acute Cholangitis 25 0.031
662
STR077 Streptococcal Toxic-Shock Syndrome 24 0.031
663
PRF003 Piriformis Syndrome 22 0.031
664
c MLT009 Multiple Cranial Nerve Palsy 21 0.031
665
c ACT035 Acute Frontal Sinusitis 21 0.031
666
SCT001 Sciatic Neuropathy 21 0.031
667
MXD035 Mixed-Type Autoimmune Hemolytic Anemia 21 0.031
668
MSN003 Mesenteric Vascular Occlusion 20 0.031
669
HMC016 Homocystinuria Due to Cbs Deficiency 20 0.031
670
HMC012 Hemicrania Continua 20 0.031
671
MNN005 Meningovascular Neurosyphilis 19 0.031
672
CRD023 Cardiomyopathy Cataract Hip Spine Disease 18 0.031
673
MCR033 Macrocephaly-Capillary Malformation 16 0.031
674
PLM062 Pulmonary Hyalinizing Granuloma 14 0.031
675
CGH002 Cough Headache 14 0.031
676
OCL024 Ocular Neuromyotonia 14 0.031
677
c THR081 Thrombophilia Due to Factor V Leiden 14 0.031
678
SNG003 Single Ventricular Heart 14 0.031
679
CRT056 Carotidynia 13 0.031
680
NNT044 Neonatal Antiphospholipid Syndrome 12 0.031
681
MTH028 Mthfr Thermolabile Variant 10 0.031
682
ACT174 Acute Peripheral Arterial Occlusion 8 0.031
683
c TYP009 Type 2 Diabetes Mellitus 100 0.022
684
P PRK002 Parkinson's Disease 92 0.022
685
P DLT002 Dilated Cardiomyopathy 87 0.022
686
P HMC003 Hemochromatosis 85 0.022
687
FBR012 Fabry Disease 85 0.022
688
P RTT002 Rett Syndrome 83 0.022
689
P CSH001 Cushing's Syndrome 80 0.022
690
P WSK001 Wiskott-Aldrich Syndrome 79 0.022
691
c NNN003 Noonan Syndrome 79 0.022
692
LSC001 Lesch-Nyhan Syndrome 78 0.022
693
ACT033 Acute Intermittent Porphyria 78 0.022
694
SVR004 Severe Combined Immunodeficiency 78 0.022
695
PTZ001 Peutz-Jeghers Syndrome 77 0.022
696
CNG034 Congestive Heart Failure 77 0.022
697
P RBN001 Rubinstein-Taybi Syndrome 77 0.022
698
DCH001 Duchenne Muscular Dystrophy 77 0.022
699
P FRG001 Fragile X Syndrome 77 0.022
700
CRB011 Cerebrotendinous Xanthomatosis 76 0.022
701
P ALP006 Alpha Thalassemia 74 0.022
702
P MLR004 Malaria 74 0.022
703
THY028 Thyroid Cancer 74 0.022
704
P LYM007 Lymphangioleiomyomatosis 74 0.022
705
P SRC013 Sarcoidosis 73 0.022
706
P AMY004 Amyloidosis 73 0.022
707
c OST005 Osteogenesis Imperfecta 72 0.022
708
P PRM006 Primary Biliary Cirrhosis 72 0.022
709
P MYS005 Myositis 71 0.022
710
P RTH001 Rothmund-Thomson Syndrome 70 0.022
711
DNY001 Denys-Drash Syndrome 70 0.022
712
BLL006 Bullous Pemphigoid 69 0.022
713
LKC001 Leukocyte Adhesion Deficiency 69 0.022
714
P STM004 Stomach Cancer 68 0.022
715
ACT010 Acth-Secreting Pituitary Adenoma 68 0.022
716
LMY002 Leiomyoma 67 0.022
717
P HYP117 Hypertriglyceridemia 67 0.022
718
c PRP029 Porphyria 67 0.022
719
P INF038 Influenza 67 0.022
720
MLB002 Male Breast Cancer 67 0.022
721
SPN038 Spina Bifida 66 0.022
722
P ATP001 Atopic Dermatitis 66 0.022
723
ACT049 Acute Disseminated Encephalomyelitis 66 0.022
724
ARG002 Argininosuccinic Aciduria 66 0.022
725
SQM007 Squamous Cell Carcinoma of the Head and Neck 66 0.022
726
MGL001 Megaloblastic Anemia 65 0.022
727
c SPN046 Spinal Muscular Atrophy 65 0.022
728
ARS001 Aarskog-Scott Syndrome 65 0.022
729
P CHR089 Chronic Kidney Failure 65 0.022
730
c UVT001 Uveitis 65 0.022
731
STS003 Sitosterolemia 65 0.022
732
BRN028 Brain Cancer 64 0.022
733
c SCL016 Scleroderma 64 0.022
734
CHL014 Cholera 64 0.022
735
P ALP009 Alopecia Areata 64 0.022
736
MXD005 Mixed Connective Tissue Disease 64 0.022
737
BBS001 Babesiosis 64 0.022
738
KRN002 Kearns-Sayre Syndrome 63 0.022
739
GRY002 Gray Platelet Syndrome 63 0.022
740
P CNG042 Congenital Central Hypoventilation Syndrome 63 0.022
741
P CHN012 Chondrosarcoma 63 0.022
742
P ADL010 Adult Respiratory Distress Syndrome 63 0.022
743
P ART023 Arthropathy 63 0.022
744
HV1006 Hiv-1 63 0.022
745
BLL003 Bell's Palsy 63 0.022
746
c OST026 Osteogenesis Imperfecta Type I 62 0.022
747
CMP002 Campylobacteriosis 62 0.022
748
PSR002 Psoriasis 62 0.022
749
BCK001 Becker Muscular Dystrophy 62 0.022
750
c DST002 Distal Arthrogryposis 62 0.022
751
MLL005 Miller-Dieker Syndrome 62 0.022
752
ACR008 Acrocallosal Syndrome 61 0.022
753
P GTR002 Goiter 61 0.022
754
MLD001 Melioidosis 61 0.022
755
GLC003 Glucose Intolerance 61 0.022
756
JCB001 Jacobsen Syndrome 60 0.022
757
SRS001 Serous Cystadenocarcinoma 60 0.022
758
P RTN025 Retinoschisis 60 0.022
759
P PRM124 Primary Hyperoxaluria Type 1 60 0.022
760
LGN001 Legionnaires' Disease 60 0.022
761
MCS003 Mucous Membrane Pemphigoid 60 0.022
762
BRC012 Brucellosis 60 0.022
763
DST005 Diastrophic Dysplasia 60 0.022
764
HYP003 Hypermethioninemia 60 0.022
765
P BRN009 Burning Mouth Syndrome 59 0.022
766
c DMN001 Diamond-Blackfan Anemia 59 0.022
767
NRN004 Neuroendocrine Tumor 59 0.022
768
DNG003 Dengue Disease 59 0.022
769
CRB021 Cerebral Malaria 59 0.022
770
MYX005 Myxoid Liposarcoma 59 0.022
771
NTH001 Netherton Syndrome 59 0.022
772
MGC001 Megacolon 59 0.022
773
c TRT010 Teratoma 58 0.022
774
ECH003 Echinococcosis 58 0.022
775
AMN001 Amenorrhea 58 0.022
776
CHL068 Cholestasis 58 0.022
777
ISC006 Ischemic Heart Disease 58 0.022
778
BLM002 Bulimia Nervosa 58 0.022
779
c CNG015 Congenital Diaphragmatic Hernia 58 0.022
780
NRN001 Neuroendocrine Carcinoma 58 0.022
781
ANN002 Anencephaly 58 0.022
782
EXT010 Extramedullary Plasmacytoma 58 0.022
783
CRT002 Cartilage-Hair Hypoplasia 57 0.022
784
OBS061 Obstructive Sleep Apnea 57 0.022
785
P DND001 Dandy-Walker Syndrome 57 0.022
786
P SYP003 Syphilis 57 0.022
787
P HRD012 Hereditary Elliptocytosis 57 0.022
788
NRL005 Neurilemmoma 57 0.022
789
c HRD002 Hereditary Angioedema 57 0.022
790
EPT020 Epithelioid Hemangioendothelioma 57 0.022
791
HRP004 Herpes Zoster 57 0.022
792
P SDR002 Siderosis 57 0.022
793
MCN007 Meconium Aspiration Syndrome 56 0.022
794
P ACT009 Acute Monocytic Leukemia 56 0.022
795
c THR003 Thoracic Aortic Aneurysm 56 0.022
796
NTR003 Natural Killer Cell Leukemia 56 0.022
797
ANK001 Ankylosis 56 0.022
798
BRK001 Brooke-Spiegler Syndrome 56 0.022
799
c MNC007 Monocytic Leukemia 56 0.022
800
c PST005 Posterior Uveitis 56 0.022
801
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 56 0.022
802
RNL007 Renal Tubular Acidosis 56 0.022
803
ILT001 Ileitis 56 0.022
804
P PLY006 Polydactyly 56 0.022
805
c MCR010 Microcephaly 56 0.022
806
DBT008 Diabetic Angiopathy 56 0.022
807
CNG048 Congenital Hepatic Fibrosis 56 0.022
808
DNG001 Dengue Shock Syndrome 56 0.022
809
GST037 Gastroparesis 55 0.022
810
c FML035 Familial Hyperlipidemia 55 0.022
811
CLC001 Calciphylaxis 55 0.022
812
ART017 Aortic Disease 55 0.022
813
MTN003 Motion Sickness 55 0.022
814
GST050 Gastrointestinal System Disease 55 0.022
815
LGN002 Legionellosis 55 0.022
816
JPN002 Japanese Encephalitis 55 0.022
817
SPR004 Supravalvular Aortic Stenosis 54 0.022
818
ACT095 Acute Biphenotypic Leukemia 54 0.022
819
MCR004 Macroglobulinemia 54 0.022
820
c HRM001 Hermansky-Pudlak Syndrome 54 0.022
821
IMP005 Impotence 54 0.022
822
FBR003 Fibrous Histiocytoma 54 0.022
823
c DYS142 Dyskeratosis Congenita, Autosomal Recessive 4 54 0.022
824
CYS014 Cystadenocarcinoma 54 0.022
825
MCN001 Mucinous Adenocarcinoma 54 0.022
826
c ADL052 Adult Acute Lymphocytic Leukemia 54 0.022
827
P VNT002 Ventricular Septal Defect 53 0.022
828
STT004 Steatorrhea 53 0.022
829
KLT001 Klatskin's Tumor 53 0.022
830
ORL011 Oral Cancer 53 0.022
831
FML164 Familial Hdl Deficiency 53 0.022
832
P INT072 Intestinal Pseudo-Obstruction 53 0.022
833
P MSC003 Muscular Atrophy 53 0.022
834
PPT005 Peptic Ulcer Disease 53 0.022
835
END020 Endocardial Fibroelastosis 53 0.022
836
HNT002 Hantavirus Pulmonary Syndrome 52 0.022
837
STN007 Stenotrophomonas Maltophilia 52 0.022
838
c RST002 Restrictive Cardiomyopathy 52 0.022
839
c TLN008 Telangiectasia, Hereditary Hemorrhagic, Type 5 52 0.022
840
PRT029 Parathyroid Adenoma 52 0.022
841
c CNT048 Central Hypoventilation Syndrome 52 0.022
842
CLN015 Colon Adenocarcinoma 52 0.022
843
GRW007 Growth Hormone Deficiency 52 0.022
844
ACS001 Acoustic Neuroma 51 0.022
845
IMP002 Imperforate Anus 51 0.022
846
MYC005 Myocardial Stunning 51 0.022
847
P STR020 Strabismus 51 0.022
848
MCL003 Macular Holes 51 0.022
849
SHR001 Short Bowel Syndrome 51 0.022
850
NPH010 Nephrosclerosis 51 0.022
851
PRG008 Paragonimiasis 51 0.022
852
c DRR001 Diarrhea 51 0.022
853
c CMP058 Complex Regional Pain Syndrome Type 1 51 0.022
854
KMR001 Kimura Disease 51 0.022
855
WBR001 Weber Syndrome 50 0.022
856
P CST002 Castleman's Disease 50 0.022
857
LPR001 Lepromatous Leprosy 50 0.022
858
c CRB126 Cerebral Cavernous Malformation 50 0.022
859
RTN001 Retinal Vasculitis 50 0.022
860
c EPS003 Episodic Ataxia 50 0.022
861
CHR288 Chronic Recurrent Multifocal Osteomyelitis 50 0.022
862
ERY017 Erythema Elevatum Diutinum 50 0.022
863
c HYP011 Hyperlipoproteinemia Type Iii 49 0.022
864
PRT026 Parotitis 49 0.022
865
GNT031 Genitopatellar Syndrome 49 0.022
866
DFN221 Deafness Dystonia Syndrome 49 0.022
867
INF058 Inflammatory Myofibroblastic Tumor 49 0.022
868
LFT009 Left Ventricular Outflow Tract Obstruction 49 0.022
869
NNT016 Neonatal Hemochromatosis 49 0.022
870
TLN003 Telangiectasis 49 0.022
871
TRN044 Transposition of the Great Arteries 49 0.022
872
c INT060 Intestinal Atresia 48 0.022
873
DVR002 Diverticulitis 48 0.022
874
c CNT035 Central Nervous System Disease 48 0.022
875
CNV002 Conversion Disorder 48 0.022
876
CRT049 Critical Limb Ischemia 48 0.022
877
P HRD066 Hereditary Angioedema Type Iii 48 0.022
878
PNC033 Pancreas Adenocarcinoma 48 0.022
879
c ACT150 Acute Adrenal Insufficiency 48 0.022
880
PLM010 Pulmonary Edema 48 0.022
881
CRN027 Corneal Neovascularization 47 0.022
882
QBC001 Quebec Platelet Disorder 47 0.022
883
BRN014 Bronchopneumonia 47 0.022
884
GLM037 Glioma Somatic 47 0.022
885
NNT020 Neonatal Intrahepatic Cholestasis Caused by Citrin Deficiency 47 0.022
886
PRN021 Paranasal Sinus Disease 47 0.022
887
CRT008 Carotid Artery Dissection 47 0.022
888
MNC006 Monoclonal Gammopathy of Uncertain Significance 47 0.022
889
c MLG086 Malignant Hyperthermia Susceptibility 46 0.022
890
P TRN034 Transverse Myelitis 46 0.022
891
MYS001 Myositis Ossificans 46 0.022
892
HYP054 Hypochromic Anemia 46 0.022
893
SML026 Small Fiber Neuropathy 46 0.022
894
TBR008 Tuberculous Peritonitis 46 0.022
895
MNN009 Meningoencephalitis 46 0.022
896
P CRB088 Cerebral Atrophy 46 0.022
897
SCR024 Sacrococcygeal Teratoma 46 0.022
898
P HMR003 Hemorrhagic Disease 45 0.022
899
MNN017 Mononeuropathy 45 0.022
900
BWN003 Bowenoid Papulosis 45 0.022
901
PLM052 Pulmonary Arteriovenous Malformation 45 0.022
902
WLL004 Wallerian Degeneration 45 0.022
903
ART004 Aortic Atherosclerosis 45 0.022
904
P NRL007 Neurologic Diseases 45 0.022
905
INF034 Infective Endocarditis 44 0.022
906
HRS011 Horseshoe Kidney 44 0.022
907
c JVN024 Juvenile Hereditary Hemochromatosis 44 0.022
908
LYM011 Lymphogranuloma Venereum 44 0.022
909
UTR024 Uterine Carcinosarcoma 44 0.022
910
P ADM005 Adams-Oliver Syndrome 1 44 0.022
911
FTT001 Fatty Liver Disease 44 0.022
912
SYN036 Syncope 44 0.022
913
PLC005 Placental Insufficiency 43 0.022
914
CHN015 Chondrodysplasia 43 0.022
915
c APH002 Aphasia 43 0.022
916
RTC005 Reticulosarcoma 43 0.022
917
CHR010 Chorioangioma 43 0.022
918
HPT022 Hepatoblastoma 43 0.022
919
c CHR342 Chiari Malformation 43 0.022
920
CRB004 Cerebral Artery Occlusion 43 0.022
921
ADN027 Adenomyosis 43 0.022
922
CRN030 Coronary Stenosis 43 0.022
923
PLR005 Pleuropneumonia 43 0.022
924
DFC001 Defective Apolipoprotein B-100 42 0.022
925
LMB052 Lumbar Disc Herniation 42 0.022
926
MCK002 Meckel's Diverticulum 42 0.022
927
P THR045 Thrombotic Thrombocytopenic Purpura, Congenital 42 0.022
928
INT071 Intestinal Perforation 42 0.022
929
ESP002 Esophageal Varix 41 0.022
930
GLY015 Glycine N-Methyltransferase Deficiency 41 0.022
931
P VGN017 Vaginal Cancer 41 0.022
932
GST071 Gastrointestinal Carcinoma 41 0.022
933
CRD016 Cardiac Rupture 41 0.022
934
XNT001 Xanthogranulomatous Pyelonephritis 41 0.022
935
P BRN035 Brain Stem Glioma 41 0.022
936
HMT018 Hematopoietic Stem Cell Transplantation 40 0.022
937
GST040 Gastric Adenocarcinoma 40 0.022
938
P DPH016 Diaphragmatic Hernia 3 40 0.022
939
P MNN007 Meningocele 40 0.022
940
WTH001 Withdrawal Disorder 40 0.022
941
RBF001 Riboflavin Deficiency 40 0.022
942
ACL001 Acalculous Cholecystitis 40 0.022
943
STR037 Stress Cardiomyopathy 40 0.022
944
HMP018 Hemophilic Arthropathy 40 0.022
945
INP001 Inappropriate Adh Syndrome 40 0.022
946
SCT002 Scotoma 40 0.022
947
KDN015 Kidney Angiomyolipoma 39 0.022
948
LNS001 Lens Subluxation 39 0.022
949
c TYP002 Type Vi Ehlers-Danlos Syndrome 39 0.022
950
VTM001 Vitamin K Deficiency Hemorrhagic Disease 39 0.022
951
ART012 Aortitis 39 0.022
952
P HYP071 Hypersensitivity Reaction Type Ii Disease 39 0.022
953
TBR006 Tuberculoid Leprosy 39 0.022
954
ALC005 Alcoholic Pancreatitis 39 0.022
955
HYP143 Hypomyelination and Congenital Cataract 39 0.022
956
P CHR038 Chronic Maxillary Sinusitis 38 0.022
957
GLY032 Glycosylphosphatidylinositol Deficiency 38 0.022
958
PRT086 Partial Hydatidiform Mole 38 0.022
959
SGN002 Signet Ring Cell Adenocarcinoma 38 0.022
960
CHL061 Childhood Leukemia 38 0.022
961
CMB021 Combined Pituitary Hormone Deficiency 38 0.022
962
SPR066 Superficial Siderosis 38 0.022
963
P SYS007 Systemic Capillary Leak Syndrome 38 0.022
964
c CNG071 Congenital Disorder of Glycosylation Type 1b 38 0.022
965
PTT021 Pituitary Hormone Deficiency, Combined 2 37 0.022
966
ADN002 Adenoiditis 37 0.022
967
DXT002 Dextrocardia with Situs Inversus 37 0.022
968
c FML162 Familial Mediterranean Fever, Ad 37 0.022
969
BRN055 Bronchogenic Cyst 37 0.022
970
CTR003 Citrin Deficiency 37 0.022
971
FTD001 Foot Drop 36 0.022
972
PRL008 Paralytic Ileus 36 0.022
973
HMG020 Hmg Coa Lyase Deficiency 36 0.022
974
CNG069 Congenital Cytomegalovirus 36 0.022
975
OPT006 Optic Nerve Disease 35 0.022
976
P CHR454 Chiari Malformation Type 1 35 0.022
977
RHS001 Rh Isoimmunization 34 0.022
978
CNG219 Congenital Aural Atresia 34 0.022
979
FTL012 Fetal and Neonatal Alloimmune Thrombocytopenia 34 0.022
980
INT042 Internuclear Ophthalmoplegia 34 0.022
981
SPR007 Superior Mesenteric Artery Syndrome 34 0.022
982
c ACQ010 Acquired Polycythemia 34 0.022
983
PLY024 Polymicrogyria 33 0.022
984
ANG049 Angioedema Induced by Ace Inhibitors 33 0.022
985
NTR005 Nutritional Deficiency Disease 33 0.022
986
c SVR057 Severe Hemophilia B 32 0.022
987
CRN185 Craniofacial Deafness Hand Syndrome 32 0.022
988
ULN001 Ulnar Neuropathy 31 0.022
989
MGL023 Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome, Somatic 31 0.022
990
TST021 Testicular Germ Cell Tumor 31 0.022
991
P 49X002 49,xxxxy Syndrome 31 0.022
992
HMX002 Heme Oxygenase-1 Deficiency 31 0.022
993
SPL007 Splenic Abscess 30 0.022
994
ADT003 Auditory System Disease 30 0.022
995
PNG002 Pain Agnosia 30 0.022
996
NRC019 Neurocutaneous Melanosis, Somatic 30 0.022
997
CNG134 Congenitally Corrected Transposition of the Great Arteries 30 0.022
998
P CMM008 Communicating Hydrocephalus 30 0.022
999
PRN037 Prinzmetal's Variant Angina 29 0.022
1000
TXC001 Toxic Megacolon 29 0.022
1001
SBC014 Subclavian Steal Syndrome 29 0.022
1002
CRT045 Creatine Phosphokinase, Elevated Serum 28 0.022
1003
MLN013 Melanoma Metastasis 28 0.022
1004
DYS003 Dysgraphia 28 0.022
1005
P DCR004 Dacryocystitis 28 0.022
1006
BLD052 Blood Group Incompatibility 27 0.022
1007
SPR032 Superficial Siderosis of the Central Nervous System 27 0.022
1008
GNT005 Giant Hemangioma 27 0.022
1009
CRN019 Coronary Artery Vasospasm 27 0.022
1010
RHB020 Rhabdomyosarcoma, Somatic 27 0.022
1011
MCR216 Microcephaly with or Without Chorioretinopathy, Lymphedema, or Mental Retardation 26 0.022
1012
CRT028 Cor Triatriatum 26 0.022
1013
CPL011 Capillary Malformations, Congenital, 1, Somatic, Mosaic 26 0.022
1014
ANT013 Anterior Spinal Artery Syndrome 26 0.022
1015
P CHR097 Chronic Purulent Otitis Media 25 0.022
1016
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 25 0.022
1017
c MLD014 Mild Hemophilia B 25 0.022
1018
ABD002 Abducens Nerve Disease 25 0.022
1019
CHR034 Chromophobe Adenoma 25 0.022
1020
HMR039 Hemorrhage, Intracerebral 24 0.022
1021
PRN007 Perinephritis 24 0.022
1022
ANG022 Angel Shaped Phalangoepiphyseal Dysplasia 24 0.022
1023
EMB002 Embryoma 24 0.022
1024
STR080 Stroke, Hemorrhagic 23 0.022
1025
MSN002 Mesenteric Lymphadenitis 23 0.022
1026
SBS002 Substernal Goiter 22 0.022
1027
c CNG379 Congenital Disorder of Glycosylation, Type It 22 0.022
1028
c PST001 Posterior Myocardial Infarction 22 0.022
1029
MNG003 Mungan Syndrome 22 0.022
1030
INT147 Intrauterine Growth Restriction, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 22 0.022
1031
MYX006 Myxoid Leiomyosarcoma 22 0.022
1032
VRT001 Vertebral Artery Occlusion 22 0.022
1033
MLT037 Multifocal Lymphangioendotheliomatosis with Thrombocytopenia 22 0.022
1034
PLY004 Polyp of Corpus Uteri 21 0.022
1035
ACT201 Acute Posterior Multifocal Placoid Pigment Epitheliopathy 21 0.022
1036
CNG171 Congenital Plasminogen Deficiency 21 0.022
1037
RHM007 Rheumatic Congestive Heart Failure 21 0.022
1038
PRP021 Peripheral Nervous System Neoplasm 21 0.022
1039
SBC002 Subclavian Artery Aneurysm 20 0.022
1040
P HMN004 Hemangioma of Liver 20 0.022
1041
P OCL041 Oculomotor Apraxia Cogan Type 20 0.022
1042
QLT001 Qualitative Platelet Defect 20 0.022
1043
RCT009 Rectosigmoid Cancer 19 0.022
1044
MDN008 Median Arcuate Ligament Syndrome 19 0.022
1045
PLS001 Pulsating Exophthalmos 19 0.022
1046
HYP015 Hyperlucent Lung 19 0.022
1047
BNT001 Banti's Syndrome 18 0.022
1048
FRN014 Fournier Gangrene 18 0.022
1049
ART109 Arterial Thoracic Outlet Syndrome 18 0.022
1050
FXL001 Foix-Alajouanine Syndrome 18 0.022
1051
PNT023 Pontine Hemorrhage 18 0.022
1052
CHR076 Choriocarcinoma of the Testis 18 0.022
1053
INT010 Intracranial Embolism 18 0.022
1054
CNT067 Central Cord Syndrome 18 0.022
1055
OTP003 Oto-Palatal-Digital Syndrome 17 0.022
1056
MGL021 Megalencephaly-Capillary Malformation Syndrome 17 0.022
1057
48X002 48,xxxy Syndrome 17 0.022
1058
CNG298 Congenital Pancreatic Cyst 17 0.022
1059
RNL001 Renal Artery Obstruction 17 0.022
1060
CNG092 Congenital Extrahepatic Portosystemic Shunt 16 0.022
1061
XLN139 X-Linked Intellectual Disability - Macrocephaly - Macroorchidism 16 0.022
1062
TMP006 Temporomandibular Ankylosis 16 0.022
1063
THR021 Thrombophilia Due to Hrg Deficiency 15 0.022
1064
THR068 Thrombophilia Due to Protein C Deficiency, Autosomal Recessive 15 0.022
1065
DRL001 Dural Sinus Malformation 14 0.022
1066
GST016 Gastric Signet Ring Cell Adenocarcinoma 14 0.022
1067
BLT017 Bilateral Massive Adrenal Hemorrhage 14 0.022
1068
CVR001 Cavernous Sinus Meningioma 13 0.022
1069
c EHL052 Ehlers-Danlos Syndrome, Vascular Type 13 0.022
1070
THR020 Thrombophilia Due to Heparin Cofactor Ii Deficiency 12 0.022
1071
CYS035 Cystic Adventitial Disease 12 0.022
1072
INF001 Infarct of Liver 12 0.022
1073
INT055 Intravascular Fasciitis 10 0.022
1074
c THR060 Thrombophilia, Familial, Due to Decreased Release of Plat 10 0.022
1075
THR055 Thrombophilia, X-Linked, Due to Factor Ix Defect 8 0.022
1076
c PRT053 Portal Hypertension Due to Infrahepatic Block 4 0.022