Search results for "thrombosis"

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

1065 hits were found for 'thrombosis'

# Family MCID Name MIFTS Score
1
SGT001 Sagittal Sinus Thrombosis 50 6.156
2
PRT018 Portal Vein Thrombosis 55 5.346
3
CRN017 Coronary Thrombosis 60 5.283
4
LTR002 Lateral Sinus Thrombosis 25 5.159
5
VNS009 Venous Thrombosis 60 5.129
6
INT078 Intracranial Thrombosis 32 4.776
7
CVR002 Cavernous Sinus Thrombosis 27 4.565
8
CRT004 Carotid Artery Thrombosis 47 3.979
9
HPT002 Hepatic Vein Thrombosis 66 3.897
10
INT076 Intracranial Sinus Thrombosis 15 3.162
11
CRB132 Cerebral Sinovenous Thrombosis 42 2.871
12
VNS011 Venous Thrombosis, Protection Against 18 2.556
13
WRF005 Warfarine Dose Selection in the Treatment of Venous Thrombosis and Atrial Fibrillation 13 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 3 2.530
18
RSS010 Resistance to Warfarine in Venous Thrombosis and Atrial Fibrillation 3 2.530
19
RSS015 Resistance to Phenprocoumon in Venous Thrombosis and Atrial Fibrillation 3 2.530
20
RSS018 Resistance to Fluindione in Venous Thrombosis and Atrial Fibrillation 3 2.530
21
MND006 Mondor Disease 19 1.822
22
VNS012 Venous Thoracic Outlet Syndrome 19 1.789
23
CRB009 Cerebritis 39 0.510
24
c HPT021 Hepatitis 64 0.272
25
PRT014 Protein S Deficiency 65 0.267
26
P THR015 Thrombophilia 67 0.262
27
P MYC007 Myocardial Infarction 93 0.261
28
PLM033 Pulmonary Embolism 66 0.244
29
c THR014 Thrombocytopenia 71 0.241
30
HPR003 Heparin-Induced Thrombocytopenia 53 0.236
31
PRT011 Protein C Deficiency 56 0.231
32
ANT006 Antiphospholipid Syndrome 66 0.228
33
P HYP075 Hypertension 87 0.198
34
ANR040 Aneurysm 46 0.196
35
THR079 Thromboembolism 66 0.181
36
HPT023 Hepatocellular Carcinoma 54 0.181
37
P SYS001 Systemic Lupus Erythematosus 88 0.177
38
ANT009 Antithrombin Iii Deficiency 59 0.177
39
c LPS004 Lupus Erythematosus 77 0.176
40
HYP037 Hyperhomocysteinemia 53 0.174
41
END072 Endotheliitis 51 0.170
42
c ESS003 Essential Thrombocythemia 61 0.165
43
c NPH012 Nephrotic Syndrome 67 0.159
44
c ACT075 Acute Myocardial Infarction 60 0.146
45
P LKM002 Leukemia 77 0.144
46
c PNC044 Pancreatitis 69 0.141
47
CLT003 Colitis 64 0.139
48
VNS010 Venous Thromboembolism 55 0.139
49
THR016 Thrombophlebitis 69 0.137
50
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 54 0.136
51
HMG002 Hemoglobinuria 52 0.136
52
PLY001 Polycythemia Vera 85 0.134
53
ULC004 Ulcerative Colitis 65 0.134
54
c PLY018 Polycythemia 59 0.134
55
HDC001 Headache 58 0.130
56
P PRT013 Portal Hypertension 66 0.128
57
ART111 Artery Disease 62 0.126
58
LVR012 Liver Cirrhosis 77 0.124
59
ATH003 Atherosclerosis 69 0.124
60
P SNS014 Sinusitis 58 0.122
61
DSS009 Disseminated Intravascular Coagulation 62 0.116
62
RTN023 Retinitis 54 0.116
63
c MNN013 Meningitis 68 0.114
64
THR004 Thrombocytosis 61 0.111
65
c INF037 Inflammatory Bowel Disease 40 0.111
66
PRP030 Purpura 66 0.109
67
INT003 Intracranial Hypotension 30 0.109
68
DYS026 Dysfibrinogenemia 63 0.107
69
CLL003 Cellulitis 59 0.107
70
P HYP098 Hypereosinophilic Syndrome 62 0.105
71
OTT002 Otitis Media 58 0.105
72
HDN002 Head Injury 49 0.105
73
THR013 Thoracic Outlet Syndrome 52 0.102
74
P ART084 Arteriovenous Fistula 47 0.102
75
ISC004 Ischemia 63 0.100
76
P HMC002 Homocystinuria 60 0.100
77
OVR029 Ovarian Hyperstimulation Syndrome 67 0.097
78
FCT004 Factor Xii Deficiency 66 0.095
79
INT075 Intracranial Hypertension 53 0.095
80
PST095 Post-Thrombotic Syndrome 42 0.095
81
PSD002 Pseudotumor Cerebri 55 0.092
82
BLN003 Blindness 53 0.092
83
TBR010 Tuberculosis 87 0.086
84
P OBS005 Obesity 91 0.083
85
c ACT027 Acute Pancreatitis 64 0.083
86
PRG060 Pregnancy Loss 48 0.083
87
THR006 Thromboangiitis Obliterans 79 0.080
88
FCT007 Factor Vii Deficiency 79 0.080
89
CRH001 Crohn's Disease 76 0.080
90
c DBT009 Diabetes Mellitus 74 0.080
91
c PLM037 Pulmonary Hypertension 73 0.080
92
c HMP007 Hemophilia 65 0.080
93
DFC004 Deficiency Anemia 63 0.080
94
MYM001 Myoma 56 0.080
95
PPL021 Papilledema 54 0.080
96
CTS005 Catastrophic Antiphospholipid Syndrome 52 0.080
97
CRD137 Cardiogenic Shock 49 0.080
98
SPR035 Superior Vena Cava Syndrome 40 0.080
99
CRB039 Cerebrovascular Disease 69 0.077
100
ACT119 Acute Promyelocytic Leukemia 68 0.077
101
IRN001 Iron Deficiency Anemia 57 0.077
102
CRN006 Coronary Aneurysm 49 0.077
103
CYT008 Cytomegalovirus Infection 44 0.077
104
SPL006 Splenic Infarction 39 0.077
105
LMR001 Lemierre's Syndrome 32 0.077
106
ORB006 Orbital Cellulitis 30 0.077
107
P MYL005 Myelofibrosis 75 0.074
108
VSC007 Vascular Disease 70 0.074
109
STR067 Stroke, Ischemic 65 0.074
110
PTN001 Patent Foramen Ovale 62 0.074
111
P ADN016 Adenocarcinoma 59 0.074
112
P RTN022 Retinal Vein Occlusion 57 0.074
113
c OST028 Osteochondroma 54 0.074
114
SYN053 Syndromic Diarrhea 34 0.074
115
BHC002 Behcet's Disease 79 0.070
116
ANK002 Ankylosing Spondylitis 77 0.070
117
P ANG001 Angelman Syndrome 70 0.070
118
P GLM007 Glomerulonephritis 69 0.070
119
P HYD006 Hydrocephalus 68 0.070
120
ART019 Aortic Valve Stenosis 64 0.070
121
P RNL014 Renal Cell Carcinoma 64 0.070
122
ACN002 Acanthosis Nigricans 63 0.070
123
P ACT101 Acute Lymphoblastic Leukemia 63 0.070
124
c AFB001 Afibrinogenemia 62 0.070
125
P CRV039 Cervicitis 58 0.070
126
c CNT016 Central Retinal Vein Occlusion 58 0.070
127
c RTN014 Retinal Artery Occlusion 58 0.070
128
c LYM026 Lymphoblastic Leukemia 57 0.070
129
P HYP083 Hypopituitarism 53 0.070
130
MMB002 Membranous Glomerulonephritis 53 0.070
131
P ATX010 Ataxia Neuropathy Spectrum 43 0.070
132
P LVR011 Liver Cancer 91 0.067
133
PRT036 Peritonitis 72 0.067
134
VNW001 Von Willebrand's Disease 72 0.067
135
SPS077 Sepsis 70 0.067
136
THY033 Thyrotoxicosis 58 0.067
137
HLL004 Hellp Syndrome 54 0.067
138
HMC014 Homocysteinemia 49 0.067
139
CHY006 Chylous Ascites 48 0.067
140
THR035 Thrombasthenia 45 0.067
141
CRT015 Carotid Artery Occlusion 45 0.067
142
VRC005 Varicose Veins 45 0.067
143
SPN185 Spinal Cord Infarction 43 0.067
144
P BRS047 Breast Cancer 86 0.063
145
CDS001 Cadasil 84 0.063
146
P PRC016 Pre-Eclampsia 78 0.063
147
P HMP004 Hemophilia B 78 0.063
148
KWS002 Kawasaki Disease 76 0.063
149
P ART022 Arthritis 75 0.063
150
c THL005 Thalassemia 72 0.063
151
ART016 Aortic Aneurysm 71 0.063
152
SRC014 Sarcoma 70 0.063
153
P LVR013 Liver Disease 69 0.063
154
P HRD011 Hereditary Spherocytosis 67 0.063
155
VSC011 Vasculitis 66 0.063
156
FCT002 Factor Xi Deficiency 65 0.063
157
c ECL001 Eclampsia 64 0.063
158
FCT006 Factor V Deficiency 64 0.063
159
c HYP076 Hyperthyroidism 64 0.063
160
ART005 Arteriovenous Malformation 63 0.063
161
SCK005 Sickle Cell Disease 62 0.063
162
SND002 Sneddon Syndrome 60 0.063
163
P END033 Endocarditis 57 0.063
164
c ISC002 Ischemic Optic Neuropathy 57 0.063
165
P INT030 Intracranial Aneurysm 56 0.063
166
P CNT028 Central Retinal Artery Occlusion 53 0.063
167
ISC015 Ischemic Colitis 52 0.063
168
NNT024 Neonatal Stroke 51 0.063
169
ANG054 Angina Pectoris 47 0.063
170
EVN001 Evans' Syndrome 46 0.063
171
BRS090 Breast Reconstruction 44 0.063
172
BRN026 Branch Retinal Artery Occlusion 44 0.063
173
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 42 0.063
174
P CRN074 Coronary Artery Aneurysm 40 0.063
175
FCT013 Factor V Leiden Thrombophilia 34 0.063
176
SPH007 Sphenoid Sinusitis 26 0.063
177
MYT019 May–thurner Syndrome 14 0.063
178
P ATX002 Ataxia Telangiectasia 87 0.059
179
P APL001 Aplastic Anemia 83 0.059
180
MYL040 Myelodysplastic Syndromes 81 0.059
181
c MYL006 Myeloid Leukemia 75 0.059
182
P HPT001 Hepatitis C 67 0.059
183
LGG001 Legg-Calve-Perthes Disease 66 0.059
184
P ESN007 Eosinophilia 63 0.059
185
NRP001 Neuropathy 62 0.059
186
CHL067 Cholecystitis 61 0.059
187
SPH001 Sapho Syndrome 60 0.059
188
P ANT058 Anterior Ischemic Optic Neuropathy 59 0.059
189
P THR090 Thrombocythemia 1 58 0.059
190
c ACT073 Acute Leukemia 57 0.059
191
ART001 Arterial Tortuosity Syndrome 55 0.059
192
AND003 Andersen-Tawil Syndrome 54 0.059
193
BCT015 Bacteremia 50 0.059
194
BRN106 Burns 50 0.059
195
MNN021 Meningococcemia 48 0.059
196
P VNS003 Venous Insufficiency 48 0.059
197
CHR466 Chronic Thromboembolic Pulmonary Hypertension 43 0.059
198
SPP008 Suppurative Otitis Media 42 0.059
199
c ACQ012 Acquired Angioedema 42 0.059
200
PRP028 Peripheral Vertigo 41 0.059
201
PTR001 Petrositis 29 0.059
202
P LPR003 Leprosy 78 0.055
203
P PNM007 Pneumonia 78 0.055
204
GLN003 Glanzmann's Thrombasthenia 74 0.055
205
c HYP095 Hypercholesterolemia 73 0.055
206
RLP001 Relapsing Polychondritis 72 0.055
207
c HPT016 Hepatitis B 70 0.055
208
ART021 Arteriosclerosis 68 0.055
209
P ABD003 Abdominal Aortic Aneurysm 68 0.055
210
DBT001 Diabetic Ketoacidosis 66 0.055
211
FCT003 Factor X Deficiency 64 0.055
212
BLR001 Biliary Atresia 63 0.055
213
SPN186 Spinal Cord Injury 62 0.055
214
SPT013 Septic Shock 61 0.055
215
PRP007 Priapism 60 0.055
216
c THR005 Thrombotic Thrombocytopenic Purpura 59 0.055
217
HYP063 Hypersplenism 59 0.055
218
P CNG019 Congenital Afibrinogenemia 57 0.055
219
HPT019 Hepatic Encephalopathy 57 0.055
220
P CMP008 Compartment Syndrome 56 0.055
221
TYP013 Type 1 Von Willebrand Disease 55 0.055
222
c ACR001 Aicardi-Goutieres Syndrome 54 0.055
223
c ACQ014 Acquired Hemophilia 52 0.055
224
MNT147 Mental Retardation 52 0.055
225
PRT019 Protein-Losing Enteropathy 51 0.055
226
MLK003 Melkersson-Rosenthal Syndrome 51 0.055
227
FCT005 Factor Xiii Deficiency 50 0.055
228
ACT099 Acute Fatty Liver of Pregnancy 50 0.055
229
ERY004 Erysipelas 50 0.055
230
RTR011 Retroperitoneal Fibrosis 48 0.055
231
ABD004 Abdominal Tuberculosis 47 0.055
232
MDS022 Mediastinitis 46 0.055
233
VND001 Vein Disease 44 0.055
234
BLD054 Blood Protein Disease 38 0.055
235
INF133 Inferior Vena Cava Interruption 35 0.055
236
HMC004 Homocysteine Plasma Level 33 0.055
237
MTH044 Mthfr Gene Mutation 33 0.055
238
PRX023 Paroxysmal Nocturnal Hemoglobinuria, Somatic 32 0.055
239
c FRN011 Frontal Sinusitis 30 0.055
240
SBD001 Subdural Empyema 27 0.055
241
c BNG076 Benign Exophthalmos Syndrome 22 0.055
242
HRD083 Hereditary Antithrombin Deficiency 22 0.055
243
HGH021 Hughes-Stovin Syndrome 21 0.055
244
HDG007 Hodgkin's Lymphoma 93 0.050
245
SCK003 Sickle Cell Anemia 82 0.050
246
AND002 Androgen Insensitivity Syndrome 80 0.050
247
P PHC003 Pheochromocytoma 80 0.050
248
P LNG032 Lung Cancer 79 0.050
249
BRK003 Burkitt's Lymphoma 77 0.050
250
P FML018 Familial Mediterranean Fever 76 0.050
251
ASP006 Aspergillosis 73 0.050
252
FCT001 Factor Viii Deficiency 73 0.050
253
ACQ007 Acquired Immunodeficiency Syndrome 71 0.050
254
P CNG401 Congenital Heart Disease 69 0.050
255
c AXN002 Axenfeld-Rieger Syndrome 67 0.050
256
GST009 Gastroschisis 66 0.050
257
c HML002 Hemolytic Anemia 66 0.050
258
P BRN019 Bernard-Soulier Syndrome 65 0.050
259
P CLN016 Colon Cancer 65 0.050
260
c INT070 Intestinal Obstruction 63 0.050
261
P LMY004 Leiomyosarcoma 62 0.050
262
c MYL007 Myeloma 61 0.050
263
ADR015 Adrenocortical Carcinoma 61 0.050
264
PRS047 Prostatitis 60 0.050
265
MYC002 Mycobacterium Avium Complex Disease 59 0.050
266
ANR004 Anuria 59 0.050
267
OST017 Osteomyelitis 59 0.050
268
CHR001 Churg-Strauss Syndrome 58 0.050
269
NDL013 Nodular Regenerative Hyperplasia 57 0.050
270
DDN006 Duodenitis 56 0.050
271
APP008 Appendicitis 56 0.050
272
KLN001 Klinefelter's Syndrome 56 0.050
273
MYL001 Myelitis 55 0.050
274
P PYL005 Pyelonephritis 55 0.050
275
CHL069 Cholesteatoma 55 0.050
276
NPH051 Nephritis 54 0.050
277
EXS001 Exostosis 52 0.050
278
c SVR056 Severe Hemophilia a 50 0.050
279
NNR007 Non-Arteritic Anterior Ischemic Optic Neuropathy 50 0.050
280
FSC004 Fasciitis 46 0.050
281
ART110 Arteritic Anterior Ischemic Optic Neuropathy 45 0.050
282
ZYG002 Zygomycosis 45 0.050
283
CRT012 Cortical Blindness 44 0.050
284
CDQ001 Cauda Equina Syndrome 42 0.050
285
AMR003 Amaurosis Fugax 41 0.050
286
LCK001 Locked-in Syndrome 41 0.050
287
PRP080 Peripheral Artery Disease 36 0.050
288
AND005 Androgen Insensitivity Syndrome, Mild 21 0.050
289
HMC030 Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency 19 0.050
290
ORB016 Orbital Varix 14 0.050
291
c THR023 Thrombophilia Due to Thrombomodulin Defect 9 0.050
292
P FML021 Familial Hypercholesterolemia 86 0.045
293
P MLT020 Multiple Sclerosis 85 0.045
294
c BTT002 Beta Thalassemia 78 0.045
295
TTR001 Tetralogy of Fallot 75 0.045
296
P WGN002 Wegener's Granulomatosis 74 0.045
297
c CHR065 Chronic Myeloid Leukemia 73 0.045
298
P TMP003 Temporal Arteritis 72 0.045
299
SCH014 Schistosomiasis 72 0.045
300
c ACT074 Acute Lymphocytic Leukemia 70 0.045
301
MRB003 Morbid Obesity 68 0.045
302
P ESP024 Esophagitis 64 0.045
303
CRN036 Craniopharyngioma 63 0.045
304
c KDN018 Kidney Disease 63 0.045
305
TYP007 Typhoid Fever 62 0.045
306
P ATM010 Autoimmune Hemolytic Anemia 62 0.045
307
CHR074 Choriocarcinoma 61 0.045
308
P SCH018 Schizencephaly 61 0.045
309
P END047 Endophthalmitis 60 0.045
310
c SLP006 Sleep Apnea 59 0.045
311
URM002 Uremia 58 0.045
312
P HMR012 Hemorrhagic Fever 58 0.045
313
INT007 Intermediate Coronary Syndrome 57 0.045
314
RDC002 Radiculopathy 56 0.045
315
PNM013 Pneumococcal Meningitis 56 0.045
316
CRD001 Cardiac Tamponade 55 0.045
317
INT002 Intermittent Claudication 55 0.045
318
ANG011 Angiodysplasia 55 0.045
319
c ACT134 Acute Liver Failure 54 0.045
320
SPT004 Septic Arthritis 53 0.045
321
LPS007 Lupus Nephritis 53 0.045
322
PRC013 Pericarditis 53 0.045
323
HMR002 Hemarthrosis 52 0.045
324
ANG018 Angiomyolipoma 52 0.045
325
P PND001 Pain Disorder 52 0.045
326
VRC001 Varicocele 51 0.045
327
CRN020 Coronary Restenosis 51 0.045
328
P GRV001 Graves' Disease 51 0.045
329
CCN002 Cocaine Abuse 51 0.045
330
c ERY013 Erythrocytosis 50 0.045
331
OPT009 Optic Neuritis 50 0.045
332
NRT004 Neuritis 49 0.045
333
SPN035 Spindle Cell Sarcoma 49 0.045
334
CHL004 Cholelithiasis 48 0.045
335
MYC020 Mycobacterium Tuberculosis, Susceptibility to Infection by 48 0.045
336
VTM002 Vitamin B12 Deficiency 48 0.045
337
LYM021 Lymphadenitis 48 0.045
338
c PRN026 Porencephaly 48 0.045
339
ACT055 Actinomycosis 47 0.045
340
ACQ017 Acquired Von Willebrand Syndrome 47 0.045
341
ESN011 Eisenmenger Syndrome 45 0.045
342
NRN002 Neuronitis 44 0.045
343
NPH017 Nephrosis 42 0.045
344
c CHR431 Chronic Venous Insufficiency 39 0.045
345
SCR015 Scarlet Fever 37 0.045
346
HMR001 Hemorrhagic Thrombocythemia 35 0.045
347
IMM088 Immunodeficiency 36 34 0.045
348
PRT045 Prothrombin-Related Thrombophilia 31 0.045
349
CNG058 Congenital Antithrombin Deficiency Type 3 31 0.045
350
VNF001 Vein of Galen Aneurysm 30 0.045
351
IRN002 Iron Metabolism Disease 28 0.045
352
SHW001 Shwartzman Phenomenon 25 0.045
353
THN005 Thunderclap Headache 19 0.045
354
DBL009 Double Inferior Vena Cava 18 0.045
355
c ACT061 Acute Sphenoidal Sinusitis 17 0.045
356
CYS001 Cystic Fibrosis 97 0.039
357
P RHM011 Rheumatoid Arthritis 94 0.039
358
P ACT019 Acute Myeloid Leukemia 93 0.039
359
P CHR090 Chronic Lymphocytic Leukemia 89 0.039
360
P MLT019 Multiple Myeloma 88 0.039
361
P OVR042 Ovarian Cancer 85 0.039
362
P PRM021 Primary Pulmonary Hypertension 77 0.039
363
P AST007 Astrocytoma 74 0.039
364
P CLC005 Celiac Disease 73 0.039
365
KLP002 Klippel-Trenaunay Syndrome 69 0.039
366
GSG001 Gas Gangrene 68 0.039
367
PRP027 Peripheral Vascular Disease 68 0.039
368
P TRN020 Turner Syndrome 67 0.039
369
c THY032 Thyroiditis 66 0.039
370
PHR003 Pharyngitis 66 0.039
371
DRM006 Dermatitis 66 0.039
372
c ENC004 Encephalitis 66 0.039
373
P MLN008 Melanoma 65 0.039
374
c VRL010 Viral Hepatitis 64 0.039
375
c MLG069 Malignant Hypertension 64 0.039
376
VGN023 Vaginitis 63 0.039
377
P MTR012 Mitral Valve Disease 63 0.039
378
HYP066 Hyperglycemia 62 0.039
379
P CNJ013 Conjunctivitis 62 0.039
380
P RNV001 Renovascular Hypertension 62 0.039
381
HYD012 Hydrops Fetalis 62 0.039
382
c ALM001 Al Amyloidosis 61 0.039
383
P LPS002 Liposarcoma 60 0.039
384
CHC001 Chickenpox 60 0.039
385
CRY004 Cryoglobulinemia 59 0.039
386
LYM019 Lymphosarcoma 59 0.039
387
PLY041 Polymyositis 59 0.039
388
P MYM002 Moyamoya Disease 58 0.039
389
BRN029 Brain Disease 58 0.039
390
PRT039 Proteinuria 58 0.039
391
BRN071 Brain Injury 58 0.039
392
P BCL006 B-Cell Lymphomas 57 0.039
393
OCL006 Ocular Hypertension 55 0.039
394
P EXP004 Exophthalmos 55 0.039
395
HST009 Histiocytoma 55 0.039
396
NPH011 Nephroblastoma 55 0.039
397
EBS001 Ebstein Anomaly 55 0.039
398
BNM001 Bone Marrow Cancer 54 0.039
399
TRM010 Traumatic Brain Injury 54 0.039
400
PRN011 Pernicious Anemia 53 0.039
401
c OPH004 Ophthalmoplegia 53 0.039
402
c LYM025 Lymphedema 53 0.039
403
INT221 Intravascular Large B-Cell Lymphoma 53 0.039
404
MNN014 Mononeuritis 51 0.039
405
LPD004 Lipoid Nephrosis 51 0.039
406
P SZR006 Seizure Disorder 51 0.039
407
P CHR092 Chronic Myeloproliferative Disease 50 0.039
408
TRN007 Transsexualism 50 0.039
409
c SVR005 Severe Pre-Eclampsia 49 0.039
410
P PNC001 Pancytopenia 48 0.039
411
PRP016 Paraplegia 48 0.039
412
c HPT073 Hepatitis C Virus 48 0.039
413
RTN021 Retinal Vascular Occlusion 47 0.039
414
END021 Endomyocardial Fibrosis 47 0.039
415
SPL018 Splenomegaly 47 0.039
416
LMB062 Limb Ischemia 46 0.039
417
P HMG003 Hemoglobin E Disease 45 0.039
418
DYS157 Dysplasminogenemia 45 0.039
419
CRP018 Cor Pulmonale 45 0.039
420
OBS004 Obstructive Hydrocephalus 43 0.039
421
c ACT042 Acute Pyelonephritis 43 0.039
422
EPD005 Epidural Abscess 43 0.039
423
PLS018 Plasminogen Activator Inhibitor Type 1 Deficiency 43 0.039
424
CNT060 Central Serous Chorioretinopathy 42 0.039
425
HNC001 Henoch-Schoenlein Purpura 41 0.039
426
TYP015 Type 2b Von Willebrand Disease 40 0.039
427
INF013 Inferior Myocardial Infarction 40 0.039
428
TRC023 Trichinosis 40 0.039
429
BNM005 Bone Marrow Necrosis 39 0.039
430
CRB086 Cerebral Aneurysms 39 0.039
431
BCK006 Back Pain 39 0.039
432
PRS045 Prostatic Hypertrophy 38 0.039
433
HNS001 Hansen's Disease 37 0.039
434
STR044 Steroid-Resistant Nephrotic Syndrome 37 0.039
435
NRS005 Neurosarcoidosis 35 0.039
436
P LBY004 Labyrinthitis 34 0.039
437
LYM014 Lymphangitis 33 0.039
438
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 33 0.039
439
HMC020 Homocystinuria, B6-Responsive and Nonresponsive Types 33 0.039
440
P CRN035 Cranial Nerve Palsy 32 0.039
441
P INF069 Infantile Neuroaxonal Dystrophy 1 31 0.039
442
TYP018 Type 3 Von Willebrand Disease 30 0.039
443
c TWN006 Twin Twin Transfusion Syndrome 30 0.039
444
ALX001 Alexia 29 0.039
445
BSL004 Basilar Artery Occlusion 29 0.039
446
ETH009 Ethmoid Sinusitis 26 0.039
447
CHR158 Charles Bonnet Syndrome 26 0.039
448
P HYP589 Hypodysfibrinogenemia 25 0.039
449
PL2001 Pla2g6-Associated Neurodegeneration 25 0.039
450
THR089 Thrombophilia Due to Protein S Deficiency, Autosomal Dominant 25 0.039
451
ART007 Aorta Atresia 23 0.039
452
THR007 Thrombophlebitis Migrans 21 0.039
453
ABD009 Abducens Palsy 19 0.039
454
PRN017 Perianal Hematoma 14 0.039
455
CNG056 Congenital Antithrombin Deficiency 12 0.039
456
P ALZ001 Alzheimer's Disease 100 0.032
457
P TYP008 Type 1 Diabetes Mellitus 96 0.032
458
P PNC035 Pancreatic Cancer 93 0.032
459
P FML011 Familial Adenomatous Polyposis 89 0.032
460
P LFR001 Li-Fraumeni Syndrome 88 0.032
461
GLC006 Galactosemia 86 0.032
462
P TBR001 Tuberous Sclerosis 86 0.032
463
P MDL005 Medulloblastoma 80 0.032
464
P MNN012 Meningioma 78 0.032
465
P CLR023 Colorectal Cancer 77 0.032
466
P MST009 Mastocytosis 75 0.032
467
c PRM002 Primary Hyperoxaluria 74 0.032
468
NNH001 Non-Hodgkin Lymphoma 73 0.032
469
OBS002 Obsessive-Compulsive Disorder 73 0.032
470
CCC001 Coccidioidomycosis 72 0.032
471
P PRD006 Prader-Willi Syndrome 72 0.032
472
P DRM010 Dermatomyositis 71 0.032
473
GLL008 Gilles De La Tourette Syndrome 71 0.032
474
P HMN010 Hemangioma 71 0.032
475
P NRB001 Neuroblastoma 70 0.032
476
P MGR002 Migraine 70 0.032
477
P KDN017 Kidney Cancer 70 0.032
478
P END044 Endometriosis 70 0.032
479
CHL065 Cholangiocarcinoma 69 0.032
480
c HYP086 Hypothyroidism 69 0.032
481
NRL016 Neural Tube Defects 68 0.032
482
P PLY011 Polycystic Ovary Syndrome 68 0.032
483
SCR008 Scrub Typhus 68 0.032
484
CRY005 Cryptococcosis 68 0.032
485
ATM004 Autoimmune Thrombocytopenic Purpura 68 0.032
486
TKY001 Takayasu's Arteritis 68 0.032
487
P HYP056 Hypoglycemia 67 0.032
488
ERD001 Erdheim-Chester Disease 67 0.032
489
P PRD008 Periodontitis 67 0.032
490
P ANR007 Anorexia Nervosa 66 0.032
491
MLG056 Malignant Hyperthermia 66 0.032
492
OLL001 Ollier Disease 66 0.032
493
P GST044 Gastritis 66 0.032
494
STT001 Status Epilepticus 66 0.032
495
P HRD057 Hereditary Pancreatitis 66 0.032
496
ADN018 Adenoma 66 0.032
497
P INS005 Insulin Resistance 65 0.032
498
DBN001 Dubin-Johnson Syndrome 65 0.032
499
c HYP061 Hypertrophic Cardiomyopathy 65 0.032
500
CRB037 Cerebral Palsy 65 0.032
501
c EHL001 Ehlers-Danlos Syndrome 64 0.032
502
PMS001 Poems Syndrome 64 0.032
503
P ERY008 Erythromelalgia 64 0.032
504
P DYS007 Dyskeratosis Congenita 64 0.032
505
P OLG002 Oligodendroglioma 64 0.032
506
CRN018 Coronary Artery Anomaly 63 0.032
507
P CMP010 Complex Regional Pain Syndrome 63 0.032
508
CYS005 Cysticercosis 63 0.032
509
P RBL001 Rubella 63 0.032
510
CLN045 Colonic Benign Neoplasm 63 0.032
511
P ANP001 Anaplastic Large Cell Lymphoma 63 0.032
512
c MSC005 Muscular Dystrophy 62 0.032
513
HPT022 Hepatoblastoma 62 0.032
514
ART031 Aortic Coarctation 62 0.032
515
P MYP004 Myopathy 62 0.032
516
ADL030 Adult-Onset Still's Disease 62 0.032
517
P CRB042 Cerebellar Ataxia 62 0.032
518
MYL020 Myelomeningocele 62 0.032
519
c PLY014 Polycystic Kidney Disease 62 0.032
520
TXC005 Toxic Shock Syndrome 62 0.032
521
DWN001 Down Syndrome 62 0.032
522
P CRV035 Cervical Cancer 61 0.032
523
GNG013 Gingivitis 61 0.032
524
ASP003 Aseptic Meningitis 61 0.032
525
PLM001 Pulmonary Tuberculosis 61 0.032
526
c ANG015 Angioedema 61 0.032
527
P HYP080 Hypogonadism 60 0.032
528
c HPT003 Hepatitis a 59 0.032
529
c SYS004 Systemic Mastocytosis 59 0.032
530
CVR006 Cavernous Hemangioma 59 0.032
531
RHB003 Rhabdomyosarcoma 59 0.032
532
c ATX004 Ataxia 59 0.032
533
CNN005 Connective Tissue Disease 58 0.032
534
PRC012 Pericardial Effusion 58 0.032
535
P GLB002 Glioblastoma 58 0.032
536
P MYC008 Myocarditis 58 0.032
537
CCT002 Cicatricial Pemphigoid 58 0.032
538
P DBT005 Diabetes Insipidus 58 0.032
539
GLB015 Glioblastoma Multiforme 58 0.032
540
HYP266 Hypoxia 58 0.032
541
TNS005 Tonsillitis 57 0.032
542
PLS011 Plasmacytoma 57 0.032
543
c MLG002 Malignant Peritoneal Mesothelioma 57 0.032
544
ACT017 Acute Chest Syndrome 57 0.032
545
c HPT015 Hepatitis D 57 0.032
546
P PLC011 Pilocytic Astrocytoma 57 0.032
547
c CTR002 Cataract 57 0.032
548
MLG077 Malignant Peripheral Nerve Sheath Tumor 57 0.032
549
P SYR001 Syringomyelia 56 0.032
550
PYD001 Pyoderma Gangrenosum 56 0.032
551
TYP011 Typhus 56 0.032
552
MCR088 Microscopic Polyangiitis 56 0.032
553
BRN004 Brain Edema 55 0.032
554
P CHL066 Cholangitis 55 0.032
555
P HMN013 Hemangiopericytoma 55 0.032
556
LYM040 Lymphoblastic Lymphoma 54 0.032
557
END031 Endometrial Stromal Sarcoma 54 0.032
558
P ENC008 Encephalocele 54 0.032
559
CRV031 Cervical Adenocarcinoma 53 0.032
560
c NNT009 Neonatal Diabetes Mellitus 53 0.032
561
STS002 Situs Inversus 53 0.032
562
HMP005 Hemiplegia 53 0.032
563
TRN015 Transient Cerebral Ischemia 53 0.032
564
ATP002 Atopy 53 0.032
565
RFL001 Reflex Sympathetic Dystrophy 52 0.032
566
c HYD002 Hydronephrosis 52 0.032
567
HPT032 Hepatocellular Carcinoma, Somatic 52 0.032
568
ALC009 Alcoholic Liver Cirrhosis 52 0.032
569
CRN014 Cronkhite-Canada Syndrome 52 0.032
570
PYD002 Pyoderma 51 0.032
571
PLV003 Pelvic Inflammatory Disease 51 0.032
572
OBS001 Obstructive Jaundice 51 0.032
573
PLC007 Placental Abruption 51 0.032
574
CYS009 Cystadenoma 51 0.032
575
CLS010 Cluster Headache 50 0.032
576
GRM009 Germ Cell Tumors 50 0.032
577
c BCT007 Bacterial Meningitis 50 0.032
578
P APL006 Aplasia Cutis Congenita 50 0.032
579
SCT005 Scott Syndrome 50 0.032
580
P PRT096 Peritoneal Mesothelioma 50 0.032
581
SYN006 Synovial Sarcoma 50 0.032
582
SFT003 Soft Tissue Sarcoma 49 0.032
583
SMN007 Seminoma 49 0.032
584
c PSD003 Pseudohypoaldosteronism 49 0.032
585
MTS001 Mutism 49 0.032
586
PNV001 Panuveitis 48 0.032
587
BLD034 Bile Duct Carcinoma 48 0.032
588
PYM001 Pyomyositis 48 0.032
589
CNS002 Constrictive Pericarditis 48 0.032
590
P WRF002 Warfarin Sensitivity 47 0.032
591
P OVR046 Ovarian Cyst 47 0.032
592
URT010 Ureteral Obstruction 47 0.032
593
PNN001 Panniculitis 47 0.032
594
SPL004 Splenic Marginal Zone Lymphoma 47 0.032
595
P CRT018 Carotid Intimal Medial Thickness 47 0.032
596
HPT008 Hepatic Tuberculosis 47 0.032
597
P ATR005 Atrophic Gastritis 46 0.032
598
P HMR005 Hemorrhoid 46 0.032
599
LYM012 Lymphoplasmacytic Lymphoma 46 0.032
600
PNH001 Panhypopituitarism 46 0.032
601
HMN016 Hemangioendothelioma 46 0.032
602
PRT093 Proteus Syndrome, Somatic 45 0.032
603
PLR007 Pleural Empyema 45 0.032
604
ILS001 Ileus 45 0.032
605
SYS011 Systemic Lupus Erythematosus, Association with 44 0.032
606
LNG029 Lung Adenocarcinoma 44 0.032
607
TRN012 Transient Global Amnesia 44 0.032
608
CLL002 Collecting Duct Carcinoma 44 0.032
609
QDR001 Quadriplegia 44 0.032
610
NCR007 Necrotizing Fasciitis 44 0.032
611
P HRN001 Horner's Syndrome 43 0.032
612
ILC002 Ileocolitis 43 0.032
613
UTR039 Uterine Fibroid 42 0.032
614
WRF001 Warfarin Resistance 42 0.032
615
GPS001 Gapo Syndrome 42 0.032
616
HYP265 Hypotonia 41 0.032
617
BLR015 Blue Rubber Bleb Nevus Syndrome 41 0.032
618
FCL012 Facial Paralysis 40 0.032
619
LMY003 Leiomyomatosis 40 0.032
620
INT079 Intrahepatic Cholangiocarcinoma 40 0.032
621
CRB085 Cerebral Hemorrhage 39 0.032
622
FNT004 Fainting 39 0.032
623
VRL011 Viral Infectious Disease 39 0.032
624
PRS021 Prostatic Adenoma 38 0.032
625
ESN020 Eosinophilic Granulomatosis with Polyangiitis 38 0.032
626
GST053 Gastric Cancer 38 0.032
627
MYS004 Myiasis 37 0.032
628
ANG017 Angiolipoma 37 0.032
629
IPX001 Ipex Syndrome 37 0.032
630
VSC044 Visceral Myopathy 37 0.032
631
c SBC003 Subacute Bacterial Endocarditis 36 0.032
632
ADS002 Adie Syndrome 35 0.032
633
P MLD013 Mild Hemophilia a 35 0.032
634
MLK004 Malakoplakia 34 0.032
635
LYM005 Lymphocele 34 0.032
636
HPT012 Hepatocellular Fibrolamellar Carcinoma 33 0.032
637
P PRX010 Paroxysmal Ventricular Fibrillation 33 0.032
638
HPT066 Hepatoportal Sclerosis 32 0.032
639
HYP319 Hypereosinophilic Syndrome, Idiopathic, Resistant to Imatinib 32 0.032
640
P ATM020 Autoimmune Enteropathy 31 0.032
641
TYP017 Type 2n Von Willebrand Disease 31 0.032
642
TYP014 Type 2a Von Willebrand Disease 30 0.032
643
TYP016 Type 2m Von Willebrand Disease 30 0.032
644
NRR001 Neuroretinitis 29 0.032
645
WND002 Wandering Spleen 28 0.032
646
TFT003 Tufting Enteropathy 28 0.032
647
PRR008 Periarteritis Nodosa 28 0.032
648
FBR028 Fibrosing Mediastinitis 28 0.032
649
HNM002 Hinman Syndrome 28 0.032
650
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.032
651
PRM008 Parametritis 27 0.032
652
c ACT036 Acute Cholangitis 26 0.032
653
STR077 Streptococcal Toxic-Shock Syndrome 24 0.032
654
THR067 Thrombophilia Due to Protein C Deficiency, Autosomal Dominant 24 0.032
655
PRF003 Piriformis Syndrome 22 0.032
656
c MLT009 Multiple Cranial Nerve Palsy 22 0.032
657
c ACT035 Acute Frontal Sinusitis 22 0.032
658
SCT001 Sciatic Neuropathy 21 0.032
659
MSN003 Mesenteric Vascular Occlusion 21 0.032
660
HMC016 Homocystinuria Due to Cbs Deficiency 20 0.032
661
HMC012 Hemicrania Continua 20 0.032
662
MXD035 Mixed-Type Autoimmune Hemolytic Anemia 20 0.032
663
MNN005 Meningovascular Neurosyphilis 19 0.032
664
MCR033 Macrocephaly-Capillary Malformation 15 0.032
665
PLM062 Pulmonary Hyalinizing Granuloma 15 0.032
666
CGH002 Cough Headache 15 0.032
667
OCL024 Ocular Neuromyotonia 14 0.032
668
SNG003 Single Ventricular Heart 14 0.032
669
CRT056 Carotidynia 13 0.032
670
NNT044 Neonatal Antiphospholipid Syndrome 12 0.032
671
MTH028 Mthfr Thermolabile Variant 10 0.032
672
THR088 Thrombophilia Due to Protein S Deficiency, Autosomal Recessive 8 0.032
673
ACT174 Acute Peripheral Arterial Occlusion 8 0.032
674
c TYP009 Type 2 Diabetes Mellitus 100 0.022
675
P PRK002 Parkinson's Disease 93 0.022
676
P DLT002 Dilated Cardiomyopathy 88 0.022
677
FBR012 Fabry Disease 86 0.022
678
P HMC003 Hemochromatosis 83 0.022
679
P RTT002 Rett Syndrome 83 0.022
680
c NNN003 Noonan Syndrome 80 0.022
681
P WSK001 Wiskott-Aldrich Syndrome 79 0.022
682
CNG034 Congestive Heart Failure 78 0.022
683
ACT033 Acute Intermittent Porphyria 78 0.022
684
LSC001 Lesch-Nyhan Syndrome 78 0.022
685
PTZ001 Peutz-Jeghers Syndrome 78 0.022
686
P FRG001 Fragile X Syndrome 76 0.022
687
CRB011 Cerebrotendinous Xanthomatosis 76 0.022
688
P RBN001 Rubinstein-Taybi Syndrome 76 0.022
689
THY028 Thyroid Cancer 75 0.022
690
P CSH001 Cushing's Syndrome 75 0.022
691
P MLR004 Malaria 75 0.022
692
DCH001 Duchenne Muscular Dystrophy 75 0.022
693
P SRC013 Sarcoidosis 75 0.022
694
P ALP006 Alpha Thalassemia 75 0.022
695
P LYM007 Lymphangioleiomyomatosis 74 0.022
696
SVR004 Severe Combined Immunodeficiency 74 0.022
697
c OST005 Osteogenesis Imperfecta 74 0.022
698
P PRM006 Primary Biliary Cirrhosis 73 0.022
699
P MYS005 Myositis 70 0.022
700
BLL006 Bullous Pemphigoid 70 0.022
701
P RTH001 Rothmund-Thomson Syndrome 70 0.022
702
P STM004 Stomach Cancer 69 0.022
703
LKC001 Leukocyte Adhesion Deficiency 69 0.022
704
PLY017 Polyarteritis Nodosa 69 0.022
705
DNY001 Denys-Drash Syndrome 69 0.022
706
LMY002 Leiomyoma 69 0.022
707
P AMY004 Amyloidosis 68 0.022
708
P INF038 Influenza 68 0.022
709
MLB002 Male Breast Cancer 68 0.022
710
ACT010 Acth-Secreting Pituitary Adenoma 68 0.022
711
SPN038 Spina Bifida 68 0.022
712
P ATP001 Atopic Dermatitis 67 0.022
713
ACT049 Acute Disseminated Encephalomyelitis 67 0.022
714
P HYP117 Hypertriglyceridemia 67 0.022
715
MGL001 Megaloblastic Anemia 66 0.022
716
c SPN046 Spinal Muscular Atrophy 66 0.022
717
P CHR089 Chronic Kidney Failure 66 0.022
718
c UVT001 Uveitis 66 0.022
719
BRN028 Brain Cancer 65 0.022
720
c SCL016 Scleroderma 65 0.022
721
P ALP009 Alopecia Areata 65 0.022
722
ARG002 Argininosuccinic Aciduria 65 0.022
723
P CNG042 Congenital Central Hypoventilation Syndrome 65 0.022
724
ARS001 Aarskog-Scott Syndrome 64 0.022
725
CHL014 Cholera 64 0.022
726
MXD005 Mixed Connective Tissue Disease 64 0.022
727
BBS001 Babesiosis 64 0.022
728
P ADL010 Adult Respiratory Distress Syndrome 64 0.022
729
P ART023 Arthropathy 64 0.022
730
HV1006 Hiv-1 64 0.022
731
BLL003 Bell's Palsy 64 0.022
732
SQM007 Squamous Cell Carcinoma of the Head and Neck 63 0.022
733
CMP002 Campylobacteriosis 63 0.022
734
PSR002 Psoriasis 63 0.022
735
P CHN012 Chondrosarcoma 63 0.022
736
c PRP029 Porphyria 63 0.022
737
GRY002 Gray Platelet Syndrome 63 0.022
738
KRN002 Kearns-Sayre Syndrome 63 0.022
739
STS003 Sitosterolemia 62 0.022
740
P GTR002 Goiter 62 0.022
741
c DMN001 Diamond-Blackfan Anemia 62 0.022
742
MLD001 Melioidosis 62 0.022
743
GLC003 Glucose Intolerance 62 0.022
744
BCK001 Becker Muscular Dystrophy 61 0.022
745
SRS001 Serous Cystadenocarcinoma 61 0.022
746
LGN001 Legionnaires' Disease 61 0.022
747
BRC012 Brucellosis 61 0.022
748
c DST002 Distal Arthrogryposis 61 0.022
749
P BRN009 Burning Mouth Syndrome 60 0.022
750
MLL005 Miller-Dieker Syndrome 60 0.022
751
NRN004 Neuroendocrine Tumor 60 0.022
752
c OST026 Osteogenesis Imperfecta Type I 60 0.022
753
CRB021 Cerebral Malaria 60 0.022
754
DNG003 Dengue Disease 60 0.022
755
JCB001 Jacobsen Syndrome 60 0.022
756
ACR008 Acrocallosal Syndrome 60 0.022
757
MCS003 Mucous Membrane Pemphigoid 60 0.022
758
MGC001 Megacolon 60 0.022
759
CRT002 Cartilage-Hair Hypoplasia 60 0.022
760
c TRT010 Teratoma 59 0.022
761
DST005 Diastrophic Dysplasia 59 0.022
762
ECH003 Echinococcosis 59 0.022
763
AMN001 Amenorrhea 59 0.022
764
P PRM124 Primary Hyperoxaluria Type 1 59 0.022
765
CHL068 Cholestasis 59 0.022
766
BLM002 Bulimia Nervosa 59 0.022
767
c CNG015 Congenital Diaphragmatic Hernia 59 0.022
768
NRN001 Neuroendocrine Carcinoma 59 0.022
769
RTN025 Retinoschisis 59 0.022
770
MYX005 Myxoid Liposarcoma 59 0.022
771
ANN002 Anencephaly 59 0.022
772
EXT010 Extramedullary Plasmacytoma 59 0.022
773
NTH001 Netherton Syndrome 58 0.022
774
OBS061 Obstructive Sleep Apnea 58 0.022
775
P SYP003 Syphilis 58 0.022
776
P HRD012 Hereditary Elliptocytosis 58 0.022
777
ISC006 Ischemic Heart Disease 58 0.022
778
HYP003 Hypermethioninemia 58 0.022
779
NRL005 Neurilemmoma 58 0.022
780
c HRD002 Hereditary Angioedema 58 0.022
781
EPT020 Epithelioid Hemangioendothelioma 58 0.022
782
HRP004 Herpes Zoster 58 0.022
783
P SDR002 Siderosis 58 0.022
784
P DND001 Dandy-Walker Syndrome 58 0.022
785
MCN007 Meconium Aspiration Syndrome 57 0.022
786
P ACT009 Acute Monocytic Leukemia 57 0.022
787
c THR003 Thoracic Aortic Aneurysm 57 0.022
788
NTR003 Natural Killer Cell Leukemia 57 0.022
789
ANK001 Ankylosis 57 0.022
790
c MNC007 Monocytic Leukemia 57 0.022
791
c PST005 Posterior Uveitis 57 0.022
792
RNL007 Renal Tubular Acidosis 57 0.022
793
P PLY006 Polydactyly 57 0.022
794
DBT008 Diabetic Angiopathy 57 0.022
795
CNG048 Congenital Hepatic Fibrosis 57 0.022
796
DNG001 Dengue Shock Syndrome 57 0.022
797
GST037 Gastroparesis 56 0.022
798
c FML035 Familial Hyperlipidemia 56 0.022
799
CLC001 Calciphylaxis 56 0.022
800
ART017 Aortic Disease 56 0.022
801
BRK001 Brooke-Spiegler Syndrome 56 0.022
802
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 56 0.022
803
ILT001 Ileitis 56 0.022
804
GST050 Gastrointestinal System Disease 56 0.022
805
JPN002 Japanese Encephalitis 55 0.022
806
ACT095 Acute Biphenotypic Leukemia 55 0.022
807
MCR004 Macroglobulinemia 55 0.022
808
c HRM001 Hermansky-Pudlak Syndrome 55 0.022
809
MTN003 Motion Sickness 55 0.022
810
IMP005 Impotence 55 0.022
811
FBR003 Fibrous Histiocytoma 55 0.022
812
CYS014 Cystadenocarcinoma 55 0.022
813
MCN001 Mucinous Adenocarcinoma 55 0.022
814
LGN002 Legionellosis 55 0.022
815
c ADL052 Adult Acute Lymphocytic Leukemia 54 0.022
816
SPR004 Supravalvular Aortic Stenosis 54 0.022
817
P VNT002 Ventricular Septal Defect 54 0.022
818
STT004 Steatorrhea 54 0.022
819
ORL011 Oral Cancer 54 0.022
820
P INT072 Intestinal Pseudo-Obstruction 54 0.022
821
P MSC003 Muscular Atrophy 54 0.022
822
PPT005 Peptic Ulcer Disease 54 0.022
823
END020 Endocardial Fibroelastosis 54 0.022
824
P DYS142 Dyskeratosis Congenita, Autosomal Recessive 4 53 0.022
825
HNT002 Hantavirus Pulmonary Syndrome 53 0.022
826
KLT001 Klatskin's Tumor 53 0.022
827
MCR010 Microcephaly 53 0.022
828
c CNT048 Central Hypoventilation Syndrome 53 0.022
829
STN007 Stenotrophomonas Maltophilia 53 0.022
830
c RST002 Restrictive Cardiomyopathy 53 0.022
831
PRT029 Parathyroid Adenoma 53 0.022
832
CLN015 Colon Adenocarcinoma 52 0.022
833
GRW007 Growth Hormone Deficiency 52 0.022
834
ACS001 Acoustic Neuroma 52 0.022
835
FML164 Familial Hdl Deficiency 52 0.022
836
MYC005 Myocardial Stunning 52 0.022
837
P STR020 Strabismus 52 0.022
838
MCL003 Macular Holes 52 0.022
839
SHR001 Short Bowel Syndrome 52 0.022
840
NPH010 Nephrosclerosis 52 0.022
841
c DRR001 Diarrhea 52 0.022
842
PRG008 Paragonimiasis 52 0.022
843
c CMP058 Complex Regional Pain Syndrome Type 1 51 0.022
844
KMR001 Kimura Disease 51 0.022
845
c TLN008 Telangiectasia, Hereditary Hemorrhagic, Type 5 51 0.022
846
DGS001 Degos Disease 51 0.022
847
WBR001 Weber Syndrome 51 0.022
848
P CST002 Castleman's Disease 51 0.022
849
LPR001 Lepromatous Leprosy 51 0.022
850
c CRB126 Cerebral Cavernous Malformation 51 0.022
851
RTN001 Retinal Vasculitis 51 0.022
852
c EPS003 Episodic Ataxia 51 0.022
853
c HYP011 Hyperlipoproteinemia Type Iii 50 0.022
854
PRT026 Parotitis 50 0.022
855
INF058 Inflammatory Myofibroblastic Tumor 50 0.022
856
LFT009 Left Ventricular Outflow Tract Obstruction 50 0.022
857
ERY017 Erythema Elevatum Diutinum 50 0.022
858
TLN003 Telangiectasis 49 0.022
859
TRN044 Transposition of the Great Arteries 49 0.022
860
c INT060 Intestinal Atresia 49 0.022
861
DVR002 Diverticulitis 49 0.022
862
c CNT035 Central Nervous System Disease 49 0.022
863
CNV002 Conversion Disorder 49 0.022
864
CRT049 Critical Limb Ischemia 49 0.022
865
PNC033 Pancreas Adenocarcinoma 49 0.022
866
c ACT150 Acute Adrenal Insufficiency 49 0.022
867
SML026 Small Fiber Neuropathy 49 0.022
868
GNT031 Genitopatellar Syndrome 49 0.022
869
PLM010 Pulmonary Edema 49 0.022
870
IMP002 Imperforate Anus 48 0.022
871
NNT016 Neonatal Hemochromatosis 48 0.022
872
CRN027 Corneal Neovascularization 48 0.022
873
BRN014 Bronchopneumonia 48 0.022
874
P HRD066 Hereditary Angioedema Type Iii 48 0.022
875
PRN021 Paranasal Sinus Disease 48 0.022
876
CRT008 Carotid Artery Dissection 48 0.022
877
MNC006 Monoclonal Gammopathy of Uncertain Significance 47 0.022
878
c MLG086 Malignant Hyperthermia Susceptibility 47 0.022
879
P TRN034 Transverse Myelitis 47 0.022
880
MYS001 Myositis Ossificans 47 0.022
881
HYP054 Hypochromic Anemia 47 0.022
882
TBR008 Tuberculous Peritonitis 47 0.022
883
MNN009 Meningoencephalitis 47 0.022
884
SCR024 Sacrococcygeal Teratoma 47 0.022
885
DFN221 Deafness Dystonia Syndrome 47 0.022
886
P HMR003 Hemorrhagic Disease 46 0.022
887
MNN017 Mononeuropathy 46 0.022
888
QBC001 Quebec Platelet Disorder 46 0.022
889
GLM037 Glioma Somatic 46 0.022
890
BWN003 Bowenoid Papulosis 46 0.022
891
PLM052 Pulmonary Arteriovenous Malformation 46 0.022
892
WLL004 Wallerian Degeneration 46 0.022
893
ART004 Aortic Atherosclerosis 46 0.022
894
P NRL007 Neurologic Diseases 45 0.022
895
INF034 Infective Endocarditis 45 0.022
896
P MYH004 Myh9 Related Thrombocytopenia 45 0.022
897
HRS011 Horseshoe Kidney 45 0.022
898
NNT020 Neonatal Intrahepatic Cholestasis Caused by Citrin Deficiency 45 0.022
899
c JVN024 Juvenile Hereditary Hemochromatosis 45 0.022
900
LYM011 Lymphogranuloma Venereum 45 0.022
901
UTR024 Uterine Carcinosarcoma 45 0.022
902
c PNC102 Pancreatitis, Chronic 45 0.022
903
CRB088 Cerebral Atrophy 44 0.022
904
FTT001 Fatty Liver Disease 44 0.022
905
SYN036 Syncope 44 0.022
906
PLC005 Placental Insufficiency 44 0.022
907
CHN015 Chondrodysplasia 44 0.022
908
c APH002 Aphasia 44 0.022
909
RTC005 Reticulosarcoma 44 0.022
910
CHR010 Chorioangioma 44 0.022
911
c CHR342 Chiari Malformation 44 0.022
912
CRB004 Cerebral Artery Occlusion 44 0.022
913
ADN027 Adenomyosis 43 0.022
914
CRN030 Coronary Stenosis 43 0.022
915
PLR005 Pleuropneumonia 43 0.022
916
DFC001 Defective Apolipoprotein B-100 43 0.022
917
LMB052 Lumbar Disc Herniation 43 0.022
918
INT071 Intestinal Perforation 42 0.022
919
ESP002 Esophageal Varix 42 0.022
920
P VGN017 Vaginal Cancer 42 0.022
921
CRD016 Cardiac Rupture 41 0.022
922
XNT001 Xanthogranulomatous Pyelonephritis 41 0.022
923
P BRN035 Brain Stem Glioma 41 0.022
924
HMT018 Hematopoietic Stem Cell Transplantation 41 0.022
925
GST040 Gastric Adenocarcinoma 41 0.022
926
P MNN007 Meningocele 41 0.022
927
WTH001 Withdrawal Disorder 41 0.022
928
RBF001 Riboflavin Deficiency 41 0.022
929
ACL001 Acalculous Cholecystitis 41 0.022
930
MCK002 Meckel's Diverticulum 41 0.022
931
STR037 Stress Cardiomyopathy 41 0.022
932
HMP018 Hemophilic Arthropathy 41 0.022
933
INP001 Inappropriate Adh Syndrome 41 0.022
934
GLY015 Glycine N-Methyltransferase Deficiency 40 0.022
935
GST071 Gastrointestinal Carcinoma 40 0.022
936
SCT002 Scotoma 40 0.022
937
LNS001 Lens Subluxation 40 0.022
938
P DPH016 Diaphragmatic Hernia 3 40 0.022
939
KDN015 Kidney Angiomyolipoma 40 0.022
940
VTM001 Vitamin K Deficiency Hemorrhagic Disease 40 0.022
941
ART012 Aortitis 39 0.022
942
TBR006 Tuberculoid Leprosy 39 0.022
943
P THR045 Thrombotic Thrombocytopenic Purpura, Congenital 39 0.022
944
ALC005 Alcoholic Pancreatitis 39 0.022
945
P CHR038 Chronic Maxillary Sinusitis 39 0.022
946
c TYP002 Type Vi Ehlers-Danlos Syndrome 39 0.022
947
PRT086 Partial Hydatidiform Mole 39 0.022
948
SGN002 Signet Ring Cell Adenocarcinoma 39 0.022
949
CHL061 Childhood Leukemia 39 0.022
950
CMB021 Combined Pituitary Hormone Deficiency 38 0.022
951
SPR066 Superficial Siderosis 38 0.022
952
ADN002 Adenoiditis 38 0.022
953
DXT002 Dextrocardia with Situs Inversus 38 0.022
954
BRN055 Bronchogenic Cyst 38 0.022
955
ERY045 Erythrocytosis, Somatic 38 0.022
956
P SYS007 Systemic Capillary Leak Syndrome 37 0.022
957
P HYP071 Hypersensitivity Reaction Type Ii Disease 37 0.022
958
CTR003 Citrin Deficiency 37 0.022
959
FTD001 Foot Drop 37 0.022
960
c FML162 Familial Mediterranean Fever, Ad 37 0.022
961
PRL008 Paralytic Ileus 36 0.022
962
HYP143 Hypomyelination and Congenital Cataract 36 0.022
963
CNG069 Congenital Cytomegalovirus 36 0.022
964
OPT006 Optic Nerve Disease 36 0.022
965
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 36 0.022
966
PTT021 Pituitary Hormone Deficiency, Combined 2 36 0.022
967
RHS001 Rh Isoimmunization 35 0.022
968
FTL012 Fetal and Neonatal Alloimmune Thrombocytopenia 34 0.022
969
INT042 Internuclear Ophthalmoplegia 34 0.022
970
CGN006 Cogan Syndrome 34 0.022
971
SPR007 Superior Mesenteric Artery Syndrome 34 0.022
972
PLY024 Polymicrogyria 34 0.022
973
HMG020 Hmg Coa Lyase Deficiency 33 0.022
974
CNG219 Congenital Aural Atresia 33 0.022
975
NTR005 Nutritional Deficiency Disease 33 0.022
976
ANG049 Angioedema Induced by Ace Inhibitors 33 0.022
977
c SVR057 Severe Hemophilia B 33 0.022
978
NRC019 Neurocutaneous Melanosis, Somatic 32 0.022
979
ULN001 Ulnar Neuropathy 32 0.022
980
TST021 Testicular Germ Cell Tumor 31 0.022
981
P CHR454 Chiari Malformation Type 1 31 0.022
982
CRN185 Craniofacial Deafness Hand Syndrome 31 0.022
983
SPL007 Splenic Abscess 31 0.022
984
ADT003 Auditory System Disease 30 0.022
985
MGL023 Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome, Somatic 30 0.022
986
P 49X002 49,xxxxy Syndrome 30 0.022
987
PNG002 Pain Agnosia 30 0.022
988
CNG134 Congenitally Corrected Transposition of the Great Arteries 30 0.022
989
P CMM008 Communicating Hydrocephalus 30 0.022
990
PRN037 Prinzmetal's Variant Angina 30 0.022
991
TXC001 Toxic Megacolon 30 0.022
992
SBC014 Subclavian Steal Syndrome 29 0.022
993
DYS003 Dysgraphia 29 0.022
994
P DCR004 Dacryocystitis 28 0.022
995
HMX002 Heme Oxygenase-1 Deficiency 28 0.022
996
BLD052 Blood Group Incompatibility 28 0.022
997
MLN013 Melanoma Metastasis 28 0.022
998
SPR032 Superficial Siderosis of the Central Nervous System 28 0.022
999
GNT005 Giant Hemangioma 28 0.022
1000
CRT045 Creatine Phosphokinase, Elevated Serum 28 0.022
1001
CRN019 Coronary Artery Vasospasm 27 0.022
1002
CRT028 Cor Triatriatum 27 0.022
1003
ANT013 Anterior Spinal Artery Syndrome 26 0.022
1004
RHB020 Rhabdomyosarcoma, Somatic 26 0.022
1005
CPL011 Capillary Malformations, Congenital, 1, Somatic, Mosaic 26 0.022
1006
P CHR097 Chronic Purulent Otitis Media 26 0.022
1007
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 26 0.022
1008
MCR216 Microcephaly with or Without Chorioretinopathy, Lymphedema, or Mental Retardation 26 0.022
1009
c MLD014 Mild Hemophilia B 25 0.022
1010
ABD002 Abducens Nerve Disease 25 0.022
1011
CHR034 Chromophobe Adenoma 25 0.022
1012
HMR039 Hemorrhage, Intracerebral 25 0.022
1013
PRN007 Perinephritis 24 0.022
1014
EMB002 Embryoma 24 0.022
1015
P FML179 Familial Erythrocytosis 2 24 0.022
1016
STR080 Stroke, Hemorrhagic 23 0.022
1017
ANG022 Angel Shaped Phalangoepiphyseal Dysplasia 23 0.022
1018
MSN002 Mesenteric Lymphadenitis 23 0.022
1019
SBS002 Substernal Goiter 23 0.022
1020
c PST001 Posterior Myocardial Infarction 23 0.022
1021
MYX006 Myxoid Leiomyosarcoma 22 0.022
1022
VRT001 Vertebral Artery Occlusion 22 0.022
1023
MLT037 Multifocal Lymphangioendotheliomatosis with Thrombocytopenia 22 0.022
1024
PLY004 Polyp of Corpus Uteri 21 0.022
1025
ACT201 Acute Posterior Multifocal Placoid Pigment Epitheliopathy 21 0.022
1026
CNG171 Congenital Plasminogen Deficiency 21 0.022
1027
RHM007 Rheumatic Congestive Heart Failure 21 0.022
1028
PRP021 Peripheral Nervous System Neoplasm 21 0.022
1029
SBC002 Subclavian Artery Aneurysm 20 0.022
1030
P HMN004 Hemangioma of Liver 20 0.022
1031
P OCL041 Oculomotor Apraxia Cogan Type 20 0.022
1032
QLT001 Qualitative Platelet Defect 20 0.022
1033
RCT009 Rectosigmoid Cancer 20 0.022
1034
MDN008 Median Arcuate Ligament Syndrome 19 0.022
1035
PLS001 Pulsating Exophthalmos 19 0.022
1036
HYP015 Hyperlucent Lung 19 0.022
1037
INT147 Intrauterine Growth Restriction, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 19 0.022
1038
MNG003 Mungan Syndrome 19 0.022
1039
BNT001 Banti's Syndrome 19 0.022
1040
FRN014 Fournier Gangrene 18 0.022
1041
ART109 Arterial Thoracic Outlet Syndrome 18 0.022
1042
FXL001 Foix-Alajouanine Syndrome 18 0.022
1043
PNT023 Pontine Hemorrhage 18 0.022
1044
CHR076 Choriocarcinoma of the Testis 18 0.022
1045
INT010 Intracranial Embolism 18 0.022
1046
CNT067 Central Cord Syndrome 18 0.022
1047
CRD023 Cardiomyopathy Cataract Hip Spine Disease 17 0.022
1048
CNG298 Congenital Pancreatic Cyst 17 0.022
1049
RNL001 Renal Artery Obstruction 17 0.022
1050
OTP003 Oto-Palatal-Digital Syndrome 17 0.022
1051
MGL021 Megalencephaly-Capillary Malformation Syndrome 16 0.022
1052
48X002 48,xxxy Syndrome 16 0.022
1053
CNG092 Congenital Extrahepatic Portosystemic Shunt 16 0.022
1054
TMP006 Temporomandibular Ankylosis 16 0.022
1055
XLN139 X-Linked Intellectual Disability - Macrocephaly - Macroorchidism 15 0.022
1056
DRL001 Dural Sinus Malformation 15 0.022
1057
GST016 Gastric Signet Ring Cell Adenocarcinoma 14 0.022
1058
BLT017 Bilateral Massive Adrenal Hemorrhage 14 0.022
1059
CVR001 Cavernous Sinus Meningioma 14 0.022
1060
CYS035 Cystic Adventitial Disease 12 0.022
1061
c THR081 Thrombophilia Due to Factor V Leiden 12 0.022
1062
c EHL052 Ehlers–danlos Syndrome, Vascular Type 12 0.022
1063
INF001 Infarct of Liver 12 0.022
1064
INT055 Intravascular Fasciitis 10 0.022
1065
c PRT053 Portal Hypertension Due to Infrahepatic Block 4 0.022