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

1061 hits were found for 'thrombosis'

# Family MCID Name MIFTS Score
1
SGT001 Sagittal Sinus Thrombosis 45 5.779
2
PRT018 Portal Vein Thrombosis 57 5.529
3
INT078 Intracranial Thrombosis 30 5.216
4
CRN017 Coronary Thrombosis 57 5.176
5
LTR002 Lateral Sinus Thrombosis 23 4.606
6
CVR002 Cavernous Sinus Thrombosis 29 4.307
7
CRT004 Carotid Artery Thrombosis 45 4.167
8
HPT002 Hepatic Vein Thrombosis 65 4.129
9
VNS009 Venous Thrombosis 43 3.904
10
INT076 Intracranial Sinus Thrombosis 14 3.427
11
CRB132 Cerebral Sinovenous Thrombosis 32 3.224
12
VNS011 Venous Thrombosis, Protection Against 6 2.735
13
THR062 Thrombosis, Hyperhomocysteinemic 23 2.687
14
DPV002 Deep Venous Thrombosis, Protection Against 6 2.633
15
DYS078 Dysfibrinogenemia, Alpha Type, Causing Recurrent Thrombosis 5 2.633
16
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 5 2.633
17
VNS012 Venous Thoracic Outlet Syndrome 17 1.862
18
MND006 Mondor Disease 14 1.862
19
CRB009 Cerebritis 56 0.506
20
PRT014 Protein S Deficiency 66 0.283
21
c HPT021 Hepatitis 75 0.264
22
PRT011 Protein C Deficiency 60 0.264
23
P THR015 Thrombophilia 66 0.258
24
P MYC007 Myocardial Infarction 88 0.255
25
IDP042 Idiopathic Recurrent Stupor 15 0.248
26
TYP018 Type 3 Von Willebrand Disease 23 0.246
27
PLM033 Pulmonary Embolism 68 0.245
28
ANT006 Antiphospholipid Syndrome 67 0.244
29
c THR014 Thrombocytopenia 67 0.237
30
VNS010 Venous Thromboembolism 42 0.237
31
INF133 Inferior Vena Cava Interruption 27 0.221
32
END072 Endotheliitis 47 0.220
33
HPT023 Hepatocellular Carcinoma 89 0.197
34
HMC004 Homocysteine Plasma Level 27 0.195
35
P HYP075 Hypertension 86 0.190
36
ANT009 Antithrombin Iii Deficiency 57 0.190
37
PRX023 Paroxysmal Nocturnal Hemoglobinuria, Somatic 28 0.182
38
SPS077 Sepsis 58 0.179
39
HYP037 Hyperhomocysteinemia 55 0.177
40
PRP034 Purpura Fulminans 38 0.175
41
VND001 Vein Disease 48 0.174
42
c LPS004 Lupus Erythematosus 73 0.172
43
P SYS001 Systemic Lupus Erythematosus 87 0.170
44
c ACT075 Acute Myocardial Infarction 61 0.165
45
c NPH012 Nephrotic Syndrome 66 0.161
46
ULC004 Ulcerative Colitis 72 0.146
47
THR079 Thromboembolism 50 0.146
48
PSD002 Pseudotumor Cerebri 47 0.146
49
c HPT003 Hepatitis a 60 0.145
50
P LKM002 Leukemia 79 0.143
51
INT075 Intracranial Hypertension 59 0.143
52
c AFB001 Afibrinogenemia 48 0.143
53
PRG060 Pregnancy Loss 38 0.143
54
THR004 Thrombocytosis 63 0.141
55
ANK002 Ankylosing Spondylitis 75 0.140
56
THR035 Thrombasthenia 37 0.140
57
c PNC044 Pancreatitis 67 0.138
58
PRP030 Purpura 67 0.138
59
c PLY018 Polycythemia 61 0.138
60
FCT013 Factor V Leiden Thrombophilia 35 0.138
61
PLY001 Polycythemia Vera 83 0.136
62
THR016 Thrombophlebitis 65 0.136
63
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 44 0.136
64
CNT060 Central Serous Chorioretinopathy 28 0.132
65
HMG002 Hemoglobinuria 55 0.131
66
LVR012 Liver Cirrhosis 75 0.129
67
THR013 Thoracic Outlet Syndrome 54 0.127
68
P PRT013 Portal Hypertension 67 0.125
69
MTH044 Mthfr Gene Mutation 25 0.125
70
VSC007 Vascular Disease 72 0.123
71
ATH003 Atherosclerosis 71 0.123
72
P HMP004 Hemophilia B 80 0.121
73
c ACT073 Acute Leukemia 62 0.121
74
MYC065 Myocardial Infarction, Decreased 30 0.121
75
PRC016 Pre-Eclampsia 75 0.119
76
BRN026 Branch Retinal Artery Occlusion 41 0.119
77
CTS005 Catastrophic Antiphospholipid Syndrome 35 0.119
78
SYS011 Systemic Lupus Erythematosus, Association with 14 0.119
79
STR067 Stroke, Ischemic 74 0.117
80
DSS009 Disseminated Intravascular Coagulation 66 0.117
81
CHR466 Chronic Thromboembolic Pulmonary Hypertension 43 0.117
82
PRP028 Peripheral Vertigo 36 0.117
83
c MNN013 Meningitis 71 0.113
84
FCT006 Factor V Deficiency 64 0.113
85
ISC004 Ischemia 64 0.113
86
RTN023 Retinitis 61 0.113
87
IRN001 Iron Deficiency Anemia 61 0.113
88
CLL003 Cellulitis 56 0.113
89
EVN001 Evans' Syndrome 54 0.110
90
HPR003 Heparin-Induced Thrombocytopenia 45 0.110
91
NNT024 Neonatal Stroke 40 0.110
92
INT003 Intracranial Hypotension 28 0.110
93
SDD005 Sudden Cardiac Death Multi-Gene Panels 21 0.110
94
P ATX002 Ataxia Telangiectasia 93 0.108
95
BLD054 Blood Protein Disease 41 0.108
96
HMR001 Hemorrhagic Thrombocythemia 34 0.108
97
c PRN026 Porencephaly 32 0.108
98
ADS010 Aids, Slow Progression to 26 0.108
99
c ACQ012 Acquired Angioedema 23 0.108
100
CRN211 Coronary Artery Disease 72 0.106
101
OVR029 Ovarian Hyperstimulation Syndrome 70 0.104
102
P INF037 Inflammatory Bowel Disease 50 0.104
103
RLP001 Relapsing Polychondritis 69 0.101
104
OTT002 Otitis Media 60 0.101
105
c ART084 Arteriovenous Fistula 47 0.101
106
CRN006 Coronary Aneurysm 47 0.101
107
CRT015 Carotid Artery Occlusion 43 0.101
108
ERL004 Early Yaws 33 0.101
109
GNR028 Generalized Essential Telangiectasia 16 0.101
110
FCT004 Factor Xii Deficiency 66 0.099
111
P HMC002 Homocystinuria 61 0.099
112
PTN001 Patent Foramen Ovale 60 0.099
113
P ISC002 Ischemic Optic Neuropathy 57 0.099
114
SPT013 Septic Shock 48 0.099
115
NDL013 Nodular Regenerative Hyperplasia 42 0.099
116
P SCH018 Schizencephaly 38 0.099
117
c SVR056 Severe Hemophilia a 37 0.099
118
MYC020 Mycobacterium Tuberculosis, Susceptibility to Infection by 36 0.099
119
HMC014 Homocysteinemia 35 0.099
120
CRK001 Cork-Handlers' Disease 32 0.099
121
ACN002 Acanthosis Nigricans 73 0.094
122
c RTN014 Retinal Artery Occlusion 53 0.094
123
CHL079 Children's Interstitial Lung Disease 46 0.094
124
P THR045 Thrombotic Thrombocytopenic Purpura, Congenital 43 0.094
125
SPP008 Suppurative Otitis Media 40 0.094
126
c ACQ014 Acquired Hemophilia 35 0.094
127
P INF069 Infantile Neuroaxonal Dystrophy 1 32 0.094
128
INF034 Infective Endocarditis 50 0.091
129
PRN037 Prinzmetal's Variant Angina 19 0.091
130
CRH001 Crohn's Disease 83 0.088
131
THR006 Thromboangiitis Obliterans 75 0.088
132
c LCL006 Localized Scleroderma 68 0.088
133
c ACT027 Acute Pancreatitis 63 0.088
134
SCN006 Secondary Syphilis 55 0.088
135
MLK003 Melkersson-Rosenthal Syndrome 48 0.088
136
BRS090 Breast Reconstruction 42 0.088
137
LMR001 Lemierre's Syndrome 35 0.088
138
PHL005 Phlebitis 34 0.088
139
ORB006 Orbital Cellulitis 29 0.088
140
CRN224 Craniofaciofrontodigital Syndrome 23 0.088
141
INT206 Intellectual Deficit, X-Linked - Macrocephaly - Macro-Orchidism 13 0.088
142
TBR010 Tuberculosis 84 0.085
143
ANR008 Aneurysm Disease 57 0.085
144
PPL021 Papilledema 52 0.085
145
FTL044 Fetal Cytomegalovirus Syndrome 28 0.085
146
CRN019 Coronary Artery Vasospasm 26 0.085
147
TFT003 Tufting Enteropathy 21 0.085
148
FCT007 Factor Vii Deficiency 78 0.083
149
BRN024 Bronchitis 76 0.083
150
ACQ007 Acquired Immunodeficiency Syndrome 63 0.083
151
LGG001 Legg-Calve-Perthes Disease 61 0.083
152
SND002 Sneddon Syndrome 58 0.083
153
CRN020 Coronary Restenosis 50 0.083
154
P ENC008 Encephalocele 34 0.083
155
MNN021 Meningococcemia 32 0.083
156
NNS006 Non-Suppurative Otitis Media 26 0.083
157
P OBS005 Obesity 93 0.080
158
VNW001 Von Willebrand's Disease 74 0.080
159
c HMP007 Hemophilia 68 0.080
160
MYM001 Myoma 59 0.080
161
P CRV039 Cervicitis 52 0.080
162
P CRN074 Coronary Artery Aneurysm 34 0.080
163
CNG298 Congenital Pancreatic Cyst 12 0.080
164
PRT036 Peritonitis 78 0.076
165
DWN001 Down Syndrome 62 0.076
166
P MMB002 Membranous Glomerulonephritis 60 0.076
167
P ADN016 Adenocarcinoma 60 0.076
168
P RTN022 Retinal Vein Occlusion 59 0.076
169
PRT012 Prothrombin Deficiency 57 0.076
170
MYC002 Mycobacterium Avium Complex Disease 57 0.076
171
LYM019 Lymphosarcoma 54 0.076
172
c ESS003 Essential Thrombocythemia 50 0.076
173
c ALM001 Al Amyloidosis 44 0.076
174
FLM003 Fulminant Viral Hepatitis 28 0.076
175
THY020 Thyroid Hyalinizing Trabecular Adenoma 17 0.076
176
CYT018 Cytochrome P450 2d6 Variant 13 0.076
177
CGH002 Cough Headache 5 0.076
178
FCT001 Factor Viii Deficiency 71 0.073
179
P LVR013 Liver Disease 70 0.073
180
c HYD006 Hydrocephalus 70 0.073
181
P ANR007 Anorexia Nervosa 67 0.073
182
DFC004 Deficiency Anemia 66 0.073
183
P MLG002 Malignant Peritoneal Mesothelioma 55 0.073
184
P END033 Endocarditis 48 0.073
185
P APL006 Aplasia Cutis Congenita 47 0.073
186
P PNC102 Pancreatitis, Chronic 39 0.073
187
PST026 Postphlebitic Syndrome 32 0.073
188
HYP319 Hypereosinophilic Syndrome, Idiopathic, Resistant to Imatinib 31 0.073
189
c DBT009 Diabetes Mellitus 80 0.070
190
BHC002 Behcet's Disease 76 0.070
191
P MYL005 Myelofibrosis 75 0.070
192
BLR001 Biliary Atresia 67 0.070
193
CRB039 Cerebrovascular Disease 61 0.070
194
P HYP083 Hypopituitarism 58 0.070
195
APP008 Appendicitis 57 0.070
196
ATX019 Ataxia with Vitamin E Deficiency 55 0.070
197
c CNT016 Central Retinal Vein Occlusion 53 0.070
198
INT007 Intermediate Coronary Syndrome 53 0.070
199
NNT016 Neonatal Hemochromatosis 44 0.070
200
SYN053 Syndromic Diarrhea 42 0.070
201
P DYS026 Dysfibrinogenemia 41 0.070
202
SPL006 Splenic Infarction 37 0.070
203
SYN036 Syncope 35 0.070
204
ZYG002 Zygomycosis 28 0.070
205
CHR158 Charles Bonnet Syndrome 15 0.070
206
MCR033 Macrocephaly-Capillary Malformation 8 0.070
207
SCK003 Sickle Cell Anemia 73 0.066
208
c THL005 Thalassemia 68 0.066
209
P GLM007 Glomerulonephritis 66 0.066
210
P HRD011 Hereditary Spherocytosis 66 0.066
211
ART021 Arteriosclerosis 65 0.066
212
WST001 West Syndrome 64 0.066
213
GST009 Gastroschisis 63 0.066
214
P RNL014 Renal Cell Carcinoma 59 0.066
215
THY033 Thyrotoxicosis 58 0.066
216
c ACT134 Acute Liver Failure 57 0.066
217
HLL004 Hellp Syndrome 57 0.066
218
P LYM026 Lymphoblastic Leukemia 56 0.066
219
P INT030 Intracranial Aneurysm 56 0.066
220
ART004 Aortic Atherosclerosis 54 0.066
221
P DYS142 Dyskeratosis Congenita, Autosomal Recessive 4 52 0.066
222
ANG054 Angina Pectoris 52 0.066
223
c ACT076 Acute Myocarditis 49 0.066
224
MYL020 Myelomeningocele 47 0.066
225
RCR001 Recurrent Corneal Erosion 44 0.066
226
P ATX010 Ataxia Neuropathy Spectrum 44 0.066
227
ENT001 Enterocele 42 0.066
228
P MBS002 Moebius Syndrome 42 0.066
229
c TTL001 Total Internal Ophthalmoplegia 17 0.066
230
P BRS047 Breast Cancer 105 0.062
231
P ACT019 Acute Myeloid Leukemia 94 0.062
232
CDS001 Cadasil 92 0.062
233
GLN003 Glanzmann's Thrombasthenia 80 0.062
234
KWS002 Kawasaki Disease 74 0.062
235
P ANG001 Angelman Syndrome 70 0.062
236
ART019 Aortic Valve Stenosis 68 0.062
237
P NRL016 Neural Tube Defects 67 0.062
238
VSC011 Vasculitis 67 0.062
239
ECL001 Eclampsia 63 0.062
240
SCK005 Sickle Cell Disease 62 0.062
241
c MLG069 Malignant Hypertension 60 0.062
242
P CNG019 Congenital Afibrinogenemia 59 0.062
243
P THR090 Thrombocythemia 1 54 0.062
244
ANG011 Angiodysplasia 50 0.062
245
P CNT028 Central Retinal Artery Occlusion 49 0.062
246
c ACR001 Aicardi-Goutieres Syndrome 49 0.062
247
INF013 Inferior Myocardial Infarction 38 0.062
248
ABD004 Abdominal Tuberculosis 37 0.062
249
ACQ017 Acquired Von Willebrand Syndrome 36 0.062
250
MNT147 Mental Retardation 35 0.062
251
CRN185 Craniofacial Deafness Hand Syndrome 32 0.062
252
WRF001 Warfarin Resistance 31 0.062
253
CNG058 Congenital Antithrombin Deficiency Type 3 31 0.062
254
CRN220 Craniodiaphyseal Dysplasia, Autosomal Dominant 27 0.062
255
PRT015 Partial Third-Nerve Palsy 26 0.062
256
c HPT073 Hepatitis C Virus 25 0.062
257
MTH027 Mthfr Deficiency 24 0.062
258
PLM108 Pulmonary Interstitial Glycogenosis 14 0.062
259
MTH028 Mthfr Thermolabile Variant 13 0.062
260
c CRN172 Coronary Heart Disease 3 13 0.062
261
c CRN178 Coronary Heart Disease 6 12 0.062
262
EPT015 Epitheliopathy, Acute Posterior Multifocal Placoid Pigment 11 0.062
263
P ART022 Arthritis 75 0.058
264
GLL008 Gilles De La Tourette Syndrome 73 0.058
265
P HPT001 Hepatitis C 66 0.058
266
c HPT016 Hepatitis B 65 0.058
267
ART005 Arteriovenous Malformation 63 0.058
268
SRC014 Sarcoma 63 0.058
269
ART016 Aortic Aneurysm 62 0.058
270
CHL067 Cholecystitis 62 0.058
271
FCT002 Factor Xi Deficiency 62 0.058
272
c HYP076 Hyperthyroidism 61 0.058
273
P HMR003 Hemorrhagic Disease 59 0.058
274
HPT019 Hepatic Encephalopathy 58 0.058
275
MDS022 Mediastinitis 56 0.058
276
INT002 Intermittent Claudication 56 0.058
277
EGG001 Egg Allergy 54 0.058
278
PLC007 Placental Abruption 53 0.058
279
SVR005 Severe Pre-Eclampsia 52 0.058
280
INV001 Invasive Aspergillosis 49 0.058
281
HYD028 Hydrops, Ectopic Calcification, Moth-Eaten Skeletal Dysplasia 43 0.058
282
IMM020 Immunodeficiency with Hyper Igm Type 2 37 0.058
283
c SPH018 Spherocytosis, Hereditary, Type 5 36 0.058
284
SPH007 Sphenoid Sinusitis 35 0.058
285
CYT008 Cytomegalovirus Infection 34 0.058
286
MSM007 Mesomelic Dysplasia Kantaputra Type 34 0.058
287
P SLP004 Salpingo-Oophoritis 31 0.058
288
P MLR006 Male Reproductive Organ Cancer 23 0.058
289
c BNG076 Benign Exophthalmos Syndrome 21 0.058
290
ADS007 Aids, Rapid Progression to 21 0.058
291
c CRN173 Coronary Heart Disease 8 11 0.058
292
SNG003 Single Ventricular Heart 9 0.058
293
CRT056 Carotidynia 5 0.058
294
P APL001 Aplastic Anemia 83 0.054
295
P LPR003 Leprosy 78 0.054
296
P ACT074 Acute Lymphocytic Leukemia 77 0.054
297
c CHR065 Chronic Myeloid Leukemia 74 0.054
298
ASP006 Aspergillosis 73 0.054
299
c MYL006 Myeloid Leukemia 72 0.054
300
TKY001 Takayasu's Arteritis 72 0.054
301
ATM004 Autoimmune Thrombocytopenic Purpura 68 0.054
302
BRN106 Burns 64 0.054
303
FCT003 Factor X Deficiency 64 0.054
304
ART001 Arterial Tortuosity Syndrome 62 0.054
305
NRP001 Neuropathy 61 0.054
306
P ESN007 Eosinophilia 60 0.054
307
CHL069 Cholesteatoma 58 0.054
308
CRY005 Cryptococcosis 57 0.054
309
c THR005 Thrombotic Thrombocytopenic Purpura 57 0.054
310
HYP063 Hypersplenism 56 0.054
311
VNS003 Venous Insufficiency 54 0.054
312
OPT009 Optic Neuritis 53 0.054
313
CRD001 Cardiac Tamponade 52 0.054
314
PTR001 Petrositis 51 0.054
315
P CMP008 Compartment Syndrome 51 0.054
316
HPT032 Hepatocellular Carcinoma, Somatic 50 0.054
317
P PND001 Pain Disorder 49 0.054
318
RTN021 Retinal Vascular Occlusion 49 0.054
319
FCL012 Facial Paralysis 49 0.054
320
ENT015 Enthesitis-Related Arthritis 48 0.054
321
MNN014 Mononeuritis 48 0.054
322
FCT005 Factor Xiii Deficiency 45 0.054
323
LPS007 Lupus Nephritis 43 0.054
324
AND003 Andersen-Tawil Syndrome 43 0.054
325
HDC001 Headache 43 0.054
326
VTM001 Vitamin K Deficiency Hemorrhagic Disease 42 0.054
327
c TWN006 Twin Twin Transfusion Syndrome 40 0.054
328
CMB021 Combined Pituitary Hormone Deficiency 40 0.054
329
P SNS014 Sinusitis 40 0.054
330
ACT099 Acute Fatty Liver of Pregnancy 39 0.054
331
P PRV002 Periventricular Nodular Heterotopia 39 0.054
332
RFR010 Refractory Anemia 39 0.054
333
NNT020 Neonatal Intrahepatic Cholestasis Caused by Citrin Deficiency 38 0.054
334
P MYH004 Myh9 Related Thrombocytopenia 37 0.054
335
P JVN024 Juvenile Hereditary Hemochromatosis 35 0.054
336
FTL012 Fetal and Neonatal Alloimmune Thrombocytopenia 32 0.054
337
c FRN011 Frontal Sinusitis 32 0.054
338
PRT045 Prothrombin-Related Thrombophilia 31 0.054
339
RTR011 Retroperitoneal Fibrosis 31 0.054
340
FRN014 Fournier Gangrene 30 0.054
341
SCR024 Sacrococcygeal Teratoma 30 0.054
342
SPN185 Spinal Cord Infarction 30 0.054
343
SBD001 Subdural Empyema 29 0.054
344
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.054
345
ENC017 Encephaloceles 26 0.054
346
GRF006 Grfoma 26 0.054
347
c HMP017 Hemophilia a, Congenital 21 0.054
348
AND005 Androgen Insensitivity Syndrome, Mild 18 0.054
349
c CRN174 Coronary Heart Disease 2 17 0.054
350
THN005 Thunderclap Headache 7 0.054
351
P ALZ001 Alzheimer's Disease 103 0.049
352
P PHC003 Pheochromocytoma 81 0.049
353
P PNM007 Pneumonia 79 0.049
354
P ALP006 Alpha Thalassemia 75 0.049
355
P ABD003 Abdominal Aortic Aneurysm 71 0.049
356
c BTT002 Beta Thalassemia 70 0.049
357
DBT001 Diabetic Ketoacidosis 69 0.049
358
P CLN016 Colon Cancer 67 0.049
359
c VRL010 Viral Hepatitis 61 0.049
360
P BRN019 Bernard-Soulier Syndrome 59 0.049
361
OST017 Osteomyelitis 59 0.049
362
P PYL005 Pyelonephritis 57 0.049
363
P SPH001 Sapho Syndrome 56 0.049
364
PLV003 Pelvic Inflammatory Disease 56 0.049
365
P MTR012 Mitral Valve Disease 56 0.049
366
PRP007 Priapism 55 0.049
367
ANR004 Anuria 55 0.049
368
c EPS003 Episodic Ataxia 55 0.049
369
PRR002 Pure Red-Cell Aplasia 54 0.049
370
c INT070 Intestinal Obstruction 54 0.049
371
P LBY004 Labyrinthitis 53 0.049
372
CRN030 Coronary Stenosis 53 0.049
373
P HRD057 Hereditary Pancreatitis 53 0.049
374
CCN002 Cocaine Abuse 53 0.049
375
MYL001 Myelitis 52 0.049
376
P EXP004 Exophthalmos 51 0.049
377
HMR002 Hemarthrosis 50 0.049
378
TRC023 Trichinosis 48 0.049
379
RDC002 Radiculopathy 48 0.049
380
PRT019 Protein-Losing Enteropathy 48 0.049
381
ETH009 Ethmoid Sinusitis 44 0.049
382
ERY004 Erysipelas 43 0.049
383
GNT031 Genitopatellar Syndrome 42 0.049
384
CDQ001 Cauda Equina Syndrome 40 0.049
385
TYP013 Type 1 Von Willebrand Disease 40 0.049
386
LCK001 Locked-in Syndrome 39 0.049
387
P WRF002 Warfarin Sensitivity 39 0.049
388
c CRT018 Carotid Intimal Medial Thickness 37 0.049
389
HDN002 Head Injury 36 0.049
390
WBR001 Weber Syndrome 33 0.049
391
GNT005 Giant Hemangioma 28 0.049
392
AMR003 Amaurosis Fugax 28 0.049
393
SHW001 Shwartzman Phenomenon 23 0.049
394
HNS001 Hansen's Disease 22 0.049
395
P OCL041 Oculomotor Apraxia Cogan Type 18 0.049
396
HRD083 Hereditary Antithrombin Deficiency 16 0.049
397
c THR023 Thrombophilia Due to Thrombomodulin Defect 16 0.049
398
c OPT031 Optic Neuropathy, Anterior Ischemic 13 0.049
399
HDG007 Hodgkin's Lymphoma 91 0.044
400
AND002 Androgen Insensitivity Syndrome 88 0.044
401
P FML021 Familial Hypercholesterolemia 87 0.044
402
BRK003 Burkitt's Lymphoma 78 0.044
403
P TRN020 Turner Syndrome 77 0.044
404
TTR001 Tetralogy of Fallot 76 0.044
405
P WGN002 Wegener's Granulomatosis 75 0.044
406
P FML018 Familial Mediterranean Fever 74 0.044
407
P LNG032 Lung Cancer 74 0.044
408
P TMP003 Temporal Arteritis 69 0.044
409
P MLG075 Malignant Mesothelioma 69 0.044
410
MRB003 Morbid Obesity 68 0.044
411
c HYP086 Hypothyroidism 68 0.044
412
KLN001 Klinefelter's Syndrome 67 0.044
413
TRP002 Tropical Spastic Paraparesis 67 0.044
414
HYP066 Hyperglycemia 65 0.044
415
P MLN008 Melanoma 65 0.044
416
NRN002 Neuronitis 64 0.044
417
CRB037 Cerebral Palsy 64 0.044
418
ADR015 Adrenocortical Carcinoma 63 0.044
419
TYP007 Typhoid Fever 63 0.044
420
P LMY004 Leiomyosarcoma 62 0.044
421
PHR003 Pharyngitis 62 0.044
422
DDN006 Duodenitis 62 0.044
423
PRS047 Prostatitis 62 0.044
424
P INT068 Intestinal Disease 61 0.044
425
P CNJ013 Conjunctivitis 61 0.044
426
RNL015 Renal Hypertension 60 0.044
427
c AXN002 Axenfeld-Rieger Syndrome 60 0.044
428
P ESP024 Esophagitis 60 0.044
429
CHR001 Churg-Strauss Syndrome 59 0.044
430
c MYL007 Myeloma 59 0.044
431
c MST009 Mastocytosis 59 0.044
432
ASP003 Aseptic Meningitis 58 0.044
433
c HPT015 Hepatitis D 57 0.044
434
c HYP095 Hypercholesterolemia 56 0.044
435
END031 Endometrial Stromal Sarcoma 56 0.044
436
P CHR092 Chronic Myeloproliferative Disease 55 0.044
437
CVR006 Cavernous Hemangioma 54 0.044
438
EXS001 Exostosis 54 0.044
439
CRN029 Coronary Arteriosclerosis 53 0.044
440
ADL002 Adult Syndrome 52 0.044
441
P BLD034 Bile Duct Carcinoma 52 0.044
442
c ACT042 Acute Pyelonephritis 52 0.044
443
GRY002 Gray Platelet Syndrome 51 0.044
444
VRC001 Varicocele 51 0.044
445
CHL004 Cholelithiasis 51 0.044
446
NRT004 Neuritis 51 0.044
447
CNV002 Conversion Disorder 50 0.044
448
CRB004 Cerebral Artery Occlusion 47 0.044
449
c BNG032 Benign Mesothelioma 46 0.044
450
HPT008 Hepatic Tuberculosis 45 0.044
451
CRT012 Cortical Blindness 45 0.044
452
ACT055 Actinomycosis 42 0.044
453
LPD004 Lipoid Nephrosis 42 0.044
454
BNS003 Binswanger's Disease 40 0.044
455
c MYL014 Myeloproliferative Disorder 39 0.044
456
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 39 0.044
457
PRS021 Prostatic Adenoma 38 0.044
458
SCT005 Scott Syndrome 38 0.044
459
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 37 0.044
460
BCT015 Bacteremia 37 0.044
461
SPL018 Splenomegaly 37 0.044
462
SCR015 Scarlet Fever 36 0.044
463
RHS001 Rh Isoimmunization 35 0.044
464
MGL023 Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome, Somatic 33 0.044
465
LKM059 Leukemia, Megakaryoblastic, with or Without Down Syndrome, Somatic 33 0.044
466
PTL001 Patulous Eustachian Tube 30 0.044
467
TYP015 Type 2b Von Willebrand Disease 28 0.044
468
RHB020 Rhabdomyosarcoma, Somatic 27 0.044
469
BNM005 Bone Marrow Necrosis 27 0.044
470
BSL004 Basilar Artery Occlusion 27 0.044
471
P HYP078 Hypertrophy of Breast 26 0.044
472
c ACT036 Acute Cholangitis 25 0.044
473
HNM002 Hinman Syndrome 24 0.044
474
PL2001 Pla2g6-Associated Neurodegeneration 21 0.044
475
PTT043 Pituitary Hormone Deficiency, Combined, 6 17 0.044
476
BNT001 Banti's Syndrome 8 0.044
477
P TBR001 Tuberous Sclerosis 91 0.038
478
P MLT019 Multiple Myeloma 89 0.038
479
P RTT002 Rett Syndrome 85 0.038
480
P MLT020 Multiple Sclerosis 82 0.038
481
P PRM021 Primary Pulmonary Hypertension 82 0.038
482
P MNN012 Meningioma 79 0.038
483
c TYP008 Type 1 Diabetes Mellitus 77 0.038
484
PRP027 Peripheral Vascular Disease 75 0.038
485
SCH014 Schistosomiasis 72 0.038
486
P HML002 Hemolytic Anemia 68 0.038
487
KLP002 Klippel-Trenaunay Syndrome 67 0.038
488
c THY032 Thyroiditis 67 0.038
489
GSG001 Gas Gangrene 66 0.038
490
HYP056 Hypoglycemia 66 0.038
491
P CMP010 Complex Regional Pain Syndrome 65 0.038
492
c ENC004 Encephalitis 64 0.038
493
AMN001 Amenorrhea 63 0.038
494
P GRV001 Graves' Disease 63 0.038
495
CRN036 Craniopharyngioma 62 0.038
496
TNS005 Tonsillitis 62 0.038
497
PPT003 Peptic Ulcer 61 0.038
498
P HYP080 Hypogonadism 60 0.038
499
CRT049 Critical Limb Ischemia 60 0.038
500
SPT004 Septic Arthritis 60 0.038
501
CHR074 Choriocarcinoma 59 0.038
502
LYM021 Lymphadenitis 58 0.038
503
c KDN018 Kidney Disease 58 0.038
504
P RNV001 Renovascular Hypertension 58 0.038
505
PRC013 Pericarditis 57 0.038
506
URM002 Uremia 56 0.038
507
HST009 Histiocytoma 56 0.038
508
P LYM025 Lymphedema 56 0.038
509
P END047 Endophthalmitis 56 0.038
510
CRV031 Cervical Adenocarcinoma 56 0.038
511
P MYM002 Moyamoya Disease 56 0.038
512
STS002 Situs Inversus 56 0.038
513
NPH011 Nephroblastoma 56 0.038
514
P BRN009 Burning Mouth Syndrome 56 0.038
515
P PNC001 Pancytopenia 55 0.038
516
ANG018 Angiomyolipoma 54 0.038
517
P HML001 Hemolytic-Uremic Syndrome 54 0.038
518
RHB003 Rhabdomyosarcoma 54 0.038
519
PRC012 Pericardial Effusion 54 0.038
520
CLL002 Collecting Duct Carcinoma 54 0.038
521
P HYP273 Hypothyroidism, Congenital, Due to Thyroid Dysgenesis or Hypoplasia 54 0.038
522
c CTR002 Cataract 53 0.038
523
SPN035 Spindle Cell Sarcoma 53 0.038
524
c OPH004 Ophthalmoplegia 52 0.038
525
THY089 Thymic Epithelial Neoplasm 52 0.038
526
VTM002 Vitamin B12 Deficiency 51 0.038
527
LNG029 Lung Adenocarcinoma 49 0.038
528
PRP016 Paraplegia 48 0.038
529
CRD137 Cardiogenic Shock 47 0.038
530
P HMG003 Hemoglobin E Disease 42 0.038
531
END021 Endomyocardial Fibrosis 42 0.038
532
EPD005 Epidural Abscess 39 0.038
533
c CRB126 Cerebral Cavernous Malformation 39 0.038
534
PLS018 Plasminogen Activator Inhibitor Type 1 Deficiency 38 0.038
535
HNC001 Henoch-Schoenlein Purpura 38 0.038
536
c BLN003 Blindness 37 0.038
537
INF058 Inflammatory Myofibroblastic Tumor 37 0.038
538
EMN001 Emanuel Syndrome 36 0.038
539
P DPH016 Diaphragmatic Hernia 3 36 0.038
540
PTT021 Pituitary Hormone Deficiency, Combined 2 36 0.038
541
c SBC003 Subacute Bacterial Endocarditis 35 0.038
542
CTR003 Citrin Deficiency 35 0.038
543
MTR001 Mature Cataract 34 0.038
544
ORB013 Orbital Disease 32 0.038
545
DYS036 Dysequilibrium Syndrome 28 0.038
546
THR089 Thrombophilia Due to Protein S Deficiency, Autosomal Dominant 27 0.038
547
DFN039 Deafness-Infertility Syndrome 27 0.038
548
CRT045 Creatine Phosphokinase, Elevated Serum 26 0.038
549
P PRX010 Paroxysmal Ventricular Fibrillation 22 0.038
550
P KRN003 Kernicterus Due to Isoimmunization 21 0.038
551
INF001 Infarct of Liver 20 0.038
552
CRB031 Cerebral Arterial Disease 19 0.038
553
HMC030 Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency 17 0.038
554
P ISC010 Isochromosome Yp 14 0.038
555
NNT025 Neonatal Systemic Lupus Erythematosus 14 0.038
556
CVR001 Cavernous Sinus Meningioma 14 0.038
557
PRN017 Perianal Hematoma 13 0.038
558
c CRN175 Coronary Heart Disease 4 11 0.038
559
P PNC035 Pancreatic Cancer 95 0.031
560
GLC006 Galactosemia 93 0.031
561
P FML011 Familial Adenomatous Polyposis 93 0.031
562
P RHM011 Rheumatoid Arthritis 91 0.031
563
P WSK001 Wiskott-Aldrich Syndrome 87 0.031
564
P MDL005 Medulloblastoma 82 0.031
565
P OVR042 Ovarian Cancer 79 0.031
566
OBS002 Obsessive-Compulsive Disorder 73 0.031
567
CHL065 Cholangiocarcinoma 73 0.031
568
P CLC005 Celiac Disease 73 0.031
569
P AST007 Astrocytoma 72 0.031
570
c ESS002 Essential Hypertension 71 0.031
571
LKC001 Leukocyte Adhesion Deficiency 70 0.031
572
SPN038 Spina Bifida 70 0.031
573
OLL001 Ollier Disease 70 0.031
574
P SYS004 Systemic Mastocytosis 70 0.031
575
P END044 Endometriosis 69 0.031
576
ISC006 Ischemic Heart Disease 69 0.031
577
ADL030 Adult-Onset Still's Disease 68 0.031
578
P HMN010 Hemangioma 68 0.031
579
IRR002 Irritable Bowel Syndrome 68 0.031
580
DRM006 Dermatitis 68 0.031
581
PMS001 Poems Syndrome 67 0.031
582
P PLY014 Polycystic Kidney Disease 67 0.031
583
ADN018 Adenoma 67 0.031
584
GNG013 Gingivitis 67 0.031
585
P PRD008 Periodontitis 66 0.031
586
MLG056 Malignant Hyperthermia 65 0.031
587
P STM004 Stomach Cancer 65 0.031
588
DBN001 Dubin-Johnson Syndrome 64 0.031
589
ARG002 Argininosuccinic Aciduria 64 0.031
590
STS003 Sitosterolemia 64 0.031
591
CYS005 Cysticercosis 64 0.031
592
P DYS007 Dyskeratosis Congenita 64 0.031
593
TXC005 Toxic Shock Syndrome 63 0.031
594
GLC003 Glucose Intolerance 63 0.031
595
c CHR090 Chronic Lymphocytic Leukemia 63 0.031
596
P OST009 Osteochondritis Dissecans 62 0.031
597
c MSC005 Muscular Dystrophy 62 0.031
598
BRN029 Brain Disease 62 0.031
599
P ANP001 Anaplastic Large Cell Lymphoma 61 0.031
600
CRY004 Cryoglobulinemia 61 0.031
601
NRN004 Neuroendocrine Tumor 61 0.031
602
c EHL001 Ehlers-Danlos Syndrome 61 0.031
603
P LPS002 Liposarcoma 61 0.031
604
c CNT035 Central Nervous System Disease 60 0.031
605
MLT001 Multiple Chemical Sensitivity 59 0.031
606
P CLL015 Collagen Disease 59 0.031
607
ACR008 Acrocallosal Syndrome 59 0.031
608
P RBL001 Rubella 59 0.031
609
ARR001 Arrhythmogenic Right Ventricular Dysplasia 59 0.031
610
CRT016 Carotid Artery Disease 58 0.031
611
c ATM010 Autoimmune Hemolytic Anemia 57 0.031
612
HNT002 Hantavirus Pulmonary Syndrome 57 0.031
613
P DBT005 Diabetes Insipidus 57 0.031
614
BRN004 Brain Edema 57 0.031
615
CNN005 Connective Tissue Disease 57 0.031
616
ANT011 Antisocial Personality Disorder 57 0.031
617
PYD001 Pyoderma Gangrenosum 57 0.031
618
P CHL066 Cholangitis 57 0.031
619
PRT039 Proteinuria 57 0.031
620
MGC001 Megacolon 56 0.031
621
P MYC008 Myocarditis 56 0.031
622
P SYR001 Syringomyelia 55 0.031
623
ACT017 Acute Chest Syndrome 55 0.031
624
PNH001 Panhypopituitarism 55 0.031
625
c CNG015 Congenital Diaphragmatic Hernia 55 0.031
626
c BCT007 Bacterial Meningitis 54 0.031
627
VGN023 Vaginitis 54 0.031
628
P HYP098 Hypereosinophilic Syndrome 54 0.031
629
c DRR001 Diarrhea 54 0.031
630
HMP005 Hemiplegia 54 0.031
631
CHC001 Chickenpox 54 0.031
632
ALX001 Alexia 54 0.031
633
TRN007 Transsexualism 53 0.031
634
DNG001 Dengue Shock Syndrome 53 0.031
635
NRR001 Neuroretinitis 52 0.031
636
CRT013 Carotid Stenosis 51 0.031
637
P ALV004 Alveolar Rhabdomyosarcoma 51 0.031
638
OBS001 Obstructive Jaundice 51 0.031
639
P LCT002 Lactose Intolerance 50 0.031
640
STT004 Steatorrhea 50 0.031
641
FSC004 Fasciitis 50 0.031
642
IRN002 Iron Metabolism Disease 50 0.031
643
PLM010 Pulmonary Edema 50 0.031
644
PYD002 Pyoderma 49 0.031
645
URT010 Ureteral Obstruction 49 0.031
646
c HYD002 Hydronephrosis 48 0.031
647
GST040 Gastric Adenocarcinoma 48 0.031
648
SMN007 Seminoma 48 0.031
649
ACT095 Acute Biphenotypic Leukemia 47 0.031
650
CRN014 Cronkhite-Canada Syndrome 46 0.031
651
LYM014 Lymphangitis 46 0.031
652
PNC033 Pancreas Adenocarcinoma 46 0.031
653
LYM020 Lymph Node Cancer 45 0.031
654
PRS045 Prostatic Hypertrophy 44 0.031
655
PRT093 Proteus Syndrome, Somatic 44 0.031
656
PLR007 Pleural Empyema 44 0.031
657
INT079 Intrahepatic Cholangiocarcinoma 43 0.031
658
P CRN157 Coronary Heart Disease 43 0.031
659
CRT008 Carotid Artery Dissection 42 0.031
660
LYM012 Lymphoplasmacytic Lymphoma 42 0.031
661
LYM040 Lymphoblastic Lymphoma 42 0.031
662
MYS004 Myiasis 42 0.031
663
TRN012 Transient Global Amnesia 42 0.031
664
c CRN035 Cranial Nerve Palsy 41 0.031
665
PRM008 Parametritis 41 0.031
666
OBS004 Obstructive Hydrocephalus 41 0.031
667
WTH001 Withdrawal Disorder 40 0.031
668
P HRN001 Horner's Syndrome 40 0.031
669
P HMR005 Hemorrhoid 39 0.031
670
QBC001 Quebec Platelet Disorder 39 0.031
671
PRL008 Paralytic Ileus 39 0.031
672
NPH051 Nephritis 39 0.031
673
IPX001 Ipex Syndrome 39 0.031
674
TXC012 Toxic Epidermal Necrolysis 38 0.031
675
RBF001 Riboflavin Deficiency 38 0.031
676
c ERY013 Erythrocytosis 37 0.031
677
ESP002 Esophageal Varix 37 0.031
678
VRC005 Varicose Veins 37 0.031
679
P CHR038 Chronic Maxillary Sinusitis 37 0.031
680
P CST002 Castleman's Disease 37 0.031
681
VRL011 Viral Infectious Disease 37 0.031
682
HMC020 Homocystinuria, B6-Responsive and Nonresponsive Types 35 0.031
683
ALP044 Alpha-1-Antichymotrypsin Deficiency 33 0.031
684
LYM005 Lymphocele 33 0.031
685
CRB088 Cerebral Atrophy 33 0.031
686
CHY006 Chylous Ascites 30 0.031
687
TXC001 Toxic Megacolon 29 0.031
688
THR067 Thrombophilia Due to Protein C Deficiency, Autosomal Dominant 29 0.031
689
ART007 Aorta Atresia 27 0.031
690
P MLD013 Mild Hemophilia a 27 0.031
691
ISC001 Ischemic Neuropathy 26 0.031
692
ADT003 Auditory System Disease 26 0.031
693
P MLT009 Multiple Cranial Nerve Palsy 24 0.031
694
TYP016 Type 2m Von Willebrand Disease 23 0.031
695
TYP017 Type 2n Von Willebrand Disease 23 0.031
696
TYP014 Type 2a Von Willebrand Disease 23 0.031
697
ANG022 Angel Shaped Phalangoepiphyseal Dysplasia 22 0.031
698
c ACT035 Acute Frontal Sinusitis 21 0.031
699
c MLD014 Mild Hemophilia B 21 0.031
700
RHM007 Rheumatic Congestive Heart Failure 21 0.031
701
c SVR057 Severe Hemophilia B 20 0.031
702
PLS001 Pulsating Exophthalmos 20 0.031
703
MLT037 Multifocal Lymphangioendotheliomatosis with Thrombocytopenia 19 0.031
704
CNT059 Central Post-Stroke Pain 19 0.031
705
CHR176 Chromophil Renal Cell Carcinoma 18 0.031
706
THR007 Thrombophlebitis Migrans 18 0.031
707
LGP003 Logopenic Progressive Aphasia 18 0.031
708
ADS005 Aids Dysmorphic Syndrome 17 0.031
709
MNN005 Meningovascular Neurosyphilis 17 0.031
710
3Q2002 3q21q26 Syndrome 16 0.031
711
c ACT061 Acute Sphenoidal Sinusitis 16 0.031
712
HGH021 Hughes-Stovin Syndrome 14 0.031
713
SGM001 Sigmoid Disease 14 0.031
714
CMV001 Cmv Antenatal Infection 13 0.031
715
OTP003 Oto-Palatal-Digital Syndrome 13 0.031
716
MGL021 Megalencephaly-Capillary Malformation Syndrome 13 0.031
717
VSC010 Vascular Tissue Disease 12 0.031
718
THR088 Thrombophilia Due to Protein S Deficiency, Autosomal Recessive 8 0.031
719
ACT174 Acute Peripheral Arterial Occlusion 2 0.031
720
CYS001 Cystic Fibrosis 103 0.022
721
P TYP009 Type 2 Diabetes Mellitus 93 0.022
722
P LFR001 Li-Fraumeni Syndrome 93 0.022
723
P PRK002 Parkinson's Disease 92 0.022
724
FBR012 Fabry Disease 88 0.022
725
P HRD008 Hereditary Hemorrhagic Telangiectasia 86 0.022
726
SVR004 Severe Combined Immunodeficiency 85 0.022
727
AGR001 Age Related Macular Degeneration 83 0.022
728
PTZ001 Peutz-Jeghers Syndrome 83 0.022
729
P DLT002 Dilated Cardiomyopathy 82 0.022
730
CNG034 Congestive Heart Failure 81 0.022
731
P HMC003 Hemochromatosis 80 0.022
732
P RBN001 Rubinstein-Taybi Syndrome 78 0.022
733
ACT033 Acute Intermittent Porphyria 78 0.022
734
DCH001 Duchenne Muscular Dystrophy 78 0.022
735
RNL002 Renal Agenesis 77 0.022
736
CRB011 Cerebrotendinous Xanthomatosis 77 0.022
737
P LYM007 Lymphangioleiomyomatosis 74 0.022
738
P PRD006 Prader-Willi Syndrome 74 0.022
739
P PRM006 Primary Biliary Cirrhosis 74 0.022
740
P CLR023 Colorectal Cancer 73 0.022
741
P CNG026 Congenital Heart Defect 73 0.022
742
P MLR004 Malaria 73 0.022
743
GST023 Gastric Ulcer 72 0.022
744
NNH001 Non-Hodgkin Lymphoma 72 0.022
745
P NRB001 Neuroblastoma 71 0.022
746
P MGR002 Migraine 71 0.022
747
P ATM003 Autoimmune Thyroiditis 70 0.022
748
c OST005 Osteogenesis Imperfecta 70 0.022
749
BCK001 Becker Muscular Dystrophy 69 0.022
750
P TYP020 Type 1 Diabetes 69 0.022
751
P INF038 Influenza 69 0.022
752
c SRC013 Sarcoidosis 69 0.022
753
CCC001 Coccidioidomycosis 68 0.022
754
LMY002 Leiomyoma 68 0.022
755
c PRM002 Primary Hyperoxaluria 68 0.022
756
PLY017 Polyarteritis Nodosa 68 0.022
757
P GST044 Gastritis 68 0.022
758
P ATP001 Atopic Dermatitis 68 0.022
759
P DDN001 Duodenal Ulcer 68 0.022
760
DBT010 Diabetic Neuropathy 68 0.022
761
P PLY011 Polycystic Ovary Syndrome 68 0.022
762
P RTH001 Rothmund-Thomson Syndrome 67 0.022
763
BRN028 Brain Cancer 67 0.022
764
MYS005 Myositis 67 0.022
765
P UVT001 Uveitis 67 0.022
766
P OLG002 Oligodendroglioma 67 0.022
767
STT001 Status Epilepticus 66 0.022
768
CRB042 Cerebellar Ataxia 66 0.022
769
P KDN017 Kidney Cancer 66 0.022
770
P PLM036 Pulmonary Fibrosis 66 0.022
771
P ART023 Arthropathy 66 0.022
772
ACT010 Acth-Secreting Pituitary Adenoma 66 0.022
773
P AMY004 Amyloidosis 65 0.022
774
MXD005 Mixed Connective Tissue Disease 65 0.022
775
P PRM124 Primary Hyperoxaluria Type 1 65 0.022
776
MLD001 Melioidosis 65 0.022
777
P MLG077 Malignant Peripheral Nerve Sheath Tumor 64 0.022
778
GLB015 Glioblastoma Multiforme 64 0.022
779
c OST026 Osteogenesis Imperfecta Type I 64 0.022
780
CCT002 Cicatricial Pemphigoid 64 0.022
781
c PRP029 Porphyria 64 0.022
782
MYL040 Myelodysplastic Syndromes 64 0.022
783
PTT006 Pituitary Adenoma 64 0.022
784
CHL068 Cholestasis 63 0.022
785
BRC012 Brucellosis 63 0.022
786
PLS011 Plasmacytoma 63 0.022
787
NTH001 Netherton Syndrome 63 0.022
788
ECH003 Echinococcosis 63 0.022
789
PLM001 Pulmonary Tuberculosis 63 0.022
790
P CHN012 Chondrosarcoma 63 0.022
791
P OVR049 Ovarian Disease 63 0.022
792
c SPN046 Spinal Muscular Atrophy 63 0.022
793
P CRV035 Cervical Cancer 62 0.022
794
LPR001 Lepromatous Leprosy 62 0.022
795
BLM002 Bulimia Nervosa 62 0.022
796
ERY008 Erythromelalgia 62 0.022
797
PLS006 Plasmodium Vivax Malaria 62 0.022
798
SMT015 Smith Magenis Syndrome 62 0.022
799
P GTR002 Goiter 61 0.022
800
P ACT009 Acute Monocytic Leukemia 61 0.022
801
FTT001 Fatty Liver Disease 61 0.022
802
P CNG042 Congenital Central Hypoventilation Syndrome 61 0.022
803
c DMN001 Diamond-Blackfan Anemia 61 0.022
804
P NRV007 Nervous System Disease 61 0.022
805
c HYP061 Hypertrophic Cardiomyopathy 61 0.022
806
CHL014 Cholera 61 0.022
807
ADN002 Adenoiditis 60 0.022
808
RTN025 Retinoschisis 60 0.022
809
PSR002 Psoriasis 60 0.022
810
FDL002 Food Allergy 60 0.022
811
ACT049 Acute Disseminated Encephalomyelitis 60 0.022
812
ACS001 Acoustic Neuroma 60 0.022
813
SCR008 Scrub Typhus 59 0.022
814
INT051 Intussusception 59 0.022
815
CRB021 Cerebral Malaria 59 0.022
816
ALV005 Alveolar Soft Part Sarcoma 59 0.022
817
c MNC007 Monocytic Leukemia 59 0.022
818
c FML035 Familial Hyperlipidemia 59 0.022
819
c SCL016 Scleroderma 59 0.022
820
CMP002 Campylobacteriosis 59 0.022
821
P HMN013 Hemangiopericytoma 58 0.022
822
P RNL007 Renal Tubular Acidosis 58 0.022
823
P GLC007 Glaucoma 58 0.022
824
P TWN001 Twin-to-Twin Transfusion Syndrome 58 0.022
825
TYP011 Typhus 58 0.022
826
BBS001 Babesiosis 58 0.022
827
RTN018 Retinal Disease 58 0.022
828
DNG003 Dengue Disease 58 0.022
829
ADN011 Adenoid Cystic Carcinoma 58 0.022
830
NRN001 Neuroendocrine Carcinoma 57 0.022
831
c HRM001 Hermansky-Pudlak Syndrome 57 0.022
832
GST037 Gastroparesis 57 0.022
833
SRS001 Serous Cystadenocarcinoma 57 0.022
834
HRD012 Hereditary Elliptocytosis 57 0.022
835
MTN003 Motion Sickness 57 0.022
836
NPH010 Nephrosclerosis 56 0.022
837
BLL003 Bell's Palsy 56 0.022
838
P DND001 Dandy-Walker Syndrome 56 0.022
839
PRT029 Parathyroid Adenoma 56 0.022
840
CRT002 Cartilage-Hair Hypoplasia 56 0.022
841
P SYP003 Syphilis 56 0.022
842
MCN001 Mucinous Adenocarcinoma 56 0.022
843
PYR013 Pyruvate Kinase Deficiency 56 0.022
844
c THR003 Thoracic Aortic Aneurysm 56 0.022
845
GST027 Gastric Lymphoma 56 0.022
846
JPN002 Japanese Encephalitis 55 0.022
847
SPR004 Supravalvular Aortic Stenosis 55 0.022
848
FBR003 Fibrous Histiocytoma 55 0.022
849
SHR001 Short Bowel Syndrome 55 0.022
850
TRN015 Transient Cerebral Ischemia 55 0.022
851
XNT003 Xanthomatosis 55 0.022
852
NRL005 Neurilemmoma 55 0.022
853
CRN027 Corneal Neovascularization 55 0.022
854
ACT119 Acute Promyelocytic Leukemia 55 0.022
855
BNF002 Bone Fracture 55 0.022
856
ALC009 Alcoholic Liver Cirrhosis 55 0.022
857
LGN002 Legionellosis 55 0.022
858
P ANG015 Angioedema 54 0.022
859
P PLY006 Polydactyly 54 0.022
860
c DNT011 Dentinogenesis Imperfecta 54 0.022
861
KMR001 Kimura Disease 54 0.022
862
ART017 Aortic Disease 54 0.022
863
PLY041 Polymyositis 54 0.022
864
CLN019 Colonic Disease 54 0.022
865
HPT014 Hepatorenal Syndrome 54 0.022
866
DBT008 Diabetic Angiopathy 54 0.022
867
MLB002 Male Breast Cancer 54 0.022
868
c VNT002 Ventricular Septal Defect 53 0.022
869
c PST005 Posterior Uveitis 53 0.022
870
MCR088 Microscopic Polyangiitis 53 0.022
871
PNN001 Panniculitis 53 0.022
872
CNG048 Congenital Hepatic Fibrosis 53 0.022
873
SPL004 Splenic Marginal Zone Lymphoma 53 0.022
874
SDR002 Siderosis 53 0.022
875
MLL005 Miller-Dieker Syndrome 52 0.022
876
MCN007 Meconium Aspiration Syndrome 52 0.022
877
PRN011 Pernicious Anemia 52 0.022
878
CYS014 Cystadenocarcinoma 52 0.022
879
CLC001 Calciphylaxis 52 0.022
880
CHL061 Childhood Leukemia 52 0.022
881
GST060 Gastric Cancer, Somatic 52 0.022
882
EBS001 Ebstein Anomaly 52 0.022
883
P MSC003 Muscular Atrophy 52 0.022
884
P INT063 Intellectual Disability 51 0.022
885
SYN006 Synovial Sarcoma 51 0.022
886
PTT004 Pituitary Apoplexy 51 0.022
887
MDD002 Middle Ear Cholesteatoma 51 0.022
888
BRK001 Brooke-Spiegler Syndrome 51 0.022
889
CYS009 Cystadenoma 51 0.022
890
ANK001 Ankylosis 50 0.022
891
MNN009 Meningoencephalitis 50 0.022
892
P ATR005 Atrophic Gastritis 50 0.022
893
P OVR046 Ovarian Cyst 50 0.022
894
SCN036 Secondary Progressive Multiple Sclerosis 50 0.022
895
BRN032 Brain Glioma 50 0.022
896
KLT001 Klatskin's Tumor 50 0.022
897
MCL003 Macular Holes 50 0.022
898
LMY003 Leiomyomatosis 49 0.022
899
PRG008 Paragonimiasis 49 0.022
900
SPR016 Spermatic Cord Torsion 49 0.022
901
c APH002 Aphasia 49 0.022
902
SCR002 Scurvy 49 0.022
903
UTR039 Uterine Fibroid 49 0.022
904
UTR024 Uterine Carcinosarcoma 49 0.022
905
MYC005 Myocardial Stunning 49 0.022
906
END020 Endocardial Fibroelastosis 49 0.022
907
c ACT078 Acute Porphyria 48 0.022
908
CLN015 Colon Adenocarcinoma 48 0.022
909
PLY024 Polymicrogyria 48 0.022
910
LGN001 Legionnaires' Disease 48 0.022
911
ALC005 Alcoholic Pancreatitis 47 0.022
912
PYM001 Pyomyositis 47 0.022
913
c PSD003 Pseudohypoaldosteronism 47 0.022
914
RTN001 Retinal Vasculitis 47 0.022
915
P BCL006 B-Cell Lymphomas 47 0.022
916
c RST002 Restrictive Cardiomyopathy 47 0.022
917
IMP002 Imperforate Anus 47 0.022
918
c TYP002 Type Vi Ehlers-Danlos Syndrome 47 0.022
919
c HYP011 Hyperlipoproteinemia Type Iii 47 0.022
920
PRT026 Parotitis 46 0.022
921
c PLY026 Polycystic Kidney Disease, Autosomal Dominant 46 0.022
922
TLN003 Telangiectasis 46 0.022
923
P ATS008 Autosomal Dominant Disease 46 0.022
924
MTS001 Mutism 46 0.022
925
HYP054 Hypochromic Anemia 45 0.022
926
RNL022 Renal Vascular Disease 45 0.022
927
DVR002 Diverticulitis 45 0.022
928
PLC005 Placental Insufficiency 44 0.022
929
c MLG086 Malignant Hyperthermia Susceptibility 44 0.022
930
NRL007 Neurologic Diseases 44 0.022
931
RPT002 Ruptured Abdominal Aortic Aneurysm 44 0.022
932
CRB036 Cerebral Meningioma 44 0.022
933
BRN014 Bronchopneumonia 44 0.022
934
c MLT074 Multiple Endocrine Neoplasia 43 0.022
935
CNS002 Constrictive Pericarditis 43 0.022
936
c INT060 Intestinal Atresia 43 0.022
937
MNN017 Mononeuropathy 43 0.022
938
LYM011 Lymphogranuloma Venereum 43 0.022
939
TBR008 Tuberculous Peritonitis 43 0.022
940
QDR001 Quadriplegia 43 0.022
941
RFL001 Reflex Sympathetic Dystrophy 43 0.022
942
MYS001 Myositis Ossificans 43 0.022
943
CHR010 Chorioangioma 42 0.022
944
INT052 Intestinal Volvulus 42 0.022
945
RTC005 Reticulosarcoma 42 0.022
946
PNV001 Panuveitis 42 0.022
947
TBR022 Tuberous Sclerosis Complex 41 0.022
948
P BNC001 Bone Carcinoma 41 0.022
949
ORB011 Orbit Rhabdomyosarcoma 41 0.022
950
LYM010 Lymph Node Tuberculosis 41 0.022
951
INP001 Inappropriate Adh Syndrome 41 0.022
952
HYP143 Hypomyelination and Congenital Cataract 41 0.022
953
SPN044 Spinal Cord Ischemia 40 0.022
954
P VGN017 Vaginal Cancer 40 0.022
955
SGN002 Signet Ring Cell Adenocarcinoma 40 0.022
956
INT221 Intravascular Large B-Cell Lymphoma 40 0.022
957
HYP030 Hypoactive Sexual Desire Disorder 39 0.022
958
c FML169 Familial Osteochondritis Dissecans 39 0.022
959
INT071 Intestinal Perforation 39 0.022
960
DGS001 Degos Disease 39 0.022
961
P BRN035 Brain Stem Glioma 38 0.022
962
GST052 Gestational Choriocarcinoma 38 0.022
963
XNT001 Xanthogranulomatous Pyelonephritis 38 0.022
964
ULN001 Ulnar Neuropathy 38 0.022
965
ART012 Aortitis 38 0.022
966
GLY015 Glycine N-Methyltransferase Deficiency 37 0.022
967
P MNN007 Meningocele 37 0.022
968
ACL001 Acalculous Cholecystitis 37 0.022
969
CRB086 Cerebral Aneurysms 37 0.022
970
PLR005 Pleuropneumonia 37 0.022
971
TBR006 Tuberculoid Leprosy 37 0.022
972
SPR007 Superior Mesenteric Artery Syndrome 36 0.022
973
MCK002 Meckel's Diverticulum 36 0.022
974
MYL046 Myelodysplastic Syndrome, Somatic 36 0.022
975
STR079 Sturge-Weber Syndrome, Somatic, Mosaic 36 0.022
976
P HMN004 Hemangioma of Liver 35 0.022
977
LNS001 Lens Subluxation 35 0.022
978
OPT006 Optic Nerve Disease 35 0.022
979
IMG001 Image Syndrome 34 0.022
980
ERY045 Erythrocytosis, Somatic 33 0.022
981
P BNL002 Bone Lymphoma 33 0.022
982
ANG017 Angiolipoma 33 0.022
983
ADS002 Adie Syndrome 33 0.022
984
PRN007 Perinephritis 33 0.022
985
BRD005 Borderline Leprosy 33 0.022
986
SBC014 Subclavian Steal Syndrome 33 0.022
987
ILS001 Ileus 33 0.022
988
SLL001 Sialolithiasis 33 0.022
989
DFC001 Defective Apolipoprotein B-100 32 0.022
990
STR044 Steroid-Resistant Nephrotic Syndrome 31 0.022
991
P CMM008 Communicating Hydrocephalus 31 0.022
992
PNL013 Penile Disease 31 0.022
993
ESN020 Eosinophilic Granulomatosis with Polyangiitis 30 0.022
994
HMP018 Hemophilic Arthropathy 29 0.022
995
DXT002 Dextrocardia with Situs Inversus 29 0.022
996
INT042 Internuclear Ophthalmoplegia 29 0.022
997
c CHR091 Chronic Meningitis 29 0.022
998
SPL012 Splenic Disease 29 0.022
999
c ACQ010 Acquired Polycythemia 29 0.022
1000
ANT013 Anterior Spinal Artery Syndrome 28 0.022
1001
EXN003 Exencephaly 28 0.022
1002
SPL007 Splenic Abscess 28 0.022
1003
MCR216 Microcephaly with or Without Chorioretinopathy, Lymphedema, or Mental Retardation 28 0.022
1004
SLN001 Silent Myocardial Infarction 28 0.022
1005
PLS008 Plasmodium Malariae Malaria 28 0.022
1006
P DCR004 Dacryocystitis 27 0.022
1007
TST020 Testis Seminoma 27 0.022
1008
MDD003 Middle Cerebral Artery Infarction 27 0.022
1009
CGN002 Cogan's Syndrome 27 0.022
1010
RPT003 Ruptured Aortic Aneurysm 27 0.022
1011
HRT006 Heart Aneurysm 26 0.022
1012
CHR034 Chromophobe Adenoma 26 0.022
1013
P SYS007 Systemic Capillary Leak Syndrome 25 0.022
1014
P FML179 Familial Erythrocytosis 2 25 0.022
1015
EMB002 Embryoma 25 0.022
1016
LVR006 Liver Lymphoma 25 0.022
1017
NNF003 Non-Familial Renal Cell Carcinoma 25 0.022
1018
TST007 Testicular Infarct 24 0.022
1019
CPL011 Capillary Malformations, Congenital, 1, Somatic, Mosaic 24 0.022
1020
P CHR097 Chronic Purulent Otitis Media 24 0.022
1021
NRC015 Neurocutaneous Melanocytosis 24 0.022
1022
DYS013 Dysbaric Osteonecrosis 23 0.022
1023
RHM010 Rheumatic Disease of Mitral Valve 23 0.022
1024
ADS008 Aids, Delayed/rapid Progression to 23 0.022
1025
c PST001 Posterior Myocardial Infarction 23 0.022
1026
SLF001 Sulfhemoglobinemia 22 0.022
1027
BCL003 B-Cell Lymphocytic Neoplasm 22 0.022
1028
NTL001 Nut Allergic Reaction 22 0.022
1029
BLD052 Blood Group Incompatibility 22 0.022
1030
SBS002 Substernal Goiter 22 0.022
1031
P 49X002 49,xxxxy Syndrome 22 0.022
1032
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 22 0.022
1033
CRB005 Cerebral Arteritis 21 0.022
1034
CRN213 Craniosynostosis with Radiohumeral Fusions and Other Skeletal and Craniofacial Anomalies 21 0.022
1035
VRT001 Vertebral Artery Occlusion 21 0.022
1036
MSN003 Mesenteric Vascular Occlusion 21 0.022
1037
MYX006 Myxoid Leiomyosarcoma 21 0.022
1038
OPT010 Optic Papillitis 20 0.022
1039
RNL001 Renal Artery Obstruction 20 0.022
1040
PLY004 Polyp of Corpus Uteri 20 0.022
1041
SCT001 Sciatic Neuropathy 19 0.022
1042
QLT001 Qualitative Platelet Defect 19 0.022
1043
SBC002 Subclavian Artery Aneurysm 19 0.022
1044
c DYS149 Dyskeratosis Congenita, Autosomal Recessive 1 18 0.022
1045
URC003 Urachal Adenocarcinoma 18 0.022
1046
HYP015 Hyperlucent Lung 17 0.022
1047
48X002 48,xxxy Syndrome 17 0.022
1048
CLN018 Colon Sarcoma 17 0.022
1049
GST016 Gastric Signet Ring Cell Adenocarcinoma 16 0.022
1050
HMC016 Homocystinuria Due to Cbs Deficiency 16 0.022
1051
CHR076 Choriocarcinoma of the Testis 15 0.022
1052
WND002 Wandering Spleen 15 0.022
1053
c SBC006 Subacute Leukemia 13 0.022
1054
c THR081 Thrombophilia Due to Factor V Leiden 12 0.022
1055
c CRN177 Coronary Heart Disease 7 12 0.022
1056
TRM002 Traumatic Glaucoma 12 0.022
1057
c CRN176 Coronary Heart Disease 9 11 0.022
1058
MCN005 Mucinous Intrahepatic Cholangiocarcinoma 10 0.022
1059
INT055 Intravascular Fasciitis 10 0.022
1060
ACT050 Acute Inferoposterior Infarction 6 0.022
1061
OCL024 Ocular Neuromyotonia 5 0.022