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

1273 hits were found for 'thrombosis'

# ++ Fam MCID Name MIFTS Score
1
PRT018 Portal Vein Thrombosis 54 5.738
2
SGT001 Sagittal Sinus Thrombosis 43 5.666
3
VNS009 Venous Thrombosis 56 5.193
4
INT078 Intracranial Thrombosis 27 5.128
5
CRN017 Coronary Thrombosis 55 5.036
6
LTR002 Lateral Sinus Thrombosis 21 4.512
7
CVR002 Cavernous Sinus Thrombosis 27 4.204
8
CRT004 Carotid Artery Thrombosis 40 4.072
9
HPT002 Hepatic Vein Thrombosis 59 4.027
10
INT076 Intracranial Sinus Thrombosis 13 3.372
11
CRB132 Cerebral Sinovenous Thrombosis 30 3.221
12
VNS011 Venous Thrombosis, Protection Against 4 2.693
13
THR062 Thrombosis, Hyperhomocysteinemic 10 2.656
14
DPV002 Deep Venous Thrombosis, Protection Against 3 2.599
15
DYS078 Dysfibrinogenemia, Alpha Type, Causing Recurrent Thrombosis 3 2.599
16
c PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 3 2.599
17
MND006 Mondor Disease 18 1.868
18
VNS012 Venous Thoracic Outlet Syndrome 18 1.838
19
SCN046 Secondary Short Bowel Syndrome 8 1.838
20
INF133 Inferior Vena Cava Interruption 29 0.303
21
VNS010 Venous Thromboembolism 54 0.257
22
PRT011 Protein C Deficiency 59 0.250
23
P THR015 Thrombophilia 65 0.236
24
END072 Endotheliitis 51 0.231
25
P MYC007 Myocardial Infarction 82 0.230
26
IDP042 Idiopathic Recurrent Stupor 15 0.226
27
HPR003 Heparin-Induced Thrombocytopenia 55 0.225
28
ANT006 Antiphospholipid Syndrome 64 0.223
29
PLM033 Pulmonary Embolism 60 0.223
30
c THR014 Thrombocytopenia 66 0.217
31
PRT014 Protein S Deficiency 67 0.209
32
TYP018 Type 3 Von Willebrand Disease 17 0.201
33
THR079 Thromboembolism 63 0.191
34
PRX023 Paroxysmal Nocturnal Hemoglobinuria, Somatic 24 0.191
35
PRT056 Protein R Deficiency 20 0.187
36
NSY001 N Syndrome 57 0.181
37
HPT023 Hepatocellular Carcinoma 69 0.180
38
PRX003 Paroxysmal Nocturnal Hemoglobinuria 55 0.180
39
HMC004 Homocysteine Plasma Level 31 0.180
40
SPS077 Sepsis 67 0.173
41
PRP034 Purpura Fulminans 46 0.170
42
P HYP075 Hypertension 76 0.167
43
HYP037 Hyperhomocysteinemia 55 0.161
44
c LPS004 Lupus Erythematosus 65 0.159
45
VND001 Vein Disease 42 0.159
46
c ESS003 Essential Thrombocythemia 60 0.157
47
P SYS001 Systemic Lupus Erythematosus 83 0.156
48
c NPH012 Nephrotic Syndrome 57 0.155
49
c XP2001 Xp22.3 Microdeletion Syndrome 17 0.153
50
c ACT075 Acute Myocardial Infarction 59 0.149
51
SYS011 Systemic Lupus Erythematosus, Association with 28 0.148
52
ULC004 Ulcerative Colitis 71 0.145
53
c PRG060 Pregnancy Loss 48 0.142
54
SDD005 Sudden Cardiac Death Multi-Gene Panels 19 0.142
55
THR035 Thrombasthenia 49 0.138
56
LKM002 Leukemia 70 0.137
57
c AFB001 Afibrinogenemia 52 0.137
58
ANK002 Ankylosing Spondylitis 75 0.135
59
IRN001 Iron Deficiency Anemia 58 0.134
60
MTH044 Mthfr Gene Mutation 32 0.132
61
FCT013 Factor V Leiden Thrombophilia 31 0.129
62
PRP030 Purpura 60 0.126
63
INT075 Intracranial Hypertension 53 0.126
64
THR016 Thrombophlebitis 61 0.124
65
PLY018 Polycythemia 55 0.124
66
PLY001 Polycythemia Vera 77 0.122
67
HMG002 Hemoglobinuria 52 0.122
68
LVR012 Liver Cirrhosis 69 0.119
69
THR004 Thrombocytosis 61 0.119
70
FCT006 Factor V Deficiency 58 0.119
71
P CRT049 Critical Limb Ischemia 58 0.119
72
14Q004 14q22q23 Microdeletion Syndrome 25 0.119
73
c HRD066 Hereditary Angioedema Type Iii 23 0.119
74
3Q2005 3q26q27 Microdeletion Syndrome 14 0.119
75
P PRT013 Portal Hypertension 65 0.117
76
c MYL014 Myeloproliferative Disorder 54 0.117
77
P CHR466 Chronic Thromboembolic Pulmonary Hypertension 51 0.117
78
NNT024 Neonatal Stroke 47 0.117
79
CTS005 Catastrophic Antiphospholipid Syndrome 43 0.117
80
PSD002 Pseudotumor Cerebri 43 0.117
81
P SPR035 Superior Vena Cava Syndrome 34 0.117
82
THR013 Thoracic Outlet Syndrome 53 0.116
83
ATH003 Atherosclerosis 69 0.114
84
CRB009 Cerebritis 46 0.114
85
VSC007 Vascular Disease 69 0.112
86
ACT073 Acute Leukemia 62 0.112
87
HDC001 Headache 58 0.112
88
c LCL006 Localized Scleroderma 64 0.110
89
MYC065 Myocardial Infarction, Decreased 33 0.110
90
FTL044 Fetal Cytomegalovirus Syndrome 22 0.110
91
PRC016 Pre-Eclampsia 64 0.108
92
CLL003 Cellulitis 53 0.108
93
BRN026 Branch Retinal Artery Occlusion 39 0.108
94
ATX002 Ataxia Telangiectasia 81 0.107
95
P HMP004 Hemophilia B 66 0.107
96
DSS009 Disseminated Intravascular Coagulation 59 0.107
97
ISC004 Ischemia 57 0.107
98
PRP028 Peripheral Vertigo 30 0.107
99
P SNS014 Sinusitis 54 0.105
100
c MNN013 Meningitis 62 0.103
101
CYT008 Cytomegalovirus Infection 50 0.101
102
MYC020 Mycobacterium Tuberculosis, Susceptibility to Infection by 32 0.101
103
c ACQ012 Acquired Angioedema 31 0.101
104
ADS010 Aids, Slow Progression to 25 0.101
105
STR067 Stroke, Ischemic 69 0.099
106
HMC014 Homocysteinemia 46 0.099
107
c PRN026 Porencephaly 40 0.099
108
CHL079 Children's Interstitial Lung Disease 39 0.099
109
BLD054 Blood Protein Disease 35 0.099
110
INT003 Intracranial Hypotension 28 0.099
111
c PNC044 Pancreatitis 58 0.097
112
P INF037 Inflammatory Bowel Disease 44 0.097
113
CRN211 Coronary Artery Disease, 68 0.094
114
SPT013 Septic Shock 62 0.094
115
OVR029 Ovarian Hyperstimulation Syndrome 61 0.094
116
OTT002 Otitis Media 54 0.094
117
EVN001 Evans' Syndrome 50 0.094
118
NDL013 Nodular Regenerative Hyperplasia 49 0.094
119
HDN002 Head Injury 49 0.094
120
P DYS026 Dysfibrinogenemia 46 0.094
121
P CRN074 Coronary Artery Aneurysm 45 0.094
122
HYP319 Hypereosinophilic Syndrome, Idiopathic, Resistant to Imatinib 27 0.094
123
BLT017 Bilateral Massive Adrenal Hemorrhage 11 0.094
124
RLP001 Relapsing Polychondritis 66 0.092
125
CRN006 Coronary Aneurysm 45 0.092
126
GNR028 Generalized Essential Telangiectasia 16 0.092
127
P HMC002 Homocystinuria 61 0.090
128
PTN001 Patent Foramen Ovale 56 0.090
129
SCN006 Secondary Syphilis 53 0.090
130
P ISC002 Ischemic Optic Neuropathy 52 0.090
131
SCH018 Schizencephaly 47 0.090
132
c ENC008 Encephalocele 47 0.090
133
CRT015 Carotid Artery Occlusion 40 0.090
134
SPP008 Suppurative Otitis Media 37 0.090
135
c SVR056 Severe Hemophilia a 35 0.090
136
CRK001 Cork-Handlers' Disease 28 0.090
137
P HYP098 Hypereosinophilic Syndrome 61 0.088
138
OST028 Osteochondroma 49 0.088
139
LMR001 Lemierre's Syndrome 31 0.088
140
ANG049 Angioedema Induced by Ace Inhibitors 25 0.088
141
21Q001 21q22.11q22.12 Microdeletion Syndrome 13 0.088
142
ACN002 Acanthosis Nigricans 70 0.085
143
c RTN014 Retinal Artery Occlusion 47 0.085
144
c ACQ014 Acquired Hemophilia 45 0.085
145
P THR045 Thrombotic Thrombocytopenic Purpura, Congenital 35 0.085
146
FLM003 Fulminant Viral Hepatitis 30 0.085
147
c ERL004 Early Yaws 29 0.085
148
c HPT021 Hepatitis 65 0.083
149
APP008 Appendicitis 54 0.083
150
MYL001 Myelitis 51 0.083
151
PRN037 Prinzmetal's Variant Angina 24 0.083
152
MTH028 Mthfr Thermolabile Variant 17 0.083
153
TBR010 Tuberculosis 82 0.081
154
BRN024 Bronchitis 71 0.081
155
THR006 Thromboangiitis Obliterans 67 0.081
156
c ACT027 Acute Pancreatitis 60 0.081
157
P MMB002 Membranous Glomerulonephritis 56 0.081
158
INF034 Infective Endocarditis 44 0.081
159
MLK003 Melkersson-Rosenthal Syndrome 43 0.081
160
BRS090 Breast Reconstruction 39 0.081
161
ORB006 Orbital Cellulitis 28 0.081
162
PHL005 Phlebitis 28 0.081
163
HMR001 Hemorrhagic Thrombocythemia 28 0.081
164
NNS006 Non-Suppurative Otitis Media 24 0.081
165
INT206 Intellectual Deficit, X-Linked - Macrocephaly - Macro-Orchidism 11 0.081
166
MYM001 Myoma 56 0.078
167
PPL021 Papilledema 44 0.078
168
RTR011 Retroperitoneal Fibrosis 42 0.078
169
ENT001 Enterocele 39 0.078
170
PNS012 Paine Syndrome 35 0.078
171
TFT003 Tufting Enteropathy 26 0.078
172
CRN019 Coronary Artery Vasospasm 26 0.078
173
14Q001 14q12 Microdeletion Syndrome 23 0.078
174
c 2P1003 2p13.2 Microdeletion Syndrome 11 0.078
175
P HPT001 Hepatitis C 66 0.075
176
ACT119 Acute Promyelocytic Leukemia 64 0.075
177
c HMP007 Hemophilia 64 0.075
178
GLL008 Gilles De La Tourette Syndrome 60 0.075
179
ANR008 Aneurysm Disease 57 0.075
180
LGG001 Legg-Calve-Perthes Disease 56 0.075
181
CRD137 Cardiogenic Shock 56 0.075
182
SND002 Sneddon Syndrome 51 0.075
183
c TWN006 Twin Twin Transfusion Syndrome 51 0.075
184
CRN020 Coronary Restenosis 45 0.075
185
EGG001 Egg Allergy 43 0.075
186
MNN021 Meningococcemia 42 0.075
187
c SPH018 Spherocytosis, Hereditary, Type 5 31 0.075
188
MLR006 Male Reproductive Organ Cancer 21 0.075
189
c DST058 Distal Monosomy 12p 16 0.075
190
MNS013 Monosomy 13q34 14 0.075
191
CNG298 Congenital Pancreatic Cyst 13 0.075
192
ACT019 Acute Myeloid Leukemia 87 0.073
193
P OBS005 Obesity 79 0.073
194
DFC004 Deficiency Anemia 65 0.073
195
P HYD006 Hydrocephalus 60 0.073
196
P ADN016 Adenocarcinoma 60 0.073
197
c BLN003 Blindness 54 0.073
198
MCS003 Mucous Membrane Pemphigoid 51 0.073
199
P PNC102 Pancreatitis, Chronic 41 0.073
200
ZYG002 Zygomycosis 38 0.073
201
SPL006 Splenic Infarction 36 0.073
202
17Q001 17q21.31 Microdeletion Syndrome 29 0.073
203
c CHR226 Chromosome 1q41-Q42 Deletion Syndrome 23 0.073
204
ESN020 Eosinophilic Granulomatosis with Polyangiitis 21 0.073
205
MCR071 Microdeletion 15q11.2 21 0.073
206
CGH002 Cough Headache 11 0.073
207
P HRD011 Hereditary Spherocytosis 59 0.070
208
DWN001 Down Syndrome 58 0.070
209
MYC002 Mycobacterium Avium Complex Disease 56 0.070
210
LYM019 Lymphosarcoma 53 0.070
211
P RTN022 Retinal Vein Occlusion 53 0.070
212
TBR011 Tuberculous Meningitis 51 0.070
213
c ALM001 Al Amyloidosis 49 0.070
214
c ACR001 Aicardi-Goutieres Syndrome 46 0.070
215
APL006 Aplasia Cutis Congenita 41 0.070
216
ATX019 Ataxia with Vitamin E Deficiency 40 0.070
217
VTM002 Vitamin B12 Deficiency 35 0.070
218
HRD083 Hereditary Antithrombin Deficiency 21 0.070
219
GRF006 Grfoma 20 0.070
220
PRT015 Partial Third-Nerve Palsy 19 0.070
221
PLM108 Pulmonary Interstitial Glycogenosis 18 0.070
222
c TTL001 Total Internal Ophthalmoplegia 17 0.070
223
THY020 Thyroid Hyalinizing Trabecular Adenoma 16 0.070
224
EPT015 Epitheliopathy, Acute Posterior Multifocal Placoid Pigment 16 0.070
225
CNG056 Congenital Antithrombin Deficiency 13 0.070
226
CYT018 Cytochrome P450 2d6 Variant 12 0.070
227
c DBT009 Diabetes Mellitus 68 0.067
228
P MYL005 Myelofibrosis 67 0.067
229
P LVR013 Liver Disease 62 0.067
230
ACQ007 Acquired Immunodeficiency Syndrome 62 0.067
231
FCT001 Factor Viii Deficiency 56 0.067
232
THY033 Thyrotoxicosis 55 0.067
233
c ACT134 Acute Liver Failure 55 0.067
234
P HYP083 Hypopituitarism 53 0.067
235
P MLG002 Malignant Peritoneal Mesothelioma 51 0.067
236
LYM026 Lymphoblastic Leukemia 49 0.067
237
P END033 Endocarditis 42 0.067
238
CHY006 Chylous Ascites 40 0.067
239
PST026 Postphlebitic Syndrome 29 0.067
240
c 2Q3005 2q31.1 Microdeletion Syndrome 22 0.067
241
17Q007 17q11 Microdeletion Syndrome 21 0.067
242
12P001 12p12.1 Microdeletion Syndrome 15 0.067
243
MCR033 Macrocephaly-Capillary Malformation 13 0.067
244
CDS001 Cadasil 80 0.064
245
CRH001 Crohn's Disease 78 0.064
246
PRT036 Peritonitis 67 0.064
247
P BLR001 Biliary Atresia 60 0.064
248
P GLM007 Glomerulonephritis 60 0.064
249
CRB039 Cerebrovascular Disease 53 0.064
250
MYL020 Myelomeningocele 51 0.064
251
RNL014 Renal Cell Carcinoma 51 0.064
252
c CNT016 Central Retinal Vein Occlusion 50 0.064
253
INT007 Intermediate Coronary Syndrome 50 0.064
254
JCB001 Jacobsen Syndrome 49 0.064
255
P THR090 Thrombocythemia 1 48 0.064
256
PNM013 Pneumococcal Meningitis 47 0.064
257
PRT012 Prothrombin Deficiency 46 0.064
258
NNT016 Neonatal Hemochromatosis 41 0.064
259
SML026 Small Fiber Neuropathy 39 0.064
260
SPN185 Spinal Cord Infarction 37 0.064
261
ABD004 Abdominal Tuberculosis 35 0.064
262
YNG002 Young Syndrome 34 0.064
263
HNS001 Hansen's Disease 32 0.064
264
HNM001 Hinman's Syndrome 28 0.064
265
CHR158 Charles Bonnet Syndrome 25 0.064
266
CHL109 Childhood Apraxia of Speech 19 0.064
267
DBL009 Double Inferior Vena Cava 16 0.064
268
P STR035 Streptococcal Group a Invasive Disease 15 0.064
269
P BRS047 Breast Cancer 85 0.060
270
THL005 Thalassemia 69 0.060
271
GLN003 Glanzmann's Thrombasthenia 68 0.060
272
P ANG001 Angelman Syndrome 67 0.060
273
SCK003 Sickle Cell Anemia 67 0.060
274
ART019 Aortic Valve Stenosis 64 0.060
275
ART021 Arteriosclerosis 63 0.060
276
GST009 Gastroschisis 58 0.060
277
HLL004 Hellp Syndrome 54 0.060
278
BCT015 Bacteremia 52 0.060
279
CRD001 Cardiac Tamponade 51 0.060
280
ART004 Aortic Atherosclerosis 51 0.060
281
ANG054 Angina Pectoris 48 0.060
282
c ACT076 Acute Myocarditis 47 0.060
283
P MBS002 Moebius Syndrome 45 0.060
284
RCR001 Recurrent Corneal Erosion 43 0.060
285
P CRV039 Cervicitis 41 0.060
286
MNN014 Mononeuritis 40 0.060
287
ETH009 Ethmoid Sinusitis 40 0.060
288
P DYS142 Dyskeratosis Congenita, Autosomal Recessive 4 40 0.060
289
c ATX010 Ataxia Neuropathy Spectrum 33 0.060
290
WRF001 Warfarin Resistance 33 0.060
291
19Q001 19q13.11 Microdeletion Syndrome 21 0.060
292
P ART022 Arthritis 75 0.057
293
KWS002 Kawasaki Disease 69 0.057
294
NRL016 Neural Tube Defects 69 0.057
295
ACT074 Acute Lymphocytic Leukemia 69 0.057
296
P LPR003 Leprosy 67 0.057
297
CLN016 Colon Cancer 66 0.057
298
P ATM003 Autoimmune Thyroiditis 66 0.057
299
VSC011 Vasculitis 65 0.057
300
WST001 West Syndrome 64 0.057
301
FCT007 Factor Vii Deficiency 63 0.057
302
ECL001 Eclampsia 62 0.057
303
ART016 Aortic Aneurysm 62 0.057
304
LNG032 Lung Cancer 61 0.057
305
P CRN157 Coronary Heart Disease 59 0.057
306
FCT004 Factor Xii Deficiency 58 0.057
307
SCK005 Sickle Cell Disease 58 0.057
308
c HPT003 Hepatitis a 57 0.057
309
P INT030 Intracranial Aneurysm 55 0.057
310
c HYP076 Hyperthyroidism 55 0.057
311
LPS007 Lupus Nephritis 55 0.057
312
SRC014 Sarcoma 54 0.057
313
c MLG069 Malignant Hypertension 53 0.057
314
P CNG019 Congenital Afibrinogenemia 52 0.057
315
HYP063 Hypersplenism 52 0.057
316
NTR003 Natural Killer Cell Leukemia 52 0.057
317
P SPH001 Sapho Syndrome 51 0.057
318
c MNT147 Mental Retardation 51 0.057
319
P PND001 Pain Disorder 49 0.057
320
P CNT028 Central Retinal Artery Occlusion 47 0.057
321
ANG011 Angiodysplasia 47 0.057
322
VRC005 Varicose Veins 46 0.057
323
INF013 Inferior Myocardial Infarction 37 0.057
324
P PRV002 Periventricular Nodular Heterotopia 37 0.057
325
SPH007 Sphenoid Sinusitis 33 0.057
326
ACQ017 Acquired Von Willebrand Syndrome 32 0.057
327
P SLP004 Salpingo-Oophoritis 30 0.057
328
MTH027 Mthfr Deficiency 30 0.057
329
CRN185 Craniofacial Deafness Hand Syndrome 28 0.057
330
c CHR266 Chromosome 8p23.1 Deletion 21 0.057
331
CRN220 Craniodiaphyseal Dysplasia, Autosomal Dominant 20 0.057
332
BNT001 Banti's Syndrome 17 0.057
333
c BNG076 Benign Exophthalmos Syndrome 17 0.057
334
c CRN172 Coronary Heart Disease 3 15 0.057
335
SNG003 Single Ventricular Heart 15 0.057
336
c CRN178 Coronary Heart Disease 6 14 0.057
337
APL001 Aplastic Anemia 77 0.053
338
P TRN020 Turner Syndrome 71 0.053
339
DBT001 Diabetic Ketoacidosis 67 0.053
340
MYL006 Myeloid Leukemia 64 0.053
341
ART005 Arteriovenous Malformation 62 0.053
342
VNW001 Von Willebrand's Disease 55 0.053
343
FCT003 Factor X Deficiency 54 0.053
344
INT002 Intermittent Claudication 54 0.053
345
CHL067 Cholecystitis 53 0.053
346
VNS003 Venous Insufficiency 52 0.053
347
ART001 Arterial Tortuosity Syndrome 52 0.053
348
HPT019 Hepatic Encephalopathy 51 0.053
349
PLC007 Placental Abruption 51 0.053
350
HMR003 Hemorrhagic Disease 49 0.053
351
P CHR092 Chronic Myeloproliferative Disease 48 0.053
352
INV001 Invasive Aspergillosis 47 0.053
353
SFT003 Soft Tissue Sarcoma 46 0.053
354
c HPT073 Hepatitis C Virus 43 0.053
355
SVR005 Severe Pre-Eclampsia 43 0.053
356
SCR024 Sacrococcygeal Teratoma 42 0.053
357
ERY004 Erysipelas 41 0.053
358
AND003 Andersen-Tawil Syndrome 39 0.053
359
HYD028 Hydrops, Ectopic Calcification, Moth-Eaten Skeletal Dysplasia 37 0.053
360
FRN014 Fournier Gangrene 36 0.053
361
17Q004 17q12 Microdeletion Syndrome 32 0.053
362
IMM020 Immunodeficiency with Hyper Igm Type 2 29 0.053
363
SBD001 Subdural Empyema 28 0.053
364
PRR008 Periarteritis Nodosa 27 0.053
365
c CRN173 Coronary Heart Disease 8 13 0.053
366
PLM062 Pulmonary Hyalinizing Granuloma 11 0.053
367
P RTT002 Rett Syndrome 75 0.049
368
BRK003 Burkitt's Lymphoma 71 0.049
369
P PRD006 Prader-Willi Syndrome 69 0.049
370
ASP006 Aspergillosis 68 0.049
371
P PNM007 Pneumonia 67 0.049
372
CHR065 Chronic Myeloid Leukemia 67 0.049
373
KLN001 Klinefelter's Syndrome 66 0.049
374
P ABD003 Abdominal Aortic Aneurysm 65 0.049
375
c HYP095 Hypercholesterolemia 65 0.049
376
ATM004 Autoimmune Thrombocytopenic Purpura 62 0.049
377
FCT002 Factor Xi Deficiency 56 0.049
378
CHR001 Churg-Strauss Syndrome 56 0.049
379
c THR005 Thrombotic Thrombocytopenic Purpura 55 0.049
380
ATM010 Autoimmune Hemolytic Anemia 55 0.049
381
P ESN007 Eosinophilia 54 0.049
382
NRP001 Neuropathy 54 0.049
383
HRD057 Hereditary Pancreatitis 53 0.049
384
THY089 Thymic Epithelial Neoplasm 53 0.049
385
CHR074 Choriocarcinoma 52 0.049
386
CCN002 Cocaine Abuse 52 0.049
387
CHL069 Cholesteatoma 52 0.049
388
PRP007 Priapism 52 0.049
389
CRY005 Cryptococcosis 51 0.049
390
ENT015 Enthesitis-Related Arthritis 50 0.049
391
RFR010 Refractory Anemia 50 0.049
392
SPN035 Spindle Cell Sarcoma 50 0.049
393
SYN036 Syncope 49 0.049
394
PRC013 Pericarditis 48 0.049
395
UTR039 Uterine Fibroid 48 0.049
396
WBR001 Weber Syndrome 47 0.049
397
CRN030 Coronary Stenosis 47 0.049
398
CMB021 Combined Pituitary Hormone Deficiency 46 0.049
399
STN007 Stenotrophomonas Maltophilia 46 0.049
400
PRT019 Protein-Losing Enteropathy 46 0.049
401
P CMP008 Compartment Syndrome 45 0.049
402
PYM001 Pyomyositis 44 0.049
403
FCL012 Facial Paralysis 44 0.049
404
PTR001 Petrositis 44 0.049
405
FSC004 Fasciitis 44 0.049
406
FCT005 Factor Xiii Deficiency 44 0.049
407
1P3001 1p36 Deletion Syndrome 44 0.049
408
HPT032 Hepatocellular Carcinoma, Somatic 43 0.049
409
ANT009 Antithrombin Iii Deficiency 43 0.049
410
LYM014 Lymphangitis 42 0.049
411
RTN021 Retinal Vascular Occlusion 42 0.049
412
BWN003 Bowenoid Papulosis 39 0.049
413
OBS004 Obstructive Hydrocephalus 39 0.049
414
VTM001 Vitamin K Deficiency Hemorrhagic Disease 38 0.049
415
ENC017 Encephaloceles 36 0.049
416
NNT020 Neonatal Intrahepatic Cholestasis Caused by Citrin Deficiency 33 0.049
417
ACT099 Acute Fatty Liver of Pregnancy 32 0.049
418
MSM007 Mesomelic Dysplasia Kantaputra Type 32 0.049
419
MYH004 Myh9 Related Thrombocytopenia 31 0.049
420
c FRN011 Frontal Sinusitis 28 0.049
421
JVN024 Juvenile Hereditary Hemochromatosis 28 0.049
422
PTL001 Patulous Eustachian Tube 28 0.049
423
GLM037 Glioma Somatic 27 0.049
424
c HMP017 Hemophilia a, Congenital 26 0.049
425
BSL004 Basilar Artery Occlusion 26 0.049
426
FTL012 Fetal and Neonatal Alloimmune Thrombocytopenia 26 0.049
427
PRT045 Prothrombin-Related Thrombophilia 23 0.049
428
c CRN174 Coronary Heart Disease 2 23 0.049
429
P DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 23 0.049
430
P HYP078 Hypertrophy of Breast 20 0.049
431
AND005 Androgen Insensitivity Syndrome, Mild 19 0.049
432
THN005 Thunderclap Headache 17 0.049
433
HGH021 Hughes-Stovin Syndrome 16 0.049
434
CNG058 Congenital Antithrombin Deficiency Type 3 16 0.049
435
PL2001 Pla2g6-Associated Neurodegeneration 14 0.049
436
12Q001 12q15q21.1 Microdeletion Syndrome 14 0.049
437
AND002 Androgen Insensitivity Syndrome 75 0.045
438
P FML018 Familial Mediterranean Fever 73 0.045
439
PHC003 Pheochromocytoma 71 0.045
440
BTT002 Beta Thalassemia 69 0.045
441
c MST009 Mastocytosis 67 0.045
442
TKY001 Takayasu's Arteritis 65 0.045
443
SPN186 Spinal Cord Injury 63 0.045
444
MRB003 Morbid Obesity 60 0.045
445
TYP007 Typhoid Fever 60 0.045
446
CCT002 Cicatricial Pemphigoid 58 0.045
447
c VRL010 Viral Hepatitis 57 0.045
448
c AXN002 Axenfeld-Rieger Syndrome 57 0.045
449
ADR015 Adrenocortical Carcinoma 57 0.045
450
P BRN019 Bernard-Soulier Syndrome 56 0.045
451
SCR008 Scrub Typhus 55 0.045
452
NPH051 Nephritis 55 0.045
453
P LMY004 Leiomyosarcoma 53 0.045
454
c MYL007 Myeloma 53 0.045
455
ANR004 Anuria 53 0.045
456
OST017 Osteomyelitis 53 0.045
457
ANG018 Angiomyolipoma 52 0.045
458
DND001 Dandy-Walker Syndrome 52 0.045
459
P EXP004 Exophthalmos 51 0.045
460
P PYL005 Pyelonephritis 51 0.045
461
c EPS003 Episodic Ataxia 50 0.045
462
EXS001 Exostosis 49 0.045
463
c ERY013 Erythrocytosis 48 0.045
464
HMR002 Hemarthrosis 48 0.045
465
PLV003 Pelvic Inflammatory Disease 48 0.045
466
CNV002 Conversion Disorder 48 0.045
467
c MTR012 Mitral Valve Disease 48 0.045
468
P LBY004 Labyrinthitis 47 0.045
469
c INT070 Intestinal Obstruction 46 0.045
470
RDC002 Radiculopathy 46 0.045
471
CRT012 Cortical Blindness 44 0.045
472
TRC023 Trichinosis 43 0.045
473
PRR002 Pure Red-Cell Aplasia 42 0.045
474
MYS001 Myositis Ossificans 42 0.045
475
SCT002 Scotoma 41 0.045
476
c CRT018 Carotid Intimal Medial Thickness 39 0.045
477
GNT031 Genitopatellar Syndrome 39 0.045
478
CDQ001 Cauda Equina Syndrome 39 0.045
479
MSS002 Mass Syndrome 37 0.045
480
c 3Q2003 3q29 Microdeletion Syndrome 37 0.045
481
P WRF002 Warfarin Sensitivity 36 0.045
482
AMR003 Amaurosis Fugax 35 0.045
483
HMR039 Hemorrhage, Intracerebral 35 0.045
484
PNG002 Pain Agnosia 34 0.045
485
TYP013 Type 1 Von Willebrand Disease 32 0.045
486
TXC001 Toxic Megacolon 28 0.045
487
12Q002 12q14 Microdeletion Syndrome 28 0.045
488
MLG041 Malignant Triton Tumor 28 0.045
489
INT042 Internuclear Ophthalmoplegia 27 0.045
490
GNT005 Giant Hemangioma 27 0.045
491
2Q3003 2q32q33 Microdeletion Syndrome 25 0.045
492
c 2Q2001 2q23.1 Microdeletion Syndrome 25 0.045
493
c 4Q2001 4q21 Microdeletion Syndrome 24 0.045
494
c OPT031 Optic Neuropathy, Anterior Ischemic 22 0.045
495
SHW001 Shwartzman Phenomenon 22 0.045
496
ADS007 Aids, Rapid Progression to 21 0.045
497
P MLT009 Multiple Cranial Nerve Palsy 20 0.045
498
c KRN003 Kernicterus Due to Isoimmunization 18 0.045
499
P OCL041 Oculomotor Apraxia Cogan Type 17 0.045
500
c THR023 Thrombophilia Due to Thrombomodulin Defect 10 0.045
501
P ALZ001 Alzheimer's Disease 93 0.040
502
P FML021 Familial Hypercholesterolemia 76 0.040
503
P MLT020 Multiple Sclerosis 75 0.040
504
BHC002 Behcet's Disease 68 0.040
505
P WGN002 Wegener's Granulomatosis 67 0.040
506
P MNN012 Meningioma 67 0.040
507
P PLY011 Polycystic Ovary Syndrome 66 0.040
508
IRR002 Irritable Bowel Syndrome 65 0.040
509
P TMP003 Temporal Arteritis 64 0.040
510
P GRV001 Graves' Disease 63 0.040
511
PMS001 Poems Syndrome 61 0.040
512
BRN106 Burns 61 0.040
513
HML002 Hemolytic Anemia 60 0.040
514
HYP066 Hyperglycemia 59 0.040
515
SPT004 Septic Arthritis 59 0.040
516
BCL009 B-Cell Chronic Lymphocytic Leukemia 59 0.040
517
P MLG075 Malignant Mesothelioma 58 0.040
518
SLP006 Sleep Apnea 57 0.040
519
c ATX004 Ataxia 56 0.040
520
P DBT005 Diabetes Insipidus 56 0.040
521
c ENC004 Encephalitis 56 0.040
522
P MLN008 Melanoma 56 0.040
523
c EMR001 Emery-Dreifuss Muscular Dystrophy 56 0.040
524
P LPS002 Liposarcoma 54 0.040
525
c KDN018 Kidney Disease 52 0.040
526
RNL015 Renal Hypertension 52 0.040
527
c HPT007 Hepatitis E 52 0.040
528
CRN036 Craniopharyngioma 52 0.040
529
ALX001 Alexia 51 0.040
530
CHC001 Chickenpox 51 0.040
531
GRY002 Gray Platelet Syndrome 51 0.040
532
END031 Endometrial Stromal Sarcoma 51 0.040
533
P INT068 Intestinal Disease 51 0.040
534
LYM021 Lymphadenitis 50 0.040
535
CHL004 Cholelithiasis 50 0.040
536
ADL002 Adult Syndrome 50 0.040
537
SPL018 Splenomegaly 50 0.040
538
VRC001 Varicocele 49 0.040
539
TXC012 Toxic Epidermal Necrolysis 49 0.040
540
BLD034 Bile Duct Carcinoma 49 0.040
541
c ACT042 Acute Pyelonephritis 49 0.040
542
MDS022 Mediastinitis 49 0.040
543
CRB086 Cerebral Aneurysms 48 0.040
544
MLT113 Multicentric Castleman Disease 48 0.040
545
OPT009 Optic Neuritis 46 0.040
546
CRN029 Coronary Arteriosclerosis 45 0.040
547
NPH017 Nephrosis 45 0.040
548
c BNG032 Benign Mesothelioma 45 0.040
549
CRB004 Cerebral Artery Occlusion 45 0.040
550
IRN002 Iron Metabolism Disease 44 0.040
551
TRP002 Tropical Spastic Paraparesis 44 0.040
552
BNS003 Binswanger's Disease 42 0.040
553
SCT005 Scott Syndrome 42 0.040
554
HPT008 Hepatic Tuberculosis 41 0.040
555
ACT055 Actinomycosis 40 0.040
556
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 40 0.040
557
LPD004 Lipoid Nephrosis 40 0.040
558
PRS045 Prostatic Hypertrophy 38 0.040
559
BNM005 Bone Marrow Necrosis 35 0.040
560
SPR007 Superior Mesenteric Artery Syndrome 35 0.040
561
c CMP058 Complex Regional Pain Syndrome Type 1 35 0.040
562
EMN001 Emanuel Syndrome 34 0.040
563
PRS021 Prostatic Adenoma 34 0.040
564
SCR015 Scarlet Fever 34 0.040
565
MTR001 Mature Cataract 32 0.040
566
MCR029 Micro Syndrome 31 0.040
567
IDP021 Idiopathic Myopathy 29 0.040
568
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 29 0.040
569
c ACT036 Acute Cholangitis 25 0.040
570
LKM059 Leukemia, Megakaryoblastic, with or Without Down Syndrome, Somatic 24 0.040
571
TYP015 Type 2b Von Willebrand Disease 23 0.040
572
RHB020 Rhabdomyosarcoma, Somatic 23 0.040
573
MGL022 Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome, Somatic 23 0.040
574
CHR176 Chromophil Renal Cell Carcinoma 20 0.040
575
NNT025 Neonatal Systemic Lupus Erythematosus 19 0.040
576
HMC030 Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency 14 0.040
577
c CRN175 Coronary Heart Disease 4 14 0.040
578
CMV001 Cmv Antenatal Infection 13 0.040
579
PTT043 Pituitary Hormone Deficiency, Combined, 6 13 0.040
580
ORB016 Orbital Varix 10 0.040
581
CYS001 Cystic Fibrosis 91 0.035
582
P RHM011 Rheumatoid Arthritis 83 0.035
583
P TBR001 Tuberous Sclerosis 81 0.035
584
P MLT019 Multiple Myeloma 76 0.035
585
P PRM021 Primary Pulmonary Hypertension 74 0.035
586
OVR042 Ovarian Cancer 73 0.035
587
MYL040 Myelodysplastic Syndromes 72 0.035
588
PRP027 Peripheral Vascular Disease 71 0.035
589
P CLC005 Celiac Disease 71 0.035
590
P AST007 Astrocytoma 70 0.035
591
ADN018 Adenoma 67 0.035
592
P ADL010 Adult Respiratory Distress Syndrome 66 0.035
593
HYP056 Hypoglycemia 66 0.035
594
AMN001 Amenorrhea 63 0.035
595
P MGR002 Migraine 61 0.035
596
MYS005 Myositis 61 0.035
597
HYD012 Hydrops Fetalis 61 0.035
598
KLP002 Klippel-Trenaunay Syndrome 60 0.035
599
BRN029 Brain Disease 60 0.035
600
DRM006 Dermatitis 60 0.035
601
CRY004 Cryoglobulinemia 59 0.035
602
c HPT015 Hepatitis D 59 0.035
603
SCH014 Schistosomiasis 59 0.035
604
CRB037 Cerebral Palsy 58 0.035
605
CRB021 Cerebral Malaria 58 0.035
606
PHR003 Pharyngitis 57 0.035
607
TNS005 Tonsillitis 57 0.035
608
P CMP010 Complex Regional Pain Syndrome 57 0.035
609
GLB015 Glioblastoma Multiforme 57 0.035
610
BRN071 Brain Injury 57 0.035
611
c MLR021 Malaria, Severe 56 0.035
612
STS002 Situs Inversus 56 0.035
613
ASP003 Aseptic Meningitis 56 0.035
614
CHR090 Chronic Lymphocytic Leukemia 56 0.035
615
BRN004 Brain Edema 55 0.035
616
PPT003 Peptic Ulcer 55 0.035
617
P PNC001 Pancytopenia 55 0.035
618
HYP080 Hypogonadism 54 0.035
619
DDN006 Duodenitis 54 0.035
620
TRM010 Traumatic Brain Injury 54 0.035
621
URM002 Uremia 54 0.035
622
LYM040 Lymphoblastic Lymphoma 54 0.035
623
P BRN009 Burning Mouth Syndrome 54 0.035
624
P MLG077 Malignant Peripheral Nerve Sheath Tumor 53 0.035
625
P MYM002 Moyamoya Disease 52 0.035
626
P CLL015 Collagen Disease 52 0.035
627
HML001 Hemolytic-Uremic Syndrome 52 0.035
628
P PRT039 Proteinuria 51 0.035
629
CLS010 Cluster Headache 51 0.035
630
MGC001 Megacolon 50 0.035
631
HST009 Histiocytoma 49 0.035
632
P LYM025 Lymphedema 49 0.035
633
NPH011 Nephroblastoma 49 0.035
634
ACT115 Acute Myeloid Leukemia, Adult 49 0.035
635
c CTR002 Cataract 48 0.035
636
CLL002 Collecting Duct Carcinoma 48 0.035
637
RHB003 Rhabdomyosarcoma 48 0.035
638
P END047 Endophthalmitis 48 0.035
639
CVR006 Cavernous Hemangioma 47 0.035
640
INF058 Inflammatory Myofibroblastic Tumor 47 0.035
641
P CRB126 Cerebral Cavernous Malformation 47 0.035
642
PRC012 Pericardial Effusion 47 0.035
643
TRN007 Transsexualism 47 0.035
644
CRV031 Cervical Adenocarcinoma 46 0.035
645
c OPH004 Ophthalmoplegia 46 0.035
646
BCK006 Back Pain 46 0.035
647
NRT004 Neuritis 46 0.035
648
CRB088 Cerebral Atrophy 46 0.035
649
TXC002 Toxic Encephalopathy 45 0.035
650
ESN011 Eisenmenger Syndrome 44 0.035
651
ALC005 Alcoholic Pancreatitis 44 0.035
652
CNS002 Constrictive Pericarditis 43 0.035
653
PRP016 Paraplegia 42 0.035
654
LNG029 Lung Adenocarcinoma 42 0.035
655
QDR001 Quadriplegia 42 0.035
656
GST040 Gastric Adenocarcinoma 41 0.035
657
END021 Endomyocardial Fibrosis 40 0.035
658
STR044 Steroid-Resistant Nephrotic Syndrome 40 0.035
659
EPD005 Epidural Abscess 39 0.035
660
PLR007 Pleural Empyema 37 0.035
661
PRL008 Paralytic Ileus 37 0.035
662
STR037 Stress Cardiomyopathy 37 0.035
663
CNT060 Central Serous Chorioretinopathy 35 0.035
664
c SBC003 Subacute Bacterial Endocarditis 35 0.035
665
HNC001 Henoch-Schoenlein Purpura 35 0.035
666
STR080 Stroke, Hemorrhagic 34 0.035
667
MNC006 Monoclonal Gammopathy of Uncertain Significance 34 0.035
668
DYS036 Dysequilibrium Syndrome 32 0.035
669
GRD005 Geroderma Osteodysplasticum 31 0.035
670
PLS018 Plasminogen Activator Inhibitor Type 1 Deficiency 31 0.035
671
DYS003 Dysgraphia 30 0.035
672
15Q001 15q13.3 Microdeletion 29 0.035
673
PTT021 Pituitary Hormone Deficiency, Combined 2 28 0.035
674
c DPH016 Diaphragmatic Hernia 3 27 0.035
675
ART007 Aorta Atresia 26 0.035
676
ORB013 Orbital Disease 25 0.035
677
RHS001 Rh Isoimmunization 24 0.035
678
DFN039 Deafness-Infertility Syndrome 24 0.035
679
c GLM039 Glomerulosclerosis, Focal Segmental, 6 24 0.035
680
16Q001 16q24.3 Microdeletion Syndrome 23 0.035
681
RPT003 Ruptured Aortic Aneurysm 22 0.035
682
P ATM020 Autoimmune Enteropathy 22 0.035
683
HMC020 Homocystinuria, B6-Responsive and Nonresponsive Types 22 0.035
684
CRT045 Creatine Phosphokinase, Elevated Serum 19 0.035
685
SCT001 Sciatic Neuropathy 18 0.035
686
PRF003 Piriformis Syndrome 18 0.035
687
OPT010 Optic Papillitis 18 0.035
688
ABD009 Abducens Palsy 17 0.035
689
PNT023 Pontine Hemorrhage 17 0.035
690
SGM001 Sigmoid Disease 14 0.035
691
P ISC010 Isochromosome Yp 14 0.035
692
MLT129 Multifocal Atrial Tachycardia 14 0.035
693
THR089 Thrombophilia Due to Protein S Deficiency, Autosomal Dominant 13 0.035
694
CVR001 Cavernous Sinus Meningioma 13 0.035
695
c PPL028 Popliteal Pterygium Syndrome Lethal Type 12 0.035
696
PRN017 Perianal Hematoma 10 0.035
697
PRD026 Pre-Descemet Corneal Dystrophy 9 0.035
698
P PNC035 Pancreatic Cancer 82 0.028
699
P FML011 Familial Adenomatous Polyposis 80 0.028
700
P WSK001 Wiskott-Aldrich Syndrome 76 0.028
701
P LFR001 Li-Fraumeni Syndrome 75 0.028
702
FBR012 Fabry Disease 74 0.028
703
GLC006 Galactosemia 74 0.028
704
c TYP008 Type 1 Diabetes Mellitus 71 0.028
705
P MYS003 Myasthenia Gravis 71 0.028
706
OBS002 Obsessive-Compulsive Disorder 71 0.028
707
P RBN001 Rubinstein-Taybi Syndrome 68 0.028
708
P CLR023 Colorectal Cancer 66 0.028
709
P MLR004 Malaria 66 0.028
710
P MDL005 Medulloblastoma 66 0.028
711
MLG056 Malignant Hyperthermia 66 0.028
712
BRN028 Brain Cancer 65 0.028
713
P SYS004 Systemic Mastocytosis 65 0.028
714
c ESS002 Essential Hypertension 64 0.028
715
STT001 Status Epilepticus 64 0.028
716
c PRM002 Primary Hyperoxaluria 63 0.028
717
SPN038 Spina Bifida 63 0.028
718
CCC001 Coccidioidomycosis 63 0.028
719
P RTH001 Rothmund-Thomson Syndrome 63 0.028
720
c HPT016 Hepatitis B 62 0.028
721
ISC006 Ischemic Heart Disease 62 0.028
722
P PLY014 Polycystic Kidney Disease 62 0.028
723
PLY017 Polyarteritis Nodosa 62 0.028
724
P INS005 Insulin Resistance 62 0.028
725
PLM001 Pulmonary Tuberculosis 62 0.028
726
P STM004 Stomach Cancer 62 0.028
727
OLL001 Ollier Disease 62 0.028
728
GLC003 Glucose Intolerance 62 0.028
729
HMN010 Hemangioma 62 0.028
730
DMN001 Diamond-Blackfan Anemia 61 0.028
731
ADL030 Adult-Onset Still's Disease 61 0.028
732
c THY032 Thyroiditis 61 0.028
733
LMY002 Leiomyoma 61 0.028
734
CHL065 Cholangiocarcinoma 61 0.028
735
P END044 Endometriosis 61 0.028
736
HYP266 Hypoxia 60 0.028
737
P NRB001 Neuroblastoma 60 0.028
738
TXC005 Toxic Shock Syndrome 60 0.028
739
LKC001 Leukocyte Adhesion Deficiency 60 0.028
740
P GST044 Gastritis 59 0.028
741
c HYP061 Hypertrophic Cardiomyopathy 59 0.028
742
c HYP086 Hypothyroidism 59 0.028
743
CYS005 Cysticercosis 59 0.028
744
P CST002 Castleman's Disease 58 0.028
745
BLM002 Bulimia Nervosa 58 0.028
746
MLT074 Multiple Endocrine Neoplasia 58 0.028
747
SMT015 Smith Magenis Syndrome 58 0.028
748
MCR088 Microscopic Polyangiitis 58 0.028
749
MLT001 Multiple Chemical Sensitivity 58 0.028
750
DYS007 Dyskeratosis Congenita 58 0.028
751
CRB042 Cerebellar Ataxia 57 0.028
752
INT051 Intussusception 57 0.028
753
DBN001 Dubin-Johnson Syndrome 57 0.028
754
GNG013 Gingivitis 56 0.028
755
KDN017 Kidney Cancer 56 0.028
756
P OLG002 Oligodendroglioma 56 0.028
757
ARG002 Argininosuccinic Aciduria 56 0.028
758
ART031 Aortic Coarctation 56 0.028
759
P ANP001 Anaplastic Large Cell Lymphoma 56 0.028
760
P RNV001 Renovascular Hypertension 56 0.028
761
TTR001 Tetralogy of Fallot 55 0.028
762
P SHR029 Short Syndrome 55 0.028
763
c RBL001 Rubella 55 0.028
764
P CNJ013 Conjunctivitis 55 0.028
765
ANT011 Antisocial Personality Disorder 55 0.028
766
TRN015 Transient Cerebral Ischemia 55 0.028
767
c EHL001 Ehlers-Danlos Syndrome 55 0.028
768
FDL002 Food Allergy 55 0.028
769
PNH001 Panhypopituitarism 54 0.028
770
c MSC005 Muscular Dystrophy 54 0.028
771
HNT002 Hantavirus Pulmonary Syndrome 54 0.028
772
CRV035 Cervical Cancer 54 0.028
773
P ANG015 Angioedema 54 0.028
774
ACT017 Acute Chest Syndrome 53 0.028
775
RTN023 Retinitis 53 0.028
776
ACR008 Acrocallosal Syndrome 53 0.028
777
PYD001 Pyoderma Gangrenosum 53 0.028
778
TYP011 Typhus 53 0.028
779
P SYR001 Syringomyelia 52 0.028
780
c BCT007 Bacterial Meningitis 52 0.028
781
c CNT035 Central Nervous System Disease 52 0.028
782
ATP002 Atopy 52 0.028
783
P CNG015 Congenital Diaphragmatic Hernia 52 0.028
784
PRN011 Pernicious Anemia 52 0.028
785
ALC009 Alcoholic Liver Cirrhosis 52 0.028
786
JPN002 Japanese Encephalitis 51 0.028
787
P ALV004 Alveolar Rhabdomyosarcoma 51 0.028
788
STS003 Sitosterolemia 51 0.028
789
P HMN013 Hemangiopericytoma 51 0.028
790
P ESP024 Esophagitis 51 0.028
791
HMN016 Hemangioendothelioma 51 0.028
792
P MYC008 Myocarditis 51 0.028
793
CNN005 Connective Tissue Disease 51 0.028
794
P PLC011 Pilocytic Astrocytoma 51 0.028
795
NRN004 Neuroendocrine Tumor 51 0.028
796
OBS001 Obstructive Jaundice 50 0.028
797
CYS009 Cystadenoma 50 0.028
798
CRT013 Carotid Stenosis 50 0.028
799
P CHL066 Cholangitis 50 0.028
800
PLM010 Pulmonary Edema 50 0.028
801
ORL011 Oral Cancer 50 0.028
802
CRT016 Carotid Artery Disease 49 0.028
803
DNG001 Dengue Shock Syndrome 49 0.028
804
RTN018 Retinal Disease 49 0.028
805
ACT095 Acute Biphenotypic Leukemia 49 0.028
806
STT004 Steatorrhea 49 0.028
807
P LCT002 Lactose Intolerance 49 0.028
808
c DRR001 Diarrhea 49 0.028
809
URT010 Ureteral Obstruction 48 0.028
810
c HYD002 Hydronephrosis 48 0.028
811
P ATR005 Atrophic Gastritis 48 0.028
812
NTR021 Nutrition Disease 48 0.028
813
NRR001 Neuroretinitis 48 0.028
814
HMP005 Hemiplegia 47 0.028
815
PNN001 Panniculitis 47 0.028
816
SYN006 Synovial Sarcoma 47 0.028
817
ILS001 Ileus 47 0.028
818
P DNT009 Dentin Dysplasia 46 0.028
819
c PSD003 Pseudohypoaldosteronism 46 0.028
820
c RSM001 Rasmussen Encephalitis 46 0.028
821
MTS001 Mutism 45 0.028
822
PRG008 Paragonimiasis 45 0.028
823
P PLY024 Polymicrogyria 45 0.028
824
INT221 Intravascular Large B-Cell Lymphoma 44 0.028
825
HYP265 Hypotonia 43 0.028
826
LMY003 Leiomyomatosis 43 0.028
827
FRM007 Freeman Sheldon Syndrome 43 0.028
828
PYD002 Pyoderma 43 0.028
829
ANP005 Anaplastic Astrocytoma 43 0.028
830
STR077 Streptococcal Toxic-Shock Syndrome 42 0.028
831
SMN007 Seminoma 42 0.028
832
RFL001 Reflex Sympathetic Dystrophy 42 0.028
833
CRT008 Carotid Artery Dissection 41 0.028
834
TRN012 Transient Global Amnesia 40 0.028
835
LYM012 Lymphoplasmacytic Lymphoma 40 0.028
836
INT052 Intestinal Volvulus 40 0.028
837
WTH001 Withdrawal Disorder 40 0.028
838
HMG003 Hemoglobin E Disease 40 0.028
839
CRN014 Cronkhite-Canada Syndrome 40 0.028
840
HYP030 Hypoactive Sexual Desire Disorder 39 0.028
841
PNC033 Pancreas Adenocarcinoma 39 0.028
842
PRT093 Proteus Syndrome, Somatic 39 0.028
843
BNC001 Bone Carcinoma 39 0.028
844
RBF001 Riboflavin Deficiency 38 0.028
845
KDN015 Kidney Angiomyolipoma 38 0.028
846
P HRN001 Horner's Syndrome 38 0.028
847
CRD016 Cardiac Rupture 37 0.028
848
ESP002 Esophageal Varix 37 0.028
849
PNV001 Panuveitis 36 0.028
850
c CRN035 Cranial Nerve Palsy 35 0.028
851
IPX001 Ipex Syndrome 35 0.028
852
P CHR038 Chronic Maxillary Sinusitis 35 0.028
853
VRL011 Viral Infectious Disease 35 0.028
854
MYS004 Myiasis 34 0.028
855
QBC001 Quebec Platelet Disorder 34 0.028
856
INT079 Intrahepatic Cholangiocarcinoma 34 0.028
857
ANG017 Angiolipoma 32 0.028
858
c FML162 Familial Mediterranean Fever, Ad 32 0.028
859
P HMR005 Hemorrhoid 32 0.028
860
CGN002 Cogan's Syndrome 32 0.028
861
CTR003 Citrin Deficiency 32 0.028
862
LYM020 Lymph Node Cancer 32 0.028
863
ADS002 Adie Syndrome 32 0.028
864
LYM005 Lymphocele 31 0.028
865
c SNS011 Sinus Cancer 30 0.028
866
MLK004 Malakoplakia 30 0.028
867
DFC001 Defective Apolipoprotein B-100 30 0.028
868
P CMM008 Communicating Hydrocephalus 27 0.028
869
EHL006 Ehlers–danlos Syndrome 27 0.028
870
CNT059 Central Post-Stroke Pain 26 0.028
871
WND002 Wandering Spleen 26 0.028
872
P MLD013 Mild Hemophilia a 25 0.028
873
ISC001 Ischemic Neuropathy 25 0.028
874
FBR028 Fibrosing Mediastinitis 25 0.028
875
HPT066 Hepatoportal Sclerosis 25 0.028
876
LGP003 Logopenic Progressive Aphasia 22 0.028
877
MNS009 Monosomy 13q14 22 0.028
878
NTL001 Nut Allergic Reaction 21 0.028
879
ALP044 Alpha-1-Antichymotrypsin Deficiency 21 0.028
880
c SVR057 Severe Hemophilia B 21 0.028
881
3Q2002 3q21q26 Syndrome 20 0.028
882
TYP017 Type 2n Von Willebrand Disease 20 0.028
883
MSN003 Mesenteric Vascular Occlusion 20 0.028
884
ALL012 Allergic Angiitis 20 0.028
885
NNF003 Non-Familial Renal Cell Carcinoma 19 0.028
886
P 19P001 19p13.12 Microdeletion Syndrome 19 0.028
887
c ACT035 Acute Frontal Sinusitis 19 0.028
888
RHM007 Rheumatic Congestive Heart Failure 19 0.028
889
INT147 Intrauterine Growth Restriction, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 19 0.028
890
PLS001 Pulsating Exophthalmos 18 0.028
891
TYP016 Type 2m Von Willebrand Disease 18 0.028
892
ANG022 Angel Shaped Phalangoepiphyseal Dysplasia 18 0.028
893
TYP014 Type 2a Von Willebrand Disease 18 0.028
894
SCN042 Secondary Hypereosinophilic Syndrome 16 0.028
895
MNN005 Meningovascular Neurosyphilis 16 0.028
896
ADS005 Aids Dysmorphic Syndrome 16 0.028
897
THR067 Thrombophilia Due to Protein C Deficiency, Autosomal Dominant 15 0.028
898
21Q002 21q22.13q22.2 Microdeletion Syndrome 14 0.028
899
OTP003 Oto-Palatal-Digital Syndrome 13 0.028
900
MLG057 Malignant Cardiac Peripheral Nerve Sheath Neoplasm 12 0.028
901
MLT037 Multifocal Lymphangioendotheliomatosis with Thrombocytopenia 12 0.028
902
ACT187 Activated Pi3k-Delta Syndrome 12 0.028
903
INF001 Infarct of Liver 11 0.028
904
VSC010 Vascular Tissue Disease 11 0.028
905
CYS035 Cystic Adventitial Disease 10 0.028
906
OCL024 Ocular Neuromyotonia 10 0.028
907
THR088 Thrombophilia Due to Protein S Deficiency, Autosomal Recessive 5 0.028
908
HDG007 Hodgkin's Lymphoma 80 0.020
909
P DLT002 Dilated Cardiomyopathy 74 0.020
910
CNG034 Congestive Heart Failure 74 0.020
911
HRD008 Hereditary Hemorrhagic Telangiectasia 74 0.020
912
c NNN003 Noonan Syndrome 73 0.020
913
P HMC003 Hemochromatosis 73 0.020
914
THY028 Thyroid Cancer 73 0.020
915
PTZ001 Peutz-Jeghers Syndrome 73 0.020
916
P TYP020 Type 1 Diabetes 73 0.020
917
AGR001 Age Related Macular Degeneration 71 0.020
918
DCH001 Duchenne Muscular Dystrophy 70 0.020
919
P PRM006 Primary Biliary Cirrhosis 69 0.020
920
P OST005 Osteogenesis Imperfecta 69 0.020
921
P CHR089 Chronic Kidney Failure 68 0.020
922
RNL002 Renal Agenesis 68 0.020
923
LYM007 Lymphangioleiomyomatosis 67 0.020
924
GST023 Gastric Ulcer 67 0.020
925
CRB011 Cerebrotendinous Xanthomatosis 66 0.020
926
P UVT001 Uveitis 66 0.020
927
FBR011 Fibrodysplasia Ossificans Progressiva 66 0.020
928
ACT033 Acute Intermittent Porphyria 66 0.020
929
P CNG026 Congenital Heart Defect 65 0.020
930
P AMY004 Amyloidosis 65 0.020
931
P ART023 Arthropathy 65 0.020
932
BLL006 Bullous Pemphigoid 65 0.020
933
P ATP001 Atopic Dermatitis 64 0.020
934
P ANR007 Anorexia Nervosa 64 0.020
935
P INF038 Influenza 63 0.020
936
P DDN001 Duodenal Ulcer 63 0.020
937
BCK001 Becker Muscular Dystrophy 62 0.020
938
PLY041 Polymyositis 61 0.020
939
c SPN046 Spinal Muscular Atrophy 60 0.020
940
P OST009 Osteochondritis Dissecans 60 0.020
941
MLD001 Melioidosis 60 0.020
942
MXD005 Mixed Connective Tissue Disease 60 0.020
943
c SRC013 Sarcoidosis 60 0.020
944
ACT010 Acth-Secreting Pituitary Adenoma 60 0.020
945
LPR001 Lepromatous Leprosy 59 0.020
946
ACT020 Acute T Cell Leukemia 59 0.020
947
P ALP009 Alopecia Areata 59 0.020
948
P PLM036 Pulmonary Fibrosis 59 0.020
949
ACT009 Acute Monocytic Leukemia 59 0.020
950
FTT001 Fatty Liver Disease 58 0.020
951
CNT009 Central Core Myopathy 58 0.020
952
DNY001 Denys-Drash Syndrome 58 0.020
953
DST005 Diastrophic Dysplasia 58 0.020
954
P BCL006 B-Cell Lymphomas 58 0.020
955
P PRD008 Periodontitis 58 0.020
956
NNH001 Non-Hodgkin Lymphoma 58 0.020
957
c HRD002 Hereditary Angioedema 58 0.020
958
RNL007 Renal Tubular Acidosis 57 0.020
959
MLL005 Miller-Dieker Syndrome 57 0.020
960
P FRG001 Fragile X Syndrome 57 0.020
961
c PRP029 Porphyria 56 0.020
962
PTT006 Pituitary Adenoma 56 0.020
963
CMP002 Campylobacteriosis 56 0.020
964
MYX005 Myxoid Liposarcoma 56 0.020
965
ACT049 Acute Disseminated Encephalomyelitis 56 0.020
966
NTH001 Netherton Syndrome 56 0.020
967
MLB002 Male Breast Cancer 56 0.020
968
ADN011 Adenoid Cystic Carcinoma 56 0.020
969
PLS006 Plasmodium Vivax Malaria 56 0.020
970
CHL014 Cholera 56 0.020
971
ALV005 Alveolar Soft Part Sarcoma 56 0.020
972
P GTR002 Goiter 55 0.020
973
CHL068 Cholestasis 55 0.020
974
c HRM001 Hermansky-Pudlak Syndrome 55 0.020
975
NRN001 Neuroendocrine Carcinoma 55 0.020
976
c CNG042 Congenital Central Hypoventilation Syndrome 55 0.020
977
THR009 Thrombocytopenia-Absent Radius Syndrome 55 0.020
978
P PLY006 Polydactyly 55 0.020
979
c OST026 Osteogenesis Imperfecta Type I 55 0.020
980
ARS001 Aarskog-Scott Syndrome 55 0.020
981
c SYP003 Syphilis 55 0.020
982
ACS001 Acoustic Neuroma 54 0.020
983
SRS001 Serous Cystadenocarcinoma 54 0.020
984
c VNT002 Ventricular Septal Defect 54 0.020
985
FBR003 Fibrous Histiocytoma 54 0.020
986
c THR003 Thoracic Aortic Aneurysm 54 0.020
987
PYR013 Pyruvate Kinase Deficiency 54 0.020
988
GST037 Gastroparesis 54 0.020
989
BBS001 Babesiosis 54 0.020
990
P XNT003 Xanthomatosis 54 0.020
991
MCN001 Mucinous Adenocarcinoma 54 0.020
992
c FML035 Familial Hyperlipidemia 53 0.020
993
SRT004 Serotonin Syndrome 53 0.020
994
BNF002 Bone Fracture 53 0.020
995
c TRT010 Teratoma 53 0.020
996
TBR022 Tuberous Sclerosis Complex 53 0.020
997
SPR004 Supravalvular Aortic Stenosis 53 0.020
998
P OVR049 Ovarian Disease 53 0.020
999
GSG001 Gas Gangrene 53 0.020
1000
SHR001 Short Bowel Syndrome 53 0.020
1001
NPH010 Nephrosclerosis 53 0.020
1002
c SCL016 Scleroderma 53 0.020
1003
GRW007 Growth Hormone Deficiency 52 0.020
1004
BRN080 Brain Ischemia 52 0.020
1005
BRC012 Brucellosis 52 0.020
1006
HRD012 Hereditary Elliptocytosis 52 0.020
1007
CLD007 Cold Agglutinin Disease 52 0.020
1008
PLS011 Plasmacytoma 52 0.020
1009
BLL003 Bell's Palsy 52 0.020
1010
RHM027 Rheumatic Disease 52 0.020
1011
ECH003 Echinococcosis 52 0.020
1012
DNG003 Dengue Disease 52 0.020
1013
CNG048 Congenital Hepatic Fibrosis 52 0.020
1014
LFT009 Left Ventricular Outflow Tract Obstruction 52 0.020
1015
PSR002 Psoriasis 51 0.020
1016
GST027 Gastric Lymphoma 51 0.020
1017
EPT020 Epithelioid Hemangioendothelioma 51 0.020
1018
TCL003 T Cell Deficiency 51 0.020
1019
MNC007 Monocytic Leukemia 51 0.020
1020
ERY008 Erythromelalgia 51 0.020
1021
ART017 Aortic Disease 51 0.020
1022
P MSC003 Muscular Atrophy 51 0.020
1023
ANK001 Ankylosis 51 0.020
1024
P NRV007 Nervous System Disease 51 0.020
1025
SDR002 Siderosis 50 0.020
1026
PRS047 Prostatitis 50 0.020
1027
LPC002 Lip Cancer 50 0.020
1028
MTN003 Motion Sickness 50 0.020
1029
VGN023 Vaginitis 50 0.020
1030
P CHN012 Chondrosarcoma 50 0.020
1031
TCL004 T-Cell Leukemia 50 0.020
1032
AMY053 Amyloidosis, Secondary 50 0.020
1033
CRT002 Cartilage-Hair Hypoplasia 50 0.020
1034
KMR001 Kimura Disease 50 0.020
1035
c DNT011 Dentinogenesis Imperfecta 50 0.020
1036
P CLC001 Calciphylaxis 49 0.020
1037
HPT014 Hepatorenal Syndrome 49 0.020
1038
MNN009 Meningoencephalitis 49 0.020
1039
c PST005 Posterior Uveitis 49 0.020
1040
P PRT029 Parathyroid Adenoma 49 0.020
1041
NRL005 Neurilemmoma 49 0.020
1042
APH002 Aphasia 49 0.020
1043
P GLC007 Glaucoma 49 0.020
1044
PTT004 Pituitary Apoplexy 48 0.020
1045
SCR002 Scurvy 48 0.020
1046
BRK001 Brooke-Spiegler Syndrome 48 0.020
1047
c ACT078 Acute Porphyria 48 0.020
1048
CRN027 Corneal Neovascularization 48 0.020
1049
SPL004 Splenic Marginal Zone Lymphoma 48 0.020
1050
c LFT003 Left Ventricular Noncompaction 48 0.020
1051
MCN007 Meconium Aspiration Syndrome 47 0.020
1052
RTN025 Retinoschisis 47 0.020
1053
NRN002 Neuronitis 47 0.020
1054
LGN002 Legionellosis 47 0.020
1055
PRT070 Peritoneal Carcinoma 47 0.020
1056
SHH001 Sheehan Syndrome 47 0.020
1057
IMP002 Imperforate Anus 47 0.020
1058
IMP005 Impotence 47 0.020
1059
EBS001 Ebstein Anomaly 47 0.020
1060
GST060 Gastric Cancer, Somatic 47 0.020
1061
SPR016 Spermatic Cord Torsion 47 0.020
1062
END020 Endocardial Fibroelastosis 46 0.020
1063
CHN015 Chondrodysplasia 46 0.020
1064
CHL061 Childhood Leukemia 46 0.020
1065
LMB052 Lumbar Disc Herniation 46 0.020
1066
SCN036 Secondary Progressive Multiple Sclerosis 46 0.020
1067
LGN001 Legionnaires' Disease 46 0.020
1068
MYC005 Myocardial Stunning 46 0.020
1069
TLN003 Telangiectasis 46 0.020
1070
DGS001 Degos Disease 46 0.020
1071
P ATS008 Autosomal Dominant Disease 45 0.020
1072
MCL003 Macular Holes 45 0.020
1073
PRT026 Parotitis 45 0.020
1074
PLM052 Pulmonary Arteriovenous Malformation 45 0.020
1075
c PLY026 Polycystic Kidney Disease, Autosomal Dominant 45 0.020
1076
CYS014 Cystadenocarcinoma 45 0.020
1077
NWB001 Newborn Respiratory Distress Syndrome 45 0.020
1078
P GRM009 Germ Cell Tumors 45 0.020
1079
c HYP273 Hypothyroidism, Congenital, Due to Thyroid Dysgenesis or Hypoplasia 45 0.020
1080
HYP054 Hypochromic Anemia 44 0.020
1081
BRN032 Brain Glioma 44 0.020
1082
P OVR046 Ovarian Cyst 44 0.020
1083
c CNT048 Central Hypoventilation Syndrome 44 0.020
1084
RTN001 Retinal Vasculitis 44 0.020
1085
UTR024 Uterine Carcinosarcoma 44 0.020
1086
ADN027 Adenomyosis 44 0.020
1087
FML164 Familial Hdl Deficiency 43 0.020
1088
PLC001 Placenta Accreta 43 0.020
1089
PLC005 Placental Insufficiency 42 0.020
1090
TKT001 Tako-Tsubo Cardiomyopathy 42 0.020
1091
KLT001 Klatskin's Tumor 42 0.020
1092
PST055 Postural Hypotension 42 0.020
1093
NRF003 Neurofibrosarcoma 42 0.020
1094
CHR101 Char Syndrome 42 0.020
1095
c INT060 Intestinal Atresia 42 0.020
1096
BRN014 Bronchopneumonia 42 0.020
1097
BLR015 Blue Rubber Bleb Nevus Syndrome 42 0.020
1098
HMT018 Hematopoietic Stem Cell Transplantation 41 0.020
1099
LYM011 Lymphogranuloma Venereum 41 0.020
1100
c MLG086 Malignant Hyperthermia Susceptibility 41 0.020
1101
WLL004 Wallerian Degeneration 41 0.020
1102
P HYP071 Hypersensitivity Reaction Type Ii Disease 41 0.020
1103
P MGS003 Meigs Syndrome 41 0.020
1104
c RST002 Restrictive Cardiomyopathy 41 0.020
1105
NRL007 Neurologic Diseases 41 0.020
1106
CLN015 Colon Adenocarcinoma 41 0.020
1107
RTC005 Reticulosarcoma 40 0.020
1108
RPT002 Ruptured Abdominal Aortic Aneurysm 40 0.020
1109
P TRN034 Transverse Myelitis 40 0.020
1110
CHR010 Chorioangioma 40 0.020
1111
TBR008 Tuberculous Peritonitis 40 0.020
1112
ACT128 Acute Hepatic Porphyria 40 0.020
1113
SZR006 Seizure Disorder 40 0.020
1114
HRS011 Horseshoe Kidney 39 0.020
1115
DVR002 Diverticulitis 39 0.020
1116
CNG219 Congenital Aural Atresia 39 0.020
1117
LYM010 Lymph Node Tuberculosis 39 0.020
1118
P TWN001 Twin-to-Twin Transfusion Syndrome 39 0.020
1119
EXN003 Exencephaly 38 0.020
1120
ORB011 Orbit Rhabdomyosarcoma 38 0.020
1121
CTN017 Cutaneous Necrotizing Vasculitis 38 0.020
1122
SGN002 Signet Ring Cell Adenocarcinoma 38 0.020
1123
PLM074 Pulmonary Function 38 0.020
1124
SPN044 Spinal Cord Ischemia 38 0.020
1125
P MNN007 Meningocele 38 0.020
1126
CRB036 Cerebral Meningioma 38 0.020
1127
AMY038 Amyloidosis, Renal 37 0.020
1128
ACL001 Acalculous Cholecystitis 37 0.020
1129
c ACT150 Acute Adrenal Insufficiency 37 0.020
1130
RCT009 Rectosigmoid Cancer 37 0.020
1131
XNT001 Xanthogranulomatous Pyelonephritis 37 0.020
1132
c CRB059 Cerebellar Degeneration 36 0.020
1133
PLR005 Pleuropneumonia 36 0.020
1134
ART012 Aortitis 36 0.020
1135
c FML169 Familial Osteochondritis Dissecans 36 0.020
1136
VGN017 Vaginal Cancer 36 0.020
1137
ULN001 Ulnar Neuropathy 35 0.020
1138
RNL022 Renal Vascular Disease 35 0.020
1139
c RCR022 Recurrent Acute Pancreatitis 35 0.020
1140
MNN017 Mononeuropathy 35 0.020
1141
TBR006 Tuberculoid Leprosy 34 0.020
1142
TST021 Testicular Germ Cell Tumor 34 0.020
1143
P 2Q3002 2q37 Microdeletion Syndrome 34 0.020
1144
c HYP011 Hyperlipoproteinemia Type Iii 34 0.020
1145
INP001 Inappropriate Adh Syndrome 34 0.020
1146
P BRN035 Brain Stem Glioma 34 0.020
1147
LCK001 Locked-in Syndrome 33 0.020
1148
BRN055 Bronchogenic Cyst 33 0.020
1149
HMP018 Hemophilic Arthropathy 33 0.020
1150
SBC014 Subclavian Steal Syndrome 33 0.020
1151
CNG069 Congenital Cytomegalovirus 33 0.020
1152
PRM008 Parametritis 33 0.020
1153
SPR066 Superficial Siderosis 33 0.020
1154
LNS001 Lens Subluxation 32 0.020
1155
P SYS007 Systemic Capillary Leak Syndrome 32 0.020
1156
GLY015 Glycine N-Methyltransferase Deficiency 32 0.020
1157
PRT086 Partial Hydatidiform Mole 32 0.020
1158
BRD005 Borderline Leprosy 32 0.020
1159
MYL046 Myelodysplastic Syndrome, Somatic 32 0.020
1160
INT071 Intestinal Perforation 32 0.020
1161
P OTT001 Otitis Externa 31 0.020
1162
IMR001 Imerslund-Grasbeck Syndrome 31 0.020
1163
P BNL002 Bone Lymphoma 31 0.020
1164
PRN007 Perinephritis 30 0.020
1165
SLL001 Sialolithiasis 30 0.020
1166
FTD001 Foot Drop 30 0.020
1167
HYP143 Hypomyelination and Congenital Cataract 29 0.020
1168
STR026 Star Syndrome 29 0.020
1169
OPT006 Optic Nerve Disease 29 0.020
1170
ANT013 Anterior Spinal Artery Syndrome 28 0.020
1171
HMG001 Hemoglobin C Disease 28 0.020
1172
MDL006 Madelung Disease 28 0.020
1173
STR079 Sturge-Weber Syndrome, Somatic, Mosaic 28 0.020
1174
SPL007 Splenic Abscess 27 0.020
1175
TST020 Testis Seminoma 27 0.020
1176
DFN222 Deafness-Dystonia-Optic Neuronopathy Syndrome 27 0.020
1177
NRS005 Neurosarcoidosis 27 0.020
1178
P PRX010 Paroxysmal Ventricular Fibrillation 26 0.020
1179
SPL012 Splenic Disease 26 0.020
1180
SLS001 Sle Susceptibility 26 0.020
1181
SLN001 Silent Myocardial Infarction 26 0.020
1182
ERY045 Erythrocytosis, Somatic 26 0.020
1183
URC003 Urachal Adenocarcinoma 26 0.020
1184
SGM004 Sigmoid Colon Cancer 26 0.020
1185
FLC001 Folic Acid Deficiency Anemia 26 0.020
1186
ACQ010 Acquired Polycythemia 25 0.020
1187
c 2P2001 2p21 Microdeletion Syndrome 25 0.020
1188
EMB002 Embryoma 25 0.020
1189
P DCR004 Dacryocystitis 24 0.020
1190
HMG004 Hemoglobin D Disease 24 0.020
1191
HRT006 Heart Aneurysm 24 0.020
1192
HYP074 Hypersensitivity Vasculitis 24 0.020
1193
PNL013 Penile Disease 24 0.020
1194
P ANG041 Angioedema, Hereditary, Types I and Ii 24 0.020
1195
P DXT002 Dextrocardia with Situs Inversus 24 0.020
1196
CHR034 Chromophobe Adenoma 24 0.020
1197
TST007 Testicular Infarct 24 0.020
1198
NRC015 Neurocutaneous Melanocytosis 23 0.020
1199
c CHR091 Chronic Meningitis 23 0.020
1200
P CHR097 Chronic Purulent Otitis Media 23 0.020
1201
LPD027 Lip Disease 23 0.020
1202
CLD014 Cole Disease 23 0.020
1203
PLC008 Placenta Disease 22 0.020
1204
DYS013 Dysbaric Osteonecrosis 22 0.020
1205
P CHR259 Chromosome 6q25 Microdeletion Syndrome 22 0.020
1206
CRT028 Cor Triatriatum 22 0.020
1207
ADS008 Aids, Delayed/rapid Progression to 22 0.020
1208
c MYC058 Myocardial Infarction 2 21 0.020
1209
c PST001 Posterior Myocardial Infarction 21 0.020
1210
HMG017 Hemoglobin So 21 0.020
1211
MYX006 Myxoid Leiomyosarcoma 21 0.020
1212
LVR006 Liver Lymphoma 21 0.020
1213
SBS002