Search results for "thrombosis"

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

1541 hits were found for 'thrombosis'

# Family MCID Name MIFTS Score
1
SGT001 Sagittal Sinus Thrombosis 32 5.349
2
CRN017 Coronary Thrombosis 42 5.348
3
INT078 Intracranial Thrombosis 29 5.321
4
PRT018 Portal Vein Thrombosis 41 5.008
5
LTR002 Lateral Sinus Thrombosis 30 4.921
6
CVR002 Cavernous Sinus Thrombosis 28 4.642
7
c THR092 Thrombophilia Due to Thrombin Defect 49 4.604
8
CRT004 Carotid Artery Thrombosis 32 4.052
9
HPT002 Hepatic Vein Thrombosis 32 3.548
10
INT076 Intracranial Sinus Thrombosis 20 3.305
11
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 7 2.652
12
CRB132 Cerebral Sinovenous Thrombosis 30 2.166
13
P BDD001 Budd-Chiari Syndrome 56 2.113
14
FCT013 Factor V Leiden Thrombophilia 43 2.054
15
MND006 Mondor Disease 21 1.927
16
THR055 Thrombophilia, X-Linked, Due to Factor Ix Defect 17 1.887
17
HMC020 Homocystinuria, B6-Responsive and Nonresponsive Types 32 1.875
18
VNS012 Venous Thoracic Outlet Syndrome 17 1.860
19
CRB009 Cerebritis 37 0.429
20
PLM033 Pulmonary Embolism 53 0.255
21
VND001 Vein Disease 34 0.249
22
P MYC007 Myocardial Infarction 76 0.232
23
P HPT021 Hepatitis 58 0.225
24
P THR015 Thrombophilia 52 0.225
25
PRT014 Protein S Deficiency 46 0.221
26
P THR014 Thrombocytopenia 50 0.209
27
HPR003 Heparin-Induced Thrombocytopenia 39 0.201
28
PRT011 Protein C Deficiency 46 0.193
29
P ANT006 Antiphospholipid Syndrome 55 0.189
30
HPT023 Hepatocellular Carcinoma 90 0.176
31
ANR040 Aneurysm 43 0.169
32
GRN039 Greenberg Skeletal Dysplasia 43 0.154
33
c SYS001 Systemic Lupus Erythematosus 90 0.150
34
P LPS004 Lupus Erythematosus 61 0.148
35
END072 Endotheliitis 39 0.147
36
HYP037 Hyperhomocysteinemia 40 0.145
37
P ESS003 Essential Thrombocythemia 63 0.143
38
c ACT075 Acute Myocardial Infarction 50 0.134
39
P NPH012 Nephrotic Syndrome 52 0.133
40
LVR012 Liver Cirrhosis 59 0.129
41
P LKM002 Leukemia 61 0.124
42
PST095 Post-Thrombotic Syndrome 38 0.124
43
ART111 Artery Disease 48 0.121
44
VSC007 Vascular Disease 55 0.120
45
P PLY018 Polycythemia 53 0.120
46
P PNC044 Pancreatitis 51 0.117
47
CLT003 Colitis 47 0.115
48
ATH003 Atherosclerosis 50 0.114
49
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 48 0.112
50
THR016 Thrombophlebitis 48 0.112
51
P PRT013 Portal Hypertension 45 0.112
52
HMG002 Hemoglobinuria 39 0.112
53
PRP027 Peripheral Vascular Disease 62 0.111
54
THR004 Thrombocytosis 48 0.111
55
ULC004 Ulcerative Colitis 75 0.109
56
HDC001 Headache 42 0.109
57
P LVR013 Liver Disease 59 0.106
58
P SNS014 Sinusitis 49 0.105
59
VSC006 Vascular Cancer 40 0.105
60
P CRN211 Coronary Artery Disease 68 0.103
61
P BLD051 Blood Coagulation Disease 30 0.100
62
P MNN013 Meningitis 51 0.098
63
ISC004 Ischemia 47 0.098
64
MST019 Mastoiditis 29 0.098
65
STR067 Stroke, Ischemic 68 0.097
66
BLD053 Blood Platelet Disease 32 0.097
67
RTN023 Retinitis 43 0.095
68
HPT020 Hepatic Vascular Disease 33 0.093
69
GLC006 Galactosemia 76 0.091
70
OTT002 Otitis Media 57 0.091
71
DSS009 Disseminated Intravascular Coagulation 48 0.089
72
PRP030 Purpura 47 0.089
73
INT075 Intracranial Hypertension 46 0.089
74
INT003 Intracranial Hypotension 26 0.089
75
P ADN016 Adenocarcinoma 56 0.088
76
HDN002 Head Injury 38 0.088
77
P ART084 Arteriovenous Fistula 34 0.088
78
P CNG401 Congenital Heart Disease 68 0.086
79
P HYP098 Hypereosinophilic Syndrome 49 0.086
80
P HMC002 Homocystinuria 46 0.086
81
CLL003 Cellulitis 41 0.086
82
OVR029 Ovarian Hyperstimulation Syndrome 57 0.084
83
P VNS003 Venous Insufficiency 44 0.084
84
THR013 Thoracic Outlet Syndrome 47 0.082
85
PSD002 Pseudotumor Cerebri 42 0.082
86
VSC008 Vascular Hemostatic Disease 22 0.082
87
P DYS026 Dysfibrinogenemia 45 0.077
88
ANG054 Angina Pectoris 41 0.077
89
TBR010 Tuberculosis 64 0.075
90
ART021 Arteriosclerosis 51 0.075
91
c MYC058 Myocardial Infarction 2 19 0.075
92
ADJ001 Adjustment Disorder 30 0.073
93
CRN006 Coronary Aneurysm 27 0.071
94
P CRN214 Coronary Heart Disease 5 10 0.071
95
P PLM037 Pulmonary Hypertension 78 0.068
96
P MYL005 Myelofibrosis 64 0.068
97
ISC006 Ischemic Heart Disease 56 0.068
98
DFC004 Deficiency Anemia 52 0.068
99
PTN001 Patent Foramen Ovale 48 0.068
100
c CRN178 Coronary Heart Disease 6 10 0.068
101
CRH001 Crohn's Disease 80 0.066
102
c HYP595 Hypertension, Essential 68 0.066
103
P LYM026 Lymphoblastic Leukemia 57 0.066
104
THR104 Thrombophilia Due to Antithrombin Iii Deficiency 53 0.066
105
P HMP007 Hemophilia 51 0.066
106
MYM001 Myoma 49 0.066
107
FCT004 Factor Xii Deficiency 48 0.066
108
c ACT027 Acute Pancreatitis 47 0.066
109
P ENC018 Encephalopathy 42 0.066
110
CRD137 Cardiogenic Shock 39 0.066
111
PPL021 Papilledema 38 0.066
112
SPL006 Splenic Infarction 35 0.066
113
c CRN175 Coronary Heart Disease 4 9 0.066
114
P OBS005 Obesity 89 0.063
115
c HMP029 Hemophilia a 64 0.063
116
BHC002 Behcet's Disease 63 0.063
117
CRB039 Cerebrovascular Disease 58 0.063
118
HMT002 Hematologic Cancer 53 0.063
119
c ART101 Aortic Valve Disease 2 46 0.063
120
CSY001 C Syndrome 44 0.063
121
LMR001 Lemierre's Syndrome 43 0.063
122
P TRC086 Trichohepatoenteric Syndrome 1 42 0.063
123
ORB006 Orbital Cellulitis 28 0.063
124
P RNL014 Renal Cell Carcinoma 81 0.061
125
P APL001 Aplastic Anemia 70 0.061
126
PRT036 Peritonitis 58 0.061
127
P ATR011 Atrial Fibrillation 55 0.061
128
VSC011 Vasculitis 50 0.061
129
CYT008 Cytomegalovirus Infection 47 0.061
130
IRN001 Iron Deficiency Anemia 47 0.061
131
P OST028 Osteochondroma 40 0.061
132
P SPS003 Spastic Diplegia 37 0.061
133
VSC047 Vascular Malformation 35 0.061
134
SPR035 Superior Vena Cava Syndrome 27 0.061
135
ANR002 Aniridia 72 0.058
136
ART005 Arteriovenous Malformation 56 0.058
137
ACN002 Acanthosis Nigricans 53 0.058
138
P SCK005 Sickle Cell Disease 49 0.058
139
P GLM007 Glomerulonephritis 49 0.058
140
P INT030 Intracranial Aneurysm 41 0.058
141
HRT012 Heart Valve Disease 40 0.058
142
MMB002 Membranous Glomerulonephritis 40 0.058
143
P CRN074 Coronary Artery Aneurysm 37 0.058
144
CRT015 Carotid Artery Occlusion 35 0.058
145
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 34 0.058
146
P ATX010 Ataxia Neuropathy Spectrum 31 0.058
147
P BRS047 Breast Cancer 100 0.055
148
P DBT085 Diabetes Mellitus, Insulin-Dependent 82 0.055
149
SCK003 Sickle Cell Anemia 71 0.055
150
c SPN225 Spondyloarthropathy 1 66 0.055
151
P ANG001 Angelman Syndrome 66 0.055
152
PLY125 Polycythemia Vera, Somatic 62 0.055
153
THR006 Thromboangiitis Obliterans 60 0.055
154
P KDN018 Kidney Disease 57 0.055
155
ART016 Aortic Aneurysm 55 0.055
156
P HYD006 Hydrocephalus 54 0.055
157
P CRD011 Cardiomyopathy 53 0.055
158
P HYP083 Hypopituitarism 45 0.055
159
P END033 Endocarditis 43 0.055
160
P CRV039 Cervicitis 42 0.055
161
P AFB001 Afibrinogenemia 41 0.055
162
HYP063 Hypersplenism 40 0.055
163
THR035 Thrombasthenia 36 0.055
164
c CRN174 Coronary Heart Disease 2 9 0.055
165
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 84 0.052
166
CDS001 Cadasil 70 0.052
167
FCT007 Factor Vii Deficiency 66 0.052
168
VNW001 Von Willebrand's Disease 63 0.052
169
KWS002 Kawasaki Disease 62 0.052
170
P ART022 Arthritis 61 0.052
171
ART001 Arterial Tortuosity Syndrome 59 0.052
172
SRC014 Sarcoma 57 0.052
173
P THL005 Thalassemia 56 0.052
174
c MTB001 Metabolic Syndrome X 52 0.052
175
CHL071 Child Syndrome 51 0.052
176
HPT019 Hepatic Encephalopathy 50 0.052
177
P SHR029 Short Syndrome 49 0.052
178
P ESN007 Eosinophilia 48 0.052
179
HMR001 Hemorrhagic Thrombocythemia 48 0.052
180
BNM001 Bone Marrow Cancer 47 0.052
181
P RTN022 Retinal Vein Occlusion 45 0.052
182
KDS001 Kid Syndrome 44 0.052
183
PRP080 Peripheral Artery Disease 39 0.052
184
SPL012 Splenic Disease 37 0.052
185
c CHR431 Chronic Venous Insufficiency 35 0.052
186
CHR466 Chronic Thromboembolic Pulmonary Hypertension 35 0.052
187
CTS005 Catastrophic Antiphospholipid Syndrome 34 0.052
188
CHY006 Chylous Ascites 33 0.052
189
CRB085 Cerebral Hemorrhage 31 0.052
190
INF001 Infarct of Liver 27 0.052
191
HRD083 Hereditary Antithrombin Deficiency 25 0.052
192
SPH007 Sphenoid Sinusitis 24 0.052
193
INT010 Intracranial Embolism 23 0.052
194
MYT019 May-Thurner Syndrome 18 0.052
195
P ATX030 Ataxia-Telangiectasia 76 0.048
196
P PHC003 Pheochromocytoma 76 0.048
197
MYL009 Myelodysplastic Syndrome 69 0.048
198
c HMP004 Hemophilia B 65 0.048
199
GLN010 Glanzmann Thrombasthenia 65 0.048
200
P MYL006 Myeloid Leukemia 59 0.048
201
P AND016 Andersen Syndrome 58 0.048
202
P PNM007 Pneumonia 56 0.048
203
IMG001 Image Syndrome 56 0.048
204
P HRD011 Hereditary Spherocytosis 52 0.048
205
CHL067 Cholecystitis 51 0.048
206
c THR082 Thrombophilia Due to Activated Protein C Resistance 50 0.048
207
P ABD003 Abdominal Aortic Aneurysm 50 0.048
208
P HYP076 Hyperthyroidism 48 0.048
209
P THR005 Thrombotic Thrombocytopenic Purpura 48 0.048
210
P NRP001 Neuropathy 48 0.048
211
TTH006 Tooth Disease 47 0.048
212
EVN001 Evans' Syndrome 46 0.048
213
SPN020 Spondylosis 46 0.048
214
BRN106 Burns 43 0.048
215
ADL002 Adult Syndrome 43 0.048
216
ART017 Aortic Disease 42 0.048
217
SPP008 Suppurative Otitis Media 41 0.048
218
BCT015 Bacteremia 40 0.048
219
c CHR092 Chronic Myeloproliferative Disease 39 0.048
220
ACT017 Acute Chest Syndrome 39 0.048
221
HRT007 Heart Cancer 34 0.048
222
HMC014 Homocysteinemia 32 0.048
223
P HRT017 Heart Tumor 21 0.048
224
PLM027 Pulmonary Embolism and Infarction 17 0.048
225
c THR023 Thrombophilia Due to Thrombomodulin Defect 16 0.048
226
c ADL079 Adult Heart Tumor 7 0.048
227
c HPT001 Hepatitis C 64 0.045
228
P PRM002 Primary Hyperoxaluria 64 0.045
229
c HPT016 Hepatitis B 59 0.045
230
TKY001 Takayasu's Arteritis 57 0.045
231
P ASP006 Aspergillosis 56 0.045
232
FCT006 Factor V Deficiency 54 0.045
233
P ESP024 Esophagitis 51 0.045
234
c ACT073 Acute Leukemia 49 0.045
235
c INF071 Inflammatory Bowel Disease 1 48 0.045
236
SPH001 Sapho Syndrome 46 0.045
237
BLR001 Biliary Atresia 44 0.045
238
MTH009 Mouth Disease 44 0.045
239
CHL069 Cholesteatoma 43 0.045
240
PRP007 Priapism 41 0.045
241
PRP016 Paraplegia 41 0.045
242
CRD001 Cardiac Tamponade 39 0.045
243
CRP017 Carpal Tunnel Syndrome, Familial 39 0.045
244
RTR011 Retroperitoneal Fibrosis 38 0.045
245
ERY004 Erysipelas 35 0.045
246
MDS022 Mediastinitis 33 0.045
247
GLC008 Glucose Metabolism Disease 30 0.045
248
SPN185 Spinal Cord Infarction 29 0.045
249
PTR001 Petrositis 25 0.045
250
HGH021 Hughes-Stovin Syndrome 21 0.045
251
THR088 Thrombophilia Due to Protein S Deficiency, Autosomal Recessive 17 0.045
252
EYC003 Eye Accommodation Disease 14 0.045
253
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 11 0.045
254
c CRN177 Coronary Heart Disease 7 10 0.045
255
P LNG032 Lung Cancer 91 0.041
256
c MLT019 Multiple Myeloma 77 0.041
257
BRK010 Burkitt Lymphoma 68 0.041
258
AND015 Androgen Insensitivity 65 0.041
259
CNG034 Congestive Heart Failure 65 0.041
260
P LPR003 Leprosy 63 0.041
261
PCK002 Pick Disease 61 0.041
262
P AXN010 Axenfeld-Rieger Syndrome, Type 3 60 0.041
263
P TRN020 Turner Syndrome 59 0.041
264
KLN001 Klinefelter's Syndrome 57 0.041
265
SPN186 Spinal Cord Injury 55 0.041
266
SCH014 Schistosomiasis 55 0.041
267
RBR001 Roberts Syndrome 54 0.041
268
P MYL007 Myeloma 54 0.041
269
P ACR001 Aicardi-Goutieres Syndrome 53 0.041
270
MLK003 Melkersson-Rosenthal Syndrome 53 0.041
271
CHR001 Churg-Strauss Syndrome 53 0.041
272
RLP001 Relapsing Polychondritis 52 0.041
273
DBT001 Diabetic Ketoacidosis 50 0.041
274
VHW001 Vohwinkel Syndrome 50 0.041
275
PRS047 Prostatitis 50 0.041
276
PRN023 Prion Disease 50 0.041
277
OST017 Osteomyelitis 48 0.041
278
LRN003 Learning Disability 47 0.041
279
EXF001 Exfoliation Syndrome 45 0.041
280
NWC001 Newcastle Disease 45 0.041
281
INT007 Intermediate Coronary Syndrome 45 0.041
282
CRD119 Cardiac Arrest 45 0.041
283
P MMB011 Membranous Nephropathy 43 0.041
284
c PND001 Pain Disorder 43 0.041
285
ORL011 Oral Cancer 43 0.041
286
ANR004 Anuria 43 0.041
287
P PYL005 Pyelonephritis 42 0.041
288
BRN071 Brain Injury 42 0.041
289
HLL004 Hellp Syndrome 42 0.041
290
OCL006 Ocular Hypertension 41 0.041
291
CDQ001 Cauda Equina Syndrome 40 0.041
292
CRN030 Coronary Stenosis 40 0.041
293
c CNT016 Central Retinal Vein Occlusion 40 0.041
294
PRT019 Protein-Losing Enteropathy 40 0.041
295
DDN006 Duodenitis 40 0.041
296
EXS001 Exostosis 39 0.041
297
ISC002 Ischemic Optic Neuropathy 38 0.041
298
P RTN014 Retinal Artery Occlusion 38 0.041
299
LPD004 Lipoid Nephrosis 38 0.041
300
LCK001 Locked-in Syndrome 37 0.041
301
SHW001 Shwartzman Phenomenon 36 0.041
302
OBS004 Obstructive Hydrocephalus 35 0.041
303
ZYG002 Zygomycosis 35 0.041
304
CRB004 Cerebral Artery Occlusion 33 0.041
305
ABD004 Abdominal Tuberculosis 33 0.041
306
MDY003 Mody, Type Ii 32 0.041
307
CRB086 Cerebral Aneurysms 32 0.041
308
SBD001 Subdural Empyema 31 0.041
309
NNT024 Neonatal Stroke 31 0.041
310
UND005 Undifferentiated Pleomorphic Sarcoma 31 0.041
311
SXL003 Sexual Disorder 30 0.041
312
VTM001 Vitamin K Deficiency Hemorrhagic Disease 29 0.041
313
c FRN011 Frontal Sinusitis 27 0.041
314
BLD054 Blood Protein Disease 24 0.041
315
ALR002 Al-Raqad Syndrome 23 0.041
316
c THR048 Thrombocytopenia 4 20 0.041
317
THN005 Thunderclap Headache 16 0.041
318
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 15 0.041
319
ORB016 Orbital Varix 12 0.041
320
c CRN176 Coronary Heart Disease 9 9 0.041
321
CGL001 Coagulation Protein Disease 5 0.041
322
TTR001 Tetralogy of Fallot 68 0.036
323
TYP007 Typhoid Fever 59 0.036
324
ABT001 Abetalipoproteinemia 57 0.036
325
ACQ007 Acquired Immunodeficiency Syndrome 55 0.036
326
P TMP003 Temporal Arteritis 53 0.036
327
PRT093 Proteus Syndrome, Somatic 52 0.036
328
P HML002 Hemolytic Anemia 52 0.036
329
APP008 Appendicitis 52 0.036
330
c PRC016 Pre-Eclampsia 51 0.036
331
HYP066 Hyperglycemia 50 0.036
332
ADR015 Adrenocortical Carcinoma 48 0.036
333
P ACT074 Acute Lymphocytic Leukemia 48 0.036
334
BRN004 Brain Edema 47 0.036
335
LYM019 Lymphosarcoma 47 0.036
336
P LMY004 Leiomyosarcoma 47 0.036
337
P ECL001 Eclampsia 47 0.036
338
SND002 Sneddon Syndrome 47 0.036
339
P SLP006 Sleep Apnea 46 0.036
340
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 46 0.036
341
P MTR012 Mitral Valve Disease 46 0.036
342
LPD008 Lipid Metabolism Disorder 45 0.036
343
P INT070 Intestinal Obstruction 45 0.036
344
P THR012 Thoracic Cancer 44 0.036
345
VGN023 Vaginitis 44 0.036
346
c ACT134 Acute Liver Failure 44 0.036
347
PRC013 Pericarditis 44 0.036
348
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 43 0.036
349
NRT004 Neuritis 43 0.036
350
TRM010 Traumatic Brain Injury 43 0.036
351
OPT009 Optic Neuritis 43 0.036
352
GST050 Gastrointestinal System Disease 43 0.036
353
P RNV001 Renovascular Hypertension 43 0.036
354
FCT001 Factor Viii Deficiency 42 0.036
355
ACT055 Actinomycosis 41 0.036
356
SPN035 Spindle Cell Sarcoma 41 0.036
357
RDC002 Radiculopathy 41 0.036
358
FSC004 Fasciitis 40 0.036
359
NRN002 Neuronitis 40 0.036
360
CHL004 Cholelithiasis 40 0.036
361
LMB062 Limb Ischemia 38 0.036
362
CCN002 Cocaine Abuse 38 0.036
363
VRC001 Varicocele 36 0.036
364
SCR015 Scarlet Fever 36 0.036
365
IRN002 Iron Metabolism Disease 36 0.036
366
P PLN008 Peeling Skin Syndrome 36 0.036
367
MSN003 Mesenteric Vascular Occlusion 35 0.036
368
c HMG003 Hemoglobin E Disease 35 0.036
369
c SYS043 Systemic Lupus Erythematosus 1 34 0.036
370
CRT012 Cortical Blindness 32 0.036
371
BRS090 Breast Reconstruction 32 0.036
372
BCK006 Back Pain 32 0.036
373
ESP002 Esophageal Varix 30 0.036
374
c THR090 Thrombocythemia 1 30 0.036
375
c THR037 Thrombocytopenia 2 28 0.036
376
WTH001 Withdrawal Disorder 27 0.036
377
VNF001 Vein of Galen Aneurysm 26 0.036
378
THR067 Thrombophilia Due to Protein C Deficiency, Autosomal Dominant 25 0.036
379
THR089 Thrombophilia Due to Protein S Deficiency, Autosomal Dominant 24 0.036
380
c PRT045 Prothrombin-Related Thrombophilia 23 0.036
381
MTH027 Mthfr Deficiency 21 0.036
382
c BNG076 Benign Exophthalmos Syndrome 21 0.036
383
HMC030 Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency 19 0.036
384
MTH044 Mthfr Gene Mutation 17 0.036
385
P ACT061 Acute Sphenoidal Sinusitis 15 0.036
386
SNG003 Single Ventricular Heart 14 0.036
387
VSC001 Vascular Myelopathy 13 0.036
388
c CRN172 Coronary Heart Disease 3 9 0.036
389
c CRN173 Coronary Heart Disease 8 9 0.036
390
P CLR023 Colorectal Cancer 95 0.032
391
P RHM011 Rheumatoid Arthritis 88 0.032
392
P PNC035 Pancreatic Cancer 78 0.032
393
MLR004 Malaria 72 0.032
394
P CLC005 Celiac Disease 69 0.032
395
P FML161 Familial Mediterranean Fever, Ar 67 0.032
396
P PSR002 Psoriasis 64 0.032
397
c LKM062 Leukemia, Acute Lymphoblastic 63 0.032
398
DWN001 Down Syndrome 62 0.032
399
P END044 Endometriosis 61 0.032
400
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 60 0.032
401
c HPT073 Hepatitis C Virus 60 0.032
402
c PNC108 Pancreatitis, Hereditary 59 0.032
403
WLL001 Williams-Beuren Syndrome 59 0.032
404
GST092 Gastroesophageal Reflux 58 0.032
405
P RTH001 Rothmund-Thomson Syndrome 57 0.032
406
P BCL006 B-Cell Lymphomas 57 0.032
407
CHL065 Cholangiocarcinoma 56 0.032
408
c ATM010 Autoimmune Hemolytic Anemia 56 0.032
409
P PRM006 Primary Biliary Cirrhosis 56 0.032
410
LPT001 Leptospirosis 55 0.032
411
P MYM002 Moyamoya Disease 55 0.032
412
SMT008 Smith-Magenis Syndrome 54 0.032
413
WST001 West Syndrome 54 0.032
414
CRB037 Cerebral Palsy 54 0.032
415
MLN008 Melanoma 54 0.032
416
HNT002 Hantavirus Pulmonary Syndrome 52 0.032
417
GSG001 Gas Gangrene 51 0.032
418
P GRV001 Graves' Disease 51 0.032
419
P CMP010 Complex Regional Pain Syndrome 51 0.032
420
OST003 Osteonecrosis 50 0.032
421
VRL011 Viral Infectious Disease 50 0.032
422
P CNJ013 Conjunctivitis 50 0.032
423
HYD012 Hydrops Fetalis 50 0.032
424
P ART023 Arthropathy 50 0.032
425
HYP056 Hypoglycemia 49 0.032
426
MCR088 Microscopic Polyangiitis 49 0.032
427
CHC001 Chickenpox 49 0.032
428
P THY032 Thyroiditis 48 0.032
429
P SZR006 Seizure Disorder 48 0.032
430
INT002 Intermittent Claudication 48 0.032
431
P ENC004 Encephalitis 48 0.032
432
LYM040 Lymphoblastic Lymphoma 48 0.032
433
PHR003 Pharyngitis 48 0.032
434
P LYM025 Lymphedema 48 0.032
435
WLL006 Wells Syndrome 48 0.032
436
LYM021 Lymphadenitis 48 0.032
437
HYP080 Hypogonadism 47 0.032
438
MRB003 Morbid Obesity 47 0.032
439
THR100 Thrombocytopenic Purpura, Autoimmune 47 0.032
440
SPT004 Septic Arthritis 47 0.032
441
P PRC031 Preeclampsia/eclampsia 1 47 0.032
442
P ORL007 Oral Cavity Cancer 47 0.032
443
c HPT003 Hepatitis a 47 0.032
444
PYD001 Pyoderma Gangrenosum 46 0.032
445
c MLG069 Malignant Hypertension 46 0.032
446
PLS011 Plasmacytoma 46 0.032
447
c INF069 Infantile Neuroaxonal Dystrophy 1 46 0.032
448
P MST018 Mesothelioma 45 0.032
449
UTR039 Uterine Fibroid 45 0.032
450
HMT018 Hematopoietic Stem Cell Transplantation 45 0.032
451
PLM010 Pulmonary Edema 45 0.032
452
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 44 0.032
453
ART031 Aortic Coarctation 44 0.032
454
URM002 Uremia 44 0.032
455
CRN036 Craniopharyngioma 44 0.032
456
END021 Endomyocardial Fibrosis 44 0.032
457
P EXP004 Exophthalmos 44 0.032
458
TRC023 Trichinosis 43 0.032
459
P GST049 Gastrointestinal System Cancer 43 0.032
460
CHR074 Choriocarcinoma 43 0.032
461
TRN015 Transient Cerebral Ischemia 43 0.032
462
IPX001 Ipex Syndrome 43 0.032
463
MYH001 May-Hegglin Anomaly 43 0.032
464
HYP266 Hypoxia 42 0.032
465
CRT016 Carotid Artery Disease 42 0.032
466
NDL013 Nodular Regenerative Hyperplasia 42 0.032
467
INF034 Infective Endocarditis 42 0.032
468
CMR002 Coumarin Resistance 42 0.032
469
PRS045 Prostatic Hypertrophy 41 0.032
470
HNC001 Henoch-Schoenlein Purpura 41 0.032
471
VNW005 Von Willebrand Disease, Type 1 41 0.032
472
GST053 Gastric Cancer 41 0.032
473
P PNC001 Pancytopenia 41 0.032
474
PYD002 Pyoderma 41 0.032
475
ANG018 Angiomyolipoma 40 0.032
476
PLC007 Placental Abruption 40 0.032
477
BNF002 Bone Fracture 39 0.032
478
TRN012 Transient Global Amnesia 39 0.032
479
ART004 Aortic Atherosclerosis 39 0.032
480
P CHL066 Cholangitis 39 0.032
481
FCT005 Factor Xiii Deficiency 39 0.032
482
MYL001 Myelitis 39 0.032
483
ESN011 Eisenmenger Syndrome 38 0.032
484
HST009 Histiocytoma 38 0.032
485
NRR001 Neuroretinitis 38 0.032
486
c ACT042 Acute Pyelonephritis 38 0.032
487
RTN021 Retinal Vascular Occlusion 38 0.032
488
HRM002 Hermaphroditism 37 0.032
489
KLT001 Klatskin's Tumor 37 0.032
490
GDS001 Good Syndrome 37 0.032
491
VTM002 Vitamin B12 Deficiency 37 0.032
492
SDD007 Sudden Cardiac Death 36 0.032
493
P CMP008 Compartment Syndrome 36 0.032
494
RSP006 Respiratory System Disease 36 0.032
495
PLV005 Pelviureteric Junction Obstruction 36 0.032
496
INT221 Intravascular Large B-Cell Lymphoma 35 0.032
497
P HMR005 Hemorrhoid 35 0.032
498
c CNT028 Central Retinal Artery Occlusion 34 0.032
499
URN009 Urinary System Disease 33 0.032
500
ISC015 Ischemic Colitis 33 0.032
501
PNM013 Pneumococcal Meningitis 33 0.032
502
BRN026 Branch Retinal Artery Occlusion 33 0.032
503
P LBY004 Labyrinthitis 32 0.032
504
LVD002 Livedoid Vasculopathy 32 0.032
505
STR044 Steroid-Resistant Nephrotic Syndrome 31 0.032
506
CHL070 Cholesterol Embolism 31 0.032
507
BSL004 Basilar Artery Occlusion 31 0.032
508
INF013 Inferior Myocardial Infarction 31 0.032
509
PRP019 Peripheral Nervous System Disease 31 0.032
510
GST071 Gastrointestinal Carcinoma 31 0.032
511
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 30 0.032
512
CHR084 Chromosomal Disease 30 0.032
513
FRN014 Fournier Gangrene 29 0.032
514
GNT005 Giant Hemangioma 29 0.032
515
EPD005 Epidural Abscess 29 0.032
516
GND003 Gonadal Disease 28 0.032
517
ANT013 Anterior Spinal Artery Syndrome 28 0.032
518
INF133 Inferior Vena Cava Interruption 26 0.032
519
c PLN018 Peeling Skin Syndrome 2 25 0.032
520
SPC003 Specific Developmental Disorder 25 0.032
521
c INH004 Inherited Blood Coagulation Disease 25 0.032
522
P ERY048 Erythrocytosis, Familial, 2 25 0.032
523
IMP003 Impaired Renal Function Disease 23 0.032
524
THR068 Thrombophilia Due to Protein C Deficiency, Autosomal Recessive 23 0.032
525
ABD009 Abducens Palsy 20 0.032
526
P ACT080 Acute Pulmonary Heart Disease 20 0.032
527
c THR102 Thrombocytopenia 5 19 0.032
528
CRB031 Cerebral Arterial Disease 19 0.032
529
OCL041 Oculomotor Apraxia Cogan Type 17 0.032
530
DBL009 Double Inferior Vena Cava 16 0.032
531
PRN017 Perianal Hematoma 14 0.032
532
HRD147 Hereditary Thrombophilia Due to Congenital Protein S Deficiency 12 0.032
533
WRF003 Warfarin Syndrome 12 0.032
534
c ANT041 Antiphospholipid Syndrome, Familial 12 0.032
535
NNT044 Neonatal Antiphospholipid Syndrome 12 0.032
536
c RNL016 Renal Infectious Disease 7 0.032
537
WSC001 Wisconsin Syndrome 4 0.032
538
DWS002 Dawson Disease 3 0.032
539
CYS001 Cystic Fibrosis 90 0.026
540
P RTT002 Rett Syndrome 79 0.026
541
P HYP607 Hypercholesterolemia, Familial 79 0.026
542
HV1006 Hiv-1 77 0.026
543
c CHR090 Chronic Lymphocytic Leukemia 70 0.026
544
P MDL005 Medulloblastoma 69 0.026
545
P OVR042 Ovarian Cancer 69 0.026
546
P CSH001 Cushing's Syndrome 67 0.026
547
P RBN001 Rubinstein-Taybi Syndrome 66 0.026
548
P NRF002 Neurofibromatosis 66 0.026
549
P TBR001 Tuberous Sclerosis 65 0.026
550
P FML011 Familial Adenomatous Polyposis 65 0.026
551
c NRF018 Neurofibromatosis, Type 1 63 0.026
552
P HRM001 Hermansky-Pudlak Syndrome 62 0.026
553
P LKM068 Leukemia, Chronic Myeloid, Somatic 62 0.026
554
OBS002 Obsessive-Compulsive Disorder 62 0.026
555
c CHR089 Chronic Kidney Failure 61 0.026
556
P ALX003 Alexander Disease 61 0.026
557
P KDN017 Kidney Cancer 60 0.026
558
P DYS007 Dyskeratosis Congenita 60 0.026
559
P AMY004 Amyloidosis 60 0.026
560
P PLY014 Polycystic Kidney Disease 60 0.026
561
CYS010 Cystinosis 59 0.026
562
MSM014 Mismatch Repair Cancer Syndrome 58 0.026
563
FCT003 Factor X Deficiency 58 0.026
564
P DRM010 Dermatomyositis 57 0.026
565
MLG056 Malignant Hyperthermia 56 0.026
566
P HYP117 Hypertriglyceridemia 56 0.026
567
c SYS004 Systemic Mastocytosis 56 0.026
568
P AST007 Astrocytoma 55 0.026
569
CHR081 Choroideremia 55 0.026
570
BRC012 Brucellosis 55 0.026
571
P HMN010 Hemangioma 54 0.026
572
DRM006 Dermatitis 54 0.026
573
ADN018 Adenoma 54 0.026
574
EYD002 Eye Disease 54 0.026
575
c FML001 Familial Atrial Fibrillation 53 0.026
576
P CNG001 Congenital Myasthenic Syndrome 53 0.026
577
ADL030 Adult-Onset Still's Disease 53 0.026
578
KLP010 Klippel-Trenaunay-Weber Syndrome 53 0.026
579
P HYP086 Hypothyroidism 52 0.026
580
LGG001 Legg-Calve-Perthes Disease 52 0.026
581
P MSC005 Muscular Dystrophy 52 0.026
582
c ACT210 Acute Respiratory Distress Syndrome 52 0.026
583
P PRD008 Periodontitis 52 0.026
584
P HYP620 Hypoprothrombinemia 52 0.026
585
DBN001 Dubin-Johnson Syndrome 52 0.026
586
P ANR007 Anorexia Nervosa 52 0.026
587
c CNT035 Central Nervous System Disease 52 0.026
588
END030 End Stage Renal Failure 51 0.026
589
RHB003 Rhabdomyosarcoma 51 0.026
590
P EHL001 Ehlers-Danlos Syndrome 51 0.026
591
PMS001 Poems Syndrome 51 0.026
592
ECH003 Echinococcosis 51 0.026
593
NTH001 Netherton Syndrome 51 0.026
594
VSC044 Visceral Myopathy 51 0.026
595
ALV002 Alveolar Echinococcosis 50 0.026
596
ATP002 Atopy 50 0.026
597
P MYP004 Myopathy 50 0.026
598
P RBL001 Rubella 50 0.026
599
c VRL010 Viral Hepatitis 49 0.026
600
P NRV007 Nervous System Disease 49 0.026
601
CNN005 Connective Tissue Disease 49 0.026
602
P APL006 Aplasia Cutis Congenita 49 0.026
603
P LPS002 Liposarcoma 49 0.026
604
P PLY017 Polyarteritis Nodosa 49 0.026
605
CYS005 Cysticercosis 49 0.026
606
NTR040 Neutropenia, Cyclic 49 0.026
607
TXC005 Toxic Shock Syndrome 49 0.026
608
MGR028 Migraine with or Without Aura 1 49 0.026
609
c HPT015 Hepatitis D 48 0.026
610
c PRM012 Primary Polycythemia 48 0.026
611
P CYS036 Cystinosis, Nephropathic 48 0.026
612
P CTR002 Cataract 48 0.026
613
P MST009 Mastocytosis 48 0.026
614
P MYC008 Myocarditis 47 0.026
615
GNG013 Gingivitis 47 0.026
616
P THR003 Thoracic Aortic Aneurysm 47 0.026
617
FCT022 Factor Xi Deficiency, Autosomal Recessive 47 0.026
618
SLP005 Sleep Disorder 47 0.026
619
TNS005 Tonsillitis 47 0.026
620
PLV003 Pelvic Inflammatory Disease 47 0.026
621
P ANP001 Anaplastic Large Cell Lymphoma 47 0.026
622
CGN006 Cogan Syndrome 46 0.026
623
CRN014 Cronkhite-Canada Syndrome 46 0.026
624
OBS061 Obstructive Sleep Apnea 46 0.026
625
P DBT005 Diabetes Insipidus 46 0.026
626
STS002 Situs Inversus 46 0.026
627
P FML035 Familial Hyperlipidemia 46 0.026
628
P ENC008 Encephalocele 46 0.026
629
MYC002 Mycobacterium Avium Complex Disease 46 0.026
630
P MNC007 Monocytic Leukemia 45 0.026
631
c ACT071 Acute Kidney Failure 45 0.026
632
P PLY041 Polymyositis 45 0.026
633
BLD034 Bile Duct Carcinoma 45 0.026
634
CRY004 Cryoglobulinemia 45 0.026
635
CTN014 Cutaneous Mastocytosis 45 0.026
636
c BCT007 Bacterial Meningitis 45 0.026
637
MGC001 Megacolon 45 0.026
638
END031 Endometrial Stromal Sarcoma 45 0.026
639
P INT068 Intestinal Disease 44 0.026
640
P HYP060 Hyperinsulinism 44 0.026
641
CTY001 Cat Eye Syndrome 44 0.026
642
P EPS003 Episodic Ataxia 44 0.026
643
P OVR049 Ovarian Disease 44 0.026
644
ART002 Arts Syndrome 44 0.026
645
INT079 Intrahepatic Cholangiocarcinoma 44 0.026
646
HMR039 Hemorrhage, Intracerebral 44 0.026
647
PRN011 Pernicious Anemia 44 0.026
648
ESP023 Esophageal Disease 44 0.026
649
ASP003 Aseptic Meningitis 44 0.026
650
c MLG002 Malignant Peritoneal Mesothelioma 44 0.026
651
CLS010 Cluster Headache 44 0.026
652
P CRV031 Cervical Adenocarcinoma 44 0.026
653
GST040 Gastric Adenocarcinoma 44 0.026
654
P HMR012 Hemorrhagic Fever 44 0.026
655
P PRT096 Peritoneal Mesothelioma 44 0.026
656
P OPH004 Ophthalmoplegia 43 0.026
657
PRT012 Prothrombin Deficiency 43 0.026
658
SCT005 Scott Syndrome 43 0.026
659
CVR006 Cavernous Hemangioma 43 0.026
660
FCL012 Facial Paralysis 43 0.026
661
HMP005 Hemiplegia 43 0.026
662
P HYD002 Hydronephrosis 42 0.026
663
P PRN026 Porencephaly 42 0.026
664
UTR024 Uterine Carcinosarcoma 42 0.026
665
P SHR001 Short Bowel Syndrome 42 0.026
666
EBS001 Ebstein Anomaly 42 0.026
667
P MGR003 Migraine with Aura 41 0.026
668
P NNT009 Neonatal Diabetes Mellitus 41 0.026
669
PRC012 Pericardial Effusion 41 0.026
670
NTR005 Nutritional Deficiency Disease 41 0.026
671
P GND004 Gonadal Dysgenesis 41 0.026
672
LFT009 Left Ventricular Outflow Tract Obstruction 41 0.026
673
MCN001 Mucinous Adenocarcinoma 41 0.026
674
OBS001 Obstructive Jaundice 40 0.026
675
SMN007 Seminoma 40 0.026
676
P TRN034 Transverse Myelitis 40 0.026
677
JNT002 Joint Disorders 39 0.026
678
MNT002 Mental Depression 39 0.026
679
OPT006 Optic Nerve Disease 39 0.026
680
P SYR001 Syringomyelia 39 0.026
681
MNN014 Mononeuritis 39 0.026
682
P END047 Endophthalmitis 39 0.026
683
NCR007 Necrotizing Fasciitis 39 0.026
684
EBL001 Ebola Hemorrhagic Fever 38 0.026
685
RNL015 Renal Hypertension 38 0.026
686
URT010 Ureteral Obstruction 38 0.026
687
PRN021 Paranasal Sinus Disease 38 0.026
688
SPL004 Splenic Marginal Zone Lymphoma 38 0.026
689
CLL002 Collecting Duct Carcinoma 38 0.026
690
c ACQ014 Acquired Hemophilia 37 0.026
691
HPT008 Hepatic Tuberculosis 37 0.026
692
CNV002 Conversion Disorder 37 0.026
693
BRN080 Brain Ischemia 37 0.026
694
HYP143 Hypomyelination and Congenital Cataract 37 0.026
695
SPR007 Superior Mesenteric Artery Syndrome 37 0.026
696
c SVR056 Severe Hemophilia a 37 0.026
697
HMC006 Homocystinuria Due to Mthfr Deficiency 36 0.026
698
P OVR046 Ovarian Cyst 36 0.026
699
c HMG001 Hemoglobin C Disease 36 0.026
700
MYX006 Myxoid Leiomyosarcoma 36 0.026
701
ADN027 Adenomyosis 36 0.026
702
LMY003 Leiomyomatosis 36 0.026
703
STM006 Stomach Disease 36 0.026
704
ALX001 Alexia 36 0.026
705
P HRN001 Horner's Syndrome 36 0.026
706
IDP033 Idiopathic Edema 36 0.026
707
CRR007 Cirrhosis, Cryptogenic 36 0.026
708
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 36 0.026
709
P NRL007 Neurologic Diseases 35 0.026
710
MYS004 Myiasis 35 0.026
711
KRN001 Korean Hemorrhagic Fever 35 0.026
712
HMN016 Hemangioendothelioma 35 0.026
713
TRN007 Transsexualism 35 0.026
714
TTL010 Total Anomalous Pulmonary Venous Return 35 0.026
715
ADS002 Adie Syndrome 34 0.026
716
CRT008 Carotid Artery Dissection 34 0.026
717
UPP004 Upper Respiratory Tract Disease 34 0.026
718
SPL018 Splenomegaly 34 0.026
719
VRT001 Vertebral Artery Occlusion 33 0.026
720
CNS002 Constrictive Pericarditis 33 0.026
721
BLR015 Blue Rubber Bleb Nevus Syndrome 33 0.026
722
PHY002 Physical Disorder 33 0.026
723
MNN021 Meningococcemia 33 0.026
724
c ACQ042 Acquired Hemophilia a 33 0.026
725
INT253 Intestinal Benign Neoplasm 33 0.026
726
c SBC003 Subacute Bacterial Endocarditis 33 0.026
727
P CRN035 Cranial Nerve Palsy 33 0.026
728
STR077 Streptococcal Toxic-Shock Syndrome 33 0.026
729
LYM014 Lymphangitis 33 0.026
730
MRN001 Marantic Endocarditis 33 0.026
731
c MTR002 Mitral Valve Insufficiency 32 0.026
732
HPT004 Hepatic Coma 32 0.026
733
LYM005 Lymphocele 32 0.026
734
MCR225 Macrophage Activation Syndrome 32 0.026
735
CPL011 Capillary Malformations, Congenital, 1, Somatic, Mosaic 32 0.026
736
CRN020 Coronary Restenosis 31 0.026
737
CNN002 Cannabis Abuse 31 0.026
738
BLT003 Blue Toe Syndrome 31 0.026
739
PLY004 Polyp of Corpus Uteri 31 0.026
740
PRP028 Peripheral Vertigo 31 0.026
741
VSL002 Visual Epilepsy 31 0.026
742
MLK004 Malakoplakia 30 0.026
743
P ATM020 Autoimmune Enteropathy 30 0.026
744
HPT074 Hepatic Adenoma, Somatic 30 0.026
745
AMR003 Amaurosis Fugax 30 0.026
746
BWN002 Bowen Syndrome 30 0.026
747
SCT001 Sciatic Neuropathy 30 0.026
748
QLT001 Qualitative Platelet Defect 30 0.026
749
FMR003 Femoral Neuropathy 30 0.026
750
ETH009 Ethmoid Sinusitis 30 0.026
751
HYP319 Hypereosinophilic Syndrome, Idiopathic, Resistant to Imatinib 30 0.026
752
ART110 Arteritic Anterior Ischemic Optic Neuropathy 30 0.026
753
c ACT036 Acute Cholangitis 29 0.026
754
PRM008 Parametritis 29 0.026
755
LCH001 Leech Infestation 29 0.026
756
BND014 Bone Development Disease 28 0.026
757
c PSR017 Psoriasis 2 28 0.026
758
P PSR004 Psoriasis Susceptibility 1 28 0.026
759
LNG095 Lung Abscess 28 0.026
760
NSL022 Nasal Cavity Disease 28 0.026
761
c CTR103 Cataract 4, Multiple Types 28 0.026
762
SBN001 Subendocardial Myocardial Infarction 28 0.026
763
FML039 Female Reproductive System Disease 28 0.026
764
TFT003 Tufting Enteropathy 27 0.026
765
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 27 0.026
766
HNM002 Hinman Syndrome 27 0.026
767
PRG092 Pregnancy Loss, Recurrent 1 27 0.026
768
PRM025 Primary Bacterial Infectious Disease 27 0.026
769
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 27 0.026
770
c LKD009 Leukodystrophy, Hypomyelinating, 5 26 0.026
771
P PRX010 Paroxysmal Ventricular Fibrillation 26 0.026
772
RPR002 Reproductive System Disease 26 0.026
773
TXC001 Toxic Megacolon 25 0.026
774
MNN005 Meningovascular Neurosyphilis 25 0.026
775
CLS041 Classic Homocystinuria 25 0.026
776
FBR028 Fibrosing Mediastinitis 25 0.026
777
CTR009 Cataract Congenital Dominant Non Nuclear 25 0.026
778
HNS001 Hansen's Disease 25 0.026
779
SRN001 Serine Deficiency 25 0.026
780
GLY032 Glycosylphosphatidylinositol Deficiency 25 0.026
781
P IGN003 Iga Nephropathy 1 24 0.026
782
c PSR019 Psoriasis Susceptibility 13 23 0.026
783
c PLN017 Peeling Skin Syndrome 1 23 0.026
784
MTH028 Mthfr Thermolabile Variant 23 0.026
785
GRN008 Granular Cell Carcinoma 23 0.026
786
DNT046 Dental Abscess 23 0.026
787
MTR013 Motor Neuritis 23 0.026
788
WND002 Wandering Spleen 23 0.026
789
INT050 Intestinal Impaction 22 0.026
790
BNP002 Bone Epithelioid Hemangioma 22 0.026
791
NRS005 Neurosarcoidosis 22 0.026
792
GLB003 Globe Disease 22 0.026
793
P FML187 Familial Hypertension 21 0.026
794
PRX023 Paroxysmal Nocturnal Hemoglobinuria, Somatic 21 0.026
795
PRR008 Periarteritis Nodosa 21 0.026
796
CNG453 Congenital Factor Vii Deficiency 21 0.026
797
PSR005 Psoriasis, Protection Against 21 0.026
798
BRW006 Brown Syndrome 20 0.026
799
c ACT035 Acute Frontal Sinusitis 19 0.026
800
AND005 Androgen Insensitivity Syndrome, Mild 19 0.026
801
THR007 Thrombophlebitis Migrans 18 0.026
802
THR021 Thrombophilia Due to Hrg Deficiency 18 0.026
803
CRD023 Cardiomyopathy Cataract Hip Spine Disease 17 0.026
804
PRT006 Partial Motor Epilepsy 17 0.026
805
THR020 Thrombophilia Due to Heparin Cofactor Ii Deficiency 17 0.026
806
YNG002 Young Syndrome 16 0.026
807
c PLN021 Peeling Skin Syndrome 3 16 0.026
808
CRB017 Cerebral Falx Meningioma 16 0.026
809
CRB087 Cerebral Arteriosclerosis 14 0.026
810
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 13 0.026
811
OCL024 Ocular Neuromyotonia 13 0.026
812
ACT174 Acute Peripheral Arterial Occlusion 13 0.026
813
CRT056 Carotidynia 12 0.026
814
c BLR016 Biliary Cirrhosis, Primary, 2 10 0.026
815
c BLR026 Biliary Cirrhosis, Primary, 5 10 0.026
816
VSC009 Vascular Skin Disease 9 0.026
817
BWM001 Bowman's Membrane Folds or Rupture 7 0.026
818
GNT013 Genetic Brain Disorders 3 0.026
819
P ALZ034 Alzheimer Disease 98 0.018
820
P PRS040 Prostate Cancer 90 0.018
821
c AMY091 Amyotrophic Lateral Sclerosis 1 83 0.018
822
P OST012 Osteoarthritis 79 0.018
823
P LFR001 Li-Fraumeni Syndrome 79 0.018
824
DCH001 Duchenne Muscular Dystrophy 78 0.018
825
HDG012 Hodgkin Lymphoma 75 0.018
826
FBR012 Fabry Disease 75 0.018
827
P HMC003 Hemochromatosis 75 0.018
828
P HRD008 Hereditary Hemorrhagic Telangiectasia 74 0.018
829
c LKM061 Leukemia, Acute Myeloid 74 0.018
830
c DLT002 Dilated Cardiomyopathy 73 0.018
831
P NRB001 Neuroblastoma 73 0.018
832
ADN021 Adenomatous Polyposis Coli 71 0.018
833
c FNC027 Fanconi Anemia, Complementation Group a 71 0.018
834
P OST005 Osteogenesis Imperfecta 70 0.018
835
PRP003 Porphyria Cutanea Tarda 69 0.018
836
ESP021 Esophageal Cancer 69 0.018
837
P SCL016 Scleroderma 69 0.018
838
P WSK001 Wiskott-Aldrich Syndrome 68 0.018
839
P BRD002 Bardet-Biedl Syndrome 68 0.018
840
PTZ001 Peutz-Jeghers Syndrome 67 0.018
841
END057 Endometrial Cancer 67 0.018
842
GLL008 Gilles De La Tourette Syndrome 67 0.018
843
P PRM019 Premature Ovarian Failure 66 0.018
844
BCK001 Becker Muscular Dystrophy 66 0.018
845
P DMN001 Diamond-Blackfan Anemia 66 0.018
846
P STH001 Saethre-Chotzen Syndrome 65 0.018
847
SVR004 Severe Combined Immunodeficiency 65 0.018
848
LSC001 Lesch-Nyhan Syndrome 64 0.018
849
P INF038 Influenza 64 0.018
850
P STM004 Stomach Cancer 63 0.018
851
BLM001 Bloom Syndrome 63 0.018
852
P PRD006 Prader-Willi Syndrome 62 0.018
853
ORN006 Ornithine Transcarbamylase Deficiency 61 0.018
854
MLD001 Melioidosis 61 0.018
855
CHD001 Chediak-Higashi Syndrome 61 0.018
856
SKN016 Skin Disease 61 0.018
857
P LYM007 Lymphangioleiomyomatosis 61 0.018
858
P ADD001 Addison's Disease 60 0.018
859
P HRP006 Herpes Simplex 60 0.018
860
CNT098 Central Core Disease 60 0.018
861
PLM001 Pulmonary Tuberculosis 60 0.018
862
TST021 Testicular Germ Cell Tumor 60 0.018
863
P HRS035 Hirschsprung Disease 1 59 0.018
864
c BRD010 Bardet-Biedl Syndrome 1 59 0.018
865
WGN006 Wegener Granulomatosis 59 0.018
866
P HMP002 Hemophagocytic Lymphohistiocytosis 59 0.018
867
ARG002 Argininosuccinic Aciduria 59 0.018
868
P CNT061 Conotruncal Heart Malformations 59 0.018
869
ALC007 Alcohol Dependence 59 0.018
870
ACR008 Acrocallosal Syndrome 58 0.018
871
P PLY011 Polycystic Ovary Syndrome 58 0.018
872
P SLV001 Silver-Russell Syndrome 58 0.018
873
P SPN046 Spinal Muscular Atrophy 58 0.018
874
c MYT021 Myotonic Dystrophy 1 58 0.018
875
P ATP001 Atopic Dermatitis 57 0.018
876
c ATM003 Autoimmune Thyroiditis 57 0.018
877
c CNG006 Congenital Hypothyroidism 57 0.018
878
DNG003 Dengue Disease 57 0.018
879
P CRB042 Cerebellar Ataxia 56 0.018
880
DBT088 Diabetes Insipidus, Nephrogenic 56 0.018
881
P HYP061 Hypertrophic Cardiomyopathy 56 0.018
882
P ADL010 Adult Respiratory Distress Syndrome 55 0.018
883
ARS001 Aarskog-Scott Syndrome 55 0.018
884
DNG002 Dengue Hemorrhagic Fever 55 0.018
885
c MNN043 Meningioma, Familial 55 0.018
886
c MCL062 Mucolipidosis Ii Alpha/beta 55 0.018
887
P MYS005 Myositis 54 0.018
888
HRP004 Herpes Zoster 54 0.018
889
CCC001 Coccidioidomycosis 54 0.018
890
PRP032 Porphyria Variegata 54 0.018
891
P SJG001 Sjogren's Syndrome 54 0.018
892
P LDD002 Liddle Syndrome 54 0.018
893
P PRP029 Porphyria 54 0.018
894
P SCH018 Schizencephaly 54 0.018
895
CRT002 Cartilage-Hair Hypoplasia 53 0.018
896
FRB001 Farber Lipogranulomatosis 53 0.018
897
GRY002 Gray Platelet Syndrome 53 0.018
898
P GLB002 Glioblastoma 53 0.018
899
MXD005 Mixed Connective Tissue Disease 53 0.018
900
IRR002 Irritable Bowel Syndrome 53 0.018
901
LGN002 Legionellosis 53 0.018
902
CHR020 Chronic Interstitial Cystitis 53 0.018
903
c EPL070 Epilepsy, Progressive Myoclonic 2b 52 0.018
904
GLB015 Glioblastoma Multiforme 52 0.018
905
P CHN012 Chondrosarcoma 52 0.018
906
OLL001 Ollier Disease 52 0.018
907
P INF032 Infertility 52 0.018
908
P GLY010 Glycine Encephalopathy 52 0.018
909
P ALP009 Alopecia Areata 52 0.018
910
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 52 0.018
911
c OST135 Osteogenesis Imperfecta, Type I 51 0.018
912
STT001 Status Epilepticus 51 0.018
913
P ADM011 Adams-Oliver Syndrome 51 0.018
914
P ICH001 Ichthyosis Vulgaris 51 0.018
915
P RTN025 Retinoschisis 51 0.018
916
TST014 Testicular Cancer 51 0.018
917
ICH002 Ichthyosis Bullosa of Siemens 51 0.018
918
c ATM002 Autoimmune Polyendocrine Syndrome Type 1 50 0.018
919
P ERY008 Erythromelalgia 50 0.018
920
P VNT002 Ventricular Septal Defect 50 0.018
921
CHL014 Cholera 50 0.018
922
MLL005 Miller-Dieker Syndrome 50 0.018
923
c CRB103 Cerebral Cavernous Malformations-1 50 0.018
924
BNC003 Bone Cancer 50 0.018
925
BBS001 Babesiosis 50 0.018
926
CHN016 Cohen Syndrome 49 0.018
927
SPT005 Spotted Fever 49 0.018
928
P MCR010 Microcephaly 49 0.018
929
CMP002 Campylobacteriosis 49 0.018
930
P PLY006 Polydactyly 49 0.018
931
P GST044 Gastritis 49 0.018
932
ACT049 Acute Disseminated Encephalomyelitis 49 0.018
933
LKM067 Leukemia, Acute Promyelocytic, Somatic 49 0.018
934
ATX019 Ataxia with Vitamin E Deficiency 49 0.018
935
PLM034 Pulmonary Emphysema 49 0.018
936
GLC003 Glucose Intolerance 49 0.018
937
FTT001 Fatty Liver Disease 49 0.018
938
BRK001 Brooke-Spiegler Syndrome 49 0.018
939
CNG048 Congenital Hepatic Fibrosis 49 0.018
940
KRT002 Keratomalacia 49 0.018
941
JCB001 Jacobsen Syndrome 49 0.018
942
LMY002 Leiomyoma 49 0.018
943
FLL026 Fallopian Tube Cancer 49 0.018
944
HPT022 Hepatoblastoma 49 0.018
945
P UVT001 Uveitis 49 0.018
946
ETH011 Ethylmalonic Encephalopathy 48 0.018
947
JPN002 Japanese Encephalitis 48 0.018
948
PTT046 Pituitary Hormone Deficiency, Combined, 2 48 0.018
949
ERD001 Erdheim-Chester Disease 48 0.018
950
SFT003 Soft Tissue Sarcoma 48 0.018
951
P FNG005 Feingold Syndrome 48 0.018
952
AMN001 Amenorrhea 48 0.018
953
P OLG002 Oligodendroglioma 48 0.018
954
NRT001 Neurotic Disorder 48 0.018
955
P HYP050 Hyperinsulinemic Hypoglycemia 48 0.018
956
INT146 Intervertebral Disc Disease 48 0.018
957
c MLG077 Malignant Peripheral Nerve Sheath Tumor 48 0.018
958
c SCN006 Secondary Syphilis 48 0.018
959
GST060 Gastric Cancer, Somatic 48 0.018
960
PRT002 Paratyphoid Fever 47 0.018
961
END041 Endometrial Adenocarcinoma 47 0.018
962
MFF001 Maffucci Syndrome 47 0.018
963
PPT005 Peptic Ulcer Disease 47 0.018
964
GTR002 Goiter 47 0.018
965
c PRM126 Primary Peritoneal Carcinoma 47 0.018
966
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 47 0.018
967
P MCR115 Microvascular Complications of Diabetes 5 47 0.018
968
LPR001 Lepromatous Leprosy 47 0.018
969
RNL024 Renal Glucosuria 47 0.018
970
ACS001 Acoustic Neuroma 47 0.018
971
P RNL028 Renal Tubular Dysgenesis 47 0.018
972
P STR020 Strabismus 47 0.018
973
c AFB002 Afibrinogenemia, Congenital 46 0.018
974
P FNC004 Fanconi Syndrome 46 0.018
975
CCT002 Cicatricial Pemphigoid 46 0.018
976
SCR008 Scrub Typhus 46 0.018
977
P SPR013 Spiradenoma 46 0.018
978
TSC001 Tsc2 Angiomyolipomas, Renal, Modifier of 46 0.018
979
RTN018 Retinal Disease 46 0.018
980
RNL007 Renal Tubular Acidosis 46 0.018
981
GST037 Gastroparesis 46 0.018
982
P CRP007 Carpenter Syndrome 46 0.018
983
PRD019 Periodic Fever, Familial 46 0.018
984
P ANG015 Angioedema 46 0.018
985
LYS002 Lysosomal Storage Disease 46 0.018
986
GLC085 Glucose-6-Phosphate Dehydrogenase Deficiency 46 0.018
987
ZLL002 Zollinger-Ellison Syndrome 46 0.018
988
P HMN013 Hemangiopericytoma 46 0.018
989
BLL003 Bell's Palsy 46 0.018
990
c MCR113 Microvascular Complications of Diabetes 3 46 0.018
991
MTN003 Motion Sickness 45 0.018
992
P HYP065 Hyperaldosteronism 45 0.018
993
IMP002 Imperforate Anus 45 0.018
994
TYP011 Typhus 45 0.018
995
c ALM001 Al Amyloidosis 45 0.018
996
CND002 Conduct Disorder 45 0.018
997
NRM005 Neuromuscular Disease 45 0.018
998
c CNT033 Central Nervous System Cancer 45 0.018
999
PMP001 Pemphigus 45 0.018
1000
LYS001 Loeys-Dietz Syndrome 45 0.018
1001
P ZLL001 Zellweger Syndrome 45 0.018
1002
PLS009 Plasma Cell Neoplasm 45 0.018
1003
P MSC003 Muscular Atrophy 45 0.018
1004
ALD010 Aldosteronism, Glucocorticoid-Remediable 44 0.018
1005
ING001 Inguinal Hernia 44 0.018
1006
P MYS033 Miyoshi Muscular Dystrophy 1 44 0.018
1007
P UTR038 Uterine Disease 44 0.018
1008
P VSC005 Vesicoureteral Reflux 44 0.018
1009
CTS003 Coats Disease 44 0.018
1010
BLM002 Bulimia Nervosa 44 0.018
1011
c INS002 in Situ Carcinoma 44 0.018
1012
MYL020 Myelomeningocele 44 0.018
1013
CRT049 Critical Limb Ischemia 44 0.018
1014
SRS001 Serous Cystadenocarcinoma 44 0.018
1015
P NRV006 Nervous System Cancer 44 0.018
1016
P SYP003 Syphilis 44 0.018
1017
P SCL018 Scoliosis 44 0.018
1018
IMM033 Immunodeficiency Due to Purine Nucleoside Phosphorylase Deficiency 44 0.018
1019
NRN004 Neuroendocrine Tumor 44 0.018
1020
NNL002 Nonalcoholic Steatohepatitis 43 0.018
1021
c CNG415 Congenital Disorder of Glycosylation, Type Ia 43 0.018
1022
c PST041 Posterior Urethral Valves 43 0.018
1023
MMM001 Mammary Paget's Disease 43 0.018
1024
P MGS004 Meige Syndrome 43 0.018
1025
TBR006 Tuberculoid Leprosy 43 0.018
1026
P BRS044 Breast Adenocarcinoma 43 0.018
1027
MCR004 Macroglobulinemia 43 0.018
1028
RCT018 Rectal Neoplasm 43 0.018
1029
END020 Endocardial Fibroelastosis 43 0.018
1030
GST009 Gastroschisis 43 0.018
1031
DMY004 Demyelinating Disease 43 0.018
1032
c ACT009 Acute Monocytic Leukemia 43 0.018
1033
RPD002 Rapadilino Syndrome 43 0.018
1034
PLC005 Placental Insufficiency 43 0.018
1035
PNV001 Panuveitis 43 0.018
1036
c ART115 Aortic Valve Disease 1 43 0.018
1037
c TBR024 Tuberous Sclerosis-1 43 0.018
1038
P ATX004 Ataxia 43 0.018
1039
c LRG001 Large Cell Carcinoma 43 0.018
1040
MCN007 Meconium Aspiration Syndrome 43 0.018
1041
P PRV002 Periventricular Nodular Heterotopia 43 0.018
1042
ANK001 Ankylosis 43 0.018
1043
GRM005 Germ Cell Cancer 43 0.018
1044
RTC005 Reticulosarcoma 42 0.018
1045
P PLC011 Pilocytic Astrocytoma 42 0.018
1046
FBR032 Fibromuscular Dysplasia 42 0.018
1047
P PTS002 Ptosis 42 0.018
1048
OLG003 Oligohydramnios 42 0.018
1049
CRN027 Corneal Neovascularization 42 0.018
1050
NRN001 Neuroendocrine Carcinoma 42 0.018
1051
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 42 0.018
1052
ADN002 Adenoiditis 42 0.018
1053
GNT031 Genitopatellar Syndrome 42 0.018
1054
CHR031 Chromoblastomycosis 42 0.018
1055
P BRN009 Burning Mouth Syndrome 42 0.018
1056
P SCL009 Sclerosing Cholangitis 42 0.018