Search results for "thrombosis"

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

1039 hits were found for 'thrombosis'

# Family MCID Name MIFTS Score
1
SGT001 Sagittal Sinus Thrombosis 49 5.789
2
PRT018 Portal Vein Thrombosis 54 5.514
3
VNS009 Venous Thrombosis 55 5.277
4
CRN017 Coronary Thrombosis 59 5.078
5
INT078 Intracranial Thrombosis 31 4.977
6
LTR002 Lateral Sinus Thrombosis 25 4.607
7
CVR002 Cavernous Sinus Thrombosis 28 4.295
8
CRT004 Carotid Artery Thrombosis 47 4.126
9
HPT002 Hepatic Vein Thrombosis 66 4.046
10
INT076 Intracranial Sinus Thrombosis 15 3.294
11
CRB132 Cerebral Sinovenous Thrombosis 42 2.959
12
VNS011 Venous Thrombosis, Protection Against 6 2.651
13
THR062 Thrombosis, Hyperhomocysteinemic 12 2.637
14
DPV002 Deep Venous Thrombosis, Protection Against 6 2.637
15
DYS078 Dysfibrinogenemia, Alpha Type, Causing Recurrent Thrombosis 5 2.637
16
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 5 2.637
17
MND006 Mondor Disease 20 1.898
18
VNS012 Venous Thoracic Outlet Syndrome 19 1.865
19
CRB009 Cerebritis 39 0.498
20
PRT014 Protein S Deficiency 67 0.269
21
c HPT021 Hepatitis 64 0.269
22
P THR015 Thrombophilia 66 0.262
23
P MYC007 Myocardial Infarction 92 0.258
24
PLM033 Pulmonary Embolism 64 0.243
25
c THR014 Thrombocytopenia 70 0.239
26
HPR003 Heparin-Induced Thrombocytopenia 53 0.234
27
PRT011 Protein C Deficiency 55 0.232
28
ANT006 Antiphospholipid Syndrome 65 0.226
29
ANR040 Aneurysm 44 0.198
30
P HYP075 Hypertension 85 0.191
31
HPT023 Hepatocellular Carcinoma 79 0.190
32
THR079 Thromboembolism 64 0.179
33
ANT009 Antithrombin Iii Deficiency 60 0.178
34
P SYS001 Systemic Lupus Erythematosus 85 0.175
35
c LPS004 Lupus Erythematosus 72 0.175
36
HYP037 Hyperhomocysteinemia 51 0.172
37
END072 Endotheliitis 50 0.171
38
c ESS003 Essential Thrombocythemia 59 0.160
39
c NPH012 Nephrotic Syndrome 66 0.155
40
P LKM002 Leukemia 77 0.143
41
c ACT075 Acute Myocardial Infarction 59 0.142
42
c PNC044 Pancreatitis 69 0.140
43
THR016 Thrombophlebitis 68 0.138
44
c PLY018 Polycythemia 61 0.138
45
ULC004 Ulcerative Colitis 63 0.136
46
VNS010 Venous Thromboembolism 53 0.136
47
HMG002 Hemoglobinuria 52 0.136
48
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 56 0.134
49
PLY001 Polycythemia Vera 82 0.132
50
ART111 Artery Disease 60 0.129
51
HDC001 Headache 58 0.127
52
ATH003 Atherosclerosis 68 0.125
53
P PRT013 Portal Hypertension 66 0.125
54
c MYL014 Myeloproliferative Disorder 52 0.125
55
LVR012 Liver Cirrhosis 75 0.123
56
P SNS014 Sinusitis 57 0.121
57
DSS009 Disseminated Intravascular Coagulation 62 0.116
58
RTN023 Retinitis 53 0.116
59
c MNN013 Meningitis 68 0.114
60
PRP030 Purpura 64 0.112
61
THR004 Thrombocytosis 59 0.112
62
INT003 Intracranial Hypotension 30 0.110
63
CLL003 Cellulitis 58 0.107
64
P INF037 Inflammatory Bowel Disease 45 0.107
65
OTT002 Otitis Media 59 0.105
66
P DYS026 Dysfibrinogenemia 52 0.105
67
HDN002 Head Injury 48 0.103
68
CRN211 Coronary Artery Disease 84 0.100
69
OVR029 Ovarian Hyperstimulation Syndrome 66 0.098
70
ISC004 Ischemia 63 0.098
71
P HYP098 Hypereosinophilic Syndrome 61 0.098
72
c ART084 Arteriovenous Fistula 45 0.098
73
FCT004 Factor Xii Deficiency 65 0.095
74
P HMC002 Homocystinuria 58 0.095
75
PSD002 Pseudotumor Cerebri 55 0.095
76
INT075 Intracranial Hypertension 51 0.095
77
BLN003 Blindness 52 0.092
78
THR013 Thoracic Outlet Syndrome 52 0.090
79
TBR010 Tuberculosis 83 0.087
80
P OBS005 Obesity 89 0.084
81
PST095 Post-Thrombotic Syndrome 39 0.084
82
c HMP007 Hemophilia 67 0.081
83
c ACT027 Acute Pancreatitis 63 0.081
84
DFC004 Deficiency Anemia 62 0.081
85
PPL021 Papilledema 56 0.081
86
MYM001 Myoma 52 0.081
87
PRG060 Pregnancy Loss 47 0.081
88
FCT007 Factor Vii Deficiency 78 0.078
89
THR006 Thromboangiitis Obliterans 77 0.078
90
CRH001 Crohn's Disease 74 0.078
91
ACT119 Acute Promyelocytic Leukemia 66 0.078
92
CRB039 Cerebrovascular Disease 64 0.078
93
P ADN016 Adenocarcinoma 58 0.078
94
IRN001 Iron Deficiency Anemia 57 0.078
95
c OST028 Osteochondroma 54 0.078
96
CTS005 Catastrophic Antiphospholipid Syndrome 52 0.078
97
CRD137 Cardiogenic Shock 48 0.078
98
P SPR035 Superior Vena Cava Syndrome 42 0.078
99
ORB006 Orbital Cellulitis 30 0.078
100
VSC007 Vascular Disease 70 0.074
101
PTN001 Patent Foramen Ovale 61 0.074
102
P RTN022 Retinal Vein Occlusion 56 0.074
103
c LYM026 Lymphoblastic Leukemia 54 0.074
104
CYT008 Cytomegalovirus Infection 43 0.074
105
SPL006 Splenic Infarction 39 0.074
106
c DBT009 Diabetes Mellitus 78 0.071
107
BHC002 Behcet's Disease 76 0.071
108
ANK002 Ankylosing Spondylitis 74 0.071
109
P ANG001 Angelman Syndrome 70 0.071
110
ACN002 Acanthosis Nigricans 69 0.071
111
P GLM007 Glomerulonephritis 68 0.071
112
P HYD006 Hydrocephalus 68 0.071
113
STR067 Stroke, Ischemic 64 0.071
114
ART019 Aortic Valve Stenosis 64 0.071
115
c AFB001 Afibrinogenemia 60 0.071
116
P CRV039 Cervicitis 57 0.071
117
c RTN014 Retinal Artery Occlusion 57 0.071
118
c CNT016 Central Retinal Vein Occlusion 55 0.071
119
P HYP083 Hypopituitarism 52 0.071
120
MMB002 Membranous Glomerulonephritis 51 0.071
121
CRN006 Coronary Aneurysm 48 0.071
122
CRT015 Carotid Artery Occlusion 44 0.071
123
SPN185 Spinal Cord Infarction 42 0.071
124
P ATX010 Ataxia Neuropathy Spectrum 41 0.071
125
SYN053 Syndromic Diarrhea 32 0.071
126
P BRS047 Breast Cancer 100 0.067
127
P MYL005 Myelofibrosis 72 0.067
128
PRT036 Peritonitis 71 0.067
129
SPS077 Sepsis 70 0.067
130
VNW001 Von Willebrand's Disease 69 0.067
131
THY033 Thyrotoxicosis 57 0.067
132
CHY006 Chylous Ascites 48 0.067
133
THR035 Thrombasthenia 45 0.067
134
LMR001 Lemierre's Syndrome 32 0.067
135
CDS001 Cadasil 84 0.063
136
P HMP004 Hemophilia B 77 0.063
137
P ART022 Arthritis 75 0.063
138
PRC016 Pre-Eclampsia 74 0.063
139
ART016 Aortic Aneurysm 70 0.063
140
SRC014 Sarcoma 69 0.063
141
VSC011 Vasculitis 66 0.063
142
ECL001 Eclampsia 64 0.063
143
FCT006 Factor V Deficiency 63 0.063
144
c HYP076 Hyperthyroidism 62 0.063
145
P HRD011 Hereditary Spherocytosis 62 0.063
146
SND002 Sneddon Syndrome 59 0.063
147
SCK005 Sickle Cell Disease 58 0.063
148
P END033 Endocarditis 56 0.063
149
HLL004 Hellp Syndrome 54 0.063
150
P CNT028 Central Retinal Artery Occlusion 52 0.063
151
PRP034 Purpura Fulminans 52 0.063
152
NNT024 Neonatal Stroke 50 0.063
153
HMC014 Homocysteinemia 48 0.063
154
EVN001 Evans' Syndrome 46 0.063
155
ANG054 Angina Pectoris 46 0.063
156
BRS090 Breast Reconstruction 44 0.063
157
BRN026 Branch Retinal Artery Occlusion 43 0.063
158
VRC005 Varicose Veins 42 0.063
159
FCT013 Factor V Leiden Thrombophilia 33 0.063
160
P ATX002 Ataxia Telangiectasia 86 0.059
161
P APL001 Aplastic Anemia 82 0.059
162
MYL040 Myelodysplastic Syndromes 79 0.059
163
KWS002 Kawasaki Disease 73 0.059
164
c THL005 Thalassemia 72 0.059
165
P LVR013 Liver Disease 69 0.059
166
ART021 Arteriosclerosis 67 0.059
167
P HPT001 Hepatitis C 66 0.059
168
LGG001 Legg-Calve-Perthes Disease 65 0.059
169
FCT002 Factor Xi Deficiency 64 0.059
170
P RNL014 Renal Cell Carcinoma 62 0.059
171
ART005 Arteriovenous Malformation 62 0.059
172
NRP001 Neuropathy 61 0.059
173
CHL067 Cholecystitis 60 0.059
174
ANT058 Anterior Ischemic Optic Neuropathy 59 0.059
175
P CNG019 Congenital Afibrinogenemia 58 0.059
176
P INT030 Intracranial Aneurysm 57 0.059
177
ART001 Arterial Tortuosity Syndrome 54 0.059
178
AND003 Andersen-Tawil Syndrome 53 0.059
179
P THR090 Thrombocythemia 1 52 0.059
180
BRN106 Burns 49 0.059
181
MNN021 Meningococcemia 48 0.059
182
P VNS003 Venous Insufficiency 46 0.059
183
CHR466 Chronic Thromboembolic Pulmonary Hypertension 43 0.059
184
SPP008 Suppurative Otitis Media 41 0.059
185
P CRN074 Coronary Artery Aneurysm 40 0.059
186
PRP028 Peripheral Vertigo 40 0.059
187
c ACQ012 Acquired Angioedema 38 0.059
188
PTR001 Petrositis 29 0.059
189
P LPR003 Leprosy 77 0.055
190
P PNM007 Pneumonia 76 0.055
191
GLN003 Glanzmann's Thrombasthenia 73 0.055
192
c MYL006 Myeloid Leukemia 72 0.055
193
ASP006 Aspergillosis 72 0.055
194
c HYP095 Hypercholesterolemia 70 0.055
195
c HPT016 Hepatitis B 68 0.055
196
P ABD003 Abdominal Aortic Aneurysm 67 0.055
197
DBT001 Diabetic Ketoacidosis 65 0.055
198
FCT003 Factor X Deficiency 63 0.055
199
SPN186 Spinal Cord Injury 63 0.055
200
BLR001 Biliary Atresia 62 0.055
201
SPT013 Septic Shock 60 0.055
202
PRP007 Priapism 60 0.055
203
SPH001 Sapho Syndrome 59 0.055
204
c THR005 Thrombotic Thrombocytopenic Purpura 58 0.055
205
HYP063 Hypersplenism 58 0.055
206
c ACT073 Acute Leukemia 56 0.055
207
P CMP008 Compartment Syndrome 56 0.055
208
c ACR001 Aicardi-Goutieres Syndrome 53 0.055
209
c ACQ014 Acquired Hemophilia 52 0.055
210
MNT147 Mental Retardation 51 0.055
211
PRT019 Protein-Losing Enteropathy 50 0.055
212
MLK003 Melkersson-Rosenthal Syndrome 50 0.055
213
TYP013 Type 1 Von Willebrand Disease 50 0.055
214
ERY004 Erysipelas 50 0.055
215
FCT005 Factor Xiii Deficiency 49 0.055
216
ACT099 Acute Fatty Liver of Pregnancy 49 0.055
217
ABD004 Abdominal Tuberculosis 46 0.055
218
MDS022 Mediastinitis 46 0.055
219
BLD054 Blood Protein Disease 36 0.055
220
INF133 Inferior Vena Cava Interruption 35 0.055
221
HMC004 Homocysteine Plasma Level 33 0.055
222
MTH044 Mthfr Gene Mutation 32 0.055
223
c FRN011 Frontal Sinusitis 30 0.055
224
SBD001 Subdural Empyema 28 0.055
225
PRX023 Paroxysmal Nocturnal Hemoglobinuria, Somatic 26 0.055
226
SPH007 Sphenoid Sinusitis 26 0.055
227
c BNG076 Benign Exophthalmos Syndrome 22 0.055
228
HGH021 Hughes-Stovin Syndrome 21 0.055
229
HDG007 Hodgkin's Lymphoma 92 0.050
230
AND002 Androgen Insensitivity Syndrome 80 0.050
231
P PHC003 Pheochromocytoma 78 0.050
232
P CLN016 Colon Cancer 78 0.050
233
BRK003 Burkitt's Lymphoma 77 0.050
234
P FML018 Familial Mediterranean Fever 74 0.050
235
P LNG032 Lung Cancer 72 0.050
236
SCK003 Sickle Cell Anemia 72 0.050
237
P TMP003 Temporal Arteritis 71 0.050
238
RLP001 Relapsing Polychondritis 70 0.050
239
FCT001 Factor Viii Deficiency 70 0.050
240
GST009 Gastroschisis 66 0.050
241
c AXN002 Axenfeld-Rieger Syndrome 66 0.050
242
P BRN019 Bernard-Soulier Syndrome 64 0.050
243
P LMY004 Leiomyosarcoma 64 0.050
244
c INT070 Intestinal Obstruction 63 0.050
245
P ESN007 Eosinophilia 61 0.050
246
c MYL007 Myeloma 61 0.050
247
ACQ007 Acquired Immunodeficiency Syndrome 61 0.050
248
PRS047 Prostatitis 60 0.050
249
P CNG401 Congenital Heart Disease 58 0.050
250
MYC002 Mycobacterium Avium Complex Disease 58 0.050
251
OST017 Osteomyelitis 58 0.050
252
ANR004 Anuria 57 0.050
253
CHR001 Churg-Strauss Syndrome 57 0.050
254
NDL013 Nodular Regenerative Hyperplasia 56 0.050
255
DDN006 Duodenitis 56 0.050
256
APP008 Appendicitis 55 0.050
257
HPT019 Hepatic Encephalopathy 55 0.050
258
RDC002 Radiculopathy 55 0.050
259
NPH051 Nephritis 54 0.050
260
CHL069 Cholesteatoma 54 0.050
261
MYL001 Myelitis 54 0.050
262
P PYL005 Pyelonephritis 54 0.050
263
KLN001 Klinefelter's Syndrome 52 0.050
264
EXS001 Exostosis 51 0.050
265
CCN002 Cocaine Abuse 50 0.050
266
c SVR056 Severe Hemophilia a 49 0.050
267
NNR007 Non-Arteritic Anterior Ischemic Optic Neuropathy 48 0.050
268
RTR011 Retroperitoneal Fibrosis 48 0.050
269
BCT015 Bacteremia 48 0.050
270
ZYG002 Zygomycosis 44 0.050
271
VND001 Vein Disease 44 0.050
272
ART110 Arteritic Anterior Ischemic Optic Neuropathy 43 0.050
273
CDQ001 Cauda Equina Syndrome 43 0.050
274
AMR003 Amaurosis Fugax 40 0.050
275
LCK001 Locked-in Syndrome 40 0.050
276
PRP080 Peripheral Artery Disease 34 0.050
277
CRT012 Cortical Blindness 34 0.050
278
AND005 Androgen Insensitivity Syndrome, Mild 21 0.050
279
HRD083 Hereditary Antithrombin Deficiency 20 0.050
280
c THR023 Thrombophilia Due to Thrombomodulin Defect 9 0.050
281
P ACT019 Acute Myeloid Leukemia 92 0.045
282
P FML021 Familial Hypercholesterolemia 85 0.045
283
c BTT002 Beta Thalassemia 77 0.045
284
P ACT074 Acute Lymphocytic Leukemia 75 0.045
285
TTR001 Tetralogy of Fallot 74 0.045
286
P WGN002 Wegener's Granulomatosis 71 0.045
287
P MLT020 Multiple Sclerosis 69 0.045
288
P HML002 Hemolytic Anemia 66 0.045
289
MRB003 Morbid Obesity 66 0.045
290
c THY032 Thyroiditis 66 0.045
291
P GRV001 Graves' Disease 64 0.045
292
CRN036 Craniopharyngioma 63 0.045
293
P SCH018 Schizencephaly 61 0.045
294
TYP007 Typhoid Fever 60 0.045
295
ADR015 Adrenocortical Carcinoma 60 0.045
296
c HMR012 Hemorrhagic Fever 60 0.045
297
CHR074 Choriocarcinoma 59 0.045
298
P END047 Endophthalmitis 59 0.045
299
c SLP006 Sleep Apnea 59 0.045
300
PNM013 Pneumococcal Meningitis 55 0.045
301
CRD001 Cardiac Tamponade 55 0.045
302
INT002 Intermittent Claudication 55 0.045
303
ANG011 Angiodysplasia 54 0.045
304
INT007 Intermediate Coronary Syndrome 54 0.045
305
c ACT134 Acute Liver Failure 53 0.045
306
SPT004 Septic Arthritis 53 0.045
307
LPS007 Lupus Nephritis 52 0.045
308
ANG018 Angiomyolipoma 51 0.045
309
HMR002 Hemarthrosis 51 0.045
310
CRN020 Coronary Restenosis 50 0.045
311
c ERY013 Erythrocytosis 50 0.045
312
OPT009 Optic Neuritis 49 0.045
313
P PND001 Pain Disorder 48 0.045
314
SPN035 Spindle Cell Sarcoma 48 0.045
315
NRT004 Neuritis 48 0.045
316
CHL004 Cholelithiasis 47 0.045
317
c PRN026 Porencephaly 47 0.045
318
ACQ017 Acquired Von Willebrand Syndrome 47 0.045
319
LYM021 Lymphadenitis 47 0.045
320
ESN011 Eisenmenger Syndrome 46 0.045
321
VTM002 Vitamin B12 Deficiency 46 0.045
322
NRN002 Neuronitis 43 0.045
323
NPH017 Nephrosis 42 0.045
324
CRB086 Cerebral Aneurysms 38 0.045
325
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 37 0.045
326
SCR015 Scarlet Fever 37 0.045
327
c CHR431 Chronic Venous Insufficiency 37 0.045
328
MYC020 Mycobacterium Tuberculosis, Susceptibility to Infection by 37 0.045
329
HMR001 Hemorrhagic Thrombocythemia 33 0.045
330
VNF001 Vein of Galen Aneurysm 30 0.045
331
CNG058 Congenital Antithrombin Deficiency Type 3 28 0.045
332
IRN002 Iron Metabolism Disease 26 0.045
333
SHW001 Shwartzman Phenomenon 25 0.045
334
HMC030 Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency 19 0.045
335
THN005 Thunderclap Headache 19 0.045
336
DBL009 Double Inferior Vena Cava 18 0.045
337
ORB016 Orbital Varix 14 0.045
338
MYT019 May–thurner Syndrome 12 0.045
339
P RHM011 Rheumatoid Arthritis 93 0.039
340
P MLT019 Multiple Myeloma 82 0.039
341
P PRM021 Primary Pulmonary Hypertension 82 0.039
342
P OVR042 Ovarian Cancer 81 0.039
343
P CLC005 Celiac Disease 74 0.039
344
P AST007 Astrocytoma 71 0.039
345
c CHR065 Chronic Myeloid Leukemia 71 0.039
346
SCH014 Schistosomiasis 70 0.039
347
DRM006 Dermatitis 69 0.039
348
c CHR090 Chronic Lymphocytic Leukemia 67 0.039
349
GSG001 Gas Gangrene 67 0.039
350
PRP027 Peripheral Vascular Disease 67 0.039
351
P TRN020 Turner Syndrome 66 0.039
352
c ENC004 Encephalitis 65 0.039
353
PHR003 Pharyngitis 65 0.039
354
c VRL010 Viral Hepatitis 64 0.039
355
P CNJ013 Conjunctivitis 63 0.039
356
c MLG069 Malignant Hypertension 63 0.039
357
P MLN008 Melanoma 63 0.039
358
P ESP024 Esophagitis 63 0.039
359
HYP066 Hyperglycemia 62 0.039
360
c KDN018 Kidney Disease 62 0.039
361
P MTR012 Mitral Valve Disease 62 0.039
362
HYD012 Hydrops Fetalis 61 0.039
363
P RNV001 Renovascular Hypertension 61 0.039
364
P LPS002 Liposarcoma 61 0.039
365
c ATM010 Autoimmune Hemolytic Anemia 60 0.039
366
CHC001 Chickenpox 60 0.039
367
c ALM001 Al Amyloidosis 59 0.039
368
MGC001 Megacolon 59 0.039
369
PRT039 Proteinuria 57 0.039
370
BRN029 Brain Disease 57 0.039
371
BRN071 Brain Injury 57 0.039
372
URM002 Uremia 56 0.039
373
P MYM002 Moyamoya Disease 56 0.039
374
HST009 Histiocytoma 55 0.039
375
P EXP004 Exophthalmos 54 0.039
376
NPH011 Nephroblastoma 54 0.039
377
LYM019 Lymphosarcoma 54 0.039
378
c LYM025 Lymphedema 53 0.039
379
TRM010 Traumatic Brain Injury 53 0.039
380
c OPH004 Ophthalmoplegia 53 0.039
381
PRC013 Pericarditis 53 0.039
382
LPD004 Lipoid Nephrosis 51 0.039
383
MNN014 Mononeuritis 51 0.039
384
VRC001 Varicocele 50 0.039
385
P CHR092 Chronic Myeloproliferative Disease 50 0.039
386
TRN007 Transsexualism 49 0.039
387
P PNC001 Pancytopenia 48 0.039
388
PRP016 Paraplegia 47 0.039
389
RTN021 Retinal Vascular Occlusion 47 0.039
390
SVR005 Severe Pre-Eclampsia 47 0.039
391
ACT055 Actinomycosis 46 0.039
392
END021 Endomyocardial Fibrosis 46 0.039
393
P HMG003 Hemoglobin E Disease 45 0.039
394
PRT093 Proteus Syndrome, Somatic 45 0.039
395
c HPT073 Hepatitis C Virus 45 0.039
396
FSC004 Fasciitis 45 0.039
397
CRP018 Cor Pulmonale 44 0.039
398
LMB062 Limb Ischemia 44 0.039
399
OBS004 Obstructive Hydrocephalus 43 0.039
400
c ACT042 Acute Pyelonephritis 42 0.039
401
PLS018 Plasminogen Activator Inhibitor Type 1 Deficiency 42 0.039
402
EPD005 Epidural Abscess 42 0.039
403
HNC001 Henoch-Schoenlein Purpura 41 0.039
404
CNT060 Central Serous Chorioretinopathy 41 0.039
405
TYP015 Type 2b Von Willebrand Disease 40 0.039
406
INF013 Inferior Myocardial Infarction 40 0.039
407
BNM005 Bone Marrow Necrosis 39 0.039
408
TRC023 Trichinosis 38 0.039
409
BCK006 Back Pain 38 0.039
410
STR044 Steroid-Resistant Nephrotic Syndrome 37 0.039
411
PRS045 Prostatic Hypertrophy 37 0.039
412
HNS001 Hansen's Disease 36 0.039
413
P LBY004 Labyrinthitis 34 0.039
414
LYM014 Lymphangitis 33 0.039
415
HMC020 Homocystinuria, B6-Responsive and Nonresponsive Types 33 0.039
416
c CRN035 Cranial Nerve Palsy 31 0.039
417
P INF069 Infantile Neuroaxonal Dystrophy 1 31 0.039
418
P ATM020 Autoimmune Enteropathy 30 0.039
419
TYP018 Type 3 Von Willebrand Disease 30 0.039
420
ALX001 Alexia 30 0.039
421
TXC001 Toxic Megacolon 29 0.039
422
PRT045 Prothrombin-Related Thrombophilia 28 0.039
423
BSL004 Basilar Artery Occlusion 28 0.039
424
PSL001 Pasli Disease 27 0.039
425
ETH009 Ethmoid Sinusitis 26 0.039
426
THR089 Thrombophilia Due to Protein S Deficiency, Autosomal Dominant 25 0.039
427
PL2001 Pla2g6-Associated Neurodegeneration 24 0.039
428
ART007 Aorta Atresia 22 0.039
429
THR007 Thrombophlebitis Migrans 21 0.039
430
ABD009 Abducens Palsy 18 0.039
431
PRN017 Perianal Hematoma 15 0.039
432
CNG056 Congenital Antithrombin Deficiency 12 0.039
433
P ALZ001 Alzheimer's Disease 97 0.032
434
CYS001 Cystic Fibrosis 96 0.032
435
P TYP008 Type 1 Diabetes Mellitus 93 0.032
436
P PNC035 Pancreatic Cancer 91 0.032
437
P LFR001 Li-Fraumeni Syndrome 87 0.032
438
P TBR001 Tuberous Sclerosis 85 0.032
439
P FML011 Familial Adenomatous Polyposis 85 0.032
440
GLC006 Galactosemia 81 0.032
441
P MNN012 Meningioma 78 0.032
442
P MDL005 Medulloblastoma 77 0.032
443
P NRL016 Neural Tube Defects 77 0.032
444
P CLR023 Colorectal Cancer 73 0.032
445
c PRM002 Primary Hyperoxaluria 72 0.032
446
OBS002 Obsessive-Compulsive Disorder 72 0.032
447
P PRD006 Prader-Willi Syndrome 71 0.032
448
c MST009 Mastocytosis 71 0.032
449
P NRB001 Neuroblastoma 70 0.032
450
CCC001 Coccidioidomycosis 70 0.032
451
P HMN010 Hemangioma 70 0.032
452
GLL008 Gilles De La Tourette Syndrome 70 0.032
453
P END044 Endometriosis 69 0.032
454
P MGR002 Migraine 69 0.032
455
CHL065 Cholangiocarcinoma 69 0.032
456
TKY001 Takayasu's Arteritis 69 0.032
457
c HYP086 Hypothyroidism 69 0.032
458
P KDN017 Kidney Cancer 68 0.032
459
ATM004 Autoimmune Thrombocytopenic Purpura 68 0.032
460
SCR008 Scrub Typhus 68 0.032
461
CRY005 Cryptococcosis 68 0.032
462
KLP002 Klippel-Trenaunay Syndrome 67 0.032
463
P PLY011 Polycystic Ovary Syndrome 66 0.032
464
P SYS004 Systemic Mastocytosis 66 0.032
465
NNH001 Non-Hodgkin Lymphoma 66 0.032
466
P GST044 Gastritis 66 0.032
467
P PRD008 Periodontitis 66 0.032
468
P ANR007 Anorexia Nervosa 66 0.032
469
P INS005 Insulin Resistance 66 0.032
470
OLL001 Ollier Disease 66 0.032
471
STT001 Status Epilepticus 65 0.032
472
CRB037 Cerebral Palsy 65 0.032
473
P DYS007 Dyskeratosis Congenita 65 0.032
474
MLG056 Malignant Hyperthermia 64 0.032
475
P HRD057 Hereditary Pancreatitis 64 0.032
476
ADN018 Adenoma 64 0.032
477
DBN001 Dubin-Johnson Syndrome 64 0.032
478
P OLG002 Oligodendroglioma 64 0.032
479
PMS001 Poems Syndrome 63 0.032
480
c EHL001 Ehlers-Danlos Syndrome 63 0.032
481
P CMP010 Complex Regional Pain Syndrome 63 0.032
482
c HYP061 Hypertrophic Cardiomyopathy 63 0.032
483
HYP056 Hypoglycemia 63 0.032
484
CYS005 Cysticercosis 63 0.032
485
c MSC005 Muscular Dystrophy 62 0.032
486
P ANP001 Anaplastic Large Cell Lymphoma 62 0.032
487
VGN023 Vaginitis 62 0.032
488
ART031 Aortic Coarctation 62 0.032
489
GNG013 Gingivitis 62 0.032
490
P RBL001 Rubella 62 0.032
491
ADL030 Adult-Onset Still's Disease 61 0.032
492
P CRB042 Cerebellar Ataxia 61 0.032
493
MYL020 Myelomeningocele 61 0.032
494
P ERY008 Erythromelalgia 61 0.032
495
TXC005 Toxic Shock Syndrome 61 0.032
496
DWN001 Down Syndrome 61 0.032
497
ASP003 Aseptic Meningitis 60 0.032
498
PLM001 Pulmonary Tuberculosis 60 0.032
499
P MLG002 Malignant Peritoneal Mesothelioma 60 0.032
500
P SYR001 Syringomyelia 60 0.032
501
P CRV035 Cervical Cancer 60 0.032
502
P HYP080 Hypogonadism 59 0.032
503
GLB015 Glioblastoma Multiforme 59 0.032
504
c HPT003 Hepatitis a 59 0.032
505
CVR006 Cavernous Hemangioma 58 0.032
506
CNN005 Connective Tissue Disease 58 0.032
507
c ATX004 Ataxia 58 0.032
508
PRC012 Pericardial Effusion 58 0.032
509
P PLC011 Pilocytic Astrocytoma 57 0.032
510
CRY004 Cryoglobulinemia 57 0.032
511
P DBT005 Diabetes Insipidus 57 0.032
512
RHB003 Rhabdomyosarcoma 57 0.032
513
P MYC008 Myocarditis 57 0.032
514
HYP266 Hypoxia 57 0.032
515
c HPT015 Hepatitis D 57 0.032
516
TNS005 Tonsillitis 57 0.032
517
c ANG015 Angioedema 57 0.032
518
c CTR002 Cataract 57 0.032
519
ACT017 Acute Chest Syndrome 56 0.032
520
P MLG077 Malignant Peripheral Nerve Sheath Tumor 56 0.032
521
PYD001 Pyoderma Gangrenosum 55 0.032
522
TYP011 Typhus 55 0.032
523
MCR088 Microscopic Polyangiitis 55 0.032
524
CCT002 Cicatricial Pemphigoid 55 0.032
525
P CHL066 Cholangitis 54 0.032
526
P HMN013 Hemangiopericytoma 54 0.032
527
LYM040 Lymphoblastic Lymphoma 54 0.032
528
ORL011 Oral Cancer 53 0.032
529
END031 Endometrial Stromal Sarcoma 53 0.032
530
INT221 Intravascular Large B-Cell Lymphoma 53 0.032
531
BRN004 Brain Edema 53 0.032
532
STS002 Situs Inversus 53 0.032
533
c HYD002 Hydronephrosis 53 0.032
534
PRN011 Pernicious Anemia 53 0.032
535
HMP005 Hemiplegia 52 0.032
536
P ENC008 Encephalocele 52 0.032
537
ATP002 Atopy 52 0.032
538
CRV031 Cervical Adenocarcinoma 52 0.032
539
TRN015 Transient Cerebral Ischemia 52 0.032
540
ALC009 Alcoholic Liver Cirrhosis 51 0.032
541
PYD002 Pyoderma 51 0.032
542
HPT032 Hepatocellular Carcinoma, Somatic 51 0.032
543
PLV003 Pelvic Inflammatory Disease 51 0.032
544
OBS001 Obstructive Jaundice 50 0.032
545
ARR001 Arrhythmogenic Right Ventricular Dysplasia 50 0.032
546
CRN014 Cronkhite-Canada Syndrome 50 0.032
547
PLC007 Placental Abruption 50 0.032
548
CYS009 Cystadenoma 50 0.032
549
CLS010 Cluster Headache 50 0.032
550
SCT005 Scott Syndrome 50 0.032
551
c BCT007 Bacterial Meningitis 49 0.032
552
SYN006 Synovial Sarcoma 49 0.032
553
c PSD003 Pseudohypoaldosteronism 49 0.032
554
SMN007 Seminoma 49 0.032
555
P BCL006 B-Cell Lymphomas 49 0.032
556
P GRM009 Germ Cell Tumors 49 0.032
557
RFL001 Reflex Sympathetic Dystrophy 48 0.032
558
MTS001 Mutism 48 0.032
559
P BLD034 Bile Duct Carcinoma 48 0.032
560
PNV001 Panuveitis 48 0.032
561
PYM001 Pyomyositis 47 0.032
562
URT010 Ureteral Obstruction 47 0.032
563
PNN001 Panniculitis 46 0.032
564
HPT008 Hepatic Tuberculosis 46 0.032
565
P WRF002 Warfarin Sensitivity 46 0.032
566
P HMR005 Hemorrhoid 46 0.032
567
P ATR005 Atrophic Gastritis 46 0.032
568
HMN016 Hemangioendothelioma 45 0.032
569
PNH001 Panhypopituitarism 45 0.032
570
P CRT018 Carotid Intimal Medial Thickness 45 0.032
571
PLR007 Pleural Empyema 45 0.032
572
FRM007 Freeman Sheldon Syndrome 45 0.032
573
SFT003 Soft Tissue Sarcoma 45 0.032
574
ILS001 Ileus 44 0.032
575
SYS011 Systemic Lupus Erythematosus, Association with 44 0.032
576
CLL002 Collecting Duct Carcinoma 44 0.032
577
TRN012 Transient Global Amnesia 43 0.032
578
QDR001 Quadriplegia 43 0.032
579
LNG029 Lung Adenocarcinoma 42 0.032
580
P HRN001 Horner's Syndrome 42 0.032
581
ENC017 Encephaloceles 42 0.032
582
CGN002 Cogan's Syndrome 41 0.032
583
HYP265 Hypotonia 41 0.032
584
FCL012 Facial Paralysis 40 0.032
585
c PRT096 Peritoneal Mesothelioma 40 0.032
586
P APL006 Aplasia Cutis Congenita 40 0.032
587
LMY003 Leiomyomatosis 39 0.032
588
INT079 Intrahepatic Cholangiocarcinoma 39 0.032
589
FNT004 Fainting 38 0.032
590
MYS004 Myiasis 38 0.032
591
c SPH018 Spherocytosis, Hereditary, Type 5 38 0.032
592
PRS021 Prostatic Adenoma 38 0.032
593
ANG017 Angiolipoma 36 0.032
594
ESN020 Eosinophilic Granulomatosis with Polyangiitis 36 0.032
595
RHM028 Rheumatic Heart Disease 36 0.032
596
VRL011 Viral Infectious Disease 36 0.032
597
c SBC003 Subacute Bacterial Endocarditis 35 0.032
598
MLK004 Malakoplakia 35 0.032
599
ADS002 Adie Syndrome 35 0.032
600
P MLD013 Mild Hemophilia a 35 0.032
601
LYM005 Lymphocele 33 0.032
602
P PRX010 Paroxysmal Ventricular Fibrillation 33 0.032
603
HPT066 Hepatoportal Sclerosis 32 0.032
604
HYP319 Hypereosinophilic Syndrome, Idiopathic, Resistant to Imatinib 32 0.032
605
TYP017 Type 2n Von Willebrand Disease 30 0.032
606
PNS012 Paine Syndrome 30 0.032
607
TYP014 Type 2a Von Willebrand Disease 29 0.032
608
TYP016 Type 2m Von Willebrand Disease 29 0.032
609
NRR001 Neuroretinitis 29 0.032
610
FBR028 Fibrosing Mediastinitis 29 0.032
611
PRR008 Periarteritis Nodosa 28 0.032
612
TFT003 Tufting Enteropathy 28 0.032
613
WND002 Wandering Spleen 28 0.032
614
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.032
615
HPT012 Hepatocellular Fibrolamellar Carcinoma 27 0.032
616
HNM002 Hinman Syndrome 27 0.032
617
PRM008 Parametritis 27 0.032
618
CHR158 Charles Bonnet Syndrome 26 0.032
619
STR077 Streptococcal Toxic-Shock Syndrome 26 0.032
620
c ACT036 Acute Cholangitis 25 0.032
621
P HYP078 Hypertrophy of Breast 25 0.032
622
THR067 Thrombophilia Due to Protein C Deficiency, Autosomal Dominant 24 0.032
623
P MLT009 Multiple Cranial Nerve Palsy 22 0.032
624
PRF003 Piriformis Syndrome 22 0.032
625
MSN003 Mesenteric Vascular Occlusion 22 0.032
626
c ACT035 Acute Frontal Sinusitis 21 0.032
627
HMC016 Homocystinuria Due to Cbs Deficiency 20 0.032
628
SCT001 Sciatic Neuropathy 20 0.032
629
MNN005 Meningovascular Neurosyphilis 19 0.032
630
c ACT061 Acute Sphenoidal Sinusitis 17 0.032
631
PLM062 Pulmonary Hyalinizing Granuloma 14 0.032
632
OCL024 Ocular Neuromyotonia 14 0.032
633
MCR033 Macrocephaly-Capillary Malformation 14 0.032
634
CGH002 Cough Headache 14 0.032
635
SNG003 Single Ventricular Heart 14 0.032
636
CRT056 Carotidynia 13 0.032
637
MTH028 Mthfr Thermolabile Variant 11 0.032
638
NNT044 Neonatal Antiphospholipid Syndrome 10 0.032
639
THR088 Thrombophilia Due to Protein S Deficiency, Autosomal Recessive 8 0.032
640
ACT174 Acute Peripheral Arterial Occlusion 8 0.032
641
c TYP009 Type 2 Diabetes Mellitus 95 0.022
642
P PRK002 Parkinson's Disease 92 0.022
643
P DLT002 Dilated Cardiomyopathy 82 0.022
644
P RTT002 Rett Syndrome 82 0.022
645
FBR012 Fabry Disease 81 0.022
646
P HRD008 Hereditary Hemorrhagic Telangiectasia 81 0.022
647
SVR004 Severe Combined Immunodeficiency 80 0.022
648
P HMC003 Hemochromatosis 78 0.022
649
P WSK001 Wiskott-Aldrich Syndrome 78 0.022
650
CNG034 Congestive Heart Failure 78 0.022
651
ACT033 Acute Intermittent Porphyria 76 0.022
652
PTZ001 Peutz-Jeghers Syndrome 76 0.022
653
CRB011 Cerebrotendinous Xanthomatosis 75 0.022
654
P RBN001 Rubinstein-Taybi Syndrome 75 0.022
655
P MLR004 Malaria 75 0.022
656
DCH001 Duchenne Muscular Dystrophy 74 0.022
657
c NNN003 Noonan Syndrome 73 0.022
658
THY028 Thyroid Cancer 73 0.022
659
P LYM007 Lymphangioleiomyomatosis 73 0.022
660
P FRG001 Fragile X Syndrome 73 0.022
661
c OST005 Osteogenesis Imperfecta 72 0.022
662
P PRM006 Primary Biliary Cirrhosis 72 0.022
663
PLY017 Polyarteritis Nodosa 69 0.022
664
BLL006 Bullous Pemphigoid 69 0.022
665
P RTH001 Rothmund-Thomson Syndrome 68 0.022
666
c SRC013 Sarcoidosis 68 0.022
667
LKC001 Leukocyte Adhesion Deficiency 68 0.022
668
DNY001 Denys-Drash Syndrome 68 0.022
669
P INF038 Influenza 68 0.022
670
LMY002 Leiomyoma 67 0.022
671
P AMY004 Amyloidosis 67 0.022
672
ACT010 Acth-Secreting Pituitary Adenoma 67 0.022
673
SPN038 Spina Bifida 67 0.022
674
MYS005 Myositis 66 0.022
675
P ATM003 Autoimmune Thyroiditis 65 0.022
676
P HYP117 Hypertriglyceridemia 65 0.022
677
c SPN046 Spinal Muscular Atrophy 65 0.022
678
c UVT001 Uveitis 65 0.022
679
MLB002 Male Breast Cancer 65 0.022
680
P CHR089 Chronic Kidney Failure 65 0.022
681
c SCL016 Scleroderma 64 0.022
682
P ALP009 Alopecia Areata 64 0.022
683
P ATP001 Atopic Dermatitis 64 0.022
684
ARG002 Argininosuccinic Aciduria 64 0.022
685
P CNG042 Congenital Central Hypoventilation Syndrome 64 0.022
686
ARS001 Aarskog-Scott Syndrome 63 0.022
687
MXD005 Mixed Connective Tissue Disease 63 0.022
688
P CHN012 Chondrosarcoma 63 0.022
689
P ADL010 Adult Respiratory Distress Syndrome 63 0.022
690
ACT049 Acute Disseminated Encephalomyelitis 63 0.022
691
P ART023 Arthropathy 63 0.022
692
CMP002 Campylobacteriosis 63 0.022
693
P STM004 Stomach Cancer 63 0.022
694
PSR002 Psoriasis 63 0.022
695
BRN028 Brain Cancer 62 0.022
696
HPT022 Hepatoblastoma 62 0.022
697
P GTR002 Goiter 62 0.022
698
STS003 Sitosterolemia 62 0.022
699
c PRP029 Porphyria 61 0.022
700
KRN002 Kearns-Sayre Syndrome 61 0.022
701
MLD001 Melioidosis 61 0.022
702
BBS001 Babesiosis 61 0.022
703
HV1006 Hiv-1 61 0.022
704
c PLY014 Polycystic Kidney Disease 61 0.022
705
BCK001 Becker Muscular Dystrophy 61 0.022
706
BLL003 Bell's Palsy 60 0.022
707
SRS001 Serous Cystadenocarcinoma 60 0.022
708
GRY002 Gray Platelet Syndrome 60 0.022
709
P ACT009 Acute Monocytic Leukemia 60 0.022
710
BRC012 Brucellosis 60 0.022
711
P GLC007 Glaucoma 60 0.022
712
c OST026 Osteogenesis Imperfecta Type I 60 0.022
713
CHL068 Cholestasis 60 0.022
714
P PRM124 Primary Hyperoxaluria Type 1 60 0.022
715
P BRN009 Burning Mouth Syndrome 59 0.022
716
ACR008 Acrocallosal Syndrome 59 0.022
717
JCB001 Jacobsen Syndrome 59 0.022
718
RTN025 Retinoschisis 59 0.022
719
CRB021 Cerebral Malaria 59 0.022
720
CHL014 Cholera 59 0.022
721
c DMN001 Diamond-Blackfan Anemia 59 0.022
722
MLL005 Miller-Dieker Syndrome 59 0.022
723
DNG003 Dengue Disease 59 0.022
724
MCS003 Mucous Membrane Pemphigoid 58 0.022
725
BLM002 Bulimia Nervosa 58 0.022
726
MYX005 Myxoid Liposarcoma 58 0.022
727
P HRD012 Hereditary Elliptocytosis 58 0.022
728
P ALP006 Alpha Thalassemia 58 0.022
729
c MNC007 Monocytic Leukemia 58 0.022
730
PLY041 Polymyositis 58 0.022
731
NRN004 Neuroendocrine Tumor 58 0.022
732
NRN001 Neuroendocrine Carcinoma 58 0.022
733
LGN001 Legionnaires' Disease 58 0.022
734
EPT020 Epithelioid Hemangioendothelioma 58 0.022
735
DST005 Diastrophic Dysplasia 58 0.022
736
ANN002 Anencephaly 58 0.022
737
c CNG015 Congenital Diaphragmatic Hernia 58 0.022
738
NTH001 Netherton Syndrome 58 0.022
739
GLC003 Glucose Intolerance 58 0.022
740
AMN001 Amenorrhea 57 0.022
741
P SYP003 Syphilis 57 0.022
742
ADN011 Adenoid Cystic Carcinoma 57 0.022
743
ECH003 Echinococcosis 57 0.022
744
NRL005 Neurilemmoma 57 0.022
745
MCN007 Meconium Aspiration Syndrome 57 0.022
746
P RNL007 Renal Tubular Acidosis 57 0.022
747
NTR003 Natural Killer Cell Leukemia 57 0.022
748
PLS011 Plasmacytoma 57 0.022
749
P DND001 Dandy-Walker Syndrome 57 0.022
750
c THR003 Thoracic Aortic Aneurysm 57 0.022
751
ANK001 Ankylosis 57 0.022
752
HYP003 Hypermethioninemia 56 0.022
753
SDR002 Siderosis 56 0.022
754
ACT095 Acute Biphenotypic Leukemia 56 0.022
755
c HRD002 Hereditary Angioedema 56 0.022
756
P PLY006 Polydactyly 56 0.022
757
c PST005 Posterior Uveitis 56 0.022
758
CRT002 Cartilage-Hair Hypoplasia 56 0.022
759
DNG001 Dengue Shock Syndrome 56 0.022
760
CNG048 Congenital Hepatic Fibrosis 56 0.022
761
ART017 Aortic Disease 56 0.022
762
c FML035 Familial Hyperlipidemia 55 0.022
763
DBT008 Diabetic Angiopathy 55 0.022
764
LFT009 Left Ventricular Outflow Tract Obstruction 55 0.022
765
CLC001 Calciphylaxis 55 0.022
766
IMP005 Impotence 55 0.022
767
c TRT010 Teratoma 55 0.022
768
JPN002 Japanese Encephalitis 55 0.022
769
MTN003 Motion Sickness 54 0.022
770
FBR003 Fibrous Histiocytoma 54 0.022
771
EBS001 Ebstein Anomaly 54 0.022
772
GST037 Gastroparesis 54 0.022
773
CYS014 Cystadenocarcinoma 54 0.022
774
c VNT002 Ventricular Septal Defect 54 0.022
775
MCN001 Mucinous Adenocarcinoma 54 0.022
776
c ADL052 Adult Acute Lymphocytic Leukemia 54 0.022
777
GST050 Gastrointestinal System Disease 54 0.022
778
BRK001 Brooke-Spiegler Syndrome 54 0.022
779
STT004 Steatorrhea 54 0.022
780
c HRM001 Hermansky-Pudlak Syndrome 53 0.022
781
NPH010 Nephrosclerosis 53 0.022
782
P MSC003 Muscular Atrophy 53 0.022
783
END020 Endocardial Fibroelastosis 53 0.022
784
HNT002 Hantavirus Pulmonary Syndrome 53 0.022
785
SPR004 Supravalvular Aortic Stenosis 53 0.022
786
KLT001 Klatskin's Tumor 53 0.022
787
OBS061 Obstructive Sleep Apnea 52 0.022
788
P DYS142 Dyskeratosis Congenita, Autosomal Recessive 4 52 0.022
789
INV001 Invasive Aspergillosis 52 0.022
790
STN007 Stenotrophomonas Maltophilia 52 0.022
791
c RST002 Restrictive Cardiomyopathy 52 0.022
792
c CNT048 Central Hypoventilation Syndrome 52 0.022
793
PRT029 Parathyroid Adenoma 52 0.022
794
GRW007 Growth Hormone Deficiency 52 0.022
795
c CMP058 Complex Regional Pain Syndrome Type 1 51 0.022
796
FML164 Familial Hdl Deficiency 51 0.022
797
c DNT009 Dentin Dysplasia 51 0.022
798
MYC005 Myocardial Stunning 51 0.022
799
ACS001 Acoustic Neuroma 51 0.022
800
KMR001 Kimura Disease 51 0.022
801
SHR001 Short Bowel Syndrome 51 0.022
802
MCL003 Macular Holes 51 0.022
803
DGS001 Degos Disease 51 0.022
804
PRG008 Paragonimiasis 51 0.022
805
CLN015 Colon Adenocarcinoma 51 0.022
806
c DRR001 Diarrhea 51 0.022
807
WBR001 Weber Syndrome 51 0.022
808
P CST002 Castleman's Disease 50 0.022
809
LPR001 Lepromatous Leprosy 50 0.022
810
RTN001 Retinal Vasculitis 50 0.022
811
GST060 Gastric Cancer, Somatic 50 0.022
812
c CRB126 Cerebral Cavernous Malformation 50 0.022
813
P INT063 Intellectual Disability 50 0.022
814
PRT026 Parotitis 50 0.022
815
P LCT002 Lactose Intolerance 49 0.022
816
LGN002 Legionellosis 49 0.022
817
ERY017 Erythema Elevatum Diutinum 49 0.022
818
c EPS003 Episodic Ataxia 49 0.022
819
DVR002 Diverticulitis 49 0.022
820
TLN003 Telangiectasis 49 0.022
821
c INT060 Intestinal Atresia 49 0.022
822
TRN044 Transposition of the Great Arteries 49 0.022
823
CNV002 Conversion Disorder 49 0.022
824
c HYP011 Hyperlipoproteinemia Type Iii 49 0.022
825
c CNT035 Central Nervous System Disease 49 0.022
826
INF058 Inflammatory Myofibroblastic Tumor 48 0.022
827
CRT049 Critical Limb Ischemia 48 0.022
828
c ACT150 Acute Adrenal Insufficiency 48 0.022
829
PLM010 Pulmonary Edema 48 0.022
830
IMP002 Imperforate Anus 48 0.022
831
BRN014 Bronchopneumonia 48 0.022
832
PNC033 Pancreas Adenocarcinoma 47 0.022
833
GNT031 Genitopatellar Syndrome 47 0.022
834
CRN027 Corneal Neovascularization 47 0.022
835
NNT016 Neonatal Hemochromatosis 47 0.022
836
PRN021 Paranasal Sinus Disease 47 0.022
837
CRT008 Carotid Artery Dissection 47 0.022
838
MNC006 Monoclonal Gammopathy of Uncertain Significance 47 0.022
839
P OVR046 Ovarian Cyst 47 0.022
840
c MLG086 Malignant Hyperthermia Susceptibility 47 0.022
841
SPL004 Splenic Marginal Zone Lymphoma 47 0.022
842
MYS001 Myositis Ossificans 47 0.022
843
P TRN034 Transverse Myelitis 47 0.022
844
PPT005 Peptic Ulcer Disease 46 0.022
845
TBR008 Tuberculous Peritonitis 46 0.022
846
MNN009 Meningoencephalitis 46 0.022
847
SCR024 Sacrococcygeal Teratoma 46 0.022
848
SPL018 Splenomegaly 46 0.022
849
SML026 Small Fiber Neuropathy 45 0.022
850
PLM052 Pulmonary Arteriovenous Malformation 45 0.022
851
QBC001 Quebec Platelet Disorder 45 0.022
852
HYP054 Hypochromic Anemia 45 0.022
853
MNN017 Mononeuropathy 45 0.022
854
BWN003 Bowenoid Papulosis 45 0.022
855
WLL004 Wallerian Degeneration 45 0.022
856
DFN221 Deafness Dystonia Syndrome 45 0.022
857
ART004 Aortic Atherosclerosis 45 0.022
858
NRL007 Neurologic Diseases 45 0.022
859
INF034 Infective Endocarditis 45 0.022
860
LYM012 Lymphoplasmacytic Lymphoma 44 0.022
861
HRS011 Horseshoe Kidney 44 0.022
862
LYM011 Lymphogranuloma Venereum 44 0.022
863
c APH002 Aphasia 44 0.022
864
NNT020 Neonatal Intrahepatic Cholestasis Caused by Citrin Deficiency 44 0.022
865
CRB088 Cerebral Atrophy 44 0.022
866
SYN036 Syncope 44 0.022
867
ANP005 Anaplastic Astrocytoma 44 0.022
868
UTR024 Uterine Carcinosarcoma 44 0.022
869
PLC005 Placental Insufficiency 43 0.022
870
FTT001 Fatty Liver Disease 43 0.022
871
RTC005 Reticulosarcoma 43 0.022
872
CRB004 Cerebral Artery Occlusion 43 0.022
873
CHR010 Chorioangioma 43 0.022
874
ADN027 Adenomyosis 43 0.022
875
CRN030 Coronary Stenosis 43 0.022
876
P SZR006 Seizure Disorder 43 0.022
877
PLR005 Pleuropneumonia 43 0.022
878
CHN015 Chondrodysplasia 43 0.022
879
DFC001 Defective Apolipoprotein B-100 42 0.022
880
LMB052 Lumbar Disc Herniation 42 0.022
881
INT071 Intestinal Perforation 42 0.022
882
RBF001 Riboflavin Deficiency 42 0.022
883
ESP002 Esophageal Varix 42 0.022
884
UTR039 Uterine Fibroid 42 0.022
885
NWB001 Newborn Respiratory Distress Syndrome 41 0.022
886
c CHR342 Chiari Malformation 41 0.022
887
CRD016 Cardiac Rupture 41 0.022
888
XNT001 Xanthogranulomatous Pyelonephritis 41 0.022
889
P MYH004 Myh9 Related Thrombocytopenia 41 0.022
890
STR037 Stress Cardiomyopathy 41 0.022
891
HMT018 Hematopoietic Stem Cell Transplantation 40 0.022
892
P DPH016 Diaphragmatic Hernia 3 40 0.022
893
BLR015 Blue Rubber Bleb Nevus Syndrome 40 0.022
894
GLY015 Glycine N-Methyltransferase Deficiency 40 0.022
895
c TYP002 Type Vi Ehlers-Danlos Syndrome 40 0.022
896
MCK002 Meckel's Diverticulum 40 0.022
897
HMP018 Hemophilic Arthropathy 40 0.022
898
ACL001 Acalculous Cholecystitis 40 0.022
899
P MNN007 Meningocele 40 0.022
900
INP001 Inappropriate Adh Syndrome 40 0.022
901
GST040 Gastric Adenocarcinoma 40 0.022
902
PRT086 Partial Hydatidiform Mole 40 0.022
903
LNS001 Lens Subluxation 39 0.022
904
c PNC102 Pancreatitis, Chronic 39 0.022
905
KDN015 Kidney Angiomyolipoma 39 0.022
906
P THR045 Thrombotic Thrombocytopenic Purpura, Congenital 39 0.022
907
WTH001 Withdrawal Disorder 39 0.022
908
P CHR038 Chronic Maxillary Sinusitis 39 0.022
909
PLY024 Polymicrogyria 39 0.022
910
WRF001 Warfarin Resistance 39 0.022
911
P BRN035 Brain Stem Glioma 39 0.022
912
ART012 Aortitis 39 0.022
913
ALC005 Alcoholic Pancreatitis 39 0.022
914
TBR006 Tuberculoid Leprosy 39 0.022
915
BRN055 Bronchogenic Cyst 38 0.022
916
CHL061 Childhood Leukemia 38 0.022
917
c JVN024 Juvenile Hereditary Hemochromatosis 38 0.022
918
ADN002 Adenoiditis 38 0.022
919
SPR066 Superficial Siderosis 38 0.022
920
VTM001 Vitamin K Deficiency Hemorrhagic Disease 37 0.022
921
ERY045 Erythrocytosis, Somatic 37 0.022
922
SGN002 Signet Ring Cell Adenocarcinoma 37 0.022
923
DXT002 Dextrocardia with Situs Inversus 37 0.022
924
IMR001 Imerslund-Grasbeck Syndrome 37 0.022
925
P SYS007 Systemic Capillary Leak Syndrome 37 0.022
926
P HYP071 Hypersensitivity Reaction Type Ii Disease 37 0.022
927
CTR003 Citrin Deficiency 37 0.022
928
OPT006 Optic Nerve Disease 37 0.022
929
FTD001 Foot Drop 37 0.022
930
IPX001 Ipex Syndrome 37 0.022
931
CMB021 Combined Pituitary Hormone Deficiency 36 0.022
932
MYL046 Myelodysplastic Syndrome, Somatic 36 0.022
933
HYP143 Hypomyelination and Congenital Cataract 36 0.022
934
CNG069 Congenital Cytomegalovirus 36 0.022
935
PRL008 Paralytic Ileus 36 0.022
936
PTT021 Pituitary Hormone Deficiency, Combined 2 35 0.022
937
c FML162 Familial Mediterranean Fever, Ad 35 0.022
938
FTL012 Fetal and Neonatal Alloimmune Thrombocytopenia 35 0.022
939
NRS005 Neurosarcoidosis 35 0.022
940
INT042 Internuclear Ophthalmoplegia 34 0.022
941
LKM059 Leukemia, Megakaryoblastic, with or Without Down Syndrome, Somatic 34 0.022
942
SPR007 Superior Mesenteric Artery Syndrome 34 0.022
943
RHS001 Rh Isoimmunization 33 0.022
944
HMG020 Hmg Coa Lyase Deficiency 33 0.022
945
P ANG041 Angioedema, Hereditary, Types I and Ii 33 0.022
946
ANG049 Angioedema Induced by Ace Inhibitors 33 0.022
947
c SVR057 Severe Hemophilia B 32 0.022
948
c HRD066 Hereditary Angioedema Type Iii 32 0.022
949
ULN001 Ulnar Neuropathy 32 0.022
950
CNG219 Congenital Aural Atresia 31 0.022
951
TST021 Testicular Germ Cell Tumor 31 0.022
952
P CHR454 Chiari Malformation Type 1 31 0.022
953
c TWN006 Twin Twin Transfusion Syndrome 30 0.022
954
MGL023 Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome, Somatic 30 0.022
955
CNG134 Congenitally Corrected Transposition of the Great Arteries 30 0.022
956
SPL007 Splenic Abscess 30 0.022
957
PNG002 Pain Agnosia 30 0.022
958
P CMM008 Communicating Hydrocephalus 30 0.022
959
PRN037 Prinzmetal's Variant Angina 30 0.022
960
CRN185 Craniofacial Deafness Hand Syndrome 30 0.022
961
GLM037 Glioma Somatic 30 0.022
962
CRT028 Cor Triatriatum 29 0.022
963
P MGS003 Meigs Syndrome 29 0.022
964
SBC014 Subclavian Steal Syndrome 29 0.022
965
P 49X002 49,xxxxy Syndrome 28 0.022
966
DYS003 Dysgraphia 28 0.022
967
ADT003 Auditory System Disease 28 0.022
968
HMX002 Heme Oxygenase-1 Deficiency 28 0.022
969
P DCR004 Dacryocystitis 28 0.022
970
NRC019 Neurocutaneous Melanosis, Somatic 28 0.022
971
BLD052 Blood Group Incompatibility 28 0.022
972
GNT005 Giant Hemangioma 27 0.022
973
CRT045 Creatine Phosphokinase, Elevated Serum 27 0.022
974
INT147 Intrauterine Growth Restriction, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 27 0.022
975
SPR032 Superficial Siderosis of the Central Nervous System 27 0.022
976
CRN019 Coronary Artery Vasospasm 26 0.022
977
RHB020 Rhabdomyosarcoma, Somatic 26 0.022
978
CHR034 Chromophobe Adenoma 26 0.022
979
CPL011 Capillary Malformations, Congenital, 1, Somatic, Mosaic 26 0.022
980
P CHR097 Chronic Purulent Otitis Media 26 0.022
981
NTR005 Nutritional Deficiency Disease 25 0.022
982
MCR216 Microcephaly with or Without Chorioretinopathy, Lymphedema, or Mental Retardation 25 0.022
983
ANT013 Anterior Spinal Artery Syndrome 25 0.022
984
c MLD014 Mild Hemophilia B 25 0.022
985
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 25 0.022
986
ABD002 Abducens Nerve Disease 25 0.022
987
PRN007 Perinephritis 24 0.022
988
EMB002 Embryoma 24 0.022
989
P FML179 Familial Erythrocytosis 2 24 0.022
990
HMR039 Hemorrhage, Intracerebral 23 0.022
991
MSN002 Mesenteric Lymphadenitis 23 0.022
992
SBS002 Substernal Goiter 23 0.022
993
ANG022 Angel Shaped Phalangoepiphyseal Dysplasia 23 0.022
994
c PST001 Posterior Myocardial Infarction 23 0.022
995
MLT037 Multifocal Lymphangioendotheliomatosis with Thrombocytopenia 22 0.022
996
VRT001 Vertebral Artery Occlusion 22 0.022
997
MYX006 Myxoid Leiomyosarcoma 22 0.022
998
PRP021 Peripheral Nervous System Neoplasm 21 0.022
999
PLY004 Polyp of Corpus Uteri 21 0.022
1000
P HMN004 Hemangioma of Liver 20 0.022
1001
SBC002 Subclavian Artery Aneurysm 20 0.022
1002
PLS001 Pulsating Exophthalmos 20 0.022
1003
FXL001 Foix-Alajouanine Syndrome 20 0.022
1004
P OCL041 Oculomotor Apraxia Cogan Type 20 0.022
1005
QLT001 Qualitative Platelet Defect 20 0.022
1006
RHM007 Rheumatic Congestive Heart Failure 20 0.022
1007
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 19 0.022
1008
HYP015 Hyperlucent Lung 19 0.022
1009
CHR076 Choriocarcinoma of the Testis 19 0.022
1010
FRN014 Fournier Gangrene 19 0.022
1011
MNG003 Mungan Syndrome 19 0.022
1012
BNT001 Banti's Syndrome 19 0.022
1013
PNT023 Pontine Hemorrhage 18 0.022
1014
INT010 Intracranial Embolism 18 0.022
1015
ART109 Arterial Thoracic Outlet Syndrome 18 0.022
1016
CNT067 Central Cord Syndrome 18 0.022
1017
CRD023 Cardiomyopathy Cataract Hip Spine Disease 17 0.022
1018
CNG298 Congenital Pancreatic Cyst 17 0.022
1019
48X002 48,xxxy Syndrome 17 0.022
1020
RNL001 Renal Artery Obstruction 17 0.022
1021
CNG092 Congenital Extrahepatic Portosystemic Shunt 16 0.022
1022
OTP003 Oto-Palatal-Digital Syndrome 16 0.022
1023
DRL001 Dural Sinus Malformation 15 0.022
1024
XLN139 X-Linked Intellectual Disability - Macrocephaly - Macroorchidism 15 0.022
1025
TMP006 Temporomandibular Ankylosis 15 0.022
1026
BLT017 Bilateral Massive Adrenal Hemorrhage 15 0.022
1027
GST016 Gastric Signet Ring Cell Adenocarcinoma 14 0.022
1028
CVR001 Cavernous Sinus Meningioma 13 0.022
1029
EPT015 Epitheliopathy, Acute Posterior Multifocal Placoid Pigment 13 0.022
1030
INF001 Infarct of Liver 13 0.022
1031
CNG171 Congenital Plasminogen Deficiency 13 0.022
1032
c THR081 Thrombophilia Due to Factor V Leiden 12 0.022
1033
CYS035 Cystic Adventitial Disease 12 0.022
1034
STR080 Stroke, Hemorrhagic 11 0.022
1035
MGL021 Megalencephaly-Capillary Malformation Syndrome 11 0.022
1036
SVR055 Severe Immune-Mediated Enteropathy 11 0.022
1037
c EHL052 Ehlers–danlos Syndrome, Vascular Type 10 0.022
1038
INT055 Intravascular Fasciitis 10 0.022
1039
c PRT053 Portal Hypertension Due to Infrahepatic Block 4 0.022