Search results for Aspirin

1316 hits were found for Aspirin

# Family MCID Name MIFTS Score
1
AST052 Asthma, Nasal Polyps, and Aspirin Intolerance 39 9.414
2
ASP030 Aspirin Resistance 42 6.563
3
ASP036 Aspirin Allergy 32 3.725
4
PLT019 Platelet Disorder, Familial, with Associated Myeloid Malignancy 38 2.471
5
ISC004 Ischemia 62 0.520
6
CRB039 Cerebrovascular Disease 71 0.508
7
P CRN018 Coronary Artery Anomaly 67 0.504
8
ART140 Arteries, Anomalies of 60 0.475
9
STR067 Stroke, Ischemic 82 0.474
10
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.467
11
P MYC007 Myocardial Infarction 74 0.448
12
P CRN300 Coronary Heart Disease 1 59 0.416
13
c PRC016 Pre-Eclampsia 63 0.396
14
P CLR023 Colorectal Cancer 100 0.384
15
THR024 Thrombosis 58 0.362
16
P VSC007 Vascular Disease 65 0.359
17
AST005 Asthma 80 0.345
18
ALL026 Allergic Hypersensitivity Disease 65 0.323
19
TRN015 Transient Cerebral Ischemia 62 0.323
20
INT007 Intermediate Coronary Syndrome 58 0.316
21
PPT005 Peptic Ulcer Disease 60 0.307
22
P HRT032 Heart Disease 78 0.292
23
c ACT075 Acute Myocardial Infarction 59 0.291
24
P ATR011 Atrial Fibrillation 67 0.290
25
P URT039 Urticaria 61 0.287
26
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 36 0.286
27
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.272
28
PRP027 Peripheral Vascular Disease 72 0.270
29
P ECL001 Eclampsia 53 0.269
30
ATH013 Atherosclerosis Susceptibility 68 0.262
31
c THR092 Thrombophilia Due to Thrombin Defect 74 0.236
32
P DBT009 Diabetes Mellitus 66 0.230
33
GST023 Gastric Ulcer 53 0.230
34
P RHN004 Rhinitis 59 0.229
35
ADN018 Adenoma 60 0.224
36
PLM033 Pulmonary Embolism 60 0.223
37
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.220
38
PRP080 Peripheral Artery Disease 51 0.212
39
ANG054 Angina Pectoris 66 0.208
40
ACT058 Active Peptic Ulcer Disease 55 0.208
41
c HYP595 Hypertension, Essential 87 0.204
42
RYS001 Reye Syndrome 49 0.202
43
P KDN018 Kidney Disease 73 0.201
44
CLR108 Colorectal Adenoma 64 0.200
45
P ANG015 Angioedema 54 0.200
46
P BLD124 Bleeding Disorder, Platelet-Type, 11 66 0.198
47
c MGR028 Migraine with or Without Aura 1 70 0.197
48
c RHB024 Rhabdomyosarcoma 2 64 0.196
49
P ANT006 Antiphospholipid Syndrome 56 0.189
50
CNG034 Congestive Heart Failure 69 0.188
51
HLC007 Helicobacter Pylori Infection 61 0.186
52
P GST044 Gastritis 58 0.182
53
CLP006 Clopidogrel Resistance 41 0.176
54
P DDN001 Duodenal Ulcer 50 0.175
55
P RHM011 Rheumatoid Arthritis 82 0.174
56
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.170
57
DYS014 Dyspepsia 51 0.170
58
KWS002 Kawasaki Disease 65 0.165
59
48X005 48,xyyy 37 0.164
60
P ART022 Arthritis 71 0.163
61
P PRS040 Prostate Cancer 97 0.158
62
P THR014 Thrombocytopenia 67 0.158
63
P TRN020 Turner Syndrome 66 0.156
64
P HDC001 Headache 59 0.156
65
LPD008 Lipid Metabolism Disorder 64 0.154
66
P CTR002 Cataract 62 0.152
67
c HYP836 Hypercholesterolemia, Familial, 1 74 0.151
68
c FML001 Familial Atrial Fibrillation 67 0.151
69
P ESS003 Essential Thrombocythemia 69 0.150
70
ANR040 Aneurysm 60 0.150
71
c LRG017 Large Intestine Cancer 53 0.148
72
c CHR684 Chronic Kidney Disease 68 0.147
73
CRT013 Carotid Stenosis 50 0.145
74
P HYP098 Hypereosinophilic Syndrome 67 0.143
75
P ADN016 Adenocarcinoma 65 0.143
76
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.143
77
PNG002 Pain Agnosia 52 0.143
78
IGR001 Ige Responsiveness, Atopic 61 0.141
79
P PNC035 Pancreatic Cancer 86 0.140
80
ATX019 Ataxia with Vitamin E Deficiency 46 0.140
81
OST012 Osteoarthritis 80 0.138
82
ADL002 Adult Syndrome 62 0.138
83
P BRS047 Breast Cancer 99 0.135
84
P EXN002 Exanthem 58 0.135
85
RHM027 Rheumatic Disease 56 0.135
86
CRN017 Coronary Thrombosis 45 0.134
87
c ACT210 Acute Respiratory Distress Syndrome 59 0.132
88
P PRC031 Preeclampsia/eclampsia 1 42 0.132
90
P RSP003 Respiratory Failure 75 0.129
91
CYT002 Cytokine Deficiency 46 0.128
92
P MCR115 Microvascular Complications of Diabetes 5 67 0.126
93
P THR015 Thrombophilia 51 0.124
94
P GST053 Gastric Cancer 85 0.123
95
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.123
96
LMB062 Limb Ischemia 50 0.123
97
P LNG032 Lung Cancer 99 0.121
98
P OVR042 Ovarian Cancer 89 0.119
99
c SYS001 Systemic Lupus Erythematosus 88 0.119
100
P LVR013 Liver Disease 71 0.119
101
P PLY018 Polycythemia 56 0.119
102
P ART021 Arteriosclerosis 56 0.119
103
THR004 Thrombocytosis 52 0.119
104
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.118
105
PLY001 Polycythemia Vera 70 0.118
106
PLC008 Placenta Disease 51 0.116
107
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.116
108
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.116
109
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.116
110
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.116
111
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.116
112
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.116
113
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.116
114
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.116
115
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.116
116
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.116
117
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.116
118
P PRG092 Pregnancy Loss, Recurrent 1 40 0.116
119
ESP021 Esophageal Cancer 90 0.114
120
P LYN001 Lynch Syndrome 77 0.114
121
c SVR005 Severe Pre-Eclampsia 50 0.114
122
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.112
123
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.110
124
P FML011 Familial Adenomatous Polyposis 73 0.110
125
ALL003 Allergic Rhinitis 69 0.110
126
P LPS004 Lupus Erythematosus 62 0.110
127
ENT004 Enthesopathy 46 0.110
128
P HPT023 Hepatocellular Carcinoma 99 0.109
129
P ESP024 Esophagitis 62 0.109
130
P DRR001 Diarrhea 55 0.109
131
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.109
132
BRR014 Barrett Esophagus 67 0.107
133
INT002 Intermittent Claudication 60 0.107
134
P PRD008 Periodontitis 66 0.105
135
CRN030 Coronary Stenosis 49 0.105
136
PLC007 Placental Abruption 47 0.105
137
P NTR004 Neutropenia 64 0.103
138
HYP066 Hyperglycemia 63 0.103
139
DFC004 Deficiency Anemia 77 0.101
140
HMR039 Hemorrhage, Intracerebral 59 0.101
141
PPL001 Papillary Adenoma 42 0.101
142
c PRS136 Prostate Cancer, Hereditary, 6 34 0.101
143
c PRS130 Prostate Cancer, Hereditary, 8 33 0.101
144
CMM005 Common Cold 57 0.099
145
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.099
146
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.099
147
P RCT021 Rectum Cancer 54 0.099
148
DWN001 Down Syndrome 70 0.097
149
MYL069 Myeloma, Multiple 85 0.095
150
ATM095 Autoimmune Disease 62 0.095
151
RHM001 Rheumatic Fever 56 0.095
152
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.095
153
P BLD134 Bladder Cancer 79 0.092
154
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.092
155
P END033 Endocarditis 58 0.092
156
END057 Endometrial Cancer 74 0.090
157
GST092 Gastroesophageal Reflux 68 0.090
158
P VSC011 Vasculitis 64 0.090
159
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.090
160
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.090
161
INT030 Intracranial Aneurysm 57 0.090
162
RSP006 Respiratory System Disease 57 0.090
163
47X002 47,xyy 49 0.090
164
c MCR120 Microvascular Complications of Diabetes 7 48 0.090
165
VTM033 Vitamin K Deficiency Bleeding 47 0.090
166
RRS014 Rare Surgical Neurologic Disease 33 0.090
167
P DMN002 Dementia 68 0.088
168
c MCR113 Microvascular Complications of Diabetes 3 55 0.088
169
c MCR130 Microvascular Complications of Diabetes 6 42 0.088
170
c MCR133 Microvascular Complications of Diabetes 4 42 0.088
171
EXR007 Exercise-Induced Anaphylaxis 25 0.088
172
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 20 0.088
173
CLN015 Colon Adenocarcinoma 65 0.086
174
P VNW001 Von Willebrand's Disease 64 0.086
175
VSC002 Vascular Dementia 57 0.086
176
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.086
177
PRP030 Purpura 56 0.086
178
P HMR003 Hemorrhagic Disease 54 0.086
179
c CHR048 Chronic Rhinitis 42 0.086
180
P MLT020 Multiple Sclerosis 73 0.083
181
MLN008 Melanoma 68 0.083
182
LVR012 Liver Cirrhosis 67 0.083
183
P SKN015 Skin Carcinoma 67 0.083
184
DPR016 Depression 64 0.083
185
HYP266 Hypoxia 58 0.083
186
AGN016 Aging 58 0.083
187
INF034 Infective Endocarditis 53 0.083
188
P ERY008 Erythromelalgia 44 0.083
189
CRB086 Cerebral Aneurysms 41 0.083
190
P CRD119 Cardiac Arrest 71 0.081
191
MNT002 Mental Depression 60 0.081
192
PRC013 Pericarditis 54 0.081
193
OCL069 Ocular Motor Apraxia 53 0.081
194
P CRN074 Coronary Artery Aneurysm 47 0.081
195
CRB004 Cerebral Artery Occlusion 38 0.081
196
c SML038 Small Cell Cancer of the Lung 67 0.078
197
c ACT071 Acute Kidney Failure 60 0.078
198
P INF032 Infertility 60 0.078
199
CRT016 Carotid Artery Disease 53 0.078
200
GSG001 Gas Gangrene 52 0.078
201
BLD053 Blood Platelet Disease 51 0.078
202
CRD137 Cardiogenic Shock 50 0.078
203
PLT015 Platelet Aggregation, Spontaneous 40 0.078
204
P ALZ034 Alzheimer Disease 90 0.075
205
c ART115 Aortic Valve Disease 1 76 0.075
206
HMN044 Human Immunodeficiency Virus Type 1 73 0.075
207
CHL065 Cholangiocarcinoma 68 0.075
208
c JVN010 Juvenile Rheumatoid Arthritis 67 0.075
209
GT001 Gout 63 0.075
210
c BRN108 Branchiootic Syndrome 1 62 0.075
211
END030 End Stage Renal Failure 60 0.075
212
GST033 Gestational Diabetes 58 0.075
213
P NRP001 Neuropathy 57 0.075
214
P CHR345 Chronic Pain 52 0.075
215
P RNV001 Renovascular Hypertension 49 0.075
216
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.075
217
RCK004 Rickets 70 0.073
218
P PLM037 Pulmonary Hypertension 69 0.073
219
P HPT021 Hepatitis 69 0.073
220
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.073
221
HYP056 Hypoglycemia 68 0.073
222
c MCR129 Microvascular Complications of Diabetes 1 67 0.073
223
P MNN013 Meningitis 67 0.073
224
MYL031 Myeloproliferative Neoplasm 66 0.073
225
TXC005 Toxic Shock Syndrome 63 0.073
226
P KDN017 Kidney Cancer 60 0.073
227
P BPL003 Bipolar Disorder 59 0.073
228
CMR002 Coumarin Resistance 56 0.073
229
c PRD040 Periodontitis, Chronic 56 0.073
230
RHM028 Rheumatic Heart Disease 54 0.073
231
INT079 Intrahepatic Cholangiocarcinoma 54 0.073
232
BRN071 Brain Injury 51 0.073
233
TBR011 Tuberculous Meningitis 50 0.073
234
BWN001 Bowen-Conradi Syndrome 49 0.073
235
c HYP272 Hypercholesterolemia, Familial, 3 44 0.073
236
BCK006 Back Pain 44 0.073
237
c MJR024 Major Affective Disorder 9 42 0.073
238
c MCR112 Microvascular Complications of Diabetes 2 42 0.073
239
c MJR022 Major Affective Disorder 8 39 0.073
241
GLB002 Glioblastoma 74 0.070
242
PRT036 Peritonitis 66 0.070
243
c FNC043 Fanconi Anemia, Complementation Group E 64 0.070
244
KHL003 Kohlschutter-Tonz Syndrome 63 0.070
245
PRT013 Portal Hypertension 61 0.070
246
GLB015 Glioblastoma Multiforme 60 0.070
247
P SZR006 Seizure Disorder 59 0.070
248
P HMP007 Hemophilia 58 0.070
249
PLM010 Pulmonary Edema 56 0.070
250
HRT012 Heart Valve Disease 56 0.070
251
PLC005 Placental Insufficiency 55 0.070
252
TRM010 Traumatic Brain Injury 54 0.070
253
c GLL024 Gallbladder Disease 1 53 0.070
254
P SCK005 Sickle Cell Disease 53 0.070
255
HDN002 Head Injury 47 0.070
256
RRD056 Rare Disease in Surgical Orthopedic 29 0.070
257
ART016 Aortic Aneurysm 71 0.067
258
MYL005 Myelofibrosis 69 0.067
259
P DRM053 Dermatitis, Atopic 68 0.067
260
CHG001 Chagas Disease 66 0.067
261
CLT003 Colitis 63 0.067
262
c PNS012 Paine Syndrome 61 0.067
263
P ADL010 Adult Respiratory Distress Syndrome 61 0.067
264
SQM006 Squamous Cell Carcinoma 60 0.067
265
P LYM031 Lymphocytic Leukemia 56 0.067
266
IMM064 Immunodeficiency, Common Variable, 10 51 0.067
267
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.067
269
c PLM164 Pulmonary Hypertension, Primary, 1 79 0.064
270
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.064
271
c ART101 Aortic Valve Disease 2 67 0.064
272
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.064
273
P GLM045 Glioma 64 0.064
274
P HYP750 Hypertriglyceridemia, Familial 62 0.064
275
ACQ007 Acquired Immunodeficiency Syndrome 61 0.064
276
P BCL017 B-Cell Lymphoma 61 0.064
277
P THR005 Thrombotic Thrombocytopenic Purpura 59 0.064
278
VSL002 Visual Epilepsy 58 0.064
279
DSS009 Disseminated Intravascular Coagulation 58 0.064
280
ALL006 Allergic Asthma 56 0.064
281
CHC001 Chickenpox 53 0.064
282
FDL002 Food Allergy 52 0.064
283
CLN045 Colonic Benign Neoplasm 52 0.064
284
BNR002 Bone Resorption Disease 51 0.064
285
GLS018 Glass Syndrome 51 0.064
286
GLL048 Glial Tumor 48 0.064
287
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.064
288
CRN006 Coronary Aneurysm 35 0.064
289
CYT018 Cytochrome P450 2d6 Variant 28 0.064
290
CRV035 Cervical Cancer 77 0.061
291
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.061
292
TBC004 Tobacco Addiction 65 0.061
293
FTT001 Fatty Liver Disease 63 0.061
294
LNG099 Lung Disease 62 0.061
295
P SNS001 Sensorineural Hearing Loss 62 0.061
296
P PNC044 Pancreatitis 61 0.061
297
P CRD132 Cardiac Conduction Defect 61 0.061
298
EYD002 Eye Disease 59 0.061
299
P OPT006 Optic Nerve Disease 59 0.061
300
IRN002 Iron Metabolism Disease 58 0.061
301
PTN001 Patent Foramen Ovale 57 0.061
302
PHR003 Pharyngitis 56 0.061
303
HYP005 Hypokalemia 55 0.061
304
LNG031 Lung Benign Neoplasm 52 0.061
305
RTN003 Retinal Ischemia 52 0.061
306
STR039 Sturge-Weber Syndrome 52 0.061
307
P RTN022 Retinal Vein Occlusion 50 0.061
308
GST049 Gastrointestinal System Cancer 49 0.061
309
RTN020 Retinal Vascular Disease 49 0.061
310
INT010 Intracranial Embolism 47 0.061
311
GST071 Gastrointestinal Carcinoma 42 0.061
312
OVR094 Ovarian Epithelial Cancer 39 0.061
313
c SYS043 Systemic Lupus Erythematosus 1 39 0.061
314
CRT004 Carotid Artery Thrombosis 37 0.061
315
INT040 Intrinsic Asthma 34 0.061
316
IMM167 Immune Deficiency Disease 79 0.057
317
c ATR087 Atrial Standstill 1 76 0.057
318
SCK003 Sickle Cell Anemia 74 0.057
319
P CNR004 Cone-Rod Dystrophy 2 72 0.057
320
P MYC084 Mycobacterium Tuberculosis 1 69 0.057
321
P MJR001 Major Depressive Disorder 69 0.057
322
P HRP006 Herpes Simplex 66 0.057
323
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.057
324
c LYN004 Lynch Syndrome I 61 0.057
325
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.057
326
CNS004 Constipation 59 0.057
327
P GLM007 Glomerulonephritis 58 0.057
328
NWB001 Newborn Respiratory Distress Syndrome 58 0.057
329
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 58 0.057
330
HRP004 Herpes Zoster 58 0.057
331
INT078 Intracranial Thrombosis 48 0.057
332
BNM001 Bone Marrow Cancer 48 0.057
333
c THR090 Thrombocythemia 1 47 0.057
334
PPT001 Peptic Esophagitis 47 0.057
335
ENT001 Enterocele 44 0.057
336
PST053 Postherpetic Neuralgia 43 0.057
337
DBT008 Diabetic Angiopathy 42 0.057
338
TRP009 Triple X Syndrome 42 0.057
339
NRL016 Neural Tube Defects 83 0.053
340
P OST002 Osteoporosis 79 0.053
341
ULC004 Ulcerative Colitis 75 0.053
342
CRH001 Crohn's Disease 75 0.053
343
ANX010 Anxiety 75 0.053
344
SVR004 Severe Combined Immunodeficiency 74 0.053
345
c SPN225 Spondyloarthropathy 1 74 0.053
346
P PNM007 Pneumonia 71 0.053
347
BRN024 Bronchitis 70 0.053
348
LYM133 Lymphoma, Hodgkin, Classic 70 0.053
349
P LKM002 Leukemia 69 0.053
350
P HYD006 Hydrocephalus 68 0.053
351
SKN019 Skin Melanoma 68 0.053
352
OST159 Osteogenic Sarcoma 67 0.053
353
P ENC018 Encephalopathy 64 0.053
354
DRM006 Dermatitis 63 0.053
355
P PSR002 Psoriasis 63 0.053
356
OVR029 Ovarian Hyperstimulation Syndrome 63 0.053
357
MDD011 Mood Disorder 62 0.053
358
P THL005 Thalassemia 62 0.053
359
NRL005 Neurilemmoma 62 0.053
360
c ART138 Aortic Aneurysm, Familial Abdominal, 1 62 0.053
361
NTR005 Nutritional Deficiency Disease 61 0.053
362
VRC005 Varicose Veins 61 0.053
363
CHL014 Cholera 58 0.053
364
TNS005 Tonsillitis 58 0.053
365
GST050 Gastrointestinal System Disease 57 0.053
366
ACS001 Acoustic Neuroma 57 0.053
367
P FBR017 Fibrosarcoma 57 0.053
368
c FML035 Familial Hyperlipidemia 56 0.053
369
c CNG216 Congenital Hydrocephalus 55 0.053
370
GLC003 Glucose Intolerance 55 0.053
371
IMP005 Impotence 53 0.053
372
HLL004 Hellp Syndrome 53 0.053
373
HMT008 Hematuria, Benign Familial 53 0.053
374
DYS073 Dysphagia 52 0.053
375
HRT011 Heart Septal Defect 52 0.053
376
PST011 Pustulosis of Palm and Sole 51 0.053
377
PRT018 Portal Vein Thrombosis 50 0.053
378
ECT026 Ectopic Pregnancy 50 0.053
379
WTH001 Withdrawal Disorder 47 0.053
380
DDN006 Duodenitis 44 0.053
381
AGR002 Agoraphobia 44 0.053
382
MCR011 Microinvasive Gastric Cancer 43 0.053
383
MMM006 Mammographic Density 43 0.053
384
GNG003 Gingival Recession 43 0.053
386
WBR001 Weber Syndrome 35 0.053
387
c LKM071 Leukemia, Chronic Lymphocytic 81 0.049
388
P LNG064 Lung Cancer Susceptibility 3 79 0.049
389
P SCH015 Schizophrenia 76 0.049
390
P LYM118 Lymphoma 70 0.049
391
SRC014 Sarcoma 67 0.049
392
P CNJ013 Conjunctivitis 67 0.049
393
GST040 Gastric Adenocarcinoma 67 0.049
394
P NRB010 Neuroblastoma 1 66 0.049
395
P OCL013 Oculodentodigital Dysplasia 65 0.049
396
P HML002 Hemolytic Anemia 64 0.049
397
P VNT002 Ventricular Septal Defect 61 0.049
398
GNG013 Gingivitis 60 0.049
399
P INF037 Inflammatory Bowel Disease 57 0.049
400
BCT022 Bacterial Infectious Disease 57 0.049
401
SFT003 Soft Tissue Sarcoma 57 0.049
402
HYP060 Hyperinsulinism 55 0.049
403
HMC014 Homocysteinemia 54 0.049
404
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 54 0.049
405
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 53 0.049
406
HYP014 Hyperuricemia 52 0.049
407
c PRM012 Primary Polycythemia 52 0.049
408
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.049
409
STM007 Stomatitis 51 0.049
410
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 48 0.049
411
P ART018 Aortic Valve Insufficiency 47 0.049
412
CRB008 Cerebral Atherosclerosis 47 0.049
413
SYN036 Syncope 46 0.049
414
P RTN014 Retinal Artery Occlusion 46 0.049
415
MYC005 Myocardial Stunning 45 0.049
416
IDP033 Idiopathic Edema 44 0.049
417
P MJR007 Major Affective Disorder 1 44 0.049
418
DRG024 Drug Allergy 43 0.049
419
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.049
420
BRN026 Branch Retinal Artery Occlusion 41 0.049
421
PPT002 Peptic Ulcer Perforation 37 0.049
422
AMR003 Amaurosis Fugax 36 0.049
423
c LKM004 Leukemia, B-Cell, Chronic 35 0.049
425
CHL079 Children's Interstitial Lung Disease 27 0.049
426
CYS001 Cystic Fibrosis 84 0.045
427
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.045
428
P EPL164 Epilepsy 73 0.045
429
P HYP086 Hypothyroidism 70 0.045
430
KRT019 Keratitis, Hereditary 69 0.045
431
CNN005 Connective Tissue Disease 68 0.045
432
P LKM062 Leukemia, Acute Lymphoblastic 68 0.045
433
PSY004 Psychotic Disorder 68 0.045
434
P NSP012 Nasopharyngeal Carcinoma 67 0.045
435
PRT037 Pertussis 66 0.045
436
DSS008 Disease of Mental Health 66 0.045
437
INC002 Inclusion Body Myositis 66 0.045
438
MSC007 Muscle Hypertrophy 65 0.045
439
P NPH012 Nephrotic Syndrome 65 0.045
440
PSR001 Psoriatic Arthritis 63 0.045
441
SPN186 Spinal Cord Injury 63 0.045
442
c PRG042 Progressive Familial Heart Block, Type Ia 62 0.045
443
CHL068 Cholestasis 61 0.045
444
ING001 Inguinal Hernia 61 0.045
445
c ACT027 Acute Pancreatitis 60 0.045
446
GST045 Gastroenteritis 60 0.045
447
IRN001 Iron Deficiency Anemia 59 0.045
448
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.045
449
P TRC086 Trichohepatoenteric Syndrome 1 57 0.045
450
SPN035 Spindle Cell Sarcoma 57 0.045
451
HMN014 Human Immunodeficiency Virus Infectious Disease 56 0.045
452
P INT068 Intestinal Disease 56 0.045
453
GRN034 Grange Syndrome 55 0.045
454
P HYP076 Hyperthyroidism 55 0.045
455
P MYS005 Myositis 54 0.045
456
P PNC025 Panic Disorder 53 0.045
457
P CHL066 Cholangitis 53 0.045
458
P RTN018 Retinal Disease 53 0.045
459
P MGR003 Migraine with Aura 53 0.045
460
NNL006 Non-Alcoholic Steatohepatitis 53 0.045
461
P AGG001 Aggressive Periodontitis 50 0.045
462
c MLG074 Malignant Mesenchymoma 50 0.045
463
P IDP024 Idiopathic Inflammatory Myopathy 49 0.045
464
SCH003 Schizophreniform Disorder 49 0.045
465
SPL018 Splenomegaly 48 0.045
466
MTB004 Metabolic Acidosis 48 0.045
467
HYP781 Hypoascorbemia 48 0.045
468
P MGR001 Migraine Without Aura 47 0.045
469
P HMR005 Hemorrhoid 47 0.045
470
ACT017 Acute Chest Syndrome 47 0.045
471
HRT015 Heritable Pulmonary Arterial Hypertension 46 0.045
472
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 46 0.045
473
c PRM038 Primary Agammaglobulinemia 45 0.045
474
c PCH010 Pachyonychia Congenita 3 43 0.045
475
DBT007 Diabetic Cataract 42 0.045
476
CLN044 Colon Adenoma 41 0.045
477
49X002 49,xxxxy Syndrome 39 0.045
478
c MJR008 Major Affective Disorder 2 35 0.045
479
c MJR003 Major Affective Disorder 6 34 0.045
480
c MJR006 Major Affective Disorder 5 34 0.045
481
c MJR023 Major Affective Disorder 7 34 0.045
482
SNG003 Single Ventricular Heart 31 0.045
483
FNT004 Fainting 31 0.045
484
RSP007 Respiratory Distress Syndrome, Infant 31 0.045
485
c MJR004 Major Affective Disorder 4 29 0.045
486
P OVR096 Overlap Myositis 28 0.045
487
ACT094 Acute Articular Rheumatism 27 0.045
488
CRT084 Creatinine Clearance Quantitative Trait Locus 26 0.045
489
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.040
490
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.040
491
P TBR001 Tuberous Sclerosis 72 0.040
492
c FML346 Familial Adenomatous Polyposis 1 71 0.040
493
c TBR026 Tuberous Sclerosis 2 69 0.040
494
P INF038 Influenza 69 0.040
495
c BSL007 Basal Cell Carcinoma 68 0.040
496
c DPH024 Diaphragmatic Hernia, Congenital 66 0.040
497
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 65 0.040
498
FCT007 Factor Vii Deficiency 65 0.040
499
c HPT016 Hepatitis B 63 0.040
500
P MYP004 Myopathy 63 0.040
501
OST003 Osteonecrosis 62 0.040
502
VRL011 Viral Infectious Disease 62 0.040
503
CRD223 Cardiac Arrhythmia 61 0.040
504
STT001 Status Epilepticus 61 0.040
505
P ATR010 Atrial Heart Septal Defect 61 0.040
506
CHL123 Chlamydia 60 0.040
507
c LPM012 Lipomatosis, Multiple 60 0.040
508
P MYC008 Myocarditis 60 0.040
509
c ACT073 Acute Leukemia 59 0.040
510
P CYS018 Cystitis 59 0.040
511
RNL024 Renal Glucosuria 59 0.040
512
P BRS044 Breast Adenocarcinoma 59 0.040
513
P PLY011 Polycystic Ovary Syndrome 58 0.040
514
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.040
515
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.040
516
RLP002 Relapsing-Remitting Multiple Sclerosis 57 0.040
517
c VRL010 Viral Hepatitis 56 0.040
518
SYN007 Synovitis 55 0.040
519
END040 Endogenous Depression 55 0.040
520
CLN019 Colonic Disease 55 0.040
521
P ESP035 Esophagitis, Eosinophilic, 1 54 0.040
522
FCT001 Factor Viii Deficiency 54 0.040
523
c SCN036 Secondary Progressive Multiple Sclerosis 54 0.040
524
AMN001 Amenorrhea 54 0.040
525
PLM017 Pulmonary Alveolar Microlithiasis 54 0.040
526
SPN051 Spondylitis 53 0.040
527
KRT006 Keratoconjunctivitis 53 0.040
528
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.040
529
PRT082 Preterm Premature Rupture of the Membranes 53 0.040
530
BRN038 Bronchial Disease 53 0.040
531
NRT001 Neurotic Disorder 53 0.040
532
CHR073 Choreatic Disease 52 0.040
533
IMM136 Immune System Disease 52 0.040
534
GST009 Gastroschisis 52 0.040
535
GST037 Gastroparesis 52 0.040
536
MCL006 Macular Retinal Edema 52 0.040
537
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.040
538
P PRC012 Pericardial Effusion 51 0.040
539
CLR109 Colorectal Adenocarcinoma 51 0.040
540
URM002 Uremia 50 0.040
541
NRM004 Neuroma 50 0.040
542
INT253 Intestinal Benign Neoplasm 50 0.040
543
P OPN001 Open-Angle Glaucoma 50 0.040
544
NRL018 Neural Tube Defects, Folate-Sensitive 50 0.040
545
PLR008 Pleurisy 50 0.040
546
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 49 0.040
547
NTR046 Neutrophil Migration 49 0.040
548
c MTR002 Mitral Valve Insufficiency 49 0.040
549
VRN004 Vernal Keratoconjunctivitis 49 0.040
550
HPR003 Heparin-Induced Thrombocytopenia 49 0.040
551
CHR001 Churg-Strauss Syndrome 48 0.040
552
P BLD051 Blood Coagulation Disease 48 0.040
553
CRN019 Coronary Artery Vasospasm 48 0.040
554
BHR001 Behr Syndrome 47 0.040
555
ESN020 Eosinophilic Granulomatosis with Polyangiitis 47 0.040
556
LFT001 Left Bundle Branch Hemiblock 47 0.040
557
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 46 0.040
558
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 45 0.040
559
ASP026 Asplenia, Isolated Congenital 45 0.040
560
CRT015 Carotid Artery Occlusion 44 0.040
561
HMP001 Hemopericardium 44 0.040
562
THR035 Thrombasthenia 42 0.040
563
ANG049 Angioedema Induced by Ace Inhibitors 41 0.040
564
THR123 Thrombotic Microangiopathy 41 0.040
565
c CNT028 Central Retinal Artery Occlusion 40 0.040
566
CRN020 Coronary Restenosis 40 0.040
567
c HYP555 Hypertriglyceridemia, Transient Infantile 38 0.040
568
ANG065 Angioma, Tufted 38 0.040
569
ABD010 Abdominal Wall Defect 37 0.040
570
c CHR682 Chronic Bilirubin Encephalopathy 36 0.040
571
INT003 Intracranial Hypotension 34 0.040
572
DDN004 Duodenogastric Reflux 31 0.040
573
c MYC058 Myocardial Infarction 2 30 0.040
574
INF009 Inflammatory Spondylopathy 29 0.040
575
c CRN214 Coronary Heart Disease 5 25 0.040
576
INT074 Intracranial Arteriosclerosis 17 0.040
577
P ATX030 Ataxia-Telangiectasia 83 0.035
578
SQM013 Squamous Cell Carcinoma, Head and Neck 81 0.035
579
P PRK057 Parkinson Disease, Late-Onset 77 0.035
580
P NRF023 Neurofibromatosis, Type Ii 77 0.035
581
BRN028 Brain Cancer 75 0.035
582
RNL065 Renal Cell Carcinoma, Papillary, 1 75 0.035
583
c HPT073 Hepatitis C Virus 74 0.035
584
c TBR025 Tuberous Sclerosis 1 74 0.035
585
c NRF024 Neurofibromatosis, Type I 72 0.035
586
P SLP006 Sleep Apnea 71 0.035
587
MLT157 Multiple System Atrophy 1 71 0.035
588
CRB037 Cerebral Palsy 69 0.035
589
PNC129 Pancreatic Adenocarcinoma 69 0.035
590
P SYS005 Systemic Scleroderma 68 0.035
591
P GLM040 Glioma Susceptibility 1 68 0.035
592
P LPR021 Leprosy 3 67 0.035
593
LYM007 Lymphangioleiomyomatosis 67 0.035
594
CLF027 Cleft Palate, Isolated 67 0.035
595
NRF026 Neurofibromatosis, Type Iv, of Riccardi 65 0.035
596
ANR007 Anorexia Nervosa 64 0.035
597
FLL027 Fallopian Tube Carcinoma 64 0.035
598
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.035
599
APN008 Apnea, Obstructive Sleep 64 0.035
600
P ANR048 Aniridia 1 64 0.035
601
NRF007 Neurofibroma 63 0.035
602
P ART005 Arteriovenous Malformation 63 0.035
603
c ACT068 Acute Cystitis 63 0.035
604
c ALP101 Alpha-Thalassemia 63 0.035
605
RTN017 Retinal Detachment 62 0.035
606
c HPT001 Hepatitis C 62 0.035
607
ACN002 Acanthosis Nigricans 62 0.035
608
P CND004 Candidiasis 61 0.035
609
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 61 0.035
610
SPP011 Suppression of Tumorigenicity 12 61 0.035
611
PRT058 Pure Autonomic Failure 60 0.035
612
P PTN014 Patent Ductus Arteriosus 1 60 0.035
613
HPT019 Hepatic Encephalopathy 60 0.035
614
ARG002 Argininosuccinic Aciduria 59 0.035
615
P MYP006 Myopia 58 0.035
616
c THY109 Thyroid Cancer, Nonmedullary, 1 58 0.035
617
c PRX059 Peroxisome Biogenesis Disorder 1a 57 0.035
618
PLS011 Plasmacytoma 57 0.035
619
ANT009 Antithrombin Iii Deficiency 57 0.035
620
P SCK002 Sick Sinus Syndrome 56 0.035
621
ATR057 Atrioventricular Block 56 0.035
622
P LTR001 Lateral Sclerosis 56 0.035
623
SNS003 Sensory Peripheral Neuropathy 56 0.035
624
P VNS003 Venous Insufficiency 55 0.035
625
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 54 0.035
626
HMT018 Hematopoietic Stem Cell Transplantation 54 0.035
627
P MMB011 Membranous Nephropathy 54 0.035
628
INT075 Intracranial Hypertension 54 0.035
629
P HML001 Hemolytic-Uremic Syndrome 54 0.035
630
P MTR003 Mitral Valve Stenosis 54 0.035
631
P HYP838 Hyperlipidemia, Familial Combined, 3 54 0.035
632
HMS001 Hemosiderosis 54 0.035
633
SPP010 Suppressor of Tumorigenicity 3 54 0.035
634
EXP004 Exophthalmos 53 0.035
635
OLG003 Oligohydramnios 53 0.035
636
FRZ001 Frozen Shoulder 53 0.035
637
P TMP001 Temporal Lobe Epilepsy 53 0.035
638
CLF001 Cleft Lip 53 0.035
639
MMM001 Mammary Paget's Disease 53 0.035
640
c HYP740 Hyperlipoproteinemia, Type V 53 0.035
641
LMY002 Leiomyoma 52 0.035
642
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.035
643
DNT012 Dental Caries 52 0.035
644
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.035
645
c INH020 Inherited Metabolic Disorder 51 0.035
646
P MND003 Mandibuloacral Dysplasia with Type a Lipodystrophy 51 0.035
647
PRT014 Protein S Deficiency 50 0.035
648
RYN005 Raynaud Phenomenon 50 0.035
649
THR016 Thrombophlebitis 50 0.035
650
c INF145 Infantile Liver Failure Syndrome 1 50 0.035
651
P ATR005 Atrophic Gastritis 49 0.035
652
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.035
653
THR013 Thoracic Outlet Syndrome 49 0.035
654
HYL004 Hyaline Fibromatosis Syndrome 49 0.035
655
MTP025 Metaphyseal Chondrodysplasia, Schmid Type 48 0.035
656
c CHR431 Chronic Venous Insufficiency 48 0.035
657
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 48 0.035
658
STT002 Status Asthmaticus 47 0.035
659
ART004 Aortic Atherosclerosis 47 0.035
660
GRN017 Granulocytopenia 46 0.035
661
P HRN001 Horner's Syndrome 46 0.035
662
HMR002 Hemarthrosis 46 0.035
663
KRT013 Keratolytic Winter Erythema 45 0.035
664
TND005 Tendinitis 45 0.035
665
KHN001 Kuhnt-Junius Degeneration 45 0.035
666
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.035
667
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 44 0.035
668
c EST002 Estrogen-Receptor Negative Breast Cancer 43 0.035
669
KPS002 Kaposiform Hemangioendothelioma 43 0.035
670
c AVS006 Avascular Necrosis of Femoral Head, Primary, 1 43 0.035
671
SYS003 Systolic Heart Failure 43 0.035
672
SBC016 Subacute Delirium 43 0.035
673
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.035
674
BRS064 Bursitis 42 0.035
675
HPT004 Hepatic Coma 42 0.035
676
RDN001 Reading Disorder 42 0.035
677
HMN016 Hemangioendothelioma 41 0.035
678
PLS016 Plasma Cell Leukemia 41 0.035
679
ALL014 Allergic Encephalomyelitis 40 0.035
680
HPT082 Hepatic Adenomas, Familial 40 0.035
681
CRD170 Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 1 40 0.035
682
HRP025 Herpes Simplex Virus Keratitis 40 0.035
683
ADP007 Adie Pupil 40 0.035
684
c HMG029 Hemoglobin Se Disease 40 0.035
685
c OVR114 Ovarian Cancer 1 39 0.035
686
GNR003 Generalized Atherosclerosis 39 0.035
687
SPR126 Superior Semicircular Canal Dehiscence 39 0.035
688
VRN001 Vernal Conjunctivitis 39 0.035
689
LVD003 Livedoid Vasculitis 39 0.035
690
RCT017 Rectal Disease 39 0.035
691
CHL147 Chlamydia Pneumonia 39 0.035
692
ATX010 Ataxia Neuropathy Spectrum 39 0.035
693
EXT006 Extrahepatic Cholestasis 38 0.035
694
THR017 Thoracoabdominal Syndrome 38 0.035
695
ATM052 Autoimmune Disease 1 38 0.035
696
ANS012 Anus Disease 37 0.035
697
PSD088 Pseudobulbar Affect 37 0.035
698
OPT010 Optic Papillitis 37 0.035
699
P ANT001 Anterolateral Myocardial Infarction 37 0.035
700
BRR002 Barrett's Adenocarcinoma 36 0.035
701
CRT008 Carotid Artery Dissection 36 0.035
702
NCR002 Necrobiosis Lipoidica 36 0.035
703
MDD003 Middle Cerebral Artery Infarction 35 0.035
704
HNS001 Hansen's Disease 35 0.035
705
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.035
706
P VSC018 Visceral Steatosis 34 0.035
707
DDN009 Duodenal Obstruction 33 0.035
708
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 32 0.035
709
MTP028 Metaphyseal Dysplasia, Spahr Type 32 0.035
710
INF118 Inflammatory Myopathy with Abundant Macrophages 29 0.035
711
PLT031 Platelet Membrane Fluidity 29 0.035
712
P ACT232 Acute Necrotizing Encephalopathy 28 0.035
713
c HYP839 Hyperlipidemia, Familial Combined, 1 28 0.035
714
CHR669 Chromosome 2p16.3 Deletion Syndrome 27 0.035
715
HNM002 Hinman Syndrome 26 0.035
716
FTL073 Fetal Anticonvulsant Syndrome 26 0.035
717
ATR055 Atrial Septal Aneurysm 25 0.035
718
ALL012 Allergic Angiitis 25 0.035
719
MNS002 Mini Stroke 20 0.035
720
BLD137 Blood Group--Ahonen 17 0.035
721
c LKM061 Leukemia, Acute Myeloid 84 0.029
722
c DLT002 Dilated Cardiomyopathy 81 0.029
723
c MNN043 Meningioma, Familial 74 0.029
724
c LKM063 Leukemia, Chronic Myeloid 74 0.029
725
LPT014 Leptin Deficiency or Dysfunction 72 0.029
726
P AMY004 Amyloidosis 71 0.029
727
P MLN066 Melanoma, Cutaneous Malignant 1 69 0.029
728
c HMP029 Hemophilia a 69 0.029
729
ALC007 Alcohol Dependence 68 0.029
730
P NRV007 Nervous System Disease 68 0.029
731
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 67 0.029
732
P FLL037 Follicular Lymphoma 67 0.029
733
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.029
734
GLN010 Glanzmann Thrombasthenia 66 0.029
735
UND005 Undifferentiated Pleomorphic Sarcoma 66 0.029
736
P PLM036 Pulmonary Fibrosis 66 0.029
737
AND002 Androgen Insensitivity Syndrome 66 0.029
738
P ANG001 Angelman Syndrome 65 0.029
739
IDP011 Idiopathic Interstitial Pneumonia 65 0.029
740
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 65 0.029
741
IRR002 Irritable Bowel Syndrome 65 0.029
742
P PRP019 Peripheral Nervous System Disease 64 0.029
743
P THY023 Thymoma 64 0.029
744
MNN042 Meningioma, Radiation-Induced 64 0.029
745
HMT002 Hematologic Cancer 64 0.029
746
LWC002 Lowe Oculocerebrorenal Syndrome 63 0.029
747
ART002 Arts Syndrome 63 0.029
748
P ACR001 Aicardi-Goutieres Syndrome 63 0.029
749
c SYS004 Systemic Mastocytosis 63 0.029
750
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 63 0.029
751
ALP103 Alpha-1-Antitrypsin Deficiency 63 0.029
752
P MST009 Mastocytosis 62 0.029
753
P ART067 Aortic Aneurysm, Familial Thoracic 1 62 0.029
754
c SCL052 Scleroderma, Familial Progressive 62 0.029
755
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 62 0.029
756
c THR082 Thrombophilia Due to Activated Protein C Resistance 61 0.029
757
CRY035 Cryptorchidism, Unilateral or Bilateral 61 0.029
759
APP008 Appendicitis 61 0.029
760
THR100 Thrombocytopenic Purpura, Autoimmune 61 0.029
761
CHL067 Cholecystitis 60 0.029
762
ART001 Arterial Tortuosity Syndrome 60 0.029
763
P BRN022 Bronchiectasis 60 0.029
764
P EHL001 Ehlers-Danlos Syndrome 60 0.029
765
c HRD002 Hereditary Angioedema 59 0.029
766
P PGT001 Paget's Disease of Bone 59 0.029
767
c PTT056 Pituitary Adenoma 1, Multiple Types 59 0.029
768
P SYP003 Syphilis 59 0.029
769
c MST023 Mesothelioma, Malignant 59 0.029
770
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 58 0.029
771
P UVT001 Uveitis 58 0.029
772
P ALP008 Alopecia 58 0.029
773
CYT008 Cytomegalovirus Infection 58 0.029
774
P ALC033 Alcohol Use Disorder 58 0.029
775
P AXN002 Axenfeld-Rieger Syndrome 58 0.029
776
BRG013 Buerger Disease 58 0.029
777
ERY051 Erythroleukemia, Familial 58 0.029
778
ERY029 Erythermalgia, Primary 58 0.029
779
P PRN023 Prion Disease 57 0.029
780
GLL018 Gallbladder Cancer 57 0.029
781
TRN018 Transitional Cell Carcinoma 57 0.029
782
HMG005 Hemoglobinopathy 57 0.029
783
BRN004 Brain Edema 57 0.029
784
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.029
785
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 56 0.029
786
ALV005 Alveolar Soft Part Sarcoma 56 0.029
787
P SHR029 Short Syndrome 56 0.029
788
MCS002 Mucositis 56 0.029
789
DFF005 Diffuse Large B-Cell Lymphoma 56 0.029
790
PPL022 Papilloma 56 0.029
791
P PLM034 Pulmonary Emphysema 55 0.029
792
P ALP106 Alport Syndrome 1, X-Linked 55 0.029
793
c THY107 Thymoma, Familial 55 0.029
794
c PSR017 Psoriasis 2 55 0.029
795
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 55 0.029
796
P SML001 Small Cell Carcinoma 55 0.029
797
c GRV008 Graves Disease 1 55 0.029
798
P OPT009 Optic Neuritis 55 0.029
799
PRS045 Prostatic Hypertrophy 55 0.029
800
P INS002 in Situ Carcinoma 55 0.029
801
PRP016 Paraplegia 54 0.029
802
FCT004 Factor Xii Deficiency 54 0.029
803
MMB001 Membranoproliferative Glomerulonephritis 54 0.029
804
ZLL002 Zollinger-Ellison Syndrome 54 0.029
805
P HYP083 Hypopituitarism 53 0.029
806
TLN003 Telangiectasis 53 0.029
807
P UTR058 Uterine Anomalies 53 0.029
808
CHR100 Chronic Ulcer of Skin 53 0.029
809
c ACR116 Aicardi-Goutieres Syndrome 1 53 0.029
810
P MYM013 Moyamoya Disease 1 53 0.029
811
P THY032 Thyroiditis 52 0.029
812
NRT004 Neuritis 52 0.029
813
PRS021 Prostatic Adenoma 52 0.029
814
P MYT002 Myotonic Dystrophy 52 0.029
815
RDC002 Radiculopathy 51 0.029
816
ILS001 Ileus 51 0.029
817
HYP081 Hypolipoproteinemia 51 0.029
818
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.029
819
HYP063 Hypersplenism 51 0.029
820
P PST095 Post-Thrombotic Syndrome 50 0.029
821
c PSR023 Psoriasis 1 50 0.029
822
P ESN008 Eosinophilic Pneumonia 50 0.029
823
IGG001 Iga Glomerulonephritis 50 0.029
824
PRS129 Prostatic Hyperplasia, Benign 49 0.029
825
RNL077 Renal Fibrosis 49 0.029
826
c PRG126 Progressive Familial Heart Block 49 0.029
827
PRD004 Prediabetes Syndrome 49 0.029
828
SKN013 Skin Benign Neoplasm 49 0.029
829
c ANT034 Anterior Uveitis 48 0.029
830
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 48 0.029
831
KRT002 Keratomalacia 47 0.029
832
MGS001 Megaesophagus 47 0.029
833
PYL006 Pyloric Stenosis 47 0.029
834
P BNG032 Benign Mesothelioma 47 0.029
835
FBR019 Fibromatosis 47 0.029
836
P RNL015 Renal Hypertension 47 0.029
837
MCL027 Macular Dystrophy, Dominant Cystoid 47 0.029
838
INT067 Interstitial Nephritis 46 0.029
839
P CLL015 Collagen Disease 46 0.029
840
NWC001 Newcastle Disease 45 0.029
841
c DYS119 Dystonia 9 45 0.029
842
STR089 Storage Pool Platelet Disease 45 0.029
843
BLR013 Biliary Tract Cancer 44 0.029
844
P OCY003 Oocyte Maturation Defect 1 44 0.029
845
RFR003 Refractive Error 44 0.029
846
CLL014 Cll/sll 44 0.029
847
TND004 Tendinopathy 44 0.029
848
CNN010 Connective Tissue Benign Neoplasm 44 0.029
849
BNS003 Binswanger's Disease 43 0.029
850
ORL012 Oral Leukoplakia 42 0.029
851
RTN021 Retinal Vascular Occlusion 42 0.029
852
P CRN035 Cranial Nerve Palsy 42 0.029
853
ACT003 Acute Kidney Tubular Necrosis 42 0.029
854
HYP540 Hypertension, Diastolic 41 0.029
855
SNL007 Senile Cataract 41 0.029
856
RTN004 Retinal Microaneurysm 41 0.029
857
P RRH023 Rare Hereditary Hemochromatosis 41 0.029
858
LKP003 Leukoplakia 40 0.029
859
UTR043 Uterine Sarcoma 40 0.029
860
ART008 Arteriosclerosis Obliterans 40 0.029
861
SPN021 Spinal Meningioma 40 0.029
862
FST001 Foster-Kennedy Syndrome 40 0.029
863
LYM002 Lymphoplasmacyte-Rich Meningioma 40 0.029
864
c PSR028 Psoriasis 7 40 0.029
865
LCH001 Leech Infestation 40 0.029
866
c PSR018 Psoriasis 13 40 0.029
867
c PSR032 Psoriasis 11 40 0.029
868
C1N001 C1 Inhibitor Deficiency 39 0.029
869
P TRC005 Tracheal Stenosis 39 0.029
870
HYP189 Hypoadrenalism 39 0.029
871
SPS057 Spasticity 38 0.029
872
MNN021 Meningococcemia 38 0.029
873
SCR001 Secretory Meningioma 38 0.029
874
c ATM022 Autoimmune Myocarditis 36 0.029
875
HRW001 Hair Whorl 36 0.029
876
OST062 Osteoarthritis with Mild Chondrodysplasia 36 0.029
877
END072 Endotheliitis 36 0.029
878
SBC014 Subclavian Steal Syndrome 36 0.029
879
MLG141 Malignant Atrophic Papulosis 34 0.029
880
c ATM104 Autoimmune Vasculitis 33 0.029
881
RNL001 Renal Artery Obstruction 33 0.029
882
TTH007 Tooth Erosion 32 0.029
883
CYT004 Cytomegalic Inclusion Disease 32 0.029
884
ALR002 Al-Raqad Syndrome 32 0.029
885
GST029 Gastric Cardia Adenocarcinoma 31 0.029
887
PRC051 Paracetamol Poisoning 31 0.029
888
AMN014 Aminopterin Syndrome Sine Aminopterin 30 0.029
889
UND007 Undifferentiated Connective Tissue Disease 30 0.029
890
ORL006 Oral Mucosa Leukoplakia 27 0.029
891
MYT026 Myotonia Atrophica 25 0.029
892
BLD163 Blood Group, Dombrock System 24 0.029
893
MSC026 Muscular Dystrophy White Matter Spongiosis 16 0.029
894
APC006 Apc-Associated Polyposis Conditions 12 0.029
895
INS024 Insulin-Like Growth Factor I 79 0.020
896
CNN003 Conn's Syndrome 78 0.020
897
GST019 Gastrointestinal Stromal Tumor 76 0.020
898
P RTN024 Retinoblastoma 74 0.020
899
c BTT014 Beta-Thalassemia 73 0.020
900
ADR007 Adrenoleukodystrophy 72 0.020
901
P HNT016 Huntington Disease 72 0.020
902
PLM001 Pulmonary Tuberculosis 72 0.020
903
OTT002 Otitis Media 71 0.020
904
c MLT156 Multiple Endocrine Neoplasia, Type I 71 0.020
905
P GRF003 Graft-Versus-Host Disease 71 0.020
906
ADN011 Adenoid Cystic Carcinoma 71 0.020
907
P PHC003 Pheochromocytoma 71 0.020
908
ACR007 Acromegaly 70 0.020
909
P TTR001 Tetralogy of Fallot 70 0.020
910
BSL036 Basal Cell Nevus Syndrome 70 0.020
911
P FML018 Familial Mediterranean Fever 70 0.020
912
P TMP003 Temporal Arteritis 68 0.020
913
c MYT021 Myotonic Dystrophy 1 68 0.020
914
ADR054 Adrenocortical Carcinoma, Hereditary 68 0.020
915
c HML033 Hemolytic Uremic Syndrome, Atypical 1 67 0.020
916
P PRM011 Primary Ciliary Dyskinesia 67 0.020
917
P ASP006 Aspergillosis 67 0.020
918
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.020
919
c HMP004 Hemophilia B 66 0.020
920
P PRS038 Personality Disorder 66 0.020
921
P BLD062 Bile Duct Cancer 66 0.020
922
c INF071 Inflammatory Bowel Disease 1 66 0.020
923
P HRD008 Hereditary Hemorrhagic Telangiectasia 64 0.020
924
END041 Endometrial Adenocarcinoma 64 0.020
925
P HRM001 Hermansky-Pudlak Syndrome 64 0.020
926
P CMP005 Campomelic Dysplasia 64 0.020
927
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 63 0.020
928
HSH003 Hashimoto Thyroiditis 63 0.020
929
BLL006 Bullous Pemphigoid 63 0.020
930
P NRN021 Neuronal Ceroid Lipofuscinosis 63 0.020
931
P LMY004 Leiomyosarcoma 63 0.020
932
P MVM001 Movement Disease 63 0.020
933
c GLC092 Glaucoma, Primary Open Angle 63 0.020
934
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 63 0.020
935
P END044 Endometriosis 63 0.020
936
P HYP055 Hypoplastic Left Heart Syndrome 63 0.020
937
MCR013 Microphthalmia 62 0.020
938
P RHB003 Rhabdomyosarcoma 62 0.020
939
BLD131 Bladder Urothelial Carcinoma 62 0.020
940
BDD001 Budd-Chiari Syndrome 62 0.020
941
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 62 0.020
942
CRC021 Carcinosarcoma 62 0.020
943
ORL011 Oral Cancer 62 0.020
944
THY029 Thyroid Carcinoma 62 0.020
945
TYP007 Typhoid Fever 61 0.020
946
DGR001 Digeorge Syndrome 61 0.020
947
c DNG003 Dengue Disease 61 0.020
948
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 61 0.020
949
ETN001 Eating Disorder 61 0.020
950
P ART023 Arthropathy 61 0.020
951
P MYL006 Myeloid Leukemia 61 0.020
952
MSL001 Measles 61 0.020
953
LNG073 Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 61 0.020
954
P BRN019 Bernard-Soulier Syndrome 60 0.020
955
ORN008 Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to 60 0.020
956
LGG001 Legg-Calve-Perthes Disease 60 0.020
957
BND020 Bone Disease 60 0.020
958
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 60 0.020
959
P MLT074 Multiple Endocrine Neoplasia 59 0.020
960
P HRD011 Hereditary Spherocytosis 59 0.020
961
FCT002 Factor Xi Deficiency 59 0.020
962
NRN004 Neuroendocrine Tumor 59 0.020
963
BRS051 Breast Disease 59 0.020
964
GRY002 Gray Platelet Syndrome 59 0.020
965
c CHL119 Cholangitis, Primary Sclerosing 59 0.020
966
P MTR012 Mitral Valve Disease 59 0.020
967
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 58 0.020
968
P PLY006 Polydactyly 58 0.020
969
c VNW010 Von Willebrand Disease, Type 2 58 0.020
970
EXT034 Extrinsic Allergic Alveolitis 58 0.020
971
CNT047 Contact Dermatitis 58 0.020
972
BLR008 Bilirubin Metabolic Disorder 58 0.020
973
ALK013 Alkaptonuria 57 0.020
974
LMY014 Leiomyoma, Uterine 57 0.020
975
SPN041 Spinal Cord Disease 57 0.020
976
P CHN012 Chondrosarcoma 57 0.020
977
P MLN007 Male Infertility 57 0.020
978
c ANG068 Angioedema, Hereditary, Type I 57 0.020
979
CMP010 Complex Regional Pain Syndrome 57 0.020
980
ALL010 Allergic Contact Dermatitis 56 0.020
981
P BNC003 Bone Cancer 56 0.020
982
CRH005 Crohn's Colitis 56 0.020
983
FLR002 Filariasis 56 0.020
984
BLM002 Bulimia Nervosa 56 0.020
985
P RTN016 Retinal Degeneration 56 0.020
986
P FTL001 Fetal Alcohol Syndrome 56 0.020
987
P FNC044 Fanconi Anemia, Complementation Group C 56 0.020
988
DBT010 Diabetic Neuropathy 56 0.020
989
HNC001 Henoch-Schoenlein Purpura 56 0.020
990
CRN239 Carnitine Deficiency, Systemic Primary 56 0.020
991
HPT046 Hepatic Veno-Occlusive Disease 56 0.020
992
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 56 0.020
993
EHL052 Ehlers-Danlos Syndrome, Vascular Type 56 0.020
994
P SBS003 Substance Abuse 56 0.020
995
ORP003 Oropharynx Cancer 55 0.020
996
CRN295 Carnitine Palmitoyltransferase I Deficiency 55 0.020
997
ANN002 Anencephaly 55 0.020
998
CHK001 Chikungunya 55 0.020
999
c THR045 Thrombotic Thrombocytopenic Purpura, Congenital 55 0.020
1000
MST005 Mastitis 55 0.020
1001
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 55 0.020
1002
MTC027 Mitochondrial Trifunctional Protein Deficiency 55 0.020
1003
P TRM003 Tremor 55 0.020
1004
CLF004 Cleft Lip/palate 55 0.020
1005
PRN019 Perinatal Necrotizing Enterocolitis 55 0.020
1006
P OVR049 Ovarian Disease 55 0.020
1007
DCB001 Decubitus Ulcer 54 0.020
1008
P FBR031 Febrile Seizures 54 0.020
1009
P BRC006 Brachydactyly 54 0.020
1010
P RST001 Restless Legs Syndrome 54 0.020
1011
LYM040 Lymphoblastic Lymphoma 54 0.020
1012
TXC002 Toxic Encephalopathy 54 0.020
1013
ACY005 Acyl-Coa Dehydrogenase, Short-Chain, Deficiency of 54 0.020
1014
DMY004 Demyelinating Disease 54 0.020
1015
P HYP040 Hypospadias 54 0.020
1016
PRP036 Peripheral T-Cell Lymphoma 53 0.020
1017
P LRY019 Laryngitis 53 0.020
1018
c ACT134 Acute Liver Failure 53 0.020
1019
c HYP841 Hypoalphalipoproteinemia, Primary, 1 53 0.020
1020
P ATN002 Autonomic Nervous System Disease 52 0.020
1021
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 52 0.020
1022
LYS002 Lysosomal Storage Disease 52 0.020
1023
INT303 Intracranial Hypertension, Idiopathic 52 0.020
1024
P MNC007 Monocytic Leukemia 52 0.020
1025
FML037 Female Breast Cancer 52 0.020
1026
P LCT001 Lactic Acidosis 52 0.020
1027
P AST007 Astrocytoma 52 0.020
1028
SRS001 Serous Cystadenocarcinoma 51 0.020
1029
P SML016 Small Intestine Cancer 51 0.020
1030
OVR082 Overgrowth Syndrome 51 0.020
1031
PST021 Postpartum Depression 51 0.020
1032
ENT011 Enterocolitis 51 0.020
1033
FLR001 Filarial Elephantiasis 51 0.020
1034
c XNT010 Xanthinuria, Type I 51 0.020
1035
APL002 Aplasia of Lacrimal and Salivary Glands 51 0.020
1036
AMB002 Amblyopia 51 0.020
1037
3MT001 3-Methylcrotonyl-Coa Carboxylase Deficiency 51 0.020
1038
P OMP004 Omphalocele 51 0.020
1039
P ALP061 Alopecia, Androgenetic, 1 51 0.020
1040
ADR040 Adrenal Gland Pheochromocytoma 51 0.020
1041
VLV011 Vulvovaginal Candidiasis 50 0.020
1042
CHL004 Cholelithiasis 50 0.020
1043
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 50 0.020
1044
SCB001 Scabies 50 0.020
1045
SCH012 Schizoaffective Disorder 50 0.020
1046
VCC001 Vaccinia 50 0.020
1047
ACR041 Acromelic Frontonasal Dysostosis 50 0.020
1048
ACH005 Achalasia 50 0.020
1049
VLC001 Velocardiofacial Syndrome 50 0.020
1050
P OVR046 Ovarian Cyst 50 0.020
1051
STM006 Stomach Disease 50 0.020
1052
LPR001 Lepromatous Leprosy 50 0.020
1053
P ALL008 Allergic Bronchopulmonary Aspergillosis 50 0.020
1054
ALL009 Allergic Conjunctivitis 50 0.020
1055
BLL003 Bell's Palsy 50 0.020
1056
SXL003 Sexual Disorder 49 0.020
1057
P LPM005 Lipomatosis 49 0.020
1058
HYD061 Hydrocephalus, Normal-Pressure 49 0.020
1059
ESP002 Esophageal Varix 49 0.020
1060
DDN011 Duodenal Atresia 49 0.020
1061
HMG002 Hemoglobinuria 49 0.020
1062
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 49 0.020
1063
HPT009 Hepatopulmonary Syndrome 49 0.020
1064
SQM002 Squamous Cell Papilloma 49 0.020
1065
c BCT013 Bacterial Pneumonia 49 0.020
1066
P ART106 Arterial Calcification, Generalized, of Infancy, 1 49 0.020
1067
c SPL067 Split-Hand/foot Malformation 1 49 0.020
1068
TRC062 Tricuspid Atresia 49 0.020
1069
RLP001 Relapsing Polychondritis 49 0.020
1070
c CNT015 Central Sleep Apnea 48 0.020
1071
CRN027 Corneal Neovascularization 48 0.020
1072
SPL012 Splenic Disease 48 0.020
1073
CCN001 Cocaine Dependence 48 0.020
1074
LYM019 Lymphosarcoma 48 0.020
1075
c HNT004 Huntington Disease-Like 2 48 0.020
1076
CLC006 Calcinosis 48 0.020
1077
c PRG043 Progressive Familial Heart Block, Type Ib 48 0.020
1078
ALB002 Albinism 48 0.020
1079
VTM002 Vitamin B12 Deficiency 48 0.020
1080
HYP017 Hypophosphatemia 48 0.020
1081
SPN020 Spondylosis 48 0.020