Search results for Aspirin

1344 hits were found for Aspirin

# Family MCID Name MIFTS Score
1
AST052 Asthma, Nasal Polyps, and Aspirin Intolerance 43 9.989
2
ASP030 Aspirin Resistance 39 6.510
3
ASP036 Aspirin Allergy 30 3.701
4
PLT019 Platelet Disorder, Familial, with Associated Myeloid Malignancy 40 2.456
5
LPP008 Lipoprotein Quantitative Trait Locus 62 0.502
6
ISC004 Ischemia 58 0.494
7
STR067 Stroke, Ischemic 81 0.471
8
ART140 Arteries, Anomalies of 52 0.465
9
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.462
10
P MYC007 Myocardial Infarction 70 0.439
11
CRB039 Cerebrovascular Disease 67 0.429
12
c PRC016 Pre-Eclampsia 63 0.411
13
P CRN300 Coronary Heart Disease 1 63 0.409
14
P CLR023 Colorectal Cancer 99 0.369
15
P VSC007 Vascular Disease 63 0.350
16
THR024 Thrombosis 57 0.349
17
AST005 Asthma 76 0.330
18
TRN015 Transient Cerebral Ischemia 63 0.322
19
INT007 Intermediate Coronary Syndrome 55 0.307
20
ALL026 Allergic Hypersensitivity Disease 62 0.299
21
PPT005 Peptic Ulcer Disease 59 0.299
22
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.287
23
c ACT075 Acute Myocardial Infarction 57 0.285
24
P ECL001 Eclampsia 50 0.281
25
P URT039 Urticaria 58 0.279
26
P ATR011 Atrial Fibrillation 66 0.276
27
P CRD246 Cardiovascular System Disease 57 0.275
28
P HRT032 Heart Disease 75 0.272
29
PRP027 Peripheral Vascular Disease 71 0.270
30
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.261
31
ATH013 Atherosclerosis Susceptibility 65 0.256
32
c THR092 Thrombophilia Due to Thrombin Defect 73 0.241
33
GST023 Gastric Ulcer 53 0.226
34
P DBT009 Diabetes Mellitus 64 0.225
35
P RHN004 Rhinitis 57 0.222
36
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.218
37
PRP080 Peripheral Artery Disease 53 0.218
38
PLM033 Pulmonary Embolism 59 0.217
39
ADN018 Adenoma 59 0.217
40
ANG054 Angina Pectoris 66 0.206
41
ACT058 Active Peptic Ulcer Disease 55 0.205
42
P KDN018 Kidney Disease 72 0.203
43
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.201
44
c HYP595 Hypertension, Essential 84 0.199
45
CLR108 Colorectal Adenoma 64 0.197
46
P ANG015 Angioedema 57 0.195
47
RYS001 Reye Syndrome 51 0.194
48
P ANT006 Antiphospholipid Syndrome 55 0.193
49
c MGR028 Migraine with or Without Aura 1 67 0.188
50
c RHB024 Rhabdomyosarcoma 2 67 0.183
51
CNG034 Congestive Heart Failure 69 0.182
52
HLC007 Helicobacter Pylori Infection 59 0.182
53
P GST044 Gastritis 56 0.179
54
KWS002 Kawasaki Disease 65 0.176
55
CLP006 Clopidogrel Resistance 40 0.171
56
P DDN001 Duodenal Ulcer 52 0.169
57
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.164
58
P PRS040 Prostate Cancer 97 0.161
59
48X005 48,xyyy 39 0.155
60
P THR014 Thrombocytopenia 67 0.153
61
LPD008 Lipid Metabolism Disorder 62 0.153
62
P ART022 Arthritis 69 0.152
63
c FML001 Familial Atrial Fibrillation 65 0.150
64
c HYP836 Hypercholesterolemia, Familial, 1 73 0.149
65
P ESS003 Essential Thrombocythemia 68 0.149
66
P TRN020 Turner Syndrome 67 0.149
67
P HDC001 Headache 57 0.149
68
P CTR002 Cataract 60 0.148
69
ANR040 Aneurysm 59 0.148
70
P PRC031 Preeclampsia/eclampsia 1 38 0.148
71
P RHM011 Rheumatoid Arthritis 80 0.145
72
c CHR684 Chronic Kidney Disease 70 0.142
73
CRT013 Carotid Stenosis 50 0.142
74
P PNC035 Pancreatic Cancer 84 0.141
75
PNG002 Pain Agnosia 51 0.140
76
P HYP098 Hypereosinophilic Syndrome 67 0.138
77
P ADN016 Adenocarcinoma 64 0.138
78
IGR001 Ige Responsiveness, Atopic 59 0.137
79
P EXN002 Exanthem 57 0.136
80
OST012 Osteoarthritis 78 0.134
81
P RSP003 Respiratory Failure 74 0.134
82
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.134
83
ATX019 Ataxia with Vitamin E Deficiency 42 0.134
84
CRN017 Coronary Thrombosis 47 0.131
85
CYT002 Cytokine Deficiency 42 0.131
86
P GST053 Gastric Cancer 83 0.130
87
LMB062 Limb Ischemia 55 0.130
88
P BRS047 Breast Cancer 97 0.128
89
ADL002 Adult Syndrome 70 0.128
91
P LNG032 Lung Cancer 98 0.125
92
P THR015 Thrombophilia 51 0.125
93
P OVR042 Ovarian Cancer 88 0.122
94
c SYS001 Systemic Lupus Erythematosus 86 0.122
95
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.122
96
P MCR115 Microvascular Complications of Diabetes 5 66 0.122
97
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.122
98
P HPT023 Hepatocellular Carcinoma 100 0.121
99
ESP021 Esophageal Cancer 90 0.121
100
P LVR013 Liver Disease 68 0.121
101
PLC008 Placenta Disease 50 0.121
102
P PLY018 Polycythemia 56 0.119
103
THR004 Thrombocytosis 51 0.119
104
P LYN001 Lynch Syndrome 77 0.117
105
PLY001 Polycythemia Vera 69 0.117
106
P ART021 Arteriosclerosis 54 0.116
107
P ESP024 Esophagitis 62 0.114
108
P LPS004 Lupus Erythematosus 61 0.112
109
c SVR005 Severe Pre-Eclampsia 50 0.112
110
P PRG092 Pregnancy Loss, Recurrent 1 40 0.112
111
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.112
112
PLC007 Placental Abruption 48 0.109
113
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.109
114
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.107
115
P FML011 Familial Adenomatous Polyposis 72 0.107
116
P PRD008 Periodontitis 64 0.107
117
INT002 Intermittent Claudication 61 0.107
118
P DRR001 Diarrhea 55 0.107
119
ENT004 Enthesopathy 49 0.107
120
ALL003 Allergic Rhinitis 67 0.105
121
BRR014 Barrett Esophagus 65 0.104
122
CMM005 Common Cold 57 0.104
123
CRN030 Coronary Stenosis 50 0.102
124
MYL069 Myeloma, Multiple 85 0.100
125
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.100
126
END057 Endometrial Cancer 74 0.100
127
DFC004 Deficiency Anemia 70 0.100
128
ATM095 Autoimmune Disease 62 0.100
129
HMR039 Hemorrhage, Intracerebral 57 0.100
130
P RCT021 Rectum Cancer 52 0.100
131
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.098
132
HYP066 Hyperglycemia 61 0.098
133
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.098
134
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.098
135
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.098
136
RSP006 Respiratory System Disease 50 0.098
137
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.098
138
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.098
139
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.098
140
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.098
141
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.098
142
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.098
143
PPL001 Papillary Adenoma 44 0.098
144
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.098
145
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.098
146
c PRS136 Prostate Cancer, Hereditary, 6 33 0.098
147
c PRS130 Prostate Cancer, Hereditary, 8 32 0.098
148
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.096
149
P END033 Endocarditis 57 0.096
150
P MLN008 Melanoma 69 0.094
151
GST092 Gastroesophageal Reflux 67 0.094
152
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.094
153
VTM033 Vitamin K Deficiency Bleeding 48 0.094
154
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.094
155
DWN001 Down Syndrome 70 0.092
156
P DMN002 Dementia 66 0.092
157
P VSC011 Vasculitis 62 0.092
158
RHM001 Rheumatic Fever 60 0.092
159
INT030 Intracranial Aneurysm 56 0.092
160
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.090
161
P NTR004 Neutropenia 63 0.090
162
P BLD134 Bladder Cancer 79 0.087
163
P INF032 Infertility 57 0.087
164
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.087
165
HYP266 Hypoxia 57 0.087
166
INF034 Infective Endocarditis 53 0.087
167
47X002 47,xyy 49 0.087
168
c MCR120 Microvascular Complications of Diabetes 7 47 0.087
169
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.087
170
EXR007 Exercise-Induced Anaphylaxis 25 0.087
171
P SKN015 Skin Carcinoma 66 0.085
172
P VNW001 Von Willebrand's Disease 65 0.085
173
CLN015 Colon Adenocarcinoma 65 0.085
174
DPR016 Depression 63 0.085
175
VSC002 Vascular Dementia 57 0.085
176
ALL006 Allergic Asthma 56 0.085
177
c MCR113 Microvascular Complications of Diabetes 3 52 0.085
178
c MCR130 Microvascular Complications of Diabetes 6 41 0.085
179
c MCR133 Microvascular Complications of Diabetes 4 41 0.085
180
CRB086 Cerebral Aneurysms 40 0.085
181
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 19 0.085
182
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.083
183
c SML038 Small Cell Cancer of the Lung 65 0.083
184
P ADL010 Adult Respiratory Distress Syndrome 65 0.083
185
LVR012 Liver Cirrhosis 62 0.083
186
MNT002 Mental Depression 58 0.083
187
PRC013 Pericarditis 54 0.083
188
CRT016 Carotid Artery Disease 52 0.083
189
c CHR048 Chronic Rhinitis 46 0.083
190
HPR006 Heparin Cofactor Ii Deficiency 40 0.083
191
P MNN013 Meningitis 66 0.081
192
MYL031 Myeloproliferative Neoplasm 66 0.081
193
c ACT071 Acute Kidney Failure 60 0.081
194
PRP030 Purpura 54 0.081
195
P HMR003 Hemorrhagic Disease 53 0.081
196
OCL069 Ocular Motor Apraxia 51 0.081
197
END086 End Stage Renal Disease 51 0.081
198
TBR011 Tuberculous Meningitis 48 0.081
199
P ERY008 Erythromelalgia 47 0.081
200
P CRN074 Coronary Artery Aneurysm 39 0.081
201
RCK004 Rickets 68 0.078
202
P CRD119 Cardiac Arrest 67 0.078
203
P NRP001 Neuropathy 56 0.078
204
CRB004 Cerebral Artery Occlusion 45 0.078
205
CVD001 Covid-19 44 0.078
206
P ALZ034 Alzheimer Disease 88 0.076
207
P MLT020 Multiple Sclerosis 72 0.076
208
HMN044 Human Immunodeficiency Virus Type 1 71 0.076
209
GT001 Gout 64 0.076
210
GST033 Gestational Diabetes 61 0.076
211
P BPL003 Bipolar Disorder 56 0.076
212
CMR002 Coumarin Resistance 56 0.076
213
GSG001 Gas Gangrene 53 0.076
214
CRD137 Cardiogenic Shock 47 0.076
215
BCK006 Back Pain 42 0.076
216
c MJR024 Major Affective Disorder 9 41 0.076
217
c MJR022 Major Affective Disorder 8 38 0.076
218
c ART115 Aortic Valve Disease 1 75 0.073
219
CHL065 Cholangiocarcinoma 68 0.073
220
c JVN010 Juvenile Rheumatoid Arthritis 64 0.073
221
c FNC043 Fanconi Anemia, Complementation Group E 62 0.073
222
c BRN108 Branchiootic Syndrome 1 62 0.073
223
BWN001 Bowen-Conradi Syndrome 52 0.073
224
P RNV001 Renovascular Hypertension 48 0.073
225
P HPT021 Hepatitis 67 0.071
226
c MCR129 Microvascular Complications of Diabetes 1 66 0.071
227
HYP056 Hypoglycemia 66 0.071
228
c DBT099 Diabetes Mellitus, Type I 65 0.071
229
TXC005 Toxic Shock Syndrome 62 0.071
230
P KDN017 Kidney Cancer 60 0.071
231
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.071
232
P SZR006 Seizure Disorder 56 0.071
233
AGN016 Aging 56 0.071
234
PLM010 Pulmonary Edema 54 0.071
235
RHM028 Rheumatic Heart Disease 53 0.071
236
c PRD040 Periodontitis, Chronic 53 0.071
237
PPT001 Peptic Esophagitis 52 0.071
238
INT079 Intrahepatic Cholangiocarcinoma 51 0.071
239
BLD053 Blood Platelet Disease 49 0.071
240
c HYP272 Hypercholesterolemia, Familial, 3 44 0.071
241
c MCR112 Microvascular Complications of Diabetes 2 41 0.071
242
c SYS043 Systemic Lupus Erythematosus 1 38 0.071
243
GLB015 Glioblastoma Multiforme 75 0.068
244
MYL005 Myelofibrosis 70 0.068
245
ART016 Aortic Aneurysm 69 0.068
246
P PNM007 Pneumonia 68 0.068
247
SKN019 Skin Melanoma 68 0.068
248
P PLM037 Pulmonary Hypertension 67 0.068
249
CHG001 Chagas Disease 66 0.068
250
P DRM053 Dermatitis, Atopic 66 0.068
251
KHL003 Kohlschutter-Tonz Syndrome 65 0.068
252
PRT036 Peritonitis 64 0.068
253
PRT013 Portal Hypertension 59 0.068
254
DSS009 Disseminated Intravascular Coagulation 57 0.068
255
PLC005 Placental Insufficiency 57 0.068
256
c GLL024 Gallbladder Disease 1 53 0.068
257
P HMP007 Hemophilia 51 0.068
258
P SCK005 Sickle Cell Disease 50 0.068
259
BRN071 Brain Injury 49 0.068
260
BNR002 Bone Resorption Disease 48 0.068
261
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.068
262
HDN002 Head Injury 46 0.068
263
P CHR345 Chronic Pain 44 0.068
264
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.065
265
P GLM045 Glioma 63 0.065
266
CLT003 Colitis 62 0.065
267
FTT001 Fatty Liver Disease 61 0.065
268
P PNC044 Pancreatitis 61 0.065
269
SQM006 Squamous Cell Carcinoma 60 0.065
270
P OPT006 Optic Nerve Disease 60 0.065
271
VSL002 Visual Epilepsy 59 0.065
272
P BCL017 B-Cell Lymphoma 58 0.065
273
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.065
274
HYP005 Hypokalemia 55 0.065
275
GST049 Gastrointestinal System Cancer 49 0.065
276
GST071 Gastrointestinal Carcinoma 47 0.065
277
GLL048 Glial Tumor 45 0.065
278
OVR094 Ovarian Epithelial Cancer 38 0.065
280
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.062
281
c ATR087 Atrial Standstill 1 75 0.062
282
P MYC084 Mycobacterium Tuberculosis 1 68 0.062
283
P MJR001 Major Depressive Disorder 68 0.062
284
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.062
285
c ART101 Aortic Valve Disease 2 65 0.062
286
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.062
287
c SVR001 Severe Acute Respiratory Syndrome 62 0.062
288
P HYP750 Hypertriglyceridemia, Familial 62 0.062
289
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.062
290
c PNS012 Paine Syndrome 61 0.062
291
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.062
292
PTN001 Patent Foramen Ovale 60 0.062
293
ACQ007 Acquired Immunodeficiency Syndrome 60 0.062
294
c LYN004 Lynch Syndrome I 60 0.062
295
CHC001 Chickenpox 60 0.062
296
CRD132 Cardiac Conduction Defect 58 0.062
297
NWB001 Newborn Respiratory Distress Syndrome 58 0.062
298
GLS018 Glass Syndrome 57 0.062
299
FDL002 Food Allergy 51 0.062
300
PLS009 Plasma Cell Neoplasm 51 0.062
301
TRM010 Traumatic Brain Injury 51 0.062
302
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.062
303
CLN045 Colonic Benign Neoplasm 46 0.062
304
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.062
305
CRN006 Coronary Aneurysm 39 0.062
306
CYT018 Cytochrome P450 2d6 Variant 27 0.062
307
CRV035 Cervical Cancer 76 0.059
308
TBC004 Tobacco Addiction 64 0.059
309
LNG099 Lung Disease 60 0.059
310
STR039 Sturge-Weber Syndrome 60 0.059
311
P SNS001 Sensorineural Hearing Loss 60 0.059
312
EYD002 Eye Disease 58 0.059
313
IRN002 Iron Metabolism Disease 57 0.059
314
PHR003 Pharyngitis 57 0.059
315
P INF037 Inflammatory Bowel Disease 54 0.059
316
RTN003 Retinal Ischemia 50 0.059
317
c THR090 Thrombocythemia 1 49 0.059
318
INT078 Intracranial Thrombosis 49 0.059
319
INT010 Intracranial Embolism 48 0.059
320
NSS002 Neisseria Meningitidis Infection 47 0.059
321
RTN020 Retinal Vascular Disease 46 0.059
322
MNN020 Meningococcal Infection 46 0.059
323
BNM001 Bone Marrow Cancer 43 0.059
324
MCR011 Microinvasive Gastric Cancer 43 0.059
325
TRP009 Triple X Syndrome 42 0.059
326
DRG024 Drug Allergy 42 0.059
327
CRT004 Carotid Artery Thrombosis 38 0.059
328
INT040 Intrinsic Asthma 34 0.059
329
IMM167 Immune Deficiency Disease 78 0.055
330
SCK003 Sickle Cell Anemia 74 0.055
331
P OST002 Osteoporosis 74 0.055
332
P CNR004 Cone-Rod Dystrophy 2 73 0.055
333
ANX010 Anxiety 73 0.055
334
P HRP006 Herpes Simplex 65 0.055
335
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 63 0.055
336
P PSR002 Psoriasis 62 0.055
337
MDD011 Mood Disorder 62 0.055
338
DRM006 Dermatitis 61 0.055
339
HRP004 Herpes Zoster 60 0.055
340
CNS004 Constipation 58 0.055
341
P GLM007 Glomerulonephritis 57 0.055
342
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.055
343
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.055
344
HLL004 Hellp Syndrome 54 0.055
345
P RTN022 Retinal Vein Occlusion 53 0.055
346
PST011 Pustulosis of Palm and Sole 52 0.055
347
c PRM012 Primary Polycythemia 50 0.055
348
DYS073 Dysphagia 50 0.055
349
DBT008 Diabetic Angiopathy 44 0.055
350
c PRM038 Primary Agammaglobulinemia 44 0.055
351
PST053 Postherpetic Neuralgia 40 0.055
352
ENT001 Enterocele 39 0.055
353
NRL016 Neural Tube Defects 82 0.052
354
CRH001 Crohn's Disease 74 0.052
355
SVR004 Severe Combined Immunodeficiency 73 0.052
356
ULC004 Ulcerative Colitis 73 0.052
357
c SPN225 Spondyloarthropathy 1 73 0.052
358
LYM133 Lymphoma, Hodgkin, Classic 69 0.052
359
P LKM002 Leukemia 68 0.052
360
BRN024 Bronchitis 68 0.052
361
OST159 Osteogenic Sarcoma 66 0.052
362
P NSP012 Nasopharyngeal Carcinoma 66 0.052
363
P HYD006 Hydrocephalus 66 0.052
364
P CNJ013 Conjunctivitis 65 0.052
365
OVR029 Ovarian Hyperstimulation Syndrome 64 0.052
366
NTR005 Nutritional Deficiency Disease 62 0.052
367
VRL011 Viral Infectious Disease 61 0.052
368
NRL005 Neurilemmoma 60 0.052
369
c ACT027 Acute Pancreatitis 60 0.052
370
VRC005 Varicose Veins 60 0.052
371
P THL005 Thalassemia 60 0.052
372
P MYC008 Myocarditis 59 0.052
373
CHL014 Cholera 59 0.052
374
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.052
375
GNG013 Gingivitis 59 0.052
376
TNS005 Tonsillitis 57 0.052
377
P FBR017 Fibrosarcoma 56 0.052
378
HMT008 Hematuria, Benign Familial 56 0.052
379
ACS001 Acoustic Neuroma 56 0.052
380
GST050 Gastrointestinal System Disease 56 0.052
381
c FML035 Familial Hyperlipidemia 55 0.052
382
GLC003 Glucose Intolerance 54 0.052
383
IMP005 Impotence 52 0.052
384
LNG031 Lung Benign Neoplasm 51 0.052
385
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.052
386
ECT026 Ectopic Pregnancy 50 0.052
387
HRT011 Heart Septal Defect 50 0.052
388
DDN006 Duodenitis 49 0.052
389
WTH001 Withdrawal Disorder 48 0.052
390
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.052
391
AGR002 Agoraphobia 45 0.052
392
GNG003 Gingival Recession 44 0.052
393
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.052
394
MMM006 Mammographic Density 41 0.052
396
WBR001 Weber Syndrome 35 0.052
397
P CRN133 Coronary Artery Disease, Autosomal Dominant, 1 32 0.052
398
P LKM071 Leukemia, Chronic Lymphocytic 79 0.048
399
P LNG064 Lung Cancer Susceptibility 3 78 0.048
400
P SCH015 Schizophrenia 74 0.048
401
P NRB001 Neuroblastoma 72 0.048
402
GST040 Gastric Adenocarcinoma 70 0.048
403
P OCL013 Oculodentodigital Dysplasia 69 0.048
404
SRC014 Sarcoma 65 0.048
405
P HML002 Hemolytic Anemia 63 0.048
406
P ENC018 Encephalopathy 61 0.048
407
P VNT002 Ventricular Septal Defect 60 0.048
408
GST045 Gastroenteritis 59 0.048
409
BCT022 Bacterial Infectious Disease 56 0.048
410
SFT003 Soft Tissue Sarcoma 56 0.048
411
MCL006 Macular Retinal Edema 55 0.048
412
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.048
413
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.048
414
HYP060 Hyperinsulinism 54 0.048
415
HRT012 Heart Valve Disease 53 0.048
416
HYP014 Hyperuricemia 52 0.048
417
HYP781 Hypoascorbemia 51 0.048
418
STM007 Stomatitis 50 0.048
419
PRT018 Portal Vein Thrombosis 50 0.048
420
P ART018 Aortic Valve Insufficiency 49 0.048
421
SYN036 Syncope 45 0.048
422
IMM064 Immunodeficiency, Common Variable, 10 44 0.048
423
CRB008 Cerebral Atherosclerosis 44 0.048
424
CLN044 Colon Adenoma 44 0.048
425
IDP033 Idiopathic Edema 44 0.048
426
P MJR007 Major Affective Disorder 1 43 0.048
427
BLR013 Biliary Tract Cancer 42 0.048
428
PPT002 Peptic Ulcer Perforation 36 0.048
429
AMR003 Amaurosis Fugax 34 0.048
431
CHL079 Children's Interstitial Lung Disease 26 0.048
432
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.044
433
c HPT073 Hepatitis C Virus 72 0.044
434
P EPL164 Epilepsy 71 0.044
435
P HYP086 Hypothyroidism 69 0.044
436
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.044
437
P LKM062 Leukemia, Acute Lymphoblastic 69 0.044
438
P LYM118 Lymphoma 68 0.044
439
CNN005 Connective Tissue Disease 68 0.044
440
PSY004 Psychotic Disorder 67 0.044
441
KRT019 Keratitis, Hereditary 65 0.044
442
PRT037 Pertussis 65 0.044
443
MSC007 Muscle Hypertrophy 64 0.044
444
P TRC086 Trichohepatoenteric Syndrome 1 62 0.044
445
CHL068 Cholestasis 61 0.044
446
PSR001 Psoriatic Arthritis 61 0.044
447
P NPH012 Nephrotic Syndrome 60 0.044
448
ING001 Inguinal Hernia 60 0.044
449
IRN001 Iron Deficiency Anemia 59 0.044
450
INC002 Inclusion Body Myositis 58 0.044
451
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.044
452
DSS008 Disease of Mental Health 58 0.044
453
P MYS005 Myositis 56 0.044
454
P PLY011 Polycystic Ovary Syndrome 56 0.044
455
SCH003 Schizophreniform Disorder 56 0.044
456
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.044
457
P HYP076 Hyperthyroidism 55 0.044
458
P VNS003 Venous Insufficiency 55 0.044
459
MNN032 Meningococcal Meningitis 54 0.044
460
TND005 Tendinitis 54 0.044
461
AMN001 Amenorrhea 54 0.044
462
HMC014 Homocysteinemia 53 0.044
463
SPN035 Spindle Cell Sarcoma 53 0.044
464
NRT001 Neurotic Disorder 53 0.044
465
P PNC025 Panic Disorder 53 0.044
466
P INT068 Intestinal Disease 53 0.044
467
P RTN018 Retinal Disease 53 0.044
468
c VRL010 Viral Hepatitis 52 0.044
469
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.044
470
P MGR003 Migraine with Aura 52 0.044
471
P CHL066 Cholangitis 51 0.044
472
ACT017 Acute Chest Syndrome 51 0.044
473
P AGG001 Aggressive Periodontitis 50 0.044
474
MTB004 Metabolic Acidosis 50 0.044
475
LFT001 Left Bundle Branch Hemiblock 49 0.044
476
P MGR001 Migraine Without Aura 49 0.044
477
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.044
478
SPL018 Splenomegaly 48 0.044
479
HPR003 Heparin-Induced Thrombocytopenia 48 0.044
480
P RTN014 Retinal Artery Occlusion 47 0.044
481
MYC005 Myocardial Stunning 46 0.044
482
P HMR005 Hemorrhoid 46 0.044
483
ASP026 Asplenia, Isolated Congenital 44 0.044
484
SBC016 Subacute Delirium 44 0.044
485
c PCH010 Pachyonychia Congenita 3 44 0.044
486
49X006 49, Xxxxy Syndrome 41 0.044
487
P MLG074 Malignant Mesenchymoma 40 0.044
488
BRN026 Branch Retinal Artery Occlusion 40 0.044
489
DBT007 Diabetic Cataract 38 0.044
490
c OVR114 Ovarian Cancer 1 38 0.044
491
c MJR008 Major Affective Disorder 2 35 0.044
492
c MJR023 Major Affective Disorder 7 33 0.044
493
c MJR003 Major Affective Disorder 6 33 0.044
494
c MJR006 Major Affective Disorder 5 33 0.044
495
SNG003 Single Ventricular Heart 30 0.044
496
FNT004 Fainting 30 0.044
497
RSP007 Respiratory Distress Syndrome, Infant 30 0.044
498
c MJR004 Major Affective Disorder 4 28 0.044
499
P OVR096 Overlap Myositis 27 0.044
500
ACT094 Acute Articular Rheumatism 26 0.044
501
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.044
502
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.039
503
CYS001 Cystic Fibrosis 81 0.039
504
P GLM040 Glioma Susceptibility 1 81 0.039
505
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.039
506
c TBR026 Tuberous Sclerosis 2 72 0.039
507
P MYP004 Myopathy 70 0.039
508
P TBR001 Tuberous Sclerosis 70 0.039
509
c BSL007 Basal Cell Carcinoma 68 0.039
510
PNC129 Pancreatic Adenocarcinoma 68 0.039
511
FCT007 Factor Vii Deficiency 67 0.039
512
c FML346 Familial Adenomatous Polyposis 1 66 0.039
513
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 64 0.039
514
c DPH024 Diaphragmatic Hernia, Congenital 63 0.039
515
c HPT001 Hepatitis C 62 0.039
516
CHR001 Churg-Strauss Syndrome 61 0.039
517
SPN186 Spinal Cord Injury 60 0.039
518
c LPM012 Lipomatosis, Multiple 60 0.039
519
CRD223 Cardiac Arrhythmia 60 0.039
520
P ATR010 Atrial Heart Septal Defect 60 0.039
521
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.039
522
P PTN014 Patent Ductus Arteriosus 1 60 0.039
523
STT001 Status Epilepticus 60 0.039
524
c HPT016 Hepatitis B 59 0.039
525
CHL123 Chlamydia 59 0.039
526
P BRS044 Breast Adenocarcinoma 59 0.039
527
P CYS018 Cystitis 59 0.039
528
RNL024 Renal Glucosuria 58 0.039
529
c ACT073 Acute Leukemia 58 0.039
530
P ALC033 Alcohol Use Disorder 58 0.039
531
P ESP035 Esophagitis, Eosinophilic, 1 57 0.039
532
AYM001 Ayme-Gripp Syndrome 57 0.039
533
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.039
534
END040 Endogenous Depression 55 0.039
535
SYN007 Synovitis 54 0.039
536
PRT082 Preterm Premature Rupture of the Membranes 54 0.039
537
GST037 Gastroparesis 54 0.039
538
GST009 Gastroschisis 53 0.039
539
KRT006 Keratoconjunctivitis 53 0.039
540
BRN038 Bronchial Disease 53 0.039
541
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.039
542
CHR073 Choreatic Disease 52 0.039
543
MTP025 Metaphyseal Chondrodysplasia, Schmid Type 52 0.039
544
SPN051 Spondylitis 51 0.039
545
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.039
546
CLR109 Colorectal Adenocarcinoma 51 0.039
547
NRM004 Neuroma 51 0.039
548
P PRC012 Pericardial Effusion 51 0.039
549
P PST095 Post-Thrombotic Syndrome 51 0.039
550
BHR001 Behr Syndrome 51 0.039
551
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.039
552
SCB001 Scabies 50 0.039
553
PLR008 Pleurisy 50 0.039
554
P MTR003 Mitral Valve Stenosis 50 0.039
555
STT002 Status Asthmaticus 50 0.039
556
NTR046 Neutrophil Migration 50 0.039
557
P ATR005 Atrophic Gastritis 50 0.039
558
P OPN001 Open-Angle Glaucoma 49 0.039
559
URM002 Uremia 49 0.039
560
NRL018 Neural Tube Defects, Folate-Sensitive 48 0.039
561
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.039
562
HMP001 Hemopericardium 48 0.039
563
c MTR002 Mitral Valve Insufficiency 48 0.039
564
CLN019 Colonic Disease 47 0.039
565
VRN004 Vernal Keratoconjunctivitis 47 0.039
566
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.039
567
c DRR009 Diarrhea 6 46 0.039
568
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.039
569
INT253 Intestinal Benign Neoplasm 45 0.039
570
IMM136 Immune System Disease 45 0.039
571
ESP027 Esophagus Squamous Cell Carcinoma 45 0.039
572
CRT015 Carotid Artery Occlusion 45 0.039
573
TND004 Tendinopathy 43 0.039
574
c CNT028 Central Retinal Artery Occlusion 43 0.039
575
THR035 Thrombasthenia 40 0.039
576
ANG049 Angioedema Induced by Ace Inhibitors 40 0.039
577
CRN020 Coronary Restenosis 39 0.039
578
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.039
579
c CHR682 Chronic Bilirubin Encephalopathy 39 0.039
580
ANG065 Angioma, Tufted 38 0.039
581
ATM052 Autoimmune Disease 1 37 0.039
582
THR123 Thrombotic Microangiopathy 36 0.039
583
ABD010 Abdominal Wall Defect 36 0.039
584
PLC002 Plica Syndrome 36 0.039
585
INT003 Intracranial Hypotension 35 0.039
586
c MYC058 Myocardial Infarction 2 34 0.039
587
DDN004 Duodenogastric Reflux 33 0.039
588
INF009 Inflammatory Spondylopathy 31 0.039
589
RNL001 Renal Artery Obstruction 31 0.039
590
c CRN214 Coronary Heart Disease 5 24 0.039
591
INT074 Intracranial Arteriosclerosis 23 0.039
592
P ATX030 Ataxia-Telangiectasia 82 0.034
593
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.034
594
c NRF023 Neurofibromatosis, Type Ii 80 0.034
595
P PRK057 Parkinson Disease, Late-Onset 78 0.034
596
c TBR025 Tuberous Sclerosis 1 77 0.034
597
BRN028 Brain Cancer 74 0.034
598
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.034
599
MLT157 Multiple System Atrophy 1 70 0.034
600
P HYP061 Hypertrophic Cardiomyopathy 70 0.034
601
CRB037 Cerebral Palsy 69 0.034
602
P SLP006 Sleep Apnea 69 0.034
603
P LPR021 Leprosy 3 69 0.034
604
LYM007 Lymphangioleiomyomatosis 69 0.034
605
P SYS005 Systemic Scleroderma 68 0.034
606
P INF038 Influenza 68 0.034
607
FLL027 Fallopian Tube Carcinoma 67 0.034
608
P ART005 Arteriovenous Malformation 65 0.034
609
APN008 Apnea, Obstructive Sleep 64 0.034
610
NRF007 Neurofibroma 64 0.034
611
CLF027 Cleft Palate, Isolated 64 0.034
612
P ANR048 Aniridia 1 63 0.034
613
TYP007 Typhoid Fever 63 0.034
614
c ACT068 Acute Cystitis 63 0.034
615
ANR007 Anorexia Nervosa 63 0.034
616
c ALP101 Alpha-Thalassemia 62 0.034
617
MSS001 Masa Syndrome 62 0.034
618
OST003 Osteonecrosis 61 0.034
619
ARG002 Argininosuccinic Aciduria 61 0.034
620
RTN017 Retinal Detachment 61 0.034
621
HPT019 Hepatic Encephalopathy 60 0.034
622
ACN002 Acanthosis Nigricans 60 0.034
623
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.034
624
ANT009 Antithrombin Iii Deficiency 59 0.034
625
SPP011 Suppression of Tumorigenicity 12 59 0.034
626
P BND020 Bone Disease 59 0.034
627
P BRN022 Bronchiectasis 59 0.034
628
c DNG003 Dengue Disease 59 0.034
629
PRT058 Pure Autonomic Failure 59 0.034
630
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.034
631
CNT047 Contact Dermatitis 58 0.034
632
LYM027 Lymphopenia 58 0.034
633
P CND004 Candidiasis 58 0.034
634
PLS011 Plasmacytoma 56 0.034
635
c PRX059 Peroxisome Biogenesis Disorder 1a 56 0.034
636
ALL010 Allergic Contact Dermatitis 56 0.034
637
P NRF002 Neurofibromatosis 56 0.034
638
MCS002 Mucositis 56 0.034
639
P HYP838 Hyperlipidemia, Familial Combined, 3 56 0.034
640
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.034
641
ATR057 Atrioventricular Block 55 0.034
642
P SCK002 Sick Sinus Syndrome 55 0.034
643
P MYP006 Myopia 55 0.034
644
THR013 Thoracic Outlet Syndrome 54 0.034
645
P LTR001 Lateral Sclerosis 54 0.034
646
HMS001 Hemosiderosis 54 0.034
647
SNS003 Sensory Peripheral Neuropathy 54 0.034
648
NNL006 Non-Alcoholic Steatohepatitis 54 0.034
649
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.034
650
MMM001 Mammary Paget's Disease 53 0.034
651
FRZ001 Frozen Shoulder 53 0.034
652
PLS016 Plasma Cell Leukemia 53 0.034
653
P HML001 Hemolytic-Uremic Syndrome 53 0.034
654
CLF001 Cleft Lip 53 0.034
655
DNT012 Dental Caries 53 0.034
656
c HYP740 Hyperlipoproteinemia, Type V 53 0.034
657
c PSR017 Psoriasis 2 53 0.034
658
EXP004 Exophthalmos 52 0.034
659
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.034
660
c PSR023 Psoriasis 1 52 0.034
661
TLN003 Telangiectasis 52 0.034
662
LMY002 Leiomyoma 52 0.034
663
OLG003 Oligohydramnios 51 0.034
664
P SPP010 Suppressor of Tumorigenicity 3 51 0.034
665
FCT001 Factor Viii Deficiency 51 0.034
666
P MND003 Mandibuloacral Dysplasia with Type a Lipodystrophy 51 0.034
667
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 51 0.034
668
P MMB011 Membranous Nephropathy 50 0.034
669
P ESN008 Eosinophilic Pneumonia 50 0.034
670
CHR515 Chronic Atrial and Intestinal Dysrhythmia 50 0.034
671
c INF145 Infantile Liver Failure Syndrome 1 50 0.034
672
P TMP001 Temporal Lobe Epilepsy 50 0.034
673
SYS003 Systolic Heart Failure 49 0.034
674
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.034
675
c CHR431 Chronic Venous Insufficiency 49 0.034
676
BRS064 Bursitis 48 0.034
677
CHL147 Chlamydia Pneumonia 48 0.034
678
ART004 Aortic Atherosclerosis 47 0.034
679
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 47 0.034
680
c PSR032 Psoriasis 11 47 0.034
681
KHN001 Kuhnt-Junius Degeneration 47 0.034
682
c INH020 Inherited Metabolic Disorder 47 0.034
683
RYN005 Raynaud Phenomenon 47 0.034
684
P BLD051 Blood Coagulation Disease 46 0.034
685
GNR003 Generalized Atherosclerosis 46 0.034
686
KRT013 Keratolytic Winter Erythema 46 0.034
687
RCT017 Rectal Disease 46 0.034
688
CRN019 Coronary Artery Vasospasm 46 0.034
689
P HRN001 Horner's Syndrome 45 0.034
690
c EST002 Estrogen-Receptor Negative Breast Cancer 45 0.034
691
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.034
692
HPT004 Hepatic Coma 45 0.034
693
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.034
694
HMR002 Hemarthrosis 45 0.034
695
ANS012 Anus Disease 45 0.034
696
GRN017 Granulocytopenia 44 0.034
697
HRT015 Heritable Pulmonary Arterial Hypertension 44 0.034
698
PRT014 Protein S Deficiency 44 0.034
699
HPT082 Hepatic Adenomas, Familial 44 0.034
700
KPS002 Kaposiform Hemangioendothelioma 43 0.034
701
c PSR028 Psoriasis 7 42 0.034
702
c AVS006 Avascular Necrosis of Femoral Head, Primary, 1 42 0.034
703
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.034
704
c PSR018 Psoriasis 13 41 0.034
705
RDN001 Reading Disorder 40 0.034
706
SPR126 Superior Semicircular Canal Dehiscence 40 0.034
707
EXT006 Extrahepatic Cholestasis 39 0.034
708
c HMG029 Hemoglobin Se Disease 39 0.034
709
ADP007 Adie Pupil 39 0.034
710
ALL014 Allergic Encephalomyelitis 38 0.034
711
NCR002 Necrobiosis Lipoidica 38 0.034
712
OPT010 Optic Papillitis 38 0.034
713
MDD003 Middle Cerebral Artery Infarction 36 0.034
714
BRR002 Barrett's Adenocarcinoma 36 0.034
715
PSD088 Pseudobulbar Affect 36 0.034
716
BRK012 Broken Heart Syndrome 35 0.034
717
VRN001 Vernal Conjunctivitis 35 0.034
718
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.034
719
ATX010 Ataxia Neuropathy Spectrum 34 0.034
720
DDN009 Duodenal Obstruction 34 0.034
721
HNS001 Hansen's Disease 34 0.034
722
P ANT001 Anterolateral Myocardial Infarction 34 0.034
723
HMN016 Hemangioendothelioma 34 0.034
724
CRT008 Carotid Artery Dissection 33 0.034
725
ACT064 Acute Necrotizing Encephalitis 33 0.034
726
P VSC018 Visceral Steatosis 33 0.034
727
MTP028 Metaphyseal Dysplasia, Spahr Type 32 0.034
728
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.034
729
PLT031 Platelet Membrane Fluidity 29 0.034
730
c HYP839 Hyperlipidemia, Familial Combined, 1 29 0.034
731
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.034
732
HNM002 Hinman Syndrome 27 0.034
733
MYT019 May-Thurner Syndrome 27 0.034
734
CHR669 Chromosome 2p16.3 Deletion Syndrome 26 0.034
735
NRF026 Neurofibromatosis, Type Iv, of Riccardi 26 0.034
736
FTL073 Fetal Anticonvulsant Syndrome 26 0.034
737
ATR055 Atrial Septal Aneurysm 25 0.034
738
HRP008 Herpes Simiae 25 0.034
739
ALL012 Allergic Angiitis 24 0.034
740
MNS002 Mini Stroke 19 0.034
741
BLD137 Blood Group--Ahonen 16 0.034
742
c LKM061 Leukemia, Acute Myeloid 84 0.028
743
c DLT002 Dilated Cardiomyopathy 79 0.028
744
LPT014 Leptin Deficiency or Dysfunction 74 0.028
745
c MNN043 Meningioma, Familial 74 0.028
746
P AMY004 Amyloidosis 70 0.028
747
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 0.028
748
P MLN066 Melanoma, Cutaneous Malignant 1 70 0.028
749
PLM001 Pulmonary Tuberculosis 69 0.028
750
P ANG001 Angelman Syndrome 69 0.028
751
P TMP003 Temporal Arteritis 68 0.028
752
P FLL037 Follicular Lymphoma 67 0.028
753
c HMP029 Hemophilia a 67 0.028
754
ALC007 Alcohol Dependence 66 0.028
755
GLN010 Glanzmann Thrombasthenia 66 0.028
756
ART001 Arterial Tortuosity Syndrome 66 0.028
757
AND002 Androgen Insensitivity Syndrome 66 0.028
758
P NRV007 Nervous System Disease 66 0.028
759
P PLM036 Pulmonary Fibrosis 65 0.028
760
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.028
761
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 65 0.028
762
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.028
763
IRR002 Irritable Bowel Syndrome 65 0.028
764
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.028
765
P THY023 Thymoma 65 0.028
766
P MST009 Mastocytosis 64 0.028
767
ART002 Arts Syndrome 64 0.028
768
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.028
769
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.028
770
c MLG084 Malignant Fibrous Histiocytoma 63 0.028
771
SKN016 Skin Disease 63 0.028
772
P SHR029 Short Syndrome 63 0.028
773
P HRD008 Hereditary Hemorrhagic Telangiectasia 63 0.028
774
c SYS004 Systemic Mastocytosis 63 0.028
775
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 63 0.028
776
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.028
777
HMT002 Hematologic Cancer 62 0.028
778
P ACR001 Aicardi-Goutieres Syndrome 62 0.028
779
MNN042 Meningioma, Radiation-Induced 62 0.028
781
c SCL052 Scleroderma, Familial Progressive 61 0.028
782
ALV005 Alveolar Soft Part Sarcoma 61 0.028
783
APP008 Appendicitis 61 0.028
784
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.028
785
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.028
786
c HRD002 Hereditary Angioedema 60 0.028
787
P BRN019 Bernard-Soulier Syndrome 60 0.028
788
P AXN002 Axenfeld-Rieger Syndrome 59 0.028
789
THY029 Thyroid Carcinoma 59 0.028
790
P SYP003 Syphilis 58 0.028
791
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.028
792
ERY029 Erythermalgia, Primary 58 0.028
793
P PGT001 Paget's Disease of Bone 58 0.028
794
CMP010 Complex Regional Pain Syndrome 58 0.028
795
c PTT056 Pituitary Adenoma 1, Multiple Types 58 0.028
796
P EHL001 Ehlers-Danlos Syndrome 58 0.028
797
BRG013 Buerger Disease 58 0.028
798
P PRP019 Peripheral Nervous System Disease 58 0.028
799
P GLL018 Gallbladder Cancer 57 0.028
800
P UVT001 Uveitis 57 0.028
801
CHL067 Cholecystitis 57 0.028
802
P MYM013 Moyamoya Disease 1 57 0.028
803
P PRN023 Prion Disease 57 0.028
804
c MST023 Mesothelioma, Malignant 57 0.028
805
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.028
806
CYT008 Cytomegalovirus Infection 57 0.028
807
TRN018 Transitional Cell Carcinoma 56 0.028
808
ERY051 Erythroleukemia, Familial 56 0.028
809
GNR004 Generalized Anxiety Disorder 56 0.028
810
HMG005 Hemoglobinopathy 56 0.028
811
c GRV008 Graves Disease 1 56 0.028
812
BRN004 Brain Edema 56 0.028
813
NRN004 Neuroendocrine Tumor 55 0.028
814
c PRG126 Progressive Familial Heart Block 55 0.028
815
ZLL002 Zollinger-Ellison Syndrome 55 0.028
816
MMB001 Membranoproliferative Glomerulonephritis 55 0.028
817
DFF005 Diffuse Large B-Cell Lymphoma 55 0.028
818
NPH009 Nephrolithiasis 55 0.028
819
P PLM034 Pulmonary Emphysema 55 0.028
820
CHR100 Chronic Ulcer of Skin 55 0.028
821
P ALP106 Alport Syndrome 1, X-Linked 55 0.028
822
FCT004 Factor Xii Deficiency 55 0.028
823
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.028
824
P ALP008 Alopecia 54 0.028
825
PPL022 Papilloma 54 0.028
826
PRS045 Prostatic Hypertrophy 53 0.028
827
P INS002 in Situ Carcinoma 53 0.028
828
P HYP083 Hypopituitarism 53 0.028
829
HYP063 Hypersplenism 53 0.028
830
INT075 Intracranial Hypertension 53 0.028
831
IRD001 Iridocyclitis 53 0.028
832
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 53 0.028
833
PRP016 Paraplegia 52 0.028
834
P SML001 Small Cell Carcinoma 52 0.028
835
c ACR116 Aicardi-Goutieres Syndrome 1 52 0.028
836
c THY107 Thymoma, Familial 52 0.028
837
P THY032 Thyroiditis 52 0.028
838
ART074 Aortic Dissection 52 0.028
839
PRS021 Prostatic Adenoma 51 0.028
840
ILS001 Ileus 51 0.028
841
THR016 Thrombophlebitis 51 0.028
842
P HYP040 Hypospadias 51 0.028
843
SKN013 Skin Benign Neoplasm 51 0.028
844
HYP081 Hypolipoproteinemia 51 0.028
845
RDC002 Radiculopathy 50 0.028
846
SPN021 Spinal Meningioma 50 0.028
847
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.028
848
c DYS119 Dystonia 9 50 0.028
849
P MYT002 Myotonic Dystrophy 49 0.028
850
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.028
851
PRS129 Prostatic Hyperplasia, Benign 49 0.028
852
CHL004 Cholelithiasis 49 0.028
853
c ACT150 Acute Adrenal Insufficiency 48 0.028
854
INT067 Interstitial Nephritis 48 0.028
855
IGG001 Iga Glomerulonephritis 48 0.028
856
PYL006 Pyloric Stenosis 48 0.028
857
P UTR058 Uterine Anomalies 47 0.028
858
PRD004 Prediabetes Syndrome 47 0.028
859
P RNL015 Renal Hypertension 47 0.028
860
RNL077 Renal Fibrosis 47 0.028
861
P CLL015 Collagen Disease 47 0.028
862
STR089 Storage Pool Platelet Disease 47 0.028
863
KRT002 Keratomalacia 47 0.028
864
CHR074 Choriocarcinoma 47 0.028
865
P BNG032 Benign Mesothelioma 46 0.028
866
c MLG068 Malignant Glioma 46 0.028
867
NWC001 Newcastle Disease 45 0.028
868
P OCY003 Oocyte Maturation Defect 1 45 0.028
869
ACT003 Acute Kidney Tubular Necrosis 45 0.028
870
CLL014 Cll/sll 45 0.028
871
SPS057 Spasticity 45 0.028
872
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.028
873
c DRM054 Dermatitis, Atopic, 2 44 0.028
874
RTN021 Retinal Vascular Occlusion 44 0.028
875
RFR003 Refractive Error 43 0.028
876
MGS001 Megaesophagus 43 0.028
877
BNS003 Binswanger's Disease 42 0.028
878
P CRN035 Cranial Nerve Palsy 42 0.028
879
SNL007 Senile Cataract 42 0.028
880
FBR019 Fibromatosis 41 0.028
881
P RRH023 Rare Hereditary Hemochromatosis 41 0.028
882
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 41 0.028
883
SCR001 Secretory Meningioma 41 0.028
884
CNN010 Connective Tissue Benign Neoplasm 40 0.028
885
HYP540 Hypertension, Diastolic 40 0.028
886
ART008 Arteriosclerosis Obliterans 40 0.028
887
UTR043 Uterine Sarcoma 39 0.028
888
C1N001 C1 Inhibitor Deficiency 39 0.028
889
LKP003 Leukoplakia 39 0.028
890
ORL012 Oral Leukoplakia 39 0.028
891
HYP344 Hyperthyroidism, Familial Gestational 39 0.028
892
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.028
893
TRC005 Tracheal Stenosis 38 0.028
894
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.028
895
NRW001 Norwegian Scabies 37 0.028
896
c ATM104 Autoimmune Vasculitis 37 0.028
897
FST001 Foster-Kennedy Syndrome 36 0.028
898
HRW001 Hair Whorl 36 0.028
899
LVD003 Livedoid Vasculitis 36 0.028
900
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.028
901
LCH001 Leech Infestation 35 0.028
902
c ATM022 Autoimmune Myocarditis 35 0.028
903
END072 Endotheliitis 35 0.028
904
MLG141 Malignant Atrophic Papulosis 35 0.028
905
PLT015 Platelet Aggregation, Spontaneous 34 0.028
906
c SCN069 Secondary Hemophagocytic Lymphohistiocytosis 33 0.028
907
RTN004 Retinal Microaneurysm 33 0.028
908
ALR002 Al-Raqad Syndrome 33 0.028
909
AMN014 Aminopterin Syndrome Sine Aminopterin 33 0.028
910
SBC014 Subclavian Steal Syndrome 32 0.028
911
CYT004 Cytomegalic Inclusion Disease 31 0.028
912
TTH007 Tooth Erosion 31 0.028
913
GST029 Gastric Cardia Adenocarcinoma 31 0.028
915
PRC051 Paracetamol Poisoning 30 0.028
916
UND007 Undifferentiated Connective Tissue Disease 29 0.028
917
STR033 Storm Syndrome 26 0.028
918
BLD163 Blood Group, Dombrock System 24 0.028
919
ORL006 Oral Mucosa Leukoplakia 23 0.028
920
MSC026 Muscular Dystrophy White Matter Spongiosis 15 0.028
921
APC006 Apc-Associated Polyposis Conditions 12 0.028
922
CNN003 Conn's Syndrome 79 0.020
923
INS024 Insulin-Like Growth Factor I 79 0.020
924
GST019 Gastrointestinal Stromal Tumor 78 0.020
925
ADR007 Adrenoleukodystrophy 75 0.020
926
c BTT014 Beta-Thalassemia 74 0.020
927
BSL036 Basal Cell Nevus Syndrome 73 0.020
928
P FML018 Familial Mediterranean Fever 73 0.020
929
P RTN024 Retinoblastoma 73 0.020
930
P HNT016 Huntington Disease 72 0.020
931
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.020
932
P GRF003 Graft-Versus-Host Disease 72 0.020
933
OTT002 Otitis Media 72 0.020
934
c LKM063 Leukemia, Chronic Myeloid 72 0.020
935
P PHC003 Pheochromocytoma 71 0.020
936
ACR007 Acromegaly 71 0.020
937
ADN011 Adenoid Cystic Carcinoma 70 0.020
938
P TTR001 Tetralogy of Fallot 70 0.020
939
P ASP006 Aspergillosis 69 0.020
940
P PRM011 Primary Ciliary Dyskinesia 69 0.020
941
c MYT021 Myotonic Dystrophy 1 69 0.020
942
P HML033 Hemolytic Uremic Syndrome, Atypical 1 68 0.020
943
c HMP004 Hemophilia B 68 0.020
944
P CRB048 Cerebral Cavernous Malformations 67 0.020
945
c INF071 Inflammatory Bowel Disease 1 67 0.020
946
P BLD062 Bile Duct Cancer 67 0.020
947
P CLC063 Celiac Disease 1 66 0.020
948
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.020
949
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.020
950
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 65 0.020
951
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 65 0.020
952
P PRS038 Personality Disorder 65 0.020
953
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.020
954
P HRM001 Hermansky-Pudlak Syndrome 64 0.020
955
P CMP005 Campomelic Dysplasia 64 0.020
956
BRC012 Brucellosis 64 0.020
957
DGR001 Digeorge Syndrome 64 0.020
958
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 64 0.020
959
P RHB003 Rhabdomyosarcoma 63 0.020
960
P HYP055 Hypoplastic Left Heart Syndrome 63 0.020
961
END041 Endometrial Adenocarcinoma 63 0.020
962
P MVM001 Movement Disease 63 0.020
963
P LMY004 Leiomyosarcoma 63 0.020
964
P END044 Endometriosis 63 0.020
965
BDD001 Budd-Chiari Syndrome 63 0.020
966
c GLC092 Glaucoma, Primary Open Angle 62 0.020
967
P PLY014 Polycystic Kidney Disease 62 0.020
968
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.020
969
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.020
970
BLL006 Bullous Pemphigoid 62 0.020
971
P ART023 Arthropathy 62 0.020
972
CRN239 Carnitine Deficiency, Systemic Primary 62 0.020
973
HSH003 Hashimoto Thyroiditis 62 0.020
974
CRC021 Carcinosarcoma 62 0.020
975
BLD131 Bladder Urothelial Carcinoma 62 0.020
976
MSL001 Measles 62 0.020
977
MCK005 Mckusick-Kaufman Syndrome 61 0.020
978
c THR082 Thrombophilia Due to Activated Protein C Resistance 61 0.020
979
DCB001 Decubitus Ulcer 61 0.020
980
P MYL006 Myeloid Leukemia 60 0.020
981
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.020
982
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 60 0.020
983
c JVN061 Juvenile Arthritis 60 0.020
984
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.020
985
ORL011 Oral Cancer 60 0.020
986
LNG073 Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.020
987
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.020
988
ETN001 Eating Disorder 60 0.020
989
P HRD011 Hereditary Spherocytosis 60 0.020
990
FCT002 Factor Xi Deficiency 60 0.020
991
ORN008 Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to 59 0.020
992
P MCR010 Microcephaly 59 0.020
993
PRN019 Perinatal Necrotizing Enterocolitis 59 0.020
994
GRY002 Gray Platelet Syndrome 59 0.020
995
P PLY006 Polydactyly 59 0.020
996
P ANP001 Anaplastic Large Cell Lymphoma 58 0.020
997
ALK013 Alkaptonuria 58 0.020
998
MTC027 Mitochondrial Trifunctional Protein Deficiency 58 0.020
999
BRS051 Breast Disease 58 0.020
1000
P MTR012 Mitral Valve Disease 58 0.020
1001
P BNC003 Bone Cancer 58 0.020
1002
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 58 0.020
1003
EXT034 Extrinsic Allergic Alveolitis 58 0.020
1004
P FNC044 Fanconi Anemia, Complementation Group C 57 0.020
1005
APL002 Aplasia of Lacrimal and Salivary Glands 57 0.020
1006
TTL012 Total Anomalous Pulmonary Venous Return 1 57 0.020
1007
BLM002 Bulimia Nervosa 57 0.020
1008
MCR013 Microphthalmia 57 0.020
1009
c CHL119 Cholangitis, Primary Sclerosing 57 0.020
1010
CHK001 Chikungunya 57 0.020
1011
P SLV026 Salivary Gland Carcinoma 57 0.020
1012
APH002 Aphasia 57 0.020
1013
P FTL001 Fetal Alcohol Syndrome 57 0.020
1014
c ANG068 Angioedema, Hereditary, Type I 57 0.020
1015
BLR008 Bilirubin Metabolic Disorder 57 0.020
1016
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.020
1017
INT303 Intracranial Hypertension, Idiopathic 57 0.020
1018
P CHN012 Chondrosarcoma 56 0.020
1019
P MLT074 Multiple Endocrine Neoplasia 56 0.020
1020
c ACT134 Acute Liver Failure 56 0.020
1021
LMY014 Leiomyoma, Uterine 56 0.020
1022
SPN041 Spinal Cord Disease 56 0.020
1023
ANN002 Anencephaly 56 0.020
1024
EHL052 Ehlers-Danlos Syndrome, Vascular Type 56 0.020
1025
INS023 Insensitivity to Pain, Congenital, with Anhidrosis 56 0.020
1026
CRN295 Carnitine Palmitoyltransferase I Deficiency 56 0.020
1027
FLR001 Filarial Elephantiasis 55 0.020
1028
ORP003 Oropharynx Cancer 55 0.020
1029
P MLN007 Male Infertility 55 0.020
1030
P SBS003 Substance Abuse 55 0.020
1031
FLR002 Filariasis 55 0.020
1032
ESN005 Eosinophilic Gastroenteritis 55 0.020
1033
HNC001 Henoch-Schoenlein Purpura 55 0.020
1034
CLF004 Cleft Lip/palate 54 0.020
1035
P NRM002 Normal Pressure Hydrocephalus 54 0.020
1036
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.020
1037
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 0.020
1038
c THR124 Thrombotic Thrombocytopenic Purpura, Hereditary 54 0.020
1039
P RST001 Restless Legs Syndrome 54 0.020
1040
RLP001 Relapsing Polychondritis 54 0.020
1041
VLC001 Velocardiofacial Syndrome 54 0.020
1042
BRN014 Bronchopneumonia 54 0.020
1043
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.020
1044
DBT010 Diabetic Neuropathy 54 0.020
1045
TRC062 Tricuspid Atresia 54 0.020
1046
LYM040 Lymphoblastic Lymphoma 54 0.020
1047
P TRM003 Tremor 54 0.020
1048
CNT099 Contractural Arachnodactyly, Congenital 53 0.020
1049
P BRC006 Brachydactyly 53 0.020
1050
P MNC007 Monocytic Leukemia 53 0.020
1051
PRP036 Peripheral T-Cell Lymphoma 53 0.020
1052
CRH005 Crohn's Colitis 53 0.020
1053
ACY005 Acyl-Coa Dehydrogenase, Short-Chain, Deficiency of 53 0.020
1054
P RTN016 Retinal Degeneration 53 0.020
1055
P ALL008 Allergic Bronchopulmonary Aspergillosis 53 0.020
1056
MST005 Mastitis 53 0.020
1057
P PTS002 Ptosis 53 0.020
1058
c XNT010 Xanthinuria, Type I 53 0.020
1059
P FBR031 Febrile Seizures 53 0.020
1060
TXC002 Toxic Encephalopathy 53 0.020
1061
c FML008 Familial Retinoblastoma 53 0.020
1062
P ATN002 Autonomic Nervous System Disease 52 0.020
1063
P LRY019 Laryngitis 52 0.020
1064
DMY004 Demyelinating Disease 52 0.020
1065
LYS002 Lysosomal Storage Disease 52 0.020
1066
ACR041 Acromelic Frontonasal Dysostosis 52 0.020
1067
FML037 Female Breast Cancer 52 0.020
1068
P OVR049 Ovarian Disease 52 0.020
1069
c VRL005 Viral Pneumonia 52 0.020
1070
SRS001 Serous Cystadenocarcinoma 52 0.020
1071
c HYP843 Hypoalphalipoproteinemia, Primary, 2 52 0.020
1072
ENT011 Enterocolitis 51 0.020
1073
P LCT001 Lactic Acidosis 51 0.020
1074
ESP002 Esophageal Varix 51 0.020
1075
CLB002 Clubfoot 51 0.020
1076
BLL003 Bell's Palsy 51 0.020
1077
ACH005 Achalasia 51 0.020
1078
P AST007 Astrocytoma 51 0.020
1079
SCH012 Schizoaffective Disorder