Search results for Angiotensin II

1522 hits were found for Angiotensin II

# Family MCID Name MIFTS Score
1
c HYP595 Hypertension, Essential 84 0.639
2
CNG034 Congestive Heart Failure 69 0.559
3
c MCR113 Microvascular Complications of Diabetes 3 52 0.536
4
c MCR120 Microvascular Complications of Diabetes 7 47 0.529
5
c MCR130 Microvascular Complications of Diabetes 6 41 0.529
6
c MCR133 Microvascular Complications of Diabetes 4 41 0.529
7
P KDN018 Kidney Disease 72 0.525
8
P HRT032 Heart Disease 75 0.435
9
c CHR684 Chronic Kidney Disease 70 0.420
10
P NTR004 Neutropenia 63 0.376
11
P VSC007 Vascular Disease 63 0.358
12
END086 End Stage Renal Disease 51 0.357
13
P SRC025 Sarcoidosis 1 70 0.344
14
P LNG032 Lung Cancer 98 0.336
15
P ANG015 Angioedema 57 0.326
16
LPP008 Lipoprotein Quantitative Trait Locus 62 0.326
17
P CRN300 Coronary Heart Disease 1 63 0.322
18
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.321
19
P MYC007 Myocardial Infarction 70 0.316
20
ATH013 Atherosclerosis Susceptibility 65 0.314
21
P DBT009 Diabetes Mellitus 64 0.307
22
c PRC016 Pre-Eclampsia 63 0.307
23
P RNV001 Renovascular Hypertension 48 0.304
24
P BRS047 Breast Cancer 97 0.301
25
ART016 Aortic Aneurysm 69 0.300
26
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.297
27
PRT037 Pertussis 65 0.296
28
c SML038 Small Cell Cancer of the Lung 65 0.294
29
P ADN016 Adenocarcinoma 64 0.281
30
P GLM007 Glomerulonephritis 57 0.280
31
P CLR023 Colorectal Cancer 99 0.274
32
DWN001 Down Syndrome 70 0.274
33
ART140 Arteries, Anomalies of 52 0.273
34
ANR040 Aneurysm 59 0.272
35
c ACT075 Acute Myocardial Infarction 57 0.271
36
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.269
37
CVD001 Covid-19 44 0.269
38
P LYM118 Lymphoma 68 0.268
39
P MCR115 Microvascular Complications of Diabetes 5 66 0.260
40
P CRD246 Cardiovascular System Disease 57 0.260
41
P PNC035 Pancreatic Cancer 84 0.254
42
ISC004 Ischemia 58 0.252
43
c SVR001 Severe Acute Respiratory Syndrome 62 0.246
44
RNL077 Renal Fibrosis 47 0.245
45
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.244
46
LVR012 Liver Cirrhosis 62 0.244
47
P PRS040 Prostate Cancer 97 0.241
48
HYP066 Hyperglycemia 61 0.240
49
P RNL015 Renal Hypertension 47 0.240
50
P ATR011 Atrial Fibrillation 66 0.239
51
48X005 48,xyyy 39 0.237
52
STR067 Stroke, Ischemic 81 0.235
53
c ACT071 Acute Kidney Failure 60 0.235
54
LYM019 Lymphosarcoma 46 0.235
55
P OVR042 Ovarian Cancer 88 0.235
56
P LKM002 Leukemia 68 0.234
57
c PRM038 Primary Agammaglobulinemia 44 0.232
58
c HYP836 Hypercholesterolemia, Familial, 1 73 0.225
59
MSC007 Muscle Hypertrophy 64 0.223
60
P LVR013 Liver Disease 68 0.222
61
P PLM037 Pulmonary Hypertension 67 0.222
62
P NRP001 Neuropathy 56 0.222
63
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.217
64
HYP266 Hypoxia 57 0.212
65
P EXN002 Exanthem 57 0.211
66
P NRB001 Neuroblastoma 72 0.211
67
c ATR087 Atrial Standstill 1 75 0.210
68
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.210
69
LPD008 Lipid Metabolism Disorder 62 0.209
70
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.209
71
ATM095 Autoimmune Disease 62 0.209
72
CRB039 Cerebrovascular Disease 67 0.207
73
SQM006 Squamous Cell Carcinoma 60 0.206
74
GLB015 Glioblastoma Multiforme 75 0.203
75
P MLN008 Melanoma 69 0.202
76
P GST053 Gastric Cancer 83 0.201
77
c RHB024 Rhabdomyosarcoma 2 67 0.201
78
P ALZ034 Alzheimer Disease 88 0.199
79
IGG001 Iga Glomerulonephritis 48 0.199
80
LNG099 Lung Disease 60 0.197
81
P DRR001 Diarrhea 55 0.197
82
P TRN020 Turner Syndrome 67 0.197
83
c DLT002 Dilated Cardiomyopathy 79 0.196
84
LNG031 Lung Benign Neoplasm 51 0.196
85
HYP056 Hypoglycemia 66 0.196
86
P HPT023 Hepatocellular Carcinoma 100 0.196
87
P NPH012 Nephrotic Syndrome 60 0.194
88
CYT002 Cytokine Deficiency 42 0.194
89
P GLM045 Glioma 63 0.194
90
P MYL006 Myeloid Leukemia 60 0.193
91
GLL048 Glial Tumor 45 0.193
92
P PLM036 Pulmonary Fibrosis 65 0.192
93
MYL069 Myeloma, Multiple 85 0.192
94
ALL026 Allergic Hypersensitivity Disease 62 0.190
95
P THR014 Thrombocytopenia 67 0.189
96
LYM133 Lymphoma, Hodgkin, Classic 69 0.189
97
HYP060 Hyperinsulinism 54 0.187
98
ADN018 Adenoma 59 0.186
99
P BCL017 B-Cell Lymphoma 58 0.186
100
P BLD134 Bladder Cancer 79 0.186
101
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.186
102
c DBT099 Diabetes Mellitus, Type I 65 0.184
103
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.181
104
P PRP019 Peripheral Nervous System Disease 58 0.181
105
P KDN017 Kidney Cancer 60 0.181
106
ADL002 Adult Syndrome 70 0.180
107
INS024 Insulin-Like Growth Factor I 79 0.179
108
c SYS001 Systemic Lupus Erythematosus 86 0.178
109
TXC005 Toxic Shock Syndrome 62 0.178
110
HYP005 Hypokalemia 55 0.177
111
SKN019 Skin Melanoma 68 0.176
112
c LKM061 Leukemia, Acute Myeloid 84 0.175
113
END057 Endometrial Cancer 74 0.175
114
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.174
115
ANG054 Angina Pectoris 66 0.172
116
PRP027 Peripheral Vascular Disease 71 0.172
117
HLX001 Helix Syndrome 47 0.171
118
DFC004 Deficiency Anemia 70 0.170
119
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.170
120
P HYP086 Hypothyroidism 69 0.166
121
MCS002 Mucositis 56 0.166
122
P RCT021 Rectum Cancer 52 0.165
123
SRC014 Sarcoma 65 0.165
124
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.165
125
P ALP008 Alopecia 54 0.164
126
SPN035 Spindle Cell Sarcoma 53 0.164
127
ESP021 Esophageal Cancer 90 0.164
128
P ECL001 Eclampsia 50 0.163
129
c PRS136 Prostate Cancer, Hereditary, 6 33 0.162
130
c PRS130 Prostate Cancer, Hereditary, 8 32 0.162
131
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.162
132
P RSP003 Respiratory Failure 74 0.162
133
ATX019 Ataxia with Vitamin E Deficiency 42 0.162
134
URT010 Ureteral Obstruction 45 0.160
135
CHL014 Cholera 59 0.160
136
P PHC003 Pheochromocytoma 71 0.160
137
P FML187 Familial Hypertension 37 0.160
138
CRD132 Cardiac Conduction Defect 58 0.159
139
P GRF003 Graft-Versus-Host Disease 72 0.158
140
c MLG069 Malignant Hypertension 47 0.157
141
ADR040 Adrenal Gland Pheochromocytoma 46 0.157
142
PRT013 Portal Hypertension 59 0.157
143
MYL009 Myelodysplastic Syndrome 70 0.157
144
HMN044 Human Immunodeficiency Virus Type 1 71 0.156
145
c MCR129 Microvascular Complications of Diabetes 1 66 0.156
146
47X002 47,xyy 49 0.155
147
FCT007 Factor Vii Deficiency 67 0.154
148
SFT003 Soft Tissue Sarcoma 56 0.154
149
P HYP076 Hyperthyroidism 55 0.153
150
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.153
151
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.153
152
P ART021 Arteriosclerosis 54 0.152
153
P GLM040 Glioma Susceptibility 1 81 0.152
154
P MSC003 Muscular Atrophy 52 0.150
155
P PSR002 Psoriasis 62 0.149
156
P BPL003 Bipolar Disorder 56 0.148
157
P MYC008 Myocarditis 59 0.148
158
PST011 Pustulosis of Palm and Sole 52 0.148
159
c MJR024 Major Affective Disorder 9 41 0.148
160
c MJR022 Major Affective Disorder 8 38 0.148
161
DPR016 Depression 63 0.147
162
c MCR112 Microvascular Complications of Diabetes 2 41 0.147
163
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.147
164
RCK004 Rickets 68 0.146
165
c SCL052 Scleroderma, Familial Progressive 61 0.146
166
PLS009 Plasma Cell Neoplasm 51 0.146
167
OVR094 Ovarian Epithelial Cancer 38 0.146
168
IMP005 Impotence 52 0.145
169
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.145
170
AGN016 Aging 56 0.145
171
OST012 Osteoarthritis 78 0.145
172
P HYP061 Hypertrophic Cardiomyopathy 70 0.144
173
P LPS004 Lupus Erythematosus 61 0.144
174
THR024 Thrombosis 57 0.144
175
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.142
176
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.142
177
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.142
178
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.142
179
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.142
180
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.142
181
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.142
182
P LKM062 Leukemia, Acute Lymphoblastic 69 0.141
183
FTT001 Fatty Liver Disease 61 0.141
184
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.141
185
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.141
186
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.141
187
c ACT027 Acute Pancreatitis 60 0.141
188
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.141
189
P LKM071 Leukemia, Chronic Lymphocytic 79 0.141
190
P SLP006 Sleep Apnea 69 0.140
191
P PNM007 Pneumonia 68 0.139
192
STM007 Stomatitis 50 0.139
193
OST159 Osteogenic Sarcoma 66 0.138
194
c MGR028 Migraine with or Without Aura 1 67 0.138
195
PNC129 Pancreatic Adenocarcinoma 68 0.138
196
IMM167 Immune Deficiency Disease 78 0.137
197
PLM010 Pulmonary Edema 54 0.137
198
P RHM011 Rheumatoid Arthritis 80 0.137
199
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.137
200
ANX010 Anxiety 73 0.135
201
MNT002 Mental Depression 58 0.135
202
INT007 Intermediate Coronary Syndrome 55 0.134
203
c CHR064 Chronic Monocytic Leukemia 33 0.134
204
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.134
205
BNR002 Bone Resorption Disease 48 0.134
206
P AST007 Astrocytoma 51 0.133
207
c THR092 Thrombophilia Due to Thrombin Defect 73 0.133
208
SYS003 Systolic Heart Failure 49 0.133
209
P PLY014 Polycystic Kidney Disease 62 0.132
210
P DBT005 Diabetes Insipidus 55 0.132
211
GLC003 Glucose Intolerance 54 0.131
212
P HYP750 Hypertriglyceridemia, Familial 62 0.131
213
HRW001 Hair Whorl 36 0.131
214
ART074 Aortic Dissection 52 0.131
215
CNS004 Constipation 58 0.131
216
P MLG074 Malignant Mesenchymoma 40 0.130
217
P HPT021 Hepatitis 67 0.130
218
CRB004 Cerebral Artery Occlusion 45 0.129
219
P SYS005 Systemic Scleroderma 68 0.129
220
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.129
221
P OST002 Osteoporosis 74 0.129
222
P FCL005 Focal Segmental Glomerulosclerosis 57 0.128
223
c HPT001 Hepatitis C 62 0.128
224
P ART022 Arthritis 69 0.128
225
P UVT001 Uveitis 57 0.128
226
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.128
227
P PRD008 Periodontitis 64 0.127
228
NPH010 Nephrosclerosis 50 0.127
229
P INF038 Influenza 68 0.127
230
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.127
231
P HYP069 Hyperparathyroidism 63 0.127
232
BRN028 Brain Cancer 74 0.126
233
ACQ007 Acquired Immunodeficiency Syndrome 60 0.126
234
P MSC005 Muscular Dystrophy 66 0.126
235
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.125
236
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.124
237
c OVR114 Ovarian Cancer 1 38 0.124
238
TTN003 Tetanus 65 0.124
239
CRV035 Cervical Cancer 76 0.124
240
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.123
241
P ADL010 Adult Respiratory Distress Syndrome 65 0.123
242
HYP014 Hyperuricemia 52 0.122
243
ALC007 Alcohol Dependence 66 0.122
244
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.122
245
P CRD119 Cardiac Arrest 67 0.122
246
PNG002 Pain Agnosia 51 0.122
247
BRN071 Brain Injury 49 0.122
248
PRT058 Pure Autonomic Failure 59 0.122
249
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.120
250
PLM033 Pulmonary Embolism 59 0.120
251
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.120
252
P LNG064 Lung Cancer Susceptibility 3 78 0.120
253
SYN036 Syncope 45 0.119
254
c LKM063 Leukemia, Chronic Myeloid 72 0.119
255
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.119
256
c MTR002 Mitral Valve Insufficiency 48 0.119
257
ALD013 Aldosterone-Producing Adenoma 39 0.119
258
SCH014 Schistosomiasis 57 0.118
259
P NSP012 Nasopharyngeal Carcinoma 66 0.118
260
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.118
261
DYS073 Dysphagia 50 0.118
262
GRN017 Granulocytopenia 44 0.117
263
P ENC018 Encephalopathy 61 0.117
264
PRS045 Prostatic Hypertrophy 53 0.116
265
LYM027 Lymphopenia 58 0.116
266
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.116
267
P SZR006 Seizure Disorder 56 0.115
268
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.115
269
P INF032 Infertility 57 0.115
270
P FLL037 Follicular Lymphoma 67 0.115
271
P DMN002 Dementia 66 0.115
272
MRF001 Marfan Syndrome 77 0.115
273
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.115
275
P HDC001 Headache 57 0.115
276
DFF005 Diffuse Large B-Cell Lymphoma 55 0.114
277
ALL014 Allergic Encephalomyelitis 38 0.114
278
TRM010 Traumatic Brain Injury 51 0.113
279
P MJR001 Major Depressive Disorder 68 0.113
280
LYM040 Lymphoblastic Lymphoma 54 0.113
281
NNL006 Non-Alcoholic Steatohepatitis 54 0.113
282
c ACT073 Acute Leukemia 58 0.112
283
P PNC044 Pancreatitis 61 0.112
284
GLM044 Glomerular Disease 37 0.112
285
CRH001 Crohn's Disease 74 0.112
286
CRN030 Coronary Stenosis 50 0.112
287
CLT003 Colitis 62 0.111
288
P MYP004 Myopathy 70 0.111
289
P CNR004 Cone-Rod Dystrophy 2 73 0.111
290
CRD223 Cardiac Arrhythmia 60 0.110
291
HYP006 Hypertensive Heart Disease 49 0.110
292
P IGN003 Iga Nephropathy 1 49 0.110
293
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.110
294
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.109
295
PRS021 Prostatic Adenoma 51 0.109
296
PLM001 Pulmonary Tuberculosis 69 0.109
297
SVR004 Severe Combined Immunodeficiency 73 0.109
298
c ACT135 Acute Graft Versus Host Disease 52 0.108
299
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.108
300
HNS001 Hansen's Disease 34 0.108
301
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.108
302
P LPR021 Leprosy 3 69 0.108
303
HYD002 Hydronephrosis 60 0.108
304
P SKN015 Skin Carcinoma 66 0.108
305
SKN016 Skin Disease 63 0.108
306
PLM012 Pulmonary Sarcoidosis 53 0.108
307
PRS129 Prostatic Hyperplasia, Benign 49 0.107
308
HMT002 Hematologic Cancer 62 0.107
309
MDD011 Mood Disorder 62 0.107
310
c HRD002 Hereditary Angioedema 60 0.107
311
P MMB011 Membranous Nephropathy 50 0.107
312
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.107
313
MNT001 Mantle Cell Lymphoma 69 0.106
314
P ALC033 Alcohol Use Disorder 58 0.106
315
P URT039 Urticaria 58 0.106
316
P ESP024 Esophagitis 62 0.106
317
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.106
318
P PLY011 Polycystic Ovary Syndrome 56 0.106
319
DRM006 Dermatitis 61 0.105
320
CHL065 Cholangiocarcinoma 68 0.105
321
OLG003 Oligohydramnios 51 0.105
322
VSL002 Visual Epilepsy 59 0.105
323
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.104
324
THY029 Thyroid Carcinoma 59 0.104
325
INT079 Intrahepatic Cholangiocarcinoma 51 0.104
326
TRN018 Transitional Cell Carcinoma 56 0.103
327
SLC006 Silicosis 56 0.103
328
AST005 Asthma 76 0.103
329
PRT036 Peritonitis 64 0.103
330
PRP030 Purpura 54 0.103
331
HML018 Homologous Wasting Disease 22 0.103
332
BRN024 Bronchitis 68 0.103
333
P CRC039 Coarctation of Aorta 47 0.102
334
DPH001 Diphtheria 60 0.102
335
P GLY013 Glycogen Storage Disease 60 0.102
336
c HPT073 Hepatitis C Virus 72 0.102
337
PRP080 Peripheral Artery Disease 53 0.102
338
P VSC011 Vasculitis 62 0.101
339
DBT010 Diabetic Neuropathy 54 0.101
340
P INS002 in Situ Carcinoma 53 0.101
341
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.101
342
ANR004 Anuria 46 0.101
343
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.101
344
BRR014 Barrett Esophagus 65 0.101
345
P MLT020 Multiple Sclerosis 72 0.100
346
GST040 Gastric Adenocarcinoma 70 0.100
347
VSC002 Vascular Dementia 57 0.100
348
P SPP010 Suppressor of Tumorigenicity 3 51 0.100
349
MTB004 Metabolic Acidosis 50 0.100
350
URM002 Uremia 49 0.099
351
P CTR002 Cataract 60 0.099
352
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.099
353
ULC004 Ulcerative Colitis 73 0.099
354
c VRL010 Viral Hepatitis 52 0.098
355
TRN015 Transient Cerebral Ischemia 63 0.098
356
SPN186 Spinal Cord Injury 60 0.098
357
INT066 Interstitial Lung Disease 60 0.098
358
c FLL041 Follicular Lymphoma 1 49 0.098
359
P RTN024 Retinoblastoma 73 0.098
360
c FML008 Familial Retinoblastoma 53 0.098
361
c HPT016 Hepatitis B 59 0.098
362
P HRP006 Herpes Simplex 65 0.098
363
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.098
364
OCL069 Ocular Motor Apraxia 51 0.097
365
NTR005 Nutritional Deficiency Disease 62 0.097
366
c LKM005 Leukemia, T-Cell, Chronic 34 0.097
367
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.097
368
VCC001 Vaccinia 49 0.097
369
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.097
370
CHG001 Chagas Disease 66 0.097
371
HMR039 Hemorrhage, Intracerebral 57 0.097
372
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.096
373
ATS010 Autosomal Recessive Disease 48 0.096
374
SNS003 Sensory Peripheral Neuropathy 54 0.096
375
P PLY018 Polycythemia 56 0.096
376
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.095
377
P FBR017 Fibrosarcoma 56 0.095
378
P RHN004 Rhinitis 57 0.095
379
GLS001 Gliosarcoma 54 0.095
380
P PYL005 Pyelonephritis 56 0.094
381
SPL018 Splenomegaly 48 0.094
382
CNN005 Connective Tissue Disease 68 0.094
383
ATR057 Atrioventricular Block 55 0.093
384
P SYP003 Syphilis 58 0.093
385
P END044 Endometriosis 63 0.093
386
ADR016 Adrenal Cortical Carcinoma 48 0.093
387
P HYD006 Hydrocephalus 66 0.093
388
ANX004 Anoxia 40 0.093
389
P INF037 Inflammatory Bowel Disease 54 0.093
390
MSC157 Muscular Dystrophy, Duchenne Type 72 0.093
391
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.092
392
ATN005 Autonomic Dysfunction 46 0.092
393
ADR004 Adrenal Cortical Adenocarcinoma 39 0.092
394
P ART018 Aortic Valve Insufficiency 49 0.092
395
KPS004 Kaposi Sarcoma 75 0.092
396
P HYP120 Hypoaldosteronism 36 0.092
397
DST006 Diastolic Heart Failure 45 0.092
398
INT002 Intermittent Claudication 61 0.091
399
VRL011 Viral Infectious Disease 61 0.091
400
P LTR001 Lateral Sclerosis 54 0.091
401
IRN002 Iron Metabolism Disease 57 0.091
402
c ACT068 Acute Cystitis 63 0.091
403
LMB062 Limb Ischemia 55 0.091
404
P RHB003 Rhabdomyosarcoma 63 0.090
405
RTN020 Retinal Vascular Disease 46 0.090
406
CYS001 Cystic Fibrosis 81 0.090
407
P CHR345 Chronic Pain 44 0.090
408
CNN003 Conn's Syndrome 79 0.090
409
PPT005 Peptic Ulcer Disease 59 0.090
410
HYP114 Hypertensive Nephropathy 36 0.090
411
HRT012 Heart Valve Disease 53 0.090
412
P RTN018 Retinal Disease 53 0.090
414
P SCH015 Schizophrenia 74 0.090
415
P ENC004 Encephalitis 61 0.089
416
PST028 Post-Traumatic Stress Disorder 58 0.089
417
GT001 Gout 64 0.089
418
c WLM018 Wilms Tumor 5 61 0.089
419
NWB001 Newborn Respiratory Distress Syndrome 58 0.089
420
ACT084 Acute Stress Disorder 47 0.089
421
MSN001 Mesangial Proliferative Glomerulonephritis 45 0.088
422
c FML035 Familial Hyperlipidemia 55 0.088
423
P SML001 Small Cell Carcinoma 52 0.088
424
P GST044 Gastritis 56 0.088
425
c PNS012 Paine Syndrome 61 0.088
426
ACR007 Acromegaly 71 0.088
427
HRT011 Heart Septal Defect 50 0.088
428
CHL079 Children's Interstitial Lung Disease 26 0.087
429
P LMY004 Leiomyosarcoma 63 0.087
430
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.087
431
P AMY004 Amyloidosis 70 0.086
432
MLR004 Malaria 81 0.086
433
P SCK005 Sickle Cell Disease 50 0.086
434
CRD137 Cardiogenic Shock 47 0.086
435
c CHR417 Chronic Graft Versus Host Disease 57 0.086
436
MSL001 Measles 62 0.086
437
HDG004 Hodgkin's Granuloma 23 0.085
438
HDG006 Hodgkin's Paragranuloma 22 0.085
439
OVR029 Ovarian Hyperstimulation Syndrome 64 0.085
440
P HYP098 Hypereosinophilic Syndrome 67 0.085
441
EYD002 Eye Disease 58 0.085
442
GST023 Gastric Ulcer 53 0.085
443
OBS082 Obstructive Nephropathy 42 0.085
444
PPL052 Papillomatosis, Confluent and Reticulated 33 0.085
445
END040 Endogenous Depression 55 0.085
446
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.085
447
c VSC019 Vesicoureteral Reflux 1 57 0.084
448
c FML001 Familial Atrial Fibrillation 65 0.084
449
c HPT003 Hepatitis a 62 0.084
450
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.084
451
c BSL007 Basal Cell Carcinoma 68 0.084
452
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.083
453
c PRM005 Primary Hyperparathyroidism 58 0.083
454
BRK010 Burkitt Lymphoma 67 0.083
455
MCL006 Macular Retinal Edema 55 0.083
456
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.083
457
P MTR003 Mitral Valve Stenosis 50 0.083
458
BCT022 Bacterial Infectious Disease 56 0.083
459
CHL068 Cholestasis 61 0.083
460
c EXD008 Exudative Vitreoretinopathy 1 71 0.083
461
ART002 Arts Syndrome 64 0.083
462
MMB001 Membranoproliferative Glomerulonephritis 55 0.082
463
P PMP001 Pemphigus 54 0.082
464
CLN015 Colon Adenocarcinoma 65 0.081
465
c FNC043 Fanconi Anemia, Complementation Group E 62 0.081
466
P GCH001 Gaucher's Disease 63 0.081
467
c ART101 Aortic Valve Disease 2 65 0.081
468
RHM028 Rheumatic Heart Disease 53 0.081
469
ALL003 Allergic Rhinitis 67 0.081
470
P THY032 Thyroiditis 52 0.081
471
SCK003 Sickle Cell Anemia 74 0.081
472
IDP033 Idiopathic Edema 44 0.081
473
c SPN225 Spondyloarthropathy 1 73 0.081
474
c CHR682 Chronic Bilirubin Encephalopathy 39 0.080
475
c BRN108 Branchiootic Syndrome 1 62 0.080
476
c SCN007 Secondary Hyperparathyroidism 51 0.080
477
CLR109 Colorectal Adenocarcinoma 51 0.080
478
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.079
479
URN010 Urinary Tract Obstruction 55 0.079
480
P SBS003 Substance Abuse 55 0.079
481
HMC014 Homocysteinemia 53 0.079
482
ANR007 Anorexia Nervosa 63 0.079
483
CRT013 Carotid Stenosis 50 0.079
484
P SNS001 Sensorineural Hearing Loss 60 0.078
485
c FML021 Familial Hypercholesterolemia 66 0.078
486
P CHN012 Chondrosarcoma 56 0.078
487
SMN007 Seminoma 43 0.078
488
KHL003 Kohlschutter-Tonz Syndrome 65 0.078
489
P NRV007 Nervous System Disease 66 0.078
490
LSH001 Leishmaniasis 63 0.078
491
P KLZ004 Kala-Azar 1 41 0.078
492
P GRV001 Graves' Disease 55 0.077
493
c DRR009 Diarrhea 6 46 0.077
494
BRN004 Brain Edema 56 0.077
495
RTN017 Retinal Detachment 61 0.077
496
CRY004 Cryoglobulinemia 48 0.077
497
P DDN001 Duodenal Ulcer 52 0.077
498
THY030 Thyroid Gland Disease 52 0.077
499
P PNC025 Panic Disorder 53 0.077
500
P EPL164 Epilepsy 71 0.077
501
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.077
502
P PRK057 Parkinson Disease, Late-Onset 78 0.076
503
c NRF023 Neurofibromatosis, Type Ii 80 0.076
504
P THL005 Thalassemia 60 0.076
505
ATN004 Autonomic Neuropathy 45 0.076
506
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.076
507
P TRM003 Tremor 54 0.076
508
P OPT006 Optic Nerve Disease 60 0.076
509
BRN056 Bronchopulmonary Dysplasia 57 0.076
510
P PRL003 Proliferative Glomerulonephritis 44 0.075
511
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.075
512
BLR013 Biliary Tract Cancer 42 0.075
513
MRG003 Marginal Zone B-Cell Lymphoma 52 0.075
514
c GLY008 Glycogen Storage Disease Ii 70 0.075
515
GST045 Gastroenteritis 59 0.075
516
c SVR005 Severe Pre-Eclampsia 50 0.075
517
P MTR012 Mitral Valve Disease 58 0.075
518
P PSD003 Pseudohypoaldosteronism 44 0.075
519
49X006 49, Xxxxy Syndrome 41 0.075
520
GST033 Gestational Diabetes 61 0.075
521
P OPN001 Open-Angle Glaucoma 49 0.075
523
c PRD040 Periodontitis, Chronic 53 0.075
524
P OVR082 Overgrowth Syndrome 50 0.075
525
CRC021 Carcinosarcoma 62 0.074
526
P DRM053 Dermatitis, Atopic 66 0.074
527
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.074
528
MCP033 Mucopolysaccharidoses 38 0.074
529
P PRM006 Primary Biliary Cirrhosis 62 0.074
530
P HNT016 Huntington Disease 72 0.074
531
c PCH010 Pachyonychia Congenita 3 44 0.074
532
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.074
533
P CYS018 Cystitis 59 0.074
534
P SLP005 Sleep Disorder 59 0.074
535
HYP540 Hypertension, Diastolic 40 0.074
536
HMS001 Hemosiderosis 54 0.073
537
P PLY019 Polyneuropathy 56 0.073
538
P RNL028 Renal Tubular Dysgenesis 51 0.073
539
SXL003 Sexual Disorder 47 0.073
540
P ADL017 Adult T-Cell Leukemia 56 0.073
541
APN008 Apnea, Obstructive Sleep 64 0.073
542
P RRH023 Rare Hereditary Hemochromatosis 41 0.072
543
P CTN015 Cutaneous T Cell Lymphoma 49 0.072
544
END041 Endometrial Adenocarcinoma 63 0.072
545
P MLN007 Male Infertility 55 0.072
546
MNN042 Meningioma, Radiation-Induced 62 0.072
547
P VNT002 Ventricular Septal Defect 60 0.072
548
PTT037 Pituitary Tumors 44 0.072
549
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.072
550
c MNN043 Meningioma, Familial 74 0.071
551
INS001 Insulinoma 60 0.071
552
RDN001 Reading Disorder 40 0.071
553
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.071
554
MLG164 Malignant Epithelial Tumor of Ovary 26 0.071
555
IGR001 Ige Responsiveness, Atopic 59 0.071
556
MYL005 Myelofibrosis 70 0.071
557
MYC006 Mycosis Fungoides 66 0.071
558
DNT012 Dental Caries 53 0.071
559
SPN021 Spinal Meningioma 50 0.071
560
SCR001 Secretory Meningioma 41 0.071
561
DSS008 Disease of Mental Health 58 0.070
562
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.070
563
c WLM013 Wilms Tumor 1 65 0.070
564
c ATM022 Autoimmune Myocarditis 35 0.070
565
AMN003 Amnestic Disorder 54 0.070
566
P RNL007 Renal Tubular Acidosis 51 0.070
567
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.070
568
P ACT105 Acute Mountain Sickness 52 0.070
569
P ART005 Arteriovenous Malformation 65 0.070
570
TST014 Testicular Cancer 46 0.070
571
C1N001 C1 Inhibitor Deficiency 39 0.070
572
CYT008 Cytomegalovirus Infection 57 0.070
573
SPN051 Spondylitis 51 0.070
574
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.069
575
INF009 Inflammatory Spondylopathy 31 0.069
576
RYN005 Raynaud Phenomenon 47 0.069
577
ANG049 Angioedema Induced by Ace Inhibitors 40 0.069
578
CRV045 Cervical Intraepithelial Neoplasia 39 0.069
579
SBC016 Subacute Delirium 44 0.069
580
NRT001 Neurotic Disorder 53 0.069
581
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.069
582
P BND020 Bone Disease 59 0.069
583
P ORT004 Orthostatic Intolerance 62 0.069
584
DSS009 Disseminated Intravascular Coagulation 57 0.069
585
PLY150 Polykaryocytosis Inducer 31 0.069
586
P TTR001 Tetralogy of Fallot 70 0.069
587
VRC005 Varicose Veins 60 0.069
588
ARG004 Argyria 27 0.068
589
P HML001 Hemolytic-Uremic Syndrome 53 0.068
590
ERY051 Erythroleukemia, Familial 56 0.068
591
GTR002 Goiter 53 0.068
592
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.068
593
P MNN013 Meningitis 66 0.068
594
CLR030 Clear Cell Renal Cell Carcinoma 53 0.068
595
BRC012 Brucellosis 64 0.067
596
PLC008 Placenta Disease 50 0.067
597
P MJR007 Major Affective Disorder 1 43 0.067
598
P BRS044 Breast Adenocarcinoma 59 0.067
599
PLY001 Polycythemia Vera 69 0.067
600
P MLT074 Multiple Endocrine Neoplasia 56 0.067
601
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.067
602
CNT047 Contact Dermatitis 58 0.066
603
P EHL001 Ehlers-Danlos Syndrome 58 0.066
604
P CHL066 Cholangitis 51 0.066
605
LYS002 Lysosomal Storage Disease 52 0.066
606
CHR074 Choriocarcinoma 47 0.066
607
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.066
608
P PLM034 Pulmonary Emphysema 55 0.066
609
NPH009 Nephrolithiasis 55 0.066
610
P LYM033 Lymphoproliferative Syndrome 59 0.066
611
P CRY007 Cryoglobulinemia, Familial Mixed 50 0.066
612
c GLC092 Glaucoma, Primary Open Angle 62 0.066
613
FNG017 Fungal Infectious Disease 53 0.065
614
PLS025 Plasmablastic Lymphoma 47 0.065
615
PSY004 Psychotic Disorder 67 0.065
616
c GRV008 Graves Disease 1 56 0.065
617
THY122 Thyroid Gland Cancer 57 0.065
618
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.065
619
CRN322 Coronavirus Infectious Disease 40 0.065
620
P GLL018 Gallbladder Cancer 57 0.065
621
PSR001 Psoriatic Arthritis 61 0.064
622
P THR015 Thrombophilia 51 0.064
623
BCK006 Back Pain 42 0.064
624
DBT006 Diabetic Macular Edema 48 0.064
625
OCL006 Ocular Hypertension 53 0.064
626
SKN013 Skin Benign Neoplasm 51 0.064
627
PLC002 Plica Syndrome 36 0.064
628
GLS018 Glass Syndrome 57 0.064
629
P END033 Endocarditis 57 0.064
630
SYN007 Synovitis 54 0.064
631
GST071 Gastrointestinal Carcinoma 47 0.064
632
SNG003 Single Ventricular Heart 30 0.063
633
c MJR003 Major Affective Disorder 6 33 0.063
634
c MJR006 Major Affective Disorder 5 33 0.063
635
KLD004 Keloid Disorder 40 0.063
636
P CLC063 Celiac Disease 1 66 0.063
637
P MNC007 Monocytic Leukemia 53 0.063
638
ADR005 Adrenal Carcinoma 58 0.063
639
SPR126 Superior Semicircular Canal Dehiscence 40 0.063
640
c HMG029 Hemoglobin Se Disease 39 0.063
641
PNC001 Pancytopenia 54 0.062
642
P ALP009 Alopecia Areata 60 0.062
643
HYP081 Hypolipoproteinemia 51 0.062
644
ANT018 Anthracosis 48 0.062
645
HDN002 Head Injury 46 0.062
646
TRP009 Triple X Syndrome 42 0.062
647
HLC007 Helicobacter Pylori Infection 59 0.062
648
MDD018 Middle East Respiratory Syndrome 43 0.062
649
KWS002 Kawasaki Disease 65 0.062
650
PRC013 Pericarditis 54 0.062
651
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.062
652
ART017 Aortic Disease 49 0.062
653
P ART023 Arthropathy 62 0.062
654
c INF071 Inflammatory Bowel Disease 1 67 0.062
655
PST092 Posttransplant Acute Limbic Encephalitis 29 0.062
656
CHC001 Chickenpox 60 0.061
657
GRM010 Germ Cells Tumors 34 0.061
658
GST092 Gastroesophageal Reflux 67 0.061
659
P APL001 Aplastic Anemia 74 0.061
660
P ALP004 Alport Syndrome 68 0.061
661
IDP091 Idiopathic Nephrotic Syndrome 42 0.061
662
ATM052 Autoimmune Disease 1 37 0.061
663
P HML002 Hemolytic Anemia 63 0.061
664
P TRT010 Teratoma 52 0.061
665
P PNM006 Pneumoconiosis 56 0.061
666
ORL015 Oral Squamous Cell Carcinoma 43 0.061
667
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.061
668
OST003 Osteonecrosis 61 0.061
669
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.061
670
P MGR001 Migraine Without Aura 49 0.061
671
RSP007 Respiratory Distress Syndrome, Infant 30 0.061
672
IDP011 Idiopathic Interstitial Pneumonia 59 0.061
673
P TRC086 Trichohepatoenteric Syndrome 1 62 0.060
674
RHM001 Rheumatic Fever 60 0.060
675
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.060
676
BRS099 Breast Ductal Carcinoma 62 0.060
677
HYP017 Hypophosphatemia 50 0.060
678
EXT034 Extrinsic Allergic Alveolitis 58 0.060
679
CRT017 Cartilage Disease 54 0.060
680
CRH005 Crohn's Colitis 53 0.060
681
PPL001 Papillary Adenoma 44 0.060
682
P BNC003 Bone Cancer 58 0.060
683
P PTN014 Patent Ductus Arteriosus 1 60 0.060
684
PLY100 Polyploidy 40 0.060
685
HST010 Histiocytosis 48 0.059
686
c MJR008 Major Affective Disorder 2 35 0.059
687
CRN020 Coronary Restenosis 39 0.059
688
LMY002 Leiomyoma 52 0.059
689
CRN017 Coronary Thrombosis 47 0.059
690
CRV038 Cervical Squamous Cell Carcinoma 58 0.059
691
c MJR023 Major Affective Disorder 7 33 0.059
692
c MJR004 Major Affective Disorder 4 28 0.059
693
HYP025 Hyperphosphatemia 48 0.059
694
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.059
695
HRY003 Hairy Cell Leukemia 55 0.059
696
ACT003 Acute Kidney Tubular Necrosis 45 0.059
697
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 68 0.059
698
P MGR003 Migraine with Aura 52 0.059
699
c ART115 Aortic Valve Disease 1 75 0.059
700
P OBS001 Obstructive Jaundice 50 0.058
701
ETN001 Eating Disorder 60 0.058
702
PRP016 Paraplegia 52 0.058
703
HYP781 Hypoascorbemia 51 0.058
704
LPT014 Leptin Deficiency or Dysfunction 74 0.058
705
SPN209 Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations 66 0.058
706
INT067 Interstitial Nephritis 48 0.058
707
SPP011 Suppression of Tumorigenicity 12 59 0.058
708
PNM008 Pneumothorax 56 0.058
709
ALL006 Allergic Asthma 56 0.058
710
P ATS364 Autism 70 0.058
711
HYP457 Hypertrophic Scars 42 0.058
712
HPT004 Hepatic Coma 45 0.058
713
DCT002 Ductal Carcinoma in Situ 59 0.057
714
ACT119 Acute Promyelocytic Leukemia 63 0.057
715
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.057
716
P HYP265 Hypotonia 43 0.057
717
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.057
718
HRP004 Herpes Zoster 60 0.057
719
STT001 Status Epilepticus 60 0.057
720
P LRY044 Larynx Cancer 55 0.056
721
AZS001 Azoospermia 50 0.056
722
CKT002 Cakut 48 0.056
723
AMN001 Amenorrhea 54 0.056
724
CRT015 Carotid Artery Occlusion 45 0.056
725
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.056
726
P TMP001 Temporal Lobe Epilepsy 50 0.056
727
EMB004 Embryonal Carcinoma 56 0.056
728
TBC004 Tobacco Addiction 64 0.056
729
CRT016 Carotid Artery Disease 52 0.056
730
MLT157 Multiple System Atrophy 1 70 0.056
731
CRB086 Cerebral Aneurysms 40 0.056
732
INF034 Infective Endocarditis 53 0.056
733
IRR002 Irritable Bowel Syndrome 65 0.055
734
SZR001 Sezary's Disease 60 0.055
735
SPS057 Spasticity 45 0.055
736
c HNT011 Huntington Disease-Like 3 38 0.055
737
ART004 Aortic Atherosclerosis 47 0.055
738
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.055
739
GNG013 Gingivitis 59 0.055
740
ORL011 Oral Cancer 60 0.055
741
ADR041 Adrenal Cortical Adenoma 43 0.055
742
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.055
743
BRN002 Bronchiolitis 59 0.055
744
P OTS001 Otosclerosis 49 0.055
745
AVN001 Avian Influenza 59 0.055
746
HPT019 Hepatic Encephalopathy 60 0.054
747
PMP006 Pemphigus Vulgaris, Familial 57 0.054
748
NRT004 Neuritis 52 0.054
749
KRT019 Keratitis, Hereditary 65 0.054
750
ILS001 Ileus 51 0.054
751
ASP007 Aspiration Pneumonia 48 0.054
752
PLR008 Pleurisy 50 0.054
753
P HMN010 Hemangioma 61 0.054
754
c HYP272 Hypercholesterolemia, Familial, 3 44 0.054
755
OST017 Osteomyelitis 64 0.054
756
HMP001 Hemopericardium 48 0.054
757
SKL017 Skeletal Dysplasias 40 0.054
758
THR123 Thrombotic Microangiopathy 36 0.054
759
ALL010 Allergic Contact Dermatitis 56 0.053
760
P ESS003 Essential Thrombocythemia 68 0.053
761
c ATM011 Autoimmune Hepatitis 63 0.053
762
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.053
763
ENT011 Enterocolitis 51 0.053
764
HYP080 Hypogonadism 50 0.053
765
FBR012 Fabry Disease 72 0.053
766
ADR008 Adrenal Adenoma 55 0.053
767
KDN013 Kidney Hypertrophy 32 0.053
768
c ALP101 Alpha-Thalassemia 62 0.053
769
P PRC012 Pericardial Effusion 51 0.053
770
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.053
771
P MCR010 Microcephaly 59 0.053
772
SPL004 Splenic Marginal Zone Lymphoma 51 0.053
773
PNC034 Pancreas Disease 48 0.053
774
P RTN016 Retinal Degeneration 53 0.053
775
c DPH024 Diaphragmatic Hernia, Congenital 63 0.053
776
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.053
777
MTH009 Mouth Disease 56 0.052
778
CYN002 Cyanosis, Transient Neonatal 45 0.052
779
P ATR010 Atrial Heart Septal Defect 60 0.052
780
c TRC022 Tricuspid Valve Insufficiency 45 0.052
781
RST023 Resting Heart Rate, Variation in 41 0.052
782
THY111 Thyroid Carcinoma, Familial Medullary 67 0.052
783
CLF027 Cleft Palate, Isolated 64 0.052
784
GST020 Gastric Antral Vascular Ectasia 41 0.052
785
c PNC106 Pancreatic Agenesis 1 51 0.052
786
P INT070 Intestinal Obstruction 58 0.052
787
c PST041 Posterior Urethral Valves 41 0.052
788
NRS005 Neurosarcoidosis 36 0.052
789
LKS001 Leukostasis 46 0.051
790
PRD004 Prediabetes Syndrome 47 0.051
791
PRM329 Premature Aging 35 0.051
792
c LKM070 Leukemia, Acute Monocytic 57 0.051
793
P DRM010 Dermatomyositis 61 0.051
794
HPT022 Hepatoblastoma 56 0.051
795
INT030 Intracranial Aneurysm 56 0.051
796
P SJG008 Sjogren Syndrome 61 0.051
797
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.051
798
ASB001 Asbestosis 47 0.051
799
ASB003 Asbestos Intoxication 26 0.051
800
P TBR001 Tuberous Sclerosis 70 0.051
801
P LCH002 Lichen Planus 53 0.051
802
c JVN010 Juvenile Rheumatoid Arthritis 64 0.051
803
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.051
804
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.051
805
P AVS003 Avascular Necrosis 42 0.051
806
ALC010 Alcoholic Cardiomyopathy 42 0.051
807
HPT014 Hepatorenal Syndrome 50 0.050
808
VRC001 Varicocele 49 0.050
809
ALB002 Albinism 46 0.050
810
P MYS005 Myositis 56 0.050
811
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.050
812
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.050
813
QDR001 Quadriplegia 48 0.050
814
TST043 Testicular Seminoma 35 0.050
815
CYT018 Cytochrome P450 2d6 Variant 27 0.050
816
P CLS010 Cluster Headache 42 0.050
817
DBT002 Diabetic Autonomic Neuropathy 41 0.050
818
GST050 Gastrointestinal System Disease 56 0.050
819
ECT026 Ectopic Pregnancy 50 0.050
820
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.050
821
P PRC031 Preeclampsia/eclampsia 1 38 0.050
822
P BRT004 Bartter Disease 52 0.049
823
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.049
824
FBR047 Fibromyalgia 58 0.049
825
c ACT076 Acute Myocarditis 46 0.049
826
DMY004 Demyelinating Disease 52 0.049
827
CMP040 Complement Component 4, Partial Deficiency of 33 0.049
828
CHR066 Chronic Fatigue Syndrome 61 0.049
829
LNG108 Langerhans Cell Histiocytosis 58 0.049
830
HYP043 Hyperandrogenism 48 0.049
831
P VNW001 Von Willebrand's Disease 65 0.049
832
VSC003 Visceral Leishmaniasis 55 0.049
833
DBT008 Diabetic Angiopathy 44 0.048
834
IMM001 Immune-Complex Glomerulonephritis 40 0.048
835
P END084 Endocrine System Disease 45 0.048
836
HYP264 Hypertonia 38 0.048
837
c CHR098 Chronic Pyelonephritis 38 0.048
838
THY125 Thyroid Gland Medullary Carcinoma 50 0.048
839
P HYP055 Hypoplastic Left Heart Syndrome 63 0.048
840
P OCL013 Oculodentodigital Dysplasia 69 0.048
841
P SCK002 Sick Sinus Syndrome 55 0.048
842
HSH003 Hashimoto Thyroiditis 62 0.048
843
YLL002 Yellow Fever 61 0.048
844
CMP010 Complex Regional Pain Syndrome 58 0.048
845
PRC003 Proctitis 47 0.048
846
c MCR256 Microphthalmia, Syndromic 9 56 0.048
847
P SCL009 Sclerosing Cholangitis 48 0.048
848
P TST021 Testicular Germ Cell Tumor 60 0.047
849
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.047
850
PRS063 Paresthesia 41 0.047
851
HMT008 Hematuria, Benign Familial 56 0.047
852
SCH012 Schizoaffective Disorder 50 0.047
853
CCN001 Cocaine Dependence 48 0.047
854
MYC005 Myocardial Stunning 46 0.047
855
RSP006 Respiratory System Disease 50 0.047
856
BRN012 Bronchiolitis Obliterans 55 0.047
857
c INF145 Infantile Liver Failure Syndrome 1 50 0.047
858
c BSL024 Basal Cell Carcinoma 1 56 0.047
859
URT049 Urate Oxidase, Pseudogene 25 0.047
860
LCH001 Leech Infestation 35 0.047
861
MST020 Mast Cell Activation Syndrome 26 0.047
862
P ANT006 Antiphospholipid Syndrome 55 0.047
863
c ALM001 Al Amyloidosis 50 0.047
864
P ATR005 Atrophic Gastritis 50 0.047
865
P OCL002 Oculocutaneous Albinism 60 0.047
866
P MYC033 Myoclonus 46 0.047
867
ANV001 Anovulation 47 0.047
868
GNG012 Gingival Overgrowth 51 0.047
869
P MTR014 Motor Neuron Disease 65 0.046
870
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.046
871
IMM136 Immune System Disease 45 0.046
872
RNL078 Renal Dysplasia 50 0.046
873
FBR032 Fibromuscular Dysplasia 48 0.046
874
c CNT015 Central Sleep Apnea 45 0.046
875
PLC005 Placental Insufficiency 57 0.046
876
ACR041 Acromelic Frontonasal Dysostosis 52 0.046
877
P PLY041 Polymyositis 57 0.046
878
c ACT134 Acute Liver Failure 56 0.046
879
P CLL015 Collagen Disease 47 0.046
880
MCR011 Microinvasive Gastric Cancer 43 0.046
881
c HRD202 Hereditary Lymphedema I 50 0.046
882
CHL149 Childhood Acute Myeloid Leukemia 44 0.046
883
c CHL119 Cholangitis, Primary Sclerosing 57 0.046
884
HST011 Histoplasmosis 55 0.046
885
CCN002 Cocaine Abuse 49 0.046
886
c CLR017 Clear Cell Sarcoma 45 0.046
887
ACT200 Acute Monoblastic Leukemia 52 0.045
888
FDL002 Food Allergy 51 0.045
889
ACT029 Acute Interstitial Pneumonia 49 0.045
890
PST053 Postherpetic Neuralgia 40 0.045
891
MCL003 Macular Holes 40 0.045
892
c PRG020 Paragangliomas 3 39 0.045
893
HMG002 Hemoglobinuria 50 0.045
894
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.045
895
P OPT009 Optic Neuritis 57 0.045
896
STT041 Stuttering 52 0.045
897
GLC008 Glucose Metabolism Disease 40 0.045
898
HNC001 Henoch-Schoenlein Purpura 55 0.045
899
DXR001 Doxorubicin Induced Cardiomyopathy 33 0.045
900
APP008 Appendicitis 61 0.045
901
P PTT006 Pituitary Adenoma 55 0.045
902
MXD005 Mixed Connective Tissue Disease 58 0.045
903
P CYS039 Cystic Kidney Disease 54 0.045
904
GTL001 Gitelman Syndrome 65 0.045
905
HMP005 Hemiplegia 55 0.044
906
P SLM003 Salmonellosis 55 0.044
907
SCH003 Schizophreniform Disorder 56 0.044
908
P HYP838 Hyperlipidemia, Familial Combined, 3 56 0.044
909
P HYP083 Hypopituitarism 53 0.044
910
PRS047 Prostatitis 56 0.044
911
HYP034 Hypertensive Encephalopathy 46 0.044
912
APH002 Aphasia 57 0.044
913
CRS001 Crescentic Glomerulonephritis 43 0.044
914
GST037 Gastroparesis 54 0.044
915
ADR007 Adrenoleukodystrophy 75 0.044
916
c DWL002 Dowling-Degos Disease 1 58 0.044
917
URL001 Urolithiasis 45 0.044
918
c SYS043 Systemic Lupus Erythematosus 1 38 0.044
919
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.043
920
P CRN037 Craniosynostosis 68 0.043
921
P BRN022 Bronchiectasis 59 0.043
922
c ANG068 Angioedema, Hereditary, Type I 57 0.043
923
INT075 Intracranial Hypertension 53 0.043
924
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.043
925
P MLT007 Multiple Epiphyseal Dysplasia 58 0.043
926
LMY014 Leiomyoma, Uterine 56 0.043
927
ART010 Arteriolosclerosis 37 0.043
928
P PRP029 Porphyria 62 0.043
929
P HMN036 Hemangiopericytoma, Malignant 59 0.043
930
c TBR025 Tuberous Sclerosis 1 77 0.043
931
KHN001 Kuhnt-Junius Degeneration 47 0.043
932
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 0.043
933
c VRL005 Viral Pneumonia 52 0.043
934
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 0.043
935
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.043
936
PRS042 Prostate Disease 43 0.043
937
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.043
938
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.043
939
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.043
940
c MCL013 Mucolipidosis Iv 66 0.043
941
NRM001 Neuromyelitis Optica 61 0.043
942
TNS005 Tonsillitis 57 0.043
943
P OVR049 Ovarian Disease 52 0.043
944
RNL097 Renal Artery Disease 42 0.043
945
FCL012 Facial Paralysis 46 0.043
946
c BTT014 Beta-Thalassemia 74 0.042
947
BRS051 Breast Disease 58 0.042
948
MRD002 Marden-Walker Syndrome 56 0.042
949
c FCL025 Focal Segmental Glomerulosclerosis 1 46 0.042
950
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 0.042
951
c ACQ012 Acquired Angioedema 38 0.042
952
WLF001 Wolff-Parkinson-White Syndrome 66 0.042
953
HYP020 Hyperprolactinemia 64 0.042
954
P ACT010 Acth-Secreting Pituitary Adenoma 55 0.042
955
ESP002 Esophageal Varix 51 0.042
956
SNT005 Sinoatrial Node Disease 49 0.042
957
AGR002 Agoraphobia 45 0.042
958
PLY012 Polyhydramnios 46 0.042
959
c HYP768 Hyperlipoproteinemia, Type I 67 0.042
960
P GLL022 Guillain-Barre Syndrome 59 0.042
961
PPT001 Peptic Esophagitis 52 0.042
962
P LCT001 Lactic Acidosis 51 0.042
963
GYN001 Gynecomastia 49 0.042
964
MNN020 Meningococcal Infection 46 0.042
965
PMP004 Pemphigus Foliaceus 43 0.042
966
INF021 Infant Gynecomastia 31 0.042
967
P ANT001 Anterolateral Myocardial Infarction 34 0.042
968
ALC009 Alcoholic Liver Cirrhosis 53 0.041
969
NTR046 Neutrophil Migration 50 0.041
970
EBL001 Ebola Hemorrhagic Fever 49 0.041
971
ADR048 Adrenal Hyperplasia, Congenital, Due to 3-Beta-Hydroxysteroid Dehydrogenase 2 Deficiency 37 0.041
973
HYP008 Hypertensive Retinopathy 39 0.041
974
c RNL113 Renal Failure, Progressive, with Hypertension 34 0.041
975
ING001 Inguinal Hernia 60 0.041
976
CHL004 Cholelithiasis 49 0.041
977
LYM051 Lymphomatoid Granulomatosis 45 0.041
978
P CHR012 Chronic Granulomatous Disease 67 0.041
979
CHR100 Chronic Ulcer of Skin 55 0.041
980
LPR001 Lepromatous Leprosy 50 0.041
981
LFT001 Left Bundle Branch Hemiblock 49 0.041
982
WST005 West Nile Virus 54 0.041
983
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.041
984
LPT006 Leptin Receptor Deficiency 48 0.041
985
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.041
986
c MCP052 Mucopolysaccharidosis, Type Vi 67 0.041
987
ALK024 Alkuraya-Kucinskas Syndrome 51 0.041
988
c ACT042 Acute Pyelonephritis 46 0.041
989
CNG506 Congenital Amyoplasia 27 0.041
990
OVR063 Overnutrition 44 0.041
991
CRD016 Cardiac Rupture 37 0.041
992
HPT046 Hepatic Veno-Occlusive Disease 56 0.040
993
SLP001 Sleeping Sickness 54 0.040
994
CHR176 Chromophil Renal Cell Carcinoma 23 0.040
995
IRD001 Iridocyclitis 53 0.040
996
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.040
997
PGM001 Pigmented Villonodular Synovitis 56 0.040
998
LST001 Listeriosis 56 0.040
999
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.040
1000
P NRC002 Narcolepsy 52 0.040
1001
NSS002 Neisseria Meningitidis Infection 47 0.040
1002
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.040
1003
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 46 0.040
1004
THR099 Third-Degree Atrioventricular Block 45 0.040
1005
c PLM022 Pulmonary Valve Insufficiency 39 0.040
1006
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.040
1007
P PLY017 Polyarteritis Nodosa 58 0.040
1008
P PRM002 Primary Hyperoxaluria 62 0.040
1009
NRG002 Neurogenic Bladder 55 0.040
1010
P RTN022 Retinal Vein Occlusion 53 0.040
1011
PLR007 Pleural Empyema 50 0.040
1012
END062 Endometrial Hyperplasia 48 0.040
1013
TNG009 Tongue Squamous Cell Carcinoma 44 0.040
1014
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.040
1015
MGL001 Megaloblastic Anemia 51 0.040
1016
KRT002 Keratomalacia 47 0.040
1017
PST048 Postural Orthostatic Tachycardia Syndrome 45 0.040
1018
P FML018 Familial Mediterranean Fever 73 0.039
1019
HYD038 Hydrops Fetalis, Nonimmune 62 0.039
1020
MYP159 Myopathy, Proximal, with Ophthalmoplegia 55 0.039
1021
SCH036 Scheie Syndrome 72 0.039
1022
P MTR004 Maturity-Onset Diabetes of the Young 65 0.039
1023
c BCT007 Bacterial Meningitis 55 0.039
1024
P MTH007 Methemoglobinemia 46 0.039
1025
P TST026 Testicular Germ Cell Cancer 43 0.039
1026
DFF003 Diffuse Scleroderma 41 0.039
1027
DNS007 Dense Deposit Disease 37 0.039
1028
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 53 0.039
1029
P TMP003 Temporal Arteritis 68 0.039
1030
VTM027 Vitamin D-Dependent Rickets, Type 2a 56 0.039
1031
P VNS003 Venous Insufficiency 55 0.039
1032
CHR073 Choreatic Disease 52 0.039
1033
c BCT013 Bacterial Pneumonia 48 0.039
1034
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.039
1035
KWS001 Kwashiorkor 44 0.039
1036
P FML011 Familial Adenomatous Polyposis 72 0.039
1037
P MVM001 Movement Disease 63 0.039
1038
OVR112 Ovarian Germ Cell Cancer 45 0.039
1039
P HRM001 Hermansky-Pudlak Syndrome 64 0.039
1040
P ESP035 Esophagitis, Eosinophilic, 1 57 0.039
1041
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.039
1042
GSG001 Gas Gangrene 53 0.039
1043
FML037 Female Breast Cancer 52 0.039
1044
c BNG021 Benign Essential Hypertension 26 0.039
1045
END021 Endomyocardial Fibrosis 49 0.038
1046
c NPH049 Nephrotic Syndrome, Type 2 48 0.038
1047
CRN019 Coronary Artery Vasospasm 46 0.038
1048
c FML015 Familial Nephrotic Syndrome 41 0.038
1049
TLM001 Telomere Length, Mean Leukocyte 19 0.038
1050
ONC002 Onchocerciasis 52 0.038
1051
HRP008 Herpes Simiae 25 0.038
1052
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 0.038
1053
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.038
1054
P VTR007 Vitreoretinopathy 46 0.038
1055
P INT143 Interstitial Cystitis 61 0.038
1056
CHK001 Chikungunya 57 0.038
1057
CLS052 Classic Hairy Cell Leukemia 27 0.038
1058
P HML033 Hemolytic Uremic Syndrome, Atypical 1 68 0.038
1059
P LMB006 Limb-Girdle Muscular Dystrophy 53 0.038
1060
P PRD021 Periodic Paralysis 45 0.038
1061
HYP344 Hyperthyroidism, Familial Gestational 39 0.038
1062
FBR019 Fibromatosis 41 0.038
1063
P TRC031 Trichorhinophalangeal Syndrome 40 0.038
1064
TRD006 Tardive Dyskinesia 54 0.038
1065
GRM004 Germinoma 40 0.038
1066
FNT004 Fainting 30 0.037
1067
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 0.037
1068
c PRM196 Premature Ovarian Failure 1 67 0.037
1069
P DST002 Distal Arthrogryposis 63 0.037
1070
CRN027