Search results for angiotensin I

1489 hits were found for angiotensin I

# Family MCID Name MIFTS Score
1
c HYP595 Hypertension, Essential 84 0.588
2
CNG034 Congestive Heart Failure 69 0.518
3
P KDN018 Kidney Disease 72 0.506
4
c MCR113 Microvascular Complications of Diabetes 3 52 0.505
5
c MCR120 Microvascular Complications of Diabetes 7 47 0.497
6
c MCR130 Microvascular Complications of Diabetes 6 41 0.497
7
c MCR133 Microvascular Complications of Diabetes 4 41 0.497
8
INS024 Insulin-Like Growth Factor I 79 0.487
9
c CHR684 Chronic Kidney Disease 70 0.404
10
P HRT032 Heart Disease 75 0.398
11
END086 End Stage Renal Disease 51 0.351
12
P MYC007 Myocardial Infarction 70 0.332
13
P SRC025 Sarcoidosis 1 70 0.331
14
P VSC007 Vascular Disease 63 0.328
15
P ANG015 Angioedema 57 0.316
16
LPP008 Lipoprotein Quantitative Trait Locus 62 0.311
17
P CRN300 Coronary Heart Disease 1 63 0.305
18
ATH013 Atherosclerosis Susceptibility 65 0.302
19
PRT037 Pertussis 65 0.296
20
c PRC016 Pre-Eclampsia 63 0.291
21
P DBT009 Diabetes Mellitus 64 0.283
22
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.280
23
P RNV001 Renovascular Hypertension 48 0.280
24
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.278
25
P LNG032 Lung Cancer 98 0.270
26
c ACT075 Acute Myocardial Infarction 57 0.268
27
P NTR004 Neutropenia 63 0.266
28
P GLM007 Glomerulonephritis 57 0.263
29
ISC004 Ischemia 58 0.256
30
ART140 Arteries, Anomalies of 52 0.256
31
CVD001 Covid-19 44 0.254
32
P MCR115 Microvascular Complications of Diabetes 5 66 0.250
33
ART016 Aortic Aneurysm 69 0.248
34
P CRD246 Cardiovascular System Disease 57 0.247
35
c SVR001 Severe Acute Respiratory Syndrome 62 0.245
36
ANR040 Aneurysm 59 0.235
37
HYP066 Hyperglycemia 61 0.233
38
LVR012 Liver Cirrhosis 62 0.233
39
c DBT099 Diabetes Mellitus, Type I 65 0.229
40
P BRS047 Breast Cancer 97 0.228
41
P ATR011 Atrial Fibrillation 66 0.224
42
c SML038 Small Cell Cancer of the Lung 65 0.222
43
c ACT071 Acute Kidney Failure 60 0.221
44
RNL077 Renal Fibrosis 47 0.221
45
c ATR087 Atrial Standstill 1 75 0.219
46
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.218
47
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.218
48
P LYM118 Lymphoma 68 0.217
49
STR067 Stroke, Ischemic 81 0.217
50
P LVR013 Liver Disease 68 0.215
51
P RNL015 Renal Hypertension 47 0.214
52
P NRB001 Neuroblastoma 72 0.214
53
MSC007 Muscle Hypertrophy 64 0.213
54
ATM095 Autoimmune Disease 62 0.211
55
48X005 48,xyyy 39 0.210
56
c HYP836 Hypercholesterolemia, Familial, 1 73 0.208
57
P PLM037 Pulmonary Hypertension 67 0.207
58
HYP056 Hypoglycemia 66 0.206
59
P ADN016 Adenocarcinoma 64 0.204
60
P PNC035 Pancreatic Cancer 84 0.203
61
P LKM002 Leukemia 68 0.202
62
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.201
63
c LKM005 Leukemia, T-Cell, Chronic 34 0.200
64
HYP266 Hypoxia 57 0.199
65
LPD008 Lipid Metabolism Disorder 62 0.198
66
c DLT002 Dilated Cardiomyopathy 79 0.196
67
DWN001 Down Syndrome 70 0.195
68
P PRS040 Prostate Cancer 97 0.194
69
P EXN002 Exanthem 57 0.194
70
P CLR023 Colorectal Cancer 99 0.193
71
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.193
72
c SYS001 Systemic Lupus Erythematosus 86 0.193
73
ALL026 Allergic Hypersensitivity Disease 62 0.192
74
P NRP001 Neuropathy 56 0.191
75
P ALZ034 Alzheimer Disease 88 0.190
76
P OVR042 Ovarian Cancer 88 0.190
77
P NPH012 Nephrotic Syndrome 60 0.189
78
LNG099 Lung Disease 60 0.189
79
IGG001 Iga Glomerulonephritis 48 0.187
80
c PRM038 Primary Agammaglobulinemia 44 0.186
81
CRB039 Cerebrovascular Disease 67 0.186
82
LYM019 Lymphosarcoma 46 0.185
83
P BPL003 Bipolar Disorder 56 0.183
84
HYP060 Hyperinsulinism 54 0.183
85
P PLM036 Pulmonary Fibrosis 65 0.183
86
c MJR024 Major Affective Disorder 9 41 0.182
87
c MJR022 Major Affective Disorder 8 38 0.182
88
CYT002 Cytokine Deficiency 42 0.182
89
ADN018 Adenoma 59 0.176
90
P GLM045 Glioma 63 0.175
91
GLL048 Glial Tumor 45 0.175
92
ADL002 Adult Syndrome 70 0.175
93
P DRR001 Diarrhea 55 0.174
94
HLX001 Helix Syndrome 47 0.173
95
END057 Endometrial Cancer 74 0.172
96
HMN044 Human Immunodeficiency Virus Type 1 71 0.170
97
HYP005 Hypokalemia 55 0.170
98
GLB015 Glioblastoma Multiforme 75 0.169
99
P MYL006 Myeloid Leukemia 60 0.166
100
c SCL052 Scleroderma, Familial Progressive 61 0.166
101
P MLN008 Melanoma 69 0.166
102
ANG054 Angina Pectoris 66 0.165
103
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.165
104
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.164
105
P HYP086 Hypothyroidism 69 0.164
106
P HYP061 Hypertrophic Cardiomyopathy 70 0.163
107
P HYP076 Hyperthyroidism 55 0.163
108
P TRN020 Turner Syndrome 67 0.162
109
MYL069 Myeloma, Multiple 85 0.161
110
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.161
111
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.160
112
P ECL001 Eclampsia 50 0.158
113
CHL014 Cholera 59 0.157
114
P THR014 Thrombocytopenia 67 0.156
115
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.155
116
c LKM061 Leukemia, Acute Myeloid 84 0.155
117
P HPT023 Hepatocellular Carcinoma 100 0.155
118
BNR002 Bone Resorption Disease 48 0.154
119
PRP027 Peripheral Vascular Disease 71 0.154
120
LYM133 Lymphoma, Hodgkin, Classic 69 0.154
121
P ADL017 Adult T-Cell Leukemia 56 0.154
122
P LPS004 Lupus Erythematosus 61 0.153
123
CRD132 Cardiac Conduction Defect 58 0.152
124
P BCL017 B-Cell Lymphoma 58 0.151
125
P MSC003 Muscular Atrophy 52 0.151
126
TXC005 Toxic Shock Syndrome 62 0.150
127
P MYC008 Myocarditis 59 0.149
128
P SYS005 Systemic Scleroderma 68 0.149
129
ART074 Aortic Dissection 52 0.149
130
P PHC003 Pheochromocytoma 71 0.149
131
P RSP003 Respiratory Failure 74 0.149
132
URT010 Ureteral Obstruction 45 0.149
133
SQM006 Squamous Cell Carcinoma 60 0.148
134
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.148
135
P BLD134 Bladder Cancer 79 0.148
136
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.147
137
P SLP006 Sleep Apnea 69 0.147
138
P GST053 Gastric Cancer 83 0.147
139
ADR040 Adrenal Gland Pheochromocytoma 46 0.146
140
c MCR129 Microvascular Complications of Diabetes 1 66 0.146
141
IMM167 Immune Deficiency Disease 78 0.146
142
DFC004 Deficiency Anemia 70 0.145
143
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.145
144
P OST002 Osteoporosis 74 0.145
145
P FML187 Familial Hypertension 37 0.145
146
P PRP019 Peripheral Nervous System Disease 58 0.144
147
P ART021 Arteriosclerosis 54 0.143
148
ATX019 Ataxia with Vitamin E Deficiency 42 0.143
149
IMP005 Impotence 52 0.142
150
c MLG069 Malignant Hypertension 47 0.142
151
PRT013 Portal Hypertension 59 0.142
152
INT007 Intermediate Coronary Syndrome 55 0.140
153
P UVT001 Uveitis 57 0.139
154
RCK004 Rickets 68 0.139
155
c MCR112 Microvascular Complications of Diabetes 2 41 0.139
156
47X002 47,xyy 49 0.139
157
MCS002 Mucositis 56 0.138
158
P PSR002 Psoriasis 62 0.138
159
ACQ007 Acquired Immunodeficiency Syndrome 60 0.137
160
PST011 Pustulosis of Palm and Sole 52 0.137
161
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.137
162
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.136
163
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.136
164
AGN016 Aging 56 0.136
165
P HYP069 Hyperparathyroidism 63 0.136
166
SKN019 Skin Melanoma 68 0.136
167
ANX010 Anxiety 73 0.135
168
P KDN017 Kidney Cancer 60 0.135
169
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.134
170
FTT001 Fatty Liver Disease 61 0.133
171
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.133
172
c MGR028 Migraine with or Without Aura 1 67 0.133
173
P PLY014 Polycystic Kidney Disease 62 0.133
174
PLM010 Pulmonary Edema 54 0.132
175
DPR016 Depression 63 0.132
176
P GRF003 Graft-Versus-Host Disease 72 0.131
177
P MSC005 Muscular Dystrophy 66 0.131
178
P LKM062 Leukemia, Acute Lymphoblastic 69 0.131
179
SRC014 Sarcoma 65 0.130
180
SPN035 Spindle Cell Sarcoma 53 0.130
181
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.130
182
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.130
183
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.130
184
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.130
185
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.130
186
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.130
187
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.130
188
THR024 Thrombosis 57 0.130
189
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.130
190
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.130
191
P GLM040 Glioma Susceptibility 1 81 0.129
192
OST012 Osteoarthritis 78 0.129
193
c ACT027 Acute Pancreatitis 60 0.129
194
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.129
195
STM007 Stomatitis 50 0.129
196
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.129
197
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.129
198
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.129
199
MYL009 Myelodysplastic Syndrome 70 0.128
200
ACR007 Acromegaly 71 0.127
201
OST159 Osteogenic Sarcoma 66 0.127
202
P LKM071 Leukemia, Chronic Lymphocytic 79 0.126
203
LNG031 Lung Benign Neoplasm 51 0.126
204
P PNM007 Pneumonia 68 0.125
205
GLC003 Glucose Intolerance 54 0.125
206
c THR092 Thrombophilia Due to Thrombin Defect 73 0.125
207
SYS003 Systolic Heart Failure 49 0.125
208
P RHM011 Rheumatoid Arthritis 80 0.123
209
PRT058 Pure Autonomic Failure 59 0.123
210
P CRD119 Cardiac Arrest 67 0.123
211
MNT002 Mental Depression 58 0.123
212
P FCL005 Focal Segmental Glomerulosclerosis 57 0.122
213
P INF038 Influenza 68 0.122
214
P HYP750 Hypertriglyceridemia, Familial 62 0.122
215
VCC001 Vaccinia 49 0.121
216
TTN003 Tetanus 65 0.121
217
c HPT001 Hepatitis C 62 0.121
218
P ALP008 Alopecia 54 0.121
219
CRB004 Cerebral Artery Occlusion 45 0.120
220
P ENC018 Encephalopathy 61 0.120
221
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.120
222
P MYP004 Myopathy 70 0.120
223
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.119
224
P HDC001 Headache 57 0.119
225
THY029 Thyroid Carcinoma 59 0.119
226
P LNG064 Lung Cancer Susceptibility 3 78 0.119
227
OVR094 Ovarian Epithelial Cancer 38 0.118
228
c RHB024 Rhabdomyosarcoma 2 67 0.118
229
HNS001 Hansen's Disease 34 0.118
230
HYP014 Hyperuricemia 52 0.118
231
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.118
232
P LPR021 Leprosy 3 69 0.118
233
SYN036 Syncope 45 0.117
234
P HRP006 Herpes Simplex 65 0.117
235
P HPT021 Hepatitis 67 0.117
236
SCH014 Schistosomiasis 57 0.117
237
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.117
238
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.116
239
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.116
240
NPH010 Nephrosclerosis 50 0.116
241
PNG002 Pain Agnosia 51 0.116
242
ALC007 Alcohol Dependence 66 0.116
243
P URT039 Urticaria 58 0.115
244
ESP021 Esophageal Cancer 90 0.115
245
P AST007 Astrocytoma 51 0.115
246
PLS009 Plasma Cell Neoplasm 51 0.115
247
BRN071 Brain Injury 49 0.115
248
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.115
249
P DBT005 Diabetes Insipidus 55 0.114
250
P ANT006 Antiphospholipid Syndrome 55 0.114
251
P PRD008 Periodontitis 64 0.114
252
SMN007 Seminoma 43 0.113
253
PRS045 Prostatic Hypertrophy 53 0.113
254
P ADL010 Adult Respiratory Distress Syndrome 65 0.113
255
PLM033 Pulmonary Embolism 59 0.112
256
P DMN002 Dementia 66 0.112
257
MRF001 Marfan Syndrome 77 0.112
258
P PLY011 Polycystic Ovary Syndrome 56 0.111
259
LYM027 Lymphopenia 58 0.111
260
CNS004 Constipation 58 0.111
262
SFT003 Soft Tissue Sarcoma 56 0.111
263
P GCH001 Gaucher's Disease 63 0.111
264
HRW001 Hair Whorl 36 0.110
265
c CHR064 Chronic Monocytic Leukemia 33 0.110
266
CRH001 Crohn's Disease 74 0.110
267
P INF032 Infertility 57 0.110
268
MDD011 Mood Disorder 62 0.109
269
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.108
270
SCH036 Scheie Syndrome 72 0.108
271
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.108
272
P SZR006 Seizure Disorder 56 0.108
273
P RCT021 Rectum Cancer 52 0.107
274
c MTR002 Mitral Valve Insufficiency 48 0.107
275
CLT003 Colitis 62 0.107
276
CRN030 Coronary Stenosis 50 0.107
277
SVR004 Severe Combined Immunodeficiency 73 0.107
278
BRN028 Brain Cancer 74 0.107
279
P ART022 Arthritis 69 0.107
280
TRM010 Traumatic Brain Injury 51 0.106
281
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.106
282
c HRD002 Hereditary Angioedema 60 0.106
283
LYM040 Lymphoblastic Lymphoma 54 0.106
284
c ACT073 Acute Leukemia 58 0.106
285
c PRS136 Prostate Cancer, Hereditary, 6 33 0.106
286
c PRS130 Prostate Cancer, Hereditary, 8 32 0.106
287
PRS021 Prostatic Adenoma 51 0.105
288
PLM012 Pulmonary Sarcoidosis 53 0.105
289
SKN016 Skin Disease 63 0.105
290
DRM006 Dermatitis 61 0.105
291
BRN024 Bronchitis 68 0.105
292
P PNC044 Pancreatitis 61 0.105
293
PRS129 Prostatic Hyperplasia, Benign 49 0.104
294
c LKM063 Leukemia, Chronic Myeloid 72 0.104
295
P MJR001 Major Depressive Disorder 68 0.104
296
DYS073 Dysphagia 50 0.104
297
P ALC033 Alcohol Use Disorder 58 0.103
298
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.103
299
P IGN003 Iga Nephropathy 1 49 0.103
300
HYP006 Hypertensive Heart Disease 49 0.103
301
NNL006 Non-Alcoholic Steatohepatitis 54 0.103
302
ALL014 Allergic Encephalomyelitis 38 0.103
303
HMT002 Hematologic Cancer 62 0.102
304
CRD223 Cardiac Arrhythmia 60 0.102
305
URM002 Uremia 49 0.101
306
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.101
307
ANR004 Anuria 46 0.101
308
PLM001 Pulmonary Tuberculosis 69 0.101
309
GLM044 Glomerular Disease 37 0.101
310
ALD013 Aldosterone-Producing Adenoma 39 0.101
311
VRL011 Viral Infectious Disease 61 0.100
312
HYD002 Hydronephrosis 60 0.100
313
SLC006 Silicosis 56 0.099
314
P MMB011 Membranous Nephropathy 50 0.099
315
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.099
316
ATN005 Autonomic Dysfunction 46 0.099
317
MSC157 Muscular Dystrophy, Duchenne Type 72 0.099
318
P MLG074 Malignant Mesenchymoma 40 0.099
319
P HYD006 Hydrocephalus 66 0.099
320
c VRL010 Viral Hepatitis 52 0.099
321
CHG001 Chagas Disease 66 0.098
322
CRV035 Cervical Cancer 76 0.098
323
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.098
324
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.098
325
VSL002 Visual Epilepsy 59 0.097
326
CYS001 Cystic Fibrosis 81 0.097
327
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.097
328
PRT036 Peritonitis 64 0.097
329
c PRM005 Primary Hyperparathyroidism 58 0.097
330
P ENC004 Encephalitis 61 0.096
331
P RHN004 Rhinitis 57 0.096
332
ANX004 Anoxia 40 0.096
333
PRP030 Purpura 54 0.096
334
P RTN024 Retinoblastoma 73 0.096
335
P VSC011 Vasculitis 62 0.096
336
c FML008 Familial Retinoblastoma 53 0.096
337
OLG003 Oligohydramnios 51 0.096
338
TRN015 Transient Cerebral Ischemia 63 0.096
339
P CNR004 Cone-Rod Dystrophy 2 73 0.096
340
CMP010 Complex Regional Pain Syndrome 58 0.096
341
c HPT073 Hepatitis C Virus 72 0.096
342
AST005 Asthma 76 0.095
343
P SCH015 Schizophrenia 74 0.095
344
DPH001 Diphtheria 60 0.095
345
P SKN015 Skin Carcinoma 66 0.095
346
CNN005 Connective Tissue Disease 68 0.095
347
P SYP003 Syphilis 58 0.095
348
PPL052 Papillomatosis, Confluent and Reticulated 33 0.095
349
SPN186 Spinal Cord Injury 60 0.095
350
VSC002 Vascular Dementia 57 0.094
351
PNC129 Pancreatic Adenocarcinoma 68 0.094
352
P CRC039 Coarctation of Aorta 47 0.094
353
P FLL037 Follicular Lymphoma 67 0.094
354
HMR039 Hemorrhage, Intracerebral 57 0.094
355
DBT010 Diabetic Neuropathy 54 0.094
356
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.093
357
P ART018 Aortic Valve Insufficiency 49 0.093
358
P ESP024 Esophagitis 62 0.093
359
PRP080 Peripheral Artery Disease 53 0.093
360
ULC004 Ulcerative Colitis 73 0.093
361
P INF037 Inflammatory Bowel Disease 54 0.093
362
c HPT016 Hepatitis B 59 0.093
363
P LTR001 Lateral Sclerosis 54 0.093
364
P CTR002 Cataract 60 0.093
365
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.093
366
ATS010 Autosomal Recessive Disease 48 0.092
367
MTB004 Metabolic Acidosis 50 0.092
368
P MLT020 Multiple Sclerosis 72 0.091
369
INT066 Interstitial Lung Disease 60 0.091
370
P GST044 Gastritis 56 0.091
371
NTR005 Nutritional Deficiency Disease 62 0.091
372
P OPT006 Optic Nerve Disease 60 0.090
373
P AMY004 Amyloidosis 70 0.090
374
P CHR345 Chronic Pain 44 0.090
375
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.090
376
P END044 Endometriosis 63 0.090
377
c OVR114 Ovarian Cancer 1 38 0.089
378
OCL069 Ocular Motor Apraxia 51 0.089
379
BCT022 Bacterial Infectious Disease 56 0.089
380
RTN020 Retinal Vascular Disease 46 0.089
381
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.089
382
GRN017 Granulocytopenia 44 0.089
383
PPT005 Peptic Ulcer Disease 59 0.088
384
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.088
385
MNT001 Mantle Cell Lymphoma 69 0.088
386
KPS004 Kaposi Sarcoma 75 0.088
387
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.088
388
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.088
389
SPL018 Splenomegaly 48 0.087
390
c ACT135 Acute Graft Versus Host Disease 52 0.087
391
P RTN018 Retinal Disease 53 0.087
392
c EXD008 Exudative Vitreoretinopathy 1 71 0.087
393
MLR004 Malaria 81 0.087
395
c ACT068 Acute Cystitis 63 0.087
396
GT001 Gout 64 0.086
397
P HYP098 Hypereosinophilic Syndrome 67 0.086
398
CNN003 Conn's Syndrome 79 0.086
399
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.086
400
ANR007 Anorexia Nervosa 63 0.086
401
c WLM018 Wilms Tumor 5 61 0.086
402
P GLY013 Glycogen Storage Disease 60 0.086
403
MSL001 Measles 62 0.086
404
HRT012 Heart Valve Disease 53 0.086
405
P MLT074 Multiple Endocrine Neoplasia 56 0.085
406
CHL065 Cholangiocarcinoma 68 0.085
407
FCT007 Factor Vii Deficiency 67 0.085
408
GST023 Gastric Ulcer 53 0.085
409
c VSC019 Vesicoureteral Reflux 1 57 0.085
410
P GRV001 Graves' Disease 55 0.084
411
P TRM003 Tremor 54 0.084
412
PST028 Post-Traumatic Stress Disorder 58 0.084
413
P PLY018 Polycythemia 56 0.084
414
P FBR017 Fibrosarcoma 56 0.084
415
BRK010 Burkitt Lymphoma 67 0.084
416
HRT011 Heart Septal Defect 50 0.084
417
P NSP012 Nasopharyngeal Carcinoma 66 0.084
418
GLS001 Gliosarcoma 54 0.084
419
c SPN225 Spondyloarthropathy 1 73 0.084
420
P PLY019 Polyneuropathy 56 0.084
421
c FLL041 Follicular Lymphoma 1 49 0.083
422
BRR014 Barrett Esophagus 65 0.083
423
P PYL005 Pyelonephritis 56 0.083
424
P SCK005 Sickle Cell Disease 50 0.083
425
P INS002 in Situ Carcinoma 53 0.083
426
P HYP120 Hypoaldosteronism 36 0.083
427
c BSL007 Basal Cell Carcinoma 68 0.083
428
ATR057 Atrioventricular Block 55 0.083
429
ACT084 Acute Stress Disorder 47 0.083
430
ALL003 Allergic Rhinitis 67 0.083
431
IRN002 Iron Metabolism Disease 57 0.082
432
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.082
433
DST006 Diastolic Heart Failure 45 0.082
434
P MTR003 Mitral Valve Stenosis 50 0.082
435
INT079 Intrahepatic Cholangiocarcinoma 51 0.082
436
ATN004 Autonomic Neuropathy 45 0.081
437
RHM028 Rheumatic Heart Disease 53 0.081
438
P PRK057 Parkinson Disease, Late-Onset 78 0.081
439
c BRN108 Branchiootic Syndrome 1 62 0.081
440
P MJR007 Major Affective Disorder 1 43 0.080
441
CHL068 Cholestasis 61 0.080
442
LMB062 Limb Ischemia 55 0.080
443
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.080
444
CRT013 Carotid Stenosis 50 0.080
445
P THY032 Thyroiditis 52 0.080
446
HYP114 Hypertensive Nephropathy 36 0.080
447
P SBS003 Substance Abuse 55 0.080
448
P BND020 Bone Disease 59 0.080
449
HML018 Homologous Wasting Disease 22 0.080
450
CHL079 Children's Interstitial Lung Disease 26 0.079
451
P RHB003 Rhabdomyosarcoma 63 0.079
452
c CHR682 Chronic Bilirubin Encephalopathy 39 0.079
453
OBS082 Obstructive Nephropathy 42 0.079
454
P DDN001 Duodenal Ulcer 52 0.079
455
DFF005 Diffuse Large B-Cell Lymphoma 55 0.079
456
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.079
457
ADR016 Adrenal Cortical Carcinoma 48 0.079
458
NWB001 Newborn Respiratory Distress Syndrome 58 0.079
459
PTT037 Pituitary Tumors 44 0.078
460
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.078
461
SNS003 Sensory Peripheral Neuropathy 54 0.078
462
P SPP010 Suppressor of Tumorigenicity 3 51 0.078
463
MCL006 Macular Retinal Edema 55 0.078
464
c FML035 Familial Hyperlipidemia 55 0.078
465
END040 Endogenous Depression 55 0.078
466
ADR004 Adrenal Cortical Adenocarcinoma 39 0.077
467
MSN001 Mesangial Proliferative Glomerulonephritis 45 0.077
468
P MTR012 Mitral Valve Disease 58 0.077
469
GTR002 Goiter 53 0.077
470
EYD002 Eye Disease 58 0.076
471
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.076
472
MMB001 Membranoproliferative Glomerulonephritis 55 0.076
473
LSH001 Leishmaniasis 63 0.076
474
P KLZ004 Kala-Azar 1 41 0.076
475
c FNC043 Fanconi Anemia, Complementation Group E 62 0.076
476
P MLN007 Male Infertility 55 0.076
477
TST014 Testicular Cancer 46 0.076
478
CRD137 Cardiogenic Shock 47 0.075
479
INT002 Intermittent Claudication 61 0.075
480
URN010 Urinary Tract Obstruction 55 0.075
481
P EHL001 Ehlers-Danlos Syndrome 58 0.075
482
c MJR003 Major Affective Disorder 6 33 0.075
483
c MJR006 Major Affective Disorder 5 33 0.075
484
P PNC025 Panic Disorder 53 0.075
485
OVR029 Ovarian Hyperstimulation Syndrome 64 0.074
486
c ART101 Aortic Valve Disease 2 65 0.074
487
P THL005 Thalassemia 60 0.074
488
P SNS001 Sensorineural Hearing Loss 60 0.074
489
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.074
490
P OVR082 Overgrowth Syndrome 50 0.074
491
RTN017 Retinal Detachment 61 0.074
492
c SVR005 Severe Pre-Eclampsia 50 0.073
493
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.073
494
PLC008 Placenta Disease 50 0.073
495
MCP033 Mucopolysaccharidoses 38 0.073
496
KLD004 Keloid Disorder 40 0.073
497
c PNS012 Paine Syndrome 61 0.073
498
ART002 Arts Syndrome 64 0.073
499
P HNT016 Huntington Disease 72 0.073
500
HMC014 Homocysteinemia 53 0.073
501
c SCN007 Secondary Hyperparathyroidism 51 0.073
502
END041 Endometrial Adenocarcinoma 63 0.073
503
RYN005 Raynaud Phenomenon 47 0.073
504
P RNL028 Renal Tubular Dysgenesis 51 0.073
505
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.072
506
AMN003 Amnestic Disorder 54 0.072
507
CHR074 Choriocarcinoma 47 0.072
508
EMB004 Embryonal Carcinoma 56 0.072
509
VRC005 Varicose Veins 60 0.072
510
P VNT002 Ventricular Septal Defect 60 0.072
511
SCK003 Sickle Cell Anemia 74 0.072
512
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.072
513
P ORT004 Orthostatic Intolerance 62 0.072
514
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 68 0.072
515
c WLM013 Wilms Tumor 1 65 0.072
516
P NRV007 Nervous System Disease 66 0.072
517
LYS002 Lysosomal Storage Disease 52 0.072
518
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.071
519
c MJR008 Major Affective Disorder 2 35 0.071
520
P EPL164 Epilepsy 71 0.071
521
SPN051 Spondylitis 51 0.071
522
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.071
523
c HPT003 Hepatitis a 62 0.071
524
P ACT105 Acute Mountain Sickness 52 0.071
525
APN008 Apnea, Obstructive Sleep 64 0.071
526
INS001 Insulinoma 60 0.071
527
c MJR023 Major Affective Disorder 7 33 0.071
528
c MJR004 Major Affective Disorder 4 28 0.071
529
P DRM053 Dermatitis, Atopic 66 0.071
530
INF009 Inflammatory Spondylopathy 31 0.071
531
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.071
532
SBC016 Subacute Delirium 44 0.070
533
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.070
534
MYC006 Mycosis Fungoides 66 0.070
535
DSS008 Disease of Mental Health 58 0.070
536
CNT047 Contact Dermatitis 58 0.070
537
P CTN015 Cutaneous T Cell Lymphoma 49 0.070
538
CYT008 Cytomegalovirus Infection 57 0.070
539
c FML021 Familial Hypercholesterolemia 66 0.070
540
GRM010 Germ Cells Tumors 34 0.070
541
IDP033 Idiopathic Edema 44 0.069
542
IGR001 Ige Responsiveness, Atopic 59 0.069
543
GST045 Gastroenteritis 59 0.069
544
GST033 Gestational Diabetes 61 0.069
545
PRC013 Pericarditis 54 0.069
546
c GRV008 Graves Disease 1 56 0.069
547
P TTR001 Tetralogy of Fallot 70 0.069
548
CRN322 Coronavirus Infectious Disease 40 0.069
549
c MNN043 Meningioma, Familial 74 0.069
550
BRN056 Bronchopulmonary Dysplasia 57 0.069
551
P PRM006 Primary Biliary Cirrhosis 62 0.068
552
MRG003 Marginal Zone B-Cell Lymphoma 52 0.068
553
SXL003 Sexual Disorder 47 0.068
554
P MNN013 Meningitis 66 0.068
555
MNN042 Meningioma, Radiation-Induced 62 0.068
556
BRN004 Brain Edema 56 0.068
557
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.068
558
SPN021 Spinal Meningioma 50 0.068
559
BCK006 Back Pain 42 0.068
560
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.068
561
P TRT010 Teratoma 52 0.068
562
P PMP001 Pemphigus 54 0.068
563
c FML001 Familial Atrial Fibrillation 65 0.068
564
P ART023 Arthropathy 62 0.068
565
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.068
566
P TRC086 Trichohepatoenteric Syndrome 1 62 0.067
567
ARG004 Argyria 27 0.067
568
P OPN001 Open-Angle Glaucoma 49 0.067
569
SCR001 Secretory Meningioma 41 0.067
570
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.067
571
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.067
572
SNG003 Single Ventricular Heart 30 0.067
573
PLY150 Polykaryocytosis Inducer 31 0.067
574
ETN001 Eating Disorder 60 0.067
575
P PRL003 Proliferative Glomerulonephritis 44 0.067
576
C1N001 C1 Inhibitor Deficiency 39 0.067
577
HYP540 Hypertension, Diastolic 40 0.066
578
ANG049 Angioedema Induced by Ace Inhibitors 40 0.066
579
P SLP005 Sleep Disorder 59 0.066
580
PSY004 Psychotic Disorder 67 0.066
581
PLS025 Plasmablastic Lymphoma 47 0.066
582
DSS009 Disseminated Intravascular Coagulation 57 0.066
583
KHL003 Kohlschutter-Tonz Syndrome 65 0.066
584
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.066
586
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.065
587
RDN001 Reading Disorder 40 0.065
588
P HML001 Hemolytic-Uremic Syndrome 53 0.065
589
HYP017 Hypophosphatemia 50 0.065
590
49X006 49, Xxxxy Syndrome 41 0.065
591
ALL006 Allergic Asthma 56 0.065
592
NRT001 Neurotic Disorder 53 0.065
593
NPH009 Nephrolithiasis 55 0.065
594
P SML001 Small Cell Carcinoma 52 0.065
595
c HNT011 Huntington Disease-Like 3 38 0.065
596
P HYP055 Hypoplastic Left Heart Syndrome 63 0.065
597
P PSD003 Pseudohypoaldosteronism 44 0.065
598
MLT157 Multiple System Atrophy 1 70 0.065
599
P END033 Endocarditis 57 0.064
600
HDG004 Hodgkin's Granuloma 23 0.064
601
HDG006 Hodgkin's Paragranuloma 22 0.064
602
P CHN012 Chondrosarcoma 56 0.064
603
c PCH010 Pachyonychia Congenita 3 44 0.064
604
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.064
605
DNT012 Dental Caries 53 0.064
606
P PRM002 Primary Hyperoxaluria 62 0.064
607
P ART005 Arteriovenous Malformation 65 0.064
608
BRC012 Brucellosis 64 0.064
609
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.064
610
AVN001 Avian Influenza 59 0.064
611
P PLY041 Polymyositis 57 0.064
612
c CHR417 Chronic Graft Versus Host Disease 57 0.064
613
LMY002 Leiomyoma 52 0.064
614
P ATS364 Autism 70 0.064
615
FNG017 Fungal Infectious Disease 53 0.064
616
ANT018 Anthracosis 48 0.063
617
CHC001 Chickenpox 60 0.063
618
ERY051 Erythroleukemia, Familial 56 0.063
619
TST043 Testicular Seminoma 35 0.063
620
P PNM006 Pneumoconiosis 56 0.063
621
P LCT001 Lactic Acidosis 51 0.063
622
P CLC063 Celiac Disease 1 66 0.063
623
P HYP265 Hypotonia 43 0.062
624
THY030 Thyroid Gland Disease 52 0.062
625
P PLM034 Pulmonary Emphysema 55 0.062
626
MTH009 Mouth Disease 56 0.062
627
P RRH023 Rare Hereditary Hemochromatosis 41 0.062
628
KWS002 Kawasaki Disease 65 0.062
629
ACT003 Acute Kidney Tubular Necrosis 45 0.062
630
P DRM010 Dermatomyositis 61 0.062
631
P MGR003 Migraine with Aura 52 0.061
632
HMS001 Hemosiderosis 54 0.061
633
IDP091 Idiopathic Nephrotic Syndrome 42 0.061
634
c DRR009 Diarrhea 6 46 0.061
635
EXT034 Extrinsic Allergic Alveolitis 58 0.061
636
HLC007 Helicobacter Pylori Infection 59 0.061
637
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.061
638
P LMY004 Leiomyosarcoma 63 0.061
639
HDN002 Head Injury 46 0.061
640
P MGR001 Migraine Without Aura 49 0.061
641
PNM008 Pneumothorax 56 0.061
642
P ALP004 Alport Syndrome 68 0.061
643
MDD018 Middle East Respiratory Syndrome 43 0.061
644
c PRD040 Periodontitis, Chronic 53 0.061
645
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.061
646
TRN018 Transitional Cell Carcinoma 56 0.060
647
c GLC092 Glaucoma, Primary Open Angle 62 0.060
648
HYP081 Hypolipoproteinemia 51 0.060
649
HYP457 Hypertrophic Scars 42 0.060
650
P CYS018 Cystitis 59 0.060
651
PSR001 Psoriatic Arthritis 61 0.060
652
c ATM022 Autoimmune Myocarditis 35 0.060
653
MYL005 Myelofibrosis 70 0.060
654
INT067 Interstitial Nephritis 48 0.060
655
c NRF023 Neurofibromatosis, Type Ii 80 0.060
656
ART017 Aortic Disease 49 0.059
657
CLF027 Cleft Palate, Isolated 64 0.059
658
PRP016 Paraplegia 52 0.059
659
HRP004 Herpes Zoster 60 0.059
660
GST092 Gastroesophageal Reflux 67 0.059
661
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.059
662
P THR015 Thrombophilia 51 0.059
663
c ART115 Aortic Valve Disease 1 75 0.058
664
P HML002 Hemolytic Anemia 63 0.058
665
HYP043 Hyperandrogenism 48 0.058
666
CRC021 Carcinosarcoma 62 0.058
667
ORL015 Oral Squamous Cell Carcinoma 43 0.058
668
KRT019 Keratitis, Hereditary 65 0.058
669
HST010 Histiocytosis 48 0.058
670
PLY001 Polycythemia Vera 69 0.058
671
SZR001 Sezary's Disease 60 0.058
672
RHM001 Rheumatic Fever 60 0.058
673
AZS001 Azoospermia 50 0.058
674
P LYM033 Lymphoproliferative Syndrome 59 0.057
675
P MNC007 Monocytic Leukemia 53 0.057
676
PNC001 Pancytopenia 54 0.057
677
CYT018 Cytochrome P450 2d6 Variant 27 0.057
678
P RNL007 Renal Tubular Acidosis 51 0.057
679
SCH012 Schizoaffective Disorder 50 0.057
680
GST040 Gastric Adenocarcinoma 70 0.057
681
HYP080 Hypogonadism 50 0.057
682
ASB001 Asbestosis 47 0.056
683
ASB003 Asbestos Intoxication 26 0.056
684
P TMP001 Temporal Lobe Epilepsy 50 0.056
685
MLG164 Malignant Epithelial Tumor of Ovary 26 0.056
686
P OBS001 Obstructive Jaundice 50 0.056
687
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.056
688
BRN002 Bronchiolitis 59 0.056
689
CRH005 Crohn's Colitis 53 0.056
690
P BRS044 Breast Adenocarcinoma 59 0.056
691
AMN001 Amenorrhea 54 0.056
692
DBT006 Diabetic Macular Edema 48 0.056
693
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.056
694
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.056
695
SPL004 Splenic Marginal Zone Lymphoma 51 0.056
696
FBR047 Fibromyalgia 58 0.056
697
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.056
698
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.056
699
IDP011 Idiopathic Interstitial Pneumonia 59 0.056
700
c PST041 Posterior Urethral Valves 41 0.055
701
CRN020 Coronary Restenosis 39 0.055
702
INF034 Infective Endocarditis 53 0.055
703
ART004 Aortic Atherosclerosis 47 0.055
704
P VNW001 Von Willebrand's Disease 65 0.055
705
P PRP029 Porphyria 62 0.055
706
CLR109 Colorectal Adenocarcinoma 51 0.055
707
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.055
708
FBR012 Fabry Disease 72 0.055
709
c INF071 Inflammatory Bowel Disease 1 67 0.055
710
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.055
711
OCL006 Ocular Hypertension 53 0.055
712
CYN002 Cyanosis, Transient Neonatal 45 0.055
713
MYC005 Myocardial Stunning 46 0.055
714
P ALP009 Alopecia Areata 60 0.054
715
ORL011 Oral Cancer 60 0.054
716
GST071 Gastrointestinal Carcinoma 47 0.054
717
HRY003 Hairy Cell Leukemia 55 0.054
718
CRT016 Carotid Artery Disease 52 0.054
719
P CHL066 Cholangitis 51 0.054
720
P BNC003 Bone Cancer 58 0.054
721
CLN015 Colon Adenocarcinoma 65 0.054
722
P HYP083 Hypopituitarism 53 0.054
723
ADR005 Adrenal Carcinoma 58 0.054
724
ASP007 Aspiration Pneumonia 48 0.054
725
THR123 Thrombotic Microangiopathy 36 0.054
726
P MYS005 Myositis 56 0.054
727
ADR008 Adrenal Adenoma 55 0.054
728
P PRC012 Pericardial Effusion 51 0.054
729
HMP001 Hemopericardium 48 0.054
730
ACT119 Acute Promyelocytic Leukemia 63 0.053
731
SPS057 Spasticity 45 0.053
732
HYP025 Hyperphosphatemia 48 0.053
733
ENT011 Enterocolitis 51 0.053
734
CKT002 Cakut 48 0.053
735
NRS005 Neurosarcoidosis 36 0.053
736
TBC004 Tobacco Addiction 64 0.053
737
INT075 Intracranial Hypertension 53 0.053
738
CRB086 Cerebral Aneurysms 40 0.053
739
PST092 Posttransplant Acute Limbic Encephalitis 29 0.053
740
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.053
741
P PTN014 Patent Ductus Arteriosus 1 60 0.052
742
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.052
743
DBT008 Diabetic Angiopathy 44 0.052
744
PRM329 Premature Aging 35 0.052
745
OST003 Osteonecrosis 61 0.052
746
CRY004 Cryoglobulinemia 48 0.052
747
P GND004 Gonadal Dysgenesis 48 0.052
748
SPR126 Superior Semicircular Canal Dehiscence 40 0.052
749
PLY100 Polyploidy 40 0.052
750
INT030 Intracranial Aneurysm 56 0.052
751
RSP007 Respiratory Distress Syndrome, Infant 30 0.052
752
c ATM011 Autoimmune Hepatitis 63 0.052
753
c HMG029 Hemoglobin Se Disease 39 0.052
754
CHR066 Chronic Fatigue Syndrome 61 0.051
755
c CNT015 Central Sleep Apnea 45 0.051
756
P APL001 Aplastic Anemia 74 0.051
757
GNG013 Gingivitis 59 0.051
758
P ATR005 Atrophic Gastritis 50 0.051
759
ALL010 Allergic Contact Dermatitis 56 0.051
760
ATM052 Autoimmune Disease 1 37 0.051
761
RST023 Resting Heart Rate, Variation in 41 0.051
762
c ACT134 Acute Liver Failure 56 0.051
763
KDN013 Kidney Hypertrophy 32 0.051
764
CRN017 Coronary Thrombosis 47 0.051
765
PLR008 Pleurisy 50 0.051
766
c TRC022 Tricuspid Valve Insufficiency 45 0.051
767
P HMN010 Hemangioma 61 0.051
768
URL001 Urolithiasis 45 0.050
769
STT001 Status Epilepticus 60 0.050
770
P MYC033 Myoclonus 46 0.050
771
P CRN037 Craniosynostosis 68 0.050
772
DMY004 Demyelinating Disease 52 0.050
773
NRT004 Neuritis 52 0.050
774
ACR041 Acromelic Frontonasal Dysostosis 52 0.050
775
LCH001 Leech Infestation 35 0.050
776
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.050
777
CRV045 Cervical Intraepithelial Neoplasia 39 0.050
778
CRT017 Cartilage Disease 54 0.050
779
HYP781 Hypoascorbemia 51 0.050
780
QDR001 Quadriplegia 48 0.050
781
VRC001 Varicocele 49 0.050
782
HPT004 Hepatic Coma 45 0.050
783
HPT022 Hepatoblastoma 56 0.050
784
c DPH024 Diaphragmatic Hernia, Congenital 63 0.050
785
HPT014 Hepatorenal Syndrome 50 0.050
786
P OTS001 Otosclerosis 49 0.050
787
SYN007 Synovitis 54 0.050
788
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.050
789
P SLM003 Salmonellosis 55 0.050
790
P TRC031 Trichorhinophalangeal Syndrome 40 0.050
791
PLC002 Plica Syndrome 36 0.049
792
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.049
793
PNC034 Pancreas Disease 48 0.049
794
DBT002 Diabetic Autonomic Neuropathy 41 0.049
795
P LRY044 Larynx Cancer 55 0.049
796
FDL002 Food Allergy 51 0.049
797
ADR041 Adrenal Cortical Adenoma 43 0.049
798
HYP264 Hypertonia 38 0.049
799
GLS018 Glass Syndrome 57 0.049
800
WST005 West Nile Virus 54 0.049
801
P LCH002 Lichen Planus 53 0.049
802
LKS001 Leukostasis 46 0.049
803
P PRC031 Preeclampsia/eclampsia 1 38 0.049
804
PRS063 Paresthesia 41 0.049
805
P MCR010 Microcephaly 59 0.048
806
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.048
807
c ACT076 Acute Myocarditis 46 0.048
808
HYP020 Hyperprolactinemia 64 0.048
809
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.048
810
GST050 Gastrointestinal System Disease 56 0.048
811
ILS001 Ileus 51 0.048
812
c CHR098 Chronic Pyelonephritis 38 0.048
813
HPT019 Hepatic Encephalopathy 60 0.048
814
LMY014 Leiomyoma, Uterine 56 0.048
815
P PTT006 Pituitary Adenoma 55 0.048
816
P RTN016 Retinal Degeneration 53 0.048
817
c PNC106 Pancreatic Agenesis 1 51 0.048
818
PRD004 Prediabetes Syndrome 47 0.048
819
PLC005 Placental Insufficiency 57 0.048
820
P TST021 Testicular Germ Cell Tumor 60 0.047
821
P SCK002 Sick Sinus Syndrome 55 0.047
822
IMM001 Immune-Complex Glomerulonephritis 40 0.047
823
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 0.047
824
FNT004 Fainting 30 0.047
825
LPT014 Leptin Deficiency or Dysfunction 74 0.047
826
GLC008 Glucose Metabolism Disease 40 0.047
827
YLL002 Yellow Fever 61 0.047
828
P GLL018 Gallbladder Cancer 57 0.047
829
THY122 Thyroid Gland Cancer 57 0.047
830
CRT015 Carotid Artery Occlusion 45 0.047
831
SKN013 Skin Benign Neoplasm 51 0.047
832
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.047
833
PPL001 Papillary Adenoma 44 0.047
834
ALB002 Albinism 46 0.047
835
c BTT014 Beta-Thalassemia 74 0.047
836
OST017 Osteomyelitis 64 0.047
837
LYM051 Lymphomatoid Granulomatosis 45 0.047
838
LNG108 Langerhans Cell Histiocytosis 58 0.047
839
ALC010 Alcoholic Cardiomyopathy 42 0.046
840
CYS013 Cystinuria 63 0.046
841
P CLL015 Collagen Disease 47 0.046
842
GNG012 Gingival Overgrowth 51 0.046
843
FBR032 Fibromuscular Dysplasia 48 0.046
844
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.046
845
CRV038 Cervical Squamous Cell Carcinoma 58 0.046
846
HST011 Histoplasmosis 55 0.046
847
P BRN022 Bronchiectasis 59 0.046
848
P INT070 Intestinal Obstruction 58 0.046
849
P AVS003 Avascular Necrosis 42 0.046
850
CMP040 Complement Component 4, Partial Deficiency of 33 0.046
851
P MVM001 Movement Disease 63 0.046
852
VSC003 Visceral Leishmaniasis 55 0.046
853
P TBR001 Tuberous Sclerosis 70 0.046
854
P HML033 Hemolytic Uremic Syndrome, Atypical 1 68 0.046
855
SCH003 Schizophreniform Disorder 56 0.046
856
c INF145 Infantile Liver Failure Syndrome 1 50 0.046
857
P LNG028 Long Qt Syndrome 66 0.046
858
MXD005 Mixed Connective Tissue Disease 58 0.046
859
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.046
860
P ATR010 Atrial Heart Septal Defect 60 0.045
861
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.045
862
c JVN010 Juvenile Rheumatoid Arthritis 64 0.045
863
c LKM070 Leukemia, Acute Monocytic 57 0.045
864
P ANT001 Anterolateral Myocardial Infarction 34 0.045
865
KHN001 Kuhnt-Junius Degeneration 47 0.045
866
ALK024 Alkuraya-Kucinskas Syndrome 51 0.045
867
SKL017 Skeletal Dysplasias 40 0.045
868
P TST026 Testicular Germ Cell Cancer 43 0.045
869
c HYP768 Hyperlipoproteinemia, Type I 67 0.045
870
c BSL024 Basal Cell Carcinoma 1 56 0.045
871
DXR001 Doxorubicin Induced Cardiomyopathy 33 0.045
872
MST020 Mast Cell Activation Syndrome 26 0.045
873
ESP002 Esophageal Varix 51 0.045
874
c HYP272 Hypercholesterolemia, Familial, 3 44 0.045
875
P BRT004 Bartter Disease 52 0.045
876
P MTR014 Motor Neuron Disease 65 0.044
877
CHK001 Chikungunya 57 0.044
878
APH002 Aphasia 57 0.044
879
CLR030 Clear Cell Renal Cell Carcinoma 53 0.044
880
TRT001 Teratocarcinoma 45 0.044
881
STT041 Stuttering 52 0.044
882
LPR001 Lepromatous Leprosy 50 0.044
883
NTR046 Neutrophil Migration 50 0.044
884
TNS005 Tonsillitis 57 0.044
885
RSP006 Respiratory System Disease 50 0.044
886
CRS001 Crescentic Glomerulonephritis 43 0.044
887
BLR013 Biliary Tract Cancer 42 0.044
888
c CLR017 Clear Cell Sarcoma 45 0.044
889
GST020 Gastric Antral Vascular Ectasia 41 0.044
890
HMT008 Hematuria, Benign Familial 56 0.044
892
DCT002 Ductal Carcinoma in Situ 59 0.043
893
NRG002 Neurogenic Bladder 55 0.043
894
CHR100 Chronic Ulcer of Skin 55 0.043
895
P VNS003 Venous Insufficiency 55 0.043
896
PPT001 Peptic Esophagitis 52 0.043
897
CNG506 Congenital Amyoplasia 27 0.043
898
c WLM011 Wilms Tumor 6 37 0.043
899
P CYS039 Cystic Kidney Disease 54 0.043
900
ECT026 Ectopic Pregnancy 50 0.043
901
CCN002 Cocaine Abuse 49 0.043
902
EBL001 Ebola Hemorrhagic Fever 49 0.043
903
RNL078 Renal Dysplasia 50 0.043
904
P CLS010 Cluster Headache 42 0.043
905
WLF001 Wolff-Parkinson-White Syndrome 66 0.043
906
P DST002 Distal Arthrogryposis 63 0.043
907
HYP034 Hypertensive Encephalopathy 46 0.043
908
P ESS003 Essential Thrombocythemia 68 0.043
909
P SJG008 Sjogren Syndrome 61 0.043
910
SPP011 Suppression of Tumorigenicity 12 59 0.043
911
OVR112 Ovarian Germ Cell Cancer 45 0.043
912
CHL149 Childhood Acute Myeloid Leukemia 44 0.043
913
ALC009 Alcoholic Liver Cirrhosis 53 0.043
914
P GLL022 Guillain-Barre Syndrome 59 0.043
915
GSG001 Gas Gangrene 53 0.043
916
c ALP101 Alpha-Thalassemia 62 0.043
917
P OCL002 Oculocutaneous Albinism 60 0.043
918
BRN012 Bronchiolitis Obliterans 55 0.043
919
HSH003 Hashimoto Thyroiditis 62 0.043
920
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.043
921
IRD001 Iridocyclitis 53 0.042
922
MCR011 Microinvasive Gastric Cancer 43 0.042
923
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.042
924
PRS042 Prostate Disease 43 0.042
925
c HRD202 Hereditary Lymphedema I 50 0.042
926
THY125 Thyroid Gland Medullary Carcinoma 50 0.042
927
c CNG006 Congenital Hypothyroidism 64 0.042
928
THY111 Thyroid Carcinoma, Familial Medullary 67 0.042
929
IRR002 Irritable Bowel Syndrome 65 0.042
930
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.042
931
ING001 Inguinal Hernia 60 0.042
932
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.042
933
URT049 Urate Oxidase, Pseudogene 25 0.042
934
CRN019 Coronary Artery Vasospasm 46 0.042
935
c PRG020 Paragangliomas 3 39 0.042
936
NRM001 Neuromyelitis Optica 61 0.042
937
P PLY017 Polyarteritis Nodosa 58 0.042
938
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.042
939
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.042
940
CMP004 Complement Factor I Deficiency 44 0.042
941
P END084 Endocrine System Disease 45 0.041
942
P RTN022 Retinal Vein Occlusion 53 0.041
943
ACT029 Acute Interstitial Pneumonia 49 0.041
944
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.041
945
c VRL005 Viral Pneumonia 52 0.041
946
OVR063 Overnutrition 44 0.041
947
CRD016 Cardiac Rupture 37 0.041
948
SLP001 Sleeping Sickness 54 0.041
949
ONC002 Onchocerciasis 52 0.041
950
TRP009 Triple X Syndrome 42 0.041
951
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.041
952
PMP006 Pemphigus Vulgaris, Familial 57 0.041
953
HYD038 Hydrops Fetalis, Nonimmune 62 0.041
954
P OVR049 Ovarian Disease 52 0.041
955
HMP005 Hemiplegia 55 0.041
956
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 0.041
957
CCN001 Cocaine Dependence 48 0.041
958
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.041
959
c ANG068 Angioedema, Hereditary, Type I 57 0.041
960
HNC001 Henoch-Schoenlein Purpura 55 0.040
961
RNL097 Renal Artery Disease 42 0.040
962
c MCL013 Mucolipidosis Iv 66 0.040
963
PLY012 Polyhydramnios 46 0.040
964
PST053 Postherpetic Neuralgia 40 0.040
965
MCL003 Macular Holes 40 0.040
966
FCL012 Facial Paralysis 46 0.040
967
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.040
968
P OCL013 Oculodentodigital Dysplasia 69 0.040
969
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 46 0.040
970
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.040
971
MSC152 Muscular Dystrophy, Becker Type 63 0.040
972
IMM136 Immune System Disease 45 0.040
973
CLS052 Classic Hairy Cell Leukemia 27 0.040
974
APP008 Appendicitis 61 0.040
975
P RST002 Restrictive Cardiomyopathy 56 0.040
976
c BCT013 Bacterial Pneumonia 48 0.040
977
GTL001 Gitelman Syndrome 65 0.039
978
PST048 Postural Orthostatic Tachycardia Syndrome 45 0.039
979
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 0.039
980
c ACQ012 Acquired Angioedema 38 0.039
981
BRS099 Breast Ductal Carcinoma 62 0.039
982
CCC001 Coccidioidomycosis 58 0.039
983
c DWL002 Dowling-Degos Disease 1 58 0.039
984
LST001 Listeriosis 56 0.039
985
ACT200 Acute Monoblastic Leukemia 52 0.039
986
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.039
987
P CHR012 Chronic Granulomatous Disease 67 0.039
988
P OPT009 Optic Neuritis 57 0.039
989
PLR007 Pleural Empyema 50 0.039
990
END062 Endometrial Hyperplasia 48 0.039
991
SYS071 Systemic Autoimmune Disease 37 0.039
992
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.039
993
P LMB006 Limb-Girdle Muscular Dystrophy 53 0.039
994
c FCL025 Focal Segmental Glomerulosclerosis 1 46 0.039
995
BRS051 Breast Disease 58 0.039
996
c SYS043 Systemic Lupus Erythematosus 1 38 0.039
997
PRS047 Prostatitis 56 0.039
998
ANV001 Anovulation 47 0.039
999
c MCR256 Microphthalmia, Syndromic 9 56 0.039
1000
PRT029 Parathyroid Adenoma 50 0.039
1001
DRG024 Drug Allergy 42 0.039
1002
P DST107 Distal Renal Tubular Acidosis 42 0.039
1003
CHL004 Cholelithiasis 49 0.039
1004
KRT002 Keratomalacia 47 0.039
1005
P END039 Endodermal Sinus Tumor 44 0.039
1006
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 62 0.039
1007
END021 Endomyocardial Fibrosis 49 0.039
1008
HYP008 Hypertensive Retinopathy 39 0.039
1009
c PSD114 Pseudohypoaldosteronism, Type I, Autosomal Recessive 59 0.038
1010
MNN020 Meningococcal Infection 46 0.038
1011
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.038
1012
c PRG126 Progressive Familial Heart Block 55 0.038
1013
GST037 Gastroparesis 54 0.038
1014
P SCL009 Sclerosing Cholangitis 48 0.038
1015
PRT011 Protein C Deficiency 44 0.038
1016
CHR073 Choreatic Disease 52 0.038
1017
MRD002 Marden-Walker Syndrome 56 0.038
1018
PGM001 Pigmented Villonodular Synovitis 56 0.038
1019
HMG002 Hemoglobinuria 50 0.038
1020
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.038
1021
c CHL119 Cholangitis, Primary Sclerosing 57 0.038
1022
P SHR001 Short Bowel Syndrome 53 0.038
1023
MSM014 Mismatch Repair Cancer Syndrome 65 0.038
1024
P HMC002 Homocystinuria 53 0.038
1025
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.038
1026
KWS001 Kwashiorkor 44 0.038
1027
GRM004 Germinoma 40 0.038
1028
c ALM001 Al Amyloidosis 50 0.037
1029
AGR002 Agoraphobia 45 0.037
1030
TST018 Testicular Yolk Sac Tumor 39 0.037
1031
c TST046 Testicular Germ Cell Tumor 1 29 0.037
1032
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.037
1033
SBC001 Subacute Sclerosing Panencephalitis 56 0.037
1034
TRD006 Tardive Dyskinesia 54 0.037
1035
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.037
1036
c PRM196 Premature Ovarian Failure 1 67 0.037
1037
P HYP838 Hyperlipidemia, Familial Combined, 3 56 0.037
1038
P PRD021 Periodic Paralysis 45 0.037
1039
c VRL007 Viral Encephalitis 51 0.037
1040
PRC003 Proctitis 47 0.037
1041
NSS002 Neisseria Meningitidis Infection 47 0.037
1042
P MTH007 Methemoglobinemia 46 0.037
1043
P TMP003 Temporal Arteritis 68 0.037
1044
DFF035 Diffuse Cutaneous Systemic Sclerosis 49 0.037
1045
GYN001 Gynecomastia 49 0.037
1046
RFR002 Refractory Hairy Cell Leukemia 33 0.037
1047
P FML018 Familial Mediterranean Fever 73 0.036
1048
P SCL048 Sclerosteosis 55 0.036
1049
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.036
1050
LPT006 Leptin Receptor Deficiency 48 0.036
1051
c BCT007 Bacterial Meningitis 55 0.036
1052
NPH003 Nephrocalcinosis 51 0.036
1053
c GLY008 Glycogen Storage Disease Ii 70 0.036
1054
FML037 Female Breast Cancer 52 0.036
1055
LFT001 Left Bundle Branch Hemiblock 49 0.036
1056
PLC007 Placental Abruption 48 0.036
1057
INF021 Infant Gynecomastia 31 0.036
1058
ADR007 Adrenoleukodystrophy 75 0.036
1059
WLS001 Wilson Disease 71 0.036
1060
CLR108 Colorectal Adenoma 64 0.036
1061
PRT014 Protein S Deficiency 44 0.036
1062
TTR011 Tetraploidy 47 0.036
1063
c PRM093 Premature Ovarian Failure 7 47 0.036
1064
HYP344 Hyperthyroidism, Familial Gestational 39 0.036
1065
PTT046 Pituitary Hormone Deficiency, Combined, 2 64 0.036
1066
TNG009 Tongue Squamous Cell Carcinoma 44 0.036
1067
PMP004 Pemphigus Foliaceus 43 0.036
1068
P FML011 Familial Adenomatous Polyposis 72 0.035
1069
c LCL006 Localized Scleroderma 62 0.035
1070
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.035
1071
c TBR025 Tuberous Sclerosis 1 77 0.035
1072
P LRY019 Laryngitis 52 0.035