Search results for 5(S)-Hydroperoxyeicosatetraenoic acid

2528 hits were found for 5(S)-Hydroperoxyeicosatetraenoic acid

# Family MCID Name MIFTS Score
1
P LVR013 Liver Disease 68 0.342
2
HLX001 Helix Syndrome 47 0.324
3
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.323
4
P CLR023 Colorectal Cancer 99 0.320
5
P NRB001 Neuroblastoma 72 0.309
6
P DRR001 Diarrhea 55 0.299
7
P BRS047 Breast Cancer 97 0.295
8
48X005 48,xyyy 39 0.294
9
P KDN018 Kidney Disease 72 0.289
10
LVR012 Liver Cirrhosis 62 0.283
11
FTT001 Fatty Liver Disease 61 0.268
12
CHL068 Cholestasis 61 0.264
13
P LKM002 Leukemia 68 0.251
14
P HPT023 Hepatocellular Carcinoma 100 0.251
15
PRT037 Pertussis 65 0.249
16
OST012 Osteoarthritis 78 0.246
17
P GLM045 Glioma 63 0.241
18
P PRS040 Prostate Cancer 97 0.239
19
P MYL006 Myeloid Leukemia 60 0.237
20
GLL048 Glial Tumor 45 0.237
21
HMN044 Human Immunodeficiency Virus Type 1 71 0.235
22
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.234
23
P SZR006 Seizure Disorder 56 0.233
24
P ADN016 Adenocarcinoma 64 0.232
25
ISC004 Ischemia 58 0.232
26
P ALZ034 Alzheimer Disease 88 0.228
27
P HRP006 Herpes Simplex 65 0.227
28
P LNG032 Lung Cancer 98 0.227
29
P BLD134 Bladder Cancer 79 0.225
30
ATM095 Autoimmune Disease 62 0.224
31
VSL002 Visual Epilepsy 59 0.224
32
P OVR042 Ovarian Cancer 88 0.222
33
c CHR684 Chronic Kidney Disease 70 0.221
34
c HYP595 Hypertension, Essential 84 0.219
35
DPR016 Depression 63 0.217
36
CHL014 Cholera 59 0.216
37
ALL026 Allergic Hypersensitivity Disease 62 0.216
38
P INF037 Inflammatory Bowel Disease 54 0.215
39
ACT119 Acute Promyelocytic Leukemia 63 0.214
40
LPD008 Lipid Metabolism Disorder 62 0.214
41
HRW001 Hair Whorl 36 0.213
42
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.213
43
P CRN300 Coronary Heart Disease 1 63 0.213
44
c THR092 Thrombophilia Due to Thrombin Defect 73 0.211
45
ADN018 Adenoma 59 0.211
46
c LKM061 Leukemia, Acute Myeloid 84 0.210
47
DRM006 Dermatitis 61 0.210
48
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.209
49
PRT014 Protein S Deficiency 44 0.209
50
BNR002 Bone Resorption Disease 48 0.209
51
c NRF023 Neurofibromatosis, Type Ii 80 0.207
52
GLB015 Glioblastoma Multiforme 75 0.207
53
P VSC007 Vascular Disease 63 0.207
54
HYP066 Hyperglycemia 61 0.206
55
c HPT073 Hepatitis C Virus 72 0.205
56
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.205
57
47X002 47,xyy 49 0.204
58
DFC004 Deficiency Anemia 70 0.203
59
NRL016 Neural Tube Defects 82 0.202
60
HYP056 Hypoglycemia 66 0.201
61
LPP008 Lipoprotein Quantitative Trait Locus 62 0.201
62
GST092 Gastroesophageal Reflux 67 0.200
63
MNT002 Mental Depression 58 0.200
64
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.200
65
ULC004 Ulcerative Colitis 73 0.200
66
HYP014 Hyperuricemia 52 0.199
67
ATH013 Atherosclerosis Susceptibility 65 0.199
68
P DBT009 Diabetes Mellitus 64 0.199
69
P PNC035 Pancreatic Cancer 84 0.199
70
CLT003 Colitis 62 0.198
71
P LYM118 Lymphoma 68 0.197
72
P PSR002 Psoriasis 62 0.197
73
LNG099 Lung Disease 60 0.197
74
P GST053 Gastric Cancer 83 0.195
75
PST011 Pustulosis of Palm and Sole 52 0.194
76
CRH001 Crohn's Disease 74 0.193
77
CYS001 Cystic Fibrosis 81 0.192
78
c HPT016 Hepatitis B 59 0.192
79
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.191
80
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.190
81
MTB004 Metabolic Acidosis 50 0.189
82
VCC001 Vaccinia 49 0.188
83
P ENC018 Encephalopathy 61 0.187
84
P NTR004 Neutropenia 63 0.187
85
THR024 Thrombosis 57 0.186
86
c PRC016 Pre-Eclampsia 63 0.186
87
P NRP001 Neuropathy 56 0.186
88
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.186
89
P DDN001 Duodenal Ulcer 52 0.186
90
c HYP836 Hypercholesterolemia, Familial, 1 73 0.186
91
P THL005 Thalassemia 60 0.185
92
P HRT032 Heart Disease 75 0.184
93
SQM006 Squamous Cell Carcinoma 60 0.184
94
OST159 Osteogenic Sarcoma 66 0.183
95
P TRN020 Turner Syndrome 67 0.183
96
P OST002 Osteoporosis 74 0.182
97
SCH014 Schistosomiasis 57 0.182
98
BRR014 Barrett Esophagus 65 0.181
99
DWN001 Down Syndrome 70 0.181
100
ART140 Arteries, Anomalies of 52 0.181
101
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.181
102
CYT002 Cytokine Deficiency 42 0.180
103
GT001 Gout 64 0.178
104
LYM133 Lymphoma, Hodgkin, Classic 69 0.178
105
P RTN024 Retinoblastoma 73 0.178
106
P HNT016 Huntington Disease 72 0.177
107
c FML008 Familial Retinoblastoma 53 0.176
108
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.175
109
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.175
110
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.173
111
GST045 Gastroenteritis 59 0.173
112
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.173
113
PRS045 Prostatic Hypertrophy 53 0.173
114
P CTR002 Cataract 60 0.172
115
PLM001 Pulmonary Tuberculosis 69 0.172
116
P MJR001 Major Depressive Disorder 68 0.172
117
P HYP750 Hypertriglyceridemia, Familial 62 0.172
118
STM007 Stomatitis 50 0.172
119
SKN016 Skin Disease 63 0.172
120
c SYS001 Systemic Lupus Erythematosus 86 0.172
121
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.171
122
HMP009 Haemophilus Influenzae 43 0.171
123
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.171
124
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.171
125
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.171
126
MYL069 Myeloma, Multiple 85 0.170
127
CNG034 Congestive Heart Failure 69 0.168
128
P PRM006 Primary Biliary Cirrhosis 62 0.168
129
ADL002 Adult Syndrome 70 0.168
130
P LKM062 Leukemia, Acute Lymphoblastic 69 0.168
131
END086 End Stage Renal Disease 51 0.168
132
BCT022 Bacterial Infectious Disease 56 0.167
133
P MYC007 Myocardial Infarction 70 0.165
134
CRV035 Cervical Cancer 76 0.165
135
DNT012 Dental Caries 53 0.165
136
P BPL003 Bipolar Disorder 56 0.164
137
CRB039 Cerebrovascular Disease 67 0.164
138
P HYP086 Hypothyroidism 69 0.164
139
ALC007 Alcohol Dependence 66 0.163
140
c MJR024 Major Affective Disorder 9 41 0.162
141
c MJR022 Major Affective Disorder 8 38 0.162
142
HMC014 Homocysteinemia 53 0.161
143
PPT005 Peptic Ulcer Disease 59 0.161
144
c RHB024 Rhabdomyosarcoma 2 67 0.161
145
PRS021 Prostatic Adenoma 51 0.161
146
c SVR001 Severe Acute Respiratory Syndrome 62 0.161
147
MYL009 Myelodysplastic Syndrome 70 0.161
148
STR067 Stroke, Ischemic 81 0.160
149
P DRM053 Dermatitis, Atopic 66 0.160
150
P ESP024 Esophagitis 62 0.160
151
IMP005 Impotence 52 0.159
152
P MYP004 Myopathy 70 0.159
153
PNG002 Pain Agnosia 51 0.159
154
P BCL017 B-Cell Lymphoma 58 0.159
155
P GST044 Gastritis 56 0.159
156
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.158
157
P SCK005 Sickle Cell Disease 50 0.158
158
IRN002 Iron Metabolism Disease 57 0.158
159
IMM167 Immune Deficiency Disease 78 0.158
160
c GLL024 Gallbladder Disease 1 53 0.158
161
PRS129 Prostatic Hyperplasia, Benign 49 0.158
162
INS024 Insulin-Like Growth Factor I 79 0.158
163
c SML038 Small Cell Cancer of the Lung 65 0.157
164
c PCH010 Pachyonychia Congenita 3 44 0.157
165
P MLN008 Melanoma 69 0.157
166
AST005 Asthma 76 0.156
167
P MNN013 Meningitis 66 0.156
168
SRC014 Sarcoma 65 0.156
169
P HPT021 Hepatitis 67 0.155
170
SPN035 Spindle Cell Sarcoma 53 0.155
171
P CRD246 Cardiovascular System Disease 57 0.155
172
NTR005 Nutritional Deficiency Disease 62 0.155
173
PLM033 Pulmonary Embolism 59 0.154
174
P RHM011 Rheumatoid Arthritis 80 0.154
175
P THR014 Thrombocytopenia 67 0.154
176
THY029 Thyroid Carcinoma 59 0.154
177
NNL006 Non-Alcoholic Steatohepatitis 54 0.153
178
TXC005 Toxic Shock Syndrome 62 0.153
179
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.153
180
TRM010 Traumatic Brain Injury 51 0.153
181
c HPT001 Hepatitis C 62 0.153
182
P PRD008 Periodontitis 64 0.153
183
BRN071 Brain Injury 49 0.152
184
P ATS364 Autism 70 0.151
185
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.151
186
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.151
187
P ENC004 Encephalitis 61 0.150
188
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.150
189
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.150
190
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.150
191
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.150
192
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.150
193
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.150
194
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.150
195
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.150
196
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.150
197
PRT036 Peritonitis 64 0.150
198
P LTR001 Lateral Sclerosis 54 0.150
199
PPL052 Papillomatosis, Confluent and Reticulated 33 0.150
200
OCL069 Ocular Motor Apraxia 51 0.150
201
ANX010 Anxiety 73 0.150
202
P ART022 Arthritis 69 0.149
203
BRK010 Burkitt Lymphoma 67 0.149
204
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.149
205
MLR004 Malaria 81 0.147
206
KRT009 Keratosis 51 0.147
207
c MCR120 Microvascular Complications of Diabetes 7 47 0.147
208
c MCR113 Microvascular Complications of Diabetes 3 52 0.147
209
BRN024 Bronchitis 68 0.147
210
P SKN015 Skin Carcinoma 66 0.146
211
c MCR130 Microvascular Complications of Diabetes 6 41 0.146
212
c MCR133 Microvascular Complications of Diabetes 4 41 0.146
213
c ACT075 Acute Myocardial Infarction 57 0.146
214
P LPS004 Lupus Erythematosus 61 0.146
215
P CHR345 Chronic Pain 44 0.146
216
SCK003 Sickle Cell Anemia 74 0.146
217
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.146
218
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.145
219
ATX019 Ataxia with Vitamin E Deficiency 42 0.145
220
P PNM007 Pneumonia 68 0.145
221
P PRK057 Parkinson Disease, Late-Onset 78 0.145
222
c MGR028 Migraine with or Without Aura 1 67 0.144
223
SPN186 Spinal Cord Injury 60 0.144
224
HYP060 Hyperinsulinism 54 0.143
225
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.143
226
P UVT001 Uveitis 57 0.143
227
TTN003 Tetanus 65 0.142
228
P TRM003 Tremor 54 0.141
229
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.141
230
c ACT071 Acute Kidney Failure 60 0.141
231
TLN003 Telangiectasis 52 0.141
232
P SCH015 Schizophrenia 74 0.141
233
P INF032 Infertility 57 0.140
234
ESP021 Esophageal Cancer 90 0.140
235
P PLM037 Pulmonary Hypertension 67 0.140
236
GST023 Gastric Ulcer 53 0.140
237
c ATS007 Autism Spectrum Disorder 67 0.140
238
P CHL066 Cholangitis 51 0.140
239
SVR004 Severe Combined Immunodeficiency 73 0.139
240
P ATX030 Ataxia-Telangiectasia 82 0.139
241
c ACT068 Acute Cystitis 63 0.139
242
P INF038 Influenza 68 0.138
243
PRP030 Purpura 54 0.138
244
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.138
245
P RHN004 Rhinitis 57 0.138
246
ANG054 Angina Pectoris 66 0.137
247
AGN016 Aging 56 0.137
248
P HYP098 Hypereosinophilic Syndrome 67 0.137
249
RCK004 Rickets 68 0.136
250
P BND020 Bone Disease 59 0.136
251
c PNS012 Paine Syndrome 61 0.136
252
P PRP019 Peripheral Nervous System Disease 58 0.135
253
c ACT073 Acute Leukemia 58 0.135
254
ACQ007 Acquired Immunodeficiency Syndrome 60 0.135
255
c BSL007 Basal Cell Carcinoma 68 0.135
256
P GLM007 Glomerulonephritis 57 0.135
257
P EPL164 Epilepsy 71 0.134
258
P AST007 Astrocytoma 51 0.134
259
c ACT027 Acute Pancreatitis 60 0.134
260
CRB004 Cerebral Artery Occlusion 45 0.134
261
P MCR115 Microvascular Complications of Diabetes 5 66 0.133
262
P PHC003 Pheochromocytoma 71 0.133
263
P MSC005 Muscular Dystrophy 66 0.133
264
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.132
265
P RSP003 Respiratory Failure 74 0.132
266
P DMN002 Dementia 66 0.132
267
MST005 Mastitis 53 0.132
268
PPL022 Papilloma 54 0.131
269
DPH001 Diphtheria 60 0.131
270
P LKM071 Leukemia, Chronic Lymphocytic 79 0.131
271
EWN003 Ewing Sarcoma 69 0.131
272
P FBR017 Fibrosarcoma 56 0.131
273
ADR040 Adrenal Gland Pheochromocytoma 46 0.130
274
c DBT099 Diabetes Mellitus, Type I 65 0.130
275
PHN003 Phenylketonuria 75 0.130
276
STT001 Status Epilepticus 60 0.130
277
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.130
278
HPT004 Hepatic Coma 45 0.129
279
TYP007 Typhoid Fever 63 0.129
280
P END033 Endocarditis 57 0.129
282
P EXN002 Exanthem 57 0.128
283
c BTT014 Beta-Thalassemia 74 0.128
284
P ALP008 Alopecia 54 0.128
285
HYP005 Hypokalemia 55 0.128
286
URM002 Uremia 49 0.127
287
HNS001 Hansen's Disease 34 0.126
288
END057 Endometrial Cancer 74 0.126
289
ANX004 Anoxia 40 0.126
290
ORL011 Oral Cancer 60 0.126
291
LYM019 Lymphosarcoma 46 0.126
292
SQM002 Squamous Cell Papilloma 46 0.125
293
GLC003 Glucose Intolerance 54 0.125
294
P HYP076 Hyperthyroidism 55 0.125
295
P LPR021 Leprosy 3 69 0.124
296
c LKM063 Leukemia, Chronic Myeloid 72 0.124
297
P OVR082 Overgrowth Syndrome 50 0.124
298
P SCL018 Scoliosis 60 0.124
299
EMB004 Embryonal Carcinoma 56 0.124
300
CHC001 Chickenpox 60 0.124
301
P MSC003 Muscular Atrophy 52 0.124
302
P MLT020 Multiple Sclerosis 72 0.124
303
ALL014 Allergic Encephalomyelitis 38 0.124
304
P CRD119 Cardiac Arrest 67 0.124
305
P HDC001 Headache 57 0.123
306
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.123
307
CHL079 Children's Interstitial Lung Disease 26 0.123
308
P PNC044 Pancreatitis 61 0.123
309
RTN023 Retinitis 46 0.123
310
NRR001 Neuroretinitis 42 0.123
311
CNS004 Constipation 58 0.122
312
P HYP069 Hyperparathyroidism 63 0.122
313
P LNG064 Lung Cancer Susceptibility 3 78 0.122
314
CRD132 Cardiac Conduction Defect 58 0.122
315
P ALC033 Alcohol Use Disorder 58 0.122
316
P ECL001 Eclampsia 50 0.122
317
P PLM036 Pulmonary Fibrosis 65 0.122
318
c HPT003 Hepatitis a 62 0.122
319
CHL123 Chlamydia 59 0.121
320
P END044 Endometriosis 63 0.120
321
CLN015 Colon Adenocarcinoma 65 0.120
322
PLM010 Pulmonary Edema 54 0.120
323
P NPH012 Nephrotic Syndrome 60 0.119
324
c FNC043 Fanconi Anemia, Complementation Group E 62 0.119
325
MSL001 Measles 62 0.119
326
c ATR087 Atrial Standstill 1 75 0.119
327
c VRL010 Viral Hepatitis 52 0.119
328
c PRM038 Primary Agammaglobulinemia 44 0.119
329
OST003 Osteonecrosis 61 0.118
330
HPT019 Hepatic Encephalopathy 60 0.118
331
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.118
332
P ART021 Arteriosclerosis 54 0.117
333
c SPN225 Spondyloarthropathy 1 73 0.117
334
ERY051 Erythroleukemia, Familial 56 0.117
335
P CYS018 Cystitis 59 0.116
336
MDD011 Mood Disorder 62 0.116
337
ANR007 Anorexia Nervosa 63 0.116
338
CLF027 Cleft Palate, Isolated 64 0.116
339
P ACT008 Actinic Keratosis 53 0.116
340
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.115
341
P SLM003 Salmonellosis 55 0.115
342
ALL003 Allergic Rhinitis 67 0.115
343
MTH009 Mouth Disease 56 0.115
344
P ATR011 Atrial Fibrillation 66 0.115
345
ATS010 Autosomal Recessive Disease 48 0.115
346
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.114
347
P THR015 Thrombophilia 51 0.114
348
P KLZ004 Kala-Azar 1 41 0.114
349
LSH001 Leishmaniasis 63 0.114
350
c DWL002 Dowling-Degos Disease 1 58 0.114
351
P NSP012 Nasopharyngeal Carcinoma 66 0.114
352
P PLY019 Polyneuropathy 56 0.113
353
HMG005 Hemoglobinopathy 56 0.113
354
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.113
355
P RCT021 Rectum Cancer 52 0.113
356
OTT002 Otitis Media 72 0.113
357
NPH009 Nephrolithiasis 55 0.113
358
END040 Endogenous Depression 55 0.112
359
P INS002 in Situ Carcinoma 53 0.112
360
P VSC011 Vasculitis 62 0.112
361
EYD002 Eye Disease 58 0.112
362
HYP781 Hypoascorbemia 51 0.112
363
P TRC086 Trichohepatoenteric Syndrome 1 62 0.112
364
P SPP010 Suppressor of Tumorigenicity 3 51 0.111
365
CHL065 Cholangiocarcinoma 68 0.111
366
P HML002 Hemolytic Anemia 63 0.111
367
P RTN008 Retinitis Pigmentosa 79 0.111
368
GST033 Gestational Diabetes 61 0.111
369
ANR040 Aneurysm 59 0.111
370
MCS002 Mucositis 56 0.110
371
HLC007 Helicobacter Pylori Infection 59 0.110
372
c MLG068 Malignant Glioma 46 0.110
373
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.110
374
PLM031 Poliomyelitis 64 0.110
375
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.110
376
P KDN017 Kidney Cancer 60 0.110
377
DSS009 Disseminated Intravascular Coagulation 57 0.109
378
P PRP029 Porphyria 62 0.109
379
INT079 Intrahepatic Cholangiocarcinoma 51 0.109
380
DYS015 Dysentery 52 0.109
381
P CNR004 Cone-Rod Dystrophy 2 73 0.109
382
ADR007 Adrenoleukodystrophy 75 0.109
383
P RTN016 Retinal Degeneration 53 0.109
384
CVD001 Covid-19 44 0.108
385
IGR001 Ige Responsiveness, Atopic 59 0.108
386
DBT010 Diabetic Neuropathy 54 0.108
387
NRT001 Neurotic Disorder 53 0.108
388
PPT001 Peptic Esophagitis 52 0.108
389
VTM002 Vitamin B12 Deficiency 48 0.107
390
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.107
391
P TMP001 Temporal Lobe Epilepsy 50 0.107
392
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.107
393
P ANP001 Anaplastic Large Cell Lymphoma 58 0.107
394
c LKM005 Leukemia, T-Cell, Chronic 34 0.107
395
CHR178 Chromosomal Triplication 35 0.107
396
P PLY011 Polycystic Ovary Syndrome 56 0.106
397
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.106
398
MDD018 Middle East Respiratory Syndrome 43 0.106
399
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.106
400
CHL004 Cholelithiasis 49 0.105
401
SPL018 Splenomegaly 48 0.105
402
INT007 Intermediate Coronary Syndrome 55 0.105
403
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.105
404
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.105
405
KRT002 Keratomalacia 47 0.104
406
P MYC084 Mycobacterium Tuberculosis 1 68 0.104
407
c INH020 Inherited Metabolic Disorder 47 0.104
408
ALL006 Allergic Asthma 56 0.104
409
ENT011 Enterocolitis 51 0.104
410
CNT047 Contact Dermatitis 58 0.104
411
ORL015 Oral Squamous Cell Carcinoma 43 0.104
412
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.104
413
URT049 Urate Oxidase, Pseudogene 25 0.104
414
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.103
415
P BRS044 Breast Adenocarcinoma 59 0.103
416
c DLT002 Dilated Cardiomyopathy 79 0.103
417
ARG004 Argyria 27 0.103
418
P LCT001 Lactic Acidosis 51 0.103
419
LPT014 Leptin Deficiency or Dysfunction 74 0.103
420
DYS073 Dysphagia 50 0.103
421
AVN001 Avian Influenza 59 0.102
422
PLY150 Polykaryocytosis Inducer 31 0.102
423
P URT039 Urticaria 58 0.102
424
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.102
425
P CND004 Candidiasis 58 0.102
426
TRN018 Transitional Cell Carcinoma 56 0.101
427
PRP027 Peripheral Vascular Disease 71 0.101
428
ENT004 Enthesopathy 49 0.101
429
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.101
430
P BNG032 Benign Mesothelioma 46 0.101
431
PRT013 Portal Hypertension 59 0.100
432
OST017 Osteomyelitis 64 0.100
433
P AMY004 Amyloidosis 70 0.100
434
VRC005 Varicose Veins 60 0.100
435
P MLN007 Male Infertility 55 0.100
436
ACN002 Acanthosis Nigricans 60 0.100
437
KPS004 Kaposi Sarcoma 75 0.099
438
P MPL001 Maple Syrup Urine Disease 69 0.099
439
BCK006 Back Pain 42 0.099
440
ADR022 Adrenomyeloneuropathy 38 0.099
441
THR013 Thoracic Outlet Syndrome 54 0.099
442
URL001 Urolithiasis 45 0.099
443
P HYP265 Hypotonia 43 0.099
444
IRR002 Irritable Bowel Syndrome 65 0.099
445
P ART023 Arthropathy 62 0.099
446
TRT001 Teratocarcinoma 45 0.098
447
P HMP007 Hemophilia 51 0.098
448
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.098
449
P SRC025 Sarcoidosis 1 70 0.098
450
HMS001 Hemosiderosis 54 0.098
451
P DNG005 Dengue Virus 59 0.098
452
P DYS154 Dystonia 65 0.097
453
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.097
454
P SCL009 Sclerosing Cholangitis 48 0.097
455
c BRN108 Branchiootic Syndrome 1 62 0.097
456
PTT037 Pituitary Tumors 44 0.097
457
NWC001 Newcastle Disease 45 0.096
458
PSY004 Psychotic Disorder 67 0.096
459
P INT099 Intrahepatic Cholestasis of Pregnancy 51 0.096
460
P GRF003 Graft-Versus-Host Disease 72 0.096
461
P RRH023 Rare Hereditary Hemochromatosis 41 0.096
462
AMN003 Amnestic Disorder 54 0.096
463
GST040 Gastric Adenocarcinoma 70 0.096
464
c ACT134 Acute Liver Failure 56 0.096
466
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.096
467
P ANR048 Aniridia 1 63 0.096
468
CHG001 Chagas Disease 66 0.096
469
DSS008 Disease of Mental Health 58 0.095
470
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.095
471
P SYS005 Systemic Scleroderma 68 0.095
472
FBR047 Fibromyalgia 58 0.095
473
CRB037 Cerebral Palsy 69 0.095
474
BRN004 Brain Edema 56 0.095
475
P OPN001 Open-Angle Glaucoma 49 0.095
476
OVR094 Ovarian Epithelial Cancer 38 0.095
477
INS001 Insulinoma 60 0.095
478
P PYL005 Pyelonephritis 56 0.094
479
c PRS136 Prostate Cancer, Hereditary, 6 33 0.094
480
c PRS130 Prostate Cancer, Hereditary, 8 32 0.094
481
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.094
482
c SCL052 Scleroderma, Familial Progressive 61 0.094
483
P GLM040 Glioma Susceptibility 1 81 0.094
484
c CHL119 Cholangitis, Primary Sclerosing 57 0.093
485
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.093
486
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.093
487
CRV045 Cervical Intraepithelial Neoplasia 39 0.093
488
CRH005 Crohn's Colitis 53 0.092
489
P SLP006 Sleep Apnea 69 0.092
490
TRN015 Transient Cerebral Ischemia 63 0.092
491
P MDL005 Medulloblastoma 77 0.092
492
SFT003 Soft Tissue Sarcoma 56 0.092
493
P PLY014 Polycystic Kidney Disease 62 0.092
494
P MCR010 Microcephaly 59 0.092
495
c ALP101 Alpha-Thalassemia 62 0.091
496
ATX010 Ataxia Neuropathy Spectrum 34 0.091
497
ACT064 Acute Necrotizing Encephalitis 33 0.091
498
BLD137 Blood Group--Ahonen 16 0.091
499
P FML011 Familial Adenomatous Polyposis 72 0.091
500
P HYP061 Hypertrophic Cardiomyopathy 70 0.091
501
BLR008 Bilirubin Metabolic Disorder 57 0.091
502
P PRS038 Personality Disorder 65 0.091
503
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.090
504
P THY032 Thyroiditis 52 0.090
505
LNG031 Lung Benign Neoplasm 51 0.090
506
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.090
507
CLR108 Colorectal Adenoma 64 0.090
508
HDN002 Head Injury 46 0.090
509
KRT019 Keratitis, Hereditary 65 0.090
510
RTN017 Retinal Detachment 61 0.089
511
RHM001 Rheumatic Fever 60 0.089
512
CHR074 Choriocarcinoma 47 0.088
513
P HMC002 Homocystinuria 53 0.088
514
c EXD008 Exudative Vitreoretinopathy 1 71 0.088
515
PHR003 Pharyngitis 57 0.088
516
SPN051 Spondylitis 51 0.088
517
PST092 Posttransplant Acute Limbic Encephalitis 29 0.088
518
RSC001 Rosacea 54 0.088
519
HRP004 Herpes Zoster 60 0.088
520
INF009 Inflammatory Spondylopathy 31 0.088
521
MTH071 Methane Production 26 0.087
522
IDP070 Idiopathic Scoliosis 42 0.087
523
GTR002 Goiter 53 0.087
524
GST050 Gastrointestinal System Disease 56 0.087
525
PLS009 Plasma Cell Neoplasm 51 0.087
526
P CNJ013 Conjunctivitis 65 0.087
527
P GCH001 Gaucher's Disease 63 0.087
528
P RTN018 Retinal Disease 53 0.086
529
VLV047 Volvulus of Midgut 49 0.086
530
CNN005 Connective Tissue Disease 68 0.086
531
c FML035 Familial Hyperlipidemia 55 0.086
532
P HYD006 Hydrocephalus 66 0.085
533
P MYC008 Myocarditis 59 0.085
534
P RBL001 Rubella 59 0.085
535
CLF001 Cleft Lip 53 0.085
536
P ADL010 Adult Respiratory Distress Syndrome 65 0.085
537
SBC016 Subacute Delirium 44 0.085
538
c MNN043 Meningioma, Familial 74 0.085
539
AND002 Androgen Insensitivity Syndrome 66 0.085
540
BRN028 Brain Cancer 74 0.085
541
ART016 Aortic Aneurysm 69 0.085
542
P SYP003 Syphilis 58 0.084
543
c MCR129 Microvascular Complications of Diabetes 1 66 0.084
544
MNN042 Meningioma, Radiation-Induced 62 0.084
545
c INF071 Inflammatory Bowel Disease 1 67 0.084
546
P RHB003 Rhabdomyosarcoma 63 0.084
547
c VSC019 Vesicoureteral Reflux 1 57 0.084
548
WST005 West Nile Virus 54 0.084
549
HRT011 Heart Septal Defect 50 0.084
550
ANT024 Anthrax Disease 58 0.084
551
DFF005 Diffuse Large B-Cell Lymphoma 55 0.084
552
PLS011 Plasmacytoma 56 0.084
553
c DRR009 Diarrhea 6 46 0.084
554
GNG013 Gingivitis 59 0.084
555
P NRV007 Nervous System Disease 66 0.084
556
SPN021 Spinal Meningioma 50 0.083
557
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.083
558
TRY001 Trypanosomiasis 50 0.083
559
PRN019 Perinatal Necrotizing Enterocolitis 59 0.083
560
c WLM018 Wilms Tumor 5 61 0.083
561
c ATM099 Autoimmune Uveitis 45 0.083
562
PLG002 Plague 63 0.083
563
P EPD016 Epidermolysis Bullosa 53 0.083
564
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.083
565
SCR001 Secretory Meningioma 41 0.082
566
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.082
567
RNL077 Renal Fibrosis 47 0.082
568
P GRV001 Graves' Disease 55 0.082
569
MSC157 Muscular Dystrophy, Duchenne Type 72 0.082
570
PNC129 Pancreatic Adenocarcinoma 68 0.082
571
SYN007 Synovitis 54 0.082
572
PLC002 Plica Syndrome 36 0.082
573
LMY002 Leiomyoma 52 0.082
574
FDL002 Food Allergy 51 0.082
575
ALL010 Allergic Contact Dermatitis 56 0.082
576
MMM001 Mammary Paget's Disease 53 0.082
577
LYS012 Lysosomal Acid Lipase Deficiency 65 0.081
578
P HMN010 Hemangioma 61 0.081
579
P ANG001 Angelman Syndrome 69 0.081
580
c ATM011 Autoimmune Hepatitis 63 0.081
581
HYD002 Hydronephrosis 60 0.081
582
P LRY044 Larynx Cancer 55 0.081
583
KRT013 Keratolytic Winter Erythema 46 0.081
584
CLR109 Colorectal Adenocarcinoma 51 0.081
585
c SCN007 Secondary Hyperparathyroidism 51 0.081
586
KHL003 Kohlschutter-Tonz Syndrome 65 0.080
587
RBS001 Rabies 58 0.080
588
P MYS005 Myositis 56 0.080
589
CYT008 Cytomegalovirus Infection 57 0.080
590
VRL011 Viral Infectious Disease 61 0.080
591
c CHR064 Chronic Monocytic Leukemia 33 0.080
592
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.079
593
IRN001 Iron Deficiency Anemia 59 0.079
594
P SBS003 Substance Abuse 55 0.079
595
P INT143 Interstitial Cystitis 61 0.079
596
P MVM001 Movement Disease 63 0.079
597
VSC002 Vascular Dementia 57 0.079
598
HND015 Hand Skill, Relative 33 0.079
599
SLP001 Sleeping Sickness 54 0.079
600
WLL004 Wallerian Degeneration 39 0.079
601
P INT068 Intestinal Disease 53 0.079
602
c GLC092 Glaucoma, Primary Open Angle 62 0.079
603
CHL067 Cholecystitis 57 0.078
604
OST115 Osteonecrosis of the Jaw 40 0.078
605
P OBS001 Obstructive Jaundice 50 0.078
606
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.078
607
P ZLL001 Zellweger Syndrome 57 0.078
608
INF034 Infective Endocarditis 53 0.078
609
PRP016 Paraplegia 52 0.078
610
MNN009 Meningoencephalitis 49 0.078
611
PNC001 Pancytopenia 54 0.078
612
P CLC063 Celiac Disease 1 66 0.078
613
HYP081 Hypolipoproteinemia 51 0.078
614
PST053 Postherpetic Neuralgia 40 0.078
615
P AXN002 Axenfeld-Rieger Syndrome 59 0.078
616
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.078
617
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.078
618
CRN030 Coronary Stenosis 50 0.077
619
YLL002 Yellow Fever 61 0.077
620
P HRS035 Hirschsprung Disease 1 65 0.077
621
P MYP006 Myopia 55 0.077
622
INT066 Interstitial Lung Disease 60 0.077
623
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.077
624
P ADL017 Adult T-Cell Leukemia 56 0.077
625
ZLL002 Zollinger-Ellison Syndrome 55 0.076
626
HPT022 Hepatoblastoma 56 0.076
627
MSC007 Muscle Hypertrophy 64 0.076
628
P VNT002 Ventricular Septal Defect 60 0.076
629
PLS007 Plasmodium Falciparum Malaria 52 0.076
630
ADP007 Adie Pupil 39 0.076
631
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.076
632
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.076
633
P FLL037 Follicular Lymphoma 67 0.076
634
P SPN046 Spinal Muscular Atrophy 62 0.076
635
P PLY018 Polycythemia 56 0.075
636
SKN019 Skin Melanoma 68 0.075
637
TBC004 Tobacco Addiction 64 0.075
638
SPT004 Septic Arthritis 58 0.075
639
XNT003 Xanthomatosis 49 0.075
640
P ANT006 Antiphospholipid Syndrome 55 0.075
641
MGL001 Megaloblastic Anemia 51 0.075
642
AMN001 Amenorrhea 54 0.075
643
P SCL057 Scoliosis, Isolated 1 41 0.075
644
BLR001 Biliary Atresia 50 0.075
645
LYM027 Lymphopenia 58 0.075
646
P PTT006 Pituitary Adenoma 55 0.075
647
P PNC025 Panic Disorder 53 0.075
648
LWC001 Low Compliance Bladder 43 0.075
649
GRN017 Granulocytopenia 44 0.075
650
c BCT007 Bacterial Meningitis 55 0.074
651
P MNC007 Monocytic Leukemia 53 0.074
652
P SLP005 Sleep Disorder 59 0.074
653
c GCH015 Gaucher Disease, Type I 70 0.074
654
P TBR001 Tuberous Sclerosis 70 0.074
655
KRT006 Keratoconjunctivitis 53 0.074
656
P ALP009 Alopecia Areata 60 0.074
657
HPT082 Hepatic Adenomas, Familial 44 0.074
658
HNM002 Hinman Syndrome 27 0.074
659
PLC008 Placenta Disease 50 0.074
660
ALR002 Al-Raqad Syndrome 33 0.074
661
SPS057 Spasticity 45 0.074
662
P MYS003 Myasthenia Gravis 68 0.073
663
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.073
664
P OPT006 Optic Nerve Disease 60 0.073
665
P PTS002 Ptosis 53 0.073
666
HYP080 Hypogonadism 50 0.073
667
CHR073 Choreatic Disease 52 0.073
668
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.073
669
APP008 Appendicitis 61 0.073
670
P APL001 Aplastic Anemia 74 0.073
671
IGG001 Iga Glomerulonephritis 48 0.073
672
c PRM005 Primary Hyperparathyroidism 58 0.073
673
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.073
674
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.073
675
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.073
676
P TXP001 Toxoplasmosis 60 0.073
677
PRP080 Peripheral Artery Disease 53 0.073
678
CYS013 Cystinuria 63 0.072
679
JPN002 Japanese Encephalitis 57 0.072
680
PTH003 Pathologic Nystagmus 52 0.072
681
TNS005 Tonsillitis 57 0.072
682
TBR011 Tuberculous Meningitis 48 0.072
683
P TRT010 Teratoma 52 0.072
684
ETN001 Eating Disorder 60 0.072
685
P MYC033 Myoclonus 46 0.072
687
BRN056 Bronchopulmonary Dysplasia 57 0.071
688
ILS001 Ileus 51 0.071
689
LKP003 Leukoplakia 39 0.071
690
THR016 Thrombophlebitis 51 0.071
691
P PRN023 Prion Disease 57 0.071
692
P ASP006 Aspergillosis 69 0.071
693
P DRM010 Dermatomyositis 61 0.071
694
HRY003 Hairy Cell Leukemia 55 0.071
695
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.071
696
PST021 Postpartum Depression 50 0.071
697
P SJG008 Sjogren Syndrome 61 0.071
698
PRS047 Prostatitis 56 0.071
699
PRT011 Protein C Deficiency 44 0.071
700
P MMP001 Mumps 58 0.071
701
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.071
702
c FML021 Familial Hypercholesterolemia 66 0.070
703
P MJR007 Major Affective Disorder 1 43 0.070
704
P NRF002 Neurofibromatosis 56 0.070
705
49X006 49, Xxxxy Syndrome 41 0.070
706
MST004 Mast Cell Neoplasm 42 0.070
707
EXT007 Extracutaneous Mastocytoma 38 0.070
708
URT010 Ureteral Obstruction 45 0.070
709
P ATR005 Atrophic Gastritis 50 0.070
710
P FRG001 Fragile X Syndrome 70 0.070
711
ACR007 Acromegaly 71 0.070
712
CND006 Candida Glabrata 32 0.070
713
LYS002 Lysosomal Storage Disease 52 0.070
714
P SNS001 Sensorineural Hearing Loss 60 0.069
715
P ALP106 Alport Syndrome 1, X-Linked 55 0.069
716
P THY023 Thymoma 65 0.069
717
c THY107 Thymoma, Familial 52 0.069
718
c FML001 Familial Atrial Fibrillation 65 0.069
719
P MLG074 Malignant Mesenchymoma 40 0.069
720
BRC012 Brucellosis 64 0.069
721
INT075 Intracranial Hypertension 53 0.069
722
CTN007 Cutaneous Leishmaniasis 62 0.069
723
INT017 Intestinal Schistosomiasis 48 0.069
724
c PRD040 Periodontitis, Chronic 53 0.069
725
GLS001 Gliosarcoma 54 0.069
726
DRY001 Dry Eye Syndrome 47 0.069
727
ING001 Inguinal Hernia 60 0.069
728
OBS002 Obsessive-Compulsive Disorder 68 0.069
729
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.068
730
c GRV008 Graves Disease 1 56 0.068
731
PRN011 Pernicious Anemia 53 0.068
732
DWR001 Dwarfism 44 0.068
733
BRN002 Bronchiolitis 59 0.068
734
P MTR014 Motor Neuron Disease 65 0.068
735
NCL008 Nuclear Ribonucleic Acid 16 0.068
736
P ICH004 Ichthyosis 54 0.068
737
BWN006 Bowen's Disease 32 0.068
738
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.068
739
DMY004 Demyelinating Disease 52 0.068
740
c HPT015 Hepatitis D 49 0.068
741
P CTN015 Cutaneous T Cell Lymphoma 49 0.067
742
c HYP272 Hypercholesterolemia, Familial, 3 44 0.067
743
SXL003 Sexual Disorder 47 0.067
744
THY030 Thyroid Gland Disease 52 0.067
745
RFS006 Refsum Disease, Classic 64 0.067
746
P GLL018 Gallbladder Cancer 57 0.067
747
P CHN012 Chondrosarcoma 56 0.067
748
RYS001 Reye Syndrome 51 0.067
749
c SVR005 Severe Pre-Eclampsia 50 0.067
750
PSR001 Psoriatic Arthritis 61 0.067
751
CLL003 Cellulitis 54 0.067
752
PNM008 Pneumothorax 56 0.067
753
MCR013 Microphthalmia 57 0.066
754
c PSR023 Psoriasis 1 52 0.066
755
BLL006 Bullous Pemphigoid 62 0.066
756
c OVR114 Ovarian Cancer 1 38 0.066
757
NRT004 Neuritis 52 0.066
758
P HYP040 Hypospadias 51 0.066
759
GLS018 Glass Syndrome 57 0.066
760
c HMP029 Hemophilia a 67 0.066
761
NWB001 Newborn Respiratory Distress Syndrome 58 0.066
762
ACT084 Acute Stress Disorder 47 0.066
763
CHR100 Chronic Ulcer of Skin 55 0.066
764
P CRN037 Craniosynostosis 68 0.065
765
CLR030 Clear Cell Renal Cell Carcinoma 53 0.065
766
SPP011 Suppression of Tumorigenicity 12 59 0.065
767
CMM005 Common Cold 57 0.065
768
P INT070 Intestinal Obstruction 58 0.065
769
c HMC039 Hemochromatosis, Type 1 74 0.065
770
LYM040 Lymphoblastic Lymphoma 54 0.065
771
SHG001 Shigellosis 60 0.065
772
RYN005 Raynaud Phenomenon 47 0.065
773
SDD001 Sudden Infant Death Syndrome 61 0.065
774
ESP002 Esophageal Varix 51 0.065
775
P STR020 Strabismus 55 0.065
776
AZS001 Azoospermia 50 0.065
777
MYF002 Myofascial Pain Syndrome 42 0.064
778
STN013 Stenotrophomonas Maltophilia Infection 25 0.064
779
IMM165 Immunoglobulin Switch Sequences 15 0.064
780
P DBT005 Diabetes Insipidus 55 0.064
781
MCH006 Mechanical Strabismus 42 0.064
782
LNT004 Lentigines 50 0.064
783
SCB001 Scabies 50 0.064
784
PST028 Post-Traumatic Stress Disorder 58 0.064
785
P SML001 Small Cell Carcinoma 52 0.064
786
SCR011 Scrapie 39 0.064
787
TCK001 Tick-Borne Encephalitis 56 0.064
788
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.064
789
GRD007 Grade Iii Astrocytoma 59 0.064
790
HRN026 Hernia, Hiatus 47 0.064
791
WTH001 Withdrawal Disorder 48 0.064
792
MCL006 Macular Retinal Edema 55 0.063
793
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.063
794
CRT015 Carotid Artery Occlusion 45 0.063
795
IMP004 Impetigo 49 0.063
796
NRN004 Neuroendocrine Tumor 55 0.063
797
P MTC069 Mitochondrial Disorders 56 0.063
798
FCT007 Factor Vii Deficiency 67 0.063
799
MLK006 Milk Allergy 48 0.063
800
c MCR112 Microvascular Complications of Diabetes 2 41 0.063
801
THR004 Thrombocytosis 51 0.063
802
KRT001 Keratoconjunctivitis Sicca 49 0.063
803
FCL014 Focal Epilepsy 54 0.063
804
FLR002 Filariasis 55 0.063
805
SLC006 Silicosis 56 0.063
806
ART001 Arterial Tortuosity Syndrome 66 0.062
807
INC002 Inclusion Body Myositis 58 0.062
808
CRC021 Carcinosarcoma 62 0.062
809
ART002 Arts Syndrome 64 0.062
810
BCT002 Bacterial Vaginosis 53 0.062
811
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.062
812
CHL056 Cheilitis 48 0.062
813
RHM028 Rheumatic Heart Disease 53 0.062
814
INT002 Intermittent Claudication 61 0.062
815
c PSR017 Psoriasis 2 53 0.062
816
c PSR032 Psoriasis 11 47 0.062
817
c PSR028 Psoriasis 7 42 0.062
818
c PSR018 Psoriasis 13 41 0.062
819
STF001 Stiff-Person Syndrome 60 0.062
820
LST001 Listeriosis 56 0.062
821
THY111 Thyroid Carcinoma, Familial Medullary 67 0.062
822
c ACT135 Acute Graft Versus Host Disease 52 0.062
823
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.061
824
c BCT013 Bacterial Pneumonia 48 0.061
825
c CHR682 Chronic Bilirubin Encephalopathy 39 0.061
826
c MJR006 Major Affective Disorder 5 33 0.061
827
VSC003 Visceral Leishmaniasis 55 0.061
828
HMT002 Hematologic Cancer 62 0.061
829
FSC004 Fasciitis 50 0.061
830
CYN002 Cyanosis, Transient Neonatal 45 0.061
831
BCT004 Bacteriuria 49 0.061
832
MYC088 Mycobacterium Avium Complex Infections 29 0.061
833
LYM009 Lymphocytic Choriomeningitis 47 0.061
834
P AVS003 Avascular Necrosis 42 0.061
835
LMB062 Limb Ischemia 55 0.061
836
VRC001 Varicocele 49 0.061
837
HYP017 Hypophosphatemia 50 0.061
838
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.061
839
PYR009 Pyridoxine Deficiency Anemia 34 0.061
840
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.061
841
c MST023 Mesothelioma, Malignant 57 0.061
842
MNT001 Mantle Cell Lymphoma 69 0.061
843
BRT054 Brittle Bone Disorder 72 0.061
844
c JVN010 Juvenile Rheumatoid Arthritis 64 0.060
845
PLR007 Pleural Empyema 50 0.060
846
APH002 Aphasia 57 0.060
847
P PLM034 Pulmonary Emphysema 55 0.060
848
c FNC027 Fanconi Anemia, Complementation Group a 81 0.060
849
SYN036 Syncope 45 0.060
850
ONC002 Onchocerciasis 52 0.060
851
SCH012 Schizoaffective Disorder 50 0.060
852
P SHR001 Short Bowel Syndrome 53 0.060
853
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.060
854
P LCH002 Lichen Planus 53 0.060
855
PLC007 Placental Abruption 48 0.060
856
TRD006 Tardive Dyskinesia 54 0.060
857
PLR008 Pleurisy 50 0.060
858
CRD223 Cardiac Arrhythmia 60 0.060
859
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.060
860
PLL012 Pollen Allergy 46 0.060
861
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.060
862
c MLG084 Malignant Fibrous Histiocytoma 63 0.059
863
P BRN022 Bronchiectasis 59 0.059
864
VTM033 Vitamin K Deficiency Bleeding 48 0.059
865
PLY001 Polycythemia Vera 69 0.059
866
KRN002 Kearns-Sayre Syndrome 63 0.059
867
c HMP004 Hemophilia B 68 0.059
868
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.059
869
LYM017 Lyme Disease 64 0.059
870
RFR010 Refractory Anemia 48 0.059
871
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.059
872
RDN001 Reading Disorder 40 0.059
873
P NGH001 Night Blindness 48 0.059
874
P BNG030 Benign Ependymoma 60 0.059
875
CMP010 Complex Regional Pain Syndrome 58 0.059
876
P PRP034 Purpura Fulminans 43 0.059
877
OCL006 Ocular Hypertension 53 0.059
878
THY122 Thyroid Gland Cancer 57 0.059
879
KWS001 Kwashiorkor 44 0.059
880
P TTR001 Tetralogy of Fallot 70 0.059
881
AND005 Androgen Insensitivity Syndrome, Mild 19 0.059
882
WRN001 Werner Syndrome 69 0.059
883
ANG005 Anogenital Venereal Wart 55 0.059
884
CRP001 Carpal Tunnel Syndrome 67 0.059
885
P PMP001 Pemphigus 54 0.059
886
ADG002 Audiogenic Seizures 25 0.059
887
MCR004 Macroglobulinemia 49 0.058
888
CRD137 Cardiogenic Shock 47 0.058
889
P MYT002 Myotonic Dystrophy 49 0.058
890
CLL010 Cellular Ependymoma 54 0.058
891
c MJR003 Major Affective Disorder 6 33 0.058
892
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.058
893
TST014 Testicular Cancer 46 0.058
894
KWS002 Kawasaki Disease 65 0.058
895
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.058
896
MYM001 Myoma 54 0.058
897
P VTR007 Vitreoretinopathy 46 0.058
898
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.058
899
c DNG003 Dengue Disease 59 0.058
900
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.058
901
HYP025 Hyperphosphatemia 48 0.058
902
c INF145 Infantile Liver Failure Syndrome 1 50 0.058
903
HRT012 Heart Valve Disease 53 0.058
904
ALC006 Alcoholic Hepatitis 61 0.058
905
P LMY004 Leiomyosarcoma 63 0.058
906
P OLG002 Oligodendroglioma 67 0.058
907
BRS099 Breast Ductal Carcinoma 62 0.057
908
P HML001 Hemolytic-Uremic Syndrome 53 0.057
909
KLD004 Keloid Disorder 40 0.057
910
P RTT002 Rett Syndrome 80 0.057
911
P FRD001 Friedreich Ataxia 64 0.057
912
NRM005 Neuromuscular Disease 64 0.057
913
CRT013 Carotid Stenosis 50 0.057
914
NTR046 Neutrophil Migration 50 0.057
915
BLR002 Bile Reflux 39 0.057
916
PRP083 Porphyria, Acute Intermittent 64 0.057
917
RTN020 Retinal Vascular Disease 46 0.057
918
P CHR285 Chronic Myelomonocytic Leukemia 60 0.057
919
ALC009 Alcoholic Liver Cirrhosis 53 0.057
920
THY125 Thyroid Gland Medullary Carcinoma 50 0.057
921
MYL031 Myeloproliferative Neoplasm 66 0.057
922
c WLM013 Wilms Tumor 1 65 0.057
923
P VSC018 Visceral Steatosis 33 0.057
924
ADR016 Adrenal Cortical Carcinoma 48 0.057
925
P BNC003 Bone Cancer 58 0.057
926
P LKD001 Leukodystrophy 59 0.056
927
CLF004 Cleft Lip/palate 54 0.056
928
RFR003 Refractive Error 43 0.056
929
DCT002 Ductal Carcinoma in Situ 59 0.056
930
MYL005 Myelofibrosis 70 0.056
931
HMP005 Hemiplegia 55 0.056
932
ACT003 Acute Kidney Tubular Necrosis 45 0.056
933
SCH003 Schizophreniform Disorder 56 0.056
934
ATN004 Autonomic Neuropathy 45 0.056
935
EXN003 Exencephaly 31 0.056
936
AYM001 Ayme-Gripp Syndrome 57 0.056
937
DBT002 Diabetic Autonomic Neuropathy 41 0.056
938
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.056
939
PRC013 Pericarditis 54 0.056
940
IRD001 Iridocyclitis 53 0.056
941
P END047 Endophthalmitis 53 0.056
942
P GLL022 Guillain-Barre Syndrome 59 0.056
943
PRM003 Premature Ejaculation 44 0.056
944
PLY100 Polyploidy 40 0.056
945
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.056
946
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.056
947
GNG003 Gingival Recession 44 0.055
948
c MJR008 Major Affective Disorder 2 35 0.055
949
c MJR023 Major Affective Disorder 7 33 0.055
950
c MJR004 Major Affective Disorder 4 28 0.055
951
CHR066 Chronic Fatigue Syndrome 61 0.055
952
P FRN006 Frontotemporal Dementia 68 0.055
953
P ANG015 Angioedema 57 0.055
954
LPR001 Lepromatous Leprosy 50 0.055
955
P VNW001 Von Willebrand's Disease 65 0.055
956
ATR057 Atrioventricular Block 55 0.055
957
HST010 Histiocytosis 48 0.055
958
PFF001 Pfeiffer Syndrome 79 0.055
959
AST006 Astigmatism 47 0.055
960
P AGM001 Agammaglobulinemia 65 0.055
961
BLD131 Bladder Urothelial Carcinoma 62 0.055
962
P EHL001 Ehlers-Danlos Syndrome 58 0.055
963
c HNT004 Huntington Disease-Like 2 50 0.055
964
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.055
965
SCH036 Scheie Syndrome 72 0.055
966
DMP001 Dumping Syndrome 44 0.055
967
ILT001 Ileitis 50 0.055
968
TTH006 Tooth Disease 46 0.055
969
AMB002 Amblyopia 49 0.055
970
SPP007 Suppression Amblyopia 39 0.055
971
PRT018 Portal Vein Thrombosis 50 0.054
972
BLC012 Bile Acid Malabsorption, Primary 45 0.054
973
END041 Endometrial Adenocarcinoma 63 0.054
974
c TBR025 Tuberous Sclerosis 1 77 0.054
975
P HRD011 Hereditary Spherocytosis 60 0.054
976
ATM052 Autoimmune Disease 1 37 0.054
977
CYS005 Cysticercosis 53 0.054
978
P CLL015 Collagen Disease 47 0.054
979
P MTH007 Methemoglobinemia 46 0.054
980
HLL004 Hellp Syndrome 54 0.054
981
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.054
982
GLB001 Gilbert Syndrome 58 0.054
983
c DPH024 Diaphragmatic Hernia, Congenital 63 0.054
984
P RTN022 Retinal Vein Occlusion 53 0.054
985
ADR004 Adrenal Cortical Adenocarcinoma 39 0.054
986
AVD001 Avoidant Personality Disorder 51 0.054
987
c HMG029 Hemoglobin Se Disease 39 0.054
988
c ART101 Aortic Valve Disease 2 65 0.054
989
LSC001 Lesch-Nyhan Syndrome 62 0.054
990
c GZP005 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 44 0.054
991
HYP043 Hyperandrogenism 48 0.054
992
PRM329 Premature Aging 35 0.054
993
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.054
994
ATN005 Autonomic Dysfunction 46 0.054
995
P MMB011 Membranous Nephropathy 50 0.054
996
INT067 Interstitial Nephritis 48 0.053
997
LRN003 Learning Disability 49 0.053
998
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.053
999
BNN003 Bone Inflammation Disease 48 0.053
1000
NRL005 Neurilemmoma 60 0.053
1001
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.053
1002
P OPT009 Optic Neuritis 57 0.053
1003
APN008 Apnea, Obstructive Sleep 64 0.053
1004
DRM011 Dermatophytosis 52 0.053
1005
OST011 Osteomalacia 52 0.053
1006
ASP007 Aspiration Pneumonia 48 0.053
1007
PPL049 Papillon-Lefevre Syndrome 65 0.053
1008
c BLR024 Biliary Cirrhosis, Primary, 1 30 0.053
1009
P ART005 Arteriovenous Malformation 65 0.053
1010
CHL013 Cholecystolithiasis 37 0.053
1011
FNG017 Fungal Infectious Disease 53 0.053
1012
SNL007 Senile Cataract 42 0.052
1013
CRC006 Carcinoid Syndrome 55 0.052
1014
DCB001 Decubitus Ulcer 61 0.052
1015
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 0.052
1016
WST001 West Syndrome 61 0.052
1017
ECH003 Echinococcosis 53 0.052
1018
NRF007 Neurofibroma 64 0.052
1019
P FNC004 Fanconi Syndrome 50 0.052
1020
P FTL001 Fetal Alcohol Syndrome 57 0.052
1021
DGN001 Degenerative Disc Disease 48 0.052
1022
P CHR071 Charcot-Marie-Tooth Disease 65 0.052
1023
MYF001 Myofibroma 45 0.052
1024
c ACR116 Aicardi-Goutieres Syndrome 1 52 0.052
1025
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.052
1026
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.052
1027
P PLY006 Polydactyly 59 0.052
1028
ASP003 Aseptic Meningitis 51 0.052
1029
PYL006 Pyloric Stenosis 48 0.052
1030
c PRG020 Paragangliomas 3 39 0.051
1031
NCR007 Necrotizing Fasciitis 48 0.051
1032
P HMN032 Human Herpesvirus 8 47 0.051
1033
ANP008 Anaplastic Oligoastrocytoma 30 0.051
1034
ANR004 Anuria 46 0.051
1035
CHK001 Chikungunya 57 0.051
1036
P HMR003 Hemorrhagic Disease 53 0.051
1037
VGN023 Vaginitis 54 0.051
1038
PPL001 Papillary Adenoma 44 0.051
1039
MCR011 Microinvasive Gastric Cancer 43 0.051
1040
LPT001 Leptospirosis 66 0.051
1041
GST037 Gastroparesis 54 0.051
1042
P PSD015 Pseudohypoparathyroidism 56 0.051
1043
P FNC034 Fanconi Renotubular Syndrome 2 40 0.051
1044
P PLY041 Polymyositis 57 0.051
1045
SPN027 Spinal Stenosis 59 0.051
1046
RTC005 Reticulosarcoma 47 0.051
1047
P NRC002 Narcolepsy 52 0.051
1048
CCC001 Coccidioidomycosis 58 0.051
1049
CYT018 Cytochrome P450 2d6 Variant 27 0.051
1050
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.051
1051
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.051
1052
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.051
1053
PRS063 Paresthesia