Search results for Norepinephrine

1713 hits were found for Norepinephrine

# Family MCID Name MIFTS Score
1
c ORT011 Orthostatic Hypotension 1 43 21.423
2
DPM001 Dopamine Beta-Hydroxylase Deficiency 54 20.927
3
PST048 Postural Orthostatic Tachycardia Syndrome 46 16.480
4
TXC005 Toxic Shock Syndrome 61 15.590
5
P ORT004 Orthostatic Intolerance 61 13.877
6
c HYP595 Hypertension, Essential 84 10.708
7
P PHC003 Pheochromocytoma 70 10.259
8
MNT002 Mental Depression 56 9.316
9
P MJR001 Major Depressive Disorder 68 8.808
10
DPR016 Depression 64 8.806
11
PRT058 Pure Autonomic Failure 58 8.200
12
P ATT013 Attention Deficit-Hyperactivity Disorder 65 7.882
13
ADR040 Adrenal Gland Pheochromocytoma 45 7.761
14
CRD137 Cardiogenic Shock 56 5.625
15
c ACT071 Acute Kidney Failure 60 5.616
16
PRT037 Pertussis 49 5.457
17
HYP056 Hypoglycemia 65 5.241
18
PST028 Post-Traumatic Stress Disorder 58 4.922
19
END040 Endogenous Depression 54 4.699
20
ISC004 Ischemia 61 4.546
21
ANX010 Anxiety 70 4.446
22
P NRB001 Neuroblastoma 66 4.351
23
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 4.299
24
c ATR087 Atrial Standstill 1 74 4.215
25
P PNC025 Panic Disorder 52 4.078
26
P BPL003 Bipolar Disorder 56 3.978
27
P PRK039 Parkinsonism 55 3.938
28
c PRC016 Pre-Eclampsia 64 3.933
29
PNG002 Pain Agnosia 51 3.912
30
48X005 48,xyyy 39 3.895
31
TRM010 Traumatic Brain Injury 50 3.871
32
MDD011 Mood Disorder 61 3.829
33
GNR004 Generalized Anxiety Disorder 54 3.745
34
c DLT002 Dilated Cardiomyopathy 79 3.716
35
SYN036 Syncope 44 3.666
36
CNG034 Congestive Heart Failure 69 3.661
37
HYP060 Hyperinsulinism 53 3.628
38
HYP266 Hypoxia 56 3.593
39
P SLP006 Sleep Apnea 69 3.571
40
P PRM227 Primary Orthostatic Hypotension 24 3.567
41
c MJR022 Major Affective Disorder 8 37 3.557
42
c MJR024 Major Affective Disorder 9 40 3.557
43
P MYC007 Myocardial Infarction 69 3.538
44
MLT157 Multiple System Atrophy 1 69 3.536
45
ATN005 Autonomic Dysfunction 45 3.446
46
BRN071 Brain Injury 50 3.415
47
P HRT032 Heart Disease 84 3.339
48
HYP066 Hyperglycemia 60 3.322
49
P ECL001 Eclampsia 52 3.306
50
P CRD119 Cardiac Arrest 68 3.283
51
SPN186 Spinal Cord Injury 60 3.249
52
HPT014 Hepatorenal Syndrome 49 3.178
53
PRT013 Portal Hypertension 59 3.172
54
P PLM037 Pulmonary Hypertension 69 3.168
55
P KDN018 Kidney Disease 71 3.158
56
STR067 Stroke, Ischemic 79 3.143
57
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 3.125
58
FBR047 Fibromyalgia 57 3.085
59
P SZR006 Seizure Disorder 69 3.077
60
c ACT075 Acute Myocardial Infarction 55 3.073
61
CYT002 Cytokine Deficiency 43 3.059
62
NRT001 Neurotic Disorder 56 3.052
63
P ADL010 Adult Respiratory Distress Syndrome 70 3.052
64
PLM010 Pulmonary Edema 54 2.969
65
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 2.959
66
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 2.959
67
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 2.959
68
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 2.959
69
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 2.959
70
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 2.959
71
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 2.959
72
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 2.959
73
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 2.959
74
P PRK057 Parkinson Disease, Late-Onset 79 2.938
75
ATN004 Autonomic Neuropathy 42 2.919
76
ALC007 Alcohol Dependence 65 2.898
77
LPP008 Lipoprotein Quantitative Trait Locus 65 2.869
78
P CHR345 Chronic Pain 50 2.838
79
ANT039 Antisynthetase Syndrome 55 2.814
80
OBS002 Obsessive-Compulsive Disorder 67 2.812
81
P HYP086 Hypothyroidism 68 2.789
82
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.743
83
ACT084 Acute Stress Disorder 53 2.739
84
P NRP001 Neuropathy 59 2.739
85
TTN003 Tetanus 64 2.733
86
P TRM003 Tremor 50 2.691
87
CCN002 Cocaine Abuse 49 2.682
88
HYP005 Hypokalemia 55 2.679
89
SXL003 Sexual Disorder 49 2.678
90
P PRG013 Paraganglioma 57 2.662
91
CRB039 Cerebrovascular Disease 65 2.658
92
ANR007 Anorexia Nervosa 59 2.642
93
c MGR028 Migraine with or Without Aura 1 63 2.581
94
c TYP009 Type 2 Diabetes Mellitus 91 2.577
95
PRT036 Peritonitis 65 2.576
96
P HYP076 Hyperthyroidism 53 2.554
97
P ALZ034 Alzheimer Disease 87 2.553
98
P DBT009 Diabetes Mellitus 67 2.522
99
HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 61 2.502
100
CHL014 Cholera 62 2.499
101
ART140 Arteries, Anomalies of 52 2.466
102
LVR012 Liver Cirrhosis 62 2.447
103
P DYS021 Dysautonomia 38 2.401
104
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 2.377
105
P HDC001 Headache 56 2.376
106
AGN016 Aging 53 2.365
107
c ORT012 Orthostatic Hypotension 2 21 2.348
108
P CRN300 Coronary Heart Disease 1 73 2.345
109
P RNV001 Renovascular Hypertension 48 2.341
110
PRS045 Prostatic Hypertrophy 53 2.328
111
CRD132 Cardiac Conduction Defect 59 2.324
112
P NRC002 Narcolepsy 55 2.312
113
CNS004 Constipation 56 2.269
114
ETN001 Eating Disorder 59 2.262
115
P SBS003 Substance Abuse 54 2.257
116
GLL008 Gilles De La Tourette Syndrome 64 2.249
117
IRN002 Iron Metabolism Disease 56 2.248
118
P HPT023 Hepatocellular Carcinoma 95 2.245
119
AMN003 Amnestic Disorder 53 2.238
120
OCL069 Ocular Motor Apraxia 57 2.232
121
P SCH015 Schizophrenia 74 2.225
122
47X002 47,xyy 47 2.201
123
ANX004 Anoxia 40 2.191
124
RST023 Resting Heart Rate, Variation in 40 2.191
125
END086 End Stage Renal Disease 54 2.186
126
P PRS038 Personality Disorder 65 2.179
127
P PRP019 Peripheral Nervous System Disease 57 2.156
128
GLL048 Glial Tumor 51 2.141
129
MTB004 Metabolic Acidosis 48 2.138
130
GLM045 Glioma 62 2.132
131
AND005 Androgen Insensitivity Syndrome, Mild 21 2.103
132
CCN001 Cocaine Dependence 47 2.077
133
ALL029 Allergic Disease 61 2.065
134
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 2.044
135
P SLP005 Sleep Disorder 61 2.027
136
CRB009 Cerebritis 43 2.008
137
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 2.008
138
P ATS364 Autism 72 1.986
139
ANG054 Angina Pectoris 65 1.984
140
BRN004 Brain Edema 54 1.968
141
c TYP008 Type 1 Diabetes Mellitus 77 1.964
142
MLG157 Malignant Pheochromocytoma 37 1.961
143
IMP005 Impotence 52 1.951
144
PSY004 Psychotic Disorder 66 1.949
145
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 1.947
146
c HYP836 Hypercholesterolemia, Familial, 1 73 1.932
147
PRS021 Prostatic Adenoma 43 1.927
148
PRS129 Prostatic Hyperplasia, Benign 48 1.917
149
c ATS007 Autism Spectrum Disorder 71 1.916
150
MLD018 Mild Cognitive Impairment 48 1.915
151
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 1.906
152
P LCT001 Lactic Acidosis 50 1.905
153
P EPL164 Epilepsy 70 1.895
154
WTH001 Withdrawal Disorder 47 1.891
155
URM002 Uremia 47 1.883
156
P BLD124 Bleeding Disorder, Platelet-Type, 11 68 1.882
157
ADG002 Audiogenic Seizures 25 1.876
158
HDN002 Head Injury 44 1.872
159
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 1.857
160
APN008 Apnea, Obstructive Sleep 66 1.854
161
SCL003 Social Phobia 48 1.851
162
P MJR007 Major Affective Disorder 1 42 1.841
163
P FML187 Familial Hypertension 34 1.840
164
P PLY011 Polycystic Ovary Syndrome 57 1.835
165
GLC003 Glucose Intolerance 53 1.831
166
P HPT021 Hepatitis 68 1.819
167
c HPT003 Hepatitis a 63 1.819
168
CRT015 Carotid Artery Occlusion 45 1.818
169
P RNL015 Renal Hypertension 45 1.808
170
P DDN001 Duodenal Ulcer 52 1.788
171
P CRD246 Cardiovascular System Disease 55 1.779
172
HPT004 Hepatic Coma 43 1.769
173
P PTS002 Ptosis 52 1.761
174
P GLM040 Glioma Susceptibility 1 70 1.758
175
P PNC035 Pancreatic Cancer 87 1.745
176
P VSC007 Vascular Disease 62 1.733
177
P PRC031 Preeclampsia/eclampsia 1 43 1.733
178
VRC005 Varicose Veins 59 1.727
179
SRT004 Serotonin Syndrome 54 1.725
180
DYS009 Dysthymic Disorder 51 1.720
181
INT075 Intracranial Hypertension 52 1.713
182
P HYP061 Hypertrophic Cardiomyopathy 68 1.711
183
BRK012 Broken Heart Syndrome 42 1.692
184
IRR002 Irritable Bowel Syndrome 64 1.687
185
HYP030 Hypoactive Sexual Desire Disorder 40 1.680
186
RHB024 Rhabdomyosarcoma 2 65 1.677
187
ADL002 Adult Syndrome 69 1.677
188
PLM129 Pulmonary Disease, Chronic Obstructive 74 1.672
189
P PNC044 Pancreatitis 61 1.672
190
P ENC018 Encephalopathy 62 1.659
191
P ATR011 Atrial Fibrillation 66 1.653
192
P BRS047 Breast Cancer 97 1.650
193
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 1.648
194
P OVR042 Ovarian Cancer 88 1.646
195
c MLT160 Multiple Endocrine Neoplasia, Type Iia 67 1.645
196
RYN005 Raynaud Phenomenon 45 1.644
197
CHG001 Chagas Disease 65 1.639
198
DBT010 Diabetic Neuropathy 54 1.632
199
OPT003 Opiate Dependence 49 1.627
200
P DYS154 Dystonia 64 1.613
201
SBC016 Subacute Delirium 42 1.608
202
P MYC008 Myocarditis 59 1.608
203
HPT019 Hepatic Encephalopathy 59 1.601
204
ORL011 Oral Cancer 60 1.598
205
P INT143 Interstitial Cystitis 59 1.595
206
CHR066 Chronic Fatigue Syndrome 59 1.594
207
MLN003 Melancholia 41 1.580
208
P DMN002 Dementia 65 1.580
209
P MLT020 Multiple Sclerosis 79 1.567
210
P LVR013 Liver Disease 68 1.550
211
ATR057 Atrioventricular Block 54 1.548
212
P RHM011 Rheumatoid Arthritis 81 1.545
213
P ALP008 Alopecia 53 1.532
214
P NJM001 Nijmegen Breakage Syndrome 75 1.527
215
SQM013 Squamous Cell Carcinoma, Head and Neck 75 1.527
216
RDN001 Reading Disorder 40 1.527
217
P ALC033 Alcohol Use Disorder 67 1.525
219
BLM002 Bulimia Nervosa 56 1.500
220
P CLR023 Colorectal Cancer 100 1.481
221
CRN019 Coronary Artery Vasospasm 47 1.469
222
P STR092 Striatal Degeneration, Autosomal Dominant 2 44 1.468
223
c HYP331 Hyperphenylalaninemia, Bh4-Deficient, a 59 1.454
224
MSC007 Muscle Hypertrophy 64 1.436
225
SVR004 Severe Combined Immunodeficiency 70 1.436
226
AGR002 Agoraphobia 45 1.428
227
c CHR684 Chronic Kidney Disease 73 1.425
228
OPD006 Opioid Addiction 48 1.419
229
TRN015 Transient Cerebral Ischemia 62 1.417
230
MTR002 Mitral Valve Insufficiency 51 1.415
231
NRL008 Neural Crest Tumor 26 1.403
232
CMP010 Complex Regional Pain Syndrome 59 1.400
233
MCS002 Mucositis 55 1.398
234
MLG169 Malignant Astrocytoma 57 1.392
235
DFC004 Deficiency Anemia 74 1.391
236
DWN001 Down Syndrome 70 1.391
237
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 1.391
238
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 1.384
239
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 1.384
240
GLB002 Glioblastoma 67 1.361
241
STT001 Status Epilepticus 58 1.361
242
PLM033 Pulmonary Embolism 58 1.352
243
CHR344 Chronic Orthostatic Intolerance 13 1.351
244
OST012 Osteoarthritis 77 1.347
245
HRW001 Hair Whorl 35 1.347
246
c NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 66 1.340
247
MRP001 Morphine Dependence 41 1.336
248
P MVM001 Movement Disease 61 1.334
249
c MCL013 Mucolipidosis Iv 64 1.333
250
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 1.333
251
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 1.333
252
SPN031 Supine Hypotensive Syndrome 31 1.333
253
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 40 1.333
254
ATX019 Ataxia with Vitamin E Deficiency 44 1.333
255
HYP020 Hyperprolactinemia 63 1.313
256
TBC004 Tobacco Addiction 63 1.311
257
PLC005 Placental Insufficiency 55 1.309
258
P MTR012 Mitral Valve Disease 57 1.309
259
CRC006 Carcinoid Syndrome 55 1.309
260
P ART018 Aortic Valve Insufficiency 52 1.307
261
ANH002 Anhidrosis 45 1.303
262
P MLT074 Multiple Endocrine Neoplasia 58 1.293
263
P PLY019 Polyneuropathy 52 1.293
264
ANV001 Anovulation 46 1.291
265
ATY001 Atypical Depressive Disorder 45 1.289
266
OCL010 Ocular Hypotension 37 1.285
267
BNR002 Bone Resorption Disease 47 1.281
268
LMB062 Limb Ischemia 55 1.281
269
P MLG056 Malignant Hyperthermia 65 1.271
270
INT007 Intermediate Coronary Syndrome 53 1.271
271
MYC005 Myocardial Stunning 45 1.270
272
THY029 Thyroid Carcinoma 55 1.270
273
P INF032 Infertility 60 1.265
274
c PLM164 Pulmonary Hypertension, Primary, 1 75 1.262
275
P CYS018 Cystitis 58 1.250
276
P DBT005 Diabetes Insipidus 54 1.248
277
HMN044 Human Immunodeficiency Virus Type 1 76 1.235
278
P CRC039 Coarctation of Aorta 46 1.222
279
P AMY004 Amyloidosis 69 1.222
280
c ACT027 Acute Pancreatitis 60 1.218
281
PRT251 Proteinuria, Chronic Benign 58 1.197
282
NRN004 Neuroendocrine Tumor 55 1.194
283
c CNG006 Congenital Hypothyroidism 63 1.192
284
P TCD001 Tic Disorder 50 1.189
285
PST053 Postherpetic Neuralgia 39 1.183
286
P RTT002 Rett Syndrome 79 1.178
287
ANR040 Aneurysm 60 1.178
288
PNS018 Pain Sensitivity Quantitative Trait Locus 1 23 1.177
289
DBT084 Diabetes Mellitus, Ketosis-Prone 59 1.176
290
RLP002 Relapsing-Remitting Multiple Sclerosis 56 1.173
291
P MTR003 Mitral Valve Stenosis 53 1.173
292
PST021 Postpartum Depression 50 1.173
293
c AMY091 Amyotrophic Lateral Sclerosis 1 87 1.169
294
P LTR001 Lateral Sclerosis 57 1.169
295
PRN009 Paranoid Schizophrenia 49 1.169
296
INS023 Insensitivity to Pain, Congenital, with Anhidrosis 56 1.160
297
THY111 Thyroid Carcinoma, Familial Medullary 67 1.159
298
THY125 Thyroid Gland Medullary Carcinoma 48 1.159
299
DSS008 Disease of Mental Health 74 1.159
300
FNT004 Fainting 29 1.152
301
P SLM003 Salmonellosis 54 1.149
302
OCL052 Ocular Dominance 40 1.135
303
OVR094 Ovarian Epithelial Cancer 39 1.129
304
HLX001 Helix Syndrome 47 1.126
305
DBT002 Diabetic Autonomic Neuropathy 40 1.126
306
PHC017 Pheochromocytoma--Islet Cell Tumor Syndrome 18 1.122
307
SPR068 Sporadic Pheochromocytoma/secreting Paraganglioma 29 1.122
308
NNF008 Non-Functioning Paraganglioma 20 1.122
309
PPL052 Papillomatosis, Confluent and Reticulated 34 1.118
310
SHW001 Shwartzman Phenomenon 36 1.118
311
P HYD006 Hydrocephalus 62 1.118
312
P OBS001 Obstructive Jaundice 49 1.117
313
P MGR001 Migraine Without Aura 48 1.117
314
P RSP003 Respiratory Failure 73 1.106
315
P NRV007 Nervous System Disease 65 1.105
316
P ART022 Arthritis 70 1.104
317
CHL068 Cholestasis 61 1.102
318
c PCH010 Pachyonychia Congenita 3 43 1.095
319
CRN017 Coronary Thrombosis 46 1.094
320
P PRS040 Prostate Cancer 95 1.091
321
RPD005 Rapidly Involuting Congenital Hemangioma 48 1.086
322
PRM003 Premature Ejaculation 44 1.086
323
P ART021 Arteriosclerosis 53 1.083
324
HYP781 Hypoascorbemia 52 1.078
325
CRH001 Crohn's Disease 80 1.078
326
P BLD134 Bladder Cancer 79 1.077
327
c BPL002 Bipolar I Disorder 47 1.077
328
HRP004 Herpes Zoster 60 1.077
329
CRB086 Cerebral Aneurysms 40 1.070
330
c HYP724 Hyperlipoproteinemia, Type Iii 66 1.069
331
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 1.069
332
VCC001 Vaccinia 49 1.057
333
ARM002 Aromatic L-Amino Acid Decarboxylase Deficiency 55 1.057
334
HRT012 Heart Valve Disease 53 1.052
335
RYN001 Raynaud Disease 49 1.047
336
c GRV008 Graves Disease 1 54 1.034
337
VSC002 Vascular Dementia 59 1.034
338
c ART101 Aortic Valve Disease 2 65 1.034
339
P ATN002 Autonomic Nervous System Disease 51 1.034
340
NWB001 Newborn Respiratory Distress Syndrome 56 1.031
341
P SCL018 Scoliosis 57 1.030
342
P ART023 Arthropathy 59 1.030
343
P DRM053 Dermatitis, Atopic 65 1.029
344
LPD008 Lipid Metabolism Disorder 61 1.021
345
DRM006 Dermatitis 61 1.013
346
APH002 Aphasia 55 1.012
347
P MLN007 Male Infertility 56 1.012
348
PHB001 Phobic Disorder 45 1.012
349
MNR012 Meniere Disease 55 1.011
350
ACT058 Active Peptic Ulcer Disease 55 1.007
351
LNG099 Lung Disease 62 1.007
352
GST050 Gastrointestinal System Disease 55 1.007
353
FTT001 Fatty Liver Disease 61 1.005
354
SCH012 Schizoaffective Disorder 49 0.995
355
ANR004 Anuria 44 0.995
356
CRB004 Cerebral Artery Occlusion 45 0.994
357
c PRG018 Paragangliomas 1 59 0.992
358
LMY002 Leiomyoma 51 0.984
359
TRD006 Tardive Dyskinesia 53 0.981
360
BCT022 Bacterial Infectious Disease 55 0.973
361
CRD223 Cardiac Arrhythmia 63 0.967
362
c THY107 Thymoma, Familial 42 0.962
363
CRD001 Cardiac Tamponade 44 0.962
364
P THY023 Thymoma 64 0.962
365
P OVR046 Ovarian Cyst 43 0.962
366
VNH007 Von Hippel-Lindau Syndrome 72 0.952
367
P HYP069 Hyperparathyroidism 62 0.952
368
SDD001 Sudden Infant Death Syndrome 60 0.950
369
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.950
370
PTH003 Pathologic Nystagmus 52 0.950
371
HYP835 Hypothalamic Obesity 38 0.950
372
P BRB001 Beriberi 44 0.938
373
GRW007 Growth Hormone Deficiency 47 0.938
374
c NNS018 Nonsyndromic Paraganglioma 33 0.935
375
c ACT134 Acute Liver Failure 57 0.933
376
BCK006 Back Pain 43 0.926
377
P ART005 Arteriovenous Malformation 64 0.926
378
c MJR008 Major Affective Disorder 2 34 0.922
379
c MJR006 Major Affective Disorder 5 32 0.922
380
c MJR003 Major Affective Disorder 6 32 0.922
381
KRT002 Keratomalacia 54 0.922
382
SYS003 Systolic Heart Failure 49 0.914
383
PHY002 Physical Disorder 40 0.913
384
BLR008 Bilirubin Metabolic Disorder 57 0.913
385
IRN001 Iron Deficiency Anemia 58 0.913
386
BRD004 Borderline Personality Disorder 53 0.913
387
PLC008 Placenta Disease 48 0.913
388
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.906
389
P TMP001 Temporal Lobe Epilepsy 49 0.906
390
SPS057 Spasticity 43 0.906
391
NTR005 Nutritional Deficiency Disease 60 0.899
392
INT030 Intracranial Aneurysm 55 0.899
393
P BNC003 Bone Cancer 58 0.899
394
P GLL022 Guillain-Barre Syndrome 59 0.899
395
ATH013 Atherosclerosis Susceptibility 63 0.898
396
P HNT016 Huntington Disease 73 0.890
397
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.890
398
CRN030 Coronary Stenosis 50 0.890
399
OCL006 Ocular Hypertension 53 0.890
400
P ACT105 Acute Mountain Sickness 52 0.890
401
P SCK002 Sick Sinus Syndrome 55 0.884
402
P MLN008 Melanoma 75 0.884
403
ANT024 Anthrax Disease 57 0.884
404
P HYP750 Hypertriglyceridemia, Familial 61 0.881
405
EXT054 Extra-Adrenal Pheochromocytoma 31 0.881
406
PRM020 Premenstrual Tension 39 0.881
407
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.873
408
RFL001 Reflex Sympathetic Dystrophy 51 0.873
409
P HYP050 Hyperinsulinemic Hypoglycemia 56 0.873
410
ALG001 Algoneurodystrophy 37 0.873
411
P ANR048 Aniridia 1 66 0.863
412
P CNR004 Cone-Rod Dystrophy 2 74 0.863
413
CHR682 Chronic Bilirubin Encephalopathy 37 0.863
414
SDD004 Sudden Arrhythmia Death Syndrome 22 0.863
415
SNS003 Sensory Peripheral Neuropathy 51 0.859
416
HYP540 Hypertension, Diastolic 38 0.855
417
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.855
418
P PHC019 Pheochromocytoma-Paraganglioma 35 0.855
419
P HYP263 Hypersomnia 40 0.855
420
ORL015 Oral Squamous Cell Carcinoma 43 0.846
421
P TTR001 Tetralogy of Fallot 69 0.846
422
c MCR115 Microvascular Complications of Diabetes 5 65 0.846
423
c MLG069 Malignant Hypertension 46 0.846
424
CHR074 Choriocarcinoma 46 0.846
425
DRG003 Drug Dependence 46 0.846
426
P MYP004 Myopathy 67 0.836
427
AND020 Androgen Insensitivity, Partial 54 0.836
428
ATX049 Ataxia with Vitamin 3 Deficiency 52 0.836
429
DNT045 Dental Anomalies and Short Stature 50 0.836
430
c MJR023 Major Affective Disorder 7 33 0.836
431
c INF145 Infantile Liver Failure Syndrome 1 44 0.836
432
c MJR004 Major Affective Disorder 4 28 0.836
433
MYF001 Myofibroma 42 0.836
434
OBS003 Obsessive-Compulsive Personality Disorder 43 0.836
435
APP008 Appendicitis 62 0.836
436
HMP028 Hemophagocytic Syndrome Associated with an Infection 24 0.836
437
P ALP009 Alopecia Areata 59 0.836
438
P NSP012 Nasopharyngeal Carcinoma 60 0.834
439
P LNG032 Lung Cancer 98 0.834
440
P OPT006 Optic Nerve Disease 57 0.834
441
EXR010 Exercise-Induced Bronchoconstriction 34 0.827
442
GST033 Gestational Diabetes 60 0.827
443
P MNN013 Meningitis 65 0.827
444
ART016 Aortic Aneurysm 68 0.817
445
P NRF002 Neurofibromatosis 60 0.817
446
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.806
447
ACR007 Acromegaly 70 0.806
448
HYP014 Hyperuricemia 51 0.806
449
c BCT007 Bacterial Meningitis 55 0.806
450
CLT003 Colitis 63 0.796
451
CYS001 Cystic Fibrosis 77 0.796
452
MTH009 Mouth Disease 57 0.796
453
P OPN001 Open-Angle Glaucoma 55 0.796
454
P MSC005 Muscular Dystrophy 66 0.796
455
PRK102 Parkinsonism-Dystonia, Infantile, 2 26 0.794
456
WTR001 Waterhouse-Friderichsen Syndrome 35 0.787
457
P HML002 Hemolytic Anemia 62 0.785
458
SKN016 Skin Disease 63 0.785
459
P THR014 Thrombocytopenia 66 0.774
460
ALC010 Alcoholic Cardiomyopathy 42 0.774
461
ALL014 Allergic Encephalomyelitis 34 0.774
462
THY116 Thyroid Carcinoma, Nonmedullary, with or Without Cell Oxyphilia 17 0.763
463
KRT019 Keratitis, Hereditary 66 0.763
464
STF001 Stiff-Person Syndrome 57 0.763
465
c HPT001 Hepatitis C 61 0.763
466
CSL001 Causalgia 44 0.762
467
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 0.750
468
P GRF003 Graft-Versus-Host Disease 71 0.750
469
P NPH012 Nephrotic Syndrome 61 0.750
470
HND002 Hand, Foot and Mouth Disease 50 0.750
471
PSD088 Pseudobulbar Affect 33 0.750
472
CYN002 Cyanosis, Transient Neonatal 43 0.738
473
CRT069 Cortical Malformations, Occipital 31 0.738
474
HYP114 Hypertensive Nephropathy 35 0.738
475
c DPH024 Diaphragmatic Hernia, Congenital 63 0.738
476
ATM095 Autoimmune Disease 61 0.738
477
OVR063 Overnutrition 42 0.738
478
AMN001 Amenorrhea 53 0.738
479
HYP006 Hypertensive Heart Disease 48 0.738
480
HMP005 Hemiplegia 53 0.738
481
P MCR010 Microcephaly 59 0.738
482
DCB001 Decubitus Ulcer 61 0.738
483
CLB010 Coloboma of Macula 53 0.724
484
c SCL052 Scleroderma, Familial Progressive 60 0.724
485
c SPH013 Spherocytosis, Type 1 42 0.724
486
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 0.724
487
c SPH014 Spherocytosis, Type 2 38 0.724
488
P LPR021 Leprosy 3 71 0.724
489
c THR092 Thrombophilia Due to Thrombin Defect 74 0.724
490
PLC006 Placental Choriocarcinoma 38 0.724
491
P RHN004 Rhinitis 56 0.724
492
DMP001 Dumping Syndrome 43 0.724
493
HNS001 Hansen's Disease 32 0.724
494
c GLC092 Glaucoma, Primary Open Angle 60 0.711
495
P RST001 Restless Legs Syndrome 52 0.711
496
P BRG001 Brugada Syndrome 69 0.711
497
NNL006 Non-Alcoholic Steatohepatitis 54 0.711
498
DPR002 Depersonalization Disorder 41 0.711
499
P GLM007 Glomerulonephritis 59 0.711
500
P BCL017 B-Cell Lymphoma 57 0.711
501
CHR178 Chromosomal Triplication 33 0.711
502
P RRT020 Rare Tumor 39 0.711
503
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.708
504
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.697
505
P INF037 Inflammatory Bowel Disease 53 0.696
506
IMM167 Immune Deficiency Disease 76 0.696
507
OST003 Osteonecrosis 60 0.696
508
SPP007 Suppression Amblyopia 38 0.696
509
AMB002 Amblyopia 49 0.696
510
DBT004 Diabetic Polyneuropathy 50 0.696
511
GT001 Gout 63 0.696
512
PNM013 Pneumococcal Meningitis 43 0.696
513
ALX002 Alexithymia 36 0.680
514
P VNS003 Venous Insufficiency 54 0.680
515
CHR431 Chronic Venous Insufficiency 48 0.680
516
P LMY004 Leiomyosarcoma 62 0.680
517
P OVR049 Ovarian Disease 50 0.680
518
PLM001 Pulmonary Tuberculosis 69 0.680
519
BRN036 Brain Stem Infarction 38 0.680
520
GTR002 Goiter 52 0.680
521
P HYP083 Hypopituitarism 51 0.680
522
NRL005 Neurilemmoma 60 0.664
523
P HRN001 Horner's Syndrome 45 0.664
524
LYD001 Leydig Cell Tumor 45 0.664
525
c JVN010 Juvenile Rheumatoid Arthritis 52 0.664
526
CHC001 Chickenpox 56 0.664
527
c ACT135 Acute Graft Versus Host Disease 51 0.664
528
ARG004 Argyria 26 0.664
529
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.664
530
WRN002 Wernicke-Korsakoff Syndrome 49 0.645
531
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 47 0.645
532
P LNG064 Lung Cancer Susceptibility 3 69 0.645
533
RTN020 Retinal Vascular Disease 45 0.645
534
P PYL005 Pyelonephritis 56 0.645
535
PST011 Pustulosis of Palm and Sole 52 0.645
536
c ACT076 Acute Myocarditis 46 0.645
537
c ACT068 Acute Cystitis 60 0.645
538
P CMP008 Compartment Syndrome 49 0.645
539
BRN056 Bronchopulmonary Dysplasia 57 0.645
540
P PSR002 Psoriasis 63 0.645
541
PLC007 Placental Abruption 47 0.645
542
CNT015 Central Sleep Apnea 46 0.636
543
ALL003 Allergic Rhinitis 66 0.625
544
SNT005 Sinoatrial Node Disease 48 0.625
545
c DYS191 Dystonia 1, Torsion, Autosomal Dominant 47 0.625
546
GLC096 Galactorrhea 40 0.625
548
WLS001 Wilson Disease 70 0.625
549
ATS010 Autosomal Recessive Disease 42 0.625
550
IFP003 Ifap Syndrome 2 41 0.625
551
FDB001 Foodborne Botulism 55 0.625
552
BRK010 Burkitt Lymphoma 65 0.625
553
SBJ001 Subjective Cognitive Decline 29 0.625
554
ACT078 Acute Porphyria 50 0.625
555
HMN009 Hemangioblastoma 53 0.625
556
c CNT035 Central Nervous System Disease 53 0.625
557
P ANT001 Anterolateral Myocardial Infarction 34 0.625
558
c ATM022 Autoimmune Myocarditis 35 0.625
559
P PRP029 Porphyria 60 0.625
560
P PLM036 Pulmonary Fibrosis 65 0.625
561
ALC006 Alcoholic Hepatitis 61 0.625
562
RTN003 Retinal Ischemia 48 0.625
563
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.625
564
INF118 Inflammatory Myopathy with Abundant Macrophages 27 0.625
565
c AMY009 Amyloidosis Aa 47 0.625
566
MST020 Mast Cell Activation Syndrome 27 0.625
567
SPL018 Splenomegaly 47 0.625
568
P OST002 Osteoporosis 76 0.608
569
P AST005 Asthma 75 0.608
570
NCL008 Nuclear Ribonucleic Acid 15 0.602
571
c BRG008 Brugada Syndrome 6 32 0.602
572
P TRT019 Torticollis 47 0.602
573
MYL069 Myeloma, Multiple 76 0.602
574
c DMN023 Diamond-Blackfan Anemia 1 68 0.602
575
ISL003 Isolated Growth Hormone Deficiency 56 0.602
576
CCC002 Coccidiosis 50 0.602
577
NRT004 Neuritis 53 0.602
578
RTR007 Retroperitoneal Leiomyosarcoma 27 0.602
579
P BLP003 Blepharospasm 45 0.602
580
CRT008 Carotid Artery Dissection 29 0.602
581
P THY032 Thyroiditis 56 0.602
582
DST006 Diastolic Heart Failure 45 0.602
583
PRN061 Prenatal-Onset Spinal Muscular Atrophy with Congenital Bone Fractures 13 0.602
584
ACQ007 Acquired Immunodeficiency Syndrome 58 0.592
585
ALL006 Allergic Asthma 55 0.592
586
P HRD021 Hereditary Sensory Neuropathy 48 0.582
587
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.576
588
P MGR003 Migraine with Aura 51 0.576
589
SQM006 Squamous Cell Carcinoma 59 0.576
590
CRT013 Carotid Stenosis 51 0.576
591
WHP002 Whiplash 35 0.576
592
c SYS001 Systemic Lupus Erythematosus 85 0.575
593
c SML038 Small Cell Cancer of the Lung 68 0.575
594
c ART112 Arthrogryposis, Distal, Type 10 36 0.575
595
KWS002 Kawasaki Disease 65 0.575
596
PRS064 Persistent Vegetative State 33 0.575
597
BRN014 Bronchopneumonia 52 0.575
598
VSC004 Vasculogenic Impotence 29 0.575
599
PTT009 Pituitary Gland Disease 52 0.575
600
GST040 Gastric Adenocarcinoma 66 0.575
601
P EPS003 Episodic Ataxia 59 0.575
602
P LPS004 Lupus Erythematosus 61 0.575
603
SHP003 Shapiro Syndrome 25 0.575
604
ACT235 Acute Macular Neuroretinopathy 16 0.575
605
c ACT150 Acute Adrenal Insufficiency 48 0.575
606
MYT011 Myotonia 37 0.575
607
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 0.575
608
P PRV006 Pervasive Developmental Disorder 52 0.557
609
IDP070 Idiopathic Scoliosis 41 0.540
610
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.540
611
OTS013 Otospondylomegaepiphyseal Dysplasia, Autosomal Recessive 56 0.540
612
PHS025 Phosphatase, Acid, of Tissues 28 0.540
613
ANG020 Angiosarcoma 63 0.540
614
MND023 Mend Syndrome 49 0.540
615
IGR001 Ige Responsiveness, Atopic 58 0.540
616
c MST023 Mesothelioma, Malignant 56 0.540
617
c ATM102 Autoimmune Cardiomyopathy 30 0.540
618
P BNG032 Benign Mesothelioma 53 0.540
619
NRM004 Neuroma 49 0.540
620
OCL004 Ocular Hyperemia 24 0.540
621
ART017 Aortic Disease 49 0.540
622
P CND004 Candidiasis 57 0.540
623
INT078 Intracranial Thrombosis 50 0.540
624
DBT008 Diabetic Angiopathy 47 0.540
625
P FML340 Familial Episodic Pain Syndrome 50 0.540
626
HYP057 Hypervitaminosis D 37 0.540
627
MNN020 Meningococcal Infection 44 0.540
628
MNN021 Meningococcemia 34 0.540
629
HRN003 Heroin Dependence 44 0.540
630
OPD001 Opioid Abuse 44 0.537
631
ENT004 Enthesopathy 51 0.537
632
P PRD008 Periodontitis 63 0.537
633
IDP033 Idiopathic Edema 41 0.537
634
VRS002 Virus-Associated Trichodysplasia Spinulosa 30 0.537
635
INT146 Intervertebral Disc Disease 61 0.514
636
LPT014 Leptin Deficiency or Dysfunction 77 0.514
637
ESP021 Esophageal Cancer 84 0.514
638
P CNJ013 Conjunctivitis 66 0.514
639
TXC002 Toxic Encephalopathy 51 0.514
640
INS024 Insulin-Like Growth Factor I 77 0.505
641
c NRP037 Neuropathy, Hereditary Sensory and Autonomic, Type V 56 0.497
642
MLD017 Mal De Debarquement Syndrome 33 0.497
643
BDY001 Body Dysmorphic Disorder 40 0.487
644
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.487
645
SMT006 Somatoform Disorder 50 0.487
646
P ESP024 Esophagitis 60 0.487
647
PRS047 Prostatitis 57 0.487
648
CNN001 Cannabis Dependence 37 0.487
649
SPN092 Spinal Shock 20 0.487
651
c HPT016 Hepatitis B 62 0.454
652
RHM001 Rheumatic Fever 59 0.454
653
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 0.452
654
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.452
655
P FNG006 Feingold Syndrome 1 61 0.452
656
EPT021 Epithelial Recurrent Erosion Dystrophy 45 0.452
657
c PRD040 Periodontitis, Chronic 52 0.452
658
c BRN108 Branchiootic Syndrome 1 63 0.452
659
HPT085 Hepatitis, Fulminant Viral 33 0.452
660
CNT097 Central Hypoventilation Syndrome, Congenital 70 0.452
661
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 67 0.452
662
c DYS119 Dystonia 9 54 0.452
663
SCH003 Schizophreniform Disorder 54 0.452
664
BLD051 Blood Coagulation Disease 52 0.452
665
GNG013 Gingivitis 59 0.452
666
BLR004 Biliary Dyskinesia 37 0.452
667
PRD004 Prediabetes Syndrome 52 0.452
668
DGN001 Degenerative Disc Disease 48 0.452
669
c PRM038 Primary Agammaglobulinemia 47 0.452
670
TMP019 Temporomandibular Joint Anomaly 28 0.452
671
PHN003 Phenylketonuria 76 0.444
672
P CLS010 Cluster Headache 42 0.435
673
HRT011 Heart Septal Defect 49 0.427
674
ADN018 Adenoma 58 0.427
675
P DRR001 Diarrhea 55 0.418
676
MTN003 Motion Sickness 50 0.410
677
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 33 0.401
678
PRP027 Peripheral Vascular Disease 71 0.401
679
P EXN002 Exanthem 58 0.401
680
P HYP265 Hypotonia 42 0.401
681
ART002 Arts Syndrome 66 0.391
682
P GRV001 Graves' Disease 54 0.382
683
QDR001 Quadriplegia 49 0.382
684
c PRM005 Primary Hyperparathyroidism 59 0.382
685
P LNG028 Long Qt Syndrome 63 0.372
686
PRP016 Paraplegia 52 0.372
687
RTR001 Retrograde Amnesia 41 0.372
688
LWC001 Low Compliance Bladder 44 0.372
689
PST092 Posttransplant Acute Limbic Encephalitis 29 0.372
690
c BNM021 Bone Mineral Density Quantitative Trait Locus 7 12 0.366
691
OST062 Osteoarthritis with Mild Chondrodysplasia 46 0.366
692
PRP001 Propionic Acidemia 65 0.366
693
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.366
694
EHL052 Ehlers-Danlos Syndrome, Vascular Type 63 0.366
695
P PHT010 Photoparoxysmal Response 1 46 0.366
696
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 0.366
697
SPP011 Suppression of Tumorigenicity 12 61 0.366
698
c PRS130 Prostate Cancer, Hereditary, 8 32 0.366
699
P ASP001 Asperger Syndrome 48 0.366
700
PTC002 Potocki-Lupski Syndrome 51 0.366
701
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 44 0.366
702
AMD002 Amed Syndrome, Digenic 36 0.366
703
ANG049 Angioedema Induced by Ace Inhibitors 38 0.366
704
NRP027 Neuropathy, Painful 21 0.366
705
ENH001 Enhanced S-Cone Syndrome 58 0.366
706
P MCR384 Microcephaly, Epilepsy, and Diabetes Syndrome 1 41 0.366
707
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.366
708
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 38 0.366
709
LPT006 Leptin Receptor Deficiency 50 0.366
710
SCR035 Sacral Agenesis with Vertebral Anomalies 38 0.366
711
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.366
712
c BLD140 Blood Group, I System 47 0.366
713
IMM162 Immunoglobulin E Concentration, Serum 28 0.366
714
c FNC043 Fanconi Anemia, Complementation Group E 62 0.366
715
P KHL003 Kohlschutter-Tonz Syndrome 57 0.366
716
c PRS136 Prostate Cancer, Hereditary, 6 33 0.366
717
SPN369 Spinal Disease 43 0.366
718
ACT011 Acute Contagious Conjunctivitis 41 0.366
719
CHL159 Childhood-Onset Asthma 30 0.366
720
P END084 Endocrine System Disease 44 0.366
721
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 38 0.366
722
URT001 Urethritis 52 0.366
723
GST071 Gastrointestinal Carcinoma 46 0.366
724
ANL018 Analbuminemia 53 0.366
725
TWN001 Twin-to-Twin Transfusion Syndrome 45 0.366
726
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.366
727
PHT003 Phototoxic Dermatitis 27 0.366
728
PLM022 Pulmonary Valve Insufficiency 45 0.366
729
BRN038 Bronchial Disease 51 0.366
730
SMT001 Somatization Disorder 49 0.366
731
P CRV039 Cervicitis 52 0.366
732
P ADN016 Adenocarcinoma 63 0.366
733
P AGN002 Agnosia 53 0.366
734
GST049 Gastrointestinal System Cancer 49 0.366
735
LRY018 Laryngeal Squamous Cell Carcinoma 47 0.366
736
VSL002 Visual Epilepsy 39 0.366
737
P INT070 Intestinal Obstruction 57 0.366
738
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 50 0.366
739
SPN027 Spinal Stenosis 58 0.366
740
NRN002 Neuronitis 31 0.366
741
CNN002 Cannabis Abuse 44 0.366
742
CYS021 Cystic Adenomatoid Malformation of Lung 33 0.366
743
CYT018 Cytochrome P450 2d6 Variant 26 0.366
744
VLV042 Vulvar Vestibulitis Syndrome 39 0.366
746
END072 Endotheliitis 36 0.366
747
CTS005 Catastrophic Antiphospholipid Syndrome 43 0.366
748
CHL079 Children's Interstitial Lung Disease 25 0.366
750
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.366
751
CRB079 Cerebrospinal Fluid Leak 35 0.366
752
MNK001 Menkes Disease 64 0.362
753
c MCR133 Microvascular Complications of Diabetes 4 41 0.362
754
c MCR113 Microvascular Complications of Diabetes 3 52 0.362
755
c MCR130 Microvascular Complications of Diabetes 6 41 0.362
756
c MCR120 Microvascular Complications of Diabetes 7 47 0.362
757
c PRG042 Progressive Familial Heart Block, Type Ia 65 0.362
758
HYP141 Hyperphenylalaninemia 42 0.362
759
BRR004 Baroreflex Failure 21 0.362
760
PTT037 Pituitary Tumors 44 0.352
761
P HRP006 Herpes Simplex 65 0.352
762
SCR039 Scorpion Envenomation 42 0.352
763
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.342
764
CNN003 Conn's Syndrome 77 0.342
765
CND002 Conduct Disorder 50 0.342
766
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.331
767
OVR029 Ovarian Hyperstimulation Syndrome 63 0.331
768
P ATR010 Atrial Heart Septal Defect 58 0.331
769
GST037 Gastroparesis 52 0.331
770
INS001 Insulinoma 59 0.331
771
P MSC003 Muscular Atrophy 52 0.331
772
P MYC033 Myoclonus 46 0.331
773
ACT088 Acute Insulin Response 39 0.320
774
P DXT004 Dextro-Looped Transposition of the Great Arteries 58 0.320
775
PTH002 Pathological Gambling 48 0.320
776
AVD001 Avoidant Personality Disorder 49 0.320
777
HMC014 Homocysteinemia 52 0.308
778
EWN003 Ewing Sarcoma 69 0.308
779
TRG002 Trigeminal Neuralgia 61 0.308
780
P HYP120 Hypoaldosteronism 33 0.308
781
ORL012 Oral Leukoplakia 35 0.308
782
LKP003 Leukoplakia 39 0.308
783
LPD012 Lipoid Congenital Adrenal Hyperplasia 68 0.296
784
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.296
785
DSS032 Disease by Infectious Agent 55 0.296
786
GST023 Gastric Ulcer 52 0.296
787
LYM027 Lymphopenia 56 0.296
788
c SCN007 Secondary Hyperparathyroidism 50 0.296
789
P ENC004 Encephalitis 61 0.296
790
P PLY018 Polycythemia 56 0.296
791
ATM074 Autoimmune Autonomic Ganglionopathy 19 0.296
792
RNL077 Renal Fibrosis 46 0.283
793
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.283
794
FML063 Familial Glucocorticoid Deficiency 58 0.283
795
RCK004 Rickets 64 0.283
796
ILS001 Ileus 49 0.283
797
PRP007 Priapism 46 0.283
798
GNT167 Genetic Obesity 33 0.283
799
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.270
800
OST159 Osteogenic Sarcoma 66 0.270
801
LSC001 Lesch-Nyhan Syndrome 62 0.270
802
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 0.270
803
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.270
804
P TMR010 Tumor Predisposition Syndrome 69 0.270
805
DSS009 Disseminated Intravascular Coagulation 56 0.270
806
c ACT249 Acute Asthma 40 0.270
807
P VNT002 Ventricular Septal Defect 58 0.270
808
GLM008 Glomus Tumor 48 0.270
809
P PTT006 Pituitary Adenoma 55 0.270
810
CHR073 Choreatic Disease 53 0.270
811
ACT003 Acute Kidney Tubular Necrosis 46 0.270
812
RGH001 Right Bundle Branch Block 47 0.270
813
c SVR005 Severe Pre-Eclampsia 49 0.270
814
INH023 Inherited Cancer-Predisposing Syndrome 53 0.270
815
ADR041 Adrenal Cortical Adenoma 48 0.256
816
c PRM093 Premature Ovarian Failure 7 47 0.256
817
FCL014 Focal Epilepsy 53 0.256
818
GNG005 Gangliocytoma 54 0.256
819
GNG002 Ganglioneuroma 52 0.256
820
P END033 Endocarditis 58 0.256
821
CRN036 Craniopharyngioma 63 0.256
822
PLY100 Polyploidy 36 0.256
823
MNG007 Manganese Poisoning 28 0.256
824
MLT116 Multiple System Atrophy, Parkinsonian Type 29 0.256
825
INF034 Infective Endocarditis 53 0.242
826
OPP004 Oppositional Defiant Disorder 48 0.242
827
P HYP605 Hyperphenylalaninemia, Bh4-Deficient, B 44 0.242
828
GST092 Gastroesophageal Reflux 59 0.242
829
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 0.242
830
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.242
831
CLN015 Colon Adenocarcinoma 64 0.242
832
CHL067 Cholecystitis 59 0.242
833
P ACN011 Acne 55 0.242
834
RYS001 Reye Syndrome 49 0.242
835
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.242
836
MYM001 Myoma 54 0.242
837
c ESS001 Essential Tremor 56 0.242
838
HYP043 Hyperandrogenism 47 0.242
839
PRC013 Pericarditis 53 0.242
840
P CTR002 Cataract 59 0.242
841
BP1002 Bap1 Tumor Predisposition Syndrome 42 0.242
842
PPT005 Peptic Ulcer Disease 58 0.242
843
P SCK005 Sickle Cell Disease 56 0.242
844
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.226
845
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 0.226
846
PLY150 Polykaryocytosis Inducer 29 0.226
847
MSC157 Muscular Dystrophy, Duchenne Type 78 0.226
848
c PNS012 Paine Syndrome 60 0.226
849
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.226
850
c PRG021 Paragangliomas 4 38 0.226
851
GST019 Gastrointestinal Stromal Tumor 78 0.226
852
ANS021 Anisocoria 24 0.226
853
DYS192 Dystonia, Dopa-Responsive 56 0.226
854
P FTL001 Fetal Alcohol Syndrome 55 0.226
855
DNT012 Dental Caries 53 0.226
856
CRB037 Cerebral Palsy 66 0.226
857
CNS002 Constrictive Pericarditis 39 0.226
858
URT010 Ureteral Obstruction 44 0.226
859
ART074 Aortic Dissection 53 0.226
860
NWC001 Newcastle Disease 47 0.226
861
GNG008 Ganglioneuroblastoma 46 0.226
862
c BNG021 Benign Essential Hypertension 37 0.226
863
JPN002 Japanese Encephalitis 61 0.226
864
NSP002 Nasopharyngitis 45 0.226
865
NRL004 Neuroleptic Malignant Syndrome 52 0.226
866
CPL003 Capillary Leak Syndrome 54 0.226
867
P VSC011 Vasculitis 61 0.226
868
P TXP001 Toxoplasmosis 59 0.226
869
TTR011 Tetraploidy 43 0.226
870
PRT256 Portosinusoidal Vascular Disease 9 0.226
871
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.209
872
SCR003 Secretory Diarrhea 35 0.209
873
c FML116 Familial Cold Autoinflammatory Syndrome 1 55 0.209
874
P PTN014 Patent Ductus Arteriosus 1 59 0.209
876
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.209
877
ESP002 Esophageal Varix 51 0.209
878
P HMN010 Hemangioma 61 0.209
879
P TRN020 Turner Syndrome 67 0.209
880
NPH009 Nephrolithiasis 54 0.209
881
SPN035 Spindle Cell Sarcoma 51 0.209
882
BRX001 Bruxism 50 0.209
883
PRN007 Perinephritis 38 0.209
884
CVD001 Covid-19 59 0.209
885
P GND004 Gonadal Dysgenesis 46 0.209
886
SRC014 Sarcoma 64 0.209
887
VRC001 Varicocele 48 0.209
888
RMS001 Rem Sleep Behavior Disorder 47 0.209
889
P RTN016 Retinal Degeneration 52 0.209
890
HMP009 Haemophilus Influenzae 41 0.209
891
ESN011 Eisenmenger Syndrome 46 0.209
892
P MRC003 Mercury Poisoning 48 0.209
893
CRB090 Cerebral Hypoxia 42 0.209
894
MLR004 Malaria 77 0.191
895
P ATR001 Atrioventricular Septal Defect 54 0.191
896
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.191
897
c ART115 Aortic Valve Disease 1 72 0.191
898
LPM012 Lipomatosis, Multiple 59 0.191
899
PLM061 Pulmonary Edema of Mountaineers 25 0.191
900
SCK003 Sickle Cell Anemia 74 0.191
901
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.191
902
ASP026 Asplenia, Isolated Congenital 43 0.191
903
ENT011 Enterocolitis 55 0.191
904
P MYS003 Myasthenia Gravis 67 0.191
905
c HYP368 Hyperphenylalaninemia, Bh4-Deficient, C 35 0.191
906
FRN006 Frontotemporal Dementia 68 0.191
907
CHR005 Chorioamnionitis 50 0.191
908
OBS082 Obstructive Nephropathy 41 0.191
909
P MYG005 Myoglobinuria 40 0.191
910
TRY001 Trypanosomiasis 50 0.191
911
PLM005 Pleomorphic Lipoma 39 0.191
912
ANT011 Antisocial Personality Disorder 47 0.191
913
HYP080 Hypogonadism 49 0.191
914
PNM008 Pneumothorax 54 0.191
915
RHM028 Rheumatic Heart Disease 55 0.191
916
BRN009 Burning Mouth Syndrome 51 0.191
917
ASP004 Asphyxia Neonatorum 50 0.191
918
P BRS044 Breast Adenocarcinoma 58 0.191
919
P STR001 Striatonigral Degeneration 37 0.191
920
NPH010 Nephrosclerosis 50 0.191
921
SCH014 Schistosomiasis 56 0.191
922
OLV001 Olivopontocerebellar Atrophy 50 0.191
923
P URT039 Urticaria 57 0.191
924
HYD002 Hydronephrosis 58 0.191
925
CHL013 Cholecystolithiasis 37 0.191
926
LFT001 Left Bundle Branch Hemiblock 47 0.191
927
BRN024 Bronchitis 67 0.191
928
AMP007 Amphetamine Abuse 36 0.191
929
ACH005 Achalasia 54 0.191
930
PRT029 Parathyroid Adenoma 51 0.191
931
LRN003 Learning Disability 49 0.191
932
SBS004 Substance Dependence 46 0.191
933
NRF007 Neurofibroma 63 0.191
934
PRN019 Perinatal Necrotizing Enterocolitis 60 0.191
935
PYR016 Pyridoxine Deficiency 29 0.191
936
c ERL020 Early-Onset Schizophrenia 43 0.191
937
DSR031 Disorder of Copper Metabolism 25 0.191
938
HYP264 Hypertonia 35 0.191
939
PRS063 Paresthesia 39 0.191
940
SGW002 Segawa Syndrome, Autosomal Recessive 44 0.171
941
c HNT004 Huntington Disease-Like 2 51 0.171
942
SCN049 Second-Degree Atrioventricular Block 34 0.171
943
ASP007 Aspiration Pneumonia 49 0.171
944
P PRD006 Prader-Willi Syndrome 60 0.171
945
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.171
946
GST009 Gastroschisis 53 0.171
947
NRR002 Norrie Disease 59 0.171
948
c PRG019 Paragangliomas 2 30 0.171
949
TRC010 Trichotillomania 51 0.171
950
P GST053 Gastric Cancer 82 0.171