Search results for ache

2079 hits were found for ache

# Family MCID Name MIFTS Score
1
ACH004 Achondroplasia 66 31.683
2
P ALZ034 Alzheimer Disease 87 26.298
3
P MYS003 Myasthenia Gravis 68 20.917
4
YTB001 Yt Blood Group Antigen 9 20.861
5
P NRB001 Neuroblastoma 66 19.558
6
AMN003 Amnestic Disorder 54 17.614
7
P DMN002 Dementia 66 17.139
8
VSC002 Vascular Dementia 60 16.559
9
P CNG001 Congenital Myasthenic Syndrome 68 16.037
10
P HRS035 Hirschsprung Disease 1 66 15.923
11
P MYP004 Myopathy 67 15.758
12
NRL016 Neural Tube Defects 81 15.625
13
AGN016 Aging 54 14.491
14
c TYP009 Type 2 Diabetes Mellitus 92 14.433
15
MLR004 Malaria 80 14.175
16
P PLY019 Polyneuropathy 52 14.069
17
P HNT016 Huntington Disease 73 13.838
18
CRB039 Cerebrovascular Disease 66 13.449
19
P NRP001 Neuropathy 60 13.113
20
P SCH015 Schizophrenia 74 12.998
21
PRT037 Pertussis 65 12.977
22
c MYS051 Myasthenic Syndrome, Congenital, 5 53 12.965
23
P PRK057 Parkinson Disease, Late-Onset 80 12.931
24
ANX010 Anxiety 70 12.859
25
DWN001 Down Syndrome 70 12.842
26
ACH005 Achalasia 55 12.599
27
P RSP003 Respiratory Failure 74 12.414
28
FRN006 Frontotemporal Dementia 68 12.228
29
STT001 Status Epilepticus 59 12.160
30
P DBT009 Diabetes Mellitus 67 12.118
31
WRN002 Wernicke-Korsakoff Syndrome 50 11.429
32
ANN002 Anencephaly 57 11.425
33
P ATS364 Autism 69 11.314
34
P DRR001 Diarrhea 55 11.273
35
CLN006 Colonic Pseudo-Obstruction 30 10.952
36
INT323 Intraocular Pressure Quantitative Trait Locus 64 10.937
37
P SPR120 Supranuclear Palsy, Progressive, 1 69 10.699
38
MGC001 Megacolon 48 10.699
39
TRN015 Transient Cerebral Ischemia 63 10.673
40
DMN031 Dementia, Lewy Body 65 10.514
41
P INT070 Intestinal Obstruction 57 10.276
42
GST009 Gastroschisis 53 10.244
43
PHN003 Phenylketonuria 76 10.143
44
SCR011 Scrapie 39 9.980
45
P OMP004 Omphalocele 48 9.917
46
PCK003 Pick Disease of Brain 69 9.787
47
P PRP019 Peripheral Nervous System Disease 58 9.686
48
INT072 Intestinal Pseudo-Obstruction 62 9.526
49
c CNG006 Congenital Hypothyroidism 63 9.463
50
PSY004 Psychotic Disorder 66 9.320
51
RMS001 Rem Sleep Behavior Disorder 47 9.133
52
NRM005 Neuromuscular Disease 63 9.105
53
c CNG513 Congenital Ptosis 42 9.001
54
SPC010 Speech and Communication Disorders 48 8.682
55
AGR018 Agraphia 37 8.682
56
P JNC001 Junctional Epidermolysis Bullosa 53 8.682
57
HYP572 Hypoganglionosis 27 8.439
58
TND006 Tendinosis 41 8.416
59
PRT058 Pure Autonomic Failure 58 8.008
60
BNS003 Binswanger's Disease 41 7.856
61
DSS008 Disease of Mental Health 74 7.838
62
ANH002 Anhidrosis 46 7.701
63
P ORT004 Orthostatic Intolerance 63 7.635
64
CHL035 Cholinergic Urticaria 29 7.454
65
BTY001 Butyrylcholinesterase Deficiency 49 7.374
66
PRS011 Persian Gulf Syndrome 35 7.147
67
P HDC001 Headache 57 7.090
68
P NRM006 Neuromuscular Junction Disease 34 6.983
69
NRT001 Neurotic Disorder 56 6.852
70
P NRV007 Nervous System Disease 67 6.852
71
APL023 Aplasia Cutis Congenita, Nonsyndromic 46 6.590
72
HYP266 Hypoxia 57 6.554
73
TXC002 Toxic Encephalopathy 52 6.458
74
NRG001 Neurogenic Bowel 31 6.458
75
P PHC003 Pheochromocytoma 69 6.416
76
ADR040 Adrenal Gland Pheochromocytoma 46 6.416
77
THM026 Thiamine Deficiency Disease 24 6.139
78
c EXD006 Exudative Vitreoretinopathy 5 40 6.139
79
c ALZ057 Alzheimer Disease 10 35 6.139
80
SML010 Simultanagnosia 32 6.139
81
ACT018 Acute Laryngopharyngitis 24 6.139
82
NMN001 Nominal Aphasia 40 6.139
83
P PPL023 Pupil Disease 26 6.139
84
CRB016 Carbuncle 39 6.139
85
P PRM227 Primary Orthostatic Hypotension 24 6.139
86
HYP066 Hyperglycemia 61 6.022
87
P ATR011 Atrial Fibrillation 66 5.864
88
PPL052 Papillomatosis, Confluent and Reticulated 34 5.855
89
CNS004 Constipation 56 5.746
90
HLX001 Helix Syndrome 48 5.717
91
P TRM003 Tremor 48 5.605
92
c HYP836 Hypercholesterolemia, Familial, 1 73 5.596
93
HMN044 Human Immunodeficiency Virus Type 1 78 5.324
94
P SZR006 Seizure Disorder 70 4.923
95
RPD005 Rapidly Involuting Congenital Hemangioma 46 4.923
96
BCK006 Back Pain 47 4.909
97
P MSC005 Muscular Dystrophy 67 4.776
98
P CHR345 Chronic Pain 50 4.723
99
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 4.687
100
CHL014 Cholera 62 4.562
101
P EXN002 Exanthem 58 4.488
102
ISC004 Ischemia 61 4.486
103
ACR005 Acrodermatitis 38 4.431
104
P PLM037 Pulmonary Hypertension 72 4.422
105
FBR047 Fibromyalgia 58 4.362
106
LPP008 Lipoprotein Quantitative Trait Locus 65 4.352
107
P HYP086 Hypothyroidism 69 4.343
108
48X005 48,xyyy 39 4.337
109
c AMY091 Amyotrophic Lateral Sclerosis 1 88 4.324
110
P LTR001 Lateral Sclerosis 58 4.324
111
47X002 47,xyy 48 4.295
112
DWR001 Dwarfism 44 4.290
113
IMP005 Impotence 52 4.266
114
HYP042 Hypochondroplasia 59 4.180
115
ART140 Arteries, Anomalies of 53 4.180
116
c HYP595 Hypertension, Essential 85 4.158
117
ANX004 Anoxia 40 4.099
118
c MGR028 Migraine with or Without Aura 1 64 4.042
119
HMG002 Hemoglobinuria 50 4.029
120
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 4.007
121
TTN003 Tetanus 65 3.951
122
P VSC007 Vascular Disease 63 3.905
123
TRM010 Traumatic Brain Injury 51 3.861
124
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 3.855
125
OST012 Osteoarthritis 77 3.772
126
IRR002 Irritable Bowel Syndrome 65 3.772
127
P EPL164 Epilepsy 68 3.765
128
LMB002 Lambert-Eaton Myasthenic Syndrome 52 3.764
129
PNG002 Pain Agnosia 51 3.745
130
SBC016 Subacute Delirium 43 3.705
131
P ANP001 Anaplastic Large Cell Lymphoma 61 3.664
132
P PST059 Pustular Psoriasis 38 3.657
133
SVR001 Severe Acute Respiratory Syndrome 67 3.649
134
c HPT001 Hepatitis C 62 3.595
135
P BPL003 Bipolar Disorder 56 3.582
136
MLD018 Mild Cognitive Impairment 48 3.551
137
HYP060 Hyperinsulinism 54 3.542
138
c HPT073 Hepatitis C Virus 71 3.538
139
c ACT071 Acute Kidney Failure 60 3.528
140
c MJR022 Major Affective Disorder 8 38 3.520
141
c MJR024 Major Affective Disorder 9 41 3.520
142
GLL048 Glial Tumor 52 3.449
143
GLM045 Glioma 63 3.449
144
ATM095 Autoimmune Disease 61 3.446
145
ALL029 Allergic Disease 59 3.436
146
c PRC016 Pre-Eclampsia 65 3.404
147
P INF038 Influenza 68 3.343
148
P HPT021 Hepatitis 69 3.311
149
PST028 Post-Traumatic Stress Disorder 59 3.302
150
SKL017 Skeletal Dysplasias 41 3.298
151
P BRB001 Beriberi 44 3.281
152
P ESP024 Esophagitis 60 3.261
153
PRP027 Peripheral Vascular Disease 71 3.259
154
P PSR002 Psoriasis 63 3.241
155
PST011 Pustulosis of Palm and Sole 52 3.241
156
CHG001 Chagas Disease 66 3.227
157
RCK004 Rickets 68 3.216
158
CRN019 Coronary Artery Vasospasm 47 3.205
159
BRN071 Brain Injury 50 3.205
160
ENT004 Enthesopathy 51 3.203
161
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 3.189
162
c ATR087 Atrial Standstill 1 74 3.146
163
CRT015 Carotid Artery Occlusion 45 3.107
164
P ENC018 Encephalopathy 62 3.107
165
P DYS154 Dystonia 64 3.095
166
ANG054 Angina Pectoris 66 3.075
167
DPR016 Depression 65 3.050
168
P BCL017 B-Cell Lymphoma 59 3.047
169
LWC001 Low Compliance Bladder 45 3.008
170
P INF037 Inflammatory Bowel Disease 53 3.007
171
YLL002 Yellow Fever 61 2.997
172
LPD008 Lipid Metabolism Disorder 62 2.991
173
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 2.986
174
VRC005 Varicose Veins 60 2.986
175
P HYP098 Hypereosinophilic Syndrome 66 2.986
176
P ATS011 Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 48 2.945
177
P VSC011 Vasculitis 61 2.945
178
P THN009 Thanatophoric Dysplasia, Type I 63 2.940
179
PST092 Posttransplant Acute Limbic Encephalitis 28 2.940
180
ACT084 Acute Stress Disorder 54 2.940
181
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 2.924
182
c LKM005 Leukemia, T-Cell, Chronic 34 2.924
183
P RHM011 Rheumatoid Arthritis 82 2.916
184
MDD011 Mood Disorder 62 2.903
185
PLY150 Polykaryocytosis Inducer 29 2.887
186
P ENC004 Encephalitis 61 2.881
187
CLT003 Colitis 63 2.860
188
P ATT013 Attention Deficit-Hyperactivity Disorder 64 2.860
189
DYS073 Dysphagia 53 2.860
190
P TMP003 Temporal Arteritis 69 2.838
191
P MYC007 Myocardial Infarction 70 2.816
192
MTN003 Motion Sickness 51 2.771
193
P AMY004 Amyloidosis 70 2.771
194
SKN016 Skin Disease 63 2.743
195
IMM167 Immune Deficiency Disease 78 2.735
196
c MCR115 Microvascular Complications of Diabetes 5 65 2.726
197
P HYD006 Hydrocephalus 61 2.726
198
P PRK039 Parkinsonism 55 2.724
199
CHK001 Chikungunya 60 2.722
200
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.712
201
CYT002 Cytokine Deficiency 43 2.703
202
P HYP076 Hyperthyroidism 53 2.687
203
P KDN018 Kidney Disease 72 2.679
204
SPN186 Spinal Cord Injury 61 2.668
205
P AST005 Asthma 76 2.668
206
P HYP069 Hyperparathyroidism 62 2.656
207
ATH013 Atherosclerosis Susceptibility 63 2.649
208
P RHN004 Rhinitis 57 2.649
209
PLM129 Pulmonary Disease, Chronic Obstructive 74 2.610
210
OCL069 Ocular Motor Apraxia 57 2.607
211
DBT010 Diabetic Neuropathy 54 2.607
212
CRB037 Cerebral Palsy 67 2.607
213
c ACT027 Acute Pancreatitis 60 2.607
214
P LVR013 Liver Disease 69 2.587
215
MSC157 Muscular Dystrophy, Duchenne Type 79 2.583
216
JPN002 Japanese Encephalitis 61 2.583
217
P OST002 Osteoporosis 76 2.558
218
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 2.558
219
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 2.558
220
BNR002 Bone Resorption Disease 47 2.558
221
P HPT023 Hepatocellular Carcinoma 96 2.558
222
P SLP005 Sleep Disorder 61 2.558
223
VCC001 Vaccinia 47 2.543
224
P LKM002 Leukemia 67 2.534
225
CHR066 Chronic Fatigue Syndrome 60 2.533
226
ALC007 Alcohol Dependence 66 2.531
227
c HPT003 Hepatitis a 63 2.528
228
P ALC033 Alcohol Use Disorder 61 2.511
229
HMN014 Human Immunodeficiency Virus Infectious Disease 54 2.494
230
P CYS018 Cystitis 59 2.470
231
INT007 Intermediate Coronary Syndrome 54 2.449
232
BRN024 Bronchitis 67 2.428
233
P ADL017 Adult T-Cell Leukemia 56 2.403
234
CHR074 Choriocarcinoma 46 2.403
235
P INF032 Infertility 57 2.403
236
OPT003 Opiate Dependence 49 2.386
237
HMC014 Homocysteinemia 52 2.386
238
CRB004 Cerebral Artery Occlusion 45 2.386
239
HDN002 Head Injury 44 2.386
240
P LKM062 Leukemia, Acute Lymphoblastic 69 2.386
241
P BND020 Bone Disease 59 2.376
242
P RST001 Restless Legs Syndrome 52 2.365
243
P CRD119 Cardiac Arrest 67 2.365
244
P SLW003 Slow-Channel Congenital Myasthenic Syndrome 35 2.348
245
FTT001 Fatty Liver Disease 62 2.348
246
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 2.343
247
TXC005 Toxic Shock Syndrome 62 2.343
248
SCH014 Schistosomiasis 56 2.343
249
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 2.320
250
DSS032 Disease by Infectious Agent 55 2.320
251
HMP005 Hemiplegia 54 2.320
252
TBC004 Tobacco Addiction 63 2.299
253
c DLT002 Dilated Cardiomyopathy 78 2.299
254
P SBS003 Substance Abuse 54 2.293
255
c TYP008 Type 1 Diabetes Mellitus 70 2.277
256
ACT098 Acute Erythroid Leukemia 55 2.277
257
END086 End Stage Renal Disease 52 2.260
258
RDC002 Radiculopathy 52 2.260
259
PRS045 Prostatic Hypertrophy 53 2.255
260
MRP001 Morphine Dependence 42 2.247
261
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 2.234
262
HPT004 Hepatic Coma 43 2.234
263
DYS015 Dysentery 50 2.232
264
P BRS047 Breast Cancer 98 2.230
265
PPT005 Peptic Ulcer Disease 58 2.215
266
c PLM164 Pulmonary Hypertension, Primary, 1 76 2.209
267
P PRD008 Periodontitis 64 2.209
268
ADN018 Adenoma 59 2.204
269
RYN005 Raynaud Phenomenon 45 2.204
270
c SML038 Small Cell Cancer of the Lung 69 2.186
271
P GLM040 Glioma Susceptibility 1 71 2.186
272
P MVM001 Movement Disease 61 2.186
273
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 2.186
274
LVR012 Liver Cirrhosis 63 2.186
275
HYP056 Hypoglycemia 65 2.186
276
URM002 Uremia 47 2.173
277
ARG004 Argyria 26 2.163
278
P THR014 Thrombocytopenia 66 2.163
279
DNG003 Dengue Disease 65 2.163
280
c HMN021 Human T-Cell Leukemia Virus Type 1 47 2.163
281
TRG002 Trigeminal Neuralgia 61 2.157
282
c PNS012 Paine Syndrome 60 2.150
283
P ADN016 Adenocarcinoma 63 2.142
284
END057 Endometrial Cancer 72 2.139
285
c ATS007 Autism Spectrum Disorder 72 2.139
286
P MSC003 Muscular Atrophy 52 2.139
287
GLB002 Glioblastoma 67 2.120
288
P SLP006 Sleep Apnea 69 2.115
289
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 2.115
290
ACN002 Acanthosis Nigricans 56 2.111
291
P MLT020 Multiple Sclerosis 79 2.091
292
PLM010 Pulmonary Edema 55 2.091
293
P SCL018 Scoliosis 57 2.079
294
P MLN007 Male Infertility 56 2.079
295
DPH001 Diphtheria 59 2.079
296
P PNC044 Pancreatitis 61 2.079
297
P ART022 Arthritis 71 2.067
298
SNS003 Sensory Peripheral Neuropathy 52 2.067
299
AVN001 Avian Influenza 61 2.047
300
DFC004 Deficiency Anemia 74 2.046
301
P HRP006 Herpes Simplex 65 2.046
302
DRM006 Dermatitis 62 2.046
303
BRN028 Brain Cancer 74 2.045
304
P BLD134 Bladder Cancer 79 2.042
305
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 2.042
306
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 2.042
307
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 2.042
308
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 2.042
309
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 2.042
310
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 2.042
311
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 2.042
312
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 2.042
313
P MDL005 Medulloblastoma 75 2.042
314
CHL067 Cholecystitis 60 2.042
315
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 2.042
316
P PTS002 Ptosis 52 2.042
317
P URT039 Urticaria 58 2.042
318
P SMK004 Smoking As a Quantitative Trait Locus 3 44 2.017
319
CRN030 Coronary Stenosis 50 2.017
320
P NRC002 Narcolepsy 56 2.017
321
ALL006 Allergic Asthma 56 2.017
322
MST020 Mast Cell Activation Syndrome 28 2.017
323
c DNT047 Dentinogenesis Imperfecta Type 2 35 2.017
324
P URN019 Urinary Tract Infection 49 2.012
325
BCT022 Bacterial Infectious Disease 56 2.012
326
GT001 Gout 64 2.012
327
PRS129 Prostatic Hyperplasia, Benign 49 1.991
328
c CHR684 Chronic Kidney Disease 69 1.991
329
PRS021 Prostatic Adenoma 43 1.991
330
c PRM005 Primary Hyperparathyroidism 59 1.984
331
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 1.978
332
P LNG028 Long Qt Syndrome 64 1.966
333
ATN005 Autonomic Dysfunction 46 1.966
334
c LKM061 Leukemia, Acute Myeloid 83 1.965
335
PLG002 Plague 58 1.955
336
P EPS003 Episodic Ataxia 59 1.952
337
c PSR021 Psoriasis 14, Pustular 58 1.943
338
CRD132 Cardiac Conduction Defect 60 1.940
339
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 1.940
340
ATR057 Atrioventricular Block 54 1.940
341
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 1.940
342
MNT002 Mental Depression 57 1.940
343
P THY032 Thyroiditis 57 1.940
344
TND005 Tendinitis 54 1.913
345
c PCH010 Pachyonychia Congenita 3 43 1.913
346
LNG099 Lung Disease 62 1.913
347
P ECL001 Eclampsia 52 1.913
348
MYL069 Myeloma, Multiple 77 1.906
349
P RTN024 Retinoblastoma 73 1.906
350
OST011 Osteomalacia 52 1.906
351
P GLM007 Glomerulonephritis 60 1.904
352
EHR002 Ehrlichiosis 39 1.902
353
TRT001 Teratocarcinoma 42 1.886
354
MTB004 Metabolic Acidosis 48 1.869
355
c BRN108 Branchiootic Syndrome 1 62 1.869
356
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.869
357
P CRD246 Cardiovascular System Disease 56 1.869
358
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.859
359
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 1.859
360
CVD001 Covid-19 57 1.859
361
P FTL001 Fetal Alcohol Syndrome 55 1.859
362
RTN020 Retinal Vascular Disease 46 1.859
363
P MJR001 Major Depressive Disorder 68 1.832
364
P VNS003 Venous Insufficiency 55 1.832
365
P GLL022 Guillain-Barre Syndrome 60 1.832
366
RLP002 Relapsing-Remitting Multiple Sclerosis 56 1.832
367
MLG169 Malignant Astrocytoma 57 1.832
368
FLR002 Filariasis 55 1.832
369
P TMP001 Temporal Lobe Epilepsy 49 1.832
370
CHR178 Chromosomal Triplication 34 1.832
371
CRD223 Cardiac Arrhythmia 63 1.831
372
P PTT006 Pituitary Adenoma 55 1.831
373
P TXP001 Toxoplasmosis 60 1.829
374
ENT011 Enterocolitis 55 1.804
375
CMM005 Common Cold 56 1.804
376
LMY002 Leiomyoma 51 1.792
377
PRT036 Peritonitis 65 1.792
378
ACQ007 Acquired Immunodeficiency Syndrome 59 1.789
379
BRX001 Bruxism 51 1.788
380
c DWL002 Dowling-Degos Disease 1 58 1.775
381
TND004 Tendinopathy 45 1.775
382
TRD006 Tardive Dyskinesia 53 1.775
383
ODN023 Odontochondrodysplasia 67 1.775
384
P OPN001 Open-Angle Glaucoma 55 1.775
385
P RTN018 Retinal Disease 53 1.775
386
P MYC008 Myocarditis 59 1.775
387
ABD010 Abdominal Wall Defect 39 1.775
388
CYN002 Cyanosis, Transient Neonatal 43 1.751
389
OST017 Osteomyelitis 63 1.751
390
P PLY041 Polymyositis 59 1.751
391
PRP016 Paraplegia 52 1.751
392
CNG034 Congestive Heart Failure 69 1.747
393
WST005 West Nile Virus 57 1.744
394
c GLC092 Glaucoma, Primary Open Angle 62 1.717
395
HPT019 Hepatic Encephalopathy 59 1.717
396
P FML187 Familial Hypertension 34 1.717
397
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.710
398
THR024 Thrombosis 56 1.710
399
CRH001 Crohn's Disease 80 1.710
400
P PNC035 Pancreatic Cancer 86 1.701
401
PLR008 Pleurisy 50 1.699
402
c SCL052 Scleroderma, Familial Progressive 61 1.687
404
EMB004 Embryonal Carcinoma 56 1.687
405
P MTR014 Motor Neuron Disease 65 1.687
406
P SYP003 Syphilis 59 1.687
407
THR013 Thoracic Outlet Syndrome 45 1.684
408
ADP001 Adiposis Dolorosa 44 1.668
409
WST003 West Nile Fever 40 1.668
410
P MMP001 Mumps 57 1.667
411
DFF005 Diffuse Large B-Cell Lymphoma 54 1.666
412
KRN002 Kearns-Sayre Syndrome 63 1.666
413
P MYL006 Myeloid Leukemia 61 1.666
414
P DRM010 Dermatomyositis 61 1.666
415
ATN004 Autonomic Neuropathy 42 1.666
416
STR067 Stroke, Ischemic 80 1.657
417
P GST053 Gastric Cancer 83 1.657
418
ILS001 Ileus 50 1.657
419
P INT143 Interstitial Cystitis 60 1.657
420
P ADL010 Adult Respiratory Distress Syndrome 71 1.657
421
SQM006 Squamous Cell Carcinoma 60 1.657
422
LST001 Listeriosis 59 1.652
423
c SPR009 Sporadic Breast Cancer 42 1.632
424
c THY107 Thymoma, Familial 42 1.626
425
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 1.626
426
P HYP750 Hypertriglyceridemia, Familial 62 1.626
427
P RNV001 Renovascular Hypertension 49 1.626
428
P THY023 Thymoma 64 1.626
429
CHR073 Choreatic Disease 54 1.626
430
PRS063 Paresthesia 39 1.626
431
MYL009 Myelodysplastic Syndrome 67 1.621
433
c HYP538 Hypogonadotropic Hypogonadism 17 with or Without Anosmia 25 1.621
434
SPN020 Spondylosis 46 1.621
435
CLN015 Colon Adenocarcinoma 65 1.621
436
ING001 Inguinal Hernia 59 1.621
437
NRM004 Neuroma 49 1.621
438
P MNN013 Meningitis 65 1.621
439
P LNG032 Lung Cancer 98 1.594
441
OST159 Osteogenic Sarcoma 66 1.594
442
MNN043 Meningioma, Familial 79 1.594
443
GLC003 Glucose Intolerance 54 1.594
444
c VRL010 Viral Hepatitis 53 1.594
445
SCR001 Secretory Meningioma 40 1.594
446
LYM002 Lymphoplasmacyte-Rich Meningioma 35 1.594
447
GST045 Gastroenteritis 58 1.594
448
SPN021 Spinal Meningioma 50 1.594
449
DRG003 Drug Dependence 46 1.594
450
CHC001 Chickenpox 57 1.577
451
c EPS035 Episodic Ataxia, Type 2 63 1.574
452
ANR007 Anorexia Nervosa 60 1.574
453
P RTN016 Retinal Degeneration 52 1.574
454
SVR004 Severe Combined Immunodeficiency 72 1.574
455
PRN014 Paronychia 50 1.574
456
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 1.562
457
NRR001 Neuroretinitis 42 1.562
458
RTN023 Retinitis 46 1.562
459
SYN036 Syncope 45 1.562
460
HRT011 Heart Septal Defect 49 1.562
461
HYD002 Hydronephrosis 58 1.562
462
CRD001 Cardiac Tamponade 43 1.562
463
PRP030 Purpura 54 1.562
464
GST023 Gastric Ulcer 52 1.562
465
LYM017 Lyme Disease 62 1.551
466
SXL003 Sexual Disorder 49 1.529
467
PSD012 Pseudoachondroplasia 59 1.529
468
c HYD064 Hydrocephalus, Congenital, 1 51 1.529
469
CRD137 Cardiogenic Shock 56 1.529
470
P PMP001 Pemphigus 55 1.529
471
P NTR004 Neutropenia 63 1.529
472
ALC006 Alcoholic Hepatitis 61 1.529
473
PRT013 Portal Hypertension 59 1.529
474
NRL005 Neurilemmoma 60 1.529
475
ACS001 Acoustic Neuroma 56 1.525
476
P HYP061 Hypertrophic Cardiomyopathy 69 1.525
477
P DYS021 Dysautonomia 38 1.525
478
HMP009 Haemophilus Influenzae 41 1.525
479
P CHR071 Charcot-Marie-Tooth Disease 64 1.496
480
INS024 Insulin-Like Growth Factor I 78 1.496
481
P MYS005 Myositis 56 1.496
482
LMB062 Limb Ischemia 55 1.496
483
P HYP111 Hyperprolinemia 45 1.496
484
P GST044 Gastritis 55 1.496
485
FCL014 Focal Epilepsy 53 1.496
486
RTN001 Retinal Vasculitis 46 1.496
487
P HRT032 Heart Disease 81 1.496
488
EXC002 Exocrine Pancreatic Insufficiency 42 1.496
489
PLM033 Pulmonary Embolism 58 1.496
490
P CRB088 Cerebral Atrophy 33 1.496
491
c MYS068 Myasthenic Syndrome, Congenital, 20, Presynaptic 42 1.485
492
FSC002 Fascioliasis 44 1.473
493
SPN051 Spondylitis 51 1.473
494
INF009 Inflammatory Spondylopathy 30 1.473
495
EPD005 Epidural Abscess 31 1.473
496
PRT029 Parathyroid Adenoma 51 1.473
497
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 1.461
498
PRP080 Peripheral Artery Disease 54 1.461
499
HSH003 Hashimoto Thyroiditis 60 1.461
500
CMP010 Complex Regional Pain Syndrome 60 1.461
501
c ACT068 Acute Cystitis 61 1.461
502
HYP068 Hyperostosis 47 1.461
503
P ART021 Arteriosclerosis 54 1.461
504
HYP014 Hyperuricemia 51 1.461
505
P SCK005 Sickle Cell Disease 56 1.461
506
SDD001 Sudden Infant Death Syndrome 60 1.426
507
P DRM053 Dermatitis, Atopic 65 1.426
508
GST092 Gastroesophageal Reflux 61 1.426
509
CYS001 Cystic Fibrosis 78 1.426
510
P BRG001 Brugada Syndrome 69 1.426
511
MSC007 Muscle Hypertrophy 64 1.426
512
PRT251 Proteinuria, Chronic Benign 57 1.426
513
SCH068 Schwartz-Jampel Syndrome, Type 1 52 1.426
514
GST050 Gastrointestinal System Disease 55 1.426
515
P TRT010 Teratoma 51 1.426
516
LKS001 Leukostasis 41 1.426
517
SPS019 Spastic Paraparesis 38 1.418
518
HYP017 Hypophosphatemia 49 1.418
519
P LYM118 Lymphoma 67 1.418
520
MYL057 Myelopathy, Htlv-1-Associated 38 1.418
521
RTR001 Retrograde Amnesia 41 1.418
522
TRP002 Tropical Spastic Paraparesis 49 1.418
523
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 38 1.418
524
c ALZ063 Alzheimer's Disease 1 31 1.390
525
END062 Endometrial Hyperplasia 48 1.390
526
NNL006 Non-Alcoholic Steatohepatitis 54 1.390
527
P MLN008 Melanoma 76 1.390
528
BRC012 Brucellosis 66 1.390
529
P CNJ013 Conjunctivitis 66 1.390
530
P EYD002 Eye Disease 57 1.390
531
TYP007 Typhoid Fever 64 1.390
532
ORP003 Oropharynx Cancer 55 1.390
533
MYT011 Myotonia 39 1.390
534
c SPR086 Spermatogenic Failure 3 46 1.368
535
P LPR021 Leprosy 3 71 1.360
536
DNG001 Dengue Shock Syndrome 40 1.360
537
HNS001 Hansen's Disease 32 1.360
538
P HYP265 Hypotonia 42 1.360
539
PSR001 Psoriatic Arthritis 62 1.353
540
BRT054 Brittle Bone Disorder 74 1.353
541
OTT002 Otitis Media 71 1.353
542
APH002 Aphasia 56 1.353
543
P FML023 Familial Hemiplegic Migraine 53 1.353
544
c MYS046 Myasthenic Syndrome, Congenital, 1a, Slow-Channel 44 1.353
545
c HYD046 Hydatidiform Mole, Recurrent, 1 59 1.353
546
MLT157 Multiple System Atrophy 1 69 1.353
547
HRW001 Hair Whorl 35 1.353
548
c LRG001 Large Cell Carcinoma 48 1.353
549
P PRS038 Personality Disorder 65 1.353
550
LNG039 Lung Squamous Cell Carcinoma 57 1.353
551
CNN005 Connective Tissue Disease 67 1.353
552
P PLY018 Polycythemia 56 1.353
553
PLC002 Plica Syndrome 35 1.353
554
P GRV001 Graves' Disease 55 1.353
555
c SCN007 Secondary Hyperparathyroidism 51 1.353
556
EXS001 Exostosis 49 1.353
557
NRT004 Neuritis 53 1.353
558
P PLY011 Polycystic Ovary Syndrome 57 1.353
559
PHR003 Pharyngitis 58 1.353
560
P NRF002 Neurofibromatosis 57 1.353
561
EBL001 Ebola Hemorrhagic Fever 56 1.350
562
P OVR082 Overgrowth Syndrome 49 1.315
563
P KLZ004 Kala-Azar 1 41 1.315
564
ACH043 Achondroplasia, Severe, with Developmental Delay and Acanthosis Nigricans 58 1.315
565
P SRC025 Sarcoidosis 1 71 1.315
566
LSH001 Leishmaniasis 64 1.315
567
P MLG056 Malignant Hyperthermia 66 1.315
568
GST010 Gestational Trophoblastic Neoplasm 52 1.315
569
LYM027 Lymphopenia 56 1.315
570
P END046 Endometritis 46 1.315
571
P END044 Endometriosis 62 1.315
572
SPL018 Splenomegaly 49 1.315
573
ALL014 Allergic Encephalomyelitis 34 1.315
574
P PST095 Post-Thrombotic Syndrome 51 1.307
575
BBS001 Babesiosis 49 1.307
576
c HPT016 Hepatitis B 62 1.293
577
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 1.275
578
c ACT134 Acute Liver Failure 59 1.275
579
WTH001 Withdrawal Disorder 48 1.275
580
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.275
581
LPT014 Leptin Deficiency or Dysfunction 78 1.275
582
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.275
583
ACT069 Acute Endometritis 23 1.275
584
GSG001 Gas Gangrene 52 1.275
585
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 1.275
586
P DNG005 Dengue Virus 56 1.275
587
P ATR010 Atrial Heart Septal Defect 58 1.275
588
GST033 Gestational Diabetes 61 1.275
589
P MCR010 Microcephaly 60 1.275
590
P PRN023 Prion Disease 60 1.275
591
SYN007 Synovitis 55 1.275
592
P EPD016 Epidermolysis Bullosa 53 1.275
593
GST037 Gastroparesis 52 1.275
594
IRN002 Iron Metabolism Disease 57 1.275
595
P TRC031 Trichorhinophalangeal Syndrome 38 1.275
596
PTH003 Pathologic Nystagmus 52 1.275
597
P CRN300 Coronary Heart Disease 1 73 1.235
598
GLL008 Gilles De La Tourette Syndrome 65 1.235
599
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 1.235
600
c ART101 Aortic Valve Disease 2 66 1.235
601
DBT081 Diabetic Encephalopathy 36 1.235
602
c ACT075 Acute Myocardial Infarction 56 1.235
603
EXP004 Exophthalmos 51 1.235
604
ULC004 Ulcerative Colitis 74 1.235
605
PRG001 Progressive Muscular Atrophy 41 1.235
606
P SPN046 Spinal Muscular Atrophy 63 1.235
607
CHL123 Chlamydia 58 1.235
608
CHL068 Cholestasis 61 1.235
609
CGH002 Cough Headache 16 1.235
610
SPN185 Spinal Cord Infarction 28 1.232
611
LYM009 Lymphocytic Choriomeningitis 46 1.232
612
P MXL015 Maxillary Sinusitis 38 1.232
613
AMN014 Aminopterin Syndrome Sine Aminopterin 32 1.229
614
c SPN225 Spondyloarthropathy 1 70 1.229
615
BTT016 Batten-Turner Congenital Myopathy 53 1.229
616
P ALP008 Alopecia 54 1.229
617
THR016 Thrombophlebitis 50 1.229
618
FCL012 Facial Paralysis 49 1.229
619
PLM031 Poliomyelitis 63 1.229
620
P FRG001 Fragile X Syndrome 70 1.193
621
HMR023 Hemorrhagic Cystitis 43 1.193
622
HYP003 Hypermethioninemia 51 1.193
623
P PLY014 Polycystic Kidney Disease 69 1.193
624
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 1.193
625
IGR001 Ige Responsiveness, Atopic 59 1.193
626
SPN209 Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations 66 1.193
627
PMP006 Pemphigus Vulgaris, Familial 58 1.193
628
P DDN001 Duodenal Ulcer 53 1.193
629
P NPH012 Nephrotic Syndrome 60 1.193
630
P ACH003 Achromatopsia 62 1.193
631
SGN002 Signet Ring Cell Adenocarcinoma 46 1.193
632
GLC036 Glucagonoma 46 1.193
633
TNS014 Tenosynovitis 46 1.193
634
PST053 Postherpetic Neuralgia 40 1.193
635
MMB001 Membranoproliferative Glomerulonephritis 56 1.191
636
C3G002 C3 Glomerulopathy 46 1.191
637
P TRN020 Turner Syndrome 67 1.161
638
c MYS074 Myasthenic Syndrome, Congenital, 12 45 1.159
639
ALK013 Alkaptonuria 59 1.154
640
OST160 Osteoid Osteoma 37 1.154
641
c SVR005 Severe Pre-Eclampsia 50 1.154
642
MYL080 Myalgic Encephalomyelitis/chronic Fatigue Syndrome 29 1.154
643
c GLL024 Gallbladder Disease 1 52 1.150
644
ALL003 Allergic Rhinitis 67 1.150
645
SNL009 Senile Plaque Formation 29 1.150
646
P CRC039 Coarctation of Aorta 46 1.150
647
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 1.150
648
P HMC002 Homocystinuria 53 1.150
649
P ART023 Arthropathy 61 1.150
650
P CTR002 Cataract 60 1.150
651
CHL045 Choline Deficiency Disease 39 1.150
652
P LNG064 Lung Cancer Susceptibility 3 70 1.150
653
TNS005 Tonsillitis 57 1.150
654
MNN009 Meningoencephalitis 48 1.150
655
MCR013 Microphthalmia 60 1.150
656
P INT068 Intestinal Disease 53 1.150
657
P PNM007 Pneumonia 67 1.150
658
BNN003 Bone Inflammation Disease 48 1.150
659
GNR004 Generalized Anxiety Disorder 55 1.150
660
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 1.150
661
TLR001 Tularemia 56 1.150
662
HRP004 Herpes Zoster 61 1.150
663
MYC005 Myocardial Stunning 46 1.150
664
ANR040 Aneurysm 61 1.150
665
MLT075 Multifocal Motor Neuropathy 45 1.150
666
HDC005 Headache Associated with Sexual Activity 17 1.147
667
HYP781 Hypoascorbemia 52 1.147
668
MYP071 Myopathy Due to Myoadenylate Deaminase Deficiency 43 1.147
669
P PLM036 Pulmonary Fibrosis 66 1.147
670
P SJG008 Sjogren Syndrome 61 1.105
671
CRT072 Creutzfeldt-Jakob Disease 68 1.105
672
P CLC063 Celiac Disease 1 66 1.105
673
ELL001 Ellis-Van Creveld Syndrome 62 1.105
674
P GLC113 Galactosemia I 66 1.105
675
OCL052 Ocular Dominance 40 1.105
676
PLM196 Pulmonary Adenocarcinoma in Situ 36 1.105
677
THY029 Thyroid Carcinoma 51 1.105
678
CTN007 Cutaneous Leishmaniasis 62 1.105
679
LRN003 Learning Disability 49 1.105
680
P ACN011 Acne 57 1.105
681
HYP005 Hypokalemia 55 1.105
682
OST003 Osteonecrosis 61 1.105
683
DNG002 Dengue Hemorrhagic Fever 60 1.105
684
FRZ001 Frozen Shoulder 55 1.105
685
MCS002 Mucositis 56 1.105
686
PLC009 Placenta Praevia 38 1.105
687
STL001 St. Louis Encephalitis 38 1.105
688
P END033 Endocarditis 58 1.105
689
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 50 1.105
690
c FML021 Familial Hypercholesterolemia 72 1.105
691
CRT033 Corticobasal Degeneration 47 1.105
692
STM006 Stomach Disease 47 1.074
693
PRS120 Persistent Idiopathic Facial Pain 27 1.069
694
PFF001 Pfeiffer Syndrome 77 1.069
695
VTM002 Vitamin B12 Deficiency 48 1.069
696
OPP004 Oppositional Defiant Disorder 49 1.069
697
P MCR129 Microvascular Complications of Diabetes 1 68 1.069
698
FDL002 Food Allergy 47 1.069
699
c SCN006 Secondary Syphilis 36 1.069
700
c MCR112 Microvascular Complications of Diabetes 2 42 1.069
701
MLN003 Melancholia 41 1.069
702
P PYL005 Pyelonephritis 57 1.069
703
DBT004 Diabetic Polyneuropathy 50 1.069
704
CND002 Conduct Disorder 51 1.069
705
OCH001 Ochronosis 40 1.069
706
NCR015 Necrotizing Autoimmune Myopathy 27 1.069
707
c RNG024 Ring Chromosome 8 28 1.069
708
SPN392 Spondylosis, Cervical 30 1.058
709
c DPH024 Diaphragmatic Hernia, Congenital 64 1.058
710
ESP021 Esophageal Cancer 83 1.058
711
c NRF024 Neurofibromatosis, Type I 72 1.058
712
CHR431 Chronic Venous Insufficiency 48 1.058
713
P LPS004 Lupus Erythematosus 61 1.058
714
P HYP077 Hypertrichosis 46 1.058
715
c FML191 Familial Long Qt Syndrome 55 1.058
716
P OPT006 Optic Nerve Disease 58 1.058
717
MYF002 Myofascial Pain Syndrome 46 1.058
718
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.058
719
CHL147 Chlamydia Pneumonia 47 1.058
720
GTR002 Goiter 53 1.058
721
P ANG015 Angioedema 56 1.058
722
BRS064 Bursitis 51 1.058
723
HMP001 Hemopericardium 47 1.058
724
P PRC012 Pericardial Effusion 50 1.058
725
ALC005 Alcoholic Pancreatitis 38 1.058
726
MNN017 Mononeuropathy 41 1.058
727
LPT001 Leptospirosis 66 1.058
728
NRN004 Neuroendocrine Tumor 59 1.058
729
WLL004 Wallerian Degeneration 38 1.058
730
BNN005 Bunion 31 1.058
731
HMN001 Human Monocytic Ehrlichiosis 30 1.045
732
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 1.045
733
P LCT002 Lactose Intolerance 52 1.045
734
P RBL001 Rubella 58 1.045
735
CCC001 Coccidioidomycosis 58 1.045
736
SPT005 Spotted Fever 49 1.045
737
RHM001 Rheumatic Fever 59 1.045
738
HRN003 Heroin Dependence 44 1.045
739
LVT001 Levator Syndrome 19 1.045
740
PRF003 Piriformis Syndrome 25 1.045
741
CFH006 Cfhr5 Deficiency 36 1.032
742
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 1.008
743
INT146 Intervertebral Disc Disease 63 1.008
744
c SYS001 Systemic Lupus Erythematosus 87 1.008
745
FDB001 Foodborne Botulism 55 1.008
746
INF034 Infective Endocarditis 54 1.008
747
P CRP001 Carpal Tunnel Syndrome 66 1.008
748
P MPL001 Maple Syrup Urine Disease 70 1.008
749
P SPP010 Suppressor of Tumorigenicity 3 51 1.008
750
ADN011 Adenoid Cystic Carcinoma 68 1.008
751
P RHB003 Rhabdomyosarcoma 66 1.008
752
P RRH023 Rare Hereditary Hemochromatosis 54 1.008
753
P FBR017 Fibrosarcoma 56 1.008
754
TRY001 Trypanosomiasis 50 1.008
755
HMS001 Hemosiderosis 48 1.008
756
VRC001 Varicocele 48 1.008
757
PNC001 Pancytopenia 53 1.008
758
P BNG032 Benign Mesothelioma 53 1.008
759
SMT001 Somatization Disorder 50 1.008
760
P CMP008 Compartment Syndrome 50 1.008
761
ORL011 Oral Cancer 60 1.008
762
CLD011 Cold Urticaria 34 1.008
763
PRX097 Paroxysmal Dystonia 32 0.967
764
PLR007 Pleural Empyema 51 0.967
765
CNT047 Contact Dermatitis 57 0.967
766
LMR001 Lemierre's Syndrome 39 0.967
767
FTD001 Foot Drop 35 0.967
768
MYC015 Mycobacterium Fortuitum 28 0.967
769
c GLC111 Galactosemia Ii 50 0.957
770
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 50 0.957
771
MDR006 Moderate and Severe Traumatic Brain Injury 27 0.957
772
P THL005 Thalassemia 56 0.957
773
SCR039 Scorpion Envenomation 41 0.957
774
P WSK001 Wiskott-Aldrich Syndrome 72 0.957
775
ONC007 Oncocytoma 50 0.957
776
P MYC084 Mycobacterium Tuberculosis 1 68 0.957
777
OVR029 Ovarian Hyperstimulation Syndrome 63 0.957
778
P CLR023 Colorectal Cancer 100 0.957
779
EPD015 Epidemic Typhus 44 0.957
780
FTL006 Fetal Alcohol Spectrum Disorder 43 0.957
781
c MCR130 Microvascular Complications of Diabetes 6 41 0.957
782
KRT019 Keratitis, Hereditary 66 0.957
783
SCK003 Sickle Cell Anemia 74 0.957
784
c MCR120 Microvascular Complications of Diabetes 7 47 0.957
785
BLC001 Blue Cone Monochromacy 45 0.957
786
HMC041 Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity 48 0.957
788
MDD018 Middle East Respiratory Syndrome 44 0.957
789
ELP001 Elephantiasis 44 0.957
790
PRP007 Priapism 47 0.957
791
CLF001 Cleft Lip 53 0.957
792
PRS034 Parasitic Helminthiasis Infectious Disease 51 0.957
793
AMB001 Amebiasis 57 0.957
794
P HMR005 Hemorrhoid 49 0.957
795
INT002 Intermittent Claudication 61 0.957
796
P OLV001 Olivopontocerebellar Atrophy 51 0.957
797
AVD001 Avoidant Personality Disorder 49 0.957
798
P PNC025 Panic Disorder 52 0.957
799
APP008 Appendicitis 62 0.957
800
MLG079 Malignant Pleural Mesothelioma 42 0.957
801
c MCR113 Microvascular Complications of Diabetes 3 52 0.957
802
c MCR133 Microvascular Complications of Diabetes 4 41 0.957
803
P MGR001 Migraine Without Aura 49 0.957
804
TLN003 Telangiectasis 51 0.957
805
BLR008 Bilirubin Metabolic Disorder 57 0.957
806
CRD003 Cardiac Sarcoidosis 44 0.957
807
ALC009 Alcoholic Liver Cirrhosis 54 0.957
808
P NNT006 Neonatal Myasthenia Gravis 27 0.957
809
PPL002 Papillary Carcinoma 46 0.957
810
P RNL015 Renal Hypertension 45 0.957
811
ANT019 Anterograde Amnesia 38 0.957
812
P OVR046 Ovarian Cyst 46 0.957
813
DMY004 Demyelinating Disease 50 0.957
814
P HYP050 Hyperinsulinemic Hypoglycemia 57 0.957
815
P MYT002 Myotonic Dystrophy 51 0.957
816
FNT004 Fainting 29 0.957
817
P CLS010 Cluster Headache 42 0.957
818
TRC088 Trochleitis 12 0.913
819
HMN002 Human Granulocytic Anaplasmosis 31 0.913
820
P MYF003 Myofibrillar Myopathy 49 0.913
821
c MYS075 Myasthenic Syndrome, Congenital, 13 39 0.913
822
P PLY017 Polyarteritis Nodosa 60 0.913
823
MNK002 Monkeypox 41 0.913
824
c SBC007 Subacute Thyroiditis 43 0.913
825
HNT002 Hantavirus Pulmonary Syndrome 55 0.913
826
GRW007 Growth Hormone Deficiency 46 0.902
827
CNG506 Congenital Amyoplasia 27 0.902
828
BNG077 Benign Idiopathic Neonatal Seizures 23 0.902
829
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.902
830
ART002 Arts Syndrome 66 0.902
831
VLV047 Volvulus of Midgut 52 0.902
832
c SCH082 Schizophrenia 5 23 0.902
833
RNL065 Renal Cell Carcinoma, Papillary, 1 79 0.902
834
P STR092 Striatal Degeneration, Autosomal Dominant 2 47 0.902
835
P MYS047 Myasthenic Syndrome, Congenital, 1b, Fast-Channel 37 0.902
836
c ALZ058 Alzheimer Disease 11 28 0.902
837
RYN001 Raynaud Disease 50 0.902
838
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.902
839
PRM329 Premature Aging 36 0.902
840
ILL008 Ileal Neuroendocrine Tumor 20 0.902
841
BRN004 Brain Edema 54 0.902
842
MNG007 Manganese Poisoning 28 0.902
843
P VNT002 Ventricular Septal Defect 58 0.902
844
HRT012 Heart Valve Disease 53 0.902
845
THY123 Thyroid Gland Follicular Carcinoma 55 0.902
846
P RNL017 Renal Oncocytoma 54 0.902
847
c VRL007 Viral Encephalitis 50 0.902
848
CHL004 Cholelithiasis 49 0.902
849
PCD001 Pica Disease 38 0.902
850
ACR007 Acromegaly 70 0.902
851
KRT009 Keratosis 53 0.902
852
P MTH007 Methemoglobinemia 46 0.902
853
THY020 Thyroid Hyalinizing Trabecular Adenoma 20 0.902
854
PRM020 Premenstrual Tension 39 0.902
855
CCN002 Cocaine Abuse 49 0.902
856
SPT004 Septic Arthritis 58 0.902
857
CYS002 Cystic Lymphangioma 45 0.902
858
P LRY044 Larynx Cancer 54 0.902
859
CRT016 Carotid Artery Disease 52 0.902
860
P PRP029 Porphyria 60 0.902
861
LNG015 Lingual-Facial-Buccal Dyskinesia 47 0.902
862
c JVN010 Juvenile Rheumatoid Arthritis 66 0.902
863
GRN017 Granulocytopenia 42 0.902
864
FSC004 Fasciitis 49 0.902
865
CCN001 Cocaine Dependence 48 0.902
866
ORL012 Oral Leukoplakia 36 0.902
868
LKP003 Leukoplakia 39 0.902
869
CHR176 Chromophil Renal Cell Carcinoma 23 0.902
870
P ENC008 Encephalocele 46 0.902
871
HVY002 Heavy Metal Poisoning 22 0.902
872
PRN019 Perinatal Necrotizing Enterocolitis 60 0.902
873
c MYS067 Myasthenic Syndrome, Congenital, 22 35 0.890
874
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.870
875
SPN050 Spinocerebellar Degeneration 39 0.844
876
P OTT001 Otitis Externa 42 0.844
877
SPS057 Spasticity 42 0.844
878
P RTT002 Rett Syndrome 79 0.844
879
c MYS055 Myasthenic Syndrome, Congenital, 6, Presynaptic 47 0.844
880
DSC013 Discrimination, Two-Point, Reduction in 21 0.844
881
SYR010 Syringomyelia, Noncommunicating Isolated 36 0.844
882
P PRV006 Pervasive Developmental Disorder 52 0.844
883
ART074 Aortic Dissection 53 0.844
884
c MGR030 Migraine, Familial Hemiplegic, 2 49 0.844
885
c SPN309 Spinocerebellar Ataxia 6 58 0.844
886
TMT002 Temtamy Preaxial Brachydactyly Syndrome 54 0.844
887
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.844
888
c ALZ012 Alzheimer Disease 12 24 0.844
889
c DYS191 Dystonia 1, Torsion, Autosomal Dominant 47 0.844
890
NTR005 Nutritional Deficiency Disease 61 0.844
891
P PRD021 Periodic Paralysis 41 0.844
892
WHP002 Whiplash 36 0.844
893
P OLG002 Oligodendroglioma 66 0.844
894
P BRS044 Breast Adenocarcinoma 58 0.844
895
CLL003 Cellulitis 53 0.844
896
PPL021 Papilledema 49 0.844
897
END040 Endogenous Depression 55 0.844
898
GST040 Gastric Adenocarcinoma 67 0.844
899
SCB001 Scabies 50 0.844
900
MYL001 Myelitis 50 0.844
901
INT060 Intestinal Atresia 41 0.844
902
MLL002 Miller Fisher Syndrome 40 0.844
903
DNT012 Dental Caries 53 0.844
904
CRV040 Cervix Carcinoma 50 0.844
905
SCR008 Scrub Typhus 57 0.844
906
PYL006 Pyloric Stenosis 48 0.844
907
ACL001 Acalculous Cholecystitis 38 0.844
908
BRN038 Bronchial Disease 51 0.844
909
IRN001 Iron Deficiency Anemia 58 0.844
910
HRM003 Hormone Producing Pituitary Cancer 33 0.844
911
P TCD001 Tic Disorder 49 0.844
912
P SYR001 Syringomyelia 47 0.844
913
BRN002 Bronchiolitis 57 0.844
914
PLS007 Plasmodium Falciparum Malaria 52 0.844
915
QDR001 Quadriplegia 50 0.844
916
HYP080 Hypogonadism 50 0.844
917
TRC023 Trichinosis 53 0.844
918
HRP009 Herpes Simplex Encephalitis 58 0.844
919
P MRC003 Mercury Poisoning 49 0.844
920
FBR019 Fibromatosis 42 0.844
921
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.842
922
P HMN038 Human Coronavirus Sensitivity 30 0.842
923
ADL002 Adult Syndrome 70 0.842
924
P ANR048 Aniridia 1 64 0.842
925
VRL011 Viral Infectious Disease 61 0.842
926
INH001 Inhalation Anthrax 42 0.841
927
PHL003 Phlebotomus Fever 33 0.841
928
SRT004 Serotonin Syndrome 54 0.835
929
P FCS012 Facioscapulohumeral Muscular Dystrophy 1 68 0.835
930
NPH113 Nephroma 37 0.835
931
c HYP532 Hypogonadotropic Hypogonadism 18 with or Without Anosmia 27 0.835
932
PRM013 Premature Menopause 58 0.835
933
ERY004 Erysipelas 47 0.835
934
PNF002 Painful Legs and Moving Toes Syndrome 14 0.835
935
CLR108 Colorectal Adenoma 64 0.789
936
PYM001 Pyomyositis 42 0.781
937
P RRT020 Rare Tumor 39 0.781
938
ADN027 Adenomyosis 57 0.781
939
c PNC108 Pancreatitis, Hereditary 69 0.781
940
P OVR042 Ovarian Cancer 88 0.781
941
ATS010 Autosomal Recessive Disease 42 0.781
942
BRR014 Barrett Esophagus 66 0.781
943
NRN005 Neuronal Ceroid-Lipofuscinoses 61 0.781
944
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 60 0.781
945
MYL020 Myelomeningocele 51 0.781
946
P SML001 Small Cell Carcinoma 52 0.781
947
P CHN012 Chondrosarcoma 57 0.781
948
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 0.781
949
c MYS059 Myasthenic Syndrome, Congenital, 4a, Slow-Channel 31 0.781
950
RFL001 Reflex Sympathetic Dystrophy 51 0.781
951
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.781
952
PRP083 Porphyria, Acute Intermittent 65 0.781
953
CHR619 Chromosome 2q35 Duplication Syndrome 64 0.781
954
DNT005 Dentatorubral-Pallidoluysian Atrophy 60 0.781
955
NVS017 Nevus, Epidermal 66 0.781
956
APN008 Apnea, Obstructive Sleep 67 0.781
957
c MYS060 Myasthenic Syndrome, Congenital, 4b, Fast-Channel 26 0.781
958
P MYP006 Myopia 56 0.781
959
P STR001 Striatonigral Degeneration 37 0.781
960
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.781
961
P ART018