Search results for Ketamine

1254 hits were found for Ketamine

# Family MCID Name MIFTS Score
1
PNG002 Pain Agnosia 51 23.237
2
DPR016 Depression 65 22.754
3
MNT002 Mental Depression 56 22.611
4
KTM001 Ketamine-Induced Biliary Dilatation 8 21.202
5
P MJR001 Major Depressive Disorder 68 18.809
6
P CHR345 Chronic Pain 50 14.498
7
END040 Endogenous Depression 54 11.638
8
P SCH015 Schizophrenia 74 10.137
9
NRT001 Neurotic Disorder 56 9.931
10
c MJR024 Major Affective Disorder 9 40 9.862
11
c MJR022 Major Affective Disorder 8 37 9.862
12
P BPL003 Bipolar Disorder 56 9.862
13
c PNS012 Paine Syndrome 60 9.794
14
SBC016 Subacute Delirium 42 9.569
15
PST028 Post-Traumatic Stress Disorder 59 9.420
16
c EPS039 Episodic Pain Syndrome, Familial, 1 42 8.859
17
MDD011 Mood Disorder 62 8.364
18
P CYS018 Cystitis 59 7.852
19
ANX010 Anxiety 70 7.681
20
CMP010 Complex Regional Pain Syndrome 59 7.613
21
ACT084 Acute Stress Disorder 53 7.456
22
STT001 Status Epilepticus 58 7.380
23
48X005 48,xyyy 39 7.258
24
AMN003 Amnestic Disorder 54 6.617
25
P SBS003 Substance Abuse 54 5.877
26
P SZR006 Seizure Disorder 69 5.776
27
OBS002 Obsessive-Compulsive Disorder 68 5.632
28
ALC007 Alcohol Dependence 65 5.590
29
P SCK005 Sickle Cell Disease 56 5.346
30
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 5.252
31
P ALC033 Alcohol Use Disorder 67 5.142
32
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 5.094
33
PSY004 Psychotic Disorder 66 5.082
34
P HDC001 Headache 56 5.056
35
TXC005 Toxic Shock Syndrome 62 5.019
36
P RSP003 Respiratory Failure 74 4.952
37
P MJR007 Major Affective Disorder 1 42 4.709
38
P INT143 Interstitial Cystitis 59 4.664
39
TRM010 Traumatic Brain Injury 50 4.649
40
P CRD119 Cardiac Arrest 68 4.584
41
BRN071 Brain Injury 50 4.490
42
P PRS038 Personality Disorder 65 4.414
43
STT002 Status Asthmaticus 49 4.394
44
RHB024 Rhabdomyosarcoma 2 65 4.354
45
P SCL018 Scoliosis 57 4.350
46
P ANR048 Aniridia 1 66 4.347
47
PTH003 Pathologic Nystagmus 52 4.308
48
c MGR028 Migraine with or Without Aura 1 64 4.267
49
ING001 Inguinal Hernia 59 4.254
50
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 4.185
51
MCS002 Mucositis 55 4.165
52
P SLP006 Sleep Apnea 69 3.984
53
P STR020 Strabismus 56 3.919
54
MCH006 Mechanical Strabismus 40 3.919
55
FBR047 Fibromyalgia 58 3.827
56
PST021 Postpartum Depression 50 3.791
57
P TRN020 Turner Syndrome 67 3.781
58
c MJR008 Major Affective Disorder 2 34 3.773
59
c MJR006 Major Affective Disorder 5 32 3.773
60
c MJR003 Major Affective Disorder 6 32 3.773
61
c MJR004 Major Affective Disorder 4 28 3.773
62
c MJR023 Major Affective Disorder 7 33 3.773
63
INT075 Intracranial Hypertension 52 3.741
64
CYT002 Cytokine Deficiency 43 3.607
65
AGN016 Aging 54 3.544
66
P CTR002 Cataract 59 3.535
67
OCL069 Ocular Motor Apraxia 57 3.500
68
IDP070 Idiopathic Scoliosis 41 3.485
69
DSS008 Disease of Mental Health 74 3.436
70
RFL001 Reflex Sympathetic Dystrophy 51 3.404
71
ALG001 Algoneurodystrophy 37 3.404
72
HYP266 Hypoxia 56 3.396
73
ADL002 Adult Syndrome 69 3.322
74
OPT003 Opiate Dependence 49 3.307
75
OPD006 Opioid Addiction 48 3.253
76
HDN002 Head Injury 44 3.203
77
PST053 Postherpetic Neuralgia 40 3.180
78
P BRS047 Breast Cancer 97 3.176
79
P HRT032 Heart Disease 84 3.173
80
BCK006 Back Pain 43 3.154
81
CNS004 Constipation 56 3.145
82
P CLR023 Colorectal Cancer 100 3.132
83
P TRM003 Tremor 50 3.080
84
c ATS007 Autism Spectrum Disorder 72 3.073
85
ANT039 Antisynthetase Syndrome 55 3.053
86
OPD001 Opioid Abuse 44 3.041
87
P NRP001 Neuropathy 59 3.039
88
ILS001 Ileus 49 3.038
89
CHL079 Children's Interstitial Lung Disease 26 2.950
90
HYD002 Hydronephrosis 58 2.940
91
P PRP019 Peripheral Nervous System Disease 57 2.925
92
SCK003 Sickle Cell Anemia 74 2.897
93
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 2.889
94
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 2.889
95
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 2.889
96
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 2.889
97
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 2.889
98
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 2.889
99
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 2.889
100
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 2.889
101
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 2.889
102
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 2.889
103
P ADL010 Adult Respiratory Distress Syndrome 71 2.873
104
P PLM037 Pulmonary Hypertension 69 2.865
105
AND005 Androgen Insensitivity Syndrome, Mild 21 2.855
106
STR067 Stroke, Ischemic 79 2.853
107
SPN186 Spinal Cord Injury 61 2.833
108
PRT036 Peritonitis 65 2.813
109
P EPL164 Epilepsy 70 2.810
110
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 2.779
111
P ATS364 Autism 72 2.757
112
c HYP595 Hypertension, Essential 84 2.756
113
DFC004 Deficiency Anemia 74 2.751
114
WTH001 Withdrawal Disorder 47 2.700
115
SPR126 Superior Semicircular Canal Dehiscence 41 2.655
116
OBS003 Obsessive-Compulsive Personality Disorder 43 2.655
117
c HMG029 Hemoglobin Se Disease 41 2.655
118
HRT011 Heart Septal Defect 49 2.644
119
CCN001 Cocaine Dependence 48 2.608
120
47X002 47,xyy 48 2.594
121
MTB004 Metabolic Acidosis 48 2.572
122
ALL029 Allergic Disease 61 2.534
123
c ACT071 Acute Kidney Failure 60 2.533
124
ANR007 Anorexia Nervosa 59 2.532
125
CVD001 Covid-19 58 2.519
126
DPR002 Depersonalization Disorder 41 2.490
127
P EXN002 Exanthem 58 2.468
128
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 2.435
129
OST012 Osteoarthritis 77 2.409
130
P CLS010 Cluster Headache 42 2.380
131
LPT014 Leptin Deficiency or Dysfunction 77 2.370
132
CRB004 Cerebral Artery Occlusion 46 2.357
133
P PNC044 Pancreatitis 61 2.344
134
CRB039 Cerebrovascular Disease 65 2.344
135
ISC004 Ischemia 61 2.323
136
SCL003 Social Phobia 48 2.321
137
P VNT002 Ventricular Septal Defect 58 2.321
138
GNR004 Generalized Anxiety Disorder 55 2.321
139
DBT010 Diabetic Neuropathy 54 2.316
140
P CHL066 Cholangitis 51 2.311
141
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 2.306
142
P RTT002 Rett Syndrome 79 2.261
143
c ACT249 Acute Asthma 40 2.261
144
P AST005 Asthma 76 2.251
145
P AGN002 Agnosia 53 2.221
146
PHR003 Pharyngitis 57 2.210
147
P MYC033 Myoclonus 46 2.187
148
VRS002 Virus-Associated Trichodysplasia Spinulosa 30 2.173
149
P NRB001 Neuroblastoma 66 2.171
150
P SLP005 Sleep Disorder 62 2.168
151
P VSC007 Vascular Disease 62 2.163
152
CCN002 Cocaine Abuse 49 2.159
153
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 2.150
154
ANT019 Anterograde Amnesia 38 2.148
155
SPN027 Spinal Stenosis 59 2.146
156
PLM010 Pulmonary Edema 54 2.111
157
P MLT020 Multiple Sclerosis 79 2.107
158
ANR040 Aneurysm 60 2.084
159
c MCL013 Mucolipidosis Iv 64 2.072
160
VSL002 Visual Epilepsy 39 2.072
161
APN008 Apnea, Obstructive Sleep 66 2.058
162
ATX019 Ataxia with Vitamin E Deficiency 44 2.054
163
ADR040 Adrenal Gland Pheochromocytoma 45 2.043
164
P PHC003 Pheochromocytoma 70 2.043
165
HYP066 Hyperglycemia 60 2.043
166
SXL003 Sexual Disorder 49 2.022
167
ANX004 Anoxia 40 2.007
168
ART016 Aortic Aneurysm 69 1.996
169
HYP056 Hypoglycemia 65 1.991
170
P MLG056 Malignant Hyperthermia 65 1.988
171
CRB009 Cerebritis 43 1.978
172
PLM129 Pulmonary Disease, Chronic Obstructive 74 1.961
173
P HMR005 Hemorrhoid 49 1.951
174
P BCL017 B-Cell Lymphoma 57 1.942
175
P MSC005 Muscular Dystrophy 66 1.942
176
MSC157 Muscular Dystrophy, Duchenne Type 79 1.897
177
c GLL024 Gallbladder Disease 1 53 1.892
178
P LRY019 Laryngitis 53 1.891
179
P CNJ013 Conjunctivitis 66 1.881
180
P ADN016 Adenocarcinoma 63 1.879
181
P FNG006 Feingold Syndrome 1 61 1.870
182
ENT001 Enterocele 42 1.870
183
CLF001 Cleft Lip 54 1.869
184
ART140 Arteries, Anomalies of 52 1.841
185
LPP008 Lipoprotein Quantitative Trait Locus 65 1.841
186
AVD001 Avoidant Personality Disorder 49 1.830
187
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 1.825
188
P ART022 Arthritis 70 1.822
189
TTN003 Tetanus 64 1.799
190
c FNC043 Fanconi Anemia, Complementation Group E 62 1.795
191
SCH003 Schizophreniform Disorder 54 1.795
192
CHL067 Cholecystitis 59 1.790
193
RSP019 Respiratory Distress Syndrome in Premature Infants 52 1.785
194
P BLD124 Bleeding Disorder, Platelet-Type, 11 68 1.785
195
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 49 1.785
196
P LRS001 Larsen Syndrome 61 1.785
197
ACT011 Acute Contagious Conjunctivitis 42 1.785
198
NWB001 Newborn Respiratory Distress Syndrome 56 1.785
199
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 1.785
200
RSP007 Respiratory Distress Syndrome, Infant 40 1.785
201
DCB001 Decubitus Ulcer 61 1.768
202
c ACT027 Acute Pancreatitis 60 1.761
203
c EXD008 Exudative Vitreoretinopathy 1 71 1.756
204
PLY068 Polysubstance Abuse 41 1.755
205
HRT012 Heart Valve Disease 53 1.745
206
c CRN243 Carney Complex, Type 1 53 1.743
207
P RTN018 Retinal Disease 53 1.731
208
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 1.729
209
CHR682 Chronic Bilirubin Encephalopathy 37 1.725
210
c ART067 Aortic Aneurysm, Familial Thoracic 1 61 1.712
211
AYM001 Ayme-Gripp Syndrome 57 1.688
212
P LNG032 Lung Cancer 98 1.688
213
LPT006 Leptin Receptor Deficiency 50 1.688
214
MLD017 Mal De Debarquement Syndrome 33 1.688
215
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.678
216
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 1.678
217
P ATR010 Atrial Heart Septal Defect 58 1.664
218
RDC002 Radiculopathy 51 1.663
219
EPT021 Epithelial Recurrent Erosion Dystrophy 46 1.657
220
SMT001 Somatization Disorder 50 1.657
221
SQM013 Squamous Cell Carcinoma, Head and Neck 75 1.657
222
TTH006 Tooth Disease 51 1.654
223
SYN007 Synovitis 54 1.631
224
PLC002 Plica Syndrome 35 1.631
225
PNM008 Pneumothorax 54 1.582
226
LNG099 Lung Disease 62 1.581
227
LYM019 Lymphosarcoma 46 1.576
228
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.574
229
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 1.574
230
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 52 1.574
231
CTS005 Catastrophic Antiphospholipid Syndrome 43 1.573
232
CRY008 Cryopyrin-Associated Periodic Syndrome 48 1.573
233
DRG003 Drug Dependence 46 1.570
234
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 39 1.560
235
P CNR004 Cone-Rod Dystrophy 2 75 1.560
236
P PRV006 Pervasive Developmental Disorder 52 1.560
237
P NRV007 Nervous System Disease 66 1.560
238
P GST044 Gastritis 55 1.559
239
MYF002 Myofascial Pain Syndrome 46 1.541
240
CYN002 Cyanosis, Transient Neonatal 43 1.534
241
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 1.533
242
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.507
243
P DBT005 Diabetes Insipidus 54 1.507
244
ARG004 Argyria 26 1.497
245
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 46 1.493
246
DNT012 Dental Caries 53 1.491
247
P LVR013 Liver Disease 68 1.488
248
c HPT003 Hepatitis a 63 1.487
249
PRP007 Priapism 46 1.478
250
P TTR001 Tetralogy of Fallot 69 1.459
251
MNN017 Mononeuropathy 41 1.449
252
PRS047 Prostatitis 58 1.446
253
MYL069 Myeloma, Multiple 77 1.445
254
BHR001 Behr Syndrome 50 1.445
255
CMR002 Coumarin Resistance 60 1.445
256
DSM003 Desmoid Disease, Hereditary 48 1.445
257
OST062 Osteoarthritis with Mild Chondrodysplasia 47 1.445
258
BCT021 Bacterial Sepsis 43 1.436
259
P HPT021 Hepatitis 68 1.431
260
SPN019 Spondylolisthesis 52 1.429
261
CLF004 Cleft Lip/palate 57 1.429
262
URN010 Urinary Tract Obstruction 55 1.428
263
P EPD016 Epidermolysis Bullosa 53 1.417
264
P TMP001 Temporal Lobe Epilepsy 49 1.410
265
TBC004 Tobacco Addiction 63 1.410
266
CNG034 Congestive Heart Failure 69 1.410
267
P URN019 Urinary Tract Infection 49 1.401
268
P PRP029 Porphyria 60 1.397
269
CRB037 Cerebral Palsy 67 1.395
270
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 38 1.394
271
c HYP724 Hyperlipoproteinemia, Type Iii 66 1.394
272
P CRN300 Coronary Heart Disease 1 73 1.394
273
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 1.391
274
TXC002 Toxic Encephalopathy 51 1.391
275
P ENT005 Entropion 34 1.380
276
CRH001 Crohn's Disease 80 1.375
277
P HYP040 Hypospadias 51 1.373
278
TRG002 Trigeminal Neuralgia 61 1.367
279
ALL006 Allergic Asthma 56 1.354
280
c VSC019 Vesicoureteral Reflux 1 56 1.343
281
CRT015 Carotid Artery Occlusion 45 1.333
282
P DYS154 Dystonia 64 1.322
283
NPH091 Nephrolithiasis, Calcium Oxalate 61 1.316
284
P PLY019 Polyneuropathy 53 1.312
285
ANL022 Anal Fistula 47 1.311
286
ACL001 Acalculous Cholecystitis 34 1.310
287
BRN004 Brain Edema 54 1.303
288
PRT251 Proteinuria, Chronic Benign 58 1.301
289
BRN038 Bronchial Disease 51 1.295
290
P LKM002 Leukemia 66 1.295
291
c ACT073 Acute Leukemia 59 1.295
292
c LKM061 Leukemia, Acute Myeloid 83 1.295
293
IMP005 Impotence 52 1.290
294
RTR001 Retrograde Amnesia 41 1.290
295
MCN017 Meconium Ileus 52 1.279
296
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 1.279
297
HRP004 Herpes Zoster 60 1.277
298
P RTN016 Retinal Degeneration 52 1.272
299
CHL004 Cholelithiasis 48 1.271
300
ASP007 Aspiration Pneumonia 49 1.269
301
P ANP001 Anaplastic Large Cell Lymphoma 61 1.265
302
MRP001 Morphine Dependence 41 1.265
303
P SCL057 Scoliosis, Isolated 1 40 1.263
304
P PTS002 Ptosis 52 1.263
305
P ENC004 Encephalitis 61 1.253
306
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 1.252
307
RBS001 Rabies 58 1.244
308
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 1.244
309
RTN003 Retinal Ischemia 48 1.244
310
P VSC011 Vasculitis 61 1.239
311
P HYD006 Hydrocephalus 63 1.226
312
HMN044 Human Immunodeficiency Virus Type 1 76 1.225
313
SVR001 Severe Acute Respiratory Syndrome 68 1.225
314
P ESS003 Essential Thrombocythemia 68 1.225
315
P PLY018 Polycythemia 56 1.225
316
P ATT013 Attention Deficit-Hyperactivity Disorder 66 1.224
317
PRT037 Pertussis 49 1.213
318
P HYP265 Hypotonia 42 1.213
319
P PNM007 Pneumonia 64 1.212
320
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 1.194
321
P ERY008 Erythromelalgia 50 1.181
322
NPH009 Nephrolithiasis 54 1.181
323
c CHR087 Chronic Cystitis 37 1.145
324
PYR004 Pyuria 36 1.133
325
ADG002 Audiogenic Seizures 25 1.130
326
PLY001 Polycythemia Vera 69 1.129
327
MYL005 Myelofibrosis 70 1.129
328
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 36 1.129
329
MYL009 Myelodysplastic Syndrome 67 1.129
330
TND004 Tendinopathy 45 1.129
331
TND005 Tendinitis 54 1.129
332
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 47 1.129
333
SPL004 Splenic Marginal Zone Lymphoma 50 1.129
334
PRL017 Prolymphocytic Leukemia 47 1.129
335
NSP002 Nasopharyngitis 45 1.129
336
c PRM012 Primary Polycythemia 58 1.129
337
ART074 Aortic Dissection 53 1.129
338
CHR563 Chronic Eosinophilic Leukemia 48 1.129
339
P NJM001 Nijmegen Breakage Syndrome 75 1.129
340
P LYM118 Lymphoma 69 1.129
341
P INT260 Intracranial Berry Aneurysm 39 1.129
342
P LYM033 Lymphoproliferative Syndrome 59 1.129
343
c EHL080 Ehlers-Danlos Syndrome, Musculocontractural Type, 1 53 1.129
344
P CMP005 Campomelic Dysplasia 65 1.129
345
MST024 Mastocytosis, Cutaneous 66 1.129
346
P OCL013 Oculodentodigital Dysplasia 67 1.129
347
NLP001 Nail-Patella Syndrome 63 1.129
348
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 43 1.129
349
HLS003 Helsmoortel-Van Der Aa Syndrome 48 1.129
350
MNN028 Mononeuropathy of the Median Nerve, Mild 46 1.129
351
ALN001 Aland Island Eye Disease 55 1.129
352
BRD004 Borderline Personality Disorder 53 1.129
353
P CRP001 Carpal Tunnel Syndrome 66 1.129
354
c THR090 Thrombocythemia 1 50 1.129
355
CHR286 Chronic Neutrophilic Leukemia 42 1.129
356
P CHR285 Chronic Myelomonocytic Leukemia 59 1.129
357
NRD100 Neurodevelopmental, Jaw, Eye, and Digital Syndrome 49 1.129
358
END041 Endometrial Adenocarcinoma 63 1.129
359
ACQ007 Acquired Immunodeficiency Syndrome 58 1.129
360
PLS009 Plasma Cell Neoplasm 64 1.129
361
MYL075 Myelodysplastic/myeloproliferative Neoplasm 51 1.129
362
MYL031 Myeloproliferative Neoplasm 66 1.129
363
PLM022 Pulmonary Valve Insufficiency 45 1.129
364
LNG031 Lung Benign Neoplasm 51 1.129
365
CLN045 Colonic Benign Neoplasm 48 1.129
366
HMT002 Hematologic Cancer 61 1.129
367
EXT010 Extramedullary Plasmacytoma 46 1.129
368
RSP006 Respiratory System Disease 51 1.129
369
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 35 1.129
370
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 43 1.129
371
PST046 Post-Transplant Lymphoproliferative Disease 53 1.129
372
RFR002 Refractory Hairy Cell Leukemia 34 1.129
373
P THY032 Thyroiditis 56 1.129
374
P MXD050 Mixed Phenotype Acute Leukemia 45 1.129
375
PRS011 Persian Gulf Syndrome 35 1.129
376
BNM001 Bone Marrow Cancer 45 1.129
377
c ALM001 Al Amyloidosis 54 1.129
378
P MST002 Mast-Cell Leukemia 50 1.129
379
INT054 Intraocular Lymphoma 48 1.129
380
GST050 Gastrointestinal System Disease 55 1.129
381
P FML364 Familial Thoracic Aortic Aneurysm and Aortic Dissection 71 1.129
382
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 1.129
383
P PRD037 Periodontal Ehlers-Danlos Syndrome 44 1.129
384
49X006 49, Xxxxy Syndrome 40 1.129
385
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 1.129
386
P GLM040 Glioma Susceptibility 1 70 1.120
387
MLG169 Malignant Astrocytoma 57 1.120
388
EXP004 Exophthalmos 50 1.120
389
INF118 Inflammatory Myopathy with Abundant Macrophages 27 1.120
390
CLT003 Colitis 63 1.111
391
P GST053 Gastric Cancer 82 1.106
392
P ENC018 Encephalopathy 62 1.102
393
URL001 Urolithiasis 45 1.100
394
PRP083 Porphyria, Acute Intermittent 64 1.095
395
P LCT001 Lactic Acidosis 50 1.092
396
P MCR129 Microvascular Complications of Diabetes 1 68 1.089
397
c BPL002 Bipolar I Disorder 47 1.086
398
CNT097 Central Hypoventilation Syndrome, Congenital 70 1.079
399
CRD137 Cardiogenic Shock 56 1.077
400
SPN369 Spinal Disease 43 1.067
401
P PNC025 Panic Disorder 52 1.061
402
P PRK039 Parkinsonism 55 1.050
403
P MYP004 Myopathy 67 1.050
404
END086 End Stage Renal Disease 54 1.050
405
P EPD009 Epidermolysis Bullosa Dystrophica 66 1.045
406
INT323 Intraocular Pressure Quantitative Trait Locus 63 1.039
407
SVR004 Severe Combined Immunodeficiency 71 1.039
408
P CRV039 Cervicitis 52 1.028
409
IFP003 Ifap Syndrome 2 42 1.027
410
c PLM164 Pulmonary Hypertension, Primary, 1 80 1.027
411
NRM004 Neuroma 49 1.027
412
ULC004 Ulcerative Colitis 74 1.027
413
PRT013 Portal Hypertension 59 1.015
414
P MGR003 Migraine with Aura 51 1.015
415
CHL014 Cholera 62 1.015
416
P OBS001 Obstructive Jaundice 49 1.015
417
DYS073 Dysphagia 53 1.015
418
BP1002 Bap1 Tumor Predisposition Syndrome 42 1.015
419
TRD006 Tardive Dyskinesia 53 1.009
420
P HNT016 Huntington Disease 73 1.003
421
HYD005 Hydrocele 46 1.003
422
DBT002 Diabetic Autonomic Neuropathy 40 0.993
423
P BLD134 Bladder Cancer 79 0.991
424
P LKM062 Leukemia, Acute Lymphoblastic 69 0.991
425
HMR023 Hemorrhagic Cystitis 43 0.991
426
CLF027 Cleft Palate, Isolated 64 0.991
427
P HYP061 Hypertrophic Cardiomyopathy 69 0.991
428
APP008 Appendicitis 62 0.991
429
DRG024 Drug Allergy 40 0.988
430
CHL068 Cholestasis 61 0.988
431
MDD018 Middle East Respiratory Syndrome 44 0.978
432
SBS004 Substance Dependence 46 0.978
433
c CNT068 Central Pain Syndrome 28 0.978
434
THY029 Thyroid Carcinoma 54 0.978
435
P INF037 Inflammatory Bowel Disease 53 0.964
436
OST003 Osteonecrosis 61 0.964
437
PCT003 Pectus Excavatum 43 0.964
438
PLP001 Pulpitis 48 0.950
439
SPN020 Spondylosis 46 0.950
440
P PRD008 Periodontitis 64 0.950
441
OST115 Osteonecrosis of the Jaw 40 0.950
442
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.943
443
ESP021 Esophageal Cancer 84 0.935
444
P OST002 Osteoporosis 77 0.935
445
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.935
446
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.935
447
SPN392 Spondylosis, Cervical 30 0.935
448
P MYP006 Myopia 55 0.935
449
AGR002 Agoraphobia 45 0.935
450
CSL001 Causalgia 44 0.935
451
RDN001 Reading Disorder 40 0.933
452
ALL003 Allergic Rhinitis 66 0.920
453
SRT004 Serotonin Syndrome 54 0.920
454
GLM045 Glioma 62 0.907
455
GLL048 Glial Tumor 52 0.907
456
PLL012 Pollen Allergy 44 0.903
457
KRT008 Keratopathy 46 0.903
458
P URT039 Urticaria 57 0.903
459
P RCT021 Rectum Cancer 54 0.894
460
P ALZ034 Alzheimer Disease 87 0.886
461
DWN001 Down Syndrome 70 0.886
462
c CRD065 Cardiomyopathy, Familial Hypertrophic, 2 48 0.886
463
PHY002 Physical Disorder 41 0.886
464
P PNC035 Pancreatic Cancer 86 0.886
465
P MYT002 Myotonic Dystrophy 51 0.886
466
CNN001 Cannabis Dependence 38 0.878
467
CNN002 Cannabis Abuse 44 0.878
468
P PRR016 Pierre Robin Syndrome 50 0.867
469
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.867
470
URT010 Ureteral Obstruction 45 0.867
471
P ECL001 Eclampsia 52 0.867
472
CHR178 Chromosomal Triplication 34 0.867
473
CRC006 Carcinoid Syndrome 55 0.867
474
ACR008 Acrocallosal Syndrome 70 0.864
475
MSC007 Muscle Hypertrophy 64 0.864
476
P ESP024 Esophagitis 60 0.864
477
LVR012 Liver Cirrhosis 62 0.863
478
PPT005 Peptic Ulcer Disease 58 0.863
479
PRS045 Prostatic Hypertrophy 52 0.854
480
GRG001 Greig Cephalopolysyndactyly Syndrome 64 0.846
481
ASP008 Aspiration Pneumonitis 43 0.846
482
GTR002 Goiter 52 0.846
483
ISL075 Isolated Pierre Robin Sequence 29 0.846
484
PRS021 Prostatic Adenoma 43 0.842
485
CRD001 Cardiac Tamponade 44 0.842
486
P NRC002 Narcolepsy 55 0.842
487
PRS129 Prostatic Hyperplasia, Benign 48 0.830
488
PRP016 Paraplegia 52 0.830
489
P MYC008 Myocarditis 59 0.830
490
WHP002 Whiplash 35 0.830
491
PNM010 Pneumothorax, Primary Spontaneous 58 0.824
492
CHL013 Cholecystolithiasis 37 0.824
493
BLR001 Biliary Atresia 55 0.824
494
P SCL009 Sclerosing Cholangitis 46 0.824
495
ART006 Arthus Reaction 40 0.824
496
HYP005 Hypokalemia 55 0.824
497
IMM206 Immune Complex Mediated Vasculitis 13 0.824
498
ANG054 Angina Pectoris 65 0.818
499
INT067 Interstitial Nephritis 47 0.818
500
c ATR087 Atrial Standstill 1 74 0.818
501
CRD132 Cardiac Conduction Defect 59 0.818
502
LWC001 Low Compliance Bladder 44 0.818
503
BRN002 Bronchiolitis 57 0.818
504
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 25 0.806
505
P ANG015 Angioedema 56 0.798
506
P CRB088 Cerebral Atrophy 33 0.798
507
c SCN059 Secondary Sclerosing Cholangitis 21 0.798
508
AMB002 Amblyopia 49 0.793
509
SPP007 Suppression Amblyopia 38 0.793
510
FCL014 Focal Epilepsy 53 0.793
511
IRR002 Irritable Bowel Syndrome 65 0.793
512
P MYC007 Myocardial Infarction 69 0.779
513
HRW001 Hair Whorl 35 0.779
514
ATR057 Atrioventricular Block 54 0.779
515
CRB090 Cerebral Hypoxia 42 0.779
516
c BCT013 Bacterial Pneumonia 47 0.779
517
ETN001 Eating Disorder 59 0.779
518
P RST001 Restless Legs Syndrome 52 0.768
519
ASY002 Asymptomatic Neurosyphilis 41 0.768
520
P TRC072 Treacher Collins Syndrome 1 62 0.768
521
NRS003 Neurosyphilis 45 0.768
522
LWR018 Lower Urinary Tract Obstruction, Congenital 39 0.767
523
DSS032 Disease by Infectious Agent 55 0.767
524
DFN344 Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome 55 0.767
525
P URF003 Urofacial Syndrome 1 56 0.767
526
ANG049 Angioedema Induced by Ace Inhibitors 39 0.767
527
GST020 Gastric Antral Vascular Ectasia 40 0.767
528
URN009 Urinary System Disease 47 0.767
529
ATR089 Atrioventricular Dissociation 21 0.765
530
c DLT002 Dilated Cardiomyopathy 79 0.765
531
ATN005 Autonomic Dysfunction 45 0.765
532
SPS057 Spasticity 43 0.765
533
c ATM075 Autoimmune Encephalitis 39 0.765
534
RBR002 Roberts-Sc Phocomelia Syndrome 63 0.763
535
P SPP010 Suppressor of Tumorigenicity 3 51 0.750
536
P LNG064 Lung Cancer Susceptibility 3 70 0.750
537
CRD223 Cardiac Arrhythmia 63 0.750
538
MLC004 Mulchandani-Bhoj-Conlin Syndrome 51 0.750
539
ASP004 Asphyxia Neonatorum 50 0.750
540
c SCH085 Schizophrenia 2 27 0.750
541
BLR004 Biliary Dyskinesia 36 0.750
542
GST039 Gastroduodenitis 37 0.750
543
P HYP098 Hypereosinophilic Syndrome 66 0.750
544
PST048 Postural Orthostatic Tachycardia Syndrome 46 0.734
545
P OVR042 Ovarian Cancer 88 0.734
546
DNT046 Dental Abscess 32 0.734
547
PHB003 Phobia, Specific 44 0.734
548
TMT002 Temtamy Preaxial Brachydactyly Syndrome 54 0.734
549
BRC012 Brucellosis 66 0.734
550
GLB002 Glioblastoma 67 0.734
551
TST014 Testicular Cancer 51 0.734
552
P NRF002 Neurofibromatosis 60 0.734
553
P PRS040 Prostate Cancer 95 0.728
554
QTN001 Qt Interval, Variation in 12 0.728
555
CRD220 Cardiac Valvular Defect, Developmental 29 0.728
556
ADN002 Adenoiditis 36 0.728
557
c PRS130 Prostate Cancer, Hereditary, 8 32 0.728
558
c PRS136 Prostate Cancer, Hereditary, 6 33 0.728
559
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 57 0.728
560
ADN067 Adenoid Hypertrophy 39 0.728
561
ANS012 Anus Disease 47 0.728
562
DVR001 Diverticulitis of Colon 24 0.728
563
DRG001 Drug Psychosis 29 0.728
564
CHL012 Childhood Disintegrative Disease 44 0.728
565
AGG012 Aggressive Nk-Cell Leukemia 47 0.728
566
P ART023 Arthropathy 60 0.728
567
ATY005 Atypical Teratoid Rhabdoid Tumor 69 0.728
568
TMP019 Temporomandibular Joint Anomaly 28 0.728
569
ORB013 Orbital Disease 42 0.728
570
DVR002 Diverticulitis 46 0.728
571
CLF049 Cleft Lip and Alveolus 32 0.728
572
P PTT006 Pituitary Adenoma 55 0.728
573
LWF001 Low-Flow Priapism 16 0.728
574
c DMN005 Diamond-Blackfan Anemia 2 28 0.718
575
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.718
576
RTN017 Retinal Detachment 60 0.718
577
LNG073 Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 58 0.718
578
P HRS035 Hirschsprung Disease 1 66 0.718
579
PLT031 Platelet Membrane Fluidity 28 0.718
580
c PRM093 Premature Ovarian Failure 7 47 0.718
581
P CRN026 Corneal Edema 42 0.718
582
HPT004 Hepatic Coma 43 0.718
583
SYR010 Syringomyelia, Noncommunicating Isolated 36 0.718
584
PRP027 Peripheral Vascular Disease 71 0.718
585
RTN020 Retinal Vascular Disease 45 0.718
586
HPT019 Hepatic Encephalopathy 59 0.718
587
HMP001 Hemopericardium 47 0.718
588
P ART021 Arteriosclerosis 53 0.718
589
GLM008 Glomus Tumor 48 0.718
590
P SYR001 Syringomyelia 47 0.718
591
P PTN014 Patent Ductus Arteriosus 1 59 0.718
592
CRB086 Cerebral Aneurysms 40 0.718
593
SYN036 Syncope 44 0.718
594
CYC008 Cyclic Vomiting Syndrome 46 0.701
595
VSC052 Vasculitis, Lymphocytic, Nodular 23 0.701
596
BNR002 Bone Resorption Disease 47 0.701
597
P MYM013 Moyamoya Disease 1 60 0.701
598
SNN002 Sinonasal Undifferentiated Carcinoma 30 0.701
599
CLC001 Calciphylaxis 50 0.701
600
P MCR010 Microcephaly 59 0.701
601
GLS004 Glossopharyngeal Neuralgia 37 0.701
602
HYP264 Hypertonia 36 0.701
603
PST092 Posttransplant Acute Limbic Encephalitis 29 0.701
604
c ACT134 Acute Liver Failure 57 0.701
605
HMC014 Homocysteinemia 52 0.682
606
P FML340 Familial Episodic Pain Syndrome 50 0.682
607
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.682
608
DDN010 Duodenum Cancer 52 0.682
609
MND002 Mandibuloacral Dysplasia with Type B Lipodystrophy 37 0.682
610
PPL052 Papillomatosis, Confluent and Reticulated 34 0.682
611
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.682
612
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.682
613
TST015 Testicular Disease 42 0.682
614
BLR002 Bile Reflux 38 0.682
615
P PRC012 Pericardial Effusion 50 0.682
616
TRN015 Transient Cerebral Ischemia 62 0.682
617
URC005 Urachal Cyst 25 0.682
618
NRM005 Neuromuscular Disease 63 0.682
619
P THL005 Thalassemia 56 0.682
620
P INS002 in Situ Carcinoma 53 0.682
621
ART008 Arteriosclerosis Obliterans 40 0.682
622
HYP144 Hyperacusis 23 0.682
623
P RTN024 Retinoblastoma 72 0.661
624
LYM133 Lymphoma, Hodgkin, Classic 74 0.661
625
P MYS003 Myasthenia Gravis 68 0.661
626
P TRT019 Torticollis 47 0.661
627
CRV035 Cervical Cancer 72 0.661
628
LYM143 Lymphoma, Non-Hodgkin, Familial 79 0.661
629
PLY183 Polymicrogyria with or Without Vascular-Type Ehlers-Danlos Syndrome 41 0.661
630
CRN288 Corneal Dystrophy, Band-Shaped 36 0.661
631
P BRG001 Brugada Syndrome 69 0.661
632
P RCS002 Recessive Dystrophic Epidermolysis Bullosa 62 0.661
633
OCL052 Ocular Dominance 40 0.661
634
INT258 Interstitial Nephritis, Karyomegalic 45 0.661
635
HMP005 Hemiplegia 53 0.661
636
P LSS002 Lissencephaly 53 0.661
637
P ALT001 Alternating Hemiplegia of Childhood 56 0.661
638
P TRC087 Tricuspid Valve Disease 48 0.661
639
MST005 Mastitis 52 0.661
640
P UVT001 Uveitis 57 0.661
641
c ACT068 Acute Cystitis 61 0.661
642
RCT020 Rectum Adenocarcinoma 48 0.661
643
HYP016 Hypochondriasis 47 0.661
644
CHR020 Chronic Interstitial Cystitis 36 0.661
645
CNV002 Conversion Disorder 47 0.661
646
ASP003 Aseptic Meningitis 51 0.661
647
ERL001 Early Myoclonic Encephalopathy 63 0.661
648
P BRS044 Breast Adenocarcinoma 58 0.661
649
CPH001 Cephalic Disorders 6 0.661
650
PLY024 Polymicrogyria 46 0.661
651
P MTC133 Mitochondrial Myopathy 51 0.661
652
STC004 Stachybotrys Chartarum 33 0.661
653
SPL018 Splenomegaly 47 0.661
654
CHL078 Childhood-Onset Schizophrenia 29 0.661
655
RFR003 Refractive Error 41 0.661
656
HRN003 Heroin Dependence 44 0.661
657
NWD001 New Daily-Persistent Headache 19 0.661
658
SNK001 Snakebite Envenomation 22 0.661
659
CHR072 Chordoma 57 0.639
660
c SCH051 Schizophrenia 4 35 0.639
661
DFF005 Diffuse Large B-Cell Lymphoma 55 0.639
662
P GRF003 Graft-Versus-Host Disease 71 0.639
663
LNN001 Lennox-Gastaut Syndrome 61 0.639
664
P MDL005 Medulloblastoma 75 0.639
665
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.639
666
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.639
667
P FML023 Familial Hemiplegic Migraine 53 0.639
668
NRL016 Neural Tube Defects 81 0.639
669
HND015 Hand Skill, Relative 29 0.639
670
LCH016 Lichen Sclerosus Et Atrophicus 41 0.639
671
P BNC003 Bone Cancer 58 0.639
672
KRT001 Keratoconjunctivitis Sicca 49 0.639
673
ANK001 Ankylosis 51 0.639
674
P LTR001 Lateral Sclerosis 58 0.639
675
DBT004 Diabetic Polyneuropathy 50 0.639
676
P EHL001 Ehlers-Danlos Syndrome 57 0.639
677
ATY001 Atypical Depressive Disorder 45 0.639
678
BRN009 Burning Mouth Syndrome 51 0.639
679
P ORT004 Orthostatic Intolerance 62 0.639
680
KRT006 Keratoconjunctivitis 53 0.639
681
c ACT075 Acute Myocardial Infarction 55 0.639
682
P PMP001 Pemphigus 55 0.639
683
P HMN010 Hemangioma 61 0.632
684
OBS082 Obstructive Nephropathy 41 0.632
685
P SRC025 Sarcoidosis 1 70 0.613
686
CPR004 Coproporphyria, Hereditary 57 0.613
687
PRC054 Perching Syndrome 33 0.613
688
HYP025 Hyperphosphatemia 47 0.613
689
HYP017 Hypophosphatemia 49 0.613
690
ANS006 Anosognosia 34 0.613
691
c PCH015 Pachyonychia Congenita 1 60 0.613
692
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.613
693
PRN049 Paraneoplastic Pemphigus 44 0.613
694
CRY004 Cryoglobulinemia 47 0.613
695
P LMY004 Leiomyosarcoma 62 0.613
696
KRT009 Keratosis 52 0.613
697
NRN004 Neuroendocrine Tumor 55 0.613
698
TYP007 Typhoid Fever 63 0.613
699
ALT003 Alternating Exotropia 33 0.613
700
EXT022 Exotropia 42 0.613
701
BLR008 Bilirubin Metabolic Disorder 57 0.613
702
EGG001 Egg Allergy 41 0.613
703
TMP006 Temporomandibular Ankylosis 19 0.613
704
STM007 Stomatitis 52 0.613
705
TXC010 Toxic Myocarditis 21 0.613
706
CRY036 Cryptogenic Cirrhosis 36 0.613
707
P LPS004 Lupus Erythematosus 61 0.613
708
PSD088 Pseudobulbar Affect 33 0.613
709
PRR019 Perioral Myoclonia with Absences 27 0.613
710
P LNG028 Long Qt Syndrome 63 0.601
711
MYC080 Myoclonic Epilepsy of Unverricht and Lundborg 52 0.582
712
P DST002 Distal Arthrogryposis 63 0.582
713
P PLY014 Polycystic Kidney Disease 71 0.582
714
MCR037 Macroglossia 44 0.582
715
P PRK057 Parkinson Disease, Late-Onset 79 0.582
716
MNN047 Mannosidosis, Alpha B, Lysosomal 67 0.582
717
BNG091 Benign Chronic Pemphigus 56 0.582
718
VRG001 Variegate Porphyria 55 0.582
719
ECT026 Ectopic Pregnancy 47 0.582
720
ADN018 Adenoma 58 0.582
721
NRN001 Neuroendocrine Carcinoma 47 0.582
722
SPR017 Spermatocele 35 0.582
723
P HYP263 Hypersomnia 40 0.582
724
P FBR031 Febrile Seizures 52 0.582
725
FLP002 Floppy Infant Syndrome 13 0.582
726
ACH005 Achalasia 54 0.582
727
CNT015 Central Sleep Apnea 46 0.582
728
PRL008 Paralytic Ileus 44 0.582
729
EPL230 Epilepsy with Myoclonic-Atonic Seizures 23 0.582
730
OPS006 Opsoclonus-Myoclonus Syndrome 48 0.582
731
CNG506 Congenital Amyoplasia 27 0.582
732
P INT070 Intestinal Obstruction 57 0.580
733
WLF001 Wolff-Parkinson-White Syndrome 63 0.543
734
c NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 66 0.543
735
TRC097 Tracheomalacia 43 0.543
736
c CTR103 Cataract 4, Multiple Types 49 0.543
737
c MYT021 Myotonic Dystrophy 1 67 0.543
738
THR024 Thrombosis 56 0.543
739
LMY002 Leiomyoma 51 0.543
740
CRB027 Cerebellar Disease 47 0.543
741
PLM001 Pulmonary Tuberculosis 69 0.543
742
P DMN002 Dementia 65 0.543
743
LYM017 Lyme Disease 63 0.543
744
P MST009 Mastocytosis 64 0.543
745
MYF001 Myofibroma 42 0.543
746
P DYS021 Dysautonomia 38 0.543
747
P BLR006 Biliary Tract Disease 46 0.543
748
FTD001 Foot Drop 36 0.543
749
PRF003 Piriformis Syndrome 24 0.543
750
P SPN236 Spina Bifida Cystica 22 0.543
751
MDS022 Mediastinitis 47 0.462
752
CRN030 Coronary Stenosis 50 0.462
754
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 0.447
755
CRV043 Cervical Dystonia 45 0.447
756
ACH004 Achondroplasia 66 0.447
757
NVS017 Nevus, Epidermal 66 0.447
758
WLL001 Williams-Beuren Syndrome 60 0.447
759
HYP060 Hyperinsulinism 53 0.447
760
CVR006 Cavernous Hemangioma 51 0.447
761
CPG001 Capgras Syndrome 26 0.447
762
CHR073 Choreatic Disease 53 0.447
763
PNT003 Pinta Disease 30 0.447
764
SYS004 Systemic Mastocytosis 62 0.447
765
INT025 Intermittent Explosive Disorder 39 0.447
766
P EPL003 Epulis 30 0.447
767
MYC032 Myoclonic Encephalopathy of Infants 10 0.447
768
NPH001 Nephrogenic Adenoma 30 0.447
769
DWR001 Dwarfism 45 0.447
770
ACY011 Acyl-Coa Dehydrogenase Deficiency 31 0.447
771
GST092 Gastroesophageal Reflux 60 0.429
772
c MCL046 Mucolipidosis Iii Alpha/beta 61 0.366
773
RSP027 Respiratory Papillomatosis, Juvenile Recurrent, Congenital 47 0.366
774
SCR035 Sacral Agenesis with Vertebral Anomalies 39 0.366
775
HYP458 Hyper Ige Syndrome 60 0.366
776
c VRL005 Viral Pneumonia 52 0.366
777
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 0.366
778
RSP021 Respiratory Allergy 41 0.366
779
P CRC039 Coarctation of Aorta 46 0.366
780
PLY105 Polycystic Ovary Syndrome 1 39 0.366
781
INT030 Intracranial Aneurysm 55 0.366
782
BRS099 Breast Ductal Carcinoma 61 0.366
783
P PLY011 Polycystic Ovary Syndrome 57 0.366
784
c CNT035 Central Nervous System Disease 53 0.366
785
BRS051 Breast Disease 58 0.366
786
c XNT010 Xanthinuria, Type I 52 0.366
787
SDD004 Sudden Arrhythmia Death Syndrome 22 0.366
788
P DBT009 Diabetes Mellitus 67 0.359
789
TST044 Testicular Torsion 45 0.318
790
SCH012 Schizoaffective Disorder 49 0.303
791
P HYP086 Hypothyroidism 69 0.303
792
P SYP003 Syphilis 59 0.303
793
P FTL001 Fetal Alcohol Syndrome 55 0.288
795
MTN003 Motion Sickness 50 0.288
796
SNG003 Single Ventricular Heart 30 0.288
797
c SCH079 Schizophrenia 1 44 0.271
798
P END044 Endometriosis 62 0.271
799
P MVM001 Movement Disease 61 0.271
800
MTR002 Mitral Valve Insufficiency 51 0.271
801
OCL006 Ocular Hypertension 53 0.271
802
GLC003 Glucose Intolerance 53 0.254
803
P DXT004 Dextro-Looped Transposition of the Great Arteries 58 0.254
804
INT051 Intussusception 53 0.254
805
ATM095 Autoimmune Disease 61 0.254
806
c VRL007 Viral Encephalitis 50 0.254
807
TRC022 Tricuspid Valve Insufficiency 47 0.254
808
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.254
809
GLY010 Glycine Encephalopathy 57 0.235
810
BCT022 Bacterial Infectious Disease 56 0.235
811
P WLF004 Wolfram Syndrome 61 0.235
812
c WLF013 Wolfram Syndrome 1 60 0.235
813
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.235
814
P INF032 Infertility 60 0.235
815
BRN024 Bronchitis 67 0.235
816
PLM041 Pulmonary Valve Stenosis 50 0.235
817
P ART018 Aortic Valve Insufficiency 52 0.235
818
MGC001 Megacolon 48 0.235
819
DYS011 Dyskinesia of Esophagus 40 0.235
820
P ANG001 Angelman Syndrome 65 0.214
821
c ART101 Aortic Valve Disease 2 65 0.214
822
BRN014 Bronchopneumonia 52 0.214
823
P DRR001 Diarrhea 55 0.214
824
QDR001 Quadriplegia 49 0.214
825
P DDN001 Duodenal Ulcer 53 0.214
826
TXC001 Toxic Megacolon 37 0.214
827
CDQ001 Cauda Equina Syndrome 37 0.214
828
P PLM036 Pulmonary Fibrosis 65 0.214
829
P GLY013 Glycogen Storage Disease 59 0.214
830
P MSC003 Muscular Atrophy 52 0.214
831
PRS064 Persistent Vegetative State 33 0.214
832
P CMP008 Compartment Syndrome 50 0.214
833
CHC001 Chickenpox 56 0.214
834
BNG077 Benign Idiopathic Neonatal Seizures 22 0.214
835
VRC005 Varicose Veins 59 0.192
836
c MCR245 Microphthalmia, Syndromic 8 46 0.192
837
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 0.192
838
HYP020 Hyperprolactinemia 63 0.192
839
MCR013 Microphthalmia 60 0.192
840
NRF028 Near-Fatal Asthma 26 0.192
841
OTT002 Otitis Media 71 0.192
842
SPS007 Spastic Cerebral Palsy 46 0.192
843
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 44 0.192
844
c CRN139 Cornelia De Lange Syndrome 1 61 0.192
845
PTH002 Pathological Gambling 48 0.192
846
LPD008 Lipid Metabolism Disorder 61 0.192
847
P CRN015 Cornelia De Lange Syndrome 67 0.192
848
P TCD001 Tic Disorder 50 0.192
849
HGH001 High Pressure Neurological Syndrome 28 0.192
850
P RHB003 Rhabdomyosarcoma 66 0.192
851
PRS063 Paresthesia 39 0.192
852
NNT008 Neonatal Abstinence Syndrome 40 0.192
853
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.192
854
MCP033 Mucopolysaccharidoses 44 0.192
855
P INF038 Influenza 68 0.192
856
PLM033 Pulmonary Embolism 58 0.192
857
GRN017 Granulocytopenia 42 0.192
858
P HYP055 Hypoplastic Left Heart Syndrome 65 0.192
859
P SNS001 Sensorineural Hearing Loss 59 0.166
860
c GLY008 Glycogen Storage Disease Ii 72 0.166
861
INT303 Intracranial Hypertension, Idiopathic 56 0.166
862
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.166
863
P HYP750 Hypertriglyceridemia, Familial 62 0.166
864
FCL074 Facial Spasm 19 0.166
865
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 50 0.166
866
c WLM017 Wilms Tumor 4 18 0.166
867
c DVL034 Developmental and Epileptic Encephalopathy 3 45 0.166
868
SPN354 Spinal Arachnoiditis 35 0.166
869
P OPT006 Optic Nerve Disease 57 0.166
870
OST017 Osteomyelitis 63 0.166
871
ANS004 Anisometropia 31 0.166
872
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.166
873
P HML002 Hemolytic Anemia 62 0.166
874
PLR005 Pleuropneumonia 33 0.166
875
HMS001 Hemosiderosis 48 0.166
876
ARC002 Arachnoiditis 49 0.166
877
GST023 Gastric Ulcer 52 0.166
878
P NPH012 Nephrotic Syndrome 62 0.166
879
P GLM007 Glomerulonephritis 59 0.166
880
GLS001 Gliosarcoma 63 0.166
881
SKN005 Skin Atrophy 41 0.166
882
WLL004 Wallerian Degeneration 38 0.166
883
OCL010 Ocular Hypotension 36 0.166
885
P TRC031 Trichorhinophalangeal Syndrome 37 0.166
886
P AMY004 Amyloidosis 69 0.166
887
P HYP076 Hyperthyroidism 53 0.166
888
MLG086 Malignant Hyperthermia Susceptibility 39 0.166
889
ESN011 Eisenmenger Syndrome 46 0.166
890
NWN001 New-Onset Refractory Status Epilepticus 22 0.166
892
c RRP028 Rare Epilepsy 17 0.166
893
CHD001 Chediak-Higashi Syndrome 67 0.136
894
c HMP029 Hemophilia a 69 0.136
895
ORN008 Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to 61 0.136
896
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 59 0.136
897
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.136
898
c LNG047 Long Qt Syndrome 2 58 0.136
899
ALV005 Alveolar Soft Part Sarcoma 61 0.136
900
HLX001 Helix Syndrome 47 0.136
901
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 0.136
902
c PCH010 Pachyonychia Congenita 3 43 0.136
903
MLD018 Mild Cognitive Impairment 48 0.136
904
c PRC016 Pre-Eclampsia 64 0.136
905
RCK004 Rickets 65 0.136
906
PLV003 Pelvic Inflammatory Disease 54 0.136
907
P END033 Endocarditis 58 0.136
908
PLY150 Polykaryocytosis Inducer 29 0.136
909
c HYD064 Hydrocephalus, Congenital, 1 51 0.136
910
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.136
911
MCK005 Mckusick-Kaufman Syndrome 61 0.136
912
INF034 Infective Endocarditis 53 0.136
913
LMB062 Limb Ischemia 55 0.136
914
P ATR011 Atrial Fibrillation 66 0.136
915
ERY003 Erythema Multiforme 56 0.136
916
SVR097 Severe Cutaneous Adverse Reaction 68 0.136
917
BRT054 Brittle Bone Disorder 74 0.136
918
P LRY029 Laryngomalacia 47 0.136
919
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.136
920
c PRG042 Progressive Familial Heart Block, Type Ia 65 0.136
921
TRT017 Teratoma, Ovarian 28 0.136
922
FCT001 Factor Viii Deficiency 62 0.136
923
c SCL052 Scleroderma, Familial Progressive 60 0.136
924
HRN029 Hearing Loss, Noise-Induced 37 0.136
925
GLL008 Gilles De La Tourette Syndrome 64 0.136
926
c DPH024 Diaphragmatic Hernia, Congenital 64 0.136
927
P PRD006 Prader-Willi Syndrome 60 0.136
928
P BND020 Bone Disease 60 0.136
929
P MYS079 Miyoshi Muscular Dystrophy 52 0.136
930
PNS018 Pain Sensitivity Quantitative Trait Locus 1 23 0.136
931
SPC010 Speech and Communication Disorders 48 0.136
932
PRN009 Paranoid Schizophrenia 49 0.136
933
P SCK002 Sick Sinus Syndrome 55 0.136
934
P CND004 Candidiasis 57 0.136
935
MLN003 Melancholia 41 0.136
936
MDD010 Middle Ear Disease 46 0.136
937
P BLP003 Blepharospasm 45 0.136
938
PLC001 Placenta Accreta 44 0.136
939
OVR109 Ovarian Germ Cell Teratoma 32 0.136
940
HDR003 Hidradenitis 50 0.136
941
ACR007 Acromegaly 70 0.136
942
SNS003 Sensory Peripheral Neuropathy 51 0.136
943
P KDN017 Kidney Cancer 60 0.136
944
P FCL005 Focal Segmental Glomerulosclerosis 57 0.136
945
OBS004 Obstructive Hydrocephalus 45 0.136
946
DMP001 Dumping Syndrome 43 0.136
947
P NTR004 Neutropenia 62 0.136
948
NRG002 Neurogenic Bladder 55 0.136
949
PLC005 Placental Insufficiency 56 0.136
950
INS001 Insulinoma 59 0.136
951
CLL003 Cellulitis 53 0.136
952
P FBR017 Fibrosarcoma 55 0.136
953
P RHN004 Rhinitis 57 0.136
954
THR016 Thrombophlebitis 50 0.136
955
P TRT010 Teratoma 50 0.136
956
HDR002 Hidradenitis Suppurativa 54 0.136
957
DMY004 Demyelinating Disease 50 0.136
958
PLR007 Pleural Empyema 51 0.136