Search results for Fentanyl

1407 hits were found for Fentanyl

# Family MCID Name MIFTS Score
1
PNG002 Pain Agnosia 51 57.692
2
P CHR345 Chronic Pain 50 19.518
3
CNS004 Constipation 56 15.617
4
48X005 48,xyyy 39 13.355
5
SBC016 Subacute Delirium 43 12.856
6
c PNS012 Paine Syndrome 60 10.550
7
c EPS039 Episodic Pain Syndrome, Familial, 1 42 10.325
8
AMN003 Amnestic Disorder 54 9.481
9
OPD001 Opioid Abuse 44 8.827
10
BCK006 Back Pain 47 8.717
11
OCL069 Ocular Motor Apraxia 57 8.331
12
P RSP003 Respiratory Failure 74 8.180
13
MCS002 Mucositis 56 8.039
14
OPD006 Opioid Addiction 48 7.268
15
P MYC033 Myoclonus 47 7.043
16
ING001 Inguinal Hernia 59 6.925
17
P SCL018 Scoliosis 57 6.878
18
P CRD119 Cardiac Arrest 67 6.728
19
P SBS003 Substance Abuse 54 6.553
20
P SLP006 Sleep Apnea 69 6.452
21
LPP008 Lipoprotein Quantitative Trait Locus 65 6.400
22
WTH001 Withdrawal Disorder 48 6.250
23
P HDC001 Headache 57 6.201
24
P CTR002 Cataract 60 6.142
25
P TTR001 Tetralogy of Fallot 69 5.909
26
P STR020 Strabismus 56 5.894
27
MCH006 Mechanical Strabismus 40 5.894
28
ART140 Arteries, Anomalies of 53 5.767
29
OST012 Osteoarthritis 77 5.736
30
OPT003 Opiate Dependence 49 5.622
31
SRT004 Serotonin Syndrome 54 5.414
32
CMP010 Complex Regional Pain Syndrome 60 5.337
33
CNG034 Congestive Heart Failure 69 5.323
34
CLF001 Cleft Lip 53 5.251
35
TRM010 Traumatic Brain Injury 51 5.231
36
DYS073 Dysphagia 53 5.198
37
HRT011 Heart Septal Defect 49 5.197
38
PLM010 Pulmonary Edema 55 5.119
39
P EXN002 Exanthem 58 5.065
40
BRN071 Brain Injury 50 5.051
41
LVR012 Liver Cirrhosis 63 5.043
42
P TRM003 Tremor 48 5.033
43
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 4.974
44
PLM129 Pulmonary Disease, Chronic Obstructive 74 4.950
45
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 4.949
46
P VNT002 Ventricular Septal Defect 58 4.942
47
P HRT032 Heart Disease 81 4.923
48
HYP266 Hypoxia 57 4.922
49
ILS001 Ileus 50 4.902
50
P CLR023 Colorectal Cancer 100 4.815
51
c ACT073 Acute Leukemia 58 4.798
52
ALL029 Allergic Disease 59 4.766
53
PST053 Postherpetic Neuralgia 40 4.744
54
TTN003 Tetanus 65 4.622
55
DPR016 Depression 65 4.574
56
LNG099 Lung Disease 62 4.572
57
DRG003 Drug Dependence 46 4.537
58
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 4.516
59
HDN002 Head Injury 44 4.505
60
INT075 Intracranial Hypertension 53 4.490
61
P SZR006 Seizure Disorder 70 4.490
62
P SCK005 Sickle Cell Disease 56 4.351
63
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 4.344
64
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 4.340
65
P BRS047 Breast Cancer 98 4.330
66
APN008 Apnea, Obstructive Sleep 67 4.323
67
MTB004 Metabolic Acidosis 48 4.312
68
PNM008 Pneumothorax 54 4.292
69
CLF004 Cleft Lip/palate 57 4.209
70
c PRC016 Pre-Eclampsia 65 4.190
71
VRS002 Virus-Associated Trichodysplasia Spinulosa 30 4.126
72
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 4.099
73
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 4.099
74
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 4.099
75
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 4.099
76
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 4.099
77
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 4.099
78
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 4.099
79
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 4.099
80
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 4.099
81
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 4.099
82
47X002 47,xyy 48 4.091
83
CYT002 Cytokine Deficiency 43 4.078
84
P ANR048 Aniridia 1 64 4.043
85
P PNC035 Pancreatic Cancer 86 3.993
86
P BNC003 Bone Cancer 58 3.971
87
P GST053 Gastric Cancer 83 3.961
88
ESP021 Esophageal Cancer 83 3.933
89
MNT002 Mental Depression 57 3.900
90
P LNG032 Lung Cancer 98 3.864
91
P PNC044 Pancreatitis 61 3.862
92
P TRN020 Turner Syndrome 67 3.849
93
P LVR013 Liver Disease 69 3.810
94
P MYC007 Myocardial Infarction 70 3.806
95
P NRP001 Neuropathy 60 3.783
96
c MGR028 Migraine with or Without Aura 1 64 3.781
97
CRB086 Cerebral Aneurysms 40 3.756
98
P RCT021 Rectum Cancer 54 3.740
99
PST028 Post-Traumatic Stress Disorder 59 3.726
100
ISC004 Ischemia 61 3.692
101
c ACT027 Acute Pancreatitis 60 3.666
102
P ADL010 Adult Respiratory Distress Syndrome 71 3.666
103
P HYP040 Hypospadias 51 3.659
104
P ATR001 Atrioventricular Septal Defect 55 3.657
105
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 3.644
106
ANX010 Anxiety 70 3.621
107
HRT012 Heart Valve Disease 53 3.616
108
PTH003 Pathologic Nystagmus 52 3.611
109
PCT003 Pectus Excavatum 46 3.596
110
PRT037 Pertussis 65 3.577
111
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 3.567
112
P PHC003 Pheochromocytoma 69 3.557
113
ADR040 Adrenal Gland Pheochromocytoma 46 3.557
114
P PTN014 Patent Ductus Arteriosus 1 59 3.544
115
P NRB001 Neuroblastoma 66 3.544
116
RFL001 Reflex Sympathetic Dystrophy 51 3.543
117
DBT010 Diabetic Neuropathy 54 3.476
118
P LKM002 Leukemia 67 3.474
119
P PLM037 Pulmonary Hypertension 72 3.471
120
c EXD008 Exudative Vitreoretinopathy 1 71 3.471
121
LPT014 Leptin Deficiency or Dysfunction 78 3.379
122
CRB090 Cerebral Hypoxia 42 3.375
123
ART016 Aortic Aneurysm 68 3.370
124
c LKM061 Leukemia, Acute Myeloid 83 3.362
125
CRT015 Carotid Artery Occlusion 45 3.351
126
P ATR011 Atrial Fibrillation 66 3.340
127
AGN016 Aging 54 3.335
128
P CRN300 Coronary Heart Disease 1 73 3.330
129
ATR057 Atrioventricular Block 54 3.328
130
OTT002 Otitis Media 71 3.308
131
FBR047 Fibromyalgia 58 3.271
132
P MLG056 Malignant Hyperthermia 66 3.216
133
HYP066 Hyperglycemia 61 3.210
134
ANR040 Aneurysm 61 3.178
135
P LNG028 Long Qt Syndrome 64 3.143
136
P ENC018 Encephalopathy 62 3.143
137
RHB024 Rhabdomyosarcoma 2 67 3.129
138
RDC002 Radiculopathy 52 3.107
139
NNT008 Neonatal Abstinence Syndrome 40 3.090
140
CYN002 Cyanosis, Transient Neonatal 43 3.077
141
IDP070 Idiopathic Scoliosis 42 3.061
142
SPN369 Spinal Disease 44 3.048
143
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 3.045
144
P PRP019 Peripheral Nervous System Disease 58 3.018
145
PLP001 Pulpitis 48 3.010
146
CRV035 Cervical Cancer 73 3.006
147
ANT019 Anterograde Amnesia 38 2.993
148
TXC005 Toxic Shock Syndrome 62 2.991
149
P HRN001 Horner's Syndrome 46 2.991
150
CLF027 Cleft Palate, Isolated 64 2.959
151
c DLT002 Dilated Cardiomyopathy 78 2.933
152
NPH009 Nephrolithiasis 54 2.917
153
MTN003 Motion Sickness 51 2.916
154
P KDN018 Kidney Disease 72 2.914
155
P MYP004 Myopathy 67 2.904
156
PLM033 Pulmonary Embolism 58 2.893
157
CHL004 Cholelithiasis 49 2.875
158
P DXT004 Dextro-Looped Transposition of the Great Arteries 58 2.870
159
PRS063 Paresthesia 39 2.870
160
SPS057 Spasticity 42 2.831
161
P NRV007 Nervous System Disease 67 2.827
162
DSS032 Disease by Infectious Agent 55 2.813
163
NPH091 Nephrolithiasis, Calcium Oxalate 61 2.804
164
PRT058 Pure Autonomic Failure 58 2.777
165
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 2.729
166
P VSC007 Vascular Disease 63 2.727
167
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 2.722
169
ANX004 Anoxia 40 2.694
170
CRB039 Cerebrovascular Disease 66 2.689
171
ADN027 Adenomyosis 57 2.659
172
PLY150 Polykaryocytosis Inducer 29 2.655
173
OST062 Osteoarthritis with Mild Chondrodysplasia 47 2.624
174
c DPH024 Diaphragmatic Hernia, Congenital 64 2.605
175
P HYP265 Hypotonia 42 2.597
176
P AGN002 Agnosia 54 2.593
177
SPN027 Spinal Stenosis 59 2.585
178
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 2.572
179
P GST044 Gastritis 55 2.559
180
SQM006 Squamous Cell Carcinoma 60 2.550
181
WLF001 Wolff-Parkinson-White Syndrome 65 2.548
182
MYL069 Myeloma, Multiple 77 2.543
183
c ATR087 Atrial Standstill 1 74 2.508
184
VRC005 Varicose Veins 60 2.506
185
SYN036 Syncope 45 2.506
186
BRN004 Brain Edema 54 2.505
187
STM007 Stomatitis 54 2.500
188
INT066 Interstitial Lung Disease 60 2.486
189
c HYP595 Hypertension, Essential 85 2.477
190
RST023 Resting Heart Rate, Variation in 40 2.474
191
P HYP055 Hypoplastic Left Heart Syndrome 65 2.474
192
ALG001 Algoneurodystrophy 38 2.463
193
ATX019 Ataxia with Vitamin E Deficiency 44 2.461
194
SNG003 Single Ventricular Heart 30 2.460
195
P MYS003 Myasthenia Gravis 68 2.460
196
AND005 Androgen Insensitivity Syndrome, Mild 21 2.438
197
P MTR003 Mitral Valve Stenosis 53 2.435
198
P ECL001 Eclampsia 52 2.429
199
P PTS002 Ptosis 52 2.424
200
ADL002 Adult Syndrome 70 2.405
201
APP008 Appendicitis 62 2.402
202
DWN001 Down Syndrome 70 2.389
203
P CHN012 Chondrosarcoma 57 2.387
204
SQM013 Squamous Cell Carcinoma, Head and Neck 73 2.385
205
ASP004 Asphyxia Neonatorum 50 2.363
206
P ESP024 Esophagitis 60 2.359
207
P ART022 Arthritis 71 2.356
208
SPN186 Spinal Cord Injury 61 2.353
209
ASP007 Aspiration Pneumonia 49 2.353
210
P ALZ034 Alzheimer Disease 87 2.345
211
P ATR010 Atrial Heart Septal Defect 58 2.311
212
P HYD006 Hydrocephalus 61 2.311
213
P URT039 Urticaria 58 2.311
214
P ALC033 Alcohol Use Disorder 61 2.307
215
INT146 Intervertebral Disc Disease 63 2.304
216
DFC004 Deficiency Anemia 74 2.291
217
P ESS003 Essential Thrombocythemia 69 2.280
218
BNN005 Bunion 31 2.267
219
P HPT021 Hepatitis 69 2.261
220
P HPT023 Hepatocellular Carcinoma 96 2.260
221
CRH001 Crohn's Disease 80 2.243
222
P MSC005 Muscular Dystrophy 67 2.235
223
CRB037 Cerebral Palsy 67 2.235
224
P HYP076 Hyperthyroidism 53 2.223
225
CRD223 Cardiac Arrhythmia 63 2.220
226
P PRK057 Parkinson Disease, Late-Onset 80 2.218
227
ACQ007 Acquired Immunodeficiency Syndrome 59 2.218
228
ACT084 Acute Stress Disorder 54 2.210
229
END057 Endometrial Cancer 72 2.210
230
SCK003 Sickle Cell Anemia 74 2.173
231
RSP019 Respiratory Distress Syndrome in Premature Infants 52 2.167
232
NWB001 Newborn Respiratory Distress Syndrome 56 2.167
233
RTN017 Retinal Detachment 60 2.160
234
P MYM013 Moyamoya Disease 1 59 2.154
235
P INF037 Inflammatory Bowel Disease 53 2.152
236
P INF032 Infertility 57 2.146
237
TNS005 Tonsillitis 57 2.140
238
APH002 Aphasia 56 2.129
239
P MTR012 Mitral Valve Disease 57 2.129
240
P GLL022 Guillain-Barre Syndrome 60 2.129
241
INT030 Intracranial Aneurysm 55 2.128
242
ANG054 Angina Pectoris 66 2.111
243
HYP005 Hypokalemia 55 2.107
244
PRS047 Prostatitis 58 2.101
245
P PRS040 Prostate Cancer 95 2.090
246
c CHR684 Chronic Kidney Disease 69 2.083
247
GRG001 Greig Cephalopolysyndactyly Syndrome 64 2.080
248
BRN038 Bronchial Disease 51 2.078
249
DRM006 Dermatitis 62 2.074
250
HRP004 Herpes Zoster 61 2.074
251
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 2.070
252
NRN005 Neuronal Ceroid-Lipofuscinoses 61 2.069
253
CVD001 Covid-19 57 2.069
254
DNT012 Dental Caries 53 2.069
255
c CNT035 Central Nervous System Disease 54 2.069
256
P TMP001 Temporal Lobe Epilepsy 49 2.068
257
ANT039 Antisynthetase Syndrome 55 2.050
258
BCT022 Bacterial Infectious Disease 56 2.029
259
DRG024 Drug Allergy 40 2.029
260
CHL014 Cholera 62 2.029
261
P RHN004 Rhinitis 57 2.029
262
P LKM062 Leukemia, Acute Lymphoblastic 69 2.023
263
PRP027 Peripheral Vascular Disease 71 2.010
264
PRS045 Prostatic Hypertrophy 53 2.005
265
P BLD134 Bladder Cancer 79 2.004
266
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 2.000
267
P TRT019 Torticollis 47 1.998
268
CHN016 Cohen Syndrome 60 1.982
269
INT007 Intermediate Coronary Syndrome 54 1.977
270
P MTC133 Mitochondrial Myopathy 50 1.977
271
CNT047 Contact Dermatitis 57 1.976
272
P CMP008 Compartment Syndrome 50 1.976
273
P GLL020 Gallbladder Disease 56 1.956
274
P NSP012 Nasopharyngeal Carcinoma 61 1.944
275
RDN001 Reading Disorder 40 1.930
276
P URN019 Urinary Tract Infection 49 1.930
277
P SCL057 Scoliosis, Isolated 1 40 1.930
278
P CRC039 Coarctation of Aorta 46 1.924
279
PNM010 Pneumothorax, Primary Spontaneous 58 1.924
280
c ACT075 Acute Myocardial Infarction 56 1.924
281
INS024 Insulin-Like Growth Factor I 78 1.921
282
CYS001 Cystic Fibrosis 78 1.921
283
SCN049 Second-Degree Atrioventricular Block 33 1.921
284
PRL008 Paralytic Ileus 45 1.921
285
PLY001 Polycythemia Vera 69 1.906
286
P PLY018 Polycythemia 56 1.906
287
PRS129 Prostatic Hyperplasia, Benign 49 1.905
288
INS001 Insulinoma 59 1.905
289
PRS021 Prostatic Adenoma 43 1.905
290
P CRV039 Cervicitis 52 1.899
291
CCN009 Cocaine Intoxication 30 1.892
292
CRD137 Cardiogenic Shock 56 1.892
293
P ART018 Aortic Valve Insufficiency 52 1.880
294
PST092 Posttransplant Acute Limbic Encephalitis 28 1.880
295
MTC004 Mitochondrial Encephalomyopathy 42 1.863
296
INF118 Inflammatory Myopathy with Abundant Macrophages 27 1.863
297
ATN005 Autonomic Dysfunction 46 1.863
298
MST024 Mastocytosis, Cutaneous 67 1.836
299
BRS051 Breast Disease 58 1.836
300
P FNG006 Feingold Syndrome 1 62 1.835
301
HYP056 Hypoglycemia 65 1.830
302
CHL067 Cholecystitis 60 1.825
303
c PRM093 Premature Ovarian Failure 7 48 1.810
304
P BCL017 B-Cell Lymphoma 59 1.803
305
ALL010 Allergic Contact Dermatitis 56 1.803
306
LYM027 Lymphopenia 56 1.803
307
P END033 Endocarditis 58 1.803
308
HYP264 Hypertonia 36 1.803
309
PRP016 Paraplegia 52 1.793
310
GST092 Gastroesophageal Reflux 61 1.778
311
c ACT134 Acute Liver Failure 59 1.777
312
P MYL006 Myeloid Leukemia 61 1.777
313
P THR014 Thrombocytopenia 66 1.777
314
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 1.777
315
SPN041 Spinal Cord Disease 55 1.777
316
MRP001 Morphine Dependence 42 1.763
317
ART074 Aortic Dissection 53 1.753
318
c FNC043 Fanconi Anemia, Complementation Group E 62 1.753
319
RNL114 Renal Cell Carcinoma, Nonpapillary 80 1.738
320
CHL079 Children's Interstitial Lung Disease 26 1.738
321
MYL009 Myelodysplastic Syndrome 67 1.736
322
GST050 Gastrointestinal System Disease 55 1.736
323
SCR035 Sacral Agenesis with Vertebral Anomalies 38 1.730
324
MSC157 Muscular Dystrophy, Duchenne Type 79 1.722
325
P DYS154 Dystonia 64 1.722
326
CRB004 Cerebral Artery Occlusion 45 1.722
327
CMP006 Complex Partial Epilepsy 36 1.722
328
FCL014 Focal Epilepsy 53 1.722
329
IRR003 Irritant Dermatitis 47 1.722
330
STT001 Status Epilepticus 59 1.722
331
NRT001 Neurotic Disorder 56 1.718
332
P OST002 Osteoporosis 76 1.670
333
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.670
334
MDD018 Middle East Respiratory Syndrome 44 1.670
335
STT002 Status Asthmaticus 49 1.670
336
c VSC019 Vesicoureteral Reflux 1 57 1.664
337
HPT004 Hepatic Coma 43 1.664
338
P LNG064 Lung Cancer Susceptibility 3 70 1.664
339
HPT019 Hepatic Encephalopathy 59 1.664
340
P PRP029 Porphyria 60 1.664
341
ANK001 Ankylosis 51 1.664
342
c MCL062 Mucolipidosis Ii Alpha/beta 68 1.644
343
P LYM118 Lymphoma 67 1.644
344
SPR126 Superior Semicircular Canal Dehiscence 41 1.644
345
P LRY019 Laryngitis 53 1.644
346
c HMG029 Hemoglobin Se Disease 40 1.644
347
LYM019 Lymphosarcoma 46 1.644
348
DSM003 Desmoid Disease, Hereditary 48 1.642
349
HMN044 Human Immunodeficiency Virus Type 1 78 1.617
350
ACH005 Achalasia 55 1.617
351
P ART023 Arthropathy 61 1.617
352
PRT013 Portal Hypertension 59 1.617
353
P BLD124 Bleeding Disorder, Platelet-Type, 11 67 1.608
354
c PRS136 Prostate Cancer, Hereditary, 6 33 1.608
355
c HYP724 Hyperlipoproteinemia, Type Iii 67 1.608
356
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 1.608
357
c PRS130 Prostate Cancer, Hereditary, 8 32 1.608
358
HYP458 Hyper Ige Syndrome 60 1.608
359
TWN001 Twin-to-Twin Transfusion Syndrome 46 1.603
360
P PRK039 Parkinsonism 55 1.603
361
PLM032 Pulmonary Blastoma 47 1.603
362
EMB002 Embryoma 37 1.603
363
P HYP077 Hypertrichosis 46 1.603
364
P FBR017 Fibrosarcoma 56 1.603
365
P BRS044 Breast Adenocarcinoma 58 1.603
366
MTS001 Mutism 44 1.603
367
NRL004 Neuroleptic Malignant Syndrome 52 1.603
368
MDD011 Mood Disorder 62 1.603
369
ORL011 Oral Cancer 60 1.603
370
ANS021 Anisocoria 25 1.597
371
P RST001 Restless Legs Syndrome 52 1.597
372
GLL048 Glial Tumor 52 1.597
373
GLM045 Glioma 63 1.597
374
P DMN002 Dementia 66 1.596
375
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 1.586
376
P ART005 Arteriovenous Malformation 65 1.586
377
P MYT002 Myotonic Dystrophy 51 1.586
378
ADN018 Adenoma 59 1.570
379
c SML038 Small Cell Cancer of the Lung 69 1.559
380
P BLR006 Biliary Tract Disease 46 1.559
381
LMY002 Leiomyoma 51 1.554
382
ALL003 Allergic Rhinitis 67 1.539
383
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 1.539
384
PLC008 Placenta Disease 49 1.539
385
MYC005 Myocardial Stunning 46 1.539
386
BRN056 Bronchopulmonary Dysplasia 56 1.539
387
P MJR001 Major Depressive Disorder 68 1.536
388
c THR090 Thrombocythemia 1 50 1.532
389
P ANP001 Anaplastic Large Cell Lymphoma 61 1.532
390
SPL004 Splenic Marginal Zone Lymphoma 50 1.532
391
CHR563 Chronic Eosinophilic Leukemia 48 1.532
392
MYL005 Myelofibrosis 71 1.532
393
CHR286 Chronic Neutrophilic Leukemia 43 1.532
394
P CHR285 Chronic Myelomonocytic Leukemia 60 1.532
395
EXT010 Extramedullary Plasmacytoma 46 1.532
396
MNC006 Monoclonal Gammopathy of Uncertain Significance 47 1.532
397
INT054 Intraocular Lymphoma 48 1.532
398
PRL017 Prolymphocytic Leukemia 47 1.532
399
c PRM012 Primary Polycythemia 58 1.532
400
RFR002 Refractory Hairy Cell Leukemia 34 1.532
401
c ALM001 Al Amyloidosis 54 1.532
402
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 1.532
403
PST046 Post-Transplant Lymphoproliferative Disease 53 1.532
404
P DRR001 Diarrhea 55 1.517
405
IRR002 Irritable Bowel Syndrome 65 1.517
406
EPT021 Epithelial Recurrent Erosion Dystrophy 46 1.514
407
ENT001 Enterocele 42 1.514
408
PRT036 Peritonitis 65 1.512
409
c TYP009 Type 2 Diabetes Mellitus 92 1.473
410
DFF031 Diffuse Alveolar Hemorrhage 31 1.471
411
INF034 Infective Endocarditis 54 1.471
412
PRP083 Porphyria, Acute Intermittent 65 1.471
413
P HML002 Hemolytic Anemia 62 1.471
414
P VNS003 Venous Insufficiency 55 1.471
415
P HYP086 Hypothyroidism 69 1.471
416
ESP002 Esophageal Varix 51 1.471
417
P PNM007 Pneumonia 67 1.471
418
MBT001 Mobitz Type Ii Atrioventricular Block 34 1.471
419
ACT017 Acute Chest Syndrome 50 1.471
420
P RHM011 Rheumatoid Arthritis 82 1.462
421
c PNC108 Pancreatitis, Hereditary 69 1.462
422
P CRP001 Carpal Tunnel Syndrome 66 1.462
423
URN010 Urinary Tract Obstruction 55 1.462
424
P HMR005 Hemorrhoid 49 1.436
425
MYF001 Myofibroma 42 1.436
426
LYM014 Lymphangitis 38 1.429
427
c MCL013 Mucolipidosis Iv 65 1.403
428
GLS018 Glass Syndrome 61 1.403
429
MRG013 Mirage Syndrome 44 1.403
430
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 1.403
431
FLL027 Fallopian Tube Carcinoma 67 1.403
432
END086 End Stage Renal Disease 52 1.399
433
P THL005 Thalassemia 56 1.397
434
c BTT014 Beta-Thalassemia 72 1.397
435
MYX013 Myxofibrosarcoma 44 1.397
436
URL001 Urolithiasis 46 1.397
437
P ORT004 Orthostatic Intolerance 63 1.397
438
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 1.397
439
P VND001 Vein Disease 42 1.397
440
PRV004 Periventricular Leukomalacia 52 1.397
441
BLR008 Bilirubin Metabolic Disorder 57 1.397
442
P MLN008 Melanoma 76 1.397
443
c RNG019 Ring Chromosome 3 19 1.397
444
P PLM064 Pulmonary Sequestration 22 1.397
445
ALC007 Alcohol Dependence 66 1.387
446
P OTF004 Otofaciocervical Syndrome 1 41 1.387
447
PST021 Postpartum Depression 50 1.355
448
STR067 Stroke, Ischemic 80 1.355
449
DVR002 Diverticulitis 46 1.355
450
CRN030 Coronary Stenosis 50 1.348
451
c ACT071 Acute Kidney Failure 60 1.348
452
c HPT003 Hepatitis a 63 1.345
453
CTS005 Catastrophic Antiphospholipid Syndrome 43 1.345
454
CRY008 Cryopyrin-Associated Periodic Syndrome 48 1.345
455
P AST005 Asthma 76 1.340
456
c ART101 Aortic Valve Disease 2 66 1.328
457
NRN002 Neuronitis 31 1.328
458
P KDN017 Kidney Cancer 61 1.328
459
CRB009 Cerebritis 43 1.322
460
c ART115 Aortic Valve Disease 1 74 1.318
461
LPM012 Lipomatosis, Multiple 60 1.318
462
CRY035 Cryptorchidism, Unilateral or Bilateral 58 1.318
463
c BRN108 Branchiootic Syndrome 1 62 1.318
464
TRG002 Trigeminal Neuralgia 61 1.318
465
CHL065 Cholangiocarcinoma 58 1.318
466
OST017 Osteomyelitis 63 1.318
467
PLM005 Pleomorphic Lipoma 40 1.318
468
HYD002 Hydronephrosis 58 1.318
469
INT079 Intrahepatic Cholangiocarcinoma 51 1.318
470
QDR001 Quadriplegia 50 1.318
471
c RNG015 Ring Chromosome 2 22 1.318
472
CYT018 Cytochrome P450 2d6 Variant 26 1.318
473
c PLM164 Pulmonary Hypertension, Primary, 1 76 1.295
474
ANL022 Anal Fistula 47 1.281
475
PPM002 Ppoma 28 1.258
476
c MST023 Mesothelioma, Malignant 56 1.258
477
DSM004 Desmoid Tumor 66 1.258
478
ZLL002 Zollinger-Ellison Syndrome 55 1.258
479
GST019 Gastrointestinal Stromal Tumor 78 1.258
480
ADN011 Adenoid Cystic Carcinoma 68 1.258
481
ADL045 Adult Ependymoblastoma 14 1.258
482
SMT003 Somatostatinoma 52 1.258
483
EXT025 Extragonadal Germ Cell Cancer 31 1.258
484
CNG029 Congenital Mesoblastic Nephroma 43 1.258
485
GST030 Gastrinoma 45 1.258
486
SML009 Small Intestine Adenocarcinoma 57 1.258
487
LCL004 Localized Osteosarcoma 34 1.258
488
ADL018 Adult Choroid Plexus Cancer 15 1.258
489
ADL023 Adult Medulloblastoma 42 1.258
490
KDN002 Kidney Rhabdoid Cancer 38 1.258
491
ADL033 Adult Papillary Meningioma 10 1.258
492
KDN007 Kidney Clear Cell Sarcoma 40 1.258
493
ADL054 Adult Brain Stem Glioma 29 1.258
494
SML008 Small Intestine Lymphoma 33 1.258
495
ADL008 Adult Oligodendroglioma 34 1.258
496
MLG023 Malignant Adult Ependymoma 15 1.258
497
MNN001 Meningeal Melanocytoma 38 1.258
498
ADL025 Adult Pineoblastoma 20 1.258
499
SML014 Small Intestine Leiomyosarcoma 31 1.258
500
APP010 Appendix Cancer 45 1.258
501
GLC036 Glucagonoma 46 1.258
502
c SVR005 Severe Pre-Eclampsia 50 1.246
503
P OVR046 Ovarian Cyst 46 1.240
504
URT001 Urethritis 53 1.234
505
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 1.229
506
MND002 Mandibuloacral Dysplasia with Type B Lipodystrophy 37 1.229
507
THR099 Third-Degree Atrioventricular Block 42 1.229
508
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 1.229
509
P HRP006 Herpes Simplex 65 1.229
510
THR016 Thrombophlebitis 50 1.229
511
CHL061 Childhood Leukemia 47 1.229
512
P PLM006 Pulmonary Alveolar Proteinosis 53 1.229
513
CHN011 Chondromalacia 37 1.229
514
ATN004 Autonomic Neuropathy 42 1.229
515
PLM011 Plummer's Disease 34 1.229
516
P LMY004 Leiomyosarcoma 62 1.229
517
P NRF002 Neurofibromatosis 57 1.229
518
P MYC008 Myocarditis 59 1.229
519
ALP103 Alpha-1-Antitrypsin Deficiency 68 1.209
520
GLC003 Glucose Intolerance 54 1.209
521
P OPT006 Optic Nerve Disease 58 1.209
522
PLR022 Pleural Disease 45 1.209
523
END040 Endogenous Depression 55 1.189
524
LPT006 Leptin Receptor Deficiency 50 1.184
525
CRN019 Coronary Artery Vasospasm 47 1.182
526
P OBS001 Obstructive Jaundice 48 1.182
527
P SCK002 Sick Sinus Syndrome 55 1.182
528
P BRN022 Bronchiectasis 60 1.166
529
P MTC069 Mitochondrial Disorders 57 1.166
530
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 1.129
531
PRP007 Priapism 47 1.129
532
HMG002 Hemoglobinuria 50 1.129
533
SKN016 Skin Disease 63 1.129
534
SPR007 Superior Mesenteric Artery Syndrome 37 1.129
535
P PLM036 Pulmonary Fibrosis 66 1.129
536
P ENT005 Entropion 34 1.129
537
ALC009 Alcoholic Liver Cirrhosis 54 1.129
538
P NRN021 Neuronal Ceroid Lipofuscinosis 65 1.129
539
THR004 Thrombocytosis 53 1.129
540
HYP006 Hypertensive Heart Disease 49 1.129
541
DCB001 Decubitus Ulcer 62 1.129
542
SYS003 Systolic Heart Failure 49 1.129
543
c SPN225 Spondyloarthropathy 1 70 1.121
544
KRN002 Kearns-Sayre Syndrome 63 1.121
545
PLR007 Pleural Empyema 51 1.121
546
SPN051 Spondylitis 51 1.121
547
TRC005 Tracheal Stenosis 43 1.121
548
P HYP061 Hypertrophic Cardiomyopathy 69 1.121
549
INF009 Inflammatory Spondylopathy 30 1.121
550
P END044 Endometriosis 62 1.121
551
LYM040 Lymphoblastic Lymphoma 53 1.121
552
EPD005 Epidural Abscess 31 1.121
553
MTR002 Mitral Valve Insufficiency 52 1.121
554
P URF003 Urofacial Syndrome 1 56 1.089
555
ACR008 Acrocallosal Syndrome 70 1.089
556
AYM001 Ayme-Gripp Syndrome 56 1.089
557
P LYM033 Lymphoproliferative Syndrome 59 1.089
558
P MCR129 Microvascular Complications of Diabetes 1 68 1.089
559
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 38 1.089
560
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 55 1.089
561
MNN028 Mononeuropathy of the Median Nerve, Mild 46 1.089
562
ACH015 Achalasia, Familial Esophageal 42 1.089
563
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 70 1.089
564
LWR018 Lower Urinary Tract Obstruction, Congenital 39 1.089
565
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 35 1.089
566
BNM001 Bone Marrow Cancer 46 1.089
567
MYL075 Myelodysplastic/myeloproliferative Neoplasm 51 1.089
568
P MST002 Mast-Cell Leukemia 50 1.089
569
P PRS038 Personality Disorder 65 1.089
570
BNG006 Benign Familial Neonatal Epilepsy 55 1.089
571
CNT033 Central Nervous System Cancer 47 1.089
572
P THY032 Thyroiditis 57 1.089
573
MYF002 Myofascial Pain Syndrome 46 1.089
574
HMT002 Hematologic Cancer 61 1.089
575
NSP002 Nasopharyngitis 45 1.089
576
THY122 Thyroid Gland Cancer 59 1.089
577
MYL031 Myeloproliferative Neoplasm 66 1.089
578
PLS009 Plasma Cell Neoplasm 64 1.089
579
P NRV006 Nervous System Cancer 48 1.089
580
DBT002 Diabetic Autonomic Neuropathy 41 1.089
581
RSP006 Respiratory System Disease 51 1.089
582
P BNG026 Benign Neonatal Seizures 49 1.089
583
URN009 Urinary System Disease 47 1.089
584
MGS001 Megaesophagus 44 1.089
585
CYS021 Cystic Adenomatoid Malformation of Lung 32 1.089
586
SPN354 Spinal Arachnoiditis 36 1.078
587
ARC002 Arachnoiditis 50 1.078
588
CRT013 Carotid Stenosis 51 1.078
589
HLL004 Hellp Syndrome 53 1.078
590
c PRG042 Progressive Familial Heart Block, Type Ia 66 1.057
591
c HPT073 Hepatitis C Virus 71 1.057
592
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 43 1.057
593
SPR004 Supravalvular Aortic Stenosis 57 1.057
594
THY029 Thyroid Carcinoma 51 1.057
595
c HPT001 Hepatitis C 62 1.057
596
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.057
597
MCR011 Microinvasive Gastric Cancer 41 1.057
598
P HYP069 Hyperparathyroidism 62 1.057
599
P PLY019 Polyneuropathy 52 1.057
600
c GLL024 Gallbladder Disease 1 52 1.054
601
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 1.054
602
P MGR001 Migraine Without Aura 49 1.054
603
CHL013 Cholecystolithiasis 37 1.054
604
SMT001 Somatization Disorder 50 1.054
605
CNG129 Congenital Torticollis 23 1.054
606
LNG031 Lung Benign Neoplasm 51 1.031
607
CLN045 Colonic Benign Neoplasm 48 1.031
608
PLM134 Pulmonary Fibrosis, Idiopathic 76 1.010
609
c DWL002 Dowling-Degos Disease 1 58 1.010
610
c SCL052 Scleroderma, Familial Progressive 61 1.010
611
P ALB003 Albinism-Deafness Syndrome 34 1.010
612
MCR037 Macroglossia 44 1.010
613
P PRG013 Paraganglioma 57 1.010
614
TND005 Tendinitis 54 1.010
615
HYP139 Hypotrichosis-Lymphedema-Telangiectasia Syndrome 45 1.010
616
MXL017 Maxillary Cancer 30 1.010
617
P ERY008 Erythromelalgia 50 1.010
618
ULC004 Ulcerative Colitis 74 1.010
619
c FML191 Familial Long Qt Syndrome 55 1.010
620
SHW001 Shwartzman Phenomenon 36 1.010
621
c ESS001 Essential Tremor 57 1.010
622
P MTR014 Motor Neuron Disease 65 1.010
623
P GLM007 Glomerulonephritis 60 1.010
624
NRF007 Neurofibroma 64 1.010
625
TNP004 Tn Polyagglutination Syndrome 42 0.989
626
P MLT020 Multiple Sclerosis 79 0.989
627
MYL020 Myelomeningocele 51 0.989
628
ENT011 Enterocolitis 55 0.989
629
BTT016 Batten-Turner Congenital Myopathy 53 0.989
630
P MVM001 Movement Disease 61 0.989
631
P LCT001 Lactic Acidosis 51 0.989
632
PPT005 Peptic Ulcer Disease 58 0.989
633
VRC001 Varicocele 48 0.989
634
LWC001 Low Compliance Bladder 45 0.989
635
SPN020 Spondylosis 46 0.989
636
GLC009 Glucosephosphate Dehydrogenase Deficiency 53 0.989
637
DSS009 Disseminated Intravascular Coagulation 57 0.989
638
HYP080 Hypogonadism 50 0.989
639
PRN019 Perinatal Necrotizing Enterocolitis 60 0.989
640
PRP080 Peripheral Artery Disease 54 0.977
641
c PNC106 Pancreatic Agenesis 1 51 0.977
642
MNN043 Meningioma, Familial 79 0.977
643
SCR001 Secretory Meningioma 40 0.977
644
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.977
645
PNC034 Pancreas Disease 50 0.977
646
SPN021 Spinal Meningioma 50 0.977
647
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 49 0.937
648
RSP007 Respiratory Distress Syndrome, Infant 40 0.937
649
GST009 Gastroschisis 53 0.916
650
MRF001 Marfan Syndrome 76 0.916
651
WLL001 Williams-Beuren Syndrome 61 0.916
652
ATS010 Autosomal Recessive Disease 42 0.916
653
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.916
654
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.916
655
P MSC003 Muscular Atrophy 52 0.916
656
DYS011 Dyskinesia of Esophagus 40 0.916
657
P MST009 Mastocytosis 64 0.916
658
TRC022 Tricuspid Valve Insufficiency 47 0.916
659
P INT070 Intestinal Obstruction 57 0.916
660
PNC001 Pancytopenia 53 0.916
661
P ADN016 Adenocarcinoma 63 0.916
662
P MYG005 Myoglobinuria 40 0.916
663
TTH004 Tethered Spinal Cord Syndrome 41 0.916
664
P MCR010 Microcephaly 60 0.916
665
CRD001 Cardiac Tamponade 43 0.916
666
c PRM005 Primary Hyperparathyroidism 59 0.916
667
P ART021 Arteriosclerosis 54 0.916
668
RGH001 Right Bundle Branch Block 47 0.916
669
ABD010 Abdominal Wall Defect 39 0.916
670
DBL004 Double Discordia 20 0.916
671
MTC005 Mitochondrial Metabolism Disease 45 0.859
672
THR024 Thrombosis 56 0.859
673
P SLP005 Sleep Disorder 61 0.859
674
DWR001 Dwarfism 44 0.859
675
LWF001 Low-Flow Priapism 16 0.856
676
FRG010 Fragile X Tremor/ataxia Syndrome 44 0.856
677
P BCK002 Beckwith-Wiedemann Syndrome 62 0.856
678
PRL045 Proline-Negative Auxotroph of Hamster, Complementation of 16 0.856
679
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 44 0.856
680
HPT022 Hepatoblastoma 54 0.856
681
TRN015 Transient Cerebral Ischemia 63 0.856
682
BLR001 Biliary Atresia 55 0.856
683
P PRL003 Proliferative Glomerulonephritis 43 0.856
684
KRK001 Krukenberg Carcinoma 39 0.856
685
CRD016 Cardiac Rupture 34 0.856
686
GGN002 Gigantism 33 0.856
687
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.836
688
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.836
689
STF001 Stiff-Person Syndrome 58 0.836
690
ASP008 Aspiration Pneumonitis 42 0.836
691
P RHB003 Rhabdomyosarcoma 66 0.836
692
SBV001 Subvalvular Aortic Stenosis 30 0.836
693
P EPL164 Epilepsy 68 0.836
694
P CHR071 Charcot-Marie-Tooth Disease 64 0.836
695
PLC002 Plica Syndrome 35 0.836
696
P LTR001 Lateral Sclerosis 58 0.836
697
P HMN010 Hemangioma 62 0.836
698
FCL012 Facial Paralysis 49 0.836
699
TTH006 Tooth Disease 51 0.836
700
CDQ001 Cauda Equina Syndrome 37 0.836
701
SYN007 Synovitis 55 0.836
702
P TCD001 Tic Disorder 49 0.836
703
PTN001 Patent Foramen Ovale 62 0.836
704
MLG086 Malignant Hyperthermia Susceptibility 39 0.836
705
PTT037 Pituitary Tumors 44 0.836
706
P CHR342 Chiari Malformation 41 0.836
707
ETN001 Eating Disorder 59 0.836
708
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.826
709
DFN270 Deafness, Dystonia, and Cerebral Hypomyelination 41 0.826
710
P DYS193 Dystonia 11, Myoclonic 55 0.826
711
P CNR004 Cone-Rod Dystrophy 2 74 0.826
712
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 0.826
713
BHR001 Behr Syndrome 51 0.826
714
P PRC031 Preeclampsia/eclampsia 1 43 0.826
715
MCN017 Meconium Ileus 53 0.826
716
DVR001 Diverticulitis of Colon 24 0.826
717
CNT097 Central Hypoventilation Syndrome, Congenital 70 0.782
718
CNG506 Congenital Amyoplasia 27 0.748
719
SPS019 Spastic Paraparesis 38 0.748
720
THY128 Thyroid Tumor 35 0.748
721
SVN002 Sveinsson Chorioretinal Atrophy 45 0.748
722
SPP011 Suppression of Tumorigenicity 12 61 0.748
723
BRT054 Brittle Bone Disorder 74 0.748
724
ATM095 Autoimmune Disease 61 0.748
725
c THR092 Thrombophilia Due to Thrombin Defect 74 0.748
726
PLN026 Pilonidal Sinus 35 0.748
727
P BRG001 Brugada Syndrome 69 0.748
728
TRC010 Trichotillomania 50 0.748
729
SXL003 Sexual Disorder 49 0.748
730
RHM028 Rheumatic Heart Disease 56 0.748
731
SPN392 Spondylosis, Cervical 30 0.748
732
SPN019 Spondylolisthesis 52 0.748
733
OST159 Osteogenic Sarcoma 66 0.748
734
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 0.748
735
P PTT006 Pituitary Adenoma 55 0.748
736
SYS004 Systemic Mastocytosis 63 0.748
737
NRM005 Neuromuscular Disease 63 0.748
738
P OTS001 Otosclerosis 49 0.748
739
P NTR004 Neutropenia 63 0.748
740
DSC005 Descending Colon Cancer 33 0.748
741
BRN014 Bronchopneumonia 53 0.748
742
ACR007 Acromegaly 70 0.748
743
P MTH007 Methemoglobinemia 46 0.748
744
HMP005 Hemiplegia 54 0.748
745
MCN007 Meconium Aspiration Syndrome 53 0.748
746
ART008 Arteriosclerosis Obliterans 40 0.748
747
STR015 Stereotypic Movement Disorder 32 0.748
748
GST037 Gastroparesis 52 0.748
749
P EHL001 Ehlers-Danlos Syndrome 58 0.748
750
MYT011 Myotonia 39 0.748
751
CHR178 Chromosomal Triplication 34 0.748
752
CRC006 Carcinoid Syndrome 55 0.748
753
c MCL046 Mucolipidosis Iii Alpha/beta 60 0.738
754
P PRS049 Persistent Mullerian Duct Syndrome 52 0.738
755
ACR041 Acromelic Frontonasal Dysostosis 53 0.738
756
c LKM060 Leukemia, Acute Lymphoblastic 3 49 0.738
757
PRS128 Persistent Mullerian Duct Syndrome, Types I and Ii 43 0.738
758
ORB013 Orbital Disease 42 0.738
759
BRN028 Brain Cancer 74 0.738
760
PSY004 Psychotic Disorder 66 0.738
761
PHR003 Pharyngitis 58 0.738
762
NRD100 Neurodevelopmental, Jaw, Eye, and Digital Syndrome 49 0.704
763
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 46 0.704
764
LMB062 Limb Ischemia 55 0.704
765
PNC085 Penicillin Allergy 43 0.704
766
P ISL078 Isolated Ectopia Lentis 58 0.704
767
MTH009 Mouth Disease 57 0.704
768
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.704
769
PYL006 Pyloric Stenosis 48 0.704
770
P HYP009 Hypertrophic Pyloric Stenosis 41 0.704
771
IRN002 Iron Metabolism Disease 57 0.704
772
ATH013 Atherosclerosis Susceptibility 63 0.681
773
c EHL080 Ehlers-Danlos Syndrome, Musculocontractural Type, 1 52 0.681
774
c BLD140 Blood Group, I System 46 0.681
775
FML037 Female Breast Cancer 51 0.681
776
c FML001 Familial Atrial Fibrillation 65 0.681
777
KHL003 Kohlschutter-Tonz Syndrome 59 0.681
778
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 64 0.681
779
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 40 0.681
780
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 29 0.681
781
P NJM001 Nijmegen Breakage Syndrome 76 0.681
782
3MC001 3mc Syndrome 2 35 0.681
783
NRR001 Neuroretinitis 42 0.681
784
AGG012 Aggressive Nk-Cell Leukemia 46 0.681
785
P MLG074 Malignant Mesenchymoma 40 0.681
786
RTN023 Retinitis 46 0.681
787
CLF049 Cleft Lip and Alveolus 32 0.681
788
CRV025 Cervical Incompetence 35 0.681
789
P BLD036 Bile Duct Disease 44 0.681
790
FNC005 Functional Colonic Disease 21 0.681
791
SPN035 Spindle Cell Sarcoma 54 0.681
792
P MGR003 Migraine with Aura 52 0.681
793
CRT017 Cartilage Disease 53 0.681
794
PLM022 Pulmonary Valve Insufficiency 45 0.681
795
SRC014 Sarcoma 65 0.681
796
PRD004 Prediabetes Syndrome 52 0.681
797
PTL003 Patellar Tendinitis 29 0.681
798
CLN019 Colonic Disease 47 0.681
799
P INT068 Intestinal Disease 53 0.681
800
3MC003 3mc Syndrome 49 0.681
801
INT053 Intracranial Vasospasm 36 0.681
803
SFT003 Soft Tissue Sarcoma 57 0.681
804
P ATS364 Autism 69 0.647
805
UNV002 Univentricular Heart 26 0.647
806
ORN008 Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to 62 0.647
807
P RTT002 Rett Syndrome 79 0.647
808
MSC152 Muscular Dystrophy, Becker Type 69 0.647
809
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 50 0.647
810
HYP540 Hypertension, Diastolic 37 0.647
811
c CRD147 Cardiomyopathy, Familial Hypertrophic, 20 55 0.647
812
HMN047 Human Cytomegalovirus Infection 57 0.647
813
UMB002 Umbilical Hernia 47 0.647
814
P OMP004 Omphalocele 48 0.647
815
BNR002 Bone Resorption Disease 47 0.647
816
c CRD065 Cardiomyopathy, Familial Hypertrophic, 2 47 0.647
817
P PRD006 Prader-Willi Syndrome 61 0.647
818
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.647
819
HRN029 Hearing Loss, Noise-Induced 37 0.647
820
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 0.647
821
P SRC025 Sarcoidosis 1 71 0.647
822
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.647
823
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.647
824
P NNN008 Noonan Syndrome 1 77 0.647
825
P VNW001 Von Willebrand's Disease 65 0.647
826
TNG007 Tongue Carcinoma 52 0.647
827
VST001 Vestibular Neuronitis 33 0.647
828
LTX001 Latex Allergy 42 0.647
829
P NRC002 Narcolepsy 56 0.647
830
SPN185 Spinal Cord Infarction 28 0.647
831
P HYP098 Hypereosinophilic Syndrome 66 0.647
832
PRC013 Pericarditis 53 0.647
833
CLL003 Cellulitis 53 0.647
834
PLC005 Placental Insufficiency 56 0.647
835
P RST002 Restrictive Cardiomyopathy 54 0.647
836
PLX004 Plexopathy 29 0.647
837
PLM041 Pulmonary Valve Stenosis 50 0.647
838
BRC010 Brachial Plexus Lesion 34 0.647
839
PRP009 Peripartum Cardiomyopathy 55 0.647
840
P SNS001 Sensorineural Hearing Loss 59 0.647
841
SPP007 Suppression Amblyopia 38 0.647
842
AMB002 Amblyopia 50 0.647
843
P GRF003 Graft-Versus-Host Disease 71 0.647
844
CNR001 Coenurosis 26 0.647
845
P GRV001 Graves' Disease 55 0.647
846
GTR002 Goiter 53 0.647
847
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.647
848
CRD003 Cardiac Sarcoidosis 44 0.647
849
P DDN001 Duodenal Ulcer 53 0.647
850
P HMR003 Hemorrhagic Disease 59 0.647
851
GST033 Gestational Diabetes 61 0.647
852
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 57 0.647
853
P DMY001 Demyelinating Polyneuropathy 41 0.647
854
PRT029 Parathyroid Adenoma 51 0.647
855
P TRT010 Teratoma 51 0.647
856
PRP030 Purpura 54 0.647
857
P EPD016 Epidermolysis Bullosa 53 0.647
858
VST004 Vestibular Disease 40 0.647
859
PLC007 Placental Abruption 47 0.647
860
SBS004 Substance Dependence 47 0.647
861
P ENC004 Encephalitis 61 0.647
862
OPS006 Opsoclonus-Myoclonus Syndrome 48 0.647
863
c PSD047 Pseudo-Turner Syndrome 52 0.647
864
FNT004 Fainting 29 0.647
865
CNG134 Congenitally Corrected Transposition of the Great Arteries 38 0.647
866
ESN011 Eisenmenger Syndrome 47 0.647
867
HYP144 Hyperacusis 23 0.647
868
P KRB001 Krabbe Disease 69 0.529
869
c SCN052 Secondary Adrenal Insufficiency 36 0.529
870
ADR022 Adrenomyeloneuropathy 39 0.529
871
c INH030 Inherited Retinal Disorder 28 0.529
872
c ACQ047 Acquired Methemoglobinemia 30 0.529
873
WBR001 Weber Syndrome 38 0.529
874
c ACT150 Acute Adrenal Insufficiency 48 0.529
875
ATR048 Atrial Tachyarrhythmia with Short Pr Interval 25 0.529
876
SMT004 Smith-Lemli-Opitz Syndrome 70 0.529
877
c OPT051 Opitz Gbbb Syndrome, Type I 46 0.529
878
ADR007 Adrenoleukodystrophy 73 0.529
879
c THY107 Thymoma, Familial 42 0.529
880
CRD132 Cardiac Conduction Defect 60 0.529
881
TNG002 Tangier Disease 64 0.529
882
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.529
883
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 62 0.529
884
P MYS005 Myositis 56 0.529
885
OBS002 Obsessive-Compulsive Disorder 68 0.529
886
TRT017 Teratoma, Ovarian 28 0.529
887
PPL052 Papillomatosis, Confluent and Reticulated 34 0.529
888
c CRN139 Cornelia De Lange Syndrome 1 61 0.529
889
FCT001 Factor Viii Deficiency 60 0.529
890
SYR010 Syringomyelia, Noncommunicating Isolated 36 0.529
891
VNH007 Von Hippel-Lindau Syndrome 73 0.529
892
c CHR579 Chiari Malformation Type Ii 44 0.529
893
P DST002 Distal Arthrogryposis 65 0.529
894
P ERL057 Early Infantile Epileptic Encephalopathy 60 0.529
895
CHR005 Chorioamnionitis 50 0.529
896
c MJR022 Major Affective Disorder 8 38 0.529
897
c ACT249 Acute Asthma 40 0.529
898
MST019 Mastoiditis 41 0.529
899
SNT005 Sinoatrial Node Disease 47 0.529
900
END020 Endocardial Fibroelastosis 51 0.529
901
P BRN019 Bernard-Soulier Syndrome 61 0.529
902
IMM167 Immune Deficiency Disease 78 0.529
903
TRD006 Tardive Dyskinesia 53 0.529
904
c GRV008 Graves Disease 1 54 0.529
905
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.529
906
VRG001 Variegate Porphyria 56 0.529
907
PRG023 Progeroid Short Stature with Pigmented Nevi 32 0.529
908
GLY010 Glycine Encephalopathy 57 0.529
909
TRC062 Tricuspid Atresia 55 0.529
910
PRP001 Propionic Acidemia 65 0.529
911
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 0.529
912
c MJR024 Major Affective Disorder 9 41 0.529
913
c BRS111 Breast-Ovarian Cancer, Familial 2 53 0.529
914
PLY068 Polysubstance Abuse 41 0.529
915
c HMP029 Hemophilia a 68 0.529
916
CTR172 Citrullinemia, Classic 65 0.529
917
SCH038 Schopf-Schulz-Passarge Syndrome 51 0.529
918
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 54 0.529
919
MYX012 Myxoma, Intracardiac 30 0.529
920
DNT005 Dentatorubral-Pallidoluysian Atrophy 60 0.529
921
FBR011 Fibrodysplasia Ossificans Progressiva 67 0.529
922
P HYP726 Hypercalcemia, Infantile, 1 58 0.529
923
P HYP750 Hypertriglyceridemia, Familial 62 0.529
924
c EHL074 Ehlers-Danlos Syndrome, Classic Type, 2 43 0.529
925
THY111 Thyroid Carcinoma, Familial Medullary 67 0.529
926
PMP006 Pemphigus Vulgaris, Familial 58 0.529
927
P GLM040 Glioma Susceptibility 1 71 0.529
928
HRN026 Hernia, Hiatus 47 0.529
929
HRW001 Hair Whorl 35 0.529
930
ACH004 Achondroplasia 66 0.529
931
SCH036 Scheie Syndrome 73 0.529
932
P PRT026 Parotitis 42 0.529
933
RNL078 Renal Dysplasia 46 0.529
934
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.529
935
PNS018 Pain Sensitivity Quantitative Trait Locus 1 23 0.529
936
STS002 Situs Inversus 45 0.529
937
P PMP001 Pemphigus 55 0.529
938
P VSC011 Vasculitis 61 0.529
939
LRN003 Learning Disability 49 0.529
940
c BCT013 Bacterial Pneumonia 48 0.529
941
FND002 Fundus Dystrophy 55 0.529
942
P PLM034 Pulmonary Emphysema 58 0.529
943
P PLY017 Polyarteritis Nodosa 60 0.529
944
c PRG106 Progressive Muscular Dystrophy 32 0.529
945
P BRD002 Bardet-Biedl Syndrome 66 0.529
946
P BPL003 Bipolar Disorder 56 0.529
947
GNG008 Ganglioneuroblastoma 47 0.529
948
THY125 Thyroid Gland Medullary Carcinoma 48 0.529
949
BLD131 Bladder Urothelial Carcinoma 60 0.529
950
LDW001 Ludwig's Angina 25 0.529
951
ACT056 Acute Cor Pulmonale 38 0.529
952
P DRM010 Dermatomyositis 61 0.529
953
LFT001 Left Bundle Branch Hemiblock 47 0.529
954
P KLP003 Klippel-Feil Syndrome 47 0.529
955
END021 Endomyocardial Fibrosis 56 0.529
956
OLG003 Oligohydramnios 51 0.529
957
PCD001 Pica Disease 38 0.529
958
NRG002