Search results for Dexmedetomidine

681 hits were found for Dexmedetomidine

# Family MCID Name MIFTS Score
1
PNG002 Pain Agnosia 51 0.788
2
SBC016 Subacute Delirium 44 0.624
3
ANX010 Anxiety 73 0.319
4
ISC004 Ischemia 58 0.315
5
DPR016 Depression 63 0.301
6
MNT002 Mental Depression 58 0.300
7
48X005 48,xyyy 39 0.249
8
c PNS012 Paine Syndrome 61 0.237
9
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.235
10
CHL079 Children's Interstitial Lung Disease 26 0.234
11
c HYP595 Hypertension, Essential 84 0.228
12
P SLP006 Sleep Apnea 69 0.225
13
P HRT032 Heart Disease 75 0.219
14
P RSP003 Respiratory Failure 74 0.203
15
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.196
16
HYP266 Hypoxia 57 0.193
17
BRN071 Brain Injury 49 0.191
18
AMN003 Amnestic Disorder 54 0.186
19
WTH001 Withdrawal Disorder 48 0.168
20
APN008 Apnea, Obstructive Sleep 64 0.166
21
TRM010 Traumatic Brain Injury 51 0.166
22
P KDN018 Kidney Disease 72 0.164
23
P CHR345 Chronic Pain 44 0.164
24
P CNR004 Cone-Rod Dystrophy 2 73 0.162
25
CYT002 Cytokine Deficiency 42 0.162
26
P CTR002 Cataract 60 0.160
27
P TRN020 Turner Syndrome 67 0.158
28
c ACT071 Acute Kidney Failure 60 0.158
29
P SZR006 Seizure Disorder 56 0.158
30
ADL002 Adult Syndrome 70 0.156
31
P CRD119 Cardiac Arrest 67 0.156
32
TXC005 Toxic Shock Syndrome 62 0.156
33
c RHB024 Rhabdomyosarcoma 2 67 0.152
34
c FNC043 Fanconi Anemia, Complementation Group E 62 0.152
35
ATX019 Ataxia with Vitamin E Deficiency 42 0.147
36
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.142
37
TXC002 Toxic Encephalopathy 53 0.140
38
ING001 Inguinal Hernia 60 0.138
39
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.135
40
P ATR011 Atrial Fibrillation 66 0.133
41
LPP008 Lipoprotein Quantitative Trait Locus 62 0.133
42
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.130
43
P BRS047 Breast Cancer 97 0.127
44
P SCL018 Scoliosis 60 0.127
45
OCL069 Ocular Motor Apraxia 51 0.127
46
DWN001 Down Syndrome 70 0.125
47
P ENC018 Encephalopathy 61 0.125
48
ANR040 Aneurysm 59 0.125
49
HRT011 Heart Septal Defect 50 0.125
50
P EPL164 Epilepsy 71 0.122
51
P TTR001 Tetralogy of Fallot 70 0.122
52
P PLM037 Pulmonary Hypertension 67 0.122
53
P VSC007 Vascular Disease 63 0.122
54
SPN186 Spinal Cord Injury 60 0.122
55
VSL002 Visual Epilepsy 59 0.122
56
P STR020 Strabismus 55 0.119
57
MCH006 Mechanical Strabismus 42 0.119
58
P PRK057 Parkinson Disease, Late-Onset 78 0.116
59
c ATR087 Atrial Standstill 1 75 0.116
60
P ATS364 Autism 70 0.116
61
c PRC016 Pre-Eclampsia 63 0.116
62
DSS008 Disease of Mental Health 58 0.116
63
ATR057 Atrioventricular Block 55 0.116
64
INT075 Intracranial Hypertension 53 0.116
65
P PNM007 Pneumonia 68 0.113
66
P TRM003 Tremor 54 0.113
67
P LNG032 Lung Cancer 98 0.110
68
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.110
69
CNG034 Congestive Heart Failure 69 0.110
70
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.110
71
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.110
72
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.110
73
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.110
74
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.110
75
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.110
76
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.110
77
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.110
78
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.110
79
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.110
80
CRB039 Cerebrovascular Disease 67 0.107
81
PSY004 Psychotic Disorder 67 0.107
82
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.107
83
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.107
84
ILS001 Ileus 51 0.107
85
P ECL001 Eclampsia 50 0.107
86
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.107
87
P GST053 Gastric Cancer 83 0.104
88
P MYC007 Myocardial Infarction 70 0.104
89
P LVR013 Liver Disease 68 0.104
90
P CRN300 Coronary Heart Disease 1 63 0.104
91
BRN004 Brain Edema 56 0.104
92
P AGN002 Agnosia 55 0.104
93
CRB004 Cerebral Artery Occlusion 45 0.104
94
BRN028 Brain Cancer 74 0.101
95
HYP066 Hyperglycemia 61 0.101
96
P HDC001 Headache 57 0.101
97
HYP005 Hypokalemia 55 0.101
98
STR067 Stroke, Ischemic 81 0.097
99
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.097
100
ALL026 Allergic Hypersensitivity Disease 62 0.097
101
LNG099 Lung Disease 60 0.097
102
PLM010 Pulmonary Edema 54 0.097
103
RDN001 Reading Disorder 40 0.097
104
ENT001 Enterocele 39 0.097
105
P PHC003 Pheochromocytoma 71 0.094
106
P DMN002 Dementia 66 0.094
107
c FML001 Familial Atrial Fibrillation 65 0.094
108
P VNT002 Ventricular Septal Defect 60 0.094
109
PNM008 Pneumothorax 56 0.094
110
ART140 Arteries, Anomalies of 52 0.094
111
P HYP040 Hypospadias 51 0.094
112
END086 End Stage Renal Disease 51 0.094
113
ADR040 Adrenal Gland Pheochromocytoma 46 0.094
114
ESP021 Esophageal Cancer 90 0.090
115
KHL003 Kohlschutter-Tonz Syndrome 65 0.090
116
AYM001 Ayme-Gripp Syndrome 57 0.090
117
INT030 Intracranial Aneurysm 56 0.090
118
MCN017 Meconium Ileus 52 0.090
119
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.090
120
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.090
121
P CLR023 Colorectal Cancer 99 0.086
122
c THR092 Thrombophilia Due to Thrombin Defect 73 0.086
123
CRB037 Cerebral Palsy 69 0.086
124
P ART005 Arteriovenous Malformation 65 0.086
125
P ADL010 Adult Respiratory Distress Syndrome 65 0.086
126
CLF027 Cleft Palate, Isolated 64 0.086
127
MSC007 Muscle Hypertrophy 64 0.086
128
P ATR010 Atrial Heart Septal Defect 60 0.086
129
P SLP005 Sleep Disorder 59 0.086
130
P ALC033 Alcohol Use Disorder 58 0.086
131
SPN369 Spinal Disease 43 0.086
132
STT001 Status Epilepticus 60 0.082
133
SPN027 Spinal Stenosis 59 0.082
134
P EXN002 Exanthem 57 0.082
135
P CRD246 Cardiovascular System Disease 57 0.082
136
HRT012 Heart Valve Disease 53 0.082
137
CLF001 Cleft Lip 53 0.082
138
BKR002 Baker-Gordon Syndrome 49 0.082
139
ACT084 Acute Stress Disorder 47 0.082
140
CRD137 Cardiogenic Shock 47 0.082
141
P MYC033 Myoclonus 46 0.082
142
SCR035 Sacral Agenesis with Vertebral Anomalies 38 0.082
143
OST012 Osteoarthritis 78 0.078
144
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.078
145
c ATS007 Autism Spectrum Disorder 67 0.078
146
P MLG056 Malignant Hyperthermia 67 0.078
147
PRT037 Pertussis 65 0.078
148
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.078
149
P DBT009 Diabetes Mellitus 64 0.078
150
P BCL017 B-Cell Lymphoma 58 0.078
151
CNS004 Constipation 58 0.078
152
CRT013 Carotid Stenosis 50 0.078
153
MTB004 Metabolic Acidosis 50 0.078
154
47X002 47,xyy 49 0.078
155
GLL048 Glial Tumor 45 0.078
156
PTT037 Pituitary Tumors 44 0.078
157
c GZP005 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 44 0.078
158
CRB086 Cerebral Aneurysms 40 0.078
159
P PRC031 Preeclampsia/eclampsia 1 38 0.078
160
P HPT023 Hepatocellular Carcinoma 100 0.074
161
LPT014 Leptin Deficiency or Dysfunction 74 0.074
162
c CHR684 Chronic Kidney Disease 70 0.074
163
P ART022 Arthritis 69 0.074
164
ART016 Aortic Aneurysm 69 0.074
165
P GLM045 Glioma 63 0.074
166
PNM010 Pneumothorax, Primary Spontaneous 60 0.074
167
ORL011 Oral Cancer 60 0.074
168
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.074
169
TNS005 Tonsillitis 57 0.074
170
ACR041 Acromelic Frontonasal Dysostosis 52 0.074
171
P MSC003 Muscular Atrophy 52 0.074
172
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.074
173
ANT019 Anterograde Amnesia 38 0.074
174
P BLD134 Bladder Cancer 79 0.069
175
AST005 Asthma 76 0.069
176
P SCH015 Schizophrenia 74 0.069
177
P OCL013 Oculodentodigital Dysplasia 69 0.069
178
P HYP086 Hypothyroidism 69 0.069
179
P MSC005 Muscular Dystrophy 66 0.069
180
HYP056 Hypoglycemia 66 0.069
181
P NRV007 Nervous System Disease 66 0.069
182
TTN003 Tetanus 65 0.069
183
P DYS154 Dystonia 65 0.069
184
PPL049 Papillon-Lefevre Syndrome 65 0.069
185
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.069
186
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 64 0.069
187
P SPN046 Spinal Muscular Atrophy 62 0.069
188
P ART023 Arthropathy 62 0.069
189
DRM006 Dermatitis 61 0.069
190
RTN017 Retinal Detachment 61 0.069
191
CRD223 Cardiac Arrhythmia 60 0.069
192
P OPT006 Optic Nerve Disease 60 0.069
193
CMP010 Complex Regional Pain Syndrome 58 0.069
194
P BPL003 Bipolar Disorder 56 0.069
195
GST050 Gastrointestinal System Disease 56 0.069
196
LMB062 Limb Ischemia 55 0.069
197
PRP016 Paraplegia 52 0.069
198
P RCT021 Rectum Cancer 52 0.069
199
THY030 Thyroid Gland Disease 52 0.069
200
SPS003 Spastic Diplegia 51 0.069
201
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.069
202
CVD001 Covid-19 44 0.069
203
TRP009 Triple X Syndrome 42 0.069
204
GST020 Gastric Antral Vascular Ectasia 41 0.069
205
c MJR024 Major Affective Disorder 9 41 0.069
206
TRC005 Tracheal Stenosis 38 0.069
207
c MJR022 Major Affective Disorder 8 38 0.069
208
BNN005 Bunion 33 0.069
209
P PRS040 Prostate Cancer 97 0.064
210
MSC157 Muscular Dystrophy, Duchenne Type 72 0.064
211
DFC004 Deficiency Anemia 70 0.064
212
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.064
213
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.064
214
P PRS038 Personality Disorder 65 0.064
215
P MVM001 Movement Disease 63 0.064
216
c SVR001 Severe Acute Respiratory Syndrome 62 0.064
217
c ACT027 Acute Pancreatitis 60 0.064
218
PST028 Post-Traumatic Stress Disorder 58 0.064
219
P URT039 Urticaria 58 0.064
220
NWB001 Newborn Respiratory Distress Syndrome 58 0.064
221
c ACT075 Acute Myocardial Infarction 57 0.064
222
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.064
223
c ESS001 Essential Tremor 56 0.064
224
P NRP001 Neuropathy 56 0.064
225
SCH003 Schizophreniform Disorder 56 0.064
226
P DRR001 Diarrhea 55 0.064
227
P PTT006 Pituitary Adenoma 55 0.064
228
CLF004 Cleft Lip/palate 54 0.064
229
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 0.064
230
c SPN394 Spinal Muscular Atrophy, Type Iii 53 0.064
231
LMY002 Leiomyoma 52 0.064
232
BHR001 Behr Syndrome 51 0.064
233
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.064
234
P BLD051 Blood Coagulation Disease 46 0.064
235
c DRR009 Diarrhea 6 46 0.064
236
CRT015 Carotid Artery Occlusion 45 0.064
237
BCK006 Back Pain 42 0.064
238
HRW001 Hair Whorl 36 0.064
239
CHR178 Chromosomal Triplication 35 0.064
240
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 33 0.064
241
c PRS136 Prostate Cancer, Hereditary, 6 33 0.064
242
c PRS130 Prostate Cancer, Hereditary, 8 32 0.064
243
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.058
244
P OVR042 Ovarian Cancer 88 0.058
245
P ALZ034 Alzheimer Disease 88 0.058
246
P NRB001 Neuroblastoma 72 0.058
247
OTT002 Otitis Media 72 0.058
248
P LNG028 Long Qt Syndrome 66 0.058
249
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.058
250
P HYP055 Hypoplastic Left Heart Syndrome 63 0.058
251
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.058
252
c BRN108 Branchiootic Syndrome 1 62 0.058
253
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.058
254
VRC005 Varicose Veins 60 0.058
255
ETN001 Eating Disorder 60 0.058
256
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.058
257
THY122 Thyroid Gland Cancer 57 0.058
258
HMR039 Hemorrhage, Intracerebral 57 0.058
259
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 56 0.058
260
P SBS003 Substance Abuse 55 0.058
261
DBT010 Diabetic Neuropathy 54 0.058
262
PRS045 Prostatic Hypertrophy 53 0.058
263
BRN038 Bronchial Disease 53 0.058
264
c CNT035 Central Nervous System Disease 52 0.058
265
PRS030 Persistent Fetal Circulation Syndrome 52 0.058
266
PRS021 Prostatic Adenoma 51 0.058
267
SPN019 Spondylolisthesis 51 0.058
268
c INF145 Infantile Liver Failure Syndrome 1 50 0.058
269
DYS073 Dysphagia 50 0.058
270
PRS129 Prostatic Hyperplasia, Benign 49 0.058
271
ASP007 Aspiration Pneumonia 48 0.058
272
HYD005 Hydrocele 46 0.058
273
OPD001 Opioid Abuse 46 0.058
274
SPN040 Spinal Cancer 44 0.058
275
PLY068 Polysubstance Abuse 43 0.058
276
ORB013 Orbital Disease 42 0.058
277
c HYP543 Hypoplastic Left Heart Syndrome 1 40 0.058
278
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.058
279
LRY026 Laryngeal Cleft 27 0.058
280
P PNC035 Pancreatic Cancer 84 0.052
281
P GLM040 Glioma Susceptibility 1 81 0.052
282
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.052
283
CNT097 Central Hypoventilation Syndrome, Congenital 71 0.052
284
ALC007 Alcohol Dependence 66 0.052
285
ANG054 Angina Pectoris 66 0.052
286
P HYD006 Hydrocephalus 66 0.052
287
c ART101 Aortic Valve Disease 2 65 0.052
288
NRM005 Neuromuscular Disease 64 0.052
289
P ADN016 Adenocarcinoma 64 0.052
290
NTR005 Nutritional Deficiency Disease 62 0.052
291
APP008 Appendicitis 61 0.052
292
P KDN017 Kidney Cancer 60 0.052
293
HPT019 Hepatic Encephalopathy 60 0.052
294
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.052
295
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.052
296
P END033 Endocarditis 57 0.052
297
P PRV006 Pervasive Developmental Disorder 57 0.052
298
P MLT074 Multiple Endocrine Neoplasia 56 0.052
299
NRL004 Neuroleptic Malignant Syndrome 56 0.052
300
P PLY019 Polyneuropathy 56 0.052
301
P ATR001 Atrioventricular Septal Defect 55 0.052
302
P DYS193 Dystonia 11, Myoclonic 55 0.052
303
P DBT005 Diabetes Insipidus 55 0.052
304
INF034 Infective Endocarditis 53 0.052
305
NRT001 Neurotic Disorder 53 0.052
306
P LCT001 Lactic Acidosis 51 0.052
307
c SVR005 Severe Pre-Eclampsia 50 0.052
308
P TMP001 Temporal Lobe Epilepsy 50 0.052
309
P OBS001 Obstructive Jaundice 50 0.052
310
OPT003 Opiate Dependence 50 0.052
311
LRN003 Learning Disability 49 0.052
312
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.052
313
DFN270 Deafness, Dystonia, and Cerebral Hypomyelination 48 0.052
314
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.052
315
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.052
316
c CNG216 Congenital Hydrocephalus 47 0.052
317
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.052
318
SPN020 Spondylosis 46 0.052
319
P KLP003 Klippel-Feil Syndrome 46 0.052
320
c MLG068 Malignant Glioma 46 0.052
321
P HRN001 Horner's Syndrome 45 0.052
322
MXD026 Mixed Glioma 45 0.052
323
HPT004 Hepatic Coma 45 0.052
324
MCR011 Microinvasive Gastric Cancer 43 0.052
325
MDD018 Middle East Respiratory Syndrome 43 0.052
326
P MJR007 Major Affective Disorder 1 43 0.052
327
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.052
328
OCL010 Ocular Hypotension 39 0.052
329
ALG027 Al-Gazali-Bakalinova Syndrome 38 0.052
330
c MJR008 Major Affective Disorder 2 35 0.052
331
c MJR023 Major Affective Disorder 7 33 0.052
332
ENC065 Encephalitis/encephalopathy, Mild, with Reversible Myelin Vacuolization 33 0.052
333
c MJR003 Major Affective Disorder 6 33 0.052
334
c MJR006 Major Affective Disorder 5 33 0.052
335
SPN392 Spondylosis, Cervical 30 0.052
336
RSP007 Respiratory Distress Syndrome, Infant 30 0.052
337
c MJR004 Major Affective Disorder 4 28 0.052
338
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.045
339
P RHM011 Rheumatoid Arthritis 80 0.045
340
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.045
341
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.045
342
PRP027 Peripheral Vascular Disease 71 0.045
343
P SRC025 Sarcoidosis 1 70 0.045
344
OBS002 Obsessive-Compulsive Disorder 68 0.045
345
GST092 Gastroesophageal Reflux 67 0.045
346
c NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 67 0.045
347
PRP001 Propionic Acidemia 65 0.045
348
PRT036 Peritonitis 64 0.045
349
NRF007 Neurofibroma 64 0.045
350
c JVN010 Juvenile Rheumatoid Arthritis 64 0.045
351
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.045
352
KND001 Kindler Syndrome 64 0.045
353
P HYP069 Hyperparathyroidism 63 0.045
354
END041 Endometrial Adenocarcinoma 63 0.045
355
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.045
356
P TRC086 Trichohepatoenteric Syndrome 1 62 0.045
357
LVR012 Liver Cirrhosis 62 0.045
358
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.045
359
P INT143 Interstitial Cystitis 61 0.045
360
P PNC044 Pancreatitis 61 0.045
361
VRL011 Viral Infectious Disease 61 0.045
362
c JVN061 Juvenile Arthritis 60 0.045
363
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.045
364
THY029 Thyroid Carcinoma 59 0.045
365
PRT058 Pure Autonomic Failure 59 0.045
366
P CYS018 Cystitis 59 0.045
367
P INT070 Intestinal Obstruction 58 0.045
368
CHL067 Cholecystitis 57 0.045
369
THR024 Thrombosis 57 0.045
370
PHR003 Pharyngitis 57 0.045
371
P MTC069 Mitochondrial Disorders 56 0.045
372
P NRF002 Neurofibromatosis 56 0.045
373
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.045
374
END040 Endogenous Depression 55 0.045
375
CHR101 Char Syndrome 55 0.045
376
INT007 Intermediate Coronary Syndrome 55 0.045
377
CRT017 Cartilage Disease 54 0.045
378
GLC003 Glucose Intolerance 54 0.045
379
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.045
380
TRC062 Tricuspid Atresia 54 0.045
381
P LTR001 Lateral Sclerosis 54 0.045
382
PTT009 Pituitary Gland Disease 54 0.045
383
P TCD001 Tic Disorder 53 0.045
384
c CRD147 Cardiomyopathy, Familial Hypertrophic, 20 53 0.045
385
DNT012 Dental Caries 53 0.045
386
PRP080 Peripheral Artery Disease 53 0.045
387
c GLL024 Gallbladder Disease 1 53 0.045
388
P INT068 Intestinal Disease 53 0.045
389
c FML191 Familial Long Qt Syndrome 53 0.045
390
LNG031 Lung Benign Neoplasm 51 0.045
391
SCH012 Schizoaffective Disorder 50 0.045
392
RSP006 Respiratory System Disease 50 0.045
393
P SCK005 Sickle Cell Disease 50 0.045
394
PCT003 Pectus Excavatum 49 0.045
395
LPT006 Leptin Receptor Deficiency 48 0.045
396
THY128 Thyroid Tumor 47 0.045
397
CLN019 Colonic Disease 47 0.045
398
SRT004 Serotonin Syndrome 47 0.045
399
TST044 Testicular Torsion 47 0.045
400
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 46 0.045
401
SPS057 Spasticity 45 0.045
402
CRB090 Cerebral Hypoxia 44 0.045
403
c SRC023 Sarcoidosis 2 43 0.045
404
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.045
405
TRC097 Tracheomalacia 42 0.045
406
DRG024 Drug Allergy 42 0.045
407
INT276 Interatrial Communication 42 0.045
408
IDP070 Idiopathic Scoliosis 42 0.045
409
MDS018 Mediastinal Cancer 41 0.045
410
49X006 49, Xxxxy Syndrome 41 0.045
411
ADJ001 Adjustment Disorder 40 0.045
412
P INT260 Intracranial Berry Aneurysm 39 0.045
413
c TRN038 Transposition of the Great Arteries, Dextro-Looped 1 39 0.045
414
P DYS021 Dysautonomia 39 0.045
415
SPR024 Supratentorial Cancer 39 0.045
416
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 39 0.045
417
c CHR682 Chronic Bilirubin Encephalopathy 39 0.045
418
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.045
419
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.045
420
DDN027 Duodenum Disease 37 0.045
421
CRB079 Cerebrospinal Fluid Leak 35 0.045
422
DDN009 Duodenal Obstruction 34 0.045
423
SPN029 Spondylolysis 33 0.045
424
PRS064 Persistent Vegetative State 33 0.045
425
CRT009 Critical Illness Polyneuropathy 32 0.045
426
SNG003 Single Ventricular Heart 30 0.045
427
CRD220 Cardiac Valvular Defect, Developmental 29 0.045
428
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.045
429
NRF026 Neurofibromatosis, Type Iv, of Riccardi 26 0.045
430
HSB001 His Bundle Tachycardia 25 0.045
431
JVN026 Jeavons Syndrome 24 0.045
432
INT053 Intracranial Vasospasm 24 0.045
433
P INT320 Intelligence Quantitative Trait Locus 1 15 0.045
434
CRV035 Cervical Cancer 76 0.037
435
P OST002 Osteoporosis 74 0.037
436
HMN044 Human Immunodeficiency Virus Type 1 71 0.037
437
P FRG001 Fragile X Syndrome 70 0.037
438
c PNC108 Pancreatitis, Hereditary 70 0.037
439
P ANG001 Angelman Syndrome 69 0.037
440
P MYC084 Mycobacterium Tuberculosis 1 68 0.037
441
CMM004 Common Variable Immunodeficiency 68 0.037
442
P MTR014 Motor Neuron Disease 65 0.037
443
IRR002 Irritable Bowel Syndrome 65 0.037
444
TRN015 Transient Cerebral Ischemia 63 0.037
445
P LRS001 Larsen Syndrome 62 0.037
446
ATM095 Autoimmune Disease 62 0.037
447
MDD011 Mood Disorder 62 0.037
448
INT002 Intermittent Claudication 61 0.037
449
P ENC004 Encephalitis 61 0.037
450
ACQ007 Acquired Immunodeficiency Syndrome 60 0.037
451
c HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 59 0.037
452
BRN002 Bronchiolitis 59 0.037
453
ADN018 Adenoma 59 0.037
454
P HYP726 Hypercalcemia, Infantile, 1 58 0.037
455
c PRG018 Paragangliomas 1 58 0.037
456
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.037
457
P INF032 Infertility 57 0.037
458
P MYM013 Moyamoya Disease 1 57 0.037
459
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.037
460
AGN016 Aging 56 0.037
461
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.037
462
P INF037 Inflammatory Bowel Disease 54 0.037
463
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.037
464
MTN003 Motion Sickness 53 0.037
465
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.037
466
CHR073 Choreatic Disease 52 0.037
467
P PRG013 Paraganglioma 52 0.037
468
P PRR016 Pierre Robin Syndrome 52 0.037
469
PTH003 Pathologic Nystagmus 52 0.037
470
ART074 Aortic Dissection 52 0.037
471
ANK001 Ankylosis 51 0.037
472
RTN003 Retinal Ischemia 50 0.037
473
CRN030 Coronary Stenosis 50 0.037
474
PLP001 Pulpitis 49 0.037
475
CCN002 Cocaine Abuse 49 0.037
476
MTC005 Mitochondrial Metabolism Disease 49 0.037
477
c MTR002 Mitral Valve Insufficiency 48 0.037
478
RNL077 Renal Fibrosis 47 0.037
479
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.037
480
CYC008 Cyclic Vomiting Syndrome 47 0.037
481
UMB002 Umbilical Hernia 46 0.037
482
SYN036 Syncope 45 0.037
483
PLR022 Pleural Disease 45 0.037
484
MCR037 Macroglossia 45 0.037
485
ACT003 Acute Kidney Tubular Necrosis 45 0.037
486
BRN032 Brain Glioma 45 0.037
487
ASP008 Aspiration Pneumonitis 45 0.037
488
RTR001 Retrograde Amnesia 44 0.037
489
CHL012 Childhood Disintegrative Disease 44 0.037
490
EGG001 Egg Allergy 44 0.037
491
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.037
492
RST023 Resting Heart Rate, Variation in 41 0.037
493
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 41 0.037
494
ANX004 Anoxia 40 0.037
495
ALC005 Alcoholic Pancreatitis 40 0.037
496
ADN067 Adenoid Hypertrophy 39 0.037
497
FML039 Female Reproductive System Disease 39 0.037
498
HRN029 Hearing Loss, Noise-Induced 37 0.037
500
BRK012 Broken Heart Syndrome 35 0.037
501
PLM028 Pulmonary Coin Lesion 33 0.037
502
DRG001 Drug Psychosis 33 0.037
503
CLN006 Colonic Pseudo-Obstruction 32 0.037
504
c ALC016 Alcohol Sensitivity, Acute 31 0.037
505
ISL075 Isolated Pierre Robin Sequence 29 0.037
506
CMP035 Complete Atrioventricular Canal 26 0.037
507
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.037
508
NRL016 Neural Tube Defects 82 0.026
509
c DLT002 Dilated Cardiomyopathy 79 0.026
510
CNN003 Conn's Syndrome 79 0.026
511
c TBR025 Tuberous Sclerosis 1 77 0.026
512
P RTN024 Retinoblastoma 73 0.026
513
BRT054 Brittle Bone Disorder 72 0.026
514
c MCP050 Mucopolysaccharidosis, Type Ii 72 0.026
515
P JBR020 Joubert Syndrome 1 72 0.026
516
P MLT020 Multiple Sclerosis 72 0.026
517
P HYP061 Hypertrophic Cardiomyopathy 70 0.026
518
c MLT160 Multiple Endocrine Neoplasia, Type Iia 70 0.026
519
P MYP004 Myopathy 70 0.026
520
P TBR001 Tuberous Sclerosis 70 0.026
521
P KRB001 Krabbe Disease 69 0.026
522
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.026
523
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.026
524
P MYS003 Myasthenia Gravis 68 0.026
525
P MJR001 Major Depressive Disorder 68 0.026
526
P HPT021 Hepatitis 67 0.026
527
WLF001 Wolff-Parkinson-White Syndrome 66 0.026
528
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.026
529
OST159 Osteogenic Sarcoma 66 0.026
530
GLL008 Gilles De La Tourette Syndrome 66 0.026
531
P TRC072 Treacher Collins Syndrome 1 66 0.026
532
GRG001 Greig Cephalopolysyndactyly Syndrome 66 0.026
533
c MNN047 Mannosidosis, Alpha B, Lysosomal 66 0.026
534
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.026
535
ACH004 Achondroplasia 66 0.026
537
P DRM053 Dermatitis, Atopic 66 0.026
538
P PLM036 Pulmonary Fibrosis 65 0.026
539
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.026
540
KWS002 Kawasaki Disease 65 0.026
541
CLN015 Colon Adenocarcinoma 65 0.026
542
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.026
543
TBC004 Tobacco Addiction 64 0.026
544
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.026
545
P PRD008 Periodontitis 64 0.026
546
PLM031 Poliomyelitis 64 0.026
547
P CRN015 Cornelia De Lange Syndrome 64 0.026
548
P RHB003 Rhabdomyosarcoma 63 0.026
549
c DPH024 Diaphragmatic Hernia, Congenital 63 0.026
550
P HML002 Hemolytic Anemia 63 0.026
551
CNT061 Conotruncal Heart Malformations 63 0.026
552
c ACT068 Acute Cystitis 63 0.026
553
CLT003 Colitis 62 0.026
554
P DRM010 Dermatomyositis 61 0.026
555
OST003 Osteonecrosis 61 0.026
556
ART141 Arteriovenous Malformations of the Brain 61 0.026
557
HRP004 Herpes Zoster 60 0.026
558
TRG002 Trigeminal Neuralgia 60 0.026
559
SQM006 Squamous Cell Carcinoma 60 0.026
560
P PTN014 Patent Ductus Arteriosus 1 60 0.026
561
IGR001 Ige Responsiveness, Atopic 59 0.026
562
P BRS044 Breast Adenocarcinoma 59 0.026
563
P PLY006 Polydactyly 59 0.026
564
PPT005 Peptic Ulcer Disease 59 0.026
565
FBR047 Fibromyalgia 58 0.026
566
EYD002 Eye Disease 58 0.026
567
P BNC003 Bone Cancer 58 0.026
568
BRN056 Bronchopulmonary Dysplasia 57 0.026
569
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 57 0.026
570
c CRN139 Cornelia De Lange Syndrome 1 57 0.026
571
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.026
572
P OST122 Osteogenesis Imperfecta, Type Iii 57 0.026
573
CHR105 Choreoacanthocytosis 57 0.026
574
APH002 Aphasia 57 0.026
575
BLR008 Bilirubin Metabolic Disorder 57 0.026
576
CYT008 Cytomegalovirus Infection 57 0.026
577
LNN001 Lennox-Gastaut Syndrome 57 0.026
578
ADN027 Adenomyosis 56 0.026
579
BRN012 Bronchiolitis Obliterans 55 0.026
580
P SCK002 Sick Sinus Syndrome 55 0.026
581
P VNS003 Venous Insufficiency 55 0.026
582
SCH038 Schopf-Schulz-Passarge Syndrome 55 0.026
583
SYN007 Synovitis 54 0.026
584
HMS001 Hemosiderosis 54 0.026
585
LYM022 Lymphangioma 54 0.026
586
P EPD016 Epidermolysis Bullosa 53 0.026
587
CTS003 Coats Disease 53 0.026
588
P FBR031 Febrile Seizures 53 0.026
589
GST023 Gastric Ulcer 53 0.026
590
c FML008 Familial Retinoblastoma 53 0.026
591
c MCR113 Microvascular Complications of Diabetes 3 52 0.026
592
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.026
593
P TRT010 Teratoma 52 0.026
594
PRV004 Periventricular Leukomalacia 52 0.026
595
MYL001 Myelitis 51 0.026
596
ENT011 Enterocolitis 51 0.026
597
THR016 Thrombophlebitis 51 0.026
598
P PRC012 Pericardial Effusion 51 0.026
599
ACH005 Achalasia 51 0.026
600
TNG007 Tongue Carcinoma 51 0.026
601
c SCN007 Secondary Hyperparathyroidism 51 0.026
602
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.026
603
CHR005 Chorioamnionitis 51 0.026
604
BRX001 Bruxism 50 0.026
605
PST021 Postpartum Depression 50 0.026
606
STM007 Stomatitis 50 0.026
607
STT002 Status Asthmaticus 50 0.026
608
BLR001 Biliary Atresia 50 0.026
609
P MYT002 Myotonic Dystrophy 49 0.026
610
P MTC133 Mitochondrial Myopathy 49 0.026
611
P ART018 Aortic Valve Insufficiency 49 0.026
612
SNT005 Sinoatrial Node Disease 49 0.026
613
SBP001 Subependymal Giant Cell Astrocytoma 49 0.026
614
RGH001 Right Bundle Branch Block 48 0.026
615
CYS002 Cystic Lymphangioma 48 0.026
616
HMP001 Hemopericardium 48 0.026
617
HYP025 Hyperphosphatemia 48 0.026
618
c VRL012 Viral Meningitis 48 0.026
619
SXL003 Sexual Disorder 47 0.026
620
P RNL015 Renal Hypertension 47 0.026
621
c MCR120 Microvascular Complications of Diabetes 7 47 0.026
622
P CRC039 Coarctation of Aorta 47 0.026
623
MYC005 Myocardial Stunning 46 0.026
624
CRN019 Coronary Artery Vasospasm 46 0.026
625
P TRN034 Transverse Myelitis 45 0.026
626
c TRC022 Tricuspid Valve Insufficiency 45 0.026
627
CYN002 Cyanosis, Transient Neonatal 45 0.026
628
TWN001 Twin-to-Twin Transfusion Syndrome 45 0.026
629
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.026
630
THR099 Third-Degree Atrioventricular Block 45 0.026
631
EXS017 Exstrophy of Bladder 45 0.026
632
MYF001 Myofibroma 45 0.026
633
c CHR579 Chiari Malformation Type Ii 44 0.026
634
IMM064 Immunodeficiency, Common Variable, 10 44 0.026
635
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.026
636
P MTC004 Mitochondrial Encephalomyopathy 44 0.026
637
PRM003 Premature Ejaculation 44 0.026
638
RFR003 Refractive Error 43 0.026
639
PST020 Postpoliomyelitis Syndrome 43 0.026
640
P DMY001 Demyelinating Polyneuropathy 43 0.026
641
MNN017 Mononeuropathy 42 0.026
642
P CHR342 Chiari Malformation 41 0.026
643
P HYP263 Hypersomnia 41 0.026
644
c MCR130 Microvascular Complications of Diabetes 6 41 0.026
645
c MCR133 Microvascular Complications of Diabetes 4 41 0.026
646
PRS063 Paresthesia 41 0.026
647
P RRH023 Rare Hereditary Hemochromatosis 41 0.026
648
P SCL057 Scoliosis, Isolated 1 41 0.026
649
CRN322 Coronavirus Infectious Disease 40 0.026
650
OST115 Osteonecrosis of the Jaw 40 0.026
651
SPN221 Spina Bifida Occulta 39 0.026
652
MLG086 Malignant Hyperthermia Susceptibility 39 0.026
653
WLL004 Wallerian Degeneration 39 0.026
654
ALL014 Allergic Encephalomyelitis 38 0.026
655
c ACT159 Acute Transverse Myelitis 38 0.026
656
OVR094 Ovarian Epithelial Cancer 38 0.026
657
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.026
658
P CRB088 Cerebral Atrophy 37 0.026
659
c MND002 Mandibuloacral Dysplasia with Type B Lipodystrophy 36 0.026
660
PLC002 Plica Syndrome 36 0.026
661
RBN014 Robin Sequence with Cleft Mandible and Limb Anomalies 35 0.026
662
SCN049 Second-Degree Atrioventricular Block 35 0.026
663
AMR003 Amaurosis Fugax 34 0.026
664
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.026
666
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.026
667
OVR109 Ovarian Germ Cell Teratoma 32 0.026
668
P RRL003 Rare Lymphatic Malformation 31 0.026
669
TRT017 Teratoma, Ovarian 29 0.026
670
PST092 Posttransplant Acute Limbic Encephalitis 29 0.026
671
P ATR081 Atrial Standstill 28 0.026
672
CCN009 Cocaine Intoxication 27 0.026
673
MDR006 Moderate and Severe Traumatic Brain Injury 27 0.026
674
STR033 Storm Syndrome 26 0.026
675
ACT162 Acute Sensory Ataxic Neuropathy 26 0.026
676
FCL074 Facial Spasm 23 0.026
677
DBL004 Double Discordia 23 0.026
678
P ZNC008 Zinc Finger Protein 1 22 0.026
679
EPB002 Epiblepharon 17 0.026
680
VNT036 Ventilator-Induced Diaphragmatic Dysfunction 17 0.026
681
IDP022 Idiopathic Spinal Cord Herniation 17 0.026
Content
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