Search results for Meperidine

398 hits were found for Meperidine

# Family MCID Name MIFTS Score
1
PNG002 Pain Agnosia 51 25.360
2
c MGR028 Migraine with or Without Aura 1 64 6.049
3
P SCK005 Sickle Cell Disease 56 5.804
4
SBC016 Subacute Delirium 43 5.712
5
P HDC001 Headache 57 5.656
6
AMN003 Amnestic Disorder 54 5.273
7
48X005 48,xyyy 39 5.181
8
P PNC044 Pancreatitis 61 5.054
9
P SZR006 Seizure Disorder 70 4.939
10
c ACT027 Acute Pancreatitis 60 4.787
11
P CHR345 Chronic Pain 50 4.674
12
P TRM003 Tremor 48 4.573
13
SRT004 Serotonin Syndrome 54 4.429
14
SCK003 Sickle Cell Anemia 74 3.936
15
P MYC033 Myoclonus 47 3.866
16
CRV035 Cervical Cancer 73 3.329
17
BCK006 Back Pain 47 3.252
18
47X002 47,xyy 48 2.908
19
ING001 Inguinal Hernia 59 2.881
20
BLR004 Biliary Dyskinesia 37 2.876
21
P PRK039 Parkinsonism 55 2.853
22
CHL039 Choledocholithiasis 37 2.806
23
PLM129 Pulmonary Disease, Chronic Obstructive 74 2.779
24
OCL069 Ocular Motor Apraxia 57 2.772
25
INF118 Inflammatory Myopathy with Abundant Macrophages 27 2.567
26
DRG003 Drug Dependence 46 2.567
27
P CRD119 Cardiac Arrest 67 2.550
28
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 2.536
29
AGN016 Aging 54 2.536
30
c PNS012 Paine Syndrome 60 2.503
31
c EPS039 Episodic Pain Syndrome, Familial, 1 42 2.503
32
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 2.409
33
PRS021 Prostatic Adenoma 43 2.373
34
P MYP004 Myopathy 67 2.323
35
GST092 Gastroesophageal Reflux 61 2.300
36
CHL067 Cholecystitis 60 2.300
37
P VSC011 Vasculitis 61 2.223
38
ART140 Arteries, Anomalies of 53 2.185
39
LPP008 Lipoprotein Quantitative Trait Locus 65 2.185
40
P VSC007 Vascular Disease 63 2.185
41
P EXN002 Exanthem 58 2.142
42
VRC005 Varicose Veins 60 2.142
43
P LCT001 Lactic Acidosis 51 2.142
44
PLP001 Pulpitis 48 2.028
45
HPT004 Hepatic Coma 43 1.965
46
c MLT068 Multiple Mitochondrial Dysfunctions Syndrome 1 45 1.942
47
RHB024 Rhabdomyosarcoma 2 67 1.942
48
CHL065 Cholangiocarcinoma 58 1.942
49
P GLL020 Gallbladder Disease 56 1.942
50
P MLT027 Multiple Mitochondrial Dysfunctions Syndrome 36 1.942
51
INT079 Intrahepatic Cholangiocarcinoma 51 1.942
52
P CRV039 Cervicitis 52 1.918
53
RTR001 Retrograde Amnesia 41 1.867
54
NPH009 Nephrolithiasis 54 1.867
55
ASP007 Aspiration Pneumonia 49 1.867
56
HPT019 Hepatic Encephalopathy 59 1.867
57
P PYL005 Pyelonephritis 57 1.867
58
URT014 Ureterolithiasis 43 1.867
59
HDN002 Head Injury 44 1.867
60
FTD001 Foot Drop 35 1.867
61
PRT058 Pure Autonomic Failure 58 1.867
62
P CTR002 Cataract 60 1.822
63
ILS001 Ileus 50 1.799
65
ALC006 Alcoholic Hepatitis 61 1.760
66
LYM017 Lyme Disease 62 1.760
67
P SBS003 Substance Abuse 54 1.760
68
CYN002 Cyanosis, Transient Neonatal 43 1.728
69
P CRN300 Coronary Heart Disease 1 73 1.686
70
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.686
71
c CRN243 Carney Complex, Type 1 53 1.686
72
c HYP724 Hyperlipoproteinemia, Type Iii 67 1.686
73
DNT012 Dental Caries 53 1.686
74
ANR040 Aneurysm 61 1.686
75
CHL079 Children's Interstitial Lung Disease 26 1.686
76
P PRK057 Parkinson Disease, Late-Onset 80 1.643
77
LNG099 Lung Disease 62 1.643
78
DYS073 Dysphagia 53 1.643
79
P STR020 Strabismus 56 1.578
80
MCH006 Mechanical Strabismus 40 1.578
81
DFC004 Deficiency Anemia 74 1.568
82
END040 Endogenous Depression 55 1.568
83
MNT002 Mental Depression 57 1.568
84
NDL024 Nodal Marginal Zone Lymphoma 37 1.509
85
c ACT073 Acute Leukemia 58 1.509
86
c ACT075 Acute Myocardial Infarction 56 1.509
87
P URT039 Urticaria 58 1.509
88
PTH003 Pathologic Nystagmus 52 1.509
89
OPD006 Opioid Addiction 48 1.509
90
URL001 Urolithiasis 46 1.505
91
RNL114 Renal Cell Carcinoma, Nonpapillary 80 1.505
92
CNS004 Constipation 56 1.497
93
LPT014 Leptin Deficiency or Dysfunction 78 1.411
94
PRT037 Pertussis 65 1.411
95
P ALC033 Alcohol Use Disorder 61 1.411
96
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 1.350
97
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 1.350
98
P NRP001 Neuropathy 60 1.350
99
P LNG028 Long Qt Syndrome 64 1.350
100
HYP264 Hypertonia 36 1.350
101
P MLG056 Malignant Hyperthermia 66 1.320
102
PNM008 Pneumothorax 54 1.320
103
CHR005 Chorioamnionitis 50 1.222
104
OPD001 Opioid Abuse 44 1.222
105
c GLL024 Gallbladder Disease 1 52 1.213
106
INT146 Intervertebral Disc Disease 63 1.213
107
P KDN018 Kidney Disease 72 1.213
108
LVR012 Liver Cirrhosis 63 1.213
109
c ATR087 Atrial Standstill 1 74 1.144
110
KRK001 Krukenberg Carcinoma 39 1.144
111
P GST053 Gastric Cancer 83 1.125
112
ADN018 Adenoma 59 1.125
113
MCR011 Microinvasive Gastric Cancer 41 1.125
114
PPL001 Papillary Adenoma 44 1.125
115
VRS002 Virus-Associated Trichodysplasia Spinulosa 30 1.116
116
PRT036 Peritonitis 65 1.116
117
APP008 Appendicitis 62 1.116
118
CYT002 Cytokine Deficiency 43 1.116
119
PST021 Postpartum Depression 50 1.069
120
c FNC043 Fanconi Anemia, Complementation Group E 62 1.069
121
SPR126 Superior Semicircular Canal Dehiscence 41 1.069
122
P GRF003 Graft-Versus-Host Disease 71 1.069
123
NRT001 Neurotic Disorder 56 1.069
124
ATX019 Ataxia with Vitamin E Deficiency 44 1.069
125
HML018 Homologous Wasting Disease 21 1.069
126
DPR016 Depression 65 1.069
127
AND005 Androgen Insensitivity Syndrome, Mild 21 1.069
128
c HMG029 Hemoglobin Se Disease 40 1.069
129
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 1.069
130
P SCL018 Scoliosis 57 1.006
131
ACQ007 Acquired Immunodeficiency Syndrome 59 1.006
132
DDN006 Duodenitis 50 1.006
133
CLF027 Cleft Palate, Isolated 64 0.998
134
P CLR023 Colorectal Cancer 100 0.998
135
P SLP006 Sleep Apnea 69 0.998
136
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 46 0.998
137
PNM010 Pneumothorax, Primary Spontaneous 58 0.998
138
P MVM001 Movement Disease 61 0.998
139
END086 End Stage Renal Disease 52 0.998
140
CHL004 Cholelithiasis 49 0.998
141
P MLN008 Melanoma 76 0.998
142
CLN015 Colon Adenocarcinoma 65 0.998
143
P RSP003 Respiratory Failure 74 0.998
144
ALC005 Alcoholic Pancreatitis 38 0.998
145
P PRP029 Porphyria 60 0.998
146
ANX004 Anoxia 40 0.912
147
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.864
148
RFR010 Refractory Anemia 49 0.864
149
P THL005 Thalassemia 56 0.864
150
PRS129 Prostatic Hyperplasia, Benign 49 0.864
151
ADN027 Adenomyosis 57 0.864
152
KPS004 Kaposi Sarcoma 77 0.864
153
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 0.864
154
CPR004 Coproporphyria, Hereditary 57 0.864
155
P MYC007 Myocardial Infarction 70 0.864
156
c CHR684 Chronic Kidney Disease 69 0.864
157
P GST044 Gastritis 55 0.864
158
P INT070 Intestinal Obstruction 57 0.864
159
CRB004 Cerebral Artery Occlusion 45 0.864
160
P NTR004 Neutropenia 63 0.864
161
NRL004 Neuroleptic Malignant Syndrome 52 0.864
162
P END044 Endometriosis 62 0.864
163
PRS045 Prostatic Hypertrophy 53 0.864
164
CLN019 Colonic Disease 47 0.864
165
PLM010 Pulmonary Edema 55 0.864
166
ACT017 Acute Chest Syndrome 50 0.864
167
CHR073 Choreatic Disease 54 0.864
168
HYP080 Hypogonadism 50 0.864
169
SPN186 Spinal Cord Injury 61 0.706
170
P AVS003 Avascular Necrosis 41 0.706
171
P MYM013 Moyamoya Disease 1 59 0.706
172
P MYS003 Myasthenia Gravis 68 0.706
173
c SPN225 Spondyloarthropathy 1 70 0.706
174
APN008 Apnea, Obstructive Sleep 67 0.706
175
LMY002 Leiomyoma 51 0.706
176
P DYS154 Dystonia 64 0.706
177
ASP008 Aspiration Pneumonitis 42 0.706
178
PRP007 Priapism 47 0.706
179
P MTC133 Mitochondrial Myopathy 50 0.706
180
PRL008 Paralytic Ileus 45 0.706
181
SPN051 Spondylitis 51 0.706
182
OST012 Osteoarthritis 77 0.706
183
P MGR003 Migraine with Aura 52 0.706
184
INF009 Inflammatory Spondylopathy 30 0.706
185
P HMN010 Hemangioma 62 0.706
186
P DDN001 Duodenal Ulcer 53 0.706
187
P MTH007 Methemoglobinemia 46 0.706
188
CDQ001 Cauda Equina Syndrome 37 0.706
189
PLM028 Pulmonary Coin Lesion 30 0.706
190
c ESS001 Essential Tremor 57 0.706
191
P OVR046 Ovarian Cyst 46 0.706
192
P PNM007 Pneumonia 67 0.706
193
ACT058 Active Peptic Ulcer Disease 56 0.706
194
MRP001 Morphine Dependence 42 0.706
195
MMM001 Mammary Paget's Disease 53 0.706
196
STT001 Status Epilepticus 59 0.706
197
c SVR005 Severe Pre-Eclampsia 50 0.706
198
P ACT105 Acute Mountain Sickness 52 0.706
199
P BLR006 Biliary Tract Disease 46 0.706
200
IRR002 Irritable Bowel Syndrome 65 0.706
201
SPL018 Splenomegaly 49 0.706
202
P MTC069 Mitochondrial Disorders 57 0.706
203
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.645
204
MTB004 Metabolic Acidosis 48 0.645
205
PHN003 Phenylketonuria 76 0.645
206
P PLM034 Pulmonary Emphysema 58 0.645
207
c VRL010 Viral Hepatitis 53 0.645
208
THR016 Thrombophlebitis 50 0.645
209
PRP016 Paraplegia 52 0.645
210
ALL029 Allergic Disease 59 0.645
211
TRN015 Transient Cerebral Ischemia 63 0.645
212
BRK012 Broken Heart Syndrome 42 0.645
213
CRC006 Carcinoid Syndrome 55 0.645
214
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.508
215
SQM013 Squamous Cell Carcinoma, Head and Neck 73 0.508
216
STR067 Stroke, Ischemic 80 0.508
217
HMN044 Human Immunodeficiency Virus Type 1 78 0.508
218
MSC007 Muscle Hypertrophy 64 0.508
219
c XNT010 Xanthinuria, Type I 52 0.508
220
RNL065 Renal Cell Carcinoma, Papillary, 1 79 0.508
221
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 70 0.508
222
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.508
223
P ANR048 Aniridia 1 64 0.508
224
c PLM150 Pulmonary Alveolar Proteinosis, Acquired 40 0.508
225
c HPT003 Hepatitis a 63 0.508
226
ANT039 Antisynthetase Syndrome 55 0.508
227
P TRN020 Turner Syndrome 67 0.508
228
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.508
229
HNT002 Hantavirus Pulmonary Syndrome 55 0.508
230
P HPT021 Hepatitis 69 0.508
231
CRB039 Cerebrovascular Disease 66 0.508
232
P INF032 Infertility 57 0.508
233
ISC004 Ischemia 61 0.508
234
P KDN017 Kidney Cancer 61 0.508
235
IDP070 Idiopathic Scoliosis 42 0.508
236
VGN023 Vaginitis 56 0.508
237
ASC009 Ascites, Chylous 32 0.499
238
PCH007 Pouchitis 42 0.499
239
SPN340 Spontaneous Intracranial Hypotension 27 0.499
240
MTC005 Mitochondrial Metabolism Disease 45 0.499
241
P DCR003 Dacryoadenitis 44 0.499
242
HPT070 Hepatosplenic T-Cell Lymphoma 36 0.499
243
SPS057 Spasticity 42 0.499
244
P NSP012 Nasopharyngeal Carcinoma 61 0.499
245
SJG002 Sjogren-Larsson Syndrome 54 0.499
246
CRD223 Cardiac Arrhythmia 63 0.499
247
CRD132 Cardiac Conduction Defect 60 0.499
248
P LPR021 Leprosy 3 71 0.499
249
RTN072 Retinohepatoendocrinologic Syndrome 22 0.499
250
ISP002 Isoproterenol-Mediated Vasodilatation 8 0.499
251
RTN017 Retinal Detachment 60 0.499
252
P PHC003 Pheochromocytoma 69 0.499
253
c PRG042 Progressive Familial Heart Block, Type Ia 66 0.499
254
ALC007 Alcohol Dependence 66 0.499
255
P TMP003 Temporal Arteritis 69 0.499
256
MRL006 Meralgia Paraesthetica, Familial 27 0.499
257
NRD100 Neurodevelopmental, Jaw, Eye, and Digital Syndrome 49 0.499
258
PRP027 Peripheral Vascular Disease 71 0.499
259
c BTT014 Beta-Thalassemia 72 0.499
260
P URN019 Urinary Tract Infection 49 0.499
261
P PLY014 Polycystic Kidney Disease 69 0.499
262
c BRN143 Bronchiectasis 1 23 0.499
263
WTH001 Withdrawal Disorder 48 0.499
264
ECT026 Ectopic Pregnancy 48 0.499
265
BNR002 Bone Resorption Disease 47 0.499
266
SXL003 Sexual Disorder 49 0.499
267
HYP025 Hyperphosphatemia 48 0.499
268
SNT005 Sinoatrial Node Disease 47 0.499
269
TRD006 Tardive Dyskinesia 53 0.499
270
SPN354 Spinal Arachnoiditis 36 0.499
271
P PLV020 Pelvic Organ Prolapse 58 0.499
272
P LRY029 Laryngomalacia 48 0.499
273
P MJR001 Major Depressive Disorder 68 0.499
274
ENT011 Enterocolitis 55 0.499
275
c PNC106 Pancreatic Agenesis 1 51 0.499
276
THR100 Thrombocytopenic Purpura, Autoimmune 61 0.499
277
WLF001 Wolff-Parkinson-White Syndrome 65 0.499
278
P SRC025 Sarcoidosis 1 71 0.499
279
c NMN015 Niemann-Pick Disease, Type C1 68 0.499
280
P CNG499 Congenital Anomalies of Kidney and Urinary Tract 2 52 0.499
281
INT051 Intussusception 52 0.499
282
ACH004 Achondroplasia 66 0.499
283
P PTN014 Patent Ductus Arteriosus 1 59 0.499
284
ADR040 Adrenal Gland Pheochromocytoma 46 0.499
285
ADR041 Adrenal Cortical Adenoma 49 0.499
286
BCT022 Bacterial Infectious Disease 56 0.499
287
URC012 Urachal Sinus 13 0.499
288
CRD137 Cardiogenic Shock 56 0.499
289
CRY014 Cryptococcal Meningitis 48 0.499
290
CRH001 Crohn's Disease 80 0.499
291
URM002 Uremia 47 0.499
292
INT003 Intracranial Hypotension 36 0.499
293
SCL017 Sclerosing Hemangioma 29 0.499
294
SPC005 Speech Disorder 45 0.499
295
INT075 Intracranial Hypertension 53 0.499
296
ULC004 Ulcerative Colitis 74 0.499
297
P CHL066 Cholangitis 52 0.499
298
P HML002 Hemolytic Anemia 62 0.499
299
PST092 Posttransplant Acute Limbic Encephalitis 28 0.499
300
GLL048 Glial Tumor 52 0.499
301
P HMR005 Hemorrhoid 49 0.499
302
P ALP008 Alopecia 54 0.499
303
P RRH023 Rare Hereditary Hemochromatosis 54 0.499
304
P VNT002 Ventricular Septal Defect 58 0.499
305
HRT011 Heart Septal Defect 49 0.499
306
P LVR013 Liver Disease 69 0.499
307
HYP066 Hyperglycemia 61 0.499
308
PLM001 Pulmonary Tuberculosis 69 0.499
309
GNG008 Ganglioneuroblastoma 47 0.499
310
VGN019 Vaginal Discharge 47 0.499
311
PLR007 Pleural Empyema 51 0.499
312
CLN006 Colonic Pseudo-Obstruction 30 0.499
313
P ACN011 Acne 57 0.499
314
MYF001 Myofibroma 42 0.499
315
HYP005 Hypokalemia 55 0.499
316
RDC002 Radiculopathy 52 0.499
317
ADN009 Adenosquamous Carcinoma 48 0.499
318
MYL001 Myelitis 50 0.499
319
TRC005 Tracheal Stenosis 43 0.499
320
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 0.499
321
GST027 Gastric Lymphoma 46 0.499
322
PLR008 Pleurisy 50 0.499
323
LFT001 Left Bundle Branch Hemiblock 47 0.499
324
c PRC016 Pre-Eclampsia 65 0.499
325
P MGR001 Migraine Without Aura 49 0.499
326
TLN003 Telangiectasis 51 0.499
327
P DMN002 Dementia 66 0.499
328
GT001 Gout 64 0.499
329
HMS001 Hemosiderosis 48 0.499
330
CRY005 Cryptococcosis 60 0.499
331
ARC002 Arachnoiditis 50 0.499
332
P ESP024 Esophagitis 60 0.499
333
GTR002 Goiter 53 0.499
334
CNN003 Conn's Syndrome 79 0.499
335
ATY001 Atypical Depressive Disorder 45 0.499
336
CMP006 Complex Partial Epilepsy 36 0.499
337
BLR008 Bilirubin Metabolic Disorder 57 0.499
338
MLN003 Melancholia 41 0.499
339
P ATR010 Atrial Heart Septal Defect 58 0.499
340
P NMN002 Niemann-Pick Disease 60 0.499
341
PYL006 Pyloric Stenosis 48 0.499
342
NRT004 Neuritis 53 0.499
343
P GCH001 Gaucher's Disease 70 0.499
344
FCL014 Focal Epilepsy 53 0.499
345
NNT012 Neonatal Jaundice 53 0.499
346
ACT078 Acute Porphyria 49 0.499
347
OPT003 Opiate Dependence 49 0.499
348
SPL009 Splenic Sequestration 34 0.499
349
P HYD006 Hydrocephalus 61 0.499
350
P BND020 Bone Disease 59 0.499
351
P MYG005 Myoglobinuria 40 0.499
352
MCS002 Mucositis 56 0.499
353
LPR001 Lepromatous Leprosy 49 0.499
354
DSC004 Discitis 34 0.499
355
QFV001 Q Fever 62 0.499
356
CYS010 Cystinosis 62 0.499
357
CNG034 Congestive Heart Failure 69 0.499
358
P CNJ013 Conjunctivitis 66 0.499
359
P RHN004 Rhinitis 57 0.499
360
HYD001 Hydranencephaly 43 0.499
361
PRP030 Purpura 54 0.499
362
P CYS039 Cystic Kidney Disease 53 0.499
363
c ACT071 Acute Kidney Failure 60 0.499
364
P GLL018 Gallbladder Cancer 53 0.499
365
PNC034 Pancreas Disease 50 0.499
366
c HMG001 Hemoglobin C Disease 41 0.499
367
LYS002 Lysosomal Storage Disease 51 0.499
368
P OBS001 Obstructive Jaundice 48 0.499
369
P SCK002 Sick Sinus Syndrome 55 0.499
370
TBR009 Tuberculous Empyema 23 0.499
371
P PTS002 Ptosis 52 0.499
372
P ART005 Arteriovenous Malformation 65 0.499
373
MGC001 Megacolon 48 0.499
374
P NRM002 Normal Pressure Hydrocephalus 49 0.499
375
GST023 Gastric Ulcer 52 0.499
376
QDR001 Quadriplegia 50 0.499
377
P BNC003 Bone Cancer 58 0.499
378
CRB037 Cerebral Palsy 67 0.499
379
P RCT021 Rectum Cancer 54 0.499
380
HYP060 Hyperinsulinism 54 0.499
381
END028 Endemic Goiter 41 0.499
382
P MNN013 Meningitis 65 0.499
383
P BRN022 Bronchiectasis 60 0.499
384
P CMP008 Compartment Syndrome 50 0.499
385
GRN017 Granulocytopenia 42 0.499
386
HYD005 Hydrocele 46 0.499
387
INT059 Internal Hemorrhoid 35 0.499
388
P DCR004 Dacryocystitis 36 0.499
389
HNS001 Hansen's Disease 32 0.499
390
HRS011 Horseshoe Kidney 31 0.499
391
OPS006 Opsoclonus-Myoclonus Syndrome 48 0.499
392
CRB090 Cerebral Hypoxia 42 0.499
393
FLP002 Floppy Infant Syndrome 13 0.499
394
P DYS021 Dysautonomia 38 0.499
395
BRN056 Bronchopulmonary Dysplasia 56 0.499
396
INF043 Infantile Apnea 21 0.499
397
GLM045 Glioma 63 0.499
398
PRN019 Perinatal Necrotizing Enterocolitis 60 0.499
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