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Search results for Desflurane

381 hits were found for Desflurane

# Family MCID Name MIFTS Score
1
SBC016 Subacute Delirium 43 11.791
2
PNG002 Pain Agnosia 51 9.527
3
P MLG056 Malignant Hyperthermia 66 7.092
4
P STR020 Strabismus 56 6.653
5
MCH006 Mechanical Strabismus 40 6.653
6
P SCL018 Scoliosis 57 6.330
7
AMN003 Amnestic Disorder 54 6.316
8
ISC004 Ischemia 61 6.119
9
LPT014 Leptin Deficiency or Dysfunction 78 4.902
10
P CLR023 Colorectal Cancer 100 4.181
11
48X005 48,xyyy 39 4.106
12
P ALZ034 Alzheimer Disease 87 4.063
13
ART140 Arteries, Anomalies of 53 3.809
14
LPP008 Lipoprotein Quantitative Trait Locus 65 3.809
15
HMF011 Hemifacial Spasm, Familial 33 3.781
16
P HMF004 Hemifacial Spasm 38 3.781
17
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 3.663
18
ING001 Inguinal Hernia 59 3.663
19
P HRT032 Heart Disease 81 3.656
20
P CRD119 Cardiac Arrest 67 3.636
21
HYP066 Hyperglycemia 61 3.609
22
ANR040 Aneurysm 61 3.582
23
P HPT023 Hepatocellular Carcinoma 96 3.441
24
P ADL010 Adult Respiratory Distress Syndrome 71 3.441
25
LVR012 Liver Cirrhosis 63 3.440
26
47X002 47,xyy 48 3.437
27
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 3.404
28
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 3.404
29
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 3.404
30
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 3.404
31
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 3.404
32
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 3.404
33
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 3.404
34
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 3.404
35
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 3.404
36
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 3.404
37
INT075 Intracranial Hypertension 53 3.395
38
CYT002 Cytokine Deficiency 43 3.377
39
ANX004 Anoxia 40 3.279
40
P LVR013 Liver Disease 69 3.255
41
P PNC035 Pancreatic Cancer 86 3.207
42
CHL065 Cholangiocarcinoma 58 3.207
43
INT079 Intrahepatic Cholangiocarcinoma 51 3.207
44
P BRS047 Breast Cancer 98 3.188
45
HYP266 Hypoxia 57 3.157
46
P LRY019 Laryngitis 53 3.146
47
PTT037 Pituitary Tumors 44 3.145
48
IDP070 Idiopathic Scoliosis 42 3.129
49
AGN016 Aging 54 3.124
50
TRM010 Traumatic Brain Injury 51 3.093
51
BRN071 Brain Injury 50 3.093
52
MTB004 Metabolic Acidosis 48 3.032
53
P CTR002 Cataract 60 3.027
54
CRB004 Cerebral Artery Occlusion 45 2.970
55
P KDN018 Kidney Disease 72 2.828
56
P PHC003 Pheochromocytoma 69 2.772
57
ADR040 Adrenal Gland Pheochromocytoma 46 2.772
58
IDP022 Idiopathic Spinal Cord Herniation 17 2.772
59
P NRP001 Neuropathy 60 2.748
60
P OVR046 Ovarian Cyst 46 2.748
61
P ENT005 Entropion 34 2.719
62
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 2.671
63
P SLP006 Sleep Apnea 69 2.637
64
P MYS003 Myasthenia Gravis 68 2.552
65
P SPP010 Suppressor of Tumorigenicity 3 51 2.552
66
P MYC007 Myocardial Infarction 70 2.472
67
c HPT003 Hepatitis a 63 2.471
68
P HPT021 Hepatitis 69 2.471
69
P ANR048 Aniridia 1 64 2.459
70
CRN030 Coronary Stenosis 50 2.457
71
END086 End Stage Renal Disease 52 2.433
72
P GST053 Gastric Cancer 83 2.388
73
STT001 Status Epilepticus 59 2.388
74
P RSP003 Respiratory Failure 74 2.384
75
CRB086 Cerebral Aneurysms 40 2.384
76
P FNG006 Feingold Syndrome 1 62 2.351
77
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 2.351
78
MTN003 Motion Sickness 51 2.308
79
MYL020 Myelomeningocele 51 2.308
80
P GLL020 Gallbladder Disease 56 2.308
81
ADL002 Adult Syndrome 70 2.254
82
c ACT071 Acute Kidney Failure 60 2.233
83
OCL069 Ocular Motor Apraxia 57 2.228
84
P BCL017 B-Cell Lymphoma 59 2.228
85
RHB024 Rhabdomyosarcoma 2 67 2.215
86
CRB009 Cerebritis 43 2.215
87
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 2.204
88
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 2.144
89
WLF001 Wolff-Parkinson-White Syndrome 65 2.144
90
c HYP595 Hypertension, Essential 85 2.130
91
P CRN300 Coronary Heart Disease 1 73 2.100
92
P VSC007 Vascular Disease 63 2.095
93
CRD223 Cardiac Arrhythmia 63 2.055
94
ATR089 Atrioventricular Dissociation 21 2.055
95
HLT002 Halothane Hepatitis 31 2.055
96
MDD018 Middle East Respiratory Syndrome 44 2.055
97
HYP056 Hypoglycemia 65 2.055
98
CD4008 Cd4/cd8 T-Cell Ratio 19 1.960
99
P PRS049 Persistent Mullerian Duct Syndrome 52 1.960
100
MLG086 Malignant Hyperthermia Susceptibility 39 1.960
101
MYC005 Myocardial Stunning 46 1.960
102
ANG049 Angioedema Induced by Ace Inhibitors 40 1.934
103
ANX010 Anxiety 70 1.915
104
P PTT006 Pituitary Adenoma 55 1.915
105
ART016 Aortic Aneurysm 68 1.915
106
ADN018 Adenoma 59 1.915
107
PHR003 Pharyngitis 58 1.915
108
c PNS012 Paine Syndrome 60 1.877
109
c EPS039 Episodic Pain Syndrome, Familial, 1 42 1.877
110
c ATR087 Atrial Standstill 1 74 1.858
111
GLL048 Glial Tumor 52 1.858
112
P LCT001 Lactic Acidosis 51 1.858
113
ILS001 Ileus 50 1.858
114
P HYP040 Hypospadias 51 1.858
115
P OBS001 Obstructive Jaundice 48 1.858
116
GLM045 Glioma 63 1.858
117
CRB039 Cerebrovascular Disease 66 1.807
118
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.792
119
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 1.792
120
c CHR684 Chronic Kidney Disease 69 1.792
121
P BLD124 Bleeding Disorder, Platelet-Type, 11 67 1.768
122
c EXD008 Exudative Vitreoretinopathy 1 71 1.748
123
ESP021 Esophageal Cancer 83 1.748
124
ACT032 Acute Hemorrhagic Leukoencephalitis 33 1.748
125
c ACT075 Acute Myocardial Infarction 56 1.748
126
TXC002 Toxic Encephalopathy 52 1.748
127
GLB002 Glioblastoma 67 1.748
128
PRL008 Paralytic Ileus 45 1.748
129
ATN004 Autonomic Neuropathy 42 1.748
130
PRT013 Portal Hypertension 59 1.748
131
TTH004 Tethered Spinal Cord Syndrome 41 1.748
132
INT030 Intracranial Aneurysm 55 1.748
133
PRT018 Portal Vein Thrombosis 50 1.748
134
CHL068 Cholestasis 61 1.748
135
PRS064 Persistent Vegetative State 33 1.748
136
STR067 Stroke, Ischemic 80 1.734
137
ANT039 Antisynthetase Syndrome 55 1.724
138
CRV002 Cervix Uteri Carcinoma in Situ 47 1.639
139
CRV045 Cervical Intraepithelial Neoplasia 39 1.639
140
PRP083 Porphyria, Acute Intermittent 65 1.625
141
P MSC005 Muscular Dystrophy 67 1.625
142
RTN003 Retinal Ischemia 49 1.625
143
EXT054 Extra-Adrenal Pheochromocytoma 32 1.625
144
P INF032 Infertility 57 1.625
145
P PRP029 Porphyria 60 1.625
146
CRB037 Cerebral Palsy 67 1.625
147
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 1.622
148
APN008 Apnea, Obstructive Sleep 67 1.622
149
P LNG032 Lung Cancer 98 1.582
150
c HYP724 Hyperlipoproteinemia, Type Iii 67 1.582
151
P THY032 Thyroiditis 57 1.582
152
P ART022 Arthritis 71 1.582
153
c ACT027 Acute Pancreatitis 60 1.582
154
P PNC044 Pancreatitis 61 1.582
155
AND005 Androgen Insensitivity Syndrome, Mild 21 1.582
156
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 1.582
157
P MLT020 Multiple Sclerosis 79 1.566
158
ATM095 Autoimmune Disease 61 1.487
159
P PLM037 Pulmonary Hypertension 72 1.487
160
NNL006 Non-Alcoholic Steatohepatitis 54 1.487
161
HPT004 Hepatic Coma 43 1.487
162
ACS001 Acoustic Neuroma 56 1.487
163
PRP016 Paraplegia 52 1.487
164
CVR006 Cavernous Hemangioma 51 1.487
165
P HMN010 Hemangioma 62 1.487
166
HPT019 Hepatic Encephalopathy 59 1.487
167
P TCD001 Tic Disorder 49 1.487
168
NRM004 Neuroma 49 1.487
169
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 1.466
170
P OPT006 Optic Nerve Disease 58 1.400
171
P URF003 Urofacial Syndrome 1 56 1.397
172
P BLD134 Bladder Cancer 79 1.397
173
NRD100 Neurodevelopmental, Jaw, Eye, and Digital Syndrome 49 1.397
174
P INT260 Intracranial Berry Aneurysm 40 1.397
175
BRD001 Brody Myopathy 55 1.397
176
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 36 1.397
177
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 1.397
178
PRP001 Propionic Acidemia 65 1.397
179
c ART101 Aortic Valve Disease 2 66 1.397
180
BHR001 Behr Syndrome 51 1.397
181
BLR028 Biliary Atresia, Extrahepatic 36 1.397
182
PCT003 Pectus Excavatum 46 1.397
183
LWR018 Lower Urinary Tract Obstruction, Congenital 39 1.397
184
P BLD062 Bile Duct Cancer 67 1.397
185
SPR024 Supratentorial Cancer 39 1.397
186
HRT012 Heart Valve Disease 53 1.397
187
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 1.397
188
VGN020 Vaginal Disease 48 1.397
189
BLR001 Biliary Atresia 55 1.397
190
PPL001 Papillary Adenoma 44 1.397
191
URN010 Urinary Tract Obstruction 55 1.397
192
PTT009 Pituitary Gland Disease 53 1.397
193
URN009 Urinary System Disease 47 1.397
194
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 43 1.322
195
P TRM003 Tremor 48 1.322
196
NRM005 Neuromuscular Disease 63 1.322
197
TXC005 Toxic Shock Syndrome 62 1.322
198
c HRD010 Hereditary Spastic Paraplegia 66 1.322
199
DMY004 Demyelinating Disease 50 1.322
200
P MYT002 Myotonic Dystrophy 51 1.322
201
P CMP008 Compartment Syndrome 50 1.322
202
MYT011 Myotonia 39 1.322
203
P OVR042 Ovarian Cancer 88 1.269
204
OCL006 Ocular Hypertension 53 1.269
205
CRT013 Carotid Stenosis 51 1.216
206
NRN002 Neuronitis 31 1.164
207
WTH001 Withdrawal Disorder 48 1.159
208
NRL016 Neural Tube Defects 81 1.159
209
P SLP005 Sleep Disorder 61 1.159
210
c ACT134 Acute Liver Failure 59 1.107
211
OTT002 Otitis Media 71 1.107
213
INS023 Insensitivity to Pain, Congenital, with Anhidrosis 57 1.107
214
PNS018 Pain Sensitivity Quantitative Trait Locus 1 23 1.107
215
ANH002 Anhidrosis 46 1.107
216
RHM001 Rheumatic Fever 59 1.107
217
CHL122 Cholesteatoma of Middle Ear 51 1.107
218
P HDC001 Headache 57 1.107
219
P TRN020 Turner Syndrome 67 1.074
220
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 46 1.036
221
c ALZ056 Alzheimer Disease 3 55 1.036
222
P NRB001 Neuroblastoma 66 1.036
223
P DYS154 Dystonia 64 1.036
224
P VNT002 Ventricular Septal Defect 58 1.036
225
HRT011 Heart Septal Defect 49 1.036
226
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 0.961
227
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.961
228
PRT036 Peritonitis 65 0.961
229
ALN001 Aland Island Eye Disease 55 0.951
230
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.951
231
LPT006 Leptin Receptor Deficiency 50 0.951
232
WLF002 Wolf-Hirschhorn Syndrome 57 0.951
233
P SZR006 Seizure Disorder 70 0.898
234
SPS057 Spasticity 42 0.898
235
P HNT016 Huntington Disease 73 0.898
236
TTN003 Tetanus 65 0.898
237
OVR094 Ovarian Epithelial Cancer 39 0.898
238
THY128 Thyroid Tumor 35 0.889
239
c GLL024 Gallbladder Disease 1 52 0.889
240
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 59 0.889
241
NRN005 Neuronal Ceroid-Lipofuscinoses 61 0.889
242
HYP458 Hyper Ige Syndrome 60 0.889
243
P THR117 Three M Syndrome 1 65 0.889
244
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.889
245
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.889
246
c PRS136 Prostate Cancer, Hereditary, 6 33 0.889
247
DWN001 Down Syndrome 70 0.889
248
3MC001 3mc Syndrome 2 35 0.889
249
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 57 0.889
250
ISL014 Isolated Growth Hormone Deficiency, Type Ia 54 0.889
251
P PRS040 Prostate Cancer 95 0.889
252
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 0.889
253
c PRS130 Prostate Cancer, Hereditary, 8 32 0.889
254
LMY002 Leiomyoma 51 0.889
255
PRS047 Prostatitis 58 0.889
256
P PRS038 Personality Disorder 65 0.889
257
PNC129 Pancreatic Adenocarcinoma 65 0.889
258
CHL067 Cholecystitis 60 0.889
259
LNG031 Lung Benign Neoplasm 51 0.889
260
MYF001 Myofibroma 42 0.889
261
OST012 Osteoarthritis 77 0.889
262
NWB001 Newborn Respiratory Distress Syndrome 56 0.889
263
THY122 Thyroid Gland Cancer 59 0.889
264
FST001 Foster-Kennedy Syndrome 39 0.889
265
P ADN016 Adenocarcinoma 63 0.889
266
P GLL018 Gallbladder Cancer 53 0.889
267
3MC003 3mc Syndrome 49 0.889
268
RDN001 Reading Disorder 40 0.889
269
P CRD246 Cardiovascular System Disease 56 0.889
270
DWR001 Dwarfism 44 0.889
271
BNG077 Benign Idiopathic Neonatal Seizures 23 0.733
272
CSP005 Caspase 8 Deficiency 58 0.733
273
P PLZ001 Pelizaeus-Merzbacher Disease 65 0.733
274
CLF027 Cleft Palate, Isolated 64 0.733
275
GST092 Gastroesophageal Reflux 61 0.733
276
P PRK057 Parkinson Disease, Late-Onset 80 0.733
277
HMN044 Human Immunodeficiency Virus Type 1 78 0.733
278
INF158 Infections, Recurrent, with Encephalopathy, Hepatic Dysfunction, and Cardiovascular Malformations 30 0.733
279
RHM028 Rheumatic Heart Disease 56 0.733
281
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.733
282
P MYP004 Myopathy 67 0.733
283
P EPL164 Epilepsy 68 0.733
284
PNM008 Pneumothorax 54 0.733
285
PLM041 Pulmonary Valve Stenosis 50 0.733
286
HLX001 Helix Syndrome 48 0.733
287
ASP007 Aspiration Pneumonia 49 0.733
288
P MYG005 Myoglobinuria 40 0.733
289
PLM010 Pulmonary Edema 55 0.733
290
PLM033 Pulmonary Embolism 58 0.733
291
PTH003 Pathologic Nystagmus 52 0.733
292
BRK012 Broken Heart Syndrome 42 0.733
293
CLT003 Colitis 63 0.589
294
MBS002 Moebius Syndrome 54 0.589
295
P NRC002 Narcolepsy 56 0.589
296
ULC004 Ulcerative Colitis 74 0.589
297
CHR159 Charlie M Syndrome 21 0.589
298
SPN186 Spinal Cord Injury 61 0.518
299
P VTR007 Vitreoretinopathy 46 0.518
300
SYN031 Synovial Chondromatosis 41 0.518
301
SPS019 Spastic Paraparesis 38 0.518
302
P MYM013 Moyamoya Disease 1 59 0.518
303
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 64 0.518
304
RTN017 Retinal Detachment 60 0.518
305
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.518
306
EPD070 Epidermoid Cysts 35 0.518
307
P BRG001 Brugada Syndrome 69 0.518
308
THR099 Third-Degree Atrioventricular Block 42 0.518
309
ATR057 Atrioventricular Block 54 0.518
310
CYN002 Cyanosis, Transient Neonatal 43 0.518
311
ISC015 Ischemic Colitis 43 0.518
312
UMB002 Umbilical Hernia 47 0.518
313
CYS044 Cystic Disease of Lung 20 0.518
314
P CRD224 Cardiofaciocutaneous Syndrome 1 71 0.518
315
HLT001 Holt-Oram Syndrome 66 0.518
316
BTY001 Butyrylcholinesterase Deficiency 49 0.518
317
c HYD019 Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius 48 0.518
318
MYL057 Myelopathy, Htlv-1-Associated 38 0.518
319
c NRF024 Neurofibromatosis, Type I 72 0.518
320
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 51 0.518
321
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 53 0.518
322
GST019 Gastrointestinal Stromal Tumor 78 0.518
323
DRG024 Drug Allergy 40 0.518
324
MCL003 Macular Holes 44 0.518
325
P MSC003 Muscular Atrophy 52 0.518
326
ULN001 Ulnar Neuropathy 28 0.518
327
CLF001 Cleft Lip 53 0.518
328
STT002 Status Asthmaticus 49 0.518
329
LRN003 Learning Disability 49 0.518
330
SPN185 Spinal Cord Infarction 28 0.518
331
PST092 Posttransplant Acute Limbic Encephalitis 28 0.518
332
SYN036 Syncope 45 0.518
333
PRG001 Progressive Muscular Atrophy 41 0.518
334
PLX004 Plexopathy 29 0.518
335
ACT084 Acute Stress Disorder 54 0.518
336
NRG002 Neurogenic Bladder 55 0.518
337
P LTR001 Lateral Sclerosis 58 0.518
338
ACR007 Acromegaly 70 0.518
339
SCK001 Sick Building Syndrome 33 0.518
340
P ATR010 Atrial Heart Septal Defect 58 0.518
341
BSL004 Basilar Artery Occlusion 32 0.518
342
P MTH007 Methemoglobinemia 46 0.518
343
P HYD006 Hydrocephalus 61 0.518
344
P RHN004 Rhinitis 57 0.518
345
P PRP019 Peripheral Nervous System Disease 58 0.518
346
P PNM007 Pneumonia 67 0.518
347
LPD008 Lipid Metabolism Disorder 62 0.518
348
P MTR014 Motor Neuron Disease 65 0.518
349
WRN003 Wernicke Encephalopathy 46 0.518
350
TRP002 Tropical Spastic Paraparesis 49 0.518
351
OBS004 Obstructive Hydrocephalus 45 0.518
352
P EHL001 Ehlers-Danlos Syndrome 58 0.518
353
PST028 Post-Traumatic Stress Disorder 59 0.518
354
P RCT021 Rectum Cancer 54 0.518
355
HYP060 Hyperinsulinism 54 0.518
356
HYP706 Hypermobile Ehlers-Danlos Syndrome 55 0.518
357
P TRC031 Trichorhinophalangeal Syndrome 38 0.518
358
P NRF002 Neurofibromatosis 57 0.518
359
P HYP055 Hypoplastic Left Heart Syndrome 65 0.518
360
NRF007 Neurofibroma 64 0.518
361
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 38 0.518
362
P ENC018 Encephalopathy 62 0.518
363
DYS073 Dysphagia 53 0.518
364
P CLS010 Cluster Headache 42 0.518
366
EPD081 Epidermoid Brain Cyst 24 0.518
367
PNF002 Painful Legs and Moving Toes Syndrome 14 0.518
368
VSD002 Vas Deferens, Congenital Bilateral Aplasia of 49 0.443
369
VSD001 Vas Deferens, Congenital Bilateral Aplasia of, X-Linked 28 0.443
370
THR017 Thoracoabdominal Syndrome 40 0.443
371
P CNR004 Cone-Rod Dystrophy 2 74 0.443
372
RNL065 Renal Cell Carcinoma, Papillary, 1 79 0.443
373
ACR041 Acromelic Frontonasal Dysostosis 53 0.443
374
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.443
375
RNL114 Renal Cell Carcinoma, Nonpapillary 80 0.443
376
LNG099 Lung Disease 62 0.443
377
CMM005 Common Cold 56 0.443
378
SBP001 Subependymal Giant Cell Astrocytoma 46 0.443
379
P KDN017 Kidney Cancer 61 0.443
380
PRT035 Peritoneum Cancer 45 0.443
381
ATX019 Ataxia with Vitamin E Deficiency 44 0.443
The MalaCards human disease database index: 1-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
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