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Search results for Enflurane

269 hits were found for Enflurane

# Family MCID Name MIFTS Score
1
P ANR048 Aniridia 1 66 2.612
2
HLT002 Halothane Hepatitis 32 2.363
3
P PHC003 Pheochromocytoma 70 2.270
4
ADR040 Adrenal Gland Pheochromocytoma 45 2.270
5
P MLG056 Malignant Hyperthermia 65 2.270
6
PNG002 Pain Agnosia 51 2.233
7
AMN003 Amnestic Disorder 53 2.128
8
STT002 Status Asthmaticus 49 2.120
9
TTN003 Tetanus 64 1.955
10
P SZR006 Seizure Disorder 69 1.883
11
MTB004 Metabolic Acidosis 48 1.679
12
P SCL018 Scoliosis 57 1.600
13
ATR057 Atrioventricular Block 54 1.560
14
P MYC033 Myoclonus 46 1.414
15
P PRP029 Porphyria 60 1.400
16
P SCK002 Sick Sinus Syndrome 55 1.382
17
P HYP040 Hypospadias 51 1.382
18
SNT005 Sinoatrial Node Disease 48 1.365
19
P HYP076 Hyperthyroidism 53 1.355
20
ANX004 Anoxia 40 1.346
21
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 1.320
22
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 1.320
23
ATR089 Atrioventricular Dissociation 21 1.307
24
PRP083 Porphyria, Acute Intermittent 64 1.285
25
HRT012 Heart Valve Disease 53 1.263
26
CLF027 Cleft Palate, Isolated 64 1.239
27
c HPT003 Hepatitis a 63 1.185
28
c ACT071 Acute Kidney Failure 60 1.119
29
CHL068 Cholestasis 61 1.119
30
ILS001 Ileus 49 1.085
31
P MYG005 Myoglobinuria 40 1.078
32
P KDN018 Kidney Disease 71 1.078
33
VLK001 Volkmann Contracture 23 1.045
34
c HYP595 Hypertension, Essential 84 1.024
35
LPP008 Lipoprotein Quantitative Trait Locus 65 1.001
36
ACT078 Acute Porphyria 50 1.001
37
RTN020 Retinal Vascular Disease 45 1.001
38
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.977
39
INT075 Intracranial Hypertension 52 0.977
40
HDN002 Head Injury 44 0.977
41
P HDC001 Headache 56 0.977
42
PHT008 Photosensitive Epilepsy 41 0.952
43
MYC080 Myoclonic Epilepsy of Unverricht and Lundborg 52 0.952
44
P STR020 Strabismus 56 0.952
45
P TMP001 Temporal Lobe Epilepsy 49 0.952
46
BRN014 Bronchopneumonia 52 0.952
47
ERL001 Early Myoclonic Encephalopathy 62 0.952
48
MCH006 Mechanical Strabismus 40 0.952
49
ANT078 Antipyrine Metabolism 24 0.924
50
c PRG042 Progressive Familial Heart Block, Type Ia 65 0.924
51
P RNV001 Renovascular Hypertension 48 0.924
52
c VRL010 Viral Hepatitis 52 0.924
53
GLM045 Glioma 62 0.924
54
GLL048 Glial Tumor 51 0.924
55
SCN049 Second-Degree Atrioventricular Block 34 0.893
56
GST092 Gastroesophageal Reflux 59 0.893
57
CRV035 Cervical Cancer 72 0.893
58
P ECL001 Eclampsia 52 0.893
59
QDR001 Quadriplegia 49 0.893
60
c PRC016 Pre-Eclampsia 64 0.893
61
MSL001 Measles 61 0.893
62
SPS057 Spasticity 43 0.893
63
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.858
64
INT030 Intracranial Aneurysm 55 0.858
65
P HPT021 Hepatitis 68 0.858
66
P GLM007 Glomerulonephritis 59 0.858
67
CRN030 Coronary Stenosis 50 0.858
68
c SVR005 Severe Pre-Eclampsia 49 0.858
69
ALD013 Aldosterone-Producing Adenoma 36 0.858
70
CRB086 Cerebral Aneurysms 40 0.858
71
P HMR005 Hemorrhoid 49 0.840
72
DRG002 Drug-Induced Hepatitis 42 0.816
73
CNS004 Constipation 56 0.816
74
GLC003 Glucose Intolerance 53 0.816
75
PRC013 Pericarditis 53 0.816
76
PTT037 Pituitary Tumors 44 0.816
77
IMP016 Impacted Teeth, Multiple 8 0.762
78
P TRT019 Torticollis 47 0.762
79
P MYS003 Myasthenia Gravis 67 0.762
80
P ALC033 Alcohol Use Disorder 67 0.762
81
STT001 Status Epilepticus 58 0.762
82
ALC006 Alcoholic Hepatitis 61 0.762
83
P CTR002 Cataract 59 0.762
84
P MTR012 Mitral Valve Disease 57 0.762
85
RTN017 Retinal Detachment 60 0.631
86
ARG002 Argininosuccinic Aciduria 61 0.631
87
ANS021 Anisocoria 24 0.631
88
P MTR014 Motor Neuron Disease 65 0.631
89
P GLL022 Guillain-Barre Syndrome 59 0.631
90
P MSC005 Muscular Dystrophy 66 0.631
91
EXP004 Exophthalmos 50 0.631
92
MYT011 Myotonia 37 0.631
93
HLX001 Helix Syndrome 47 0.370
94
WLF001 Wolff-Parkinson-White Syndrome 63 0.346
95
ALL029 Allergic Disease 61 0.346
96
PNM008 Pneumothorax 54 0.321
97
MYM001 Myoma 54 0.321
98
P CYS018 Cystitis 58 0.293
99
P NRB001 Neuroblastoma 66 0.293
100
MLG086 Malignant Hyperthermia Susceptibility 40 0.293
101
BRT054 Brittle Bone Disorder 74 0.262
102
EPL050 Epilepsy, Partial, with Pericentral Spikes 26 0.262
103
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.262
104
P PRP019 Peripheral Nervous System Disease 57 0.262
105
ART074 Aortic Dissection 53 0.262
106
CYT002 Cytokine Deficiency 43 0.262
107
P NRP001 Neuropathy 59 0.262
108
HPT019 Hepatic Encephalopathy 59 0.227
109
LVR012 Liver Cirrhosis 62 0.227
110
ASP008 Aspiration Pneumonitis 43 0.227
111
ART016 Aortic Aneurysm 68 0.227
112
TXC005 Toxic Shock Syndrome 61 0.227
113
ALC009 Alcoholic Liver Cirrhosis 54 0.227
114
CHL013 Cholecystolithiasis 37 0.227
115
HPT004 Hepatic Coma 43 0.227
116
PLM033 Pulmonary Embolism 58 0.227
117
CRB090 Cerebral Hypoxia 42 0.227
118
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.185
119
VRC005 Varicose Veins 59 0.185
120
OTT002 Otitis Media 70 0.185
121
PNM010 Pneumothorax, Primary Spontaneous 58 0.185
122
P PRP003 Porphyria Cutanea Tarda 66 0.185
123
HND015 Hand Skill, Relative 29 0.185
124
CRD223 Cardiac Arrhythmia 63 0.185
125
SCK003 Sickle Cell Anemia 74 0.185
126
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.185
127
ESP021 Esophageal Cancer 84 0.185
128
MTN003 Motion Sickness 50 0.185
129
c ACT249 Acute Asthma 40 0.185
130
PRP030 Purpura 54 0.185
131
P ATR010 Atrial Heart Septal Defect 58 0.185
132
CRB037 Cerebral Palsy 66 0.185
133
HRT011 Heart Septal Defect 49 0.185
134
P URN019 Urinary Tract Infection 48 0.185
135
RTR001 Retrograde Amnesia 41 0.185
136
P LVR013 Liver Disease 68 0.185
137
THR016 Thrombophlebitis 50 0.185
138
GTR002 Goiter 52 0.185
139
RGH001 Right Bundle Branch Block 47 0.185
140
PLM041 Pulmonary Valve Stenosis 50 0.185
141
GST040 Gastric Adenocarcinoma 66 0.185
142
P MYT002 Myotonic Dystrophy 51 0.185
143
SBC016 Subacute Delirium 42 0.185
144
INT007 Intermediate Coronary Syndrome 53 0.185
145
P SCK005 Sickle Cell Disease 56 0.185
146
48X005 48,xyyy 39 0.185
147
c BCT013 Bacterial Pneumonia 47 0.185
148
P TRM003 Tremor 50 0.185
149
P CHR345 Chronic Pain 50 0.185
150
c ACT134 Acute Liver Failure 57 0.185
151
IDP070 Idiopathic Scoliosis 41 0.131
152
PHN011 Phenytoin Toxicity 32 0.131
153
P CRN300 Coronary Heart Disease 1 73 0.131
154
P CRD119 Cardiac Arrest 68 0.131
155
P PRG013 Paraganglioma 57 0.131
156
P SLP006 Sleep Apnea 69 0.131
157
KRT010 Kartagener Syndrome 49 0.131
158
ASP007 Aspiration Pneumonia 49 0.131
159
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.131
160
ART140 Arteries, Anomalies of 52 0.131
161
c LNG044 Long Qt Syndrome 1 66 0.131
162
FBR011 Fibrodysplasia Ossificans Progressiva 67 0.131
163
c SCL052 Scleroderma, Familial Progressive 60 0.131
164
P SCL057 Scoliosis, Isolated 1 40 0.131
165
OCL069 Ocular Motor Apraxia 57 0.131
166
c GLC092 Glaucoma, Primary Open Angle 60 0.131
167
P HRS035 Hirschsprung Disease 1 66 0.131
168
P BRN019 Bernard-Soulier Syndrome 61 0.131
169
P BLD134 Bladder Cancer 79 0.131
170
INT017 Intestinal Schistosomiasis 51 0.131
171
ATS010 Autosomal Recessive Disease 42 0.131
172
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.131
173
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.131
174
CYN002 Cyanosis, Transient Neonatal 43 0.131
175
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 0.131
176
c THY107 Thymoma, Familial 42 0.131
177
c CRD065 Cardiomyopathy, Familial Hypertrophic, 2 48 0.131
178
P STS008 Sotos Syndrome 1 62 0.131
179
P MYM013 Moyamoya Disease 1 59 0.131
180
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.131
181
APN008 Apnea, Obstructive Sleep 66 0.131
182
THY111 Thyroid Carcinoma, Familial Medullary 67 0.131
183
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.131
184
c MLG147 Malignant Hyperthermia 1 47 0.131
185
PCT003 Pectus Excavatum 43 0.131
186
P DST002 Distal Arthrogryposis 63 0.131
187
TBS001 Tabes Dorsalis 30 0.131
188
P RSP003 Respiratory Failure 73 0.131
189
ESP002 Esophageal Varix 51 0.131
190
DSS009 Disseminated Intravascular Coagulation 56 0.131
191
MLG157 Malignant Pheochromocytoma 37 0.131
192
CRD001 Cardiac Tamponade 44 0.131
193
ASY002 Asymptomatic Neurosyphilis 41 0.131
194
P VNT002 Ventricular Septal Defect 58 0.131
195
P ART021 Arteriosclerosis 53 0.131
196
P HMR003 Hemorrhagic Disease 59 0.131
197
P ESS003 Essential Thrombocythemia 68 0.131
198
P THY023 Thymoma 64 0.131
199
P STR021 Struma Ovarii 39 0.131
200
SCK001 Sick Building Syndrome 33 0.131
201
P LNG028 Long Qt Syndrome 63 0.131
202
P HMN010 Hemangioma 61 0.131
203
NRM004 Neuroma 49 0.131
204
P TBR001 Tuberous Sclerosis 69 0.131
205
P HRN001 Horner's Syndrome 45 0.131
206
P MLT074 Multiple Endocrine Neoplasia 58 0.131
207
ISC004 Ischemia 61 0.131
208
PRP016 Paraplegia 52 0.131
209
HPT014 Hepatorenal Syndrome 49 0.131
210
GST037 Gastroparesis 52 0.131
211
P OBS001 Obstructive Jaundice 49 0.131
212
PLC009 Placenta Praevia 39 0.131
213
P SYS005 Systemic Scleroderma 73 0.131
214
P MYP004 Myopathy 67 0.131
215
P SYP003 Syphilis 59 0.131
216
PLC005 Placental Insufficiency 55 0.131
217
P PLM036 Pulmonary Fibrosis 65 0.131
218
THY125 Thyroid Gland Medullary Carcinoma 48 0.131
219
P PNC044 Pancreatitis 61 0.131
220
c ACT027 Acute Pancreatitis 60 0.131
221
P HYP061 Hypertrophic Cardiomyopathy 68 0.131
222
P ADL010 Adult Respiratory Distress Syndrome 70 0.131
223
ATN004 Autonomic Neuropathy 42 0.131
224
CLB002 Clubfoot 50 0.131
225
P OPN001 Open-Angle Glaucoma 55 0.131
226
PRT013 Portal Hypertension 59 0.131
227
THY001 Thyroid Crisis 30 0.131
228
P HYD006 Hydrocephalus 62 0.131
229
P ART005 Arteriovenous Malformation 64 0.131
230
c MLG069 Malignant Hypertension 46 0.131
231
P THR005 Thrombotic Thrombocytopenic Purpura 64 0.131
232
SCH014 Schistosomiasis 56 0.131
233
TRN012 Transient Global Amnesia 38 0.131
234
HYD002 Hydronephrosis 58 0.131
235
PRT037 Pertussis 49 0.131
236
CHL004 Cholelithiasis 48 0.131
237
P DRM010 Dermatomyositis 61 0.131
238
HLL004 Hellp Syndrome 53 0.131
239
P CWD010 Cowden Syndrome 70 0.131
240
BRN024 Bronchitis 67 0.131
241
ADR008 Adrenal Adenoma 55 0.131
242
P CMP008 Compartment Syndrome 49 0.131
243
P OVR046 Ovarian Cyst 43 0.131
244
BP1002 Bap1 Tumor Predisposition Syndrome 42 0.131
245
P NRC002 Narcolepsy 55 0.131
246
P BRN022 Bronchiectasis 59 0.131
247
DXT001 Dextrocardia 54 0.131
248
SKN019 Skin Melanoma 70 0.131
249
HPT009 Hepatopulmonary Syndrome 48 0.131
250
P BLR006 Biliary Tract Disease 46 0.131
251
BLR012 Biliary Hypoplasia 11 0.131
252
STS002 Situs Inversus 44 0.131
253
NRS003 Neurosyphilis 45 0.131
254
MCP033 Mucopolysaccharidoses 44 0.131
255
ATN005 Autonomic Dysfunction 45 0.131
256
CRC006 Carcinoid Syndrome 55 0.131
257
MYC005 Myocardial Stunning 45 0.131
258
PNF002 Painful Legs and Moving Toes Syndrome 14 0.131
259
GGN002 Gigantism 32 0.131
260
SYN036 Syncope 44 0.131
261
TRM010 Traumatic Brain Injury 50 0.131
262
CRR012 Cirrhotic Cardiomyopathy 22 0.131
263
CCN009 Cocaine Intoxication 30 0.131
264
CNG506 Congenital Amyoplasia 27 0.131
265
SPL018 Splenomegaly 47 0.131
266
DYS073 Dysphagia 53 0.131
267
CRB087 Cerebral Arteriosclerosis 17 0.131
268
HYP266 Hypoxia 56 0.131
269
THY029 Thyroid Carcinoma 55 0.131
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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