Search results for Halothane

305 hits were found for Halothane

# Family MCID Name MIFTS Score
1
HLT002 Halothane Hepatitis 31 6.122
2
P MLG056 Malignant Hyperthermia 60 0.541
3
P HPT021 Hepatitis 69 0.508
4
HYP266 Hypoxia 58 0.297
5
PNG002 Pain Agnosia 52 0.209
6
P CRD119 Cardiac Arrest 71 0.202
7
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.198
8
c ACT134 Acute Liver Failure 53 0.180
9
ALL026 Allergic Hypersensitivity Disease 65 0.163
10
c HPT003 Hepatitis a 60 0.163
11
DPR016 Depression 64 0.159
12
MTB004 Metabolic Acidosis 48 0.159
13
ISC004 Ischemia 62 0.154
14
MLG086 Malignant Hyperthermia Susceptibility 43 0.154
15
P LVR013 Liver Disease 71 0.145
16
STT002 Status Asthmaticus 47 0.145
17
PST092 Posttransplant Acute Limbic Encephalitis 29 0.140
18
P MYP004 Myopathy 63 0.135
19
PRT037 Pertussis 66 0.130
20
RRS014 Rare Surgical Neurologic Disease 33 0.130
21
P KDN018 Kidney Disease 73 0.124
22
ATR057 Atrioventricular Block 56 0.124
23
HLX001 Helix Syndrome 46 0.124
24
P NRB010 Neuroblastoma 1 66 0.118
25
P STR020 Strabismus 57 0.118
26
SBC016 Subacute Delirium 43 0.118
27
CRB004 Cerebral Artery Occlusion 38 0.118
28
MCH006 Mechanical Strabismus 31 0.118
29
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.106
30
P LNG028 Long Qt Syndrome 68 0.106
31
P CRN018 Coronary Artery Anomaly 67 0.106
32
P HYP098 Hypereosinophilic Syndrome 67 0.106
33
P ENC018 Encephalopathy 64 0.106
34
TTN003 Tetanus 62 0.106
35
c ACT071 Acute Kidney Failure 60 0.106
36
ART140 Arteries, Anomalies of 60 0.106
37
CRN030 Coronary Stenosis 49 0.106
38
ANX004 Anoxia 44 0.106
39
P MYG005 Myoglobinuria 43 0.106
40
P PHC003 Pheochromocytoma 71 0.099
41
c VRL010 Viral Hepatitis 56 0.099
42
P HYP076 Hyperthyroidism 55 0.099
43
ADR040 Adrenal Gland Pheochromocytoma 51 0.099
44
c MLG147 Malignant Hyperthermia 1 43 0.099
45
48X005 48,xyyy 37 0.099
46
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.099
47
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.092
48
CRD223 Cardiac Arrhythmia 61 0.092
49
CHL068 Cholestasis 61 0.092
50
P TRM003 Tremor 55 0.092
51
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 54 0.092
52
RRD056 Rare Disease in Surgical Orthopedic 29 0.092
53
DFC004 Deficiency Anemia 77 0.084
54
TXC005 Toxic Shock Syndrome 63 0.084
55
HYP066 Hyperglycemia 63 0.084
56
P CTR002 Cataract 62 0.084
57
HPT019 Hepatic Encephalopathy 60 0.084
58
HPT004 Hepatic Coma 42 0.084
59
c ATR087 Atrial Standstill 1 76 0.075
60
CNG034 Congestive Heart Failure 69 0.075
61
HYP056 Hypoglycemia 68 0.075
62
CLF027 Cleft Palate, Isolated 67 0.075
63
P GLM045 Glioma 64 0.075
64
c PRG042 Progressive Familial Heart Block, Type Ia 62 0.075
65
ATM095 Autoimmune Disease 62 0.075
66
MSL001 Measles 61 0.075
67
P SCL018 Scoliosis 61 0.075
68
P HDC001 Headache 59 0.075
69
P SCK002 Sick Sinus Syndrome 56 0.075
70
PLM010 Pulmonary Edema 56 0.075
71
AMN003 Amnestic Disorder 55 0.075
72
P HYP040 Hypospadias 54 0.075
73
BRN071 Brain Injury 51 0.075
74
47X002 47,xyy 49 0.075
75
GLL048 Glial Tumor 48 0.075
76
AST005 Asthma 80 0.065
77
P HRT032 Heart Disease 78 0.065
78
LPT014 Leptin Deficiency or Dysfunction 72 0.065
79
P HYP086 Hypothyroidism 70 0.065
80
P MSC005 Muscular Dystrophy 68 0.065
81
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.065
82
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.065
83
SPN186 Spinal Cord Injury 63 0.065
84
ING001 Inguinal Hernia 61 0.065
85
P EXN002 Exanthem 58 0.065
86
MYP139 Myopathy, Proximal, and Ophthalmoplegia 56 0.065
87
HYP005 Hypokalemia 55 0.065
88
INT075 Intracranial Hypertension 54 0.065
89
CLF001 Cleft Lip 53 0.065
90
OCL069 Ocular Motor Apraxia 53 0.065
91
CYT002 Cytokine Deficiency 46 0.065
92
CRB090 Cerebral Hypoxia 45 0.065
93
CYN002 Cyanosis, Transient Neonatal 45 0.065
94
CRT015 Carotid Artery Occlusion 44 0.065
95
SCN049 Second-Degree Atrioventricular Block 27 0.065
96
P PNC035 Pancreatic Cancer 86 0.053
97
STR067 Stroke, Ischemic 82 0.053
98
P MYC007 Myocardial Infarction 74 0.053
99
CRB039 Cerebrovascular Disease 71 0.053
100
MSC157 Muscular Dystrophy, Duchenne Type 70 0.053
101
P LYM118 Lymphoma 70 0.053
102
CRB037 Cerebral Palsy 69 0.053
103
GST092 Gastroesophageal Reflux 68 0.053
104
SRC014 Sarcoma 67 0.053
105
P HRP006 Herpes Simplex 66 0.053
106
P HML002 Hemolytic Anemia 64 0.053
107
c HPT016 Hepatitis B 63 0.053
108
LNG099 Lung Disease 62 0.053
109
RTN017 Retinal Detachment 62 0.053
110
CNT105 Central Core Disease of Muscle 61 0.053
111
P PTN014 Patent Ductus Arteriosus 1 60 0.053
112
LYM027 Lymphopenia 58 0.053
113
DSS009 Disseminated Intravascular Coagulation 58 0.053
114
INT030 Intracranial Aneurysm 57 0.053
115
SPN035 Spindle Cell Sarcoma 57 0.053
116
c SVR001 Severe Acute Respiratory Syndrome 56 0.053
117
FCL014 Focal Epilepsy 56 0.053
118
HRT012 Heart Valve Disease 56 0.053
119
P MYS005 Myositis 54 0.053
120
MSC190 Muscular Disease 54 0.053
121
QDR001 Quadriplegia 51 0.053
122
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.053
123
P RNV001 Renovascular Hypertension 49 0.053
124
HYP025 Hyperphosphatemia 47 0.053
125
PYL006 Pyloric Stenosis 47 0.053
126
ANR004 Anuria 47 0.053
127
SNT005 Sinoatrial Node Disease 46 0.053
128
ART031 Aortic Coarctation 45 0.053
129
RST023 Resting Heart Rate, Variation in 43 0.053
130
DRG002 Drug-Induced Hepatitis 41 0.053
131
SPS057 Spasticity 38 0.053
132
MYT011 Myotonia 37 0.053
133
ANT078 Antipyrine Metabolism 24 0.053
134
P CLR023 Colorectal Cancer 100 0.037
135
P ALZ034 Alzheimer Disease 90 0.037
136
c HYP595 Hypertension, Essential 87 0.037
137
P RHM011 Rheumatoid Arthritis 82 0.037
138
c DLT002 Dilated Cardiomyopathy 81 0.037
139
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.037
140
CRV035 Cervical Cancer 77 0.037
141
P NRF023 Neurofibromatosis, Type Ii 77 0.037
142
c SPN225 Spondyloarthropathy 1 74 0.037
143
P EPL164 Epilepsy 73 0.037
144
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.037
145
P TTR001 Tetralogy of Fallot 70 0.037
146
P PLM037 Pulmonary Hypertension 69 0.037
147
P MJR001 Major Depressive Disorder 69 0.037
148
P MYS003 Myasthenia Gravis 68 0.037
149
P HYP061 Hypertrophic Cardiomyopathy 68 0.037
150
ALC007 Alcohol Dependence 68 0.037
151
BRK010 Burkitt Lymphoma 68 0.037
152
MLN008 Melanoma 68 0.037
153
c JVN010 Juvenile Rheumatoid Arthritis 67 0.037
154
P ATR011 Atrial Fibrillation 67 0.037
155
BRR014 Barrett Esophagus 67 0.037
156
LVR012 Liver Cirrhosis 67 0.037
157
P MNN013 Meningitis 67 0.037
158
PRT036 Peritonitis 66 0.037
159
P BLD124 Bleeding Disorder, Platelet-Type, 11 66 0.037
160
AND002 Androgen Insensitivity Syndrome 66 0.037
161
P ANG001 Angelman Syndrome 65 0.037
162
ANR007 Anorexia Nervosa 64 0.037
163
P NTR004 Neutropenia 64 0.037
164
P ANR048 Aniridia 1 64 0.037
165
c PRC016 Pre-Eclampsia 63 0.037
166
c ATM011 Autoimmune Hepatitis 63 0.037
167
P ACR001 Aicardi-Goutieres Syndrome 63 0.037
168
FTT001 Fatty Liver Disease 63 0.037
169
NRM005 Neuromuscular Disease 62 0.037
170
ACN002 Acanthosis Nigricans 62 0.037
171
STT001 Status Epilepticus 61 0.037
172
P EPN002 Ependymoma 61 0.037
173
P VNT002 Ventricular Septal Defect 61 0.037
174
MNT002 Mental Depression 60 0.037
175
END030 End Stage Renal Failure 60 0.037
176
P GLL020 Gallbladder Disease 60 0.037
177
ADN018 Adenoma 60 0.037
178
P INF032 Infertility 60 0.037
179
P SZR006 Seizure Disorder 59 0.037
180
P BPL003 Bipolar Disorder 59 0.037
181
BRS051 Breast Disease 59 0.037
182
c ACT210 Acute Respiratory Distress Syndrome 59 0.037
183
HYP052 Hyperkalemic Periodic Paralysis 59 0.037
184
VSL002 Visual Epilepsy 58 0.037
185
CNT047 Contact Dermatitis 58 0.037
186
P AXN002 Axenfeld-Rieger Syndrome 58 0.037
187
THR024 Thrombosis 58 0.037
188
AGN016 Aging 58 0.037
189
CHL014 Cholera 58 0.037
190
TRG002 Trigeminal Neuralgia 58 0.037
191
BLR008 Bilirubin Metabolic Disorder 58 0.037
192
P TRC086 Trichohepatoenteric Syndrome 1 57 0.037
193
BCT022 Bacterial Infectious Disease 57 0.037
194
BRN004 Brain Edema 57 0.037
195
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.037
196
CMR002 Coumarin Resistance 56 0.037
197
P RTN016 Retinal Degeneration 56 0.037
198
HPT046 Hepatic Veno-Occlusive Disease 56 0.037
199
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 56 0.037
200
P NRC002 Narcolepsy 56 0.037
201
CRC006 Carcinoid Syndrome 55 0.037
202
GTR002 Goiter 54 0.037
203
PTH003 Pathologic Nystagmus 53 0.037
204
P MRN003 Marinesco-Sjogren Syndrome 53 0.037
205
P LRY019 Laryngitis 53 0.037
206
P ECL001 Eclampsia 53 0.037
207
c ACR116 Aicardi-Goutieres Syndrome 1 53 0.037
208
ALC009 Alcoholic Liver Cirrhosis 53 0.037
209
P MYT023 Myotonia Congenita 53 0.037
210
P SCK005 Sickle Cell Disease 53 0.037
211
HYP014 Hyperuricemia 52 0.037
212
OCL006 Ocular Hypertension 52 0.037
213
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 52 0.037
214
P MYT002 Myotonic Dystrophy 52 0.037
215
P OTS001 Otosclerosis 51 0.037
216
STM007 Stomatitis 51 0.037
217
ILS001 Ileus 51 0.037
218
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.037
219
c SVR005 Severe Pre-Eclampsia 50 0.037
220
P DDN001 Duodenal Ulcer 50 0.037
221
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.037
222
ACH005 Achalasia 50 0.037
223
c INF145 Infantile Liver Failure Syndrome 1 50 0.037
224
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 49 0.037
225
NTR046 Neutrophil Migration 49 0.037
226
c BCT013 Bacterial Pneumonia 49 0.037
227
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.037
228
THR013 Thoracic Outlet Syndrome 49 0.037
229
P TRM004 Trimethylaminuria 49 0.037
230
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 48 0.037
231
c BNG030 Benign Ependymoma 48 0.037
232
NRL004 Neuroleptic Malignant Syndrome 48 0.037
233
c PRG043 Progressive Familial Heart Block, Type Ib 48 0.037
234
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.037
235
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.037
236
RGH001 Right Bundle Branch Block 48 0.037
237
c EPP017 Epiphyseal Dysplasia, Multiple, 1 48 0.037
238
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.037
239
P PRD021 Periodic Paralysis 47 0.037
240
BRN014 Bronchopneumonia 47 0.037
241
c ART061 Arthrogryposis, Distal, Type 2a 47 0.037
242
PTT037 Pituitary Tumors 47 0.037
243
P MYC033 Myoclonus 47 0.037
244
HDN002 Head Injury 47 0.037
245
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.037
246
CLD007 Cold Agglutinin Disease 47 0.037
247
LFT001 Left Bundle Branch Hemiblock 47 0.037
248
c MLG069 Malignant Hypertension 46 0.037
249
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.037
250
INT067 Interstitial Nephritis 46 0.037
251
LCK001 Locked-in Syndrome 46 0.037
252
SYN036 Syncope 46 0.037
253
ASP007 Aspiration Pneumonia 46 0.037
254
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.037
255
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.037
256
NWC001 Newcastle Disease 45 0.037
257
c PRM038 Primary Agammaglobulinemia 45 0.037
258
MYC005 Myocardial Stunning 45 0.037
259
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.037
260
CLB002 Clubfoot 44 0.037
261
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.037
262
DST006 Diastolic Heart Failure 43 0.037
263
CHL109 Childhood Apraxia of Speech 43 0.037
264
c MJR024 Major Affective Disorder 9 42 0.037
265
CRB086 Cerebral Aneurysms 41 0.037
266
c TRC022 Tricuspid Valve Insufficiency 41 0.037
267
HRD005 Hard Palate Cancer 41 0.037
268
HPT082 Hepatic Adenomas, Familial 40 0.037
269
ADP007 Adie Pupil 40 0.037
270
c MJR022 Major Affective Disorder 8 39 0.037
271
ATX010 Ataxia Neuropathy Spectrum 39 0.037
272
HRN029 Hearing Loss, Noise-Induced 38 0.037
273
JJN008 Jejunoileitis 38 0.037
274
RTR001 Retrograde Amnesia 38 0.037
275
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.037
276
HRW001 Hair Whorl 36 0.037
277
c CHR682 Chronic Bilirubin Encephalopathy 36 0.037
278
ACT149 Acetaminophen Metabolism 35 0.037
279
MLG143 Malignant Hyperthermia of Anesthesia 35 0.037
280
ANT019 Anterograde Amnesia 35 0.037
281
P FML186 Familial Paroxysmal Nonkinesigenic Dyskinesia 35 0.037
282
P PLM149 Palmoplantar Keratoderma and Congenital Alopecia 2 35 0.037
283
P HYP078 Hypertrophy of Breast 35 0.037
284
SPN331 Spondyloocular Syndrome 35 0.037
285
VRT001 Vertebral Artery Occlusion 33 0.037
286
ALR002 Al-Raqad Syndrome 32 0.037
287
GRN009 Granulomatous Hepatitis 31 0.037
288
VST003 Vestibular Nystagmus 29 0.037
289
PHS025 Phosphatase, Acid, of Tissues 29 0.037
290
c MLG151 Malignant Hyperthermia 5 28 0.037
291
P ACT232 Acute Necrotizing Encephalopathy 28 0.037
292
SPL009 Splenic Sequestration 28 0.037
293
CYT018 Cytochrome P450 2d6 Variant 28 0.037
294
CHL079 Children's Interstitial Lung Disease 27 0.037
295
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 27 0.037
296
HNM002 Hinman Syndrome 26 0.037
297
AST054 Australia Antigen 25 0.037
298
MYT026 Myotonia Atrophica 25 0.037
299
c MLG150 Malignant Hyperthermia 4 21 0.037
300
DSS012 Disseminated Infection with Mycobacterium Avium Complex 21 0.037
301
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 20 0.037
302
ATR089 Atrioventricular Dissociation 20 0.037
303
ATM018 Autoimmune Disease of Urogenital Tract 19 0.037
304
BLD137 Blood Group--Ahonen 17 0.037
305
OBS524 Obsolete: Benign Exophthalmos Syndrome 13 0.037
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