Search results for Halothane

297 hits were found for Halothane

# Family MCID Name MIFTS Score
1
HLT002 Halothane Hepatitis 32 6.098
2
P MLG056 Malignant Hyperthermia 67 0.540
3
P HPT021 Hepatitis 67 0.491
4
HYP266 Hypoxia 57 0.259
5
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.198
6
PNG002 Pain Agnosia 51 0.198
7
P CRD119 Cardiac Arrest 67 0.179
8
c ACT134 Acute Liver Failure 56 0.179
9
c HPT003 Hepatitis a 62 0.163
10
ALL026 Allergic Hypersensitivity Disease 62 0.158
11
MTB004 Metabolic Acidosis 50 0.158
12
MLG086 Malignant Hyperthermia Susceptibility 39 0.154
13
P LVR013 Liver Disease 68 0.145
14
STT002 Status Asthmaticus 50 0.145
15
P MYP004 Myopathy 70 0.140
16
PST092 Posttransplant Acute Limbic Encephalitis 29 0.140
17
DPR016 Depression 63 0.135
18
PRT037 Pertussis 65 0.129
19
P KDN018 Kidney Disease 72 0.124
20
ATR057 Atrioventricular Block 55 0.124
21
HLX001 Helix Syndrome 47 0.124
22
P NRB001 Neuroblastoma 72 0.118
23
P STR020 Strabismus 55 0.118
24
CRB004 Cerebral Artery Occlusion 45 0.118
25
SBC016 Subacute Delirium 44 0.118
26
MCH006 Mechanical Strabismus 42 0.118
27
ANX004 Anoxia 40 0.112
28
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.106
29
P HYP098 Hypereosinophilic Syndrome 67 0.106
30
P LNG028 Long Qt Syndrome 66 0.106
31
TTN003 Tetanus 65 0.106
32
LPP008 Lipoprotein Quantitative Trait Locus 62 0.106
33
c ACT071 Acute Kidney Failure 60 0.106
34
ART140 Arteries, Anomalies of 52 0.106
35
CRN030 Coronary Stenosis 50 0.106
36
P MYG005 Myoglobinuria 44 0.106
37
P PHC003 Pheochromocytoma 71 0.099
38
P ENC018 Encephalopathy 61 0.099
39
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.099
40
P HYP076 Hyperthyroidism 55 0.099
41
c VRL010 Viral Hepatitis 52 0.099
42
ADR040 Adrenal Gland Pheochromocytoma 46 0.099
43
c MLG147 Malignant Hyperthermia 1 43 0.099
44
48X005 48,xyyy 39 0.099
45
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.099
46
CHL068 Cholestasis 61 0.091
47
CRD223 Cardiac Arrhythmia 60 0.091
48
P TRM003 Tremor 54 0.091
49
TXC005 Toxic Shock Syndrome 62 0.083
50
HYP066 Hyperglycemia 61 0.083
51
HPT019 Hepatic Encephalopathy 60 0.083
52
P CTR002 Cataract 60 0.083
53
ISC004 Ischemia 58 0.083
54
HPT004 Hepatic Coma 45 0.083
55
DFC004 Deficiency Anemia 70 0.075
56
CNG034 Congestive Heart Failure 69 0.075
57
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.075
58
CRB039 Cerebrovascular Disease 67 0.075
59
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.075
60
HYP056 Hypoglycemia 66 0.075
61
CLF027 Cleft Palate, Isolated 64 0.075
62
P GLM045 Glioma 63 0.075
63
ATM095 Autoimmune Disease 62 0.075
64
MSL001 Measles 62 0.075
65
P SCL018 Scoliosis 60 0.075
66
P SCK002 Sick Sinus Syndrome 55 0.075
67
AMN003 Amnestic Disorder 54 0.075
68
PLM010 Pulmonary Edema 54 0.075
69
P HYP040 Hypospadias 51 0.075
70
GLL048 Glial Tumor 45 0.075
71
STR067 Stroke, Ischemic 81 0.065
72
LPT014 Leptin Deficiency or Dysfunction 74 0.065
73
P HYP086 Hypothyroidism 69 0.065
74
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.065
75
P MSC005 Muscular Dystrophy 66 0.065
76
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.065
77
SPN186 Spinal Cord Injury 60 0.065
78
ING001 Inguinal Hernia 60 0.065
79
P EXN002 Exanthem 57 0.065
80
P HDC001 Headache 57 0.065
81
DSS009 Disseminated Intravascular Coagulation 57 0.065
82
HYP005 Hypokalemia 55 0.065
83
MYP159 Myopathy, Proximal, with Ophthalmoplegia 55 0.065
84
CLF001 Cleft Lip 53 0.065
85
INT075 Intracranial Hypertension 53 0.065
86
OCL069 Ocular Motor Apraxia 51 0.065
87
CYN002 Cyanosis, Transient Neonatal 45 0.065
88
CRT015 Carotid Artery Occlusion 45 0.065
89
CRB090 Cerebral Hypoxia 44 0.065
90
CYT002 Cytokine Deficiency 42 0.065
91
SCN049 Second-Degree Atrioventricular Block 35 0.065
92
P ALZ034 Alzheimer Disease 88 0.053
93
P PNC035 Pancreatic Cancer 84 0.053
94
AST005 Asthma 76 0.053
95
c ATR087 Atrial Standstill 1 75 0.053
96
MSC157 Muscular Dystrophy, Duchenne Type 72 0.053
97
CRB037 Cerebral Palsy 69 0.053
98
P LYM118 Lymphoma 68 0.053
99
GST092 Gastroesophageal Reflux 67 0.053
100
P HRP006 Herpes Simplex 65 0.053
101
P HML002 Hemolytic Anemia 63 0.053
102
c SVR001 Severe Acute Respiratory Syndrome 62 0.053
103
RTN017 Retinal Detachment 61 0.053
104
CNT105 Central Core Disease of Muscle 60 0.053
105
P PTN014 Patent Ductus Arteriosus 1 60 0.053
106
c HPT016 Hepatitis B 59 0.053
107
LYM027 Lymphopenia 58 0.053
108
P MYS005 Myositis 56 0.053
109
INT030 Intracranial Aneurysm 56 0.053
110
FCL014 Focal Epilepsy 54 0.053
111
HRT012 Heart Valve Disease 53 0.053
112
47X002 47,xyy 49 0.053
113
SNT005 Sinoatrial Node Disease 49 0.053
114
BRN071 Brain Injury 49 0.053
115
QDR001 Quadriplegia 48 0.053
116
P RNV001 Renovascular Hypertension 48 0.053
117
HYP025 Hyperphosphatemia 48 0.053
118
PYL006 Pyloric Stenosis 48 0.053
119
ANR004 Anuria 46 0.053
120
SPS057 Spasticity 45 0.053
121
DRG002 Drug-Induced Hepatitis 43 0.053
122
RST023 Resting Heart Rate, Variation in 41 0.053
123
MYT011 Myotonia 34 0.053
124
ANT078 Antipyrine Metabolism 24 0.053
125
P CLR023 Colorectal Cancer 99 0.037
126
c HYP595 Hypertension, Essential 84 0.037
127
c NRF023 Neurofibromatosis, Type Ii 80 0.037
128
c DLT002 Dilated Cardiomyopathy 79 0.037
129
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.037
130
CRV035 Cervical Cancer 76 0.037
131
P HRT032 Heart Disease 75 0.037
132
c SPN225 Spondyloarthropathy 1 73 0.037
133
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.037
134
P MYC007 Myocardial Infarction 70 0.037
135
P HYP061 Hypertrophic Cardiomyopathy 70 0.037
136
P TTR001 Tetralogy of Fallot 70 0.037
137
P MLN008 Melanoma 69 0.037
138
P ANG001 Angelman Syndrome 69 0.037
139
P MYS003 Myasthenia Gravis 68 0.037
140
P MJR001 Major Depressive Disorder 68 0.037
141
BRK010 Burkitt Lymphoma 67 0.037
142
P PLM037 Pulmonary Hypertension 67 0.037
143
ALC007 Alcohol Dependence 66 0.037
144
AND002 Androgen Insensitivity Syndrome 66 0.037
145
P ATR011 Atrial Fibrillation 66 0.037
146
P MNN013 Meningitis 66 0.037
147
SRC014 Sarcoma 65 0.037
148
BRR014 Barrett Esophagus 65 0.037
149
PRT036 Peritonitis 64 0.037
150
NRM005 Neuromuscular Disease 64 0.037
151
c JVN010 Juvenile Rheumatoid Arthritis 64 0.037
152
c PRC016 Pre-Eclampsia 63 0.037
153
P NTR004 Neutropenia 63 0.037
154
P ANR048 Aniridia 1 63 0.037
155
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.037
156
ANR007 Anorexia Nervosa 63 0.037
157
c ATM011 Autoimmune Hepatitis 63 0.037
158
BDD001 Budd-Chiari Syndrome 63 0.037
159
P TRC086 Trichohepatoenteric Syndrome 1 62 0.037
160
P ACR001 Aicardi-Goutieres Syndrome 62 0.037
161
LVR012 Liver Cirrhosis 62 0.037
162
FTT001 Fatty Liver Disease 61 0.037
163
HYP052 Hyperkalemic Periodic Paralysis 61 0.037
164
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 60 0.037
165
TRG002 Trigeminal Neuralgia 60 0.037
166
P BNG030 Benign Ependymoma 60 0.037
167
P VNT002 Ventricular Septal Defect 60 0.037
168
ACN002 Acanthosis Nigricans 60 0.037
169
LNG099 Lung Disease 60 0.037
170
STT001 Status Epilepticus 60 0.037
171
P AXN002 Axenfeld-Rieger Syndrome 59 0.037
172
CHL014 Cholera 59 0.037
173
VSL002 Visual Epilepsy 59 0.037
174
ADN018 Adenoma 59 0.037
175
CNT047 Contact Dermatitis 58 0.037
176
BRS051 Breast Disease 58 0.037
177
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.037
178
MNT002 Mental Depression 58 0.037
179
P INF032 Infertility 57 0.037
180
P GLL020 Gallbladder Disease 57 0.037
181
THR024 Thrombosis 57 0.037
182
c ART061 Arthrogryposis, Distal, Type 2a 57 0.037
183
BLR008 Bilirubin Metabolic Disorder 57 0.037
184
P BPL003 Bipolar Disorder 56 0.037
185
CMR002 Coumarin Resistance 56 0.037
186
HPT046 Hepatic Veno-Occlusive Disease 56 0.037
187
BCT022 Bacterial Infectious Disease 56 0.037
188
P SZR006 Seizure Disorder 56 0.037
189
NRL004 Neuroleptic Malignant Syndrome 56 0.037
190
BRN004 Brain Edema 56 0.037
191
P MYT023 Myotonia Congenita 56 0.037
192
AGN016 Aging 56 0.037
193
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 55 0.037
194
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.037
195
CRC006 Carcinoid Syndrome 55 0.037
196
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.037
197
BRN014 Bronchopneumonia 54 0.037
198
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.037
199
CLL010 Cellular Ependymoma 54 0.037
200
THR013 Thoracic Outlet Syndrome 54 0.037
201
P RTN016 Retinal Degeneration 53 0.037
202
OCL006 Ocular Hypertension 53 0.037
203
GTR002 Goiter 53 0.037
204
SPN035 Spindle Cell Sarcoma 53 0.037
205
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.037
206
P LRY019 Laryngitis 52 0.037
207
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.037
208
P DDN001 Duodenal Ulcer 52 0.037
209
c ACR116 Aicardi-Goutieres Syndrome 1 52 0.037
210
P NRC002 Narcolepsy 52 0.037
211
PTH003 Pathologic Nystagmus 52 0.037
212
HYP014 Hyperuricemia 52 0.037
213
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.037
214
ILS001 Ileus 51 0.037
215
CLB002 Clubfoot 51 0.037
216
ACH005 Achalasia 51 0.037
217
END086 End Stage Renal Disease 51 0.037
218
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.037
219
P ECL001 Eclampsia 50 0.037
220
c SVR005 Severe Pre-Eclampsia 50 0.037
221
STM007 Stomatitis 50 0.037
222
P SCK005 Sickle Cell Disease 50 0.037
223
c INF145 Infantile Liver Failure Syndrome 1 50 0.037
224
NTR046 Neutrophil Migration 50 0.037
225
P OTS001 Otosclerosis 49 0.037
226
P MYT002 Myotonic Dystrophy 49 0.037
227
LFT001 Left Bundle Branch Hemiblock 49 0.037
228
c BCT013 Bacterial Pneumonia 48 0.037
229
ASP007 Aspiration Pneumonia 48 0.037
230
RGH001 Right Bundle Branch Block 48 0.037
231
INT067 Interstitial Nephritis 48 0.037
232
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.037
233
c MLG069 Malignant Hypertension 47 0.037
234
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.037
235
P CRC039 Coarctation of Aorta 47 0.037
236
MYC005 Myocardial Stunning 46 0.037
237
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.037
238
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.037
239
P MYC033 Myoclonus 46 0.037
240
HDN002 Head Injury 46 0.037
241
SYN036 Syncope 45 0.037
242
c TRC022 Tricuspid Valve Insufficiency 45 0.037
243
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.037
244
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.037
245
NWC001 Newcastle Disease 45 0.037
246
DST006 Diastolic Heart Failure 45 0.037
247
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.037
248
P PRD021 Periodic Paralysis 45 0.037
249
CLD007 Cold Agglutinin Disease 45 0.037
250
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.037
251
RTR001 Retrograde Amnesia 44 0.037
252
PTT037 Pituitary Tumors 44 0.037
253
P PLM149 Palmoplantar Keratoderma and Congenital Alopecia 2 44 0.037
254
c PRM038 Primary Agammaglobulinemia 44 0.037
255
HPT082 Hepatic Adenomas, Familial 44 0.037
256
CHL109 Childhood Apraxia of Speech 44 0.037
257
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.037
258
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.037
259
P HYP078 Hypertrophy of Breast 43 0.037
260
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.037
261
c MJR024 Major Affective Disorder 9 41 0.037
262
ISL151 Isolated Elevated Serum Creatine Phosphokinase Levels 40 0.037
263
CRB086 Cerebral Aneurysms 40 0.037
264
HYP344 Hyperthyroidism, Familial Gestational 39 0.037
265
ADP007 Adie Pupil 39 0.037
266
c CHR682 Chronic Bilirubin Encephalopathy 39 0.037
267
ANT019 Anterograde Amnesia 38 0.037
268
c MJR022 Major Affective Disorder 8 38 0.037
269
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.037
270
HRN029 Hearing Loss, Noise-Induced 37 0.037
271
P FML186 Familial Paroxysmal Nonkinesigenic Dyskinesia 37 0.037
272
SPN331 Spondyloocular Syndrome 36 0.037
273
HRW001 Hair Whorl 36 0.037
274
SPL009 Splenic Sequestration 35 0.037
275
ACT149 Acetaminophen Metabolism 35 0.037
276
ATX010 Ataxia Neuropathy Spectrum 34 0.037
277
ALR002 Al-Raqad Syndrome 33 0.037
278
ACT064 Acute Necrotizing Encephalitis 33 0.037
279
GRN009 Granulomatous Hepatitis 33 0.037
280
JJN008 Jejunoileitis 31 0.037
281
SPP004 Suppurative Cholangitis 30 0.037
282
VRT001 Vertebral Artery Occlusion 30 0.037
283
MTY003 Mutyh Polyposis 30 0.037
284
c MLG151 Malignant Hyperthermia 5 28 0.037
285
PHS025 Phosphatase, Acid, of Tissues 28 0.037
286
HNM002 Hinman Syndrome 27 0.037
287
CYT018 Cytochrome P450 2d6 Variant 27 0.037
288
CHL079 Children's Interstitial Lung Disease 26 0.037
289
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.037
290
AST054 Australia Antigen 26 0.037
291
VST003 Vestibular Nystagmus 25 0.037
292
TRM026 Trimethoprim Allergy 22 0.037
293
c MLG150 Malignant Hyperthermia 4 21 0.037
294
ATR089 Atrioventricular Dissociation 20 0.037
295
DSS012 Disseminated Infection with Mycobacterium Avium Complex 20 0.037
296
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 19 0.037
297
BLD137 Blood Group--Ahonen 16 0.037
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