Search results for Succinylcholine

251 hits were found for Succinylcholine

# Family MCID Name MIFTS Score
1
BTY001 Butyrylcholinesterase Deficiency 50 4.067
2
SCC012 Succinylcholine Allergy 8 2.845
3
P MLG056 Malignant Hyperthermia 67 0.284
4
P CRD119 Cardiac Arrest 67 0.276
5
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.213
6
P MYP004 Myopathy 70 0.156
7
P KDN018 Kidney Disease 72 0.145
8
TTN003 Tetanus 65 0.139
9
P MYG005 Myoglobinuria 44 0.139
10
P STR020 Strabismus 55 0.127
11
MCH006 Mechanical Strabismus 42 0.127
12
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.121
13
P MSC005 Muscular Dystrophy 66 0.114
14
c ACT071 Acute Kidney Failure 60 0.114
15
HYP005 Hypokalemia 55 0.114
16
ADL002 Adult Syndrome 70 0.106
17
DPR016 Depression 63 0.106
18
MNT002 Mental Depression 58 0.106
19
OCL069 Ocular Motor Apraxia 51 0.106
20
HDN002 Head Injury 46 0.106
21
NRM005 Neuromuscular Disease 64 0.099
22
PRP016 Paraplegia 52 0.099
23
MTB004 Metabolic Acidosis 50 0.099
24
P RSP003 Respiratory Failure 74 0.090
25
ALL026 Allergic Hypersensitivity Disease 62 0.090
26
VSL002 Visual Epilepsy 59 0.090
27
P SZR006 Seizure Disorder 56 0.090
28
PNG002 Pain Agnosia 51 0.090
29
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.080
30
LPT014 Leptin Deficiency or Dysfunction 74 0.080
31
P MYS003 Myasthenia Gravis 68 0.080
32
P GLL022 Guillain-Barre Syndrome 59 0.080
33
PNM008 Pneumothorax 56 0.080
34
NRL004 Neuroleptic Malignant Syndrome 56 0.080
35
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.080
36
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.080
37
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.080
38
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.080
39
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.080
40
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.080
41
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.080
42
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.080
43
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.080
44
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.080
45
48X005 48,xyyy 39 0.080
46
MSC157 Muscular Dystrophy, Duchenne Type 72 0.070
47
CRB037 Cerebral Palsy 69 0.070
48
c RHB024 Rhabdomyosarcoma 2 67 0.070
49
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.070
50
c FNC043 Fanconi Anemia, Complementation Group E 62 0.070
51
PNM010 Pneumothorax, Primary Spontaneous 60 0.070
52
CRD223 Cardiac Arrhythmia 60 0.070
53
PHR003 Pharyngitis 57 0.070
54
INT075 Intracranial Hypertension 53 0.070
55
PRS030 Persistent Fetal Circulation Syndrome 52 0.070
56
c PRM093 Premature Ovarian Failure 7 47 0.070
57
CNT017 Central Nervous System Origin Vertigo 45 0.070
58
EST005 Esotropia 42 0.070
59
MLG086 Malignant Hyperthermia Susceptibility 39 0.070
60
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.070
61
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.070
62
MNC001 Monocular Esotropia 30 0.070
63
P ALZ034 Alzheimer Disease 88 0.057
64
STR067 Stroke, Ischemic 81 0.057
65
P RHM011 Rheumatoid Arthritis 80 0.057
66
P HRT032 Heart Disease 75 0.057
67
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.057
68
c CHR684 Chronic Kidney Disease 70 0.057
69
P ART022 Arthritis 69 0.057
70
P PNM007 Pneumonia 68 0.057
71
GST092 Gastroesophageal Reflux 67 0.057
72
CRB039 Cerebrovascular Disease 67 0.057
73
HYP056 Hypoglycemia 66 0.057
74
P MTR014 Motor Neuron Disease 65 0.057
75
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 0.057
76
MSC152 Muscular Dystrophy, Becker Type 63 0.057
77
CHN016 Cohen Syndrome 63 0.057
78
LPP008 Lipoprotein Quantitative Trait Locus 62 0.057
79
TXC005 Toxic Shock Syndrome 62 0.057
80
SPN186 Spinal Cord Injury 60 0.057
81
P CTR002 Cataract 60 0.057
82
PLM033 Pulmonary Embolism 59 0.057
83
ANR040 Aneurysm 59 0.057
84
FBR047 Fibromyalgia 58 0.057
85
EYD002 Eye Disease 58 0.057
86
P PRP019 Peripheral Nervous System Disease 58 0.057
87
P HDC001 Headache 57 0.057
88
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.057
89
P NRP001 Neuropathy 56 0.057
90
P NRF002 Neurofibromatosis 56 0.057
91
P SBS003 Substance Abuse 55 0.057
92
END040 Endogenous Depression 55 0.057
93
HMP005 Hemiplegia 55 0.057
94
PLM010 Pulmonary Edema 54 0.057
95
BRN038 Bronchial Disease 53 0.057
96
P PTS002 Ptosis 53 0.057
97
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.057
98
NRT001 Neurotic Disorder 53 0.057
99
ART140 Arteries, Anomalies of 52 0.057
100
ILS001 Ileus 51 0.057
101
ASP007 Aspiration Pneumonia 48 0.057
102
c MLG147 Malignant Hyperthermia 1 43 0.057
103
PST020 Postpoliomyelitis Syndrome 43 0.057
104
P HYP265 Hypotonia 43 0.057
105
DRG024 Drug Allergy 42 0.057
106
MYF002 Myofascial Pain Syndrome 42 0.057
107
EXT022 Exotropia 41 0.057
108
CRB086 Cerebral Aneurysms 40 0.057
109
MYT011 Myotonia 34 0.057
110
ALT003 Alternating Exotropia 34 0.057
111
PST092 Posttransplant Acute Limbic Encephalitis 29 0.057
112
c MLG150 Malignant Hyperthermia 4 21 0.057
113
PSD111 Pseudocholinesterase, Increase in Plasma Level of 5 0.057
114
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.040
115
c HYP595 Hypertension, Essential 84 0.040
116
CYS001 Cystic Fibrosis 81 0.040
117
P RTT002 Rett Syndrome 80 0.040
118
P LKM071 Leukemia, Chronic Lymphocytic 79 0.040
119
P SCH015 Schizophrenia 74 0.040
120
P OST002 Osteoporosis 74 0.040
121
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.040
122
ANX010 Anxiety 73 0.040
123
P MLT020 Multiple Sclerosis 72 0.040
124
P PHC003 Pheochromocytoma 71 0.040
125
P BRG001 Brugada Syndrome 71 0.040
126
SMT004 Smith-Lemli-Opitz Syndrome 70 0.040
127
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.040
128
P SLP006 Sleep Apnea 69 0.040
129
P LVR013 Liver Disease 68 0.040
130
P MJR001 Major Depressive Disorder 68 0.040
131
P THR014 Thrombocytopenia 67 0.040
132
PSY004 Psychotic Disorder 67 0.040
133
P TRN020 Turner Syndrome 67 0.040
134
ALC007 Alcohol Dependence 66 0.040
135
P DMN002 Dementia 66 0.040
137
CHR593 Chromosome 16p13.3 Deletion Syndrome, Proximal 66 0.040
138
P ATR011 Atrial Fibrillation 66 0.040
139
KHL003 Kohlschutter-Tonz Syndrome 65 0.040
140
c FML001 Familial Atrial Fibrillation 65 0.040
141
P ADL010 Adult Respiratory Distress Syndrome 65 0.040
142
P RHB003 Rhabdomyosarcoma 63 0.040
143
c PRC016 Pre-Eclampsia 63 0.040
144
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.040
145
P HYP069 Hyperparathyroidism 63 0.040
146
P TRC086 Trichohepatoenteric Syndrome 1 62 0.040
147
P PNC044 Pancreatitis 61 0.040
148
CNT105 Central Core Disease of Muscle 60 0.040
149
VRC005 Varicose Veins 60 0.040
150
STT001 Status Epilepticus 60 0.040
151
c OTP006 Otopalatodigital Syndrome, Type I 60 0.040
152
CHL014 Cholera 59 0.040
153
c MSC047 Muscular Dystrophy-Dystroglycanopathy , Type a, 1 59 0.040
154
IGR001 Ige Responsiveness, Atopic 59 0.040
155
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.040
156
P CNT004 Centronuclear Myopathy 59 0.040
157
PRM057 Paramyotonia Congenita of Von Eulenburg 58 0.040
158
P ALC033 Alcohol Use Disorder 58 0.040
159
c PRM005 Primary Hyperparathyroidism 58 0.040
160
CNT047 Contact Dermatitis 58 0.040
161
DSS008 Disease of Mental Health 58 0.040
162
PYR041 Pyruvate Kinase Deficiency of Red Cells 57 0.040
163
c RBN021 Rubinstein-Taybi Syndrome 1 57 0.040
164
HYP266 Hypoxia 57 0.040
165
P ANG015 Angioedema 57 0.040
166
P BPL003 Bipolar Disorder 56 0.040
167
P MYS005 Myositis 56 0.040
168
INT030 Intracranial Aneurysm 56 0.040
169
MCS002 Mucositis 56 0.040
170
P PLY019 Polyneuropathy 56 0.040
171
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.040
172
LMB062 Limb Ischemia 55 0.040
173
FDB001 Foodborne Botulism 55 0.040
174
PRP030 Purpura 54 0.040
175
AMN003 Amnestic Disorder 54 0.040
176
THR013 Thoracic Outlet Syndrome 54 0.040
177
P LTR001 Lateral Sclerosis 54 0.040
178
HLL004 Hellp Syndrome 54 0.040
179
P TRM003 Tremor 54 0.040
180
OCL006 Ocular Hypertension 53 0.040
181
CHR073 Choreatic Disease 52 0.040
182
MCN017 Meconium Ileus 52 0.040
183
ACR041 Acromelic Frontonasal Dysostosis 52 0.040
184
c ART120 Arthrogryposis, Distal, Type 3 51 0.040
185
c PNC106 Pancreatic Agenesis 1 51 0.040
186
TRM010 Traumatic Brain Injury 51 0.040
187
BHR001 Behr Syndrome 51 0.040
188
SCH012 Schizoaffective Disorder 50 0.040
189
P ECL001 Eclampsia 50 0.040
190
c SVR005 Severe Pre-Eclampsia 50 0.040
191
c ORF040 Orofaciodigital Syndrome Viii 50 0.040
192
DYS073 Dysphagia 50 0.040
193
OPT003 Opiate Dependence 50 0.040
194
47X002 47,xyy 49 0.040
195
SBP001 Subependymal Giant Cell Astrocytoma 49 0.040
196
QDR001 Quadriplegia 48 0.040
197
ATS010 Autosomal Recessive Disease 48 0.040
198
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.040
199
PNC034 Pancreas Disease 48 0.040
200
LPT006 Leptin Receptor Deficiency 48 0.040
201
OPD006 Opioid Addiction 48 0.040
202
P TRT019 Torticollis 48 0.040
203
PYL006 Pyloric Stenosis 48 0.040
204
MSC077 Muscle Eye Brain Disease 47 0.040
205
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.040
206
DRG003 Drug Dependence 47 0.040
207
P BLR006 Biliary Tract Disease 47 0.040
208
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.040
209
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.040
210
c OPT051 Opitz Gbbb Syndrome, Type I 47 0.040
211
ASP004 Asphyxia Neonatorum 46 0.040
212
ADR040 Adrenal Gland Pheochromocytoma 46 0.040
213
ANR004 Anuria 46 0.040
214
RTR001 Retrograde Amnesia 44 0.040
215
SBC016 Subacute Delirium 44 0.040
216
HPT082 Hepatic Adenomas, Familial 44 0.040
217
CVD001 Covid-19 44 0.040
218
PLY068 Polysubstance Abuse 43 0.040
219
P PRP034 Purpura Fulminans 43 0.040
220
P MJR007 Major Affective Disorder 1 43 0.040
221
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.040
222
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.040
223
c CNG513 Congenital Ptosis 42 0.040
224
FBR019 Fibromatosis 41 0.040
225
c MJR024 Major Affective Disorder 9 41 0.040
226
RDN001 Reading Disorder 40 0.040
227
ANX004 Anoxia 40 0.040
228
WND001 Wound Botulism 39 0.040
229
SPS004 Spastic Quadriplegia 39 0.040
230
ADP007 Adie Pupil 39 0.040
231
HMF008 Hemifacial Atrophy, Progressive 39 0.040
232
c MJR022 Major Affective Disorder 8 38 0.040
233
P HMF004 Hemifacial Spasm 38 0.040
234
AMP007 Amphetamine Abuse 37 0.040
235
c MJR008 Major Affective Disorder 2 35 0.040
237
c MJR023 Major Affective Disorder 7 33 0.040
238
c HMF011 Hemifacial Spasm, Familial 33 0.040
239
c MJR003 Major Affective Disorder 6 33 0.040
240
c MJR006 Major Affective Disorder 5 33 0.040
241
ACT228 Acute Radiation Syndrome 29 0.040
242
FCL003 Facial Hemiatrophy 29 0.040
243
c MJR004 Major Affective Disorder 4 28 0.040
244
c MLG151 Malignant Hyperthermia 5 28 0.040
245
HYP047 Hypertropia 27 0.040
246
HNM002 Hinman Syndrome 27 0.040
247
c MLG148 Malignant Hyperthermia 2 24 0.040
248
c MLG149 Malignant Hyperthermia 3 22 0.040
249
c MLG152 Malignant Hyperthermia 6 19 0.040
250
INH017 Inherited Congenital Spastic Tetraplegia 18 0.040
251
BLD145 Blood Group--Newfoundland 15 0.040
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