Search results for Mexiletine

187 hits were found for Mexiletine

# Family MCID Name MIFTS Score
1
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.259
2
MYT011 Myotonia 34 0.245
3
P LNG028 Long Qt Syndrome 66 0.233
4
P NRP001 Neuropathy 56 0.198
5
DBT010 Diabetic Neuropathy 54 0.188
6
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.162
7
CNG034 Congestive Heart Failure 69 0.162
8
c ACT075 Acute Myocardial Infarction 57 0.162
9
P LTR001 Lateral Sclerosis 54 0.162
10
c LNG048 Long Qt Syndrome 3 53 0.162
11
P CHR345 Chronic Pain 44 0.162
12
CRD223 Cardiac Arrhythmia 60 0.137
13
PRM057 Paramyotonia Congenita of Von Eulenburg 58 0.137
14
P MYT023 Myotonia Congenita 56 0.137
15
ISC004 Ischemia 58 0.130
16
P TRM003 Tremor 54 0.130
17
NND001 Nondystrophic Myotonia 20 0.130
18
P MYC007 Myocardial Infarction 70 0.122
19
P CRD119 Cardiac Arrest 67 0.122
20
CRD132 Cardiac Conduction Defect 58 0.122
21
ATR057 Atrioventricular Block 55 0.122
22
P ERY008 Erythromelalgia 47 0.122
23
SYN036 Syncope 45 0.122
24
P MTR014 Motor Neuron Disease 65 0.114
25
INT002 Intermittent Claudication 61 0.114
26
VSL002 Visual Epilepsy 59 0.114
27
P SZR006 Seizure Disorder 56 0.114
28
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.114
29
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.114
30
P MYT002 Myotonic Dystrophy 49 0.114
31
HDN002 Head Injury 46 0.114
32
ATX019 Ataxia with Vitamin E Deficiency 42 0.114
33
WLF001 Wolff-Parkinson-White Syndrome 66 0.106
34
SPN186 Spinal Cord Injury 60 0.106
35
P PRP019 Peripheral Nervous System Disease 58 0.106
36
P PLY019 Polyneuropathy 56 0.106
37
MYT030 Myotonia, Potassium-Aggravated 45 0.106
38
c DLT002 Dilated Cardiomyopathy 79 0.097
39
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.097
40
P CNR004 Cone-Rod Dystrophy 2 73 0.097
41
P MSC005 Muscular Dystrophy 66 0.097
42
c MCR129 Microvascular Complications of Diabetes 1 66 0.097
43
P DYS154 Dystonia 65 0.097
44
ALL026 Allergic Hypersensitivity Disease 62 0.097
45
c PNS012 Paine Syndrome 61 0.097
46
TMT001 Timothy Syndrome 61 0.097
47
c LNG047 Long Qt Syndrome 2 58 0.097
48
BRD001 Brody Myopathy 57 0.097
49
P SCK002 Sick Sinus Syndrome 55 0.097
50
c MYP132 Myopathy, Congenital 55 0.097
51
c FML191 Familial Long Qt Syndrome 53 0.097
52
DBT004 Diabetic Polyneuropathy 49 0.097
53
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.097
54
DBT002 Diabetic Autonomic Neuropathy 41 0.097
55
c MYT029 Myotonia Congenita, Autosomal Recessive 41 0.097
56
c MYT021 Myotonic Dystrophy 1 69 0.086
57
NRM005 Neuromuscular Disease 64 0.086
58
P CRN300 Coronary Heart Disease 1 63 0.086
59
P MCH002 Machado-Joseph Disease 62 0.086
60
P MYC008 Myocarditis 59 0.086
61
CNS004 Constipation 58 0.086
62
P EXN002 Exanthem 57 0.086
63
HYP005 Hypokalemia 55 0.086
64
NRM004 Neuroma 51 0.086
65
P BLP003 Blepharospasm 44 0.086
66
PRS063 Paresthesia 41 0.086
67
IMM167 Immune Deficiency Disease 78 0.075
68
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.075
69
P KDN018 Kidney Disease 72 0.075
70
HMN044 Human Immunodeficiency Virus Type 1 71 0.075
71
P BRG001 Brugada Syndrome 71 0.075
72
P EPL164 Epilepsy 71 0.075
73
P TTR001 Tetralogy of Fallot 70 0.075
74
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.075
75
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.075
76
P HYP098 Hypereosinophilic Syndrome 67 0.075
77
c RHB024 Rhabdomyosarcoma 2 67 0.075
78
P ATR011 Atrial Fibrillation 66 0.075
79
P NRV007 Nervous System Disease 66 0.075
80
IRR002 Irritable Bowel Syndrome 65 0.075
81
c NRP053 Neuropathy, Hereditary Sensory and Autonomic, Type Iia 65 0.075
82
P CHR071 Charcot-Marie-Tooth Disease 65 0.075
83
LPP008 Lipoprotein Quantitative Trait Locus 62 0.075
84
c DYS056 Dystonia 12 62 0.075
85
LVR012 Liver Cirrhosis 62 0.075
86
ACQ007 Acquired Immunodeficiency Syndrome 60 0.075
87
P CHR625 Charcot-Marie-Tooth Disease, Demyelinating, Type 1b 57 0.075
88
c MYT020 Myotonic Dystrophy 2 57 0.075
89
P CRD246 Cardiovascular System Disease 57 0.075
90
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.075
91
SNS003 Sensory Peripheral Neuropathy 54 0.075
92
ART140 Arteries, Anomalies of 52 0.075
93
PNG002 Pain Agnosia 51 0.075
94
BHR001 Behr Syndrome 51 0.075
95
DFN270 Deafness, Dystonia, and Cerebral Hypomyelination 48 0.075
96
P TRT019 Torticollis 48 0.075
97
RSS026 Roussy-Levy Hereditary Areflexic Dystasia 47 0.075
98
TTH006 Tooth Disease 46 0.075
99
P PRD021 Periodic Paralysis 45 0.075
100
P CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 44 0.075
101
CRV043 Cervical Dystonia 42 0.075
102
FCL022 Focal Dystonia 41 0.075
103
NRV004 Nerve Compression Syndrome 40 0.075
104
MTR007 Motor Peripheral Neuropathy 39 0.075
105
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.075
106
c BLP048 Blepharospasm, Benign Essential 37 0.075
107
MYT003 Myotonic Disease 35 0.075
108
DYS198 Dystonia, Focal, Task-Specific 32 0.075
109
c LNG052 Long Qt Syndrome 8 27 0.075
110
BCK007 Becker's Myotonia 10 0.075
111
P THR014 Thrombocytopenia 67 0.061
112
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.061
113
P ESP024 Esophagitis 62 0.061
114
HYP052 Hyperkalemic Periodic Paralysis 61 0.061
115
P HDC001 Headache 57 0.061
116
BRN004 Brain Edema 56 0.061
117
P MSC003 Muscular Atrophy 52 0.061
118
OCL069 Ocular Motor Apraxia 51 0.061
119
SNT005 Sinoatrial Node Disease 49 0.061
120
CRB004 Cerebral Artery Occlusion 45 0.061
121
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.061
122
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.061
123
48X005 48,xyyy 39 0.061
124
HRW001 Hair Whorl 36 0.061
125
SCN086 Scn9a Neuropathic Pain Syndromes 9 0.061
126
P HRT032 Heart Disease 75 0.043
127
P RSP003 Respiratory Failure 74 0.043
128
CRH001 Crohn's Disease 74 0.043
129
ULC004 Ulcerative Colitis 73 0.043
130
P MYP004 Myopathy 70 0.043
131
P LVR013 Liver Disease 68 0.043
132
P PNM007 Pneumonia 68 0.043
133
P HPT021 Hepatitis 67 0.043
134
ANG054 Angina Pectoris 66 0.043
135
P PLM036 Pulmonary Fibrosis 65 0.043
136
P HRP006 Herpes Simplex 65 0.043
137
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.043
138
P ERL057 Early Infantile Epileptic Encephalopathy 63 0.043
139
CLT003 Colitis 62 0.043
140
P SPN046 Spinal Muscular Atrophy 62 0.043
141
CHR619 Chromosome 2q35 Duplication Syndrome 62 0.043
142
P ORT004 Orthostatic Intolerance 62 0.043
143
DRM006 Dermatitis 61 0.043
144
P ENC018 Encephalopathy 61 0.043
145
TRG002 Trigeminal Neuralgia 60 0.043
146
LNG099 Lung Disease 60 0.043
147
STT001 Status Epilepticus 60 0.043
148
P SLP005 Sleep Disorder 59 0.043
149
GST045 Gastroenteritis 59 0.043
150
PPT005 Peptic Ulcer Disease 59 0.043
151
ERY029 Erythermalgia, Primary 58 0.043
152
FBR047 Fibromyalgia 58 0.043
153
P URT039 Urticaria 58 0.043
154
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.043
155
LNN001 Lennox-Gastaut Syndrome 57 0.043
156
P BPL003 Bipolar Disorder 56 0.043
157
P GST044 Gastritis 56 0.043
158
PRP030 Purpura 54 0.043
159
FCL014 Focal Epilepsy 54 0.043
160
HRT012 Heart Valve Disease 53 0.043
161
P FBR031 Febrile Seizures 53 0.043
162
PTH003 Pathologic Nystagmus 52 0.043
163
ILS001 Ileus 51 0.043
164
END086 End Stage Renal Disease 51 0.043
165
RDC002 Radiculopathy 50 0.043
166
P ESN008 Eosinophilic Pneumonia 50 0.043
167
SYS003 Systolic Heart Failure 49 0.043
168
47X002 47,xyy 49 0.043
169
c MTR002 Mitral Valve Insufficiency 48 0.043
170
TST044 Testicular Torsion 47 0.043
171
c SHR030 Short Qt Syndrome 46 0.043
172
CYN002 Cyanosis, Transient Neonatal 45 0.043
173
CRT015 Carotid Artery Occlusion 45 0.043
174
SPS057 Spasticity 45 0.043
175
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.043
176
c SZR007 Seizures, Benign Familial Infantile, 3 42 0.043
177
c FML294 Familial Short Qt Syndrome 41 0.043
178
c MJR024 Major Affective Disorder 9 41 0.043
179
PST053 Postherpetic Neuralgia 40 0.043
180
ANX004 Anoxia 40 0.043
181
ANG049 Angioedema Induced by Ace Inhibitors 40 0.043
182
c MJR022 Major Affective Disorder 8 38 0.043
183
P AXN001 Axonal Neuropathy 36 0.043
184
ALC011 Alcoholic Neuropathy 34 0.043
185
SNC001 Sunct Headache 29 0.043
186
CYT018 Cytochrome P450 2d6 Variant 27 0.043
187
NWD001 New Daily-Persistent Headache 21 0.043
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