Search results for Quinidine

311 hits were found for Quinidine

# Family MCID Name MIFTS Score
1
QND001 Quinidine Allergy 7 3.069
2
P ATR011 Atrial Fibrillation 66 0.396
3
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.346
4
PRP030 Purpura 55 0.267
5
SYN036 Syncope 45 0.265
6
P THR014 Thrombocytopenia 68 0.259
7
P BRG001 Brugada Syndrome 70 0.249
8
PSD088 Pseudobulbar Affect 36 0.237
9
CNG034 Congestive Heart Failure 70 0.185
10
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.182
11
P LTR001 Lateral Sclerosis 53 0.182
12
ALL026 Allergic Hypersensitivity Disease 64 0.157
13
P LPS004 Lupus Erythematosus 61 0.153
14
P MYC007 Myocardial Infarction 70 0.148
15
P CRD119 Cardiac Arrest 67 0.144
16
P LNG028 Long Qt Syndrome 65 0.139
17
P ALZ034 Alzheimer Disease 88 0.134
18
MLR004 Malaria 80 0.134
19
P HRT032 Heart Disease 75 0.134
20
P DMN002 Dementia 67 0.134
21
PLS007 Plasmodium Falciparum Malaria 52 0.134
22
c SHR030 Short Qt Syndrome 48 0.134
23
P ENC018 Encephalopathy 61 0.128
24
TRM010 Traumatic Brain Injury 53 0.128
25
CRD223 Cardiac Arrhythmia 60 0.123
26
CRD132 Cardiac Conduction Defect 59 0.123
27
DPR016 Depression 63 0.117
28
HYP005 Hypokalemia 55 0.117
29
ATR057 Atrioventricular Block 55 0.117
30
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.111
31
P EPL164 Epilepsy 71 0.111
32
P CRN018 Coronary Artery Anomaly 63 0.111
33
P NTR004 Neutropenia 63 0.111
34
DRM006 Dermatitis 61 0.111
35
P DRR001 Diarrhea 57 0.111
36
BRN071 Brain Injury 49 0.111
37
CYT018 Cytochrome P450 2d6 Variant 27 0.111
38
P MLT020 Multiple Sclerosis 72 0.105
39
c FML001 Familial Atrial Fibrillation 66 0.105
40
KHL003 Kohlschutter-Tonz Syndrome 64 0.105
41
P CRN300 Coronary Heart Disease 1 63 0.105
42
P HML002 Hemolytic Anemia 62 0.105
43
CNS004 Constipation 57 0.105
44
P EXN002 Exanthem 57 0.105
45
c ACT075 Acute Myocardial Infarction 56 0.105
46
P KDN018 Kidney Disease 70 0.098
47
P LVR013 Liver Disease 68 0.098
48
P MJR001 Major Depressive Disorder 68 0.098
49
INT002 Intermittent Claudication 61 0.098
50
MNT002 Mental Depression 57 0.098
51
P LCH002 Lichen Planus 54 0.098
52
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.098
53
ART140 Arteries, Anomalies of 53 0.098
54
c PRM092 Primary Lateral Sclerosis, Adult, 1 52 0.098
55
GRN017 Granulocytopenia 44 0.098
56
DFC004 Deficiency Anemia 75 0.091
57
c MGR028 Migraine with or Without Aura 1 69 0.091
58
WLF001 Wolff-Parkinson-White Syndrome 65 0.091
59
P TRN020 Turner Syndrome 65 0.091
60
P BRN019 Bernard-Soulier Syndrome 60 0.091
61
P SZR006 Seizure Disorder 58 0.091
62
VSL002 Visual Epilepsy 58 0.091
63
STR081 Stormorken Syndrome 57 0.091
64
P NRP001 Neuropathy 56 0.091
65
END040 Endogenous Depression 54 0.091
66
NRT001 Neurotic Disorder 52 0.091
67
ATX019 Ataxia with Vitamin E Deficiency 48 0.091
68
c FML294 Familial Short Qt Syndrome 43 0.091
70
c DLT002 Dilated Cardiomyopathy 79 0.083
71
CRB039 Cerebrovascular Disease 69 0.083
72
P HPT021 Hepatitis 67 0.083
73
PSY004 Psychotic Disorder 67 0.083
74
P CNG001 Congenital Myasthenic Syndrome 64 0.083
75
c ACT071 Acute Kidney Failure 59 0.083
76
P CRD246 Cardiovascular System Disease 56 0.083
77
DBT010 Diabetic Neuropathy 55 0.083
78
GRN009 Granulomatous Hepatitis 31 0.083
79
P SLW003 Slow-Channel Congenital Myasthenic Syndrome 31 0.083
80
P PRX010 Paroxysmal Ventricular Fibrillation 28 0.083
81
ERL052 Early Repolarization Associated with Ventricular Fibrillation 22 0.083
82
c SYS001 Systemic Lupus Erythematosus 86 0.074
83
STR067 Stroke, Ischemic 80 0.074
84
P PRK057 Parkinson Disease, Late-Onset 76 0.074
85
P SCH015 Schizophrenia 75 0.074
86
P HNT016 Huntington Disease 71 0.074
87
P MTR014 Motor Neuron Disease 64 0.074
88
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.074
89
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 62 0.074
90
P VSC011 Vasculitis 62 0.074
91
FTT001 Fatty Liver Disease 61 0.074
92
VRL011 Viral Infectious Disease 61 0.074
93
ISC004 Ischemia 60 0.074
94
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.074
95
P UVT001 Uveitis 57 0.074
96
DSS008 Disease of Mental Health 57 0.074
97
AGN016 Aging 56 0.074
98
NNL006 Non-Alcoholic Steatohepatitis 51 0.074
99
RSP002 Respiratory Syncytial Virus Infectious Disease 51 0.074
100
c BRG005 Brugada Syndrome 1 50 0.074
101
P MTR003 Mitral Valve Stenosis 50 0.074
102
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.074
103
c MYS046 Myasthenic Syndrome, Congenital, 1a, Slow-Channel 42 0.074
104
48X005 48,xyyy 39 0.074
105
P VSC018 Visceral Steatosis 33 0.074
106
c SHR031 Short Qt Syndrome 1 29 0.074
107
c ATR087 Atrial Standstill 1 74 0.064
108
DWN001 Down Syndrome 70 0.064
109
P FRN006 Frontotemporal Dementia 70 0.064
110
ADL002 Adult Syndrome 69 0.064
111
c PRG042 Progressive Familial Heart Block, Type Ia 67 0.064
112
ALC007 Alcohol Dependence 66 0.064
113
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.064
114
c MCR129 Microvascular Complications of Diabetes 1 66 0.064
115
P ATS364 Autism 65 0.064
116
P MYP004 Myopathy 64 0.064
117
LVR012 Liver Cirrhosis 63 0.064
118
c ACT068 Acute Cystitis 63 0.064
119
TRN015 Transient Cerebral Ischemia 62 0.064
120
c PNS012 Paine Syndrome 61 0.064
121
PRT058 Pure Autonomic Failure 59 0.064
122
P ALC033 Alcohol Use Disorder 58 0.064
123
CNT047 Contact Dermatitis 57 0.064
124
P HDC001 Headache 57 0.064
125
P PRP019 Peripheral Nervous System Disease 57 0.064
126
HYP266 Hypoxia 56 0.064
127
P SCK002 Sick Sinus Syndrome 55 0.064
128
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.064
129
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.064
130
RHM028 Rheumatic Heart Disease 53 0.064
131
IRD001 Iridocyclitis 50 0.064
132
P ATS011 Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 48 0.064
133
LNG015 Lingual-Facial-Buccal Dyskinesia 47 0.064
134
IMP006 Impulse Control Disorder 45 0.064
135
DBT002 Diabetic Autonomic Neuropathy 41 0.064
136
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.064
137
INT025 Intermittent Explosive Disorder 36 0.064
138
EXF003 Exfoliative Dermatitis 27 0.064
139
RCK004 Rickets 69 0.052
140
PCK003 Pick Disease of Brain 68 0.052
141
c ATS007 Autism Spectrum Disorder 67 0.052
142
HYP056 Hypoglycemia 66 0.052
143
DMN031 Dementia, Lewy Body 65 0.052
144
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 64 0.052
145
P VNW001 Von Willebrand's Disease 64 0.052
146
NRF026 Neurofibromatosis, Type Iv, of Riccardi 63 0.052
147
P GLM045 Glioma 63 0.052
148
c HPT003 Hepatitis a 63 0.052
149
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.052
150
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.052
151
ATM095 Autoimmune Disease 61 0.052
152
P PTN014 Patent Ductus Arteriosus 1 60 0.052
153
P SLP005 Sleep Disorder 59 0.052
154
P MTR012 Mitral Valve Disease 57 0.052
155
IRN002 Iron Metabolism Disease 57 0.052
156
APH002 Aphasia 57 0.052
157
VSC002 Vascular Dementia 57 0.052
158
THR024 Thrombosis 56 0.052
159
P HYP076 Hyperthyroidism 55 0.052
160
INT007 Intermediate Coronary Syndrome 55 0.052
162
PRC013 Pericarditis 54 0.052
163
HRT012 Heart Valve Disease 53 0.052
164
HMC014 Homocysteinemia 53 0.052
165
c LNG048 Long Qt Syndrome 3 52 0.052
166
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 52 0.052
167
P CHR345 Chronic Pain 50 0.052
168
AMB002 Amblyopia 50 0.052
169
VTM033 Vitamin K Deficiency Bleeding 48 0.052
170
VTM002 Vitamin B12 Deficiency 48 0.052
171
P BLD051 Blood Coagulation Disease 46 0.052
172
ANR004 Anuria 46 0.052
173
DRG013 Drug-Induced Lupus Erythematosus 46 0.052
174
GLL048 Glial Tumor 45 0.052
175
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.052
176
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.052
177
SBC016 Subacute Delirium 44 0.052
179
SPP007 Suppression Amblyopia 39 0.052
180
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.052
181
ATM052 Autoimmune Disease 1 37 0.052
182
c SHR033 Short Qt Syndrome 3 28 0.052
183
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.052
184
FRN030 Frontotemporal Dementia with Parkinsonism-17 24 0.052
185
ATR089 Atrioventricular Dissociation 20 0.052
186
P BRS047 Breast Cancer 96 0.037
187
MYL069 Myeloma, Multiple 85 0.037
188
P PNC035 Pancreatic Cancer 84 0.037
189
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.037
190
P RTN008 Retinitis Pigmentosa 77 0.037
191
P NRF023 Neurofibromatosis, Type Ii 76 0.037
192
P APL001 Aplastic Anemia 74 0.037
193
P RSP003 Respiratory Failure 74 0.037
194
c HYP836 Hypercholesterolemia, Familial, 1 72 0.037
195
P NRB001 Neuroblastoma 71 0.037
196
P SRC025 Sarcoidosis 1 70 0.037
197
P ART022 Arthritis 70 0.037
198
P HYP086 Hypothyroidism 68 0.037
199
P MYS003 Myasthenia Gravis 68 0.037
200
P PNM007 Pneumonia 68 0.037
201
P TMP003 Temporal Arteritis 67 0.037
202
c CHR684 Chronic Kidney Disease 66 0.037
203
P HYP098 Hypereosinophilic Syndrome 66 0.037
204
ANG054 Angina Pectoris 66 0.037
205
c HMP029 Hemophilia a 65 0.037
206
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.037
207
P GCH001 Gaucher's Disease 64 0.037
208
P ANR048 Aniridia 1 63 0.037
209
P NPH012 Nephrotic Syndrome 63 0.037
210
ANR007 Anorexia Nervosa 63 0.037
211
P PSR002 Psoriasis 62 0.037
212
BLL006 Bullous Pemphigoid 62 0.037
213
MDD011 Mood Disorder 62 0.037
214
P PRP029 Porphyria 62 0.037
215
P DRM010 Dermatomyositis 61 0.037
216
c BRN108 Branchiootic Syndrome 1 61 0.037
217
NRL005 Neurilemmoma 60 0.037
218
ACN002 Acanthosis Nigricans 60 0.037
219
NTH001 Netherton Syndrome 60 0.037
220
P MYL006 Myeloid Leukemia 60 0.037
221
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.037
222
WST001 West Syndrome 60 0.037
223
STT001 Status Epilepticus 59 0.037
224
P URT039 Urticaria 58 0.037
225
END030 End Stage Renal Failure 58 0.037
226
c DWL002 Dowling-Degos Disease 1 58 0.037
227
LYM027 Lymphopenia 57 0.037
228
c MST023 Mesothelioma, Malignant 57 0.037
229
LNN001 Lennox-Gastaut Syndrome 57 0.037
230
P ALP008 Alopecia 56 0.037
231
P GRV001 Graves' Disease 55 0.037
232
ALL010 Allergic Contact Dermatitis 55 0.037
233
c GRV008 Graves Disease 1 55 0.037
234
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.037
235
P VNS003 Venous Insufficiency 55 0.037
236
FCT001 Factor Viii Deficiency 55 0.037
237
PLM010 Pulmonary Edema 55 0.037
238
P ANT006 Antiphospholipid Syndrome 54 0.037
239
P ART021 Arteriosclerosis 54 0.037
240
FCL014 Focal Epilepsy 54 0.037
241
SNS003 Sensory Peripheral Neuropathy 53 0.037
242
KRT009 Keratosis 53 0.037
243
GST023 Gastric Ulcer 53 0.037
244
c FML191 Familial Long Qt Syndrome 53 0.037
245
P HMR003 Hemorrhagic Disease 52 0.037
246
PST011 Pustulosis of Palm and Sole 52 0.037
247
CHR073 Choreatic Disease 52 0.037
249
THR016 Thrombophlebitis 51 0.037
250
ILS001 Ileus 51 0.037
251
PLR008 Pleurisy 51 0.037
252
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.037
253
GSG001 Gas Gangrene 50 0.037
254
P CHL066 Cholangitis 50 0.037
255
P MGR003 Migraine with Aura 50 0.037
256
VLV047 Volvulus of Midgut 50 0.037
257
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 50 0.037
258
OPT003 Opiate Dependence 50 0.037
259
MTB004 Metabolic Acidosis 50 0.037
260
LFT001 Left Bundle Branch Hemiblock 49 0.037
261
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 49 0.037
262
BBS001 Babesiosis 48 0.037
263
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.037
264
HRD005 Hard Palate Cancer 46 0.037
265
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 46 0.037
266
RTN023 Retinitis 46 0.037
267
MYC005 Myocardial Stunning 46 0.037
268
KRT008 Keratopathy 46 0.037
269
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 46 0.037
270
P BNG032 Benign Mesothelioma 45 0.037
271
P BRB001 Beriberi 44 0.037
272
PRL008 Paralytic Ileus 44 0.037
273
DVR002 Diverticulitis 44 0.037
274
DRG024 Drug Allergy 43 0.037
275
RTT001 Ritter's Disease 43 0.037
276
SCT002 Scotoma 43 0.037
277
NRR001 Neuroretinitis 43 0.037
278
DRG002 Drug-Induced Hepatitis 42 0.037
279
RST023 Resting Heart Rate, Variation in 41 0.037
280
THR035 Thrombasthenia 41 0.037
281
UTR043 Uterine Sarcoma 40 0.037
282
MLG120 Malignant Migrating Partial Seizures of Infancy 39 0.037
283
ADP007 Adie Pupil 39 0.037
284
CTN011 Cutaneous Porphyria 38 0.037
285
ATX010 Ataxia Neuropathy Spectrum 38 0.037
286
c EPL097 Epileptic Encephalopathy, Early Infantile, 14 37 0.037
287
HPT082 Hepatic Adenomas, Familial 37 0.037
288
HMM004 Hamamy Syndrome 37 0.037
289
c HMG004 Hemoglobin D Disease 36 0.037
290
c MYS049 Myasthenic Syndrome, Congenital, 3b, Fast-Channel 36 0.037
291
SCN049 Second-Degree Atrioventricular Block 36 0.037
292
c MYS048 Myasthenic Syndrome, Congenital, 3a, Slow-Channel 34 0.037
293
RRS014 Rare Surgical Neurologic Disease 32 0.037
294
ACT064 Acute Necrotizing Encephalitis 32 0.037
295
c MYS059 Myasthenic Syndrome, Congenital, 4a, Slow-Channel 31 0.037
296
c SHR032 Short Qt Syndrome 2 30 0.037
297
HNM002 Hinman Syndrome 29 0.037
298
GRN006 Granulomatous Angiitis 29 0.037
299
c MYC058 Myocardial Infarction 2 28 0.037
300
PHT004 Photoallergic Dermatitis 28 0.037
301
P MYS047 Myasthenic Syndrome, Congenital, 1b, Fast-Channel 28 0.037
302
c MYS062 Myasthenic Syndrome, Congenital, 2a, Slow-Channel 26 0.037
303
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.037
304
c MYS060 Myasthenic Syndrome, Congenital, 4b, Fast-Channel 25 0.037
305
PLS008 Plasmodium Malariae Malaria 25 0.037
306
ANT078 Antipyrine Metabolism 24 0.037
307
c SCK022 Sick Sinus Syndrome 3 23 0.037
308
CBP002 Cebpe-Associated Autoinflammation-Immunodeficiency-Neutrophil Dysfunction Syndrome 19 0.037
309
BDR001 Bidirectional Tachycardia 19 0.037
310
BLD137 Blood Group--Ahonen 19 0.037
311
DPH028 Diaphragmatic Flutter 13 0.037
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