The MalaCard for "arrhythmia" has been retired.
Searching MalaCards for entries containing "arrhythmia"

346 hits were found for 'arrhythmia'

# ++ Fam MCID Name MIFTS Score
1
PHC009 Phocomelia Ectrodactyly Deafness Sinus Arrhythmia 12 4.544
2
SDD004 Sudden Arrhythmia Death Syndrome 15 3.294
3
PHC010 Phocomelia-Ectrodactyly Ear Malformation Deafness and Sinus Arrhythmia 3 3.220
4
CRD054 Cardiac Arrhythmia, Ankyrin-B-Related 4 3.118
5
SDD005 Sudden Cardiac Death Multi-Gene Panels 19 2.645
6
c CRD152 Cardiomyopathy, Familial Hypertrophic, 21 15 2.411
7
WLF001 Wolff-Parkinson-White Syndrome 60 2.371
8
OGD001 Ogden Syndrome 14 2.205
9
c LNG057 Long Qt Syndrome 13 17 0.268
10
P MYC007 Myocardial Infarction 82 0.196
11
P SPL033 Split-Hand/foot Malformation 6 33 0.168
12
c LNG056 Long Qt Syndrome 12 17 0.164
13
c ACT075 Acute Myocardial Infarction 59 0.152
14
c BRG001 Brugada Syndrome 55 0.143
15
c CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 50 0.143
16
P DLT002 Dilated Cardiomyopathy 74 0.139
17
c SPL037 Split Hand Foot Malformation 33 0.134
18
CNG288 Congenital Absence of Upper Arm and Forearm with Hand Present 10 0.134
19
P MTR005 Mitral Valve Prolapse 54 0.129
20
c SCK002 Sick Sinus Syndrome 50 0.129
21
AND003 Andersen-Tawil Syndrome 39 0.129
22
CRD132 Cardiac Conduction Defect 32 0.119
23
MCR033 Macrocephaly-Capillary Malformation 13 0.119
24
c SRC013 Sarcoidosis 60 0.113
25
c HYP061 Hypertrophic Cardiomyopathy 59 0.113
26
HYP005 Hypokalemia 50 0.113
27
SYN036 Syncope 49 0.113
28
ISC004 Ischemia 57 0.107
29
c MYT002 Myotonic Dystrophy 49 0.107
30
CRD003 Cardiac Sarcoidosis 46 0.107
31
NSY001 N Syndrome 57 0.101
32
P LNG044 Long Qt Syndrome 1 53 0.101
33
P MYC008 Myocarditis 51 0.101
34
c LNG047 Long Qt Syndrome 2 31 0.101
35
CNG034 Congestive Heart Failure 74 0.095
36
c LNG053 Long Qt Syndrome 9 32 0.095
37
DBT010 Diabetic Neuropathy 59 0.088
38
NRP001 Neuropathy 54 0.088
39
c ATN004 Autonomic Neuropathy 52 0.088
40
DBT002 Diabetic Autonomic Neuropathy 44 0.088
41
ATR055 Atrial Septal Aneurysm 20 0.088
42
ANK002 Ankylosing Spondylitis 75 0.080
43
c MSC005 Muscular Dystrophy 54 0.080
44
c HYP051 Hypokalemic Periodic Paralysis 53 0.080
45
HYP006 Hypertensive Heart Disease 51 0.080
46
MGL022 Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome, Somatic 23 0.080
47
P SDD001 Sudden Infant Death Syndrome 65 0.072
48
P SYS005 Systemic Scleroderma 63 0.072
49
CRD137 Cardiogenic Shock 56 0.072
50
THR013 Thoracic Outlet Syndrome 53 0.072
51
SYS003 Systolic Heart Failure 48 0.072
52
P JRV001 Jervell-Lange Nielsen Syndrome 47 0.072
53
INF013 Inferior Myocardial Infarction 37 0.072
54
CTS011 Cutis Marmorata Telangiectatica Congenita 37 0.072
55
P HYP075 Hypertension 76 0.062
56
CRN211 Coronary Artery Disease, 68 0.062
57
SPS077 Sepsis 67 0.062
58
c HYP076 Hyperthyroidism 55 0.062
59
P TMT001 Timothy Syndrome 48 0.062
60
c LFT003 Left Ventricular Noncompaction 48 0.062
61
c LNG028 Long Qt Syndrome 47 0.062
62
CRN030 Coronary Stenosis 47 0.062
63
c ACT076 Acute Myocarditis 47 0.062
64
ATR057 Atrioventricular Block 43 0.062
65
c THY054 Thyrotoxic Periodic Paralysis 40 0.062
66
GNT019 Giant Cell Myocarditis 33 0.062
67
SPN148 Spondylometaphyseal Dysplasia Sedaghatian Type 16 0.062
68
MRF001 Marfan Syndrome 78 0.051
69
P WSK001 Wiskott-Aldrich Syndrome 76 0.051
70
ACR007 Acromegaly 75 0.051
71
P RFS001 Refsum Disease 73 0.051
72
CST001 Costello Syndrome 71 0.051
73
DCH001 Duchenne Muscular Dystrophy 70 0.051
74
SPN186 Spinal Cord Injury 63 0.051
75
PLY041 Polymyositis 61 0.051
76
c SPN046 Spinal Muscular Atrophy 60 0.051
77
P RSP003 Respiratory Failure 60 0.051
78
CHG001 Chagas Disease 58 0.051
79
SLP006 Sleep Apnea 57 0.051
80
P FML032 Familial Hypertrophic Cardiomyopathy 56 0.051
81
CND002 Conduct Disorder 56 0.051
82
MYC002 Mycobacterium Avium Complex Disease 56 0.051
83
PTN001 Patent Foramen Ovale 56 0.051
84
c EMR001 Emery-Dreifuss Muscular Dystrophy 56 0.051
85
SNS001 Sensorineural Hearing Loss 55 0.051
86
HYP037 Hyperhomocysteinemia 55 0.051
87
BRT005 Barth Syndrome 54 0.051
88
P PLY019 Polyneuropathy 54 0.051
89
c SCL016 Scleroderma 53 0.051
90
HYP017 Hypophosphatemia 52 0.051
91
P ATN005 Autonomic Dysfunction 52 0.051
92
c FCL014 Focal Epilepsy 52 0.051
93
CCN002 Cocaine Abuse 52 0.051
94
P MSC003 Muscular Atrophy 51 0.051
95
ADL002 Adult Syndrome 50 0.051
96
OBS006 Obstructive Lung Disease 49 0.051
97
PHC013 Phaeochromocytoma 48 0.051
98
PRC012 Pericardial Effusion 47 0.051
99
MYC005 Myocardial Stunning 46 0.051
100
c DXT001 Dextrocardia 45 0.051
101
ARR001 Arrhythmogenic Right Ventricular Dysplasia 43 0.051
102
TKT001 Tako-Tsubo Cardiomyopathy 42 0.051
103
CHR101 Char Syndrome 42 0.051
104
c MCR103 Microtia 40 0.051
105
CRN041 Carnitine-Acylcarnitine Translocase Deficiency 39 0.051
106
PRP009 Peripartum Cardiomyopathy 39 0.051
107
c HYP052 Hyperkalemic Periodic Paralysis 39 0.051
108
STR037 Stress Cardiomyopathy 37 0.051
109
c SHR030 Short Qt Syndrome 33 0.051
110
GST007 Gastric Dilatation 33 0.051
111
P PRX010 Paroxysmal Ventricular Fibrillation 26 0.051
112
HSB001 His Bundle Tachycardia 18 0.051
113
c LNG048 Long Qt Syndrome 3 15 0.051
114
c LNG050 Long Qt Syndrome 5 14 0.051
115
c LNG051 Long Qt Syndrome 6 13 0.051
116
c LNG046 Long Qt Syndrome 11 12 0.051
117
c LNG049 Long Qt Syndrome 4 12 0.051
118
c VNT013 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1 10 0.051
119
P AST005 Asthma 86 0.036
120
P TBR001 Tuberous Sclerosis 81 0.036
121
CDS001 Cadasil 80 0.036
122
P BPL003 Bipolar Disorder 76 0.036
123
P RTT002 Rett Syndrome 75 0.036
124
AND002 Androgen Insensitivity Syndrome 75 0.036
125
FBR012 Fabry Disease 74 0.036
126
P PRM021 Primary Pulmonary Hypertension 74 0.036
127
P HMC003 Hemochromatosis 73 0.036
128
ANX002 Anxiety Disorder 73 0.036
129
PRP027 Peripheral Vascular Disease 71 0.036
130
ATH003 Atherosclerosis 69 0.036
131
KWS002 Kawasaki Disease 69 0.036
132
VSC007 Vascular Disease 69 0.036
133
P CNG006 Congenital Hypothyroidism 69 0.036
134
HYP004 Hypercalcemia 69 0.036
135
ASP006 Aspergillosis 68 0.036
136
THY014 Thyroid Medullary Carcinoma 68 0.036
137
P WGN002 Wegener's Granulomatosis 67 0.036
138
P ANG001 Angelman Syndrome 67 0.036
139
P PRM005 Primary Hyperparathyroidism 66 0.036
140
ACT033 Acute Intermittent Porphyria 66 0.036
141
HYP056 Hypoglycemia 66 0.036
142
P AMY004 Amyloidosis 65 0.036
143
P SYS004 Systemic Mastocytosis 65 0.036
144
c HYP095 Hypercholesterolemia 65 0.036
145
c LCL006 Localized Scleroderma 64 0.036
146
P TMP003 Temporal Arteritis 64 0.036
147
c ESS002 Essential Hypertension 64 0.036
148
ART019 Aortic Valve Stenosis 64 0.036
149
WST001 West Syndrome 64 0.036
150
VNH001 Von Hippel-Lindau Disease 63 0.036
151
ART021 Arteriosclerosis 63 0.036
152
ISC006 Ischemic Heart Disease 62 0.036
153
PLY017 Polyarteritis Nodosa 62 0.036
154
LYM017 Lyme Disease 62 0.036
155
c MNN013 Meningitis 62 0.036
156
P MTH008 Methylmalonic Acidemia 62 0.036
157
PTN002 Patent Ductus Arteriosus 61 0.036
158
P MGR002 Migraine 61 0.036
159
BRN106 Burns 61 0.036
160
HYP266 Hypoxia 60 0.036
161
RHM001 Rheumatic Fever 60 0.036
162
BRN029 Brain Disease 60 0.036
163
PRP001 Propionic Acidemia 60 0.036
164
TYP007 Typhoid Fever 60 0.036
165
P DRM010 Dermatomyositis 59 0.036
166
P CNG030 Congenital Muscular Dystrophy 59 0.036
167
P MJR001 Major Depressive Disorder 58 0.036
168
MCR088 Microscopic Polyangiitis 58 0.036
169
P GLY008 Glycogen Storage Disease Ii 57 0.036
170
c HYP069 Hyperparathyroidism 57 0.036
171
c AXN002 Axenfeld-Rieger Syndrome 57 0.036
172
P NNN008 Noonan Syndrome 1 56 0.036
173
P SHR029 Short Syndrome 55 0.036
174
c LMB006 Limb-Girdle Muscular Dystrophy 55 0.036
175
c CNG042 Congenital Central Hypoventilation Syndrome 55 0.036
176
THY033 Thyrotoxicosis 55 0.036
177
P HYP055 Hypoplastic Left Heart Syndrome 55 0.036
178
CRN017 Coronary Thrombosis 55 0.036
179
TRN015 Transient Cerebral Ischemia 55 0.036
180
c SYP003 Syphilis 55 0.036
181
DDN006 Duodenitis 54 0.036
182
GLL031 Guillain-Barr´┐Ż Syndrome 54 0.036
183
SCN006 Secondary Syphilis 53 0.036
184
LPD010 Lipodystrophy 53 0.036
185
SPR004 Supravalvular Aortic Stenosis 53 0.036
186
YLL002 Yellow Fever 53 0.036
187
LDD002 Liddle Syndrome 52 0.036
188
c MYP004 Myopathy 52 0.036
189
STT002 Status Asthmaticus 52 0.036
190
c CNT035 Central Nervous System Disease 52 0.036
191
FBR047 Fibromyalgia 52 0.036
192
CRD001 Cardiac Tamponade 51 0.036
193
ART004 Aortic Atherosclerosis 51 0.036
194
BTL001 Botulism 51 0.036
195
P NRV007 Nervous System Disease 51 0.036
196
CNN005 Connective Tissue Disease 51 0.036
197
SNG010 Single Median Maxillary Central Incisor 50 0.036
198
MTN003 Motion Sickness 50 0.036
199
c CNG018 Congenital Heart Block 50 0.036
200
P MLS001 Melas Syndrome 50 0.036
201
EPD037 Epidermal Nevus 49 0.036
202
P CTN014 Cutaneous Mastocytosis 49 0.036
203
c PSD015 Pseudohypoparathyroidism 49 0.036
204
ANH002 Anhidrosis 48 0.036
205
TRY001 Trypanosomiasis 48 0.036
206
c MTR012 Mitral Valve Disease 48 0.036
207
P BRT004 Bartter Disease 48 0.036
208
INV001 Invasive Aspergillosis 47 0.036
209
PNN001 Panniculitis 47 0.036
210
LGN002 Legionellosis 47 0.036
211
IMP005 Impotence 47 0.036
212
EBS001 Ebstein Anomaly 47 0.036
213
c GLY007 Glycogen Storage Disease Iv 47 0.036
214
HMR004 Hemorrhagic Fever with Renal Syndrome 46 0.036
215
P HTR003 Heterotaxy 46 0.036
216
P FCS001 Facioscapulohumeral Muscular Dystrophy 46 0.036
217
CRN029 Coronary Arteriosclerosis 45 0.036
218
P HYP192 Hypocalcemia, Autosomal Dominant 45 0.036
219
c SMP003 Simpson-Golabi-Behmel Syndrome 45 0.036
220
AGR002 Agoraphobia 45 0.036
221
INF034 Infective Endocarditis 44 0.036
222
ESN011 Eisenmenger Syndrome 44 0.036
223
EHL034 Ehlers-Danlos Syndrome, Hypermobility Type 44 0.036
224
P OCL013 Oculodentodigital Dysplasia 44 0.036
225
c CNT048 Central Hypoventilation Syndrome 44 0.036
226
FCL012 Facial Paralysis 44 0.036
227
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 44 0.036
228
ALC010 Alcoholic Cardiomyopathy 44 0.036
229
P MYF003 Myofibrillar Myopathy 43 0.036
230
RLY001 Riley-Day Syndrome 43 0.036
231
c FML058 Familial Dilated Cardiomyopathy 43 0.036
232
P END033 Endocarditis 42 0.036
233
HRT012 Heart Valve Disease 42 0.036
234
CRN055 Carney Triad 42 0.036
235
c CNG012 Congenital Generalized Lipodystrophy 42 0.036
236
CNG045 Congenital Dyserythropoietic Anemia Type I 41 0.036
237
c BPL002 Bipolar I Disorder 41 0.036
238
P STC005 Stickler Syndrome Type 1 41 0.036
239
CNT015 Central Sleep Apnea 41 0.036
240
NXS001 Naxos Disease 41 0.036
241
c RST002 Restrictive Cardiomyopathy 41 0.036
242
TRN012 Transient Global Amnesia 40 0.036
243
END021 Endomyocardial Fibrosis 40 0.036
244
ATX019 Ataxia with Vitamin E Deficiency 40 0.036
245
HYP022 Hypohidrosis 40 0.036
246
c LPR012 Leopard Syndrome 1 39 0.036
247
CNG219 Congenital Aural Atresia 39 0.036
248
AGG002 Aggressive Systemic Mastocytosis 39 0.036
249
P VNT028 Ventricular Septal Defect 1 38 0.036
250
FTT003 Fatty Acid Oxidation Disorders 38 0.036
251
DXR001 Doxorubicin Induced Cardiomyopathy 38 0.036
252
AMY038 Amyloidosis, Renal 37 0.036
253
P KLF001 Kleefstra Syndrome 37 0.036
254
c MYT007 Myotonic Dystrophy Type 2 36 0.036
255
P LYM029 Lymphedema-Distichiasis Syndrome 36 0.036
256
TRC062 Tricuspid Atresia 36 0.036
257
DMN023 Diamond-Blackfan Anemia 1 36 0.036
258
P HRT021 Heart Block, Progressive, Type Ia 35 0.036
259
P PRX064 Peroxisome Biogenesis Disorder 2b 35 0.036
260
P HYP216 Hypoparathyroidism Familial Isolated 35 0.036
261
EFM001 Efemp2-Related Cutis Laxa 35 0.036
262
MTR046 Maternally Inherited Diabetes and Deafness 35 0.036
263
YNG002 Young Syndrome 34 0.036
264
P MLG090 Malignant Hyperthermia Susceptibility Type 1 34 0.036
265
c ADL016 Adult Spinal Muscular Atrophy 34 0.036
266
PLM068 Pulmonary Vein Stenosis 34 0.036
267
BRN055 Bronchogenic Cyst 33 0.036
268
CHL028 Childhood Type Dermatomyositis 33 0.036
269
P SYS007 Systemic Capillary Leak Syndrome 32 0.036
270
c FML162 Familial Mediterranean Fever, Ad 32 0.036
271
P VNT010 Ventricular Tachycardia, Catecholaminergic Polymorphic, 2 31 0.036
272
MNN032 Meningococcal Meningitis 31 0.036
273
MTC028 Mitochondrial Cardiomyopathy 31 0.036
274
DPH006 Diaphragmatic Eventration 30 0.036
275
DVC001 Devic Disease 29 0.036
276
SCH035 Schwartz Jampel Syndrome Type 1 29 0.036
277
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 29 0.036
278
GLS004 Glossopharyngeal Neuralgia 29 0.036
279
ART007 Aorta Atresia 26 0.036
280
CNG225 Congenital Dyserythropoietic Anemia Type 2 26 0.036
281
SBS006 Sebastian Syndrome 25 0.036
282
MYP007 Myopathy Due to Cpt Ii Deficiency 25 0.036
283
HRT006 Heart Aneurysm 24 0.036
284
PRN037 Prinzmetal's Variant Angina 24 0.036
285
P HYP239 Hyperkalemic Periodic Paralysis Type 2 23 0.036
286
APL022 Aplasia Cutis Congenita, Reticulolinear, with Mmicrocephaly, Facial Dysmorphism and Other Congenital Anomalies 23 0.036
287
ANT054 Anotia 23 0.036
288
LWN001 Lown-Ganong-Levine Syndrome 23 0.036
289
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 22 0.036
290
c HMC021 Hemochromatosis, Type 2a 21 0.036
291
IMG001 Image Syndrome 20 0.036
292
LFT001 Left Bundle Branch Hemiblock 20 0.036
293
HYP203 Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extrapyramidal Syndrome 20 0.036
294
FDB001 Foodborne Botulism 19 0.036
295
P 19P001 19p13.12 Microdeletion Syndrome 19 0.036
296
TRT006 Torticollis Keloids Cryptorchidism Renal Dysplasia 19 0.036
297
AND005 Androgen Insensitivity Syndrome, Mild 19 0.036
298
P BSL014 Basilar Migraine 18 0.036
299
CPL011 Capillary Malformations, Congenital, 1, Somatic, Mosaic 18 0.036
300
c SDD002 Sudden Infant Death with Dysgenesis of the Testes Syndrome 17 0.036
301
CPT003 Cpt Deficiency, Hepatic, Type Ia 17 0.036
302
PGD001 Pagod Syndrome 17 0.036
303
c BNG076 Benign Exophthalmos Syndrome 17 0.036
304
SHP003 Shapiro Syndrome 17 0.036
305
ATM069 Autoimmune Hemolytic Anemia, Warm Type 16 0.036
306
PCW002 Pcwh Syndrome 16 0.036
307
BRC019 Brachycephalofrontonasal Dysplasia 16 0.036
308
MXD035 Mixed-Type Autoimmune Hemolytic Anemia 16 0.036
309
INT062 Interstitial Myocarditis 16 0.036
310
XLN031 X-Linked Visceral Heterotaxy 1 15 0.036
311
EHL044 Ehlers-Danlos Syndrome, Autosomal Recessive, Due to Tenascin X Deficiency 15 0.036
312
16P006 16p11.2p12.2 Microdeletion Syndrome 15 0.036
313
SNG003 Single Ventricular Heart 15 0.036
314
MLT129 Multifocal Atrial Tachycardia 14 0.036
315
TBT001 Tabatznik Syndrome 14 0.036
316
P MCL055 Mcleod Syndrome with or Without Chronic Granulomatous Disease 14 0.036
317
MTC068 Mitochondrial Complex V Deficiency, Nuclear Type 2 14 0.036
318
TXC010 Toxic Myocarditis 14 0.036
319
CPT005 Cpt Ii Deficiency, Lethal Neonatal 14 0.036
320
DFN007 Deafness Enamel Hypoplasia Nail Defects 14 0.036
321
c EMR004 Emery-Dreifuss Muscular Dystrophy, X-Linked 14 0.036
322
PLY088 Polyvalvular Heart Disease Syndrome 14 0.036
323
CPT004 Cpt Deficiency, Hepatic, Type Ii 13 0.036
324
DMD003 Dmd-Associated Dilated Cardiomyopathy 13 0.036
325
NTH002 Nathalie Syndrome 13 0.036
326
c VNT026 Ventricular Septal Defect 2 13 0.036
327
DRG014 Drug-Induced Autoimmune Hemolytic Anemia 12 0.036
328
WLL009 Woolly Hair Hypotrichosis Everted Lower Lip and Outstanding Ears 12 0.036
329
SBN001 Subendocardial Myocardial Infarction 12 0.036
330
BDR001 Bidirectional Tachycardia 11 0.036
331
HRS003 Hirschsprung Disease Ganglioneuroblastoma 11 0.036
332
DGT004 Digitalis Poisoning 11 0.036
333
SBR006 Subaortic Stenosis Short Stature Syndrome 11 0.036
334
c VNT024 Ventricular Septal Defect 3 11 0.036
335
ECT023 Ectodermal Dysplasia, Hidrotic, Christianson-Fourie Type 10 0.036
336
FML092 Familial Ventricular Tachycardia 10 0.036
337
RBB001 Ribbing Disease 10 0.036
338
EXT038 Extrasystoles Short Stature Hyperpigmentation Microcephaly 9 0.036
339
CV3005 Cav3-Related Sudden Infant Death Syndrome 9 0.036
340
c FML196 Familial Isolated Hypoparathyroidism Due to Agenesis of Parathyroid Gland 9 0.036
341
CRD023 Cardiomyopathy Cataract Hip Spine Disease 8 0.036
342
PLY042 Polyneuropathy Mental Retardation Acromicria Premature Menopause 7 0.036
343
CRN208 Coronary Sinus Atresia 7 0.036
344
MSC030 Muscular Fibrosis Multifocal Obstructed Vessels 6 0.036
345
c CRD154 Cardiomyopathy, Familial Hypertrophic 6 5 0.036
346
c EMR003 Emery-Dreifuss Muscular Dystrophy, Dominant Type 2 0.036