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

313 hits were found for 'arrhythmia'

# Family MCID Name MIFTS Score
1
PHC009 Phocomelia Ectrodactyly Deafness Sinus Arrhythmia 19 4.552
2
PHC010 Phocomelia-Ectrodactyly Ear Malformation Deafness and Sinus Arrhythmia 4 3.225
3
SDD004 Sudden Arrhythmia Death Syndrome 11 3.212
4
CRD054 Cardiac Arrhythmia, Ankyrin-B-Related 7 3.120
5
SDD005 Sudden Cardiac Death Multi-Gene Panels 21 2.526
6
WLF001 Wolff-Parkinson-White Syndrome 65 2.379
7
c CRD152 Cardiomyopathy, Familial Hypertrophic, 21 17 2.342
8
OGD001 Ogden Syndrome 19 2.206
9
P MYC007 Myocardial Infarction 88 0.217
10
c LNG028 Long Qt Syndrome 61 0.200
11
P SPL033 Split-Hand/foot Malformation 6 36 0.174
12
c ACT075 Acute Myocardial Infarction 61 0.166
13
c BRG001 Brugada Syndrome 56 0.149
14
c CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 51 0.149
15
P DLT002 Dilated Cardiomyopathy 82 0.144
16
c SCK002 Sick Sinus Syndrome 52 0.139
17
c SPL037 Split Hand Foot Malformation 25 0.139
18
CNG288 Congenital Absence of Upper Arm and Forearm with Hand Present 14 0.139
19
ARR001 Arrhythmogenic Right Ventricular Dysplasia 59 0.134
20
P MTR005 Mitral Valve Prolapse 55 0.134
21
AND003 Andersen-Tawil Syndrome 43 0.129
22
P HYP075 Hypertension 86 0.123
23
c SRC013 Sarcoidosis 69 0.118
24
c HYP061 Hypertrophic Cardiomyopathy 61 0.118
25
HYP005 Hypokalemia 50 0.118
26
P CRD132 Cardiac Conduction Defect 27 0.118
27
ISC004 Ischemia 64 0.112
28
c MYT002 Myotonic Dystrophy 54 0.112
29
CRD003 Cardiac Sarcoidosis 49 0.112
30
P MYC008 Myocarditis 56 0.105
31
CNG034 Congestive Heart Failure 81 0.098
32
TTR001 Tetralogy of Fallot 76 0.098
33
DBT010 Diabetic Neuropathy 68 0.091
34
NRP001 Neuropathy 61 0.091
35
c ATN004 Autonomic Neuropathy 54 0.091
36
DBT002 Diabetic Autonomic Neuropathy 48 0.091
37
ANK002 Ankylosing Spondylitis 75 0.083
38
P MYT006 Myotonic Dystrophy Type 1 67 0.083
39
P LNG044 Long Qt Syndrome 1 66 0.083
40
c MSC005 Muscular Dystrophy 62 0.083
41
HYP006 Hypertensive Heart Disease 56 0.083
42
c HYP051 Hypokalemic Periodic Paralysis 56 0.083
43
SCN006 Secondary Syphilis 55 0.083
44
P SYS005 Systemic Scleroderma 69 0.074
45
P JRV001 Jervell-Lange Nielsen Syndrome 54 0.074
46
SYS003 Systolic Heart Failure 51 0.074
47
INF013 Inferior Myocardial Infarction 38 0.074
48
CRN211 Coronary Artery Disease 72 0.064
49
P SDD001 Sudden Infant Death Syndrome 70 0.064
50
c HYP076 Hyperthyroidism 61 0.064
51
CRB009 Cerebritis 56 0.064
52
P TMT001 Timothy Syndrome 53 0.064
53
CRN030 Coronary Stenosis 53 0.064
54
c ACT076 Acute Myocarditis 49 0.064
55
ATR057 Atrioventricular Block 44 0.064
56
c SHR030 Short Qt Syndrome 41 0.064
57
P RFS001 Refsum Disease 83 0.053
58
ACR007 Acromegaly 80 0.053
59
CST001 Costello Syndrome 79 0.053
60
DCH001 Duchenne Muscular Dystrophy 78 0.053
61
P RSP003 Respiratory Failure 70 0.053
62
P FML032 Familial Hypertrophic Cardiomyopathy 69 0.053
63
CHG001 Chagas Disease 66 0.053
64
P PLY019 Polyneuropathy 64 0.053
65
c SPN046 Spinal Muscular Atrophy 63 0.053
66
BRT005 Barth Syndrome 62 0.053
67
PTN001 Patent Foramen Ovale 60 0.053
68
CND002 Conduct Disorder 59 0.053
69
c SCL016 Scleroderma 59 0.053
70
OBS006 Obstructive Lung Disease 57 0.053
71
FCL014 Focal Epilepsy 57 0.053
72
MYC002 Mycobacterium Avium Complex Disease 57 0.053
73
SNS001 Sensorineural Hearing Loss 56 0.053
74
HYP037 Hyperhomocysteinemia 55 0.053
75
PRC012 Pericardial Effusion 54 0.053
76
c EMR001 Emery-Dreifuss Muscular Dystrophy 53 0.053
77
HYP017 Hypophosphatemia 53 0.053
78
CCN002 Cocaine Abuse 53 0.053
79
ADL002 Adult Syndrome 52 0.053
80
P MSC003 Muscular Atrophy 52 0.053
81
PHC013 Phaeochromocytoma 49 0.053
82
MYC005 Myocardial Stunning 49 0.053
83
DXT001 Dextrocardia 48 0.053
84
c MYT007 Myotonic Dystrophy Type 2 48 0.053
85
PRP009 Peripartum Cardiomyopathy 42 0.053
86
CRN041 Carnitine-Acylcarnitine Translocase Deficiency 42 0.053
87
c HYP052 Hyperkalemic Periodic Paralysis 41 0.053
88
c LNG047 Long Qt Syndrome 2 40 0.053
89
MCR103 Microtia 39 0.053
90
c LNG053 Long Qt Syndrome 9 35 0.053
91
GST007 Gastric Dilatation 34 0.053
92
RGH001 Right Bundle Branch Block 34 0.053
93
c LNG048 Long Qt Syndrome 3 23 0.053
94
c LNG056 Long Qt Syndrome 12 20 0.053
95
c LNG050 Long Qt Syndrome 5 19 0.053
96
c LNG051 Long Qt Syndrome 6 19 0.053
97
c LNG057 Long Qt Syndrome 13 19 0.053
98
HSB001 His Bundle Tachycardia 18 0.053
99
c VNT013 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1 17 0.053
100
c LNG049 Long Qt Syndrome 4 16 0.053
101
c LNG046 Long Qt Syndrome 11 13 0.053
102
CDS001 Cadasil 92 0.037
103
MRF001 Marfan Syndrome 92 0.037
104
P TBR001 Tuberous Sclerosis 91 0.037
105
VNH001 Von Hippel-Lindau Disease 89 0.037
106
FBR012 Fabry Disease 88 0.037
107
AND002 Androgen Insensitivity Syndrome 88 0.037
108
P WSK001 Wiskott-Aldrich Syndrome 87 0.037
109
P HNT001 Huntington's Disease 87 0.037
110
P RTT002 Rett Syndrome 85 0.037
111
P PRM021 Primary Pulmonary Hypertension 82 0.037
112
P THY014 Thyroid Medullary Carcinoma 81 0.037
113
P BPL003 Bipolar Disorder 80 0.037
114
P HMC003 Hemochromatosis 80 0.037
115
P MTH008 Methylmalonic Acidemia 79 0.037
116
ACT033 Acute Intermittent Porphyria 78 0.037
117
ANX002 Anxiety Disorder 75 0.037
118
P WGN002 Wegener's Granulomatosis 75 0.037
119
PRP027 Peripheral Vascular Disease 75 0.037
120
KWS002 Kawasaki Disease 74 0.037
121
P GLY008 Glycogen Storage Disease Ii 73 0.037
122
ASP006 Aspergillosis 73 0.037
123
P CNG030 Congenital Muscular Dystrophy 72 0.037
124
VSC007 Vascular Disease 72 0.037
125
P PRM005 Primary Hyperparathyroidism 72 0.037
126
c CNG006 Congenital Hypothyroidism 72 0.037
127
c ESS002 Essential Hypertension 71 0.037
128
c MNN013 Meningitis 71 0.037
129
ATH003 Atherosclerosis 71 0.037
130
P MGR002 Migraine 71 0.037
131
P DRM010 Dermatomyositis 70 0.037
132
P SYS004 Systemic Mastocytosis 70 0.037
133
P ANG001 Angelman Syndrome 70 0.037
134
P TMP003 Temporal Arteritis 69 0.037
135
P PRP001 Propionic Acidemia 69 0.037
136
HYP004 Hypercalcemia 69 0.037
137
ISC006 Ischemic Heart Disease 69 0.037
138
P NNN008 Noonan Syndrome 1 69 0.037
139
ART019 Aortic Valve Stenosis 68 0.037
140
c LCL006 Localized Scleroderma 68 0.037
141
PLY017 Polyarteritis Nodosa 68 0.037
142
LYM017 Lyme Disease 67 0.037
143
HYP056 Hypoglycemia 66 0.037
144
P AMY004 Amyloidosis 65 0.037
145
ART021 Arteriosclerosis 65 0.037
146
PTN002 Patent Ductus Arteriosus 65 0.037
147
RHM001 Rheumatic Fever 65 0.037
148
HMR004 Hemorrhagic Fever with Renal Syndrome 65 0.037
149
WST001 West Syndrome 64 0.037
150
BRN106 Burns 64 0.037
151
NRN002 Neuronitis 64 0.037
152
c GLY007 Glycogen Storage Disease Iv 64 0.037
153
c HYP069 Hyperparathyroidism 63 0.037
154
TYP007 Typhoid Fever 63 0.037
155
DDN006 Duodenitis 62 0.037
156
TNS005 Tonsillitis 62 0.037
157
BRN029 Brain Disease 62 0.037
158
P MLS001 Melas Syndrome 61 0.037
159
P CNG042 Congenital Central Hypoventilation Syndrome 61 0.037
160
P NRV007 Nervous System Disease 61 0.037
161
ADN002 Adenoiditis 60 0.037
162
c AXN002 Axenfeld-Rieger Syndrome 60 0.037
163
P LDD002 Liddle Syndrome 60 0.037
164
c CNT035 Central Nervous System Disease 60 0.037
165
LPD010 Lipodystrophy 59 0.037
166
P MJR001 Major Depressive Disorder 58 0.037
167
CTN014 Cutaneous Mastocytosis 58 0.037
168
THY033 Thyrotoxicosis 58 0.037
169
P MYP004 Myopathy 58 0.037
170
RLY001 Riley-Day Syndrome 58 0.037
171
YLL002 Yellow Fever 57 0.037
172
SNG010 Single Median Maxillary Central Incisor 57 0.037
173
STT002 Status Asthmaticus 57 0.037
174
c LMB006 Limb-Girdle Muscular Dystrophy 57 0.037
175
CNN005 Connective Tissue Disease 57 0.037
176
CRN017 Coronary Thrombosis 57 0.037
177
MTN003 Motion Sickness 57 0.037
178
DRG003 Drug Dependence 57 0.037
179
P SYP003 Syphilis 56 0.037
180
P HYP055 Hypoplastic Left Heart Syndrome 56 0.037
181
P MTR012 Mitral Valve Disease 56 0.037
182
c PSD015 Pseudohypoparathyroidism 55 0.037
183
ATX019 Ataxia with Vitamin E Deficiency 55 0.037
184
SPR004 Supravalvular Aortic Stenosis 55 0.037
185
TRN015 Transient Cerebral Ischemia 55 0.037
186
BTL001 Botulism 55 0.037
187
LGN002 Legionellosis 55 0.037
188
ART004 Aortic Atherosclerosis 54 0.037
189
PLY041 Polymyositis 54 0.037
190
THR013 Thoracic Outlet Syndrome 54 0.037
191
MCR088 Microscopic Polyangiitis 53 0.037
192
PNN001 Panniculitis 53 0.037
193
P STC005 Stickler Syndrome Type 1 53 0.037
194
CRN029 Coronary Arteriosclerosis 53 0.037
195
P HYP192 Hypocalcemia, Autosomal Dominant 52 0.037
196
c CNG018 Congenital Heart Block 52 0.037
197
P CRV039 Cervicitis 52 0.037
198
EHL034 Ehlers-Danlos Syndrome, Hypermobility Type 52 0.037
199
IMP005 Impotence 52 0.037
200
CRD001 Cardiac Tamponade 52 0.037
201
P LPR012 Leopard Syndrome 1 52 0.037
202
END030 End Stage Renal Failure 52 0.037
203
EBS001 Ebstein Anomaly 52 0.037
204
ANH002 Anhidrosis 52 0.037
205
P CNG045 Congenital Dyserythropoietic Anemia Type I 50 0.037
206
TRY001 Trypanosomiasis 50 0.037
207
INF034 Infective Endocarditis 50 0.037
208
c BRT004 Bartter Disease 49 0.037
209
P OCL013 Oculodentodigital Dysplasia 49 0.037
210
INV001 Invasive Aspergillosis 49 0.037
211
FCL012 Facial Paralysis 49 0.037
212
ALC010 Alcoholic Cardiomyopathy 48 0.037
213
P END033 Endocarditis 48 0.037
214
P FCS001 Facioscapulohumeral Muscular Dystrophy 47 0.037
215
AGG002 Aggressive Systemic Mastocytosis 47 0.037
216
c MYF003 Myofibrillar Myopathy 47 0.037
217
c RST002 Restrictive Cardiomyopathy 47 0.037
218
P DMN023 Diamond-Blackfan Anemia 1 47 0.037
219
P MLG090 Malignant Hyperthermia Susceptibility Type 1 47 0.037
220
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 46 0.037
221
HRT012 Heart Valve Disease 46 0.037
222
AGR002 Agoraphobia 46 0.037
223
P PRX064 Peroxisome Biogenesis Disorder 2b 45 0.037
224
MTR046 Maternally Inherited Diabetes and Deafness 45 0.037
225
c CNG012 Congenital Generalized Lipodystrophy 44 0.037
226
LYM029 Lymphedema-Distichiasis Syndrome 44 0.037
227
P HRT021 Heart Block, Progressive, Type Ia 44 0.037
228
P HYP216 Hypoparathyroidism Familial Isolated 43 0.037
229
P KLF001 Kleefstra Syndrome 42 0.037
230
P CNT015 Central Sleep Apnea 42 0.037
231
END021 Endomyocardial Fibrosis 42 0.037
232
TRN012 Transient Global Amnesia 42 0.037
233
SYN053 Syndromic Diarrhea 42 0.037
234
HYP022 Hypohidrosis 41 0.037
235
CRN055 Carney Triad 41 0.037
236
CHL028 Childhood Type Dermatomyositis 40 0.037
237
NXS001 Naxos Disease 40 0.037
238
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 39 0.037
239
c ADL016 Adult Spinal Muscular Atrophy 39 0.037
240
SCH035 Schwartz Jampel Syndrome Type 1 38 0.037
241
MYP007 Myopathy Due to Cpt Ii Deficiency 37 0.037
242
c FML162 Familial Mediterranean Fever, Ad 37 0.037
243
P VNT010 Ventricular Tachycardia, Catecholaminergic Polymorphic, 2 36 0.037
244
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 34 0.037
245
c CNG225 Congenital Dyserythropoietic Anemia Type 2 34 0.037
246
TKT001 Tako-Tsubo Cardiomyopathy 34 0.037
247
P HYP239 Hyperkalemic Periodic Paralysis Type 2 34 0.037
248
MGL023 Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome, Somatic 33 0.037
249
c CTS030 Cutis Laxa, Autosomal Recessive, Type Ia 31 0.037
250
c HMC021 Hemochromatosis, Type 2a 31 0.037
251
P VNT028 Ventricular Septal Defect 1 31 0.037
252
c THY054 Thyrotoxic Periodic Paralysis 31 0.037
253
GLS004 Glossopharyngeal Neuralgia 31 0.037
254
APL022 Aplasia Cutis Congenita, Reticulolinear, with Mmicrocephaly, Facial Dysmorphism and Other Congenital Anomalies 30 0.037
255
DPH006 Diaphragmatic Eventration 29 0.037
256
SBS006 Sebastian Syndrome 28 0.037
257
PCW002 Pcwh Syndrome 27 0.037
258
ART007 Aorta Atresia 27 0.037
259
STR037 Stress Cardiomyopathy 27 0.037
260
HRT006 Heart Aneurysm 26 0.037
261
HYP203 Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extrapyramidal Syndrome 26 0.037
262
CPT003 Cpt Deficiency, Hepatic, Type Ia 25 0.037
263
P SYS007 Systemic Capillary Leak Syndrome 25 0.037
264
CPL011 Capillary Malformations, Congenital, 1, Somatic, Mosaic 24 0.037
265
FDB001 Foodborne Botulism 24 0.037
266
SDD002 Sudden Infant Death with Dysgenesis of the Testes Syndrome 24 0.037
267
TRT006 Torticollis Keloids Cryptorchidism Renal Dysplasia 22 0.037
268
MTC068 Mitochondrial Complex V Deficiency, Nuclear Type 2 22 0.037
269
MCL055 Mcleod Syndrome with or Without Chronic Granulomatous Disease 22 0.037
270
BRC019 Brachycephalofrontonasal Dysplasia 22 0.037
271
LWN001 Lown-Ganong-Levine Syndrome 21 0.037
272
DMD003 Dmd-Associated Dilated Cardiomyopathy 21 0.037
273
XLN031 X-Linked Visceral Heterotaxy 1 21 0.037
274
EHL044 Ehlers-Danlos Syndrome, Autosomal Recessive, Due to Tenascin X Deficiency 21 0.037
275
c BNG076 Benign Exophthalmos Syndrome 21 0.037
276
LFT001 Left Bundle Branch Hemiblock 20 0.037
277
PGD001 Pagod Syndrome 20 0.037
278
PRN037 Prinzmetal's Variant Angina 19 0.037
279
ANT054 Anotia 19 0.037
280
CPT005 Cpt Ii Deficiency, Lethal Neonatal 19 0.037
281
DFN007 Deafness Enamel Hypoplasia Nail Defects 19 0.037
282
SPN148 Spondylometaphyseal Dysplasia Sedaghatian Type 19 0.037
283
AND005 Androgen Insensitivity Syndrome, Mild 18 0.037
284
CPT004 Cpt Deficiency, Hepatic, Type Ii 18 0.037
285
TBT001 Tabatznik Syndrome 18 0.037
286
16P006 16p11.2p12.2 Microdeletion Syndrome 18 0.037
287
DRG014 Drug-Induced Autoimmune Hemolytic Anemia 17 0.037
288
WLL009 Woolly Hair Hypotrichosis Everted Lower Lip and Outstanding Ears 17 0.037
289
INT062 Interstitial Myocarditis 16 0.037
290
PLY088 Polyvalvular Heart Disease Syndrome 16 0.037
291
ATM069 Autoimmune Hemolytic Anemia, Warm Type 15 0.037
292
P 19P001 19p13.12 Microdeletion Syndrome 15 0.037
293
NTH002 Nathalie Syndrome 15 0.037
294
c EMR004 Emery-Dreifuss Muscular Dystrophy, X-Linked 15 0.037
295
VNT011 Ventricular Fibrillation, Familial, 1 15 0.037
296
SHP003 Shapiro Syndrome 14 0.037
297
ECT023 Ectodermal Dysplasia, Hidrotic, Christianson-Fourie Type 14 0.037
298
HRS003 Hirschsprung Disease Ganglioneuroblastoma 14 0.037
299
SBR006 Subaortic Stenosis Short Stature Syndrome 14 0.037
300
TXC010 Toxic Myocarditis 14 0.037
301
MXD035 Mixed-Type Autoimmune Hemolytic Anemia 14 0.037
302
c FML196 Familial Isolated Hypoparathyroidism Due to Agenesis of Parathyroid Gland 13 0.037
303
EXT038 Extrasystoles Short Stature Hyperpigmentation Microcephaly 13 0.037
304
SBN001 Subendocardial Myocardial Infarction 13 0.037
305
MLT131 Multifocal Atrial Tachycardia 12 0.037
306
PLY042 Polyneuropathy Mental Retardation Acromicria Premature Menopause 12 0.037
307
c CRD154 Cardiomyopathy, Familial Hypertrophic 6 12 0.037
308
c VNT026 Ventricular Septal Defect 2 11 0.037
309
CRD023 Cardiomyopathy Cataract Hip Spine Disease 11 0.037
310
c VNT024 Ventricular Septal Defect 3 11 0.037
311
MSC030 Muscular Fibrosis Multifocal Obstructed Vessels 10 0.037
312
RBB001 Ribbing Disease 9 0.037
313
c EMR003 Emery-Dreifuss Muscular Dystrophy, Dominant Type 3 0.037