Search results for "arrhythmia"

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

349 hits were found for 'arrhythmia'

# Family MCID Name MIFTS Score
1
PHC009 Phocomelia Ectrodactyly Deafness Sinus Arrhythmia 19 4.458
2
SDD004 Sudden Arrhythmia Death Syndrome 13 3.221
3
PHC010 Phocomelia-Ectrodactyly Ear Malformation Deafness and Sinus Arrhythmia 4 3.162
4
CRD054 Cardiac Arrhythmia, Ankyrin-B-Related 7 3.120
5
WLF001 Wolff-Parkinson-White Syndrome 70 2.361
6
SDD005 Sudden Cardiac Death Multi-Gene Panels 13 2.258
7
OGD001 Ogden Syndrome 19 2.206
8
c CRD152 Cardiomyopathy, Familial Hypertrophic, 21 15 2.206
9
P MYC007 Myocardial Infarction 92 0.205
10
c LNG028 Long Qt Syndrome 64 0.196
11
c ACT075 Acute Myocardial Infarction 59 0.147
12
P DLT002 Dilated Cardiomyopathy 82 0.138
13
c CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 55 0.138
14
c BRG001 Brugada Syndrome 55 0.134
15
P MTR005 Mitral Valve Prolapse 59 0.129
16
c SCK002 Sick Sinus Syndrome 56 0.129
17
ARR001 Arrhythmogenic Right Ventricular Dysplasia 50 0.124
18
P HYP075 Hypertension 85 0.119
19
c SRC013 Sarcoidosis 68 0.113
20
c HYP061 Hypertrophic Cardiomyopathy 63 0.113
21
AND003 Andersen-Tawil Syndrome 53 0.113
22
HYP005 Hypokalemia 47 0.113
23
SYN036 Syncope 44 0.113
24
c MYT002 Myotonic Dystrophy 65 0.107
25
ISC004 Ischemia 63 0.107
26
CRD003 Cardiac Sarcoidosis 51 0.107
27
P MYC008 Myocarditis 57 0.101
28
CNG034 Congestive Heart Failure 78 0.095
29
TTR001 Tetralogy of Fallot 74 0.095
30
TRN044 Transposition of the Great Arteries 49 0.095
31
ANR040 Aneurysm 44 0.095
32
ATR055 Atrial Septal Aneurysm 23 0.088
33
NRP001 Neuropathy 61 0.080
34
c HYP051 Hypokalemic Periodic Paralysis 61 0.080
35
P MYT006 Myotonic Dystrophy Type 1 57 0.080
36
HYP006 Hypertensive Heart Disease 50 0.080
37
c ATN004 Autonomic Neuropathy 49 0.080
38
P LNG044 Long Qt Syndrome 1 66 0.071
39
c MSC005 Muscular Dystrophy 62 0.071
40
DBT002 Diabetic Autonomic Neuropathy 49 0.071
41
CRD137 Cardiogenic Shock 48 0.071
42
SYS003 Systolic Heart Failure 37 0.071
43
CRN211 Coronary Artery Disease 84 0.062
44
P SDD001 Sudden Infant Death Syndrome 71 0.062
45
P SYS005 Systemic Scleroderma 66 0.062
46
c HYP076 Hyperthyroidism 62 0.062
47
P CNG401 Congenital Heart Disease 58 0.062
48
P TMT001 Timothy Syndrome 52 0.062
49
P JRV001 Jervell-Lange Nielsen Syndrome 49 0.062
50
c ACT076 Acute Myocarditis 46 0.062
51
c THY054 Thyrotoxic Periodic Paralysis 46 0.062
52
CRP018 Cor Pulmonale 44 0.062
53
CRN030 Coronary Stenosis 43 0.062
54
c LFT003 Left Ventricular Noncompaction 43 0.062
55
INF013 Inferior Myocardial Infarction 40 0.062
56
GNT019 Giant Cell Myocarditis 38 0.062
57
SPN148 Spondylometaphyseal Dysplasia Sedaghatian Type 25 0.062
58
P RTT002 Rett Syndrome 82 0.051
59
ACR007 Acromegaly 79 0.051
60
P RFS001 Refsum Disease 72 0.051
61
SPS077 Sepsis 70 0.051
62
P RSP003 Respiratory Failure 68 0.051
63
c SPN046 Spinal Muscular Atrophy 65 0.051
64
P FML032 Familial Hypertrophic Cardiomyopathy 65 0.051
65
c SCL016 Scleroderma 64 0.051
66
BRT005 Barth Syndrome 64 0.051
67
SPN186 Spinal Cord Injury 63 0.051
68
PTN001 Patent Foramen Ovale 61 0.051
69
P PLY019 Polyneuropathy 60 0.051
70
c SLP006 Sleep Apnea 59 0.051
71
PLY041 Polymyositis 58 0.051
72
PRC012 Pericardial Effusion 58 0.051
73
SCN006 Secondary Syphilis 57 0.051
74
SNS001 Sensorineural Hearing Loss 57 0.051
75
P MSC003 Muscular Atrophy 53 0.051
76
ATR057 Atrioventricular Block 51 0.051
77
MYC005 Myocardial Stunning 51 0.051
78
HYP037 Hyperhomocysteinemia 51 0.051
79
OBS006 Obstructive Lung Disease 51 0.051
80
CCN002 Cocaine Abuse 50 0.051
81
c EMR001 Emery-Dreifuss Muscular Dystrophy 49 0.051
82
P ATN005 Autonomic Dysfunction 46 0.051
83
c SHR030 Short Qt Syndrome 46 0.051
84
FCL014 Focal Epilepsy 45 0.051
85
c HYP052 Hyperkalemic Periodic Paralysis 44 0.051
86
DXT001 Dextrocardia 43 0.051
87
PRP009 Peripartum Cardiomyopathy 43 0.051
88
PHC013 Phaeochromocytoma 42 0.051
89
STR037 Stress Cardiomyopathy 41 0.051
90
P SPL033 Split-Hand/foot Malformation 6 41 0.051
91
CRB009 Cerebritis 39 0.051
92
RGH001 Right Bundle Branch Block 36 0.051
93
c SPL037 Split Hand Foot Malformation 35 0.051
94
c LNG048 Long Qt Syndrome 3 31 0.051
95
c PHC014 Phocomelia 28 0.051
96
c LNG047 Long Qt Syndrome 2 28 0.051
97
GST007 Gastric Dilatation 28 0.051
98
c CRD132 Cardiac Conduction Defect 28 0.051
99
c LNG053 Long Qt Syndrome 9 28 0.051
100
c LNG050 Long Qt Syndrome 5 23 0.051
101
c LNG051 Long Qt Syndrome 6 20 0.051
102
HSB001 His Bundle Tachycardia 19 0.051
103
c LNG057 Long Qt Syndrome 13 19 0.051
104
c LNG049 Long Qt Syndrome 4 18 0.051
105
c VNT013 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1 17 0.051
106
c LNG046 Long Qt Syndrome 11 17 0.051
107
c LNG056 Long Qt Syndrome 12 16 0.051
108
CNG288 Congenital Absence of Upper Arm and Forearm with Hand Present 15 0.051
109
P HNT001 Huntington's Disease 85 0.036
110
P TBR001 Tuberous Sclerosis 85 0.036
111
CDS001 Cadasil 84 0.036
112
MRF001 Marfan Syndrome 83 0.036
113
P PRM021 Primary Pulmonary Hypertension 82 0.036
114
FBR012 Fabry Disease 81 0.036
115
AND002 Androgen Insensitivity Syndrome 80 0.036
116
VNH001 Von Hippel-Lindau Disease 80 0.036
117
P HMC003 Hemochromatosis 78 0.036
118
P WSK001 Wiskott-Aldrich Syndrome 78 0.036
119
P MTH008 Methylmalonic Acidemia 77 0.036
120
ACT033 Acute Intermittent Porphyria 76 0.036
121
P BPL003 Bipolar Disorder 75 0.036
122
ANK002 Ankylosing Spondylitis 74 0.036
123
DCH001 Duchenne Muscular Dystrophy 74 0.036
124
KWS002 Kawasaki Disease 73 0.036
125
P THY014 Thyroid Medullary Carcinoma 73 0.036
126
c ESS002 Essential Hypertension 72 0.036
127
ASP006 Aspergillosis 72 0.036
128
P TMP003 Temporal Arteritis 71 0.036
129
P WGN002 Wegener's Granulomatosis 71 0.036
130
P ANG001 Angelman Syndrome 70 0.036
131
RLP001 Relapsing Polychondritis 70 0.036
132
c HYP095 Hypercholesterolemia 70 0.036
133
P PRP001 Propionic Acidemia 70 0.036
134
VSC007 Vascular Disease 70 0.036
135
PLY017 Polyarteritis Nodosa 69 0.036
136
c CNG006 Congenital Hypothyroidism 69 0.036
137
P MGR002 Migraine 69 0.036
138
ATH003 Atherosclerosis 68 0.036
139
P PRM005 Primary Hyperparathyroidism 68 0.036
140
ANX002 Anxiety Disorder 68 0.036
141
P DRM010 Dermatomyositis 68 0.036
142
c MNN013 Meningitis 68 0.036
143
PRP027 Peripheral Vascular Disease 67 0.036
144
P AMY004 Amyloidosis 67 0.036
145
ART021 Arteriosclerosis 67 0.036
146
P NNN008 Noonan Syndrome 1 66 0.036
147
P SYS004 Systemic Mastocytosis 66 0.036
148
P INS005 Insulin Resistance 66 0.036
149
c AXN002 Axenfeld-Rieger Syndrome 66 0.036
150
P CNG030 Congenital Muscular Dystrophy 65 0.036
151
HYP004 Hypercalcemia 65 0.036
152
LYM017 Lyme Disease 64 0.036
153
CST001 Costello Syndrome 64 0.036
154
c HYP069 Hyperparathyroidism 64 0.036
155
ART019 Aortic Valve Stenosis 64 0.036
156
P CNG042 Congenital Central Hypoventilation Syndrome 64 0.036
157
HYP056 Hypoglycemia 63 0.036
158
CHG001 Chagas Disease 62 0.036
159
RHM001 Rheumatic Fever 62 0.036
160
P HYP055 Hypoplastic Left Heart Syndrome 62 0.036
161
P MTR012 Mitral Valve Disease 62 0.036
162
c MYP004 Myopathy 62 0.036
163
CTN014 Cutaneous Mastocytosis 61 0.036
164
P GLY008 Glycogen Storage Disease Ii 61 0.036
165
STT002 Status Asthmaticus 60 0.036
166
TYP007 Typhoid Fever 60 0.036
167
HMR004 Hemorrhagic Fever with Renal Syndrome 60 0.036
168
ART111 Artery Disease 60 0.036
169
BTL001 Botulism 60 0.036
170
SNG010 Single Median Maxillary Central Incisor 60 0.036
171
c LMB006 Limb-Girdle Muscular Dystrophy 60 0.036
172
P MLS001 Melas Syndrome 59 0.036
173
LPD010 Lipodystrophy 59 0.036
174
CRN017 Coronary Thrombosis 59 0.036
175
CND002 Conduct Disorder 59 0.036
176
c LCL006 Localized Scleroderma 59 0.036
177
YLL002 Yellow Fever 58 0.036
178
MYC002 Mycobacterium Avium Complex Disease 58 0.036
179
CNN005 Connective Tissue Disease 58 0.036
180
END030 End Stage Renal Failure 58 0.036
181
P SYP003 Syphilis 57 0.036
182
P CRV039 Cervicitis 57 0.036
183
THY033 Thyrotoxicosis 57 0.036
184
HYP266 Hypoxia 57 0.036
185
PTN002 Patent Ductus Arteriosus 57 0.036
186
RLY001 Riley-Day Syndrome 57 0.036
187
TNS005 Tonsillitis 57 0.036
188
P END033 Endocarditis 56 0.036
189
DDN006 Duodenitis 56 0.036
190
MCR103 Microtia 55 0.036
191
P OCL013 Oculodentodigital Dysplasia 55 0.036
192
MCR088 Microscopic Polyangiitis 55 0.036
193
CRD001 Cardiac Tamponade 55 0.036
194
IMP005 Impotence 55 0.036
195
MTN003 Motion Sickness 54 0.036
196
EBS001 Ebstein Anomaly 54 0.036
197
c LPR012 Leopard Syndrome 1 54 0.036
198
c PSD015 Pseudohypoparathyroidism 54 0.036
199
c MYT007 Myotonic Dystrophy Type 2 54 0.036
200
EPD037 Epidermal Nevus 54 0.036
201
ANH002 Anhidrosis 54 0.036
202
SPR004 Supravalvular Aortic Stenosis 53 0.036
203
P HYP192 Hypocalcemia, Autosomal Dominant 53 0.036
204
c SMP003 Simpson-Golabi-Behmel Syndrome 53 0.036
205
AGG002 Aggressive Systemic Mastocytosis 52 0.036
206
INV001 Invasive Aspergillosis 52 0.036
207
c RST002 Restrictive Cardiomyopathy 52 0.036
208
P LDD002 Liddle Syndrome 52 0.036
209
c CNT048 Central Hypoventilation Syndrome 52 0.036
210
c CNG012 Congenital Generalized Lipodystrophy 52 0.036
211
c GLY007 Glycogen Storage Disease Iv 52 0.036
212
THR013 Thoracic Outlet Syndrome 52 0.036
213
TRN015 Transient Cerebral Ischemia 52 0.036
214
HTR003 Heterotaxy 51 0.036
215
c BRT004 Bartter Disease 51 0.036
216
END072 Endotheliitis 50 0.036
217
P MJR001 Major Depressive Disorder 50 0.036
218
CRN055 Carney Triad 50 0.036
219
P NRV007 Nervous System Disease 50 0.036
220
MTR046 Maternally Inherited Diabetes and Deafness 50 0.036
221
P CNT015 Central Sleep Apnea 49 0.036
222
TRY001 Trypanosomiasis 49 0.036
223
LGN002 Legionellosis 49 0.036
224
BRN106 Burns 49 0.036
225
AGR002 Agoraphobia 49 0.036
226
EHL034 Ehlers-Danlos Syndrome, Hypermobility Type 49 0.036
227
FBR047 Fibromyalgia 49 0.036
228
ATX019 Ataxia with Vitamin E Deficiency 49 0.036
229
c CNG018 Congenital Heart Block 49 0.036
230
c CNT035 Central Nervous System Disease 49 0.036
231
ALC010 Alcoholic Cardiomyopathy 48 0.036
232
HYP017 Hypophosphatemia 48 0.036
233
NXS001 Naxos Disease 47 0.036
234
FTT003 Fatty Acid Oxidation Disorders 47 0.036
235
PNN001 Panniculitis 46 0.036
236
END021 Endomyocardial Fibrosis 46 0.036
237
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 46 0.036
238
P MLG090 Malignant Hyperthermia Susceptibility Type 1 46 0.036
239
ART004 Aortic Atherosclerosis 45 0.036
240
INF034 Infective Endocarditis 45 0.036
241
P STC005 Stickler Syndrome Type 1 44 0.036
242
CTS011 Cutis Marmorata Telangiectatica Congenita 44 0.036
243
P DMN023 Diamond-Blackfan Anemia 1 44 0.036
244
P FCS001 Facioscapulohumeral Muscular Dystrophy 44 0.036
245
P PRX064 Peroxisome Biogenesis Disorder 2b 44 0.036
246
LYM029 Lymphedema-Distichiasis Syndrome 44 0.036
247
TRN012 Transient Global Amnesia 43 0.036
248
NRN002 Neuronitis 43 0.036
249
HYP022 Hypohidrosis 43 0.036
250
CRN041 Carnitine-Acylcarnitine Translocase Deficiency 43 0.036
251
P HYP216 Hypoparathyroidism Familial Isolated 41 0.036
252
TRC062 Tricuspid Atresia 41 0.036
253
P MYH004 Myh9 Related Thrombocytopenia 41 0.036
254
P HRT021 Heart Block, Progressive, Type Ia 41 0.036
255
PLM068 Pulmonary Vein Stenosis 41 0.036
256
P EPL025 Epileptic Encephalopathy, Early Infantile, 2 41 0.036
257
P MYF003 Myofibrillar Myopathy 40 0.036
258
c CNG045 Congenital Dyserythropoietic Anemia Type I 39 0.036
259
BRN055 Bronchogenic Cyst 38 0.036
260
P SCH035 Schwartz Jampel Syndrome Type 1 38 0.036
261
MNN032 Meningococcal Meningitis 38 0.036
262
ADN002 Adenoiditis 38 0.036
263
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 37 0.036
264
P SYS007 Systemic Capillary Leak Syndrome 37 0.036
265
P KLF001 Kleefstra Syndrome 37 0.036
266
c FML058 Familial Dilated Cardiomyopathy 37 0.036
267
P VNT010 Ventricular Tachycardia, Catecholaminergic Polymorphic, 2 37 0.036
268
c FML162 Familial Mediterranean Fever, Ad 35 0.036
269
c CTS030 Cutis Laxa, Autosomal Recessive, Type Ia 33 0.036
270
DPH006 Diaphragmatic Eventration 33 0.036
271
P PRX010 Paroxysmal Ventricular Fibrillation 33 0.036
272
MTC028 Mitochondrial Cardiomyopathy 33 0.036
273
P CNG225 Congenital Dyserythropoietic Anemia Type 2 32 0.036
274
P HYP239 Hyperkalemic Periodic Paralysis Type 2 32 0.036
275
SYN053 Syndromic Diarrhea 32 0.036
276
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 32 0.036
277
MYP007 Myopathy Due to Cpt Ii Deficiency 32 0.036
278
GLS004 Glossopharyngeal Neuralgia 31 0.036
279
CHL028 Childhood Type Dermatomyositis 31 0.036
280
P SCK014 Sick Sinus Syndrome 2 30 0.036
281
MGL023 Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome, Somatic 30 0.036
282
CNG134 Congenitally Corrected Transposition of the Great Arteries 30 0.036
283
PRN037 Prinzmetal's Variant Angina 30 0.036
284
APL022 Aplasia Cutis Congenita, Reticulolinear, with Mmicrocephaly, Facial Dysmorphism and Other Congenital Anomalies 29 0.036
285
c HMC021 Hemochromatosis, Type 2a 29 0.036
286
P VNT028 Ventricular Septal Defect 1 29 0.036
287
ADT003 Auditory System Disease 28 0.036
288
RGH009 Right Atrial Isomerism 28 0.036
289
HYP203 Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extrapyramidal Syndrome 28 0.036
290
c MYC058 Myocardial Infarction 2 28 0.036
291
ANT054 Anotia 27 0.036
292
XLN031 X-Linked Visceral Heterotaxy 1 26 0.036
293
CPL011 Capillary Malformations, Congenital, 1, Somatic, Mosaic 26 0.036
294
FDB001 Foodborne Botulism 26 0.036
295
PCW002 Pcwh Syndrome 24 0.036
296
CPT003 Cpt Deficiency, Hepatic, Type Ia 24 0.036
297
PGD001 Pagod Syndrome 23 0.036
298
ART007 Aorta Atresia 22 0.036
299
c BNG076 Benign Exophthalmos Syndrome 22 0.036
300
BRC019 Brachycephalofrontonasal Dysplasia 22 0.036
301
EHL044 Ehlers-Danlos Syndrome, Autosomal Recessive, Due to Tenascin X Deficiency 22 0.036
302
MTC068 Mitochondrial Complex V Deficiency, Nuclear Type 2 22 0.036
303
SDD002 Sudden Infant Death with Dysgenesis of the Testes Syndrome 21 0.036
304
c BSL014 Basilar Migraine 21 0.036
305
SHP003 Shapiro Syndrome 21 0.036
306
TRT006 Torticollis Keloids Cryptorchidism Renal Dysplasia 21 0.036
307
AND005 Androgen Insensitivity Syndrome, Mild 21 0.036
308
DFN007 Deafness Enamel Hypoplasia Nail Defects 20 0.036
309
HRD040 Hereditary Angiopathy with Nephropathy, Aneurysms, and Muscle Cramps Syndrome 20 0.036
310
MCL055 Mcleod Syndrome with or Without Chronic Granulomatous Disease 20 0.036
311
MXD035 Mixed-Type Autoimmune Hemolytic Anemia 20 0.036
312
DRG014 Drug-Induced Autoimmune Hemolytic Anemia 19 0.036
313
ATM069 Autoimmune Hemolytic Anemia, Warm Type 18 0.036
314
CPT005 Cpt Ii Deficiency, Lethal Neonatal 18 0.036
315
NTH002 Nathalie Syndrome 18 0.036
316
TBT001 Tabatznik Syndrome 18 0.036
317
16P006 16p11.2p12.2 Microdeletion Syndrome 18 0.036
318
DXR001 Doxorubicin Induced Cardiomyopathy 18 0.036
319
LWN001 Lown-Ganong-Levine Syndrome 18 0.036
320
CPT004 Cpt Deficiency, Hepatic, Type Ii 17 0.036
321
WLL009 Woolly Hair Hypotrichosis Everted Lower Lip and Outstanding Ears 17 0.036
322
CRD023 Cardiomyopathy Cataract Hip Spine Disease 17 0.036
323
c LNG052 Long Qt Syndrome 8 17 0.036
324
P 19P001 19p13.12 Microdeletion Syndrome 17 0.036
325
VNT011 Ventricular Fibrillation, Familial, 1 16 0.036
326
c BRG009 Brugada Syndrome 7 16 0.036
327
INT062 Interstitial Myocarditis 15 0.036
328
SCN049 Second-Degree Atrioventricular Block 15 0.036
329
SBR006 Subaortic Stenosis Short Stature Syndrome 15 0.036
330
c VNT026 Ventricular Septal Defect 2 15 0.036
331
ECT023 Ectodermal Dysplasia, Hidrotic, Christianson-Fourie Type 15 0.036
332
HRS003 Hirschsprung Disease Ganglioneuroblastoma 15 0.036
333
TXC010 Toxic Myocarditis 15 0.036
334
EXT038 Extrasystoles Short Stature Hyperpigmentation Microcephaly 14 0.036
335
c FML196 Familial Isolated Hypoparathyroidism Due to Agenesis of Parathyroid Gland 14 0.036
336
MCR033 Macrocephaly-Capillary Malformation 14 0.036
337
RBB001 Ribbing Disease 14 0.036
338
c VNT024 Ventricular Septal Defect 3 14 0.036
339
c CRD154 Cardiomyopathy, Familial Hypertrophic 6 13 0.036
340
DGT004 Digitalis Poisoning 13 0.036
341
PLY088 Polyvalvular Heart Disease Syndrome 13 0.036
342
MLT131 Multifocal Atrial Tachycardia 13 0.036
343
c EMR004 Emery-Dreifuss Muscular Dystrophy, X-Linked 12 0.036
344
SBN001 Subendocardial Myocardial Infarction 12 0.036
345
PLY106 Polyneuropathy - Intellectual Disability - Acromicria - Premature Menopause 11 0.036
346
MSC030 Muscular Fibrosis Multifocal Obstructed Vessels 11 0.036
347
CRN208 Coronary Sinus Atresia 8 0.036
348
ARR041 Arrhythmogenic Right Ventricular Dysplasia, Familial, 13 7 0.036
349
c EMR003 Emery-Dreifuss Muscular Dystrophy, Dominant Type 7 0.036