Search results for "arrhythmia"

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

360 hits were found for 'arrhythmia'

# Family MCID Name MIFTS Score
1
PHC009 Phocomelia Ectrodactyly Deafness Sinus Arrhythmia 19 4.678
2
WLF001 Wolff-Parkinson-White Syndrome 73 3.430
3
SDD004 Sudden Arrhythmia Death Syndrome 13 3.375
4
PHC010 Phocomelia-Ectrodactyly Ear Malformation Deafness and Sinus Arrhythmia 4 3.317
5
CRD054 Cardiac Arrhythmia, Ankyrin-B-Related 8 3.276
6
OGD001 Ogden Syndrome 21 2.316
7
P MYC007 Myocardial Infarction 93 0.199
8
c LNG028 Long Qt Syndrome 65 0.199
9
c BRG001 Brugada Syndrome 59 0.145
10
c ACT075 Acute Myocardial Infarction 60 0.141
11
P MTR005 Mitral Valve Prolapse 59 0.141
12
c CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 57 0.141
13
P DLT002 Dilated Cardiomyopathy 88 0.136
14
c SCK002 Sick Sinus Syndrome 58 0.131
15
AND003 Andersen-Tawil Syndrome 54 0.127
16
P HYP075 Hypertension 87 0.117
17
P SRC013 Sarcoidosis 75 0.117
18
c HYP061 Hypertrophic Cardiomyopathy 65 0.117
19
HYP005 Hypokalemia 50 0.117
20
SYN036 Syncope 44 0.117
21
CRD003 Cardiac Sarcoidosis 52 0.111
22
ISC004 Ischemia 63 0.105
23
c MYT002 Myotonic Dystrophy 62 0.105
24
P MYC008 Myocarditis 58 0.099
25
CNG034 Congestive Heart Failure 78 0.093
26
TTR001 Tetralogy of Fallot 75 0.093
27
TRN044 Transposition of the Great Arteries 49 0.093
28
ANR040 Aneurysm 46 0.093
29
c HYP051 Hypokalemic Periodic Paralysis 62 0.086
30
NRP001 Neuropathy 62 0.086
31
c ATN004 Autonomic Neuropathy 50 0.086
32
ATR055 Atrial Septal Aneurysm 23 0.086
33
SPS077 Sepsis 70 0.079
34
P LNG044 Long Qt Syndrome 1 68 0.079
35
P SYS005 Systemic Scleroderma 66 0.079
36
P MYT006 Myotonic Dystrophy Type 1 60 0.079
37
HYP006 Hypertensive Heart Disease 50 0.079
38
DBT002 Diabetic Autonomic Neuropathy 49 0.079
39
FBR012 Fabry Disease 86 0.070
40
c MSC005 Muscular Dystrophy 62 0.070
41
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 56 0.070
42
P JRV001 Jervell-Lange Nielsen Syndrome 49 0.070
43
HYP017 Hypophosphatemia 49 0.070
44
CRD137 Cardiogenic Shock 49 0.070
45
c LFT003 Left Ventricular Noncompaction 43 0.070
46
SYS003 Systolic Heart Failure 38 0.070
47
P RTT002 Rett Syndrome 83 0.061
48
P SDD001 Sudden Infant Death Syndrome 71 0.061
49
P CNG401 Congenital Heart Disease 69 0.061
50
P FML032 Familial Hypertrophic Cardiomyopathy 68 0.061
51
c HYP076 Hyperthyroidism 64 0.061
52
P TMT001 Timothy Syndrome 55 0.061
53
ATR057 Atrioventricular Block 52 0.061
54
c ACT076 Acute Myocarditis 47 0.061
55
c SHR030 Short Qt Syndrome 47 0.061
56
c THY054 Thyrotoxic Periodic Paralysis 46 0.061
57
CRP018 Cor Pulmonale 45 0.061
58
CRN030 Coronary Stenosis 43 0.061
59
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 42 0.061
60
P VNT013 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1 41 0.061
61
INF013 Inferior Myocardial Infarction 40 0.061
62
CRB009 Cerebritis 39 0.061
63
GNT019 Giant Cell Myocarditis 38 0.061
64
SPN148 Spondylometaphyseal Dysplasia Sedaghatian Type 26 0.061
65
P TBR001 Tuberous Sclerosis 86 0.050
66
P HMC003 Hemochromatosis 83 0.050
67
VNH001 Von Hippel-Lindau Disease 81 0.050
68
ACR007 Acromegaly 80 0.050
69
P RFS001 Refsum Disease 77 0.050
70
RLP001 Relapsing Polychondritis 72 0.050
71
P PRP001 Propionic Acidemia 71 0.050
72
P RSP003 Respiratory Failure 70 0.050
73
c SPN046 Spinal Muscular Atrophy 66 0.050
74
RHM001 Rheumatic Fever 66 0.050
75
c SCL016 Scleroderma 65 0.050
76
CST001 Costello Syndrome 65 0.050
77
BRT005 Barth Syndrome 65 0.050
78
CRN018 Coronary Artery Anomaly 63 0.050
79
CHG001 Chagas Disease 63 0.050
80
SPN186 Spinal Cord Injury 62 0.050
81
PTN001 Patent Foramen Ovale 62 0.050
82
P GLY008 Glycogen Storage Disease Ii 62 0.050
83
P PLY019 Polyneuropathy 61 0.050
84
c SLP006 Sleep Apnea 59 0.050
85
PLY041 Polymyositis 59 0.050
86
PRC012 Pericardial Effusion 58 0.050
87
SNS001 Sensorineural Hearing Loss 57 0.050
88
SCN006 Secondary Syphilis 57 0.050
89
SPR004 Supravalvular Aortic Stenosis 54 0.050
90
P LDD002 Liddle Syndrome 54 0.050
91
P MSC003 Muscular Atrophy 54 0.050
92
HYP037 Hyperhomocysteinemia 53 0.050
93
OBS006 Obstructive Lung Disease 53 0.050
94
MYC005 Myocardial Stunning 52 0.050
95
CCN002 Cocaine Abuse 51 0.050
96
c EMR001 Emery-Dreifuss Muscular Dystrophy 51 0.050
97
P ATN005 Autonomic Dysfunction 47 0.050
98
FCL014 Focal Epilepsy 47 0.050
99
c HYP052 Hyperkalemic Periodic Paralysis 46 0.050
100
PRP009 Peripartum Cardiomyopathy 43 0.050
101
DXT001 Dextrocardia 43 0.050
102
CRN041 Carnitine-Acylcarnitine Translocase Deficiency 43 0.050
103
PHC013 Phaeochromocytoma 43 0.050
104
P SPL033 Split-Hand/foot Malformation 6 41 0.050
105
STR037 Stress Cardiomyopathy 41 0.050
106
RGH001 Right Bundle Branch Block 37 0.050
107
c SPL037 Split Hand Foot Malformation 35 0.050
108
PHN011 Phenytoin Toxicity 35 0.050
109
c LNG048 Long Qt Syndrome 3 31 0.050
110
c PHC014 Phocomelia 30 0.050
111
c LNG047 Long Qt Syndrome 2 29 0.050
112
GST007 Gastric Dilatation 28 0.050
113
CPT005 Cpt Ii Deficiency, Lethal Neonatal 28 0.050
114
c LNG053 Long Qt Syndrome 9 26 0.050
115
c CRD132 Cardiac Conduction Defect 26 0.050
116
c LNG050 Long Qt Syndrome 5 23 0.050
117
SCN049 Second-Degree Atrioventricular Block 20 0.050
118
c LNG051 Long Qt Syndrome 6 19 0.050
119
HSB001 His Bundle Tachycardia 18 0.050
120
c LNG057 Long Qt Syndrome 13 18 0.050
121
c LNG049 Long Qt Syndrome 4 17 0.050
122
c LNG046 Long Qt Syndrome 11 17 0.050
123
c LNG056 Long Qt Syndrome 12 15 0.050
124
CNG288 Congenital Absence of Upper Arm and Forearm with Hand Present 14 0.050
125
P HNT001 Huntington's Disease 87 0.035
126
MRF001 Marfan Syndrome 85 0.035
127
CDS001 Cadasil 84 0.035
128
AND002 Androgen Insensitivity Syndrome 80 0.035
129
P WSK001 Wiskott-Aldrich Syndrome 79 0.035
130
P MTH008 Methylmalonic Acidemia 79 0.035
131
ACT033 Acute Intermittent Porphyria 78 0.035
132
P BPL003 Bipolar Disorder 77 0.035
133
ANK002 Ankylosing Spondylitis 77 0.035
134
P PRM021 Primary Pulmonary Hypertension 77 0.035
135
P RBN001 Rubinstein-Taybi Syndrome 76 0.035
136
KWS002 Kawasaki Disease 76 0.035
137
DCH001 Duchenne Muscular Dystrophy 75 0.035
138
P THY014 Thyroid Medullary Carcinoma 74 0.035
139
P WGN002 Wegener's Granulomatosis 74 0.035
140
ASP006 Aspergillosis 73 0.035
141
c ESS002 Essential Hypertension 73 0.035
142
c PLM037 Pulmonary Hypertension 73 0.035
143
c HYP095 Hypercholesterolemia 73 0.035
144
P TMP003 Temporal Arteritis 72 0.035
145
P DRM010 Dermatomyositis 71 0.035
146
P PRM005 Primary Hyperparathyroidism 71 0.035
147
P ANG001 Angelman Syndrome 70 0.035
148
VSC007 Vascular Disease 70 0.035
149
P MGR002 Migraine 70 0.035
150
ATH003 Atherosclerosis 69 0.035
151
PLY017 Polyarteritis Nodosa 69 0.035
152
ANX002 Anxiety Disorder 69 0.035
153
ART021 Arteriosclerosis 68 0.035
154
P AMY004 Amyloidosis 68 0.035
155
c MNN013 Meningitis 68 0.035
156
P NNN008 Noonan Syndrome 1 68 0.035
157
PRP027 Peripheral Vascular Disease 68 0.035
158
c AXN002 Axenfeld-Rieger Syndrome 67 0.035
159
P HYP056 Hypoglycemia 67 0.035
160
P CNG030 Congenital Muscular Dystrophy 67 0.035
161
P EPL025 Epileptic Encephalopathy, Early Infantile, 2 67 0.035
162
P INS005 Insulin Resistance 65 0.035
163
LYM017 Lyme Disease 65 0.035
164
c HYP069 Hyperparathyroidism 65 0.035
165
HYP004 Hypercalcemia 65 0.035
166
P CNG042 Congenital Central Hypoventilation Syndrome 65 0.035
167
ART019 Aortic Valve Stenosis 64 0.035
168
STT002 Status Asthmaticus 64 0.035
169
P CNT004 Centronuclear Myopathy 63 0.035
170
KRN002 Kearns-Sayre Syndrome 63 0.035
171
c HYP055 Hypoplastic Left Heart Syndrome 63 0.035
172
P MTR012 Mitral Valve Disease 63 0.035
173
LBR002 Leber Hereditary Optic Neuropathy 62 0.035
174
P MYP004 Myopathy 62 0.035
175
TYP007 Typhoid Fever 62 0.035
176
P ATM010 Autoimmune Hemolytic Anemia 62 0.035
177
ART111 Artery Disease 62 0.035
178
c LMB006 Limb-Girdle Muscular Dystrophy 61 0.035
179
HMR004 Hemorrhagic Fever with Renal Syndrome 61 0.035
180
BTL001 Botulism 60 0.035
181
P MLS001 Melas Syndrome 60 0.035
182
CRT002 Cartilage-Hair Hypoplasia 60 0.035
183
MTR046 Maternally Inherited Diabetes and Deafness 59 0.035
184
c LCL006 Localized Scleroderma 59 0.035
185
CND002 Conduct Disorder 59 0.035
186
MYC002 Mycobacterium Avium Complex Disease 59 0.035
187
YLL002 Yellow Fever 59 0.035
188
LPD010 Lipodystrophy 59 0.035
189
CNN005 Connective Tissue Disease 58 0.035
190
END030 End Stage Renal Failure 58 0.035
191
P SYP003 Syphilis 58 0.035
192
P CRV039 Cervicitis 58 0.035
193
ISC006 Ischemic Heart Disease 58 0.035
194
THY033 Thyrotoxicosis 58 0.035
195
HYP266 Hypoxia 58 0.035
196
RLY001 Riley-Day Syndrome 58 0.035
197
TNS005 Tonsillitis 57 0.035
198
PTN002 Patent Ductus Arteriosus 57 0.035
199
P END033 Endocarditis 57 0.035
200
DDN006 Duodenitis 56 0.035
201
EPD037 Epidermal Nevus 56 0.035
202
MCR103 Microtia 56 0.035
203
P OCL013 Oculodentodigital Dysplasia 56 0.035
204
MCR088 Microscopic Polyangiitis 56 0.035
205
c MYT007 Myotonic Dystrophy Type 2 56 0.035
206
P HLP012 Holoprosencephaly-3 55 0.035
207
CRD001 Cardiac Tamponade 55 0.035
208
MTN003 Motion Sickness 55 0.035
209
IMP005 Impotence 55 0.035
210
c PSD015 Pseudohypoparathyroidism 55 0.035
211
P STC005 Stickler Syndrome Type 1 55 0.035
212
EBS001 Ebstein Anomaly 55 0.035
213
LGN002 Legionellosis 55 0.035
214
ANH002 Anhidrosis 54 0.035
215
c LPR012 Leopard Syndrome 1 54 0.035
216
c BRT004 Bartter Disease 54 0.035
217
c SMP003 Simpson-Golabi-Behmel Syndrome 54 0.035
218
P HYP192 Hypocalcemia, Autosomal Dominant 53 0.035
219
c GLY007 Glycogen Storage Disease Iv 53 0.035
220
INV001 Invasive Aspergillosis 53 0.035
221
c CNT048 Central Hypoventilation Syndrome 53 0.035
222
c RST002 Restrictive Cardiomyopathy 53 0.035
223
c CNG012 Congenital Generalized Lipodystrophy 53 0.035
224
TRN015 Transient Cerebral Ischemia 53 0.035
225
AGG002 Aggressive Systemic Mastocytosis 52 0.035
226
THR013 Thoracic Outlet Syndrome 52 0.035
227
AGR002 Agoraphobia 51 0.035
228
END072 Endotheliitis 51 0.035
229
GRN037 Granulomatosis with Polyangiitis 51 0.035
230
P MJR001 Major Depressive Disorder 50 0.035
231
CRN055 Carney Triad 50 0.035
232
P NRV007 Nervous System Disease 50 0.035
233
P CNT015 Central Sleep Apnea 50 0.035
234
ATX019 Ataxia with Vitamin E Deficiency 50 0.035
235
BRN106 Burns 50 0.035
236
TRY001 Trypanosomiasis 50 0.035
237
FBR047 Fibromyalgia 50 0.035
238
DRG003 Drug Dependence 49 0.035
239
ALC010 Alcoholic Cardiomyopathy 49 0.035
240
c PSD003 Pseudohypoaldosteronism 49 0.035
241
c CNT035 Central Nervous System Disease 49 0.035
242
P DYS021 Dysautonomia 49 0.035
243
EHL034 Ehlers-Danlos Syndrome, Hypermobility Type 49 0.035
244
c CNG018 Congenital Heart Block 48 0.035
245
P MLG090 Malignant Hyperthermia Susceptibility Type 1 48 0.035
246
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 48 0.035
247
HTR003 Heterotaxy 48 0.035
248
CRT008 Carotid Artery Dissection 48 0.035
249
NXS001 Naxos Disease 47 0.035
250
FTT003 Fatty Acid Oxidation Disorders 47 0.035
251
END021 Endomyocardial Fibrosis 47 0.035
252
PNN001 Panniculitis 47 0.035
253
ART004 Aortic Atherosclerosis 46 0.035
254
INF034 Infective Endocarditis 45 0.035
255
P FCS001 Facioscapulohumeral Muscular Dystrophy 45 0.035
256
P MYH004 Myh9 Related Thrombocytopenia 45 0.035
257
CTS011 Cutis Marmorata Telangiectatica Congenita 45 0.035
258
P DMN023 Diamond-Blackfan Anemia 1 45 0.035
259
ESN011 Eisenmenger Syndrome 45 0.035
260
LYM029 Lymphedema-Distichiasis Syndrome 44 0.035
261
TRN012 Transient Global Amnesia 44 0.035
262
NRN002 Neuronitis 44 0.035
263
P HYP216 Hypoparathyroidism Familial Isolated 43 0.035
264
HYP022 Hypohidrosis 43 0.035
265
P MYF003 Myofibrillar Myopathy 43 0.035
266
P PRX064 Peroxisome Biogenesis Disorder 2b 41 0.035
267
PLM068 Pulmonary Vein Stenosis 41 0.035
268
c FML058 Familial Dilated Cardiomyopathy 40 0.035
269
TRC062 Tricuspid Atresia 40 0.035
270
P HRT021 Heart Block, Progressive, Type Ia 39 0.035
271
P KLF001 Kleefstra Syndrome 39 0.035
272
c CNG045 Congenital Dyserythropoietic Anemia Type I 39 0.035
273
ESN020 Eosinophilic Granulomatosis with Polyangiitis 38 0.035
274
P SCH035 Schwartz Jampel Syndrome Type 1 38 0.035
275
ADN002 Adenoiditis 38 0.035
276
MNN032 Meningococcal Meningitis 38 0.035
277
BRN055 Bronchogenic Cyst 38 0.035
278
P SYS007 Systemic Capillary Leak Syndrome 37 0.035
279
c FML162 Familial Mediterranean Fever, Ad 37 0.035
280
PCW002 Pcwh Syndrome 35 0.035
281
c CTS030 Cutis Laxa, Autosomal Recessive, Type Ia 34 0.035
282
SYN053 Syndromic Diarrhea 34 0.035
283
DPH006 Diaphragmatic Eventration 34 0.035
284
P PRX010 Paroxysmal Ventricular Fibrillation 33 0.035
285
RGH009 Right Atrial Isomerism 33 0.035
286
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 33 0.035
287
P CNG225 Congenital Dyserythropoietic Anemia Type 2 33 0.035
288
MTC028 Mitochondrial Cardiomyopathy 33 0.035
289
P HYP239 Hyperkalemic Periodic Paralysis Type 2 33 0.035
290
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 32 0.035
291
GLS004 Glossopharyngeal Neuralgia 32 0.035
292
AMT004 Amitriptyline Toxicity 31 0.035
293
CHL028 Childhood Type Dermatomyositis 31 0.035
294
ADT003 Auditory System Disease 30 0.035
295
MGL023 Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome, Somatic 30 0.035
296
CNG134 Congenitally Corrected Transposition of the Great Arteries 30 0.035
297
c HMC021 Hemochromatosis, Type 2a 30 0.035
298
P SCK014 Sick Sinus Syndrome 2 30 0.035
299
PRN037 Prinzmetal's Variant Angina 30 0.035
300
APL022 Aplasia Cutis Congenita, Reticulolinear, with Mmicrocephaly, Facial Dysmorphism and Other Congenital Anomalies 30 0.035
301
HRD040 Hereditary Angiopathy with Nephropathy, Aneurysms, and Muscle Cramps Syndrome 28 0.035
302
c MYC058 Myocardial Infarction 2 28 0.035
303
CPT003 Cpt Deficiency, Hepatic, Type Ia 28 0.035
304
HYP203 Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extrapyramidal Syndrome 28 0.035
305
ANT054 Anotia 27 0.035
306
XLN031 X-Linked Visceral Heterotaxy 1 26 0.035
307
CPL011 Capillary Malformations, Congenital, 1, Somatic, Mosaic 26 0.035
308
FDB001 Foodborne Botulism 26 0.035
309
PGD001 Pagod Syndrome 24 0.035
310
ART007 Aorta Atresia 23 0.035
311
c BNG076 Benign Exophthalmos Syndrome 22 0.035
312
BRC019 Brachycephalofrontonasal Dysplasia 22 0.035
313
MTC068 Mitochondrial Complex V Deficiency, Nuclear Type 2 22 0.035
314
EHL044 Ehlers-Danlos Syndrome, Autosomal Recessive, Due to Tenascin X Deficiency 22 0.035
315
LWN001 Lown-Ganong-Levine Syndrome 22 0.035
316
SDD002 Sudden Infant Death with Dysgenesis of the Testes Syndrome 22 0.035
317
c BSL014 Basilar Migraine 21 0.035
318
MCL055 Mcleod Syndrome with or Without Chronic Granulomatous Disease 21 0.035
319
DRG014 Drug-Induced Autoimmune Hemolytic Anemia 21 0.035
320
AND005 Androgen Insensitivity Syndrome, Mild 21 0.035
321
TRT006 Torticollis Keloids Cryptorchidism Renal Dysplasia 21 0.035
322
P HRT017 Heart Tumor 21 0.035
323
TBT001 Tabatznik Syndrome 20 0.035
324
SHP003 Shapiro Syndrome 20 0.035
325
MXD035 Mixed-Type Autoimmune Hemolytic Anemia 20 0.035
326
DFN007 Deafness Enamel Hypoplasia Nail Defects 20 0.035
327
DMD003 Dmd-Associated Dilated Cardiomyopathy 19 0.035
328
NTH002 Nathalie Syndrome 18 0.035
329
CPT004 Cpt Deficiency, Hepatic, Type Ii 18 0.035
330
16P006 16p11.2p12.2 Microdeletion Syndrome 18 0.035
331
ATM069 Autoimmune Hemolytic Anemia, Warm Type 18 0.035
332
WLL009 Woolly Hair Hypotrichosis Everted Lower Lip and Outstanding Ears 18 0.035
333
CRD023 Cardiomyopathy Cataract Hip Spine Disease 17 0.035
334
DXR001 Doxorubicin Induced Cardiomyopathy 17 0.035
335
MLT131 Multifocal Atrial Tachycardia 17 0.035
336
VNT011 Ventricular Fibrillation, Familial, 1 17 0.035
337
c BRG009 Brugada Syndrome 7 17 0.035
338
P 19P001 19p13.12 Microdeletion Syndrome 16 0.035
339
SBR006 Subaortic Stenosis Short Stature Syndrome 16 0.035
340
INT062 Interstitial Myocarditis 15 0.035
341
MCR033 Macrocephaly-Capillary Malformation 15 0.035
342
TXC010 Toxic Myocarditis 15 0.035
343
ECT023 Ectodermal Dysplasia, Hidrotic, Christianson-Fourie Type 15 0.035
344
HRS003 Hirschsprung Disease Ganglioneuroblastoma 15 0.035
345
EXT038 Extrasystoles Short Stature Hyperpigmentation Microcephaly 15 0.035
346
c FML196 Familial Isolated Hypoparathyroidism Due to Agenesis of Parathyroid Gland 15 0.035
347
RBB001 Ribbing Disease 14 0.035
348
c VNT028 Ventricular Septal Defect 1 14 0.035
349
c CRD154 Cardiomyopathy, Familial Hypertrophic 6 13 0.035
350
PLY088 Polyvalvular Heart Disease Syndrome 13 0.035
351
c VNT024 Ventricular Septal Defect 3 13 0.035
352
c VNT026 Ventricular Septal Defect 2 13 0.035
353
SBN001 Subendocardial Myocardial Infarction 13 0.035
354
DGT004 Digitalis Poisoning 12 0.035
355
c EMR004 Emery-Dreifuss Muscular Dystrophy, X-Linked 11 0.035
356
PLY106 Polyneuropathy - Intellectual Disability - Acromicria - Premature Menopause 11 0.035
357
MSC030 Muscular Fibrosis Multifocal Obstructed Vessels 11 0.035
358
ARR041 Arrhythmogenic Right Ventricular Dysplasia, Familial, 13 8 0.035
359
CRN208 Coronary Sinus Atresia 8 0.035
360
c EMR003 Emery-Dreifuss Muscular Dystrophy, Dominant Type 7 0.035