Search results for "arrhythmia"

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

394 hits were found for 'arrhythmia'

# Family MCID Name MIFTS Score
1
PHC010 Phocomelia-Ectrodactyly Ear Malformation Deafness and Sinus Arrhythmia 16 4.088
2
CRD054 Cardiac Arrhythmia, Ankyrin-B-Related 20 4.043
3
WLF001 Wolff-Parkinson-White Syndrome 65 2.463
4
SDD004 Sudden Arrhythmia Death Syndrome 9 2.409
5
PHC009 Phocomelia Ectrodactyly Deafness Sinus Arrhythmia 4 2.396
6
PRM199 Premature Aging Appearance-Developmental Delay-Cardiac Arrhythmia Syndrome 5 2.348
7
P LNG028 Long Qt Syndrome 62 0.203
8
P MYC007 Myocardial Infarction 81 0.192
9
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 58 0.145
10
P DLT002 Dilated Cardiomyopathy 77 0.138
11
P ATR011 Atrial Fibrillation 62 0.138
12
c ACT075 Acute Myocardial Infarction 57 0.138
13
P BRG001 Brugada Syndrome 56 0.138
14
P SCK002 Sick Sinus Syndrome 50 0.125
15
SYN036 Syncope 37 0.125
16
CRD003 Cardiac Sarcoidosis 44 0.116
17
P HYP061 Hypertrophic Cardiomyopathy 59 0.111
18
HYP005 Hypokalemia 42 0.111
19
P MYC008 Myocarditis 50 0.106
20
P MYT002 Myotonic Dystrophy 57 0.100
21
ISC004 Ischemia 53 0.100
22
CNG034 Congestive Heart Failure 69 0.094
23
TTR001 Tetralogy of Fallot 67 0.094
24
ANR040 Aneurysm 35 0.094
25
P AND016 Andersen Syndrome 54 0.088
26
TRN044 Transposition of the Great Arteries 41 0.088
27
P NRP001 Neuropathy 52 0.082
28
ATN004 Autonomic Neuropathy 41 0.082
29
ATR055 Atrial Septal Aneurysm 20 0.082
30
P MSC005 Muscular Dystrophy 54 0.075
31
HYP006 Hypertensive Heart Disease 43 0.075
32
DBT002 Diabetic Autonomic Neuropathy 41 0.075
33
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 38 0.075
34
P SCL016 Scleroderma 76 0.067
35
FBR012 Fabry Disease 76 0.067
36
P RTT002 Rett Syndrome 73 0.067
37
P RFS001 Refsum Disease 63 0.067
38
P CNG401 Congenital Heart Disease 62 0.067
39
c LNG044 Long Qt Syndrome 1 55 0.067
40
P LFT003 Left Ventricular Noncompaction 46 0.067
41
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 45 0.067
42
CRD137 Cardiogenic Shock 42 0.067
43
HYP017 Hypophosphatemia 42 0.067
44
CRB009 Cerebritis 33 0.067
45
SYS003 Systolic Heart Failure 31 0.067
46
DCH001 Duchenne Muscular Dystrophy 78 0.058
47
P CRN211 Coronary Artery Disease 73 0.058
48
P SDD001 Sudden Infant Death Syndrome 62 0.058
49
CST001 Costello Syndrome 59 0.058
50
c SYS005 Systemic Scleroderma 58 0.058
51
BRT005 Barth Syndrome 58 0.058
52
P HYP076 Hyperthyroidism 54 0.058
53
CHG001 Chagas Disease 54 0.058
54
PLY041 Polymyositis 51 0.058
55
P EMR001 Emery-Dreifuss Muscular Dystrophy 51 0.058
56
P OCL013 Oculodentodigital Dysplasia 49 0.058
57
P TMT001 Timothy Syndrome 48 0.058
58
P JRV003 Jervell and Lange-Nielsen Syndrome 46 0.058
59
ATR057 Atrioventricular Block 44 0.058
60
P THY054 Thyrotoxic Periodic Paralysis 43 0.058
61
c ACT076 Acute Myocarditis 40 0.058
62
P MCR260 Microphthalmia, Syndromic 7 40 0.058
63
c SHR030 Short Qt Syndrome 39 0.058
64
P TRC086 Trichohepatoenteric Syndrome 1 39 0.058
65
CRP018 Cor Pulmonale 37 0.058
66
CRN030 Coronary Stenosis 36 0.058
67
GNT019 Giant Cell Myocarditis 33 0.058
68
INF013 Inferior Myocardial Infarction 33 0.058
69
RGH001 Right Bundle Branch Block 31 0.058
70
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 30 0.058
71
c LNG092 Long Qt Syndrome-3 29 0.058
72
P CRD132 Cardiac Conduction Defect 28 0.058
73
c LNG053 Long Qt Syndrome 9 27 0.058
74
SPN148 Spondylometaphyseal Dysplasia Sedaghatian Type 21 0.058
75
HSB001 His Bundle Tachycardia 17 0.058
76
P HMC003 Hemochromatosis 75 0.047
77
ACR007 Acromegaly 69 0.047
78
P TBR001 Tuberous Sclerosis 68 0.047
79
PRP083 Porphyria, Acute Intermittent 67 0.047
80
P LPR002 Leopard Syndrome 67 0.047
81
P NNN008 Noonan Syndrome 1 66 0.047
82
P DMN001 Diamond-Blackfan Anemia 66 0.047
83
KWS002 Kawasaki Disease 66 0.047
84
P HLP001 Holoprosencephaly 65 0.047
85
VNH007 Von Hippel-Lindau Syndrome 65 0.047
86
RLP001 Relapsing Polychondritis 63 0.047
87
P DRM010 Dermatomyositis 62 0.047
88
P RSP003 Respiratory Failure 62 0.047
89
PLY017 Polyarteritis Nodosa 60 0.047
90
c FML058 Familial Dilated Cardiomyopathy 59 0.047
91
P SMP003 Simpson-Golabi-Behmel Syndrome 58 0.047
92
P SPN046 Spinal Muscular Atrophy 57 0.047
93
WGN006 Wegener Granulomatosis 57 0.047
94
LYM017 Lyme Disease 56 0.047
95
c DYS166 Dysautonomia, Familial 56 0.047
96
RHM001 Rheumatic Fever 55 0.047
97
SPN186 Spinal Cord Injury 54 0.047
98
c GLY008 Glycogen Storage Disease Ii 54 0.047
99
P LDD002 Liddle Syndrome 52 0.047
100
P PLY019 Polyneuropathy 52 0.047
101
BTL001 Botulism 52 0.047
102
PTN001 Patent Foramen Ovale 52 0.047
103
HMR004 Hemorrhagic Fever with Renal Syndrome 51 0.047
104
P FML161 Familial Mediterranean Fever, Ar 51 0.047
105
P STC001 Stickler Syndrome 51 0.047
106
c SCN006 Secondary Syphilis 51 0.047
107
P HYP192 Hypocalcemia, Autosomal Dominant 50 0.047
108
P SLP006 Sleep Apnea 50 0.047
109
PTN002 Patent Ductus Arteriosus 49 0.047
110
c MLT024 Multiple Endocrine Neoplasia Iia 49 0.047
111
PRC012 Pericardial Effusion 49 0.047
112
MCR088 Microscopic Polyangiitis 49 0.047
113
SNS001 Sensorineural Hearing Loss 48 0.047
114
PRP084 Propionicacidemia 48 0.047
115
LGN002 Legionellosis 47 0.047
116
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 47 0.047
117
HYP037 Hyperhomocysteinemia 45 0.047
118
THR013 Thoracic Outlet Syndrome 45 0.047
119
P MSC003 Muscular Atrophy 44 0.047
120
MTR046 Maternally Inherited Diabetes and Deafness 44 0.047
121
CHL028 Childhood Type Dermatomyositis 43 0.047
122
MYC005 Myocardial Stunning 43 0.047
123
CRN055 Carney Triad 43 0.047
124
OBS006 Obstructive Lung Disease 43 0.047
125
c EHL055 Ehlers-Danlos Syndrome, Type Iii 43 0.047
126
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 43 0.047
127
ATX019 Ataxia with Vitamin E Deficiency 42 0.047
128
CCN002 Cocaine Abuse 42 0.047
129
c PRX045 Peroxisome Biogenesis Disorder 1b 42 0.047
130
P CNG018 Congenital Heart Block 42 0.047
131
P SPL037 Split Hand Foot Malformation 41 0.047
132
CRN041 Carnitine-Acylcarnitine Translocase Deficiency 41 0.047
133
P HYP599 Hypoparathyroidism, Familial Isolated 39 0.047
134
ATN005 Autonomic Dysfunction 39 0.047
135
DXT001 Dextrocardia 37 0.047
136
LYM029 Lymphedema-Distichiasis Syndrome 37 0.047
137
FCL014 Focal Epilepsy 37 0.047
138
PRP009 Peripartum Cardiomyopathy 37 0.047
139
STR037 Stress Cardiomyopathy 35 0.047
140
P KLF001 Kleefstra Syndrome 35 0.047
141
PHC013 Phaeochromocytoma 34 0.047
142
SCH068 Schwartz-Jampel Syndrome, Type 1 34 0.047
143
SPR099 Supravalvar Aortic Stenosis 34 0.047
144
ATY013 Atypical Rett Syndrome 34 0.047
145
c CTS034 Cutis Laxa, Autosomal Recessive Type 1 32 0.047
146
c LNG047 Long Qt Syndrome 2 32 0.047
147
MGL023 Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome, Somatic 30 0.047
148
c FML250 Familial Progressive Cardiac Conduction Defect 29 0.047
149
ANG060 Angiopathy, Hereditary, with Nephropathy, Aneurysms, and Muscle Cramps 26 0.047
150
P PHC014 Phocomelia 25 0.047
151
c LNG050 Long Qt Syndrome 5 23 0.047
152
WRM004 Warm Antibody Hemolytic Anemia 23 0.047
153
c CRD093 Cardiomyopathy, Dilated, 1a 23 0.047
154
CPL011 Capillary Malformations, Congenital, 1, Somatic, Mosaic 23 0.047
155
GST007 Gastric Dilatation 23 0.047
156
c LNG051 Long Qt Syndrome 6 21 0.047
157
SHP003 Shapiro Syndrome 20 0.047
158
c LNG057 Long Qt Syndrome 13 20 0.047
159
MXD035 Mixed-Type Autoimmune Hemolytic Anemia 20 0.047
160
BRC019 Brachycephalofrontonasal Dysplasia 19 0.047
161
DRG014 Drug-Induced Autoimmune Hemolytic Anemia 19 0.047
162
NRL019 Neurologic Waardenburg-Shah Syndrome 19 0.047
163
EHL059 Ehlers-Danlos Syndrome Due to Tenascin-X Deficiency 18 0.047
164
c CNG420 Congenital Muscular Dystrophy Due to Lmna Mutation 18 0.047
165
TBT001 Tabatznik Syndrome 18 0.047
166
TRT006 Torticollis Keloids Cryptorchidism Renal Dysplasia 17 0.047
167
CRD023 Cardiomyopathy Cataract Hip Spine Disease 17 0.047
168
DFN007 Deafness Enamel Hypoplasia Nail Defects 17 0.047
169
c LNG093 Long Qt Syndrome-11 17 0.047
170
MTC105 Mitochondrial Encephalo-Cardio-Myopathy Due to Tmem70 Deficiency 16 0.047
171
SCN049 Second-Degree Atrioventricular Block 16 0.047
172
NTH002 Nathalie Syndrome 16 0.047
173
c LNG056 Long Qt Syndrome 12 16 0.047
174
19P001 19p13.12 Microdeletion Syndrome 16 0.047
175
c VNT013 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1 15 0.047
176
WLL009 Woolly Hair Hypotrichosis Everted Lower Lip and Outstanding Ears 15 0.047
177
CRN253 Carnitine Palmitoyl Transferase Ii Deficiency, Neonatal Form 15 0.047
178
c CRD152 Cardiomyopathy, Familial Hypertrophic, 21 15 0.047
179
PLY042 Polyneuropathy Mental Retardation Acromicria Premature Menopause 14 0.047
180
CRN252 Carnitine Palmitoyl Transferase Ii Deficiency, Severe Infantile Form 14 0.047
181
VNT005 Ventricular Extrasystoles with Syncopal Episodes - Perodactyly - Robin Sequence 14 0.047
182
16P006 16p11.2p12.2 Microdeletion Syndrome 14 0.047
183
ECT023 Ectodermal Dysplasia, Hidrotic, Christianson-Fourie Type 13 0.047
184
SBR006 Subaortic Stenosis Short Stature Syndrome 13 0.047
185
CNG288 Congenital Absence of Upper Arm and Forearm with Hand Present 13 0.047
186
EXT038 Extrasystoles Short Stature Hyperpigmentation Microcephaly 12 0.047
187
HRS003 Hirschsprung Disease Ganglioneuroblastoma 12 0.047
188
c FML196 Familial Isolated Hypoparathyroidism Due to Agenesis of Parathyroid Gland 12 0.047
189
MSC030 Muscular Fibrosis Multifocal Obstructed Vessels 11 0.047
190
P PLM037 Pulmonary Hypertension 85 0.033
191
c AMY091 Amyotrophic Lateral Sclerosis 1 82 0.033
192
MRF001 Marfan Syndrome 75 0.033
193
CDS001 Cadasil 73 0.033
194
P WSK001 Wiskott-Aldrich Syndrome 69 0.033
195
P RBN001 Rubinstein-Taybi Syndrome 67 0.033
196
LVR012 Liver Cirrhosis 66 0.033
197
P BPL003 Bipolar Disorder 65 0.033
198
MGR002 Migraine 64 0.033
199
P AMY004 Amyloidosis 63 0.033
200
ASP006 Aspergillosis 63 0.033
201
P MTH008 Methylmalonic Acidemia 63 0.033
202
P TMP003 Temporal Arteritis 62 0.033
203
BCK001 Becker Muscular Dystrophy 61 0.033
204
P MST009 Mastocytosis 61 0.033
205
P HYP055 Hypoplastic Left Heart Syndrome 61 0.033
206
c CNG006 Congenital Hypothyroidism 61 0.033
207
PRP027 Peripheral Vascular Disease 60 0.033
208
ANX002 Anxiety Disorder 60 0.033
209
VSC007 Vascular Disease 59 0.033
210
c PRM005 Primary Hyperparathyroidism 58 0.033
211
P MNN013 Meningitis 58 0.033
212
ART021 Arteriosclerosis 58 0.033
213
P HYP004 Hypercalcemia 57 0.033
214
c ATM010 Autoimmune Hemolytic Anemia 57 0.033
215
P HYP069 Hyperparathyroidism 57 0.033
216
END030 End Stage Renal Failure 56 0.033
217
ATH003 Atherosclerosis 56 0.033
218
P HLT001 Holt-Oram Syndrome 56 0.033
219
LBR002 Leber Hereditary Optic Neuropathy 55 0.033
220
ART111 Artery Disease 55 0.033
221
CRN183 Carnitine Palmitoyltransferase Ii Deficiency 54 0.033
222
P ACR001 Aicardi-Goutieres Syndrome 54 0.033
223
TYP007 Typhoid Fever 53 0.033
224
HYP056 Hypoglycemia 53 0.033
225
P MYP004 Myopathy 53 0.033
226
KRN002 Kearns-Sayre Syndrome 52 0.033
227
P MTR012 Mitral Valve Disease 52 0.033
228
DNN001 Danon Disease 52 0.033
229
P LMB006 Limb-Girdle Muscular Dystrophy 52 0.033
230
STT002 Status Asthmaticus 52 0.033
231
ISC006 Ischemic Heart Disease 51 0.033
232
c LCL006 Localized Scleroderma 51 0.033
233
P BRT004 Bartter Disease 51 0.033
234
P MYP101 Myopathy, Centronuclear 50 0.033
235
YLL002 Yellow Fever 50 0.033
236
CHL068 Cholestasis 50 0.033
237
CRN017 Coronary Thrombosis 50 0.033
238
CNN005 Connective Tissue Disease 50 0.033
239
CND002 Conduct Disorder 50 0.033
240
P MLS001 Melas Syndrome 50 0.033
241
LPD010 Lipodystrophy 49 0.033
242
HYP266 Hypoxia 49 0.033
243
THY033 Thyrotoxicosis 49 0.033
244
P CRV039 Cervicitis 49 0.033
245
TNS005 Tonsillitis 48 0.033
246
ANH002 Anhidrosis 48 0.033
247
P SYP003 Syphilis 48 0.033
248
c SPN225 Spondyloarthropathy 1 48 0.033
249
P END033 Endocarditis 48 0.033
250
HTR003 Heterotaxy 48 0.033
251
DDN006 Duodenitis 48 0.033
252
P PSD015 Pseudohypoparathyroidism 47 0.033
253
c MYT021 Myotonic Dystrophy 1 47 0.033
254
MTN003 Motion Sickness 47 0.033
255
ULN003 Ulnar-Mammary Syndrome 47 0.033
256
CRD001 Cardiac Tamponade 46 0.033
257
GST037 Gastroparesis 46 0.033
258
EBS001 Ebstein Anomaly 46 0.033
259
AGG002 Aggressive Systemic Mastocytosis 45 0.033
260
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 45 0.033
261
P RST002 Restrictive Cardiomyopathy 45 0.033
262
IMP005 Impotence 45 0.033
263
END072 Endotheliitis 44 0.033
264
INV001 Invasive Aspergillosis 44 0.033
265
TRN015 Transient Cerebral Ischemia 44 0.033
266
P DYS021 Dysautonomia 44 0.033
267
MCR103 Microtia 44 0.033
268
c CNG012 Congenital Generalized Lipodystrophy 43 0.033
269
ANG054 Angina Pectoris 43 0.033
270
P PHS004 Phosphoribosylpyrophosphate Synthetase Superactivity 43 0.033
271
FBR047 Fibromyalgia 42 0.033
272
P PSD003 Pseudohypoaldosteronism 42 0.033
273
P NRV007 Nervous System Disease 42 0.033
274
END021 Endomyocardial Fibrosis 42 0.033
275
AGR002 Agoraphobia 42 0.033
276
NXS001 Naxos Disease 42 0.033
277
c CNT035 Central Nervous System Disease 42 0.033
278
TRY001 Trypanosomiasis 42 0.033
279
c CNT015 Central Sleep Apnea 42 0.033
280
BRN106 Burns 42 0.033
281
DRG003 Drug Dependence 41 0.033
282
ALC010 Alcoholic Cardiomyopathy 41 0.033
283
c CRD099 Cardiomyopathy, Dilated, 1e 41 0.033
284
P MYF003 Myofibrillar Myopathy 40 0.033
285
c MYT020 Myotonic Dystrophy 2 40 0.033
286
ESN011 Eisenmenger Syndrome 40 0.033
287
CRT008 Carotid Artery Dissection 40 0.033
288
FTT003 Fatty Acid Oxidation Disorders 39 0.033
289
EVN001 Evans' Syndrome 39 0.033
290
PLM068 Pulmonary Vein Stenosis 39 0.033
291
CTS011 Cutis Marmorata Telangiectatica Congenita 39 0.033
292
PNN001 Panniculitis 38 0.033
293
ART004 Aortic Atherosclerosis 38 0.033
294
INF034 Infective Endocarditis 38 0.033
295
TRN012 Transient Global Amnesia 37 0.033
296
NRN002 Neuronitis 36 0.033
297
CRB004 Cerebral Artery Occlusion 36 0.033
298
HYP022 Hypohidrosis 36 0.033
299
c EMR011 Emery-Dreifuss Muscular Dystrophy 2, Ad 36 0.033
300
MYT022 Myotubular Myopathy, X-Linked 36 0.033
301
SPL040 Split Hand 35 0.033
302
ESN020 Eosinophilic Granulomatosis with Polyangiitis 35 0.033
303
c CCK005 Cockayne Syndrome, Type a 34 0.033
304
c CCK006 Cockayne Syndrome, Type B 34 0.033
305
c MLG132 Malignant Hyperthermia Susceptibility 1 33 0.033
306
TRC062 Tricuspid Atresia 33 0.033
307
c SYS007 Systemic Capillary Leak Syndrome 32 0.033
308
BRN055 Bronchogenic Cyst 32 0.033
309
c ATM022 Autoimmune Myocarditis 32 0.033
310
c DYS170 Dyserythropoietic Anemia, Congenital, Type Ii 32 0.033
311
MNN032 Meningococcal Meningitis 32 0.033
312
HTR014 Heterotaxy, Visceral, 1, X-Linked 32 0.033
313
ADN002 Adenoiditis 31 0.033
314
CGN006 Cogan Syndrome 31 0.033
315
c DYS156 Dyserythropoietic Anemia, Congenital, Type Ia 31 0.033
316
c SMP007 Simpson-Golabi-Behmel Syndrome, Type 1 31 0.033
317
PRN037 Prinzmetal's Variant Angina 29 0.033
318
CPT003 Cpt Deficiency, Hepatic, Type Ia 29 0.033
319
MTC028 Mitochondrial Cardiomyopathy 28 0.033
320
c FML272 Familial Sick Sinus Syndrome 27 0.033
321
DPH006 Diaphragmatic Eventration 27 0.033
322
WDH003 Woodhouse-Sakati Syndrome 27 0.033
323
CNG134 Congenitally Corrected Transposition of the Great Arteries 27 0.033
324
GLS004 Glossopharyngeal Neuralgia 27 0.033
325
IVC001 Ivic Syndrome 26 0.033
326
P EMR004 Emery-Dreifuss Muscular Dystrophy, X-Linked 26 0.033
327
ADT003 Auditory System Disease 26 0.033
328
c MSC112 Muscular Dystrophy, Limb-Girdle, Type 1b 25 0.033
329
c BRG009 Brugada Syndrome 7 25 0.033
330
ARR038 Arrhythmogenic Right Ventricular Dysplasia 11 25 0.033
331
HMN017 Hemangioma Thrombocytopenia Syndrome 24 0.033
332
c CRD100 Cardiomyopathy, Dilated 1c 23 0.033
333
NTR041 N-Terminal Acetyltransferase Deficiency 23 0.033
334
CHR209 Chromosome 17p Duplication 23 0.033
335
SCP009 Scapuloperoneal Myopathy, X-Linked Dominant 22 0.033
336
SDD002 Sudden Infant Death with Dysgenesis of the Testes Syndrome 22 0.033
337
FDB001 Foodborne Botulism 22 0.033
338
c MYP072 Myopathy, Myofibrillar, 1 22 0.033
339
BRC014 Brachydactyly-Mental Retardation Syndrome 21 0.033
340
MYP056 Myopathy, X-Linked, with Postural Muscle Atrophy 21 0.033
341
CRN057 Carnitine Palmitoyltransferase I Deficiency , Muscle 21 0.033
342
c CRD154 Cardiomyopathy, Familial Hypertrophic 6 21 0.033
343
ANT054 Anotia 21 0.033
344
PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 20 0.033
345
c HMC021 Hemochromatosis, Type 2a 20 0.033
346
RGH009 Right Atrial Isomerism 20 0.033
347
KNN003 Kennerknecht Vogel Syndrome 20 0.033
348
ARR035 Arrhythmogenic Right Ventricular Dysplasia 9 19 0.033
349
LWN001 Lown-Ganong-Levine Syndrome 19 0.033
350
c CRD107 Cardiomyopathy, Dilated, 1r 19 0.033
351
CPT005 Cpt Ii Deficiency, Lethal Neonatal 19 0.033
352
ARR030 Arrhythmogenic Right Ventricular Dysplasia 2 19 0.033
353
c EMR017 Emery-Dreifuss Muscular Dystrophy 1, X-Linked 18 0.033
354
MYP092 Myopathy, Early-Onset, with Fatal Cardiomyopathy 18 0.033
355
MCL055 Mcleod Syndrome with or Without Chronic Granulomatous Disease 18 0.033
356
c GLY009 Glycogen Storage Disease Xv 18 0.033
357
c VNT024 Ventricular Septal Defect 3 18 0.033
358
c VNT028 Ventricular Septal Defect 1 17 0.033
359
ARR026 Arrhythmogenic Right Ventricular Dysplasia 1 17 0.033
360
c BRG003 Brugada Syndrome 3 17 0.033
361
DMD003 Dmd-Associated Dilated Cardiomyopathy 17 0.033
362
LFT013 Left Ventricular Noncompaction 1, with or Without Congenital Heart Defects 17 0.033
363
c CRD056 Cardiomyopathy, Familial Hypertrophic, 11 17 0.033
364
c CRD104 Cardiomyopathy, Dilated, 1p 17 0.033
365
HCS001 Hec Syndrome 17 0.033
366
CMB025 Combined Oxidative Phosphorylation Deficiency 10 17 0.033
367
c EMR003 Emery-Dreifuss Muscular Dystrophy, Dominant Type 16 0.033
368
P HRT017 Heart Tumor 16 0.033
369
BSL014 Basilar Migraine 16 0.033
370
KNS002 Kniest Like Dysplasia Lethal 16 0.033
371
END052 Endomyocardial Fibroelastosis 15 0.033
372
DXR001 Doxorubicin Induced Cardiomyopathy 15 0.033
373
c EMR015 Emery-Dreifuss Muscular Dystrophy 5, Autosomal Dominant 15 0.033
374
HRT019 Heart-Hand Syndrome,spanish Type 14 0.033
375
MTC078 Mitochondrial Dna Depletion Syndrome 11 14 0.033
376
MTC088 Mitochondrial Dna Depletion Syndrome 13 14 0.033
377
RBB001 Ribbing Disease 13 0.033
378
c LFT017 Left Ventricular Noncompaction 8 13 0.033
379
BRC025 Brachydactyly Long Thumb Type 13 0.033
380
THL007 Thalamic Degeneration Symmetrical Infantile 13 0.033
381
c VNT026 Ventricular Septal Defect 2 13 0.033
382
PLY088 Polyvalvular Heart Disease Syndrome 13 0.033
383
c CRD173 Cardiomyopathy, Dilated, 1nn 12 0.033
384
MTC068 Mitochondrial Complex V Deficiency, Nuclear Type 2 12 0.033
385
DGT004 Digitalis Poisoning 12 0.033
386
INT062 Interstitial Myocarditis 11 0.033
387
RTN072 Retinohepatoendocrinologic Syndrome 11 0.033
388
TXC010 Toxic Myocarditis 11 0.033
389
SBN001 Subendocardial Myocardial Infarction 10 0.033
390
ANR042 Aniridia - Ptosis - Intellectual Disability - Familial Obesity 10 0.033
391
ARR041 Arrhythmogenic Right Ventricular Dysplasia, Familial, 13 10 0.033
392
ATR080 Atrial Septal Defect - Atrioventricular Conduction Defects 9 0.033
393
CRN208 Coronary Sinus Atresia 8 0.033
394
SNS012 Sinus Node Disease and Myopia 5 0.033