Search results for "arrhythmia"

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

416 hits were found for 'arrhythmia'

# Family MCID Name MIFTS Score
1
PHC009 Phocomelia Ectrodactyly Deafness Sinus Arrhythmia 20 4.691
2
WLF001 Wolff-Parkinson-White Syndrome 74 3.416
3
SDD004 Sudden Arrhythmia Death Syndrome 13 3.364
4
PHC010 Phocomelia-Ectrodactyly Ear Malformation Deafness and Sinus Arrhythmia 4 3.309
5
CRD054 Cardiac Arrhythmia, Ankyrin-B-Related 7 3.270
6
OGD001 Ogden Syndrome 24 2.312
7
P MYC007 Myocardial Infarction 92 0.187
8
c LNG028 Long Qt Syndrome 64 0.187
9
c BRG001 Brugada Syndrome 58 0.137
10
P MTR005 Mitral Valve Prolapse 59 0.133
11
c ACT075 Acute Myocardial Infarction 59 0.133
12
c CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 56 0.133
13
P DLT002 Dilated Cardiomyopathy 87 0.128
14
c SCK002 Sick Sinus Syndrome 57 0.124
15
AND003 Andersen-Tawil Syndrome 53 0.119
16
P HYP075 Hypertension 85 0.110
17
P SRC013 Sarcoidosis 73 0.110
18
c HYP061 Hypertrophic Cardiomyopathy 64 0.110
19
HYP005 Hypokalemia 49 0.110
20
SYN036 Syncope 44 0.110
21
CRD003 Cardiac Sarcoidosis 51 0.105
22
ISC004 Ischemia 62 0.099
23
c MYT002 Myotonic Dystrophy 61 0.099
24
P MYC008 Myocarditis 57 0.094
25
CNG034 Congestive Heart Failure 77 0.088
26
TTR001 Tetralogy of Fallot 74 0.088
27
P LNG044 Long Qt Syndrome 1 68 0.088
28
TRN044 Transposition of the Great Arteries 49 0.088
29
ANR040 Aneurysm 45 0.088
30
c HYP051 Hypokalemic Periodic Paralysis 61 0.081
31
P MYT006 Myotonic Dystrophy Type 1 61 0.081
32
NRP001 Neuropathy 61 0.081
33
c ATN004 Autonomic Neuropathy 49 0.081
34
ATR055 Atrial Septal Aneurysm 22 0.081
35
SPS077 Sepsis 69 0.074
36
P SYS005 Systemic Scleroderma 66 0.074
37
HYP006 Hypertensive Heart Disease 49 0.074
38
DBT002 Diabetic Autonomic Neuropathy 48 0.074
39
FBR012 Fabry Disease 85 0.066
40
P RFS001 Refsum Disease 77 0.066
41
P FML032 Familial Hypertrophic Cardiomyopathy 68 0.066
42
c MSC005 Muscular Dystrophy 61 0.066
43
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 56 0.066
44
P JRV001 Jervell-Lange Nielsen Syndrome 51 0.066
45
HYP017 Hypophosphatemia 48 0.066
46
CRD137 Cardiogenic Shock 48 0.066
47
c LFT003 Left Ventricular Noncompaction 42 0.066
48
SYS003 Systolic Heart Failure 37 0.066
49
CPT005 Cpt Ii Deficiency, Lethal Neonatal 29 0.066
50
SPN148 Spondylometaphyseal Dysplasia Sedaghatian Type 27 0.066
51
P RTT002 Rett Syndrome 83 0.057
52
P SDD001 Sudden Infant Death Syndrome 71 0.057
53
P CNG401 Congenital Heart Disease 69 0.057
54
BRT005 Barth Syndrome 66 0.057
55
CST001 Costello Syndrome 66 0.057
56
c HYP076 Hyperthyroidism 62 0.057
57
PLY041 Polymyositis 58 0.057
58
P OCL013 Oculodentodigital Dysplasia 56 0.057
59
P TMT001 Timothy Syndrome 55 0.057
60
ATR057 Atrioventricular Block 52 0.057
61
c ACT076 Acute Myocarditis 47 0.057
62
c SHR030 Short Qt Syndrome 47 0.057
63
c THY054 Thyrotoxic Periodic Paralysis 46 0.057
64
LYM029 Lymphedema-Distichiasis Syndrome 45 0.057
65
CRP018 Cor Pulmonale 44 0.057
66
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 43 0.057
67
CRN030 Coronary Stenosis 43 0.057
68
P VNT013 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1 41 0.057
69
INF013 Inferior Myocardial Infarction 40 0.057
70
CRB009 Cerebritis 38 0.057
71
GNT019 Giant Cell Myocarditis 38 0.057
72
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 33 0.057
73
c LNG053 Long Qt Syndrome 9 28 0.057
74
c CRD132 Cardiac Conduction Defect 27 0.057
75
MTC068 Mitochondrial Complex V Deficiency, Nuclear Type 2 23 0.057
76
HSB001 His Bundle Tachycardia 19 0.057
77
P TBR001 Tuberous Sclerosis 86 0.047
78
P HMC003 Hemochromatosis 85 0.047
79
VNH001 Von Hippel-Lindau Disease 81 0.047
80
ACR007 Acromegaly 79 0.047
81
ACT033 Acute Intermittent Porphyria 78 0.047
82
DCH001 Duchenne Muscular Dystrophy 77 0.047
83
KWS002 Kawasaki Disease 75 0.047
84
P THY014 Thyroid Medullary Carcinoma 73 0.047
85
P WGN002 Wegener's Granulomatosis 73 0.047
86
P PRP001 Propionic Acidemia 72 0.047
87
RLP001 Relapsing Polychondritis 72 0.047
88
P DRM010 Dermatomyositis 71 0.047
89
PLY017 Polyarteritis Nodosa 69 0.047
90
P RSP003 Respiratory Failure 68 0.047
91
P NNN008 Noonan Syndrome 1 68 0.047
92
P CNG030 Congenital Muscular Dystrophy 67 0.047
93
P EPL025 Epileptic Encephalopathy, Early Infantile, 2 67 0.047
94
RHM001 Rheumatic Fever 66 0.047
95
c SPN046 Spinal Muscular Atrophy 65 0.047
96
P CRN018 Coronary Artery Anomaly 65 0.047
97
LYM017 Lyme Disease 65 0.047
98
c SCL016 Scleroderma 64 0.047
99
CHG001 Chagas Disease 62 0.047
100
P GLY008 Glycogen Storage Disease Ii 62 0.047
101
SPN186 Spinal Cord Injury 61 0.047
102
HMR004 Hemorrhagic Fever with Renal Syndrome 61 0.047
103
PTN001 Patent Foramen Ovale 61 0.047
104
BTL001 Botulism 60 0.047
105
MTR046 Maternally Inherited Diabetes and Deafness 60 0.047
106
P PLY019 Polyneuropathy 60 0.047
107
c SLP006 Sleep Apnea 59 0.047
108
RLY001 Riley-Day Syndrome 58 0.047
109
PRC012 Pericardial Effusion 57 0.047
110
PTN002 Patent Ductus Arteriosus 57 0.047
111
SNS001 Sensorineural Hearing Loss 57 0.047
112
SCN006 Secondary Syphilis 56 0.047
113
P HLP012 Holoprosencephaly-3 56 0.047
114
MCR088 Microscopic Polyangiitis 56 0.047
115
c LPR012 Leopard Syndrome 1 55 0.047
116
P STC005 Stickler Syndrome Type 1 55 0.047
117
LGN002 Legionellosis 55 0.047
118
SPR004 Supravalvular Aortic Stenosis 54 0.047
119
P LDD002 Liddle Syndrome 54 0.047
120
P HYP192 Hypocalcemia, Autosomal Dominant 54 0.047
121
P MSC003 Muscular Atrophy 53 0.047
122
HYP037 Hyperhomocysteinemia 52 0.047
123
OBS006 Obstructive Lung Disease 52 0.047
124
MYC005 Myocardial Stunning 51 0.047
125
CRN055 Carney Triad 50 0.047
126
ATX019 Ataxia with Vitamin E Deficiency 50 0.047
127
c EMR001 Emery-Dreifuss Muscular Dystrophy 50 0.047
128
CCN002 Cocaine Abuse 50 0.047
129
c CNG018 Congenital Heart Block 50 0.047
130
P EHL034 Ehlers-Danlos Syndrome, Hypermobility Type 49 0.047
131
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 49 0.047
132
P ATN005 Autonomic Dysfunction 46 0.047
133
P DMN023 Diamond-Blackfan Anemia 1 46 0.047
134
CRN041 Carnitine-Acylcarnitine Translocase Deficiency 46 0.047
135
FCL014 Focal Epilepsy 46 0.047
136
P MYH004 Myh9 Related Thrombocytopenia 46 0.047
137
MYP019 Myopathy with Postural Muscle Atrophy, X-Linked 45 0.047
138
c HYP052 Hyperkalemic Periodic Paralysis 45 0.047
139
P SMP004 Simpson-Golabi-Behmel Syndrome Type 1 44 0.047
140
P HYP216 Hypoparathyroidism Familial Isolated 44 0.047
141
PRP009 Peripartum Cardiomyopathy 43 0.047
142
DXT001 Dextrocardia 43 0.047
143
c FML058 Familial Dilated Cardiomyopathy 42 0.047
144
P SPL033 Split-Hand/foot Malformation 6 42 0.047
145
PHC013 Phaeochromocytoma 42 0.047
146
P PRX064 Peroxisome Biogenesis Disorder 2b 42 0.047
147
P HRT021 Heart Block, Progressive, Type Ia 41 0.047
148
STR037 Stress Cardiomyopathy 40 0.047
149
P KLF001 Kleefstra Syndrome 40 0.047
150
P SCH035 Schwartz Jampel Syndrome Type 1 39 0.047
151
c FML162 Familial Mediterranean Fever, Ad 37 0.047
152
RGH001 Right Bundle Branch Block 36 0.047
153
c CTS030 Cutis Laxa, Autosomal Recessive, Type Ia 36 0.047
154
PHN011 Phenytoin Toxicity 35 0.047
155
c SPL037 Split Hand Foot Malformation 35 0.047
156
P HYP239 Hyperkalemic Periodic Paralysis Type 2 33 0.047
157
c LNG048 Long Qt Syndrome 3 32 0.047
158
MGL023 Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome, Somatic 31 0.047
159
CHL028 Childhood Type Dermatomyositis 31 0.047
160
c LNG047 Long Qt Syndrome 2 30 0.047
161
APL022 Aplasia Cutis Congenita, Reticulolinear, with Mmicrocephaly, Facial Dysmorphism and Other Congenital Anomalies 30 0.047
162
HRD040 Hereditary Angiopathy with Nephropathy, Aneurysms, and Muscle Cramps Syndrome 30 0.047
163
c PHC014 Phocomelia 29 0.047
164
HYP203 Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extrapyramidal Syndrome 29 0.047
165
GST007 Gastric Dilatation 28 0.047
166
CPL011 Capillary Malformations, Congenital, 1, Somatic, Mosaic 26 0.047
167
PCW002 Pcwh Syndrome 26 0.047
168
CPT003 Cpt Deficiency, Hepatic, Type Ia 25 0.047
169
c LNG050 Long Qt Syndrome 5 24 0.047
170
EHL044 Ehlers-Danlos Syndrome, Autosomal Recessive, Due to Tenascin X Deficiency 23 0.047
171
BRC019 Brachycephalofrontonasal Dysplasia 23 0.047
172
DRG014 Drug-Induced Autoimmune Hemolytic Anemia 22 0.047
173
TRT006 Torticollis Keloids Cryptorchidism Renal Dysplasia 22 0.047
174
c LNG051 Long Qt Syndrome 6 21 0.047
175
TBT001 Tabatznik Syndrome 21 0.047
176
SHP003 Shapiro Syndrome 21 0.047
177
MXD035 Mixed-Type Autoimmune Hemolytic Anemia 21 0.047
178
DFN007 Deafness Enamel Hypoplasia Nail Defects 21 0.047
179
c LNG057 Long Qt Syndrome 13 20 0.047
180
SCN049 Second-Degree Atrioventricular Block 20 0.047
181
KNS002 Kniest Like Dysplasia Lethal 19 0.047
182
NTH002 Nathalie Syndrome 19 0.047
183
CPT004 Cpt Deficiency, Hepatic, Type Ii 19 0.047
184
16P006 16p11.2p12.2 Microdeletion Syndrome 19 0.047
185
c LNG049 Long Qt Syndrome 4 19 0.047
186
ATM069 Autoimmune Hemolytic Anemia, Warm Type 18 0.047
187
WLL009 Woolly Hair Hypotrichosis Everted Lower Lip and Outstanding Ears 18 0.047
188
CRD023 Cardiomyopathy Cataract Hip Spine Disease 18 0.047
189
c CRD093 Cardiomyopathy, Dilated, 1a 18 0.047
190
SBR006 Subaortic Stenosis Short Stature Syndrome 17 0.047
191
c LNG046 Long Qt Syndrome 11 17 0.047
192
P 19P001 19p13.12 Microdeletion Syndrome 17 0.047
193
c LNG056 Long Qt Syndrome 12 17 0.047
194
ECT023 Ectodermal Dysplasia, Hidrotic, Christianson-Fourie Type 16 0.047
195
HRS003 Hirschsprung Disease Ganglioneuroblastoma 15 0.047
196
c FML196 Familial Isolated Hypoparathyroidism Due to Agenesis of Parathyroid Gland 15 0.047
197
EXT038 Extrasystoles Short Stature Hyperpigmentation Microcephaly 15 0.047
198
CNG288 Congenital Absence of Upper Arm and Forearm with Hand Present 14 0.047
199
PLY106 Polyneuropathy - Intellectual Disability - Acromicria - Premature Menopause 12 0.047
200
MSC030 Muscular Fibrosis Multifocal Obstructed Vessels 12 0.047
201
P HNT001 Huntington's Disease 87 0.033
202
MRF001 Marfan Syndrome 85 0.033
203
CDS001 Cadasil 84 0.033
204
AND002 Androgen Insensitivity Syndrome 80 0.033
205
P PRM021 Primary Pulmonary Hypertension 80 0.033
206
P WSK001 Wiskott-Aldrich Syndrome 79 0.033
207
P MTH008 Methylmalonic Acidemia 79 0.033
208
P RBN001 Rubinstein-Taybi Syndrome 77 0.033
209
P BPL003 Bipolar Disorder 76 0.033
210
ANK002 Ankylosing Spondylitis 76 0.033
211
P MST009 Mastocytosis 75 0.033
212
c ESS002 Essential Hypertension 73 0.033
213
P AMY004 Amyloidosis 73 0.033
214
c PLM037 Pulmonary Hypertension 73 0.033
215
ASP006 Aspergillosis 72 0.033
216
c HYP095 Hypercholesterolemia 72 0.033
217
P TMP003 Temporal Arteritis 72 0.033
218
P MGR002 Migraine 71 0.033
219
P ANG001 Angelman Syndrome 71 0.033
220
P PRM005 Primary Hyperparathyroidism 70 0.033
221
c AXN002 Axenfeld-Rieger Syndrome 69 0.033
222
c CNG006 Congenital Hypothyroidism 69 0.033
223
VSC007 Vascular Disease 69 0.033
224
P CCK003 Cockayne Syndrome Type Ii 69 0.033
225
ATH003 Atherosclerosis 68 0.033
226
ANX002 Anxiety Disorder 68 0.033
227
ART021 Arteriosclerosis 67 0.033
228
c MNN013 Meningitis 67 0.033
229
PRP027 Peripheral Vascular Disease 67 0.033
230
P CNT004 Centronuclear Myopathy 66 0.033
231
P HYP056 Hypoglycemia 66 0.033
232
P ATM010 Autoimmune Hemolytic Anemia 66 0.033
233
P INS005 Insulin Resistance 64 0.033
234
c HYP069 Hyperparathyroidism 64 0.033
235
HYP004 Hypercalcemia 64 0.033
236
LBR002 Leber Hereditary Optic Neuropathy 64 0.033
237
KRN002 Kearns-Sayre Syndrome 63 0.033
238
ART019 Aortic Valve Stenosis 63 0.033
239
P CNG042 Congenital Central Hypoventilation Syndrome 63 0.033
240
P HLT001 Holt-Oram Syndrome 63 0.033
241
ART111 Artery Disease 63 0.033
242
STT002 Status Asthmaticus 63 0.033
243
BCK001 Becker Muscular Dystrophy 62 0.033
244
TYP007 Typhoid Fever 62 0.033
245
c HYP055 Hypoplastic Left Heart Syndrome 62 0.033
246
P MTR012 Mitral Valve Disease 62 0.033
247
P MYP004 Myopathy 61 0.033
248
c LMB006 Limb-Girdle Muscular Dystrophy 61 0.033
249
P MLS001 Melas Syndrome 60 0.033
250
DNN001 Danon Disease 59 0.033
251
c LCL006 Localized Scleroderma 59 0.033
252
YLL002 Yellow Fever 59 0.033
253
ISC006 Ischemic Heart Disease 58 0.033
254
CND002 Conduct Disorder 58 0.033
255
MYC002 Mycobacterium Avium Complex Disease 58 0.033
256
LPD010 Lipodystrophy 58 0.033
257
CNN005 Connective Tissue Disease 58 0.033
258
CRT002 Cartilage-Hair Hypoplasia 57 0.033
259
END030 End Stage Renal Failure 57 0.033
260
P SYP003 Syphilis 57 0.033
261
P CRV039 Cervicitis 57 0.033
262
c MYT007 Myotonic Dystrophy Type 2 57 0.033
263
THY033 Thyrotoxicosis 57 0.033
264
HYP266 Hypoxia 57 0.033
265
ANH002 Anhidrosis 57 0.033
266
TNS005 Tonsillitis 56 0.033
267
MCR103 Microtia 56 0.033
268
P END033 Endocarditis 56 0.033
269
DDN006 Duodenitis 55 0.033
270
MTN003 Motion Sickness 55 0.033
271
EPD037 Epidermal Nevus 55 0.033
272
EBS001 Ebstein Anomaly 55 0.033
273
CRD001 Cardiac Tamponade 54 0.033
274
c GLY007 Glycogen Storage Disease Iv 54 0.033
275
IMP005 Impotence 54 0.033
276
c PSD015 Pseudohypoparathyroidism 54 0.033
277
c BRT004 Bartter Disease 53 0.033
278
c SMP003 Simpson-Golabi-Behmel Syndrome 53 0.033
279
ULN003 Ulnar-Mammary Syndrome 53 0.033
280
AGG002 Aggressive Systemic Mastocytosis 52 0.033
281
INV001 Invasive Aspergillosis 52 0.033
282
THR013 Thoracic Outlet Syndrome 52 0.033
283
c RST002 Restrictive Cardiomyopathy 52 0.033
284
c CNG012 Congenital Generalized Lipodystrophy 52 0.033
285
TRN015 Transient Cerebral Ischemia 52 0.033
286
c CNT048 Central Hypoventilation Syndrome 52 0.033
287
AGR002 Agoraphobia 50 0.033
288
P MLG090 Malignant Hyperthermia Susceptibility Type 1 50 0.033
289
END072 Endotheliitis 50 0.033
290
c CRD099 Cardiomyopathy, Dilated, 1e 50 0.033
291
GRN037 Granulomatosis with Polyangiitis 50 0.033
292
P MJR001 Major Depressive Disorder 50 0.033
293
P NRV007 Nervous System Disease 49 0.033
294
P CNT015 Central Sleep Apnea 49 0.033
295
BRN106 Burns 49 0.033
296
TRY001 Trypanosomiasis 49 0.033
297
FBR047 Fibromyalgia 49 0.033
298
c PSD003 Pseudohypoaldosteronism 49 0.033
299
DRG003 Drug Dependence 49 0.033
300
ALC010 Alcoholic Cardiomyopathy 49 0.033
301
c CNT035 Central Nervous System Disease 48 0.033
302
P PHS004 Phosphoribosylpyrophosphate Synthetase Superactivity 48 0.033
303
P DYS021 Dysautonomia 48 0.033
304
NXS001 Naxos Disease 48 0.033
305
HTR003 Heterotaxy 47 0.033
306
CRT008 Carotid Artery Dissection 47 0.033
307
FTT003 Fatty Acid Oxidation Disorders 47 0.033
308
END021 Endomyocardial Fibrosis 46 0.033
309
PNN001 Panniculitis 46 0.033
310
CTS011 Cutis Marmorata Telangiectatica Congenita 45 0.033
311
ART004 Aortic Atherosclerosis 45 0.033
312
INF034 Infective Endocarditis 44 0.033
313
P FCS001 Facioscapulohumeral Muscular Dystrophy 44 0.033
314
XLN011 X-Linked Centronuclear Myopathy 44 0.033
315
ESN011 Eisenmenger Syndrome 44 0.033
316
TRN012 Transient Global Amnesia 43 0.033
317
NRN002 Neuronitis 43 0.033
318
HYP022 Hypohidrosis 43 0.033
319
P MYF003 Myofibrillar Myopathy 43 0.033
320
PLM068 Pulmonary Vein Stenosis 40 0.033
321
TRC062 Tricuspid Atresia 39 0.033
322
c CNG045 Congenital Dyserythropoietic Anemia Type I 38 0.033
323
ESN020 Eosinophilic Granulomatosis with Polyangiitis 38 0.033
324
P SYS007 Systemic Capillary Leak Syndrome 38 0.033
325
ADN002 Adenoiditis 37 0.033
326
MNN032 Meningococcal Meningitis 37 0.033
327
P EMR011 Emery-Dreifuss Muscular Dystrophy 2, Ad 37 0.033
328
BRN055 Bronchogenic Cyst 37 0.033
329
P 2Q3002 2q37 Microdeletion Syndrome 36 0.033
330
CGN006 Cogan Syndrome 35 0.033
331
P CNG225 Congenital Dyserythropoietic Anemia Type 2 34 0.033
332
SLH001 Salih Myopathy 34 0.033
333
SYN053 Syndromic Diarrhea 34 0.033
334
DPH006 Diaphragmatic Eventration 33 0.033
335
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 33 0.033
336
c CCK002 Cockayne Syndrome Type I 33 0.033
337
P PRX010 Paroxysmal Ventricular Fibrillation 33 0.033
338
c MCR084 Microphthalmia Syndromic 7 32 0.033
339
MTC028 Mitochondrial Cardiomyopathy 32 0.033
340
AMT004 Amitriptyline Toxicity 32 0.033
341
GLS004 Glossopharyngeal Neuralgia 32 0.033
342
P SCK014 Sick Sinus Syndrome 2 31 0.033
343
c HMC021 Hemochromatosis, Type 2a 31 0.033
344
RGH009 Right Atrial Isomerism 30 0.033
345
ADT003 Auditory System Disease 30 0.033
346
c LMB019 Limb-Girdle Muscular Dystrophy, Type 1b 30 0.033
347
CNG134 Congenitally Corrected Transposition of the Great Arteries 30 0.033
348
PRN037 Prinzmetal's Variant Angina 29 0.033
349
HMN017 Hemangioma Thrombocytopenia Syndrome 29 0.033
350
IVC001 Ivic Syndrome 29 0.033
351
XLN031 X-Linked Visceral Heterotaxy 1 28 0.033
352
c MYC058 Myocardial Infarction 2 27 0.033
353
ANT054 Anotia 26 0.033
354
FDB001 Foodborne Botulism 26 0.033
355
c MYP072 Myopathy, Myofibrillar, 1 25 0.033
356
XLN019 X-Linked Dominant Scapuloperoneal Myopathy 25 0.033
357
ARR026 Arrhythmogenic Right Ventricular Dysplasia 1 25 0.033
358
PGD001 Pagod Syndrome 24 0.033
359
MCL055 Mcleod Syndrome with or Without Chronic Granulomatous Disease 24 0.033
360
LWN001 Lown-Ganong-Levine Syndrome 23 0.033
361
c GLY009 Glycogen Storage Disease Xv 23 0.033
362
SDD002 Sudden Infant Death with Dysgenesis of the Testes Syndrome 22 0.033
363
ART007 Aorta Atresia 22 0.033
364
CMB025 Combined Oxidative Phosphorylation Deficiency 10 22 0.033
365
c BNG076 Benign Exophthalmos Syndrome 22 0.033
366
ODN015 Odontotrichomelic Syndrome 22 0.033
367
c BSL014 Basilar Migraine 21 0.033
368
AND005 Androgen Insensitivity Syndrome, Mild 21 0.033
369
HCS001 Hec Syndrome 20 0.033
370
P HRT017 Heart Tumor 20 0.033
371
DMD003 Dmd-Associated Dilated Cardiomyopathy 20 0.033
372
PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 20 0.033
373
MTC088 Mitochondrial Dna Depletion Syndrome 13 19 0.033
374
ATR063 Atrial Septal Defect 7, with or Without Av Conduction Defects 19 0.033
375
c BRG003 Brugada Syndrome 3 18 0.033
376
HRT027 Heart-Hand Syndrome Type 3 18 0.033
377
c CRD100 Cardiomyopathy, Dilated 1c 18 0.033
378
MTC078 Mitochondrial Dna Depletion Syndrome 11 18 0.033
379
END052 Endomyocardial Fibroelastosis 17 0.033
380
VNT011 Ventricular Fibrillation, Familial, 1 17 0.033
381
c BRG009 Brugada Syndrome 7 17 0.033
382
ARR038 Arrhythmogenic Right Ventricular Dysplasia 11 17 0.033
383
THL007 Thalamic Degeneration Symmetrical Infantile 17 0.033
384
DXR001 Doxorubicin Induced Cardiomyopathy 17 0.033
385
MLT131 Multifocal Atrial Tachycardia 16 0.033
386
RBB001 Ribbing Disease 16 0.033
387
MCR033 Macrocephaly-Capillary Malformation 16 0.033
388
20P001 20p12.3 Microdeletion Syndrome 16 0.033
389
c CRD154 Cardiomyopathy, Familial Hypertrophic 6 16 0.033
390
BRC025 Brachydactyly Long Thumb Type 15 0.033
391
INT062 Interstitial Myocarditis 15 0.033
392
c VNT028 Ventricular Septal Defect 1 15 0.033
393
TXC010 Toxic Myocarditis 15 0.033
394
c VNT024 Ventricular Septal Defect 3 14 0.033
395
SNS012 Sinus Node Disease and Myopia 14 0.033
396
RTN072 Retinohepatoendocrinologic Syndrome 14 0.033
397
c CRD107 Cardiomyopathy, Dilated, 1r 14 0.033
398
PLY088 Polyvalvular Heart Disease Syndrome 14 0.033
399
c VNT026 Ventricular Septal Defect 2 14 0.033
400
c CRD173 Cardiomyopathy, Dilated, 1nn 14 0.033
401
P EMR017 Emery-Dreifuss Muscular Dystrophy 1, X-Linked 13 0.033
402
c CRD104 Cardiomyopathy, Dilated, 1p 13 0.033
403
c CRD056 Cardiomyopathy, Familial Hypertrophic, 11 13 0.033
404
c EMR015 Emery-Dreifuss Muscular Dystrophy 5, Autosomal Dominant 12 0.033
405
SBN001 Subendocardial Myocardial Infarction 12 0.033
406
DGT004 Digitalis Poisoning 12 0.033
407
ARR035 Arrhythmogenic Right Ventricular Dysplasia 9 11 0.033
408
c EMR004 Emery-Dreifuss Muscular Dystrophy, X-Linked 11 0.033
409
c SPN225 Spondyloarthropathy 1 11 0.033
410
c LFT017 Left Ventricular Noncompaction 8 11 0.033
411
LFT013 Left Ventricular Noncompaction 1, with or Without Congenital Heart Defects 11 0.033
412
ANR042 Aniridia - Ptosis - Intellectual Disability - Familial Obesity 10 0.033
413
ARR030 Arrhythmogenic Right Ventricular Dysplasia 2 10 0.033
414
ARR041 Arrhythmogenic Right Ventricular Dysplasia, Familial, 13 9 0.033
415
CRN208 Coronary Sinus Atresia 8 0.033
416
c EMR003 Emery-Dreifuss Muscular Dystrophy, Dominant Type 7 0.033