Search results for "arrhythmia"

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

639 hits were found for 'arrhythmia'

# Family MCID Name MIFTS Score
1
CRD054 Cardiac Arrhythmia, Ankyrin-B-Related 25 3.949
2
PHC009 Phocomelia Ectrodactyly Deafness Sinus Arrhythmia 16 3.243
3
WLF001 Wolff-Parkinson-White Syndrome 60 2.389
4
SDD004 Sudden Arrhythmia Death Syndrome 11 2.373
5
PHC010 Phocomelia-Ectrodactyly Ear Malformation Deafness and Sinus Arrhythmia 4 2.313
6
c CRD099 Cardiomyopathy, Dilated, 1e 45 2.285
7
PRM199 Premature Aging Appearance-Developmental Delay-Cardiac Arrhythmia Syndrome 6 2.285
8
P CRD011 Cardiomyopathy 53 0.218
9
P ATR011 Atrial Fibrillation 55 0.215
10
P MYC007 Myocardial Infarction 76 0.200
11
P CNG401 Congenital Heart Disease 68 0.184
12
c FML001 Familial Atrial Fibrillation 53 0.182
13
P LNG028 Long Qt Syndrome 53 0.171
14
SDD007 Sudden Cardiac Death 36 0.166
15
c CRN175 Coronary Heart Disease 4 9 0.162
16
c CRN172 Coronary Heart Disease 3 9 0.154
17
CRD119 Cardiac Arrest 45 0.152
18
SYN036 Syncope 36 0.141
19
c CRN174 Coronary Heart Disease 2 9 0.139
20
P BRG001 Brugada Syndrome 52 0.133
21
c ACT075 Acute Myocardial Infarction 50 0.133
22
ISC004 Ischemia 47 0.130
23
P CRN211 Coronary Artery Disease 68 0.127
24
CNG034 Congestive Heart Failure 65 0.127
25
c DLT002 Dilated Cardiomyopathy 73 0.124
26
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 52 0.124
27
SNG003 Single Ventricular Heart 14 0.121
28
c CRN178 Coronary Heart Disease 6 10 0.118
29
ISC006 Ischemic Heart Disease 56 0.114
30
P PRX010 Paroxysmal Ventricular Fibrillation 26 0.111
31
P NNN008 Noonan Syndrome 1 62 0.107
32
P SCK002 Sick Sinus Syndrome 42 0.107
33
P HYP061 Hypertrophic Cardiomyopathy 56 0.100
34
HYP005 Hypokalemia 39 0.100
35
CRD003 Cardiac Sarcoidosis 33 0.100
36
FNT004 Fainting 27 0.096
37
P CRN214 Coronary Heart Disease 5 10 0.096
38
STR067 Stroke, Ischemic 68 0.092
39
ATR024 Atrial Fibrillation and Stroke 14 0.092
40
P MSC005 Muscular Dystrophy 52 0.088
41
P MYT002 Myotonic Dystrophy 48 0.088
42
P MYC008 Myocarditis 47 0.088
43
PRN021 Paranasal Sinus Disease 38 0.088
44
NSL022 Nasal Cavity Disease 28 0.088
45
ART111 Artery Disease 48 0.083
46
PRP027 Peripheral Vascular Disease 62 0.078
47
P AND016 Andersen Syndrome 58 0.078
48
ART021 Arteriosclerosis 51 0.078
49
ANR040 Aneurysm 43 0.078
50
TTR001 Tetralogy of Fallot 68 0.073
51
HRT012 Heart Valve Disease 40 0.073
52
CRN030 Coronary Stenosis 40 0.073
53
TRN044 Transposition of the Great Arteries 39 0.073
54
P RTT002 Rett Syndrome 79 0.068
55
P MYP004 Myopathy 50 0.068
56
HYP006 Hypertensive Heart Disease 40 0.068
57
ATR057 Atrioventricular Block 39 0.068
58
SYS003 Systolic Heart Failure 37 0.068
59
P CRD132 Cardiac Conduction Defect 29 0.068
60
ATR055 Atrial Septal Aneurysm 21 0.068
61
c MYC058 Myocardial Infarction 2 19 0.068
62
VSC007 Vascular Disease 55 0.062
63
c LNG044 Long Qt Syndrome 1 53 0.062
64
P NRP001 Neuropathy 48 0.062
65
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 47 0.062
66
P SLP006 Sleep Apnea 46 0.062
67
c ART101 Aortic Valve Disease 2 46 0.062
68
P LFT003 Left Ventricular Noncompaction 44 0.062
69
NTR005 Nutritional Deficiency Disease 41 0.062
70
ATN004 Autonomic Neuropathy 39 0.062
71
VND001 Vein Disease 34 0.062
72
SKN023 Skin Tag 33 0.062
73
DBT002 Diabetic Autonomic Neuropathy 31 0.062
74
c CRN173 Coronary Heart Disease 8 9 0.062
75
DCH001 Duchenne Muscular Dystrophy 78 0.055
76
FBR012 Fabry Disease 75 0.055
77
P SCL016 Scleroderma 69 0.055
78
c SPN225 Spondyloarthropathy 1 66 0.055
79
P RFS001 Refsum Disease 65 0.055
80
c MYT021 Myotonic Dystrophy 1 58 0.055
81
c CRD194 Cardiomyopathy, Familial Hypertrophic 55 0.055
82
BRT005 Barth Syndrome 53 0.055
83
END030 End Stage Renal Failure 51 0.055
84
P JRV003 Jervell and Lange-Nielsen Syndrome 49 0.055
85
P HYP076 Hyperthyroidism 48 0.055
86
NRM005 Neuromuscular Disease 45 0.055
87
INT007 Intermediate Coronary Syndrome 45 0.055
88
P MSC003 Muscular Atrophy 45 0.055
89
CSY001 C Syndrome 44 0.055
90
c FML191 Familial Long Qt Syndrome 40 0.055
91
c SHR030 Short Qt Syndrome 39 0.055
92
CRD137 Cardiogenic Shock 39 0.055
93
HYP017 Hypophosphatemia 39 0.055
94
PRP009 Peripartum Cardiomyopathy 38 0.055
95
P MSC033 Muscle Disorders 38 0.055
96
CRB009 Cerebritis 37 0.055
97
c LNG092 Long Qt Syndrome-3 36 0.055
98
c LNG053 Long Qt Syndrome 9 30 0.055
99
HSB001 His Bundle Tachycardia 18 0.055
100
P PRM002 Primary Hyperoxaluria 64 0.048
101
CST001 Costello Syndrome 64 0.048
102
c CHR089 Chronic Kidney Failure 61 0.048
103
P SDD001 Sudden Infant Death Syndrome 59 0.048
104
P OCL013 Oculodentodigital Dysplasia 57 0.048
105
P KDN018 Kidney Disease 57 0.048
106
P EMR001 Emery-Dreifuss Muscular Dystrophy 56 0.048
107
CHG001 Chagas Disease 53 0.048
108
P NRV007 Nervous System Disease 49 0.048
109
P TMT001 Timothy Syndrome 48 0.048
110
SLP005 Sleep Disorder 47 0.048
111
c LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 46 0.048
112
P PLY041 Polymyositis 45 0.048
113
CRN041 Carnitine-Acylcarnitine Translocase Deficiency 43 0.048
114
ART017 Aortic Disease 42 0.048
115
c FML058 Familial Dilated Cardiomyopathy 41 0.048
116
PRC012 Pericardial Effusion 41 0.048
117
c LNG047 Long Qt Syndrome 2 39 0.048
118
P THY054 Thyrotoxic Periodic Paralysis 39 0.048
119
P SPS003 Spastic Diplegia 37 0.048
120
c ACT076 Acute Myocarditis 36 0.048
121
ATN005 Autonomic Dysfunction 36 0.048
122
RGH001 Right Bundle Branch Block 35 0.048
123
c VNT013 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1 35 0.048
124
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 32 0.048
125
STR037 Stress Cardiomyopathy 32 0.048
126
c CRD093 Cardiomyopathy, Dilated, 1a 31 0.048
127
HRT008 Heart Conduction Disease 31 0.048
128
INF013 Inferior Myocardial Infarction 31 0.048
129
c LNG050 Long Qt Syndrome 5 30 0.048
130
GNT019 Giant Cell Myocarditis 28 0.048
131
c PRG106 Progressive Muscular Dystrophy 28 0.048
132
SPN148 Spondylometaphyseal Dysplasia Sedaghatian Type 28 0.048
133
c LNG051 Long Qt Syndrome 6 27 0.048
134
PRM025 Primary Bacterial Infectious Disease 27 0.048
135
ATN002 Autonomic Nervous System Disease 27 0.048
136
c LNG057 Long Qt Syndrome 13 24 0.048
137
MSC004 Muscle Tissue Disease 23 0.048
138
c LNG056 Long Qt Syndrome 12 22 0.048
139
P HRT017 Heart Tumor 21 0.048
140
c LNG093 Long Qt Syndrome-11 20 0.048
141
c AMY091 Amyotrophic Lateral Sclerosis 1 83 0.039
142
P PLM037 Pulmonary Hypertension 78 0.039
143
P HMC003 Hemochromatosis 75 0.039
144
c HYP595 Hypertension, Essential 68 0.039
145
VNH007 Von Hippel-Lindau Syndrome 68 0.039
146
P FML161 Familial Mediterranean Fever, Ar 67 0.039
147
BCK001 Becker Muscular Dystrophy 66 0.039
148
P DMN001 Diamond-Blackfan Anemia 66 0.039
149
P ANG001 Angelman Syndrome 66 0.039
150
P TBR001 Tuberous Sclerosis 65 0.039
151
P DRV001 Dravet Syndrome 65 0.039
152
P HLP001 Holoprosencephaly 62 0.039
153
PRP083 Porphyria, Acute Intermittent 62 0.039
154
KWS002 Kawasaki Disease 62 0.039
155
c SYS005 Systemic Scleroderma 62 0.039
156
c MLT024 Multiple Endocrine Neoplasia Iia 61 0.039
157
ACR007 Acromegaly 61 0.039
158
SKN016 Skin Disease 61 0.039
159
WGN006 Wegener Granulomatosis 59 0.039
160
P RSP003 Respiratory Failure 58 0.039
161
P SPN046 Spinal Muscular Atrophy 58 0.039
162
CRB039 Cerebrovascular Disease 58 0.039
163
PRP084 Propionicacidemia 57 0.039
164
P DRM010 Dermatomyositis 57 0.039
165
ANX002 Anxiety Disorder 57 0.039
166
LYM017 Lyme Disease 56 0.039
167
SPN186 Spinal Cord Injury 55 0.039
168
P LDD002 Liddle Syndrome 54 0.039
169
P EPL002 Epilepsy Syndrome 54 0.039
170
HMR004 Hemorrhagic Fever with Renal Syndrome 53 0.039
171
LGN002 Legionellosis 53 0.039
172
P STC001 Stickler Syndrome 52 0.039
173
c DYS166 Dysautonomia, Familial 52 0.039
174
RLP001 Relapsing Polychondritis 52 0.039
175
c CNT035 Central Nervous System Disease 52 0.039
176
CHL071 Child Syndrome 51 0.039
177
BTL001 Botulism 50 0.039
178
ATH003 Atherosclerosis 50 0.039
179
c MSC124 Muscular Dystrophy, Congenital 50 0.039
180
c PRX045 Peroxisome Biogenesis Disorder 1b 50 0.039
181
HYP056 Hypoglycemia 49 0.039
182
SNS001 Sensorineural Hearing Loss 49 0.039
183
MCR088 Microscopic Polyangiitis 49 0.039
184
P HYP192 Hypocalcemia, Autosomal Dominant 49 0.039
185
P PLY017 Polyarteritis Nodosa 49 0.039
186
P SZR006 Seizure Disorder 48 0.039
187
PTN001 Patent Foramen Ovale 48 0.039
188
CHL028 Childhood Type Dermatomyositis 48 0.039
189
c SCN006 Secondary Syphilis 48 0.039
190
WLL006 Wells Syndrome 48 0.039
191
THR013 Thoracic Outlet Syndrome 47 0.039
192
THR100 Thrombocytopenic Purpura, Autoimmune 47 0.039
193
c EHL055 Ehlers-Danlos Syndrome, Type Iii 47 0.039
194
FCL014 Focal Epilepsy 47 0.039
195
P PLY019 Polyneuropathy 46 0.039
196
OBS006 Obstructive Lung Disease 45 0.039
197
P FNC044 Fanconi Anemia, Complementation Group C 44 0.039
198
KDS001 Kid Syndrome 44 0.039
199
MTR046 Maternally Inherited Diabetes and Deafness 43 0.039
200
SPR099 Supravalvar Aortic Stenosis 43 0.039
201
c PND001 Pain Disorder 43 0.039
202
P TRC086 Trichohepatoenteric Syndrome 1 42 0.039
203
ADT003 Auditory System Disease 42 0.039
204
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 41 0.039
205
DXT001 Dextrocardia 41 0.039
206
P CNG018 Congenital Heart Block 41 0.039
207
LYM029 Lymphedema-Distichiasis Syndrome 41 0.039
208
P KLF001 Kleefstra Syndrome 41 0.039
209
HYP037 Hyperhomocysteinemia 40 0.039
210
CPT003 Cpt Deficiency, Hepatic, Type Ia 40 0.039
211
c BRG005 Brugada Syndrome 1 39 0.039
212
MNT002 Mental Depression 39 0.039
213
HTR003 Heterotaxy 38 0.039
214
NNN026 Noonan Syndrome with Multiple Lentigines 38 0.039
215
P HYP599 Hypoparathyroidism, Familial Isolated 38 0.039
216
P SPL050 Split Hand-Split Foot Malformation 38 0.039
217
CCN002 Cocaine Abuse 38 0.039
218
SCH068 Schwartz-Jampel Syndrome, Type 1 38 0.039
219
GDS001 Good Syndrome 37 0.039
220
c SMP007 Simpson-Golabi-Behmel Syndrome, Type 1 37 0.039
221
RSP006 Respiratory System Disease 36 0.039
222
NTR041 N-Terminal Acetyltransferase Deficiency 36 0.039
223
RGH009 Right Atrial Isomerism 36 0.039
224
P NRL007 Neurologic Diseases 35 0.039
225
P SPL037 Split Hand Foot Malformation 35 0.039
226
ALC010 Alcoholic Cardiomyopathy 35 0.039
227
c MYP072 Myopathy, Myofibrillar, 1 35 0.039
228
MYC005 Myocardial Stunning 35 0.039
229
c CNT015 Central Sleep Apnea 34 0.039
230
HRT007 Heart Cancer 34 0.039
231
CRN055 Carney Triad 34 0.039
232
PHC013 Phaeochromocytoma 34 0.039
233
CRB004 Cerebral Artery Occlusion 33 0.039
234
c FML250 Familial Progressive Cardiac Conduction Defect 33 0.039
235
MGL023 Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome, Somatic 33 0.039
236
ARR038 Arrhythmogenic Right Ventricular Dysplasia 11 33 0.039
237
ANG060 Angiopathy, Hereditary, with Nephropathy, Aneurysms, and Muscle Cramps 33 0.039
238
HTR014 Heterotaxy, Visceral, 1, X-Linked 32 0.039
239
c CTS034 Cutis Laxa, Autosomal Recessive Type 1 32 0.039
240
CPL011 Capillary Malformations, Congenital, 1, Somatic, Mosaic 32 0.039
241
GST007 Gastric Dilatation 31 0.039
242
EHL060 Ehlers-Danlos Syndrome Due to Tenascin X Deficiency 31 0.039
243
c VNT028 Ventricular Septal Defect 1 30 0.039
244
SBV001 Subvalvular Aortic Stenosis 30 0.039
245
PCW002 Pcwh Syndrome 30 0.039
246
PTN008 Patent Arterial Duct 29 0.039
247
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 29 0.039
248
P PLM040 Pulmonary Valve Disease 28 0.039
249
NSD001 Nose Disease 28 0.039
250
MTC028 Mitochondrial Cardiomyopathy 28 0.039
251
MYT003 Myotonic Disease 27 0.039
252
INT084 Intrinsic Cardiomyopathy 27 0.039
253
ARR030 Arrhythmogenic Right Ventricular Dysplasia 2 27 0.039
254
ARR035 Arrhythmogenic Right Ventricular Dysplasia 9 26 0.039
255
c CRD107 Cardiomyopathy, Dilated, 1r 26 0.039
256
MCL055 Mcleod Syndrome with or Without Chronic Granulomatous Disease 26 0.039
257
CRD201 Cardiomyopathy, Dilated, 1c, with or Without Lvnc 26 0.039
258
ARR029 Arrhythmogenic Right Ventricular Dysplasia 8 26 0.039
259
ARR040 Arrhythmogenic Right Ventricular Dysplasia 10 26 0.039
260
SPC003 Specific Developmental Disorder 25 0.039
261
MTC068 Mitochondrial Complex V Deficiency, Nuclear Type 2 25 0.039
262
ARR025 Arrhythmogenic Right Ventricular Dysplasia 5 25 0.039
263
c BRG003 Brugada Syndrome 3 24 0.039
264
SNT005 Sinoatrial Node Disease 24 0.039
265
ARR026 Arrhythmogenic Right Ventricular Dysplasia 1 24 0.039
266
c CRD104 Cardiomyopathy, Dilated, 1p 24 0.039
267
c GLY009 Glycogen Storage Disease Xv 23 0.039
268
SCN049 Second-Degree Atrioventricular Block 23 0.039
269
c LFT017 Left Ventricular Noncompaction 8 23 0.039
270
c VNT024 Ventricular Septal Defect 3 22 0.039
271
SHP003 Shapiro Syndrome 20 0.039
272
DFN007 Deafness Enamel Hypoplasia Nail Defects 20 0.039
273
MXD035 Mixed-Type Autoimmune Hemolytic Anemia 20 0.039
274
c VNT026 Ventricular Septal Defect 2 19 0.039
275
ATM069 Autoimmune Hemolytic Anemia, Warm Type 18 0.039
276
DRG014 Drug-Induced Autoimmune Hemolytic Anemia 18 0.039
277
ARR041 Arrhythmogenic Right Ventricular Dysplasia, Familial, 13 18 0.039
278
TBT001 Tabatznik Syndrome 18 0.039
279
TRT006 Torticollis Keloids Cryptorchidism Renal Dysplasia 18 0.039
280
c CRD173 Cardiomyopathy, Dilated, 1nn 18 0.039
281
CRD023 Cardiomyopathy Cataract Hip Spine Disease 17 0.039
282
P PHC014 Phocomelia 17 0.039
283
NTH002 Nathalie Syndrome 17 0.039
284
CNT017 Central Nervous System Origin Vertigo 17 0.039
285
KNS002 Kniest Like Dysplasia Lethal 16 0.039
286
19P001 19p13.12 Microdeletion Syndrome 16 0.039
287
CPT005 Cpt Ii Deficiency, Lethal Neonatal 16 0.039
288
WLL009 Woolly Hair Hypotrichosis Everted Lower Lip and Outstanding Ears 15 0.039
289
ATR074 Atrial Standstill 2 15 0.039
290
VNT005 Ventricular Extrasystoles with Syncopal Episodes - Perodactyly - Robin Sequence 14 0.039
291
PLY106 Polyneuropathy - Intellectual Disability - Acromicria - Premature Menopause 14 0.039
292
CNG288 Congenital Absence of Upper Arm and Forearm with Hand Present 13 0.039
293
HRS003 Hirschsprung Disease Ganglioneuroblastoma 12 0.039
294
MSC030 Muscular Fibrosis Multifocal Obstructed Vessels 12 0.039
295
c CRN176 Coronary Heart Disease 9 9 0.039
296
c ADL079 Adult Heart Tumor 7 0.039
297
ATR076 Atrophic Muscular Disease 5 0.039
298
HPT023 Hepatocellular Carcinoma 90 0.028
299
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 84 0.028
300
P DBT085 Diabetes Mellitus, Insulin-Dependent 82 0.028
301
CRH001 Crohn's Disease 80 0.028
302
P AST005 Asthma 77 0.028
303
ULC004 Ulcerative Colitis 75 0.028
304
MRF001 Marfan Syndrome 72 0.028
305
ANR002 Aniridia 72 0.028
306
CDS001 Cadasil 70 0.028
307
P WSK001 Wiskott-Aldrich Syndrome 68 0.028
308
P RBN001 Rubinstein-Taybi Syndrome 66 0.028
309
P BPL003 Bipolar Disorder 63 0.028
310
P HRM001 Hermansky-Pudlak Syndrome 62 0.028
311
PCK002 Pick Disease 61 0.028
312
WRN001 Werner Syndrome 61 0.028
313
c GLY008 Glycogen Storage Disease Ii 61 0.028
314
P KDN017 Kidney Cancer 60 0.028
315
P AMY004 Amyloidosis 60 0.028
316
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 60 0.028
317
c PNC108 Pancreatitis, Hereditary 59 0.028
318
TYP007 Typhoid Fever 59 0.028
319
LVR012 Liver Cirrhosis 59 0.028
320
P HMP002 Hemophagocytic Lymphohistiocytosis 59 0.028
321
P HYP055 Hypoplastic Left Heart Syndrome 58 0.028
322
LBR002 Leber Hereditary Optic Neuropathy 58 0.028
323
P HLT001 Holt-Oram Syndrome 58 0.028
324
c CNG006 Congenital Hypothyroidism 57 0.028
325
P ASP006 Aspergillosis 56 0.028
326
c PRM005 Primary Hyperparathyroidism 56 0.028
327
IMG001 Image Syndrome 56 0.028
328
c ATM010 Autoimmune Hemolytic Anemia 56 0.028
329
P RCK004 Rickets 55 0.028
330
CNT097 Central Hypoventilation Syndrome, Congenital 55 0.028
331
c MCL062 Mucolipidosis Ii Alpha/beta 55 0.028
332
RBR001 Roberts Syndrome 54 0.028
333
P SJG001 Sjogren's Syndrome 54 0.028
334
c MYT020 Myotonic Dystrophy 2 54 0.028
335
CRT002 Cartilage-Hair Hypoplasia 53 0.028
336
P ACR001 Aicardi-Goutieres Syndrome 53 0.028
337
RHM001 Rheumatic Fever 53 0.028
338
ACN002 Acanthosis Nigricans 53 0.028
339
KRN002 Kearns-Sayre Syndrome 53 0.028
340
P TMP003 Temporal Arteritis 53 0.028
341
P MLS001 Melas Syndrome 53 0.028
342
P MYP101 Myopathy, Centronuclear 53 0.028
343
P HYP086 Hypothyroidism 52 0.028
344
P MTH008 Methylmalonic Acidemia 52 0.028
345
P LMB006 Limb-Girdle Muscular Dystrophy 52 0.028
346
c LCL006 Localized Scleroderma 52 0.028
347
P ALP009 Alopecia Areata 52 0.028
348
YLL002 Yellow Fever 52 0.028
349
P HYP004 Hypercalcemia 52 0.028
350
HNT002 Hantavirus Pulmonary Syndrome 52 0.028
351
c MTB001 Metabolic Syndrome X 52 0.028
352
P SMP003 Simpson-Golabi-Behmel Syndrome 51 0.028
353
P GT001 Gout 51 0.028
354
P CHL002 Childhood Absence Epilepsy 51 0.028
355
CRN183 Carnitine Palmitoyltransferase Ii Deficiency 51 0.028
356
P MNN013 Meningitis 51 0.028
357
P CMP010 Complex Regional Pain Syndrome 51 0.028
358
P HYP069 Hyperparathyroidism 50 0.028
359
PRN023 Prion Disease 50 0.028
360
ULN003 Ulnar-Mammary Syndrome 49 0.028
361
CNN005 Connective Tissue Disease 49 0.028
362
ATX019 Ataxia with Vitamin E Deficiency 49 0.028
363
KRT002 Keratomalacia 49 0.028
364
P BRT004 Bartter Disease 48 0.028
365
NRT001 Neurotic Disorder 48 0.028
366
GTR002 Goiter 47 0.028
367
LRN003 Learning Disability 47 0.028
368
TNS005 Tonsillitis 47 0.028
369
P ECL001 Eclampsia 47 0.028
370
CGN006 Cogan Syndrome 46 0.028
371
OBS061 Obstructive Sleep Apnea 46 0.028
372
GST037 Gastroparesis 46 0.028
373
EVN001 Evans' Syndrome 46 0.028
374
DNN001 Danon Disease 46 0.028
375
IMP005 Impotence 46 0.028
376
SPN020 Spondylosis 46 0.028
377
MYC002 Mycobacterium Avium Complex Disease 46 0.028
378
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 46 0.028
379
P MTR012 Mitral Valve Disease 46 0.028
380
MTN003 Motion Sickness 45 0.028
381
CND002 Conduct Disorder 45 0.028
382
c ACT071 Acute Kidney Failure 45 0.028
383
c CNT033 Central Nervous System Cancer 45 0.028
384
NWC001 Newcastle Disease 45 0.028
385
P DRR001 Diarrhea 45 0.028
386
CHL068 Cholestasis 45 0.028
387
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 45 0.028
388
P LPD010 Lipodystrophy 45 0.028
389
TRY001 Trypanosomiasis 45 0.028
390
NXS001 Naxos Disease 44 0.028
391
STT002 Status Asthmaticus 44 0.028
392
CLS010 Cluster Headache 44 0.028
393
P SYP003 Syphilis 44 0.028
394
END021 Endomyocardial Fibrosis 44 0.028
395
c CCK005 Cockayne Syndrome, Type a 43 0.028
396
P CLL015 Collagen Disease 43 0.028
397
BRN106 Burns 43 0.028
398
P END033 Endocarditis 43 0.028
399
TRN015 Transient Cerebral Ischemia 43 0.028
400
END020 Endocardial Fibroelastosis 43 0.028
401
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 43 0.028
402
GRN039 Greenberg Skeletal Dysplasia 43 0.028
403
c ART115 Aortic Valve Disease 1 43 0.028
404
ADL002 Adult Syndrome 43 0.028
405
P MYF003 Myofibrillar Myopathy 43 0.028
406
HYP266 Hypoxia 42 0.028
407
CRN017 Coronary Thrombosis 42 0.028
408
P PSD015 Pseudohypoparathyroidism 42 0.028
409
P CRV039 Cervicitis 42 0.028
410
ADN002 Adenoiditis 42 0.028
411
INF034 Infective Endocarditis 42 0.028
412
EBS001 Ebstein Anomaly 42 0.028
413
P ENC018 Encephalopathy 42 0.028
414
P HYP366 Hyperkalemic Periodic Paralysis, Type 2 42 0.028
415
P PHS004 Phosphoribosylpyrophosphate Synthetase Superactivity 42 0.028
416
ACT098 Acute Erythroid Leukemia 41 0.028
417
P EXN002 Exanthem 41 0.028
418
PRP007 Priapism 41 0.028
419
DRG003 Drug Dependence 41 0.028
420
P MSC007 Muscle Hypertrophy 41 0.028
421
c INV001 Invasive Aspergillosis 40 0.028
422
PRN037 Prinzmetal's Variant Angina 40 0.028
423
AGR002 Agoraphobia 40 0.028
424
P PSD003 Pseudohypoaldosteronism 40 0.028
425
MCR103 Microtia 40 0.028
426
c CMP058 Complex Regional Pain Syndrome Type 1 40 0.028
427
NRN002 Neuronitis 40 0.028
428
P PLM041 Pulmonary Valve Stenosis 40 0.028
429
DDN006 Duodenitis 40 0.028
430
AGG002 Aggressive Systemic Mastocytosis 39 0.028
431
c CCK006 Cockayne Syndrome, Type B 39 0.028
432
MLF002 Malouf Syndrome 39 0.028
433
END072 Endotheliitis 39 0.028
434
TRN012 Transient Global Amnesia 39 0.028
435
CRD001 Cardiac Tamponade 39 0.028
436
ART004 Aortic Atherosclerosis 39 0.028
437
GRW007 Growth Hormone Deficiency 38 0.028
438
ESN011 Eisenmenger Syndrome 38 0.028
439
c MLG132 Malignant Hyperthermia Susceptibility 1 38 0.028
440
c HRT021 Heart Block, Progressive, Type Ia 38 0.028
441
c EMR011 Emery-Dreifuss Muscular Dystrophy 2, Ad 38 0.028
442
ANH002 Anhidrosis 38 0.028
443
P RST002 Restrictive Cardiomyopathy 38 0.028
444
CNV002 Conversion Disorder 37 0.028
445
c DYS156 Dyserythropoietic Anemia, Congenital, Type Ia 37 0.028
446
PNN001 Panniculitis 37 0.028
447
MYT022 Myotubular Myopathy, X-Linked 37 0.028
448
BRN080 Brain Ischemia 37 0.028
449
MYF002 Myofascial Pain Syndrome 36 0.028
450
P DYS021 Dysautonomia 36 0.028
451
VSC047 Vascular Malformation 35 0.028
452
PRT030 Parathyroid Gland Disease 35 0.028
453
THY030 Thyroid Gland Disease 35 0.028
454
NSY001 N Syndrome 34 0.028
455
PRP021 Peripheral Nervous System Neoplasm 34 0.028
456
SKN005 Skin Atrophy 34 0.028
457
c ATM022 Autoimmune Myocarditis 34 0.028
458
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 34 0.028
459
CRB008 Cerebral Atherosclerosis 33 0.028
460
c CNG012 Congenital Generalized Lipodystrophy 33 0.028
461
HYP022 Hypohidrosis 33 0.028
462
URN009 Urinary System Disease 33 0.028
463
FDB001 Foodborne Botulism 33 0.028
464
PHY002 Physical Disorder 33 0.028
465
FTT003 Fatty Acid Oxidation Disorders 33 0.028
466
MNN032 Meningococcal Meningitis 33 0.028
467
PLM068 Pulmonary Vein Stenosis 33 0.028
468
GLS004 Glossopharyngeal Neuralgia 33 0.028
469
c SYS007 Systemic Capillary Leak Syndrome 33 0.028
470
c MSC112 Muscular Dystrophy, Limb-Girdle, Type 1b 32 0.028
471
c DYS170 Dyserythropoietic Anemia, Congenital, Type Ii 32 0.028
472
ATX003 Ataxia with Isolated Vitamin E Deficiency 32 0.028
473
CTS011 Cutis Marmorata Telangiectatica Congenita 32 0.028
474
INT088 Intrinsic Factor Deficiency 32 0.028
475
LWN001 Lown-Ganong-Levine Syndrome 32 0.028
476
c HMC021 Hemochromatosis, Type 2a 32 0.028
477
MDY003 Mody, Type Ii 32 0.028
478
PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 32 0.028
479
c LNG096 Long Qt Syndrome 15 32 0.028
480
WDH003 Woodhouse-Sakati Syndrome 31 0.028
481
TRC062 Tricuspid Atresia 31 0.028
482
SPC010 Speech and Communication Disorders 31 0.028
483
P ATX010 Ataxia Neuropathy Spectrum 31 0.028
484
DXR001 Doxorubicin Induced Cardiomyopathy 30 0.028
485
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 30 0.028
486
c MYP011 Myopathy Congenital 30 0.028
487
ADJ001 Adjustment Disorder 30 0.028
488
ADR009 Adrenal Cortex Disease 30 0.028
489
c EMR017 Emery-Dreifuss Muscular Dystrophy 1, X-Linked 30 0.028
490
c LNG098 Long Qt Syndrome 14 30 0.028
491
DPH006 Diaphragmatic Eventration 30 0.028
492
c CHR096 Chronic Pulmonary Heart Disease 30 0.028
493
SXL003 Sexual Disorder 30 0.028
494
FCT008 Factitious Disorder 30 0.028
495
c CRD082 Cardiomyopathy, Dilated, 1gg 30 0.028
496
FRY001 Frey Syndrome 29 0.028
497
SCP009 Scapuloperoneal Myopathy, X-Linked Dominant 29 0.028
498
IVC001 Ivic Syndrome 29 0.028
499
HYP540 Hypertension, Diastolic 29 0.028
500
c BRG006 Brugada Syndrome 2 29 0.028
501
GND003 Gonadal Disease 28 0.028
502
CLC007 Calcium Metabolism Disease 28 0.028
503
c ALP005 Alpha Chain Disease 28 0.028
504
CHR543 Chromosome 2q37 Deletion Syndrome 28 0.028
505
c CNG031 Congenital Nervous System Abnormality 28 0.028
506
ATN003 Autonomic Nervous System Neoplasm 28 0.028
507
SBN001 Subendocardial Myocardial Infarction 28 0.028
508
ATR060 Atrial Standstill, Digenic 27 0.028
509
c CRD155 Cardiomyopathy, Dilated, 1kk 27 0.028
510
c CRD199 Cardiomyopathy, Hypertrophic 6 27 0.028
511
WTH001 Withdrawal Disorder 27 0.028
512
CNG134 Congenitally Corrected Transposition of the Great Arteries 27 0.028
513
c CRD091 Cardiomyopathy, Dilated, 1dd 27 0.028
514
c CRD097 Cardiomyopathy, Dilated, 1d 27 0.028
515
MYP056 Myopathy, X-Linked, with Postural Muscle Atrophy 26 0.028
516
BRN055 Bronchogenic Cyst 26 0.028
517
c CRD114 Cardiomyopathy, Dilated, 1m 26 0.028
518
VNT011 Ventricular Fibrillation, Familial, 1 26 0.028
519
INF133 Inferior Vena Cava Interruption 26 0.028
520
LNS003 Lens Disease 26 0.028
521
c LNG094 Long Qt Syndrome-10 26 0.028
522
DMD003 Dmd-Associated Dilated Cardiomyopathy 26 0.028
523
c CRD149 Cardiomyopathy, Dilated, 1jj 26 0.028
524
RDN001 Reading Disorder 25 0.028
525
P EMR004 Emery-Dreifuss Muscular Dystrophy, X-Linked 25 0.028
526
c FML272 Familial Sick Sinus Syndrome 25 0.028
527
THR099 Third-Degree Atrioventricular Block 25 0.028
528
HMN017 Hemangioma Thrombocytopenia Syndrome 25 0.028
529
c CRD206 Cardiomyopathy, Hypertrophic, 11 25 0.028
530
c CRD103 Cardiomyopathy, Dilated, 1t 25 0.028
531
TXC010 Toxic Myocarditis 25 0.028
532
c CRD101 Cardiomyopathy, Dilated, 1x 25 0.028
533
BLD054 Blood Protein Disease 24 0.028
534
GLY075 Glycogen Storage Disease Due to Acid Maltase Deficiency 24 0.028
535
c CRD063 Cardiomyopathy, Dilated, 2a 24 0.028
536
c LFT018 Left Ventricular Noncompaction 10 24 0.028
537
c CRD105 Cardiomyopathy, Dilated, 1o 24 0.028
538
c CRD187 Cardiomyopathy, Dilated, 3b 24 0.028
539
c CRD090 Cardiomyopathy, Dilated, 1l 24 0.028
540
MDY006 Mody, Type Iv 24 0.028
541
c BRG009 Brugada Syndrome 7 24 0.028
542
LFT013 Left Ventricular Noncompaction 1, with or Without Congenital Heart Defects 24 0.028
543
c CRD111 Cardiomyopathy, Dilated, 1i 23 0.028
544
IMP003 Impaired Renal Function Disease 23 0.028
545
c CRD080 Cardiomyopathy, Dilated, 1g 23 0.028
546
SDD002 Sudden Infant Death with Dysgenesis of the Testes Syndrome 23 0.028
547
c JRV002 Jervell and Lange-Nielsen Syndrome 2 23 0.028
548
c CNG420 Congenital Muscular Dystrophy Due to Lmna Mutation 23 0.028
549
c CRD102 Cardiomyopathy, Dilated, 1j 23 0.028
550
ARR037 Arrhythmogenic Right Ventricular Dysplasia 12 23 0.028
551
c ATR038 Atrial Fibrillation, Familial, 3 23 0.028
552
c CRD159 Cardiomyopathy, Dilated, 1hh 23 0.028
553
PST048 Postural Orthostatic Tachycardia Syndrome 23 0.028
554
INT010 Intracranial Embolism 23 0.028
555
c AST039 Asthma 2 23 0.028
556
CRD191 Cardiomyopathy, Dilated, 1aa, with or Without Lvnc 23 0.028
557
c CRD113 Cardiomyopathy, Dilated, 1v 23 0.028
558
CMB025 Combined Oxidative Phosphorylation Deficiency 10 22 0.028
559
c CRD153 Cardiomyopathy, Dilated, 2b 22 0.028
560
c CRD112 Cardiomyopathy, Dilated, 1u 22 0.028
561
c CRD108 Cardiomyopathy, Dilated, 1bb 22 0.028
562
c CRD092 Cardiomyopathy, Dilated, 1w 22 0.028
563
PGD001 Pagod Syndrome 22 0.028
564
MYP092 Myopathy, Early-Onset, with Fatal Cardiomyopathy 22 0.028
565
HRY002 Hairy Tongue 22 0.028
566
c CRD060 Cardiomyopathy, Dilated, 1z 22 0.028
567
P FML187 Familial Hypertension 21 0.028
568
c DYS145 Dystonia 23 21 0.028
569
MTC088 Mitochondrial Dna Depletion Syndrome 13 21 0.028
570
c CRD096 Cardiomyopathy, Dilated, 1ee 21 0.028
571
c CRD162 Cardiomyopathy, Dilated, 1ii 21 0.028
572
c CRD115 Cardiomyopathy, Dilated, 1cc 21 0.028
573
c CRD064 Cardiomyopathy, Dilated, 1ff 21 0.028
574
MND006 Mondor Disease 21 0.028
575
ANT054 Anotia 21 0.028
576
c BNG076 Benign Exophthalmos Syndrome 21 0.028
577
INT062 Interstitial Myocarditis 21 0.028
578
MTC078 Mitochondrial Dna Depletion Syndrome 11 20 0.028
579
CMB054 Combined Oxidative Phosphorylation Deficiency 23 20 0.028
580
CHR515 Chronic Atrial and Intestinal Dysrhythmia 20 0.028
581
c AST037 Asthma 1 20 0.028
582
P ACT080 Acute Pulmonary Heart Disease 20 0.028
583
c EMR015 Emery-Dreifuss Muscular Dystrophy 5, Autosomal Dominant 20 0.028
584
c PLM121 Pulmonary Hypertension, Primary, 4 20 0.028
585
BRC019 Brachycephalofrontonasal Dysplasia 20 0.028
586
BSL014 Basilar Migraine 19 0.028
587
c ATR068 Atrial Fibrillation, Familial, 14 19 0.028
588
c BRG004 Brugada Syndrome 4 19 0.028
589
c EMR012 Emery-Dreifuss Muscular Dystrophy 3, Ar 19 0.028
590
AND005 Androgen Insensitivity Syndrome, Mild 19 0.028
591
CRB031 Cerebral Arterial Disease 19 0.028
592
BRM003 Biermer's Disease 18 0.028
593
VNT009 Ventricular Tachycardia, Idiopathic 18 0.028
594
HCS001 Hec Syndrome 18 0.028
595
c EMR003 Emery-Dreifuss Muscular Dystrophy, Dominant Type 17 0.028
596
c CNG404 Congenital Heart Defects, Multiple Types, 4 17 0.028
597
c SCK022 Sick Sinus Syndrome 3 16 0.028
598
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 16 0.028
599
APN006 Apnea of Prematurity 16 0.028
600
NSP003 Nasopharyngeal Disease 16 0.028
601
TMM012 Tmem70-Related Mitochondrial Encephalo-Cardio-Myopathy 16 0.028
602
IDP076 Idiopathic Ventricular Fibrillation, Not Brugada Type 15 0.028
603
c SCN015 Scn1a-Related Severe Myoclonic Epilepsy in Infancy 15 0.028
604
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 15 0.028
605
20P001 20p12.3 Microdeletion Syndrome 15 0.028
606
CRN253 Carnitine Palmitoyl Transferase Ii Deficiency, Neonatal Form 15 0.028
607
THL007 Thalamic Degeneration Symmetrical Infantile 14 0.028
608
MCH010 Michels Syndrome 14 0.028
609
RBB001 Ribbing Disease 14 0.028
610
CRB087 Cerebral Arteriosclerosis 14 0.028
611
CPT004 Cpt Deficiency, Hepatic, Type Ii 14 0.028
612
EYC003 Eye Accommodation Disease 14 0.028
613
CRN252 Carnitine Palmitoyl Transferase Ii Deficiency, Severe Infantile Form 14 0.028
614
c VNT012 Ventricular Fibrillation, Paroxysmal Familial, 2 13 0.028
615
16P006 16p11.2p12.2 Microdeletion Syndrome 13 0.028
616
PLY088 Polyvalvular Heart Disease Syndrome 13 0.028
617
BRC025 Brachydactyly Long Thumb Type 13 0.028
618
DGT004 Digitalis Poisoning 13 0.028
619
SBR006 Subaortic Stenosis Short Stature Syndrome 13 0.028
620
PLM008 Pulmonary Subvalvular Stenosis 12 0.028
621
EXT038 Extrasystoles Short Stature Hyperpigmentation Microcephaly 12 0.028
622
ECT023 Ectodermal Dysplasia, Hidrotic, Christianson-Fourie Type 12 0.028
623
c FML196 Familial Isolated Hypoparathyroidism Due to Agenesis of Parathyroid Gland 12 0.028
624
c ATR025 Atrial Fibrillation, Familial, 2 12 0.028
625
BDR001 Bidirectional Tachycardia 11 0.028
626
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 11 0.028
627
ANR042 Aniridia - Ptosis - Intellectual Disability - Familial Obesity 10 0.028
628
HYP611 Hypoparathyroidism, X-Linked 10 0.028
629
CRN208 Coronary Sinus Atresia 9 0.028
630
VSC009 Vascular Skin Disease 9 0.028
631
ARR008 Arrhythmogenic Right Ventricular Dysplasia/cardiomyopathy 5 8 0.028
632
ARR011 Arrhythmogenic Right Ventricular Dysplasia/cardiomyopathy 8 7 0.028
633
FCT015 Factor 2 Deficiency 7 0.028
634
HRT029 Heart Tumor of the Child 7 0.028
635
c RNL016 Renal Infectious Disease 7 0.028
636
PLM060 Pulmonary Branches Stenosis 6 0.028
637
ARR006 Arrhythmogenic Right Ventricular Dysplasia/cardiomyopathy 3 5 0.028
638
INT074 Intracranial Arteriosclerosis 3 0.028
639
ART033 Aortic Valves Stenosis of the Child 2 0.028