Search results for "arrhythmia"

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

664 hits were found for 'arrhythmia'

# Family MCID Name MIFTS Score
1
CRD054 Cardiac Arrhythmia, Ankyrin-B-Related 23 3.763
2
PHC009 Phocomelia Ectrodactyly Deafness Sinus Arrhythmia 6 3.119
3
PHC016 Phocomelia-Ectrodactyly, Ear Malformation, Deafness, and Sinus Arrhythmia 15 3.110
4
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 2.714
5
WLF001 Wolff-Parkinson-White Syndrome 58 2.279
6
SNT004 Sinoatrial Node Dysfunction and Deafness 25 2.264
7
SDD004 Sudden Arrhythmia Death Syndrome 13 2.264
8
c CRD099 Cardiomyopathy, Dilated, 1e 42 2.178
9
NTR041 N-Terminal Acetyltransferase Deficiency 34 2.161
10
P CRD011 Cardiomyopathy 66 0.222
11
P ATR011 Atrial Fibrillation 63 0.218
12
P MYC007 Myocardial Infarction 80 0.201
13
c CNG401 Congenital Heart Disease 67 0.190
14
c FML001 Familial Atrial Fibrillation 59 0.188
15
P LNG028 Long Qt Syndrome 67 0.178
16
SDD007 Sudden Cardiac Death 46 0.178
17
c VNT013 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1 46 0.167
18
c CRN175 Coronary Heart Disease 4 19 0.167
19
P HRT032 Heart Disease 64 0.163
20
c CRN172 Coronary Heart Disease 3 19 0.156
21
P CRD132 Cardiac Conduction Defect 35 0.153
22
c CLD010 Cold-Induced Sweating Syndrome 1 43 0.148
23
VNT011 Ventricular Fibrillation, Familial, 1 35 0.148
24
CRD119 Cardiac Arrest 63 0.146
25
SYN036 Syncope 45 0.146
26
c ACT075 Acute Myocardial Infarction 61 0.135
27
CNG034 Congestive Heart Failure 72 0.133
28
P BRG001 Brugada Syndrome 59 0.133
29
c DLT002 Dilated Cardiomyopathy 75 0.130
30
c CRN174 Coronary Heart Disease 2 19 0.130
31
SNG003 Single Ventricular Heart 23 0.130
32
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 56 0.127
33
ATR060 Atrial Standstill, Digenic 51 0.127
34
P CRN178 Coronary Heart Disease 6 22 0.124
35
P CRN211 Coronary Artery Disease 74 0.121
36
ISC004 Ischemia 56 0.121
37
P SCK002 Sick Sinus Syndrome 49 0.118
38
P HYP061 Hypertrophic Cardiomyopathy 64 0.112
39
P PRX010 Paroxysmal Ventricular Fibrillation 33 0.108
40
CRD003 Cardiac Sarcoidosis 39 0.108
41
ISC006 Ischemic Heart Disease 54 0.105
42
c CRN214 Coronary Heart Disease 5 22 0.101
43
P MYT002 Myotonic Dystrophy 46 0.098
44
HYP005 Hypokalemia 52 0.098
45
P MSC005 Muscular Dystrophy 64 0.094
46
FNT004 Fainting 33 0.094
47
ATR024 Atrial Fibrillation and Stroke 19 0.094
48
P MYC008 Myocarditis 56 0.090
49
PRP027 Peripheral Vascular Disease 69 0.086
50
PRN021 Paranasal Sinus Disease 50 0.086
51
NSL022 Nasal Cavity Disease 41 0.086
52
STR067 Stroke, Ischemic 74 0.081
53
ART111 Artery Disease 56 0.081
54
P AND016 Andersen Syndrome 57 0.077
55
TTR001 Tetralogy of Fallot 69 0.077
56
ART021 Arteriosclerosis 59 0.077
57
ANR040 Aneurysm 56 0.077
58
SYS003 Systolic Heart Failure 42 0.077
59
P MYP004 Myopathy 67 0.072
60
P SLP006 Sleep Apnea 60 0.072
61
TRN044 Transposition of the Great Arteries 48 0.072
62
ATR057 Atrioventricular Block 49 0.072
63
HYP006 Hypertensive Heart Disease 49 0.072
64
HRT012 Heart Valve Disease 39 0.072
65
CRN030 Coronary Stenosis 50 0.072
66
c MYC058 Myocardial Infarction 2 28 0.072
67
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 55 0.066
68
SLP005 Sleep Disorder 52 0.066
69
VND001 Vein Disease 51 0.066
70
P EPL164 Epilepsy 60 0.066
71
P NRP001 Neuropathy 57 0.066
72
ATN004 Autonomic Neuropathy 44 0.066
73
ATR055 Atrial Septal Aneurysm 23 0.066
74
P RTT002 Rett Syndrome 77 0.061
75
c LNG044 Long Qt Syndrome 1 59 0.061
76
P KDN018 Kidney Disease 64 0.061
77
RSP006 Respiratory System Disease 61 0.061
78
VSC007 Vascular Disease 51 0.061
79
P LFT003 Left Ventricular Noncompaction 48 0.061
80
OBS061 Obstructive Sleep Apnea 61 0.061
81
SKN023 Skin Tag 48 0.061
82
P SPS003 Spastic Diplegia 49 0.061
83
c SHR030 Short Qt Syndrome 45 0.061
84
HSB001 His Bundle Tachycardia 21 0.061
85
c CRN173 Coronary Heart Disease 8 19 0.061
86
DBT002 Diabetic Autonomic Neuropathy 37 0.061
87
FBR012 Fabry Disease 68 0.054
88
BRT005 Barth Syndrome 53 0.054
89
P RFS001 Refsum Disease 60 0.054
90
DCH001 Duchenne Muscular Dystrophy 81 0.054
91
c MYT021 Myotonic Dystrophy 1 64 0.054
92
c LNG047 Long Qt Syndrome 2 42 0.054
93
c CRD194 Cardiomyopathy, Familial Hypertrophic 55 0.054
94
P TMT001 Timothy Syndrome 58 0.054
95
P SDD001 Sudden Infant Death Syndrome 60 0.054
96
CSY001 C Syndrome 49 0.054
97
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.054
98
c LNG051 Long Qt Syndrome 6 30 0.054
99
c CHR089 Chronic Kidney Failure 67 0.054
100
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 41 0.054
101
c LNG092 Long Qt Syndrome-3 36 0.054
102
INT007 Intermediate Coronary Syndrome 52 0.054
103
c LNG053 Long Qt Syndrome 9 34 0.054
104
HYP056 Hypoglycemia 60 0.054
105
P HYP076 Hyperthyroidism 59 0.054
106
NRM005 Neuromuscular Disease 56 0.054
107
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 28 0.054
108
P THY054 Thyrotoxic Periodic Paralysis 46 0.054
109
STR037 Stress Cardiomyopathy 37 0.054
110
c BRN108 Branchiootic Syndrome 1 36 0.054
111
END030 End Stage Renal Failure 53 0.054
112
P MSC003 Muscular Atrophy 51 0.054
113
P MSC033 Muscle Disorders 52 0.054
114
HYP017 Hypophosphatemia 43 0.054
115
RGH001 Right Bundle Branch Block 43 0.054
116
PRP009 Peripartum Cardiomyopathy 41 0.054
117
P SPL050 Split Hand-Split Foot Malformation 34 0.054
118
c FML191 Familial Long Qt Syndrome 39 0.054
119
CRD137 Cardiogenic Shock 44 0.054
120
CNG288 Congenital Absence of Upper Arm and Forearm with Hand Present 12 0.054
121
P PHC014 Phocomelia 18 0.054
122
CRB009 Cerebritis 36 0.054
123
c HYP595 Hypertension, Essential 69 0.047
124
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.047
125
CST001 Costello Syndrome 68 0.047
126
P JRV003 Jervell and Lange-Nielsen Syndrome 53 0.047
127
BCK001 Becker Muscular Dystrophy 68 0.047
128
c MSC124 Muscular Dystrophy, Congenital 57 0.047
129
ACR007 Acromegaly 66 0.047
130
c ART101 Aortic Valve Disease 2 56 0.047
131
P NRV007 Nervous System Disease 71 0.047
132
P URF003 Urofacial Syndrome 1 51 0.047
133
P OCL013 Oculodentodigital Dysplasia 58 0.047
134
P SYS005 Systemic Scleroderma 60 0.047
135
CRN041 Carnitine-Acylcarnitine Translocase Deficiency 42 0.047
136
c LNG050 Long Qt Syndrome 5 43 0.047
137
ACR041 Acromelic Frontonasal Dysostosis 45 0.047
138
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 59 0.047
139
CRB039 Cerebrovascular Disease 49 0.047
140
CPT005 Cpt Ii Deficiency, Lethal Neonatal 25 0.047
141
URN009 Urinary System Disease 52 0.047
142
P EMR001 Emery-Dreifuss Muscular Dystrophy 57 0.047
143
ATN002 Autonomic Nervous System Disease 46 0.047
144
ADR038 Adermatoglyphia 39 0.047
145
ARR030 Arrhythmogenic Right Ventricular Dysplasia 2 26 0.047
146
c LNG093 Long Qt Syndrome-11 20 0.047
147
c LNG056 Long Qt Syndrome 12 28 0.047
148
c LNG057 Long Qt Syndrome 13 26 0.047
149
CHG001 Chagas Disease 62 0.047
150
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 29 0.047
151
MTC068 Mitochondrial Complex V Deficiency, Nuclear Type 2 25 0.047
152
HRT008 Heart Conduction Disease 43 0.047
153
P MSC007 Muscle Hypertrophy 55 0.047
154
ADM013 Adamantinoma of Long Bones 57 0.047
155
ART017 Aortic Disease 57 0.047
156
c CRD093 Cardiomyopathy, Dilated, 1a 30 0.047
157
CNT017 Central Nervous System Origin Vertigo 27 0.047
158
ATN005 Autonomic Dysfunction 44 0.047
159
c CRN177 Coronary Heart Disease 7 21 0.047
160
PRC012 Pericardial Effusion 50 0.047
161
BRT030 Birth Defects 44 0.047
162
GNT019 Giant Cell Myocarditis 31 0.047
163
P PLY041 Polymyositis 49 0.047
164
P HRT017 Heart Tumor 34 0.047
165
c CRN176 Coronary Heart Disease 9 19 0.047
166
c ACT076 Acute Myocarditis 40 0.047
167
INF013 Inferior Myocardial Infarction 36 0.047
168
c PRG106 Progressive Muscular Dystrophy 40 0.047
169
IMP003 Impaired Renal Function Disease 36 0.047
170
PRM025 Primary Bacterial Infectious Disease 42 0.047
171
MSC004 Muscle Tissue Disease 35 0.047
172
PRP083 Porphyria, Acute Intermittent 54 0.038
173
SKN016 Skin Disease 69 0.038
174
c GLY008 Glycogen Storage Disease Ii 59 0.038
175
P FML161 Familial Mediterranean Fever, Ar 64 0.038
176
P LKM068 Leukemia, Chronic Myeloid, Somatic 65 0.038
177
PRP084 Propionicacidemia 59 0.038
178
P HMC003 Hemochromatosis 71 0.038
179
P RSP003 Respiratory Failure 68 0.038
180
CPT003 Cpt Deficiency, Hepatic, Type Ia 41 0.038
181
c SPN225 Spondyloarthropathy 1 62 0.038
182
VNH007 Von Hippel-Lindau Syndrome 69 0.038
183
c MLT024 Multiple Endocrine Neoplasia Iia 64 0.038
184
P NNN008 Noonan Syndrome 1 64 0.038
185
SCH068 Schwartz-Jampel Syndrome, Type 1 34 0.038
186
P PLM037 Pulmonary Hypertension 78 0.038
187
P SPN046 Spinal Muscular Atrophy 62 0.038
188
P SZR006 Seizure Disorder 56 0.038
189
PCK002 Pick Disease 66 0.038
190
SPR099 Supravalvar Aortic Stenosis 49 0.038
191
KWS002 Kawasaki Disease 70 0.038
192
c EHL055 Ehlers-Danlos Syndrome, Type Iii 49 0.038
193
P LDD002 Liddle Syndrome 54 0.038
194
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 56 0.038
195
c LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 41 0.038
196
P DMN001 Diamond-Blackfan Anemia 69 0.038
197
MGL023 Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome, Somatic 34 0.038
198
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.038
199
HTR014 Heterotaxy, Visceral, 1, X-Linked 31 0.038
200
WGN006 Wegener Granulomatosis 63 0.038
201
c MYP072 Myopathy, Myofibrillar, 1 39 0.038
202
P HYP192 Hypocalcemia, Autosomal Dominant 50 0.038
203
P HYP599 Hypoparathyroidism, Familial Isolated 35 0.038
204
ANG060 Angiopathy, Hereditary, with Nephropathy, Aneurysms, and Muscle Cramps 30 0.038
205
LYM029 Lymphedema-Distichiasis Syndrome 38 0.038
206
P BPL003 Bipolar Disorder 58 0.038
207
CHL071 Child Syndrome 58 0.038
208
PCW002 Pcwh Syndrome 28 0.038
209
P DRM010 Dermatomyositis 59 0.038
210
DBT090 Diabetes and Deafness, Maternally Inherited 32 0.038
211
CPT004 Cpt Deficiency, Hepatic, Type Ii 25 0.038
212
c PRX045 Peroxisome Biogenesis Disorder 1b 50 0.038
213
ARR038 Arrhythmogenic Right Ventricular Dysplasia 11 29 0.038
214
FCL014 Focal Epilepsy 55 0.038
215
ALL026 Allergic Hypersensitivity Disease 53 0.038
216
ARR026 Arrhythmogenic Right Ventricular Dysplasia 1 26 0.038
217
P MYL006 Myeloid Leukemia 67 0.038
218
CPL011 Capillary Malformations, Congenital, 1, Somatic, Mosaic 36 0.038
219
NNN026 Noonan Syndrome with Multiple Lentigines 48 0.038
220
c GLY009 Glycogen Storage Disease Xv 23 0.038
221
P HLP001 Holoprosencephaly 62 0.038
222
ARR035 Arrhythmogenic Right Ventricular Dysplasia 9 23 0.038
223
P MCR113 Microvascular Complications of Diabetes 3 48 0.038
224
HRT007 Heart Cancer 51 0.038
225
P STC001 Stickler Syndrome 53 0.038
226
c BRG005 Brugada Syndrome 1 42 0.038
227
ARR029 Arrhythmogenic Right Ventricular Dysplasia 8 22 0.038
228
KDS001 Kid Syndrome 53 0.038
229
ARR040 Arrhythmogenic Right Ventricular Dysplasia 10 25 0.038
230
c LFT017 Left Ventricular Noncompaction 8 22 0.038
231
c CRD199 Cardiomyopathy, Hypertrophic 6 29 0.038
232
ARR025 Arrhythmogenic Right Ventricular Dysplasia 5 24 0.038
233
c FML250 Familial Progressive Cardiac Conduction Defect 32 0.038
234
P MYF003 Myofibrillar Myopathy 39 0.038
235
ATH003 Atherosclerosis 63 0.038
236
LYM017 Lyme Disease 64 0.038
237
c BRG003 Brugada Syndrome 3 25 0.038
238
c CRD107 Cardiomyopathy, Dilated, 1r 21 0.038
239
CNV002 Conversion Disorder 45 0.038
240
P ENC018 Encephalopathy 59 0.038
241
LGN002 Legionellosis 61 0.038
242
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.038
243
NSD001 Nose Disease 51 0.038
244
c VNT024 Ventricular Septal Defect 3 25 0.038
245
ARR041 Arrhythmogenic Right Ventricular Dysplasia, Familial, 13 19 0.038
246
PTN001 Patent Foramen Ovale 55 0.038
247
BTL001 Botulism 52 0.038
248
CRD201 Cardiomyopathy, Dilated, 1c, with or Without Lvnc 22 0.038
249
LNG099 Lung Disease 63 0.038
250
ATX003 Ataxia with Isolated Vitamin E Deficiency 36 0.038
251
HTR003 Heterotaxy 41 0.038
252
c CRD173 Cardiomyopathy, Dilated, 1nn 20 0.038
253
HMR004 Hemorrhagic Fever with Renal Syndrome 52 0.038
254
c VNT028 Ventricular Septal Defect 1 30 0.038
255
c ATR074 Atrial Standstill 2 19 0.038
256
c LKM060 Leukemia, Acute Lymphoblastic 3 49 0.038
257
WLL006 Wells Syndrome 57 0.038
258
DBT084 Diabetes Mellitus, Ketosis-Prone 28 0.038
259
CND002 Conduct Disorder 54 0.038
260
c SMP007 Simpson-Golabi-Behmel Syndrome, Type 1 38 0.038
261
c CNT035 Central Nervous System Disease 60 0.038
262
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.038
263
P PLY019 Polyneuropathy 53 0.038
264
AYM001 Ayme-Gripp Syndrome 40 0.038
265
EHL060 Ehlers-Danlos Syndrome Due to Tenascin X Deficiency 29 0.038
266
c DBT040 Diabetes Mellitus, Insulin-Dependent, 2 26 0.038
267
RHM029 Rheumatic Fever-Related Antigen Rheumatic Fever, Acute, Susceptibility to, Included 24 0.038
268
CHR586 Chromosome 16p12.2-P11.2 Deletion Syndrome, 7.1- to 8.7-Mb 20 0.038
269
c CTS034 Cutis Laxa, Autosomal Recessive Type 1 30 0.038
270
MCL055 Mcleod Syndrome with or Without Chronic Granulomatous Disease 22 0.038
271
RDN001 Reading Disorder 39 0.038
272
c VNT026 Ventricular Septal Defect 2 24 0.038
273
CHL028 Childhood Type Dermatomyositis 40 0.038
274
P PLM040 Pulmonary Valve Disease 45 0.038
275
HYD050 Hydrocephalus, Endocardial Fibroelastosis, and Cataracts 16 0.038
276
HYP682 Hypertelorism, Teebi Type 20 0.038
277
c SCL052 Scleroderma, Familial Progressive 27 0.038
278
KNS006 Kniest-Like Dysplasia, Lethal 15 0.038
279
MYT003 Myotonic Disease 33 0.038
280
WLL032 Woolly Hair, Hypotrichosis, Everted Lower Lip, and Outstanding Ears 15 0.038
281
SHP003 Shapiro Syndrome 27 0.038
282
CRN055 Carney Triad 40 0.038
283
MNT002 Mental Depression 52 0.038
284
THL008 Thalamic Degeneration, Symmetric Infantile 13 0.038
285
DXT001 Dextrocardia 44 0.038
286
NTH002 Nathalie Syndrome 23 0.038
287
c DBT082 Diabetes Mellitus, Insulin-Dependent, 12 23 0.038
288
VNT009 Ventricular Tachycardia, Idiopathic 23 0.038
289
MCR088 Microscopic Polyangiitis 47 0.038
290
GDS001 Good Syndrome 46 0.038
291
SBR011 Subaortic Stenosis--Short Stature Syndrome 15 0.038
292
ECT023 Ectodermal Dysplasia, Hidrotic, Christianson-Fourie Type 14 0.038
293
MYC005 Myocardial Stunning 44 0.038
294
c CRD104 Cardiomyopathy, Dilated, 1p 17 0.038
295
HRS003 Hirschsprung Disease Ganglioneuroblastoma 14 0.038
296
PHC013 Phaeochromocytoma 47 0.038
297
HYP037 Hyperhomocysteinemia 49 0.038
298
ALC010 Alcoholic Cardiomyopathy 38 0.038
299
P EXN002 Exanthem 57 0.038
300
CRD023 Cardiomyopathy Cataract Hip Spine Disease 15 0.038
301
c CNT015 Central Sleep Apnea 43 0.038
302
19P001 19p13.12 Microdeletion Syndrome 14 0.038
303
TSH001 Tsh Producing Pituitary Tumor 36 0.038
304
HYP266 Hypoxia 55 0.038
305
SPC003 Specific Developmental Disorder 39 0.038
306
TBT001 Tabatznik Syndrome 16 0.038
307
SBV001 Subvalvular Aortic Stenosis 32 0.038
308
SCN049 Second-Degree Atrioventricular Block 22 0.038
309
PTN008 Patent Arterial Duct 35 0.038
310
CCN002 Cocaine Abuse 47 0.038
311
SPN186 Spinal Cord Injury 62 0.038
312
c DBT056 Diabetes Mellitus, Insulin-Dependent, 4 19 0.038
313
GLC008 Glucose Metabolism Disease 44 0.038
314
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 39 0.038
315
GST007 Gastric Dilatation 38 0.038
316
SNT005 Sinoatrial Node Disease 34 0.038
317
c DBT058 Diabetes Mellitus, Insulin-Dependent, 7 17 0.038
318
APN006 Apnea of Prematurity 20 0.038
319
c ADL079 Adult Heart Tumor 17 0.038
320
MTC028 Mitochondrial Cardiomyopathy 29 0.038
321
CRB004 Cerebral Artery Occlusion 39 0.038
322
PLY127 Polyneuropathy-Intellectual Disability-Acromicria-Premature Menopause Syndrome 12 0.038
323
MND006 Mondor Disease 20 0.038
324
MSC030 Muscular Fibrosis Multifocal Obstructed Vessels 10 0.038
325
BRN106 Burns 52 0.038
326
INT084 Intrinsic Cardiomyopathy 34 0.038
327
PHL007 Philadelphia-Negative Chronic Myeloid Leukemia 22 0.038
328
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.027
329
P AST005 Asthma 80 0.027
330
c MLT019 Multiple Myeloma 77 0.027
331
c AMY091 Amyotrophic Lateral Sclerosis 1 78 0.027
332
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 57 0.027
333
P DRV001 Dravet Syndrome 66 0.027
334
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 61 0.027
335
c DYS166 Dysautonomia, Familial 54 0.027
336
P KDN017 Kidney Cancer 67 0.027
337
P MYP101 Myopathy, Centronuclear 53 0.027
338
KRN002 Kearns-Sayre Syndrome 60 0.027
339
P HLT001 Holt-Oram Syndrome 60 0.027
340
c MLG132 Malignant Hyperthermia Susceptibility 1 34 0.027
341
ANX002 Anxiety Disorder 67 0.027
342
DNN001 Danon Disease 46 0.027
343
P RBN001 Rubinstein-Taybi Syndrome 65 0.027
344
LBR002 Leber Hereditary Optic Neuropathy 59 0.027
345
P DNT015 Dent Disease 61 0.027
346
c TBR024 Tuberous Sclerosis-1 50 0.027
347
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.027
348
P WSK001 Wiskott-Aldrich Syndrome 70 0.027
349
WRN001 Werner Syndrome 69 0.027
350
P TBR001 Tuberous Sclerosis 68 0.027
351
RBR001 Roberts Syndrome 61 0.027
352
CRN183 Carnitine Palmitoyltransferase Ii Deficiency 55 0.027
353
c HRT021 Heart Block, Progressive, Type Ia 46 0.027
354
CRH001 Crohn's Disease 76 0.027
355
MRF001 Marfan Syndrome 73 0.027
356
c MYT020 Myotonic Dystrophy 2 56 0.027
357
KRT002 Keratomalacia 50 0.027
358
P KLF001 Kleefstra Syndrome 41 0.027
359
P HYP366 Hyperkalemic Periodic Paralysis, Type 2 45 0.027
360
MLF002 Malouf Syndrome 40 0.027
361
c DYS170 Dyserythropoietic Anemia, Congenital, Type Ii 29 0.027
362
SCP009 Scapuloperoneal Myopathy, X-Linked Dominant 30 0.027
363
PRD011 Proud Syndrome 42 0.027
364
ULC004 Ulcerative Colitis 74 0.027
365
P RCK004 Rickets 59 0.027
366
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 40 0.027
367
P TMP003 Temporal Arteritis 61 0.027
368
NXS001 Naxos Disease 46 0.027
369
c DYS156 Dyserythropoietic Anemia, Congenital, Type Ia 35 0.027
370
c MSC112 Muscular Dystrophy, Limb-Girdle, Type 1b 27 0.027
371
c ART115 Aortic Valve Disease 1 53 0.027
372
CRT002 Cartilage-Hair Hypoplasia 57 0.027
373
P MTH008 Methylmalonic Acidemia 51 0.027
374
NTR005 Nutritional Deficiency Disease 51 0.027
375
MYP056 Myopathy, X-Linked, with Postural Muscle Atrophy 25 0.027
376
P SMP003 Simpson-Golabi-Behmel Syndrome 46 0.027
377
ADL002 Adult Syndrome 53 0.027
378
P ASP006 Aspergillosis 61 0.027
379
WDH003 Woodhouse-Sakati Syndrome 32 0.027
380
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.027
381
P BRT004 Bartter Disease 46 0.027
382
ULN003 Ulnar-Mammary Syndrome 45 0.027
383
P ALP009 Alopecia Areata 62 0.027
384
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 45 0.027
385
c CRD155 Cardiomyopathy, Dilated, 1kk 27 0.027
386
IVC001 Ivic Syndrome 28 0.027
387
ERL001 Early Myoclonic Encephalopathy 46 0.027
388
c ATM010 Autoimmune Hemolytic Anemia 59 0.027
389
P HYP086 Hypothyroidism 63 0.027
390
c EMR017 Emery-Dreifuss Muscular Dystrophy 1, X-Linked 27 0.027
391
c LNG094 Long Qt Syndrome-10 24 0.027
392
THR013 Thoracic Outlet Syndrome 48 0.027
393
INT088 Intrinsic Factor Deficiency 37 0.027
394
PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 27 0.027
395
P CHL002 Childhood Absence Epilepsy 54 0.027
396
P PHS004 Phosphoribosylpyrophosphate Synthetase Superactivity 39 0.027
397
c VNT010 Ventricular Tachycardia, Catecholaminergic Polymorphic, 2 25 0.027
398
P GT001 Gout 58 0.027
399
P SJG001 Sjogren's Syndrome 55 0.027
400
MDY003 Mody, Type Ii 36 0.027
401
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.027
402
YLL002 Yellow Fever 58 0.027
403
MTC078 Mitochondrial Dna Depletion Syndrome 11 23 0.027
404
c LFT018 Left Ventricular Noncompaction 10 23 0.027
405
PRN037 Prinzmetal's Variant Angina 30 0.027
406
P LMB006 Limb-Girdle Muscular Dystrophy 54 0.027
407
c BRG009 Brugada Syndrome 7 23 0.027
408
MYT022 Myotubular Myopathy, X-Linked 32 0.027
409
c CRD097 Cardiomyopathy, Dilated, 1d 24 0.027
410
LVR012 Liver Cirrhosis 71 0.027
411
P GRV001 Graves' Disease 62 0.027
412
MTN003 Motion Sickness 48 0.027
413
CHR543 Chromosome 2q37 Deletion Syndrome 30 0.027
414
P PLY017 Polyarteritis Nodosa 54 0.027
415
c CRD187 Cardiomyopathy, Dilated, 3b 40 0.027
416
c CNG006 Congenital Hypothyroidism 59 0.027
417
c JRV002 Jervell and Lange-Nielsen Syndrome 2 25 0.027
418
GTR002 Goiter 54 0.027
419
P THL005 Thalassemia 61 0.027
420
LFT013 Left Ventricular Noncompaction 1, with or Without Congenital Heart Defects 23 0.027
421
c CCK006 Cockayne Syndrome, Type B 37 0.027
422
P HYP055 Hypoplastic Left Heart Syndrome 60 0.027
423
SDD002 Sudden Infant Death with Dysgenesis of the Testes Syndrome 25 0.027
424
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 54 0.027
425
ARR037 Arrhythmogenic Right Ventricular Dysplasia 12 23 0.027
426
END020 Endocardial Fibroelastosis 44 0.027
427
TYP007 Typhoid Fever 61 0.027
428
c DNT021 Dent Disease 2 37 0.027
429
MYP092 Myopathy, Early-Onset, with Fatal Cardiomyopathy 22 0.027
430
c CRD190 Cardiomyopathy, Hypertrophic, 2 29 0.027
431
OLV001 Olivopontocerebellar Atrophy 53 0.027
432
MDY006 Mody, Type Iv 31 0.027
433
c HMC021 Hemochromatosis, Type 2a 29 0.027
434
c CRD198 Cardiomyopathy, Hypertrophic, 18 26 0.027
435
CHR515 Chronic Atrial and Intestinal Dysrhythmia 19 0.027
436
c CRD206 Cardiomyopathy, Hypertrophic, 11 23 0.027
437
P MTR012 Mitral Valve Disease 59 0.027
438
c ATR038 Atrial Fibrillation, Familial, 3 27 0.027
439
CMB025 Combined Oxidative Phosphorylation Deficiency 10 21 0.027
440
c CCK005 Cockayne Syndrome, Type a 39 0.027
441
c LCL006 Localized Scleroderma 60 0.027
442
SPC010 Speech and Communication Disorders 42 0.027
443
c EMR012 Emery-Dreifuss Muscular Dystrophy 3, Ar 21 0.027
444
MTC088 Mitochondrial Dna Depletion Syndrome 13 24 0.027
445
EBS001 Ebstein Anomaly 44 0.027
446
c PRM005 Primary Hyperparathyroidism 56 0.027
447
c CRD063 Cardiomyopathy, Dilated, 2a 25 0.027
448
ESN020 Eosinophilic Granulomatosis with Polyangiitis 38 0.027
449
P HRT035 Heart Block, Congenital 40 0.027
450
P MNN013 Meningitis 66 0.027
451
GST037 Gastroparesis 54 0.027
452
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 34 0.027
453
c DYS145 Dystonia 23 24 0.027
454
HMN035 Hemangioma-Thrombocytopenia Syndrome 25 0.027
455
c BRG004 Brugada Syndrome 4 21 0.027
456
c CRD112 Cardiomyopathy, Dilated, 1u 22 0.027
457
c CRD162 Cardiomyopathy, Dilated, 1ii 22 0.027
458
CHL068 Cholestasis 57 0.027
459
CGN006 Cogan Syndrome 48 0.027
460
ALN001 Aland Island Eye Disease 45 0.027
461
IMP005 Impotence 49 0.027
462
c CRD080 Cardiomyopathy, Dilated, 1g 22 0.027
463
HYP022 Hypohidrosis 41 0.027
464
c PND001 Pain Disorder 53 0.027
465
PLM041 Pulmonary Valve Stenosis 48 0.027
466
c CRD149 Cardiomyopathy, Dilated, 1jj 30 0.027
467
TRN015 Transient Cerebral Ischemia 57 0.027
468
P RST002 Restrictive Cardiomyopathy 48 0.027
469
c CRD153 Cardiomyopathy, Dilated, 2b 22 0.027
470
c CRD060 Cardiomyopathy, Dilated, 1z 21 0.027
471
c CRD064 Cardiomyopathy, Dilated, 1ff 21 0.027
472
P HYP069 Hyperparathyroidism 57 0.027
473
c BRG006 Brugada Syndrome 2 31 0.027
474
c EMR015 Emery-Dreifuss Muscular Dystrophy 5, Autosomal Dominant 20 0.027
475
c ATR068 Atrial Fibrillation, Familial, 14 21 0.027
476
CDS001 Cadasil 50 0.027
477
PRP007 Priapism 48 0.027
478
c CNG464 Congenital Myopathy 49 0.027
479
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.027
480
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 35 0.027
481
DBT074 Diabetes, Mellitus, Insulin-Dependent 10 19 0.027
482
c LNG096 Long Qt Syndrome 15 42 0.027
483
c LNG098 Long Qt Syndrome 14 42 0.027
484
PRT030 Parathyroid Gland Disease 49 0.027
485
P HYP004 Hypercalcemia 54 0.027
486
ACT098 Acute Erythroid Leukemia 34 0.027
487
c CRD082 Cardiomyopathy, Dilated, 1gg 30 0.027
488
STT002 Status Asthmaticus 43 0.027
489
FRY001 Frey Syndrome 38 0.027
490
CRD191 Cardiomyopathy, Dilated, 1aa, with or Without Lvnc 20 0.027
491
c EMR011 Emery-Dreifuss Muscular Dystrophy 2, Ad 36 0.027
492
CMB054 Combined Oxidative Phosphorylation Deficiency 23 20 0.027
493
P DRR001 Diarrhea 60 0.027
494
P SYP003 Syphilis 51 0.027
495
TNS005 Tonsillitis 58 0.027
496
c VNT012 Ventricular Fibrillation, Paroxysmal Familial, 2 15 0.027
497
c SCK022 Sick Sinus Syndrome 3 20 0.027
498
TRT015 Torticollis, Keloids, Cryptorchidism, and Renal Dysplasia 19 0.027
499
NSY001 N Syndrome 42 0.027
500
THY030 Thyroid Gland Disease 52 0.027
501
RLP001 Relapsing Polychondritis 52 0.027
502
RGH009 Right Atrial Isomerism 31 0.027
503
ANT018 Anthracosis 41 0.027
504
LRN003 Learning Disability 49 0.027
505
c PRG101 Progressive Familial Heart Block, Type Ii 23 0.027
506
CTS011 Cutis Marmorata Telangiectatica Congenita 31 0.027
507
BRM003 Biermer's Disease 22 0.027
508
LNS003 Lens Disease 37 0.027
509
P EMR004 Emery-Dreifuss Muscular Dystrophy, X-Linked 27 0.027
510
CLS010 Cluster Headache 43 0.027
511
CNG134 Congenitally Corrected Transposition of the Great Arteries 25 0.027
512
CNN005 Connective Tissue Disease 60 0.027
513
TTR024 Tetramelic Deficiencies, Ectodermal Dysplasia, Deformed Ears, and Other Abnormalities 21 0.027
514
NWC001 Newcastle Disease 51 0.027
515
MYF002 Myofascial Pain Syndrome 38 0.027
516
TRN012 Transient Global Amnesia 38 0.027
517
c CRD102 Cardiomyopathy, Dilated, 1j 19 0.027
518
MGR035 Migraine with Brainstem Aura 16 0.027
519
c AST037 Asthma 1 35 0.027
520
c AST039 Asthma 2 28 0.027
521
GLS004 Glossopharyngeal Neuralgia 33 0.027
522
c ACT071 Acute Kidney Failure 48 0.027
523
PRM201 Primary Hypomagnesemia with Secondary Hypocalcemia 17 0.027
524
RTN072 Retinohepatoendocrinologic Syndrome 26 0.027
525
DDN006 Duodenitis 44 0.027
526
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.027
527
c CNG404 Congenital Heart Defects, Multiple Types, 4 27 0.027
528
PNN001 Panniculitis 47 0.027
529
END021 Endomyocardial Fibrosis 47 0.027
530
PGD001 Pagod Syndrome 21 0.027
531
P AMY004 Amyloidosis 63 0.027
532
MCH010 Michels Syndrome 24 0.027
533
c CRD101 Cardiomyopathy, Dilated, 1x 20 0.027
534
LNG102 Long-Thumb Brachydactyly Syndrome 13 0.027
535
P MTR041 Mitral Valve Prolapse, Myxomatous 2 16 0.027
536
c CNG012 Congenital Generalized Lipodystrophy 42 0.027
537
ANH002 Anhidrosis 42 0.027
538
PRP021 Peripheral Nervous System Neoplasm 49 0.027
539
PST048 Postural Orthostatic Tachycardia Syndrome 29 0.027
540
c CRD091 Cardiomyopathy, Dilated, 1dd 21 0.027
541
c CRD113 Cardiomyopathy, Dilated, 1v 18 0.027
542
c CRD159 Cardiomyopathy, Dilated, 1hh 17 0.027
543
HYP540 Hypertension, Diastolic 40 0.027
544
AGR002 Agoraphobia 41 0.027
545
SXL003 Sexual Disorder 45 0.027
546
c CRD090 Cardiomyopathy, Dilated, 1l 17 0.027
547
c CRD105 Cardiomyopathy, Dilated, 1o 17 0.027
548
DFN007 Deafness Enamel Hypoplasia Nail Defects 24 0.027
549
BLL007 Bullous Skin Disease 39 0.027
550
NN2002 Non 24 Hour Sleep Wake Disorder 23 0.027
551
DRG003 Drug Dependence 53 0.027
552
END040 Endogenous Depression 51 0.027
553
CRN017 Coronary Thrombosis 46 0.027
554
ADN002 Adenoiditis 38 0.027
555
BRN055 Bronchogenic Cyst 27 0.027
556
LFT009 Left Ventricular Outflow Tract Obstruction 43 0.027
557
HYP611 Hypoparathyroidism, X-Linked 21 0.027
558
TRC062 Tricuspid Atresia 34 0.027
559
INF034 Infective Endocarditis 50 0.027
560
c CRD092 Cardiomyopathy, Dilated, 1w 16 0.027
561
c CRD096 Cardiomyopathy, Dilated, 1ee 16 0.027
562
c CRD103 Cardiomyopathy, Dilated, 1t 21 0.027
563
c CRD108 Cardiomyopathy, Dilated, 1bb 16 0.027
564
c CRD111 Cardiomyopathy, Dilated, 1i 17 0.027
565
c CRD114 Cardiomyopathy, Dilated, 1m 20 0.027
566
c CRD115 Cardiomyopathy, Dilated, 1cc 16 0.027
567
FCT008 Factitious Disorder 42 0.027
568
ADJ001 Adjustment Disorder 38 0.027
569
SKN005 Skin Atrophy 42 0.027
570
GRW007 Growth Hormone Deficiency 49 0.027
571
P END033 Endocarditis 52 0.027
572
FDB001 Foodborne Botulism 34 0.027
573
TRY001 Trypanosomiasis 51 0.027
574
PLM008 Pulmonary Subvalvular Stenosis 16 0.027
575
THR099 Third-Degree Atrioventricular Block 31 0.027
576
P LPD010 Lipodystrophy 51 0.027
577
VSC009 Vascular Skin Disease 21 0.027
578
CRD001 Cardiac Tamponade 43 0.027
579
CTN032 Cutaneous Mastocytosis, Conductive Hearing Loss and Microtia 14 0.027
580
P PSD015 Pseudohypoparathyroidism 43 0.027
581
VNT031 Ventricular Extrasystoles with Syncope, Perodactyly, and Robin Sequence 14 0.027
582
LWN001 Lown-Ganong-Levine Syndrome 28 0.027
583
DRG014 Drug-Induced Autoimmune Hemolytic Anemia 17 0.027
584
GND003 Gonadal Disease 41 0.027
585
AGG002 Aggressive Systemic Mastocytosis 42 0.027
586
EXT058 Extrasystoles, Multiform Ventricular, with Short Stature, Hyperpigmentation and Microcephaly 14 0.027
587
c LMB067 Limb-Girdle Muscular Dystrophy 2x 13 0.027
588
PHY002 Physical Disorder 43 0.027
589
HRY002 Hairy Tongue 23 0.027
590
CRB008 Cerebral Atherosclerosis 37 0.027
591
20P001 20p12.3 Microdeletion Syndrome 13 0.027
592
RBB001 Ribbing Disease 14 0.027
593
ATM069 Autoimmune Hemolytic Anemia, Warm Type 19 0.027
594
BLC017 Black Hairy Tongue 16 0.027
595
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 21 0.027
596
c ALP005 Alpha Chain Disease 36 0.027
597
CLC007 Calcium Metabolism Disease 39 0.027
598
c SCN006 Secondary Syphilis 41 0.027
599
P CRV039 Cervicitis 45 0.027
600
ATN003 Autonomic Nervous System Neoplasm 43 0.027
601
P DYS021 Dysautonomia 47 0.027
602
INT010 Intracranial Embolism 32 0.027
603
RNL097 Renal Artery Disease 44 0.027
604
P PNM006 Pneumoconiosis 51 0.027
605
MNN032 Meningococcal Meningitis 33 0.027
606
DMD003 Dmd-Associated Dilated Cardiomyopathy 11 0.027
607
ART004 Aortic Atherosclerosis 46 0.027
608
WLD005 Wild Type Attr Amyloidosis 18 0.027
609
c ATR025 Atrial Fibrillation, Familial, 2 16 0.027
610
CRT008 Carotid Artery Dissection 38 0.027
611
ESN011 Eisenmenger Syndrome 45 0.027
612
PLM068 Pulmonary Vein Stenosis 39 0.027
613
P RNL015 Renal Hypertension 47 0.027
614
PRP080 Peripheral Artery Disease 35 0.027
615
c HYP453 Hypertension, Essential 7 14 0.027
616
NSP003 Nasopharyngeal Disease 25 0.027
617
THL017 Thalassemia Intermedia 38 0.027
618
BLD054 Blood Protein Disease 38 0.027
619
ADR009 Adrenal Cortex Disease 40 0.027
620
HRT029 Heart Tumor of the Child 16 0.027
621
KDN013 Kidney Hypertrophy 32 0.027
622
P ATR081 Atrial Standstill 29 0.027
623
c FML272 Familial Sick Sinus Syndrome 30 0.027
624
ANR042 Aniridia - Ptosis - Intellectual Disability - Familial Obesity 9 0.027
625
BRN080 Brain Ischemia 42 0.027
626
INF133 Inferior Vena Cava Interruption 28 0.027
627
PLM060 Pulmonary Branches Stenosis 6 0.027
628
P PSD003 Pseudohypoaldosteronism 42 0.027
629
c CNG031 Congenital Nervous System Abnormality 39 0.027
630
CRB031 Cerebral Arterial Disease 31 0.027
631
EPL095 Epilepsy with Myoclonic Absences 13 0.027
632
P ACT080 Acute Pulmonary Heart Disease 31 0.027
633
INT074 Intracranial Arteriosclerosis 14 0.027
634
NRN002 Neuronitis 40 0.027
635
DPH006 Diaphragmatic Eventration 28 0.027
636
c RNL016 Renal Infectious Disease 22 0.027
637
EYC003 Eye Accommodation Disease 25 0.027
638
c INV001 Invasive Aspergillosis 44 0.027
639
PLY088 Polyvalvular Heart Disease Syndrome 12 0.027
640
IDP076 Idiopathic Ventricular Fibrillation, Not Brugada Type 8 0.027
641
MXD035 Mixed-Type Autoimmune Hemolytic Anemia 18 0.027
642
WTH001 Withdrawal Disorder 36 0.027
643
c CHR096 Chronic Pulmonary Heart Disease 40 0.027
644
INT062 Interstitial Myocarditis 22 0.027
645
SBN001 Subendocardial Myocardial Infarction 33 0.027
646
TXC010 Toxic Myocarditis 28 0.027
647
c ATM022 Autoimmune Myocarditis 39 0.027
648
CRB087 Cerebral Arteriosclerosis 23 0.027
649
CRN208 Coronary Sinus Atresia 8 0.027
650
DGT004 Digitalis Poisoning 11 0.027
651
c EMR003 Emery-Dreifuss Muscular Dystrophy, Dominant Type 16 0.027
652
ARR005 Arrhythmogenic Right Ventricular Dysplasia/cardiomyopathy 2 11 0.027
653
ARR006 Arrhythmogenic Right Ventricular Dysplasia/cardiomyopathy 3 9 0.027
654
ARR008 Arrhythmogenic Right Ventricular Dysplasia/cardiomyopathy 5 11 0.027
655
ARR009 Arrhythmogenic Right Ventricular Dysplasia/cardiomyopathy 6 8 0.027
656
ARR011 Arrhythmogenic Right Ventricular Dysplasia/cardiomyopathy 8 7 0.027
657
END072 Endotheliitis 41 0.027
658
BRN071 Brain Injury 51 0.027
659
THL018 Thalassemia Major 31 0.027
660
DXR001 Doxorubicin Induced Cardiomyopathy 36 0.027
661
P FML187 Familial Hypertension 35 0.027
662
FTT003 Fatty Acid Oxidation Disorders 38 0.027
663
ART033 Aortic Valves Stenosis of the Child 8 0.027
664
VSC047 Vascular Malformation 45 0.027