Search results for "ventricular tachycardia"

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

408 hits were found for 'ventricular tachycardia'

# Family MCID Name MIFTS Score
1
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 58 12.242
2
c VNT013 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1 49 8.656
3
c VNT029 Ventricular Tachycardia, Catecholaminergic Polymorphic, 4 41 8.034
4
c VNT010 Ventricular Tachycardia, Catecholaminergic Polymorphic, 2 36 7.744
5
VNT009 Ventricular Tachycardia, Idiopathic 18 4.831
6
VNT025 Ventricular Tachycardia, Catecholaminergic Polymorphic, 5, with or Without Muscle Weakness 15 4.319
7
c VNT027 Ventricular Tachycardia, Catecholaminergic Polymorphic, 3 15 4.315
8
BDR001 Bidirectional Tachycardia 14 3.359
9
c CLM002 Calm1-Related Catecholaminergic Polymorphic Ventricular Tachycardia 11 3.068
10
INC014 Incessant Infant Ventricular Tachycardia 3 3.063
11
c CRD105 Cardiomyopathy, Dilated, 1o 23 3.026
12
c CTC003 Catecholaminergic Polymorphic Ventricular Tachycardia 5 8 2.213
13
c CSQ001 Casq2-Related Catecholaminergic Polymorphic Ventricular Tachycardia 6 2.170
14
c RYR003 Ryr2-Related Catecholaminergic Polymorphic Ventricular Tachycardia 6 2.170
15
c TRD007 Trdn-Related Catecholaminergic Polymorphic Ventricular Tachycardia 6 2.170
16
c ABC013 Abcc9-Related Dilated Cardiomyopathy 11 2.120
17
P CRD011 Cardiomyopathy 67 0.614
18
P VNT002 Ventricular Septal Defect 59 0.439
19
P HRT032 Heart Disease 76 0.428
20
P MYC007 Myocardial Infarction 79 0.418
21
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 0.402
22
SNG003 Single Ventricular Heart 24 0.336
23
LFT009 Left Ventricular Outflow Tract Obstruction 44 0.299
24
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 55 0.298
25
P LFT003 Left Ventricular Noncompaction 49 0.294
26
RGH001 Right Bundle Branch Block 43 0.286
27
CNG034 Congestive Heart Failure 71 0.286
28
TRN044 Transposition of the Great Arteries 47 0.268
29
P ATR011 Atrial Fibrillation 64 0.261
30
c CRN175 Coronary Heart Disease 4 21 0.257
31
TTR001 Tetralogy of Fallot 71 0.257
32
CRD003 Cardiac Sarcoidosis 43 0.254
33
SYN036 Syncope 47 0.250
34
P CRN178 Coronary Heart Disease 6 24 0.247
35
ANR040 Aneurysm 57 0.247
36
c DLT002 Dilated Cardiomyopathy 75 0.246
37
c CRN172 Coronary Heart Disease 3 21 0.246
38
WLF001 Wolff-Parkinson-White Syndrome 57 0.246
39
ATR060 Atrial Standstill, Digenic 53 0.237
40
P BRG001 Brugada Syndrome 59 0.236
41
c ACT075 Acute Myocardial Infarction 60 0.231
42
P MYC008 Myocarditis 54 0.218
43
ISC004 Ischemia 59 0.213
44
c CRN174 Coronary Heart Disease 2 22 0.208
45
P CRN211 Coronary Artery Disease 75 0.202
46
ISC006 Ischemic Heart Disease 68 0.201
47
c CRN214 Coronary Heart Disease 5 23 0.198
48
ATR057 Atrioventricular Block 49 0.194
49
SYS003 Systolic Heart Failure 43 0.179
50
SDD007 Sudden Cardiac Death 46 0.177
51
INF013 Inferior Myocardial Infarction 37 0.176
52
VNT011 Ventricular Fibrillation, Familial, 1 43 0.173
53
ART111 Artery Disease 57 0.171
54
P PLM037 Pulmonary Hypertension 79 0.171
55
CRD119 Cardiac Arrest 63 0.170
56
CRD137 Cardiogenic Shock 46 0.170
57
ATN005 Autonomic Dysfunction 45 0.169
58
P ORT004 Orthostatic Intolerance 65 0.162
59
P SCK002 Sick Sinus Syndrome 50 0.157
60
ATN002 Autonomic Nervous System Disease 47 0.156
61
P PRX010 Paroxysmal Ventricular Fibrillation 39 0.155
62
c FML001 Familial Atrial Fibrillation 59 0.155
63
DST006 Diastolic Heart Failure 46 0.154
64
TRC062 Tricuspid Atresia 34 0.151
65
CNG134 Congenitally Corrected Transposition of the Great Arteries 23 0.150
66
DXT001 Dextrocardia 44 0.145
67
PRP009 Peripartum Cardiomyopathy 41 0.145
68
PRN021 Paranasal Sinus Disease 50 0.142
69
NSL022 Nasal Cavity Disease 42 0.142
70
PRP027 Peripheral Vascular Disease 69 0.140
71
P CRD132 Cardiac Conduction Defect 40 0.138
72
ADL002 Adult Syndrome 53 0.136
73
P DYS021 Dysautonomia 47 0.133
74
c CRN176 Coronary Heart Disease 9 20 0.132
75
SNT004 Sinoatrial Node Dysfunction and Deafness 27 0.131
76
PLM033 Pulmonary Embolism 59 0.130
77
c HYP595 Hypertension, Essential 69 0.126
78
ART021 Arteriosclerosis 59 0.125
79
HYP005 Hypokalemia 51 0.124
80
c MYC058 Myocardial Infarction 2 29 0.123
81
HRT008 Heart Conduction Disease 43 0.120
82
HYD012 Hydrops Fetalis 44 0.119
83
P END033 Endocarditis 52 0.116
84
PRC013 Pericarditis 52 0.115
85
c ACT076 Acute Myocarditis 42 0.114
86
P MSC005 Muscular Dystrophy 64 0.112
87
CRN030 Coronary Stenosis 50 0.112
88
P MTR012 Mitral Valve Disease 59 0.111
89
STR067 Stroke, Ischemic 77 0.111
90
c CRN177 Coronary Heart Disease 7 22 0.110
91
UNV002 Univentricular Heart 26 0.110
92
P MYP004 Myopathy 67 0.109
93
END074 Endocardium Disease 26 0.109
94
P MYT002 Myotonic Dystrophy 47 0.109
95
GNT019 Giant Cell Myocarditis 31 0.109
96
P MSC007 Muscle Hypertrophy 59 0.108
97
INT007 Intermediate Coronary Syndrome 52 0.107
98
HSB001 His Bundle Tachycardia 22 0.107
99
VND001 Vein Disease 52 0.107
100
ART031 Aortic Coarctation 42 0.107
101
CHT001 Chaotic Atrial Tachycardia 7 0.105
102
EBS001 Ebstein Anomaly 44 0.103
103
AND005 Androgen Insensitivity Syndrome, Mild 16 0.102
104
ACR041 Acromelic Frontonasal Dysostosis 46 0.101
105
FNT004 Fainting 33 0.101
106
BRT030 Birth Defects 43 0.100
107
P RSP003 Respiratory Failure 70 0.099
108
ART017 Aortic Disease 58 0.097
109
NXS001 Naxos Disease 44 0.095
110
HPT074 Hepatic Adenoma, Somatic 51 0.094
111
MSC004 Muscle Tissue Disease 36 0.094
112
P PHC003 Pheochromocytoma 71 0.094
113
CRB009 Cerebritis 38 0.093
114
HNM002 Hinman Syndrome 25 0.093
115
FBR012 Fabry Disease 69 0.092
116
END072 Endotheliitis 42 0.092
117
KDS001 Kid Syndrome 53 0.091
118
ARR026 Arrhythmogenic Right Ventricular Dysplasia 1 29 0.091
119
CRT028 Cor Triatriatum 21 0.091
120
ALR002 Al-Raqad Syndrome 36 0.090
121
P AMY004 Amyloidosis 64 0.090
122
ANG054 Angina Pectoris 51 0.090
123
CHL071 Child Syndrome 58 0.089
124
P OBS005 Obesity 93 0.088
125
VSC007 Vascular Disease 67 0.088
126
MRF001 Marfan Syndrome 73 0.088
127
ARR030 Arrhythmogenic Right Ventricular Dysplasia 2 29 0.087
128
ARR025 Arrhythmogenic Right Ventricular Dysplasia 5 27 0.087
129
CHR066 Chronic Fatigue Syndrome 64 0.086
130
CNS002 Constrictive Pericarditis 34 0.086
131
PCK002 Pick Disease 67 0.086
132
CHG001 Chagas Disease 62 0.085
133
END020 Endocardial Fibroelastosis 44 0.085
134
c MTR002 Mitral Valve Insufficiency 44 0.085
135
P THY032 Thyroiditis 54 0.084
136
c CRN173 Coronary Heart Disease 8 20 0.084
137
P NRP001 Neuropathy 60 0.083
138
RSP006 Respiratory System Disease 62 0.083
139
c SHR030 Short Qt Syndrome 43 0.083
140
ARR037 Arrhythmogenic Right Ventricular Dysplasia 12 25 0.082
141
SNT005 Sinoatrial Node Disease 35 0.082
142
INF034 Infective Endocarditis 50 0.082
143
STR037 Stress Cardiomyopathy 36 0.082
144
c SCK017 Sick Sinus Syndrome 1 29 0.081
145
ESN011 Eisenmenger Syndrome 44 0.080
146
HYP540 Hypertension, Diastolic 41 0.080
147
CRN017 Coronary Thrombosis 48 0.079
148
SLP005 Sleep Disorder 53 0.079
149
P EPL164 Epilepsy 66 0.078
150
P RST002 Restrictive Cardiomyopathy 50 0.077
151
ARR029 Arrhythmogenic Right Ventricular Dysplasia 8 24 0.077
152
c LNG044 Long Qt Syndrome 1 67 0.077
153
BLD053 Blood Platelet Disease 46 0.077
154
PTN001 Patent Foramen Ovale 54 0.076
155
MYC005 Myocardial Stunning 44 0.076
156
ARR040 Arrhythmogenic Right Ventricular Dysplasia 10 28 0.076
157
P MSC033 Muscle Disorders 52 0.075
158
DCH001 Duchenne Muscular Dystrophy 80 0.073
159
BRN106 Burns 52 0.072
160
CRD001 Cardiac Tamponade 44 0.072
161
ATN004 Autonomic Neuropathy 44 0.070
162
c CRD099 Cardiomyopathy, Dilated, 1e 42 0.070
163
MDS022 Mediastinitis 41 0.070
164
CHR413 Chronic Myocardial Ischemia 40 0.070
165
ARR041 Arrhythmogenic Right Ventricular Dysplasia, Familial, 13 20 0.070
166
P LYM118 Lymphoma 70 0.070
167
LPM004 Lipoma 58 0.070
168
P HYP076 Hyperthyroidism 56 0.070
169
CST001 Costello Syndrome 69 0.069
170
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 41 0.069
171
P BPL003 Bipolar Disorder 62 0.068
172
NRN002 Neuronitis 42 0.068
173
c SCK014 Sick Sinus Syndrome 2 27 0.068
174
P MNN013 Meningitis 65 0.067
175
ADJ001 Adjustment Disorder 38 0.067
176
TXC005 Toxic Shock Syndrome 61 0.067
177
P THY054 Thyrotoxic Periodic Paralysis 47 0.066
178
HTR003 Heterotaxy 42 0.066
179
P HRT035 Heart Block, Congenital 39 0.066
180
P RNL015 Renal Hypertension 47 0.066
181
ARR036 Arrhythmogenic Right Ventricular Dysplasia 3 15 0.066
182
ARR034 Arrhythmogenic Right Ventricular Dysplasia 6 13 0.066
183
WLL006 Wells Syndrome 56 0.064
184
GDS001 Good Syndrome 45 0.064
185
ART016 Aortic Aneurysm 67 0.064
186
HYP266 Hypoxia 55 0.062
187
HRT007 Heart Cancer 50 0.062
188
P HRT017 Heart Tumor 35 0.062
189
c ADL079 Adult Heart Tumor 19 0.062
190
ANR010 Aneurysm of Sinus of Valsalva 25 0.062
191
P DRM010 Dermatomyositis 58 0.061
192
LPD004 Lipoid Nephrosis 48 0.061
193
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.061
194
ACR007 Acromegaly 65 0.061
195
c BLD124 Bleeding Disorder, Platelet-Type, 11 42 0.061
196
PRP080 Peripheral Artery Disease 36 0.061
197
c PST001 Posterior Myocardial Infarction 32 0.061
198
PPL022 Papilloma 55 0.059
199
ARR008 Arrhythmogenic Right Ventricular Dysplasia/cardiomyopathy 5 13 0.059
200
ARR009 Arrhythmogenic Right Ventricular Dysplasia/cardiomyopathy 6 10 0.059
201
P SHR029 Short Syndrome 60 0.058
202
c PND001 Pain Disorder 55 0.058
203
P CHR345 Chronic Pain 49 0.058
204
PST055 Postural Hypotension 37 0.058
205
c SCK022 Sick Sinus Syndrome 3 22 0.057
206
P ALX003 Alexander Disease 64 0.057
207
P AND016 Andersen Syndrome 58 0.057
208
c THR092 Thrombophilia Due to Thrombin Defect 56 0.057
209
P BLD051 Blood Coagulation Disease 45 0.057
210
ARR005 Arrhythmogenic Right Ventricular Dysplasia/cardiomyopathy 2 13 0.057
211
ARR006 Arrhythmogenic Right Ventricular Dysplasia/cardiomyopathy 3 11 0.057
212
KWS002 Kawasaki Disease 70 0.055
213
BCK001 Becker Muscular Dystrophy 68 0.055
214
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 55 0.055
215
CRD118 Cardiovascular Cancer 47 0.055
216
PDT040 Pediatric Hypertension 31 0.055
217
P PLM064 Pulmonary Sequestration 26 0.055
218
FML213 Familial Isolated Arrhythmogenic Ventricular Dysplasia, Right Dominant Form 24 0.055
219
ATR055 Atrial Septal Aneurysm 24 0.055
220
ATR024 Atrial Fibrillation and Stroke 22 0.055
221
DBL010 Double-Orifice Mitral Valve 16 0.055
222
EXF001 Exfoliation Syndrome 57 0.055
223
P PRP019 Peripheral Nervous System Disease 54 0.055
224
P PLN008 Peeling Skin Syndrome 47 0.055
225
ANX002 Anxiety Disorder 69 0.054
226
MLG056 Malignant Hyperthermia 57 0.054
227
NWC001 Newcastle Disease 54 0.054
228
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 44 0.054
229
c FML191 Familial Long Qt Syndrome 41 0.054
230
NTR005 Nutritional Deficiency Disease 39 0.054
231
P AST005 Asthma 82 0.053
232
P NRV007 Nervous System Disease 71 0.053
233
CSY001 C Syndrome 49 0.053
234
ALN001 Aland Island Eye Disease 45 0.053
235
FCT008 Factitious Disorder 43 0.053
236
INT084 Intrinsic Cardiomyopathy 35 0.053
237
ARR004 Arrhythmogenic Right Ventricular Dysplasia/cardiomyopathy 1 12 0.053
238
PRV004 Periventricular Leukomalacia 48 0.051
239
LPM005 Lipomatosis 47 0.051
240
CRN019 Coronary Artery Vasospasm 42 0.051
241
PRD011 Proud Syndrome 42 0.051
242
LKM006 Leukomalacia 42 0.051
243
CNV002 Conversion Disorder 42 0.051
244
NTR041 N-Terminal Acetyltransferase Deficiency 32 0.051
245
P ATX010 Ataxia Neuropathy Spectrum 28 0.051
246
P ATX004 Ataxia 53 0.051
247
PHY002 Physical Disorder 44 0.051
248
CRB085 Cerebral Hemorrhage 43 0.051
249
BRN080 Brain Ischemia 41 0.051
250
CRD180 Cardiomyopathy, Dilated, with Woolly Hair and Keratoderma 35 0.051
251
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 34 0.051
252
c CRD204 Cardiomyopathy, Hypertrophic, 10 29 0.051
253
FML214 Familial Isolated Arrhythmogenic Ventricular Dysplasia, Biventricular Form 23 0.051
254
FML215 Familial Isolated Arrhythmogenic Ventricular Dysplasia, Left Dominant Form 23 0.051
255
VNT031 Ventricular Extrasystoles with Syncope, Perodactyly, and Robin Sequence 13 0.051
256
LYM017 Lyme Disease 63 0.050
257
STT001 Status Epilepticus 59 0.050
258
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 29 0.050
259
DFC004 Deficiency Anemia 65 0.048
260
HYP066 Hyperglycemia 60 0.048
261
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.048
262
CTS003 Coats Disease 57 0.048
263
BRN071 Brain Injury 52 0.048
264
NSD001 Nose Disease 52 0.048
265
PRT011 Protein C Deficiency 51 0.048
266
LRN003 Learning Disability 51 0.048
267
P MYF003 Myofibrillar Myopathy 38 0.048
268
c AST037 Asthma 1 31 0.048
269
FRS012 First-Degree Atrioventricular Block 31 0.048
270
PRT048 Partial Atrioventricular Canal 30 0.048
271
MTR027 Mitral Atresia 16 0.048
272
P MYS003 Myasthenia Gravis 65 0.048
273
CMM005 Common Cold 58 0.048
274
GTR002 Goiter 54 0.048
275
IRN001 Iron Deficiency Anemia 51 0.048
276
P HYP071 Hypersensitivity Reaction Type Ii Disease 51 0.048
277
HYP017 Hypophosphatemia 42 0.048
278
BCK006 Back Pain 42 0.048
279
MYX004 Myxedema 38 0.048
280
BRN105 Burn Scar 37 0.048
281
c PLN017 Peeling Skin Syndrome 1 33 0.048
282
CNT017 Central Nervous System Origin Vertigo 28 0.048
283
BRN028 Brain Cancer 70 0.045
284
DWN001 Down Syndrome 65 0.045
285
P FRD001 Friedreich Ataxia 62 0.045
286
NRM005 Neuromuscular Disease 57 0.045
287
FBR054 Fibroma 43 0.045
288
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.045
289
CRN041 Carnitine-Acylcarnitine Translocase Deficiency 42 0.045
290
BLD054 Blood Protein Disease 40 0.045
291
SPC003 Specific Developmental Disorder 40 0.045
292
RDN001 Reading Disorder 39 0.045
293
NSY001 N Syndrome 39 0.045
294
P LNG092 Long Qt Syndrome-3 35 0.045
295
c CRD202 Cardiomyopathy, Hypertrophic, 12 29 0.045
296
SPN331 Spondyloocular Syndrome 27 0.045
297
CRD054 Cardiac Arrhythmia, Ankyrin-B-Related 22 0.045
298
BRR004 Baroreflex Failure 21 0.045
299
LVC002 Levocardia 18 0.045
300
HRT029 Heart Tumor of the Child 17 0.045
301
P NRM001 Neuromyelitis Optica 59 0.043
302
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.043
303
UND005 Undifferentiated Pleomorphic Sarcoma 43 0.043
304
ATM052 Autoimmune Disease 1 28 0.043
305
c SHR033 Short Qt Syndrome 3 27 0.043
306
ATR048 Atrial Tachyarrhythmia with Short Pr Interval 27 0.043
307
ATM013 Autoimmune Disease of Cardiovascular System 15 0.043
308
DGT004 Digitalis Poisoning 11 0.043
309
P BRS047 Breast Cancer 100 0.042
310
P LKM002 Leukemia 70 0.042
311
PLM129 Pulmonary Disease, Chronic Obstructive 62 0.042
312
P EXN002 Exanthem 57 0.042
313
CND002 Conduct Disorder 56 0.042
314
P MYS005 Myositis 56 0.042
315
MVM001 Movement Disease 54 0.042
316
GST050 Gastrointestinal System Disease 54 0.042
317
P LMY004 Leiomyosarcoma 53 0.042
318
TRM010 Traumatic Brain Injury 52 0.042
319
P JRV003 Jervell and Lange-Nielsen Syndrome 52 0.042
320
QDR001 Quadriplegia 52 0.042
321
GNR004 Generalized Anxiety Disorder 51 0.042
322
CRC006 Carcinoid Syndrome 51 0.042
323
RHM028 Rheumatic Heart Disease 51 0.042
324
LMB062 Limb Ischemia 48 0.042
325
PLN006 Poland Syndrome 48 0.042
326
HMN009 Hemangioblastoma 45 0.042
327
PHC013 Phaeochromocytoma 41 0.042
328
c PRG106 Progressive Muscular Dystrophy 41 0.042
329
AMR003 Amaurosis Fugax 38 0.042
330
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 38 0.042
331
CYN002 Cyanosis, Transient Neonatal 31 0.042
332
c CRD197 Cardiomyopathy, Hypertrophic, 16 27 0.042
333
c CRD211 Cardiomyopathy, Hypertrophic, 17 23 0.042
334
MNT001 Mantle Cell Lymphoma 70 0.038
335
P CNJ013 Conjunctivitis 65 0.038
336
INC002 Inclusion Body Myositis 63 0.038
337
KRN002 Kearns-Sayre Syndrome 59 0.038
338
P OCL013 Oculodentodigital Dysplasia 59 0.038
339
RHB003 Rhabdomyosarcoma 58 0.038
340
P PRP029 Porphyria 58 0.038
341
P CHN012 Chondrosarcoma 57 0.038
342
P PRM002 Primary Hyperoxaluria 56 0.038
343
HDC001 Headache 54 0.038
344
P THY023 Thymoma 53 0.038
345
P BRC006 Brachydactyly 52 0.038
346
P PLY041 Polymyositis 51 0.038
347
RHM001 Rheumatic Fever 50 0.038
348
P CLL015 Collagen Disease 49 0.038
349
PRP016 Paraplegia 49 0.038
350
PTT009 Pituitary Gland Disease 48 0.038
351
SXL003 Sexual Disorder 47 0.038
352
BRN022 Bronchiectasis 47 0.038
353
HYP085 Hypothalamic Disease 44 0.038
354
PLS016 Plasma Cell Leukemia 42 0.038
355
FML036 Familial Periodic Paralysis 39 0.038
356
SPR035 Superior Vena Cava Syndrome 32 0.038
357
RGH009 Right Atrial Isomerism 32 0.038
358
SBC014 Subclavian Steal Syndrome 29 0.038
359
c ATR061 Atrial Fibrillation, Familial, 10 27 0.038
360
SCN049 Second-Degree Atrioventricular Block 22 0.038
361
c LNR014 Linear Skin Defects with Multiple Congenital Anomalies 3 18 0.038
362
PRP050 Peripheral Arterial Occlusive Disease 1 17 0.038
363
SGM003 Segmentation Syndrome 1 14 0.038
364
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 76 0.034
365
ESP021 Esophageal Cancer 75 0.034
366
MLT021 Multiple System Atrophy 71 0.034
367
MTH009 Mouth Disease 63 0.034
368
P ART023 Arthropathy 63 0.034
369
P ESP024 Esophagitis 62 0.034
370
HTC002 Hutchinson-Gilford Progeria 62 0.034
371
CRB011 Cerebrotendinous Xanthomatosis 60 0.034
372
ETN001 Eating Disorder 60 0.034
373
P CTR002 Cataract 57 0.034
374
ADR005 Adrenal Carcinoma 56 0.034
375
JNT002 Joint Disorders 56 0.034
376
c MYT020 Myotonic Dystrophy 2 55 0.034
377
P INT030 Intracranial Aneurysm 54 0.034
378
CRT049 Critical Limb Ischemia 51 0.034
379
RNL007 Renal Tubular Acidosis 50 0.034
380
P TRN034 Transverse Myelitis 48 0.034
381
MYL001 Myelitis 48 0.034
382
XNT003 Xanthomatosis 47 0.034
383
P ACT150 Acute Adrenal Insufficiency 45 0.034
384
SHH001 Sheehan Syndrome 44 0.034
385
MYC012 Mycetoma 43 0.034
386
IRN002 Iron Metabolism Disease 43 0.034
387
c LNG096 Long Qt Syndrome 15 42 0.034
388
PNM013 Pneumococcal Meningitis 41 0.034
389
MLT008 Multinodular Goiter 41 0.034
390
c SBC007 Subacute Thyroiditis 39 0.034
391
EXT035 Extrinsic Cardiomyopathy 39 0.034
392
P HMF004 Hemifacial Spasm 39 0.034
393
ICH020 Ichthyosis Prematurity Syndrome 37 0.034
394
ADP007 Adie Pupil 34 0.034
395
c PLN021 Peeling Skin Syndrome 3 31 0.034
396
GRN016 Grant Syndrome 30 0.034
397
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 30 0.034
398
THY001 Thyroid Crisis 30 0.034
399
HNS001 Hansen's Disease 29 0.034
400
c ATR038 Atrial Fibrillation, Familial, 3 28 0.034
401
NRG005 Neurogenic Hypertension 27 0.034
402
CCN009 Cocaine Intoxication 20 0.034
403
c BRG010 Brugada Syndrome 8 20 0.034
404
ARL004 Aural Atresia, Congenital 19 0.034
405
WSC001 Wisconsin Syndrome 17 0.034
406
CRT060 Cor Triatriatum Sinister 17 0.034
407
FXP001 Foxp2-Related Speech and Language Disorders 15 0.034
408
ADS006 Aids - Neurological Complications 14 0.034