Search results for "ventricular tachycardia"

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

415 hits were found for 'ventricular tachycardia'

# Family MCID Name MIFTS Score
1
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 56 12.114
2
c VNT013 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1 46 7.442
3
c VNT029 Ventricular Tachycardia, Catecholaminergic Polymorphic, 4 40 6.412
4
c VNT010 Ventricular Tachycardia, Catecholaminergic Polymorphic, 2 25 6.400
5
VNT009 Ventricular Tachycardia, Idiopathic 23 4.898
6
VNT025 Ventricular Tachycardia, Catecholaminergic Polymorphic, 5, with or Without Muscle Weakness 16 3.800
7
c VNT027 Ventricular Tachycardia, Catecholaminergic Polymorphic, 3 11 3.752
8
BDR001 Bidirectional Tachycardia 13 3.412
9
c CLM002 Calm1-Related Catecholaminergic Polymorphic Ventricular Tachycardia 10 3.119
10
INC014 Incessant Infant Ventricular Tachycardia 3 2.216
11
c CSQ001 Casq2-Related Catecholaminergic Polymorphic Ventricular Tachycardia 5 2.188
12
c RYR003 Ryr2-Related Catecholaminergic Polymorphic Ventricular Tachycardia 5 2.188
13
c TRD007 Trdn-Related Catecholaminergic Polymorphic Ventricular Tachycardia 5 2.188
14
c CRD105 Cardiomyopathy, Dilated, 1o 17 2.174
15
c ABC013 Abcc9-Related Dilated Cardiomyopathy 16 2.139
16
P CRD011 Cardiomyopathy 66 0.607
17
P VNT002 Ventricular Septal Defect 59 0.436
18
P MYC007 Myocardial Infarction 80 0.413
19
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 0.395
20
c CNG401 Congenital Heart Disease 67 0.361
21
P HRT032 Heart Disease 64 0.332
22
SNG003 Single Ventricular Heart 23 0.327
23
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 55 0.301
24
P LFT003 Left Ventricular Noncompaction 48 0.297
25
LFT009 Left Ventricular Outflow Tract Obstruction 43 0.296
26
RGH001 Right Bundle Branch Block 43 0.288
27
CNG034 Congestive Heart Failure 72 0.285
28
SYN036 Syncope 45 0.265
29
c CRN172 Coronary Heart Disease 3 19 0.265
30
c CRN175 Coronary Heart Disease 4 19 0.260
31
P HYP061 Hypertrophic Cardiomyopathy 64 0.259
32
P ATR011 Atrial Fibrillation 63 0.257
33
TRN044 Transposition of the Great Arteries 48 0.256
34
TTR001 Tetralogy of Fallot 69 0.255
35
CRD003 Cardiac Sarcoidosis 39 0.251
36
c DLT002 Dilated Cardiomyopathy 75 0.250
37
WLF001 Wolff-Parkinson-White Syndrome 58 0.247
38
ANR040 Aneurysm 56 0.245
39
P CRN178 Coronary Heart Disease 6 22 0.243
40
P BRG001 Brugada Syndrome 59 0.242
41
ATR060 Atrial Standstill, Digenic 51 0.231
42
c ACT075 Acute Myocardial Infarction 61 0.229
43
c CRN174 Coronary Heart Disease 2 19 0.227
44
P LNG028 Long Qt Syndrome 67 0.223
45
ISC004 Ischemia 56 0.218
46
P MYC008 Myocarditis 56 0.217
47
P CRN211 Coronary Artery Disease 74 0.208
48
ISC006 Ischemic Heart Disease 54 0.198
49
c CRN214 Coronary Heart Disease 5 22 0.198
50
ATR057 Atrioventricular Block 49 0.191
51
CRD119 Cardiac Arrest 63 0.190
52
SDD007 Sudden Cardiac Death 46 0.180
53
INF013 Inferior Myocardial Infarction 36 0.177
54
ART111 Artery Disease 56 0.177
55
SYS003 Systolic Heart Failure 42 0.177
56
VNT011 Ventricular Fibrillation, Familial, 1 35 0.172
57
CRD137 Cardiogenic Shock 44 0.172
58
ATN005 Autonomic Dysfunction 44 0.170
59
P PRX010 Paroxysmal Ventricular Fibrillation 33 0.170
60
P ORT004 Orthostatic Intolerance 65 0.161
61
P SCK002 Sick Sinus Syndrome 49 0.157
62
ATN002 Autonomic Nervous System Disease 46 0.155
63
c FML001 Familial Atrial Fibrillation 59 0.154
64
DST006 Diastolic Heart Failure 45 0.153
65
TRC062 Tricuspid Atresia 34 0.153
66
c CLD010 Cold-Induced Sweating Syndrome 1 43 0.147
67
PRP009 Peripartum Cardiomyopathy 41 0.145
68
CNG134 Congenitally Corrected Transposition of the Great Arteries 25 0.143
69
DXT001 Dextrocardia 44 0.142
70
PRN021 Paranasal Sinus Disease 50 0.141
71
NSL022 Nasal Cavity Disease 41 0.141
72
PRP027 Peripheral Vascular Disease 69 0.139
73
PLM033 Pulmonary Embolism 59 0.135
74
P CRD132 Cardiac Conduction Defect 35 0.133
75
P DYS021 Dysautonomia 47 0.133
76
SNT004 Sinoatrial Node Dysfunction and Deafness 25 0.131
77
c CRN176 Coronary Heart Disease 9 19 0.131
78
ADL002 Adult Syndrome 53 0.128
79
ART021 Arteriosclerosis 59 0.124
80
HYP005 Hypokalemia 52 0.124
81
c MYC058 Myocardial Infarction 2 28 0.121
82
HYD012 Hydrops Fetalis 45 0.120
83
ALR002 Al-Raqad Syndrome 36 0.117
84
c HYP595 Hypertension, Essential 69 0.117
85
ART031 Aortic Coarctation 42 0.116
86
P END033 Endocarditis 52 0.116
87
END021 Endomyocardial Fibrosis 47 0.115
88
STS002 Situs Inversus 43 0.114
89
UNV002 Univentricular Heart 24 0.114
90
FNT004 Fainting 33 0.113
91
STR067 Stroke, Ischemic 74 0.113
92
c ACT076 Acute Myocarditis 40 0.113
93
HRT008 Heart Conduction Disease 43 0.112
94
INT007 Intermediate Coronary Syndrome 52 0.111
95
P MSC005 Muscular Dystrophy 64 0.111
96
P MTR012 Mitral Valve Disease 59 0.110
97
c CRN177 Coronary Heart Disease 7 21 0.110
98
CRN030 Coronary Stenosis 50 0.110
99
END074 Endocardium Disease 26 0.108
100
P MYP004 Myopathy 67 0.108
101
GNT019 Giant Cell Myocarditis 31 0.107
102
CHT001 Chaotic Atrial Tachycardia 6 0.107
103
P MSC007 Muscle Hypertrophy 55 0.107
104
HSB001 His Bundle Tachycardia 21 0.107
105
EBS001 Ebstein Anomaly 44 0.106
106
P MYT002 Myotonic Dystrophy 46 0.106
107
PRC013 Pericarditis 52 0.103
108
VND001 Vein Disease 51 0.101
109
P RSP003 Respiratory Failure 68 0.098
110
NXS001 Naxos Disease 46 0.097
111
VSC007 Vascular Disease 51 0.097
112
ART017 Aortic Disease 57 0.097
113
ACR041 Acromelic Frontonasal Dysostosis 45 0.096
114
BRT030 Birth Defects 44 0.096
115
P PHC003 Pheochromocytoma 72 0.096
116
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.094
117
CRB009 Cerebritis 36 0.094
118
KDS001 Kid Syndrome 53 0.093
119
FBR012 Fabry Disease 68 0.093
120
MRF001 Marfan Syndrome 73 0.093
121
c SHR030 Short Qt Syndrome 45 0.093
122
CRT028 Cor Triatriatum 22 0.092
123
END072 Endotheliitis 41 0.092
124
P EPL164 Epilepsy 60 0.091
125
P AMY004 Amyloidosis 63 0.090
126
ANG054 Angina Pectoris 48 0.090
127
CHR066 Chronic Fatigue Syndrome 63 0.089
128
CHL071 Child Syndrome 58 0.089
129
RSP006 Respiratory System Disease 61 0.088
130
P OBS005 Obesity 91 0.088
131
ARR026 Arrhythmogenic Right Ventricular Dysplasia 1 26 0.087
132
CNS002 Constrictive Pericarditis 31 0.087
133
LWN001 Lown-Ganong-Levine Syndrome 28 0.086
134
PCK002 Pick Disease 66 0.086
135
ARR030 Arrhythmogenic Right Ventricular Dysplasia 2 26 0.086
136
END020 Endocardial Fibroelastosis 44 0.084
137
ARR025 Arrhythmogenic Right Ventricular Dysplasia 5 24 0.084
138
c SCK017 Sick Sinus Syndrome 1 32 0.084
139
P THY032 Thyroiditis 57 0.084
140
c MTR002 Mitral Valve Insufficiency 42 0.083
141
P NRP001 Neuropathy 57 0.083
142
CHG001 Chagas Disease 62 0.083
143
STR037 Stress Cardiomyopathy 37 0.082
144
INF034 Infective Endocarditis 50 0.082
145
SNT005 Sinoatrial Node Disease 34 0.081
146
c CRN173 Coronary Heart Disease 8 19 0.081
147
HYP540 Hypertension, Diastolic 40 0.080
148
ESN011 Eisenmenger Syndrome 45 0.080
149
SLP005 Sleep Disorder 52 0.078
150
PTN001 Patent Foramen Ovale 55 0.078
151
CRN017 Coronary Thrombosis 46 0.078
152
P RST002 Restrictive Cardiomyopathy 48 0.077
153
BLD053 Blood Platelet Disease 44 0.077
154
ARR037 Arrhythmogenic Right Ventricular Dysplasia 12 23 0.076
155
MYC005 Myocardial Stunning 44 0.075
156
DCH001 Duchenne Muscular Dystrophy 81 0.074
157
c CRD099 Cardiomyopathy, Dilated, 1e 42 0.073
158
ARR029 Arrhythmogenic Right Ventricular Dysplasia 8 22 0.073
159
BRN106 Burns 52 0.072
160
c BLD124 Bleeding Disorder, Platelet-Type, 11 37 0.071
161
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 27 0.071
162
CRB039 Cerebrovascular Disease 49 0.071
163
MDS022 Mediastinitis 37 0.070
164
ATN004 Autonomic Neuropathy 44 0.070
165
MSC004 Muscle Tissue Disease 35 0.070
166
CHR413 Chronic Myocardial Ischemia 39 0.070
167
ART016 Aortic Aneurysm 67 0.070
168
LPM004 Lipoma 59 0.070
169
P MSC033 Muscle Disorders 52 0.070
170
NRN002 Neuronitis 40 0.070
171
CST001 Costello Syndrome 68 0.069
172
P AST005 Asthma 80 0.069
173
ARR040 Arrhythmogenic Right Ventricular Dysplasia 10 25 0.069
174
CRD001 Cardiac Tamponade 43 0.069
175
P AND016 Andersen Syndrome 57 0.068
176
P ALX003 Alexander Disease 64 0.068
177
c SCK014 Sick Sinus Syndrome 2 27 0.068
178
P HRT035 Heart Block, Congenital 40 0.068
179
HTR003 Heterotaxy 41 0.068
180
FML213 Familial Isolated Arrhythmogenic Ventricular Dysplasia, Right Dominant Form 25 0.068
181
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.067
182
P MNN013 Meningitis 66 0.067
183
ADJ001 Adjustment Disorder 38 0.067
184
P BPL003 Bipolar Disorder 58 0.066
185
P THY054 Thyrotoxic Periodic Paralysis 46 0.066
186
ARR041 Arrhythmogenic Right Ventricular Dysplasia, Familial, 13 19 0.065
187
P RNL015 Renal Hypertension 47 0.065
188
TXC005 Toxic Shock Syndrome 61 0.064
189
WLL006 Wells Syndrome 57 0.064
190
GDS001 Good Syndrome 46 0.064
191
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 41 0.064
192
c LNG044 Long Qt Syndrome 1 59 0.064
193
ANR010 Aneurysm of Sinus of Valsalva 21 0.064
194
FML214 Familial Isolated Arrhythmogenic Ventricular Dysplasia, Biventricular Form 23 0.064
195
FML215 Familial Isolated Arrhythmogenic Ventricular Dysplasia, Left Dominant Form 23 0.064
196
c THR092 Thrombophilia Due to Thrombin Defect 56 0.062
197
HRT007 Heart Cancer 51 0.062
198
P HRT017 Heart Tumor 34 0.062
199
HYP266 Hypoxia 55 0.062
200
c ADL079 Adult Heart Tumor 17 0.062
201
ARR005 Arrhythmogenic Right Ventricular Dysplasia/cardiomyopathy 2 11 0.062
202
ARR008 Arrhythmogenic Right Ventricular Dysplasia/cardiomyopathy 5 11 0.062
203
P SHR029 Short Syndrome 60 0.061
204
P DRM010 Dermatomyositis 59 0.061
205
EXF001 Exfoliation Syndrome 56 0.061
206
LPD004 Lipoid Nephrosis 49 0.061
207
ACR007 Acromegaly 66 0.061
208
PRP080 Peripheral Artery Disease 35 0.061
209
c PST001 Posterior Myocardial Infarction 32 0.061
210
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 57 0.059
211
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 59 0.059
212
P LYM118 Lymphoma 68 0.059
213
P HYP076 Hyperthyroidism 59 0.059
214
PPL022 Papilloma 54 0.059
215
DBL010 Double-Orifice Mitral Valve 16 0.059
216
ARR009 Arrhythmogenic Right Ventricular Dysplasia/cardiomyopathy 6 8 0.059
217
INT084 Intrinsic Cardiomyopathy 34 0.059
218
MLG056 Malignant Hyperthermia 60 0.058
219
LPM005 Lipomatosis 46 0.058
220
P CHR345 Chronic Pain 45 0.058
221
PST055 Postural Hypotension 36 0.058
222
ALN001 Aland Island Eye Disease 45 0.057
223
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 40 0.057
224
CYN002 Cyanosis, Transient Neonatal 29 0.057
225
c SCK022 Sick Sinus Syndrome 3 20 0.057
226
PHY002 Physical Disorder 43 0.057
227
P TBR001 Tuberous Sclerosis 68 0.057
228
CSY001 C Syndrome 49 0.057
229
PRT048 Partial Atrioventricular Canal 30 0.057
230
ATR055 Atrial Septal Aneurysm 23 0.057
231
ARR006 Arrhythmogenic Right Ventricular Dysplasia/cardiomyopathy 3 9 0.057
232
LYM017 Lyme Disease 64 0.055
233
c PND001 Pain Disorder 53 0.055
234
BCK001 Becker Muscular Dystrophy 68 0.055
235
KWS002 Kawasaki Disease 70 0.055
236
CRD180 Cardiomyopathy, Dilated, with Woolly Hair and Keratoderma 37 0.055
237
P ENC018 Encephalopathy 59 0.055
238
P BLD051 Blood Coagulation Disease 44 0.055
239
P PLM064 Pulmonary Sequestration 26 0.055
240
ARR004 Arrhythmogenic Right Ventricular Dysplasia/cardiomyopathy 1 10 0.055
241
ATR024 Atrial Fibrillation and Stroke 19 0.055
242
PRP019 Peripheral Nervous System Disease 52 0.054
243
P PLN008 Peeling Skin Syndrome 45 0.054
244
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 42 0.054
245
HPT074 Hepatic Adenoma, Somatic 35 0.054
246
NWC001 Newcastle Disease 51 0.054
247
c BNG076 Benign Exophthalmos Syndrome 15 0.054
248
c LNG092 Long Qt Syndrome-3 36 0.053
249
ALL026 Allergic Hypersensitivity Disease 53 0.053
250
P MYF003 Myofibrillar Myopathy 39 0.053
251
FCT008 Factitious Disorder 42 0.053
252
VNT031 Ventricular Extrasystoles with Syncope, Perodactyly, and Robin Sequence 14 0.053
253
PLM129 Pulmonary Disease, Chronic Obstructive 61 0.051
254
PRD011 Proud Syndrome 42 0.051
255
NTR041 N-Terminal Acetyltransferase Deficiency 34 0.051
256
CNV002 Conversion Disorder 45 0.051
257
CRN019 Coronary Artery Vasospasm 43 0.051
258
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.050
259
c CRD204 Cardiomyopathy, Hypertrophic, 10 27 0.050
260
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.050
261
P ATX004 Ataxia 53 0.050
262
BRN080 Brain Ischemia 42 0.050
263
MTR027 Mitral Atresia 15 0.050
264
STT001 Status Epilepticus 59 0.050
265
P NRM001 Neuromyelitis Optica 55 0.050
266
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 28 0.050
267
DWN001 Down Syndrome 65 0.048
268
CTS003 Coats Disease 57 0.048
269
NSD001 Nose Disease 51 0.048
270
PRT011 Protein C Deficiency 52 0.048
271
FRS012 First-Degree Atrioventricular Block 29 0.048
272
BLD054 Blood Protein Disease 38 0.048
273
CRB085 Cerebral Hemorrhage 40 0.048
274
BRN071 Brain Injury 51 0.048
275
P MYS003 Myasthenia Gravis 64 0.047
276
CMM005 Common Cold 58 0.047
277
GTR002 Goiter 54 0.047
278
ICH020 Ichthyosis Prematurity Syndrome 38 0.047
279
IRN001 Iron Deficiency Anemia 51 0.047
280
c PLN017 Peeling Skin Syndrome 1 32 0.047
281
ARL004 Aural Atresia, Congenital 22 0.047
282
PRV004 Periventricular Leukomalacia 51 0.047
283
MYX004 Myxedema 36 0.047
284
P HYP071 Hypersensitivity Reaction Type Ii Disease 46 0.047
285
CNT017 Central Nervous System Origin Vertigo 27 0.047
286
HYP017 Hypophosphatemia 43 0.047
287
FXP001 Foxp2-Related Speech and Language Disorders 15 0.047
288
OTP003 Oto-Palatal-Digital Syndrome 14 0.047
289
BCK006 Back Pain 40 0.047
290
LKM006 Leukomalacia 41 0.047
291
BRN105 Burn Scar 36 0.047
292
P FRD001 Friedreich Ataxia 62 0.045
293
BRN028 Brain Cancer 69 0.045
294
MVD001 Moved to 60 0.045
295
P JRV003 Jervell and Lange-Nielsen Syndrome 53 0.045
296
DFC004 Deficiency Anemia 64 0.045
297
CRN041 Carnitine-Acylcarnitine Translocase Deficiency 42 0.045
298
CRD054 Cardiac Arrhythmia, Ankyrin-B-Related 23 0.045
299
HYP066 Hyperglycemia 61 0.045
300
c CRD202 Cardiomyopathy, Hypertrophic, 12 30 0.045
301
c ATR061 Atrial Fibrillation, Familial, 10 29 0.045
302
NSY001 N Syndrome 42 0.045
303
RDN001 Reading Disorder 39 0.045
304
c AST037 Asthma 1 35 0.045
305
PLS016 Plasma Cell Leukemia 52 0.045
306
SPC003 Specific Developmental Disorder 39 0.045
307
LVC002 Levocardia 19 0.045
308
HRT029 Heart Tumor of the Child 16 0.045
309
BRR004 Baroreflex Failure 20 0.045
310
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 77 0.043
311
c SHR033 Short Qt Syndrome 3 26 0.043
312
ATM052 Autoimmune Disease 1 26 0.043
313
UND005 Undifferentiated Pleomorphic Sarcoma 39 0.043
314
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 34 0.043
315
ATM013 Autoimmune Disease of Cardiovascular System 14 0.043
316
DGT004 Digitalis Poisoning 11 0.043
317
P BRS047 Breast Cancer 100 0.042
318
ANX002 Anxiety Disorder 67 0.042
319
GST050 Gastrointestinal System Disease 58 0.042
320
P NRV007 Nervous System Disease 71 0.042
321
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 40 0.042
322
NTR005 Nutritional Deficiency Disease 51 0.042
323
P LKM002 Leukemia 70 0.042
324
P PRP029 Porphyria 56 0.042
325
P MYS005 Myositis 57 0.042
326
PLN006 Poland Syndrome 48 0.042
327
QDR001 Quadriplegia 51 0.042
328
c CRD197 Cardiomyopathy, Hypertrophic, 16 24 0.042
329
c CRD211 Cardiomyopathy, Hypertrophic, 17 21 0.042
330
MVM001 Movement Disease 45 0.042
331
NRM005 Neuromuscular Disease 56 0.042
332
CRC006 Carcinoid Syndrome 51 0.042
333
AMR003 Amaurosis Fugax 38 0.042
334
P BRC006 Brachydactyly 53 0.042
335
GNR004 Generalized Anxiety Disorder 49 0.042
336
P LMY004 Leiomyosarcoma 54 0.042
337
HMN009 Hemangioblastoma 45 0.042
338
PHC013 Phaeochromocytoma 47 0.042
339
P EXN002 Exanthem 57 0.042
340
c FML191 Familial Long Qt Syndrome 39 0.042
341
FBR054 Fibroma 44 0.042
342
TRM010 Traumatic Brain Injury 52 0.042
343
LMB062 Limb Ischemia 48 0.042
344
INC002 Inclusion Body Myositis 64 0.038
345
KRN002 Kearns-Sayre Syndrome 60 0.038
346
P OCL013 Oculodentodigital Dysplasia 58 0.038
347
P CNJ013 Conjunctivitis 65 0.038
348
MTH009 Mouth Disease 63 0.038
349
BRN022 Bronchiectasis 55 0.038
350
P CHN012 Chondrosarcoma 57 0.038
351
P PRM002 Primary Hyperoxaluria 54 0.038
352
RHM027 Rheumatic Disease 55 0.038
353
RHB003 Rhabdomyosarcoma 55 0.038
354
PRP016 Paraplegia 49 0.038
355
PTT009 Pituitary Gland Disease 45 0.038
356
CND002 Conduct Disorder 54 0.038
357
RGH009 Right Atrial Isomerism 31 0.038
358
LRN003 Learning Disability 49 0.038
359
FML036 Familial Periodic Paralysis 39 0.038
360
P CLL015 Collagen Disease 49 0.038
361
SPR035 Superior Vena Cava Syndrome 31 0.038
362
HDC001 Headache 52 0.038
363
c LNR014 Linear Skin Defects with Multiple Congenital Anomalies 3 16 0.038
364
HYP085 Hypothalamic Disease 43 0.038
365
SXL003 Sexual Disorder 45 0.038
366
SBC014 Subclavian Steal Syndrome 30 0.038
367
P THY023 Thymoma 57 0.038
368
P PLY041 Polymyositis 49 0.038
369
SCN049 Second-Degree Atrioventricular Block 22 0.038
370
HNS001 Hansen's Disease 30 0.038
371
PRP050 Peripheral Arterial Occlusive Disease 1 16 0.038
372
SGM003 Segmentation Syndrome 1 13 0.038
373
c PRG106 Progressive Muscular Dystrophy 40 0.038
374
ESP021 Esophageal Cancer 75 0.034
375
c MYT020 Myotonic Dystrophy 2 56 0.034
376
CRB011 Cerebrotendinous Xanthomatosis 60 0.034
377
MLT021 Multiple System Atrophy 71 0.034
378
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 32 0.034
379
P ART023 Arthropathy 63 0.034
380
ADR005 Adrenal Carcinoma 57 0.034
381
C3D001 C3 Deficiency 50 0.034
382
ETN001 Eating Disorder 59 0.034
383
c ATR038 Atrial Fibrillation, Familial, 3 27 0.034
384
GRN016 Grant Syndrome 30 0.034
385
RNL007 Renal Tubular Acidosis 50 0.034
386
P ESP024 Esophagitis 62 0.034
387
DBT001 Diabetic Ketoacidosis 45 0.034
388
c BRG010 Brugada Syndrome 8 18 0.034
389
c PLN021 Peeling Skin Syndrome 3 30 0.034
390
c LNG096 Long Qt Syndrome 15 42 0.034
391
HTC002 Hutchinson-Gilford Progeria 51 0.034
392
SHH001 Sheehan Syndrome 42 0.034
393
SKN023 Skin Tag 48 0.034
394
P CTR002 Cataract 57 0.034
395
P PRG013 Paraganglioma 54 0.034
396
P INT030 Intracranial Aneurysm 52 0.034
397
IRN002 Iron Metabolism Disease 38 0.034
398
MYC012 Mycetoma 44 0.034
399
XNT003 Xanthomatosis 45 0.034
400
c SBC007 Subacute Thyroiditis 42 0.034
401
THY001 Thyroid Crisis 29 0.034
402
JNT002 Joint Disorders 55 0.034
403
P ACT150 Acute Adrenal Insufficiency 36 0.034
404
CRT060 Cor Triatriatum Sinister 19 0.034
405
RHM007 Rheumatic Congestive Heart Failure 22 0.034
406
P TRN034 Transverse Myelitis 43 0.034
407
MYL001 Myelitis 35 0.034
408
MLT008 Multinodular Goiter 40 0.034
409
PNM013 Pneumococcal Meningitis 41 0.034
410
EXT035 Extrinsic Cardiomyopathy 38 0.034
411
CCN009 Cocaine Intoxication 18 0.034
412
P HMF004 Hemifacial Spasm 38 0.034
413
WSC001 Wisconsin Syndrome 16 0.034
414
ADS006 Aids - Neurological Complications 12 0.034
415
NRG005 Neurogenic Hypertension 25 0.034