Search results for ventricular tachycardia

410 hits were found for ventricular tachycardia

# Family MCID Name MIFTS Score
1
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 61 12.497
2
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 47 10.146
3
c VNT010 Ventricular Tachycardia, Catecholaminergic Polymorphic, 2 30 8.901
4
c VNT029 Ventricular Tachycardia, Catecholaminergic Polymorphic, 4 30 8.612
5
VNT032 Ventricular Tachycardia, Familial 26 6.835
6
c VNT027 Ventricular Tachycardia, Catecholaminergic Polymorphic, 3 21 6.033
7
VNT025 Ventricular Tachycardia, Catecholaminergic Polymorphic, 5, with or Without Muscle Weakness 13 4.555
8
c CRD105 Cardiomyopathy, Dilated, 1o 36 3.913
9
BDR001 Bidirectional Tachycardia 12 3.533
10
INC014 Incessant Infant Ventricular Tachycardia 3 3.228
11
c CTC003 Catecholaminergic Polymorphic Ventricular Tachycardia 5 7 2.329
12
P HRT032 Heart Disease 80 0.524
13
P VNT002 Ventricular Septal Defect 59 0.468
14
P MYC007 Myocardial Infarction 81 0.436
15
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 57 0.336
16
P LFT003 Left Ventricular Noncompaction 52 0.320
17
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 54 0.308
18
c PRG042 Progressive Familial Heart Block, Type Ia 57 0.308
19
CNG034 Congestive Heart Failure 74 0.305
20
RGH001 Right Bundle Branch Block 44 0.299
21
c PRG043 Progressive Familial Heart Block, Type Ib 40 0.296
22
TRN044 Transposition of the Great Arteries 49 0.277
23
P TTR001 Tetralogy of Fallot 70 0.277
24
P ATR011 Atrial Fibrillation 68 0.272
25
P HYP061 Hypertrophic Cardiomyopathy 65 0.271
26
CRD003 Cardiac Sarcoidosis 40 0.267
27
ISC004 Ischemia 66 0.263
28
ANR040 Aneurysm 61 0.262
29
SYN036 Syncope 46 0.258
30
WLF001 Wolff-Parkinson-White Syndrome 57 0.255
31
P DLT002 Dilated Cardiomyopathy 76 0.252
32
P ORT004 Orthostatic Intolerance 68 0.247
33
P BRG001 Brugada Syndrome 61 0.246
34
ISC006 Ischemic Heart Disease 73 0.245
35
P CRN018 Coronary Artery Anomaly 69 0.240
36
c ACT075 Acute Myocardial Infarction 64 0.237
37
P MYC008 Myocarditis 58 0.228
38
P LNG028 Long Qt Syndrome 63 0.228
39
ATR057 Atrioventricular Block 52 0.208
40
P CRN300 Coronary Heart Disease 1 57 0.206
41
ART140 Arteries, Anomalies of 51 0.185
42
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.184
43
CRD119 Cardiac Arrest 63 0.184
44
P CRD132 Cardiac Conduction Defect 53 0.180
45
P PLM037 Pulmonary Hypertension 79 0.178
46
INF013 Inferior Myocardial Infarction 36 0.175
47
DBL004 Double Discordia 19 0.174
48
CRD137 Cardiogenic Shock 45 0.174
49
ATN005 Autonomic Dysfunction 51 0.170
50
CRD223 Cardiac Arrhythmia 52 0.169
51
c BLD140 Blood Group, I System 37 0.169
52
CNT061 Conotruncal Heart Malformations 70 0.161
53
P SCK002 Sick Sinus Syndrome 53 0.161
54
AGN016 Aging 65 0.158
55
CNG134 Congenitally Corrected Transposition of the Great Arteries 28 0.156
56
c ATR087 Atrial Standstill 1 59 0.156
57
TRC062 Tricuspid Atresia 47 0.155
58
c HYP595 Hypertension, Essential 78 0.154
59
PRP009 Peripartum Cardiomyopathy 53 0.154
60
P PRX010 Paroxysmal Ventricular Fibrillation 28 0.153
61
DXT001 Dextrocardia 55 0.148
62
PLM033 Pulmonary Embolism 62 0.146
63
P ANR048 Aniridia 1 68 0.145
64
ANR038 Anorexia Nervosa 1 21 0.144
65
BLD137 Blood Group--Ahonen 17 0.144
66
SYS003 Systolic Heart Failure 44 0.143
67
VSC007 Vascular Disease 71 0.138
68
P DYS021 Dysautonomia 47 0.137
69
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 59 0.136
70
CHT001 Chaotic Atrial Tachycardia 12 0.135
71
NXS001 Naxos Disease 47 0.130
72
PRC013 Pericarditis 55 0.130
73
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.130
74
P ART021 Arteriosclerosis 62 0.129
75
END021 Endomyocardial Fibrosis 51 0.129
76
THR024 Thrombosis 61 0.128
77
HYP005 Hypokalemia 53 0.127
78
DST006 Diastolic Heart Failure 47 0.123
79
c ACT076 Acute Myocarditis 48 0.120
80
STS002 Situs Inversus 48 0.120
81
P END033 Endocarditis 58 0.118
82
HYD012 Hydrops Fetalis 50 0.118
83
HYD059 Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect 34 0.118
84
ARR046 Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 38 0.117
85
P MYT002 Myotonic Dystrophy 50 0.116
86
P MSC005 Muscular Dystrophy 66 0.114
87
P MTR012 Mitral Valve Disease 59 0.111
88
ART031 Aortic Coarctation 48 0.111
89
GNT019 Giant Cell Myocarditis 34 0.111
90
HSB001 His Bundle Tachycardia 23 0.109
91
UNV002 Univentricular Heart 29 0.108
92
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.107
93
FNT004 Fainting 36 0.106
94
P ATR001 Atrioventricular Septal Defect 56 0.105
95
EBS001 Ebstein Anomaly 52 0.105
96
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.104
97
P PHC003 Pheochromocytoma 72 0.102
98
P ATR010 Atrial Heart Septal Defect 45 0.101
99
LNG099 Lung Disease 67 0.100
100
HPT082 Hepatic Adenomas, Familial 52 0.099
101
CRN030 Coronary Stenosis 52 0.099
102
CNS002 Constrictive Pericarditis 37 0.098
103
CRT028 Cor Triatriatum 25 0.096
104
FBR012 Fabry Disease 72 0.096
105
CRB009 Cerebritis 41 0.095
106
END072 Endotheliitis 46 0.095
107
c SHR030 Short Qt Syndrome 42 0.095
108
ARR045 Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 38 0.095
109
CHG001 Chagas Disease 72 0.094
110
ARR018 Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 42 0.094
111
P AMY004 Amyloidosis 69 0.093
112
ANG054 Angina Pectoris 53 0.093
113
P NRP001 Neuropathy 63 0.092
114
c CRD099 Cardiomyopathy, Dilated, 1e 53 0.091
115
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.090
116
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.090
117
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.090
118
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.090
119
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.090
120
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.090
121
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.090
122
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.090
123
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.090
124
ARR050 Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 35 0.089
125
c MTR002 Mitral Valve Insufficiency 46 0.089
126
END020 Endocardial Fibroelastosis 46 0.089
127
MRF001 Marfan Syndrome 75 0.088
128
P THY032 Thyroiditis 56 0.088
129
P MYP004 Myopathy 69 0.088
130
c GRV008 Graves Disease 1 52 0.087
131
ALR002 Al-Raqad Syndrome 30 0.087
132
CHR066 Chronic Fatigue Syndrome 67 0.085
133
ESN011 Eisenmenger Syndrome 49 0.084
134
ARR041 Arrhythmogenic Right Ventricular Dysplasia, Familial, 13 18 0.083
135
INF034 Infective Endocarditis 56 0.083
136
c CRD087 Cardiomyopathy, Familial Hypertrophic, 10 22 0.082
137
ATR048 Atrial Tachyarrhythmia with Short Pr Interval 34 0.082
138
P RST002 Restrictive Cardiomyopathy 51 0.080
139
P EPL164 Epilepsy 70 0.080
140
PTN001 Patent Foramen Ovale 58 0.080
141
P THL005 Thalassemia 65 0.079
142
ARR028 Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 19 0.079
143
AST005 Asthma 83 0.079
144
SLP005 Sleep Disorder 59 0.079
145
CRD180 Cardiomyopathy, Dilated, with Woolly Hair and Keratoderma 41 0.079
146
CRD237 Cardiomyopathy, Dilated, 1aa, with or Without Left Ventricular Noncompaction 22 0.079
147
MYC005 Myocardial Stunning 47 0.078
148
ARR024 Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 19 0.078
149
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.078
150
PPL022 Papilloma 58 0.077
151
CST001 Costello Syndrome 67 0.077
152
P ENC018 Encephalopathy 58 0.075
153
HRT038 Heart, Malformation of 22 0.075
154
ANX010 Anxiety 72 0.075
155
MSC157 Muscular Dystrophy, Duchenne Type 74 0.074
156
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.074
157
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.074
158
ATN004 Autonomic Neuropathy 46 0.072
159
BRN106 Burns 57 0.072
160
ALP046 Alport Syndrome, X-Linked 74 0.071
161
P RSP003 Respiratory Failure 71 0.071
162
c LNG048 Long Qt Syndrome 3 46 0.071
163
HYP266 Hypoxia 61 0.071
164
MDS022 Mediastinitis 44 0.071
165
P LYM118 Lymphoma 71 0.070
166
CRB039 Cerebrovascular Disease 68 0.070
167
c CNT035 Central Nervous System Disease 65 0.070
168
c LPM012 Lipomatosis, Multiple 64 0.070
169
c LNG044 Long Qt Syndrome 1 61 0.070
170
P HYP076 Hyperthyroidism 56 0.070
171
P THY054 Thyrotoxic Periodic Paralysis 54 0.070
172
NRN002 Neuronitis 43 0.070
173
HRT008 Heart Conduction Disease 32 0.070
174
OGD001 Ogden Syndrome 35 0.070
175
P MNN013 Meningitis 71 0.070
176
CRD001 Cardiac Tamponade 45 0.070
177
FML213 Familial Isolated Arrhythmogenic Ventricular Dysplasia, Right Dominant Form 26 0.070
178
c LNG057 Long Qt Syndrome 13 39 0.069
179
c MYT021 Myotonic Dystrophy 1 68 0.069
180
TMT001 Timothy Syndrome 52 0.069
181
c LNG050 Long Qt Syndrome 5 43 0.069
182
INT084 Intrinsic Cardiomyopathy 29 0.069
183
c GLY009 Glycogen Storage Disease Xv 26 0.069
184
PLC008 Placenta Disease 48 0.068
185
P DRM010 Dermatomyositis 65 0.067
186
CRN041 Carnitine-Acylcarnitine Translocase Deficiency 44 0.067
187
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 39 0.067
188
SPN331 Spondyloocular Syndrome 34 0.067
189
HTR003 Heterotaxy 46 0.067
190
c LNG051 Long Qt Syndrome 6 42 0.067
191
THR099 Third-Degree Atrioventricular Block 37 0.066
192
FML214 Familial Isolated Arrhythmogenic Ventricular Dysplasia, Biventricular Form 25 0.066
193
FML215 Familial Isolated Arrhythmogenic Ventricular Dysplasia, Left Dominant Form 25 0.066
194
ATR089 Atrioventricular Dissociation 17 0.065
195
c LNG047 Long Qt Syndrome 2 49 0.065
196
RST023 Resting Heart Rate, Variation in 42 0.065
197
c LNG056 Long Qt Syndrome 12 36 0.065
198
CYN002 Cyanosis, Transient Neonatal 32 0.065
199
P JRV004 Jervell and Lange-Nielsen Syndrome 1 54 0.064
200
c SCK017 Sick Sinus Syndrome 1 23 0.064
201
ANR010 Aneurysm of Sinus of Valsalva 29 0.062
202
VNT031 Ventricular Extrasystoles with Syncope, Perodactyly, and Robin Sequence 17 0.062
203
c FML191 Familial Long Qt Syndrome 43 0.061
204
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 35 0.061
205
ACR007 Acromegaly 70 0.061
206
c CRD093 Cardiomyopathy, Dilated, 1a 58 0.061
207
P MLT020 Multiple Sclerosis 85 0.060
208
ART016 Aortic Aneurysm 70 0.060
209
P MLG056 Malignant Hyperthermia 60 0.060
210
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 41 0.060
211
c LNG053 Long Qt Syndrome 9 40 0.060
212
c FML294 Familial Short Qt Syndrome 34 0.060
213
c SCK014 Sick Sinus Syndrome 2 22 0.060
214
c CRD238 Cardiomyopathy, Familial Hypertrophic, 17 20 0.060
215
P RNL015 Renal Hypertension 46 0.060
216
DBL010 Double-Orifice Mitral Valve 17 0.060
217
PST055 Postural Hypotension 40 0.058
218
ARL004 Aural Atresia, Congenital 27 0.058
219
P NRV007 Nervous System Disease 75 0.058
220
KWS002 Kawasaki Disease 72 0.058
221
SDD001 Sudden Infant Death Syndrome 61 0.057
222
P MYP006 Myopia 56 0.057
223
c CRD148 Cardiomyopathy, Familial Hypertrophic, 16 19 0.057
224
STR067 Stroke, Ischemic 84 0.056
225
PRP027 Peripheral Vascular Disease 71 0.056
226
BRN056 Bronchopulmonary Dysplasia 61 0.056
227
CRN017 Coronary Thrombosis 48 0.056
228
HTR014 Heterotaxy, Visceral, 1, X-Linked 39 0.056
229
ATR055 Atrial Septal Aneurysm 27 0.056
230
P PLM064 Pulmonary Sequestration 25 0.056
231
VNT005 Ventricular Extrasystoles with Syncopal Episodes - Perodactyly - Robin Sequence 7 0.056
232
P NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 57 0.055
233
P SRC025 Sarcoidosis 1 63 0.055
234
c FML001 Familial Atrial Fibrillation 55 0.055
235
IRN002 Iron Metabolism Disease 45 0.055
236
CNT009 Central Core Myopathy 31 0.055
237
SCN049 Second-Degree Atrioventricular Block 29 0.055
238
c LNG098 Long Qt Syndrome 14 26 0.055
239
c LNR014 Linear Skin Defects with Multiple Congenital Anomalies 3 21 0.055
240
c ATR061 Atrial Fibrillation, Familial, 10 18 0.055
241
FBR023 Fibrinogen Deficiency, Congenital 18 0.055
242
STT001 Status Epilepticus 60 0.054
243
MSC152 Muscular Dystrophy, Becker Type 64 0.053
244
BRR014 Barrett Esophagus 64 0.053
245
P MYF003 Myofibrillar Myopathy 44 0.053
246
MNT002 Mental Depression 60 0.051
247
IRN001 Iron Deficiency Anemia 55 0.051
248
PRV004 Periventricular Leukomalacia 53 0.051
249
P LPM005 Lipomatosis 50 0.051
250
LKM006 Leukomalacia 46 0.051
251
FML036 Familial Periodic Paralysis 41 0.051
252
HRS016 Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction 20 0.051
253
c CRD081 Cardiomyopathy, Familial Hypertrophic, 12 19 0.051
254
P TBR001 Tuberous Sclerosis 69 0.051
255
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 51 0.051
256
CRN019 Coronary Artery Vasospasm 42 0.051
257
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.051
258
LYM017 Lyme Disease 68 0.050
259
P SCH015 Schizophrenia 71 0.048
260
HYP066 Hyperglycemia 64 0.048
261
BRN071 Brain Injury 54 0.048
262
c RBN009 Robinow Syndrome, Autosomal Recessive 42 0.048
263
FRS012 First-Degree Atrioventricular Block 33 0.048
264
ANT005 Anteroseptal Myocardial Infarction 24 0.048
265
BDY007 Body Mass Index Quantitative Trait Locus 1 23 0.048
266
MTR027 Mitral Atresia 16 0.048
267
P MYS003 Myasthenia Gravis 73 0.048
268
HTC003 Hutchinson-Gilford Progeria Syndrome 62 0.048
269
P HYP370 Hypokalemic Periodic Paralysis, Type 1 59 0.048
270
HDC001 Headache 55 0.048
271
GTR002 Goiter 53 0.048
272
ENC010 Encephalocraniocutaneous Lipomatosis 48 0.048
273
HYP017 Hypophosphatemia 45 0.048
274
MYX004 Myxedema 44 0.048
275
c LPD035 Lipodystrophy, Congenital Generalized, Type 4 36 0.048
276
c MYS011 Myasthenia Gravis Congenital 28 0.048
277
P BRS047 Breast Cancer 100 0.046
278
P LKM002 Leukemia 75 0.046
279
BRC012 Brucellosis 71 0.046
280
ATM095 Autoimmune Disease 66 0.046
281
GST050 Gastrointestinal System Disease 66 0.046
282
NRM005 Neuromuscular Disease 60 0.046
283
CRC006 Carcinoid Syndrome 59 0.046
284
P INT030 Intracranial Aneurysm 58 0.046
285
P FRD012 Friedreich Ataxia 1 58 0.046
286
c MCL062 Mucolipidosis Ii Alpha/beta 58 0.046
287
THR100 Thrombocytopenic Purpura, Autoimmune 57 0.046
288
P PLY041 Polymyositis 57 0.046
289
MSC033 Muscle Disorders 53 0.046
290
RGH009 Right Atrial Isomerism 48 0.046
291
c LNG096 Long Qt Syndrome 15 38 0.046
292
LNG054 Lung Agenesis 34 0.046
293
CRD054 Cardiac Arrhythmia, Ankyrin-B-Related 24 0.046
294
LVC002 Levocardia 20 0.046
295
P NRM001 Neuromyelitis Optica 67 0.043
296
CMM005 Common Cold 62 0.043
297
IMM136 Immune System Disease 57 0.043
298
c MYT020 Myotonic Dystrophy 2 56 0.043
299
TTL012 Total Anomalous Pulmonary Venous Return 1 42 0.043
300
DGT004 Digitalis Poisoning 12 0.043
301
BRN028 Brain Cancer 72 0.042
302
P MYS005 Myositis 63 0.042
303
RHM027 Rheumatic Disease 62 0.042
304
P EXN002 Exanthem 62 0.042
305
RHM001 Rheumatic Fever 59 0.042
306
P LMY004 Leiomyosarcoma 59 0.042
307
CNT105 Central Core Disease of Muscle 57 0.042
308
HMN009 Hemangioblastoma 56 0.042
309
TRM010 Traumatic Brain Injury 54 0.042
310
QDR001 Quadriplegia 54 0.042
311
P CLL015 Collagen Disease 53 0.042
312
PHC013 Phaeochromocytoma 44 0.042
313
MSC004 Muscle Tissue Disease 39 0.042
314
c CRD104 Cardiomyopathy, Dilated, 1p 38 0.042
315
AMR003 Amaurosis Fugax 37 0.042
316
c MTR080 Mitral Valve Prolapse 1 34 0.042
317
RHM035 Rheumatic Fever-Related Antigen 34 0.042
318
PRT048 Partial Atrioventricular Canal 32 0.042
319
P RNG031 Ring Chromosome Y Syndrome 29 0.042
320
CRD231 Cardiomyopathy, Infantile Histiocytoid 27 0.042
321
P ART023 Arthropathy 68 0.039
322
P CNJ013 Conjunctivitis 67 0.039
323
P THY023 Thymoma 65 0.039
324
INC002 Inclusion Body Myositis 64 0.039
325
RCK004 Rickets 63 0.039
326
P PRP029 Porphyria 62 0.039
327
c THR092 Thrombophilia Due to Thrombin Defect 61 0.039
328
P RHB003 Rhabdomyosarcoma 61 0.039
329
JNT002 Joint Disorders 60 0.039
330
KRN002 Kearns-Sayre Syndrome 59 0.039
331
P OCL013 Oculodentodigital Dysplasia 57 0.039
332
P BRC006 Brachydactyly 57 0.039
333
PTT009 Pituitary Gland Disease 56 0.039
334
P CHN012 Chondrosarcoma 56 0.039
335
BRN022 Bronchiectasis 55 0.039
336
INT007 Intermediate Coronary Syndrome 55 0.039
337
P PRM002 Primary Hyperoxaluria 53 0.039
338
PRP016 Paraplegia 53 0.039
339
PNC001 Pancytopenia 50 0.039
340
AYM001 Ayme-Gripp Syndrome 40 0.039
341
INT052 Intestinal Volvulus 38 0.039
342
ENT004 Enthesopathy 38 0.039
343
c THY107 Thymoma, Familial 34 0.039
344
SBC014 Subclavian Steal Syndrome 31 0.039
345
ATX010 Ataxia Neuropathy Spectrum 29 0.039
346
CCN009 Cocaine Intoxication 22 0.039
347
BRR004 Baroreflex Failure 21 0.039
348
CRD240 Cardiomyopathy, Dilated, with Woolly Hair, Keratoderma, and Tooth Agenesis 19 0.039
349
MTR030 Mitral Valve Prolapse, Familial, X-Linked 16 0.039
350
ESP021 Esophageal Cancer 79 0.034
351
MNT001 Mantle Cell Lymphoma 76 0.034
352
WGN006 Wegener Granulomatosis 71 0.034
353
P ESP024 Esophagitis 64 0.034
354
CRB011 Cerebrotendinous Xanthomatosis 64 0.034
355
P CTR002 Cataract 60 0.034
356
UND005 Undifferentiated Pleomorphic Sarcoma 59 0.034
357
ADR005 Adrenal Carcinoma 59 0.034
358
P PRG013 Paraganglioma 57 0.034
359
PRR016 Pierre Robin Syndrome 57 0.034
360
c ANM038 Anemia, Autoimmune Hemolytic 56 0.034
361
CHL028 Childhood Type Dermatomyositis 55 0.034
362
CND002 Conduct Disorder 54 0.034
363
XNT003 Xanthomatosis 53 0.034
364
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.034
365
P TRN034 Transverse Myelitis 53 0.034
366
c BLM008 Bulimia Nervosa 2 53 0.034
367
c ACT134 Acute Liver Failure 52 0.034
368
P FNC043 Fanconi Anemia, Complementation Group E 52 0.034
369
MYL001 Myelitis 52 0.034
370
P RNL007 Renal Tubular Acidosis 51 0.034
371
P ACT150 Acute Adrenal Insufficiency 51 0.034
372
TRS021 Triosephosphate Isomerase Deficiency 51 0.034
373
P OTT001 Otitis Externa 51 0.034
374
SHH001 Sheehan Syndrome 50 0.034
375
SPR010 Sporotrichosis 50 0.034
376
DBT084 Diabetes Mellitus, Ketosis-Prone 50 0.034
377
P MYP087 Myopathy, Tubular Aggregate, 1 48 0.034
378
P PRM001 Primary Cutaneous Amyloidosis 48 0.034
379
c LBR012 Leber Congenital Amaurosis 2 47 0.034
380
DYS073 Dysphagia 47 0.034
381
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 47 0.034
382
MYC012 Mycetoma 46 0.034
383
P MLT008 Multinodular Goiter 44 0.034
384
PLS016 Plasma Cell Leukemia 43 0.034
385
c SBC007 Subacute Thyroiditis 43 0.034
386
c DFN190 Deafness, Autosomal Dominant 2a 42 0.034
387
BRD001 Brody Myopathy 41 0.034
388
P HMF004 Hemifacial Spasm 41 0.034
389
PNG002 Pain Agnosia 41 0.034
390
PNM013 Pneumococcal Meningitis 40 0.034
391
c DYS146 Dystonia 24 40 0.034
392
PRM237 Primary Hypomagnesemia 40 0.034
393
P CLR001 Clear Cell Acanthoma 40 0.034
394
c DFN174 Deafness, Autosomal Recessive 44 40 0.034
395
OTM001 Otomycosis 39 0.034
396
ICH020 Ichthyosis Prematurity Syndrome 39 0.034
397
c ACT037 Acute Dacryocystitis 36 0.034
398
ASC009 Ascites, Chylous 35 0.034
399
c INF145 Infantile Liver Failure Syndrome 1 33 0.034
400
SPN033 Spontaneous Ocular Nystagmus 33 0.034
401
EXT056 External Ear Disease 31 0.034
402
PRM026 Primary Systemic Mycosis 31 0.034
403
THY001 Thyroid Crisis 30 0.034
404
RCH002 Richards-Rundle Syndrome 30 0.034
405
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 27 0.034
406
CRT060 Cor Triatriatum Sinister 21 0.034
407
c SHR033 Short Qt Syndrome 3 19 0.034
408
c BRG010 Brugada Syndrome 8 16 0.034
409
c ATR038 Atrial Fibrillation, Familial, 3 16 0.034
410
EMR021 Emery-Dreifuss Syndrome 9 0.034
Content
Loading form....