Search results for "ventricular tachycardia"

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

518 hits were found for 'ventricular tachycardia'

# Family MCID Name MIFTS Score
1
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 60 12.276
2
c VNT013 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1 49 8.572
3
c VNT029 Ventricular Tachycardia, Catecholaminergic Polymorphic, 4 41 7.985
4
c VNT010 Ventricular Tachycardia, Catecholaminergic Polymorphic, 2 37 7.697
5
c VNT027 Ventricular Tachycardia, Catecholaminergic Polymorphic, 3 20 5.659
6
VNT009 Ventricular Tachycardia, Idiopathic 16 4.799
7
VNT025 Ventricular Tachycardia, Catecholaminergic Polymorphic, 5, with or Without Muscle Weakness 15 4.288
8
BDR001 Bidirectional Tachycardia 13 3.295
9
c CLM002 Calm1-Related Catecholaminergic Polymorphic Ventricular Tachycardia 11 3.044
10
INC014 Incessant Infant Ventricular Tachycardia 3 3.040
11
c CRD105 Cardiomyopathy, Dilated, 1o 37 3.009
12
c CTC003 Catecholaminergic Polymorphic Ventricular Tachycardia 5 8 2.189
13
c CSQ001 Casq2-Related Catecholaminergic Polymorphic Ventricular Tachycardia 6 2.153
14
c RYR003 Ryr2-Related Catecholaminergic Polymorphic Ventricular Tachycardia 6 2.153
15
c TRD007 Trdn-Related Catecholaminergic Polymorphic Ventricular Tachycardia 6 2.153
16
c ABC013 Abcc9-Related Dilated Cardiomyopathy 11 2.110
17
P CRD011 Cardiomyopathy 68 0.573
18
P VNT002 Ventricular Septal Defect 60 0.429
19
P HRT032 Heart Disease 75 0.396
20
P MYC007 Myocardial Infarction 79 0.390
21
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.361
22
SNG003 Single Ventricular Heart 22 0.306
23
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 56 0.290
24
LFT009 Left Ventricular Outflow Tract Obstruction 43 0.290
25
P LFT003 Left Ventricular Noncompaction 50 0.280
26
CNG034 Congestive Heart Failure 72 0.274
27
RGH001 Right Bundle Branch Block 44 0.254
28
TRN044 Transposition of the Great Arteries 48 0.246
29
TTR001 Tetralogy of Fallot 71 0.240
30
P ATR011 Atrial Fibrillation 66 0.232
31
c CRN175 Coronary Heart Disease 4 19 0.228
32
ANR040 Aneurysm 57 0.228
33
c DLT002 Dilated Cardiomyopathy 76 0.226
34
c CRN172 Coronary Heart Disease 3 19 0.225
35
P CRN178 Coronary Heart Disease 6 21 0.225
36
CRD003 Cardiac Sarcoidosis 42 0.225
37
ATR060 Atrial Standstill, Digenic 51 0.220
38
SYN036 Syncope 47 0.219
39
c ACT075 Acute Myocardial Infarction 60 0.219
40
WLF001 Wolff-Parkinson-White Syndrome 56 0.214
41
P BRG001 Brugada Syndrome 59 0.212
42
ISC004 Ischemia 61 0.204
43
P MYC008 Myocarditis 54 0.197
44
P LNG028 Long Qt Syndrome 64 0.189
45
P CRN211 Coronary Artery Disease 74 0.187
46
c CRN214 Coronary Heart Disease 5 22 0.185
47
ISC006 Ischemic Heart Disease 68 0.184
48
c CRN174 Coronary Heart Disease 2 20 0.183
49
ATR057 Atrioventricular Block 49 0.176
50
SYS003 Systolic Heart Failure 43 0.170
51
P PLM037 Pulmonary Hypertension 79 0.167
52
INF013 Inferior Myocardial Infarction 35 0.164
53
VNT011 Ventricular Fibrillation, Familial, 1 41 0.160
54
SDD007 Sudden Cardiac Death 47 0.159
55
ART111 Artery Disease 55 0.157
56
CRD137 Cardiogenic Shock 46 0.156
57
CRD119 Cardiac Arrest 61 0.153
58
DST006 Diastolic Heart Failure 46 0.148
59
ATN005 Autonomic Dysfunction 49 0.148
60
P PRX010 Paroxysmal Ventricular Fibrillation 37 0.143
61
P SCK002 Sick Sinus Syndrome 50 0.142
62
c FML001 Familial Atrial Fibrillation 58 0.140
63
TRC062 Tricuspid Atresia 43 0.138
64
CNG134 Congenitally Corrected Transposition of the Great Arteries 24 0.135
65
P ORT004 Orthostatic Intolerance 64 0.133
66
PRP009 Peripartum Cardiomyopathy 42 0.132
67
ATN002 Autonomic Nervous System Disease 48 0.132
68
DXT001 Dextrocardia 43 0.128
69
PRN021 Paranasal Sinus Disease 49 0.128
70
NSL022 Nasal Cavity Disease 38 0.128
71
PRP027 Peripheral Vascular Disease 69 0.127
72
P CRD132 Cardiac Conduction Defect 43 0.122
73
c CRN176 Coronary Heart Disease 9 18 0.121
74
PLM033 Pulmonary Embolism 60 0.120
75
SNT004 Sinoatrial Node Dysfunction and Deafness 25 0.117
76
END021 Endomyocardial Fibrosis 49 0.117
77
THR024 Thrombosis 57 0.114
78
ADL002 Adult Syndrome 52 0.112
79
P DYS021 Dysautonomia 44 0.112
80
c MYC058 Myocardial Infarction 2 28 0.112
81
c HYP595 Hypertension, Essential 69 0.111
82
P END033 Endocarditis 54 0.110
83
HYP005 Hypokalemia 51 0.110
84
HRT008 Heart Conduction Disease 42 0.110
85
ART021 Arteriosclerosis 58 0.108
86
c ACT076 Acute Myocarditis 42 0.106
87
PRC013 Pericarditis 51 0.105
88
P MTR012 Mitral Valve Disease 58 0.104
89
CRN030 Coronary Stenosis 51 0.104
90
P MSC005 Muscular Dystrophy 65 0.103
91
P MSC007 Muscle Hypertrophy 58 0.102
92
STS002 Situs Inversus 46 0.101
93
P RSP003 Respiratory Failure 71 0.101
94
UNV002 Univentricular Heart 26 0.101
95
ART031 Aortic Coarctation 43 0.099
96
c CRN177 Coronary Heart Disease 7 20 0.097
97
P MYP004 Myopathy 67 0.097
98
HYD012 Hydrops Fetalis 43 0.097
99
END074 Endocardium Disease 26 0.097
100
P MYT002 Myotonic Dystrophy 48 0.097
101
GNT019 Giant Cell Myocarditis 31 0.097
102
INT007 Intermediate Coronary Syndrome 50 0.095
103
AND005 Androgen Insensitivity Syndrome, Mild 16 0.095
104
VND001 Vein Disease 47 0.095
105
NXS001 Naxos Disease 46 0.094
106
ACR041 Acromelic Frontonasal Dysostosis 45 0.092
107
ART017 Aortic Disease 57 0.092
108
EBS001 Ebstein Anomaly 45 0.091
109
BRT030 Birth Defects 43 0.091
110
ARR026 Arrhythmogenic Right Ventricular Dysplasia 1 41 0.091
111
HSB001 His Bundle Tachycardia 22 0.090
112
STR067 Stroke, Ischemic 75 0.090
113
ARR030 Arrhythmogenic Right Ventricular Dysplasia 2 41 0.089
114
FNT004 Fainting 33 0.089
115
CRB009 Cerebritis 39 0.087
116
FBR012 Fabry Disease 69 0.085
117
END072 Endotheliitis 42 0.085
118
CHT001 Chaotic Atrial Tachycardia 7 0.085
119
P PHC003 Pheochromocytoma 71 0.084
120
HPT074 Hepatic Adenoma, Somatic 50 0.083
121
HNM002 Hinman Syndrome 25 0.083
122
ANG054 Angina Pectoris 50 0.083
123
P OBS005 Obesity 92 0.082
124
CRT028 Cor Triatriatum 22 0.082
125
P AMY004 Amyloidosis 65 0.082
126
ALR002 Al-Raqad Syndrome 36 0.082
127
ARR025 Arrhythmogenic Right Ventricular Dysplasia 5 44 0.081
128
ARR029 Arrhythmogenic Right Ventricular Dysplasia 8 37 0.081
129
VSC007 Vascular Disease 67 0.080
130
CNS002 Constrictive Pericarditis 34 0.080
131
PCK002 Pick Disease 68 0.080
132
MSC004 Muscle Tissue Disease 34 0.080
133
SNT005 Sinoatrial Node Disease 36 0.079
134
c CRN173 Coronary Heart Disease 8 18 0.079
135
MRF001 Marfan Syndrome 73 0.079
136
KDS001 Kid Syndrome 53 0.079
137
END020 Endocardial Fibroelastosis 44 0.079
138
c MTR002 Mitral Valve Insufficiency 44 0.079
139
RSP006 Respiratory System Disease 58 0.078
140
CHG001 Chagas Disease 67 0.076
141
P NRP001 Neuropathy 59 0.076
142
ARR037 Arrhythmogenic Right Ventricular Dysplasia 12 25 0.076
143
INF034 Infective Endocarditis 51 0.076
144
ESN011 Eisenmenger Syndrome 45 0.076
145
HYP540 Hypertension, Diastolic 39 0.076
146
P THY032 Thyroiditis 54 0.075
147
BLD053 Blood Platelet Disease 46 0.075
148
CHL071 Child Syndrome 58 0.074
149
CRN017 Coronary Thrombosis 48 0.073
150
c SHR030 Short Qt Syndrome 44 0.073
151
CHR066 Chronic Fatigue Syndrome 64 0.072
152
P THR014 Thrombocytopenia 64 0.071
153
P RST002 Restrictive Cardiomyopathy 50 0.071
154
c SCK017 Sick Sinus Syndrome 1 29 0.071
155
PTN001 Patent Foramen Ovale 55 0.071
156
LNG099 Lung Disease 64 0.070
157
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.070
158
MYC005 Myocardial Stunning 44 0.070
159
ARR035 Arrhythmogenic Right Ventricular Dysplasia 9 40 0.070
160
ARR040 Arrhythmogenic Right Ventricular Dysplasia 10 27 0.070
161
SLP005 Sleep Disorder 53 0.070
162
P ALX003 Alexander Disease 63 0.068
163
DCH001 Duchenne Muscular Dystrophy 79 0.068
164
c CRD099 Cardiomyopathy, Dilated, 1e 52 0.068
165
P EPL164 Epilepsy 66 0.067
166
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.067
167
CRD001 Cardiac Tamponade 44 0.066
168
CHR413 Chronic Myocardial Ischemia 41 0.066
169
ATN004 Autonomic Neuropathy 45 0.065
170
MDS022 Mediastinitis 41 0.065
171
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.065
172
ARR041 Arrhythmogenic Right Ventricular Dysplasia, Familial, 13 20 0.065
173
ARR034 Arrhythmogenic Right Ventricular Dysplasia 6 17 0.065
174
CRB039 Cerebrovascular Disease 63 0.065
175
P MSC033 Muscle Disorders 52 0.064
176
ADJ001 Adjustment Disorder 38 0.063
177
P LYM118 Lymphoma 69 0.063
178
P BPL003 Bipolar Disorder 62 0.063
179
LPM004 Lipoma 60 0.063
180
P HYP076 Hyperthyroidism 55 0.063
181
NRN002 Neuronitis 41 0.063
182
P MNN013 Meningitis 67 0.062
183
WLL006 Wells Syndrome 59 0.062
184
BRN106 Burns 52 0.062
185
GDS001 Good Syndrome 44 0.062
186
P THY054 Thyrotoxic Periodic Paralysis 48 0.061
187
c SCK014 Sick Sinus Syndrome 2 27 0.061
188
HYP266 Hypoxia 56 0.060
189
P RNL015 Renal Hypertension 48 0.060
190
ARR036 Arrhythmogenic Right Ventricular Dysplasia 3 15 0.060
191
HTR003 Heterotaxy 44 0.059
192
P HRT035 Heart Block, Congenital 38 0.059
193
ARR033 Arrhythmogenic Right Ventricular Dysplasia 4 17 0.059
194
CST001 Costello Syndrome 68 0.059
195
TXC005 Toxic Shock Syndrome 60 0.058
196
P DRM010 Dermatomyositis 62 0.058
197
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.057
198
P EPN002 Ependymoma 53 0.057
199
HRT007 Heart Cancer 46 0.057
200
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.057
201
P HRT017 Heart Tumor 32 0.057
202
c ADL079 Adult Heart Tumor 16 0.057
203
INT084 Intrinsic Cardiomyopathy 34 0.057
204
ACR007 Acromegaly 66 0.056
205
PRP080 Peripheral Artery Disease 37 0.056
206
c PST001 Posterior Myocardial Infarction 31 0.056
207
ART016 Aortic Aneurysm 69 0.055
208
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 54 0.055
209
ANR010 Aneurysm of Sinus of Valsalva 26 0.055
210
PST055 Postural Hypotension 36 0.055
211
KWS002 Kawasaki Disease 70 0.054
212
PPL022 Papilloma 55 0.054
213
CSY001 C Syndrome 50 0.054
214
P BLD051 Blood Coagulation Disease 42 0.054
215
ARR005 Arrhythmogenic Right Ventricular Dysplasia/cardiomyopathy 2 12 0.054
216
ARR008 Arrhythmogenic Right Ventricular Dysplasia/cardiomyopathy 5 12 0.054
217
LPD004 Lipoid Nephrosis 48 0.053
218
CRD180 Cardiomyopathy, Dilated, with Woolly Hair and Keratoderma 36 0.053
219
P AST005 Asthma 82 0.052
220
P GLM045 Glioma 60 0.052
221
P AND016 Andersen Syndrome 58 0.052
222
c THR092 Thrombophilia Due to Thrombin Defect 54 0.052
223
CRD118 Cardiovascular Cancer 44 0.052
224
DBL010 Double-Orifice Mitral Valve 16 0.052
225
ARR006 Arrhythmogenic Right Ventricular Dysplasia/cardiomyopathy 3 10 0.052
226
c SCK022 Sick Sinus Syndrome 3 22 0.050
227
P SHR029 Short Syndrome 58 0.050
228
HTC002 Hutchinson-Gilford Progeria 57 0.050
229
c PND001 Pain Disorder 54 0.050
230
P CHR345 Chronic Pain 50 0.050
231
HYP017 Hypophosphatemia 43 0.050
232
BCK001 Becker Muscular Dystrophy 69 0.050
233
FCT008 Factitious Disorder 41 0.050
234
c AST037 Asthma 1 29 0.050
235
P PLM064 Pulmonary Sequestration 27 0.050
236
FML213 Familial Isolated Arrhythmogenic Ventricular Dysplasia, Right Dominant Form 25 0.050
237
ATR055 Atrial Septal Aneurysm 24 0.050
238
ATR024 Atrial Fibrillation and Stroke 22 0.050
239
ARR009 Arrhythmogenic Right Ventricular Dysplasia/cardiomyopathy 6 8 0.050
240
P NRV007 Nervous System Disease 71 0.048
241
ALN001 Aland Island Eye Disease 45 0.048
242
ARR004 Arrhythmogenic Right Ventricular Dysplasia/cardiomyopathy 1 10 0.048
243
ANX002 Anxiety Disorder 67 0.048
244
c SRC025 Sarcoidosis 1 61 0.048
245
MLG056 Malignant Hyperthermia 58 0.048
246
NWC001 Newcastle Disease 54 0.048
247
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 41 0.048
248
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 39 0.048
249
NTR005 Nutritional Deficiency Disease 36 0.048
250
EXF001 Exfoliation Syndrome 57 0.046
251
P PLN008 Peeling Skin Syndrome 45 0.046
252
P TBR001 Tuberous Sclerosis 67 0.046
253
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.046
254
P ATX004 Ataxia 53 0.046
255
CRB085 Cerebral Hemorrhage 46 0.046
256
PHY002 Physical Disorder 43 0.046
257
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.046
258
BRN080 Brain Ischemia 41 0.046
259
PLM137 Palmoplantar Keratoderma and Woolly Hair 34 0.046
260
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 33 0.046
261
FRS012 First-Degree Atrioventricular Block 30 0.046
262
CHR033 Chordoid Glioma 30 0.046
263
c CRD204 Cardiomyopathy, Hypertrophic, 10 28 0.046
264
FML214 Familial Isolated Arrhythmogenic Ventricular Dysplasia, Biventricular Form 24 0.046
265
FML215 Familial Isolated Arrhythmogenic Ventricular Dysplasia, Left Dominant Form 24 0.046
266
VNT031 Ventricular Extrasystoles with Syncope, Perodactyly, and Robin Sequence 11 0.046
267
P LMY004 Leiomyosarcoma 55 0.045
268
PRV004 Periventricular Leukomalacia 48 0.045
269
LPM005 Lipomatosis 47 0.045
270
LKM006 Leukomalacia 43 0.045
271
PRD011 Proud Syndrome 42 0.045
272
CNV002 Conversion Disorder 41 0.045
273
CRN019 Coronary Artery Vasospasm 40 0.045
274
ADP007 Adie Pupil 34 0.045
275
NTR041 N-Terminal Acetyltransferase Deficiency 33 0.045
276
P ATX010 Ataxia Neuropathy Spectrum 30 0.045
277
DFC004 Deficiency Anemia 64 0.043
278
PLM129 Pulmonary Disease, Chronic Obstructive 63 0.043
279
HYP066 Hyperglycemia 61 0.043
280
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.043
281
CTS003 Coats Disease 57 0.043
282
ADM013 Adamantinoma of Long Bones 57 0.043
283
PRT011 Protein C Deficiency 52 0.043
284
BRN071 Brain Injury 52 0.043
285
c RCS002 Recessive Dystrophic Epidermolysis Bullosa 50 0.043
286
LRN003 Learning Disability 49 0.043
287
NSD001 Nose Disease 48 0.043
288
P MYF003 Myofibrillar Myopathy 42 0.043
289
NSY001 N Syndrome 36 0.043
290
MTR027 Mitral Atresia 17 0.043
291
LYM017 Lyme Disease 63 0.042
292
STT001 Status Epilepticus 59 0.042
293
PRP019 Peripheral Nervous System Disease 55 0.042
294
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 27 0.042
295
P MYS003 Myasthenia Gravis 67 0.041
296
CMM005 Common Cold 59 0.041
297
GTR002 Goiter 52 0.041
298
IRN001 Iron Deficiency Anemia 52 0.041
299
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.041
300
BCK006 Back Pain 43 0.041
301
BRN105 Burn Scar 37 0.041
302
P ATR081 Atrial Standstill 37 0.041
303
MYX004 Myxedema 35 0.041
304
c PLN017 Peeling Skin Syndrome 1 34 0.041
305
CNT017 Central Nervous System Origin Vertigo 24 0.041
306
P BRS047 Breast Cancer 100 0.040
307
BRN028 Brain Cancer 70 0.040
308
DWN001 Down Syndrome 66 0.040
309
P FRD001 Friedreich Ataxia 62 0.040
310
NRM005 Neuromuscular Disease 56 0.040
311
P EMR001 Emery-Dreifuss Muscular Dystrophy 55 0.040
312
c LNG092 Long Qt Syndrome-3 49 0.040
313
LMB062 Limb Ischemia 48 0.040
314
FBR054 Fibroma 46 0.040
315
CRN041 Carnitine-Acylcarnitine Translocase Deficiency 43 0.040
316
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.040
317
BLD054 Blood Protein Disease 37 0.040
318
RDN001 Reading Disorder 34 0.040
319
PRT048 Partial Atrioventricular Canal 30 0.040
320
c CRD202 Cardiomyopathy, Hypertrophic, 12 28 0.040
321
SPN331 Spondyloocular Syndrome 27 0.040
322
CRD054 Cardiac Arrhythmia, Ankyrin-B-Related 23 0.040
323
BRR004 Baroreflex Failure 22 0.040
324
LVC002 Levocardia 18 0.040
325
HRT029 Heart Tumor of the Child 15 0.040
326
P LKM002 Leukemia 71 0.037
327
P GLB002 Glioblastoma 68 0.037
328
MTH009 Mouth Disease 61 0.037
329
P EXN002 Exanthem 57 0.037
330
P MYS005 Myositis 57 0.037
331
GST050 Gastrointestinal System Disease 56 0.037
332
PLN006 Poland Syndrome 54 0.037
333
TRM010 Traumatic Brain Injury 52 0.037
334
QDR001 Quadriplegia 52 0.037
335
CRC006 Carcinoid Syndrome 52 0.037
336
GNR004 Generalized Anxiety Disorder 51 0.037
337
RHM028 Rheumatic Heart Disease 50 0.037
338
MVM001 Movement Disease 49 0.037
339
HMN009 Hemangioblastoma 45 0.037
340
HDN002 Head Injury 45 0.037
341
RGH009 Right Atrial Isomerism 44 0.037
342
PHC013 Phaeochromocytoma 41 0.037
343
c PRG106 Progressive Muscular Dystrophy 40 0.037
344
AMR003 Amaurosis Fugax 38 0.037
345
SPC003 Specific Developmental Disorder 38 0.037
346
CYN002 Cyanosis, Transient Neonatal 28 0.037
347
c CRD197 Cardiomyopathy, Hypertrophic, 16 27 0.037
348
c CRD211 Cardiomyopathy, Hypertrophic, 17 26 0.037
349
MNT001 Mantle Cell Lymphoma 72 0.036
350
P NRM001 Neuromyelitis Optica 60 0.036
351
UND005 Undifferentiated Pleomorphic Sarcoma 44 0.036
352
c SHR033 Short Qt Syndrome 3 27 0.036
353
ATR048 Atrial Tachyarrhythmia with Short Pr Interval 27 0.036
354
ATM052 Autoimmune Disease 1 25 0.036
355
ATM013 Autoimmune Disease of Cardiovascular System 13 0.036
356
DGT004 Digitalis Poisoning 11 0.036
357
P LNG032 Lung Cancer 95 0.034
358
P OVR042 Ovarian Cancer 76 0.034
359
P ADN016 Adenocarcinoma 69 0.034
360
INC002 Inclusion Body Myositis 66 0.034
361
P CNJ013 Conjunctivitis 64 0.034
362
P RCK004 Rickets 61 0.034
363
KRN002 Kearns-Sayre Syndrome 61 0.034
364
P NRV006 Nervous System Cancer 60 0.034
365
P OCL013 Oculodentodigital Dysplasia 59 0.034
366
P PRP029 Porphyria 59 0.034
367
P CTR002 Cataract 58 0.034
368
RHB003 Rhabdomyosarcoma 57 0.034
369
P THY023 Thymoma 57 0.034
370
P HYP613 Hypophosphatemic Rickets 57 0.034
371
P CHN012 Chondrosarcoma 56 0.034
372
P LPD010 Lipodystrophy 55 0.034
373
HDC001 Headache 54 0.034
374
LMY002 Leiomyoma 54 0.034
375
RHM001 Rheumatic Fever 54 0.034
376
P BRC006 Brachydactyly 54 0.034
377
CND002 Conduct Disorder 54 0.034
378
P JRV003 Jervell and Lange-Nielsen Syndrome 53 0.034
379
P PLY041 Polymyositis 52 0.034
380
P PRM002 Primary Hyperoxaluria 51 0.034
381
FML038 Female Reproductive Organ Cancer 50 0.034
382
BRN022 Bronchiectasis 50 0.034
383
PRP016 Paraplegia 49 0.034
384
OST011 Osteomalacia 49 0.034
385
INF058 Inflammatory Myofibroblastic Tumor 47 0.034
386
PTT009 Pituitary Gland Disease 47 0.034
387
INC022 Inclusion-Cell Disease 46 0.034
388
P PLG001 Pelger-Huet Anomaly 45 0.034
389
HYP085 Hypothalamic Disease 44 0.034
390
PLS016 Plasma Cell Leukemia 42 0.034
391
SXL003 Sexual Disorder 42 0.034
392
FML036 Familial Periodic Paralysis 39 0.034
393
PHS001 Phosphorus Metabolism Disease 38 0.034
394
P BRN030 Brain Ependymoma 32 0.034
395
SPR035 Superior Vena Cava Syndrome 31 0.034
396
CHR055 Chordoid Meningioma 29 0.034
397
SBC014 Subclavian Steal Syndrome 28 0.034
398
c ATR061 Atrial Fibrillation, Familial, 10 26 0.034
399
SCN049 Second-Degree Atrioventricular Block 24 0.034
400
c LNR014 Linear Skin Defects with Multiple Congenital Anomalies 3 18 0.034
401
c BNG076 Benign Exophthalmos Syndrome 15 0.034
402
PRP050 Peripheral Arterial Occlusive Disease 1 14 0.034
403
SGM003 Segmentation Syndrome 1 12 0.034
404
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 78 0.029
405
ESP021 Esophageal Cancer 76 0.029
406
P LFR001 Li-Fraumeni Syndrome 75 0.029
407
MLT021 Multiple System Atrophy 70 0.029
408
SQM006 Squamous Cell Carcinoma 70 0.029
409
P BCL006 B-Cell Lymphomas 65 0.029
410
P AST007 Astrocytoma 65 0.029
411
P ART023 Arthropathy 64 0.029
412
PNC041 Pancreatic Ductal Adenocarcinoma 64 0.029
413
P LNG064 Lung Cancer Susceptibility 3 62 0.029
414
P ESP024 Esophagitis 61 0.029
415
CRB011 Cerebrotendinous Xanthomatosis 61 0.029
416
DRR010 Darier Disease 60 0.029
417
FLL027 Fallopian Tube Carcinoma 60 0.029
418
CRV038 Cervical Squamous Cell Carcinoma 60 0.029
419
ETN001 Eating Disorder 58 0.029
420
c FML108 Familial Breast Cancer 57 0.029
421
ADR005 Adrenal Carcinoma 57 0.029
422
ORL011 Oral Cancer 56 0.029
423
P SML001 Small Cell Carcinoma 56 0.029
424
c MYT020 Myotonic Dystrophy 2 56 0.029
425
JNT002 Joint Disorders 55 0.029
426
P FNC043 Fanconi Anemia, Complementation Group E 55 0.029
427
P EPD009 Epidermolysis Bullosa Dystrophica 55 0.029
428
P PRG013 Paraganglioma 54 0.029
429
c PRM126 Primary Peritoneal Carcinoma 54 0.029
430
P INT030 Intracranial Aneurysm 54 0.029
431
HLY001 Hailey-Hailey Disease 53 0.029
432
TRN018 Transitional Cell Carcinoma 53 0.029
433
c INS002 in Situ Carcinoma 53 0.029
434
BLT006 Bilateral Breast Cancer 53 0.029
435
HYP609 Hypophosphatemic Rickets, X-Linked Dominant 52 0.029
436
P TRT010 Teratoma 52 0.029
437
c BRS049 Breast Carcinoma in Situ 51 0.029
438
CRT049 Critical Limb Ischemia 51 0.029
439
DBT062 Diabetic Foot Ulcers 51 0.029
440
DCT002 Ductal Carcinoma in Situ 51 0.029
441
P PMP005 Pemphigus Vulgaris 51 0.029
442
KLD001 Keloids 51 0.029
443
MYL001 Myelitis 51 0.029
444
PMP001 Pemphigus 50 0.029
445
RNL007 Renal Tubular Acidosis 50 0.029
446
BRN082 Bernard-Soulier Syndrome, Type C 50 0.029
447
MND007 Mandibuloacral Dysplasia 49 0.029
448
P TRN034 Transverse Myelitis 49 0.029
449
RYN003 Reynolds Syndrome 49 0.029
450
c MCL062 Mucolipidosis Ii Alpha/beta 48 0.029
451
c SPR009 Sporadic Breast Cancer 47 0.029
452
P GLM040 Glioma Susceptibility 1 47 0.029
453
c CLL013 Cell Type Cancer 46 0.029
454
XNT003 Xanthomatosis 46 0.029
455
P ACT150 Acute Adrenal Insufficiency 45 0.029
456
P RPR003 Reproductive Organ Cancer 44 0.029
457
PRG004 Progeria 44 0.029
458
SHH001 Sheehan Syndrome 44 0.029
459
c CNG012 Congenital Generalized Lipodystrophy 44 0.029
460
c LNG096 Long Qt Syndrome 15 44 0.029
461
PPL007 Papillary Serous Adenocarcinoma 43 0.029
462
PLM029 Palmoplantar Keratosis 43 0.029
463
c FML191 Familial Long Qt Syndrome 42 0.029
464
P ECT007 Ectodermal Dysplasia/skin Fragility Syndrome 42 0.029
465
P RST011 Restrictive Dermopathy, Lethal 41 0.029
466
SPR007 Superior Mesenteric Artery Syndrome 41 0.029
467
CRB002 Cerebral Primitive Neuroectodermal Tumor 41 0.029
468
IRN002 Iron Metabolism Disease 41 0.029
469
PNM013 Pneumococcal Meningitis 41 0.029
470
ONC003 Oncogenic Osteomalacia 41 0.029
471
P CNG390 Congenital Pulmonary Airway Malformation 41 0.029
472
c PRM023 Pre-Malignant Neoplasm 41 0.029
473
MLT008 Multinodular Goiter 41 0.029
474
RNS001 Raine Syndrome 40 0.029
475
OVR060 Ovary Epithelial Cancer 40 0.029
476
c SBC007 Subacute Thyroiditis 40 0.029
477
MYC012 Mycetoma 40 0.029
478
c FBR084 Fibromatosis, Gingival, 1 39 0.029
479
HYP135 Hypophosphatemic Rickets with Hypercalciuria 39 0.029
480
P HMF004 Hemifacial Spasm 39 0.029
481
BRS090 Breast Reconstruction 38 0.029
482
c LKD007 Leukodystrophy, Adult-Onset, Autosomal Dominant 38 0.029
483
ICH020 Ichthyosis Prematurity Syndrome 38 0.029
484
SYN003 Synchronous Bilateral Breast Carcinoma 38 0.029
485
EXT035 Extrinsic Cardiomyopathy 37 0.029
486
MLG076 Malignant Ovarian Surface Epithelial-Stromal Neoplasm 37 0.029
487
MLG098 Malignant Mixed Mullerian Tumor 36 0.029
488
c EPD044 Epidermolysis Bullosa Dystrophica, Ar 36 0.029
489
EPD022 Epidermolysis Bullosa Pruriginosa 36 0.029
490
GRV012 Grover's Disease 36 0.029
491
c ATS239 Autosomal Recessive Hypophosphatemic Rickets 35 0.029
492
ENT004 Enthesopathy 35 0.029
493
LNT008 Lentiginosis, Inherited Patterned 34 0.029
494
EPD033 Epidermolysis Bullosa, Lethal Acantholytic 34 0.029
495
UTR011 Uterine Corpus Serous Adenocarcinoma 34 0.029
496
P WLL010 Woolly Hair Syndrome 34 0.029
497
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 31 0.029
498
CHR463 Chronic Actinic Dermatitis 31 0.029
499
CYS015 Cystadenofibroma 30 0.029
500
HNS001 Hansen's Disease 30 0.029
501
OVR048 Ovarian Cystadenoma 29 0.029
502
GRN016 Grant Syndrome 29 0.029
503
c PLN021 Peeling Skin Syndrome 3 29 0.029
504
GLY012 Glycogen-Rich Clear Cell Breast Carcinoma 29 0.029
505
TRG001 Trigonitis 28 0.029
506
c ATR038 Atrial Fibrillation, Familial, 3 27 0.029
507
THY001 Thyroid Crisis 27 0.029
508
MDD005 Middle Lobe Syndrome 27 0.029
509
NRG005 Neurogenic Hypertension 27 0.029
510
P ATS208 Autosomal Dominant Macrothrombocytopenia 27 0.029
511
CCN009 Cocaine Intoxication 20 0.029
512
ARL004 Aural Atresia, Congenital 20 0.029
513
c BRG010 Brugada Syndrome 8 20 0.029
514
MYH015 Myh-9 Related Disease 19 0.029
515
CRT060 Cor Triatriatum Sinister 18 0.029
516
EMR002 Emerinopathy 18 0.029
517
WSC001 Wisconsin Syndrome 14 0.029
518
ADS006 Aids - Neurological Complications 12 0.029