Search results for "arrhythmia"

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

2481 hits were found for 'arrhythmia'

# Family MCID Name MIFTS Score
1
CRD054 Cardiac Arrhythmia, Ankyrin-B-Related 23 3.396
2
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 30 3.391
3
LNG104 Language Delay and Attention Deficit-Hyperactivity Disorder/cognitive Impairment with or Without Cardiac Arrhythmia 7 3.385
4
PHC009 Phocomelia Ectrodactyly Deafness Sinus Arrhythmia 10 2.795
5
PHC016 Phocomelia-Ectrodactyly, Ear Malformation, Deafness, and Sinus Arrhythmia 15 2.782
6
ANK016 Ankyrin-B Syndrome 6 2.771
7
c CRD099 Cardiomyopathy, Dilated, 1e 52 2.764
8
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 2.247
9
WLF001 Wolff-Parkinson-White Syndrome 56 2.010
10
SNT004 Sinoatrial Node Dysfunction and Deafness 25 2.010
11
SDD004 Sudden Arrhythmia Death Syndrome 15 2.010
12
RCR029 Recurrent Metabolic Encephalomyopathic Crises-Rhabdomyolysis-Cardiac Arrhythmia-Intellectual Disability Syndrome 2 1.963
13
NTR041 N-Terminal Acetyltransferase Deficiency 33 1.955
14
c ATS333 Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2x 15 1.955
15
P CRD011 Cardiomyopathy 68 0.118
16
P ATR011 Atrial Fibrillation 66 0.111
17
P HRT032 Heart Disease 75 0.107
18
P MYC007 Myocardial Infarction 79 0.103
19
c FML001 Familial Atrial Fibrillation 58 0.095
20
SDD007 Sudden Cardiac Death 47 0.093
21
P LNG028 Long Qt Syndrome 64 0.088
22
c VNT013 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1 49 0.087
23
c CRN175 Coronary Heart Disease 4 19 0.084
24
P CRD132 Cardiac Conduction Defect 43 0.082
25
c CRN172 Coronary Heart Disease 3 19 0.082
26
VNT011 Ventricular Fibrillation, Familial, 1 41 0.079
27
CRD119 Cardiac Arrest 61 0.075
28
SYN036 Syncope 47 0.074
29
c DLT002 Dilated Cardiomyopathy 76 0.073
30
P BRG001 Brugada Syndrome 59 0.073
31
CNG034 Congestive Heart Failure 72 0.070
32
c ACT075 Acute Myocardial Infarction 60 0.070
33
ATR060 Atrial Standstill, Digenic 51 0.070
34
SNG003 Single Ventricular Heart 22 0.070
35
P CRN178 Coronary Heart Disease 6 21 0.069
36
ISC004 Ischemia 61 0.066
37
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 60 0.065
38
P CRN211 Coronary Artery Disease 74 0.060
39
c CRN174 Coronary Heart Disease 2 20 0.060
40
P SCK002 Sick Sinus Syndrome 50 0.059
41
P PRX010 Paroxysmal Ventricular Fibrillation 37 0.059
42
CRD003 Cardiac Sarcoidosis 42 0.056
43
ISC006 Ischemic Heart Disease 68 0.054
44
c CRN214 Coronary Heart Disease 5 22 0.054
45
HYP005 Hypokalemia 51 0.050
46
P MYT002 Myotonic Dystrophy 48 0.050
47
FNT004 Fainting 33 0.050
48
P MSC005 Muscular Dystrophy 65 0.049
49
ATR024 Atrial Fibrillation and Stroke 22 0.049
50
P MYC008 Myocarditis 54 0.047
51
PRP027 Peripheral Vascular Disease 69 0.045
52
PRN021 Paranasal Sinus Disease 49 0.045
53
NSL022 Nasal Cavity Disease 38 0.045
54
TTR001 Tetralogy of Fallot 71 0.043
55
ART111 Artery Disease 55 0.043
56
c MYC058 Myocardial Infarction 2 28 0.043
57
ANR040 Aneurysm 57 0.040
58
SYS003 Systolic Heart Failure 43 0.040
59
P MYP004 Myopathy 67 0.038
60
P EPL164 Epilepsy 66 0.038
61
P SLP006 Sleep Apnea 61 0.038
62
P NRP001 Neuropathy 59 0.038
63
ART021 Arteriosclerosis 58 0.038
64
P AND016 Andersen Syndrome 58 0.038
65
CRN030 Coronary Stenosis 51 0.038
66
HYP006 Hypertensive Heart Disease 50 0.038
67
ATR057 Atrioventricular Block 49 0.038
68
TRN044 Transposition of the Great Arteries 48 0.038
69
ATN004 Autonomic Neuropathy 45 0.038
70
HRT012 Heart Valve Disease 40 0.038
71
P CRD194 Cardiomyopathy, Familial Hypertrophic 62 0.036
72
HYP056 Hypoglycemia 61 0.036
73
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 56 0.036
74
SLP005 Sleep Disorder 53 0.036
75
VND001 Vein Disease 47 0.036
76
SKN023 Skin Tag 44 0.036
77
STR067 Stroke, Ischemic 75 0.033
78
CHG001 Chagas Disease 67 0.033
79
P KDN018 Kidney Disease 66 0.033
80
OBS061 Obstructive Sleep Apnea 66 0.033
81
c LNG044 Long Qt Syndrome 1 62 0.033
82
RSP006 Respiratory System Disease 58 0.033
83
P SPS003 Spastic Diplegia 52 0.033
84
P LFT003 Left Ventricular Noncompaction 50 0.033
85
ATN002 Autonomic Nervous System Disease 48 0.033
86
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.033
87
c SHR030 Short Qt Syndrome 44 0.033
88
DBT002 Diabetic Autonomic Neuropathy 42 0.033
89
ATR055 Atrial Septal Aneurysm 24 0.033
90
c CRN173 Coronary Heart Disease 8 18 0.033
91
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.030
92
DCH001 Duchenne Muscular Dystrophy 79 0.030
93
c HYP595 Hypertension, Essential 69 0.030
94
VSC007 Vascular Disease 67 0.030
95
c CHR089 Chronic Kidney Failure 66 0.030
96
P ENC018 Encephalopathy 59 0.030
97
c LNG047 Long Qt Syndrome 2 57 0.030
98
NRM005 Neuromuscular Disease 56 0.030
99
P TMT001 Timothy Syndrome 55 0.030
100
P HYP076 Hyperthyroidism 55 0.030
101
END030 End Stage Renal Failure 55 0.030
102
BRN106 Burns 52 0.030
103
P MSC033 Muscle Disorders 52 0.030
104
INT007 Intermediate Coronary Syndrome 50 0.030
105
P MSC003 Muscular Atrophy 50 0.030
106
CSY001 C Syndrome 50 0.030
107
c LNG051 Long Qt Syndrome 6 49 0.030
108
c LNG092 Long Qt Syndrome-3 49 0.030
109
CRD137 Cardiogenic Shock 46 0.030
110
FDB001 Foodborne Botulism 45 0.030
111
RGH001 Right Bundle Branch Block 44 0.030
112
c LNG053 Long Qt Syndrome 9 44 0.030
113
c BRG005 Brugada Syndrome 1 40 0.030
114
CRB009 Cerebritis 39 0.030
115
MSC004 Muscle Tissue Disease 34 0.030
116
P HRT017 Heart Tumor 32 0.030
117
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 27 0.030
118
c BRG003 Brugada Syndrome 3 25 0.030
119
c CRN177 Coronary Heart Disease 7 20 0.030
120
c CRN176 Coronary Heart Disease 9 18 0.030
121
P RTT002 Rett Syndrome 77 0.027
122
BCK001 Becker Muscular Dystrophy 69 0.027
123
ATH003 Atherosclerosis 65 0.027
124
CRB039 Cerebrovascular Disease 63 0.027
125
c MYT021 Myotonic Dystrophy 1 63 0.027
126
P RFS001 Refsum Disease 63 0.027
127
P BPL003 Bipolar Disorder 62 0.027
128
P SDD001 Sudden Infant Death Syndrome 61 0.027
129
c CNT035 Central Nervous System Disease 60 0.027
130
P OCL013 Oculodentodigital Dysplasia 59 0.027
131
P MSC007 Muscle Hypertrophy 58 0.027
132
ART017 Aortic Disease 57 0.027
133
ADM013 Adamantinoma of Long Bones 57 0.027
134
P SZR006 Seizure Disorder 56 0.027
135
c CRD093 Cardiomyopathy, Dilated, 1a 55 0.027
136
CND002 Conduct Disorder 54 0.027
137
c ART101 Aortic Valve Disease 2 53 0.027
138
P JRV003 Jervell and Lange-Nielsen Syndrome 53 0.027
139
BRT005 Barth Syndrome 52 0.027
140
c LNG050 Long Qt Syndrome 5 51 0.027
141
PRC012 Pericardial Effusion 51 0.027
142
URN009 Urinary System Disease 50 0.027
143
P URF003 Urofacial Syndrome 1 50 0.027
144
ATN005 Autonomic Dysfunction 49 0.027
145
P THY054 Thyrotoxic Periodic Paralysis 48 0.027
146
HRT007 Heart Cancer 46 0.027
147
ADR038 Adermatoglyphia 46 0.027
148
ACR041 Acromelic Frontonasal Dysostosis 45 0.027
149
c LNG056 Long Qt Syndrome 12 45 0.027
150
CRD118 Cardiovascular Cancer 44 0.027
151
CRN041 Carnitine-Acylcarnitine Translocase Deficiency 43 0.027
152
BRT030 Birth Defects 43 0.027
153
HYP017 Hypophosphatemia 43 0.027
154
GLC008 Glucose Metabolism Disease 42 0.027
155
HRT008 Heart Conduction Disease 42 0.027
156
PRP009 Peripartum Cardiomyopathy 42 0.027
157
PRM025 Primary Bacterial Infectious Disease 41 0.027
158
ARR030 Arrhythmogenic Right Ventricular Dysplasia 2 41 0.027
159
c PRG106 Progressive Muscular Dystrophy 40 0.027
160
TSH001 Tsh Producing Pituitary Tumor 37 0.027
161
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.027
162
INF013 Inferior Myocardial Infarction 35 0.027
163
IMP003 Impaired Renal Function Disease 34 0.027
164
c BRG006 Brugada Syndrome 2 33 0.027
165
GNT019 Giant Cell Myocarditis 31 0.027
166
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 28 0.027
167
CPT005 Cpt Ii Deficiency, Lethal Neonatal 25 0.027
168
CNT017 Central Nervous System Origin Vertigo 24 0.027
169
c BRG004 Brugada Syndrome 4 22 0.027
170
HSB001 His Bundle Tachycardia 22 0.027
171
c ADL079 Adult Heart Tumor 16 0.027
172
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.023
173
P PLM037 Pulmonary Hypertension 79 0.023
174
P NRV007 Nervous System Disease 71 0.023
175
P RSP003 Respiratory Failure 71 0.023
176
KWS002 Kawasaki Disease 70 0.023
177
FBR012 Fabry Disease 69 0.023
178
CST001 Costello Syndrome 68 0.023
179
ANX002 Anxiety Disorder 67 0.023
180
SKN016 Skin Disease 66 0.023
181
ACR007 Acromegaly 66 0.023
182
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.023
183
P KDN017 Kidney Cancer 65 0.023
184
LNG099 Lung Disease 64 0.023
185
c TBR024 Tuberous Sclerosis-1 63 0.023
186
SPN186 Spinal Cord Injury 63 0.023
187
P SYS005 Systemic Scleroderma 61 0.023
188
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.023
189
WLL006 Wells Syndrome 59 0.023
190
CHL071 Child Syndrome 58 0.023
191
P EXN002 Exanthem 57 0.023
192
P HYP192 Hypocalcemia, Autosomal Dominant 56 0.023
193
HYP266 Hypoxia 56 0.023
194
P PLY019 Polyneuropathy 56 0.023
195
FCL014 Focal Epilepsy 55 0.023
196
c PND001 Pain Disorder 54 0.023
197
KDS001 Kid Syndrome 53 0.023
198
MNT002 Mental Depression 53 0.023
199
ADL002 Adult Syndrome 52 0.023
200
P PLY041 Polymyositis 52 0.023
201
c EHL055 Ehlers-Danlos Syndrome, Type Iii 50 0.023
202
LRN003 Learning Disability 49 0.023
203
NSD001 Nose Disease 48 0.023
204
THL018 Thalassemia Major 48 0.023
205
CCN002 Cocaine Abuse 48 0.023
206
P RNL015 Renal Hypertension 48 0.023
207
DBT084 Diabetes Mellitus, Ketosis-Prone 47 0.023
208
PRP021 Peripheral Nervous System Neoplasm 46 0.023
209
c MCR113 Microvascular Complications of Diabetes 3 45 0.023
210
CRB004 Cerebral Artery Occlusion 45 0.023
211
GDS001 Good Syndrome 44 0.023
212
MYC005 Myocardial Stunning 44 0.023
213
c LNG057 Long Qt Syndrome 13 44 0.023
214
c CNT015 Central Sleep Apnea 44 0.023
215
c DBT040 Diabetes Mellitus, Insulin-Dependent, 2 43 0.023
216
P PLM040 Pulmonary Valve Disease 43 0.023
217
c ACT076 Acute Myocarditis 42 0.023
218
AYM001 Ayme-Gripp Syndrome 41 0.023
219
ARR026 Arrhythmogenic Right Ventricular Dysplasia 1 41 0.023
220
CNV002 Conversion Disorder 41 0.023
221
c BRG007 Brugada Syndrome 5 39 0.023
222
ADJ001 Adjustment Disorder 38 0.023
223
GST007 Gastric Dilatation 38 0.023
224
SPC003 Specific Developmental Disorder 38 0.023
225
MDY003 Mody, Type Ii 36 0.023
226
c CRD199 Cardiomyopathy, Hypertrophic 6 36 0.023
227
c DBT082 Diabetes Mellitus, Insulin-Dependent, 12 36 0.023
228
SNT005 Sinoatrial Node Disease 36 0.023
229
CPL011 Capillary Malformations, Congenital, 1, Somatic, Mosaic 35 0.023
230
RDN001 Reading Disorder 34 0.023
231
c BRN108 Branchiootic Syndrome 1 34 0.023
232
INT084 Intrinsic Cardiomyopathy 34 0.023
233
c CRD187 Cardiomyopathy, Dilated, 3b 33 0.023
234
MYT003 Myotonic Disease 32 0.023
235
SBV001 Subvalvular Aortic Stenosis 31 0.023
236
ARR040 Arrhythmogenic Right Ventricular Dysplasia 10 27 0.023
237
c DBT056 Diabetes Mellitus, Insulin-Dependent, 4 25 0.023
238
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.023
239
c BRG009 Brugada Syndrome 7 24 0.023
240
c BRG008 Brugada Syndrome 6 24 0.023
241
MND006 Mondor Disease 21 0.023
242
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 21 0.023
243
c ATR074 Atrial Standstill 2 20 0.023
244
c LNG093 Long Qt Syndrome-11 20 0.023
245
MYT026 Myotonia Atrophica 18 0.023
246
VNT009 Ventricular Tachycardia, Idiopathic 16 0.023
247
ATR076 Atrophic Muscular Disease 15 0.023
248
P MLT019 Multiple Myeloma 83 0.019
249
P RNL014 Renal Cell Carcinoma 82 0.019
250
c AMY091 Amyotrophic Lateral Sclerosis 1 78 0.019
251
MRF001 Marfan Syndrome 73 0.019
252
P WSK001 Wiskott-Aldrich Syndrome 73 0.019
253
P HMC003 Hemochromatosis 72 0.019
254
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.019
255
P INF038 Influenza 72 0.019
256
P DMN001 Diamond-Blackfan Anemia 69 0.019
257
VNH007 Von Hippel-Lindau Syndrome 69 0.019
258
ATT013 Attention Deficit-Hyperactivity Disorder 69 0.019
259
P DRV001 Dravet Syndrome 69 0.019
260
PCK002 Pick Disease 68 0.019
261
WRN001 Werner Syndrome 67 0.019
262
LVR012 Liver Cirrhosis 67 0.019
263
P MNN013 Meningitis 67 0.019
264
P NNN008 Noonan Syndrome 1 67 0.019
265
CNT098 Central Core Disease 65 0.019
266
PTR006 Peters Anomaly 65 0.019
267
P AMY004 Amyloidosis 65 0.019
268
P SPN046 Spinal Muscular Atrophy 65 0.019
269
c MLT024 Multiple Endocrine Neoplasia Iia 64 0.019
270
P THL005 Thalassemia 64 0.019
271
P HYP086 Hypothyroidism 64 0.019
272
P HLP001 Holoprosencephaly 63 0.019
273
P FML161 Familial Mediterranean Fever, Ar 63 0.019
274
WGN006 Wegener Granulomatosis 63 0.019
275
LPT001 Leptospirosis 62 0.019
276
CNN005 Connective Tissue Disease 62 0.019
277
c SPN225 Spondyloarthropathy 1 62 0.019
278
c SRC025 Sarcoidosis 1 61 0.019
279
HYP066 Hyperglycemia 61 0.019
280
P DNT015 Dent Disease 61 0.019
281
P RCK004 Rickets 61 0.019
282
c LCL006 Localized Scleroderma 61 0.019
283
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 60 0.019
284
P NRV006 Nervous System Cancer 60 0.019
285
P DRR001 Diarrhea 60 0.019
286
RBR001 Roberts Syndrome 60 0.019
287
P GRV001 Graves' Disease 59 0.019
288
c GLY008 Glycogen Storage Disease Ii 59 0.019
289
LGN002 Legionellosis 59 0.019
290
CHL068 Cholestasis 59 0.019
291
P GT001 Gout 58 0.019
292
YLL002 Yellow Fever 58 0.019
293
P MTR012 Mitral Valve Disease 58 0.019
294
PRP084 Propionicacidemia 58 0.019
295
HMR004 Hemorrhagic Fever with Renal Syndrome 58 0.019
296
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 57 0.019
297
ADR005 Adrenal Carcinoma 57 0.019
298
THR024 Thrombosis 57 0.019
299
SNS001 Sensorineural Hearing Loss 57 0.019
300
TNS005 Tonsillitis 57 0.019
301
TRN015 Transient Cerebral Ischemia 56 0.019
302
c MYT020 Myotonic Dystrophy 2 56 0.019
303
PRP019 Peripheral Nervous System Disease 55 0.019
304
PTN001 Patent Foramen Ovale 55 0.019
305
c MSC124 Muscular Dystrophy, Congenital 55 0.019
306
P CHL002 Childhood Absence Epilepsy 55 0.019
307
P CDS001 Cadasil 55 0.019
308
P STC001 Stickler Syndrome 55 0.019
309
P EMR001 Emery-Dreifuss Muscular Dystrophy 55 0.019
310
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.019
311
GST037 Gastroparesis 54 0.019
312
PRP083 Porphyria, Acute Intermittent 54 0.019
313
P MCR129 Microvascular Complications of Diabetes 1 54 0.019
314
RHM001 Rheumatic Fever 54 0.019
315
NWC001 Newcastle Disease 54 0.019
316
P END033 Endocarditis 54 0.019
317
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.019
318
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 53 0.019
319
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 53 0.019
320
P LDD002 Liddle Syndrome 53 0.019
321
OLV001 Olivopontocerebellar Atrophy 53 0.019
322
LBR030 Leber Optic Atrophy 53 0.019
323
END040 Endogenous Depression 53 0.019
324
GTR002 Goiter 52 0.019
325
KRT002 Keratomalacia 52 0.019
326
ALL026 Allergic Hypersensitivity Disease 52 0.019
327
c PRX045 Peroxisome Biogenesis Disorder 1b 52 0.019
328
BRN071 Brain Injury 52 0.019
329
IMP005 Impotence 51 0.019
330
P PNM006 Pneumoconiosis 51 0.019
331
TRY001 Trypanosomiasis 51 0.019
332
INF034 Infective Endocarditis 51 0.019
333
c ART115 Aortic Valve Disease 1 50 0.019
334
DRG003 Drug Dependence 50 0.019
335
HYP037 Hyperhomocysteinemia 50 0.019
336
MCR088 Microscopic Polyangiitis 49 0.019
337
c ACT071 Acute Kidney Failure 49 0.019
338
P INT063 Intellectual Disability 49 0.019
339
SPR099 Supravalvar Aortic Stenosis 49 0.019
340
ERL001 Early Myoclonic Encephalopathy 49 0.019
341
c CNG464 Congenital Myopathy 49 0.019
342
MTN003 Motion Sickness 48 0.019
343
ADR012 Adrenal Gland Disease 48 0.019
344
DNN001 Danon Disease 48 0.019
345
CRN017 Coronary Thrombosis 48 0.019
346
THY030 Thyroid Gland Disease 48 0.019
347
PRT030 Parathyroid Gland Disease 47 0.019
348
PLM041 Pulmonary Valve Stenosis 47 0.019
349
VSC047 Vascular Malformation 45 0.019
350
ALN001 Aland Island Eye Disease 45 0.019
351
c HRT021 Heart Block, Progressive, Type Ia 44 0.019
352
HTR003 Heterotaxy 44 0.019
353
ARR025 Arrhythmogenic Right Ventricular Dysplasia 5 44 0.019
354
CRD001 Cardiac Tamponade 44 0.019
355
c LNG098 Long Qt Syndrome 14 44 0.019
356
P DYS021 Dysautonomia 44 0.019
357
AGR002 Agoraphobia 44 0.019
358
PHY002 Physical Disorder 43 0.019
359
DXT001 Dextrocardia 43 0.019
360
RNL097 Renal Artery Disease 43 0.019
361
SNS023 Sensory System Cancer 43 0.019
362
CRB008 Cerebral Atherosclerosis 43 0.019
363
c PRG126 Progressive Familial Heart Block 43 0.019
364
P CRB088 Cerebral Atrophy 43 0.019
365
c ART120 Arthrogryposis, Distal, Type 3 42 0.019
366
STT002 Status Asthmaticus 42 0.019
367
c FML191 Familial Long Qt Syndrome 42 0.019
368
SXL003 Sexual Disorder 42 0.019
369
MGL023 Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome, Somatic 42 0.019
370
P MYF003 Myofibrillar Myopathy 42 0.019
371
ANT018 Anthracosis 42 0.019
372
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.019
373
PRD011 Proud Syndrome 42 0.019
374
FCT008 Factitious Disorder 41 0.019
375
BRN080 Brain Ischemia 41 0.019
376
CRT008 Carotid Artery Dissection 41 0.019
377
PHC013 Phaeochromocytoma 41 0.019
378
SPC010 Speech and Communication Disorders 41 0.019
379
c CRD104 Cardiomyopathy, Dilated, 1p 41 0.019
380
THL017 Thalassemia Intermedia 40 0.019
381
SKN005 Skin Atrophy 40 0.019
382
CPT003 Cpt Deficiency, Hepatic, Type Ia 40 0.019
383
PLM068 Pulmonary Vein Stenosis 40 0.019
384
c CHR096 Chronic Pulmonary Heart Disease 40 0.019
385
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.019
386
ATN003 Autonomic Nervous System Neoplasm 40 0.019
387
ARR035 Arrhythmogenic Right Ventricular Dysplasia 9 40 0.019
388
CPT004 Cpt Deficiency, Hepatic, Type Ii 39 0.019
389
c MYP072 Myopathy, Myofibrillar, 1 39 0.019
390
PRN037 Prinzmetal's Variant Angina 39 0.019
391
c CRD190 Cardiomyopathy, Hypertrophic, 2 39 0.019
392
GND003 Gonadal Disease 39 0.019
393
HYP540 Hypertension, Diastolic 39 0.019
394
ADR009 Adrenal Cortex Disease 39 0.019
395
P HYP265 Hypotonia 38 0.019
396
ALC010 Alcoholic Cardiomyopathy 38 0.019
397
P FML187 Familial Hypertension 38 0.019
398
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.019
399
LYM029 Lymphedema-Distichiasis Syndrome 38 0.019
400
P HRT035 Heart Block, Congenital 38 0.019
401
ARR029 Arrhythmogenic Right Ventricular Dysplasia 8 37 0.019
402
BLD054 Blood Protein Disease 37 0.019
403
WTH001 Withdrawal Disorder 37 0.019
404
PRP080 Peripheral Artery Disease 37 0.019
405
c CNG031 Congenital Nervous System Abnormality 37 0.019
406
P ATR081 Atrial Standstill 37 0.019
407
c ALP005 Alpha Chain Disease 37 0.019
408
NSY001 N Syndrome 36 0.019
409
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 36 0.019
410
NTR005 Nutritional Deficiency Disease 36 0.019
411
c DLT016 Dilated Cardiomyopathy 1b 36 0.019
412
HTR014 Heterotaxy, Visceral, 1, X-Linked 36 0.019
413
ALR002 Al-Raqad Syndrome 36 0.019
414
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 35 0.019
415
c MLG132 Malignant Hyperthermia Susceptibility 1 35 0.019
416
c DBT058 Diabetes Mellitus, Insulin-Dependent, 7 35 0.019
417
P HYP599 Hypoparathyroidism, Familial Isolated 34 0.019
418
LNS003 Lens Disease 33 0.019
419
GLS004 Glossopharyngeal Neuralgia 33 0.019
420
DBT090 Diabetes and Deafness, Maternally Inherited 33 0.019
421
c GLY009 Glycogen Storage Disease Xv 33 0.019
422
EPD019 Epidural Neoplasm 33 0.019
423
c DNT021 Dent Disease 2 33 0.019
424
SCH068 Schwartz-Jampel Syndrome, Type 1 32 0.019
425
THR099 Third-Degree Atrioventricular Block 32 0.019
426
MTC028 Mitochondrial Cardiomyopathy 32 0.019
427
KDN013 Kidney Hypertrophy 31 0.019
428
P ACT080 Acute Pulmonary Heart Disease 31 0.019
429
IRS003 Iris Disease 31 0.019
430
c ATM068 Autoimmune Hypoparathyroidism 30 0.019
431
MDY006 Mody, Type Iv 30 0.019
432
c CTS034 Cutis Laxa, Autosomal Recessive Type 1 30 0.019
433
EHL060 Ehlers-Danlos Syndrome Due to Tenascin X Deficiency 29 0.019
434
c AST037 Asthma 1 29 0.019
435
P PHC014 Phocomelia 29 0.019
436
c AST039 Asthma 2 28 0.019
437
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.019
438
c FML250 Familial Progressive Cardiac Conduction Defect 28 0.019
439
c CRD198 Cardiomyopathy, Hypertrophic, 18 28 0.019
440
c CRD107 Cardiomyopathy, Dilated, 1r 27 0.019
441
c ATR038 Atrial Fibrillation, Familial, 3 27 0.019
442
c VNT028 Ventricular Septal Defect 1 27 0.019
443
TYP027 Type 1 Diabetes Mellitus 10 27 0.019
444
CRB031 Cerebral Arterial Disease 27 0.019
445
PST048 Postural Orthostatic Tachycardia Syndrome 27 0.019
446
c STR092 Striatal Degeneration, Autosomal Dominant 2 27 0.019
447
PCW002 Pcwh Syndrome 26 0.019
448
c FML294 Familial Short Qt Syndrome 26 0.019
449
SHP003 Shapiro Syndrome 26 0.019
450
ANG060 Angiopathy, Hereditary, with Nephropathy, Aneurysms, and Muscle Cramps 26 0.019
451
HYP711 Hypotonia, Ataxia, and Delayed Development Syndrome 26 0.019
452
c JRV002 Jervell and Lange-Nielsen Syndrome 2 26 0.019
453
c CNG404 Congenital Heart Defects, Multiple Types, 4 26 0.019
454
NSP003 Nasopharyngeal Disease 26 0.019
455
ARR037 Arrhythmogenic Right Ventricular Dysplasia 12 25 0.019
456
ARR038 Arrhythmogenic Right Ventricular Dysplasia 11 25 0.019
457
c VNT024 Ventricular Septal Defect 3 25 0.019
458
BRK012 Broken Heart Syndrome 25 0.019
459
SCN049 Second-Degree Atrioventricular Block 24 0.019
460
EYC003 Eye Accommodation Disease 24 0.019
461
MTC068 Mitochondrial Complex V Deficiency, Nuclear Type 2 24 0.019
462
c EMR012 Emery-Dreifuss Muscular Dystrophy 3, Ar 23 0.019
463
c VNT026 Ventricular Septal Defect 2 23 0.019
464
NTH002 Nathalie Syndrome 23 0.019
465
c SCK022 Sick Sinus Syndrome 3 22 0.019
466
c LFT017 Left Ventricular Noncompaction 8 22 0.019
467
CRB087 Cerebral Arteriosclerosis 21 0.019
468
MCL055 Mcleod Syndrome with or Without Chronic Granulomatous Disease 21 0.019
469
c CRD173 Cardiomyopathy, Dilated, 1nn 21 0.019
470
APN006 Apnea of Prematurity 21 0.019
471
CRD201 Cardiomyopathy, Dilated, 1c, with or Without Lvnc 20 0.019
472
c RNL016 Renal Infectious Disease 20 0.019
473
c BRG010 Brugada Syndrome 8 20 0.019
474
ARR041 Arrhythmogenic Right Ventricular Dysplasia, Familial, 13 20 0.019
475
HYP682 Hypertelorism, Teebi Type 19 0.019
476
VSC009 Vascular Skin Disease 19 0.019
477
c RNL034 Renal Cell Carcinoma 4 18 0.019
478
c BRG012 Brugada Syndrome 9 18 0.019
479
NN2002 Non 24 Hour Sleep Wake Disorder 18 0.019
480
ATN001 Autonomic Peripheral Neuropathy 17 0.019
481
PLM008 Pulmonary Subvalvular Stenosis 17 0.019
482
c ATR025 Atrial Fibrillation, Familial, 2 16 0.019
483
TBT001 Tabatznik Syndrome 16 0.019
484
HYD050 Hydrocephalus, Endocardial Fibroelastosis, and Cataracts 16 0.019
485
c HYP453 Hypertension, Essential 7 15 0.019
486
HRS003 Hirschsprung Disease Ganglioneuroblastoma 15 0.019
487
CLC053 Colchicine Poisoning 15 0.019
488
ARR036 Arrhythmogenic Right Ventricular Dysplasia 3 15 0.019
489
EPL095 Epilepsy with Myoclonic Absences 15 0.019
490
HRT029 Heart Tumor of the Child 15 0.019
491
WLL032 Woolly Hair, Hypotrichosis, Everted Lower Lip, and Outstanding Ears 15 0.019
492
CRD023 Cardiomyopathy Cataract Hip Spine Disease 15 0.019
493
SBR011 Subaortic Stenosis--Short Stature Syndrome 15 0.019
494
CTN032 Cutaneous Mastocytosis, Conductive Hearing Loss and Microtia 14 0.019
495
ECT023 Ectodermal Dysplasia, Hidrotic, Christianson-Fourie Type 13 0.019
496
THL008 Thalamic Degeneration, Symmetric Infantile 13 0.019
497
19P001 19p13.12 Microdeletion Syndrome 12 0.019
498
PLY088 Polyvalvular Heart Disease Syndrome 12 0.019
499
ARR005 Arrhythmogenic Right Ventricular Dysplasia/cardiomyopathy 2 12 0.019
500
CNG288 Congenital Absence of Upper Arm and Forearm with Hand Present 11 0.019
501
PLY127 Polyneuropathy-Intellectual Disability-Acromicria-Premature Menopause Syndrome 11 0.019
502
ARR006 Arrhythmogenic Right Ventricular Dysplasia/cardiomyopathy 3 10 0.019
503
PNC065 Pinched Nerve 10 0.019
504
ART033 Aortic Valves Stenosis of the Child 9 0.019
505
TRS022 Torsade De Pointes, Short-Coupled Variant 6 0.019
506
P BRS047 Breast Cancer 100 0.013
507
P CLR023 Colorectal Cancer 97 0.013
508
P LNG032 Lung Cancer 95 0.013
509
P ALZ034 Alzheimer Disease 92 0.013
510
P HPT023 Hepatocellular Carcinoma 92 0.013
511
P OBS005 Obesity 92 0.013
512
P PRS040 Prostate Cancer 90 0.013
513
P RHM011 Rheumatoid Arthritis 89 0.013
514
P PNC035 Pancreatic Cancer 87 0.013
515
P OST012 Osteoarthritis 83 0.013
516
CYS001 Cystic Fibrosis 83 0.013
517
MLR004 Malaria 83 0.013
518
P AST005 Asthma 82 0.013
519
HV1006 Hiv-1 80 0.013
520
P HNT016 Huntington Disease 80 0.013
521
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 78 0.013
522
GST053 Gastric Cancer 78 0.013
523
P MDL005 Medulloblastoma 77 0.013
524
P SCH015 Schizophrenia 77 0.013
525
HDG012 Hodgkin Lymphoma 77 0.013
526
P OVR042 Ovarian Cancer 76 0.013
527
ESP021 Esophageal Cancer 76 0.013
528
P HYP607 Hypercholesterolemia, Familial 76 0.013
529
c CHR090 Chronic Lymphocytic Leukemia 76 0.013
530
ULC004 Ulcerative Colitis 76 0.013
531
P ART022 Arthritis 75 0.013
532
P LVR013 Liver Disease 75 0.013
533
END057 Endometrial Cancer 75 0.013
534
CRH001 Crohn's Disease 75 0.013
535
INS024 Insulin-Like Growth Factor I 75 0.013
536
P RTN024 Retinoblastoma 74 0.013
537
c LKM061 Leukemia, Acute Myeloid 73 0.013
538
MYL009 Myelodysplastic Syndrome 73 0.013
539
c MCL042 Macular Degeneration, Age-Related, 1 73 0.013
540
c HPT073 Hepatitis C Virus 73 0.013
541
WLS001 Wilson Disease 72 0.013
542
PHN003 Phenylketonuria 72 0.013
543
P ALG002 Alagille Syndrome 72 0.013
544
MNT001 Mantle Cell Lymphoma 72 0.013
545
P PLM036 Pulmonary Fibrosis 71 0.013
546
P LKM002 Leukemia 71 0.013
547
SCK003 Sickle Cell Anemia 71 0.013
548
KRT004 Keratitis 71 0.013
549
MLT021 Multiple System Atrophy 70 0.013
550
P LGH007 Leigh Syndrome 70 0.013
551
P PRK057 Parkinson Disease, Late-Onset 70 0.013
552
P NRB001 Neuroblastoma 70 0.013
553
SQM013 Squamous Cell Carcinoma, Head and Neck 70 0.013
554
BRN028 Brain Cancer 70 0.013
555
SQM006 Squamous Cell Carcinoma 70 0.013
556
P ESS003 Essential Thrombocythemia 70 0.013
557
TBR010 Tuberculosis 70 0.013
558
CRZ001 Crouzon Syndrome 70 0.013
559
P ADN016 Adenocarcinoma 69 0.013
560
THY028 Thyroid Cancer 69 0.013
561
TST021 Testicular Germ Cell Tumor 69 0.013
562
c MLT136 Multiple Endocrine Neoplasia 1 69 0.013
563
P LYM118 Lymphoma 69 0.013
564
SVR004 Severe Combined Immunodeficiency 69 0.013
565
P HPT021 Hepatitis 69 0.013
566
ART016 Aortic Aneurysm 69 0.013
567
c HPT001 Hepatitis C 68 0.013
568
P GLB002 Glioblastoma 68 0.013
569
P PNM007 Pneumonia 68 0.013
570
P LKM068 Leukemia, Chronic Myeloid, Somatic 68 0.013
571
PSY004 Psychotic Disorder 67 0.013
572
PLM001 Pulmonary Tuberculosis 67 0.013
573
KPS004 Kaposi Sarcoma 67 0.013
574
P MYL005 Myelofibrosis 67 0.013
575
P TBR001 Tuberous Sclerosis 67 0.013
576
P CHR071 Charcot-Marie-Tooth Disease 67 0.013
577
P END044 Endometriosis 66 0.013
578
CRB037 Cerebral Palsy 66 0.013
579
EWN003 Ewing Sarcoma 66 0.013
580
OTT002 Otitis Media 66 0.013
581
URN008 Urinary Bladder Cancer 66 0.013
582
P MYL006 Myeloid Leukemia 66 0.013
583
ART005 Arteriovenous Malformation 66 0.013
584
DRM006 Dermatitis 66 0.013
585
OBS002 Obsessive-Compulsive Disorder 66 0.013
586
INC002 Inclusion Body Myositis 66 0.013
587
BRC012 Brucellosis 66 0.013
588
DWN001 Down Syndrome 66 0.013
589
ATP002 Atopy 66 0.013
590
SRC014 Sarcoma 66 0.013
591
P ATS007 Autism Spectrum Disorder 65 0.013
592
CRV047 Cervical Cancer, Somatic 65 0.013
593
P BCL006 B-Cell Lymphomas 65 0.013
594
P PLZ001 Pelizaeus-Merzbacher Disease 65 0.013
595
P DYS154 Dystonia 65 0.013
596
c BSL007 Basal Cell Carcinoma 65 0.013
597
DMN002 Dementia 65 0.013
598
P HRP006 Herpes Simplex 65 0.013
599
P AST007 Astrocytoma 65 0.013
600
P PLR004 Pleuropulmonary Blastoma 65 0.013
601
c HPT016 Hepatitis B 65 0.013
602
P AGM001 Agammaglobulinemia 64 0.013
603
P ART023 Arthropathy 64 0.013
604
P ORT004 Orthostatic Intolerance 64 0.013
605
HMT002 Hematologic Cancer 64 0.013
606
DFC004 Deficiency Anemia 64 0.013
607
BRN024 Bronchitis 64 0.013
608
P THR014 Thrombocytopenia 64 0.013
609
PSR001 Psoriatic Arthritis 64 0.013
610
P ANR002 Aniridia 64 0.013
611
P RBN001 Rubinstein-Taybi Syndrome 64 0.013
612
CHR066 Chronic Fatigue Syndrome 64 0.013
613
P OST002 Osteoporosis 64 0.013
614
LYM115 Lymphoma, Non-Hodgkin 63 0.013
615
P INF037 Inflammatory Bowel Disease 63 0.013
616
ATS001 Autistic Disorder 63 0.013
617
P HYP098 Hypereosinophilic Syndrome 63 0.013
618
P PRD008 Periodontitis 63 0.013
619
PLY125 Polycythemia Vera, Somatic 63 0.013
620
ALC007 Alcohol Dependence 63 0.013
621
P ALX003 Alexander Disease 63 0.013
622
LYM017 Lyme Disease 63 0.013
623
ALL003 Allergic Rhinitis 63 0.013
624
RNL101 Renal Cell Carcinoma, Papillary 63 0.013
625
OST085 Osteosarcoma, Somatic 63 0.013
626
GLB015 Glioblastoma Multiforme 63 0.013
627
PRT036 Peritonitis 63 0.013
628
PLM129 Pulmonary Disease, Chronic Obstructive 63 0.013
629
P EHL001 Ehlers-Danlos Syndrome 63 0.013
630
MLN008 Melanoma 62 0.013
631
P MCL013 Mucolipidosis Iv 62 0.013
632
P LNG064 Lung Cancer Susceptibility 3 62 0.013
633
P ADD001 Addison's Disease 62 0.013
634
P HML002 Hemolytic Anemia 62 0.013
635
P CRN015 Cornelia De Lange Syndrome 62 0.013
636
MXD005 Mixed Connective Tissue Disease 62 0.013
637
VSC011 Vasculitis 62 0.013
638
P PRS038 Personality Disorder 62 0.013
639
P ATP001 Atopic Dermatitis 62 0.013
640
GST092 Gastroesophageal Reflux 62 0.013
641
APH001 Aphthous Stomatitis 62 0.013
642
P DRM010 Dermatomyositis 62 0.013
643
GLC037 Glucocorticoid Resistance 62 0.013
644
P NRC002 Narcolepsy 62 0.013
645
P LYM026 Lymphoblastic Leukemia 62 0.013
646
SKN019 Skin Melanoma 62 0.013
647
P PRD006 Prader-Willi Syndrome 62 0.013
648
ACN011 Acne 62 0.013
649
P ALP009 Alopecia Areata 62 0.013
650
GNG013 Gingivitis 61 0.013
651
P LYM025 Lymphedema 61 0.013
652
P PSR002 Psoriasis 61 0.013
653
VNW001 Von Willebrand's Disease 61 0.013
654
P ASP006 Aspergillosis 61 0.013
655
P ESP024 Esophagitis 61 0.013
656
P IDP010 Idiopathic Generalized Epilepsy 61 0.013
657
P ADL010 Adult Respiratory Distress Syndrome 61 0.013
658
P HYP117 Hypertriglyceridemia 61 0.013
659
BRS051 Breast Disease 61 0.013
660
MTH009 Mouth Disease 61 0.013
661
PLM134 Pulmonary Fibrosis, Idiopathic 61 0.013
662
TYP007 Typhoid Fever 61 0.013
663
TTN003 Tetanus 61 0.013
664
MDD011 Mood Disorder 61 0.013
665
P HYP055 Hypoplastic Left Heart Syndrome 61 0.013
666
P PNC044 Pancreatitis 61 0.013
667
EYD002 Eye Disease 61 0.013
668
c ATM010 Autoimmune Hemolytic Anemia 61 0.013
669
P NPH009 Nephrolithiasis 60 0.013
670
INT146 Intervertebral Disc Disease 60 0.013
671
P TMP003 Temporal Arteritis 60 0.013
672
ACQ007 Acquired Immunodeficiency Syndrome 60 0.013
673
c EHL057 Ehlers-Danlos Syndrome, Type Iv 60 0.013
674
P FCL005 Focal Segmental Glomerulosclerosis 60 0.013
675
c CNG006 Congenital Hypothyroidism 60 0.013
676
P SNS014 Sinusitis 60 0.013
677
P INT068 Intestinal Disease 60 0.013
678
P PRT013 Portal Hypertension 60 0.013
679
CLT003 Colitis 60 0.013
680
TXC005 Toxic Shock Syndrome 60 0.013
681
P GLM045 Glioma 60 0.013
682
P GST049 Gastrointestinal System Cancer 60 0.013
683
PRM097 Primary Immunodeficiency Disease 60 0.013
684
PRD007 Periodontal Disease 60 0.013
685
c VRL010 Viral Hepatitis 60 0.013
686
LPM004 Lipoma 60 0.013
687
c ACT073 Acute Leukemia 60 0.013
688
FLL027 Fallopian Tube Carcinoma 60 0.013
689
P GLY013 Glycogen Storage Disease 60 0.013
690
c ADL017 Adult T-Cell Leukemia 60 0.013
691
P SPN052 Spondyloarthropathy 60 0.013
692
WLL001 Williams-Beuren Syndrome 60 0.013
693
MLG108 Malignant Melanoma, Somatic 60 0.013
694
P PNC025 Panic Disorder 60 0.013
695
P RHN004 Rhinitis 60 0.013
696
CRV038 Cervical Squamous Cell Carcinoma 60 0.013
697
GLB001 Gilbert Syndrome 60 0.013
698
c MNN043 Meningioma, Familial 59 0.013
699
P ORL007 Oral Cavity Cancer 59 0.013
700
KRT001 Keratoconjunctivitis Sicca 59 0.013
701
P HMN010 Hemangioma 59 0.013
702
ALC006 Alcoholic Hepatitis 59 0.013
703
OCL009 Ocular Cancer 59 0.013
704
c HPT003 Hepatitis a 59 0.013
705
P THR015 Thrombophilia 59 0.013
706
GST045 Gastroenteritis 59 0.013
707
P HRM001 Hermansky-Pudlak Syndrome 59 0.013
708
FTT001 Fatty Liver Disease 59 0.013
709
DPH001 Diphtheria 59 0.013
710
P GLL020 Gallbladder Disease 59 0.013
711
INT066 Interstitial Lung Disease 59 0.013
712
P INF032 Infertility 59 0.013
713
P INT001 Intrahepatic Cholestasis 59 0.013
714
P ALC004 Alcohol Abuse 59 0.013
715
P GLM007 Glomerulonephritis 59 0.013
716
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.013
717
DFF005 Diffuse Large B-Cell Lymphoma 59 0.013
718
c ESS001 Essential Tremor 59 0.013
719
CMM005 Common Cold 59 0.013
720
c EXD008 Exudative Vitreoretinopathy 1 59 0.013
721
MRB003 Morbid Obesity 59 0.013
722
MYL031 Myeloproliferative Neoplasm 58 0.013
723
P PLY018 Polycythemia 58 0.013
724
ALL006 Allergic Asthma 58 0.013
725
PRP030 Purpura 58 0.013
726
P CTS001 Cutis Laxa 58 0.013
727
LPD008 Lipid Metabolism Disorder 58 0.013
728
P SHR029 Short Syndrome 58 0.013
729
P HYP060 Hyperinsulinism 58 0.013
730
ETN001 Eating Disorder 58 0.013
731
P CTR002 Cataract 58 0.013
732
P MCR010 Microcephaly 58 0.013
733
MTR014 Motor Neuron Disease 58 0.013
734
P UVT001 Uveitis 58 0.013
735
P CMR001 Camurati-Engelmann Disease 58 0.013
736
P MTR004 Maturity-Onset Diabetes of the Young 58 0.013
737
RHM027 Rheumatic Disease 58 0.013
738
IRR002 Irritable Bowel Syndrome 58 0.013
739
MLG056 Malignant Hyperthermia 58 0.013
740
P BRS044 Breast Adenocarcinoma 58 0.013
741
P HYP069 Hyperparathyroidism 58 0.013
742
PNC034 Pancreas Disease 58 0.013
743
BNC003 Bone Cancer 58 0.013
744
SYN007 Synovitis 58 0.013
745
DBT087 Diabetes Insipidus, Neurohypophyseal 58 0.013
746
ING001 Inguinal Hernia 58 0.013
747
EMP007 Emphysema Due to Aat Deficiency 58 0.013
748
P THR003 Thoracic Aortic Aneurysm 57 0.013
749
PST028 Post-Traumatic Stress Disorder 57 0.013
750
KND001 Kindler Syndrome 57 0.013
751
P LRY044 Larynx Cancer 57 0.013
752
CTS003 Coats Disease 57 0.013
753
ABL002 Ablepharon-Macrostomia Syndrome 57 0.013
754
P HYP040 Hypospadias 57 0.013
755
EMB004 Embryonal Carcinoma 57 0.013
756
RHB003 Rhabdomyosarcoma 57 0.013
757
c FML108 Familial Breast Cancer 57 0.013
758
TRG002 Trigeminal Neuralgia 57 0.013
759
CHY002 Chylomicron Retention Disease 57 0.013
760
CHL067 Cholecystitis 57 0.013
761
c CWD006 Cowden Syndrome 1 57 0.013
762
CNS004 Constipation 57 0.013
763
ORL015 Oral Squamous Cell Carcinoma 57 0.013
764
URT039 Urticaria 57 0.013
765
c GLY060 Glycogen Storage Disease Ia 57 0.013
766
SFT003 Soft Tissue Sarcoma 57 0.013
767
CRT016 Carotid Artery Disease 57 0.013
768
PNC033 Pancreas Adenocarcinoma 57 0.013
769
MSC077 Muscle Eye Brain Disease 57 0.013
770
GST033 Gestational Diabetes 57 0.013
771
c ACT027 Acute Pancreatitis 57 0.013
772
c ACT210 Acute Respiratory Distress Syndrome 57 0.013
773
P HMR003 Hemorrhagic Disease 57 0.013
774
EXF001 Exfoliation Syndrome 57 0.013
775
UTR039 Uterine Fibroid 57 0.013
776
WST001 West Syndrome 57 0.013
777
c MCR115 Microvascular Complications of Diabetes 5 57 0.013
778
P INT143 Interstitial Cystitis 57 0.013
779
P INT070 Intestinal Obstruction 57 0.013
780
STR026 Star Syndrome 57 0.013
781
ETH011 Ethylmalonic Encephalopathy 56 0.013
782
MCR264 Mcardle Disease 56 0.013
783
c PRC016 Pre-Eclampsia 56 0.013
784
ORL011 Oral Cancer 56 0.013
785
P MST009 Mastocytosis 56 0.013
786
PLY023 Polycystic Liver Disease 56 0.013
787
RTN017 Retinal Detachment 56 0.013
788
HRP004 Herpes Zoster 56 0.013
789
MLN054 Melanocytic Nevus Syndrome, Congenital, Somatic 56 0.013
790
P SML001 Small Cell Carcinoma 56 0.013
791
P DST002 Distal Arthrogryposis 56 0.013
792
P FRS003 Fraser Syndrome 56 0.013
793
BRN002 Bronchiolitis 56 0.013
794
INT002 Intermittent Claudication 56 0.013
795
P MLT074 Multiple Endocrine Neoplasia 56 0.013
796
PHR003 Pharyngitis 56 0.013
797
P LYM033 Lymphoproliferative Syndrome 56 0.013
798
P OLG002 Oligodendroglioma 56 0.013
799
P MYP006 Myopia 56 0.013
800
NRN004 Neuroendocrine Tumor 56 0.013
801
CLR003 Clear Cell Adenocarcinoma 56 0.013
802
GST023 Gastric Ulcer 56 0.013
803
IDP011 Idiopathic Interstitial Pneumonia 56 0.013
804
PRS047 Prostatitis 56 0.013
805
P OVR049 Ovarian Disease 56 0.013
806
GST050 Gastrointestinal System Disease 56 0.013
807
HPT019 Hepatic Encephalopathy 56 0.013
808
P HYP050 Hyperinsulinemic Hypoglycemia 56 0.013
809
VRL011 Viral Infectious Disease 55 0.013
810
c HRD002 Hereditary Angioedema 55 0.013
811
JNT002 Joint Disorders 55 0.013
812
DBT010 Diabetic Neuropathy 55 0.013
813
PRR007 Perry Syndrome 55 0.013
814
THR004 Thrombocytosis 55 0.013
815
PLM034 Pulmonary Emphysema 55 0.013
816
P SCL018 Scoliosis 55 0.013
817
GLC003 Glucose Intolerance 55 0.013
818
P LPD010 Lipodystrophy 55 0.013
819
P FNC043 Fanconi Anemia, Complementation Group E 55 0.013
820
MLN007 Male Infertility 55 0.013
821
SPN027 Spinal Stenosis 55 0.013
822
URN010 Urinary Tract Obstruction 55 0.013
823
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.013
824
ERY003 Erythema Multiforme 55 0.013
825
MCS002 Mucositis 55 0.013
826
PLS007 Plasmodium Falciparum Malaria 55 0.013
827
P RTN016 Retinal Degeneration 54 0.013
828
P TRM003 Tremor 54 0.013
829
P HYP345 Hyper-Ige Recurrent Infection Syndrome 54 0.013
830
c THR092 Thrombophilia Due to Thrombin Defect 54 0.013
831
PLM012 Pulmonary Sarcoidosis 54 0.013
832
HDC001 Headache 54 0.013
833
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 54 0.013
834
RCT018 Rectal Neoplasm 54 0.013
835
CRN183 Carnitine Palmitoyltransferase Ii Deficiency 54 0.013
836
P MMB011 Membranous Nephropathy 54 0.013
837
CHN016 Cohen Syndrome 54 0.013
838
c THR082 Thrombophilia Due to Activated Protein C Resistance 54 0.013
839
VSC002 Vascular Dementia 54 0.013
840
SBS003 Substance Abuse 54 0.013
841
c PRM126 Primary Peritoneal Carcinoma 54 0.013
842
KLP010 Klippel-Trenaunay-Weber Syndrome 54 0.013
843
MCN017 Meconium Ileus 54 0.013
844
CMP010 Complex Regional Pain Syndrome 54 0.013
845
LMY002 Leiomyoma 54 0.013
846
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 54 0.013
847
ESP023 Esophageal Disease 54 0.013
848
PLM010 Pulmonary Edema 54 0.013
849
c HPT007 Hepatitis E 54 0.013
850
PLN006 Poland Syndrome 54 0.013
851
P OCL002 Oculocutaneous Albinism 54 0.013
852
VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 54 0.013
853
P MYP101 Myopathy, Centronuclear 54 0.013
854
P INT030 Intracranial Aneurysm 54 0.013
855
P ECL001 Eclampsia 54 0.013
856
P BRN009 Burning Mouth Syndrome 54 0.013
857
PLV003 Pelvic Inflammatory Disease 54 0.013
858
PST046 Post-Transplant Lymphoproliferative Disease 54 0.013
859
SML033 Small Cell Cancer of the Lung, Somatic 54 0.013
860
P VNS003 Venous Insufficiency 54 0.013
861
RST001 Restless Legs Syndrome 54 0.013
862
CRV040 Cervix Carcinoma 53 0.013
863
P MTC069 Mitochondrial Disorders 53 0.013
864
C3D001 C3 Deficiency 53 0.013
865
DMY004 Demyelinating Disease 53 0.013
866
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 53 0.013
867
GST027 Gastric Lymphoma 53 0.013
868
FRB001 Farber Lipogranulomatosis 53 0.013
869
CPR001 Coproporphyria 53 0.013
870
FDL002 Food Allergy 53 0.013
871
PRT014 Protein S Deficiency 53 0.013
872
PYR010 Peyronie's Disease 53 0.013
873
P LTR001 Lateral Sclerosis 53 0.013
874
P LPC002 Lip Cancer 53 0.013
875
P EXP004 Exophthalmos 53 0.013
876
PNM008 Pneumothorax 53 0.013
877
SCT005 Scott Syndrome 53 0.013
878
ANG020 Angiosarcoma 53 0.013
879
c INS002 in Situ Carcinoma 53 0.013
880
P SYP003 Syphilis 53 0.013
881
RTN018 Retinal Disease 53 0.013
882
P DBT005 Diabetes Insipidus 53 0.013
883
THR016 Thrombophlebitis 53 0.013
884
P CNT005 Central Nervous System Lymphoma 53 0.013
885
PLS006 Plasmodium Vivax Malaria 53 0.013
886
LYM019 Lymphosarcoma 53 0.013
887
NRF007 Neurofibroma 53 0.013
888
HMR039 Hemorrhage, Intracerebral 53 0.013
889
c ALZ036 Alzheimer Disease, Type 3 53 0.013
890
PRV006 Pervasive Developmental Disorder 53 0.013
891
BLT006 Bilateral Breast Cancer 53 0.013
892
P CYS018 Cystitis 52 0.013
893
TLN003 Telangiectasis 52 0.013
894
DSS008 Disease of Mental Health 52 0.013
895
RSC001 Rosacea 52 0.013
896
P SML016 Small Intestine Cancer 52 0.013
897
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.013
898
LYS002 Lysosomal Storage Disease 52 0.013
899
TTH006 Tooth Disease 52 0.013
900
P NNT009 Neonatal Diabetes Mellitus 52 0.013
901
BLM002 Bulimia Nervosa 52 0.013
902
BRN004 Brain Edema 52 0.013
903
TRM010 Traumatic Brain Injury 52 0.013
904
BLR006 Biliary Tract Disease 52 0.013
905
PRT058 Pure Autonomic Failure 52 0.013
906
P ANG015 Angioedema 52 0.013
907
CYT008 Cytomegalovirus Infection 52 0.013
908
c HPT015 Hepatitis D 52 0.013
909
c INF023 Inflammatory Breast Carcinoma 52 0.013
910
c ALZ037 Alzheimer Disease-2 52 0.013
911
GST040 Gastric Adenocarcinoma 52 0.013
912
HMG005 Hemoglobinopathy 52 0.013
913
P MGR003 Migraine with Aura 52 0.013
914
PRT011 Protein C Deficiency 52 0.013
915
DGN001 Degenerative Disc Disease 52 0.013
916
c OPT055 Optic Atrophy Plus Syndrome 52 0.013
917
KRT009 Keratosis 52 0.013
918
CRH005 Crohn's Colitis 52 0.013
919
LYM024 Lymphatic System Disease 52 0.013
920
OPT006 Optic Nerve Disease 52 0.013
921
MYC002 Mycobacterium Avium Complex Disease 52 0.013
922
PRS042 Prostate Disease 52 0.013
923
CRC006 Carcinoid Syndrome 52 0.013
924
MYM001 Myoma 52 0.013
925
NRP015 Neuropathy, Congenital Hypomyelinating 52 0.013
926
BLR001 Biliary Atresia 52 0.013
927
DBT004 Diabetic Polyneuropathy 52 0.013
928
c PRM012 Primary Polycythemia 52 0.013
929
MSS001 Masa Syndrome 52 0.013
930
c PRK031 Parkinson Disease 1 51 0.013
931
BLD044 Bladder Disease 51 0.013
932
PHL006 Phelan-Mcdermid Syndrome 51 0.013
933
P ERY008 Erythromelalgia 51 0.013
934
BRN038 Bronchial Disease 51 0.013
935
c INF071 Inflammatory Bowel Disease 1 51 0.013
936
P PTS002 Ptosis 51 0.013
937
ART002 Arts Syndrome 51 0.013
938
DBT062 Diabetic Foot Ulcers 51 0.013
939
TXC002 Toxic Encephalopathy 51 0.013
940
P STR020 Strabismus 51 0.013
941
PLR022 Pleural Disease 51 0.013
942
DRG011 Drug Addiction 51 0.013
943
P CPL006 Capillary Hemangioma 51 0.013
944
CHC001 Chickenpox 51 0.013
945
PNN001 Panniculitis 51 0.013
946
VSC006 Vascular Cancer 51 0.013
947
P LMB006 Limb-Girdle Muscular Dystrophy 51 0.013
948
SRS001 Serous Cystadenocarcinoma 51 0.013
949
ACT008 Actinic Keratosis 51 0.013
950
c FML053 Familial Colorectal Cancer 51 0.013
951
PTH002 Pathological Gambling 51 0.013
952
CLR109 Colorectal Adenocarcinoma 51 0.013
953
GNR004 Generalized Anxiety Disorder 51 0.013
954
P HRD018 Hair Disease 51 0.013
955
KLD001 Keloids 51 0.013
956
CLL003 Cellulitis 51 0.013
957
P PRC031 Preeclampsia/eclampsia 1 51 0.013
958
IMM136 Immune System Disease 51 0.013
959
CRS005 Crest Syndrome 51 0.013
960
SCK005 Sickle Cell Disease 51 0.013
961
SPN041 Spinal Cord Disease 51 0.013
962
SPN051 Spondylitis 51 0.013
963
DSS009 Disseminated Intravascular Coagulation 51 0.013
964
HMP005 Hemiplegia 51 0.013
965
BNM001 Bone Marrow Cancer 51 0.013
966
CLN019 Colonic Disease 51 0.013
967
P SMP003 Simpson-Golabi-Behmel Syndrome 51 0.013
968
STM006 Stomach Disease 50 0.013
969
P CTN015 Cutaneous T Cell Lymphoma 50 0.013
970
c GLY019 Glycogen Storage Disease Iiia 50 0.013
971
NDL013 Nodular Regenerative Hyperplasia 50 0.013
972
P HYP014 Hyperuricemia 50 0.013
973
GRW007 Growth Hormone Deficiency 50 0.013
974
P HYP065 Hyperaldosteronism 50 0.013
975
ESN005 Eosinophilic Gastroenteritis 50 0.013
976
CLN015 Colon Adenocarcinoma 50 0.013
977
DYS014 Dyspepsia 50 0.013
978
FCL012 Facial Paralysis 50 0.013
979
P RST002 Restrictive Cardiomyopathy 50 0.013
980
HND003 Hand-Foot-Uterus Syndrome 50 0.013
981
BRS099 Breast Ductal Carcinoma 50 0.013
982
CLC006 Calcinosis 50 0.013
983
SMT006 Somatoform Disorder 50 0.013
984
FML038 Female Reproductive Organ Cancer 50 0.013
985
RDC002 Radiculopathy 50 0.013
986
MST017 Mast Cell Disease 50 0.013
987
BNF002 Bone Fracture 50 0.013
988
MCN001 Mucinous Adenocarcinoma 50 0.013
989
FML037 Female Breast Cancer 50 0.013
990
P CHR345 Chronic Pain 50 0.013
991
c ACT068 Acute Cystitis 50 0.013
992
RSS002 Roussy-Levy Syndrome 50 0.013
993
STM007 Stomatitis 50 0.013
994
c LYM107 Lymphoproliferative Syndrome 2 50 0.013
995
OPT003 Opiate Dependence 50 0.013
996
NNL002 Nonalcoholic Steatohepatitis 50 0.013
997
DRY001 Dry Eye Syndrome 50 0.013
998
P CLL015 Collagen Disease 50 0.013
999
HMN014 Human Immunodeficiency Virus Infectious Disease 50 0.013
1000
RHM028 Rheumatic Heart Disease 50 0.013
1001
P PNV001 Panuveitis 50 0.013
1002
THR013 Thoracic Outlet Syndrome 50 0.013
1003
INT075 Intracranial Hypertension 50 0.013
1004
c ACT134 Acute Liver Failure 50 0.013
1005
HLL004 Hellp Syndrome 50 0.013
1006
OST016 Osteochondrosis 50 0.013
1007
TMP001 Temporal Lobe Epilepsy 50 0.013
1008
OVR063 Overnutrition 50 0.013
1009
ANG054 Angina Pectoris 50 0.013
1010
STR081 Stormorken Syndrome 49 0.013
1011
END035 Endocrine Gland Cancer 49 0.013
1012
RTN015 Retinal Cancer 49 0.013
1013
c HRM005 Hermansky-Pudlak Syndrome 1 49 0.013
1014
BRX001 Bruxism 49 0.013
1015
P OPN001 Open-Angle Glaucoma 49 0.013
1016
MVM001 Movement Disease 49 0.013
1017
LPD009 Lipid Storage Disease 49 0.013
1018
MSC072 Muscle Cancer 49 0.013
1019
c SCN036 Secondary Progressive Multiple Sclerosis 49 0.013
1020
MSC006 Muscle Glycogenosis 49 0.013
1021
SRT004 Serotonin Syndrome 49 0.013
1022
c DYS166 Dysautonomia, Familial 49 0.013
1023
END021 Endomyocardial Fibrosis 49 0.013
1024
PST021 Postpartum Depression 49 0.013
1025
P MTH008 Methylmalonic Acidemia 49 0.013
1026
c PRM226 Primary Central Nervous System Lymphoma 49 0.013
1027
GLM004 Gliomatosis Cerebri 49 0.013
1028
c SVR005 Severe Pre-Eclampsia 49 0.013
1029
c INF067 Inflammatory Bowel Disease 10 49 0.013
1030
INN002 Inner Ear Disease 49 0.013
1031
ALC009 Alcoholic Liver Cirrhosis 49 0.013
1032
SLD003 Sialadenitis 49 0.013
1033
NCT008 Nicotine Dependence, Protection Against 49 0.013
1034
c ALM001 Al Amyloidosis 49 0.013
1035
c INH020 Inherited Metabolic Disorder 49 0.013
1036
BCL002 B Cell Deficiency 49 0.013
1037
PLR001 Pleural Tuberculosis 49 0.013
1038
c DWL002 Dowling-Degos Disease 1 49 0.013
1039
PRT018 Portal Vein Thrombosis 49 0.013
1040
CCN001 Cocaine Dependence 49 0.013
1041
MLL012 Miller Syndrome 49 0.013
1042
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.013
1043
HYP141 Hyperphenylalaninemia 49 0.013
1044
NNN026 Noonan Syndrome with Multiple Lentigines 48 0.013
1045