Search results for "arrhythmia"

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

2420 hits were found for 'arrhythmia'

# Family MCID Name MIFTS Score
1
CRD054 Cardiac Arrhythmia, Ankyrin-B-Related 22 3.551
2
PHC009 Phocomelia Ectrodactyly Deafness Sinus Arrhythmia 5 2.918
3
PHC016 Phocomelia-Ectrodactyly, Ear Malformation, Deafness, and Sinus Arrhythmia 15 2.913
4
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 32 2.897
5
c CRD099 Cardiomyopathy, Dilated, 1e 42 2.891
6
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 2.329
7
WLF001 Wolff-Parkinson-White Syndrome 57 2.103
8
SNT004 Sinoatrial Node Dysfunction and Deafness 27 2.099
9
SDD004 Sudden Arrhythmia Death Syndrome 15 2.099
10
NTR041 N-Terminal Acetyltransferase Deficiency 32 2.044
11
c ATS332 Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2x 15 2.044
12
P CRD011 Cardiomyopathy 67 0.115
13
P ATR011 Atrial Fibrillation 64 0.110
14
P HRT032 Heart Disease 76 0.104
15
P MYC007 Myocardial Infarction 79 0.104
16
c FML001 Familial Atrial Fibrillation 59 0.093
17
SDD007 Sudden Cardiac Death 46 0.093
18
c VNT013 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1 49 0.085
19
c CRN175 Coronary Heart Disease 4 21 0.084
20
P CRD132 Cardiac Conduction Defect 40 0.082
21
c CRN172 Coronary Heart Disease 3 21 0.081
22
VNT011 Ventricular Fibrillation, Familial, 1 43 0.077
23
CRD119 Cardiac Arrest 63 0.075
24
SYN036 Syncope 47 0.074
25
c ACT075 Acute Myocardial Infarction 60 0.070
26
P BRG001 Brugada Syndrome 59 0.070
27
ATR060 Atrial Standstill, Digenic 53 0.069
28
SNG003 Single Ventricular Heart 24 0.069
29
c DLT002 Dilated Cardiomyopathy 75 0.067
30
CNG034 Congestive Heart Failure 71 0.067
31
ISC004 Ischemia 59 0.065
32
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 58 0.065
33
P CRN178 Coronary Heart Disease 6 24 0.065
34
P CRN211 Coronary Artery Disease 75 0.063
35
c CRN174 Coronary Heart Disease 2 22 0.062
36
P SCK002 Sick Sinus Syndrome 50 0.059
37
P PRX010 Paroxysmal Ventricular Fibrillation 39 0.059
38
ISC006 Ischemic Heart Disease 68 0.056
39
CRD003 Cardiac Sarcoidosis 43 0.056
40
c CRN214 Coronary Heart Disease 5 23 0.054
41
HYP005 Hypokalemia 51 0.050
42
P MYT002 Myotonic Dystrophy 47 0.050
43
FNT004 Fainting 33 0.050
44
P MSC005 Muscular Dystrophy 64 0.049
45
ATR024 Atrial Fibrillation and Stroke 22 0.049
46
c LNG044 Long Qt Syndrome 1 67 0.047
47
P MYC008 Myocarditis 54 0.047
48
PRP027 Peripheral Vascular Disease 69 0.045
49
PRN021 Paranasal Sinus Disease 50 0.045
50
NSL022 Nasal Cavity Disease 42 0.045
51
ART111 Artery Disease 57 0.043
52
TTR001 Tetralogy of Fallot 71 0.040
53
P MYP004 Myopathy 67 0.040
54
ART021 Arteriosclerosis 59 0.040
55
ANR040 Aneurysm 57 0.040
56
SYS003 Systolic Heart Failure 43 0.040
57
c MYC058 Myocardial Infarction 2 29 0.040
58
P EPL164 Epilepsy 66 0.038
59
P SLP006 Sleep Apnea 61 0.038
60
P NRP001 Neuropathy 60 0.038
61
P AND016 Andersen Syndrome 58 0.038
62
CRN030 Coronary Stenosis 50 0.038
63
HYP006 Hypertensive Heart Disease 50 0.038
64
ATR057 Atrioventricular Block 49 0.038
65
TRN044 Transposition of the Great Arteries 47 0.038
66
SKN023 Skin Tag 46 0.038
67
ATN004 Autonomic Neuropathy 44 0.038
68
HRT012 Heart Valve Disease 41 0.038
69
STR067 Stroke, Ischemic 77 0.036
70
P CRD194 Cardiomyopathy, Familial Hypertrophic 64 0.036
71
RSP006 Respiratory System Disease 62 0.036
72
SLP005 Sleep Disorder 53 0.036
73
VND001 Vein Disease 52 0.036
74
ATN002 Autonomic Nervous System Disease 47 0.036
75
OBS061 Obstructive Sleep Apnea 66 0.033
76
HYP056 Hypoglycemia 61 0.033
77
NRM005 Neuromuscular Disease 57 0.033
78
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 55 0.033
79
P SPS003 Spastic Diplegia 53 0.033
80
P MSC033 Muscle Disorders 52 0.033
81
P LFT003 Left Ventricular Noncompaction 49 0.033
82
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.033
83
c SHR030 Short Qt Syndrome 43 0.033
84
DBT002 Diabetic Autonomic Neuropathy 42 0.033
85
ATR055 Atrial Septal Aneurysm 24 0.033
86
c CRN173 Coronary Heart Disease 8 20 0.033
87
DCH001 Duchenne Muscular Dystrophy 80 0.030
88
P RTT002 Rett Syndrome 78 0.030
89
FBR012 Fabry Disease 69 0.030
90
c HYP595 Hypertension, Essential 69 0.030
91
VSC007 Vascular Disease 67 0.030
92
c CHR089 Chronic Kidney Failure 66 0.030
93
c MYT021 Myotonic Dystrophy 1 62 0.030
94
P ENC018 Encephalopathy 59 0.030
95
P TMT001 Timothy Syndrome 56 0.030
96
P HYP076 Hyperthyroidism 56 0.030
97
INT007 Intermediate Coronary Syndrome 52 0.030
98
END030 End Stage Renal Failure 52 0.030
99
P MSC003 Muscular Atrophy 51 0.030
100
CSY001 C Syndrome 49 0.030
101
c LNG047 Long Qt Syndrome 2 49 0.030
102
CRD137 Cardiogenic Shock 46 0.030
103
RGH001 Right Bundle Branch Block 43 0.030
104
c BRG005 Brugada Syndrome 1 42 0.030
105
CRB009 Cerebritis 38 0.030
106
MSC004 Muscle Tissue Disease 36 0.030
107
STR037 Stress Cardiomyopathy 36 0.030
108
P HRT017 Heart Tumor 35 0.030
109
P LNG092 Long Qt Syndrome-3 35 0.030
110
c LNG053 Long Qt Syndrome 9 33 0.030
111
c LNG051 Long Qt Syndrome 6 31 0.030
112
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 29 0.030
113
c BRG003 Brugada Syndrome 3 26 0.030
114
c CRN177 Coronary Heart Disease 7 22 0.030
115
HSB001 His Bundle Tachycardia 22 0.030
116
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.027
117
BCK001 Becker Muscular Dystrophy 68 0.027
118
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.027
119
P RFS001 Refsum Disease 62 0.027
120
ATH003 Atherosclerosis 62 0.027
121
P BPL003 Bipolar Disorder 62 0.027
122
CHG001 Chagas Disease 62 0.027
123
P SDD001 Sudden Infant Death Syndrome 61 0.027
124
c CNT035 Central Nervous System Disease 59 0.027
125
P MSC007 Muscle Hypertrophy 59 0.027
126
ADM013 Adamantinoma of Long Bones 59 0.027
127
P SYS005 Systemic Scleroderma 58 0.027
128
ART017 Aortic Disease 58 0.027
129
P SZR006 Seizure Disorder 57 0.027
130
CND002 Conduct Disorder 56 0.027
131
c ART101 Aortic Valve Disease 2 55 0.027
132
URN009 Urinary System Disease 53 0.027
133
ADL002 Adult Syndrome 53 0.027
134
BRT005 Barth Syndrome 53 0.027
135
P JRV003 Jervell and Lange-Nielsen Syndrome 52 0.027
136
P URF003 Urofacial Syndrome 1 52 0.027
137
BRN106 Burns 52 0.027
138
PRC012 Pericardial Effusion 50 0.027
139
HRT007 Heart Cancer 50 0.027
140
ADR038 Adermatoglyphia 48 0.027
141
CRD118 Cardiovascular Cancer 47 0.027
142
P THY054 Thyrotoxic Periodic Paralysis 47 0.027
143
GLC008 Glucose Metabolism Disease 47 0.027
144
ATN005 Autonomic Dysfunction 45 0.027
145
FDB001 Foodborne Botulism 45 0.027
146
c LNG050 Long Qt Syndrome 5 43 0.027
147
HRT008 Heart Conduction Disease 43 0.027
148
PRM025 Primary Bacterial Infectious Disease 43 0.027
149
HYP017 Hypophosphatemia 42 0.027
150
c FML191 Familial Long Qt Syndrome 41 0.027
151
PRP009 Peripartum Cardiomyopathy 41 0.027
152
c PRG106 Progressive Muscular Dystrophy 41 0.027
153
c CRD093 Cardiomyopathy, Dilated, 1a 38 0.027
154
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 38 0.027
155
IMP003 Impaired Renal Function Disease 37 0.027
156
INF013 Inferior Myocardial Infarction 37 0.027
157
c BRG006 Brugada Syndrome 2 33 0.027
158
GNT019 Giant Cell Myocarditis 31 0.027
159
c LNG056 Long Qt Syndrome 12 29 0.027
160
ARR030 Arrhythmogenic Right Ventricular Dysplasia 2 29 0.027
161
CNT017 Central Nervous System Origin Vertigo 28 0.027
162
c BRG004 Brugada Syndrome 4 22 0.027
163
c CRN176 Coronary Heart Disease 9 20 0.027
164
c ADL079 Adult Heart Tumor 19 0.027
165
P PLM037 Pulmonary Hypertension 79 0.023
166
P NRV007 Nervous System Disease 71 0.023
167
P RSP003 Respiratory Failure 70 0.023
168
KWS002 Kawasaki Disease 70 0.023
169
ANX002 Anxiety Disorder 69 0.023
170
CST001 Costello Syndrome 69 0.023
171
SKN016 Skin Disease 68 0.023
172
P KDN017 Kidney Cancer 67 0.023
173
ACR007 Acromegaly 65 0.023
174
TBR024 Tuberous Sclerosis-1 65 0.023
175
c SPN225 Spondyloarthropathy 1 63 0.023
176
LNG099 Lung Disease 62 0.023
177
SPN186 Spinal Cord Injury 62 0.023
178
c GLY008 Glycogen Storage Disease Ii 61 0.023
179
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.023
180
P OCL013 Oculodentodigital Dysplasia 59 0.023
181
CHL071 Child Syndrome 58 0.023
182
P EXN002 Exanthem 57 0.023
183
c MSC124 Muscular Dystrophy, Congenital 57 0.023
184
WLL006 Wells Syndrome 56 0.023
185
FCL014 Focal Epilepsy 56 0.023
186
HYP266 Hypoxia 55 0.023
187
P HYP192 Hypocalcemia, Autosomal Dominant 55 0.023
188
c PND001 Pain Disorder 55 0.023
189
MNT002 Mental Depression 54 0.023
190
P PLY019 Polyneuropathy 54 0.023
191
KDS001 Kid Syndrome 53 0.023
192
CPT004 Cpt Deficiency, Hepatic, Type Ii 52 0.023
193
NSD001 Nose Disease 52 0.023
194
P PLY041 Polymyositis 51 0.023
195
LRN003 Learning Disability 51 0.023
196
c EHL055 Ehlers-Danlos Syndrome, Type Iii 50 0.023
197
DBT084 Diabetes Mellitus, Ketosis-Prone 50 0.023
198
PRP021 Peripheral Nervous System Neoplasm 50 0.023
199
c MCR113 Microvascular Complications of Diabetes 3 49 0.023
200
P RNL015 Renal Hypertension 47 0.023
201
CCN002 Cocaine Abuse 47 0.023
202
ACR041 Acromelic Frontonasal Dysostosis 46 0.023
203
CRB004 Cerebral Artery Occlusion 46 0.023
204
P PLM040 Pulmonary Valve Disease 45 0.023
205
AYM001 Ayme-Gripp Syndrome 45 0.023
206
GDS001 Good Syndrome 45 0.023
207
MYC005 Myocardial Stunning 44 0.023
208
c CNT015 Central Sleep Apnea 44 0.023
209
BRT030 Birth Defects 43 0.023
210
c ACT076 Acute Myocarditis 42 0.023
211
CNV002 Conversion Disorder 42 0.023
212
CRN041 Carnitine-Acylcarnitine Translocase Deficiency 42 0.023
213
SPC003 Specific Developmental Disorder 40 0.023
214
RDN001 Reading Disorder 39 0.023
215
GST007 Gastric Dilatation 39 0.023
216
c BRG007 Brugada Syndrome 5 38 0.023
217
c BRN108 Branchiootic Syndrome 1 36 0.023
218
SNT005 Sinoatrial Node Disease 35 0.023
219
CPL011 Capillary Malformations, Congenital, 1, Somatic, Mosaic 35 0.023
220
INT084 Intrinsic Cardiomyopathy 35 0.023
221
MYT003 Myotonic Disease 34 0.023
222
SBV001 Subvalvular Aortic Stenosis 31 0.023
223
c CRD199 Cardiomyopathy, Hypertrophic 6 31 0.023
224
ARR026 Arrhythmogenic Right Ventricular Dysplasia 1 29 0.023
225
c DBT040 Diabetes Mellitus, Insulin-Dependent, 2 29 0.023
226
ARR040 Arrhythmogenic Right Ventricular Dysplasia 10 28 0.023
227
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 28 0.023
228
c LNG057 Long Qt Syndrome 13 27 0.023
229
c BRG009 Brugada Syndrome 7 25 0.023
230
c DBT082 Diabetes Mellitus, Insulin-Dependent, 12 24 0.023
231
MTC068 Mitochondrial Complex V Deficiency, Nuclear Type 2 24 0.023
232
CPT005 Cpt Ii Deficiency, Lethal Neonatal 24 0.023
233
c BRG008 Brugada Syndrome 6 24 0.023
234
MND006 Mondor Disease 21 0.023
235
c DBT056 Diabetes Mellitus, Insulin-Dependent, 4 21 0.023
236
c ATR074 Atrial Standstill 2 20 0.023
237
c LNG093 Long Qt Syndrome-11 19 0.023
238
MYT026 Myotonia Atrophica 19 0.023
239
ATR076 Atrophic Muscular Disease 18 0.023
240
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.019
241
P RNL014 Renal Cell Carcinoma 81 0.019
242
P MLT019 Multiple Myeloma 80 0.019
243
c AMY091 Amyotrophic Lateral Sclerosis 1 78 0.019
244
CRH001 Crohn's Disease 76 0.019
245
ULC004 Ulcerative Colitis 75 0.019
246
P INF038 Influenza 74 0.019
247
MRF001 Marfan Syndrome 73 0.019
248
P WSK001 Wiskott-Aldrich Syndrome 72 0.019
249
P HMC003 Hemochromatosis 72 0.019
250
P HRD008 Hereditary Hemorrhagic Telangiectasia 71 0.019
251
VNH007 Von Hippel-Lindau Syndrome 69 0.019
252
P DMN001 Diamond-Blackfan Anemia 68 0.019
253
P DRV001 Dravet Syndrome 68 0.019
254
PCK002 Pick Disease 67 0.019
255
P MYL006 Myeloid Leukemia 67 0.019
256
P NNN008 Noonan Syndrome 1 67 0.019
257
LVR012 Liver Cirrhosis 67 0.019
258
CNT098 Central Core Disease 66 0.019
259
P LKM068 Leukemia, Chronic Myeloid, Somatic 66 0.019
260
P MNN013 Meningitis 65 0.019
261
P HYP086 Hypothyroidism 65 0.019
262
c MLT024 Multiple Endocrine Neoplasia Iia 65 0.019
263
P AMY004 Amyloidosis 64 0.019
264
P FML161 Familial Mediterranean Fever, Ar 63 0.019
265
P SPN046 Spinal Muscular Atrophy 63 0.019
266
LPT001 Leptospirosis 63 0.019
267
LYM017 Lyme Disease 63 0.019
268
P HLP001 Holoprosencephaly 62 0.019
269
P NRV006 Nervous System Cancer 62 0.019
270
WGN006 Wegener Granulomatosis 62 0.019
271
P DNT015 Dent Disease 61 0.019
272
P THL005 Thalassemia 61 0.019
273
P GRV001 Graves' Disease 61 0.019
274
CNN005 Connective Tissue Disease 61 0.019
275
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 61 0.019
276
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 60 0.019
277
P RCK004 Rickets 59 0.019
278
c LCL006 Localized Scleroderma 59 0.019
279
RBR001 Roberts Syndrome 59 0.019
280
P MTR012 Mitral Valve Disease 59 0.019
281
LGN002 Legionellosis 59 0.019
282
P GT001 Gout 58 0.019
283
PRP084 Propionicacidemia 58 0.019
284
P DRM010 Dermatomyositis 58 0.019
285
CHL068 Cholestasis 58 0.019
286
TNS005 Tonsillitis 58 0.019
287
HMR004 Hemorrhagic Fever with Renal Syndrome 57 0.019
288
SNS001 Sensorineural Hearing Loss 57 0.019
289
ADR005 Adrenal Carcinoma 56 0.019
290
TRN015 Transient Cerebral Ischemia 56 0.019
291
P CHL002 Childhood Absence Epilepsy 56 0.019
292
PRP083 Porphyria, Acute Intermittent 55 0.019
293
c MYT020 Myotonic Dystrophy 2 55 0.019
294
P PRP019 Peripheral Nervous System Disease 54 0.019
295
PTN001 Patent Foramen Ovale 54 0.019
296
NWC001 Newcastle Disease 54 0.019
297
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 54 0.019
298
KRT002 Keratomalacia 54 0.019
299
P STC001 Stickler Syndrome 54 0.019
300
GTR002 Goiter 54 0.019
301
GST037 Gastroparesis 53 0.019
302
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.019
303
ALL026 Allergic Hypersensitivity Disease 53 0.019
304
P EMR001 Emery-Dreifuss Muscular Dystrophy 53 0.019
305
P LDD002 Liddle Syndrome 53 0.019
306
c ART115 Aortic Valve Disease 1 53 0.019
307
DRG003 Drug Dependence 53 0.019
308
P MYP101 Myopathy, Centronuclear 53 0.019
309
BNM001 Bone Marrow Cancer 52 0.019
310
LBR030 Leber Optic Atrophy 52 0.019
311
BRN071 Brain Injury 52 0.019
312
P END033 Endocarditis 52 0.019
313
TRY001 Trypanosomiasis 52 0.019
314
THY030 Thyroid Gland Disease 51 0.019
315
P PNM006 Pneumoconiosis 51 0.019
316
P DRR001 Diarrhea 51 0.019
317
c PRX045 Peroxisome Biogenesis Disorder 1b 51 0.019
318
c CNG464 Congenital Myopathy 50 0.019
319
c ACT071 Acute Kidney Failure 50 0.019
320
ERL001 Early Myoclonic Encephalopathy 50 0.019
321
INF034 Infective Endocarditis 50 0.019
322
c DYS166 Dysautonomia, Familial 50 0.019
323
IMP005 Impotence 50 0.019
324
HYP037 Hyperhomocysteinemia 50 0.019
325
SPR099 Supravalvar Aortic Stenosis 49 0.019
326
ADR012 Adrenal Gland Disease 49 0.019
327
PRT030 Parathyroid Gland Disease 49 0.019
328
P SMP007 Simpson-Golabi-Behmel Syndrome, Type 1 48 0.019
329
PLM041 Pulmonary Valve Stenosis 48 0.019
330
MTN003 Motion Sickness 48 0.019
331
MCR088 Microscopic Polyangiitis 48 0.019
332
CRN017 Coronary Thrombosis 48 0.019
333
P DYS021 Dysautonomia 47 0.019
334
NNN026 Noonan Syndrome with Multiple Lentigines 47 0.019
335
SXL003 Sexual Disorder 47 0.019
336
c HRT021 Heart Block, Progressive, Type Ia 47 0.019
337
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 47 0.019
338
SPC010 Speech and Communication Disorders 46 0.019
339
SNS023 Sensory System Cancer 46 0.019
340
DNN001 Danon Disease 45 0.019
341
ALN001 Aland Island Eye Disease 45 0.019
342
CLS010 Cluster Headache 45 0.019
343
VSC047 Vascular Malformation 45 0.019
344
RNL097 Renal Artery Disease 45 0.019
345
PHY002 Physical Disorder 44 0.019
346
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 44 0.019
347
CRD001 Cardiac Tamponade 44 0.019
348
DXT001 Dextrocardia 44 0.019
349
ATX003 Ataxia with Isolated Vitamin E Deficiency 44 0.019
350
AGR002 Agoraphobia 43 0.019
351
CRB008 Cerebral Atherosclerosis 43 0.019
352
SKN005 Skin Atrophy 43 0.019
353
STT002 Status Asthmaticus 43 0.019
354
ATN003 Autonomic Nervous System Neoplasm 43 0.019
355
FCT008 Factitious Disorder 43 0.019
356
GND003 Gonadal Disease 43 0.019
357
PRD011 Proud Syndrome 42 0.019
358
THL018 Thalassemia Major 42 0.019
359
P CRB088 Cerebral Atrophy 42 0.019
360
c LNG098 Long Qt Syndrome 14 42 0.019
361
ANT018 Anthracosis 42 0.019
362
HTR003 Heterotaxy 42 0.019
363
CPL007 Capillary Malformation-Arteriovenous Malformation 41 0.019
364
CRT008 Carotid Artery Dissection 41 0.019
365
P FML187 Familial Hypertension 41 0.019
366
ADR009 Adrenal Cortex Disease 41 0.019
367
PHC013 Phaeochromocytoma 41 0.019
368
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 41 0.019
369
HYP540 Hypertension, Diastolic 41 0.019
370
WTH001 Withdrawal Disorder 41 0.019
371
BRN080 Brain Ischemia 41 0.019
372
c CHR096 Chronic Pulmonary Heart Disease 40 0.019
373
MYF002 Myofascial Pain Syndrome 40 0.019
374
CHL028 Childhood Type Dermatomyositis 40 0.019
375
BLD054 Blood Protein Disease 40 0.019
376
THL017 Thalassemia Intermedia 40 0.019
377
c CNG031 Congenital Nervous System Abnormality 39 0.019
378
PLM068 Pulmonary Vein Stenosis 39 0.019
379
CPT003 Cpt Deficiency, Hepatic, Type Ia 39 0.019
380
CRN055 Carney Triad 39 0.019
381
NTR005 Nutritional Deficiency Disease 39 0.019
382
NSY001 N Syndrome 39 0.019
383
P HRT035 Heart Block, Congenital 39 0.019
384
MDY003 Mody, Type Ii 38 0.019
385
ADJ001 Adjustment Disorder 38 0.019
386
c MYP072 Myopathy, Myofibrillar, 1 38 0.019
387
ALC010 Alcoholic Cardiomyopathy 38 0.019
388
c LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 38 0.019
389
LNS003 Lens Disease 38 0.019
390
LYM029 Lymphedema-Distichiasis Syndrome 37 0.019
391
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.019
392
c ALP005 Alpha Chain Disease 37 0.019
393
TSH001 Tsh Producing Pituitary Tumor 36 0.019
394
PRP080 Peripheral Artery Disease 36 0.019
395
c MLG132 Malignant Hyperthermia Susceptibility 1 36 0.019
396
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 36 0.019
397
EPD019 Epidural Neoplasm 35 0.019
398
GLS004 Glossopharyngeal Neuralgia 35 0.019
399
P HYP599 Hypoparathyroidism, Familial Isolated 35 0.019
400
HTR014 Heterotaxy, Visceral, 1, X-Linked 35 0.019
401
c DNT021 Dent Disease 2 34 0.019
402
c CRD187 Cardiomyopathy, Dilated, 3b 34 0.019
403
DBT090 Diabetes and Deafness, Maternally Inherited 33 0.019
404
MDY006 Mody, Type Iv 33 0.019
405
KDN013 Kidney Hypertrophy 33 0.019
406
P ACT080 Acute Pulmonary Heart Disease 32 0.019
407
SCH068 Schwartz-Jampel Syndrome, Type 1 32 0.019
408
MGL023 Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome, Somatic 32 0.019
409
c CRD190 Cardiomyopathy, Hypertrophic, 2 32 0.019
410
c FML250 Familial Progressive Cardiac Conduction Defect 31 0.019
411
CRB031 Cerebral Arterial Disease 31 0.019
412
c AST037 Asthma 1 31 0.019
413
c AST039 Asthma 2 31 0.019
414
MTC028 Mitochondrial Cardiomyopathy 30 0.019
415
c STR089 Striatal Degeneration, Autosomal Dominant 2 30 0.019
416
THR099 Third-Degree Atrioventricular Block 30 0.019
417
EHL060 Ehlers-Danlos Syndrome Due to Tenascin X Deficiency 30 0.019
418
P ATR081 Atrial Standstill 30 0.019
419
NSP003 Nasopharyngeal Disease 30 0.019
420
c CNG404 Congenital Heart Defects, Multiple Types, 4 29 0.019
421
c PLM121 Pulmonary Hypertension, Primary, 4 29 0.019
422
P PTN008 Patent Arterial Duct 29 0.019
423
c CTS034 Cutis Laxa, Autosomal Recessive Type 1 29 0.019
424
c CRD198 Cardiomyopathy, Hypertrophic, 18 29 0.019
425
c VNT028 Ventricular Septal Defect 1 29 0.019
426
PST048 Postural Orthostatic Tachycardia Syndrome 28 0.019
427
c ATR038 Atrial Fibrillation, Familial, 3 28 0.019
428
PCW002 Pcwh Syndrome 28 0.019
429
c CRD107 Cardiomyopathy, Dilated, 1r 28 0.019
430
c SCL052 Scleroderma, Familial Progressive 27 0.019
431
ARR025 Arrhythmogenic Right Ventricular Dysplasia 5 27 0.019
432
CRD201 Cardiomyopathy, Dilated, 1c, with or Without Lvnc 27 0.019
433
EYC003 Eye Accommodation Disease 26 0.019
434
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 26 0.019
435
ARR038 Arrhythmogenic Right Ventricular Dysplasia 11 26 0.019
436
ANG060 Angiopathy, Hereditary, with Nephropathy, Aneurysms, and Muscle Cramps 26 0.019
437
c JRV002 Jervell and Lange-Nielsen Syndrome 2 26 0.019
438
SHP003 Shapiro Syndrome 25 0.019
439
c VNT024 Ventricular Septal Defect 3 25 0.019
440
c FML294 Familial Short Qt Syndrome 25 0.019
441
ARR035 Arrhythmogenic Right Ventricular Dysplasia 9 25 0.019
442
c GLY009 Glycogen Storage Disease Xv 25 0.019
443
ARR029 Arrhythmogenic Right Ventricular Dysplasia 8 24 0.019
444
c RNL016 Renal Infectious Disease 24 0.019
445
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 24 0.019
446
CRB087 Cerebral Arteriosclerosis 24 0.019
447
NTH002 Nathalie Syndrome 23 0.019
448
c CRD104 Cardiomyopathy, Dilated, 1p 23 0.019
449
RHM029 Rheumatic Fever-Related Antigen Rheumatic Fever, Acute, Susceptibility to, Included 23 0.019
450
c VNT026 Ventricular Septal Defect 2 23 0.019
451
NN2002 Non 24 Hour Sleep Wake Disorder 22 0.019
452
c SCK022 Sick Sinus Syndrome 3 22 0.019
453
SCN049 Second-Degree Atrioventricular Block 22 0.019
454
VSC009 Vascular Skin Disease 22 0.019
455
MCL055 Mcleod Syndrome with or Without Chronic Granulomatous Disease 22 0.019
456
APN006 Apnea of Prematurity 21 0.019
457
c RNL034 Renal Cell Carcinoma 4 21 0.019
458
c LFT017 Left Ventricular Noncompaction 8 21 0.019
459
c CRD173 Cardiomyopathy, Dilated, 1nn 21 0.019
460
ATN001 Autonomic Peripheral Neuropathy 20 0.019
461
c DLT014 Dilated Cardiomyopathy 1b 20 0.019
462
ARR041 Arrhythmogenic Right Ventricular Dysplasia, Familial, 13 20 0.019
463
c BRG010 Brugada Syndrome 8 20 0.019
464
HYP682 Hypertelorism, Teebi Type 19 0.019
465
c DBT058 Diabetes Mellitus, Insulin-Dependent, 7 19 0.019
466
CHR586 Chromosome 16p12.2-P11.2 Deletion Syndrome, 7.1- to 8.7-Mb 19 0.019
467
c BRG012 Brugada Syndrome 9 18 0.019
468
VNT009 Ventricular Tachycardia, Idiopathic 18 0.019
469
PLM008 Pulmonary Subvalvular Stenosis 18 0.019
470
c ATR025 Atrial Fibrillation, Familial, 2 17 0.019
471
HRT029 Heart Tumor of the Child 17 0.019
472
c HYP453 Hypertension, Essential 7 16 0.019
473
TBT001 Tabatznik Syndrome 16 0.019
474
HYD050 Hydrocephalus, Endocardial Fibroelastosis, and Cataracts 15 0.019
475
ARR036 Arrhythmogenic Right Ventricular Dysplasia 3 15 0.019
476
KNS006 Kniest-Like Dysplasia, Lethal 15 0.019
477
EPL095 Epilepsy with Myoclonic Absences 15 0.019
478
CRD023 Cardiomyopathy Cataract Hip Spine Disease 15 0.019
479
SBR011 Subaortic Stenosis--Short Stature Syndrome 14 0.019
480
WLL032 Woolly Hair, Hypotrichosis, Everted Lower Lip, and Outstanding Ears 14 0.019
481
ECT023 Ectodermal Dysplasia, Hidrotic, Christianson-Fourie Type 14 0.019
482
HRS003 Hirschsprung Disease Ganglioneuroblastoma 14 0.019
483
PNC065 Pinched Nerve 13 0.019
484
19P001 19p13.12 Microdeletion Syndrome 13 0.019
485
ARR005 Arrhythmogenic Right Ventricular Dysplasia/cardiomyopathy 2 13 0.019
486
THL008 Thalamic Degeneration, Symmetric Infantile 12 0.019
487
PLY127 Polyneuropathy-Intellectual Disability-Acromicria-Premature Menopause Syndrome 12 0.019
488
CNG288 Congenital Absence of Upper Arm and Forearm with Hand Present 11 0.019
489
ARR006 Arrhythmogenic Right Ventricular Dysplasia/cardiomyopathy 3 11 0.019
490
ART033 Aortic Valves Stenosis of the Child 11 0.019
491
MSC030 Muscular Fibrosis Multifocal Obstructed Vessels 10 0.019
492
TRS022 Torsade De Pointes, Short-Coupled Variant 6 0.019
493
P BRS047 Breast Cancer 100 0.013
494
P CLR023 Colorectal Cancer 97 0.013
495
P LNG032 Lung Cancer 94 0.013
496
P ALZ034 Alzheimer Disease 93 0.013
497
P OBS005 Obesity 93 0.013
498
HPT023 Hepatocellular Carcinoma 91 0.013
499
P PRS040 Prostate Cancer 89 0.013
500
P RHM011 Rheumatoid Arthritis 88 0.013
501
CYS001 Cystic Fibrosis 86 0.013
502
P PNC035 Pancreatic Cancer 85 0.013
503
HV1006 Hiv-1 82 0.013
504
P AST005 Asthma 82 0.013
505
P OST012 Osteoarthritis 82 0.013
506
P HNT016 Huntington Disease 80 0.013
507
MLR004 Malaria 79 0.013
508
GST053 Gastric Cancer 77 0.013
509
P HYP607 Hypercholesterolemia, Familial 77 0.013
510
P MDL005 Medulloblastoma 77 0.013
511
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 76 0.013
512
P SCH015 Schizophrenia 76 0.013
513
P OVR042 Ovarian Cancer 75 0.013
514
END057 Endometrial Cancer 75 0.013
515
P ART022 Arthritis 75 0.013
516
ESP021 Esophageal Cancer 75 0.013
517
P RTN024 Retinoblastoma 75 0.013
518
INS024 Insulin-Like Growth Factor I 74 0.013
519
c CHR090 Chronic Lymphocytic Leukemia 74 0.013
520
MYL009 Myelodysplastic Syndrome 74 0.013
521
TNG009 Tongue Squamous Cell Carcinoma 74 0.013
522
HDG012 Hodgkin Lymphoma 73 0.013
523
PHN003 Phenylketonuria 73 0.013
524
CMP005 Campomelic Dysplasia 72 0.013
525
c HPT073 Hepatitis C Virus 72 0.013
526
P LVR013 Liver Disease 72 0.013
527
P PRK057 Parkinson Disease, Late-Onset 72 0.013
528
P ALG002 Alagille Syndrome 72 0.013
529
WLS001 Wilson Disease 72 0.013
530
c LKM061 Leukemia, Acute Myeloid 71 0.013
531
c MCL042 Macular Degeneration, Age-Related, 1 71 0.013
532
MLT021 Multiple System Atrophy 71 0.013
533
MNT001 Mantle Cell Lymphoma 70 0.013
534
CRZ001 Crouzon Syndrome 70 0.013
535
SQM013 Squamous Cell Carcinoma, Head and Neck 70 0.013
536
P HPT021 Hepatitis 70 0.013
537
TST021 Testicular Germ Cell Tumor 70 0.013
538
BRN028 Brain Cancer 70 0.013
539
KRT004 Keratitis 70 0.013
540
P LKM002 Leukemia 70 0.013
541
P LYM118 Lymphoma 70 0.013
542
P ADN016 Adenocarcinoma 69 0.013
543
P NRB001 Neuroblastoma 69 0.013
544
TBR010 Tuberculosis 69 0.013
545
SCK003 Sickle Cell Anemia 68 0.013
546
ATT013 Attention Deficit-Hyperactivity Disorder 68 0.013
547
c MLT136 Multiple Endocrine Neoplasia 1 68 0.013
548
P PLM036 Pulmonary Fibrosis 68 0.013
549
c HPT001 Hepatitis C 68 0.013
550
SVR004 Severe Combined Immunodeficiency 68 0.013
551
P CWD006 Cowden Syndrome 1 68 0.013
552
THY028 Thyroid Cancer 68 0.013
553
P ESS003 Essential Thrombocythemia 68 0.013
554
PLM001 Pulmonary Tuberculosis 68 0.013
555
ART016 Aortic Aneurysm 67 0.013
556
P MYL005 Myelofibrosis 67 0.013
557
MLG108 Malignant Melanoma, Somatic 67 0.013
558
WRN001 Werner Syndrome 67 0.013
559
PSY004 Psychotic Disorder 67 0.013
560
c PNC108 Pancreatitis, Hereditary 67 0.013
561
BLD087 Bladder Cancer, Somatic 67 0.013
562
RNL101 Renal Cell Carcinoma, Papillary 67 0.013
563
P PNM007 Pneumonia 66 0.013
564
KPS004 Kaposi Sarcoma 66 0.013
565
P CHR071 Charcot-Marie-Tooth Disease 66 0.013
566
OBS002 Obsessive-Compulsive Disorder 66 0.013
567
SRC014 Sarcoma 66 0.013
568
OTT002 Otitis Media 66 0.013
569
P GLB002 Glioblastoma 66 0.013
570
CRV047 Cervical Cancer, Somatic 65 0.013
571
LYM115 Lymphoma, Non-Hodgkin 65 0.013
572
P AST007 Astrocytoma 65 0.013
573
ALC007 Alcohol Dependence 65 0.013
574
DWN001 Down Syndrome 65 0.013
575
P HYP117 Hypertriglyceridemia 65 0.013
576
DFC004 Deficiency Anemia 65 0.013
577
P HRP006 Herpes Simplex 65 0.013
578
BRC012 Brucellosis 65 0.013
579
P ORT004 Orthostatic Intolerance 65 0.013
580
P RBN001 Rubinstein-Taybi Syndrome 65 0.013
581
ART005 Arteriovenous Malformation 65 0.013
582
c BSL007 Basal Cell Carcinoma 64 0.013
583
P OST002 Osteoporosis 64 0.013
584
P PLR004 Pleuropulmonary Blastoma 64 0.013
585
P BCL006 B-Cell Lymphomas 64 0.013
586
c HPT016 Hepatitis B 64 0.013
587
ALL003 Allergic Rhinitis 64 0.013
588
DMN002 Dementia 64 0.013
589
PSR001 Psoriatic Arthritis 64 0.013
590
HMT002 Hematologic Cancer 64 0.013
591
P AGM001 Agammaglobulinemia 64 0.013
592
P ATS007 Autism Spectrum Disorder 64 0.013
593
P ALX003 Alexander Disease 64 0.013
594
EWN003 Ewing Sarcoma 64 0.013
595
PTR006 Peters Anomaly 64 0.013
596
CHR066 Chronic Fatigue Syndrome 64 0.013
597
P DYS154 Dystonia 64 0.013
598
P THR014 Thrombocytopenia 64 0.013
599
P PLZ001 Pelizaeus-Merzbacher Disease 64 0.013
600
MTH009 Mouth Disease 63 0.013
601
ATP002 Atopy 63 0.013
602
P ART023 Arthropathy 63 0.013
603
ACN011 Acne 63 0.013
604
P MCL013 Mucolipidosis Iv 63 0.013
605
BRN024 Bronchitis 63 0.013
606
OST085 Osteosarcoma, Somatic 63 0.013
607
PLY125 Polycythemia Vera, Somatic 63 0.013
608
EYD002 Eye Disease 63 0.013
609
P PSR002 Psoriasis 63 0.013
610
INC002 Inclusion Body Myositis 63 0.013
611
P SPN301 Spinocerebellar Ataxia 2 63 0.013
612
P LNG064 Lung Cancer Susceptibility 3 62 0.013
613
c KNN009 Kenny-Caffey Syndrome, Type 1 62 0.013
614
P ATP001 Atopic Dermatitis 62 0.013
615
P NRC002 Narcolepsy 62 0.013
616
APH001 Aphthous Stomatitis 62 0.013
617
PLM129 Pulmonary Disease, Chronic Obstructive 62 0.013
618
PRT036 Peritonitis 62 0.013
619
GLC037 Glucocorticoid Resistance 62 0.013
620
BRS051 Breast Disease 62 0.013
621
GLB015 Glioblastoma Multiforme 62 0.013
622
P ESP024 Esophagitis 62 0.013
623
P ADD001 Addison's Disease 62 0.013
624
VSC011 Vasculitis 62 0.013
625
INT146 Intervertebral Disc Disease 62 0.013
626
c ACT073 Acute Leukemia 62 0.013
627
OCL009 Ocular Cancer 62 0.013
628
SKN019 Skin Melanoma 62 0.013
629
P EHL001 Ehlers-Danlos Syndrome 61 0.013
630
GST092 Gastroesophageal Reflux 61 0.013
631
MDD011 Mood Disorder 61 0.013
632
TTN003 Tetanus 61 0.013
633
PRM097 Primary Immunodeficiency Disease 61 0.013
634
P ESN007 Eosinophilia 61 0.013
635
WST001 West Syndrome 61 0.013
636
DRM006 Dermatitis 61 0.013
637
TXC005 Toxic Shock Syndrome 61 0.013
638
P LYM025 Lymphedema 61 0.013
639
P PRS038 Personality Disorder 61 0.013
640
GLB001 Gilbert Syndrome 61 0.013
641
PLM134 Pulmonary Fibrosis, Idiopathic 61 0.013
642
c ESS001 Essential Tremor 61 0.013
643
P IDP010 Idiopathic Generalized Epilepsy 61 0.013
644
WLL001 Williams-Beuren Syndrome 61 0.013
645
P INT068 Intestinal Disease 61 0.013
646
TYP007 Typhoid Fever 61 0.013
647
c VRL010 Viral Hepatitis 61 0.013
648
VNW001 Von Willebrand's Disease 61 0.013
649
P INF032 Infertility 61 0.013
650
P RHN004 Rhinitis 61 0.013
651
P NPH009 Nephrolithiasis 60 0.013
652
P ASP006 Aspergillosis 60 0.013
653
ISB001 Isobutyryl-Coa Dehydrogenase Deficiency 60 0.013
654
P HML002 Hemolytic Anemia 60 0.013
655
P HMN010 Hemangioma 60 0.013
656
GNG013 Gingivitis 60 0.013
657
P TMP003 Temporal Arteritis 60 0.013
658
P PNC044 Pancreatitis 60 0.013
659
P LYM026 Lymphoblastic Leukemia 60 0.013
660
P ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 60 0.013
661
P ADL010 Adult Respiratory Distress Syndrome 60 0.013
662
P GST049 Gastrointestinal System Cancer 60 0.013
663
HYP066 Hyperglycemia 60 0.013
664
c MNN043 Meningioma, Familial 60 0.013
665
c MCL062 Mucolipidosis Ii Alpha/beta 60 0.013
666
P SPN052 Spondyloarthropathy 60 0.013
667
c EHL057 Ehlers-Danlos Syndrome, Type Iv 60 0.013
668
P SNS014 Sinusitis 60 0.013
669
c MCR115 Microvascular Complications of Diabetes 5 60 0.013
670
FTT001 Fatty Liver Disease 60 0.013
671
P HYP055 Hypoplastic Left Heart Syndrome 60 0.013
672
ETN001 Eating Disorder 60 0.013
673
c ATM010 Autoimmune Hemolytic Anemia 60 0.013
674
P SHR029 Short Syndrome 60 0.013
675
P CRN139 Cornelia De Lange Syndrome 1 60 0.013
676
c EXD008 Exudative Vitreoretinopathy 1 60 0.013
677
P PNC025 Panic Disorder 60 0.013
678
GST045 Gastroenteritis 60 0.013
679
P ALC004 Alcohol Abuse 60 0.013
680
P BRS044 Breast Adenocarcinoma 60 0.013
681
KRN002 Kearns-Sayre Syndrome 59 0.013
682
P LRY044 Larynx Cancer 59 0.013
683
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.013
684
P MYP006 Myopia 59 0.013
685
P CTS001 Cutis Laxa 59 0.013
686
P PRT013 Portal Hypertension 59 0.013
687
P UVT001 Uveitis 59 0.013
688
P CMR001 Camurati-Engelmann Disease 59 0.013
689
ETH011 Ethylmalonic Encephalopathy 59 0.013
690
CRV038 Cervical Squamous Cell Carcinoma 59 0.013
691
VRL011 Viral Infectious Disease 59 0.013
692
MSS002 Mass Syndrome 59 0.013
693
c CNG006 Congenital Hypothyroidism 59 0.013
694
CHY002 Chylomicron Retention Disease 59 0.013
695
ALC006 Alcoholic Hepatitis 59 0.013
696
ATS001 Autistic Disorder 59 0.013
697
MTR014 Motor Neuron Disease 59 0.013
698
CLT003 Colitis 59 0.013
699
c HPT003 Hepatitis a 59 0.013
700
P THR015 Thrombophilia 59 0.013
701
P FCL005 Focal Segmental Glomerulosclerosis 59 0.013
702
P HYP060 Hyperinsulinism 59 0.013
703
P GLL020 Gallbladder Disease 59 0.013
704
PRP030 Purpura 59 0.013
705
URT039 Urticaria 59 0.013
706
P GLY013 Glycogen Storage Disease 59 0.013
707
DBT087 Diabetes Insipidus, Neurohypophyseal 59 0.013
708
MRB003 Morbid Obesity 58 0.013
709
MLN054 Melanocytic Nevus Syndrome, Congenital, Somatic 58 0.013
710
CMM005 Common Cold 58 0.013
711
LPD008 Lipid Metabolism Disorder 58 0.013
712
c SRC025 Sarcoidosis 1 58 0.013
713
INT066 Interstitial Lung Disease 58 0.013
714
P MCR010 Microcephaly 58 0.013
715
DPH001 Diphtheria 58 0.013
716
ALL006 Allergic Asthma 58 0.013
717
P HLT001 Holt-Oram Syndrome 58 0.013
718
c GLY060 Glycogen Storage Disease Ia 58 0.013
719
RHB003 Rhabdomyosarcoma 58 0.013
720
P ORL007 Oral Cavity Cancer 58 0.013
721
FLL027 Fallopian Tube Carcinoma 58 0.013
722
P GLM045 Glioma 58 0.013
723
c ADL017 Adult T-Cell Leukemia 58 0.013
724
PHR003 Pharyngitis 58 0.013
725
CRT002 Cartilage-Hair Hypoplasia 58 0.013
726
LPM004 Lipoma 58 0.013
727
P CTR002 Cataract 57 0.013
728
RTN017 Retinal Detachment 57 0.013
729
P PRC031 Preeclampsia/eclampsia 1 57 0.013
730
RHM027 Rheumatic Disease 57 0.013
731
PNC034 Pancreas Disease 57 0.013
732
PST028 Post-Traumatic Stress Disorder 57 0.013
733
P HYP069 Hyperparathyroidism 57 0.013
734
MCR264 Mcardle Disease 57 0.013
735
P MTR004 Maturity-Onset Diabetes of the Young 57 0.013
736
P FRS003 Fraser Syndrome 57 0.013
737
EXF001 Exfoliation Syndrome 57 0.013
738
MLG056 Malignant Hyperthermia 57 0.013
739
PRR007 Perry Syndrome 57 0.013
740
CTS003 Coats Disease 57 0.013
741
ING001 Inguinal Hernia 57 0.013
742
P HMR003 Hemorrhagic Disease 57 0.013
743
P INT001 Intrahepatic Cholestasis 57 0.013
744
PLY023 Polycystic Liver Disease 57 0.013
745
c THR082 Thrombophilia Due to Activated Protein C Resistance 57 0.013
746
ABL002 Ablepharon-Macrostomia Syndrome 57 0.013
747
YLL002 Yellow Fever 57 0.013
748
P MCR129 Microvascular Complications of Diabetes 1 57 0.013
749
P THR003 Thoracic Aortic Aneurysm 57 0.013
750
P PLY018 Polycythemia 57 0.013
751
c FML108 Familial Breast Cancer 57 0.013
752
P INT143 Interstitial Cystitis 57 0.013
753
ERY003 Erythema Multiforme 57 0.013
754
P HYP040 Hypospadias 57 0.013
755
c ACT210 Acute Respiratory Distress Syndrome 57 0.013
756
CNS004 Constipation 57 0.013
757
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 57 0.013
758
IDP011 Idiopathic Interstitial Pneumonia 57 0.013
759
P BRN009 Burning Mouth Syndrome 57 0.013
760
P SML001 Small Cell Carcinoma 57 0.013
761
EMB004 Embryonal Carcinoma 56 0.013
762
TRG002 Trigeminal Neuralgia 56 0.013
763
P GLM007 Glomerulonephritis 56 0.013
764
STR026 Star Syndrome 56 0.013
765
DFF005 Diffuse Large B-Cell Lymphoma 56 0.013
766
CHL067 Cholecystitis 56 0.013
767
SBS003 Substance Abuse 56 0.013
768
P SCL018 Scoliosis 56 0.013
769
HPT019 Hepatic Encephalopathy 56 0.013
770
ORL015 Oral Squamous Cell Carcinoma 56 0.013
771
P INT070 Intestinal Obstruction 56 0.013
772
EMP007 Emphysema Due to Aat Deficiency 56 0.013
773
NRP015 Neuropathy, Congenital Hypomyelinating 56 0.013
774
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 56 0.013
775
SFT003 Soft Tissue Sarcoma 56 0.013
776
JNT002 Joint Disorders 56 0.013
777
RTN018 Retinal Disease 56 0.013
778
c THR092 Thrombophilia Due to Thrombin Defect 56 0.013
779
P PTS002 Ptosis 56 0.013
780
BRN002 Bronchiolitis 56 0.013
781
HRP004 Herpes Zoster 56 0.013
782
PLM010 Pulmonary Edema 56 0.013
783
c ACT027 Acute Pancreatitis 56 0.013
784
INT002 Intermittent Claudication 56 0.013
785
URN010 Urinary Tract Obstruction 56 0.013
786
PRS047 Prostatitis 56 0.013
787
P MMB011 Membranous Nephropathy 56 0.013
788
MLN007 Male Infertility 56 0.013
789
SPN027 Spinal Stenosis 56 0.013
790
MSC077 Muscle Eye Brain Disease 56 0.013
791
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 55 0.013
792
ORL011 Oral Cancer 55 0.013
793
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.013
794
CRT016 Carotid Artery Disease 55 0.013
795
P OVR049 Ovarian Disease 55 0.013
796
DBT010 Diabetic Neuropathy 55 0.013
797
CHN016 Cohen Syndrome 55 0.013
798
DMY004 Demyelinating Disease 55 0.013
799
c PRK031 Parkinson Disease 1 55 0.013
800
P PLY017 Polyarteritis Nodosa 55 0.013
801
GST023 Gastric Ulcer 55 0.013
802
THR004 Thrombocytosis 55 0.013
803
GLC003 Glucose Intolerance 55 0.013
804
HDN004 Head and Neck Carcinoma 55 0.013
805
PNC033 Pancreas Adenocarcinoma 55 0.013
806
P MLT074 Multiple Endocrine Neoplasia 55 0.013
807
DSS008 Disease of Mental Health 55 0.013
808
CPR001 Coproporphyria 55 0.013
809
RCT018 Rectal Neoplasm 55 0.013
810
P OLG002 Oligodendroglioma 55 0.013
811
CRB037 Cerebral Palsy 54 0.013
812
MVM001 Movement Disease 54 0.013
813
GST050 Gastrointestinal System Disease 54 0.013
814
BRN038 Bronchial Disease 54 0.013
815
VSC002 Vascular Dementia 54 0.013
816
P ECL001 Eclampsia 54 0.013
817
PLS007 Plasmodium Falciparum Malaria 54 0.013
818
CLR003 Clear Cell Adenocarcinoma 54 0.013
819
c OPT055 Optic Atrophy Plus Syndrome 54 0.013
820
NRN004 Neuroendocrine Tumor 54 0.013
821
PLM034 Pulmonary Emphysema 54 0.013
822
P TRM003 Tremor 54 0.013
823
P HYP345 Hyper-Ige Recurrent Infection Syndrome 54 0.013
824
HDC001 Headache 54 0.013
825
RST001 Restless Legs Syndrome 54 0.013
826
c ALZ037 Alzheimer Disease-2 54 0.013
827
P EXP004 Exophthalmos 54 0.013
828
VSC006 Vascular Cancer 54 0.013
829
P SML016 Small Intestine Cancer 54 0.013
830
P INT030 Intracranial Aneurysm 54 0.013
831
MCN017 Meconium Ileus 54 0.013
832
KLP010 Klippel-Trenaunay-Weber Syndrome 54 0.013
833
HMP005 Hemiplegia 54 0.013
834
c PRM126 Primary Peritoneal Carcinoma 54 0.013
835
VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 54 0.013
836
PLM012 Pulmonary Sarcoidosis 54 0.013
837
c HPT007 Hepatitis E 54 0.013
838
FDL002 Food Allergy 54 0.013
839
P RTN016 Retinal Degeneration 54 0.013
840
BLM002 Bulimia Nervosa 54 0.013
841
P VNS003 Venous Insufficiency 53 0.013
842
P END044 Endometriosis 53 0.013
843
PST046 Post-Transplant Lymphoproliferative Disease 53 0.013
844
P LPC002 Lip Cancer 53 0.013
845
ACT008 Actinic Keratosis 53 0.013
846
HMR039 Hemorrhage, Intracerebral 53 0.013
847
P INT063 Intellectual Disability 53 0.013
848
RSC001 Rosacea 53 0.013
849
P STR020 Strabismus 53 0.013
850
ART002 Arts Syndrome 53 0.013
851
C3D001 C3 Deficiency 53 0.013
852
GLM004 Gliomatosis Cerebri 53 0.013
853
PYR010 Peyronie's Disease 53 0.013
854
SML033 Small Cell Cancer of the Lung, Somatic 53 0.013
855
GST027 Gastric Lymphoma 53 0.013
856
SMT006 Somatoform Disorder 53 0.013
857
LYM019 Lymphosarcoma 53 0.013
858
DGN001 Degenerative Disc Disease 53 0.013
859
ESP023 Esophageal Disease 53 0.013
860
PLV003 Pelvic Inflammatory Disease 53 0.013
861
P SYP003 Syphilis 53 0.013
862
P DBT005 Diabetes Insipidus 53 0.013
863
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 53 0.013
864
P LYM033 Lymphoproliferative Syndrome 53 0.013
865
PLS006 Plasmodium Vivax Malaria 53 0.013
866
INT075 Intracranial Hypertension 53 0.013
867
NNL002 Nonalcoholic Steatohepatitis 53 0.013
868
P SJG001 Sjogren's Syndrome 53 0.013
869
RDC002 Radiculopathy 53 0.013
870
P CNT005 Central Nervous System Lymphoma 53 0.013
871
P ANG015 Angioedema 53 0.013
872
P CYS018 Cystitis 53 0.013
873
CRV040 Cervix Carcinoma 53 0.013
874
c INS002 in Situ Carcinoma 52 0.013
875
END035 Endocrine Gland Cancer 52 0.013
876
LYS002 Lysosomal Storage Disease 52 0.013
877
P LPD010 Lipodystrophy 52 0.013
878
TRM010 Traumatic Brain Injury 52 0.013
879
c HPT015 Hepatitis D 52 0.013
880
TTH006 Tooth Disease 52 0.013
881
c LKM060 Leukemia, Acute Lymphoblastic 3 52 0.013
882
TLN003 Telangiectasis 52 0.013
883
THR016 Thrombophlebitis 52 0.013
884
PRT014 Protein S Deficiency 52 0.013
885
CRH005 Crohn's Colitis 52 0.013
886
PRS042 Prostate Disease 52 0.013
887
DBT062 Diabetic Foot Ulcers 52 0.013
888
ANG020 Angiosarcoma 52 0.013
889
c PRK059 Parkinson Disease 8 52 0.013
890
BLT006 Bilateral Breast Cancer 52 0.013
891
RSS002 Roussy-Levy Syndrome 52 0.013
892
P ART061 Arthrogryposis, Distal, Type 2a 52 0.013
893
PNM008 Pneumothorax 52 0.013
894
MST017 Mast Cell Disease 52 0.013
895
P MTC069 Mitochondrial Disorders 52 0.013
896
P LTR001 Lateral Sclerosis 52 0.013
897
NCT008 Nicotine Dependence, Protection Against 52 0.013
898
GST040 Gastric Adenocarcinoma 52 0.013
899
CHC001 Chickenpox 52 0.013
900
P CPL006 Capillary Hemangioma 52 0.013
901
PLR022 Pleural Disease 52 0.013
902
P ERY008 Erythromelalgia 52 0.013
903
SRS001 Serous Cystadenocarcinoma 52 0.013
904
NRF007 Neurofibroma 52 0.013
905
BRS099 Breast Ductal Carcinoma 52 0.013
906
FRB001 Farber Lipogranulomatosis 51 0.013
907
MYM001 Myoma 51 0.013
908
PRT058 Pure Autonomic Failure 51 0.013
909
BLR001 Biliary Atresia 51 0.013
910
TXC002 Toxic Encephalopathy 51 0.013
911
DRY001 Dry Eye Syndrome 51 0.013
912
TMP001 Temporal Lobe Epilepsy 51 0.013
913
GNR004 Generalized Anxiety Disorder 51 0.013
914
c RTN162 Retinitis Pigmentosa 2 51 0.013
915
DBT004 Diabetic Polyneuropathy 51 0.013
916
PHL006 Phelan-Mcdermid Syndrome 51 0.013
917
CRC006 Carcinoid Syndrome 51 0.013
918
c DYS169 Dystonia-12 51 0.013
919
PRT011 Protein C Deficiency 51 0.013
920
GNG011 Gingival Disease 51 0.013
921
DSS009 Disseminated Intravascular Coagulation 51 0.013
922
c ALZ036 Alzheimer Disease, Type 3 51 0.013
923
ANG054 Angina Pectoris 51 0.013
924
BRX001 Bruxism 51 0.013
925
MSC072 Muscle Cancer 51 0.013
926
P HYP071 Hypersensitivity Reaction Type Ii Disease 51 0.013
927
P HYP065 Hyperaldosteronism 51 0.013
928
P MGR003 Migraine with Aura 51 0.013
929
CYT008 Cytomegalovirus Infection 51 0.013
930
RTN015 Retinal Cancer 51 0.013
931
c INF067 Inflammatory Bowel Disease 10 51 0.013
932
MYC002 Mycobacterium Avium Complex Disease 51 0.013
933
P KRT007 Keratoconus 51 0.013
934
DRG011 Drug Addiction 51 0.013
935
BRN004 Brain Edema 51 0.013
936
c PRM012 Primary Polycythemia 51 0.013
937
c INF071 Inflammatory Bowel Disease 1 51 0.013
938
OPT006 Optic Nerve Disease 51 0.013
939
FML038 Female Reproductive Organ Cancer 51 0.013
940
BLR006 Biliary Tract Disease 51 0.013
941
ADT003 Auditory System Disease 51 0.013
942
P DWL002 Dowling-Degos Disease 1 51 0.013
943
BLD044 Bladder Disease 51 0.013
944
KLD001 Keloids 51 0.013
945
PTH002 Pathological Gambling 51 0.013
946
FML037 Female Breast Cancer 51 0.013
947
P OCL002 Oculocutaneous Albinism 51 0.013
948
c LYM110 Lymphedema, Hereditary, Ia 51 0.013
949
RHM028 Rheumatic Heart Disease 51 0.013
950
P FML035 Familial Hyperlipidemia 50 0.013
951
CLR109 Colorectal Adenocarcinoma 50 0.013
952
P HRD018 Hair Disease 50 0.013
953
CLN019 Colonic Disease 50 0.013
954
MRC001 Marchiafava Bignami Disease 50 0.013
955
PNN001 Panniculitis 50 0.013
956
c FML053 Familial Colorectal Cancer 50 0.013
957
SPN051 Spondylitis 50 0.013
958
c INF023 Inflammatory Breast Carcinoma 50 0.013
959
SBS004 Substance Dependence 50 0.013
960
P CTN015 Cutaneous T Cell Lymphoma 50 0.013
961
MCN001 Mucinous Adenocarcinoma 50 0.013
962
STM006 Stomach Disease 50 0.013
963
LYM024 Lymphatic System Disease 50 0.013
964
IMM136 Immune System Disease 50 0.013
965
c ACT068 Acute Cystitis 50 0.013
966
INN002 Inner Ear Disease 50 0.013
967
OST016 Osteochondrosis 50 0.013
968
HMG005 Hemoglobinopathy 50 0.013
969
IGG001 Iga Glomerulonephritis 50 0.013
970
SCT005 Scott Syndrome 50 0.013
971
DYS014 Dyspepsia 50 0.013
972
FCL012 Facial Paralysis 50 0.013
973
P HYP014 Hyperuricemia 50 0.013
974
c GLY019 Glycogen Storage Disease Iiia 50 0.013
975
OPT003 Opiate Dependence 50 0.013
976
CDS001 Cadasil 50 0.013
977
RTN020 Retinal Vascular Disease 50 0.013
978
P RST002 Restrictive Cardiomyopathy 50 0.013
979
c ACT134 Acute Liver Failure 50 0.013
980
INT253 Intestinal Benign Neoplasm 50 0.013
981
P LMB006 Limb-Girdle Muscular Dystrophy 50 0.013
982
KRT009 Keratosis 50 0.013
983
RHM001 Rheumatic Fever 50 0.013
984
PST095 Post-Thrombotic Syndrome 50 0.013
985
STR081 Stormorken Syndrome 50 0.013
986
BCL002 B Cell Deficiency 50 0.013
987
STM007 Stomatitis 50 0.013
988
PRV006 Pervasive Developmental Disorder 50 0.013
989
MGR028 Migraine with or Without Aura 1 50 0.013
990
OVR063 Overnutrition 49 0.013
991
MSC006 Muscle Glycogenosis 49 0.013
992
NDL013 Nodular Regenerative Hyperplasia 49 0.013
993
CNN003 Conn's Syndrome 49 0.013
994
CLN015 Colon Adenocarcinoma 49 0.013
995
LPD009 Lipid Storage Disease 49 0.013
996
P CLL015 Collagen Disease 49 0.013
997
TCD001 Tic Disorder 49 0.013
998
P NGH001 Night Blindness 49 0.013
999
SRT004 Serotonin Syndrome 49 0.013
1000
PST021 Postpartum Depression 49 0.013
1001
HMN014 Human Immunodeficiency Virus Infectious Disease 49 0.013
1002
ESN005 Eosinophilic Gastroenteritis 49 0.013
1003
RLP001 Relapsing Polychondritis 49 0.013
1004
CNT007 Central Nervous System Tuberculosis 49 0.013
1005
MSS001 Masa Syndrome 49 0.013
1006
BRD001 Brody Myopathy 49 0.013
1007
PRM028 Paramyotonia Congenita 49 0.013
1008
CLC006 Calcinosis 49 0.013
1009
P PNV001 Panuveitis 49 0.013
1010
DYS073 Dysphagia 49 0.013
1011
MLL012 Miller Syndrome 49 0.013
1012
THR013 Thoracic Outlet Syndrome 49 0.013
1013
c PRM226 Primary Central Nervous System Lymphoma 49 0.013
1014
SLV003 Salivary Gland Disease 49 0.013
1015
P CHR345 Chronic Pain 49 0.013
1016
c ANT034 Anterior Uveitis 49 0.013
1017
CLL003 Cellulitis 49 0.013
1018
c INH020 Inherited Metabolic Disorder 49 0.013
1019
CHR056 Chronic Tic Disorder 49 0.013
1020
PRT018 Portal Vein Thrombosis 49 0.013
1021
SCK005 Sickle Cell Disease 49 0.013
1022
c CHR418 Chronic Leukemia 48 0.013
1023
ICH054 Ichthyosis, X-Linked 48 0.013
1024
RTC005 Reticulosarcoma 48 0.013
1025
HND002 Hand, Foot and Mouth Disease 48 0.013
1026
GRW007 Growth Hormone Deficiency 48 0.013
1027
LBL001 Lobular Neoplasia 48 0.013
1028
MTB004 Metabolic Acidosis 48 0.013
1029
URT004 Urethral Syndrome 48 0.013
1030
ALC009 Alcoholic Liver Cirrhosis 48 0.013
1031
BRN032 Brain Glioma 48 0.013
1032
FML039 Female Reproductive System Disease 48 0.013
1033
NRM004 Neuroma 48 0.013
1034
c CNG027 Congenital Hemolytic Anemia 48 0.013
1035
c CLL013 Cell Type Cancer 48 0.013
1036
PRV004 Periventricular Leukomalacia 48 0.013
1037
c SVR005 Severe Pre-Eclampsia 48 0.013
1038
RTN003 Retinal Ischemia 48 0.013
1039
ACT017 Acute Chest Syndrome 48 0.013
1040
SPN041 Spinal Cord Disease 48 0.013
1041
c HRM005 Hermansky-Pudlak Syndrome 1 48 0.013
1042
DPM001 Dopamine Beta-Hydroxylase Deficiency 48 0.013
1043
P OPN001 Open-Angle Glaucoma 48 0.013
1044
GLT021 Glutaricaciduria, Type I 48 0.013
1045
HYP141 Hyperphenylalaninemia 48 0.013