Search results for arrhythmia

1558 hits were found for arrhythmia

# Family MCID Name MIFTS Score
1
CRD054 Cardiac Arrhythmia, Ankyrin-B-Related 24 4.698
2
LNG104 Language Delay and Attention Deficit-Hyperactivity Disorder/cognitive Impairment with or Without Cardiac Arrhythmia 15 3.838
3
CRD223 Cardiac Arrhythmia 52 3.780
4
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 39 3.332
5
c CRD099 Cardiomyopathy, Dilated, 1e 53 3.310
6
INT313 Intellectual Developmental Disorder with Cardiac Arrhythmia 16 2.756
7
PHC009 Phocomelia Ectrodactyly Deafness Sinus Arrhythmia 14 2.751
8
RCR029 Recurrent Metabolic Encephalomyopathic Crises-Rhabdomyolysis-Cardiac Arrhythmia-Intellectual Disability Syndrome 7 2.745
9
PHC016 Phocomelia-Ectrodactyly, Ear Malformation, Deafness, and Sinus Arrhythmia 19 2.739
10
TNG012 Tango2-Related Metabolic Encephalopathy and Arrhythmias 3 2.709
11
WLF001 Wolff-Parkinson-White Syndrome 57 1.989
12
SDD004 Sudden Arrhythmia Death Syndrome 10 1.960
13
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 35 1.945
14
OGD001 Ogden Syndrome 35 1.945
15
c MSC140 Muscular Dystrophy, Limb-Girdle, Type 2x 22 1.945
16
SNT004 Sinoatrial Node Dysfunction and Deafness 16 1.901
17
P HRT032 Heart Disease 80 0.190
18
P ATR011 Atrial Fibrillation 68 0.163
19
P MYC007 Myocardial Infarction 81 0.142
20
P LNG028 Long Qt Syndrome 63 0.126
21
P CRD132 Cardiac Conduction Defect 53 0.119
22
CRD119 Cardiac Arrest 63 0.111
23
ISC004 Ischemia 66 0.106
24
P BRG001 Brugada Syndrome 61 0.102
25
SYN036 Syncope 46 0.100
26
P DLT002 Dilated Cardiomyopathy 76 0.098
27
CNG034 Congestive Heart Failure 74 0.097
28
P CRN018 Coronary Artery Anomaly 69 0.097
29
c ACT075 Acute Myocardial Infarction 64 0.095
30
ISC006 Ischemic Heart Disease 73 0.091
31
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 61 0.091
32
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 54 0.091
33
P CRN300 Coronary Heart Disease 1 57 0.090
34
P PRX010 Paroxysmal Ventricular Fibrillation 28 0.080
35
P HYP061 Hypertrophic Cardiomyopathy 65 0.078
36
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 59 0.078
37
P SCK002 Sick Sinus Syndrome 53 0.078
38
P ORT004 Orthostatic Intolerance 68 0.076
39
HYP005 Hypokalemia 53 0.074
40
P MSC005 Muscular Dystrophy 66 0.072
41
ART140 Arteries, Anomalies of 51 0.072
42
P MYT002 Myotonic Dystrophy 50 0.072
43
CRD003 Cardiac Sarcoidosis 40 0.072
44
P MYC008 Myocarditis 58 0.069
45
FNT004 Fainting 36 0.067
46
AGN016 Aging 65 0.062
47
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 57 0.062
48
P ART021 Arteriosclerosis 62 0.060
49
ANR040 Aneurysm 61 0.060
50
VSC007 Vascular Disease 71 0.057
51
P TTR001 Tetralogy of Fallot 70 0.057
52
c MYT021 Myotonic Dystrophy 1 68 0.057
53
P SLP006 Sleep Apnea 65 0.057
54
c ATR087 Atrial Standstill 1 59 0.057
55
P EPL164 Epilepsy 70 0.054
56
P MYP004 Myopathy 69 0.054
57
P NRP001 Neuropathy 63 0.054
58
HYP056 Hypoglycemia 62 0.054
59
c BLD140 Blood Group, I System 37 0.054
60
ATR057 Atrioventricular Block 52 0.051
61
TRN044 Transposition of the Great Arteries 49 0.051
62
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 33 0.051
63
P NRV007 Nervous System Disease 75 0.047
64
CHG001 Chagas Disease 72 0.047
65
P KDN018 Kidney Disease 69 0.047
66
c LNG044 Long Qt Syndrome 1 61 0.047
67
P ENC018 Encephalopathy 58 0.047
68
BRN106 Burns 57 0.047
69
HYP006 Hypertensive Heart Disease 51 0.047
70
SYS003 Systolic Heart Failure 44 0.047
71
ATR055 Atrial Septal Aneurysm 27 0.047
72
P DBT009 Diabetes Mellitus 72 0.044
73
c CHR089 Chronic Kidney Failure 72 0.044
74
c CNT035 Central Nervous System Disease 65 0.044
75
THR024 Thrombosis 61 0.044
76
HYP266 Hypoxia 61 0.044
77
P HYP370 Hypokalemic Periodic Paralysis, Type 1 59 0.044
78
SLP005 Sleep Disorder 59 0.044
79
END030 End Stage Renal Failure 59 0.044
80
P PLY041 Polymyositis 57 0.044
81
c PRG042 Progressive Familial Heart Block, Type Ia 57 0.044
82
P HYP076 Hyperthyroidism 56 0.044
83
SPS003 Spastic Diplegia 55 0.044
84
P JRV004 Jervell and Lange-Nielsen Syndrome 1 54 0.044
85
P LFT003 Left Ventricular Noncompaction 52 0.044
86
TMT001 Timothy Syndrome 52 0.044
87
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 47 0.044
88
ATN004 Autonomic Neuropathy 46 0.044
89
HRT012 Heart Valve Disease 45 0.044
90
CRD137 Cardiogenic Shock 45 0.044
91
HYP017 Hypophosphatemia 45 0.044
92
CRN041 Carnitine-Acylcarnitine Translocase Deficiency 44 0.044
93
c SHR030 Short Qt Syndrome 42 0.044
94
CRN302 Carnitine Palmitoyltransferase Ii Deficiency, Lethal Neonatal 28 0.044
95
P RTT002 Rett Syndrome 82 0.040
96
MSC157 Muscular Dystrophy, Duchenne Type 74 0.040
97
FBR012 Fabry Disease 72 0.040
98
P RSP003 Respiratory Failure 71 0.040
99
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.040
100
SDD001 Sudden Infant Death Syndrome 61 0.040
101
c CRD093 Cardiomyopathy, Dilated, 1a 58 0.040
102
URN009 Urinary System Disease 58 0.040
103
CRN296 Carnitine Palmitoyltransferase Ii Deficiency, Infantile 55 0.040
104
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 55 0.040
105
P SZR006 Seizure Disorder 55 0.040
106
P THY054 Thyrotoxic Periodic Paralysis 54 0.040
107
MSC033 Muscle Disorders 53 0.040
108
BRT005 Barth Syndrome 52 0.040
109
P PRC012 Pericardial Effusion 52 0.040
110
ATN005 Autonomic Dysfunction 51 0.040
111
DNN001 Danon Disease 47 0.040
112
RGH001 Right Bundle Branch Block 44 0.040
113
DBT002 Diabetic Autonomic Neuropathy 43 0.040
114
CRB009 Cerebritis 41 0.040
115
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.040
116
GLC008 Glucose Metabolism Disease 38 0.040
117
c LPD035 Lipodystrophy, Congenital Generalized, Type 4 36 0.040
118
c LNG056 Long Qt Syndrome 12 36 0.040
119
c BRG005 Brugada Syndrome 1 35 0.040
120
c HMC039 Hemochromatosis, Type 1 71 0.036
121
P MNN013 Meningitis 71 0.036
122
c BTT014 Beta-Thalassemia 70 0.036
123
ACR007 Acromegaly 70 0.036
124
P ATS364 Autism 70 0.036
125
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 70 0.036
126
P AMY004 Amyloidosis 69 0.036
127
P ANR048 Aniridia 1 68 0.036
128
CRB039 Cerebrovascular Disease 68 0.036
129
P SYS005 Systemic Scleroderma 67 0.036
130
LNG099 Lung Disease 67 0.036
131
APN008 Apnea, Obstructive Sleep 67 0.036
132
CST001 Costello Syndrome 67 0.036
133
SPN186 Spinal Cord Injury 67 0.036
134
c ART101 Aortic Valve Disease 2 65 0.036
135
RSP006 Respiratory System Disease 63 0.036
136
RFS006 Refsum Disease, Classic 63 0.036
137
NRM005 Neuromuscular Disease 60 0.036
138
P DRR001 Diarrhea 60 0.036
139
P PLY019 Polyneuropathy 58 0.036
140
P OCL013 Oculodentodigital Dysplasia 57 0.036
141
HYP052 Hyperkalemic Periodic Paralysis 57 0.036
142
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.036
143
PRP009 Peripartum Cardiomyopathy 53 0.036
144
CRN030 Coronary Stenosis 52 0.036
145
c CRD233 Cardiomyopathy, Dilated, 1b 51 0.036
146
c LNG047 Long Qt Syndrome 2 49 0.036
147
c ACT076 Acute Myocarditis 48 0.036
148
P DYS021 Dysautonomia 47 0.036
149
FDB001 Foodborne Botulism 46 0.036
150
c LNG048 Long Qt Syndrome 3 46 0.036
151
STT002 Status Asthmaticus 46 0.036
152
CRD001 Cardiac Tamponade 45 0.036
153
P MYF003 Myofibrillar Myopathy 44 0.036
154
c LNG050 Long Qt Syndrome 5 43 0.036
155
c FML191 Familial Long Qt Syndrome 43 0.036
156
TSH001 Tsh Producing Pituitary Tumor 42 0.036
157
c LNG051 Long Qt Syndrome 6 42 0.036
158
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.036
159
c PRG043 Progressive Familial Heart Block, Type Ib 40 0.036
160
c LNG053 Long Qt Syndrome 9 40 0.036
161
MSC004 Muscle Tissue Disease 39 0.036
162
c LNG057 Long Qt Syndrome 13 39 0.036
163
GNT019 Giant Cell Myocarditis 34 0.036
164
HMP001 Hemopericardium 34 0.036
165
c FML294 Familial Short Qt Syndrome 34 0.036
166
CRD231 Cardiomyopathy, Infantile Histiocytoid 27 0.036
167
c GLY009 Glycogen Storage Disease Xv 26 0.036
168
c EMR020 Emery-Dreifuss Muscular Dystrophy 3, Autosomal Recessive 25 0.036
169
ANR038 Anorexia Nervosa 1 21 0.036
170
ATS285 Autosomal Semi-Dominant Severe Lipodystrophic Laminopathy 17 0.036
171
BLD137 Blood Group--Ahonen 17 0.036
172
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.031
173
c HYP595 Hypertension, Essential 78 0.031
174
P INF038 Influenza 77 0.031
175
LVR012 Liver Cirrhosis 73 0.031
176
ANX010 Anxiety 72 0.031
177
WGN006 Wegener Granulomatosis 71 0.031
178
P ADN016 Adenocarcinoma 71 0.031
179
P MJR001 Major Depressive Disorder 70 0.031
180
P DBT085 Diabetes Mellitus, Insulin-Dependent 69 0.031
181
CNN005 Connective Tissue Disease 65 0.031
182
c GLY008 Glycogen Storage Disease Ii 64 0.031
183
HYP066 Hyperglycemia 64 0.031
184
MSC152 Muscular Dystrophy, Becker Type 64 0.031
185
c TBR025 Tuberous Sclerosis 1 63 0.031
186
P THR005 Thrombotic Thrombocytopenic Purpura 63 0.031
187
P HYP086 Hypothyroidism 62 0.031
188
P GRV001 Graves' Disease 62 0.031
189
P EXN002 Exanthem 62 0.031
190
TNS005 Tonsillitis 61 0.031
191
c SCL052 Scleroderma, Familial Progressive 60 0.031
192
CHL068 Cholestasis 60 0.031
193
MSC165 Muscular Dystrophy, Congenital, Lmna-Related 59 0.031
194
P END033 Endocarditis 58 0.031
195
INF034 Infective Endocarditis 56 0.031
196
FCL014 Focal Epilepsy 56 0.031
197
P MSC003 Muscular Atrophy 55 0.031
198
c FML001 Familial Atrial Fibrillation 55 0.031
199
IMP005 Impotence 54 0.031
200
P EMR001 Emery-Dreifuss Muscular Dystrophy 53 0.031
201
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.031
202
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 53 0.031
203
LDD002 Liddle Syndrome 53 0.031
204
EBS001 Ebstein Anomaly 52 0.031
205
DRG003 Drug Dependence 51 0.031
206
c CNG012 Congenital Generalized Lipodystrophy 51 0.031
207
CCN002 Cocaine Abuse 50 0.031
208
ULN003 Ulnar-Mammary Syndrome 50 0.031
209
MGL038 Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome 48 0.031
210
PNN001 Panniculitis 48 0.031
211
MYC005 Myocardial Stunning 47 0.031
212
AGR002 Agoraphobia 47 0.031
213
c CRD187 Cardiomyopathy, Dilated, 3b 46 0.031
214
HTR003 Heterotaxy 46 0.031
215
P HRT035 Heart Block, Congenital 45 0.031
216
c MYP072 Myopathy, Myofibrillar, 1 44 0.031
217
PHC013 Phaeochromocytoma 44 0.031
218
P LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 43 0.031
219
LYM029 Lymphedema-Distichiasis Syndrome 41 0.031
220
P HYP265 Hypotonia 40 0.031
221
CPL013 Capillary Malformations, Congenital 39 0.031
222
HTR014 Heterotaxy, Visceral, 1, X-Linked 39 0.031
223
ARR045 Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 38 0.031
224
ARR046 Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 38 0.031
225
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.031
226
ARR023 Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 37 0.031
227
THR099 Third-Degree Atrioventricular Block 37 0.031
228
c HMC021 Hemochromatosis, Type 2a 36 0.031
229
INF013 Inferior Myocardial Infarction 36 0.031
230
GST007 Gastric Dilatation 32 0.031
231
SCP009 Scapuloperoneal Myopathy, X-Linked Dominant 32 0.031
232
ANG060 Angiopathy, Hereditary, with Nephropathy, Aneurysms, and Muscle Cramps 30 0.031
233
c EMR017 Emery-Dreifuss Muscular Dystrophy 1, X-Linked 29 0.031
234
MYT003 Myotonic Disease 27 0.031
235
MTC068 Mitochondrial Complex V Deficiency, Nuclear Type 2 27 0.031
236
HSB001 His Bundle Tachycardia 23 0.031
237
ARR027 Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 23 0.031
238
CRD234 Cardiomyopathy, Dilated, 1c, with or Without Left Ventricular Noncompaction 22 0.031
239
c CRD107 Cardiomyopathy, Dilated, 1r 21 0.031
240
HRT018 Heart-Hand Syndrome, Slovenian Type 21 0.031
241
c CRD152 Cardiomyopathy, Familial Hypertrophic, 21 21 0.031
242
c LFT017 Left Ventricular Noncompaction 8 21 0.031
243
MYT026 Myotonia Atrophica 21 0.031
244
ARR024 Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 19 0.031
245
c CRD173 Cardiomyopathy, Dilated, 1nn 19 0.031
246
INT062 Interstitial Myocarditis 19 0.031
247
c LNG046 Long Qt Syndrome 11 18 0.031
248
VNT031 Ventricular Extrasystoles with Syncope, Perodactyly, and Robin Sequence 17 0.031
249
c BRG003 Brugada Syndrome 3 17 0.031
250
ATR076 Atrophic Muscular Disease 6 0.031
251
P HPT023 Hepatocellular Carcinoma 94 0.025
252
P PRS040 Prostate Cancer 88 0.025
253
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.025
254
MYL069 Myeloma, Multiple 86 0.025
255
MLR004 Malaria 86 0.025
256
STR067 Stroke, Ischemic 84 0.025
257
AST005 Asthma 83 0.025
258
ULC004 Ulcerative Colitis 80 0.025
259
P PLM037 Pulmonary Hypertension 79 0.025
260
P NNN008 Noonan Syndrome 1 77 0.025
261
P WSK001 Wiskott-Aldrich Syndrome 76 0.025
262
P LKM002 Leukemia 75 0.025
263
MRF001 Marfan Syndrome 75 0.025
264
P HPT021 Hepatitis 75 0.025
265
P FML018 Familial Mediterranean Fever 73 0.025
266
VNH007 Von Hippel-Lindau Syndrome 72 0.025
267
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.025
268
MLN008 Melanoma 72 0.025
269
KWS002 Kawasaki Disease 72 0.025
270
PRP027 Peripheral Vascular Disease 71 0.025
271
P LYM118 Lymphoma 71 0.025
272
P PNM007 Pneumonia 70 0.025
273
P HRP006 Herpes Simplex 70 0.025
274
WRN001 Werner Syndrome 70 0.025
275
ART016 Aortic Aneurysm 70 0.025
276
P DMN001 Diamond-Blackfan Anemia 70 0.025
277
P MYL006 Myeloid Leukemia 69 0.025
278
c HPT016 Hepatitis B 68 0.025
279
RNL114 Renal Cell Carcinoma, Nonpapillary 68 0.025
280
LYM017 Lyme Disease 68 0.025
281
DMN002 Dementia 68 0.025
282
P HLP001 Holoprosencephaly 67 0.025
283
c EPL184 Epileptic Encephalopathy, Early Infantile, 6 67 0.025
284
P ATT013 Attention Deficit-Hyperactivity Disorder 67 0.025
285
TYP007 Typhoid Fever 67 0.025
286
P KDN017 Kidney Cancer 66 0.025
287
P LYM026 Lymphoblastic Leukemia 66 0.025
288
c LCL006 Localized Scleroderma 66 0.025
289
LGN002 Legionellosis 65 0.025
290
P DRM010 Dermatomyositis 65 0.025
291
P THL005 Thalassemia 65 0.025
292
P ASP006 Aspergillosis 65 0.025
293
TTN003 Tetanus 65 0.025
294
c MLT160 Multiple Endocrine Neoplasia, Type Iia 65 0.025
295
LPT001 Leptospirosis 64 0.025
296
P PNC044 Pancreatitis 64 0.025
297
MTH009 Mouth Disease 64 0.025
298
P HYP802 Hypocalcemia, Autosomal Dominant 1 64 0.025
299
P SRC025 Sarcoidosis 1 63 0.025
300
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 63 0.025
301
DPH001 Diphtheria 63 0.025
302
PRP001 Propionic Acidemia 63 0.025
303
P SPN046 Spinal Muscular Atrophy 63 0.025
304
HMR004 Hemorrhagic Fever with Renal Syndrome 63 0.025
305
CLT003 Colitis 63 0.025
306
YLL002 Yellow Fever 63 0.025
307
P ALC004 Alcohol Abuse 63 0.025
308
GST033 Gestational Diabetes 62 0.025
309
P HML002 Hemolytic Anemia 62 0.025
310
c ACT027 Acute Pancreatitis 61 0.025
311
PRP030 Purpura 61 0.025
312
P DYS154 Dystonia 61 0.025
313
P UVT001 Uveitis 61 0.025
314
MCS002 Mucositis 61 0.025
315
P GLM007 Glomerulonephritis 61 0.025
316
P GLY013 Glycogen Storage Disease 61 0.025
317
P RHB003 Rhabdomyosarcoma 61 0.025
318
P BPL003 Bipolar Disorder 61 0.025
319
MNT002 Mental Depression 60 0.025
320
P MLG056 Malignant Hyperthermia 60 0.025
321
PRP083 Porphyria, Acute Intermittent 60 0.025
322
GT001 Gout 60 0.025
323
DBT010 Diabetic Neuropathy 60 0.025
324
PRS047 Prostatitis 59 0.025
325
RHM001 Rheumatic Fever 59 0.025
326
P MTR012 Mitral Valve Disease 59 0.025
327
URT039 Urticaria 59 0.025
328
PHR003 Pharyngitis 59 0.025
329
LPD008 Lipid Metabolism Disorder 59 0.025
330
STR039 Sturge-Weber Syndrome 59 0.025
331
TRN015 Transient Cerebral Ischemia 58 0.025
332
PTN001 Patent Foramen Ovale 58 0.025
333
MCR088 Microscopic Polyangiitis 58 0.025
334
c PRX045 Peroxisome Biogenesis Disorder 1b 57 0.025
335
P OCL002 Oculocutaneous Albinism 57 0.025
336
P LPD010 Lipodystrophy 57 0.025
337
CYT008 Cytomegalovirus Infection 57 0.025
338
PLM010 Pulmonary Edema 57 0.025
339
P STC001 Stickler Syndrome 56 0.025
340
c ALM001 Al Amyloidosis 56 0.025
341
LYS002 Lysosomal Storage Disease 56 0.025
342
c MYT020 Myotonic Dystrophy 2 56 0.025
343
HYP060 Hyperinsulinism 56 0.025
344
PLS006 Plasmodium Vivax Malaria 56 0.025
345
P MYP006 Myopia 56 0.025
346
DSS009 Disseminated Intravascular Coagulation 56 0.025
347
GST037 Gastroparesis 56 0.025
348
P LMB006 Limb-Girdle Muscular Dystrophy 55 0.025
349
NRT004 Neuritis 55 0.025
350
CHL028 Childhood Type Dermatomyositis 55 0.025
351
DXT001 Dextrocardia 55 0.025
352
MGR028 Migraine with or Without Aura 1 55 0.025
353
P PMP001 Pemphigus 55 0.025
354
P PNM006 Pneumoconiosis 55 0.025
355
INT007 Intermediate Coronary Syndrome 55 0.025
356
TRY001 Trypanosomiasis 55 0.025
357
P HYP014 Hyperuricemia 54 0.025
358
BRN071 Brain Injury 54 0.025
359
SPR004 Supravalvular Aortic Stenosis 54 0.025
360
P SMP003 Simpson-Golabi-Behmel Syndrome 54 0.025
361
CND002 Conduct Disorder 54 0.025
362
P DBT005 Diabetes Insipidus 54 0.025
363
SCH068 Schwartz-Jampel Syndrome, Type 1 54 0.025
364
c ACT071 Acute Kidney Failure 54 0.025
365
GTR002 Goiter 53 0.025
366
PRP019 Peripheral Nervous System Disease 53 0.025
367
LPD009 Lipid Storage Disease 53 0.025
368
THR016 Thrombophlebitis 53 0.025
369
P BRT004 Bartter Disease 52 0.025
370
c CCK007 Cockayne Syndrome B 52 0.025
371
CLC006 Calcinosis 51 0.025
372
RFL001 Reflex Sympathetic Dystrophy 51 0.025
373
THY030 Thyroid Gland Disease 51 0.025
374
EHL034 Ehlers-Danlos Syndrome, Hypermobility Type 51 0.025
375
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 51 0.025
376
PLR001 Pleural Tuberculosis 50 0.025
377
EXP004 Exophthalmos 50 0.025
378
P PSD015 Pseudohypoparathyroidism 50 0.025
379
HND002 Hand, Foot and Mouth Disease 50 0.025
380
ESN011 Eisenmenger Syndrome 49 0.025
381
PRP007 Priapism 49 0.025
382
NNN026 Noonan Syndrome with Multiple Lentigines 49 0.025
383
MTB004 Metabolic Acidosis 49 0.025
384
ANX004 Anoxia 49 0.025
385
c CCK008 Cockayne Syndrome a 48 0.025
386
SPH010 Sphingolipidosis 48 0.025
387
HDN002 Head Injury 48 0.025
388
ART004 Aortic Atherosclerosis 48 0.025
389
c BRN108 Branchiootic Syndrome 1 47 0.025
390
c HYP805 Hypercholesterolemia, Autosomal Dominant, 3 47 0.025
391
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 47 0.025
392
CRN295 Carnitine Palmitoyltransferase I Deficiency 46 0.025
393
c PRG126 Progressive Familial Heart Block 46 0.025
394
P MTH007 Methemoglobinemia 46 0.025
395
PMP004 Pemphigus Foliaceus 46 0.025
396
DDN006 Duodenitis 46 0.025
397
ANH002 Anhidrosis 45 0.025
398
ALB002 Albinism 45 0.025
399
MNN032 Meningococcal Meningitis 45 0.025
400
c MSC050 Muscular Dystrophy, Congenital, 1b 45 0.025
401
MCL009 Mcleod Syndrome 45 0.025
402
STR089 Storage Pool Platelet Disease 43 0.025
403
c EMR018 Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant 43 0.025
404
PLM068 Pulmonary Vein Stenosis 43 0.025
405
NRN002 Neuronitis 43 0.025
406
MNN017 Mononeuropathy 42 0.025
407
SCT001 Sciatic Neuropathy 41 0.025
408
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 41 0.025
409
DBT090 Diabetes and Deafness, Maternally Inherited 40 0.025
410
c HMC035 Hemochromatosis, Type 4 40 0.025
411
TRN012 Transient Global Amnesia 40 0.025
412
ADN002 Adenoiditis 40 0.025
413
c SPL067 Split-Hand/foot Malformation 1 40 0.025
414
WBR001 Weber Syndrome 40 0.025
415
ANT018 Anthracosis 39 0.025
416
P HYP599 Hypoparathyroidism, Familial Isolated 39 0.025
417
PHS004 Phosphoribosylpyrophosphate Synthetase Superactivity 39 0.025
418
PRL008 Paralytic Ileus 38 0.025
419
c MLG147 Malignant Hyperthermia 1 38 0.025
420
c CRD104 Cardiomyopathy, Dilated, 1p 38 0.025
421
ALC010 Alcoholic Cardiomyopathy 38 0.025
422
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 37 0.025
423
HYP022 Hypohidrosis 36 0.025
424
HMN035 Hemangioma-Thrombocytopenia Syndrome 36 0.025
425
CRD229 Cardiomyopathy, Dilated, with Hypergonadotropic Hypogonadism 36 0.025
426
P MYC026 Myoclonus Epilepsy 35 0.025
427
URT037 Urethral Stricture 35 0.025
428
ARR050 Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 35 0.025
429
c MTR080 Mitral Valve Prolapse 1 34 0.025
430
GLS004 Glossopharyngeal Neuralgia 34 0.025
431
RHM035 Rheumatic Fever-Related Antigen 34 0.025
432
CHR543 Chromosome 2q37 Deletion Syndrome 34 0.025
433
P ATR081 Atrial Standstill 34 0.025
434
c BRG007 Brugada Syndrome 5 33 0.025
435
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.025
436
c FML250 Familial Progressive Cardiac Conduction Defect 33 0.025
437
P HRT017 Heart Tumor 32 0.025
438
PRG023 Progeroid Short Stature with Pigmented Nevi 32 0.025
439
c CTS034 Cutis Laxa, Autosomal Recessive Type 1 32 0.025
440
PRP066 Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease 32 0.025
441
DFN007 Deafness Enamel Hypoplasia Nail Defects 32 0.025
442
P EHL081 Ehlers-Danlos Syndrome, Classic-Like 31 0.025
443
BRK012 Broken Heart Syndrome 31 0.025
444
PST048 Postural Orthostatic Tachycardia Syndrome 31 0.025
445
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.025
446
ALR002 Al-Raqad Syndrome 30 0.025
447
c ATM068 Autoimmune Hypoparathyroidism 30 0.025
448
P EMR004 Emery-Dreifuss Muscular Dystrophy, X-Linked 29 0.025
449
IVC001 Ivic Syndrome 29 0.025
450
SCN049 Second-Degree Atrioventricular Block 29 0.025
451
BRN055 Bronchogenic Cyst 28 0.025
452
HYP682 Hypertelorism, Teebi Type 26 0.025
453
MTC088 Mitochondrial Dna Depletion Syndrome 13 26 0.025
454
SLH001 Salih Myopathy 26 0.025
455
ARR048 Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 26 0.025
456
SHP003 Shapiro Syndrome 26 0.025
457
c BRG006 Brugada Syndrome 2 25 0.025
458
WLD006 Wild Type Abeta2m Amyloidosis 25 0.025
459
c PLM121 Pulmonary Hypertension, Primary, 4 25 0.025
460
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 24 0.025
461
MYP056 Myopathy, X-Linked, with Postural Muscle Atrophy 24 0.025
462
CLC053 Colchicine Poisoning 24 0.025
463
CHR586 Chromosome 16p12.2-P11.2 Deletion Syndrome, 7.1- to 8.7-Mb 24 0.025
464
c CRD091 Cardiomyopathy, Dilated, 1dd 24 0.025
465
BLD163 Blood Group, Dombrock System 23 0.025
466
c CRD056 Cardiomyopathy, Familial Hypertrophic, 11 23 0.025
467
HRY002 Hairy Tongue 22 0.025
468
HRT038 Heart, Malformation of 22 0.025
469
c DYS145 Dystonia 23 22 0.025
470
MTC078 Mitochondrial Dna Depletion Syndrome 11 22 0.025
471
CMB054 Combined Oxidative Phosphorylation Deficiency 23 22 0.025
472
CRD237 Cardiomyopathy, Dilated, 1aa, with or Without Left Ventricular Noncompaction 22 0.025
473
CMB025 Combined Oxidative Phosphorylation Deficiency 10 21 0.025
474
c VNT028 Ventricular Septal Defect 1 21 0.025
475
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.025
476
CRD023 Cardiomyopathy Cataract Hip Spine Disease 21 0.025
477
NTH002 Nathalie Syndrome 21 0.025
478
HYD050 Hydrocephalus, Endocardial Fibroelastosis, and Cataracts 20 0.025
479
SBR011 Subaortic Stenosis--Short Stature Syndrome 20 0.025
480
P PHC014 Phocomelia 20 0.025
481
ARR028 Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 19 0.025
482
TBT001 Tabatznik Syndrome 19 0.025
483
CTN032 Cutaneous Mastocytosis, Conductive Hearing Loss and Microtia 19 0.025
484
BLC017 Black Hairy Tongue 19 0.025
485
19P001 19p13.12 Microdeletion Syndrome 18 0.025
486
ARR041 Arrhythmogenic Right Ventricular Dysplasia, Familial, 13 18 0.025
487
WLL032 Woolly Hair, Hypotrichosis, Everted Lower Lip, and Outstanding Ears 18 0.025
488
c BRG009 Brugada Syndrome 7 18 0.025
489
c VNT024 Ventricular Septal Defect 3 18 0.025
490
c EMR015 Emery-Dreifuss Muscular Dystrophy 5, Autosomal Dominant 18 0.025
491
SYM006 Symmetrical Thalamic Calcifications 18 0.025
492
ECT023 Ectodermal Dysplasia, Hidrotic, Christianson-Fourie Type 17 0.025
493
PLY088 Polyvalvular Heart Disease Syndrome 17 0.025
494
c BRG012 Brugada Syndrome 9 17 0.025
495
c BRG008 Brugada Syndrome 6 17 0.025
496
HRS003 Hirschsprung Disease Ganglioneuroblastoma 17 0.025
497
c BRG010 Brugada Syndrome 8 16 0.025
498
MTR030 Mitral Valve Prolapse, Familial, X-Linked 16 0.025
499
c BRG004 Brugada Syndrome 4 16 0.025
500
PLY127 Polyneuropathy-Intellectual Disability-Acromicria-Premature Menopause Syndrome 16 0.025
501
ARR047 Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 16 0.025
502
c VNT026 Ventricular Septal Defect 2 16 0.025
503
MSC030 Muscular Fibrosis Multifocal Obstructed Vessels 14 0.025
504
CHT001 Chaotic Atrial Tachycardia 12 0.025
505
MSC156 Muscular Dystrophy, Progressive Pectorodorsal 10 0.025
506
TRS022 Torsade De Pointes, Short-Coupled Variant 7 0.025
507
P BRS047 Breast Cancer 100 0.018
508
P LNG032 Lung Cancer 99 0.018
509
P CLR023 Colorectal Cancer 98 0.018
510
P ALZ034 Alzheimer Disease 95 0.018
511
P RHM011 Rheumatoid Arthritis 91 0.018
512
P PNC035 Pancreatic Cancer 89 0.018
513
OST012 Osteoarthritis 88 0.018
514
P MLT020 Multiple Sclerosis 85 0.018
515
CYS001 Cystic Fibrosis 85 0.018
516
GST053 Gastric Cancer 84 0.018
517
INS024 Insulin-Like Growth Factor I 83 0.018
518
P OVR042 Ovarian Cancer 82 0.018
519
c LKM061 Leukemia, Acute Myeloid 81 0.018
520
CRH001 Crohn's Disease 80 0.018
521
c LKM063 Leukemia, Chronic Myeloid 80 0.018
522
ESP021 Esophageal Cancer 79 0.018
523
c MCL042 Macular Degeneration, Age-Related, 1 79 0.018
524
LYM133 Lymphoma, Hodgkin, Classic 78 0.018
525
P PRK057 Parkinson Disease, Late-Onset 78 0.018
526
P BLD134 Bladder Cancer 78 0.018
527
P HNT016 Huntington Disease 78 0.018
528
P ART022 Arthritis 77 0.018
529
P RTN024 Retinoblastoma 76 0.018
530
P LVR013 Liver Disease 76 0.018
531
MNT001 Mantle Cell Lymphoma 76 0.018
532
P MYL005 Myelofibrosis 75 0.018
533
PLY001 Polycythemia Vera 75 0.018
534
P OST002 Osteoporosis 75 0.018
535
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.018
536
c LKM071 Leukemia, Chronic Lymphocytic 75 0.018
537
MYL009 Myelodysplastic Syndrome 75 0.018
538
SQM006 Squamous Cell Carcinoma 74 0.018
539
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.018
540
GLB002 Glioblastoma 74 0.018
541
APL001 Aplastic Anemia 74 0.018
542
KPS004 Kaposi Sarcoma 73 0.018
543
PHN003 Phenylketonuria 73 0.018
544
c HPT073 Hepatitis C Virus 73 0.018
545
SCK003 Sickle Cell Anemia 73 0.018
546
c HPT001 Hepatitis C 73 0.018
547
P NRB001 Neuroblastoma 73 0.018
548
PLM134 Pulmonary Fibrosis, Idiopathic 73 0.018
549
PLM001 Pulmonary Tuberculosis 72 0.018
550
PSY004 Psychotic Disorder 72 0.018
551
THY028 Thyroid Cancer 72 0.018
552
P CRV035 Cervical Cancer 72 0.018
553
P PHC003 Pheochromocytoma 72 0.018
554
BRN028 Brain Cancer 72 0.018
555
NRF026 Neurofibromatosis, Type Iv, of Riccardi 72 0.018
556
LSH001 Leishmaniasis 71 0.018
557
P END044 Endometriosis 71 0.018
558
SVR004 Severe Combined Immunodeficiency 71 0.018
559
c SPN225 Spondyloarthropathy 1 71 0.018
560
HMN044 Human Immunodeficiency Virus Type 1 71 0.018
561
P SCH015 Schizophrenia 71 0.018
562
BRC012 Brucellosis 71 0.018
563
P ESS003 Essential Thrombocythemia 71 0.018
564
LYM143 Lymphoma, Non-Hodgkin, Familial 71 0.018
565
CRZ001 Crouzon Syndrome 71 0.018
566
CNN003 Conn's Syndrome 70 0.018
567
OST159 Osteogenic Sarcoma 70 0.018
568
P AGM001 Agammaglobulinemia 70 0.018
569
CRB037 Cerebral Palsy 70 0.018
570
P BCL006 B-Cell Lymphomas 70 0.018
571
PRT037 Pertussis 70 0.018
572
P LPS004 Lupus Erythematosus 69 0.018
573
P NRF023 Neurofibromatosis, Type Ii 69 0.018
574
P TBR001 Tuberous Sclerosis 69 0.018
575
P DRM053 Dermatitis, Atopic 68 0.018
576
P PLM036 Pulmonary Fibrosis 68 0.018
577
GLB015 Glioblastoma Multiforme 68 0.018
578
P PLZ001 Pelizaeus-Merzbacher Disease 68 0.018
579
ALL003 Allergic Rhinitis 68 0.018
580
OBS002 Obsessive-Compulsive Disorder 68 0.018
581
c ATS007 Autism Spectrum Disorder 68 0.018
582
P ALG028 Alagille Syndrome 1 68 0.018
583
P HYD006 Hydrocephalus 68 0.018
584
SRC014 Sarcoma 68 0.018
585
SKN016 Skin Disease 68 0.018
586
P ART023 Arthropathy 68 0.018
587
P CHR071 Charcot-Marie-Tooth Disease 67 0.018
588
P ADL010 Adult Respiratory Distress Syndrome 67 0.018
589
P HMP002 Hemophagocytic Lymphohistiocytosis 67 0.018
590
P MCL013 Mucolipidosis Iv 67 0.018
591
OTT002 Otitis Media 67 0.018
592
BRN024 Bronchitis 67 0.018
593
c PLM164 Pulmonary Hypertension, Primary, 1 67 0.018
594
P PRD008 Periodontitis 67 0.018
595
P TMP003 Temporal Arteritis 67 0.018
596
DRM006 Dermatitis 67 0.018
597
BRS051 Breast Disease 67 0.018
598
PRT036 Peritonitis 67 0.018
599
DNG002 Dengue Hemorrhagic Fever 66 0.018
600
P AST007 Astrocytoma 66 0.018
601
ATM095 Autoimmune Disease 66 0.018
602
P MCR115 Microvascular Complications of Diabetes 5 66 0.018
603
P PRD006 Prader-Willi Syndrome 66 0.018
604
c BSL007 Basal Cell Carcinoma 66 0.018
605
MXD005 Mixed Connective Tissue Disease 66 0.018
606
P ENC004 Encephalitis 66 0.018
607
VSC011 Vasculitis 66 0.018
608
PSR001 Psoriatic Arthritis 66 0.018
609
GST050 Gastrointestinal System Disease 66 0.018
610
CTN007 Cutaneous Leishmaniasis 66 0.018
611
ACQ007 Acquired Immunodeficiency Syndrome 65 0.018
612
c EXD008 Exudative Vitreoretinopathy 1 65 0.018
613
P CRN015 Cornelia De Lange Syndrome 65 0.018
614
GST045 Gastroenteritis 65 0.018
615
MLT157 Multiple System Atrophy 1 65 0.018
616
P INT068 Intestinal Disease 65 0.018
617
P PSR002 Psoriasis 65 0.018
618
c PRC016 Pre-Eclampsia 65 0.018
619
NRF007 Neurofibroma 65 0.018
620
P THR014 Thrombocytopenia 65 0.018
621
SCR008 Scrub Typhus 65 0.018
622
P PRS038 Personality Disorder 65 0.018
623
P ART067 Aortic Aneurysm, Familial Thoracic 1 65 0.018
624
CNT097 Central Hypoventilation Syndrome, Congenital 65 0.018
625
ALC007 Alcohol Dependence 65 0.018
626
MDD011 Mood Disorder 64 0.018
627
DFF005 Diffuse Large B-Cell Lymphoma 64 0.018
628
VRC005 Varicose Veins 64 0.018
629
P GLL020 Gallbladder Disease 64 0.018
630
MYL031 Myeloproliferative Neoplasm 64 0.018
631
INC002 Inclusion Body Myositis 64 0.018
632
PRD007 Periodontal Disease 64 0.018
633
VRL011 Viral Infectious Disease 64 0.018
634
CRP001 Carpal Tunnel Syndrome 64 0.018
635
ART005 Arteriovenous Malformation 64 0.018
636
P ALP009 Alopecia Areata 64 0.018
637
SVR097 Severe Cutaneous Adverse Reaction 64 0.018
638
GNG013 Gingivitis 64 0.018
639
GST092 Gastroesophageal Reflux 64 0.018
640
P ESP024 Esophagitis 64 0.018
641
HMT002 Hematologic Cancer 64 0.018
642
P NRC002 Narcolepsy 64 0.018
643
IMM174 Immunodeficiency with Hyper-Igm, Type 1 64 0.018
644
CMB081 Combined Immunodeficiency, X-Linked 64 0.018
645
BRR014 Barrett Esophagus 64 0.018
646
MST017 Mast Cell Disease 63 0.018
647
ADN018 Adenoma 63 0.018
648
c HPT003 Hepatitis a 63 0.018
649
PNC033 Pancreas Adenocarcinoma 63 0.018
650
P INT143 Interstitial Cystitis 63 0.018
651
KRT001 Keratoconjunctivitis Sicca 63 0.018
652
c ACT210 Acute Respiratory Distress Syndrome 63 0.018
653
CRN036 Craniopharyngioma 63 0.018
654
c ADL017 Adult T-Cell Leukemia 63 0.018
655
P MYS005 Myositis 63 0.018
656
P PLV020 Pelvic Organ Prolapse 63 0.018
657
SKN019 Skin Melanoma 63 0.018
658
P LYM025 Lymphedema 63 0.018
659
IRR002 Irritable Bowel Syndrome 63 0.018
660
P HYP055 Hypoplastic Left Heart Syndrome 63 0.018
661
INT066 Interstitial Lung Disease 63 0.018
662
P SNS014 Sinusitis 62 0.018
663
P HRM001 Hermansky-Pudlak Syndrome 62 0.018
664
RHM027 Rheumatic Disease 62 0.018
665
IMM167 Immune Deficiency Disease 62 0.018
666
P CTS001 Cutis Laxa 62 0.018
667
VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 62 0.018
668
P PRP029 Porphyria 62 0.018
669
PLM033 Pulmonary Embolism 62 0.018
670
ALC006 Alcoholic Hepatitis 62 0.018
671
CMM005 Common Cold 62 0.018
672
FLL027 Fallopian Tube Carcinoma 62 0.018
673
MTR014 Motor Neuron Disease 62 0.018
674
P CMR001 Camurati-Engelmann Disease 62 0.018
675
P RHN004 Rhinitis 62 0.018
676
c CNG006 Congenital Hypothyroidism 62 0.018
677
P MTR004 Maturity-Onset Diabetes of the Young 62 0.018
678
FTT001 Fatty Liver Disease 62 0.018
679
c MCR129 Microvascular Complications of Diabetes 1 62 0.018
680
GTL001 Gitelman Syndrome 62 0.018
681
P AGN002 Agnosia 61 0.018
682
NRV006 Nervous System Cancer 61 0.018
683
P LPS002 Liposarcoma 61 0.018
684
P EHL001 Ehlers-Danlos Syndrome 61 0.018
685
SYN007 Synovitis 61 0.018
686
INT002 Intermittent Claudication 61 0.018
687
MRB003 Morbid Obesity 61 0.018
688
STF001 Stiff-Person Syndrome 61 0.018
689
TXC005 Toxic Shock Syndrome 61 0.018
690
P HMN010 Hemangioma 61 0.018
691
LMY014 Leiomyoma, Uterine 61 0.018
692
P HMR003 Hemorrhagic Disease 61 0.018
693
OCL009 Ocular Cancer 61 0.018
694
c THR092 Thrombophilia Due to Thrombin Defect 61 0.018
695
QFV001 Q Fever 61 0.018
696
HRP004 Herpes Zoster 61 0.018
697
P SPN052 Spondyloarthropathy 61 0.018
698
P GLM045 Glioma 61 0.018
699
ALL006 Allergic Asthma 60 0.018
700
P CTR002 Cataract 60 0.018
701
IDP011 Idiopathic Interstitial Pneumonia 60 0.018
702
KLP010 Klippel-Trenaunay-Weber Syndrome 60 0.018
703
P GST049 Gastrointestinal System Cancer 60 0.018
704
c ALP101 Alpha-Thalassemia 60 0.018
705
STT001 Status Epilepticus 60 0.018
706
ALP103 Alpha-1-Antitrypsin Deficiency 60 0.018
707
PRT058 Pure Autonomic Failure 60 0.018
708
JNT002 Joint Disorders 60 0.018
709
P HYP040 Hypospadias 60 0.018
710
TRG002 Trigeminal Neuralgia 60 0.018
711
P HMR012 Hemorrhagic Fever 60 0.018
712
SPN027 Spinal Stenosis 60 0.018
713
HRY003 Hairy Cell Leukemia 60 0.018
714
P FCL005 Focal Segmental Glomerulosclerosis 60 0.018
715
P PLY018 Polycythemia 60 0.018
716
ERY003 Erythema Multiforme 60 0.018
717
BRN002 Bronchiolitis 59 0.018
718
c PRM126 Primary Peritoneal Carcinoma 59 0.018
719
P INF032 Infertility 59 0.018
720
c VRL010 Viral Hepatitis 59 0.018
721
RGD003 Rigid Spine Muscular Dystrophy 1 59 0.018
722
P PRT013 Portal Hypertension 59 0.018
723
PST028 Post-Traumatic Stress Disorder 59 0.018
724
c HRD002 Hereditary Angioedema 59 0.018
725
c PRM005 Primary Hyperparathyroidism 59 0.018
726
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 59 0.018
727
DBT062 Diabetic Foot Ulcers 59 0.018
728
SNS001 Sensorineural Hearing Loss 59 0.018
729
TRD006 Tardive Dyskinesia 59 0.018
730
P PLM034 Pulmonary Emphysema 59 0.018
731
HPT019 Hepatic Encephalopathy 59 0.018
732
RTN017 Retinal Detachment 59 0.018
733
ING001 Inguinal Hernia 59 0.018
734
P LMY004 Leiomyosarcoma 59 0.018
735
P OLG002 Oligodendroglioma 59 0.018
736
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.018
737
PNC034 Pancreas Disease 59 0.018
738
c FCL025 Focal Segmental Glomerulosclerosis 1 59 0.018
739
ICH054 Ichthyosis, X-Linked 59 0.018
740
BNC003 Bone Cancer 59 0.018
741
P HYP083 Hypopituitarism 59 0.018
742
CHL067 Cholecystitis 58 0.018
743
P HYP069 Hyperparathyroidism 58 0.018
744
c ESS001 Essential Tremor 58 0.018
745
P INT030 Intracranial Aneurysm 58 0.018
746
SFT003 Soft Tissue Sarcoma 58 0.018
747
LMY002 Leiomyoma 58 0.018
748
CRT016 Carotid Artery Disease 58 0.018
749
CMP010 Complex Regional Pain Syndrome 58 0.018
750
NRN004 Neuroendocrine Tumor 58 0.018
751
VSC002 Vascular Dementia 58 0.018
752
P OVR049 Ovarian Disease 58 0.018
753
P LTR001 Lateral Sclerosis 58 0.018
754
DMY004 Demyelinating Disease 58 0.018
755
HMT018 Hematopoietic Stem Cell Transplantation 58 0.018
756
c GLC092 Glaucoma, Primary Open Angle 58 0.018
757
BRN038 Bronchial Disease 58 0.018
758
P THR015 Thrombophilia 58 0.018
759
INT146 Intervertebral Disc Disease 58 0.018
760
LYM019 Lymphosarcoma 58 0.018
761
RSC001 Rosacea 58 0.018
762
GLC003 Glucose Intolerance 58 0.018
763
ESP023 Esophageal Disease 58 0.018
764
P DST002 Distal Arthrogryposis 57 0.018
765
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 57 0.018
766
ART017 Aortic Disease 57 0.018
767
THR100 Thrombocytopenic Purpura, Autoimmune 57 0.018
768
P ECL001 Eclampsia 57 0.018
769
P SBS003 Substance Abuse 57 0.018
770
HMR039 Hemorrhage, Intracerebral 57 0.018
771
ANG020 Angiosarcoma 57 0.018
772
P PRG013 Paraganglioma 57 0.018
773
IMM158 Immune Suppression 57 0.018
774
BRN004 Brain Edema 57 0.018
775
P MCR010 Microcephaly 57 0.018
776
P CYS018 Cystitis 57 0.018
777
ADN027 Adenomyosis 57 0.018
778
CNS004 Constipation 57 0.018
779
CLR003 Clear Cell Adenocarcinoma 57 0.018
780
P PNC025 Panic Disorder 57 0.018
781
P ANG015 Angioedema 57 0.018
782
IMM136 Immune System Disease 57 0.018
783
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 57 0.018
784
c EPS042 Episodic Ataxia, Type 1 57 0.018
785
MSC007 Muscle Hypertrophy 57 0.018
786
SPT005 Spotted Fever 57 0.018
787
NPH009 Nephrolithiasis 57 0.018
788
LBR002 Leber Hereditary Optic Neuropathy 57 0.018
789
CYS005 Cysticercosis 57 0.018
790
P HYP726 Hypercalcemia, Infantile, 1 57 0.018
791
PNM008 Pneumothorax 57 0.018
792
NWB001 Newborn Respiratory Distress Syndrome 56 0.018
793
P FCS012 Facioscapulohumeral Muscular Dystrophy 1 56 0.018
794
P BRN009 Burning Mouth Syndrome 56 0.018
795
RTN018 Retinal Disease 56 0.018
796
c ANM038 Anemia, Autoimmune Hemolytic 56 0.018
797
NNL002 Nonalcoholic Steatohepatitis 56 0.018
798
P SCL018 Scoliosis 56 0.018
799
P CPL006 Capillary Hemangioma 56 0.018
800
P ATR001 Atrioventricular Septal Defect 56 0.018
801
P EHL052 Ehlers-Danlos Syndrome, Vascular Type 56 0.018
802
c FML116 Familial Cold Autoinflammatory Syndrome 1 56 0.018
803
BNF002 Bone Fracture 56 0.018
804
PRS042 Prostate Disease 56 0.018
805
BLR001 Biliary Atresia 56 0.018
806
P CTN015 Cutaneous T Cell Lymphoma 56 0.018
807
c INS002 in Situ Carcinoma 56 0.018
808
PRN019 Perinatal Necrotizing Enterocolitis 56 0.018
809
P RTN016 Retinal Degeneration 56 0.018
810
P ACT008 Actinic Keratosis 56 0.018
811
MYM001 Myoma 56 0.018
812
P THY032 Thyroiditis 56 0.018
813
ESN005 Eosinophilic Gastroenteritis 56 0.018
814
PRV006 Pervasive Developmental Disorder 56 0.018
815
P MGR003 Migraine with Aura 56 0.018
816
P CHL002 Childhood Absence Epilepsy 56 0.018
817
c CHR320 Chiari Malformation Type I 56 0.018
818
MTH078 Methylmalonic Aciduria, Cblb Type 56 0.018
819
EXF001 Exfoliation Syndrome 55 0.018
820
RDC002 Radiculopathy 55 0.018
821
BLD044 Bladder Disease 55 0.018
822
SMT006 Somatoform Disorder 55 0.018
823
P INT070 Intestinal Obstruction 55 0.018
824
P ESP035 Esophagitis, Eosinophilic, 1 55 0.018
825
CLN019 Colonic Disease 55 0.018
826
SPN051 Spondylitis 55 0.018
827
HDC001 Headache 55 0.018
828
PNM001 Pneumocystosis 55 0.018
829
P MMB011 Membranous Nephropathy 55 0.018
830
P UTR058 Uterine Anomalies 55 0.018
831
THR004 Thrombocytosis 55 0.018
832
DGN001 Degenerative Disc Disease 55 0.018
833
STR020 Strabismus 55 0.018
834
MTC027 Mitochondrial Trifunctional Protein Deficiency 55 0.018
835
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.018
836
SRS001 Serous Cystadenocarcinoma 55 0.018
837
PRC013 Pericarditis 55 0.018
838
P SYP003 Syphilis 55 0.018
839
c LYM130 Lymphedema, Hereditary, Ii 55 0.018
840
TXC002 Toxic Encephalopathy 55 0.018
841
P HYP024 Hypoparathyroidism 55 0.018
842
TBC004 Tobacco Addiction 55 0.018
843
c GLY004 Glycogen Storage Disease V 55 0.018
844
P FML052 Familial Cold Autoinflammatory Syndrome 55 0.018
845
BLR006 Biliary Tract Disease 55 0.018
846
CPR004 Coproporphyria, Hereditary 54 0.018
847
TRM010 Traumatic Brain Injury 54 0.018
848
TTH006 Tooth Disease 54 0.018
849
P TRC086 Trichohepatoenteric Syndrome 1 54 0.018
850
DYS014 Dyspepsia 54 0.018
851
c OVR114 Ovarian Cancer 1 54 0.018
852
PST021 Postpartum Depression 54 0.018
853
RHM028 Rheumatic Heart Disease 54 0.018
854
SCK005 Sickle Cell Disease 54 0.018
855
PLR022 Pleural Disease 54 0.018
856
TCD001 Tic Disorder 54 0.018
857
c INF071 Inflammatory Bowel Disease 1 54 0.018
858
P TRM003 Tremor 54 0.018
859
MCN001 Mucinous Adenocarcinoma 54 0.018
860
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 54 0.018
861
OPT003 Opiate Dependence 54 0.018
862
c PYR010 Peyronie's Disease 54 0.018
863
ADR013 Adrenal Gland Hyperfunction 54 0.018
864
PRP080 Peripheral Artery Disease 54 0.018
865
HMP005 Hemiplegia 54 0.018
866
TMP001 Temporal Lobe Epilepsy 54 0.018
867
SPN041 Spinal Cord Disease 54 0.018
868
RST001 Restless Legs Syndrome 54 0.018
869
QDR001 Quadriplegia 54 0.018
870
P HMG032 Hemoglobin H Disease 53 0.018
871
CLC001 Calciphylaxis 53 0.018
872
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.018
873
OVR063 Overnutrition 53 0.018
874
P VNS003 Venous Insufficiency 53 0.018
875
P CLL015 Collagen Disease 53 0.018
876
RCT018 Rectal Neoplasm 53 0.018
877
GNR004 Generalized Anxiety Disorder 53 0.018
878
LGN001 Legionnaires' Disease 53 0.018
879
c SPH013 Spherocytosis, Type 1 53 0.018
880
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 53 0.018
881
ANG054 Angina Pectoris 53 0.018
882
P MTC133 Mitochondrial Myopathy 53 0.018
883
c SVR005 Severe Pre-Eclampsia 53 0.018
884
RSS026 Roussy-Levy Hereditary Areflexic Dystasia 53 0.018
885
P RTN022 Retinal Vein Occlusion 53 0.018
886
CLL003 Cellulitis 53 0.018
887
P CTN003 Cutaneous Lupus Erythematosus 53 0.018
888
INT075 Intracranial Hypertension 53 0.018
889
P TRN034 Transverse Myelitis 53 0.018
890
KRT009 Keratosis 53 0.018
891
HMG005 Hemoglobinopathy 53 0.018
892
OPT006 Optic Nerve Disease 53 0.018
893
NDL013 Nodular Regenerative Hyperplasia 53 0.018
894
CLN015 Colon Adenocarcinoma 53 0.018
895
RTN015 Retinal Cancer 53 0.018
896
HLL004 Hellp Syndrome 53 0.018
897
ALC009 Alcoholic Liver Cirrhosis 53 0.018
898
PRV004 Periventricular Leukomalacia 53 0.018
899
c PRM012 Primary Polycythemia 53 0.018
900
END040 Endogenous Depression 53 0.018
901
P HRD018 Hair Disease 53 0.018
902
P PNV001 Panuveitis 52 0.018
903
STM007 Stomatitis 52 0.018
904
c PNS012 Paine Syndrome 52 0.018
905
c PSD066 Pseudohypoparathyroidism, Type Ib 52 0.018
906
PST095 Post-Thrombotic Syndrome 52 0.018
907
ENT011 Enterocolitis 52 0.018
908
ADN001 Adenosine Deaminase Deficiency 52 0.018
909
VTM028 Vitamin E, Familial Isolated Deficiency of 52 0.018
910
LNT004 Lentigines 52 0.018
911
ILT001 Ileitis 52 0.018
912
CRT013 Carotid Stenosis 52 0.018
913
BLD036 Bile Duct Disease 52 0.018
914
IGG001 Iga Glomerulonephritis 52 0.018
915
P INF037 Inflammatory Bowel Disease 52 0.018
916
STM006 Stomach Disease 52 0.018
917
P CHL066 Cholangitis 52 0.018
918
TLN003 Telangiectasis 52 0.018
919
STT041 Stuttering 52 0.018
920
P SHR001 Short Bowel Syndrome 52 0.018
921
INN002 Inner Ear Disease 52 0.018
922
CHR005 Chorioamnionitis 52 0.018
923
CCN001 Cocaine Dependence 52 0.018
924
MTN003 Motion Sickness 52 0.018
925
MYL001 Myelitis 52 0.018
926
OST016 Osteochondrosis 52 0.018
927
VPM001 Vipoma 52 0.018
928
P CHR345 Chronic Pain 52 0.018
929
CRV040 Cervix Carcinoma 52 0.018
930
SPN020 Spondylosis 52 0.018
931
c GRV008 Graves Disease 1 52 0.018
932
DBT004 Diabetic Polyneuropathy 51 0.018
933
PRN021 Paranasal Sinus Disease 51 0.018
934
P RNL007 Renal Tubular Acidosis 51 0.018
935
END021 Endomyocardial Fibrosis 51 0.018
936
OCL006 Ocular Hypertension 51 0.018
937
DRY001 Dry Eye Syndrome 51 0.018
938
MCL006 Macular Retinal Edema 51 0.018
939
P RST002 Restrictive Cardiomyopathy 51 0.018
940
P PLY017 Polyarteritis Nodosa 51 0.018
941
NPH091 Nephrolithiasis, Calcium Oxalate 51 0.018
942
ATN002 Autonomic Nervous System Disease 51 0.018
943
BBS001 Babesiosis 51 0.018
944
NRM004 Neuroma 51 0.018
945
c INV001 Invasive Aspergillosis 51 0.018
946
SRT004 Serotonin Syndrome 51 0.018
947
SCH012 Schizoaffective Disorder 51 0.018
948
c GLC097 Glaucoma 3, Primary Congenital, a 51 0.018
949
ADR012 Adrenal Gland Disease 51 0.018
950
PLS009 Plasma Cell Neoplasm 51 0.018
951
BRX001 Bruxism 51 0.018
952
c MLG074 Malignant Mesenchymoma 51 0.018
953
SBS004 Substance Dependence 51 0.018
954
RTC009 Reticulum Cell Sarcoma 51 0.018
955
NSD001 Nose Disease 51 0.018
956
DSS008 Disease of Mental Health 51 0.018
957
P END046 Endometritis 51 0.018
958
P OPN001 Open-Angle Glaucoma 51 0.018
959
INT067 Interstitial Nephritis 51 0.018
960
CYS014 Cystadenocarcinoma 51 0.018
961
P LCT001 Lactic Acidosis 51 0.018
962
P HMR005 Hemorrhoid 51 0.018
963
c ART115 Aortic Valve Disease 1 51 0.018
964
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 51 0.018
965
P END047 Endophthalmitis 51 0.018
966
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 51 0.018
967
CHL004 Cholelithiasis 51 0.018
968
MSC162 Muscular Dystrophy, Congenital Merosin-Deficient, 1a 51 0.018
969
PRT082 Preterm Premature Rupture of the Membranes 51 0.018
970
c MYP132 Myopathy, Congenital 51 0.018
971
FCL012 Facial Paralysis 50 0.018
972
SHH001 Sheehan Syndrome 50 0.018
973
KLD001 Keloids 50 0.018
974
DNT012 Dental Caries 50 0.018
975
ACT017 Acute Chest Syndrome 50 0.018
976
PRT018 Portal Vein Thrombosis 50 0.018
977
FLL008 Folliculitis 50 0.018
978
HMN032 Human Herpesvirus 8 50 0.018
979
HYD012 Hydrops Fetalis 50 0.018
980
GNG011 Gingival Disease 50 0.018
981
P HMC002 Homocystinuria 50 0.018
982
PNC001 Pancytopenia 50 0.018
983
P HML001 Hemolytic-Uremic Syndrome 50 0.018
984
PLP001 Pulpitis 50 0.018
985
P PTS002 Ptosis 50 0.018
986
c RBN021 Rubinstein-Taybi Syndrome 1 50 0.018
987
SCL003 Social Phobia 50 0.018
988
PLC007 Placental Abruption 50 0.018
989
c RTN162 Retinitis Pigmentosa 2 50 0.018
990
ANG018 Angiomyolipoma 50 0.018
991
c CNT016 Central Retinal Vein Occlusion 50 0.018
992
URT031 Ureteral Disease 50 0.018
993
THR013 Thoracic Outlet Syndrome 50 0.018
994
P CRV039 Cervicitis 49 0.018
995
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.018
996
HMP009 Haemophilus Influenzae 49 0.018
997
RTC005 Reticulosarcoma 49 0.018
998
HPT014 Hepatorenal Syndrome 49 0.018
999
BCT004 Bacteriuria 49 0.018
1000
DBT006 Diabetic Macular Edema 49 0.018
1001
c THR045 Thrombotic Thrombocytopenic Purpura, Congenital 49 0.018
1002
ANR004 Anuria 49 0.018
1003
NPH003 Nephrocalcinosis 49 0.018
1004
MNN009 Meningoencephalitis 49 0.018
1005
RNL077 Renal Fibrosis 49 0.018
1006
ASP007 Aspiration Pneumonia 49 0.018
1007
BLL003 Bell's Palsy 49 0.018
1008
P KRT007 Keratoconus 49 0.018
1009
EWN002 Ewing's Family of Tumors 49 0.018
1010
URT010 Ureteral Obstruction 49 0.018
1011
FRZ001 Frozen Shoulder 48 0.018
1012
FSC004 Fasciitis 48 0.018
1013
PLL012 Pollen Allergy 48 0.018
1014
DBT008 Diabetic Angiopathy 48 0.018
1015
P NNT009 Neonatal Diabetes Mellitus 48 0.018
1016
DSC009 Discoid Lupus Erythematosus 48 0.018
1017
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.018
1018
CHC001 Chickenpox 48 0.018
1019
ERY029 Erythermalgia, Primary 48 0.018
1020
AST006 Astigmatism 48 0.018
1021
P ENC008 Encephalocele 48 0.018
1022
VND001 Vein Disease 48 0.018
1023
PRP036 Peripheral T-Cell Lymphoma 48 0.018
1024
HRT015 Heritable Pulmonary Arterial Hypertension 48 0.018
1025
SNS003 Sensory Peripheral Neuropathy 48 0.018
1026
CVR006 Cavernous Hemangioma 48 0.018
1027
P CRN028 Corneal Ulcer 48 0.018
1028
DYS018 Dysostosis 48 0.018
1029
EPT010 Epithelial-Myoepithelial Carcinoma 48 0.018
1030
HYP025 Hyperphosphatemia 48 0.018
1031
c ACT020 Acute T Cell Leukemia 48 0.018
1032
PLC008 Placenta Disease 48 0.018
1033
SKN027 Skin Conditions 48 0.018
1034
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 48 0.018
1035
RGH009 Right Atrial Isomerism 48 0.018
1036
P MYS033 Miyoshi Muscular Dystrophy 1 48 0.018
1037
CRN017 Coronary Thrombosis 48 0.018
1038
P CMP008 Compartment Syndrome 48 0.018
1039
c ART120 Arthrogryposis, Distal, Type 3 47 0.018
1040
PRM003 Premature Ejaculation 47 0.018
1041
ESN020 Eosinophilic Granulomatosis with Polyangiitis 47 0.018
1042
SLV003 Salivary Gland Disease 47 0.018
1043
P CLS010 Cluster Headache 47 0.018
1044
DYS073 Dysphagia 47 0.018
1045
FCL022 Focal Dystonia 47 0.018
1046
CRB085 Cerebral Hemorrhage 47 0.018
1047
MCS004 Mucosal Melanoma 47 0.018
1048
NXS001 Naxos Disease 47 0.018
1049
P PSD003 Pseudohypoaldosteronism 47 0.018
1050
TRC062 Tricuspid Atresia 47 0.018
1051
CRN024 Corneal Disease 47 0.018
1052
MGR001 Migraine Without Aura 47 0.018
1053
DST006 Diastolic Heart Failure 47 0.018
1054
PRS129 Prostatic Hyperplasia, Benign 47 0.018
1055
AGG002 Aggressive Systemic Mastocytosis 47 0.018
1056
DNG001 Dengue Shock Syndrome 47 0.018
1057
ALP012 Alpha-Methylacyl-Coa Racemase Deficiency 46 0.018
1058
P ART084 Arteriovenous Fistula 46 0.018
1059
ESP002 Esophageal Varix 46 0.018
1060
CHR100 Chronic Ulcer of Skin 46 0.018
1061
P BLP003 Blepharospasm 46 0.018
1062
c MYS051 Myasthenic Syndrome, Congenital, 5 46 0.018
1063
INT038 Interdigitating Dendritic Cell Sarcoma 46 0.018
1064
SPN119 Spondylarthropathy 46 0.018
1065
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.018
1066
LKM006 Leukomalacia 46 0.018
1067
c EXS019 Exostoses, Multiple, Type I 46 0.018
1068
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.018
1069
CRB004 Cerebral Artery Occlusion 46 0.018
1070
NRR001 Neuroretinitis 46 0.018
1071
EXS001 Exostosis 46 0.018
1072
BCK006 Back Pain 46 0.018
1073
PRD004 Prediabetes Syndrome 46 0.018
1074
c ART144 Arthrogryposis, Distal, Type 1a 46 0.018
1075
OVR094 Ovarian Epithelial Cancer 46 0.018
1076
EPD070 Epidermoid Cysts 46 0.018
1077
c MTR002 Mitral Valve Insufficiency 46 0.018
1078
c CRN139 Cornelia De Lange Syndrome 1 46 0.018
1079
END072 Endotheliitis 46 0.018
1080
ENH001 Enhanced S-Cone Syndrome 46 0.018
1081
AMB002 Amblyopia 45 0.018
1082
BLD053 Blood Platelet Disease 45 0.018
1083
TND004 Tendinopathy 45 0.018
1084
ASP008 Aspiration Pneumonitis 45 0.018
1085
CNT025 Central Pontine Myelinolysis 45 0.018
1086
c ART061 Arthrogryposis, Distal, Type 2a 45 0.018
1087
MCR011 Microinvasive Gastric Cancer 45 0.018
1088
CRN031 Cranial Nerve Disease 45 0.018
1089
P HRN001 Horner's Syndrome 45 0.018
1090
c CNT015 Central Sleep Apnea 45 0.018
1091
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.018
1092
EBL001 Ebola Hemorrhagic Fever 45 0.018
1093
P HRD001 Hereditary Multiple Exostoses 45 0.018
1094
MCL027 Macular Dystrophy, Dominant Cystoid 45 0.018
1095
VST004 Vestibular Disease 45 0.018
1096
MTR003 Mitral Valve Stenosis 45 0.018
1097
RFR003 Refractive Error 45 0.018
1098
SXL003 Sexual Disorder 45 0.018
1099
LYM024 Lymphatic System Disease 45 0.018
1100
CRN055 Carney Triad 45 0.018
1101
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.018
1102
MSN001 Mesangial Proliferative Glomerulonephritis 45 0.018
1103
BRN080 Brain Ischemia 45 0.018
1104
P ATR010 Atrial Heart Septal Defect 45 0.018
1105
OCL069 Ocular Motor Apraxia 45 0.018
1106
TLR001 Tularemia 44 0.018
1107
ESN004 Eosinophilic Gastritis 44 0.018
1108
P PRP034 Purpura Fulminans 44 0.018
1109
PRN037 Prinzmetal's Variant Angina 44 0.018
1110
DCB001 Decubitus Ulcer 44 0.018
1111
P PYR039 Peyronie Disease 44 0.018
1112
SYN046