Search results for heart block

1205 hits were found for heart block

# Family MCID Name MIFTS Score
1
c PRG042 Progressive Familial Heart Block, Type Ia 57 8.808
2
c PRG043 Progressive Familial Heart Block, Type Ib 40 7.222
3
P HRT035 Heart Block, Congenital 45 7.123
4
c ATR087 Atrial Standstill 1 59 5.518
5
c PRG126 Progressive Familial Heart Block 46 4.578
6
c PRG101 Progressive Familial Heart Block, Type Ii 24 4.383
7
c FML250 Familial Progressive Cardiac Conduction Defect 33 3.440
8
SCN049 Second-Degree Atrioventricular Block 29 3.301
9
P ATR081 Atrial Standstill 34 1.997
10
SNR013 Sino-Auricular Heart Block 5 1.968
11
P HRT032 Heart Disease 80 0.814
12
CNG034 Congestive Heart Failure 74 0.529
13
P CRN300 Coronary Heart Disease 1 57 0.460
14
RGH001 Right Bundle Branch Block 44 0.375
15
ISC006 Ischemic Heart Disease 73 0.372
16
P MYC007 Myocardial Infarction 81 0.370
17
PNG002 Pain Agnosia 41 0.366
18
ATR057 Atrioventricular Block 52 0.311
19
ISC004 Ischemia 66 0.307
20
P CRN018 Coronary Artery Anomaly 69 0.278
21
c BLD140 Blood Group, I System 37 0.276
22
END072 Endotheliitis 46 0.262
23
ART140 Arteries, Anomalies of 51 0.260
24
SYS003 Systolic Heart Failure 44 0.255
25
P HYP055 Hypoplastic Left Heart Syndrome 63 0.251
26
c HYP543 Hypoplastic Left Heart Syndrome 1 38 0.241
27
P ATR011 Atrial Fibrillation 68 0.227
28
VSC007 Vascular Disease 71 0.223
29
P NRP001 Neuropathy 63 0.214
30
P ART021 Arteriosclerosis 62 0.211
31
AST005 Asthma 83 0.209
32
DST006 Diastolic Heart Failure 47 0.203
33
c ACT075 Acute Myocardial Infarction 64 0.199
34
AGN016 Aging 65 0.198
35
P BRS047 Breast Cancer 100 0.196
36
P ART022 Arthritis 77 0.194
37
ANX010 Anxiety 72 0.186
38
MNT002 Mental Depression 60 0.181
39
P KDN018 Kidney Disease 69 0.179
40
P DBT009 Diabetes Mellitus 72 0.177
41
P DLT002 Dilated Cardiomyopathy 76 0.173
42
P ART023 Arthropathy 68 0.169
43
P MYC008 Myocarditis 58 0.169
44
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.168
45
RHM028 Rheumatic Heart Disease 54 0.167
46
JNT002 Joint Disorders 60 0.162
47
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.162
48
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.160
49
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.156
50
P HPT021 Hepatitis 75 0.155
51
P PLM037 Pulmonary Hypertension 79 0.154
52
ANR040 Aneurysm 61 0.154
53
P NRV007 Nervous System Disease 75 0.153
54
LNG099 Lung Disease 67 0.153
55
RHM027 Rheumatic Disease 62 0.153
56
HRT012 Heart Valve Disease 45 0.153
57
RSP006 Respiratory System Disease 63 0.150
58
NRN002 Neuronitis 43 0.146
59
P SLP006 Sleep Apnea 65 0.144
60
RHM001 Rheumatic Fever 59 0.144
61
RHM035 Rheumatic Fever-Related Antigen 34 0.144
62
CNN005 Connective Tissue Disease 65 0.143
63
SYN036 Syncope 46 0.143
64
ENT004 Enthesopathy 38 0.143
65
THR024 Thrombosis 61 0.142
66
URN009 Urinary System Disease 58 0.142
67
P END033 Endocarditis 58 0.141
68
HYP266 Hypoxia 61 0.140
69
UNV002 Univentricular Heart 29 0.137
70
P CLL015 Collagen Disease 53 0.136
71
P HYP086 Hypothyroidism 62 0.135
72
BNF002 Bone Fracture 56 0.134
73
P HYP061 Hypertrophic Cardiomyopathy 65 0.134
74
P THY032 Thyroiditis 56 0.131
75
P LKM002 Leukemia 75 0.130
76
P LPS004 Lupus Erythematosus 69 0.129
77
P VNT002 Ventricular Septal Defect 59 0.129
78
HDC001 Headache 55 0.127
79
P SCK002 Sick Sinus Syndrome 53 0.127
80
OST012 Osteoarthritis 88 0.127
81
SLP005 Sleep Disorder 59 0.125
82
SPS003 Spastic Diplegia 55 0.124
83
ANG054 Angina Pectoris 53 0.124
84
P LNG032 Lung Cancer 99 0.123
85
PRS047 Prostatitis 59 0.123
86
P LNG028 Long Qt Syndrome 63 0.122
87
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.122
88
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.121
89
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.121
90
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.121
91
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.121
92
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.121
93
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.121
94
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.121
95
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.121
96
P MYP004 Myopathy 69 0.121
97
P RHM011 Rheumatoid Arthritis 91 0.120
98
c CHR089 Chronic Kidney Failure 72 0.120
99
P LYM118 Lymphoma 71 0.120
100
P TTR001 Tetralogy of Fallot 70 0.119
101
P CRD132 Cardiac Conduction Defect 53 0.119
102
P MYP006 Myopia 56 0.118
103
P CHR345 Chronic Pain 52 0.118
104
P PNC044 Pancreatitis 64 0.118
105
CRB039 Cerebrovascular Disease 68 0.117
106
THR099 Third-Degree Atrioventricular Block 37 0.117
107
P INF032 Infertility 59 0.117
108
CRD119 Cardiac Arrest 63 0.116
109
NRM005 Neuromuscular Disease 60 0.115
110
GLC008 Glucose Metabolism Disease 38 0.113
111
FRS012 First-Degree Atrioventricular Block 33 0.112
112
INF013 Inferior Myocardial Infarction 36 0.111
113
c PNS012 Paine Syndrome 52 0.110
114
DXT001 Dextrocardia 55 0.110
115
P ENC018 Encephalopathy 58 0.110
116
CRB009 Cerebritis 41 0.110
117
ATN005 Autonomic Dysfunction 51 0.109
118
BRR014 Barrett Esophagus 64 0.109
119
P MSC005 Muscular Dystrophy 66 0.108
120
CRD223 Cardiac Arrhythmia 52 0.108
121
P PRS040 Prostate Cancer 88 0.106
122
MLN008 Melanoma 72 0.106
123
c SYS001 Systemic Lupus Erythematosus 86 0.106
124
CRD003 Cardiac Sarcoidosis 40 0.106
125
P BRG001 Brugada Syndrome 61 0.104
126
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.104
127
c CNT035 Central Nervous System Disease 65 0.103
128
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.100
129
NRT004 Neuritis 55 0.099
130
c ART101 Aortic Valve Disease 2 65 0.099
131
INF034 Infective Endocarditis 56 0.099
132
ING001 Inguinal Hernia 59 0.097
133
P CRV039 Cervicitis 49 0.097
134
c ACT076 Acute Myocarditis 48 0.097
135
WLF001 Wolff-Parkinson-White Syndrome 57 0.097
136
TRN044 Transposition of the Great Arteries 49 0.096
137
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.096
138
P RSP003 Respiratory Failure 71 0.095
139
P PNM007 Pneumonia 70 0.095
140
PLM033 Pulmonary Embolism 62 0.095
141
c TRC078 Trichohepatoenteric Syndrome 2 34 0.095
142
SRC014 Sarcoma 68 0.094
143
P ANR048 Aniridia 1 68 0.094
144
P DYS021 Dysautonomia 47 0.094
145
PRP019 Peripheral Nervous System Disease 53 0.093
146
CRD137 Cardiogenic Shock 45 0.093
147
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 54 0.093
148
P INF038 Influenza 77 0.093
149
P ADN016 Adenocarcinoma 71 0.091
150
GST050 Gastrointestinal System Disease 66 0.091
151
PRP027 Peripheral Vascular Disease 71 0.091
152
ANR038 Anorexia Nervosa 1 21 0.091
153
BLD137 Blood Group--Ahonen 17 0.091
154
SKN016 Skin Disease 68 0.090
155
CMP010 Complex Regional Pain Syndrome 58 0.090
156
ANX004 Anoxia 49 0.090
157
KRN002 Kearns-Sayre Syndrome 59 0.090
158
END030 End Stage Renal Failure 59 0.089
159
SKN027 Skin Conditions 48 0.089
160
P LVR013 Liver Disease 76 0.088
161
BRS051 Breast Disease 67 0.088
162
END020 Endocardial Fibroelastosis 46 0.088
163
c HYP595 Hypertension, Essential 78 0.087
164
c PLM164 Pulmonary Hypertension, Primary, 1 67 0.087
165
P ATR010 Atrial Heart Septal Defect 45 0.086
166
CHG001 Chagas Disease 72 0.085
167
P AMY004 Amyloidosis 69 0.084
168
PNM008 Pneumothorax 57 0.084
169
PRP080 Peripheral Artery Disease 54 0.084
170
c HPT001 Hepatitis C 73 0.083
171
P RST002 Restrictive Cardiomyopathy 51 0.083
172
ATN002 Autonomic Nervous System Disease 51 0.083
173
THY030 Thyroid Gland Disease 51 0.083
174
ATM095 Autoimmune Disease 66 0.083
175
P CLR023 Colorectal Cancer 98 0.083
176
PLM010 Pulmonary Edema 57 0.082
177
c MTR002 Mitral Valve Insufficiency 46 0.082
178
MYL069 Myeloma, Multiple 86 0.082
179
MSC033 Muscle Disorders 53 0.082
180
HMP001 Hemopericardium 34 0.082
181
APN008 Apnea, Obstructive Sleep 67 0.082
182
MSC004 Muscle Tissue Disease 39 0.081
183
P RNG031 Ring Chromosome Y Syndrome 29 0.081
184
ATN004 Autonomic Neuropathy 46 0.081
185
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.081
186
c HPT073 Hepatitis C Virus 73 0.081
187
MLR004 Malaria 86 0.081
188
INS024 Insulin-Like Growth Factor I 83 0.081
189
P INT068 Intestinal Disease 65 0.080
190
P NNT042 Neonatal Lupus Erythematosus 38 0.080
191
P LFT003 Left Ventricular Noncompaction 52 0.079
192
PSY004 Psychotic Disorder 72 0.079
193
HYP005 Hypokalemia 53 0.079
194
HMN044 Human Immunodeficiency Virus Type 1 71 0.078
195
BRN071 Brain Injury 54 0.078
196
P PRC012 Pericardial Effusion 52 0.078
197
MDS022 Mediastinitis 44 0.078
198
OVR063 Overnutrition 53 0.078
199
PRP009 Peripartum Cardiomyopathy 53 0.077
200
ART016 Aortic Aneurysm 70 0.077
201
c PLM022 Pulmonary Valve Insufficiency 38 0.077
202
PRC013 Pericarditis 55 0.077
203
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 57 0.076
204
c SML038 Small Cell Cancer of the Lung 67 0.076
205
P EPL164 Epilepsy 70 0.076
206
P CTR002 Cataract 60 0.076
207
HYP066 Hyperglycemia 64 0.076
208
P HRP006 Herpes Simplex 70 0.075
209
GST053 Gastric Cancer 84 0.075
210
TRC062 Tricuspid Atresia 47 0.074
211
P MYT002 Myotonic Dystrophy 50 0.074
212
P HPT023 Hepatocellular Carcinoma 94 0.074
213
MYX004 Myxedema 44 0.074
214
LPD008 Lipid Metabolism Disorder 59 0.074
215
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.073
216
P HYP265 Hypotonia 40 0.073
217
CRN030 Coronary Stenosis 52 0.073
218
BCK006 Back Pain 46 0.073
219
STS002 Situs Inversus 48 0.073
220
HTR003 Heterotaxy 46 0.071
221
DBL004 Double Discordia 19 0.071
222
PST028 Post-Traumatic Stress Disorder 59 0.071
223
P PLY019 Polyneuropathy 58 0.071
224
c MLT151 Multiple Mitochondrial Dysfunctions Syndrome 5 36 0.070
225
FBR012 Fabry Disease 72 0.070
226
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 51 0.070
227
c ATM022 Autoimmune Myocarditis 40 0.070
228
PST053 Postherpetic Neuralgia 44 0.070
229
P ALZ034 Alzheimer Disease 95 0.070
230
IMM136 Immune System Disease 57 0.070
231
GNT019 Giant Cell Myocarditis 34 0.070
232
P MYC084 Mycobacterium Tuberculosis 1 69 0.070
233
BRC012 Brucellosis 71 0.070
234
P HYP076 Hyperthyroidism 56 0.070
235
EBS001 Ebstein Anomaly 52 0.069
236
c ACT071 Acute Kidney Failure 54 0.069
237
ART005 Arteriovenous Malformation 64 0.069
238
RTN023 Retinitis 52 0.069
239
P GLM045 Glioma 61 0.068
240
CRT016 Carotid Artery Disease 58 0.068
241
BRS090 Breast Reconstruction 41 0.068
242
MYC005 Myocardial Stunning 47 0.067
243
MTH009 Mouth Disease 64 0.067
244
TTH006 Tooth Disease 54 0.067
245
P PRD008 Periodontitis 67 0.067
246
PRT036 Peritonitis 67 0.067
247
P NRB001 Neuroblastoma 73 0.066
248
ART031 Aortic Coarctation 48 0.066
249
ALR002 Al-Raqad Syndrome 30 0.066
250
MBT001 Mobitz Type Ii Atrioventricular Block 15 0.066
251
IMM158 Immune Suppression 57 0.066
252
CNG134 Congenitally Corrected Transposition of the Great Arteries 28 0.066
253
P PHC003 Pheochromocytoma 72 0.066
254
CNT061 Conotruncal Heart Malformations 70 0.065
255
c HYP805 Hypercholesterolemia, Autosomal Dominant, 3 47 0.065
256
P TRC086 Trichohepatoenteric Syndrome 1 54 0.065
257
HYD012 Hydrops Fetalis 50 0.065
258
P OVR042 Ovarian Cancer 82 0.064
259
P HYP040 Hypospadias 60 0.064
260
DWN001 Down Syndrome 70 0.064
261
STR067 Stroke, Ischemic 84 0.063
262
CRD001 Cardiac Tamponade 45 0.063
263
ATR055 Atrial Septal Aneurysm 27 0.063
264
HMS001 Hemosiderosis 50 0.063
265
P ORT004 Orthostatic Intolerance 68 0.063
266
c MYT021 Myotonic Dystrophy 1 68 0.063
267
GNG013 Gingivitis 64 0.063
268
BRN106 Burns 57 0.063
269
HYD059 Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect 34 0.063
270
ACQ007 Acquired Immunodeficiency Syndrome 65 0.063
271
P THR014 Thrombocytopenia 65 0.063
272
HLT001 Holt-Oram Syndrome 61 0.062
273
c SCL052 Scleroderma, Familial Progressive 60 0.062
274
HRT008 Heart Conduction Disease 32 0.062
275
HYP056 Hypoglycemia 62 0.061
276
SPN051 Spondylitis 55 0.061
277
P ART084 Arteriovenous Fistula 46 0.061
278
PHR003 Pharyngitis 59 0.061
279
CYT008 Cytomegalovirus Infection 57 0.061
280
P DBT005 Diabetes Insipidus 54 0.061
281
c HPT003 Hepatitis a 63 0.061
282
c HPT016 Hepatitis B 68 0.061
283
RFL001 Reflex Sympathetic Dystrophy 51 0.061
284
MNN017 Mononeuropathy 42 0.061
285
ALG001 Algoneurodystrophy 39 0.061
286
c SPN225 Spondyloarthropathy 1 71 0.061
287
CRT028 Cor Triatriatum 25 0.061
288
SPN369 Spinal Disease 42 0.061
289
c FML001 Familial Atrial Fibrillation 55 0.060
290
PRN037 Prinzmetal's Variant Angina 44 0.060
291
P LRY019 Laryngitis 57 0.060
292
EPD070 Epidermoid Cysts 46 0.060
293
PRD007 Periodontal Disease 64 0.060
294
BLD163 Blood Group, Dombrock System 23 0.060
295
VRL011 Viral Infectious Disease 64 0.059
296
P PLY006 Polydactyly 57 0.059
297
MDD011 Mood Disorder 64 0.059
298
HYP060 Hyperinsulinism 56 0.059
299
SNG003 Single Ventricular Heart 23 0.059
300
c GRV008 Graves Disease 1 52 0.059
301
HRT011 Heart Septal Defect 44 0.059
302
BDY007 Body Mass Index Quantitative Trait Locus 1 23 0.059
303
P HMN010 Hemangioma 61 0.059
304
c SHR030 Short Qt Syndrome 42 0.059
305
CNS004 Constipation 57 0.059
306
LYM017 Lyme Disease 68 0.059
307
ART012 Aortitis 33 0.059
308
c ART115 Aortic Valve Disease 1 51 0.058
309
HTR014 Heterotaxy, Visceral, 1, X-Linked 39 0.058
310
CRB037 Cerebral Palsy 70 0.058
311
THR100 Thrombocytopenic Purpura, Autoimmune 57 0.058
312
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 54 0.058
313
CHL067 Cholecystitis 58 0.057
314
P PTS002 Ptosis 50 0.057
315
INF009 Inflammatory Spondylopathy 32 0.057
316
c PST001 Posterior Myocardial Infarction 28 0.057
317
CLT003 Colitis 63 0.057
318
VSC011 Vasculitis 66 0.057
319
P GLL020 Gallbladder Disease 64 0.057
320
SPN186 Spinal Cord Injury 67 0.056
321
P MSC003 Muscular Atrophy 55 0.056
322
NRR001 Neuroretinitis 46 0.056
323
TRG002 Trigeminal Neuralgia 60 0.056
324
PNC034 Pancreas Disease 59 0.056
325
P EMR001 Emery-Dreifuss Muscular Dystrophy 53 0.056
326
P SYS005 Systemic Scleroderma 67 0.056
327
SPS057 Spasticity 41 0.056
328
ANT005 Anteroseptal Myocardial Infarction 24 0.056
329
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.056
330
PTN001 Patent Foramen Ovale 58 0.056
331
P ATR001 Atrioventricular Septal Defect 56 0.056
332
SPR004 Supravalvular Aortic Stenosis 54 0.055
333
P MYS003 Myasthenia Gravis 73 0.055
334
P EXN002 Exanthem 62 0.055
335
c CRD099 Cardiomyopathy, Dilated, 1e 53 0.055
336
HPT082 Hepatic Adenomas, Familial 52 0.055
337
MTB004 Metabolic Acidosis 49 0.055
338
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 57 0.055
339
P ADL010 Adult Respiratory Distress Syndrome 67 0.055
340
SNT005 Sinoatrial Node Disease 31 0.055
341
DMN002 Dementia 68 0.055
342
GNT050 Genitourinary Tract Anomalies 41 0.055
343
VTM028 Vitamin E, Familial Isolated Deficiency of 52 0.055
344
P ENC004 Encephalitis 66 0.055
345
FRZ001 Frozen Shoulder 48 0.055
346
HDN002 Head Injury 48 0.054
347
ALC010 Alcoholic Cardiomyopathy 38 0.054
348
HRP004 Herpes Zoster 61 0.054
349
TRM010 Traumatic Brain Injury 54 0.054
350
SCK005 Sickle Cell Disease 54 0.054
351
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.054
352
P BCL006 B-Cell Lymphomas 70 0.054
353
CLN019 Colonic Disease 55 0.054
354
c SBC003 Subacute Bacterial Endocarditis 38 0.053
355
P ESP024 Esophagitis 64 0.053
356
P ANT001 Anterolateral Myocardial Infarction 24 0.053
357
GNR004 Generalized Anxiety Disorder 53 0.052
358
FNT004 Fainting 36 0.052
359
MRF001 Marfan Syndrome 75 0.052
360
P PTN014 Patent Ductus Arteriosus 1 45 0.052
361
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.052
362
P RHB003 Rhabdomyosarcoma 61 0.052
363
SPT001 Septal Myocardial Infarction 11 0.052
364
ALP046 Alport Syndrome, X-Linked 74 0.052
365
c MCL062 Mucolipidosis Ii Alpha/beta 58 0.052
366
PLC008 Placenta Disease 48 0.052
367
DBT010 Diabetic Neuropathy 60 0.051
368
PRS042 Prostate Disease 56 0.051
369
DYS073 Dysphagia 47 0.051
370
SQM006 Squamous Cell Carcinoma 74 0.051
371
P MYL006 Myeloid Leukemia 69 0.051
372
P PLM036 Pulmonary Fibrosis 68 0.051
373
P BLD051 Blood Coagulation Disease 38 0.051
374
MNG003 Mungan Syndrome 34 0.051
375
P RHN004 Rhinitis 62 0.051
376
P GRV001 Graves' Disease 62 0.051
377
BLD044 Bladder Disease 55 0.051
378
PRT055 Prieto X-Linked Mental Retardation Syndrome 30 0.051
379
PLY039 Polymorphic Reticulosis 22 0.051
380
ATH013 Atherosclerosis Susceptibility 59 0.051
381
P ANT006 Antiphospholipid Syndrome 59 0.051
382
MSC157 Muscular Dystrophy, Duchenne Type 74 0.051
383
RGH009 Right Atrial Isomerism 48 0.051
384
MSC152 Muscular Dystrophy, Becker Type 64 0.051
385
P MLT020 Multiple Sclerosis 85 0.050
386
MRB003 Morbid Obesity 61 0.050
387
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 27 0.050
388
P CRC039 Coarctation of Aorta 37 0.050
389
DXT002 Dextrocardia with Situs Inversus 32 0.050
390
CYS001 Cystic Fibrosis 85 0.050
391
P SCH015 Schizophrenia 71 0.050
392
PLM041 Pulmonary Valve Stenosis 48 0.050
393
c TRC022 Tricuspid Valve Insufficiency 36 0.050
394
NPH091 Nephrolithiasis, Calcium Oxalate 51 0.050
395
P CLC063 Celiac Disease 1 65 0.050
396
ALL006 Allergic Asthma 60 0.050
397
P GLM007 Glomerulonephritis 61 0.049
398
NPH009 Nephrolithiasis 57 0.049
399
P CHR071 Charcot-Marie-Tooth Disease 67 0.049
400
HRT006 Heart Aneurysm 18 0.049
401
c CNG006 Congenital Hypothyroidism 62 0.049
402
P STR035 Streptococcal Group a Invasive Disease 28 0.049
403
SCK003 Sickle Cell Anemia 73 0.049
404
P JRV004 Jervell and Lange-Nielsen Syndrome 1 54 0.049
405
CRC034 Carcinoma Showing Thymus-Like Differentiation 24 0.049
406
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.049
407
P PLM085 Pulmonary Hemosiderosis 48 0.049
408
PHC013 Phaeochromocytoma 44 0.049
409
BRN055 Bronchogenic Cyst 28 0.049
410
P CNJ013 Conjunctivitis 67 0.049
411
ART017 Aortic Disease 57 0.048
412
CHL123 Chlamydia 64 0.048
413
c CRD233 Cardiomyopathy, Dilated, 1b 51 0.048
414
PST048 Postural Orthostatic Tachycardia Syndrome 31 0.048
415
CRP001 Carpal Tunnel Syndrome 64 0.048
416
P FBR017 Fibrosarcoma 61 0.048
417
P LMY004 Leiomyosarcoma 59 0.048
418
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.048
419
CLF027 Cleft Palate, Isolated 61 0.047
420
MGR028 Migraine with or Without Aura 1 55 0.047
421
c ACT210 Acute Respiratory Distress Syndrome 63 0.047
422
P SPN046 Spinal Muscular Atrophy 63 0.047
423
CRT013 Carotid Stenosis 52 0.047
424
MLT131 Multifocal Atrial Tachycardia 19 0.047
425
BLR006 Biliary Tract Disease 55 0.047
426
P CLS010 Cluster Headache 47 0.047
427
P DMY001 Demyelinating Polyneuropathy 46 0.047
428
P MNN013 Meningitis 71 0.047
429
GST045 Gastroenteritis 65 0.047
430
STM007 Stomatitis 52 0.047
431
LVR012 Liver Cirrhosis 73 0.047
432
P ASP006 Aspergillosis 65 0.047
433
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 61 0.047
434
P PRX010 Paroxysmal Ventricular Fibrillation 28 0.047
435
P LPS002 Liposarcoma 61 0.046
436
BRN002 Bronchiolitis 59 0.046
437
TMT001 Timothy Syndrome 52 0.046
438
PST055 Postural Hypotension 40 0.046
439
CHR466 Chronic Thromboembolic Pulmonary Hypertension 43 0.046
440
LYM133 Lymphoma, Hodgkin, Classic 78 0.046
441
MXD005 Mixed Connective Tissue Disease 66 0.046
442
PRP030 Purpura 61 0.046
443
P PLY041 Polymyositis 57 0.046
444
PRS045 Prostatic Hypertrophy 51 0.046
445
PRT037 Pertussis 70 0.046
446
HMF006 Hemifacial Microsomia 58 0.046
447
MYT011 Myotonia 41 0.046
448
P OST002 Osteoporosis 75 0.046
449
c LNG044 Long Qt Syndrome 1 61 0.046
450
P TRC005 Tracheal Stenosis 39 0.046
451
WRN001 Werner Syndrome 70 0.046
452
P THL005 Thalassemia 65 0.046
453
GLC003 Glucose Intolerance 58 0.046
454
CRN017 Coronary Thrombosis 48 0.046
455
P RNL015 Renal Hypertension 46 0.046
456
RNL114 Renal Cell Carcinoma, Nonpapillary 68 0.045
457
P SRC025 Sarcoidosis 1 63 0.045
458
PLR022 Pleural Disease 54 0.045
459
c CRD065 Cardiomyopathy, Familial Hypertrophic, 2 42 0.045
460
P DYS154 Dystonia 61 0.045
461
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 57 0.045
462
URT001 Urethritis 44 0.045
463
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 37 0.045
464
NRV004 Nerve Compression Syndrome 37 0.045
465
PNC065 Pinched Nerve 15 0.045
466
PSR001 Psoriatic Arthritis 66 0.045
467
TTN003 Tetanus 65 0.045
468
QDR001 Quadriplegia 54 0.045
469
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 59 0.045
470
CLC006 Calcinosis 51 0.045
471
P TRN020 Turner Syndrome 69 0.045
472
DRM006 Dermatitis 67 0.045
473
P MYS005 Myositis 63 0.045
474
P SPN052 Spondyloarthropathy 61 0.045
475
P HMR012 Hemorrhagic Fever 60 0.045
476
NWB001 Newborn Respiratory Distress Syndrome 56 0.045
477
CHL004 Cholelithiasis 51 0.045
478
ADP007 Adie Pupil 41 0.045
479
P HYP120 Hypoaldosteronism 40 0.045
480
RSP007 Respiratory Distress Syndrome, Infant 28 0.045
481
DPH001 Diphtheria 63 0.044
482
INT075 Intracranial Hypertension 53 0.044
483
ATR048 Atrial Tachyarrhythmia with Short Pr Interval 34 0.044
484
P RTN024 Retinoblastoma 76 0.044
485
BRN028 Brain Cancer 72 0.044
486
ALL026 Allergic Hypersensitivity Disease 59 0.044
487
NRN004 Neuroendocrine Tumor 58 0.044
488
c ALZ056 Alzheimer Disease 3 41 0.044
489
P ANX007 Anauxetic Dysplasia 1 36 0.044
490
c ATR062 Atrial Septal Defect 1 32 0.044
491
HRT033 Heart-Hand Syndrome, Spanish Type 18 0.044
492
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 36 0.044
493
INT002 Intermittent Claudication 61 0.044
494
c CRD093 Cardiomyopathy, Dilated, 1a 58 0.044
495
ANR010 Aneurysm of Sinus of Valsalva 29 0.044
496
P INT030 Intracranial Aneurysm 58 0.043
497
P HMR005 Hemorrhoid 51 0.043
498
c BRG005 Brugada Syndrome 1 35 0.043
499
c SCK017 Sick Sinus Syndrome 1 23 0.043
500
c NNT025 Neonatal Systemic Lupus Erythematosus 16 0.043
501
c MYS011 Myasthenia Gravis Congenital 28 0.043
502
RSS026 Roussy-Levy Hereditary Areflexic Dystasia 53 0.043
503
P MYM013 Moyamoya Disease 1 50 0.043
504
P CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 24 0.043
505
HPR003 Heparin-Induced Thrombocytopenia 48 0.043
506
PLY001 Polycythemia Vera 75 0.043
507
P THR005 Thrombotic Thrombocytopenic Purpura 63 0.043
508
DFF003 Diffuse Scleroderma 44 0.043
509
NRL016 Neural Tube Defects 79 0.043
510
BRN024 Bronchitis 67 0.043
511
TKY002 Takayasu Arteritis 66 0.043
512
FTT001 Fatty Liver Disease 62 0.043
513
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 55 0.043
514
PLM068 Pulmonary Vein Stenosis 43 0.043
515
LVC002 Levocardia 20 0.043
516
c CNG385 Congenital Heart Defects, Multiple Types, 3 16 0.043
517
SNS001 Sensorineural Hearing Loss 59 0.042
518
P SJG008 Sjogren Syndrome 58 0.042
519
ANK001 Ankylosis 56 0.042
520
STM006 Stomach Disease 52 0.042
521
THY028 Thyroid Cancer 72 0.042
522
NRV006 Nervous System Cancer 61 0.042
523
c CHR283 Chronic Inflammatory Demyelinating Polyneuropathy 51 0.042
524
P PRT013 Portal Hypertension 59 0.041
525
PRP016 Paraplegia 53 0.041
526
GNG011 Gingival Disease 50 0.041
527
MYF002 Myofascial Pain Syndrome 44 0.041
528
c BRG007 Brugada Syndrome 5 33 0.041
529
P DRR001 Diarrhea 60 0.041
530
CLF001 Cleft Lip 54 0.041
531
c LNG048 Long Qt Syndrome 3 46 0.041
532
BRN012 Bronchiolitis Obliterans 60 0.041
533
P SZR006 Seizure Disorder 55 0.041
534
c LNG057 Long Qt Syndrome 13 39 0.041
535
P NNN008 Noonan Syndrome 1 77 0.041
536
c ADM005 Adams-Oliver Syndrome 1 38 0.041
537
APP008 Appendicitis 64 0.041
538
ADN018 Adenoma 63 0.041
539
OVR077 Overuse Syndrome 23 0.041
540
CML001 Cumulative Trauma Disorders 23 0.041
541
RPT005 Repetitive Motion Disorders 20 0.041
542
RPT006 Repetitive Stress Injuries 14 0.041
543
ACT119 Acute Promyelocytic Leukemia 64 0.040
544
LMY002 Leiomyoma 58 0.040
545
ERY008 Erythromelalgia 53 0.040
546
P INF037 Inflammatory Bowel Disease 52 0.040
547
P CMP008 Compartment Syndrome 48 0.040
548
c FML191 Familial Long Qt Syndrome 43 0.040
549
ATR089 Atrioventricular Dissociation 17 0.040
550
P PLM034 Pulmonary Emphysema 59 0.040
551
P HYP083 Hypopituitarism 59 0.040
552
P HYD006 Hydrocephalus 68 0.040
553
GST023 Gastric Ulcer 57 0.040
554
P LMB006 Limb-Girdle Muscular Dystrophy 55 0.040
555
P CTN003 Cutaneous Lupus Erythematosus 53 0.040
556
ACH005 Achalasia 52 0.040
557
P KLP003 Klippel-Feil Syndrome 46 0.040
558
BRN080 Brain Ischemia 45 0.040
559
P PLV020 Pelvic Organ Prolapse 63 0.040
560
PLS006 Plasmodium Vivax Malaria 56 0.040
561
P UTR058 Uterine Anomalies 55 0.040
562
P TCL004 T-Cell Leukemia 50 0.040
563
SDD001 Sudden Infant Death Syndrome 61 0.040
564
HST009 Histiocytoma 51 0.040
565
RNL077 Renal Fibrosis 49 0.040
566
c BRG006 Brugada Syndrome 2 25 0.040
567
c MYC058 Myocardial Infarction 2 25 0.040
568
CNN003 Conn's Syndrome 70 0.039
569
P DBT085 Diabetes Mellitus, Insulin-Dependent 69 0.039
570
P PSR002 Psoriasis 65 0.039
571
RFS006 Refsum Disease, Classic 63 0.039
572
P ALC004 Alcohol Abuse 63 0.039
573
P HMR003 Hemorrhagic Disease 61 0.039
574
BRN038 Bronchial Disease 58 0.039
575
RLP001 Relapsing Polychondritis 55 0.039
576
c BLM008 Bulimia Nervosa 2 53 0.039
577
MVM001 Movement Disease 40 0.039
578
c PRC016 Pre-Eclampsia 65 0.039
579
P GLY013 Glycogen Storage Disease 61 0.039
580
CHR103 Charge Syndrome 59 0.039
581
ANG020 Angiosarcoma 57 0.039
582
ART008 Arteriosclerosis Obliterans 45 0.039
583
DXR001 Doxorubicin Induced Cardiomyopathy 40 0.039
584
LYM143 Lymphoma, Non-Hodgkin, Familial 71 0.038
585
P MCK013 Meckel Syndrome, Type 1 62 0.038
586
P CNT004 Centronuclear Myopathy 54 0.038
587
GTR002 Goiter 53 0.038
588
c LNG051 Long Qt Syndrome 6 42 0.038
589
MCR103 Microtia 39 0.038
590
INT084 Intrinsic Cardiomyopathy 29 0.038
591
P SCL057 Scoliosis, Isolated 1 28 0.038
592
WLD005 Wild Type Attr Amyloidosis 24 0.038
593
P MDL005 Medulloblastoma 76 0.038
594
RTN018 Retinal Disease 56 0.038
595
P DNG005 Dengue Virus 56 0.038
596
PST021 Postpartum Depression 54 0.038
597
MDN002 Median Neuropathy 32 0.038
598
VRC005 Varicose Veins 64 0.038
599
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.038
600
AMY087 Amyloidosis, Hereditary, Transthyretin-Related 57 0.038
601
P ECL001 Eclampsia 57 0.038
602
P RNV001 Renovascular Hypertension 48 0.038
603
PCT003 Pectus Excavatum 44 0.038
604
BNM029 Bone Mineral Density Quantitative Trait Locus 15 39 0.038
605
BNM022 Bone Mineral Density Quantitative Trait Locus 8 32 0.038
606
HSH003 Hashimoto Thyroiditis 67 0.038
607
PRM042 Primary Effusion Lymphoma 61 0.038
608
TMP001 Temporal Lobe Epilepsy 54 0.038
609
c CRD232 Cardiomyopathy, Familial Hypertrophic, 6 31 0.038
610
PHN003 Phenylketonuria 73 0.037
611
P DRM010 Dermatomyositis 65 0.037
612
c GLY008 Glycogen Storage Disease Ii 64 0.037
613
P HMP007 Hemophilia 61 0.037
614
DSS009 Disseminated Intravascular Coagulation 56 0.037
615
RSP002 Respiratory Syncytial Virus Infectious Disease 53 0.037
616
CHP002 Chops Syndrome 40 0.037
617
SCR015 Scarlet Fever 40 0.037
618
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 35 0.037
619
c LKM071 Leukemia, Chronic Lymphocytic 75 0.037
620
P AST007 Astrocytoma 66 0.037
621
P SNS014 Sinusitis 62 0.037
622
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.036
623
P PLY014 Polycystic Kidney Disease 60 0.036
624
PRN038 Prune Belly Syndrome 55 0.036
625
CRB085 Cerebral Hemorrhage 47 0.036
626
TRC021 Tricuspid Valve Stenosis 40 0.036
627
P PLM040 Pulmonary Valve Disease 38 0.036
628
PLM001 Pulmonary Tuberculosis 72 0.036
629
P LYM025 Lymphedema 63 0.036
630
MCS002 Mucositis 61 0.036
631
DBT062 Diabetic Foot Ulcers 59 0.036
632
ABL002 Ablepharon-Macrostomia Syndrome 55 0.036
633
APP015 Apparent Mineralocorticoid Excess 54 0.036
634
EWN002 Ewing's Family of Tumors 49 0.036
635
c LNG053 Long Qt Syndrome 9 40 0.036
636
P MNN007 Meningocele 38 0.036
637
MNT310 Mental Retardation, X-Linked, Syndromic, Snyder-Robinson Type 32 0.036
638
c MLG036 Malignant Spiradenoma 31 0.036
639
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 70 0.036
640
P CRN037 Craniosynostosis 68 0.036
641
P MCR115 Microvascular Complications of Diabetes 5 66 0.036
642
INT066 Interstitial Lung Disease 63 0.036
643
c THR092 Thrombophilia Due to Thrombin Defect 61 0.036
644
UND005 Undifferentiated Pleomorphic Sarcoma 59 0.036
645
P CYS018 Cystitis 57 0.036
646
BLR001 Biliary Atresia 56 0.036
647
GST037 Gastroparesis 56 0.036
648
P MTC133 Mitochondrial Myopathy 53 0.036
649
FBR032 Fibromuscular Dysplasia 53 0.036
650
c LNG047 Long Qt Syndrome 2 49 0.036
651
ISC002 Ischemic Optic Neuropathy 48 0.036
652
P MTH007 Methemoglobinemia 46 0.036
653
c MSC050 Muscular Dystrophy, Congenital, 1b 45 0.036
654
LYM024 Lymphatic System Disease 45 0.036
655
MYT026 Myotonia Atrophica 21 0.036
656
P PRK057 Parkinson Disease, Late-Onset 78 0.035
657
TRN015 Transient Cerebral Ischemia 58 0.035
658
P ANG015 Angioedema 57 0.035
659
c MCR113 Microvascular Complications of Diabetes 3 55 0.035
660
ESP020 Esophageal Atresia 54 0.035
661
ANR004 Anuria 49 0.035
662
c OPT051 Opitz Gbbb Syndrome, Type I 47 0.035
663
CRD054 Cardiac Arrhythmia, Ankyrin-B-Related 24 0.035
664
HSB001 His Bundle Tachycardia 23 0.035
665
STR029 Sternal Cleft 21 0.035
666
ATR024 Atrial Fibrillation and Stroke 18 0.035
667
P GRF003 Graft-Versus-Host Disease 72 0.035
668
DFF005 Diffuse Large B-Cell Lymphoma 64 0.035
669
P LPR021 Leprosy 3 59 0.035
670
P SML001 Small Cell Carcinoma 58 0.035
671
PRP007 Priapism 49 0.035
672
DBT008 Diabetic Angiopathy 48 0.035
673
c CHR095 Chronic Progressive External Ophthalmoplegia 44 0.035
674
TRC026 Tracheal Disease 35 0.035
675
CCL002 Cecal Disease 34 0.035
676
c LPR012 Leopard Syndrome 1 33 0.035
677
c GLY009 Glycogen Storage Disease Xv 26 0.035
678
ULC005 Ulcer of Lower Limbs 23 0.035
679
PST017 Posterolateral Myocardial Infarction 20 0.035
680
ERL052 Early Repolarization Associated with Ventricular Fibrillation 16 0.035
681
PHC005 Phacomatosis Pigmentokeratotica 14 0.035
682
ALL003 Allergic Rhinitis 68 0.035
683
P LTR001 Lateral Sclerosis 58 0.035
684
TND005 Tendinitis 42 0.035
685
c LKM004 Leukemia, B-Cell, Chronic 37 0.035
686
URT037 Urethral Stricture 35 0.035
687
FTD001 Foot Drop 35 0.035
688
INT053 Intracranial Vasospasm 25 0.035
689
P FCS012 Facioscapulohumeral Muscular Dystrophy 1 56 0.034
690
P HML001 Hemolytic-Uremic Syndrome 50 0.034
691
PYL006 Pyloric Stenosis 47 0.034
692
c WLM011 Wilms Tumor 6 44 0.034
693
OST062 Osteoarthritis with Mild Chondrodysplasia 43 0.034
694
c LNG050 Long Qt Syndrome 5 43 0.034
695
MTC004 Mitochondrial Encephalomyopathy 42 0.034
696
P ENC011 Encephalomyopathy 40 0.034
697
c LNG056 Long Qt Syndrome 12 36 0.034
698
GND003 Gonadal Disease 32 0.034
699
CRD237 Cardiomyopathy, Dilated, 1aa, with or Without Left Ventricular Noncompaction 22 0.034
700
P ATX030 Ataxia-Telangiectasia 80 0.034
701
DNG002 Dengue Hemorrhagic Fever 66 0.034
702
HTC003 Hutchinson-Gilford Progeria Syndrome 62 0.034
703
c ACT027 Acute Pancreatitis 61 0.034
704
MRK001 Merkel Cell Carcinoma 59 0.034
705
P NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 57 0.034
706
P THY054 Thyrotoxic Periodic Paralysis 54 0.034
707
PRN011 Pernicious Anemia 50 0.034
708
c FML294 Familial Short Qt Syndrome 34 0.034
709
HYP226 Hyporeninemic Hypoaldosteronism 25 0.034
710
MXD001 Mixed Cerebral Palsy 20 0.034
711
DGT004 Digitalis Poisoning 12 0.034
712
SMT004 Smith-Lemli-Opitz Syndrome 70 0.034
713
P NRC002 Narcolepsy 64 0.034
714
P BPL003 Bipolar Disorder 61 0.034
715
PLS011 Plasmacytoma 60 0.034
716
P VNS003 Venous Insufficiency 53 0.034
717
c MLG074 Malignant Mesenchymoma 51 0.034
718
NRL018 Neural Tube Defects, Folate-Sensitive 44 0.034
719
TRN012 Transient Global Amnesia 40 0.034
720
FXF002 Fox-Fordyce Disease 40 0.034
721
ALC007 Alcohol Dependence 65 0.033
722
BRG013 Buerger Disease 62 0.033
723
P MLG056 Malignant Hyperthermia 60 0.033
724
VGN023 Vaginitis 59 0.033
725
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.033
726
LYM019 Lymphosarcoma 58 0.033
727
P CHN012 Chondrosarcoma 56 0.033
728
P OBS001 Obstructive Jaundice 53 0.033
729
P OVR046 Ovarian Cyst 52 0.033
730
FCL012 Facial Paralysis 50 0.033
731
P HMC002 Homocystinuria 50 0.033
732
RYN001 Raynaud Disease 48 0.033
733
P HRD009 Hereditary Wilms' Tumor 46 0.033
734
P RTN014 Retinal Artery Occlusion 45 0.033
735
CRN041 Carnitine-Acylcarnitine Translocase Deficiency 44 0.033
736
CRB086 Cerebral Aneurysms 42 0.033
737
ANG066 Angel-Shaped Phalangoepiphyseal Dysplasia 33 0.033
738
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 29 0.033
739
c LNG045 Long Qt Syndrome 10 21 0.033
740
c ATR064 Atrioventricular Septal Defect 3 17 0.033
741
P TBR001 Tuberous Sclerosis 69 0.032
742
P ATT013 Attention Deficit-Hyperactivity Disorder 67 0.032
743
CNT097 Central Hypoventilation Syndrome, Congenital 65 0.032
744
PMS001 Poems Syndrome 64 0.032
745
GST033 Gestational Diabetes 62 0.032
746
VSC002 Vascular Dementia 58 0.032
747
P ALP008 Alopecia 56 0.032
748
HYP080 Hypogonadism 54 0.032
749
P ADM011 Adams-Oliver Syndrome 52 0.032
750
CLB010 Coloboma of Macula 52 0.032
751
ARR018 Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 42 0.032
752
ARR045 Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 38 0.032
753
GLS018 Glass Syndrome 38 0.032
754
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 36 0.032
755
P ART106 Arterial Calcification, Generalized, of Infancy, 1 36 0.032
756
c CRD155 Cardiomyopathy, Dilated, 1kk 23 0.032
757
CRT061 Cor Triatriatum Dexter 18 0.032
758
c PSD047 Pseudo-Turner Syndrome 15 0.032
759
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.032
760
CHL065 Cholangiocarcinoma 70 0.032
761
GST092 Gastroesophageal Reflux 64 0.032
762
ARC002 Arachnoiditis 45 0.032
763
PRG039 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 40 0.032
764
P BRN120 Bronchus Cancer 39 0.032
765
ACL001 Acalculous Cholecystitis 39 0.032
766
PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 36 0.032
767
c LKM056 Leukemia, Chronic Lymphocytic 2 35 0.032
768
PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 35 0.032
769
TCK002 Tick Paralysis 22 0.032
770
LYS023 Lysis by Alloreactive Natural Killer Cells 11 0.032
771
c MNN043 Meningioma, Familial 69 0.032
772
P TMP003 Temporal Arteritis 67 0.032
773
INS001 Insulinoma 66 0.032
774
ADR054 Adrenocortical Carcinoma, Hereditary 63 0.032
775
c ATM011 Autoimmune Hepatitis 63 0.032
776
P EHL001 Ehlers-Danlos Syndrome 61 0.032
777
LNG039 Lung Squamous Cell Carcinoma 60 0.032
778
SLC006 Silicosis 57 0.032
779
P CTN015 Cutaneous T Cell Lymphoma 56 0.032
780
LST001 Listeriosis 55 0.032
781
ASP003 Aseptic Meningitis 54 0.032
782
CLL003 Cellulitis 53 0.032
783
P CRN108 Cranioectodermal Dysplasia 1 53 0.032
784
P RNL007 Renal Tubular Acidosis 51 0.032
785
SLV003 Salivary Gland Disease 47 0.032
786
NSP002 Nasopharyngitis 46 0.032
787
CRV043 Cervical Dystonia 45 0.032
788
TRC023 Trichinosis 45 0.032
789
RTR001 Retrograde Amnesia 40 0.032
790
MYC033 Myoclonus 40 0.032
791
c NNN012 Noonan Syndrome 5 39 0.032
792
GLS004 Glossopharyngeal Neuralgia 34 0.032
793
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 33 0.032
794
c FML272 Familial Sick Sinus Syndrome 26 0.032
795
PRM183 Primary Aldosteronism, Seizures, and Neurologic Abnormalities 23 0.032
796
c CRD061 Cardiomyopathy, Familial Hypertrophic, 13 21 0.032
797
P AST055 Asthma-Related Traits 1 18 0.032
798
MYL009 Myelodysplastic Syndrome 75 0.031
799
LPT001 Leptospirosis 64 0.031
800
HYP020 Hyperprolactinemia 64 0.031
801
RCK004 Rickets 63 0.031
802
BRN056 Bronchopulmonary Dysplasia 61 0.031
803
PLC005 Placental Insufficiency 59 0.031
804
HMR039 Hemorrhage, Intracerebral 57 0.031
805
PRR016 Pierre Robin Syndrome 57 0.031
806
P PYL005 Pyelonephritis 56 0.031
807
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 47 0.031
808
PST011 Pustulosis of Palm and Sole 47 0.031
809
PLY012 Polyhydramnios 47 0.031
810
DNG001 Dengue Shock Syndrome 47 0.031
811
BSL008 Basal Ganglia Disease 44 0.031
812
c MCR130 Microvascular Complications of Diabetes 6 42 0.031
813
OLV002 Oliver Syndrome 41 0.031
814
HYL004 Hyaline Fibromatosis Syndrome 40 0.031
815
VSC008 Vascular Hemostatic Disease 36 0.031
816
c MCR120 Microvascular Complications of Diabetes 7 34 0.031
817
c MCR133 Microvascular Complications of Diabetes 4 32 0.031
818
FCT002 Factor Xi Deficiency 64 0.030
819
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.030
820
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 63 0.030
821
P INT143 Interstitial Cystitis 63 0.030
822
TNS005 Tonsillitis 61 0.030
823
HPT022 Hepatoblastoma 55 0.030
824
CHL028 Childhood Type Dermatomyositis 55 0.030
825
P PRM006 Primary Biliary Cirrhosis 55 0.030
826
CND002 Conduct Disorder 54 0.030
827
SPN041 Spinal Cord Disease 54 0.030
828
HMG002 Hemoglobinuria 52 0.030
829
CCN001 Cocaine Dependence 52 0.030
830
SCH012 Schizoaffective Disorder 51 0.030
831
NNN026 Noonan Syndrome with Multiple Lentigines 49 0.030
832
CVR006 Cavernous Hemangioma 48 0.030
833
SPS007 Spastic Cerebral Palsy 46 0.030
834
TRT001 Teratocarcinoma 41 0.030
835
INT011 Interstitial Emphysema 40 0.030
836
GGN002 Gigantism 36 0.030
837
c BLR024 Biliary Cirrhosis, Primary, 1 35 0.030
838
c SRC023 Sarcoidosis 2 30 0.030
839
UND007 Undifferentiated Connective Tissue Disease 28 0.030
840
c SNG011 Singleton-Merten Syndrome 1 23 0.030
841
MCR311 Microcephaly, Cerebellar Hypoplasia, and Cardiac Conduction Defect Syndrome 20 0.030
842
CYN003 Cyanide Poisoning 19 0.030
843
ARR041 Arrhythmogenic Right Ventricular Dysplasia, Familial, 13 18 0.030
844
EXT058 Extrasystoles, Multiform Ventricular, with Short Stature, Hyperpigmentation and Microcephaly 18 0.030
845
MSC030 Muscular Fibrosis Multifocal Obstructed Vessels 14 0.030
846
c INF055 Infectious Myocarditis 13 0.030
847
PLM134 Pulmonary Fibrosis, Idiopathic 73 0.029
848
BRT054 Brittle Bone Disorder 67 0.029
849
P PRD006 Prader-Willi Syndrome 66 0.029
850
PRP001 Propionic Acidemia 63 0.029
851
SRC027 Sarcoma, Synovial 58 0.029
852
BDD001 Budd-Chiari Syndrome 58 0.029
853
CYS005 Cysticercosis 57 0.029
854
NNL002 Nonalcoholic Steatohepatitis 56 0.029
855
P SCL018 Scoliosis 56 0.029
856
GST009 Gastroschisis 55 0.029
857
PNM001 Pneumocystosis 55 0.029
858
P SYP003 Syphilis 55 0.029
859
PRT038 Protein-Energy Malnutrition 52 0.029
860
c PST041 Posterior Urethral Valves 51 0.029
861
HPT014 Hepatorenal Syndrome 49 0.029
862
c THR045 Thrombotic Thrombocytopenic Purpura, Congenital 49 0.029
863
SKL017 Skeletal Dysplasias 48 0.029
864
GYN001 Gynecomastia 47 0.029
865
c HYP795 Hypothyroidism, Congenital, Nongoitrous, 4 45 0.029
866
CRB008 Cerebral Atherosclerosis 42 0.029
867
HYP064 Hypogonadotropism 38 0.029
868
CYT004 Cytomegalic Inclusion Disease 35 0.029
869
THY001 Thyroid Crisis 30 0.029
870
PRM008 Parametritis 29 0.029
871
FBR028 Fibrosing Mediastinitis 28 0.029
872
INF021 Infant Gynecomastia 25 0.029
873
MYX011 Myxozoa 19 0.029
874
c BRG003 Brugada Syndrome 3 17 0.029
875
c BRG004 Brugada Syndrome 4 16 0.029
876
c ATR093 Atrial Heart Septal Defect 7 12 0.029
877
c LKM063 Leukemia, Chronic Myeloid 80 0.029
878
ULC004 Ulcerative Colitis 80 0.029
879
NRF026 Neurofibromatosis, Type Iv, of Riccardi 72 0.029
880
GLB015 Glioblastoma Multiforme 68 0.029
881
c ADL017 Adult T-Cell Leukemia 63 0.029
882
P SBS003 Substance Abuse 57 0.029
883
EPD016 Epidermolysis Bullosa 57 0.029
884
NRM004 Neuroma 51 0.029
885
P HML033 Hemolytic Uremic Syndrome, Atypical 1 49 0.029
886
PLY020 Polyradiculoneuropathy 48 0.029
887
PRS129 Prostatic Hyperplasia, Benign 47 0.029
888
CRB004 Cerebral Artery Occlusion 46 0.029
889
P AXN001 Axonal Neuropathy 38 0.029
890
MNN028 Mononeuropathy of the Median Nerve, Mild 35 0.029
891
c CTR119 Cataract 32, Multiple Types 32 0.029
892
P UVT001 Uveitis 61 0.028
893
VNW001 Von Willebrand's Disease 61 0.028
894
DMY004 Demyelinating Disease 58 0.028
895
BRN004 Brain Edema 57 0.028
896
ECT006 Ectodermal Dysplasia 57 0.028
897
c HPT007 Hepatitis E 57 0.028
898
P HYP726 Hypercalcemia, Infantile, 1 57 0.028
899
EXF001 Exfoliation Syndrome 55 0.028
900
EHL034 Ehlers-Danlos Syndrome, Hypermobility Type 51 0.028
901
EXP004 Exophthalmos 50 0.028
902
PNC001 Pancytopenia 50 0.028
903
c WLM018 Wilms Tumor 5 49 0.028
904
P LSS002 Lissencephaly 49 0.028
905
SMN007 Seminoma 49 0.028
906
SPN119 Spondylarthropathy 46 0.028
907
MYC013 Mycobacterium Abscessus 45 0.028
908
MNN021 Meningococcemia 43 0.028
909
c SBC007 Subacute Thyroiditis 43 0.028
910
c HYP794 Hyperoxaluria, Primary, Type I 41 0.028
911
ADN002 Adenoiditis 40 0.028
912
c CNT028 Central Retinal Artery Occlusion 40 0.028
913
P BCT020 Bacteremia 2 34 0.028
914
c CRD148 Cardiomyopathy, Familial Hypertrophic, 16 19 0.028
915
CHR628 Charcot-Marie-Tooth Disease, Guadalajara Neuronal Type 13 0.028
916
CHR152 Charcot-Marie-Tooth Disease with Ptosis and Parkinsonism 13 0.028
917
GST019 Gastrointestinal Stromal Tumor 74 0.027
918
c HMP029 Hemophilia a 69 0.027
919
NRF007 Neurofibroma 65 0.027
920
P MCP040 Mucopolysaccharidosis-Plus Syndrome 61 0.027
921
SCH078 Schimmelpenning-Feuerstein-Mims Syndrome 60 0.027
922
MSC165 Muscular Dystrophy, Congenital, Lmna-Related 59 0.027
923
P OVR049 Ovarian Disease 58 0.027
924
MTC027 Mitochondrial Trifunctional Protein Deficiency 55 0.027
925
P CHL066 Cholangitis 52 0.027
926
P PRC019 Precocious Puberty 52 0.027
927
TRS021 Triosephosphate Isomerase Deficiency 51 0.027
928
GSG001 Gas Gangrene 51 0.027
929
FCT001 Factor Viii Deficiency 50 0.027
930
CLF004 Cleft Lip/palate 49 0.027
931
NPH003 Nephrocalcinosis 49 0.027
932
CRB045 Cerebellar Hypoplasia 48 0.027
933
DWR001 Dwarfism 48 0.027
934
SPN035 Spindle Cell Sarcoma 46 0.027
935
P HYP009 Hypertrophic Pyloric Stenosis 45 0.027
936
INT071 Intestinal Perforation 44 0.027
937
c MYP072 Myopathy, Myofibrillar, 1 44 0.027
938
ACT058 Active Peptic Ulcer Disease 43 0.027
939
P PRC031 Preeclampsia/eclampsia 1 41 0.027
940
CHR073 Choreatic Disease 40 0.027
941
CHR178 Chromosomal Triplication 35 0.027
942
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 33 0.027
943
HMF010 Hemifacial Microsomia with Radial Defects 31 0.027
944
SLN001 Silent Myocardial Infarction 28 0.027
945
FDL001 Fiedler's Myocarditis 24 0.027
946
c BRG009 Brugada Syndrome 7 18 0.027
947
c BRG012 Brugada Syndrome 9 17 0.027
948
c BRG008 Brugada Syndrome 6 17 0.027
949
c BRG010 Brugada Syndrome 8 16 0.027
950
c SCK022 Sick Sinus Syndrome 3 13 0.027
951
KPS004 Kaposi Sarcoma 73 0.025
952
P DMN001 Diamond-Blackfan Anemia 70 0.025
953
P DRM053 Dermatitis, Atopic 68 0.025
954
LYM007 Lymphangioleiomyomatosis 68 0.025
955
P PRS038 Personality Disorder 65 0.025
956
INC002 Inclusion Body Myositis 64 0.025
957
HMR004 Hemorrhagic Fever with Renal Syndrome 63 0.025
958
YLL002 Yellow Fever 63 0.025
959
CHL068 Cholestasis 60 0.025
960
c OST080 Osteogenesis Imperfecta, Type Ii 59 0.025
961
c BCT007 Bacterial Meningitis 59 0.025
962
ICH054 Ichthyosis, X-Linked 59 0.025
963
STS003 Sitosterolemia 58 0.025
964
PLM012 Pulmonary Sarcoidosis 58 0.025
965
SPH001 Sapho Syndrome 54 0.025
966
c PRM012 Primary Polycythemia 53 0.025
967
PST095 Post-Thrombotic Syndrome 52 0.025
968
c ACT134 Acute Liver Failure 52 0.025
969
MYL001 Myelitis 52 0.025
970
CHL061 Childhood Leukemia 50 0.025
971
ANS023 Anus, Imperforate 50 0.025
972
LRN003 Learning Disability 49 0.025
973
PTT037 Pituitary Tumors 49 0.025
974
GLC009 Glucosephosphate Dehydrogenase Deficiency 48 0.025
975
MYC012 Mycetoma 46 0.025
976
SWN001 Swine Influenza 46 0.025
977
P TRT019 Torticollis 45 0.025
978
CRT009 Critical Illness Polyneuropathy 44 0.025
979
RTR011 Retroperitoneal Fibrosis 43 0.025
980
c ADL027 Adult Dermatomyositis 41 0.025
981
c SMP007 Simpson-Golabi-Behmel Syndrome, Type 1 40 0.025
982
END014 Endemic Typhus 38 0.025
983
BLT003 Blue Toe Syndrome 38 0.025
984
c SBC035 Subacute Cutaneous Lupus Erythematosus 37 0.025
985
SXD001 Sex Differentiation Disease 37 0.025
986
FML304 Familial Isolated Dilated Cardiomyopathy 36 0.025
987
SPN331 Spondyloocular Syndrome 34 0.025
988
c INF145 Infantile Liver Failure Syndrome 1 33 0.025
989
ALP072 Alpha-Fetoprotein Deficiency 32 0.025
990
NRG005 Neurogenic Hypertension 29 0.025
991
c LNG098 Long Qt Syndrome 14 26 0.025
992
ATR088 Atrial Septal Defect 7 with or Without Atrioventricular Conduction Defects 24 0.025
993
CRD006 Cardiovascular Syphilis 24 0.025
994
XP2002 Xp22.13p22.2 Duplication Syndrome 23 0.025
995
c SCK014 Sick Sinus Syndrome 2 22 0.025
996
XQ1001 Xq12-Q13.3 Duplication Syndrome 20 0.025
997
PHC017 Pheochromocytoma--Islet Cell Tumor Syndrome 20 0.025
998
BLD138 Blood Group--Diego System 18 0.025
999
MNT001 Mantle Cell Lymphoma 76 0.025
1000
P HMP002 Hemophagocytic Lymphohistiocytosis 67 0.025
1001
P THY109 Thyroid Cancer, Nonmedullary, 1 64 0.025
1002
CNT047 Contact Dermatitis 64 0.025
1003
HMT002 Hematologic Cancer 64 0.025
1004
SKN019 Skin Melanoma 63 0.025
1005
P CMR001 Camurati-Engelmann Disease 62 0.025
1006
ADR005 Adrenal Carcinoma 59 0.025
1007
GNT003 Genital Herpes 58 0.025
1008
ADN027 Adenomyosis 57 0.025
1009
MYM001 Myoma 56 0.025
1010
STR020 Strabismus 55 0.025
1011
c OVR114 Ovarian Cancer 1 54 0.025
1012
TCD001 Tic Disorder 54 0.025
1013
LPD009 Lipid Storage Disease 53 0.025
1014
ILT001 Ileitis 52 0.025
1015
TLN003 Telangiectasis 52 0.025
1016
ANG018 Angiomyolipoma 50 0.025
1017
SYN005 Synostosis 50 0.025
1018
ASP008 Aspiration Pneumonitis 45 0.025
1019
MYF001 Myofibroma 42 0.025
1020
c SPN310 Spondylocostal Dysostosis 1, Autosomal Recessive 41 0.025
1021
c SZR022 Seizures, Benign Familial Neonatal, 1 39 0.025
1022
PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 35 0.025
1023
c EMR017 Emery-Dreifuss Muscular Dystrophy 1, X-Linked 29 0.025
1024
SPR024 Supratentorial Cancer 26 0.025
1025
PLM028 Pulmonary Coin Lesion 21 0.025
1026
c HMP004 Hemophilia B 67 0.023
1027
c DNG003 Dengue Disease 66 0.023
1028
ADL030 Adult-Onset Still's Disease 65 0.023
1029
ABT001 Abetalipoproteinemia 64 0.023
1030
P ALP009 Alopecia Areata 64 0.023
1031
MNK001 Menkes Disease 64 0.023
1032
P MCH002 Machado-Joseph Disease 63 0.023
1033
P GLL022 Guillain-Barre Syndrome 61 0.023
1034
CHK001 Chikungunya 61 0.023
1035
CCC001 Coccidioidomycosis 60 0.023
1036
SPN027 Spinal Stenosis 60 0.023
1037
P BRN019 Bernard-Soulier Syndrome 60 0.023
1038
P BCK002 Beckwith-Wiedemann Syndrome 58 0.023
1039
CRT002 Cartilage-Hair Hypoplasia 58 0.023
1040
P HYP097 Hyperekplexia 57 0.023
1041
PTT046 Pituitary Hormone Deficiency, Combined, 2 57 0.023
1042
c ACT135 Acute Graft Versus Host Disease 57 0.023
1043
HYP052 Hyperkalemic Periodic Paralysis 57 0.023
1044
P BRN009 Burning Mouth Syndrome 56 0.023
1045
c RHB024 Rhabdomyosarcoma 2 56 0.023
1046
P CPL006 Capillary Hemangioma 56 0.023
1047
NLP001 Nail-Patella Syndrome 56 0.023
1048
P INT070 Intestinal Obstruction 55 0.023
1049
P ERY058 Erythrocytosis, Familial, 1 55 0.023
1050
P FML052 Familial Cold Autoinflammatory Syndrome 55 0.023
1051
P SMP003 Simpson-Golabi-Behmel Syndrome 54 0.023
1052
c INF023 Inflammatory Breast Carcinoma 54 0.023
1053
P LPC002 Lip Cancer 54 0.023
1054
LPR001 Lepromatous Leprosy 53 0.023
1055
ACT098 Acute Erythroid Leukemia 52 0.023
1056
P SHR001 Short Bowel Syndrome 52 0.023
1057
SRT004 Serotonin Syndrome 51 0.023
1058
ADR012 Adrenal Gland Disease 51 0.023
1059
PLS009 Plasma Cell Neoplasm 51 0.023
1060
P PSD015 Pseudohypoparathyroidism 50 0.023
1061
HND002 Hand, Foot and Mouth Disease 50 0.023
1062
MGR001 Migraine Without Aura 47 0.023
1063
PLC001 Placenta Accreta 46 0.023
1064
HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 45 0.023
1065
MCR037 Macroglossia 44 0.023
1066
NRL004 Neuroleptic Malignant Syndrome 44 0.023
1067
c CHR579 Chiari Malformation Type Ii 42 0.023
1068
c VRL005 Viral Pneumonia 42 0.023
1069
KRN001 Korean Hemorrhagic Fever 42 0.023
1070
P HMF004 Hemifacial Spasm 41 0.023
1071
c GLL024 Gallbladder Disease 1 39 0.023
1072
VSM001 Vasomotor Rhinitis 38 0.023
1073
INT046 Intestinal Tuberculosis 37 0.023
1074
P GRM010 Germ Cells Tumors 37 0.023
1075
TTH007 Tooth Erosion 36 0.023
1076
SML011 Smoldering Myeloma 34 0.023
1077
MSN003 Mesenteric Vascular Occlusion 33 0.023
1078
IDP041 Idiopathic Recurrent Pericarditis 32 0.023
1079
MTH021 Methylmalonic Acidemia with Homocystinuria 31 0.023
1080
NTR042 Neutrophilic Dermatosis, Acute Febrile 31 0.023
1081
P HYP729 Hypersensitivity Reaction Disease 31 0.023
1082
c INH004 Inherited Blood Coagulation Disease 29 0.023
1083
c WSK002 Wiskott-Aldrich Syndrome 2 27 0.023
1084
ISC001 Ischemic Neuropathy 26 0.023
1085
ARR048 Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 26 0.023
1086
VNT032 Ventricular Tachycardia, Familial 26 0.023
1087
PRX009 Paroxysmal Hemicrania 25 0.023
1088
c CTS044 Cutis Laxa, Autosomal Recessive, Type Iic 25 0.023
1089
CHR281 Chronic Hiccups 23 0.023
1090
APN006 Apnea of Prematurity 22 0.023
1091
NNF008 Non-Functioning Paraganglioma 17 0.023
1092
c ATR037 Atrial Fibrillation, Familial, 7 17 0.023
1093
c HRN019 Hair-an Syndrome 16 0.023
1094
ACR022 Acardia 13 0.023
1095
CRD022 Cardiomyopathy and Deafness Due to Trna Lysine Gene Mutation 6 0.023
1096
P RTN008 Retinitis Pigmentosa 81 0.020
1097
ESP021 Esophageal Cancer 79 0.020
1098
P WSK001 Wiskott-Aldrich Syndrome 76 0.020
1099
VNH007 Von Hippel-Lindau Syndrome 72 0.020
1100
EWN003 Ewing Sarcoma 72 0.020
1101
LSH001 Leishmaniasis 71 0.020
1102
P NSP012 Nasopharyngeal Carcinoma 71 0.020
1103
SVR004 Severe Combined Immunodeficiency 71 0.020
1104
P TST021 Testicular Germ Cell Tumor 70 0.020
1105
P OST001 Osteopetrosis 70 0.020
1106
c PRM196 Premature Ovarian Failure 1 68 0.020
1107
OTT002 Otitis Media 67 0.020
1108
P NRM001 Neuromyelitis Optica 67 0.020
1109
PLM031 Poliomyelitis 64 0.020
1110
P LNG064 Lung Cancer Susceptibility 3 64 0.020
1111