Search results for "heart block"

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

1444 hits were found for 'heart block'

# Family MCID Name MIFTS Score
1
c HRT021 Heart Block, Progressive, Type Ia 47 7.512
2
c PRG043 Progressive Familial Heart Block, Type Ib 28 6.742
3
P HRT035 Heart Block, Congenital 39 6.713
4
c FML250 Familial Progressive Cardiac Conduction Defect 31 4.951
5
c PRG101 Progressive Familial Heart Block, Type Ii 23 3.962
6
ATR060 Atrial Standstill, Digenic 53 3.809
7
SCN049 Second-Degree Atrioventricular Block 22 3.311
8
P ATR081 Atrial Standstill 30 2.006
9
SNR013 Sino-Auricular Heart Block 4 1.992
10
P HRT032 Heart Disease 76 0.730
11
CNG034 Congestive Heart Failure 71 0.473
12
ISC006 Ischemic Heart Disease 68 0.322
13
P MYC007 Myocardial Infarction 79 0.320
14
RGH001 Right Bundle Branch Block 43 0.310
15
c CRN174 Coronary Heart Disease 2 22 0.291
16
P CRD011 Cardiomyopathy 67 0.279
17
c CRN172 Coronary Heart Disease 3 21 0.274
18
P CRN211 Coronary Artery Disease 75 0.267
19
SYS003 Systolic Heart Failure 43 0.264
20
c CRN175 Coronary Heart Disease 4 21 0.254
21
PRP027 Peripheral Vascular Disease 69 0.252
22
P CRN178 Coronary Heart Disease 6 24 0.245
23
ATR057 Atrioventricular Block 49 0.244
24
DST006 Diastolic Heart Failure 46 0.228
25
END072 Endotheliitis 42 0.227
26
c CRN214 Coronary Heart Disease 5 23 0.225
27
P HYP055 Hypoplastic Left Heart Syndrome 60 0.219
28
ART111 Artery Disease 57 0.217
29
ISC004 Ischemia 59 0.210
30
c PND001 Pain Disorder 55 0.207
31
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 0.201
32
P ATR011 Atrial Fibrillation 64 0.192
33
ART021 Arteriosclerosis 59 0.188
34
c ACT075 Acute Myocardial Infarction 60 0.187
35
HYP006 Hypertensive Heart Disease 50 0.169
36
SNG003 Single Ventricular Heart 24 0.168
37
P NRP001 Neuropathy 60 0.167
38
MSC004 Muscle Tissue Disease 36 0.164
39
P MYP004 Myopathy 67 0.160
40
HRT012 Heart Valve Disease 41 0.159
41
ACR041 Acromelic Frontonasal Dysostosis 46 0.157
42
BRT030 Birth Defects 43 0.157
43
c CRN173 Coronary Heart Disease 8 20 0.155
44
c DLT002 Dilated Cardiomyopathy 75 0.153
45
STR067 Stroke, Ischemic 77 0.150
46
ATH003 Atherosclerosis 62 0.149
47
P RSP003 Respiratory Failure 70 0.148
48
PRP080 Peripheral Artery Disease 36 0.146
49
P MYC008 Myocarditis 54 0.146
50
P ART022 Arthritis 75 0.145
51
P OBS005 Obesity 93 0.143
52
RSP006 Respiratory System Disease 62 0.143
53
P PLM037 Pulmonary Hypertension 79 0.143
54
ATN002 Autonomic Nervous System Disease 47 0.142
55
RHM028 Rheumatic Heart Disease 51 0.142
56
VSC007 Vascular Disease 67 0.142
57
P MSC033 Muscle Disorders 52 0.138
58
P PRP019 Peripheral Nervous System Disease 54 0.138
59
BCK006 Back Pain 42 0.134
60
P BRS047 Breast Cancer 100 0.132
61
P SLP006 Sleep Apnea 61 0.130
62
c CRN177 Coronary Heart Disease 7 22 0.130
63
UNV002 Univentricular Heart 26 0.130
64
P HPT021 Hepatitis 70 0.127
65
RHM001 Rheumatic Fever 50 0.126
66
P CHR345 Chronic Pain 49 0.124
67
SLP005 Sleep Disorder 53 0.124
68
ART017 Aortic Disease 58 0.122
69
VND001 Vein Disease 52 0.122
70
NRN002 Neuronitis 42 0.122
71
P END033 Endocarditis 52 0.122
72
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.121
73
RHM027 Rheumatic Disease 57 0.120
74
HV1006 Hiv-1 82 0.120
75
HRT007 Heart Cancer 50 0.120
76
ANR040 Aneurysm 57 0.119
77
c MYC058 Myocardial Infarction 2 29 0.117
78
NRM005 Neuromuscular Disease 57 0.116
79
CNN005 Connective Tissue Disease 61 0.116
80
IMP003 Impaired Renal Function Disease 37 0.116
81
SYN036 Syncope 47 0.115
82
PHY002 Physical Disorder 44 0.115
83
HYP266 Hypoxia 55 0.115
84
c FML001 Familial Atrial Fibrillation 59 0.114
85
SDD007 Sudden Cardiac Death 46 0.114
86
SPN369 Spinal Disease 41 0.114
87
c HYP595 Hypertension, Essential 69 0.113
88
LNG099 Lung Disease 62 0.113
89
P HRT017 Heart Tumor 35 0.113
90
c AST037 Asthma 1 31 0.112
91
SCR035 Sacral Agenesis with Vertebral Anomalies 33 0.111
92
c CHR089 Chronic Kidney Failure 66 0.111
93
P LPS004 Lupus Erythematosus 63 0.111
94
P VNT002 Ventricular Septal Defect 59 0.111
95
P THY032 Thyroiditis 54 0.110
96
c AST039 Asthma 2 31 0.110
97
INF013 Inferior Myocardial Infarction 37 0.110
98
P HYP086 Hypothyroidism 65 0.109
99
NTR005 Nutritional Deficiency Disease 39 0.108
100
ANG054 Angina Pectoris 51 0.108
101
P NRV006 Nervous System Cancer 62 0.107
102
c ADL079 Adult Heart Tumor 19 0.107
103
P SCK002 Sick Sinus Syndrome 50 0.107
104
c CRN176 Coronary Heart Disease 9 20 0.106
105
P ART023 Arthropathy 63 0.106
106
CRN030 Coronary Stenosis 50 0.105
107
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 60 0.104
108
LRN003 Learning Disability 51 0.104
109
ATN005 Autonomic Dysfunction 45 0.104
110
c CHR096 Chronic Pulmonary Heart Disease 40 0.104
111
PCK002 Pick Disease 67 0.103
112
P LKM002 Leukemia 70 0.103
113
P CLL015 Collagen Disease 49 0.103
114
c CNT015 Central Sleep Apnea 44 0.102
115
CRT057 Critical Congenital Heart Disease 20 0.102
116
P LYM118 Lymphoma 70 0.102
117
P SPS003 Spastic Diplegia 53 0.102
118
URN009 Urinary System Disease 53 0.101
119
BNF002 Bone Fracture 47 0.101
120
PRS047 Prostatitis 56 0.101
121
P URF003 Urofacial Syndrome 1 52 0.101
122
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 47 0.100
123
MNT002 Mental Depression 54 0.100
124
CRD119 Cardiac Arrest 63 0.099
125
END030 End Stage Renal Failure 52 0.099
126
GLC008 Glucose Metabolism Disease 47 0.099
127
P RHM011 Rheumatoid Arthritis 88 0.098
128
ALN001 Aland Island Eye Disease 45 0.098
129
P AST005 Asthma 82 0.098
130
ANX002 Anxiety Disorder 69 0.098
131
CRB031 Cerebral Arterial Disease 31 0.097
132
P ACT080 Acute Pulmonary Heart Disease 32 0.097
133
PRP021 Peripheral Nervous System Neoplasm 50 0.097
134
c ACT071 Acute Kidney Failure 50 0.097
135
MVM001 Movement Disease 54 0.097
136
JNT002 Joint Disorders 56 0.096
137
CRD118 Cardiovascular Cancer 47 0.096
138
P OST012 Osteoarthritis 82 0.095
139
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 55 0.094
140
BLD053 Blood Platelet Disease 46 0.094
141
P PNC044 Pancreatitis 60 0.094
142
GNR004 Generalized Anxiety Disorder 51 0.094
143
PRD011 Proud Syndrome 42 0.093
144
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.093
145
P NRV007 Nervous System Disease 71 0.093
146
c SYS001 Systemic Lupus Erythematosus 87 0.093
147
ALR002 Al-Raqad Syndrome 36 0.093
148
HDC001 Headache 54 0.093
149
CRB009 Cerebritis 38 0.092
150
CRD003 Cardiac Sarcoidosis 43 0.092
151
c BLD124 Bleeding Disorder, Platelet-Type, 11 42 0.091
152
AYM001 Ayme-Gripp Syndrome 45 0.091
153
SNS023 Sensory System Cancer 46 0.090
154
THR099 Third-Degree Atrioventricular Block 30 0.090
155
TTR001 Tetralogy of Fallot 71 0.090
156
P MSC005 Muscular Dystrophy 64 0.090
157
ADJ001 Adjustment Disorder 38 0.090
158
VSC047 Vascular Malformation 45 0.090
159
CPL007 Capillary Malformation-Arteriovenous Malformation 41 0.090
160
PLP001 Pulpitis 47 0.089
161
FRS012 First-Degree Atrioventricular Block 31 0.089
162
DXT001 Dextrocardia 44 0.089
163
P CRD132 Cardiac Conduction Defect 40 0.088
164
P MTR012 Mitral Valve Disease 59 0.087
165
OBS061 Obstructive Sleep Apnea 66 0.087
166
P PRS040 Prostate Cancer 89 0.087
167
VNT011 Ventricular Fibrillation, Familial, 1 43 0.087
168
P LNG032 Lung Cancer 94 0.087
169
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.087
170
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.086
171
ALL026 Allergic Hypersensitivity Disease 53 0.086
172
c ACT076 Acute Myocarditis 42 0.086
173
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.086
174
c TRC078 Trichohepatoenteric Syndrome 2 31 0.086
175
CRB004 Cerebral Artery Occlusion 46 0.085
176
CND002 Conduct Disorder 56 0.085
177
KDS001 Kid Syndrome 53 0.085
178
CSY001 C Syndrome 49 0.085
179
LPD008 Lipid Metabolism Disorder 58 0.084
180
INF034 Infective Endocarditis 50 0.084
181
RNL097 Renal Artery Disease 45 0.084
182
P INF032 Infertility 61 0.084
183
MTH009 Mouth Disease 63 0.084
184
CHL071 Child Syndrome 58 0.084
185
HYD057 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 44 0.084
186
SRC014 Sarcoma 66 0.083
187
TRN044 Transposition of the Great Arteries 47 0.082
188
c ART101 Aortic Valve Disease 2 55 0.082
189
INT007 Intermediate Coronary Syndrome 52 0.082
190
LPD004 Lipoid Nephrosis 48 0.081
191
GDS001 Good Syndrome 45 0.081
192
PRN021 Paranasal Sinus Disease 50 0.081
193
NSL022 Nasal Cavity Disease 42 0.081
194
MSC072 Muscle Cancer 51 0.081
195
PLM129 Pulmonary Disease, Chronic Obstructive 62 0.080
196
ATN004 Autonomic Neuropathy 44 0.080
197
P PNM007 Pneumonia 66 0.080
198
DPH021 Diaphragm Disease 45 0.080
199
PLM033 Pulmonary Embolism 59 0.080
200
WLL006 Wells Syndrome 56 0.079
201
DSS008 Disease of Mental Health 55 0.079
202
BRN080 Brain Ischemia 41 0.079
203
P LVR013 Liver Disease 72 0.079
204
P INF038 Influenza 74 0.078
205
WTH001 Withdrawal Disorder 41 0.078
206
P BRG001 Brugada Syndrome 59 0.078
207
WLF001 Wolff-Parkinson-White Syndrome 57 0.078
208
ADL002 Adult Syndrome 53 0.077
209
PLM010 Pulmonary Edema 56 0.077
210
P RST002 Restrictive Cardiomyopathy 50 0.076
211
P AMY004 Amyloidosis 64 0.076
212
P CRV039 Cervicitis 44 0.076
213
P DYS021 Dysautonomia 47 0.075
214
P PLM040 Pulmonary Valve Disease 45 0.075
215
BLD054 Blood Protein Disease 40 0.075
216
SXL003 Sexual Disorder 47 0.075
217
CRN073 Coronary Arteries Congenital Malformation 13 0.075
218
KRN002 Kearns-Sayre Syndrome 59 0.075
219
TTH006 Tooth Disease 52 0.075
220
HRT008 Heart Conduction Disease 43 0.075
221
END020 Endocardial Fibroelastosis 44 0.075
222
CRN017 Coronary Thrombosis 48 0.075
223
SPC003 Specific Developmental Disorder 40 0.074
224
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.074
225
HPT023 Hepatocellular Carcinoma 91 0.074
226
HYP540 Hypertension, Diastolic 41 0.073
227
P MSC007 Muscle Hypertrophy 59 0.073
228
P MLT019 Multiple Myeloma 80 0.073
229
MDY003 Mody, Type Ii 38 0.073
230
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 24 0.073
231
CRD137 Cardiogenic Shock 46 0.072
232
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 41 0.072
233
P RNL015 Renal Hypertension 47 0.072
234
CRT016 Carotid Artery Disease 55 0.072
235
P ADN016 Adenocarcinoma 69 0.072
236
c CNG031 Congenital Nervous System Abnormality 39 0.071
237
INS024 Insulin-Like Growth Factor I 74 0.071
238
P ENC018 Encephalopathy 59 0.070
239
EXF001 Exfoliation Syndrome 57 0.070
240
c VNT013 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1 49 0.070
241
MRG013 Mirage Syndrome 26 0.070
242
CHG001 Chagas Disease 62 0.069
243
ING001 Inguinal Hernia 57 0.069
244
P PLN008 Peeling Skin Syndrome 47 0.069
245
BNS002 Bone Structure Disease 36 0.069
246
c HPT001 Hepatitis C 68 0.069
247
PRC013 Pericarditis 52 0.069
248
SKN016 Skin Disease 68 0.069
249
c MTR002 Mitral Valve Insufficiency 44 0.069
250
P HYP071 Hypersensitivity Reaction Type Ii Disease 51 0.068
251
CMP010 Complex Regional Pain Syndrome 42 0.068
252
VSC008 Vascular Hemostatic Disease 33 0.068
253
DFC004 Deficiency Anemia 65 0.068
254
P NNT042 Neonatal Lupus Erythematosus 35 0.068
255
CTS003 Coats Disease 57 0.067
256
RDN001 Reading Disorder 39 0.067
257
MDS022 Mediastinitis 41 0.067
258
BRN071 Brain Injury 52 0.066
259
ANX004 Anoxia 44 0.065
260
P EPL164 Epilepsy 66 0.065
261
P MYT002 Myotonic Dystrophy 47 0.065
262
SKN023 Skin Tag 46 0.065
263
MYX004 Myxedema 38 0.065
264
MLR004 Malaria 79 0.065
265
HYP066 Hyperglycemia 60 0.065
266
P CLR023 Colorectal Cancer 97 0.064
267
VSC006 Vascular Cancer 54 0.064
268
c HPT073 Hepatitis C Virus 72 0.064
269
c ART115 Aortic Valve Disease 1 53 0.064
270
ART016 Aortic Aneurysm 67 0.064
271
PRC012 Pericardial Effusion 50 0.064
272
TBR010 Tuberculosis 69 0.064
273
THY030 Thyroid Gland Disease 51 0.063
274
SKN027 Skin Conditions 45 0.063
275
VSC009 Vascular Skin Disease 22 0.063
276
HTR003 Heterotaxy 42 0.063
277
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 26 0.063
278
MYC005 Myocardial Stunning 44 0.062
279
CRT015 Carotid Artery Occlusion 43 0.062
280
PNM008 Pneumothorax 52 0.062
281
CRD001 Cardiac Tamponade 44 0.062
282
c ATM022 Autoimmune Myocarditis 41 0.062
283
PRP009 Peripartum Cardiomyopathy 41 0.062
284
P PLY019 Polyneuropathy 54 0.062
285
FML039 Female Reproductive System Disease 48 0.062
286
HYP005 Hypokalemia 51 0.062
287
OVR063 Overnutrition 49 0.062
288
BRS051 Breast Disease 62 0.062
289
MLR007 Male Reproductive System Disease 37 0.062
290
MYC002 Mycobacterium Avium Complex Disease 51 0.062
291
P HLT001 Holt-Oram Syndrome 58 0.061
292
ISC005 Ischemic Bone Disease 38 0.061
293
P HRP006 Herpes Simplex 65 0.061
294
P HYP076 Hyperthyroidism 56 0.061
295
ATR024 Atrial Fibrillation and Stroke 22 0.061
296
P FML035 Familial Hyperlipidemia 50 0.061
297
ACD009 Acid-Labile Subunit, Deficiency of 48 0.060
298
UPP004 Upper Respiratory Tract Disease 48 0.060
299
P SHR029 Short Syndrome 60 0.060
300
c PLM128 Pulmonary Hypertension, Primary, 2 30 0.060
301
PNC034 Pancreas Disease 57 0.060
302
c DYS033 Dysautonomia Like Disorder 19 0.060
303
BRN028 Brain Cancer 70 0.060
304
GNT019 Giant Cell Myocarditis 31 0.060
305
P BLD051 Blood Coagulation Disease 45 0.060
306
WST001 West Syndrome 61 0.060
307
P MCR129 Microvascular Complications of Diabetes 1 57 0.059
308
P CTR002 Cataract 57 0.059
309
PLC008 Placenta Disease 36 0.059
310
RPR002 Reproductive System Disease 46 0.059
311
TRC062 Tricuspid Atresia 34 0.059
312
PRT036 Peritonitis 62 0.059
313
c RNL016 Renal Infectious Disease 24 0.059
314
P OVR042 Ovarian Cancer 75 0.059
315
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.058
316
PST028 Post-Traumatic Stress Disorder 57 0.058
317
MDD011 Mood Disorder 61 0.058
318
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.058
319
P PRD008 Periodontitis 46 0.058
320
DBT002 Diabetic Autonomic Neuropathy 42 0.058
321
SNT004 Sinoatrial Node Dysfunction and Deafness 27 0.058
322
c OST147 Osteoarthritis 1 33 0.058
323
PRP050 Peripheral Arterial Occlusive Disease 1 17 0.058
324
c CNT035 Central Nervous System Disease 59 0.057
325
GST053 Gastric Cancer 77 0.057
326
ETN001 Eating Disorder 60 0.057
327
P LFT003 Left Ventricular Noncompaction 49 0.057
328
NSD001 Nose Disease 52 0.057
329
CCN007 Cocoon Syndrome 35 0.057
330
P SKN013 Skin Benign Neoplasm 46 0.057
331
DWN001 Down Syndrome 65 0.057
332
CPL005 Capillary Disease 40 0.057
333
PHR003 Pharyngitis 58 0.056
334
P DBT005 Diabetes Insipidus 53 0.056
335
c THR092 Thrombophilia Due to Thrombin Defect 56 0.056
336
CRB087 Cerebral Arteriosclerosis 24 0.056
337
P NRB001 Neuroblastoma 69 0.056
338
P INT070 Intestinal Obstruction 56 0.056
339
c PLN018 Peeling Skin Syndrome 2 35 0.056
340
CRB025 Carbohydrate Metabolic Disorder 47 0.056
341
PST053 Postherpetic Neuralgia 41 0.056
342
CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 43 0.056
343
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 44 0.055
344
c PNC106 Pancreatic Agenesis 1 40 0.055
345
LFT009 Left Ventricular Outflow Tract Obstruction 44 0.055
346
P THR014 Thrombocytopenia 64 0.055
347
CHN016 Cohen Syndrome 55 0.055
348
c HPT016 Hepatitis B 64 0.055
349
ATN003 Autonomic Nervous System Neoplasm 43 0.055
350
BRS090 Breast Reconstruction 39 0.055
351
HDN002 Head Injury 45 0.055
352
NSY001 N Syndrome 39 0.055
353
P PHC003 Pheochromocytoma 71 0.055
354
FBR012 Fabry Disease 69 0.055
355
c PLM022 Pulmonary Valve Insufficiency 38 0.055
356
ATM052 Autoimmune Disease 1 28 0.055
357
RTN023 Retinitis 49 0.054
358
FCL011 Facial Nerve Disease 38 0.054
359
ART005 Arteriovenous Malformation 65 0.054
360
GLT021 Glutaricaciduria, Type I 48 0.054
361
HRT029 Heart Tumor of the Child 17 0.054
362
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 55 0.054
363
GNG013 Gingivitis 60 0.054
364
ACT084 Acute Stress Disorder 40 0.054
365
P INT068 Intestinal Disease 61 0.054
366
P MSC003 Muscular Atrophy 51 0.054
367
SPN041 Spinal Cord Disease 48 0.054
368
PLM041 Pulmonary Valve Stenosis 48 0.054
369
BLD044 Bladder Disease 51 0.054
370
SPN051 Spondylitis 50 0.054
371
EBS001 Ebstein Anomaly 44 0.053
372
SNS003 Sensory Peripheral Neuropathy 47 0.053
373
P HYP265 Hypotonia 39 0.053
374
PRM025 Primary Bacterial Infectious Disease 43 0.053
375
IMM136 Immune System Disease 50 0.053
376
WLS001 Wilson Disease 72 0.053
377
P TRC087 Tricuspid Valve Disease 44 0.053
378
PSY004 Psychotic Disorder 67 0.053
379
MSS002 Mass Syndrome 59 0.053
380
P TRC086 Trichohepatoenteric Syndrome 1 46 0.053
381
CRB085 Cerebral Hemorrhage 43 0.053
382
GNC005 Geniculate Ganglionitis 31 0.052
383
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 29 0.052
384
CRC006 Carcinoid Syndrome 51 0.052
385
HRT011 Heart Septal Defect 41 0.052
386
CRT028 Cor Triatriatum 21 0.052
387
PRS036 Parasitic Protozoa Infectious Disease 45 0.052
388
CNV002 Conversion Disorder 42 0.052
389
BRN106 Burns 52 0.052
390
VSC011 Vasculitis 62 0.052
391
P VNS003 Venous Insufficiency 53 0.052
392
CYT008 Cytomegalovirus Infection 51 0.052
393
c PST001 Posterior Myocardial Infarction 32 0.051
394
PLY023 Polycystic Liver Disease 57 0.051
395
MNN017 Mononeuropathy 40 0.051
396
GLB001 Gilbert Syndrome 61 0.051
397
DBT087 Diabetes Insipidus, Neurohypophyseal 59 0.051
398
HRT006 Heart Aneurysm 26 0.051
399
PRS042 Prostate Disease 52 0.051
400
P EXN002 Exanthem 57 0.051
401
c ACT210 Acute Respiratory Distress Syndrome 57 0.051
402
C3D001 C3 Deficiency 53 0.051
403
STM006 Stomach Disease 50 0.051
404
c PLN021 Peeling Skin Syndrome 3 31 0.051
405
HYP056 Hypoglycemia 61 0.050
406
P PRX010 Paroxysmal Ventricular Fibrillation 39 0.050
407
ATM053 Autoimmune Disease 2 19 0.050
408
HYD012 Hydrops Fetalis 44 0.050
409
CNG134 Congenitally Corrected Transposition of the Great Arteries 23 0.050
410
c MCL062 Mucolipidosis Ii Alpha/beta 60 0.049
411
ALC010 Alcoholic Cardiomyopathy 38 0.049
412
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 36 0.049
413
P PLM036 Pulmonary Fibrosis 68 0.049
414
BRC012 Brucellosis 65 0.049
415
ACT017 Acute Chest Syndrome 48 0.049
416
c PLM121 Pulmonary Hypertension, Primary, 4 29 0.049
417
GST050 Gastrointestinal System Disease 54 0.049
418
P MMB011 Membranous Nephropathy 56 0.049
419
NRR001 Neuroretinitis 42 0.049
420
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 34 0.049
421
c PLN017 Peeling Skin Syndrome 1 33 0.049
422
DMN002 Dementia 64 0.049
423
c SBC003 Subacute Bacterial Endocarditis 35 0.049
424
CLT003 Colitis 59 0.049
425
CNS004 Constipation 57 0.049
426
SML033 Small Cell Cancer of the Lung, Somatic 53 0.049
427
BCK001 Becker Muscular Dystrophy 68 0.049
428
PLR022 Pleural Disease 52 0.048
429
PRD007 Periodontal Disease 43 0.048
430
AND005 Androgen Insensitivity Syndrome, Mild 16 0.048
431
FML037 Female Breast Cancer 51 0.048
432
ADR038 Adermatoglyphia 48 0.048
433
ART012 Aortitis 31 0.048
434
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.048
435
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 44 0.048
436
ADR005 Adrenal Carcinoma 56 0.048
437
ALL006 Allergic Asthma 58 0.048
438
P ALX003 Alexander Disease 64 0.048
439
c LNG044 Long Qt Syndrome 1 67 0.048
440
ANG049 Angioedema Induced by Ace Inhibitors 35 0.048
441
SBC016 Subacute Delirium 27 0.048
442
P SYS005 Systemic Scleroderma 58 0.047
443
CRB008 Cerebral Atherosclerosis 43 0.047
444
SXD001 Sex Differentiation Disease 40 0.047
445
SNT005 Sinoatrial Node Disease 35 0.047
446
ATR055 Atrial Septal Aneurysm 24 0.047
447
ACT094 Acute Articular Rheumatism 21 0.047
448
P INT143 Interstitial Cystitis 57 0.047
449
CRB037 Cerebral Palsy 54 0.047
450
P ART084 Arteriovenous Fistula 44 0.047
451
P ATR001 Atrioventricular Septal Defect 52 0.047
452
P ART106 Arterial Calcification, Generalized, of Infancy, 1 49 0.047
453
MTB004 Metabolic Acidosis 48 0.047
454
CYS001 Cystic Fibrosis 86 0.047
455
P KDN017 Kidney Cancer 67 0.047
456
P HNT016 Huntington Disease 80 0.046
457
HMS001 Hemosiderosis 45 0.046
458
PRN037 Prinzmetal's Variant Angina 40 0.046
459
LYM017 Lyme Disease 63 0.046
460
c HPT003 Hepatitis a 59 0.046
461
P SZR006 Seizure Disorder 57 0.046
462
P GLL020 Gallbladder Disease 59 0.046
463
ATM054 Autoimmune Disease 3 18 0.046
464
LMB062 Limb Ischemia 48 0.046
465
IRN002 Iron Metabolism Disease 43 0.046
466
RFL001 Reflex Sympathetic Dystrophy 48 0.046
467
MTR007 Motor Peripheral Neuropathy 43 0.046
468
P UTR038 Uterine Disease 40 0.046
469
P GST049 Gastrointestinal System Cancer 60 0.046
470
P LRY019 Laryngitis 55 0.046
471
SPS057 Spasticity 42 0.046
472
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 23 0.046
473
DBT010 Diabetic Neuropathy 55 0.046
474
SPN186 Spinal Cord Injury 62 0.046
475
P ATX004 Ataxia 53 0.046
476
GNR003 Generalized Atherosclerosis 38 0.045
477
CRD016 Cardiac Rupture 34 0.045
478
FNT004 Fainting 33 0.045
479
LKC003 Leukocyte Disease 47 0.045
480
ATP002 Atopy 63 0.045
481
P EMR001 Emery-Dreifuss Muscular Dystrophy 53 0.045
482
c ACT134 Acute Liver Failure 50 0.045
483
P MYL006 Myeloid Leukemia 67 0.045
484
THY028 Thyroid Cancer 68 0.045
485
END038 Endocrine Pancreas Disease 43 0.045
486
URT001 Urethritis 40 0.045
487
P RHN004 Rhinitis 61 0.045
488
ADT003 Auditory System Disease 51 0.045
489
P ANR007 Anorexia Nervosa 63 0.044
490
P ESP024 Esophagitis 62 0.044
491
P ADL010 Adult Respiratory Distress Syndrome 60 0.044
492
ACT174 Acute Peripheral Arterial Occlusion 17 0.044
493
RNL001 Renal Artery Obstruction 32 0.044
494
CRC034 Carcinoma Showing Thymus-Like Differentiation 22 0.044
495
c SVR001 Severe Acute Respiratory Syndrome 57 0.044
496
P SPN301 Spinocerebellar Ataxia 2 63 0.044
497
BRN002 Bronchiolitis 56 0.044
498
ATM013 Autoimmune Disease of Cardiovascular System 15 0.044
499
CHL123 Chlamydia 59 0.044
500
P PLY006 Polydactyly 55 0.044
501
PTN001 Patent Foramen Ovale 54 0.044
502
P GRV001 Graves' Disease 61 0.043
503
MGR028 Migraine with or Without Aura 1 50 0.043
504
FRZ001 Frozen Shoulder 44 0.043
505
P SCH015 Schizophrenia 76 0.043
506
P HMN010 Hemangioma 60 0.043
507
SCK005 Sickle Cell Disease 49 0.043
508
CLV009 Clove Syndrome, Somatic 42 0.043
509
P HYP040 Hypospadias 57 0.043
510
PHC013 Phaeochromocytoma 41 0.043
511
ATM005 Autoimmune Disease of Musculoskeletal System 16 0.043
512
WLL001 Williams-Beuren Syndrome 61 0.043
513
P PTN002 Patent Ductus Arteriosus 52 0.043
514
P CRN074 Coronary Artery Aneurysm 44 0.043
515
SPR035 Superior Vena Cava Syndrome 32 0.043
516
P MYS003 Myasthenia Gravis 65 0.043
517
TRC026 Tracheal Disease 35 0.043
518
OCL006 Ocular Hypertension 48 0.043
519
RNL077 Renal Fibrosis 47 0.043
520
P CLC005 Celiac Disease 67 0.043
521
P NPH009 Nephrolithiasis 60 0.043
522
P GLM007 Glomerulonephritis 56 0.043
523
SCK003 Sickle Cell Anemia 68 0.043
524
LVR012 Liver Cirrhosis 67 0.043
525
P RNL014 Renal Cell Carcinoma 81 0.043
526
RHB003 Rhabdomyosarcoma 58 0.043
527
HRP004 Herpes Zoster 56 0.043
528
P THL005 Thalassemia 61 0.042
529
GLC003 Glucose Intolerance 55 0.042
530
c TRC022 Tricuspid Valve Insufficiency 34 0.042
531
HMP001 Hemopericardium 32 0.042
532
BRN038 Bronchial Disease 54 0.042
533
DRG003 Drug Dependence 53 0.042
534
P ENC004 Encephalitis 61 0.042
535
CHL067 Cholecystitis 56 0.042
536
ATN001 Autonomic Peripheral Neuropathy 20 0.042
537
NWC001 Newcastle Disease 54 0.042
538
BND014 Bone Development Disease 42 0.042
539
ACR002 Acrocapitofemoral Dysplasia 36 0.042
540
P ASP006 Aspergillosis 60 0.042
541
FCT008 Factitious Disorder 43 0.042
542
DRG001 Drug Psychosis 40 0.042
543
P SML001 Small Cell Carcinoma 57 0.041
544
P CHR071 Charcot-Marie-Tooth Disease 66 0.041
545
P BCL006 B-Cell Lymphomas 64 0.041
546
P MNN013 Meningitis 65 0.041
547
P CNJ013 Conjunctivitis 65 0.041
548
MRB003 Morbid Obesity 58 0.041
549
SNS001 Sensorineural Hearing Loss 57 0.041
550
P ARC016 Auriculocondylar Syndrome 1 44 0.041
551
BRN055 Bronchogenic Cyst 27 0.041
552
P GNR027 Generalized Peeling Skin Syndrome 22 0.041
553
c SHR030 Short Qt Syndrome 43 0.041
554
PST055 Postural Hypotension 37 0.041
555
HTR014 Heterotaxy, Visceral, 1, X-Linked 35 0.040
556
MYT011 Myotonia 40 0.040
557
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 38 0.040
558
c ATM093 Autoimmune Disease of Peripheral Nervous System 35 0.040
559
P NRP037 Neuropathy, Hereditary Sensory and Autonomic, Type V 57 0.040
560
c OST112 Osteoarthritis-5 40 0.040
561
DCH001 Duchenne Muscular Dystrophy 80 0.040
562
P ANT006 Antiphospholipid Syndrome 58 0.040
563
INT066 Interstitial Lung Disease 58 0.040
564
CLC006 Calcinosis 49 0.040
565
c ATR075 Atrial Fibrillation 15 25 0.040
566
c PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 45 0.039
567
P SPN046 Spinal Muscular Atrophy 63 0.039
568
DRM006 Dermatitis 61 0.039
569
P SPN052 Spondyloarthropathy 60 0.039
570
ADM013 Adamantinoma of Long Bones 59 0.039
571
PRP030 Purpura 59 0.039
572
GST023 Gastric Ulcer 55 0.039
573
P HMR012 Hemorrhagic Fever 55 0.039
574
P PLM085 Pulmonary Hemosiderosis 44 0.039
575
c CHR431 Chronic Venous Insufficiency 44 0.039
576
c CRD099 Cardiomyopathy, Dilated, 1e 42 0.039
577
P ADD001 Addison's Disease 62 0.039
578
ESP023 Esophageal Disease 53 0.039
579
QDR001 Quadriplegia 52 0.039
580
STM007 Stomatitis 50 0.039
581
MLR006 Male Reproductive Organ Cancer 47 0.039
582
CLN019 Colonic Disease 50 0.039
583
SPT001 Septal Myocardial Infarction 16 0.039
584
P OCY001 Oocyte Maturation Defect 39 0.039
585
GST045 Gastroenteritis 60 0.039
586
c CNG006 Congenital Hypothyroidism 59 0.039
587
BNC003 Bone Cancer 45 0.039
588
CRB086 Cerebral Aneurysms 39 0.039
589
ACR007 Acromegaly 65 0.039
590
HPR003 Heparin-Induced Thrombocytopenia 46 0.039
591
INT309 Intellectual Developmental Disorder with Persistence of Fetal Hemoglobin 29 0.039
592
END074 Endocardium Disease 26 0.039
593
P PLY011 Polycystic Ovary Syndrome 66 0.039
594
BRN024 Bronchitis 63 0.039
595
TRM010 Traumatic Brain Injury 52 0.039
596
c CRD093 Cardiomyopathy, Dilated, 1a 38 0.039
597
ATM012 Autoimmune Disease of Blood 37 0.039
598
DXR001 Doxorubicin Induced Cardiomyopathy 36 0.039
599
END035 Endocrine Gland Cancer 52 0.039
600
BLR006 Biliary Tract Disease 51 0.039
601
URT004 Urethral Syndrome 48 0.039
602
CLS010 Cluster Headache 45 0.039
603
OCC004 Occlusion of Gallbladder 16 0.039
604
TRN015 Transient Cerebral Ischemia 56 0.038
605
c INF067 Inflammatory Bowel Disease 10 51 0.038
606
c HYP073 Hypersensitivity Reaction Type Iv Disease 45 0.038
607
P ABD003 Abdominal Aortic Aneurysm 43 0.038
608
ATM014 Autoimmune Disease of Endocrine System 37 0.038
609
HDG012 Hodgkin Lymphoma 73 0.038
610
PRT037 Pertussis 64 0.038
611
TTN003 Tetanus 61 0.038
612
DPH001 Diphtheria 58 0.038
613
P MYS005 Myositis 56 0.038
614
GNG011 Gingival Disease 51 0.038
615
PRP028 Peripheral Vertigo 41 0.038
616
ADR009 Adrenal Cortex Disease 41 0.038
617
CNT017 Central Nervous System Origin Vertigo 28 0.038
618
ART013 Aortic Malignant Tumor 16 0.038
619
WRN001 Werner Syndrome 67 0.038
620
FTT001 Fatty Liver Disease 60 0.038
621
RBR001 Roberts Syndrome 59 0.038
622
P ATR010 Atrial Heart Septal Defect 43 0.038
623
PLS010 Plasma Protein Metabolism Disease 38 0.038
624
CRN006 Coronary Aneurysm 32 0.038
625
CNT098 Central Core Disease 66 0.037
626
P HMR003 Hemorrhagic Disease 57 0.037
627
P LMY004 Leiomyosarcoma 53 0.037
628
P LPS002 Liposarcoma 50 0.037
629
PLM068 Pulmonary Vein Stenosis 39 0.037
630
DXT002 Dextrocardia with Situs Inversus 38 0.037
631
PST048 Postural Orthostatic Tachycardia Syndrome 28 0.037
632
HSB001 His Bundle Tachycardia 22 0.037
633
PLS006 Plasmodium Vivax Malaria 53 0.037
634
HND003 Hand-Foot-Uterus Syndrome 47 0.037
635
P DMY001 Demyelinating Polyneuropathy 43 0.037
636
INT040 Intrinsic Asthma 40 0.037
637
GLB003 Globe Disease 35 0.037
638
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 32 0.037
639
P MDL005 Medulloblastoma 77 0.037
640
ALC007 Alcohol Dependence 65 0.037
641
PSR001 Psoriatic Arthritis 64 0.037
642
P OVR049 Ovarian Disease 55 0.037
643
ANK001 Ankylosis 52 0.037
644
DYS073 Dysphagia 49 0.037
645
c CLL013 Cell Type Cancer 48 0.037
646
GST078 Gastrointestinal Allergy 41 0.037
647
ATM059 Autoimmune Disease 6 26 0.037
648
c MYT021 Myotonic Dystrophy 1 62 0.037
649
SBS003 Substance Abuse 56 0.037
650
PRS045 Prostatic Hypertrophy 44 0.037
651
CRT013 Carotid Stenosis 37 0.037
652
RGH009 Right Atrial Isomerism 32 0.037
653
P DYS154 Dystonia 64 0.037
654
ACH001 Acheiropody 45 0.037
655
RCT017 Rectal Disease 39 0.037
656
ALG001 Algoneurodystrophy 35 0.037
657
NRV004 Nerve Compression Syndrome 35 0.037
658
PNC065 Pinched Nerve 13 0.037
659
P OST002 Osteoporosis 64 0.037
660
P TMT001 Timothy Syndrome 56 0.037
661
MRC001 Marchiafava Bignami Disease 50 0.037
662
c PRG106 Progressive Muscular Dystrophy 41 0.037
663
P TRC005 Tracheal Stenosis 38 0.037
664
P PRT013 Portal Hypertension 59 0.036
665
P PTS002 Ptosis 56 0.036
666
TMP001 Temporal Lobe Epilepsy 51 0.036
667
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 47 0.036
668
GND003 Gonadal Disease 43 0.036
669
TXC005 Toxic Shock Syndrome 61 0.036
670
P FBR017 Fibrosarcoma 56 0.036
671
INT002 Intermittent Claudication 56 0.036
672
PLM034 Pulmonary Emphysema 54 0.036
673
BRN004 Brain Edema 51 0.036
674
HPT074 Hepatic Adenoma, Somatic 51 0.036
675
LVC002 Levocardia 18 0.036
676
CHR103 Charge Syndrome 64 0.036
677
TRC021 Tricuspid Valve Stenosis 39 0.036
678
c HMG004 Hemoglobin D Disease 33 0.036
679
VTM003 Vitamin Metabolic Disorder 33 0.036
680
RHM029 Rheumatic Fever-Related Antigen Rheumatic Fever, Acute, Susceptibility to, Included 23 0.036
681
MND006 Mondor Disease 21 0.036
682
ETH011 Ethylmalonic Encephalopathy 59 0.035
683
RCT018 Rectal Neoplasm 55 0.035
684
JPN002 Japanese Encephalitis 54 0.035
685
DCB001 Decubitus Ulcer 44 0.035
686
EPD019 Epidural Neoplasm 35 0.035
687
CML001 Cumulative Trauma Disorders 21 0.035
688
OCL009 Ocular Cancer 62 0.035
689
SPT004 Septic Arthritis 59 0.035
690
INT075 Intracranial Hypertension 53 0.035
691
P PLY041 Polymyositis 51 0.035
692
P LMB006 Limb-Girdle Muscular Dystrophy 50 0.035
693
CHL004 Cholelithiasis 48 0.035
694
IMM127 Immune System Cancer 42 0.035
695
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 39 0.035
696
c SCK017 Sick Sinus Syndrome 1 29 0.035
697
VGS001 Vagus Nerve Disease 20 0.035
698
NRP015 Neuropathy, Congenital Hypomyelinating 56 0.035
699
RSS002 Roussy-Levy Syndrome 52 0.035
700
P ERY008 Erythromelalgia 52 0.035
701
P CMP008 Compartment Syndrome 48 0.035
702
P CHR102 Charcot-Marie-Tooth Neuropathy 43 0.035
703
c PRS116 Prostate Cancer 1 41 0.035
704
ATM055 Autoimmune Disease 4 18 0.035
705
BRN012 Bronchiolitis Obliterans 58 0.035
706
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.035
707
P HYP065 Hyperaldosteronism 51 0.035
708
P DRR001 Diarrhea 51 0.035
709
DBT084 Diabetes Mellitus, Ketosis-Prone 50 0.035
710
CLF001 Cleft Lip 49 0.035
711
c MCR113 Microvascular Complications of Diabetes 3 49 0.035
712
CRS005 Crest Syndrome 47 0.035
713
KDN013 Kidney Hypertrophy 33 0.035
714
P MYM002 Moyamoya Disease 60 0.035
715
P HRD018 Hair Disease 50 0.035
716
ANT005 Anteroseptal Myocardial Infarction 22 0.035
717
P INT030 Intracranial Aneurysm 54 0.035
718
PRM042 Primary Effusion Lymphoma 53 0.035
719
P TRN020 Turner Syndrome 64 0.034
720
P BPL003 Bipolar Disorder 62 0.034
721
PRM097 Primary Immunodeficiency Disease 61 0.034
722
ANG020 Angiosarcoma 52 0.034
723
THL018 Thalassemia Major 42 0.034
724
ART008 Arteriosclerosis Obliterans 42 0.034
725
c VNT028 Ventricular Septal Defect 1 29 0.034
726
PLM001 Pulmonary Tuberculosis 68 0.034
727
P CSH001 Cushing's Syndrome 64 0.034
728
ACH005 Achalasia 54 0.034
729
PRP016 Paraplegia 49 0.034
730
ACT058 Active Peptic Ulcer Disease 46 0.034
731
FBR054 Fibroma 43 0.034
732
VNT001 Ventilation Pneumonitis 37 0.034
733
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 34 0.034
734
c NNT025 Neonatal Systemic Lupus Erythematosus 15 0.034
735
INT253 Intestinal Benign Neoplasm 50 0.034
736
P PSR002 Psoriasis 63 0.034
737
c SPN225 Spondyloarthropathy 1 63 0.034
738
P ALC004 Alcohol Abuse 60 0.034
739
NRN004 Neuroendocrine Tumor 54 0.034
740
RLP001 Relapsing Polychondritis 49 0.034
741
PLS009 Plasma Cell Neoplasm 48 0.034
742
DFF003 Diffuse Scleroderma 41 0.034
743
SCR015 Scarlet Fever 39 0.034
744
ANR010 Aneurysm of Sinus of Valsalva 25 0.034
745
MYT026 Myotonia Atrophica 19 0.034
746
MLT131 Multifocal Atrial Tachycardia 16 0.034
747
P ESN007 Eosinophilia 61 0.033
748
P PRS038 Personality Disorder 61 0.033
749
VRL011 Viral Infectious Disease 59 0.033
750
PLS011 Plasmacytoma 56 0.033
751
P ECL001 Eclampsia 54 0.033
752
MTN003 Motion Sickness 48 0.033
753
CHR028 Chronic Wasting Disease 34 0.033
754
MTC028 Mitochondrial Cardiomyopathy 30 0.033
755
c VNT026 Ventricular Septal Defect 2 23 0.033
756
PRM053 Primary Release Disorder of Platelets 14 0.033
757
ALL003 Allergic Rhinitis 64 0.033
758
ADR012 Adrenal Gland Disease 49 0.033
759
CRV043 Cervical Dystonia 44 0.033
760
DSS010 Dissociative Disorder 35 0.033
761
CMB002 Combat Disorder 24 0.033
762
P PLR004 Pleuropulmonary Blastoma 64 0.033
763
P ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 60 0.033
764
APP008 Appendicitis 60 0.033
765
SMT006 Somatoform Disorder 53 0.033
766
LMY002 Leiomyoma 42 0.033
767
c CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 37 0.033
768
CRV069 Cervix Disease 34 0.033
769
PHN003 Phenylketonuria 73 0.032
770
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.032
771
GST037 Gastroparesis 53 0.032
772
P MTH007 Methemoglobinemia 45 0.032
773
c HYP072 Hypersensitivity Reaction Type Iii Disease 41 0.032
774
ABR009 Abruzzo-Erickson Syndrome 40 0.032
775
CRN265 Craniofacial Malformations, Asymmetric, with Polysyndactyly and Abnormal Skin and Gut Development 34 0.032
776
c CRD199 Cardiomyopathy, Hypertrophic 6 31 0.032
777
YNG002 Young Syndrome 26 0.032
778
ATR076 Atrophic Muscular Disease 18 0.032
779
P HRD008 Hereditary Hemorrhagic Telangiectasia 71 0.032
780
P SDD001 Sudden Infant Death Syndrome 61 0.032
781
P GLY013 Glycogen Storage Disease 59 0.032
782
PMS001 Poems Syndrome 55 0.032
783
P JRV003 Jervell and Lange-Nielsen Syndrome 52 0.032
784
P RNV001 Renovascular Hypertension 47 0.032
785
c VNT024 Ventricular Septal Defect 3 25 0.032
786
c BRG009 Brugada Syndrome 7 25 0.032
787
c CNG148 Congenital Heart Disease, Atrial Septal Defect 19 0.032
788
MLT021 Multiple System Atrophy 71 0.032
789
TST021 Testicular Germ Cell Tumor 70 0.032
790
EWN003 Ewing Sarcoma 64 0.032
791
DNG002 Dengue Hemorrhagic Fever 62 0.032
792
c HPT007 Hepatitis E 54 0.032
793
GTR002 Goiter 54 0.032
794
NRT004 Neuritis 52 0.032
795
GYN001 Gynecomastia 49 0.032
796
AMN002 Amino Acid Metabolic Disorder 48 0.032
797
NWB001 Newborn Respiratory Distress Syndrome 47 0.032
798
PRN011 Pernicious Anemia 46 0.032
799
P KLP003 Klippel-Feil Syndrome 46 0.032
800
MCR103 Microtia 37 0.032
801
c BRG006 Brugada Syndrome 2 33 0.032
802
WRT002 Writing Disorder 29 0.032
803
RSP007 Respiratory Distress Syndrome, Infant 26 0.032
804
MSL001 Measles 61 0.032
805
P BRS044 Breast Adenocarcinoma 60 0.032
806
P TCL004 T-Cell Leukemia 46 0.032
807
SCT001 Sciatic Neuropathy 40 0.032
808
c GLL024 Gallbladder Disease 1 38 0.032
809
LNS003 Lens Disease 38 0.032
810
URT037 Urethral Stricture 33 0.032
811
P APL001 Aplastic Anemia 73 0.031
812
P RFS001 Refsum Disease 62 0.031
813
P HML002 Hemolytic Anemia 60 0.031
814
P DRM010 Dermatomyositis 58 0.031
815
P SYP003 Syphilis 53 0.031
816
NNL002 Nonalcoholic Steatohepatitis 53 0.031
817
SLP001 Sleeping Sickness 48 0.031
818
TRN012 Transient Global Amnesia 39 0.031
819
HRT003 Heart Lymphoma 31 0.031
820
ARR026 Arrhythmogenic Right Ventricular Dysplasia 1 29 0.031
821
RDT005 Radiation Induced Cancer 28 0.031
822
HRT033 Heart-Hand Syndrome, Spanish Type 15 0.031
823
P ALZ034 Alzheimer Disease 93 0.031
824
PLY125 Polycythemia Vera, Somatic 63 0.031
825
TNS005 Tonsillitis 58 0.031
826
P CYS018 Cystitis 53 0.031
827
BNM001 Bone Marrow Cancer 52 0.031
828
BLR001 Biliary Atresia 51 0.031
829
OCL010 Ocular Hypotension 42 0.031
830
MYF002 Myofascial Pain Syndrome 40 0.031
831
P MTC004 Mitochondrial Encephalomyopathy 40 0.031
832
HYP064 Hypogonadotropism 38 0.031
833
INT011 Interstitial Emphysema 38 0.031
834
P ENC011 Encephalomyopathy 34 0.031
835
c SYS038 Systemic Lupus Erythematosus 2 27 0.031
836
c INF055 Infectious Myocarditis 17 0.031
837
c CHR090 Chronic Lymphocytic Leukemia 74 0.030
838
TNG009 Tongue Squamous Cell Carcinoma 74 0.030
839
P LPR003 Leprosy 68 0.030
840
ADR016 Adrenal Cortical Carcinoma 61 0.030
841
CMM005 Common Cold 58 0.030
842
MLG056 Malignant Hyperthermia 57 0.030
843
P BRN120 Bronchus Cancer 46 0.030
844
VGN020 Vaginal Disease 45 0.030
845
c CHR095 Chronic Progressive External Ophthalmoplegia 45 0.030
846
CRP017 Carpal Tunnel Syndrome, Familial 44 0.030
847
P HYP120 Hypoaldosteronism 37 0.030
848
GLS004 Glossopharyngeal Neuralgia 35 0.030
849
FNC005 Functional Colonic Disease 30 0.030
850
MDN002 Median Neuropathy 30 0.030
851
OVR077 Overuse Syndrome 21 0.030
852
RPT005 Repetitive Motion Disorders 18 0.030
853
CNG059 Congenital Arteriovenous Shunt 11 0.030
854
P LYM025 Lymphedema 61 0.030
855
EMB004 Embryonal Carcinoma 56 0.030
856
HPT022 Hepatoblastoma 53 0.030
857
c INF071 Inflammatory Bowel Disease 1 51 0.030
858
FML038 Female Reproductive Organ Cancer 51 0.030
859
CCN001 Cocaine Dependence 48 0.030
860
TRC023 Trichinosis 43 0.030
861
CHR322 Choreoathetosis, Hypothyroidism, and Neonatal Respiratory Distress 41 0.030
862
P MNN007 Meningocele 36 0.030
863
c ADL080 Adult Acute Respiratory Distress Syndrome 23 0.030
864
P ANT001 Anterolateral Myocardial Infarction 20 0.030
865
GRB002 Gerbode Defect 15 0.030
866
DGT004 Digitalis Poisoning 11 0.030
867
ALL009 Allergic Conjunctivitis 51 0.030
868
END080 Endometrial Disease 42 0.030
869
c CLR085 Colorectal Cancer 1 42 0.030
870
c BRN108 Branchiootic Syndrome 1 36 0.030
871
DNT014 Dental Pulp Disease 34 0.030
872
SWL001 Swallowing Disorders 34 0.030
873
BRC011 Brachial Plexus Neuropathy 33 0.030
874
FTD001 Foot Drop 32 0.030
875
HRN022 Hearing Loss/deafness 25 0.030
876
MYL009 Myelodysplastic Syndrome 74 0.029
877
ATT013 Attention Deficit-Hyperactivity Disorder 68 0.029
878
SMT004 Smith-Lemli-Opitz Syndrome 67 0.029
879
TBR024 Tuberous Sclerosis-1 65 0.029
880
P HMP007 Hemophilia 56 0.029
881
P HYP083 Hypopituitarism 52 0.029
882
ESP020 Esophageal Atresia 49 0.029
883
c HMG003 Hemoglobin E Disease 44 0.029
884
NLS001 Nelson Syndrome 43 0.029
885
FXF002 Fox-Fordyce Disease 39 0.029
886
MDY006 Mody, Type Iv 33 0.029
887
GRM003 German Syndrome 24 0.029
888
STR029 Sternal Cleft 18 0.029
889
P HYD006 Hydrocephalus 67 0.029
890
P CRN037 Craniosynostosis 65 0.029
891
CRY002 Cryptorchidism 62 0.029
892
P ORL007 Oral Cavity Cancer 58 0.029
893
HYP020 Hyperprolactinemia 57 0.029
894
ORL011 Oral Cancer 55 0.029
895
HMF006 Hemifacial Microsomia 54 0.029
896
LYM019 Lymphosarcoma 53 0.029
897
P SJG001 Sjogren's Syndrome 53 0.029
898
P PRM006 Primary Biliary Cirrhosis 52 0.029
899
RYS001 Reye Syndrome 51 0.029
900
P OVR046 Ovarian Cyst 50 0.029
901
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 49 0.029
902
OBS001 Obstructive Jaundice 48 0.029
903
PYL006 Pyloric Stenosis 46 0.029
904
LYM116 Lymph Node Disease 44 0.029
905
SPN119 Spondylarthropathy 41 0.029
906
GRM001 Germ Cell and Embryonal Cancer 39 0.029
907
OCL011 Ocular Motility Disease 38 0.029
908
c BRG007 Brugada Syndrome 5 38 0.029
909
c SYS043 Systemic Lupus Erythematosus 1 34 0.029
910
NRL016 Neural Tube Defects 76 0.028
911
LPT001 Leptospirosis 63 0.028
912
APH001 Aphthous Stomatitis 62 0.028
913
c VRL010 Viral Hepatitis 61 0.028
914
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 57 0.028
915
ALP008 Alopecia 55 0.028
916
HYP080 Hypogonadism 54 0.028
917
PLC005 Placental Insufficiency 50 0.028
918
P HML001 Hemolytic-Uremic Syndrome 50 0.028
919
RSP002 Respiratory Syncytial Virus Infectious Disease 48 0.028
920
ANR004 Anuria 46 0.028
921
OLV002 Oliver Syndrome 44 0.028
922
MDY004 Mody, Type Iii 37 0.028
923
MDS018 Mediastinal Cancer 36 0.028
924
HNS001 Hansen's Disease 29 0.028
925
ABS016 Absence of the Pulmonary Artery 19 0.028
926
CRT061 Cor Triatriatum Dexter 16 0.028
927
P ATX030 Ataxia-Telangiectasia 76 0.028
928
GLL018 Gallbladder Cancer 63 0.028
929
HTC002 Hutchinson-Gilford Progeria 62 0.028
930
c ACT073 Acute Leukemia 62 0.028
931
P EHL001 Ehlers-Danlos Syndrome 61 0.028
932
GST092 Gastroesophageal Reflux 61 0.028
933
MLN054 Melanocytic Nevus Syndrome, Congenital, Somatic 58 0.028
934
c INF023 Inflammatory Breast Carcinoma 50 0.028
935
CLL003 Cellulitis 49 0.028
936
PLY020 Polyradiculoneuropathy 44 0.028
937
c LNG050 Long Qt Syndrome 5 43 0.028
938
LNG037 Lung Sarcoma 43 0.028
939
BRN018 Borna Disease 42 0.028
940
RTR001 Retrograde Amnesia 40 0.028
941
CNT067 Central Cord Syndrome 24 0.028
942
LGD001 Leg Dermatosis 19 0.028
943
c TRN008 Transient Arthropathy 15 0.028
944
P LNG064 Lung Cancer Susceptibility 3 62 0.027
945
P SNS014 Sinusitis 60 0.027
946
RTN018 Retinal Disease 56 0.027
947
LNG039 Lung Squamous Cell Carcinoma 52 0.027
948
DBT062 Diabetic Foot Ulcers 52 0.027
949
P LTR001 Lateral Sclerosis 52 0.027
950
BLR007 Biliary Tract Neoplasm 52 0.027
951
TXC002 Toxic Encephalopathy 51 0.027
952
ACL001 Acalculous Cholecystitis 36 0.027
953
WHP002 Whiplash 36 0.027
954
c ATM007 Autoimmune Disease of Central Nervous System 28 0.027
955
PLY039 Polymorphic Reticulosis 19 0.027
956
c GLL026 Gallbladder Disease 3 19 0.027
957
HMT002 Hematologic Cancer 64 0.027
958
c ACT027 Acute Pancreatitis 56 0.027
959
URN010 Urinary Tract Obstruction 56 0.027
960
SPN027 Spinal Stenosis 56 0.027
961
P CTN015 Cutaneous T Cell Lymphoma 50 0.027
962
FCL012 Facial Paralysis 50 0.027
963
HMG002 Hemoglobinuria 49 0.027
964
HYP043 Hyperandrogenism 48 0.027
965
BCT015 Bacteremia 48 0.027
966
CHL061 Childhood Leukemia 48 0.027
967
P THY054 Thyrotoxic Periodic Paralysis 47 0.027
968
PLR006 Pleural Cancer 46 0.027
969
CVR006 Cavernous Hemangioma 46 0.027
970
ISC002 Ischemic Optic Neuropathy 46 0.027
971
RYN001 Raynaud Disease 44 0.027
972
VGN023 Vaginitis 42 0.027
973
P CNT036 Central Nervous System Germ Cell Tumor 39 0.027
974
MNN021 Meningococcemia 38 0.027
975
c MYP072 Myopathy, Myofibrillar, 1 38 0.027
976
FNC006 Functional Gastric Disease 34 0.027
977
P CNT044 Central Nervous System Primitive Neuroectodermal Neoplasm 33 0.027
978
IMM062 Immunodeficiency 11 27 0.027
979
c SYS046 Systemic Lupus Erythematosus 3 24 0.027
980
MTR031 Motor Neuro-Ophthalmic Disorders 23 0.027
981
WLD005 Wild Type Attr Amyloidosis 21 0.027
982
CYN003 Cyanide Poisoning 20 0.027
983
c ADL022 Adult Central Nervous System Primitive Neuroectodermal Neoplasm 19 0.027
984
c CNT032 Central Nervous System Adult Germ Cell Tumor 18 0.027
985
P PRK057 Parkinson Disease, Late-Onset 72 0.026
986
P OST005 Osteogenesis Imperfecta 67 0.026
987
c GLY008 Glycogen Storage Disease Ii 61 0.026
988
P OCL013 Oculodentodigital Dysplasia 59 0.026
989
c SRC025 Sarcoidosis 1 58 0.026
990
CHL068 Cholestasis 58 0.026
991
P PRC031 Preeclampsia/eclampsia 1 57 0.026
992
GLL022 Guillain-Barre Syndrome 56 0.026
993
P BDD001 Budd-Chiari Syndrome 56 0.026
994
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 54 0.026
995
BLM002 Bulimia Nervosa 54 0.026
996
P PYL005 Pyelonephritis 52 0.026
997
LYM024 Lymphatic System Disease 50 0.026
998
PRT038 Protein-Energy Malnutrition 49 0.026
999
SLV003 Salivary Gland Disease 49 0.026
1000
BRN056 Bronchopulmonary Dysplasia 49 0.026
1001
PTT009 Pituitary Gland Disease 48 0.026
1002
c CNG027 Congenital Hemolytic Anemia 48 0.026
1003
P ADM011 Adams-Oliver Syndrome 48 0.026
1004
PLY012 Polyhydramnios 47 0.026
1005
UND005 Undifferentiated Pleomorphic Sarcoma 43 0.026
1006
c BRG005 Brugada Syndrome 1 42 0.026
1007
HMT018 Hematopoietic Stem Cell Transplantation 41 0.026
1008
NNT024 Neonatal Stroke 37 0.026
1009
c SRC023 Sarcoidosis 2 33 0.026
1010
ISC001 Ischemic Neuropathy 33 0.026
1011
THY001 Thyroid Crisis 30 0.026
1012
c MJR007 Major Affective Disorder 1 28 0.026
1013
PRM008 Parametritis 27 0.026
1014
c BRG003 Brugada Syndrome 3 26 0.026
1015
HNM002 Hinman Syndrome 25 0.026
1016
c BRG004 Brugada Syndrome 4 22 0.026
1017
c SCK022 Sick Sinus Syndrome 3 22 0.026
1018
FDL001 Fiedler's Myocarditis 22 0.026
1019
c ATR064 Atrioventricular Septal Defect 3 17 0.026
1020
MYX011 Myxozoa 16 0.026
1021
BNJ001 Benjamin Syndrome 12 0.026
1022
OTT002 Otitis Media 66 0.025
1023
PTR006 Peters Anomaly 64 0.025
1024
P TMP003 Temporal Arteritis 60 0.025
1025
P MYP006 Myopia 59 0.025
1026
c MSC124 Muscular Dystrophy, Congenital 57 0.025
1027
YLL002 Yellow Fever 57 0.025
1028
P CHN012 Chondrosarcoma 57 0.025
1029
P SCL018 Scoliosis 56 0.025
1030
P LYM033 Lymphoproliferative Syndrome 53 0.025
1031
CYS005 Cysticercosis 52 0.025
1032
PST095 Post-Thrombotic Syndrome 50 0.025
1033
P CHL066 Cholangitis 49 0.025
1034
c INH020 Inherited Metabolic Disorder 49 0.025
1035
CHR056 Chronic Tic Disorder 49 0.025
1036
P HMR005 Hemorrhoid 48 0.025
1037
SPN035 Spindle Cell Sarcoma 47 0.025
1038
SKL014 Skeletal Dysplasia 46 0.025
1039
DWR001 Dwarfism 46 0.025
1040
NPH003 Nephrocalcinosis 46 0.025
1041
SKL017 Skeletal Dysplasias 45 0.025
1042
c THR054 Thrombotic Thrombocytopenic Purpura, Familial 44 0.025
1043
HYP085 Hypothalamic Disease 44 0.025
1044
DNG001 Dengue Shock Syndrome 43 0.025
1045
BSL008 Basal Ganglia Disease 43 0.025
1046
SKL003 Skeletal Muscle Cancer 41 0.025
1047
P HYP009 Hypertrophic Pyloric Stenosis 41 0.025
1048
BNR001 Bone Remodeling Disease 40 0.025
1049
HYL004 Hyaline Fibromatosis Syndrome 39 0.025
1050
PRS023 Pearson Syndrome 36 0.025
1051
VSL002 Visual Epilepsy 32 0.025
1052
PDT040 Pediatric Hypertension 31 0.025
1053
ATM016 Autoimmune Disease of Skin and Connective Tissue 31