Search results for "heart block"

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

1274 hits were found for 'heart block'

# Family MCID Name MIFTS Score
1
c HRT021 Heart Block, Progressive, Type Ia 46 7.323
2
P HRT035 Heart Block, Congenital 40 7.056
3
c PRG043 Progressive Familial Heart Block, Type Ib 26 6.331
4
c FML250 Familial Progressive Cardiac Conduction Defect 32 5.016
5
c PRG101 Progressive Familial Heart Block, Type Ii 23 4.014
6
SCN049 Second-Degree Atrioventricular Block 22 3.350
7
ATR060 Atrial Standstill, Digenic 51 3.246
8
P ATR081 Atrial Standstill 29 2.040
9
SNR013 Sino-Auricular Heart Block 4 2.012
10
P HRT032 Heart Disease 64 0.646
11
c CNG401 Congenital Heart Disease 67 0.502
12
CNG034 Congestive Heart Failure 72 0.471
13
RGH001 Right Bundle Branch Block 43 0.351
14
P MYC007 Myocardial Infarction 80 0.336
15
ISC006 Ischemic Heart Disease 54 0.321
16
P CRD011 Cardiomyopathy 66 0.288
17
P CRN211 Coronary Artery Disease 74 0.282
18
c CRN174 Coronary Heart Disease 2 19 0.279
19
ATR057 Atrioventricular Block 49 0.274
20
c CRN172 Coronary Heart Disease 3 19 0.268
21
SYS003 Systolic Heart Failure 42 0.265
22
PRP027 Peripheral Vascular Disease 69 0.262
23
c CRN175 Coronary Heart Disease 4 19 0.260
24
P CRN178 Coronary Heart Disease 6 22 0.246
25
END072 Endotheliitis 41 0.244
26
ART111 Artery Disease 56 0.232
27
DST006 Diastolic Heart Failure 45 0.228
28
c PND001 Pain Disorder 53 0.227
29
c CRN214 Coronary Heart Disease 5 22 0.226
30
P HYP055 Hypoplastic Left Heart Syndrome 60 0.219
31
ISC004 Ischemia 56 0.218
32
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 0.205
33
P ATR011 Atrial Fibrillation 63 0.202
34
c ACT075 Acute Myocardial Infarction 61 0.200
35
VSC007 Vascular Disease 51 0.198
36
ART021 Arteriosclerosis 59 0.191
37
P NRP001 Neuropathy 57 0.180
38
SNG003 Single Ventricular Heart 23 0.173
39
HYP006 Hypertensive Heart Disease 49 0.167
40
c DLT002 Dilated Cardiomyopathy 75 0.166
41
P ART022 Arthritis 73 0.166
42
P MYP004 Myopathy 67 0.161
43
HRT012 Heart Valve Disease 39 0.160
44
P MYC008 Myocarditis 56 0.159
45
PRP080 Peripheral Artery Disease 35 0.157
46
P AST005 Asthma 80 0.157
47
c CRN173 Coronary Heart Disease 8 19 0.157
48
MSC004 Muscle Tissue Disease 35 0.154
49
RSP006 Respiratory System Disease 61 0.153
50
ATH003 Atherosclerosis 63 0.153
51
P OBS005 Obesity 91 0.153
52
PRP019 Peripheral Nervous System Disease 52 0.150
53
ATN002 Autonomic Nervous System Disease 46 0.149
54
P BRS047 Breast Cancer 100 0.148
55
P PLM037 Pulmonary Hypertension 78 0.147
56
P RSP003 Respiratory Failure 68 0.147
57
BCK006 Back Pain 40 0.145
58
P ART023 Arthropathy 63 0.142
59
P HPT021 Hepatitis 74 0.139
60
P MSC033 Muscle Disorders 52 0.138
61
NRN002 Neuronitis 40 0.137
62
STR067 Stroke, Ischemic 74 0.136
63
SYN036 Syncope 45 0.135
64
UNV002 Univentricular Heart 24 0.134
65
RHM001 Rheumatic Fever 50 0.132
66
RHM027 Rheumatic Disease 55 0.131
67
c CRN177 Coronary Heart Disease 7 21 0.131
68
P END033 Endocarditis 52 0.131
69
P CHR345 Chronic Pain 45 0.130
70
SLP005 Sleep Disorder 52 0.130
71
P SLP006 Sleep Apnea 60 0.130
72
NRM005 Neuromuscular Disease 56 0.129
73
ANR040 Aneurysm 56 0.129
74
P HYP061 Hypertrophic Cardiomyopathy 64 0.126
75
P VNT002 Ventricular Septal Defect 59 0.125
76
CNN005 Connective Tissue Disease 60 0.125
77
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.124
78
P KDN018 Kidney Disease 64 0.124
79
SDD007 Sudden Cardiac Death 46 0.123
80
HRT007 Heart Cancer 51 0.122
81
HV1006 Hiv-1 80 0.122
82
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.122
83
HYP266 Hypoxia 55 0.122
84
P THY032 Thyroiditis 57 0.122
85
ART017 Aortic Disease 57 0.122
86
c HYP595 Hypertension, Essential 69 0.121
87
c FML001 Familial Atrial Fibrillation 59 0.120
88
INF013 Inferior Myocardial Infarction 36 0.120
89
P SCK002 Sick Sinus Syndrome 49 0.119
90
JNT002 Joint Disorders 55 0.119
91
c AST037 Asthma 1 35 0.119
92
IMP003 Impaired Renal Function Disease 36 0.118
93
P LPS004 Lupus Erythematosus 63 0.118
94
c MYC058 Myocardial Infarction 2 28 0.117
95
PRS047 Prostatitis 56 0.117
96
VND001 Vein Disease 51 0.117
97
P HYP086 Hypothyroidism 63 0.116
98
P CLL015 Collagen Disease 49 0.116
99
P HRT017 Heart Tumor 34 0.115
100
P LYM118 Lymphoma 68 0.115
101
BRT030 Birth Defects 44 0.114
102
c AST039 Asthma 2 28 0.114
103
P LKM002 Leukemia 70 0.114
104
c CHR089 Chronic Kidney Failure 67 0.113
105
P NRV006 Nervous System Cancer 62 0.113
106
MVM001 Movement Disease 45 0.113
107
LNG099 Lung Disease 63 0.113
108
BNF002 Bone Fracture 46 0.112
109
ANG054 Angina Pectoris 48 0.111
110
P LNG028 Long Qt Syndrome 67 0.111
111
P RHM011 Rheumatoid Arthritis 87 0.110
112
c ADL079 Adult Heart Tumor 17 0.109
113
ACR041 Acromelic Frontonasal Dysostosis 45 0.108
114
PHY002 Physical Disorder 43 0.108
115
CRB039 Cerebrovascular Disease 49 0.108
116
ATN005 Autonomic Dysfunction 44 0.107
117
P OST012 Osteoarthritis 81 0.107
118
c CRN176 Coronary Heart Disease 9 19 0.106
119
NTR005 Nutritional Deficiency Disease 51 0.106
120
ANX002 Anxiety Disorder 67 0.105
121
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 57 0.105
122
PRP021 Peripheral Nervous System Neoplasm 49 0.105
123
P PNC044 Pancreatitis 62 0.104
124
CRD119 Cardiac Arrest 63 0.104
125
PLP001 Pulpitis 45 0.104
126
CRN030 Coronary Stenosis 50 0.104
127
c CHR096 Chronic Pulmonary Heart Disease 40 0.104
128
FRS012 First-Degree Atrioventricular Block 29 0.103
129
END030 End Stage Renal Failure 53 0.103
130
c CLD010 Cold-Induced Sweating Syndrome 1 43 0.103
131
P SPS003 Spastic Diplegia 49 0.103
132
THR099 Third-Degree Atrioventricular Block 31 0.102
133
TTR001 Tetralogy of Fallot 69 0.102
134
HDC001 Headache 52 0.102
135
CRB009 Cerebritis 36 0.102
136
CRT057 Critical Congenital Heart Disease 19 0.102
137
ALR002 Al-Raqad Syndrome 36 0.101
138
CRB031 Cerebral Arterial Disease 31 0.101
139
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 59 0.101
140
PRD011 Proud Syndrome 42 0.101
141
PCK002 Pick Disease 66 0.100
142
c SYS001 Systemic Lupus Erythematosus 87 0.100
143
DXT001 Dextrocardia 44 0.100
144
GLC008 Glucose Metabolism Disease 44 0.100
145
LRN003 Learning Disability 49 0.099
146
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 45 0.099
147
SNS023 Sensory System Cancer 45 0.098
148
AYM001 Ayme-Gripp Syndrome 40 0.098
149
P MSC005 Muscular Dystrophy 64 0.098
150
P PRS040 Prostate Cancer 89 0.097
151
CRD003 Cardiac Sarcoidosis 39 0.096
152
P LNG032 Lung Cancer 92 0.096
153
INF034 Infective Endocarditis 50 0.096
154
BLD053 Blood Platelet Disease 44 0.095
155
c ACT076 Acute Myocarditis 40 0.095
156
P ENC018 Encephalopathy 59 0.095
157
P ACT080 Acute Pulmonary Heart Disease 31 0.095
158
GNR004 Generalized Anxiety Disorder 49 0.094
159
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 35 0.094
160
P MYL007 Myeloma 52 0.094
161
MNT002 Mental Depression 52 0.093
162
VNT011 Ventricular Fibrillation, Familial, 1 35 0.093
163
TRN044 Transposition of the Great Arteries 48 0.093
164
c ACT071 Acute Kidney Failure 48 0.092
165
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 40 0.092
166
ALN001 Aland Island Eye Disease 45 0.092
167
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.092
168
VSC047 Vascular Malformation 45 0.092
169
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.092
170
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 41 0.091
171
P MTR012 Mitral Valve Disease 59 0.091
172
CRB004 Cerebral Artery Occlusion 39 0.091
173
END040 Endogenous Depression 51 0.091
174
MLN008 Melanoma 61 0.090
175
P INF032 Infertility 61 0.090
176
WLF001 Wolff-Parkinson-White Syndrome 58 0.090
177
P CRD132 Cardiac Conduction Defect 35 0.090
178
SPN041 Spinal Cord Disease 50 0.090
179
c BLD124 Bleeding Disorder, Platelet-Type, 11 37 0.090
180
c TRC078 Trichohepatoenteric Syndrome 2 30 0.089
181
ADJ001 Adjustment Disorder 38 0.089
182
PLM033 Pulmonary Embolism 59 0.088
183
P BRG001 Brugada Syndrome 59 0.088
184
SRC014 Sarcoma 66 0.088
185
OBS061 Obstructive Sleep Apnea 61 0.088
186
ALL026 Allergic Hypersensitivity Disease 53 0.088
187
P CRV039 Cervicitis 45 0.087
188
P RST002 Restrictive Cardiomyopathy 48 0.087
189
LPD008 Lipid Metabolism Disorder 42 0.086
190
P PNM007 Pneumonia 67 0.086
191
MTH009 Mouth Disease 63 0.086
192
c ART101 Aortic Valve Disease 2 56 0.086
193
CHL071 Child Syndrome 58 0.085
194
P ADN016 Adenocarcinoma 69 0.085
195
CND002 Conduct Disorder 54 0.085
196
RNL097 Renal Artery Disease 44 0.085
197
CSY001 C Syndrome 49 0.084
198
KRN002 Kearns-Sayre Syndrome 60 0.084
199
P NRV007 Nervous System Disease 71 0.084
200
P DYS021 Dysautonomia 47 0.084
201
HPT023 Hepatocellular Carcinoma 90 0.084
202
HRT008 Heart Conduction Disease 43 0.084
203
LPD004 Lipoid Nephrosis 49 0.084
204
KDS001 Kid Syndrome 53 0.084
205
P AMY004 Amyloidosis 63 0.084
206
P INF038 Influenza 71 0.083
207
END020 Endocardial Fibroelastosis 44 0.083
208
ATN004 Autonomic Neuropathy 44 0.082
209
PLM129 Pulmonary Disease, Chronic Obstructive 61 0.082
210
MSC072 Muscle Cancer 47 0.082
211
MVD001 Moved to 60 0.082
212
P PLM040 Pulmonary Valve Disease 45 0.081
213
PRN021 Paranasal Sinus Disease 50 0.081
214
NSL022 Nasal Cavity Disease 41 0.081
215
INT007 Intermediate Coronary Syndrome 52 0.081
216
c MLT019 Multiple Myeloma 77 0.081
217
GDS001 Good Syndrome 46 0.080
218
ING001 Inguinal Hernia 57 0.080
219
BRN080 Brain Ischemia 42 0.080
220
WTH001 Withdrawal Disorder 36 0.080
221
CMP010 Complex Regional Pain Syndrome 59 0.080
222
P LVR013 Liver Disease 76 0.080
223
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 34 0.080
224
PLM010 Pulmonary Edema 56 0.080
225
TTH006 Tooth Disease 52 0.080
226
DPH021 Diaphragm Disease 45 0.079
227
WLL006 Wells Syndrome 57 0.079
228
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.079
229
CRD137 Cardiogenic Shock 44 0.079
230
c CNG031 Congenital Nervous System Abnormality 39 0.078
231
CHG001 Chagas Disease 62 0.078
232
INS024 Insulin-Like Growth Factor I 75 0.077
233
CRT016 Carotid Artery Disease 54 0.076
234
P HYP071 Hypersensitivity Reaction Type Ii Disease 46 0.076
235
P URF003 Urofacial Syndrome 1 51 0.076
236
HYP540 Hypertension, Diastolic 40 0.075
237
c HPT001 Hepatitis C 68 0.075
238
MLR004 Malaria 80 0.075
239
P LFT003 Left Ventricular Noncompaction 48 0.074
240
CRN017 Coronary Thrombosis 46 0.074
241
BNS002 Bone Structure Disease 37 0.074
242
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 27 0.074
243
EXF001 Exfoliation Syndrome 56 0.073
244
P EPL164 Epilepsy 60 0.073
245
URN009 Urinary System Disease 52 0.073
246
c VNT013 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1 46 0.072
247
SPC003 Specific Developmental Disorder 39 0.072
248
HYP005 Hypokalemia 52 0.072
249
P PLN008 Peeling Skin Syndrome 45 0.072
250
P RNL015 Renal Hypertension 47 0.072
251
MYX004 Myxedema 36 0.072
252
PRC013 Pericarditis 52 0.071
253
c MTR002 Mitral Valve Insufficiency 42 0.071
254
c CNT035 Central Nervous System Disease 60 0.071
255
MDS022 Mediastinitis 37 0.071
256
ART016 Aortic Aneurysm 67 0.071
257
PRC012 Pericardial Effusion 50 0.071
258
CRD001 Cardiac Tamponade 43 0.071
259
TBR010 Tuberculosis 70 0.071
260
P NNT042 Neonatal Lupus Erythematosus 34 0.071
261
BLD054 Blood Protein Disease 38 0.070
262
P LFR001 Li-Fraumeni Syndrome 79 0.070
263
P HLT001 Holt-Oram Syndrome 60 0.070
264
P MYT002 Myotonic Dystrophy 46 0.070
265
MDY003 Mody, Type Ii 36 0.070
266
HTR003 Heterotaxy 41 0.069
267
P PLY019 Polyneuropathy 53 0.069
268
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 21 0.069
269
P CLR023 Colorectal Cancer 96 0.069
270
P HRP006 Herpes Simplex 65 0.069
271
PRP009 Peripartum Cardiomyopathy 41 0.069
272
BRS051 Breast Disease 57 0.069
273
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 56 0.069
274
BRN071 Brain Injury 51 0.069
275
P MSC007 Muscle Hypertrophy 55 0.069
276
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 55 0.068
277
TRC062 Tricuspid Atresia 34 0.068
278
c HPT073 Hepatitis C Virus 72 0.068
279
VSC009 Vascular Skin Disease 21 0.068
280
RDN001 Reading Disorder 39 0.067
281
P ATR010 Atrial Heart Septal Defect 41 0.067
282
CRT015 Carotid Artery Occlusion 43 0.067
283
FML039 Female Reproductive System Disease 49 0.067
284
P CTR002 Cataract 57 0.067
285
c ATM022 Autoimmune Myocarditis 39 0.067
286
ANX004 Anoxia 45 0.067
287
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.067
288
THY030 Thyroid Gland Disease 52 0.066
289
GNT019 Giant Cell Myocarditis 31 0.066
290
RPR002 Reproductive System Disease 45 0.066
291
ATR024 Atrial Fibrillation and Stroke 19 0.066
292
ADL002 Adult Syndrome 53 0.066
293
VSC008 Vascular Hemostatic Disease 30 0.066
294
DFC004 Deficiency Anemia 64 0.066
295
c ART115 Aortic Valve Disease 1 53 0.066
296
P PHC003 Pheochromocytoma 72 0.065
297
P HYP076 Hyperthyroidism 59 0.065
298
HYP066 Hyperglycemia 61 0.065
299
PNM008 Pneumothorax 51 0.065
300
MYC005 Myocardial Stunning 44 0.065
301
CTS003 Coats Disease 57 0.065
302
FBR012 Fabry Disease 68 0.064
303
STS002 Situs Inversus 43 0.064
304
c OST147 Osteoarthritis 1 31 0.064
305
P SHR029 Short Syndrome 60 0.064
306
P THR014 Thrombocytopenia 63 0.064
307
c DYS033 Dysautonomia Like Disorder 18 0.064
308
PRT036 Peritonitis 65 0.064
309
LFT009 Left Ventricular Outflow Tract Obstruction 43 0.064
310
BRN028 Brain Cancer 69 0.063
311
MYC002 Mycobacterium Avium Complex Disease 52 0.063
312
P INT070 Intestinal Obstruction 55 0.063
313
ISC005 Ischemic Bone Disease 38 0.063
314
P PRD008 Periodontitis 46 0.063
315
CNG134 Congenitally Corrected Transposition of the Great Arteries 25 0.063
316
UPP004 Upper Respiratory Tract Disease 48 0.063
317
PNC034 Pancreas Disease 56 0.063
318
P OVR042 Ovarian Cancer 73 0.062
319
OVR063 Overnutrition 49 0.062
320
P FML035 Familial Hyperlipidemia 49 0.062
321
PST053 Postherpetic Neuralgia 41 0.062
322
c THR092 Thrombophilia Due to Thrombin Defect 56 0.062
323
P NRB001 Neuroblastoma 70 0.062
324
PST028 Post-Traumatic Stress Disorder 55 0.062
325
ALL006 Allergic Asthma 59 0.062
326
WST001 West Syndrome 61 0.062
327
EBS001 Ebstein Anomaly 44 0.062
328
GST053 Gastric Cancer 52 0.061
329
PLM041 Pulmonary Valve Stenosis 48 0.061
330
P DBT005 Diabetes Insipidus 53 0.061
331
CRB025 Carbohydrate Metabolic Disorder 46 0.061
332
HRT011 Heart Septal Defect 40 0.061
333
SKN023 Skin Tag 48 0.061
334
DSS008 Disease of Mental Health 48 0.061
335
SNS003 Sensory Peripheral Neuropathy 44 0.061
336
PLC008 Placenta Disease 33 0.061
337
BLD044 Bladder Disease 50 0.061
338
c MCR129 Microvascular Complications of Diabetes 1 55 0.061
339
RTN023 Retinitis 49 0.061
340
SPN051 Spondylitis 50 0.061
341
VSC006 Vascular Cancer 51 0.061
342
BRS090 Breast Reconstruction 38 0.060
343
CYT008 Cytomegalovirus Infection 51 0.060
344
SKN016 Skin Disease 69 0.060
345
ART005 Arteriovenous Malformation 63 0.060
346
DBT002 Diabetic Autonomic Neuropathy 37 0.060
347
P BLD051 Blood Coagulation Disease 44 0.059
348
ACD009 Acid-Labile Subunit, Deficiency of 37 0.059
349
c PST001 Posterior Myocardial Infarction 32 0.059
350
DWN001 Down Syndrome 65 0.059
351
FCL011 Facial Nerve Disease 37 0.059
352
PRP050 Peripheral Arterial Occlusive Disease 1 16 0.059
353
CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 42 0.059
354
MNN017 Mononeuropathy 37 0.059
355
PTN001 Patent Foramen Ovale 55 0.059
356
CRB087 Cerebral Arteriosclerosis 23 0.059
357
VSC011 Vasculitis 62 0.058
358
CRT028 Cor Triatriatum 22 0.058
359
ETN001 Eating Disorder 59 0.058
360
c RNL016 Renal Infectious Disease 22 0.058
361
PRS036 Parasitic Protozoa Infectious Disease 45 0.058
362
PLY023 Polycystic Liver Disease 57 0.058
363
c HPT016 Hepatitis B 61 0.058
364
c PLN018 Peeling Skin Syndrome 2 36 0.058
365
P EXN002 Exanthem 57 0.058
366
P INT143 Interstitial Cystitis 57 0.057
367
P TRC086 Trichohepatoenteric Syndrome 1 46 0.057
368
c PLM128 Pulmonary Hypertension, Primary, 2 36 0.057
369
CPL005 Capillary Disease 39 0.057
370
NSD001 Nose Disease 51 0.057
371
P INT068 Intestinal Disease 60 0.057
372
c PNC106 Pancreatic Agenesis 1 31 0.057
373
c PLM022 Pulmonary Valve Insufficiency 37 0.057
374
BRC012 Brucellosis 66 0.056
375
HYD012 Hydrops Fetalis 45 0.056
376
CHN016 Cohen Syndrome 55 0.056
377
MLR007 Male Reproductive System Disease 36 0.056
378
P LRY019 Laryngitis 55 0.056
379
SXD001 Sex Differentiation Disease 39 0.056
380
SNT005 Sinoatrial Node Disease 34 0.056
381
GLT021 Glutaricaciduria, Type I 47 0.056
382
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 28 0.056
383
SPS057 Spasticity 41 0.056
384
GNC005 Geniculate Ganglionitis 27 0.056
385
BRN106 Burns 52 0.055
386
P MSC003 Muscular Atrophy 51 0.055
387
ATR055 Atrial Septal Aneurysm 23 0.055
388
P HYP040 Hypospadias 58 0.055
389
HYP056 Hypoglycemia 60 0.055
390
P SKN013 Skin Benign Neoplasm 38 0.055
391
ATM052 Autoimmune Disease 1 26 0.054
392
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 34 0.054
393
MTR007 Motor Peripheral Neuropathy 44 0.054
394
P HYP265 Hypotonia 39 0.054
395
P ANR007 Anorexia Nervosa 63 0.054
396
ART012 Aortitis 32 0.054
397
c SBC003 Subacute Bacterial Endocarditis 33 0.054
398
P PLY006 Polydactyly 56 0.054
399
P ATR001 Atrioventricular Septal Defect 52 0.054
400
CCN007 Cocoon Syndrome 32 0.054
401
GNG013 Gingivitis 61 0.054
402
HPT074 Hepatic Adenoma, Somatic 35 0.054
403
MXD005 Mixed Connective Tissue Disease 63 0.053
404
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.053
405
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 42 0.053
406
SPN186 Spinal Cord Injury 62 0.053
407
URT001 Urethritis 39 0.053
408
WLS001 Wilson Disease 72 0.053
409
BCK001 Becker Muscular Dystrophy 68 0.053
410
GST050 Gastrointestinal System Disease 58 0.053
411
C3D001 C3 Deficiency 50 0.053
412
P PRX010 Paroxysmal Ventricular Fibrillation 33 0.053
413
c ACT210 Acute Respiratory Distress Syndrome 55 0.053
414
HDN002 Head Injury 47 0.053
415
SXL003 Sexual Disorder 45 0.053
416
NSY001 N Syndrome 42 0.053
417
ALC010 Alcoholic Cardiomyopathy 38 0.053
418
CRB085 Cerebral Hemorrhage 40 0.053
419
HRT029 Heart Tumor of the Child 16 0.053
420
MGR028 Migraine with or Without Aura 1 49 0.053
421
ATN003 Autonomic Nervous System Neoplasm 43 0.053
422
PRS042 Prostate Disease 50 0.053
423
PHR003 Pharyngitis 58 0.053
424
P TRC087 Tricuspid Valve Disease 41 0.053
425
P PLM036 Pulmonary Fibrosis 69 0.053
426
P VNS003 Venous Insufficiency 53 0.053
427
SML033 Small Cell Cancer of the Lung, Somatic 53 0.052
428
c PLN021 Peeling Skin Syndrome 3 30 0.052
429
BRN055 Bronchogenic Cyst 27 0.052
430
CNV002 Conversion Disorder 45 0.052
431
P EMR001 Emery-Dreifuss Muscular Dystrophy 57 0.052
432
P ARC016 Auriculocondylar Syndrome 1 44 0.052
433
PRD007 Periodontal Disease 42 0.052
434
SNT004 Sinoatrial Node Dysfunction and Deafness 25 0.052
435
HRT006 Heart Aneurysm 27 0.052
436
DMN002 Dementia 62 0.052
437
P HMN010 Hemangioma 62 0.052
438
P ESP024 Esophagitis 62 0.052
439
ADR005 Adrenal Carcinoma 57 0.052
440
RFL001 Reflex Sympathetic Dystrophy 45 0.052
441
GLB001 Gilbert Syndrome 59 0.052
442
ACT084 Acute Stress Disorder 38 0.052
443
BRN002 Bronchiolitis 56 0.052
444
PRM025 Primary Bacterial Infectious Disease 42 0.051
445
P SYS005 Systemic Scleroderma 60 0.051
446
PRN037 Prinzmetal's Variant Angina 30 0.051
447
CRB008 Cerebral Atherosclerosis 37 0.051
448
ADR038 Adermatoglyphia 39 0.051
449
CRB037 Cerebral Palsy 54 0.051
450
P ART084 Arteriovenous Fistula 40 0.051
451
P MMB011 Membranous Nephropathy 53 0.051
452
STM006 Stomach Disease 48 0.051
453
PLS007 Plasmodium Falciparum Malaria 56 0.051
454
CNS004 Constipation 57 0.051
455
P MYL006 Myeloid Leukemia 67 0.051
456
P GLL020 Gallbladder Disease 59 0.050
457
CLT003 Colitis 56 0.050
458
ATM053 Autoimmune Disease 2 16 0.050
459
ANG049 Angioedema Induced by Ace Inhibitors 35 0.050
460
CYS001 Cystic Fibrosis 87 0.050
461
LYM017 Lyme Disease 64 0.050
462
c PLN017 Peeling Skin Syndrome 1 32 0.050
463
P CLC005 Celiac Disease 67 0.050
464
P GLM007 Glomerulonephritis 56 0.050
465
BRN024 Bronchitis 67 0.050
466
CHL123 Chlamydia 60 0.050
467
PTN002 Patent Ductus Arteriosus 50 0.049
468
P PLY011 Polycystic Ovary Syndrome 64 0.049
469
P ADL010 Adult Respiratory Distress Syndrome 60 0.049
470
SKN027 Skin Conditions 44 0.049
471
SCK005 Sickle Cell Disease 51 0.049
472
HMS001 Hemosiderosis 42 0.049
473
HRP004 Herpes Zoster 56 0.049
474
P RHN004 Rhinitis 59 0.049
475
ATN001 Autonomic Peripheral Neuropathy 19 0.049
476
SPT001 Septal Myocardial Infarction 16 0.049
477
CLC007 Calcium Metabolism Disease 39 0.049
478
ADT003 Auditory System Disease 49 0.049
479
P CNJ013 Conjunctivitis 65 0.049
480
P MNN013 Meningitis 66 0.049
481
PHC013 Phaeochromocytoma 47 0.049
482
c SVR001 Severe Acute Respiratory Syndrome 56 0.049
483
CHL067 Cholecystitis 57 0.048
484
P GRV001 Graves' Disease 62 0.048
485
P STM004 Stomach Cancer 73 0.048
486
DBT010 Diabetic Neuropathy 55 0.048
487
P SCH015 Schizophrenia 78 0.048
488
VHW001 Vohwinkel Syndrome 47 0.048
489
NRR001 Neuroretinitis 41 0.048
490
OTP003 Oto-Palatal-Digital Syndrome 14 0.048
491
RNL001 Renal Artery Obstruction 31 0.048
492
HTR014 Heterotaxy, Visceral, 1, X-Linked 31 0.048
493
CRD016 Cardiac Rupture 32 0.048
494
LMB062 Limb Ischemia 48 0.048
495
c CRD099 Cardiomyopathy, Dilated, 1e 42 0.048
496
FML037 Female Breast Cancer 49 0.048
497
ADR009 Adrenal Cortex Disease 40 0.047
498
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.047
499
SCK003 Sickle Cell Anemia 72 0.047
500
ACT017 Acute Chest Syndrome 50 0.047
501
PRP030 Purpura 60 0.047
502
PLM001 Pulmonary Tuberculosis 69 0.047
503
c SHR030 Short Qt Syndrome 45 0.047
504
ACT094 Acute Articular Rheumatism 20 0.047
505
P SDD001 Sudden Infant Death Syndrome 60 0.047
506
RGH009 Right Atrial Isomerism 31 0.047
507
P ATX004 Ataxia 53 0.047
508
GNR003 Generalized Atherosclerosis 35 0.047
509
RHB003 Rhabdomyosarcoma 55 0.047
510
P CHR071 Charcot-Marie-Tooth Disease 66 0.047
511
PRT055 Prieto X-Linked Mental Retardation Syndrome 24 0.047
512
PLY039 Polymorphic Reticulosis 20 0.047
513
THY028 Thyroid Cancer 71 0.047
514
P MYS003 Myasthenia Gravis 64 0.047
515
ATM054 Autoimmune Disease 3 16 0.047
516
END038 Endocrine Pancreas Disease 42 0.047
517
ETH011 Ethylmalonic Encephalopathy 57 0.047
518
P BCL006 B-Cell Lymphomas 64 0.047
519
GLC003 Glucose Intolerance 56 0.047
520
SPR035 Superior Vena Cava Syndrome 31 0.047
521
ACR007 Acromegaly 66 0.046
522
P ASP006 Aspergillosis 61 0.046
523
INT066 Interstitial Lung Disease 60 0.046
524
c SCK017 Sick Sinus Syndrome 1 32 0.046
525
GYN001 Gynecomastia 49 0.046
526
ATM005 Autoimmune Disease of Musculoskeletal System 14 0.046
527
HSB001 His Bundle Tachycardia 21 0.046
528
ATM013 Autoimmune Disease of Cardiovascular System 14 0.046
529
P NPH009 Nephrolithiasis 59 0.046
530
P UTR038 Uterine Disease 38 0.046
531
P ALX003 Alexander Disease 64 0.046
532
TNP003 Tn Polyagglutination Syndrome, Somatic 30 0.046
533
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 21 0.046
534
P ANT006 Antiphospholipid Syndrome 60 0.045
535
DXT002 Dextrocardia with Situs Inversus 34 0.045
536
GST023 Gastric Ulcer 56 0.045
537
c CHR431 Chronic Venous Insufficiency 43 0.045
538
SBC016 Subacute Delirium 23 0.045
539
MYT011 Myotonia 40 0.045
540
TRC026 Tracheal Disease 33 0.045
541
P SZR006 Seizure Disorder 56 0.045
542
DRM006 Dermatitis 58 0.045
543
ATP002 Atopy 62 0.045
544
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 42 0.045
545
P SPN052 Spondyloarthropathy 58 0.045
546
P NRP037 Neuropathy, Hereditary Sensory and Autonomic, Type V 53 0.045
547
PLS006 Plasmodium Vivax Malaria 52 0.045
548
c ART106 Arterial Calcification, Generalized, of Infancy, 1 32 0.045
549
DRG001 Drug Psychosis 39 0.045
550
PRG004 Progeria 54 0.044
551
WLL001 Williams-Beuren Syndrome 61 0.044
552
P THL005 Thalassemia 61 0.044
553
HMP001 Hemopericardium 32 0.044
554
c TRC022 Tricuspid Valve Insufficiency 33 0.044
555
P CRN074 Coronary Artery Aneurysm 44 0.044
556
P HNT016 Huntington Disease 80 0.044
557
P KDN017 Kidney Cancer 67 0.044
558
P SPN046 Spinal Muscular Atrophy 62 0.044
559
BRN012 Bronchiolitis Obliterans 58 0.044
560
DXR001 Doxorubicin Induced Cardiomyopathy 36 0.044
561
PST055 Postural Hypotension 36 0.044
562
c BRG005 Brugada Syndrome 1 42 0.044
563
c HPT003 Hepatitis a 55 0.044
564
P PRT013 Portal Hypertension 61 0.044
565
INT040 Intrinsic Asthma 40 0.044
566
GRB002 Gerbode Defect 16 0.044
567
RHM029 Rheumatic Fever-Related Antigen Rheumatic Fever, Acute, Susceptibility to, Included 24 0.044
568
c ACT134 Acute Liver Failure 46 0.044
569
P LPS002 Liposarcoma 50 0.044
570
P RNL014 Renal Cell Carcinoma 80 0.043
571
GLB003 Globe Disease 34 0.043
572
TTN003 Tetanus 62 0.043
573
RNL077 Renal Fibrosis 48 0.043
574
DCB001 Decubitus Ulcer 44 0.043
575
P ENC004 Encephalitis 60 0.043
576
c OST112 Osteoarthritis-5 38 0.043
577
CLS010 Cluster Headache 43 0.043
578
P ADD001 Addison's Disease 60 0.043
579
QDR001 Quadriplegia 51 0.043
580
MLR006 Male Reproductive Organ Cancer 46 0.043
581
END035 Endocrine Gland Cancer 50 0.043
582
P SML001 Small Cell Carcinoma 54 0.043
583
STM007 Stomatitis 50 0.043
584
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 32 0.043
585
DCH001 Duchenne Muscular Dystrophy 81 0.043
586
P TMT001 Timothy Syndrome 58 0.043
587
OLV001 Olivopontocerebellar Atrophy 53 0.043
588
P LMY004 Leiomyosarcoma 54 0.043
589
FNT004 Fainting 33 0.042
590
PRT037 Pertussis 63 0.042
591
PSR001 Psoriatic Arthritis 64 0.042
592
P ERY008 Erythromelalgia 50 0.042
593
MRB003 Morbid Obesity 59 0.042
594
GND003 Gonadal Disease 41 0.042
595
ACT174 Acute Peripheral Arterial Occlusion 16 0.042
596
P PLM085 Pulmonary Hemosiderosis 45 0.042
597
P ABD003 Abdominal Aortic Aneurysm 43 0.042
598
P HYP065 Hyperaldosteronism 52 0.042
599
PRS045 Prostatic Hypertrophy 44 0.042
600
CRT013 Carotid Stenosis 35 0.042
601
LVC002 Levocardia 19 0.042
602
OCY001 Oocyte Maturation Defect 31 0.042
603
PSY004 Psychotic Disorder 62 0.042
604
P OST002 Osteoporosis 63 0.042
605
LVR012 Liver Cirrhosis 71 0.042
606
INC022 Inclusion-Cell Disease 46 0.042
607
FTT001 Fatty Liver Disease 60 0.042
608
IRN002 Iron Metabolism Disease 38 0.042
609
CLV009 Clove Syndrome, Somatic 41 0.042
610
BRN038 Bronchial Disease 54 0.042
611
INT002 Intermittent Claudication 56 0.042
612
CLC006 Calcinosis 48 0.042
613
PLM034 Pulmonary Emphysema 55 0.042
614
PST048 Postural Orthostatic Tachycardia Syndrome 29 0.042
615
CLF001 Cleft Lip 48 0.042
616
c LNG044 Long Qt Syndrome 1 59 0.041
617
ACH005 Achalasia 55 0.041
618
c CNG006 Congenital Hypothyroidism 59 0.041
619
ESP023 Esophageal Disease 52 0.041
620
DPH001 Diphtheria 55 0.041
621
P PLY041 Polymyositis 49 0.041
622
GST078 Gastrointestinal Allergy 41 0.041
623
P MYM002 Moyamoya Disease 60 0.041
624
ACH001 Acheiropody 47 0.041
625
P HRD018 Hair Disease 48 0.041
626
BLR006 Biliary Tract Disease 50 0.041
627
ALG001 Algoneurodystrophy 34 0.041
628
VCC001 Vaccinia 46 0.041
629
FRZ001 Frozen Shoulder 40 0.041
630
OCC004 Occlusion of Gallbladder 15 0.041
631
EPD019 Epidural Neoplasm 34 0.041
632
ANT005 Anteroseptal Myocardial Infarction 23 0.041
633
PNC065 Pinched Nerve 11 0.041
634
P TRC005 Tracheal Stenosis 36 0.041
635
END074 Endocardium Disease 26 0.041
636
PLS010 Plasma Protein Metabolism Disease 37 0.041
637
PRP016 Paraplegia 49 0.041
638
GST045 Gastroenteritis 59 0.041
639
P ALC004 Alcohol Abuse 57 0.041
640
DRG003 Drug Dependence 53 0.041
641
PRP028 Peripheral Vertigo 42 0.041
642
P GNR027 Generalized Peeling Skin Syndrome 21 0.041
643
CRC034 Carcinoma Showing Thymus-Like Differentiation 21 0.041
644
ACR002 Acrocapitofemoral Dysplasia 35 0.040
645
OCL006 Ocular Hypertension 47 0.040
646
BND014 Bone Development Disease 40 0.040
647
RSS002 Roussy-Levy Syndrome 51 0.040
648
ADR016 Adrenal Cortical Carcinoma 60 0.040
649
ATM059 Autoimmune Disease 6 23 0.040
650
FBR054 Fibroma 44 0.040
651
HND003 Hand-Foot-Uterus Syndrome 46 0.040
652
P DMY001 Demyelinating Polyneuropathy 41 0.040
653
TRC021 Tricuspid Valve Stenosis 37 0.040
654
MTB004 Metabolic Acidosis 49 0.040
655
c HYP073 Hypersensitivity Reaction Type Iv Disease 45 0.040
656
c SPN225 Spondyloarthropathy 1 62 0.039
657
P OCL013 Oculodentodigital Dysplasia 58 0.039
658
RLP001 Relapsing Polychondritis 52 0.039
659
ATM014 Autoimmune Disease of Endocrine System 37 0.039
660
P CSH001 Cushing's Syndrome 65 0.039
661
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.039
662
PRM042 Primary Effusion Lymphoma 55 0.039
663
ANK001 Ankylosis 52 0.039
664
CRB086 Cerebral Aneurysms 39 0.039
665
HDG012 Hodgkin Lymphoma 75 0.039
666
c MYT021 Myotonic Dystrophy 1 64 0.039
667
P PTS002 Ptosis 56 0.039
668
SPT004 Septic Arthritis 60 0.039
669
TNS005 Tonsillitis 58 0.039
670
WRN001 Werner Syndrome 69 0.039
671
P TRN020 Turner Syndrome 64 0.039
672
HPR003 Heparin-Induced Thrombocytopenia 45 0.039
673
PLM068 Pulmonary Vein Stenosis 39 0.039
674
c CHR095 Chronic Progressive External Ophthalmoplegia 48 0.038
675
MSL001 Measles 61 0.038
676
P END044 Endometriosis 53 0.038
677
NRV004 Nerve Compression Syndrome 33 0.038
678
FMR003 Femoral Neuropathy 34 0.038
679
ADR012 Adrenal Gland Disease 49 0.038
680
CLN019 Colonic Disease 50 0.038
681
P CHR102 Charcot-Marie-Tooth Neuropathy 43 0.038
682
ATM055 Autoimmune Disease 4 16 0.038
683
P JRV003 Jervell and Lange-Nielsen Syndrome 53 0.038
684
P MCR113 Microvascular Complications of Diabetes 3 48 0.038
685
BLR001 Biliary Atresia 52 0.038
686
P CYS018 Cystitis 54 0.038
687
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.038
688
c INF067 Inflammatory Bowel Disease 10 31 0.038
689
CHL004 Cholelithiasis 48 0.038
690
c CNG148 Congenital Heart Disease, Atrial Septal Defect 17 0.038
691
RBR001 Roberts Syndrome 61 0.038
692
CHR103 Charge Syndrome 64 0.038
693
TXC005 Toxic Shock Syndrome 61 0.038
694
P CHN005 Choanal Atresia 42 0.038
695
PMS001 Poems Syndrome 56 0.038
696
MRC001 Marchiafava Bignami Disease 33 0.038
697
FCT008 Factitious Disorder 42 0.038
698
ART008 Arteriosclerosis Obliterans 41 0.038
699
CRN006 Coronary Aneurysm 31 0.038
700
ATM012 Autoimmune Disease of Blood 36 0.038
701
P LMB006 Limb-Girdle Muscular Dystrophy 54 0.038
702
HYP020 Hyperprolactinemia 58 0.038
703
GNG011 Gingival Disease 50 0.038
704
CNT017 Central Nervous System Origin Vertigo 27 0.038
705
P MTC004 Mitochondrial Encephalomyopathy 39 0.038
706
NRT004 Neuritis 52 0.038
707
P ENC011 Encephalomyopathy 35 0.038
708
MLT131 Multifocal Atrial Tachycardia 14 0.038
709
c CLL013 Cell Type Cancer 46 0.038
710
P DYS154 Dystonia 62 0.038
711
ALC007 Alcohol Dependence 66 0.038
712
P PLR004 Pleuropulmonary Blastoma 63 0.038
713
APP015 Apparent Mineralocorticoid Excess 50 0.038
714
c ATM003 Autoimmune Thyroiditis 59 0.038
715
APP008 Appendicitis 61 0.038
716
P SNS014 Sinusitis 66 0.038
717
P CMP008 Compartment Syndrome 46 0.038
718
TMP001 Temporal Lobe Epilepsy 47 0.038
719
LWN001 Lown-Ganong-Levine Syndrome 28 0.038
720
HYP043 Hyperandrogenism 46 0.038
721
HYL004 Hyaline Fibromatosis Syndrome 38 0.037
722
P HMC002 Homocystinuria 52 0.037
723
P PSR002 Psoriasis 63 0.037
724
TRN015 Transient Cerebral Ischemia 57 0.037
725
P HYP083 Hypopituitarism 50 0.037
726
INT075 Intracranial Hypertension 52 0.037
727
DBL004 Double Discordia 9 0.037
728
P ESN007 Eosinophilia 61 0.037
729
c VNT028 Ventricular Septal Defect 1 30 0.037
730
P PLY014 Polycystic Kidney Disease 60 0.037
731
VTM003 Vitamin Metabolic Disorder 31 0.037
732
c NNT025 Neonatal Systemic Lupus Erythematosus 14 0.036
733
c INF055 Infectious Myocarditis 15 0.036
734
TRC023 Trichinosis 44 0.036
735
ALL009 Allergic Conjunctivitis 51 0.036
736
LMY002 Leiomyoma 56 0.036
737
BRC011 Brachial Plexus Neuropathy 32 0.036
738
DNT014 Dental Pulp Disease 36 0.036
739
c CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 36 0.036
740
FTD001 Foot Drop 34 0.036
741
P HYP120 Hypoaldosteronism 34 0.036
742
P BPL003 Bipolar Disorder 58 0.036
743
P DRM010 Dermatomyositis 59 0.036
744
P GLY013 Glycogen Storage Disease 58 0.036
745
P SYP003 Syphilis 51 0.036
746
c CRD093 Cardiomyopathy, Dilated, 1a 30 0.036
747
P FBR017 Fibrosarcoma 55 0.036
748
NWC001 Newcastle Disease 51 0.036
749
P RNV001 Renovascular Hypertension 46 0.036
750
MTC028 Mitochondrial Cardiomyopathy 29 0.036
751
TRM010 Traumatic Brain Injury 52 0.036
752
THL018 Thalassemia Major 31 0.036
753
ALL003 Allergic Rhinitis 67 0.036
754
P LPR003 Leprosy 70 0.036
755
MLG056 Malignant Hyperthermia 60 0.036
756
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 40 0.036
757
CMM005 Common Cold 58 0.036
758
SNS001 Sensorineural Hearing Loss 52 0.036
759
P LTR001 Lateral Sclerosis 50 0.036
760
CMB002 Combat Disorder 22 0.036
761
WLD005 Wild Type Attr Amyloidosis 18 0.036
762
END080 Endometrial Disease 42 0.036
763
P ANT001 Anterolateral Myocardial Infarction 17 0.036
764
DGT004 Digitalis Poisoning 11 0.036
765
c LNG092 Long Qt Syndrome-3 36 0.036
766
HMF006 Hemifacial Microsomia 54 0.036
767
P SJG001 Sjogren's Syndrome 55 0.036
768
PRL009 Prolactinoma 63 0.036
769
ADM013 Adamantinoma of Long Bones 57 0.036
770
CRS005 Crest Syndrome 37 0.036
771
NLS001 Nelson Syndrome 43 0.036
772
DFF003 Diffuse Scleroderma 39 0.036
773
SBS003 Substance Abuse 54 0.036
774
SCR015 Scarlet Fever 37 0.036
775
OBS001 Obstructive Jaundice 47 0.036
776
PYL006 Pyloric Stenosis 46 0.036
777
LNS003 Lens Disease 37 0.035
778
INT253 Intestinal Benign Neoplasm 48 0.035
779
RCT017 Rectal Disease 35 0.035
780
URT037 Urethral Stricture 33 0.035
781
ATT013 Attention Deficit-Hyperactivity Disorder 69 0.035
782
SMT004 Smith-Lemli-Opitz Syndrome 66 0.035
783
LPT001 Leptospirosis 65 0.035
784
MTN003 Motion Sickness 48 0.035
785
c VNT026 Ventricular Septal Defect 2 24 0.035
786
TRN012 Transient Global Amnesia 38 0.035
787
ESP020 Esophageal Atresia 48 0.035
788
ANG020 Angiosarcoma 53 0.035
789
STR029 Sternal Cleft 19 0.035
790
IMM127 Immune System Cancer 41 0.035
791
DSS024 Disease of Anatomical Entity 40 0.035
792
CRY002 Cryptorchidism 61 0.035
793
BNC003 Bone Cancer 44 0.035
794
P INT030 Intracranial Aneurysm 52 0.035
795
MCR103 Microtia 37 0.035
796
WRT002 Writing Disorder 26 0.035
797
PHN003 Phenylketonuria 71 0.034
798
PLY125 Polycythemia Vera, Somatic 63 0.034
799
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 38 0.034
800
P KLP003 Klippel-Feil Syndrome 47 0.034
801
P CRN037 Craniosynostosis 66 0.034
802
ABR009 Abruzzo-Erickson Syndrome 34 0.034
803
FCL012 Facial Paralysis 50 0.034
804
c CRD199 Cardiomyopathy, Hypertrophic 6 29 0.034
805
GST037 Gastroparesis 54 0.034
806
DNG002 Dengue Hemorrhagic Fever 60 0.034
807
c HPT007 Hepatitis E 51 0.034
808
VGN023 Vaginitis 41 0.034
809
VGS001 Vagus Nerve Disease 17 0.034
810
CLC001 Calciphylaxis 40 0.034
811
P MTH007 Methemoglobinemia 44 0.034
812
ANR010 Aneurysm of Sinus of Valsalva 21 0.034
813
VSL002 Visual Epilepsy 30 0.034
814
ART013 Aortic Malignant Tumor 15 0.034
815
INT011 Interstitial Emphysema 37 0.034
816
CNT098 Central Core Disease 68 0.033
817
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.033
818
P PRS038 Personality Disorder 60 0.033
819
P HMP007 Hemophilia 55 0.033
820
c VNT024 Ventricular Septal Defect 3 25 0.033
821
BRN004 Brain Edema 51 0.033
822
THY001 Thyroid Crisis 29 0.033
823
P CTN003 Cutaneous Lupus Erythematosus 49 0.033
824
CRT061 Cor Triatriatum Dexter 17 0.033
825
P PYL005 Pyelonephritis 52 0.033
826
CRP017 Carpal Tunnel Syndrome, Familial 44 0.033
827
c LNG050 Long Qt Syndrome 5 43 0.033
828
DYS073 Dysphagia 51 0.033
829
c ANR038 Anorexia Nervosa 1 28 0.033
830
GLS004 Glossopharyngeal Neuralgia 33 0.033
831
P BRS044 Breast Adenocarcinoma 58 0.033
832
CRV043 Cervical Dystonia 43 0.033
833
MDN002 Median Neuropathy 29 0.033
834
OVR077 Overuse Syndrome 19 0.033
835
RPT005 Repetitive Motion Disorders 16 0.033
836
CNG059 Congenital Arteriovenous Shunt 9 0.033
837
WHP002 Whiplash 35 0.033
838
P TCL004 T-Cell Leukemia 44 0.033
839
GST092 Gastroesophageal Reflux 62 0.033
840
P HYD006 Hydrocephalus 68 0.033
841
ABL002 Ablepharon-Macrostomia Syndrome 51 0.033
842
GTR002 Goiter 54 0.033
843
OCL011 Ocular Motility Disease 41 0.033
844
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 33 0.033
845
RNL007 Renal Tubular Acidosis 50 0.033
846
c ATM011 Autoimmune Hepatitis 62 0.033
847
PTT009 Pituitary Gland Disease 45 0.033
848
CRY004 Cryoglobulinemia 47 0.033
849
P HMR012 Hemorrhagic Fever 55 0.033
850
ADN002 Adenoiditis 38 0.033
851
c SYS038 Systemic Lupus Erythematosus 2 26 0.033
852
VNT001 Ventilation Pneumonitis 35 0.033
853
SMN007 Seminoma 45 0.033
854
HNS001 Hansen's Disease 30 0.033
855
SPN119 Spondylarthropathy 46 0.033
856
ISC002 Ischemic Optic Neuropathy 45 0.033
857
SNG009 Single Ventricular Septal Defect 28 0.033
858
c CHR090 Chronic Lymphocytic Leukemia 73 0.033
859
c MYP072 Myopathy, Myofibrillar, 1 39 0.033
860
AMN002 Amino Acid Metabolic Disorder 48 0.033
861
P GST049 Gastrointestinal System Cancer 59 0.033
862
c BRG006 Brugada Syndrome 2 31 0.033
863
CVR006 Cavernous Hemangioma 46 0.033
864
CLL003 Cellulitis 49 0.033
865
DSS010 Dissociative Disorder 36 0.033
866
PRN011 Pernicious Anemia 41 0.033
867
c INF023 Inflammatory Breast Carcinoma 44 0.033
868
FNC005 Functional Colonic Disease 32 0.033
869
PTT037 Pituitary Tumors 45 0.033
870
GLL022 Guillain-Barre Syndrome 58 0.032
871
P HML002 Hemolytic Anemia 60 0.032
872
c BRG009 Brugada Syndrome 7 23 0.032
873
IMP002 Imperforate Anus 54 0.032
874
c VRL010 Viral Hepatitis 60 0.032
875
HRT033 Heart-Hand Syndrome, Spanish Type 15 0.032
876
RSP002 Respiratory Syncytial Virus Infectious Disease 31 0.032
877
BRN056 Bronchopulmonary Dysplasia 56 0.032
878
KDN013 Kidney Hypertrophy 32 0.032
879
P MDL005 Medulloblastoma 76 0.031
880
MLT021 Multiple System Atrophy 71 0.031
881
NWB001 Newborn Respiratory Distress Syndrome 47 0.031
882
RYS001 Reye Syndrome 51 0.031
883
CNT047 Contact Dermatitis 62 0.031
884
c SYS043 Systemic Lupus Erythematosus 1 29 0.031
885
RSP007 Respiratory Distress Syndrome, Infant 26 0.031
886
c ATR061 Atrial Fibrillation, Familial, 10 29 0.031
887
c ACT073 Acute Leukemia 61 0.031
888
P OVR049 Ovarian Disease 54 0.031
889
P OVR046 Ovarian Cyst 48 0.031
890
MYF002 Myofascial Pain Syndrome 38 0.031
891
P UVT001 Uveitis 60 0.031
892
c MLG036 Malignant Spiradenoma 33 0.031
893
P MNN007 Meningocele 37 0.031
894
HYP085 Hypothalamic Disease 43 0.031
895
URN010 Urinary Tract Obstruction 53 0.031
896
BCT015 Bacteremia 50 0.031
897
c JVN024 Juvenile Hereditary Hemochromatosis 30 0.031
898
ANT013 Anterior Spinal Artery Syndrome 27 0.031
899
CYS003 Cystitis Cystica 31 0.031
900
c ADL080 Adult Acute Respiratory Distress Syndrome 21 0.031
901
P RFS001 Refsum Disease 60 0.031
902
NRL016 Neural Tube Defects 76 0.031
903
P TMP003 Temporal Arteritis 61 0.031
904
P BDD001 Budd-Chiari Syndrome 52 0.031
905
YLL002 Yellow Fever 58 0.031
906
ALP008 Alopecia 56 0.031
907
ACT058 Active Peptic Ulcer Disease 44 0.031
908
P DRR001 Diarrhea 60 0.031
909
ANR004 Anuria 46 0.031
910
PRT038 Protein-Energy Malnutrition 48 0.031
911
c ATR064 Atrioventricular Septal Defect 3 20 0.031
912
YNG002 Young Syndrome 25 0.031
913
P HYP009 Hypertrophic Pyloric Stenosis 40 0.031
914
SKL014 Skeletal Dysplasia 44 0.031
915
P CHL066 Cholangitis 48 0.031
916
PRM008 Parametritis 28 0.031
917
ISC001 Ischemic Neuropathy 33 0.031
918
SKL017 Skeletal Dysplasias 41 0.031
919
ADR013 Adrenal Gland Hyperfunction 47 0.030
920
c BRN108 Branchiootic Syndrome 1 36 0.030
921
c CLR085 Colorectal Cancer 1 39 0.030
922
ASP003 Aseptic Meningitis 51 0.030
923
DBT062 Diabetic Foot Ulcers 55 0.030
924
GGN002 Gigantism 29 0.030
925
HRN022 Hearing Loss/deafness 23 0.030
926
c PNC108 Pancreatitis, Hereditary 59 0.030
927
P HMP002 Hemophagocytic Lymphohistiocytosis 64 0.030
928
P EHL001 Ehlers-Danlos Syndrome 61 0.030
929
BLR007 Biliary Tract Neoplasm 49 0.030
930
P KRT007 Keratoconus 48 0.030
931
INS001 Insulinoma 60 0.030
932
HTC002 Hutchinson-Gilford Progeria 51 0.030
933
LGD001 Leg Dermatosis 17 0.030
934
BRN018 Borna Disease 43 0.030
935
c TRN008 Transient Arthropathy 13 0.030
936
c GLL026 Gallbladder Disease 3 18 0.030
937
c ATM007 Autoimmune Disease of Central Nervous System 29 0.030
938
PRS126 Prostate Cancer Susceptibility 30 0.030
939
c GLY008 Glycogen Storage Disease Ii 59 0.029
940
P OST005 Osteogenesis Imperfecta 68 0.029
941
CMM004 Common Variable Immunodeficiency 68 0.029
942
APH001 Aphthous Stomatitis 62 0.029
943
P ADM011 Adams-Oliver Syndrome 51 0.029
944
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 55 0.029
945
P IGN003 Iga Nephropathy 1 31 0.029
946
HYP080 Hypogonadism 54 0.029
947
CHK001 Chikungunya 49 0.029
948
CHL068 Cholestasis 57 0.029
949
OCL009 Ocular Cancer 61 0.029
950
DBT084 Diabetes Mellitus, Ketosis-Prone 28 0.029
951
PST095 Post-Thrombotic Syndrome 48 0.029
952
OLV002 Oliver Syndrome 44 0.029
953
NNT024 Neonatal Stroke 34 0.029
954
SPN035 Spindle Cell Sarcoma 48 0.029
955
PLC005 Placental Insufficiency 50 0.029
956
c CHR020 Chronic Interstitial Cystitis 40 0.029
957
CNG368 Congenital Adrenal Hyperplasia 60 0.029
958
c INF071 Inflammatory Bowel Disease 1 51 0.029
959
CHR322 Choreoathetosis, Hypothyroidism, and Neonatal Respiratory Distress 43 0.029
960
c BRG007 Brugada Syndrome 5 37 0.029
961
LST001 Listeriosis 53 0.029
962
P EXP004 Exophthalmos 56 0.029
963
UTR039 Uterine Fibroid 55 0.029
964
CDS001 Cadasil 50 0.029
965
c PRS116 Prostate Cancer 1 39 0.029
966
IMM062 Immunodeficiency 11 27 0.029
967
SPN027 Spinal Stenosis 55 0.029
968
P PRM006 Primary Biliary Cirrhosis 55 0.029
969
P THY054 Thyrotoxic Periodic Paralysis 46 0.029
970
P HYP004 Hypercalcemia 54 0.029
971
HPT022 Hepatoblastoma 57 0.029
972
P BRN120 Bronchus Cancer 43 0.029
973
P CTN015 Cutaneous T Cell Lymphoma 41 0.029
974
MTR031 Motor Neuro-Ophthalmic Disorders 22 0.029
975
PSD009 Pseudohermaphroditism 39 0.029
976
INF009 Inflammatory Spondylopathy 18 0.029
977
RTN020 Retinal Vascular Disease 49 0.029
978
CCN001 Cocaine Dependence 47 0.029
979
FBR032 Fibromuscular Dysplasia 39 0.029
980
c FML156 Familial Hyperaldosteronism 35 0.029
981
c SYS046 Systemic Lupus Erythematosus 3 22 0.029
982
PLY020 Polyradiculoneuropathy 42 0.029
983
P PRK057 Parkinson Disease, Late-Onset 72 0.028
984
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 60 0.028
985
EWN003 Ewing Sarcoma 63 0.028
986
VNW007 Von Willebrand Disease 57 0.028
987
P ALP009 Alopecia Areata 62 0.028
988
ARR026 Arrhythmogenic Right Ventricular Dysplasia 1 26 0.028
989
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 54 0.028
990
P MYP006 Myopia 58 0.028
991
P BRN009 Burning Mouth Syndrome 54 0.028
992
c SCK022 Sick Sinus Syndrome 3 20 0.028
993
BLM002 Bulimia Nervosa 54 0.028
994
NPH003 Nephrocalcinosis 47 0.028
995
FBR028 Fibrosing Mediastinitis 24 0.028
996
c CNG027 Congenital Hemolytic Anemia 46 0.028
997
HYP064 Hypogonadotropism 38 0.028
998
FDL001 Fiedler's Myocarditis 23 0.028
999
MYX011 Myxozoa 18 0.028
1000
FLL008 Folliculitis 47 0.028
1001
EPD016 Epidermolysis Bullosa 59 0.027
1002
P LNG064 Lung Cancer Susceptibility 3 62 0.027
1003
RTN018 Retinal Disease 55 0.027
1004
P LSS002 Lissencephaly 48 0.027
1005
TXC002 Toxic Encephalopathy 52 0.027
1006
NSP002 Nasopharyngitis 39 0.027
1007
VGN020 Vaginal Disease 42 0.027
1008
DFF005 Diffuse Large B-Cell Lymphoma 57 0.027
1009
ACL001 Acalculous Cholecystitis 35 0.027
1010
c FML191 Familial Long Qt Syndrome 39 0.027
1011
MRP001 Morphine Dependence 42 0.027
1012
CNT067 Central Cord Syndrome 22 0.027
1013
P ALZ034 Alzheimer Disease 92 0.027
1014
P ATX030 Ataxia-Telangiectasia 78 0.027
1015
PRP084 Propionicacidemia 59 0.027
1016
ICH002 Ichthyosis Bullosa of Siemens 44 0.027
1017
KRT004 Keratitis 70 0.027
1018
P CRN038 Carney Complex Variant 53 0.027
1019
P HYP345 Hyper-Ige Recurrent Infection Syndrome 54 0.027
1020
c LNG047 Long Qt Syndrome 2 42 0.027
1021
URT039 Urticaria 58 0.027
1022
FCS012 Facioscapulohumeral Muscular Dystrophy 1 50 0.027
1023
CRN041 Carnitine-Acylcarnitine Translocase Deficiency 42 0.027
1024
STR081 Stormorken Syndrome 50 0.027
1025
RYN001 Raynaud Disease 41 0.027
1026
c LNG053 Long Qt Syndrome 9 34 0.027
1027
BLL006 Bullous Pemphigoid 59 0.027
1028
c LNG056 Long Qt Syndrome 12 28 0.027
1029
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 29 0.027
1030
HYP343 Hypothryoidism, Congenital, Nongoitrous 4 40 0.027
1031
c LNG098 Long Qt Syndrome 14 42 0.027
1032
c SCL052 Scleroderma, Familial Progressive 27 0.027
1033
PST021 Postpartum Depression 49 0.027
1034
RTR001 Retrograde Amnesia 40 0.027
1035
CHR074 Choriocarcinoma 45 0.027
1036
LRY026 Laryngeal Cleft 28 0.027
1037
LPD009 Lipid Storage Disease 49 0.027
1038
c SBC007 Subacute Thyroiditis 42 0.027
1039
MXD023 Mixed Cell Type Cancer 45 0.027
1040
SDD008 Sudden Sensorineural Hearing Loss 30 0.027
1041
TSH001 Tsh Producing Pituitary Tumor 36 0.027
1042
CHR100 Chronic Ulcer of Skin 32 0.027
1043
BRN039 Bronchial Neoplasm 35 0.027
1044
TRT001 Teratocarcinoma 35 0.027
1045
MYC013 Mycobacterium Abscessus 41 0.027
1046
RTT004 Rete Testis Adenocarcinoma 27 0.027
1047
BTN004 Biotin Deficiency 34 0.027
1048
PRK010 Porokeratosis of Mibelli 32 0.027
1049
SYN005 Synostosis 44 0.027
1050
HYP070 Hyperpituitarism 40 0.027
1051
SPS007 Spastic Cerebral Palsy 42 0.027
1052
RTT005 Rete Testis Neoplasm 23 0.027
1053
MNN021 Meningococcemia 35 0.027
1054
PTR006 Peters Anomaly 64 0.026