Search results for "heart block"

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

1499 hits were found for 'heart block'

# Family MCID Name MIFTS Score
1
c HRT021 Heart Block, Progressive, Type Ia 44 7.734
2
c PRG043 Progressive Familial Heart Block, Type Ib 28 6.990
3
P HRT035 Heart Block, Congenital 38 6.700
4
c PRG126 Progressive Familial Heart Block 43 4.597
5
c PRG101 Progressive Familial Heart Block, Type Ii 25 4.412
6
ATR060 Atrial Standstill, Digenic 51 3.805
7
c FML250 Familial Progressive Cardiac Conduction Defect 28 3.410
8
SCN049 Second-Degree Atrioventricular Block 24 3.291
9
P ATR081 Atrial Standstill 37 1.986
10
SNR013 Sino-Auricular Heart Block 4 1.983
11
P HRT032 Heart Disease 75 0.713
12
CNG034 Congestive Heart Failure 72 0.463
13
P MYC007 Myocardial Infarction 79 0.312
14
ISC006 Ischemic Heart Disease 68 0.311
15
RGH001 Right Bundle Branch Block 44 0.304
16
c CRN174 Coronary Heart Disease 2 20 0.278
17
P CRD011 Cardiomyopathy 68 0.272
18
c CRN172 Coronary Heart Disease 3 19 0.267
19
SYS003 Systolic Heart Failure 43 0.256
20
P CRN211 Coronary Artery Disease 74 0.252
21
PRP027 Peripheral Vascular Disease 69 0.251
22
c CRN175 Coronary Heart Disease 4 19 0.246
23
ATR057 Atrioventricular Block 49 0.240
24
P CRN178 Coronary Heart Disease 6 21 0.240
25
c CRN214 Coronary Heart Disease 5 22 0.224
26
ISC004 Ischemia 61 0.223
27
END072 Endotheliitis 42 0.221
28
DST006 Diastolic Heart Failure 46 0.220
29
P HYP055 Hypoplastic Left Heart Syndrome 61 0.216
30
ART111 Artery Disease 55 0.205
31
c PND001 Pain Disorder 54 0.203
32
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.199
33
P ATR011 Atrial Fibrillation 66 0.185
34
c ACT075 Acute Myocardial Infarction 60 0.183
35
ART021 Arteriosclerosis 58 0.179
36
P NRP001 Neuropathy 59 0.164
37
MSC004 Muscle Tissue Disease 34 0.164
38
HYP006 Hypertensive Heart Disease 50 0.163
39
SNG003 Single Ventricular Heart 22 0.162
40
ACR041 Acromelic Frontonasal Dysostosis 45 0.155
41
HRT012 Heart Valve Disease 40 0.155
42
c CRN173 Coronary Heart Disease 8 18 0.154
43
BRT030 Birth Defects 43 0.151
44
P MYP004 Myopathy 67 0.151
45
c DLT002 Dilated Cardiomyopathy 76 0.150
46
P RSP003 Respiratory Failure 71 0.150
47
PRP080 Peripheral Artery Disease 37 0.149
48
ATH003 Atherosclerosis 65 0.145
49
P MYC008 Myocarditis 54 0.142
50
ATN002 Autonomic Nervous System Disease 48 0.142
51
P OBS005 Obesity 92 0.141
52
P ART022 Arthritis 75 0.141
53
P PLM037 Pulmonary Hypertension 79 0.140
54
RSP006 Respiratory System Disease 58 0.138
55
RHM028 Rheumatic Heart Disease 50 0.138
56
VSC007 Vascular Disease 67 0.137
57
BCK006 Back Pain 43 0.135
58
P MSC033 Muscle Disorders 52 0.135
59
PRP019 Peripheral Nervous System Disease 55 0.134
60
STR067 Stroke, Ischemic 75 0.131
61
P BRS047 Breast Cancer 100 0.130
62
c CRN177 Coronary Heart Disease 7 20 0.129
63
P SLP006 Sleep Apnea 61 0.129
64
P CHR345 Chronic Pain 50 0.127
65
UNV002 Univentricular Heart 26 0.126
66
HRT007 Heart Cancer 46 0.125
67
P HPT021 Hepatitis 69 0.124
68
RHM001 Rheumatic Fever 54 0.123
69
SLP005 Sleep Disorder 53 0.121
70
ART017 Aortic Disease 57 0.121
71
NRN002 Neuronitis 41 0.119
72
P HRT017 Heart Tumor 32 0.119
73
ANR040 Aneurysm 57 0.118
74
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.118
75
VND001 Vein Disease 47 0.118
76
c AST037 Asthma 1 29 0.118
77
CNN005 Connective Tissue Disease 62 0.117
78
P END033 Endocarditis 54 0.117
79
c MYC058 Myocardial Infarction 2 28 0.117
80
NRM005 Neuromuscular Disease 56 0.116
81
P KDN018 Kidney Disease 66 0.116
82
P NRV006 Nervous System Cancer 60 0.116
83
HYP266 Hypoxia 56 0.115
84
c AST039 Asthma 2 28 0.115
85
SPN369 Spinal Disease 39 0.114
86
SYN036 Syncope 47 0.114
87
IMP003 Impaired Renal Function Disease 34 0.114
88
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.113
89
THR024 Thrombosis 57 0.113
90
c ADL079 Adult Heart Tumor 16 0.113
91
c CHR089 Chronic Kidney Failure 66 0.112
92
RHM027 Rheumatic Disease 58 0.112
93
PHY002 Physical Disorder 43 0.112
94
c HYP595 Hypertension, Essential 69 0.110
95
c FML001 Familial Atrial Fibrillation 58 0.110
96
LNG099 Lung Disease 64 0.110
97
SDD007 Sudden Cardiac Death 47 0.109
98
P VNT002 Ventricular Septal Defect 60 0.109
99
P THY032 Thyroiditis 54 0.108
100
P HYP086 Hypothyroidism 64 0.108
101
P LPS004 Lupus Erythematosus 64 0.107
102
NTR005 Nutritional Deficiency Disease 36 0.107
103
INF013 Inferior Myocardial Infarction 35 0.107
104
c CHR096 Chronic Pulmonary Heart Disease 40 0.105
105
P SCK002 Sick Sinus Syndrome 50 0.105
106
ANG054 Angina Pectoris 50 0.105
107
P ART023 Arthropathy 64 0.104
108
PRP021 Peripheral Nervous System Neoplasm 46 0.104
109
c CRN176 Coronary Heart Disease 9 18 0.104
110
ATN005 Autonomic Dysfunction 49 0.103
111
CRN030 Coronary Stenosis 51 0.102
112
LRN003 Learning Disability 49 0.102
113
CRB039 Cerebrovascular Disease 63 0.101
114
ANX002 Anxiety Disorder 67 0.101
115
BNF002 Bone Fracture 50 0.101
116
HV1006 Hiv-1 80 0.101
117
PCK002 Pick Disease 68 0.101
118
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 57 0.100
119
BLD053 Blood Platelet Disease 46 0.100
120
P LKM002 Leukemia 71 0.100
121
c CNT015 Central Sleep Apnea 44 0.100
122
P SPS003 Spastic Diplegia 52 0.100
123
P CLL015 Collagen Disease 50 0.099
124
P LYM118 Lymphoma 69 0.099
125
CRT057 Critical Congenital Heart Disease 20 0.099
126
P ACT080 Acute Pulmonary Heart Disease 31 0.098
127
CRB031 Cerebral Arterial Disease 27 0.098
128
PRS047 Prostatitis 56 0.098
129
P URF003 Urofacial Syndrome 1 50 0.098
130
URN009 Urinary System Disease 50 0.097
131
CRD119 Cardiac Arrest 61 0.097
132
SNS023 Sensory System Cancer 43 0.097
133
P RHM011 Rheumatoid Arthritis 89 0.097
134
GNR004 Generalized Anxiety Disorder 51 0.097
135
P LNG028 Long Qt Syndrome 64 0.096
136
P AST005 Asthma 82 0.096
137
END030 End Stage Renal Failure 55 0.096
138
HDC001 Headache 54 0.096
139
c ACT071 Acute Kidney Failure 49 0.095
140
GLC008 Glucose Metabolism Disease 42 0.095
141
CRD118 Cardiovascular Cancer 44 0.095
142
JNT002 Joint Disorders 55 0.094
143
P NRV007 Nervous System Disease 71 0.093
144
ALN001 Aland Island Eye Disease 45 0.093
145
P OST012 Osteoarthritis 83 0.093
146
MNT002 Mental Depression 53 0.093
147
P PNC044 Pancreatitis 61 0.093
148
AYM001 Ayme-Gripp Syndrome 41 0.092
149
PRD011 Proud Syndrome 42 0.092
150
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 54 0.092
151
ALR002 Al-Raqad Syndrome 36 0.092
152
THR099 Third-Degree Atrioventricular Block 32 0.091
153
CRB009 Cerebritis 39 0.091
154
c SYS001 Systemic Lupus Erythematosus 86 0.091
155
ADJ001 Adjustment Disorder 38 0.091
156
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.090
157
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.090
158
MVM001 Movement Disease 49 0.090
159
P MSC005 Muscular Dystrophy 65 0.090
160
CRD003 Cardiac Sarcoidosis 42 0.089
161
DXT001 Dextrocardia 43 0.089
162
P CRD132 Cardiac Conduction Defect 43 0.088
163
VSC047 Vascular Malformation 45 0.088
164
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.088
165
TTR001 Tetralogy of Fallot 71 0.088
166
FRS012 First-Degree Atrioventricular Block 30 0.087
167
VNT011 Ventricular Fibrillation, Familial, 1 41 0.087
168
c TRC078 Trichohepatoenteric Syndrome 2 29 0.087
169
P INF032 Infertility 59 0.087
170
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.086
171
CRB004 Cerebral Artery Occlusion 45 0.086
172
P LNG032 Lung Cancer 95 0.086
173
OBS061 Obstructive Sleep Apnea 66 0.086
174
P MTR012 Mitral Valve Disease 58 0.086
175
RNL097 Renal Artery Disease 43 0.086
176
c ACT076 Acute Myocarditis 42 0.085
177
P PRS040 Prostate Cancer 90 0.084
178
INF034 Infective Endocarditis 51 0.084
179
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.084
180
CSY001 C Syndrome 50 0.083
181
MLN008 Melanoma 62 0.083
182
MSC072 Muscle Cancer 49 0.083
183
CHL071 Child Syndrome 58 0.082
184
KDS001 Kid Syndrome 53 0.082
185
LPD008 Lipid Metabolism Disorder 58 0.082
186
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.082
187
MTH009 Mouth Disease 61 0.082
188
CND002 Conduct Disorder 54 0.081
189
END040 Endogenous Depression 53 0.081
190
ALL026 Allergic Hypersensitivity Disease 52 0.081
191
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.081
192
TRN044 Transposition of the Great Arteries 48 0.081
193
P PNM007 Pneumonia 68 0.080
194
SRC014 Sarcoma 66 0.080
195
ATN004 Autonomic Neuropathy 45 0.080
196
NSL022 Nasal Cavity Disease 38 0.080
197
DPH021 Diaphragm Disease 41 0.080
198
LPD004 Lipoid Nephrosis 48 0.080
199
PRN021 Paranasal Sinus Disease 49 0.079
200
P BRG001 Brugada Syndrome 59 0.079
201
INT007 Intermediate Coronary Syndrome 50 0.079
202
BRN080 Brain Ischemia 41 0.079
203
c ART101 Aortic Valve Disease 2 53 0.079
204
PLM129 Pulmonary Disease, Chronic Obstructive 63 0.078
205
WLF001 Wolff-Parkinson-White Syndrome 56 0.078
206
WTH001 Withdrawal Disorder 37 0.078
207
GDS001 Good Syndrome 44 0.077
208
P LVR013 Liver Disease 75 0.077
209
PLM033 Pulmonary Embolism 60 0.077
210
TTH006 Tooth Disease 52 0.077
211
P INF038 Influenza 72 0.076
212
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.076
213
BLD054 Blood Protein Disease 37 0.075
214
WLL006 Wells Syndrome 59 0.075
215
ADL002 Adult Syndrome 52 0.075
216
DSS008 Disease of Mental Health 52 0.075
217
P CRV039 Cervicitis 45 0.074
218
PLM010 Pulmonary Edema 54 0.074
219
KRN002 Kearns-Sayre Syndrome 61 0.074
220
P DYS021 Dysautonomia 44 0.074
221
HRT008 Heart Conduction Disease 42 0.074
222
P HPT023 Hepatocellular Carcinoma 92 0.074
223
ING001 Inguinal Hernia 58 0.074
224
P AMY004 Amyloidosis 65 0.074
225
c CNT068 Central Pain Syndrome 29 0.073
226
CRN073 Coronary Arteries Congenital Malformation 10 0.073
227
P RST002 Restrictive Cardiomyopathy 50 0.072
228
END020 Endocardial Fibroelastosis 44 0.072
229
CRN017 Coronary Thrombosis 48 0.072
230
P PLM040 Pulmonary Valve Disease 43 0.072
231
P MSC007 Muscle Hypertrophy 58 0.072
232
SPC003 Specific Developmental Disorder 38 0.071
233
P ENC018 Encephalopathy 59 0.071
234
P RNL015 Renal Hypertension 48 0.071
235
c CNG031 Congenital Nervous System Abnormality 37 0.071
236
P ADN016 Adenocarcinoma 69 0.071
237
CRT016 Carotid Artery Disease 57 0.071
238
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.070
239
HYP540 Hypertension, Diastolic 39 0.070
240
P MLT019 Multiple Myeloma 83 0.070
241
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.070
242
MDY003 Mody, Type Ii 36 0.070
243
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 21 0.070
244
MRG013 Mirage Syndrome 29 0.069
245
MLR004 Malaria 83 0.069
246
SXL003 Sexual Disorder 42 0.069
247
INS024 Insulin-Like Growth Factor I 75 0.069
248
BRN071 Brain Injury 52 0.069
249
CRD137 Cardiogenic Shock 46 0.069
250
DFC004 Deficiency Anemia 64 0.068
251
c MTR002 Mitral Valve Insufficiency 44 0.068
252
c HPT001 Hepatitis C 68 0.068
253
CHG001 Chagas Disease 67 0.068
254
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 53 0.068
255
SKN016 Skin Disease 66 0.068
256
EXF001 Exfoliation Syndrome 57 0.068
257
c VNT013 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1 49 0.068
258
NSD001 Nose Disease 48 0.068
259
BNS002 Bone Structure Disease 37 0.067
260
TBR010 Tuberculosis 70 0.066
261
SKN023 Skin Tag 44 0.066
262
P PLN008 Peeling Skin Syndrome 45 0.066
263
VSC006 Vascular Cancer 51 0.066
264
ATR024 Atrial Fibrillation and Stroke 22 0.066
265
VSC009 Vascular Skin Disease 19 0.066
266
VSC008 Vascular Hemostatic Disease 30 0.066
267
CMP010 Complex Regional Pain Syndrome 54 0.066
268
P NNT042 Neonatal Lupus Erythematosus 34 0.066
269
CTS003 Coats Disease 57 0.065
270
PRC013 Pericarditis 51 0.065
271
MLR007 Male Reproductive System Disease 34 0.065
272
ART016 Aortic Aneurysm 69 0.065
273
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.064
274
MDS022 Mediastinitis 41 0.064
275
P MYT002 Myotonic Dystrophy 48 0.064
276
BRN028 Brain Cancer 70 0.064
277
P EPL164 Epilepsy 66 0.063
278
HYP066 Hyperglycemia 61 0.063
279
ANX004 Anoxia 43 0.063
280
MYX004 Myxedema 35 0.063
281
P CLR023 Colorectal Cancer 97 0.063
282
PNM008 Pneumothorax 53 0.063
283
RDN001 Reading Disorder 34 0.063
284
c HPT073 Hepatitis C Virus 73 0.063
285
THY030 Thyroid Gland Disease 48 0.062
286
c ART115 Aortic Valve Disease 1 50 0.062
287
c ATM022 Autoimmune Myocarditis 42 0.062
288
HTR003 Heterotaxy 44 0.062
289
BRS051 Breast Disease 61 0.062
290
P LFT003 Left Ventricular Noncompaction 50 0.061
291
PRC012 Pericardial Effusion 51 0.061
292
P PLY019 Polyneuropathy 56 0.061
293
HYP005 Hypokalemia 51 0.061
294
UPP004 Upper Respiratory Tract Disease 46 0.061
295
ACD009 Acid-Labile Subunit, Deficiency of 45 0.061
296
CRT015 Carotid Artery Occlusion 43 0.061
297
ETN001 Eating Disorder 58 0.061
298
MDD011 Mood Disorder 61 0.060
299
WST001 West Syndrome 57 0.060
300
PRP009 Peripartum Cardiomyopathy 42 0.060
301
OVR063 Overnutrition 50 0.060
302
PNC034 Pancreas Disease 58 0.060
303
P HLT001 Holt-Oram Syndrome 61 0.060
304
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.060
305
SKN027 Skin Conditions 43 0.060
306
P HRP006 Herpes Simplex 65 0.060
307
MYC002 Mycobacterium Avium Complex Disease 52 0.060
308
MYC005 Myocardial Stunning 44 0.060
309
CRD001 Cardiac Tamponade 44 0.060
310
PLC008 Placenta Disease 33 0.059
311
P CTR002 Cataract 58 0.059
312
DBT002 Diabetic Autonomic Neuropathy 42 0.059
313
ISC005 Ischemic Bone Disease 36 0.059
314
GNT019 Giant Cell Myocarditis 31 0.059
315
P BLD051 Blood Coagulation Disease 42 0.059
316
P MCR129 Microvascular Complications of Diabetes 1 54 0.059
317
FBR012 Fabry Disease 69 0.059
318
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 41 0.058
319
P FML035 Familial Hyperlipidemia 48 0.058
320
c PLM128 Pulmonary Hypertension, Primary, 2 28 0.058
321
SNT004 Sinoatrial Node Dysfunction and Deafness 25 0.058
322
PST028 Post-Traumatic Stress Disorder 57 0.058
323
c DYS033 Dysautonomia Like Disorder 16 0.058
324
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 56 0.058
325
STS002 Situs Inversus 46 0.058
326
FML039 Female Reproductive System Disease 48 0.058
327
PRT036 Peritonitis 63 0.058
328
P HYP076 Hyperthyroidism 55 0.058
329
PRP050 Peripheral Arterial Occlusive Disease 1 14 0.058
330
P SKN013 Skin Benign Neoplasm 43 0.058
331
TRC062 Tricuspid Atresia 43 0.058
332
P OVR042 Ovarian Cancer 76 0.058
333
BRC012 Brucellosis 66 0.058
334
P SHR029 Short Syndrome 58 0.058
335
c PLM022 Pulmonary Valve Insufficiency 34 0.058
336
c CNT035 Central Nervous System Disease 60 0.057
337
CCN007 Cocoon Syndrome 45 0.057
338
c RNL016 Renal Infectious Disease 20 0.057
339
GST053 Gastric Cancer 78 0.057
340
CPL005 Capillary Disease 36 0.057
341
c PNC106 Pancreatic Agenesis 1 37 0.056
342
ACT084 Acute Stress Disorder 40 0.056
343
P PRD008 Periodontitis 63 0.056
344
CRB087 Cerebral Arteriosclerosis 21 0.056
345
PRM025 Primary Bacterial Infectious Disease 41 0.056
346
HDN002 Head Injury 45 0.056
347
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.056
348
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.056
349
c THR092 Thrombophilia Due to Thrombin Defect 54 0.056
350
NSY001 N Syndrome 36 0.056
351
DWN001 Down Syndrome 66 0.056
352
P THR014 Thrombocytopenia 64 0.055
353
CRB085 Cerebral Hemorrhage 46 0.055
354
STM006 Stomach Disease 50 0.055
355
ART005 Arteriovenous Malformation 66 0.055
356
P CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 48 0.055
357
CNG134 Congenitally Corrected Transposition of the Great Arteries 24 0.055
358
P NRB001 Neuroblastoma 70 0.055
359
P INT070 Intestinal Obstruction 57 0.055
360
HRT006 Heart Aneurysm 24 0.055
361
PST053 Postherpetic Neuralgia 40 0.054
362
ATN003 Autonomic Nervous System Neoplasm 40 0.054
363
c PLN018 Peeling Skin Syndrome 2 40 0.054
364
EBS001 Ebstein Anomaly 45 0.054
365
P MSC003 Muscular Atrophy 50 0.054
366
PHR003 Pharyngitis 56 0.054
367
AND005 Androgen Insensitivity Syndrome, Mild 16 0.054
368
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 27 0.054
369
CRC006 Carcinoid Syndrome 52 0.054
370
RPR002 Reproductive System Disease 41 0.054
371
GLT021 Glutaricaciduria, Type I 46 0.054
372
HRT029 Heart Tumor of the Child 15 0.054
373
SNS003 Sensory Peripheral Neuropathy 45 0.054
374
BRS090 Breast Reconstruction 38 0.054
375
PLY023 Polycystic Liver Disease 56 0.054
376
c HPT016 Hepatitis B 65 0.054
377
LFT009 Left Ventricular Outflow Tract Obstruction 43 0.054
378
FML037 Female Breast Cancer 50 0.053
379
RTN023 Retinitis 50 0.053
380
ATM052 Autoimmune Disease 1 25 0.053
381
P PHC003 Pheochromocytoma 71 0.053
382
c OST147 Osteoarthritis 1 30 0.053
383
CRT028 Cor Triatriatum 22 0.053
384
SPN041 Spinal Cord Disease 51 0.053
385
P TRC086 Trichohepatoenteric Syndrome 1 48 0.053
386
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.053
387
P INT143 Interstitial Cystitis 57 0.053
388
FCL011 Facial Nerve Disease 36 0.053
389
GNC005 Geniculate Ganglionitis 27 0.053
390
CNV002 Conversion Disorder 41 0.052
391
BLD044 Bladder Disease 51 0.052
392
SPN051 Spondylitis 51 0.052
393
ADR038 Adermatoglyphia 46 0.052
394
c ACT210 Acute Respiratory Distress Syndrome 57 0.051
395
GNG013 Gingivitis 61 0.051
396
IMM136 Immune System Disease 51 0.051
397
HRT011 Heart Septal Defect 40 0.051
398
WLS001 Wilson Disease 72 0.051
399
PLM041 Pulmonary Valve Stenosis 47 0.051
400
CHN016 Cohen Syndrome 54 0.051
401
PSY004 Psychotic Disorder 67 0.051
402
VSC011 Vasculitis 62 0.051
403
P PRX010 Paroxysmal Ventricular Fibrillation 37 0.051
404
PRS036 Parasitic Protozoa Infectious Disease 41 0.051
405
C3D001 C3 Deficiency 53 0.050
406
ADR005 Adrenal Carcinoma 57 0.050
407
CYT008 Cytomegalovirus Infection 52 0.050
408
c PST001 Posterior Myocardial Infarction 31 0.050
409
P DBT005 Diabetes Insipidus 53 0.050
410
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 35 0.050
411
HYP056 Hypoglycemia 61 0.050
412
GLB001 Gilbert Syndrome 60 0.050
413
HYD012 Hydrops Fetalis 43 0.049
414
NRR001 Neuroretinitis 42 0.049
415
P TRC087 Tricuspid Valve Disease 44 0.049
416
CLT003 Colitis 60 0.049
417
LYM017 Lyme Disease 63 0.049
418
P INT068 Intestinal Disease 60 0.049
419
BRN106 Burns 52 0.049
420
P HNT016 Huntington Disease 80 0.049
421
P SYS005 Systemic Scleroderma 61 0.049
422
TYP027 Type 1 Diabetes Mellitus 10 27 0.049
423
ATM053 Autoimmune Disease 2 16 0.049
424
P HYP265 Hypotonia 38 0.049
425
HMS001 Hemosiderosis 46 0.049
426
ACT017 Acute Chest Syndrome 48 0.049
427
CRB025 Carbohydrate Metabolic Disorder 46 0.049
428
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.049
429
DMN002 Dementia 65 0.049
430
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.049
431
ALC010 Alcoholic Cardiomyopathy 38 0.049
432
P MMB011 Membranous Nephropathy 54 0.048
433
P VNS003 Venous Insufficiency 54 0.048
434
c PLN021 Peeling Skin Syndrome 3 29 0.048
435
PRS042 Prostate Disease 52 0.048
436
PRD007 Periodontal Disease 60 0.048
437
P EMR001 Emery-Dreifuss Muscular Dystrophy 55 0.048
438
CRB008 Cerebral Atherosclerosis 43 0.048
439
MNN017 Mononeuropathy 40 0.048
440
MTR007 Motor Peripheral Neuropathy 37 0.048
441
BCK001 Becker Muscular Dystrophy 69 0.048
442
IRN002 Iron Metabolism Disease 41 0.048
443
CNS004 Constipation 57 0.047
444
P KDN017 Kidney Cancer 65 0.047
445
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 33 0.047
446
CRB037 Cerebral Palsy 66 0.047
447
ATP002 Atopy 66 0.047
448
P SZR006 Seizure Disorder 56 0.047
449
ART012 Aortitis 30 0.047
450
PTN001 Patent Foramen Ovale 55 0.047
451
c SBC003 Subacute Bacterial Endocarditis 36 0.047
452
P PLM036 Pulmonary Fibrosis 71 0.047
453
ANG049 Angioedema Induced by Ace Inhibitors 34 0.047
454
PLR022 Pleural Disease 51 0.047
455
PRN037 Prinzmetal's Variant Angina 39 0.047
456
ATR055 Atrial Septal Aneurysm 24 0.047
457
P CLC005 Celiac Disease 68 0.047
458
P MYS003 Myasthenia Gravis 67 0.047
459
P GLL020 Gallbladder Disease 59 0.047
460
DBT010 Diabetic Neuropathy 55 0.047
461
SBC016 Subacute Delirium 24 0.047
462
SPS057 Spasticity 42 0.047
463
P HMN010 Hemangioma 59 0.046
464
GST050 Gastrointestinal System Disease 56 0.046
465
P ART084 Arteriovenous Fistula 44 0.046
466
P UTR038 Uterine Disease 37 0.046
467
ACT174 Acute Peripheral Arterial Occlusion 15 0.046
468
P INF037 Inflammatory Bowel Disease 63 0.046
469
SPN186 Spinal Cord Injury 63 0.046
470
P EXN002 Exanthem 57 0.046
471
c PLN017 Peeling Skin Syndrome 1 34 0.046
472
P CRN074 Coronary Artery Aneurysm 46 0.046
473
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 36 0.046
474
LMB062 Limb Ischemia 48 0.046
475
SML033 Small Cell Cancer of the Lung, Somatic 54 0.046
476
ACT094 Acute Articular Rheumatism 17 0.046
477
P ALX003 Alexander Disease 63 0.046
478
P ATR001 Atrioventricular Septal Defect 52 0.045
479
CYS001 Cystic Fibrosis 83 0.045
480
MGR028 Migraine with or Without Aura 1 47 0.045
481
MXD005 Mixed Connective Tissue Disease 62 0.045
482
THY028 Thyroid Cancer 69 0.045
483
ATM054 Autoimmune Disease 3 15 0.045
484
GNR003 Generalized Atherosclerosis 37 0.045
485
ALL006 Allergic Asthma 58 0.045
486
P LRY019 Laryngitis 54 0.045
487
ADT003 Auditory System Disease 40 0.045
488
P HYP040 Hypospadias 57 0.045
489
INC022 Inclusion-Cell Disease 46 0.045
490
P GRV001 Graves' Disease 59 0.045
491
P GLM007 Glomerulonephritis 59 0.045
492
MRF001 Marfan Syndrome 73 0.044
493
ART031 Aortic Coarctation 43 0.044
494
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 21 0.044
495
P ATX004 Ataxia 53 0.044
496
RNL001 Renal Artery Obstruction 31 0.044
497
c LNG044 Long Qt Syndrome 1 62 0.044
498
CRC034 Carcinoma Showing Thymus-Like Differentiation 21 0.044
499
CRD016 Cardiac Rupture 34 0.044
500
FNT004 Fainting 33 0.044
501
FRZ001 Frozen Shoulder 45 0.044
502
SQM006 Squamous Cell Carcinoma 70 0.044
503
HRP004 Herpes Zoster 56 0.043
504
P FNC043 Fanconi Anemia, Complementation Group E 55 0.043
505
OLV001 Olivopontocerebellar Atrophy 53 0.043
506
END038 Endocrine Pancreas Disease 41 0.043
507
CHL067 Cholecystitis 57 0.043
508
SCK005 Sickle Cell Disease 51 0.043
509
HPT074 Hepatic Adenoma, Somatic 50 0.043
510
P PLM085 Pulmonary Hemosiderosis 44 0.043
511
P PLY006 Polydactyly 56 0.043
512
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.043
513
WLL001 Williams-Beuren Syndrome 60 0.043
514
LKC003 Leukocyte Disease 43 0.043
515
c HPT003 Hepatitis a 59 0.043
516
c SVR001 Severe Acute Respiratory Syndrome 57 0.043
517
c NRP037 Neuropathy, Hereditary Sensory and Autonomic, Type V 54 0.042
518
ATN001 Autonomic Peripheral Neuropathy 17 0.042
519
RFL001 Reflex Sympathetic Dystrophy 48 0.042
520
CHL123 Chlamydia 60 0.042
521
MTB004 Metabolic Acidosis 48 0.042
522
FCT008 Factitious Disorder 41 0.042
523
c ART106 Arterial Calcification, Generalized, of Infancy, 1 39 0.042
524
CRN006 Coronary Aneurysm 32 0.042
525
MND006 Mondor Disease 21 0.042
526
CLV009 Clove Syndrome, Somatic 41 0.042
527
P ESP024 Esophagitis 61 0.042
528
BLR006 Biliary Tract Disease 52 0.042
529
END035 Endocrine Gland Cancer 49 0.042
530
TRC026 Tracheal Disease 35 0.042
531
P NPH009 Nephrolithiasis 60 0.042
532
RHB003 Rhabdomyosarcoma 57 0.042
533
PLS006 Plasmodium Vivax Malaria 53 0.042
534
DCH001 Duchenne Muscular Dystrophy 79 0.041
535
P LPS002 Liposarcoma 55 0.041
536
RNL077 Renal Fibrosis 47 0.041
537
ATM013 Autoimmune Disease of Cardiovascular System 13 0.041
538
GLC003 Glucose Intolerance 55 0.041
539
P PTN002 Patent Ductus Arteriosus 52 0.041
540
SPR035 Superior Vena Cava Syndrome 31 0.041
541
P MNN013 Meningitis 67 0.041
542
MRB003 Morbid Obesity 59 0.041
543
SNS001 Sensorineural Hearing Loss 57 0.041
544
LVR012 Liver Cirrhosis 67 0.041
545
P MYL006 Myeloid Leukemia 66 0.041
546
HND003 Hand-Foot-Uterus Syndrome 50 0.041
547
P ENC004 Encephalitis 63 0.041
548
P GST049 Gastrointestinal System Cancer 60 0.041
549
CLS010 Cluster Headache 44 0.041
550
P SCH015 Schizophrenia 77 0.041
551
P ANR007 Anorexia Nervosa 61 0.041
552
P THL005 Thalassemia 64 0.041
553
P RCK004 Rickets 61 0.041
554
c TRC022 Tricuspid Valve Insufficiency 33 0.041
555
HMP001 Hemopericardium 28 0.041
556
P ADL010 Adult Respiratory Distress Syndrome 61 0.041
557
TTN003 Tetanus 61 0.041
558
c CNG006 Congenital Hypothyroidism 60 0.041
559
BRN002 Bronchiolitis 56 0.040
560
NWC001 Newcastle Disease 54 0.040
561
TRM010 Traumatic Brain Injury 52 0.040
562
OCL006 Ocular Hypertension 48 0.040
563
RGH009 Right Atrial Isomerism 44 0.040
564
BND014 Bone Development Disease 40 0.040
565
ACR002 Acrocapitofemoral Dysplasia 33 0.040
566
P ASP006 Aspergillosis 61 0.040
567
DXT002 Dextrocardia with Situs Inversus 37 0.040
568
P RNL014 Renal Cell Carcinoma 82 0.040
569
P BCL006 B-Cell Lymphomas 65 0.040
570
URT001 Urethritis 41 0.040
571
WRN001 Werner Syndrome 67 0.040
572
SNT005 Sinoatrial Node Disease 36 0.040
573
P SPN052 Spondyloarthropathy 60 0.040
574
OCL009 Ocular Cancer 59 0.040
575
P MYS005 Myositis 57 0.040
576
GST023 Gastric Ulcer 56 0.040
577
BRN038 Bronchial Disease 51 0.040
578
DRG003 Drug Dependence 50 0.040
579
PHC013 Phaeochromocytoma 41 0.040
580
BRN055 Bronchogenic Cyst 28 0.040
581
PLS007 Plasmodium Falciparum Malaria 55 0.039
582
c SHR030 Short Qt Syndrome 44 0.039
583
SXD001 Sex Differentiation Disease 38 0.039
584
DRG001 Drug Psychosis 38 0.039
585
P FBR017 Fibrosarcoma 56 0.039
586
P LMY004 Leiomyosarcoma 55 0.039
587
PST055 Postural Hypotension 36 0.039
588
PLM001 Pulmonary Tuberculosis 67 0.039
589
CRB086 Cerebral Aneurysms 39 0.039
590
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 36 0.039
591
MYT011 Myotonia 36 0.039
592
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.039
593
HTR014 Heterotaxy, Visceral, 1, X-Linked 36 0.039
594
PST048 Postural Orthostatic Tachycardia Syndrome 27 0.038
595
c ATR075 Atrial Fibrillation 15 24 0.038
596
DRM006 Dermatitis 66 0.038
597
P SPN046 Spinal Muscular Atrophy 65 0.038
598
c MYT021 Myotonic Dystrophy 1 63 0.038
599
DPH001 Diphtheria 59 0.038
600
ADM013 Adamantinoma of Long Bones 57 0.038
601
P ARC016 Auriculocondylar Syndrome 1 40 0.038
602
P GNR027 Generalized Peeling Skin Syndrome 19 0.038
603
c CRD099 Cardiomyopathy, Dilated, 1e 52 0.038
604
P ABD003 Abdominal Aortic Aneurysm 45 0.038
605
SCK003 Sickle Cell Anemia 71 0.038
606
RBR001 Roberts Syndrome 60 0.038
607
HYP711 Hypotonia, Ataxia, and Delayed Development Syndrome 26 0.038
608
CLN019 Colonic Disease 51 0.038
609
SPT001 Septal Myocardial Infarction 15 0.038
610
P ADD001 Addison's Disease 62 0.038
611
P SML001 Small Cell Carcinoma 56 0.038
612
ESP023 Esophageal Disease 54 0.038
613
QDR001 Quadriplegia 52 0.038
614
P PTS002 Ptosis 51 0.038
615
STM007 Stomatitis 50 0.038
616
OPT006 Optic Nerve Disease 52 0.038
617
URT004 Urethral Syndrome 45 0.038
618
DCB001 Decubitus Ulcer 41 0.038
619
P OCY001 Oocyte Maturation Defect 38 0.038
620
EPD019 Epidural Neoplasm 33 0.038
621
FST001 Foster-Kennedy Syndrome 31 0.038
622
PSR001 Psoriatic Arthritis 64 0.038
623
BNC003 Bone Cancer 58 0.038
624
DYS073 Dysphagia 48 0.038
625
PRG004 Progeria 44 0.038
626
CNT017 Central Nervous System Origin Vertigo 24 0.038
627
P CHR071 Charcot-Marie-Tooth Disease 67 0.038
628
P DYS154 Dystonia 65 0.038
629
P RHN004 Rhinitis 60 0.038
630
ACH001 Acheiropody 46 0.038
631
RCT017 Rectal Disease 40 0.038
632
CNT098 Central Core Disease 65 0.037
633
BRN024 Bronchitis 64 0.037
634
INT066 Interstitial Lung Disease 59 0.037
635
c CRD093 Cardiomyopathy, Dilated, 1a 55 0.037
636
CLC006 Calcinosis 50 0.037
637
PLM068 Pulmonary Vein Stenosis 40 0.037
638
MSS002 Mass Syndrome 48 0.037
639
END074 Endocardium Disease 26 0.037
640
c SRC025 Sarcoidosis 1 61 0.037
641
TXC005 Toxic Shock Syndrome 60 0.037
642
TRN015 Transient Cerebral Ischemia 56 0.037
643
P PLY041 Polymyositis 52 0.037
644
c CHR431 Chronic Venous Insufficiency 44 0.037
645
HDG012 Hodgkin Lymphoma 77 0.037
646
PRT037 Pertussis 64 0.037
647
GNG011 Gingival Disease 46 0.037
648
P DMY001 Demyelinating Polyneuropathy 43 0.036
649
c OST112 Osteoarthritis-5 38 0.036
650
CML001 Cumulative Trauma Disorders 18 0.036
651
P TRN020 Turner Syndrome 65 0.036
652
P OST002 Osteoporosis 64 0.036
653
FTT001 Fatty Liver Disease 59 0.036
654
c ACT134 Acute Liver Failure 50 0.036
655
HPR003 Heparin-Induced Thrombocytopenia 45 0.036
656
P ATR010 Atrial Heart Septal Defect 45 0.036
657
PLS010 Plasma Protein Metabolism Disease 34 0.036
658
P DRR001 Diarrhea 60 0.036
659
P ANT006 Antiphospholipid Syndrome 56 0.036
660
P JRV003 Jervell and Lange-Nielsen Syndrome 53 0.036
661
c MCR113 Microvascular Complications of Diabetes 3 45 0.036
662
ATM012 Autoimmune Disease of Blood 35 0.036
663
HSB001 His Bundle Tachycardia 22 0.036
664
P CNJ013 Conjunctivitis 64 0.036
665
GLB003 Globe Disease 32 0.036
666
P MDL005 Medulloblastoma 77 0.036
667
ALC007 Alcohol Dependence 63 0.036
668
GST045 Gastroenteritis 59 0.036
669
MLR006 Male Reproductive Organ Cancer 43 0.036
670
P CHR102 Charcot-Marie-Tooth Neuropathy 41 0.036
671
ATM059 Autoimmune Disease 6 22 0.036
672
P MYM002 Moyamoya Disease 61 0.036
673
ALG001 Algoneurodystrophy 31 0.036
674
PRP030 Purpura 58 0.036
675
BRN012 Bronchiolitis Obliterans 58 0.036
676
P HMR012 Hemorrhagic Fever 56 0.036
677
P LMB006 Limb-Girdle Muscular Dystrophy 51 0.036
678
CHL004 Cholelithiasis 48 0.036
679
CRT013 Carotid Stenosis 36 0.036
680
ATM014 Autoimmune Disease of Endocrine System 36 0.036
681
HNM002 Hinman Syndrome 25 0.036
682
VGS001 Vagus Nerve Disease 18 0.036
683
P INT030 Intracranial Aneurysm 54 0.035
684
TMP001 Temporal Lobe Epilepsy 50 0.035
685
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 43 0.035
686
ACT058 Active Peptic Ulcer Disease 43 0.035
687
ART013 Aortic Malignant Tumor 14 0.035
688
P PLY011 Polycystic Ovary Syndrome 65 0.035
689
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 60 0.035
690
P TMT001 Timothy Syndrome 55 0.035
691
HST009 Histiocytoma 47 0.035
692
FBR003 Fibrous Histiocytoma 43 0.035
693
c PRG106 Progressive Muscular Dystrophy 40 0.035
694
TRC021 Tricuspid Valve Stenosis 39 0.035
695
P TRC005 Tracheal Stenosis 39 0.035
696
c HMG004 Hemoglobin D Disease 31 0.035
697
P HMR003 Hemorrhagic Disease 57 0.035
698
CLF001 Cleft Lip 50 0.035
699
ANR010 Aneurysm of Sinus of Valsalva 26 0.035
700
LVC002 Levocardia 18 0.035
701
ETH011 Ethylmalonic Encephalopathy 56 0.035
702
BLT006 Bilateral Breast Cancer 53 0.035
703
OCC004 Occlusion of Gallbladder 13 0.035
704
CHR103 Charge Syndrome 62 0.034
705
PRM097 Primary Immunodeficiency Disease 60 0.034
706
P CRC039 Coarctation of Aorta 34 0.034
707
RHM029 Rheumatic Fever-Related Antigen Rheumatic Fever, Acute, Susceptibility to, Included 23 0.034
708
SBS003 Substance Abuse 54 0.034
709
PRP016 Paraplegia 49 0.034
710
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 48 0.034
711
c HYP073 Hypersensitivity Reaction Type Iv Disease 43 0.034
712
GND003 Gonadal Disease 39 0.034
713
ADR009 Adrenal Cortex Disease 39 0.034
714
c SCK017 Sick Sinus Syndrome 1 29 0.034
715
YNG002 Young Syndrome 26 0.034
716
URN010 Urinary Tract Obstruction 55 0.034
717
c INF023 Inflammatory Breast Carcinoma 52 0.034
718
P ERY008 Erythromelalgia 51 0.034
719
ANK001 Ankylosis 51 0.034
720
P CMP008 Compartment Syndrome 48 0.034
721
GST078 Gastrointestinal Allergy 40 0.034
722
PRP028 Peripheral Vertigo 38 0.034
723
PRM243 Primary Bone Cancer 29 0.034
724
ATM055 Autoimmune Disease 4 15 0.034
725
MSL001 Measles 61 0.034
726
VGN020 Vaginal Disease 41 0.034
727
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 33 0.034
728
ANT005 Anteroseptal Myocardial Infarction 22 0.034
729
P RFS001 Refsum Disease 63 0.034
730
APH001 Aphthous Stomatitis 62 0.034
731
P ALC004 Alcohol Abuse 59 0.034
732
NRN004 Neuroendocrine Tumor 56 0.034
733
PLM034 Pulmonary Emphysema 55 0.034
734
P HYP065 Hyperaldosteronism 50 0.034
735
DBT084 Diabetes Mellitus, Ketosis-Prone 47 0.034
736
KDN013 Kidney Hypertrophy 31 0.034
737
HRT033 Heart-Hand Syndrome, Spanish Type 15 0.034
738
MLG056 Malignant Hyperthermia 58 0.034
739
c ATS347 Autosomal Dominant Polycystic Kidney Disease 63 0.033
740
P SDD001 Sudden Infant Death Syndrome 61 0.033
741
VRL011 Viral Infectious Disease 55 0.033
742
ANG020 Angiosarcoma 53 0.033
743
P TRT010 Teratoma 52 0.033
744
THL018 Thalassemia Major 48 0.033
745
ART008 Arteriosclerosis Obliterans 42 0.033
746
CHR466 Chronic Thromboembolic Pulmonary Hypertension 39 0.033
747
DXR001 Doxorubicin Induced Cardiomyopathy 37 0.033
748
MTC028 Mitochondrial Cardiomyopathy 32 0.033
749
VTM003 Vitamin Metabolic Disorder 30 0.033
750
c VNT028 Ventricular Septal Defect 1 27 0.033
751
c VNT026 Ventricular Septal Defect 2 23 0.033
752
ADN018 Adenoma 58 0.033
753
INT253 Intestinal Benign Neoplasm 47 0.033
754
PNC065 Pinched Nerve 10 0.033
755
P CSH001 Cushing's Syndrome 65 0.033
756
SPT004 Septic Arthritis 60 0.033
757
c HPT007 Hepatitis E 54 0.033
758
ACH005 Achalasia 52 0.033
759
GTR002 Goiter 52 0.033
760
INT075 Intracranial Hypertension 50 0.033
761
P KLP003 Klippel-Feil Syndrome 46 0.033
762
P PSR002 Psoriasis 61 0.033
763
P HMP007 Hemophilia 57 0.033
764
INT002 Intermittent Claudication 56 0.033
765
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.033
766
BRN004 Brain Edema 52 0.033
767
CRS005 Crest Syndrome 51 0.033
768
PRS045 Prostatic Hypertrophy 45 0.033
769
DFF003 Diffuse Scleroderma 41 0.033
770
SCR015 Scarlet Fever 38 0.033
771
MYT026 Myotonia Atrophica 18 0.033
772
MLT131 Multifocal Atrial Tachycardia 16 0.033
773
ATR076 Atrophic Muscular Disease 15 0.033
774
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.032
775
P BPL003 Bipolar Disorder 62 0.032
776
MTN003 Motion Sickness 48 0.032
777
DVL001 Developmental Coordination Disorder 36 0.032
778
c CNG148 Congenital Heart Disease, Atrial Septal Defect 18 0.032
779
LMY002 Leiomyoma 54 0.032
780
NRP015 Neuropathy, Congenital Hypomyelinating 52 0.032
781
DBT062 Diabetic Foot Ulcers 51 0.032
782
P HRD018 Hair Disease 51 0.032
783
RSS002 Roussy-Levy Syndrome 50 0.032
784
c CLL013 Cell Type Cancer 46 0.032
785
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 43 0.032
786
FTD001 Foot Drop 33 0.032
787
DSS010 Dissociative Disorder 32 0.032
788
CRB040 Cerebrum Cancer 32 0.032
789
c CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 30 0.032
790
P LPR003 Leprosy 69 0.032
791
P PRT013 Portal Hypertension 60 0.032
792
PRM042 Primary Effusion Lymphoma 53 0.032
793
RTN018 Retinal Disease 53 0.032
794
CRV043 Cervical Dystonia 44 0.032
795
c PRS116 Prostate Cancer 1 37 0.032
796
PHN003 Phenylketonuria 72 0.031
797
c SPN225 Spondyloarthropathy 1 62 0.031
798
P LYM033 Lymphoproliferative Syndrome 56 0.031
799
GST037 Gastroparesis 54 0.031
800
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 53 0.031
801
LYM024 Lymphatic System Disease 52 0.031
802
PLS009 Plasma Cell Neoplasm 48 0.031
803
P MTH007 Methemoglobinemia 45 0.031
804
UND005 Undifferentiated Pleomorphic Sarcoma 44 0.031
805
c BRG005 Brugada Syndrome 1 40 0.031
806
c HYP072 Hypersensitivity Reaction Type Iii Disease 38 0.031
807
c CRD199 Cardiomyopathy, Hypertrophic 6 36 0.031
808
FXF002 Fox-Fordyce Disease 36 0.031
809
MLT021 Multiple System Atrophy 70 0.031
810
TST021 Testicular Germ Cell Tumor 69 0.031
811
P OVR049 Ovarian Disease 56 0.031
812
HMF006 Hemifacial Microsomia 55 0.031
813
FML038 Female Reproductive Organ Cancer 50 0.031
814
FBR054 Fibroma 46 0.031
815
NWB001 Newborn Respiratory Distress Syndrome 45 0.031
816
c LNG053 Long Qt Syndrome 9 44 0.031
817
CHR322 Choreoathetosis, Hypothyroidism, and Neonatal Respiratory Distress 40 0.031
818
MYF002 Myofascial Pain Syndrome 39 0.031
819
MCR103 Microtia 37 0.031
820
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 33 0.031
821
c BRG006 Brugada Syndrome 2 33 0.031
822
RSP007 Respiratory Distress Syndrome, Infant 22 0.031
823
c NNT025 Neonatal Systemic Lupus Erythematosus 13 0.031
824
P HML002 Hemolytic Anemia 62 0.031
825
P PRS038 Personality Disorder 62 0.031
826
P GLY013 Glycogen Storage Disease 60 0.031
827
c PRC016 Pre-Eclampsia 56 0.031
828
PLS011 Plasmacytoma 56 0.031
829
THR004 Thrombocytosis 55 0.031
830
P PLY014 Polycystic Kidney Disease 53 0.031
831
P RNV001 Renovascular Hypertension 47 0.031
832
TRN012 Transient Global Amnesia 39 0.031
833
CHR028 Chronic Wasting Disease 34 0.031
834
c VNT024 Ventricular Septal Defect 3 25 0.031
835
c BRG009 Brugada Syndrome 7 24 0.031
836
PRM053 Primary Release Disorder of Platelets 11 0.031
837
CNG063 Congenital Cardiovascular Shunt 10 0.031
838
P PLR004 Pleuropulmonary Blastoma 65 0.031
839
P TCL004 T-Cell Leukemia 47 0.031
840
c CLR085 Colorectal Cancer 1 45 0.031
841
INT040 Intrinsic Asthma 40 0.031
842
URT037 Urethral Stricture 33 0.031
843
LNS003 Lens Disease 33 0.031
844
NRV004 Nerve Compression Syndrome 31 0.031
845
P APL001 Aplastic Anemia 75 0.030
846
P DRM010 Dermatomyositis 62 0.030
847
c VRL010 Viral Hepatitis 60 0.030
848
P ECL001 Eclampsia 54 0.030
849
SLP001 Sleeping Sickness 48 0.030
850
ARR026 Arrhythmogenic Right Ventricular Dysplasia 1 41 0.030
851
HRT003 Heart Lymphoma 30 0.030
852
RDT005 Radiation Induced Cancer 28 0.030
853
PLY125 Polycythemia Vera, Somatic 63 0.030
854
c GLY008 Glycogen Storage Disease Ii 59 0.030
855
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.030
856
TNS005 Tonsillitis 57 0.030
857
P CYS018 Cystitis 52 0.030
858
BLR001 Biliary Atresia 52 0.030
859
P PRM006 Primary Biliary Cirrhosis 51 0.030
860
RLP001 Relapsing Polychondritis 50 0.030
861
P HMC002 Homocystinuria 50 0.030
862
SRT004 Serotonin Syndrome 49 0.030
863
P MTC004 Mitochondrial Encephalomyopathy 42 0.030
864
ABR009 Abruzzo-Erickson Syndrome 38 0.030
865
INT011 Interstitial Emphysema 38 0.030
866
P ENC011 Encephalomyopathy 37 0.030
867
ADP007 Adie Pupil 34 0.030
868
CRN265 Craniofacial Malformations, Asymmetric, with Polysyndactyly and Abnormal Skin and Gut Development 33 0.030
869
THY001 Thyroid Crisis 27 0.030
870
c INF055 Infectious Myocarditis 17 0.030
871
c CHR090 Chronic Lymphocytic Leukemia 76 0.030
872
ADR016 Adrenal Cortical Carcinoma 61 0.030
873
P MLT074 Multiple Endocrine Neoplasia 56 0.030
874
c CHR095 Chronic Progressive External Ophthalmoplegia 44 0.030
875
P BRN120 Bronchus Cancer 44 0.030
876
c FML191 Familial Long Qt Syndrome 42 0.030
877
P HYP120 Hypoaldosteronism 36 0.030
878
ACL001 Acalculous Cholecystitis 35 0.030
879
GLS004 Glossopharyngeal Neuralgia 33 0.030
880
CMB002 Combat Disorder 21 0.030
881
EWN003 Ewing Sarcoma 66 0.029
882
DNG002 Dengue Hemorrhagic Fever 63 0.029
883
P LYM025 Lymphedema 61 0.029
884
INS001 Insulinoma 61 0.029
885
c LNG047 Long Qt Syndrome 2 57 0.029
886
EMB004 Embryonal Carcinoma 57 0.029
887
HTC002 Hutchinson-Gilford Progeria 57 0.029
888
HPT022 Hepatoblastoma 55 0.029
889
MCS002 Mucositis 55 0.029
890
c INF071 Inflammatory Bowel Disease 1 51 0.029
891
c LNG050 Long Qt Syndrome 5 51 0.029
892
ADR012 Adrenal Gland Disease 48 0.029
893
P THY054 Thyrotoxic Periodic Paralysis 48 0.029
894
LYM116 Lymph Node Disease 47 0.029
895
c LNG056 Long Qt Syndrome 12 45 0.029
896
P MNN007 Meningocele 36 0.029
897
VNT001 Ventilation Pneumonitis 35 0.029
898
P ANT001 Anterolateral Myocardial Infarction 29 0.029
899
WRT002 Writing Disorder 27 0.029
900
c ADL080 Adult Acute Respiratory Distress Syndrome 19 0.029
901
GRB002 Gerbode Defect 15 0.029
902
DGT004 Digitalis Poisoning 11 0.029
903
APP008 Appendicitis 60 0.029
904
TXC002 Toxic Encephalopathy 51 0.029
905
ALL009 Allergic Conjunctivitis 51 0.029
906
BRC011 Brachial Plexus Neuropathy 36 0.029
907
c BRN108 Branchiootic Syndrome 1 34 0.029
908
SWL001 Swallowing Disorders 33 0.029
909
CRV069 Cervix Disease 32 0.029
910
END080 Endometrial Disease 27 0.029
911
HRN022 Hearing Loss/deafness 26 0.029
912
CNG059 Congenital Arteriovenous Shunt 9 0.029
913
NRL016 Neural Tube Defects 76 0.029
914
ATT013 Attention Deficit-Hyperactivity Disorder 69 0.029
915
SMT004 Smith-Lemli-Opitz Syndrome 66 0.029
916
LPT001 Leptospirosis 62 0.029
917
P NRC002 Narcolepsy 62 0.029
918
STT001 Status Epilepticus 59 0.029
919
PRT014 Protein S Deficiency 53 0.029
920
HYP080 Hypogonadism 53 0.029
921
P SYP003 Syphilis 53 0.029
922
P HML001 Hemolytic-Uremic Syndrome 51 0.029
923
ESP020 Esophageal Atresia 50 0.029
924
NNL002 Nonalcoholic Steatohepatitis 50 0.029
925
ANR004 Anuria 45 0.029
926
c HMG003 Hemoglobin E Disease 44 0.029
927
IMP006 Impulse Control Disorder 40 0.029
928
HNS001 Hansen's Disease 30 0.029
929
STR029 Sternal Cleft 18 0.029
930
ABS016 Absence of the Pulmonary Artery 17 0.029
931
P ALZ034 Alzheimer Disease 92 0.028
932
P HYD006 Hydrocephalus 66 0.028
933
P CRN037 Craniosynostosis 66 0.028
934
CRY002 Cryptorchidism 60 0.028
935
P ORL007 Oral Cavity Cancer 59 0.028
936
P UVT001 Uveitis 58 0.028
937
ORL011 Oral Cancer 56 0.028
938
FCL012 Facial Paralysis 50 0.028
939
c LNG051 Long Qt Syndrome 6 49 0.028
940
CHL061 Childhood Leukemia 49 0.028
941
BCT015 Bacteremia 48 0.028
942
AMN002 Amino Acid Metabolic Disorder 47 0.028
943
PYL006 Pyloric Stenosis 46 0.028
944
c LNG057 Long Qt Syndrome 13 44 0.028
945
FBR032 Fibromuscular Dysplasia 43 0.028
946
CRN041 Carnitine-Acylcarnitine Translocase Deficiency 43 0.028
947
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 42 0.028
948
c BRG007 Brugada Syndrome 5 39 0.028
949
OCL010 Ocular Hypotension 38 0.028
950
c SYS038 Systemic Lupus Erythematosus 2 27 0.028
951
WLD005 Wild Type Attr Amyloidosis 22 0.028
952
MYL009 Myelodysplastic Syndrome 73 0.027
953
P TBR001 Tuberous Sclerosis 67 0.027
954
HYP020 Hyperprolactinemia 60 0.027
955
ALP008 Alopecia 57 0.027
956
CYS005 Cysticercosis 54 0.027
957
BLM002 Bulimia Nervosa 52 0.027
958
c LNG092 Long Qt Syndrome-3 49 0.027
959
P ADM011 Adams-Oliver Syndrome 48 0.027
960
OLV002 Oliver Syndrome 43 0.027
961
MDS018 Mediastinal Cancer 36 0.027
962
GRM003 German Syndrome 22 0.027
963
FDL001 Fiedler's Myocarditis 22 0.027
964
CRT061 Cor Triatriatum Dexter 16 0.027
965
P ATX030 Ataxia-Telangiectasia 77 0.027
966
ULC004 Ulcerative Colitis 76 0.027
967
P EHL001 Ehlers-Danlos Syndrome 63 0.027
968
UTR039 Uterine Fibroid 57 0.027
969
EPD016 Epidermolysis Bullosa 57 0.027
970
NRT004 Neuritis 52 0.027
971
ASP003 Aseptic Meningitis 51 0.027
972
INN002 Inner Ear Disease 49 0.027
973
ACH037 Achalasia-Addisonianism-Alacrimia Syndrome 45 0.027
974
PRN011 Pernicious Anemia 44 0.027
975
TRC023 Trichinosis 42 0.027
976
P AXN001 Axonal Neuropathy 38 0.027
977
RTR001 Retrograde Amnesia 37 0.027
978
UND007 Undifferentiated Connective Tissue Disease 30 0.027
979
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 28 0.027
980
CNT067 Central Cord Syndrome 23 0.027
981
MLG026 Male Genital Organ Vascular Disease 14 0.027
982
ALL003 Allergic Rhinitis 63 0.027
983
P LNG064 Lung Cancer Susceptibility 3 62 0.027
984
GST092 Gastroesophageal Reflux 62 0.027
985
P SNS014 Sinusitis 60 0.027
986
CMM005 Common Cold 59 0.027
987
LNG039 Lung Squamous Cell Carcinoma 54 0.027
988
P LTR001 Lateral Sclerosis 53 0.027
989
CRT017 Cartilage Disease 45 0.027
990
CRP017 Carpal Tunnel Syndrome, Familial 43 0.027
991
SPR024 Supratentorial Cancer 33 0.027
992
INT053 Intracranial Vasospasm 28 0.027
993
MDN002 Median Neuropathy 28 0.027
994
FNC005 Functional Colonic Disease 27 0.027
995
c ATM007 Autoimmune Disease of Central Nervous System 25 0.027
996
ULC005 Ulcer of Lower Limbs 20 0.027
997
PLY039 Polymorphic Reticulosis 19 0.027
998
OVR077 Overuse Syndrome 17 0.027
999
LGD001 Leg Dermatosis 16 0.027
1000
c GLL026 Gallbladder Disease 3 16 0.027
1001
RPT005 Repetitive Motion Disorders 15 0.027
1002
P HMP002 Hemophagocytic Lymphohistiocytosis 64 0.026
1003
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 62 0.026
1004
CNT047 Contact Dermatitis 61 0.026
1005
P CDS001 Cadasil 55 0.026
1006
FRB001 Farber Lipogranulomatosis 53 0.026
1007
LYM019 Lymphosarcoma 53 0.026
1008
RYS001 Reye Syndrome 52 0.026
1009
P OVR046 Ovarian Cyst 51 0.026
1010
BNM001 Bone Marrow Cancer 51 0.026
1011
P CTN015 Cutaneous T Cell Lymphoma 50 0.026
1012
P SJG001 Sjogren's Syndrome 50 0.026
1013
CCN001 Cocaine Dependence 49 0.026
1014
NNN026 Noonan Syndrome with Multiple Lentigines 48 0.026
1015
HMG002 Hemoglobinuria 48 0.026
1016
CVR006 Cavernous Hemangioma 46 0.026
1017
CRY004 Cryoglobulinemia 46 0.026
1018
SPS007 Spastic Cerebral Palsy 44 0.026
1019
c LNG098 Long Qt Syndrome 14 44 0.026
1020
PLR006 Pleural Cancer 44 0.026
1021
VGN023 Vaginitis 42 0.026
1022
MNN021 Meningococcemia 39 0.026
1023
P CNT036 Central Nervous System Germ Cell Tumor 37 0.026
1024
CLD014 Cole Disease 37 0.026
1025
OCL011 Ocular Motility Disease 37 0.026
1026
GRM001 Germ Cell and Embryonal Cancer 36 0.026
1027
c SYS043 Systemic Lupus Erythematosus 1 33 0.026
1028
FNC006 Functional Gastric Disease 32 0.026
1029
P CNT044 Central Nervous System Primitive Neuroectodermal Neoplasm 30 0.026
1030
MTR031 Motor Neuro-Ophthalmic Disorders 19 0.026
1031
CYN003 Cyanide Poisoning 18 0.026
1032
c ADL022 Adult Central Nervous System Primitive Neuroectodermal Neoplasm 15 0.026
1033
EXT058 Extrasystoles, Multiform Ventricular, with Short Stature, Hyperpigmentation and Microcephaly 13 0.026
1034
MSC030 Muscular Fibrosis Multifocal Obstructed Vessels 10 0.026
1035
P OST005 Osteogenesis Imperfecta 69 0.026
1036
OTT002 Otitis Media 66 0.026
1037
P SCL018 Scoliosis 55 0.026
1038
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 54 0.026
1039
IMP002 Imperforate Anus 52 0.026
1040
P PYL005 Pyelonephritis 52 0.026
1041
PMS001 Poems Syndrome 52 0.026
1042
BRN056 Bronchopulmonary Dysplasia 48 0.026
1043
c CNG027 Congenital Hemolytic Anemia 48 0.026
1044
P HMR005 Hemorrhoid 47 0.026
1045
PLY012 Polyhydramnios 47 0.026
1046
HYP043 Hyperandrogenism 47 0.026
1047
RSP002 Respiratory Syncytial Virus Infectious Disease 46 0.026
1048
SKL014 Skeletal Dysplasia 46 0.026
1049
SKL017 Skeletal Dysplasias 45 0.026
1050
HPT020 Hepatic Vascular Disease 42 0.026
1051
HMT018 Hematopoietic Stem Cell Transplantation 41 0.026
1052
LCH001 Leech Infestation 40 0.026
1053
PRS023