Tetralogy of Fallot
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Congenital Abnormality
|
274
|
83
|
0.960 |
None |
0.909 |
11 |
6
|
1999 |
2018 |
Hypoplastic Left Heart Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
52
|
7
|
0.810 |
None |
1.000 |
4 |
|
2003 |
2017 |
ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS
|
disease |
|
Disease or Syndrome
|
1
|
31
|
0.800 |
None |
1.000 |
7 |
31
|
1998 |
2017 |
Atrial Septal Defect with Atrioventricular Conduction Defects
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
1
|
1
|
0.700 |
strong |
1.000 |
3 |
1
|
2008 |
2017 |
CONOTRUNCAL HEART MALFORMATIONS (disorder)
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
13
|
22
|
0.600 |
None |
1.000 |
3 |
1
|
2003 |
2012 |
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 5 (disorder)
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
1
|
3
|
0.600 |
None |
1.000 |
1 |
3
|
2006 |
2006 |
HYPOPLASTIC LEFT HEART SYNDROME 2
|
disease |
|
Disease or Syndrome
|
8
|
11
|
0.500 |
None |
1.000 |
2 |
1
|
2003 |
2005 |
VENTRICULAR SEPTAL DEFECT 3
|
disease |
|
Disease or Syndrome; Congenital Abnormality
|
1
|
2
|
0.500 |
moderate |
1.000 |
2 |
2
|
2010 |
2011 |
Ventricular Septal Defects
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Congenital Abnormality
|
426
|
87
|
0.490 |
None |
1.000 |
9 |
5
|
2005 |
2017 |
Atrial Fibrillation
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
939
|
584
|
0.460 |
None |
0.889 |
9 |
2
|
2006 |
2019 |
Ostium secundum atrial septal defect
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Congenital Abnormality
|
37
|
10
|
0.430 |
None |
1.000 |
5 |
|
2003 |
2017 |
Bicuspid aortic valve
|
disease |
Cardiovascular Diseases
|
Congenital Abnormality
|
154
|
23
|
0.420 |
None |
1.000 |
3 |
1
|
2006 |
2016 |
Heart Septal Defects
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Congenital Abnormality
|
77
|
12
|
0.420 |
strong |
0.500 |
2 |
1
|
2009 |
2019 |
Atrial Septal Defects
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Congenital Abnormality
|
384
|
96
|
0.400 |
None |
1.000 |
15 |
8
|
2002 |
2019 |
Aortic valve calcification
|
disease |
Nutritional and Metabolic Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
79
|
4
|
0.400 |
None |
1.000 |
1 |
|
2014 |
2014 |
Thyroid Agenesis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases
|
Congenital Abnormality
|
11
|
3
|
0.400 |
None |
1.000 |
1 |
|
2006 |
2006 |
Ectopic thyroid tissue (disorder)
|
phenotype |
|
Disease or Syndrome
|
8
|
1
|
0.400 |
None |
1.000 |
1 |
|
2006 |
2006 |
Cardiomyopathy, Familial Idiopathic
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
773
|
243
|
0.330 |
None |
1.000 |
4 |
1
|
2015 |
2017 |
Foramen Ovale, Patent
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Congenital Abnormality
|
73
|
14
|
0.330 |
None |
1.000 |
4 |
|
2003 |
2017 |
Cerebrovascular accident
|
group |
Nervous System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
1658
|
591
|
0.310 |
None |
1.000 |
2 |
1
|
2009 |
2018 |
Cardiomyopathy, Dilated
|
group |
Cardiovascular Diseases
|
Disease or Syndrome
|
512
|
509
|
0.310 |
None |
1.000 |
2 |
1
|
2017 |
2017 |
Myotonic Dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
155
|
4
|
0.310 |
None |
1.000 |
1 |
|
2008 |
2008 |
Splenic Hypoplasia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases
|
Congenital Abnormality
|
18
|
9
|
0.310 |
None |
1.000 |
1 |
|
2012 |
2012 |
Paroxysmal atrial fibrillation
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
226
|
8
|
0.300 |
None |
1.000 |
3 |
|
2010 |
2018 |
Persistent atrial fibrillation
|
phenotype |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Pathologic Function
|
156
|
|
0.300 |
None |
1.000 |
3 |
|
2010 |
2018 |