Brugada Syndrome (disorder)
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
3
|
103
|
1.000 |
definitive |
0.984 |
162 |
101
|
1995 |
2020 |
LONG QT SYNDROME 3
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
1
|
30
|
1.000 |
None |
1.000 |
21 |
30
|
1995 |
2018 |
Hereditary bundle branch system defect
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
2
|
7
|
0.980 |
None |
1.000 |
0 |
6
|
1995 |
2013 |
Brugada Syndrome 1
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
1
|
34
|
0.910 |
None |
1.000 |
8 |
34
|
1995 |
2018 |
CARDIOMYOPATHY, DILATED, 1E
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
1
|
11
|
0.900 |
None |
1.000 |
0 |
11
|
1995 |
2017 |
Ventricular Fibrillation, Paroxysmal Familial, 1
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
1
|
3
|
0.800 |
None |
0.833 |
0 |
3
|
1995 |
2018 |
Sudden infant death syndrome
|
disease |
Pathological Conditions, Signs and Symptoms
|
Disease or Syndrome
|
2
|
5
|
0.800 |
None |
0.963 |
0 |
4
|
1995 |
2018 |
SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
1
|
8
|
0.710 |
None |
1.000 |
0 |
8
|
1995 |
2012 |
Cardiomyopathy, Dilated
|
group |
Cardiovascular Diseases
|
Disease or Syndrome
|
43
|
443
|
0.700 |
strong |
1.000 |
16 |
3
|
1998 |
2018 |
Long QT Syndrome
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
16
|
245
|
0.700 |
strong |
0.987 |
3 |
4
|
1995 |
2020 |
Paroxysmal familial ventricular fibrillation
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
3
|
3
|
0.700 |
moderate |
1.000 |
0 |
1
|
2000 |
2016 |
ATRIAL FIBRILLATION, FAMILIAL, 10
|
disease |
|
Disease or Syndrome
|
1
|
9
|
0.700 |
None |
1.000 |
0 |
9
|
1995 |
2012 |
Atrial Fibrillation
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
2
|
2
|
0.500 |
None |
1.000 |
0 |
1
|
2005 |
2019 |
Sick Sinus Syndrome
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
1
|
1
|
0.480 |
None |
1.000 |
0 |
1
|
2005 |
2018 |
Familial dilated cardiomyopathy
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
10
|
32
|
0.430 |
None |
1.000 |
0 |
2
|
2004 |
2018 |
Romano-Ward Syndrome
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
5
|
15
|
0.410 |
None |
1.000 |
6 |
4
|
1999 |
2013 |
Sinus Node Dysfunction (disorder)
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
1
|
1
|
0.400 |
None |
1.000 |
0 |
1
|
2005 |
2019 |
LONG QT SYNDROME 2/3, DIGENIC
|
disease |
|
Disease or Syndrome
|
2
|
2
|
0.300 |
None |
1.000 |
0 |
1
|
2001 |
2012 |
LONG QT SYNDROME 3/6, DIGENIC Disorder
|
disease |
|
Disease or Syndrome
|
2
|
2
|
0.300 |
None |
1.000 |
0 |
1
|
2001 |
2012 |
Cardiac Conduction Defect, Nonprogressive
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
1
|
1
|
0.300 |
None |
1.000 |
0 |
1
|
2002 |
2011 |
Heart Block, Nonprogressive
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
1
|
1
|
0.300 |
None |
1.000 |
0 |
1
|
2002 |
2011 |
CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder)
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
3
|
4
|
0.300 |
None |
1.000 |
0 |
1
|
2005 |
2011 |
LONG QT SYNDROME 3, ACQUIRED, SUSCEPTIBILITY TO (finding)
|
disease |
|
Finding
|
1
|
1
|
0.300 |
None |
1.000 |
0 |
1
|
2001 |
2012 |
Congenital long QT syndrome
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
5
|
21
|
0.200 |
None |
1.000 |
8 |
3
|
1996 |
2018 |
Syncope
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Sign or Symptom
|
8
|
12
|
0.170 |
None |
1.000 |
0 |
1
|
2002 |
2019 |