Cardiomyopathy, Familial Hypertrophic, 2
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
1
|
30
|
0.900 |
strong |
1.000 |
96 |
30
|
1991 |
2019 |
CARDIOMYOPATHY, DILATED, 1D (disorder)
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
1
|
24
|
0.900 |
strong |
1.000 |
95 |
24
|
1991 |
2019 |
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
1
|
21
|
0.600 |
strong |
1.000 |
93 |
21
|
1991 |
2019 |
Adult Glycogen Storage Disease Type II
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
2
|
|
0.300 |
None |
1.000 |
1 |
|
2016 |
2016 |
Glycogen Storage Disease Type II, Juvenile
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
2
|
|
0.300 |
None |
1.000 |
1 |
|
2016 |
2016 |
Progressive Familial Heart Block, Type II
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
2
|
|
0.010 |
None |
1.000 |
1 |
|
2005 |
2005 |
Glycogen Storage Disease Type II, Infantile
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
4
|
4
|
0.300 |
None |
1.000 |
1 |
|
2016 |
2016 |
Other restrictive cardiomyopathy
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
5
|
|
0.300 |
None |
1.000 |
1 |
|
2006 |
2006 |
Obstructive asymmetric septal hypertrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
7
|
|
0.300 |
None |
1.000 |
2 |
|
1997 |
2003 |
Idiopathic hypertrophic subaortic stenosis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Congenital Abnormality
|
7
|
|
0.300 |
None |
1.000 |
2 |
|
1997 |
2003 |
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
9
|
163
|
0.100 |
None |
1.000 |
8 |
1
|
1997 |
2015 |
Cardiac troponin T measurement
|
phenotype |
|
Laboratory Procedure
|
11
|
19
|
0.100 |
None |
1.000 |
1 |
2
|
2013 |
2013 |
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
21
|
24
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Sudden Cardiac Arrest
|
phenotype |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Pathologic Function
|
27
|
32
|
0.300 |
None |
1.000 |
1 |
|
2007 |
2007 |
Sudden death
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Pathologic Function
|
30
|
3
|
0.100 |
None |
|
0 |
|
|
|
Left ventricular noncompaction
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
35
|
26
|
0.310 |
None |
1.000 |
2 |
|
2009 |
2010 |
Chronic Airflow Obstruction
|
disease |
Respiratory Tract Diseases
|
Disease or Syndrome
|
35
|
|
0.300 |
None |
1.000 |
1 |
|
2007 |
2007 |
HYPOPLASTIC LEFT HEART SYNDROME 1
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
37
|
12
|
0.010 |
None |
1.000 |
1 |
|
2014 |
2014 |
Left ventricular noncompaction cardiomyopathy
|
disease |
Pathological Conditions, Signs and Symptoms
|
Disease or Syndrome
|
39
|
28
|
0.020 |
None |
1.000 |
2 |
1
|
2010 |
2015 |
Restrictive cardiomyopathy
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
41
|
30
|
0.110 |
None |
1.000 |
2 |
4
|
1999 |
2006 |
Conduction disorder of the heart
|
group |
Cardiovascular Diseases
|
Disease or Syndrome
|
41
|
11
|
0.010 |
None |
< 0.001 |
1 |
|
2005 |
2005 |
Wolff-Parkinson-White Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
48
|
22
|
0.100 |
None |
|
0 |
1
|
|
|
Generalized glycogen storage disease of infants
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
51
|
16
|
0.300 |
None |
1.000 |
1 |
|
2016 |
2016 |
Congenital muscular dystrophy (disorder)
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
54
|
20
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Necrosis
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Organ or Tissue Function
|
60
|
|
0.300 |
None |
1.000 |
1 |
|
2007 |
2007 |