Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Congenital heart block |
Is a |
False |
Congenital anomaly of myocardium |
Inferred relationship |
Some |
|
Endocardial fibroelastosis unassociated with other cardiac abnormalities. |
Is a |
False |
Congenital anomaly of myocardium |
Inferred relationship |
Some |
|
Congenital stenosis of mitral valve |
Is a |
False |
Congenital anomaly of myocardium |
Inferred relationship |
Some |
|
Congenital absence of papillary muscle |
Is a |
False |
Congenital anomaly of myocardium |
Inferred relationship |
Some |
|
Anomalous cardiac muscle bands |
Is a |
True |
Congenital anomaly of myocardium |
Inferred relationship |
Some |
|
Parachute malformation of tricuspid valve |
Is a |
False |
Congenital anomaly of myocardium |
Inferred relationship |
Some |
|
Fused mitral papillary muscles |
Is a |
True |
Congenital anomaly of myocardium |
Inferred relationship |
Some |
|
Hypoplastic mitral papillary muscle |
Is a |
False |
Congenital anomaly of myocardium |
Inferred relationship |
Some |
|
Congenital absence of right atrioventricular valve papillary muscle (disorder) |
Is a |
False |
Congenital anomaly of myocardium |
Inferred relationship |
Some |
|
Congenital fusion of right atrioventricular valve papillary muscles |
Is a |
False |
Congenital anomaly of myocardium |
Inferred relationship |
Some |
|
Primary endocardial fibroelastosis of left ventricle |
Is a |
False |
Congenital anomaly of myocardium |
Inferred relationship |
Some |
|
Congenital supravalvular mitral stenosis |
Is a |
False |
Congenital anomaly of myocardium |
Inferred relationship |
Some |
|
Hypoplasia of trabecular portion of right ventricle (disorder) |
Is a |
True |
Congenital anomaly of myocardium |
Inferred relationship |
Some |
|
Congenital abnormality of tricuspid papillary muscle (disorder) |
Is a |
True |
Congenital anomaly of myocardium |
Inferred relationship |
Some |
|
Congenital abnormality of atrioventricular valve papillary muscle in atrioventricular septal defect (disorder) |
Is a |
False |
Congenital anomaly of myocardium |
Inferred relationship |
Some |
|
Congenital abnormality of right atrioventricular valve papillary muscle in double inlet ventricle (disorder) |
Is a |
False |
Congenital anomaly of myocardium |
Inferred relationship |
Some |
|
Hypoplasia of trabecular portion of left ventricle (disorder) |
Is a |
True |
Congenital anomaly of myocardium |
Inferred relationship |
Some |
|
Absent mitral papillary muscle |
Is a |
True |
Congenital anomaly of myocardium |
Inferred relationship |
Some |
|
Uhl's disease |
Is a |
True |
Congenital anomaly of myocardium |
Inferred relationship |
Some |
|
Cardiomyopathy and renal anomaly syndrome (disorder) |
Is a |
True |
Congenital anomaly of myocardium |
Inferred relationship |
Some |
|
Cardiomyopathy-hypotonia-lactic acidosis syndrome is characterized by hypertrophic cardiomyopathy, muscular hypotonia and the presence of lactic acidosis at birth. It has been described in two sisters (both of whom died within the first year of life) from a nonconsanguineous Turkish family. The syndrome is caused by a homozygous point mutation in the exon 3A of the SLC25A3 gene encoding a mitochondrial membrane transporter. |
Is a |
True |
Congenital anomaly of myocardium |
Inferred relationship |
Some |
|
A rare autosomal dominant form of heart-hand syndrome that is characterized by adult onset, progressive cardiac conduction disease, tachyarrhythmias that can lead to sudden death, dilated cardiomyopathy and brachydactyly, with the hands less severely affected than the feet. Muscle weakness and/or myopathic electromyographic findings have been observed in some cases. |
Is a |
True |
Congenital anomaly of myocardium |
Inferred relationship |
Some |
|
Congenital cataract - hypertrophic cardiomyopathy - mitochondrial myopathy (CCM) is a mitochondrial disease characterized by cataracts, hypertrophic cardiomyopathy, muscle weakness and lactic acidosis after exercise. |
Is a |
True |
Congenital anomaly of myocardium |
Inferred relationship |
Some |
|
A rare arrhythmogenic right ventricular cardiomyopathy (ARVC) and a cutaneous phenotype, characterized by peculiar wooly hair and palmoplantar keratoderma. |
Is a |
True |
Congenital anomaly of myocardium |
Inferred relationship |
Some |
|
This syndrome is characterized by the association of dilated cardiomyopathy and hypergonadotropic hypogonadism (DCM-HH). |
Is a |
True |
Congenital anomaly of myocardium |
Inferred relationship |
Some |
|
A rare glycogen storage disease characterized by fetal or neonatal onset of severe cardiomyopathy with non-lysosomal glycogen accumulation and fatal outcome in infancy. Patients present with massive cardiomegaly, severe cardiac and respiratory complications, and failure to thrive. Non-specific facial dysmorphism, bilateral cataracts, macroglossia, hydrocephalus, enlarged kidneys, and skeletal muscle involvement have been reported in some cases. |
Is a |
True |
Congenital anomaly of myocardium |
Inferred relationship |
Some |
|