Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Implantation of blood vessels into myocardium |
Procedure site - Indirect (attribute) |
True |
Myocardium structure |
Inferred relationship |
Some |
2 |
Aorto-myocardial shunt |
Procedure site - Indirect (attribute) |
False |
Myocardium structure |
Inferred relationship |
Some |
4 |
Erythrokeratodermia-cardiomyopathy syndrome is a rare, genetic erythrokeratoderma disorder characterized by generalized cutaneous erythema with fine white scales and pruritus refractory to treatment, progressive dilated cardiomyopathy, palmoplantar keratoderma, sparse or absent eyebrows and eyelashes, sparse scalp hair, nail dystrophy, and dental enamel anomalies. Variable features include failure to thrive, developmental delay, and development of corneal opacities. Histology shows psoriasiform acanthosis, hypogranulosis, and compact orthohyperkeratosis. |
Finding site |
True |
Myocardium structure |
Inferred relationship |
Some |
1 |
A rare mitochondrial disease characterized by neonatal onset of severe cardiac and/or neurologic signs and symptoms mostly associated with a fatal outcome in the neonatal period or in infancy, although a milder phenotype with later onset and slowly progressive neurologic deterioration has also been reported. Clinical manifestations are variable and include respiratory insufficiency, hypotonia, cardiomyopathy, and seizures. Serum lactate is elevated in most cases. Brain imaging may show cerebellar atrophy or hypoplasia. |
Finding site |
True |
Myocardium structure |
Inferred relationship |
Some |
1 |
Cardiomyopathy due to acromegaly (disorder) |
Finding site |
True |
Myocardium structure |
Inferred relationship |
Some |
1 |
Maternally inherited mitochondrial cardiomyopathy (disorder) |
Finding site |
True |
Myocardium structure |
Inferred relationship |
Some |
1 |
A rare mitochondrial disease characterized by prenatal or early infantile onset of severe cardiomyopathy, failure to thrive and global developmental delay, sensorineural hearing loss, and severe lactic acidosis. Hepatic involvement and adrenal insufficiency, as well as encephalopathy and anomalies of deep gray matter structures on brain MRI have also been reported. |
Finding site |
True |
Myocardium structure |
Inferred relationship |
Some |
1 |
Myocardial dysfunction with sepsis (disorder) |
Finding site |
True |
Myocardium structure |
Inferred relationship |
Some |
2 |
Subsequent anterior non-ST segment elevation myocardial infarction (disorder) |
Finding site |
True |
Myocardium structure |
Inferred relationship |
Some |
3 |
Myocarditis due to idiopathic hypereosinophilic syndrome |
Finding site |
True |
Myocardium structure |
Inferred relationship |
Some |
1 |
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. |
Finding site |
True |
Myocardium structure |
Inferred relationship |
Some |
1 |
Dilated cardiomyopathy caused by ethanol (disorder) |
Finding site |
True |
Myocardium structure |
Inferred relationship |
Some |
1 |
Replacement of electronic heart device, myocardial electrode |
Procedure site - Indirect (attribute) |
True |
Myocardium structure |
Inferred relationship |
Some |
1 |
Dilated cardiomyopathy due to scleroderma (disorder) |
Finding site |
True |
Myocardium structure |
Inferred relationship |
Some |
1 |
Acute ST segment elevation myocardial infarction due to occlusion of proximal portion of circumflex branch of left coronary artery (disorder) |
Finding site |
True |
Myocardium structure |
Inferred relationship |
Some |
1 |
Acute ST segment elevation myocardial infarction due to distal left circumflex coronary artery occlusion |
Finding site |
True |
Myocardium structure |
Inferred relationship |
Some |
1 |
Acute ST segment elevation myocardial infarction due to obtuse marginal branch of left circumflex coronary artery occlusion |
Finding site |
True |
Myocardium structure |
Inferred relationship |
Some |
1 |
Acute ST segment elevation myocardial infarction due to posterolateral branch of left circumflex coronary artery occlusion |
Finding site |
True |
Myocardium structure |
Inferred relationship |
Some |
1 |
Acute ST segment elevation myocardial infarction due to mid left circumflex coronary artery occlusion |
Finding site |
True |
Myocardium structure |
Inferred relationship |
Some |
1 |
A rare inborn error of metabolism characterized by massive accumulation of triglycerides in the myocardium and coronary arteries, while plasma triglyceride levels are normal. Patients present in adulthood with signs and symptoms of coronary artery disease and severe heart failure. Concomitant skeletal myopathy is common. Vacuole formation in polymorphonuclear leukocytes is typically observed. |
Finding site |
True |
Myocardium structure |
Inferred relationship |
Some |
2 |
Toxic dilated cardiomyopathy (disorder) |
Finding site |
True |
Myocardium structure |
Inferred relationship |
Some |
1 |
Toxic cardiomyopathy |
Finding site |
True |
Myocardium structure |
Inferred relationship |
Some |
1 |
Transient myocardial ischaemia |
Finding site |
True |
Myocardium structure |
Inferred relationship |
Some |
1 |
Prinzmetal angina |
Finding site |
True |
Myocardium structure |
Inferred relationship |
Some |
1 |
Aorto-myocardial shunt |
Procedure site - Direct (attribute) |
True |
Myocardium structure |
Inferred relationship |
Some |
2 |
Structure of myocardium of apex of heart |
Is a |
True |
Myocardium structure |
Inferred relationship |
Some |
|
Type 5 myocardial infarction (disorder) |
Finding site |
True |
Myocardium structure |
Inferred relationship |
Some |
1 |
Structure of myocardium of cardiac septum |
Is a |
True |
Myocardium structure |
Inferred relationship |
Some |
|
Eosinophil infiltration of myocardium (finding) |
Finding site |
True |
Myocardium structure |
Inferred relationship |
Some |
1 |
An early-onset and most severe form of rare haemochromatosis characterised by the usual features of haemochromatosis accompanied by cardiomyopathy and hypogonadism. |
Finding site |
True |
Myocardium structure |
Inferred relationship |
Some |
3 |
Type 2A juvenile hereditary hemochromatosis (disorder) |
Finding site |
True |
Myocardium structure |
Inferred relationship |
Some |
3 |
Type 2B juvenile hereditary hemochromatosis |
Finding site |
True |
Myocardium structure |
Inferred relationship |
Some |
3 |
Angina pectoris due to microvascular ischemia of myocardium (disorder) |
Finding site |
True |
Myocardium structure |
Inferred relationship |
Some |
1 |
Acute microvascular ischemia of myocardium |
Finding site |
True |
Myocardium structure |
Inferred relationship |
Some |
1 |
Angina pectoris due to arteriosclerosis of nonautologous biological coronary artery bypass graft (disorder) |
Finding site |
True |
Myocardium structure |
Inferred relationship |
Some |
2 |
Myocardial ischemia due to coronary arteriosclerosis |
Finding site |
True |
Myocardium structure |
Inferred relationship |
Some |
1 |
Chronic microvascular ischemia of myocardium (disorder) |
Finding site |
True |
Myocardium structure |
Inferred relationship |
Some |
1 |