Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Congenital anomaly of cardiovascular system |
Is a |
True |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Rubella myocarditis (disorder) |
Is a |
True |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital stenosis of cardiac valve |
Is a |
False |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital cardiac failure (disorder) |
Is a |
True |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital His bundle tachycardia |
Is a |
True |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital peripheral aneurysm |
Is a |
False |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital conduction defect |
Is a |
True |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital vascular disorder |
Is a |
True |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Fenestrated interatrial communication within oval fossa (disorder) |
Is a |
False |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital stenosis of mitral subvalvular apparatus |
Is a |
False |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital pericardial effusion (disorder) |
Is a |
False |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome (disorder) |
Is a |
False |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) |
Is a |
False |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
This syndrome is characterized by the association of dilated cardiomyopathy and hypergonadotropic hypogonadism (DCM-HH). |
Is a |
False |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Cardiomyopathy and renal anomaly syndrome (disorder) |
Is a |
False |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Heart-hand syndrome Slovenian type (disorder) |
Is a |
False |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hydrocephalus with endocardial fibroelastosis and cataract syndrome (disorder) |
Is a |
False |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Glycogen storage disease due to muscle and heart glycogen synthase deficiency is characterized by muscle and heart glycogen deficiency. It has been described in three siblings (two brothers and their younger sister). The older brother died at 10.5 years of age as a result of sudden cardiac arrest and the younger brother presented with hypertrophic cardiomyopathy, abnormal heart rate and blood pressure during exercise, and muscle fatigability. The sister showed no symptoms but a lack of glycogen was identified through muscle biopsy. The syndrome is caused by homozygous missense mutations in the gene encoding muscle glycogen synthase. |
Is a |
False |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Long thumb brachydactyly syndrome (disorder) |
Is a |
True |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Carney complex (disorder) |
Is a |
False |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital anomaly of atrioventricular valve |
Is a |
True |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital anomaly of atrioventricular septum |
Is a |
False |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome |
Is a |
False |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Ankyrin-B syndrome |
Is a |
True |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Carney complex, trismus, pseudocamptodactyly syndrome (disorder) |
Is a |
True |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital septal defect of heart |
Is a |
False |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Sinoatrial node dysfunction and deafness (disorder) |
Is a |
True |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Extrasystoles, short stature, hyperpigmentation, microcephaly syndrome |
Is a |
True |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency |
Is a |
True |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Patent foramen ovale |
Is a |
False |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Cyanotic congenital heart disease |
Is a |
False |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Tripartite right ventricle |
Is a |
True |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Posterior deviation of infundibular septum of obstructive aortic arch type (disorder) |
Is a |
False |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Autosomal recessive leukoencephalopathy, ischemic stroke, retinitis pigmentosa syndrome (disorder) |
Is a |
True |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Timothy syndrome type 1 |
Is a |
False |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Timothy syndrome type 2 (disorder) |
Is a |
False |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Familial long QT syndrome |
Is a |
False |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital dysplasia of truncal valve |
Is a |
False |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital hypoplasia of anulus fibrosus of aorta |
Is a |
False |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Late congenital cardiovascular syphilis |
Is a |
True |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Endocardial fibroelastosis of right atrium |
Is a |
True |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Endocardial fibroelastosis of left atrium (disorder) |
Is a |
True |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Cardiac glycogenosis (disorder) |
Is a |
True |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital rhabdomyoma of heart |
Is a |
True |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Eye defects, arachnodactyly, cardiopathy syndrome |
Is a |
True |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Timothy syndrome |
Is a |
True |
Congenital cardiovascular disorder (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|