Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
MRI of heart for myocardial viability assessment |
Procedure site - Direct (attribute) |
True |
Heart structure |
Inferred relationship |
Some |
1 |
Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome is a rare, genetic, neurodegenerative disease characterized by episodic metabolic encephalomyopathic crises (of variable frequency and severity which are frequently precipitated by an acute illness) which manifest with profound muscle weakness, ataxia, seizures, cardiac arrhythmias, rhabdomyolysis with myoglobinuria, elevated plasma creatine kinase, hypoglycemia, lactic acidosis, increased acylcarnitines and a disorientated or comatose state. Global developmental delay, intellectual disability and cortical, pyramidal and cerebellar signs develop with subsequent progressive neurodegeneration causing loss of expressive language and varying degrees of cerebral atrophy. |
Finding site |
False |
Heart structure |
Inferred relationship |
Some |
4 |
Xenotransplant of heart |
Procedure site - Direct (attribute) |
False |
Heart structure |
Inferred relationship |
Some |
1 |
Implantation of cardiac defibrillator lead (procedure) |
Procedure site - Direct (attribute) |
True |
Heart structure |
Inferred relationship |
Some |
1 |
mise en place de défibrillateur implantable biventriculaire, sous fluoroscopie |
Procedure site - Indirect (attribute) |
False |
Heart structure |
Inferred relationship |
Some |
3 |
A rare subtype of autosomal recessive limb-girdle muscular dystrophy characterized by atrioventricular block resulting in repeated syncope episodes, elevated creatine kinase serum levels and adult-onset of slowly progressive proximal limb skeletal muscle weakness and atrophy. Muscular dystrophic changes observed in muscle biopsy include diameter variability, increased central nuclei, and presence of necrotic and regenerating fibers. |
Finding site |
False |
Heart structure |
Inferred relationship |
Some |
3 |
Disorder of heart caused by Salmonella enterica subspecies enterica serovar Typhi |
Finding site |
False |
Heart structure |
Inferred relationship |
Some |
1 |
A rare genetic disease characterized by intellectual disability, developmental delay, language deficits, and cardiac arrhythmia (most commonly sick sinus syndrome). Additional reported features include epilepsy, hypotonia, retinal abnormalities, nystagmus, attention deficit hyperactivity disorder, autism, and gastroesophageal reflux. The severity of the phenotype is highly variable. |
Finding site |
False |
Heart structure |
Inferred relationship |
Some |
1 |
Abnormal heart to thorax ratio of fetus (finding) |
Finding site |
True |
Heart structure |
Inferred relationship |
Some |
1 |
Exploratory cardiotomy |
Procedure site - Direct (attribute) |
True |
Heart structure |
Inferred relationship |
Some |
2 |
A rare genetic disease characterized by early-onset respiratory difficulties and frequent respiratory infections, congenital heart defects, dysostosis multiplex, hepatosplenomegaly, renal involvement, hematopoietic abnormalities, facial dysmorphism (coarse facial features, large forehead, synophrys, long eyelashes, broad nasal bridge, macroglossia, short neck, and low hairline), and global developmental delay. Laboratory examination shows increased urinary excretion of glycosaminoglycans and increased plasma heparan sulfate, but no lysosomal enzyme deficiency. The disease is usually fatal in the first years of life. |
Finding site |
True |
Heart structure |
Inferred relationship |
Some |
2 |
Cardiac familial non-neuropathic amyloidosis |
Finding site |
True |
Heart structure |
Inferred relationship |
Some |
1 |
Localised hereditary cardiac amyloidosis |
Finding site |
True |
Heart structure |
Inferred relationship |
Some |
1 |
Doppler flow mapping of heart |
Procedure site - Direct (attribute) |
True |
Heart structure |
Inferred relationship |
Some |
1 |
Cardiac secondary systemic amyloidosis |
Finding site |
True |
Heart structure |
Inferred relationship |
Some |
1 |
Cardiac arrhythmia due to coronary artery spasm |
Finding site |
False |
Heart structure |
Inferred relationship |
Some |
1 |
Eye defects, arachnodactyly, cardiopathy syndrome |
Finding site |
True |
Heart structure |
Inferred relationship |
Some |
5 |
Long QT syndrome type 9 |
Finding site |
False |
Heart structure |
Inferred relationship |
Some |
1 |
Long QT syndrome type 6 (disorder) |
Finding site |
False |
Heart structure |
Inferred relationship |
Some |
1 |
A rare multiple congenital anomalies/dysmorphic syndrome characterized by global developmental delay or regression, variable congenital heart defects (such as patent ductus arteriosus, atrial or ventricular septal defects, and double outlet right ventricle, among others), and dysmorphic features (including ptosis, epicanthal folds, abnormally set/dysplastic ears, low hairline or excess nuchal skin, wide-spaced/inverted nipples, umbilical hernia or diastasis recti, and digital anomalies). Additional variable manifestations are hyper- or hypotonia, seizures, hearing loss, cortical blindness, and optic atrophy. Brain imaging may show cerebral and cerebellar atrophy and hydrocephalus. |
Finding site |
True |
Heart structure |
Inferred relationship |
Some |
2 |
Long QT syndrome type 11 (disorder) |
Finding site |
False |
Heart structure |
Inferred relationship |
Some |
1 |
Long QT syndrome type 10 (disorder) |
Finding site |
False |
Heart structure |
Inferred relationship |
Some |
1 |
Long QT syndrome type 3 (disorder) |
Finding site |
False |
Heart structure |
Inferred relationship |
Some |
1 |
Long QT syndrome type 12 (disorder) |
Finding site |
False |
Heart structure |
Inferred relationship |
Some |
1 |
Long QT syndrome type 13 (disorder) |
Finding site |
False |
Heart structure |
Inferred relationship |
Some |
1 |
Long QT syndrome type 4 (disorder) |
Finding site |
False |
Heart structure |
Inferred relationship |
Some |
1 |
Long QT syndrome type 5 (disorder) |
Finding site |
False |
Heart structure |
Inferred relationship |
Some |
1 |
Long QT syndrome type 2 (disorder) |
Finding site |
False |
Heart structure |
Inferred relationship |
Some |
1 |
Cardiac pacemaker battery depletion at elective replacement indicator timing alert (finding) |
Finding site |
True |
Heart structure |
Inferred relationship |
Some |
2 |
Infection of heart caused by Salmonella enterica enterica serovar Typhi |
Finding site |
True |
Heart structure |
Inferred relationship |
Some |
1 |
Biopsy of heart using fluoroscopic angiography guidance with contrast (procedure) |
Procedure site - Direct (attribute) |
True |
Heart structure |
Inferred relationship |
Some |
1 |
A rare, genetic, neurodevelopmental disorder characterized by global developmental delay, congenital heart defects, generalized hypertrichosis and dysmorphic facial features, most commonly triangular face, thick arched eyebrows, widely spaced eyes, posteriorly rotated low set ears, depressed nasal bridge, broad nasal root and tip, and pointed chin. |
Finding site |
True |
Heart structure |
Inferred relationship |
Some |
1 |
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by global developmental delay, intellectual disability, hypotonia, craniofacial dysmorphism (such as ridged metopic sutures, long palpebral fissures, broad nasal bridge, hypoplastic alae nasi, low-set, prominent ears, prominent midline tongue groove, and downturned mouth), congenital heart defects, and variable skeletal abnormalities including hip dysplasia, vertebral anomalies, and scoliosis. Additional reported manifestations include high pain tolerance and genitourinary anomalies. Brain imaging may show a thin corpus callosum or white matter abnormalities. |
Finding site |
True |
Heart structure |
Inferred relationship |
Some |
3 |
A rare genetic lethal multiple congenital anomalies/dysmorphic syndrome characterized by early intrauterine growth retardation, generalized edema, craniofacial dysmorphism (such as microcephaly, brachycephaly, frontal bossing, hypertelorism, short palpebral fissures, or absent nasal bone), cerebellar hypoplasia, sex reversal in male fetuses, congenital heart defects (including septal and valve defects and cardiomegaly), and late fetal loss. |
Finding site |
True |
Heart structure |
Inferred relationship |
Some |
1 |
A rare, multiple congenital anomalies syndrome with cardiac involvement as a major feature characterized by QT prolongation, congenital heart defects, syndactyly, facial dysmorphism and neurodevelopmental features. There are three clinical phenotypes recognized, the classical types that present with a prolonged QT interval and either with (TS1) or without (TS2) cutaneous syndactyly of fingers and toes. The atypical form (ATS) causes multi-system health concerns but not necessarily with prolonged QT. |
Finding site |
True |
Heart structure |
Inferred relationship |
Some |
2 |
A rare multiple congenital anomalies syndrome with cardiac involvement as a major feature with characteristics of QT prolongation, congenital heart defects, syndactyly, facial dysmorphism and neurodevelopmental features. The atypical form (ATS) causes multi-system health concerns but not necessarily with prolonged QT. The disease can be recognized by any CACNA1C change (excluding the G406R change) that causes multi-system health concerns. |
Finding site |
True |
Heart structure |
Inferred relationship |
Some |
2 |
A rare lethal multiple congenital anomalies/dysmorphic syndrome characterized by the association of fetal akinesia sequence, bilateral microphthalmia, microtia, and persistent truncus arteriosus. Additional dysmorphic features include prominent forehead, small nose, micrognathia, as well as camptodactyly and symphalangism. Contractures of large joints and micropenis have also been reported. |
Finding site |
True |
Heart structure |
Inferred relationship |
Some |
5 |
Postoperative cardiac arrhythmia |
Finding site |
False |
Heart structure |
Inferred relationship |
Some |
2 |
Cardiac tamponade following operative procedure (disorder) |
Finding site |
True |
Heart structure |
Inferred relationship |
Some |
1 |
Ebstein's anomaly of left sided tricuspid valve with discordant atrioventricular connections (disorder) |
Finding site |
True |
Heart structure |
Inferred relationship |
Some |
2 |
Implantation of leadless cardiac pacemaker |
Procedure site - Indirect (attribute) |
True |
Heart structure |
Inferred relationship |
Some |
1 |
Replacement of cardiac resynchronisation therapy defibrillator pulse generator |
Procedure site - Indirect (attribute) |
True |
Heart structure |
Inferred relationship |
Some |
1 |
Replacement of leadless cardiac pacemaker (procedure) |
Procedure site - Indirect (attribute) |
True |
Heart structure |
Inferred relationship |
Some |
1 |
Implantation of cardiac resynchronization defibrillator lead (procedure) |
Procedure site - Direct (attribute) |
True |
Heart structure |
Inferred relationship |
Some |
1 |
Implantation of cardiac resynchronization defibrillator system (procedure) |
Procedure site - Indirect (attribute) |
True |
Heart structure |
Inferred relationship |
Some |
1 |
Implantation of cardiac resynchronization defibrillator system (procedure) |
Procedure site - Indirect (attribute) |
False |
Heart structure |
Inferred relationship |
Some |
2 |
A rare disorder of pentose phosphate metabolism characterized by developmental delay and intellectual disability, delayed or absent speech, short stature, and congenital heart defects (such as ventricular septal defect, atrial septal defect, and patent foramen ovale). Additional reported features include hypotonia, hyperactivity, stereotypic behavior, ophthalmologic abnormalities (bilateral cataract, uveitis, strabismus), hearing impairment, and variable facial dysmorphism, among others. Laboratory analysis shows elevated plasma and urinary polyols (erythritol, arabitol, and ribitol) and urinary sugar-phosphates (ribose-5-phosphate and xylulose/ribulose-5-phosphate). |
Finding site |
True |
Heart structure |
Inferred relationship |
Some |
1 |
A rare genetic neurodevelopmental disorder characterized by global developmental delay (DD) and variable degrees of intellectual disability (ID) with delayed or limited/absent speech development associated with neonatal hypotonia, feeding difficulties, cardiac anomalies and dysmorphic facial features, predominantly broad nasal tip and thin, tented upper lip. Microcephaly, frequent infections, gastrointestinal and/or ocular anomalies have also been described. |
Finding site |
True |
Heart structure |
Inferred relationship |
Some |
1 |
Cardiac implant |
This attribute represents the site where the device is intended to reside in or on the body. |
True |
Heart structure |
Inferred relationship |
Some |
|
Temporary artificial heart prosthesis |
This attribute represents the site where the device is intended to reside in or on the body. |
True |
Heart structure |
Inferred relationship |
Some |
|
Implantable defibrillator |
This attribute represents the site where the device is intended to reside in or on the body. |
True |
Heart structure |
Inferred relationship |
Some |
|
Non-valved conduit |
This attribute represents the site where the device is intended to reside in or on the body. |
True |
Heart structure |
Inferred relationship |
Some |
|
Valved cardiac conduit |
This attribute represents the site where the device is intended to reside in or on the body. |
True |
Heart structure |
Inferred relationship |
Some |
|
Conduit with homograft valve |
This attribute represents the site where the device is intended to reside in or on the body. |
True |
Heart structure |
Inferred relationship |
Some |
|
Conduit with xenograft valve |
This attribute represents the site where the device is intended to reside in or on the body. |
True |
Heart structure |
Inferred relationship |
Some |
|
Conduit with mechanical prosthetic valve |
This attribute represents the site where the device is intended to reside in or on the body. |
True |
Heart structure |
Inferred relationship |
Some |
|
Cardiac conduit |
This attribute represents the site where the device is intended to reside in or on the body. |
True |
Heart structure |
Inferred relationship |
Some |
|
Interatrial baffle |
This attribute represents the site where the device is intended to reside in or on the body. |
True |
Heart structure |
Inferred relationship |
Some |
|
Cardiac assist implant |
This attribute represents the site where the device is intended to reside in or on the body. |
True |
Heart structure |
Inferred relationship |
Some |
|
Prosthetic heart |
This attribute represents the site where the device is intended to reside in or on the body. |
True |
Heart structure |
Inferred relationship |
Some |
|
Artificial heart, permanent |
This attribute represents the site where the device is intended to reside in or on the body. |
True |
Heart structure |
Inferred relationship |
Some |
|
Single-chamber implantable defibrillator (physical object) |
This attribute represents the site where the device is intended to reside in or on the body. |
True |
Heart structure |
Inferred relationship |
Some |
|
Cardiac myoplasty electrical stimulation system lead |
This attribute represents the site where the device is intended to reside in or on the body. |
True |
Heart structure |
Inferred relationship |
Some |
|
Cardiac contractility modulation system pulse generator (physical object) |
This attribute represents the site where the device is intended to reside in or on the body. |
True |
Heart structure |
Inferred relationship |
Some |
|
Cardiac occluder (physical object) |
This attribute represents the site where the device is intended to reside in or on the body. |
True |
Heart structure |
Inferred relationship |
Some |
|
Dual-chamber implantable defibrillator (physical object) |
This attribute represents the site where the device is intended to reside in or on the body. |
True |
Heart structure |
Inferred relationship |
Some |
|
Cardiac resynchronization therapy implantable defibrillator |
This attribute represents the site where the device is intended to reside in or on the body. |
True |
Heart structure |
Inferred relationship |
Some |
|
Subcutaneous implantable cardioverter defibrillator (physical object) |
This attribute represents the site where the device is intended to reside in or on the body. |
True |
Heart structure |
Inferred relationship |
Some |
|
Replacement of temporary transvenous electrode of dual chamber pulse generator (procedure) |
Procedure site - Indirect (attribute) |
True |
Heart structure |
Inferred relationship |
Some |
1 |
Removal of cardiac pacemaker and replacement with single-chamber cardiac device (procedure) |
Procedure site - Indirect (attribute) |
True |
Heart structure |
Inferred relationship |
Some |
2 |
Replacement of cardiac pacemaker with single chamber pacemaker not specified as rate responsive |
Procedure site - Indirect (attribute) |
True |
Heart structure |
Inferred relationship |
Some |
2 |
Removal of cardiac pacemaker with replacement by single-chamber device, rate-responsive (procedure) |
Procedure site - Indirect (attribute) |
True |
Heart structure |
Inferred relationship |
Some |
2 |
Replacement of cardioverter defibrillator (procedure) |
Procedure site - Indirect (attribute) |
True |
Heart structure |
Inferred relationship |
Some |
1 |
Replacement of pulse generator of implantable cardioverter defibrillator using fluoroscopic guidance (procedure) |
Procedure site - Indirect (attribute) |
True |
Heart structure |
Inferred relationship |
Some |
2 |
Removal of electronic heart device |
Procedure site - Indirect (attribute) |
True |
Heart structure |
Inferred relationship |
Some |
1 |
Removal of automatic implantable cardioverter/defibrillator pads and electrodes |
Procedure site - Indirect (attribute) |
True |
Heart structure |
Inferred relationship |
Some |
1 |
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by vertebral segmentation defects associated with cardiac (patent ductus arteriosus, atrial septal defect, hypoplastic left heart) and renal (hypoplastic kidneys, chronic kidney disease) anomalies. Additional reported features include limb defects, short stature, global developmental delay, intellectual disability, and sensorineural hearing loss, among others. |
Finding site |
True |
Heart structure |
Inferred relationship |
Some |
3 |
Pacemaker programmer |
This attribute represents the site where the device is intended to reside in or on the body. |
True |
Heart structure |
Inferred relationship |
Some |
|
Cardiac contractility modulation system |
This attribute represents the site where the device is intended to reside in or on the body. |
True |
Heart structure |
Inferred relationship |
Some |
|
Cardiac contractility modulation system programmer |
This attribute represents the site where the device is intended to reside in or on the body. |
True |
Heart structure |
Inferred relationship |
Some |
|
Defibrillator programmer |
This attribute represents the site where the device is intended to reside in or on the body. |
True |
Heart structure |
Inferred relationship |
Some |
|
Cardiac myoplasty electrical stimulation system programmer |
This attribute represents the site where the device is intended to reside in or on the body. |
True |
Heart structure |
Inferred relationship |
Some |
|
Cardiac contractility modulation system charger |
This attribute represents the site where the device is intended to reside in or on the body. |
True |
Heart structure |
Inferred relationship |
Some |
|
Cardiac myoplasty electrical stimulation system (physical object) |
This attribute represents the site where the device is intended to reside in or on the body. |
True |
Heart structure |
Inferred relationship |
Some |
|
Removal of cardiac pacemaker using fluoroscopic guidance with contrast (procedure) |
Procedure site - Indirect (attribute) |
True |
Heart structure |
Inferred relationship |
Some |
1 |
Removal of electrocardiography loop recorder (procedure) |
Procedure site - Indirect (attribute) |
True |
Heart structure |
Inferred relationship |
Some |
2 |
Removal of cardiac monitoring implant using fluoroscopic guidance (procedure) |
Procedure site - Indirect (attribute) |
True |
Heart structure |
Inferred relationship |
Some |
3 |
Cardiac resynchronization therapy defibrillator pulse generator |
This attribute represents the site where the device is intended to reside in or on the body. |
True |
Heart structure |
Inferred relationship |
Some |
|
Neonatal cardiac arrest |
Finding site |
True |
Heart structure |
Inferred relationship |
Some |
1 |
Fetal cardiac arrest |
Finding site |
True |
Heart structure |
Inferred relationship |
Some |
1 |
Fluoroscopic angiography with contrast and aspiration of heart (procedure) |
Procedure site |
True |
Heart structure |
Inferred relationship |
Some |
2 |
Doppler ultrasonography of fetal heart for heart sounds (procedure) |
Procedure site - Direct (attribute) |
True |
Heart structure |
Inferred relationship |
Some |
1 |
Fetal echocardiography (procedure) |
Procedure site - Direct (attribute) |
True |
Heart structure |
Inferred relationship |
Some |
1 |
Magnetic resonance imaging of fetal heart (procedure) |
Procedure site - Direct (attribute) |
True |
Heart structure |
Inferred relationship |
Some |
1 |
Division of common wall between posterior left atrium and coronary sinus with roofing of resultant defect and patch graft (procedure) |
Procedure site - Direct (attribute) |
True |
Heart structure |
Inferred relationship |
Some |
3 |
Preinfarction syndrome due to arteriosclerosis of nonautologous biological coronary artery bypass graft (disorder) |
Finding site |
True |
Heart structure |
Inferred relationship |
Some |
1 |
Cardiac arrest during cardiac surgery (disorder) |
Finding site |
False |
Heart structure |
Inferred relationship |
Some |
1 |
Andersen Tawil syndrome (disorder) |
Finding site |
False |
Heart structure |
Inferred relationship |
Some |
3 |
Aortic valve disorder in mother complicating childbirth |
Finding site |
True |
Heart structure |
Inferred relationship |
Some |
2 |
Mitral valve disorder in mother complicating childbirth (disorder) |
Finding site |
True |
Heart structure |
Inferred relationship |
Some |
2 |
Postpartum cardiomyopathy |
Finding site |
True |
Heart structure |
Inferred relationship |
Some |
4 |