80891009: Heart structure (body structure)

SNOMED CT Concept\Body structure (body structure)\Anatomical or acquired body structure (body structure)\Anatomical structure\...

\Anatomical structure which has as its parts a heterogeneous collection of organs, organ parts, cells, cell parts or body part subdivisions that are adjacent to, or continuous with one another; does not constitute a cell part, cell, tissue, organ, or body part subdivision.\Structure of anatomical compartment (body structure)\Structure of body cavity and/or content\Structure of thoracic cavity and/or content\...

\Intrathoracic cardiovascular structure\Heart and/or pericardium structure\Heart structure

\Mediastinal structure\Region of mediastinum\Structure of inferior mediastinum (body structure)\Subdivision of inferior mediastinum\Middle mediastinum structure\Heart and/or pericardium structure\Heart structure

\Structure of thoracic viscus\Heart structure

\An anatomical structure that consists of the maximal set of organ parts so connected to one another that together they constitute a self-contained unit of macroscopic anatomy, distinct both morphologically and functionally from other such units. Together with other organs, an organ constitutes an organ system or a body part. An organ is divisible into organ parts but not organs (examples: femur, biceps, liver, heart, aorta, sciatic nerve, ovary).\Structure of viscus\Structure of thoracic viscus\Heart structure

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Heart structure	Is a	Cardiac structure	false	Inferred relationship	Some
Heart structure	Is a	Intrathoracic cardiovascular structure	false	Inferred relationship	Some
Heart structure	Is a	Structure of thoracic viscus	true	Inferred relationship	Some
Heart structure	partie de	Entire heart AND pericardium	false	Additional relationship	Some
Heart structure	Is a	Heart and/or pericardium structure	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Common arterial trunk with pulmonary arteries arising from trunk and unobstructed aortic arch (disorder)	Finding site	True	Heart structure	Inferred relationship	Some	2
Common arterial trunk with crossed over pulmonary arteries (disorder)	Finding site	True	Heart structure	Inferred relationship	Some	2
Common arterial trunk with pulmonary origin from truncal valve sinus (disorder)	Finding site	True	Heart structure	Inferred relationship	Some	2
Common arterial trunk with isolated pulmonary artery (disorder)	Finding site	True	Heart structure	Inferred relationship	Some	2
Toxoplasma myocarditis	Finding site	False	Heart structure	Inferred relationship	Some	3
Myocarditis caused by Aspergillus (disorder)	Finding site	False	Heart structure	Inferred relationship	Some	1
infection de greffe cardiaque	Finding site	False	Heart structure	Inferred relationship	Some	1
Myocarditis due to infectious agent	Finding site	False	Heart structure	Inferred relationship	Some	2
Myocarditis caused by Candida	Finding site	False	Heart structure	Inferred relationship	Some	1
Enterovirus heart infection	Finding site	True	Heart structure	Inferred relationship	Some	1
Coxsackie carditis	Finding site	False	Heart structure	Inferred relationship	Some	2
Chagas' disease with heart involvement	Finding site	False	Heart structure	Inferred relationship	Some	1
Coxsackie myocarditis	Finding site	False	Heart structure	Inferred relationship	Some	2
Fungal myocarditis	Finding site	False	Heart structure	Inferred relationship	Some	2
Coxsackie myocarditis of newborn (disorder)	Finding site	False	Heart structure	Inferred relationship	Some	2
Infectious disease of heart	Finding site	True	Heart structure	Inferred relationship	Some	1
Acute myocarditis - toxoplasmosis	Finding site	False	Heart structure	Inferred relationship	Some	2
Parasitic myocarditis	Finding site	False	Heart structure	Inferred relationship	Some	2
Acute myocarditis - coxsackie	Finding site	False	Heart structure	Inferred relationship	Some	2
Acute Chagas' disease with heart involvement	Finding site	False	Heart structure	Inferred relationship	Some	2
Acute Chagas' disease with heart involvement	Finding site	True	Heart structure	Inferred relationship	Some	5
Cardiac disorder due to typhoid fever (disorder)	Finding site	True	Heart structure	Inferred relationship	Some	2
Tuberculosis of heart	Finding site	True	Heart structure	Inferred relationship	Some	2
Viral carditis	Finding site	False	Heart structure	Inferred relationship	Some	2
Resting ischaemia	Finding site	True	Heart structure	Inferred relationship	Some	3
Fluoroscopy guided removal of automatic cardiac defibrillator	Procedure site - Direct (attribute)	True	Heart structure	Inferred relationship	Some	2
Fluoroscopy guided removal of automatic cardiac defibrillator	Procedure site - Indirect (attribute)	False	Heart structure	Inferred relationship	Some	3
Heart disease co-occurrent with human immunodeficiency virus infection (disorder)	Finding site	True	Heart structure	Inferred relationship	Some	1
Subacute ischaemic heart disease	Finding site	True	Heart structure	Inferred relationship	Some	2
Intraoperative cardiorespiratory arrest (disorder)	Finding site	False	Heart structure	Inferred relationship	Some	2
Removal of cardiac pacemaker using fluoroscopic guidance with contrast (procedure)	Procedure site - Direct (attribute)	True	Heart structure	Inferred relationship	Some	2
Removal of cardiac pacemaker using fluoroscopic guidance with contrast (procedure)	Procedure site - Indirect (attribute)	False	Heart structure	Inferred relationship	Some	3
A rare disorder that manifest in adults and generally present with a variety of non-specific manifestations (depending on tumor site and infiltration) such as weight loss, exhaustion, hemorrhagic pericardial effusion, heart failure, arrhythmias, and embolisms, or that can also be asymptomatic. In adults 75% of heart tumors are benign, with myxoma being the most common benign tumor (accounting for 50-70% of all primary heart tumors) and rhabdomyosarcoma comprising 75% of malignant heart tumors. Other malignant tumors of the heart include fibrosarcoma and leiomyosarcoma.	Finding site	True	Heart structure	Inferred relationship	Some	1
Cardiac arrest during surgery (disorder)	Finding site	False	Heart structure	Inferred relationship	Some	2
Long QT syndrome caused by drug (disorder)	Finding site	False	Heart structure	Inferred relationship	Some	3
72 hour ambulatory electrocardiographic monitoring (procedure)	Procedure site - Direct (attribute)	True	Heart structure	Inferred relationship	Some	1
Cardiac tumors are benign or malignant neoplasms arising primarily in the inner lining, muscle layer, or the surrounding pericardium of the heart. They can be primary or metastatic.	Finding site	True	Heart structure	Inferred relationship	Some	1
Thomas syndrome is characterized by renal anomalies, cardiac malformations and cleft lip or palate. It has been described in six patients. Transmission was suggested to be autosomal recessive.	Finding site	False	Heart structure	Inferred relationship	Some	3
A rare congenital cardiac malformation that is a variant of an atrioventricular septal defect (AVSD) with an interatrial communication (ostium primum defect) just above the common atrioventricular (AV) valve, no interventricular communication just below the atrioventricular valve, a common atrioventricular junction but separate right and left atrioventricular valvar orifices, and a three-leaflet, left-sided component of the common atrioventricular valve (cleft). Shunting is restricted to the atrial level because of fusion of the leaflets of the common AV valve with the crest of the ventricular septum.	Finding site	True	Heart structure	Inferred relationship	Some	2
A very rare syndrome described in three siblings of one Japanese family and characterized by congenital heart disease, round face with depressed nasal bridge, small mouth, short stature, and relatively dark skin and typical dermatoglyphic anomalies, and intellectual deficit.	Finding site	False	Heart structure	Inferred relationship	Some	3
Orofaciodigital syndrome type 11 is an extremely rare, sporadic form of Orofaciodigital syndrome with only a few reported cases, and characterized by facial (blepharophimosis, bulbous nasal tip, broad nasal bridge, downslanting palpebral fissures and low set ears) and skeletal (post-axial polydactyly and fusion of vertebrae) malformations along with severe intellectual disability, deafness and congenital heart defects.	Finding site	False	Heart structure	Inferred relationship	Some	12
Cranio-cerebello-cardiac (3C) syndrome is a rare multiple congenital anomalies syndrome characterised by craniofacial (prominent occiput and forehead, hypertelorism, ocular coloboma, cleft palate), cerebellar (Dandy-Walker malformation, cerebellar vermis hypoplasia) and cardiac (tetralogy of Fallot, atrial and ventricular septal defects) anomalies.	Finding site	False	Heart structure	Inferred relationship	Some	6
Microcephaly-facio-cardio-skeletal syndrome, Hadziselimovic type is a rare syndrome with cardiac malformations, characterized by prenatal-onset growth retardation (low birth weight and short stature), hypotonia, developmental delay and intellectual disability associated with microcephaly and craniofacial (low anterior hairline, hypotelorism, thick lips with carp-shaped mouth, high-arched palate, low-set ears), cardiac and skeletal (hypoplastic thumbs and first metacarpals) abnormalities.	Finding site	False	Heart structure	Inferred relationship	Some	4
A rare multiple congenital anomaly syndrome characterized by flat face, hypertelorism, flat occiput, upward slanting palpebral fissures, cleft palate, micrognathia, short neck, and severe congenital heart defects. Malrotation of the intestine, bilateral clinodactyly, bilobed tongue, short fourth metatarsals and bifid thumbs may be additionally observed.	Finding site	False	Heart structure	Inferred relationship	Some	5
Focused transthoracic echocardiography in intensive care (procedure)	Procedure site - Direct (attribute)	True	Heart structure	Inferred relationship	Some	1
A rare multiple congenital anomaly syndrome characterized by flat face, hypertelorism, flat occiput, upward slanting palpebral fissures, cleft palate, micrognathia, short neck, and severe congenital heart defects. Malrotation of the intestine, bilateral clinodactyly, bilobed tongue, short fourth metatarsals and bifid thumbs may be additionally observed.	Finding site	True	Heart structure	Inferred relationship	Some	4
Microcephaly - cardiac defect - lung malsegmentation syndrome is a very rare syndrome characterized by the combination of microcephaly, heart defects, renal hypoplasia, lung segmentation defects and cleft palate.	Finding site	False	Heart structure	Inferred relationship	Some	3
Intravenous cardiac arrhythmia drug challenge test using fluoroscopic guidance with contrast (procedure)	Procedure site - Direct (attribute)	True	Heart structure	Inferred relationship	Some	2
Timothy syndrome is a multi-system disorder with characteristics of cardiac, hand, facial and neurodevelopmental features that include QT prolongation, webbed fingers and toes, flattened nasal bridge, low-set ears, small upper jaw, thin upper lip, and characteristic features of autism or autistic spectrum disorders. Timothy syndrome is caused by mutations in the CACNA1C gene. It is inherited as autosomal dominant trait. Researchers have identified two forms of Timothy syndrome. Type 1, which is also known as the classic type, includes all of the characteristic features described above. Type 2, or the atypical type, causes a more severe form of long QT syndrome and a greater risk of arrhythmia and sudden death. Unlike the classic type, the atypical type does not appear to cause webbing of the fingers or toes.	Finding site	True	Heart structure	Inferred relationship	Some	2
Cardiac anomalies-heterotaxy syndrome is characterized by non-compaction of the ventricular myocardium, bradycardia, pulmonary valve stenosis, and secundum atrial septal defect. Laterality sequence anomalies are also present. So far, the syndrome has been described in nine members from three generations of the same family. Transmission is autosomal dominant and linkage to chromosome 6p24.3-21.2 was reported.	Finding site	True	Heart structure	Inferred relationship	Some	1
A rare, multiple congenital anomalies syndrome with intellectual disability commonly characterized by facial dysmorphism (e.g. sagittal craniosynostosis, hypertelorism, strabismus, low-set dysplastic ears, retrognathia or micrognathia, mandibular ankyloses, cleft palate, aplasia uvulae), congenital heart defects (e.g. atrioventricular septal defect, anomalous venous return), genital anomalies (e.g. cryptorchidism, microphallus), as well as growth delay and intellectual disability. In some cases, tracheobronchial anomalies, large joint contractures, syndactyly, rib anomalies and hypoplastic kidneys are reported. Rarely, no cardiac anomaly may be reported.	Finding site	False	Heart structure	Inferred relationship	Some	3
Bosley-Salih-Alorainy syndrome (BSAS) is characterised by variable horizontal gaze dysfunction, profound and bilateral sensorineural deafness associated commonly with severe inner ear maldevelopment, cerebrovascular anomalies (ranging from unilateral internal carotid artery hypoplasia to bilateral agenesis), cardiac malformation, developmental delay and occasionally autism. The syndrome is caused by homozygous mutations in the HOXA1 gene (7p15.2) and is transmitted in an autosomal recessive manner. The syndrome overlaps clinically and genetically with Athabaskan brain dysfunction syndrome (ABDS,). However unlike ABDS, BSAS does not manifest central hypoventilation.	Finding site	False	Heart structure	Inferred relationship	Some	2
A rare, multiple congenital anomalies syndrome with intellectual disability commonly characterized by facial dysmorphism (e.g. sagittal craniosynostosis, hypertelorism, strabismus, low-set dysplastic ears, retrognathia or micrognathia, mandibular ankyloses, cleft palate, aplasia uvulae), congenital heart defects (e.g. atrioventricular septal defect, anomalous venous return), genital anomalies (e.g. cryptorchidism, microphallus), as well as growth delay and intellectual disability. In some cases, tracheobronchial anomalies, large joint contractures, syndactyly, rib anomalies and hypoplastic kidneys are reported. Rarely, no cardiac anomaly may be reported.	Finding site	True	Heart structure	Inferred relationship	Some	2
CHIME syndrome is a rare ectodermal dysplasia syndrome characterized by ocular colobomas, cardiac defects, ichthyosiform dermatosis, intellectual disability, conductive hearing loss and epilepsy.	Finding site	False	Heart structure	Inferred relationship	Some	7
A rare multiple congenital anomalies/dysmorphic syndrome characterized by skeletal dysplasia (including coronal clefting of the vertebral bodies and short limbs and variable congenital heart malformations, such as atrial and ventricular septal defects, right ventricular hypoplasia, and valve defects). There have been no further descriptions in the literature since 1990.	Finding site	False	Heart structure	Inferred relationship	Some	3
Heart-hand syndrome type 3 is a very rare heart-hand syndrome, described in three members of a Spanish family to date, which is characterized by a cardiac conduction defect (sick sinus, bundle-branch block) and brachydactyly, resembling brachydactyly type C of the hands, affecting principally the middle phalanges in conjunction with an extra ossicle on the proximal phalanx of both index fingers. Feet abnormalities are more subtle.	Finding site	False	Heart structure	Inferred relationship	Some	6
Short stature-webbed neck-heart disease syndrome is characterized by short stature, intellectual deficit, facial dysmorphism, short, webbed neck, skin changes and congenital heart defects. It has been reported in four Arab Bedouin siblings born to consanguineous parents.	Finding site	False	Heart structure	Inferred relationship	Some	3
Angina co-occurrent and due to coronary arteriosclerosis (disorder)	Finding site	True	Heart structure	Inferred relationship	Some	4
Chagas' disease with heart involvement	Finding site	True	Heart structure	Inferred relationship	Some	5
Angina co-occurrent and due to arteriosclerosis of coronary artery bypass graft (disorder)	Finding site	True	Heart structure	Inferred relationship	Some	5
Heart-hand syndrome type 2 is an extremely rare heart-hand syndrome described in two families to date, that is characterized by upper limb malformations (brachytelephalangy type D, hypoplastic deltoids, mild shortening of the fourth and fifth metacarpals in some individuals, skeletal anomalies in the humerus, radius, ulnae, and thenar bones) and cardiac arrhythmias (junctional rhythms and atrial fibrillation).	Finding site	True	Heart structure	Inferred relationship	Some	2
Systolic heart failure stage B due to ischemic cardiomyopathy (disorder)	Finding site	True	Heart structure	Inferred relationship	Some	4
Systolic heart failure stage C due to ischaemic cardiomyopathy	Finding site	True	Heart structure	Inferred relationship	Some	4
Unstable angina co-occurrent and due to coronary arteriosclerosis (disorder)	Finding site	True	Heart structure	Inferred relationship	Some	4
Beemer-Ertbruggen syndrome is a lethal malformation syndrome reported in 2 brothers of first-cousin parents that is characterized by hydrocephalus, cardiac malformation, dense bones, and unusual facies with down-slanting palpebral fissures, bulbous nose, broad nasal bridge, micrognathia and a long upper lip. There have been no further descriptions in the literature since 1984.	Finding site	False	Heart structure	Inferred relationship	Some	5
A rare multiple congenital anomalies/dysmorphic syndrome characterized by intrauterine growth retardation, multiple congenital malformations (such as brain malformations including ectopic neuro-pituitary gland, hypoplastic adenopituitary, and hypoplastic cerebellar vermis, cardiac and renal anomalies, and postaxial polydactyly), abnormal hair structure with temporal balding, and dysmorphic facial features with hypoplastic nasal bridge, anteverted nostrils, dysplastic ears, long and smooth philtrum, narrow upper lip, and prominent, asymmetric lower lip. Postnatal growth retardation and severe developmental delay have also been reported.	Finding site	False	Heart structure	Inferred relationship	Some	7
Primary angiosarcoma of heart (disorder)	Finding site	True	Heart structure	Inferred relationship	Some	1
A rare genetic disease characterized by the association of unilateral complete or partial lung agenesis, complex congenital cardiac anomalies such as atrial septal defect, total anomalous pulmonary venous return, or patent ductus arteriosus, and ipsilateral or bilateral thumb abnormalities. Presence of facial dysmorphism and other malformative features has also been reported.	Finding site	False	Heart structure	Inferred relationship	Some	4
Acute kidney injury caused by heart failure. Also known as Cardiorenal syndrome type 1.	Finding site	False	Heart structure	Inferred relationship	Some	1
Kallmann syndrome with cardiopathy is characterized by hypogonadotropic hypogonadism associated with gonadotropin-releasing hormone (GnRH) deficiency, anosmia or hyposmia (with hypoplasia or aplasia of the olfactory bulbs) and complex congenital cardiac malformations (double-outlet right ventricle, dilated cardiomyopathy, right aortic arch). It represents a distinct clinical entity from Kallmann syndrome.	Finding site	False	Heart structure	Inferred relationship	Some	5
Cardiac complication of anesthesia during the puerperium (disorder)	Finding site	True	Heart structure	Inferred relationship	Some	2
Obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome is characterized by precocious obesity, congenital hypothyroidism, neonatal colitis, cardiac hypertrophy, craniosynostosis and developmental delay. It has been described in two brothers, one of whom died within the first month of life. The parents of the two children were nonconsanguineous and in good health, however, the pregnancies were complicated by a maternal HELLP syndrome (Haemolysis, Elevated Liver enzymes and Low Platelets). The mode of inheritance has not yet been clearly established.	Finding site	False	Heart structure	Inferred relationship	Some	9
Meacham syndrome is a multiple malformation syndrome characterized by congenital diaphragmatic abnormalities, genital defects and cardiac malformations.	Finding site	False	Heart structure	Inferred relationship	Some	5
A rare, syndromic diabetes mellitus characterized by partial pancreatic agenesis, diabetes mellitus, and heart anomalies (including transposition of the great vessels, ventricular or atrial septal defects, pulmonary stenosis, or patent ductus arteriosis).	Finding site	False	Heart structure	Inferred relationship	Some	3
Neonatal cardiac failure due to decreased left ventricular output (disorder)	Finding site	True	Heart structure	Inferred relationship	Some	1
Chronic Chagas disease with heart involvement	Finding site	True	Heart structure	Inferred relationship	Some	3
Rupture of heart	Finding site	True	Heart structure	Inferred relationship	Some	2
Cardiac rupture due to and following acute myocardial infarction (disorder)	Finding site	True	Heart structure	Inferred relationship	Some	2
Biologic cardiac valve prosthesis in situ	Finding site	False	Heart structure	Inferred relationship	Some	1
Metal mitral valve prosthesis in situ	Finding site	False	Heart structure	Inferred relationship	Some	1
Intracardiac pressure	This attribute specifies the independent continuant which bears the quality, and on which the dependent quality (of this observable) depends.	False	Heart structure	Inferred relationship	Some	3
A very rare syndrome characterized by intellectual deficit, horseshoe kidney, and congenital heart defects.	Finding site	False	Heart structure	Inferred relationship	Some	4
A very rare syndrome characterized by intellectual deficit, horseshoe kidney, and congenital heart defects.	Finding site	True	Heart structure	Inferred relationship	Some	3
A rare, multiple congenital anomalies/dysmorphic syndrome characterized by microcephaly, intellectual disability, seizures, and congenital heart defects (e.g. atrial/ventricular septal defect, hypoplastic aortic arch with persistent ductus arteriosus). Additional manifestations include mild hypothyroidism, skeletal abnormalities, micropenis, delayed psychomotor development, dysmorphic facial features (including epicanthus, depressed nasal bridge, prominent antitragus), and pulmonary vascular occlusive disease. There have been no further descriptions in the literature since 1989.	Finding site	False	Heart structure	Inferred relationship	Some	3
Positron emission tomography with computed tomography of heart (procedure)	Procedure site - Direct (attribute)	True	Heart structure	Inferred relationship	Some	2
Positron emission tomography with computed tomography of heart (procedure)	Procedure site - Direct (attribute)	True	Heart structure	Inferred relationship	Some	3
A rare, life-threatening developmental defect during embryogenesis characterized by polysyndactyly of fingers and toes as well as complex congenital heart defects (e.g. atrioventricular septal defects, aortic dextroposition, single ventricle, hypo- or hypertrophy of one side of the heart). Additional features may include dysmorphic traits (large fontanel, high forehead, ptosis, hypertelorism, epicanthus, low-set malformed ears, prominent root of the nose, bulbous nose, anteverted nares, long and smooth philtrum, thin upper lip, micrognathism, hirsutism, single transverse crease) nail hypoplasia, phalange agenesis/hypoplasia, flexion contractures, polysplenia, multiple hepatic/renal cysts, atrophic biliary vesicle, ductal plate malformation and genital anomalies (e.g. micropenis, undescended testes, hypoplastic scrotum). The syndrome is usually fatal in utero or in infancy, but survival cases have been reported.	Finding site	False	Heart structure	Inferred relationship	Some	2
Myocardial ischemia during surgery (disorder)	Finding site	False	Heart structure	Inferred relationship	Some	2
A rare syndromic central nervous system malformation characterized by the association of conotruncal heart defects, myelomeningocele and craniofacial dysmorphism similar to that seen in monosomy 22q11.	Finding site	False	Heart structure	Inferred relationship	Some	6
Arrhythmia during surgery (disorder)	Finding site	False	Heart structure	Inferred relationship	Some	1
Neonatal cardiac failure due to pulmonary overperfusion (disorder)	Finding site	True	Heart structure	Inferred relationship	Some	2
Cataract-congenital heart disease-neural tube defect syndrome is a multiple congenital anomaly syndrome characterized by sacral neural tube defects resulting in tethered cord, atrial and/or ventricular septal heart defects (that are detected in infancy), bilateral, symmetrical hyperopia, rapidly progressive early childhood cataracts, bilateral aphakic glaucoma, and abnormal facial features (low frontal hairline, small ears, short philtrum, prominent, widely spaced central incisors, and micrognathia). Hypotonia, growth and developmental delay, seizures, and joint limitation are also reported.	Finding site	False	Heart structure	Inferred relationship	Some	9
A rare endocrine disease characterized by lentigines with a specific peri-orifical distribution, blue nevus, myxomas, various endocrine tumors including primary pigmented nodular adrenocortical disease (PPNAD), acromegaly, thyroid tumors, and a wide range of other tumors.	Finding site	False	Heart structure	Inferred relationship	Some	3
A rare autosomal dominant heart-hand syndrome that is characterized by bisymmetric brachydactyly accompanied by long thumbs, joint anomalies (restriction of motion at the shoulder and metacarpophalangeal joints) and cardiac conduction defects. Additional features include small hands and feet, clinodactyly, narrow shoulders with short clavicles, pectus excavatum and mild shortness of the limbs, cardiomegaly and murmur of pulmonic stenosis. There have been no new reports since 1981.	Finding site	False	Heart structure	Inferred relationship	Some	6
Abnormal cardiotochogram tracing (finding)	Finding site	True	Heart structure	Inferred relationship	Some	2
Normal CTG tracing	Finding site	True	Heart structure	Inferred relationship	Some	2
Cardiac arrest due to administration of anesthesia in pregnancy	Finding site	True	Heart structure	Inferred relationship	Some	1
Contusion of heart without hemopericardium	Finding site	False	Heart structure	Inferred relationship	Some	1
Laceration of heart without hemopericardium (disorder)	Finding site	True	Heart structure	Inferred relationship	Some	1
Contusion of heart co-occurrent with hemopericardium (disorder)	Finding site	True	Heart structure	Inferred relationship	Some	2
Revision of internal cardiac defibrillator lead using fluoroscopic guidance (procedure)	Procedure site - Direct (attribute)	False	Heart structure	Inferred relationship	Some	4

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Reference Sets

Anatomy structure and entire association reference set (foundation metadata concept)

Anatomy structure and part association reference set (foundation metadata concept)

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Id	Description	Lang	Type	Status	Case?	Module
134173012	Heart	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
504537016	Heart structure	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
822101011	Heart structure (body structure)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2478860016	Cardiac structure	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
12301000077119	structure du cœur	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
117621000087110	cœur	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
919721000172117	structure cardiaque	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
965851000172118	cor	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module