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783804002: Abnormal communication (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3760424014 Abnormal communication en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3760425010 Abnormal communication (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3760426011 Anomalous connection en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

39 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Abnormal communication Is a Morphologically abnormal structure true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Recurrent ventricular component of atrioventricular septal defect after prior cardiovascular surgical procedure (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Acquired excessive restriction of interatrial communication Associated morphology True Abnormal communication Inferred relationship Some 1
Excessive restriction of interatrial communication as complication of procedure Associated morphology True Abnormal communication Inferred relationship Some 1
Atrioventricular septal defect with additional muscular ventricular septal defect (disorder) Associated morphology True Abnormal communication Inferred relationship Some 2
Acquired atrial septal defect (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Acquired ventricular septal defect (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Ventricular septal defect following procedure (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Laubry-Pezzi syndrome is a rare, non-syndromic, congenital heart malformation characterized by the prolapse of an aortic valve cusp into a subjacent ventricular septal defect due to Venturi effect, resulting in aortic regurgitation. Patients typically present with symptoms of progressive aortic valve insufficiency, such as shortness of breath, heart palpitations, chest pain and exercise intolerance. Associated morphology True Abnormal communication Inferred relationship Some 1
Pulmonary valve agenesis-tetralogy of Fallot-absence of ductus arteriosus syndrome is a rare congenital heart malformation characterized by a tetralogy of Fallot (pulmonary stenosis, overriding aorta, ventricular septal defect and right ventricular hypertrophy), complete absence or rudimentary pulmonary valve that is both stenotic and regurgitant and an absence of the ductus arteriosus. It presents prenatally with cardiomegaly, polyhydramnios, fetal heart failure, hydrops fetalis and fetal demise or postnatally with cyanosis and respiratory failure due to bronchomalacia secondary to bronchial compression from dilated pulmonary arteries. It is frequently associated with 22q11 deletion. Associated morphology True Abnormal communication Inferred relationship Some 4
Congenital ventricular septal defect Associated morphology True Abnormal communication Inferred relationship Some 1
Eisenmenger ventricular septal defect (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Pentalogy of Fallot Associated morphology True Abnormal communication Inferred relationship Some 1
Pentalogy of Fallot Associated morphology True Abnormal communication Inferred relationship Some 4
Ventricular septal defect with malaligned outlet septum (disorder) Associated morphology True Abnormal communication Inferred relationship Some 2
Muscular ventricular septal defect in trabecular septum (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Tetralogy of Fallot Associated morphology True Abnormal communication Inferred relationship Some 4
A rare multiple congenital anomalies/dysmorphic syndrome characterized by auditory canal atresia (resulting in moderate conductive hearing loss) associated with intellectual disability, ventricular septal defect, umbilical hernia, anteriorly displaced anus, various skeletal anomalies (such as mild clubfoot, long fifth fingers, proximally placed thumbs), and craniofacial dysmorphism which includes brachycephaly, prominent forehead, flattened occiput, midface hypoplasia, anteverted nares, and low set, posteriorly rotated ears with overlapping superior helix. There have been no further descriptions in the literature since 1987. Associated morphology True Abnormal communication Inferred relationship Some 2
Fallot complex - intellectual deficit - growth delay is a rare disorder characterized by tetralogy of Fallot, minor facial anomalies, and severe intellectual deficiency and growth delay. Associated morphology True Abnormal communication Inferred relationship Some 3
An extremely rare genetic congenital heart disease characterized by the presence of atrial septal defect, mostly of the ostium secundum type, associated with conduction anomalies like atrioventricular block, atrial fibrillation or right bundle branch block. Associated morphology True Abnormal communication Inferred relationship Some 1
Tetralogy of Fallot with atresia of pulmonary valve (disorder) Associated morphology True Abnormal communication Inferred relationship Some 2
Double outlet right ventricle with subaortic or doubly committed ventricular septal defect without pulmonary stenosis - ventricular septal defect type (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Acquired cardiac septal defect (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Perimembranous ventricular septal defect Associated morphology True Abnormal communication Inferred relationship Some 1
Tetralogy of Fallot with pulmonary atresia and systemic-to-pulmonary collateral artery Associated morphology True Abnormal communication Inferred relationship Some 4
Haemodynamically insignificant ventricular septal defect Associated morphology True Abnormal communication Inferred relationship Some 1
Eisenmenger's syndrome (disorder) Associated morphology True Abnormal communication Inferred relationship Some 2
Ventricular septal defect with absent outlet septum and overriding truncal valve (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Pulmonary atresia with ventricular septal defect Associated morphology True Abnormal communication Inferred relationship Some 2
Interatrial communication through coronary sinus orifice (disorder) Associated morphology True Abnormal communication Inferred relationship Some 2
Ventricular septal defect with anterior malaligned outlet septum with overriding pulmonary valve (disorder) Associated morphology True Abnormal communication Inferred relationship Some 2
Ventricular septal defect with posterior malaligned outlet septum with overriding aortic valve (disorder) Associated morphology True Abnormal communication Inferred relationship Some 2
Ventricular septal defect with posterior malaligned outlet septum with overriding pulmonary valve (disorder) Associated morphology True Abnormal communication Inferred relationship Some 3
Ventricular septal defect with anterior malaligned outlet septum with overriding aortic valve (disorder) Associated morphology True Abnormal communication Inferred relationship Some 2
Restrictive interatrial communication with obligatory shunt (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Pulmonary atresia and ventricular septal defect with aorta from left ventricle (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Pulmonary atresia and ventricular septal defect with aorta from right ventricle (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Ventricular septal defect of inlet of right aspect of ventricular septum (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Nonfenestrated interatrial communication within oval fossa (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Residual ventricular septal defect (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Pulmonary atresia with ventricular septal defect of Fallot type (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Nonrestrictive interatrial communication (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Restrictive interatrial communication (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Absent pulmonary valve syndrome with ventricular septal defect of non Fallot type (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Double outlet right ventricle with doubly committed ventricular septal defect and pulmonary stenosis (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Fenestrated interatrial communication within oval fossa (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Ventricular septal defect with absent outlet septum and overriding truncal valve with extension of membranous septum (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Double outlet right ventricle with subpulmonary ventricular septal defect (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Ventricular septal defect with absent outlet septum and overriding truncal valve with inferior muscular rim (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Subarterial ventricular septal defect (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Doubly committed ventricular septal defect in double outlet ventriculoarterial connection (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Residual interatrial communication (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Confluent muscular ventricular septal defect (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Common atrioventricular-type ventricular septal defect Associated morphology True Abnormal communication Inferred relationship Some 1
Common atrioventricular-type ventricular septal defect Associated morphology True Abnormal communication Inferred relationship Some 2
Common atrioventricular canal Associated morphology True Abnormal communication Inferred relationship Some 1
Residual ventricular septal defect following procedure (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Recurrent ventricular septal defect following procedure (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Atrial septal defect due to and following acute myocardial infarction (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Ventricular septal defect due to and following infective endocarditis (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Post-infarction ventricular septal defect Associated morphology True Abnormal communication Inferred relationship Some 1
Residual interatrial communication following procedure (disorder) Associated morphology True Abnormal communication Inferred relationship Some 2
Recurrent interatrial communication following procedure (disorder) Associated morphology True Abnormal communication Inferred relationship Some 2
Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome is a rare, genetic, non-dystrophic congenital myopathy disorder characterized by a neonatal-onset of severe generalized hypotonia associated with mild psychomotor delay, congenital strabismus with abducens nerve palsy, and atrial and/or ventricular septal defects. Cryptorchidism is commonly reported in male patients and muscle biopsy typically reveals increased variability in muscle fiber size. Associated morphology True Abnormal communication Inferred relationship Some 3
Central basal perimembranous ventricular septal defect (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Ostium secundum type atrial septal defect Associated morphology True Abnormal communication Inferred relationship Some 1
Congenital atrioventricular septal defect (disorder) Associated morphology True Abnormal communication Inferred relationship Some 1
Acquired atrioventricular septal defect Associated morphology True Abnormal communication Inferred relationship Some 1
Perimembranous ventricular septal defect with extension to right ventricular inlet Associated morphology True Abnormal communication Inferred relationship Some 2
Perimembranous ventricular septal defect with extension to right ventricular trabecular component Associated morphology True Abnormal communication Inferred relationship Some 2
Perimembranous ventricular septal defect with extension to right ventricular outlet Associated morphology True Abnormal communication Inferred relationship Some 2
Perimembranous ventricular septal defect with extension to all right ventricular components (disorder) Associated morphology True Abnormal communication Inferred relationship Some 2
Perimembranous outlet ventricular septal defect with posteriorly malaligned outlet septum (disorder) Associated morphology True Abnormal communication Inferred relationship Some 2
Perimembranous inlet ventricular septal defect (disorder) Associated morphology True Abnormal communication Inferred relationship Some 2
Perimembranous inlet ventricular septal defect with atrioventricular septal malalignment (disorder) Associated morphology True Abnormal communication Inferred relationship Some 3
Perimembranous ventricular septal defect Associated morphology True Abnormal communication Inferred relationship Some 2
Central basal perimembranous ventricular septal defect (disorder) Associated morphology True Abnormal communication Inferred relationship Some 2
Perimembranous outlet ventricular septal defect with anteriorly malaligned outlet septum (disorder) Associated morphology True Abnormal communication Inferred relationship Some 3
Repair of atrial septal defect in total repair of total anomalous pulmonary venous connection Direct morphology True Abnormal communication Inferred relationship Some 1
Repair of atrial septal defect with prosthesis by open heart technique Direct morphology True Abnormal communication Inferred relationship Some 1
Repair of atrial heart septum in total repair of tetralogy of Fallot Direct morphology True Abnormal communication Inferred relationship Some 1
Closure of foramen ovale with prosthesis by closed heart technique Direct morphology True Abnormal communication Inferred relationship Some 1
Closure of foramen ovale with prosthesis by open heart technique Direct morphology True Abnormal communication Inferred relationship Some 1
Repair of ostium secundum defect with prosthesis by open heart technique Direct morphology False Abnormal communication Inferred relationship Some 3
Repair of supracristal defect with prosthesis Direct morphology True Abnormal communication Inferred relationship Some 1
Repair of ventricular septal defect in total repair of tetralogy of Fallot Direct morphology True Abnormal communication Inferred relationship Some 1
Repair of ventricular septal defect with prosthesis in total repair of tetralogy of Fallot Direct morphology True Abnormal communication Inferred relationship Some 1
Closure of ventricular septal defect with pulmonary valvotomy and patch Direct morphology False Abnormal communication Inferred relationship Some 2
Repair of ventricular septal defect with prosthesis Direct morphology True Abnormal communication Inferred relationship Some 1
Repair of heart atrial septum in total repair of truncus arteriosus Direct morphology True Abnormal communication Inferred relationship Some 1
Repair of supracristal defect with tissue graft Direct morphology False Abnormal communication Inferred relationship Some 2
Repair of ventricular septum in total repair of total anomalous pulmonary venous connection Direct morphology True Abnormal communication Inferred relationship Some 1
Repair of ostium primum defect with tissue graft Direct morphology False Abnormal communication Inferred relationship Some 2
Closure of ventricular septal defect Direct morphology True Abnormal communication Inferred relationship Some 1
Closure of septal fenestration of heart Direct morphology True Abnormal communication Inferred relationship Some 1
Repair of ostium secundum defect with tissue graft Direct morphology True Abnormal communication Inferred relationship Some 2
Repair of supracristal defect of heart Direct morphology True Abnormal communication Inferred relationship Some 1
Repair of atrial septal defect with prosthesis by closed heart technique Direct morphology True Abnormal communication Inferred relationship Some 1
Repair of ostium secundum defect Direct morphology True Abnormal communication Inferred relationship Some 1
Closure of patent foramen ovale Direct morphology True Abnormal communication Inferred relationship Some 1
Closure of ventricular septal defect with infundibular resection and patch Direct morphology True Abnormal communication Inferred relationship Some 2
Repair of ostium secundum defect with prosthesis by closed heart technique Direct morphology False Abnormal communication Inferred relationship Some 2

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