371023001: Congenital abnormal communication (morphologic abnormality)

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital abnormal communication	Is a	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital abnormal communication	Is a	Congenital malformation	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital abnormal communication	Is a	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Fused left atrioventricular valve papillary muscles	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Congenital hypoplastic left atrioventricular valve papillary muscle (disorder)	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Tetralogy of Fallot with pulmonary stenosis	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Tetralogy of Fallot with atresia of pulmonary valve	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Multiple ventricular septal defects	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Restrictive ventricular septal defect	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Perimembranous ventricular septal defect with extension to right ventricular inlet (disorder)	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Perimembranous ventricular septal defect with extension to right ventricular trabecular component	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Perimembranous ventricular septal defect with extension to right ventricular outlet (disorder)	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Perimembranous ventricular septal defect with extension to all right ventricular components (disorder)	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Ventricular septal defect with malaligned outlet septum to right	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Ventricular septal defect with malaligned outlet septum to right overriding aortic valve	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Ventricular septal defect with malaligned outlet septum to right overriding pulmonary valve	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Ventricular septal defect with malaligned outlet septum to left	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Ventricular septal defect with malaligned outlet septum to left overriding aortic valve	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Ventricular septal defect with malaligned outlet septum to left overriding pulmonary valve	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Ventricular septal defect with malaligned outlet septum and overriding truncal valve (disorder)	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Muscular ventricular septal defect in inlet septum	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Muscular ventricular septal defect in central trabecular septum (disorder)	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Muscular ventricular septal defect in apical trabecular septum	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Muscular ventricular septal defect in marginal septum	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Muscular ventricular septal defect in outlet septum	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Doubly committed subarterial ventricular septal defect	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Doubly committed subarterial ventricular septal defect with membranous septum extension	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Doubly committed subarterial ventricular septal defect with muscular posterior inferior rim (disorder)	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Giant ventricular septal defect	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Abnormal infundibular morphology	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Subpulmonary infundibulum (disorder)	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Subaortic infundibulum (disorder)	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Bilateral muscular infundibula	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Bilateral deficient infundibula	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Ventricular septal aneurysm (disorder)	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Type II common arterial trunk	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Pleuropericardial cyst	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Spontaneous closure of ventricular septal defect (finding)	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Ventricular septal defect, repaired	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Common atrioventricular canal	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Endocardial cushion defect	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Aortic septal defect	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Ostium primum defect	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Aortic left ventricular tunnel	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Ventricular septal defect	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Abnormal communication between pericardial sac and pleura	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Sinus pericranii	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Common arterial trunk and separate origin of pulmonary arteries (disorder)	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Atrial septal defect with endocardial cushion defect, partial type (disorder)	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Common truncus arteriosus (disorder)	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital bronchopulmonary foregut malformation	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital bronchopulmonary foregut malformation	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Truncus arteriosus, Edwards' type I	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Double outlet right ventricle	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Roger's disease	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Eisenmenger's defect	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Common arterial trunk and widely separate origin of pulmonary arteries	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Tetralogy of Fallot	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Abnormal communication between pericardial sac and peritoneal cavity	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Membranous ventricular septum defect	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Muscular ventricular septum defect	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Pentalogy of Fallot	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Interventricular septal defect	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Stenosis of infundibulum of right ventricle (disorder)	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Dextraposition of aorta in Fallot's tetralogy	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Ventricular septal defect in Fallot's tetralogy (disorder)	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Common aortopulmonary trunk NOS	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Double outlet right ventricle, unspecified	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Double outlet right ventricle NOS	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Tetralogy of Fallot NOS	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Ventricular septal defect, unspecified	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Other specified ventricular septal defect	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Ventricular septal defect NOS	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Tetralogy of Fallot, unspecified	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Congenital bronchopulmonary foregut malformation	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital bronchopulmonary foregut malformation	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital septal defect	Is a	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital valvular insufficiency	Is a	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital bronchopulmonary foregut malformation	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Tetralogy of Fallot with pulmonary stenosis	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Tetralogy of Fallot with atresia of pulmonary valve	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Atrial septal defect with endocardial cushion defect, partial type (disorder)	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Tetralogy of Fallot	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Pentalogy of Fallot	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Dextraposition of aorta in Fallot's tetralogy	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Ventricular septal defect in Fallot's tetralogy (disorder)	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	6
Tetralogy of Fallot NOS	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Tetralogy of Fallot, unspecified	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Tetralogy of Fallot with absent pulmonary valve	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Congenital bronchopulmonary foregut malformation	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Endocardial cushion defects, unspecified	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Other specified endocardial cushion defects	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Endocardial cushion defects NOS	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital bronchopulmonary foregut malformation	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital bronchopulmonary foregut malformation	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Patent processus vaginalis (disorder)	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital hiatus hernia	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Patent vitelline duct (disorder)	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital bronchopulmonary foregut malformation	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital bronchopulmonary foregut malformation	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital bronchopulmonary foregut malformation	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital bronchopulmonary foregut malformation	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital bronchopulmonary foregut malformation	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital bronchopulmonary foregut malformation	Associated morphology	False	Congenital abnormal communication	Inferred relationship	Existential restriction modifier (core metadata concept)	2

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Reference Sets

Concept inactivation indicator attribute value reference set (foundation metadata concept)

SAME AS association reference set (foundation metadata concept)

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Id	Description	Lang	Type	Status	Case?	Module
1196319016	Congenital abnormal communication (morphologic abnormality)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1209734013	Congenital abnormal communication	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1228912018	Anomalous congenital connection	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1196319016	Congenital abnormal communication (morphologic abnormality)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1196319016	Congenital abnormal communication (morphologic abnormality)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1209734013	Congenital abnormal communication	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1209734013	Congenital abnormal communication	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1228912018	Anomalous congenital connection	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1228912018	Anomalous congenital connection	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core