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74175007: Congenital abnormal communication (morphologic abnormality)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    123176016 Congenital abnormal communication en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    123181013 Anomalous congenital connection en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    123182018 Congenital abnormal origin en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    123183011 Congenital abnormal insertion en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    814645012 Congenital abnormal communication (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    123176016 Congenital abnormal communication en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    123176016 Congenital abnormal communication en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    123181013 Anomalous congenital connection en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    123181013 Anomalous congenital connection en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    123182018 Congenital abnormal origin en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    123182018 Congenital abnormal origin en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    123183011 Congenital abnormal insertion en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    123183011 Congenital abnormal insertion en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    814645012 Congenital abnormal communication (morphologic abnormality) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    814645012 Congenital abnormal communication (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

    0 descendants.

    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)
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Left atrioventricular valve chordae too short (disorder) Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept)
    Left atrioventricular valve chordae too long Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept)
    Left atrioventricular valve chordae to outlet septum (disorder) Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept)
    Arcade abnormality of left atrioventricular valve chordae Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept)
    Congenital abnormality of left atrioventricular valve papillary muscle (disorder) Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept)
    Congenital parachute malformation of left atrioventricular valve Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept)
    Congenital absence of left atrioventricular valve papillary muscle Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept)
    Fused left atrioventricular valve papillary muscles Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept)
    Congenital hypoplastic left atrioventricular valve papillary muscle (disorder) Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept)
    Tetralogy of Fallot with pulmonary stenosis Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 15
    Tetralogy of Fallot with atresia of pulmonary valve Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 15
    Multiple ventricular septal defects Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 15
    Restrictive ventricular septal defect Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 15
    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) 15
    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) 15
    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) 15
    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) 15
    Muscular ventricular septal defect in inlet septum Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 15
    Muscular ventricular septal defect in central trabecular septum (disorder) Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 15
    Muscular ventricular septal defect in apical trabecular septum Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 15
    Muscular ventricular septal defect in marginal septum Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 15
    Muscular ventricular septal defect in outlet septum Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 15
    Doubly committed subarterial ventricular septal defect Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 15
    Giant ventricular septal defect Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 15
    Abnormal infundibular morphology Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 15
    Ventricular septal aneurysm (disorder) Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 15
    Type II common arterial trunk Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept)
    Pleuropericardial cyst Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept)
    Spontaneous closure of ventricular septal defect (finding) Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 15
    Ventricular septal defect, repaired Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 15
    Congenital pulmonary vein confluence (disorder) Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept)
    Congenital pulmonary artery conduit Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept)
    Common atrioventricular canal Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept)
    Endocardial cushion defect Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept)
    Aortic septal defect Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept)
    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)
    Ventricular septal defect Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 15
    Abnormal communication between pericardial sac and pleura Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept)
    Sinus pericranii Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept)
    Common arterial trunk and separate origin of pulmonary arteries (disorder) Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept)
    Common truncus arteriosus (disorder) Associated morphology 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)
    Truncus arteriosus, Edwards' type I Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept)
    Double outlet right ventricle Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 15
    Velamentous insertion of umbilical cord Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 1
    Roger's disease Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 15
    Eisenmenger's defect Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 1
    Common arterial trunk and widely separate origin of pulmonary arteries Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept)
    Tetralogy of Fallot Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 15
    Abnormal communication between pericardial sac and peritoneal cavity Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept)
    Membranous ventricular septum defect Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 15
    Muscular ventricular septum defect Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 15
    Pentalogy of Fallot Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 15
    Interventricular septal defect Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 15
    Stenosis of infundibulum of right ventricle (disorder) Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 15
    Ventricular septal defect in Fallot's tetralogy (disorder) Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 15
    Atrial septal defect with endocardial cushion defect, partial type (disorder) Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept)
    Common aortopulmonary trunk NOS Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept)
    Double outlet right ventricle, unspecified Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 15
    Double outlet right ventricle NOS Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 15
    Tetralogy of Fallot NOS Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 15
    Ventricular septal defect, unspecified Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 15
    Other specified ventricular septal defect Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 15
    Ventricular septal defect NOS Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 15
    Tetralogy of Fallot, unspecified Associated morphology False Congenital abnormal communication Inferred relationship Existential restriction modifier (core metadata concept) 15

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    Reference Sets

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

    POSSIBLY EQUIVALENT TO association reference set

    SAME AS association reference set (foundation metadata concept)

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